JP2009529074A - 高い結晶性を有する部分芳香族コポリアミド - Google Patents
高い結晶性を有する部分芳香族コポリアミド Download PDFInfo
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- JP2009529074A JP2009529074A JP2008557719A JP2008557719A JP2009529074A JP 2009529074 A JP2009529074 A JP 2009529074A JP 2008557719 A JP2008557719 A JP 2008557719A JP 2008557719 A JP2008557719 A JP 2008557719A JP 2009529074 A JP2009529074 A JP 2009529074A
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- GHPGOEFPKIHBNM-UHFFFAOYSA-N antimony(3+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[Sb+3].[Sb+3] GHPGOEFPKIHBNM-UHFFFAOYSA-N 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000004760 aramid Substances 0.000 description 1
- 229920006231 aramid fiber Polymers 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000012965 benzophenone Chemical class 0.000 description 1
- 150000008366 benzophenones Chemical class 0.000 description 1
- 150000001565 benzotriazoles Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- ZPOLOEWJWXZUSP-AATRIKPKSA-N bis(prop-2-enyl) (e)-but-2-enedioate Chemical compound C=CCOC(=O)\C=C\C(=O)OCC=C ZPOLOEWJWXZUSP-AATRIKPKSA-N 0.000 description 1
- ZPOLOEWJWXZUSP-WAYWQWQTSA-N bis(prop-2-enyl) (z)-but-2-enedioate Chemical compound C=CCOC(=O)\C=C/C(=O)OCC=C ZPOLOEWJWXZUSP-WAYWQWQTSA-N 0.000 description 1
- QUDWYFHPNIMBFC-UHFFFAOYSA-N bis(prop-2-enyl) benzene-1,2-dicarboxylate Chemical compound C=CCOC(=O)C1=CC=CC=C1C(=O)OCC=C QUDWYFHPNIMBFC-UHFFFAOYSA-N 0.000 description 1
- RELIZYGLMJFIOW-UHFFFAOYSA-N butyl prop-2-enoate;oxiran-2-ylmethyl prop-2-enoate Chemical compound CCCCOC(=O)C=C.C=CC(=O)OCC1CO1 RELIZYGLMJFIOW-UHFFFAOYSA-N 0.000 description 1
- 229910052793 cadmium Inorganic materials 0.000 description 1
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 235000012241 calcium silicate Nutrition 0.000 description 1
- 239000004917 carbon fiber Substances 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- YACLQRRMGMJLJV-UHFFFAOYSA-N chloroprene Chemical compound ClC(=C)C=C YACLQRRMGMJLJV-UHFFFAOYSA-N 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 229910000423 chromium oxide Inorganic materials 0.000 description 1
- IVMYJDGYRUAWML-UHFFFAOYSA-N cobalt(ii) oxide Chemical compound [Co]=O IVMYJDGYRUAWML-UHFFFAOYSA-N 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 150000001990 dicarboxylic acid derivatives Chemical class 0.000 description 1
- 125000001142 dicarboxylic acid group Chemical group 0.000 description 1
- ISRJTGUYHVPAOR-UHFFFAOYSA-N dihydrodicyclopentadienyl acrylate Chemical compound C1CC2C3C(OC(=O)C=C)C=CC3C1C2 ISRJTGUYHVPAOR-UHFFFAOYSA-N 0.000 description 1
- VVYDVQWJZWRVPE-UHFFFAOYSA-L dimethyltin(2+);diiodide Chemical compound C[Sn](C)(I)I VVYDVQWJZWRVPE-UHFFFAOYSA-L 0.000 description 1
- NJLLQSBAHIKGKF-UHFFFAOYSA-N dipotassium dioxido(oxo)titanium Chemical compound [K+].[K+].[O-][Ti]([O-])=O NJLLQSBAHIKGKF-UHFFFAOYSA-N 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 238000007720 emulsion polymerization reaction Methods 0.000 description 1
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 229920001038 ethylene copolymer Polymers 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 239000010433 feldspar Substances 0.000 description 1
- 239000012634 fragment Substances 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 239000006232 furnace black Substances 0.000 description 1
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- RBTKNAXYKSUFRK-UHFFFAOYSA-N heliogen blue Chemical compound [Cu].[N-]1C2=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=NC([N-]1)=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=N2 RBTKNAXYKSUFRK-UHFFFAOYSA-N 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- WTFXARWRTYJXII-UHFFFAOYSA-N iron(2+);iron(3+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[O-2].[Fe+2].[Fe+3].[Fe+3] WTFXARWRTYJXII-UHFFFAOYSA-N 0.000 description 1
- SZVJSHCCFOBDDC-UHFFFAOYSA-N iron(II,III) oxide Inorganic materials O=[Fe]O[Fe]O[Fe]=O SZVJSHCCFOBDDC-UHFFFAOYSA-N 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 150000002531 isophthalic acids Chemical class 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 239000011133 lead Substances 0.000 description 1
- 239000003446 ligand Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 150000004668 long chain fatty acids Chemical class 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- 230000001404 mediated effect Effects 0.000 description 1
- 229910001507 metal halide Inorganic materials 0.000 description 1
- 150000005309 metal halides Chemical class 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 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
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- QYZLKGVUSQXAMU-UHFFFAOYSA-N penta-1,4-diene Chemical compound C=CCC=C QYZLKGVUSQXAMU-UHFFFAOYSA-N 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 239000004597 plastic additive Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 238000012643 polycondensation polymerization Methods 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- FBCQUCJYYPMKRO-UHFFFAOYSA-N prop-2-enyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC=C FBCQUCJYYPMKRO-UHFFFAOYSA-N 0.000 description 1
- QTECDUFMBMSHKR-UHFFFAOYSA-N prop-2-enyl prop-2-enoate Chemical compound C=CCOC(=O)C=C QTECDUFMBMSHKR-UHFFFAOYSA-N 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- PNXMTCDJUBJHQJ-UHFFFAOYSA-N propyl prop-2-enoate Chemical compound CCCOC(=O)C=C PNXMTCDJUBJHQJ-UHFFFAOYSA-N 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000002787 reinforcement Effects 0.000 description 1
- 239000012744 reinforcing agent Substances 0.000 description 1
- 150000003873 salicylate salts Chemical class 0.000 description 1
- 229920002379 silicone rubber Polymers 0.000 description 1
- 238000004513 sizing Methods 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011029 spinel Substances 0.000 description 1
- 229910052596 spinel Inorganic materials 0.000 description 1
- 229940037312 stearamide Drugs 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 238000010557 suspension polymerization reaction Methods 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 150000003504 terephthalic acids Chemical class 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
- ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 1
- 150000003509 tertiary alcohols Chemical class 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 238000002076 thermal analysis method Methods 0.000 description 1
- 239000003017 thermal stabilizer Substances 0.000 description 1
- 239000012815 thermoplastic material Substances 0.000 description 1
- 238000009757 thermoplastic moulding Methods 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 239000011135 tin Substances 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 150000003609 titanium compounds Chemical class 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 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
- DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical compound [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 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
- C08G69/00—Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
- C08G69/02—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids
- C08G69/26—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids derived from polyamines and polycarboxylic acids
- C08G69/265—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids derived from polyamines and polycarboxylic acids from at least two different diamines or at least two different dicarboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L77/00—Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
- C08L77/06—Polyamides derived from polyamines and polycarboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2203/00—Foams characterized by the expanding agent
- C08J2203/22—Expandable microspheres, e.g. Expancel®
-
- 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
- C08K7/00—Use of ingredients characterised by shape
- C08K7/02—Fibres or whiskers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2203/00—Applications
- C08L2203/12—Applications used for fibers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; 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
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/16—Ethene-propene or ethene-propene-diene copolymers
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Polyamides (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP06110815 | 2006-03-08 | ||
| PCT/EP2007/051865 WO2007101809A2 (de) | 2006-03-08 | 2007-02-28 | Teilaromatische copolyamide mit hoher kristallinität |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2009529074A true JP2009529074A (ja) | 2009-08-13 |
| JP2009529074A5 JP2009529074A5 (OSRAM) | 2012-10-11 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2008557719A Ceased JP2009529074A (ja) | 2006-03-08 | 2007-02-28 | 高い結晶性を有する部分芳香族コポリアミド |
Country Status (21)
| Country | Link |
|---|---|
| US (1) | US20090012229A1 (OSRAM) |
| EP (1) | EP1994075B1 (OSRAM) |
| JP (1) | JP2009529074A (OSRAM) |
| KR (1) | KR20080100288A (OSRAM) |
| CN (1) | CN101395203B (OSRAM) |
| AT (1) | ATE441684T1 (OSRAM) |
| AU (1) | AU2007222453A1 (OSRAM) |
| BR (1) | BRPI0708591A2 (OSRAM) |
| CA (1) | CA2642925A1 (OSRAM) |
| DE (1) | DE502007001447D1 (OSRAM) |
| DK (1) | DK1994075T3 (OSRAM) |
| ES (1) | ES2329309T3 (OSRAM) |
| IL (1) | IL193457A0 (OSRAM) |
| MX (1) | MX2008010730A (OSRAM) |
| MY (1) | MY144115A (OSRAM) |
| NO (1) | NO20083719L (OSRAM) |
| PL (1) | PL1994075T3 (OSRAM) |
| RU (1) | RU2008139636A (OSRAM) |
| SI (1) | SI1994075T1 (OSRAM) |
| WO (1) | WO2007101809A2 (OSRAM) |
| ZA (1) | ZA200808488B (OSRAM) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2012515805A (ja) * | 2009-01-21 | 2012-07-12 | ディーエスエム アイピー アセッツ ビー．ブイ． | プラスチック容器および導管 |
| JP2016521791A (ja) * | 2013-06-12 | 2016-07-25 | ビーエーエスエフ ソシエタス・ヨーロピアＢａｓｆ Ｓｅ | 高いガラス転移温度および高い結晶化度を有する部分芳香族コポリアミド |
Families Citing this family (65)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8309221B2 (en) * | 2007-10-01 | 2012-11-13 | Jay Plaehn | Reinforced foam panel |
| FR2947556B1 (fr) * | 2009-07-03 | 2011-07-15 | Rhodia Operations | Composition polyamide modifiee |
| PH12012500717A1 (en) | 2009-10-27 | 2012-10-29 | Basf Se | Polyamide resistant to heat aging |
| JP5496351B2 (ja) | 2009-10-27 | 2014-05-21 | ビーエーエスエフ ソシエタス・ヨーロピア | 難燃剤を有する耐熱老化性ポリアミド |
| WO2011069942A1 (de) | 2009-12-08 | 2011-06-16 | Basf Se | Teilaromatische copolyamidformmassen auf der basis von octamethylendiamin |
| WO2011069984A1 (de) | 2009-12-09 | 2011-06-16 | Basf Se | Teilaromatische, teilkristalline copolyamide |
| DE102010062886A1 (de) | 2009-12-16 | 2011-06-22 | Basf Se, 67063 | Polyarylenethersulfone als Schlagzähmodifier |
| EP2528973A2 (en) * | 2010-01-29 | 2012-12-05 | E.I. Du Pont De Nemours And Company | Polyamide compositions with improved salt resistance and heat stability |
| KR101864682B1 (ko) | 2010-03-09 | 2018-06-07 | 바스프 에스이 | 열노화에 내성인 폴리아미드 |
| US8466221B2 (en) * | 2010-03-09 | 2013-06-18 | Basf Se | Polyamides that resist heat-aging |
| US8563680B2 (en) | 2010-06-15 | 2013-10-22 | Basf Se | Heat-aging-resistant polyamides |
| EP2582759B1 (de) | 2010-06-15 | 2019-04-17 | Basf Se | Wärmealterungsbeständige polyamide |
| DE102010023770A1 (de) | 2010-06-15 | 2011-12-15 | Basf Se | Glühdrahtbeständige Formmassen |
| EP2410020B1 (de) * | 2010-07-23 | 2013-01-30 | Ems-Patent Ag | Teilaromatische Polyamid-Formmassen und deren Verwendungen |
| EP2415827A1 (de) | 2010-08-04 | 2012-02-08 | Basf Se | Flammgeschützte Polyamide mit Schichtsilikaten |
| WO2012062594A1 (de) | 2010-11-11 | 2012-05-18 | Basf Se | Wärmealterungsbeständige polyamide |
| WO2012080403A1 (de) | 2010-12-16 | 2012-06-21 | Basf Se | Glühdrahtbeständige polyamide |
| US8575295B2 (en) | 2010-12-16 | 2013-11-05 | Basf Se | Glow-wire resistant polyamides |
| US8629220B2 (en) | 2011-01-18 | 2014-01-14 | Basf Se | Hydrolysis-resistant polyamides |
| WO2012098063A1 (de) | 2011-01-18 | 2012-07-26 | Basf Se | Hydrolysestabile polyamide |
| US8629206B2 (en) | 2011-01-20 | 2014-01-14 | Basf Se | Flame-retardant thermoplastic molding composition |
| WO2012143316A1 (de) | 2011-04-21 | 2012-10-26 | Basf Se | Vorrichtung zur befestigung von wärmeträgerleitungen an einem behälter |
| JP2014517093A (ja) | 2011-04-28 | 2014-07-17 | ビーエーエスエフ ソシエタス・ヨーロピア | 難燃性成形材料 |
| US8653168B2 (en) | 2011-05-10 | 2014-02-18 | Basf Se | Flame-retardant thermoplastic molding composition |
| US8883904B2 (en) | 2011-09-15 | 2014-11-11 | Basf Se | Mixtures of silver and zinc oxide as stabilizer for flame-retardant polyamides |
| EP2756033B1 (de) | 2011-09-15 | 2015-06-24 | Basf Se | Silber-zinkoxid-mischungen als stabilisator für flammgeschützte polyamide enthaltend roten phosphor |
| EP2573138A1 (de) | 2011-09-21 | 2013-03-27 | Basf Se | Polyamid-Formmassen |
| WO2013075982A1 (de) | 2011-11-25 | 2013-05-30 | Basf Se | Blasformbare polyamidformmassen |
| WO2013083508A1 (de) | 2011-12-07 | 2013-06-13 | Basf Se | Flammgeschützte polyamide mit flüssigkristallinen polyestern |
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- 2007-02-28 EP EP07712354A patent/EP1994075B1/de not_active Not-in-force
- 2007-02-28 RU RU2008139636/04A patent/RU2008139636A/ru not_active Application Discontinuation
- 2007-02-28 MX MX2008010730A patent/MX2008010730A/es not_active Application Discontinuation
- 2007-02-28 US US12/282,059 patent/US20090012229A1/en not_active Abandoned
- 2007-02-28 PL PL07712354T patent/PL1994075T3/pl unknown
- 2007-02-28 SI SI200730100T patent/SI1994075T1/sl unknown
- 2007-02-28 CN CN2007800080413A patent/CN101395203B/zh not_active Expired - Fee Related
- 2007-02-28 BR BRPI0708591-5A patent/BRPI0708591A2/pt not_active IP Right Cessation
- 2007-02-28 ES ES07712354T patent/ES2329309T3/es active Active
- 2007-02-28 WO PCT/EP2007/051865 patent/WO2007101809A2/de not_active Ceased
- 2007-02-28 JP JP2008557719A patent/JP2009529074A/ja not_active Ceased
- 2007-02-28 KR KR1020087024458A patent/KR20080100288A/ko not_active Ceased
- 2007-02-28 CA CA002642925A patent/CA2642925A1/en not_active Abandoned
- 2007-02-28 AU AU2007222453A patent/AU2007222453A1/en not_active Abandoned
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2008
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- 2008-08-29 MY MYPI20083353A patent/MY144115A/en unknown
- 2008-08-29 NO NO20083719A patent/NO20083719L/no not_active Application Discontinuation
- 2008-10-06 ZA ZA200808488A patent/ZA200808488B/xx unknown
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| JP2012515805A (ja) * | 2009-01-21 | 2012-07-12 | ディーエスエム アイピー アセッツ ビー．ブイ． | プラスチック容器および導管 |
| JP2016521791A (ja) * | 2013-06-12 | 2016-07-25 | ビーエーエスエフ ソシエタス・ヨーロピアＢａｓｆ Ｓｅ | 高いガラス転移温度および高い結晶化度を有する部分芳香族コポリアミド |
Also Published As
| Publication number | Publication date |
|---|---|
| NO20083719L (no) | 2008-10-06 |
| MY144115A (en) | 2011-08-15 |
| WO2007101809A2 (de) | 2007-09-13 |
| US20090012229A1 (en) | 2009-01-08 |
| IL193457A0 (en) | 2009-08-03 |
| EP1994075A2 (de) | 2008-11-26 |
| ATE441684T1 (de) | 2009-09-15 |
| RU2008139636A (ru) | 2010-04-20 |
| DK1994075T3 (da) | 2009-12-07 |
| SI1994075T1 (sl) | 2010-01-29 |
| WO2007101809A3 (de) | 2007-11-29 |
| EP1994075B1 (de) | 2009-09-02 |
| AU2007222453A1 (en) | 2007-09-13 |
| CA2642925A1 (en) | 2007-09-13 |
| BRPI0708591A2 (pt) | 2011-06-07 |
| PL1994075T3 (pl) | 2010-02-26 |
| MX2008010730A (es) | 2008-09-01 |
| KR20080100288A (ko) | 2008-11-14 |
| ZA200808488B (en) | 2009-12-30 |
| CN101395203B (zh) | 2011-05-04 |
| CN101395203A (zh) | 2009-03-25 |
| ES2329309T3 (es) | 2009-11-24 |
| DE502007001447D1 (de) | 2009-10-15 |
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