NO792982L - Vinylidenkloridpolymerholdig preparat. - Google Patents

Vinylidenkloridpolymerholdig preparat.

Info

Publication number: NO792982L
Authority: NO; Norway
Prior art keywords: vinylidene chloride; latex; preparation according; polymer; ethylenically unsaturated
Prior art date: 1978-09-15

Application number

NO792982A

Other languages

English (en)

Norwegian (no)

Inventor

Dale Sabin Gibbs

Jack Howard Benson

Reet T Fernandez

Original Assignee

Dow Chemical 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.)

1978-09-15

Filing date

1979-09-14

Publication date

1980-03-18

1979-09-14 Application filed by Dow Chemical Co filed Critical Dow Chemical Co

1980-03-18 Publication of NO792982L publication Critical patent/NO792982L/no

Links

229920000642 polymer Polymers 0.000 title claims description 68
238000002360 preparation method Methods 0.000 title claims description 17
LGXVIGDEPROXKC-UHFFFAOYSA-N 1,1-dichloroethene Chemical compound ClC(Cl)=C LGXVIGDEPROXKC-UHFFFAOYSA-N 0.000 title 1
OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 claims description 67
239000000178 monomer Substances 0.000 claims description 39
239000000843 powder Substances 0.000 claims description 37
239000004816 latex Substances 0.000 claims description 32
229920000126 latex Polymers 0.000 claims description 32
239000000203 mixture Substances 0.000 claims description 24
239000002245 particle Substances 0.000 claims description 23
238000000034 method Methods 0.000 claims description 17
238000006116 polymerization reaction Methods 0.000 claims description 16
239000002904 solvent Substances 0.000 claims description 12
230000009466 transformation Effects 0.000 claims description 7
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical group C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims description 6
238000004132 cross linking Methods 0.000 claims description 6
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 4
VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims description 4
125000005907 alkyl ester group Chemical group 0.000 claims description 4
238000007720 emulsion polymerization reaction Methods 0.000 claims description 4
238000000605 extraction Methods 0.000 claims description 3
238000011084 recovery Methods 0.000 claims description 3
GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 claims description 2
150000002825 nitriles Chemical class 0.000 claims description 2
229920002554 vinyl polymer Polymers 0.000 claims description 2
150000001732 carboxylic acid derivatives Chemical class 0.000 claims 1
239000000463 material Substances 0.000 description 38
239000006185 dispersion Substances 0.000 description 23
229920005862 polyol Polymers 0.000 description 20
150000003077 polyols Chemical class 0.000 description 20
229920005830 Polyurethane Foam Polymers 0.000 description 18
239000011496 polyurethane foam Substances 0.000 description 18
238000004519 manufacturing process Methods 0.000 description 17
229920002635 polyurethane Polymers 0.000 description 14
239000004814 polyurethane Substances 0.000 description 14
238000006243 chemical reaction Methods 0.000 description 13
239000003995 emulsifying agent Substances 0.000 description 9
239000006260 foam Substances 0.000 description 7
239000004094 surface-active agent Substances 0.000 description 6
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 5
239000012736 aqueous medium Substances 0.000 description 5
239000001257 hydrogen Substances 0.000 description 5
229910052739 hydrogen Inorganic materials 0.000 description 5
125000002887 hydroxy group Chemical group [H]O* 0.000 description 5
239000007788 liquid Substances 0.000 description 5
239000012948 isocyanate Substances 0.000 description 4
230000000704 physical effect Effects 0.000 description 4
229920000570 polyether Polymers 0.000 description 4
239000000243 solution Substances 0.000 description 4
239000003381 stabilizer Substances 0.000 description 4
JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 3
239000000654 additive Substances 0.000 description 3
230000015572 biosynthetic process Effects 0.000 description 3
239000007795 chemical reaction product Substances 0.000 description 3
239000011248 coating agent Substances 0.000 description 3
238000000576 coating method Methods 0.000 description 3
SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 3
239000006261 foam material Substances 0.000 description 3
150000002513 isocyanates Chemical class 0.000 description 3
-1 methyl methacrylate Chemical compound 0.000 description 3
238000002156 mixing Methods 0.000 description 3
229920000728 polyester Polymers 0.000 description 3
239000000376 reactant Substances 0.000 description 3
MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 2
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
239000004721 Polyphenylene oxide Substances 0.000 description 2
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 2
150000001412 amines Chemical class 0.000 description 2
BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 2
239000003054 catalyst Substances 0.000 description 2
230000015271 coagulation Effects 0.000 description 2
238000005345 coagulation Methods 0.000 description 2
238000002845 discoloration Methods 0.000 description 2
239000000839 emulsion Substances 0.000 description 2
125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 2
229910000041 hydrogen chloride Inorganic materials 0.000 description 2
239000004615 ingredient Substances 0.000 description 2
239000003999 initiator Substances 0.000 description 2
229920001228 polyisocyanate Polymers 0.000 description 2
239000005056 polyisocyanate Substances 0.000 description 2
239000003505 polymerization initiator Substances 0.000 description 2
229920001296 polysiloxane Polymers 0.000 description 2
239000000047 product Substances 0.000 description 2
238000004062 sedimentation Methods 0.000 description 2
238000003756 stirring Methods 0.000 description 2
IMNIMPAHZVJRPE-UHFFFAOYSA-N triethylenediamine Chemical compound C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 description 2
VDYWHVQKENANGY-UHFFFAOYSA-N 1,3-Butyleneglycol dimethacrylate Chemical compound CC(=C)C(=O)OC(C)CCOC(=O)C(C)=C VDYWHVQKENANGY-UHFFFAOYSA-N 0.000 description 1
RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 1
LCPVQAHEFVXVKT-UHFFFAOYSA-N 2-(2,4-difluorophenoxy)pyridin-3-amine Chemical compound NC1=CC=CN=C1OC1=CC=C(F)C=C1F LCPVQAHEFVXVKT-UHFFFAOYSA-N 0.000 description 1
GTEXIOINCJRBIO-UHFFFAOYSA-N 2-[2-(dimethylamino)ethoxy]-n,n-dimethylethanamine Chemical compound CN(C)CCOCCN(C)C GTEXIOINCJRBIO-UHFFFAOYSA-N 0.000 description 1
FQMIAEWUVYWVNB-UHFFFAOYSA-N 3-prop-2-enoyloxybutyl prop-2-enoate Chemical compound C=CC(=O)OC(C)CCOC(=O)C=C FQMIAEWUVYWVNB-UHFFFAOYSA-N 0.000 description 1
XOJWAAUYNWGQAU-UHFFFAOYSA-N 4-(2-methylprop-2-enoyloxy)butyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCCOC(=O)C(C)=C XOJWAAUYNWGQAU-UHFFFAOYSA-N 0.000 description 1
JHWGFJBTMHEZME-UHFFFAOYSA-N 4-prop-2-enoyloxybutyl prop-2-enoate Chemical compound C=CC(=O)OCCCCOC(=O)C=C JHWGFJBTMHEZME-UHFFFAOYSA-N 0.000 description 1
UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
239000004593 Epoxy Substances 0.000 description 1
DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 1
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-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
230000000996 additive effect Effects 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
230000032683 aging Effects 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
125000000217 alkyl group Chemical group 0.000 description 1
125000002947 alkylene group Chemical group 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
150000007514 bases Chemical class 0.000 description 1
239000001110 calcium chloride Substances 0.000 description 1
229910001628 calcium chloride Inorganic materials 0.000 description 1
239000004202 carbamide Substances 0.000 description 1
150000001735 carboxylic acids Chemical class 0.000 description 1
230000015556 catabolic process Effects 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
230000001112 coagulating effect Effects 0.000 description 1
239000000084 colloidal system Substances 0.000 description 1
150000001875 compounds Chemical class 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
229920001577 copolymer Polymers 0.000 description 1
239000003431 cross linking reagent Substances 0.000 description 1
238000000354 decomposition reaction Methods 0.000 description 1
238000006731 degradation reaction Methods 0.000 description 1
ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
239000012153 distilled water Substances 0.000 description 1
238000001035 drying Methods 0.000 description 1
229920001971 elastomer Polymers 0.000 description 1
239000003822 epoxy resin Substances 0.000 description 1
FFYWKOUKJFCBAM-UHFFFAOYSA-N ethenyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC=C FFYWKOUKJFCBAM-UHFFFAOYSA-N 0.000 description 1
BLCTWBJQROOONQ-UHFFFAOYSA-N ethenyl prop-2-enoate Chemical compound C=COC(=O)C=C BLCTWBJQROOONQ-UHFFFAOYSA-N 0.000 description 1
239000003063 flame retardant Substances 0.000 description 1
239000012530 fluid Substances 0.000 description 1
238000005187 foaming Methods 0.000 description 1
LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
239000012760 heat stabilizer Substances 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
150000002596 lactones Chemical class 0.000 description 1
239000004611 light stabiliser Substances 0.000 description 1
230000007774 longterm Effects 0.000 description 1
230000002794 monomerizing effect Effects 0.000 description 1
150000002978 peroxides Chemical class 0.000 description 1
239000002530 phenolic antioxidant Substances 0.000 description 1
239000000049 pigment Substances 0.000 description 1
229920000647 polyepoxide Polymers 0.000 description 1
229920001225 polyester resin Polymers 0.000 description 1
239000004645 polyester resin Substances 0.000 description 1
229920006149 polyester-amide block copolymer Polymers 0.000 description 1
230000000379 polymerizing effect Effects 0.000 description 1
229920005749 polyurethane resin Polymers 0.000 description 1
239000002244 precipitate Substances 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
230000001105 regulatory effect Effects 0.000 description 1
235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
CHQMHPLRPQMAMX-UHFFFAOYSA-L sodium persulfate Substances [Na+].[Na+].[O-]S(=O)(=O)OOS([O-])(=O)=O CHQMHPLRPQMAMX-UHFFFAOYSA-L 0.000 description 1
WVFDILODTFJAPA-UHFFFAOYSA-M sodium;1,4-dihexoxy-1,4-dioxobutane-2-sulfonate Chemical compound [Na+].CCCCCCOC(=O)CC(S([O-])(=O)=O)C(=O)OCCCCCC WVFDILODTFJAPA-UHFFFAOYSA-M 0.000 description 1
238000001694 spray drying Methods 0.000 description 1
235000020354 squash Nutrition 0.000 description 1
238000010561 standard procedure Methods 0.000 description 1
239000007858 starting material Substances 0.000 description 1
239000012747 synergistic agent Substances 0.000 description 1
229920001169 thermoplastic Polymers 0.000 description 1
KSBAEPSJVUENNK-UHFFFAOYSA-L tin(ii) 2-ethylhexanoate Chemical compound [Sn+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O KSBAEPSJVUENNK-UHFFFAOYSA-L 0.000 description 1
DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
150000004072 triols Chemical group 0.000 description 1
238000005406 washing Methods 0.000 description 1
239000002023 wood Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/0061—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof characterized by the use of several polymeric components
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F214/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen
- C08F214/02—Monomers containing chlorine
- C08F214/04—Monomers containing two carbon atoms
- C08F214/08—Vinylidene chloride
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/02—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques
- C08J3/09—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques in organic liquids
- C08J3/11—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques in organic liquids from solid polymers
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2327/00—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Derivatives of such polymers
- C08J2327/02—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Derivatives of such polymers not modified by chemical after-treatment
- C08J2327/04—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Derivatives of such polymers not modified by chemical after-treatment containing chlorine atoms
- C08J2327/08—Homopolymers or copolymers of vinylidene chloride
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2375/00—Characterised by the use of polyureas or polyurethanes; Derivatives of such polymers
- C08J2375/04—Polyurethanes
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2427/00—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Derivatives of such polymers

Landscapes

Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Dispersion Chemistry (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Polyurethanes Or Polyureas (AREA)
Compositions Of Macromolecular Compounds (AREA)
Medicinal Preparation (AREA)

NO792982A 1978-09-15 1979-09-14 Vinylidenkloridpolymerholdig preparat. NO792982L (no)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US94251078A	1978-09-15	1978-09-15

Publications (1)

Publication Number	Publication Date
NO792982L true NO792982L (no)	1980-03-18

Family

ID=25478179

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO792982A NO792982L (no)	1978-09-15	1979-09-14	Vinylidenkloridpolymerholdig preparat.

Country Status (5)

Country	Link
EP (1)	EP0010161A1 (fr)
JP (1)	JPS5540789A (fr)
BR (1)	BR7905887A (fr)
CA (1)	CA1127790A (fr)
NO (1)	NO792982L (fr)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4575529A (en) *	1978-09-15	1986-03-11	The Dow Chemical Company	Dispersible vinylidene chloride polymer powders as additives for polymers
DE3123062A1 (de) *	1981-06-11	1983-02-10	Carsten 3000 Hannover Picker	"geschaeumter, elastischer formkoerper, sowie ein verfahren zu seiner herstellung"

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
NL258390A (fr) *	1959-11-28
GB1025914A (en) *	1963-03-28	1966-04-14	Pittsburgh Plate Glass Co	Polyurethane resin foam
GB1198052A (en) *	1965-02-12	1970-07-08	Ici Ltd	Polymer Dispersions
GB1267905A (en) *	1969-04-28	1972-03-22	Staley Mfg Co A E	Vinylidene chloride copolymer

1979
- 1979-09-14 NO NO792982A patent/NO792982L/no unknown
- 1979-09-14 CA CA335,652A patent/CA1127790A/fr not_active Expired
- 1979-09-14 BR BR7905887A patent/BR7905887A/pt unknown
- 1979-09-14 JP JP11744979A patent/JPS5540789A/ja active Pending
- 1979-09-14 EP EP79103448A patent/EP0010161A1/fr not_active Withdrawn

Also Published As

Publication number	Publication date
CA1127790A (fr)	1982-07-13
EP0010161A1 (fr)	1980-04-30
BR7905887A (pt)	1980-06-03
JPS5540789A (en)	1980-03-22

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JPH06145211A (ja)	1994-05-24	改良された耐燃焼性を有するポリウレタンフォームの製造に有用なポリマー／ポリオール組成物の製造方法
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MXPA98001167A (en)	1998-04-01	Continuous process for the preparation of polimerosde estireno expansi
JPH0457687B2 (fr)	1992-09-14
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US3190847A (en)	1965-06-22	Agglomeration and concentration of synthetic latex
JP2550091B2 (ja)	1996-10-30	重合体／ポリイソシアネート分散体
US4296013A (en)	1981-10-20	Vinylidene chloride polymer microgels
US4273901A (en)	1981-06-16	Dispersible vinylidene chloride polymer microgel powders as additives for polymers
JPH02617A (ja)	1990-01-05	高分子単量体および官能性単量体を用いて製造される安定な低粘度重合体／ポリイソシアネート分散体
US4575529A (en)	1986-03-11	Dispersible vinylidene chloride polymer powders as additives for polymers
CA1127790A (fr)	1982-07-13	Polymeres dispersables en poudre de chlorure de vinylidene, servant d'additifs a des polymeres
NO156570B (no)	1987-07-06	Preparat for anvendelse ved fremstilling av uretanpolymerskum.
US4255306A (en)	1981-03-10	Vinylidene chloride polymer microgels
JPS6336631B2 (fr)	1988-07-21
NO157061B (no)	1987-10-05	Fremgangsmte for fremstilling av et krystallinsk vinylidenkloridpolymerpulver.
US5239008A (en)	1993-08-24	Graft polymerization process using microfluidization in an aqueous emulsion system
KR100195577B1 (ko)	1999-06-15	폴리우레탄 폼 제조용 폴리머/폴리올의 제조방법
JP2000511576A (ja)	2000-09-05	ハロゲン化芳香族モノマー含有ポリマーポリオール及びそれから得られたポリウレタンフォーム
KR100850628B1 (ko)	2008-08-05	복합 나노 입자 및 이의 제조방법
JPS623852B2 (fr)	1987-01-27
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