CA2126576A1 - Method for productional thermostable chemical resistant pla stics - Google Patents
Method for productional thermostable chemical resistant pla sticsInfo
- Publication number
- CA2126576A1 CA2126576A1 CA002126576A CA2126576A CA2126576A1 CA 2126576 A1 CA2126576 A1 CA 2126576A1 CA 002126576 A CA002126576 A CA 002126576A CA 2126576 A CA2126576 A CA 2126576A CA 2126576 A1 CA2126576 A1 CA 2126576A1
- Authority
- CA
- Canada
- Prior art keywords
- cross
- resistant
- chemical
- polymer
- glycidylic
- 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
- 238000000034 method Methods 0.000 title claims abstract description 29
- 239000000126 substance Substances 0.000 title claims abstract description 20
- 229920003023 plastic Polymers 0.000 title claims abstract description 16
- 239000004033 plastic Substances 0.000 title claims abstract description 16
- 229920000642 polymer Polymers 0.000 claims abstract description 23
- 229920001577 copolymer Polymers 0.000 claims abstract description 14
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims abstract description 9
- 239000000178 monomer Substances 0.000 claims abstract description 9
- 238000004519 manufacturing process Methods 0.000 claims abstract description 8
- 239000004014 plasticizer Substances 0.000 claims abstract description 7
- 239000003381 stabilizer Substances 0.000 claims abstract description 7
- 239000000463 material Substances 0.000 claims abstract description 5
- 239000000314 lubricant Substances 0.000 claims abstract description 4
- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 claims description 12
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 claims description 9
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 claims description 8
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 6
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 claims description 6
- -1 butyl glycidyl Chemical group 0.000 claims description 6
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 5
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 claims description 5
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 claims description 5
- 230000008569 process Effects 0.000 claims description 5
- RPQRDASANLAFCM-UHFFFAOYSA-N oxiran-2-ylmethyl prop-2-enoate Chemical compound C=CC(=O)OCC1CO1 RPQRDASANLAFCM-UHFFFAOYSA-N 0.000 claims description 4
- FALRKNHUBBKYCC-UHFFFAOYSA-N 2-(chloromethyl)pyridine-3-carbonitrile Chemical compound ClCC1=NC=CC=C1C#N FALRKNHUBBKYCC-UHFFFAOYSA-N 0.000 claims description 3
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 claims description 3
- 150000008065 acid anhydrides Chemical class 0.000 claims description 3
- 239000001361 adipic acid Substances 0.000 claims description 3
- 235000011037 adipic acid Nutrition 0.000 claims description 3
- 150000001408 amides Chemical class 0.000 claims description 3
- 150000001412 amines Chemical class 0.000 claims description 3
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 claims description 3
- 150000001735 carboxylic acids Chemical class 0.000 claims description 3
- 238000007334 copolymerization reaction Methods 0.000 claims description 3
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims description 3
- 235000006408 oxalic acid Nutrition 0.000 claims description 3
- 229940014800 succinic anhydride Drugs 0.000 claims description 3
- 239000004593 Epoxy Substances 0.000 claims description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
- 239000012948 isocyanate Substances 0.000 claims description 2
- 150000002513 isocyanates Chemical class 0.000 claims description 2
- 150000004756 silanes Chemical class 0.000 claims description 2
- 239000003431 cross linking reagent Substances 0.000 claims 5
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 claims 2
- 238000005580 one pot reaction Methods 0.000 claims 1
- 238000003672 processing method Methods 0.000 claims 1
- 239000004971 Cross linker Substances 0.000 abstract description 29
- 239000011888 foil Substances 0.000 abstract description 20
- 238000006243 chemical reaction Methods 0.000 abstract description 9
- 150000002894 organic compounds Chemical class 0.000 abstract 1
- 239000004800 polyvinyl chloride Substances 0.000 description 30
- 229920000915 polyvinyl chloride Polymers 0.000 description 29
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 22
- 238000004132 cross linking Methods 0.000 description 18
- 239000000203 mixture Substances 0.000 description 17
- 238000012360 testing method Methods 0.000 description 17
- 238000003860 storage Methods 0.000 description 11
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 11
- 239000000460 chlorine Substances 0.000 description 8
- 229920001519 homopolymer Polymers 0.000 description 7
- WZRRRFSJFQTGGB-UHFFFAOYSA-N 1,3,5-triazinane-2,4,6-trithione Chemical compound S=C1NC(=S)NC(=S)N1 WZRRRFSJFQTGGB-UHFFFAOYSA-N 0.000 description 5
- 239000000654 additive Substances 0.000 description 4
- 230000009257 reactivity Effects 0.000 description 4
- 238000005096 rolling process Methods 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 230000008901 benefit Effects 0.000 description 3
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 3
- 125000001309 chloro group Chemical group Cl* 0.000 description 3
- 230000007547 defect Effects 0.000 description 3
- HBGGXOJOCNVPFY-UHFFFAOYSA-N diisononyl phthalate Chemical compound CC(C)CCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCC(C)C HBGGXOJOCNVPFY-UHFFFAOYSA-N 0.000 description 3
- 235000019198 oils Nutrition 0.000 description 3
- 238000003825 pressing Methods 0.000 description 3
- IXDGHAZCSMVIFX-UHFFFAOYSA-N 6-(dibutylamino)-1h-1,3,5-triazine-2,4-dithione Chemical compound CCCCN(CCCC)C1=NC(=S)NC(=S)N1 IXDGHAZCSMVIFX-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 229920008712 Copo Polymers 0.000 description 2
- 102100035474 DNA polymerase kappa Human genes 0.000 description 2
- 101710108091 DNA polymerase kappa Proteins 0.000 description 2
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 230000000593 degrading effect Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 125000003700 epoxy group Chemical group 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 150000002500 ions Chemical class 0.000 description 2
- 239000012038 nucleophile Substances 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 150000003254 radicals Chemical class 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 235000012424 soybean oil Nutrition 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- BSYNRYMUTXBXSQ-UHFFFAOYSA-N Aspirin Chemical compound CC(=O)OC1=CC=CC=C1C(O)=O BSYNRYMUTXBXSQ-UHFFFAOYSA-N 0.000 description 1
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- 206010073306 Exposure to radiation Diseases 0.000 description 1
- 239000002841 Lewis acid Substances 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- MFLCLMHBOLWTHH-UHFFFAOYSA-N Panial Natural products COc1ccc2C=CC(=O)Oc2c1C(O)C=C(/C)C=O MFLCLMHBOLWTHH-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- 230000002745 absorbent Effects 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 125000000746 allylic group Chemical group 0.000 description 1
- 238000012662 bulk polymerization Methods 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000007720 emulsion polymerization reaction Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 150000007517 lewis acids Chemical class 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
- 230000000269 nucleophilic effect Effects 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- HCTVWSOKIJULET-LQDWTQKMSA-M phenoxymethylpenicillin potassium Chemical compound [K+].N([C@H]1[C@H]2SC([C@@H](N2C1=O)C([O-])=O)(C)C)C(=O)COC1=CC=CC=C1 HCTVWSOKIJULET-LQDWTQKMSA-M 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 230000008092 positive effect Effects 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 229920013730 reactive polymer Polymers 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000010557 suspension polymerization reaction Methods 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 150000007944 thiolates Chemical class 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- 230000001960 triggered effect Effects 0.000 description 1
- QZQIWEZRSIPYCU-UHFFFAOYSA-N trithiole Chemical compound S1SC=CS1 QZQIWEZRSIPYCU-UHFFFAOYSA-N 0.000 description 1
- 239000013585 weight reducing agent Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/24—Crosslinking, e.g. vulcanising, of macromolecules
-
- 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
- C08F8/00—Chemical modification by after-treatment
- C08F8/34—Introducing sulfur atoms or sulfur-containing groups
-
- 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
- C08F8/00—Chemical modification by after-treatment
- C08F8/46—Reaction with unsaturated dicarboxylic acids or anhydrides thereof, e.g. maleinisation
-
- 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
- C08F2800/00—Copolymer characterised by the proportions of the comonomers expressed
- C08F2800/20—Copolymer characterised by the proportions of the comonomers expressed as weight or mass percentages
-
- 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
- C08F2810/00—Chemical modification of a polymer
- C08F2810/20—Chemical modification of a polymer leading to a crosslinking, either explicitly or inherently
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2327/00—Characterised by the use 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 a halogen; Derivatives of such polymers
- C08J2327/02—Characterised by the use 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 a halogen; Derivatives of such polymers not modified by chemical after-treatment
- C08J2327/04—Characterised by the use 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 a halogen; Derivatives of such polymers not modified by chemical after-treatment containing chlorine atoms
- C08J2327/06—Homopolymers or copolymers of vinyl chloride
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NO915081 | 1991-12-23 | ||
| NO915081A NO175596C (no) | 1991-12-23 | 1991-12-23 | Kjemikalieresistent kryssbundet plast samt fremstilling og anvendelse av denne |
| PCT/NO1992/000194 WO1993013161A1 (en) | 1991-12-23 | 1992-12-09 | Method for productional thermostable chemical resistant plastics |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2126576A1 true CA2126576A1 (en) | 1993-07-08 |
Family
ID=19894709
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002126576A Abandoned CA2126576A1 (en) | 1991-12-23 | 1992-12-09 | Method for productional thermostable chemical resistant pla stics |
Country Status (11)
| Country | Link |
|---|---|
| EP (1) | EP0618938A1 (en, 2012) |
| JP (1) | JPH07502555A (en, 2012) |
| CN (1) | CN1076204A (en, 2012) |
| AU (1) | AU3097492A (en, 2012) |
| CA (1) | CA2126576A1 (en, 2012) |
| FI (1) | FI943023L (en, 2012) |
| HU (1) | HUT68290A (en, 2012) |
| NO (1) | NO175596C (en, 2012) |
| RU (1) | RU94031163A (en, 2012) |
| TW (1) | TW222658B (en, 2012) |
| WO (1) | WO1993013161A1 (en, 2012) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2741083B1 (fr) * | 1995-11-13 | 1999-02-19 | Nobel Plastiques | Procede d'ignifugation d'un composant en matiere plastique appartenant a une installation de distribution d'un liquide inflammable |
| WO1996023656A1 (fr) * | 1995-02-02 | 1996-08-08 | Nobel Plastiques | Procede d'ignifugation d'un composant en matiere plastique appartenant a une installation de distribution d'un liquide inflammable |
| CN106188707A (zh) * | 2015-05-04 | 2016-12-07 | 电气化学工业株式会社 | 氯丁二烯橡胶组合物、硫化成型体及其用途 |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4871801A (en) * | 1988-11-25 | 1989-10-03 | The B. F. Goodrich Company | Reactive polyvinyl chloride and polymer products made therefrom |
| NO166189C (no) * | 1989-02-08 | 1991-06-12 | Norsk Hydro As | Tverrbundet termostabil polymer og fremstilling derav. |
-
1991
- 1991-12-23 NO NO915081A patent/NO175596C/no unknown
-
1992
- 1992-12-09 RU RU94031163/04A patent/RU94031163A/ru unknown
- 1992-12-09 WO PCT/NO1992/000194 patent/WO1993013161A1/en not_active Application Discontinuation
- 1992-12-09 EP EP92924937A patent/EP0618938A1/en not_active Withdrawn
- 1992-12-09 JP JP5511571A patent/JPH07502555A/ja active Pending
- 1992-12-09 CA CA002126576A patent/CA2126576A1/en not_active Abandoned
- 1992-12-09 AU AU30974/92A patent/AU3097492A/en not_active Abandoned
- 1992-12-09 HU HU9401894A patent/HUT68290A/hu unknown
- 1992-12-09 FI FI943023A patent/FI943023L/fi unknown
- 1992-12-23 CN CN92115363.5A patent/CN1076204A/zh active Pending
-
1993
- 1993-01-14 TW TW082100193A patent/TW222658B/zh active
Also Published As
| Publication number | Publication date |
|---|---|
| EP0618938A1 (en) | 1994-10-12 |
| NO175596B (no) | 1994-07-25 |
| FI943023A7 (fi) | 1994-07-27 |
| CN1076204A (zh) | 1993-09-15 |
| TW222658B (en, 2012) | 1994-04-21 |
| FI943023L (fi) | 1994-07-27 |
| FI943023A0 (fi) | 1994-06-22 |
| WO1993013161A1 (en) | 1993-07-08 |
| HUT68290A (en) | 1995-06-28 |
| RU94031163A (ru) | 1996-05-27 |
| JPH07502555A (ja) | 1995-03-16 |
| NO175596C (no) | 1994-11-02 |
| NO915081D0 (no) | 1991-12-23 |
| HU9401894D0 (en) | 1994-09-28 |
| AU3097492A (en) | 1993-07-28 |
| NO915081L (no) | 1993-06-24 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| RU2078775C1 (ru) | Способ получения термостабильного сшитого полимерного материала | |
| US3251817A (en) | Vinylidene chloride copolymer coating compositions | |
| EP0526813B1 (de) | Ethylenpolymerisate enthaltende Polymerlegierungen für flexible Folien | |
| CA2126576A1 (en) | Method for productional thermostable chemical resistant pla stics | |
| US3933771A (en) | Composition of and method of obtaining small particle size polymers and copolymers of vinyl chloride having a fused surface | |
| US3846265A (en) | Production of shaped structures | |
| DE2127840B2 (de) | Härtbare Formpulver | |
| JPH0452296B2 (en, 2012) | ||
| US3723570A (en) | Ethylene-vinyl acetate-allyl glycidyl ether terpolymer with polyvinyl chloride | |
| US2328510A (en) | Dihalo-ethylene copolymerization product | |
| DE2364364B2 (de) | Vernetzbare wäßrige Vinylestercopolymerisatdispersionen | |
| JPH0452297B2 (en, 2012) | ||
| EP0214602B1 (en) | Molding of urethane resin composition | |
| EP0584927B1 (en) | Thermoplastic compositions and processes for cross-linking | |
| US3211676A (en) | Composition comprising polyvinyl chloride and hexamethoxymethyl melamine | |
| US3639365A (en) | Ethylene-vinyl acetate-allyl glycidyl ether terpolymer and plasticized compositions containing same | |
| US4871801A (en) | Reactive polyvinyl chloride and polymer products made therefrom | |
| US3275712A (en) | Production of impact-resistant thermoplastic molding materials | |
| JPS6043374B2 (ja) | 塩化ビニル系樹脂組成物 | |
| US3291862A (en) | Chlorinated polyolefin polymer mixtures | |
| US2855374A (en) | Crotonic acid modified polyvinyl emulsions and process for preparing same | |
| SU1002324A1 (ru) | Наполненна композици на основе поливинилхлорида | |
| JP2634434B2 (ja) | エマルジョン組成物 | |
| US4778841A (en) | Plastic materials for the production of deep-drawn films | |
| EP0609464A1 (en) | Highly water-absorbent fiber |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FZDE | Discontinued |