SE431460B - Forfarande for framstellning av ett for blandning med alifatiska dikarbonsyror till ett pulverlackbindemedel lempligt akrylharts med glycidylgrupper, samt anvendning av hartset - Google Patents

Forfarande for framstellning av ett for blandning med alifatiska dikarbonsyror till ett pulverlackbindemedel lempligt akrylharts med glycidylgrupper, samt anvendning av hartset

Info

Publication number: SE431460B
Authority: SE; Sweden
Prior art keywords: weight; parts; mixture; powder coating; acrylic resin
Prior art date: 1977-11-05

Application number

SE7811417A

Other languages

English (en)

Swedish (sv)

Other versions

SE7811417L (sv

Inventor

H-J Holle

G Morlock

Original Assignee

Degussa

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.)

1977-11-05

Filing date

1978-11-03

Publication date

1984-02-06

1978-11-03 Application filed by Degussa filed Critical Degussa

1979-05-06 Publication of SE7811417L publication Critical patent/SE7811417L/xx

1984-02-06 Publication of SE431460B publication Critical patent/SE431460B/sv

Links

239000000203 mixture Substances 0.000 title claims description 46
239000011248 coating agent Substances 0.000 title claims description 34
239000004925 Acrylic resin Substances 0.000 title claims description 30
229920000178 Acrylic resin Polymers 0.000 title claims description 30
238000000034 method Methods 0.000 title claims description 22
238000002360 preparation method Methods 0.000 title claims description 10
LBVWYGNGGJURHQ-UHFFFAOYSA-N dicarbon Chemical class [C-]#[C+] LBVWYGNGGJURHQ-UHFFFAOYSA-N 0.000 title 1
SGFJJNBUMXQSMU-PDBXOOCHSA-N oxiran-2-ylmethyl (9z,12z,15z)-octadeca-9,12,15-trienoate Chemical group CC\C=C/C\C=C/C\C=C/CCCCCCCC(=O)OCC1CO1 SGFJJNBUMXQSMU-PDBXOOCHSA-N 0.000 title 1
239000000843 powder Substances 0.000 claims description 65
238000000576 coating method Methods 0.000 claims description 44
238000006116 polymerization reaction Methods 0.000 claims description 23
239000000178 monomer Substances 0.000 claims description 22
-1 aliphatic dicarboxylic acids Chemical class 0.000 claims description 21
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 18
125000004432 carbon atom Chemical group C* 0.000 claims description 14
150000002148 esters Chemical class 0.000 claims description 13
VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims description 12
VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 claims description 11
239000011230 binding agent Substances 0.000 claims description 10
229910000147 aluminium phosphate Inorganic materials 0.000 claims description 9
RPQRDASANLAFCM-UHFFFAOYSA-N oxiran-2-ylmethyl prop-2-enoate Chemical compound C=CC(=O)OCC1CO1 RPQRDASANLAFCM-UHFFFAOYSA-N 0.000 claims description 6
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 5
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 4
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 4
125000001931 aliphatic group Chemical group 0.000 claims description 4
125000003710 aryl alkyl group Chemical group 0.000 claims description 4
125000003118 aryl group Chemical group 0.000 claims description 4
239000003054 catalyst Substances 0.000 claims description 4
230000009477 glass transition Effects 0.000 claims description 4
125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 claims description 4
229920001519 homopolymer Polymers 0.000 claims description 4
238000002156 mixing Methods 0.000 claims description 4
229910052799 carbon Inorganic materials 0.000 claims description 2
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 2
229920002554 vinyl polymer Polymers 0.000 claims description 2
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 27
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 26
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 24
239000000155 melt Substances 0.000 description 17
ZQMIGQNCOMNODD-UHFFFAOYSA-N diacetyl peroxide Chemical compound CC(=O)OOC(C)=O ZQMIGQNCOMNODD-UHFFFAOYSA-N 0.000 description 16
DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 16
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 15
CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 12
239000004922 lacquer Substances 0.000 description 11
229910000831 Steel Inorganic materials 0.000 description 10
229910052751 metal Inorganic materials 0.000 description 10
239000002184 metal Substances 0.000 description 10
239000010959 steel Substances 0.000 description 10
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
229920000642 polymer Polymers 0.000 description 9
238000005507 spraying Methods 0.000 description 9
239000004408 titanium dioxide Substances 0.000 description 9
SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 8
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 8
239000004698 Polyethylene Substances 0.000 description 8
CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 8
238000001816 cooling Methods 0.000 description 8
229960002380 dibutyl phthalate Drugs 0.000 description 8
239000011888 foil Substances 0.000 description 8
238000010438 heat treatment Methods 0.000 description 8
238000009863 impact test Methods 0.000 description 8
229920000573 polyethylene Polymers 0.000 description 8
239000000243 solution Substances 0.000 description 8
230000001960 triggered effect Effects 0.000 description 8
HVLLSGMXQDNUAL-UHFFFAOYSA-N triphenyl phosphite Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)OC1=CC=CC=C1 HVLLSGMXQDNUAL-UHFFFAOYSA-N 0.000 description 8
238000005452 bending Methods 0.000 description 7
238000006243 chemical reaction Methods 0.000 description 7
150000003839 salts Chemical class 0.000 description 7
239000007921 spray Substances 0.000 description 7
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 6
238000003860 storage Methods 0.000 description 6
PSYGHMBJXWRQFD-UHFFFAOYSA-N 2-(2-sulfanylacetyl)oxyethyl 2-sulfanylacetate Chemical compound SCC(=O)OCCOC(=O)CS PSYGHMBJXWRQFD-UHFFFAOYSA-N 0.000 description 5
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 5
239000002253 acid Substances 0.000 description 5
GNSFRPWPOGYVLO-UHFFFAOYSA-N 3-hydroxypropyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCO GNSFRPWPOGYVLO-UHFFFAOYSA-N 0.000 description 4
OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 4
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
150000001991 dicarboxylic acids Chemical class 0.000 description 4
BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 4
229920006395 saturated elastomer Polymers 0.000 description 4
239000000126 substance Substances 0.000 description 4
CWERGRDVMFNCDR-UHFFFAOYSA-N thioglycolic acid Chemical compound OC(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-N 0.000 description 4
GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 3
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
238000010304 firing Methods 0.000 description 3
230000009969 flowable effect Effects 0.000 description 3
239000000049 pigment Substances 0.000 description 3
HQHCYKULIHKCEB-UHFFFAOYSA-N tetradecanedioic acid Chemical compound OC(=O)CCCCCCCCCCCCC(O)=O HQHCYKULIHKCEB-UHFFFAOYSA-N 0.000 description 3
PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 2
OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 2
FRQQKWGDKVGLFI-UHFFFAOYSA-N 2-methylundecane-2-thiol Chemical compound CCCCCCCCCC(C)(C)S FRQQKWGDKVGLFI-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
VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
101100518501 Mus musculus Spp1 gene Proteins 0.000 description 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 2
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
150000008064 anhydrides Chemical class 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
150000001735 carboxylic acids Chemical class 0.000 description 2
150000001875 compounds Chemical class 0.000 description 2
BVXOPEOQUQWRHQ-UHFFFAOYSA-N dibutyl phosphite Chemical compound CCCCOP([O-])OCCCC BVXOPEOQUQWRHQ-UHFFFAOYSA-N 0.000 description 2
NMAKPIATXQEXBT-UHFFFAOYSA-N didecyl phenyl phosphite Chemical compound CCCCCCCCCCOP(OCCCCCCCCCC)OC1=CC=CC=C1 NMAKPIATXQEXBT-UHFFFAOYSA-N 0.000 description 2
GMSCBRSQMRDRCD-UHFFFAOYSA-N dodecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCOC(=O)C(C)=C GMSCBRSQMRDRCD-UHFFFAOYSA-N 0.000 description 2
239000007789 gas Substances 0.000 description 2
ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 2
TXXHDPDFNKHHGW-UHFFFAOYSA-N muconic acid Chemical compound OC(=O)C=CC=CC(O)=O TXXHDPDFNKHHGW-UHFFFAOYSA-N 0.000 description 2
WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 2
WLJVNTCWHIRURA-UHFFFAOYSA-N pimelic acid Chemical compound OC(=O)CCCCCC(O)=O WLJVNTCWHIRURA-UHFFFAOYSA-N 0.000 description 2
239000002685 polymerization catalyst Substances 0.000 description 2
YPFDHNVEDLHUCE-UHFFFAOYSA-N propane-1,3-diol Chemical compound OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 2
TYFQFVWCELRYAO-UHFFFAOYSA-N suberic acid Chemical compound OC(=O)CCCCCCC(O)=O TYFQFVWCELRYAO-UHFFFAOYSA-N 0.000 description 2
239000004094 surface-active agent Substances 0.000 description 2
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 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
WGKLOLBTFWFKOD-UHFFFAOYSA-N tris(2-nonylphenyl) phosphite Chemical compound CCCCCCCCCC1=CC=CC=C1OP(OC=1C(=CC=CC=1)CCCCCCCCC)OC1=CC=CC=C1CCCCCCCCC WGKLOLBTFWFKOD-UHFFFAOYSA-N 0.000 description 2
MPTYEIZAMRVIQN-UHFFFAOYSA-N (2-methyl-3-oxobutan-2-yl)sulfonyloxy 2-methyl-3-oxobutane-2-sulfonate Chemical compound CC(=O)C(C)(C)S(=O)(=O)OOS(=O)(=O)C(C)(C)C(C)=O MPTYEIZAMRVIQN-UHFFFAOYSA-N 0.000 description 1
229940058015 1,3-butylene glycol Drugs 0.000 description 1
KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 1
LGJCFVYMIJLQJO-UHFFFAOYSA-N 1-dodecylperoxydodecane Chemical compound CCCCCCCCCCCCOOCCCCCCCCCCCC LGJCFVYMIJLQJO-UHFFFAOYSA-N 0.000 description 1
NVZWEEGUWXZOKI-UHFFFAOYSA-N 1-ethenyl-2-methylbenzene Chemical compound CC1=CC=CC=C1C=C NVZWEEGUWXZOKI-UHFFFAOYSA-N 0.000 description 1
ZFFMLCVRJBZUDZ-UHFFFAOYSA-N 2,3-dimethylbutane Chemical group CC(C)C(C)C ZFFMLCVRJBZUDZ-UHFFFAOYSA-N 0.000 description 1
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WSFYPFLCEFLXOZ-UHFFFAOYSA-N 2-decylbutanedioic acid Chemical compound CCCCCCCCCCC(C(O)=O)CC(O)=O WSFYPFLCEFLXOZ-UHFFFAOYSA-N 0.000 description 1
FWWXYLGCHHIKNY-UHFFFAOYSA-N 2-ethoxyethyl prop-2-enoate Chemical compound CCOCCOC(=O)C=C FWWXYLGCHHIKNY-UHFFFAOYSA-N 0.000 description 1
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YXYJVFYWCLAXHO-UHFFFAOYSA-N 2-methoxyethyl 2-methylprop-2-enoate Chemical compound COCCOC(=O)C(C)=C YXYJVFYWCLAXHO-UHFFFAOYSA-N 0.000 description 1
HFCUBKYHMMPGBY-UHFFFAOYSA-N 2-methoxyethyl prop-2-enoate Chemical compound COCCOC(=O)C=C HFCUBKYHMMPGBY-UHFFFAOYSA-N 0.000 description 1
OELQSSWXRGADDE-UHFFFAOYSA-N 2-methylprop-2-eneperoxoic acid Chemical compound CC(=C)C(=O)OO OELQSSWXRGADDE-UHFFFAOYSA-N 0.000 description 1
RUMACXVDVNRZJZ-UHFFFAOYSA-N 2-methylpropyl 2-methylprop-2-enoate Chemical compound CC(C)COC(=O)C(C)=C RUMACXVDVNRZJZ-UHFFFAOYSA-N 0.000 description 1
229940090248 4-hydroxybenzoic acid Drugs 0.000 description 1
YKXAYLPDMSGWEV-UHFFFAOYSA-N 4-hydroxybutyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCCO YKXAYLPDMSGWEV-UHFFFAOYSA-N 0.000 description 1
NDWUBGAGUCISDV-UHFFFAOYSA-N 4-hydroxybutyl prop-2-enoate Chemical compound OCCCCOC(=O)C=C NDWUBGAGUCISDV-UHFFFAOYSA-N 0.000 description 1
NUXLDNTZFXDNBA-UHFFFAOYSA-N 6-bromo-2-methyl-4h-1,4-benzoxazin-3-one Chemical compound C1=C(Br)C=C2NC(=O)C(C)OC2=C1 NUXLDNTZFXDNBA-UHFFFAOYSA-N 0.000 description 1
BWDBEAQIHAEVLV-UHFFFAOYSA-N 6-methylheptan-1-ol Chemical compound CC(C)CCCCCO BWDBEAQIHAEVLV-UHFFFAOYSA-N 0.000 description 1
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 1
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
YIVJZNGAASQVEM-UHFFFAOYSA-N Lauroyl peroxide Chemical compound CCCCCCCCCCCC(=O)OOC(=O)CCCCCCCCCCC YIVJZNGAASQVEM-UHFFFAOYSA-N 0.000 description 1
239000004594 Masterbatch (MB) Substances 0.000 description 1
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239000004952 Polyamide Substances 0.000 description 1
ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
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239000002216 antistatic agent Substances 0.000 description 1
230000009286 beneficial effect Effects 0.000 description 1
ZKTGWOXVQUNCLN-UHFFFAOYSA-N bis(2-nonylphenyl) hydrogen phosphite Chemical compound CCCCCCCCCC1=CC=CC=C1OP(O)OC1=CC=CC=C1CCCCCCCCC ZKTGWOXVQUNCLN-UHFFFAOYSA-N 0.000 description 1
BMRWNKZVCUKKSR-UHFFFAOYSA-N butane-1,2-diol Chemical compound CCC(O)CO BMRWNKZVCUKKSR-UHFFFAOYSA-N 0.000 description 1
235000019437 butane-1,3-diol Nutrition 0.000 description 1
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
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238000000354 decomposition reaction Methods 0.000 description 1
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239000000945 filler Substances 0.000 description 1
239000000446 fuel Substances 0.000 description 1
239000001530 fumaric acid Substances 0.000 description 1
238000009499 grossing Methods 0.000 description 1
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230000014759 maintenance of location Effects 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
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125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
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150000002924 oxiranes Chemical class 0.000 description 1
239000003973 paint Substances 0.000 description 1
PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
150000002978 peroxides Chemical class 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
239000004033 plastic Substances 0.000 description 1
229920002647 polyamide Polymers 0.000 description 1
229920000647 polyepoxide Polymers 0.000 description 1
229920000728 polyester Polymers 0.000 description 1
229920000570 polyether Polymers 0.000 description 1
229920001223 polyethylene glycol Polymers 0.000 description 1
230000001105 regulatory effect Effects 0.000 description 1
239000011347 resin Substances 0.000 description 1
229920005989 resin Polymers 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
239000011734 sodium Substances 0.000 description 1
239000008247 solid mixture Substances 0.000 description 1
230000002459 sustained effect Effects 0.000 description 1
BWSZXUOMATYHHI-UHFFFAOYSA-N tert-butyl octaneperoxoate Chemical compound CCCCCCCC(=O)OOC(C)(C)C BWSZXUOMATYHHI-UHFFFAOYSA-N 0.000 description 1
UWHCKJMYHZGTIT-UHFFFAOYSA-N tetraethylene glycol Chemical compound OCCOCCOCCOCCO UWHCKJMYHZGTIT-UHFFFAOYSA-N 0.000 description 1
YHGNXQAFNHCBTK-OWOJBTEDSA-N trans-3-hexenedioic acid Chemical compound OC(=O)C\C=C\CC(O)=O YHGNXQAFNHCBTK-OWOJBTEDSA-N 0.000 description 1
XTTGYFREQJCEML-UHFFFAOYSA-N tributyl phosphite Chemical compound CCCCOP(OCCCC)OCCCC XTTGYFREQJCEML-UHFFFAOYSA-N 0.000 description 1
DXNCZXXFRKPEPY-UHFFFAOYSA-N tridecanedioic acid Chemical compound OC(=O)CCCCCCCCCCCC(O)=O DXNCZXXFRKPEPY-UHFFFAOYSA-N 0.000 description 1
150000005691 triesters Chemical class 0.000 description 1
ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
SOUMJMSHQYAQTP-UHFFFAOYSA-N trihydroxy-methyl-octyl-lambda5-phosphane Chemical compound CCCCCCCCP(C)(O)(O)O SOUMJMSHQYAQTP-UHFFFAOYSA-N 0.000 description 1
CYTQBVOFDCPGCX-UHFFFAOYSA-N trimethyl phosphite Chemical compound COP(OC)OC CYTQBVOFDCPGCX-UHFFFAOYSA-N 0.000 description 1
230000007306 turnover Effects 0.000 description 1
239000002966 varnish Substances 0.000 description 1
230000004580 weight loss Effects 0.000 description 1
238000004383 yellowing Methods 0.000 description 1

Classifications

- 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
- C08F220/00—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 a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/12—Esters of monohydric alcohols or phenols
- 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
- C08F220/00—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 a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/12—Esters of monohydric alcohols or phenols
- C08F220/14—Methyl esters, e.g. methyl (meth)acrylate
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D133/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
- C09D133/04—Homopolymers or copolymers of esters
- C09D133/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
- C09D133/10—Homopolymers or copolymers of methacrylic acid esters
- C09D133/12—Homopolymers or copolymers of methyl methacrylate
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31678—Of metal
- Y10T428/31692—Next to addition polymer from unsaturated monomers
- Y10T428/31699—Ester, halide or nitrile of addition polymer
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31855—Of addition polymer from unsaturated monomers

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Polymers & Plastics (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Materials Engineering (AREA)
Wood Science & Technology (AREA)
Engineering & Computer Science (AREA)
Life Sciences & Earth Sciences (AREA)
Paints Or Removers (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Polymerisation Methods In General (AREA)

SE7811417A 1977-11-05 1978-11-03 Forfarande for framstellning av ett for blandning med alifatiska dikarbonsyror till ett pulverlackbindemedel lempligt akrylharts med glycidylgrupper, samt anvendning av hartset SE431460B (sv)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE2749576A DE2749576C3 (de)	1977-11-05	1977-11-05	Verfahren zur Herstellung eines Glycidylgruppen aufweisenden Acrylharzes und dessen Verwendung

Publications (2)

Publication Number	Publication Date
SE7811417L SE7811417L (sv)	1979-05-06
SE431460B true SE431460B (sv)	1984-02-06

Family

ID=6023095

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SE7811417A SE431460B (sv)	1977-11-05	1978-11-03	Forfarande for framstellning av ett for blandning med alifatiska dikarbonsyror till ett pulverlackbindemedel lempligt akrylharts med glycidylgrupper, samt anvendning av hartset

Country Status (11)

Country	Link
US (1)	US4181642A (fr)
JP (1)	JPS5474892A (fr)
AT (1)	ATA786078A (fr)
BE (1)	BE871776A (fr)
CH (1)	CH638820A5 (fr)
DE (1)	DE2749576C3 (fr)
FR (1)	FR2407943A1 (fr)
GB (1)	GB2007687B (fr)
IT (1)	IT7851768A0 (fr)
NL (1)	NL7808928A (fr)
SE (1)	SE431460B (fr)

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DE19752759A1 (de)	1997-11-28	1999-07-01	Basf Coatings Ag	Triboelektrisch aufladbare Pulverlacke
EP1084199A2 (fr)	1998-04-01	2001-03-21	BASF Coatings AG	Dispersion-vernis en poudre stabilisee de maniere non ionique
DE19835206A1 (de)	1998-08-04	2000-02-17	Basf Coatings Ag	Wäßrige Pulverklarlack-Dispersion
DE19841408C2 (de)	1998-09-10	2001-02-15	Basf Coatings Ag	Pulverklarlack und wäßrige Pulverklarlack-Slurry sowie deren Verwendung
DE19846650A1 (de)	1998-10-09	2000-04-13	Basf Coatings Ag	Pulverlack-Slurry mit mikroverkapselten Partikeln, ihre Herstellung und ihre Verwendung
DE19850211C1 (de)	1998-10-31	2000-11-23	Basf Coatings Ag	Pulverlacke und ihre Verwendung zur Herstellung geräuscharmer Pulverlackbeschichtungen
DE19908018A1 (de)	1999-02-25	2000-08-31	Basf Coatings Ag	Thermisch und mit aktinischer Strahlung härtbare Pulverslurry, Verfahren zu ihrer Herstellung und ihre Verwendung
DE19908013A1 (de)	1999-02-25	2000-08-31	Basf Coatings Ag	Mit aktinischer Strahlung und gegebenenfalls themisch härtbare Pulverslurrys, Verfahren zu ihrer Herstellung und ihre Verwendung
EP1163303B1 (fr)	1999-02-25	2004-06-16	BASF Coatings AG	Utilisation de tricyclodecane dimethanol pour la production de peintures multicouches
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US6360974B1 (en)	1999-05-19	2002-03-26	Basf Corporation	Powder slurry coating composition
DE10010405A1 (de) *	2000-03-03	2001-09-13	Basf Coatings Ag	Wäßrige (Meth)Acrylatcopolymerisat-Dispersionen, Verfahren zu ihrer Herstellung und ihre Verwendung
DE10126651A1 (de)	2001-06-01	2002-12-12	Basf Coatings Ag	Pulverlacksuspensionen (Pulverslurries) und Pulverlacke, Verfahren zu ihrer Herstellung und ihre Verwendung
US20040030176A1 (en) *	2001-09-05	2004-02-12	Ohrbom Walter H.	Gamma hydroxy carbamate compounds and method of making and using the same
DE10328663A1 (de) *	2003-06-26	2005-01-13	Bayer Materialscience Ag	Polyisocyanat-modifizierte Polycarbonsäuren
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DE10353638A1 (de)	2003-11-17	2005-06-23	Basf Coatings Ag	Strukturviskose, wässrige Dispersionen, Verfahren zu ihrer Herstellung und ihre Verwendung
US20060078740A1 (en) *	2004-10-07	2006-04-13	Zern John R	Barrier coatings
US7390858B2 (en) *	2005-10-18	2008-06-24	Valspar Sourcing, Inc.	Coating compositions and methods
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JP5689172B2 (ja)	2010-06-15	2015-03-25	ビーエーエスエフソシエタス・ヨーロピアＢａｓｆＳｅ	エポキシ樹脂組成物中での環状カーボネートの使用
US8586653B2 (en)	2011-09-19	2013-11-19	Basf Se	Curing of epoxy resin compositions comprising cyclic carbonates using mixtures of amino hardeners
WO2013041398A1 (fr)	2011-09-19	2013-03-28	Basf Se	Durcissement de compositions de résine époxy contenant des carbonates cycliques avec des mélanges de durcisseurs amines
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US8877837B2 (en)	2011-09-21	2014-11-04	Basf Se	Curing of epoxy resin compositions comprising cyclic carbonates using mixtures of amino hardeners and catalysts
DK2764033T3 (en)	2011-10-04	2015-09-14	Basf Se	EPOXIDHARPIKSSAMMENSÆTNINGER CONTAINING A 2-OXO [1,3] dioxolane
US20160208042A1 (en)	2013-10-01	2016-07-21	Basf Se	Multi-component epoxy resin composition
DE102014006519A1 (de)	2014-05-03	2015-11-05	Smart Material Printing B.V.	Verwendung magnetischer und/oder magnetisierbarer, polymerer Mikro- und/oder Nanocomposite zur Herstellung komplexer, magnetischer und/oder magnetisierbarer Formteile mithilfe additiver Fabrikatoren
DE102015000814A1 (de)	2015-01-21	2016-07-21	Smart Material Printing B.V.	Biozide Ausrüstung von Gegenständen mit Polyoxometallat-Mikro- und/oder -Nanopartikeln
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US3525721A (en) *	1967-11-14	1970-08-25	Goodrich Co B F	Copolymers of alkoxy alkyl acrylates,alkyl acrylates and glycidyl acrylate
US3845010A (en) *	1971-12-17	1974-10-29	Ford Motor Co	Thermoset molding powders employing glycidyl methacrylate functional polymer and dibasic acid crosslinking agent and moldings thereof
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JPS51125115A (en) *	1974-11-11	1976-11-01	Dainippon Ink & Chem Inc	Thermosetting resin composition for use in powder coating

1977
- 1977-11-05 DE DE2749576A patent/DE2749576C3/de not_active Expired
1978
- 1978-08-30 NL NL7808928A patent/NL7808928A/xx not_active Application Discontinuation
- 1978-09-13 FR FR7826250A patent/FR2407943A1/fr active Granted
- 1978-09-25 US US05/946,059 patent/US4181642A/en not_active Expired - Lifetime
- 1978-10-13 GB GB7840484A patent/GB2007687B/en not_active Expired
- 1978-11-02 JP JP13461178A patent/JPS5474892A/ja active Granted
- 1978-11-03 IT IT7851768A patent/IT7851768A0/it unknown
- 1978-11-03 AT AT0786078A patent/ATA786078A/de not_active Application Discontinuation
- 1978-11-03 SE SE7811417A patent/SE431460B/sv unknown
- 1978-11-03 BE BE6046659A patent/BE871776A/fr not_active IP Right Cessation
- 1978-11-06 CH CH1141078A patent/CH638820A5/de not_active IP Right Cessation

Also Published As

Publication number	Publication date
ATA786078A (de)	1985-09-15
FR2407943B1 (fr)	1982-10-22
US4181642A (en)	1980-01-01
NL7808928A (nl)	1979-05-08
SE7811417L (sv)	1979-05-06
GB2007687B (en)	1982-05-12
JPS5474892A (en)	1979-06-15
CH638820A5 (de)	1983-10-14
FR2407943A1 (fr)	1979-06-01
DE2749576B2 (de)	1979-08-16
IT7851768A0 (it)	1978-11-03
DE2749576A1 (de)	1979-05-17
BE871776A (fr)	1979-05-03
DE2749576C3 (de)	1980-04-24
GB2007687A (en)	1979-05-23
JPS5523852B2 (fr)	1980-06-25

Publication	Publication Date	Title
SE431460B (sv)	1984-02-06	Forfarande for framstellning av ett for blandning med alifatiska dikarbonsyror till ett pulverlackbindemedel lempligt akrylharts med glycidylgrupper, samt anvendning av hartset
KR101291437B1 (ko)	2013-07-31	수성 바인더 라텍스의 제조 방법
US4313861A (en)	1982-02-02	Latex autodeposition coatings
EP1789486A1 (fr)	2007-05-30	Compositions de revetement a stabilite amelioree
US9221992B2 (en)	2015-12-29	Aqueous coating compositions
JPH08504232A (ja)	1996-05-07	変性された塩素化ポリオレフィン、それらの水性分散体、およびコーティング組成物におけるそれらの使用
US3926888A (en)	1975-12-16	Method of making aqueous coating compositions of acrylic polymer latex, acrylic polymer solution, aminoplast and acrylic stabilizer polymer
KR960005429B1 (ko)	1996-04-25	열경화성 분체 도료용 조성물
US4380601A (en)	1983-04-19	Thermosetting catonic acrylic latices and their use in coating compositions
US7282531B2 (en)	2007-10-16	Acrylic resin composition dispersed in water
CA2196796A1 (fr)	1996-12-12	Composition thermodurcissable, methode d'obtention d'un revetement de f nition et articles connexes
AU626959B2 (en)	1992-08-13	Phosphorous-containing polymer compositions comprising water-soluble polyvalent metal compounds
WO2001097984A2 (fr)	2001-12-27	Procede d'application d'un revetement sur des substrats metalliques nus non traites
JPS6131124B2 (fr)	1986-07-18
JP7274534B2 (ja)	2023-05-16	塗料組成物
US3694388A (en)	1972-09-26	Acrylic polymers
EP0170288A2 (fr)	1986-02-05	Additif pour améliorer la résistance aux intempéries et réduire la viscosité de revêtements contenant une grande quantité de matières solides
US3696063A (en)	1972-10-03	Thermosetting reflow resins of copolymers of alkyl methacrylates
CA2497035A1 (fr)	2004-11-18	Revetement, composition de revetement et procede permettant d'ameliorer l'adhesion du revetement
JPH03163179A (ja)	1991-07-15	溶剤型塗料組成物
JPS6187767A (ja)	1986-05-06	粉体塗料組成物
JPS5833268B2 (ja)	1983-07-19	フンマツヒフクザイ
JPH0347875A (ja)	1991-02-28	水性塗料組成物
JPH0726042B2 (ja)	1995-03-22	粉体塗料組成物
CA1067233A (fr)	1979-11-27	Methode de fabrication d'emails a base d'eau, sans agent tensio-actif