DE2856526C2 - Elastomermasse - Google Patents
ElastomermasseInfo
- Publication number
- DE2856526C2 DE2856526C2 DE2856526A DE2856526A DE2856526C2 DE 2856526 C2 DE2856526 C2 DE 2856526C2 DE 2856526 A DE2856526 A DE 2856526A DE 2856526 A DE2856526 A DE 2856526A DE 2856526 C2 DE2856526 C2 DE 2856526C2
- Authority
- DE
- Germany
- Prior art keywords
- epichlorohydrin
- elastomer
- composition according
- elastomer composition
- hydroxyphenyl
- 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
Links
- 229920001971 elastomer Polymers 0.000 title claims description 22
- 239000000806 elastomer Substances 0.000 title claims description 21
- 239000000203 mixture Substances 0.000 claims description 26
- 229920001973 fluoroelastomer Polymers 0.000 claims description 12
- 238000004073 vulcanization Methods 0.000 claims description 10
- 229920001577 copolymer Polymers 0.000 claims description 9
- 229920005558 epichlorohydrin rubber Polymers 0.000 claims description 9
- 150000001875 compounds Chemical class 0.000 claims description 8
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims description 7
- ZFVMWEVVKGLCIJ-UHFFFAOYSA-N bisphenol AF Chemical compound C1=CC(O)=CC=C1C(C(F)(F)F)(C(F)(F)F)C1=CC=C(O)C=C1 ZFVMWEVVKGLCIJ-UHFFFAOYSA-N 0.000 claims description 7
- 229910052731 fluorine Inorganic materials 0.000 claims description 7
- 239000011737 fluorine Substances 0.000 claims description 7
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 claims description 6
- 239000000370 acceptor Substances 0.000 claims description 5
- 239000002253 acid Substances 0.000 claims description 5
- 238000004132 cross linking Methods 0.000 claims description 3
- 239000003431 cross linking reagent Substances 0.000 claims description 3
- 239000000178 monomer Substances 0.000 claims description 3
- 229920000642 polymer Polymers 0.000 claims description 3
- XBQISEWBYMWLET-UHFFFAOYSA-N 4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)phenol Chemical compound OC1=CC=C(C(O)(C(F)(F)F)C(F)(F)F)C=C1 XBQISEWBYMWLET-UHFFFAOYSA-N 0.000 claims description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 2
- 239000000654 additive Substances 0.000 claims description 2
- 229910052783 alkali metal Inorganic materials 0.000 claims description 2
- 150000001340 alkali metals Chemical class 0.000 claims description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims description 2
- -1 alkaline earth metal salt Chemical class 0.000 claims description 2
- 229920001519 homopolymer Polymers 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 10
- BQCIDUSAKPWEOX-UHFFFAOYSA-N 1,1-Difluoroethene Chemical compound FC(F)=C BQCIDUSAKPWEOX-UHFFFAOYSA-N 0.000 description 6
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 6
- 125000000217 alkyl group Chemical group 0.000 description 5
- 239000002585 base Substances 0.000 description 4
- 230000000704 physical effect Effects 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- IMNIMPAHZVJRPE-UHFFFAOYSA-N triethylenediamine Chemical compound C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 description 4
- 239000006229 carbon black Substances 0.000 description 3
- 229920005562 epichlorohydrin/ethylene oxide copolymer Polymers 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 230000003064 anti-oxidating effect Effects 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 2
- 239000000920 calcium hydroxide Substances 0.000 description 2
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- XMFOQHDPRMAJNU-UHFFFAOYSA-N lead(ii,iv) oxide Chemical compound O1[Pb]O[Pb]11O[Pb]O1 XMFOQHDPRMAJNU-UHFFFAOYSA-N 0.000 description 2
- 239000000395 magnesium oxide Substances 0.000 description 2
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 2
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 150000007522 mineralic acids Chemical class 0.000 description 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 2
- 150000007524 organic acids Chemical class 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- NDMMKOCNFSTXRU-UHFFFAOYSA-N 1,1,2,3,3-pentafluoroprop-1-ene Chemical compound FC(F)C(F)=C(F)F NDMMKOCNFSTXRU-UHFFFAOYSA-N 0.000 description 1
- BLTXWCKMNMYXEA-UHFFFAOYSA-N 1,1,2-trifluoro-2-(trifluoromethoxy)ethene Chemical compound FC(F)=C(F)OC(F)(F)F BLTXWCKMNMYXEA-UHFFFAOYSA-N 0.000 description 1
- BZPCMSSQHRAJCC-UHFFFAOYSA-N 1,2,3,3,4,4,5,5,5-nonafluoro-1-(1,2,3,3,4,4,5,5,5-nonafluoropent-1-enoxy)pent-1-ene Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(F)=C(F)OC(F)=C(F)C(F)(F)C(F)(F)C(F)(F)F BZPCMSSQHRAJCC-UHFFFAOYSA-N 0.000 description 1
- YHMYGUUIMTVXNW-UHFFFAOYSA-N 1,3-dihydrobenzimidazole-2-thione Chemical compound C1=CC=C2NC(S)=NC2=C1 YHMYGUUIMTVXNW-UHFFFAOYSA-N 0.000 description 1
- AGPJEGDSGBAREQ-UHFFFAOYSA-N 2-chloro-1,3,3,4,4,5,6,6,7,8,8,8-dodecafluorooct-1-ene Chemical compound FC(C(F)(F)F)C(C(C(C(C(=CF)Cl)(F)F)(F)F)F)(F)F AGPJEGDSGBAREQ-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 229920002313 fluoropolymer Polymers 0.000 description 1
- 239000004811 fluoropolymer Substances 0.000 description 1
- HCDGVLDPFQMKDK-UHFFFAOYSA-N hexafluoropropylene Chemical compound FC(F)=C(F)C(F)(F)F HCDGVLDPFQMKDK-UHFFFAOYSA-N 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000011133 lead Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000006259 organic additive Substances 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 150000003018 phosphorus compounds Chemical class 0.000 description 1
- 239000003566 sealing material Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 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
- C08L27/00—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 a halogen; Compositions of derivatives of such polymers
- C08L27/02—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 a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L27/12—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 a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
- C08L27/16—Homopolymers or copolymers or vinylidene fluoride
-
- 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
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
-
- 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
- C08K5/05—Alcohols; Metal alcoholates
-
- 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
- C08K5/16—Nitrogen-containing compounds
- C08K5/17—Amines; Quaternary ammonium compounds
-
- 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
- C08K5/49—Phosphorus-containing compounds
- C08K5/50—Phosphorus bound to carbon only
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L71/00—Compositions of polyethers obtained by reactions forming an ether link in the main chain; Compositions of derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L71/00—Compositions of polyethers obtained by reactions forming an ether link in the main chain; Compositions of derivatives of such polymers
- C08L71/02—Polyalkylene oxides
- C08L71/03—Polyepihalohydrins
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)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP52160343A JPS5946539B2 (ja) | 1977-12-30 | 1977-12-30 | エラストマ−組成物 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE2856526A1 DE2856526A1 (de) | 1979-07-05 |
| DE2856526C2 true DE2856526C2 (de) | 1987-04-09 |
Family
ID=15712920
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE2856526A Expired DE2856526C2 (de) | 1977-12-30 | 1978-12-28 | Elastomermasse |
Country Status (6)
Families Citing this family (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS608052B2 (ja) * | 1978-10-07 | 1985-02-28 | ダイキン工業株式会社 | 新規フルオロエラストマ−の共架橋用ブレンド組成物 |
| US4343861A (en) | 1979-10-23 | 1982-08-10 | Minnesota Mining And Manufacturing Company | Fluoroelastomer/polyepichlorohydrin elastomer articles |
| US4293663A (en) | 1979-10-23 | 1981-10-06 | Minnesota Mining And Manufacturing Company | Fluoroelastomer/polyepichlorohydrin elastomer articles |
| US4287322A (en) | 1979-10-23 | 1981-09-01 | Minnesota Mining And Manufacturing Company | Epichlorohydrin elastomer compositions |
| BR8008879A (pt) * | 1979-10-23 | 1981-08-25 | Minnesota Mining & Mfg | Composicoes elastoemras de epicloridrina |
| GB2088385A (en) * | 1980-11-21 | 1982-06-09 | Bostik Ltd | Curable fluorocarbon polymer compositions |
| US4358559A (en) | 1981-11-19 | 1982-11-09 | Minnesota Mining And Manufacturing Company | Tacky fluoroelastomer compositions |
| CA1195793A (en) * | 1981-12-28 | 1985-10-22 | Lester T. Toy | Elastomer based adhesive compositions |
| DE3583598D1 (de) * | 1984-12-27 | 1991-08-29 | Asahi Glass Co Ltd | Haertbare harzmischung. |
| IT1188202B (it) * | 1985-11-15 | 1988-01-07 | Ausimont Spa | Composizioni elastomeriche vulcanizzabili di fluoroelastomeri |
| IT1209669B (it) * | 1985-11-15 | 1989-08-30 | Ausimont Spa | Composizioni vulcanizzabili fluoroelastomeri aventi migliorate caratteristiche di processabilita'e di stabilita' chimica. |
| JP2610145B2 (ja) * | 1987-11-20 | 1997-05-14 | 日本合成ゴム株式会社 | ゴム組成物 |
| JP2787073B2 (ja) * | 1989-10-13 | 1998-08-13 | ジェイエスアール株式会社 | ゴム組成物 |
| US5552199A (en) * | 1994-09-02 | 1996-09-03 | Minnesota Mining And Manufacturing Company | Melt-processable electroconductive fluoroplastic |
| US6239223B1 (en) | 1997-09-05 | 2001-05-29 | Chemfab Corporation | Fluoropolymeric composition |
| JP5114826B2 (ja) * | 2005-02-04 | 2013-01-09 | ダイキン工業株式会社 | 架橋性組成物およびそれからなる積層体 |
| US7553894B2 (en) * | 2005-07-28 | 2009-06-30 | 3M Innovative Properties Company | Cold-shrink article and method of making cold-shrink article |
| JP4695950B2 (ja) * | 2005-09-20 | 2011-06-08 | 株式会社エクシム | 常温収縮チューブの製造方法及び常温収縮チューブ |
| US7705085B2 (en) * | 2007-04-06 | 2010-04-27 | 3M Innovative Properties Company | Fluoroelastomer composition for cold shrink articles |
| US7642460B2 (en) * | 2007-04-06 | 2010-01-05 | 3M Innovative Properties Company | Cold shrinkable article including a fluoroelastomer composition |
| US8188178B2 (en) | 2007-05-07 | 2012-05-29 | 3M Innovative Properties Company | Cold shrinkable article including an epichlorohydrin composition |
| US20080280080A1 (en) * | 2007-05-07 | 2008-11-13 | Bandyopadhyay Pradip K | Cold shrinkable article including an epichlorohydrin composition |
| US7973241B2 (en) | 2007-09-10 | 2011-07-05 | 3M Innovative Properties Company | Pressure restraining enclosure for cables |
| US7635813B2 (en) * | 2007-09-10 | 2009-12-22 | 3M Innovative Properties Company | Article and method for sealing fluid-containing cables |
| 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 |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2904528A (en) * | 1954-12-30 | 1959-09-15 | Minnesota Mining & Mfg | Composition comprising epoxide resin and trifluorochloroolefin copolymer and process of crosslinking same |
| US3424818A (en) * | 1965-10-21 | 1969-01-28 | Exxon Research Engineering Co | Cured pvc-rubber and resin blends |
| DE1769987B2 (de) * | 1967-08-17 | 1977-03-31 | E.I. du Pont de Nemours and Co., Wilmington, Del. (V.StA.) | Waermehaertbare massen aus vinylidenfluoridcopolymerisaten |
| US3872065A (en) * | 1973-10-03 | 1975-03-18 | Du Pont | Vulcanizable fluoroelastomer composition |
| US4141874A (en) * | 1975-11-15 | 1979-02-27 | Daikin Kogyo Co., Ltd. | Fluorine-containing elastomeric copolymers, process for preparing the same and composition containing the same |
-
1977
- 1977-12-30 JP JP52160343A patent/JPS5946539B2/ja not_active Expired
-
1978
- 1978-12-20 GB GB7849213A patent/GB2011924B/en not_active Expired
- 1978-12-28 FR FR7836715A patent/FR2413426B1/fr not_active Expired
- 1978-12-28 DE DE2856526A patent/DE2856526C2/de not_active Expired
- 1978-12-29 US US05/974,239 patent/US4188352A/en not_active Expired - Lifetime
- 1978-12-29 IT IT31409/78A patent/IT1121755B/it active
Also Published As
| Publication number | Publication date |
|---|---|
| IT1121755B (it) | 1986-04-23 |
| IT7831409A0 (it) | 1978-12-29 |
| DE2856526A1 (de) | 1979-07-05 |
| GB2011924B (en) | 1982-03-17 |
| GB2011924A (en) | 1979-07-18 |
| JPS5493040A (en) | 1979-07-23 |
| FR2413426B1 (fr) | 1985-11-22 |
| JPS5946539B2 (ja) | 1984-11-13 |
| FR2413426A1 (fr) | 1979-07-27 |
| US4188352A (en) | 1980-02-12 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 8110 | Request for examination paragraph 44 | ||
| D2 | Grant after examination | ||
| 8364 | No opposition during term of opposition | ||
| 8339 | Ceased/non-payment of the annual fee |