ES2204383T3 - Polimeros fluorados modificados reticulables. - Google Patents
Polimeros fluorados modificados reticulables.Info
- Publication number
- ES2204383T3 ES2204383T3 ES00105117T ES00105117T ES2204383T3 ES 2204383 T3 ES2204383 T3 ES 2204383T3 ES 00105117 T ES00105117 T ES 00105117T ES 00105117 T ES00105117 T ES 00105117T ES 2204383 T3 ES2204383 T3 ES 2204383T3
- Authority
- ES
- Spain
- Prior art keywords
- polymer
- copolymers
- procedure
- thermoprocessable
- crosslinking agents
- 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.)
- Expired - Lifetime
Links
- 229920000642 polymer Polymers 0.000 title claims description 88
- 239000000203 mixture Substances 0.000 claims abstract description 33
- UUAGAQFQZIEFAH-UHFFFAOYSA-N chlorotrifluoroethylene Chemical group FC(F)=C(F)Cl UUAGAQFQZIEFAH-UHFFFAOYSA-N 0.000 claims abstract description 29
- 229920001577 copolymer Polymers 0.000 claims abstract description 25
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 claims abstract description 22
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims abstract description 17
- 239000005977 Ethylene Substances 0.000 claims abstract description 17
- 239000000178 monomer Substances 0.000 claims abstract description 17
- 239000003431 cross linking reagent Substances 0.000 claims abstract description 15
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims abstract description 11
- -1 C1-C20 Chemical group 0.000 claims abstract description 10
- 150000002148 esters Chemical class 0.000 claims abstract description 7
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims abstract description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 3
- 125000000753 cycloalkyl group Chemical group 0.000 claims abstract description 3
- 125000000524 functional group Chemical group 0.000 claims abstract description 3
- 125000005842 heteroatom Chemical group 0.000 claims abstract description 3
- 125000000896 monocarboxylic acid group Chemical group 0.000 claims abstract description 3
- 150000002118 epoxides Chemical class 0.000 claims abstract 2
- 238000000034 method Methods 0.000 claims description 23
- KOMNUTZXSVSERR-UHFFFAOYSA-N 1,3,5-tris(prop-2-enyl)-1,3,5-triazinane-2,4,6-trione Chemical compound C=CCN1C(=O)N(CC=C)C(=O)N(CC=C)C1=O KOMNUTZXSVSERR-UHFFFAOYSA-N 0.000 claims description 13
- 238000004132 cross linking Methods 0.000 claims description 8
- BJELTSYBAHKXRW-UHFFFAOYSA-N 2,4,6-triallyloxy-1,3,5-triazine Chemical compound C=CCOC1=NC(OCC=C)=NC(OCC=C)=N1 BJELTSYBAHKXRW-UHFFFAOYSA-N 0.000 claims description 6
- 125000003118 aryl group Chemical group 0.000 claims description 6
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 5
- 238000010438 heat treatment Methods 0.000 claims description 5
- HDIHOAXFFROQHR-UHFFFAOYSA-N 6-aminohexylcarbamic acid Chemical compound NCCCCCCNC(O)=O HDIHOAXFFROQHR-UHFFFAOYSA-N 0.000 claims description 4
- 229930185605 Bisphenol Natural products 0.000 claims description 4
- 239000003795 chemical substances by application Substances 0.000 claims description 4
- ATPFMBHTMKBVLS-VZEWWGGESA-N (z)-3-phenyl-n-[6-[[(e)-3-phenylprop-2-enylidene]amino]hexyl]prop-2-en-1-imine Chemical compound C=1C=CC=CC=1/C=C/C=NCCCCCCN=C\C=C/C1=CC=CC=C1 ATPFMBHTMKBVLS-VZEWWGGESA-N 0.000 claims description 3
- ROLAGNYPWIVYTG-UHFFFAOYSA-N 1,2-bis(4-methoxyphenyl)ethanamine;hydrochloride Chemical compound Cl.C1=CC(OC)=CC=C1CC(N)C1=CC=C(OC)C=C1 ROLAGNYPWIVYTG-UHFFFAOYSA-N 0.000 claims description 3
- 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 claims description 3
- XSQHUYDRSDBCHN-UHFFFAOYSA-N 2,3-dimethyl-2-propan-2-ylbutanenitrile Chemical compound CC(C)C(C)(C#N)C(C)C XSQHUYDRSDBCHN-UHFFFAOYSA-N 0.000 claims description 3
- 150000003923 2,5-pyrrolediones Chemical class 0.000 claims description 3
- PDFSXHZXNZCKNF-UHFFFAOYSA-N 3,3,4,4,5,5,6,6,7,7,8,8-dodecafluorodeca-1,9-diene Chemical compound C=CC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C=C PDFSXHZXNZCKNF-UHFFFAOYSA-N 0.000 claims description 3
- VPWNQTHUCYMVMZ-UHFFFAOYSA-N 4,4'-sulfonyldiphenol Chemical class C1=CC(O)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 VPWNQTHUCYMVMZ-UHFFFAOYSA-N 0.000 claims description 3
- 239000004971 Cross linker Substances 0.000 claims description 3
- 239000002253 acid Substances 0.000 claims description 3
- ZDNFTNPFYCKVTB-UHFFFAOYSA-N bis(prop-2-enyl) benzene-1,4-dicarboxylate Chemical compound C=CCOC(=O)C1=CC=C(C(=O)OCC=C)C=C1 ZDNFTNPFYCKVTB-UHFFFAOYSA-N 0.000 claims description 3
- PXORBAGTGTXORO-UHFFFAOYSA-N 1-phenyl-1h-indene Chemical compound C1=CC2=CC=CC=C2C1C1=CC=CC=C1 PXORBAGTGTXORO-UHFFFAOYSA-N 0.000 claims description 2
- 238000002156 mixing Methods 0.000 claims description 2
- 125000001931 aliphatic group Chemical group 0.000 claims 1
- 150000004984 aromatic diamines Chemical class 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 description 13
- 229920001971 elastomer Polymers 0.000 description 11
- 239000000446 fuel Substances 0.000 description 10
- 229920000459 Nitrile rubber Polymers 0.000 description 8
- 239000000047 product Substances 0.000 description 8
- 229920002313 fluoropolymer Polymers 0.000 description 7
- 239000005060 rubber Substances 0.000 description 7
- 239000004952 Polyamide Substances 0.000 description 6
- 230000035699 permeability Effects 0.000 description 6
- 229920002647 polyamide Polymers 0.000 description 6
- YFZCNXJOYHYIGC-UHFFFAOYSA-N (2,2,2-trichloroacetyl) 2,2,2-trichloroethaneperoxoate Chemical compound ClC(Cl)(Cl)C(=O)OOC(=O)C(Cl)(Cl)Cl YFZCNXJOYHYIGC-UHFFFAOYSA-N 0.000 description 5
- 238000006116 polymerization reaction Methods 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- 238000007906 compression Methods 0.000 description 4
- 230000006835 compression Effects 0.000 description 4
- 239000000806 elastomer Substances 0.000 description 4
- 239000003999 initiator Substances 0.000 description 4
- GDOPTJXRTPNYNR-UHFFFAOYSA-N methylcyclopentane Chemical compound CC1CCCC1 GDOPTJXRTPNYNR-UHFFFAOYSA-N 0.000 description 4
- 229920001169 thermoplastic Polymers 0.000 description 4
- 239000004416 thermosoftening plastic Substances 0.000 description 4
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 230000001070 adhesive effect Effects 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- 229920005558 epichlorohydrin rubber Polymers 0.000 description 3
- 229910000856 hastalloy Inorganic materials 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 229920000728 polyester Polymers 0.000 description 3
- BQCIDUSAKPWEOX-UHFFFAOYSA-N 1,1-Difluoroethene Chemical compound FC(F)=C BQCIDUSAKPWEOX-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- NHTMVDHEPJAVLT-UHFFFAOYSA-N Isooctane Chemical compound CC(C)CC(C)(C)C NHTMVDHEPJAVLT-UHFFFAOYSA-N 0.000 description 2
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 229920000299 Nylon 12 Polymers 0.000 description 2
- WAIPAZQMEIHHTJ-UHFFFAOYSA-N [Cr].[Co] Chemical compound [Cr].[Co] WAIPAZQMEIHHTJ-UHFFFAOYSA-N 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- JVSWJIKNEAIKJW-UHFFFAOYSA-N dimethyl-hexane Natural products CCCCCC(C)C JVSWJIKNEAIKJW-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 229920000098 polyolefin Polymers 0.000 description 2
- 239000004800 polyvinyl chloride Substances 0.000 description 2
- 230000005855 radiation Effects 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000003017 thermal stabilizer Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- YHMYGUUIMTVXNW-UHFFFAOYSA-N 1,3-dihydrobenzimidazole-2-thione Chemical compound C1=CC=C2NC(S)=NC2=C1 YHMYGUUIMTVXNW-UHFFFAOYSA-N 0.000 description 1
- OWRCNXZUPFZXOS-UHFFFAOYSA-N 1,3-diphenylguanidine Chemical compound C=1C=CC=CC=1NC(=N)NC1=CC=CC=C1 OWRCNXZUPFZXOS-UHFFFAOYSA-N 0.000 description 1
- VNAFWALXWOAPCK-UHFFFAOYSA-N 1-phenyl-2,3-dihydro-1h-indene Chemical class C1CC2=CC=CC=C2C1C1=CC=CC=C1 VNAFWALXWOAPCK-UHFFFAOYSA-N 0.000 description 1
- XMNIXWIUMCBBBL-UHFFFAOYSA-N 2-(2-phenylpropan-2-ylperoxy)propan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)OOC(C)(C)C1=CC=CC=C1 XMNIXWIUMCBBBL-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- 229920001780 ECTFE Polymers 0.000 description 1
- 229920002943 EPDM rubber Polymers 0.000 description 1
- JHWNWJKBPDFINM-UHFFFAOYSA-N Laurolactam Chemical compound O=C1CCCCCCCCCCCN1 JHWNWJKBPDFINM-UHFFFAOYSA-N 0.000 description 1
- 206010024453 Ligament sprain Diseases 0.000 description 1
- 229920000571 Nylon 11 Polymers 0.000 description 1
- 229920002292 Nylon 6 Polymers 0.000 description 1
- 229920002302 Nylon 6,6 Polymers 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 208000010040 Sprains and Strains Diseases 0.000 description 1
- 229920006172 Tetrafluoroethylene propylene Polymers 0.000 description 1
- 229920000800 acrylic rubber Polymers 0.000 description 1
- 229920006397 acrylic thermoplastic Polymers 0.000 description 1
- BPMXVYBQJXDTGH-UHFFFAOYSA-N benzyl-(diethylamino)-diphenylphosphanium Chemical compound C=1C=CC=CC=1[P+](C=1C=CC=CC=1)(N(CC)CC)CC1=CC=CC=C1 BPMXVYBQJXDTGH-UHFFFAOYSA-N 0.000 description 1
- XAUGYNZHGJOSSQ-UHFFFAOYSA-N bis(2-butoxy-2-ethoxyethyl) hexanedioate Chemical compound CCCCOC(OCC)COC(=O)CCCCC(=O)OCC(OCC)OCCCC XAUGYNZHGJOSSQ-UHFFFAOYSA-N 0.000 description 1
- SCABKEBYDRTODC-UHFFFAOYSA-N bis[2-(2-butoxyethoxy)ethyl] hexanedioate Chemical compound CCCCOCCOCCOC(=O)CCCCC(=O)OCCOCCOCCCC SCABKEBYDRTODC-UHFFFAOYSA-N 0.000 description 1
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 1
- 238000004061 bleaching Methods 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- SZRLKIKBPASKQH-UHFFFAOYSA-M dibutyldithiocarbamate Chemical compound CCCCN(C([S-])=S)CCCC SZRLKIKBPASKQH-UHFFFAOYSA-M 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 description 1
- 229920001038 ethylene copolymer Polymers 0.000 description 1
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 239000000383 hazardous chemical Substances 0.000 description 1
- 229920001903 high density polyethylene Polymers 0.000 description 1
- 239000004700 high-density polyethylene Substances 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229920001684 low density polyethylene Polymers 0.000 description 1
- 239000004702 low-density polyethylene Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- QDBQXOAICGSACD-UHFFFAOYSA-N n'-hexylhexanediamide Chemical compound CCCCCCNC(=O)CCCCC(N)=O QDBQXOAICGSACD-UHFFFAOYSA-N 0.000 description 1
- DEQZTKGFXNUBJL-UHFFFAOYSA-N n-(1,3-benzothiazol-2-ylsulfanyl)cyclohexanamine Chemical compound C1CCCCC1NSC1=NC2=CC=CC=C2S1 DEQZTKGFXNUBJL-UHFFFAOYSA-N 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 150000002924 oxiranes Chemical class 0.000 description 1
- 239000012466 permeate Substances 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920002492 poly(sulfone) Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920006122 polyamide resin Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 239000004810 polytetrafluoroethylene Substances 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000000779 smoke Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 1
- 125000006337 tetrafluoro ethyl group Chemical group 0.000 description 1
- GZKYAMPVOJYWJF-UHFFFAOYSA-N toluene;2,2,4-trimethylpentane Chemical compound CC1=CC=CC=C1.CC(C)CC(C)(C)C GZKYAMPVOJYWJF-UHFFFAOYSA-N 0.000 description 1
- 229920002554 vinyl polymer Polymers 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
- C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
- C08K5/0025—Crosslinking or vulcanising agents; including accelerators
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)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
- Laminated Bodies (AREA)
- Graft Or Block Polymers (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| ITMI990549 | 1999-03-19 | ||
| IT1999MI000549A IT1312016B1 (it) | 1999-03-19 | 1999-03-19 | Polimeri fluorurati modificati reticolabili. |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2204383T3 true ES2204383T3 (es) | 2004-05-01 |
Family
ID=11382329
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES00105117T Expired - Lifetime ES2204383T3 (es) | 1999-03-19 | 2000-03-10 | Polimeros fluorados modificados reticulables. |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US6476150B1 (Direct) |
| EP (1) | EP1038914B1 (Direct) |
| JP (1) | JP4650965B2 (Direct) |
| AT (1) | ATE247689T1 (Direct) |
| DE (1) | DE60004587T2 (Direct) |
| ES (1) | ES2204383T3 (Direct) |
| IT (1) | IT1312016B1 (Direct) |
| NO (1) | NO323570B1 (Direct) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IT1312015B1 (it) * | 1999-03-19 | 2002-04-04 | Ausimont Spa | Composizioni reticolate di fluoropolimeri termoplastici. |
| IT1318700B1 (it) * | 2000-09-18 | 2003-08-27 | Ausimont Spa | Composizione multistrato comprendente fluoropolimeri e polimeriidrogenati. |
| IT1318709B1 (it) * | 2000-09-27 | 2003-08-27 | Ausimont Spa | Composizioni termoplastiche di fluoropolimeri. |
| US7320818B2 (en) | 2001-03-13 | 2008-01-22 | Ausimont S.P.A. | Multilayers of polyamides and fluorinated copolymers |
| ITMI20011151A1 (it) | 2001-05-31 | 2002-12-01 | Ausimont Spa | Accoppiati fra poliamidi e cpvc |
| US7029736B2 (en) * | 2003-06-10 | 2006-04-18 | The Goodyear Tire & Rubber Company | Hose construction containing thermoplastic fluoropolymer |
| US9328256B2 (en) * | 2012-04-13 | 2016-05-03 | Xerox Corporation | Reinforced fluoropolymer composites comprising surface functionalized nanocrystalline cellulose |
| GB201318914D0 (en) * | 2013-10-25 | 2013-12-11 | Wellstream Int Ltd | A flexible pipe body |
| JP6327372B2 (ja) * | 2017-02-13 | 2018-05-23 | ダイキン工業株式会社 | 混合粉末、皮膜及び物品 |
| CN109535687B (zh) * | 2018-11-16 | 2021-03-02 | 安徽江山机械有限公司 | 一种不易开裂的环卫垃圾桶 |
| CN109762274A (zh) * | 2019-02-18 | 2019-05-17 | 南通壹选工业设计有限公司 | 抗老化的pvc电缆料 |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3763222A (en) | 1972-04-11 | 1973-10-02 | Itt | Esters of phenyl indan |
| US3840619A (en) | 1972-07-28 | 1974-10-08 | Itt | Polymeric compositions |
| US4039631A (en) * | 1973-01-30 | 1977-08-02 | Allied Chemical Corporation | Radiation cross-linkable compositions of copolymers of ethylene and a halogenated monomer |
| US4121001A (en) | 1977-01-14 | 1978-10-17 | Raychem Corporation | Crosslinking agent for polymers and wire construction utilizing crosslinked polymers |
| FR2494702B1 (fr) * | 1980-11-21 | 1988-03-04 | Srti Soc Rech Tech Ind | Membrane echangeuse d'ions et son procede de fabrication |
| JPH02121206A (ja) * | 1988-10-28 | 1990-05-09 | Hitachi Cable Ltd | 絶縁電線 |
| TW222650B (Direct) * | 1991-04-01 | 1994-04-21 | Dow Corning | |
| JP3134371B2 (ja) * | 1991-07-03 | 2001-02-13 | 東海ゴム工業株式会社 | 樹脂チューブ |
| JPH0725954A (ja) * | 1993-07-09 | 1995-01-27 | Asahi Glass Co Ltd | 接着性弗素ゴムおよびそれを用いた積層体 |
| IT1265460B1 (it) | 1993-12-29 | 1996-11-22 | Ausimont Spa | Elastomeri termoplastici fluorurati dotati di migliorate proprieta' meccaniche ed elastiche, e relativo processo di preparazione |
| US6057014A (en) * | 1995-07-26 | 2000-05-02 | E. I. Du Pont De Nemours And Company | Laminates of composition for improving adhesion of elastomers to polymer compositions |
| JPH10158458A (ja) * | 1996-12-04 | 1998-06-16 | Nippon Zeon Co Ltd | フッ素ゴム組成物 |
| IT1290426B1 (it) * | 1997-03-21 | 1998-12-03 | Ausimont Spa | Polimeri fluorurati termoprocessabili |
| US6239223B1 (en) * | 1997-09-05 | 2001-05-29 | Chemfab Corporation | Fluoropolymeric composition |
| IT1312015B1 (it) * | 1999-03-19 | 2002-04-04 | Ausimont Spa | Composizioni reticolate di fluoropolimeri termoplastici. |
-
1999
- 1999-03-19 IT IT1999MI000549A patent/IT1312016B1/it active
-
2000
- 2000-03-10 AT AT00105117T patent/ATE247689T1/de not_active IP Right Cessation
- 2000-03-10 ES ES00105117T patent/ES2204383T3/es not_active Expired - Lifetime
- 2000-03-10 DE DE60004587T patent/DE60004587T2/de not_active Expired - Lifetime
- 2000-03-10 EP EP00105117A patent/EP1038914B1/en not_active Expired - Lifetime
- 2000-03-16 JP JP2000074323A patent/JP4650965B2/ja not_active Expired - Fee Related
- 2000-03-16 NO NO20001384A patent/NO323570B1/no not_active IP Right Cessation
- 2000-03-17 US US09/528,198 patent/US6476150B1/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| US6476150B1 (en) | 2002-11-05 |
| NO323570B1 (no) | 2007-06-11 |
| EP1038914A1 (en) | 2000-09-27 |
| JP4650965B2 (ja) | 2011-03-16 |
| DE60004587D1 (de) | 2003-09-25 |
| ITMI990549A1 (it) | 2000-09-19 |
| NO20001384D0 (no) | 2000-03-16 |
| DE60004587T2 (de) | 2004-06-24 |
| JP2000313784A (ja) | 2000-11-14 |
| NO20001384L (no) | 2000-09-20 |
| EP1038914B1 (en) | 2003-08-20 |
| ATE247689T1 (de) | 2003-09-15 |
| IT1312016B1 (it) | 2002-04-04 |
| US20020193529A1 (en) | 2002-12-19 |
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