JPS6347748B2 - - Google Patents

Info

Publication number: JPS6347748B2
Authority: JP; Japan
Prior art keywords: weight; parts; acid; aromatic polyester; copolymer
Prior art date: 1978-06-15
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

JP53072402A

Other languages

English (en)

Japanese (ja)

Other versions

JPS54162750A (en

Inventor

Kiichi Yonetani

Hidesada Okasaka

Masanobu Morikawa

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.)

Toray Industries Inc

Original Assignee

Toray Industries Inc

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.)

1978-06-15

Filing date

1978-06-15

Publication date

1988-09-26

1978-06-15 Application filed by Toray Industries Inc filed Critical Toray Industries Inc

1978-06-15 Priority to JP7240278A priority Critical patent/JPS54162750A/ja

1979-12-24 Publication of JPS54162750A publication Critical patent/JPS54162750A/ja

1988-09-26 Publication of JPS6347748B2 publication Critical patent/JPS6347748B2/ja

Status Granted legal-status Critical Current

Links

125000003118 aryl group Chemical group 0.000 claims description 25
229920000728 polyester Polymers 0.000 claims description 24
229920001577 copolymer Polymers 0.000 claims description 22
125000003700 epoxy group Chemical group 0.000 claims description 18
239000000203 mixture Substances 0.000 claims description 14
150000002903 organophosphorus compounds Chemical class 0.000 claims description 13
239000000178 monomer Substances 0.000 claims description 11
125000004432 carbon atom Chemical group C* 0.000 claims description 7
OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 6
PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 claims description 3
229920000642 polymer Polymers 0.000 description 18
-1 fatty acid diol Chemical class 0.000 description 16
238000002844 melting Methods 0.000 description 9
230000008018 melting Effects 0.000 description 9
238000000034 method Methods 0.000 description 9
239000000155 melt Substances 0.000 description 8
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 7
239000005977 Ethylene Substances 0.000 description 7
230000000052 comparative effect Effects 0.000 description 6
KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 4
238000000071 blow moulding Methods 0.000 description 4
WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 4
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 3
239000002253 acid Substances 0.000 description 3
150000002148 esters Chemical class 0.000 description 3
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
238000000465 moulding Methods 0.000 description 3
VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 2
KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 2
239000004593 Epoxy Substances 0.000 description 2
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-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
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
239000006085 branching agent Substances 0.000 description 2
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
229910002091 carbon monoxide Inorganic materials 0.000 description 2
150000001875 compounds Chemical class 0.000 description 2
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 2
USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
238000001125 extrusion Methods 0.000 description 2
230000001771 impaired effect Effects 0.000 description 2
238000001746 injection moulding Methods 0.000 description 2
239000012948 isocyanate Substances 0.000 description 2
150000002513 isocyanates Chemical class 0.000 description 2
QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 2
RPQRDASANLAFCM-UHFFFAOYSA-N oxiran-2-ylmethyl prop-2-enoate Chemical group C=CC(=O)OCC1CO1 RPQRDASANLAFCM-UHFFFAOYSA-N 0.000 description 2
125000004437 phosphorous atom Chemical group 0.000 description 2
229910052698 phosphorus Inorganic materials 0.000 description 2
XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
229920001707 polybutylene terephthalate Polymers 0.000 description 2
238000006116 polymerization reaction Methods 0.000 description 2
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
239000000126 substance Substances 0.000 description 2
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 2
PXGZQGDTEZPERC-UHFFFAOYSA-N 1,4-cyclohexanedicarboxylic acid Chemical compound OC(=O)C1CCC(C(O)=O)CC1 PXGZQGDTEZPERC-UHFFFAOYSA-N 0.000 description 1
AFFLGGQVNFXPEV-UHFFFAOYSA-N 1-decene Chemical compound CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 1
ISPYQTSUDJAMAB-UHFFFAOYSA-N 2-chlorophenol Chemical compound OC1=CC=CC=C1Cl ISPYQTSUDJAMAB-UHFFFAOYSA-N 0.000 description 1
NMSZFQAFWHFSPE-UHFFFAOYSA-N 3-(oxiran-2-ylmethoxycarbonyl)but-3-enoic acid Chemical compound OC(=O)CC(=C)C(=O)OCC1CO1 NMSZFQAFWHFSPE-UHFFFAOYSA-N 0.000 description 1
XAYDWGMOPRHLEP-UHFFFAOYSA-N 6-ethenyl-7-oxabicyclo[4.1.0]heptane Chemical compound C1CCCC2OC21C=C XAYDWGMOPRHLEP-UHFFFAOYSA-N 0.000 description 1
HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical class NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
GXBYFVGCMPJVJX-UHFFFAOYSA-N Epoxybutene Chemical compound C=CC1CO1 GXBYFVGCMPJVJX-UHFFFAOYSA-N 0.000 description 1
QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 1
239000006096 absorbing agent Substances 0.000 description 1
239000000654 additive Substances 0.000 description 1
235000011037 adipic acid Nutrition 0.000 description 1
239000001361 adipic acid Substances 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
125000002723 alicyclic group Chemical group 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
150000001336 alkenes Chemical class 0.000 description 1
125000003545 alkoxy group Chemical group 0.000 description 1
125000004414 alkyl thio group Chemical group 0.000 description 1
125000003277 amino group Chemical group 0.000 description 1
FNGGVJIEWDRLFV-UHFFFAOYSA-N anthracene-1,2-dicarboxylic acid Chemical compound C1=CC=CC2=CC3=C(C(O)=O)C(C(=O)O)=CC=C3C=C21 FNGGVJIEWDRLFV-UHFFFAOYSA-N 0.000 description 1
239000003963 antioxidant agent Substances 0.000 description 1
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
229910052794 bromium Inorganic materials 0.000 description 1
150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
239000003153 chemical reaction reagent Substances 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
239000000460 chlorine Substances 0.000 description 1
239000003086 colorant Substances 0.000 description 1
238000006482 condensation reaction Methods 0.000 description 1
238000007334 copolymerization reaction Methods 0.000 description 1
PDXRQENMIVHKPI-UHFFFAOYSA-N cyclohexane-1,1-diol Chemical compound OC1(O)CCCCC1 PDXRQENMIVHKPI-UHFFFAOYSA-N 0.000 description 1
XBZSBBLNHFMTEB-UHFFFAOYSA-N cyclohexane-1,3-dicarboxylic acid Chemical compound OC(=O)C1CCCC(C(O)=O)C1 XBZSBBLNHFMTEB-UHFFFAOYSA-N 0.000 description 1
FOTKYAAJKYLFFN-UHFFFAOYSA-N decane-1,10-diol Chemical compound OCCCCCCCCCCO FOTKYAAJKYLFFN-UHFFFAOYSA-N 0.000 description 1
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 1
150000001991 dicarboxylic acids Chemical group 0.000 description 1
150000001993 dienes Chemical class 0.000 description 1
150000005690 diesters Chemical class 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
150000002009 diols Chemical class 0.000 description 1
239000000975 dye Substances 0.000 description 1
UIWXSTHGICQLQT-UHFFFAOYSA-N ethenyl propanoate Chemical compound CCC(=O)OC=C UIWXSTHGICQLQT-UHFFFAOYSA-N 0.000 description 1
125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
229940117927 ethylene oxide Drugs 0.000 description 1
238000011156 evaluation Methods 0.000 description 1
238000010101 extrusion blow moulding Methods 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
239000000835 fiber Substances 0.000 description 1
239000000945 filler Substances 0.000 description 1
239000003063 flame retardant Substances 0.000 description 1
125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 1
VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 description 1
125000005843 halogen group Chemical group 0.000 description 1
239000012760 heat stabilizer Substances 0.000 description 1
AHAREKHAZNPPMI-UHFFFAOYSA-N hexa-1,3-diene Chemical compound CCC=CC=C AHAREKHAZNPPMI-UHFFFAOYSA-N 0.000 description 1
XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
239000008240 homogeneous mixture Substances 0.000 description 1
150000002430 hydrocarbons Chemical group 0.000 description 1
229910052739 hydrogen Inorganic materials 0.000 description 1
239000001257 hydrogen Substances 0.000 description 1
125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
239000000314 lubricant Substances 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
239000011976 maleic acid Substances 0.000 description 1
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
125000005395 methacrylic acid group Chemical class 0.000 description 1
238000002156 mixing Methods 0.000 description 1
239000006082 mold release agent Substances 0.000 description 1
125000005487 naphthalate group Chemical group 0.000 description 1
DFFZOPXDTCDZDP-UHFFFAOYSA-N naphthalene-1,5-dicarboxylic acid Chemical compound C1=CC=C2C(C(=O)O)=CC=CC2=C1C(O)=O DFFZOPXDTCDZDP-UHFFFAOYSA-N 0.000 description 1
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 1
125000001624 naphthyl group Chemical group 0.000 description 1
SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
239000002667 nucleating agent Substances 0.000 description 1
125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
239000011574 phosphorus Substances 0.000 description 1
239000000049 pigment Substances 0.000 description 1
229920000647 polyepoxide Polymers 0.000 description 1
229920000139 polyethylene terephthalate Polymers 0.000 description 1
239000005020 polyethylene terephthalate Substances 0.000 description 1
239000012744 reinforcing agent Substances 0.000 description 1
229920005989 resin Polymers 0.000 description 1
239000011347 resin Substances 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000007790 solid phase Substances 0.000 description 1
239000000243 solution Substances 0.000 description 1
239000007858 starting material Substances 0.000 description 1
125000003944 tolyl group Chemical group 0.000 description 1
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
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 1
QEDNBHNWMHJNAB-UHFFFAOYSA-N tris(8-methylnonyl) phosphite Chemical compound CC(C)CCCCCCCOP(OCCCCCCCC(C)C)OCCCCCCCC(C)C QEDNBHNWMHJNAB-UHFFFAOYSA-N 0.000 description 1
KOZCZZVUFDCZGG-UHFFFAOYSA-N vinyl benzoate Chemical compound C=COC(=O)C1=CC=CC=C1 KOZCZZVUFDCZGG-UHFFFAOYSA-N 0.000 description 1
229920001567 vinyl ester resin Polymers 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1

Landscapes

Compositions Of Macromolecular Compounds (AREA)

JP7240278A 1978-06-15 1978-06-15 Aromatic polyester composition Granted JPS54162750A (en)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
JP7240278A JPS54162750A (en)	1978-06-15	1978-06-15	Aromatic polyester composition

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP7240278A JPS54162750A (en)	1978-06-15	1978-06-15	Aromatic polyester composition

Publications (2)

Publication Number	Publication Date
JPS54162750A JPS54162750A (en)	1979-12-24
JPS6347748B2 true JPS6347748B2 (sv)	1988-09-26

Family

ID=13488239

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP7240278A Granted JPS54162750A (en)	1978-06-15	1978-06-15	Aromatic polyester composition

Country Status (1)

Country	Link
JP (1)	JPS54162750A (sv)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPH0725851U (ja) *	1993-10-25	1995-05-16	長岡産業株式会社	座席クッション材

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPH0627248B2 (ja) *	1984-02-15	1994-04-13	東レ株式会社	ポリエステルブロツク共重合体組成物
JPS6112745A (ja) *	1984-06-27	1986-01-21	Toray Ind Inc	ポリブチレンテレフタレ−ト中空成形品
JPS6281444A (ja) *	1985-10-04	1987-04-14	Toyobo Co Ltd	熱可塑性樹脂組成物
EP0376851A3 (en) *	1988-12-29	1991-06-26	Cytogen Corporation	Molecular recognition units
JP3210702B2 (ja) *	1991-10-23	2001-09-17	ポリプラスチックス株式会社	ブロー成形用ポリエステル樹脂組成物及びその成形品

Citations (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS4837330A (sv) *	1971-09-16	1973-06-01
JPS4935458A (sv) *	1972-08-07	1974-04-02
JPS4944952A (sv) *	1972-09-05	1974-04-27
JPS51102042A (ja) *	1975-03-05	1976-09-09	Unitika Ltd	Jushisoseibutsu
JPS5219797A (en) *	1975-08-06	1977-02-15	Basf Ag	Thermoplastic molding material
JPS5232045A (en) *	1975-09-08	1977-03-10	Toray Ind Inc	Resin composition

1978
- 1978-06-15 JP JP7240278A patent/JPS54162750A/ja active Granted

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS4837330A (sv) *	1971-09-16	1973-06-01
JPS4935458A (sv) *	1972-08-07	1974-04-02
JPS4944952A (sv) *	1972-09-05	1974-04-27
JPS51102042A (ja) *	1975-03-05	1976-09-09	Unitika Ltd	Jushisoseibutsu
JPS5219797A (en) *	1975-08-06	1977-02-15	Basf Ag	Thermoplastic molding material
JPS5232045A (en) *	1975-09-08	1977-03-10	Toray Ind Inc	Resin composition

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPH0725851U (ja) *	1993-10-25	1995-05-16	長岡産業株式会社	座席クッション材

Also Published As

Publication number	Publication date
JPS54162750A (en)	1979-12-24

Publication	Publication Date	Title
US4292233A (en)	1981-09-29	High-impact polybutylene terephthalate
CA1166388A (en)	1984-04-24	Thermoplastic polyester moulding compositions containing grafted polyacrylates
US3937757A (en)	1976-02-10	Molding compositions of polybutylene terephthalate and olefin polymer
US3644574A (en)	1972-02-22	Shaped articles of blends of polyesters and polyvinyls
JPS641508B2 (sv)	1989-01-11
US4212791A (en)	1980-07-15	Poly(alkyleneterephthalate) molding compositions containing oligomeric polyester and segmented copolyester-polyether elastomer
EP0114288B1 (en)	1989-10-04	Additive concentrate for polyester compositions and method of addition
US4020122A (en)	1977-04-26	Process for the preparation of polyester compositions having increased melt elasticity
JPH0555551B2 (sv)	1993-08-17
CA1147894A (en)	1983-06-07	Thermoplastic polyesters, and method of making hollow articles therefrom
JP4600807B2 (ja)	2010-12-22	共重合ポリエステル樹脂及びこれを用いた成形製品
JPH0115534B2 (sv)	1989-03-17
JPS6347748B2 (sv)	1988-09-26
JPS6241256B2 (sv)	1987-09-02
JP2002532291A (ja)	2002-10-02	ポリマーの一軸スクリュー押出
US4454302A (en)	1984-06-12	Polyester resin composition
JPH06240121A (ja)	1994-08-30	熱可塑性樹脂組成物
JPS634565B2 (sv)	1988-01-29
JPH10152606A (ja)	1998-06-09	ポリエステル樹脂組成物及びその成形品
JPH0578584B2 (sv)	1993-10-29
JPS60170660A (ja)	1985-09-04	ポリエステルブロツク共重合体組成物
JPH04298528A (ja)	1992-10-22	ポリエステル樹脂
JPS62187756A (ja)	1987-08-17	ポリエステル成形材料
JP3320588B2 (ja)	2002-09-03	ポリエステル樹脂組成物
JPH05230350A (ja)	1993-09-07	ポリエステル系樹脂組成物およびその製造方法

JPS6347748B2 - - Google Patents

Info

Links

Landscapes

Priority Applications (1)

Applications Claiming Priority (1)

Publications (2)

Family

ID=13488239

Family Applications (1)

Country Status (1)

Cited By (1)

Families Citing this family (5)

Citations (6)

Patent Citations (6)

Cited By (1)

Also Published As

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