FI59806C - Foerfarande foer framstaellning av polyesterhartslack - Google Patents

Foerfarande foer framstaellning av polyesterhartslack Download PDF

Info

Publication number: FI59806C
Authority: FI; Finland
Prior art keywords: polyester resin; weight; polycondensate; polyesterhartslack; varnish
Prior art date: 1975-04-10

Application number

FI760947A

Other languages

English (en)

Finnish (fi)

Other versions

FI59806B (fi

FI760947A7 (de

Inventor

Gilbert Chretien

Gerard Ditacroute

Jacques Meyer

Original Assignee

Rhone Poulenc Ind

Priority date (The priority date 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 date listed.)

1975-04-10

Filing date

1976-04-07

Publication date

1981-10-12

1976-04-07 Application filed by Rhone Poulenc Ind filed Critical Rhone Poulenc Ind

1976-10-11 Publication of FI760947A7 publication Critical patent/FI760947A7/fi

1981-06-30 Publication of FI59806B publication Critical patent/FI59806B/fi

1981-10-12 Application granted granted Critical

1981-10-12 Publication of FI59806C publication Critical patent/FI59806C/fi

Links

229920001225 polyester resin Polymers 0.000 description 20
239000004645 polyester resin Substances 0.000 description 20
239000002966 varnish Substances 0.000 description 11
CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 10
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 9
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 9
239000000395 magnesium oxide Substances 0.000 description 9
QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 8
150000008064 anhydrides Chemical class 0.000 description 8
238000006243 chemical reaction Methods 0.000 description 8
AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 8
239000002253 acid Substances 0.000 description 7
150000007513 acids Chemical class 0.000 description 7
238000006116 polymerization reaction Methods 0.000 description 7
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
239000003638 chemical reducing agent Substances 0.000 description 6
239000004922 lacquer Substances 0.000 description 6
238000000034 method Methods 0.000 description 6
239000011541 reaction mixture Substances 0.000 description 6
230000009257 reactivity Effects 0.000 description 6
239000003999 initiator Substances 0.000 description 5
238000006068 polycondensation reaction Methods 0.000 description 5
WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 4
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 4
LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 4
JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 4
239000003795 chemical substances by application Substances 0.000 description 4
229910052802 copper Inorganic materials 0.000 description 4
239000010949 copper Substances 0.000 description 4
150000002009 diols Chemical class 0.000 description 4
239000000178 monomer Substances 0.000 description 4
229920005989 resin Polymers 0.000 description 4
239000011347 resin Substances 0.000 description 4
239000000126 substance Substances 0.000 description 4
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 4
229920002554 vinyl polymer Polymers 0.000 description 4
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-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 compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 3
150000001869 cobalt compounds Chemical class 0.000 description 3
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
125000005609 naphthenate group Chemical group 0.000 description 3
238000002360 preparation method Methods 0.000 description 3
229920006395 saturated elastomer Polymers 0.000 description 3
MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 2
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
241000220317 Rosa Species 0.000 description 2
235000016588 Rosa centifolia Nutrition 0.000 description 2
244000052585 Rosa centifolia Species 0.000 description 2
DYRDKSSFIWVSNM-UHFFFAOYSA-N acetoacetanilide Chemical compound CC(=O)CC(=O)NC1=CC=CC=C1 DYRDKSSFIWVSNM-UHFFFAOYSA-N 0.000 description 2
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 2
239000003086 colorant Substances 0.000 description 2
150000001875 compounds Chemical class 0.000 description 2
238000007334 copolymerization reaction Methods 0.000 description 2
RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 description 2
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
BGTOWKSIORTVQH-UHFFFAOYSA-N cyclopentanone Chemical compound O=C1CCCC1 BGTOWKSIORTVQH-UHFFFAOYSA-N 0.000 description 2
238000000354 decomposition reaction Methods 0.000 description 2
DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 2
238000002845 discoloration Methods 0.000 description 2
FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 2
238000011065 in-situ storage Methods 0.000 description 2
239000003112 inhibitor Substances 0.000 description 2
QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
150000002681 magnesium compounds Chemical class 0.000 description 2
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
239000000203 mixture Substances 0.000 description 2
125000005474 octanoate group Chemical group 0.000 description 2
239000012188 paraffin wax Substances 0.000 description 2
239000003505 polymerization initiator Substances 0.000 description 2
229920005862 polyol Polymers 0.000 description 2
150000003077 polyols Chemical class 0.000 description 2
239000000376 reactant Substances 0.000 description 2
UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 2
POILWHVDKZOXJZ-ARJAWSKDSA-M (z)-4-oxopent-2-en-2-olate Chemical compound C\C([O-])=C\C(C)=O POILWHVDKZOXJZ-ARJAWSKDSA-M 0.000 description 1
150000005207 1,3-dihydroxybenzenes Chemical class 0.000 description 1
AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 description 1
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 1
MMEDJBFVJUFIDD-UHFFFAOYSA-N 2-[2-(carboxymethyl)phenyl]acetic acid Chemical compound OC(=O)CC1=CC=CC=C1CC(O)=O MMEDJBFVJUFIDD-UHFFFAOYSA-N 0.000 description 1
CMPLVXYOKPNUAI-UHFFFAOYSA-N 2-hydroperoxycyclohexan-1-one Chemical compound OOC1CCCCC1=O CMPLVXYOKPNUAI-UHFFFAOYSA-N 0.000 description 1
VYZKQGGPNIFCLD-UHFFFAOYSA-N 3,3-dimethylhexane-2,2-diol Chemical compound CCCC(C)(C)C(C)(O)O VYZKQGGPNIFCLD-UHFFFAOYSA-N 0.000 description 1
OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
BGNXCDMCOKJUMV-UHFFFAOYSA-N Tert-Butylhydroquinone Chemical compound CC(C)(C)C1=CC(O)=CC=C1O BGNXCDMCOKJUMV-UHFFFAOYSA-N 0.000 description 1
UWHCKJMYHZGTIT-UHFFFAOYSA-N Tetraethylene glycol, Natural products OCCOCCOCCOCCO UWHCKJMYHZGTIT-UHFFFAOYSA-N 0.000 description 1
ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
JJHPQGFGFRPCCH-UHFFFAOYSA-N acetic acid;butane Chemical compound CCCC.CC(O)=O JJHPQGFGFRPCCH-UHFFFAOYSA-N 0.000 description 1
150000001252 acrylic acid derivatives Chemical class 0.000 description 1
239000000654 additive Substances 0.000 description 1
239000001361 adipic acid Substances 0.000 description 1
235000011037 adipic acid Nutrition 0.000 description 1
125000000217 alkyl group Chemical group 0.000 description 1
229910000147 aluminium phosphate Inorganic materials 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
IQWSILHONYLIFD-KSBRXOFISA-L benzyl(trimethyl)azanium;(z)-but-2-enedioate Chemical compound [O-]C(=O)\C=C/C([O-])=O.C[N+](C)(C)CC1=CC=CC=C1.C[N+](C)(C)CC1=CC=CC=C1 IQWSILHONYLIFD-KSBRXOFISA-L 0.000 description 1
HCRQJOUBOFIKCF-UHFFFAOYSA-L benzyl(trimethyl)azanium;oxalate Chemical compound [O-]C(=O)C([O-])=O.C[N+](C)(C)CC1=CC=CC=C1.C[N+](C)(C)CC1=CC=CC=C1 HCRQJOUBOFIKCF-UHFFFAOYSA-L 0.000 description 1
BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 1
IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical class C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 1
RFAZFSACZIVZDV-UHFFFAOYSA-N butan-2-one Chemical compound CCC(C)=O.CCC(C)=O RFAZFSACZIVZDV-UHFFFAOYSA-N 0.000 description 1
239000001273 butane Substances 0.000 description 1
IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 1
-1 butene glycols Chemical class 0.000 description 1
239000004202 carbamide Substances 0.000 description 1
125000004432 carbon atom Chemical group C* 0.000 description 1
125000001309 chloro group Chemical class Cl* 0.000 description 1
238000000576 coating method Methods 0.000 description 1
238000009833 condensation Methods 0.000 description 1
230000005494 condensation Effects 0.000 description 1
238000010276 construction Methods 0.000 description 1
238000001816 cooling Methods 0.000 description 1
238000005336 cracking Methods 0.000 description 1
230000001627 detrimental effect Effects 0.000 description 1
229960002380 dibutyl phthalate Drugs 0.000 description 1
SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
230000000694 effects Effects 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
235000019253 formic acid Nutrition 0.000 description 1
238000001879 gelation Methods 0.000 description 1
150000002432 hydroperoxides Chemical class 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
LVHBHZANLOWSRM-UHFFFAOYSA-N itaconic acid Chemical class OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
239000004310 lactic acid Substances 0.000 description 1
235000014655 lactic acid Nutrition 0.000 description 1
239000000314 lubricant Substances 0.000 description 1
229910052749 magnesium Inorganic materials 0.000 description 1
239000011777 magnesium Substances 0.000 description 1
UEGPKNKPLBYCNK-UHFFFAOYSA-L magnesium acetate Chemical compound [Mg+2].CC([O-])=O.CC([O-])=O UEGPKNKPLBYCNK-UHFFFAOYSA-L 0.000 description 1
239000011654 magnesium acetate Substances 0.000 description 1
235000011285 magnesium acetate Nutrition 0.000 description 1
229940069446 magnesium acetate Drugs 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
239000002075 main ingredient Substances 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
150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
GEMHFKXPOCTAIP-UHFFFAOYSA-N n,n-dimethyl-n'-phenylcarbamimidoyl chloride Chemical compound CN(C)C(Cl)=NC1=CC=CC=C1 GEMHFKXPOCTAIP-UHFFFAOYSA-N 0.000 description 1
VHDPPDRSCMVFAV-UHFFFAOYSA-N n,n-dimethylhexadecan-1-amine;hydrobromide Chemical compound [Br-].CCCCCCCCCCCCCCCC[NH+](C)C VHDPPDRSCMVFAV-UHFFFAOYSA-N 0.000 description 1
IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 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
150000001451 organic peroxides Chemical class 0.000 description 1
230000003647 oxidation Effects 0.000 description 1
238000007254 oxidation reaction Methods 0.000 description 1
NWVVVBRKAWDGAB-UHFFFAOYSA-N p-methoxyphenol Chemical group COC1=CC=C(O)C=C1 NWVVVBRKAWDGAB-UHFFFAOYSA-N 0.000 description 1
125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
229950010765 pivalate Drugs 0.000 description 1
IUGYQRQAERSCNH-UHFFFAOYSA-N pivalic acid Chemical compound CC(C)(C)C(O)=O IUGYQRQAERSCNH-UHFFFAOYSA-N 0.000 description 1
239000011120 plywood Substances 0.000 description 1
150000008442 polyphenolic compounds Chemical class 0.000 description 1
235000013824 polyphenols Nutrition 0.000 description 1
HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
150000003242 quaternary ammonium salts Chemical class 0.000 description 1
239000013558 reference substance Substances 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
238000007711 solidification Methods 0.000 description 1
230000008023 solidification Effects 0.000 description 1
239000002904 solvent Substances 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
239000000758 substrate Substances 0.000 description 1
125000000446 sulfanediyl group Chemical group *S* 0.000 description 1
239000004250 tert-Butylhydroquinone Substances 0.000 description 1
235000019281 tert-butylhydroquinone Nutrition 0.000 description 1
150000003573 thiols Chemical class 0.000 description 1
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
125000005590 trimellitic acid group Chemical group 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
CHJMFFKHPHCQIJ-UHFFFAOYSA-L zinc;octanoate Chemical compound [Zn+2].CCCCCCCC([O-])=O.CCCCCCCC([O-])=O CHJMFFKHPHCQIJ-UHFFFAOYSA-L 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
- C08G63/12—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
- C08G63/52—Polycarboxylic acids or polyhydroxy compounds in which at least one of the two components contains aliphatic unsaturation
- 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
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/02—Elements
- C08K3/08—Metals
- 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
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
- 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
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/24—Acids; Salts 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
- C09D167/06—Unsaturated polyesters having carbon-to-carbon unsaturation

Landscapes

Chemical & Material Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Life Sciences & Earth Sciences (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
Wood Science & Technology (AREA)
Macromonomer-Based Addition Polymer (AREA)
Polyesters Or Polycarbonates (AREA)

FI760947A 1975-04-10 1976-04-07 Foerfarande foer framstaellning av polyesterhartslack FI59806C (fi)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
FR7511199		1975-04-10
FR7511199A FR2307013A1 (fr)	1975-04-10	1975-04-10	Preparation de vernis a base de resine polyester

Publications (3)

Publication Number	Publication Date
FI760947A7 FI760947A7 (de)	1976-10-11
FI59806B FI59806B (fi)	1981-06-30
FI59806C true FI59806C (fi)	1981-10-12

Family

ID=9153742

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
FI760947A FI59806C (fi)	1975-04-10	1976-04-07	Foerfarande foer framstaellning av polyesterhartslack

Country Status (16)

Country	Link
US (1)	US4036908A (de)
AT (1)	AT351120B (de)
BE (1)	BE840613A (de)
CA (1)	CA1094724A (de)
DE (1)	DE2615370C3 (de)
DK (1)	DK166776A (de)
ES (1)	ES446806A1 (de)
FI (1)	FI59806C (de)
FR (1)	FR2307013A1 (de)
GB (1)	GB1523205A (de)
IE (1)	IE43131B1 (de)
IT (1)	IT1057511B (de)
NL (1)	NL7603790A (de)
NO (1)	NO761215L (de)
PT (1)	PT64992B (de)
SE (1)	SE404196B (de)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4277392A (en) *	1979-06-01	1981-07-07	Tenneco Chemicals, Inc.	Thickening agents for unsaturated polyester resin compositions
US4280979A (en) *	1979-09-18	1981-07-28	Union Carbide Corporation	Copolymers, compositions, and articles, and methods for making same
US4482701A (en) *	1981-10-17	1984-11-13	Nippon Paint Co., Ltd.	Hydrolyzable polyester resins, varnishes and coating compositions containing the same
CN105949971B (zh) *	2016-06-21	2018-05-29	上海长润发涂料有限公司	一种防变绿不饱和聚酯漆

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE1769309A1 (de) *	1968-05-16	1971-06-09	Lode Fa Emil	Verfahren zum Herstellen transparenter,klarer Polyesterpressteile
US3657387A (en) *	1970-04-29	1972-04-18	Grace W R & Co	Polyester resin composition with a long shelf life
FR2097513A5 (de) *	1970-07-09	1972-03-03	Renault
US3957906A (en) *	1971-12-10	1976-05-18	Koppers Company, Inc.	Chemically resistant polyester resins compositions
US3914200A (en) *	1972-01-27	1975-10-21	Ferro Corp	Rigid thermosetting load bearing compositions
JPS5029953B2 (de) *	1972-08-31	1975-09-27
US3804799A (en) *	1972-09-01	1974-04-16	Air Prod & Chem	Metal-amine complex accelerator for polyester resin curing
DE2311395C3 (de) *	1973-03-08	1983-12-22	Basf Ag, 6700 Ludwigshafen	Herstellung beschleunigt eindickender härtbarer Polyesterformmassen

1975
- 1975-04-10 FR FR7511199A patent/FR2307013A1/fr active Granted
1976
- 1976-02-27 SE SE7602696A patent/SE404196B/xx unknown
- 1976-03-08 ES ES446806A patent/ES446806A1/es not_active Expired
- 1976-03-19 US US05/668,722 patent/US4036908A/en not_active Expired - Lifetime
- 1976-04-07 FI FI760947A patent/FI59806C/fi not_active IP Right Cessation
- 1976-04-08 DK DK166776A patent/DK166776A/da not_active IP Right Cessation
- 1976-04-08 NO NO761215A patent/NO761215L/no unknown
- 1976-04-08 PT PT64992A patent/PT64992B/pt unknown
- 1976-04-08 GB GB14435/76A patent/GB1523205A/en not_active Expired
- 1976-04-08 DE DE2615370A patent/DE2615370C3/de not_active Expired
- 1976-04-09 IE IE745/76A patent/IE43131B1/en unknown
- 1976-04-09 IT IT48960/76A patent/IT1057511B/it active
- 1976-04-09 NL NL7603790A patent/NL7603790A/xx not_active Application Discontinuation
- 1976-04-09 AT AT263776A patent/AT351120B/de not_active IP Right Cessation
- 1976-04-09 CA CA249,968A patent/CA1094724A/en not_active Expired
- 1976-04-09 BE BE166042A patent/BE840613A/xx unknown

Also Published As

Publication number	Publication date
DE2615370A1 (de)	1976-10-21
ATA263776A (de)	1978-12-15
FI59806B (fi)	1981-06-30
PT64992A (fr)	1976-05-01
ES446806A1 (es)	1977-06-01
AT351120B (de)	1979-07-10
FR2307013B1 (de)	1977-11-10
GB1523205A (en)	1978-08-31
NO761215L (de)	1976-10-12
IE43131L (en)	1976-10-10
US4036908A (en)	1977-07-19
DE2615370B2 (de)	1979-04-19
NL7603790A (nl)	1976-10-12
DE2615370C3 (de)	1980-08-21
SE404196B (sv)	1978-09-25
DK166776A (da)	1976-10-11
PT64992B (fr)	1977-09-08
FI760947A7 (de)	1976-10-11
BE840613A (fr)	1976-10-11
IE43131B1 (en)	1980-12-31
SE7602696L (sv)	1976-10-11
IT1057511B (it)	1982-03-30
FR2307013A1 (fr)	1976-11-05
CA1094724A (en)	1981-01-27

Legal Events

Date	Code	Title	Description
2004-08-31	MM	Patent lapsed	Owner name: RHONE- POULENC INDUSTRIES

Publication	Publication Date	Title
CN103443184B (zh)	2016-02-17	用于固化树脂的促进剂
DE3612442A1 (de)	1987-10-22	Verfahren zur herstellung von uv-gehaerteten deckend pigmentierten beschichtungen
TW201245255A (en)	2012-11-16	Accelerator for curing resins
CN104583291A (zh)	2015-04-29	用于固化树脂的铁基加速剂
TW200904842A (en)	2009-02-01	Accelerator solution
US2951823A (en)	1960-09-06	Unsaturated polyesters of unsaturated alpha, beta-dicarboxylic acids and polyvalent alcohols
US4112146A (en)	1978-09-05	Polyester resin compositions which are photocurable in the presence of oxygen and an organic hydrazone polymerization initiator
US4175064A (en)	1979-11-20	Accelerator systems for the peroxide-catalyzed curing of unsaturated polyester resin compositions
FI59806B (fi)	1981-06-30	Foerfarande foer framstaellning av polyesterhartslack
US4042646A (en)	1977-08-16	Process for curing unsaturated resins
US4001348A (en)	1977-01-04	Unsaturated polyester resins containing additional accelerators
GB2051093A (en)	1981-01-14	Accelerated hardening of unsaturated polyester resins
CN1296353C (zh)	2007-01-24	甲基·丙基酮过氧化物制剂及其在固化不饱和聚酯树脂的方法中的用途
US4046740A (en)	1977-09-06	Novel polyester compositions
US3061580A (en)	1962-10-30	Unsaturated polyester resins containing a lithium halide as stabilizer and method ofmaking
JPH09302046A (ja)	1997-11-25	不飽和ポリエステル樹脂組成物、硬化物の製造法および成形材料
JPH09309936A (ja)	1997-12-02	不飽和ポリエステル樹脂組成物、硬化物の製造法および成形材料
US5451556A (en)	1995-09-19	Ammonium salt polymerization cocatalysts
SU326776A1 (ru)		Фотополимеризуемый состав
US3535404A (en)	1970-10-20	Unsaturated polyester resins containing tetracarboxylic acids or dianhydrides
JPH0454689B2 (de)	1992-09-01
JPH04372649A (ja)	1992-12-25	不飽和ポリエステル樹脂組成物、硬化物の製造法および成形材料
SU651710A3 (ru)	1979-03-05	Состав дл покрытий
JPH10212331A (ja)	1998-08-11	パーオキサイド組成物
JPH0414703B2 (de)	1992-03-13