NO753016L - - Google Patents

Info

Publication number: NO753016L
Authority: NO; Norway
Prior art keywords: weight; mixture; unsaturated; stated; mass
Prior art date: 1974-09-03

Application number

NO753016A

Other languages

English (en)

Norwegian (no)

Inventor

M G Roberts

C E Bolen

Original Assignee

Owens Corning Fiberglass Corp

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.)

1974-09-03

Filing date

1975-09-02

Publication date

1976-03-04

1975-09-02 Application filed by Owens Corning Fiberglass Corp filed Critical Owens Corning Fiberglass Corp

1976-03-04 Publication of NO753016L publication Critical patent/NO753016L/no

Links

239000000203 mixture Substances 0.000 claims description 80
229920001169 thermoplastic Polymers 0.000 claims description 55
239000004416 thermosoftening plastic Substances 0.000 claims description 53
229920000642 polymer Polymers 0.000 claims description 37
239000000178 monomer Substances 0.000 claims description 33
229920000728 polyester Polymers 0.000 claims description 33
229920001971 elastomer Polymers 0.000 claims description 23
239000000806 elastomer Substances 0.000 claims description 23
150000001875 compounds Chemical class 0.000 claims description 17
239000007788 liquid Substances 0.000 claims description 16
238000000465 moulding Methods 0.000 claims description 15
238000006116 polymerization reaction Methods 0.000 claims description 12
238000000034 method Methods 0.000 claims description 11
229920001187 thermosetting polymer Polymers 0.000 claims description 11
238000004519 manufacturing process Methods 0.000 claims description 10
239000007787 solid Substances 0.000 claims description 7
229920003048 styrene butadiene rubber Polymers 0.000 claims description 7
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 6
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 6
238000003825 pressing Methods 0.000 claims description 6
229920002857 polybutadiene Polymers 0.000 claims description 5
150000007524 organic acids Chemical class 0.000 claims description 4
239000005062 Polybutadiene Substances 0.000 claims description 3
239000007795 chemical reaction product Substances 0.000 claims description 3
239000003431 cross linking reagent Substances 0.000 claims description 3
150000001993 dienes Chemical class 0.000 claims description 3
239000003349 gelling agent Substances 0.000 claims description 3
239000003365 glass fiber Substances 0.000 claims description 3
KGIGUEBEKRSTEW-UHFFFAOYSA-N 2-vinylpyridine Chemical compound C=CC1=CC=CC=N1 KGIGUEBEKRSTEW-UHFFFAOYSA-N 0.000 claims description 2
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims description 2
JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 claims description 2
229920002121 Hydroxyl-terminated polybutadiene Polymers 0.000 claims description 2
PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 claims description 2
BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 claims 2
239000011521 glass Substances 0.000 claims 1
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 28
QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 8
238000006243 chemical reaction Methods 0.000 description 8
239000000047 product Substances 0.000 description 8
229920006305 unsaturated polyester Polymers 0.000 description 8
CNHDIAIOKMXOLK-UHFFFAOYSA-N toluquinol Chemical compound CC1=CC(O)=CC=C1O CNHDIAIOKMXOLK-UHFFFAOYSA-N 0.000 description 7
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
239000002253 acid Substances 0.000 description 6
239000004342 Benzoyl peroxide Substances 0.000 description 5
OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 5
235000019400 benzoyl peroxide Nutrition 0.000 description 5
239000000463 material Substances 0.000 description 5
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
238000002156 mixing Methods 0.000 description 4
239000011541 reaction mixture Substances 0.000 description 4
OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 3
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
238000002360 preparation method Methods 0.000 description 3
PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 2
SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 2
VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 2
150000001298 alcohols Chemical class 0.000 description 2
230000000052 comparative effect Effects 0.000 description 2
229920001577 copolymer Polymers 0.000 description 2
150000001991 dicarboxylic acids Chemical class 0.000 description 2
239000000945 filler Substances 0.000 description 2
229920000578 graft copolymer Polymers 0.000 description 2
239000003999 initiator Substances 0.000 description 2
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 2
229910052757 nitrogen Inorganic materials 0.000 description 2
229920001084 poly(chloroprene) Polymers 0.000 description 2
229920001195 polyisoprene Polymers 0.000 description 2
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
WDCYWAQPCXBPJA-UHFFFAOYSA-N 1,3-dinitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC([N+]([O-])=O)=C1 WDCYWAQPCXBPJA-UHFFFAOYSA-N 0.000 description 1
OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
239000002174 Styrene-butadiene Substances 0.000 description 1
BGNXCDMCOKJUMV-UHFFFAOYSA-N Tert-Butylhydroquinone Chemical compound CC(C)(C)C1=CC(O)=CC=C1O BGNXCDMCOKJUMV-UHFFFAOYSA-N 0.000 description 1
150000008065 acid anhydrides Chemical class 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
150000008064 anhydrides Chemical class 0.000 description 1
VPTUCBHUUKXFOX-UHFFFAOYSA-N benzene-1,4-diol;styrene Chemical compound C=CC1=CC=CC=C1.OC1=CC=C(O)C=C1 VPTUCBHUUKXFOX-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
229910000019 calcium carbonate Inorganic materials 0.000 description 1
150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
239000011248 coating agent Substances 0.000 description 1
238000000576 coating method Methods 0.000 description 1
239000002131 composite material Substances 0.000 description 1
239000013068 control sample Substances 0.000 description 1
SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
239000001530 fumaric acid Substances 0.000 description 1
238000001879 gelation Methods 0.000 description 1
VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 1
239000000347 magnesium hydroxide Substances 0.000 description 1
229910001862 magnesium hydroxide Inorganic materials 0.000 description 1
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
239000011976 maleic acid Substances 0.000 description 1
239000011159 matrix material Substances 0.000 description 1
238000012986 modification Methods 0.000 description 1
230000004048 modification Effects 0.000 description 1
230000019612 pigmentation Effects 0.000 description 1
239000011505 plaster Substances 0.000 description 1
239000004033 plastic Substances 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
239000004848 polyfunctional curative Substances 0.000 description 1
230000000379 polymerizing effect Effects 0.000 description 1
HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
239000011347 resin Substances 0.000 description 1
229920005989 resin Polymers 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
239000002904 solvent Substances 0.000 description 1
239000011115 styrene butadiene Substances 0.000 description 1
239000000126 substance Substances 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
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
- C08L67/06—Unsaturated polyesters
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S525/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S525/911—Polymer from ethylenic monomers only, having terminal functional group other than unsaturation
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S525/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S525/921—Polyester having terminal ethylenic unsaturation other than polyesterurethanes

Landscapes

Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Macromonomer-Based Addition Polymer (AREA)
Graft Or Block Polymers (AREA)
Compositions Of Macromolecular Compounds (AREA)

NO753016A 1974-09-03 1975-09-02 NO753016L (fi)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US05/502,691 US3998909A (en)	1974-09-03	1974-09-03	Molding compounds

Publications (1)

Publication Number	Publication Date
NO753016L true NO753016L (fi)	1976-03-04

Family

ID=23998949

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO753016A NO753016L (fi)	1974-09-03	1975-09-02

Country Status (15)

Country	Link
US (2)	US3998909A (fi)
JP (1)	JPS6016470B2 (fi)
AU (1)	AU504141B2 (fi)
BE (1)	BE832988A (fi)
BR (1)	BR7505578A (fi)
CA (1)	CA1074942A (fi)
DE (1)	DE2535555A1 (fi)
DK (1)	DK393575A (fi)
FI (1)	FI752467A (fi)
FR (1)	FR2283931A1 (fi)
GB (1)	GB1498248A (fi)
IT (1)	IT1048483B (fi)
NL (1)	NL7510148A (fi)
NO (1)	NO753016L (fi)
SE (1)	SE7509613L (fi)

Families Citing this family (18)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
USRE31436E (en) *	1976-04-22	1983-11-01	Phillips Petroleum Company	Thermosetting polyester composition containing normally solid carboxy-containing diene polymer
US4020036A (en) *	1976-04-22	1977-04-26	Phillips Petroleum Company	Thermosetting polyester composition containing normally solid carboxy-containing diene polymer
US4181689A (en) *	1976-09-14	1980-01-01	Idemitsu Kosan Company, Ltd.	Resin compositions containing modified polypropylene
GB1561166A (en) *	1976-10-30	1980-02-13	Idemitsu Kosan Co	Polyolefin resin compositions
US4096107A (en) *	1976-11-12	1978-06-20	Owens-Corning Fiberglas Corporation	Molding compounds
DE2657808C2 (de) *	1976-12-21	1984-05-30	Basf Ag, 6700 Ludwigshafen	Schrumpfarm härtbare Polyesterformmassen und Verfahren zu ihrer Herstellung
DE2903135C2 (de) *	1978-01-30	1983-08-25	Exxon Research and Engineering Co., 07036 Linden, N.J.	Hitzehärtbare Polyesterformmasse, Verfahren zu ihrer Herstellung und ihre Verwendung
US4529757A (en) *	1980-05-16	1985-07-16	The Budd Company	Thermosetting resin patching compound
FR2531092B1 (fr) *	1982-07-27	1985-10-11	Ugine Kuhlmann	Additif antiretrait pour polyester insature, son procede de fabrication, composition antiretrait
US4444921A (en) *	1982-09-24	1984-04-24	Phillips Petroleum Company	Coated calcium carbonate in polyester/rubber molding compound
US4400478A (en) *	1982-12-23	1983-08-23	Shell Oil Company	Molding compounds comprising a mixture of block copolymers employed as a modifier for thermosetting unsaturated polyester resin compositions
DE3332019A1 (de) *	1983-09-06	1985-03-21	Basf Ag, 6700 Ludwigshafen	Haertbare polyesterformmassen
US4737538A (en) *	1985-09-30	1988-04-12	Shell Oil Company	Polymer concrete compositions
US4877832A (en) *	1986-10-29	1989-10-31	Polysar Limited	Thermoset resin compositions
US4978643A (en) *	1987-04-09	1990-12-18	Ceramics Process Systems Corporation	Forming whisker reinforced sintered ceramics with polymerizable binder precursors
US5326516A (en) *	1989-10-03	1994-07-05	Plasticolors, Inc.	Method of preparing a cured pigmented thermosetting polymer composition exhibiting improved color values and reduced haze
US5443775A (en) *	1992-05-08	1995-08-22	Plasticolors, Inc.	Process for preparing pigmented thermoplastic polymer compositions and low shrinking thermosetting resin molding composition
WO2006082595A1 (en) *	2005-02-02	2006-08-10	Defence Research & Development Organisation	Lightweight structural composite for load bearing application

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
BE520039A (fi) *	1950-08-25
IT637063A (fi) *	1960-09-05
BE618066A (fi) *	1961-06-01
FR1413893A (fr) *	1964-05-22	1965-10-15	Pechiney Saint Gobain	Procédé de préparation d'interpolymères du styrène
US3427264A (en) *	1966-02-07	1969-02-11	Exxon Research Engineering Co	Metal-filled plastics comprising a styrene polymer and an elastomer
US3577480A (en) *	1968-11-12	1971-05-04	Hooker Chemical Corp	Graft polymer of a vinyl monomer and a fire retardant polyester
US3857812A (en) *	1969-04-01	1974-12-31	Dow Chemical Co	Unsaturated polyester compositions and thermoset articles prepared therefrom
US3681474A (en) *	1969-09-12	1972-08-01	Richardson Co	Electrical substrates
US3733370A (en) *	1971-05-06	1973-05-15	Atlantic Richfield Co	Unsaturated ester group terminated polydienes as unsaturated polyester modifiers
US3883612A (en) *	1971-06-07	1975-05-13	Scm Corp	Low-shrink thermosetting polymers
US3928494A (en) *	1973-01-09	1975-12-23	Monsanto Co	Polyblend of two types of ABS graft polymers and a copolymer matrix
US3931356A (en) *	1974-04-26	1976-01-06	Monsanto Company	Continuous process for the preparation of ABS type polyblends
US4026969A (en) *	1974-11-15	1977-05-31	Shell Oil Company	Impact improved polymers

1974
- 1974-09-03 US US05/502,691 patent/US3998909A/en not_active Expired - Lifetime
1975
- 1975-07-29 CA CA232,436A patent/CA1074942A/en not_active Expired
- 1975-08-08 DE DE19752535555 patent/DE2535555A1/de not_active Withdrawn
- 1975-08-14 GB GB33942/75A patent/GB1498248A/en not_active Expired
- 1975-08-28 NL NL7510148A patent/NL7510148A/xx not_active Application Discontinuation
- 1975-08-28 AU AU84360/75A patent/AU504141B2/en not_active Expired
- 1975-08-29 SE SE7509613A patent/SE7509613L/xx unknown
- 1975-09-01 BR BR7505578*A patent/BR7505578A/pt unknown
- 1975-09-02 DK DK393575A patent/DK393575A/da unknown
- 1975-09-02 FI FI752467A patent/FI752467A/fi not_active Application Discontinuation
- 1975-09-02 BE BE159672A patent/BE832988A/xx unknown
- 1975-09-02 JP JP50106447A patent/JPS6016470B2/ja not_active Expired
- 1975-09-02 NO NO753016A patent/NO753016L/no unknown
- 1975-09-02 IT IT26817/75A patent/IT1048483B/it active
- 1975-09-02 FR FR7526899A patent/FR2283931A1/fr active Pending
1976
- 1976-09-29 US US05/727,827 patent/US4145381A/en not_active Expired - Lifetime

Also Published As

Publication number	Publication date
BE832988A (fr)	1975-12-31
BR7505578A (pt)	1976-08-03
NL7510148A (nl)	1976-03-05
JPS5152488A (fi)	1976-05-10
SE7509613L (sv)	1976-03-04
FI752467A (fi)	1976-03-04
FR2283931A1 (fr)	1976-04-02
DE2535555A1 (de)	1976-03-11
JPS6016470B2 (ja)	1985-04-25
DK393575A (da)	1976-03-04
GB1498248A (en)	1978-01-18
AU504141B2 (en)	1979-10-04
US3998909A (en)	1976-12-21
US4145381A (en)	1979-03-20
CA1074942A (en)	1980-04-01
AU8436075A (en)	1977-03-03
IT1048483B (it)	1980-11-20

Publication	Publication Date	Title
NO753016L (fi)	1976-03-04
US3110695A (en)	1963-11-12	Process for polymerizing methylmethacrylate in presence of polyethylene oxide
US4075186A (en)	1978-02-21	Graft copolymers of polybutadiene and substituted polyacrylate
US3449471A (en)	1969-06-10	Process for the production of thermoplastic moulding compositions
US3733370A (en)	1973-05-15	Unsaturated ester group terminated polydienes as unsaturated polyester modifiers
US3125546A (en)	1964-03-17	Mechanical properties at various temperatures
US3689596A (en)	1972-09-05	Impact resistant styrene-maleic anhydride/hydroxylated diene block copolymer compositions
US4096107A (en)	1978-06-20	Molding compounds
JPS603327B2 (ja)	1985-01-28	低収縮性不飽和ポリエステル樹脂組成物
US3361845A (en)	1968-01-02	Process for gelling unsaturated polyester resins by addition of alcoholates of aluminum and titanium
US3956421A (en)	1976-05-11	Polar thermoplastic additive for molding compounds and molding compound containing same
US3480598A (en)	1969-11-25	Organic polymeric materials
US4104241A (en)	1978-08-01	Thermosetting additives for polyester-based molding compounds
US4241203A (en)	1980-12-23	Acrylonitrile copolymers having low residual monomer content and methods for their preparation
US3843612A (en)	1974-10-22	Moldable and/or thermoformable acrylic polymers and processes for the production thereof
US4122132A (en)	1978-10-24	Dispersion stabilizer
EP0247257B1 (en)	1993-07-21	Polymer composition containing polycarbonate, a styrenic/maleimide/cyclic anhydride terpolymer and a terpolymer grafted to a polymer matrix
US2628210A (en)	1953-02-10	Oxygenated polymerizable esters as cure accelerators and as copolymerizable materials
US5096966A (en)	1992-03-17	Polymer mixture for flexible sheets
US4552921A (en)	1985-11-12	Method of forming a nonaqueous stable emulsion of rubber in polymerizable monomer, and the polymerization process and thermoplastic copolymer produced thereby
Abdel-azim et al.	1995	Characterization of some aliphatic unsaturated polyesters synthesized for gigantic castings
GB2196011A (en)	1988-04-20	Improvements in the production of graft copolymers
US3794638A (en)	1974-02-26	Thermosetting compositions comprising high vinyl butadiene polymer and a free radical initiator
US4683266A (en)	1987-07-28	Compositions thickened through urethane reaction
Liang et al.	2009	Diallyl orthophthalate as a reactive plasticizer for improving PVC processability, Part III: Curing, properties, and phase separation