Stability of detergents containing hypochlorite, phosphonate chelant, and optical brightener

Information

  • Patent Grant
  • 7786066
  • Patent Number
    7,786,066
  • Date Filed
    Thursday, June 26, 2008
    16 years ago
  • Date Issued
    Tuesday, August 31, 2010
    14 years ago
Abstract
The stability of aqueous, liquid detergents containing hypochlorite and brighteners is achieved by the use of a specific complexing agent.
Description
STATEMENT REGARDING FEDERALLY SPONSORED RESEARCH OR DEVELOPMENT

Not Applicable


INCORPORATION-BY-REFERENCE OF MATERIAL SUBMITTED ON A COMPACT DISC

Not Applicable


BACKGROUND OF THE INVENTION

(1) Field of the Invention


The present invention relates to the stabilization of hypochlorite-containing liquid laundry detergents which contain optical brighteners.


Sodium hypochlorite is known as a highly effective bleaching agent and has long been used, optionally together with soaps and/or synthetic surfactants, for removing stains and all kinds of soiling, not only when laundering textiles but also when cleaning hard surfaces. It is usually sold for household use in concentrations of approx. 2 wt. % to 10 wt. % in water.


Liquid laundry detergent preparations or corresponding preparations of cleaning agents for hard surfaces which contain hypochlorite as bleaching component are susceptible, when stored for an extended period, to suffering a loss in activity, in particular, due to the hypochlorite degradation which occurs in such cases. Constituents which are desired in laundry detergents and cleaning agents from an applicational standpoint or for aesthetic reasons also include, in addition to the active ingredients which decisively influence performance, among which hypochlorite may, in particular, be mentioned, those active ingredients which tend more to have an impact on the optical appearance of the textiles treated therewith. These, in particular, include optical brighteners which become attached to the fibers of the textile material during the washing operation. These compounds are capable of absorbing light and emitting shorter wavelength light. The overall result of absorbing red and yellow colored light and emitting blue to ultraviolet light is an increase in the intensity of light perceived as white, such that a textile treated in this manner appears optically brighter. For white laundry, this is a very desirable effect; laundry detergents which are intended to be used for washing colored textiles generally contain no optical brighteners. Optical brighteners are highly susceptible to oxidative attack by hypochlorite, which means that, after storage, corresponding agents containing both of these components, in addition to the consequent loss of bleaching agent, also exhibit the disadvantage that the active ingredient of the optical brightener which is jointly responsible for the optical impression of whiteness is no longer available, or at least not in its entirety.


(2) Description of Related Art, Including Information Disclosed Under 37 C.F.R. Sections 1.97 and 1.98


International Patent Application WO 99/15616 proposes adding free-radical scavengers to hypohalite-containing bleaching agents which contain optical brighteners in order to stabilize the optical brighteners.


BRIEF SUMMARY OF THE INVENTION

It has surprisingly now been found that certain compounds, which are not free-radical scavengers, make a highly effective contribution to stabilizing optical brighteners in hypochlorite-containing liquids.


The present invention provides the use of diethylenetriaminepentamethylene-phosphonic acid and/or the alkali metal salt thereof for stabilizing optical brighteners in aqueous liquid laundry detergents which contain alkali metal hypochlorite.


It has surprisingly now been found that when diethylenetriaminepentamethylene-phosphonic acid and/or the alkali metal salts thereof are added to hypochlorite-containing liquid agents, the stability of optical brighteners contained in these agents is increased and also the hypochlorite is less rapidly degraded during storage than is the case without said addition.


The present invention secondly provides an aqueous liquid bleaching agent or bleaching laundry detergent containing alkali metal hypochlorite and optical brightener, which is characterized in that it additionally contains diethylenetriaminepentamethylenephosphonic acid and/or the alkali metal salt thereof.


BRIEF DESCRIPTION OF THE SEVERAL VIEWS OF THE DRAWING(S)

Not Applicable







DETAILED DESCRIPTION OF THE INVENTION

It is normally sufficient for the liquid agent to be stabilized to contain more than 0 wt. % up to approx. 1 wt. %, in particular approx. 0.01 wt. % to approx. 0.5 wt. % of diethylenetriamine-pentamethylenephosphonic acid and/or the alkali metal salt thereof. Diethylenetriaminepentamethylenephosphonic acid is commercially obtainable, for example, under the trade name Dequest® 2066.


The agent according to the invention may contain any desired alkali metal salts of diethylenetriaminepentamethylenephosphonic acid. It is preferred to use the mono-, di-, tri-, tetra- or penta-sodium salt, which may be introduced as such in the course of producing agents according to the invention or is formed in situ from the free diethylenetriaminepentamethylene-phosphonic acid which is introduced instead, and alkali metal.


The optical brightener stabilized according to the invention is preferably selected from a compound according to one of the following formulae (I) to (VIII) or mixtures thereof, it being possible for those compounds shown with a C═C double bond in trans configuration also to be present at least in part with said bond in cis configuration:




embedded image


embedded image


In these formulae

  • R1 means hydrogen, —SO3M, —OR13, —CN, —Cl, —COOR13, —CON(R13)2
  • R2 and R3 mutually independently mean hydrogen, —R13 or —Ar,
  • R4 and R5 mutually independently mean —OH, —Cl, —NH2, —OR13, —O—Ar, —NHR13, —N(R13)2, —NR13R14, —N(R14)2, —NH—Ar, a morpholino group, —S—R13 or —S—Ar,
  • R6 means hydrogen, —Cl or —SO3M,
  • R7 means —CN, —SO3M, —S—R13 or —S—Ar,
  • R8 means hydrogen, —R13, —Cl or —SO3M,
  • R9 and R10 mutually independently mean hydrogen, —R13, —Cl, —SO3M or —OR13,
  • R11 means hydrogen or —R13,
  • R12 means hydrogen, —R13, —CN, Cl, —COOR13, —CO N(R13)2, —Ar or —O—Ar,
  • R13 means a branched or unbranched C1 to C4 alkyl group
  • R14 means a branched or unbranched C1 to C4 hydroxyalkyl group,
  • Ar means a phenyl, naphthyl, pyrindinyl, pyridazinyl, pyrimidinyl, pyrazinyl, triazinyl, indolyl, anthracenyl, phenanthrenyl or benzonaphthyl group optionally substituted with —R13, —Cl, —SO3M or —OR13,
  • M means hydrogen, Na, K, Ca, Mg, ammonium, mono-, di-, tri- or tetra-R13-substituted ammonium, mono-, di-, tri- or tetra-R14-substituted ammonium or ammonium mono-, di-, tri- or tetra-substituted with a mixture of R13 and R14.


Optical brighteners which correspond to the formulae (I) or (II) are particularly preferably used. For example, the compound according to formula (I) with R1=M=H is obtainable under the name Tinopal® CBS-X from Ciba-Geigy and the compound according to formula (II) with R2=M=H, R3=phenyl is obtainable under the name Optiblanc® BRB from 3V Sigma. Laundry detergents or bleaching agents conventionally contain only small quantities of optical brighteners, for example from 10 ppm to 0.5 wt. %.


Preparations according to the invention are, in particular, suitable and highly effective as a bleaching agent or bleaching laundry detergent for white textiles. An agent according to the invention is active against a plurality of stains, including fatty soiling such as sebum, makeup or lipstick, enzymatically removable soiling such as blood, grass or cocoa, and bleachable soiling such as wine, coffee or tea, even after the composition has aged, i.e., if it has been stored for an extended period after manufacture.


A further advantage of bleaching agents according to the present invention is that they are suitable for bleaching textiles made from various materials, including those made from natural fibers such as cotton or linen, as well as those made from synthetic material, such as synthetic polymer fibers, and also those made from corresponding blend fabrics.


A liquid agent according to the present invention is advantageously applied onto the textiles to be cleaned in diluted form, for example, if it is used as a washing additive in hand or machine washing of textiles, or alone as a laundry detergent, but it may additionally or alternatively also be applied undiluted onto the textile, for example, as a liquid pretreatment agent or stain remover.


A bleaching agent in the form of hypochlorite is an essential constituent of the agents according to the invention. Bleaching agents per se are entirely known components of laundry detergent and cleaning agent compositions and are, in particular, also successful in combating mildew and mold and in disinfection. Although other alkali metal hypochlorites, such as, for example, potassium hypochlorite, are usable, it is nevertheless preferred to use sodium hypochlorite in agents stabilized according to the invention. Conventional commercial aqueous sodium hypochlorite solutions often contain considerable quantities of chloride salts. These may straightforwardly be used for producing agents according to the invention, such that it is not necessarily essential to use high purity NaOCl. In a preferred embodiment of the invention, the agents contain 0.5 wt. % to 5 wt. %, in particular, 1 wt. % to 4 wt. %, of alkali metal hypochlorite.


The agents stabilized according to the invention are usually alkaline and may for this purpose contain approx. 0.1 wt. % to 2 wt. %, in particular, 0.1 wt. % to 1.1 wt. %, of alkali metal hydroxide. The preferred alkali metal hydroxide is sodium hydroxide and the alkali metal salts which are mentioned in connection with the other constituents of the agent are likewise preferably sodium salts.


The preparations may contain surfactants which are stable in the presence of hypochlorite. Betaines are preferred, in particular those of the general formula IX,




embedded image



in which R14 is an alkyl or alkenyl group having 6 to 22 carbon atoms or a group R17CO—NH—(CH2)n—, R15 is hydrogen or an alkyl group having 1 to 4 carbon atoms, R16 is hydrogen or an alkyl group having 1 to 4 carbon atoms, R17 is an alkyl or alkenyl group having 6 to 22 carbon atoms, m is a number from 1 to 6 and n is a number from 1 to 3. Examples of particularly suitable representatives of this class of surfactants include C12-18-alkyldimethylbetaine, commercially obtainable as coconut betaine, and C10-16-alkyldimethylbetaine, commercially obtainable as lauryl betaine. A further class of particularly preferred surfactants are alkyl ether sulfates, which are obtainable by reacting alcohols (preferably having 6 to 22 carbon atoms) with alkylene oxides, in particular, ethylene oxide, and subsequent sulfation and neutralization, in particular, a C12-14 fatty alcohol ether sulfate alkoxylated with 2 equivalents of ethylene oxide. The corresponding cation in the ether sulfates is preferably sodium. Surfactants are preferably present in agents stabilized according to the invention in quantities of up to 20 wt. %, in particular, of 0.1 wt. % to 15 wt. %.


In addition to the diethylenetriaminepentamethylenephosphonic acid and/or the alkali metal salt thereof, the preparations may optionally contain further sequestrants, preferably alkylphosphonic acids having at least one amine oxide substituent on the alkyl group, here designated amine oxide phosphonic acids, polyacrylic acids and/or polyacrylic acids comprising phosphono groups, which may also be present in the form of the alkali metal salts thereof. Incorporating such complexing agents surprisingly gives rise to particularly good stability of the hypochlorite. Amine oxide phosphonic acids are usually produced by oxidation of aminoalkylphosphonic acids. They preferably belong to the group of compounds of the general formula (X),




embedded image



in which R13 is hydrogen, a —(CH2)x(CHCH3)y—NH2->O group or an alkali metal, x is a number from 1 to 4 and y is 0 or 1. The amine oxide based on aminotrimethylenephosphonic acid is among the particularly preferred amine oxide phosphonic acids. Such additional sequestrants are preferably present in an amount of 0.01 wt. % to 2 wt. %.


In addition to the stated constituents, the preparations stabilized according to the invention may contain small quantities of pH-buffering substances and/or one or more bleach-stable dyes or odoriferous substances. The optionally present fragrance component is preferably of a higher relative volatility than the constituents which are responsible for any bleach odor. The agents preferably contain more than 0 wt. % to approx. 0.01 wt. %, in particular, approx. 0.001 wt. % to approx. 0.008 wt. % of a colored, in particular, blue and/or green, metal pigment. Among these, complex compounds of nickel, cobalt, copper, iron and/or manganese are preferred; copper phthalocyanine dyes are particularly preferred. The stability both of the colored metal pigment and also of the alkali metal hypochlorite is increased by the presence of alkali metal iodide. Therefore, agents according to the invention preferably contain more than 0 wt. % up to approx. 0.01 wt. %, in particular approx. 0.001 wt. % to approx. 0.006 wt. % of alkali metal iodide, in particular potassium iodide. Usable pH-buffering constituents are preferably selected from among carbonates, polycarbonates, sesquicarbonates, silicates, polysilicates, borates, phosphates, stannates, aluminates of alkali metals and mixtures of these, with preferred alkali metals being sodium and potassium. Starting materials for producing, for example, the hypohalite bleaching agent may contain secondary products, for example, carbonate, which may give rise to a content of such secondary products of optionally up to 0.4 wt. % in agents according to the invention.


The aqueous compositions according to the invention usually have viscosities in the range from approx. 25 mPa·s to 1500 mPa·s, in particular, from 50 mPa·s to 1100 mPa·s.


A composition according to the invention may, in diluted or undiluted form, be used for removing soiling and stains from textiles by bringing the composition and the textile into contact with one another for a period which is sufficient for bleaching of the textile, and thereafter rinsing the textile with water. Alternatively thereto or alternatively to rinsing with water, the textile may also be washed using an agent according to the invention by hand or in machine washing process in which an agent according to the invention is dispensed into a conventional washing machine.


EXAMPLE

In an aqueous composition containing 1.43 mmol/l of NaOCl, 8.10−4 mmol/l of Tinopal® CBS-X and 0.36 mmol/l of Dequest® 2066, the decrease in fluorescence of the optical brightener after storage for 1 hour amounted to 16%, whereas it amounted to 94% in an otherwise identical composition which did not contain the diethylenetriaminepentamethylene-phosphonic acid and was stored under identical conditions.


If the stated optical brightener was replaced with 1.5·10−4 mmol/l of Hostalux® PCNX, the decreases amounted to 16% and 71%.


If the stated optical brightener was replaced with 7.5·10−4 mmol/l of Optiblanc® BRB and 0.018 mmol/l of Fe was additionally added to the solutions, the decreases amounted to 4% and 97%.

Claims
  • 1. An aqueous laundry detergent comprising: a) diethylenetriaminepentamethylenephosphonic acid and/or the alkali metal salt thereof;b) an optical brightener of the formula:
  • 2. The composition of claim 1 wherein the alkali metal salt is a sodium salt.
  • 3. The composition of claim 1 wherein the composition contains from 0.01 wt. % to 1.0 wt. % of diethylenetriaminepentamethylenephosphonic acid and/or the alkali metal salt thereof.
  • 4. The composition of claim 1 wherein the amount of the diethylenetriaminepentamethylenephosphonic acid and/or the alkali metal salt thereof is from 0.01 wt. % to 0.5 wt. %.
  • 5. The composition of claim 1 further comprising an additional optical brightener selected from the group consisting of a compound of the formulae (I) to (VIII) or mixtures thereof
  • 6. The composition of claim 1 wherein the amount of alkali metal hypochlorite is from 0.5 wt. % to 5 wt. %.
  • 7. The composition of claim 1 wherein the alkali metal hypochlorite is sodium hypochlorite.
  • 8. The composition of claim 1 wherein the amount of the optical brightener is from 10 ppm to 0.5 wt. %.
  • 9. A method for stabilizing an optical brightener in an aqueous liquid laundry detergent comprising: adding less than about 1.0 wt. % ofa) diethylenetriaminepentamethylenephosphonic acid and/or the alkali metal salt thereof to the aqueous liquid laundry detergent, which further comprises;b) an optical brightener of the formula:
  • 10. The method of claim 9 further comprising an additional optical brightener selected from the group consisting of a compound of the formulae (I) to (VIII) or mixtures thereof
  • 11. The method of claim 1 wherein the amount of the optical brightener is from 10 ppm to 0.5 wt. %.
Priority Claims (1)
Number Date Country Kind
10 2005 063 177 Dec 2005 DE national
CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation under 35 U.S.C. Section 365(c) and 35 U.S.C. Section 120 of International Application No. PCT/EP2006/011814, filed Dec. 8, 2006. This application also claims priority under 35 U.S.C. Section 119 of German Patent Application No. DE 10 2005 063177.0, filed Dec. 30, 2005. Both the International Application and the German Application are incorporated herein by reference in their entireties.

US Referenced Citations (25)
Number Name Date Kind
3393153 Zimmerer et al. Jul 1968 A
3655566 Robinson et al. Apr 1972 A
3666680 Briggs May 1972 A
3876551 Laufer et al. Apr 1975 A
4113645 DeSimone Sep 1978 A
4116849 Leikhim Sep 1978 A
4193888 McHugh Mar 1980 A
4411799 Ito et al. Oct 1983 A
4828723 Cao et al. May 1989 A
4830782 Broze et al. May 1989 A
5139695 Eckhardt Aug 1992 A
5180514 Farr et al. Jan 1993 A
5185096 Ahmed Feb 1993 A
5229027 Ahmed Jul 1993 A
5972038 Amestica et al. Oct 1999 A
6083892 Severns et al. Jul 2000 A
6090770 Mendoza et al. Jul 2000 A
6204235 Jimenez et al. Mar 2001 B1
6448215 Grande et al. Sep 2002 B1
6506718 Todini Jan 2003 B1
6649583 Todini Nov 2003 B2
6894015 Briatore et al. May 2005 B1
20030032565 Sivik Feb 2003 A1
20040023837 Zanardi Feb 2004 A1
20040192576 Schmid et al. Sep 2004 A1
Foreign Referenced Citations (41)
Number Date Country
2810187 Sep 1978 DE
3201460 Aug 1982 DE
4140830 Jun 1992 DE
19700799 Jul 1998 DE
19803054 Jul 1999 DE
19855329 Jun 2000 DE
102004020017 Nov 2005 DE
0079102 May 1983 EP
311175 Apr 1989 EP
0351947 Jan 1990 EP
439878 Aug 1991 EP
0462793 Dec 1991 EP
0565788 Oct 1993 EP
0606707 Jul 1994 EP
0622451 Nov 1994 EP
0812909 Dec 1997 EP
0867503 Sep 1998 EP
0903403 Mar 1999 EP
905223 Mar 1999 EP
0905225 Mar 1999 EP
931829 Jul 1999 EP
1001010 May 2000 EP
1348755 Jan 2003 EP
1391501 Feb 2004 EP
1462512 Sep 2004 EP
1462564 Sep 2004 EP
1614742 Jan 2006 EP
2271119 Apr 1994 GB
52069415 Jun 1977 JP
07233396 Sep 1995 JP
WO9305136 Mar 1993 WO
WO9407987 Apr 1994 WO
WO9410280 May 1994 WO
WO9706233 Feb 1997 WO
WO9745523 Dec 1997 WO
WO9915616 Apr 1999 WO
WO9928427 Jun 1999 WO
WO2004085590 Oct 2004 WO
WO2004104157 Dec 2004 WO
WO2006010089 Jan 2006 WO
WO2006048104 May 2006 WO
Related Publications (1)
Number Date Country
20080305980 A1 Dec 2008 US
Continuations (1)
Number Date Country
Parent PCT/EP2006/011814 Dec 2006 US
Child 12147405 US