CN111087650A - 一种氟橡胶用硫化剂体系、氟橡胶混炼胶及应用 - Google Patents
一种氟橡胶用硫化剂体系、氟橡胶混炼胶及应用 Download PDFInfo
- Publication number
- CN111087650A CN111087650A CN201911357744.8A CN201911357744A CN111087650A CN 111087650 A CN111087650 A CN 111087650A CN 201911357744 A CN201911357744 A CN 201911357744A CN 111087650 A CN111087650 A CN 111087650A
- Authority
- CN
- China
- Prior art keywords
- parts
- fluororubber
- compound
- hydroxyphenyl
- bisphenol
- 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.)
- Granted
Links
- 229920001973 fluoroelastomer Polymers 0.000 title claims abstract description 70
- 150000001875 compounds Chemical class 0.000 title claims abstract description 37
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 27
- 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 abstract description 26
- USFRYJRPHFMVBZ-UHFFFAOYSA-M benzyl(triphenyl)phosphanium;chloride Chemical compound [Cl-].C=1C=CC=CC=1[P+](C=1C=CC=CC=1)(C=1C=CC=CC=1)CC1=CC=CC=C1 USFRYJRPHFMVBZ-UHFFFAOYSA-M 0.000 claims abstract description 22
- RRRLACFSCYKKIJ-UHFFFAOYSA-N 4-[2,2,2-trifluoro-1,1-bis(4-hydroxyphenyl)ethyl]phenol Chemical compound C1=CC(O)=CC=C1C(C(F)(F)F)(C=1C=CC(O)=CC=1)C1=CC=C(O)C=C1 RRRLACFSCYKKIJ-UHFFFAOYSA-N 0.000 claims abstract description 14
- 239000002994 raw material Substances 0.000 claims abstract description 10
- 235000013824 polyphenols Nutrition 0.000 claims abstract description 9
- 239000002253 acid Substances 0.000 claims abstract description 8
- 239000000945 filler Substances 0.000 claims abstract description 7
- 150000004010 onium ions Chemical class 0.000 claims abstract description 6
- 238000007789 sealing Methods 0.000 claims abstract description 6
- 239000002250 absorbent Substances 0.000 claims abstract description 5
- 230000002745 absorbent Effects 0.000 claims abstract description 5
- 238000004040 coloring Methods 0.000 claims abstract description 5
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims description 16
- 229910052731 fluorine Inorganic materials 0.000 claims description 16
- 239000011737 fluorine Substances 0.000 claims description 16
- -1 polyphenol hydroxy compound Chemical class 0.000 claims description 16
- 238000004132 cross linking Methods 0.000 claims description 12
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 claims description 11
- 239000000920 calcium hydroxide Substances 0.000 claims description 11
- 229910001861 calcium hydroxide Inorganic materials 0.000 claims description 11
- 229920001577 copolymer Polymers 0.000 claims description 10
- 239000006229 carbon black Substances 0.000 claims description 9
- 239000004203 carnauba wax Substances 0.000 claims description 9
- 239000000395 magnesium oxide Substances 0.000 claims description 6
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 claims description 6
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical group [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 claims description 6
- BRPSWMCDEYMRPE-UHFFFAOYSA-N 4-[1,1-bis(4-hydroxyphenyl)ethyl]phenol Chemical compound C=1C=C(O)C=CC=1C(C=1C=CC(O)=CC=1)(C)C1=CC=C(O)C=C1 BRPSWMCDEYMRPE-UHFFFAOYSA-N 0.000 claims description 5
- 238000006243 chemical reaction Methods 0.000 claims description 5
- 239000000203 mixture Substances 0.000 claims description 5
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 claims description 4
- 229920001897 terpolymer Polymers 0.000 claims description 4
- 239000001993 wax Substances 0.000 claims description 4
- 238000003682 fluorination reaction Methods 0.000 claims description 3
- 238000000034 method Methods 0.000 claims description 3
- 239000004698 Polyethylene Substances 0.000 claims description 2
- 229920006172 Tetrafluoroethylene propylene Polymers 0.000 claims description 2
- NRCSJPUCBTUPDG-UHFFFAOYSA-N benzyl-chloro-triphenyl-$l^{5}-phosphane Chemical compound C=1C=CC=CC=1P(C=1C=CC=CC=1)(Cl)(C=1C=CC=CC=1)CC1=CC=CC=C1 NRCSJPUCBTUPDG-UHFFFAOYSA-N 0.000 claims description 2
- WUKWITHWXAAZEY-UHFFFAOYSA-L calcium difluoride Chemical compound [F-].[F-].[Ca+2] WUKWITHWXAAZEY-UHFFFAOYSA-L 0.000 claims description 2
- 229910001634 calcium fluoride Inorganic materials 0.000 claims description 2
- 150000002148 esters Chemical class 0.000 claims description 2
- 125000002573 ethenylidene group Chemical group [*]=C=C([H])[H] 0.000 claims description 2
- 239000000178 monomer Substances 0.000 claims description 2
- 239000012188 paraffin wax Substances 0.000 claims description 2
- 229920000573 polyethylene Polymers 0.000 claims description 2
- 239000002516 radical scavenger Substances 0.000 claims description 2
- 229920006029 tetra-polymer Polymers 0.000 claims description 2
- 229920001971 elastomer Polymers 0.000 abstract description 34
- 239000005060 rubber Substances 0.000 abstract description 33
- 230000006835 compression Effects 0.000 abstract description 9
- 238000007906 compression Methods 0.000 abstract description 9
- 239000000126 substance Substances 0.000 abstract description 8
- 238000004073 vulcanization Methods 0.000 description 41
- 238000002156 mixing Methods 0.000 description 18
- 239000004636 vulcanized rubber Substances 0.000 description 17
- 229930185605 Bisphenol Natural products 0.000 description 8
- CQOZJDNCADWEKH-UHFFFAOYSA-N 2-[3,3-bis(2-hydroxyphenyl)propyl]phenol Chemical compound OC1=CC=CC=C1CCC(C=1C(=CC=CC=1)O)C1=CC=CC=C1O CQOZJDNCADWEKH-UHFFFAOYSA-N 0.000 description 7
- 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 7
- 230000000052 comparative effect Effects 0.000 description 7
- 239000000047 product Substances 0.000 description 6
- 238000001816 cooling Methods 0.000 description 5
- 239000007789 gas Substances 0.000 description 5
- 230000000694 effects Effects 0.000 description 4
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 4
- 239000000347 magnesium hydroxide Substances 0.000 description 4
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 229920002725 thermoplastic elastomer Polymers 0.000 description 4
- 238000007792 addition Methods 0.000 description 3
- 150000004714 phosphonium salts Chemical group 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 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 description 2
- XKZQKPRCPNGNFR-UHFFFAOYSA-N 2-(3-hydroxyphenyl)phenol Chemical class OC1=CC=CC(C=2C(=CC=CC=2)O)=C1 XKZQKPRCPNGNFR-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 125000001153 fluoro group Chemical group F* 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- 238000005160 1H NMR spectroscopy Methods 0.000 description 1
- 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 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000004594 Masterbatch (MB) Substances 0.000 description 1
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 239000012267 brine Substances 0.000 description 1
- 239000002041 carbon nanotube Substances 0.000 description 1
- 229910021393 carbon nanotube Inorganic materials 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- AQYSYJUIMQTRMV-UHFFFAOYSA-N hypofluorous acid Chemical compound FO AQYSYJUIMQTRMV-UHFFFAOYSA-N 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000006082 mold release agent Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 238000010060 peroxide vulcanization Methods 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- KSSNXJHPEFVKHY-UHFFFAOYSA-N phenol;hydrate Chemical group O.OC1=CC=CC=C1 KSSNXJHPEFVKHY-UHFFFAOYSA-N 0.000 description 1
- 229940031826 phenolate Drugs 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000012744 reinforcing agent Substances 0.000 description 1
- 238000013040 rubber vulcanization Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 238000003860 storage Methods 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
- C08K5/04—Oxygen-containing compounds
- C08K5/13—Phenols; Phenolates
- C08K5/136—Phenols containing halogens
-
- 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
- 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
- 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
- C08L27/18—Homopolymers or copolymers or tetrafluoroethene
-
- 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
- C08K2003/2206—Oxides; Hydroxides of metals of calcium, strontium or barium
-
- 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
- C08K2003/2217—Oxides; Hydroxides of metals of magnesium
- C08K2003/222—Magnesia, i.e. magnesium oxide
-
- 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
- C08K2201/00—Specific properties of additives
- C08K2201/014—Additives containing two or more different additives of the same subgroup in C08K
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2201/00—Properties
- C08L2201/08—Stabilised against heat, light or radiation or oxydation
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)
Abstract
Description
Claims (9)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201911357744.8A CN111087650B (zh) | 2019-12-25 | 2019-12-25 | 一种氟橡胶用硫化剂体系、氟橡胶混炼胶及应用 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201911357744.8A CN111087650B (zh) | 2019-12-25 | 2019-12-25 | 一种氟橡胶用硫化剂体系、氟橡胶混炼胶及应用 |
Publications (2)
Publication Number | Publication Date |
---|---|
CN111087650A true CN111087650A (zh) | 2020-05-01 |
CN111087650B CN111087650B (zh) | 2021-06-29 |
Family
ID=70397262
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201911357744.8A Active CN111087650B (zh) | 2019-12-25 | 2019-12-25 | 一种氟橡胶用硫化剂体系、氟橡胶混炼胶及应用 |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN111087650B (zh) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN114262441A (zh) * | 2021-12-16 | 2022-04-01 | 浙江加诚新材料股份有限公司 | 一种含氟苯基硅氧烷侧链的双酚化合物、氟橡胶用硫化剂体系和氟硅橡胶 |
CN115216250A (zh) * | 2022-01-06 | 2022-10-21 | 广东硕成科技股份有限公司 | 一种高稳定性涂布胶及其制备方法 |
CN115584141A (zh) * | 2022-10-27 | 2023-01-10 | 四川道弘新材料有限公司 | 一种耐锂电池电解液双酚高氟氟橡胶混炼胶及其制备方法 |
Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2003040206A1 (fr) * | 2001-11-07 | 2003-05-15 | Toray Industries, Inc. | Compositions de resine epoxy pour materiaux composites a fibres, procede de production de ces materiaux, et materiaux composites a fibres |
US20030208003A1 (en) * | 2002-05-02 | 2003-11-06 | Schmiegel Walter Werner | Curable base-resistant fluoroelastomers |
CN1745112A (zh) * | 2003-01-29 | 2006-03-08 | 特拉华特威德·格林公司 | 用于全氟弹性体组合物的基于双氨基苯基的固化剂和基于脒的固化剂以及固化促进剂 |
CN101153120A (zh) * | 2007-08-28 | 2008-04-02 | 扬中市橡胶塑料厂 | 一种改性的氟橡胶混炼胶及其制备方法 |
CN101362700A (zh) * | 2008-09-08 | 2009-02-11 | 中国科学院化学研究所 | 双邻羟基含氟芳香族二胺化合物及其制备方法与应用 |
CN104327426A (zh) * | 2014-10-24 | 2015-02-04 | 海宁市加诚橡胶有限公司 | 可与硅橡胶粘接的氟橡胶配方 |
CN106752442A (zh) * | 2016-12-09 | 2017-05-31 | 南阳天密封股份有限公司 | 一种氟橡胶金属复合板及其制备方法 |
CN109535613A (zh) * | 2017-09-21 | 2019-03-29 | 中昊晨光化工研究院有限公司 | 一种氟橡胶混炼胶及其制备方法 |
-
2019
- 2019-12-25 CN CN201911357744.8A patent/CN111087650B/zh active Active
Patent Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2003040206A1 (fr) * | 2001-11-07 | 2003-05-15 | Toray Industries, Inc. | Compositions de resine epoxy pour materiaux composites a fibres, procede de production de ces materiaux, et materiaux composites a fibres |
US20030208003A1 (en) * | 2002-05-02 | 2003-11-06 | Schmiegel Walter Werner | Curable base-resistant fluoroelastomers |
CN1745112A (zh) * | 2003-01-29 | 2006-03-08 | 特拉华特威德·格林公司 | 用于全氟弹性体组合物的基于双氨基苯基的固化剂和基于脒的固化剂以及固化促进剂 |
CN101153120A (zh) * | 2007-08-28 | 2008-04-02 | 扬中市橡胶塑料厂 | 一种改性的氟橡胶混炼胶及其制备方法 |
CN101362700A (zh) * | 2008-09-08 | 2009-02-11 | 中国科学院化学研究所 | 双邻羟基含氟芳香族二胺化合物及其制备方法与应用 |
CN104327426A (zh) * | 2014-10-24 | 2015-02-04 | 海宁市加诚橡胶有限公司 | 可与硅橡胶粘接的氟橡胶配方 |
CN106752442A (zh) * | 2016-12-09 | 2017-05-31 | 南阳天密封股份有限公司 | 一种氟橡胶金属复合板及其制备方法 |
CN109535613A (zh) * | 2017-09-21 | 2019-03-29 | 中昊晨光化工研究院有限公司 | 一种氟橡胶混炼胶及其制备方法 |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN114262441A (zh) * | 2021-12-16 | 2022-04-01 | 浙江加诚新材料股份有限公司 | 一种含氟苯基硅氧烷侧链的双酚化合物、氟橡胶用硫化剂体系和氟硅橡胶 |
CN115216250A (zh) * | 2022-01-06 | 2022-10-21 | 广东硕成科技股份有限公司 | 一种高稳定性涂布胶及其制备方法 |
CN115584141A (zh) * | 2022-10-27 | 2023-01-10 | 四川道弘新材料有限公司 | 一种耐锂电池电解液双酚高氟氟橡胶混炼胶及其制备方法 |
CN115584141B (zh) * | 2022-10-27 | 2023-07-18 | 四川道弘新材料有限公司 | 一种耐锂电池电解液双酚高氟氟橡胶混炼胶及其制备方法 |
Also Published As
Publication number | Publication date |
---|---|
CN111087650B (zh) | 2021-06-29 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN111087650B (zh) | 一种氟橡胶用硫化剂体系、氟橡胶混炼胶及应用 | |
US4942202A (en) | Rubber composition and vulcanized rubber product | |
JP5162818B2 (ja) | 含フッ素共重合体ブレンド物 | |
DE69124695T2 (de) | Innenbelagzusammensetzung eines reifens | |
US5053450A (en) | Elastomer compositions | |
JPH073101A (ja) | フルオロエラストマー組成物 | |
US5962589A (en) | Rubber compositions of low compression set | |
WO2005123786A1 (en) | Grafted fluoroelastomers | |
JP4491547B2 (ja) | 含フッ素エラストマー組成物 | |
CN108610562B (zh) | 一种低压变耐高温乙丙橡胶材料及其制备方法 | |
JP2000510499A (ja) | 有機オニウム化合物を含有するフルオロエラストマー組成物 | |
DE69123849T2 (de) | Mischung für reifenseitenwand | |
WO1994022930A1 (en) | Process for producing fluoroelastomer | |
CN112708205B (zh) | 一种低气味抗冲耐划伤聚丙烯组合物及其制备方法 | |
US4433107A (en) | Polyisoprene rubber compositions | |
JP4785713B2 (ja) | 含フッ素エラストマーおよびその組成物 | |
SU1165237A3 (ru) | Резинова смесь на основе этиленового сополимера | |
JPH1044258A (ja) | ゴム物品の製造方法 | |
JPH03100039A (ja) | フルオロエラストマー組成物 | |
US5089563A (en) | High vinyl polybutadiene rubber containing halogen having enhanced cure characteristics | |
JPS58152030A (ja) | ゴム組成物 | |
JPH04501433A (ja) | 結晶性ポリオレフィン樹脂及びハロブチルゴム物質の動的加硫アロイ | |
CN115850886B (zh) | 一种高性能氟橡胶混炼胶及其应用 | |
CA1339237C (en) | High vinyl polybutadiene rubber having enhanced cure characteristics | |
CN113185794A (zh) | 高强度耐磨雨鞋用材料及其制备方法 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
GR01 | Patent grant | ||
GR01 | Patent grant | ||
CP01 | Change in the name or title of a patent holder |
Address after: 314415 Building 1, No.64 Anjiang Road, Jianshan New District, Haining City, Jiaxing City, Zhejiang Province Patentee after: Zhejiang Jiacheng New Material Co.,Ltd. Address before: 314415 Building 1, No.64 Anjiang Road, Jianshan New District, Haining City, Jiaxing City, Zhejiang Province Patentee before: Zhejiang Jiacheng New Materials Co.,Ltd. |
|
CP01 | Change in the name or title of a patent holder | ||
PE01 | Entry into force of the registration of the contract for pledge of patent right |
Denomination of invention: A vulcanizing agent system for fluororubber, fluororubber blend and its application Effective date of registration: 20231222 Granted publication date: 20210629 Pledgee: Huangwan sub branch of Zhejiang Haining Rural Commercial Bank Co.,Ltd. Pledgor: Zhejiang Jiacheng New Material Co.,Ltd. Registration number: Y2023980072891 |
|
PE01 | Entry into force of the registration of the contract for pledge of patent right |