EP1326952A1 - Composition a base de polysaccharide anionique pour le soin du linge - Google Patents
Composition a base de polysaccharide anionique pour le soin du lingeInfo
- Publication number
- EP1326952A1 EP1326952A1 EP01978549A EP01978549A EP1326952A1 EP 1326952 A1 EP1326952 A1 EP 1326952A1 EP 01978549 A EP01978549 A EP 01978549A EP 01978549 A EP01978549 A EP 01978549A EP 1326952 A1 EP1326952 A1 EP 1326952A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- anionic polysaccharide
- composition according
- anionic
- dry
- composition
- 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.)
- Granted
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 103
- 229920001586 anionic polysaccharide Polymers 0.000 title claims abstract description 59
- 150000004836 anionic polysaccharides Chemical class 0.000 title claims abstract description 59
- 239000004753 textile Substances 0.000 title claims abstract description 28
- 238000005406 washing Methods 0.000 claims abstract description 45
- 238000009472 formulation Methods 0.000 claims abstract description 44
- 239000003599 detergent Substances 0.000 claims abstract description 39
- 239000000654 additive Substances 0.000 claims abstract description 21
- 229920000742 Cotton Polymers 0.000 claims abstract description 19
- 230000000996 additive effect Effects 0.000 claims abstract description 17
- 239000007787 solid Substances 0.000 claims abstract description 14
- 125000000129 anionic group Chemical group 0.000 claims abstract description 12
- 239000007788 liquid Substances 0.000 claims abstract description 10
- 238000010409 ironing Methods 0.000 claims abstract description 9
- -1 alkyl radical Chemical group 0.000 claims description 48
- 125000004432 carbon atom Chemical group C* 0.000 claims description 25
- 239000000835 fiber Substances 0.000 claims description 16
- 150000003839 salts Chemical class 0.000 claims description 15
- 239000011734 sodium Substances 0.000 claims description 14
- 238000010790 dilution Methods 0.000 claims description 13
- 239000012895 dilution Substances 0.000 claims description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 13
- 229910052799 carbon Inorganic materials 0.000 claims description 10
- 229920000926 Galactomannan Polymers 0.000 claims description 9
- SHZGCJCMOBCMKK-UHFFFAOYSA-N D-mannomethylose Natural products CC1OC(O)C(O)C(O)C1O SHZGCJCMOBCMKK-UHFFFAOYSA-N 0.000 claims description 8
- PNNNRSAQSRJVSB-UHFFFAOYSA-N L-rhamnose Natural products CC(O)C(O)C(O)C(O)C=O PNNNRSAQSRJVSB-UHFFFAOYSA-N 0.000 claims description 8
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 7
- 239000007864 aqueous solution Substances 0.000 claims description 7
- 239000006185 dispersion Substances 0.000 claims description 7
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 7
- 229920001282 polysaccharide Polymers 0.000 claims description 7
- 239000005017 polysaccharide Substances 0.000 claims description 7
- 150000004804 polysaccharides Chemical class 0.000 claims description 7
- 150000003254 radicals Chemical class 0.000 claims description 7
- 229910052708 sodium Inorganic materials 0.000 claims description 7
- 238000006467 substitution reaction Methods 0.000 claims description 7
- 239000004094 surface-active agent Substances 0.000 claims description 7
- 125000000217 alkyl group Chemical group 0.000 claims description 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 6
- 229910052783 alkali metal Inorganic materials 0.000 claims description 5
- 150000001340 alkali metals Chemical class 0.000 claims description 5
- 125000003118 aryl group Chemical group 0.000 claims description 5
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- 238000012986 modification Methods 0.000 claims description 5
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- SHZGCJCMOBCMKK-PQMKYFCFSA-N L-Fucose Natural products C[C@H]1O[C@H](O)[C@@H](O)[C@@H](O)[C@@H]1O SHZGCJCMOBCMKK-PQMKYFCFSA-N 0.000 claims description 4
- SHZGCJCMOBCMKK-DHVFOXMCSA-N L-fucopyranose Chemical compound C[C@@H]1OC(O)[C@@H](O)[C@H](O)[C@@H]1O SHZGCJCMOBCMKK-DHVFOXMCSA-N 0.000 claims description 4
- PNNNRSAQSRJVSB-BXKVDMCESA-N aldehydo-L-rhamnose Chemical compound C[C@H](O)[C@H](O)[C@@H](O)[C@@H](O)C=O PNNNRSAQSRJVSB-BXKVDMCESA-N 0.000 claims description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 4
- SRBFZHDQGSBBOR-UHFFFAOYSA-N beta-D-Pyranose-Lyxose Natural products OC1COC(O)C(O)C1O SRBFZHDQGSBBOR-UHFFFAOYSA-N 0.000 claims description 4
- AEMOLEFTQBMNLQ-UHFFFAOYSA-N beta-D-galactopyranuronic acid Natural products OC1OC(C(O)=O)C(O)C(O)C1O AEMOLEFTQBMNLQ-UHFFFAOYSA-N 0.000 claims description 4
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 4
- 150000002402 hexoses Chemical group 0.000 claims description 4
- 230000007935 neutral effect Effects 0.000 claims description 4
- 239000001301 oxygen Substances 0.000 claims description 4
- 229910052760 oxygen Inorganic materials 0.000 claims description 4
- 239000011343 solid material Substances 0.000 claims description 4
- OMDQUFIYNPYJFM-XKDAHURESA-N (2r,3r,4s,5r,6s)-2-(hydroxymethyl)-6-[[(2r,3s,4r,5s,6r)-4,5,6-trihydroxy-3-[(2s,3s,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]methoxy]oxane-3,4,5-triol Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@@H]1OC[C@@H]1[C@@H](O[C@H]2[C@H]([C@@H](O)[C@H](O)[C@@H](CO)O2)O)[C@H](O)[C@H](O)[C@H](O)O1 OMDQUFIYNPYJFM-XKDAHURESA-N 0.000 claims description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 3
- WQZGKKKJIJFFOK-DHVFOXMCSA-N L-galactose Chemical compound OC[C@@H]1OC(O)[C@@H](O)[C@H](O)[C@@H]1O WQZGKKKJIJFFOK-DHVFOXMCSA-N 0.000 claims description 3
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 3
- 150000001408 amides Chemical class 0.000 claims description 3
- 125000002057 carboxymethyl group Chemical group [H]OC(=O)C([H])([H])[*] 0.000 claims description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 3
- 238000000034 method Methods 0.000 claims description 3
- 125000001731 2-cyanoethyl group Chemical group [H]C([H])(*)C([H])([H])C#N 0.000 claims description 2
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 claims description 2
- AEMOLEFTQBMNLQ-DTEWXJGMSA-N D-Galacturonic acid Natural products O[C@@H]1O[C@H](C(O)=O)[C@H](O)[C@H](O)[C@H]1O AEMOLEFTQBMNLQ-DTEWXJGMSA-N 0.000 claims description 2
- SRBFZHDQGSBBOR-IOVATXLUSA-N D-xylopyranose Chemical compound O[C@@H]1COC(O)[C@H](O)[C@H]1O SRBFZHDQGSBBOR-IOVATXLUSA-N 0.000 claims description 2
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 claims description 2
- 229920002324 Galactoglucomannan Polymers 0.000 claims description 2
- SRBFZHDQGSBBOR-OWMBCFKOSA-N L-ribopyranose Chemical compound O[C@H]1COC(O)[C@@H](O)[C@H]1O SRBFZHDQGSBBOR-OWMBCFKOSA-N 0.000 claims description 2
- 229910019142 PO4 Inorganic materials 0.000 claims description 2
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical group OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 claims description 2
- 229920002305 Schizophyllan Polymers 0.000 claims description 2
- 229920002310 Welan gum Polymers 0.000 claims description 2
- IAJILQKETJEXLJ-RSJOWCBRSA-N aldehydo-D-galacturonic acid Chemical compound O=C[C@H](O)[C@@H](O)[C@@H](O)[C@H](O)C(O)=O IAJILQKETJEXLJ-RSJOWCBRSA-N 0.000 claims description 2
- GZCGUPFRVQAUEE-KVTDHHQDSA-N aldehydo-D-mannose Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)C=O GZCGUPFRVQAUEE-KVTDHHQDSA-N 0.000 claims description 2
- AEMOLEFTQBMNLQ-WAXACMCWSA-N alpha-D-glucuronic acid Chemical compound O[C@H]1O[C@H](C(O)=O)[C@@H](O)[C@H](O)[C@H]1O AEMOLEFTQBMNLQ-WAXACMCWSA-N 0.000 claims description 2
- PYMYPHUHKUWMLA-UHFFFAOYSA-N arabinose Natural products OCC(O)C(O)C(O)C=O PYMYPHUHKUWMLA-UHFFFAOYSA-N 0.000 claims description 2
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 2
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 claims description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- 150000007942 carboxylates Chemical class 0.000 claims description 2
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 2
- AEMOLEFTQBMNLQ-YBSDWZGDSA-N d-mannuronic acid Chemical compound O[C@@H]1O[C@@H](C(O)=O)[C@H](O)[C@@H](O)[C@H]1O AEMOLEFTQBMNLQ-YBSDWZGDSA-N 0.000 claims description 2
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 2
- 150000002148 esters Chemical class 0.000 claims description 2
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 2
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 2
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- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 claims description 2
- 229920001285 xanthan gum Polymers 0.000 claims description 2
- 244000007835 Cyamopsis tetragonoloba Species 0.000 claims 2
- FEBUJFMRSBAMES-UHFFFAOYSA-N 2-[(2-{[3,5-dihydroxy-2-(hydroxymethyl)-6-phosphanyloxan-4-yl]oxy}-3,5-dihydroxy-6-({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-4-yl)oxy]-3,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl phosphinite Chemical compound OC1C(O)C(O)C(CO)OC1OCC1C(O)C(OC2C(C(OP)C(O)C(CO)O2)O)C(O)C(OC2C(C(CO)OC(P)C2O)O)O1 FEBUJFMRSBAMES-UHFFFAOYSA-N 0.000 claims 1
- GZCGUPFRVQAUEE-DPYQTVNSSA-N aldehydo-L-galactose Chemical group OC[C@H](O)[C@@H](O)[C@@H](O)[C@H](O)C=O GZCGUPFRVQAUEE-DPYQTVNSSA-N 0.000 claims 1
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- IBDSNZLUHYKHQP-UHFFFAOYSA-N sodium;3-oxidodioxaborirane;tetrahydrate Chemical compound O.O.O.O.[Na+].[O-]B1OO1 IBDSNZLUHYKHQP-UHFFFAOYSA-N 0.000 description 1
- NWPMTMCXJZTLSO-UHFFFAOYSA-M sodium;4-acetyloxybenzenesulfonate Chemical compound [Na+].CC(=O)OC1=CC=C(S([O-])(=O)=O)C=C1 NWPMTMCXJZTLSO-UHFFFAOYSA-M 0.000 description 1
- MWNQXXOSWHCCOZ-UHFFFAOYSA-L sodium;oxido carbonate Chemical compound [Na+].[O-]OC([O-])=O MWNQXXOSWHCCOZ-UHFFFAOYSA-L 0.000 description 1
- YKLJGMBLPUQQOI-UHFFFAOYSA-M sodium;oxidooxy(oxo)borane Chemical compound [Na+].[O-]OB=O YKLJGMBLPUQQOI-UHFFFAOYSA-M 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- PJANXHGTPQOBST-UHFFFAOYSA-N stilbene Chemical class C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
- 238000006277 sulfonation reaction Methods 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- 229940095064 tartrate Drugs 0.000 description 1
- FRPJTGXMTIIFIT-UHFFFAOYSA-N tetraacetylethylenediamine Chemical compound CC(=O)C(N)(C(C)=O)C(N)(C(C)=O)C(C)=O FRPJTGXMTIIFIT-UHFFFAOYSA-N 0.000 description 1
- 150000004685 tetrahydrates Chemical class 0.000 description 1
- 229930192474 thiophene Natural products 0.000 description 1
- 150000003577 thiophenes Chemical class 0.000 description 1
- GTZCVFVGUGFEME-UHFFFAOYSA-N trans-aconitic acid Natural products OC(=O)CC(C(O)=O)=CC(O)=O GTZCVFVGUGFEME-UHFFFAOYSA-N 0.000 description 1
- JSPLKZUTYZBBKA-UHFFFAOYSA-N trioxidane Chemical class OOO JSPLKZUTYZBBKA-UHFFFAOYSA-N 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 1
- 239000003643 water by type Substances 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 239000002888 zwitterionic surfactant Substances 0.000 description 1
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
- C11D3/16—Organic compounds
- C11D3/20—Organic compounds containing oxygen
- C11D3/22—Carbohydrates or derivatives thereof
- C11D3/222—Natural or synthetic polysaccharides, e.g. cellulose, starch, gum, alginic acid or cyclodextrin
- C11D3/226—Natural or synthetic polysaccharides, e.g. cellulose, starch, gum, alginic acid or cyclodextrin esterified
-
- 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
- C11D3/20—Organic compounds containing oxygen
- C11D3/22—Carbohydrates or derivatives thereof
- C11D3/222—Natural or synthetic polysaccharides, e.g. cellulose, starch, gum, alginic acid or cyclodextrin
-
- 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
- C11D3/20—Organic compounds containing oxygen
- C11D3/22—Carbohydrates or derivatives thereof
- C11D3/222—Natural or synthetic polysaccharides, e.g. cellulose, starch, gum, alginic acid or cyclodextrin
- C11D3/225—Natural or synthetic polysaccharides, e.g. cellulose, starch, gum, alginic acid or cyclodextrin etherified, e.g. CMC
-
- 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
- C11D3/20—Organic compounds containing oxygen
- C11D3/22—Carbohydrates or derivatives thereof
- C11D3/222—Natural or synthetic polysaccharides, e.g. cellulose, starch, gum, alginic acid or cyclodextrin
- C11D3/227—Natural or synthetic polysaccharides, e.g. cellulose, starch, gum, alginic acid or cyclodextrin with nitrogen-containing groups
Definitions
- the subject of the present invention is a composition comprising an anionic polysaccharide for the care of articles made of textile fibers ("textile care"), based on cotton in particular, colored in particular.
- Care for textile fiber articles, linen in particular, means the protection of the latter against physical or chemical degradation phenomena, in particular the protection of the colors of the colored articles, and / or the contribution to those -these benefits such as softening and / or anti-creasing properties.
- Machine washing of the linen leads to physical and chemical degradation of the fibers and especially of the cotton fibers.
- the alkalinity delivered by detergents as well as certain specific compounds such as oxidizing substances (perborate, percarbonate) or certain enzymes can be at the origin of the chemical degradation of cotton fibers. But it is generally the conjunction of chemical and mechanical actions that leads to fiber degradation.
- the mechanical action is produced during washing, rinsing, spinning or drying, when the latter takes place in a dryer.
- This degradation of the fibers leads to the formation of fibrils on the surface of the textile which ultimately give a loss of luster in colored textiles. This degradation also induces a reduction in the resistance of the textile which in the extreme can lead to a tearing of the fabrics.
- This degradation of the textiles can be quantitatively evaluated either by a loss of the colors of the colored textiles or by a reduction in the breaking energy of the textile. It is generally necessary to carry out 10 to 20 cumulative machine washes to perceive this type of degradation. Cleaning in a washing machine machine which systematically includes a spinning operation also leads to a crumpled cloth which is accentuated during drying, in particular by the formation of inter-fiber hydrogen bonds. An ironing operation is therefore necessary to obtain a presentable appearance of the laundry. In order to reduce the degradation of the fibers during washing or rinsing, the suppliers of chemical products or detergents have resorted to modifications of detergent formulas or to the use of certain specific additives.
- compositions for the treatment of articles of textile fibers in particular based on cotton, colored in particular, of certain anionic polysaccharides of high molecular mass which are soluble under the conditions of use ("working conditions” ) in an aqueous or moist medium of said compositions, made it possible to avoid the degradation of these articles, made it possible to protect the colors and / or provided them with anti-crease and / or softening properties.
- Such compositions may in particular be compositions for washing and / or rinsing and / or softening the laundry, for detaching the laundry before washing ("prespotting"), for drying wet laundry in a dryer or for ironing clothes.
- a first object of the invention consists of a composition for the care of articles made of textile fibers ("fabric care"), characterized in that it comprises at least one anionic polysaccharide with a molar mass by weight greater than 250,000, preferably greater than 500,000, whose native skeleton is a polysaccharide formed
- * and of branches comprising at least one neutral or anionic anhydropentose and / or anhydrohexose unit, the anhydrohexose and / or anhydropentose units of said anionic polysaccharide being substituted or modified by at least one anionic or anionizable group at the pH of use of said composition, the degree DSi substitution or modification of anhydrohexose and / or anhydropentose units by said anionic or anionizable group (s) ranging from 0.1 to less than 3, preferably from 0.2 to 2.5.
- the molar mass by weight of said anionic polysaccharides can range up to 2,000,000.
- the molar mass by weight Mw of said anionic polysaccharides can be measured by size exclusion chromatography. The measurement is carried out in water at pH 9-10 containing 0.1 M of LiCI and 2/10000 of N 3 Na.
- the molar mass by weight Mw is established in a known manner directly via the light scattering values.
- the degree of substitution or modification DSi corresponds to the average number of hydroxyl functions of the anhydrohexose and / or anhydropentose units substituted or modified by said anionic or anionizable group (s), per anhydrohexose and / or anhydropentose unit.
- Said ionic or ionizable groups are linked to the carbon atoms of the sugar skeleton either directly or via -O- bonds.
- said anionic polysaccharide can also have at least one nonionic group.
- Said nonionic groups are linked to the carbon atoms of the sugar skeleton either directly or via -O- bonds.
- the presence of such groups is expressed in number of moles of substitution MS, that is to say in average number of moles of precursor of said nonionic substituent having reacted by anhydrohexose and / or anhydropentose unit. If said precursor is not capable of forming new reactive hydroxyl groups (alkylation precursor for example), the degree of substitution or modification by all of the anionic or anionizable and nonionic groups is less than 3 by definition .
- the number of moles of substitution MS is theoretically not limited; it can for example go up to 6, preferably up to 2.
- anionic or anionizable groups mention may be made of those containing one or more carboxylate, sulfonate, sulfate, phosphate, phosphonate functions, etc.
- R is a hydrogen atom or an alkyl radical containing from 1 to 4 carbon atoms
- x is an integer ranging from 0 to 5
- y is an integer ranging from 0 to 5
- M represents an alkali metal.
- R is a hydrogen atom or an alkyl radical containing from 1 to 4 carbon atoms, x is an integer ranging from 0 to 5, R 1 represents:. a hydrogen atom
- a radical - (CH 2 ) y -CONHR 2 R 2 representing an alkyl, aryl or arylalkyl radical containing from 1 to 22 carbon atoms, and y is an integer ranging from 0 to 5 • -CO-NH-R 1
- R 1 having the definition given above, linked to a carbon atom of the sugar skeleton via a bond
- the hexose units (similar or different) of the main chain of the native skeleton can be D-glucose, D- or L-galactose, D-mannose, D- or L-fucose, L-rhamnose ...
- the neutral or anionic pentose and / or hexose units (similar or different) of the ramifications of the native skeleton can be D-xylose ..., L- or D-arabinose, D-glucose, D- or L-galactose, D -mannose,
- a native skeleton mention may be made of galactomannans, galactoglucomannans, xyloglucans, xanthan gums, scleroglucans, succinoglycans, rhamsans, welan gums ...
- the native skeleton is a galactomannan.
- Galactomannans are macromolecules comprising a main chain of D-mannopyranose units linked in position ⁇ (1 -4) substituted by D-galactopyranose units in position ⁇ (1-6).
- guar carob, tara gums.
- the native skeleton is a guar gum.
- Guar gums have a mannose / galactose ratio of 2.
- the anionic polysaccharides according to the invention can be obtained in a known manner.
- anionic polysaccharides there may be mentioned:
- a second object of the invention consists in a process for caring for articles made of textile fibers, by treatment of the latter with a composition, in an aqueous or humid medium, comprising at least one anionic polysaccharide according to the invention.
- a third subject of the invention consists in the use, in a composition for the treatment of articles of textile fibers in an aqueous or humid medium, of at least one anionic polysaccharide according to the invention, as a care agent for textile articles.
- compositions and the conditions of use (or treatment) can be multiple.
- Said composition can be in the form of a solid (powder, granules, tablets, etc.) or a dispersion or a concentrated aqueous solution, brought into contact with the articles to be treated, after dilution in water. ; * in the form of a dispersion or a concentrated aqueous solution previously deposited on the dry articles to be treated before dilution in water; * in the form of a dispersion or an aqueous solution to be deposited directly on the dry articles to be treated without dilution or of a solid support (stick) comprising said anionic polysaccharide, to be applied directly to the dry articles to be treated; * in the form of an insoluble solid support comprising said anionic polysaccharide brought into contact directly with the articles to be treated in the wet state.
- composition of the invention can be:
- liquid rinsing and / or softening formulation capable of directly forming, by dilution, a rinsing and / or softening bath;
- drying additive a solid material, in particular textile, comprising said anionic polysaccharide, intended to be brought into contact with wet articles in a dryer (said solid material is hereinafter called "drying additive");
- washing additive intended to be deposited on dry articles prior to a washing operation using a detergent formulation containing or not containing said anionic polysaccharide (said additive is called below " washing additive ").
- composition of the invention is particularly well suited to the care of linen, in particular cotton-based, in particular containing at least 35% cotton. It is particularly suitable for the care of colored linen.
- anionic polysaccharides according to the invention are soluble under the conditions of use ("working conditions") in aqueous or wet medium of said composition.
- Said anionic polysaccharides are considered to be soluble when more than 50%, preferably more than 70% of their weight, are soluble in the aqueous or moist medium of use of the composition of the invention, that is to say in particular in the temperature and pH conditions of said medium.
- the pH of use of the composition of the invention can range from approximately 2 to approximately 12, depending on the desired use.
- the pH of the detergent bath is generally of the order of 7 to 11, preferably of 8 to 10.5;
- the pH of the rinsing and / or softening bath is generally of the order of 2 to 8;
- a drying additive the pH to be considered is that of residual water, which can be of the order of 2 to 9;
- the pH of said formulation is generally of the order of 5 to 9;
- the pH to be considered is that of the pH of the washing bath of the following washing operation, namely of the order of 7 to 11, preferably from 8 to 10.5.
- the amount of anionic polysaccharide present in the care composition according to the invention can range from 0.05 to 10% on a dry basis of the weight of said composition on a dry basis, depending on the desired application.
- anionic polysaccharide (PA) can be used as follows:
- compositions may contain at least one surfactant and / or a detergency and / or rinsing and / or softening additive for articles made of textile fibers and / or a solid support (textile in particular) of said anionic polysaccharide.
- surfactant and / or a detergency and / or rinsing and / or softening additive for articles made of textile fibers and / or a solid support (textile in particular) of said anionic polysaccharide.
- solid support textile in particular
- the detergent formulation may include surfactants in an amount corresponding to about 3 to 40% by weight based on the detergent formulation, surfactants such as anionic surfactants.
- methyl ester sulfonates whose radicals R is C ⁇ 4 -C- ⁇ 6 ; . alkyl sulphates of formula ROSO 3 M, where R represents an alkyl or hydroxyalkyl radical, C 5 -C 24, preferably CI O -C- IS, M representing a hydrogen atom or a cation with the same definition as above , as well as their ethoxylenated (OE) and or propoxylenated (OP) derivatives, having on average from 0.5 to 30 units, preferably from 0.5 to 10 OE and / or OP units; .
- R represents an alkyl or hydroxyalkyl radical, C 5 -C 24, preferably CI O -C- IS
- M representing a hydrogen atom or a cation with the same definition as above , as well as their ethoxylenated (OE) and or propoxylenated (OP) derivatives, having on average from 0.5 to 30 units, preferably from 0.5 to 10 OE and
- RCONHR'OSO 3 M where R represents an alkyl radical in C 2 -C 22 , preferably in C 6 -C 2 o, R 'an alkyl radical in C 2 -C 3 , M representing an atom d hydrogen or a cation with the same definition as above, as well as their ethoxylenated (OE) and / or propoxylenated derivatives
- OP having on average from 0.5 to 60 OE and / or OP units; . salts of C 8 -C 24 saturated or unsaturated fatty acids, preferably C ⁇ 4 -C 20 , C 9 -C 20 alkylbenzenesulfonates, C 8 -C 22 primary or secondary alkylsulfonates, alkylglycerol sulfonates, sulfonated polycarboxylic acids described in GB-A-1 082 179, paraffin sulfonates, N-acyl N-alkyltaurates, alkylphosphates, isethionates, alkylsuccinamates, alkylsulfosuccinates, monoesters or diesters of sulfosuccinates, N- acyl sarcosinates, alkyl glycoside sulfates, polyethoxycarboxylates; the cation being an alkali metal (sodium, potassium, lithium),
- 25 oxyalkylene units by way of example, mention may be made of the Triton X-45, X-114, X-100 or X-102 sold by Rohm & Haas Cy. ; glucosamide, glucamide, glycerolamide; .
- polyoxyalkylenated C 8 -C 22 aliphatic alcohols containing from 1 to 25 oxyalkylene units oxyethylene, oxypropylene
- TERGITOL 15-S-9 TERGITOL 24-L-6 NMW sold by Union Carbide Corp.
- NEODOL 45-9 NEODOL 23-65, NEODOL 45-7
- NEODOL 45-4 marketed by Shell Chemical Cy.
- KYRO EOB marketed by The Procter & Gamble Cy.
- amine oxides such as alkyl oxides C ⁇ oCi s dimethylamines, alkoxy oxides C 8 -C 22 ethyl dihydroxy ethylamines; . the alkylpolyglycosides described in US-A-4,565,647; amides of C 8 -C 20 fatty acids; ethoxylated fatty acids; ethoxylated fatty amides; ethoxylated amines.
- Amphoteric and zwitterionic surfactants such as alkyl oxides C ⁇ oCi s dimethylamines, alkoxy oxides C 8 -C 22 ethyl dihydroxy ethylamines; . the alkylpolyglycosides described in US-A-4,565,647; amides of C 8 -C 20 fatty acids; ethoxylated fatty acids; ethoxylated fatty amides; ethoxylated amines
- alkyldimethylbetaines alkylamidopropyldimethylbetaines, alkyltrimethylsulfobetaines, condensation products of fatty acids and protein hydriysates; . alkylamphoacetates or alkylamphodiacetates in which the alkyl group contains from 6 to 20 carbon atoms.
- Detergency builders improving the properties of surfactants can be used in amounts corresponding to about 5-50%, preferably about 5-30% by weight for liquid detergent formulas or about 10 -80%, preferably 15-50% by weight for detergent formulas in powders, detergency builders such as: Inorganic detergency builders. polyphosphates (tripolyphosphates, pyrophosphates, orthophosphates, hexametaphosphates) of alkali metals, ammonium or alkanolamines. tetraborates or borate precursors; .
- silicates in particular those having a SiO 2 / Na 2 O ratio of the order of 1.6 / 1 to 3.2 / 1 and the lamellar silicates described in US-A-4,664,839; . alkali or alkaline earth carbonates (bicarbonates, sesquicarbonates); . cogranules of hydrated alkali metal silicates and alkali metal carbonates (sodium or potassium) rich in silicon atoms in Q2 or Q3 form, described in EP-A-488 868; .
- the detergent formulation may further comprise at least one oxygen-releasing bleaching agent comprising a per-compound, preferably a persalt.
- Said bleaching agent can be present in an amount corresponding to approximately 1 to 30%, preferably from 4 to 20% by weight relative to the detergent formulation.
- per-compounds capable of being used as bleaching agents mention should be made in particular of perborates such as sodium perborate monohydrate or tetrahydrate; peroxygenated compounds such as sodium carbonate peroxyhydrate, pyrophosphate peroxyhydrate, urea peroxyhydrate, sodium peroxide, sodium persulfate.
- perborates such as sodium perborate monohydrate or tetrahydrate
- peroxygenated compounds such as sodium carbonate peroxyhydrate, pyrophosphate peroxyhydrate, urea peroxyhydrate, sodium peroxide, sodium persulfate.
- Preferred bleaching agents are sodium perborate, mono- or tetrahydrate and / or sodium carbonate peroxyhydrate.
- Said agents are generally combined with a bleach activator generating in situ in the washing medium, a peroxycarboxylic acid, in an amount corresponding to approximately 0.1 to 12%, preferably from 0.5 to 8% by weight relative to the detergent formulation.
- a bleach activator generating in situ in the washing medium, a peroxycarboxylic acid, in an amount corresponding to approximately 0.1 to 12%, preferably from 0.5 to 8% by weight relative to the detergent formulation.
- these activators mention may be made of tetraacetylethylenediamine, tetraacetylmethylenediamine, sodium tetraacetylglycoluryl, sodium p-acetoxybenzenesulfonate, pentaacetylglucose, octaacetyllactose. Mention may also be made of non-oxygenated bleaching agents, acting by photoactivation in the presence of oxygen, agents such as sulfonated aluminum and / or zinc phthalocyan
- the detergent formulation may further comprise anti-fouling agents ("soil release”), anti-redeposition, chelating agents, dispersants, fluorescence, foam suppressants, softeners, enzymes and other various additives.
- anti-fouling agents oil release
- anti-redeposition chelating agents
- dispersants fluorescence, foam suppressants, softeners, enzymes and other various additives.
- They can be used in amounts of approximately 0.01-10%, preferably approximately 0.1-5%, and more preferably of the order of 0.2-3% by weight.
- agents such as:. cellulose derivatives such as cellulose hydroxyethers, methylcellulose, ethylcellulose, hydroxypropyl methylcellulose, hydroxybutyl methylcellulose; . polyvinyl esters grafted on polyalkylene trunks such as polyvinylacetates grafted on polyoxyethylene trunks (EP-A-219 048); . polyvinyl alcohols;
- polyoxyethylene terephthalate of the order of 1/10 to 10/1, preferably of the order of 1/1 to 9/1, the polyoxyethylene terephthalates having polyoxyethylene units having a molecular weight of the order from 300 to 5,000, preferably in the range of 600 to 5,000 (US-A-3,959,230, US-A-3,893,929, US-A-4,116,896, US-A-4,702,857, US-A-4,770,666);
- polyester oligomers obtained by sulfonation of an oligomer derived from ethoxylated allyl alcohol, dimethyl terephthalate and 1,2-propylene diol, having from 1 to 4 sulfonated groups (US Pat. No. 4,968,451); . polyester copolymers based on propylene terephthalate and polyoxyethylene terephthalate units and terminated with ethyl, methyl units
- polyester oligomers terminated by alkylpolyethoxy groups (US-A-4,702,857) or anionic sulfopolyethoxy groups (US-A-4,721,580), sulfoaroyles (US-A-4,877 896);
- sulfonated polyester copolymers derived from terephthalic, isophthalic and sulfoisophthalic acid, anhydride or diester and a diol FR-A-2 720 399.
- Anti-redeposition agents FR-A-2 720 399.
- agents such as:. ethoxylated monoamines or polyamines, polymers of ethoxylated amines (US-A-4,597,898, EP-A-11,984); . carboxymethylcellulose;
- sulfonated polyester oligomers obtained by condensation of isophthalic acid, dimethyl sulfosuccinate and diethylene glycol (FR-A-
- the iron and magnesium chelating agents can be present in amounts of the order of 0.1 -10%, preferably of the order of 0.1-3% by weight.
- aminocarboxylates such as ethylenediaminetetraacetates, hydroxyethylethylenediaminetriacetates, nitrilotriacetates;
- aminophosphonates such as nitrilotris- (methylenephosphonates); polyfunctional aromatic compounds such as dihydroxy-disulfobenzenes.
- Polymeric dispersing agents They can be present in an amount of the order of 0.1-7% by weight, to control the hardness of calcium and magnesium, agents such as.
- the water-soluble salts of polycarboxylic acids of molecular mass of the order of 2,000 to 100,000 obtained by polymerization or copolymerization of ethylenically unsaturated carboxylic acids such as acrylic acid, maleic acid or anhydride, fumaric acid, itaconic acid, aconitic acid , mesaconic acid, citraconic acid, methylenemalonic acid, and more particularly polyacrylates of molecular weight of the order of 2,000 to 10,000 (US-A-3,308,067), copolymers arylic acid and maleic anhydride with a molecular mass of the order of 5,000 to 75,000 (EP-A-66,915),.
- carboxylic acids such as acrylic acid, maleic acid or anhydride, fumaric acid, itaconic acid, aconitic acid , mesaconic acid, citraconic acid, methylenemalonic acid, and more particularly polyacrylates of molecular weight of the order of 2,000 to 10,000 (US-A
- Fluorescent agents (brighteners), They may be present in an amount of approximately 0.05-1.2% by weight, agents such as: derivatives of stilbene, pyrazoline, coumarin, fumaric acid, cinnamic acid, azoles, methinecyanins, thiophenes ... ("The production and application of fluorescent brightening agents" - M. Zahradnik, published by John Wiley & Sons, New York -1982). Foam suppressants.
- agents such as:
- Enzymes can be present in amounts of about 0.5-10% by weight, agents such as clays. Enzymes They can be present in an amount of up to 5 mg by weight, preferably of the order of 0.05-3 mg of active enzyme / g of detergent formulation, enzymes such as:
- proteases amylases, lipases, cellulases, peroxidases (US-A-3,553,139, US-A-4,101,457, US-A-4,507,219, US-A-4,261,868).
- a second embodiment of the care composition of the invention consists of an aqueous liquid formulation for rinsing and / or softening the linen.
- anionic polysaccharide Besides the anionic polysaccharide, other constituents of the type may be present.
- cationic surfactants triethanolamine diester quaternized by dimethylsulfate, N-methylimidazoline tallow methyl sulfate ester, dialkyldimethylammonium chloride, alkylbenzyldimethylammonium chloride, methyl and alkylimidazolinium sulfate, methyl and methyl bis bis ( alkylamidoethyl) -2 hydroxyethylammonium ”) in an amount which can range from 3 to 50%, preferably from 4 to 30% of said formulation optionally combined with nonionic surfactants (ethoxylated fatty alcohols, ethoxylated alkylphenols ...) in an amount which can go up to 3%;
- alcohols methanol, ethanol, propanol, isopropanol, ethylene glycol, glycerin
- foam limiters in particular alcohols (methanol, ethanol, propanol, isopropanol, ethylene glycol, glycerin) - foam limiters.
- a third embodiment of the care composition of the invention consists of a laundry drying additive in an appropriate drying machine.
- Said additive comprises a flexible solid support constituted for example by a strip of woven or nonwoven fabric, a sheet of cellulose, impregnated with said anionic polysaccharide; said additive is introduced on drying in the damp linen to be dried at a temperature of the order of 50 to 80 ° C for 10 to
- a fourth embodiment of the care composition of the invention consists of an ironing formulation which can be sprayed directly onto the dry linen before the ironing operation.
- Said formulation may also contain polymers based on silicone (from 0.2 to 5%), nonionic (from 0.5 to 5%) or anionic (from 0.5 to 5%) surfactants, perfumes (0.1 to 3%), cellulose derivatives (0.1 to 3%) such as starch; spraying said formulation on the linen makes it easier to iron and limit wrinkling of the linen when worn.
- a fifth embodiment of the care composition of the invention consists of a washing additive ("prespotter”) in the form of an aqueous solution or dispersion or a solid (stick) .
- anionic polysaccharide may be present other constituents of the type
- Aliphatic hydrocarbons in an amount which can range from 5% to 20% of the weight of the composition.
- the anionic polysaccharide used in the following examples is a carboxymethyl guar having a degree of substitution of 1.6 and a molar mass by weight of 1,400,000 determined as follows by size exclusion chromatography.
- the measurement is carried out in water at pH 9-10 containing 0.1 M of LiCI and 2/10000 of N 3 Na.
- the characteristics of the device are as follows: - Chromatographic columns: 3 columns Shodex SB806HQ 30cm, 5 ⁇ m
- a washing operation is carried out in a laboratory apparatus
- the device simulates the mechanical and thermal effects of washing machines of the American type with pulsator, but thanks to the presence of 6 washing pots, it allows to carry out series of simultaneous tests with an appreciable saving of time.
- test pieces are then crumpled under a 3kg press for 20 seconds, then allowed to dry vertically overnight.
- a digital color photograph of the dry specimens is then produced, which is then transformed into 256 levels of gray (gray scale from 0 to 255).
- ⁇ i corresponds to the standard deviation obtained with the detergent formulation not containing an anionic polysaccharide.
- ⁇ 2 corresponds to the standard deviation obtained with the detergent formulation containing the anionic polysaccharide.
- Washing conditions Washing temperature 40 ° C Duration: about 67 min
- L * 0_ for a black test tube a * places the color in a range from green to red. a *> 0 the color turns to red. a * ⁇ 0 the color draws on green b * places the color in a range going from yellow to blue. b * > 0 the color turns to yellow. b * ⁇ 0 the color turns to blue.
- the performance of the polysaccharide relative to the reference is measured as the difference in ⁇ E * between the formulas without and with polysaccharide.
- the cumulative color loss is calculated as the sum of the color losses of the colored fabrics.
- a detergent formulation (F) is prepared by adding 1 part of anionic polysaccharide to 100 parts of composition (C) below
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- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Emergency Medicine (AREA)
- Engineering & Computer Science (AREA)
- Molecular Biology (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Detergent Compositions (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Cosmetics (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
Description
Claims
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR0013334 | 2000-10-18 | ||
| FR0013334A FR2815355B1 (fr) | 2000-10-18 | 2000-10-18 | Composition a base de polysaccharide anionique pour le soin du linge |
| PCT/FR2001/003210 WO2002033034A1 (fr) | 2000-10-18 | 2001-10-17 | Composition a base de polysaccharide anionique pour le soin du linge |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EP1326952A1 true EP1326952A1 (fr) | 2003-07-16 |
| EP1326952B1 EP1326952B1 (fr) | 2008-01-02 |
Family
ID=8855465
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP01978549A Expired - Lifetime EP1326952B1 (fr) | 2000-10-18 | 2001-10-17 | Composition a base de polysaccharide anionique pour le soin du linge |
Country Status (10)
| Country | Link |
|---|---|
| US (4) | US20040107505A1 (fr) |
| EP (1) | EP1326952B1 (fr) |
| JP (1) | JP2004511681A (fr) |
| AT (1) | ATE382672T1 (fr) |
| AU (1) | AU2002210655A1 (fr) |
| BR (1) | BR0114624A (fr) |
| CA (1) | CA2426695C (fr) |
| DE (1) | DE60132225T2 (fr) |
| FR (1) | FR2815355B1 (fr) |
| WO (1) | WO2002033034A1 (fr) |
Families Citing this family (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2820747B1 (fr) * | 2001-02-15 | 2005-10-07 | Rhodia Chimie Sa | Composition a base de polysaccharide non-ionique pour le soin des articles en fibres textiles |
| US20080234224A1 (en) * | 2004-03-31 | 2008-09-25 | Motoaki Kamachi | External Preparation For Skin |
| US20060189232A1 (en) * | 2005-02-23 | 2006-08-24 | No-Burn Investments, L.L.C. | Fire retarding, stain and/or mold protecting composition |
| GB0508883D0 (en) * | 2005-04-29 | 2005-06-08 | Unilever Plc | Polymers for laundry applications |
| WO2011017223A1 (fr) | 2009-07-31 | 2011-02-10 | Akzo Nobel N.V. | Compositions de copolymère hybride pour des applications de soin personnel |
| NO20073834L (no) | 2006-07-21 | 2008-01-22 | Akzo Nobel Chemicals Int Bv | Sulfonerte podede kopolymerer |
| EP1997874A1 (fr) * | 2007-05-25 | 2008-12-03 | JohnsonDiversey, Inc. | Système de nettoyage d'articles contenant du polysaccharide |
| US8796196B2 (en) * | 2010-02-26 | 2014-08-05 | Hercules Incorporated | Polysaccharide products with improved performance and clarity in surfactant-based aqueous formulations and process for preparation |
| US9561166B2 (en) | 2010-02-26 | 2017-02-07 | Hercules Incorporated | Polysaccharide products with improved performance and clarity in phosphate ester surfactant-based aqueous formulations and process for preparation |
| WO2012166161A1 (fr) | 2011-06-03 | 2012-12-06 | Hewlett-Packard Development Company, L.P. | Systèmes permettant d'effacer une encre d'un support |
| WO2012166147A1 (fr) * | 2011-06-03 | 2012-12-06 | Hewlett-Packard Development Company, L.P. | Fluide d'effacement |
| US8679366B2 (en) | 2011-08-05 | 2014-03-25 | Ecolab Usa Inc. | Cleaning composition containing a polysaccharide graft polymer composition and methods of controlling hard water scale |
| US8841246B2 (en) | 2011-08-05 | 2014-09-23 | Ecolab Usa Inc. | Cleaning composition containing a polysaccharide hybrid polymer composition and methods of improving drainage |
| US8636918B2 (en) | 2011-08-05 | 2014-01-28 | Ecolab Usa Inc. | Cleaning composition containing a polysaccharide hybrid polymer composition and methods of controlling hard water scale |
| US8853144B2 (en) | 2011-08-05 | 2014-10-07 | Ecolab Usa Inc. | Cleaning composition containing a polysaccharide graft polymer composition and methods of improving drainage |
| JP2014532791A (ja) | 2011-11-04 | 2014-12-08 | アクゾ ノーベル ケミカルズ インターナショナル ベスローテン フエンノートシャップAkzo Nobel Chemicals International B.V. | ハイブリッド樹状コポリマー、その組成物及びそれを製造する方法 |
| US9051406B2 (en) | 2011-11-04 | 2015-06-09 | Akzo Nobel Chemicals International B.V. | Graft dendrite copolymers, and methods for producing the same |
| US8945314B2 (en) | 2012-07-30 | 2015-02-03 | Ecolab Usa Inc. | Biodegradable stability binding agent for a solid detergent |
| US9365805B2 (en) | 2014-05-15 | 2016-06-14 | Ecolab Usa Inc. | Bio-based pot and pan pre-soak |
| GB201616657D0 (en) | 2016-09-30 | 2016-11-16 | Innospec Ltd | Methods, compositions and uses relating thereto |
| WO2025118258A1 (fr) * | 2023-12-08 | 2025-06-12 | Dow Global Technologies Llc | Détergent pour lave-vaisselle à base de gomme de guar carboxyalkyle hydroxyalkyle |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3133317A1 (de) * | 1981-08-22 | 1983-03-10 | Kali-Chemie Ag, 3000 Hannover | Verfahren zur herstellung von zeolith-agglomeraten |
| JPS59128324A (ja) * | 1983-01-06 | 1984-07-24 | Mitsubishi Acetate Co Ltd | 防菌性粒状物及びその製造方法 |
| DE3709698C1 (de) * | 1987-03-25 | 1988-10-27 | Diamalt Ag | Schlichtemittel |
| DE69200846T2 (de) * | 1991-03-19 | 1995-05-18 | Novonordisk As | Entfernung von druckpasten-verdicker und überschuss an farbstoff nach textildruck. |
| DE4321016A1 (de) * | 1993-06-24 | 1995-01-05 | Henkel Kgaa | Carboxymethyliertes Guargalaktomannan als Schlichtemittel |
| JP2837360B2 (ja) * | 1994-08-03 | 1998-12-16 | 日清製油株式会社 | 洗浄剤組成物 |
| DK0934343T3 (da) * | 1996-10-25 | 2003-04-28 | Rhodia | Afledt guargummisammensætning indbefattende non-ioniske og kationiske grupper, der udviser enestående egenskaber til klaring af opløsninger til brug som rengøringsmidler |
| FR2818983B1 (fr) * | 2000-12-28 | 2005-09-09 | Rhodia Chimie Sa | Polysaccharide amphotere et son utilisation pour le soin des articles en fibres textiles |
-
2000
- 2000-10-18 FR FR0013334A patent/FR2815355B1/fr not_active Expired - Fee Related
-
2001
- 2001-10-17 AU AU2002210655A patent/AU2002210655A1/en not_active Abandoned
- 2001-10-17 EP EP01978549A patent/EP1326952B1/fr not_active Expired - Lifetime
- 2001-10-17 JP JP2002536404A patent/JP2004511681A/ja not_active Ceased
- 2001-10-17 DE DE60132225T patent/DE60132225T2/de not_active Expired - Lifetime
- 2001-10-17 WO PCT/FR2001/003210 patent/WO2002033034A1/fr not_active Ceased
- 2001-10-17 BR BR0114624-6A patent/BR0114624A/pt not_active IP Right Cessation
- 2001-10-17 CA CA2426695A patent/CA2426695C/fr not_active Expired - Fee Related
- 2001-10-17 US US10/399,652 patent/US20040107505A1/en not_active Abandoned
- 2001-10-17 AT AT01978549T patent/ATE382672T1/de not_active IP Right Cessation
-
2007
- 2007-04-13 US US11/787,089 patent/US20070191254A1/en not_active Abandoned
-
2008
- 2008-07-02 US US12/166,941 patent/US20080263788A1/en not_active Abandoned
-
2010
- 2010-10-12 US US12/902,834 patent/US8128712B2/en not_active Expired - Fee Related
Non-Patent Citations (1)
| Title |
|---|
| See references of WO0233034A1 * |
Also Published As
| Publication number | Publication date |
|---|---|
| US20110028376A1 (en) | 2011-02-03 |
| FR2815355B1 (fr) | 2003-03-14 |
| FR2815355A1 (fr) | 2002-04-19 |
| US20080263788A1 (en) | 2008-10-30 |
| JP2004511681A (ja) | 2004-04-15 |
| ATE382672T1 (de) | 2008-01-15 |
| CA2426695C (fr) | 2011-11-29 |
| US20040107505A1 (en) | 2004-06-10 |
| DE60132225D1 (de) | 2008-02-14 |
| EP1326952B1 (fr) | 2008-01-02 |
| BR0114624A (pt) | 2003-12-23 |
| US8128712B2 (en) | 2012-03-06 |
| WO2002033034A1 (fr) | 2002-04-25 |
| DE60132225T2 (de) | 2008-12-18 |
| CA2426695A1 (fr) | 2002-04-25 |
| AU2002210655A1 (en) | 2002-04-29 |
| US20070191254A1 (en) | 2007-08-16 |
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