JPS6354438A - ジアセチレン基含有ポリイミド成形体 - Google Patents
ジアセチレン基含有ポリイミド成形体Info
- Publication number
- JPS6354438A JPS6354438A JP19804886A JP19804886A JPS6354438A JP S6354438 A JPS6354438 A JP S6354438A JP 19804886 A JP19804886 A JP 19804886A JP 19804886 A JP19804886 A JP 19804886A JP S6354438 A JPS6354438 A JP S6354438A
- Authority
- JP
- Japan
- Prior art keywords
- molding
- diacetylene
- group
- polyimide
- organic group
- 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.)
- Granted
Links
- LLCSWKVOHICRDD-UHFFFAOYSA-N buta-1,3-diyne Chemical group C#CC#C LLCSWKVOHICRDD-UHFFFAOYSA-N 0.000 title claims abstract description 15
- 239000004642 Polyimide Substances 0.000 title claims abstract description 11
- 229920001721 polyimide Polymers 0.000 title claims abstract description 11
- 238000000465 moulding Methods 0.000 title abstract description 28
- 125000000962 organic group Chemical group 0.000 claims abstract description 11
- 239000000126 substance Substances 0.000 claims abstract description 9
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- 229920000642 polymer Polymers 0.000 abstract description 7
- 229920005575 poly(amic acid) Polymers 0.000 abstract description 6
- 239000002904 solvent Substances 0.000 abstract description 6
- -1 tetracarboxylic acid compound Chemical class 0.000 abstract description 5
- 239000003795 chemical substances by application Substances 0.000 abstract description 4
- GTDPSWPPOUPBNX-UHFFFAOYSA-N ac1mqpva Chemical compound CC12C(=O)OC(=O)C1(C)C1(C)C2(C)C(=O)OC1=O GTDPSWPPOUPBNX-UHFFFAOYSA-N 0.000 abstract description 3
- 150000001408 amides Chemical class 0.000 abstract description 2
- 150000004985 diamines Chemical class 0.000 abstract description 2
- 150000003949 imides Chemical class 0.000 abstract 1
- 125000006158 tetracarboxylic acid group Chemical group 0.000 abstract 1
- 238000000034 method Methods 0.000 description 11
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 9
- 238000006116 polymerization reaction Methods 0.000 description 9
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 6
- 239000002253 acid Substances 0.000 description 5
- 239000003054 catalyst Substances 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- 238000007363 ring formation reaction Methods 0.000 description 4
- 229910021591 Copper(I) chloride Inorganic materials 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 3
- 125000001931 aliphatic group Chemical group 0.000 description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- OXBLHERUFWYNTN-UHFFFAOYSA-M copper(I) chloride Chemical compound [Cu]Cl OXBLHERUFWYNTN-UHFFFAOYSA-M 0.000 description 3
- 229940045803 cuprous chloride Drugs 0.000 description 3
- ANSXAPJVJOKRDJ-UHFFFAOYSA-N furo[3,4-f][2]benzofuran-1,3,5,7-tetrone Chemical compound C1=C2C(=O)OC(=O)C2=CC2=C1C(=O)OC2=O ANSXAPJVJOKRDJ-UHFFFAOYSA-N 0.000 description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- ITQTTZVARXURQS-UHFFFAOYSA-N 3-methylpyridine Chemical compound CC1=CC=CN=C1 ITQTTZVARXURQS-UHFFFAOYSA-N 0.000 description 2
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 125000002723 alicyclic group Chemical group 0.000 description 2
- 150000008064 anhydrides Chemical class 0.000 description 2
- 238000000748 compression moulding Methods 0.000 description 2
- ORTQZVOHEJQUHG-UHFFFAOYSA-L copper(II) chloride Chemical compound Cl[Cu]Cl ORTQZVOHEJQUHG-UHFFFAOYSA-L 0.000 description 2
- 238000005520 cutting process Methods 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 description 2
- 125000005843 halogen group Chemical group 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 238000005691 oxidative coupling reaction Methods 0.000 description 2
- 238000003825 pressing Methods 0.000 description 2
- 238000001308 synthesis method Methods 0.000 description 2
- OCJBOOLMMGQPQU-UHFFFAOYSA-N 1,4-dichlorobenzene Chemical compound ClC1=CC=C(Cl)C=C1 OCJBOOLMMGQPQU-UHFFFAOYSA-N 0.000 description 1
- OISVCGZHLKNMSJ-UHFFFAOYSA-N 2,6-Lutidine Substances CC1=CC=CC(C)=N1 OISVCGZHLKNMSJ-UHFFFAOYSA-N 0.000 description 1
- JHUUPUMBZGWODW-UHFFFAOYSA-N 3,6-dihydro-1,2-dioxine Chemical compound C1OOCC=C1 JHUUPUMBZGWODW-UHFFFAOYSA-N 0.000 description 1
- 238000004566 IR spectroscopy Methods 0.000 description 1
- KWYHDKDOAIKMQN-UHFFFAOYSA-N N,N,N',N'-tetramethylethylenediamine Chemical compound CN(C)CCN(C)C KWYHDKDOAIKMQN-UHFFFAOYSA-N 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 125000002029 aromatic hydrocarbon group Chemical group 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 238000012669 compression test Methods 0.000 description 1
- 150000001879 copper Chemical class 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 229960003280 cupric chloride Drugs 0.000 description 1
- 125000004093 cyano group Chemical group *C#N 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 229940117389 dichlorobenzene Drugs 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000012776 electronic material Substances 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 230000005284 excitation Effects 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical group 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 230000002706 hydrostatic effect Effects 0.000 description 1
- 125000005462 imide group Chemical group 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 238000002329 infrared spectrum Methods 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 238000003754 machining Methods 0.000 description 1
- 150000002696 manganese Chemical class 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 150000007530 organic bases Chemical class 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 238000006798 ring closing metathesis reaction Methods 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 125000001174 sulfone group Chemical group 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Heating, Cooling, Or Curing Plastics Or The Like In General (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
- Artificial Filaments (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP19804886A JPS6354438A (ja) | 1986-08-26 | 1986-08-26 | ジアセチレン基含有ポリイミド成形体 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP19804886A JPS6354438A (ja) | 1986-08-26 | 1986-08-26 | ジアセチレン基含有ポリイミド成形体 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6354438A true JPS6354438A (ja) | 1988-03-08 |
| JPH0513975B2 JPH0513975B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1993-02-23 |
Family
ID=16384664
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP19804886A Granted JPS6354438A (ja) | 1986-08-26 | 1986-08-26 | ジアセチレン基含有ポリイミド成形体 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6354438A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR100779986B1 (ko) | 2006-12-30 | 2007-11-28 | 한양대학교 산학협력단 | 폴리다이아세틸렌 함유 초미세섬유의 제조방법 |
| KR20190106987A (ko) | 2017-01-30 | 2019-09-18 | 쿠리타 고교 가부시키가이샤 | 전기 전도도에 의한 pH 제어 방법 |
-
1986
- 1986-08-26 JP JP19804886A patent/JPS6354438A/ja active Granted
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR100779986B1 (ko) | 2006-12-30 | 2007-11-28 | 한양대학교 산학협력단 | 폴리다이아세틸렌 함유 초미세섬유의 제조방법 |
| KR20190106987A (ko) | 2017-01-30 | 2019-09-18 | 쿠리타 고교 가부시키가이샤 | 전기 전도도에 의한 pH 제어 방법 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0513975B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1993-02-23 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| KR102070942B1 (ko) | 폴리이미드계 공중합체 및 이를 포함하는 폴리이미드계 필름 | |
| JPS63118330A (ja) | イソイミド含有オリゴマ− | |
| Zhang et al. | Synthesis, characterization, and curing kinetics of novel bismaleimide monomers containing fluorene cardo group and aryl ether linkage | |
| US4777237A (en) | Polymer from (1) bis-imide, (2) allyloxy-phenyl maleimide and (3) diamine | |
| JP2719538B2 (ja) | ビス（マレインイミド）―シロキサンを含有可能なマレインイミドとシロキサン―ジアミンとを基とする耐熱性ポリマーの製造方法 | |
| Melissaris et al. | Bismaleimides chain‐extended by imidized benzophenone tetracarboxylic dianhydride and their polymerization to high temperature matrix resins | |
| Wang et al. | Synthesis and properties of novel naphthalene‐containing bismaleimides | |
| JPH0345617A (ja) | 潜伏性マレインイミド官能基を含む基を鎖部の末端に官能基として含有する直鎖芳香族ポリ（アミド―イミド）、およびその製造方法 | |
| US4847343A (en) | Heat-resistant maleimido copolymers | |
| JPS6354438A (ja) | ジアセチレン基含有ポリイミド成形体 | |
| Bochenkov et al. | Novel thermosetting diimides containing terminal propargyl groups | |
| JP2597863B2 (ja) | ヒンダードジアミンから製造するイミド基含有重合体の製造方法 | |
| JPS6315827A (ja) | ジアセチレン基含有ポリアミド酸及びポリイミド | |
| JPS5952660B2 (ja) | ポリマレイミドの製造方法 | |
| JPH0586778B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
| JP2651219B2 (ja) | イミド環を含む硬化性樹脂の製造法 | |
| Hariharan et al. | Synthesis and properties of novel organosoluble bismaleimides and polyaspartimides containing bis (4‐maleimido‐3, 5‐dimethyl phenyl) halo phenyl methane | |
| JPH0786130B2 (ja) | ビス（イミド）及びアルケニルオキシアニリンからのイミド基含有重合体の製造方法 | |
| Spiliopoulos et al. | Unsaturated polyamides and polyesters prepared from 1, 4‐bis (2‐carboxyvinyl) benzene and 4‐hydroxycinnamic acid | |
| Yan et al. | Optical transparency and light colour of highly soluble fluorinated polyimides derived from a novel pyridine-containing diamine m, p-3FPAPP and various aromatic dianhydrides | |
| JP4035365B2 (ja) | 交互重合体型ポリイミドおよび交互重合体型ポリイミドの製造方法 | |
| JPH05271411A (ja) | イミドオリゴマ型耐熱性樹脂組成物およびその製造方法 | |
| Mikroyannidis | Laminating resins obtained from 2, 2′‐(1, 4‐phenylenedivinylene) bispyridine bismaleimides and maleimide‐terminated styrylpyridine prepolymers | |
| Gaina et al. | Synthesis of new polyimidosulfides by Michael addition of bis (1-mercapto-2-ethylether) and amido thiosulfide oligomers | |
| JPH05222192A (ja) | ポリイミド共重合体及びその製造方法 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EXPY | Cancellation because of completion of term |