TWI628197B - 固化自由基可固化樹脂之方法 - Google Patents
固化自由基可固化樹脂之方法 Download PDFInfo
- Publication number
- TWI628197B TWI628197B TW103143527A TW103143527A TWI628197B TW I628197 B TWI628197 B TW I628197B TW 103143527 A TW103143527 A TW 103143527A TW 103143527 A TW103143527 A TW 103143527A TW I628197 B TWI628197 B TW I628197B
- Authority
- TW
- Taiwan
- Prior art keywords
- metal
- group
- resin
- peroxide
- component
- Prior art date
Links
- 229920005989 resin Polymers 0.000 title claims abstract description 77
- 239000011347 resin Substances 0.000 title claims abstract description 77
- 238000000034 method Methods 0.000 title claims abstract description 19
- 229910052751 metal Inorganic materials 0.000 claims abstract description 30
- 239000002184 metal Substances 0.000 claims abstract description 30
- 229920005588 metal-containing polymer Polymers 0.000 claims abstract description 14
- 229910052802 copper Inorganic materials 0.000 claims abstract description 11
- 229910052742 iron Inorganic materials 0.000 claims abstract description 11
- 125000000524 functional group Chemical group 0.000 claims abstract description 10
- 229910052720 vanadium Inorganic materials 0.000 claims abstract description 10
- 229910052748 manganese Inorganic materials 0.000 claims abstract description 7
- 150000001451 organic peroxides Chemical class 0.000 claims abstract description 7
- 239000008139 complexing agent Substances 0.000 claims abstract description 5
- 150000002978 peroxides Chemical class 0.000 claims description 25
- -1 ketone peroxides Chemical class 0.000 claims description 23
- 229920000642 polymer Polymers 0.000 claims description 20
- 239000000203 mixture Substances 0.000 claims description 14
- 150000001875 compounds Chemical class 0.000 claims description 11
- 125000004432 carbon atom Chemical group C* 0.000 claims description 10
- 239000002904 solvent Substances 0.000 claims description 10
- 125000000217 alkyl group Chemical group 0.000 claims description 7
- 229910052739 hydrogen Inorganic materials 0.000 claims description 7
- 239000001257 hydrogen Substances 0.000 claims description 6
- 229920001567 vinyl ester resin Polymers 0.000 claims description 6
- 150000002432 hydroperoxides Chemical class 0.000 claims description 5
- 238000002156 mixing Methods 0.000 claims description 5
- 150000002431 hydrogen Chemical group 0.000 claims description 4
- 125000003545 alkoxy group Chemical group 0.000 claims description 3
- 229910052760 oxygen Inorganic materials 0.000 claims description 3
- 229920006337 unsaturated polyester resin Polymers 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 2
- 150000004978 peroxycarbonates Chemical class 0.000 claims description 2
- 239000004925 Acrylic resin Substances 0.000 claims 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 22
- 239000000178 monomer Substances 0.000 description 10
- 239000003446 ligand Substances 0.000 description 9
- 229920006305 unsaturated polyester Polymers 0.000 description 9
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 6
- 150000007942 carboxylates Chemical class 0.000 description 6
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 6
- 230000008569 process Effects 0.000 description 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 4
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 4
- 229920000180 alkyd Polymers 0.000 description 4
- 150000001412 amines Chemical class 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 239000000835 fiber Substances 0.000 description 4
- 239000000945 filler Substances 0.000 description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
- 150000003254 radicals Chemical class 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- OBETXYAYXDNJHR-UHFFFAOYSA-N 2-Ethylhexanoic acid Chemical compound CCCCC(CC)C(O)=O OBETXYAYXDNJHR-UHFFFAOYSA-N 0.000 description 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 229910052783 alkali metal Inorganic materials 0.000 description 3
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 3
- 239000002585 base Substances 0.000 description 3
- SHZIWNPUGXLXDT-UHFFFAOYSA-N caproic acid ethyl ester Natural products CCCCCC(=O)OCC SHZIWNPUGXLXDT-UHFFFAOYSA-N 0.000 description 3
- 229910017052 cobalt Inorganic materials 0.000 description 3
- 239000010941 cobalt Substances 0.000 description 3
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical group [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 3
- 229920000647 polyepoxide Polymers 0.000 description 3
- DQWPFSLDHJDLRL-UHFFFAOYSA-N triethyl phosphate Chemical compound CCOP(=O)(OCC)OCC DQWPFSLDHJDLRL-UHFFFAOYSA-N 0.000 description 3
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 2
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
- HECLRDQVFMWTQS-RGOKHQFPSA-N 1755-01-7 Chemical compound C1[C@H]2[C@@H]3CC=C[C@@H]3[C@@H]1C=C2 HECLRDQVFMWTQS-RGOKHQFPSA-N 0.000 description 2
- BJELTSYBAHKXRW-UHFFFAOYSA-N 2,4,6-triallyloxy-1,3,5-triazine Chemical compound C=CCOC1=NC(OCC=C)=NC(OCC=C)=N1 BJELTSYBAHKXRW-UHFFFAOYSA-N 0.000 description 2
- WFUGQJXVXHBTEM-UHFFFAOYSA-N 2-hydroperoxy-2-(2-hydroperoxybutan-2-ylperoxy)butane Chemical compound CCC(C)(OO)OOC(C)(CC)OO WFUGQJXVXHBTEM-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 2
- QSJXEFYPDANLFS-UHFFFAOYSA-N Diacetyl Chemical compound CC(=O)C(C)=O QSJXEFYPDANLFS-UHFFFAOYSA-N 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
- 238000011993 High Performance Size Exclusion Chromatography Methods 0.000 description 2
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 2
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 description 2
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 2
- 239000004793 Polystyrene Substances 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 2
- 150000001340 alkali metals Chemical class 0.000 description 2
- 150000001342 alkaline earth metals Chemical class 0.000 description 2
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 2
- 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 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- 150000003983 crown ethers Chemical class 0.000 description 2
- GHVNFZFCNZKVNT-UHFFFAOYSA-N decanoic acid Chemical compound CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 description 2
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 239000003822 epoxy resin Substances 0.000 description 2
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 2
- 230000032050 esterification Effects 0.000 description 2
- 238000005886 esterification reaction Methods 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- LEQAOMBKQFMDFZ-UHFFFAOYSA-N glyoxal Chemical compound O=CC=O LEQAOMBKQFMDFZ-UHFFFAOYSA-N 0.000 description 2
- 125000005843 halogen group Chemical group 0.000 description 2
- MNWFXJYAOYHMED-UHFFFAOYSA-N heptanoic acid Chemical compound CCCCCCC(O)=O MNWFXJYAOYHMED-UHFFFAOYSA-N 0.000 description 2
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 150000002466 imines Chemical class 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- 230000003993 interaction Effects 0.000 description 2
- 239000002555 ionophore Substances 0.000 description 2
- 230000000236 ionophoric effect Effects 0.000 description 2
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
- 150000002736 metal compounds Chemical class 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 2
- 150000002894 organic compounds Chemical class 0.000 description 2
- 239000007800 oxidant agent Substances 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 229920000768 polyamine Polymers 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 229920002223 polystyrene Polymers 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 2
- 239000011342 resin composition Substances 0.000 description 2
- 150000003335 secondary amines Chemical class 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 2
- 230000001988 toxicity Effects 0.000 description 2
- 231100000419 toxicity Toxicity 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
- 229910052723 transition metal Inorganic materials 0.000 description 2
- OBETXYAYXDNJHR-SSDOTTSWSA-M (2r)-2-ethylhexanoate Chemical compound CCCC[C@@H](CC)C([O-])=O OBETXYAYXDNJHR-SSDOTTSWSA-M 0.000 description 1
- ZVZXNYFQDXOOOA-UHFFFAOYSA-N 1,2,2,4,7-pentamethyl-1,4,7-triazonane Chemical compound CN1CCN(C)CC(C)(C)N(C)CC1 ZVZXNYFQDXOOOA-UHFFFAOYSA-N 0.000 description 1
- BEQKKZICTDFVMG-UHFFFAOYSA-N 1,2,3,4,6-pentaoxepane-5,7-dione Chemical compound O=C1OOOOC(=O)O1 BEQKKZICTDFVMG-UHFFFAOYSA-N 0.000 description 1
- DIIIISSCIXVANO-UHFFFAOYSA-N 1,2-Dimethylhydrazine Chemical compound CNNC DIIIISSCIXVANO-UHFFFAOYSA-N 0.000 description 1
- VCZQYTJRWNRPHF-UHFFFAOYSA-N 1,2-dioxin Chemical compound O1OC=CC=C1 VCZQYTJRWNRPHF-UHFFFAOYSA-N 0.000 description 1
- UICXTANXZJJIBC-UHFFFAOYSA-N 1-(1-hydroperoxycyclohexyl)peroxycyclohexan-1-ol Chemical compound C1CCCCC1(O)OOC1(OO)CCCCC1 UICXTANXZJJIBC-UHFFFAOYSA-N 0.000 description 1
- XSZYESUNPWGWFQ-UHFFFAOYSA-N 1-(2-hydroperoxypropan-2-yl)-4-methylcyclohexane Chemical compound CC1CCC(C(C)(C)OO)CC1 XSZYESUNPWGWFQ-UHFFFAOYSA-N 0.000 description 1
- HSOOIVBINKDISP-UHFFFAOYSA-N 1-(2-methylprop-2-enoyloxy)butyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC(CCC)OC(=O)C(C)=C HSOOIVBINKDISP-UHFFFAOYSA-N 0.000 description 1
- ZFPGARUNNKGOBB-UHFFFAOYSA-N 1-Ethyl-2-pyrrolidinone Chemical compound CCN1CCCC1=O ZFPGARUNNKGOBB-UHFFFAOYSA-N 0.000 description 1
- ZOZNCAMOIPYYIK-UHFFFAOYSA-N 1-aminoethylideneazanium;acetate Chemical compound CC(N)=N.CC(O)=O ZOZNCAMOIPYYIK-UHFFFAOYSA-N 0.000 description 1
- KCHNMIKAMRQBHD-UHFFFAOYSA-N 1-hydroperoxypentane Chemical compound CCCCCOO KCHNMIKAMRQBHD-UHFFFAOYSA-N 0.000 description 1
- JSWLXPQVSUEOJQ-UHFFFAOYSA-N 1-nonylperoxynonane Chemical compound CCCCCCCCCOOCCCCCCCCC JSWLXPQVSUEOJQ-UHFFFAOYSA-N 0.000 description 1
- BSZXAFXFTLXUFV-UHFFFAOYSA-N 1-phenylethylbenzene Chemical compound C=1C=CC=CC=1C(C)C1=CC=CC=C1 BSZXAFXFTLXUFV-UHFFFAOYSA-N 0.000 description 1
- OMVSWZDEEGIJJI-UHFFFAOYSA-N 2,2,4-Trimethyl-1,3-pentadienol diisobutyrate Chemical compound CC(C)C(=O)OC(C(C)C)C(C)(C)COC(=O)C(C)C OMVSWZDEEGIJJI-UHFFFAOYSA-N 0.000 description 1
- LTMRRSWNXVJMBA-UHFFFAOYSA-L 2,2-diethylpropanedioate Chemical compound CCC(CC)(C([O-])=O)C([O-])=O LTMRRSWNXVJMBA-UHFFFAOYSA-L 0.000 description 1
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 1
- LCZVSXRMYJUNFX-UHFFFAOYSA-N 2-[2-(2-hydroxypropoxy)propoxy]propan-1-ol Chemical compound CC(O)COC(C)COC(C)CO LCZVSXRMYJUNFX-UHFFFAOYSA-N 0.000 description 1
- SBYMUDUGTIKLCR-UHFFFAOYSA-N 2-chloroethenylbenzene Chemical compound ClC=CC1=CC=CC=C1 SBYMUDUGTIKLCR-UHFFFAOYSA-N 0.000 description 1
- YDWAWYVKEHKQBK-UHFFFAOYSA-N 2-ethylbutanimidamide Chemical compound CCC(CC)C(N)=N YDWAWYVKEHKQBK-UHFFFAOYSA-N 0.000 description 1
- MIRQGKQPLPBZQM-UHFFFAOYSA-N 2-hydroperoxy-2,4,4-trimethylpentane Chemical compound CC(C)(C)CC(C)(C)OO MIRQGKQPLPBZQM-UHFFFAOYSA-N 0.000 description 1
- KPGXRSRHYNQIFN-UHFFFAOYSA-N 2-oxoglutaric acid Chemical compound OC(=O)CCC(=O)C(O)=O KPGXRSRHYNQIFN-UHFFFAOYSA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- DXIJHCSGLOHNES-UHFFFAOYSA-N 3,3-dimethylbut-1-enylbenzene Chemical compound CC(C)(C)C=CC1=CC=CC=C1 DXIJHCSGLOHNES-UHFFFAOYSA-N 0.000 description 1
- FRIBMENBGGCKPD-UHFFFAOYSA-N 3-(2,3-dimethoxyphenyl)prop-2-enal Chemical compound COC1=CC=CC(C=CC=O)=C1OC FRIBMENBGGCKPD-UHFFFAOYSA-N 0.000 description 1
- PYSRRFNXTXNWCD-UHFFFAOYSA-N 3-(2-phenylethenyl)furan-2,5-dione Chemical compound O=C1OC(=O)C(C=CC=2C=CC=CC=2)=C1 PYSRRFNXTXNWCD-UHFFFAOYSA-N 0.000 description 1
- KCHQXPGUJBVNTN-UHFFFAOYSA-N 4,4-diphenylbut-3-en-2-one Chemical compound C=1C=CC=CC=1C(=CC(=O)C)C1=CC=CC=C1 KCHQXPGUJBVNTN-UHFFFAOYSA-N 0.000 description 1
- YPIFGDQKSSMYHQ-UHFFFAOYSA-M 7,7-dimethyloctanoate Chemical compound CC(C)(C)CCCCCC([O-])=O YPIFGDQKSSMYHQ-UHFFFAOYSA-M 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- ROFVEXUMMXZLPA-UHFFFAOYSA-N Bipyridyl Chemical compound N1=CC=CC=C1C1=CC=CC=N1 ROFVEXUMMXZLPA-UHFFFAOYSA-N 0.000 description 1
- 240000008564 Boehmeria nivea Species 0.000 description 1
- NBZCMCOJWDAUTK-UHFFFAOYSA-N C(=C)C12C(C=CC=3C4=CC=CC=C4CC13)O2 Chemical compound C(=C)C12C(C=CC=3C4=CC=CC=C4CC13)O2 NBZCMCOJWDAUTK-UHFFFAOYSA-N 0.000 description 1
- MJXUFBUYCLOLBZ-UHFFFAOYSA-N C(C)(=N)N.CC(=O)C Chemical compound C(C)(=N)N.CC(=O)C MJXUFBUYCLOLBZ-UHFFFAOYSA-N 0.000 description 1
- XLVKQJAUSBDRMV-UHFFFAOYSA-N C(CC)C(C(=N)N)CCC Chemical compound C(CC)C(C(=N)N)CCC XLVKQJAUSBDRMV-UHFFFAOYSA-N 0.000 description 1
- 244000025254 Cannabis sativa Species 0.000 description 1
- 235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 description 1
- 235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 description 1
- 229920000049 Carbon (fiber) Polymers 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- 240000000491 Corchorus aestuans Species 0.000 description 1
- 235000011777 Corchorus aestuans Nutrition 0.000 description 1
- 235000010862 Corchorus capsularis Nutrition 0.000 description 1
- MHZGKXUYDGKKIU-UHFFFAOYSA-N Decylamine Chemical compound CCCCCCCCCCN MHZGKXUYDGKKIU-UHFFFAOYSA-N 0.000 description 1
- 239000004641 Diallyl-phthalate Substances 0.000 description 1
- JYFHYPJRHGVZDY-UHFFFAOYSA-N Dibutyl phosphate Chemical compound CCCCOP(O)(=O)OCCCC JYFHYPJRHGVZDY-UHFFFAOYSA-N 0.000 description 1
- YUXIBTJKHLUKBD-UHFFFAOYSA-N Dibutyl succinate Chemical compound CCCCOC(=O)CCC(=O)OCCCC YUXIBTJKHLUKBD-UHFFFAOYSA-N 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 240000000797 Hibiscus cannabinus Species 0.000 description 1
- QAQJMLQRFWZOBN-LAUBAEHRSA-N L-ascorbyl-6-palmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](O)[C@H]1OC(=O)C(O)=C1O QAQJMLQRFWZOBN-LAUBAEHRSA-N 0.000 description 1
- 239000011786 L-ascorbyl-6-palmitate Substances 0.000 description 1
- PEEHTFAAVSWFBL-UHFFFAOYSA-N Maleimide Chemical compound O=C1NC(=O)C=C1 PEEHTFAAVSWFBL-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 description 1
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 229920000604 Polyethylene Glycol 200 Polymers 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
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- LCTONWCANYUPML-UHFFFAOYSA-M Pyruvate Chemical compound CC(=O)C([O-])=O LCTONWCANYUPML-UHFFFAOYSA-M 0.000 description 1
- DFPOZTRSOAQFIK-UHFFFAOYSA-N S,S-dimethyl-beta-propiothetin Chemical compound C[S+](C)CCC([O-])=O DFPOZTRSOAQFIK-UHFFFAOYSA-N 0.000 description 1
- 229920000147 Styrene maleic anhydride Polymers 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 229920000561 Twaron Polymers 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- KIEZCQDQEPYXOS-UHFFFAOYSA-N [2,2,4-trimethyl-1-(2-methylpropanoyloxy)pentyl] 2-methylpropanoate Chemical compound CC(C)CC(C)(C)C(OC(=O)C(C)C)OC(=O)C(C)C KIEZCQDQEPYXOS-UHFFFAOYSA-N 0.000 description 1
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 description 1
- 150000004729 acetoacetic acid derivatives Chemical class 0.000 description 1
- 235000019401 acetone peroxide Nutrition 0.000 description 1
- 239000000011 acetone peroxide Substances 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 238000007605 air drying Methods 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 238000004873 anchoring Methods 0.000 description 1
- 239000004760 aramid Substances 0.000 description 1
- 150000004982 aromatic amines Chemical class 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 229920003235 aromatic polyamide Polymers 0.000 description 1
- 229940072107 ascorbate Drugs 0.000 description 1
- 235000010323 ascorbic acid Nutrition 0.000 description 1
- 239000011668 ascorbic acid Substances 0.000 description 1
- 235000010385 ascorbyl palmitate Nutrition 0.000 description 1
- WURBFLDFSFBTLW-UHFFFAOYSA-N benzil Chemical compound C=1C=CC=CC=1C(=O)C(=O)C1=CC=CC=C1 WURBFLDFSFBTLW-UHFFFAOYSA-N 0.000 description 1
- 235000019445 benzyl alcohol Nutrition 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- QUDWYFHPNIMBFC-UHFFFAOYSA-N bis(prop-2-enyl) benzene-1,2-dicarboxylate Chemical compound C=CCOC(=O)C1=CC=CC=C1C(=O)OCC=C QUDWYFHPNIMBFC-UHFFFAOYSA-N 0.000 description 1
- JKJWYKGYGWOAHT-UHFFFAOYSA-N bis(prop-2-enyl) carbonate Chemical compound C=CCOC(=O)OCC=C JKJWYKGYGWOAHT-UHFFFAOYSA-N 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 210000004556 brain Anatomy 0.000 description 1
- OWBTYPJTUOEWEK-UHFFFAOYSA-N butane-2,3-diol Chemical compound CC(O)C(C)O OWBTYPJTUOEWEK-UHFFFAOYSA-N 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- 235000009120 camo Nutrition 0.000 description 1
- 239000004917 carbon fiber Substances 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 238000009750 centrifugal casting Methods 0.000 description 1
- 235000005607 chanvre indien Nutrition 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 150000001868 cobalt Chemical class 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- FOTKYAAJKYLFFN-UHFFFAOYSA-N decane-1,10-diol Chemical compound OCCCCCCCCCCO FOTKYAAJKYLFFN-UHFFFAOYSA-N 0.000 description 1
- OECVZYCWCAIRDK-UHFFFAOYSA-N decane;hydrogen peroxide Chemical compound OO.CCCCCCCCCC OECVZYCWCAIRDK-UHFFFAOYSA-N 0.000 description 1
- 239000003975 dentin desensitizing agent Substances 0.000 description 1
- 239000002274 desiccant Substances 0.000 description 1
- 125000004386 diacrylate group Chemical group 0.000 description 1
- JBSLOWBPDRZSMB-FPLPWBNLSA-N dibutyl (z)-but-2-enedioate Chemical compound CCCCOC(=O)\C=C/C(=O)OCCCC JBSLOWBPDRZSMB-FPLPWBNLSA-N 0.000 description 1
- BVXOPEOQUQWRHQ-UHFFFAOYSA-N dibutyl phosphite Chemical compound CCCCOP([O-])OCCCC BVXOPEOQUQWRHQ-UHFFFAOYSA-N 0.000 description 1
- 229960002097 dibutylsuccinate Drugs 0.000 description 1
- 150000005690 diesters Chemical class 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- UCQFCFPECQILOL-UHFFFAOYSA-N diethyl hydrogen phosphate Chemical compound CCOP(O)(=O)OCC UCQFCFPECQILOL-UHFFFAOYSA-N 0.000 description 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
- GGSUCNLOZRCGPQ-UHFFFAOYSA-N diethylaniline Chemical compound CCN(CC)C1=CC=CC=C1 GGSUCNLOZRCGPQ-UHFFFAOYSA-N 0.000 description 1
- 229940028356 diethylene glycol monobutyl ether Drugs 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- FYZZJDABXBPMOG-UHFFFAOYSA-N ethanol;n-methylmethanamine Chemical compound CCO.CNC FYZZJDABXBPMOG-UHFFFAOYSA-N 0.000 description 1
- 150000004665 fatty acids Chemical group 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 238000009730 filament winding Methods 0.000 description 1
- 238000009408 flooring Methods 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 1
- 229940015043 glyoxal Drugs 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000011487 hemp Substances 0.000 description 1
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- UAORAKLVHWMDLY-UHFFFAOYSA-N hydrazine hydrogen peroxide Chemical compound NN.OO UAORAKLVHWMDLY-UHFFFAOYSA-N 0.000 description 1
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 239000000976 ink Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 1
- 239000000347 magnesium hydroxide Substances 0.000 description 1
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- SYBYTAAJFKOIEJ-UHFFFAOYSA-N methyl iso-propyl ketone Natural products CC(C)C(C)=O SYBYTAAJFKOIEJ-UHFFFAOYSA-N 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 150000002762 monocarboxylic acid derivatives Chemical class 0.000 description 1
- GYVGXEWAOAAJEU-UHFFFAOYSA-N n,n,4-trimethylaniline Chemical compound CN(C)C1=CC=C(C)C=C1 GYVGXEWAOAAJEU-UHFFFAOYSA-N 0.000 description 1
- YKYONYBAUNKHLG-UHFFFAOYSA-N n-Propyl acetate Natural products CCCOC(C)=O YKYONYBAUNKHLG-UHFFFAOYSA-N 0.000 description 1
- 125000005609 naphthenate group Chemical group 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- WWZKQHOCKIZLMA-UHFFFAOYSA-M octanoate Chemical compound CCCCCCCC([O-])=O WWZKQHOCKIZLMA-UHFFFAOYSA-M 0.000 description 1
- 125000005474 octanoate group Chemical group 0.000 description 1
- 230000009965 odorless effect Effects 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- MMCOUVMKNAHQOY-UHFFFAOYSA-L oxido carbonate Chemical compound [O-]OC([O-])=O MMCOUVMKNAHQOY-UHFFFAOYSA-L 0.000 description 1
- JCGNDDUYTRNOFT-UHFFFAOYSA-N oxolane-2,4-dione Chemical compound O=C1COC(=O)C1 JCGNDDUYTRNOFT-UHFFFAOYSA-N 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 229930015698 phenylpropene Natural products 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 150000003003 phosphines Chemical class 0.000 description 1
- UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 description 1
- 150000003009 phosphonic acids Chemical class 0.000 description 1
- 150000003018 phosphorus compounds Chemical class 0.000 description 1
- 229910000073 phosphorus hydride Inorganic materials 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000193 polymethacrylate Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 150000004032 porphyrins Chemical class 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- 229940090181 propyl acetate Drugs 0.000 description 1
- ROSDSFDQCJNGOL-UHFFFAOYSA-N protonated dimethyl amine Natural products CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 229920005604 random copolymer Polymers 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 235000015096 spirit Nutrition 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 150000003440 styrenes Chemical class 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
- ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- UWHCKJMYHZGTIT-UHFFFAOYSA-N tetraethylene glycol Chemical compound OCCOCCOCCOCCO UWHCKJMYHZGTIT-UHFFFAOYSA-N 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 238000001721 transfer moulding Methods 0.000 description 1
- 229910001428 transition metal ion Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- STCOOQWBFONSKY-UHFFFAOYSA-N tributyl phosphate Chemical compound CCCCOP(=O)(OCCCC)OCCCC STCOOQWBFONSKY-UHFFFAOYSA-N 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- 150000004684 trihydrates Chemical class 0.000 description 1
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 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
Classifications
-
- 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
- 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
- C08J3/02—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques
-
- 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
- C08J3/02—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques
- C08J3/09—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques in organic liquids
-
- 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
- C08J3/02—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques
- C08J3/09—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques in organic liquids
- C08J3/091—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques in organic liquids characterised by the chemical constitution of the organic liquid
- C08J3/095—Oxygen containing compounds
-
- 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
-
- 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
- C08K5/0091—Complexes with metal-heteroatom-bonds
-
- 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
- C08K5/06—Ethers; Acetals; Ketals; Ortho-esters
-
- 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
- C08K5/14—Peroxides
-
- 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
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/52—Phosphorus bound to oxygen only
- C08K5/521—Esters of phosphoric acids, e.g. of H3PO4
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L33/00—Compositions of homopolymers or copolymers 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 of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- C08L33/04—Homopolymers or copolymers of esters
- C08L33/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, which oxygen atoms are present only as part of the carboxyl radical
- C08L33/08—Homopolymers or copolymers of acrylic acid esters
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L33/00—Compositions of homopolymers or copolymers 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 of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- C08L33/04—Homopolymers or copolymers of esters
- C08L33/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, which oxygen atoms are present only as part of the carboxyl radical
- C08L33/10—Homopolymers or copolymers of methacrylic acid esters
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L35/00—Compositions of 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 a carboxyl radical, and containing at least one other carboxyl radical in the molecule, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- C08L35/02—Homopolymers or copolymers of esters
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
- C08L67/06—Unsaturated polyesters
-
- 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
- C08J2331/00—Characterised by the use of 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 an acyloxy radical of a saturated carboxylic acid, or carbonic acid, or of a haloformic acid
- C08J2331/02—Characterised by the use of omopolymers or copolymers of esters of monocarboxylic acids
- C08J2331/04—Homopolymers or copolymers of vinyl acetate
-
- 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
- C08J2333/00—Characterised by the use of homopolymers or copolymers 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 of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers
- C08J2333/04—Characterised by the use of homopolymers or copolymers 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 of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers esters
- C08J2333/06—Characterised by the use of homopolymers or copolymers 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 of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers esters of esters containing only carbon, hydrogen, and oxygen, the oxygen atom being present only as part of the carboxyl radical
- C08J2333/10—Homopolymers or copolymers of methacrylic acid esters
-
- 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
- C08J2367/00—Characterised by the use of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Derivatives of such polymers
- C08J2367/06—Unsaturated polyesters
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Dispersion Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Macromonomer-Based Addition Polymer (AREA)
- Polymerization Catalysts (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
Abstract
本發明係關於一種固化自由基可固化樹脂之方法,其係藉由向該樹脂添加有機過氧化物及帶金屬聚合物來進行,該帶金屬聚合物包含與選自由Cu、Mn、Fe及V組成之群的金屬配位且與該金屬及錯合劑一起形成錯合物之官能基。
Description
本發明係關於一種加速用有機過氧化物經氧化還原系統固化自由基可固化樹脂之方法。
習知氧化還原系統包含氧化劑(例如過氧化物)及作為加速劑之可溶性過渡金屬離子。加速劑用於提高氧化劑在低溫下之活性,且因此加速固化。
加速劑系統可添加至欲以不同方式固化之樹脂。一種方法涉及在添加過氧化物之前將個別加速劑成分添加至樹脂。此可在即將添加過氧化物之前進行或在添加過氧化物前幾天或幾週進行。在添加過氧化物前幾天或幾週進行的情況下,吾人提及預加速之樹脂組合物,其包含樹脂及加速劑成分且可儲存直至進一步使用及用過氧化物固化。
另一方法涉及預先製備含有加速劑成分之加速劑溶液,該溶液可儲存直至進一步使用及添加至樹脂。經預加速之樹脂可藉由將加速劑系統之個別成分添加至樹脂或藉由添加呈加速劑溶液形式之此等成分之混合物來製備。
典型加速劑系統包含過渡金屬鹽或錯合物。用於此目的之最常用過渡金屬為鈷。然而,鑒於鈷之毒性,法規要求減少鈷之量。
因此,需要提供無Co之加速劑。揭示此類無Co之加速劑系統之文獻實例為WO 2008/003492、WO 2008/003793及WO 2008/003500。根據此等文獻,用於加速劑系統之金屬為Mn、Cu、Fe及Ti而非Co。
所揭示之加速劑系統以經預加速之樹脂形式存在於不飽和聚酯或乙烯基酯樹脂中。據稱此經預加速之樹脂每公斤樹脂含有小於0.01mmol Co。
此等申請案中所揭示之金屬化合物為金屬羧酸鹽、乙醯乙酸鹽及氯化物。雖然比許多鈷鹽及錯合物害處小,但此等金屬化合物中有許多亦存在毒性及環境問題。因此,需要甚至較少健康及/或環境問題之加速劑系統。
本發明提供此類系統。本發明係關於一種固化自由基可固化樹脂之方法,其向該樹脂添加有機過氧化物及帶金屬聚合物,該帶金屬聚合物包含與選自由Cu、Mn、Fe及V組成之群的金屬配位且與該金屬及錯合劑一起形成錯合物之官能基。
術語「配位」及「錯合物」在本說明書中係關於金屬與有機化合物之間任何形式之相互作用,以離子鍵或金屬配位基相互作用形式。
本發明亦關於一種適用於與過氧化物形成氧化還原對且包含帶金屬聚合物及溶劑之加速劑溶液。
本發明亦關於一種包含用該帶金屬聚合物預加速之樹脂及有機過氧化物的雙組分組合物。
應注意帶Mn聚合物已揭示於WO 2012/000934中。此聚合物在醇酸樹脂基油漆及油墨中用作乾燥劑。然而,此醇酸樹脂固化涉及風乾方法;非類似本發明方法使用過氧化物的自由基方法。
帶金屬聚合物可為任何類型聚合物,包括均聚物、無規共聚物及嵌段共聚物。適合聚合物之實例為聚苯乙烯、苯乙烯-順丁烯二酸酐共聚物、聚丙烯酸酯或聚甲基丙烯酸酯、飽和或不飽和聚酯、聚醯胺及聚醯亞胺。聚酯為最佳的。甚至更佳為不飽和聚酯。
聚合物較佳為極性的。此例如與醇酸樹脂形成對比,後者因其
脂肪酸鏈而極具非極性。
聚合物之重量平均分子量較佳在500g/mol至50,000g/mol,更佳1,000g/mol至20,000g/mol,且最佳5,000g/mol至10,000g/mol範圍內。此分子量使用聚苯乙烯標準物,藉由高效尺寸排外層析法(HP-SEC)來測定。
存在於聚合物上之官能基之實例為胺、羧酸酯、膦酸酯、膦酸、膦、1,3-二酮、具有結構R-C(=O)-CH2-C(=NR)-R之亞胺及諸如雙吡酮(bispidon)配位基(諸如,2,4-二(2-吡啶基)-3-甲基-7-(吡啶-2-基甲基)-3,7-二氮-雙環[3.3.1]壬-9-酮-1,5-二甲酸二甲酯三甲基-1,4,7-三氮雜環壬烷)、冠醚、氮雜-冠醚、苯并-冠醚、卟啉(porphirine)及離子載體之配位基。
最佳為胺、羧酸酯、1,3-二酮及雙吡酮配位基。
此等官能基可例如以描述於A.G.Talma等人,Synthesis 1986,680-683中之方式,在製備聚合物期間藉由共聚合具有所需官能基之單體引入聚合物。配位基官能化單體可藉由首先用可與適合單體(例如,羥基及胺基)反應之基團官能化該配位基,之後使該官能化配位基與單體反應來製備。
亦有可能例如經由加成化學或縮合反應(例如,醯胺化或酯化)將配位基或官能基引入現有聚合物。
金屬可添加至官能化聚合物,或可在製備該官能化聚合物期間已存在。
帶金屬聚合物之金屬含量較佳在以帶金屬聚合物重量計0.01wt%至15wt%,更佳0.1wt%至10wt%,且最佳1wt%至5wt%範圍內。此金屬含量可易於藉由ICP測定。
金屬係選自由Cu、Mn、Fe及V組成之群。較佳金屬為Cu、Fe及V。
金屬由該聚合物中之官能基且由錯合劑兩者錯合。此錯合劑可選自帶羧酸酯化合物、1,3-二酮、鹵素原子、胺、膦酸酯、膦酸、膦、具有結構R-C(=O)-CH2-C(=NR)-R之亞胺及諸如冠醚、氮雜-冠醚、苯并-冠醚、卟啉及離子載體之配位基。
適合帶羧酸酯化合物之實例為2-乙基己酸酯、辛酸酯、壬酸酯、庚酸酯、新癸酸酯、環烷酸酯及如上文所描述之帶羧酸酯聚合物。
1,3-二酮之實例為乙醯基丙酮、苯甲醯基丙酮及二苯甲醯基甲烷,及乙醯乙酸酯諸如二乙基乙醯乙醯胺、二甲基乙醯乙醯胺、二丙基乙醯乙醯胺、二丁基乙醯乙醯胺、乙醯乙酸甲酯、乙醯乙酸乙酯、乙醯乙酸丙酯及乙醯乙酸丁酯。
較佳鹵素原子為Cl。
帶金屬聚合物可用於加速不飽和樹脂之自由基固化。帶金屬聚合物可按原樣或以除帶金屬聚合物外含有溶劑及視情況存在之其他化合物的所謂加速劑溶液形式添加至樹脂中。
帶金屬聚合物可在即將添加過氧化物之前或在添加過氧化物之前幾天或幾週添加至樹脂(按原樣或以加速劑溶液形式)。在在添加過氧化物之前幾天或幾週添加的情況下,吾人提及經預加速之樹脂。
適合溶劑之實例為磷化合物及羥基官能性溶劑。較佳地,加速劑溶液含有至少一種選自以下之溶劑:具有式P(R)3、P(R)3=O及HO-(-CH2-C(R1)2-(CH2)m-O-)n-R2之化合物,其中各R獨立地選自氫、具有1至10個碳原子之烷基及具有1至10個碳原子之烷氧基,各R1獨立地選自由氫、具有1至10個碳原子之烷基及具有1至10個碳原子之羥基烷基組成之群,n=1至10,m=0或1,且R2為氫或具有1至10個碳原子之烷基。
較佳地,在具有式P(R)3及P(R)3=O之亞磷酸化合物中,至少兩個R基團係選自烷基或烷氧基。適合含亞磷酸化合物之特定實例為磷酸
二乙酯、磷酸二丁酯、磷酸三丁酯、磷酸三乙酯(TEP)、亞磷酸二丁酯及磷酸三乙酯。
在式HO-(-CH2-C(R1)2-(CH2)m-O-)n-R2中,各R1較佳獨立選自H、CH3及CH2OH。此類溶劑之實例為二醇,如二乙二醇單丁醚、乙二醇、二乙二醇、二丙二醇及聚乙二醇、甘油及異戊四醇。
另外,加速劑溶液可包含額外有機化合物,諸如脂族烴溶劑(例如白色石油腦、石蠟或無味礦油精(OMS));芳族烴溶劑(例如萘或萘混合物);醛;酮(例如1,2-二酮,如丁二酮或乙二醛);醚;酯(例如順丁烯二酸二丁酯、丁二酸二丁酯、乙酸乙酯、乙酸丁酯、酮戊二酸之單酯及二酯、丙酮酸酯、抗壞血酸酯(諸如抗壞血酸棕櫚酸酯、丙二酸二乙酯或丁二酸酯);醇類(例如異丁醇、戊醇、苯甲醇或脂肪醇);磷酸鹽;醯胺;羧酸;1,2-二肟;N-甲基吡咯啶酮;N-乙基吡咯啶酮;二甲基甲醯胺(DMF);二甲亞碸(DMSO);及2,2,4-三甲基戊二醇二異丁酸酯(TXIB);加速劑溶液及經預加速之樹脂可視情況含有一或多種促進劑、鹼、水、抑制劑、添加劑及/或填充劑。
適合促進劑為銨、鹼金屬或鹼土金屬之羧酸鹽。適合銨、鹼金屬及鹼土金屬之適合金屬羰酸鹽之實例為2-乙基己酸鹽(亦即辛酸鹽)、壬酸鹽、庚酸鹽、新庚酸鹽及萘酸鹽。較佳鹼金屬為K。鹽可按原樣添加至加速劑溶液或樹脂中,或其可當場形成。舉例而言,鹼金屬2-乙基己酸鹽可在將鹼金屬氫氧化物及2-乙基己酸添加至溶液之後在加速劑溶液中當場製備。
若一或多種促進劑存在於加速劑溶液中,則其量較佳為至少0.01wt%,更佳至少0.1wt%,甚至更佳至少1wt%,更佳至少10wt%,且最佳至少20wt%;較佳不超過90wt%,更佳不超過80wt%,且最佳不超過70wt%,均以加速劑溶液之總重量計。
待存在於加速劑溶液及經預加速之樹脂中的適合含氮鹼為一級胺、二級胺及三級胺,諸如三乙胺、二甲基苯胺、二乙基苯胺或N,N-二甲基-對-甲苯胺(DMPT);多元胺,諸如1,2-(二甲基胺)乙烷;二級胺,諸如二乙胺;乙氧基化胺,諸如三乙醇胺、二甲胺基乙醇、二乙醇胺或單乙醇胺;及芳族胺,諸如吡啶或聯吡啶。含氮鹼較佳以5wt%至50wt%之量存在於加速劑溶液中。其較佳以0.5g/kg樹脂至10g/kg樹脂之量存在於經預加速之樹脂中。
加速劑溶液可視情況包含水。若存在,則溶液之水含量較佳為至少0.01wt%且更佳至少0.1wt%。水含量較佳不超過50wt%,更佳不超過40wt%,更佳不超過20wt%,甚至更佳不超過10wt%,且最佳不超過5wt%,均以加速劑溶液之總重量計。
加速劑溶液可藉由簡單地混合各成分,視情況伴以中間加熱及/或混合步驟來製備。
經預加速之樹脂可以不同方式製備:藉由混合個別成分與樹脂,或藉由混合包括視情況選用之單體的樹脂與根據本發明之加速劑溶液。混合包括視情況選用之單體的樹脂與根據本發明之加速劑溶液的方法較佳。
待根據本發明方法固化之適合樹脂包括醇酸樹脂、不飽和聚酯(UP)樹脂、乙烯基酯樹脂、(甲基)丙烯酸酯樹脂、聚胺基甲酸酯、環氧樹脂及其混合物。較佳樹脂為(甲基)丙烯酸酯樹脂、UP樹脂及乙烯基酯樹脂。
在本申請案之上下文中,術語「不飽和聚酯樹脂」及「UP樹脂」係指不飽和聚酯樹脂與烯系不飽和單體化合物之組合。術語乙烯基酯樹脂係指藉由環氧樹脂與不飽和單羧酸酯化產生,且溶解於烯系不飽和單體化合物(例如苯乙烯)中之樹脂。如上文所定義之UP樹脂及乙烯基酯樹脂為慣例且市場有售。
藉由本發明之方法固化之適合UP樹脂為所謂鄰位型樹脂、間位型樹脂、間位-npg型樹脂及二環戊二烯(DCPD)樹脂。此類樹脂之實例為順丁烯二酸、反丁烯二酸、烯丙基、乙烯系及環氧樹脂型樹脂、雙酚A樹脂、對苯二甲酸樹脂及雜化樹脂。
不含額外烯系不飽和單體化合物(如苯乙烯)之丙烯酸酯及甲基丙烯酸脂樹脂在本申請案中稱為(甲基)丙烯酸酯樹脂。
烯系不飽和單體化合物之實例包括苯乙烯及苯乙烯衍生物,如α-甲苯苯乙烯、乙烯基甲苯、茚、二乙烯基苯、乙烯基吡咯啶酮、乙烯基矽氧烷、乙烯基己內醯胺、芪,及亦鄰苯二甲酸二烯丙酯、二苯亞甲基丙酮、烯丙基苯、甲基丙烯酸甲酯、丙烯酸甲酯、(甲基)丙烯酸、二丙烯酸酯、二甲基丙烯酸酯、丙烯醯胺;乙酸乙烯酯、三聚氰酸三烯丙酯、異三聚氰酸三烯丙酯、用於光學應用之烯丙基化合物(諸如(二)乙二醇二烯丙基碳酸酯)、氯苯乙烯、第三丁基苯乙烯、丙烯酸第三丁酯、丁二醇二甲基丙烯酸酯及其混合物。(甲基)丙烯酸酯反應性稀釋劑之適合實例為PEG200二(甲基)丙烯酸酯、1,4-丁二醇二(甲基)丙烯酸酯、1,3-丁二醇二(甲基)丙烯酸酯、2,3-丁二醇二(甲基)丙烯酸酯、1,6-己二醇二(甲基)丙烯酸酯及其異構體;二乙二醇二(甲基)丙烯酸酯、三乙二醇二(甲基)丙烯酸酯、甘油二(甲基)丙烯酸酯、三羥甲基丙烷二(甲基)丙烯酸酯、新戊二醇二(甲基)丙烯酸酯、二丙二醇二(甲基)丙烯酸酯、三丙二醇二(甲基)丙烯酸酯、PPG250二(甲基)丙烯酸酯、三環癸烷二羥甲基二(甲基)丙烯酸酯、1,10-癸二醇二(甲基)丙烯酸酯、四乙二醇二(甲基)丙烯酸酯、三羥甲基丙烷三(甲基)丙烯酸酯、(甲基)丙烯酸縮水甘油酯、(雙)順丁烯二醯亞胺、(雙)甲順丁烯二醯胺、(雙)衣康醯亞胺及其混合物。
烯系不飽和單體在經預加速之樹脂中之量較佳為以樹脂重量計之至少0.1wt%,更佳至少1wt%,且最佳至少5wt%。烯系不飽和單
體之量較佳為不超過50wt%,更佳不超過40wt%,且最佳不超過35wt%。
若加速劑溶液用於固化樹脂或用於製備經預加速之樹脂,則加速劑溶液一般以樹脂之重量計至少0.01wt%,較佳至少0.1wt%,且較佳不超過5wt%,更佳不超過3wt%加速劑溶液之量使用。
適用於固化樹脂且適用於存在於雙組分組合物之第二組分中的過氧化物包括無機過氧化物及有機過氧化物,諸如習知使用之酮過氧化物、過氧基酯、二芳基過氧化物、二烷基過氧化物及過氧基二碳酸酯;及亦過氧基碳酸酯、過氧基縮酮、氫過氧化物、二醯基過氧化物及過氧化氫。較佳過氧化物為有機氫過氧化物、酮過氧化物、過氧基酯及過氧基碳酸酯。甚至更佳為氫過氧化物及酮過氧化物。較佳氫過氧化物包括異丙苯過氧化氫、1,1,3,3-四甲基丁基氫過氧化物、第三丁基氫過氧化物、異丙基茴香基氫過氧化物、第三戊基氫過氧化物、2,5-二甲基己基-2,5-二氫過氧化物、蒎烷氫過氧化物、對-薄荷烷-氫過氧化物、萜類-氫過氧化物及蒎烯氫過氧化物。較佳酮過氧化物包括甲基乙基酮過氧化物、甲基異丙基酮過氧化物、甲基異丁基酮過氧化物、環己酮過氧化物及乙醯丙酮過氧化物。
當然,亦可使用兩種或兩種以上過氧化物之混合物;例如氫過氧化物或酮過氧化物與過氧基酯之組合。
尤其較佳之過氧化物為甲基乙基酮過氧化物。熟習此項技術者應理解此等過氧化物可與習知添加劑(例如填充劑、顏料及減敏劑)組合。減敏劑之實例為親水性酯及烴溶劑。待用於固化樹脂之過氧化物之量較佳為每100份樹脂至少0.1(phr),更佳至少0.5phr,且最佳至少1phr。過氧化物之量較佳不超過8phr,更佳不超過5phr,最佳不超過2phr。
固化一般藉由將根據本發明之加速劑溶液及起始劑(過氧化物)添
加至樹脂中,或藉由將過氧化物添加至經預加速之樹脂開始。換言之,過氧化物可添加至經預加速之樹脂,添加至樹脂與加速劑溶液之預混物,或在添加加速劑溶液之前添加至樹脂。
混合且分散所得混合物。視引發劑系統、加速劑系統、調適固化速率之化合物及待固化之樹脂組合物而定,固化製程可在-15℃至250℃之任何溫度下進行。較佳地,其在諸如手工塗佈、噴佈、長絲捲繞、樹脂轉移模製、塗佈(例如凝膠塗佈及標準塗佈)、按鈕製造、離心鑄造、波紋薄片或扁平面板、換襯系統、傾倒化合物之廚房水槽等應用中常用之環境溫度下進行。然而,其亦可用於SMC、BMC、拉擠成形技術及其類似技術,上述技術使用高達180℃,更佳高達150℃,最佳高達100℃之溫度。
諸如填充劑、纖維、顏料、抑制劑、輔劑及促進劑之其他視情況選用之添加劑可用於固化製程。
纖維之實例為玻璃纖維、碳纖維、芳族聚醯胺纖維(例如Twaron®)、天然纖維(例如黃麻、洋麻、工業大麻、亞麻(亞麻布)、苧麻等)。
填充劑之實例為石英、沙石、三水合氧化鋁、氫氧化鎂、白堊、氫氧化鈣、黏土及石灰。
固化樹脂可經受固化後處理以進一步使硬度最佳化。此類固化後處理一般在40℃至180℃溫度範圍內進行30分鐘至15小時。
固化樹脂可用於不同應用,包括海事應用、化學錨定、屋面、建築、換襯、管道及貯槽、地板、風車葉片、層壓製品等。
Claims (11)
- 一種固化自由基可固化樹脂之方法,其係藉由向該樹脂添加有機過氧化物及帶金屬聚合物來進行,該帶金屬聚合物包含與選自由Cu、Mn、Fe及V組成之群的金屬配位且與該金屬及錯合劑一起形成錯合物之官能基。
- 如請求項1之方法,其中該樹脂為不飽和聚酯樹脂、乙烯基酯樹脂或(甲基)丙烯酸酯樹脂。
- 如請求項1之方法,其中該金屬係選自由Cu、Fe及V組成之群。
- 一種適用於與過氧化物形成氧化還原對之加速劑溶液,其包含:至少一種選自具有式P(R)3、P(R)3=O及HO-(-CH2-C(R1)2-(CH2)m-O-)n-R2之化合物之溶劑,其中各R獨立選自氫、具有1至10個碳原子之烷基及具有1至10個碳原子之烷氧基,各R1獨立選自由氫、具有1至10個碳原子之烷基及具有1至10個碳原子之羥基烷基組成之群,n=1至10,m=0或1,且R2為氫或具有1至10個碳原子之烷基,及帶金屬聚合物,該帶金屬聚合物包含與選自由Cu、Mn、Fe及V組成之群的金屬配位且與該金屬及錯合劑一起形成錯合物之官能基。
- 如請求項4之加速劑溶液,其中該帶金屬聚合物之金屬含量較佳在0.01wt%至15wt%範圍內。
- 如請求項4或5之加速劑溶液,其中該金屬係選自由Cu、Fe及V組成之群。
- 一種雙組分組合物,其包含第一組分及第二組分,該第一組分包含自由基可固化樹脂及帶金屬聚合物,該帶金屬聚合物包含 與選自由Cu、Mn、Fe及V組成之群的金屬配位且與該金屬及錯合劑一起形成錯合物之官能基;該第二組分包含有機過氧化物。
- 如請求項7之雙組分組合物,其中該過氧化物係選自由有機氫過氧化物、酮過氧化物、過氧基碳酸酯及過氧基酯組成之群。
- 如請求項7或8之雙組分組合物,其中該金屬係選自由Cu、Fe及V組成之群。
- 如請求項1至3中任一項之方法,其中以如請求項4至6中任一項之加速劑溶液形式將該帶金屬聚合物添加至該樹脂中。
- 如請求項1至3中任一項之方法,其包含提供如請求項7至9中任一項之雙組分組合物及混合該第一組分與該第二組分之步驟。
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP13196803 | 2013-12-12 | ||
| ??13196803.4 | 2013-12-12 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| TW201533076A TW201533076A (zh) | 2015-09-01 |
| TWI628197B true TWI628197B (zh) | 2018-07-01 |
Family
ID=49726653
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TW103143527A TWI628197B (zh) | 2013-12-12 | 2014-12-12 | 固化自由基可固化樹脂之方法 |
Country Status (18)
| Country | Link |
|---|---|
| US (1) | US9751994B2 (zh) |
| EP (1) | EP3080193B1 (zh) |
| JP (1) | JP6284642B2 (zh) |
| KR (1) | KR20160098237A (zh) |
| CN (1) | CN105764958B (zh) |
| AR (1) | AR098752A1 (zh) |
| AU (1) | AU2014363690B2 (zh) |
| CA (1) | CA2931759A1 (zh) |
| ES (1) | ES2667693T3 (zh) |
| IL (1) | IL245629A0 (zh) |
| MX (1) | MX2016007293A (zh) |
| MY (1) | MY183065A (zh) |
| PH (1) | PH12016500936A1 (zh) |
| PL (1) | PL3080193T3 (zh) |
| RU (1) | RU2674416C1 (zh) |
| SA (1) | SA516371265B1 (zh) |
| TW (1) | TWI628197B (zh) |
| WO (1) | WO2015086546A1 (zh) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2019238555A1 (en) * | 2018-06-12 | 2019-12-19 | Nouryon Chemicals International B.V. | Process for the production of composite articles |
| CN112724383B (zh) * | 2020-12-29 | 2022-03-18 | 江苏恒力化纤股份有限公司 | 一种高阻隔水蒸汽聚酯薄膜及其制备方法 |
| CN112745493B (zh) * | 2020-12-29 | 2022-08-19 | 江苏恒力化纤股份有限公司 | 一种耐热性聚酯树脂及其制备方法 |
| WO2024126770A1 (en) | 2022-12-16 | 2024-06-20 | Borchers Gmbh | Vanadium complexes with nitrogen and oxygen donor atoms |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101484516A (zh) * | 2006-07-06 | 2009-07-15 | 帝斯曼知识产权资产管理有限公司 | 不饱和聚酯树脂或乙烯基酯树脂组合物 |
| CN102037026A (zh) * | 2008-05-23 | 2011-04-27 | 株式会社三键 | 一液固化型组合物 |
| WO2012000934A1 (en) * | 2010-06-29 | 2012-01-05 | Umicore | Manganese based catalytic dryer for polymer coatings |
| TW201213362A (en) * | 2010-06-16 | 2012-04-01 | Akzo Nobel Chemicals Int Bv | Accelerator solution and process for curing curable resins |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3476532A (en) | 1964-11-25 | 1969-11-04 | Allied Chem | Metal-containing complexes of oxidized polyethylene |
| US3282909A (en) * | 1965-05-18 | 1966-11-01 | Exxon Research Engineering Co | Metallo-organic polymers, their preparation and utility |
| EP0470139B1 (en) * | 1989-04-26 | 1994-01-05 | Akzo Nobel N.V. | Thiolic compound polymerization cocatalysts |
| US5212210A (en) * | 1992-03-18 | 1993-05-18 | Minnesota Mining And Manufacturing Company | Energy curable compositions having improved cure speeds |
| US5419954A (en) * | 1993-02-04 | 1995-05-30 | The Alpha Corporation | Composition including a catalytic metal-polymer complex and a method of manufacturing a laminate preform or a laminate which is catalytically effective for subsequent electroless metallization thereof |
| US6063637A (en) | 1995-12-13 | 2000-05-16 | California Institute Of Technology | Sensors for sugars and other metal binding analytes |
| DK1899386T3 (da) * | 2005-05-31 | 2011-07-11 | Akzo Nobel Nv | Lagerstabil acceleratoropløsning |
| ES1063481Y (es) | 2006-07-03 | 2007-03-01 | Saez Rosanna Pastor | Protector para pies |
| DE602007012103D1 (de) | 2006-07-06 | 2011-03-03 | Dsm Ip Assets Bv | Ungesättigtes polyesterharz enthaltende zusammensetzungen |
| CN101484478A (zh) | 2006-07-06 | 2009-07-15 | 帝斯曼知识产权资产管理有限公司 | 不饱和聚酯树脂或乙烯基酯树脂组合物 |
| MX2009010657A (es) * | 2007-04-02 | 2009-12-16 | Akzo Nobel Nv | Solucion aceleradora. |
| EP2014729A1 (en) | 2007-07-09 | 2009-01-14 | Sicpa Holding S.A. | Vanadium-drier intaglio ink |
| WO2011057673A1 (en) * | 2009-11-13 | 2011-05-19 | Felicitas Grauer | Animal tracking and surveillance system |
-
2014
- 2014-12-09 WO PCT/EP2014/076949 patent/WO2015086546A1/en not_active Ceased
- 2014-12-09 PL PL14809027T patent/PL3080193T3/pl unknown
- 2014-12-09 EP EP14809027.7A patent/EP3080193B1/en not_active Not-in-force
- 2014-12-09 KR KR1020167015524A patent/KR20160098237A/ko not_active Withdrawn
- 2014-12-09 CN CN201480064268.XA patent/CN105764958B/zh not_active Expired - Fee Related
- 2014-12-09 AU AU2014363690A patent/AU2014363690B2/en not_active Ceased
- 2014-12-09 JP JP2016536237A patent/JP6284642B2/ja not_active Expired - Fee Related
- 2014-12-09 CA CA2931759A patent/CA2931759A1/en not_active Abandoned
- 2014-12-09 MY MYPI2016702048A patent/MY183065A/en unknown
- 2014-12-09 US US15/100,511 patent/US9751994B2/en not_active Expired - Fee Related
- 2014-12-09 MX MX2016007293A patent/MX2016007293A/es unknown
- 2014-12-09 ES ES14809027.7T patent/ES2667693T3/es active Active
- 2014-12-09 RU RU2016126611A patent/RU2674416C1/ru not_active IP Right Cessation
- 2014-12-12 AR ARP140104654A patent/AR098752A1/es unknown
- 2014-12-12 TW TW103143527A patent/TWI628197B/zh not_active IP Right Cessation
-
2016
- 2016-05-11 IL IL245629A patent/IL245629A0/en unknown
- 2016-05-20 PH PH12016500936A patent/PH12016500936A1/en unknown
- 2016-06-05 SA SA516371265A patent/SA516371265B1/ar unknown
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101484516A (zh) * | 2006-07-06 | 2009-07-15 | 帝斯曼知识产权资产管理有限公司 | 不饱和聚酯树脂或乙烯基酯树脂组合物 |
| CN102037026A (zh) * | 2008-05-23 | 2011-04-27 | 株式会社三键 | 一液固化型组合物 |
| TW201213362A (en) * | 2010-06-16 | 2012-04-01 | Akzo Nobel Chemicals Int Bv | Accelerator solution and process for curing curable resins |
| WO2012000934A1 (en) * | 2010-06-29 | 2012-01-05 | Umicore | Manganese based catalytic dryer for polymer coatings |
Also Published As
| Publication number | Publication date |
|---|---|
| JP6284642B2 (ja) | 2018-02-28 |
| CA2931759A1 (en) | 2015-06-18 |
| AU2014363690A1 (en) | 2016-06-02 |
| CN105764958A (zh) | 2016-07-13 |
| IL245629A0 (en) | 2016-06-30 |
| AR098752A1 (es) | 2016-06-08 |
| KR20160098237A (ko) | 2016-08-18 |
| US20160297936A1 (en) | 2016-10-13 |
| WO2015086546A1 (en) | 2015-06-18 |
| CN105764958B (zh) | 2017-12-08 |
| PL3080193T3 (pl) | 2018-07-31 |
| US9751994B2 (en) | 2017-09-05 |
| JP2016540081A (ja) | 2016-12-22 |
| MX2016007293A (es) | 2016-08-04 |
| EP3080193B1 (en) | 2018-02-14 |
| PH12016500936A1 (en) | 2016-06-27 |
| AU2014363690B2 (en) | 2017-11-30 |
| ES2667693T3 (es) | 2018-05-14 |
| RU2674416C1 (ru) | 2018-12-07 |
| EP3080193A1 (en) | 2016-10-19 |
| TW201533076A (zh) | 2015-09-01 |
| MY183065A (en) | 2021-02-10 |
| SA516371265B1 (ar) | 2017-12-26 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| TWI548658B (zh) | 用於固化樹脂之加速劑 | |
| TWI555779B (zh) | 加速劑溶液之製備方法 | |
| TWI551634B (zh) | 用於固化樹脂之加速劑 | |
| TWI575018B (zh) | 雙重固化系統 | |
| KR101967724B1 (ko) | 수지 경화용 철계 가속화제 | |
| TWI628197B (zh) | 固化自由基可固化樹脂之方法 | |
| TWI633134B (zh) | 用於固化含(甲基)丙烯酸酯之不飽和聚酯(up)或乙烯酯(ve)樹脂的方法 | |
| TWI613239B (zh) | 固化熱固性樹脂之方法 | |
| TWI591105B (zh) | 固化熱固性樹脂之方法 | |
| TW201627395A (zh) | 固化樹脂系統之方法 | |
| TWI575005B (zh) | 用於固化樹脂之以鐵為基之加速劑 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MM4A | Annulment or lapse of patent due to non-payment of fees |