JPH055880B2 - - Google Patents
Info
- Publication number
- JPH055880B2 JPH055880B2 JP58199875A JP19987583A JPH055880B2 JP H055880 B2 JPH055880 B2 JP H055880B2 JP 58199875 A JP58199875 A JP 58199875A JP 19987583 A JP19987583 A JP 19987583A JP H055880 B2 JPH055880 B2 JP H055880B2
- Authority
- JP
- Japan
- Prior art keywords
- moieties
- moiety
- aliphatic
- combinations
- group
- 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
- 239000010985 leather Substances 0.000 claims description 91
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 62
- 150000001875 compounds Chemical class 0.000 claims description 40
- 125000001931 aliphatic group Chemical group 0.000 claims description 38
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 34
- 125000006162 fluoroaliphatic group Chemical group 0.000 claims description 27
- 238000011282 treatment Methods 0.000 claims description 25
- 238000000034 method Methods 0.000 claims description 24
- 125000003118 aryl group Chemical group 0.000 claims description 20
- 150000003839 salts Chemical class 0.000 claims description 18
- 229910052783 alkali metal Inorganic materials 0.000 claims description 17
- 150000001340 alkali metals Chemical class 0.000 claims description 17
- 125000005842 heteroatom Chemical group 0.000 claims description 17
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 16
- 238000012545 processing Methods 0.000 claims description 16
- 239000006185 dispersion Substances 0.000 claims description 14
- 239000007787 solid Substances 0.000 claims description 5
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 claims description 4
- NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical compound FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 claims 1
- 239000000203 mixture Substances 0.000 description 29
- 239000003921 oil Substances 0.000 description 27
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 26
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 19
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 18
- 239000002253 acid Substances 0.000 description 15
- 239000003795 chemical substances by application Substances 0.000 description 15
- 238000006243 chemical reaction Methods 0.000 description 14
- 230000008569 process Effects 0.000 description 12
- 125000004432 carbon atom Chemical group C* 0.000 description 11
- 239000000243 solution Substances 0.000 description 10
- -1 perfluoroalkyl alkylene thiocarboxylic acids Chemical class 0.000 description 9
- 238000012360 testing method Methods 0.000 description 9
- 239000002585 base Substances 0.000 description 8
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 8
- 239000002243 precursor Substances 0.000 description 8
- 239000002904 solvent Substances 0.000 description 8
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 7
- 235000019441 ethanol Nutrition 0.000 description 7
- 230000003472 neutralizing effect Effects 0.000 description 7
- 150000007513 acids Chemical class 0.000 description 6
- 150000001735 carboxylic acids Chemical class 0.000 description 6
- 230000000149 penetrating effect Effects 0.000 description 6
- 239000007864 aqueous solution Substances 0.000 description 5
- 238000004043 dyeing Methods 0.000 description 5
- 239000000543 intermediate Substances 0.000 description 5
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 4
- 238000010521 absorption reaction Methods 0.000 description 4
- 235000019253 formic acid Nutrition 0.000 description 4
- 238000006386 neutralization reaction Methods 0.000 description 4
- 239000003960 organic solvent Substances 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- 239000000758 substrate Substances 0.000 description 4
- 210000002268 wool Anatomy 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 3
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 239000000908 ammonium hydroxide Substances 0.000 description 3
- 150000003863 ammonium salts Chemical class 0.000 description 3
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 3
- 239000003153 chemical reaction reagent Substances 0.000 description 3
- 150000001844 chromium Chemical class 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 239000000975 dye Substances 0.000 description 3
- 239000012948 isocyanate Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 230000035515 penetration Effects 0.000 description 3
- 238000003672 processing method Methods 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- 238000010992 reflux Methods 0.000 description 3
- 239000007921 spray Substances 0.000 description 3
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- DWHXNKJKNIHNOI-UHFFFAOYSA-N 10-azaniumylundecanoate Chemical compound CC(N)CCCCCCCCC(O)=O DWHXNKJKNIHNOI-UHFFFAOYSA-N 0.000 description 2
- KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical group NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 2
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- 239000000980 acid dye Substances 0.000 description 2
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- 150000001413 amino acids Chemical class 0.000 description 2
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 2
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 2
- 235000011130 ammonium sulphate Nutrition 0.000 description 2
- 239000012736 aqueous medium Substances 0.000 description 2
- 150000004657 carbamic acid derivatives Chemical class 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 125000005521 carbonamide group Chemical group 0.000 description 2
- 125000005708 carbonyloxy group Chemical group [*:2]OC([*:1])=O 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 125000005442 diisocyanate group Chemical group 0.000 description 2
- 238000010981 drying operation Methods 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 229910052731 fluorine Inorganic materials 0.000 description 2
- 239000011737 fluorine Substances 0.000 description 2
- 125000001153 fluoro group Chemical group F* 0.000 description 2
- 239000004811 fluoropolymer Substances 0.000 description 2
- 229920002313 fluoropolymer Polymers 0.000 description 2
- 230000002452 interceptive effect Effects 0.000 description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 230000002940 repellent Effects 0.000 description 2
- 239000005871 repellent Substances 0.000 description 2
- 230000000717 retained effect Effects 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000004753 textile Substances 0.000 description 2
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 2
- WWTBZEKOSBFBEM-SPWPXUSOSA-N (2s)-2-[[2-benzyl-3-[hydroxy-[(1r)-2-phenyl-1-(phenylmethoxycarbonylamino)ethyl]phosphoryl]propanoyl]amino]-3-(1h-indol-3-yl)propanoic acid Chemical compound N([C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)O)C(=O)C(CP(O)(=O)[C@H](CC=1C=CC=CC=1)NC(=O)OCC=1C=CC=CC=1)CC1=CC=CC=C1 WWTBZEKOSBFBEM-SPWPXUSOSA-N 0.000 description 1
- YBYBMKRSCHZIFU-UHFFFAOYSA-N 1,1,2,2,3,3,4,4,4-nonafluorobutyl prop-2-enoate Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(F)(F)OC(=O)C=C YBYBMKRSCHZIFU-UHFFFAOYSA-N 0.000 description 1
- KGRVJHAUYBGFFP-UHFFFAOYSA-N 2,2'-Methylenebis(4-methyl-6-tert-butylphenol) Chemical compound CC(C)(C)C1=CC(C)=CC(CC=2C(=C(C=C(C)C=2)C(C)(C)C)O)=C1O KGRVJHAUYBGFFP-UHFFFAOYSA-N 0.000 description 1
- PTBDIHRZYDMNKB-UHFFFAOYSA-N 2,2-Bis(hydroxymethyl)propionic acid Chemical compound OCC(C)(CO)C(O)=O PTBDIHRZYDMNKB-UHFFFAOYSA-N 0.000 description 1
- VXQBJTKSVGFQOL-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethyl acetate Chemical compound CCCCOCCOCCOC(C)=O VXQBJTKSVGFQOL-UHFFFAOYSA-N 0.000 description 1
- FALRKNHUBBKYCC-UHFFFAOYSA-N 2-(chloromethyl)pyridine-3-carbonitrile Chemical compound ClCC1=NC=CC=C1C#N FALRKNHUBBKYCC-UHFFFAOYSA-N 0.000 description 1
- ONIKNECPXCLUHT-UHFFFAOYSA-N 2-chlorobenzoyl chloride Chemical compound ClC(=O)C1=CC=CC=C1Cl ONIKNECPXCLUHT-UHFFFAOYSA-N 0.000 description 1
- GRJRKPMIRMSBNK-UHFFFAOYSA-N 3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctan-1-ol Chemical compound OCCC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F GRJRKPMIRMSBNK-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 102000008186 Collagen Human genes 0.000 description 1
- 108010035532 Collagen Proteins 0.000 description 1
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 239000004166 Lanolin Substances 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- CYTYCFOTNPOANT-UHFFFAOYSA-N Perchloroethylene Chemical group ClC(Cl)=C(Cl)Cl CYTYCFOTNPOANT-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 229920002732 Polyanhydride Polymers 0.000 description 1
- 229920002873 Polyethylenimine Polymers 0.000 description 1
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 1
- 239000004280 Sodium formate Substances 0.000 description 1
- 241001441726 Tetraodontiformes Species 0.000 description 1
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 1
- 244000130402 Waltheria indica Species 0.000 description 1
- 239000012445 acidic reagent Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 125000000477 aza group Chemical group 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 239000005388 borosilicate glass Substances 0.000 description 1
- 230000001680 brushing effect Effects 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 229920001436 collagen Polymers 0.000 description 1
- 229940126208 compound 22 Drugs 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 125000004956 cyclohexylene group Chemical group 0.000 description 1
- HHLUHHCJLNGYFC-UHFFFAOYSA-L dibutyltin(2+);dodecanoate;ethyl carbamate Chemical compound CCOC(N)=O.CCCC[Sn+2]CCCC.CCCCCCCCCCCC([O-])=O.CCCCCCCCCCCC([O-])=O HHLUHHCJLNGYFC-UHFFFAOYSA-L 0.000 description 1
- KORSJDCBLAPZEQ-UHFFFAOYSA-N dicyclohexylmethane-4,4'-diisocyanate Chemical compound C1CC(N=C=O)CCC1CC1CCC(N=C=O)CC1 KORSJDCBLAPZEQ-UHFFFAOYSA-N 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 230000008034 disappearance Effects 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000005485 electric heating Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 238000007730 finishing process Methods 0.000 description 1
- XUCNUKMRBVNAPB-UHFFFAOYSA-N fluoroethene Chemical group FC=C XUCNUKMRBVNAPB-UHFFFAOYSA-N 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- KKBDHDVJCJTZSH-UHFFFAOYSA-N furan-2,5-dione 3-methylideneoxolane-2,5-dione oxane-2,6-dione oxolane-2,5-dione Chemical class C1(C(=C)CC(=O)O1)=O.C1(CCCC(=O)O1)=O.C1(C=C/C(=O)O1)=O.C1(CCC(=O)O1)=O KKBDHDVJCJTZSH-UHFFFAOYSA-N 0.000 description 1
- 210000004209 hair Anatomy 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- 125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 125000001841 imino group Chemical group [H]N=* 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 238000002372 labelling Methods 0.000 description 1
- 229940039717 lanolin Drugs 0.000 description 1
- 235000019388 lanolin Nutrition 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- MKQLBNJQQZRQJU-UHFFFAOYSA-N morpholin-4-amine Chemical compound NN1CCOCC1 MKQLBNJQQZRQJU-UHFFFAOYSA-N 0.000 description 1
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 238000006053 organic reaction Methods 0.000 description 1
- 230000008520 organization Effects 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 239000005056 polyisocyanate Substances 0.000 description 1
- 229920001228 polyisocyanate Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000007790 scraping Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- HLBBKKJFGFRGMU-UHFFFAOYSA-M sodium formate Chemical compound [Na+].[O-]C=O HLBBKKJFGFRGMU-UHFFFAOYSA-M 0.000 description 1
- 235000019254 sodium formate Nutrition 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 229940014800 succinic anhydride Drugs 0.000 description 1
- QFARLUFBHFUZOK-UHFFFAOYSA-N sulfamoyl hydrogen sulfate Chemical compound NS(=O)(=O)OS(O)(=O)=O QFARLUFBHFUZOK-UHFFFAOYSA-N 0.000 description 1
- 229940124530 sulfonamide Drugs 0.000 description 1
- 150000003456 sulfonamides Chemical class 0.000 description 1
- 150000003457 sulfones Chemical class 0.000 description 1
- 229950011008 tetrachloroethylene Drugs 0.000 description 1
- 125000005628 tolylene group Chemical group 0.000 description 1
- UBOXGVDOUJQMTN-UHFFFAOYSA-N trichloroethylene Natural products ClCC(Cl)Cl UBOXGVDOUJQMTN-UHFFFAOYSA-N 0.000 description 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
- 150000003673 urethanes Chemical class 0.000 description 1
- 230000004584 weight gain Effects 0.000 description 1
- 235000019786 weight gain Nutrition 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C14—SKINS; HIDES; PELTS; LEATHER
- C14C—CHEMICAL TREATMENT OF HIDES, SKINS OR LEATHER, e.g. TANNING, IMPREGNATING, FINISHING; APPARATUS THEREFOR; COMPOSITIONS FOR TANNING
- C14C3/00—Tanning; Compositions for tanning
- C14C3/02—Chemical tanning
-
- C—CHEMISTRY; METALLURGY
- C14—SKINS; HIDES; PELTS; LEATHER
- C14C—CHEMICAL TREATMENT OF HIDES, SKINS OR LEATHER, e.g. TANNING, IMPREGNATING, FINISHING; APPARATUS THEREFOR; COMPOSITIONS FOR TANNING
- C14C9/00—Impregnating leather for preserving, waterproofing, making resistant to heat or similar purposes
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Treatment And Processing Of Natural Fur Or Leather (AREA)
- Materials Applied To Surfaces To Minimize Adherence Of Mist Or Water (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US06/436,267 US4525305A (en) | 1982-10-25 | 1982-10-25 | Leather with fluorochemical finish |
| US436267 | 1982-10-25 |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP4241255A Division JP2773012B2 (ja) | 1982-10-25 | 1992-08-18 | フルオロケミカル化合物 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS59104353A JPS59104353A (ja) | 1984-06-16 |
| JPH055880B2 true JPH055880B2 (d) | 1993-01-25 |
Family
ID=23731785
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP58199875A Granted JPS59104353A (ja) | 1982-10-25 | 1983-10-25 | フルオロケミカル加工なめし皮 |
| JP4241255A Expired - Lifetime JP2773012B2 (ja) | 1982-10-25 | 1992-08-18 | フルオロケミカル化合物 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP4241255A Expired - Lifetime JP2773012B2 (ja) | 1982-10-25 | 1992-08-18 | フルオロケミカル化合物 |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US4525305A (d) |
| EP (1) | EP0107948B1 (d) |
| JP (2) | JPS59104353A (d) |
| KR (1) | KR910001762B1 (d) |
| AR (1) | AR241699A1 (d) |
| AU (1) | AU565304B2 (d) |
| BR (1) | BR8305865A (d) |
| DE (1) | DE3370495D1 (d) |
| ES (1) | ES8602167A1 (d) |
| PT (1) | PT77553B (d) |
Families Citing this family (34)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4841090A (en) * | 1982-06-11 | 1989-06-20 | Minnesota Mining And Manufacturing Company | Treatment of fibrous substrates, such as carpet, with fluorochemical |
| DE3380930D1 (de) * | 1982-11-09 | 1990-01-11 | Minnesota Mining & Mfg | Substituierte guanidine die fluoraliphatische radikale enthalten und sie enthaltendes fibroeses material. |
| AU582346B2 (en) * | 1983-09-13 | 1989-03-23 | Minnesota Mining And Manufacturing Company | Fluorohydrocarbon sulfonamide compounds and use thereof in treatment of leather, textiles and cellusosic materials |
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| US4566981A (en) * | 1984-03-30 | 1986-01-28 | Minnesota Mining And Manufacturing Company | Fluorochemicals and fibrous substrates treated therewith: compositions of cationic and non-ionic fluorochemicals |
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| EP0235307A1 (en) * | 1986-01-03 | 1987-09-09 | Fa. YOSHINAGA PRINCE CO., LTD. | Method for waterproofing treatment of leather |
| DE3622284A1 (de) * | 1986-07-03 | 1988-01-07 | Hoechst Ag | Urethane aus aliphatischen fluoralkoholen, isocyanaten und aromatischen verbindungen, verfahren zu ihrer herstellung und ihre verwendung |
| DE3728162A1 (de) * | 1987-08-24 | 1989-03-09 | Hoechst Ag | Verfahren zur hydrophobierung und olephobierung von leder durch impraegnierung mit fluorchemikalien |
| DE3943127A1 (de) * | 1989-12-28 | 1991-07-04 | Hoechst Ag | Urethane als aliphatischen fluoralkoholen, isocyanaten und carbonsaeuren, verfahren zu ihrer herstellung und ihre verwendung |
| US5256318A (en) * | 1990-04-07 | 1993-10-26 | Daikin Industries Ltd. | Leather treatment and process for treating leather |
| US5188747A (en) * | 1990-09-04 | 1993-02-23 | Matsushita Electric Industrial Co., Ltd. | Fluorine-containing lubricant compounds |
| US5266724A (en) * | 1990-09-04 | 1993-11-30 | Matsushita Electric Industrial Co., Ltd. | Fluorine-containing compounds |
| US5120364A (en) * | 1990-10-10 | 1992-06-09 | Ciba-Geigy Corporation | Heteroatom containing perfluoroalkyl terminated neopentyl sulfates and salts thereof |
| JP3030863B2 (ja) * | 1990-12-25 | 2000-04-10 | ダイキン工業株式会社 | 皮革改質剤、皮革の改質方法および改質なめし皮革 |
| US6309752B1 (en) | 1991-04-02 | 2001-10-30 | 3M Innovative Properties Company | Substrate having high initial water repellency and a laundry durable water repellency |
| US5276175A (en) * | 1991-04-02 | 1994-01-04 | Minnesota Mining And Manufacturing Company | Isocyanate derivatives comprising flourochemical oligomers |
| DE4201800A1 (de) * | 1992-01-23 | 1993-07-29 | Wacker Chemie Gmbh | Beschichtung von substratoberflaechen |
| DE4244951C2 (de) * | 1992-12-01 | 1998-08-06 | Minnesota Mining & Mfg | Fasersubstrat mit Wasser-, Öl-, Schmutzabweisungsvermögen und Weichgriffigkeit |
| CA2141646C (en) * | 1994-02-04 | 2001-11-06 | Nobuyuki Kuwabara | Leather coloring process, leather coloring apparatus, and colored leather produced by such process |
| US5496642A (en) * | 1994-05-09 | 1996-03-05 | Olin Corporation | Low VOC, fluorocompound-containing one-component and two-component coating compositions for slippery coatings |
| US6294103B1 (en) | 1996-11-07 | 2001-09-25 | 3M Innovative Properties Company | Use of amphiphilic copolymers containing a fluorinated monomer to impart waterproofness to leather |
| EP0841405B1 (en) | 1996-11-07 | 1999-12-29 | Minnesota Mining And Manufacturing Company | Use of amphilic copolymers containing a fluorinated monomer to impart waterproofness to leather |
| US7049379B2 (en) * | 1999-05-11 | 2006-05-23 | 3M Innovative Properties Company | Alkylated fluorochemical oligomers and use thereof in the treatment of fibrous substrates |
| US6525127B1 (en) | 1999-05-11 | 2003-02-25 | 3M Innovative Properties Company | Alkylated fluorochemical oligomers and use thereof in the treatment of fibrous substrates |
| US6737489B2 (en) * | 2001-05-21 | 2004-05-18 | 3M Innovative Properties Company | Polymers containing perfluorovinyl ethers and applications for such polymers |
| US7045571B2 (en) * | 2001-05-21 | 2006-05-16 | 3M Innovative Properties Company | Emulsion polymerization of fluorinated monomers |
| JP2003096308A (ja) * | 2001-09-25 | 2003-04-03 | Asahi Glass Co Ltd | 撥水撥油性組成物およびその造形品 |
| USD526489S1 (en) * | 2003-04-17 | 2006-08-15 | Kaptain Kirk Kirkland | Surface pattern for leather goods |
| CA2574094A1 (en) * | 2004-08-03 | 2006-02-09 | Daikin Industries, Ltd. | Fluorine-containing urethanes |
| WO2009115539A1 (de) * | 2008-03-18 | 2009-09-24 | Basf Se | Metallcarbamate aus tolylendiaminen |
| WO2009115537A1 (de) * | 2008-03-18 | 2009-09-24 | Basf Se | Metallcarbamate aus diaminophenylmethan |
| CN108003061B (zh) * | 2016-10-27 | 2020-09-18 | 中国石油化工股份有限公司 | 一种具有增稠作用的化合物和润滑脂以及它们的制备方法 |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2934450A (en) * | 1955-12-29 | 1960-04-26 | Minnesota Mining & Mfg | Chromium complexes of fluorocarbon acids and articles coated therewith |
| DE1468295A1 (de) * | 1960-09-02 | 1969-05-29 | Minnesota Mining & Mfg | Perfluoralkylgruppen enthaltende Urethane und Verfahren zu deren Herstellung |
| US3238235A (en) * | 1963-04-29 | 1966-03-01 | Pennsalt Chemicals Corp | Fluorinated amido carboxylic acids and salts thereof |
| FR1396008A (fr) * | 1964-04-22 | 1965-04-16 | Pennsalt Chemicals Corp | Amides substitués d'acides carboxyliques halogénés à chaîne longue |
| US3382097A (en) * | 1964-07-30 | 1968-05-07 | Air Prod & Chem | Process of treating textiles and other materials with fluorinated organic amido acid compounds to impart repellency |
| US3471518A (en) * | 1967-07-10 | 1969-10-07 | Pennsalt Chemicals Corp | Fluoroalkyl dicarboxylic acids and derivatives |
| US3524760A (en) * | 1967-11-24 | 1970-08-18 | Du Pont | Process for imparting oil and water repellency to leathers |
| US3651105A (en) * | 1968-11-01 | 1972-03-21 | Allied Chem | Chromium complexes of fluoroisoalkoxyalkyl carboxylic acids |
| US3879440A (en) * | 1968-11-08 | 1975-04-22 | Allied Chem | Tertiary amine sulfamic acid salts of polyfluoroisoalkoxyalkyl carbamates |
| US3574518A (en) * | 1968-12-11 | 1971-04-13 | Minnesota Mining & Mfg | Collagen matrix waterproofing with chromium complexes containing radicals of long chain hydrocarbons and fluorinated hydrocarbons and product so produced |
| US3852313A (en) * | 1969-10-17 | 1974-12-03 | Allied Chem | Novel fluorocarbon acids |
| US4289892A (en) * | 1970-03-03 | 1981-09-15 | Minnesota Mining And Manufacturing Company | Fluorochemical foam stabilizer and foamed polyurethanes made therewith |
| US3907576A (en) * | 1972-02-22 | 1975-09-23 | Ciba Geigy Corp | Compositions containing werner complexes of chromium and fluorinated carboxylic acids |
| US4043923A (en) * | 1974-02-26 | 1977-08-23 | Minnesota Mining And Manufacturing Company | Textile treatment composition |
| US4035506A (en) * | 1974-07-26 | 1977-07-12 | Minnesota Mining And Manufacturing Company | Fluorocarbon dermal protective compositions |
| US4215205A (en) * | 1977-01-12 | 1980-07-29 | Minnesota Mining And Manufacturing Company | Fluoroaliphatic radical and carbodiimide containing compositions for fabric treatment |
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| FR2442861A1 (fr) * | 1978-11-14 | 1980-06-27 | Ugine Kuhlmann | Nouveaux produits fluores destines aux traitements oleofuges et hydrofuges de substrats divers et plus particulierement de substrats fibreux |
| US4340749A (en) * | 1979-12-21 | 1982-07-20 | Minnesota Mining And Manufacturing Company | Carpet treatment |
-
1982
- 1982-10-25 US US06/436,267 patent/US4525305A/en not_active Expired - Lifetime
-
1983
- 1983-10-13 AR AR83294534A patent/AR241699A1/es active
- 1983-10-17 DE DE8383306286T patent/DE3370495D1/de not_active Expired
- 1983-10-17 EP EP83306286A patent/EP0107948B1/en not_active Expired
- 1983-10-21 ES ES526635A patent/ES8602167A1/es not_active Expired
- 1983-10-24 AU AU20507/83A patent/AU565304B2/en not_active Ceased
- 1983-10-24 PT PT77553A patent/PT77553B/pt unknown
- 1983-10-24 BR BR8305865A patent/BR8305865A/pt not_active IP Right Cessation
- 1983-10-25 KR KR1019830005039A patent/KR910001762B1/ko not_active Expired
- 1983-10-25 JP JP58199875A patent/JPS59104353A/ja active Granted
-
1992
- 1992-08-18 JP JP4241255A patent/JP2773012B2/ja not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| DE3370495D1 (en) | 1987-04-30 |
| JPS59104353A (ja) | 1984-06-16 |
| PT77553A (en) | 1983-11-01 |
| KR910001762B1 (ko) | 1991-03-23 |
| ES526635A0 (es) | 1985-11-01 |
| EP0107948B1 (en) | 1987-03-25 |
| AU565304B2 (en) | 1987-09-10 |
| BR8305865A (pt) | 1984-05-29 |
| AU2050783A (en) | 1984-05-03 |
| AR241699A1 (es) | 1992-11-30 |
| PT77553B (en) | 1986-02-12 |
| JP2773012B2 (ja) | 1998-07-09 |
| EP0107948A1 (en) | 1984-05-09 |
| JPH06312971A (ja) | 1994-11-08 |
| KR840006503A (ko) | 1984-11-30 |
| ES8602167A1 (es) | 1985-11-01 |
| US4525305A (en) | 1985-06-25 |
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