Patent Application
20210189290
The present invention concerns the field of alkoxylated phenol derivatives. These inventive compounds may advantageously be used as anti-redeposition agents in washing applications.
Anti-redeposition agents used in laundry detergents help to prevent soil from resettling on a fabric after it has been removed during washing. This can for example be achieved by dispersing the soil in the washing liquor.
The washing of soiled fabrics with a laundry detergent composition is essentially a two-step process. In the first stage the detergent must remove the soil from the fabric and suspend it in the washing liquor. In the second stage the detergent composition must prevent the soil and other insoluble materials from re-depositing on the cloth before the fabric is removed from the washing liquor or the rinse liquor. Polymers are known to aid both processes. For example, soil release polymers enhance soil removal from the fabric whilst anti-redeposition polymers prevent the removed soil from re-depositing on the fabric.
Examples of suitable anti-redeposition agents include fatty acid amides, fluorocarbon surfactants, complex phosphate esters, styrene maleic anhydride copolymers, and cellulosic derivatives such as hydroxyethyl cellulose, hydroxypropyl cellulose, and the like.
U.S. Pat. No. 4,240,918 e.g. describes polymers having anti-soiling and anti-redeposition properties, for example hydrophilic polyurethanes, certain copolyesters and mixtures thereof.
However, many of the known anti-redeposition agents possess the disadvantage that their performance and whitening effect in washing or laundry applications are insufficient.
Therefore, the problem to be solved by the present invention is to provide new anti-redeposition agents that have favourable performance and lead to enhanced “whiteness” when used in washing or laundry applications.
Surprisingly it has been found that this problem can be solved by alkoxylates obtainable by
Therefore, the subject matter of the present invention is alkoxylates obtainable by
Suitable alkylating agents providing C1-C4 alkyl groups are e.g. dialkylsulfates with C1-C4 alkyl groups and preferably dimethylsulfate, C1-C4 alkylhalogenides, preferably C1-C4 alkylchlorides, -bromides or -iodides and more preferably C1-C4 alkylchlorides, C1-C4 alkyltosylates or C1-C4 alkylmesylates.
Suitable carboxymethylating agents are e.g. chloroacetic acid, bromoacetic acid, iodoacetic acid or their salts and preferably chloroacetic acid.
Suitable sulfating agents are e.g. SO3 or amidosulfonic acid.
Suitable phosphating agents are e.g. polyphosphoric acid, phosphorous oxides such as P2O5, PCl3 in combination with an oxidation reaction and PCl5 or POCl3 in combination with a hydrolysis.
Suitable sulfosuccinating agents are e.g. maleic anhydride in combination with sulfite.
Reactions of a compound comprising an OH group with an alkylating agent providing a C1-C4 alkyl group, with a carboxymethylating agent, with a sulfating agent, with a phosphating agent or with a sulfosuccinating agent are already known. Reactions of this kind are e.g. described in WO 2008/138486 A1.
The inventive alkoxylates exhibit favourable performance as anti-redeposition agents in washing or laundry applications. They exhibit favourable performance as dispersants and in washing or laundry applications they lead to enhanced “whiteness”. Furthermore, the inventive alkoxylates exhibit favourable stability and in particular favourable hydrolytic stability. Inventive alkoxylates furthermore enhance stain removal and lead to enhanced cleaning. Preferably, inventive alkoxylates furthermore exhibit favourable biodegradability.
In step (i) an “aryl-substituted linear or branched C1-C3 alkyl alcohol” or an “aryl-substituted linear or branched C2- or C3-alkene” is reacted.
The “aryl-substituted linear or branched C1 to C3 alkyl alcohol” denotes a linear or branched C1 to C3 alkyl alcohol which is substituted by an aryl group. The aryl group in these reactants preferably comprises 6 to 10 carbon atoms. More preferably, the “aryl-substituted linear or branched C1 to C3 alkyl alcohol” is benzyl alcohol.
The “aryl-substituted linear or branched C2- or C3-alkene” denotes a linear or branched C2- or C3-alkene which is substituted by an aryl group. The aryl group in these reactants preferably comprises 6 to 10 carbon atoms. More preferably, the “aryl-substituted linear or branched C2- or C3-alkene” is styrene or alpha-methylstyrene and even more preferably is styrene.
Tristyrylphenol ethoxylates are known compounds that are for example described in US 2008/0255204 A1 or WO 99/40784 A1.
Tristyrylphenol ethoxylates comprising compounds of the following structure (II)
are commercially available from different sources, e.g. Clariant. Examples for products are Emulsogen® TS 160 (g=16, meaning a molecular average of 16 mol EO per mol of phenol, “EO” meaning ethylene oxide) and Emulsogen® TS 540 (g=54, meaning a molecular average of 54 mol EO per mol of phenol).
Ethoxylated and styrenated phenol derivatives are for example also described in US 2003/0196685 A1.
Preferably, the inventive alkoxylates are obtainable in that the molar ratio of the aryl-substituted linear or branched C1-C3 alkyl alcohols or the aryl-substituted linear or branched C2- or C3-alkenes mentioned under b) of the first step, preferably the aryl-substituted linear or branched C2- or C3-alkenes, more preferably styrene or alpha-methylstyrene and even more preferably styrene, to the one or more compounds selected from the group consisting of the substituted phenols mentioned under a) of the first step is of from 1:1 to 3:1, preferably of from 2:1 to 3:1 and more preferably is 2:1.
Furthermore preferably, the inventive alkoxylates are obtainable in that the molar ratio of alkoxylation agent to the one or more compounds selected from the group consisting of the substituted phenols mentioned under a) of the first step is of from 5:1 to 100:1, preferably of from 7:1 to 80:1, more preferably of from 8:1 to 70:1, even more preferably of from 9:1 to 60:1 and particularly preferably of from 10:1 to 35:1.
Furthermore preferably, the inventive alkoxylates are obtainable in that the one or more compounds selected from the group consisting of the substituted phenols mentioned under a) of the first step are selected from the group consisting of ortho-dihydroxybenzene, meta-dihydroxybenzene, para-dihydroxybenzene, ortho-methoxyphenol, meta-methoxyphenol and para-methoxyphenol, more preferably are selected from the group consisting of ortho-methoxyphenol and para-methoxyphenol and even more preferably the compound is para-methoxyphenol.
Furthermore preferably, the inventive alkoxylates are obtainable in that the alkoxylation of the second step is an ethoxylation or a combination of both an ethoxylation and a propoxylation and preferably an ethoxylation.
More preferably, the inventive alkoxylates are obtainable in that the alkoxylation of the second step is a reaction with ethylene oxide or with ethylene oxide and propylene oxide, in this case preferably with more ethylene oxide than propylene oxide and in this case furthermore preferably either simultaneously or successively, and particularly preferably the alkoxylation of the second step is a reaction with only ethylene oxide.
Preferably, the inventive alkoxylates are obtainable in that both steps (i) and (ii) are performed in the presence of a catalyst.
More preferably, the inventive alkoxylates are obtainable in that the catalyst of step (i) is an acid, preferably a Broensted acid and the catalyst of step (ii) is a base or a double metal cyanide catalyst, preferably a base selected from the group consisting of alkali methoxide or alkali hydroxide, more preferably selected from the group consisting of NaOH, KOH, NaOCH3 and KOCH3, even more preferably selected from the group consisting of NaOCH3 and KOCH3 and particularly preferably NaOCH3.
Preferably, the inventive alkoxylates are obtainable in that the reactions of steps (i) and (ii) are performed in the absence of solvent.
Furthermore preferably, the inventive alkoxylates are obtainable in that the reaction of step (i) is performed at a temperature of from 100 to 180° C. and preferably of from 120 to 150° C. and the reaction of step (ii) is performed at a temperature of from 75 to 220° C., preferably of from 100 to 200° C. and more preferably of from 130 to 150° C.
Furthermore preferably, the inventive alkoxylates are obtainable in that the reaction of step (i) is performed at ambient pressure and the reaction of step (ii) is performed at a pressure of from 1 to 100 bar and preferably of from 2 to 10 bar.
In one preferred embodiment of the invention the inventive alkoxylates are obtainable by not performing step (iii).
In another preferred embodiment of the invention the inventive alkoxylates are obtainable by performing step (iii).
In a particularly preferred embodiment of the invention, the inventive alkoxylates are obtainable by
A subject matter of the invention solving the problem posed is also alkoxylates according to the following formula (I)
wherein
X is selected from ethoxy and mixtures of ethoxy and propoxy groups, preferably is selected from ethoxy and mixtures of ethoxy and propoxy groups where the number of ethoxy groups in the mixtures is greater than the number of propoxy groups and more preferably X is ethoxy,
T is selected from the group consisting of H, C1-C4 alkyl, SO3−, CH2—COO−, sulfosuccinate and PO32−, preferably is selected from the group consisting of H and CH3 and more preferably is H,
R3-R7 are independently of one another H, Y, aryl, aryl-substituted linear or branched C1 to C3 alkyl or O(Z)mT1, preferably H, Y, aryl-substituted linear or branched C1 to C3 alkyl or O(Z)mT1, the aryl-substituted linear or branched C1 to C3 alkyl preferably is selected from the group consisting of C6H5CHCH3 and C6H5C(CH3)2 and more preferably the aryl-substituted linear or branched C1 to C3 alkyl is C6H5CHCH3,
Y is R8, OR8, F, Cl, Br, I, CN, NO2 or COOR9, wherein R8 is a linear or branched alkyl group with 1 to 4 C-atoms and R9 is a linear or branched alkyl group comprising 1 to 22 C-atoms or a linear or branched mono- or polyunsaturated alkenyl group comprising 2 to 22 C-atoms, preferably R9 is a linear or branched alkyl group comprising 1 to 18 C-atoms or a linear or branched mono- or polyunsaturated alkenyl group comprising 2 to 18 C-atoms and more preferably R9 is a linear or branched alkyl group comprising 1 to 4 carbon atoms, and preferably Y is CH3, C2H5, OCH3, OC2H5, Cl, CN, NO2 or COOR9, more preferably CH3, OCH3, Cl, CN or COOR9, even more preferably CH3, OCH3 or COOR9 and particularly preferably OCH3,
Z is selected from ethoxy and mixtures of ethoxy and propoxy groups, preferably ethoxy and mixtures of ethoxy and propoxy groups where the number of ethoxy groups in the mixtures is greater than the number of propoxy groups and more preferably Z is ethoxy,
T1 is selected from the group consisting of H, C1-C4 alkyl, SO3−, CH2—COO−, sulfosuccinate and PO32−, preferably is selected from the group consisting of H and CH3 and more preferably is H,
n+m on a molar average is a number of from 5 to 100, preferably of from 7 to 80, more preferably of from 8 to 70, even more preferably of from 9 to 60 and particularly preferably of from 10 to 35,
characterised in that exactly one of the substituents R3-R7 is O(Z)mT1 or Y, preferably Y, and one to three, preferably two or three of the other substituents R3-R7 are aryl or aryl-substituted linear or branched C1 to C3 alkyl, preferably aryl-substituted linear or branched C1 to C3 alkyl, more preferably selected from the group consisting of C6H5CHCH3 and C6H5C(CH3)2 and even more preferably C6H5CHCH3.
In a preferred embodiment of the invention, inventive alkoxylates according to formula (I) are obtainable by performing the above-mentioned steps (i) and (ii) and optionally also the above-mentioned step (iii).
In the inventive alkoxylates according to formula (I) exactly one of the substituents R3-R7 is “O(Z)mT1” or “Y”. This e.g. means that in the inventive alkoxylates according to formula (I) none of the substituents R3-R7 can have the meaning “O(Z)mT1” in case one of these substituents is “Y” and none of the substituents R3-R7 can have the meaning “Y” in case one of these substituents is “O(Z)mT1”.
In case T and/or T1 are selected from the group consisting of SO3−, CH2—COO−, sulfosuccinate and PO32− the inventive alkoxylates comprise a counter cation. This counter cation is preferably selected from the group consisting of alkali metal ions, alkaline earth metal ions and NH4+, more preferably from the group consisting of Na+ and NH4+.
In formula (I), the substituents R3-R7 may have the meaning “aryl”. Preferably, the substituent “aryl” comprises 6 to 10 carbon atoms and more preferably, the substituent “aryl” is phenyl.
In formula (I), the substituent “aryl-substituted linear or branched C1 to C3 alkyl” denotes a linear or branched C1 to C3 alkyl group which is substituted by an aryl group. The “aryl” preferably comprises 6 to 10 carbon atoms. More preferably, the substituent “aryl-substituted linear or branched C1 to C3 alkyl” is selected from the group consisting of C6H5CHCH3 and C6H5C(CH3)2 and even more preferably is C6H5CHCH3.
Preferably, the inventive alkoxylates are selected from the compounds according to formula (I) wherein
X is selected from ethoxy and mixtures of ethoxy and propoxy groups, preferably is selected from ethoxy and mixtures of ethoxy and propoxy groups where the number of ethoxy groups in the mixtures is greater than the number of propoxy groups and more preferably X is ethoxy,
T is H,
R3-R7 are independently of one another H, OCH3, C6H5CHCH3 or O(Z)mH,
Z is selected from ethoxy and mixtures of ethoxy and propoxy groups, preferably ethoxy and mixtures of ethoxy and propoxy groups where the number of ethoxy groups in the mixtures is greater than the number of propoxy groups and more preferably Z is ethoxy,
n+m on a molar average is a number of from 5 to 100, preferably of from 7 to 80, more preferably of from 8 to 70, even more preferably of from 9 to 60 and particularly preferably of from 10 to 35,
characterised in that exactly one of the substituents R3-R7 is O(Z)mH or OCH3, preferably OCH3, and one to three of the other substituents R3-R7 are C6H5CHCH3 and preferably two or three of the other substituents R3-R7 are C6H5CHCH3.
The substituent “C6H5CHCH3” has the structure
the substituent “C6H5C(CH3)2” has the structure
“sulfosuccinate” has the structure
“ethoxy” or “ethyleneoxy” has the structure
—CH2CH2O— and
“propoxy” or “propyleneoxy” has the structure
In a preferred embodiment of the invention the sum “n+m” in the inventive alkoxylates according to formula (I), on a molar average, is 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31 or 32.
In the inventive alkoxylates according to formula (I) the sum “n+m”, on a molar average, is a number of from 5 to 100, preferably of from 7 to 80, more preferably of from 8 to 70, even more preferably of from 9 to 60 and particularly preferably of from 10 to 35 and n and m, on a molar average and independently of one another, preferably are numbers of from 0 to 100, more preferably of from 0 to 80, even more preferably of from 0 to 70, particularly preferably of from 0 to 60 and extraordinarily preferably of from 0 to 35.
In one preferred embodiment of the invention one of the substituents R3-R7 in the inventive alkoxylates according to formula (I) is Y and more preferably OCH3. Therefore, in the inventive alkoxylates according to formula (I) of this preferred embodiment of the invention none of the substituents R3-R7 can have the meaning O(Z)mT1. In this preferred embodiment of the invention n, on a molar average, is a number of from 5 to 100, preferably of from 7 to 80, more preferably of from 8 to 70, even more preferably of from 9 to 60 and particularly preferably of from 10 to 35.
In another preferred embodiment of the invention one of the substituents R3-R7 in the inventive alkoxylates according to formula (I) is O(Z)mT1 and more preferably O(Z)mH. Therefore, in the inventive alkoxylates according to formula (I) of this preferred embodiment of the invention none of the substituents R3-R7 can have the meaning Y. In this preferred embodiment of the invention n and m, on a molar average and independently of one another, preferably are numbers of from 1 to 75, more preferably of from 2 to 60, even more preferably of from 3 to 50, particularly preferably of from 4 to 40 and extraordinarily preferably of from 5 to 25.
In another preferred embodiment of the invention two of the substituents R3-R7 in the inventive alkoxylates according to formula (I) are aryl or aryl-substituted linear or branched C1 to C3 alkyl, preferably aryl-substituted linear or branched C1 to C3 alkyl, more preferably selected from the group consisting of C6H5CHCH3 and C6H5C(CH3)2 and even more preferably C6H5CHCH3, and more preferably these two substituents are in the ortho-positions to the group O—[X]n-T.
In a particularly preferred embodiment of the invention in the inventive alkoxylates according to formula (I) X is ethoxy, T is H, R4 is O(Z)mH, Z is ethoxy, n+m, on a molar average, is a number of from 5 to 35, one of the substituents R3, R5, R6 and R7 is H and the other three of these substituents are C6H5CHCH3, and preferably, n and m, on a molar average and independently of one another, are numbers of from 2 to 20.
In a further particularly preferred embodiment of the invention in the inventive alkoxylates according to formula (I) X is ethoxy, T is H, R3 is O(Z)mH, Z is ethoxy, n+m, on a molar average, is a number of from 5 to 35, two of the substituents R4, R5, R6 and R7 are H and the other two of these substituents are C6H5CHCH3, and preferably, n and m, on a molar average and independently of one another, are numbers of from 2 to 20.
In a further particularly preferred embodiment of the invention in the inventive alkoxylates according to formula (I) X is ethoxy, T is H, R4 is O(Z)mH, Z is ethoxy, n+m, on a molar average, is a number of from 5 to 35, two of the substituents R3, R5, R6 and R7 are H and the other two of these substituents are C6H5CHCH3, and preferably, n and m, on a molar average and independently of one another, are numbers of from 2 to 20.
In a further particularly preferred embodiment of the invention in the inventive alkoxylates according to formula (I) X is ethoxy, T is H, R5 is O(Z)mH, Z is ethoxy, n+m, on a molar average, is a number of from 5 to 35, two of the substituents R3, R4, R6 and R7 are H and the other two of these substituents are C6H5CHCH3, and preferably, n and m, on a molar average and independently of one another, are numbers of from 2 to 20.
In a further particularly preferred embodiment of the invention in the inventive alkoxylates according to formula (I) X is ethoxy, T is H, n, on a molar average, is a number of from 5 to 35, R3 is OCH3, two of the substituents R4, R5, R6 and R7 are H and the other two of these substituents are C6H5CHCH3.
In a further particularly preferred embodiment of the invention in the inventive alkoxylates according to formula (I) X is ethoxy, T is H, n, on a molar average, is a number of from 5 to 35, R4 is OCH3, two of the substituents R3, R5, R6 and R7 are H and the other two of these substituents are C6H5CHCH3.
In a further particularly preferred embodiment of the invention in the inventive alkoxylates according to formula (I) X is ethoxy, T is H, n, on a molar average, is a number of from 5 to 35, R5 is OCH3, two of the substituents R3, R4, R6 and R7 are H and the other two of these substituents are C6H5CHCH3.
In an extraordinarily preferred embodiment of the invention in the inventive alkoxylates according to formula (I) X is ethoxy, T is H, n, on a molar average, is a number of from 5 to 35, R3 and R7 are C6H5CHCH3, R4 and R6 are H and R5 is OCH3.
In one preferred embodiment of the invention the inventive alkoxylates such as those according to formula (I) are single compounds.
In another preferred embodiment of the invention the inventive alkoxylates such as those according to formula (I) are mixtures of two or more compounds.
Among the single inventive alkoxylates such as those according to formula (I) and the mixtures of two or more inventive alkoxylates such as those according to formula (I) the mixtures are preferred.
Further preferred embodiments of the invention result from the combination of two or more of the preferred, more preferred, even more preferred, particularly preferred and extraordinarily preferred embodiments of the invention.
The examples below are intended to illustrate the invention in detail without, however, limiting it thereto.
The degree of alkoxylation of the inventive alkoxylates may be checked using NMR spectroscopy. The degree of ethoxylation of described examples was checked using 1H-NMR spectroscopy in analogy to the method described in R. Stevanova, D. Rankoff, S. Panayotova, S. L. Spassov, J. Am. Oil Chem. Soc. 65, 1516-1518 (1988). For this purpose, the samples are derivatised by reacting them with trichloro acetyl isocyanate and measured as solutions in deuterated chloroform containing 1 weight-% (1 wt.-%) of tetramethyl silane as internal standard.
GC-MS spectra were recorded using an Agilent Technologies HP6890 gas chromatograph coupled with an HP 5973 series mass selective detector. Samples were separated on a 15 m×0.25 mm, 0.1 mm film DB-1 UI column. The column temperature was initially held at 40° C. for 2 minutes, then the temperature was raised to 320° C. at a rate of 10° C. per minute and held for 10 minutes. The injector temperature was maintained at 260° C., and the injection volume was 1.0 μL in the split mode. Helium was used as a carrier gas at a pressure of 20 kPa. Mass spectra were scanned from m/z 40-800. The ionization method was El+. All samples were dissolved in organic solvents and filtrated before injection into the GC-system.
The analysis of the reaction mixture was performed by identifying the species by GC-MS and quantification of the peaks by GC FID. The quantification for these compounds is given in GC area percent.
Gas chromatography was performed using a Hewlett Packard GC 6890 with autosampler, coupled with a flame-ionisation detector (fid). Samples were separated on a 15 m×0.32 mm, 0.25 μm film DB-5 column. The column temperature was initially held at 40° C. for 2 minutes, then the temperature was raised to 350° C. at a rate of 25° C. per minute and held for 5 minutes. The injector temperature was maintained at 250° C., the detector temperature was maintained at 330° C. and the injection volume was 1.0 μL in the split mode. Helium was used as a carrier gas with a constant pressure of 0.5 bar. The samples were prepared by diluting 10 mg of sample with 1.5 ml of dichloromethane.
In a 500 ml 3 necked round bottom flask, 110.1 g (1.0 mol) resorcinol and 1.0 g (5.46 mmol) para-toluenesulfonic acid were heated to 120° C. with stirring under nitrogen atmosphere. At 120° C., 312.5 g (3.0 mol) styrene were added dropwise over 1.5 hours. After the addition was completed, the reaction mixture was stirred for 6 hours at 130° C. After cooling down to room temperature, 365.8 g of an orange red solid were obtained.
The composition of the obtained mixture was analyzed by GC-MS and GC. It contained 0.8% distyrenated resorcinol, 93.7% tristyrenated resorcinol and 1.6% tetrastyrenated resorcinol (percentages given are GC area percent).
In a 500 ml 3 necked round bottom flask, 137.6 g (1.25 mol) resorcinol and 1.3 g (6.88 mmol) para-toluenesulfonic acid were heated to 120° C. with stirring under nitrogen atmosphere. At 120° C., 260.4 g (2.5 mol) styrene were added dropwise over 1.5 hours. After the addition was completed, the reaction mixture was stirred for 6 hours at 130° C. After cooling down to room temperature, 379.0 g of a dark red solid were obtained.
The composition of the obtained mixture was analyzed by GC-MS and GC. It contained 9.1% monostyrenated resorcinol, 63.6% distyrenated resorcinol and 25.1% tristyrenated resorcinol (percentages given are GC area percent).
In a 500 ml 3 necked round bottom flask, 155.2 g (1.25 mol) 4-methoxyphenol and 1.3 g (6.88 mmol) para-toluenesulfonic acid were heated to 120° C. with stirring under nitrogen atmosphere. At 120° C., 260.4 g (2.5 mol) styrene were added dropwise over 1.5 hours. After the addition was completed, the reaction mixture was stirred for 2.5 hours at 130° C. After cooling down to room temperature, 407.3 g of a dark orange solid were obtained.
The composition of the obtained mixture was analyzed by GC-MS and GC. It contained 5.0% monostyrenated 4-methoxyphenol, 88.0% distyrenated 4-methoxyphenol and 5.1% tristyrenated 4-methoxyphenol (percentages given are GC area percent).
In a 500 ml 3 necked round bottom flask, 137.6 g (1.25 mol) catechol and 1.3 g (6.88 mmol) para-toluenesulfonic acid were heated to 120° C. with stirring under nitrogen atmosphere. At 120° C., 260.4 g (2.5 mol) styrene were added dropwise over 1.5 hours. After the addition was completed, the reaction mixture was stirred for 1.5 hours at 130° C. After cooling down to room temperature, 375.6 g of a brown-red solid were obtained.
The composition of the obtained mixture was analyzed by GC-MS and GC. It contained 4.9% monostyrenated catechol, 88.3% distyrenated catechol and 4.1% tristyrenated catechol (percentages given are GC area percent).
General procedure for the ethoxylation of styrenated derivatives of hydroxy or alkoxy phenols:
The styrenated phenol was filled into a dry and clean lab autoclave. Sodium methoxide solution in methanol was added under stirring and then the autoclave was purged with nitrogen. After a successful pressure test, the pressure in the autoclave was again reduced to atmospheric pressure. Then full vacuum was applied and the reaction mixture was heated up to 100° C. for removal of methanol. This drying was continued for 2 hours at 100° C. After that, the vacuum was compensated with nitrogen. The reaction mixture was heated to 160° C. At this temperature a safe amount of ethylene oxide (EO) was added and the pressure observed until the reaction started (pressure decreased). In the following 7 to 20 hours the rest of ethylene oxide was added at 160° C. (4-5 bar) and stirring was continued for one to two hours to complete the reaction. Then the reaction mixture was cooled down to 100° C. and vacuum was applied for 30 minutes to remove residual ethylene oxide. After that, the vacuum was compensated with nitrogen, the reaction mixture cooled down to 80° C. and filled into a flask.
202.7 g of the product of example 1 and 1.3 g of sodium methoxide solution (30 wt.-% in methanol) were reacted with 203.7 g of ethylene oxide (10 mol EO/mol) as described in the general procedure for the ethoxylation of styrenated derivatives of hydroxy or alkoxy phenols. 155.9 g of the product (brown oil) were discharged out of the reactor.
The remaining product of example 5 (250.7 g, calculated) was reacted with additional 125.7 g of ethylene oxide (10 mol EO/mol) as described in the general procedure for the ethoxylation of styrenated derivatives of hydroxy or alkoxy phenols. 182.2 g of the product (brown oil) were discharged out of the reactor.
The remaining product of example 6 (194.2 g, calculated) was reacted with additional 64.9 g of ethylene oxide (10 mol EO/mol) as described in the general procedure for the ethoxylation of styrenated derivatives of hydroxy or alkoxy phenols. 259.1 g of the product (brown oil) were obtained.
206.6 g of the product of example 4 and 1.7 g of sodium methoxide solution (30 wt.-% in methanol) were reacted with 280.3 g of ethylene oxide (10 mol EO/mol) as described in the general procedure for the ethoxylation of styrenated derivatives of hydroxy or alkoxy phenols. 212.0 g of the product (brown oil) were discharged out of the reactor.
The remaining product of example 8 (274.9 g, calculated) was reacted with additional 158.3 g of ethylene oxide (10 mol EO/mol) as described in the general procedure for the ethoxylation of styrenated derivatives of hydroxy or alkoxy phenols. 198.2 g of the product (brown oil) were discharged out of the reactor.
The remaining product of example 9 (235.0 g, calculated) was reacted with additional 85.9 g of ethylene oxide (10 mol EO/mol) as described in the general procedure for the ethoxylation of styrenated derivatives of hydroxy or alkoxy phenols. 320.9 g of the product (brown oil) were obtained.
192.3 g of the product of example 2 and 1.5 g of sodium methoxide solution (30 wt.-% in methanol) were reacted with 248.3 g of ethylene oxide (10 mol EO/mol) as described in the general procedure for the ethoxylation of styrenated derivatives of hydroxy or alkoxy phenols. 175.4 g of the product (brown oil) were discharged out of the reactor.
The remaining product of example 11 (265.2 g, calculated) was reacted with additional 149.4 g of ethylene oxide (10 mol EO/mol) as described in the general procedure for the ethoxylation of styrenated derivatives of hydroxy or alkoxy phenols. 179.1 g of the product (brown oil) were discharged out of the reactor.
Ethoxylation of the Product of Example 2 with 30 Equivalents of EO
The remaining product of example 12 (235.5 g, calculated) was reacted with additional 84.9 g of ethylene oxide (10 mol EO/mol) as described in the general procedure for the ethoxylation of styrenated derivatives of hydroxy or alkoxy phenols. 320.4 g of the product (brown oil) were obtained.
Ethoxylation of the Product of Example 3 with 10 Equivalents of EO
208.5 g of the product of example 3 and 1.7 g of sodium methoxide solution (30 wt.-% in methanol) were reacted with 272.3 g of ethylene oxide (10 mol EO/mol) as described in the general procedure for the ethoxylation of styrenated derivatives of hydroxy or alkoxy phenols. 127.8 g of the product (brown oil) were discharged out of the reactor.
The remaining product of example 14 (353.0 g, calculated) was reacted with additional 199.9 g of ethylene oxide (10 mol EO/mol) as described in the general procedure for the ethoxylation of styrenated derivatives of hydroxy or alkoxy phenols. 410.0 g of the product (brown oil) were discharged out of the reactor.
The remaining product of example 15 (142.9 g, calculated) was reacted with additional 51.7 g of ethylene oxide (10 mol EO/mol) as described in the general procedure for the ethoxylation of styrenated derivatives of hydroxy or alkoxy phenols. 194.6 g of the product (brown oil) were obtained.
An aqueous liquid laundry detergent of the following formulation was prepared:
ASP: alkoxylated and styrenated phenol derivative
The formulation was used to wash eight 5×5 cm knitted cotton cloth pieces in a tergotometer set at 200 rpm (revolutions per minute). A one hour wash was conducted in 800 ml of 26° French Hard water at 20° C., with 2.3 g/l of the formulation. To simulate soil that could redeposit, 0.04 g/l of 100% compressed carbon black (ex Alfa Aesar) was added to the wash liquor. To simulate oily sebaceous soil 7.2 g of an SBL2004 soil strip (ex Warwick Equest) was added to the wash liquor.
Once the wash had been completed the cotton swatches were rinsed once in 400 ml clean water, removed, dried and the colour measured on a reflectometer and expressed as the CIE L*a*b* values. The anti-redeposition benefit was expressed as the ΔL value:
ΔL=L(dispersant)−L(control)
The larger the ΔL value the greater the prevention of deposition of the carbon black soil. 95% confidence limits based on the 8 separate cotton swatches were calculated. Formulations were made with and without the addition of 8.7 wt.-% of the dispersant of Table 2. The results are given in Table 2.
The dispersants enhance anti-redeposition.
The formulations of Table 1 including exemplary dispersants of Table 2 were used to wash eight 5×5 cm EMPA 117 stain swatches (blood/milk/ink stain on polycotton) in a tergotometer set at 200 rpm. A 60 minute wash was conducted in 800 ml of 26° French Hard water at 20° C., with 2.3 g/l of the formulation. To simulate oily sebaceous soil 7.2 g of an SBL2004 soil strip (ex Warwick Equest) was added to the wash liquor.
Once the wash had been completed the cotton swatches were rinsed once in 400 ml clean water, removed dried and the colour measured on a reflectometer and expressed as the CIE L*a*b* values.
The cleaning benefit was expressed as the ΔL value:
ΔL=L(dispersant)−L(control)
The larger the ΔL value the greater the prevention of deposition of the carbon black soil. 95% confidence limits based on the 8 separate cotton swatches were calculated. Formulations were made with and without the addition of 8.7 wt.-% of the dispersant of Table 3. The results are given in Table 3.
The dispersants enhance stain removal.
| Number | Date | Country | Kind |
|---|---|---|---|
| 16156197.2 | Feb 2016 | EP | regional |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/EP2017/052241 | 2/2/2017 | WO | 00 |
