CN117143396A

CN117143396A - 颗粒状紫外线吸收剂和树脂组合物

颗粒状紫外线吸收剂和树脂组合物 Download PDF

Info

Publication number: CN117143396A
Authority: CN; China
Prior art keywords: carbon atoms; group; alkyl group; branched alkyl; substituted
Prior art date: 2018-03-30
Legal status : Pending

Application number

CN202310961941.0A

Other languages

English (en)

Chinese (zh)

Inventor

石间洋辅

大森宏平

Current Assignee

Adeka Corp

Original Assignee

Adeka Corp

Priority date

2018-03-30

Filing date

2019-03-25

Publication date

2023-12-01

2019-03-25 Application filed by Adeka Corp filed Critical Adeka Corp

2023-12-01 Publication of CN117143396A publication Critical patent/CN117143396A/zh

Status Pending legal-status Critical Current

Links

239000006097 ultraviolet radiation absorber Substances 0.000 title claims abstract description 88
239000011342 resin composition Substances 0.000 title claims description 31
-1 triazine compound Chemical class 0.000 claims abstract description 216
239000002245 particle Substances 0.000 claims abstract description 54
238000009826 distribution Methods 0.000 claims abstract description 24
230000001186 cumulative effect Effects 0.000 claims abstract description 14
125000004432 carbon atom Chemical group C* 0.000 claims description 124
125000000217 alkyl group Chemical group 0.000 claims description 54
150000001875 compounds Chemical class 0.000 claims description 43
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 28
125000003118 aryl group Chemical group 0.000 claims description 18
125000003342 alkenyl group Chemical group 0.000 claims description 15
238000000634 powder X-ray diffraction Methods 0.000 claims description 15
238000004458 analytical method Methods 0.000 claims description 14
229920003002 synthetic resin Polymers 0.000 claims description 14
239000000057 synthetic resin Substances 0.000 claims description 14
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims description 13
125000002947 alkylene group Chemical group 0.000 claims description 12
125000003545 alkoxy group Chemical group 0.000 claims description 11
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 11
125000002877 alkyl aryl group Chemical group 0.000 claims description 10
125000000753 cycloalkyl group Chemical group 0.000 claims description 10
JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical group C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 claims description 9
125000003710 aryl alkyl group Chemical group 0.000 claims description 9
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 9
229910052717 sulfur Inorganic materials 0.000 claims description 9
125000005843 halogen group Chemical group 0.000 claims description 8
125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 claims description 8
229910052799 carbon Inorganic materials 0.000 claims description 7
229940124543 ultraviolet light absorber Drugs 0.000 claims description 7
239000011203 carbon fibre reinforced carbon Substances 0.000 claims description 6
238000000691 measurement method Methods 0.000 claims description 6
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 5
125000001424 substituent group Chemical group 0.000 claims description 3
125000004430 oxygen atom Chemical group O* 0.000 claims description 2
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 2
150000001335 aliphatic alkanes Chemical class 0.000 claims 1
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230000000052 comparative effect Effects 0.000 description 9
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LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 9
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238000002834 transmittance Methods 0.000 description 8
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238000002441 X-ray diffraction Methods 0.000 description 7
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XCJYREBRNVKWGJ-UHFFFAOYSA-N copper(II) phthalocyanine Chemical compound [Cu+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 XCJYREBRNVKWGJ-UHFFFAOYSA-N 0.000 description 7
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238000005469 granulation Methods 0.000 description 7
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125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 6
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125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 5
125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 5
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JFNLZVQOOSMTJK-KNVOCYPGSA-N norbornene Chemical compound C1[C@@H]2CC[C@H]1C=C2 JFNLZVQOOSMTJK-KNVOCYPGSA-N 0.000 description 5
125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 5
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 5
229940116351 sebacate Drugs 0.000 description 5
CXMXRPHRNRROMY-UHFFFAOYSA-L sebacate(2-) Chemical compound [O-]C(=O)CCCCCCCCC([O-])=O CXMXRPHRNRROMY-UHFFFAOYSA-L 0.000 description 5
125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 5
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239000002904 solvent Substances 0.000 description 5
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KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
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125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 4
CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 4
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125000001973 tert-pentyl group Chemical group [H]C([H])([H])C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 4
QGKMIGUHVLGJBR-UHFFFAOYSA-M (4z)-1-(3-methylbutyl)-4-[[1-(3-methylbutyl)quinolin-1-ium-4-yl]methylidene]quinoline;iodide Chemical compound [I-].C12=CC=CC=C2N(CCC(C)C)C=CC1=CC1=CC=[N+](CCC(C)C)C2=CC=CC=C12 QGKMIGUHVLGJBR-UHFFFAOYSA-M 0.000 description 3
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125000002704 decyl group Chemical group [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])* 0.000 description 3
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125000000040 m-tolyl group Chemical group [H]C1=C([H])C(*)=C([H])C(=C1[H])C([H])([H])[H] 0.000 description 3
VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 3
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AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 3
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XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 3
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125000001989 1,3-phenylene group Chemical group [H]C1=C([H])C([*:1])=C([H])C([*:2])=C1[H] 0.000 description 2
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ULQISTXYYBZJSJ-UHFFFAOYSA-N 12-hydroxyoctadecanoic acid Chemical compound CCCCCCC(O)CCCCCCCCCCC(O)=O ULQISTXYYBZJSJ-UHFFFAOYSA-N 0.000 description 2
238000005160 1H NMR spectroscopy Methods 0.000 description 2
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