Aqueous lubricant and surface conditioner for formed metal surfaces

BACKGROUND OF THE INVENTION
1. Field of the Invention
This invention relates to processes and compositions which accomplish at least one, and most preferably all, of the following related objectives when applied to formed metal surfaces, more particularly to the surfaces of aluminum and/or tin plated cans, either after cleaning or as a pan of cleaning: (i) reducing the coefficient of static friction of the treated surfaces after drying of such surfaces, without adversely affecting the adhesion of paints or lacquers applied thereto; (ii) promoting the drainage of water from treated surfaces, without causing "water-breaks", i.e., promoting drainage that results in a thin, continuous film of water on the cans, instead of distinct water droplets separated by the relatively dry areas called "water-breaks" between the water droplets; and (iii) lowering the dryoff oven temperature required for drying said surfaces after they have been rinsed with water.
2. Discussion of Related Art
The following discussion and the description of the invention will be set forth primarily for aluminum cans, as these represent the largest volume area of application of the invention. However, it is to be understood that, with the obviously necessary modifications, both the discussion and the description of the invention apply also to tin plated steel cans and to other types of formed metal surfaces for which any of the above stated intended purposes of the invention is practically interesting.
Aluminum cans are commonly used as containers for a wide variety of products. After their manufacture, the aluminum cans are typically washed with acidic cleaners to remove aluminum fines and other contaminants therefrom. Recently, environmental considerations and the possibility that residues remaining on the cans following acidic cleaning could influence the flavor of beverages packaged in the cans has led to an interest in alkaline cleaning to remove such fines and contaminants. However, the treatment of aluminum cans with either alkaline or acidic cleaners generally results in differential rates of metal surface etch on the outside versus on the inside of the cans. For example, optimum conditions required to attain an aluminum fine-free surface on the inside of the cans usually leads to can mobility problems on conveyors because of the increased roughness on the outside can surface.
Aluminum cans that lack a low coefficient of static friction (hereinafter often abbreviated as "COF") on the outside surface usually do not move past each other and through the trackwork of a can plant smoothly. Clearing the jams resulting from failures of smooth flow is inconvenient to the persons operating the plant and costly because of lost production. The COF of the internal surface is also important when the cans are processed through most conventional can decorators. The operation of these machines requires cans to slide onto a rotating mandrel which is then used to transfer the can past rotating cylinders which transfer decorative inks to the exterior surface of the cans. A can that does not slide easily on or off the mandrel can not be decorated properly and results in a production fault called a "printer trip". In addition to the misloaded can that directly causes such a printer trip, three to four cans before and after the misloaded one are generally lost as a consequence of the mechanics of the printer and conveyor systems. Jams and printer trips have become increasingly troublesome problems as line speed have increased during recent years to levels of about 1200 to 1500 cans per minute that are now common. Thus, a need has arisen in the can manufacturing industry, particularly with aluminum cans, to modify the COF on the outside and inside surfaces of the cans to improve their mobility.
An important consideration in modifying the surface properties of cans is the concern that such modification may interfere with or adversely affect the ability of the can to be printed when passed to a printing or labeling station. For example, after cleaning the cans, labels may be printed on their outside surface, and lacquers may be sprayed on their inside surface. In such a case, the adhesion of the paints and lacquers is of major concern. It is therefore an object of this invention to improve mobility without adversely affecting adhesion of paints, decorating inks, lacquers, or the like.
In addition, the current trend in the can manufacturing industry is directed toward using thinner gauges of aluminum metal stock. The down-gauging of aluminum can metal stock has caused a production problem in that, after washing, the cans require a lower drying oven temperature in order to pass the column strength pressure quality control test. However, lowering the drying oven temperature resulted in the cans not being dry enough when they reached the printing station, and caused label ink smears and a higher rate of can rejects.
One means of lowering the drying oven temperature would be to reduce the amount of water remaining on the surface of the cans after water rinsing. Thus, it is advantageous to promote the drainage of rinse water from the treated can surfaces. However, in doing so, it is generally important to prevent the formation of surfaces with water-breaks as noted above. Such water-breaks give rise to at least a perception, and increase the possibility in reality, of non-uniformity in practically important properties among various areas of the surfaces treated.
Thus, it is desirable to provide a means of improving the mobility of aluminum cans through single filers and printers to increase production, reduce line jammings, minimize down time, reduce can spoilage, improve or at least not adversely affect ink laydown, and enable lowering the drying oven temperature of washed cans.
In the most widely used current commercial practice, at least for large scale operations, aluminum cans are typically subjected to a succession of six cleaning and rinsing operations as described in Table 1 below. (Contact with ambient temperature tap water before any of the stages in Table 1 is sometimes used also; when used, this stage is often called a "vestibule" to the numbered stages.) Preferably, at least the operations described in Stages 1, 2, 3, and 6 from Table 1 are used in practice; stage 1 may be omitted, but the results usually are less satisfactory than when it is included.
TABLE 1______________________________________STAGENUMBER ACTION ON SURFACE DURING STAGE______________________________________1 Aqueous Acid Precleaning2 Aqueous Acid or Alkali and Surfactant Cleaning3 Water Rinse4 Mild Acid Postcleaning, Conversion Coating, or Water Rinse5 Water Rinse6 Deionized ("DI") Water Rinse______________________________________
It is currently possible to produce a can which is satisfactorily mobile and to which subsequently applied inks and/or lacquers have adequate adhesion by using suitable surfactants either in Stage 4 or Stage 6 as noted above. Preferred treatments for use in Stage 6 are described in U.S. Pat. Nos. 4,944,889 and 4,859,351, and some of them are commercially available from the Parker Amchem Division of Henkel Corporation (hereinafter often abbreviated as "PA") under the name "Mobility Enhancer.TM. 40" (herein often abbreviated "ME-40.TM.").
However, many manufacturers have been found to be reluctant to use chemicals such as ME-40.TM. in Stage 6. In some cases, this reluctance is due to the presence of a carbon filter for the DI water (normal Stage 6) system, a filter that can become inadequately effective as a result of adsorption of lubricant and surface conditioner forming additives such as those in ME-40.TM.; in other cases, it is due to a reluctance to make the engineering changes necessary to run ME-40.
For those manufacturers that prefer not to add any lubricant and surface conditioner material to the final stage of rinsing but still wish to achieve the advantages that can be obtained by such additions, alternative treatments for use in Stage 4 as described above have been developed and are described in U.S. Pat. Nos. 5,030,323 and 5,064,500. Some of these materials are commercially available from PA under the name FIXO-DINE.TM. 500.
However, the reduction in coefficient of friction provided by prior art treatments in either Stage 4 or Stage 6 can be substantially reduced, often to an unacceptable level, if the treated cans are subjected to extraordinary heating after completion of the six process stages described above. Such extraordinary heating of the cans in the drying oven occurs whenever a high speed production line is stalled for even a few minutes, an event that is by no means rare in practice. In practical terms, the higher COF measurements correlate with the loss of mobility, thereby defeating the purpose of introducing mobility enhancing surfactants into can washing formulations. Accordingly, it is an object of this invention to provide means, of improving the mobility of aluminum cans and/or achieving one of the other objects stated above, that are superior to means taught in the prior art, particularly with respect to stability of the beneficial effects to heating well beyond the minimum extent necessary for drying the treated surfaces.
Also, some beverages packaged in aluminum cans are pasteurized, and unless the temperature and the composition(s) of the aqueous solution(s) with which cans are contacted during pasteurization are very carefully controlled, staining of the dome of the can often occurs during pasteurization. It is a further object of some embodiments of this invention to provide compositions and methods suitable for use in reducing coefficient of friction that will also resist such dome staining during pasteurization.
Still another object of some embodiments of this invention is to provide a combination alkaline cleaner and mobility enhancer, so that no addition of a mobility enhancing ingredient is required after Stage 2 as described above. In a particularly preferred embodiment, this is accomplished with cleaning ingredients that are substantially free from fluoride in any stage of cleaning.
DESCRIPTION OF THE INVENTION
Other than in the operating examples, or where otherwise indicated, all numbers expressing quantities of ingredients or reaction conditions used herein are to be understood as modified in all instances by the term "about" in describing the broadest scope of the invention. Practice within the numerical limits given, however, is generally preferred.
Also, unless there is an explicit statement to the contrary, the description below of groups of chemical materials as suitable or preferred for a particular ingredient according to the invention implies that mixtures of two or more of the individual group members are equally as suitable or preferred as the individual members of the group used alone. Furthermore, the specification of chemical materials in ionic form should be understood as implying the presence of some counterions as necessary for electrical neutrality of the total composition. In general, such counterions should first be selected to the extent possible from the ionic materials specified as part of the invention; any remaining counterions needed may generally be selected freely, except for avoiding any counterions that are detrimental to the objects of the invention.
SUMMARY OF THE INVENTION
In accordance with this invention, it has been found that a lubricant and surface conditioner applied to aluminum cans after washing enhances their mobility and, in a preferred embodiment, improves their water film drainage and evaporation characteristics as to enable lowering the temperature of a drying oven by from about 25.degree. to about 38.degree. C. without having any adverse effect on the label printing process. The lubricant and surface conditioner reduces the coefficient of static friction on the outside surface of the cans, enabling a substantial increase in production line speeds, and in addition, provides a noticeable improvement in the rate of water film drainage and evaporation resulting in savings due to lower energy demands while meeting quality control requirements.
Various embodiments of the invention include a concentrated lubricant and surface conditioner forming composition as described above; a solution of such a composition in water, optionally with additional acid or base to adjust the pH value, suitable as the complete composition for contacting a metal surface, in Stage 2, Stage 4, and/or Stage 6 of a six stage cleaning and rinsing process as described above; and processes including contacting a metal surface, particularly an aluminum surface, with an aqueous composition including the ingredients of any lubricant and surface conditioner forming composition specified in detail above.

BRIEF DESCRIPTION OF THE DRAWINGS
FIGS. 1(a)-1(d) illustrate the effect of fluoride activity during cleaning of cans before applying a lubricant and surface conditioner according to this invention on the characteristics of the cans after processing.

DESCRIPTION OF PREFERRED EMBODIMENTS
More particularly, in accordance with one preferred embodiment of this invention, it has been found that application of a thin organic film to the outside surface of aluminum cans serves as a lubricant inducing thereto a lower coefficient of static friction, which consequently provides an improved mobility to the cans, and also increases the rate at which the cans may be dried and still pass the quality control column strength pressure test. It has also been found that the degree of improved mobility and drying rate of the cans depends on the thickness or amount of the organic film, and on the chemical nature of the material applied to the cans.
The lubricant and surface conditioner for aluminum cans in accordance with this invention may, for example, be selected from water-soluble alkoxylated surfactants such as organic phosphate esters; alcohols; fatty acids including mono-, di-, tri-, and poly-acids; fatty acid derivatives such as salts, hydroxy acids, amides, esters, particularly alkyl esters of 2-substituted alkoxylated fatty alkyloxy acetic acids (briefly denoted hereinafter as "oxa-acid esters") as described more fully in U.S. application Ser. No. 843,135 filed Feb. 28, 1992; ethers and derivatives thereof; and mixtures thereof.
The lubricant and surface conditioner for aluminum cans in accordance with this invention in one embodiment preferably comprises a water-soluble derivative of a saturated fatty acid such as an ethoxylated stearic acid or an ethoxylated isostearic acid, or alkali metal salts thereof such as polyoxyethylated stearate and polyoxyethylated isostearate. Alternatively, the lubricant and surface conditioner for aluminum cans may comprise a water-soluble alcohol having at least about 4 carbon atoms and may contain up to about 50 moles of ethylene oxide. Excellent results have been obtained when the alcohol comprises polyoxyethylated oleyl alcohol containing an average of about 20 moles of ethylene oxide per mole of alcohol.
In another preferred aspect of this invention, the organic material employed to form a film on an aluminum can following alkaline or acid cleaning and prior to the last drying of the exterior surface prior to conveying comprises a water-soluble organic material selected from a phosphate ester, an alcohol, fatty acids including mono-, di-, tri-, and poly-acids fatty acid derivatives including salts, hydroxy acids, amides, alcohols, esters, ethers and derivatives thereof and mixtures thereof. Such organic material is preferably part of an aqueous solution comprising water-soluble organic material suitable for forming a film on the cleaned aluminum can to provide the surface after drying with a coefficient of static friction not more than 1.5 and that is less than would be obtained on a can surface of the same type without such film coating.
In one embodiment of the invention, water solubility can be imparted to organic materials by alkoxylation, preferably ethoxylation, propoxylation or mixture thereof. However, non-alkoxylated phosphate esters are also useful in the present invention, especially free acid containing or neutralized mono-and diesters of phosphoric acid with various alcohols. Specific examples include Tryfac.TM. 5573 Phosphate Ester, a free acid containing ester available from Henkel Corp.; and Triton.TM. H-55, Triton.TM. H-66, and Triton.TM. QS-44, all available from Union Carbide Corp.
Preferred non-ethoxylated alcohols include the following classes of alcohols:
Suitable monohydric alcohols and their esters with inorganic acids include water soluble compounds containing from 3 to about 20 carbons per molecule. Specific examples include sodium lauryl sulfates such as Duponol.TM. WAQ and Duponol.TM. QC and Duponol.TM. WA and Duponol.TM. C available from Witco Corp. and proprietary sodium alkyl sulfonates such as Alkanol.TM. 189-S available from E.I. du Pont de Nemours & Co.
Suitable polyhydric alcohols include aliphatic or arylalkyl polyhydric alcohols containing two or more hydroxyl groups. Specific examples include glycerine, sorbitol, mannitol, xanthan gum, hexylene glycol, gluconic acid, gluconate salts, glucoheptonate salts, pentaery-thritol and derivatives thereof, sugars, and alkylpolyglycosides such as APG.TM. 300 and APG.TM. 325, available from Henkel Corp. Especially preferred polyhydric alcohols include triglycerols, especially glycerine or fatty acid esters thereof such as castor oil triglycerides.
In accordance with the present invention, we have discovered that employing alkoxylated, especially ethoxylated, castor oil triglycerides as lubricants and surface conditioners results in further improvements in can mobility especially where operation of the can line is interrupted, causing the cans to be exposed to elevated temperatures for extended periods. Accordingly, especially preferred materials include Trylox.TM. 5900, Trylox.TM. 5902, Trylox.TM. 5904, Trylox.TM. 5906, Trylox.TM. 5907, Trylox.TM. 5909, Trylox.TM. 5918, and hydrogenated castor oil derivatives such as Trylox.TM. 5921 and Trylox.TM. 5922, all available from Henkel Corp.
Preferred fatty acids include butyric, valeric, caproic, caprylic, capric, pelargonic, lauric, myristic, palmitic, oleic, stearic, linoleic, and ricinoleic acids; malonic, succinic, glutaric, adipic, maleic, tartaric, gluconic, and dimer acids; and salts of any of these; iminodipropionate salts such as Amphoteric N and Amphoteric 400 available from Exxon Chemical Co.; sulfosuccinate derivatives such as Texapon.TM. SH-135 Special and Texapon.TM. SB-3, available from Henkel Corp.; citric, nitrilotriacetic, and trimellitic acids; Versenol.TM. 120 HEEDTA, N-(hydroxyethyl)ethylenediaminetriacetate, available from Dow Chemical Co.
Preferred amides generally include amides or substituted amides of carboxylic acids having from four to twenty carbons. Specific examples are Alkamide.TM. L203 lauric monoethanolamide, Alkamide.TM. L7DE lauric/myristic alkanolamide, Alkamide.TM. DS 280/s stearic diethanolamide, Alkamide.TM. CD coconut diethanolamide, Alakamide.TM. DIN 100 lauric/linoleic diethanolamide, Alkamide.TM. DIN 295/s linoleic diethanolamide, Alkamide.TM. DL 203 lauric diethanolamide, all available from Rhone-Poulenc; Monamid.TM. 150-MW myristic ethanolamide, Monamid.TM. 150-CW capric ethanolamide, Monamid.TM. 150-IS isostearic ethanolamide, all available from Mona Industries Inc.; and Ethomid.TM. HT/23 and Ethomid.TM. HT60 polyoxyethylated hydrogenated tallow amines, available from Akzo Chemicals Inc.
Preferred anionic organic derivatives generally include sulfate and sulfonate derivatives of fatty acids including sulfate and sulfonate derivatives of natural and synthetically derived alcohols, acids and natural products. Specific Examples: dodecyl benzene sulfonates such as Dowfax.TM. 2A1, Dowfax.TM. 2A0, Dowfax.TM. 3B0, and Dowfax.TM. 3B2, all available from Dow Chemical Co.; Lomar.TM. LS condensed naphthalene sulfonic acid, potassium salt available from Henkel Corp.; sulfosuccinate derivatives such as Monamate.TM. CPA sodium sulfosuccinate of a modified alkanolamide, Monamate.TM. LA-100 disodium lauryl sulfosuccinate, all available from Mona Industries; Triton.TM. GR-SM sodium dioctylsulfosuccinate, available from Union Carbide Chemical and Plastics Co.; Varsulf.TM. SBFA 30, fatty alcohol ether sulfosuccinate, Varsulf.TM. SBL 203, fatty acid alkanolamide sulfosuccinate, Varsulf.TM. S1333, ricinoleic monoethanolamide sulfosuccinate, all available from Witco Chemical Co.
Another preferred group of organic materials comprise water-soluble alkoxylated, preferably ethoxylated, propoxylated, or mixed ethoxylated and propoxylated materials, most preferably ethoxylated, and non-ethoxylated organic materials selected from amine salts of fatty acids including mono-, di-, tri-, and poly-acids, amino fatty acids, fatty amine N-oxides, and quaternary salts, and water soluble polymers.
Preferred amine salts of fatty acids include ammonium, quaternary ammonium, phosphonium, and alkali metal salts of fatty acids and derivatives thereof containing up to 50 moles of alkylene oxide in either or both the cationic or anionic species. Specific examples include Amphoteric N and Amphoteric 400 iminodipropionate sodium salts, available from Exxon Chemical Co.; Deriphat.TM. 154 disodium N-tallow-beta iminodipropionate and Deriphat.TM. 160, disodium N-lauryl-beta iminodipropionate, available from Henkel Corp.
Preferred amino acids include alpha and beta amino acids and diacids and salts thereof, including alkyl and alkoxyiminodipropionic acids and their salts and safcosine derivatives and their salts. Specific examples include Armeen.TM. Z, N-coco-beta-aminobutyric acid, available from Akzo Chemicals Inc.; Amphoteric N, Amphoteric 400, Exxon Chemical Co.; sarcosine (N-methyl glycine); hydroxyethyl glycine; Hamposyl.TM. TL-40 triethanolamine lauroyl sarcosinate, Hamposyl.TM. O oleyl sarcosinate, Hamposyl.TM. AL-30 ammoniumlauroyl sarcosinate, Hamposyl.TM. L lauroyl sarcosinate, and Hamposyl.TM. C cocoyl sarcosinate, all available from W.R. Grace & Co.
Preferred amine N-oxides include amine oxides where at least one alkyl substituent contains at least three carbons and up to 20 carbons. Specific examples include Aromox.TM. C/12 bis-(2-hydroxyethyl)cocoalkylamine oxide, Aromox.TM. T/12 bis-(2-hydroxyethyl)tallowalkyl oxide, Aromox.TM. DMC dimethylcocoalkylamine oxide, Aromox.TM. DMHT hydrogenated dimethyltallowalkylamine oxide, Aromox.TM. DM-16 dimethylheaxdecylalkylamine oxide, all available from Akzo Chemicals Inc.; and Tomah.TM. AO-14-2 and Tomah.TM. AO-728 available from Exxon Chemical Co.
Preferred quaternary salts include quaternary ammonium derivatives of fatty amines containing at least one substituent containing from 12 to 20 carbon atoms and zero to 50 moles of ethylene oxide and/or zero to 15 moles of propylene oxide where the counter ion consists of halide, sulfate, nitrate, carboxylate, alkyl or aryl sulfate, alkyl or aryl sulfonate or derivatives thereof. Specific examples include Arquad.TM. 12-37W dodecyltrimethylammonium chloride, Arquad.TM. 18-50 octadecyltrimethylammonium chloride, Arquad.TM. 210-50 didecyldimethylammonium chloride, Arquad.TM. 218-100 dioctadecyldimethylammonium chloride, Arquad.TM. 316(W) trihexadecylmethylammonium chloride, Arquad.TM. B-100 benzyldimethyl(C.sub.12-18)alkylammonium chloride, Ethoquad.TM. C/12 cocomethyl[POE(2)]ammonium chloride, Ethoquad.TM. C/25 cocomethyl[POE(15)]ammonium chloride, Ethoquad.TM. C/12 nitrate salt, Ethoquad.TM. T/13 Acetate tris(2-hydroxyethyl)tallowalkyl ammonium acetate, Duoqaud.TM. T-50 N,N,N',N',N'-pentamethyl-N-tallow-1,3-diammonium dichloride, Propoquad.TM. 2HT/11 di(hydrogenated tallowalkyl)(2-hydroxy-2-methylethyl)methylammonium chloride, Propoquad.TM. T/12 tallowalkylmethyl-bis-(2-hydroxy-2-methylethyl)ammonium methyl sulfate, all available from Akzo Chemicals Inc.; Monaquat.TM. P-TS stearamidopropyl PG-diammonium chloride phosphate, available from Mona Industries Inc.; Chemquat.TM. 12-33 lauryltrimethylammonium chloride, Chemquat.TM. 16-50 Cetyltrimethylammonium chloride available from Chemax Inc.; and tetraethylammonium pelargonate, laurate, myristate, oleate, stearate or isostearate.
A combination of fluoride ions with either amine oxide or quaternary ammonium salts as described above, preferably the latter, is a major part of one especially preferred embodiment of the invention when good resistance of the friction reduction to overheating and/or resistance to dome staining during pasteurization is needed. More particularly, a suitable additive to satisfy these objectives preferably comprises, more preferably consists essentially of, or still more preferably consists of:
(A) a component selected from the group consisting of quaternary ammonium salt and amine oxide surfactants conforming to general formula I: ##STR1## where R.sup.1 is a monovalent aliphatic moiety, which may be saturated or unsaturated and contains from 8 to 22 carbon atoms, or preferably from 12 to 18 carbon atoms, preferably arranged in a straight chain; each of R.sup.2 and R.sup.3 is a monovalent moiety independently selected from the group consisting of (i) alkyl and hydroxyalkyl moieties having from 1 to 8, preferably from 1 to 4, more preferably 1 or 2, carbon atoms and (ii) aryl and arylalkyl moieties having from 6 to 10, or preferably from 6 to 8, carbon atoms; R.sup.4 is a monovalent moiety selected from the same group as for R.sup.2 and R.sup.3 plus the --O.sup.- moiety; X.sup.- is a monovalent anion or monovalent fraction of an anion with a valence higher than 1; and a=0 if R.sup.4 is --O.sup.-, and a=1 if R.sup.4 is not --O.sup.- ;
(B) a component of complex fluoride anions, with anions selected from the group consisting of fluotitanate, fluohafnate, and fluozirconate preferred and fluozirconate alone most preferred; and, optionally but preferably,
(C) a component selected from the group consisting of phosphate, sulfate, and nitrate ions, with phosphate or a mixture of phosphate with one or both of sulfate and nitrate preferred; and, optionally,
(D) aluminate anions, including fluoroaluminate anions; and, optionally
(E) aluminum cations, including complex fluoroaluminum cations, and, optionally, one or both of:
(F) a water soluble and/or water dispersible polymer including amino-substituted vinyl phenolic moieties, as described in detail in one or more of U.S. Pat. Nos. 5,116,912, 5,068,299, 5,063,089, 4,944,812, 4,517,028, 4,457,790, 4,433,015, and 4,376,000; and
(G) a foam reducing (antifoam) component.
For component (A) as defined above, quaternary salts are preferred over amine oxides when dome staining resistance is desired. Independently, it is preferred that at least two, or more preferably all three, of the moieties R.sup.2, R.sup.3, and R.sup.4 be hydroxyalkyl groups, most preferably 2-hydroxyethyl groups. For economy and commercial availability, it is preferred that the R.sup.1 moieties in the materials used for component (A) be mixtures of the alkyl groups corresponding to the mixture of alkyl groups present in the fatty acid mixtures derived from hydrolysis of natural fats and oils, such as coconut oil, palm kernel oil, animal tallow, and the like. Alkyl groups from animal tallow are particularly preferred.
For component (B), fluozirconate ions added as fluozirconic acid are most preferred. The optimal amount of fluoride can conveniently be monitored during use if desired by means of a fluoride sensitive electrode as described in U.S. Pat. No. 3,431,182 and commercially available from Orion Instruments. "Fluoride activity" as this term is used herein was measured relative to a 120E Activity Standard Solution, commercially available from the PA, by a procedure described in detail in PA Technical Process Bulletin No. 968. The Orion Fluoride Ion Electrode and the reference electrode provided with the Orion instrument are both immersed in the noted Standard Solution and the millivolt meter reading is adjusted to 0 with a Standard Knob on the instrument, after waiting if necessary for any initial drift in readings to stabilize. The electrodes are then rinsed with deionized or distilled water, dried, and immersed in the sample to be measured, which should be brought to the same temperature as the noted Standard Solution had when it was used to set the meter reading to 0. The reading of the electrodes immersed in the sample is taken directly from the millivolt (hereinafter often abbreviated "mv") meter on the instrument. With this instrument, lower positive mv readings indicate higher fluoride activity, and negative mv readings indicate still higher fluoride activity than any positive readings, with negative readings of high absolute value indicating high fluoride activity.
The initial millivolt reading of a well operating freshly prepared working composition according to this embodiment of the invention ideally should be at least approximately maintained throughout the use of the composition. The mv reading for free fluoride activity in such a working composition according to this embodiment of the invention, including components (A), (B), and (C) as defined above, preferably should lie, with increasing preference in the order given, within the range from -30 to -120, -50 to -100, -60 to -85, -68 to -80, or -68 to -72, mv.
The anions specified for component (C) above are preferably added to the mixtures according to the invention in the form of the corresponding acids. When resistance to dome staining is desired, component (C) preferably includes phosphate anions. Because of the preferred values for pH and for the ratio of the phosphate content of component (C) to components (A) and (B) when component (C) includes phosphate, which are considered further below, usually some other acid than phosphoric acid is required to bring the pH within the preferred ranges without exceeding the preferred ratio of phosphate to the other components. In such cases, nitric acid is preferably used when dome staining resistance is desired; otherwise, any other sufficiently strong acid that does not interfere with the attainment of the objects of the invention may be used; in such cases, sulfuric acid is normally preferred primarily because it is less expensive than other strong acids.
Components (D) and (E) normally are not added deliberately to the stage 4 composition (except for testing purposes), but normally accumulate in it as it is used under practical conditions for treating aluminum surfaces. While aluminum is unlikely to have any beneficial effect, experience has indicated that a normal equilibrium concentration in commercial aluminum can cleaning lines will be within the range from 100-300 parts per million by weight (hereinafter often abbreviated "ppm"), and satisfactory results can be obtained with compositions including this much, or even more, aluminum. Preferably the total concentration of components (D) and (E) is, with increasing preference in the order given, not more than 1000, 700, 500, 450, 400, 370, 340, 325, or 315 ppm.
In a complete Stage 4 working composition according to the embodiments of this invention including amine oxide or quaternary ammonium salts as a necessary component, the pH is preferably maintained in the range from 2.3 to 3.3, more preferably from 2.5 to 3.1, still more preferably from 2.70 to 2.90. Values of pH lower than those stated usually result in less resistance than is desirable to dome staining, while pH values higher than those stated tend to result in inadequate etching of the surface to assure good adhesion of subsequently applied lacquers and/or inks. Addition of acid during prolonged operation is generally required to maintain these values of pH, because acidity is consumed by the process that forms the lubricant and surface conditioner coating. If the surfaces being treated are predominantly aluminum as is most common, it is preferable to include in the replenishment acid, which is added during prolonged use of the lubricant and surface conditioner forming composition, a sufficient amount of hydrofluoric acid to complex the aluminum dissolved into the lubricant and surface conditioner forming composition during its use.
When component (C) includes phosphate ions as is generally preferred, the molar ratio between components (C.sub.P):(B):(A), where "C.sub.P " denotes the phosphate content only of component (C) as defined above, is preferably, with increasing preference in the order given, in the range from 1.0:(0.5-4.0):(0.25-8.0), 1.0:(0.5-2.0):(0.5-6.0), 1.0:(0.7-1.3):(0.8-1.5), 1.0:(0.8-1.2):(0.90-1.40), 1.0:(0.90-1.10):(1.05-1.25), or 1.0:(0.95-1.05):(1.05-1.15). If component (C) is not used or does not contain phosphate, the ratio of (B):(A), with respect to those two components, preferably falls within the same ranges as stated above for cases in which phosphate is included in the compositions. Independently, the concentration of component (A) in a working Stage 4 composition preferably is, with increasing preference in the order given, in the range from 0.14 to 2.25, 0.42 to 1.50, 0.56 to 1.12, 0.67 to 0.98, or 0.77 to 0.88, millimoles per liter (hereinafter often abbreviated "mM"); the concentration of component (B) in a working Stage 4 composition preferably is in the range from 0.20 to 2.0, or more preferably from 0.40 to 1.0, mM; and the concentration of component (C.sub.P) in a working Stage 4 composition preferably is in the range from 0.20 to 2.0, more preferably from 0.40 to 1.0, or still more preferably from 0.60 to 0.84, mM. [In these numerical specifications, for component (C.sub.P), the stoichiometric equivalent as phosphate ion of any unionized phosphoric acid or anions produced by any degree of ionization of phosphoric acid is to be considered as phosphate anions.]
Higher concentrations of component (A) within the stated ranges improve the dome staining resistance during pasteurization but also increase the foaming tendency of the composition and often must be avoided for that reason. The lower the concentration of component (A), the higher should be the concentration of component (C.sub.P) within the stated ranges when dome staining resistance is important, because component (C.sub.P) appears to act synergistically with component (A) to promote dome staining resistance. Higher concentrations of component (B) within the stated ranges are preferred when the concentration of components (D) and/or (E) is relatively high.
Under some conditions of operation, it is preferred that the compositions according to this invention that include amine oxides and/or quaternary ammonium salts do not contain certain materials that are useful for mobility enhancement, even in other embodiments of this invention, and also do not contain certain other materials with various disadvantageous properties. Specifically, independently for each possible component listed below, with increasing preference in the order given, amine oxide and/or quaternary ammonium salt based compositions according to this invention for use in Stage 4 as defined above, either as such or after dilution with water, preferably contain no more than 5, 1.0, 0.2, 0.05, 0.01, 0.003, 0.001, or 0.0005% by weight of any of the following materials [other than those specified as necessary or optional components (A)-(G) above]: (a) surfactants such as (a.1 ) organic phosphate esters, (a.2) alcohols, (a.3) fatty acids including mono-, di-, tri-, and poly-acids and their derivatives (a.4) such as (a.4.1) salts, (a.4.2) hydroxy acids, (a.4.3) amides, (a.4.4) esters, and (a.4.5) ethers; (b) surfactants that are alkoxylated but are otherwise as described in part (a); (c) alkoxylated castor oil triglycerides; (d) sulfate and sulfonate derivatives of natural and synthetically derived alcohols, acids, and/or natural products; (e) amino acids; (f) water-soluble homopolymers and/or heteropolymers of ethylene oxide, propylene oxide, butylene oxide, acrylic acid and its derivatives, maleic acid and its derivatives, and/or vinyl alcohol; and (g) salts of organic acids containing a total of at least two carboxyl and hydroxyl groups.
Preferred water-soluble polymers include homopolymers and heteropolymers of ethylene oxide, propylene oxide, butylene oxide, acrylic acid and its derivatives, maleic acid and its derivatives, vinyl phenol and its derivatives, and vinyl alcohol. Specific examples include Carbowax.TM. 200, Carbowax.TM. 600, Carbowax.TM. 900, Carbowax.TM. 1450, Carbowax.TM. 3350, Carbowax.TM. 8000, and Compound 20M.TM., all available from Union Carbide Corp.; Pluronic.TM. L61, Pluronic.TM. L81, Pluronic.TM. 31R1, Pluronic.TM. 25R2, Tetronic.TM. 304, Tetronic.TM. 701, Tetronic.TM. 908, Tetronic.TM. 90R4, and Tetronic.TM. 150R1, all available from BASF Wyandotte Corp.; Acusol.TM. 410N sodium salt of polyacrylic acid, Acusol.TM. 445 polyacrylic acid, Acusol.TM. 460ND sodium salt of maleic acid/olefin copolymer, and Acusol.TM. 479N sodium salt of acrylic acid/maleic acid copolymer, all available from Rohm & Haas Company; and N-methylglucamine adducts of polyvinylphenol and N-methylethanolamine adducts of polyvinylphenol.
Additional improvements are achieved by combining in the process of this invention the step of additionally contacting the exterior of an aluminum can with an inorganic material selected from metallic or ionic zirconium, titanium, cerium, aluminum, iron, vanadium, tantalum, niobium, molybdenum, tungsten, hafnium or tin to produce a film combining one or more of these metals with one or more of the above-described organic materials. A thin film is produced having a coefficient of static friction that is not more than 1.5 and is preferably less than the coefficient without such film, thereby improving can mobility in high speed conveying without interfering with subsequent lacquering, other painting, printing, or other similar decorating of the containers.
The technique of incorporating such inorganic materials is described, in particular detail with reference to zirconium containing materials, in U.S. Pat. Nos. 5,030,323 of Jul. 9, 1991 and 5,064,500 of Nov. 12, 1991, the entire disclosures of which, to the extent not inconsistent with any explicit statement herein, are hereby incorporated herein by reference. The substitution of other metallic materials for those taught explicitly in one of these patents is within the scope of those skilled in the art.
In a further preferred embodiment of the process of the present invention, in order to provide improved water solubility, especially for the non-ethoxylated organic materials described herein, and to produce a suitable film on the can surface having a coefficient of static friction not more than 1.5 after drying, one employs a mixture of one or more surfactants, preferably alkoxylated and most preferably ethoxylated, along with such non-ethoxylated organic material to contact the cleaned can surface prior to final drying and conveying. Preferred surfactants include ethoxylated and non-ethoxylated sulfated or sulfonated fatty alcohols, such as lauryl and coco alcohols. Suitable are a wide class of anionic, non-ionic, cationic, or amphoteric surfactants. Alkyl polyglycosides such as C.sub.8 -C.sub.18 alkyl polyglycosides having average degrees of polymerization between 1.2 and 2.0 are also suitable. Other classes of surfactants suitable in combination are ethoxylated nonyl and octyl phenols containing from 1.5 to 100 moles of ethylene oxide, preferably a nonylphenol condensed with from 6 to 50 moles of ethylene oxide such as Igepal.TM. CO-887 available from Rhone-Poulenc; alkyl/aryl polyethers, for example, Triton.TM. DF-16; and phosphate esters of which Triton.TM. H-66 and Triton.TM. QS-44 are examples, all of the Triton.TM. products being available from Union Carbide Corp., and Ethox.TM. 2684 and Ethfac.TM. 136, both available from Ethox Chemicals Inc., are representative examples; polyethoxylated and/or polypropoxylated derivatives of linear and branched alcohols and derivatives thereof, as for example Trycol.TM. 6720 (Henkel Corp.), Surfonic.TM. LF-17 (Texaco) and Antarox.TM. LF-330 (Rhone-Poulenc); sulfonated derivatives of linear or branched aliphatic alcohols, for example, Neodol.TM. 25-3S (Shell Chemical Co.); sulfonated aryl derivatives, for example, Dyasulf.TM. 9268-A, Dyasulf.TM. C-70, Lomar.TM. D (all available from Henkel Corp.) and Dowfax.TM. 2A1 (available from Dow Chemical Co.); and ethylene oxide and propylene oxide copolymers, for example, Pluronic.TM. L-61, Pluronic.TM. 81, Pluronic.TM. 31R1, Tetronic.TM. 701, Tetronic.TM. 90R4 and Tetronic.TM. 150R1, all available from BASF Corp.
Further, the lubricant and surface conditioner for aluminum cans in accordance with this invention may comprise a phosphate acid ester or preferably an ethoxylated alkyl alcohol phosphate ester. Such phosphate esters are commercially available under the tradename Rhodafac.TM. PE 510 from Rhone-Poulenc Corporation, Wayne, N.J., and as Ethfac.TM. 136 and Ethfac.TM. 161 from Ethox Chemicals, Inc., Greenville, S.C. In general, the organic phosphate esters may comprise alkyl and aryl phosphate esters with and without ethoxylation.
The lubricant and surface conditioner for aluminum cans may be applied to the cans during their wash cycle, during one of their treatment cycles such as cleaning or conversion coating, during one of their water rinse cycles, or more preferably (unless the lubricant and surface conditioner includes a metal cation as described above), during their final water rinse cycle. In addition, the lubricant and surface conditioner may be applied to the cans after their final water rinse cycle, i.e., prior to oven drying, or after oven drying, by fine mist application from water or another volatile non-inflammable solvent solution. It has been found that the lubricant and surface conditioner is capable of depositing on the aluminum surface of the cans to provide them with the desired characteristics. The lubricant and surface conditioner may be applied by spraying and reacts with the aluminum surface through chemisorption or physiosorption to provide it with the desired film.
The method of contact and the time of contact between the aqueous treating compositions and the metal substrates to be treated and the temperature of the compositions during treatment are generally not critical features of the invention; they may be taken from the known state of the art. However, for large scale operations, power spraying is the preferred method of contact, and times of contact in stage 4 in the range from 5 to 60 seconds ("sec"), or more preferably from 10 to 30 sec, and a temperature of 20.degree. to 60.degree. C., or more preferably 30.degree. to 48.degree. C., are generally used.
Generally, in the cleaning process of the cans, after the cans have been washed, they are typically exposed to an acidic water rinse. In accordance with this invention, the cans may thereafter be treated with a lubricant and surface conditioner comprising an anionic surfactant such as a phosphate acid ester. The pH of the treatment composition is important and generally should be acidic, that is between about 1 and about 6.5, preferably between about 2.5 and about 5. If the cans are not treated with the lubricant and surface conditioner of this invention next after the acidic water rinse, the cans are often exposed to a tap water rinse and then to a deionized water rinse. In such event, the deionized water rinse solution is prepared to contain the lubricant and surface conditioner of this invention, which may comprise a nonionic surfactant selected from the aforementioned polyoxyethylated alcohols or polyoxyethylated fatty acids, or any of the other suitable materials as described above. After such treatment, the cans may be passed to an oven for drying prior to further processing.
The amount of lubricant and surface conditioner remaining on the treated surface after drying should be sufficient to result in a COF value not more than 1.5, or with increasing preference in the order given, to a value of not more than 1.2, 1.0, 0.80, 0.72, 0.66, 0.60, 0.55, or 0.50. Generally speaking, such amount should be on the order of from 3 mg/m.sup.2 to 60 mg/m.sup.2 of lubricant and surface conditioner on the outside surface of the cans. For reasons of economy, it is generally preferred that the aqueous lubricant and surface conditioner forming composition contain, with increasing preference in the order given, not more than 2.0, 1.0, 0.8, 0.6, 0.4, 0.30, or 0.20 grams per liter (often abbreviated hereinafter as "g/L") of the necessary organic material(s) to form the lubricant and surface conditioner film on the treated can surface after drying.
EMBODIMENTS OF THE INVENTION WITH DESIRABLE SPECIAL CHARACTERISTICS
Resistance to Increasing Friction by Overheating of Treated Containers
In accordance with a particular preferred embodiment of this invention, it has been found that the coefficient of friction of a surface treated, after primary cleaning of the surface, with a lubricant and surface conditioner is less easily damaged by heating when the lubricant and surface conditioner composition includes at least one of the following organic materials: alkoxylated or non-alkoxylated castor oil triglycerides and hydrogenated castor oil derivatives; alkoxylated and non-alkoxylated amine salts of a fatty acid including mono-, di-, tri-, and poly-acids; alkoxylated and non-alkoxylated amino fatty acids; alkoxylated and non-alkoxylated fatty amine N-oxides, alkoxylated and nonoalkoxylated quaternary ammonium salts, alkyl esters of 2-substituted alkoxylated fatty alkyloxy acetic acids (briefly denoted hereinafter as "oxa-acid esters") as described more fully in U.S. application Ser. No. 843,135 filed Feb. 28, 1992, the disclosure of which is hereby incorporated herein by reference, and water-soluble alkoxylated and non-alkoxylated polymers. Furthermore, if the lubricant and surface conditioner is not applied to the surface from the last aqueous composition with which the surface is contacted before the last drying of the surface before automatic conveying, the composition including the organic materials preferably also includes a metallic element selected from the group consisting of zirconium, titanium, cerium, aluminum, iron, tin, vanadium, tantalum, niobium, molybdenum, tungsten, and hafnium in metallic or ionic form, and the film formed on the surface as part of the lubricant and surface conditioner in dried form should include some of this metallic element along with organic material.
Friction Reducing Treatment as Part of Primary Cleaning
When the last contact of the treated metal surfaces with materials suitable for forming a lubricant and surface conditioner layer thereon is to occur in Stage 2 as described above, many of the preferences given above need to be modified somewhat, as discussed further below.
One particularly marked deviation from most current commercial practice is that if mobility enhancing materials are to be added to a Stage 2 cleaner, the cleaner should be alkaline. More specifically, the pH of the composition preferably is, with increasing preference in the order given, at least 11.0, 11.2, 11.4, 11.5, 11.6, 11.7, 11.8, 11.9, or 12.0 and independently preferably is, with increasing preference in the order given, not more than 12.5, 12.4, 12.3, 12.2, or 12.1. In general, higher pH values within this range produce better interior brightness and external appearance, but lower pH values within this range produce treated surfaces with lower COF values and therefore better mobility. Because the mobility is adequate for most purposes even at the higher end of the range, a pH value of 12.0 to 12.1 is generally most preferred.
The contact time may be varied over wide limits, but generally preferably is, with increasing preference in the order given, at least 3, 8, 15, 25, 38, 46, 54, or 57 sec and independently preferably is, with increasing preference in the order given, not more than 300, 150, 100, 83, 75, 68, or 63 sec. The temperature during contact similarly may be varied within wide limits, but generally preferably is, with increasing preference in the order given, at least 20.degree., 25.degree., 30.degree., 34.degree., 37.degree., 40.degree., 42.degree., or 44.degree. C. and independently preferably is, with increasing preference in the order given, not more than 95.degree., 85.degree., 75.degree., 66.degree., 61.degree., 57.degree., or 54.degree. C. The contact method is also not critical, but spraying is generally preferred.
In addition to an alkalinity agent to achieve the pH levels noted above, an alkaline cleaning composition in which a mobility enhancing lubricant and surface conditioner film forming material is to be included preferably contains (i) a complexing agent component present in an amount effective to complex at least some of the metal ions in the operating bath which tend to form bath insoluble precipitates and (ii) one or a combination of selected surfactants in an amount sufficient to (ii.1) remove the organic soils present on the substrate being cleaned, (ii.2) prevent a buildup of such organic soils in the cleaning solution, (ii.3) prevent redeposition of organic soils on cleaned cans, and/or (ii.4) inhibit white etch staining. The composition may optionally contain a foam-suppressant agent of any of the types conventionally employed in otherwise similar alkaline cleaning solutions, depending on the types of surfactants used in the cleaning composition and the manner in which the aqueous cleaning composition is applied to the substrate, to minimize undesirable foaming thereof.
A make-up or replenishment of the cleaning composition can conveniently be effected by employing a dry-powdered concentrate of the active constituents or, alternatively, a concentrated aqueous solution or slurry, facilitating addition and admixture with the operating cleaning composition during use.
The alkalinity agent may comprise any one or a combination of bath soluble and compatible compounds including alkali or alkaline earth metal borates, carbonates, hydroxides, or phosphates, as well as mixtures thereof; alkali metal hydroxides and alkali metal carbonates constitute the preferred materials, with sodium hydroxide being particularly preferred. The alkalinity agent preferably is prepared and maintained in the operating bath at a concentration effective to remove substantially all of the aluminum fines on the container surfaces while at the same time not unduly etching the aluminum surface, so as to provide a clean, bright, reflective appearance; such effectiveness is normally achieved when the pH values of the operating bath is maintained within the ranges given above. Normally, in order to achieve a pH value within the desired range, the alkalinity agent or combinations thereof are employed at a concentration of from 0.05 up to 10 g/L, with concentrations of 0.4 to 3.5 g/L usually being preferred because they will normally result in a pH value within one of the more preferred ranges.
The complexing agent may comprise any one or a combination of bath soluble and compatible compounds which are effective to complex at least some of the metal ions present in the operating bath to avoid the formation of deleterious precipitates. Included among such complexing agents suitable for use in the alkaline cleaner of the present invention are gluconic acid, citric acid, glucoheptanoic acid, sodium tripolyphosphate, ethylene diamine tetraacetic acid (.music-flat.EDTA"), tartaric acid or the like, as well as the bath soluble and compatible salts thereof and mixtures thereof. Preferably, the complexing agents are selected from molecules conforming to one of the general formulas Q--(CHOH).sub.a --Q' and MOOC--[CH.sub.2 C(OH)(COOM')].sub.b --COOM"', where each of Q and Q', which may be the same or different, represents either CH2OH or COOM; each of M, M' and M'", which may be the same or different, represents hydrogen or an alkali metal cation; a is an integer with a value of at least 2 and preferably not more than 6, more preferably not more than 5; and b is an integer with a value of at least 1, preferably not more than 3. Generally, the concentration of the complexing agent in the operating bath preferably is, with increasing preference in the order given, not less than 0.2, 0.4, 0.7, 1.0, 1.3, 1.6, 1.9, 2.1, 2.3, 2.5, 2.7, 2.9, 3.1, 3.3, 3.4, 3.5, 3.6, 3.7, or 3.8 millimoles per liter ("mM") and independently preferably is, with increasing preference in the order given, not more than 50, 35, 20, 15, 10, 8, 7, 6.5, 6.0, 5.7, 5.4, 5.2, 5.0, or 4.9 mM.
A third preferred ingredient of the alkaline cleaning solution is a cleaning surfactant component which has a Hydrophile-Lipophile Balance ("HLB"), i.e., the balance of the size and strength of the hydrophilic (water-loving or polar) and the lipophilic (oil-loving or non-polar) groups of the molecule, in the range from 12 to 15. (For information regarding the determination of the HLB number of surfactants and emulsifying agents, reference is made to Chapter 7, pages 18 and 19 of a publication titled The Atlas HLB System, Third Edition, 1963, by Atlas Chemical Industries, Inc.) Generally, an HLB number of at least 12 is preferred to achieve an efficient removal of lubricants and organic soils of the types customarily employed in the drawing and ironing of aluminum containers, at relatively low surfactant concentrations, while inhibiting white etch stain. If the surfactant has an HLB number in excess of 15, increased amounts of surfactant are generally necessary to achieve satisfactory cleaning of the container bodies and to avoid undesirable buildup, in the aqueous alkaline cleaning composition, of the concentration of organic soils, which tend to redeposit on the container surfaces. Even more preferably, the HLB value is at least 13.
Commercial surfactants which have been found particularly satisfactory for cleaning use in accordance with the present invention include Tergitol.TM. 15-S-9, reportedly comprising an ethoxylated secondary alcohol (with an HLB value of about 13.5), available from Union Carbide Corporation; Neodol.TM. 91-8, reportedly comprising an ethoxylated linear alcohol (with an HLB value of about 14.1 ), commercially available from Shell Chemical Company; [Igepal.TM. CO-630, reportedly comprising an ethoxylated alkyl nonylphenol (with an HLB value of about 13.0), commercially available from Rhone-Poulenc; and Triton.TM. N-101, reportedly having the same general chemical description as noted for Igepal.TM. CO-630, but with a slightly lower degree of ethoxylation and an HLB value of 13.1, and commercially available from Union Carbide Corp.
Additional cleaning surfactants suitable for use in the practice of the present invention include, for example, those having hydrophobic groups comprising alkyl phenols, linear alcohols, branched-chain alcohols, secondary alcohols, propylene oxide/propylene glycol condensates, or the like and hydrophilic groups such as ethylene oxide, ethylene oxide/ethylene glycol condensates, or the like which may further contain capping groups such as propylene oxide, chloride, benzyl chloride, amines, or the like.
Alkoxylated cleaning surfactants of the foregoing types can be represented by the general structural formula: R(OR').sub.n OH, wherein R is a monovalent hydrocarbon moiety containing 6 to 30 carbon atoms, R' is an alkylene or propylene group, and n is an integer with a value from 5 to 100. The active hydrogen at the end of this general structural formula can be substituted by employing conventional capping groups in accordance with known techniques.
Preferably, the cleaning surfactant component is employed at a concentration that is, with increasing preference in the order given, at least 0.01, 0.05, 0.10, 0.20, 0.30, 0.35, 0.39, 0.42, 0.44, 0.46, 0.47, 0.48, 0.48, or 0.50 g/L and independently preferably is not more than 50, 25, 15, 10, 5, 4, 3, 2.5, 2.0, 1.7, 1.5, 1.4, 1.3, 1.2, 1.1, or 1.0 g/L.
The lubricant and surface conditioner forming component, alternatively called "mobility enhancer", in an alkaline primary cleaning composition preferably is chosen from the group consisting of quaternary ammonium salts and ethoxylated phosphate esters, both as described generally above. Quaternary ammonium salts are more preferred when minimization of water-breaks is desired, as it generally is. Particularly preferred lubricant and surface conditioner forming quaternary ammonium salts are those having (i) one long alkyl or alkenyl moiety, preferably a straight chain moiety with from 10 to 22, more preferably from 12 to 18 carbon atoms, attached to one quaternary nitrogen atom in each molecule; (ii) at least two, more preferably at least three, hydroxyalkyl moieties with from 2 to 4, most preferably two, carbon atoms in each such hydroxyalkyl moiety also attached to each quaternary nitrogen atom; and (iii) alkyl or allkenyl moieties, optionally aryl substituted or including a quaternary ammonium group or both, with from 1 to 8 carbon atoms exclusive of those in any other substituents of any quaternary ammonium group present in the alkyl or alkenyl group; each of these chemical characteristics (i)-(iii) as noted immediately above is preferred individually as well as jointly.
In order to form within a reasonable contact time an amount of lubricant and surface conditioner layer that adequately reduces surface friction, it is preferred that an alkaline cleaner also containing a mobility enhancer should contain, with increasing preference in the order given, at least 0.05, 0.12, 0.25, 0.46, 0.60, 0.75, 0.87, 1.00, 1.12, or 1.22 g/L of the mobility enhancer. Independently, in order to avoid excessive cost, it is preferred, with increasing preference in the order given, that the concentration of mobility enhancer in a working alkaline cleaner should not exceed 12, 5, 3.5, 2.7, 2.3, 2.1, 1.9, 1.82, 1.74, 1.67, 1.60, or 1.53 g/L. (In a concentrate composition, intended for dilution with water before actual use in cleaning, optimal concentrations would of course be higher than these.)
Depending upon the particular type of surfactant or surfactants used, the manner of application of the cleaning solution to the aluminum containers and the concentration and processing parameters, it is further contemplated that an antifoaming agent can also be incorporated in the cleaning composition to avoid objectionable foaming. Any one of a variety of commercially available antifoaming agents can be employed for this purpose; agents based on micro-crystalline wax have been found particularly satisfactory.
It is also known that it is desirable to subsequently rinse an alkaline cleaned surface with an aqueous based neutral or acidulated rinse solution at a controlled pH to remove residual cleaning solution therefrom. Brown oxide discoloration of alkaline cleaned aluminum containers that might otherwise occur during or shortly after water rinsing thereof following the primary alkaline cleaning stage can be substantially eliminated by employing a water rinse in which the pH is maintained at substantially neutral or on the acidic side. Because of a carry-over or drag-out of the aqueous alkaline cleaning solution into the following rinse stage, such a rinse generally becomes progressively more alkaline, in the absence of preventive measures. In order to avoid any buildup in alkalinity of the subsequent rinse stages, it has been found advantageous to effect an overflow of the rinse and/or a neutralization of any alkaline buildup by the addition of acid, so as to maintain the pH of the rinse solution at a level preferably less than about pH 7.5 and more preferably at about pH 7 or below. By maintaining the subsequent water rinse solutions at a near-neutral or acidic pH, the formation of brown stains on the aluminum container bodies is substantially eliminated, even when there are line stoppages in the rinsing stage.
Under many operating conditions, it is desirable to avoid the use of fluorine in any chemical form in order to avoid environmental pollution at minimum cost. The alkaline cleaning processes as described above are well suited to this goal, and it is accordingly often preferred that any aqueous composition used in such a process, independently for each composition as well as jointly for all of them, should contain, with increasing preference in the order given, not more than 1.0, 0.5, 0.3, 0.2, 0.15, 0.10, 0.07, 0.04, 0.02, 0.01, 0.005, or 0.001 g/L of fluorine in any chemical form.
For a fuller appreciation of the invention, reference may be made to the following examples, which are intended to be merely descriptive, illustrative, and not limiting as to the scope of the invention, except to the extent that their limitations may be incorporated into the appended claims.
Example Group 1
This example illustrates the amount of aluminum can lubricant and surface conditioner necessary to improve the mobility of the cans through the tracks and printing stations of an industrial can manufacturing facility, and also shows that the lubricant and surface conditioner does not have an adverse effect on the adhesion of labels printed on the outside surface as well as of lacquers sprayed on the inside surface of the cans.
Uncleaned aluminum cans obtained from an industrial can manufacturer were washed clean with an alkaline cleaner available from PA, employing that company's Ridoline.TM. 3060/306 process. The cans were washed in a carousel can washer (hereinafter often abbreviated as "CCW") processing 14 cans at a time. The cans were treated with different amounts of lubricant and surface conditioner in the final rinse stage of the CCW and then dried in an oven. The lubricant and surface conditioner comprised about a 10% active concentrate of polyoxyethylated isostearate, an ethoxylated nonionic surfactant, available under the tradename Ethox.TM. MI-14 from Ethox Chemicals, Inc., Greenville, S.C. The treated cans were returned to the can manufacturer for line speed and printing quality evaluations. The primed cans were divided into two groups, each consisting of 4 to 6 cans. All were subjected for 20 minutes to one of the following adhesion test solutions:
Test Solution A: 1% Joy.TM. (a commercial liquid dishwashing detergent, Procter and Gamble Co.) solution in 3:1 deionized water:tap water at a temperature of 82.degree. C.
Test Solution B: 1% Joy.TM. detergent solution in deionized water at a temperature of 100.degree. C.
After removing the printed cans from the adhesion test solution, each can was cross-hatched using a sharp metal object to expose lines of aluminum which showed through the paint or lacquer, and tested for paint adhesion. This test included applying Scotch.TM. transparent tape No. 610 firmly over the cross-hatched area and then drawing the tape back against itself with a rapid pulling motion such that the tape was pulled away from the cross-hatched area. The results of the test were rated as follows: 10, perfect, when the tape did not peel any paint from the surface; 8, acceptable; and 0. total failure. The cans were visually examined for any print or lacquer pick-off signs.
In addition, the cans were evaluated for their coefficient of static friction using a laboratory static friction tester. This device measures the static friction associated with the surface characteristics of aluminum cans. This is done by using a ramp which is raised through an arc of 90.degree. by using a constant speed motor, a spool and a cable attached to the free swinging end of the ramp. A cradle attached to the bottom of the ramp is used to hold 2 cans in horizontal position approximately 1.3 centimeters apart with the domes facing the fixed end of the ramp. A third can is laid upon the 2 cans with the dome facing the free swinging end of the ramp, and the edges of all 3 cans are aligned so that they are even with each other.
As the ramp begins to move through its are, a timer is automatically actuated. When the ramp reaches the angle at which the third can slides freely from the 2 lower cans, a photoelectric switch shuts off the timer. It is this time, recorded in seconds, which is commonly referred to as "slip time". The coefficient of static friction is equal to the tangent of the angle swept by the ramp at the time the can begins to move. This angle in degrees is equal to [4.84+(2.79.multidot.t)], where t is the slip time. In some cases the tested cans were subjected to an additional bake out at 210.degree. C. for 5 minutes and the COF redetermined; this result is denoted hereinafter as "COF-2".
The average values for the adhesion test and coefficient of static friction evaluation results are summarized in Table 2. In brief, it was found that the lubricant and surface conditioner concentrate as applied to the cleaned aluminum cans provided improved mobility to the cans even at very low use concentrations, and it had no adverse effect on either adhesion of label print or internal lacquer tested even at 20 to 100 times the use concentration required to reduce the coefficient of static friction of the cans.
TABLE 2______________________________________Lubricant andSurface Con- Adhesion Evaluation ditioner Con- TestTest centrate Solu- Coefficient ofNo. (%/vol.) tion OSW ISW ID Static Friction______________________________________1 Control (no -- -- -- -- 1.42 treatment)2 0.1 B 10 10 10 0.943 0.25 A 10 10 10 --4 0.5 B 9.5* 10 10 0.805 0.75 A 10 10 10 0.636 1.0 B 10 10 10 0.647 2.0 A 10 10 10 0.568 5.0 B 10 10 10 0.559 10.0 A 9.8* 10 10 0.56______________________________________ Notes for Table 2 *Little pickoff was visually noticed on the outside walls, mainly at the contact marks. "OSW" stands for outside sidewall, "ISW" stands for inside sidewall, and "ID" stands for inside dome.
Example Group 2
These examples illustrate the use of the aluminum can lubricant and surface conditioner of Example Group 1 in an industrial can manufacturing facility when passing cans through a printing station at the rate of 1260 cans per minute.
Aluminum can production was washed with an acidic cleaner (Ridoline.TM. 125 CO, available from PA), and then treated with a non-chromate conversion coating (Alodine.TM. 404, also available from the ParkerAmchem Division, Henkel Corporation, Madison Heights, Mich.). The aluminum can production was then tested for "slip" and the exterior of the cans were found to have a static coefficient of friction of about 1.63. During processing of these cans through a printer station, the cans could be run through the printer station at the rate of 1150 to 1200 cans per minute without excessive "trips", i.e., improperly loaded can events. In such case, the cans are not properly loaded on the mandrel where they are printed. Each "trip" causes a loss of cans which have to be discarded because they are not acceptable for final stage processing.
About 1 ml/liter of aluminum can lubricant and surface conditioner was added to the deionized rinse water system of the can washer, which provided a reduction of the static coefficient of friction on the exterior of the cans to a value of 1.46 or a reduction of about 11 percent from their original value. After passing the cans through the printer, it was found that the adhesion of both the interior and exterior coatings were unaffected by the lubricant and surface conditioner. In addition, the printer speed could be increased to its mechanical limit of 1250 to 1260 cans per minute without new problems.
In similar fashion, by increasing the concentration of the aluminum can lubricant and the surface conditioner to the deionized rinse water system, it was possible to reduce the coefficient of static friction of the cans by 20 percent without adversely affecting the adhesion of the interior and exterior coatings of the cans. Further, it was possible to maintain the printer speed continuously at 1250 cans per minute for a 24-hour test period.
Example and Comparison Example Group 3
These examples illustrate the use of other materials as the basic component for the aluminum can lubricant and surface conditioner.
Aluminum cans were cleaned with an alkaline cleaner solution having a pH of about 12 at about 41.degree. C. for about 35 seconds. The cans were rinsed, and then treated with three different lubricant and surface conditioners comprising various phosphate ester solutions. Phosphate ester solution 1 comprised a phosphate acid ester (available under the tradename Rhodafac.TM. PE 510 from Rhone-Poulenc, Wayne, N.J.) at a concentration of 0.5 g/L. Phosphate ester solution 2 comprised an ethoxylated alkyl alcohol phosphate ester (available under the tradename Ethfac.TM. 161 from Ethox Chemicals, Inc., Greenville, S.C.) at a concentration of 0.5 g/L. Phosphate ester solution 3 comprised an ethoxylated alkyl alcohol phosphate ester (available under the tradename Ethfac.TM. 136 from Ethox Chemicals, Inc., Greenville, S.C.) at a concentration of 1.5 g/L.
The mobility of the cans in terms of coefficient of static friction was evaluated and found to be as follows in Table 3:
TABLE 3______________________________________ Coefficient of staticPhosphate ester solution pH friction______________________________________1 3.6 0.472 3.3 0.633 2.6 0.77None -- 1.63______________________________________
The aforementioned phosphate ester solutions all provided an acceptable mobility to aluminum cans, but the cans were completely covered with "water-break". It is desired that the cans be free of water-breaks, i.e., have a thin, continuous film of water thereon, because otherwise they contain large water droplets, and the water film is non-uniform and discontinuous. To determine whether such is detrimental to printing of the cans, they were evaluated for adhesion. That is, the decorated cans were cut open and boiled in a 1% liquid dishwashing detergent solution (Joy.TM.) comprising 3:1 deionized water:tap water for ten minutes. The cans were then rinsed in deionized water and dried. As in Example Group 1, eight cross-hatched scribe lines were cut into the coating of the cans on the inside and outside sidewalls and the inside dome. The scribe lines were taped over, and then the tape was snapped off. The cans were rated for adhesion values. The average value results are summarized in Table 4, in which the acronyms have the same meaning as in Table 2.
TABLE 4______________________________________Phosphate Ester Adhesion Rating on:Solution Used OSW ISW ID______________________________________control 10 10 101 9.8 6.8 1.02 9.8 10 103 10 10 10______________________________________
For the control, it was observed that there was no pick-off (loss of coating adhesion) on either the outside sidewall, the inside sidewall or the inside dome of the cans. For phosphate ester solution 1, it was observed that there was almost no pick-off on the outside sidewall, substantial pick-off on the inside sidewall, and complete failure on the inside dome of the cans. For phosphate ester solution 2, it was observed that there was almost no pick-off on the outside sidewall, and no pick-off on the inside sidewall and no pick-off on the inside dome of the cans. For phosphate ester solution 3, it was observed that there was no pick-off on the outside sidewall, the inside sidewall, or the inside dome of the cans.
Example Group 4
This example illustrates the effect of the lubricant and surface conditioner of this invention on the water draining characteristics of aluminum cans treated therewith.
Aluminum cans were cleaned with acidic cleaner (Ridoline.TM. 125 CO followed by Alodine.TM. 404 treatment or Ridoline.TM. 125 CO only) or with an alkaline cleaner solution (Ridoline.TM. 3060/306 process), all the products being available from the Parker Amchem Division, Henkel Corporation, Madison Heights, Mich., and then rinsed with deionized water containing about 0.3% by weight of the lubricant and surface conditioner of this invention. After allowing the thus-rinsed cans to drain for up to 30 seconds, the amount of water remaining on each can was determined. The same test was conducted without the use of the lubricant and surface conditioner. The results are summarized in Table 5. It was found that the presence of the lubricant and surface conditioner caused the water to drain more uniformly from the cans, and that the cans remain "water-break" free for a longer time.
TABLE 5______________________________________Drain Time Grams per Can of Water Remaining Using:in Seconds DI Water DI Water + 0.3% Conditioner______________________________________ 6 2.4-3.0 nd12 2.1-3.5 2.818 2.2-3.5 2.330 1.8-3.4 2.3______________________________________
Example Group 5
This example illustrates the effect of the oven dryoff temperature on the sidewall strength of aluminum cans. This test is a quality control compression test which determines the column strength of the cans by measuring the pressure at which they buckle. The results are summarized in Table 6.
It can be seen from. Table 6 that at an oven drying temperature of 193.degree. C., a 2 pounds per square inch ("psi") increase, compared to the value obtained at 227.degree. C. oven temperature, was obtained in the column strength test.
TABLE 6______________________________________Oven Temperature (.degree.C.) Column Strength (PSI)______________________________________227 86.25204 87.75193 88.25182 89.25______________________________________
The higher column strength test results are preferred and often required because the thin walls of the finished cans must withstand the pressure exerted from within after they are filled with a carbonated solution. Otherwise, cans having weak sidewalls will swell and deform or may easily rupture or even explode. It was found that the faster water film drainage resulting from the presence therein of the lubricant and surface conditioner composition of this invention makes it possible to lower the temperature of the drying ovens and in turn obtain higher column strength results. More specifically, in order to obtain adequate drying of the rinsed cans, the cans are allowed to drain briefly before entry into the drying ovens. The time that the cans reside in the drying ovens is typically between 2 and 3 minutes, dependent to some extent on the line speed, oven length, and oven temperature. In order to obtain adequate drying of the cans in this time-frame, the oven temperature is typically about 227.degree. C. However, in a series of tests wherein the rinse water contained about 0.3% by weight of organic material to form a lubricant and surface conditioner of this invention, it was found that satisfactory drying of the cans could be obtained wherein the oven temperature was lowered to 204.degree. C., and then to 188.degree. C., and dry cans were still obtained.
Examples Group 6
Uncleaned aluminum cans from an industrial can manufacturer are washed clean in examples Type A with alkaline cleaner available from ParkerAmchem Division, Henkel Corporation, Madison Heights, Mich., employing the Ridoline.TM. 3060/306 process and in Examples Type B with an acidic cleaner, Ridoline.TM. 125 CO from the same company. Following initial rinsing and before final drying, the cleaned cans are treated with a lubricant and surface conditioner comprised of about a 1% by weight active organic (I) in deionized water as specified in Table 7 below. In a separate set of examples, following initial rinsing and before final drying, the cleaned cans are treated with a reactive lubricant and surface conditioner comprised of about a 1% active organic (I) in aleionized water plus about 2 g/L (0.2 wt %) of the inorganic (II) as specified in Table 7 below. In yet another set of examples, following initial rinsing and before final drying, the cleaned cans are treated with a lubricant and surface conditioner comprised of about 1% active organic (I) in aleionized water plus about 0.5% by weight of surfactant (III) specified in Table 7 below. In a further set of examples, following initial rinsing and before final drying, the cleaned cans are treated with a reactive lubricant and surface conditioner forming component, in deionized water, comprised of about 1% of active organic (I), about 0.2% of inorganic (II), and about 0.5% of surfactant (III) as specified in Table 7 below. In all cases in this group of examples, the COF produced on the surface is less than 1.5.
TABLE 7__________________________________________________________________________Example Active Organic (I)Type Trade Name Chemical Description Inorganic (II) Surfactant (III) pH__________________________________________________________________________A Emery 657 Caprylic acid Al.sub.2 (SO.sub.4).sub.3 IGEPAL CO-887 2.2B Emery 659 Capric acid H.sub.2 ZrF.sub.6 TRITON X-101 2.2A Emery 651 Lauric acid FeF.sub.3 NEODOL 25-5-3 2.3B Emery 655 Myristic acid SnCl.sub.4 TERGITOL TMN-6 2.3A Emersol 143 Palmitic acid 91% Ce(NO.sub.3).sub.4 TRITON DF-16 2.6B Emersol 153 NF Stearic acid 92% H.sub.2 TiF.sub.6 TRYCOL 6720 2.6A Emersol 871 Isostearic acid H.sub.2 HfF.sub.6 ANTAROX LF-330 2.6B Emersol 6313 NF Oleic acid 75% (NH.sub.4).sub.2 ZrF.sub.6 TRITON H-55 2.6A Empol 1014 Dimer acid 95% Fe.sub.2 (SO.sub.4).sub.3 TRITON H-66 2.6B Emery 1110 Azelaic acid Al(NO.sub.3).sub.3 TRITON QS-44 2.6B Ethox MI5 Ethoxylated isostearic acid TiCl.sub.4 TRYCOL 6720 3.0A Emulphor VN 430 Polyoxyethylated oleic acid CeI.sub.3 SURFONIC LF-17 3.0B Ethox MO5 Polyoxyethylated oleic acid FeF.sub.3 LOMAR D 3.0A Monamide 150 LW Lauric alkanolamide FeCl.sub.3 DOWFAX 2A1 2.0B Monamide 150 MW Myristic alkanolamide FeBr.sub.3 DYASULF 9268-A 3.0A Monamide 150 IS Isostearic alkanolamide H.sub.2 ZrF.sub.6 DYASULF C-70 4.0B Monamide 718 Stearic alkanolamide H.sub.2 TiF.sub.6 IGEPAL CO-887 5.0A Rhodafac BH 650 Aliphatic phosphate ester, Fe(NO.sub.3).sub.3 POLYTERGENT SLF-18 2.0 acid formB Ethox PP16 Aromatic phosphate ester (NH.sub.4).sub.2 ZrF.sub.6 PLURONIC L-61 3.0A Rhodafac BL 750 Aliphatic phosphate ester, TaF.sub.5 TETRONIC 701 6.0 acid formB Rhodafac PE510 Aromatic phosphate ester, NbF.sub.5 PLURONIC 31R1 5.0 acid formA Ethfac 142W Aliphatic phosphate ester H.sub.2 ZrF.sub.6 PLURONIC 150R1 4.0B Rhodafac RA 600 Aliphatic phosphate ester, (NH.sub.4).sub.2 MoO.sub.4 APG 300 6.0 acid formA Armeen Z N-Coco-B-aminobutyric acid H.sub.2 TiF.sub.6 TRITON CF-21 6.0B Hamposyl L Lauroyl sarcosine VF.sub.4 TRITON DF-18 5.0A Hamposyl C Cocoyl sarcosine FeF.sub.3 TRITON GR-7M 4.0B Hamposyl O Oleoyl sarcosine SnCl.sub.4 TRITON H-55 3.0A Hamposyl S Stearyl sarcosine Al.sub.2 (SO.sub.4).sub.3 TRITON X-100 2.0B Acusol 410N Polyacrylic acid, sodium salt, H.sub.2 ZrF.sub.6 TRITON X-120 4.0B Triton GR-5M Dioctylsulfosuccinate Al(NO.sub.3).sub.3 TRYCOL 5882 6.0A Avanel S 70 Sodium alkylether sulfonate VOSO.sub.4 TRYCOL 5887 5.0B Igepon TC-42 Sodium N-coconut and N- VF.sub.5 TRYCOL 5964 4.0 methyl taurateA Igepon TK-32 Sodium N-methyl-N-tall oil VF.sub.3 IGEPAL CO-887 3.0 acid taurateB Neodol 25-3A Sulfonated linear alcohol, (NH.sub.4).sub.2 WO.sub.4 IGEPAL CO-630 3.0 ammonium saltA Aromox C/12 Bis(2-hydroxyethyl) (NH.sub.4).sub.2 ZrF.sub.6 NEODOL 25-3 3.0 cocamine oxideB Aromox DMC Dimethylcocamine oxide FeF.sub.3 NEODOL 25-35 3.0A Ethoquad 0/25 Oleyl [POE(15)] ammonium Fe.sub.2 (SO.sub.4).sub.3 NEODOL 25-9 2.0 chlorideB Ethoquad C/12 Cocomethyl [POE(2)] Al.sub.2 (SO.sub.4).sub.3 NEODOL 91-25 3.0 ammonium chlorideA Ethoquad 18/5 Octadecyl [POE(15)] Sn(SO.sub.4) TRITON QS-15 3.0 ammonium chlorideB Propoquad T/12 Tallowalkylmethyl-bis-(2- Ce.sub.2 (SO.sub.4).sub.3 TRITON DF-12 2.0 hydroxy-2-methylethyl) ammonium methyl sulfateA Ethfac 136 Phosphate ester H.sub.2 ZrF.sub.6 IGEPAL CO-887 2.3B Ethox 2684 Phosphate ester H.sub.2 ZrF.sub.6 IGEPAL CO-887 2.7A Trylox 5922 Ethoxylated hydrogenated H.sub.2 ZrF.sub.6 IGEPAL CO-887 2.3 castor oilB Trylox 5921 Ethoxylated hydrogenated H.sub.2 TiF.sub.6 IGEPAL CO-887 2.7 castor oilA Trylox 5925 Ethoxylated hydrogenated H.sub.2 ZrF.sub.6 TRITON H-66 2.7 castor oil__________________________________________________________________________
Examples and Comparison Examples Group 7
In this group, various candidate materials for forming a lubricant and surface conditioner were tested at lower concentrations than in Group 6.
7.1 General Procedures
Mobility enhancer/rinse aid process solutions were prepared using deionized water with a conductivity less than 5 .mu.siemens; unless otherwise noted, all other solutions were prepared in tap water. Drawn and wall ironed aluminum cans were obtained from commercial factory production.
Most cans were tested on a pilot scale beltwasher, a single track seven stage conveyor belt type washer (hereinafter denoted "BW") at its highest speed of 6.2 feet per minute ("fpm"). Alternatively, the CCW already noted, which processes 14 cans in a sequence of batch steps under microprocessor control, was employed. Both types of washer were capable of simulating the sequences, dwell and blow off characteristics of full scale production washers.
Free Acidity and Fluoride Activities of the cleaner baths were determined as described in the PA Technical Process Bulletin (No. 968) for Ridoline 124C. The cleaned and treated cans were dried in an electric forced air oven as described below. Can mobility was tested as in Group 1.
Foam heights were determined by placing 50 milliliters (hereinafter "mL") of the process solution in a 100 mL stoppered graduated cylinder and shaking vigorously for 10 seconds. The total volume of fluid, liquid plus foam, was determined immediately and after 5 minutes of standing. These "foam heights" will be referred to hereinafter as "IFH" (initial foam height) and "PFH" (persistent foam height) respectively.
The water break characteristics of cans treated with candidate final rinse mobility enhancers ("FRME's) were evaluated by visually rating the amount of waterbreak on each of the four major surfaces of the can: interior dome and sidewall and exterior dome and sidewall. In this rating scheme a value of 2 is assigned to a completely waterbreak free surface, zero to a completely waterbroken surface and intermediate values to waterbreaks in between. Four cans are evaluated in this way and the scores totaled to give a number between 32 and 0, the waterbreak free (WBF) rating number.
7.2 Effect of Cleaner Bath Fluoride Activity On COF and Reflectivity
The CCW and subsequent drying oven were used as follows:
______________________________________Stage 1 tap water, 54.4.degree. C., 30 sec.Stage 2 RIDOLINE .TM. 124C, 15 mL Free Acid, 3.4 g total of surfactant, Fluoride Activity 10 to -20 mV in 10 mV in- crements, 60.degree. C., 60 sec.Stage 3 tap water, 30 sec.Stage 4 deionized water, 90 sec.Stage 5 optional application of 0.4% ME-40 .TM., 20 sec.Stage 6 not usedOven 5 minutes at 210.degree. C.______________________________________
(Note: In this and subsequent descriptions herein of the particular chemical compositions used in various "Stages", the stage number refers only to the order of the mechanical equipment treatment stations used in an equipment train which has six such stations, and does not necessarily imply that the same chemical types of treatments as are listed for the same stage number in Table 1 are used.)
The "fluoride activity" noted for Stage 2 above is defined and can conveniently be measured by means of a fluoride sensitive electrode as described above and in more detail in U.S. Pat. No. 3,431,182.
Effectiveness of soil removal was measured by use of the "brightness tester." This device consisted of a power stabilized high intensity lamp and a fiber optic bundle conveying the light to the can surface. The light reflected from the can impinged on a photocell whose current output was amplified and converted to a digital readout by an International Microtronics Inc. Model 350 amplifier; the number displayed was recorded as the brightness of the surface. The instrument is calibrated with a back silvered plane mirror to a measured reflectivity of 440. Once calibrated, the reflectivities of fourteen cans were measured and averaged. With this device it was possible to measure the overall interior reflectivity and exterior dome reflectivity. Results are shown in FIGS. 1(a)-1(d).
These results indicate that brightness increases monotonically within the range shown with increasing fluoride activity. COF values, in contrast, appear to peak at fluoride activities corresponding to about +10 mv readings and decrease slightly with either increases or decreases from that range. The variation of COF with fluoride activity level in these experiments is actually of relatively little practical importance, compared to the substantial improvement obtained by using a suitable FRME material.
If the results shown in FIGS. 1(a)-1(d) were the only practically important considerations, they would favor the highest fluoride activity levels. For several reasons, however, this has not been found to be true in commercial practice. High fluoride levels are more costly and promote high etching rates that may increase pollution abatement costs or even damage an etched container's ability to contain pressurized contents such as carbonated beverages. Also, in integrated commercial operations where there is a relatively short time between can formation and cleaning, the oily residues from can forming are easier to remove than in the laboratory experiments, where at least a few hours of time normally elapses between forming a set of cans and cleaning them. As a result of these factors, fluoride activity levels corresponding to electrode readings of from +50 to -10 mv have been found to be generally preferred, with electrode readings from +5 to 0 most preferred. As would be expected from the results shown in FIGS. 1(b) and 1(d), higher fluoride activities within these ranges are preferred when high brightness of the cans is required.
7.3 Screening of Diverse Materials For FRME Activity
The CCW was operated according to the following scheme, in which the extended Stage 3 rinse time simulated a production sequence wherein the normal Stage 3, 4, and 5 applications were used as rinses:
______________________________________Stage 1 sulfuric acid, pH 2.0, 30 sec., 54.4.degree. C.Stage 2 RIDOLINE .TM. 124C, 15 mL Free Acid, 3.4 g/L total of surfactant, Fluoride Activity -10 mV, 90 sec., 54.4.degree. C.Stage 3 deionized water, 150 sec. (ca. 17.7 L)Stage 4 as noted in Table 8, 30 sec., 29.4.degree. C. temperatureStage 5 not usedStage 6 not used______________________________________
For this work Macamine.TM. SO was predissolved by adding 15% isopropanol. For the compositions containing Igepal.TM. 430 or polyvinyl alcohol, 1.6 g/L of Igepal.TM. CO-887 was added to obtain a homogeneous solution. Results are shown in Table 8. Among the candidate materials shown in Table 8, oxa-acid esters such as those identified in the table as OAE 1-4, are preferred lubricant and surface conditioner formers, as are the ethoxylated castor oil derivatives and amine oxides with hydroxyethyl groups bonded to the amine oxide nitrogen, such as Aromox.TM. C/12 and T/12. Quaternary ammonium salts, such as the ETHOQUAD.TM. materials exemplified in Table 7 are also in the preferred group. The ethoxylated castor oil derivatives, amine oxides, and quaternary salts are all considered in more detail below.
7.4 Ethoxylated Castor Oil FRME's
The CCW was charged and operated as described in .sctn.7.3 with the exceptions that the Stage 3 deionized water rinse was applied for 130 sec and the first oven treatment was performed at 200.degree. C. rather than 150.degree. C. The Stage 4 compositions were as shown in Table 9. The experiment using Trylox.TM. 5921 included 0.2 g/L of Igepal.TM. CO-887 in an unsuccessful attempt to clarify the solution; a slight cloudiness persisted even in the presence of the cosurfactant.
TABLE 8 CANDIDATE FINAL RINSE MOBILITY ENHANCERS AND COMPARISONS Mole- Candidate cular COF COF-2 or Comparison Chemical Class Hydrophobe Hydrophile Weight HLB Mean StD Mean StD IFH PFH WBF None -- -- -- -- -- 1.168 .108 1.126 .071 -- -- 32 None -- -- -- -- -- 1.098 .129 -- -- -- -- -- None -- -- -- -- -- 1.141 .151 -- -- -- -- 32 None -- -- -- -- -- 1.331 .263 -- -- -- -- 32 None -- -- -- -- -- 1.362 .194 -- -- -- -- 32 None -- -- -- -- -- 1.295 .197 -- -- -- -- 32 Surfynol .TM. 420 Acetylenic-EO TMDD (EO)1.3 -- 4 1.363 .201 -- -- 59 50 32 Surfynol .TM. 440 Acetylenic-EO TMDD (EO)3.5 -- 8 1.404 .276 -- -- 56 51 32 Surfynol .TM. 465 Acetylenic-EO TMDD (EO)10 -- 13 1.623 .549 -- -- 70 53 31.8 Dimethylformamide Amide -- -- 73.1 -- 1.371 .181 -- -- 56 50 32 Monamine .TM. AD-100 Amide -- -- -- -- .457 .020 .645 .127 74 73 32 M-Pyrol .TM. Amine -- -- -- -- 1.184 .172 -- -- 53 51 32 Macamine .TM. C-10 Amine -- -- -- -- 1.645 .476 -- -- 64 50 32 Triethanolamine Amine -- -- -- -- 1.134 .120 -- -- 53 51 32 Armox .TM. T/12 Amine Oxide C12 (tallow) N.dbd.O/2-hydroxyethyl 366 -- .548 .129 .672 .107 -- -- 32 Aromox .TM. C/12 Amine Oxide C12 (coco) N.dbd.O/2-hydroxyethyl -- -- .527 .090 1.005 .190 77 71 32 Aromox .TM. DM-16 Amine Oxide C16 -- -- -- 1.519 .202 -- -- 54 54 32 Macamine .TM. CAO Amine Oxide Cocamidopropyl N.dbd.O -- -- 1.532 .468 -- -- 70 64 32 Macamine .TM. CO Amine Oxide Cocamine N.dbd.O -- -- 1.329 .222 -- -- 51 50 32 Macamine .TM. SO Amine Oxide Stearamine N.dbd.O -- -- 1.180 .116 -- -- 76 73 32 Triton .TM. RW-100 Amine-(EO)10 -- -- -- 16 .802 .179 1.136 .132 69 61 32 Triton .TM. RW-50 Amine-(EO)5 -- -- -- 13 1.099 .096 -- -- 69 66 32 Triton .TM. RW-75 Amine-(EO)7.5 -- -- -- 15 1.001 .130 1.496 .430 71 62 32 TEA Oleate Amine-Fatty -- -- -- -- 1.214 .438 1.430 .315 52 50 32 Armeen .TM. Z Amphoteric C12 RCOOH/NH -- -- .660 .182 1.463 .299 71 64 32 APG .TM. 300 Glycoside -- -- -- -- 1.146 .201 -- -- 75 66 32 APG .TM. 325 Glycoside -- -- -- -- 1.015 .251 1.211 .183 72 70 32 Hostacor .TM. BF Borate -- -- -- -- 1.211 .157 -- -- 53 51 32 Hostacor .TM. BS Borate -- -- -- -- 1.339 .231 -- -- 58 54 32 OAE-1 C-18 EO/PO C-18/PO(1) (EO)5 -- -- .315 .040 .343 .032 -- -- 32 OAE-2 C16-18 EO C16-18 (EO)5 -- -- .305 .030 .386 .066 -- -- 28 OAE-3 C8-10 EO C8-10 (EO)5 -- -- .602 .149 .687 .118 -- -- 32 OAE-4 C8-18 EO C8-18 (EO)5 -- -- .282 .017 .483 .071 -- -- 16 Acrysol .TM. LMW-45 Carboxylic Acid n/a RCOO(-) 4500 -- 1.102 .112 -- -- 53 50 32 Aminohexanoic Acid Carboxylic Acid C6 RCOOH/NH2 -- -- 1.491 .495 -- -- 50 50 32 Citric Acid Carboxylic Acid -- -- 191.1 -- 1.334 .110 -- -- 55 50 32 Gantrez .TM. S-95 Carboxylic Acid -- -- -- -- 1.353 .356 -- -- 59 52 32 Gluconic acid Carboxylic Acid -- COOH/C--OH -- -- 1.551 .316 -- -- 50 50 32 Isoascorbic Acid Carboxylic Acid -- -- -- -- 1.251 .201 -- -- 51 50 32 Mirawet .TM. B Carboxylic Acid C4 -- -- -- 1.299 .294 -- -- 59 52 32 Potassium Biphthalate Carboxylic Acid -- -- 204.2 -- 1.500 .406 -- -- 53 50 32 Sodium Glucoheptonate Carboxylic Acid -- C--OH/RCOO(-) 249.2 -- 1.238 .122 -- -- 51 51 32 Sodium Gluconate Carboxylic Acid -- C--OH/RCOO(-) 218 -- 1.329 .147 -- -- 51 50 32 Tartaric Acid Carboxylic Acid -- -- -- -- 1.501 .322 -- -- 52 50 32 Chemquat .TM. SP-10 Cationic -- -- -- -- .990 .125 1.538 .162 56 51 32 Tetronic .TM. 701 EO/PO (PO)2.04 (EO)13.7 3600 1-7 .972 .244 2.129 .363 64 51 32 Henkel .TM. SF-7063 EO/PO/Me-ester C13/CH.sub.2 --C(.dbd.O)OCH.sub.3 (EO)8.5 -- -- .287 .038 .374 .049 -- -- 32 Ethox .TM. MI-14 Ester C18 (EO)14 -- 13 .402 .044 .474 .048 70 67 32 Ethox .TM. MI-14 Ester C18 (EO)14 -- 13 .492 .076 .558 .146 -- -- 32 Ethox .TM. MI-14 Ester C18 (EO)14 -- 13 .426 .042 .708 .133 68 67 32 Ethox .TM. MI-14 Ester C18 (EO)14 -- 13 .458 .080 .841 .241 67 63 32 Ethox .TM. MI-14 Ester C18 (EO)14 -- 13 .455 .087 .841 .274 66 64 32 Ethox .TM. MI-14 Ester C18 (EO)14 -- 13 .432 .061 -- -- 67 63 32 Ethox .TM. MI-14 Ester C18 (EO)14 -- 13 .468 .090 -- -- -- -- -- Brij .TM. 30 Fatty Alcohol C12 (EO)4 -- -- .890 .161 1.013 .076 -- -- 32 Chemal .TM. 2EH5 Fatty Alcohol 2-ethylhexanol (EO)2 -- -- 1.032 .068 1.075 .103 -- -- 32 Chemal .TM. PA-5P8 Fatty Alcohol C-10 LA/PO EO -- -- .815 .200 .725 .132 57 50 32 Ethal .TM. 2EH2 Fatty Alcohol 2-ethyl hexanol (EO)2 -- 8.1 1.167 .118 1.149 .146 -- -- 32 Ethal .TM. CSA-10 Fatty Alcohol C16-18 (EO)12 -- -- .748 .164 .761 .166 high -- 32 Ethal .TM. CSA-17 Fatty Alcohol C16-18 (EO)17 -- -- .726 .177 .677 .167 -- -- 32 Ethal .TM. DA-6 Fatty Alcohol C10 (EO)6 -- 12.4 .931 .201 1.045 .155 -- -- 32 Ethal .TM. OA-23 Fatty Alcohol C18 (EO)23 -- 15.8 .698 .175 .749 .192 -- -- 32 Ethal .TM. TDA-6 Fatty Alcohol C13 (EO)6 -- 11.4 .764 .179 .930 .163 -- -- 32 Sandoxylate .TM. SX-408 Fatty Alcohol i-C10-12 LA/PO EO -- 11 .913 .107 .885 .105 -- -- 32 Sandoxylate .TM. SX-424 Fatty Alcohol i-C10-12 LA/PO EO -- 15 .688 .160 .676 .137 -- -- 32 Sandoxylate .TM. SX-602 Fatty Alcohol i-C10-12 LA/PO EO -- 8 .966 .132 1.145 .175 -- -- 32 Triton .TM. XL-80N Fatty Alcohol C8-10 EO/PO/EO EO 420 -- .801 .187 .776 .156 -- -- 32 Varonic .TM. MT-42 Fatty Alcohol C12-18 CH3 cap EO -- -- .549 .093 .581 .156 -- -- 32 Varonic .TM. MT-48 Fatty Alcohol C12-18 CH3 cap EO -- -- .583 .146 .692 .180 -- -- 32 Varonic .TM. MT-65 Fatty Alcohol C12-18 CH3 cap EO -- -- .814 .171 .862 .122 -- -- 32 Fluorad .TM. FC-126 Fluorosurfactant C7F15 R--COONa -- -- 1.335 .233 -- -- 65 50 0 Kelig .TM. 100 Ligno-Sulfonate -- -- -- -- 1.450 .473 -- -- 53 50 32 Kelig .TM. 400 Ligno-Sulfonate -- -- -- -- 2.022 .773 -- -- 54 51 32 Igepal .TM. 660 NP--(EO)10 Nonyl Phemol (EO)10 660 13.2 1.527 .555 -- -- 70 65 32 Igepal .TM. 710 NP--(EO)10.4 Nonyl Phenol (EO)10.4 678.5 13.6 1.330 .329 -- -- 75 67 32 Igepal .TM. 720 NP--(EO)12 Nonyl Phenol (EO)12 748 14.2 1.524 .423 -- -- 76 71 32 Igepal .TM. 430 NP--(EO)4 Nonyl Phenol (EO)4 396 8.8 .516 .064 .815 .195 63 60 32 Igepal .TM. 610 NP--(EO)7.5 Nonyl Phenol (EO)7.5 570.9 12.2 .693 .170 1.021 .176 63 60 32 Carbowax .TM. Methoxy PEG PEG O--CH3 (EO)44.7 2000 -- .766 .222 .886 .199 -- -- 32 Carbowax .TM. Methoxy PEG PEG O--CH3 (EO)7.3 350 -- .955 .126 1.047 .113 -- -- 32 Carbowax .TM. Methoxy PEG PEG O--CH3 (EO)112.8 5000 -- .739 .158 .839 .118 -- -- 32 Carbowax .TM. Methoxy PEG PEG O--CH3 (EO)16.3 750 -- .927 .236 .915 .190 -- -- 32 Carbowax .TM. PEG 20M PEG -- (EO)n 17500 -- .663 .149 .934 .155 -- -- 32 Carbowax .TM. PEG-1450 PEG -- (EO)32.5 1450 -- .778 .158 .854 .229 -- -- 32 Carbowax .TM. PEG-200 PEG -- (EO)4.15 200 -- 1.122 .140 1.050 .114 -- -- 32 Carbowax .TM. PEG-3350 PEG -- (EO)75.7 3350 -- .747 .105 .921 .149 -- -- 32 Carbowax .TM. PEG-8000 PEG -- (EO)181.2 8000 -- .778 .188 .840 .162 -- -- 32 Carbowax .TM. PEG-900 PEG -- (EO)19.5 900 -- .819 .199 .865 .212 -- -- 32 Dequest .TM. 2000 Phosphonate -- N[CH2--P.dbd.O(OH).sub.2 ].sub.3 299 -- 1.506 .203 -- -- 52 50 32 Dequest .TM. 2006 Phosphonate -- Na.sub.5 N[CH.sub.2 --P.dbd.O(OH).sub.2 ].sub.3 409 -- 1.327 .095 -- -- 51 51 32 Dequest .TM. 2016 Phosphonate -- [(C--CH.sub.3 OH)][P.dbd.O(Na).sub.2 ].sub.2 294 -- 1.271 .209 -- -- 51 51 32 Dequest .TM. 2054 Phosphonate -- HMDA[CH.sub.2 --P.dbd.O(Na).sub.2 ].sub.4 721 -- 1.095 .225 -- -- 51 50 32 Dequest .TM. 2066 Phosphonate -- Trien[CH.sub.2 --P.dbd.O(Na).sub.2 ] 683 -- 1.176 .150 -- -- 51 50 32 Belzak .TM. AC Polyhydric -- R--OH -- -- 1.211 .098 -- -- 52 50 32 Cerelose .TM. 2001 Polyhydric -- -- -- -- 1.318 .095 -- -- 51 50 32 Glycerine Polyhydric -- -- -- -- 1.335 .134 -- -- 51 50 32 Hexylene glycol Polyhydric 2-Me,2,4-C5 diol (C-- OH)2 -- -- 1.886 .130 -- -- 58 50 32 Methocel .TM. 40-200 Polyhydric -- -- -- -- .901 .076 1.193 .252 60 54 32 Pentaerythritol Polyhydric -- -- -- -- 1.133 .088 -- -- 54 52 32 Poly{vinyl alcohol} Polyhydric -- -- -- -- .479 .067 .982 .420 71 67 32 Sorbitol Polyhydric -- C--OH 182 -- 1.239 .091 -- -- 51 50 32 Tripropylene Glycol Polyhydric -- -- -- -- 1.266 .125 -- -- 60 52 32 Xanthan Gum Polyhydric -- -- -- -- 1.059 .139 -- -- 52 51 32 SOMAT .TM. Proprietary -- -- -- -- .714 .161 -- -- -- -- -- Tween .TM. 20 Sorbitan ester-(EO).sub.20 C12 EO -- -- .601 .100 1.146 .498 59 68 32 Dodecylbenzene Sulfonate Sulfonate C12--Ph SO3(-) -- -- .396 .029 .616 .182 100 82 8.5 Dowfax .TM. 2Al Sulfonate iso-C12--Ph (bis) [SO3(-)]2 576 -- .614 .112 .793 .109 71 68 0 Heptane Sulfonate Sulfonate C6 C6-COOH -- -- 1.214 .436 -- -- 52 50 32 Nacconol .TM. 90F Sulfonate -- -- -- -- .387 .021 .462 .065 100 95 Notes for Table 8 "StD" here and in subsequent tables means "standard deviation from the mean." "WBF" means "waterbreak free rating". The multiple entries for "None" and for Ethox .TM. MI14 represent determinations with different lots of cans. The "OAE" products have the general chemical formula: RO--(C.sub.3 H.sub.6 O).sub.m --(C.sub.2 H.sub.4 O).sub.n --CH.sub.2 --C(O)O--CH.sub.3, with the straight chain alkyl group R ranging from 8 to 18 carbon atoms i length, "m" being 0 or 1, and "n" ranging from 5 to an average of 8.5.
TABLE 9______________________________________ETHOXYLATED HYDROGENATED CASTER OILDERIVATIVES AND COMPARISONS AS FINALRINSE MOBILITY ENHANCERSProduct Grams/ COF COF-2Name 8 Liters Mean StD Mean StD IFH PFH______________________________________None 0 1.231 .149 -- -- -- --Trylox .TM. 1.6 .479 .072 .503 .085 69 655922Trylox .TM. 0.4 .974 .161 1.055 .151 60 565922Trylox .TM. 0.8 1.007 .117 1.131 .132 70 605922Trylox .TM. 1.6 .511 .108 .548 .093 74 685921Trylox .TM. 0.4 1.072 .144 1.034 .201 63 595921Trylox .TM. 0.8 .883 .154 .958 .152 62 545921Trylox .TM. 3.2 .914 .140 1.139 .157 67 625925Trylox .TM. 6.4 1.020 .149 1.231 .122 74 675925Trylox .TM. 9.6 .965 .180 1.007 .122 73 635925Ethox .TM. 1.6 .621 .118 1.059 .144 75 70MI-14______________________________________
7.5 The Effect of Ethylene Oxide Content On The Properties of lsostearyl FRME's And Binary Mixtures With Other Surfactants
The CCW was charged and operated as described in .sctn.7.3 with the Stage 4 variations shown in Table 10. The results in Table 10 indicate that only very slight defoaming at best was achievable with these defoamers. However, lower amounts of ethoxylation of the primary ethoxylated iso-stearic acid lubricant and surface conditioner forming composition result in less foam, with COF values that are fully adequate for most applications. Mixtures of the "defoamers" Pluronic.TM. 31R1 and Trycol.TM. 6720 with Ethox.TM. MI-9 produced somewhat more foam than compositions with an equal total amount of Ethox.TM. MI-9 alone, but also give further reductions in the COF. The interactions are evidently complex and difficult to predict.
TABLE 10______________________________________EFFECT OF VARIATION OF DEGREE OFETHOXYLATION IN PRIMARY LUBRICANT ANDSURFACE CONDITIONER (ETHOXYLATED ISOSTEARICACID) AND OF VARIATION OF COSURFACTANTADDED AS ATTEMPTED DEFOAMER Ethoxylated Isostearic Acid # of EOCOF per DefoamerMean StD g/8L Molecule g/8L Name IFH PFH______________________________________1.139 .170 0 -- 0 -- -- --1.159 .181 0 -- 0 -- -- --1.069 .165 0 -- 0 -- -- --1.190 .158 0 -- 0 -- -- --1.154 .198 0 -- 0 -- -- --1.142 .174 (Average of result with above five can lots).587 .170 0 -- 1.60 Pluronic .TM. 77 50 31R1.817 .155 0 -- 1.60 Triton .TM. 79 55 DF-16.659 .175 0 -- 1.60 Trycol .TM. 50 50 LF-1.499 .099 1.60 9 0 -- 55 55.478 .072 1.20 9 .40 Pluronic .TM. 61 58 31R1.479 .093 1.20 9 .40 Triton .TM. 63 62 DF-16.423 .027 1.20 9 .40 Trycol .TM. 69 67 LF-1.408 .038 .80 9 .80 Pluronic .TM. 65 63 31R1.576 .172 .80 9 .80 Triton .TM. 72 69 DF-16.467 .103 .80 9 .80 Trycol .TM. 65 63 LF-1.496 .122 .40 9 1.20 Pluronic .TM. 67 64 31R1.628 .176 .40 9 1.20 Triton .TM. 78 76 DF-16.656 .194 .40 9 1.20 Trycol .TM. 73 66 LF-1.457 .074 1.60 10.5 0 -- 60 60.465 .121 1.20 10.5 .40 Pluronic .TM. 60 59 31R1.531 .108 1.20 10.5 .40 Triton .TM. 67 66 DF-16.566 .186 1.20 10.5 .40 Trycol .TM. 65 65 LF-1.583 .114 .80 10.5 .80 Pluronic .TM. 58 57 31R1.564 .142 .80 10.5 .80 Triton .TM. 72 72 DF-16.550 .114 .80 10.5 .80 Trycol .TM. 69 65 LF-1.539 .111 .40 10.5 1.20 Pluronic .TM. 55 53 31R1.685 .205 .40 10.5 1.20 Triton .TM. 75 70 DF-16.644 .133 .40 10.5 1.20 Trycol .TM. 77 62 LF-1.444 .104 1.60 14 0 -- 76 75.477 .098 1.60 14 0 -- 77 75.534 .093 1.20 14 .40 Pluronic .TM. 74 71 31R1.456 .121 1.20 14 .40 Triton .TM. 80 75 DF-16.516 .148 1.20 14 .40 Trycol .TM. 81 80 LF-1.505 .106 .80 14 .80 Pluronic .TM. 82 79 31R1.532 .128 .80 14 .80 Triton .TM. 85 84 DF-16.456 .078 .80 14 .80 Trycol .TM. 86 83 LF-1.681 .178 .40 14 1.20 Pluronic .TM. 82 79 31R1.615 .149 .40 14 1.20 Triton .TM. 81 78 DF-16.538 .106 .40 14 1.20 Trycol .TM. 80 76 LF-1______________________________________
7.6 Final Rinse Mobility Enhancers and Water Drainage Aids
The BW was operated as follows:
______________________________________Stage 1 sulfuric acid, pH 2.0, 54.4.degree. C.Stage 2 RIDOLINE 124C, 15 mL Free Acid, 3.4 g/L of total surfactant, Fluoride Activity -10 mV, 60.degree. C.Stage 3 tap waterStage 4 not usedStage 5 deionized waterStage 6 as noted in Table 11, 0.2 g/L of total active additive.______________________________________
TABLE 11__________________________________________________________________________VARIATION OF WATER DRAINAGE WITH LINE SPEEDAND ADDITIVE TO FINAL RINSE Line WaterLubricant and/or Water Speed Retention COF COF-2Drainage Promoting Additive Setting Mean StD Mean StD (Mean)__________________________________________________________________________None 100 31.72 -- -- -- --None 100 30.44 -- -- -- --None 70 28.40 -- -- -- --None 70 28.29 .81 1.446 .071 --None 70 27.02 1.00 -- -- --None 40 23.34 -- -- -- --Ethox .TM. MI-14 40 19.11 -- -- -- --Neodol .TM. 91-2.5 70 15.65 .37 1.356 .211 --Pluronic .TM. L-81 70 17.44 .14 1.124 -- --Pluronic .TM. L-61 70 17.71 .09 1.206 -- --Neodol .TM. 91-6 70 20.83 .27 1.201 .175 --Ethox .TM. MI-14/ 70 21.02 .53 .728 -- .970Pluronic .TM. L-81 (1:1)Ethox .TM. MI-14/ 70 21.63 .32 .725 -- .832Pluronic .TM. L-61 (1:1)Ethal .TM. OA-23 70 21.64 .72 .919 -- 1.141Ethox .TM. MI-14 70 21.68 .18 -- -- --Ethox .TM. MI-14 70 21.69 -- -- -- --Ethox .TM. MI-10.5 70 21.93 .38 .550 -- .727Neodol .TM. 91-8 70 22.55 .30 1.009 .204 --Ethox .TM. MI-14/ 70 24.07 1.00 .581 -- .707Trylox .TM. 5922 (1:1)Trylox .TM. 5925 70 24.62 .92 1.090 -- --Trylox .TM. 5922 70 25.21 .97 .581 -- .680Trylox .TM. 5921 70 25.88 .26 .546 -- .645Ethox .TM. MI-14 100 26.60 -- -- -- --__________________________________________________________________________
The line speed of this washer was controlled by a rheostat with the following approximate relationship between percentage of output and line speed in feet per minute:
______________________________________Setting: 100% Speed: 6.2 fpm 70 3.4 fpm 40 1.8 fpm.______________________________________
Three sets of 14 cans each were treated and collected at the end of the washer using tongs. The cans were stacked on a light gauge aluminum baking pan and weighed with the tongs taking care to lose as little water as possible during the manipulations. The cans, tongs and tray were then dried at 210.degree. C. for ten minutes and reweighed. The average of three replicate runs was taken as an estimation of the water retention of the finished cans. A fourth set of cans was collected, dried at 210.degree. C. for 3 minutes and tested to determine their COF. For those cases where the COF was less than 1.00 the COF-2 was determined. Results are shown in Table 11. Some surfactants were found that are better at promoting water drainage than the ethoxylated isostearic acids that are very effective in providing lubricant and surface conditioner films. However, the surfactants that are exceptionally good at promoting water drainage are much poorer than ethoxylated isostearic acids in reducing COF. Mixing the two types permits improvement in water drainage, while retaining the ability to achieve COF values that are adequate in many applications.
7.7. Amine Oxide and/or Quaternary Ammonium Salt Combinations with Fluoride
General Conditions for the Examples and Comparison Examples in .sctn.7.7
All the process examples and comparison examples described below in this section used aluminum cans as substrates and a laboratory prototype simulation-of a commercial six stage processor. Each run was made with 14 cans. The process sequence used is described in Table 12.
Stage 4 compositions were prepared either by dilution of concentrate or directly from the ingredients. In order to simulate what happens in a commercial can washing operation, the aluminum level (i.e., the stoichiometric equivalent as aluminum of the total of components (D) and (E) above) was adjusted to about 100 ppm, to account for Stage 3 drag-out into Stage 4. Additionally, the pH, fluoride activity, and concentrations of other components varied with the particular experiment, as described specifically below.
Cans washed and rinsed according to the six stage process described above were dried for 5 minutes at 150.degree. C. under normal conditions, except that when heat resistant
TABLE 12______________________________________Times in Seconds for: Temp.,Stage Spray Dwell Blow-Off .degree.C. Composition______________________________________1 30 10 30 54.4 Aqueous H.sub.2 SO.sub.4 to give pH = 2.2 90 10 30 60.0 See Notes for this table below.3 30 10 30 22 .+-. 4 Tap Water4 20 20 30 37.8 Varies; see details below.5 30 0 0 22 .+-. 4 Tap water rinse6 90 0 30 22 .+-. 4 DI water rinse______________________________________ Notes for Table 12 The composition for Stage 2 contained (i) a commercially available sulfuric acid and surfactant cleaner (RIDOLINE .RTM. 124C from PA) at a concentration to give 3.4 grams per liter of total surfactant and (ii) hydrofluoric acid, and if needed, additional sulfuric acid to give a free acid value of 15 points and a fluoride ion activity reading of -10 mv, using the Orion instrument and associated electrodes as described in the main text above. The free acid points are determined by titrating a 10 mL sample of the composition, dissolved in about 100 ml of distilled water, with 0.10 N NaOH solution, using a phenolphthalein indicator after dissolving a large excess of sodium fluoride (about 2-3 ml in bulk volume of powdered dry reagent) in the sample before titrating. The points of free acid are equal to the number of mL of titrant required to reach a faint pink end point.
mobility was being tested, the cans were subsequently placed in a 200.degree. C. oven for an additional 5 minutes. These conditions were identified as single and double baked cans, respectively.
All determinations of coefficient of friction were made in the manner described in lines 44-65 of U.S. Pat. No. 4,944,889 and were the average of 15 individual measurements.
The domes were removed from the cans using a can opener. Once this was done, they were placed in a 66.degree. C. water bath containing 0.2 grams of sodium tetraborate decahydrate per 1000 mL of deionized water. Following immersion for 30 minutes, the domes were rinsed with DI water and dried in an oven. The quality of resistance to dome staining was judged on a visual basis with cleaned only (non treated) cans as a negative control and cans treated with Alodine.RTM. 404 as a positive control. Both the exterior and interior dome surfaces were inspected.
Example and Comparison Example Group 7.7.1
In this group, component (A) as described above was Aromox.RTM. C/12, which according to its supplier is an amine oxide with a chemical structure represented by:
Cocoa-N(O)(CH.sub.2 CH.sub.2 OH).sub.2,
where "Cocoa" represents the mixture of alkyl groups that would result by substituting a --CH.sub.2 -- moiety for each --COOH moiety in the mixture of fatty acids obtained upon hydrolysis of natural coconut oil.
The values of the variables in this group of experiments are shown in Table 13, and the particular combinations of these variables tested and the resulting coefficients of friction on the cans treated are shown in Table 14.
TABLE 13______________________________________ Values of the Variables:Variable High Medium Low______________________________________H.sub.2 ZrF.sub.6.sup.1 0.0099 0.0069 0.0040pH 4.50 3.50 2.50Molar Ratio of 2.0 1.0 0.0H.sub.3 PO.sub.4 to H.sub.2 ZrF.sub.6Molar Ratio of 1.0 0.75 0.5AO.sup.2 to H.sub.2 ZrF.sub.6______________________________________ Notes for Table 13 .sup.1 Values shown are moles in 8 liters of composition. .sup.2 "AO" means "amine oxide", in this case Aromox .RTM. C/12.
TABLE 14______________________________________Value.sup.1 for Variable in Runwith This Number:Run [H.sub.3 PO.sub.4 ]/ [AO]/ COF-No. H.sub.2 ZrF.sub.6 pH [H.sub.2 ZrF.sub.6 ] [H.sub.2 ZrF.sub.6 ] COF-SB.sup.2 DB.sup.3______________________________________ 1 0 0 0 0 0.739 0.874 2 -1 +1 +1 +1 1.421 -- 3 +1 +1 -1 +1 0.728 0.712 4 -1 -1 -1 +1 1.065 1.189 5 +1 -1 -1 +1 0.565 0.638 6 0 0 0 0 0.582 0.578 7 +1 -1 +1 -1 1.366 -- 8 -1 -1 +1 +1 1.410 -- 9 +1 -1 +1 +1 0.605 0.58110 -1 +1 -1 +1 0.781 0.88511 0 0 0 0 1.046 --12 -1 -1 +1 -1 1.547 --13 +1 +1 +1 +1 1.459 --14 -1 -1 -1 -1 1.312 --15 +1 +1 -1 +1 0.609 0.58816 0 0 0 0 0.606 0.64717 -1 +1 +1 -1 1.410 --18 +1 +1 +1 -1 1.470 --19 +1 -1 -1 -1 0.550 0.59320 -1 +1 -1 -1 1.400 --21 0 0 0 0 0.828 0.880______________________________________ Footnotes for Table 14 .sup.1 The value is expressed as high ("+1"), medium ("0"), or low ("-1") with the numerical meanings for these values given in Table 13. .sup.2 "SB" = single bake. .sup.3 "DB" = double bake
Example and Comparison Example Group 7.7.2
In this group quaternary ammonium salts were used instead of the amine oxide in Group 1. The particular salts used are shown in Table 15.
TABLE 15__________________________________________________________________________QUATERNARY AMMONIUM SALTS Chemical Structure of:Trademark Name Cation Counter Ion__________________________________________________________________________ETHOQUAD .RTM. C-12 ##STR2## Cl.sup.-ETHOQUAD .RTM. C-12B ##STR3## Cl.sup.-ETHOQUAD .RTM. T-13/50 ##STR4## --OC(O)CH.sub.3__________________________________________________________________________ Notes for Table 15 "Cocoa" here means the same mix of alkyl groups as already noted in the main text, while "Tallow" means the same as "Cocoa" except that animal tallow is substituted for coconut oil in the definition given. ".PHI." represents a phenyl moiety.
All the Stage 4 compositions in this group contained 9.6 grams of Al.sub.2 (SC).sub.4).sub.3.151/2H.sub.2 O (which corresponds to 104 ppm of Al.sup.+3), 2.05 grams of H.sub.2 ZrF.sub.6, and 0.0099.+-.0.0001 mole of quaternary ammonium salt; those compositions designated with "/PA" in Table 16 below also had 0.97 grams of H.sub.3 PO.sub.4, all in 8 liters of total composition. The compositions all had a pH value of 2.5. The results of the treatments as described are shown in Table 16 below.
TABLE 16______________________________________Quat in Composition Free F.sup.-1 COF-SB COF-DB DS______________________________________ETHOQUAD .RTM. C-12 -89.0 1.12 1.28 3ETHOQUAD .RTM. C-12/PA -90.0 0.69 0.87 3ETHOQUAD .RTM. C-12B -93.1 0.98 1.21 3ETHOQUAD .RTM. C-12B/ -89.9 0.90 0.94 3PAETHOQUAD .RTM. T-13/50 -84.0 0.85 0.98 3ETHOQUAD .RTM. T-13/50/ -90.3 0.49 0.53 2PA______________________________________ Notes for Table 16 The column headed "Free F.sup.-1 " gives the readings for the composition in millivolts, using an Orion Fluoride Sensitive Electrode and apparatus standardized with 120E Activity Standard Solution as described above. The column headed "DS" gives dome stain resistance evaluations on the following scale: 1 = Better (less staining) than with ALODINE .RTM. 404; = Equal staining as when using ALODINE .RTM. 404; 3 = As much staining as with no additive in Stage 4 (worse than with ALODINE .RTM. 404. "COFSB" = coefficient of friction with single bake, and "COFDB" = coefficient of friction with double bake.
Example and Comparison Example Group 7.7.3
In this group, only ETHOQUAD.RTM. T-13/50 was used as component (A), and only H.sub.2 ZrF.sub.6 was used as component (B). In addition to concentration of the ETHO-QUAD.RTM. T-13/50, the other variables investigated were H.sub.2 ZrF.sub.6 concentration, pH, and nitrate versus sulfate anions in solution. In order to adjust pH and free F.sup.-, it was found advantageous to use sodium aluminate as a partial source of aluminum. In all compositions in this group, sodium aluminate at a concentration of 50 ppm as Al was used along with phosphoric acid in an amount equimolar with the H.sub.2 ZrF.sub.6 used; fluoride activity was adjusted to a reading of -90 mv on fluoride sensitive electrode as described above. An additional 50 ppm of Al was added as (i) aluminum sulfate, in which case sulfuric acid was used to adjust the pH; (ii) as aluminum nitrate, in which case nitric acid was employed to adjust the pH; or (ii) both aluminum nitrate and aluminum sulfate were added, in which case both acids, in the same molar ratio as their corresponding aluminum salts, were used to adjust the pH. The results are reported in detail below. The four variables tested and the three values of each such variable are shown in Table 17, and the combinations of the values of the three variables and the results are shown in Table 18.
TABLE 17______________________________________ Values for Variable:Variable and Designator High Medium Low______________________________________ Moles of H.sub.2 ZrF.sub.6X1 = in 8 liters of 0.009 0.00675 0.0045 compositionX2 = pH 3.1 2.8 2.5 Molar percent of theX3 = aluminum salt(s) 100 50 0 that was aluminum nitrate Molar ratio ofX4 = ETHOQUAD .RTM. 1.00 0.75 0.5 T-13/50 to H.sub.2 ZrF.sub.6______________________________________
TABLE 18__________________________________________________________________________Run No. X1 X2 X3 X4 COF-SB COF-DB DS__________________________________________________________________________ 1 1 -1 -1 -1 0.513 0.531 2 2 1 1 1 1 0.544 0.700 3 3 1 1 -1 -1 1.274 1.406 3 4 0 0 0 0 0.499 0.629 3 5 -1 -1 1 -1 0.508 0.517 2 6 0 0 0 0 0.572 0.731 2 7 0 0 0 -1 1.229 1.257 3 8 -1 1 1 -1 1.421 1.397 3 9 0 0 1 0 0.516 0.700 210 -1 1 -1 -1 1.451 1.458 311 1 1 1 -1 1.311 1.412 312 1 1 -1 1 0.976 1.149 313 0 0 0 1 0.501 0.549 214 -1 1 1 1 0.762 1.049 315 1 -1 1 -1 0.552 0.553 116 0 -1 0 0 0.537 0.553 217 1 -1 1 1 0.559 0.592 118 0 1 0 0 1.158 1.346 319 1 -1 -1 1 0.522 0.561 120 0 0 0 0 0.599 0.813 321 -1 0 0 0 0.484 0.518 222 0 0 0 0 0.619 0.732 323 -1 1 -1 1 0.738 0.998 324 1 0 0 0 0.732 0.913 325 0 0 0 0 0.581 0.875 326 -1 -1 -1 1 0.520 0.546 227 -1 -1 1 1 0.511 0.518 228 -1 -1 -1 -1 0.503 0.532 229 0 0 0 0 0.610 0.673 2__________________________________________________________________________ Notes for Table 18 In the columns headed "X1", "X2", "X3", and "X4", the entry "+1" indicate the high value for the variable as specified in Table 17; the entry "0" indicates the middle value for the variable as specified in Table 17; and the entry "-1" indicates the low value for the variable as specified in Table 17. Other column headings and meanings are the same as in Table 16.
Example and Comparison Example Group 7.7.4
In this group, the general conditions and materials used were the same as for Group 7.7.3 except that in all cased in this group, aluminum sulfate and sulfuric acid were used and no aluminum nitrate or nitric acid was used, but the values of the some of the variables were different. The various combinations and the resulting performance are shown in Table 19.
TABLE 19__________________________________________________________________________Concentration in Mil-Run moles per 8 Liters of: MolarNo. pH H.sub.2 ZrF.sub.6 H.sub.3 PO.sub.4 T13.sup.2 Ratios.sup.1 COF-SB COF-DB DS__________________________________________________________________________ 1 CLEAN 1.155 -- 3.0 ONLY 2 2.00 9.00 9.00 4.50 1:1:0.5 0.543 0.582 3.0 3 2.20 9.00 9.00 4.50 1:1:0.5 0.546 0.551 2.0 4 2.50 9.00 9.00 4.50 1:1:0.5 0.505 0.492 2.0 5 2.50 9.00 0.00 4.50 1:0:0.5 0.584 0.576 3.0 6 2.50 9.00 4.50 2.25 1:0.5:0.25 0.512 0.557 3.0 7 2.50 9.00 4.50 9.00 1:0.5:1 0.522 0.545 2.0 8 2.50 9.00 4.50 18.00 1:0.5:2 0.479 0.509 2.0 9 2.50 9.00 18.00 2.25 1:2:0.25 0.511 0.531 2.010 2.50 9.00 18.00 9.00 1:2:1 0.514 0.513 2.011 2.50 9.00 18.00 18.00 1:2:2 0.466 0.491 1.512 2.50 4.50 2.25 1.13 1:0.5:0.25 0.481 0.496 2.513 2.50 4.50 2.25 4.50 1:0.5:1 0.485 0.528 3.014 2.50 4.50 2.25 9.00 1:0.5:2 0.468 0.509 3.015 2.50 4.50 9.00 1.13 1:2:0.25 0.531 0.577 2.516 2.50 4.50 9.00 4.50 1:2:1 0.475 0.480 2.017 2.50 4.50 9.00 9.00 1:2:2 0.458 0.503 2.018 2.50 13.50 6.75 3.38 1:0.5:0.25 0.515 0.529 2.019 2.50 13.50 6.75 13.50 1:0.5:1 0.497 0.544 1.520 2.50 13.50 6.75 27 1:0.5:2 0.470 0.519 1.521 2.50 13.50 27.00 3.38 1:2:0.25 1.453 1.338 2.022 2.50 13.50 27.00 13.50 1:2:1 0.535 0.595 2.023 2.50 13.50 27.00 27 1:2:2 0.479 0.514 1.524 2.80 9.00 9.00 4.50 1:1:0.5 0.568 0.733 2.025 ALODINE .RTM. 1.463 -- 2.0 404__________________________________________________________________________ Footnotes for Table 19 .sup.1 The ratios are shown in the order: H.sub.2 ZrF.sub.6 :H.sub.3 PO.sub.4 :T13. .sup.2 "T13" means ETHOQUAD .RTM. T13/50. Other Notes for Table 19 The column headings "COFSB", "COFDB", and "DS" and the entries in these columns have the same meanings as in Table 16.
A preferred group of concentrates according to this embodiment of the invention has the following compositions, with water forming the balance of each composition not specified below:
______________________________________ Grams of Ingredient per Kilogram of Concen-Ingredient trate Composition______________________________________Inorganic Make-Up Concentrate45% Fluozirconic acid solution in water 32.375% Phosphoric acid solution in water 9.1Aqueous nitric acid, 42.degree. Baume 25.5Organic Make-Up and Replenisher ConcentrateETHOQUAD .RTM. T-13/50 70.0SURFYNOL .RTM. 104 23.8Inorganic Replenisher Concentrate45% Fluozirconic acid solution in water 44.475% Phosphoric acid solution in water 12.670% Hydrofluoric acid solution in 4.6waterAqueous nitric acid, 42.degree. Baume 38.7______________________________________
The SURFYNOL.RTM. 104 noted above was added for its antifoam activity. It is a commercial product of Air Products and Chemicals Co. and is reported by its supplier to be 2,4,7,9-tetramethyl-5-decyn-4,7-diol.
In a preferred process embodiment of this invention, a working composition was prepared by adding 1% of each of the above noted Make-Up Concentrates to deionized water, and the resulting solution, which had a pH within the range from 2.7 to 2.9 and a fluoride activity value between -60 and -80 mv relative to Standard Solution 120E was used in stage 4 to treat commercially supplied D & I aluminum cans for mobility enhancement by spraying the cans for 25 sec at 43.degree. C. The resulting cans had COF-SB values in the range from 0.5 to 0.6 and dome staining resistance equal to that achieved with ALODINE.RTM. 404, particularly when the aluminum cation concentration in the treating composition was in the range from 100-300 ppm. As the treating composition is used, replenisher compositions as described above are added as needed to maintain the COF and dome staining resistance.
If a one package make-up concentrate is required, the following is an example of a preferred concentrate, with water forming the balance not otherwise stated:
______________________________________ Grams of Ingredient per Kilogram of Concen-Ingredient trate Composition______________________________________Aqueous sulfuric acid, 66.degree. Baume 13.045% Fluozirconic acid solution in water 41.475% Phosphoric acid solution in water 11.670% Hydrofluoric acid solution in 7.7waterETHOQUAD .RTM. T-13/50 40.9______________________________________
In a preferred process embodiment using this concentrate, 50 mL of concentrate was diluted to form 8 liters of working composition, with the pH adjusted if necessary to 2.4-2.6 and the free fluoride activity to -85 to -95 mv. A COF value of less than 0.6 was obtained in several experimental trials over a thirteen week period of storage of the concentrate.
Examples and Comparison Examples Group 8
The combination of ethoxylated castor oil derivatives and fluozirconic acid shown in Table 8 above has been found to have an unexpected additional advantage, which is illustrated further in this group.
An FRME combining fluozirconic acid and hydrogenated castor oil derivatives in proper concentrations has been found to provide both protection against dome staining during pasteurization and adequate lowering of the COF for most purposes.
The can washing setup for this group of examples was:
______________________________________Stage 1 sulfuric acid, pH 2.0, 30 sec., 54.4.degree. C.Stage 2 RIDOLINE .TM. 124C, 15 mL Free Acid, 3.4 g/L total of surfactant, Fluoride Activity -10 mV, 90 sec., 54.4.degree. C.Stage 3 deionized water, 150 sec. (ca. 17.7 L)Stage 4 as noted in Table 7 and below, 20 sec. spray + 20 sec. dwell, 29.4.degree. C. temperatureStage 5 not usedStage 6 not used______________________________________
In addition to the ingredients listed in Table 7, the solutions were all adjusted to pH 4.5 by addition of aqueous ammonia or nitric acid as required.
Dome staining was evaluated by first removing the domes from the treated cans with a can opener. The domes were then placed in a water bath containing 0.2 g/L of borax at 65.6.degree. C. for 30 minutes, then rinsed in deionized water and dried in an oven. Staining resistance was evaluated visually by comparison with known satisfactory and unsatisfactory standards. Results are shown in Table 20. The last two conditions shown in Table 20 are highly satisfactory with respect to both COF and dome staining resistance during pasteurization.
TABLE 20______________________________________EFFECT OF CONCENTRATIONS OF ETHOXYLATEDCASTER OIL DERIVATIVE AND OF FLUOZIRCONICACID ON DOME STAINING RESISTANCE ANDCOEFFICIENT OF FRICTIONGrams of Grams of Trylox .TM. PasteurizationH.sub.2 ZrF.sub.6 /Liter 5921/Liter COF Protection Rating______________________________________0 0 1.16 Fail0 0.2 0.57 Fail0.14 0.2 0.52 Fail0.29 0.2 0.61 Marginal0.58 0.2 0.63 Pass1.16 0.2 0.70 Pass______________________________________
Examples and Comparison Examples Group 9
This group illustrates use with tin cans. Three types of materials were tried as lubricant and surface conditioner forming and water drainage promoting agents for tin cans: (i) Ethox.TM. MI-14; (ii) a combination of 1 part by weight of Pluronic.TM. 31R1 and 4 parts by weight of Plurafac.TM. D25; and (iii) Tergitol.TM. Min-Foam.TM. 1X. Of these, the Ethox.TM., Tergitol.TM., and Plurafac.TM. products are ethoxylated fatty acids or alcohols, with a poly{propylene oxide} block cap on the end of the poly{ethylene oxide} block in some cases, while the Pluronic.TM. is a block copolymer of ethylene and propylene oxides, with poly{propylene oxide} block caps on the ends of the polymers. All were used at a concentration of 0.2 g/L of active material with deionized water in a final rinse before drying, after an otherwise conventional tin can washing sequence. Water retention and COF values were measured as generally described above. Results are shown in Table 21.
TABLE 21______________________________________RESULTS WITH TIN-PLATED STEEL D&I CANS Percent WaterAdditive to Final Rinse Mean COF Value Retention______________________________________None 1.04 100% (Defined)Ethox .TM. 0.70 83.6Pluronic .TM./Plurafac .TM. 0.81 77.3Tergitol .TM. 0.82 78.6______________________________________
Examples and Comparison Examples Group 10
This group illustrates the use of materials suitable for forming a lubricant and surface conditioner layer on treated surfaces in Stage 2, the primary cleaning stage. The process sequence used in all these examples, unless otherwise noted, is shown in Table 22.
TABLE 22______________________________________PROCESS CONDITIONS FOR GROUP 10 Spray Dwell Blow-Off Tempera-Stage Time, Time, Time, ture, .degree.Number Sec Sec Sec C. Comments______________________________________1 30 10 30 54.4 Aqueous H.sub.2 SO.sub.4 at pH = 2.02 60 10 30 Variable3 Not used4 30 10 30 32.2 "Contaminated" rinse.sup.15 30 0 0 22 .+-. 3 Tap water rinse6 90 0 30 22 .+-. 3 DI water rinse______________________________________ Footnote for Table 22 .sup.1 The "contaminated" rinse water, intended to simulate normal conditions of commercial operation as a result of dragout, contained 60 m of the Stage 2 composition in 6 liters of tap water, sometimes with pH adjustment as noted specifically below.
Cans after stage 6 as described above were dried in an oven for 5 min at 150.degree. C. Interior brightness of the dried treated cans was measured in the same manner as described in .sctn.7.2 above. External appearance of the dried treated cans was judged by visual examination of cans rotated individually on an opaque surface. A whole number rating scale of 0 (worst) to 5 (best) was used. Previously prepared standard cans representative of each rating number were used for comparison. Five cans from each set were examined and the average rating number of the 5 was reported as appearance. The water break forming tendency was evaluated in the same manner as described above in .sctn.7.1
In order to simulate commercial operations, in which substantial amounts of lubricating oils are carried into the Wash Stage 2 despite the use of an acidic prewash, lubricating oils were normally added to the Stage 2 compositions tested. Two types of lubricating oil mixes were used. The "Low Tramp" Type consisted of 30% by weight of DTI 5600-M3 and 70% by weight of DTI 5600-WB, while the "High Tramp" Type consisted of 1/3 by weight of DTI 5600-M3, 1/3 by weight of Atochem SDO-5L-54-N2J, and 1/3 by weight of Mobil 629. (The oils including the letters "DTI" in their designations above are commercially available from Diversified Technology Inc., San Antonio, Tex., U.S., and the Atochem oil noted is available from Elf Atochem North America, Cornwells Heights, Pa., U.S.) Also, in order to simulate commercial operations in which substantial amounts of aluminum accumulate in the Stage 2 compositions, the Al.sup.+3 concentration of the Stage 2 compositions was adjusted with sodium aluminate. 3.2 grams of sodium aluminate.1.5 H.sub.2 O in 6 liters of total Stage 2 composition=100 ppm of aluminum ions.
Sequesterants have been historically included in alkaline can cleaners to help avoid magnesium oxide build up and staining of the can surfaces. Both of these normally unwanted phenomena are associated with the strongly alkaline conditions necessary to clean the can surface well.
Screening Group 10.1
A Plackett-Burman approach as outlined in prior statistical literature was used. The input variables studied constituted the best approximation of the critical parameters necessary to consider when designing a product and process for this application. Table 23 below outlines the experimental design. PHOSPHOTERIC.RTM. TC-6 is reported by its
TABLE 23__________________________________________________________________________INPUT VARIABLES FOR GROUP 10.1Factor (+1) Setting (-1) Setting__________________________________________________________________________ME Concentration 0.004 Mol/l 0.001 Mol/lME:Phosphate ester ETHOX .RTM. 2684 PHOSPHOTERIC .RTM. TC-6Quaternary salt ETHOQUAD .RTM. T-13 ETHODUOQUAD .RTM. T-15Spray time 60 Seconds 20 SecondsStage 2 Temperature 49.degree. C. 32.degree. C.Sequesterant Sodium gluconate 70% SorbitolSequesterant concentration 0.00482 Mol/l 0.000482 Mol/lStage 2 pH 12.0 11.5Cleaner surfactant 2.5 mL of "Mix 1"/L noneContaminated rinse pH 4.0 10.0Stage 2 Al.sup.+3 conc 2000 ppm 200 ppmLubricant oil load 1.0 g/L 0.1 g/LLubricant oil type Low tramp High tramp__________________________________________________________________________ Note for Table 23 "Mix 1" is a solution in tap water of 24.3% of SURFONIC .TM. LF17 and 14.6% of IGEPAL .TM. CO630.
supplier, Mona Industries of Patterson, N.J., to have an "R" moiety according to chemical formula (II): ##STR5## where at least one of R.sup.1 and R.sup.3 is carboxyethyl or salt thereof and the other is carboxyethyl, salt thereof, or hydrogen, and R.sup.2 is coconut oil alkyl, in chemical formula (III): ##STR6## where u is 1 or 2, y=(4-u), and M is hydrogen or sodium cation, except that at least one M must be sodium cation. ETHODUOQUAD.RTM. T- 15 is reported by its supplier to have the chemical formula: ##STR7##
The output variables measured were water break, COF, interior brightness, and visual appearance. Tables 24 and 25 below summarize the results of this group of examples. Only confidence coefficients .gtoreq.80.0% are listed. The sign of the coefficient corresponds to whether the resultant property is maximized at the (+1) level (+ sign) or the (-1) level (minus sign). From the results in Tables 24 and 25, it is clear that the quaternary salt mobility enhancing additives are much better at preventing water breaks and achieve a lower COF value. In most applications this makes them preferable to the phosphate ester types, even though the latter produce slightly higher interior brightness and appearance ratings.
TABLE 24______________________________________INPUT-OUTPUT CORRELATIONS FOR GROUP 10.1 WITHPHOSPHATE ESTER MOBILITY ENHANCER ADDITIONSInput Correlation Coefficient for Output Variables:Variable WB COF IB App______________________________________ME Conc.Ester Type 94.1Spray Time 87.6 -80.2S2 Temp. -95.8Sequesterant 93.2 99.9 99.9 92.0Seq. Conc. 96.0 99.7 93.4Stage 2 pH 98.5 99.9Stage 2 Surf. -81.4 99.0CR pH 91.9 86.0S2 Al.sup.+3 Conc. 99.9 99.9 -80.0 -90.9S2 Oil Conc. -99.9 -99.3S2 Oil Type______________________________________ Average Value of Output Variable: WB COF IB App______________________________________ 22.1 0.853 233 2.1______________________________________ Keys to Abbreviations for Table 24 WB = Water Breaks; IB = Interior Brightness; App. = Appearance; ME = Mobility Enhancer; S2 = Stage 2; Temp. = Temperature; Seq. = Sequesterant Conc. = Concentration; Surf. = Surfactant.
TABLE 25______________________________________INPUT-OUTPUT CORRELATIONS FOR GROUP 10.1 WITHQUATERNARY SALT MOBILITY ENHANCERADDITIONSInput Correlation Coefficient for Output Variables:Variable WB COF IB App______________________________________ME Conc.QSalt TypeSpray Time 99.9S2 Temp. 98.1Sequesterant -99.9Seq. Conc.Stage 2 pH 98.9 99.9 -93.0Stage 2 Surf. 94.9 93.7 81.4CR pH -98.9 95.2S2 Al.sup.+3 Conc. 99.9 -99.9 99.4S2 Oil Conc. -87.5S2 Oil Type______________________________________ Average Value of Output Variable: WB COF IB App______________________________________ 31.6 0.800 245 2.8______________________________________ Keys to Abbreviations for Table 25 WB = Water Breaks; IB = Interior Brightness; App. = Appearance; ME = Mobility Enhancer; QSalt = Quaternary Salt; S2 = Stage 2; Temp. = Temperature; Seq. = Sequesterant; Conc. = Concentration; Surf. = Surfactant.
Group 10.2: Effect of Sequesterant Type and of Rinsing Conditions
For this group, the following factors were all held constant: The Stage 2 composition contained 1 g/L of sequesterant, 1.25 mL/L of "Mix 1"as defined in the notes for Table 23, 2.0 g/L of Low Tramp oil as described above, 2 parts per thousand of Al.sup.+3, and 1.5 g/L of ETHOQUAD.TM. T-13. The pH of the Stage 2 composition was either 12.0 or 11.4. The sequesterant compositions used are shown in Table 26.
TABLE 26______________________________________SEQUESTERANT COMPOSITIONS FOR GROUP 10.2Sequesterant Percent in Mixture of:Mixture Number Na Gluconate Citric Acid Tartaric Acid______________________________________1 100 0 02 0 100 03 0 0 1004 50 50 05 50 0 506 0 50 507 33.3 33.3 33.3______________________________________
The process conditions were as shown in Table 22; both "non-acid rinse" with a base of tap water and "acid rinse" with a base of tap water adjusted to pH 2 with sulfuric acid were used, in each case deliberately "contaminated" with Stage 2 composition as noted in connection with Table 22. The results are shown in Tables 27 and 28. The pH values shown in these Tables were adjusted with sodium hydroxide.
TABLE 27______________________________________RESULTS OF GROUP 10.2 WITH pH = 11.4 IN STAGE 2Seq. No. Rinse WB COF IB App______________________________________1 Non-acid 31.9 0.561 216 2.82 30.8 0.549 217 3.03 31.9 0.551 217 2.24 30.7 0.566 216 2.45 31.2 0.532 221 2.06 31.5 0.497 217 1.87 31.5 0.609 222 2.01 Acid 27.5 0.726 220 2.82 27.8 0.726 216 2.23 27.1 0.568 215 2.04 29.5 0.718 219 2.45 30 0.717 219 2.46 29.1 0.596 216 2.07 27.9 0.618 216 2.0______________________________________ Notes for Table 27 "Seq. No." refers to the mixtures of sequesterants defined and numbered i Table 26. The other abbreviated column headings have the same meanings as in earlier tables.
TABLE 28______________________________________RESULTS OF GROUP 10.2 WITH pH = 12.0 IN STAGE 2Seq. No. Rinse WB COF IB App______________________________________1 Non-acid 28.2 0.595 258 4.22 27.0 0.564 255 4.03 28.6 0.526 253 4.04 29.0 0.620 265 4.05 27.7 0.616 262 3.46 31.2 0.535 238 3.47 30.4 0.559 263 3.81 Acid 31.7 0.697 258 3.82 31.3 0.658 254 3.83 31.9 0.822 223 3.44 28.9 0.764 275 3.45 22.8 0.698 271 3.86 31.8 0.723 237 4.47 31.6 0.710 264 3.8______________________________________ Notes for Table 28 "Seq. No." refers to the mixtures of sequesterants defined and numbered i Table 26. The other abbreviated column headings have the same meanings as in earlier tables.
The results in Tables 27 and 28 indicate that the higher pH of the Stage 2 composition favored appearance and brightness while the lower pH favored mobility. Also, tartaric acid as the sole sequesterant resulted in poorer interior brightness under most conditions that favored this characteristic, and it was therefore omitted from the following set of experiments.
Group 10.3; Effect of pH and Temperature, Concentrations Of Mobility Enhancing Additive and Lubricant Oil, and Concentration and Type of Sequesterant in Stage 2 Composition
A statistically designed group of 49 combinations from the set of input variables shown in Table 29 was evaluated for the four output variables as in the earlier subgroups in this group. The combinations in this subgroup, in addition to the ingredients shown in Table 29, all contained 2000 ppm of Al.sup.+3 ions and 1.25 mL/L of surfactant "Mix 1"as defined in the Notes for Table 23. The six combinations of this group that were judged best overall and the results for the four output variables with these conditions are shown in Table 30.
TABLE 29______________________________________INPUT VARIABLE VALUE TABLE FOR GROUP 10.3Input Variableand Unit Therefor Values of Input Variable in Set Tested______________________________________T-13 (g/L) 1.0 1.25 1.5 1.75 2.0Sod Gluc (g/L) 0 0.25 0.5 0.75 1.0Citric Ac (g/L) 1.0 0.75 0.5 0.25 0Lube oil (g/L) 0 0.5 1.0 1.5 2.0Stage 2 pH 11.8 11.9 12.0 12.1 12.2Stage 2 .degree.C. 37.8 43.3 48.9 54.4 60.0______________________________________ Notes for Table 29 "T13" = ETHOQUAD T13/50; "Sod Gluc" = Sodium gluconate; "Citric Ac" = Citric acid; Lube oil was of the "Low Tramp" type as described above.
TABLE 30__________________________________________________________________________SIX COMPOSITIONS FROM GROUP 10.3 WITH BEST OVERALL RESULTS Values ofValues of Input Variables: Output Variables:ME Conc. Na Gl. C. Cit. A. C. Lube C. St2 pH St2 .degree.C. WB App. COF IB__________________________________________________________________________1.25 0.25 0.75 0.50 12.1 43.3 29.8 3.4 0.571 2521.25 0.25 0.75 1.50 12.1 43.3 30.4 3.6 0.603 2461.25 0.25 0.75 0.50 12.1 54.4 30.0 4.0 0.595 2521.25 0.25 0.75 1.50 12.1 54.4 30.7 3.2 0.580 2551.50 0.50 0.50 0.00 12.0 48.9 30.9 3.2 0.596 2421.50 0.50 0.50 2.00 12.0 48.9 28.4 3.6 0.575 249__________________________________________________________________________ Notes for Table 30 "ME Conc." = concentration of ETHOQUAD T13/50; "Na Gl. C." = concentratio of sodium gluconate; "Cit. A. C." = concentration of citric acid; "Lube C." = Lube oil concentration; "St2 pH" = pH value in the Stage 2 cleaning composition; "St2 .degree.C." = temperature of the Stage 2 cleaning composition during contact with the containers being cleaned; units for all the concentrations noted are given in Table 29. The column heading abbreviations for the output variables have the same meaning as in previous tables herein.

Number	Name	Date
3964936	Das	Jun 1976
4148670	Kelly	Apr 1979
4273592	Kelly	Jun 1981
4313769	Frelin et al.	Feb 1982
4370177	Frelin et al.	Jan 1983
4599116	King et al.	Jul 1986
4647314	Mullins et al.	Mar 1987
4741863	Yamamoto et al.	May 1988
4859351	Awad	Aug 1989
4921552	Sander et al.	May 1990
4944889	Awad	Jul 1990
5030323	Awad	Jul 1991
5061389	Reichgott	Oct 1991
5064500	Awad	Nov 1991
5080814	Awad	Jan 1992
5110494	Beck	May 1992
5139586	Das	Aug 1992
5200114	Beck	Apr 1993
5308401	Geke et al.	May 1994
5380468	Gober et al.	Jan 1995
5399285	Kanluen	Mar 1995

	Number	Date	Country
Parent	521219	May 1990
Parent	395620	Aug 1989

	Number	Date
Parent	143803	Oct 1993
Parent	109791	Sep 1993
Parent	910483	Jul 1992
Parent	785635	Oct 1991
Parent	57129	Jun 1987

Aqueous lubricant and surface conditioner for formed metal surfaces

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