TWI646135B - 抗靜電液晶聚合物組合物 - Google Patents
抗靜電液晶聚合物組合物 Download PDFInfo
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- TWI646135B TWI646135B TW102137022A TW102137022A TWI646135B TW I646135 B TWI646135 B TW I646135B TW 102137022 A TW102137022 A TW 102137022A TW 102137022 A TW102137022 A TW 102137022A TW I646135 B TWI646135 B TW I646135B
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- polymer composition
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- polymer
- aromatic
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- 239000000203 mixture Substances 0.000 title claims abstract description 103
- 229920000106 Liquid crystal polymer Polymers 0.000 title claims abstract description 54
- 239000004977 Liquid-crystal polymers (LCPs) Substances 0.000 claims abstract description 51
- 239000002608 ionic liquid Substances 0.000 claims abstract description 26
- 239000011159 matrix material Substances 0.000 claims abstract description 14
- 229920000642 polymer Polymers 0.000 claims description 98
- -1 fatty acid carboxylate Chemical class 0.000 claims description 53
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 45
- 125000003118 aryl group Chemical group 0.000 claims description 36
- 238000012360 testing method Methods 0.000 claims description 33
- 239000000835 fiber Substances 0.000 claims description 29
- 238000002844 melting Methods 0.000 claims description 19
- 230000008018 melting Effects 0.000 claims description 19
- FJKROLUGYXJWQN-UHFFFAOYSA-N 4-hydroxybenzoic acid Chemical compound OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 claims description 16
- 239000000463 material Substances 0.000 claims description 15
- 150000003839 salts Chemical class 0.000 claims description 15
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 claims description 14
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 claims description 14
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 claims description 14
- 150000004060 quinone imines Chemical class 0.000 claims description 13
- 229910052751 metal Inorganic materials 0.000 claims description 12
- 239000002184 metal Substances 0.000 claims description 12
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 claims description 11
- VCCBEIPGXKNHFW-UHFFFAOYSA-N biphenyl-4,4'-diol Chemical compound C1=CC(O)=CC=C1C1=CC=C(O)C=C1 VCCBEIPGXKNHFW-UHFFFAOYSA-N 0.000 claims description 10
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 9
- 125000000217 alkyl group Chemical group 0.000 claims description 9
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 9
- 239000000194 fatty acid Substances 0.000 claims description 9
- 229930195729 fatty acid Natural products 0.000 claims description 9
- 239000000945 filler Substances 0.000 claims description 9
- 229940090248 4-hydroxybenzoic acid Drugs 0.000 claims description 8
- KAUQJMHLAFIZDU-UHFFFAOYSA-N 6-Hydroxy-2-naphthoic acid Chemical compound C1=C(O)C=CC2=CC(C(=O)O)=CC=C21 KAUQJMHLAFIZDU-UHFFFAOYSA-N 0.000 claims description 8
- 229920000049 Carbon (fiber) Polymers 0.000 claims description 8
- 125000003545 alkoxy group Chemical group 0.000 claims description 8
- 239000004917 carbon fiber Substances 0.000 claims description 8
- 125000002091 cationic group Chemical group 0.000 claims description 8
- 239000002557 mineral fiber Substances 0.000 claims description 8
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 7
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 7
- 125000001072 heteroaryl group Chemical group 0.000 claims description 7
- 239000002253 acid Substances 0.000 claims description 6
- 150000004982 aromatic amines Chemical class 0.000 claims description 6
- 125000000623 heterocyclic group Chemical group 0.000 claims description 6
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims description 6
- MHZGKXUYDGKKIU-UHFFFAOYSA-N Decylamine Chemical compound CCCCCCCCCCN MHZGKXUYDGKKIU-UHFFFAOYSA-N 0.000 claims description 5
- 125000003342 alkenyl group Chemical group 0.000 claims description 5
- 239000006229 carbon black Substances 0.000 claims description 5
- 229910002804 graphite Inorganic materials 0.000 claims description 5
- 239000010439 graphite Substances 0.000 claims description 5
- 125000001188 haloalkyl group Chemical group 0.000 claims description 5
- 150000002367 halogens Chemical class 0.000 claims description 5
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 claims description 4
- 125000004104 aryloxy group Chemical group 0.000 claims description 4
- 230000015572 biosynthetic process Effects 0.000 claims description 4
- 125000000000 cycloalkoxy group Chemical group 0.000 claims description 4
- 125000005553 heteroaryloxy group Chemical group 0.000 claims description 4
- 125000005844 heterocyclyloxy group Chemical group 0.000 claims description 4
- 125000001889 triflyl group Chemical group FC(F)(F)S(*)(=O)=O 0.000 claims description 4
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 claims description 3
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 3
- 125000003277 amino group Chemical group 0.000 claims description 3
- 150000003868 ammonium compounds Chemical class 0.000 claims description 3
- 229910052586 apatite Inorganic materials 0.000 claims description 3
- 150000001491 aromatic compounds Chemical class 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 239000001257 hydrogen Substances 0.000 claims description 3
- 150000002500 ions Chemical class 0.000 claims description 3
- 229960005489 paracetamol Drugs 0.000 claims description 3
- VSIIXMUUUJUKCM-UHFFFAOYSA-D pentacalcium;fluoride;triphosphate Chemical compound [F-].[Ca+2].[Ca+2].[Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O VSIIXMUUUJUKCM-UHFFFAOYSA-D 0.000 claims description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- 229910019142 PO4 Inorganic materials 0.000 claims description 2
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical compound OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 claims description 2
- 150000004645 aluminates Chemical class 0.000 claims description 2
- XLJMAIOERFSOGZ-UHFFFAOYSA-M cyanate Chemical compound [O-]C#N XLJMAIOERFSOGZ-UHFFFAOYSA-M 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 239000010452 phosphate Substances 0.000 claims description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 2
- ACVYVLVWPXVTIT-UHFFFAOYSA-M phosphinate Chemical compound [O-][PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-M 0.000 claims description 2
- 125000005496 phosphonium group Chemical group 0.000 claims description 2
- 239000000126 substance Substances 0.000 claims description 2
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 claims description 2
- HJHUXWBTVVFLQI-UHFFFAOYSA-N tributyl(methyl)azanium Chemical compound CCCC[N+](C)(CCCC)CCCC HJHUXWBTVVFLQI-UHFFFAOYSA-N 0.000 claims description 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 2
- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 claims 2
- GKNWQHIXXANPTN-UHFFFAOYSA-N 1,1,2,2,2-pentafluoroethanesulfonic acid Chemical compound OS(=O)(=O)C(F)(F)C(F)(F)F GKNWQHIXXANPTN-UHFFFAOYSA-N 0.000 claims 1
- 125000001475 halogen functional group Chemical group 0.000 claims 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims 1
- 229910052747 lanthanoid Inorganic materials 0.000 claims 1
- 150000002602 lanthanoids Chemical group 0.000 claims 1
- KYTZHLUVELPASH-UHFFFAOYSA-N naphthalene-1,2-dicarboxylic acid Chemical compound C1=CC=CC2=C(C(O)=O)C(C(=O)O)=CC=C21 KYTZHLUVELPASH-UHFFFAOYSA-N 0.000 claims 1
- RXOHFPCZGPKIRD-UHFFFAOYSA-L naphthalene-2,6-dicarboxylate Chemical compound C1=C(C([O-])=O)C=CC2=CC(C(=O)[O-])=CC=C21 RXOHFPCZGPKIRD-UHFFFAOYSA-L 0.000 claims 1
- 125000003396 thiol group Chemical group [H]S* 0.000 claims 1
- 230000003068 static effect Effects 0.000 abstract description 7
- 239000007788 liquid Substances 0.000 abstract description 6
- 238000010128 melt processing Methods 0.000 abstract description 4
- 238000000465 moulding Methods 0.000 abstract description 4
- 230000005611 electricity Effects 0.000 abstract description 2
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 18
- 238000006116 polymerization reaction Methods 0.000 description 17
- 238000000034 method Methods 0.000 description 14
- 239000000155 melt Substances 0.000 description 13
- 229910052799 carbon Inorganic materials 0.000 description 12
- 150000001875 compounds Chemical class 0.000 description 12
- 239000000523 sample Substances 0.000 description 11
- 239000007787 solid Substances 0.000 description 10
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 9
- 239000005711 Benzoic acid Substances 0.000 description 9
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 9
- 238000006243 chemical reaction Methods 0.000 description 9
- 239000011521 glass Substances 0.000 description 9
- 238000002156 mixing Methods 0.000 description 9
- 239000000178 monomer Substances 0.000 description 9
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
- 239000000314 lubricant Substances 0.000 description 8
- 239000000654 additive Substances 0.000 description 7
- 239000003365 glass fiber Substances 0.000 description 7
- 229910052757 nitrogen Inorganic materials 0.000 description 7
- 239000000758 substrate Substances 0.000 description 7
- 239000002585 base Substances 0.000 description 6
- 239000011231 conductive filler Substances 0.000 description 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 6
- RXOHFPCZGPKIRD-UHFFFAOYSA-N naphthalene-2,6-dicarboxylic acid Chemical compound C1=C(C(O)=O)C=CC2=CC(C(=O)O)=CC=C21 RXOHFPCZGPKIRD-UHFFFAOYSA-N 0.000 description 6
- 238000006146 oximation reaction Methods 0.000 description 6
- 239000002245 particle Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- ALKYHXVLJMQRLQ-UHFFFAOYSA-N 3-Hydroxy-2-naphthoate Chemical compound C1=CC=C2C=C(O)C(C(=O)O)=CC2=C1 ALKYHXVLJMQRLQ-UHFFFAOYSA-N 0.000 description 5
- 208000029618 autoimmune pulmonary alveolar proteinosis Diseases 0.000 description 5
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 5
- 239000003054 catalyst Substances 0.000 description 5
- 239000013068 control sample Substances 0.000 description 5
- 150000002148 esters Chemical class 0.000 description 5
- 239000010445 mica Substances 0.000 description 5
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- 238000006068 polycondensation reaction Methods 0.000 description 5
- 238000012545 processing Methods 0.000 description 5
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 5
- 239000004594 Masterbatch (MB) Substances 0.000 description 4
- 150000001412 amines Chemical class 0.000 description 4
- 238000004891 communication Methods 0.000 description 4
- 125000006612 decyloxy group Chemical group 0.000 description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 4
- 239000012765 fibrous filler Substances 0.000 description 4
- 239000007789 gas Substances 0.000 description 4
- 125000005843 halogen group Chemical group 0.000 description 4
- 238000003780 insertion Methods 0.000 description 4
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- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 4
- 239000001993 wax Substances 0.000 description 4
- JTGCXYYDAVPSFD-UHFFFAOYSA-N 4-(4-hydroxyphenyl)benzoic acid Chemical compound C1=CC(C(=O)O)=CC=C1C1=CC=C(O)C=C1 JTGCXYYDAVPSFD-UHFFFAOYSA-N 0.000 description 3
- JCJUKCIXTRWAQY-UHFFFAOYSA-N 6-hydroxynaphthalene-1-carboxylic acid Chemical compound OC1=CC=C2C(C(=O)O)=CC=CC2=C1 JCJUKCIXTRWAQY-UHFFFAOYSA-N 0.000 description 3
- 235000021355 Stearic acid Nutrition 0.000 description 3
- 230000006978 adaptation Effects 0.000 description 3
- 230000000996 additive effect Effects 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 3
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 3
- 239000002734 clay mineral Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 150000004665 fatty acids Chemical class 0.000 description 3
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 3
- 238000002347 injection Methods 0.000 description 3
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- 229910052500 inorganic mineral Inorganic materials 0.000 description 3
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- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 3
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- 239000004033 plastic Substances 0.000 description 3
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- HCNHNBLSNVSJTJ-UHFFFAOYSA-N 1,1-Bis(4-hydroxyphenyl)ethane Chemical compound C=1C=C(O)C=CC=1C(C)C1=CC=C(O)C=C1 HCNHNBLSNVSJTJ-UHFFFAOYSA-N 0.000 description 2
- URFNSYWAGGETFK-UHFFFAOYSA-N 1,2-bis(4-hydroxyphenyl)ethane Natural products C1=CC(O)=CC=C1CCC1=CC=C(O)C=C1 URFNSYWAGGETFK-UHFFFAOYSA-N 0.000 description 2
- LNETULKMXZVUST-UHFFFAOYSA-N 1-naphthoic acid Chemical compound C1=CC=C2C(C(=O)O)=CC=CC2=C1 LNETULKMXZVUST-UHFFFAOYSA-N 0.000 description 2
- JWAZRIHNYRIHIV-UHFFFAOYSA-N 2-naphthol Chemical compound C1=CC=CC2=CC(O)=CC=C21 JWAZRIHNYRIHIV-UHFFFAOYSA-N 0.000 description 2
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- WVDRSXGPQWNUBN-UHFFFAOYSA-N 4-(4-carboxyphenoxy)benzoic acid Chemical compound C1=CC(C(=O)O)=CC=C1OC1=CC=C(C(O)=O)C=C1 WVDRSXGPQWNUBN-UHFFFAOYSA-N 0.000 description 2
- NEQFBGHQPUXOFH-UHFFFAOYSA-N 4-(4-carboxyphenyl)benzoic acid Chemical group C1=CC(C(=O)O)=CC=C1C1=CC=C(C(O)=O)C=C1 NEQFBGHQPUXOFH-UHFFFAOYSA-N 0.000 description 2
- PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical compound NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 description 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
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- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
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- 125000001931 aliphatic group Chemical group 0.000 description 2
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- 150000008064 anhydrides Chemical class 0.000 description 2
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- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
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- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 2
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- HBGGXOJOCNVPFY-UHFFFAOYSA-N diisononyl phthalate Chemical compound CC(C)CCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCC(C)C HBGGXOJOCNVPFY-UHFFFAOYSA-N 0.000 description 2
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- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 2
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- FZZQNEVOYIYFPF-UHFFFAOYSA-N naphthalene-1,6-diol Chemical compound OC1=CC=CC2=CC(O)=CC=C21 FZZQNEVOYIYFPF-UHFFFAOYSA-N 0.000 description 2
- MNZMMCVIXORAQL-UHFFFAOYSA-N naphthalene-2,6-diol Chemical compound C1=C(O)C=CC2=CC(O)=CC=C21 MNZMMCVIXORAQL-UHFFFAOYSA-N 0.000 description 2
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- VGIBGUSAECPPNB-UHFFFAOYSA-L nonaaluminum;magnesium;tripotassium;1,3-dioxido-2,4,5-trioxa-1,3-disilabicyclo[1.1.1]pentane;iron(2+);oxygen(2-);fluoride;hydroxide Chemical compound [OH-].[O-2].[O-2].[O-2].[O-2].[O-2].[F-].[Mg+2].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[K+].[K+].[K+].[Fe+2].O1[Si]2([O-])O[Si]1([O-])O2.O1[Si]2([O-])O[Si]1([O-])O2.O1[Si]2([O-])O[Si]1([O-])O2.O1[Si]2([O-])O[Si]1([O-])O2.O1[Si]2([O-])O[Si]1([O-])O2.O1[Si]2([O-])O[Si]1([O-])O2.O1[Si]2([O-])O[Si]1([O-])O2 VGIBGUSAECPPNB-UHFFFAOYSA-L 0.000 description 1
- 229940067739 octyl sulfate Drugs 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-M oleate Chemical compound CCCCCCCC\C=C/CCCCCCCC([O-])=O ZQPPMHVWECSIRJ-KTKRTIGZSA-M 0.000 description 1
- 229940049964 oleate Drugs 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
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- 125000006340 pentafluoro ethyl group Chemical group FC(F)(F)C(F)(F)* 0.000 description 1
- YFSUTJLHUFNCNZ-UHFFFAOYSA-N perfluorooctane-1-sulfonic acid Chemical compound OS(=O)(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F YFSUTJLHUFNCNZ-UHFFFAOYSA-N 0.000 description 1
- SNGREZUHAYWORS-UHFFFAOYSA-N perfluorooctanoic acid Chemical compound OC(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F SNGREZUHAYWORS-UHFFFAOYSA-N 0.000 description 1
- 235000019271 petrolatum Nutrition 0.000 description 1
- PYOZTOXFQNWBIS-UHFFFAOYSA-N phenol;sodium Chemical compound [Na].OC1=CC=CC=C1 PYOZTOXFQNWBIS-UHFFFAOYSA-N 0.000 description 1
- UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 238000013001 point bending Methods 0.000 description 1
- 229920006267 polyester film Polymers 0.000 description 1
- 229920002098 polyfluorene Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 235000011056 potassium acetate Nutrition 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 125000002568 propynyl group Chemical group [*]C#CC([H])([H])[H] 0.000 description 1
- 125000003226 pyrazolyl group Chemical group 0.000 description 1
- 125000002098 pyridazinyl group Chemical group 0.000 description 1
- 125000004076 pyridyl group Chemical group 0.000 description 1
- 125000000714 pyrimidinyl group Chemical group 0.000 description 1
- 125000000168 pyrrolyl group Chemical group 0.000 description 1
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- BPILDHPJSYVNAF-UHFFFAOYSA-M sodium;diiodomethanesulfonate Chemical compound [Na+].[O-]S(=O)(=O)C(I)I BPILDHPJSYVNAF-UHFFFAOYSA-M 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- JIWBIWFOSCKQMA-UHFFFAOYSA-N stearidonic acid Natural products CCC=CCC=CCC=CCC=CCCCCC(O)=O JIWBIWFOSCKQMA-UHFFFAOYSA-N 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- UZZYXUGECOQHPU-UHFFFAOYSA-N sulfuric acid monooctyl ester Natural products CCCCCCCCOS(O)(=O)=O UZZYXUGECOQHPU-UHFFFAOYSA-N 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 1
- 125000000335 thiazolyl group Chemical group 0.000 description 1
- 125000001544 thienyl group Chemical group 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- 125000001425 triazolyl group Chemical group 0.000 description 1
- DXJLCRNXYNRGRA-UHFFFAOYSA-M tributyl(methyl)azanium;iodide Chemical compound [I-].CCCC[N+](C)(CCCC)CCCC DXJLCRNXYNRGRA-UHFFFAOYSA-M 0.000 description 1
- 235000013337 tricalcium citrate Nutrition 0.000 description 1
- ITMCEJHCFYSIIV-UHFFFAOYSA-M triflate Chemical compound [O-]S(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-M 0.000 description 1
- JFZKOODUSFUFIZ-UHFFFAOYSA-N trifluoro phosphate Chemical compound FOP(=O)(OF)OF JFZKOODUSFUFIZ-UHFFFAOYSA-N 0.000 description 1
- AEXDMFVPDVVSQJ-UHFFFAOYSA-N trifluoro(trifluoromethylsulfonyl)methane Chemical group FC(F)(F)S(=O)(=O)C(F)(F)F AEXDMFVPDVVSQJ-UHFFFAOYSA-N 0.000 description 1
- 150000004684 trihydrates Chemical class 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 239000003039 volatile agent Substances 0.000 description 1
- 235000019386 wax ester Nutrition 0.000 description 1
- 229910052724 xenon Inorganic materials 0.000 description 1
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 1
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 1
Classifications
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- 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
- C08K5/36—Sulfur-, selenium-, or tellurium-containing compounds
- C08K5/43—Compounds containing sulfur bound to nitrogen
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K19/00—Liquid crystal materials
- C09K19/04—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
- C09K19/38—Polymers
-
- 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
- C08K3/04—Carbon
-
- 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
- C08K5/16—Nitrogen-containing compounds
- C08K5/17—Amines; Quaternary ammonium compounds
- C08K5/19—Quaternary ammonium 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
- C08K7/00—Use of ingredients characterised by shape
- C08K7/02—Fibres or whiskers
- C08K7/04—Fibres or whiskers inorganic
- C08K7/06—Elements
-
- 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
- C08K7/00—Use of ingredients characterised by shape
- C08K7/02—Fibres or whiskers
- C08K7/04—Fibres or whiskers inorganic
- C08K7/10—Silicon-containing compounds
-
- 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
- C08L67/02—Polyesters derived from dicarboxylic acids and dihydroxy compounds
- C08L67/03—Polyesters derived from dicarboxylic acids and dihydroxy compounds the dicarboxylic acids and dihydroxy compounds having the carboxyl- and the hydroxy groups directly linked to aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K19/00—Liquid crystal materials
- C09K19/04—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
- C09K19/38—Polymers
- C09K19/3804—Polymers with mesogenic groups in the main chain
- C09K19/3809—Polyesters; Polyester derivatives, e.g. polyamides
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K19/00—Liquid crystal materials
- C09K19/52—Liquid crystal materials characterised by components which are not liquid crystals, e.g. additives with special physical aspect: solvents, solid particles
- C09K19/54—Additives having no specific mesophase characterised by their chemical composition
- C09K19/542—Macromolecular compounds
- C09K19/544—Macromolecular compounds as dispersing or encapsulating medium around the liquid crystal
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K19/00—Liquid crystal materials
- C09K19/52—Liquid crystal materials characterised by components which are not liquid crystals, e.g. additives with special physical aspect: solvents, solid particles
- C09K19/58—Dopants or charge transfer agents
- C09K19/582—Electrically active dopants, e.g. charge transfer agents
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- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B27/00—Optical systems or apparatus not provided for by any of the groups G02B1/00 - G02B26/00, G02B30/00
- G02B27/0006—Optical systems or apparatus not provided for by any of the groups G02B1/00 - G02B26/00, G02B30/00 with means to keep optical surfaces clean, e.g. by preventing or removing dirt, stains, contamination, condensation
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B7/00—Mountings, adjusting means, or light-tight connections, for optical elements
- G02B7/02—Mountings, adjusting means, or light-tight connections, for optical elements for lenses
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03B—APPARATUS OR ARRANGEMENTS FOR TAKING PHOTOGRAPHS OR FOR PROJECTING OR VIEWING THEM; APPARATUS OR ARRANGEMENTS EMPLOYING ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ACCESSORIES THEREFOR
- G03B17/00—Details of cameras or camera bodies; Accessories therefor
- G03B17/02—Bodies
- G03B17/12—Bodies with means for supporting objectives, supplementary lenses, filters, masks, or turrets
-
- H—ELECTRICITY
- H04—ELECTRIC COMMUNICATION TECHNIQUE
- H04N—PICTORIAL COMMUNICATION, e.g. TELEVISION
- H04N23/00—Cameras or camera modules comprising electronic image sensors; Control thereof
- H04N23/50—Constructional details
- H04N23/55—Optical parts specially adapted for electronic image sensors; Mounting thereof
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K19/00—Liquid crystal materials
- C09K19/52—Liquid crystal materials characterised by components which are not liquid crystals, e.g. additives with special physical aspect: solvents, solid particles
- C09K2019/521—Inorganic solid particles
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K19/00—Liquid crystal materials
- C09K19/52—Liquid crystal materials characterised by components which are not liquid crystals, e.g. additives with special physical aspect: solvents, solid particles
- C09K2019/528—Surfactants
Landscapes
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- General Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Signal Processing (AREA)
- Multimedia (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
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| US9284435B2 (en) * | 2012-10-16 | 2016-03-15 | Ticona Llc | Antistatic liquid crystalline polymer composition |
| WO2014088700A1 (en) | 2012-12-05 | 2014-06-12 | Ticona Llc | Conductive liquid crystalline polymer composition |
| CN111732821A (zh) | 2013-03-13 | 2020-10-02 | 提克纳有限责任公司 | 抗静电液晶聚合物组合物 |
| CN106164172B (zh) | 2014-04-09 | 2019-07-26 | 提克纳有限责任公司 | 摄像模组 |
| KR102305241B1 (ko) * | 2014-04-09 | 2021-09-24 | 티코나 엘엘씨 | 대전방지 중합체 조성물 |
| DE112016000328T5 (de) * | 2015-01-13 | 2017-10-19 | Ube Exsymo Co., Ltd. | Flexible Verbundplatte und mehrschichtige Leiterplatte |
| US9862809B2 (en) | 2015-07-31 | 2018-01-09 | Ticona Llc | Camera module |
| US10407605B2 (en) | 2015-07-31 | 2019-09-10 | Ticona Llc | Thermally conductive polymer composition |
| TWI708806B (zh) * | 2015-08-17 | 2020-11-01 | 美商堤康那責任有限公司 | 用於相機模組之液晶聚合物組合物 |
| CN107924039B (zh) * | 2015-09-01 | 2020-10-16 | 宝理塑料株式会社 | 照相机模块用液晶性树脂组合物及使用其的照相机模块 |
| US10633535B2 (en) | 2017-02-06 | 2020-04-28 | Ticona Llc | Polyester polymer compositions |
| WO2019109595A1 (en) * | 2017-12-05 | 2019-06-13 | Ticona Llc | Liquid crystalline polymer composition |
| KR102627886B1 (ko) | 2017-12-05 | 2024-01-19 | 티코나 엘엘씨 | 카메라 모듈에 사용하기 위한 방향족 중합체 조성물 |
| US11384238B2 (en) | 2018-02-08 | 2022-07-12 | Celanese Sales Germany Gmbh | Polymer composite containing recycled carbon fibers |
| EP3755515A4 (en) | 2018-02-20 | 2021-11-10 | Ticona LLC | THERMAL CONDUCTIVE POLYMER COMPOSITION |
| KR20210088555A (ko) * | 2018-11-09 | 2021-07-14 | 스미또모 가가꾸 가부시끼가이샤 | 액정 폴리에스테르 수지 조성물 및 성형품 |
| US11722759B2 (en) | 2019-03-20 | 2023-08-08 | Ticona Llc | Actuator assembly for a camera module |
| KR20210148198A (ko) | 2019-03-20 | 2021-12-07 | 티코나 엘엘씨 | 카메라 모듈에서 사용하기 위한 중합체 조성물 |
| CN110746754B (zh) * | 2019-09-25 | 2021-06-29 | 广东格瑞新材料股份有限公司 | 一种激光雕刻液晶高分子组合物及其制备方法 |
| CN115151403A (zh) | 2019-12-17 | 2022-10-04 | 提克纳有限责任公司 | 采用热致液晶聚合物的三维打印系统 |
| JP2023515975A (ja) * | 2020-02-26 | 2023-04-17 | ティコナ・エルエルシー | 電子デバイス |
| EP4110610A4 (en) * | 2020-02-26 | 2024-03-27 | Ticona LLC | POLYMER COMPOSITION FOR ELECTRONIC DEVICE |
| JP7737387B2 (ja) | 2020-02-26 | 2025-09-10 | ティコナ・エルエルシー | 回路構造体 |
| KR20220146567A (ko) * | 2020-02-26 | 2022-11-01 | 티코나 엘엘씨 | 전자 디바이스 |
| JP7744146B2 (ja) * | 2020-03-30 | 2025-09-25 | 日東電工株式会社 | 粘着剤組成物、粘着シート、及び接合体 |
| US11728065B2 (en) | 2020-07-28 | 2023-08-15 | Ticona Llc | Molded interconnect device |
| CN112126243B (zh) * | 2020-09-09 | 2022-06-07 | 金发科技股份有限公司 | 一种液晶聚合物组合物 |
| US20220127499A1 (en) * | 2020-10-26 | 2022-04-28 | Ticona Llc | Laminate Structure |
| EP4264742A1 (en) * | 2020-12-17 | 2023-10-25 | Ticona LLC | Antenna module for a 5g system |
| EP4263632A4 (en) | 2020-12-17 | 2024-11-20 | Ticona LLC | FIBER-REINFORCED PROPYLENE POLYMER COMPOSITION |
| US11728559B2 (en) | 2021-02-18 | 2023-08-15 | Ticona Llc | Polymer composition for use in an antenna system |
| US12209163B2 (en) | 2021-05-06 | 2025-01-28 | Ticona Llc | Polymer composition for use in a camera module |
| EP4095197A1 (en) * | 2021-05-28 | 2022-11-30 | SHPP Global Technologies B.V. | Articles and structures with colorable electro-static dissipative (esd) polycarbonate blends |
| CN118613966A (zh) | 2021-12-01 | 2024-09-06 | 提克纳有限责任公司 | 天线模块 |
| TW202340697A (zh) | 2021-12-13 | 2023-10-16 | 美商堤康那責任有限公司 | 樣品之滾珠凹部性質之測試技術 |
| US12421453B2 (en) * | 2022-08-22 | 2025-09-23 | Orbotech Ltd. | Cationic gettering in liquid crystal NCAP and PDLC films |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI230176B (en) * | 1999-10-06 | 2005-04-01 | 3M Innovative Properties Co | Antistatic composition |
| TW201235406A (en) * | 2010-11-30 | 2012-09-01 | Sumitomo Chemical Co | Liquid crystalline polyester composition |
Family Cites Families (132)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4161470A (en) | 1977-10-20 | 1979-07-17 | Celanese Corporation | Polyester of 6-hydroxy-2-naphthoic acid and para-hydroxy benzoic acid capable of readily undergoing melt processing |
| US4458039A (en) | 1983-02-07 | 1984-07-03 | Celanese Corporation | Thermotropic liquid crystalline polymer blend with reduced surface abrasion |
| JPS61285282A (ja) * | 1985-06-12 | 1986-12-16 | Polyplastics Co | 光伝送路接続端子組成物 |
| AU612707B2 (en) | 1987-10-12 | 1991-07-18 | Nippon Paint Co., Ltd. | Thermosetting polyester resin and powder coating resinous composition containing the same |
| US5928589A (en) | 1987-12-28 | 1999-07-27 | Teijin Limited | Processing for producing shaped wholly aromatic polyamide resin composition article and shaped article produced thereby |
| JP2830279B2 (ja) | 1989-05-11 | 1998-12-02 | 住友化学工業株式会社 | 流動性の改良された液晶ポリエステル樹脂組成物 |
| US5492946A (en) | 1990-06-04 | 1996-02-20 | Amoco Corporation | Liquid crystalline polymer blends and molded articles therefrom |
| US5204443A (en) | 1991-04-19 | 1993-04-20 | Hoechst Celanese Corp. | Melt processable poly(ester-amide) capable of forming an anisotropic melt containing an aromatic moiety capable of forming an amide linkage |
| TW340130B (en) | 1993-12-28 | 1998-09-11 | Toray Industries | Shaped article of liquid crystalline resin |
| US5830940A (en) | 1993-12-28 | 1998-11-03 | Toray Industries, Inc. | Shaped article of liquid crystalline polymer |
| KR100207568B1 (ko) | 1994-08-27 | 1999-07-15 | 손욱 | 전도성 측쇄형 액정화합물 및 이를 사용한 배향막 |
| US6492463B1 (en) | 1994-08-31 | 2002-12-10 | E. I. Du Pont De Nemours And Company | Liquid crystalline polymer composition |
| US5616680A (en) | 1994-10-04 | 1997-04-01 | Hoechst Celanese Corporation | Process for producing liquid crystal polymer |
| KR100366341B1 (ko) | 1994-10-18 | 2003-05-16 | 포리프라스치쿠스 가부시끼 가이샤 | 열가소성수지조성물,그사출성형방법및사출성형체 |
| EP0747422B1 (en) | 1995-06-09 | 2002-09-25 | Sumitomo Chemical Company Limited | Use of inorganic oxides or hydroxides in liquid crystalline polyester resins |
| US5691689A (en) * | 1995-08-11 | 1997-11-25 | Eaton Corporation | Electrical circuit protection devices comprising PTC conductive liquid crystal polymer compositions |
| US5962122A (en) | 1995-11-28 | 1999-10-05 | Hoechst Celanese Corporation | Liquid crystalline polymer composites having high dielectric constant |
| JP3686718B2 (ja) | 1995-12-27 | 2005-08-24 | ポリプラスチックス株式会社 | 液晶性ポリマー組成物および成形体 |
| DE69712551T3 (de) | 1996-02-19 | 2008-02-21 | Sumitomo Chemical Co. Ltd. | Flüssigkristalline Polyesterharz-Zusammensetzung |
| TW515822B (en) | 1997-01-31 | 2003-01-01 | Toray Industries | Liquid-crystalline resin composition and precision moldings of the composition |
| US6121369A (en) | 1997-06-06 | 2000-09-19 | Eastman Chemical Company | Liquid crystalline polyester compositions containing carbon black |
| US6046300A (en) | 1997-12-26 | 2000-04-04 | Toray Industries, Inc. | Liquid-crystalline resin and thermoplastic resin composition |
| US6294618B1 (en) | 1998-04-09 | 2001-09-25 | E. I. Du Pont De Nemours And Company | Low viscosity liquid crystalline polymer compositions |
| US6833405B1 (en) | 1998-07-31 | 2004-12-21 | E. I. Du Pont De Nemours And Company | Compositions containing liquid crystalline polymers |
| US5969083A (en) | 1998-09-18 | 1999-10-19 | Eastman Chemical Company | Liquid crystalline polyesters having a surprisingly good combination of a low melting point, a high heat distortion temperature, a low melt viscosity, and a high tensile elongation |
| TW490478B (en) | 1998-11-12 | 2002-06-11 | Sumitomo Chemical Co | Liquid crystalline polyester resin for extrusion molding |
| JP4118425B2 (ja) | 1998-12-18 | 2008-07-16 | ポリプラスチックス株式会社 | コネクター用液晶性ポリマー組成物およびコネクター |
| US6379795B1 (en) | 1999-01-19 | 2002-04-30 | E. I. Du Pont De Nemours And Company | Injection moldable conductive aromatic thermoplastic liquid crystalline polymeric compositions |
| FI991006L (fi) | 1999-05-03 | 2000-11-04 | Optatech Oy | Uudet nestekiteiset polymeerit |
| JP4450902B2 (ja) | 1999-10-08 | 2010-04-14 | ポリプラスチックス株式会社 | 液晶性ポリマー組成物 |
| JP2001172479A (ja) | 1999-12-16 | 2001-06-26 | Sumitomo Chem Co Ltd | 液晶ポリエステル樹脂組成物およびその成形品 |
| CA2393259A1 (en) | 2000-01-13 | 2001-07-19 | E.I. Du Pont De Nemours And Company | Liquid crystalline polymer compositions containing small particle size fillers |
| US6114492A (en) | 2000-01-14 | 2000-09-05 | Ticona Llc | Process for producing liquid crystal polymer |
| JP4636644B2 (ja) * | 2000-01-17 | 2011-02-23 | 富士フイルム株式会社 | 電解質組成物、電気化学電池およびイオン性液晶モノマー |
| JP2001207054A (ja) | 2000-01-24 | 2001-07-31 | Polyplastics Co | 液晶性ポリマー成形品 |
| JP2001261946A (ja) | 2000-03-14 | 2001-09-26 | Polyplastics Co | 液晶性ポリマー組成物および成形方法 |
| US20020064701A1 (en) | 2000-09-11 | 2002-05-30 | Hand Doris I. | Conductive liquid crystalline polymer film and method of manufacture thereof |
| CN100406431C (zh) * | 2001-03-26 | 2008-07-30 | 日清纺织株式会社 | 离子液体、用于电存储设备的电解质盐、用于电存储设备的液体电解质、双电荷层电容器和二次电池 |
| JP2002294038A (ja) | 2001-03-28 | 2002-10-09 | Sumitomo Chem Co Ltd | 液晶ポリエステル樹脂組成物 |
| JP4033678B2 (ja) | 2001-03-30 | 2008-01-16 | 独立行政法人科学技術振興機構 | 液晶性イオン伝導体とその製造方法 |
| TWI242027B (en) | 2001-06-28 | 2005-10-21 | Sumitomo Chemical Co | Liquid crystal polyester resin mixture |
| US6514611B1 (en) | 2001-08-21 | 2003-02-04 | Ticona Llc | Anisotropic melt-forming polymers having a high degree of stretchability |
| JP3969171B2 (ja) | 2001-11-12 | 2007-09-05 | 住友化学株式会社 | 液晶性ポリエステルおよびその製造方法 |
| JPWO2003062286A1 (ja) | 2002-01-22 | 2005-05-19 | 独立行政法人科学技術振興機構 | 重合可能なイオン伝導性液晶性複合体と異方的イオン伝導性高分子液晶複合体並びにその製造方法 |
| JP4019731B2 (ja) | 2002-02-25 | 2007-12-12 | 住友化学株式会社 | コネクター用液晶性ポリエステル樹脂組成物 |
| JP2005532440A (ja) | 2002-07-05 | 2005-10-27 | デグサ アクチエンゲゼルシャフト | ポリマーとイオン性液体とからなるポリマー組成物 |
| JP3834528B2 (ja) | 2002-07-11 | 2006-10-18 | ポリマテック株式会社 | 熱伝導性高分子成形体の製造方法 |
| JP2004051852A (ja) | 2002-07-22 | 2004-02-19 | Polymatech Co Ltd | 熱伝導性高分子成形体及びその製造方法 |
| JP2005537379A (ja) | 2002-09-03 | 2005-12-08 | ソルヴェイ アドバンスド ポリマーズ リミテッド ライアビリティ カンパニー | 熱伝導性液晶ポリマー組成物及びそれから形成された製品 |
| TWI276660B (en) | 2002-12-18 | 2007-03-21 | Sumitomo Chemical Co | Aromatic liquid crystal polyester and film thereof |
| US20040135118A1 (en) | 2002-12-18 | 2004-07-15 | Waggoner Marion G. | Process for producing a liquid crystalline polymer |
| CA2523546A1 (en) | 2003-05-15 | 2004-12-02 | Gregory R. Alms | Fast crystallizing polyester compositions |
| KR101086123B1 (ko) | 2003-05-15 | 2011-11-25 | 이 아이 듀폰 디 네모아 앤드 캄파니 | 폴리에스테르 조성물 |
| JP2005015573A (ja) * | 2003-06-24 | 2005-01-20 | Mitsubishi Engineering Plastics Corp | 帯電防止性樹脂組成物 |
| US7547403B2 (en) | 2003-07-02 | 2009-06-16 | Polyplastics Co., Ltd. | Electroconductive resin composition |
| US8697817B2 (en) | 2003-09-04 | 2014-04-15 | Ticona Llc | Manufacturing process for liquid crystalline polymer |
| US7276284B2 (en) | 2003-12-18 | 2007-10-02 | Sgl-Carbon Ag | Carbon fiber reinforced coke from the delayed coker |
| US20050176835A1 (en) | 2004-01-12 | 2005-08-11 | Toshikazu Kobayashi | Thermally conductive thermoplastic resin compositions |
| US20050191877A1 (en) | 2004-03-01 | 2005-09-01 | Peter Huang | Electrical connector |
| DE602005014218D1 (de) | 2004-03-10 | 2009-06-10 | Panasonic Elec Works Co Ltd | Metallbeschichteter harzformkörper und herstellungsverfahren dafür |
| JP4016010B2 (ja) | 2004-03-26 | 2007-12-05 | 株式会社東芝 | リアルタイムスケジューリング可能性判定方法およびリアルタイムシステム |
| WO2005099984A1 (ja) | 2004-04-15 | 2005-10-27 | Polyplastics Co., Ltd. | 繊維状充填剤の長さが制御された樹脂組成物ペレットの製造方法 |
| JP4871495B2 (ja) * | 2004-06-11 | 2012-02-08 | 三光化学工業株式会社 | 制電性組成物、その製造方法、及びそれを用いた成形品 |
| JP4664626B2 (ja) | 2004-07-05 | 2011-04-06 | ポリマテック株式会社 | イオン伝導性高分子電解質膜及びその製造方法 |
| JP4463637B2 (ja) | 2004-07-30 | 2010-05-19 | ポリプラスチックス株式会社 | 液晶性ポリエステル樹脂組成物 |
| JP2006045298A (ja) | 2004-08-03 | 2006-02-16 | Ntn Corp | 液晶ポリエステル樹脂組成物 |
| JP4763987B2 (ja) * | 2004-08-27 | 2011-08-31 | 帝人化成株式会社 | ポリカーボネート樹脂組成物 |
| JP4665475B2 (ja) | 2004-09-30 | 2011-04-06 | 住友化学株式会社 | 芳香族液晶ポリエステルフィルム |
| JP4498900B2 (ja) | 2004-11-29 | 2010-07-07 | ポリプラスチックス株式会社 | 信号読取装置用樹脂成形部品及びその成形方法 |
| CN1828354A (zh) | 2005-03-04 | 2006-09-06 | 普立尔科技股份有限公司 | 照相机模块及其制备方法 |
| US7438832B2 (en) | 2005-03-29 | 2008-10-21 | Eastman Kodak Company | Ionic liquid and electronically conductive polymer mixtures |
| KR100702859B1 (ko) | 2005-05-27 | 2007-04-03 | 부산대학교 산학협력단 | 액정 물질을 포함하는 고체 전해질 및 이를 이용한염료감응형 태양전지 소자 |
| US7825176B2 (en) | 2005-08-31 | 2010-11-02 | Sabic Innovative Plastics Ip B.V. | High flow polyester composition |
| US20070057236A1 (en) | 2005-09-12 | 2007-03-15 | Sumitomo Chemical Company, Limited | Conductive resin composition and the use thereof |
| DE102006048637A1 (de) | 2005-10-13 | 2007-04-19 | Polyplastics Co. Ltd. | Flüssigkristalline Harzzusammensetzung zum Blasformen |
| KR20080098031A (ko) | 2006-02-13 | 2008-11-06 | 폴리플라스틱스 가부시키가이샤 | 열가소성 수지 조성물 및 그 액정 디스플레이 부품 또는 정보 기록 매체 부품 |
| US7931824B2 (en) * | 2006-07-03 | 2011-04-26 | The Regents Of The University Of Colorado | Surfactants and polymerizable surfactants based on room-temperature ionic liquids that form lyotropic liquid crystal phases with water and room-temperature ionic liquids |
| WO2008005906A2 (en) * | 2006-07-03 | 2008-01-10 | Matheson Tri-Gas, Inc. | Fluid storage and purification method and system using ionic liquid in particular di-imidazolium cation |
| JP2008075063A (ja) | 2006-08-22 | 2008-04-03 | Sumitomo Chemical Co Ltd | 液晶性ポリマー成形体 |
| TWI472574B (zh) | 2006-08-24 | 2015-02-11 | Polyplastics Co | 非對稱電子零件 |
| JP5332188B2 (ja) | 2007-02-26 | 2013-11-06 | 住友化学株式会社 | 樹脂成形体及びその製造方法 |
| JP5384023B2 (ja) | 2007-04-23 | 2014-01-08 | 上野製薬株式会社 | 液晶ポリマー組成物およびそれからなる成形品 |
| US8029694B2 (en) | 2007-04-24 | 2011-10-04 | E.I. Du Pont De Nemours And Company | Thermally conductive and electrically resistive liquid crystalline polymer composition |
| JP2009030015A (ja) | 2007-06-27 | 2009-02-12 | Sumitomo Chemical Co Ltd | 液晶性ポリエステル組成物 |
| KR101087695B1 (ko) | 2007-07-03 | 2011-11-30 | 주식회사 옵토메카 | 이종재료 일체형 렌즈 유닛 및 이를 구비하는 카메라 모듈 |
| ES2358132T3 (es) | 2007-08-24 | 2011-05-05 | Ems-Patent Ag | Masas moldeadas de poliamida a alta temperatura reforzadas con fibras de vidrio planas. |
| US8432484B2 (en) | 2007-10-31 | 2013-04-30 | STMicroelectronics (R&D) Ltd. | Camera modules |
| JP2009155623A (ja) | 2007-12-03 | 2009-07-16 | Sumitomo Chemical Co Ltd | 液晶ポリエステル樹脂組成物及びその成形体 |
| JP2009231269A (ja) | 2008-02-25 | 2009-10-08 | Sumitomo Chemical Co Ltd | 反射板及び発光装置 |
| CN101981123B (zh) * | 2008-03-28 | 2012-11-21 | 吉坤日矿日石能源株式会社 | 照相机模块用液晶聚酯树脂组合物 |
| JP5325442B2 (ja) * | 2008-03-28 | 2013-10-23 | Ｊｘ日鉱日石エネルギー株式会社 | カメラモジュール用液晶ポリエステル樹脂組成物 |
| JP5165492B2 (ja) | 2008-05-23 | 2013-03-21 | ポリプラスチックス株式会社 | 平面状コネクター |
| US20100012354A1 (en) | 2008-07-14 | 2010-01-21 | Logan Brook Hedin | Thermally conductive polymer based printed circuit board |
| EP2147776A1 (de) | 2008-07-23 | 2010-01-27 | SGL Carbon SE | Verfahren zur Herstellung eines Fasergelege-verstärkten Verbundwerkstoffs, sowie Fasergelege-verstärkte Verbundwerkstoffe und deren Verwendung |
| KR101639439B1 (ko) | 2008-12-25 | 2016-07-13 | 스미또모 가가꾸 가부시키가이샤 | 액정성 폴리에스테르 수지 조성물 및 이것을 사용한 커넥터 |
| JP5503915B2 (ja) | 2009-07-30 | 2014-05-28 | 住友化学株式会社 | 液晶ポリエステル組成物およびこれを用いた電子回路基板 |
| JP5486889B2 (ja) | 2009-09-28 | 2014-05-07 | Ｊｘ日鉱日石エネルギー株式会社 | 液晶ポリエステル樹脂組成物 |
| JP2011094116A (ja) * | 2009-09-29 | 2011-05-12 | Sumitomo Chemical Co Ltd | 液晶ポリエステル樹脂組成物、成形体および光ピックアップレンズホルダー |
| KR101708927B1 (ko) | 2009-10-09 | 2017-02-21 | 심천 워트 어드밴스드 머티리얼즈 주식회사 | 내열성이 향상된 전방향족 액정 폴리에스테르 수지 컴파운드 및 그의 제조방법 |
| KR101783477B1 (ko) | 2009-10-21 | 2017-09-29 | 심천 워트 어드밴스드 머티리얼즈 주식회사 | 전방향족 액정 폴리에스테르 수지 컴파운드, 상기 수지 컴파운드의 제조방법, 광픽업용 부품, 및 상기 부품의 제조방법 |
| TW201132747A (en) | 2009-11-16 | 2011-10-01 | Sumitomo Chemical Co | Liquid crystalline polyester composition for connector and connector using the same |
| KR101004428B1 (ko) | 2009-12-30 | 2010-12-28 | 주식회사 대림코퍼레이션 | 대전방지특성 또는 전기전도특성을 가지는 전방향족 폴리이미드 분말의 제조방법 |
| JP2011157422A (ja) | 2010-01-29 | 2011-08-18 | Sumitomo Chemical Co Ltd | 液晶ポリエステル組成物、その製造方法及びコネクター |
| JP5504923B2 (ja) | 2010-01-29 | 2014-05-28 | 住友化学株式会社 | 液晶ポリエステル組成物の製造方法及びコネクター |
| SG183459A1 (en) | 2010-02-25 | 2012-09-27 | Ticona Llc | Thermally conductive and dimensionally stable liquid crystalline polymer composition |
| KR101792987B1 (ko) | 2010-03-16 | 2017-11-02 | 제이엑스티지 에네루기 가부시키가이샤 | 전방향족 서모트로픽 액정 폴리에스테르 수지 조성물, 성형체 및 ｌｅｄ 리플렉터 |
| JP2011202062A (ja) * | 2010-03-26 | 2011-10-13 | Sumitomo Chemical Co Ltd | 摺動用熱可塑性樹脂組成物、摺動用熱可塑性樹脂組成物の製造方法および摺動部品 |
| JP2012046621A (ja) * | 2010-08-26 | 2012-03-08 | Panasonic Electric Works Co Ltd | 成形品及びコネクタ |
| JP5695389B2 (ja) | 2010-10-15 | 2015-04-01 | Ｊｘ日鉱日石エネルギー株式会社 | 液晶ポリエステル樹脂組成物及びカメラモジュール部品 |
| KR101711214B1 (ko) | 2010-11-12 | 2017-02-28 | 심천 워트 어드밴스드 머티리얼즈 주식회사 | 반사체 및 이를 구비하는 발광장치 |
| KR20120052647A (ko) | 2010-11-16 | 2012-05-24 | 삼성정밀화학 주식회사 | 유동성이 향상된 전방향족 액정 폴리에스테르 수지 컴파운드 |
| KR101228705B1 (ko) | 2010-12-27 | 2013-02-01 | 도레이 카부시키가이샤 | 전방향족 액정 폴리에스테르 및 그 제조 방법 |
| WO2012090411A1 (ja) | 2010-12-28 | 2012-07-05 | 東レ株式会社 | 液晶性ポリエステル樹脂組成物及びその製造方法とそれからなる成形品 |
| WO2012090410A1 (ja) | 2010-12-28 | 2012-07-05 | 東レ株式会社 | 液晶性ポリエステル樹脂組成物及びその製造方法とそれからなる成形品 |
| JP5723618B2 (ja) | 2011-02-04 | 2015-05-27 | 日東電工株式会社 | 粘着シートおよび表面保護フィルム |
| US9045621B2 (en) | 2011-02-28 | 2015-06-02 | Toray Industries, Inc. | Liquid crystalline polyester composition and metal composite molded product using the same |
| TWI586750B (zh) * | 2011-02-28 | 2017-06-11 | 住友化學股份有限公司 | 液晶聚酯組成物及其製造方法 |
| KR20120114048A (ko) | 2011-04-06 | 2012-10-16 | 삼성정밀화학 주식회사 | 열전도성 고분자 복합소재 및 이를 포함하는 물품 |
| JP5730704B2 (ja) | 2011-07-27 | 2015-06-10 | 上野製薬株式会社 | 液晶ポリマー組成物 |
| WO2013032970A1 (en) | 2011-08-29 | 2013-03-07 | Ticona Llc | Liquid crystalline polymer composition containing a fibrous filler |
| TWI554594B (zh) | 2011-08-29 | 2016-10-21 | 堤康那責任有限公司 | 高流量液晶聚合物組合物 |
| US9045685B2 (en) | 2011-08-29 | 2015-06-02 | Ticona Llc | Cast molded parts formed from a liquid crystalline polymer |
| TW201319223A (zh) | 2011-08-29 | 2013-05-16 | Ticona Llc | 高流量液晶聚合物組合物 |
| WO2013074467A1 (en) | 2011-11-15 | 2013-05-23 | Ticona Llc | Low naphthenic liquid crystalline polymer composition for use in molded parts of a small dimensional tolerance |
| US20130123420A1 (en) | 2011-11-15 | 2013-05-16 | Ticona Llc | Liquid Crystalline Polymer Composition for High Voltage Electronic Components |
| CN103930464B (zh) | 2011-11-15 | 2016-02-10 | 提克纳有限责任公司 | 紧凑型相机模块 |
| WO2013074477A1 (en) | 2011-11-15 | 2013-05-23 | Ticona Llc | Naphthenic-rich liquid crystalline polymer composition with improved flammability performance |
| US8932483B2 (en) | 2011-11-15 | 2015-01-13 | Ticona Llc | Low naphthenic liquid crystalline polymer composition |
| KR102093832B1 (ko) | 2012-02-08 | 2020-03-26 | 메르크 파텐트 게엠베하 | 전도성 첨가제를 포함하는 반응성 메소겐 제제 |
| US9284435B2 (en) * | 2012-10-16 | 2016-03-15 | Ticona Llc | Antistatic liquid crystalline polymer composition |
| WO2014088700A1 (en) | 2012-12-05 | 2014-06-12 | Ticona Llc | Conductive liquid crystalline polymer composition |
| CN111732821A (zh) * | 2013-03-13 | 2020-10-02 | 提克纳有限责任公司 | 抗静电液晶聚合物组合物 |
-
2013
- 2013-10-14 US US14/052,789 patent/US9284435B2/en active Active
- 2013-10-14 CN CN201380053722.7A patent/CN104736672B/zh active Active
- 2013-10-14 JP JP2015537754A patent/JP6462576B2/ja active Active
- 2013-10-14 KR KR1020157009445A patent/KR102246137B1/ko active Active
- 2013-10-14 WO PCT/US2013/064760 patent/WO2014062536A1/en not_active Ceased
- 2013-10-14 TW TW102137022A patent/TWI646135B/zh active
-
2016
- 2016-03-10 US US15/065,986 patent/US9988519B2/en active Active
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI230176B (en) * | 1999-10-06 | 2005-04-01 | 3M Innovative Properties Co | Antistatic composition |
| TW201235406A (en) * | 2010-11-30 | 2012-09-01 | Sumitomo Chemical Co | Liquid crystalline polyester composition |
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| TW201431932A (zh) | 2014-08-16 |
| KR102246137B1 (ko) | 2021-04-28 |
| WO2014062536A1 (en) | 2014-04-24 |
| US9988519B2 (en) | 2018-06-05 |
| JP2015532353A (ja) | 2015-11-09 |
| US20160185940A1 (en) | 2016-06-30 |
| KR20150073171A (ko) | 2015-06-30 |
| US20140105590A1 (en) | 2014-04-17 |
| JP6462576B2 (ja) | 2019-01-30 |
| CN104736672A (zh) | 2015-06-24 |
| CN104736672B (zh) | 2017-10-24 |
| US9284435B2 (en) | 2016-03-15 |
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