DD283636A5 - Elastoplastische zusammensetungen und verfahren zu deren herstellungen - Google Patents
Elastoplastische zusammensetungen und verfahren zu deren herstellungen Download PDFInfo
- Publication number
- DD283636A5 DD283636A5 DD88322933A DD32293388A DD283636A5 DD 283636 A5 DD283636 A5 DD 283636A5 DD 88322933 A DD88322933 A DD 88322933A DD 32293388 A DD32293388 A DD 32293388A DD 283636 A5 DD283636 A5 DD 283636A5
- Authority
- DD
- German Democratic Republic
- Prior art keywords
- compositions
- epdm rubber
- styrene
- polyolefin
- rubber
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 83
- 238000000034 method Methods 0.000 title claims abstract description 9
- 238000004519 manufacturing process Methods 0.000 title claims description 6
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims abstract description 58
- 229920002943 EPDM rubber Polymers 0.000 claims abstract description 41
- 229920000098 polyolefin Polymers 0.000 claims abstract description 33
- 229920000642 polymer Polymers 0.000 claims abstract description 30
- 238000004132 cross linking Methods 0.000 claims abstract description 19
- 229920001971 elastomer Polymers 0.000 claims abstract description 16
- 229920001169 thermoplastic Polymers 0.000 claims abstract description 16
- 239000004416 thermosoftening plastic Substances 0.000 claims abstract description 16
- 239000005060 rubber Substances 0.000 claims abstract description 15
- 239000002245 particle Substances 0.000 claims abstract description 11
- 150000001993 dienes Chemical class 0.000 claims abstract description 6
- 239000004711 α-olefin Substances 0.000 claims abstract description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 5
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims abstract description 4
- 239000005977 Ethylene Substances 0.000 claims abstract description 4
- 229920005672 polyolefin resin Polymers 0.000 claims abstract description 4
- 229920005606 polypropylene copolymer Polymers 0.000 claims abstract description 4
- 239000004793 Polystyrene Substances 0.000 claims description 20
- 239000004743 Polypropylene Substances 0.000 claims description 19
- 229920001155 polypropylene Polymers 0.000 claims description 19
- 229920002223 polystyrene Polymers 0.000 claims description 16
- -1 polypropylene Polymers 0.000 claims description 10
- 229920001577 copolymer Polymers 0.000 claims description 8
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical class [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 claims description 6
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims description 6
- 239000004606 Fillers/Extenders Substances 0.000 claims description 6
- 239000008240 homogeneous mixture Substances 0.000 claims description 4
- 239000012764 mineral filler Substances 0.000 claims description 2
- 229920006132 styrene block copolymer Polymers 0.000 claims description 2
- 238000002360 preparation method Methods 0.000 abstract description 6
- 239000000956 alloy Substances 0.000 description 34
- 229910045601 alloy Inorganic materials 0.000 description 34
- 239000003921 oil Substances 0.000 description 12
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 10
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 8
- 229920005669 high impact polystyrene Polymers 0.000 description 7
- 239000004797 high-impact polystyrene Substances 0.000 description 7
- 230000006835 compression Effects 0.000 description 6
- 238000007906 compression Methods 0.000 description 6
- 229920000578 graft copolymer Polymers 0.000 description 6
- 238000002156 mixing Methods 0.000 description 6
- 239000011787 zinc oxide Substances 0.000 description 5
- 239000000178 monomer Substances 0.000 description 4
- 229920001568 phenolic resin Polymers 0.000 description 4
- 239000005011 phenolic resin Substances 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- 239000004971 Cross linker Substances 0.000 description 3
- 229920001400 block copolymer Polymers 0.000 description 3
- 238000000265 homogenisation Methods 0.000 description 3
- YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 description 3
- 150000002978 peroxides Chemical class 0.000 description 3
- 230000008569 process Effects 0.000 description 3
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 2
- 239000012190 activator Substances 0.000 description 2
- 150000001336 alkenes Chemical class 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical class C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 238000010077 mastication Methods 0.000 description 2
- 230000018984 mastication Effects 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 229920003048 styrene butadiene rubber Polymers 0.000 description 2
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 2
- 230000008719 thickening Effects 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- JBVMSEMQJGGOFR-FNORWQNLSA-N (4e)-4-methylhexa-1,4-diene Chemical compound C\C=C(/C)CC=C JBVMSEMQJGGOFR-FNORWQNLSA-N 0.000 description 1
- TVEFFNLPYIEDLS-VQHVLOKHSA-N (4e)-deca-1,4,9-triene Chemical compound C=CCCC\C=C\CC=C TVEFFNLPYIEDLS-VQHVLOKHSA-N 0.000 description 1
- PRBHEGAFLDMLAL-GQCTYLIASA-N (4e)-hexa-1,4-diene Chemical compound C\C=C\CC=C PRBHEGAFLDMLAL-GQCTYLIASA-N 0.000 description 1
- OJOWICOBYCXEKR-KRXBUXKQSA-N (5e)-5-ethylidenebicyclo[2.2.1]hept-2-ene Chemical compound C1C2C(=C/C)/CC1C=C2 OJOWICOBYCXEKR-KRXBUXKQSA-N 0.000 description 1
- RCJMVGJKROQDCB-UHFFFAOYSA-N 1,3-dimethyl-1,3-butadiene Natural products CC=CC(C)=C RCJMVGJKROQDCB-UHFFFAOYSA-N 0.000 description 1
- VYXHVRARDIDEHS-UHFFFAOYSA-N 1,5-cyclooctadiene Chemical compound C1CC=CCCC=C1 VYXHVRARDIDEHS-UHFFFAOYSA-N 0.000 description 1
- 239000004912 1,5-cyclooctadiene Substances 0.000 description 1
- QXQAPNSHUJORMC-UHFFFAOYSA-N 1-chloro-4-propylbenzene Chemical compound CCCC1=CC=C(Cl)C=C1 QXQAPNSHUJORMC-UHFFFAOYSA-N 0.000 description 1
- HECLRDQVFMWTQS-RGOKHQFPSA-N 1755-01-7 Chemical compound C1[C@H]2[C@@H]3CC=C[C@@H]3[C@@H]1C=C2 HECLRDQVFMWTQS-RGOKHQFPSA-N 0.000 description 1
- RAXXELZNTBOGNW-UHFFFAOYSA-N 1H-imidazole Chemical compound C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 1
- FXNDIJDIPNCZQJ-UHFFFAOYSA-N 2,4,4-trimethylpent-1-ene Chemical compound CC(=C)CC(C)(C)C FXNDIJDIPNCZQJ-UHFFFAOYSA-N 0.000 description 1
- DRWYRROCDFQZQF-UHFFFAOYSA-N 2-methylpenta-1,4-diene Chemical compound CC(=C)CC=C DRWYRROCDFQZQF-UHFFFAOYSA-N 0.000 description 1
- PKXHXOTZMFCXSH-UHFFFAOYSA-N 3,3-dimethylbut-1-ene Chemical compound CC(C)(C)C=C PKXHXOTZMFCXSH-UHFFFAOYSA-N 0.000 description 1
- RITONZMLZWYPHW-UHFFFAOYSA-N 3-methylhex-1-ene Chemical compound CCCC(C)C=C RITONZMLZWYPHW-UHFFFAOYSA-N 0.000 description 1
- WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 description 1
- VSQLAQKFRFTMNS-UHFFFAOYSA-N 5-methylhexa-1,4-diene Chemical compound CC(C)=CCC=C VSQLAQKFRFTMNS-UHFFFAOYSA-N 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
- 229920000181 Ethylene propylene rubber Polymers 0.000 description 1
- 229920002633 Kraton (polymer) Polymers 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- YGSDEFSMJLZEOE-UHFFFAOYSA-N Salicylic acid Natural products OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical class [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 229920001871 amorphous plastic Polymers 0.000 description 1
- 229920006125 amorphous polymer Polymers 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- XRERONKQLIQWGW-UHFFFAOYSA-N but-1-ene;styrene Chemical compound CCC=C.C=CC1=CC=CC=C1 XRERONKQLIQWGW-UHFFFAOYSA-N 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- GDVKFRBCXAPAQJ-UHFFFAOYSA-A dialuminum;hexamagnesium;carbonate;hexadecahydroxide Chemical compound [OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Al+3].[Al+3].[O-]C([O-])=O GDVKFRBCXAPAQJ-UHFFFAOYSA-A 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 229920013728 elastomeric terpolymer Polymers 0.000 description 1
- 238000001493 electron microscopy Methods 0.000 description 1
- BXOUVIIITJXIKB-UHFFFAOYSA-N ethene;styrene Chemical group C=C.C=CC1=CC=CC=C1 BXOUVIIITJXIKB-UHFFFAOYSA-N 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 238000009778 extrusion testing Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000007970 homogeneous dispersion Substances 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 229910001701 hydrotalcite Inorganic materials 0.000 description 1
- 229960001545 hydrotalcite Drugs 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 239000011872 intimate mixture Substances 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 1
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- DYUMLJSJISTVPV-UHFFFAOYSA-N phenyl propanoate Chemical compound CCC(=O)OC1=CC=CC=C1 DYUMLJSJISTVPV-UHFFFAOYSA-N 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920002285 poly(styrene-co-acrylonitrile) Polymers 0.000 description 1
- 229920001083 polybutene Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- YARNEMCKJLFQHG-UHFFFAOYSA-N prop-1-ene;styrene Chemical group CC=C.C=CC1=CC=CC=C1 YARNEMCKJLFQHG-UHFFFAOYSA-N 0.000 description 1
- SCUZVMOVTVSBLE-UHFFFAOYSA-N prop-2-enenitrile;styrene Chemical compound C=CC#N.C=CC1=CC=CC=C1 SCUZVMOVTVSBLE-UHFFFAOYSA-N 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 230000000707 stereoselective effect Effects 0.000 description 1
- 229920000638 styrene acrylonitrile Polymers 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
- 229920001897 terpolymer Polymers 0.000 description 1
- OPQYOFWUFGEMRZ-UHFFFAOYSA-N tert-butyl 2,2-dimethylpropaneperoxoate Chemical compound CC(C)(C)OOC(=O)C(C)(C)C OPQYOFWUFGEMRZ-UHFFFAOYSA-N 0.000 description 1
- 238000004073 vulcanization Methods 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
-
- 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
- C08L23/16—Elastomeric ethene-propene or ethene-propene-diene copolymers, e.g. EPR and EPDM rubbers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L25/00—Compositions 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 an aromatic carbocyclic ring; Compositions of derivatives of such polymers
- C08L25/02—Homopolymers or copolymers of hydrocarbons
- C08L25/04—Homopolymers or copolymers of styrene
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
- Silicates, Zeolites, And Molecular Sieves (AREA)
- Compositions Of Oxide Ceramics (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Materials For Medical Uses (AREA)
- Medicinal Preparation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Mushroom Cultivation (AREA)
- Processing Of Solid Wastes (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT22946/87A IT1223262B (it) | 1987-12-11 | 1987-12-11 | Composizioni elasto plastiche e procedimento per la loro preparazione |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DD283636A5 true DD283636A5 (de) | 1990-10-17 |
Family
ID=11202174
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DD88322933A DD283636A5 (de) | 1987-12-11 | 1988-12-09 | Elastoplastische zusammensetungen und verfahren zu deren herstellungen |
Country Status (20)
| Country | Link |
|---|---|
| US (1) | US4889888A (ru) |
| EP (1) | EP0320001B2 (ru) |
| JP (1) | JP2716487B2 (ru) |
| KR (1) | KR0139092B1 (ru) |
| CN (1) | CN1035950C (ru) |
| AT (1) | ATE107680T1 (ru) |
| AU (1) | AU615697B2 (ru) |
| BR (1) | BR8806525A (ru) |
| CA (1) | CA1334549C (ru) |
| CZ (1) | CZ277978B6 (ru) |
| DD (1) | DD283636A5 (ru) |
| DE (1) | DE3850365T3 (ru) |
| DK (1) | DK686588A (ru) |
| ES (1) | ES2055731T5 (ru) |
| IT (1) | IT1223262B (ru) |
| MX (1) | MX14084A (ru) |
| NO (1) | NO885477L (ru) |
| PT (1) | PT89189B (ru) |
| RU (1) | RU2074868C1 (ru) |
| ZA (1) | ZA889209B (ru) |
Families Citing this family (27)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3039560B2 (ja) * | 1989-12-27 | 2000-05-08 | 日本石油化学株式会社 | 熱可塑性樹脂組成物およびその用途 |
| JPH03203943A (ja) * | 1989-12-28 | 1991-09-05 | Nippon Petrochem Co Ltd | 熱可塑性樹脂組成物 |
| DE4211416C3 (de) * | 1992-04-04 | 2000-07-13 | Benecke Ag J H | Folie oder Formkörper aus einem thermoplastischen Kunststoff mit einem Terpolymergehalt sowie deren Verwendung |
| CA2127575C (en) * | 1993-07-08 | 1999-07-06 | Yuichi Itoh | Olefin thermoplastic elastomer and laminate thereof |
| US5378760A (en) * | 1993-11-10 | 1995-01-03 | Shell Oil Company | Blends of polystyrene/polypropylene grafted polymers and elastomeric tetrablock copolymers |
| TW440585B (en) * | 1995-07-05 | 2001-06-16 | Mitsui Chemicals Inc | A rubber composition and its production method |
| EP0757077A1 (en) | 1995-08-01 | 1997-02-05 | Advanced Elastomer Systems, L.P. | Very soft thermoplastic elastomer compositions |
| AU1946597A (en) * | 1996-04-12 | 1997-11-07 | Dsm N.V. | Thermoplastic elastomer |
| US5932342A (en) * | 1996-11-14 | 1999-08-03 | Nashua Corporation | Optical diffusers obtained by fluid phase mixing of incompatible materials |
| US5939464A (en) * | 1997-05-02 | 1999-08-17 | Advanced Elastomer Systems, L.P. | High elasticity foams |
| DE19832074A1 (de) * | 1997-07-17 | 1999-01-21 | Sumitomo Chemical Co | Airbag-Abdeckung für einen Beifahrer in einem Kraftfahrzeug |
| DE69915900T3 (de) † | 1998-01-20 | 2008-06-26 | Jsr Corp. | Thermoplastische Elastomerzusammensetzung |
| JP4238480B2 (ja) * | 1998-05-07 | 2009-03-18 | チッソ株式会社 | ポリプロピレン系成形品 |
| US6476132B1 (en) * | 1999-07-23 | 2002-11-05 | Advanced Elastomer Systems, L.P. | Use of a silane grafted polyolefin in EPDM/polyolefin thermoplastic vulcanizates to improve compression set |
| JP2001072815A (ja) | 1999-09-07 | 2001-03-21 | Chisso Corp | プロピレン系樹脂組成物 |
| EP1243615B1 (en) * | 1999-12-27 | 2007-11-28 | Asahi Kasei Kabushiki Kaisha | Thermoplastic crosslinked rubber compositions |
| KR20020071977A (ko) * | 2000-01-31 | 2002-09-13 | 어드밴스드 엘라스토머 시스템즈,엘.피. | 개선된 접착 특성을 가지는 열가소성 탄성중합체 |
| CN1171945C (zh) * | 2000-03-02 | 2004-10-20 | 旭化成株式会社 | 热塑性弹性体组合物 |
| JP2002018887A (ja) | 2000-07-12 | 2002-01-22 | Chisso Corp | ポリプロピレン樹脂発泡成形体 |
| US6780937B2 (en) * | 2002-08-29 | 2004-08-24 | The Goodyear Tire & Rubber Company | Emulsion particles as reinforcing fillers |
| KR100632603B1 (ko) * | 2003-08-20 | 2006-10-09 | 에스케이 주식회사 | 열가소성 에라스토머 조성물 및 이의 제조방법 |
| US7439304B2 (en) * | 2004-06-03 | 2008-10-21 | Advanced Elastomer Systems, L.P. | Thermoplastic vulcanizates and process for making the same |
| ITVR20040074A1 (it) * | 2004-05-03 | 2004-08-03 | So F Ter S P A | Composizioni plasto-elastomeriche a base di poliolefine e terpolimeri epdm addizionate di cariche minerali. |
| JP4436194B2 (ja) * | 2004-06-18 | 2010-03-24 | リケンテクノス株式会社 | 熱可塑性エラストマー組成物 |
| US8653170B2 (en) * | 2005-06-27 | 2014-02-18 | Exxonmobil Chemical Patents Inc. | Dynamic vulcanization process for preparing thermoplastic elastomers |
| US7655728B2 (en) * | 2005-06-27 | 2010-02-02 | Exxonmobil Chemical Patents Inc. | Preparation of thermoplastic elastomers by dynamic vulcanization in multi-screw extruders |
| CN103183870B (zh) * | 2011-12-29 | 2016-09-07 | 合肥杰事杰新材料股份有限公司 | 一种聚烯烃/苯乙烯基树脂组合物及其制备方法 |
Family Cites Families (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3806558A (en) * | 1971-08-12 | 1974-04-23 | Uniroyal Inc | Dynamically partially cured thermoplastic blend of monoolefin copolymer rubber and polyolefin plastic |
| US4311628A (en) * | 1977-11-09 | 1982-01-19 | Monsanto Company | Thermoplastic elastomeric blends of olefin rubber and polyolefin resin |
| US4202801A (en) * | 1977-12-30 | 1980-05-13 | Uniroyal, Inc. | Thermoplastic elastomer composition |
| US4220579A (en) * | 1978-04-17 | 1980-09-02 | Uniroyal, Inc. | Thermoplastic elastomeric blend of monoolefin copolymer rubber, amorphous polypropylene resin and crystalline polyolefin resin |
| US4258145A (en) * | 1979-09-14 | 1981-03-24 | Phillips Petroleum Company | Ternary polymer blends |
| US4386187A (en) * | 1980-06-11 | 1983-05-31 | Sweetheart Plastics, Inc. | Thermoformable polymer blend composition comprising styrene polymer, olefin polymer and block copolymer |
| US4594390A (en) * | 1982-08-23 | 1986-06-10 | Monsanto Company | Process for the preparation of thermoplastic elastomers |
| US4480074A (en) * | 1982-10-20 | 1984-10-30 | Monsanto Company | Process for preparing elastoplastic compositions |
| US4690976A (en) * | 1983-08-01 | 1987-09-01 | The Dow Chemical Company | Blends of olefinic and monovinylidene aromatic polymers |
| US4530795A (en) * | 1984-02-27 | 1985-07-23 | The Upjohn Company | Process for preparation of 16 α-methyl corticoids from Δ16 -steroids |
| US4607074A (en) * | 1984-07-11 | 1986-08-19 | Exxon Research & Engineering Co. | Dynamically cured thermoplastic olefin polymers |
| DE3532357A1 (de) * | 1985-09-11 | 1987-03-19 | Bayer Ag | Thermoplastische elastomere |
| US5011719A (en) * | 1985-11-29 | 1991-04-30 | American National Can Company | Polymeric compositions and films |
| US4843129A (en) * | 1985-12-27 | 1989-06-27 | Exxon Research & Engineering Company | Elastomer-plastic blends |
| US4704431A (en) * | 1986-04-04 | 1987-11-03 | The Dow Chemical Company | Blends of polypropylene and vinylaromatic/α-methylstyrene copolymers |
| US4716197A (en) * | 1986-04-21 | 1987-12-29 | The Dow Chemical Company | Polyethylene/EPDM-graft polystyrene blends |
| US4808665A (en) * | 1987-10-13 | 1989-02-28 | Monsanto Company | Crosslinked blends |
-
1987
- 1987-12-11 IT IT22946/87A patent/IT1223262B/it active
-
1988
- 1988-12-07 AU AU26636/88A patent/AU615697B2/en not_active Ceased
- 1988-12-07 PT PT89189A patent/PT89189B/pt not_active IP Right Cessation
- 1988-12-08 ZA ZA889209A patent/ZA889209B/xx unknown
- 1988-12-08 MX MX1408488A patent/MX14084A/es unknown
- 1988-12-09 DD DD88322933A patent/DD283636A5/de not_active IP Right Cessation
- 1988-12-09 ES ES88120630T patent/ES2055731T5/es not_active Expired - Lifetime
- 1988-12-09 DE DE3850365T patent/DE3850365T3/de not_active Expired - Fee Related
- 1988-12-09 RU SU884613107A patent/RU2074868C1/ru active
- 1988-12-09 BR BR888806525A patent/BR8806525A/pt not_active IP Right Cessation
- 1988-12-09 EP EP88120630A patent/EP0320001B2/en not_active Expired - Lifetime
- 1988-12-09 DK DK686588A patent/DK686588A/da not_active Application Discontinuation
- 1988-12-09 CA CA000585468A patent/CA1334549C/en not_active Expired - Fee Related
- 1988-12-09 CZ CS888145A patent/CZ277978B6/cs unknown
- 1988-12-09 AT AT88120630T patent/ATE107680T1/de active
- 1988-12-09 US US07/282,701 patent/US4889888A/en not_active Expired - Lifetime
- 1988-12-09 NO NO88885477A patent/NO885477L/no unknown
- 1988-12-10 CN CN88109256A patent/CN1035950C/zh not_active Expired - Fee Related
- 1988-12-10 KR KR1019880016440A patent/KR0139092B1/ko not_active IP Right Cessation
- 1988-12-12 JP JP63313650A patent/JP2716487B2/ja not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| CA1334549C (en) | 1995-02-21 |
| NO885477D0 (no) | 1988-12-09 |
| ES2055731T3 (es) | 1994-09-01 |
| IT1223262B (it) | 1990-09-19 |
| JPH01279937A (ja) | 1989-11-10 |
| DK686588D0 (da) | 1988-12-09 |
| JP2716487B2 (ja) | 1998-02-18 |
| EP0320001A2 (en) | 1989-06-14 |
| US4889888A (en) | 1989-12-26 |
| ZA889209B (en) | 1989-08-30 |
| KR0139092B1 (ko) | 1998-05-01 |
| DE3850365T3 (de) | 1999-02-11 |
| DE3850365D1 (de) | 1994-07-28 |
| CZ277978B6 (en) | 1993-07-14 |
| ATE107680T1 (de) | 1994-07-15 |
| ES2055731T5 (es) | 1998-09-16 |
| RU2074868C1 (ru) | 1997-03-10 |
| NO885477L (no) | 1989-06-12 |
| MX14084A (es) | 1994-02-28 |
| PT89189B (pt) | 1993-06-30 |
| PT89189A (pt) | 1989-12-29 |
| CN1034559A (zh) | 1989-08-09 |
| BR8806525A (pt) | 1989-08-22 |
| AU615697B2 (en) | 1991-10-10 |
| CZ814588A3 (en) | 1993-01-13 |
| AU2663688A (en) | 1989-06-15 |
| IT8722946A0 (it) | 1987-12-11 |
| KR890010079A (ko) | 1989-08-05 |
| CN1035950C (zh) | 1997-09-24 |
| DK686588A (da) | 1989-06-12 |
| DE3850365T2 (de) | 1994-10-27 |
| EP0320001B1 (en) | 1994-06-22 |
| EP0320001A3 (en) | 1990-07-18 |
| EP0320001B2 (en) | 1998-06-10 |
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