USRE37555E1 - Process and composition for multicomponent one hundred percent solid fabric softeners - Google Patents
Process and composition for multicomponent one hundred percent solid fabric softeners Download PDFInfo
- Publication number
- USRE37555E1 USRE37555E1 US09/330,621 US33062199A USRE37555E US RE37555 E1 USRE37555 E1 US RE37555E1 US 33062199 A US33062199 A US 33062199A US RE37555 E USRE37555 E US RE37555E
- Authority
- US
- United States
- Prior art keywords
- fatty acid
- quaternary ammonium
- tertiary amine
- ammonium compound
- carbon atoms
- 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 claims abstract description 62
- 238000000034 method Methods 0.000 title claims abstract description 18
- 239000002979 fabric softener Substances 0.000 title abstract description 6
- 239000007787 solid Substances 0.000 title description 4
- 150000003856 quaternary ammonium compounds Chemical class 0.000 claims abstract description 61
- 235000014113 dietary fatty acids Nutrition 0.000 claims abstract description 52
- 239000000194 fatty acid Substances 0.000 claims abstract description 52
- 229930195729 fatty acid Natural products 0.000 claims abstract description 52
- -1 fatty acid ester Chemical class 0.000 claims abstract description 52
- 150000004665 fatty acids Chemical class 0.000 claims abstract description 33
- 239000002904 solvent Substances 0.000 claims abstract description 17
- 150000001875 compounds Chemical class 0.000 claims abstract description 7
- 125000000217 alkyl group Chemical group 0.000 claims description 31
- 125000004432 carbon atom Chemical group C* 0.000 claims description 30
- 239000004744 fabric Substances 0.000 claims description 26
- 229920006395 saturated elastomer Polymers 0.000 claims description 22
- 150000003512 tertiary amines Chemical class 0.000 claims description 17
- 125000001183 hydrocarbyl group Chemical group 0.000 claims description 16
- 239000003795 chemical substances by application Substances 0.000 claims description 15
- 229930195734 saturated hydrocarbon Natural products 0.000 claims description 14
- 125000001931 aliphatic group Chemical group 0.000 claims description 13
- 239000003599 detergent Substances 0.000 claims description 12
- 229930195735 unsaturated hydrocarbon Natural products 0.000 claims description 12
- 239000000758 substrate Substances 0.000 claims description 10
- 150000001412 amines Chemical group 0.000 claims description 8
- 150000001450 anions Chemical class 0.000 claims description 8
- 239000001257 hydrogen Substances 0.000 claims description 8
- 229910052739 hydrogen Inorganic materials 0.000 claims description 8
- 125000002947 alkylene group Chemical group 0.000 claims description 7
- 238000004519 manufacturing process Methods 0.000 claims description 7
- 150000002148 esters Chemical class 0.000 claims description 6
- MTNDZQHUAFNZQY-UHFFFAOYSA-N imidazoline Chemical compound C1CN=CN1 MTNDZQHUAFNZQY-UHFFFAOYSA-N 0.000 claims description 6
- 150000003839 salts Chemical class 0.000 claims description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 5
- 150000004670 unsaturated fatty acids Chemical class 0.000 claims description 5
- 235000021122 unsaturated fatty acids Nutrition 0.000 claims description 5
- 125000003545 alkoxy group Chemical group 0.000 claims description 4
- 125000003342 alkenyl group Chemical group 0.000 claims description 3
- 229910052757 nitrogen Inorganic materials 0.000 claims description 3
- 239000000271 synthetic detergent Substances 0.000 claims description 3
- 238000004140 cleaning Methods 0.000 claims description 2
- 239000000463 material Substances 0.000 claims description 2
- 239000000344 soap Substances 0.000 claims description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 4
- 150000004671 saturated fatty acids Chemical class 0.000 claims 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 3
- 125000005526 alkyl sulfate group Chemical group 0.000 claims 2
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 2
- 238000006243 chemical reaction Methods 0.000 abstract description 14
- 238000002156 mixing Methods 0.000 abstract description 5
- 239000000645 desinfectant Substances 0.000 abstract description 2
- 238000011065 in-situ storage Methods 0.000 abstract description 2
- 238000005956 quaternization reaction Methods 0.000 abstract description 2
- 239000003760 tallow Substances 0.000 description 10
- 0 *N(C)C Chemical compound *N(C)C 0.000 description 9
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 6
- 239000006260 foam Substances 0.000 description 5
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical class [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 4
- KXKVLQRXCPHEJC-UHFFFAOYSA-N COC(C)=O Chemical compound COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 4
- 235000019270 ammonium chloride Nutrition 0.000 description 4
- 230000000844 anti-bacterial effect Effects 0.000 description 4
- PMDCZENCAXMSOU-UHFFFAOYSA-N CCNC(C)=O Chemical compound CCNC(C)=O PMDCZENCAXMSOU-UHFFFAOYSA-N 0.000 description 3
- 239000003899 bactericide agent Substances 0.000 description 3
- VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 description 3
- 238000005553 drilling Methods 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 239000003129 oil well Substances 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- KUVIBAJMTUGZMU-UHFFFAOYSA-N CC(=O)NCN1CCN=C1C Chemical compound CC(=O)NCN1CCN=C1C KUVIBAJMTUGZMU-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- MTKLMICCDVAPTK-UHFFFAOYSA-I I[V](I)I.I[V]I.[H]C(C)(C)CNC(C)=O.[H]C1(C)C(C)=NC(C)(C)C1(C)C Chemical compound I[V](I)I.I[V]I.[H]C(C)(C)CNC(C)=O.[H]C1(C)C(C)=NC(C)(C)C1(C)C MTKLMICCDVAPTK-UHFFFAOYSA-I 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 2
- 229920005830 Polyurethane Foam Polymers 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-L adipate(2-) Chemical compound [O-]C(=O)CCCCC([O-])=O WNLRTRBMVRJNCN-UHFFFAOYSA-L 0.000 description 2
- 150000003863 ammonium salts Chemical class 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- KCXMKQUNVWSEMD-UHFFFAOYSA-N benzyl chloride Chemical compound ClCC1=CC=CC=C1 KCXMKQUNVWSEMD-UHFFFAOYSA-N 0.000 description 2
- 229940073608 benzyl chloride Drugs 0.000 description 2
- XKXHCNPAFAXVRZ-UHFFFAOYSA-N benzylazanium;chloride Chemical compound [Cl-].[NH3+]CC1=CC=CC=C1 XKXHCNPAFAXVRZ-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- GZUXJHMPEANEGY-UHFFFAOYSA-N bromomethane Chemical compound BrC GZUXJHMPEANEGY-UHFFFAOYSA-N 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 239000002537 cosmetic Substances 0.000 description 2
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000005755 formation reaction Methods 0.000 description 2
- 150000002462 imidazolines Chemical class 0.000 description 2
- 239000000314 lubricant Substances 0.000 description 2
- 239000004745 nonwoven fabric Substances 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical class CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- 235000019198 oils Nutrition 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 2
- 239000010452 phosphate Substances 0.000 description 2
- 239000011496 polyurethane foam Substances 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 241001148471 unidentified anaerobic bacterium Species 0.000 description 2
- 235000015112 vegetable and seed oil Nutrition 0.000 description 2
- LMBGSBKIQQYYFS-UHFFFAOYSA-N 1,1,18,18,18-pentaethoxyoctadecylazanium;chloride Chemical compound [Cl-].CCOC([NH3+])(OCC)CCCCCCCCCCCCCCCCC(OCC)(OCC)OCC LMBGSBKIQQYYFS-UHFFFAOYSA-N 0.000 description 1
- QLAJNZSPVITUCQ-UHFFFAOYSA-N 1,3,2-dioxathietane 2,2-dioxide Chemical compound O=S1(=O)OCO1 QLAJNZSPVITUCQ-UHFFFAOYSA-N 0.000 description 1
- GOHZKUSWWGUUNR-UHFFFAOYSA-N 2-(4,5-dihydroimidazol-1-yl)ethanol Chemical compound OCCN1CCN=C1 GOHZKUSWWGUUNR-UHFFFAOYSA-N 0.000 description 1
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical class [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- 241000894006 Bacteria Species 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- JSJARQHQJPNMDQ-UHFFFAOYSA-N C.C.CC(=O)NCN(C)C.CC(=O)NCN(C)C Chemical compound C.C.CC(=O)NCN(C)C.CC(=O)NCN(C)C JSJARQHQJPNMDQ-UHFFFAOYSA-N 0.000 description 1
- LPJJMICYUSEOGZ-UHFFFAOYSA-M C.CC(=O)NCC(C)(C)C.CC(=O)NCC(C)C.CC1=NC(C)(C)C(C)(C)C1(C)C.[V]I Chemical compound C.CC(=O)NCC(C)(C)C.CC(=O)NCC(C)C.CC1=NC(C)(C)C(C)(C)C1(C)C.[V]I LPJJMICYUSEOGZ-UHFFFAOYSA-M 0.000 description 1
- TZBQXPMXRZGBCY-UHFFFAOYSA-N C.CC1=NC(C)(C)C(C)(C)C1(C)C Chemical compound C.CC1=NC(C)(C)C(C)(C)C1(C)C TZBQXPMXRZGBCY-UHFFFAOYSA-N 0.000 description 1
- JCCVVUYNOCEALA-UHFFFAOYSA-N CC(=O)NCN(C)C Chemical compound CC(=O)NCN(C)C JCCVVUYNOCEALA-UHFFFAOYSA-N 0.000 description 1
- FILXDXZGAFFZLQ-UHFFFAOYSA-N CC(=O)NCN(C)CN1C(C)=NC(C)(C)C1(C)C Chemical compound CC(=O)NCN(C)CN1C(C)=NC(C)(C)C1(C)C FILXDXZGAFFZLQ-UHFFFAOYSA-N 0.000 description 1
- VUOUOCLMOPUMNH-UHFFFAOYSA-N CC1=NC(C)(C)C(C)(C)C1(C)C Chemical compound CC1=NC(C)(C)C(C)(C)C1(C)C VUOUOCLMOPUMNH-UHFFFAOYSA-N 0.000 description 1
- CDTWIBZYMDXUEU-UHFFFAOYSA-N CC1=NC(C)(C)C(C)(C)N1C Chemical compound CC1=NC(C)(C)C(C)(C)N1C CDTWIBZYMDXUEU-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 description 1
- 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 1
- 241001465754 Metazoa Species 0.000 description 1
- 238000005481 NMR spectroscopy Methods 0.000 description 1
- IOVCWXUNBOPUCH-UHFFFAOYSA-M Nitrite anion Chemical compound [O-]N=O IOVCWXUNBOPUCH-UHFFFAOYSA-M 0.000 description 1
- 229920001944 Plastisol Polymers 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids 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
- 125000005233 alkylalcohol group Chemical group 0.000 description 1
- 235000011114 ammonium hydroxide Nutrition 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- NUKAPDHENUQUOI-UHFFFAOYSA-N benzyl(18-methylnonadecyl)azanium;chloride Chemical compound [Cl-].CC(C)CCCCCCCCCCCCCCCCC[NH2+]CC1=CC=CC=C1 NUKAPDHENUQUOI-UHFFFAOYSA-N 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical group OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 230000001680 brushing effect Effects 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- NEHMKBQYUWJMIP-NJFSPNSNSA-N chloro(114C)methane Chemical compound [14CH3]Cl NEHMKBQYUWJMIP-NJFSPNSNSA-N 0.000 description 1
- 235000019864 coconut oil Nutrition 0.000 description 1
- 239000003240 coconut oil Substances 0.000 description 1
- 229940125844 compound 46 Drugs 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 125000004210 cyclohexylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
- DENRZWYUOJLTMF-UHFFFAOYSA-N diethyl sulfate Chemical compound CCOS(=O)(=O)OCC DENRZWYUOJLTMF-UHFFFAOYSA-N 0.000 description 1
- 229940008406 diethyl sulfate Drugs 0.000 description 1
- POCFBDFTJMJWLG-UHFFFAOYSA-N dihydrosinapic acid methyl ester Natural products COC(=O)CCC1=CC(OC)=C(O)C(OC)=C1 POCFBDFTJMJWLG-UHFFFAOYSA-N 0.000 description 1
- IUNMPGNGSSIWFP-UHFFFAOYSA-N dimethylaminopropylamine Chemical compound CN(C)CCCN IUNMPGNGSSIWFP-UHFFFAOYSA-N 0.000 description 1
- SMVRDGHCVNAOIN-UHFFFAOYSA-L disodium;1-dodecoxydodecane;sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O.CCCCCCCCCCCCOCCCCCCCCCCCC SMVRDGHCVNAOIN-UHFFFAOYSA-L 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 235000019197 fats Nutrition 0.000 description 1
- 150000002194 fatty esters Chemical class 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 229940013317 fish oils Drugs 0.000 description 1
- 239000004519 grease Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 1
- 239000000976 ink Substances 0.000 description 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 238000004900 laundering Methods 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- 239000002932 luster Substances 0.000 description 1
- 229940102396 methyl bromide Drugs 0.000 description 1
- 150000004702 methyl esters Chemical class 0.000 description 1
- JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical compound COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 description 1
- 150000005451 methyl sulfates Chemical class 0.000 description 1
- VIMIOFRPJXGJGK-UHFFFAOYSA-N methylazanium;octadecanoate Chemical compound NC.CCCCCCCCCCCCCCCCCC(O)=O VIMIOFRPJXGJGK-UHFFFAOYSA-N 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 125000004923 naphthylmethyl group Chemical group C1(=CC=CC2=CC=CC=C12)C* 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 229940112041 peripherally acting muscle relaxants other quaternary ammonium compound in atc Drugs 0.000 description 1
- 239000004999 plastisol Substances 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 235000011118 potassium hydroxide Nutrition 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 239000011253 protective coating Substances 0.000 description 1
- 238000010926 purge Methods 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011369 resultant mixture Substances 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- RJSZFSOFYVMDIC-UHFFFAOYSA-N tert-butyl n,n-dimethylcarbamate Chemical compound CN(C)C(=O)OC(C)(C)C RJSZFSOFYVMDIC-UHFFFAOYSA-N 0.000 description 1
- 239000013008 thixotropic agent Substances 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 125000005023 xylyl group Chemical group 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
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/04—Detergent materials or soaps characterised by their shape or physical properties combined with or containing other objects
- C11D17/041—Compositions releasably affixed on a substrate or incorporated into a dispensing means
- C11D17/042—Water soluble or water disintegrable containers or substrates containing cleaning compositions or additives for cleaning compositions
- C11D17/044—Solid compositions
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/36—Carboxylic acids; Salts or anhydrides thereof
- A61K8/361—Carboxylic acids having more than seven carbon atoms in an unbroken chain; Salts or anhydrides thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/37—Esters of carboxylic acids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/41—Amines
- A61K8/416—Quaternary ammonium compounds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/12—Preparations containing hair conditioners
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C211/00—Compounds containing amino groups bound to a carbon skeleton
- C07C211/62—Quaternary ammonium compounds
- C07C211/63—Quaternary ammonium compounds having quaternised nitrogen atoms bound to acyclic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/86—Mixtures of anionic, cationic, and non-ionic compounds
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D11/00—Special methods for preparing compositions containing mixtures of detergents
-
- 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
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/04—Detergent materials or soaps characterised by their shape or physical properties combined with or containing other objects
- C11D17/041—Compositions releasably affixed on a substrate or incorporated into a dispensing means
-
- 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
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/04—Detergent materials or soaps characterised by their shape or physical properties combined with or containing other objects
- C11D17/041—Compositions releasably affixed on a substrate or incorporated into a dispensing means
- C11D17/046—Insoluble free body dispenser
-
- 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
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/04—Detergent materials or soaps characterised by their shape or physical properties combined with or containing other objects
- C11D17/041—Compositions releasably affixed on a substrate or incorporated into a dispensing means
- C11D17/047—Arrangements specially adapted for dry cleaning or laundry dryer related applications
-
- 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
- C11D3/001—Softening 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/04—Carboxylic acids or salts thereof
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/38—Cationic compounds
- C11D1/40—Monoamines or polyamines; Salts thereof
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/38—Cationic compounds
- C11D1/42—Amino alcohols or amino ethers
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/38—Cationic compounds
- C11D1/52—Carboxylic amides, alkylolamides or imides or their condensation products with alkylene oxides
- C11D1/528—Carboxylic amides (R1-CO-NR2R3), where at least one of the chains R1, R2 or R3 is interrupted by a functional group, e.g. a -NH-, -NR-, -CO-, or -CON- group
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/38—Cationic compounds
- C11D1/58—Heterocyclic compounds
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/38—Cationic compounds
- C11D1/62—Quaternary ammonium compounds
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/667—Neutral esters, e.g. sorbitan esters
Definitions
- the invention relates to a method of producing a mixture of a quaternary ammonium compound, fatty acid, fatty acid ester and tertiary amine salt in situ which is a highly functional mixture that is manufactured in a single step reaction whereby quaternization is completed without the aid of solvents, especially flammable solvents.
- the single step reaction process eliminates separate blending of individual components.
- quaternary ammonium compounds are usually conducted in stainless steel or glass-lined equipment to which a tertiary amine is charged and a solvent.
- Flammable solvents such as isopropyl alcohol are generally used although mixtures of isopropyl alcohol and water sometimes are employed or water alone is used. Flammable solvents are also undesirable because they are a fire hazard and special handling procedures are required when they are used. In many applications, these solvents have to be stripped from the mixture when the reaction is completed because the ultimate use of the product is in a solventless or solid form.
- the reactants are loaded into the reactor they are heated to a temperature of about 50 to about 100° C. after which a quaternizing reagent is added.
- a quaternizing reagent is added.
- an exotherm is produced as a result of the quaternizing reaction and the reactor and its contents have to be cooled.
- the rate of addition of the quaternizing agent can also be controlled in order to minimize or eliminate the exotherm.
- the solvent, if any is employed in the quaternizing reaction is stripped from the quaternary ammonium compound obtained since some commercial uses for the compounds are in solventless systems. Additionally, bulk shipments of quaternary ammonium compounds with solvents adds to transportion costs which is another reason to remove the solvents.
- quaternary ammonium compounds The largest use for quaternary ammonium compounds is as a fabric softener and presently accounts for more than about three quarters of the total market for these material. Some fabric softeners are supplied as a liquid dispersion of from about 3% to about 10% by weight of the quaternary ammonium compound which is adapted to be added during the rinse cycle of a commercial or home laundering operation. Another significant fabric softening application is the utilization of quaternary ammonium compounds in combination with a substrate such as a nonwoven fabric or a polymeric foam such as a polyurethane foam, this substrate so treated being added to a fabric dryer such as a clothes dryer while the fabric or clothes are still damp.
- the quaternary ammonium compound is formulated usually with a fatty acid ester which promotes the transfer of the quaternary ammonium compound from the nonwoven or porous polymeric substrate to the fabric or clothes.
- quaternary ammonium compounds are now being added to both solid and liquid laundry detergent compositions so that the quaternary ammonium compound can be incorporated as a fabric softener during the wash cycle of fabrics or clothes.
- the most successfully utilized quaternary ammonium compounds in this last respect are the dimethyl (dihydrogenated tallow) ammonium chlorides or methyl sulfates.
- Other quaternary ammonium compounds such as imidazolines and amidoamine quaternaries are also used in this regard.
- the quaternary ammonium compound is used on a substrate for transfer to fabric or clothing in a fabric or clothes dryer, it has generally been the practice to separately blend the fatty acid ester into the quaternary ammonium compound which involves the extra manufacturing steps of transportion, handling and blending of the fatty acid esters into the quaternary ammonium compounds. If these steps can be eliminated a cost savings could be realized.
- Quaternary ammonium compounds are also used to manufacture organomodified clays which may be added to drilling muds utilized in drilling oil wells, the organomodified clay providing improved lubrication and rheological properties of the drilling muds.
- organoclays are also employed as thixotropic agents in plastisols, organosols, paints and other protective coatings, grease additives, foundry additives, cosmetics, resins and printing inks.
- the most common quaternary ammonium compounds employed in this regard are methyldi(hydrogenated tallow) benzylammonium chloride, dimethyldi(hydrogenated tallow) ammonium chloride and dimethyl(hydrogenated tallow) benzylammonium chloride.
- Quaternary ammonium compounds are also employed as bactericides the most common of which is the quaternary ammonium compound of benzylchloride and a dimethylalkylamine, the alkyl group having from about 12 to about 16 carbon atoms as well as trimethyl alkyl ammonium chlorides where the alkyl group is a long chain alkyl such as an octadecyl group. Additionally, dimethyldicoconut-oil fatty ammonium chlorides are also effective disinfectants e.g.
- bactericides or bacteristats especially against anaerobic bacteria which are sulfate reducers that are found in oil wells, these bacteria causing severe corrosion problems and plugging of formations which this type of quaternary ammonium compound can minimize or eliminate. Additionally, these quaternary ammonium compounds effective against anaerobic bacteria are also effective in removing oil from sand stone formations in oil wells and provide a two-fold effect or functioning not only as a bactericide but also in promoting so-called secondary recovery of oil.
- quaternary compounds are trimethylalkylammonium chloride, pentaethoxystearylammonium chloride, dimethylstearylbenzylammonium chloride and dimethyldialkylammonium chlorides.
- the advantage of the method of the present invention is that it provides a composition that is non-flammable and it is ready to be flaked or powdered because of its bulk form and can be used as a fabric softener, a fabric lubricant, a hair condition as well as an anti-static agent that can be released from a substrate such as a nonwoven fabric or a polymeric foam.
- These mixtures can also be used in combination with synthetic detergents or as lubricant, an emulsifier, in cosmetic preparations hair conditioning components clay modifiers, bactericidal compositions and as a floculant.
- the invention relates to a method for producing a quaternary ammonium mixture that is highly functional by means of a single step reaction as well as the various compositions that can be obtained thereby and therewith.
- the invention is directed to a method of producing a mixture of a quaternary ammonium compound, fatty acid, fatty acid ester and tertiary amine salt by reacting a tertiary amine, quaternizing agent and fatty acid, each in amount so that said mixture will contain at least a quaternary ammonium compound, a fatty acid, fatty acid ester and a tertiary amine salt.
- the tertiary amine employed according to the invention has the formula:
- R, R 1 and R 2 can be any of the following in any combination.
- R 4 is lower alkylene and R 3 is any of R, R 1 or R 2 ;
- said tertiary amine is an imidazoline of the formula:
- R 5 is a linear or branched chain, aliphatic saturated or unsaturated hydrocarbon group having up to about 22 carbon atoms and R 6 is a lower alkylene group;
- said quaternizing agent being known in the art and which will produce a quaternary ammonium compound having an anion A ⁇ .
- these quaternizing agents are those having the formula R 7 (a ⁇ b) X ;
- R 7 is a lower alkyl group or cyclo lower alkyl group such as benzyl, cyclohexylmethyl, tolyl, xylyl, naphthylmethyl
- X may be a chlorine, iodine, bromine, sulfate, methyl sulfate, carbonate, phosphate, borate group, formate, acetate, propionate, adipate, benzoate and the like where (a) is equal to the valence of X and (b) is from 1 to the valence of X.
- said fatty acid is a linear or branched chain aliphatic saturated or unsaturated fatty acid having from about 12 to about 22 carbon atoms based on coconut oil, vegetable oils, seed oils animal fats and fish oils;
- tertiary amines that can be employed in this regard include dimethylamino propyl amine, amino ethylanolamine, distearly methyl amine, dihydrogenated tallow methyl amine, ditallow methyl amine, dimethyl hydrogenated tallow amine, dimethyl coco amine, distearyl ethoxyethyl amine, stearyl bis-hydroxyethyl amine, stearyl bis (polyethoxy ethanol) amine, bis (tallowamidoethyl) 2-hydroxyethyl amine, bis (tallowamidoethyl) 2-hydroxylpropyl amine, 1-hydrogenated tallow amido ethyl -2-hydrogenated tallow imidazoline 1-ethylene bis (2tallow, 1-methyl, imidazolinium) dimethyl amino propyl tallow amidoamine and hydrogenated tallow hydroxyethyl imidazoline
- R 9 , R 10 , R 11 and R 12 are subsequently defined.
- Imidazoline compounds that may be used are also described in Demangeon (supra), whereas the quarternizing agents include;
- the quaternary ammonium compound thus obtained has the formula:
- R, R 1 , R 2 , R 3 , R 4 , R 5 , R 6 and R 7 have been defined above;
- a ⁇ is an anion based on R 7 (a ⁇ b) X or equivalent anions known in the quaternary ammonium compound art;
- R 9 is about C8 to C30, preferably about C12 to about C18 alkyl or akenyls alkenyl
- R 10 and R 11 are independently hydrogen or C1 to about C4 alkyl
- R 12 is C1 to about C4 alkyl
- m is about 2 to about 3
- a ⁇ is preferably an anion such as chloride, bromide, sulfate, methosulfate, nitrite, phosphate and carbosylate (i.e., acetate, adipate, propionate, benzoate)
- the tertiary amine salt has the formula:
- R 8 is a linear or a branched chain aliphatic saturated or unsaturated hydrocarbon group having from about 11 to about 21 carbon atoms.
- lower alkoxy, lower alkylene and lower alkyl are intended to include compounds having up to about 3 or about 4 carbon atoms including the various isomeric configurations thereof e.g. t-butyl, i-butyl, i-propyl and the like and the various mixtures thereof whether such mixtures of such groups contain components having one, or two, or three or four carbon atoms or more and also where such groups individually or in combination are in any of their isomeric forms.
- the tertiary amine, quaternizing agent and fatty acid are reacted with one another each in an amount so that the mixture obtained contains from about 10 weight percent to about 80 weight percent and especially from about 35 weight percent to about 55 weight percent of said quaternary ammonium compound, about 15 weight percent to about 70 weight percent and especially from about 10 weight percent to about 30 weight percent of said salt, about 1 weight percent to about 70 weight percent and especially from about 5 weight percent to about 25 weight percent of said ester and from about 5 weight percent to about 70 weight percent and especially from about 15 weight percent to about 35 weight percent of said fatty acid wherein the ratio of said quaternary ammonium compound to said salt is from about 2:1 to about 1:2.
- the method of the invention is preferably practiced so that the quaternary ammonium compound that is obtained has the structural formula (I) wherein at least one of R, R 1 and R 2 is a branched chain or linear aliphatic saturated or unsaturated hydrocarbon group having from about 12 to about 22 carbon atoms, preferably saturated, and especially those based on hard tallow acids (i.e. hydrogenated tallow fatty acids) and the balance, if any of the aforesaid R, R 1 and R 2 groups is a lower alkyl group and R 7 is a lower alkyl group.
- X is a sulfate group.
- the invention also relates to a mixture of the various quaternary ammonium compounds as described above in combination with the various fatty acid esters, fatty acids, and tertiary amine salts also as described previously and in the amounts and ratios as described previously.
- the invention also relates to a fabric softening article of manufacture comprising a fabric softening amount of any of the mixtures as described herein operatively associated with a substrate that will release such mixture to a fabric under fabric softening conditions encountered in a fabric or clothes dryer and includes the use of any of the aforesaid mixtures in a fabric softening relationship with a nonwoven or woven fiber or a polymeric open-celled or substantially open-celled foam substrate, such combination being prepared in a manner well known in the art.
- the mixture is employed in an amount from about 0.1 to about 10 gms and especially 1 to about 39 grms per 9 in. by 11 in. sheet.
- the various polymeric foams that are employed in this respect comprise polyurethane foams as well as any of the art known equivalent foams.
- the invention is directed to a fabric cleaning composition
- a detergent in combination with a fabric softening amount of any of the mixtures described herein.
- These detergents can be any of the art known anionic, cationic, nonionic or amphoteric synthetic detergents or wetting agents that are well known in the art or a soap i.e. the reaction product of a fatty acid with a alkaline hydroxide that is water soluble e.g. fatty acid reaction products of sodium, potassium or ammonium hydroxides or amines or the art known equivalents thereof.
- alkyl alcohol ethoxylates as well as those noted in the prior art cited.herein.
- the mixture of the invention is incorporated into the detergents (whether solid or liquid) by blending in a manner well known in the art.
- the amount of the mixture employed is any where from about 1 to about 50 and especially from about 2 to about 30 wt. % based on the quaternary ammonium compound and the active components of the detergent i.e. the component of the detergent that has both organophilic and hydrophilic groups.
- the amine was charged to a clean, dry reactor which was heated to 140° F. A slight nitrogen purge was employed over the amine that was charged to prevent it from coming into contact with any air that might enter into the reactor during the reaction.
- the stearic acid was then charged, mixed and heated to 140° F. after which the dimethyl sulfate was charged in increments sufficient to maintain the temperature of the reaction mixture at 140-170° F.
- the reaction is exothermic and the end point of the reaction is indicated to some degree when an exotherm is no longer obtained.
- the resultant mixture was allowed to cool.
- the foregoing method produced a reaction mixture which was analyzed by NMR analysis showing that the mixture obtained had the following components:
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Emergency Medicine (AREA)
- Dermatology (AREA)
- Detergent Compositions (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Abstract
Description
Components | M.W. | Moles | % by Wt. | ||
Dihydrogenated Tallow- | 523 | 1.00 | 56.63 | ||
Methyl-Amine | |||||
Stearic Acid | 30.00 | ||||
Dimethyl Sulfate | 126 | 0.98 | 13.37 | ||
% | ||
Quaternary Ammonium compound | 46 | ||
Fatty Acid | 22 | ||
Tertiary Amine and Amine Salt | 19 | ||
Methyl Ester | 13 | ||
Claims (17)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US09/330,621 USRE37555E1 (en) | 1990-01-31 | 1999-06-11 | Process and composition for multicomponent one hundred percent solid fabric softeners |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US47273890A | 1990-01-31 | 1990-01-31 | |
US07/793,216 US5221794A (en) | 1990-01-31 | 1991-11-07 | Process and composition for multicomponent one hundred percent solid fabric softeners |
US09/330,621 USRE37555E1 (en) | 1990-01-31 | 1999-06-11 | Process and composition for multicomponent one hundred percent solid fabric softeners |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US07/793,216 Reissue US5221794A (en) | 1990-01-31 | 1991-11-07 | Process and composition for multicomponent one hundred percent solid fabric softeners |
Publications (1)
Publication Number | Publication Date |
---|---|
USRE37555E1 true USRE37555E1 (en) | 2002-02-19 |
Family
ID=27043895
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US07/793,216 Ceased US5221794A (en) | 1990-01-31 | 1991-11-07 | Process and composition for multicomponent one hundred percent solid fabric softeners |
US09/330,621 Expired - Lifetime USRE37555E1 (en) | 1990-01-31 | 1999-06-11 | Process and composition for multicomponent one hundred percent solid fabric softeners |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US07/793,216 Ceased US5221794A (en) | 1990-01-31 | 1991-11-07 | Process and composition for multicomponent one hundred percent solid fabric softeners |
Country Status (1)
Country | Link |
---|---|
US (2) | US5221794A (en) |
Families Citing this family (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5298656A (en) * | 1991-03-25 | 1994-03-29 | Lenick Jr Anthony J O | Ester quaternary compounds |
GB9209170D0 (en) * | 1992-04-28 | 1992-06-10 | Unilever Plc | Rinse conditioner |
US5503756A (en) * | 1994-09-20 | 1996-04-02 | The Procter & Gamble Company | Dryer-activated fabric conditioning compositions containing unsaturated fatty acid |
NZ286025A (en) * | 1995-03-01 | 1997-04-24 | Colgate Palmolive Co | Laundry detergent concentrates; contains nonionic surfactant and water insoluble oil with a hydrophilic polar group, converts to liquid crystal phase dispersion on dilution |
US6287547B1 (en) * | 1999-10-12 | 2001-09-11 | Sanyo Chemical Industries, Ltd. | Hair treatment composition |
US20060234899A1 (en) * | 2003-03-05 | 2006-10-19 | H.H. Brown Shoe Technologies Inc. D/B/A Dicon Technologies | Hydrophilic polyurethane foam articles comprising an antimicrobial compound |
MX2009012912A (en) | 2007-06-15 | 2010-01-14 | Ecolab Inc | Liquid fabric conditioner composition and method of use. |
US8232239B2 (en) * | 2010-03-09 | 2012-07-31 | Ecolab Usa Inc. | Liquid concentrated fabric softener composition |
US8673838B2 (en) | 2011-06-22 | 2014-03-18 | Ecolab Usa Inc. | Solid concentrated fabric softener composition |
US9725679B2 (en) | 2014-11-21 | 2017-08-08 | Ecolab Usa Inc. | Compositions to boost fabric softener performance |
US9506015B2 (en) | 2014-11-21 | 2016-11-29 | Ecolab Usa Inc. | Compositions to boost fabric softener performance |
US9688945B2 (en) | 2014-11-21 | 2017-06-27 | Ecolab Usa Inc. | Compositions to boost fabric softener performance |
Citations (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2474202A (en) | 1946-01-10 | 1949-06-21 | Montclair Res Corp | Quaternary ammonium compounds and the process of making same |
US2583772A (en) | 1949-02-12 | 1952-01-29 | Dearborn Chemicals Co | Acid and quaternary salts of polyamides |
US3686025A (en) | 1968-12-30 | 1972-08-22 | Procter & Gamble | Textile softening agents impregnated into absorbent materials |
US3936537A (en) | 1974-11-01 | 1976-02-03 | The Procter & Gamble Company | Detergent-compatible fabric softening and antistatic compositions |
US4022938A (en) | 1974-04-16 | 1977-05-10 | The Procter & Gamble Company | Fabric treatment compositions |
US4237064A (en) | 1978-09-08 | 1980-12-02 | Akzona Incorporated | Process for preparing quaternary ammonium compositions |
US4238373A (en) | 1978-03-06 | 1980-12-09 | The Procter & Gamble Company | Process for making detergent compositions containing nitrogenous cationic surfactants |
EP0048163A2 (en) | 1980-09-17 | 1982-03-24 | Beecham Inc. | Fabric conditioning articles and methods of use |
US4832856A (en) | 1987-03-13 | 1989-05-23 | Henkel Kommanditgesellschaft Auf Aktien | Aqueous fabric softener for the treatment of fabrics: containing alkylamine, hydroxyalkylamine or quaternary ammonium derivative and a carboxylic acid |
US4844824A (en) | 1988-02-08 | 1989-07-04 | The Procter & Gamble Company | Stable heavy duty liquid detergent compositions which contain a softener and antistatic agent |
US4851141A (en) | 1984-12-12 | 1989-07-25 | Colgate-Palmolive Company | Concentrated stable nonaqueous fabric softener composition |
US4857213A (en) | 1988-02-08 | 1989-08-15 | The Procter & Gamble Company | Liquid detergent containing conditioning agent and high levels of alkyl sulfate/alkyl ethoxylated sulfate |
US4859456A (en) | 1985-12-23 | 1989-08-22 | Colgate-Palmolive Company | Hair rinse conditioners with superior dry hair feel and high hair luster |
EP0345495A2 (en) | 1988-05-27 | 1989-12-13 | Henkel Kommanditgesellschaft auf Aktien | Fabric softener |
EP0345475A1 (en) | 1988-05-13 | 1989-12-13 | Hoechst Aktiengesellschaft | Process for the production of quaternary ammonium salts of long-chain aliphatic carboxylic acids |
-
1991
- 1991-11-07 US US07/793,216 patent/US5221794A/en not_active Ceased
-
1999
- 1999-06-11 US US09/330,621 patent/USRE37555E1/en not_active Expired - Lifetime
Patent Citations (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2474202A (en) | 1946-01-10 | 1949-06-21 | Montclair Res Corp | Quaternary ammonium compounds and the process of making same |
US2583772A (en) | 1949-02-12 | 1952-01-29 | Dearborn Chemicals Co | Acid and quaternary salts of polyamides |
US3686025A (en) | 1968-12-30 | 1972-08-22 | Procter & Gamble | Textile softening agents impregnated into absorbent materials |
US4022938A (en) | 1974-04-16 | 1977-05-10 | The Procter & Gamble Company | Fabric treatment compositions |
US3936537A (en) | 1974-11-01 | 1976-02-03 | The Procter & Gamble Company | Detergent-compatible fabric softening and antistatic compositions |
US4238373A (en) | 1978-03-06 | 1980-12-09 | The Procter & Gamble Company | Process for making detergent compositions containing nitrogenous cationic surfactants |
US4237064B1 (en) | 1978-09-08 | 1986-02-11 | ||
US4237064A (en) | 1978-09-08 | 1980-12-02 | Akzona Incorporated | Process for preparing quaternary ammonium compositions |
EP0048163A2 (en) | 1980-09-17 | 1982-03-24 | Beecham Inc. | Fabric conditioning articles and methods of use |
US4851141A (en) | 1984-12-12 | 1989-07-25 | Colgate-Palmolive Company | Concentrated stable nonaqueous fabric softener composition |
US4859456A (en) | 1985-12-23 | 1989-08-22 | Colgate-Palmolive Company | Hair rinse conditioners with superior dry hair feel and high hair luster |
US4832856A (en) | 1987-03-13 | 1989-05-23 | Henkel Kommanditgesellschaft Auf Aktien | Aqueous fabric softener for the treatment of fabrics: containing alkylamine, hydroxyalkylamine or quaternary ammonium derivative and a carboxylic acid |
US4844824A (en) | 1988-02-08 | 1989-07-04 | The Procter & Gamble Company | Stable heavy duty liquid detergent compositions which contain a softener and antistatic agent |
US4857213A (en) | 1988-02-08 | 1989-08-15 | The Procter & Gamble Company | Liquid detergent containing conditioning agent and high levels of alkyl sulfate/alkyl ethoxylated sulfate |
EP0345475A1 (en) | 1988-05-13 | 1989-12-13 | Hoechst Aktiengesellschaft | Process for the production of quaternary ammonium salts of long-chain aliphatic carboxylic acids |
EP0345495A2 (en) | 1988-05-27 | 1989-12-13 | Henkel Kommanditgesellschaft auf Aktien | Fabric softener |
Also Published As
Publication number | Publication date |
---|---|
US5221794A (en) | 1993-06-22 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US5284650A (en) | Process for making high solids fabric softeners using low amounts of solvents and eliminating side reactions | |
US3775316A (en) | Softening finishes for washed laundry | |
EP0293955B1 (en) | Quaternary isopropyl ester ammonium compounds as fiber and fabric treatment compositions | |
USRE37555E1 (en) | Process and composition for multicomponent one hundred percent solid fabric softeners | |
EP0729344B1 (en) | Active substance delivery system | |
US4327133A (en) | Additives for clothes dryers | |
US4851138A (en) | Fabric softening composition and detergent-composition comprising the same | |
US4012326A (en) | Additives for clothes dryers | |
KR950003851B1 (en) | Mono-ester as fiber and fabric treatment composition | |
US4965100A (en) | Conditioning of fabrics | |
US4421792A (en) | Additives for clothes dryers | |
JPH0236712B2 (en) | ||
JPH0765267B2 (en) | Softening agent | |
EP0445525B1 (en) | Process for making high solids fabric softeners using low amounts of solvents and eliminating side reactions | |
JP2001512538A (en) | Softening active substance for woven fabric and softening composition for woven fabric containing the same | |
WO1990011838A1 (en) | Stearate-based dryer-added fabric softener sheet | |
EP0440229B1 (en) | Process and composition for multicomponent 100% solid fabric softeners | |
US5811385A (en) | High-concentration aqueous ester quat solutions | |
EP0643038A2 (en) | Novel polyfunctional cationic surface active agents, compositions comprised thereof, process for the preparation thereof and uses | |
US4623471A (en) | Aqueous textile washing compositions | |
JPH027994B2 (en) | ||
GB2260997A (en) | Fabric softener | |
JP2992419B2 (en) | Soft finish | |
AU2006263415B2 (en) | Oligomeric amidoamines or amidoquats for fabric or hair treatment compositions | |
JP3021749B2 (en) | Liquid soft finish |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
AS | Assignment |
Owner name: WITCO CORPORATION, CONNECTICUT Free format text: MERGER;ASSIGNOR:SHEREX CHEMICAL COMPANY, INC.;REEL/FRAME:010032/0497 Effective date: 19970422 |
|
AS | Assignment |
Owner name: GOLDSCHMIDT CHEMICAL CORPORATION, VIRGINIA Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:GOLDSCHMIDT SKW OLEOCHEMICALS LLC;REEL/FRAME:011306/0636 Effective date: 19991231 Owner name: GODSCHMIDT SKW OLEOCHEMICALS LLC, VIRGINIA Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:WITCO CORPORATION;REEL/FRAME:011314/0722 Effective date: 19990830 |
|
REFU | Refund |
Free format text: REFUND - PAYMENT OF MAINTENANCE FEE, 12TH YEAR, LARGE ENTITY (ORIGINAL EVENT CODE: R1553); ENTITY STATUS OF PATENT OWNER: LARGE ENTITY |
|
FPAY | Fee payment |
Year of fee payment: 12 |
|
AS | Assignment |
Owner name: EVONIK GOLDSCHMIDT CORP.,VIRGINIA Free format text: CHANGE OF NAME;ASSIGNOR:GOLDSCHMIDT CHEMICAL CORP.;REEL/FRAME:023973/0615 Effective date: 20071108 |