LU85713A1 - Procede de preparation de polystyrene-choc presentant un bon comportement aux agents corrosifs - Google Patents
Procede de preparation de polystyrene-choc presentant un bon comportement aux agents corrosifs Download PDFInfo
- Publication number
- LU85713A1 LU85713A1 LU85713A LU85713A LU85713A1 LU 85713 A1 LU85713 A1 LU 85713A1 LU 85713 A LU85713 A LU 85713A LU 85713 A LU85713 A LU 85713A LU 85713 A1 LU85713 A1 LU 85713A1
- Authority
- LU
- Luxembourg
- Prior art keywords
- weight
- rubber
- parts
- styrene
- solution
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 23
- 238000002360 preparation method Methods 0.000 title claims description 4
- 239000003518 caustics Substances 0.000 title description 5
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 51
- 229920000642 polymer Polymers 0.000 claims description 31
- 229920001971 elastomer Polymers 0.000 claims description 26
- 239000005060 rubber Substances 0.000 claims description 24
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 claims description 22
- 239000000654 additive Substances 0.000 claims description 16
- 239000000203 mixture Substances 0.000 claims description 14
- -1 polyethylene Polymers 0.000 claims description 14
- 229920002857 polybutadiene Polymers 0.000 claims description 13
- 239000001993 wax Substances 0.000 claims description 13
- 125000000129 anionic group Chemical group 0.000 claims description 12
- 239000000539 dimer Substances 0.000 claims description 11
- 238000006116 polymerization reaction Methods 0.000 claims description 10
- 239000004698 Polyethylene Substances 0.000 claims description 8
- 150000001875 compounds Chemical class 0.000 claims description 8
- 229920000573 polyethylene Polymers 0.000 claims description 8
- 239000005062 Polybutadiene Substances 0.000 claims description 7
- 238000005336 cracking Methods 0.000 claims description 7
- 229920002545 silicone oil Polymers 0.000 claims description 6
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 6
- 239000004615 ingredient Substances 0.000 claims description 5
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 claims description 4
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 claims description 4
- RMPAXPOFLJVREM-UHFFFAOYSA-N (1-phenylcyclobutyl)benzene Chemical compound C1CCC1(C=1C=CC=CC=1)C1=CC=CC=C1 RMPAXPOFLJVREM-UHFFFAOYSA-N 0.000 claims description 3
- YASDJUXENMYIBH-UHFFFAOYSA-N 3-methyl-3-phenyl-1,2-dihydroindene Chemical compound C1CC2=CC=CC=C2C1(C)C1=CC=CC=C1 YASDJUXENMYIBH-UHFFFAOYSA-N 0.000 claims description 3
- 239000002202 Polyethylene glycol Substances 0.000 claims description 3
- 230000000996 additive effect Effects 0.000 claims description 3
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical class [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 claims description 3
- WNAHIZMDSQCWRP-UHFFFAOYSA-N dodecane-1-thiol Chemical compound CCCCCCCCCCCCS WNAHIZMDSQCWRP-UHFFFAOYSA-N 0.000 claims description 3
- 229920001223 polyethylene glycol Polymers 0.000 claims description 3
- SWMVJOXVIGSMEN-UHFFFAOYSA-N 3-phenylbuta-1,3-dienylbenzene Chemical compound C=1C=CC=CC=1C(=C)C=CC1=CC=CC=C1 SWMVJOXVIGSMEN-UHFFFAOYSA-N 0.000 claims description 2
- 239000000470 constituent Substances 0.000 claims description 2
- 230000001747 exhibiting effect Effects 0.000 claims description 2
- 125000003827 glycol group Chemical group 0.000 claims description 2
- 239000005662 Paraffin oil Substances 0.000 description 10
- 239000000499 gel Substances 0.000 description 10
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- 238000012360 testing method Methods 0.000 description 8
- 238000004519 manufacturing process Methods 0.000 description 7
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 239000004793 Polystyrene Substances 0.000 description 5
- 239000003963 antioxidant agent Substances 0.000 description 5
- 229920002223 polystyrene Polymers 0.000 description 5
- 230000008961 swelling Effects 0.000 description 5
- 239000003153 chemical reaction reagent Substances 0.000 description 4
- 230000007797 corrosion Effects 0.000 description 4
- 238000005260 corrosion Methods 0.000 description 4
- 230000009477 glass transition Effects 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- 235000019198 oils Nutrition 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- 150000002978 peroxides Chemical class 0.000 description 4
- 230000003078 antioxidant effect Effects 0.000 description 3
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- YGVYHUGLHHFGNN-UHFFFAOYSA-N (2-phenylcyclobuten-1-yl)benzene Chemical compound C1CC(C=2C=CC=CC=2)=C1C1=CC=CC=C1 YGVYHUGLHHFGNN-UHFFFAOYSA-N 0.000 description 2
- 239000004604 Blowing Agent Substances 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 2
- 238000012662 bulk polymerization Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 239000000806 elastomer Substances 0.000 description 2
- 239000011159 matrix material Substances 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 238000000691 measurement method Methods 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 239000012778 molding material Substances 0.000 description 2
- 239000012188 paraffin wax Substances 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- IEMCJUJOHAEFFW-UHFFFAOYSA-M potassium 2-[(2-acetyloxybenzoyl)amino]ethanesulfonate Chemical compound CC(=O)OC1=CC=CC=C1C(=O)NCCS(=O)(=O)[O-].[K+] IEMCJUJOHAEFFW-UHFFFAOYSA-M 0.000 description 2
- YAPRWCFMWHUXRS-UHFFFAOYSA-N (2-hydroxyphenyl) propanoate Chemical compound CCC(=O)OC1=CC=CC=C1O YAPRWCFMWHUXRS-UHFFFAOYSA-N 0.000 description 1
- PAOHAQSLJSMLAT-UHFFFAOYSA-N 1-butylperoxybutane Chemical group CCCCOOCCCC PAOHAQSLJSMLAT-UHFFFAOYSA-N 0.000 description 1
- NVZWEEGUWXZOKI-UHFFFAOYSA-N 1-ethenyl-2-methylbenzene Chemical compound CC1=CC=CC=C1C=C NVZWEEGUWXZOKI-UHFFFAOYSA-N 0.000 description 1
- BTOVVHWKPVSLBI-UHFFFAOYSA-N 2-methylprop-1-enylbenzene Chemical class CC(C)=CC1=CC=CC=C1 BTOVVHWKPVSLBI-UHFFFAOYSA-N 0.000 description 1
- MPKIZIGHGVKHDY-UHFFFAOYSA-N 2-tert-butyl-5-methylbenzene-1,4-diol Chemical compound CC1=CC(O)=C(C(C)(C)C)C=C1O MPKIZIGHGVKHDY-UHFFFAOYSA-N 0.000 description 1
- LGLDSEPDYUTBNZ-UHFFFAOYSA-N 3-phenylbuta-1,3-dien-2-ylbenzene Chemical compound C=1C=CC=CC=1C(=C)C(=C)C1=CC=CC=C1 LGLDSEPDYUTBNZ-UHFFFAOYSA-N 0.000 description 1
- JLBJTVDPSNHSKJ-UHFFFAOYSA-N 4-Methylstyrene Chemical compound CC1=CC=C(C=C)C=C1 JLBJTVDPSNHSKJ-UHFFFAOYSA-N 0.000 description 1
- 125000004203 4-hydroxyphenyl group Chemical group [H]OC1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 102100023779 40S ribosomal protein S5 Human genes 0.000 description 1
- 241000251468 Actinopterygii Species 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 1
- 239000005745 Captan Substances 0.000 description 1
- 101000622644 Homo sapiens 40S ribosomal protein S5 Proteins 0.000 description 1
- 240000007930 Oxalis acetosella Species 0.000 description 1
- 235000008098 Oxalis acetosella Nutrition 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 239000008186 active pharmaceutical agent Substances 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- NTXGQCSETZTARF-UHFFFAOYSA-N buta-1,3-diene;prop-2-enenitrile Chemical compound C=CC=C.C=CC#N NTXGQCSETZTARF-UHFFFAOYSA-N 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- 229940117949 captan Drugs 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000013043 chemical agent Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000013065 commercial product Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 229910003460 diamond Inorganic materials 0.000 description 1
- 239000010432 diamond Substances 0.000 description 1
- 238000001493 electron microscopy Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 125000005456 glyceride group Chemical group 0.000 description 1
- UHUSDOQQWJGJQS-UHFFFAOYSA-N glycerol 1,2-dioctadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(CO)OC(=O)CCCCCCCCCCCCCCCCC UHUSDOQQWJGJQS-UHFFFAOYSA-N 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 229940057995 liquid paraffin Drugs 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- SSDSCDGVMJFTEQ-UHFFFAOYSA-N octadecyl 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 SSDSCDGVMJFTEQ-UHFFFAOYSA-N 0.000 description 1
- 235000014593 oils and fats Nutrition 0.000 description 1
- 239000004006 olive oil Substances 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 239000002530 phenolic antioxidant Substances 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- QROGIFZRVHSFLM-UHFFFAOYSA-N prop-1-enylbenzene Chemical class CC=CC1=CC=CC=C1 QROGIFZRVHSFLM-UHFFFAOYSA-N 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 150000003440 styrenes Chemical class 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229920001897 terpolymer Polymers 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000011240 wet gel Substances 0.000 description 1
Classifications
-
- 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
- C08F279/00—Macromolecular compounds obtained by polymerising monomers on to polymers of monomers having two or more carbon-to-carbon double bonds as defined in group C08F36/00
- C08F279/02—Macromolecular compounds obtained by polymerising monomers on to polymers of monomers having two or more carbon-to-carbon double bonds as defined in group C08F36/00 on to polymers of conjugated dienes
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Graft Or Block Polymers (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Polymerisation Methods In General (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR8321059 | 1983-12-30 | ||
| FR8321059A FR2557575B1 (fr) | 1983-12-30 | 1983-12-30 | Procede de preparation de polystyrene-choc presentant un bon comportement aux agents corrosifs |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| LU85713A1 true LU85713A1 (fr) | 1985-07-24 |
Family
ID=9295733
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| LU85713A LU85713A1 (fr) | 1983-12-30 | 1984-12-27 | Procede de preparation de polystyrene-choc presentant un bon comportement aux agents corrosifs |
Country Status (15)
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3686681B2 (ja) * | 1992-03-10 | 2005-08-24 | 住友化学株式会社 | ゴム変性スチレン系樹脂組成物 |
| DE69624062T3 (de) | 1995-10-25 | 2006-09-21 | Fina Technology, Inc., Houston | Monovinylaromatische Polymere mit verbesserter Spannungsrissbeständigkeit |
| RU2294941C2 (ru) * | 2005-04-06 | 2007-03-10 | Открытое акционерное общество "Пластполимер" | Способ получения стойкого к растрескиванию ударопрочного полистирола |
| US7638559B2 (en) | 2005-05-10 | 2009-12-29 | Nova Chemicals Inc. | Expandable resins |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2646418A (en) * | 1951-05-25 | 1953-07-21 | Dow Chemical Co | Process for polymerizing monovinyl aromatic compounds with rubber |
| IT647966A (enrdf_load_stackoverflow) * | 1960-01-25 | 1900-01-01 | ||
| DE1495638B2 (de) * | 1960-09-07 | 1973-03-22 | Farbwerke Hoechst AG, vormals Meister Lucius & Brüning, 6000 Frankfurt | Verfahren zur herstellung von schlagfestem polystyrol |
| NL279121A (enrdf_load_stackoverflow) * | 1961-06-01 | |||
| GB1025573A (en) * | 1962-12-24 | 1966-04-14 | Foster Grant Co Inc | Improvements in or relating to polymer processes and compositions |
| FR1351613A (fr) * | 1963-01-07 | 1964-02-07 | Dow Chemical Co | Compositions polymérisées oléfiniques à base de résines et d'élastomères et leur procédé d'obtention |
| CA936297A (en) * | 1963-08-15 | 1973-10-30 | Dart Industries Inc. | Impact resistant graft copolymers |
| DE1495837C3 (de) * | 1964-09-30 | 1974-02-14 | Bayer Ag, 5090 Leverkusen | Verfahren zur Herstellung thermoplastisch-elastischer Formmassen |
| GB1229409A (enrdf_load_stackoverflow) * | 1967-05-11 | 1971-04-21 | ||
| JPS5917126B2 (ja) * | 1979-03-29 | 1984-04-19 | 旭化成株式会社 | 改良された耐衝撃性スチレン系重合体の製法 |
| JPS5919577B2 (ja) * | 1980-08-25 | 1984-05-07 | 日本エラストマ−株式会社 | 耐衝撃性ポリスチレンの製造方法 |
| DE3047303A1 (de) * | 1980-12-16 | 1982-07-29 | Basf Ag, 6700 Ludwigshafen | Verfahren zur kontinuierlichen herstellung von mit kautschuk modifizierten polymerisaten von vinylaromaten, verwendung derselben zum spritzgiessen, sowie formteile aus diesen |
| FR2505342A1 (fr) * | 1981-05-07 | 1982-11-12 | Bp Chemical Ltd | Procede de fabrication d'un polymere vinyl-aromatique tres tenace |
-
1983
- 1983-12-30 FR FR8321059A patent/FR2557575B1/fr not_active Expired
-
1984
- 1984-12-13 GB GB08431498A patent/GB2153370B/en not_active Expired
- 1984-12-20 DE DE3446592A patent/DE3446592A1/de not_active Ceased
- 1984-12-20 IT IT24147/84A patent/IT1177474B/it active
- 1984-12-21 DK DK626184A patent/DK626184A/da not_active Application Discontinuation
- 1984-12-21 CA CA000470934A patent/CA1241484A/fr not_active Expired
- 1984-12-24 NL NL8403940A patent/NL191336C/xx not_active IP Right Cessation
- 1984-12-27 LU LU85713A patent/LU85713A1/fr unknown
- 1984-12-27 CH CH6193/84A patent/CH662815A5/fr not_active IP Right Cessation
- 1984-12-27 NO NO845237A patent/NO845237L/no unknown
- 1984-12-28 BE BE0/214272A patent/BE901418A/fr not_active IP Right Cessation
- 1984-12-28 SE SE8406665A patent/SE465879B/sv unknown
- 1984-12-28 AT AT0412184A patent/AT394369B/de not_active IP Right Cessation
- 1984-12-29 KR KR1019840008533A patent/KR920006762B1/ko not_active Expired
- 1984-12-29 JP JP59282028A patent/JPS60158212A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| SE465879B (sv) | 1991-11-11 |
| SE8406665L (sv) | 1985-07-01 |
| IT1177474B (it) | 1987-08-26 |
| NL191336C (nl) | 1995-06-01 |
| NO845237L (no) | 1985-07-01 |
| GB2153370B (en) | 1987-12-23 |
| ATA412184A (de) | 1991-09-15 |
| KR850004786A (ko) | 1985-07-27 |
| IT8424147A0 (it) | 1984-12-20 |
| NL191336B (nl) | 1995-01-02 |
| GB2153370A (en) | 1985-08-21 |
| BE901418A (fr) | 1985-06-28 |
| FR2557575A1 (fr) | 1985-07-05 |
| DE3446592A1 (de) | 1985-07-11 |
| KR920006762B1 (ko) | 1992-08-17 |
| DK626184D0 (da) | 1984-12-21 |
| GB8431498D0 (en) | 1985-01-23 |
| CH662815A5 (fr) | 1987-10-30 |
| DK626184A (da) | 1985-07-01 |
| CA1241484A (fr) | 1988-08-30 |
| SE8406665D0 (sv) | 1984-12-28 |
| JPS60158212A (ja) | 1985-08-19 |
| JPS6343413B2 (enrdf_load_stackoverflow) | 1988-08-30 |
| AT394369B (de) | 1992-03-25 |
| FR2557575B1 (fr) | 1987-02-06 |
| NL8403940A (nl) | 1985-07-16 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| RU2138524C1 (ru) | Концентрат, пригодный для получения функционализированных полиолефинов, способ получения концентрата, способы функционализации гомополимеров и сополимеров олефинов, функционализированный полиолефин | |
| WO1993018092A1 (fr) | Procede de preparation de compositions bitume-polymere, application des compositions obtenues a la realisation de revetements et solution mere de polymere pour l'obtention desdites compositions | |
| Filippi et al. | Reactive compatibilizer precursors for LDPE/PA6 blends, 1. Ethylene/acrylic acid copolymers | |
| FR2682961A1 (fr) | Peinture lubrifiante pour plaques d'acier ou d'aluminium. | |
| FR2699187A1 (fr) | Emulsions aqueuses bitume-polymère, leur procédé de préparation et leurs applications. | |
| US3630905A (en) | Oil-extended vi improvers | |
| EP0731816B1 (fr) | Composition comprenant un polymere vinylaromatique et un caoutchouc et son procede d'obtention | |
| LU85713A1 (fr) | Procede de preparation de polystyrene-choc presentant un bon comportement aux agents corrosifs | |
| JPS60133044A (ja) | Ａｂｓ組成物およびその製法 | |
| EP0130855B1 (fr) | Compositions thermoplastiques contenant un polymère greffé par des silanes permettant d'améliorer les propriétés physiques d'une polyoléfine thermoplastique, procédé permettant cette amélioration | |
| EP0044234B1 (fr) | Procédé de préparation de copolymères de greffage par irradiation | |
| CA1211249A (fr) | COMPOSITIONS POLYMERES RETICULEES DE L'ETHYLENE ET D'AU MOINS UNE .alpha.-OLEFINE, UN PROCEDE POUR LEUR PREPARATION ET LEUR APPLICATION A LA FABRICATION DE CABLES POUR LE TRANSPORT DU COURANT ELECTRIQUE | |
| FR2521150A1 (fr) | Procede de preparation de polymeres greffes de styrene | |
| WO2000055211A1 (fr) | Procede de preparation d'un caoutchouc porteur de radical libre stable et utilisation dudit caoutchouc porteur pour la preparation d'un polymere vinylaromatique choc | |
| Hassan et al. | Thermal, physico‐mechanical, and morphological properties of HDPE graft‐copolymerized with polystyrene | |
| FR2460965A1 (fr) | Procede et utilisation dudit procede pour la fabrication de terpolymeres elastomeres d'ethylene, de propylene et de dienes | |
| KR100642426B1 (ko) | 저온 내충격성이 우수한 스티렌계 열가소성 수지 조성물 | |
| FR2631345A1 (fr) | Composition de resine thermoplastique a teneur en halogene | |
| EP0044233B1 (fr) | Procédé de préparation de copolymères greffés à base de styrène et d'un polymère caoutchouteux | |
| FR3077577A1 (fr) | Composition de résine, article moulé, appareil destiné à être en contact avec les aliments et récipient destiné à être en contact avec les aliments | |
| EP0514245A1 (fr) | Compositions à base de polymère de chlorure de vinyle et de polyoléfine à propriétés rhéologiques améliorées leur procédé de synthèse et leur utilisation | |
| FR2559774A1 (fr) | Procede pour ameliorer les proprietes adhesives des polyolefines | |
| NO771149L (no) | Ekstraksjonsresistente stabiliserende midler for polyolefiner | |
| BE471977A (enrdf_load_stackoverflow) | ||
| BE1011929A3 (fr) | Polymere du propylene, procede pour son obtention et utilisation. |