JPH0466259B2 - - Google Patents
Info
- Publication number
- JPH0466259B2 JPH0466259B2 JP23804686A JP23804686A JPH0466259B2 JP H0466259 B2 JPH0466259 B2 JP H0466259B2 JP 23804686 A JP23804686 A JP 23804686A JP 23804686 A JP23804686 A JP 23804686A JP H0466259 B2 JPH0466259 B2 JP H0466259B2
- Authority
- JP
- Japan
- Prior art keywords
- formula
- polyesterimide
- dicarboxylic acid
- reaction
- acid
- 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
Links
- 229920003055 poly(ester-imide) Polymers 0.000 claims description 21
- 229920000642 polymer Polymers 0.000 claims description 9
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 15
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 12
- 150000001875 compounds Chemical class 0.000 description 11
- 125000003118 aryl group Chemical group 0.000 description 10
- 238000006243 chemical reaction Methods 0.000 description 8
- -1 aliphatic diamine Chemical class 0.000 description 6
- 238000000465 moulding Methods 0.000 description 5
- QPFMBZIOSGYJDE-UHFFFAOYSA-N 1,1,2,2-tetrachloroethane Chemical compound ClC(Cl)C(Cl)Cl QPFMBZIOSGYJDE-UHFFFAOYSA-N 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 4
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 229920006351 engineering plastic Polymers 0.000 description 4
- 238000002844 melting Methods 0.000 description 4
- 230000008018 melting Effects 0.000 description 4
- SRPWOOOHEPICQU-UHFFFAOYSA-N trimellitic anhydride Chemical compound OC(=O)C1=CC=C2C(=O)OC(=O)C2=C1 SRPWOOOHEPICQU-UHFFFAOYSA-N 0.000 description 4
- 239000007795 chemical reaction product Substances 0.000 description 3
- 150000001991 dicarboxylic acids Chemical class 0.000 description 3
- 150000002009 diols Chemical class 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- BGNXCDMCOKJUMV-UHFFFAOYSA-N Tert-Butylhydroquinone Chemical compound CC(C)(C)C1=CC(O)=CC=C1O BGNXCDMCOKJUMV-UHFFFAOYSA-N 0.000 description 2
- 238000005452 bending Methods 0.000 description 2
- 235000010290 biphenyl Nutrition 0.000 description 2
- 239000004305 biphenyl Substances 0.000 description 2
- YHWCPXVTRSHPNY-UHFFFAOYSA-N butan-1-olate;titanium(4+) Chemical compound [Ti+4].CCCC[O-].CCCC[O-].CCCC[O-].CCCC[O-] YHWCPXVTRSHPNY-UHFFFAOYSA-N 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
- 239000000945 filler Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000001746 injection moulding Methods 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
- 238000000034 method Methods 0.000 description 2
- 239000012046 mixed solvent Substances 0.000 description 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 2
- 230000007704 transition Effects 0.000 description 2
- ARCGXLSVLAOJQL-UHFFFAOYSA-N trimellitic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C(C(O)=O)=C1 ARCGXLSVLAOJQL-UHFFFAOYSA-N 0.000 description 2
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 1
- 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 1
- NEQFBGHQPUXOFH-UHFFFAOYSA-N 4-(4-carboxyphenyl)benzoic acid Chemical compound C1=CC(C(=O)O)=CC=C1C1=CC=C(C(O)=O)C=C1 NEQFBGHQPUXOFH-UHFFFAOYSA-N 0.000 description 1
- KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical compound NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 229920006125 amorphous polymer Polymers 0.000 description 1
- 150000004984 aromatic diamines Chemical class 0.000 description 1
- 150000007860 aryl ester derivatives Chemical class 0.000 description 1
- 238000006664 bond formation reaction Methods 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
- 125000003262 carboxylic acid ester group Chemical class [H]C([H])([*:2])OC(=O)C([H])([H])[*:1] 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- 125000001142 dicarboxylic acid group Chemical group 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000012456 homogeneous solution Substances 0.000 description 1
- 150000003949 imides Chemical group 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000000155 melt Substances 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
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
Landscapes
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP23804686A JPS6392651A (ja) | 1986-10-08 | 1986-10-08 | ポリエステルイミド |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP23804686A JPS6392651A (ja) | 1986-10-08 | 1986-10-08 | ポリエステルイミド |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6392651A JPS6392651A (ja) | 1988-04-23 |
| JPH0466259B2 true JPH0466259B2 (sv) | 1992-10-22 |
Family
ID=17024359
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP23804686A Granted JPS6392651A (ja) | 1986-10-08 | 1986-10-08 | ポリエステルイミド |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6392651A (sv) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5102978A (en) * | 1990-04-16 | 1992-04-07 | The Goodyear Tire & Rubber Company | Copolyester |
| WO1995031496A1 (en) * | 1994-05-17 | 1995-11-23 | E.I. Du Pont De Nemours And Company | Liquid crystalline poly(ester-imides) |
| JP2008063517A (ja) * | 2006-09-11 | 2008-03-21 | Asahi Kasei Corp | ポリエステルイミドおよびその製造方法 |
-
1986
- 1986-10-08 JP JP23804686A patent/JPS6392651A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6392651A (ja) | 1988-04-23 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP0252415B1 (en) | Novel polyester polymers | |
| EP0421603B1 (en) | Melt-processable copolyesterimide | |
| JPH0466259B2 (sv) | ||
| US3440218A (en) | Poly(amide-esters) of aromatic compounds | |
| EP4028450B1 (en) | Polyamide-imide polymer and process for its manufacture | |
| US6806346B2 (en) | Copolymerization of cyclic ester oligomers | |
| JPH0356527A (ja) | 芳香族ポリエステル及びその製造方法 | |
| JP2866125B2 (ja) | 芳香族ポリエステル共重合体 | |
| JPH04130131A (ja) | 加工が容易な全芳香族ポリエステル | |
| JPH03255124A (ja) | 芳香族ポリエステルアミド共重合体およびその製造法 | |
| JP3185414B2 (ja) | 芳香族コポリエステルイミド | |
| JPH039922A (ja) | 溶融加工性熱互変芳香族コポリエステル類およびその製造方法 | |
| JPH0381322A (ja) | ｓ‐トリアジン誘導体に基づく異方性ポリマー | |
| JP3071588B2 (ja) | 樹脂組成物 | |
| JPH08295734A (ja) | ポリイミド系樹脂およびその製法 | |
| JPS63146927A (ja) | 芳香族コポリエステルアミド | |
| JP2509252B2 (ja) | 新規共重合体とその製造法 | |
| JP2672426B2 (ja) | 樹脂組成物 | |
| JPH01266138A (ja) | ポリマー組成物およびその製法 | |
| JPH0531890B2 (sv) | ||
| JPH01138226A (ja) | 芳香族ポリエステル | |
| JPH05295110A (ja) | 新規ポリアミド及びその製造方法 | |
| JPH0579246B2 (sv) | ||
| JPH05148350A (ja) | 新規芳香族ポリエステル | |
| JPS63258927A (ja) | ポリアミドイミド |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| LAPS | Cancellation because of no payment of annual fees |