GB1049100A - Plasticized acrylic ester resins - Google Patents
Plasticized acrylic ester resinsInfo
- Publication number
- GB1049100A GB1049100A GB3275563A GB3275563A GB1049100A GB 1049100 A GB1049100 A GB 1049100A GB 3275563 A GB3275563 A GB 3275563A GB 3275563 A GB3275563 A GB 3275563A GB 1049100 A GB1049100 A GB 1049100A
- Authority
- GB
- United Kingdom
- Prior art keywords
- esters
- acid
- acrylic
- plasticized
- ester
- 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
Links
- 229920005989 resin Polymers 0.000 title abstract 16
- 239000011347 resin Substances 0.000 title abstract 16
- -1 acrylic ester Chemical class 0.000 title abstract 11
- 150000002148 esters Chemical class 0.000 abstract 14
- 235000014113 dietary fatty acids Nutrition 0.000 abstract 13
- 239000000194 fatty acid Substances 0.000 abstract 13
- 229930195729 fatty acid Natural products 0.000 abstract 13
- 150000004665 fatty acids Chemical class 0.000 abstract 12
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 abstract 8
- 239000006185 dispersion Substances 0.000 abstract 7
- 239000004593 Epoxy Substances 0.000 abstract 6
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 abstract 6
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 abstract 6
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 abstract 6
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 abstract 6
- 238000010438 heat treatment Methods 0.000 abstract 6
- 239000000944 linseed oil Substances 0.000 abstract 6
- 235000021388 linseed oil Nutrition 0.000 abstract 6
- 239000003784 tall oil Substances 0.000 abstract 6
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 abstract 5
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 abstract 5
- 239000004014 plasticizer Substances 0.000 abstract 5
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 abstract 4
- 229920003180 amino resin Polymers 0.000 abstract 4
- 125000004432 carbon atom Chemical group C* 0.000 abstract 4
- 239000003549 soybean oil Substances 0.000 abstract 4
- 235000012424 soybean oil Nutrition 0.000 abstract 4
- 239000008096 xylene Substances 0.000 abstract 4
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 abstract 3
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 abstract 3
- 229910000906 Bronze Inorganic materials 0.000 abstract 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 3
- 239000004606 Fillers/Extenders Substances 0.000 abstract 3
- 239000005909 Kieselgur Substances 0.000 abstract 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 abstract 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract 3
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 abstract 3
- 239000002253 acid Substances 0.000 abstract 3
- 125000002015 acyclic group Chemical group 0.000 abstract 3
- 150000001299 aldehydes Chemical class 0.000 abstract 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 abstract 3
- 150000001408 amides Chemical group 0.000 abstract 3
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 abstract 3
- 239000010974 bronze Substances 0.000 abstract 3
- 239000006229 carbon black Substances 0.000 abstract 3
- 125000001309 chloro group Chemical group Cl* 0.000 abstract 3
- 125000004965 chloroalkyl group Chemical group 0.000 abstract 3
- ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical class [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 abstract 3
- 238000000576 coating method Methods 0.000 abstract 3
- KUNSUQLRTQLHQQ-UHFFFAOYSA-N copper tin Chemical compound [Cu].[Sn] KUNSUQLRTQLHQQ-UHFFFAOYSA-N 0.000 abstract 3
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 3
- 238000004821 distillation Methods 0.000 abstract 3
- 239000003995 emulsifying agent Substances 0.000 abstract 3
- 125000001033 ether group Chemical group 0.000 abstract 3
- 239000000945 filler Substances 0.000 abstract 3
- 235000021384 green leafy vegetables Nutrition 0.000 abstract 3
- 150000004679 hydroxides Chemical class 0.000 abstract 3
- 229910052742 iron Inorganic materials 0.000 abstract 3
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 abstract 3
- 229910044991 metal oxide Inorganic materials 0.000 abstract 3
- 150000004706 metal oxides Chemical class 0.000 abstract 3
- 239000000203 mixture Substances 0.000 abstract 3
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 abstract 3
- 239000000049 pigment Substances 0.000 abstract 3
- 229920000642 polymer Polymers 0.000 abstract 3
- 239000000843 powder Substances 0.000 abstract 3
- 235000005713 safflower oil Nutrition 0.000 abstract 3
- 239000003813 safflower oil Substances 0.000 abstract 3
- 150000004760 silicates Chemical class 0.000 abstract 3
- 238000005507 spraying Methods 0.000 abstract 3
- 150000003467 sulfuric acid derivatives Chemical class 0.000 abstract 3
- 239000000454 talc Substances 0.000 abstract 3
- 229910052623 talc Inorganic materials 0.000 abstract 3
- 150000003568 thioethers Chemical class 0.000 abstract 3
- 239000004408 titanium dioxide Substances 0.000 abstract 3
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 abstract 2
- NXQMCAOPTPLPRL-UHFFFAOYSA-N 2-(2-benzoyloxyethoxy)ethyl benzoate Chemical compound C=1C=CC=CC=1C(=O)OCCOCCOC(=O)C1=CC=CC=C1 NXQMCAOPTPLPRL-UHFFFAOYSA-N 0.000 abstract 2
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 abstract 2
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 abstract 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 abstract 2
- 229920000742 Cotton Polymers 0.000 abstract 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 abstract 2
- 239000005642 Oleic acid Substances 0.000 abstract 2
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 abstract 2
- KFSLWBXXFJQRDL-UHFFFAOYSA-N Peracetic acid Chemical compound CC(=O)OO KFSLWBXXFJQRDL-UHFFFAOYSA-N 0.000 abstract 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 abstract 2
- 229920000297 Rayon Polymers 0.000 abstract 2
- 235000019485 Safflower oil Nutrition 0.000 abstract 2
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 abstract 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 abstract 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 abstract 2
- 150000007513 acids Chemical class 0.000 abstract 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 125000003368 amide group Chemical group 0.000 abstract 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 abstract 2
- 239000011248 coating agent Substances 0.000 abstract 2
- 239000008199 coating composition Substances 0.000 abstract 2
- 239000007859 condensation product Substances 0.000 abstract 2
- 229920001577 copolymer Polymers 0.000 abstract 2
- 239000004744 fabric Substances 0.000 abstract 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 2
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 abstract 2
- 229910052751 metal Inorganic materials 0.000 abstract 2
- 239000002184 metal Substances 0.000 abstract 2
- 125000005395 methacrylic acid group Chemical class 0.000 abstract 2
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 abstract 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 abstract 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 2
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 abstract 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 abstract 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 2
- ZQHJVIHCDHJVII-OWOJBTEDSA-N (e)-2-chlorobut-2-enedioic acid Chemical compound OC(=O)\C=C(\Cl)C(O)=O ZQHJVIHCDHJVII-OWOJBTEDSA-N 0.000 abstract 1
- PACBIGNRUWABMA-UHFFFAOYSA-N 2-(2,3-dihydro-1,3-benzothiazol-2-yl)-6-dodecyl-4-methylphenol Chemical compound CCCCCCCCCCCCC1=CC(C)=CC(C2SC3=CC=CC=C3N2)=C1O PACBIGNRUWABMA-UHFFFAOYSA-N 0.000 abstract 1
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 abstract 1
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 abstract 1
- FTABYKMUGGJOES-UHFFFAOYSA-N 2-[6-(2-carboxybenzoyl)oxyhexoxycarbonyl]benzoic acid Chemical compound OC(=O)C1=CC=CC=C1C(=O)OCCCCCCOC(=O)C1=CC=CC=C1C(O)=O FTABYKMUGGJOES-UHFFFAOYSA-N 0.000 abstract 1
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 abstract 1
- 239000004808 2-ethylhexylester Substances 0.000 abstract 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 abstract 1
- KGIGUEBEKRSTEW-UHFFFAOYSA-N 2-vinylpyridine Chemical group C=CC1=CC=CC=N1 KGIGUEBEKRSTEW-UHFFFAOYSA-N 0.000 abstract 1
- QZCLKYGREBVARF-UHFFFAOYSA-N Acetyl tributyl citrate Chemical compound CCCCOC(=O)CC(C(=O)OCCCC)(OC(C)=O)CC(=O)OCCCC QZCLKYGREBVARF-UHFFFAOYSA-N 0.000 abstract 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical group C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 abstract 1
- 239000005711 Benzoic acid Substances 0.000 abstract 1
- GOJCZVPJCKEBQV-UHFFFAOYSA-N Butyl phthalyl butylglycolate Chemical compound CCCCOC(=O)COC(=O)C1=CC=CC=C1C(=O)OCCCC GOJCZVPJCKEBQV-UHFFFAOYSA-N 0.000 abstract 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 abstract 1
- 229920004934 Dacron® Polymers 0.000 abstract 1
- 229920000877 Melamine resin Polymers 0.000 abstract 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 abstract 1
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical group CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 abstract 1
- 239000004677 Nylon Substances 0.000 abstract 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 abstract 1
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 abstract 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 abstract 1
- 239000001089 [(2R)-oxolan-2-yl]methanol Substances 0.000 abstract 1
- 125000002877 alkyl aryl group Chemical group 0.000 abstract 1
- 125000004103 aminoalkyl group Chemical group 0.000 abstract 1
- 239000010775 animal oil Substances 0.000 abstract 1
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 235000010233 benzoic acid Nutrition 0.000 abstract 1
- 235000019445 benzyl alcohol Nutrition 0.000 abstract 1
- KCXMKQUNVWSEMD-UHFFFAOYSA-N benzyl chloride Chemical compound ClCC1=CC=CC=C1 KCXMKQUNVWSEMD-UHFFFAOYSA-N 0.000 abstract 1
- 229940073608 benzyl chloride Drugs 0.000 abstract 1
- 239000011230 binding agent Substances 0.000 abstract 1
- LBKFHGHXATXEBY-UHFFFAOYSA-N bis(1-methylcyclohexyl) benzene-1,2-dicarboxylate Chemical compound C=1C=CC=C(C(=O)OC2(C)CCCCC2)C=1C(=O)OC1(C)CCCCC1 LBKFHGHXATXEBY-UHFFFAOYSA-N 0.000 abstract 1
- OHJMTUPIZMNBFR-UHFFFAOYSA-N biuret Chemical compound NC(=O)NC(N)=O OHJMTUPIZMNBFR-UHFFFAOYSA-N 0.000 abstract 1
- 230000001680 brushing effect Effects 0.000 abstract 1
- 239000004202 carbamide Substances 0.000 abstract 1
- 239000000919 ceramic Substances 0.000 abstract 1
- 239000007795 chemical reaction product Substances 0.000 abstract 1
- HNEGQIOMVPPMNR-IHWYPQMZSA-N citraconic acid Chemical compound OC(=O)C(/C)=C\C(O)=O HNEGQIOMVPPMNR-IHWYPQMZSA-N 0.000 abstract 1
- 229940018557 citraconic acid Drugs 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 abstract 1
- QEFOHLDZJZYQEZ-UHFFFAOYSA-N dibutyl 2-(1,4-dibutoxy-1,4-dioxobutan-2-yl)sulfanylbutanedioate Chemical compound CCCCOC(=O)CC(C(=O)OCCCC)SC(C(=O)OCCCC)CC(=O)OCCCC QEFOHLDZJZYQEZ-UHFFFAOYSA-N 0.000 abstract 1
- 238000007598 dipping method Methods 0.000 abstract 1
- 238000001035 drying Methods 0.000 abstract 1
- 238000007590 electrostatic spraying Methods 0.000 abstract 1
- IGOFAIGWJGFDDZ-UHFFFAOYSA-N ethanesulfonamide;toluene Chemical compound CCS(N)(=O)=O.CC1=CC=CC=C1 IGOFAIGWJGFDDZ-UHFFFAOYSA-N 0.000 abstract 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
- XPNLOZNCOBKRNJ-UHFFFAOYSA-N ethyl prop-2-enoate;methyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C=C.COC(=O)C(C)=C XPNLOZNCOBKRNJ-UHFFFAOYSA-N 0.000 abstract 1
- 239000010685 fatty oil Substances 0.000 abstract 1
- 239000001530 fumaric acid Substances 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 150000002430 hydrocarbons Chemical group 0.000 abstract 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 abstract 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 abstract 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 abstract 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 abstract 1
- 150000004702 methyl esters Chemical class 0.000 abstract 1
- 210000000050 mohair Anatomy 0.000 abstract 1
- 150000002763 monocarboxylic acids Chemical class 0.000 abstract 1
- KKFHAJHLJHVUDM-UHFFFAOYSA-N n-vinylcarbazole Chemical compound C1=CC=C2N(C=C)C3=CC=CC=C3C2=C1 KKFHAJHLJHVUDM-UHFFFAOYSA-N 0.000 abstract 1
- 229920001778 nylon Polymers 0.000 abstract 1
- 235000021313 oleic acid Nutrition 0.000 abstract 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 abstract 1
- 150000003014 phosphoric acid esters Chemical class 0.000 abstract 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 abstract 1
- 229920002239 polyacrylonitrile Polymers 0.000 abstract 1
- 239000005020 polyethylene terephthalate Substances 0.000 abstract 1
- 229910000027 potassium carbonate Inorganic materials 0.000 abstract 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 abstract 1
- 239000002964 rayon Substances 0.000 abstract 1
- 239000011342 resin composition Substances 0.000 abstract 1
- 238000007761 roller coating Methods 0.000 abstract 1
- 150000003839 salts Chemical group 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- 239000000758 substrate Substances 0.000 abstract 1
- BSYVTEYKTMYBMK-UHFFFAOYSA-N tetrahydrofurfuryl alcohol Chemical compound OCC1CCCO1 BSYVTEYKTMYBMK-UHFFFAOYSA-N 0.000 abstract 1
- 239000004753 textile Substances 0.000 abstract 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 abstract 1
- 150000003918 triazines Chemical class 0.000 abstract 1
- 150000003672 ureas Chemical class 0.000 abstract 1
- 239000008158 vegetable oil Substances 0.000 abstract 1
- 235000013311 vegetables Nutrition 0.000 abstract 1
- 229920001567 vinyl ester resin Polymers 0.000 abstract 1
- 229920002554 vinyl polymer Polymers 0.000 abstract 1
- 150000008127 vinyl sulfides Chemical class 0.000 abstract 1
- 239000002023 wood Substances 0.000 abstract 1
- 210000002268 wool Anatomy 0.000 abstract 1
- 239000011787 zinc oxide Substances 0.000 abstract 1
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/263—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acids; Salts or esters thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D303/00—Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
- C07D303/02—Compounds containing oxirane rings
- C07D303/38—Compounds containing oxirane rings with hydrocarbon radicals, substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D303/40—Compounds containing oxirane rings with hydrocarbon radicals, substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals by ester radicals
- C07D303/42—Acyclic compounds having a chain of seven or more carbon atoms, e.g. epoxidised fats
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/04—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
- C07D307/10—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D307/12—Radicals substituted by oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/15—Heterocyclic compounds having oxygen in the ring
- C08K5/151—Heterocyclic compounds having oxygen in the ring having one oxygen atom in the ring
- C08K5/1515—Three-membered rings
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D133/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
- C09D133/04—Homopolymers or copolymers of esters
- C09D133/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
- C09D133/08—Homopolymers or copolymers of acrylic acid esters
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Health & Medical Sciences (AREA)
- Textile Engineering (AREA)
- Life Sciences & Earth Sciences (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Macromonomer-Based Addition Polymer (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US22008462A | 1962-08-28 | 1962-08-28 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1049100A true GB1049100A (en) | 1966-11-23 |
Family
ID=22821984
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB3275563A Expired GB1049100A (en) | 1962-08-28 | 1963-08-19 | Plasticized acrylic ester resins |
Country Status (4)
| Country | Link |
|---|---|
| BE (1) | BE636698A (enrdf_load_stackoverflow) |
| ES (1) | ES290609A1 (enrdf_load_stackoverflow) |
| GB (1) | GB1049100A (enrdf_load_stackoverflow) |
| NL (1) | NL296556A (enrdf_load_stackoverflow) |
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1991000895A1 (de) * | 1989-07-07 | 1991-01-24 | Basf Lacke + Farben Aktiengesellschaft | Verfahren zur herstellung einer mehrschichtigen lackierung und basislack zur herstellung der basisschicht einer mehrschichtigen lackierung |
| WO1998015685A1 (en) * | 1996-10-09 | 1998-04-16 | Hercules Incorporated | Ester lubricants as hydrophobic fiber finishes |
| WO1998028356A1 (de) * | 1996-12-24 | 1998-07-02 | Dlw Aktiengesellschaft | Polyreaktionsprodukte-enthaltendes material und verfahren zur herstellung |
| WO2000015708A1 (de) * | 1998-09-11 | 2000-03-23 | Ciba Specialty Chemicals Holding Inc. | Polymere zusammensetzung mit verbesserten glanzeigenschaften |
| WO2006014483A3 (en) * | 2004-07-08 | 2006-10-05 | Archer Daniels Midland Co | Epoxidized esters of vegetable oil fatty acids as reactive diluents |
| WO2011090812A2 (en) | 2010-01-22 | 2011-07-28 | Archer Daniels Midland Company | Processes for making high purity renewable source-based plasticizers and products made therefrom |
| EP3002301A1 (en) * | 2014-09-30 | 2016-04-06 | Rohm and Haas Company | Aqueous dispersion of composite particles |
| JP2016530384A (ja) * | 2013-09-06 | 2016-09-29 | スリーエム イノベイティブ プロパティズ カンパニー | 酸修飾したエポキシ化植物油及び（メタ）アクリルコポリマー硬化性組成物又は硬化した組成物 |
| CN113105806A (zh) * | 2021-04-08 | 2021-07-13 | 水利部交通运输部国家能源局南京水利科学研究院 | 一种用于海水淡化反应釜的镀膜材料制备和使用方法 |
-
0
- NL NL296556D patent/NL296556A/xx unknown
- BE BE636698D patent/BE636698A/xx unknown
-
1963
- 1963-08-06 ES ES290609A patent/ES290609A1/es not_active Expired
- 1963-08-19 GB GB3275563A patent/GB1049100A/en not_active Expired
Cited By (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1991000895A1 (de) * | 1989-07-07 | 1991-01-24 | Basf Lacke + Farben Aktiengesellschaft | Verfahren zur herstellung einer mehrschichtigen lackierung und basislack zur herstellung der basisschicht einer mehrschichtigen lackierung |
| WO1998015685A1 (en) * | 1996-10-09 | 1998-04-16 | Hercules Incorporated | Ester lubricants as hydrophobic fiber finishes |
| US5972497A (en) * | 1996-10-09 | 1999-10-26 | Fiberco, Inc. | Ester lubricants as hydrophobic fiber finishes |
| WO1998028356A1 (de) * | 1996-12-24 | 1998-07-02 | Dlw Aktiengesellschaft | Polyreaktionsprodukte-enthaltendes material und verfahren zur herstellung |
| US6150436A (en) * | 1996-12-24 | 2000-11-21 | Dlw Aktiengesellschaft | Material containing polyreactions products and method for the production thereof |
| WO2000015708A1 (de) * | 1998-09-11 | 2000-03-23 | Ciba Specialty Chemicals Holding Inc. | Polymere zusammensetzung mit verbesserten glanzeigenschaften |
| US6569926B1 (en) | 1998-09-11 | 2003-05-27 | Ciba Specialty Chemicals Corporation | Polymer compound with improved gloss properties |
| GB2431160A (en) * | 2004-07-08 | 2007-04-18 | Archer Daniels Midland Co | Epoxidized esters of vegetable oil fatty acids as reactive diluents |
| WO2006014483A3 (en) * | 2004-07-08 | 2006-10-05 | Archer Daniels Midland Co | Epoxidized esters of vegetable oil fatty acids as reactive diluents |
| WO2011090812A2 (en) | 2010-01-22 | 2011-07-28 | Archer Daniels Midland Company | Processes for making high purity renewable source-based plasticizers and products made therefrom |
| US20120277357A1 (en) * | 2010-01-22 | 2012-11-01 | Archer Daniels Midland Company | Processes for making high purity renewable source-based plasticizers and products made therefrom |
| WO2011090812A3 (en) * | 2010-01-22 | 2013-03-14 | Archer Daniels Midland Company | Processes for making high purity renewable source-based plasticizers and products made therefrom |
| US8703849B2 (en) * | 2010-01-22 | 2014-04-22 | Archer Daniels Midland Company | Processes for making high purity renewable source-based plasticizers and products made therefrom |
| JP2016530384A (ja) * | 2013-09-06 | 2016-09-29 | スリーエム イノベイティブ プロパティズ カンパニー | 酸修飾したエポキシ化植物油及び（メタ）アクリルコポリマー硬化性組成物又は硬化した組成物 |
| EP3002301A1 (en) * | 2014-09-30 | 2016-04-06 | Rohm and Haas Company | Aqueous dispersion of composite particles |
| US9587135B2 (en) | 2014-09-30 | 2017-03-07 | Dow Global Technologies Llc | Aqueous dispersion of composite particles |
| AU2015227422B2 (en) * | 2014-09-30 | 2019-08-01 | Dow Global Technologies Llc | Aqueous dispersion of composite particles |
| CN113105806A (zh) * | 2021-04-08 | 2021-07-13 | 水利部交通运输部国家能源局南京水利科学研究院 | 一种用于海水淡化反应釜的镀膜材料制备和使用方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| BE636698A (enrdf_load_stackoverflow) | |
| ES290609A1 (es) | 1963-12-16 |
| NL296556A (enrdf_load_stackoverflow) |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US4421889A (en) | Aqueous dispersion paints and process for making the same | |
| US3356627A (en) | Aqueous blends of two water-insoluble polymers, one of which has 1 to 15% of a monomer containing an alcoholic hydroxyl, amino, amido or ureido group | |
| US2915486A (en) | Polyester compositions, water-dispersible polyester-aminoplast condensation resins made therefrom, and methods for producing them | |
| GB1049100A (en) | Plasticized acrylic ester resins | |
| US3300429A (en) | Aqueous polymeric blends containing ureido monomer | |
| GB988473A (en) | Polymeric compositions | |
| US3969560A (en) | Copolymers of monounsaturated or diunsaturated polyesters with vinyl monomers | |
| US2886474A (en) | Compositions for binding pigments | |
| GB1104344A (en) | Unsaturated amides and polymers thereof | |
| GB766866A (en) | Improvements in or relating to synthetic resin dispersions and the preparation of impregnated sheet material therefrom | |
| GB1119667A (en) | Novel acrylic ester polymers | |
| US4069214A (en) | Novel curable composition | |
| US3386998A (en) | Nu-alkenoyloxy-2-morpholinones and their corresponding hydrolysis products | |
| US4128675A (en) | Process for treating textiles with reactive polymers | |
| GB962109A (en) | New copolymers and coating compositions thereof | |
| US3597268A (en) | Method of imparting soil resistance to synthetic textile materials and the resulting materials | |
| US3639539A (en) | Phosphorus-containing n n-dimethylolcarboxylic acid amides | |
| US4150945A (en) | Method of treating textiles with a curable composition of an acrylic copolymer | |
| DE2414428A1 (de) | Verfahren zum verkleben von fasern in vliesstoffen | |
| US2537667A (en) | Waterproofing of fibrous products | |
| JPS5859277A (ja) | 撥水撥油剤 | |
| US2282702A (en) | Dimethylene quaternary ammonium salts | |
| US3314927A (en) | Copolymers of alkylene polyaminesubstituted alkyl vinyl ethers and thioethers | |
| US3681108A (en) | Method of coating a fabric or textile with copolymers of monounsaturated or diunsaturated polyesters with vinyl monomers | |
| EP0329027A2 (en) | Epoxide crosslinkable latices |