CN100455624C - Fluororubber composition and molding articles - Google Patents
Fluororubber composition and molding articles Download PDFInfo
- Publication number
- CN100455624C CN100455624C CNB2006100258625A CN200610025862A CN100455624C CN 100455624 C CN100455624 C CN 100455624C CN B2006100258625 A CNB2006100258625 A CN B2006100258625A CN 200610025862 A CN200610025862 A CN 200610025862A CN 100455624 C CN100455624 C CN 100455624C
- Authority
- CN
- China
- Prior art keywords
- viton
- whisker
- fluoro
- weight part
- rubber composite
- 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 - Fee Related
Links
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
Abstract
The invention discloses a fluororubber rubber composition and moulding product, which comprises the following parts: 100wt% fluororubber, 5-50wt% non-metal whisker and 0. 1-5wt% surface activator. The invention possesses high stretching strength and modulus, which improves heat resistance and abrasion resistance.
Description
Technical field
The present invention relates to fluoro-rubber composite and moulded products thereof, especially for the fluoro-rubber composite and the moulded products thereof of seal applications.
Background technology
Viton is a kind of high temperature resistant, and the rubber of media-resistant is widely used in the manufacturing engine oil seal, goods such as seal gum.But the decay of the conventional physicals of viton is very fast under hot conditions, so the physicals need be with normal temperature the time improves as much as possible.Carbon black at present commonly used, white carbon blacks etc. can use under normal conditions as weighting agent, but under the harsher situation of working conditions, as: the deep-well separation scraper in the oil production, crankshaft for automobile engine oil sealing, problems such as present viton all has compression set big, and work-ing life is short.
Therefore, need stable physical property under a kind of hot conditions, compression set is little and the viton goods of long service life.
Summary of the invention
The objective of the invention is to overcome above-mentioned weak point of the prior art, a kind of new fluoro-rubber composite that has greatly improved tensile strength and modulus is provided and has high heat resistance and the moulded products of high-wearing feature.
Another object of the present invention is greatly to improve the dispersiveness of fluoro-rubber composite by the adding fluorochemical surfactant.
Above-mentioned purpose of the present invention can reach with rubber combination as described below and moulded products thereof.Fluoro-rubber composite of the present invention comprises the tensio-active agent of 100 weight part viton, the nonmetal whisker of 5-50 weight part and 0.1-5 weight part.
The present invention also provides the moulded products that makes with above-mentioned fluoro-rubber composite behind sulfidization molding.
Embodiment
Used viton is through the fluorizated elastomeric polymer among the present invention, comprises known in the past all viton.Representational viton can be enumerated as follows: (vinylidene: the R 1216 mol ratio=45-95: 55-5) preferably of vinylidene/R 1216 system, (vinylidene/tetrafluoroethylene/hexafluoropropylene mol ratio=45-90: the 1-35: 5-50) preferably of vinylidene/tetrafluoroethylene/hexafluoropropylene system, vinylidene/trifluorochloroethylene system, tetrafluoroethylene/propylene system, hexafluoropropylene/ethylene system, perfluoroalkyl vinyl ether (comprise and contain a plurality of ehter bond persons)/alkene (tetrafluoroethylene, ethene etc.) be, fluorosilicone system, viton such as fluorine phosphine piperazine system.The viton of forming by vinylidene fluoride monomers and at least a other monomeric multipolymer preferably, is the content of vinylidene fluoride monomers?～80% (weight).In order to improve vulcanization reaction, viton can also be on its polymer chain bonding iodine atom or bromine atoms.The molecular weight of viton (measuring with the gel infiltration method) is 3,000-1, and 200,000 are advisable.
Used nonmetal whisker is meant a kind of whiskers body pottery whisker that grows into the monocrystalline form among the present invention under the manual control condition.This pottery whisker comprises carborundum whisker, silicon nitride crystal whisker, mullite crystal whisker, potassium titanate crystal whisker, aluminium borate whisker, ZnOw, magnesia crystal whisker, calcium sulfate crystal whiskers, calcium carbonate crystal whisker and magnesium salt whisker etc.Preferred pottery whisker comprises potassium titanate crystal whisker, calcium sulfate crystal whiskers, calcium carbonate crystal whisker etc., most preferably potassium titanate crystal whisker.The diameter of pottery whisker is generally several between several microns at zero point, and length is several microns extremely hundreds of microns, preferably controls diameter at the 0.2-2 micron, and length is at the 10-50 micron, and length-to-diameter ratio is advisable at 15-60.
Use the pottery whisker in the fluoro-rubber composite of the present invention, obtained beyond thought effect.In viton, add a certain amount of pottery whisker, the viton goods that can make gained under hot conditions stable physical property, compression set is little and long service life.In addition, tensile strength, modulus and the wear resistance of viton goods can have been improved widely.
With respect to the viton of 100 weight parts, the consumption of nonmetal whisker is preferably the 5-50 weight part, preferably the 10-30 weight part.If 5 parts of the usefulness quantity not sufficients of whisker, the effect performance of whisker is not obvious.When if the consumption of whisker surpasses 50 weight parts, usually cause that physicals reduces, thereby inadvisable.
In order to guarantee whisker uniform distribution in the viton matrix, disordered orientation makes the joint interface of whisker and rubber that bonding closely be arranged firmly, should add a spot of tensio-active agent in fluoro-rubber composite of the present invention.
This tensio-active agent can be a tensio-active agent commonly used in this area, as cats product, anion surfactant, neutral surface active agent or amphoterics commonly used in this area.Yet the preferred fluorochemical surfactant that adds in the fluoro-rubber composite of the present invention is with the consistency of raising with viton.Suitable fluorine surfactant is a United States Patent (USP) 2,732, and those tensio-active agents described in 398 can be exemplified below:
C
4F
9SO
2N(CH
3)H
C
8F
17SO
2N(CH
3)H
C
8F
17SO
2N(CH
3)Na
+
C
8F
17SO
2N(C
12H
25)H
C
8F
17SO
2N(C
6H
5)H
With respect to the viton of 100 weight parts, the consumption of tensio-active agent is the 0.1-5 weight part, preferably the 1-2 weight part.When surpassing 5 weight parts, usually cause the reduction of viton goods physicals, thus inadvisable.
Except said components, can also add various additives commonly used in the viton goods in the fluoro-rubber composite of the present invention, as weighting agent, vulcanizing agent, tinting material, fire retardant, stablizer, softening agent, oil-proof composition, scorch retarder etc.
Above-mentioned weighting agent can be a weighting agent commonly used in the viton field, for example can use magnesium oxide, calcium oxide, ferric oxide, silicon oxide, zinc oxide, plumbous oxide, metal oxides such as aluminum oxide, magnesium hydroxide, aluminium hydroxide, calcium hydroxide, zinc hydroxide, metal hydroxidess such as lead hydroxide, magnesiumcarbonate, aluminium carbonate, broken sour calcium, carbonate such as barium carbonate, Magnesium Silicate q-agent, Calucium Silicate powder, water glass, silicate such as pure aluminium silicate, Tai-Ace S 150, calcium sulfate, vitriol such as barium sulfate, molybdenumdisulphide, iron sulphide, metallic sulfides such as cupric sulfide, silicon bath soil, asbestos, lithopone (zinc sulphide/barium sulfate), graphite, carbon black, fluorocarbons, Calcium Fluoride (Fluorspan), coke, wollastonite, mica powder, glass powder, carbon fibre, quartz powder etc.These weighting agents also can more than 2 kinds and be used.With respect to the viton of 100 weight parts, the amount of weighting agent is the 0-100 weight part, normally the 0-50 weight part.
The vulcanization process of fluoro-rubber composite of the present invention comprises the peroxide cure method of organo-peroxide as vulcanizing agent of using, and uses the polyvalent alcohol sulfuration method of polyol as vulcanizing agent, uses the polyamines sulfuration method of polyamine compounds as vulcanizing agent.Any vulcanization process is all applicable among the present invention, and but, preferable methods is to use the polyvalent alcohol sulfuration method of polyol.With respect to the viton of 100 weight parts, the consumption of vulcanizing agent generally is the 0.05-10 weight part, and preferred consumption is the 0.5-5 weight part.
As organo-peroxide; preferably adopt in the presence of heat or redox system and be easy to generate peroxide-based compound; for example 1; two (tert-butyl hydroperoxide)-3 of 1-; 5; the 5-trimethyl-cyclohexane; 2; 5-dimethylhexane-2; 5 dihydroxyl superoxide; two-tert-butyl peroxide; tertiary butyl cumyl peroxide; dicumyl peroxide; α; α-two (tert-butyl hydroperoxide)-right-diisopropyl benzene; 2; 5-dimethyl-2,5-two (tert-butyl hydroperoxide) hexane; 2,5-dimethyl-2; 5-two (butyl peroxyization) hexane-3; benzoyl peroxide; tert-butyl hydroperoxide benzene; 2; 5-dimethyl-2,5-two (benzoyl peroxidation) hexane; the tert-butyl hydroperoxide toxilic acid; tert-butyl hydroperoxide sec.-propyl carbonic ether etc. wherein, the compound of dioxane base class preferably.Usually, can wait kind and the consumption of selecting compound according to amount, the decomposition temperature of activity-O-O.
In addition, when using organo-peroxide, if suitably and with crosslinking coagent or co-crosslinker, effect is more remarkable.Say that in principle these crosslinking coagents or co-crosslinker have no particular limits its kind as long as having reactive behavior for peroxide-based and monatomic group just can tell on.Preferred crosslinking coagent or co-crosslinker can be enumerated: triallyl cyanurate, cyamelide triallyl, triacryl methylal, trimellitic acid triallyl, N, N '-meta-phenylene bismaleimide, dipropargyl terephthalate, Phthalic acid, diallyl ester, tetraallyl terephthalate and polydimethyl vinylsiloxane, polyphenylmethyl base vinylsiloxane etc. contains the siloxane oligomer of vinyl.With respect to the viton of 100 weight parts, its usage quantity is the 0.1-10 weight part, preferably the 0.5-5 weight part.In addition, but polymkeric substance as the blend co-crosslinking, can also use silicone oil, silicon rubber, ethylene/vinyl acetate multipolymer, 1,2-polyhutadiene, fluorosilicon oil, trifluoropropyl siloxane, fluorine phosphine piperazine rubber, hexafluoropropylene/ethylene multipolymer, tetrafluoroethylene/propylene copolymer, epichloro hydrin rubber (comprising multipolymer) polyurethane rubber, halogenated butyl rubber, butyronitrile rubber etc. can be used the polymkeric substance of peroxide crosslinking.Its usage quantity has no particular limits, but should not increase to the degree of obvious damage polymer property.
As polyol, can use polyol or by chemical formula R with phenolic hydroxyl
f(CH
2OH)
2(R in the formula
fBe polyfluoro alkylidene group or the perchloro-fluorine alkylidene group of carbonatoms 1-20) expression dihydroxy compound or an alkali metal salt of these compounds or their mixture.
The preferred example of these compounds can be enumerated: Resorcinol, 2, two (4-hydroxyphenyl) propane, 2 of 2-, two (4-hydroxyphenyl) perfluoropropane, 2 of 2-, two (4-hydroxyphenyl) butane, 1 of 2-, two (4-hydroxyphenyl) methane, 4 of 1-, 4-dihydroxyphenyl phenyl ether, HOCH
2(CF
2)
2CH
2An alkali metal salt of OH or these compounds etc.
As polyamine compounds, use the uncle's glue or the secondary amine of 2 above basic nitrogens of bonding in the molecule, be to use gentle appropriateness after they are changed salify as a rule so that their reactivity becomes.The object lesson of these compounds, it generally is the Alkylenediamine class, wherein relatively commonly used have ethylenediamine carbamate, hexamethylene-diamine carboxylamine vinegar, 4,4 '-diamines cyclohexyl-methane carbamate etc., in addition, N in addition commonly used, a N ' dicinnamylidene-1, Schiff's base such as 6-hexamethylene-diamine.In addition, the many glue aromatics that lacks alkalescence also can and be used with other basic cpd.Described other basic cpd for example can be a vulkacit D, and diphenyl thiourea etc. also have the promotor and the intramolecularly of use for synthetic rubber to have-NH in addition
2And/or-compound of NE-.The metal hydroxides that also has divalence in addition.
In addition, as required, can also use tertiary amine, three to replace to narrow, the organic acid salt of penta-substituted guanidines or these compounds or inorganic acid salt, quaternary amine, season phosphonium salt or nitrogenous cyclic polyether as crosslinking accelerator.
The blending means of mentioned component can adopt common open roller.In addition, the sulfuration of fluoro-rubber composite of the present invention can be carried out under common vulcanizable fluororubber condition, and it is mixing for example fluoro-rubber composite to be carried out roller, in the metal die of packing into then, and at 150-200 ℃, 3-100kg/cm
2(3-30kg/cm normally
2) kept 3-60 minute under the condition, carry out press vulcanization, in 180-260 ℃ baking oven, keep then carrying out post vulcanization in 0-24 hour, after above-mentioned sulfuration, obtain moulded products.
Moulded products of the present invention can be used for trolley part, separation scrapers such as O RunddichtringO, packing ring, oil sealing, general industry parts etc.
Below by embodiment the present invention is described, but self-evident, the present invention is not subjected to the restriction of these embodiment.
Embodiment
Be listed below the abbreviation of used various raw materials among the embodiment below:
FE2603: vinylidene (VDF)/R 1216 (HFP) multipolymer (mooney viscosity
ML1+10,121 ℃=70), like that available from Shanghai three rich novel material share is limited
Company.
ML11: vinylidene (VDF)/R 1216 (HFP) multipolymer (mooney viscosity
ML1+10,121 ℃=30), available from Meilan Chemical Co., Ltd., Jiangsu
BF6: polyvalent alcohol is the vulcanizing agent bisphenol AF, available from Honeywell Co.
BPP: the vulcanization accelerator quaternary alkylphosphonium salt, available from Rohmhass.
N-990: thermals, available from Cancarb Co
MgO: magnesium oxide, consonance 150
Ca (OH)
2: calcium hydroxide, Lay mattress chemistry CF
BaSO
4: barium sulfate, the two chemical industry that reach in Shanghai
Tismo D: the trade(brand)name of potassium titanate crystal whisker.Mean diameter is 0.3～0.6 μ m, and is average long
Degree is between 10～20 μ m, available from Otsuka Kagaku K.K..
Tensio-active agent: the hot sulphonamide of N-ethyl-N hydroxyethyl perfluor, available from Wuhan De Heng company.
The performance of the fluoro-rubber composite that makes among the following embodiment is tested as follows:
The mensuration of GB1232-1992 unvulcanized rubber mooney viscosity.
GB/T2941-1991 rubbery sample environment is regulated and touchstone temperature, humidity and time.
The test of GB/T528-1996 vulcanized rubber tensile property.
GB/T531-1996 rubber Shao Shi A type hardness tester test method.
The cooperation of GB6038 rubber test sizing material, mixing, sulfuration, equipment and schedule of operation.
The general provision that the test of GB/T5723-1993 hard rubber is measured with test piece and product size.
HG/T2198-1991 vulcanized rubber physical test method general requirement.
Embodiment 1
The contrast of whisker and non-crystal whisker materials
The listed ratio of according to the form below was used opening rubber mixing machine mixing at normal temperatures 20 minutes, obtained the sulfuration composition.
| Carbon black | Common material | Whisker | |
| FE2603 | 100 | 100 | 100 |
| BF6 | 2 | 2 | 2 |
| BPP | 0.6 | 0.6 | 0.6 |
| MgO | 3 | 3 | 3 |
| Ca(OH) 2 | 6 | 6 | 6 |
| N990 | 30 | 10 | 10 |
| BaSO 4 | 20 | ||
| Tismo?D | 20 |
Then, use chromed hardened metal die, at moulding pressure 25kg/cm
2, 170 ℃ of pressed temperatures condition under press vulcanization 10 minutes, shape the test piece of 150 * 150 * 2mm, and by 230C * 16 hour post vulcanization test performance afterwards
| Carbon black | Common material | Whisker | |
| 100% modulus, MPa | 6.1 | 5.2 | 12.2 |
| Tensile strength, MPa | 14.6 | 13.8 | 18.4 |
| Elongation % | 180 | 210 | 150 |
| Hardness, Shao Shi A | 79 | 71 | 79 |
By the data in the last table as can be known, in viton, add 100% modulus and the tensile strength that the pottery whisker can improve fluoro-rubber composite significantly, reduced elongation % simultaneously.
Embodiment 2:
Use/do not use the contrast of fluorochemical surfactant
The listed ratio of according to the form below was used opening rubber mixing machine mixing at normal temperatures 20 minutes, obtained the sulfurized fluoro-rubber composite.
| Blank | Add tensio-active agent | Add tensio-active agent | |
| ML11 | 100 | 100 | 100 |
| BF6 | 2 | 2 | 2 |
| BPP | 0.6 | 0.6 | 0.6 |
| MgO | 6 | 6 | 6 |
| Ca(OH)2 | 6 | 6 | 6 |
| N990 | 10 | 10 | 10 |
| Tismo?D | 20 | 20 | 20 |
| Tensio-active agent | -- | 0.5 | 1 |
Then, use chromed hardened metal die, at moulding pressure 25kg/cm
2, 170 ℃ of pressed temperatures condition under press vulcanization 10 minutes, shape the test piece of 150 * 150 * 2mm, and by 230C * 16 hour post vulcanization test performance afterwards.
| Blank | Add tensio-active agent | Add tensio-active agent | |
| 100% modulus, MPa | 11.6 | 11.4 | 11.5 |
| Tensile strength, MPa | 15.4 | 16.2 | 17.6 |
| Elongation % | 160 | 170 | 180 |
| Hardness, Shao Shi A | 79 | 78 | 79 |
By the data in the last table as can be known, in viton, add tensile strength and the elongation % that fluorochemical surfactant can improve fluoro-rubber composite.
Claims (4)
1. fluoro-rubber composite, it is characterized in that, it comprises 100 weight part viton, the nonmetal whisker of 5-50 weight part, 0.1-5 the vulcanizing agent of the tensio-active agent of weight part and 0.05-10 weight part, it is viton that described viton is selected from biasfluoroethylene-hexafluoropropylene, vinylidene-hexafluoropropylene (HFP)/tetrafluoroethylene (TFE) is a viton, vinylidene-trifluorochloroethylene is a viton, tetrafluoroethylene-propylene is a viton, R 1216-ethene is viton, perfluoroalkyl vinyl ether-ethylene series viton, fluorosilicone is that viton and fluorine phosphine piperazine are viton, described tensio-active agent is a fluorochemical surfactant, described nonmetal whisker is meant the pottery whisker that grows into the monocrystalline form under the manual control condition, its diameter is the 0.2-2 micron, length is the 10-50 micron, described pottery whisker is the carborundum whisker, silicon nitride crystal whisker, mullite crystal whisker, potassium titanate crystal whisker, aluminium borate whisker, ZnOw, magnesia crystal whisker, calcium sulfate crystal whiskers, calcium carbonate crystal whisker, magnesium salt whisker or their mixture, described vulcanizing agent is selected from organo-peroxide, polyol, polyamine compounds and multi-thioalcohol compound.
2. fluoro-rubber composite as claimed in claim 1 is characterized in that, the molecular weight that described viton is measured with the gel infiltration method is 3,000-1,200,000.
3. fluoro-rubber composite as claimed in claim 1 is characterized in that, described fluorochemical surfactant is the perfluoroalkyl sulfone amide derivative.
4. the moulded products that behind sulfidization molding, makes of the described composition of claim 1.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2006100258625A CN100455624C (en) | 2006-04-20 | 2006-04-20 | Fluororubber composition and molding articles |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2006100258625A CN100455624C (en) | 2006-04-20 | 2006-04-20 | Fluororubber composition and molding articles |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN101058657A CN101058657A (en) | 2007-10-24 |
| CN100455624C true CN100455624C (en) | 2009-01-28 |
Family
ID=38864971
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNB2006100258625A Expired - Fee Related CN100455624C (en) | 2006-04-20 | 2006-04-20 | Fluororubber composition and molding articles |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN100455624C (en) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103387682B (en) * | 2013-04-16 | 2015-05-13 | 西安交通大学 | Preparation method for crosslinkable high voltage-resistant high-energy density polyvinylidene fluoride (PVDF) plastic film |
| CN104356563B (en) * | 2014-11-17 | 2016-05-25 | 中昊晨光化工研究院有限公司 | The fluororubber compounded rubber of high temperature high voltage resistant and water vapour |
| CN105419178A (en) * | 2015-11-30 | 2016-03-23 | 安徽锦洋氟化学有限公司 | Fluororubber material used for seal gaskets of engines |
| JP6927319B2 (en) * | 2017-10-18 | 2021-08-25 | ダイキン工業株式会社 | Crosslinkable elastomer composition and fluororubber molded product |
| CN108178892B (en) * | 2018-02-05 | 2020-10-23 | 青岛科技大学 | High-strength low-pressure variable fluororubber material and preparation method thereof |
| CN110229446A (en) * | 2019-06-27 | 2019-09-13 | 西安向阳航天材料股份有限公司 | A kind of vacuum drying tank fluorubber and preparation method thereof |
| CN112745612A (en) * | 2020-07-30 | 2021-05-04 | 台州恩普密封件有限公司 | Ultrahigh-speed dry-grinding-resistant fluororubber oil seal material and preparation method thereof |
| CN114827873B (en) * | 2021-01-29 | 2023-07-14 | 歌尔股份有限公司 | Vibrating diaphragm and sound producing device |
| CN115819902B (en) * | 2022-12-23 | 2023-08-29 | 广东硕成科技股份有限公司 | High-heat-resistance fluororubber material and application thereof |
| CN116856077A (en) * | 2023-07-18 | 2023-10-10 | 苏州大学 | Elastic phase change fiber and preparation method thereof |
| CN117004122A (en) * | 2023-09-04 | 2023-11-07 | 吴江市拓研电子材料有限公司 | High-temperature-resistant oil-resistant teflon ribbon and preparation method thereof |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH02206639A (en) * | 1989-02-03 | 1990-08-16 | Nok Corp | Fluororubber composition |
| JP2000290527A (en) * | 1999-04-06 | 2000-10-17 | Shikoku Chem Corp | Surface-modified aluminum borate whisker and resin composition containing it |
| WO2005042636A1 (en) * | 2003-10-31 | 2005-05-12 | Junkosha Inc. | Fluororesin compositions |
| CN1732221A (en) * | 2002-12-27 | 2006-02-08 | 杜邦·三井氟化学株式会社 | Fluororesin composition |
-
2006
- 2006-04-20 CN CNB2006100258625A patent/CN100455624C/en not_active Expired - Fee Related
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH02206639A (en) * | 1989-02-03 | 1990-08-16 | Nok Corp | Fluororubber composition |
| JP2000290527A (en) * | 1999-04-06 | 2000-10-17 | Shikoku Chem Corp | Surface-modified aluminum borate whisker and resin composition containing it |
| CN1732221A (en) * | 2002-12-27 | 2006-02-08 | 杜邦·三井氟化学株式会社 | Fluororesin composition |
| WO2005042636A1 (en) * | 2003-10-31 | 2005-05-12 | Junkosha Inc. | Fluororesin compositions |
Non-Patent Citations (2)
| Title |
|---|
| 钛酸钾晶须增强聚四氟乙烯复合材料的摩擦磨损性能. 冯新，陈东辉等.高分子材料科学与工程，第20卷第5期. 2004 |
| 钛酸钾晶须增强聚四氟乙烯复合材料的摩擦磨损性能. 冯新，陈东辉等.高分子材料科学与工程，第20卷第5期. 2004 * |
Also Published As
| Publication number | Publication date |
|---|---|
| CN101058657A (en) | 2007-10-24 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN100455624C (en) | Fluororubber composition and molding articles | |
| CN1104464C (en) | Fluororubber composition and molding thereof | |
| KR101419956B1 (en) | Rubber composition and method for producing the same, seal member by using the same and apparatus having the same, and a rubber composition for resistance to dme | |
| CN104662084B (en) | Fluoro-rubber composite | |
| KR101522262B1 (en) | Lip seal for water pump | |
| US5374484A (en) | Fluorine-containing elastomer composition and molded articles made therefrom | |
| US6416840B1 (en) | Fluorine-containing meltable resin composition | |
| US10793706B2 (en) | Fluororubber composition | |
| JP7223013B2 (en) | Copolymer of chloroprene monomer and unsaturated nitrile compound, composition containing copolymer, vulcanized molded article of composition, and use of vulcanized molded article | |
| CN101307165A (en) | Heat resisting fluororubber composition and sulfidization molding products thereof | |
| CN107001751B (en) | Fluoro-rubber composite and crosslinked fluororubber article | |
| CN100420875C (en) | A toothed belt | |
| US3282902A (en) | Curable polysulfide compositions, methods and vulcanizates | |
| EP3143083A1 (en) | Ester plasticizers based on renewable raw materials for elastomers | |
| JPH06157686A (en) | Fluoroelastomer composition and its molded product | |
| US5587413A (en) | Fluorine rubber composition | |
| Chapurkin et al. | Features of the structure formation of fluoroelastomers by fluoroperoxides | |
| US4431776A (en) | Fast-curing olefin copolymer rubber compositions | |
| CN114746499A (en) | Flame retardant polymer composition | |
| CN115803383A (en) | Fluororubber composition | |
| CN117683308A (en) | Fluororubber composition | |
| JP2010235907A (en) | Fluororubber composition and rubber molding using the same | |
| JPH07310069A (en) | Silicone rubber composition for sealing | |
| Cardarelli | Polymers and elastomers | |
| Donskoi et al. | Polysulfide and organosilicon low-molecular-mass rubbers and sealants on their basis |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant | ||
| CF01 | Termination of patent right due to non-payment of annual fee | ||
| CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20090128 |