ES2450123T3 - Combinados mejorados de poliarilenéteres y poli(sulfuros de arileno) - Google Patents
Combinados mejorados de poliarilenéteres y poli(sulfuros de arileno) Download PDFInfo
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- ES2450123T3 ES2450123T3 ES11708507.6T ES11708507T ES2450123T3 ES 2450123 T3 ES2450123 T3 ES 2450123T3 ES 11708507 T ES11708507 T ES 11708507T ES 2450123 T3 ES2450123 T3 ES 2450123T3
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- GTCCGKPBSJZVRZ-UHFFFAOYSA-N pentane-2,4-diol Chemical compound CC(O)CC(C)O GTCCGKPBSJZVRZ-UHFFFAOYSA-N 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 125000005561 phenanthryl group Chemical group 0.000 description 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
- CCDXIADKBDSBJU-UHFFFAOYSA-N phenylmethanetriol Chemical compound OC(O)(O)C1=CC=CC=C1 CCDXIADKBDSBJU-UHFFFAOYSA-N 0.000 description 1
- QCDYQQDYXPDABM-UHFFFAOYSA-N phloroglucinol Chemical compound OC1=CC(O)=CC(O)=C1 QCDYQQDYXPDABM-UHFFFAOYSA-N 0.000 description 1
- 150000003007 phosphonic acid derivatives Chemical group 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- HDOWRFHMPULYOA-UHFFFAOYSA-N piperidin-4-ol Chemical compound OC1CCNCC1 HDOWRFHMPULYOA-UHFFFAOYSA-N 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920001610 polycaprolactone Polymers 0.000 description 1
- 239000004632 polycaprolactone Substances 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920002959 polymer blend Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920000909 polytetrahydrofuran Polymers 0.000 description 1
- 229920000166 polytrimethylene carbonate Polymers 0.000 description 1
- 238000003918 potentiometric titration Methods 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 description 1
- AOHJOMMDDJHIJH-UHFFFAOYSA-N propylenediamine Chemical compound CC(N)CN AOHJOMMDDJHIJH-UHFFFAOYSA-N 0.000 description 1
- 238000011403 purification operation Methods 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000003252 repetitive effect Effects 0.000 description 1
- 238000007363 ring formation reaction Methods 0.000 description 1
- WWYDYZMNFQIYPT-UHFFFAOYSA-N ru78191 Chemical compound OC(=O)C(C(O)=O)C1=CC=CC=C1 WWYDYZMNFQIYPT-UHFFFAOYSA-N 0.000 description 1
- 150000003873 salicylate salts Chemical class 0.000 description 1
- 239000012266 salt solution Substances 0.000 description 1
- CDAISMWEOUEBRE-UHFFFAOYSA-N scyllo-inosotol Natural products OC1C(O)C(O)C(O)C(O)C1O CDAISMWEOUEBRE-UHFFFAOYSA-N 0.000 description 1
- 125000003548 sec-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 description 1
- 150000003336 secondary aromatic amines Chemical class 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 125000005373 siloxane group Chemical group [SiH2](O*)* 0.000 description 1
- 238000004513 sizing Methods 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 229910052596 spinel Inorganic materials 0.000 description 1
- 239000011029 spinel Substances 0.000 description 1
- 229920006301 statistical copolymer Polymers 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
- 235000000346 sugar Nutrition 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 1
- 150000003458 sulfonic acid derivatives Chemical group 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000009864 tensile test Methods 0.000 description 1
- DYHSDKLCOJIUFX-UHFFFAOYSA-N tert-butoxycarbonyl anhydride Chemical compound CC(C)(C)OC(=O)OC(=O)OC(C)(C)C DYHSDKLCOJIUFX-UHFFFAOYSA-N 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- IFLREYGFSNHWGE-UHFFFAOYSA-N tetracene Chemical compound C1=CC=CC2=CC3=CC4=CC=CC=C4C=C3C=C21 IFLREYGFSNHWGE-UHFFFAOYSA-N 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- 239000003017 thermal stabilizer Substances 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 150000003573 thiols Chemical class 0.000 description 1
- 229930192474 thiophene Natural products 0.000 description 1
- 150000003577 thiophenes Chemical class 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- 150000005691 triesters Chemical class 0.000 description 1
- YFHICDDUDORKJB-UHFFFAOYSA-N trimethylene carbonate Chemical compound O=C1OCCCO1 YFHICDDUDORKJB-UHFFFAOYSA-N 0.000 description 1
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
- GKODZWOPPOTFGA-UHFFFAOYSA-N tris(hydroxyethyl)aminomethane Chemical compound OCCC(N)(CCO)CCO GKODZWOPPOTFGA-UHFFFAOYSA-N 0.000 description 1
- 125000002948 undecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N urea group Chemical group NC(=O)N XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N urethane group Chemical group NC(=O)OCC JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 239000003981 vehicle Substances 0.000 description 1
- 229910052727 yttrium Inorganic materials 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- 229910052984 zinc sulfide Inorganic materials 0.000 description 1
- DGVVWUTYPXICAM-UHFFFAOYSA-N β‐Mercaptoethanol Chemical compound OCCS DGVVWUTYPXICAM-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L71/00—Compositions of polyethers obtained by reactions forming an ether link in the main chain; Compositions of derivatives of such polymers
- C08L71/08—Polyethers derived from hydroxy compounds or from their metallic derivatives
- C08L71/10—Polyethers derived from hydroxy compounds or from their metallic derivatives from phenols
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L71/00—Compositions of polyethers obtained by reactions forming an ether link in the main chain; Compositions of derivatives of such polymers
-
- 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
- C08L101/005—Dendritic macromolecules
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L69/00—Compositions of polycarbonates; Compositions of derivatives of polycarbonates
-
- 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
- C08L81/04—Polysulfides
-
- 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
- C08L81/06—Polysulfones; Polyethersulfones
-
- 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
- C08G2650/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G2650/28—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule characterised by the polymer type
- C08G2650/38—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule characterised by the polymer type containing oxygen in addition to the ether group
- C08G2650/40—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule characterised by the polymer type containing oxygen in addition to the ether group containing ketone groups, e.g. polyarylethylketones, PEEK or PEK
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/03—Polymer mixtures characterised by other features containing three or more polymers in a blend
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)
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP10157281 | 2010-03-23 | ||
| EP10157281 | 2010-03-23 | ||
| PCT/EP2011/054132 WO2011117153A1 (de) | 2010-03-23 | 2011-03-18 | Verbesserte blends aus polyarylenethern und polyarylensulfiden |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2450123T3 true ES2450123T3 (es) | 2014-03-24 |
Family
ID=44217499
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES11708507.6T Active ES2450123T3 (es) | 2010-03-23 | 2011-03-18 | Combinados mejorados de poliarilenéteres y poli(sulfuros de arileno) |
Country Status (7)
| Country | Link |
|---|---|
| EP (1) | EP2550335B1 (enExample) |
| JP (1) | JP5791697B2 (enExample) |
| KR (1) | KR20130019396A (enExample) |
| CN (1) | CN102834464B (enExample) |
| BR (1) | BR112012023147A2 (enExample) |
| ES (1) | ES2450123T3 (enExample) |
| WO (1) | WO2011117153A1 (enExample) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2012529544A (ja) | 2009-06-08 | 2012-11-22 | ビーエーエスエフ ソシエタス・ヨーロピア | セグメント化ポリアリーレンエーテルブロックコポリマー |
| WO2011107389A1 (de) * | 2010-03-05 | 2011-09-09 | Basf Se | Verbesserte blends aus polyarylenethern und polyarylensulfiden |
| US8952109B2 (en) | 2011-08-05 | 2015-02-10 | Basf Se | Process for preparing a block copolymer |
| CN104968710A (zh) | 2012-12-18 | 2015-10-07 | 索尔维特殊聚合物美国有限责任公司 | 由低氯芳香族聚砜制成的移动电子装置 |
| JP6193624B2 (ja) * | 2013-05-30 | 2017-09-06 | 帝人株式会社 | 樹脂組成物 |
| US10174199B2 (en) * | 2014-02-24 | 2019-01-08 | Teijin Limited | Resin composition |
| WO2016179772A1 (zh) * | 2015-05-11 | 2016-11-17 | 深圳华力兴新材料股份有限公司 | 一种超支化树脂增韧的pps工程塑料及其制备方法 |
| CN104845369B (zh) * | 2015-05-11 | 2018-01-26 | 深圳华力兴新材料股份有限公司 | 一种超支化树脂增韧的pps工程塑料及其制备方法 |
| US20190136056A1 (en) * | 2016-04-29 | 2019-05-09 | Solvay Specialty Polymers Usa, Llc | Compatibilized polymer compositions |
| CN106928710B (zh) * | 2017-04-24 | 2019-05-07 | 苏州纳磐新材料科技有限公司 | 聚苯硫醚复合材料及其制备方法 |
| CN111032783B (zh) * | 2017-08-28 | 2024-02-02 | 索尔维特殊聚合物美国有限责任公司 | 包含聚(芳基醚砜)、聚(芳基醚酮)、至少一种聚苯硫醚以及玻璃纤维的玻璃填充的聚合物组合物 |
| CN109593360B (zh) * | 2018-11-14 | 2020-07-24 | 苏州纳磐新材料科技有限公司 | 一种聚苯硫醚复合材料及其制备方法 |
| CN109777106B (zh) * | 2019-01-31 | 2021-08-31 | 珠海派锐尔新材料有限公司 | 一种聚芳醚砜/聚苯硫醚合金及其制备方法和应用 |
Family Cites Families (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2513188A (en) | 1948-09-10 | 1950-06-27 | Macallum Alexander Douglas | Mixed phenylene sulfide resins |
| BE613003A (fr) | 1961-01-27 | 1962-07-29 | Dow Chemical Co | Procédé de préparation de polysulfures d'arylène linéaires |
| US3354129A (en) | 1963-11-27 | 1967-11-21 | Phillips Petroleum Co | Production of polymers from aromatic compounds |
| US3699087A (en) | 1971-03-11 | 1972-10-17 | Phillips Petroleum Co | Heat treatment of aromatic sulfide polymers |
| US4645826A (en) | 1984-06-20 | 1987-02-24 | Kureha Kagaku Kogyo Kabushiki Kaisha | Process for production of high to ultra-high molecular weight linear polyarylenesulfides |
| DE3444339A1 (de) | 1984-12-05 | 1986-06-05 | Basf Ag, 6700 Ludwigshafen | Thermoplastische formmassen |
| EP0673973A1 (de) * | 1994-03-26 | 1995-09-27 | Basf Aktiengesellschaft | Mischungen auf der Basis von Polyarylenethern und Polyarylensulfiden |
| DE19702587A1 (de) * | 1997-01-24 | 1998-07-30 | Basf Ag | Thermoplastische Formmassen mit verbesserter Chemikalienresistenz |
| DE19702590A1 (de) * | 1997-01-24 | 1998-07-30 | Basf Ag | Thermoplastische Formmassen |
| DE19702588A1 (de) | 1997-01-24 | 1998-07-30 | Basf Ag | Thermoplastische Formmassen mit reduzierter Wasseraufnahme |
| DE19741467A1 (de) * | 1997-09-19 | 1999-03-25 | Basf Ag | Polyarylenether und Polyarylensulfide enthaltende Formmassen mit verbesserter Kerbschlagzähigkeit |
| DE19961040A1 (de) * | 1999-12-16 | 2001-06-21 | Basf Ag | Thermoplastische Formmassen mit verbessertem Verarbeitungsverhalten auf Basis von Polyarylenethersulfonen und Polyamiden |
| DE102004038979A1 (de) * | 2004-08-10 | 2006-02-23 | Basf Ag | Schlagzähmodifizierte Polyester mit hyperverzweigten Polyestern |
| DE102004049342A1 (de) * | 2004-10-08 | 2006-04-13 | Basf Ag | Fließfähige Thermoplaste mit halogenfreiem Flammschutz |
| DE102005033147A1 (de) * | 2005-07-13 | 2007-01-25 | Basf Ag | Fließfähige Thermoplaste mit Halogenflammschutz |
| US8073278B2 (en) | 2005-12-27 | 2011-12-06 | Nittoh Kogaku K.K. | Image processing device |
| JP5610769B2 (ja) | 2006-12-19 | 2014-10-22 | ビーエーエスエフ ソシエタス・ヨーロピアＢａｓｆ Ｓｅ | 優れた延性を有する熱可塑性成形材料 |
-
2011
- 2011-03-18 JP JP2013500443A patent/JP5791697B2/ja not_active Expired - Fee Related
- 2011-03-18 BR BR112012023147A patent/BR112012023147A2/pt not_active IP Right Cessation
- 2011-03-18 EP EP11708507.6A patent/EP2550335B1/de not_active Not-in-force
- 2011-03-18 KR KR1020127027451A patent/KR20130019396A/ko not_active Abandoned
- 2011-03-18 ES ES11708507.6T patent/ES2450123T3/es active Active
- 2011-03-18 CN CN201180015371.1A patent/CN102834464B/zh not_active Expired - Fee Related
- 2011-03-18 WO PCT/EP2011/054132 patent/WO2011117153A1/de not_active Ceased
Also Published As
| Publication number | Publication date |
|---|---|
| EP2550335B1 (de) | 2014-01-15 |
| CN102834464B (zh) | 2016-01-13 |
| JP5791697B2 (ja) | 2015-10-07 |
| CN102834464A (zh) | 2012-12-19 |
| KR20130019396A (ko) | 2013-02-26 |
| JP2013522429A (ja) | 2013-06-13 |
| WO2011117153A1 (de) | 2011-09-29 |
| EP2550335A1 (de) | 2013-01-30 |
| BR112012023147A2 (pt) | 2018-06-26 |
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