GB2303858A - Detergent composition - Google Patents
Detergent composition Download PDFInfo
- Publication number
- GB2303858A GB2303858A GB9515851A GB9515851A GB2303858A GB 2303858 A GB2303858 A GB 2303858A GB 9515851 A GB9515851 A GB 9515851A GB 9515851 A GB9515851 A GB 9515851A GB 2303858 A GB2303858 A GB 2303858A
- Authority
- GB
- United Kingdom
- Prior art keywords
- detergent composition
- composition according
- zeolite
- alkyl
- independently
- 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.)
- Withdrawn
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- 239000000203 mixture Substances 0.000 title claims abstract description 76
- 239000003599 detergent Substances 0.000 title claims abstract description 47
- -1 cationic ester Chemical class 0.000 claims abstract description 61
- 239000004094 surface-active agent Substances 0.000 claims abstract description 43
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 claims abstract description 42
- 239000010457 zeolite Substances 0.000 claims abstract description 42
- 229910021536 Zeolite Inorganic materials 0.000 claims abstract description 40
- 238000000034 method Methods 0.000 claims abstract description 13
- 239000004411 aluminium Substances 0.000 claims abstract description 7
- 229910052782 aluminium Inorganic materials 0.000 claims abstract description 7
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims abstract description 7
- 229910052710 silicon Inorganic materials 0.000 claims abstract description 7
- 239000010703 silicon Substances 0.000 claims abstract description 7
- 238000005054 agglomeration Methods 0.000 claims abstract description 6
- 230000002776 aggregation Effects 0.000 claims abstract description 6
- 239000007787 solid Substances 0.000 claims abstract description 6
- 125000000217 alkyl group Chemical group 0.000 claims description 27
- 125000003342 alkenyl group Chemical group 0.000 claims description 7
- 125000004432 carbon atom Chemical group C* 0.000 claims description 7
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 claims description 6
- 125000002877 alkyl aryl group Chemical group 0.000 claims description 6
- 239000002245 particle Substances 0.000 claims description 5
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 4
- 229940055076 parasympathomimetics choline ester Drugs 0.000 claims description 4
- 150000003248 quinolines Chemical class 0.000 claims description 4
- 125000006367 bivalent amino carbonyl group Chemical group [H]N([*:1])C([*:2])=O 0.000 claims description 3
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 claims description 3
- 125000005020 hydroxyalkenyl group Chemical group 0.000 claims description 3
- 229910052760 oxygen Inorganic materials 0.000 claims description 3
- 150000001450 anions Chemical class 0.000 claims description 2
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims 1
- 239000004576 sand Substances 0.000 claims 1
- 239000003093 cationic surfactant Substances 0.000 abstract description 7
- 238000003860 storage Methods 0.000 abstract description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 13
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 10
- 239000000463 material Substances 0.000 description 10
- 150000001875 compounds Chemical class 0.000 description 9
- 239000007844 bleaching agent Substances 0.000 description 8
- 239000002736 nonionic surfactant Substances 0.000 description 7
- 102000004190 Enzymes Human genes 0.000 description 6
- 108090000790 Enzymes Proteins 0.000 description 6
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 6
- 239000000843 powder Substances 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 5
- 125000000129 anionic group Chemical group 0.000 description 5
- 229960001231 choline Drugs 0.000 description 5
- 239000002243 precursor Substances 0.000 description 5
- 239000000377 silicon dioxide Substances 0.000 description 5
- 239000002689 soil Substances 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- 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 5
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerol Natural products OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 4
- KKCBUQHMOMHUOY-UHFFFAOYSA-N Na2O Inorganic materials [O-2].[Na+].[Na+] KKCBUQHMOMHUOY-UHFFFAOYSA-N 0.000 description 4
- 229910000323 aluminium silicate Inorganic materials 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 235000014113 dietary fatty acids Nutrition 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000000194 fatty acid Substances 0.000 description 4
- 229930195729 fatty acid Natural products 0.000 description 4
- 150000002191 fatty alcohols Chemical class 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 229910052708 sodium Inorganic materials 0.000 description 4
- 239000011734 sodium Substances 0.000 description 4
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 4
- 238000001694 spray drying Methods 0.000 description 4
- 108010065511 Amylases Proteins 0.000 description 3
- 102000013142 Amylases Human genes 0.000 description 3
- 102000005701 Calcium-Binding Proteins Human genes 0.000 description 3
- 108010045403 Calcium-Binding Proteins Proteins 0.000 description 3
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 3
- 229910000503 Na-aluminosilicate Inorganic materials 0.000 description 3
- 239000004115 Sodium Silicate Substances 0.000 description 3
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 3
- 150000008051 alkyl sulfates Chemical class 0.000 description 3
- 125000002947 alkylene group Chemical group 0.000 description 3
- 239000003945 anionic surfactant Substances 0.000 description 3
- 125000002091 cationic group Chemical group 0.000 description 3
- 229910052681 coesite Inorganic materials 0.000 description 3
- 229910052906 cristobalite Inorganic materials 0.000 description 3
- VTIIJXUACCWYHX-UHFFFAOYSA-L disodium;carboxylatooxy carbonate Chemical compound [Na+].[Na+].[O-]C(=O)OOC([O-])=O VTIIJXUACCWYHX-UHFFFAOYSA-L 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 150000004665 fatty acids Chemical class 0.000 description 3
- 239000002304 perfume Substances 0.000 description 3
- 229920001296 polysiloxane Polymers 0.000 description 3
- 150000004760 silicates Chemical class 0.000 description 3
- 235000012239 silicon dioxide Nutrition 0.000 description 3
- 239000002002 slurry Substances 0.000 description 3
- 239000000429 sodium aluminium silicate Substances 0.000 description 3
- 235000012217 sodium aluminium silicate Nutrition 0.000 description 3
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 3
- 229940045872 sodium percarbonate Drugs 0.000 description 3
- 229910052911 sodium silicate Inorganic materials 0.000 description 3
- 229910052938 sodium sulfate Inorganic materials 0.000 description 3
- 235000011152 sodium sulphate Nutrition 0.000 description 3
- MWNQXXOSWHCCOZ-UHFFFAOYSA-L sodium;oxido carbonate Chemical compound [Na+].[O-]OC([O-])=O MWNQXXOSWHCCOZ-UHFFFAOYSA-L 0.000 description 3
- 229910052682 stishovite Inorganic materials 0.000 description 3
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 3
- 229910052905 tridymite Inorganic materials 0.000 description 3
- 239000004382 Amylase Substances 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical group 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 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- 108091005804 Peptidases Proteins 0.000 description 2
- KFSLWBXXFJQRDL-UHFFFAOYSA-N Peracetic acid Chemical compound CC(=O)OO KFSLWBXXFJQRDL-UHFFFAOYSA-N 0.000 description 2
- 239000003377 acid catalyst Substances 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- 230000032683 aging Effects 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 235000019418 amylase Nutrition 0.000 description 2
- 230000003625 amylolytic effect Effects 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 150000001860 citric acid derivatives Chemical class 0.000 description 2
- DUYCTCQXNHFCSJ-UHFFFAOYSA-N dtpmp Chemical compound OP(=O)(O)CN(CP(O)(O)=O)CCN(CP(O)(=O)O)CCN(CP(O)(O)=O)CP(O)(O)=O DUYCTCQXNHFCSJ-UHFFFAOYSA-N 0.000 description 2
- 230000032050 esterification Effects 0.000 description 2
- 238000005886 esterification reaction Methods 0.000 description 2
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 2
- JPZROSNLRWHSQQ-UHFFFAOYSA-N furan-2,5-dione;prop-2-enoic acid Chemical compound OC(=O)C=C.O=C1OC(=O)C=C1 JPZROSNLRWHSQQ-UHFFFAOYSA-N 0.000 description 2
- 238000010348 incorporation Methods 0.000 description 2
- 229910052816 inorganic phosphate Inorganic materials 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical compound COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 description 2
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 2
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 2
- 125000000864 peroxy group Chemical group O(O*)* 0.000 description 2
- 229920005646 polycarboxylate Polymers 0.000 description 2
- 150000003138 primary alcohols Chemical class 0.000 description 2
- 239000000376 reactant Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- IBDSNZLUHYKHQP-UHFFFAOYSA-N sodium;3-oxidodioxaborirane;tetrahydrate Chemical compound O.O.O.O.[Na+].[O-]B1OO1 IBDSNZLUHYKHQP-UHFFFAOYSA-N 0.000 description 2
- 239000013042 solid detergent Substances 0.000 description 2
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 2
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 2
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 1
- RZRNAYUHWVFMIP-KTKRTIGZSA-N 1-oleoylglycerol Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(O)CO RZRNAYUHWVFMIP-KTKRTIGZSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- KEZYHIPQRGTUDU-UHFFFAOYSA-N 2-[dithiocarboxy(methyl)amino]acetic acid Chemical compound SC(=S)N(C)CC(O)=O KEZYHIPQRGTUDU-UHFFFAOYSA-N 0.000 description 1
- XSVSPKKXQGNHMD-UHFFFAOYSA-N 5-bromo-3-methyl-1,2-thiazole Chemical compound CC=1C=C(Br)SN=1 XSVSPKKXQGNHMD-UHFFFAOYSA-N 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- 125000006538 C11 alkyl 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])* 0.000 description 1
- 125000006539 C12 alkyl 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 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical group CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- 239000004365 Protease Substances 0.000 description 1
- 102100037486 Reverse transcriptase/ribonuclease H Human genes 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- 239000004902 Softening Agent Substances 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- ANBBXQWFNXMHLD-UHFFFAOYSA-N aluminum;sodium;oxygen(2-) Chemical compound [O-2].[O-2].[Na+].[Al+3] ANBBXQWFNXMHLD-UHFFFAOYSA-N 0.000 description 1
- 230000001668 ameliorated effect Effects 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000004061 bleaching Methods 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical class OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- CHBMMJFGTLSHKC-UHFFFAOYSA-N carbonic acid;oxirane Chemical compound C1CO1.OC(O)=O CHBMMJFGTLSHKC-UHFFFAOYSA-N 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- NEHMKBQYUWJMIP-NJFSPNSNSA-N chloro(114C)methane Chemical compound [14CH3]Cl NEHMKBQYUWJMIP-NJFSPNSNSA-N 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 229960002887 deanol Drugs 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 238000000280 densification Methods 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
- 238000007580 dry-mixing Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 230000036571 hydration Effects 0.000 description 1
- 238000006703 hydration reaction Methods 0.000 description 1
- 229910052739 hydrogen Chemical group 0.000 description 1
- 239000001257 hydrogen Chemical group 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 150000004668 long chain fatty acids Chemical class 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 150000002689 maleic acids Chemical class 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 125000005395 methacrylic acid group Chemical group 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
- 150000004967 organic peroxy acids Chemical class 0.000 description 1
- 238000000643 oven drying Methods 0.000 description 1
- 150000004965 peroxy acids Chemical class 0.000 description 1
- XCRBXWCUXJNEFX-UHFFFAOYSA-N peroxybenzoic acid Chemical compound OOC(=O)C1=CC=CC=C1 XCRBXWCUXJNEFX-UHFFFAOYSA-N 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920001983 poloxamer Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 235000019353 potassium silicate Nutrition 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000003352 sequestering agent Substances 0.000 description 1
- 229910001388 sodium aluminate Inorganic materials 0.000 description 1
- 239000012418 sodium perborate tetrahydrate Substances 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 235000019832 sodium triphosphate Nutrition 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- 108010075550 termamyl Proteins 0.000 description 1
- 150000004685 tetrahydrates Chemical class 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000008096 xylene 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
- C11D3/02—Inorganic compounds ; Elemental compounds
- C11D3/12—Water-insoluble compounds
- C11D3/124—Silicon containing, e.g. silica, silex, quartz or glass beads
- C11D3/1246—Silicates, e.g. diatomaceous earth
- C11D3/128—Aluminium silicates, e.g. zeolites
-
- 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/38—Cationic compounds
- C11D1/62—Quaternary ammonium compounds
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)
- Inorganic Chemistry (AREA)
- Detergent Compositions (AREA)
Abstract
A solid form detergent composition is disclosed containing (a) a zeolite builder comprising zeolite P having a silicon to aluminium ratio of not greater than 1.33 (zeolite MAP); and (b) a cationic ester surfactant wherein the pH of a 1% solution of said composition measured at 20{C is greater than 9.25. Granular detergent compositions made by agglomeration processes are preferred and methods of making such compositions are disclosed. The use of the zeolite MAP reduces the tendency of the cationic surfactant to hydrolyse on storage.
Description
DETERGENT COMPOSITION
The present invention relates to a granular alkaline detergent composition comprising a cationic ester surfactant and a zeolite component as a sequestering agent for water hardness.
Conventionally, water soluble inorganic phosphates, such as sodium tripolyphosphate, have been used as builders for laundry detergents.
More recently, alkali metal aluminosilicate ion-exchangers, particularly crystalline water insoluble sodium aluminosilicate zeolites, have been proposed as replacements for the inorganic phosphates.
For example, EP 21 491 A (Procter & Gamble) discloses detergent compositions containing a builder system which includes zeolite A, X or P (B) or a mixture thereof. EP 384070A (Unilever) discloses specific zeolite P materials having an especially low silicon to aluminium ratio not greater than 1.33 (hereinafter referred to as zeolite
MAP) and describes their use as detergency builders.
Surfactant components have traditionally been employed in detergent products to facilitate the removal of greasy soils/stains. In particular, surfactant systems comprising cationic esters have been found to be of utility in greasy soil/stain removal.
For example, EP-B-21,491 discloses detergent compositions containing a nonionic/cationic surfactant mixture and a builder mixture comprising aluminosilicate and polycarboxylate builder. The cationic surfactant may be a cationic ester. Improved particulate and greasy/oily soil removal is described.
US-A-4,228,042 discloses biodegradable cationic surfactants, including cationic ester surfactants for use in detergent compositions to provide greasy/oily soil removal. The combination of these cationic surfactants with nonionic surfactants in compositions designed for particulate soil removal is also described. Anionic surfactants are disclosed as optional components of the compositions, but are present at low levels relative to the cationic surfactant component.
US-A-4,239,660 discloses laundry detergent compositions containing cationic ester surfactant and nonionic surfactant at defined weight ratios and an alkalinity source. The alkalinity source enables a wash solution having a pH of from 8 to 10 to be fonned within 3 minutes of dissolution of the composition in water at 100OF (37OC) at a solution concentration of 0.15%.
US-A-4,260,529 discloses laundry detergent compositions having a pH of no greater than 11 containing cationic ester surfactant and nonionic surfactant at defined weight ratios. Anionic surfactants are disclosed as optional components of the compositions, but are present at low levels relative to the cationic surfactant component.
The Applicants have found that a problem with the use of cationic ester surfactants in solid alkaline detergent products is the propensity for the surfactant to degrade on storage. In more detail, the cationic ester surfactant has a tendency to be hydrolysed, particularly when stored under conditions of high moisture and/or elevated temperatures.
The Applicants have surprisingly found that this storage degradation problem may be ameliorated by the co-incorporation of a zeolite MAP builder material into the composition together with the cationic ester surfactant. The use of crystalline layered silicate as a cobuilder has been found to further aid cationic ester storage stability. In a preferred aspect, the zeolite MAP builder and optionally any cobuilder are in close physical proximity, more preferably in intimate admixture within the composition.
Whilst the prior art, as represented for example by European Patent
Aplications, EP 384070 A, EP 448297 A, EP 522726 A, EP 533392 A, EP 544492 A, EP 552053 A, and EP 552054 A has envisaged the use of surfactants in combination with zeolite MAP in laundry detergent compositions, none of these prior art documents specifically disclose the coincorporation of cationic ester surfactant with a zeolite MAP component in a solid detergent composition. Furthermore, none of these prior art documents provides any teaching relating to the surfactant storage stability problem addressed by the current invention, nor of any solution thereto involving the co-incorporation of a zeolite MAP builder component.
According to the present invention there is provided a solid form detergent composition containing (a) a zeolite builder comprising zeolite P having a silicon to aluminium
ratio of not greater than 1.33 (zeolite MAP); and (b) a cationic ester surfactant wherein the pH of a 1% solution of said composition measured at 20OC is greater than 9.25.
In a preferred aspect, the cationic ester surfactant is selected from those having the formula:
wherein R1 is a Cs-C31 linear or branched alkyl, alkenyl or alkaryl chain or
M-. N+(R6R7R8)(CH2)s; X and Y, independently, are selected from the group consisting of COO, OCO, O, CO, OCOO, CONH, NHCO, OCONH and NHCOO wherein at least one of X or Y is a COO, OCO, OCOO,
OCONH or NHCOO group;R2, R3, R4, Rs, R7, and R8 are independently selected from the group consisting of alkyl, alkenyl, hydroxyalkyl, hydroxyalkenyl and alkaryl groups having from 1 to 4 carbon atoms; and Rs is independently H or a Cl-C3 alkyl group; wherein the values of m, n, s and t independently lie in the range of from 0 to 8, the value of b lies in the range from 0 to 20, and the values of a, u and v independently are either 0 or 1 with the proviso that at least one of u or v must be 1; and wherein M is a counter anion.
Detailed description of the invention
Zeolite MAP builder
The first essential component of the present invention is a zeolite MAP builder, optionally in conjunction with one or more supplementary builders.
The zeolite MAP is typically present at a level of from 1% to 80%, more preferably from 15% to 40% by weight of the compositions.
Zeolite MAP is described in EP 384070A (Unilever). It is defined as an alkali metal alumino-silicate of the zeolite P type having a silicon to aluminium ratio not greater than 1.33, preferably within the range from 0.9 to 1.33 and more preferably within the range of from 0.9 to 1.2.
Of particular interest is zeolite MAP having a silicon to aluminium ratio not greater than 1.15 and, more particularly, not greater than 1.07.
Zeolite P having a Si:Al ratio of 1.33 or less may be prepared by the following steps:
(i) mixing together a sodium aluminate having a mole ratio Na2O:A1203 within the range of from 1.4 to 2.0 and a
sodium silicate having a mole ratio SiO2:Na20 within
the range of from 0.8 to 3.4 with vigorous stirring at a
temperature within the range of from 25"C to boiling
point usually 95"C, to give a gel having the following
composition;A1203: (1.75-3.5) SiO2 : (2.3-7.5) Na2O :P (80-450)H20; (ii) ageing the gel composition for 0.5 to 10 hours,
preferably 2 to 5 hours, at a temperature within the range
of from 70"C to boiling point, usually to 950C, with
sufficient stirring to maintain any solids present in
suspension;
(iii) separating the crystalline sodium aluminosilicate thus
formed, washing to a pH within the range of from 10 to
12.5, and drying, preferably at a temperature not
exceeding 150 C, to a moisture content of not less than 5
wt.%.
Preferred drying methods are spray-drying and flash drying. It appears that oven drying at too high a temperature may adversely affect the calcium binding capacity of the product under certain circumstances.
Commercial sodium metasilicate pentahydrate dissolved in water and commercial sodium silicate solution (waterglass) are both suitable silica sources for the production of zeolite P in accordance with the invention The reactants may be added together in any order either rapidly or slowly. Rapid addition at ambient temperature, and slow addition at elevated temperature (90-95"C) both give the desired product.
Vigorous stirring of the gel during the addition of the reactants, and at least moderate stirring during the subsequent ageing step, however, appear to be essential for the formation of pure zeolite P. In the absence of stirring, various mixtures of crystalline and amorphous materials may be obtained.
Zeolite MAP generally has a calcium binding capacity of at least 150 mg CaO per g of anhydrous aluminosilcate, as measured by the standard method described in GB 1473201 (Henkel). The calcium binding capacity is normally 160 mg CaO/g and may be as high 170 mg
CaO/g.
Although zeolite MAP like other zeolites contains water of hydration, for the purposes of the present invention amounts and percentages of zeolite are expressed in terms of the notional anhydrous material.
The amount of water present in hydrated zeolite MAP at ambient temperature and humidity is generally about 20 wt.%.
In a preferred aspect the zeolite MAP detergent builder has a particle size, expressed as a d50 value of from 1.0 to 10.0 micrometres, more preferably from 2.0 to 7.0 micrometres, most preferably from 2.5 to 5.0 micrometres.
The d50 value indicates that 50% by weight of the particles have a diameter smaller than that figure. The particle size may, in particular be determined by conventional analytical techniques such as microscopic determination using a scanning electron microscope or by means of a laser granulometer. Other methods of establishing dso values are disclosed in EP 384070A.
Cationic ester surfactant
The second essential element of the detergent compositions of the invention is a cationic ester surfactant. That is, a preferably water dispersible compound having surfactant properties comprising at least one hydrolysable ester (ie -COO-) linkage and at least one cationically charged group.
The cationic ester surfactant is present in amount from 0.1% to 90%, preferably from 0.5% to 40%, most preferably from 1% to 10% by weight of the detergent composition.
The weight ratio of zeolite MAP to cationic ester component is typically from 100:1 to 2:1, preferably from 50:1 to 3:1, most preferably from 30:1 to
Suitable cationic ester surfactants, including choline ester surfactants, have for example been disclosed in US Patents No.s 4228042, 4239660 and 4260529.
Preferred water dispersible cationic ester surfactants are those having the formula:
wherein R1 is a Cs-C31 linear or branched alkyl, alkenyl or alkaryl chain or
M-. N+(R6R7Rg)(CH2)S; X and Y, independently, are selected from the group consisiting of COO, OCO, O, CO, OCOO, CONH, NHCO, OCONH and NHCOO wherein at least one of X or Y is a COO, OCO, OCOO,
OCONH or NHCOO group;R2, R3, R4, R6, R7, and R8 are independently selected from the group consisting of alkyl, alkenyl, hydroxyalkyl, hydroxyalkenyl and alkaryl groups having from 1 to 4 carbon atoms; and R5 is independently H or a Cl-C3 alkyl group; wherein the values of m, n, s and t independently lie in the range of from 0 to 8, the value of b lies in the range from 0 to 20, and the values of a, u and v independently are either 0 or 1 with the proviso that at least one of u or v must be 1; and wherein M is a counter union.
Preferably R2,R3 and R4 are independently selected from CH3 and -CH2CH20H.
Preferably M is selected from the group consisting of halide, methyl sulfate, sulfate, and nitrate, more preferably methyl sulfate, chloride, bromide or iodide.
Preferred water dispersible cationic ester surfactants are the choline esters having the formula:
wherein R1 is a Cl 1-C19 linear or branched alkyl chain.
Particularly preferred choline esters of this type include the stearoyl choline ester quaternary methylammonium halides (R1=C17 alkyl), palmitoyl choline ester quaternary methylammonium halides (Rl=C15 alkyl), myristoyl choline ester quaternary methylammonium halides (R1=C13 alkyl), lauroyl choline ester methylammonium halides (Rl=C11 alkyl), cocoyl choline ester quaternary methylammonium halides (Rl=Cl l C13 alkyl), tallowyl choline ester quaternary methylammonium halides (R1=Ci 5- C17 alkyl), and any mixtures thereof.
Most preferred choline ester compounds among the above disclosed are cocoyl choline ester quaternary methylammonium halides.
The particularly preferred choline esters, given above, may be prepared by the direct esterification of a fatty acid or fatty acid mixture of the desired chain length with dimethylaminoethanol, in the presence of an acid catalyst.
The reaction product is then quaternized in a suitable solvent (e.g. water, ethanol, fatty acid) with a methyl halide, forming the desired cationic material.
They may also be prepared by the direct esterification of a long chain fatty acid of the desired chain length together with 2-haloethanol, in the presence of an acid catalyst material. The reaction product is then quaternized with trimethylamine, forming the desired cationic material.
Other suitable cationic ester surfactants have the structural formulas below, wherein d may be from 0 to 20.
DH of the compositions
The present compositions have a pH measured as a 1% solution in distilled water of at least 9.25, preferably from 10.0 to 12.5, most preferably from 10.5 to 12.0.
Additional detergent components
The detergent composition according to the invention may contain other detergent components such as surfactants, cobuilders, bleaches, fluorescers, antiredeposition agents, inorganic salts such as sodium sulphate, enzymes, lather control agents, fabric softening agents, pigments, coloured speckles and perfumes.
Surfactant
The detergent composition according to the invention preferably includes an additional surfactant selected from anionics, nonionics, zwitterionics, ampholytics and non-cationic ester cationics.
The additional surfactant is preferably present in the detergent compositions at a level of from 1% to 50%, preferably from 3% to 30%, most preferably from 5% to 20% by weight of the compositions.
Many suitable detergent-active compounds are available and fully described in the literature (for example "Surface Active Agents and
Detergents" Volumes I and II by Schwartz, Perry and Berch).
Examples of suitable additional anionic surfactants include anionic sulfates, olefin sulphonates, alkyl xylene sulphonates, dialkylsulphosuccinates, and fatty acid ester sulphonates. Sodium salts are generally preferred.
Anionic sulfate surfactant
Anionic sulfate surfactants suitable for use herein include the linear and branched primary alkyl sulfates, alkyl ethoxysulfates, fatty oleoyl glycerol sulfates, alkyl phenol ethylene oxide ether sulfates, the Cs-C17 acyl-N-(C 1- C4 alkyl) and -N-(C1-C2 hydroxyalkyl) glucamine sulfates, and sulfates of alkylpolysaccharides such as the sulfates of alkylpolyglucoside (the nonionic nonsulfated compounds being described herein).
Alkyl ethoxysulfate surfactants are preferably selected from the group consisting of the C6-C18 alkyl sulfates which have been ethoxylated with from 0.5 to 20 moles of ethylene oxide per molecule. More preferably, the alkyl ethoxysulfate surfactant is a C6-C18 alkyl sulfate which has been ethoxylated with from 0.5 to 20, preferably from 0.5 to 5, moles of ethylene oxide per molecule.
Anionic sulfonate surfactant
Anionic sulfonate surfactants suitable for use herein include the salts of Cs- C20 linear alkylbenzene sulfonates, alkyl ester sulfonates, C6-C22 primary or secondary alkane sulfonates, C6-C24 olefin sulfonates, sulfonated polycarboxylic acids, alkyl glycerol sulfonates, fatty acyl glycerol sulfonates, fatty oleyl glycerol sulfonates, and any mixtures thereof.
Nonionic surfactant
Examples of suitable alkoxylated nonionic surfactants include alkoxylated adducts of fatty alcohols containing an average of from 1 to 7 alkylene oxide groups per molecule.
The alkylene oxide residues may, for example, be ethylene oxide residues or mixtures thereof with propylene oxide residues.
Preferred alkylene oxide adducts of fatty alcohols useful in the present invention can suitably be chosen from those of the general formula:
R-O-(CnH2nO)yH wherein R is an alkyl or alkenyl group having at least 10 carbon atoms, most preferably from 10 to 22 carbon atoms, y is from 0.5 to S and n is 2 or 3.
Suitable nonionic surfactants include primary C11-C15 aliphatic alcohols condensed with an average of no more than five ethylene oxide groups per mole of alcohol, having an ethylene oxide content of less than 50% by weight, preferably from 25% to less than 50% by weight.
A preferred aliphatic alcohol ethoxylated is a primary alcohol having an average of 12 to 15 carbon atoms in the alkyl chain condensed with an average of three ethoxy groups per mole of alcohol.
Specific examples of suitable alkoxylated adducts of fatty alcohols are
Synperonic A3 (ex ICI), which is a C 13-Cl 5 alcohol with about three ethylene oxide groups per molecule and Empilan KB3 (ex Marchon), which is lauric alcohol 3EO.
Another class of nonionic sufactants comprises alkyl polyglucoside compounds of general formula
RO(CnH2nO)tZx wherein Z is a moiety derived from glucose; R is a saturated hydrophobic alkyl group that contains from 12 to 18 carbon atoms; t is from 0 to 10 and n is 2 or 3; xis from 1.1 to 4, the compounds including less than 10% unreacted fatty alcohol and less than 50% short chain alkyl polyglucosides. Compounds of this type and their use in detergent compositions are disclosed in EP-B 0070074, 0070077, 0075996 and 0094118.
Cobuilders
In addition to zeolite MAP, the builder system may contain an organic or inorganic cobuilder.
Suitable organic cobuilders can be monomeric or polymeric carboxylates such as citrates or polymers of acrylic, methacrylic and/or maleic acids in neutralised form. Suitable inorganic cobuilders include carbonates and amorphous and crystalline layered silicates. Crystalline layered silicates are most preferred.
Suitable crystalline layered silicates have the composition: NaMSix02x+l yH20 where M is sodium or hydrogen, preferably sodium; x is a number from 1.9 to 4; and y is a number from 0 to 20. Such materials are described in US Patents No. 4664839; No. 4728443 and No. 4820439 (Hoechst
AG). Especially preferred are compounds in which x = 2 and y = 0.
The synthetic material is commercially available from Hoechst AG as 6 -Na2 Si2O5 (SKS6) and is described in US Patent No. 4664830.
The cobuilder may include an aluminosilicate zeolite A material, but where present such zeolite A builder is at a level of no more than 2% by weight of the detergent composition. Preferably the detergent composition is free of zeolite A.
The total amount of detergency builder in the granular composition typically ranges from 1 to 80 wt.%, more preferably from 15 to 60 wt% and most preferably from 10 to 45 wt.%.
Bleach
Detergent compositions according to the invention may also suitably contain a bleach system. This preferably comprises one or more peroxy bleach compounds, for example, inorganic persalts or organic peroxyacids, which may be employed in conjunction with bleach precursors to improve bleaching action at low temperatures.
The bleach system preferably comprises a peroxy bleach compound, preferably an inorganic persalt, optionally in conjunction with a peroxyacid bleach precursor. Suitable persalts include sodium perborate monohydrate and tetrahydrate and sodium percarbonate, with sodium percarbonate being most preferred. In one preferred aspect the composition is substantially free of perborate tetrahydrate to ensure good storage stability of the composition at elevated temperatures.
Preferred bleach precursors are peracetic acid precursors, such as tetraacetylethylene diamine (TAED); peroxybenzoic acid precursors.
Phvsical form
The detergent composition according to the invention is in solid form, for example powder, granular or tablet form. However, granular compositions are preferred.
In a preferred aspect at least part of, more preferably all of the cationic ester surfactant is in close physical proximity to the zeolite MAP component in the composition, preferably the two components are in close contact, most preferably they are in intimate admixture. Particles, particularly made by agglomeration methods, in which such close physical proximity and especially such intimate admixture may be achieved are especially preferred. Suitable coagglomerate materials include polycarboxylate builders, especially citrates, crystalline layered silicate, carbonate and bicarbonate salts.
Making process
The solid detergent compositions of the invention may be prepared by any suitable method. Particulate detergent compositions are suitably prepared by any tower (spray-drying) or non-tower process.
In processes based around a spray-drying tower, a base powder is first prepared by spray-drying a slurry and then other components unsuitable for processing via the slurry can be sprayed on or admixed (postdosed).
The zeolite MAP is suitable for inclusion in the slurry, although it may be advantageous for processing reasons for part of the zeolite MAP to be incorporated post-tower.
In a preferred aspect, particulate detergent compositions in accordance with the invention may be prepared by wholly non-tower processes such as agglomeration using any commonly known detergent agglomeration methods.
Granular detergent compositions of the invention may be prepared to any suitable bulk density. The compositions preferably have a bulk density of at least 400 g/l preferably at least 550 g/l, most preferably at least 700 g/l and, with particular preference at least 800 g/l.
The benefits of the present invention are particularly evident in powders of high bulk density, for example, of 700 g/l or above. Such powders may be prepared either by post-tower densification of spraydried powder, or by wholly non-tower methods such as dry mixing and agglomeration; in both cases a high-speed mixer/granulator may advantageously be used. Processes using high-speed mixer/granulators are disclosed, for example, in EP340 013A, EP 367 339A, EP 390 251A and EP 420 317A (Unilever).
Illustrative compositions according to the present invention are presented in the following Examples.
In the detergent compositions, the abbreviated component identifications have the following meanings:
Cationic ester RlCOOCH2CH2.N+(CH3)3Cl- with R1 = C11- C13
246AS Sodium alkyl sulfate surfactant containing a
alkyl chain length weight distribution of 15% C12
alkyl chains, 45% C14 alkyl chains, 35% C16
alkyl chains, 5% C18 alkyl chains
LAS C12 linear alkylbenzene sulfonate
TAS Sodium alkyl sulfate surfactant containing
predominantly C16 - C18 alkyl chains derived
from tallow oil.
24AE3S C12-C14 alkyl ethoxysulfate containing an
average of three ethoxy groups per mole
XYEZ A C1X-IY primary alcohol condensed with an
average of Z moles of ethylene oxide
Carbonate Anhydrous sodium carbonate
Perborate Sodium perborate tetrahydrate
Percarbonate Sodium percarbonate
TAED Tetra acetyl ethylene diamine
Silicate Amorphous Sodium Silicate (SiO2:Na20 ratio
normally follows)
Zeolite MAP Hydrated sodium aluminosilicate zeolite MAP
having a silicon to aluminium ratio of 1.07
MA/AA Copolymer of 1:4 maleic/acrylic acid, average
molecular weight about 80,000.
Amylase Amylolytic enzyme sold under the tradename
Termamyl 60T by Novo Industries A/S (approx
0.9% enzyme activity)
BSA Amylolytic enzyme sold under the tradename
LE17 by Novo Industries A/S (approx 1%
enzyme activity)
Protease Proteolytic enzyme sold by Novo Industries AS
of activity 4.0 KNPU
DTPMP Diethylene triamine penta (methylene phosphonic
acid)
Silicone suds suppressor 12% silicone/silica, 18% stearyl alcohol, 70% starch in granular form.
Example 1
The following granular laundry detergent compositions were prepared (parts by weight) in accordance with the invention. All amylase enzyme levels relate to levels of active enzyme, expressed on a 4 KNU/g activity basis.
A B C D E Cationic ester 2.0 1.5 1.0 0.5 3.0 246AS 7.6 6.5 4.8 6.8 TAS - - - 8.6 24AE3S 2.4 - 1.2 1.7 - 25E3 3.26 - - - 6.3 35E3 5.0 5.0 5.0 Zeolite MAP 20.0 25.0 20.0 25.0 31.0 Carbonate 15.0 15.0 20.0 10.0 12.0 MA/AA 4.25 4.25 4.25 4.25 2.0 Perborate - 16.0 - 16.0 20.0 Percarbonate 20.0 - 20.0 - TAED 5.0 5.0 5.0 5.0 6.7 Amylase 0.2 0.5 - 0.1 0.1 BSA 0.2 Protease 0.04 0.08 - 0.05 0.05 Silicate (2.0 4.0 - - 4.0 3.0 ratio Water and miscellaneous (Including suds suppressor, sodium sulphate, perfUme) to balance
Example 2
The following high density granular detergent formulations, according to the present invention were prepared::
F G H Blown Powder Zeolite MAP 13.0 10.0 25.0 MA/AA 4.0 3.6 5.0 DI?MP 0.4 0.4 0.5 Magnesium sulfate 0.4 0.4 0.4 Surfactant agglomerate LAS 7.0 6.8 9.0 TAS 2.0 1.4 2.6 Zeolite MAP 7.0 6.6 9.0 Carbonate 7.0 6.8 9.0 Cationic ester agglomerate LAS 1.8 1.8 3.6 Cationic ester 1.0 1.0 2.0 Bentonite clay 12.0 Sodium sulfate 3.0 - 6.0 Silicate (2.8 ratio) - 1.0 Zeolite MAP 4.0 2.0 8.0 Spray On Perfume 0.3 0.3 0.3 Silicone suds suppressor 0.5 0.5 0.5 45E7 4.0 2.0 4.0 68E11 1.0 1.0 1.0 Dry additives Percarbonate 20.0 20.0 TAED 5.0 5.0 Balance (Moisture and 100.0 100.0 100.0 Miscellaneous) Density itre 850 850 850
Claims (11)
- CLAIMS 1. A solid form detergent composition containing (a) a zeolite builder comprising zeolite P having a silicon to aluminium ratio of not greater than 1.33 (zeolite MAP); and (b) a cationic ester surfactant wherein the pH of a 1% solution of said composition measured at 200C is greater than 9.25.
- 2. A detergent composition according to Claim 1 wherein said zeolite builder is present at a level of from 1% to 80% by weight of the composition
- 3. A detergent composition according to either Claims 1 or 2 wherein said zeolite MAP builder has a particle size, expressed as a d5o value of from 1.0 to 10.0 micrometres.
- 4. A detergent composition according to any of Claims 1 to 3 wherein said cationic ester surfactant is selected from those having the formula:wherein R1 is a C5-C31 linear or branched alkyl, alkenyl or alkaryl chain or M-. N+(R6R7R8)(CH2)s; X and Y, independently, are selected from the group consisting of COO, OCO, O, CO, OCOO, CONH, NHCO, OCONH and NHCOO wherein at least one of X or Y is a COO, OCO, OCOO, OCONH or NHCOO group;R2, R3, R4, R6, R7, and R8 are independently selected from the group consisting of alkyl, alkenyl, hydroxyalkyl, hydroxy-alkenyl and alkaryl groups having from 1 to 4 carbon atoms; and R5 is independently H or a C 1- C3 alkyl group; wherein the values ofm, n, sand t independently lie in the range of from 0 to 8, the value of b lies in the range from 0 to 20, and the values of a, u and v independently are either 0 or 1 with the proviso that at least one of u or v must be 1; and wherein M is a counter anion.
- 5. A detergent composition according to Claim 4 wherein R2,R3 and R4 are independently selected from the group consisting of CH3 and CH2CH20H.
- 6. A detergent composition according to Claim 4 wherein the cationic ester is selected from the choline esters having the formula:wherein R1 is a Cl l-Clg linear or branched alkyl chain.
- 7. A detergent composition according to any of Claims 1 to 6 containing an additional surfactant at a level of from 1% to 50% by weight of the composition.
- 8. A detergent composition according to any of Claims 1 to 7 containing an organic or inorganic cobuilder.
- 9. A detergent composition according to Claim 8 wherein said cobuilder is a crystalline layered silicate builder.
- 10. A detergent composition according to any of Claims 1 to 9 wherein said composition is in particulate form.
- 11. A particulate detergent composition according to Claim 10 made by an agglomeration process.
Priority Applications (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB9515851A GB2303858A (en) | 1995-08-02 | 1995-08-02 | Detergent composition |
| PCT/US1996/012503 WO1997005221A1 (en) | 1995-08-02 | 1996-07-31 | Detergent composition |
| ARP960103856A AR003172A1 (en) | 1995-08-02 | 1996-08-02 | ALKALINE DETERGENT COMPOSITION IN THE FORM OF GRANULES. |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB9515851A GB2303858A (en) | 1995-08-02 | 1995-08-02 | Detergent composition |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| GB9515851D0 GB9515851D0 (en) | 1995-10-04 |
| GB2303858A true GB2303858A (en) | 1997-03-05 |
Family
ID=10778656
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB9515851A Withdrawn GB2303858A (en) | 1995-08-02 | 1995-08-02 | Detergent composition |
Country Status (3)
| Country | Link |
|---|---|
| AR (1) | AR003172A1 (en) |
| GB (1) | GB2303858A (en) |
| WO (1) | WO1997005221A1 (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19721885A1 (en) † | 1997-05-26 | 1998-12-03 | Henkel Kgaa | Process for the production of granules containing cationic surfactants |
| DE19948671A1 (en) * | 1999-10-08 | 2001-04-19 | Cognis Deutschland Gmbh | laundry detergent |
| US20070130694A1 (en) * | 2005-12-12 | 2007-06-14 | Michaels Emily W | Textile surface modification composition |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4239660A (en) * | 1978-12-13 | 1980-12-16 | The Procter & Gamble Company | Detergent composition comprising a hydrolyzable cationic surfactant and specific alkalinity source |
| EP0533392A2 (en) * | 1991-09-18 | 1993-03-24 | Unilever Plc | Detergent compositions |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4260529A (en) * | 1978-06-26 | 1981-04-07 | The Procter & Gamble Company | Detergent composition consisting essentially of biodegradable nonionic surfactant and cationic surfactant containing ester or amide |
| NL7815014A (en) * | 1977-06-29 | 1979-10-31 | Procter & Gamble | LIQUID DETERGENT FOR BETTER REMOVAL OF GREASE DIRT. |
| ATE5896T1 (en) * | 1979-11-03 | 1984-02-15 | The Procter & Gamble Company | GRANULAR DETERGENT COMPOSITIONS. |
| GB9113674D0 (en) * | 1991-06-25 | 1991-08-14 | Unilever Plc | Detergent compositions |
| GB9305599D0 (en) * | 1993-03-18 | 1993-05-05 | Unilever Plc | Detergent compositions |
-
1995
- 1995-08-02 GB GB9515851A patent/GB2303858A/en not_active Withdrawn
-
1996
- 1996-07-31 WO PCT/US1996/012503 patent/WO1997005221A1/en not_active Ceased
- 1996-08-02 AR ARP960103856A patent/AR003172A1/en unknown
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4239660A (en) * | 1978-12-13 | 1980-12-16 | The Procter & Gamble Company | Detergent composition comprising a hydrolyzable cationic surfactant and specific alkalinity source |
| EP0533392A2 (en) * | 1991-09-18 | 1993-03-24 | Unilever Plc | Detergent compositions |
Also Published As
| Publication number | Publication date |
|---|---|
| AR003172A1 (en) | 1998-07-08 |
| GB9515851D0 (en) | 1995-10-04 |
| WO1997005221A1 (en) | 1997-02-13 |
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