DE19906018A1 - Polymerblends aus funktionalisierten Kohlenmonoxidcopolymeren und Polyamiden - Google Patents

Polymerblends aus funktionalisierten Kohlenmonoxidcopolymeren und Polyamiden

Info

Publication number: DE19906018A1
Authority: DE; Germany
Prior art keywords: weight; carbon monoxide; acid; component; polymer blends
Prior art date: 1999-02-16
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 Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Withdrawn

Application number

DE1999106018

Other languages

German (de)

English (en)

Inventor

Martin Weber

Klaus Muehlbach

Joachim Queisser

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

BASF SE

Original Assignee

BASF SE

Priority date (The priority date 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 date listed.)

1999-02-16

Filing date

1999-02-16

Publication date

2000-08-17

1999-02-16 Application filed by BASF SE filed Critical BASF SE

1999-02-16 Priority to DE1999106018 priority Critical patent/DE19906018A1/de

2000-02-05 Priority to PCT/EP2000/000912 priority patent/WO2000049088A1/fr

2000-02-05 Priority to AU29067/00A priority patent/AU2906700A/en

2000-08-17 Publication of DE19906018A1 publication Critical patent/DE19906018A1/de

Status Withdrawn legal-status Critical Current

Links

229910002091 carbon monoxide Inorganic materials 0.000 title claims abstract description 89
229920001577 copolymer Polymers 0.000 title claims abstract description 88
229920002647 polyamide Polymers 0.000 title claims abstract description 43
239000004952 Polyamide Substances 0.000 title claims abstract description 42
229920002959 polymer blend Polymers 0.000 title claims abstract description 29
238000004519 manufacturing process Methods 0.000 title claims abstract description 26
239000000654 additive Substances 0.000 title claims abstract description 8
239000000203 mixture Substances 0.000 claims abstract description 63
229920001971 elastomer Polymers 0.000 claims abstract description 40
239000005060 rubber Substances 0.000 claims abstract description 28
238000000034 method Methods 0.000 claims abstract description 17
230000008569 process Effects 0.000 claims abstract description 10
239000000945 filler Substances 0.000 claims abstract description 5
229940105305 carbon monoxide Drugs 0.000 claims description 87
150000001875 compounds Chemical class 0.000 claims description 28
UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 claims description 23
125000000524 functional group Chemical group 0.000 claims description 17
238000000465 moulding Methods 0.000 claims description 13
ACZGCWSMSTYWDQ-UHFFFAOYSA-N 3h-1-benzofuran-2-one Chemical class C1=CC=C2OC(=O)CC2=C1 ACZGCWSMSTYWDQ-UHFFFAOYSA-N 0.000 claims description 8
239000000835 fiber Substances 0.000 claims description 8
239000003963 antioxidant agent Substances 0.000 claims description 7
229910019142 PO4 Inorganic materials 0.000 claims description 6
235000021317 phosphate Nutrition 0.000 claims description 6
150000003013 phosphoric acid derivatives Chemical class 0.000 claims description 6
239000006078 metal deactivator Substances 0.000 claims description 5
239000006096 absorbing agent Substances 0.000 claims description 4
150000004649 carbonic acid derivatives Chemical class 0.000 claims description 4
239000012779 reinforcing material Substances 0.000 claims description 4
239000011888 foil Substances 0.000 claims description 3
238000002360 preparation method Methods 0.000 claims description 3
150000003467 sulfuric acid derivatives Chemical class 0.000 claims description 3
229910052816 inorganic phosphate Inorganic materials 0.000 claims 1
238000013329 compounding Methods 0.000 abstract 1
239000012744 reinforcing agent Substances 0.000 abstract 1
-1 vinyl aromatic compounds Chemical class 0.000 description 67
239000000178 monomer Substances 0.000 description 54
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 38
229920000642 polymer Polymers 0.000 description 24
KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 20
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 20
150000001993 dienes Chemical class 0.000 description 20
QQONPFPTGQHPMA-UHFFFAOYSA-N Propene Chemical compound CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 19
125000004432 carbon atom Chemical group C* 0.000 description 19
NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 19
239000002253 acid Substances 0.000 description 17
150000003254 radicals Chemical class 0.000 description 17
JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 16
229920002554 vinyl polymer Polymers 0.000 description 16
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 15
OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 15
229920001400 block copolymer Polymers 0.000 description 15
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 15
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 14
229910052739 hydrogen Inorganic materials 0.000 description 14
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 14
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 13
VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 12
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 12
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 12
RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 12
KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 12
238000006243 chemical reaction Methods 0.000 description 12
239000000806 elastomer Substances 0.000 description 12
239000001257 hydrogen Substances 0.000 description 12
150000001991 dicarboxylic acids Chemical class 0.000 description 11
150000002148 esters Chemical class 0.000 description 11
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid group Chemical group C(\C=C/C(=O)O)(=O)O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 11
239000012071 phase Substances 0.000 description 11
239000000243 solution Substances 0.000 description 11
239000003381 stabilizer Substances 0.000 description 11
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 10
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 10
239000003365 glass fiber Substances 0.000 description 10
150000003951 lactams Chemical class 0.000 description 10
239000011976 maleic acid Substances 0.000 description 10
239000000155 melt Substances 0.000 description 10
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 10
229910052757 nitrogen Inorganic materials 0.000 description 10
239000000049 pigment Substances 0.000 description 10
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 9
150000007513 acids Chemical class 0.000 description 9
125000003118 aryl group Chemical group 0.000 description 9
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 9
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 9
KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 8
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 8
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 8
238000007792 addition Methods 0.000 description 8
238000002844 melting Methods 0.000 description 8
230000008018 melting Effects 0.000 description 8
239000000126 substance Substances 0.000 description 8
229920002943 EPDM rubber Polymers 0.000 description 7
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 7
239000001361 adipic acid Substances 0.000 description 7
235000011037 adipic acid Nutrition 0.000 description 7
230000000875 corresponding effect Effects 0.000 description 7
238000004132 cross linking Methods 0.000 description 7
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 7
239000003999 initiator Substances 0.000 description 7
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical group O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 7
238000002156 mixing Methods 0.000 description 7
150000002894 organic compounds Chemical class 0.000 description 7
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 6
CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 6
229910052799 carbon Inorganic materials 0.000 description 6
238000009833 condensation Methods 0.000 description 6
230000009477 glass transition Effects 0.000 description 6
QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 6
238000006116 polymerization reaction Methods 0.000 description 6
229920000098 polyolefin Polymers 0.000 description 6
KIDHWZJUCRJVML-UHFFFAOYSA-N putrescine Chemical compound NCCCCN KIDHWZJUCRJVML-UHFFFAOYSA-N 0.000 description 6
229920006024 semi-aromatic copolyamide Polymers 0.000 description 6
229920001897 terpolymer Polymers 0.000 description 6
QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 6
239000004711 α-olefin Substances 0.000 description 6
HCILJBJJZALOAL-UHFFFAOYSA-N 3-(3,5-ditert-butyl-4-hydroxyphenyl)-n'-[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyl]propanehydrazide Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)NNC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 HCILJBJJZALOAL-UHFFFAOYSA-N 0.000 description 5
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 5
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 5
239000005977 Ethylene Substances 0.000 description 5
239000004609 Impact Modifier Substances 0.000 description 5
OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 5
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
125000005396 acrylic acid ester group Chemical group 0.000 description 5
125000001931 aliphatic group Chemical group 0.000 description 5
150000008064 anhydrides Chemical class 0.000 description 5
235000006708 antioxidants Nutrition 0.000 description 5
239000001506 calcium phosphate Substances 0.000 description 5
229910000389 calcium phosphate Inorganic materials 0.000 description 5
235000011010 calcium phosphates Nutrition 0.000 description 5
150000001732 carboxylic acid derivatives Chemical group 0.000 description 5
239000003054 catalyst Substances 0.000 description 5
230000005494 condensation Effects 0.000 description 5
150000004985 diamines Chemical class 0.000 description 5
HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 description 5
229910052751 metal Inorganic materials 0.000 description 5
239000002184 metal Substances 0.000 description 5
RPQRDASANLAFCM-UHFFFAOYSA-N oxiran-2-ylmethyl prop-2-enoate Chemical compound C=CC(=O)OCC1CO1 RPQRDASANLAFCM-UHFFFAOYSA-N 0.000 description 5
YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 description 5
229910052698 phosphorus Inorganic materials 0.000 description 5
239000011574 phosphorus Substances 0.000 description 5
239000007858 starting material Substances 0.000 description 5
229920001169 thermoplastic Polymers 0.000 description 5
239000004416 thermosoftening plastic Substances 0.000 description 5
229920001567 vinyl ester resin Polymers 0.000 description 5
125000000008 (C1-C10) alkyl group Chemical group 0.000 description 4
MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 4
ZGEGCLOFRBLKSE-UHFFFAOYSA-N 1-Heptene Chemical compound CCCCCC=C ZGEGCLOFRBLKSE-UHFFFAOYSA-N 0.000 description 4
LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 4
239000004593 Epoxy Substances 0.000 description 4
OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 4
BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 4
229920002292 Nylon 6 Polymers 0.000 description 4
GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 4
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
125000000217 alkyl group Chemical group 0.000 description 4
230000001588 bifunctional effect Effects 0.000 description 4
VHRGRCVQAFMJIZ-UHFFFAOYSA-N cadaverine Chemical compound NCCCCCN VHRGRCVQAFMJIZ-UHFFFAOYSA-N 0.000 description 4
ZSWFCLXCOIISFI-UHFFFAOYSA-N cyclopentadiene Chemical compound C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 description 4
TVIDDXQYHWJXFK-UHFFFAOYSA-N dodecanedioic acid Chemical compound OC(=O)CCCCCCCCCCC(O)=O TVIDDXQYHWJXFK-UHFFFAOYSA-N 0.000 description 4
239000001530 fumaric acid Substances 0.000 description 4
125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 4
VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 description 4
229920000578 graft copolymer Polymers 0.000 description 4
239000003446 ligand Substances 0.000 description 4
239000011159 matrix material Substances 0.000 description 4
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 4
125000001624 naphthyl group Chemical group 0.000 description 4
BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 4
GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 4
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
150000003839 salts Chemical class 0.000 description 4
CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 4
239000007790 solid phase Substances 0.000 description 4
TYFQFVWCELRYAO-UHFFFAOYSA-N suberic acid Chemical compound OC(=O)CCCCCCC(O)=O TYFQFVWCELRYAO-UHFFFAOYSA-N 0.000 description 4
JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 4
125000004178 (C1-C4) alkyl group Chemical group 0.000 description 3
HECLRDQVFMWTQS-RGOKHQFPSA-N 1755-01-7 Chemical compound C1[C@H]2[C@@H]3CC=C[C@@H]3[C@@H]1C=C2 HECLRDQVFMWTQS-RGOKHQFPSA-N 0.000 description 3
JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 3
GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 3
IMSODMZESSGVBE-UHFFFAOYSA-N 2-Oxazoline Chemical compound C1CN=CO1 IMSODMZESSGVBE-UHFFFAOYSA-N 0.000 description 3
BCHZICNRHXRCHY-UHFFFAOYSA-N 2h-oxazine Chemical group N1OC=CC=C1 BCHZICNRHXRCHY-UHFFFAOYSA-N 0.000 description 3
239000004953 Aliphatic polyamide Substances 0.000 description 3
KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical class NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 3
229920008712 Copo Polymers 0.000 description 3
JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 3
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 3
GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 description 3
150000001252 acrylic acid derivatives Chemical class 0.000 description 3
150000001298 alcohols Chemical class 0.000 description 3
229920003231 aliphatic polyamide Polymers 0.000 description 3
229910052784 alkaline earth metal Inorganic materials 0.000 description 3
XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 3
150000001408 amides Chemical class 0.000 description 3
238000010539 anionic addition polymerization reaction Methods 0.000 description 3
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239000011575 calcium Substances 0.000 description 3
239000003795 chemical substances by application Substances 0.000 description 3
238000007334 copolymerization reaction Methods 0.000 description 3
239000010949 copper Substances 0.000 description 3
239000007822 coupling agent Substances 0.000 description 3
MGNZXYYWBUKAII-UHFFFAOYSA-N cyclohexa-1,3-diene Chemical class C1CC=CC=C1 MGNZXYYWBUKAII-UHFFFAOYSA-N 0.000 description 3
238000007872 degassing Methods 0.000 description 3
150000005690 diesters Chemical class 0.000 description 3
125000003700 epoxy group Chemical group 0.000 description 3
239000011521 glass Substances 0.000 description 3
PYGSKMBEVAICCR-UHFFFAOYSA-N hexa-1,5-diene Chemical compound C=CCCC=C PYGSKMBEVAICCR-UHFFFAOYSA-N 0.000 description 3
150000002431 hydrogen Chemical class 0.000 description 3
239000011261 inert gas Substances 0.000 description 3
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 3
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238000012360 testing method Methods 0.000 description 3
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JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 3
239000010456 wollastonite Substances 0.000 description 3
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RRKODOZNUZCUBN-CCAGOZQPSA-N (1z,3z)-cycloocta-1,3-diene Chemical class C1CC\C=C/C=C\C1 RRKODOZNUZCUBN-CCAGOZQPSA-N 0.000 description 2
MRERMGPPCLQIPD-NBVRZTHBSA-N (3beta,5alpha,9alpha,22E,24R)-3,5,9-Trihydroxy-23-methylergosta-7,22-dien-6-one Chemical compound C1C(O)CCC2(C)C(CCC3(C(C(C)/C=C(\C)C(C)C(C)C)CCC33)C)(O)C3=CC(=O)C21O MRERMGPPCLQIPD-NBVRZTHBSA-N 0.000 description 2
PRBHEGAFLDMLAL-GQCTYLIASA-N (4e)-hexa-1,4-diene Chemical compound C\C=C\CC=C PRBHEGAFLDMLAL-GQCTYLIASA-N 0.000 description 2
PMJHHCWVYXUKFD-SNAWJCMRSA-N (E)-1,3-pentadiene Chemical compound C\C=C\C=C PMJHHCWVYXUKFD-SNAWJCMRSA-N 0.000 description 2
DSAYAFZWRDYBQY-UHFFFAOYSA-N 2,5-dimethylhexa-1,5-diene Chemical compound CC(=C)CCC(C)=C DSAYAFZWRDYBQY-UHFFFAOYSA-N 0.000 description 2
HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 2
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150000002762 monocarboxylic acid derivatives Chemical class 0.000 description 1
150000002763 monocarboxylic acids Chemical class 0.000 description 1
YIMHRDBSVCPJOV-UHFFFAOYSA-N n'-(2-ethoxyphenyl)-n-(2-ethylphenyl)oxamide Chemical compound CCOC1=CC=CC=C1NC(=O)C(=O)NC1=CC=CC=C1CC YIMHRDBSVCPJOV-UHFFFAOYSA-N 0.000 description 1
FTWUXYZHDFCGSV-UHFFFAOYSA-N n,n'-diphenyloxamide Chemical compound C=1C=CC=CC=1NC(=O)C(=O)NC1=CC=CC=C1 FTWUXYZHDFCGSV-UHFFFAOYSA-N 0.000 description 1
GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
239000012454 non-polar solvent Substances 0.000 description 1
JFNLZVQOOSMTJK-KNVOCYPGSA-N norbornene Chemical compound C1[C@@H]2CC[C@H]1C=C2 JFNLZVQOOSMTJK-KNVOCYPGSA-N 0.000 description 1
229920001778 nylon Polymers 0.000 description 1
QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
SOWBFZRMHSNYGE-UHFFFAOYSA-N oxamic acid Chemical class NC(=O)C(O)=O SOWBFZRMHSNYGE-UHFFFAOYSA-N 0.000 description 1
230000001590 oxidative effect Effects 0.000 description 1
MPQXHAGKBWFSNV-UHFFFAOYSA-N oxidophosphanium Chemical class [PH3]=O MPQXHAGKBWFSNV-UHFFFAOYSA-N 0.000 description 1
DXGLGDHPHMLXJC-UHFFFAOYSA-N oxybenzone Chemical compound OC1=CC(OC)=CC=C1C(=O)C1=CC=CC=C1 DXGLGDHPHMLXJC-UHFFFAOYSA-N 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
XYJRXVWERLGGKC-UHFFFAOYSA-D pentacalcium;hydroxide;triphosphate Chemical compound [OH-].[Ca+2].[Ca+2].[Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O XYJRXVWERLGGKC-UHFFFAOYSA-D 0.000 description 1
WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
125000005327 perimidinyl group Chemical group N1C(=NC2=CC=CC3=CC=CC1=C23)* 0.000 description 1
150000002978 peroxides Chemical class 0.000 description 1
125000004934 phenanthridinyl group Chemical group C1(=CC=CC2=NC=C3C=CC=CC3=C12)* 0.000 description 1
125000004625 phenanthrolinyl group Chemical group N1=C(C=CC2=CC=C3C=CC=NC3=C12)* 0.000 description 1
125000005561 phenanthryl group Chemical group 0.000 description 1
125000001791 phenazinyl group Chemical group C1(=CC=CC2=NC3=CC=CC=C3N=C12)* 0.000 description 1
239000002530 phenolic antioxidant Substances 0.000 description 1
125000001484 phenothiazinyl group Chemical group C1(=CC=CC=2SC3=CC=CC=C3NC12)* 0.000 description 1
125000005954 phenoxathiinyl group Chemical group 0.000 description 1
125000001644 phenoxazinyl group Chemical group C1(=CC=CC=2OC3=CC=CC=C3NC12)* 0.000 description 1
ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
ACVYVLVWPXVTIT-UHFFFAOYSA-N phosphinic acid Chemical class O[PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-N 0.000 description 1
235000011007 phosphoric acid Nutrition 0.000 description 1
150000003016 phosphoric acids Chemical class 0.000 description 1
150000003053 piperidines Chemical class 0.000 description 1
PMJHHCWVYXUKFD-UHFFFAOYSA-N piperylene Natural products CC=CC=C PMJHHCWVYXUKFD-UHFFFAOYSA-N 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
239000004033 plastic Substances 0.000 description 1
239000004014 plasticizer Substances 0.000 description 1
229920001484 poly(alkylene) Polymers 0.000 description 1
229920002285 poly(styrene-co-acrylonitrile) Polymers 0.000 description 1
229920000058 polyacrylate Polymers 0.000 description 1
229920013639 polyalphaolefin Polymers 0.000 description 1
238000006068 polycondensation reaction Methods 0.000 description 1
229920000728 polyester Polymers 0.000 description 1
229920000570 polyether Polymers 0.000 description 1
229920001195 polyisoprene Polymers 0.000 description 1
230000000379 polymerizing effect Effects 0.000 description 1
229920002223 polystyrene Polymers 0.000 description 1
229920001343 polytetrafluoroethylene Polymers 0.000 description 1
229920002635 polyurethane Polymers 0.000 description 1
239000004814 polyurethane Substances 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
HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
KOPQZJAYZFAPBC-UHFFFAOYSA-N propanoyl propaneperoxoate Chemical compound CCC(=O)OOC(=O)CC KOPQZJAYZFAPBC-UHFFFAOYSA-N 0.000 description 1
229940095574 propionic acid Drugs 0.000 description 1
239000003223 protective agent Substances 0.000 description 1
238000000746 purification Methods 0.000 description 1
125000000561 purinyl group Chemical group N1=C(N=C2N=CNC2=C1)* 0.000 description 1
125000003373 pyrazinyl group Chemical group 0.000 description 1
125000003226 pyrazolyl group Chemical group 0.000 description 1
125000002098 pyridazinyl group Chemical group 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
125000000714 pyrimidinyl group Chemical group 0.000 description 1
150000003235 pyrrolidines Chemical class 0.000 description 1
125000000168 pyrrolyl group Chemical group 0.000 description 1
239000010453 quartz Substances 0.000 description 1
150000004053 quinones Chemical class 0.000 description 1
229920005604 random copolymer Polymers 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
230000002040 relaxant effect Effects 0.000 description 1
GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 1
YGSDEFSMJLZEOE-UHFFFAOYSA-M salicylate Chemical compound OC1=CC=CC=C1C([O-])=O YGSDEFSMJLZEOE-UHFFFAOYSA-M 0.000 description 1
229960001860 salicylate Drugs 0.000 description 1
229940116351 sebacate Drugs 0.000 description 1
CXMXRPHRNRROMY-UHFFFAOYSA-L sebacate(2-) Chemical compound [O-]C(=O)CCCCCCCCC([O-])=O CXMXRPHRNRROMY-UHFFFAOYSA-L 0.000 description 1
150000003336 secondary aromatic amines Chemical class 0.000 description 1
229920006012 semi-aromatic polyamide Polymers 0.000 description 1
229920006114 semi-crystalline semi-aromatic polyamide Polymers 0.000 description 1
230000035945 sensitivity Effects 0.000 description 1
229920002379 silicone rubber Polymers 0.000 description 1
239000011734 sodium Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000003549 soybean oil Substances 0.000 description 1
235000012424 soybean oil Nutrition 0.000 description 1
239000011029 spinel Substances 0.000 description 1
229910052596 spinel Inorganic materials 0.000 description 1
230000000087 stabilizing effect Effects 0.000 description 1
229920006301 statistical copolymer Polymers 0.000 description 1
125000004079 stearyl 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])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
150000003440 styrenes Chemical class 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
229910052717 sulfur Inorganic materials 0.000 description 1
239000011593 sulfur Substances 0.000 description 1
239000000725 suspension Substances 0.000 description 1
238000010557 suspension polymerization reaction Methods 0.000 description 1
229920003051 synthetic elastomer Polymers 0.000 description 1
229920001059 synthetic polymer Polymers 0.000 description 1
239000005061 synthetic rubber Substances 0.000 description 1
229940042055 systemic antimycotics triazole derivative Drugs 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
KXYJPVZMZBJJBZ-UHFFFAOYSA-N tert-butyl 2-ethylbutaneperoxoate Chemical compound CCC(CC)C(=O)OOC(C)(C)C KXYJPVZMZBJJBZ-UHFFFAOYSA-N 0.000 description 1
SJMYWORNLPSJQO-UHFFFAOYSA-N tert-butyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC(C)(C)C SJMYWORNLPSJQO-UHFFFAOYSA-N 0.000 description 1
PFBLRDXPNUJYJM-UHFFFAOYSA-N tert-butyl 2-methylpropaneperoxoate Chemical compound CC(C)C(=O)OOC(C)(C)C PFBLRDXPNUJYJM-UHFFFAOYSA-N 0.000 description 1
GJBRNHKUVLOCEB-UHFFFAOYSA-N tert-butyl benzenecarboperoxoate Chemical compound CC(C)(C)OOC(=O)C1=CC=CC=C1 GJBRNHKUVLOCEB-UHFFFAOYSA-N 0.000 description 1
SWAXTRYEYUTSAP-UHFFFAOYSA-N tert-butyl ethaneperoxoate Chemical compound CC(=O)OOC(C)(C)C SWAXTRYEYUTSAP-UHFFFAOYSA-N 0.000 description 1
150000003512 tertiary amines Chemical class 0.000 description 1
UFDHBDMSHIXOKF-UHFFFAOYSA-N tetrahydrophthalic acid Natural products OC(=O)C1=C(C(O)=O)CCCC1 UFDHBDMSHIXOKF-UHFFFAOYSA-N 0.000 description 1
NQRYJNQNLNOLGT-UHFFFAOYSA-N tetrahydropyridine hydrochloride Natural products C1CCNCC1 NQRYJNQNLNOLGT-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
238000005979 thermal decomposition reaction Methods 0.000 description 1
229920006345 thermoplastic polyamide Polymers 0.000 description 1
229920006346 thermoplastic polyester elastomer Polymers 0.000 description 1
125000004627 thianthrenyl group Chemical group C1(=CC=CC=2SC3=CC=CC=C3SC12)* 0.000 description 1
238000004448 titration Methods 0.000 description 1
235000010384 tocopherol Nutrition 0.000 description 1
229960001295 tocopherol Drugs 0.000 description 1
229930003799 tocopherol Natural products 0.000 description 1
239000011732 tocopherol Substances 0.000 description 1
125000003944 tolyl group Chemical group 0.000 description 1
230000007704 transition Effects 0.000 description 1
238000004627 transmission electron microscopy Methods 0.000 description 1
150000003918 triazines Chemical class 0.000 description 1
IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
CMPGARWFYBADJI-UHFFFAOYSA-L tungstic acid Chemical compound O[W](O)(=O)=O CMPGARWFYBADJI-UHFFFAOYSA-L 0.000 description 1
238000000870 ultraviolet spectroscopy Methods 0.000 description 1
125000001834 xanthenyl group Chemical group C1=CC=CC=2OC3=CC=CC=C3C(C12)* 0.000 description 1
239000004246 zinc acetate Substances 0.000 description 1
239000011787 zinc oxide Substances 0.000 description 1
XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 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
GVJHHUAWPYXKBD-IEOSBIPESA-N α-tocopherol Chemical compound OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-IEOSBIPESA-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
- C08G67/00—Macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing oxygen or oxygen and carbon, not provided for in groups C08G2/00 - C08G65/00
- C08G67/02—Copolymers of carbon monoxide and aliphatic unsaturated compounds
- 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
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L59/00—Compositions of polyacetals; Compositions of derivatives of polyacetals

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)

DE1999106018 1999-02-16 1999-02-16 Polymerblends aus funktionalisierten Kohlenmonoxidcopolymeren und Polyamiden Withdrawn DE19906018A1 (de)

Priority Applications (3)

Application Number	Priority Date	Filing Date	Title
DE1999106018 DE19906018A1 (de)	1999-02-16	1999-02-16	Polymerblends aus funktionalisierten Kohlenmonoxidcopolymeren und Polyamiden
PCT/EP2000/000912 WO2000049088A1 (fr)	1999-02-16	2000-02-05	Melanges polymeres a base de copolymeres de monoxyde de carbone fonctionnalises et de polyamides
AU29067/00A AU2906700A (en)	1999-02-16	2000-02-05	Polymer blends made of functionalised carbon monoxide copolymers and polyamides

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE1999106018 DE19906018A1 (de)	1999-02-16	1999-02-16	Polymerblends aus funktionalisierten Kohlenmonoxidcopolymeren und Polyamiden

Publications (1)

Publication Number	Publication Date
DE19906018A1 true DE19906018A1 (de)	2000-08-17

Family

ID=7897386

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DE1999106018 Withdrawn DE19906018A1 (de)	1999-02-16	1999-02-16	Polymerblends aus funktionalisierten Kohlenmonoxidcopolymeren und Polyamiden

Country Status (3)

Country	Link
AU (1)	AU2906700A (fr)
DE (1)	DE19906018A1 (fr)
WO (1)	WO2000049088A1 (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE10162968B4 (de) *	2000-12-29	2008-07-10	Hyundai Motor Co.	Polyamidharz-Zusammensetzung und daraus hergestelltes synthetisches Harzprodukt

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US8071220B2 (en)	2006-07-21	2011-12-06	Exxonmobil Chemical Patents Inc.	Thermoplastic vulcanizates having improved adhesion to polar substrates

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS5838751A (ja) *	1981-08-21	1983-03-07	イ−・アイ・デユポン・デ・ニモアス・アンド・カンパニ−	強靭化されたポリアミドブレンド物
EP0339745B1 (fr) *	1988-04-29	1995-01-18	Shell Internationale Researchmaatschappij B.V.	Compositions de polycétones
US5466780A (en) *	1994-03-30	1995-11-14	Exxon Chemical Patents Inc.	Process for converting polyketones to polyesters
DE19811123A1 (de) *	1998-03-16	1999-09-23	Basf Ag	Derivatisierte Kohlenmonoxideopolymerisate

1999
- 1999-02-16 DE DE1999106018 patent/DE19906018A1/de not_active Withdrawn
2000
- 2000-02-05 WO PCT/EP2000/000912 patent/WO2000049088A1/fr not_active Ceased
- 2000-02-05 AU AU29067/00A patent/AU2906700A/en not_active Abandoned

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE10162968B4 (de) *	2000-12-29	2008-07-10	Hyundai Motor Co.	Polyamidharz-Zusammensetzung und daraus hergestelltes synthetisches Harzprodukt

Also Published As

Publication number	Publication date
WO2000049088A1 (fr)	2000-08-24
AU2906700A (en)	2000-09-04

Publication	Publication Date	Title
EP0654505B1 (fr)	1999-03-03	Compositions de polyphénylenéther et polyamide pour la fabrication d'articles par soufflage, extrusion de profile ou extrusion tubulaire
EP2121833B1 (fr)	2010-10-06	Masses moulables dont la résilience a une anisotropie réduite
EP0416436B1 (fr)	1993-11-03	Masses à mouler thermoplastique contenant des charges
EP2393877B1 (fr)	2012-12-05	Matières à mouler thermoplastiques contenant des copolymères de styrène et des polyamides
EP1242538B1 (fr)	2004-09-08	Matieres moulables thermoplastiques a comportement au traitement ameliore a base de polyarylene-ether-sulfones et de polyamides
EP0678555B1 (fr)	1998-07-01	Masses à mouler à base des poly(oxyphénylènes) et des polyamides
EP0607812B1 (fr)	1998-04-01	Masses à mouler en polyamide colorées en noir et iguifugées
DE10020785A1 (de)	2001-10-31	Polyarylethersulfon/Polyamid-Blends mit verbesserter Zähigkeit und Fließfähigkeit
EP0737719B1 (fr)	2002-08-21	Compositions thermoplastiques à base de polyamides aromatiques partiels et polyétherimides
EP0702058B1 (fr)	1999-10-06	Mélange à mouler composé d'éthers polyaryleniques et de copolyamides
EP0722986B1 (fr)	2000-04-19	Compositions de polyamides thermoplastiques
EP0694583B1 (fr)	2000-01-05	Alliages de polyamide/polyoléfine
DE4444378A1 (de)	1996-06-20	Thermoplastische Formmassen auf der Basis von teilaromatischen Polyamiden und Polymethacrylimiden
DE19906018A1 (de)	2000-08-17	Polymerblends aus funktionalisierten Kohlenmonoxidcopolymeren und Polyamiden
EP1105437B1 (fr)	2004-11-03	Matieres moulables a base de polyarylenethersulfones et de polyamides aliphatiques
EP0590392B1 (fr)	1997-06-04	Masses à mouler à base de polyaryléthers et de copolyamides partiellement aromatiques modifiés résistants aux chocs
DE4114455A1 (de)	1992-11-05	Thermoplastische formmasse auf der basis von polyarylethern, polyamiden und modifizierten polyarylethern als haftvermittler
DE19607187A1 (de)	1996-08-29	Thermoplastische Harzmasse
WO2003033594A1 (fr)	2003-04-24	Matieres a mouler thermoplastiques a base de sulfones de polyarylene ether
EP0480228A2 (fr)	1992-04-15	Masses à mouler thermoplastiques à base de polyamide
DE4127720A1 (de)	1993-02-25	Fliessfaehige thermoplastische formmassen
WO2001064792A1 (fr)	2001-09-07	Matieres moulables a base de polyarylenethersulfones et de polyamides possedant des groupes terminaux de piperidine
EP1056797B1 (fr)	2002-05-08	Procede de preparation de melanges polymeres a base d'aminonitriles et de polymeres thermoplastiques
DE19736973A1 (de)	1999-03-04	Formmassen auf der Basis von Polyarylenethern und Polyamiden
DE19737959A1 (de)	1999-03-04	Thermoplastische Formmassen auf Basis von Polyamid und Styrol/Diphenylethylen-Copolymeren

Legal Events

Date	Code	Title	Description
2001-05-31	8130	Withdrawal

DE19906018A1 - Polymerblends aus funktionalisierten Kohlenmonoxidcopolymeren und Polyamiden - Google Patents

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Priority Applications (3)

Applications Claiming Priority (1)

Publications (1)

Family

ID=7897386

Family Applications (1)

Country Status (3)

Cited By (1)

Families Citing this family (1)

Family Cites Families (4)

Cited By (1)

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