US3485761A - Production of detergent compositions containing finely dispersed optical brighteners - Google Patents
Production of detergent compositions containing finely dispersed optical brighteners Download PDFInfo
- Publication number
- US3485761A US3485761A US616195A US3485761DA US3485761A US 3485761 A US3485761 A US 3485761A US 616195 A US616195 A US 616195A US 3485761D A US3485761D A US 3485761DA US 3485761 A US3485761 A US 3485761A
- Authority
- US
- United States
- Prior art keywords
- detergent
- brightener
- sodium
- composition
- acid
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000000203 mixture Substances 0.000 title description 88
- 239000003599 detergent Substances 0.000 title description 81
- 230000003287 optical effect Effects 0.000 title description 13
- 239000002904 solvent Substances 0.000 description 33
- 235000014113 dietary fatty acids Nutrition 0.000 description 22
- 239000000194 fatty acid Substances 0.000 description 22
- 229930195729 fatty acid Natural products 0.000 description 22
- 150000004665 fatty acids Chemical class 0.000 description 21
- -1 5-methyl benzoxazolyl Chemical group 0.000 description 19
- 239000011734 sodium Substances 0.000 description 19
- 229910052708 sodium Inorganic materials 0.000 description 19
- 150000001408 amides Chemical class 0.000 description 18
- 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 description 17
- 239000008187 granular material Substances 0.000 description 15
- 125000004432 carbon atom Chemical group C* 0.000 description 13
- 239000004094 surface-active agent Substances 0.000 description 12
- 150000003839 salts Chemical class 0.000 description 11
- 239000004615 ingredient Substances 0.000 description 10
- 238000000034 method Methods 0.000 description 10
- 239000011591 potassium Substances 0.000 description 10
- 229910052700 potassium Inorganic materials 0.000 description 10
- 239000002002 slurry Substances 0.000 description 10
- 239000003240 coconut oil Substances 0.000 description 8
- 235000019864 coconut oil Nutrition 0.000 description 8
- 239000003760 tallow Substances 0.000 description 8
- 239000004753 textile Substances 0.000 description 8
- 125000002252 acyl group Chemical group 0.000 description 7
- 125000000217 alkyl group Chemical group 0.000 description 7
- 239000007921 spray Substances 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 239000007788 liquid Substances 0.000 description 6
- 239000000271 synthetic detergent Substances 0.000 description 6
- 125000000129 anionic group Chemical group 0.000 description 5
- 235000019832 sodium triphosphate Nutrition 0.000 description 5
- 235000013162 Cocos nucifera Nutrition 0.000 description 4
- 244000060011 Cocos nucifera Species 0.000 description 4
- 229920004934 Dacron® Polymers 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 239000005977 Ethylene Substances 0.000 description 4
- 239000004677 Nylon Substances 0.000 description 4
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 4
- 150000001298 alcohols Chemical class 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 229920001778 nylon Polymers 0.000 description 4
- IPCSVZSSVZVIGE-UHFFFAOYSA-N palmitic acid group Chemical group C(CCCCCCCCCCCCCCC)(=O)O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 4
- 239000005020 polyethylene terephthalate Substances 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 238000005507 spraying Methods 0.000 description 4
- 229920002994 synthetic fiber Polymers 0.000 description 4
- 239000004758 synthetic textile Substances 0.000 description 4
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 3
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 229910052783 alkali metal Inorganic materials 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Natural products N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 3
- 229940077388 benzenesulfonate Drugs 0.000 description 3
- 238000005282 brightening Methods 0.000 description 3
- 239000007795 chemical reaction product Substances 0.000 description 3
- 230000008021 deposition Effects 0.000 description 3
- UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 239000000344 soap Substances 0.000 description 3
- 229910052938 sodium sulfate Inorganic materials 0.000 description 3
- 235000011152 sodium sulphate Nutrition 0.000 description 3
- SOBHUZYZLFQYFK-UHFFFAOYSA-K trisodium;hydroxy-[[phosphonatomethyl(phosphonomethyl)amino]methyl]phosphinate Chemical compound [Na+].[Na+].[Na+].OP(O)(=O)CN(CP(O)([O-])=O)CP([O-])([O-])=O SOBHUZYZLFQYFK-UHFFFAOYSA-K 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 239000004115 Sodium Silicate Substances 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
- 150000004996 alkyl benzenes Chemical class 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 230000002708 enhancing effect Effects 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- VKOBVWXKNCXXDE-UHFFFAOYSA-N icosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCC(O)=O VKOBVWXKNCXXDE-UHFFFAOYSA-N 0.000 description 2
- 238000010348 incorporation Methods 0.000 description 2
- SUMDYPCJJOFFON-UHFFFAOYSA-N isethionic acid Chemical compound OCCS(O)(=O)=O SUMDYPCJJOFFON-UHFFFAOYSA-N 0.000 description 2
- 238000004900 laundering Methods 0.000 description 2
- MBKDYNNUVRNNRF-UHFFFAOYSA-N medronic acid Chemical compound OP(O)(=O)CP(O)(O)=O MBKDYNNUVRNNRF-UHFFFAOYSA-N 0.000 description 2
- HNEGQIOMVPPMNR-NSCUHMNNSA-N mesaconic acid Chemical compound OC(=O)C(/C)=C/C(O)=O HNEGQIOMVPPMNR-NSCUHMNNSA-N 0.000 description 2
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 2
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 2
- 235000021317 phosphate Nutrition 0.000 description 2
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 2
- 229920005646 polycarboxylate Polymers 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 159000000001 potassium salts Chemical class 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 2
- 229910052911 sodium silicate Inorganic materials 0.000 description 2
- 238000001694 spray drying Methods 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- 239000001124 (E)-prop-1-ene-1,2,3-tricarboxylic acid Substances 0.000 description 1
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
- PSZAEHPBBUYICS-UHFFFAOYSA-N 2-methylidenepropanedioic acid Chemical compound OC(=O)C(=C)C(O)=O PSZAEHPBBUYICS-UHFFFAOYSA-N 0.000 description 1
- KDSNLYIMUZNERS-UHFFFAOYSA-N 2-methylpropanamine Chemical class CC(C)CN KDSNLYIMUZNERS-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- 235000021357 Behenic acid Nutrition 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- IMQLKJBTEOYOSI-GPIVLXJGSA-N Inositol-hexakisphosphate Chemical compound OP(O)(=O)O[C@H]1[C@H](OP(O)(O)=O)[C@@H](OP(O)(O)=O)[C@H](OP(O)(O)=O)[C@H](OP(O)(O)=O)[C@@H]1OP(O)(O)=O IMQLKJBTEOYOSI-GPIVLXJGSA-N 0.000 description 1
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical class NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 1
- SUZRRICLUFMAQD-UHFFFAOYSA-N N-Methyltaurine Chemical compound CNCCS(O)(=O)=O SUZRRICLUFMAQD-UHFFFAOYSA-N 0.000 description 1
- HWZUDASOMGNLSM-UHFFFAOYSA-N O=P1OCOP(=O)O1 Chemical class O=P1OCOP(=O)O1 HWZUDASOMGNLSM-UHFFFAOYSA-N 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- KREOUCZKLVCRAQ-UHFFFAOYSA-N P1(=O)OCOP(O1)=O.[K].[K].[K] Chemical compound P1(=O)OCOP(O1)=O.[K].[K].[K] KREOUCZKLVCRAQ-UHFFFAOYSA-N 0.000 description 1
- 235000019482 Palm oil Nutrition 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- IMQLKJBTEOYOSI-UHFFFAOYSA-N Phytic acid Natural products OP(O)(=O)OC1C(OP(O)(O)=O)C(OP(O)(O)=O)C(OP(O)(O)=O)C(OP(O)(O)=O)C1OP(O)(O)=O IMQLKJBTEOYOSI-UHFFFAOYSA-N 0.000 description 1
- 229920000388 Polyphosphate Polymers 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 229940091181 aconitic acid Drugs 0.000 description 1
- 229910000288 alkali metal carbonate Inorganic materials 0.000 description 1
- 150000008041 alkali metal carbonates Chemical class 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 238000010936 aqueous wash Methods 0.000 description 1
- 229940116226 behenic acid Drugs 0.000 description 1
- SRSXLGNVWSONIS-UHFFFAOYSA-M benzenesulfonate Chemical compound [O-]S(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-M 0.000 description 1
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 1
- 239000012964 benzotriazole Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- GTZCVFVGUGFEME-IWQZZHSRSA-N cis-aconitic acid Chemical compound OC(=O)C\C(C(O)=O)=C\C(O)=O GTZCVFVGUGFEME-IWQZZHSRSA-N 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 235000011180 diphosphates Nutrition 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 150000002193 fatty amides Chemical class 0.000 description 1
- 229940013317 fish oils Drugs 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 125000005456 glyceride group Chemical group 0.000 description 1
- PEDCQBHIVMGVHV-UHFFFAOYSA-N glycerol Substances OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 1
- 239000008233 hard water Substances 0.000 description 1
- 230000036571 hydration Effects 0.000 description 1
- 238000006703 hydration reaction Methods 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 1
- 229940045996 isethionic acid Drugs 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 235000020778 linoleic acid Nutrition 0.000 description 1
- OYHQOLUKZRVURQ-HZJYTTRNSA-N linoleic acid group Chemical group C(CCCCCCC\C=C/C\C=C/CCCCC)(=O)O OYHQOLUKZRVURQ-HZJYTTRNSA-N 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
- 239000011976 maleic acid Substances 0.000 description 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N methanol Substances OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- HNEGQIOMVPPMNR-UHFFFAOYSA-N methylfumaric acid Natural products OC(=O)C(C)=CC(O)=O HNEGQIOMVPPMNR-UHFFFAOYSA-N 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- FATBGEAMYMYZAF-KTKRTIGZSA-N oleamide Chemical compound CCCCCCCC\C=C/CCCCCCCC(N)=O FATBGEAMYMYZAF-KTKRTIGZSA-N 0.000 description 1
- FATBGEAMYMYZAF-UHFFFAOYSA-N oleicacidamide-heptaglycolether Natural products CCCCCCCCC=CCCCCCCCC(N)=O FATBGEAMYMYZAF-UHFFFAOYSA-N 0.000 description 1
- VSXGXPNADZQTGQ-UHFFFAOYSA-N oxirane;phenol Chemical compound C1CO1.OC1=CC=CC=C1 VSXGXPNADZQTGQ-UHFFFAOYSA-N 0.000 description 1
- 239000002540 palm oil Substances 0.000 description 1
- 229940068041 phytic acid Drugs 0.000 description 1
- 235000002949 phytic acid Nutrition 0.000 description 1
- 239000000467 phytic acid Substances 0.000 description 1
- 239000001205 polyphosphate Substances 0.000 description 1
- 235000011176 polyphosphates Nutrition 0.000 description 1
- 235000013966 potassium salts of fatty acid Nutrition 0.000 description 1
- 235000019353 potassium silicate Nutrition 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 239000003352 sequestering agent Substances 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 235000013875 sodium salts of fatty acid Nutrition 0.000 description 1
- 235000019351 sodium silicates Nutrition 0.000 description 1
- KVCGISUBCHHTDD-UHFFFAOYSA-M sodium;4-methylbenzenesulfonate Chemical compound [Na+].CC1=CC=C(S([O-])(=O)=O)C=C1 KVCGISUBCHHTDD-UHFFFAOYSA-M 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000013042 solid detergent Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 230000001180 sulfating effect Effects 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 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
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M23/00—Treatment of fibres, threads, yarns, fabrics or fibrous goods made from such materials, characterised by the process
-
- 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
- C11D10/00—Compositions of detergents, not provided for by one single preceding group
- C11D10/04—Compositions of detergents, not provided for by one single preceding group based on mixtures of surface-active non-soap compounds and soap
-
- 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
- C11D11/00—Special methods for preparing compositions containing mixtures of detergents
- C11D11/02—Preparation in the form of powder by spray drying
-
- 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
- C11D3/04—Water-soluble compounds
- C11D3/06—Phosphates, including polyphosphates
-
- 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
- C11D3/40—Dyes ; Pigments
- C11D3/42—Brightening agents ; Blueing agents
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M11/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
- D06M11/68—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with phosphorus or compounds thereof, e.g. with chlorophosphonic acid or salts thereof
- D06M11/72—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with phosphorus or compounds thereof, e.g. with chlorophosphonic acid or salts thereof with metaphosphoric acids or their salts; with polyphosphoric acids or their salts; with perphosphoric acids or their salts
-
- 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
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/14—Sulfonic acids or sulfuric acid esters; Salts thereof derived from aliphatic hydrocarbons or mono-alcohols
- C11D1/146—Sulfuric acid esters
-
- 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
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/22—Sulfonic acids or sulfuric acid esters; Salts thereof derived from aromatic compounds
Definitions
- This invention relates to new compositions of matter comprising specific detergent brighteners which are relatively water-insoluble and to processes for preparing dtergent compositions utilizing said new compositions of matter.
- optical brighteners which are relatively insoluble in water are particularly eifective for use in detergent compositions which are used to wash, e.g., such synthetic textiles as nylon and Dacron. It has been discovered that detergent compositions comprising these relatively water-insoluble optical brighteners must contain the optical brightener in a highly dispersed form if maximum deposition of the optical brightner on the article to be cleaned is to be achieved within the short time in which the textile is in the wash solution Hence the optical brighteners must first become solubilized in the aqueous wash solution and then deposit out on the textile.
- the optical brightener is incorporated in the detergent composition in the form of large particles, the rate of solution is too slow and insufficient time is available in the Washing cycle for the brightener to become solubilized in the wash solution and to deposit out on the textiles.
- solid detergent compositions such as spray dried granules
- the brightener be dissolved in such materials as alcohol prior to adding the brightener to the detergent slurry which is subsequently spray dried to form detergent granules. This process involves adding an extraneous material, i.e., the alcohol, to the detergent slurry, which in turn requires that the alcohol be subsequently removed during the spray drying. This method is wasteful.
- composition consisting essentially of (1) a nited States Patent ice solvent selected from the group consisting of (a) an amide in liquid form having the formula i RCN ⁇ wherein 0 ll R-C- is an acyl group containing from about 8 to about 18 carbon atoms and X and Y are each selected from the group consisting of hydrogen, alkyl groups containing from one to about four carbon atoms, and hydroxy alkyl groups containing from one to about three carbon atoms and from one to about two hydroxy groups, (b) a fatty acid in liquid form containing from about 8 to about 31 carbon atoms, and (0) mixtures thereof, and (2) a brightsaid solvent having a temperature of less than about 250 F., said brightener being present in an amount greater than about 0.001% by weight of said solvent up to the limit of the brighteners solubility in the solvent and said brightener being essentially completely dissolved in said solvent.
- a nited States Patent ice solvent selected from the group consisting of (a) an
- the above composition can be utilized in the preparation of granular detergent compositions, especially anionic granular detergent compositions, e.g., by thoroughly mixing from about 0.001% to about 5% by weight, based on the finished granular detergent, of the said composition in an aqueous mixture which is then used to form the said granular detergent compositions by the removal of free moisture.
- the brightener hereinbefore described is representative of relatively water-insoluble brighteners which have particular effectiveness, e.g., when incorporated in detergent compositions which are used to Wash such synthetic textiles as nylon and Dacron.
- the specific brightener hereinbefore mentioned i.e., symmetrical 1,2(5-methyl benzoxazolyl)-ethylene is particularly effective in brightening the aforesaid synthetic textiles as well as other textiles when incorporated into detergent compositions as hereinafter described.
- the solvents in which the brightener of this invention are dissolved are useful and conventional components of detergent compositions.
- Suitable fatty amides include; ammonia amides; N-methyl amides; N-isopropanol amides; N-isobutyl amides; N-ethanol amides; N-diethanol amides; and mixtures of the preceding amides.
- the acyl groups in the above amides contain from about 8 to about 18 carbon atoms, i.e., caprylic, capric, lauric, myristic, palmitic and stearic acyl groups. Mixtures of chain lengths are suitable including acyl groups derived from natural oils such as coconut oil, palm oil, tallow, etc., and mixtures of acyl groups prepared synthetically.
- the acyl groups can be unsaturated as, for example, in oleamide.
- suitable amides and their use in detergent com- 3 positions can be found in US. Patents 2,383,737 and 2,383,738.
- the choice of the specific amide used will depend upon the type of detergent composition desired and the availability of the particular amides. These amides are useful in enhancing the sudsing and detergency of synthetic detergent compositions.
- Suitable fatty acids and their use in detergent compositions include the fatty acid mixtures described in US. Patents 2,954,347 and 2,954,348. These mixtures of myristic, palmitic, stearic, arachidic, behenic, oleic, lignoceric, cerotic, melissic, and linoleic acids i.e., chain lengths from about 14 to about 31 carbon atoms) are used as suds depressants, either alone or in combination with other suds depressants.
- Shorter chain length fatty acids such as those derived from coconut oil and including caprylic, capric, and lauric fatty acids can be used as solvents, but longer chain length fatty acids such as those derived from tallow or hydrogenated fish oils are preferred and are better solvents.
- the fatty acids can be neutralized in the finished product either wholly or in part to form a soap and thereby act as detergent surfactants and/or suds depressants.
- the brightener hereinbefore described is incorporated in the solvents hereinbefore described while the solvents are in a liquid (molten) form. Suitable mixing action is provided to enable the brightener to dissolve in the solvents in a reasonable period of time.
- the incorporation of the brightener in the solvents is achieved relatively easily. From about 0.001% to the solubility limit, usually about 2% by weight, based on the solvent, preferably about 1% by weight, of the brightener is added to the solvents in molten form at a temperature which is less than about 250 F.
- the amount of brightener which can be incorporated in the solvents is related to the temperature of the amide. The higher the temperature the more brightener can be incorporated, but with higher temperatures the solvents undergo degradation reactions. In general, the solvents should be held at as low a temperature as possible While maintaining the solvents in a molten state but maintaining the temperature at a sufiiciently high level to incorporate the desired amount of brightener.
- the above solvent/brightener compositions can be incorporated in a detergent composition in an amount from about 0.001% to about 5% by weight of the detergent composition. Preferably from about .5% to about 3.0% by weight is used and, desirably, about 2% by weight of the solvent/brightener composition is used in the detergent composition.
- the solvent/brightener can be incorporated in the detergent composition by dispersing the solvent/brightener in the aqueous slurry of the composition which is spray dried, drum dried, or dehydrated by the addition of hydrate forming salts to form detergent granules.
- the solvent/brightener composition is normally added to the slurry-containing crutcher and is thereby thoroughly mixed into the granular detergent composition resulting from drying the slurry.
- the brightener is dispersed in extremely finely divided form in the finished granular detergent composition. It is believed that the brightener in the finished detergent composition is in extremely finely divided form approximating a solution.
- the brightener/solvent solution becomes an integral part of a granular detergent composition, it is present in either a solidified form or absorbed as a liquid in the solid granules at ordinary temperatures such as room temperatures, e.g., 60 F.-90 F.
- the detergent surfactant is essentially anionic in character and detergent granules are prepared by forming an aqueous slurry comprising an anionic surfactant.
- the solvent/brightener compositions of this invention posses particular utility.
- the brightener of this invention by itself is relatively insoluble in anionic detergent compounds and in aqueous anionic detergent slurries and consequently, with normal mixing, the brightener is not sutficiently dispersed in the granules, which are subsequently formed from the slurries when the free water is removed, to effect substantial deposition or the brightener on the textiles during a short washing cycle.
- the brightener When the brightener is incorporated in anionic detergent compositions by the solvent/brightener solutions and process of this invention, the brightener is found to be much more effective during fabric laundering than when it is simply added to an anionic detergent-containing crutcher by itself.
- anionic detergent slurries contain about 50% to about 70% solids, the balance being water.
- the solvent/brightener solution can also be added to the detergent composition after the detergent composition is in solid form, e.g., by spraying the molten solvent/ brightener solution onto the finished detergent particles or finished detergent briquettes.
- This latter approach is especially useful when the particular solvent employed is of the type which does not readily withstand the elevated temperatures associated with spray drying, e.g., highly unsaturated fatty acids, or when the detergent surfactant or other ingredients cannot be spray dried.
- the amount of brightener in the finished detergent composition will range from about .00l% to about .1 by weight of the detergent composition, preferably from about .0l% to about .03% by weight and most preferably at .02% by weight of the composition.
- the solvents of this invention containing the brighteners of this invention can be used in combination with a variety of detergent actives in forming detergent compositions.
- Suitable detergent surfactants which can be used in amounts from about 5% to about 50% by weight of the detergent composition in these detergent compositions include: synthetic organic detergents characterized by their high solubility in water, their resistance to preclpitation by the constituents of hard Water and their surface active and effective detergent properties, including: I
- Anionic synthetic detergents can be broadly described as the water-soluble salts, particularly the alkali metal salts, of organic sulfuric reaction products having in the molecular structure an alkyl radical containing from about 8 to about 22 carbon atoms and a radical selected from the group consisting of sulfonic acid and sulfuric acid ester radicals.
- the synthetic detergents WhICh form a part of the preferred compositions of the present 1nvention are the sodium or potassium alkyl sulfates, especially those obtained by sulfating the higher alcohols produced by reducing the glycerides of tallow or coconut oil; sodium or potassium alkyl benzene sulfonates, in which the alkyl group is a straight or branched chain containing from about 9 to about 15 carbon atoms, especially those of the types described in United States Letters Patent Nos.
- a higher fatty alcohol e.g., tallow or coconut oil alcohols
- fatty acids are derived from coconut oil; sodium or potassium salts of fatty acid amide of a methyl taurine in which the fatty acids, for example, are derived from coconut oil; and others known in the art, a number being specifically set forth in United States Letters Patent Nos. 2,486,921, 2,486,922 and 2,396,278.
- the alkyl groups contained in said detergent surfactants can be straight or branched and saturated or un saturated as desired.
- the above list of detergent SUI- factants is exemplary and not limiting. Mixtures of the above detergent surfactants with themselves and with other detergent surfactants can be used.
- Sodium and potassium alkyl sulfates and/or alkyl benzene sulfonates as hereinbefore described are particularly desirable, especially in spray dried detergent granules. They can be used together in ratios of 3:1 to 1:3, preferably 55 parts sulfonate to 45 parts sulfate.
- the detergent compositions can also contain from about 5% to about 90% by weight of the detergent composition of detergency builders.
- detergency builders are preferably used in this percentage range in a sufiicient amount to provide a ratio of detergency builder to detergent surfactant of from about 1:1 to about 8:1 on a weight basis.
- water-soluble inorganic alkaline detergency builder salts are alkali metal carbonates, phosphates, polyphosphates, and silicates. Specific examples of such salts are sodium and potassium tripolyphosphates, carbonates, pyrophosphates, phosphates, and hexametaphosphates.
- organic alkaline sequestrant builder salts are (1) alkali metal amino polycarboxylates [e.g., sodium and potassium ethylene diaminetetraacetates, N-(Z-hydroxyethyl) ethylenediamine, triacetates, nitrilotriacetates, and N-(Z-hydroxyethyl)-nitrilo diacetates]; (2) alkali metal salts of phytic acid (e.g., sodium and potassium phytates-see US.
- alkali metal amino polycarboxylates e.g., sodium and potassium ethylene diaminetetraacetates, N-(Z-hydroxyethyl) ethylenediamine, triacetates, nitrilotriacetates, and N-(Z-hydroxyethyl)-nitrilo diacetates
- alkali metal salts of phytic acid e.g., sodium and potassium phytates-see US.
- Patent 2,739,942 water-soluble salts of ethane-l-hydroxy- 1,1-diphosphonate (e.g., the trisodium and tripotassium salts); (4) water-soluble salts of methylene diphosphonic acid (e.g., trisodium and tripotassium methylene diphosphonate and the other salts described in the copending application of Francis L. Diehl, Ser. No. 266,025, filed Mar. 18, 1963, now Patent No.
- methylene diphosphonic acid e.g., trisodium and tripotassium methylene diphosphonate and the other salts described in the copending application of Francis L. Diehl, Ser. No. 266,025, filed Mar. 18, 1963, now Patent No.
- 3,308,067 e.g., polymers of itaconic acid, aconitic acid, maleic acid, mesaconic acid, fumaric acid, methylene malonic acid, and citronic acid and copolymers with themselves and other compatible monomers such as ethylene; and (7) mixtures thereof.
- Mixtures of organic and/ or inorganic builders can be used and are generally desirable. Especially preferred are the mixtures of builders disclosed in the copending application of Burton H. Gedge, Ser. No. 235,327, filed Nov. 5, 1962, now Patent No. 3,392,121, e.g., ternary mixtures of sodium tripolyphosphate, sodium nitrolotriacetate, and sodium ethane-1-hydroxy1,l-diphosphonate.
- minor ingredients can also be added, if desired, to the detergent compositions which are prepared using the amide-brightener composition of this invention.
- Such minor ingredients include soil suspending agents such as carboxymethylcellulose, sodium and potassium silicates, diluents such as sodium sulfate and sodium chloride, dye and benzotriazole.
- the total amount of these minor ingredients is preferably less than about 10% by weight of the detergent composition, but can be used in greater amounts if necessary to form the balance of the composition.
- the detergent surfactant, the builders and the minor ingredients are incorporated into the detergent granule but they can also be added individually in the form of particles.
- Percent Sodium tripolyphosphate 46.5 Sodium straight chain alkyl benzene sulfonate wherein the alkyl group distribution is about 10%C10; 35%C11; 25%-C12; 23%-C13; 2%C and about 5% branched chain components which were not characterized as to chain length 17.5 Sodium toluene sulfonate 2 Sodium sulfate 15 Sodium silicate having a ratio of SiO :Na O of 1.6 5.9 Amide/brightener composition in the amount required to provide about 2.1% amide and about .02% optical brightener 2.1 Moisture 10 parts of the above ingredients were added to a crutcher in the proportions indicated and mixed together with an additional approximately 40 parts water.
- detergent granules of the above composition and moisture content were especially effective in that the optical brightener was dispersed through said detergent granules in a highly dispersed form and, accordingly, the optical brightener was effectively deposited on synthetic textiles such as nylon and Dacron when the detergent granules were used to wash said textiles.
- the amide acted as a sudsing and detergency enhancing agent for the granular detergent.
- EXAMPLE II About 1% by weight of the brightener of Example I is dissolved at about 200 F. in a mixture of fatty acids in liquid form consisting of 8% myristic acid, 29% palmitic acid, 18% stearic acid, 26% arachidic acid, 17% behenic acid, and 2% oleic acid to form a useful composition. Similarly tallow and/or coconut fatty acids can be substituted either wholly or in part for the above fatty acids to prepare useful compositions.
- miscellaneous ingredients including water of hydration, sodium sulfate, etc., and about 16% sodium carbonate.
- the alkalinity of this composition converts added fatty acid into corresponding sodium soap, but without affecting the brightener or its finely dispersed character.
- the above detergent compositions are excellent for laundering and cleaning, e.g., textiles such as nylon and Dacron and contain brightener in a highly dispersed form which is effective in despositing upon and optically brightening said textiles.
- said brightener being present in an amount greater than about 0.001% by weight of said fatty acid solvent up to the limit of said bn'ghteners solubility in the fatty acid solvent and spraying said mixture at a temperature of less than 250 F. onto a granular mixture consisting essentially of (C) 'an anionic synthetic detergent surfactant selected from the group consisting of sodium and potassium alkyl sulfates wherein the alkyl group contains 8 to 22 carbon atoms, alkylbenzenesulfonates wherein the alkyl group contains 9 to 15 carbon atoms and mixtures thereof, in an amount sufiicient to give from about 5% to about anionic synthetic detergent surfactant in the finished granular anionic detergent, and
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Description
U.S. Cl. 252110 2 Claims ABSTRACT OF THE DISCLOSURE A process for producing an anionic detergent composition with brightening properties by spraying a mixture of a relatively waterinsoluble brightener dispersed in fatty acids onto a granular anionic detergent mixture.
This is a continuation of a pending application Ser. No. 375,326, filed June 15, 1964, now abandoned.
This invention relates to new compositions of matter comprising specific detergent brighteners which are relatively water-insoluble and to processes for preparing dtergent compositions utilizing said new compositions of matter.
Certain optical brighteners which are relatively insoluble in water are particularly eifective for use in detergent compositions which are used to wash, e.g., such synthetic textiles as nylon and Dacron. It has been discovered that detergent compositions comprising these relatively water-insoluble optical brighteners must contain the optical brightener in a highly dispersed form if maximum deposition of the optical brightner on the article to be cleaned is to be achieved within the short time in which the textile is in the wash solution Apparently the optical brighteners must first become solubilized in the aqueous wash solution and then deposit out on the textile. If the optical brightener is incorporated in the detergent composition in the form of large particles, the rate of solution is too slow and insufficient time is available in the Washing cycle for the brightener to become solubilized in the wash solution and to deposit out on the textiles. In order to disperse these relatively Water-insoluble brighteners in solid detergent compositions such as spray dried granules it has been suggested that the brightener be dissolved in such materials as alcohol prior to adding the brightener to the detergent slurry which is subsequently spray dried to form detergent granules. This process involves adding an extraneous material, i.e., the alcohol, to the detergent slurry, which in turn requires that the alcohol be subsequently removed during the spray drying. This method is wasteful.
It is an object of this invention to provide a composition comprising a relatively water-insoluble optical brightener in solubilized form suitable for incorporation in detergent compositions.
It is a further object of this invention to provide an efiicient process for incorporating relatively insoluble optical brighteners into detergent compositions.
These objects and other objects can be achieved by providing a. composition consisting essentially of (1) a nited States Patent ice solvent selected from the group consisting of (a) an amide in liquid form having the formula i RCN\ wherein 0 ll R-C- is an acyl group containing from about 8 to about 18 carbon atoms and X and Y are each selected from the group consisting of hydrogen, alkyl groups containing from one to about four carbon atoms, and hydroxy alkyl groups containing from one to about three carbon atoms and from one to about two hydroxy groups, (b) a fatty acid in liquid form containing from about 8 to about 31 carbon atoms, and (0) mixtures thereof, and (2) a brightsaid solvent having a temperature of less than about 250 F., said brightener being present in an amount greater than about 0.001% by weight of said solvent up to the limit of the brighteners solubility in the solvent and said brightener being essentially completely dissolved in said solvent.
The above composition can be utilized in the preparation of granular detergent compositions, especially anionic granular detergent compositions, e.g., by thoroughly mixing from about 0.001% to about 5% by weight, based on the finished granular detergent, of the said composition in an aqueous mixture which is then used to form the said granular detergent compositions by the removal of free moisture.
The brightener hereinbefore described is representative of relatively water-insoluble brighteners which have particular effectiveness, e.g., when incorporated in detergent compositions which are used to Wash such synthetic textiles as nylon and Dacron. The specific brightener hereinbefore mentioned, i.e., symmetrical 1,2(5-methyl benzoxazolyl)-ethylene is particularly effective in brightening the aforesaid synthetic textiles as well as other textiles when incorporated into detergent compositions as hereinafter described.
The solvents in which the brightener of this invention are dissolved are useful and conventional components of detergent compositions.
Examples of suitable fatty amides include; ammonia amides; N-methyl amides; N-isopropanol amides; N-isobutyl amides; N-ethanol amides; N-diethanol amides; and mixtures of the preceding amides. The acyl groups in the above amides contain from about 8 to about 18 carbon atoms, i.e., caprylic, capric, lauric, myristic, palmitic and stearic acyl groups. Mixtures of chain lengths are suitable including acyl groups derived from natural oils such as coconut oil, palm oil, tallow, etc., and mixtures of acyl groups prepared synthetically. The acyl groups can be unsaturated as, for example, in oleamide. Further examples of suitable amides and their use in detergent com- 3 positions can be found in US. Patents 2,383,737 and 2,383,738. The choice of the specific amide used will depend upon the type of detergent composition desired and the availability of the particular amides. These amides are useful in enhancing the sudsing and detergency of synthetic detergent compositions.
Examples of suitable fatty acids and their use in detergent compositions include the fatty acid mixtures described in US. Patents 2,954,347 and 2,954,348. These mixtures of myristic, palmitic, stearic, arachidic, behenic, oleic, lignoceric, cerotic, melissic, and linoleic acids i.e., chain lengths from about 14 to about 31 carbon atoms) are used as suds depressants, either alone or in combination with other suds depressants. Shorter chain length fatty acids such as those derived from coconut oil and including caprylic, capric, and lauric fatty acids can be used as solvents, but longer chain length fatty acids such as those derived from tallow or hydrogenated fish oils are preferred and are better solvents. The fatty acids can be neutralized in the finished product either wholly or in part to form a soap and thereby act as detergent surfactants and/or suds depressants.
The brightener hereinbefore described is incorporated in the solvents hereinbefore described while the solvents are in a liquid (molten) form. Suitable mixing action is provided to enable the brightener to dissolve in the solvents in a reasonable period of time. The incorporation of the brightener in the solvents is achieved relatively easily. From about 0.001% to the solubility limit, usually about 2% by weight, based on the solvent, preferably about 1% by weight, of the brightener is added to the solvents in molten form at a temperature which is less than about 250 F. The amount of brightener which can be incorporated in the solvents is related to the temperature of the amide. The higher the temperature the more brightener can be incorporated, but with higher temperatures the solvents undergo degradation reactions. In general, the solvents should be held at as low a temperature as possible While maintaining the solvents in a molten state but maintaining the temperature at a sufiiciently high level to incorporate the desired amount of brightener.
The above solvent/brightener compositions can be incorporated in a detergent composition in an amount from about 0.001% to about 5% by weight of the detergent composition. Preferably from about .5% to about 3.0% by weight is used and, desirably, about 2% by weight of the solvent/brightener composition is used in the detergent composition. The solvent/brightener can be incorporated in the detergent composition by dispersing the solvent/brightener in the aqueous slurry of the composition which is spray dried, drum dried, or dehydrated by the addition of hydrate forming salts to form detergent granules. The solvent/brightener composition is normally added to the slurry-containing crutcher and is thereby thoroughly mixed into the granular detergent composition resulting from drying the slurry. By this method the brightener is dispersed in extremely finely divided form in the finished granular detergent composition. It is believed that the brightener in the finished detergent composition is in extremely finely divided form approximating a solution. When the brightener/solvent solution becomes an integral part of a granular detergent composition, it is present in either a solidified form or absorbed as a liquid in the solid granules at ordinary temperatures such as room temperatures, e.g., 60 F.-90 F.
When the detergent surfactant is essentially anionic in character and detergent granules are prepared by forming an aqueous slurry comprising an anionic surfactant. as hereinbefore described, the solvent/brightener compositions of this invention posses particular utility. The brightener of this invention by itself is relatively insoluble in anionic detergent compounds and in aqueous anionic detergent slurries and consequently, with normal mixing, the brightener is not sutficiently dispersed in the granules, which are subsequently formed from the slurries when the free water is removed, to effect substantial deposition or the brightener on the textiles during a short washing cycle. When the brightener is incorporated in anionic detergent compositions by the solvent/brightener solutions and process of this invention, the brightener is found to be much more effective during fabric laundering than when it is simply added to an anionic detergent-containing crutcher by itself. Usually anionic detergent slurries contain about 50% to about 70% solids, the balance being water.
The solvent/brightener solution can also be added to the detergent composition after the detergent composition is in solid form, e.g., by spraying the molten solvent/ brightener solution onto the finished detergent particles or finished detergent briquettes. This latter approach is especially useful when the particular solvent employed is of the type which does not readily withstand the elevated temperatures associated with spray drying, e.g., highly unsaturated fatty acids, or when the detergent surfactant or other ingredients cannot be spray dried.
The amount of brightener in the finished detergent composition will range from about .00l% to about .1 by weight of the detergent composition, preferably from about .0l% to about .03% by weight and most preferably at .02% by weight of the composition.
The solvents of this invention containing the brighteners of this invention can be used in combination with a variety of detergent actives in forming detergent compositions. Suitable detergent surfactants which can be used in amounts from about 5% to about 50% by weight of the detergent composition in these detergent compositions include: synthetic organic detergents characterized by their high solubility in water, their resistance to preclpitation by the constituents of hard Water and their surface active and effective detergent properties, including: I
Anionic synthetic detergents. This class of synthetic detergents can be broadly described as the water-soluble salts, particularly the alkali metal salts, of organic sulfuric reaction products having in the molecular structure an alkyl radical containing from about 8 to about 22 carbon atoms and a radical selected from the group consisting of sulfonic acid and sulfuric acid ester radicals. Important examples of the synthetic detergents WhICh form a part of the preferred compositions of the present 1nvention are the sodium or potassium alkyl sulfates, especially those obtained by sulfating the higher alcohols produced by reducing the glycerides of tallow or coconut oil; sodium or potassium alkyl benzene sulfonates, in which the alkyl group is a straight or branched chain containing from about 9 to about 15 carbon atoms, especially those of the types described in United States Letters Patent Nos. 2,220,099 and 2,477,383; sulfonated alpha olefins containing from about 12 to about 18 carbon atoms, sodium alkyl glyceryl ether sulfonates, especially those ethers of the higher alcohols derived from tallow and coconut oil; sodium coconut oil fatty acid monoglyceride sulfates and sulfonates; sodium or potassium salts of sulfuric acid esters of the reaction product of one mole of a higher fatty alcohol (e.g., tallow or coconut oil alcohols) and about three moles of ethylene oxide: sodium or potassium salts of alkyl phenol ethylene oxide ether sulfate with about four units of ethylene oxide per molecule and in which the alkyl radicals contain about 9 carbon atoms; the reaction product of fatty acids esterified. with isethionic acid and neutralized with sodium hydroxide where, for example, the fatty acids are derived from coconut oil; sodium or potassium salts of fatty acid amide of a methyl taurine in which the fatty acids, for example, are derived from coconut oil; and others known in the art, a number being specifically set forth in United States Letters Patent Nos. 2,486,921, 2,486,922 and 2,396,278.
The alkyl groups contained in said detergent surfactants can be straight or branched and saturated or un saturated as desired. The above list of detergent SUI- factants is exemplary and not limiting. Mixtures of the above detergent surfactants with themselves and with other detergent surfactants can be used. Sodium and potassium alkyl sulfates and/or alkyl benzene sulfonates as hereinbefore described are particularly desirable, especially in spray dried detergent granules. They can be used together in ratios of 3:1 to 1:3, preferably 55 parts sulfonate to 45 parts sulfate.
In addition to the above mentioned ingredients the detergent compositions can also contain from about 5% to about 90% by weight of the detergent composition of detergency builders. These detergency builders are preferably used in this percentage range in a sufiicient amount to provide a ratio of detergency builder to detergent surfactant of from about 1:1 to about 8:1 on a weight basis. Examples of water-soluble inorganic alkaline detergency builder salts are alkali metal carbonates, phosphates, polyphosphates, and silicates. Specific examples of such salts are sodium and potassium tripolyphosphates, carbonates, pyrophosphates, phosphates, and hexametaphosphates. Examples of organic alkaline sequestrant builder salts are (1) alkali metal amino polycarboxylates [e.g., sodium and potassium ethylene diaminetetraacetates, N-(Z-hydroxyethyl) ethylenediamine, triacetates, nitrilotriacetates, and N-(Z-hydroxyethyl)-nitrilo diacetates]; (2) alkali metal salts of phytic acid (e.g., sodium and potassium phytates-see US. Patent 2,739,942); (3) water-soluble salts of ethane-l-hydroxy- 1,1-diphosphonate (e.g., the trisodium and tripotassium salts); (4) water-soluble salts of methylene diphosphonic acid (e.g., trisodium and tripotassium methylene diphosphonate and the other salts described in the copending application of Francis L. Diehl, Ser. No. 266,025, filed Mar. 18, 1963, now Patent No. 3,213,030); (5) watersoluble salts of substituted methylene diphosphonic acids (e.g., trisodium and tripotassium ethylidene, isopropylidene, benzylmethylidene, and halomethylidene diphosphonates and the other substituted methylene diphosphonates disclosed in the copending application of Clarence H. Roy, Ser. No. 266,055, filed Mar. 18, 1963, now Patent No. 3,422,021); (6) water-soluble salts of polycarboxylate polymers and copolymers as described in the copending application of Francis L. Diehl, Ser. No. 269,359, filed Apr. 1, 1963, now Patent No. 3,308,067 (e.g., polymers of itaconic acid, aconitic acid, maleic acid, mesaconic acid, fumaric acid, methylene malonic acid, and citronic acid and copolymers with themselves and other compatible monomers such as ethylene); and (7) mixtures thereof.
Mixtures of organic and/ or inorganic builders can be used and are generally desirable. Especially preferred are the mixtures of builders disclosed in the copending application of Burton H. Gedge, Ser. No. 235,327, filed Nov. 5, 1962, now Patent No. 3,392,121, e.g., ternary mixtures of sodium tripolyphosphate, sodium nitrolotriacetate, and sodium ethane-1-hydroxy1,l-diphosphonate.
Other minor ingredients can also be added, if desired, to the detergent compositions which are prepared using the amide-brightener composition of this invention. Such minor ingredients include soil suspending agents such as carboxymethylcellulose, sodium and potassium silicates, diluents such as sodium sulfate and sodium chloride, dye and benzotriazole. The total amount of these minor ingredients is preferably less than about 10% by weight of the detergent composition, but can be used in greater amounts if necessary to form the balance of the composition.
Normally the detergent surfactant, the builders and the minor ingredients are incorporated into the detergent granule but they can also be added individually in the form of particles.
All percentages, ratios, and parts herein are by Weight unless otherwise specified.
The following examples demonstrate the desirable and unique compositions and processes of this invention.
6 EXAMPLE I About 1% by weight, based on the solvent/brightener composition, of symmetrical 1,2(5-methylbenzoxazolyl) ethylene was dissolved in middle cut coconut N-monoethanol amide wherein the acyl groups in said amide had a distribution such that 2% were C 66% were C 23% were C and 9% were C The amide was held at a temperature of about 200 F. while the optical brightener was being dissolved with mixing in the amide. This amide-brightener composition was used in preparing a granular detergent composition having the following formula:
Percent Sodium tripolyphosphate 46.5 Sodium straight chain alkyl benzene sulfonate wherein the alkyl group distribution is about 10%C10; 35%C11; 25%-C12; 23%-C13; 2%C and about 5% branched chain components which were not characterized as to chain length 17.5 Sodium toluene sulfonate 2 Sodium sulfate 15 Sodium silicate having a ratio of SiO :Na O of 1.6 5.9 Amide/brightener composition in the amount required to provide about 2.1% amide and about .02% optical brightener 2.1 Moisture 10 parts of the above ingredients were added to a crutcher in the proportions indicated and mixed together with an additional approximately 40 parts water. After the ingredients were thoroughly mixed together they were spray dried by conventional means into detergent granules of the above composition and moisture content. These detergent granules were especially effective in that the optical brightener was dispersed through said detergent granules in a highly dispersed form and, accordingly, the optical brightener was effectively deposited on synthetic textiles such as nylon and Dacron when the detergent granules were used to wash said textiles. The amide acted as a sudsing and detergency enhancing agent for the granular detergent.
When middle cut coconut or tallow N-diethanol, ammonia, N methyl, N dimethyl, N ethyl, N- diethyl, N-propyl, N-diisopropyl, N-isobutyl, N-dibutyl, 'N-glycerol, N-diglycerol, N-methanol, and N-dimethanol amides or mixtures thereof are substituted either Wholly or in part for the coconut N-monoethanol amide in the above example, substantially equivalent results are obtained in that the brightener is solubilized in the amide and is contained in the finished granular anionic detergent in a highly dispersed form and gives maximum deposition on washed fabrics.
When sodium or potassium alkyl sulfates derived from, e.g., tallow alcohols are substituted either wholly or in part (e.g., about 45%) for the sodium alkyl benzene sulfonate in the above example, substantially equivalent results are obtained in that the detergent granules contain the brightener in a highly dispersed form.
EXAMPLE II About 1% by weight of the brightener of Example I is dissolved at about 200 F. in a mixture of fatty acids in liquid form consisting of 8% myristic acid, 29% palmitic acid, 18% stearic acid, 26% arachidic acid, 17% behenic acid, and 2% oleic acid to form a useful composition. Similarly tallow and/or coconut fatty acids can be substituted either wholly or in part for the above fatty acids to prepare useful compositions.
About 3 parts of the above fatty acid/brightener compositions are added, by spraying, to 97 parts of a granular mixtures of about 17% potassium alkyl (C average) benzene sulfonate, about 43% sodium tripolyphosphate, about 6% sodium silicate solids (1.621 sio zNa O),
and 18% of miscellaneous ingredients including water of hydration, sodium sulfate, etc., and about 16% sodium carbonate. The alkalinity of this composition converts added fatty acid into corresponding sodium soap, but without affecting the brightener or its finely dispersed character.
When the above ingredients, including the fatty acid/ brightener compositions, are added to a detergent slurry in a crutcher with 40 parts of additional water, mixed together, and spray dried by conventional means to form detergent granules, essentially equivalent results are obtained in that the brightener is found in said detergent granules in a highly dispersed and particularly effective form.
The above detergent compositions are excellent for laundering and cleaning, e.g., textiles such as nylon and Dacron and contain brightener in a highly dispersed form which is effective in despositing upon and optically brightening said textiles.
What is claimed is:
1. The process of preparing a granular anionic detergent comprising the step of forming from about 0.001% to about by weight, based on the finished granular detergent, of a mixture of (A) a fatty acid in liquid form containing from about 8 to 31 carbon atoms and (B) a brightener having the formula I CCH=CHC CH,
said brightener being present in an amount greater than about 0.001% by weight of said fatty acid solvent up to the limit of said bn'ghteners solubility in the fatty acid solvent and spraying said mixture at a temperature of less than 250 F. onto a granular mixture consisting essentially of (C) 'an anionic synthetic detergent surfactant selected from the group consisting of sodium and potassium alkyl sulfates wherein the alkyl group contains 8 to 22 carbon atoms, alkylbenzenesulfonates wherein the alkyl group contains 9 to 15 carbon atoms and mixtures thereof, in an amount sufiicient to give from about 5% to about anionic synthetic detergent surfactant in the finished granular anionic detergent, and
(D) a water-soluble alkaline detergency builder material, the ratio of said detergency builder to said detergent surfactant being about 1:1 to about 8:1, whereby the alkalinity of the granular mixture converts fatty acid into the corresponding soap without affecting the brightener or its finely dispersed character.
2. The process of claim 1 wherein the granular mixture consists essentially of potassium alkylbenzenesulfomate and sodium tripolyphosphate.
References Cited UNITED STATES PATENTS 5/1961 Siegrist 252-3012 12/1967 Hausermann 260-310 US. Cl. X.R.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US61619567A | 1967-02-15 | 1967-02-15 |
Publications (1)
Publication Number | Publication Date |
---|---|
US3485761A true US3485761A (en) | 1969-12-23 |
Family
ID=24468411
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US616195A Expired - Lifetime US3485761A (en) | 1967-02-15 | 1967-02-15 | Production of detergent compositions containing finely dispersed optical brighteners |
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US (1) | US3485761A (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3650816A (en) * | 1969-05-02 | 1972-03-21 | Lever Brothers Ltd | Additives for clothes dryers |
US3849162A (en) * | 1971-06-07 | 1974-11-19 | Ciba Geigy Ag | Process for preventing the staining of polyamide fibre material treated with fluorescent whiteners |
US3900608A (en) * | 1971-10-23 | 1975-08-19 | Bayer Ag | Preparations of optical brighteners |
US4008166A (en) * | 1973-09-05 | 1977-02-15 | Ciba-Geigy Corporation | Optically brightening with a synergistic mixture |
US4058480A (en) * | 1973-09-14 | 1977-11-15 | Ciba-Geigy Corporation | Non-dusting, readily free-flowing granules of optical brighteners |
US4235597A (en) * | 1975-11-27 | 1980-11-25 | Ciba-Geigy Corporation | Granules of textile processing agents for use in organic solvent liquors |
US4252664A (en) * | 1978-10-30 | 1981-02-24 | Colgate-Palmolive Company | Effervescent granules |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2986528A (en) * | 1956-03-16 | 1961-05-30 | Ciba Ltd | Method of optically brightening organic materials and preparations therefor |
US3357988A (en) * | 1964-05-27 | 1967-12-12 | Geigy Chem Corp | Pyrazoline optical brighteners |
-
1967
- 1967-02-15 US US616195A patent/US3485761A/en not_active Expired - Lifetime
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2986528A (en) * | 1956-03-16 | 1961-05-30 | Ciba Ltd | Method of optically brightening organic materials and preparations therefor |
US3357988A (en) * | 1964-05-27 | 1967-12-12 | Geigy Chem Corp | Pyrazoline optical brighteners |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3650816A (en) * | 1969-05-02 | 1972-03-21 | Lever Brothers Ltd | Additives for clothes dryers |
US3849162A (en) * | 1971-06-07 | 1974-11-19 | Ciba Geigy Ag | Process for preventing the staining of polyamide fibre material treated with fluorescent whiteners |
US3900608A (en) * | 1971-10-23 | 1975-08-19 | Bayer Ag | Preparations of optical brighteners |
US4008166A (en) * | 1973-09-05 | 1977-02-15 | Ciba-Geigy Corporation | Optically brightening with a synergistic mixture |
US4058480A (en) * | 1973-09-14 | 1977-11-15 | Ciba-Geigy Corporation | Non-dusting, readily free-flowing granules of optical brighteners |
US4235597A (en) * | 1975-11-27 | 1980-11-25 | Ciba-Geigy Corporation | Granules of textile processing agents for use in organic solvent liquors |
US4252664A (en) * | 1978-10-30 | 1981-02-24 | Colgate-Palmolive Company | Effervescent granules |
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