CA2289567A1 - Blends of ethylene-vinyl acetate copolymers and ethylene-vinyl acetate-carbon monoxide terpolymers - Google Patents
Blends of ethylene-vinyl acetate copolymers and ethylene-vinyl acetate-carbon monoxide terpolymers Download PDFInfo
- Publication number
- CA2289567A1 CA2289567A1 CA002289567A CA2289567A CA2289567A1 CA 2289567 A1 CA2289567 A1 CA 2289567A1 CA 002289567 A CA002289567 A CA 002289567A CA 2289567 A CA2289567 A CA 2289567A CA 2289567 A1 CA2289567 A1 CA 2289567A1
- Authority
- CA
- Canada
- Prior art keywords
- vinyl acetate
- ethylene
- percentage
- mfi
- carbon monoxide
- 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
- 239000000203 mixture Substances 0.000 title claims abstract description 100
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 title claims abstract description 28
- 229920001897 terpolymer Polymers 0.000 title claims abstract description 22
- 229920002554 vinyl polymer Polymers 0.000 title claims description 16
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical group CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims abstract description 40
- 239000005038 ethylene vinyl acetate Substances 0.000 claims abstract description 19
- 239000000546 pharmaceutical excipient Substances 0.000 claims abstract description 14
- 229920001577 copolymer Polymers 0.000 claims abstract description 9
- 229910002091 carbon monoxide Inorganic materials 0.000 claims description 19
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 claims description 15
- 238000000034 method Methods 0.000 claims description 13
- 239000003063 flame retardant Substances 0.000 claims description 11
- 239000003963 antioxidant agent Substances 0.000 claims description 9
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 claims description 8
- 229910052736 halogen Inorganic materials 0.000 claims description 8
- 150000002367 halogens Chemical class 0.000 claims description 8
- 239000000155 melt Substances 0.000 claims description 8
- 238000002156 mixing Methods 0.000 claims description 8
- 239000007822 coupling agent Substances 0.000 claims description 7
- 239000003431 cross linking reagent Substances 0.000 claims description 7
- 230000003078 antioxidant effect Effects 0.000 claims description 6
- 230000008569 process Effects 0.000 claims description 6
- 239000000945 filler Substances 0.000 claims description 5
- 239000008188 pellet Substances 0.000 claims description 5
- 239000004614 Process Aid Substances 0.000 claims description 4
- SQYFAXDCJCWIOT-UHFFFAOYSA-N carbon monoxide;ethene;ethenyl acetate Chemical compound O=[C].C=C.CC(=O)OC=C SQYFAXDCJCWIOT-UHFFFAOYSA-N 0.000 claims description 4
- 229920010346 Very Low Density Polyethylene (VLDPE) Polymers 0.000 claims 4
- 239000006057 Non-nutritive feed additive Substances 0.000 claims 3
- 239000000049 pigment Substances 0.000 claims 3
- 239000004615 ingredient Substances 0.000 abstract description 12
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 abstract description 5
- 239000005977 Ethylene Substances 0.000 abstract description 5
- 235000021355 Stearic acid Nutrition 0.000 abstract description 5
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 abstract description 5
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 abstract description 5
- 239000008117 stearic acid Substances 0.000 abstract description 5
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 abstract description 2
- RREGISFBPQOLTM-UHFFFAOYSA-N alumane;trihydrate Chemical compound O.O.O.[AlH3] RREGISFBPQOLTM-UHFFFAOYSA-N 0.000 abstract description 2
- 239000006229 carbon black Substances 0.000 abstract description 2
- WOXXJEVNDJOOLV-UHFFFAOYSA-N ethenyl-tris(2-methoxyethoxy)silane Chemical compound COCCO[Si](OCCOC)(OCCOC)C=C WOXXJEVNDJOOLV-UHFFFAOYSA-N 0.000 abstract 1
- 229920003345 Elvax® Polymers 0.000 description 22
- 230000000717 retained effect Effects 0.000 description 17
- 230000000704 physical effect Effects 0.000 description 16
- 229940105305 carbon monoxide Drugs 0.000 description 14
- 150000001875 compounds Chemical class 0.000 description 12
- 239000000463 material Substances 0.000 description 11
- 229920000642 polymer Polymers 0.000 description 10
- 229920003314 Elvaloy® Polymers 0.000 description 9
- 239000000654 additive Substances 0.000 description 7
- MXRIRQGCELJRSN-UHFFFAOYSA-N O.O.O.[Al] Chemical compound O.O.O.[Al] MXRIRQGCELJRSN-UHFFFAOYSA-N 0.000 description 6
- BGYHLZZASRKEJE-UHFFFAOYSA-N [3-[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxy]-2,2-bis[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxymethyl]propyl] 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)OCC(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 BGYHLZZASRKEJE-UHFFFAOYSA-N 0.000 description 6
- DQXBYHZEEUGOBF-UHFFFAOYSA-N but-3-enoic acid;ethene Chemical compound C=C.OC(=O)CC=C DQXBYHZEEUGOBF-UHFFFAOYSA-N 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- 229920003346 Levapren® Polymers 0.000 description 5
- 238000004132 cross linking Methods 0.000 description 5
- 229920001038 ethylene copolymer Polymers 0.000 description 5
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 4
- 230000008901 benefit Effects 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 238000010410 dusting Methods 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- 229910000077 silane Inorganic materials 0.000 description 4
- 239000000779 smoke Substances 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 3
- HDERJYVLTPVNRI-UHFFFAOYSA-N ethene;ethenyl acetate Chemical group C=C.CC(=O)OC=C HDERJYVLTPVNRI-UHFFFAOYSA-N 0.000 description 3
- 230000005484 gravity Effects 0.000 description 3
- 230000001965 increasing effect Effects 0.000 description 3
- 150000002978 peroxides Chemical class 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 238000010998 test method Methods 0.000 description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000012764 mineral filler Substances 0.000 description 2
- WTEVQBCEXWBHNA-YFHOEESVSA-N neral Chemical compound CC(C)=CCC\C(C)=C/C=O WTEVQBCEXWBHNA-YFHOEESVSA-N 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 239000002243 precursor Substances 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- IPJGAEWUPXWFPL-UHFFFAOYSA-N 1-[3-(2,5-dioxopyrrol-1-yl)phenyl]pyrrole-2,5-dione Chemical compound O=C1C=CC(=O)N1C1=CC=CC(N2C(C=CC2=O)=O)=C1 IPJGAEWUPXWFPL-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- WTEVQBCEXWBHNA-UHFFFAOYSA-N Citral Natural products CC(C)=CCCC(C)=CC=O WTEVQBCEXWBHNA-UHFFFAOYSA-N 0.000 description 1
- 206010010071 Coma Diseases 0.000 description 1
- OWYWGLHRNBIFJP-UHFFFAOYSA-N Ipazine Chemical compound CCN(CC)C1=NC(Cl)=NC(NC(C)C)=N1 OWYWGLHRNBIFJP-UHFFFAOYSA-N 0.000 description 1
- NJIWVMGUAFXONX-UHFFFAOYSA-J [C+4].CC([O-])=O.CC([O-])=O.CC([O-])=O.CC([O-])=O Chemical compound [C+4].CC([O-])=O.CC([O-])=O.CC([O-])=O.CC([O-])=O NJIWVMGUAFXONX-UHFFFAOYSA-J 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- WTEVQBCEXWBHNA-JXMROGBWSA-N citral A Natural products CC(C)=CCC\C(C)=C\C=O WTEVQBCEXWBHNA-JXMROGBWSA-N 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 230000003292 diminished effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000013020 final formulation Substances 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000003348 petrochemical agent Substances 0.000 description 1
- 230000036314 physical performance Effects 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 238000000518 rheometry Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- ORGHESHFQPYLAO-UHFFFAOYSA-N vinyl radical Chemical class C=[CH] ORGHESHFQPYLAO-UHFFFAOYSA-N 0.000 description 1
- UKRDPEFKFJNXQM-UHFFFAOYSA-N vinylsilane Chemical compound [SiH3]C=C UKRDPEFKFJNXQM-UHFFFAOYSA-N 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
- 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
- C08L23/04—Homopolymers or copolymers of ethene
- C08L23/08—Copolymers of ethene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/02—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
-
- 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
- C08L23/04—Homopolymers or copolymers of ethene
- C08L23/08—Copolymers of ethene
- C08L23/0846—Copolymers of ethene with unsaturated hydrocarbons containing atoms other than carbon or hydrogen
- C08L23/0853—Ethene vinyl acetate copolymers
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 Insulating Materials (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US4972497P | 1997-06-17 | 1997-06-17 | |
| US60/049,724 | 1997-06-17 | ||
| US09/095,810 US6133367A (en) | 1997-06-17 | 1998-06-11 | Ethylene vinyl acetate blends |
| US09/095,810 | 1998-06-11 | ||
| PCT/US1998/012360 WO1998058019A1 (en) | 1997-06-17 | 1998-06-12 | Blends of ethylene-vinyl acetate copolymers and ethylene-vinyl acetate-carbon monoxide terpolymers |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2289567A1 true CA2289567A1 (en) | 1998-12-23 |
Family
ID=26727466
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002289567A Abandoned CA2289567A1 (en) | 1997-06-17 | 1998-06-12 | Blends of ethylene-vinyl acetate copolymers and ethylene-vinyl acetate-carbon monoxide terpolymers |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US6133367A (enExample) |
| EP (1) | EP0991717B1 (enExample) |
| JP (1) | JP4159118B2 (enExample) |
| CA (1) | CA2289567A1 (enExample) |
| DE (1) | DE69838675T2 (enExample) |
| WO (1) | WO1998058019A1 (enExample) |
Families Citing this family (26)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6608136B1 (en) | 1999-07-26 | 2003-08-19 | E. I. Du Pont De Nemours And Company | Polyphenylene sulfide alloy composition |
| JP2002042921A (ja) * | 2000-04-18 | 2002-02-08 | Nitto Denko Corp | 異方導電性フィルムの製造方法及び異方導電性フィルム |
| US6645623B2 (en) | 2000-07-20 | 2003-11-11 | E. I. Du Pont De Nemours And Company | Polyphenylene sulfide alloy coated wire |
| US6805956B2 (en) | 2000-07-20 | 2004-10-19 | E.I. Du Pont De Nemours And Company | Process for coating a wire or cable with polyphenylene sulfide alloy and resulting coated wire |
| US6274066B1 (en) * | 2000-10-11 | 2001-08-14 | General Cable Technologies Corporation | Low adhesion semi-conductive electrical shields |
| US6392154B1 (en) * | 2001-04-04 | 2002-05-21 | Equistar Chemicals, Lp | Fast curing polymer composition |
| US20050020777A1 (en) * | 2003-07-23 | 2005-01-27 | Breese David Ryan | Ethylene-vinyl acetate compositions having improved heat seal properties |
| US20060172143A1 (en) * | 2003-07-23 | 2006-08-03 | Breese David R | Extrusion coating process and coated substrates having improved heat seal properties |
| US20060263556A1 (en) * | 2003-09-15 | 2006-11-23 | Dayco Products, Llc | Elastomer compositions for use in a hydrocarbon resistant hose |
| US20050059763A1 (en) * | 2003-09-15 | 2005-03-17 | Beck Harold D. | Elastomer compositions for use in a hydrocarbon resistant hose |
| US20050058795A1 (en) * | 2003-09-15 | 2005-03-17 | Beck Harold D. | Vinyl ester hose and method for manufacture of such hose |
| US8394896B2 (en) * | 2004-12-06 | 2013-03-12 | Lanxess Inc. | Liquid α-olefin vinyl acetate compounds |
| DK2115093T3 (da) * | 2006-12-15 | 2011-10-17 | Prysmian Spa | Energitransmissionskabel |
| RU2420555C2 (ru) * | 2006-12-15 | 2011-06-10 | Призмиан С.П.А. | Энергопередающий кабель |
| ES2375816T3 (es) * | 2009-03-16 | 2012-03-06 | Trelleborg Forsheda Building Ab | Cable de media tensión. |
| US8287770B2 (en) * | 2010-03-05 | 2012-10-16 | General Cable Technologies Corporation | Semiconducting composition |
| US8779061B2 (en) * | 2011-10-26 | 2014-07-15 | E I Du Pont De Nemours And Company | Curable elastomeric compositions |
| JP5821827B2 (ja) * | 2012-11-20 | 2015-11-24 | 日立金属株式会社 | ノンハロゲン架橋樹脂組成物を用いた鉄道車両用絶縁電線、鉄道車両用ケーブル |
| FR3000832B1 (fr) * | 2013-01-07 | 2016-08-12 | Nexans | Cable electrique comprenant une couche polymerique facilement pelable |
| US8913862B1 (en) * | 2013-09-27 | 2014-12-16 | Corning Optical Communications LLC | Optical communication cable |
| CA2900919C (en) | 2014-08-18 | 2018-09-11 | Congoleum Corporation | Resilient articles and methods of manufacturing thereof |
| CN107236166B (zh) * | 2015-05-11 | 2020-12-29 | 中广核高新核材科技(苏州)有限公司 | 用于石油平台的低烟无卤辐照交联耐泥浆阻燃电缆料的制备工艺 |
| DK3216831T4 (da) | 2016-03-08 | 2022-12-19 | S A Imperbel N V | Vandtætningsmembransammensætning |
| WO2017180679A1 (en) | 2016-04-12 | 2017-10-19 | The Sherwin-Williams Company | Alkene vinyl alkanoate copolymers and polymerization methods therefor |
| EP3547331B1 (en) * | 2018-03-28 | 2022-03-16 | General Cable Technologies Corporation | Fire resistant data communication cable |
| US20220403151A1 (en) * | 2019-08-28 | 2022-12-22 | Dow Global Technologies Llc | Polyethylene copolymer blend |
Family Cites Families (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4191798A (en) * | 1978-11-22 | 1980-03-04 | E. I. Du Pont De Nemours And Company | Highly filled thermoplastic compositions based on ethylene interpolymers and processing oils |
| US4403007A (en) * | 1980-08-11 | 1983-09-06 | E. I. Du Pont De Nemours & Co. | Filled thermoplastic compositions based on ethylene interpolymers and polyester, polyether and polyether ester plasticizers |
| US4338227A (en) * | 1980-09-05 | 1982-07-06 | E. I. Du Pont De Nemours And Company | Ethylene copolymer blends and adhesives based thereon |
| US4510281A (en) * | 1981-05-26 | 1985-04-09 | E. I. Du Pont De Nemours And Company | Tack-free polymer pellets |
| US4520169A (en) * | 1982-09-02 | 1985-05-28 | E. I. Du Pont De Nemours And Company | Elastomeric sol/gel blends |
| EP0135027B1 (en) * | 1983-07-22 | 1989-02-08 | Du Pont-Mitsui Polychemicals Co., Ltd. | Polymer composition |
| US4910253A (en) * | 1986-07-10 | 1990-03-20 | The Dow Chemical Company | Oxygen barrier resins |
| US5276082A (en) * | 1990-07-13 | 1994-01-04 | Armstrong World Industries, Inc. | Halogen-free floor covering |
| US5470657A (en) * | 1991-04-26 | 1995-11-28 | Sumitomo Electric Industries, Ltd. | Heat-resistant, high-voltage lead wire for direct current |
| DE4124560A1 (de) * | 1991-07-24 | 1993-01-28 | Wacker Chemie Gmbh | Beschichtungsmittel zur herstellung von wasserdichten, dampfdurchlaessigen und flammverzoegernden beschichtungen |
| CA2161953A1 (en) * | 1993-05-04 | 1994-11-10 | Edward J. Deyrup | Improved bonding resin and methods relating thereto |
| JP3423365B2 (ja) * | 1993-08-02 | 2003-07-07 | 古河電気工業株式会社 | 連続気泡型樹脂発泡体製造用組成物 |
| US5475041A (en) * | 1993-10-12 | 1995-12-12 | Polytechnic University | Flame retardant polyolefin wire and cable insulation |
| US5461110A (en) * | 1994-05-04 | 1995-10-24 | Du Pont Canada Inc. | Cross-linkable adhesive polymers |
| EP0775051A4 (en) * | 1994-08-10 | 1997-11-19 | Du Pont | PACKING LAYER FOR PACKAGING |
| EP0703271A1 (en) * | 1994-09-22 | 1996-03-27 | Du Pont De Nemours International S.A. | Flexible nonhalogen containing thermoplastic polyolefin compositions |
-
1998
- 1998-06-11 US US09/095,810 patent/US6133367A/en not_active Expired - Lifetime
- 1998-06-12 WO PCT/US1998/012360 patent/WO1998058019A1/en not_active Ceased
- 1998-06-12 CA CA002289567A patent/CA2289567A1/en not_active Abandoned
- 1998-06-12 JP JP50461799A patent/JP4159118B2/ja not_active Expired - Fee Related
- 1998-06-12 EP EP98929061A patent/EP0991717B1/en not_active Expired - Lifetime
- 1998-06-12 DE DE69838675T patent/DE69838675T2/de not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| DE69838675T2 (de) | 2008-08-28 |
| DE69838675D1 (de) | 2007-12-20 |
| EP0991717B1 (en) | 2007-11-07 |
| JP2002514262A (ja) | 2002-05-14 |
| US6133367A (en) | 2000-10-17 |
| WO1998058019A1 (en) | 1998-12-23 |
| EP0991717A1 (en) | 2000-04-12 |
| JP4159118B2 (ja) | 2008-10-01 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FZDE | Dead |