JPH0216929B2 - - Google Patents

Info

Publication number: JPH0216929B2
Authority: JP; Japan
Prior art keywords: polyester; fibers; strength; melt; units
Prior art date: 1983-08-31
Legal status (The legal status 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 status listed.): Expired

Application number

JP15998383A

Other languages

English (en)

Japanese (ja)

Other versions

JPS6051718A (ja

Inventor

Hideo Kasatani

Takashi Fujiwara

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Asahi Chemical Industry Co Ltd

Original Assignee

Asahi Chemical Industry Co Ltd

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.)

1983-08-31

Filing date

1983-08-31

Publication date

1990-04-18

1983-08-31 Application filed by Asahi Chemical Industry Co Ltd filed Critical Asahi Chemical Industry Co Ltd

1983-08-31 Priority to JP15998383A priority Critical patent/JPS6051718A/ja

1984-08-28 Priority to US06/645,413 priority patent/US4529565A/en

1985-03-23 Publication of JPS6051718A publication Critical patent/JPS6051718A/ja

1990-04-18 Publication of JPH0216929B2 publication Critical patent/JPH0216929B2/ja

Status Granted legal-status Critical Current

Links

229920000728 polyester Polymers 0.000 claims description 69
125000003118 aryl group Chemical group 0.000 claims description 17
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 6
125000001309 chloro group Chemical group Cl* 0.000 claims description 5
QPFMBZIOSGYJDE-UHFFFAOYSA-N 1,1,2,2-tetrachloroethane Chemical compound ClC(Cl)C(Cl)Cl QPFMBZIOSGYJDE-UHFFFAOYSA-N 0.000 claims description 4
239000012046 mixed solvent Substances 0.000 claims description 3
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 2
229910052801 chlorine Inorganic materials 0.000 claims description 2
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
WXNZTHHGJRFXKQ-UHFFFAOYSA-N 4-chlorophenol Chemical compound OC1=CC=C(Cl)C=C1 WXNZTHHGJRFXKQ-UHFFFAOYSA-N 0.000 claims 1
239000000835 fiber Substances 0.000 description 32
238000010438 heat treatment Methods 0.000 description 22
KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 14
238000002844 melting Methods 0.000 description 13
230000008018 melting Effects 0.000 description 13
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 11
230000000704 physical effect Effects 0.000 description 11
-1 polyethylene terephthalate Polymers 0.000 description 11
238000006116 polymerization reaction Methods 0.000 description 11
238000000034 method Methods 0.000 description 8
QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 7
238000000465 moulding Methods 0.000 description 7
FJKROLUGYXJWQN-UHFFFAOYSA-N 4-hydroxybenzoic acid Chemical compound OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 6
238000006243 chemical reaction Methods 0.000 description 6
239000012783 reinforcing fiber Substances 0.000 description 6
238000009987 spinning Methods 0.000 description 6
NTKLFSYUWYPMCJ-UHFFFAOYSA-N 2-phenoxybenzene-1,4-diol Chemical compound OC1=CC=C(O)C(OC=2C=CC=CC=2)=C1 NTKLFSYUWYPMCJ-UHFFFAOYSA-N 0.000 description 5
229910052757 nitrogen Inorganic materials 0.000 description 5
238000002074 melt spinning Methods 0.000 description 4
XCZKKZXWDBOGPA-UHFFFAOYSA-N 2-phenylbenzene-1,4-diol Chemical compound OC1=CC=C(O)C(C=2C=CC=CC=2)=C1 XCZKKZXWDBOGPA-UHFFFAOYSA-N 0.000 description 3
GDBUZIKSJGRBJP-UHFFFAOYSA-N 4-acetoxy benzoic acid Chemical compound CC(=O)OC1=CC=C(C(O)=O)C=C1 GDBUZIKSJGRBJP-UHFFFAOYSA-N 0.000 description 3
229940090248 4-hydroxybenzoic acid Drugs 0.000 description 3
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
PRCCLKLILIHZMR-UHFFFAOYSA-N C(C)(=O)O.C(C)(=O)O.O(C1=CC=CC=C1)C1=C(O)C=CC(=C1)O Chemical compound C(C)(=O)O.C(C)(=O)O.O(C1=CC=CC=C1)C1=C(O)C=CC(=C1)O PRCCLKLILIHZMR-UHFFFAOYSA-N 0.000 description 3
238000004455 differential thermal analysis Methods 0.000 description 3
150000002009 diols Chemical class 0.000 description 3
230000000694 effects Effects 0.000 description 3
239000000203 mixture Substances 0.000 description 3
238000006068 polycondensation reaction Methods 0.000 description 3
229920000642 polymer Polymers 0.000 description 3
239000011347 resin Substances 0.000 description 3
229920005989 resin Polymers 0.000 description 3
238000003756 stirring Methods 0.000 description 3
AKOGNYJNGMLDOA-UHFFFAOYSA-N (4-acetyloxyphenyl) acetate Chemical compound CC(=O)OC1=CC=C(OC(C)=O)C=C1 AKOGNYJNGMLDOA-UHFFFAOYSA-N 0.000 description 2
XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
238000000862 absorption spectrum Methods 0.000 description 2
239000002253 acid Substances 0.000 description 2
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
230000000052 comparative effect Effects 0.000 description 2
230000006866 deterioration Effects 0.000 description 2
235000014113 dietary fatty acids Nutrition 0.000 description 2
WOZVHXUHUFLZGK-UHFFFAOYSA-N dimethyl terephthalate Chemical compound COC(=O)C1=CC=C(C(=O)OC)C=C1 WOZVHXUHUFLZGK-UHFFFAOYSA-N 0.000 description 2
HPGJOUYGWKFYQW-UHFFFAOYSA-N diphenyl benzene-1,4-dicarboxylate Chemical compound C=1C=C(C(=O)OC=2C=CC=CC=2)C=CC=1C(=O)OC1=CC=CC=C1 HPGJOUYGWKFYQW-UHFFFAOYSA-N 0.000 description 2
238000000921 elemental analysis Methods 0.000 description 2
239000000194 fatty acid Substances 0.000 description 2
229930195729 fatty acid Natural products 0.000 description 2
239000004973 liquid crystal related substance Substances 0.000 description 2
239000000463 material Substances 0.000 description 2
239000000155 melt Substances 0.000 description 2
238000002156 mixing Methods 0.000 description 2
239000000178 monomer Substances 0.000 description 2
230000003287 optical effect Effects 0.000 description 2
239000001301 oxygen Substances 0.000 description 2
229910052760 oxygen Inorganic materials 0.000 description 2
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
IOLCXVTUBQKXJR-UHFFFAOYSA-M potassium bromide Chemical compound [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 description 2
238000011160 research Methods 0.000 description 2
239000007790 solid phase Substances 0.000 description 2
238000002411 thermogravimetry Methods 0.000 description 2
CNHDIAIOKMXOLK-UHFFFAOYSA-N toluquinol Chemical compound CC1=CC(O)=CC=C1O CNHDIAIOKMXOLK-UHFFFAOYSA-N 0.000 description 2
238000005292 vacuum distillation Methods 0.000 description 2
MGAXYKDBRBNWKT-UHFFFAOYSA-N (5-oxooxolan-2-yl)methyl 4-methylbenzenesulfonate Chemical compound C1=CC(C)=CC=C1S(=O)(=O)OCC1OC(=O)CC1 MGAXYKDBRBNWKT-UHFFFAOYSA-N 0.000 description 1
150000005208 1,4-dihydroxybenzenes Chemical class 0.000 description 1
SOPOGHYPTKLNBE-UHFFFAOYSA-N 1,4-dimethoxy-2-phenoxybenzene Chemical compound COC1=CC=C(OC)C(OC=2C=CC=CC=2)=C1 SOPOGHYPTKLNBE-UHFFFAOYSA-N 0.000 description 1
DWCGNRKFLRLWCJ-UHFFFAOYSA-N 2-bromo-1,4-dimethoxybenzene Chemical compound COC1=CC=C(OC)C(Br)=C1 DWCGNRKFLRLWCJ-UHFFFAOYSA-N 0.000 description 1
SWZVJOLLQTWFCW-UHFFFAOYSA-N 2-chlorobenzene-1,3-diol Chemical group OC1=CC=CC(O)=C1Cl SWZVJOLLQTWFCW-UHFFFAOYSA-N 0.000 description 1
ISPYQTSUDJAMAB-UHFFFAOYSA-N 2-chlorophenol Chemical compound OC1=CC=CC=C1Cl ISPYQTSUDJAMAB-UHFFFAOYSA-N 0.000 description 1
ZTMADXFOCUXMJE-UHFFFAOYSA-N 2-methylbenzene-1,3-diol Chemical group CC1=C(O)C=CC=C1O ZTMADXFOCUXMJE-UHFFFAOYSA-N 0.000 description 1
HPVTTYNAENJWQG-UHFFFAOYSA-N 2-phenoxybenzene-1,3-diol Chemical group OC1=CC=CC(O)=C1OC1=CC=CC=C1 HPVTTYNAENJWQG-UHFFFAOYSA-N 0.000 description 1
IJFXRHURBJZNAO-UHFFFAOYSA-N 3-hydroxybenzoic acid Chemical group OC(=O)C1=CC=CC(O)=C1 IJFXRHURBJZNAO-UHFFFAOYSA-N 0.000 description 1
125000005274 4-hydroxybenzoic acid group Chemical group 0.000 description 1
BSYNRYMUTXBXSQ-UHFFFAOYSA-N Aspirin Chemical compound CC(=O)OC1=CC=CC=C1C(O)=O BSYNRYMUTXBXSQ-UHFFFAOYSA-N 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
229920000049 Carbon (fiber) Polymers 0.000 description 1
102100038736 Histone H3.3C Human genes 0.000 description 1
101001031505 Homo sapiens Histone H3.3C Proteins 0.000 description 1
229920002302 Nylon 6,6 Polymers 0.000 description 1
239000004952 Polyamide Substances 0.000 description 1
229910000831 Steel Inorganic materials 0.000 description 1
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
BSPZSNZSYCFYBF-UHFFFAOYSA-N acetic acid;2-phenylbenzene-1,4-diol Chemical compound CC(O)=O.CC(O)=O.OC1=CC=C(O)C(C=2C=CC=CC=2)=C1 BSPZSNZSYCFYBF-UHFFFAOYSA-N 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
238000004458 analytical method Methods 0.000 description 1
229910052787 antimony Inorganic materials 0.000 description 1
WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 1
239000004760 aramid Substances 0.000 description 1
229920006231 aramid fiber Polymers 0.000 description 1
229910052786 argon Inorganic materials 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical group C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 1
125000004432 carbon atom Chemical group C* 0.000 description 1
239000004917 carbon fiber Substances 0.000 description 1
150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
239000003054 catalyst Substances 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
AJPXTSMULZANCB-UHFFFAOYSA-N chlorohydroquinone Chemical compound OC1=CC=C(O)C(Cl)=C1 AJPXTSMULZANCB-UHFFFAOYSA-N 0.000 description 1
239000006059 cover glass Substances 0.000 description 1
230000006378 damage Effects 0.000 description 1
238000000354 decomposition reaction Methods 0.000 description 1
238000010586 diagram Methods 0.000 description 1
238000000113 differential scanning calorimetry Methods 0.000 description 1
229910001873 dinitrogen Inorganic materials 0.000 description 1
238000001035 drying Methods 0.000 description 1
238000005516 engineering process Methods 0.000 description 1
238000001125 extrusion Methods 0.000 description 1
230000002349 favourable effect Effects 0.000 description 1
150000002291 germanium compounds Chemical class 0.000 description 1
239000011521 glass Substances 0.000 description 1
239000010439 graphite Substances 0.000 description 1
229910002804 graphite Inorganic materials 0.000 description 1
239000012761 high-performance material Substances 0.000 description 1
229920001519 homopolymer Polymers 0.000 description 1
230000003301 hydrolyzing effect Effects 0.000 description 1
NWVVVBRKAWDGAB-UHFFFAOYSA-N hydroquinone methyl ether Natural products COC1=CC=C(O)C=C1 NWVVVBRKAWDGAB-UHFFFAOYSA-N 0.000 description 1
238000010348 incorporation Methods 0.000 description 1
239000012770 industrial material Substances 0.000 description 1
239000011261 inert gas Substances 0.000 description 1
239000012784 inorganic fiber Substances 0.000 description 1
238000009413 insulation Methods 0.000 description 1
QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical group OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
239000006224 matting agent Substances 0.000 description 1
238000000691 measurement method Methods 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
229920000620 organic polymer Polymers 0.000 description 1
230000001590 oxidative effect Effects 0.000 description 1
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
GJLNWLVPAHNBQN-UHFFFAOYSA-N phenyl 4-hydroxybenzoate Chemical compound C1=CC(O)=CC=C1C(=O)OC1=CC=CC=C1 GJLNWLVPAHNBQN-UHFFFAOYSA-N 0.000 description 1
ZQBAKBUEJOMQEX-UHFFFAOYSA-N phenyl salicylate Chemical compound OC1=CC=CC=C1C(=O)OC1=CC=CC=C1 ZQBAKBUEJOMQEX-UHFFFAOYSA-N 0.000 description 1
229910052698 phosphorus Inorganic materials 0.000 description 1
239000011574 phosphorus Substances 0.000 description 1
239000004033 plastic Substances 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
229920002647 polyamide Polymers 0.000 description 1
229920000139 polyethylene terephthalate Polymers 0.000 description 1
239000005020 polyethylene terephthalate Substances 0.000 description 1
239000002861 polymer material Substances 0.000 description 1
239000000843 powder Substances 0.000 description 1
238000012545 processing Methods 0.000 description 1
230000009257 reactivity Effects 0.000 description 1
GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical group OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 1
239000002904 solvent Substances 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
239000010959 steel Substances 0.000 description 1
238000006467 substitution reaction Methods 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
238000002076 thermal analysis method Methods 0.000 description 1
OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
238000004804 winding Methods 0.000 description 1

Landscapes

Polyesters Or Polycarbonates (AREA)

JP15998383A 1983-08-31 1983-08-31 芳香族ポリエステル Granted JPS6051718A (ja)

Priority Applications (2)

Application Number	Priority Date	Filing Date	Title
JP15998383A JPS6051718A (ja)	1983-08-31	1983-08-31	芳香族ポリエステル
US06/645,413 US4529565A (en)	1983-08-31	1984-08-28	Polyester of substituted or unsubstituted phenoxyhydroquinone

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP15998383A JPS6051718A (ja)	1983-08-31	1983-08-31	芳香族ポリエステル

Publications (2)

Publication Number	Publication Date
JPS6051718A JPS6051718A (ja)	1985-03-23
JPH0216929B2 true JPH0216929B2 (ko)	1990-04-18

Family

ID=15705434

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP15998383A Granted JPS6051718A (ja)	1983-08-31	1983-08-31	芳香族ポリエステル

Country Status (1)

Country	Link
JP (1)	JPS6051718A (ko)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS6321922U (ko) *	1986-07-28	1988-02-13
JP2007151337A (ja) *	2005-11-29	2007-06-14	Chugoku Electric Power Co Inc:The	ケーブル保持具
CN102675578B (zh) *	2012-05-07	2013-11-13	上海交通大学	芳基聚酯聚氨酯树脂

1983
- 1983-08-31 JP JP15998383A patent/JPS6051718A/ja active Granted

Also Published As

Publication number	Publication date
JPS6051718A (ja)	1985-03-23

Publication	Publication Date	Title
JPS633891B2 (ko)	1988-01-26
JPH0149804B2 (ko)	1989-10-26
JP2001200034A (ja)	2001-07-24	伸縮自在なポリマーを製造するための組成物および方法ならびにそれらによって製造される造形物品
US4529565A (en)	1985-07-16	Polyester of substituted or unsubstituted phenoxyhydroquinone
JPS62292832A (ja)	1987-12-19	耐熱性芳香族ポリエステル
JPS63182332A (ja)	1988-07-27	液晶性ポリエステル
JP3001732B2 (ja)	2000-01-24	共重合ポリエステルおよびそれから得られる繊維
JPS6326129B2 (ko)	1988-05-28
JPH0216929B2 (ko)	1990-04-18
JPS5891818A (ja)	1983-05-31	イミド基を含有したポリエステルからなる繊維またはフイルムおよびそれらの製法
JPS60108421A (ja)	1985-06-13	新規なポリエステル
JP3056604B2 (ja)	2000-06-26	新規ポリエステルおよびその繊維
JPS60130619A (ja)	1985-07-12	芳香族性ポリエステル
JPS63101416A (ja)	1988-05-06	全芳香族ポリエステル重合体
JPS60199028A (ja)	1985-10-08	新規なポリエステル
JPS60130618A (ja)	1985-07-12	全芳香族ポリエステル
JP2544731B2 (ja)	1996-10-16	全芳香族ポリエステル
JPS61157527A (ja)	1986-07-17	異方性溶融相を形成しうる全芳香族ポリエステル
JPS6258378B2 (ko)	1987-12-05
JPS60203631A (ja)	1985-10-15	ポリエステル
JPS62265325A (ja)	1987-11-18	新規な芳香族ポリエステル
JP3056601B2 (ja)	2000-06-26	共重合ポリエステルおよびその繊維
JP3056603B2 (ja)	2000-06-26	新規ポリエステル及びそれからなる繊維
KR960007607B1 (ko)	1996-06-07	폴리에스테르 공중합체의 제조방법
JPS6335618A (ja)	1988-02-16	新規な全芳香族ポリエステル