US3560391A - Detergent compositions containing phosphonio carboxylates - Google Patents
Detergent compositions containing phosphonio carboxylates Download PDFInfo
- Publication number
- US3560391A US3560391A US5900*[A US3560391DA US3560391A US 3560391 A US3560391 A US 3560391A US 3560391D A US3560391D A US 3560391DA US 3560391 A US3560391 A US 3560391A
- Authority
- US
- United States
- Prior art keywords
- phosphonio
- detergent
- sodium
- builder
- compositions
- 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 abstract description 78
- 239000003599 detergent Substances 0.000 title abstract description 77
- MEUIIHOXOWVKNP-UHFFFAOYSA-N phosphanylformic acid Chemical class OC(P)=O MEUIIHOXOWVKNP-UHFFFAOYSA-N 0.000 title description 33
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 49
- 150000001875 compounds Chemical class 0.000 abstract description 45
- -1 PHOSPHONIO CARBOXYLATES Chemical class 0.000 abstract description 37
- 150000003839 salts Chemical class 0.000 abstract description 26
- 239000000463 material Substances 0.000 abstract description 18
- 238000004900 laundering Methods 0.000 abstract description 9
- 239000003352 sequestering agent Substances 0.000 abstract description 9
- 238000000034 method Methods 0.000 abstract description 6
- 238000005406 washing Methods 0.000 description 24
- 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 23
- 239000011734 sodium Substances 0.000 description 23
- 235000015424 sodium Nutrition 0.000 description 23
- 229910052708 sodium Inorganic materials 0.000 description 22
- 239000004744 fabric Substances 0.000 description 18
- 238000004140 cleaning Methods 0.000 description 16
- 239000007788 liquid Substances 0.000 description 14
- 239000000243 solution Substances 0.000 description 13
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 10
- 125000004432 carbon atom Chemical group C* 0.000 description 10
- FERIUCNNQQJTOY-UHFFFAOYSA-M Butyrate Chemical compound CCCC([O-])=O FERIUCNNQQJTOY-UHFFFAOYSA-M 0.000 description 9
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Natural products CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 9
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 9
- 125000000217 alkyl group Chemical group 0.000 description 9
- 239000011591 potassium Substances 0.000 description 9
- 229910052700 potassium Inorganic materials 0.000 description 9
- 235000007686 potassium Nutrition 0.000 description 9
- 235000019832 sodium triphosphate Nutrition 0.000 description 9
- 239000007864 aqueous solution Substances 0.000 description 8
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 6
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
- 239000004115 Sodium Silicate Substances 0.000 description 6
- 239000004615 ingredient Substances 0.000 description 6
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 6
- 229910052911 sodium silicate Inorganic materials 0.000 description 6
- 239000002689 soil Substances 0.000 description 6
- 239000003760 tallow Substances 0.000 description 6
- 229910052783 alkali metal Inorganic materials 0.000 description 5
- 125000000129 anionic group Chemical group 0.000 description 5
- 239000012459 cleaning agent Substances 0.000 description 5
- 239000007859 condensation product Substances 0.000 description 5
- 159000000001 potassium salts Chemical class 0.000 description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 4
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 4
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 4
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 4
- XYFCBTPGUUZFHI-UHFFFAOYSA-N phosphine group Chemical group P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 description 4
- 239000000344 soap Substances 0.000 description 4
- 239000007916 tablet composition Substances 0.000 description 4
- 229920000742 Cotton Polymers 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 150000001340 alkali metals Chemical class 0.000 description 3
- 125000001246 bromo group Chemical group Br* 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 125000001309 chloro group Chemical group Cl* 0.000 description 3
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 3
- FODHIQQNHOPUKH-UHFFFAOYSA-N tetrapropylene-benzenesulfonic acid Chemical compound CC1CC11C2=C3S(=O)(=O)OC(C)CC3=C3C(C)CC3=C2C1C FODHIQQNHOPUKH-UHFFFAOYSA-N 0.000 description 3
- GSEJCLTVZPLZKY-UHFFFAOYSA-O triethanolammonium Chemical compound OCC[NH+](CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-O 0.000 description 3
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 3
- HFDVRLIODXPAHB-UHFFFAOYSA-N 1-tetradecene Chemical compound CCCCCCCCCCCCC=C HFDVRLIODXPAHB-UHFFFAOYSA-N 0.000 description 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 2
- 125000002252 acyl group Chemical group 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- 150000008045 alkali metal halides Chemical class 0.000 description 2
- 150000008051 alkyl sulfates Chemical class 0.000 description 2
- 150000003863 ammonium salts Chemical class 0.000 description 2
- 150000007942 carboxylates Chemical class 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 235000019864 coconut oil Nutrition 0.000 description 2
- 239000003240 coconut oil Substances 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 2
- YRIUSKIDOIARQF-UHFFFAOYSA-N dodecyl benzenesulfonate Chemical compound CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 YRIUSKIDOIARQF-UHFFFAOYSA-N 0.000 description 2
- 229940071161 dodecylbenzenesulfonate Drugs 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 125000001421 myristyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 235000021317 phosphate Nutrition 0.000 description 2
- 229910000073 phosphorus hydride Inorganic materials 0.000 description 2
- 239000001103 potassium chloride Substances 0.000 description 2
- 235000011164 potassium chloride Nutrition 0.000 description 2
- GHKGUEZUGFJUEJ-UHFFFAOYSA-M potassium;4-methylbenzenesulfonate Chemical compound [K+].CC1=CC=C(S([O-])(=O)=O)C=C1 GHKGUEZUGFJUEJ-UHFFFAOYSA-M 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 description 2
- 235000017550 sodium carbonate Nutrition 0.000 description 2
- 159000000000 sodium salts Chemical class 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 150000003871 sulfonates Chemical class 0.000 description 2
- 239000000271 synthetic detergent Substances 0.000 description 2
- RYCLIXPGLDDLTM-UHFFFAOYSA-J tetrapotassium;phosphonato phosphate Chemical compound [K+].[K+].[K+].[K+].[O-]P([O-])(=O)OP([O-])([O-])=O RYCLIXPGLDDLTM-UHFFFAOYSA-J 0.000 description 2
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 2
- 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 2
- 239000003981 vehicle Substances 0.000 description 2
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 1
- CRSBERNSMYQZNG-UHFFFAOYSA-N 1 -dodecene Natural products CCCCCCCCCCC=C CRSBERNSMYQZNG-UHFFFAOYSA-N 0.000 description 1
- XBRSMICTSWBNTP-UHFFFAOYSA-N 1,1,3-triphosphonopropan-2-ylphosphonic acid Chemical compound OP(O)(=O)CC(P(O)(O)=O)C(P(O)(O)=O)P(O)(O)=O XBRSMICTSWBNTP-UHFFFAOYSA-N 0.000 description 1
- OGTPNDHOHCFDTK-UHFFFAOYSA-N 1,2,3-triphosphonopropan-2-ylphosphonic acid Chemical compound OP(O)(=O)CC(P(O)(O)=O)(P(O)(O)=O)CP(O)(O)=O OGTPNDHOHCFDTK-UHFFFAOYSA-N 0.000 description 1
- SFRLSTJPMFGBDP-UHFFFAOYSA-N 1,2-diphosphonoethylphosphonic acid Chemical class OP(O)(=O)CC(P(O)(O)=O)P(O)(O)=O SFRLSTJPMFGBDP-UHFFFAOYSA-N 0.000 description 1
- YVPHSTVRTGSOSK-UHFFFAOYSA-N 1,3,3-triphosphonopropylphosphonic acid Chemical compound OP(O)(=O)C(P(O)(O)=O)CC(P(O)(O)=O)P(O)(O)=O YVPHSTVRTGSOSK-UHFFFAOYSA-N 0.000 description 1
- SIDULKZCBGMXJL-UHFFFAOYSA-N 1-dimethylphosphoryldodecane Chemical compound CCCCCCCCCCCCP(C)(C)=O SIDULKZCBGMXJL-UHFFFAOYSA-N 0.000 description 1
- CJPDBKNETSCHCH-UHFFFAOYSA-N 1-methylsulfinyldodecane Chemical compound CCCCCCCCCCCCS(C)=O CJPDBKNETSCHCH-UHFFFAOYSA-N 0.000 description 1
- MZQKADNPDLDGJD-UHFFFAOYSA-N 2,3,4,5-tetrapropylbenzenesulfonic acid Chemical compound CCCC1=CC(S(O)(=O)=O)=C(CCC)C(CCC)=C1CCC MZQKADNPDLDGJD-UHFFFAOYSA-N 0.000 description 1
- XSXWOBXNYNULJG-UHFFFAOYSA-N 2-(2,4,4-trimethylpentan-2-yl)phenol Chemical compound CC(C)(C)CC(C)(C)C1=CC=CC=C1O XSXWOBXNYNULJG-UHFFFAOYSA-N 0.000 description 1
- RVBUZBPJAGZHSQ-UHFFFAOYSA-N 2-chlorobutanoic acid Chemical compound CCC(Cl)C(O)=O RVBUZBPJAGZHSQ-UHFFFAOYSA-N 0.000 description 1
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 1
- XYJLPCAKKYOLGU-UHFFFAOYSA-N 2-phosphonoethylphosphonic acid Chemical class OP(O)(=O)CCP(O)(O)=O XYJLPCAKKYOLGU-UHFFFAOYSA-N 0.000 description 1
- CVICEEPAFUYBJG-UHFFFAOYSA-N 5-chloro-2,2-difluoro-1,3-benzodioxole Chemical group C1=C(Cl)C=C2OC(F)(F)OC2=C1 CVICEEPAFUYBJG-UHFFFAOYSA-N 0.000 description 1
- ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 description 1
- 229910000013 Ammonium bicarbonate Inorganic materials 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical class OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical class NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 1
- 235000013162 Cocos nucifera Nutrition 0.000 description 1
- 244000060011 Cocos nucifera Species 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- PDQAZBWRQCGBEV-UHFFFAOYSA-N Ethylenethiourea Chemical compound S=C1NCCN1 PDQAZBWRQCGBEV-UHFFFAOYSA-N 0.000 description 1
- DBVJJBKOTRCVKF-UHFFFAOYSA-N Etidronic acid Chemical class OP(=O)(O)C(O)(C)P(O)(O)=O DBVJJBKOTRCVKF-UHFFFAOYSA-N 0.000 description 1
- IMQLKJBTEOYOSI-GPIVLXJGSA-N Inositol-hexakisphosphate Chemical class 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
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 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
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 229920000388 Polyphosphate Polymers 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-N Propionic acid Chemical class CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 1
- FENRSEGZMITUEF-ATTCVCFYSA-E [Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].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-] Chemical class [Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].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-] FENRSEGZMITUEF-ATTCVCFYSA-E 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 229910000288 alkali metal carbonate Inorganic materials 0.000 description 1
- 150000008041 alkali metal carbonates Chemical class 0.000 description 1
- 229910001508 alkali metal halide Inorganic materials 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- 235000012538 ammonium bicarbonate Nutrition 0.000 description 1
- 239000001099 ammonium carbonate Substances 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 235000003704 aspartic acid Nutrition 0.000 description 1
- 239000002585 base Substances 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
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000007844 bleaching agent Substances 0.000 description 1
- 229910021538 borax Inorganic materials 0.000 description 1
- 150000001642 boronic acid derivatives Chemical class 0.000 description 1
- YOPDMGNERLFFAW-UHFFFAOYSA-N bromo butanoate Chemical class CCCC(=O)OBr YOPDMGNERLFFAW-UHFFFAOYSA-N 0.000 description 1
- 239000000872 buffer Substances 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 229920003090 carboxymethyl hydroxyethyl cellulose Polymers 0.000 description 1
- 238000012512 characterization method Methods 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 235000011180 diphosphates Nutrition 0.000 description 1
- UQGFMSUEHSUPRD-UHFFFAOYSA-N disodium;3,7-dioxido-2,4,6,8,9-pentaoxa-1,3,5,7-tetraborabicyclo[3.3.1]nonane Chemical compound [Na+].[Na+].O1B([O-])OB2OB([O-])OB1O2 UQGFMSUEHSUPRD-UHFFFAOYSA-N 0.000 description 1
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
- 229940069096 dodecene Drugs 0.000 description 1
- GVGUFUZHNYFZLC-UHFFFAOYSA-N dodecyl benzenesulfonate;sodium Chemical compound [Na].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVGUFUZHNYFZLC-UHFFFAOYSA-N 0.000 description 1
- RIXFPXRYYYJJKF-UHFFFAOYSA-N dodecyl(dimethyl)phosphane Chemical compound CCCCCCCCCCCCP(C)C RIXFPXRYYYJJKF-UHFFFAOYSA-N 0.000 description 1
- JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecylamine Chemical compound CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 0.000 description 1
- SYELZBGXAIXKHU-UHFFFAOYSA-N dodecyldimethylamine N-oxide Chemical compound CCCCCCCCCCCC[N+](C)(C)[O-] SYELZBGXAIXKHU-UHFFFAOYSA-N 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 229940083124 ganglion-blocking antiadrenergic secondary and tertiary amines Drugs 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical class CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- 229920003063 hydroxymethyl cellulose Polymers 0.000 description 1
- 229940031574 hydroxymethyl cellulose Drugs 0.000 description 1
- SUMDYPCJJOFFON-UHFFFAOYSA-N isethionic acid Chemical class OCCS(O)(=O)=O SUMDYPCJJOFFON-UHFFFAOYSA-N 0.000 description 1
- IZWSFJTYBVKZNK-UHFFFAOYSA-N lauryl sulfobetaine Chemical compound CCCCCCCCCCCC[N+](C)(C)CCCS([O-])(=O)=O IZWSFJTYBVKZNK-UHFFFAOYSA-N 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- ZZUYIRISBMWFMV-UHFFFAOYSA-N methyl 4-chlorobutanoate Chemical compound COC(=O)CCCCl ZZUYIRISBMWFMV-UHFFFAOYSA-N 0.000 description 1
- 125000000325 methylidene group Chemical class [H]C([H])=* 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical group CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 1
- LTUGGBOPBQPPGK-UHFFFAOYSA-A octadecasodium;hexaphosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O LTUGGBOPBQPPGK-UHFFFAOYSA-A 0.000 description 1
- 239000003605 opacifier Substances 0.000 description 1
- MPQXHAGKBWFSNV-UHFFFAOYSA-N oxidophosphanium Chemical class [PH3]=O MPQXHAGKBWFSNV-UHFFFAOYSA-N 0.000 description 1
- HJZKOAYDRQLPME-UHFFFAOYSA-N oxidronic acid Chemical compound OP(=O)(O)C(O)P(O)(O)=O HJZKOAYDRQLPME-UHFFFAOYSA-N 0.000 description 1
- 229960004230 oxidronic acid Drugs 0.000 description 1
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- TWWBIMNLBUYJKB-UHFFFAOYSA-N phosphanyl acetate Chemical class CC(=O)OP TWWBIMNLBUYJKB-UHFFFAOYSA-N 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 150000003003 phosphines Chemical class 0.000 description 1
- UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 description 1
- XYFCBTPGUUZFHI-UHFFFAOYSA-O phosphonium Chemical compound [PH4+] XYFCBTPGUUZFHI-UHFFFAOYSA-O 0.000 description 1
- XYORSKKUGAGNPC-UHFFFAOYSA-N phosphonocarbonylphosphonic acid Chemical compound OP(O)(=O)C(=O)P(O)(O)=O XYORSKKUGAGNPC-UHFFFAOYSA-N 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 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
- 229920005646 polycarboxylate Polymers 0.000 description 1
- 239000001205 polyphosphate Substances 0.000 description 1
- 235000011176 polyphosphates Nutrition 0.000 description 1
- 229910000028 potassium bicarbonate Inorganic materials 0.000 description 1
- 235000015497 potassium bicarbonate Nutrition 0.000 description 1
- 239000011736 potassium bicarbonate Substances 0.000 description 1
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- KCXFHTAICRTXLI-UHFFFAOYSA-N propane-1-sulfonic acid Chemical compound CCCS(O)(=O)=O KCXFHTAICRTXLI-UHFFFAOYSA-N 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- UIIMBOGNXHQVGW-UHFFFAOYSA-M sodium bicarbonate Substances [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M sodium chloride Inorganic materials [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- FQENQNTWSFEDLI-UHFFFAOYSA-J sodium diphosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])([O-])=O FQENQNTWSFEDLI-UHFFFAOYSA-J 0.000 description 1
- 229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 1
- 229940045998 sodium isethionate Drugs 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
- DZCAZXAJPZCSCU-UHFFFAOYSA-K sodium nitrilotriacetate Chemical compound [Na+].[Na+].[Na+].[O-]C(=O)CN(CC([O-])=O)CC([O-])=O DZCAZXAJPZCSCU-UHFFFAOYSA-K 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 229940083982 sodium phytate Drugs 0.000 description 1
- 229940048086 sodium pyrophosphate Drugs 0.000 description 1
- 229910000031 sodium sesquicarbonate Inorganic materials 0.000 description 1
- 235000018341 sodium sesquicarbonate Nutrition 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- 239000004328 sodium tetraborate Substances 0.000 description 1
- LADXKQRVAFSPTR-UHFFFAOYSA-M sodium;2-hydroxyethanesulfonate Chemical compound [Na+].OCCS([O-])(=O)=O LADXKQRVAFSPTR-UHFFFAOYSA-M 0.000 description 1
- IWMMSZLFZZPTJY-UHFFFAOYSA-M sodium;3-(dodecylamino)propane-1-sulfonate Chemical compound [Na+].CCCCCCCCCCCCNCCCS([O-])(=O)=O IWMMSZLFZZPTJY-UHFFFAOYSA-M 0.000 description 1
- HWCHICTXVOMIIF-UHFFFAOYSA-M sodium;3-(dodecylamino)propanoate Chemical compound [Na+].CCCCCCCCCCCCNCCC([O-])=O HWCHICTXVOMIIF-UHFFFAOYSA-M 0.000 description 1
- LHYPLJGBYPAQAK-UHFFFAOYSA-M sodium;pentanoate Chemical compound [Na+].CCCCC([O-])=O LHYPLJGBYPAQAK-UHFFFAOYSA-M 0.000 description 1
- 238000005063 solubilization Methods 0.000 description 1
- 230000007928 solubilization Effects 0.000 description 1
- 230000003381 solubilizing effect Effects 0.000 description 1
- 238000000638 solvent extraction Methods 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- DIORMHZUUKOISG-UHFFFAOYSA-N sulfoformic acid Chemical compound OC(=O)S(O)(=O)=O DIORMHZUUKOISG-UHFFFAOYSA-N 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000008399 tap water Substances 0.000 description 1
- 235000020679 tap water Nutrition 0.000 description 1
- 229940095068 tetradecene Drugs 0.000 description 1
- JZBRFIUYUGTUGG-UHFFFAOYSA-J tetrapotassium;2-[2-[bis(carboxylatomethyl)amino]ethyl-(carboxylatomethyl)amino]acetate Chemical compound [K+].[K+].[K+].[K+].[O-]C(=O)CN(CC([O-])=O)CCN(CC([O-])=O)CC([O-])=O JZBRFIUYUGTUGG-UHFFFAOYSA-J 0.000 description 1
- 235000019818 tetrasodium diphosphate Nutrition 0.000 description 1
- UEUXEKPTXMALOB-UHFFFAOYSA-J tetrasodium;2-[2-[bis(carboxylatomethyl)amino]ethyl-(carboxylatomethyl)amino]acetate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]C(=O)CN(CC([O-])=O)CCN(CC([O-])=O)CC([O-])=O UEUXEKPTXMALOB-UHFFFAOYSA-J 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- VQOXUMQBYILCKR-UHFFFAOYSA-N tridecaene Natural products CCCCCCCCCCCC=C VQOXUMQBYILCKR-UHFFFAOYSA-N 0.000 description 1
- UNXRWKVEANCORM-UHFFFAOYSA-I triphosphate(5-) Chemical compound [O-]P([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O UNXRWKVEANCORM-UHFFFAOYSA-I 0.000 description 1
- 229910000406 trisodium phosphate Inorganic materials 0.000 description 1
- 235000019801 trisodium phosphate Nutrition 0.000 description 1
- WCTAGTRAWPDFQO-UHFFFAOYSA-K trisodium;hydrogen carbonate;carbonate Chemical compound [Na+].[Na+].[Na+].OC([O-])=O.[O-]C([O-])=O WCTAGTRAWPDFQO-UHFFFAOYSA-K 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/88—Ampholytes; Electroneutral compounds
- C11D1/886—Ampholytes containing P
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/54—Quaternary phosphonium compounds
- C07F9/5407—Acyclic saturated phosphonium compounds
-
- 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
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S516/00—Colloid systems and wetting agents; subcombinations thereof; processes of
- Y10S516/01—Wetting, emulsifying, dispersing, or stabilizing agents
- Y10S516/06—Protein or carboxylic compound containing
Definitions
- R is C -C alkyl; R and R are each C -C alkyl or hydroxyalkyl; n ranges from 3 to 5.
- the phosphonio carboxylates are employed with a builder material selected from water-soluble inorganic alkaline builder salts, organic alkaline sequestrant builder salts and mixtures thereof, in a ratio of detergent compound to builder material of from about 4:1 to about 1:20.
- a cool water laundering process is also disclosed.
- cool water as used in describing this invention is intended to mean aqueous washing solutions having a temperature within a range of from about 40 F. to about 95 F. This temperature characterization more generally is intended to mean temperatures substantially below those which are commonly associated with the usual household parlance of hot water.
- R is an alkyl group containing from 10 to 18 carbon atoms; R and R are each alkyl or hydroxy alkyl groups containing from 1 to 4 carbon atoms; 11 is 3, 4 or 5.
- the detergent compositions of this invention contain a phosphonio carboxylate of this class and a water soluble inorganic alkaline builder salt, an organic alkaline sequestrant builder salt or mixtures thereof, the ratio of weight of the detergent to the builder salt being in the range of from about 4:1 to 1:20.
- the phosphonio carboxylate compounds to which the present invention pertains can be prepared by reacting a suitable tertiary phosphine with an w-chloro (or wbromo) carboxylate and then saponifying the resulting ester.
- Equations (unbalanced) illustrating this synthesis are shown below; in the equations R R R and n have the same definitions as noted above and X is chloro or bromo:
- the base (MOH) can be NaOH or KOH.
- the solvent can be a lower monohydric alcohol such as isopropanol in which the alkali metal halide (MX) is insoluble.
- the temperature of the first reaction can range from 50 to 120 C.
- the time sufficient to achieve complete reaction is about 5 days when X above is chloro.
- the temperature of the saponification can range from 25 to C.
- the usual by-product is a sodium or potassium chloride or bromide.
- Phosphonio acetates and propionates can be prepared, but it has been found that such compounds are unstable and therefore unsuitable as detergents.
- EXAMPLE I 14.6 grams (0.017 mole) of methyl 4-chlorobutyrate (Cl(CH CO CH and 50 ml. of methanol were placed in a 500 ml. flask equipped with a condenser, thermometer and a stopper. These two ingredients were mixed with a mechanical stirrer and were maintained under argon gas under positive pressure.
- phosphonio carboxylates of the class of compounds of this invention can be prepared in a similar fashion using appropriate reactants to form the particular compounds desired.
- 5-chloro (or bromo) pentanoate or 6-chloro (or bromo) hexanoate ester can be employed to prepare phosphonio carboxylates wherein n in the general formula is 4 or 5.
- the starting phosphine material can likewise be selected to prepare the desired phosphonio carboxylate.
- the following phosphines can be employed with any of the w chloro or w bromo butyrates, pentanoates or hexanoates.
- the present invention also pertains to detergent compositions consisting essentially of a water soluble inorganic alkaline builder salt or a Water soluble organic alkaline sequestrant builder salt, or mixtures thereof, and a member of the class of phosphonio carboxylate detergent compounds having the general formula described above, which composition consists essentially of the detergent compound and a builder material in a ratio by Weight of detergent to builder of about 4:1 to about 1:20.
- the preferred ratio of the detergent to builder is 1:1 to about 1:10.
- the ratios and percentages referred to herein are all by weight unless otherwise noted.
- the built detergent compositions of this invention can be prepared as granular, tablet, or liquid compositions and perform effectively.
- granular and tablet compositions offering outstanding cool water washing performance can contain from 4% to 50% by weight of the phosphonio carboxylate detergent compound, the balance comprising essentially a selected builder material or mixtures of builders and any optional ingredients employed.
- Preferred granular and tablet compositions contain from about 15% to about 35% by weight of the phosphonio carboxylate detergent with the balance comprising the essential builder materials and other ingredients.
- built liquid detergents prepared according to the present invention have a slightly modified composition to compensate for the requirement of a liquid vehicle.
- Such liquid compositions can contain from about 2% to 25% by weight of the phosphonio carboxylate detergent, preferably from about 8% to about 18%, with the remainder comprised essentially of builder ingredients, and, of course, a liquid vehicle as described below.
- the ratio set forth above between the detergent and builder applies equally to all physical forms of the composition.
- Water soluble inorganic alkaline builder salts which can be used in this invention alone or in admixture are alkali metal carbonates, borates, phosphates, polyphosphates, bicarbonates and silicates. Ammonium or substituted ammonium, e.g., triethanol ammonium, salts of these materials can also be used. Specific examples of suitable salts are sodium tripolyphosphate, sodium carbonate, sodium tetraborate, sodium and potassium pyrophosphate, sodium and ammonium bicarbonate, potassium tripolyphosphate, sodium hexaphosphate, sodium sesquicarbonate, sodium orthophosphate and potassium bicarbonate.
- the preferred inorganic alkaline builders according to this invention are alkali metal tripolyphosphates for built granular and tablet compositions and alkail metal pyrophosphates for built liquid compositions. Potassium is the preferred alkali metal used in liquid compositions and sodium finds best application for granular or tablet compositions.
- organic alkaline sequestrant builder salts used in this invention alone or in admixture are alkali metal, ammonium or substituted ammonium, aminocarboxylates, e.g., sodium and potassium ethylenediaminetetraacetate, sodium and potassium N-(2-hydroxyethyl)-ethylenediaminetriacetates, sodium and potassium 'nitrilotriacetates and sodium, potassium and triethanolammonium N-(2-hydroxyethyl)-nitrilodiacetates.
- alkali metal salts of phytic acid e.g., sodium phytate are also suitable as organic alkaline sequestrant builder salts (see US. Pat. 2,739,942).
- Polyphosphonates are also valuable builders in terms of the present invention including specifically sodium and potassium salts of ethane 1 hydroxy-1,1-diphosphonic acid, sodium and potassium salts of methylene disphosphonic acid, sodium and potassium salts of ethylene diphosphonic acid, and sodium and potassium salts of ethane-1,1,2-triphosphonic acid.
- the phosphonio carboxylate compounds of this invention in combination with other cleaning agents such as anionic, nonionic, ampholytic and other zwitterionic organic detergent compounds.
- other cleaning agents such as anionic, nonionic, ampholytic and other zwitterionic organic detergent compounds.
- anionic detergents because of the sudsing characteristics of the latter.
- the ratio of the phosphonio car boxylate to such other detergent compound is about 10:1 to 1:5.
- the ratio of such a mixture to the builder salt should be within the previously prescribed range of 4:1 to 1:20.
- a composition prepared along these lines can contain from 4% to 50% of such a mixture and 5% to of a builder salt selected from water soluble inorganic alkaline builder salts, Water soluble organic sequestrant builder salts, and mixtures thereof, within the prescribed ratio range.
- anionic soap detergents which can be used in admixture with the carboxylate detergent, if desired, are the sodium, potassium, ammonium and alkylolammonium salts of higher detergent range fatty acids (C -C Particularly useful are the sodium and potassium salts of the mixtures of fatty acids derived from coconut oil and tallow, i.e., sodium or potassium tallow and coconut soap.
- Suitable anionic organic non-soap detergents in the form of their water soluble salts are: alkylglycerylethersulfonates; alkyl sulfates; alkyl monoglyceride sulfates or sulfonates; alkylpolyethenoxy ether sulfates; acylsarcosinates; acyl esters of isethionates; N-acyl N methyl taurides, alkyl-benzenesulfonates wherein the alkyl substituent is straight chain or branched chain; sulfonated on olefins; alkylphenol polyethenoxy sulfonates.
- alkyl and acyl groups contain 10 to 20 carbon atoms. They are used in the form of water soluble salts, the sodium, potassium, ammonium, and alkylolammonium salts, for example.'Specific'examples are: sodium lauryl sulfate, sodium tallow alkyl sulfate; sodium salt of sulfonated a tridecene; potassium N-methyl-N-lauroyl tauride; triethanolammonium tetrapropylbenzene sulfonate; sodium (linear) dodecyl benzene sulfonate.
- nonionic organic detergents which can be used in the compositions of this invention, if desired, are: polyethylene oxide condensates of alkylphenols wherein the alkyl group contains from 8 to 15 carbon atoms (e.g., t-octylphenol) and the ethylene oxide is present in a molar ratio of ethylene oxide to alkylphenol in the range of 8:1 to 20:1; condensation products of ethylene oxide with the product resulting from the reaction of propylene oxide and ethylene diamine wherein the molecular weight of the condensation products ranges from 5000 to 11,000; the condensation products of from about to 30 moles of ethylene oxide with one mole of a straight or branched chain aliphatic alcohol containing from 8 to 18 carbon atoms, e.g., condensation product of 6 moles of ethylene oxide with one mole of lauryl alcohol; higher alkyl di-lower alkyl amine or phosphine oxides, e.g., dodecyldimethyl
- Ampholytic synthetic detergents can be broadly described as derivatives of aliphatic secondary and tertiary amines in which the aliphatic radical can be straight chain or branched and wherein one of the aliphatic substituents contains from about 8 to about 18 carbon atoms and one contains an anionic water solubilizing group, e.g., carboxy, sulfonate, sulfate, phosphate, or phosphonate.
- an anionic water solubilizing group e.g., carboxy, sulfonate, sulfate, phosphate, or phosphonate.
- Examples of compounds falling within this definition are sodium 3-dodecylaminopropionate, 3(N methyl N hexadecyl amine) 2-hydroxy propane-l-sulfonate and its dodecyl homolog, sodium 3-dodecylaminopropane sulfonate, dodecyl-beta-alamine, N-alkyltaurines such as the one prepared reacting the dodecylamine with sodium isethionate according to the teaching of United States Pat. No. 2,658,072, N-higher alkyl aspartic acids such as those produced according to the teaching of United States Pat. No. 2,43 8,091, and the products sold under the trade name Miranol and described in United States Pat. No. 2,528,378.
- Zwitterionic synthetic detergents can be broadly described as derivatives of aliphatic quaternary ammonium, phosphonium and ternary sulfonium compounds, in which the aliphatic radical may be straight chain or branched, and wherein one of the aliphatic substituents contains from 10 to 18 carbon atoms and one contains an anionic water solubilization group, e.g., carboxy, sulfo, or sulfato.
- Examples of compounds falling within this definition are: 3-(N,N-dimethyl-N-hexadccylammonio)-2-hydroxypropane-l-sulfonate and the corresponding dodecyl and tetradecyl homologs and 3-(N,N-dimethyl-N-dodecylammonio)-propane-l-sulfonate and the corresponding hexadecyl and tetradecyl homologs.
- compositions containing members of the class of compounds described in this invention show exceptional cool water detergency was unpredictable in view of the fact that there is, as yet, virtually no generally accepted theory or background information on the mechanics of cool water detergency.
- cleaning agents such as sodium tallow alcohol sulfate or sodium dodecylbenzenesulfonate for example, which are good hot water (130-140 F.) detergent compounds exhibit a minimum of cleaning activity in cool water.
- the phosphonio carboxylate compounds of the present invention should be, comparatively speaking, as poor as any other conventional detergent compounds when used in cool water; certainly there is no reason to expect that they would behave otherwise.
- compositions containing the phosphonio carboxylate compounds of this invention are more effective in cool water than some of the commonly used commercially available detergent compositions are in hot water. It can, therefore, be seen that the structure of a given detergent compound which is effective in hot water has little or no discernible relation to the effectiveness of such compounds in cool water.
- the desired pH of the solution can be obtained by incorporating into the compositions of this invention a normal amount of a strongly alkaline material such as sodium silicate, i.e., up to about 10% by weight.
- a strongly alkaline material such as sodium silicate, i.e., up to about 10% by weight.
- the silicate acts as a buffer and also as a corrosion inhibitor.
- a laundering method incorporating the discovery of the present invention can be practiced in a number of different ways.
- the washing step is followed by rinsing and drying the fabrics.
- the washing solution can be prepared by adding the granular, tablet or liquid detergent composition prepared according to this invention to any container which contains cool water at a temperature ranging from about 40 F. to about 95 F., usually about F.
- the detergent composition concentration in solution can range from about .05% to .50% by total weight in the usual washing operation and should be added in sufricient amount to provide a concentration of at least 0.005% of the phosphonio carboxylate detergent compound.
- the fabrics can be added to the container or washer before or after the washing solution is added.
- an automatic agitator type washer generally employs a washing cycle which ranges from 8 to 15 imnutes.
- higher composition concentrations can be employed including solutions or pastes of up to 5%, 25% or even 50% and higher.
- the washing liquor is drained off or the fabrics are separated from the liquor and thereafter the fabrics are rinsed in clean water.
- the fabrics can be rinsed as many times as desired in order to insure that washing liquor is removed.
- Using an automatic washer it has been found that one or more spray rinses and one deep rinse are usually suflicient for this purpose.
- the bulk of the rinse water is usually drawn from or spun out of the fabrics.
- the fabrics are dried. Although rinsing and drying are usual and desirable steps, the important advantage of the invention is achieved in the washing step.
- Naturally soiled fabric swatches were washed for ten minutes in an aqueous solution of a detergent composition having a pH of 10 and containing 7 grains equivalent CaCO hardness per gallon.
- Detergent compositions were prepared containing only basic essentials, i.e., a detergent compound and a builder compound.
- the detergent compounds were respectively (1) a representative phosphonio carboxylate and (2) sodium tetrapropylenebenzene sulfonate (ABS); the builder compound in each composition was sodium tripolyphosphate.
- the phosphonio carboxylate compound was 4-(P,P-dimethyl, P-dodecyl phosphonio) butyrate (DMDPB).
- the phosphonio carboxylate detergent compound gave results in these tests, in water at 80 F. which were superior to the results obtained with a formula wherein sodium tetrapropylenebenzenesulfonate (ABS) was used as a cleaning agent in a washing solution having a temperature of 140 F.
- ABS sodium tetrapropylenebenzenesulfonate
- Sodium tetrapropylenebenzenesulfonate is widely regarded as a standard for comparison.
- Compositions which perform as good as or better than ABS at 140 F. generally can find application and commercial acceptance as detergent formulations. In situations such as the present invention where superior cleaning is obtained with different compounds at low temperatures, i.e., 80 F., the results are even more remarkable.
- compositions of this invention are outstandingly effective in water at a temperature ranging from 40 F. to 95 F.
- the preferred temperature range is about 60 F. to 90 F. Below about 60 F. it has been found that the granular detergent compositions of this invention are somewhat slower to dissolve, consequently it is preferred to use liquid compositions at such lower temperatures.
- compositions further illustrate the manner in which the invention can be practiced; they provide improved cool water detergency characteristics similar to that demonstrated in the soil removal comparison set forth above.
- the pHs of each of the compositions in aqueous solutions ranged from 9.5 to 11.5 at concentrations of about 0.25%. Included are both liquid and granular formulations. Mixtures of the phosphonio carboxylates and other detergents can be used. The examples are not to be construed as limiting the scope of the invention claimed hereinafter.
- These compositions are useful in automatic washers and conventional type washers employing cool water, 40 F. to F., as well as hand Washing operations:
- compositions of this invention Materials which are considered normal and desirable additives in liquid or granule detergent compositions can be added to the compositions of this invention without adversely affecting or modifying basic cleaning characteristics.
- a tarnish inhibitor such as benzotriazole or ethylene thiourea may be added in amounts up to about 1%.
- Fluorescers, perfume, bleaching agents, color, antiredeposition agents, antibacterial agents, thickening agents, opacifiers, and blending or viscosity control agents, while not essential in the compositions of this invention, may also be added.
- compositions described herein can also be used in conjunction with warm and hot Water.
- a detergent composition having superior cleaning ability in aqueous solutions having a temperature within a range of from about 40 F. to about 95 F. consisting essentially of (1) a phosphonio carboxylate detergent compound of the general formula:
- R is an alkyl group containing from 10 to 18 carbon atoms; R and R are each alkyl or hydroxy alkyl groups containing from 1 to 4 carbon atoms; wherein n ranges from 3 to 5; and (2) a builder material selected from the group consisting of water-soluble inorganic alkaline builder salts, organic alkaline sequestrant builder salts, and mixtures thereof, the ratio by weight of said detergent compound to said builder material being in the range of about 4:1 to about 1:20.
- the detergent composition of claim 1 wherein the ratio of said detergent compound to said builder is from 1:1 to about 1:10, by weight and the phosphonio car boxylate compound is 4(P,P-dimethyl, P-dodecyl phosphonio) butyrate.
- a laundering process comprising the steps of immersing soiled fabrics and garments into an aqueous solution having a temperature within the range of from about 40 to about 95 F., and a pH of from about 8 to about 12, said aqueous solution containing at least about .05 by weight of the detergent composition of claim 1.
- a built detergent composition consisting essentially of 4% to 50% of a mixture of a phosphonio carboxylate detergent compound of the formula groups containing from 1 to 4 carbon atoms; wherein n ranges from 3 to 5; and an organic anionic detergent, the ratio of the compound to said organic detergent being in the range of 10:1 to 1:5 and from 5% to of a builder material selected from the group consisting of water-soluble inorganic alkaline builder salts, watersoluble organic alkaline sequestrant builder salts, and mixtures thereof.
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Abstract
PHOSPHONIO CARBOXYLATES HAVING EFFECTIVE DETERGENCY IN COOL WATER LAUNDERING AND HAVING THE FOLLOWING GENERAL FORMULA ARE DISCLOSED:
R1-P(+)(-R2)(-R3)-(CH2)N-COO(-)
R1 IS C10-C18 ALKYL; R2 AND R3 ARE EACH C1-C4 ALKYL OR HYDROXYALKYL; N RANGES FROM 3 TO 5. THE PHOSPHONIO CARBOXYLATES ARE EMPLOYED WITH A BUILDER MATERIAL SELECTED FROM WATER-SOLUBLE INORGANIC ALKALINE BUILDER SALTS, ORGANIC ALKALINE SEQUESTRANT BUILDER SALTS AND MIXTURES THEREOF, IN A RATIO OF DETERGENT COMPOUND TO BUILDER MATERIAL OF FROM ABOUT 4:1 TO ABOUT 1:20. A COOL WATER LAUNDERING PROCESS IS ALSO DISCLOSED.
R1-P(+)(-R2)(-R3)-(CH2)N-COO(-)
R1 IS C10-C18 ALKYL; R2 AND R3 ARE EACH C1-C4 ALKYL OR HYDROXYALKYL; N RANGES FROM 3 TO 5. THE PHOSPHONIO CARBOXYLATES ARE EMPLOYED WITH A BUILDER MATERIAL SELECTED FROM WATER-SOLUBLE INORGANIC ALKALINE BUILDER SALTS, ORGANIC ALKALINE SEQUESTRANT BUILDER SALTS AND MIXTURES THEREOF, IN A RATIO OF DETERGENT COMPOUND TO BUILDER MATERIAL OF FROM ABOUT 4:1 TO ABOUT 1:20. A COOL WATER LAUNDERING PROCESS IS ALSO DISCLOSED.
Description
United States US. Cl. 252135 7 Claims ABSTRACT OF THE DISCLOSURE Phosphonio carboxylates having effective detergency in cool water laundering and having the following general formula are disclosed:
R is C -C alkyl; R and R are each C -C alkyl or hydroxyalkyl; n ranges from 3 to 5. The phosphonio carboxylates are employed with a builder material selected from water-soluble inorganic alkaline builder salts, organic alkaline sequestrant builder salts and mixtures thereof, in a ratio of detergent compound to builder material of from about 4:1 to about 1:20. A cool water laundering process is also disclosed.
CROSS-REFERENCE TO RELATED APPLICATION This application is a division of US. patent application Ser. No. 574,470, filed Aug. 23, 1966, now U.S. Pat. 3,504,024 entitled Phosphonio Carboxylates and Detergent Compositions Containing Same, in the name of Francis L. Diehl et al.
This invention relates to phosphonio carboxylates and detergent compositions containing same which are especially effective in cool water. The term cool water as used in describing this invention is intended to mean aqueous washing solutions having a temperature within a range of from about 40 F. to about 95 F. This temperature characterization more generally is intended to mean temperatures substantially below those which are commonly associated with the usual household parlance of hot water.
Some garments or fabrics cannot be washed in hot water, i.e., say in excess of about 110 F., without running the risk of damaging the material by shrinkage or altering the handle or feel of the fabric or by adversely affecting dyes or by increasing wrinkling in washand-wear or minimum care garments. For such laundering situations fabric and material manufacturers recommend the use of cool water. Conventional detergents, however, are known to be less eifective as cleaning agents, i.e., removing soil, in cool aqueous solutions. There is no question that the presently available detergent compositions can be used under such circumstances but with varying degrees of successful cleaning results. To compensate for the poorer cleaning performance, consumers are generally inclined to use excessive amounts of the detergent compositions. Such economic waste is unfortunate but has been necessary prior to the present invention due to the lack of detergent compositions which are specially formulated to be effective cleaning agents in cool water.
It is an object of this invention to provide novel detergent compounds and detergent compositions containing same which are especially effective in cleaning soiled atent O fabrics in cool aqueous washing solutions and a method for using such a composition in laundering with cool water.
Other objects will be readily apparent to those skilled in the art from a review of the following detailed description of the present invention.
This object of the present invention is achieved with novel phosphonio carboxylate detergent compounds having the general formula noted below and built detergent compositions containing same:
R is an alkyl group containing from 10 to 18 carbon atoms; R and R are each alkyl or hydroxy alkyl groups containing from 1 to 4 carbon atoms; 11 is 3, 4 or 5. The detergent compositions of this invention contain a phosphonio carboxylate of this class and a water soluble inorganic alkaline builder salt, an organic alkaline sequestrant builder salt or mixtures thereof, the ratio of weight of the detergent to the builder salt being in the range of from about 4:1 to 1:20.
It has been surprisingly discovered that certain phosphonio carboxylate compounds having the formula set forth above possess unusually eifective cleaning power in aqueous solutions having the cool temperatures defined above. These unexpected cleaning properties of the zwitterionic compounds of this invention are demonstreated by the experimental data presented below. Of the phosphonio carboxylate detergent compounds described herein, best cool water cleaning results are obtained when R is dodecyl, R and R are each methyl and n is 3, i.e., 4- (P,P dimethyl-P-dodecyl phosphonio)butyrate.
The phosphonio carboxylate compounds to which the present invention pertains can be prepared by reacting a suitable tertiary phosphine with an w-chloro (or wbromo) carboxylate and then saponifying the resulting ester.
Equations (unbalanced) illustrating this synthesis are shown below; in the equations R R R and n have the same definitions as noted above and X is chloro or bromo:
The base (MOH) can be NaOH or KOH. The solvent can be a lower monohydric alcohol such as isopropanol in which the alkali metal halide (MX) is insoluble. The temperature of the first reaction can range from 50 to 120 C. The time sufficient to achieve complete reaction is about 5 days when X above is chloro. The temperature of the saponification can range from 25 to C. The usual by-product is a sodium or potassium chloride or bromide.
Phosphonio acetates and propionates can be prepared, but it has been found that such compounds are unstable and therefore unsuitable as detergents.
The following example illustrates the preparation of the compounds of this invention.
EXAMPLE I 14.6 grams (0.017 mole) of methyl 4-chlorobutyrate (Cl(CH CO CH and 50 ml. of methanol were placed in a 500 ml. flask equipped with a condenser, thermometer and a stopper. These two ingredients were mixed with a mechanical stirrer and were maintained under argon gas under positive pressure.
22.4 grams (0.0974 mole) of dimethyldodecylphosphine were added from a syringe under the surface of the mixture of 'y chlorobutyrate and methanol. The resulting reaction mixture was heated to refiux temperature; refluxing continued for days. The mixture was then cooled to 20 C. with tap water and the methanol evaporated in vacuo. The resulting ester was saponified with 7.06 grams of 85% aqueous KOH (0.107 mole) in 250 ml. of isopropanol, maintaining the temperature below 30 C. The reaction mixture was permitted to stand for 3% hours. The KCl in the saponified mixture precipitated from the isopropanol in crystalline form, was filtered off and the solvent evaporated to leave 4-(P,P dimethyl-P-dodecyl phosphonio) butyrate.
Other phosphonio carboxylates of the class of compounds of this invention can be prepared in a similar fashion using appropriate reactants to form the particular compounds desired. For example, 5-chloro (or bromo) pentanoate or 6-chloro (or bromo) hexanoate ester can be employed to prepare phosphonio carboxylates wherein n in the general formula is 4 or 5. The starting phosphine material can likewise be selected to prepare the desired phosphonio carboxylate. For example, the following phosphines can be employed with any of the w chloro or w bromo butyrates, pentanoates or hexanoates.
diethyltetradecylphosphine bis( l-hydroxymethyl)hexadecyl phosphine dipropyldecylphosphine dimethyloctadecylphosphine hydroxyethyl methyl dodecyl phosphine While the class of phosphonio carboxylate compounds just described can be employed alone as cool water detergent compounds on easily cleanable materials, more outstanding performances are obtained when they are mixed with other ingredients which enhance or build the cleaning power of detergent compounds, i.e., so-called builders or detergency-enhancing compounds. Such built or heavy-duty detergency is essential with hard-to-clean fabrics such as cotton. According to the present invention, therefore, the phosphonio carboxylate detergent compounds are preferably used in conjunction with such other ingredients which substantially improve cleaning power. While the term builder is used herein in its singular form, the term is intended to cover mixtures of such compounds also.
The present invention also pertains to detergent compositions consisting essentially of a water soluble inorganic alkaline builder salt or a Water soluble organic alkaline sequestrant builder salt, or mixtures thereof, and a member of the class of phosphonio carboxylate detergent compounds having the general formula described above, which composition consists essentially of the detergent compound and a builder material in a ratio by Weight of detergent to builder of about 4:1 to about 1:20. The preferred ratio of the detergent to builder is 1:1 to about 1:10. The ratios and percentages referred to herein are all by weight unless otherwise noted.
The built detergent compositions of this invention can be prepared as granular, tablet, or liquid compositions and perform effectively. Within the above detergent to builder ratio range, granular and tablet compositions offering outstanding cool water washing performance can contain from 4% to 50% by weight of the phosphonio carboxylate detergent compound, the balance comprising essentially a selected builder material or mixtures of builders and any optional ingredients employed. Preferred granular and tablet compositions contain from about 15% to about 35% by weight of the phosphonio carboxylate detergent with the balance comprising the essential builder materials and other ingredients. On the other hand, built liquid detergents prepared according to the present invention have a slightly modified composition to compensate for the requirement of a liquid vehicle. Such liquid compositions can contain from about 2% to 25% by weight of the phosphonio carboxylate detergent, preferably from about 8% to about 18%, with the remainder comprised essentially of builder ingredients, and, of course, a liquid vehicle as described below. The ratio set forth above between the detergent and builder applies equally to all physical forms of the composition.
Water soluble inorganic alkaline builder salts which can be used in this invention alone or in admixture are alkali metal carbonates, borates, phosphates, polyphosphates, bicarbonates and silicates. Ammonium or substituted ammonium, e.g., triethanol ammonium, salts of these materials can also be used. Specific examples of suitable salts are sodium tripolyphosphate, sodium carbonate, sodium tetraborate, sodium and potassium pyrophosphate, sodium and ammonium bicarbonate, potassium tripolyphosphate, sodium hexaphosphate, sodium sesquicarbonate, sodium orthophosphate and potassium bicarbonate. The preferred inorganic alkaline builders according to this invention are alkali metal tripolyphosphates for built granular and tablet compositions and alkail metal pyrophosphates for built liquid compositions. Potassium is the preferred alkali metal used in liquid compositions and sodium finds best application for granular or tablet compositions.
Examples of suitable organic alkaline sequestrant builder salts used in this invention alone or in admixture are alkali metal, ammonium or substituted ammonium, aminocarboxylates, e.g., sodium and potassium ethylenediaminetetraacetate, sodium and potassium N-(2-hydroxyethyl)-ethylenediaminetriacetates, sodium and potassium 'nitrilotriacetates and sodium, potassium and triethanolammonium N-(2-hydroxyethyl)-nitrilodiacetates. Mixed salts of these polycarboxylates are also suitable. The alkali metal salts of phytic acid, e.g., sodium phytate are also suitable as organic alkaline sequestrant builder salts (see US. Pat. 2,739,942).
Polyphosphonates are also valuable builders in terms of the present invention including specifically sodium and potassium salts of ethane 1 hydroxy-1,1-diphosphonic acid, sodium and potassium salts of methylene disphosphonic acid, sodium and potassium salts of ethylene diphosphonic acid, and sodium and potassium salts of ethane-1,1,2-triphosphonic acid. Other examples include the alkali metal salts of ethane-2-carboxy-1,1-diphosphonic acid, hydroxymethanediphosphonic acid, carbonyldiphosphonic acid, ethane l hydroxy-1,1,2-triphosphonic acid, ethane 2 hydroxy-l,1,2-triphosphonic acid, propane 1,1,3,3 tetraphosphonic acid, propane-1,1,2,3- tetraphosphonic acid, and propane-1,2,2,3-tetraphosphonic acid.
Besides the builders being used in the form of mixtures it is also possible according to the present invention to use the phosphonio carboxylate compounds of this invention in combination with other cleaning agents such as anionic, nonionic, ampholytic and other zwitterionic organic detergent compounds. When it is desired to use such phosphonio carboxylate compounds in combination with other detergent compounds, they are preferably utilized with anionic detergents because of the sudsing characteristics of the latter. The ratio of the phosphonio car boxylate to such other detergent compound is about 10:1 to 1:5. If it is desired to use such a phosphonio carboxylate in admixture with another detergent compound as the active portion of a cleaning composition, the ratio of such a mixture to the builder salt should be within the previously prescribed range of 4:1 to 1:20. A composition prepared along these lines can contain from 4% to 50% of such a mixture and 5% to of a builder salt selected from water soluble inorganic alkaline builder salts, Water soluble organic sequestrant builder salts, and mixtures thereof, within the prescribed ratio range.
Examples of anionic soap detergents which can be used in admixture with the carboxylate detergent, if desired, are the sodium, potassium, ammonium and alkylolammonium salts of higher detergent range fatty acids (C -C Particularly useful are the sodium and potassium salts of the mixtures of fatty acids derived from coconut oil and tallow, i.e., sodium or potassium tallow and coconut soap. Examples of suitable anionic organic non-soap detergents in the form of their water soluble salts are: alkylglycerylethersulfonates; alkyl sulfates; alkyl monoglyceride sulfates or sulfonates; alkylpolyethenoxy ether sulfates; acylsarcosinates; acyl esters of isethionates; N-acyl N methyl taurides, alkyl-benzenesulfonates wherein the alkyl substituent is straight chain or branched chain; sulfonated on olefins; alkylphenol polyethenoxy sulfonates. In these compounds the alkyl and acyl groups, respectively, contain 10 to 20 carbon atoms. They are used in the form of water soluble salts, the sodium, potassium, ammonium, and alkylolammonium salts, for example.'Specific'examples are: sodium lauryl sulfate, sodium tallow alkyl sulfate; sodium salt of sulfonated a tridecene; potassium N-methyl-N-lauroyl tauride; triethanolammonium tetrapropylbenzene sulfonate; sodium (linear) dodecyl benzene sulfonate.
Examples of nonionic organic detergents which can be used in the compositions of this invention, if desired, are: polyethylene oxide condensates of alkylphenols wherein the alkyl group contains from 8 to 15 carbon atoms (e.g., t-octylphenol) and the ethylene oxide is present in a molar ratio of ethylene oxide to alkylphenol in the range of 8:1 to 20:1; condensation products of ethylene oxide with the product resulting from the reaction of propylene oxide and ethylene diamine wherein the molecular weight of the condensation products ranges from 5000 to 11,000; the condensation products of from about to 30 moles of ethylene oxide with one mole of a straight or branched chain aliphatic alcohol containing from 8 to 18 carbon atoms, e.g., condensation product of 6 moles of ethylene oxide with one mole of lauryl alcohol; higher alkyl di-lower alkyl amine or phosphine oxides, e.g., dodecyldimethylamine oxide or dodecyldimethyl phosphine oxide; alkyl methyl sulfoxides such as dodecyl methyl sulfoxide.
Ampholytic synthetic detergents can be broadly described as derivatives of aliphatic secondary and tertiary amines in which the aliphatic radical can be straight chain or branched and wherein one of the aliphatic substituents contains from about 8 to about 18 carbon atoms and one contains an anionic water solubilizing group, e.g., carboxy, sulfonate, sulfate, phosphate, or phosphonate. Examples of compounds falling within this definition are sodium 3-dodecylaminopropionate, 3(N methyl N hexadecyl amine) 2-hydroxy propane-l-sulfonate and its dodecyl homolog, sodium 3-dodecylaminopropane sulfonate, dodecyl-beta-alamine, N-alkyltaurines such as the one prepared reacting the dodecylamine with sodium isethionate according to the teaching of United States Pat. No. 2,658,072, N-higher alkyl aspartic acids such as those produced according to the teaching of United States Pat. No. 2,43 8,091, and the products sold under the trade name Miranol and described in United States Pat. No. 2,528,378.
Zwitterionic synthetic detergents can be broadly described as derivatives of aliphatic quaternary ammonium, phosphonium and ternary sulfonium compounds, in which the aliphatic radical may be straight chain or branched, and wherein one of the aliphatic substituents contains from 10 to 18 carbon atoms and one contains an anionic water solubilization group, e.g., carboxy, sulfo, or sulfato. Examples of compounds falling within this definition are: 3-(N,N-dimethyl-N-hexadccylammonio)-2-hydroxypropane-l-sulfonate and the corresponding dodecyl and tetradecyl homologs and 3-(N,N-dimethyl-N-dodecylammonio)-propane-l-sulfonate and the corresponding hexadecyl and tetradecyl homologs.
The discovery that the compositions containing members of the class of compounds described in this invention show exceptional cool water detergency was unpredictable in view of the fact that there is, as yet, virtually no generally accepted theory or background information on the mechanics of cool water detergency. Moreover, cleaning agents such as sodium tallow alcohol sulfate or sodium dodecylbenzenesulfonate for example, which are good hot water (130-140 F.) detergent compounds exhibit a minimum of cleaning activity in cool water. One would be led to assume that the phosphonio carboxylate compounds of the present invention should be, comparatively speaking, as poor as any other conventional detergent compounds when used in cool water; certainly there is no reason to expect that they would behave otherwise. As has been discovered, however, the compositions containing the phosphonio carboxylate compounds of this invention are more effective in cool water than some of the commonly used commercially available detergent compositions are in hot water. It can, therefore, be seen that the structure of a given detergent compound which is effective in hot water has little or no discernible relation to the effectiveness of such compounds in cool water.
It has also been found that maximum cleaning occurs with the compositions of this invention when the pH of the washing solution, at cool water temperatures as herein defined is within the range of from about 8 to about 12 with the preferred pH range being 9.5 to 11.5. Using normal amounts of water for washing, the desired pH of the solution can be obtained by incorporating into the compositions of this invention a normal amount of a strongly alkaline material such as sodium silicate, i.e., up to about 10% by weight. The silicate acts as a buffer and also as a corrosion inhibitor.
A laundering method incorporating the discovery of the present invention can be practiced in a number of different ways. Preferably the washing step is followed by rinsing and drying the fabrics. The washing solution can be prepared by adding the granular, tablet or liquid detergent composition prepared according to this invention to any container which contains cool water at a temperature ranging from about 40 F. to about 95 F., usually about F. The detergent composition concentration in solution can range from about .05% to .50% by total weight in the usual washing operation and should be added in sufricient amount to provide a concentration of at least 0.005% of the phosphonio carboxylate detergent compound. The fabrics can be added to the container or washer before or after the washing solution is added. As is usual in a washing step, the fabrics are then agitated in the detergent solution. While the period of time may vary, an automatic agitator type washer, generally employs a washing cycle which ranges from 8 to 15 imnutes. In special situations, such as hand washing in basins, pools or streams, higher composition concentrations can be employed including solutions or pastes of up to 5%, 25% or even 50% and higher.
After the washing step, the washing liquor is drained off or the fabrics are separated from the liquor and thereafter the fabrics are rinsed in clean water. The fabrics can be rinsed as many times as desired in order to insure that washing liquor is removed. Using an automatic washer, it has been found that one or more spray rinses and one deep rinse are usually suflicient for this purpose. Between and after rinsing steps, the bulk of the rinse water is usually drawn from or spun out of the fabrics. After rinsing, the fabrics are dried. Although rinsing and drying are usual and desirable steps, the important advantage of the invention is achieved in the washing step.
The surprisingly effective cool water performance characteristics of the phosphonio carboxylate compounds described herein are demonstrated by conducting the following tests.
Naturally soiled fabric swatches (desized cotton print cloth) were washed for ten minutes in an aqueous solution of a detergent composition having a pH of 10 and containing 7 grains equivalent CaCO hardness per gallon. Detergent compositions were prepared containing only basic essentials, i.e., a detergent compound and a builder compound. The detergent compounds were respectively (1) a representative phosphonio carboxylate and (2) sodium tetrapropylenebenzene sulfonate (ABS); the builder compound in each composition was sodium tripolyphosphate. The phosphonio carboxylate compound was 4-(P,P-dimethyl, P-dodecyl phosphonio) butyrate (DMDPB). By using the same builder compound in each composition, any variations in cleaning performance could be directly attributed to the specific detergent being evaluated. The concentration by weight in the washing solution of the detergent compound was .03%; the concentration of the builder was .06%.
These two compositions were compared in two separate comparisons for their soil removal properties, the phosphonio carboxylate in a washing solution at 80 F. and the ABS in a washing solution at 140 F. Soil removal, expressed as a percentage of the soil originally present on the soiled swatches, was determined. The amounts of soil present (a) on the cloth swatches after washing and drying and (b) on similar unwashed swatches were determined by solvent extraction.
The phosphonio carboxylate detergent compound gave results in these tests, in water at 80 F. which were superior to the results obtained with a formula wherein sodium tetrapropylenebenzenesulfonate (ABS) was used as a cleaning agent in a washing solution having a temperature of 140 F. Sodium tetrapropylenebenzenesulfonate is widely regarded as a standard for comparison. Compositions which perform as good as or better than ABS at 140 F. generally can find application and commercial acceptance as detergent formulations. In situations such as the present invention where superior cleaning is obtained with different compounds at low temperatures, i.e., 80 F., the results are even more remarkable.
The same superiority of the phosphonio carboxylate compound at 80 F. over ABS at 140 F. Was demonstrated in a similar washing test employing soiled mens White dress shirts where the collars and cuffs were used as the basis for comparing cleaning ability of compositions employing these two detergent compounds.
Substantially the same performance advantages are observed by the housewife when doing the home laundry in water ranging from 40 to 95 F., particularly laundering cotton goods. Woolens, synthetic fibers and washand-wear garments washed in the same manner are cleaned as efiiciently when washed according to the process of this invention and using the compositions of this invention as they would be if they were washed in conventional detergent compositions at hot water temperatures, yet a minimum of shrinkage and wrinkling takes place and the color and feel of the fabric is preserved to a greater extent.
While the compositions of this invention are outstandingly effective in water at a temperature ranging from 40 F. to 95 F. the preferred temperature range is about 60 F. to 90 F. Below about 60 F. it has been found that the granular detergent compositions of this invention are somewhat slower to dissolve, consequently it is preferred to use liquid compositions at such lower temperatures.
The following compositions further illustrate the manner in which the invention can be practiced; they provide improved cool water detergency characteristics similar to that demonstrated in the soil removal comparison set forth above. The pHs of each of the compositions in aqueous solutions ranged from 9.5 to 11.5 at concentrations of about 0.25%. Included are both liquid and granular formulations. Mixtures of the phosphonio carboxylates and other detergents can be used. The examples are not to be construed as limiting the scope of the invention claimed hereinafter. These compositions are useful in automatic washers and conventional type washers employing cool water, 40 F. to F., as well as hand Washing operations:
EXAMPLE II SolidGranules Percent 4-(P,P-diethyl, P-dodecyl phosphonio) butyrate 17.5
Sodium tripolyphosphate 50 Sodium silicate (Na O:SiO =1:2.5) 10.0 Sodiurm sulfate 17.5 Moisture 5.0
EXAMPLE III Compressed Granules-Ta'blet Percent 4-(P,P-dipropyl, P-tetradecyl phosphonio) butyrate 31 Tetra sodium pyrophosphate 52 Trisodium phosphate 10 Moisture 7 EXAMPLE IV SolidGranules Percent 5-(P,P bis(2 hydroxyethyl), P-hexadecyl phosphonio) pentanoate 32 Triso dium ethane- 1 -hydroxy- 1 1-2-triphosphonate 64 Moisture 4 EXAMPLE V SolidGranules Percent 3 (N,N dimethyl N hexadecyl ammonio) propane-l-sulfonate 20 6-(P,P,dipropyl, P-dodecyl phosphonio)-hexanoate 25 Sodium tripolyphosphate 35 Sodium carbonate 10 Sodium silicate (Na ozSiO' 1:25) 5 Moisture 5 EXAMPLE VI SolidGranules Percent 4 (P,P dimethyl, P hexadecyl phosphonio) butyrate 20 Sodium tallow alcohol sulfate 10 Trisodium ethane-l-hydroxy-l,l-diphosphonate 20 Sodium tripolyphosphate 10 Sodium nitrilotriacetate 10 Sodium sulfate 8 Sodium silicate (Na O:SiO =1:2.5) 11 Moisture 11 EXAMPLE VII Liquid Percent 4-(P,P-dimethyl, P-decyl phosphonio)butyrate 5.0 Sodium salt of S0 sulfonated 1:1 weight mixture of dodecene and a tetradecene 10.0 Tetrapotassium pyrophosphate 19.0 Sodium silicate (Na O:SiO =1:1.6) 3.8 Potassium toluene sulfonate 8.5 Carboxymethyl hydroxyethyl cellulose .3 Water Balanc 9 EXAMPLE VIII Liquid Percent (P,P bis(2 hydroxypropyl), P dodecyl phosphonio) pentanoate Sodium (linear) dodecyl benzene sulfonate 6.0 Tetrapotassium propane-1,1,3,3-tetraphosphonate 20.0 Sodium silicate (Na O:SiO =1:1.6) 3.8 Potassium toluene sulfonate 8.5 Carboxymethyl hydroxymethyl cellulose .3 Water Balance EXAMPLE IX Solid-Granules Percent 4-(P,P-dipropyl, P-dodecyl phosphonio)butyrate 5 Condensation product of moles of ethylene oxide and one mole of tallow fatty alcohol 5 Sodium (linear) tridecyl benzene sulfonate 10 Dodecyldimethyl phosphine oxide 5 Coconut oil soap 5 Sodium tripolyphosphate 50 Tetrasodium ethylene diamine tetraacetate It Will be appreciated that the phosphonio carboxylate compounds used in the present invention can be incorporated into many other liquid or granular detergent compositions with suitable adjustments being made in the other components.
Materials which are considered normal and desirable additives in liquid or granule detergent compositions can be added to the compositions of this invention without adversely affecting or modifying basic cleaning characteristics. For example, a tarnish inhibitor such as benzotriazole or ethylene thiourea may be added in amounts up to about 1%. Fluorescers, perfume, bleaching agents, color, antiredeposition agents, antibacterial agents, thickening agents, opacifiers, and blending or viscosity control agents, while not essential in the compositions of this invention, may also be added.
While the present invention finds exceptional application in cool water washing situations, the compositions described herein can also be used in conjunction with warm and hot Water.
What is claimed herein is:
1. A detergent composition having superior cleaning ability in aqueous solutions having a temperature within a range of from about 40 F. to about 95 F. consisting essentially of (1) a phosphonio carboxylate detergent compound of the general formula:
wherein R is an alkyl group containing from 10 to 18 carbon atoms; R and R are each alkyl or hydroxy alkyl groups containing from 1 to 4 carbon atoms; wherein n ranges from 3 to 5; and (2) a builder material selected from the group consisting of water-soluble inorganic alkaline builder salts, organic alkaline sequestrant builder salts, and mixtures thereof, the ratio by weight of said detergent compound to said builder material being in the range of about 4:1 to about 1:20.
2. The detergent composition of claim 1 wherein the ratio of said detergent compound to said builder is from 1:1 to about 1:10, by weight and the phosphonio car boxylate compound is 4(P,P-dimethyl, P-dodecyl phosphonio) butyrate.
3. The detergent composition of claim 1 in which the aqueous solution has a pH of from about 8 to about 12.
4. The detergent composition of claim 2 wherein the preferred pH range is between about 9.5 and 11.5.
5. The detergent composition of claim 4 wherein said builder material is sodium tripolyphosphate.
6. A laundering process comprising the steps of immersing soiled fabrics and garments into an aqueous solution having a temperature within the range of from about 40 to about 95 F., and a pH of from about 8 to about 12, said aqueous solution containing at least about .05 by weight of the detergent composition of claim 1.
7. A built detergent composition consisting essentially of 4% to 50% of a mixture of a phosphonio carboxylate detergent compound of the formula groups containing from 1 to 4 carbon atoms; wherein n ranges from 3 to 5; and an organic anionic detergent, the ratio of the compound to said organic detergent being in the range of 10:1 to 1:5 and from 5% to of a builder material selected from the group consisting of water-soluble inorganic alkaline builder salts, watersoluble organic alkaline sequestrant builder salts, and mixtures thereof.
References Cited UNITED STATES PATENTS 3,504,024 3/1970 Diehl et al 260526 3,400,148 9/1968 Quimby 260502.4 3,390,095 6/1968 Diehl 252l38 3,125,555 3/1964 Pare 260-526 LEON D. ROSDOL, Primary Examiner D. L. ALBRECHT, Assistant Examiner U.S. Cl. X.R.
Applications Claiming Priority (2)
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US57447066A | 1966-08-23 | 1966-08-23 | |
US590070A | 1970-01-26 | 1970-01-26 |
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US3560391A true US3560391A (en) | 1971-02-02 |
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US574470A Expired - Lifetime US3504024A (en) | 1966-08-23 | 1966-08-23 | Phosphonio carboxylates |
US5900*[A Expired - Lifetime US3560391A (en) | 1966-08-23 | 1970-01-26 | Detergent compositions containing phosphonio carboxylates |
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US574470A Expired - Lifetime US3504024A (en) | 1966-08-23 | 1966-08-23 | Phosphonio carboxylates |
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DE2540260C2 (en) * | 1975-09-10 | 1984-03-01 | Hoechst Ag, 6230 Frankfurt | Phosphor betaines and processes for their preparation |
DE2540232C2 (en) * | 1975-09-10 | 1983-12-08 | Hoechst Ag, 6230 Frankfurt | Phosphor betaines and processes for their preparation |
EP0004686A3 (en) * | 1978-03-31 | 1979-10-31 | THE PROCTER & GAMBLE COMPANY | Anti-ulcer composition |
US4259249A (en) * | 1979-06-13 | 1981-03-31 | The Procter & Gamble Company | Preparation of hydroxyl zwitterionic compounds |
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US3125555A (en) * | 1964-03-17 | Vinoxycarbonylmethyltrialkylphospho- |
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