JP2003530467A5 - - Google Patents
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- JP2003530467A5 JP2003530467A5 JP2001575655A JP2001575655A JP2003530467A5 JP 2003530467 A5 JP2003530467 A5 JP 2003530467A5 JP 2001575655 A JP2001575655 A JP 2001575655A JP 2001575655 A JP2001575655 A JP 2001575655A JP 2003530467 A5 JP2003530467 A5 JP 2003530467A5
- Authority
- JP
- Japan
- Prior art keywords
- polymer
- carbon
- hydrogenation
- double bonds
- acid
- 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.)
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- 229920000642 polymer Polymers 0.000 description 41
- 238000000034 method Methods 0.000 description 25
- 238000005984 hydrogenation reaction Methods 0.000 description 19
- 150000001875 compounds Chemical class 0.000 description 15
- 239000011203 carbon fibre reinforced carbon Substances 0.000 description 12
- 150000002825 nitriles Chemical class 0.000 description 10
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 8
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 8
- 150000001993 dienes Chemical class 0.000 description 8
- 239000003446 ligand Substances 0.000 description 7
- 229910052703 rhodium Inorganic materials 0.000 description 7
- 239000010948 rhodium Substances 0.000 description 7
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 7
- 229920000126 latex Polymers 0.000 description 6
- 239000002253 acid Substances 0.000 description 5
- 239000004816 latex Substances 0.000 description 5
- 150000001735 carboxylic acids Chemical class 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 239000003960 organic solvent Substances 0.000 description 4
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 3
- 238000005033 Fourier transform infrared spectroscopy Methods 0.000 description 3
- 229920000459 Nitrile rubber Polymers 0.000 description 3
- 239000004952 Polyamide Substances 0.000 description 3
- 239000003426 co-catalyst Substances 0.000 description 3
- 239000003995 emulsifying agent Substances 0.000 description 3
- 229920006168 hydrated nitrile rubber Polymers 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 125000002560 nitrile group Chemical group 0.000 description 3
- 229920002647 polyamide Polymers 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- PMJHHCWVYXUKFD-SNAWJCMRSA-N (E)-1,3-pentadiene Chemical compound C\C=C\C=C PMJHHCWVYXUKFD-SNAWJCMRSA-N 0.000 description 2
- SDJHPPZKZZWAKF-UHFFFAOYSA-N 2,3-dimethylbuta-1,3-diene Chemical compound CC(=C)C(C)=C SDJHPPZKZZWAKF-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 2
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical group [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 2
- 239000003568 Sodium, potassium and calcium salts of fatty acids Substances 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 229910052698 phosphorus Inorganic materials 0.000 description 2
- 239000011574 phosphorus Substances 0.000 description 2
- PMJHHCWVYXUKFD-UHFFFAOYSA-N piperylene Natural products CC=CC=C PMJHHCWVYXUKFD-UHFFFAOYSA-N 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 description 1
- 238000005160 1H NMR spectroscopy Methods 0.000 description 1
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
- OYUNTGBISCIYPW-UHFFFAOYSA-N 2-chloroprop-2-enenitrile Chemical compound ClC(=C)C#N OYUNTGBISCIYPW-UHFFFAOYSA-N 0.000 description 1
- WROUWQQRXUBECT-UHFFFAOYSA-N 2-ethylacrylic acid Chemical compound CCC(=C)C(O)=O WROUWQQRXUBECT-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 238000004566 IR spectroscopy Methods 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 229910021604 Rhodium(III) chloride Inorganic materials 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- LYEZAEXHLSEXON-UHFFFAOYSA-N [RhH3].C1(=CC=CC=C1)P(C1=CC=CC=C1)C1=CC=CC=C1.C1(=CC=CC=C1)P(C1=CC=CC=C1)C1=CC=CC=C1.C1(=CC=CC=C1)P(C1=CC=CC=C1)C1=CC=CC=C1.C1(=CC=CC=C1)P(C1=CC=CC=C1)C1=CC=CC=C1 Chemical compound [RhH3].C1(=CC=CC=C1)P(C1=CC=CC=C1)C1=CC=CC=C1.C1(=CC=CC=C1)P(C1=CC=CC=C1)C1=CC=CC=C1.C1(=CC=CC=C1)P(C1=CC=CC=C1)C1=CC=CC=C1.C1(=CC=CC=C1)P(C1=CC=CC=C1)C1=CC=CC=C1 LYEZAEXHLSEXON-UHFFFAOYSA-N 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 150000001450 anions Chemical group 0.000 description 1
- 229910052785 arsenic Inorganic materials 0.000 description 1
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical group [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 150000004678 hydrides Chemical class 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 239000007764 o/w emulsion Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 235000013966 potassium salts of fatty acid Nutrition 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- FCQRKDSALKMOGU-UHFFFAOYSA-K rhodium(3+);triphenylphosphane;trichloride Chemical compound Cl[Rh](Cl)Cl.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 FCQRKDSALKMOGU-UHFFFAOYSA-K 0.000 description 1
- SONJTKJMTWTJCT-UHFFFAOYSA-K rhodium(iii) chloride Chemical compound [Cl-].[Cl-].[Cl-].[Rh+3] SONJTKJMTWTJCT-UHFFFAOYSA-K 0.000 description 1
- QBERHIJABFXGRZ-UHFFFAOYSA-M rhodium;triphenylphosphane;chloride Chemical compound [Cl-].[Rh].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 QBERHIJABFXGRZ-UHFFFAOYSA-M 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 235000013875 sodium salts of fatty acid Nutrition 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
- 229910052717 sulfur Chemical group 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- 150000007934 α,β-unsaturated carboxylic acids Chemical class 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CA002304501A CA2304501A1 (en) | 2000-04-10 | 2000-04-10 | Process for hydrogenating carboxylated nitrile rubber, the hydrogenated rubber and its uses |
| CA2,304,501 | 2000-04-10 | ||
| PCT/CA2001/000485 WO2001077185A1 (en) | 2000-04-10 | 2001-04-09 | Process for hydrogenating carboxylated nitrile rubber, the hydrogenated rubber and its uses |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2003530467A JP2003530467A (ja) | 2003-10-14 |
| JP2003530467A5 true JP2003530467A5 (enExample) | 2007-04-26 |
| JP4694082B2 JP4694082B2 (ja) | 2011-06-01 |
Family
ID=4165825
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2001575655A Expired - Lifetime JP4694082B2 (ja) | 2000-04-10 | 2001-04-09 | カルボキシル化ニトリルゴムの水素化方法 |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US7265185B2 (enExample) |
| EP (1) | EP1276773B1 (enExample) |
| JP (1) | JP4694082B2 (enExample) |
| KR (1) | KR20030007512A (enExample) |
| CN (1) | CN100523013C (enExample) |
| AT (1) | ATE454406T1 (enExample) |
| AU (1) | AU2001252059A1 (enExample) |
| BR (1) | BR0109933B1 (enExample) |
| CA (1) | CA2304501A1 (enExample) |
| DE (1) | DE60141007D1 (enExample) |
| HU (1) | HUP0300336A3 (enExample) |
| MX (1) | MXPA02009754A (enExample) |
| PL (1) | PL358059A1 (enExample) |
| RU (1) | RU2002129931A (enExample) |
| SK (1) | SK14482002A3 (enExample) |
| WO (1) | WO2001077185A1 (enExample) |
Families Citing this family (51)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE10102047A1 (de) | 2001-01-17 | 2002-07-18 | Bayer Ag | Kautschukmischungen für Walzenbeläge |
| CA2355578A1 (en) | 2001-07-31 | 2003-01-31 | Bayer Inc. | Covulcanisation of polymers |
| US6905319B2 (en) * | 2002-01-29 | 2005-06-14 | Halliburton Energy Services, Inc. | Stator for down hole drilling motor |
| CA2413636A1 (en) * | 2002-12-05 | 2004-06-05 | Bayer Inc. | Adhesive compositions |
| CA2413607A1 (en) * | 2002-12-05 | 2004-06-05 | Bayer Inc. | Process for the preparation of low molecular weight hydrogenated nitrile rubber |
| US20040132886A1 (en) * | 2003-01-06 | 2004-07-08 | Jian Tao | Accelerator free nitrile gloves |
| CA2428222A1 (en) * | 2003-05-08 | 2004-11-08 | Bayer Inc. | Rubber compound comprising nitrile rubbers |
| DE10321875A1 (de) * | 2003-05-15 | 2004-12-02 | Bayer Ag | HXNBR-Kautschuk als Vernetzungsmittel |
| DE10327452A1 (de) * | 2003-06-18 | 2005-01-05 | Bayer Materialscience Ag | Klebstoffe |
| CA2437406A1 (en) * | 2003-08-14 | 2005-02-14 | Bayer Inc. | Butyl compositions comprising nitrile polymers |
| CA2438111A1 (en) * | 2003-08-25 | 2005-02-25 | Bayer Inc. | Nitrile polymer compounds for magntic seal applications |
| CA2452910A1 (en) * | 2003-12-12 | 2005-06-12 | Bayer Inc. | Butyl rubber composition for tire treads |
| CA2452863A1 (en) * | 2003-12-12 | 2005-06-12 | Bayer Inc. | Rubber composition for tire treads |
| CA2478431A1 (en) * | 2004-06-23 | 2005-12-23 | Richard Pazur | Elastomeric compositions having improved mechanical properties and scorch resistance |
| US20060110559A1 (en) * | 2004-10-05 | 2006-05-25 | Victor Nasreddine | Crosslinking of carboxylated nitrile polymers with organo functional silanes: a curable plasticizer composition |
| CA2487744A1 (en) | 2004-11-18 | 2006-05-18 | Lanxess Inc. | Peroxide curable rubber composition comprising hnbr |
| JP4791725B2 (ja) * | 2004-11-19 | 2011-10-12 | 日本板硝子株式会社 | 歯付ベルトを補強するための補強用シートならびに歯付ベルトおよびその製造方法 |
| CA2490046A1 (en) * | 2004-12-10 | 2006-06-10 | Lanxess Inc. | Multistage process for the manufacture of peroxide-cured hxnbr-polyamide thermoplastic vulcanizates |
| CA2501203A1 (en) * | 2005-03-18 | 2006-09-18 | Lanxess Inc. | Hydrogenation of diene-based polymer latex |
| CA2501199A1 (en) * | 2005-03-18 | 2006-09-18 | Lanxess Inc. | Organic solvent-free hydrogenation of diene-based polymers |
| CN100376611C (zh) * | 2005-05-20 | 2008-03-26 | 中国石油天然气股份有限公司 | 一种丁腈橡胶的加氢方法 |
| DE102005042265A1 (de) | 2005-09-06 | 2007-03-08 | Lanxess Deutschland Gmbh | Vernetzbare Zusammensetzungen, daraus erhältliche thermoplastische Elastomere und deren Verwendung |
| DE102005047115A1 (de) | 2005-09-30 | 2007-04-05 | Lanxess Deutschland Gmbh | Vernetzbare Zusammensetzungen, Verfahren zu deren Herstellung und deren Verwendung |
| US7741392B2 (en) * | 2006-02-23 | 2010-06-22 | Lanxess Inc. | Rubber compositions having improved physical and low temperature properties |
| US7666950B2 (en) * | 2006-06-01 | 2010-02-23 | Lanxess Deutschland Gmbh | Process for preparing hydrogenated nitrile rubbers |
| JP4669443B2 (ja) * | 2006-06-12 | 2011-04-13 | 三菱電線工業株式会社 | シール材用ゴム組成物およびそれを用いたシール材 |
| US7765720B2 (en) | 2007-01-12 | 2010-08-03 | Nike, Inc, | Outsole for an article of footwear |
| FR2919613B1 (fr) | 2007-07-30 | 2009-10-09 | Inergy Automotive Systems Res | Objet a base d'une composition contenant un melange reticule d'elastomeres |
| US7858540B2 (en) * | 2007-12-21 | 2010-12-28 | Honeywell International Inc. | Environmentally resistant ballistic composite based on a nitrile rubber binder |
| JP4792053B2 (ja) * | 2008-03-19 | 2011-10-12 | 日本板硝子株式会社 | 補強用繊維に塗布される水性処理剤 |
| BRPI0806233A2 (pt) | 2008-06-23 | 2011-09-06 | Lanxess Deutschland Gmbh | composição vulcanizável, processo de preparação da composição vulcanizável, método de preparação de polìmero vulcanizado e polìmero vulcanizado |
| PL2368916T3 (pl) * | 2010-03-25 | 2013-03-29 | Lanxess Int Sa | Sposób wytwarzania kauczuków nitrylowych wolnych od wody i rozpuszczalników |
| CN101870744A (zh) * | 2010-06-11 | 2010-10-27 | 北京化工大学 | 一种丁腈酯橡胶的加氢方法 |
| US8091855B1 (en) * | 2010-06-30 | 2012-01-10 | Hydril Usa Manufacturing Llc | Fluorinated elastomeric blowout preventer packers and method |
| CN101987874A (zh) * | 2010-09-15 | 2011-03-23 | 郴州高鑫铂业有限公司 | 一种纳米Pd/C催化剂合成氢化丁腈橡胶的方法 |
| BR112013024969A2 (pt) | 2011-03-31 | 2016-12-20 | Zeon Corp | composição de borracha de nitrila, e, método de produção da composição de borracha de nitrila |
| US9484123B2 (en) | 2011-09-16 | 2016-11-01 | Prc-Desoto International, Inc. | Conductive sealant compositions |
| CN102875861A (zh) * | 2012-10-17 | 2013-01-16 | 浙江固特气动机械有限公司 | 用于火电除灰阀门密封圈的改性氢化丁腈材料及其制造工艺 |
| EP2868676A1 (de) | 2013-10-30 | 2015-05-06 | LANXESS Deutschland GmbH | Funktionalisierter nitrilgruppenhaltiger Copolymerkautschuk |
| EP2918612B1 (de) | 2014-03-10 | 2016-09-07 | ARLANXEO Deutschland GmbH | Aminomethylgruppenhaltiger hydrierter nitrilkautschuk, verfahren zu dessen herstellung, vulkanisierbare zusammensetzungen enthaltend aminomethylgruppenhaltigen hydrierten nitrilkautschuk, verfahren zu deren vulkanisation und dadurch erhältliche vulkanisate |
| EP3196239A1 (de) | 2016-01-25 | 2017-07-26 | ARLANXEO Deutschland GmbH | Vulkanisierbare zusammensetzungen auf basis von hydriertem nitrilkautschuk, verfahren zu deren herstellung und deren verwendung |
| EP3248989B1 (en) * | 2016-05-23 | 2020-12-02 | University Of Waterloo | Hydrogenation of nitrile groups in hydrogenated nitrile butadiene rubber and tandem hydrogenation of nitrile groups and olefinic groups in nitrile butadiene rubber using a ruthenium or rhodium complex and a basic reagent |
| EP3248988B1 (en) * | 2016-05-23 | 2020-12-02 | University Of Waterloo | Hydrogenation of nitrile groups in hydrogenated nitrile butadiene rubber and tandem hydrogenation of nitrile groups and olefinic groups in nitrile butadiene rubber using an unsupported rhodium containing catalyst |
| EP3255088B1 (de) | 2016-06-07 | 2020-04-29 | ARLANXEO Deutschland GmbH | Verwendung von vulkanisierbaren zusammensetzungen und vulkanisaten in kontakt mit kühlmittel enthaltend silan-beschichteten wollastonit |
| EP3668922B1 (de) | 2017-08-16 | 2022-03-16 | ARLANXEO Deutschland GmbH | Vulkanisierbare zusammensetzungen enthaltend hydrierten nitrilkautschuk, daraus hergestellte vulkanisate und deren verwendung |
| JP7252212B2 (ja) | 2017-09-20 | 2023-04-04 | アランセオ・ドイチュランド・ゲーエムベーハー | 高い熱伝導性を有する加硫可能なｈｎｂｒ組成物 |
| US11370849B2 (en) * | 2018-01-26 | 2022-06-28 | Zeon Corporation | Method for producing carboxy group-containing hydrogenated nitrile rubber |
| EP3770309B1 (en) * | 2018-03-19 | 2023-08-09 | Nippon Sheet Glass Company, Limited | Cord for rubber reinforcement, method for producing same, and rubber product |
| CN108993608B (zh) * | 2018-07-27 | 2020-11-06 | 北京化工大学 | 一种多功能催化剂及产氢加氢合成氢化丁腈橡胶的方法 |
| CN112940185B (zh) * | 2021-03-29 | 2022-04-22 | 黄河三角洲京博化工研究院有限公司 | 一种共聚物胶乳的选择性加氢方法 |
| WO2025219242A1 (en) | 2024-04-18 | 2025-10-23 | ARLANXEO High Performance Elastomers (Changzhou) Co., Ltd. | Binder composition for an electrochemical energy storage device and method of preparing the same |
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| DE2539132C2 (de) * | 1975-09-03 | 1987-04-09 | Bayer Ag, 5090 Leverkusen | Verwendung hydrierter Dien-Copolymere als temperaturbeständige Materialien auf dem Dichtungssektor |
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| DE3329974A1 (de) | 1983-08-19 | 1985-02-28 | Bayer Ag, 5090 Leverkusen | Herstellung von hydrierten nitrilkautschuken |
| DE3433392A1 (de) | 1984-09-12 | 1986-03-20 | Bayer Ag, 5090 Leverkusen | Hydrierung nitrilgruppenhaltiger ungesaettigter polymerer |
| DE3618907A1 (de) * | 1986-06-05 | 1987-12-10 | Bayer Ag | Verbundwerkstoffe aus vorbehandeltem fasermaterial und vulkanisaten aus hnbr |
| JPH0796629B2 (ja) | 1987-06-29 | 1995-10-18 | 日本ゼオン株式会社 | ゴム組成物 |
| US4843114A (en) * | 1988-01-29 | 1989-06-27 | The United States Of America As Represented By The Secretary Of The Army | Rubber compound for tracked vehicle track pads |
| US4914160A (en) * | 1988-06-23 | 1990-04-03 | Hormoz Azizian | Deuteration of unsaturated polymers and copolymers |
| JPH03220206A (ja) * | 1989-10-26 | 1991-09-27 | Asahi Chem Ind Co Ltd | テレケリック液状水素化ニトリルゴムおよびその製造方法 |
| CN1058218C (zh) * | 1993-06-09 | 2000-11-08 | 机械工厂股份有限公司 | 用注塑法制造的部分结晶合成树脂预塑坯料的加热方法和装置 |
| US5852093A (en) * | 1994-11-30 | 1998-12-22 | Nippon Zeon Co., Ltd. | Vulcanizable rubber composition, seal used in dynamic state, and sealing material |
| US5561197A (en) * | 1995-06-27 | 1996-10-01 | University Of Waterloo | Hydrogenation of diene copolymers |
| CN1058725C (zh) * | 1997-05-08 | 2000-11-22 | 南帝化学工业股份有限公司 | 一种不饱和共聚物加氢的方法及其所用的含双金属的催化剂体系 |
| DE19753302A1 (de) * | 1997-12-01 | 1999-06-02 | Basf Ag | Verfahren zur selektiven Hydrierung von ethylenisch ungesättigten Doppelbindungen in Polymerisaten |
-
2000
- 2000-04-10 CA CA002304501A patent/CA2304501A1/en not_active Withdrawn
-
2001
- 2001-04-09 PL PL01358059A patent/PL358059A1/xx not_active Application Discontinuation
- 2001-04-09 AU AU2001252059A patent/AU2001252059A1/en not_active Abandoned
- 2001-04-09 MX MXPA02009754A patent/MXPA02009754A/es active IP Right Grant
- 2001-04-09 WO PCT/CA2001/000485 patent/WO2001077185A1/en not_active Ceased
- 2001-04-09 US US10/258,245 patent/US7265185B2/en not_active Expired - Lifetime
- 2001-04-09 BR BRPI0109933-7A patent/BR0109933B1/pt not_active IP Right Cessation
- 2001-04-09 DE DE60141007T patent/DE60141007D1/de not_active Expired - Lifetime
- 2001-04-09 SK SK1448-2002A patent/SK14482002A3/sk not_active Application Discontinuation
- 2001-04-09 EP EP01925236A patent/EP1276773B1/en not_active Expired - Lifetime
- 2001-04-09 KR KR1020027013519A patent/KR20030007512A/ko not_active Abandoned
- 2001-04-09 CN CNB018078958A patent/CN100523013C/zh not_active Expired - Lifetime
- 2001-04-09 JP JP2001575655A patent/JP4694082B2/ja not_active Expired - Lifetime
- 2001-04-09 HU HU0300336A patent/HUP0300336A3/hu unknown
- 2001-04-09 RU RU2002129931/04A patent/RU2002129931A/ru not_active Application Discontinuation
- 2001-04-09 AT AT01925236T patent/ATE454406T1/de not_active IP Right Cessation
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