DE2556899C2 - Polymere Mischung - Google Patents
Polymere MischungInfo
- Publication number
- DE2556899C2 DE2556899C2 DE2556899A DE2556899A DE2556899C2 DE 2556899 C2 DE2556899 C2 DE 2556899C2 DE 2556899 A DE2556899 A DE 2556899A DE 2556899 A DE2556899 A DE 2556899A DE 2556899 C2 DE2556899 C2 DE 2556899C2
- Authority
- DE
- Germany
- Prior art keywords
- same
- air
- weight
- polybenzoxazole
- mixture
- 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.)
- Expired
Links
- 229920002959 polymer blend Polymers 0.000 title description 6
- 229920002577 polybenzoxazole Polymers 0.000 claims description 38
- 239000000203 mixture Substances 0.000 claims description 37
- 230000000087 stabilizing effect Effects 0.000 claims description 25
- 239000000654 additive Substances 0.000 claims description 21
- 230000000996 additive effect Effects 0.000 claims description 16
- MHDLAWFYLQAULB-UHFFFAOYSA-N anilinophosphonic acid Chemical class OP(O)(=O)NC1=CC=CC=C1 MHDLAWFYLQAULB-UHFFFAOYSA-N 0.000 claims description 2
- 239000003381 stabilizer Substances 0.000 description 19
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 16
- 238000012360 testing method Methods 0.000 description 13
- 230000032683 aging Effects 0.000 description 12
- 238000000034 method Methods 0.000 description 12
- 229920000642 polymer Polymers 0.000 description 12
- 150000003931 anilides Chemical class 0.000 description 9
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 8
- 239000000463 material Substances 0.000 description 8
- 238000007792 addition Methods 0.000 description 7
- 239000004642 Polyimide Substances 0.000 description 6
- 239000002253 acid Substances 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- 239000004744 fabric Substances 0.000 description 6
- 239000003365 glass fiber Substances 0.000 description 6
- 229920001721 polyimide Polymers 0.000 description 6
- 230000004580 weight loss Effects 0.000 description 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 5
- 229910052760 oxygen Inorganic materials 0.000 description 5
- 239000001301 oxygen Substances 0.000 description 5
- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 description 5
- ASMQGLCHMVWBQR-UHFFFAOYSA-N Diphenyl phosphate Chemical compound C=1C=CC=CC=1OP(=O)(O)OC1=CC=CC=C1 ASMQGLCHMVWBQR-UHFFFAOYSA-N 0.000 description 4
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 4
- 241000158147 Sator Species 0.000 description 4
- 229940051881 anilide analgesics and antipyretics Drugs 0.000 description 4
- 230000006378 damage Effects 0.000 description 4
- 150000002148 esters Chemical class 0.000 description 4
- 239000000835 fiber Substances 0.000 description 4
- 239000011152 fibreglass Substances 0.000 description 4
- 239000011521 glass Substances 0.000 description 4
- 229920003023 plastic Polymers 0.000 description 4
- 239000004033 plastic Substances 0.000 description 4
- 239000002990 reinforced plastic Substances 0.000 description 4
- AAQFSZFQCXLMNT-ACMTZBLWSA-N (3s)-3-amino-4-[[(2s)-1-methoxy-1-oxo-3-phenylpropan-2-yl]amino]-4-oxobutanoic acid;hydrochloride Chemical compound Cl.OC(=O)C[C@H](N)C(=O)N[C@H](C(=O)OC)CC1=CC=CC=C1 AAQFSZFQCXLMNT-ACMTZBLWSA-N 0.000 description 3
- DZKXDEWNLDOXQH-UHFFFAOYSA-N 1,3,5,2,4,6-triazatriphosphinine Chemical compound N1=PN=PN=P1 DZKXDEWNLDOXQH-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- DILJSNXGQARQSW-UHFFFAOYSA-N OP(O)(O)C1=CC=CC=C1 Chemical compound OP(O)(O)C1=CC=CC=C1 DILJSNXGQARQSW-UHFFFAOYSA-N 0.000 description 3
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 3
- FDQSRULYDNDXQB-UHFFFAOYSA-N benzene-1,3-dicarbonyl chloride Chemical compound ClC(=O)C1=CC=CC(C(Cl)=O)=C1 FDQSRULYDNDXQB-UHFFFAOYSA-N 0.000 description 3
- 238000010276 construction Methods 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000012778 molding material Substances 0.000 description 3
- GKTNLYAAZKKMTQ-UHFFFAOYSA-N n-[bis(dimethylamino)phosphinimyl]-n-methylmethanamine Chemical class CN(C)P(=N)(N(C)C)N(C)C GKTNLYAAZKKMTQ-UHFFFAOYSA-N 0.000 description 3
- 229910052698 phosphorus Inorganic materials 0.000 description 3
- 239000011574 phosphorus Substances 0.000 description 3
- -1 3-naphthylphosphorous acid dianilide Chemical compound 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- CMPQUABWPXYYSH-UHFFFAOYSA-N phenyl phosphate Chemical compound OP(O)(=O)OC1=CC=CC=C1 CMPQUABWPXYYSH-UHFFFAOYSA-N 0.000 description 2
- 150000003018 phosphorus compounds Chemical class 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- VYDHXSBCDVWTAV-UHFFFAOYSA-N (n-(2-phenylphenyl)anilino)phosphonic acid Chemical compound C=1C=CC=C(C=2C=CC=CC=2)C=1N(P(O)(=O)O)C1=CC=CC=C1 VYDHXSBCDVWTAV-UHFFFAOYSA-N 0.000 description 1
- HLBLWEWZXPIGSM-UHFFFAOYSA-N 4-Aminophenyl ether Chemical compound C1=CC(N)=CC=C1OC1=CC=C(N)C=C1 HLBLWEWZXPIGSM-UHFFFAOYSA-N 0.000 description 1
- 241001387976 Pera Species 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- KBJIFQCCHDKZMQ-UHFFFAOYSA-N anilino-(N-phenylanilino)phosphinic acid Chemical compound C1(=CC=CC=C1)N(C1=CC=CC=C1)P(O)(=O)NC1=CC=CC=C1 KBJIFQCCHDKZMQ-UHFFFAOYSA-N 0.000 description 1
- JXRNXOOUAJKBCK-UHFFFAOYSA-N anilinophosphonous acid Chemical class OP(O)NC1=CC=CC=C1 JXRNXOOUAJKBCK-UHFFFAOYSA-N 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- JJWKPURADFRFRB-UHFFFAOYSA-N carbonyl sulfide Chemical compound O=C=S JJWKPURADFRFRB-UHFFFAOYSA-N 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000004870 electrical engineering Methods 0.000 description 1
- ZJXZSIYSNXKHEA-UHFFFAOYSA-N ethyl dihydrogen phosphate Chemical compound CCOP(O)(O)=O ZJXZSIYSNXKHEA-UHFFFAOYSA-N 0.000 description 1
- 210000003734 kidney Anatomy 0.000 description 1
- 238000009533 lab test Methods 0.000 description 1
- 238000011089 mechanical engineering Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920002480 polybenzimidazole Polymers 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- STCOOQWBFONSKY-UHFFFAOYSA-N tributyl phosphate Chemical compound CCCCOP(=O)(OCCCC)OCCCC STCOOQWBFONSKY-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
- C08K5/00—Use of organic ingredients
- C08K5/49—Phosphorus-containing compounds
-
- 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
- C08K5/00—Use of organic ingredients
- C08K5/49—Phosphorus-containing compounds
- C08K5/5399—Phosphorus bound to nitrogen
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)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SU742096420A SU692261A1 (ru) | 1974-12-19 | 1974-12-19 | Полимерна композици |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE2556899A1 DE2556899A1 (de) | 1976-07-01 |
| DE2556899C2 true DE2556899C2 (de) | 1981-12-17 |
Family
ID=20607378
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE2556899A Expired DE2556899C2 (de) | 1974-12-19 | 1975-12-17 | Polymere Mischung |
Country Status (7)
| Country | Link |
|---|---|
| JP (1) | JPS5634181B2 (esLanguage) |
| AT (1) | AT353485B (esLanguage) |
| DE (1) | DE2556899C2 (esLanguage) |
| FR (1) | FR2295076A1 (esLanguage) |
| GB (1) | GB1479418A (esLanguage) |
| IT (1) | IT1060396B (esLanguage) |
| SU (1) | SU692261A1 (esLanguage) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2002501018A (ja) | 1998-01-26 | 2002-01-15 | マイトコー | ミトコンドリア関連疾患を処置するためのミトコンドリア保護剤 |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3359233A (en) * | 1964-06-18 | 1967-12-19 | Stauffer Chemical Co | Poly-gamma-olefin compositions containing n, n, n', n'-tetralkylphosphorodiamidothioic acid and esters thereof |
| US3781385A (en) * | 1971-04-05 | 1973-12-25 | Uniroyal Inc | Polymeric phenolic phosphorous acid ester amides |
| CH574967A5 (esLanguage) * | 1973-03-27 | 1976-04-30 | Ciba Geigy Ag | |
| DK385574A (esLanguage) * | 1973-08-10 | 1975-04-21 | Ciba Geigy Ag | |
| DE2459685A1 (de) * | 1973-12-22 | 1975-06-26 | Kuraray Co | Flammfeste, thermoplastische polymerisatmasse |
-
1974
- 1974-12-19 SU SU742096420A patent/SU692261A1/ru active
-
1975
- 1975-12-17 FR FR7538676A patent/FR2295076A1/fr active Granted
- 1975-12-17 DE DE2556899A patent/DE2556899C2/de not_active Expired
- 1975-12-18 IT IT30473/75A patent/IT1060396B/it active
- 1975-12-19 GB GB52153/75A patent/GB1479418A/en not_active Expired
- 1975-12-19 AT AT969375A patent/AT353485B/de not_active IP Right Cessation
- 1975-12-19 JP JP15069575A patent/JPS5634181B2/ja not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| DE2556899A1 (de) | 1976-07-01 |
| JPS5634181B2 (esLanguage) | 1981-08-08 |
| FR2295076A1 (fr) | 1976-07-16 |
| JPS5276365A (esLanguage) | 1977-06-27 |
| IT1060396B (it) | 1982-07-10 |
| AT353485B (de) | 1979-11-12 |
| FR2295076B1 (esLanguage) | 1978-05-19 |
| ATA969375A (de) | 1979-04-15 |
| SU692261A1 (ru) | 1984-06-15 |
| GB1479418A (en) | 1977-07-13 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| OD | Request for examination | ||
| D2 | Grant after examination | ||
| 8328 | Change in the person/name/address of the agent |
Free format text: VON FUENER, A., DIPL.-CHEM. DR.RER.NAT. EBBINGHAUS, D., DIPL.-ING., PAT.-ANW., 8000 MUENCHEN |
|
| 8339 | Ceased/non-payment of the annual fee |