NL8201893A - Werkwijze voor het bereiden van een thermoplastische vormmassa met een lage oppervlakteglans. - Google Patents

Werkwijze voor het bereiden van een thermoplastische vormmassa met een lage oppervlakteglans. Download PDF

Info

Publication number: NL8201893A
Authority: NL; Netherlands
Prior art keywords: rubber; copolymer; latex; compound; graft copolymer
Prior art date: 1982-05-07

Application number

NL8201893A

Other languages

English (en)

Dutch (nl)

Original Assignee

Stamicarbon

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.)

1982-05-07

Filing date

1982-05-07

Publication date

1983-12-01

Family has litigation

First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=19839704&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=NL8201893(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.

1982-05-07 Application filed by Stamicarbon filed Critical Stamicarbon

1982-05-07 Priority to NL8201893A priority Critical patent/NL8201893A/nl

1983-05-06 Priority to EP83200645A priority patent/EP0094135B1/de

1983-05-06 Priority to DE8383200645T priority patent/DE3363021D1/de

1983-05-06 Priority to AT83200645T priority patent/ATE19259T1/de

1983-12-01 Publication of NL8201893A publication Critical patent/NL8201893A/nl

Links

238000004519 manufacturing process Methods 0.000 title claims description 3
229920001169 thermoplastic Polymers 0.000 title 1
239000004416 thermosoftening plastic Substances 0.000 title 1
229920000126 latex Polymers 0.000 claims abstract description 40
229920001971 elastomer Polymers 0.000 claims abstract description 36
239000005060 rubber Substances 0.000 claims abstract description 36
229920000578 graft copolymer Polymers 0.000 claims abstract description 32
239000004816 latex Substances 0.000 claims abstract description 31
-1 vinyl aromatic compound Chemical class 0.000 claims abstract description 31
229920001577 copolymer Polymers 0.000 claims abstract description 26
239000000203 mixture Substances 0.000 claims abstract description 19
238000000034 method Methods 0.000 claims abstract description 18
229920002554 vinyl polymer Polymers 0.000 claims abstract description 13
150000001875 compounds Chemical class 0.000 claims description 19
229920002857 polybutadiene Polymers 0.000 claims description 9
239000005062 Polybutadiene Substances 0.000 claims description 8
238000000465 moulding Methods 0.000 claims description 7
238000009757 thermoplastic moulding Methods 0.000 claims description 5
229920003048 styrene butadiene rubber Polymers 0.000 claims description 3
238000002360 preparation method Methods 0.000 abstract description 7
239000004415 thermoplastic moulding composition Substances 0.000 abstract 1
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Natural products C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 13
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 7
229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 7
239000003995 emulsifying agent Substances 0.000 description 7
238000007720 emulsion polymerization reaction Methods 0.000 description 7
239000000178 monomer Substances 0.000 description 7
238000006116 polymerization reaction Methods 0.000 description 7
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 6
239000000843 powder Substances 0.000 description 5
229920000638 styrene acrylonitrile Polymers 0.000 description 5
KAKZBPTYRLMSJV-UHFFFAOYSA-N vinyl-ethylene Natural products C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 5
IYAVYMAGJPJCNJ-UHFFFAOYSA-N S=[SH2] Chemical compound S=[SH2] IYAVYMAGJPJCNJ-UHFFFAOYSA-N 0.000 description 4
239000003999 initiator Substances 0.000 description 4
150000002898 organic sulfur compounds Chemical class 0.000 description 4
229920002959 polymer blend Polymers 0.000 description 4
239000000047 product Substances 0.000 description 4
239000007787 solid Substances 0.000 description 4
230000003068 static effect Effects 0.000 description 4
FHVDTGUDJYJELY-UHFFFAOYSA-N 6-{[2-carboxy-4,5-dihydroxy-6-(phosphanyloxy)oxan-3-yl]oxy}-4,5-dihydroxy-3-phosphanyloxane-2-carboxylic acid Chemical compound O1C(C(O)=O)C(P)C(O)C(O)C1OC1C(C(O)=O)OC(OP)C(O)C1O FHVDTGUDJYJELY-UHFFFAOYSA-N 0.000 description 3
RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 3
239000002253 acid Substances 0.000 description 3
229940072056 alginate Drugs 0.000 description 3
235000010443 alginic acid Nutrition 0.000 description 3
229920000615 alginic acid Polymers 0.000 description 3
XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 3
239000002245 particle Substances 0.000 description 3
IANQTJSKSUMEQM-UHFFFAOYSA-N 1-benzofuran Chemical compound C1=CC=C2OC=CC2=C1 IANQTJSKSUMEQM-UHFFFAOYSA-N 0.000 description 2
YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Chemical compound C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 description 2
XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
125000000217 alkyl group Chemical group 0.000 description 2
239000003963 antioxidant agent Substances 0.000 description 2
235000006708 antioxidants Nutrition 0.000 description 2
238000005452 bending Methods 0.000 description 2
239000007795 chemical reaction product Substances 0.000 description 2
230000015271 coagulation Effects 0.000 description 2
238000005345 coagulation Methods 0.000 description 2
238000005520 cutting process Methods 0.000 description 2
239000012467 final product Substances 0.000 description 2
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 2
229910052751 metal Inorganic materials 0.000 description 2
239000002184 metal Substances 0.000 description 2
KZCOBXFFBQJQHH-UHFFFAOYSA-N octane-1-thiol Chemical compound CCCCCCCCS KZCOBXFFBQJQHH-UHFFFAOYSA-N 0.000 description 2
229920002285 poly(styrene-co-acrylonitrile) Polymers 0.000 description 2
150000003839 salts Chemical class 0.000 description 2
239000000344 soap Substances 0.000 description 2
239000000126 substance Substances 0.000 description 2
PRBHEGAFLDMLAL-GQCTYLIASA-N (4e)-hexa-1,4-diene Chemical compound C\C=C\CC=C PRBHEGAFLDMLAL-GQCTYLIASA-N 0.000 description 1
UUUYXCLERBDLEO-UHFFFAOYSA-N 1-hydroperoxy-1-methylcyclohexane Chemical compound OOC1(C)CCCCC1 UUUYXCLERBDLEO-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
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
ZJCZFAAXZODMQT-UHFFFAOYSA-N 2-methylpentadecane-2-thiol Chemical group CCCCCCCCCCCCCC(C)(C)S ZJCZFAAXZODMQT-UHFFFAOYSA-N 0.000 description 1
FRQQKWGDKVGLFI-UHFFFAOYSA-N 2-methylundecane-2-thiol Chemical compound CCCCCCCCCC(C)(C)S FRQQKWGDKVGLFI-UHFFFAOYSA-N 0.000 description 1
FRIBMENBGGCKPD-UHFFFAOYSA-N 3-(2,3-dimethoxyphenyl)prop-2-enal Chemical compound COC1=CC=CC(C=CC=O)=C1OC FRIBMENBGGCKPD-UHFFFAOYSA-N 0.000 description 1
OCVLSHAVSIYKLI-UHFFFAOYSA-N 3h-1,3-thiazole-2-thione Chemical class SC1=NC=CS1 OCVLSHAVSIYKLI-UHFFFAOYSA-N 0.000 description 1
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
239000004709 Chlorinated polyethylene Substances 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
229920002943 EPDM rubber Polymers 0.000 description 1
JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 description 1
229920000459 Nitrile rubber Polymers 0.000 description 1
239000002174 Styrene-butadiene Substances 0.000 description 1
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
150000001252 acrylic acid derivatives Chemical class 0.000 description 1
239000000654 additive Substances 0.000 description 1
239000003513 alkali Substances 0.000 description 1
150000001336 alkenes Chemical class 0.000 description 1
150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
125000005907 alkyl ester group Chemical group 0.000 description 1
ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium peroxydisulfate Substances [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 1
VAZSKTXWXKYQJF-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)OOS([O-])=O VAZSKTXWXKYQJF-UHFFFAOYSA-N 0.000 description 1
229910001870 ammonium persulfate Inorganic materials 0.000 description 1
230000003078 antioxidant effect Effects 0.000 description 1
125000001204 arachidyl 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])C([H])([H])C([H])([H])[H] 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
125000005228 aryl sulfonate group Chemical group 0.000 description 1
125000000751 azo group Chemical group [*]N=N[*] 0.000 description 1
WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
229910052794 bromium Inorganic materials 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
125000004432 carbon atom Chemical group C* 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
239000003638 chemical reducing agent Substances 0.000 description 1
229920006235 chlorinated polyethylene elastomer Polymers 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
239000000460 chlorine Substances 0.000 description 1
238000007334 copolymerization reaction Methods 0.000 description 1
238000004132 cross linking Methods 0.000 description 1
SPTHWAJJMLCAQF-UHFFFAOYSA-M ctk4f8481 Chemical compound [O-]O.CC(C)C1=CC=CC=C1C(C)C SPTHWAJJMLCAQF-UHFFFAOYSA-M 0.000 description 1
LTUFFQPUELZQBJ-UHFFFAOYSA-N cyclododeca-1,3-diene-1-thiol Chemical group SC1=CC=CCCCCCCCC1 LTUFFQPUELZQBJ-UHFFFAOYSA-N 0.000 description 1
239000008121 dextrose Substances 0.000 description 1
150000001993 dienes Chemical class 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
239000000539 dimer Substances 0.000 description 1
150000002019 disulfides Chemical class 0.000 description 1
WNAHIZMDSQCWRP-UHFFFAOYSA-N dodecane-1-thiol Chemical compound CCCCCCCCCCCCS WNAHIZMDSQCWRP-UHFFFAOYSA-N 0.000 description 1
125000003438 dodecyl group Chemical group [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])* 0.000 description 1
238000001035 drying Methods 0.000 description 1
125000000219 ethylidene group Chemical group [H]C(=[*])C([H])([H])[H] 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
150000004665 fatty acids Chemical class 0.000 description 1
235000003891 ferrous sulphate Nutrition 0.000 description 1
239000011790 ferrous sulphate Substances 0.000 description 1
ISXSFOPKZQZDAO-UHFFFAOYSA-N formaldehyde;sodium Chemical compound [Na].O=C ISXSFOPKZQZDAO-UHFFFAOYSA-N 0.000 description 1
229910052736 halogen Inorganic materials 0.000 description 1
150000002367 halogens Chemical class 0.000 description 1
229920001519 homopolymer Polymers 0.000 description 1
150000002432 hydroperoxides Chemical class 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 description 1
229910000359 iron(II) sulfate Inorganic materials 0.000 description 1
239000000314 lubricant Substances 0.000 description 1
239000000463 material Substances 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
SEXOVMIIVBKGGM-UHFFFAOYSA-N naphthalene-1-thiol Chemical compound C1=CC=C2C(S)=CC=CC2=C1 SEXOVMIIVBKGGM-UHFFFAOYSA-N 0.000 description 1
ZVEZMVFBMOOHAT-UHFFFAOYSA-N nonane-1-thiol Chemical group CCCCCCCCCS ZVEZMVFBMOOHAT-UHFFFAOYSA-N 0.000 description 1
JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical class OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 1
150000002978 peroxides Chemical class 0.000 description 1
JRKICGRDRMAZLK-UHFFFAOYSA-L persulfate group Chemical group S(=O)(=O)([O-])OOS(=O)(=O)[O-] JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
239000000049 pigment Substances 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
239000004033 plastic Substances 0.000 description 1
229920001084 poly(chloroprene) Polymers 0.000 description 1
229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
229920000570 polyether Polymers 0.000 description 1
229920005862 polyol Polymers 0.000 description 1
150000003077 polyols Chemical class 0.000 description 1
XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 1
239000012966 redox initiator Substances 0.000 description 1
229920005989 resin Polymers 0.000 description 1
239000011347 resin Substances 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
239000002002 slurry Substances 0.000 description 1
FQENQNTWSFEDLI-UHFFFAOYSA-J sodium diphosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])([O-])=O FQENQNTWSFEDLI-UHFFFAOYSA-J 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
229940048086 sodium pyrophosphate Drugs 0.000 description 1
125000003011 styrenyl group Chemical group [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
239000011593 sulfur Substances 0.000 description 1
229910052717 sulfur Inorganic materials 0.000 description 1
150000003508 terpinolene derivatives Chemical class 0.000 description 1
CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 1
235000019818 tetrasodium diphosphate Nutrition 0.000 description 1
239000001577 tetrasodium phosphonato phosphate Substances 0.000 description 1
KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 1
229960002447 thiram Drugs 0.000 description 1
IPBROXKVGHZHJV-UHFFFAOYSA-N tridecane-1-thiol Chemical group CCCCCCCCCCCCCS IPBROXKVGHZHJV-UHFFFAOYSA-N 0.000 description 1
238000007666 vacuum forming Methods 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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
- 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
- C08L25/08—Copolymers of styrene
- C08L25/12—Copolymers of styrene with unsaturated nitriles
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L21/00—Compositions of unspecified rubbers
- 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
- C08L51/04—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 rubbers
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L55/00—Compositions of homopolymers or copolymers, obtained by polymerisation reactions only involving carbon-to-carbon unsaturated bonds, not provided for in groups C08L23/00 - C08L53/00
- C08L55/02—ABS [Acrylonitrile-Butadiene-Styrene] polymers
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L9/00—Compositions of homopolymers or copolymers of conjugated diene hydrocarbons

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)

NL8201893A 1982-05-07 1982-05-07 Werkwijze voor het bereiden van een thermoplastische vormmassa met een lage oppervlakteglans. NL8201893A (nl)

Priority Applications (4)

Application Number	Priority Date	Filing Date	Title
NL8201893A NL8201893A (nl)	1982-05-07	1982-05-07	Werkwijze voor het bereiden van een thermoplastische vormmassa met een lage oppervlakteglans.
EP83200645A EP0094135B1 (de)	1982-05-07	1983-05-06	Verfahren zur Herstellung einer thermoplastischen Formmassazusammensetzung mit niedrigem Oberflächenglanz
DE8383200645T DE3363021D1 (en)	1982-05-07	1983-05-06	Process for the preparation of a thermoplastic moulding composition with low surface gloss
AT83200645T ATE19259T1 (de)	1982-05-07	1983-05-06	Verfahren zur herstellung einer thermoplastischen formmassazusammensetzung mit niedrigem oberflaechenglanz.

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
NL8201893A NL8201893A (nl)	1982-05-07	1982-05-07	Werkwijze voor het bereiden van een thermoplastische vormmassa met een lage oppervlakteglans.
NL8201893		1982-05-07

Publications (1)

Publication Number	Publication Date
NL8201893A true NL8201893A (nl)	1983-12-01

Family

ID=19839704

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NL8201893A NL8201893A (nl)	1982-05-07	1982-05-07	Werkwijze voor het bereiden van een thermoplastische vormmassa met een lage oppervlakteglans.

Country Status (4)

Country	Link
EP (1)	EP0094135B1 (de)
AT (1)	ATE19259T1 (de)
DE (1)	DE3363021D1 (de)
NL (1)	NL8201893A (de)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3805057A1 (de) *	1988-02-18	1989-08-31	Bayer Ag	Hochzaehe abs-formmassen mit matter oberflaeche
US5081193A (en) *	1989-01-23	1992-01-14	Hitachi Chemical Company Ltd.	Low gloss agents, process for production thereof, low gloss thermoplastic resin compositions, and molded articles
EP3298079B1 (de)	2015-05-18	2019-01-23	INEOS Styrolution Group GmbH	Abs-formmasse mit guter eigenschaftskombination von verarbeitbarkeit und oberflächenqualität

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
BE637324A (de) *	1962-09-14
GB1125382A (en) *	1964-09-11	1968-08-28	Goodyear Tire & Rubber	Clear impact resistant resin
US3773552A (en) *	1971-11-17	1973-11-20	Dow Chemical Co	Process of providing uniform gloss,lacquer coated alkenyl aromatic resin article
US4374952A (en) *	1980-07-14	1983-02-22	Uniroyal, Inc.	Nitrile rubber/EPDM graft blends

1982
- 1982-05-07 NL NL8201893A patent/NL8201893A/nl not_active Application Discontinuation
1983
- 1983-05-06 DE DE8383200645T patent/DE3363021D1/de not_active Expired
- 1983-05-06 EP EP83200645A patent/EP0094135B1/de not_active Expired
- 1983-05-06 AT AT83200645T patent/ATE19259T1/de not_active IP Right Cessation

Also Published As

Publication number	Publication date
EP0094135B1 (de)	1986-04-16
DE3363021D1 (en)	1986-05-22
ATE19259T1 (de)	1986-05-15
EP0094135A1 (de)	1983-11-16

Legal Events

Date	Code	Title	Description
1983-12-01	A1B	A search report has been drawn up
1985-01-02	BV	The patent application has lapsed

Publication	Publication Date	Title
FI74718C (fi)	1988-03-10	Polymerkompositon baserad pao ett polykarbonat, en kopolymer och en ympsampolymer.
EP0013052B1 (de)	1983-06-01	Copolymer von Kern-Bromiertem Styrol und Acrylnitril und Verfahren zur Herstellung eines derartigen Copolymers
EP0043613B1 (de)	1984-05-16	Polymerzusammensetzung und daraus hergestellter Gegenstand
EP0051336A1 (de)	1982-05-12	Polymerzusammensetzung
NL8201893A (nl)	1983-12-01	Werkwijze voor het bereiden van een thermoplastische vormmassa met een lage oppervlakteglans.
EP0048059B1 (de)	1986-01-02	Polymerzusammensetzung von Pfropfcopolymeren aus Styrol und Acrylnitril gepfropft auf Kautschuk
NL8300064A (nl)	1984-08-01	Gestabiliseerde polymeercompositie.
US5804656A (en)	1998-09-08	Compositions of the ABS type for processing by extrusion and deep drawing
NL8105135A (nl)	1983-06-01	Polymeercompositie.
EP0307537B1 (de)	1992-05-20	Schwefelhaltige Polymerisate
NL8003798A (nl)	1982-02-01	Copolymeer van alfa-methylstyreen en acrylonitril.
JPH072822B2 (ja)	1995-01-18	高モノマー転化率を有する熱可塑性樹脂の製造方法
KR100774820B1 (ko)	2007-11-07	흐름성과 무도장 특성이 우수한 열가소성 수지 조성물
EP0046320B1 (de)	1984-11-28	Verfahren zur Herstellung eines Copolymers
JP3827462B2 (ja)	2006-09-27	高ニトリル系重合体組成物及びその製造方法
FI73706B (fi)	1987-07-31	Polymerkomposition baserad pao styrenderivat, akrylnitril och gummi.
DE3505778A1 (de)	1986-08-21	Schwefelhaltige pfropfprodukte
JPS6246564B2 (de)	1987-10-02
NL8102415A (nl)	1982-12-16	Werkwijze voor het bereiden van een copolymeer.
JPS614713A (ja)	1986-01-10	熱可塑性樹脂の製造方法
JP2002226653A (ja)	2002-08-14	ゴム変性熱可塑性重合体組成物
NL7907369A (nl)	1981-04-07	Styreenpolymeercompositie.
NL8501253A (nl)	1986-12-01	Polymeercompositie.