US3585145A - Low sudsing detergent compositions - Google Patents
Low sudsing detergent compositions Download PDFInfo
- Publication number
- US3585145A US3585145A US746274A US3585145DA US3585145A US 3585145 A US3585145 A US 3585145A US 746274 A US746274 A US 746274A US 3585145D A US3585145D A US 3585145DA US 3585145 A US3585145 A US 3585145A
- Authority
- US
- United States
- Prior art keywords
- sodium
- suds
- detergent
- oxide
- water
- 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 95
- 239000003599 detergent Substances 0.000 title abstract description 58
- 239000003795 chemical substances by application Substances 0.000 abstract description 37
- 239000000344 soap Substances 0.000 abstract description 29
- 239000000271 synthetic detergent Substances 0.000 abstract description 23
- -1 alkyl radical Chemical class 0.000 description 42
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 36
- 150000001875 compounds Chemical class 0.000 description 31
- 125000004432 carbon atom Chemical group C* 0.000 description 26
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 21
- 125000003709 fluoroalkyl group Chemical group 0.000 description 18
- 239000011734 sodium Substances 0.000 description 17
- 229910052708 sodium Inorganic materials 0.000 description 17
- 239000004615 ingredient Substances 0.000 description 16
- 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 15
- 150000003839 salts Chemical class 0.000 description 15
- 239000003760 tallow Substances 0.000 description 15
- 125000000217 alkyl group Chemical group 0.000 description 13
- 239000007859 condensation product Substances 0.000 description 13
- 235000014113 dietary fatty acids Nutrition 0.000 description 13
- 239000000194 fatty acid Substances 0.000 description 13
- 229930195729 fatty acid Natural products 0.000 description 13
- 150000004665 fatty acids Chemical class 0.000 description 12
- 238000012360 testing method Methods 0.000 description 12
- 229910052783 alkali metal Inorganic materials 0.000 description 11
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 9
- 150000001340 alkali metals Chemical class 0.000 description 9
- 150000003863 ammonium salts Chemical class 0.000 description 9
- 125000000129 anionic group Chemical group 0.000 description 9
- 239000007844 bleaching agent Substances 0.000 description 9
- 238000004140 cleaning Methods 0.000 description 9
- 229910052700 potassium Inorganic materials 0.000 description 9
- 239000011591 potassium Substances 0.000 description 9
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 8
- 235000013162 Cocos nucifera Nutrition 0.000 description 8
- 244000060011 Cocos nucifera Species 0.000 description 8
- 230000000694 effects Effects 0.000 description 8
- 230000002209 hydrophobic effect Effects 0.000 description 8
- 235000019832 sodium triphosphate Nutrition 0.000 description 8
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 7
- 239000003240 coconut oil Substances 0.000 description 7
- 235000019864 coconut oil Nutrition 0.000 description 7
- 229910052938 sodium sulfate Inorganic materials 0.000 description 7
- 235000011152 sodium sulphate Nutrition 0.000 description 7
- 238000005406 washing Methods 0.000 description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 239000004115 Sodium Silicate Substances 0.000 description 6
- 238000009472 formulation Methods 0.000 description 6
- 229960001922 sodium perborate Drugs 0.000 description 6
- 239000012418 sodium perborate tetrahydrate Substances 0.000 description 6
- 159000000000 sodium salts Chemical class 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
- IBDSNZLUHYKHQP-UHFFFAOYSA-N sodium;3-oxidodioxaborirane;tetrahydrate Chemical compound O.O.O.O.[Na+].[O-]B1OO1 IBDSNZLUHYKHQP-UHFFFAOYSA-N 0.000 description 6
- YKLJGMBLPUQQOI-UHFFFAOYSA-M sodium;oxidooxy(oxo)borane Chemical compound [Na+].[O-]OB=O YKLJGMBLPUQQOI-UHFFFAOYSA-M 0.000 description 6
- 239000007787 solid Substances 0.000 description 6
- 229910019142 PO4 Inorganic materials 0.000 description 5
- 239000000654 additive Substances 0.000 description 5
- 150000008051 alkyl sulfates Chemical class 0.000 description 5
- 229910052757 nitrogen Inorganic materials 0.000 description 5
- UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 description 5
- 159000000001 potassium salts Chemical class 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 150000003254 radicals Chemical class 0.000 description 5
- 238000012216 screening Methods 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 4
- 230000000996 additive effect Effects 0.000 description 4
- 150000001298 alcohols Chemical class 0.000 description 4
- 125000003342 alkenyl group Chemical group 0.000 description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 4
- 239000002585 base Substances 0.000 description 4
- 239000007795 chemical reaction product Substances 0.000 description 4
- 125000003976 glyceryl group Chemical group [H]C([*])([H])C(O[H])([H])C(O[H])([H])[H] 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 239000001301 oxygen Substances 0.000 description 4
- 229910052760 oxygen Inorganic materials 0.000 description 4
- 235000021317 phosphate Nutrition 0.000 description 4
- 239000010452 phosphate Substances 0.000 description 4
- LCPVQAHEFVXVKT-UHFFFAOYSA-N 2-(2,4-difluorophenoxy)pyridin-3-amine Chemical compound NC1=CC=CN=C1OC1=CC=C(F)C=C1F LCPVQAHEFVXVKT-UHFFFAOYSA-N 0.000 description 3
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 238000004061 bleaching Methods 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 229940096386 coconut alcohol Drugs 0.000 description 3
- 238000009833 condensation Methods 0.000 description 3
- 230000005494 condensation Effects 0.000 description 3
- VTIIJXUACCWYHX-UHFFFAOYSA-L disodium;carboxylatooxy carbonate Chemical compound [Na+].[Na+].[O-]C(=O)OOC([O-])=O VTIIJXUACCWYHX-UHFFFAOYSA-L 0.000 description 3
- 239000008233 hard water Substances 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 3
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 3
- 229940045872 sodium percarbonate Drugs 0.000 description 3
- CHQMHPLRPQMAMX-UHFFFAOYSA-L sodium persulfate Substances [Na+].[Na+].[O-]S(=O)(=O)OOS([O-])(=O)=O CHQMHPLRPQMAMX-UHFFFAOYSA-L 0.000 description 3
- 150000003871 sulfonates Chemical class 0.000 description 3
- JAXNXAGNWJBENQ-UHFFFAOYSA-N 1-dimethylphosphoryldodecan-2-ol Chemical compound CCCCCCCCCCC(O)CP(C)(C)=O JAXNXAGNWJBENQ-UHFFFAOYSA-N 0.000 description 2
- DUIOKRXOKLLURE-UHFFFAOYSA-N 2-octylphenol Chemical compound CCCCCCCCC1=CC=CC=C1O DUIOKRXOKLLURE-UHFFFAOYSA-N 0.000 description 2
- AEDQNOLIADXSBB-UHFFFAOYSA-N 3-(dodecylazaniumyl)propanoate Chemical compound CCCCCCCCCCCCNCCC(O)=O AEDQNOLIADXSBB-UHFFFAOYSA-N 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical class OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
- 239000005977 Ethylene Substances 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 238000013019 agitation Methods 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 125000002947 alkylene group Chemical group 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical class [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 2
- 125000002091 cationic group Chemical group 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- SYELZBGXAIXKHU-UHFFFAOYSA-N dodecyldimethylamine N-oxide Chemical compound CCCCCCCCCCCC[N+](C)(C)[O-] SYELZBGXAIXKHU-UHFFFAOYSA-N 0.000 description 2
- SUMDYPCJJOFFON-UHFFFAOYSA-N isethionic acid Chemical compound OCCS(O)(=O)=O SUMDYPCJJOFFON-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 230000014759 maintenance of location Effects 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- IBOBFGGLRNWLIL-UHFFFAOYSA-N n,n-dimethylhexadecan-1-amine oxide Chemical compound CCCCCCCCCCCCCCCC[N+](C)(C)[O-] IBOBFGGLRNWLIL-UHFFFAOYSA-N 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 235000019198 oils Nutrition 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
- MPQXHAGKBWFSNV-UHFFFAOYSA-N oxidophosphanium Chemical group [PH3]=O MPQXHAGKBWFSNV-UHFFFAOYSA-N 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 239000002689 soil Substances 0.000 description 2
- 230000003381 solubilizing effect Effects 0.000 description 2
- DIORMHZUUKOISG-UHFFFAOYSA-N sulfoformic acid Chemical compound OC(=O)S(O)(=O)=O DIORMHZUUKOISG-UHFFFAOYSA-N 0.000 description 2
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 2
- 125000004434 sulfur atom Chemical group 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 238000005303 weighing Methods 0.000 description 2
- FLIVPMQIZYUQBE-UHFFFAOYSA-N (3-dodecoxy-2-hydroxypropyl)-ethyl-propylsulfanium Chemical compound CCCCCCCCCCCCOCC(O)C[S+](CC)CCC FLIVPMQIZYUQBE-UHFFFAOYSA-N 0.000 description 1
- NYEOFIBTYDEESJ-UHFFFAOYSA-N 1-[2-[2-(2-dimethylphosphorylethoxy)ethoxy]ethoxy]nonane Chemical compound CCCCCCCCCOCCOCCOCCP(C)(C)=O NYEOFIBTYDEESJ-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
- QYRXERZWYVOCEQ-UHFFFAOYSA-N 1-methylsulfinyloctadecane Chemical compound CCCCCCCCCCCCCCCCCCS(C)=O QYRXERZWYVOCEQ-UHFFFAOYSA-N 0.000 description 1
- NCBIQCVXOJNNEI-UHFFFAOYSA-N 2-dodecoxy-n,n-dimethylethanamine oxide Chemical compound CCCCCCCCCCCCOCC[N+](C)(C)[O-] NCBIQCVXOJNNEI-UHFFFAOYSA-N 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
- QOXOZONBQWIKDA-UHFFFAOYSA-N 3-hydroxypropyl Chemical group [CH2]CCO QOXOZONBQWIKDA-UHFFFAOYSA-N 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- VCCWZAQTNBYODU-UHFFFAOYSA-N CC(=C)CC(C)CCC(C)=C Chemical group CC(=C)CC(C)CCC(C)=C VCCWZAQTNBYODU-UHFFFAOYSA-N 0.000 description 1
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- 241000283153 Cetacea Species 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-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
- 229930194542 Keto Natural products 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- SUZRRICLUFMAQD-UHFFFAOYSA-N N-Methyltaurine Chemical compound CNCCS(O)(=O)=O SUZRRICLUFMAQD-UHFFFAOYSA-N 0.000 description 1
- 241000047703 Nonion Species 0.000 description 1
- 235000019482 Palm oil 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
- 229910007541 Zn O Inorganic materials 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 229910000288 alkali metal carbonate Inorganic materials 0.000 description 1
- 150000008041 alkali metal carbonates Chemical class 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 125000005210 alkyl ammonium group Chemical group 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 1
- 235000003704 aspartic acid Nutrition 0.000 description 1
- 239000010480 babassu oil Substances 0.000 description 1
- 150000001642 boronic acid derivatives Chemical class 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride 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
- 150000007942 carboxylates Chemical class 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 238000012937 correction Methods 0.000 description 1
- 230000008021 deposition Effects 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
- 229960001760 dimethyl sulfoxide Drugs 0.000 description 1
- 235000011180 diphosphates Nutrition 0.000 description 1
- BHDAXLOEFWJKTL-UHFFFAOYSA-L dipotassium;carboxylatooxy carbonate Chemical compound [K+].[K+].[O-]C(=O)OOC([O-])=O BHDAXLOEFWJKTL-UHFFFAOYSA-L 0.000 description 1
- NORJLCYHZCPMBS-UHFFFAOYSA-N dodecyl-dimethyl-propylphosphanium Chemical compound CCCCCCCCCCCC[P+](C)(C)CCC NORJLCYHZCPMBS-UHFFFAOYSA-N 0.000 description 1
- JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecylamine Chemical compound CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 235000019197 fats Nutrition 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 229940013317 fish oils Drugs 0.000 description 1
- 125000001153 fluoro group Chemical group F* 0.000 description 1
- 229940083124 ganglion-blocking antiadrenergic secondary and tertiary amines Drugs 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 230000002070 germicidal effect Effects 0.000 description 1
- 125000005456 glyceride group Chemical group 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 239000004519 grease Substances 0.000 description 1
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 125000001165 hydrophobic group Chemical group 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 229940045996 isethionic acid Drugs 0.000 description 1
- 230000002045 lasting effect Effects 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 125000000325 methylidene group Chemical class [H]C([H])=* 0.000 description 1
- ONHFWHCMZAJCFB-UHFFFAOYSA-N myristamine oxide Chemical compound CCCCCCCCCCCCCC[N+](C)(C)[O-] ONHFWHCMZAJCFB-UHFFFAOYSA-N 0.000 description 1
- JEJSGFPNNFSSNI-UHFFFAOYSA-N n,n-bis(2-hydroxyethyl)tetradecan-1-amine oxide Chemical compound CCCCCCCCCCCCCC[N+]([O-])(CCO)CCO JEJSGFPNNFSSNI-UHFFFAOYSA-N 0.000 description 1
- HUQYGHSBSCVCQT-UHFFFAOYSA-N n,n-diethyl-2-[2-(2-octoxyethoxy)ethoxy]ethanamine oxide Chemical compound CCCCCCCCOCCOCCOCC[N+]([O-])(CC)CC HUQYGHSBSCVCQT-UHFFFAOYSA-N 0.000 description 1
- YWWNNLPSZSEZNZ-UHFFFAOYSA-N n,n-dimethyldecan-1-amine Chemical compound CCCCCCCCCCN(C)C YWWNNLPSZSEZNZ-UHFFFAOYSA-N 0.000 description 1
- RSVIRMFSJVHWJV-UHFFFAOYSA-N n,n-dimethyloctan-1-amine oxide Chemical compound CCCCCCCC[N+](C)(C)[O-] RSVIRMFSJVHWJV-UHFFFAOYSA-N 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- ZCYXXKJEDCHMGH-UHFFFAOYSA-N nonane Chemical compound CCCC[CH]CCCC ZCYXXKJEDCHMGH-UHFFFAOYSA-N 0.000 description 1
- BKIMMITUMNQMOS-UHFFFAOYSA-N normal nonane Natural products CCCCCCCCC BKIMMITUMNQMOS-UHFFFAOYSA-N 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000002540 palm oil Substances 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 125000002467 phosphate group Chemical group [H]OP(=O)(O[H])O[*] 0.000 description 1
- XYFCBTPGUUZFHI-UHFFFAOYSA-O phosphonium Chemical compound [PH4+] XYFCBTPGUUZFHI-UHFFFAOYSA-O 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 125000004437 phosphorous atom Chemical group 0.000 description 1
- 229910052698 phosphorus Inorganic materials 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
- 229920001983 poloxamer Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 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
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000003449 preventive effect Effects 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- KCXFHTAICRTXLI-UHFFFAOYSA-M propane-1-sulfonate Chemical compound CCCS([O-])(=O)=O KCXFHTAICRTXLI-UHFFFAOYSA-M 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 229940045998 sodium isethionate Drugs 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
- 239000008234 soft water Substances 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 230000001180 sulfating effect Effects 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 238000005494 tarnishing Methods 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-O triethanolammonium Chemical class OCC[NH+](CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-O 0.000 description 1
- JEVFKQIDHQGBFB-UHFFFAOYSA-K tripotassium;2-[bis(carboxylatomethyl)amino]acetate Chemical class [K+].[K+].[K+].[O-]C(=O)CN(CC([O-])=O)CC([O-])=O JEVFKQIDHQGBFB-UHFFFAOYSA-K 0.000 description 1
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- 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
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D19/00—Degasification of liquids
- B01D19/02—Foam dispersion or prevention
- B01D19/04—Foam dispersion or prevention by addition of chemical substances
- B01D19/0404—Foam dispersion or prevention by addition of chemical substances characterised by the nature of the chemical substance
- B01D19/0418—Foam dispersion or prevention by addition of chemical substances characterised by the nature of the chemical substance compounds containing P-atoms
-
- 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
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/08—Esters of oxyacids of phosphorus
- C07F9/09—Esters of phosphoric acids
- C07F9/091—Esters of phosphoric acids with hydroxyalkyl compounds with further substituents on alkyl
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/0005—Other compounding ingredients characterised by their effect
- C11D3/0026—Low foaming or foam regulating compositions
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/36—Organic compounds containing phosphorus
- C11D3/367—Organic compounds containing phosphorus containing halogen
- C11D3/368—Organic compounds containing phosphorus containing halogen containing fluorine
-
- 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
- C11D9/00—Compositions of detergents based essentially on soap
- C11D9/04—Compositions of detergents based essentially on soap containing compounding ingredients other than soaps
- C11D9/22—Organic compounds, e.g. vitamins
- C11D9/34—Organic compounds, e.g. vitamins containing phosphorus
Definitions
- ABSTRACT OF THE DISCLOSURE Low to medium sudsing heavy duty detergent compositions containing a soap or non-soap synthetic detergent, a detergent builder and a fluoroalkyl suds suppressing agent.
- This invention relates to heavy duty detergent compositions. More particularly, the present invention relates to low to medium sudsing built detergent compositions containing a soap or non-soap synthetic detergent to impart good cleaning characteristics and a fiuoralkyl suds suppressing agent to suppress the suds which are created by the active organic detergent at high wash water temperatures; particularly at wash water temperatures in excess of about 160 F.
- ingredients which are combined in the built detergent formulations of this invention are very briefly described below. These ingredients are all known individually but they have not heretofore been utilized in the manner disclosed in this invention to produce low to medium sudsing heavy duty built detergent compositions.
- Tumbler type washing machines differ from the conventional top loading automatic washers which are in general use in the United States.
- the tumblers or rotating drum machines require substantially less water than the top loading automatics. Only about one half to one quarter amount of water is used to operate a tumbler.
- Most tumblers (particularly those rotating drum machines found throughout Europe) also heat their own water. Cold water is put into the machines from the tap or other water source and is heated either electrically or by gas to the desired temperature. This temperature is generally higher than that of hot water drawn from the faucet. Water used in a tumbler type washing machine is ordinarily heated in the machine to about 160 F. to about 212 F. The hottest hot water tap temperature seldo'm exceeds about 150 F.
- compositions of this invention are low to medium sudsing heavy-duty detergent compositions designed pri marily for use in tumbler type washing machines.
- soap as used herein is meant to designate alkali metal soaps and those useful in the present invention are further defined hereinafter.
- non-soap synthetic detergents useful in the present invention can be selected from the group consisting of anionic, nonionic, zwitterionic and amphoteric detergents.
- the anionic synthetic detergents can be broadly described as the water-soluble salts, including the alkali metal, ammonium and substituted ammonium salts, of organic sulfuric reaction products having in their 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 nonionic synthetic detergents may be broadly defined as compounds produced by condensation of alkylene oxide groups (hydrophilic in nature) with an organic hydrophobic compound which may be aliphatic or alkyl aromatic in nature.
- the length of thehydrophilic or polyoxyalkylene radical which is condensed with any particular hydrophobic group can be readily adjusted to yield a water-soluble compound having the desired degree of balance between hydrophilic and hydrophobic elements.
- the zwitterionic detergents such as betaines and sultaines and similar compounds are compounds wherein the molecule contains both basic and acidic groups which form within the salt giving the molecule both cationic and anionic hydrophilic groups over a broad range of wash water pH values.
- the amphoteric detergents can be either cationic or anionic depending upon the pH of the system and are further defined hereinafter.
- the fluoroalkyl suds suppressors are compounds of the general formula R PO(OM) as fully described hereinafter. Certain of the compounds of the above general formula have been suggested for a variety of purposes including use as leveling agents, as oil repellants, as lubricating agents for aqueous systems and as ingredients in rust preventive formulations.
- compositions comprise by weight from about 2% to about 30%, and preferably from about 4% to about 15%, of a detergent selected from the aforementioned group consisting of soap and non-soap synthetic detergents and mixtures thereof; from about 2% to about 65%, and preferably from about 6% to about 45% of a detergent builder and from about 0.1% to about 8%, preferably from about 1% to about 3% of a fluoroalkyl suds suppressing agent of the class described herein.
- the soaps useful in the present invention are the alkali metal soaps such as the sodium and potassium salts of the higher fatty acids of naturally occurring plant or animal esters, e.g., palm oil, coconut oil, babassu oil, soybean oil, castor oil, tallow, whale and fish oils, grease and lard and mixtures thereof.
- Sodium and potassium soaps can be made by direct saponification of the fats and oils or by the neutralization of the fatty acids which are prepared in a separate manufacturing process.
- Suitable soaps are the sodium, potassium, ammonium and alkylolammonium salts of higher 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.
- Synthetic detergents (a) Anionic detergent (excluding true soaps).
- the anionic synthetic detergents of this present invention are as described above.
- Important examples of the synthetic detergents which form a part of the preferred compositions of the present invention are the following: as alkali metal (e.g., sodium and potassium) ammonium and substituted ammonium (e.g., lower alkyl ammonium) salts; alkyl sulfates, especially those obtained by sulfating the higher alcohols produced by reducing the glycerides of tallow or coconut oil; random paratfin sulfonates, in which the alkyl group contains from about 8 to about 22 carbon atoms, preferably from about 14 to about 18 carbon atoms, prepared by treating random parafiin hydrocarbons in sulfur dioxide and chlorine in the presence of light followed by treating with a base; branched or linear alkyl benzene sulfonates, in which the alkyl group contains from about 8 to about 18 carbon atoms,
- Preferred anionics include the alkyl sulfates and the random parafiin sulfonates.
- Nonionic synthetic deteregnts (b) Nonionic synthetic deteregnts.This class of synthetic detergents may be broadly defined as above.
- Pluronic a well known class of nonionic synthetic detergents is made available on the market under the trade name of Pluronic. These compounds are formed by condensing ethylene oxide with a hydrophobic base formed by the condensation of propylene oxide with propylene glycol.
- the hydrophobic portion of the molecule which, of course, exhibits water insolubility has a molecular weight of from about 1500 to 1800.
- the addition of polyoxyethylene radicals to this hydrophobic portion tends to increase the water solubility of the molecule as a whole and the liquid character of the products is retained up to the point where polyoxyethylene content is about 50% of the total weight of the condensation product.
- nonionic synthetic detergents include:
- the polyethylene oxide condensates of alkyl phenols, e.g., the condensation products of alkyl phenols having an alkyl group containing from about 6 to 12 carbon atoms in either a straight chain or branched chain configuration, with ethylene oxide, the said ethylene oxide being present in amounts equal to 10 to moles of ethylene oxideper mole of alkyl phenol.
- the alkyl substituent in such compounds may be derived from polymerized propylene, diisobutylene, octane, or nonane, for example.
- R R R N+O Long chain tertiary amine oxides corresponding to the following general formula, R R R N+O, wherein R contains an alkyl, alkenyl or monohydroxy alkyl radical of from about 8 to about 18 carbon atoms, from 0 to about 10 ethylene oxide moieties, and from 0 to 1 glyceryl moiety, and R and R contain from 1 to about 3 carbon atoms and from 0 to about 1 hydroxy group, e.g., methyl, ethyl, propyl, hydroxy ethyl, or hydroxy propyl radicals.
- amine oxides suitable for use in this invention include dimethyldodecyl amine oxide, oleyldi(2-hydroxyethyl) amine oxide, dimethyloctylamine oxide, dimethyldecylamine, oxide dimethyltetradecylamine oxide, 3,6,9-trioxaheptadecyldiethylamine oxide, di(2-hydroxyethyl) tetradecylamine oxide, 2-dodecoxy ethyl dimethylamine oxide, 3- dodecoxy-Z-hydroxy propyl di(3-hydroxypropyl) amine oxide, dimethylhexadecylamine oxide.
- R contains an alkyl, alkenyl, or hydroxy alkyl radical of from about 8 to about 18 carbon atoms, from 0 to about 10 ethylene oxide moieties and from O to 1 glyceryl moiety;
- Y is selected from the group consisting of nitrogen, phosphorous, and sulfur atoms;
- R is an alkyl or monohydroxy alkyl group containing 1 to about 3 carbon atoms;
- x is 1 when y is a sulfur atom and 2 when Y is a nitrogen or phosphorous atom,
- R is an alkylene or hydroxy alkylene of from 1 to about 4 carbon atoms and
- Z is a radical selected from the group consisting of carboxylate, sulfonate, sulfate, phosphonate, and phosphate groups.
- Amphoteric synthetic detergents This group of 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, sodium 3-dodecylaminopropane sulfonate, dodecyl-beta-alamine, N-alkyltaurines such as the one prepared by reacting dodecylamine with sodium isethionate according to the teaching of US. 2,658,072, N-higher alkyl aspartic acids such as those produced according to the teaching of US. 2,438,091, and the products sold under the trade name Mirano and described in US. Pat. 2,528,378.
- detergent builders useful in the present invention are water-soluble inorganic alkaline builder salts and organic alkaline sequestering builder salts and mixtures thereof as described and illustrated below.
- water soluble inorganic alkaline builder salts which are used in the compositions of this invention include the sodium, potassium, ammonium and substituted ammonium salts of the alkali metal carbonates, borates, phosphates, condensed polyphosphates, bicarbonates and silicates.
- Specific examples of such salts are the sodium and potassium tripolyphosphates, carbonates, tetraborates, pyrophosphates, orthophosphates, bicarbonates and hexametaphosphates.
- organic alkaline builder salts examples include the alkali metal, ammonium or substituted ammonium aminopolycarboxylates; for example: sodium and potassium N-(s-hydroxyethyl)-ethylenediaminetriacetates and sodium and potassium nitrilotriacetates.
- alkali metal, ammonium or substituted ammonium aminopolycarboxylates for example: sodium and potassium N-(s-hydroxyethyl)-ethylenediaminetriacetates and sodium and potassium nitrilotriacetates.
- Other valuable polycarboxylate builders are the sodium and potassium salts of polymaleate, polyitaconate, and polyacrylate.
- the alkali metal salts of phytic acid are also suitable builders.
- the polyphosphonates which can be used as builders for the compositions of this invention include compounds exemplified by the following: sodium and potassium salts of ethane-l-hydroxy-l, l-diphosphonate, sodium and potassium salts of methylene and ethylenediphosphonates as well as the alkali metal salts of such compounds.
- Fluoroalkyl suds suppressing agent The fluoroalkyl compounds useful in the present invention as suds suppressing agents have the following general formula:
- the fluoroalkyl suds suppressors of the present invention can be utilized alone or in combination and include both the free acid and water soluble salt forms.
- fiuoroalkyl suds suppressors refers to both the acid and water soluble salt forms.
- Operable salts include the alkali metal (e.g., sodium and potassium), ammonium and substituted ammonium (e.g., mono-, di-, and triethanolammonium) salts.
- Preferred compounds of this class contain in their alkyl structure a straight chain of at least 2 carbon atoms and not less than 4 fluorine atoms. Examples of such preferred structures include the following:
- fluoroalkyl suds suppressing agents of the present invention are compounds commercially available from E. I. du Pont de Nemours & Company under the trade name Zonyl. Additional ex amples of operable fluoroalkyl suds suppressors and methods for their preparation, are disclosed by Benning in U.S. Pat. 2,559,749 and by Brace and MacKenZie in US. Pat. 3,083,224, said patents being incorporated herein by reference.
- the fiuoroalkyl suds suppressing agents can be used in amounts ranging from about 0.1% to about 8.0% by weight of the total composition. Amounts of less than about 0.1% do not give desirable suds suppressing effects whereas amounts greater than 8% do not appear to produce any greater effect than is attainable with lesser concentrations, thus utilization of such higher amounts is uneconomical and serves no purpose. Preferably the amount is from about 1% to about 3%.
- a preferred embodiment of the present invention contains from about 1% to about 50% by weight of a per compound bleaching agent, such as sodium perborate.
- the per compound bleaching agent imparts a high level of cleaning and bleaching power to the compositions particularly when used in conjunction with the builder materials described above.
- Other per compounds which can be used in place of the sodium perborate or in addition thereto include compounds such as sodium percarbonate and sodium persulfate.
- the potassium and substituted ammonium salts can also be used.
- the per compounds derive their bleaching power from the release of active oxygen in solution.
- Sodium perborate is the preferred per compound bleaching agent. From about %to about is the preferred range of usage of the per compound bleaching agent.
- a further preferred embodiment includes in the detergent part of the compositions of the present invention from about 0.5% to about 6%, preferably from about 1% to about 3% of a nonionic condensation product.
- a nonionic condensation product aids in reducing the suds level.
- the compounds are the condensation product of aliphatic alcohols having from about 12 to about 22 carbon atoms, in either a straight chain or a branched chain configuration, with ethylene oxide.
- a typical example is a tallow alcohol-ethylene oxide condensate having from about 5 to about 30 moles (or up to about moles) of ethylene oxide per mole of tallow alcohol.
- Preferred compounds include tallow alcohol-ethylene oxide condensation product containing 11 moles of ethylene oxide per mole of tallow alcohol.
- the term tallow as used herein and in the accompanying examples indicates a carbon chain length distribution approximately as follows: 2.5% C 28%C 23%C 2% palmitoleic, 41.5% oleic and 3% linoleic (the first three fatty acids are saturated).
- coconut for example, in a coconut alcohol-ethylene oxide condensation product
- coconut alcohol-ethylene oxide condensation product applies to a distribution of carbon chain lengths which is approximately as follows: 8%03, 7%C10, 48%012, 17% 14! 9%C16, C 7% oleic and 2% linoleic (the first six fatty acids listed are saturated).
- compositions of this invention it is essential that the proportion of the ingredients set forth above be observed.
- the principal object of this invention is observed, i.e., control of the sudsing level attributed in part to sudsing of the organic detergent ingredient which is aggravated by oxygen evolution from any per compound bleaching agent employed in the system.
- the suds control mechanism of the fluoroalkyl suds suppressor is not materially affected by the water hardness. It is well known that most prior art suds suppressor agents, such as fatty acids and fatty acid soaps lose some of their effectiveness in hard water.
- An additional advantage of the present invention is the excellent whiteness maintenance that the compositions provide. Many suds suppressors are insoluble and deposit on articles washed with compositions containing them leading, to a decrease in the whiteness of the articles.
- the compositions of this invention containing the fluoroalkyl suds suppressing agents indicate no such deposition problems.
- compositions of this invention are preferably employed in the form of complete detergent formulations.
- complete detergent formulations can be prepared in any of several forms including granular, flake, liquid or tablet.
- compositions can contain particulate inorganic salts which are inert to the formula to act as fillers.
- examples of such salts include sodium sulfate and sodium chloride.
- compositions of the present invention can also con tain adjuvants, diluents, soil suspending agents such as carboxymethylcellulose and additives including germicidal agents, enzymes, anti-tarnishing agents, optical brightners and dyes.
- additional miscellaneous ingredients can be employed in amounts about 10% by weight of the composition.
- compositions of this invention can be prepared in any suitable manner as long as the proportions set forth herein are followed. Numerous methods are known in the art for preparing such compositions; for instance, ingredients can be mechanically admixed, spray-dried or agglomerated according to the stated proportions.
- the evaluation procedure to which reference is made in the following examples is a method which was developed to determine the suds profile of low sudsing detergent formulations. These tests are conducted in four smaller than normal (about scale), specially designed, horizontally rotating drum washing machines which operate simultaneously and simulate as closely as possible the agitation, temperature control, product concentration, and water conditions of an actual tumbler type washing machine in operation. The machines are so designed (with a transparent front) that the suds heights and water temperatures can be visually observed and recorded throughout any specific test. Cloths to be tested are worn by panelists and distributed so that equal amounts of naturally soiled fabrics are washed in each machine. The load comprises two T-shirts weighing about 200 grams and nine socks weighing about 200 grams.
- a standard test includes two periods which differ only in temperature and concentration of the detergent compositions. The temperatures are higher and the concentrations greater in the second period. During the first washing period lasting ten minutes, the water temperature is raised from 60 F. to about F. by the heaters which are built into the machine. A portion of the wash solution is then removed from the machines and replaced by an equal quantity of hard water and a weight of detergent composition equal to the amount added for the first period. This represents the second period as referred to below and the temperature is raised to about F.
- the suds levels and temperatures are recorded at least every two minutes. In this way the actual use and fall, if any, of the suds in response to the soil load, water hardness, product formulation, and increase in temperature can be observed. It takes approximately twenty minutes after the second period is begun for the water in the machines to reach 190 F.
- the machines are designed to be operated with about three liters of water. Soft water is adjusted to the desired hardness, about 15 grains per gallon, by the A detergent composition containing the following ingredients was prepared in the manner explained below.
- the sudsing characteristics of this composition were determined in the laundry screening test as described above. Temperature and suds heights were taken at two minute intervals during the second period and the results recorded. In conducting the test, 18 grams of the above composition were added to three liters of water containing about 400 grams of naturally soiled cloths. A ten minute first period was followed by replacement of 1.2 liters of the solution with an equal amount of clean hard water and an additional 18 grams of the detergent composition. Heat and agitation were supplied for a second period of 40 minutes. The hardness of the water was adjusted to gr./liter by the addition of calcium chloride.
- the term average indicates that a mixture of suds suppressing agents was utilized. This suds suppressing mixture was added to the powdered ingredients of the basic detergent composition in a methanol solution and the methanol allowed to evaporate completely before the testing began.
- Table 1 shows the elfect of the suds suppressing agents of the present invention. (In Table I and subsequent tables, the suds heights are reported at equal temperature intervals rather than the two minute intervals at which they were recorded to permit a more direct comparison of the results.)
- Table I shows the suds suppressing effect of the detergent compositions containing the suds suppressing agents over the detergent compositions that do not contain these agents.
- Table II clearly shows the advantageous effect of the detergent compositions containing the suds suppressing agents.
- a nonion'ic condensation product e.g., tallow alcohol-ethylene oxide condensation product containing an average of 11 moles of ethylene oxide
- a further reduction in suds height is noted.
- Example I containing the fiuoroalkyl suds suppressing agent when any of the following detergents are P substituted on an equal weight basis for the sodium salt of tallow alkyl sulfate in Example 1:
- Example I i.e., low to medium sudsing and good cleaning when the sodium perborate tetrahydrate is replaced on an equal weight basis by sodium percarbonate or sodium persulfate.
- EXAMPLE II The detergent composition set forth below was prepared in the manner described in Example I and the sudsing characteristics evaluated by the same laundry screening test.
- the suds suppressing agent utilized was H (CF CH -OPO (OH 2 when H (CF 7CH2 OPO (OH) 2 are substituted on an equal weight basis for the fluoroalkyl suds suppressing agent of Example II substantially equivalent suds suppressing results are obtained.
- the detergent composition described below was prepared in the manner described in Example I.
- the detergent composition described below was prepared in the manner described in Example I.
- a special embodiment of the present invention comprises the use of a non-soap synthetic detergent as the detergent component of the composition.
- a low to medium-sudsing laundry detergent composition consisting essentially of, by Weight, from about 2% to about 30% of a detergent selected from the group consisting of alkali metal soaps; anionic, non-soap synthetic detergents; nonionic, non-soap synthetic detergents; zwitterionic, non-soap synthetic detergents and amphoteric, non-soap synthetic detergents; from about 2% to about 65% of a detergent builder selected from the group consisting of water-soluble inorganic alkaline builder salts, organic alkaline sequestering builder salts and mixtures thereof; and from about 0.1% to about 8% of a fluoroalkyl suds suppressing agent of the general formula wherein R is selected from the group consisting of 3.
- composition of claim 2 wherein the fluoroalkyl suds suppressing agent is H'(CF CH -OPO (OH) 2 4.
- non-soap 1 1- synthetic detergent is the sodium salt of an alkyl sulfate wherein the alkyl group contains from about 8 to about 18 carbon atoms and mixtures thereof.
- composition of claim 1 wherein the non-soap synthetic detergent is the sodium salt of a random paraffin sulfonate containing an average of from about 10 to about 20 carbon atoms.
- composition of claim 1 wherein the detergent is a mixture of tallow and coconut soaps in a ratio of about 4:1.
- composition of claim 1 containing from about 1% to about 50% by weight of a per compound bleaching agent selected from the group consisting of sodium perborate, sodium percarbonate, sodium persulfate, potassum perborate, potassium percarbonate, potassium persulfate, substituted ammonium perborate, substituted ammonium percarbonate and substituted ammonium persulfate.
- a per compound bleaching agent selected from the group consisting of sodium perborate, sodium percarbonate, sodium persulfate, potassum perborate, potassium percarbonate, potassium persulfate, substituted ammonium perborate, substituted ammonium percarbonate and substituted ammonium persulfate.
- composition of claim 10 wherein the per compound bleaching agent is sodium perborate and the builder is sodium tripolyphosphate.
- composition of claim 1 wherein the detergent is a mixture of detergents containing from about 0.5% to about 6% by weight of the nonionic condensation product of alcohols having from 8 to 18 carbon atoms with 1030 moles of ethylene oxide.
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Abstract
LOW TO MEDIUM SUDSING HEAVY DUTY DETERGENT COMPOSITIONS CONTAINING A SOAP OR NON-SOAP SYNTHETIC DETERGENT, A DETERGENT BUILDER AND A FLUOROALKYL SUDS SUPPRESSING AGENT.
Description
ABSTRACT OF THE DISCLOSURE Low to medium sudsing heavy duty detergent compositions containing a soap or non-soap synthetic detergent, a detergent builder and a fluoroalkyl suds suppressing agent.
BACKGROUND OF THE INVENTION This invention relates to heavy duty detergent compositions. More particularly, the present invention relates to low to medium sudsing built detergent compositions containing a soap or non-soap synthetic detergent to impart good cleaning characteristics and a fiuoralkyl suds suppressing agent to suppress the suds which are created by the active organic detergent at high wash water temperatures; particularly at wash water temperatures in excess of about 160 F.
By way of background, the ingredients which are combined in the built detergent formulations of this invention are very briefly described below. These ingredients are all known individually but they have not heretofore been utilized in the manner disclosed in this invention to produce low to medium sudsing heavy duty built detergent compositions.
It is well recognized that heavy duty laundry detergents designed for use in tumbler or rotating drum type washing machines must possess a high degree of cleaning power but they must also be relatively low sudsing. Heretofore it has not been possible to formulate low to medium sudsing detergents compositions having good cleaning properties containing only low sudsing detergents, such as certain specific nonionic detergents. When other detergents have been added to one of these low to medium sudsing compositions to increase its cleaning efficiency, the sudsing level has increased to the point at which the composition was no longer useful for tumbler type machines. Furthermore, if a per compound bleaching agent has been added to one of these low to medium sudsing compositions to increase its bleaching efiiciency, the suds are greatly accentuated by the oxygen which is released by the per compound at high wash water temperatures.
Tumbler type washing machines differ from the conventional top loading automatic washers which are in general use in the United States. The tumblers or rotating drum machines require substantially less water than the top loading automatics. Only about one half to one quarter amount of water is used to operate a tumbler. Most tumblers (particularly those rotating drum machines found throughout Europe) also heat their own water. Cold water is put into the machines from the tap or other water source and is heated either electrically or by gas to the desired temperature. This temperature is generally higher than that of hot water drawn from the faucet. Water used in a tumbler type washing machine is ordinarily heated in the machine to about 160 F. to about 212 F. The hottest hot water tap temperature seldo'm exceeds about 150 F.
nited States: Patent Patented June 15, 1971 ice In operating a rotating drum type machine it is essen tial that the water and suds level be kept down in order to clean the clothes in the machine efficiently and to avoid oversudsing. The common manifestation of oversudsing in a rotating drum machine is suds coming out of the machine and flowing onto the floor.
SUMMARY OF THE INVENTION The compositions of this invention are low to medium sudsing heavy-duty detergent compositions designed pri marily for use in tumbler type washing machines.
The term soap as used herein is meant to designate alkali metal soaps and those useful in the present invention are further defined hereinafter.
The non-soap synthetic detergents useful in the present invention can be selected from the group consisting of anionic, nonionic, zwitterionic and amphoteric detergents.
The anionic synthetic detergents can be broadly described as the water-soluble salts, including the alkali metal, ammonium and substituted ammonium salts, of organic sulfuric reaction products having in their 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 nonionic synthetic detergents may be broadly defined as compounds produced by condensation of alkylene oxide groups (hydrophilic in nature) with an organic hydrophobic compound which may be aliphatic or alkyl aromatic in nature. The length of thehydrophilic or polyoxyalkylene radical which is condensed with any particular hydrophobic group can be readily adjusted to yield a water-soluble compound having the desired degree of balance between hydrophilic and hydrophobic elements.
The zwitterionic detergents such as betaines and sultaines and similar compounds are compounds wherein the molecule contains both basic and acidic groups which form within the salt giving the molecule both cationic and anionic hydrophilic groups over a broad range of wash water pH values. The amphoteric detergents can be either cationic or anionic depending upon the pH of the system and are further defined hereinafter.
The fluoroalkyl suds suppressors are compounds of the general formula R PO(OM) as fully described hereinafter. Certain of the compounds of the above general formula have been suggested for a variety of purposes including use as leveling agents, as oil repellants, as lubricating agents for aqueous systems and as ingredients in rust preventive formulations.
The sudsing propensities of the active synthetic detergents are suppressed by the fluoroalkyl suds suppressing agent. Compositions comprise by weight from about 2% to about 30%, and preferably from about 4% to about 15%, of a detergent selected from the aforementioned group consisting of soap and non-soap synthetic detergents and mixtures thereof; from about 2% to about 65%, and preferably from about 6% to about 45% of a detergent builder and from about 0.1% to about 8%, preferably from about 1% to about 3% of a fluoroalkyl suds suppressing agent of the class described herein.
The compounds comprising the compositions of this invention are fully characterized below:
(1) Natural soaps The soaps useful in the present invention are the alkali metal soaps such as the sodium and potassium salts of the higher fatty acids of naturally occurring plant or animal esters, e.g., palm oil, coconut oil, babassu oil, soybean oil, castor oil, tallow, whale and fish oils, grease and lard and mixtures thereof. Sodium and potassium soaps can be made by direct saponification of the fats and oils or by the neutralization of the fatty acids which are prepared in a separate manufacturing process. Examples of suitable soaps are the sodium, potassium, ammonium and alkylolammonium salts of higher 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.
(2) Synthetic detergents (a) Anionic detergent (excluding true soaps).The anionic synthetic detergents of this present invention are as described above. Important examples of the synthetic detergents which form a part of the preferred compositions of the present invention are the following: as alkali metal (e.g., sodium and potassium) ammonium and substituted ammonium (e.g., lower alkyl ammonium) salts; alkyl sulfates, especially those obtained by sulfating the higher alcohols produced by reducing the glycerides of tallow or coconut oil; random paratfin sulfonates, in which the alkyl group contains from about 8 to about 22 carbon atoms, preferably from about 14 to about 18 carbon atoms, prepared by treating random parafiin hydrocarbons in sulfur dioxide and chlorine in the presence of light followed by treating with a base; branched or linear alkyl benzene sulfonates, in which the alkyl group contains from about 8 to about 18 carbon atoms, preferably from about 10 to about 14 carbon atoms, especially those of the types described in US. Pat. Nos. 2,220,099, and 2,477,383; sodium alkyl glyceryl ether sulfonates, especially those ethers of the higher alcohols derived from tallow and coconut oil; coconut oil fatty acid monoglyceride sulfates and sulfonates; sulfuric acid esters of the reaction product of one mole of a higher fatty alcohol (e.g., tallow or coconut alcohols) and from about 1 to about 6, preferably about 3 moles of ethylene oxide; alkyl phenol ethylene oxide ether sulfates with about 4 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; fatty acid amides of the methyl taurine in which the fatty acids, for example, are derived from coconut oil; sulfonated olefins of US. Pat. No. 3,332,880; and others known in the art, a number being specifically set forth in US. Pat. Nos. 2,486,921; 2,486,922 and 2,396,278.
Preferred anionics include the alkyl sulfates and the random parafiin sulfonates.
(b) Nonionic synthetic deteregnts.This class of synthetic detergents may be broadly defined as above.
For example, a well known class of nonionic synthetic detergents is made available on the market under the trade name of Pluronic. These compounds are formed by condensing ethylene oxide with a hydrophobic base formed by the condensation of propylene oxide with propylene glycol. The hydrophobic portion of the molecule which, of course, exhibits water insolubility has a molecular weight of from about 1500 to 1800. The addition of polyoxyethylene radicals to this hydrophobic portion tends to increase the water solubility of the molecule as a whole and the liquid character of the products is retained up to the point where polyoxyethylene content is about 50% of the total weight of the condensation product.
Other suitable nonionic synthetic detergents include:
(1) The polyethylene oxide condensates of alkyl phenols, e.g., the condensation products of alkyl phenols having an alkyl group containing from about 6 to 12 carbon atoms in either a straight chain or branched chain configuration, with ethylene oxide, the said ethylene oxide being present in amounts equal to 10 to moles of ethylene oxideper mole of alkyl phenol. The alkyl substituent in such compounds may be derived from polymerized propylene, diisobutylene, octane, or nonane, for example.
(2) Those derived from the condensation of ethylene oxide with the product resulting from the reaction of propylene oxide and ethylene diamineproducts which may be varied in composition depending upon the balance between the hydrophobic and hydrophilic elements which is desired. For example, compounds containing from about 40% to about polyoxyethylene by weight and having a molecular weight of from about 5000 to about 11,000 resulting from the reaction of ethylene oxide groups with a hydrophobic base constituted of the reaction product of ethylene diamine and excess propylene oxide, said base having a molecular weight of the order of 2500 to 3000, are satisfactory.
(3) The condensation product of aliphatic alcohols having from 8 to 18 carbon atoms, in either straight chain or branched chain configuration, with ethylene oxide, e.g., a coconut alcohol ethylene oxide condensate having from 10 to 30 moles of ethylene oxide per mole of coconut alcohol, the coconut alcohol fraction having from 10 to 14 carbon atoms.
(4) Long chain tertiary amine oxides corresponding to the following general formula, R R R N+O, wherein R contains an alkyl, alkenyl or monohydroxy alkyl radical of from about 8 to about 18 carbon atoms, from 0 to about 10 ethylene oxide moieties, and from 0 to 1 glyceryl moiety, and R and R contain from 1 to about 3 carbon atoms and from 0 to about 1 hydroxy group, e.g., methyl, ethyl, propyl, hydroxy ethyl, or hydroxy propyl radicals. The arrow in the formula is a conventional representation of a semi-polar bond, Examples of amine oxides suitable for use in this invention include dimethyldodecyl amine oxide, oleyldi(2-hydroxyethyl) amine oxide, dimethyloctylamine oxide, dimethyldecylamine, oxide dimethyltetradecylamine oxide, 3,6,9-trioxaheptadecyldiethylamine oxide, di(2-hydroxyethyl) tetradecylamine oxide, 2-dodecoxy ethyl dimethylamine oxide, 3- dodecoxy-Z-hydroxy propyl di(3-hydroxypropyl) amine oxide, dimethylhexadecylamine oxide.
(5) Long chain tertiary phosphine oxides corresponding to the following general formula RRRT O wherein R contains an alkyl, alkenyl or monohydroxyalkyl radical ranging from 8 to 18 carbon atoms in chain length, from 0 to about 10 ethylene oxide moieties and from 0 to l glyceryl moiety and R and R" are each alkyl or monohydroxyalkyl groups containing from 1 to 3 carbon atoms. The arrow in the formula is a conventional representation of a semi-polar bond. Examples of suitable phosphine oxides are:
dodecyldimethylphosphine oxide tetradecyldimethylphosphine oxide tetradecylmethylethylphosphine oxide 3,6,9-trioxaoctadecyldimethylphosphine oxide cetyldimethylphosphine oxide 3-dodecoxy-2-hydroxypropyldi (2-hydroxyethyl) phosphine oxide stearyldimethylphosphine oxide cetylethylpropylphosphine oxide oleyldiethylphosphine oxide dodecyldiethylphosphine oxide tetradecyldiethylphosphine oxide dodecyldipropylphosphine oxide dodecyldi (hydroxymethyl) phosphine oxide dodecyldi (Z-hydroxyethyl) phosphine oxide tetradecylmethyl-2-hydroxypropyl phosphine oxide oleyldimethylphosphine oxide 2-hydroxydodecyldimethylphosphine oxide (6) Long chain dialkyl sulfoxides containing one short chain alkyl or hydroxy alkyl radical of 1 to about 3 carbon atoms (usually methyl) and one long hydrophobic chain which contains alkyl, alkenyl, hydroxy alkyl, or keto alkyl radicals containing from about 8 to about 20 carbon atoms, from to about 10 ethylene oxide moieties and from 0 to 1 glyceryl moiety. Examples include:
octadecyl methyl sulfoxide, 2-ketotridecyl methyl sulfoxide 3,6,9-trioxaoctadecyl 2-hydroxyethyl sulfoxide dodecyl methyl sulfoxide oleyl 3-hydroxy propyl sulfoxide tetradecyl methyl sulfoxide 3-methoxytridecyl methyl sulfoxide 3-hydroxytridecy1 methyl sulfoxide 3-hydroxy-4-dodecoxybutyl methyl sulfoxide (c) Zwitterionic synthetic detergents.-This group of detergents can be broadly described as derivatives of aliphatic quaternary ammonium, phosphonium, and sulfonium compounds, in which the aliphatic radicals can be straight chain or branched, and wherein one of the aliphatic substituents contains from about 8 to 18 carbon atoms and one contains an anionic water solubilizing group, e.g., carboxy, sulfonate, sulfate, phosphate, or phosphonate. A general formula for these compounds is:
wherein R contains an alkyl, alkenyl, or hydroxy alkyl radical of from about 8 to about 18 carbon atoms, from 0 to about 10 ethylene oxide moieties and from O to 1 glyceryl moiety; Y is selected from the group consisting of nitrogen, phosphorous, and sulfur atoms; R is an alkyl or monohydroxy alkyl group containing 1 to about 3 carbon atoms; x is 1 when y is a sulfur atom and 2 when Y is a nitrogen or phosphorous atom, R is an alkylene or hydroxy alkylene of from 1 to about 4 carbon atoms and Z is a radical selected from the group consisting of carboxylate, sulfonate, sulfate, phosphonate, and phosphate groups.
Other examples include:
4- [N,N-di 2-hydroxyethyl) -N-octadecylammonio] butane-l-carboxylate;
5- [S-3-hydroxypropyl-S-hexadecyl sulfonio] -3-hydroxypentane-l-sulfate;
3- [P,P-diethyl-P-3 ,6',9-trioxatetracosylphosphonio] -2-hydroxypropanel-phosphate;
3- [N,N-dipropyl-N-3-dodecoxy-Z-hydroxypropylammonio] -propanel-phosphonate;
3 (N,N dimethyl N hexadecylammonio)propane-1- sulfonate, 3-(N,N dimethyl-N-hexadecylammonio)-2- hydroxypropane 1 sulfonate, 4-[N,N-di(2-hydroxyethyl)-N-(2 hydroxydodecyl)ammonio1-butane-1-carboxylate, 3 [S-ethyl-S-(3-dodecoxy-2-hydroxypropyl) sulfonio]-propane 1 phosphate, 3-[P,P-dimethyl-P- dodecylphosphonio]-propane 1 phosphonate, and S- [N,N-di(3-hydroxypropyl) N hexadecylammonio]2- hydroxypentane-l-sulfate.
(d) Amphoteric synthetic detergents.This group of 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, sodium 3-dodecylaminopropane sulfonate, dodecyl-beta-alamine, N-alkyltaurines such as the one prepared by reacting dodecylamine with sodium isethionate according to the teaching of US. 2,658,072, N-higher alkyl aspartic acids such as those produced according to the teaching of US. 2,438,091, and the products sold under the trade name Mirano and described in US. Pat. 2,528,378.
(2) Detergent builders The detergent builders useful in the present invention are water-soluble inorganic alkaline builder salts and organic alkaline sequestering builder salts and mixtures thereof as described and illustrated below.
Examples of water soluble inorganic alkaline builder salts (and mixtures thereof) which are used in the compositions of this invention include the sodium, potassium, ammonium and substituted ammonium salts of the alkali metal carbonates, borates, phosphates, condensed polyphosphates, bicarbonates and silicates. Specific examples of such salts are the sodium and potassium tripolyphosphates, carbonates, tetraborates, pyrophosphates, orthophosphates, bicarbonates and hexametaphosphates.
Examples of organic alkaline builder salts (and mixtures thereof) which can be used are the alkali metal, ammonium or substituted ammonium aminopolycarboxylates; for example: sodium and potassium N-(s-hydroxyethyl)-ethylenediaminetriacetates and sodium and potassium nitrilotriacetates. Other valuable polycarboxylate builders are the sodium and potassium salts of polymaleate, polyitaconate, and polyacrylate. The alkali metal salts of phytic acid are also suitable builders.
The polyphosphonates which can be used as builders for the compositions of this invention include compounds exemplified by the following: sodium and potassium salts of ethane-l-hydroxy-l, l-diphosphonate, sodium and potassium salts of methylene and ethylenediphosphonates as well as the alkali metal salts of such compounds.
Additional examples of builders useful in the present invention are disclosed by Lyness and OConnor in US. Pat. 3,336,230, said patent being incorporated herein by reference.
(3) Fluoroalkyl suds suppressing agent The fluoroalkyl compounds useful in the present invention as suds suppressing agents have the following general formula:
wherein R is selected from the group consisting of R1 m Zm n Zn O m Zm n 2n and mixtures thereof; and when y =2 one R group can be H; where m is an integer from 1 to about 12, n is an integer from 1 to about 16, the total of m-i-n equal an integer of from about 2 to about 18, y is a number of average value from 1.0 to 2.5 (The term average value is used to show that mixtures are contemplated as part of the present invention), R is selected from the group consisting of hydrogen and F, and M is selected from the group consisting of hydrogen, alkali metal, ammonium and substituted ammonium.
The fluoroalkyl suds suppressors of the present invention can be utilized alone or in combination and include both the free acid and water soluble salt forms. As used herein and in the accompanying examples fiuoroalkyl suds suppressors refers to both the acid and water soluble salt forms. Operable salts include the alkali metal (e.g., sodium and potassium), ammonium and substituted ammonium (e.g., mono-, di-, and triethanolammonium) salts. Preferred compounds of this class contain in their alkyl structure a straight chain of at least 2 carbon atoms and not less than 4 fluorine atoms. Examples of such preferred structures include the following:
wherein M is hydrogen, alkali metal, ammonium or substituted ammonium. Included in the fluoroalkyl suds suppressing agents of the present invention are compounds commercially available from E. I. du Pont de Nemours & Company under the trade name Zonyl. Additional ex amples of operable fluoroalkyl suds suppressors and methods for their preparation, are disclosed by Benning in U.S. Pat. 2,559,749 and by Brace and MacKenZie in US. Pat. 3,083,224, said patents being incorporated herein by reference.
As hereinbefore stated the fiuoroalkyl suds suppressing agents can be used in amounts ranging from about 0.1% to about 8.0% by weight of the total composition. Amounts of less than about 0.1% do not give desirable suds suppressing effects whereas amounts greater than 8% do not appear to produce any greater effect than is attainable with lesser concentrations, thus utilization of such higher amounts is uneconomical and serves no purpose. Preferably the amount is from about 1% to about 3%.
PREFERRED EMBODIMENTS A preferred embodiment of the present invention contains from about 1% to about 50% by weight of a per compound bleaching agent, such as sodium perborate. The per compound bleaching agent imparts a high level of cleaning and bleaching power to the compositions particularly when used in conjunction with the builder materials described above. Other per compounds which can be used in place of the sodium perborate or in addition thereto include compounds such as sodium percarbonate and sodium persulfate. The potassium and substituted ammonium salts can also be used. The per compounds derive their bleaching power from the release of active oxygen in solution. Sodium perborate is the preferred per compound bleaching agent. From about %to about is the preferred range of usage of the per compound bleaching agent.
A further preferred embodiment includes in the detergent part of the compositions of the present invention from about 0.5% to about 6%, preferably from about 1% to about 3% of a nonionic condensation product. The use of a nonionic condensation product aids in reducing the suds level.
The compounds are the condensation product of aliphatic alcohols having from about 12 to about 22 carbon atoms, in either a straight chain or a branched chain configuration, with ethylene oxide. A typical example is a tallow alcohol-ethylene oxide condensate having from about 5 to about 30 moles (or up to about moles) of ethylene oxide per mole of tallow alcohol. Preferred compounds include tallow alcohol-ethylene oxide condensation product containing 11 moles of ethylene oxide per mole of tallow alcohol. The term tallow as used herein and in the accompanying examples indicates a carbon chain length distribution approximately as follows: 2.5% C 28%C 23%C 2% palmitoleic, 41.5% oleic and 3% linoleic (the first three fatty acids are saturated). The term coconut (for example, in a coconut alcohol-ethylene oxide condensation product) applies to a distribution of carbon chain lengths which is approximately as follows: 8%03, 7%C10, 48%012, 17% 14! 9%C16, C 7% oleic and 2% linoleic (the first six fatty acids listed are saturated).
In formulating the compositions of this invention, it is essential that the proportion of the ingredients set forth above be observed. Within these proportions the principal object of this invention is observed, i.e., control of the sudsing level attributed in part to sudsing of the organic detergent ingredient which is aggravated by oxygen evolution from any per compound bleaching agent employed in the system.
One of the principal advantages of the present invention is that the suds control mechanism of the fluoroalkyl suds suppressor is not materially affected by the water hardness. It is well known that most prior art suds suppressor agents, such as fatty acids and fatty acid soaps lose some of their effectiveness in hard water.
An additional advantage of the present invention is the excellent whiteness maintenance that the compositions provide. Many suds suppressors are insoluble and deposit on articles washed with compositions containing them leading, to a decrease in the whiteness of the articles. The compositions of this invention containing the fluoroalkyl suds suppressing agents indicate no such deposition problems.
The ingredients of the compositions of this invention are preferably employed in the form of complete detergent formulations. These complete detergent formulations can be prepared in any of several forms including granular, flake, liquid or tablet.
The compositions can contain particulate inorganic salts which are inert to the formula to act as fillers. Examples of such salts include sodium sulfate and sodium chloride.
The compositions of the present invention can also con tain adjuvants, diluents, soil suspending agents such as carboxymethylcellulose and additives including germicidal agents, enzymes, anti-tarnishing agents, optical brightners and dyes. Such additional miscellaneous ingredients can be employed in amounts about 10% by weight of the composition.
The compositions of this invention can be prepared in any suitable manner as long as the proportions set forth herein are followed. Numerous methods are known in the art for preparing such compositions; for instance, ingredients can be mechanically admixed, spray-dried or agglomerated according to the stated proportions.
The following examples illustrates in detail the manner in which the invention can be practiced. It will be understood, however, that the invention is not confined to the specific limitations set forth in the individual examples but rather to the scope of the appended claims.
The evaluation procedure to which reference is made in the following examples is a method which was developed to determine the suds profile of low sudsing detergent formulations. These tests are conducted in four smaller than normal (about scale), specially designed, horizontally rotating drum washing machines which operate simultaneously and simulate as closely as possible the agitation, temperature control, product concentration, and water conditions of an actual tumbler type washing machine in operation. The machines are so designed (with a transparent front) that the suds heights and water temperatures can be visually observed and recorded throughout any specific test. Cloths to be tested are worn by panelists and distributed so that equal amounts of naturally soiled fabrics are washed in each machine. The load comprises two T-shirts weighing about 200 grams and nine socks weighing about 200 grams. A standard test includes two periods which differ only in temperature and concentration of the detergent compositions. The temperatures are higher and the concentrations greater in the second period. During the first washing period lasting ten minutes, the water temperature is raised from 60 F. to about F. by the heaters which are built into the machine. A portion of the wash solution is then removed from the machines and replaced by an equal quantity of hard water and a weight of detergent composition equal to the amount added for the first period. This represents the second period as referred to below and the temperature is raised to about F.
The suds levels and temperatures are recorded at least every two minutes. In this way the actual use and fall, if any, of the suds in response to the soil load, water hardness, product formulation, and increase in temperature can be observed. It takes approximately twenty minutes after the second period is begun for the water in the machines to reach 190 F. The machines are designed to be operated with about three liters of water. Soft water is adjusted to the desired hardness, about 15 grains per gallon, by the A detergent composition containing the following ingredients was prepared in the manner explained below.
Ingredients: Parts by wt. Sodium salt of tallowalkyl sulfate wherein the tallowalkyl is a mixture of chain lengths from 14 to 18 carbon atoms 5.0 Sodium tripolyphosphate 32.0 Sodium silicate solids (SiO :Na O=2:1) 7.0 Sodium sulfate 19.0 Sodium perborate tetrahydrate 25.0 Water Balance to 100 The alkyl sulfate was mixed with water to obtain a paste and a 44% water solution of sodium silicate solids was added to the paste. To this mixture was added separately in powdered form the following ingredients: sodium tripolyphosphate, sodium perborate and sodium sulfate. This resulting mixture is utilized in its paste form.
The sudsing characteristics of this composition were determined in the laundry screening test as described above. Temperature and suds heights were taken at two minute intervals during the second period and the results recorded. In conducting the test, 18 grams of the above composition were added to three liters of water containing about 400 grams of naturally soiled cloths. A ten minute first period was followed by replacement of 1.2 liters of the solution with an equal amount of clean hard water and an additional 18 grams of the detergent composition. Heat and agitation were supplied for a second period of 40 minutes. The hardness of the water was adjusted to gr./liter by the addition of calcium chloride.
A similar test was simultaneously run utilizing the same basic detergent composition and testing conditions except that 2.0% by Weight of wherein n is an average of 7, x is an average of 1.5 and y=3x was added to the composition. The term average indicates that a mixture of suds suppressing agents was utilized. This suds suppressing mixture was added to the powdered ingredients of the basic detergent composition in a methanol solution and the methanol allowed to evaporate completely before the testing began.
Table 1 below shows the elfect of the suds suppressing agents of the present invention. (In Table I and subsequent tables, the suds heights are reported at equal temperature intervals rather than the two minute intervals at which they were recorded to permit a more direct comparison of the results.)
Table I shows the suds suppressing effect of the detergent compositions containing the suds suppressing agents over the detergent compositions that do not contain these agents.
When 2% by weight of H(CF CH O-PO(OH) was substituted for the suds suppressing agent mixture of Example I the following results were obtained.
These results of the suds suppressing effect are summarized in Table II. This effect is noticed particularly above 160 P. where oxygen is released by the perborate bleaching agent.
TABLE II Suds height in centimeters Suds suppress- Basic detergent composition with No additive ing agent Degrees F.:
Table II clearly shows the advantageous effect of the detergent compositions containing the suds suppressing agents.
When about 3.0% by weight of a nonion'ic condensation product, e.g., tallow alcohol-ethylene oxide condensation product containing an average of 11 moles of ethylene oxide, is added with the fiuoroalkyl suds suppressing agents of the present invention to the composition of Example I a further reduction in suds height is noted.
Substantially the same suds suppressing results, i.e., low to medium sudsing, are obtained with the compositions of Example I containing the fiuoroalkyl suds suppressing agent when any of the following detergents are P substituted on an equal weight basis for the sodium salt of tallow alkyl sulfate in Example 1:
Substantially the same results are obtained with the compositions of Example I, i.e., low to medium sudsing and good cleaning when the sodium perborate tetrahydrate is replaced on an equal weight basis by sodium percarbonate or sodium persulfate.
EXAMPLE II The detergent composition set forth below was prepared in the manner described in Example I and the sudsing characteristics evaluated by the same laundry screening test.
Ingredients: Parts by wt. Sodium salt of linear alkylbenzene sulfonate having an average chain length of 11.8 9.0 Sodium tripolyphosphate 32.0 Sodium silicate solids (SiO :Na O=2:l) 7.0 Sodium sulfate 19.0 Sodium perborate tetrahydrate 25.0 Water Balance to 100 TABLE III Suds height in centimeters Suds suppress- Basie detergent composition with N0 additive ing agent Degrees F.:
The suds suppressing agent utilized was H (CF CH -OPO (OH 2 when H (CF 7CH2 OPO (OH) 2 are substituted on an equal weight basis for the fluoroalkyl suds suppressing agent of Example II substantially equivalent suds suppressing results are obtained.
Substantially equivalent results, i.e., low to medium sudsing with good cleaning, are obtained when the sodium salt of linear alkylbenzene sulfonate having an average chain length of 11.8 is replaced on an equal weight basis in the compositions of Example II by:
condensation product of octyl phenol with moles of ethylene oxide per mole of octyl phenol;
dimethylhexadecylamine oxide;
dimethyldodecylamine oxide;
dodecyldimethylphosphine oxide;
3,6,9-trioxaoctadecyldimethylphosphine oxide;
dodecyl methyl sulfoxide; or
B-hydroxytridecyl methyl sulfoxide.
EXAMPLE. III
The detergent composition described below was prepared in the manner described in Example I.
Ingredients: Parts by wt. Coconut alcohol-ethylene oxide condensation product containing 6 moles of ethylene oxide 8.0 Sodium tripolyphosphate 32.0 Sodium silicate solids (SiO :Na O=2:1) 7.0 Sodium sulfate 19.0 Sodium perborate tetrahydrate 25.0 Water Balance to 100 The sudsing characteristics of this composition were compared to that of identical compositions containing 2.0% by weight of a suds suppressing agent of the formula The comparisons were run in the laundry screening test previously described with the results given in Table IV. These results show a definite suds suppressing effect with the fluoroalkyl suds suppressing agent of the present invention.
The detergent composition described below was prepared in the manner described in Example I.
Ingredients: Parts by wt.
3 (N,N dimethyl-N-hexadecylammonio)-2- hydroxypropane-l-sulfonate 4.0 Sodium tripolyphosphate 32.0 Sodium silicate solids (SiO :Na O=2:1) 7.0 Sodium sulfate 19.0 Sodium perborate tetrahydrate 25.0 Water Balance to 100 The sudsing characteristics of this composition were compared to that of identical compositions containing 2% by weight of a suds suppressing agent of the formula H (CF CH OPO (OH) 2 The comparisons were run in the laundry screening test previously described and the results in Table V below show the suds suppressing eifect of the fluoroalkyl suds suppressing agent of the present invention.
TABLE V Suds height in centimeters Suds suppress- Basic detergent composition with No additive iug agent Degrees F.:
Substantially equivalent results are obtained, i.e., low to medium sudsing and good cleaning, when the 3-(N,N- dimethyl-N-hexadecylammonio) 2 hydroxypropane-lsulfonate of Example IV is replaced by:
3- N,N-dimethyl-N-hexadecylamm onio -2-propanel-sulfonate;
3-[P, P-dimethyl-P-dodecylphosphonio1 propane 1 phosphonate;
3-dodecylaminopropionate; or
dodecyl-beta-alanine.
EXAMPLE V The following detergent composition was prepared:
Ingredients: Parts by wt.
Sodium tallow-sodium coconut soap (tallow:
coconut=4:1) 6.0 Sodium tripolyphosphate 32.0 Sodium silicate solids (SiO :Na O=2:1) 7.0 Sodium sulfate 19.0 Sodium perborate tetrahydrate 25.0
Water Balance to 100 The sudsing characteristics of this composition were compared to that of an identical composition containing 2% by weight of a suds suppressing agent of the formula The comparisons were run in the laundry screening test previously described and the results in Table VI below show the suds suppressing effect of the suds suppressing agents of the present invention.
TABLE VI Suds height in centimeters Suds supprcssing agent Basic detergent composition with No additive The advantages of the present invention, while capable of demonstration with all of the aforementioned detergents, are especially notable with high sudsing detergents which provide exceptionally high levels of cleaning.
A special embodiment of the present invention comprises the use of a non-soap synthetic detergent as the detergent component of the composition.
In addition to the preferred embodiments described herein, other arrangements and variations within the spirit and scope of the invention and the appended claims will occur to those skilled in the art.
What is claimed is:
1. A low to medium-sudsing laundry detergent composition consisting essentially of, by Weight, from about 2% to about 30% of a detergent selected from the group consisting of alkali metal soaps; anionic, non-soap synthetic detergents; nonionic, non-soap synthetic detergents; zwitterionic, non-soap synthetic detergents and amphoteric, non-soap synthetic detergents; from about 2% to about 65% of a detergent builder selected from the group consisting of water-soluble inorganic alkaline builder salts, organic alkaline sequestering builder salts and mixtures thereof; and from about 0.1% to about 8% of a fluoroalkyl suds suppressing agent of the general formula wherein R is selected from the group consisting of 3. The composition of claim 2 wherein the fluoroalkyl suds suppressing agent is H'(CF CH -OPO (OH) 2 4. The composition of claim 2 wherein the fluoroalkyl suds suppressing agent is wherein n is an average of 7, x is an average of 1.5 and y=3-x.
5. The composition of claim 1 wherein the non-soap 1 1- synthetic detergent is the sodium salt of an alkyl sulfate wherein the alkyl group contains from about 8 to about 18 carbon atoms and mixtures thereof.
6. The composition of claim 1 wherein the non-soap synthetic detergent is the sodium salt of a random paraffin sulfonate containing an average of from about 10 to about 20 carbon atoms.
7. The composition of claim 1 wherein the detergent is a mixture of tallow and coconut soaps in a ratio of about 4:1.
8. The composition of claim 1 containing from about 1% to about 50% by weight of a per compound bleaching agent selected from the group consisting of sodium perborate, sodium percarbonate, sodium persulfate, potassum perborate, potassium percarbonate, potassium persulfate, substituted ammonium perborate, substituted ammonium percarbonate and substituted ammonium persulfate.
9. The composition of claim 10 wherein the per compound bleaching agent is sodium perborate and the builder is sodium tripolyphosphate.
10. The composition of claim 1 wherein the detergent is a mixture of detergents containing from about 0.5% to about 6% by weight of the nonionic condensation product of alcohols having from 8 to 18 carbon atoms with 1030 moles of ethylene oxide.
References Cited UNITED STATES PATENTS 6/1967 lnamorato 202-137 11/1968 Gotte et a1. 20299 UNITED STATES PATENT OFFICE CERTIFICATE OF CORRECTION Patent No. 3, 585, l 45 Dated J ge 15, 19 71 Inventor) Walter P. Fethke, Jr.
It is certified that error appears in the above-identified patent and that said Letters Patent are hereby corrected as shown below:
Column 1, ine 23, "fluoralkyl" should read fluoroalkyl Column 6, line 45, 'where" should read wherein Column 8, line 33, "illustrates" should read illustrate Column 10, line 15, 13.0" should read'- l0.0-;
line 17, "9.3" should read 9.0 line 18, "30.5" should read 10.5 line 19, "380" should read 180 Signed and sealed this 21st day of December 1971.
(SEAL) Attest:
EDWARD M.FLETCHER,J'R. ROBERT GOTTSCHALK Attesting Officer Acting Commissioner of Patents
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US74627468A | 1968-07-22 | 1968-07-22 |
Publications (1)
Publication Number | Publication Date |
---|---|
US3585145A true US3585145A (en) | 1971-06-15 |
Family
ID=25000147
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US746274A Expired - Lifetime US3585145A (en) | 1968-07-22 | 1968-07-22 | Low sudsing detergent compositions |
Country Status (11)
Country | Link |
---|---|
US (1) | US3585145A (en) |
AT (1) | AT310907B (en) |
BE (1) | BE736280A (en) |
CH (1) | CH510734A (en) |
DE (1) | DE1936843C3 (en) |
ES (1) | ES369740A1 (en) |
FR (1) | FR2014675A1 (en) |
GB (1) | GB1269378A (en) |
NL (2) | NL160329C (en) |
NO (1) | NO130594C (en) |
SE (1) | SE353545B (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3910886A (en) * | 1969-07-18 | 1975-10-07 | Us Agriculture | Organo-phosphorus compounds containing perfluoroalkyl radicals and aziridine radicals |
US3948819A (en) * | 1970-05-20 | 1976-04-06 | Minnesota Mining And Manufacturing Company | Cleaning composition |
FR2387648A1 (en) * | 1977-04-18 | 1978-11-17 | Unilever Nv | SHAMPOO WITH ANTI-GREASE PROPERTIES |
US4176176A (en) * | 1974-05-31 | 1979-11-27 | Alberto-Culver Company | Hair shampoo and cleanser compositions |
US4183367A (en) * | 1976-06-17 | 1980-01-15 | American Cyanamid Company | Enhancing the drying of hair by the use of fluorinated catonic and amphoteric surfactants |
DE3236114A1 (en) * | 1981-10-01 | 1983-04-14 | Niels Ole 8520 Lystrup Vesterager | WASHING ACTIVE DOSING UNIT, METHOD FOR THE PRODUCTION THEREOF AND USE THEREOF |
US6258772B1 (en) * | 1999-10-12 | 2001-07-10 | Bay Technologies, Inc. | Cleaning compositions comprising perfluorinated alkylphosphates |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2233941C3 (en) * | 1972-07-11 | 1978-03-02 | Cassella Farbwerke Mainkur Ag, 6000 Frankfurt | Use of perfluoroalkylphosphorus compounds as foam suppressants |
DE3723198A1 (en) * | 1987-07-14 | 1989-02-16 | Bayer Ag | FOAM-RESISTANT ADDITIVE IN ACID SOURS AND GALVANIC BATHS |
-
0
- NL NL130594D patent/NL130594C/xx active
-
1968
- 1968-07-22 US US746274A patent/US3585145A/en not_active Expired - Lifetime
-
1969
- 1969-07-17 FR FR6924418A patent/FR2014675A1/fr not_active Withdrawn
- 1969-07-18 BE BE736280D patent/BE736280A/xx unknown
- 1969-07-18 NO NO2997/69A patent/NO130594C/no unknown
- 1969-07-19 DE DE1936843A patent/DE1936843C3/en not_active Expired
- 1969-07-21 CH CH1114669A patent/CH510734A/en not_active IP Right Cessation
- 1969-07-21 SE SE10256/69A patent/SE353545B/xx unknown
- 1969-07-22 GB GB36728/69A patent/GB1269378A/en not_active Expired
- 1969-07-22 ES ES369740A patent/ES369740A1/en not_active Expired
- 1969-07-22 AT AT704569A patent/AT310907B/en not_active IP Right Cessation
- 1969-07-22 NL NL6911186.A patent/NL160329C/en active
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3910886A (en) * | 1969-07-18 | 1975-10-07 | Us Agriculture | Organo-phosphorus compounds containing perfluoroalkyl radicals and aziridine radicals |
US3948819A (en) * | 1970-05-20 | 1976-04-06 | Minnesota Mining And Manufacturing Company | Cleaning composition |
US4176176A (en) * | 1974-05-31 | 1979-11-27 | Alberto-Culver Company | Hair shampoo and cleanser compositions |
US4183367A (en) * | 1976-06-17 | 1980-01-15 | American Cyanamid Company | Enhancing the drying of hair by the use of fluorinated catonic and amphoteric surfactants |
FR2387648A1 (en) * | 1977-04-18 | 1978-11-17 | Unilever Nv | SHAMPOO WITH ANTI-GREASE PROPERTIES |
DE3236114A1 (en) * | 1981-10-01 | 1983-04-14 | Niels Ole 8520 Lystrup Vesterager | WASHING ACTIVE DOSING UNIT, METHOD FOR THE PRODUCTION THEREOF AND USE THEREOF |
US6258772B1 (en) * | 1999-10-12 | 2001-07-10 | Bay Technologies, Inc. | Cleaning compositions comprising perfluorinated alkylphosphates |
Also Published As
Publication number | Publication date |
---|---|
DE1936843A1 (en) | 1970-01-22 |
NL160329B (en) | 1979-05-15 |
NL160329C (en) | 1979-10-15 |
NL130594C (en) | |
BE736280A (en) | 1970-01-19 |
CH510734A (en) | 1971-07-31 |
FR2014675A1 (en) | 1970-04-17 |
DE1936843C3 (en) | 1979-01-18 |
NL6911186A (en) | 1970-01-26 |
GB1269378A (en) | 1972-04-06 |
DE1936843B2 (en) | 1978-05-11 |
SE353545B (en) | 1973-02-05 |
ES369740A1 (en) | 1971-06-16 |
AT310907B (en) | 1973-10-25 |
NO130594B (en) | 1974-09-30 |
NO130594C (en) | 1975-01-08 |
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