JPS6125142A - レントゲン写真フイルム支持体用着色ポリエステルフイルム - Google Patents

レントゲン写真フイルム支持体用着色ポリエステルフイルム

Info

Publication number: JPS6125142A
Authority: JP; Japan
Prior art keywords: film; group; polyester; ammonium salt; color tone
Prior art date: 1984-07-13
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.): Granted

Application number

JP14632484A

Other languages

English (en)

Japanese (ja)

Other versions

JPH042176B2 (2

Inventor

Toshiki Komaita

駒板　俊樹

Takanori Nakatate

中楯　隆徳

Yoshiyuki Funabashi

船橋　美行

Kazuto Kiyohara

一人清原

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.)

Konica Minolta Inc

Original Assignee

Konica Minolta 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.)

1984-07-13

Filing date

1984-07-13

Publication date

1986-02-04

1984-07-13 Application filed by Konica Minolta Inc filed Critical Konica Minolta Inc

1984-07-13 Priority to JP14632484A priority Critical patent/JPS6125142A/ja

1985-07-12 Priority to DE8585305018T priority patent/DE3579969D1/de

1985-07-12 Priority to US06/754,258 priority patent/US4628025A/en

1985-07-12 Priority to EP85305018A priority patent/EP0169039B1/en

1986-02-04 Publication of JPS6125142A publication Critical patent/JPS6125142A/ja

1992-01-16 Publication of JPH042176B2 publication Critical patent/JPH042176B2/ja

Status Granted legal-status Critical Current

Links

229920006267 polyester film Polymers 0.000 title claims abstract description 18
239000003086 colorant Substances 0.000 claims abstract description 20
150000003242 quaternary ammonium salts Chemical class 0.000 claims abstract description 11
125000000217 alkyl group Chemical group 0.000 claims abstract description 10
125000003545 alkoxy group Chemical group 0.000 claims abstract description 5
125000002768 hydroxyalkyl group Chemical group 0.000 claims abstract description 4
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract description 4
-1 aralkoxy group Chemical group 0.000 claims description 10
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 6
125000003277 amino group Chemical group 0.000 claims description 5
125000005336 allyloxy group Chemical group 0.000 claims description 2
125000005843 halogen group Chemical group 0.000 claims description 2
239000000126 substance Substances 0.000 claims 5
125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
229920000728 polyester Polymers 0.000 abstract description 20
230000015572 biosynthetic process Effects 0.000 abstract description 5
238000001125 extrusion Methods 0.000 abstract description 5
150000001450 anions Chemical group 0.000 abstract description 4
239000000155 melt Substances 0.000 abstract description 4
239000008188 pellet Substances 0.000 abstract description 3
150000003863 ammonium salts Chemical class 0.000 abstract description 2
125000003710 aryl alkyl group Chemical group 0.000 abstract description 2
125000003118 aryl group Chemical group 0.000 abstract description 2
239000011248 coating agent Substances 0.000 abstract description 2
238000000576 coating method Methods 0.000 abstract description 2
229910052736 halogen Inorganic materials 0.000 abstract description 2
150000002367 halogens Chemical class 0.000 abstract description 2
238000002360 preparation method Methods 0.000 abstract 2
125000000129 anionic group Chemical group 0.000 abstract 1
125000004104 aryloxy group Chemical group 0.000 abstract 1
238000004043 dyeing Methods 0.000 abstract 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
150000003866 tertiary ammonium salts Chemical class 0.000 abstract 1
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 16
238000000034 method Methods 0.000 description 15
235000019646 color tone Nutrition 0.000 description 14
150000001875 compounds Chemical class 0.000 description 9
238000004040 coloring Methods 0.000 description 7
238000006243 chemical reaction Methods 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
WOZVHXUHUFLZGK-UHFFFAOYSA-N dimethyl terephthalate Chemical compound COC(=O)C1=CC=C(C(=O)OC)C=C1 WOZVHXUHUFLZGK-UHFFFAOYSA-N 0.000 description 4
230000000694 effects Effects 0.000 description 4
229920001225 polyester resin Polymers 0.000 description 4
239000004645 polyester resin Substances 0.000 description 4
229920000642 polymer Polymers 0.000 description 4
238000003786 synthesis reaction Methods 0.000 description 4
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
125000004429 atom Chemical group 0.000 description 3
238000004519 manufacturing process Methods 0.000 description 3
238000000465 moulding Methods 0.000 description 3
QPFMBZIOSGYJDE-UHFFFAOYSA-N 1,1,2,2-tetrachloroethane Chemical compound ClC(Cl)C(Cl)Cl QPFMBZIOSGYJDE-UHFFFAOYSA-N 0.000 description 2
IBABXJRXGSAJLQ-UHFFFAOYSA-N 1,4-bis(2,6-diethyl-4-methylanilino)anthracene-9,10-dione Chemical compound CCC1=CC(C)=CC(CC)=C1NC(C=1C(=O)C2=CC=CC=C2C(=O)C=11)=CC=C1NC1=C(CC)C=C(C)C=C1CC IBABXJRXGSAJLQ-UHFFFAOYSA-N 0.000 description 2
FJKROLUGYXJWQN-UHFFFAOYSA-N 4-hydroxybenzoic acid Chemical compound OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 2
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
239000002253 acid Substances 0.000 description 2
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
ADCOVFLJGNWWNZ-UHFFFAOYSA-N antimony trioxide Chemical compound O=[Sb]O[Sb]=O ADCOVFLJGNWWNZ-UHFFFAOYSA-N 0.000 description 2
208000003464 asthenopia Diseases 0.000 description 2
WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
XQKKWWCELHKGKB-UHFFFAOYSA-L calcium acetate monohydrate Chemical compound O.[Ca+2].CC([O-])=O.CC([O-])=O XQKKWWCELHKGKB-UHFFFAOYSA-L 0.000 description 2
229910052799 carbon Inorganic materials 0.000 description 2
239000003054 catalyst Substances 0.000 description 2
150000001768 cations Chemical group 0.000 description 2
239000007795 chemical reaction product Substances 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
238000007796 conventional method Methods 0.000 description 2
125000004122 cyclic group Chemical group 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
239000006185 dispersion Substances 0.000 description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 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
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
238000006068 polycondensation reaction Methods 0.000 description 2
238000006116 polymerization reaction Methods 0.000 description 2
YPFDHNVEDLHUCE-UHFFFAOYSA-N propane-1,3-diol Chemical compound OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 2
229920005989 resin Polymers 0.000 description 2
239000011347 resin Substances 0.000 description 2
CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
239000000243 solution Substances 0.000 description 2
125000001424 substituent group Chemical group 0.000 description 2
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
238000005809 transesterification reaction Methods 0.000 description 2
ILWRPSCZWQJDMK-UHFFFAOYSA-N triethylazanium;chloride Chemical compound Cl.CCN(CC)CC ILWRPSCZWQJDMK-UHFFFAOYSA-N 0.000 description 2
230000000007 visual effect Effects 0.000 description 2
ZRPKEUVFESZUKX-UHFFFAOYSA-N 2-(2-hydroxyethoxy)benzoic acid Chemical compound OCCOC1=CC=CC=C1C(O)=O ZRPKEUVFESZUKX-UHFFFAOYSA-N 0.000 description 1
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
MMINFSMURORWKH-UHFFFAOYSA-N 3,6-dioxabicyclo[6.2.2]dodeca-1(10),8,11-triene-2,7-dione Chemical group O=C1OCCOC(=O)C2=CC=C1C=C2 MMINFSMURORWKH-UHFFFAOYSA-N 0.000 description 1
229940090248 4-hydroxybenzoic acid Drugs 0.000 description 1
239000005995 Aluminium silicate Substances 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
241000790917 Dioxys <bee> Species 0.000 description 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
239000004594 Masterbatch (MB) Substances 0.000 description 1
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
239000002202 Polyethylene glycol Substances 0.000 description 1
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
235000005811 Viola adunca Nutrition 0.000 description 1
240000009038 Viola odorata Species 0.000 description 1
235000013487 Viola odorata Nutrition 0.000 description 1
235000002254 Viola papilionacea Nutrition 0.000 description 1
239000000654 additive Substances 0.000 description 1
230000000996 additive effect Effects 0.000 description 1
239000001361 adipic acid Substances 0.000 description 1
235000011037 adipic acid Nutrition 0.000 description 1
125000002723 alicyclic group Chemical group 0.000 description 1
229910000147 aluminium phosphate Inorganic materials 0.000 description 1
235000012211 aluminium silicate Nutrition 0.000 description 1
229940058905 antimony compound for treatment of leishmaniasis and trypanosomiasis Drugs 0.000 description 1
150000001463 antimony compounds Chemical class 0.000 description 1
239000003963 antioxidant agent Substances 0.000 description 1
239000002216 antistatic agent Substances 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
239000001639 calcium acetate Substances 0.000 description 1
235000011092 calcium acetate Nutrition 0.000 description 1
229960005147 calcium acetate Drugs 0.000 description 1
229910000019 calcium carbonate Inorganic materials 0.000 description 1
229940043430 calcium compound Drugs 0.000 description 1
150000001674 calcium compounds Chemical class 0.000 description 1
125000004432 carbon atom Chemical group C* 0.000 description 1
150000001869 cobalt compounds Chemical class 0.000 description 1
239000000470 constituent Substances 0.000 description 1
230000007423 decrease Effects 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
238000004090 dissolution Methods 0.000 description 1
125000003438 dodecyl 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])C([H])([H])C([H])([H])* 0.000 description 1
230000032050 esterification Effects 0.000 description 1
238000005886 esterification reaction Methods 0.000 description 1
NGPZWOOKVNRELB-UHFFFAOYSA-N ethane-1,2-diol;methanol Chemical compound OC.OCCO NGPZWOOKVNRELB-UHFFFAOYSA-N 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
150000004665 fatty acids Chemical class 0.000 description 1
230000009477 glass transition Effects 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
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 1
239000012943 hotmelt Substances 0.000 description 1
230000001771 impaired effect Effects 0.000 description 1
150000002484 inorganic compounds Chemical class 0.000 description 1
229910010272 inorganic material Inorganic materials 0.000 description 1
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 1
150000002697 manganese compounds Chemical class 0.000 description 1
238000000691 measurement method Methods 0.000 description 1
KYTZHLUVELPASH-UHFFFAOYSA-N naphthalene-1,2-dicarboxylic acid Chemical class C1=CC=CC2=C(C(O)=O)C(C(=O)O)=CC=C21 KYTZHLUVELPASH-UHFFFAOYSA-N 0.000 description 1
125000001400 nonyl 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])C([H])([H])[H] 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
229910052698 phosphorus Inorganic materials 0.000 description 1
239000011574 phosphorus Substances 0.000 description 1
229920001515 polyalkylene glycol Polymers 0.000 description 1
229920001223 polyethylene glycol Polymers 0.000 description 1
229920000139 polyethylene terephthalate Polymers 0.000 description 1
239000005020 polyethylene terephthalate Substances 0.000 description 1
239000002904 solvent Substances 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
239000011550 stock solution Substances 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
150000003609 titanium compounds Chemical class 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
150000003752 zinc compounds Chemical class 0.000 description 1

Classifications

- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C1/00—Photosensitive materials
- G03C1/76—Photosensitive materials characterised by the base or auxiliary layers
- G03C1/825—Photosensitive materials characterised by the base or auxiliary layers characterised by antireflection means or visible-light filtering means, e.g. antihalation
- G03C1/83—Organic dyestuffs therefor
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C1/00—Photosensitive materials
- G03C1/76—Photosensitive materials characterised by the base or auxiliary layers
- G03C1/795—Photosensitive materials characterised by the base or auxiliary layers the base being of macromolecular substances
- G03C1/7954—Polyesters

Landscapes

Physics & Mathematics (AREA)
Chemical & Material Sciences (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
General Physics & Mathematics (AREA)
Spectroscopy & Molecular Physics (AREA)
Polyesters Or Polycarbonates (AREA)
Manufacture Of Macromolecular Shaped Articles (AREA)

JP14632484A 1984-07-13 1984-07-13 レントゲン写真フイルム支持体用着色ポリエステルフイルム Granted JPS6125142A (ja)

Priority Applications (4)

Application Number	Priority Date	Filing Date	Title
JP14632484A JPS6125142A (ja)	1984-07-13	1984-07-13	レントゲン写真フイルム支持体用着色ポリエステルフイルム
DE8585305018T DE3579969D1 (en)	1984-07-13	1985-07-12	Traeger fuer photographie.
US06/754,258 US4628025A (en)	1984-07-13	1985-07-12	Polyester support for photographic use
EP85305018A EP0169039B1 (en)	1984-07-13	1985-07-12	Support for photographic use

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP14632484A JPS6125142A (ja)	1984-07-13	1984-07-13	レントゲン写真フイルム支持体用着色ポリエステルフイルム

Publications (2)

Publication Number	Publication Date
JPS6125142A true JPS6125142A (ja)	1986-02-04
JPH042176B2 JPH042176B2 (2)	1992-01-16

Family

ID=15405093

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP14632484A Granted JPS6125142A (ja)	1984-07-13	1984-07-13	レントゲン写真フイルム支持体用着色ポリエステルフイルム

Country Status (4)

Country	Link
US (1)	US4628025A (2)
EP (1)	EP0169039B1 (2)
JP (1)	JPS6125142A (2)
DE (1)	DE3579969D1 (2)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
KR100326564B1 (ko) *	1995-03-16	2002-07-27	주식회사 코오롱	착색폴리에스테르필름및그의제조방법

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4847149A (en) *	1986-11-05	1989-07-11	Konica Corporation	Base for reflection-photographic elements
JPH01213642A (ja) *	1988-02-20	1989-08-28	Konica Corp	ハロゲン化銀写真感光材料の処理方法
JPH07168309A (ja) *	1993-12-16	1995-07-04	Fuji Photo Film Co Ltd	ハロゲン化銀写真感光材料
JP3406092B2 (ja) *	1994-10-28	2003-05-12	富士写真フイルム株式会社	写真用ポリエステル支持体の染色方法
EP2259136A1 (en) *	2009-06-03	2010-12-08	Carestream Health, Inc.	Film with blue dye
US8617801B2 (en)	2009-06-03	2013-12-31	Carestream Health, Inc.	Film with blue dye
CN104530745B (zh) *	2014-12-19	2017-02-01	江苏道博化工有限公司	一种制备溶剂紫38的方法

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3948664A (en) *	1968-08-21	1976-04-06	Fuji Photo Film Co., Ltd.	Polyethylene terephthalate film for use as support for radiographic film
JPS5443014B2 (2) *	1971-09-09	1979-12-18
JPS4910017A (2) *	1972-05-24	1974-01-29
JPS5941176B2 (ja) *	1979-04-23	1984-10-05	富士写真フイルム株式会社	写真用支持体

1984
- 1984-07-13 JP JP14632484A patent/JPS6125142A/ja active Granted
1985
- 1985-07-12 US US06/754,258 patent/US4628025A/en not_active Expired - Lifetime
- 1985-07-12 EP EP85305018A patent/EP0169039B1/en not_active Expired
- 1985-07-12 DE DE8585305018T patent/DE3579969D1/de not_active Expired - Fee Related

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
KR100326564B1 (ko) *	1995-03-16	2002-07-27	주식회사 코오롱	착색폴리에스테르필름및그의제조방법

Also Published As

Publication number	Publication date
EP0169039A3 (en)	1988-09-28
US4628025A (en)	1986-12-09
JPH042176B2 (2)	1992-01-16
DE3579969D1 (en)	1990-11-08
EP0169039B1 (en)	1990-10-03
EP0169039A2 (en)	1986-01-22

Publication	Publication Date	Title
US2901466A (en)	1959-08-25	Linear polyesters and polyester-amides from 1,4-cyclohexanedimethanol
DE2222145C3 (de)	1979-03-29	Verwendung von linearen Polymeren mit 1,1'-Spirobl [indan] -einheiten zur Herstellung von photographischen Schichtträgern
US4745174A (en)	1988-05-17	Polyesters having improved whiteness
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DE2342415A1 (de)	1974-03-07	Neue, lineare homo- und copolyester auf basis von tere- und/oder isophthalsaeure
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US6037393A (en)	2000-03-14	Compound, a process for the preparation thereof, and a resin composition
JPH06505514A (ja)	1994-06-23	写真ロールフィルム支持体として有用な変性ポリエステル
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US5188774A (en)	1993-02-23	Aromatic polyester film and process for producing the same
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JPH06104718B2 (ja)	1994-12-21	ポリエステルの製造方法
US3164569A (en)	1965-01-05	Linear polyesters of a glycol containing a p-dioxane ring
JPS5845451B2 (ja)	1983-10-11	線状熱可塑性コポリエステルの製造法
JP2005194499A (ja)	2005-07-21	マスターバッチ用熱可塑性樹脂組成物およびその成形材料の製造方法およびそれらを用いた熱可塑性樹脂組成物およびその製造方法
JPS6334178B2 (2)	1988-07-08
JP7771824B2 (ja)	2025-11-18	ポリエチレンテレフタレート樹脂組成物、ポリエステルフィルムおよびポリエチレンテレフタレート樹脂組成物の製造方法

JPS6125142A - レントゲン写真フイルム支持体用着色ポリエステルフイルム - Google Patents

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