PH26191A - Moulding composition comprising a thermoset component and thermoplast component - Google Patents

Moulding composition comprising a thermoset component and thermoplast component Download PDF

Info

Publication number: PH26191A
Authority: PH; Philippines
Prior art keywords: component; precursor; composition; thermoset; polyarylsulphone
Prior art date: 1988-10-05

Application number

PH39317A

Other languages

English (en)

Inventor

Martin Thomas Choate

Patrick Terence Mcgrail

Mark Stephen Safton

Jeffrey Thomas Carter

Original Assignee

Ici Plc

Ici Compositions Inc

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.)

1988-10-05

Filing date

1989-10-02

Publication date

1992-03-18

1989-10-02 Application filed by Ici Plc, Ici Compositions Inc filed Critical Ici Plc

1992-03-18 Publication of PH26191A publication Critical patent/PH26191A/en

Links

239000000203 mixture Substances 0.000 title claims abstract description 80
229920001187 thermosetting polymer Polymers 0.000 title claims abstract description 33
238000000465 moulding Methods 0.000 title claims abstract description 21
239000002243 precursor Substances 0.000 claims abstract description 44
239000004634 thermosetting polymer Substances 0.000 claims abstract description 14
230000009969 flowable effect Effects 0.000 claims abstract description 11
239000007787 solid Substances 0.000 claims abstract description 11
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims abstract description 10
239000000853 adhesive Substances 0.000 claims abstract description 9
239000000126 substance Substances 0.000 claims abstract description 7
125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims abstract description 5
150000003568 thioethers Chemical class 0.000 claims abstract description 5
125000002947 alkylene group Chemical group 0.000 claims abstract description 4
125000002029 aromatic hydrocarbon group Chemical group 0.000 claims abstract 2
229920005989 resin Polymers 0.000 claims description 23
239000011347 resin Substances 0.000 claims description 23
239000003822 epoxy resin Substances 0.000 claims description 13
229920000647 polyepoxide Polymers 0.000 claims description 13
239000003795 chemical substances by application Substances 0.000 claims description 10
239000000945 filler Substances 0.000 claims description 9
238000006243 chemical reaction Methods 0.000 claims description 8
238000002156 mixing Methods 0.000 claims description 7
KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 claims description 6
238000004519 manufacturing process Methods 0.000 claims description 6
229920001568 phenolic resin Polymers 0.000 claims description 6
238000001746 injection moulding Methods 0.000 claims description 5
238000000034 method Methods 0.000 claims description 5
239000005011 phenolic resin Substances 0.000 claims description 5
238000000748 compression moulding Methods 0.000 claims description 4
ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 4
230000001070 adhesive effect Effects 0.000 claims description 3
238000013329 compounding Methods 0.000 claims description 2
238000005098 hot rolling Methods 0.000 claims description 2
238000001721 transfer moulding Methods 0.000 claims description 2
229920001169 thermoplastic Polymers 0.000 claims 10
239000004416 thermosoftening plastic Substances 0.000 claims 10
150000004945 aromatic hydrocarbons Chemical class 0.000 claims 1
239000010419 fine particle Substances 0.000 claims 1
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 12
229920000642 polymer Polymers 0.000 description 12
239000004593 Epoxy Substances 0.000 description 11
239000000243 solution Substances 0.000 description 11
239000000843 powder Substances 0.000 description 10
239000000835 fiber Substances 0.000 description 9
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 7
239000003054 catalyst Substances 0.000 description 7
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
230000015572 biosynthetic process Effects 0.000 description 6
239000007788 liquid Substances 0.000 description 6
229920003986 novolac Polymers 0.000 description 6
238000003786 synthesis reaction Methods 0.000 description 6
150000001412 amines Chemical class 0.000 description 5
229910052799 carbon Inorganic materials 0.000 description 5
239000003365 glass fiber Substances 0.000 description 5
239000000463 material Substances 0.000 description 5
230000000269 nucleophilic effect Effects 0.000 description 5
239000002904 solvent Substances 0.000 description 5
KUBDPQJOLOUJRM-UHFFFAOYSA-N 2-(chloromethyl)oxirane;4-[2-(4-hydroxyphenyl)propan-2-yl]phenol Chemical compound ClCC1CO1.C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 KUBDPQJOLOUJRM-UHFFFAOYSA-N 0.000 description 4
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
-1 phenols cyanate Chemical class 0.000 description 4
238000002360 preparation method Methods 0.000 description 4
238000007493 shaping process Methods 0.000 description 4
229930185605 Bisphenol Natural products 0.000 description 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 3
229920001971 elastomer Polymers 0.000 description 3
238000001125 extrusion Methods 0.000 description 3
239000010439 graphite Substances 0.000 description 3
229910002804 graphite Inorganic materials 0.000 description 3
VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical compound C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 description 3
RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 3
238000009863 impact test Methods 0.000 description 3
239000000314 lubricant Substances 0.000 description 3
239000000049 pigment Substances 0.000 description 3
229920002492 poly(sulfone) Polymers 0.000 description 3
239000005060 rubber Substances 0.000 description 3
GQWWGRUJOCIUKI-UHFFFAOYSA-N 2-[3-(2-methyl-1-oxopyrrolo[1,2-a]pyrazin-3-yl)propyl]guanidine Chemical group O=C1N(C)C(CCCN=C(N)N)=CN2C=CC=C21 GQWWGRUJOCIUKI-UHFFFAOYSA-N 0.000 description 2
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 2
VPWNQTHUCYMVMZ-UHFFFAOYSA-N 4,4'-sulfonyldiphenol Chemical class C1=CC(O)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 VPWNQTHUCYMVMZ-UHFFFAOYSA-N 0.000 description 2
NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 2
ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 2
239000000654 additive Substances 0.000 description 2
239000011324 bead Substances 0.000 description 2
PXKLMJQFEQBVLD-UHFFFAOYSA-N bisphenol F Chemical compound C1=CC(O)=CC=C1CC1=CC=C(O)C=C1 PXKLMJQFEQBVLD-UHFFFAOYSA-N 0.000 description 2
WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 2
230000008859 change Effects 0.000 description 2
239000003086 colorant Substances 0.000 description 2
238000001816 cooling Methods 0.000 description 2
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ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
LIWAQLJGPBVORC-UHFFFAOYSA-N ethylmethylamine Chemical compound CCNC LIWAQLJGPBVORC-UHFFFAOYSA-N 0.000 description 2
239000005350 fused silica glass Substances 0.000 description 2
239000011521 glass Substances 0.000 description 2
229910052736 halogen Inorganic materials 0.000 description 2
150000002367 halogens Chemical class 0.000 description 2
150000002430 hydrocarbons Chemical group 0.000 description 2
239000004615 ingredient Substances 0.000 description 2
230000000977 initiatory effect Effects 0.000 description 2
239000012948 isocyanate Substances 0.000 description 2
150000002513 isocyanates Chemical class 0.000 description 2
229910052760 oxygen Inorganic materials 0.000 description 2
239000002245 particle Substances 0.000 description 2
150000002989 phenols Chemical class 0.000 description 2
IGALFTFNPPBUDN-UHFFFAOYSA-N phenyl-[2,3,4,5-tetrakis(oxiran-2-ylmethyl)phenyl]methanediamine Chemical compound C=1C(CC2OC2)=C(CC2OC2)C(CC2OC2)=C(CC2OC2)C=1C(N)(N)C1=CC=CC=C1 IGALFTFNPPBUDN-UHFFFAOYSA-N 0.000 description 2
239000004848 polyfunctional curative Substances 0.000 description 2
239000012744 reinforcing agent Substances 0.000 description 2
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
229920002554 vinyl polymer Polymers 0.000 description 2
OZUNPRDEUXITBO-UHFFFAOYSA-N 1-(4-chlorophenyl)sulfonyl-4-[4-(4-chlorophenyl)sulfonylphenyl]benzene Chemical group C1=CC(Cl)=CC=C1S(=O)(=O)C1=CC=C(C=2C=CC(=CC=2)S(=O)(=O)C=2C=CC(Cl)=CC=2)C=C1 OZUNPRDEUXITBO-UHFFFAOYSA-N 0.000 description 1
LXBGSDVWAMZHDD-UHFFFAOYSA-N 2-methyl-1h-imidazole Chemical compound CC1=NC=CN1 LXBGSDVWAMZHDD-UHFFFAOYSA-N 0.000 description 1
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
LJGHYPLBDBRCRZ-UHFFFAOYSA-N 3-(3-aminophenyl)sulfonylaniline Chemical compound NC1=CC=CC(S(=O)(=O)C=2C=C(N)C=CC=2)=C1 LJGHYPLBDBRCRZ-UHFFFAOYSA-N 0.000 description 1
NZGQHKSLKRFZFL-UHFFFAOYSA-N 4-(4-hydroxyphenoxy)phenol Chemical compound C1=CC(O)=CC=C1OC1=CC=C(O)C=C1 NZGQHKSLKRFZFL-UHFFFAOYSA-N 0.000 description 1
PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical class NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 description 1
TYOXIFXYEIILLY-UHFFFAOYSA-N 5-methyl-2-phenyl-1h-imidazole Chemical compound N1C(C)=CN=C1C1=CC=CC=C1 TYOXIFXYEIILLY-UHFFFAOYSA-N 0.000 description 1
206010067484 Adverse reaction Diseases 0.000 description 1
229910015900 BF3 Inorganic materials 0.000 description 1
229910052582 BN Inorganic materials 0.000 description 1
229920001342 Bakelite® Polymers 0.000 description 1
PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 description 1
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
239000004215 Carbon black (E152) Substances 0.000 description 1
239000004970 Chain extender Substances 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-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
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
239000005977 Ethylene Substances 0.000 description 1
KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
241000264877 Hippospongia communis Species 0.000 description 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
239000002841 Lewis acid Substances 0.000 description 1
PEEHTFAAVSWFBL-UHFFFAOYSA-N Maleimide Chemical compound O=C1NC(=O)C=C1 PEEHTFAAVSWFBL-UHFFFAOYSA-N 0.000 description 1
229920000877 Melamine resin Polymers 0.000 description 1
229910019142 PO4 Inorganic materials 0.000 description 1
239000004952 Polyamide Substances 0.000 description 1
239000004642 Polyimide Substances 0.000 description 1
229920000265 Polyparaphenylene Polymers 0.000 description 1
239000006087 Silane Coupling Agent Substances 0.000 description 1
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
239000005864 Sulphur Substances 0.000 description 1
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
238000010521 absorption reaction Methods 0.000 description 1
239000002253 acid Substances 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
229920006397 acrylic thermoplastic Polymers 0.000 description 1
230000004913 activation Effects 0.000 description 1
230000006838 adverse reaction Effects 0.000 description 1
239000003513 alkali Substances 0.000 description 1
229910000288 alkali metal carbonate Inorganic materials 0.000 description 1
150000008041 alkali metal carbonates Chemical class 0.000 description 1
HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 1
PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
125000003277 amino group Chemical group 0.000 description 1
150000004982 aromatic amines Chemical class 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
239000010425 asbestos Substances 0.000 description 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
239000004637 bakelite Substances 0.000 description 1
239000002585 base Substances 0.000 description 1
230000008901 benefit Effects 0.000 description 1
KTYQPSIVRZZBRC-UHFFFAOYSA-N benzene-1,3-diol benzene-1,4-diol 4-(4-hydroxyphenyl)phenol naphthalene-1,2-diol Chemical compound OC1=C(C2=CC=CC=C2C=C1)O.C1(O)=CC(O)=CC=C1.OC1=CC=C(C=C1)C1=CC=C(C=C1)O.C1(O)=CC=C(O)C=C1 KTYQPSIVRZZBRC-UHFFFAOYSA-N 0.000 description 1
239000004305 biphenyl Substances 0.000 description 1
235000010290 biphenyl Nutrition 0.000 description 1
125000002529 biphenylenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3C12)* 0.000 description 1
JRPRCOLKIYRSNH-UHFFFAOYSA-N bis(oxiran-2-ylmethyl) benzene-1,2-dicarboxylate Chemical compound C=1C=CC=C(C(=O)OCC2OC2)C=1C(=O)OCC1CO1 JRPRCOLKIYRSNH-UHFFFAOYSA-N 0.000 description 1
239000004841 bisphenol A epoxy resin Substances 0.000 description 1
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
229910052794 bromium Inorganic materials 0.000 description 1
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229910052918 calcium silicate Inorganic materials 0.000 description 1
239000003990 capacitor Substances 0.000 description 1
239000004202 carbamide Substances 0.000 description 1
125000004432 carbon atom Chemical group C* 0.000 description 1
150000001244 carboxylic acid anhydrides Chemical class 0.000 description 1
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239000000460 chlorine Substances 0.000 description 1
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150000001875 compounds Chemical class 0.000 description 1
239000004020 conductor Substances 0.000 description 1
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238000004132 cross linking Methods 0.000 description 1
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238000007865 diluting Methods 0.000 description 1
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235000010299 hexamethylene tetramine Nutrition 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
239000001257 hydrogen Substances 0.000 description 1
229910052739 hydrogen Inorganic materials 0.000 description 1
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OHQOKJPHNPUMLN-UHFFFAOYSA-N n,n'-diphenylmethanediamine Chemical compound C=1C=CC=CC=1NCNC1=CC=CC=C1 OHQOKJPHNPUMLN-UHFFFAOYSA-N 0.000 description 1
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229910052882 wollastonite Inorganic materials 0.000 description 1

Classifications

- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F02—COMBUSTION ENGINES; HOT-GAS OR COMBUSTION-PRODUCT ENGINE PLANTS
- F02F—CYLINDERS, PISTONS OR CASINGS, FOR COMBUSTION ENGINES; ARRANGEMENTS OF SEALINGS IN COMBUSTION ENGINES
- F02F7/00—Casings, e.g. crankcases
- F02F7/006—Camshaft or pushrod housings
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L61/00—Compositions of condensation polymers of aldehydes or ketones; Compositions of derivatives of such polymers
- C08L61/04—Condensation polymers of aldehydes or ketones with phenols only
- C08L61/06—Condensation polymers of aldehydes or ketones with phenols only of aldehydes with phenols
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L63/00—Compositions of epoxy resins; Compositions of derivatives of epoxy resins
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L81/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing sulfur with or without nitrogen, oxygen or carbon only; Compositions of polysulfones; Compositions of derivatives of such polymers
- C08L81/06—Polysulfones; Polyethersulfones
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F05—INDEXING SCHEMES RELATING TO ENGINES OR PUMPS IN VARIOUS SUBCLASSES OF CLASSES F01-F04
- F05C—INDEXING SCHEME RELATING TO MATERIALS, MATERIAL PROPERTIES OR MATERIAL CHARACTERISTICS FOR MACHINES, ENGINES OR PUMPS OTHER THAN NON-POSITIVE-DISPLACEMENT MACHINES OR ENGINES
- F05C2225/00—Synthetic polymers, e.g. plastics; Rubber
- F05C2225/08—Thermoplastics

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)
Mechanical Engineering (AREA)
Combustion & Propulsion (AREA)
General Engineering & Computer Science (AREA)
Compositions Of Macromolecular Compounds (AREA)
Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
Other Resins Obtained By Reactions Not Involving Carbon-To-Carbon Unsaturated Bonds (AREA)
Phenolic Resins Or Amino Resins (AREA)
Epoxy Resins (AREA)
Non-Metallic Protective Coatings For Printed Circuits (AREA)
Adhesives Or Adhesive Processes (AREA)
Macromonomer-Based Addition Polymer (AREA)

PH39317A 1988-10-05 1989-10-02 Moulding composition comprising a thermoset component and thermoplast component PH26191A (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US07/253,595 US4972031A (en)	1988-10-05	1988-10-05	Plastic moulding composition comprising an uncured or partly cured thermoset resin precursor and a polyarylsulphone

Publications (1)

Publication Number	Publication Date
PH26191A true PH26191A (en)	1992-03-18

Family

ID=22960921

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
PH39317A PH26191A (en)	1988-10-05	1989-10-02	Moulding composition comprising a thermoset component and thermoplast component

Country Status (10)

Country	Link
US (1)	US4972031A (fr)
EP (1)	EP0365168B1 (fr)
JP (2)	JP3231753B2 (fr)
KR (1)	KR0173973B1 (fr)
AT (1)	ATE180267T1 (fr)
DE (1)	DE68928998T2 (fr)
ES (1)	ES2134756T3 (fr)
GB (1)	GB8921770D0 (fr)
MY (1)	MY105596A (fr)
PH (1)	PH26191A (fr)

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GB0717507D0 (en)	2007-09-07	2007-10-17	Cytec Tech Corp	Composite materials and their use
CN102666641B (zh)	2009-12-17	2015-08-26	塞特克技术公司	工程热塑性塑料中的多功能添加剂
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JP5601191B2 (ja) *	2010-12-21	2014-10-08	住友ベークライト株式会社	摩擦材用フェノール樹脂組成物、変性フェノール樹脂の製造方法及び摩擦材
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1988
- 1988-10-05 US US07/253,595 patent/US4972031A/en not_active Expired - Lifetime
1989
- 1989-09-27 GB GB898921770A patent/GB8921770D0/en active Pending
- 1989-10-02 DE DE68928998T patent/DE68928998T2/de not_active Expired - Lifetime
- 1989-10-02 AT AT89310038T patent/ATE180267T1/de not_active IP Right Cessation
- 1989-10-02 PH PH39317A patent/PH26191A/en unknown
- 1989-10-02 ES ES89310038T patent/ES2134756T3/es not_active Expired - Lifetime
- 1989-10-02 EP EP89310038A patent/EP0365168B1/fr not_active Expired - Lifetime
- 1989-10-03 MY MYPI89001351A patent/MY105596A/en unknown
- 1989-10-04 JP JP25797989A patent/JP3231753B2/ja not_active Expired - Fee Related
- 1989-10-05 KR KR1019890014285A patent/KR0173973B1/ko not_active Expired - Fee Related
1998
- 1998-05-18 JP JP10135721A patent/JP3092103B2/ja not_active Expired - Fee Related

Also Published As

Publication number	Publication date
DE68928998T2 (de)	1999-10-28
DE68928998D1 (de)	1999-06-24
JP3092103B2 (ja)	2000-09-25
ATE180267T1 (de)	1999-06-15
EP0365168A2 (fr)	1990-04-25
MY105596A (en)	1994-11-30
KR0173973B1 (ko)	1999-04-01
KR910008082A (ko)	1991-05-30
EP0365168B1 (fr)	1999-05-19
JPH1180365A (ja)	1999-03-26
EP0365168A3 (fr)	1991-12-04
JPH0314872A (ja)	1991-01-23
ES2134756T3 (es)	1999-10-16
JP3231753B2 (ja)	2001-11-26
GB8921770D0 (en)	1989-11-08
US4972031A (en)	1990-11-20

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WO1995007309A1 (fr)	1995-03-16	Compositions de resines comprenant des esters de cyanate phenolique et des composes polyepoxydes