Patent Application
20240117279
The present invention provides a soil release polyester polymer which is biodegradable and has favorable soil releasing performance. In another aspect the invention also provides a cleaning composition comprising the same.
Soil release agents are key ingredients in cleaning compositions, i.e., textiles, laundry and hard surfaces such as carpet-cleaning and textile treating.
A variety of soil release compositions have been introduced and are known in the art. The soil release compositions often contain polymers such as amphophilic compounds based on a polyester backbone. These backbones can be copolymers of ethylene glycol and terephthalic acids or polyethylene terephthalate and polyethylene glycol polyester polyether. These polymers consist of hydrophilic and hydrophobic units and are analogous to synthetic fibers such as those found in polyester fabrics which contain terephthalate, ethyleneoxy or propyleneoxy polymeric units. The similarity in chemical structure of soil release polymers and polyester synthetic fabrics allow for binding or deposition of soil release polymers onto fibers and modify surface energy by imparting hydrophilic characteristics to fiber. This results in better cleaning by either retarding the attachment of oily soil to fibers and thus minimizes subsequent soiling or improving the wetting of fibers and susceptibility of a fabric to detergent during washing and thus, to facilitate soil removal.
Soil release polymers (SRPs), especially when they are formulated in cleaning formulations such as a fabric care composition, a dish cleaning composition, a home care composition, a personal care composition or a health care composition, are considered as environmental chemicals, i.e. substances that enter the environment after their use. These chemicals go down to the drain and enter receiving waters directly or after sewage treatment increasing the chemical load of surface waters. Rapid ultimate biodegradation of a soil release polymer to mineralization products (carbon dioxide, water, inorganic salts) is most desirable mechanism for its ultimate removal from sewages, surface waters and soils.
U.S. Pat. No. 6,579,466B1 disclosed a sulphonated polyesters and a detergent composition comprising the same, wherein the sulphonated polyesters showed good antisoilling property, however it doesn't show good biodegradability.
Therefore it is still desirable to develop a soil release polymer which is biodegradable and possess favorable soil releasing performance.
In one aspect of the present invention, it is provided a soil release polyester polymer which is biodegradable and has favorable soil releasing performance. In addition, when applied to fabrics or textiles, the soil release polyester polymer can prevent or reduce degradation thereof, and also protect colors thereof.
In another aspect of the present invention, it is provide a cleaning composition comprising the soil release polyester polymer. The cleaning composition can be a fabric care composition, dish cleaning composition, home care composition, personal care composition or health care composition. In some embodiment of the present invention, the cleaning composition is a product selected from the group consisting of liquid laundry detergents, solid laundry detergents, laundry soap products, laundry spray treatment products, laundry pre-treatment products, hand dish washing detergents, automatic dishwashing detergents, a beauty care detergent, hard surface cleaning detergents, carpet cleaning detergents, a shampoo, and a household cleaning detergent.
Throughout the description, including the claims, the term “comprising one” or “comprising a” should be understood as being synonymous with the term “comprising at least one”, unless otherwise specified. The terms “between” and “from . . . to . . . ” should be understood as being inclusive of the limits.
The articles “a”, “an” and “the” are used to refer to one or to more than one (i.e., to at least one) of the grammatical object of the article.
It should be noted that in specifying any range of concentration, weight ratio or amount, any particular upper concentration, weight ratio or amount can be associated with any particular lower concentration, weight ratio or amount, respectively.
As used herein, the term “alkyl” means a saturated hydrocarbon radical, which may be straight, branched or cyclic, such as, methyl, ethyl, n-propyl, iso-propyl, n-butyl, sec-butyl, t-butyl, pentyl, n-hexyl, cyclohexyl.
As used herein, the terminology “(Cn-Cm)” in reference to an organic group, wherein n and m are each integers, indicates that the group may contain from n carbon atoms to m carbon atoms per group.
Biodegradable Soil Release Polyester Polymer
In one aspect of the present invention, it is provided a biodegradable soil release polyester polymer which is biodegradable and has favorable soil releasing performance. The biodegradable soil release polyester polymer of the present invention can be prepared from a monomer composition comprising:
The sulphonated dicarboxylic acid monomer (SA) has at least one sulphonic acid group, preferably in the form of an alkali metal (preferably sodium) sulphonate, and two acidic functional groups or acidic functional group equivalents (that is to say an anhydride functional group or two ester functional groups) attached to one or a number of aromatic rings, when aromatic dicarboxylic acids or anhydrides or their diesters are involved, or to the aliphatic chain when aliphatic dicarboxylic acids or anhydrides or their alkyl diesters are involved.
Among the sulphonated dicarboxylic acid monomers (SA), there may be mentioned aromatic sulphonated dicarboxylic acids or anhydrides such as sulphoisophthalic, sulphoterephthalic, sulpho-ortho-phthalic acids or anhydrides, 4-sulpho-2,7-naphthalenedicarboxylic acids or anhydrides, sulpho-4,4′-bis(hydroxycarbonyl)diphenyl sulphones, sulphodiphenyldicarboxylic acids or anhydrides, sulpho-4,4′-bis(hydroxycarbonyl)diphenylmethanes, sulpho-5-phenoxyisophthalic acids or anhydrides or their lower (methyl, ethyl, propyl, isopropyl, butyl) diesters and sulphonated aliphatic sulphonated dicarboxylic acids or anhydrides such as sulphosuccinic acids or anhydrides or their lower (methyl, ethyl, propyl, isopropyl, butyl) diester. In one embodiment of the present invention, the sulphonated dicarboxylic acid monomers (SA) are selected from aromatic sulphonated dicarboxylic acids, preferably sulphoisophthalic, sulphoterephthalic, sulpho-ortho-phthalic acids or anhydrides lower diesters thereof.
The polyhydric polyol (P) used in the present invention is at least one polyol selected from the group consisting of ethylene glycol, propylene glycol, diethylene glycol, triethylene glycol, tetraethylene glycol or polyethylene glycol having an ethylene oxide number ranging from 1 to 200, dipropylene glycol, glycerol, 1,2,4-butanetriol and 1,2,3-butanetriol, and oligomers of thereof having from 1 to 100 monomer units; preferably used is ethylene glycol and/or glycerol.
In one embodiment of the present invention, the unsulphonated dicarboxylic acid monomerdicarboxylic acid monomers (A) are consisted of isophthalic and/or furan dicarboxylic acids.
In the unsulphonated dicarboxylic acid monomer (A) there may additionally be present minor quantities of aromatic diacids other than those mentioned above, such as orthophthalic acid, anthracene, 1,8-naphthalene, 1,4-naphthalene and biphenyl dicarboxylic acids or aliphatic diacids such as adipic, glutaric, succinic, trimethyladipic, pimelic, azelaic, sebacic, suberic, itaconic and maleic acids, etc. in the form of acid, anhydride or lower (methyl, ethyl, propyl, isopropyl, butyl) diesters.
The prepolymer c2) used in the present invention is prepared from the unsulphonated dicarboxylic acid monomerdicarboxylic acid monomers (A) or the derivatives thereof and the polyhydric polyol (P). In one embodiment of the present invention, the prepolymer c2) is polyethylene terephthalate which can be prepared from terephthalic acid, isophthalic acid, ethylene glycol and/or diethylene glycol. Preferably the prepolymer c2) has an intrinsic viscosity range between 0.1 to 0.9 dL/g determined according to ASTM method D-4603 and has a maximum melting point of 250° C.
The dihydroxyl compound (DH) used in the present invention is selected from C5-C10 cycloaliphatic diol or C2-C8 hydroxylated aliphatic acid, an aromatic or aliphatic dicarboxylic acid or the combination thereof.
The cycloaliphatic diol is defined as the cycloaliphatic radical substituted by two hydroxyl groups. As used herein the term “cycloaliphatic radical” refers to a radical having a valence of two, and comprising an array of atoms which is cyclic but which is not aromatic. As defined herein a “cycloaliphatic radical” does not contain an aromatic group. A “cycloaliphatic radical” may comprise one or more noncyclic components. For example, a cyclohexylmethyl group (C6H11CH2—) is a cycloaliphatic radical which comprises a cyclohexyl ring (the array of atoms which is cyclic but which is not aromatic) and a methylene group (the noncyclic component). The two hydroxyl groups may attach to the cyclic ring or the noncyclic component. The cycloaliphatic radical may include heteroatoms such as nitrogen, sulfur, selenium, silicon and oxygen, or may be composed exclusively of carbon and hydrogen. For convenience, the term “cycloaliphatic radical” is defined herein to encompass a wide range of functional groups such as alkyl groups, alkenyl groups, alkynyl groups, halo alkyl groups, conjugated dienyl groups, ether groups, and the like.
In one embodiment of the present application, the C5-C10 cycloaliphatic diol is selected from C5-C10 cyclopentyl diol, cyclohexyl diol, or cycloheptyl diol or the combination thereof. The illustrative example of C5-C10 cycloaliphatic diol include but not limited to cyclopentane dimethanol, cyclopentane diethanol, cyclohexane dimethanol, cyclohexane diethanol, cycloheptane dimethanol.
In one embodiment of the present application, the dihydroxyl compound is selected from aliphatic dicarboxylic acid or the derivatives thereof.
As used herein, the term “aliphatic dicarboxylic acid” means carboxylic acids having two carboxyl groups each attached to a saturated carbon atom. If the carbon atom to which the carboxyl group is attached is saturated and is in a ring, the acid is cycloaliphatic.
The illustrative example of aliphatic dicarboxylic acids include but not limited to sebacic acid, 1,3-cyclohexane dicarboxylic acid, 1,4-cyclohexane dicarboxylic acid, adipic acid, glutaric acid, succinic acid, oxalic acid, azelaic acid, diethylmalonic acid, allylmalonic acid, 4-cyclohexene-1,2-dicarboxylic acid, 2-ethylsuberic acid, tetramethylsuccinic acid, cyclopentanedicarboxylic acid, decahydro-1,5-naphthalene dicarboxylic acid, 4,4′-bicyclohexyl dicarboxylic acid, decahydro-2,6-naphthalene dicarboxylic acid, 4,4′-methylene bis(cyclohexane carboxylic acid), 3,4-furan dicarboxylic acid, and 1,1-cyclobutane dicarboxylic acid. Preferred aliphatic dicarboxylic acids are 1,3-cyclohexane dicarboxylic acid, 1,4-cyclohexane dicarboxylic acid.
In one embodiment of the present invention, more than one dihydroxyl compounds can be used, for example, cyclohexane dimethanol and glycolic acid can be used together in the present invention.
In another embodiment of the present invention, the dihydroxyl compound(s) is used in an amount of 0.1% to 50%, preferably between 0.5% to 25%, more preferably between 0.5% to 15%, based on the 100 molar % of the biodegradable soil release polyester polymer.
The biodegradable soil release polyester polymer of the present invention can be prepared by the process of esterification or transesterification and polycondensation according to the common knowledge in the art. U.S. Ser. No. 09/887,664 discloses such a process of preparing the water-dispersible polyester polymer, which are hereby incorporated herein by reference in their entirety.
The Cleaning Composition
In the present invention, it is further provided a cleaning composition, comprising:
In the present invention, the composition is a fabric care composition, dish cleaning composition, home care composition, personal care composition or health care composition.
As used herein, the term “cleaning composition” includes, but is not limited to, laundry cleaning compositions, laundry soap products, fabric care compositions, hard surface cleaning compositions, dish cleaning compositions, home care cleaning compositions, and personal care cleaning compositions, for example, for use in the health and beauty area. Cleaning compositions include granular, powder, liquid (including heavy duty liquid (“HDL”) detergents), gel, paste, bar form and/or flake type cleaning agents, laundry detergent cleaning agents, laundry soak or spray treatments and pre-treatments, fabric treatment compositions, dish washing detergents and soaps, shampoos, hand washing compositions, body washes and soaps, and other similar cleaning compositions.
As used herein, the term “fabric treatment composition” includes, unless otherwise indicated, fabric softening compositions, fabric enhancing compositions, fabric freshening compositions and combinations thereof. Such compositions may be, but need not be wash or rinse added compositions.
As used herein, the term “personal care cleaning composition” includes shampoos, hand washing compositions, body washing compositions, hair removal compositions, bath soaps, bar soaps, bath beads, cosmetics, beauty bars, and lotions.
Examples of cleaning compositions include, but are not limited to, liquid laundry detergents, solid laundry detergents, laundry soap products, laundry spray treatment products, laundry pre-treatment products, hand dish washing detergents, automatic dishwashing detergents, a beauty care detergent, hard surface cleaning detergents, carpet cleaning detergents, a shampoo, and a household cleaning detergent.
Examples of fabric care compositions suitable for the present disclosure include, but are not limited to, liquid laundry detergents, heavy duty liquid laundry detergents, solid laundry detergents, laundry soap products, laundry spray treatment products, laundry pre-treatment products, laundry soak products, heavy duty liquid detergents, and rinse additives.
Examples of suitable dish cleaning compositions include, but are not limited to, automatic dishwasher detergents, detergents for hand washing of dishes, liquid dish soap, and solid granular dish soap.
Examples of suitable home care compositions include, but are not limited to, rug or carpet cleaning compositions, hard surface cleaning detergents, floor cleaning compositions, window cleaning compositions, toilet and bathroom cleaning compositions, household cleaning detergents, and car washing detergents.
Examples of suitable personal care compositions include, but are not limited to, beauty care detergents, beauty bars, bar soap, bath beads, bath soaps, hand washing compositions, body washes and soaps, shampoo, conditioners, cosmetics, and hair removal compositions.
Examples of suitable health care compositions include, but are not limited to, oral and dental care compositions.
In one embodiment of the present invention, the cleaning composition is a laundry detergent composition.
The anionic surfactants contemplated in the present invention as surface-active agent comprise the major active components in conventional detergent systems, including any of the known hydrophobes attached to a carboxylate, sulphonate, sulfate or phosphate polar, solubilizing group including salts. Salts may be the sodium, potassium, ammonium and amine salts of such surfactants. Useful anionic surface-active agents can be organic sulfuric reaction products having in their molecular structure an alkyl group containing from about 8 to about 22 carbon atoms and a sulfonic acid or sulfuric acid ester group, or mixtures thereof. (Included in the term “alkyl” is the alkyl portion of acyl groups.) Examples of this group of synthetic detersive surfactants which can be used in the present invention are the alkyl sulfates, especially those obtained by sulfating the higher alcohols (C8-C18 carbon atoms) produced from the glycerides of tallow or coconut oil; and alkyl benzene sulphonates.
Other useful anionic surface-active agents herein include the esters of alpha-sulphonated fatty acids preferably containing from about 6 to 20 carbon atoms in the ester group; 2-acyloxyalkane-1-sulfonic acids preferably containing from about 2 to 9 carbon atoms in the acyl group and from about 9 to about 23 carbon atoms in the alkane moiety; alkyl ether sulfates preferably containing from about 10 to 20 carbon atoms in the alkyl group and from about 1 to 30 moles of ethylene oxide; olefin sulphonates preferably containing from about 12 to 24 carbon atoms; and beta-alkyloxy alkane sulphonates preferably containing from about 1 to 3 carbon atoms in the alkyl group and from about 8 to 20 carbon atoms in the alkane moiety.
Anionic surface-active agents based on the higher fatty acids, i.e., “soaps” are useful anionic surfactants herein. Higher fatty acids containing from about 8 to about 24 carbon atoms and preferably from about 10 to about 20 carbon atoms and the coconut and tallow soaps can also be used herein as corrosion inhibitors.
Preferred water-soluble anionic organic surfactants herein include linear alkyl benzene sulphonates containing from about 10 to about 18 carbon atoms in the alkyl group; branched alkyl benzene sulphonates containing from about 10 to about 18 carbon atoms in the alkyl group; the tallow range alkyl sulfates; the coconut range alkyl glyceryl sulphonates; alkyl ether (ethoxylated) sulfates wherein the alkyl moiety contains from about 12 to 18 carbon atoms and wherein the average degree of ethoxylation varies between 1 and 12, especially 3 to 9; the sulfated condensation products of tallow alcohol with from about 3 to 12, especially 6 to 9, moles of ethylene oxide; and olefin sulphonates containing from about 14 to 16 carbon atoms.
Specific preferred anionics for use herein include: the linear C10-C14 alkyl benzene sulphonates (LAS); the branched C10-C14 alkyl benzene sulphonates (ABS); the tallow alkyl sulfates, the coconut alkyl glyceryl ether sulphonates; the sulfated condensation products of mixed C10-C18 tallow alcohols with from about 1 to about 14 moles of ethylene oxide; and the mixtures of higher fatty acids containing from 10 to 18 carbon atoms.
It is to be recognized that any of the foregoing anionic surfactants can be used separately herein or as mixtures. Moreover, commercial grades of the surfactants can contain non-interfering components which are processing by-products. For example, commercial alkaryl sulphonates, preferably C10-C14, can comprise alkyl benzene sulphonates, alkyl toluene sulphonates, alkyl naphthalene sulphonates and alkyl poly-benzenoid sulphonates. Such materials and mixtures thereof are fully contemplated for use herein.
Other examples of the anionic surfactants used herein include fatty acid soaps, ether carboxylic acids and salts thereof, alkane sulphonate salts, α-olefin sulphonate salts, sulphonate salts of higher fatty acid esters, higher alcohol sulfate ester or ether ester salts, alkyl, preferably higher alcohol phosphate ester and ether ester salts, and condensates of higher fatty acids and amino acids.
Fatty acid soaps include those having the formula: R—C(O)OM, wherein R is C6 to C22 alkyl and M is preferably sodium.
Salts of ether carboxylic acids and salts thereof include those having the formula: R—(OR1)n—OCH2C(O)OM, wherein R is C6 to C22 alkyl, R1 is C2 to Go, preferably C2 alkyl, and M is preferably sodium.
Alkane sulphonate salts and α-olefin sulphonate salts have the formula: R-SO3M, wherein R is C6 to C22 alkyl or α-olefin, respectively, and M is preferably sodium.
Sulphonate salts of higher fatty acid esters include those having the formula:
RC(O)O—R1—SO3M,
wherein R is C12 to C22 alkyl, R1 is C1 to C16 alkyl and M is preferably sodium.
Higher alcohol sulfate ester salts include those having the formula:
RC(O)O—R1—OSO3M,
wherein R is C12-C22 alkyl, R1 is C1-C18 hydroxyalkyl, M is preferably sodium.
Higher alcohol sulfate ether ester salts include those having the formula:
RC(O)(OCH2CH2)x—R1—OSO3M,
wherein R is C12-C22 alkyl, R1 is C1-C16 hydroxyalkyl, M is preferably sodium and x is an integer from 5 to 25.
Higher alcohol phosphate ester and ether ester salts include compounds of the formulas:
R—(OR1)n—OPO(OH)(OM);
(R—(OR1)n—O)2PO(OM); and
(R—(OR1)n—O)3—PO,
wherein R is alkyl or hydroxyalkyl of 12 to 22 carbon atoms, R1 is C2H4, n is an integer from 5 to 25, and M is preferably sodium.
Other anionic surface-active agents herein are sodium coconut oil fatty acid monoglyceride sulphonates and sulfates; sodium or potassium salts of alkyl phenol ethylene oxide ether sulfates containing from about 1 to about 10 units of ethylene oxide per molecule and wherein the alkyl groups contain from about 8 to about 12 carbon atoms; and sodium or potassium salts of alkyl ethylene oxide ether sulfates containing about 1 to about 10 units of ethylene oxide per molecule and wherein the alkyl group contains from about 10 to about 20 carbon atoms.
The nonionic surfactants which can be contemplated in the present invention as surface-active agent can be one or more selected from the group consisting of:
The catonic surfactants which can be contemplated in the present invention as surface-active agent can be one or more selected from the group consisting of: alkyldimethylammonium halides.
The amphoteric surfactants which can be contemplated in the present invention as surface-active agent can be one or more selected from the group consisting of:
The cleaning compositions of the present invention may further include detergency builders selected from any of the conventional inorganic and organic water-soluble builder salts, including neutral or alkaline salts, as well as various water-insoluble and so-called “seeded” builders.
Builders are preferably selected from the various water-soluble, alkali metal, ammonium or substituted ammonium phosphates, polyphosphates, phosphonates, polyphosphonates, carbonates, silicates, borates, polyhydroxysulphonates, polyacetates, carboxylates, and polycarboxylates. Most preferred are the alkali metal, especially sodium, salts of the above.
Specific examples of inorganic phosphate builders are sodium and potassium tripolyphosphate, pyrophosphate, polymeric metaphosphate having a degree of polymerization of from about 6 to 21, and orthophosphate. Examples of polyphosphonate builders are the sodium and potassium salts of ethylene-1, 1-diphosphonic acid, the sodium and potassium salts of ethane 1-hydroxy-1, 1-diphosphonic acid and the sodium and potassium salts of ethane, 1,1,2-triphosphonic acid.
Examples of non-phosphorus, inorganic builders are sodium and potassium carbonate, bicarbonate, sesquicarbonate, tetraborate decahydrate, and silicate having a molar ratio of SiO2 to alkali metal oxide of from about 0.5 to about 4.0, preferably from about 1.0 to about 2.4.
Water-soluble, non-phosphorus organic builders useful herein include the various alkali metal, ammonium and substituted ammonium polyacetates, carboxylates, polycarboxylates and polyhydroxysulphonates. Examples of polyacetate and polycarboxylate builders are the sodium, potassium, lithium, ammonium and substituted ammonium salts of ethylenediamine tetracetic acid, nitrilotriacetic acid, oxydisuccinic acid, mellitic acid, benzene polycarboxylic acids, and citric acid.
Highly preferred polycarboxylate builders herein are set forth in U.S. Pat. No. 3,308,067 to Diehl, which is again incorporated herein by reference. Such materials include the water-soluble salts of homo- and copolymers of aliphatic carboxylic acids such as maleic acid, itaconic acid, mesaconic acid, fumaric acid, aconitic acid, citraconic acid and methylenemalonic acid.
Other builders include the carboxylated carbohydrates of U.S. Pat. No. 3,723,322 to Diehl which is incorporated herein by reference.
Other useful builders herein are sodium and potassium carboxymethyloxymalonate, carboxymethyloxysuccinate, ciscyclohexanehexacarboxylate, cis-cyclopentanetetracarboxylate phloroglucinol trisulphonate, water-soluble polyacrylates (having molecular weights of from about 2,000 to about 200,000 for example), and the copolymers of maleic anhydride with vinyl methyl ether or ethylene.
Other suitable polycarboxylates for use herein are the polyacetal carboxylates described in U.S. Pat. Nos. 4,144,226, and 4,246,495, both to Crutchfield et al.; both of which are incorporated herein by reference.
“Insoluble” builders include both seeded builders such as 3:1 weight mixtures of sodium carbonate and calcium carbonate; and 2.7:1 weight mixtures of sodium sesquicarbonate and calcium carbonate. Amorphous and crystalline alumino silicates such as hydrated sodium Zeolite A are commonly used in laundry detergent applications. They have a particle size diameter of 0.1 micron to about 10 microns depending on water content of these molecules. These are referred to as ion exchange materials. Crystalline alumino silicates are characterized by their calcium ion exchange capacity. Amorphous alumino silicates are usually characterized by their magnesium exchange capacity. They can be naturally occurring or synthetically derived.
A detailed listing of suitable detergency builders can be found in U.S. Pat. No. 3,936,537 to Baskerville, et al. which is also incorporated herein by reference.
Cleaning composition components may also include any one or more of a number of miscellaneous ingredients including hydrotropes, enzymes (e.g., proteases, amylases and cellulases), enzyme stabilizing agents, pH adjusting agents (monoethanolamine, sodium carbonate, etc.) halogen bleaches (e.g., sodium and potassium dichloroisocyanurates), peroxyacid bleaches (e.g., diperoxydodecane-1,1 2-dioic acid), inorganic per compound bleaches (e.g., sodium perborate), antioxidants as optional stabilizers, reductive agents, activators for per compound bleaches (e.g., tetra-acetylethylenediamine and sodium nonanoyloxybenzene sulphonate), soil suspending agents (e.g., sodium carboxymethyl cellulose), soil anti-redisposition agents, corrosion inhibitors, perfumes and dyes, buffers, whitening agents, solvents (e.g., glycols and aliphatic alcohols) and optical brighteners. Any of other commonly used auxiliary additives such as inorganic salts and common salt, humectants, solubilizing agents, UV absorbers, softeners, chelating agents, static control agents and viscosity modifiers may be added to the cleaning compositions of the invention.
For bar compositions, processing aids are optionally used such as salts and/or low molecular weight alcohols such as monodihydric, dihydric (glycol, etc.), trihydric (glycerol, etc.), and polyhydric (polyols) alcohols. Bar compositions may also include insoluble particulate material components, referred to as “fillers” such as calcium carbonate, silica and the like.
The total weight percentages of the conventional surfactants of the present invention, all weight percentages being based on the total active weight of the compositions of this invention consisting of the nonionic ethoxylate and amphoteric surfactant(s), soil release agent(s), and (optionally) one or more other surfactants, detergency builder(s), additives and the like are about 10 to about 99.9 weight percent, preferably about 15-75 weight percent.
The long chain linear alkyl nonionic alcohol alkoxylates or amphoteric enhancers are combined with said biodegradable soil release polyester polymer in a weight ratio of from about 1:10 to about 10:1 respectively and preferably in a weight ratio of about 1:2 to about 2:1. The nonionic alcohol alkoxylates and amphoteric enhancers are incorporated in the total cleaning composition in an amount of from about 0.1 wt. % to 12 wt. % and preferably in an amount of from about 0.5 to 2.0 wt. %.
The biodegradable soil release polyester polymers are suitably employed at a level of from about 0.05 to about 40 wt. % active weight percent, preferably from about 0.2-15 wt. %, based on the total weight of the detergent formulation. The cmc lowering surfactants are incorporated into said soil release compositions with the soil release agent in a weight ratio of from about 1:10 to 10:1, respectively, and preferably in a weight ratio of about 1:2 to about 1:1. The soil release composition consisting of the soil release polymer and enhancer is incorporated in the total detergent formulation in an amount of from about 0.5 wt. % to about 15.0 wt. %.
The optional detergency builders are suitably present at a level of from about 0 to about 70 weight percent, preferably from about 5 to about 50 weight percent.
In the preparation of detergent and/or fabric softening compositions, other optional ingredients such as bleaches, enzymes, antioxidants, reductive agents, perfumes, fabric brighteners and the like may be included in amounts each of from about 0 to about 5 weight percent based on the active weight of the composition.
When the soil release compositions of the present invention are used in fabric softener compositions, they generally comprise from about 1 to 80 wt. % of a cationic conventional surfactant; and from about 0.005 to about 20, preferably 0.02-10 wt. % of the C12 to C22 amphoteric or long chain nonionic alkoxylate surfactant. They also contain about 0.1 to about 5, preferably about 0.2-3.0, most preferably about 0.2 to about 1.5 wt. % of polymeric soil release agent. Enhancer/polymer synergy enhances soil release and general detergency boosting benefits, and improves suspending/stabilizing properties of the polymeric suspending agents.
Other optional ingredients for liquid detergents include liquid carriers and adjuvants as disclosed by U.S. Pat. No. 5,402,542 to Trinh et al., which is incorporated herein by reference in its entirety.
The cleaning composition of the present invention could be in the form such as granular, powder, liquid, gel, paste, bar or the like. A person skilled in the art can decide suitable carries used in the composition. In case the cleaning composition is a liquid, the liquid carrier is preferably selected from the group consisting of water and mixtures of water and short chain C1-C6 monohydric or polyhydric alcohols. The water used can be distilled, deionized, or tap water. Mixtures of water and up to about 90% of a short chain alcohol such as ethanol, propanol, isopropanol or butanol, ethylene glycol, diethylene glycol, propylene glycol, dipropylene glycol, glycerol and mixtures thereof, are useful as the carrier liquid.
Adjuvants can be added to the softener compositions for their known purposes. Such adjuvants include, but are not limited to, clays, viscosity control agents, perfumes, emulsifiers, preservatives, anti-foaming agents, antioxidants, bactericides, fungicides, brighteners, opacifiers, freeze-thaw control agents, shrinkage control agents, and agents to provide ease of ironing. These adjuvants, if used, are added at their usual levels, generally each of up to about 5% by active weight of the composition.
1. The Preparation of the Biodegradable Soil Release Polymer
The biodegradable soil release polymers were prepared as follows:
To a reaction container, a polyhydric polyol (P) was added slowly to sulphonated dicarboxylic acid monomer (SA) and Tyzor TE (catalyst), and optionally an unsulphonated aromatic diacidic monomer (A), a dihydroxyl compound (DH) with stirring. The resulting mixture was heated to 200° C. and mixed for a short period of time. Water was generated as by-product and removed from the reaction mixture by distillation (under vacuum if necessary) along with excess polyol. The reaction mixture was then heated to 235-240° C., and the prepolymer c2) was added in small portions over a period of time. After completion of prepolymer c2) addition, the reaction mixture was heated to 250° C. and kept for a period of time under vacuum to achieve the desired degree of polymerization. The molecular weight (Mw and Mn) was determined by Gel permeation chromatography (GPC) analysis method.
2. The Biodegradability Test
The biodegradability test is done according OECD (1992), Test No. 302B: Inherent Biodegradability: Zahn-Wellens/EVPA Test, OECD Guidelines for the Testing of Chemicals, Section 3, OECD Publishing, Paris.
If the biodegradability test result is over 70%, it will be deemed as passing the biodegradability test.
As shown in the table 1, the biodegradable SRP polymers of the present invention has better biodegradability than those don't comprise dihydroxyl compound (DH).
3. The Soil Release Performance Test
The soil release polymers tested are introduced into the ECE(A) standard test detergent no. 2 according to ISO 105 C-08. ECE is the European colourfastness establishment. The composition of the ECE(A) standard test detergent no. 2 according to ISO 105 C-08 is shown in Table 2. The proportion of the soil release polymers in the ECE(A) no. 2 detergent is 1.0% by weight of polymer active substance.
The soil release performance is carried out on the following test fabrics:
Prewashing:
The test fabrics were cut into squares 7 cm×7 cm in size in three replicates and were prewashed in a Tergotometer for 20 minutes at 40° C. with the washing powder compositions shown in Table 2. The water employed had a hardness of 25° FH and the quantity of the washing powder used was 5 grams per liter of water. The Tergotometer speed was set at 120 oscillations per minute.
The test fabric squares were then rinsed 3 times for 5 minutes with cold water (20° C.) and then dried.
Staining:
After the test fabric squares were completely dried, they were stained using three drops of dirty motor oil (DMO) added from a 3 ml disposable pipette. The stained test fabric squares were left overnight before washing. To allow good reproducibility of the results the stained test fabrics squares were washed within 24 hours.
Washing:
The washing was performed in the same conditions as the prewashing in a Tergotometer for 20 minutes at 40° C. with the washing powder compositions shown in Table 2. The water employed had a hardness of 25° FH and the quantity of the washing powder used was 5 grams per liter of water. The Tergotometer speed was set at 120 oscillations per minute.
The test fabric squares were then rinsed 3 times for 5 minutes with cold water (20° C.) and then dried.
Evaluation:
The test fabric squares before staining (referred to as white), after staining (referred to as stain) and after washing (referred to as wash) were analyzed with the ColorQuest XE reflectance colorimeter from HunterLab to measure its initial CIEALAB color space (L*, a*, b*).
The effectiveness of the soil release polymers according to the present invention is assessed as the % of removal of the stain, calculated by the formula:
Where:
ΔL=L*(wash)−L*(stain)
Δa=a*(wash)−a*(stain)
Δb=b*(wash)−b*(stain)
ΔL′=L*(white)−L*(stain)
Δa′=a*(white)−a*(stain)
Δb′=b*(white)−b*(stain)
The average of the % of stain removal is calculated for each test fabric. The results obtained are given in Table 3 which follows:
As shown in table 3, compared to ECE(A) no. 2, SRP polymers, including the comparative example 1, can improve the soil releasing performance of the washing powder composition comprising the same. Compared to the example 4 which SRP polymer 2 is comprised, the example 3 which SRP polymer 1 is comprised has better soil releasing performance.
In general, the soil release polyester polymer of the present application not only has favorable biodegradability but also soil releasing performance, and compared to the SRP polymer of example 2, the SRP polymer of example 1 not only has favorable degradability but also shows better soil releasing performance, thus is more preferred than example 2.
| Number | Date | Country | Kind |
|---|---|---|---|
| PCT/EP2021/052920 | Feb 2021 | WO | international |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/EP2022/052889 | 2/7/2022 | WO |
