CN103946317B - 氧化聚合型不饱和树脂用固化促进剂、印刷油墨及涂料 - Google Patents
氧化聚合型不饱和树脂用固化促进剂、印刷油墨及涂料 Download PDFInfo
- Publication number
- CN103946317B CN103946317B CN201280057560.XA CN201280057560A CN103946317B CN 103946317 B CN103946317 B CN 103946317B CN 201280057560 A CN201280057560 A CN 201280057560A CN 103946317 B CN103946317 B CN 103946317B
- Authority
- CN
- China
- Prior art keywords
- acid
- aliphatic acid
- resin
- oxidation polymerization
- curing accelerator
- 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.)
- Active
Links
- 229920005989 resin Polymers 0.000 title claims abstract description 73
- 239000011347 resin Substances 0.000 title claims abstract description 73
- 238000006116 polymerization reaction Methods 0.000 title claims abstract description 71
- 230000003647 oxidation Effects 0.000 title claims abstract description 66
- 238000007254 oxidation reaction Methods 0.000 title claims abstract description 66
- 238000000576 coating method Methods 0.000 title claims abstract description 42
- 239000011248 coating agent Substances 0.000 title claims abstract description 41
- 239000002253 acid Substances 0.000 claims abstract description 117
- 125000001931 aliphatic group Chemical group 0.000 claims abstract description 89
- -1 FFA bismuth salt Chemical class 0.000 claims abstract description 41
- 239000000203 mixture Substances 0.000 claims abstract description 33
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 21
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 21
- 150000002696 manganese Chemical class 0.000 claims abstract description 17
- 150000001414 amino alcohols Chemical class 0.000 claims abstract description 16
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 claims abstract description 15
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 14
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 10
- 159000000009 barium salts Chemical class 0.000 claims abstract description 9
- 125000001118 alkylidene group Chemical group 0.000 claims abstract description 7
- 125000004430 oxygen atom Chemical group O* 0.000 claims abstract description 5
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 34
- 239000000194 fatty acid Substances 0.000 claims description 34
- 229930195729 fatty acid Natural products 0.000 claims description 34
- FBUKVWPVBMHYJY-UHFFFAOYSA-N nonanoic acid Chemical compound CCCCCCCCC(O)=O FBUKVWPVBMHYJY-UHFFFAOYSA-N 0.000 claims description 16
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 15
- 229910052751 metal Inorganic materials 0.000 claims description 15
- 239000002184 metal Substances 0.000 claims description 15
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 claims description 11
- 235000019197 fats Nutrition 0.000 claims description 10
- YPIFGDQKSSMYHQ-UHFFFAOYSA-N 7,7-dimethyloctanoic acid Chemical compound CC(C)(C)CCCCCC(O)=O YPIFGDQKSSMYHQ-UHFFFAOYSA-N 0.000 claims description 9
- 244000068988 Glycine max Species 0.000 claims description 8
- 235000010469 Glycine max Nutrition 0.000 claims description 8
- RSWGJHLUYNHPMX-UHFFFAOYSA-N 1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylic acid Chemical compound C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 claims description 7
- 150000007513 acids Chemical group 0.000 claims description 7
- CUXYLFPMQMFGPL-UHFFFAOYSA-N (9Z,11E,13E)-9,11,13-Octadecatrienoic acid Natural products CCCCC=CC=CC=CCCCCCCCC(O)=O CUXYLFPMQMFGPL-UHFFFAOYSA-N 0.000 claims description 6
- OYHQOLUKZRVURQ-NTGFUMLPSA-N (9Z,12Z)-9,10,12,13-tetratritiooctadeca-9,12-dienoic acid Chemical compound C(CCCCCCC\C(=C(/C\C(=C(/CCCCC)\[3H])\[3H])\[3H])\[3H])(=O)O OYHQOLUKZRVURQ-NTGFUMLPSA-N 0.000 claims description 6
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 claims description 6
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 claims description 6
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 claims description 6
- 239000005642 Oleic acid Substances 0.000 claims description 6
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 claims description 6
- CUXYLFPMQMFGPL-SUTYWZMXSA-N all-trans-octadeca-9,11,13-trienoic acid Chemical compound CCCC\C=C\C=C\C=C\CCCCCCCC(O)=O CUXYLFPMQMFGPL-SUTYWZMXSA-N 0.000 claims description 6
- 150000001621 bismuth Chemical class 0.000 claims description 6
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 claims description 6
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 claims description 6
- 159000000008 strontium salts Chemical class 0.000 claims description 5
- 101150108864 Ffar1 gene Proteins 0.000 claims description 3
- 101100264077 Xenopus laevis wrn gene Proteins 0.000 claims description 3
- LYDPKGIUPHFQFP-UHFFFAOYSA-N 1-(4-aminobutylamino)ethanol Chemical compound CC(O)NCCCCN LYDPKGIUPHFQFP-UHFFFAOYSA-N 0.000 claims description 2
- YSAANLSYLSUVHB-UHFFFAOYSA-N 2-[2-(dimethylamino)ethoxy]ethanol Chemical compound CN(C)CCOCCO YSAANLSYLSUVHB-UHFFFAOYSA-N 0.000 claims description 2
- LSYBWANTZYUTGJ-UHFFFAOYSA-N 2-[2-(dimethylamino)ethyl-methylamino]ethanol Chemical compound CN(C)CCN(C)CCO LSYBWANTZYUTGJ-UHFFFAOYSA-N 0.000 claims description 2
- 239000003784 tall oil Substances 0.000 claims description 2
- 229910052788 barium Inorganic materials 0.000 claims 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 claims 1
- 229910017052 cobalt Inorganic materials 0.000 abstract description 22
- 239000010941 cobalt Substances 0.000 abstract description 22
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 abstract description 20
- 239000000344 soap Substances 0.000 abstract description 17
- 238000001035 drying Methods 0.000 description 22
- 229920000180 alkyd Polymers 0.000 description 20
- 239000002904 solvent Substances 0.000 description 16
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 15
- 150000004665 fatty acids Chemical class 0.000 description 14
- 239000003921 oil Substances 0.000 description 13
- 235000019198 oils Nutrition 0.000 description 13
- 150000005846 sugar alcohols Polymers 0.000 description 12
- 239000004593 Epoxy Substances 0.000 description 10
- UQDUPQYQJKYHQI-UHFFFAOYSA-N methyl laurate Chemical compound CCCCCCCCCCCC(=O)OC UQDUPQYQJKYHQI-UHFFFAOYSA-N 0.000 description 10
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 9
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- 229910052748 manganese Inorganic materials 0.000 description 9
- 239000002994 raw material Substances 0.000 description 9
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 8
- 150000002148 esters Chemical class 0.000 description 8
- 239000011572 manganese Substances 0.000 description 8
- 238000004519 manufacturing process Methods 0.000 description 8
- NUKZAGXMHTUAFE-UHFFFAOYSA-N methyl hexanoate Chemical compound CCCCCC(=O)OC NUKZAGXMHTUAFE-UHFFFAOYSA-N 0.000 description 8
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 7
- 230000002378 acidificating effect Effects 0.000 description 7
- 239000003822 epoxy resin Substances 0.000 description 7
- 229910052500 inorganic mineral Inorganic materials 0.000 description 7
- 239000011707 mineral Substances 0.000 description 7
- 229920000647 polyepoxide Polymers 0.000 description 7
- 235000015096 spirit Nutrition 0.000 description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 6
- 239000003085 diluting agent Substances 0.000 description 6
- YRHYCMZPEVDGFQ-UHFFFAOYSA-N methyl decanoate Chemical compound CCCCCCCCCC(=O)OC YRHYCMZPEVDGFQ-UHFFFAOYSA-N 0.000 description 6
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
- 239000000049 pigment Substances 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 6
- 206010007269 Carcinogenicity Diseases 0.000 description 5
- 229910052797 bismuth Inorganic materials 0.000 description 5
- 230000007670 carcinogenicity Effects 0.000 description 5
- 231100000260 carcinogenicity Toxicity 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 5
- 238000013329 compounding Methods 0.000 description 5
- 230000008602 contraction Effects 0.000 description 5
- 238000011156 evaluation Methods 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 239000001301 oxygen Substances 0.000 description 5
- 229910052760 oxygen Inorganic materials 0.000 description 5
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 4
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 4
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 4
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 4
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 4
- 150000001298 alcohols Chemical class 0.000 description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 4
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 description 4
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 4
- 230000032050 esterification Effects 0.000 description 4
- 238000005886 esterification reaction Methods 0.000 description 4
- 239000004519 grease Substances 0.000 description 4
- 229940043265 methyl isobutyl ketone Drugs 0.000 description 4
- 239000000178 monomer Substances 0.000 description 4
- 229920005749 polyurethane resin Polymers 0.000 description 4
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 4
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 3
- 229920002799 BoPET Polymers 0.000 description 3
- 239000004215 Carbon black (E152) Substances 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- 239000005041 Mylar™ Substances 0.000 description 3
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 3
- 239000004359 castor oil Substances 0.000 description 3
- 235000019438 castor oil Nutrition 0.000 description 3
- 238000004040 coloring Methods 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 235000011187 glycerol Nutrition 0.000 description 3
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 3
- 229940051250 hexylene glycol Drugs 0.000 description 3
- 235000003642 hunger Nutrition 0.000 description 3
- 229930195733 hydrocarbon Natural products 0.000 description 3
- 150000002430 hydrocarbons Chemical class 0.000 description 3
- 239000012948 isocyanate Substances 0.000 description 3
- 150000002576 ketones Chemical class 0.000 description 3
- 239000000944 linseed oil Substances 0.000 description 3
- 235000021388 linseed oil Nutrition 0.000 description 3
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 3
- 230000008929 regeneration Effects 0.000 description 3
- 238000011069 regeneration method Methods 0.000 description 3
- SBASXUCJHJRPEV-UHFFFAOYSA-N 2-(2-methoxyethoxy)ethanol Chemical compound COCCOCCO SBASXUCJHJRPEV-UHFFFAOYSA-N 0.000 description 2
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 2
- SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 description 2
- FJKROLUGYXJWQN-UHFFFAOYSA-N 4-hydroxybenzoic acid Chemical compound OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 2
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 244000020518 Carthamus tinctorius Species 0.000 description 2
- 235000003255 Carthamus tinctorius Nutrition 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- 235000019484 Rapeseed oil Nutrition 0.000 description 2
- 235000019485 Safflower oil Nutrition 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-N alpha-methacrylic acid Natural products CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 2
- 150000008064 anhydrides Chemical class 0.000 description 2
- 150000001622 bismuth compounds Chemical class 0.000 description 2
- 229940106691 bisphenol a Drugs 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 239000003240 coconut oil Substances 0.000 description 2
- 235000019864 coconut oil Nutrition 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 2
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 2
- 229940043237 diethanolamine Drugs 0.000 description 2
- 125000005442 diisocyanate group Chemical group 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- POLCUAVZOMRGSN-UHFFFAOYSA-N dipropyl ether Chemical compound CCCOCCC POLCUAVZOMRGSN-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 150000002118 epoxides Chemical class 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- RGXWDWUGBIJHDO-UHFFFAOYSA-N ethyl decanoate Chemical compound CCCCCCCCCC(=O)OCC RGXWDWUGBIJHDO-UHFFFAOYSA-N 0.000 description 2
- SHZIWNPUGXLXDT-UHFFFAOYSA-N ethyl hexanoate Chemical compound CCCCCC(=O)OCC SHZIWNPUGXLXDT-UHFFFAOYSA-N 0.000 description 2
- MMXKVMNBHPAILY-UHFFFAOYSA-N ethyl laurate Chemical compound CCCCCCCCCCCC(=O)OCC MMXKVMNBHPAILY-UHFFFAOYSA-N 0.000 description 2
- BYEVBITUADOIGY-UHFFFAOYSA-N ethyl nonanoate Chemical compound CCCCCCCCC(=O)OCC BYEVBITUADOIGY-UHFFFAOYSA-N 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 239000011630 iodine Substances 0.000 description 2
- 229910052740 iodine Inorganic materials 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- IJXHLVMUNBOGRR-UHFFFAOYSA-N methyl nonanoate Chemical compound CCCCCCCCC(=O)OC IJXHLVMUNBOGRR-UHFFFAOYSA-N 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 229920001707 polybutylene terephthalate Polymers 0.000 description 2
- 229920005644 polyethylene terephthalate glycol copolymer Polymers 0.000 description 2
- 239000005056 polyisocyanate Substances 0.000 description 2
- 229920001228 polyisocyanate Polymers 0.000 description 2
- 229920005862 polyol Polymers 0.000 description 2
- 150000003077 polyols Chemical class 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 238000007639 printing Methods 0.000 description 2
- IDHBLVYDNJDWNO-UHFFFAOYSA-N propyl octanoate Chemical compound CCCCCCCC(=O)OCCC IDHBLVYDNJDWNO-UHFFFAOYSA-N 0.000 description 2
- 235000005713 safflower oil Nutrition 0.000 description 2
- 239000003813 safflower oil Substances 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- 159000000000 sodium salts Chemical class 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000003549 soybean oil Substances 0.000 description 2
- 235000012424 soybean oil Nutrition 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- 239000002383 tung oil Substances 0.000 description 2
- 229920006305 unsaturated polyester Polymers 0.000 description 2
- 239000002966 varnish Substances 0.000 description 2
- 235000019871 vegetable fat Nutrition 0.000 description 2
- MUTGBJKUEZFXGO-OLQVQODUSA-N (3as,7ar)-3a,4,5,6,7,7a-hexahydro-2-benzofuran-1,3-dione Chemical compound C1CCC[C@@H]2C(=O)OC(=O)[C@@H]21 MUTGBJKUEZFXGO-OLQVQODUSA-N 0.000 description 1
- 125000001989 1,3-phenylene group Chemical group [H]C1=C([H])C([*:1])=C([H])C([*:2])=C1[H] 0.000 description 1
- SBJCUZQNHOLYMD-UHFFFAOYSA-N 1,5-Naphthalene diisocyanate Chemical compound C1=CC=C2C(N=C=O)=CC=CC2=C1N=C=O SBJCUZQNHOLYMD-UHFFFAOYSA-N 0.000 description 1
- ATOUXIOKEJWULN-UHFFFAOYSA-N 1,6-diisocyanato-2,2,4-trimethylhexane Chemical compound O=C=NCCC(C)CC(C)(C)CN=C=O ATOUXIOKEJWULN-UHFFFAOYSA-N 0.000 description 1
- FAHUKNBUIVOJJR-UHFFFAOYSA-N 1-(4-fluorophenyl)-1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazine Chemical compound C1=CC(F)=CC=C1C1C2=CC=CN2CCN1 FAHUKNBUIVOJJR-UHFFFAOYSA-N 0.000 description 1
- BUZMJVBOGDBMGI-UHFFFAOYSA-N 1-phenylpropylbenzene Chemical compound C=1C=CC=CC=1C(CC)C1=CC=CC=C1 BUZMJVBOGDBMGI-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- GHKSKVKCKMGRDU-UHFFFAOYSA-N 2-(3-aminopropylamino)ethanol Chemical compound NCCCNCCO GHKSKVKCKMGRDU-UHFFFAOYSA-N 0.000 description 1
- IWSZDQRGNFLMJS-UHFFFAOYSA-N 2-(dibutylamino)ethanol Chemical compound CCCCN(CCO)CCCC IWSZDQRGNFLMJS-UHFFFAOYSA-N 0.000 description 1
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
- GTACSIONMHMRPD-UHFFFAOYSA-N 2-[4-[2-(benzenesulfonamido)ethylsulfanyl]-2,6-difluorophenoxy]acetamide Chemical compound C1=C(F)C(OCC(=O)N)=C(F)C=C1SCCNS(=O)(=O)C1=CC=CC=C1 GTACSIONMHMRPD-UHFFFAOYSA-N 0.000 description 1
- GVNHOISKXMSMPX-UHFFFAOYSA-N 2-[butyl(2-hydroxyethyl)amino]ethanol Chemical compound CCCCN(CCO)CCO GVNHOISKXMSMPX-UHFFFAOYSA-N 0.000 description 1
- 125000003006 2-dimethylaminoethyl group Chemical group [H]C([H])([H])N(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical class [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 1
- YZTJKOLMWJNVFH-UHFFFAOYSA-N 2-sulfobenzene-1,3-dicarboxylic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1S(O)(=O)=O YZTJKOLMWJNVFH-UHFFFAOYSA-N 0.000 description 1
- RDFQSFOGKVZWKF-UHFFFAOYSA-N 3-hydroxy-2,2-dimethylpropanoic acid Chemical compound OCC(C)(C)C(O)=O RDFQSFOGKVZWKF-UHFFFAOYSA-N 0.000 description 1
- CTJFNNZDSZIGOM-UHFFFAOYSA-N 3-methylcyclohex-2-ene-1,1,2-tricarboxylic acid Chemical class CC1=C(C(O)=O)C(C(O)=O)(C(O)=O)CCC1 CTJFNNZDSZIGOM-UHFFFAOYSA-N 0.000 description 1
- YHFGMFYKZBWPRW-UHFFFAOYSA-N 3-methylpentane-1,1-diol Chemical compound CCC(C)CC(O)O YHFGMFYKZBWPRW-UHFFFAOYSA-N 0.000 description 1
- 229940090248 4-hydroxybenzoic acid Drugs 0.000 description 1
- KDVYCTOWXSLNNI-UHFFFAOYSA-N 4-t-Butylbenzoic acid Chemical compound CC(C)(C)C1=CC=C(C(O)=O)C=C1 KDVYCTOWXSLNNI-UHFFFAOYSA-N 0.000 description 1
- YCPXWRQRBFJBPZ-UHFFFAOYSA-N 5-sulfosalicylic acid Chemical compound OC(=O)C1=CC(S(O)(=O)=O)=CC=C1O YCPXWRQRBFJBPZ-UHFFFAOYSA-N 0.000 description 1
- 101710130081 Aspergillopepsin-1 Proteins 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N Benzoic acid Natural products OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
- ROFVEXUMMXZLPA-UHFFFAOYSA-N Bipyridyl Chemical group N1=CC=CC=C1C1=CC=CC=N1 ROFVEXUMMXZLPA-UHFFFAOYSA-N 0.000 description 1
- 229930185605 Bisphenol Natural products 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 150000000703 Cerium Chemical class 0.000 description 1
- 102100031007 Cytosolic non-specific dipeptidase Human genes 0.000 description 1
- 240000008415 Lactuca sativa Species 0.000 description 1
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 1
- CJKRXEBLWJVYJD-UHFFFAOYSA-N N,N'-diethylethylenediamine Chemical compound CCNCCNCC CJKRXEBLWJVYJD-UHFFFAOYSA-N 0.000 description 1
- 206010028980 Neoplasm Diseases 0.000 description 1
- 229920000305 Nylon 6,10 Polymers 0.000 description 1
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- UWZVPQKWYFZLLW-UHFFFAOYSA-N Propyl heptanoate Chemical compound CCCCCCC(=O)OCCC UWZVPQKWYFZLLW-UHFFFAOYSA-N 0.000 description 1
- NRCMAYZCPIVABH-UHFFFAOYSA-N Quinacridone Chemical compound N1C2=CC=CC=C2C(=O)C2=C1C=C1C(=O)C3=CC=CC=C3NC1=C2 NRCMAYZCPIVABH-UHFFFAOYSA-N 0.000 description 1
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 238000007605 air drying Methods 0.000 description 1
- 125000005907 alkyl ester group Chemical group 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 238000003556 assay Methods 0.000 description 1
- ONJMNXFNTYIEEA-UHFFFAOYSA-N benzene ethene Chemical compound C1=CC=CC=C1.C=C.C=C.C=C ONJMNXFNTYIEEA-UHFFFAOYSA-N 0.000 description 1
- WXBLLCUINBKULX-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1.OC(=O)C1=CC=CC=C1 WXBLLCUINBKULX-UHFFFAOYSA-N 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 210000000988 bone and bone Anatomy 0.000 description 1
- 230000031709 bromination Effects 0.000 description 1
- 238000005893 bromination reaction Methods 0.000 description 1
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 1
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 1
- 159000000007 calcium salts Chemical class 0.000 description 1
- 201000011510 cancer Diseases 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 238000005660 chlorination reaction Methods 0.000 description 1
- 239000008199 coating composition Substances 0.000 description 1
- 150000001869 cobalt compounds Chemical class 0.000 description 1
- 235000020057 cognac Nutrition 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 description 1
- XLJMAIOERFSOGZ-UHFFFAOYSA-M cyanate Chemical compound [O-]C#N XLJMAIOERFSOGZ-UHFFFAOYSA-M 0.000 description 1
- 239000013530 defoamer Substances 0.000 description 1
- JGFBRKRYDCGYKD-UHFFFAOYSA-N dibutyl(oxo)tin Chemical compound CCCC[Sn](=O)CCCC JGFBRKRYDCGYKD-UHFFFAOYSA-N 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 125000005313 fatty acid group Chemical group 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- JBFHTYHTHYHCDJ-UHFFFAOYSA-N gamma-caprolactone Chemical compound CCC1CCC(=O)O1 JBFHTYHTHYHCDJ-UHFFFAOYSA-N 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 229910052738 indium Inorganic materials 0.000 description 1
- 239000002440 industrial waste Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 1
- 238000005304 joining Methods 0.000 description 1
- 150000002596 lactones Chemical class 0.000 description 1
- 239000011133 lead Substances 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 150000004702 methyl esters Chemical class 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- WHIVNJATOVLWBW-UHFFFAOYSA-N n-butan-2-ylidenehydroxylamine Chemical compound CCC(C)=NO WHIVNJATOVLWBW-UHFFFAOYSA-N 0.000 description 1
- 229940117969 neopentyl glycol Drugs 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- BPYXFMVJXTUYRV-UHFFFAOYSA-J octanoate;zirconium(4+) Chemical class [Zr+4].CCCCCCCC([O-])=O.CCCCCCCC([O-])=O.CCCCCCCC([O-])=O.CCCCCCCC([O-])=O BPYXFMVJXTUYRV-UHFFFAOYSA-J 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 150000002926 oxygen Chemical class 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 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 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000003505 polymerization initiator Substances 0.000 description 1
- 229920006324 polyoxymethylene Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- ULWHHBHJGPPBCO-UHFFFAOYSA-N propane-1,1-diol Chemical class CCC(O)O ULWHHBHJGPPBCO-UHFFFAOYSA-N 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- OVFMRFMJVFDSAA-UHFFFAOYSA-N propyl decanoate Chemical compound CCCCCCCCCC(=O)OCCC OVFMRFMJVFDSAA-UHFFFAOYSA-N 0.000 description 1
- FTBUKOLPOATXGV-UHFFFAOYSA-N propyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OCCC FTBUKOLPOATXGV-UHFFFAOYSA-N 0.000 description 1
- HTUIWRWYYVBCFT-UHFFFAOYSA-N propyl hexanoate Chemical compound CCCCCC(=O)OCCC HTUIWRWYYVBCFT-UHFFFAOYSA-N 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000007665 sagging Methods 0.000 description 1
- 235000012045 salad Nutrition 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000008247 solid mixture Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 229960005137 succinic acid Drugs 0.000 description 1
- 239000003930 superacid Substances 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- PJANXHGTPQOBST-VAWYXSNFSA-N trans-stilbene Chemical group C=1C=CC=CC=1/C=C/C1=CC=CC=C1 PJANXHGTPQOBST-VAWYXSNFSA-N 0.000 description 1
- SRPWOOOHEPICQU-UHFFFAOYSA-N trimellitic anhydride Chemical compound OC(=O)C1=CC=C2C(=O)OC(=O)C2=C1 SRPWOOOHEPICQU-UHFFFAOYSA-N 0.000 description 1
- QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 description 1
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Classifications
-
- 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
- C09D11/00—Inks
- C09D11/30—Inkjet printing inks
-
- 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
- C08K5/09—Carboxylic acids; Metal salts thereof; Anhydrides thereof
- C08K5/098—Metal salts of carboxylic acids
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J27/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
- B01J27/24—Nitrogen compounds
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
- B01J31/04—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing carboxylic acids or their salts
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
- B01J31/12—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing organo-metallic compounds or metal hydrides
- B01J31/128—Mixtures of organometallic compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F120/00—Homopolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride, ester, amide, imide or nitrile thereof
- C08F120/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F120/10—Esters
- C08F120/20—Esters of polyhydric alcohols or polyhydric phenols, e.g. 2-hydroxyethyl (meth)acrylate or glycerol mono-(meth)acrylate
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F242/00—Copolymers of drying oils with other monomers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F283/00—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G
- C08F283/01—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G on to unsaturated polyesters
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F4/00—Polymerisation catalysts
- C08F4/42—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors
- C08F4/72—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from metals not provided for in group C08F4/44
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/24—Crosslinking, e.g. vulcanising, of macromolecules
-
- 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
- C08K5/16—Nitrogen-containing compounds
- C08K5/17—Amines; Quaternary ammonium compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L101/00—Compositions of unspecified macromolecular compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L91/00—Compositions of oils, fats or waxes; Compositions of derivatives thereof
- C08L91/005—Drying oils
-
- 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
- C09D11/00—Inks
- C09D11/02—Printing inks
- C09D11/03—Printing inks characterised by features other than the chemical nature of the binder
-
- 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
- C09D11/00—Inks
- C09D11/02—Printing inks
- C09D11/06—Printing inks based on fatty oils
-
- 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
- C09D11/00—Inks
- C09D11/02—Printing inks
- C09D11/10—Printing inks based on artificial resins
-
- 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
- C09D11/00—Inks
- C09D11/02—Printing inks
- C09D11/10—Printing inks based on artificial resins
- C09D11/102—Printing inks based on artificial resins containing macromolecular compounds obtained by reactions other than those only involving unsaturated carbon-to-carbon bonds
-
- 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
- C09D11/00—Inks
- C09D11/02—Printing inks
- C09D11/10—Printing inks based on artificial resins
- C09D11/102—Printing inks based on artificial resins containing macromolecular compounds obtained by reactions other than those only involving unsaturated carbon-to-carbon bonds
- C09D11/104—Polyesters
- C09D11/105—Alkyd resins
-
- 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
- C09D11/00—Inks
- C09D11/02—Printing inks
- C09D11/10—Printing inks based on artificial resins
- C09D11/106—Printing inks based on artificial resins containing macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C09D11/107—Printing inks based on artificial resins containing macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds from unsaturated acids or derivatives thereof
-
- 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
- C09D167/00—Coating compositions based on polyesters obtained by reactions forming a carboxylic ester link in the main chain; Coating compositions based on derivatives of such polymers
- C09D167/08—Polyesters modified with higher fatty oils or their acids, or with natural resins or resin acids
-
- 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
- C09D191/00—Coating compositions based on oils, fats or waxes; Coating compositions based on derivatives thereof
- C09D191/005—Drying oils
-
- 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
- C09D201/00—Coating compositions based on unspecified macromolecular compounds
- C09D201/02—Coating compositions based on unspecified macromolecular compounds characterised by the presence of specified groups, e.g. terminal or pendant functional groups
-
- 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
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09F—NATURAL RESINS; FRENCH POLISH; DRYING-OILS; OIL DRYING AGENTS, i.e. SICCATIVES; TURPENTINE
- C09F9/00—Compounds to be used as driers, i.e. siccatives
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K3/00—Materials not provided for elsewhere
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2231/00—Catalytic reactions performed with catalysts classified in B01J31/00
- B01J2231/30—Addition reactions at carbon centres, i.e. to either C-C or C-X multiple bonds
- B01J2231/32—Addition reactions to C=C or C-C triple bonds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2410/00—Features related to the catalyst preparation, the catalyst use or to the deactivation of the catalyst
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2810/00—Chemical modification of a polymer
- C08F2810/20—Chemical modification of a polymer leading to a crosslinking, either explicitly or inherently
-
- 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
- C08K2201/00—Specific properties of additives
- C08K2201/014—Additives containing two or more different additives of the same subgroup in C08K
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Polymers & Plastics (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- General Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Paints Or Removers (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
- Polyesters Or Polycarbonates (AREA)
Abstract
本发明的目的在于,提供能够降低钴金属皂的用量、具有与钴金属皂所具有的优异的固化性能同等以上的固化性能的氧化聚合型不饱和树脂用固化促进剂、和使用其的印刷油墨及涂料,提供固化促进剂、包含该固化促进剂的印刷油墨及涂料,所述固化促进剂含有:脂肪酸锰盐(A),下述通式(1)所示的氨基醇(B)(式中,R1及R2分别独立地表示氢原子或碳原子数1~6的烷基,X1及X2分别独立地表示碳原子数2~6的亚烷基,Y表示-NR3-(其中,R3表示氢原子或碳原子数1~6的烷基。)或氧原子。),和选自由脂肪酸铋盐、脂肪酸锆盐、脂肪酸钡盐及脂肪酸铁盐组成的组中的1种以上的脂肪酸的金属盐(C)。
Description
技术领域
本发明涉及氧化聚合型不饱和树脂的固化性优异的固化促进剂、和使用其的印刷油墨和涂料。
背景技术
在使用氧化聚合型树脂作为印刷油墨、涂料等的构成成分的领域中添加催干剂作为用于使该树脂干燥的固化促进剂。作为该油墨中使用的催干剂,通常是钴、锰、铅、铁、锌等重金属与各种羧酸的金属盐(以下有时简记作“金属皂”)。
含有氧化聚合型树脂的涂料等通常在室外进行涂装,因此,要求经过一年在从低温到常温的大气温度下使涂料在短时间内固化、提高室外涂装的操作效率。因此,具有较强的固化促进性的钴、锰等有机酸金属盐主要作为氧化聚合型树脂的固化促进剂(催干剂)来使用。
钴金属皂虽然具有优异的干燥性能,但存在以下问题:若为了进一步缩短干燥时间而大量使用,则印刷油墨、涂料的表面干燥非常迅速地进行,产生结皮而成为皱褶、收缩的原因,很难兼顾快的干燥时间和因结皮而产生的皱褶、收缩的防止。
此外,作为钴金属皂的原料的钴化合物,存在以下两点:在国际癌研究机关的致癌性风险一览中被列在“疑有对人类的致癌性”的组2B中,致癌性令人担忧;由于金属钴为稀少金属,所以供给不稳定,钴金属皂在成本方面昂贵等,要求进一步降低钴金属皂的用量、并且具有高固化性能的固化促进剂。
因此,作为以更少的钴金属皂的用量得到高固化性能的例子,提出了含有钴金属皂、锰金属皂及选自二乙醇胺、二乙基乙醇胺、二丁基乙醇胺、正丁基二乙醇胺中的至少一种氨基醇的固化促进剂(例如参照专利文献1。)。然而,由于依然使用钴金属皂,所以未解决上述的致癌性的担忧、原料的供给不稳定及成本高的问题。
需要说明的是,作为不使用钴金属来防止因该结皮而产生的褶皱、收缩、并且进一步缩短干燥时间的方法,组合使用了锰皂和联吡啶的干燥促进剂(固化促进剂)在前述专利文献1被公开以前已经被提出(例如参照专利文献2。)。然而,专利文献2中记载的干燥促进剂虽然具有完全不使用钴金属皂的优点,但是用作印刷油墨、涂料的固化促进剂时,存在干燥时间变长的问题。
现有技术文献
专利文献
专利文献1:日本特开2001-49102号公报
专利文献2:美国专利第2565897号
发明内容
发明要解决的问题
本发明要解决的课题在于,提供氧化聚合型不饱和树脂用固化促进剂、和使用其的印刷油墨及涂料,所述氧化聚合型不饱和树脂用固化促进剂能够进一步降低担忧对人体造成影响的钴金属皂的用量、具有与钴金属皂所具有的优异的固化性能同等以上的固化性能。
用于解决问题的方案
本发明人等反复进行了深入研究,结果发现:通过组合使用作为脂肪酸金属盐的非钴的脂肪酸锰盐,特定的氨基醇,和选自由脂肪酸铋盐、脂肪酸锆盐、脂肪酸钡盐及脂肪酸铁盐组成的组中的1种以上的脂肪酸的金属盐,可以解决上述课题,从而完成了本发明。
即,本发明提供一种氧化聚合型不饱和树脂用固化促进剂,其特征在于,其含有:
脂肪酸锰盐(A),下述通式(1)所示的氨基醇(B),和选自由脂肪酸铋盐、脂肪酸锆盐、脂肪酸钡盐及脂肪酸铁盐组成的组中的1种以上的脂肪酸的金属盐(C)。
(式(1)中,R1及R2分别独立地表示氢原子或碳原子数1~6的烷基,X1及X2分别独立地表示碳原子数2~6的亚烷基,Y表示-NR3-(其中,R3表示氢原子或碳原子数1~6的烷基)或氧原子。)
另外,本发明提供一种印刷油墨,其特征在于,含有前述氧化聚合型不饱和树脂用固化促进剂和氧化聚合型不饱和树脂。
进而,本发明提供一种涂料,其特征在于,含有前述氧化聚合型不饱和树脂用固化促进剂和氧化聚合型不饱和树脂。
发明的效果
本发明的氧化聚合型不饱和树脂用固化促进剂解决致癌性的担忧、原料的供给不稳定及成本高的问题、并且固化时间短、具有优异的固化性能。因此,可以作为以平版印刷用油墨为代表的酸值聚合干燥型印刷油墨、涂料的固化促进剂适当地利用。
具体实施方式
本发明的氧化聚合型不饱和树脂用固化促进剂含有:
脂肪酸锰盐(A),下述通式(1)所示的氨基醇(B),和选自由脂肪酸铋盐、脂肪酸锆盐、脂肪酸钡盐及脂肪酸铁盐组成的组中的1种以上的脂肪酸的金属盐(C)。
(式(1)中,R1及R2分别独立地表示氢原子或碳原子数1~6的烷基,X1及X2分别独立地表示碳原子数2~6的亚烷基,Y表示-NR3-(其中,R3表示氢原子或碳原子数1~6的烷基)或氧原子。)
前述脂肪酸锰盐(A)是脂肪酸的锰盐,作为前述脂肪酸,可列举出辛酸、环烷酸、新癸酸、异壬酸、桐油酸、亚麻仁油酸、大豆油酸、树脂酸、妥尔油脂肪酸等。这些脂肪酸锰盐(A)可以单独使用,也可以组合使用两种以上。
前述脂肪酸锰盐(A)中,从对作为印刷油墨及涂料的原料使用的溶剂的溶解性良好的理由考虑,优选脂肪酸为选自由辛酸、新癸酸、异壬酸及环烷酸组成的组中的至少1种脂肪酸。
前述脂肪酸锰盐(A)可以通过将脂肪酸制成可溶于水的盐、通常为钠盐溶解于水中,向其中加入可溶于水的锰盐,进行所谓的复分解的离子交换反应,并进行水洗、脱水、过滤而得到。
前述氨基醇(B)为下述通式(1)所示的化合物。本发明中,通过使用该具有下述通式(1)结构的氨基醇,从而印刷油墨、涂料的干燥时间(固化时间)短、能够发挥优异的固化性能。另外,由于油墨、涂料的表面干燥快速地进行,所以还可以防止引起的涂膜表面的褶皱、收缩的发生。
(式(1)中,R1及R2分别独立地表示氢原子或碳原子数1~6的烷基,X1及X2分别独立地表示碳原子数2~6的亚烷基,Y表示-NR3-(其中,R3表示氢原子或碳原子数1~6的烷基)或氧原子。)
前述通式(1)所示的氨基醇(B)中,从进一步缩短固化时间的方面考虑,优选X1及X2分别为碳原子数2~3的亚烷基。通过使用X1及X2分别为碳原子数2~3的亚烷基的氨基醇,还可以防止由油墨、涂料的表面干燥快速地进行而引起的涂膜表面的褶皱、收缩的发生。
作为前述氨基醇(B)的具体例,可以优选举出2-[(2-二甲基氨基乙基)甲基氨基]乙醇、2-(2-氨基乙基)氨基乙醇、1-(2-氨基乙基)氨基-2-丙醇、2-(3-氨基丙基氨基)乙醇、2-(2-二甲基氨基乙氧基)乙醇。需要说明的是,这些氨基醇(B)可以单独使用,也可以组合使用2种以上。
为了进一步提高固化性能,前述脂肪酸锰盐(A)中的锰金属与前述氨基醇(B)的以质量基准计的配混比(A)/(B)优选为1/0.1~1/30的范围,更优选为1/0.3~1/20的范围,进一步优选为1/0.5~1/10的范围。
本发明中使用的脂肪酸的金属盐(C)选自由脂肪酸铋盐、脂肪酸锆盐、脂肪酸钡盐及脂肪酸铁盐组成的组。氧化聚合型不饱和树脂被空气中的氧氧化而不饱和键发生聚合并固化。通常,含有脂肪酸锰盐的固化促进剂的脂肪酸锰盐摄取空气中的氧,利用该氧使氧化聚合型不饱和树脂固化。本发明中,发明人等认为,脂肪酸的金属盐(C)由于促进脂肪酸锰盐(A)的空气中的氧的摄取所以提高氧化聚合型不饱和树脂的固化性。
脂肪酸铋盐为脂肪酸的铋盐,作为前述脂肪酸,可以举出辛酸、环烷酸、新癸酸、异壬酸、桐油酸、亚麻仁油酸、大豆油酸、树脂酸、妥尔油脂肪酸等。
脂肪酸锆盐为脂肪酸的锆盐,作为前述脂肪酸,可以举出辛酸、环烷酸、新癸酸、异壬酸、桐油酸、亚麻仁油酸、大豆油酸、树脂酸、妥尔油脂肪酸等。
脂肪酸钡盐为脂肪酸的钡盐,作为前述脂肪酸,可以举出辛酸、环烷酸、新癸酸、异壬酸、桐油酸、亚麻仁油酸、大豆油酸、树脂酸、妥尔油脂肪酸等。
脂肪酸铁盐为脂肪酸的铁盐,作为前述脂肪酸,可以举出辛酸、环烷酸、新癸酸、异壬酸、桐油酸、亚麻仁油酸、大豆油酸、树脂酸、妥尔油脂肪酸等。
氧化聚合型不饱和树脂用固化促进剂中的脂肪酸的金属盐(C)的含量根据使用的脂肪酸的金属盐的种类而适当改变,因此可以将氧化聚合型不饱和树脂的固化性最大限度地提高。例如使用选自由脂肪酸铋盐、脂肪酸锆盐及脂肪酸钡盐组成的组中的1种以上的脂肪酸的金属盐(C1)作为脂肪酸的金属盐(C)时,相对于脂肪酸锰盐(A)中的锰金属1质量份,优选以金属盐(C1)中的金属的量为1~10质量份的方式含有金属盐(C1),更优选以金属盐(C1)中的金属的量为3~7质量份的方式含有金属盐(C1)。
另外,使用脂肪酸铁盐(C2)作为脂肪酸的金属盐(C)时,相对于脂肪酸锰盐(A)中的锰金属1质量份,优选以脂肪酸铁盐(C2)中的金属的量为0.1~2.0质量份的方式含有金属盐(C2),更优选以金属盐(C2)中的金属的量为0.2~1质量份的方式含有金属盐(C2)。
在不破坏本发明的效果的范围内,也可以在本发明的氧化聚合型不饱和树脂用固化促进剂中添加除前述脂肪酸锰盐(A)、脂肪酸的金属盐(C)以外的脂肪酸的金属盐。作为这样的脂肪酸的金属盐,例如可以举出脂肪酸镍盐、脂肪酸铜盐、脂肪酸锌盐、脂肪酸铈盐、脂肪酸钒盐、脂肪酸钙盐及脂肪酸锶盐等。其中,从可以得到氧化聚合型不饱和树脂的涂膜的指触干燥性优异的固化促进剂的方面考虑,优选脂肪酸钙盐或脂肪酸锶盐(D),更优选为脂肪酸钙盐。
作为前述脂肪酸钙盐或脂肪酸锶盐(D)的用量,优选相对于脂肪酸锰盐(A)中的锰金属1质量份,脂肪酸钙或锶盐(D)中的金属的量为1~5质量份的量。
需要说明的是,前述脂肪酸铋盐可以使用以市售品的形式被销售的产品,也可以根据需要制造。为了制造脂肪酸铋盐,可以通过例如在前述的脂肪酸中加入铋、或它们的水合物、氢氧化物、碳酸盐等铋化合物,然后在高温的气氛化中搅拌使其反应而得到。反应时的温度通常为40℃~200℃,优选为80℃~150℃。另外,反应的时间通常为1~10小时,优选为1~5小时。此处使用的脂肪酸和铋或铋化合物的摩尔比(脂肪酸/铋或铋化合物的摩尔比)通常为2.0~4.0的范围,优选为2.5~3.5的范围。
本发明的氧化聚合型不饱和树脂用固化促进剂优选通过将前述脂肪酸锰盐(A)及前述氨基醇(B)及脂肪酸的金属盐(C)用稀释剂(E)稀释,从而作为处理性良好的溶液使用。作为前述稀释剂,例如可举出甲苯、二甲苯、庚烷、己烷、矿物油精(mineralspirit)等烃系溶剂;甲醇、乙醇、丙醇、环己醇等醇系溶剂;甲乙酮、甲基异丁基酮、环己酮等酮系溶剂;丙醚、甲基溶纤剂、溶纤剂、丁基溶纤剂、甲基卡必醇等醚系溶剂;己酸甲酯、癸酸甲酯、月桂酸甲酯等脂肪酸酯;大豆油、亚麻仁油、菜籽油、红花油等植物油脂;下述通式(2)所示的脂肪酸酯(E1)等,这些稀释剂可以仅使用1种也可以组合使用2种以上。
(式(2)中,R4为碳原子数5~11的烷基,R5为碳原子数1~3的烷基。)
前述脂肪酸酯(E1)是通过使碳原子数6~12的羧酸和碳原子数1~3的醇发生酯化反应而得到的,前述羧酸及醇的碳链可以为直链状也可以为支链状。
作为前述脂肪酸酯(E1),例如可以举出己酸甲酯、庚酸甲酯、辛酸甲酯、壬酸甲酯、癸酸甲酯、月桂酸甲酯、己酸乙酯、庚酸乙酯、辛酸乙酯、壬酸乙酯、癸酸乙酯、月桂酸乙酯、己酸丙酯、庚酸丙酯、辛酸丙酯、壬酸丙酯、癸酸丙酯、月桂酸丙酯等。这些脂肪酸酯可以单独使用也可以组合使用2种以上。另外,这些脂肪酸酯中,己酸甲酯、癸酸甲酯、月桂酸甲酯由于臭气少所以优选。特别是月桂酸甲酯由于可以同时实现印刷油墨用催干剂的粘度降低和臭气的降低,故优选。
另外,为了制成粘度更低且处理性优异的固化促进剂,前述脂肪酸锰盐(A)、氨基醇(B)及脂肪酸的金属盐(C)的总量与前述稀释剂(E)的以质量基准计的配混比[(A)+(B)+(C)]/(E)优选为10/90~95/5的范围,更优选为40/60~80/20的范围,进一步优选为20/80~90/10的范围。
本发明的印刷油墨是将本发明的氧化聚合型不饱和树脂用固化促进剂、氧化聚合型不饱和树脂和着色剂配混而得到的。通常,印刷油墨由作为粘合剂树脂的清漆(氧化聚合型不饱和树脂的溶剂溶液)、作为颜料或染料的着色剂、用于调节印刷油墨粘度及干燥性的稀释剂形成。作为清漆中使用的氧化聚合型不饱和树脂,例如可以举出松香改性酚醛树脂、马来酸改性酚醛树脂、不饱和聚酯、石油树脂、醇酸树脂等。
另外,作为着色剂,可列举出炭黑、酞菁颜料、氧化铁红(Bengala)、偶氮颜料、喹吖啶酮颜料等。进而,作为稀释剂,例如可列举出甲苯、二甲苯、庚烷、己烷、矿物油精等烃系溶剂;甲醇、乙醇、丙醇、环己醇等醇系溶剂;甲乙酮、甲基异丁基酮、环己酮等酮系溶剂;丙醚、甲基溶纤剂、溶纤剂、丁基溶纤剂、甲基卡必醇等醚系溶剂;己酸甲酯、癸酸甲酯、月桂酸甲酯等脂肪酸酯;大豆油、亚麻仁油、菜籽油、红花油等植物油脂等。
作为本发明的印刷油墨的制造方法,可列举出将前述清漆、着色剂、稀释溶剂、本发明的氧化聚合型不饱和树脂用固化促进剂、以及根据需要而使用的蜡等其它添加剂用三辊式研墨辊等研墨机进行研墨的方法。此时,本发明的印刷油墨用催干剂优选使用以所述脂肪酸酯(E1)或植物油脂稀释而得到的物质。
关于本发明的氧化聚合型不饱和树脂用固化促进剂在印刷油墨中的配混量,从能够兼顾短干燥时间和防止结皮的方面出发,相对于印刷油墨中的清漆100质量份,换算成锰原子,优选为0.001~1质量份的范围,更优选为0.01~0.5质量份的范围。
本发明的涂料的特征在于,含有本发明的氧化聚合型不饱和树脂用固化促进剂和氧化聚合型不饱和树脂。
作为前述氧化聚合型不饱和树脂,例如可以举出氧化聚合固化型醇酸树脂、氧化聚合固化型聚氨酯树脂、氧化聚合固化型改性环氧树脂等。
作为上述氧化聚合固化型醇酸树脂,可以举出以多元酸成分、多元醇成分及油脂肪酸作为主要原料成分的酯系树脂。
作为上述多元酸成分,例如可以主要使用邻苯二甲酸酐、间苯二甲酸、对苯二甲酸、四氢邻苯二甲酸酐、六氢邻苯二甲酸酐、琥珀酸、富马酸、己二酸、癸二酸、马来酸酐等二元酸;及这些酸的低级烷基酯化物。进而可以根据需要使用偏苯三酸酐、甲基环己烯三羧酸、均苯四酸酐等3元以上的多元酸;磺基邻苯二甲酸、磺基间苯二甲酸及它们的铵盐、钠盐、低级烷基酯化物等。另外,作为酸成分,为了分子量调整等目的,可以组合使用苯甲酸、巴豆酸、对叔丁基苯甲酸等一元酸。
作为前述多元醇成分,例如可以举出乙二醇、二乙二醇、丙二醇、1,4-丁二醇、新戊二醇、3-甲基戊二醇、1,4-己二醇、1,6-己二醇等二元醇。也可以进一步根据需组合使用要甘油、三羟甲基乙烷、三羟甲基丙烷、季戊四醇等3元以上的多元醇;具有聚氧乙烯基的多元醇等。这些多元醇可以单独使用、或混合2种以上进行使用。另外,可以将前述酸成分、醇成分的一部分取代为二羟甲基丙酸、羟基叔戊酸、对羟基苯甲酸等;这些酸的低级烷基酯;ε-己内酯等内酯类等含氧酸成分。
作为前述油脂肪酸,例如可以举出椰子油脂肪酸、大豆油脂肪酸、亚麻仁油脂肪酸、红花油脂肪酸、妥尔油脂肪酸、脱水蓖麻油脂肪酸、桐油脂肪酸等。醇酸树脂的油长(树脂固体成分中的油脂的重量)为5~80质量%、特别是为20~70质量%的范围内时,从所得涂膜的固化性、强靭性、具有肉感等方面考虑,是适宜的。
另外,也可以使用如下树脂:使用环氧化合物作为醇成分的一部分、将环氧化合物部分酯化得到的环氧改性醇酸树脂;在醇酸树脂中引入马来酸酐而得到的马来化醇酸树脂;将马来化醇酸树脂和含羟基醇酸树脂加成而得到的接枝化醇酸树脂;在醇酸树脂上接枝聚合了苯乙烯、(甲基)丙烯酸酯等乙烯基单体而得到的乙烯基改性醇酸树脂等。
进而,也可以使用下述树脂:利用聚酯树脂(以下简称作“再生PES”),使该再生PES溶解在上述醇成分和多元酸成分的混合物中,进行解聚,同时使其进行酯化反应而得到的醇酸树脂、使该醇酸树脂与马来酸酐反应而得到的马来化醇酸树脂、使该醇酸树脂和不具有烯属不饱和基团的酸酐反应而得到的改性醇酸树脂等,所述聚酯树脂是为了资源的再利用而回收的聚对苯二甲酸乙二醇酯(例如PET瓶)、产业废弃物聚对苯二甲酸乙二醇酯、由以对苯二甲酸为主要原料的聚对苯二甲酸乙二醇酯、聚对苯二甲酸丁二醇酯等的聚酯制品(薄膜、纤维、汽车部件、电子部件等)制造时产生的屑等再生的以对苯二甲酸为主要原料的聚酯树脂。
从固化性及涂膜物性良好的方面考虑,以上详细描述的氧化聚合固化型醇酸树脂的加德纳粘度(Gardnerviscosity)(25℃)优选为15~60斯托克斯。
作为前述聚氨酯树脂,没有特别限定,例如可以使用使多元醇、油脂和多元醇经过再酯化得到的多元醇、与多异氰酸酯反应而得到的聚氨酯树脂。
作为上述多异氰酸酯,例如可以举出1,4-四亚甲基二异氰酸酯、1,6-六亚甲基二异氰酸酯、2,2,4-三甲基六亚甲基二异氰酸酯、2,8-二异氰酸酯甲基己酸酯等脂肪族异氰酸酯类;3-异氰酸酯甲基-3,5,5-三甲基环己基异氰酸酯、甲基环己基-2,4-二异氰酸酯等脂环族二异氰酸酯类;甲代亚苯基二异氰酸酯、二苯基甲烷二异氰酸酯、1,5-萘二异氰酸酯、二苯基甲基甲烷二异氰酸酯、四烷基二苯基甲烷二异氰酸酯、4,4-二苄基二异氰酸酯、1,3-亚苯基二异氰酸酯等芳香族二异氰酸酯类;氯化二异氰酸酯类、溴化二异氰酸酯类等,它们可以单独使用或以2种以上的混合物的形式来使用。
作为前述多元醇,可以举出通常聚氨酯树脂的制造中使用的各种多元醇、例如二乙二醇、丁二醇、己二醇、新戊二醇、双酚A、环己烷二甲醇、三羟甲基丙烷、甘油、季戊四醇、聚乙二醇、聚丙二醇、聚酯多元醇、聚己内酯、聚四亚甲基醚二醇、聚硫醚多元醇、聚缩醛多元醇、聚丁二烯多元醇、呋喃二甲醇等,它们可以单独使用或以2种以上的混合物的形式来使用。
作为前述油脂和多元醇经过酯化而得到的多元醇,例如可以举出将碘值为7~200的油脂和三羟甲基丙烷、季戊四醇等多元醇酯化而得到的多元醇,也可以使用例如三井化学株式会社制造“XP1076E”、“XP1077E”、“XP1580E”、”FB20-50XB”等市售品。
作为前述氧化聚合固化型改性环氧树脂,例如可以举出以环氧树脂、不饱和脂肪酸成分和含酸基丙烯酸类成分作为原料、使它们进行反应而得到的树脂。关于树脂原料配方,相对于原料的总重量100重量%,环氧树脂为30~50重量%、不饱和脂肪酸成分为25~40重量%及含酸基丙烯酸类成分为10~45重量%时从固化涂膜的物性优选的方面考虑为优选。
另外,氧化聚合固化型改性环氧树脂的碘值从可以得到良好的固化性的方面考虑,优选为30~100,特别优选为35~90。
作为能够用作原料的环氧树脂,没有特别限定,从容易改性、且所得固化涂膜的性能优异的方面考虑,优选双酚A型环氧树脂、氢化双酚A型环氧树脂、双酚F型环氧树脂等双酚型环氧树脂。它们可以单独使用或组合使用2种以上。
作为不饱和脂肪酸成分,天然或合成系的不饱和脂肪酸均可使用,可以使用例如由桐油、亚麻仁油、蓖麻油、脱水蓖麻油、红花油、妥尔油、大豆油、椰子油得到的不饱和脂肪酸等。
另外,作为含酸基丙烯酸类成分,可以使用例如(甲基)丙烯酸和苯乙烯、(甲基)丙烯酸酯类等不含酸基的丙烯酸类单体的混合物等。作为后者不含酸基的丙烯酸类单体,从可以得到优异的涂膜硬度的方面考虑,优选苯乙烯。
氧化聚合固化型改性环氧树脂可以如下所述地得到。首先,由环氧树脂和不饱和脂肪酸成分制造环氧酯树脂。例如将环氧树脂和不饱和脂肪酸成分在甲苯、二甲苯等适当的溶剂中,使用缩合催化剂,根据需要在氮气等非活性气体气氛下、于150~250℃,使其反应直至达到所期望的酸值,由此得到环氧酯树脂。作为缩合催化剂,可以使用例如二丁基氧化锡、四正丁基氯化铵等。
接着,使所得环氧酯树脂与前述含酸基丙烯酸类成分反应,得到氧化聚合固化型改性环氧树脂。环氧酯树脂与含酸基丙烯酸类成分的反应可以在聚合引发剂的存在下、在氮气等非活性气体气氛下、于80~150℃的温度范围内来进行。作为聚合引发剂,可以使用过氧化物、偶氮化合物等各种物质,例如可以以相对于使用的单体总量为0.1~20质量份%的比例使用KayakuakzoCorporation制造“KayabutylB(烷基过酸酯系)”等。
以上详细描述的氧化聚合型不饱和树脂中,本发明中从廉价、容易购买、且涂料的干燥性(实用性)优异的方面考虑,特别优选氧化聚合固化型醇酸树脂。
本发明的涂料优选进一步含有有机溶剂。作为此处能够使用的有机溶剂,例如可以举出前述烃系溶剂、醇系溶剂、酮系溶剂、醚系溶剂。
本发明的涂料在上述各成分的基础上,根据需要还可以含有颜料等色料;颜料分散剂、表面调整剂、紫外线吸收剂、消泡剂、增粘剂、防沉降剂等各种涂料用添加剂。
对本发明催干剂相对于前述涂料的配混量没有特别限定,优选相对于氧化聚合型不饱和树脂100质量份,金属成分的总质量为0.005~1.5质量份的范围。
以上详细描述的本发明的涂料可以通过利用常规方法涂布于被涂物、并干燥/固化从而得到本发明的涂膜。此处,作为能够涂覆本发明的涂料的基材(被涂物),例如可以举出铁钢等。另外,作为涂布后的干燥条件(固化条件),可以举出常温干燥。进而,即使加厚涂膜,本发明的涂料也可以体现出优异的固化性,因此作为厚涂用涂料特别有用,具体而言,可以将固化涂膜的膜厚设为1~500μm的范围。因此,本发明的涂料作为建筑用涂料是有用的。
实施例
以下举出具体的例子,更详细地说明本发明。例子中,只要没有特别说明,“份”、“%”为质量基准。
实施例1~9(氧化聚合型不饱和树脂用固化促进剂的制备)
以第1表及第2表所示的比例(质量份)将脂肪酸锰盐(A)、氨基醇(B)、脂肪酸的金属盐(C)、稀释剂(E)配混,得到本发明的氧化聚合型不饱和树脂用固化促进剂1~9。
[表1]
[表2]
比较例1(同上)
使环烷酸锰56份及2,2’-联吡啶18份溶解于矿物油精26份中,得到比较对照用氧化聚合型不饱和树脂用固化促进剂1′。
比较例2(同上)
使环烷酸钴26份、环烷酸锰21份及二乙醇胺7份溶解于矿物油精46份中,得到比较对照用氧化聚合型不饱和树脂用固化促进剂2′。
比较例3
使环烷酸钴19份及辛酸锆31份溶解于矿物油精50份中,得到比较对照用氧化聚合型不饱和树脂用固化促进剂3′。该固化促进剂是以显示出包括钴金属皂的现有技术的金属皂的平均水准的性能的目的而制作的。
实施例10(涂料的制备)
在将钛白颜料(Tayca株式会社制造“JR-701”)1960、涂料用树脂“BECKOSOLP-470-70”(DIC株式会社制造的、分子内具有氧化聚合型不饱和脂肪酸基团的醇酸系树脂)3340g、矿物油精280g、防结皮剂(甲乙酮肟)20g用三辊磨混炼得到的混合物40g中以锰金属成分相对于树脂不挥发成分100份的比例为0.06%的方式添加氧化聚合型不饱和树脂用固化促进剂1,制备本发明的涂料1。按照下述方法评价涂料1的干燥时间的测定。将评价结果示于第3表。
<干燥时间的测定方法>
使用3密耳的涂敷器(applicator)将涂料涂敷到玻璃板上后,使用干燥时间记录器(太佑机材株式会社制“型号No.404”)进行试验。测定在恒温恒湿室(气温25℃、相对湿度50%)内进行。需要说明的是,涂料的干燥时间设定为:在玻璃板上涂布涂料后,利用干燥时间记录器的针刮出的、涂料开始干燥时可见的刮痕因涂料完全干燥而变得不可见为止的时间。
实施例11~18(同上)
除使用第1表及第2表所示的氧化聚合型不饱和树脂用固化促进剂之外,与实施例10同样地得到涂料2~9。与实施例10同样地测定干燥时间,将其结果示于第3表及第4表。
[表3]
[表4]
比较例4
以锰金属成分相对于树脂不挥发成分100份的比例为0.06%的方式添加氧化聚合型不饱和树脂用固化促进剂1′来代替使用氧化聚合型不饱和树脂用固化促进剂1,除此之外,与实施例10同样地得到比较对照用涂料1′。与实施例10同样地测定干燥时间,将其结果示于第5表。
比较例5
以钴金属成分相对于树脂不挥发成分100份的比例为0.04%的方式添加氧化聚合型不饱和树脂用固化促进剂2′来代替使用氧化聚合型不饱和树脂用固化促进剂1,除此之外,与实施例10同样地得到比较对照用涂料2′。与实施例10同样地测定干燥时间,将其结果示于第5表。
比较例6
以钴金属成分相对于树脂不挥发成分100份的比例为0.06%的方式添加氧化聚合型不饱和树脂用固化促进剂3′来代替使用氧化聚合型不饱和树脂用固化促进剂1,除此之外,与实施例10同样地得到比较对照用涂料3′。与实施例10同样地测定干燥时间,将其结果示于第5表。
[表5]
实施例19
将辛酸锰9份、辛酸铋25份、辛酸钙15份、2-[(2-二甲基氨基乙基)甲基氨基]乙醇2份、矿物油精42份及大豆油(日清奥利友集团株式会社制造“大豆色拉油(S)”)7份混合,得到本发明的氧化聚合型不饱和树脂用固化促进剂10。
实施例20及21
除使用氧化聚合型不饱和树脂用固化促进剂10来代替氧化聚合型不饱和树脂用固化促进剂1之外,与实施例10同样地得到涂料10。与实施例1同样地测定干燥时间,并且按照下述方法进行指触干燥性(粘性)的评价。将其结果示于第4表。另外,作为实施例21,对于涂料1也进行指触干燥性的评价,将其结果一并示于第6表。
<指触干燥性的评价方法>
使用3密耳的涂敷器将涂料涂敷到玻璃板上,形成涂膜后,用指尖轻触涂膜面的中央,测定从涂膜形成时直至指尖不被污染的状态为止的时间(指触干燥时间)。该时间越短,为指触干燥性越优异的涂料。需要说明的是,指触干燥性的评价在恒温恒湿室(气温25℃、相对湿度50%)内进行。[表6]
Claims (9)
1.一种氧化聚合型不饱和树脂用固化促进剂,其特征在于,其含有:
脂肪酸锰盐(A),下述通式(1)所示的氨基醇(B),和选自由脂肪酸铋盐、脂肪酸锆盐、脂肪酸钡盐及脂肪酸铁盐组成的组中的1种以上的脂肪酸的金属盐(C),所述脂肪酸的金属盐(C)的脂肪酸包含选自辛酸、环烷酸、新癸酸、异壬酸、桐油酸、亚麻仁油酸、大豆油酸、树脂酸、妥尔油脂肪酸中的至少一种脂肪酸,
式(1)中,R1及R2分别独立地表示氢原子或碳原子数1~6的烷基,X1及X2分别独立地表示碳原子数2~6的亚烷基,Y表示-NR3-或氧原子,其中,R3表示氢原子或碳原子数1~6的烷基。
2.根据权利要求1所述的氧化聚合型不饱和树脂用固化促进剂,其中,所述脂肪酸的金属盐(C)为选自由脂肪酸铋盐、脂肪酸锆盐及脂肪酸钡盐组成的组中的1种以上的脂肪酸的金属盐(C1),相对于脂肪酸锰盐(A)中的锰金属1质量份,以金属盐(C1)中的金属的量为1~10质量份的方式含有金属盐(C1)。
3.根据权利要求1所述的氧化聚合型不饱和树脂用固化促进剂,其中,所述脂肪酸的金属盐(C)为脂肪酸铁盐(C2),相对于脂肪酸锰盐(A)中的锰金属1质量份,以脂肪酸铁盐(C2)中的金属的量为0.1~2.0质量份的方式含有金属盐(C2)。
4.根据权利要求1所述的氧化聚合型不饱和树脂用固化促进剂,其中,所述氨基醇(B)为选自由2-[(2-二甲基氨基乙基)甲基氨基]乙醇、2-(2-氨基乙基)氨基乙醇、1-(2-氨基乙基)氨基-2-丙醇、2-(3-氨基丙基氨基)乙醇及2-(2-二甲基氨基乙氧基)乙醇组成的组中的至少1种。
5.根据权利要求1所述的氧化聚合型不饱和树脂用固化促进剂,其中,所述脂肪酸锰盐(A)的脂肪酸为选自由辛酸、新癸酸、异壬酸及环烷酸组成的组中的至少1种脂肪酸。
6.根据权利要求1所述的氧化聚合型不饱和树脂用固化促进剂,其中,所述脂肪酸的金属盐(C)的脂肪酸为选自由辛酸、新癸酸及环烷酸组成的组中的至少1种脂肪酸。
7.根据权利要求2或3所述的氧化聚合型不饱和树脂用固化促进剂,其进一步含有脂肪酸钙盐或脂肪酸锶盐。
8.一种印刷油墨,其特征在于,含有权利要求1~7中任一项所述的氧化聚合型不饱和树脂用固化促进剂和氧化聚合型不饱和树脂。
9.一种涂料,其特征在于,含有权利要求1~7中任一项所述的氧化聚合型不饱和树脂用固化促进剂和氧化聚合型不饱和树脂。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2011254975 | 2011-11-22 | ||
JP2011-254975 | 2011-11-22 | ||
PCT/JP2012/079788 WO2013077267A1 (ja) | 2011-11-22 | 2012-11-16 | 酸化重合型不飽和樹脂用硬化促進剤、印刷インキ及び塗料 |
Publications (2)
Publication Number | Publication Date |
---|---|
CN103946317A CN103946317A (zh) | 2014-07-23 |
CN103946317B true CN103946317B (zh) | 2016-05-04 |
Family
ID=48469712
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201280057560.XA Active CN103946317B (zh) | 2011-11-22 | 2012-11-16 | 氧化聚合型不饱和树脂用固化促进剂、印刷油墨及涂料 |
Country Status (7)
Country | Link |
---|---|
US (1) | US9045658B2 (zh) |
EP (1) | EP2784130B1 (zh) |
JP (1) | JP5348515B1 (zh) |
KR (1) | KR101556224B1 (zh) |
CN (1) | CN103946317B (zh) |
TW (1) | TWI542619B (zh) |
WO (1) | WO2013077267A1 (zh) |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2015005121A1 (ja) * | 2013-07-08 | 2015-01-15 | Dic株式会社 | 酸化重合型不飽和樹脂用硬化促進剤、印刷インキ及び塗料 |
FR3021661B1 (fr) * | 2014-05-28 | 2017-12-08 | Eiffage Travaux Publics | Utilisation d'au moins un nucleophile comme accelerateur de siccativation, dans une composition durcissable comprenant au moins une huile vegetale ou animale et au moins un siccatif |
WO2016168319A1 (en) * | 2015-04-13 | 2016-10-20 | University Of South Florida | Cutin-like materials with advanced functionalities and methods of manufacture |
JP6150032B1 (ja) * | 2015-09-08 | 2017-06-21 | Dic株式会社 | 酸化重合型不飽和樹脂用硬化促進剤、印刷インキ及び塗料 |
WO2017067979A1 (en) * | 2015-10-20 | 2017-04-27 | Innovaciones Técnicas Aplicadas A Cerámicas Avanzadas, S.A.U. | Red oil-based inkjet ink comprising iron oxide pigments |
EP3296372B1 (de) * | 2016-09-19 | 2020-03-04 | Daw Se | Lösemittelhaltige beschichtungsmasse |
CN110225932B (zh) * | 2017-01-25 | 2021-11-19 | Dic株式会社 | 活性能量射线固化型水性树脂组合物及无机材料薄膜用底涂剂 |
CN109970993A (zh) * | 2019-04-10 | 2019-07-05 | 烟台大学 | 一种树脂混凝土排水管用不饱和树脂催化剂 |
JP2023061040A (ja) | 2021-10-19 | 2023-05-01 | Dic株式会社 | 酸化重合型不飽和樹脂用硬化促進剤および硬化性樹脂組成物 |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0731136A2 (en) * | 1995-03-07 | 1996-09-11 | Kyowa Chemical Industry Co., Ltd. | Low-temperature-resistant halogen-free, flame-retardant polyolefin-based resin composition |
JP2005154628A (ja) * | 2003-11-27 | 2005-06-16 | Dainippon Ink & Chem Inc | 硬化性樹脂組成物およびそれを含有する印刷インキ |
CN102939349A (zh) * | 2010-06-14 | 2013-02-20 | Dic株式会社 | 印刷油墨用催干剂及使用其的印刷油墨 |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2565897A (en) | 1951-08-28 | Drier compositions | ||
BR9105449A (pt) * | 1990-12-11 | 1992-08-25 | Dow Chemical Co | Composicao para preparar um artigo polimerico espumado moldado e processo para a compatibilizacao de um polial de peso molecular relativamente alto |
JP2001049102A (ja) | 1999-06-03 | 2001-02-20 | Dainippon Ink & Chem Inc | 硬化促進剤及び樹脂組成物 |
KR100596698B1 (ko) * | 1999-06-03 | 2006-07-03 | 다이니혼 잉키 가가쿠 고교 가부시키가이샤 | 경화 촉진제 및 수지 조성물 |
JP5260332B2 (ja) * | 2009-01-16 | 2013-08-14 | 株式会社カネカ | 透明な硬化性組成物および、その硬化物 |
-
2012
- 2012-11-16 US US14/359,390 patent/US9045658B2/en active Active
- 2012-11-16 KR KR1020147011937A patent/KR101556224B1/ko active IP Right Grant
- 2012-11-16 CN CN201280057560.XA patent/CN103946317B/zh active Active
- 2012-11-16 JP JP2013519885A patent/JP5348515B1/ja active Active
- 2012-11-16 EP EP12851247.2A patent/EP2784130B1/en active Active
- 2012-11-16 WO PCT/JP2012/079788 patent/WO2013077267A1/ja active Application Filing
- 2012-11-21 TW TW101143427A patent/TWI542619B/zh active
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0731136A2 (en) * | 1995-03-07 | 1996-09-11 | Kyowa Chemical Industry Co., Ltd. | Low-temperature-resistant halogen-free, flame-retardant polyolefin-based resin composition |
JP2005154628A (ja) * | 2003-11-27 | 2005-06-16 | Dainippon Ink & Chem Inc | 硬化性樹脂組成物およびそれを含有する印刷インキ |
CN102939349A (zh) * | 2010-06-14 | 2013-02-20 | Dic株式会社 | 印刷油墨用催干剂及使用其的印刷油墨 |
Also Published As
Publication number | Publication date |
---|---|
WO2013077267A1 (ja) | 2013-05-30 |
JP5348515B1 (ja) | 2013-11-20 |
CN103946317A (zh) | 2014-07-23 |
EP2784130B1 (en) | 2018-01-10 |
EP2784130A1 (en) | 2014-10-01 |
TW201329144A (zh) | 2013-07-16 |
JPWO2013077267A1 (ja) | 2015-04-27 |
TWI542619B (zh) | 2016-07-21 |
US20140323646A1 (en) | 2014-10-30 |
KR101556224B1 (ko) | 2015-09-30 |
KR20140077947A (ko) | 2014-06-24 |
US9045658B2 (en) | 2015-06-02 |
EP2784130A4 (en) | 2015-06-24 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN103946317B (zh) | 氧化聚合型不饱和树脂用固化促进剂、印刷油墨及涂料 | |
CN102834473B (zh) | 作为用于涂料组合物的干燥剂的锰盐络合物 | |
RU2721703C2 (ru) | Rma-сшиваемые композиции и rma-сшиваемые смолы для получения покрытий, легко поддающихся очистке | |
Ang et al. | Novel approach to convert non-self drying palm stearin alkyds into environmental friendly UV curable resins | |
CN103998544B (zh) | 用于可自氧化的涂料组合物的干燥剂 | |
CN103998545B (zh) | 用于可自氧化的涂料组合物的干燥剂 | |
US20130197152A1 (en) | Polyester resins based on fatty acids that have a short oil length, aqueous dispersions and associated coatings | |
JP2008533290A (ja) | 樹脂、低温配合物、およびそれに由来するコーティング | |
CN101189310A (zh) | 含水涂料组合物 | |
CN1729262A (zh) | 自交联的水性乙酰乙酸酯官能化的磺化醇酸树脂*** | |
WO2013084824A1 (ja) | 塗料用ドライヤー及びそれを用いた塗料 | |
JP5418729B2 (ja) | 印刷インキ及び塗料 | |
US20220275242A1 (en) | A coating composition | |
JPH02235921A (ja) | 塗料用アルキド樹脂 | |
JP2010180299A (ja) | 酸化重合硬化型塗料用ドライヤー、塗料、及びその塗膜 | |
JPS63367A (ja) | 熱硬化性被覆用樹脂組成物 | |
JP2010235644A (ja) | 酸化重合硬化型塗料用ドライヤー、塗料、及びその塗膜 | |
TW201335299A (zh) | 用於可自氧化之塗料組合物之乾燥劑 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C14 | Grant of patent or utility model | ||
GR01 | Patent grant |