EP0371534B1 - Fabric treatment composition - Google Patents
Fabric treatment composition Download PDFInfo
- Publication number
- EP0371534B1 EP0371534B1 EP89202890A EP89202890A EP0371534B1 EP 0371534 B1 EP0371534 B1 EP 0371534B1 EP 89202890 A EP89202890 A EP 89202890A EP 89202890 A EP89202890 A EP 89202890A EP 0371534 B1 EP0371534 B1 EP 0371534B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- water
- fabric
- cationic
- insoluble
- weight
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000000203 mixture Substances 0.000 title claims description 74
- 239000004744 fabric Substances 0.000 title claims description 33
- 239000000463 material Substances 0.000 claims description 94
- 229930195733 hydrocarbon Natural products 0.000 claims description 49
- 150000002430 hydrocarbons Chemical class 0.000 claims description 47
- 239000004215 Carbon black (E152) Substances 0.000 claims description 46
- 125000002091 cationic group Chemical group 0.000 claims description 37
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 20
- 125000000217 alkyl group Chemical group 0.000 claims description 13
- 150000001412 amines Chemical class 0.000 claims description 12
- 239000007788 liquid Substances 0.000 claims description 9
- 125000003342 alkenyl group Chemical group 0.000 claims description 5
- 239000011149 active material Substances 0.000 claims description 4
- 239000004665 cationic fabric softener Substances 0.000 claims description 4
- 238000005406 washing Methods 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
- 150000001875 compounds Chemical class 0.000 claims description 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 3
- 125000004432 carbon atom Chemical group C* 0.000 description 11
- 239000003795 chemical substances by application Substances 0.000 description 10
- IQDGSYLLQPDQDV-UHFFFAOYSA-N dimethylazanium;chloride Chemical compound Cl.CNC IQDGSYLLQPDQDV-UHFFFAOYSA-N 0.000 description 8
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 6
- 125000001183 hydrocarbyl group Chemical group 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 235000019271 petrolatum Nutrition 0.000 description 6
- 239000004615 ingredient Substances 0.000 description 5
- 239000002480 mineral oil Substances 0.000 description 5
- 235000010446 mineral oil Nutrition 0.000 description 5
- 239000003760 tallow Substances 0.000 description 5
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 4
- 239000004902 Softening Agent Substances 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- QLAJNZSPVITUCQ-UHFFFAOYSA-N 1,3,2-dioxathietane 2,2-dioxide Chemical compound O=S1(=O)OCO1 QLAJNZSPVITUCQ-UHFFFAOYSA-N 0.000 description 3
- 244000060011 Cocos nucifera Species 0.000 description 3
- 235000013162 Cocos nucifera Nutrition 0.000 description 3
- 229920000742 Cotton Polymers 0.000 description 3
- 239000002752 cationic softener Substances 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- MTNDZQHUAFNZQY-UHFFFAOYSA-N imidazoline Chemical class C1CN=CN1 MTNDZQHUAFNZQY-UHFFFAOYSA-N 0.000 description 3
- -1 mono-long chain amine Chemical class 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 239000002304 perfume Substances 0.000 description 3
- 150000003856 quaternary ammonium compounds Chemical class 0.000 description 3
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 description 2
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 241001520299 Phascolarctos cinereus Species 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 150000001450 anions Chemical group 0.000 description 2
- DMSMPAJRVJJAGA-UHFFFAOYSA-N benzo[d]isothiazol-3-one Chemical compound C1=CC=C2C(=O)NSC2=C1 DMSMPAJRVJJAGA-UHFFFAOYSA-N 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- 230000003750 conditioning effect Effects 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 230000008021 deposition Effects 0.000 description 2
- 150000004985 diamines Chemical class 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- PGZPBNJYTNQMAX-UHFFFAOYSA-N dimethylazanium;methyl sulfate Chemical compound C[NH2+]C.COS([O-])(=O)=O PGZPBNJYTNQMAX-UHFFFAOYSA-N 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 150000002191 fatty alcohols Chemical class 0.000 description 2
- 239000012467 final product Substances 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
- YQEMORVAKMFKLG-UHFFFAOYSA-N glycerine monostearate Natural products CCCCCCCCCCCCCCCCCC(=O)OC(CO)CO YQEMORVAKMFKLG-UHFFFAOYSA-N 0.000 description 2
- SVUQHVRAGMNPLW-UHFFFAOYSA-N glycerol monostearate Natural products CCCCCCCCCCCCCCCCC(=O)OCC(O)CO SVUQHVRAGMNPLW-UHFFFAOYSA-N 0.000 description 2
- 150000004820 halides Chemical class 0.000 description 2
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 2
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 2
- 235000011007 phosphoric acid Nutrition 0.000 description 2
- 229920000768 polyamine Polymers 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- 239000003755 preservative agent Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- XFNJVJPLKCPIBV-UHFFFAOYSA-N trimethylenediamine Chemical compound NCCCN XFNJVJPLKCPIBV-UHFFFAOYSA-N 0.000 description 2
- JLJNZJNPAYILPJ-XYJRJTJESA-M 1-[1-[(z)-octadec-9-enyl]-4,5-dihydroimidazol-1-ium-1-yl]tetradecan-1-ol;chloride Chemical compound [Cl-].CCCCCCCC\C=C/CCCCCCCC[N+]1(C(O)CCCCCCCCCCCCC)CCN=C1 JLJNZJNPAYILPJ-XYJRJTJESA-M 0.000 description 1
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 1
- BIWFJGMQTHQTJE-UHFFFAOYSA-N 3-ethyl-4,5-dihydro-1h-imidazol-3-ium;chloride Chemical compound Cl.CCN1CCN=C1 BIWFJGMQTHQTJE-UHFFFAOYSA-N 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N Benzoic acid Natural products OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
- 0 CCCNCCC(C)(C)* Chemical compound CCCNCCC(C)(C)* 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 239000004150 EU approved colour Substances 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 229920002907 Guar gum Polymers 0.000 description 1
- 239000004166 Lanolin Substances 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 230000001153 anti-wrinkle effect Effects 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 239000003125 aqueous solvent Substances 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- WXBLLCUINBKULX-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1.OC(=O)C1=CC=CC=C1 WXBLLCUINBKULX-UHFFFAOYSA-N 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 239000007844 bleaching agent Substances 0.000 description 1
- 238000005282 brightening Methods 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 150000001767 cationic compounds Chemical class 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 239000010779 crude oil Substances 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- VKKVMDHHSINGTJ-UHFFFAOYSA-M di(docosyl)-dimethylazanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCCCCCCCC VKKVMDHHSINGTJ-UHFFFAOYSA-M 0.000 description 1
- OCTAKUVKMMLTHX-UHFFFAOYSA-M di(icosyl)-dimethylazanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCCCCCC OCTAKUVKMMLTHX-UHFFFAOYSA-M 0.000 description 1
- HPDYVEVTJANPRA-UHFFFAOYSA-M diethyl(dihexadecyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+](CC)(CC)CCCCCCCCCCCCCCCC HPDYVEVTJANPRA-UHFFFAOYSA-M 0.000 description 1
- ZCPCLAPUXMZUCD-UHFFFAOYSA-M dihexadecyl(dimethyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCC ZCPCLAPUXMZUCD-UHFFFAOYSA-M 0.000 description 1
- REZZEXDLIUJMMS-UHFFFAOYSA-M dimethyldioctadecylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCCCC REZZEXDLIUJMMS-UHFFFAOYSA-M 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000002979 fabric softener Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 239000003349 gelling agent Substances 0.000 description 1
- 230000002070 germicidal effect Effects 0.000 description 1
- 150000002314 glycerols Chemical class 0.000 description 1
- 239000000665 guar gum Substances 0.000 description 1
- 229960002154 guar gum Drugs 0.000 description 1
- 235000010417 guar gum Nutrition 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000003752 hydrotrope Substances 0.000 description 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 1
- 150000002462 imidazolines Chemical class 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 238000010409 ironing Methods 0.000 description 1
- 235000015110 jellies Nutrition 0.000 description 1
- 239000008274 jelly Substances 0.000 description 1
- 229940039717 lanolin Drugs 0.000 description 1
- 235000019388 lanolin Nutrition 0.000 description 1
- 239000011344 liquid material Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical compound COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 239000003605 opacifier Substances 0.000 description 1
- 229940006093 opthalmologic coloring agent diagnostic Drugs 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000006179 pH buffering agent Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- 230000005588 protonation Effects 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 238000007616 round robin method Methods 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000008247 solid mixture Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 239000004034 viscosity adjusting agent Substances 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/0005—Other compounding ingredients characterised by their effect
- C11D3/001—Softening compositions
- C11D3/0015—Softening compositions liquid
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/18—Hydrocarbons
Definitions
- the present invention relates to a fabric-treatment composition, which is especially suitable for use in the rinse cycle of a fabric washing process.
- the present invention relates to a fabric-treatment composition comprising a water-insoluble, cationic fabric-conditioning material and a hydrocarbon material.
- EP-A-0032267 discloses concentrated textile treatment compositions containing a water-insoluble cationic softener, and a long chain hydrocarbon. A specific mono-long chain amine or amine derived compound is included for viscosity control.
- It is an object of the present invention to provide a fabric-treatment composition comprising a water-insoluble, cationic fabric treatment material and a hydrocarbon material. It is another object of the present invention to provide a fabric-treatment composition for enhanced anti-wrinkling of fabrics treated with this composition. Further objects of the present invention are the provision of a fabric-treatment composition which is easy to manufacture at low material costs, which is stable at storage conditions and which is of satisfactory viscosity, especially at high active levels.
- the present invention relates to a liquid fabric-treatment composition
- a liquid fabric-treatment composition comprising an aqueous base, a water-insoluble, cationic fabric-conditioning material and a fabric-substantive hydrocarbon material, wherein the total level of water-insoluble, cationic material and hydrocarbon material is more than 12% and preferably up to 60% by weight of the composition and wherein the weight ratio of water-insoluble, cationic material to hydrocarbon material is between 1:4 and 1:10 as defined in the appended claim 1.
- the water-insoluble, cationic fabric softener can be any fabric-substantive cationic compound that has a solubility in water at pH 2.5 and 20°C of less than 10 g/l.
- Highly preferred materials are quaternary ammonium salts having two C12-C24 alkyl or alkenyl chains, optionally substituted or interrupted by functional groups such as -OH, -O-, -CONH and -COO-.
- R1 and R2 represent hydrocarbyl groups of from 12 to 24 carbon atoms
- R3 and R4 represent hydrocarbyl groups containing from 1 to 4 carbon atoms
- R1 ⁇ 4 may optionally be substituted or interrupted by functional groups such as -OH, -O-, -CONH- or -COO-
- X is an anion, preferably selected from halide, methyl sulphate and ethyl sulphate radicals.
- quaternary softeners include ditallow dimethyl ammonium chloride, ditallow dimethyl ammonium methyl sulphate, dihexadecyl dimethyl ammonium chloride, di(hydrogenated tallow alkyl) dimethyl ammonium chloride, dioctadecyl dimethyl ammonium chloride, dieicosyl dimethyl ammonium chloride, didocosyl dimethyl ammonium chloride, di(hydrogenated tallow) dimethyl ammonium methyl sulphate, dihexadecyl diethyl ammonium chloride and di(coconut alkyl) dimethyl ammonium chloride.
- Ditallow dimethyl ammonium chloride, di(hydrogenated tallow alkyl) dimethyl ammonium chloride, di(coconut alkyl) dimethyl ammonium chloride and di(coconut alkyl) dimethyl ammonium methosulphate are preferred.
- Other preferred quaternary ammonium compounds are disclosed in EP-A-239 910.
- alkyl imidazolinium salts believed to have the formula: wherein R6 is an alkyl or hydroxyalkyl group containing from 1 to 4, preferably 1 or 2 carbon atoms, R7 is an alkyl or alkenyl group containing from 8 to 25 carbon atoms, R8 is an alkyl or alkenyl group containing from 8 to 25 carbon atoms, and R9 is hydrogen or an alkyl group containing from 1 to 4 carbon atoms and A ⁇ is an anion, preferably a halide, methosulphate or ethosulphate.
- Preferred imidazolinium salts include 1-methyl-1-(tallowylamido) ethyl-2-tallowyl-4,5-dihydroimidazolinium methosulphate and 1-methyl-1-(palmitoylamido) ethyl-2-octadecyl-4,5-dihydroimidazolinium chloride.
- Other useful imidazolinium materials are 2-heptadecyl-1-methyl-1-(2-stearylamido) ethyl-imidazolinium chloride and 2-lauryl-1-hydroxyethyl-1-oleyl-imidazolinium chloride.
- Also suitable herein are the imidazolinium fabric-softening components of U.S. Patent N° 4,127,489.
- Suitable cationic softener materials for use in compositions of the present invention are amines which are used at relatively low pH values to effect at least the partial protonation thereof.
- Suitable water-insoluble amine fabric softeners have, in protonated form, a solubility in water at pH 2.5 and 20°C of less than 10 g/l.
- the relatively insoluble amine materials are selected from the following groups:
- R15 is a C6 to C24, hydrocarbyl group
- R16 is a C1 to C24 hydrocarbyl group
- R17 is a C1 to C10 hydrocarbyl group.
- Suitable amines include those materials from which the quaternary ammonium compounds disclosed above are derived, in which R15 is R1, R16 is R2 and R17 is R3.
- the amine is such that both R15 and R16 are C6-C20 alkyl preferably C12 ⁇ 20 with C16-C18 being most preferred and with R17 as C1 ⁇ 3 alkyl, or R15 is an alkyl or alkenyl group with at least 22 carbon atoms and R16 and R12 are C1 ⁇ 3 alkyl.
- these amines are protonated with hydrochloric acid, orthophosphoric acid (OPA), C1 ⁇ 5 carboxylic acids or any other similar acids suitable for use in the fabric conditioning compositions of the invention.
- hydrochloric acid orthophosphoric acid (OPA)
- OPA orthophosphoric acid
- C1 ⁇ 5 carboxylic acids or any other similar acids suitable for use in the fabric conditioning compositions of the invention.
- the hydrocarbon material can be any fabric-substantive hydrocarbon material suitable for inclusion in fabric treatment compositions.
- Suitable hydrocarbon materials include hydrocarbon materials comprising a linear or branched alkyl chain and comprising an average of from 12 to 50 carbon atoms per molecule, preferably from 12 to 30 carbon atoms.
- the hydrocarbon materials are either alkanes or alkenes or mixtures thereof; relatively small amounts of non-alkyl substituent groups may be present, provided the hydrocarbon nature of the product is not substantially affected.
- the softening temperature of the hydrocarbon material should preferably be less than 60°C, more preferably less than 50°C, most preferably less than 40°C.
- the hydrocarbon material can be either solid, semi-solid or liquid at room temperature.
- suitable hydrocarbon materials are the liquid hydrocarbon materials of natural source and other liquid hydrocarbon materials including the liquid fractions derived from crude oil, such as mineral oil or liquid paraffins and branched hydrocarbons.
- solid or semi-solid hydrocarbon materials are the paraffinic materials of longer average chain length and the hydrogenated version of the liquid materials mentioned above.
- a particularly useful combination of hydrocarbon materials is a mixture of mineral oil (M85 ex Daltons) and petroleum jelly (Silkolene 910 ex Daltons).
- Mineral oil is a liquid mixture of linear and branched hydrocarbons having an average number of 26 carbon atoms per molecule.
- Petroleum jelly is a semi-solid mixture of linear and branched hydrocarbons having an average number of 26 carbon atoms per molecule and having a softening temperature of about 50°C.
- Fabric-treatment compositions according to the present invention will generally have a total level of water-insoluble, cationic material and hydrocarbon material of from more than 12 to 60% by weight, the remaining of the composition being predominantly water optionally plus minors.
- the total amount of water-insoluble, cationic material and hydrocarbon material is more than 14% by weight, more preferably between 14 and 50% by weight, most preferably between 16 and 45%, typically from 20 to 35 % by weight.
- the pH of the composition is preferably between 2 and 7, more preferably from 3 and 6, especially preferred from 3 to 4.5; the viscosity of the composition is preferably less than 200 cPs at 110 S-1 (Haake viscometer).
- the fabric-treatment composition may comprise one or more ingredients which are suitable for incorporation in fabric-treatment compositions.
- these optional ingredients are nonionic, amphoteric or zwitterionic fabric-treatment materials.
- compositions may also contain, in addition to the cationic fabric softening agent, other non-cationic fabric softening agents, such as nonionic fabric softening agents.
- Suitable nonionic fabric softening agents include glycerol esters, such as glycerol mono-stearate, fatty alcohols, such as stearyl alcohol, alkoxylated fatty alcohols C9-C24 fatty acids and lanolin and derivatives thereof.
- Suitable materials are disclosed in European Patent Application 88 520 (Unilever PLC/NV case C 1325), 122 141 (Unilever PLC/NV case C 1363) and 79 746 (Procter and Gamble). Typically such materials are included at a level within the range of from 0.5% to 10% by weight of the composition.
- compositions may also contain one or more ingredients selected from non-aqueous solvents such as C1-C4 alkanols and polyhydric alcohols, pH-buffering agents such as weak acids, e.g. phosphoric, benzoic or citric acid (the pH of the compositions being preferably less than 6.0), rewetting agents, viscosity modifiers, silicones, anti-gelling agents, perfumes, perfume carriers, fluorescers, colourants, hydrotropes, anti-foaming agents, anti-redeposition agents, enzymes, optical brightening agents, opacifiers, stabilizers such as guar gum and polyethylene glycol, anti-shrinking agents, anti-wrinkle agents, fabric-crisping agents, spotting agents, soil-release agents, germicides, silicones, fungicides, antioxidants, anti-corrosion agents, preservatives, dyes, bleaches and bleach precursors, drape-imparting agents and antistatic agents.
- pH-buffering agents such as
- the level of solvent materials as referred to above is less than the level of cationic fabric softener materials in the composition. More preferably the level of solvents is less than 75 %, more preferred less than 50 % based on the weight of the cationic fabric softener material. Typically compositions of the invention are substantially free from solvents.
- the fabric-treatment composition according to the invention also comprises a small amount of water-soluble, cationic material.
- suitable materials of this nature are given in GB-A-1,601,360.
- Other suitable water-soluble cationic materials include polyamine materials, preferably diamine materials, wherein each nitrogen atom is connected to three other atoms.
- a preferred diamine, water-soluble, cationic material of this nature is Ethoduomeen T13 (ex AKZO) which comprises an N,N',N'-tris (2-hydroxyethyl) N-tallow 1,3-diaminopropane.
- the amount of water-soluble, cationic material is preferably less than the amount of water-insoluble, cationic material.
- the amount of water-soluble, cationic material will preferably be from 0.5 to 10% by weight of the composition.
- compositions according to the invention can be prepared by any method suitable for preparing dispersed, emulsified systems.
- a preferred method involves the forming of a molten pre-mixture of the active materials in water at an elevated temperature, adding additional water to obtain the desired active concentration, and then cooling to ambient temperature. When desired, some minor ingredients such as electrolytes, colouring agents, etc. may be post-dosed.
- a second preferred method involves the forming of the product by phase inversion of a water in hydrocarbon emulsion, wherein the cationic softener is either part of the hydrocarbon phase or is added as a separate dispersion after phase inversion. This method is especially advantageous, because this provides very finely divided hydrocarbon particles in the final product.
- the fabric-treatment compositions according to the invention are preferably used in the final rinse of the washing cycle of an ordinary washing machine.
- the amount of fabric-treatment composition to be added is mainly dependent on the active concentration of the composition and the volume of the water used in the rinsing cycle.
- the dose is chosen such that the concentration of active material (softener plus hydrocarbon material) in the rinse water is from 0.05 to 3.0 g/l, preferably from 0.5 to 2.0 g/l.
- Fabric-treatment compositions A-D were prepared as follows: The cationic materials and the hydrocarbon materials were mixed, melted and heated to a temperature of 70°C. The molten actives were added to water of 70°C while mixing at a high speed with a Silverson mixer. After being mixed for 10 minutes, the compositions were cooled to room temperature by rapid chilling in an ice bath while being gently stirred.
- compositions were tested as follows :
- the viscosity of the compositions was measured by a Haake viscometer at ambient temperature. Values are quoted at 110 S ⁇ 1.
- Fig. 1 The results of the tested compositions are represented in Fig. 1.
- This Figure clearly shows that the creasing score increases by decreasing the ratio water-soluble cationic material to hydrocarbon material. From the Figure it is clear that at ratios of 1:2 or higher, the viscosity of the compositions is unacceptably high. At ratios from 1:2 to 1:3, a significant decrease in creasing score is observed. At ratios of 1:4 and lower, a satisfactory creasing score in combination with an adequate viscosity is obtained.
- Fabric-treatment compositions were prepared according to the method as described in Example I. The following compositions were obtained :
- compositions were tested according to the method of Example I.
- the results of the tests are represented in Fig. 2. These results clearly illustrate a relatively high viscosity for compositions of a ratio water-insoluble cationics to hydrocarbon mixture of 1:3 and higher. An acceptably low viscosity is obtained when ratios lower than 1:3 are used.
- the results also illustrate a consistent decrease in wrinkling score in lowering the ratio from 1:2 to 1:3, and an unexpected increase in creasing score at ratios of 1:4 and lower. The combination of acceptable viscosity and adequate creasing score is only found at ratios of 1:4 and lower.
- compositions were made by preheating the Sirius 85, the Silkolene 920, the Adogen 462, the GMS and the Dobanol 25-3 to 60°C and adding water to this premix under stirring.
- This provides a water in oil type emulsion, which upon further addition of water is phase reversed to a oil in water type emulsion, wherein the oil phase is very finely dispersed.
- a predispersion of the Adogen 442 and the Etoduomeeen T13 which had been prepared by heating the two materials to 60°C followed by the addition to water under stirring.
- the final product is obtained by adding the remaining ingredients to the mixture of the two dispersions.
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Chemical Or Physical Treatment Of Fibers (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB888827698A GB8827698D0 (en) | 1988-11-28 | 1988-11-28 | Fabric-treatment composition |
GB8827698 | 1988-11-28 |
Publications (3)
Publication Number | Publication Date |
---|---|
EP0371534A2 EP0371534A2 (en) | 1990-06-06 |
EP0371534A3 EP0371534A3 (en) | 1991-08-28 |
EP0371534B1 true EP0371534B1 (en) | 1996-04-24 |
Family
ID=10647557
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP89202890A Expired - Lifetime EP0371534B1 (en) | 1988-11-28 | 1989-11-15 | Fabric treatment composition |
Country Status (9)
Country | Link |
---|---|
EP (1) | EP0371534B1 (ja) |
JP (1) | JPH02191766A (ja) |
AU (1) | AU626352B2 (ja) |
BR (1) | BR8905986A (ja) |
CA (2) | CA2003494C (ja) |
DE (1) | DE68926334T2 (ja) |
ES (1) | ES2085861T3 (ja) |
GB (1) | GB8827698D0 (ja) |
ZA (1) | ZA899065B (ja) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2281316A (en) * | 1993-08-24 | 1995-03-01 | Sasol Chemical Ind | Fabric treatment composition |
GB9926560D0 (en) | 1999-11-09 | 2000-01-12 | Unilever Plc | Improving the crease recovery of fabrics |
EP1279726A1 (en) * | 2001-07-27 | 2003-01-29 | Givaudan SA | Fabric softener composition |
GB0623005D0 (en) * | 2006-11-17 | 2006-12-27 | Unilever Plc | Fabric treatment method and composition |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0013780B2 (en) * | 1979-01-11 | 1988-08-31 | THE PROCTER & GAMBLE COMPANY | Concentrated fabric softening composition |
EP0018039B2 (en) * | 1979-04-21 | 1988-08-24 | THE PROCTER & GAMBLE COMPANY | Fabric softening composition |
JPS56148970A (en) * | 1980-01-11 | 1981-11-18 | Procter & Gamble | Composition for treating thick clothes |
EP0032267A1 (en) * | 1980-01-11 | 1981-07-22 | THE PROCTER & GAMBLE COMPANY | Concentrated textile treatment compositions and method for preparing them |
US4454049A (en) * | 1981-11-14 | 1984-06-12 | The Procter & Gamble Company | Textile treatment compositions |
US4464273A (en) * | 1982-02-10 | 1984-08-07 | Lever Brothers Company | Fabric softening composition |
AU605825B2 (en) * | 1987-01-29 | 1991-01-24 | Unilever Plc | Fabric conditioning composition |
-
1988
- 1988-11-28 GB GB888827698A patent/GB8827698D0/en active Pending
-
1989
- 1989-11-15 EP EP89202890A patent/EP0371534B1/en not_active Expired - Lifetime
- 1989-11-15 ES ES89202890T patent/ES2085861T3/es not_active Expired - Lifetime
- 1989-11-15 DE DE68926334T patent/DE68926334T2/de not_active Expired - Fee Related
- 1989-11-21 CA CA002003494A patent/CA2003494C/en not_active Expired - Fee Related
- 1989-11-21 CA CA002003493A patent/CA2003493C/en not_active Expired - Fee Related
- 1989-11-24 AU AU45531/89A patent/AU626352B2/en not_active Ceased
- 1989-11-28 BR BR898905986A patent/BR8905986A/pt not_active IP Right Cessation
- 1989-11-28 ZA ZA899065A patent/ZA899065B/xx unknown
- 1989-11-28 JP JP1308844A patent/JPH02191766A/ja active Pending
Also Published As
Publication number | Publication date |
---|---|
DE68926334T2 (de) | 1996-09-19 |
CA2003494A1 (en) | 1990-05-28 |
EP0371534A3 (en) | 1991-08-28 |
ZA899065B (en) | 1991-07-31 |
ES2085861T3 (es) | 1996-06-16 |
CA2003494C (en) | 1996-12-17 |
JPH02191766A (ja) | 1990-07-27 |
CA2003493A1 (en) | 1990-05-28 |
BR8905986A (pt) | 1990-06-19 |
EP0371534A2 (en) | 1990-06-06 |
DE68926334D1 (de) | 1996-05-30 |
AU4553189A (en) | 1990-05-31 |
CA2003493C (en) | 2001-01-09 |
AU626352B2 (en) | 1992-07-30 |
GB8827698D0 (en) | 1988-12-29 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP0199383B1 (en) | Textile treatment compositions | |
EP0056695B2 (en) | Textile treatment compositions | |
US4954270A (en) | Fabric softening composition: fabric softener and hydrophobically modified nonionic cellulose ether | |
EP0326213B1 (en) | A fabric treatment composition and the preparation thereof | |
EP0404471B1 (en) | Fabric softening composition | |
EP0060003A2 (en) | Textile treatment compositions and preparation thereof | |
EP0276999B1 (en) | Fabric conditioning composition | |
EP0593542B1 (en) | Fabric softening composition | |
EP0371535A2 (en) | Fabric treatment composition | |
EP0332270B2 (en) | Fabric conditioning composition | |
US4622154A (en) | Aqueous fabric softening composition | |
CA1204563A (en) | Liquid fabric-softening composition | |
EP0371534B1 (en) | Fabric treatment composition | |
EP0387064A2 (en) | Fabric conditioning | |
EP0159918A2 (en) | Fabric softening composition | |
EP0159919A2 (en) | Aqueous concentrated fabric softening composition | |
EP0159196A2 (en) | Aqueous concentrated fabric softening composition | |
GB2197666A (en) | Method of preparing fabric softening compositions | |
JPH0213065B2 (ja) | ||
EP0159922A2 (en) | Aqueous fabric softening composition |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
AK | Designated contracting states |
Kind code of ref document: A2 Designated state(s): CH DE ES FR GB IT LI NL SE |
|
PUAL | Search report despatched |
Free format text: ORIGINAL CODE: 0009013 |
|
AK | Designated contracting states |
Kind code of ref document: A3 Designated state(s): CH DE ES FR GB IT LI NL SE |
|
17P | Request for examination filed |
Effective date: 19920110 |
|
RAP3 | Party data changed (applicant data changed or rights of an application transferred) |
Owner name: UNILEVER PLC Owner name: UNILEVER N.V. |
|
17Q | First examination report despatched |
Effective date: 19940506 |
|
GRAA | (expected) grant |
Free format text: ORIGINAL CODE: 0009210 |
|
AK | Designated contracting states |
Kind code of ref document: B1 Designated state(s): CH DE ES FR GB IT LI NL SE |
|
REG | Reference to a national code |
Ref country code: CH Ref legal event code: NV Representative=s name: R. A. EGLI & CO. PATENTANWAELTE |
|
REF | Corresponds to: |
Ref document number: 68926334 Country of ref document: DE Date of ref document: 19960530 |
|
REG | Reference to a national code |
Ref country code: ES Ref legal event code: FG2A Ref document number: 2085861 Country of ref document: ES Kind code of ref document: T3 |
|
ITF | It: translation for a ep patent filed | ||
ET | Fr: translation filed | ||
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: CH Payment date: 19961030 Year of fee payment: 8 |
|
PLBE | No opposition filed within time limit |
Free format text: ORIGINAL CODE: 0009261 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT |
|
26N | No opposition filed | ||
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: LI Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 19971130 Ref country code: CH Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 19971130 |
|
REG | Reference to a national code |
Ref country code: CH Ref legal event code: PL |
|
REG | Reference to a national code |
Ref country code: GB Ref legal event code: IF02 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: FR Payment date: 20021017 Year of fee payment: 14 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: SE Payment date: 20021018 Year of fee payment: 14 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: NL Payment date: 20021021 Year of fee payment: 14 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: GB Payment date: 20021106 Year of fee payment: 14 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: DE Payment date: 20021202 Year of fee payment: 14 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: ES Payment date: 20021204 Year of fee payment: 14 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: GB Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20031115 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: SE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20031116 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: ES Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20031117 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: NL Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20040601 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: DE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20040602 |
|
EUG | Se: european patent has lapsed | ||
GBPC | Gb: european patent ceased through non-payment of renewal fee |
Effective date: 20031115 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: FR Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20040730 |
|
NLV4 | Nl: lapsed or anulled due to non-payment of the annual fee |
Effective date: 20040601 |
|
REG | Reference to a national code |
Ref country code: FR Ref legal event code: ST |
|
REG | Reference to a national code |
Ref country code: ES Ref legal event code: FD2A Effective date: 20031117 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: IT Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES;WARNING: LAPSES OF ITALIAN PATENTS WITH EFFECTIVE DATE BEFORE 2007 MAY HAVE OCCURRED AT ANY TIME BEFORE 2007. THE CORRECT EFFECTIVE DATE MAY BE DIFFERENT FROM THE ONE RECORDED. Effective date: 20051115 |