JPS6354431A - ジアセチレン基含有ポリアミド成形体の製造方法 - Google Patents
ジアセチレン基含有ポリアミド成形体の製造方法Info
- Publication number
- JPS6354431A JPS6354431A JP19805186A JP19805186A JPS6354431A JP S6354431 A JPS6354431 A JP S6354431A JP 19805186 A JP19805186 A JP 19805186A JP 19805186 A JP19805186 A JP 19805186A JP S6354431 A JPS6354431 A JP S6354431A
- Authority
- JP
- Japan
- Prior art keywords
- group
- diacetylene
- molding
- formula
- substituted aromatic
- 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 37
- 239000004760 aramid Substances 0.000 title claims abstract description 15
- 229920003235 aromatic polyamide Polymers 0.000 title claims abstract description 15
- 238000000465 moulding Methods 0.000 title abstract description 19
- 125000003368 amide group Chemical group 0.000 claims abstract description 9
- 125000002029 aromatic hydrocarbon group Chemical group 0.000 claims abstract description 9
- 125000001183 hydrocarbyl group Chemical group 0.000 claims abstract description 8
- 238000006116 polymerization reaction Methods 0.000 claims abstract description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims description 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 5
- 239000000126 substance Substances 0.000 claims 1
- 239000004952 Polyamide Substances 0.000 abstract description 7
- 229920002647 polyamide Polymers 0.000 abstract description 7
- 150000001412 amines Chemical class 0.000 abstract description 6
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract description 6
- -1 carboxylic acid halide Chemical class 0.000 abstract description 6
- 150000001732 carboxylic acid derivatives Chemical class 0.000 abstract description 4
- 239000003960 organic solvent Substances 0.000 abstract description 4
- 239000000243 solution Substances 0.000 abstract description 4
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 abstract description 4
- 150000001733 carboxylic acid esters Chemical class 0.000 abstract description 3
- 239000003513 alkali Substances 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 239000011259 mixed solution Substances 0.000 abstract 1
- 238000000034 method Methods 0.000 description 25
- 238000006243 chemical reaction Methods 0.000 description 11
- 229920000642 polymer Polymers 0.000 description 11
- 239000000463 material Substances 0.000 description 9
- 230000009257 reactivity Effects 0.000 description 8
- 238000005452 bending Methods 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- 125000005843 halogen group Chemical group 0.000 description 5
- 239000002994 raw material Substances 0.000 description 5
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 238000004132 cross linking Methods 0.000 description 4
- 125000004433 nitrogen atom Chemical group N* 0.000 description 4
- 230000035484 reaction time Effects 0.000 description 4
- 238000003786 synthesis reaction Methods 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 125000003277 amino group Chemical group 0.000 description 3
- 230000002706 hydrostatic effect Effects 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 238000011160 research Methods 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 125000002723 alicyclic group Chemical group 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 125000004429 atom Chemical group 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
- 150000001735 carboxylic acids Chemical class 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 125000004093 cyano group Chemical group *C#N 0.000 description 2
- 125000004185 ester group Chemical group 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Chemical group CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 230000005284 excitation Effects 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
- 230000005855 radiation Effects 0.000 description 2
- 238000005096 rolling process Methods 0.000 description 2
- 230000002194 synthesizing effect Effects 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- 238000004566 IR spectroscopy Methods 0.000 description 1
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 238000001069 Raman spectroscopy Methods 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 150000001350 alkyl halides Chemical class 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 150000001721 carbon Chemical group 0.000 description 1
- 150000001244 carboxylic acid anhydrides Chemical class 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 238000000748 compression moulding Methods 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000012776 electronic material Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000012761 high-performance material Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 230000009878 intermolecular interaction Effects 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 238000000462 isostatic pressing Methods 0.000 description 1
- 229920002521 macromolecule Polymers 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000008204 material by function Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 230000015654 memory Effects 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 238000001225 nuclear magnetic resonance method Methods 0.000 description 1
- 239000012766 organic filler Substances 0.000 description 1
- 238000005691 oxidative coupling reaction Methods 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 229920000015 polydiacetylene Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 230000001568 sexual effect Effects 0.000 description 1
- 239000007790 solid phase Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- YBBRCQOCSYXUOC-UHFFFAOYSA-N sulfuryl dichloride Chemical class ClS(Cl)(=O)=O YBBRCQOCSYXUOC-UHFFFAOYSA-N 0.000 description 1
- 238000002076 thermal analysis method Methods 0.000 description 1
Landscapes
- Casting Or Compression Moulding Of Plastics Or The Like (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Polyamides (AREA)
- Macromonomer-Based Addition Polymer (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP19805186A JPS6354431A (ja) | 1986-08-26 | 1986-08-26 | ジアセチレン基含有ポリアミド成形体の製造方法 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP19805186A JPS6354431A (ja) | 1986-08-26 | 1986-08-26 | ジアセチレン基含有ポリアミド成形体の製造方法 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6354431A true JPS6354431A (ja) | 1988-03-08 |
| JPH0338296B2 JPH0338296B2 (enrdf_load_html_response) | 1991-06-10 |
Family
ID=16384715
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP19805186A Granted JPS6354431A (ja) | 1986-08-26 | 1986-08-26 | ジアセチレン基含有ポリアミド成形体の製造方法 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6354431A (enrdf_load_html_response) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN107750238B (zh) * | 2015-05-15 | 2021-04-02 | 保罗·D·马诺斯 | 制备碱性水和酸性水的方法 |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62288628A (ja) * | 1986-06-06 | 1987-12-15 | Agency Of Ind Science & Technol | ジアセチレン基含有芳香族性ポリアミド |
-
1986
- 1986-08-26 JP JP19805186A patent/JPS6354431A/ja active Granted
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62288628A (ja) * | 1986-06-06 | 1987-12-15 | Agency Of Ind Science & Technol | ジアセチレン基含有芳香族性ポリアミド |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0338296B2 (enrdf_load_html_response) | 1991-06-10 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Chujo et al. | Reversible gelation of polyoxazoline by means of Diels-Alder reaction | |
| Wei et al. | Thermosensitive hydrogels synthesized by fast Diels–Alder reaction in water | |
| Wang et al. | Mechanically strong non-isocyanate polyurethane thermosets from cyclic carbonate linseed oil | |
| US4882399A (en) | Epoxy resins having reversible crosslinks | |
| Chen et al. | Thermo-and water-induced shape memory poly (vinyl alcohol) supramolecular networks crosslinked by self-complementary quadruple hydrogen bonding | |
| Nagasaki et al. | Primary amino-terminal heterobifunctional poly (ethylene oxide). Facile synthesis of poly (ethylene oxide) with a primary amino group at one end and a hydroxyl group at the other end | |
| Klein et al. | Poly (vinylsaccharide) s, 5. Synthesis and characterization of poly (vinylsaccharide) s of the amide type with disaccharides in the side chain | |
| JPH04227632A (ja) | 新規なポリエーテルアミド及びその製法 | |
| Qu et al. | Thermoset polyimide matrix resins with improved toughness and high Tg for high temperature carbon fiber composites | |
| JPS6354431A (ja) | ジアセチレン基含有ポリアミド成形体の製造方法 | |
| JPS61500851A (ja) | イソイミドを使用する共重合体及びその製造方法 | |
| JPH04122714A (ja) | 高分子量エポキシ樹脂の製造方法 | |
| CN116284760A (zh) | 一种聚酰胺弹性体及基于硫醇-迈克尔加成点击反应制备聚酰胺弹性体的方法 | |
| CN113636934A (zh) | 一种含缩醛键的多丙烯酸酯及其制备方法和应用 | |
| Hirn et al. | Linear precursors of liquid crystalline thermosets | |
| JPS6354430A (ja) | ジアセチレン基含有芳香族性ポリアミド成形体の製造方法 | |
| JPS63295612A (ja) | ２重結合を有するジアセチレン化合物を用いてなる高剛性成形体 | |
| JPS6354439A (ja) | ジアセチレン基及び非芳香族基含有ポリアミドの成形体 | |
| JPS62288611A (ja) | アミノ基含有ジアセチレン化合物を用いた成形品 | |
| JPS63145337A (ja) | 二重結合含有ジアセチレン系アミドオリゴマ−及びポリマ−を用いた成形体 | |
| JP2021042300A (ja) | ウレアポリマー | |
| JPS63295639A (ja) | ２重結合を有するジアセチレン化合物を用いてなる成形体 | |
| CN112625271A (zh) | 一种聚丙烯酰甘氨酰甘氨酰胺水凝胶及其制备方法 | |
| Lu et al. | Inverse thermally reversible gelation-based hydrogels: synthesis and characterization of N-isopropylacrylamide copolymers containing deoxycholic acid in the side chain | |
| JPH02604A (ja) | 含フッ素共重合体 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EXPY | Cancellation because of completion of term |