CA1262586A - Melanges de polyetherimides avec d'autres melanges d'acrylonitrile-butadiene-styrene - Google Patents

Melanges de polyetherimides avec d'autres melanges d'acrylonitrile-butadiene-styrene

Info

Publication number: CA1262586A
Authority: CA; Canada
Prior art keywords: blends; polyetherimide; butadiene; acrylonitrile; styrene
Prior art date: 1985-02-08
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

Application number

CA000473926A

Other languages

English (en)

Inventor

Harold F. Giles, Jr.

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.)

General Electric Co

Original Assignee

General Electric Co

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.)

1985-02-08

Filing date

1985-02-08

Publication date

1989-10-31

1985-02-08 Application filed by General Electric Co filed Critical General Electric Co

1985-02-08 Priority to CA000473926A priority Critical patent/CA1262586A/fr

1989-10-31 Application granted granted Critical

1989-10-31 Publication of CA1262586A publication Critical patent/CA1262586A/fr

Status Expired legal-status Critical Current

Links

239000000203 mixture Substances 0.000 title claims abstract description 34
229920001601 polyetherimide Polymers 0.000 title claims abstract description 31
229920002492 poly(sulfone) Polymers 0.000 title claims abstract description 12
229920000122 acrylonitrile butadiene styrene Polymers 0.000 title claims abstract description 11
XECAHXYUAAWDEL-UHFFFAOYSA-N acrylonitrile butadiene styrene Chemical compound C=CC=C.C=CC#N.C=CC1=CC=CC=C1 XECAHXYUAAWDEL-UHFFFAOYSA-N 0.000 title claims abstract description 10
239000004676 acrylonitrile butadiene styrene Substances 0.000 title claims abstract description 10
239000004697 Polyetherimide Substances 0.000 claims abstract description 17
125000004432 carbon atom Chemical group C* 0.000 claims description 3
229920003023 plastic Polymers 0.000 claims description 3
239000004033 plastic Substances 0.000 claims description 3
229920000412 polyarylene Polymers 0.000 claims description 3
229920000642 polymer Polymers 0.000 claims description 3
229920001169 thermoplastic Polymers 0.000 claims description 3
239000004416 thermosoftening plastic Substances 0.000 claims description 3
125000002947 alkylene group Chemical group 0.000 claims description 2
GTDPSWPPOUPBNX-UHFFFAOYSA-N ac1mqpva Chemical compound CC12C(=O)OC(=O)C1(C)C1(C)C2(C)C(=O)OC1=O GTDPSWPPOUPBNX-UHFFFAOYSA-N 0.000 description 13
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 12
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 6
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
-1 ether anhydride Chemical class 0.000 description 6
150000004985 diamines Chemical class 0.000 description 5
KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 4
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 3
125000003118 aryl group Chemical group 0.000 description 3
150000001875 compounds Chemical class 0.000 description 3
125000006159 dianhydride group Chemical group 0.000 description 3
238000000034 method Methods 0.000 description 3
239000001294 propane Substances 0.000 description 3
239000011347 resin Substances 0.000 description 3
229920005989 resin Polymers 0.000 description 3
239000004721 Polyphenylene oxide Substances 0.000 description 2
ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 2
125000000732 arylene group Chemical group 0.000 description 2
238000006243 chemical reaction Methods 0.000 description 2
229920001577 copolymer Polymers 0.000 description 2
USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 2
KZTYYGOKRVBIMI-UHFFFAOYSA-N diphenyl sulfone Chemical compound C=1C=CC=CC=1S(=O)(=O)C1=CC=CC=C1 KZTYYGOKRVBIMI-UHFFFAOYSA-N 0.000 description 2
238000002347 injection Methods 0.000 description 2
239000007924 injection Substances 0.000 description 2
RLSSMJSEOOYNOY-UHFFFAOYSA-N m-cresol Chemical compound CC1=CC=CC(O)=C1 RLSSMJSEOOYNOY-UHFFFAOYSA-N 0.000 description 2
239000000463 material Substances 0.000 description 2
VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
229920002857 polybutadiene Polymers 0.000 description 2
229920000570 polyether Polymers 0.000 description 2
238000006116 polymerization reaction Methods 0.000 description 2
239000002904 solvent Substances 0.000 description 2
150000003457 sulfones Chemical class 0.000 description 2
WZCQRUWWHSTZEM-UHFFFAOYSA-N 1,3-phenylenediamine Chemical compound NC1=CC=CC(N)=C1 WZCQRUWWHSTZEM-UHFFFAOYSA-N 0.000 description 1
OCJBOOLMMGQPQU-UHFFFAOYSA-N 1,4-dichlorobenzene Chemical compound ClC1=CC=C(Cl)C=C1 OCJBOOLMMGQPQU-UHFFFAOYSA-N 0.000 description 1
CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 1
PZKPUGIOJKNRQZ-UHFFFAOYSA-N 1-methylcyclohexa-3,5-diene-1,3-diamine Chemical compound CC1(N)CC(N)=CC=C1 PZKPUGIOJKNRQZ-UHFFFAOYSA-N 0.000 description 1
RLYCRLGLCUXUPO-UHFFFAOYSA-N 2,6-diaminotoluene Chemical compound CC1=C(N)C=CC=C1N RLYCRLGLCUXUPO-UHFFFAOYSA-N 0.000 description 1
QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 1
JRBJSXQPQWSCCF-UHFFFAOYSA-N 3,3'-Dimethoxybenzidine Chemical compound C1=C(N)C(OC)=CC(C=2C=C(OC)C(N)=CC=2)=C1 JRBJSXQPQWSCCF-UHFFFAOYSA-N 0.000 description 1
WQYOBFRCLOZCRC-UHFFFAOYSA-N 3-[4-[4-(2,3-dicarboxyphenoxy)benzoyl]phenoxy]phthalic acid Chemical compound OC(=O)C1=CC=CC(OC=2C=CC(=CC=2)C(=O)C=2C=CC(OC=3C(=C(C(O)=O)C=CC=3)C(O)=O)=CC=2)=C1C(O)=O WQYOBFRCLOZCRC-UHFFFAOYSA-N 0.000 description 1
GPXCORHXFPYJEH-UHFFFAOYSA-N 3-[[3-aminopropyl(dimethyl)silyl]oxy-dimethylsilyl]propan-1-amine Chemical compound NCCC[Si](C)(C)O[Si](C)(C)CCCN GPXCORHXFPYJEH-UHFFFAOYSA-N 0.000 description 1
YEEIWUUBRYZFEH-UHFFFAOYSA-N 3-methoxyhexane-1,6-diamine Chemical compound NCCC(OC)CCCN YEEIWUUBRYZFEH-UHFFFAOYSA-N 0.000 description 1
SGEWZUYVXQESSB-UHFFFAOYSA-N 3-methylheptane-1,7-diamine Chemical compound NCCC(C)CCCCN SGEWZUYVXQESSB-UHFFFAOYSA-N 0.000 description 1
ICNFHJVPAJKPHW-UHFFFAOYSA-N 4,4'-Thiodianiline Chemical compound C1=CC(N)=CC=C1SC1=CC=C(N)C=C1 ICNFHJVPAJKPHW-UHFFFAOYSA-N 0.000 description 1
YBRVSVVVWCFQMG-UHFFFAOYSA-N 4,4'-diaminodiphenylmethane Chemical compound C1=CC(N)=CC=C1CC1=CC=C(N)C=C1 YBRVSVVVWCFQMG-UHFFFAOYSA-N 0.000 description 1
ZWIBGDOHXGXHEV-UHFFFAOYSA-N 4,4-dimethylheptane-1,7-diamine Chemical compound NCCCC(C)(C)CCCN ZWIBGDOHXGXHEV-UHFFFAOYSA-N 0.000 description 1
JQGUWEUKOQRRJU-UHFFFAOYSA-N 4-(4-aminobutyl-methyl-trimethylsilyloxysilyl)butan-1-amine Chemical compound NCCCC[Si](C)(O[Si](C)(C)C)CCCCN JQGUWEUKOQRRJU-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
GAUNIEOSKKZOPV-UHFFFAOYSA-N 4-[4-[4-(3,4-dicarboxyphenoxy)benzoyl]phenoxy]phthalic acid Chemical compound C1=C(C(O)=O)C(C(=O)O)=CC=C1OC1=CC=C(C(=O)C=2C=CC(OC=3C=C(C(C(O)=O)=CC=3)C(O)=O)=CC=2)C=C1 GAUNIEOSKKZOPV-UHFFFAOYSA-N 0.000 description 1
BBTGUNMUUYNPLH-UHFFFAOYSA-N 5-[4-[(1,3-dioxo-2-benzofuran-5-yl)oxy]phenoxy]-2-benzofuran-1,3-dione Chemical compound C1=C2C(=O)OC(=O)C2=CC(OC2=CC=C(C=C2)OC=2C=C3C(=O)OC(C3=CC=2)=O)=C1 BBTGUNMUUYNPLH-UHFFFAOYSA-N 0.000 description 1
MQJKPEGWNLWLTK-UHFFFAOYSA-N Dapsone Chemical compound C1=CC(N)=CC=C1S(=O)(=O)C1=CC=C(N)C=C1 MQJKPEGWNLWLTK-UHFFFAOYSA-N 0.000 description 1
229920000459 Nitrile rubber Polymers 0.000 description 1
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
239000005062 Polybutadiene Substances 0.000 description 1
229910052783 alkali metal Inorganic materials 0.000 description 1
150000001340 alkali metals Chemical class 0.000 description 1
125000003277 amino group Chemical group 0.000 description 1
150000008064 anhydrides Chemical class 0.000 description 1
125000004429 atom Chemical group 0.000 description 1
HFACYLZERDEVSX-UHFFFAOYSA-N benzidine Chemical compound C1=CC(N)=CC=C1C1=CC=C(N)C=C1 HFACYLZERDEVSX-UHFFFAOYSA-N 0.000 description 1
235000010290 biphenyl Nutrition 0.000 description 1
239000004305 biphenyl Substances 0.000 description 1
125000006267 biphenyl group Chemical group 0.000 description 1
NTXGQCSETZTARF-UHFFFAOYSA-N buta-1,3-diene;prop-2-enenitrile Chemical compound C=CC=C.C=CC#N NTXGQCSETZTARF-UHFFFAOYSA-N 0.000 description 1
MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
229930003836 cresol Natural products 0.000 description 1
VKIRRGRTJUUZHS-UHFFFAOYSA-N cyclohexane-1,4-diamine Chemical compound NC1CCC(N)CC1 VKIRRGRTJUUZHS-UHFFFAOYSA-N 0.000 description 1
YQLZOAVZWJBZSY-UHFFFAOYSA-N decane-1,10-diamine Chemical compound NCCCCCCCCCCN YQLZOAVZWJBZSY-UHFFFAOYSA-N 0.000 description 1
229940117389 dichlorobenzene Drugs 0.000 description 1
230000000694 effects Effects 0.000 description 1
229920001971 elastomer Polymers 0.000 description 1
125000001033 ether group Chemical group 0.000 description 1
238000001125 extrusion Methods 0.000 description 1
230000009477 glass transition Effects 0.000 description 1
229920000578 graft copolymer Polymers 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
PWSKHLMYTZNYKO-UHFFFAOYSA-N heptane-1,7-diamine Chemical compound NCCCCCCCN PWSKHLMYTZNYKO-UHFFFAOYSA-N 0.000 description 1
125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
230000003993 interaction Effects 0.000 description 1
229940018564 m-phenylenediamine Drugs 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
239000000178 monomer Substances 0.000 description 1
KMBPCQSCMCEPMU-UHFFFAOYSA-N n'-(3-aminopropyl)-n'-methylpropane-1,3-diamine Chemical compound NCCCN(C)CCCN KMBPCQSCMCEPMU-UHFFFAOYSA-N 0.000 description 1
YYEIRLHVLCIHCN-UHFFFAOYSA-N n'-methylheptane-1,7-diamine Chemical compound CNCCCCCCCN YYEIRLHVLCIHCN-UHFFFAOYSA-N 0.000 description 1
LFBJWQBNKOIOMJ-UHFFFAOYSA-N n,n'-dimethylheptane-1,7-diamine Chemical compound CNCCCCCCCNC LFBJWQBNKOIOMJ-UHFFFAOYSA-N 0.000 description 1
KQSABULTKYLFEV-UHFFFAOYSA-N naphthalene-1,5-diamine Chemical compound C1=CC=C2C(N)=CC=CC2=C1N KQSABULTKYLFEV-UHFFFAOYSA-N 0.000 description 1
SXJVFQLYZSNZBT-UHFFFAOYSA-N nonane-1,9-diamine Chemical compound NCCCCCCCCCN SXJVFQLYZSNZBT-UHFFFAOYSA-N 0.000 description 1
VQXBKCWOCJSIRT-UHFFFAOYSA-N octadecane-1,12-diamine Chemical compound CCCCCCC(N)CCCCCCCCCCCN VQXBKCWOCJSIRT-UHFFFAOYSA-N 0.000 description 1
239000008188 pellet Substances 0.000 description 1
ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
SCUZVMOVTVSBLE-UHFFFAOYSA-N prop-2-enenitrile;styrene Chemical compound C=CC#N.C=CC1=CC=CC=C1 SCUZVMOVTVSBLE-UHFFFAOYSA-N 0.000 description 1
WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical group CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 description 1
239000005060 rubber Substances 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
239000007787 solid Substances 0.000 description 1
229920000638 styrene acrylonitrile Polymers 0.000 description 1
239000000126 substance Substances 0.000 description 1

Landscapes

Compositions Of Macromolecular Compounds (AREA)

CA000473926A 1985-02-08 1985-02-08 Melanges de polyetherimides avec d'autres melanges d'acrylonitrile-butadiene-styrene Expired CA1262586A (fr)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
CA000473926A CA1262586A (fr)	1985-02-08	1985-02-08	Melanges de polyetherimides avec d'autres melanges d'acrylonitrile-butadiene-styrene

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CA000473926A CA1262586A (fr)	1985-02-08	1985-02-08	Melanges de polyetherimides avec d'autres melanges d'acrylonitrile-butadiene-styrene

Publications (1)

Publication Number	Publication Date
CA1262586A true CA1262586A (fr)	1989-10-31

Family

ID=4129794

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA000473926A Expired CA1262586A (fr)	1985-02-08	1985-02-08	Melanges de polyetherimides avec d'autres melanges d'acrylonitrile-butadiene-styrene

Country Status (1)

Country	Link
CA (1)	CA1262586A (fr)

1985
- 1985-02-08 CA CA000473926A patent/CA1262586A/fr not_active Expired

Legal Events

Date	Code	Title	Description
1996-04-30	MKLA	Lapsed

Publication	Publication Date	Title
CA1177191A (fr)	1984-10-30	Melanges de polyetherimides et de copolymeres sequences d'organopolysiloxanne-polycarbonate
US5385970A (en)	1995-01-31	Halogen-free flame retardant ternary blends
US4663378A (en)	1987-05-05	Silicone-modified polyethermides
US5344910A (en)	1994-09-06	Heat-resistant polycarbonate resins containing 2-alkyl-3,3-bis(p-hydroxyphenyl)phthalimide
US5028681A (en)	1991-07-02	Novel poly(imide-siloxane) block copolymers and process for their preparation
KR960013127B1 (ko)	1996-09-30	폴리카아보네이트와 폴리아미드의 폴리머 블렌드 및 이의 제조방법
US4468506A (en)	1984-08-28	Polyetherimide blends
US4395518A (en)	1983-07-26	Polyetherimide-acrylate copolymer blends
US5157085A (en)	1992-10-20	Polyimide resin composition
US4393168A (en)	1983-07-12	Blends of polyetherimides and rubber modified vinyl aromatic polymers
WO1983003417A1 (fr)	1983-10-13	Melanges de polyetherimide-polysulfone
US4293684A (en)	1981-10-06	Polyetherimide having long chain aliphatic end groups and method for making
US4588779A (en)	1986-05-13	Modified polyetherimide resins
US5187228A (en)	1993-02-16	Stabilizer for compatibilized polycarbonate and polyamide polymer blends
US4390665A (en)	1983-06-28	Polyetherimide-EPDM terpolymer blends
US4481325A (en)	1984-11-06	Polyalkylenelactone modified polyetherimides
CA1192692A (fr)	1985-08-27	Melanges polytetherimide-polypropylene
EP0691380B1 (fr)	1999-09-01	Résines de polyétherimide modifiées aux chocs
WO1993004109A1 (fr)	1993-03-04	Compositions de copolymeres de polyetherimidesiloxane renfermant un homopolymere de polyetherimide a fort ecoulement a l'etat fondu
EP0091116B1 (fr)	1986-10-15	Mélanges de polyétherimides
EP0131643B1 (fr)	1988-02-17	Mélange polyéthérimide-polycarbonate
US5019625A (en)	1991-05-28	Compatibilizing agent for polycarbonate and polyamide polymer blends
EP0156028A1 (fr)	1985-10-02	Mélanges de polyétherimides avec des mélanges acrylonitrile-butadiène-styrène/polysulfone
WO1984003893A1 (fr)	1984-10-11	Melanges de polyetherimide et de terpolymere epdm
AU1556183A (en)	1984-10-25	Polyetherimide-epdm terpolymer blend