BR0309389B1 - Processos para cura de uma composição, substrato revestido, revestimento assim obtido, bem como processo para produção de moldagens de materiais compostos - Google Patents

Info

Publication number

BR0309389B1

BR0309389B1 BRPI0309389-1A BR0309389A BR0309389B1 BR 0309389 B1 BR0309389 B1 BR 0309389B1 BR 0309389 A BR0309389 A BR 0309389A BR 0309389 B1 BR0309389 B1 BR 0309389B1

Authority

BR

Brazil

Prior art keywords

alkyl

phenyl

compound

hydrogen

alkoxy

Prior art date

2002-04-19

Links

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• 238000000034 method Methods 0.000 title claims abstract description 88
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• -1 siloxane radical Chemical class 0.000 claims description 222
• 150000001875 compounds Chemical class 0.000 claims description 127
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 79
• 125000000217 alkyl group Chemical group 0.000 claims description 49
• 239000001257 hydrogen Substances 0.000 claims description 48
• 229910052739 hydrogen Inorganic materials 0.000 claims description 48
• 150000002431 hydrogen Chemical class 0.000 claims description 41
• 150000003254 radicals Chemical class 0.000 claims description 41
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• 238000006243 chemical reaction Methods 0.000 claims description 22
• 125000004430 oxygen atom Chemical group O* 0.000 claims description 21
• 239000000049 pigment Substances 0.000 claims description 19
• 239000000654 additive Substances 0.000 claims description 18
• 125000001624 naphthyl group Chemical group 0.000 claims description 17
• 229910052757 nitrogen Inorganic materials 0.000 claims description 17
• 230000009471 action Effects 0.000 claims description 16
• 125000003545 alkoxy group Chemical group 0.000 claims description 16
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 16
• 239000004593 Epoxy Substances 0.000 claims description 15
• 238000006068 polycondensation reaction Methods 0.000 claims description 14
• 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 13
• 229910052760 oxygen Inorganic materials 0.000 claims description 13
• 229920000877 Melamine resin Polymers 0.000 claims description 12
• 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 12
• 239000000975 dye Substances 0.000 claims description 12
• 125000004642 (C1-C12) alkoxy group Chemical group 0.000 claims description 11
• 125000004433 nitrogen atom Chemical group N* 0.000 claims description 11
• 238000010438 heat treatment Methods 0.000 claims description 10
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• 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 9
• 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 9
• 239000012949 free radical photoinitiator Substances 0.000 claims description 9
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• 125000001424 substituent group Chemical group 0.000 claims description 9
• 125000004400 (C1-C12) alkyl group Chemical group 0.000 claims description 8
• 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 8
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• 125000004432 carbon atom Chemical group C* 0.000 claims description 6
• 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 6
• 229910052717 sulfur Inorganic materials 0.000 claims description 6
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• 125000006710 (C2-C12) alkenyl group Chemical group 0.000 claims description 4
• 125000004390 alkyl sulfonyl group Chemical group 0.000 claims description 4
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• 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 4
• 229910052801 chlorine Inorganic materials 0.000 claims description 4
• 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 4
• 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 4
• 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 claims description 4
• 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 4
• 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims description 4
• 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims description 3
• 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims description 3
• 125000003860 C1-C20 alkoxy group Chemical group 0.000 claims description 3
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• 125000000753 cycloalkyl group Chemical group 0.000 claims description 3
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• GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 17
• 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 16
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