DK170406B1 - Tværbundet polymersammensætning, en fremgangsmåde til fremstilling deraf og støbte emner fremstillet af polymersammensætningen - Google Patents

Tværbundet polymersammensætning, en fremgangsmåde til fremstilling deraf og støbte emner fremstillet af polymersammensætningen Download PDF

Info

Publication number: DK170406B1
Authority: DK; Denmark
Prior art keywords: weight; terpolymer; composition according; ethylene; mol
Prior art date: 1988-04-18

Application number

DK184989A

Other languages

Danish (da)

English (en)

Other versions

DK184989A (da

DK184989D0 (da

Inventor

Marius Hert

Original Assignee

Norsolor Sa

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.)

1988-04-18

Filing date

1989-04-18

Publication date

1995-08-21

1989-04-18 Application filed by Norsolor Sa filed Critical Norsolor Sa

1989-04-18 Publication of DK184989D0 publication Critical patent/DK184989D0/da

1989-10-19 Publication of DK184989A publication Critical patent/DK184989A/da

1995-08-21 Application granted granted Critical

1995-08-21 Publication of DK170406B1 publication Critical patent/DK170406B1/da

Links

239000000203 mixture Substances 0.000 title claims abstract description 58
238000000034 method Methods 0.000 title claims description 27
229920000642 polymer Polymers 0.000 title claims description 27
229920006037 cross link polymer Polymers 0.000 title description 2
238000002360 preparation method Methods 0.000 title description 2
229920001897 terpolymer Polymers 0.000 claims abstract description 54
229920001155 polypropylene Polymers 0.000 claims abstract description 33
239000003431 cross linking reagent Substances 0.000 claims abstract description 25
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims abstract description 17
239000005977 Ethylene Substances 0.000 claims abstract description 17
229920001577 copolymer Polymers 0.000 claims abstract description 17
150000008064 anhydrides Chemical group 0.000 claims abstract description 16
229920001038 ethylene copolymer Polymers 0.000 claims abstract description 16
125000000217 alkyl group Chemical group 0.000 claims abstract description 11
239000004711 α-olefin Substances 0.000 claims abstract description 6
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims abstract description 5
125000000524 functional group Chemical group 0.000 claims abstract description 5
-1 polyoxypropylene Polymers 0.000 claims description 35
125000004432 carbon atom Chemical group C* 0.000 claims description 13
150000001875 compounds Chemical class 0.000 claims description 11
239000000178 monomer Substances 0.000 claims description 8
238000004898 kneading Methods 0.000 claims description 7
239000004952 Polyamide Substances 0.000 claims description 6
229920002647 polyamide Polymers 0.000 claims description 6
125000003277 amino group Chemical group 0.000 claims description 5
150000002118 epoxides Chemical class 0.000 claims description 5
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims description 5
JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims description 5
229920000647 polyepoxide Polymers 0.000 claims description 5
229920000089 Cyclic olefin copolymer Polymers 0.000 claims description 4
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 4
150000001336 alkenes Chemical class 0.000 claims description 4
150000004985 diamines Chemical class 0.000 claims description 4
125000003700 epoxy group Chemical group 0.000 claims description 4
NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical group NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 claims description 4
239000000155 melt Substances 0.000 claims description 4
229920001451 polypropylene glycol Polymers 0.000 claims description 4
150000003573 thiols Chemical group 0.000 claims description 4
239000004215 Carbon black (E152) Substances 0.000 claims description 3
239000012190 activator Substances 0.000 claims description 3
238000006243 chemical reaction Methods 0.000 claims description 3
239000003795 chemical substances by application Substances 0.000 claims description 3
229930195733 hydrocarbon Natural products 0.000 claims description 3
150000003141 primary amines Chemical class 0.000 claims description 3
150000001252 acrylic acid derivatives Chemical class 0.000 claims description 2
230000003213 activating effect Effects 0.000 claims description 2
239000000654 additive Substances 0.000 claims description 2
239000000945 filler Substances 0.000 claims description 2
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
LGRFSURHDFAFJT-UHFFFAOYSA-N phthalic anhydride Chemical compound C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 claims description 2
OFNISBHGPNMTMS-UHFFFAOYSA-N 3-methylideneoxolane-2,5-dione Chemical compound C=C1CC(=O)OC1=O OFNISBHGPNMTMS-UHFFFAOYSA-N 0.000 claims 1
125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 claims 1
238000004132 cross linking Methods 0.000 abstract description 8
150000001990 dicarboxylic acid derivatives Chemical class 0.000 abstract 1
230000000052 comparative effect Effects 0.000 description 39
239000004743 Polypropylene Substances 0.000 description 21
ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 7
238000005259 measurement Methods 0.000 description 7
235000014113 dietary fatty acids Nutrition 0.000 description 6
239000000194 fatty acid Substances 0.000 description 6
229930195729 fatty acid Natural products 0.000 description 6
150000004665 fatty acids Chemical class 0.000 description 6
239000000956 alloy Substances 0.000 description 5
229910045601 alloy Inorganic materials 0.000 description 5
230000008018 melting Effects 0.000 description 4
238000002844 melting Methods 0.000 description 4
239000003921 oil Substances 0.000 description 4
235000019198 oils Nutrition 0.000 description 4
235000008733 Citrus aurantifolia Nutrition 0.000 description 3
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
235000011941 Tilia x europaea Nutrition 0.000 description 3
CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 3
239000000539 dimer Substances 0.000 description 3
150000002170 ethers Chemical class 0.000 description 3
238000001125 extrusion Methods 0.000 description 3
238000001746 injection moulding Methods 0.000 description 3
239000004571 lime Substances 0.000 description 3
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
LCFVJGUPQDGYKZ-UHFFFAOYSA-N Bisphenol A diglycidyl ether Chemical compound C=1C=C(OCC2OC2)C=CC=1C(C)(C)C(C=C1)=CC=C1OCC1CO1 LCFVJGUPQDGYKZ-UHFFFAOYSA-N 0.000 description 2
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 2
125000001931 aliphatic group Chemical group 0.000 description 2
125000005250 alkyl acrylate group Chemical group 0.000 description 2
150000001412 amines Chemical class 0.000 description 2
IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical class C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 2
229910052799 carbon Inorganic materials 0.000 description 2
GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical class C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 2
150000002009 diols Chemical class 0.000 description 2
VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 description 2
238000002347 injection Methods 0.000 description 2
239000007924 injection Substances 0.000 description 2
239000000463 material Substances 0.000 description 2
PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 2
230000035699 permeability Effects 0.000 description 2
239000004014 plasticizer Substances 0.000 description 2
239000007921 spray Substances 0.000 description 2
150000003512 tertiary amines Chemical class 0.000 description 2
RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 2
YIWGJFPJRAEKMK-UHFFFAOYSA-N 1-(2H-benzotriazol-5-yl)-3-methyl-8-[2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carbonyl]-1,3,8-triazaspiro[4.5]decane-2,4-dione Chemical group CN1C(=O)N(c2ccc3n[nH]nc3c2)C2(CCN(CC2)C(=O)c2cnc(NCc3cccc(OC(F)(F)F)c3)nc2)C1=O YIWGJFPJRAEKMK-UHFFFAOYSA-N 0.000 description 1
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 1
GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 1
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
SYEWHONLFGZGLK-UHFFFAOYSA-N 2-[1,3-bis(oxiran-2-ylmethoxy)propan-2-yloxymethyl]oxirane Chemical compound C1OC1COCC(OCC1OC1)COCC1CO1 SYEWHONLFGZGLK-UHFFFAOYSA-N 0.000 description 1
PLDLPVSQYMQDBL-UHFFFAOYSA-N 2-[[3-(oxiran-2-ylmethoxy)-2,2-bis(oxiran-2-ylmethoxymethyl)propoxy]methyl]oxirane Chemical compound C1OC1COCC(COCC1OC1)(COCC1OC1)COCC1CO1 PLDLPVSQYMQDBL-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
CFVWNXQPGQOHRJ-UHFFFAOYSA-N 2-methylpropyl prop-2-enoate Chemical compound CC(C)COC(=O)C=C CFVWNXQPGQOHRJ-UHFFFAOYSA-N 0.000 description 1
MECNWXGGNCJFQJ-UHFFFAOYSA-N 3-piperidin-1-ylpropane-1,2-diol Chemical compound OCC(O)CN1CCCCC1 MECNWXGGNCJFQJ-UHFFFAOYSA-N 0.000 description 1
239000005995 Aluminium silicate Substances 0.000 description 1
239000004593 Epoxy Substances 0.000 description 1
241000282320 Panthera leo Species 0.000 description 1
229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
KZTYYGOKRVBIMI-UHFFFAOYSA-N S-phenyl benzenesulfonothioate Natural products C=1C=CC=CC=1S(=O)(=O)C1=CC=CC=C1 KZTYYGOKRVBIMI-UHFFFAOYSA-N 0.000 description 1
235000012211 aluminium silicate Nutrition 0.000 description 1
239000010692 aromatic oil Substances 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
238000009529 body temperature measurement Methods 0.000 description 1
CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 1
239000006229 carbon black Substances 0.000 description 1
235000019241 carbon black Nutrition 0.000 description 1
238000010382 chemical cross-linking Methods 0.000 description 1
239000011248 coating agent Substances 0.000 description 1
238000000576 coating method Methods 0.000 description 1
239000012990 dithiocarbamate Substances 0.000 description 1
238000006735 epoxidation reaction Methods 0.000 description 1
239000003822 epoxy resin Substances 0.000 description 1
CGPRUXZTHGTMKW-UHFFFAOYSA-N ethene;ethyl prop-2-enoate Chemical compound C=C.CCOC(=O)C=C CGPRUXZTHGTMKW-UHFFFAOYSA-N 0.000 description 1
HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 description 1
229920005676 ethylene-propylene block copolymer Polymers 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
238000010101 extrusion blow moulding Methods 0.000 description 1
239000008187 granular material Substances 0.000 description 1
239000008202 granule composition Substances 0.000 description 1
229920001519 homopolymer Polymers 0.000 description 1
239000011256 inorganic filler Substances 0.000 description 1
229910003475 inorganic filler Inorganic materials 0.000 description 1
125000003010 ionic group Chemical group 0.000 description 1
NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
239000007788 liquid Substances 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
239000011159 matrix material Substances 0.000 description 1
239000012528 membrane Substances 0.000 description 1
XLSZMDLNRCVEIJ-UHFFFAOYSA-N methylimidazole Natural products CC1=CNC=N1 XLSZMDLNRCVEIJ-UHFFFAOYSA-N 0.000 description 1
239000010445 mica Substances 0.000 description 1
229910052618 mica group Inorganic materials 0.000 description 1
SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
RPQRDASANLAFCM-UHFFFAOYSA-N oxiran-2-ylmethyl prop-2-enoate Chemical compound C=CC(=O)OCC1CO1 RPQRDASANLAFCM-UHFFFAOYSA-N 0.000 description 1
239000012188 paraffin wax Substances 0.000 description 1
239000011236 particulate material Substances 0.000 description 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
230000000750 progressive effect Effects 0.000 description 1
230000001737 promoting effect Effects 0.000 description 1
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
229920001384 propylene homopolymer Polymers 0.000 description 1
238000005086 pumping Methods 0.000 description 1
150000003242 quaternary ammonium salts Chemical class 0.000 description 1
229920005989 resin Polymers 0.000 description 1
239000011347 resin Substances 0.000 description 1
150000003335 secondary amines Chemical group 0.000 description 1
239000002904 solvent Substances 0.000 description 1
235000012424 soybean oil Nutrition 0.000 description 1
239000003549 soybean oil Substances 0.000 description 1
150000005846 sugar alcohols Polymers 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
235000012222 talc Nutrition 0.000 description 1
150000004072 triols Chemical class 0.000 description 1
239000011701 zinc Substances 0.000 description 1
229910052725 zinc Inorganic materials 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
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/04—Homopolymers or copolymers of ethene
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L51/00—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
- C08L51/06—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers grafted on to homopolymers or copolymers of aliphatic hydrocarbons containing only one carbon-to-carbon double bond
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/04—Homopolymers or copolymers of ethene
- C08L23/08—Copolymers of ethene
- C08L23/0846—Copolymers of ethene with unsaturated hydrocarbons containing atoms other than carbon or hydrogen
- C08L23/0869—Copolymers of ethene with unsaturated hydrocarbons containing atoms other than carbon or hydrogen with unsaturated acids, e.g. [meth]acrylic acid; with unsaturated esters, e.g. [meth]acrylic acid esters
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/10—Homopolymers or copolymers of propene
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/10—Homopolymers or copolymers of propene
- C08L23/12—Polypropene
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/10—Homopolymers or copolymers of propene
- C08L23/14—Copolymers of propene
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/02—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/03—Polymer mixtures characterised by other features containing three or more polymers in a blend
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2312/00—Crosslinking

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Chemical & Material Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Compositions Of Macromolecular Compounds (AREA)
Processes Of Treating Macromolecular Substances (AREA)
Graft Or Block Polymers (AREA)
Manufacture Of Macromolecular Shaped Articles (AREA)
Medicinal Preparation (AREA)
Epoxy Resins (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

DK184989A 1988-04-18 1989-04-18 Tværbundet polymersammensætning, en fremgangsmåde til fremstilling deraf og støbte emner fremstillet af polymersammensætningen DK170406B1 (da)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
FR8805066A FR2630123B1 (fr)	1988-04-18	1988-04-18	Compositions polymeres reticulees, leur procede de fabrication et articles moules obtenus
FR8805066		1988-04-18

Publications (3)

Publication Number	Publication Date
DK184989D0 DK184989D0 (da)	1989-04-18
DK184989A DK184989A (da)	1989-10-19
DK170406B1 true DK170406B1 (da)	1995-08-21

Family

ID=9365378

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DK184989A DK170406B1 (da)	1988-04-18	1989-04-18	Tværbundet polymersammensætning, en fremgangsmåde til fremstilling deraf og støbte emner fremstillet af polymersammensætningen

Country Status (20)

Country	Link
US (1)	US4990566A (sv)
EP (1)	EP0343024B1 (sv)
JP (1)	JPH0819299B2 (sv)
KR (1)	KR890016106A (sv)
CN (1)	CN1038824A (sv)
AT (1)	ATE83496T1 (sv)
AU (1)	AU607064B2 (sv)
BR (1)	BR8901855A (sv)
CA (1)	CA1331658C (sv)
DE (1)	DE68903877T2 (sv)
DK (1)	DK170406B1 (sv)
ES (1)	ES2054046T3 (sv)
FI (1)	FI98523C (sv)
FR (1)	FR2630123B1 (sv)
GR (1)	GR3007010T3 (sv)
MX (1)	MX171237B (sv)
NO (1)	NO178971C (sv)
NZ (1)	NZ228556A (sv)
PT (1)	PT90278B (sv)
ZA (1)	ZA892445B (sv)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US5037888A (en) *	1989-11-09	1991-08-06	Eastman Kodak Company	Thermoplastic elastomeric compositions and method for their preparation
FR2656321B1 (fr) *	1989-12-27	1992-03-27	Norsolor Sa	Compositions comprenant des copolymeres d'ethylene.
FI97143C (sv) *	1991-12-30	1996-10-25	Borealis As	Dynamiskt tvärbunden polyolefinblandning
US6194113B1 (en) *	1997-06-27	2001-02-27	Tomoegawa Paper Co., Ltd.	Olefinic resin and electrophotographic toner prepared therefrom
JP4036516B2 (ja) *	1997-12-05	2008-01-23	株式会社巴川製紙所	電子写真用トナー
US6777046B1 (en)	1998-07-07	2004-08-17	Curwood, Inc.	Puncture resistant, high shrink films, blends, and process
US6864195B2 (en) *	2002-08-15	2005-03-08	Bfs Diversified Products, Llc	Heat weldable roofing membrane
US7101628B2 (en) *	2003-03-20	2006-09-05	Bfs Diversified Products, Llc	Thermoplastic vulcanizate and membrane for covering a roof made therefrom
CA2735125C (en) *	2008-08-25	2016-09-27	Dow Global Technologies Llc	Method of crosslinking carboxyl-containing polymers using oligoamines
WO2012010453A1 (en)	2010-07-19	2012-01-26	Dsm Ip Assets B.V.	Flame retardant insulated electrical wire
CN107001524B (zh) *	2014-12-15	2020-11-17	住友化学株式会社	聚合物
JP6877425B2 (ja)	2016-06-15	2021-05-26	住友化学株式会社	重合体、成形体、発泡体、樹脂組成物および重合体の製造方法
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FR2554112B1 (fr) *	1983-10-28	1986-05-16	Charbonnages Ste Chimique	Procede de reticulation de polymeres d'ethylene contenant des fonctions anhydride, compositions polymeres reticulables et application de ces compositions a l'enduction de substrats
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1988
- 1988-04-18 FR FR8805066A patent/FR2630123B1/fr not_active Expired - Fee Related
1989
- 1989-03-31 NZ NZ228556A patent/NZ228556A/xx unknown
- 1989-04-03 ZA ZA892445A patent/ZA892445B/xx unknown
- 1989-04-14 PT PT90278A patent/PT90278B/pt active IP Right Grant
- 1989-04-14 NO NO891539A patent/NO178971C/no unknown
- 1989-04-14 BR BR898901855A patent/BR8901855A/pt not_active Application Discontinuation
- 1989-04-17 ES ES89401051T patent/ES2054046T3/es not_active Expired - Lifetime
- 1989-04-17 DE DE8989401051T patent/DE68903877T2/de not_active Expired - Fee Related
- 1989-04-17 FI FI891810A patent/FI98523C/sv not_active IP Right Cessation
- 1989-04-17 AT AT89401051T patent/ATE83496T1/de not_active IP Right Cessation
- 1989-04-17 EP EP89401051A patent/EP0343024B1/fr not_active Expired - Lifetime
- 1989-04-17 US US07/338,662 patent/US4990566A/en not_active Expired - Fee Related
- 1989-04-18 AU AU33099/89A patent/AU607064B2/en not_active Ceased
- 1989-04-18 MX MX015691A patent/MX171237B/es unknown
- 1989-04-18 JP JP1098662A patent/JPH0819299B2/ja not_active Expired - Lifetime
- 1989-04-18 CN CN89103680A patent/CN1038824A/zh active Pending
- 1989-04-18 DK DK184989A patent/DK170406B1/da not_active IP Right Cessation
- 1989-04-18 CA CA000597016A patent/CA1331658C/fr not_active Expired - Fee Related
- 1989-04-18 KR KR1019890005111A patent/KR890016106A/ko not_active Withdrawn
1993
- 1993-02-10 GR GR930400250T patent/GR3007010T3/el unknown

Also Published As

Publication number	Publication date
BR8901855A (pt)	1989-11-28
ZA892445B (en)	1989-12-27
US4990566A (en)	1991-02-05
JPH0819299B2 (ja)	1996-02-28
ES2054046T3 (es)	1994-08-01
AU607064B2 (en)	1991-02-21
DE68903877D1 (de)	1993-01-28
FI98523B (sv)	1997-03-27
CN1038824A (zh)	1990-01-17
PT90278A (pt)	1989-11-10
FI891810A0 (sv)	1989-04-17
DK184989A (da)	1989-10-19
DE68903877T2 (de)	1993-05-19
ATE83496T1 (de)	1993-01-15
AU3309989A (en)	1989-10-19
NZ228556A (en)	1990-10-26
DK184989D0 (da)	1989-04-18
PT90278B (pt)	1994-07-29
CA1331658C (fr)	1994-08-23
NO891539L (no)	1989-10-19
FI891810L (sv)	1989-10-19
FR2630123B1 (fr)	1992-02-21
GR3007010T3 (sv)	1993-07-30
NO178971B (no)	1996-04-01
EP0343024A1 (fr)	1989-11-23
FI98523C (sv)	1997-07-10
MX171237B (es)	1993-10-13
FR2630123A1 (fr)	1989-10-20
EP0343024B1 (fr)	1992-12-16
NO891539D0 (no)	1989-04-14
KR890016106A (ko)	1989-11-28
JPH01311145A (ja)	1989-12-15
NO178971C (no)	1996-07-10

Publication	Publication Date	Title
DK170406B1 (da)	1995-08-21	Tværbundet polymersammensætning, en fremgangsmåde til fremstilling deraf og støbte emner fremstillet af polymersammensætningen
CA1335131C (en)	1995-04-04	Thermoplastic resin composition
KR890002431B1 (ko)	1989-07-03	혼화성을 갖는 아크릴 에스테르 공중합체 고무의 블렌드
KR910000942B1 (ko)	1991-02-19	폴리올레핀 및 에틸렌 함량이 높은 에틸렌/알킬 아크릴레이트 탄성중합체의 열가소성 조성물과 그 제조방법
EP0247580A2 (en)	1987-12-02	Thermoplastic composition of crystalline polyolefin and ethylene-containing copolymer
JPH10505615A (ja)	1998-06-02	油膨脹及び圧縮永久歪みへの改良された耐性を有する軟質熱可塑性エラストマー
KR20000064725A (ko)	2000-11-06	일액형상온습기경화성수지조성물
CA1335132C (en)	1995-04-04	Process for producing impact resistant polyamide resin composition
US4624989A (en)	1986-11-25	Thermoplastic elastomers containing cross-linked epihalohydrin rubbers
JPH07258540A (ja)	1995-10-09	エポキシド基を有するエチレンポリマーを含むポリアミド樹脂をベースとした多相熱可塑性組成物
AU586617B2 (en)	1989-07-20	Polymer blends containing a polymer having pendant oxazoline groups
GB2284211A (en)	1995-05-31	Polyphenylene sulphide-based compositions with improved impact strength and process for preparing them
US5091469A (en)	1992-02-25	Compatibilized epoxy/polyamide compositions containing polyolefins
GB2197654A (en)	1988-05-25	Thermoplastic compositions
JPH0354989B2 (sv)	1991-08-21
JPH0354990B2 (sv)	1991-08-21
JPH05331321A (ja)	1993-12-14	動的架橋されたポリオレフィン類
US5208290A (en)	1993-05-04	Epoxy resin crosslinked with polyamine and chlorosulfonated polyolefin
US4654402A (en)	1987-03-31	Graft polymer of acrylic ester rubber and polyolefin
JPH05239350A (ja)	1993-09-17	改良された衝撃強さをもつポリフェニレンスルフィドを主成分とする組成物およびその製造方法
JPS62172056A (ja)	1987-07-29	ポリフエニレンスルフイド組成物
JPS58198501A (ja)	1983-11-18	変性ポリオレフイン架橋物の製造方法
EP0633910A1 (en)	1995-01-18	Polymer composition comprising a mixture of a crystalline or semi-crystalline polyolefin and a polymer based on vinylaromatic and dicarboxylic acid anhydride monomer units
CA1322618C (en)	1993-09-28	Compatibilized blends of acrylic ester copolymer rubber
JPH05214224A (ja)	1993-08-24	熱可塑性樹脂組成物

Legal Events

Date	Code	Title	Description
1995-08-21	B1	Patent granted (law 1993)
1999-03-15	PBP	Patent lapsed