CA2044176A1 - Copolymeres plastifies de triester de composes aromatiques et d'acrylonitrile et de styrene - Google Patents
Copolymeres plastifies de triester de composes aromatiques et d'acrylonitrile et de styreneInfo
- Publication number
- CA2044176A1 CA2044176A1 CA002044176A CA2044176A CA2044176A1 CA 2044176 A1 CA2044176 A1 CA 2044176A1 CA 002044176 A CA002044176 A CA 002044176A CA 2044176 A CA2044176 A CA 2044176A CA 2044176 A1 CA2044176 A1 CA 2044176A1
- Authority
- CA
- Canada
- Prior art keywords
- styrene
- acrylonitrile
- triester
- aromatic
- copolymers
- Prior art date
- Legal status (The legal status 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 status listed.)
- Abandoned
Links
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 title claims abstract description 24
- 229920001577 copolymer Polymers 0.000 title claims abstract description 21
- -1 Aromatic triester Chemical class 0.000 title claims abstract description 19
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 title claims description 10
- 239000004014 plasticizer Substances 0.000 claims description 18
- 239000000203 mixture Substances 0.000 claims description 13
- ARCGXLSVLAOJQL-UHFFFAOYSA-N anhydrous trimellitic acid Natural products OC(=O)C1=CC=C(C(O)=O)C(C(O)=O)=C1 ARCGXLSVLAOJQL-UHFFFAOYSA-N 0.000 claims description 6
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- JNXDCMUUZNIWPQ-UHFFFAOYSA-N trioctyl benzene-1,2,4-tricarboxylate Chemical group CCCCCCCCOC(=O)C1=CC=C(C(=O)OCCCCCCCC)C(C(=O)OCCCCCCCC)=C1 JNXDCMUUZNIWPQ-UHFFFAOYSA-N 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims 1
- SMYKBXMWXCZOLU-UHFFFAOYSA-N tris-decyl benzene-1,2,4-tricarboxylate Chemical compound CCCCCCCCCCOC(=O)C1=CC=C(C(=O)OCCCCCCCCCC)C(C(=O)OCCCCCCCCCC)=C1 SMYKBXMWXCZOLU-UHFFFAOYSA-N 0.000 claims 1
- 229920000642 polymer Polymers 0.000 description 8
- 235000012424 soybean oil Nutrition 0.000 description 5
- 239000003549 soybean oil Substances 0.000 description 5
- 150000005691 triesters Chemical class 0.000 description 5
- 238000000465 moulding Methods 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 239000000155 melt Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 230000035900 sweating Effects 0.000 description 3
- 125000005591 trimellitate group Chemical group 0.000 description 3
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- 239000004609 Impact Modifier Substances 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 150000005840 aryl radicals Chemical class 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 238000002845 discoloration Methods 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000005060 rubber Substances 0.000 description 2
- 210000004243 sweat Anatomy 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- FEFCILUKYGHITK-UHFFFAOYSA-N 2-decoxycarbonylbenzoic acid Chemical compound CCCCCCCCCCOC(=O)C1=CC=CC=C1C(O)=O FEFCILUKYGHITK-UHFFFAOYSA-N 0.000 description 1
- 239000004604 Blowing Agent Substances 0.000 description 1
- ZVFDTKUVRCTHQE-UHFFFAOYSA-N Diisodecyl phthalate Chemical compound CC(C)CCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC(C)C ZVFDTKUVRCTHQE-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- KRADHMIOFJQKEZ-UHFFFAOYSA-N Tri-2-ethylhexyl trimellitate Chemical compound CCCCC(CC)COC(=O)C1=CC=C(C(=O)OCC(CC)CCCC)C(C(=O)OCC(CC)CCCC)=C1 KRADHMIOFJQKEZ-UHFFFAOYSA-N 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000005250 alkyl acrylate group Chemical group 0.000 description 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
- 238000012662 bulk polymerization Methods 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 150000001993 dienes Chemical class 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000007720 emulsion polymerization reaction Methods 0.000 description 1
- 125000004185 ester group Chemical group 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 238000005469 granulation Methods 0.000 description 1
- 230000003179 granulation Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 230000002035 prolonged effect Effects 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
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 230000003014 reinforcing effect Effects 0.000 description 1
- 238000000518 rheometry Methods 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 229920000638 styrene acrylonitrile Polymers 0.000 description 1
- 238000010558 suspension polymerization method Methods 0.000 description 1
- 125000002889 tridecyl 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])[H] 0.000 description 1
- CPYFCVVBZUCVKJ-UHFFFAOYSA-N tridodecyl benzene-1,2,4-tricarboxylate Chemical compound CCCCCCCCCCCCOC(=O)C1=CC=C(C(=O)OCCCCCCCCCCCC)C(C(=O)OCCCCCCCCCCCC)=C1 CPYFCVVBZUCVKJ-UHFFFAOYSA-N 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/10—Esters; Ether-esters
- C08K5/12—Esters; Ether-esters of cyclic polycarboxylic acids
-
- 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
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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US43685789A | 1989-11-14 | 1989-11-14 | |
| US436,857 | 1989-11-14 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2044176A1 true CA2044176A1 (fr) | 1991-05-15 |
Family
ID=23734111
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002044176A Abandoned CA2044176A1 (fr) | 1989-11-14 | 1990-09-19 | Copolymeres plastifies de triester de composes aromatiques et d'acrylonitrile et de styrene |
Country Status (6)
| Country | Link |
|---|---|
| EP (1) | EP0453524A4 (fr) |
| JP (1) | JPH04503083A (fr) |
| KR (1) | KR920701346A (fr) |
| AU (1) | AU6447390A (fr) |
| CA (1) | CA2044176A1 (fr) |
| WO (1) | WO1991007459A1 (fr) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19737793C1 (de) | 1997-08-29 | 1998-12-24 | Rwe Dea Ag | Ester aromatischer Polycarbonsäuren mit 2-Alkylalkan-1-olen und deren Verwendung |
| US9307679B2 (en) | 2011-03-15 | 2016-04-05 | Kabushiki Kaisha Toshiba | Server room managing air conditioning system |
| ES2648806T3 (es) | 2015-09-28 | 2018-01-08 | Evonik Degussa Gmbh | Éster tripentílico del ácido trimelítico |
| JP7641976B2 (ja) | 2020-09-25 | 2025-03-07 | デンカ株式会社 | 樹脂組成物 |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3280063A (en) * | 1961-03-29 | 1966-10-18 | Borden Co | Esters of a monohydric aliphatic alcohol having 10-20 carbon atoms with a mononuclear aromatic acid having 3-6 carboxy groups as flow promoters for sound record compositions |
| US4654390A (en) * | 1984-08-10 | 1987-03-31 | The Dow Chemical Company | Monomeric plasticizers for halogen-containing resins |
-
1990
- 1990-09-19 KR KR1019910700734A patent/KR920701346A/ko not_active Withdrawn
- 1990-09-19 CA CA002044176A patent/CA2044176A1/fr not_active Abandoned
- 1990-09-19 WO PCT/US1990/005333 patent/WO1991007459A1/fr not_active Ceased
- 1990-09-19 AU AU64473/90A patent/AU6447390A/en not_active Abandoned
- 1990-09-19 EP EP19900914568 patent/EP0453524A4/en not_active Withdrawn
- 1990-09-19 JP JP2513792A patent/JPH04503083A/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| KR920701346A (ko) | 1992-08-11 |
| EP0453524A4 (en) | 1992-05-13 |
| WO1991007459A1 (fr) | 1991-05-30 |
| JPH04503083A (ja) | 1992-06-04 |
| EP0453524A1 (fr) | 1991-10-30 |
| AU6447390A (en) | 1991-06-13 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FZDE | Dead |