CN105593302B - 聚芳硫醚树脂组合物及其成形品、以及电动汽车部件 - Google Patents
聚芳硫醚树脂组合物及其成形品、以及电动汽车部件 Download PDFInfo
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- CN105593302B CN105593302B CN201480054696.4A CN201480054696A CN105593302B CN 105593302 B CN105593302 B CN 105593302B CN 201480054696 A CN201480054696 A CN 201480054696A CN 105593302 B CN105593302 B CN 105593302B
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- polyarylene sulfide
- sulfide resin
- electric
- vehicle part
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- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- ABMFBCRYHDZLRD-UHFFFAOYSA-N naphthalene-1,4-dicarboxylic acid Chemical class C1=CC=C2C(C(=O)O)=CC=C(C(O)=O)C2=C1 ABMFBCRYHDZLRD-UHFFFAOYSA-N 0.000 description 1
- KQSABULTKYLFEV-UHFFFAOYSA-N naphthalene-1,5-diamine Chemical class C1=CC=C2C(N)=CC=CC2=C1N KQSABULTKYLFEV-UHFFFAOYSA-N 0.000 description 1
- RXOHFPCZGPKIRD-UHFFFAOYSA-N naphthalene-2,6-dicarboxylic acid Chemical class C1=C(C(O)=O)C=CC2=CC(C(=O)O)=CC=C21 RXOHFPCZGPKIRD-UHFFFAOYSA-N 0.000 description 1
- WPUMVKJOWWJPRK-UHFFFAOYSA-N naphthalene-2,7-dicarboxylic acid Chemical class C1=CC(C(O)=O)=CC2=CC(C(=O)O)=CC=C21 WPUMVKJOWWJPRK-UHFFFAOYSA-N 0.000 description 1
- 238000006396 nitration reaction Methods 0.000 description 1
- 150000002828 nitro derivatives Chemical class 0.000 description 1
- 229940038384 octadecane Drugs 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- PBLZLIFKVPJDCO-UHFFFAOYSA-N omega-Aminododecanoic acid Natural products NCCCCCCCCCCCC(O)=O PBLZLIFKVPJDCO-UHFFFAOYSA-N 0.000 description 1
- 235000010292 orthophenyl phenol Nutrition 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 125000005968 oxazolinyl group Chemical group 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- VHDHONCVIHDOAO-UHFFFAOYSA-N pentacosanedioic acid Chemical compound OC(=O)CCCCCCCCCCCCCCCCCCCCCCCC(O)=O VHDHONCVIHDOAO-UHFFFAOYSA-N 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 229920001643 poly(ether ketone) Polymers 0.000 description 1
- 229920002492 poly(sulfone) Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920006393 polyether sulfone Polymers 0.000 description 1
- 229920002530 polyetherether ketone Polymers 0.000 description 1
- 229920001601 polyetherimide Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920006124 polyolefin elastomer Polymers 0.000 description 1
- 229920006389 polyphenyl polymer Polymers 0.000 description 1
- 229920006380 polyphenylene oxide Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- CVVPSCOTSPAXLS-UHFFFAOYSA-N propylidenecyclohexane Chemical compound CCC=C1CCCCC1 CVVPSCOTSPAXLS-UHFFFAOYSA-N 0.000 description 1
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000007151 ring opening polymerisation reaction Methods 0.000 description 1
- 229910052701 rubidium Inorganic materials 0.000 description 1
- IGLNJRXAVVLDKE-UHFFFAOYSA-N rubidium atom Chemical compound [Rb] IGLNJRXAVVLDKE-UHFFFAOYSA-N 0.000 description 1
- 238000005070 sampling Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 238000010583 slow cooling Methods 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 229910052979 sodium sulfide Inorganic materials 0.000 description 1
- GRVFOGOEDUUMBP-UHFFFAOYSA-N sodium sulfide (anhydrous) Chemical compound [Na+].[Na+].[S-2] GRVFOGOEDUUMBP-UHFFFAOYSA-N 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 238000007655 standard test method Methods 0.000 description 1
- QAZLUNIWYYOJPC-UHFFFAOYSA-M sulfenamide Chemical compound [Cl-].COC1=C(C)C=[N+]2C3=NC4=CC=C(OC)C=C4N3SCC2=C1C QAZLUNIWYYOJPC-UHFFFAOYSA-M 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical compound FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 1
- ISXOBTBCNRIIQO-UHFFFAOYSA-N tetrahydrothiophene 1-oxide Chemical compound O=S1CCCC1 ISXOBTBCNRIIQO-UHFFFAOYSA-N 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- GVIJJXMXTUZIOD-UHFFFAOYSA-N thianthrene Chemical compound C1=CC=C2SC3=CC=CC=C3SC2=C1 GVIJJXMXTUZIOD-UHFFFAOYSA-N 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- SLGBZMMZGDRARJ-UHFFFAOYSA-N triphenylene Chemical compound C1=CC=C2C3=CC=CC=C3C3=CC=CC=C3C2=C1 SLGBZMMZGDRARJ-UHFFFAOYSA-N 0.000 description 1
- AAAQKTZKLRYKHR-UHFFFAOYSA-N triphenylmethane Chemical compound C1=CC=CC=C1C(C=1C=CC=CC=1)C1=CC=CC=C1 AAAQKTZKLRYKHR-UHFFFAOYSA-N 0.000 description 1
- LZTRCELOJRDYMQ-UHFFFAOYSA-N triphenylmethanol Chemical compound C=1C=CC=CC=1C(C=1C=CC=CC=1)(O)C1=CC=CC=C1 LZTRCELOJRDYMQ-UHFFFAOYSA-N 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
- 150000007934 α,β-unsaturated carboxylic acids 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
- C08G75/00—Macromolecular compounds obtained by reactions forming a linkage containing sulfur with or without nitrogen, oxygen, or carbon in the main chain of the macromolecule
- C08G75/02—Polythioethers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L81/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing sulfur with or without nitrogen, oxygen or carbon only; Compositions of polysulfones; Compositions of derivatives of such polymers
- C08L81/02—Polythioethers; Polythioether-ethers
-
- 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
- C08G75/00—Macromolecular compounds obtained by reactions forming a linkage containing sulfur with or without nitrogen, oxygen, or carbon in the main chain of the macromolecule
- C08G75/02—Polythioethers
- C08G75/0204—Polyarylenethioethers
-
- 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
- C08G75/00—Macromolecular compounds obtained by reactions forming a linkage containing sulfur with or without nitrogen, oxygen, or carbon in the main chain of the macromolecule
- C08G75/02—Polythioethers
- C08G75/0204—Polyarylenethioethers
- C08G75/025—Preparatory processes
- C08G75/0263—Preparatory processes using elemental sulfur
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/01—Use of inorganic substances as compounding ingredients characterized by their specific function
- C08K3/013—Fillers, pigments or reinforcing additives
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L101/00—Compositions of unspecified macromolecular compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2203/00—Applications
- C08L2203/20—Applications use in electrical or conductive gadgets
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
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| CN201811014585.7A CN109096761B (zh) | 2013-10-01 | 2014-08-28 | 聚芳硫醚树脂组合物及其成形品、以及电动汽车部件 |
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| JP2013206459 | 2013-10-01 | ||
| JP2013-206459 | 2013-10-01 | ||
| PCT/JP2014/072641 WO2015049941A1 (fr) | 2013-10-01 | 2014-08-28 | Composition de résine de poly(sulfure d'arylène) et produit moulé en cette dernière, et pièce de véhicule électrique |
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| CN201480054696.4A Active CN105593302B (zh) | 2013-10-01 | 2014-08-28 | 聚芳硫醚树脂组合物及其成形品、以及电动汽车部件 |
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Country Status (4)
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| JP (1) | JP6444879B2 (fr) |
| KR (3) | KR102668078B1 (fr) |
| CN (2) | CN109096761B (fr) |
| WO (1) | WO2015049941A1 (fr) |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| KR102300453B1 (ko) * | 2015-05-14 | 2021-09-09 | 에스케이케미칼 주식회사 | 금속과의 접착성이 우수한 폴리아릴렌 설파이드 조성물 |
| US20180346721A1 (en) * | 2015-11-23 | 2018-12-06 | Sk Chemicals Co., Ltd. | Polyarylene sulfide resin composition and molded article |
| US10822457B2 (en) | 2015-11-23 | 2020-11-03 | Sk Chemicals Co., Ltd. | Polyarylene sulfide resin and preparation method thereof |
| JP6742109B2 (ja) * | 2016-02-23 | 2020-08-19 | 帝人株式会社 | 樹脂組成物 |
| JP6885096B2 (ja) * | 2016-02-26 | 2021-06-09 | 東レ株式会社 | ポリフェニレンスルフィド樹脂組成物および成形品 |
| CN109705346A (zh) * | 2018-12-29 | 2019-05-03 | 重庆晟淦新材料科技有限公司 | 不含氯化锂和添加剂的聚苯硫醚及其制备方法与应用 |
| CN114514117B (zh) * | 2019-11-19 | 2023-12-15 | Dic株式会社 | 双轴拉伸层叠膜、层叠体和它们的制造方法 |
| KR20210100814A (ko) * | 2020-02-07 | 2021-08-18 | 에스케이케미칼 주식회사 | 폴리아릴렌 설파이드 수지의 중합금지제 |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102325826A (zh) * | 2008-12-23 | 2012-01-18 | Sk化学株式会社 | 用于制备聚亚芳基硫醚的方法 |
| CN102762638A (zh) * | 2010-02-01 | 2012-10-31 | Sk化学株式会社 | 用于制备具有减少的碘含量的聚亚芳基硫醚的方法 |
| CN102791773A (zh) * | 2010-03-09 | 2012-11-21 | Sk化学株式会社 | 可重复利用的聚亚芳基硫醚及其制备方法 |
| US20130115438A1 (en) * | 2010-05-12 | 2013-05-09 | Sk Chemical Co., Ltd. | Polyarylene sulfide having excellent processability and preparation method thereof |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH06172489A (ja) * | 1992-12-08 | 1994-06-21 | Mitsubishi Petrochem Co Ltd | 熱可塑性樹脂組成物 |
| JP4269198B2 (ja) | 1998-07-30 | 2009-05-27 | Ｄｉｃ株式会社 | ポリアリーレンサルファイド樹脂組成物 |
| JP5029881B2 (ja) * | 2007-03-29 | 2012-09-19 | Ｄｉｃ株式会社 | ポリアリーレンスルフィド樹脂組成物 |
| KR101554010B1 (ko) * | 2008-12-31 | 2015-09-18 | 에스케이케미칼 주식회사 | 유리 요오드 저감 폴리아릴렌 설파이드의 제조 방법 |
| KR101944898B1 (ko) * | 2012-06-11 | 2019-02-01 | 에스케이케미칼 주식회사 | 폴리아릴렌 설파이드 수지 조성물 및 이의 제조 방법 |
| US20150197605A1 (en) * | 2012-08-07 | 2015-07-16 | Sk Chemicals Co., Ltd. | Polyarylene sulfide and a preparation method thereof |
| JP2015030779A (ja) * | 2013-08-01 | 2015-02-16 | 帝人株式会社 | 樹脂組成物 |
-
2014
- 2014-08-28 KR KR1020247002121A patent/KR102668078B1/ko active IP Right Grant
- 2014-08-28 KR KR1020167007982A patent/KR20160065836A/ko not_active IP Right Cessation
- 2014-08-28 CN CN201811014585.7A patent/CN109096761B/zh active Active
- 2014-08-28 WO PCT/JP2014/072641 patent/WO2015049941A1/fr active Application Filing
- 2014-08-28 KR KR1020227004201A patent/KR20220025152A/ko active Application Filing
- 2014-08-28 JP JP2015540428A patent/JP6444879B2/ja active Active
- 2014-08-28 CN CN201480054696.4A patent/CN105593302B/zh active Active
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102325826A (zh) * | 2008-12-23 | 2012-01-18 | Sk化学株式会社 | 用于制备聚亚芳基硫醚的方法 |
| CN102762638A (zh) * | 2010-02-01 | 2012-10-31 | Sk化学株式会社 | 用于制备具有减少的碘含量的聚亚芳基硫醚的方法 |
| CN102791773A (zh) * | 2010-03-09 | 2012-11-21 | Sk化学株式会社 | 可重复利用的聚亚芳基硫醚及其制备方法 |
| US20130115438A1 (en) * | 2010-05-12 | 2013-05-09 | Sk Chemical Co., Ltd. | Polyarylene sulfide having excellent processability and preparation method thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| CN109096761A (zh) | 2018-12-28 |
| KR20240013856A (ko) | 2024-01-30 |
| JP6444879B2 (ja) | 2018-12-26 |
| CN109096761B (zh) | 2021-05-11 |
| KR20220025152A (ko) | 2022-03-03 |
| CN105593302A (zh) | 2016-05-18 |
| JPWO2015049941A1 (ja) | 2017-03-09 |
| KR102668078B1 (ko) | 2024-05-23 |
| WO2015049941A1 (fr) | 2015-04-09 |
| KR20160065836A (ko) | 2016-06-09 |
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