JPH0326697B2 - - Google Patents
Info
- Publication number
- JPH0326697B2 JPH0326697B2 JP59075038A JP7503884A JPH0326697B2 JP H0326697 B2 JPH0326697 B2 JP H0326697B2 JP 59075038 A JP59075038 A JP 59075038A JP 7503884 A JP7503884 A JP 7503884A JP H0326697 B2 JPH0326697 B2 JP H0326697B2
- Authority
- JP
- Japan
- Prior art keywords
- polyester
- reaction
- formula
- mol
- added
- Prior art date
- 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 - Lifetime
Links
- 229920000728 polyester Polymers 0.000 claims description 60
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 59
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 claims description 30
- 150000001875 compounds Chemical class 0.000 claims description 22
- 238000005809 transesterification reaction Methods 0.000 claims description 21
- 238000005886 esterification reaction Methods 0.000 claims description 19
- 238000006068 polycondensation reaction Methods 0.000 claims description 18
- 125000005647 linker group Chemical group 0.000 claims description 16
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 11
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 10
- 239000007795 chemical reaction product Substances 0.000 claims description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
- 238000009987 spinning Methods 0.000 description 22
- 239000000835 fiber Substances 0.000 description 20
- 229920000642 polymer Polymers 0.000 description 17
- WOZVHXUHUFLZGK-UHFFFAOYSA-N dimethyl terephthalate Chemical compound COC(=O)C1=CC=C(C(=O)OC)C=C1 WOZVHXUHUFLZGK-UHFFFAOYSA-N 0.000 description 10
- -1 polyethylene terephthalate Polymers 0.000 description 10
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- 238000000034 method Methods 0.000 description 9
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 8
- 239000002253 acid Substances 0.000 description 7
- 239000003054 catalyst Substances 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 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 4
- ADCOVFLJGNWWNZ-UHFFFAOYSA-N antimony trioxide Chemical compound O=[Sb]O[Sb]=O ADCOVFLJGNWWNZ-UHFFFAOYSA-N 0.000 description 4
- 238000007334 copolymerization reaction Methods 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 229910052698 phosphorus Inorganic materials 0.000 description 4
- 239000011574 phosphorus Substances 0.000 description 4
- 239000002994 raw material Substances 0.000 description 4
- 239000003381 stabilizer Substances 0.000 description 4
- 125000005907 alkyl ester group Chemical group 0.000 description 3
- 230000032050 esterification Effects 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 238000002074 melt spinning Methods 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 229920000139 polyethylene terephthalate Polymers 0.000 description 3
- 239000005020 polyethylene terephthalate Substances 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 238000004804 winding Methods 0.000 description 3
- BSYNRYMUTXBXSQ-UHFFFAOYSA-N Aspirin Chemical compound CC(=O)OC1=CC=CC=C1C(O)=O BSYNRYMUTXBXSQ-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 229940058905 antimony compound for treatment of leishmaniasis and trypanosomiasis Drugs 0.000 description 2
- 150000001463 antimony compounds Chemical class 0.000 description 2
- 230000001588 bifunctional effect Effects 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000002425 crystallisation Methods 0.000 description 2
- 230000008025 crystallization Effects 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- PGJQPLVEUVHSFQ-UHFFFAOYSA-N methyl-4-acetoxybenzoate Chemical compound COC(=O)C1=CC=C(OC(C)=O)C=C1 PGJQPLVEUVHSFQ-UHFFFAOYSA-N 0.000 description 2
- 239000012299 nitrogen atmosphere Substances 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- WVLBCYQITXONBZ-UHFFFAOYSA-N trimethyl phosphate Chemical compound COP(=O)(OC)OC WVLBCYQITXONBZ-UHFFFAOYSA-N 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 238000005160 1H NMR spectroscopy Methods 0.000 description 1
- ISPYQTSUDJAMAB-UHFFFAOYSA-N 2-chlorophenol Chemical compound OC1=CC=CC=C1Cl ISPYQTSUDJAMAB-UHFFFAOYSA-N 0.000 description 1
- 101100425597 Solanum lycopersicum Tm-1 gene Proteins 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 229940043430 calcium compound Drugs 0.000 description 1
- 150000001674 calcium compounds Chemical class 0.000 description 1
- 239000007809 chemical reaction catalyst Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 150000001869 cobalt compounds Chemical class 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 150000005690 diesters Chemical class 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- 238000010036 direct spinning Methods 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- ACGYGMKFCVDVHS-UHFFFAOYSA-N ethyl 4-acetyloxybenzoate Chemical compound CCOC(=O)C1=CC=C(OC(C)=O)C=C1 ACGYGMKFCVDVHS-UHFFFAOYSA-N 0.000 description 1
- NUVBSKCKDOMJSU-UHFFFAOYSA-N ethylparaben Chemical compound CCOC(=O)C1=CC=C(O)C=C1 NUVBSKCKDOMJSU-UHFFFAOYSA-N 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 150000002291 germanium compounds Chemical class 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 239000005457 ice water Substances 0.000 description 1
- 150000002681 magnesium compounds Chemical class 0.000 description 1
- 229940071125 manganese acetate Drugs 0.000 description 1
- 150000002697 manganese compounds Chemical class 0.000 description 1
- UOGMEBQRZBEZQT-UHFFFAOYSA-L manganese(2+);diacetate Chemical compound [Mn+2].CC([O-])=O.CC([O-])=O UOGMEBQRZBEZQT-UHFFFAOYSA-L 0.000 description 1
- LXCFILQKKLGQFO-UHFFFAOYSA-N methylparaben Chemical compound COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 description 1
- 239000012046 mixed solvent Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 150000003018 phosphorus compounds Chemical class 0.000 description 1
- 238000012805 post-processing Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 description 1
- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 150000003609 titanium compounds Chemical class 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 238000011282 treatment Methods 0.000 description 1
- 150000005691 triesters Chemical class 0.000 description 1
- 150000003752 zinc compounds Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/78—Preparation processes
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
- C08G63/60—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from the reaction of a mixture of hydroxy carboxylic acids, polycarboxylic acids and polyhydroxy compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polyesters Or Polycarbonates (AREA)
Description
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Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP59075038A JPS60219224A (ja) | 1984-04-16 | 1984-04-16 | ããªãšã¹ãã«ã®è£œé æ¹æ³ |
EP85302575A EP0159875B1 (en) | 1984-04-16 | 1985-04-12 | Polyester and process for preparation thereof |
DE8585302575T DE3580783D1 (de) | 1984-04-16 | 1985-04-12 | Polyester und verfahren zu dessen herstellung. |
US06/723,367 US4663423A (en) | 1984-04-16 | 1985-04-15 | Polyester and process for preparation thereof |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP59075038A JPS60219224A (ja) | 1984-04-16 | 1984-04-16 | ããªãšã¹ãã«ã®è£œé æ¹æ³ |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS60219224A JPS60219224A (ja) | 1985-11-01 |
JPH0326697B2 true JPH0326697B2 (ja) | 1991-04-11 |
Family
ID=13564631
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP59075038A Granted JPS60219224A (ja) | 1984-04-16 | 1984-04-16 | ããªãšã¹ãã«ã®è£œé æ¹æ³ |
Country Status (4)
Country | Link |
---|---|
US (1) | US4663423A (ja) |
EP (1) | EP0159875B1 (ja) |
JP (1) | JPS60219224A (ja) |
DE (1) | DE3580783D1 (ja) |
Families Citing this family (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5969079A (en) | 1985-09-05 | 1999-10-19 | The Boeing Company | Oligomers with multiple chemically functional end caps |
US5693741A (en) | 1988-03-15 | 1997-12-02 | The Boeing Company | Liquid molding compounds |
US5512676A (en) | 1987-09-03 | 1996-04-30 | The Boeing Company | Extended amideimide hub for multidimensional oligomers |
US5516876A (en) | 1983-09-27 | 1996-05-14 | The Boeing Company | Polyimide oligomers and blends |
US5210213A (en) | 1983-06-17 | 1993-05-11 | The Boeing Company | Dimensional, crosslinkable oligomers |
US5705598A (en) | 1985-04-23 | 1998-01-06 | The Boeing Company | Polyester sulfone oligomers and blends |
US5714566A (en) | 1981-11-13 | 1998-02-03 | The Boeing Company | Method for making multiple chemically functional oligomers |
US5618907A (en) | 1985-04-23 | 1997-04-08 | The Boeing Company | Thallium catalyzed multidimensional ester oligomers |
JPH0749472B2 (ja) * | 1986-09-26 | 1995-05-31 | ããªãã©ã¹ããã¯ã¹æ ªåŒäŒç€Ÿ | ã³ããªãšã¹ãã«ã®è£œé æ¹æ³ |
US5817744A (en) | 1988-03-14 | 1998-10-06 | The Boeing Company | Phenylethynyl capped imides |
US5310859A (en) * | 1990-04-06 | 1994-05-10 | Mitsubishi Kasei Corporation | Liquid crystalline polyesters and methods for their production |
JP3038779B2 (ja) * | 1990-04-19 | 2000-05-08 | æ±æŽçŽ¡çžŸæ ªåŒäŒç€Ÿ | ããªãšã¹ãã«ç³»ç¹ç¶ã®è£œé æ¹æ³ |
US5692938A (en) * | 1996-12-20 | 1997-12-02 | Asten, Inc. | Polyester fiber with improved abrasion resistance |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5226593A (en) * | 1975-08-25 | 1977-02-28 | Toyobo Co Ltd | Process for preparing arylene ester polymers |
JPS5734123A (en) * | 1980-08-07 | 1982-02-24 | Teijin Ltd | Production of polyester |
JPS5742922A (en) * | 1980-08-27 | 1982-03-10 | Teijin Ltd | Spinning method of polyester fiber |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3288755A (en) * | 1964-02-19 | 1966-11-29 | Inventa Ag | Process for the manufacture of copolyetheresters |
US3804805A (en) * | 1972-12-01 | 1974-04-16 | Eastman Kodak Co | Copolyester prepared from polyethylene terephthalate and an acyloxy benzoic acid |
CA1012289A (en) * | 1972-09-28 | 1977-06-14 | Herbert F. Kuhfuss | Copolyester |
US4035356A (en) * | 1976-05-07 | 1977-07-12 | Eastman Kodak Company | Copolyester prepared from an acyloxybenzoic acid and polyethylene terephthalate modified with p-hydroxyethoxybenzoic acid |
EP0007732A1 (en) * | 1978-07-31 | 1980-02-06 | Imperial Chemical Industries Plc | Shaped articles of intractable polymers |
US4287332A (en) * | 1979-11-19 | 1981-09-01 | Eastman Kodak Company | Process for improving the chemical resistance of aromatic polyesters |
KR860000205B1 (ko) * | 1981-01-19 | 1986-03-03 | ìžêŒ¬ ë§ì€ë¯ž | ìì ìŒì ê°ë¥í íŽëŠ¬ìì€í 륎 ì¬ì |
US4446302A (en) * | 1982-07-14 | 1984-05-01 | Eastman Kodak Company | Electrostatographic developers comprising toners containing a polyester having p-hydroxybenzoic acid recurring units |
-
1984
- 1984-04-16 JP JP59075038A patent/JPS60219224A/ja active Granted
-
1985
- 1985-04-12 EP EP85302575A patent/EP0159875B1/en not_active Expired
- 1985-04-12 DE DE8585302575T patent/DE3580783D1/de not_active Expired - Lifetime
- 1985-04-15 US US06/723,367 patent/US4663423A/en not_active Expired - Fee Related
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5226593A (en) * | 1975-08-25 | 1977-02-28 | Toyobo Co Ltd | Process for preparing arylene ester polymers |
JPS5734123A (en) * | 1980-08-07 | 1982-02-24 | Teijin Ltd | Production of polyester |
JPS5742922A (en) * | 1980-08-27 | 1982-03-10 | Teijin Ltd | Spinning method of polyester fiber |
Also Published As
Publication number | Publication date |
---|---|
EP0159875A3 (en) | 1987-07-15 |
US4663423A (en) | 1987-05-05 |
DE3580783D1 (de) | 1991-01-17 |
EP0159875B1 (en) | 1990-12-05 |
JPS60219224A (ja) | 1985-11-01 |
EP0159875A2 (en) | 1985-10-30 |
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