CN104761756A - Suspension buffer dust cover and preparation method thereof - Google Patents
Suspension buffer dust cover and preparation method thereof Download PDFInfo
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- CN104761756A CN104761756A CN201410395662.3A CN201410395662A CN104761756A CN 104761756 A CN104761756 A CN 104761756A CN 201410395662 A CN201410395662 A CN 201410395662A CN 104761756 A CN104761756 A CN 104761756A
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L7/00—Compositions of natural rubber
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29B—PREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
- B29B7/00—Mixing; Kneading
- B29B7/02—Mixing; Kneading non-continuous, with mechanical mixing or kneading devices, i.e. batch type
- B29B7/22—Component parts, details or accessories; Auxiliary operations
- B29B7/28—Component parts, details or accessories; Auxiliary operations for measuring, controlling or regulating, e.g. viscosity control
- B29B7/286—Component parts, details or accessories; Auxiliary operations for measuring, controlling or regulating, e.g. viscosity control measuring properties of the mixture, e.g. temperature, density
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C35/00—Heating, cooling or curing, e.g. crosslinking or vulcanising; Apparatus therefor
- B29C35/02—Heating or curing, e.g. crosslinking or vulcanizing during moulding, e.g. in a mould
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/03—Polymer mixtures characterised by other features containing three or more polymers in a blend
- C08L2205/035—Polymer mixtures characterised by other features containing three or more polymers in a blend containing four or more polymers in a blend
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Physics & Mathematics (AREA)
- Oral & Maxillofacial Surgery (AREA)
- Thermal Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
The invention provides a suspension buffer dust cover and a preparation method thereof. The suspension buffer dust cover comprises, by weight, the natural rubber 20 parts of, 80 parts of ethylene propylene terpolymer, 50-90 parts of carbon black, 2-10 parts of a lubricant, 2-10 parts of fatty acid, 4.5-8.5 parts of a surfactant, 0.6-1 part of peroxide, 0.5-1 part of sulfur, 2-4 parts of a promoter and 3-7 parts of an antioxidant. The suspension buffer dust cover of the invention has the advantages of good elasticity, good mechanical strength, small permanent deformation, wear resistance and excellent heat resistance. A preparation method is as below: respectively mixing natural rubber and ethylene propylene terpolymer, and blending the two, so as to achieve co-vulcanization of rubber compound with a composite vulcanization system containing sulfur, peroxide and promoter. The dust cover parts of the prepared suspension buffer dust cover have good heat resistance and ozone resistance, and a buffer spring pad part also has good shock absorption performance and anti-fatigue performance, and solves the defects of integrated structure of the spring pad and the dust cover.
Description
Technical field
The present invention relates to automobile chassis suspension systems technology field, particularly relate to a kind of rack buffer dw and preparation method thereof.
Background technology
Automobile chassis suspension system is one of key components and parts affecting car comfort, and its effect is the force and moment transmitting vehicle frame and axletree; Relax the shock load that vehicle frame is passed on road surface, the vibration of the load system caused thus of decaying, ensures ride of vehicle; Ensure that wheel has desirable motion characteristics when Uneven road and load change, ensure the control stability of automobile; Rack buffer dw is for chassis suspension system, and when automobile turning, travel and jolt in the moving processes such as road conditions, mainly play the effects such as supports, location, buffering, absorbing and noise reduction, improvement is handling, comfortableness and stability by bus.
Existing factory is saving material cost and assembly cost, by spring pad and dust boot design integralization structure.Spring pad position requires that product has good elasticity and damping performance, and dw position needs good aging resistance and ozone resistance.When this series products adopted natural rubber to make in the past, there is dw position and easily lost efficacy because thermotolerance is not high and ozone resistance is poor; When adopting terpolymer EP rubber to make, damping performance and the fatigue endurance performance at its spring pad position can not meet the demands and lose efficacy again.
Summary of the invention
In view of this, one aspect of the present invention provides a kind of rack buffer dw, while the dw position of this suspension dw has good thermotolerance and ozone resistants, the spring pad position of rack buffer dw also has good damping performance and fatigue performance, the invention solves the defect problem by spring pad and dust boot design integralization structure.
For reaching this object, the present invention by the following technical solutions:
A kind of rack buffer dw, by weight, comprises following component:
Preferably, this rack buffer dw also comprises dispersion agent 2 ~ 6 parts, scorch retarder 0.2 ~ 0.6 part, sulfuration resistant reductive agent 0.5 ~ 0.8 part.
Preferably, promotor is made up of vulkacit D TDM1 ~ 2 part, accelerant CZ 1 ~ 2 part, and anti-aging agent is made up of antioxidant 4020 1 ~ 3 part, anti-aging agent RD 2 ~ 4 parts, and promoting agent is made up of indirect process zinc oxide 4 ~ 6 parts, stearic acid 0.5 ~ 2.5 part.
Stearic acid plays an important role in the synthesis and the course of processing of rubber.Stearic acid is the vulcanization leveller of widespread use in natural rubber, synthetic rubber and latex.
Indirect process zinc oxide, take zinc ingot metal as raw material, zinc ingot metal is converted to zinc fume in plumbago crucible under the high temperature of 1000 DEG C, is generated zinc oxide subsequently, and after cooling tube, collect to obtain Zinc oxide particles by the atmospheric oxidation blasted.Can be used as vulcanization of rubber promoting agent, strengthening agent.
DTDM name is called 4,4`-dimorpholinyl disulfide, it can be used as the effective promotor of sulfur cross-linking of natural gum and synthetical glue, and it is high that its cross-linked rubber has mechanical property, and ozone resistance is high, the advantage of the good and rubber unvulcanizate of ozone resistance not incipient scorch, especially good with sulfenamide type accelerators combined effect, there is outstanding heat-resistant aging, no blooming, and compression set is little, can be used in tire and technical rubber goods.
Accelerant CZ name is called N-cyclohexyl-2-benzothiazole sulfonamide, and CZ is the aftereffect promotor that a kind of height is active, and scorching quality is excellent, process safety, curing time is short, and when curing temperature more than 138 DEG C, promoter action is very strong, often coordinates work second promotor with DTDM promotor.
Anti-aging agent refers to prevent or suppress the factors disrupt product propertiess such as such as oxygen, heat, light, ozone, mechanical stress, heavy metal ion, extend goods storage and the Synergist S-421 95 in work-ing life, and the aging protection effect caused heat and oxygen is splendid.Anti-aging agent RD is 2,2,4-trimethylammonium-1,2-dihyaroquinoline polymer; 2,2,4 trimethyl 1,2 dihydroquinoline polymer; The homopolymer of 1,2-dihydro-2,2,4-trimethylquinoline; 2,2,4-trimethylammonium-1,2-dihyaroquinoline.RD and 4020 with making goods have ozone-resistant and anti-flexing fatigue performance.Antioxidant 4020 name is called N-(1,3-dimethyl) butyl-N'-diphenyl-para-phenylene diamine, natural rubber and use for synthetic rubber antiozonidate and oxidation inhibitor, to ozone-induced cracking and the aging protective benefits of flexing fatigue excellent, also have good protective effect to heat, oxygen and the poisonous metal such as copper, manganese.
Preferably, carbon black is carbon black N-330, and dispersion agent is that a part T moulded by Lay mattress, and lubricant is paraffin B-10, and scorch retarder is anti-scorching agent CTP, and superoxide is DCP, and sulphur is insoluble sulfur IS-60, and sulfuration resistant reductive agent is SR534D.
Carbon black N330 belongs to high abrasion furnace black(HAF), is the high wearable carbon black be most widely used.This product wear resistance is better than thermally oxidized black, meanwhile, is the carbon black that a kind of reinforcing property is good, can gives the good tensile property of sizing material, tear resistance, wear resistance and elasticity.Carbon black N330 disperses and tubing properties in sizing material, is applicable to various synthetic rubber and natural rubber.
Part T moulded by dispersion agent Lay mattress can make sizing material fully disperse, and paraffin has good lubricant effect, and paraffin of the present invention is B-10 model.
Anti-scorching agent CTP, formal name used at school N-cyclohexylthiophthalimide, can be used for natural rubber and synthetic rubber, can effectively prevent sizing material from the course of processing, incipient scorch occurring, enhance productivity; Simultaneously for standing Gao Re or having the sizing material of slight incipient scorch to have reactivation.
DCP is called dicumyl peroxide (dicumyl peroxide), peroxidation two cumin.Be a kind of strong oxidizer, use the rubber of DCP to have excellent insulativity and processing characteristics, and its thermotolerance can be improved.
Insoluble sulfur (Insoluble Sulfur) is a kind of nontoxic, flammable yellow powder.It obtains through common sulphur thermopolymerization, and the number of sulfur atoms on molecular chain, up to more than 108, has visco-elasticity and the molecular weight distribution of superpolymer, therefore also claims plastic sulfur or polymerised sulphur.Insoluble sulfur has the following advantages: dispersed in sizing material, effectively resists the gathering of sulphur, reduces the incipient scorch tendency that process deposited by sizing material; Make rubber non-migratory phenomenon in adjacent glue-line; Insoluble sulfur shortens the time of sulfuration, and after reaching curing temperature, it has one " activation stage ", i.e. chain type unzipping makes vulcanization rate accelerate, and reduces sulfur consumption, is conducive to the improvement of goods aging resistance.The present invention uses insoluble sulfur IS-60.
Sulfuration resistant reductive agent SR534D is polyfunctional acrylic ester compounds, compensates the polysulfide crosslink bond lost because of reduction, thus keep the cross-linking density of sizing material when reduction occurs in sulfuration by forming carbon-carbon crosslink.There is reversion in the place that can effectively prevent product thinner, keeps higher mechanical property.
Preferably, this rack buffer dw, by weight, comprises following component:
The present invention provides a kind of method preparing above-mentioned rack buffer dw on the other hand, this preparation method adopts respectively that natural rubber, terpolymer EP rubber is mixing and it is blended, the covulcanization of rubber unvulcanizate is reached with the compounded curing system of sulphur, superoxide, promotor, the dw position of the rack buffer dw prepared is made to have good thermotolerance and ozone resistants, the spring pad position of rack buffer dw also has good damping performance and fatigue performance simultaneously, solves the defect problem of spring pad and dust boot design integralization structure.
Prepare a method for above-mentioned rack buffer dw, comprise the following steps:
(1) by weight, 100 parts of natural rubbers, carbon black 50 ~ 90 parts, lubricant paraffin B-102 ~ 10 part, 2 ~ 10 parts, lipid acid, promoting agent indirect process zinc oxide 4 ~ 6 parts, promoting agent stearic acid 0.5 ~ 2.5 part, anti-aging agent RD 2 ~ 4 parts, antioxidant 4020 1 ~ 3 part, vulkacit D TDM1 ~ 2 part, accelerant CZ 1 ~ 2 part, 0.5 ~ 1 part, sulphur, Lay mattress are moulded part T2 ~ 6 part, scorch retarder 0.2 ~ 0.6 part, sulfuration resistant reductive agent 0.7 ~ 1 part carry out mixing on a mill until, obtained natural rubber masterbatch;
100 parts of terpolymer EP rubbers, carbon black 50 ~ 90 parts, lubricant paraffin B-102 ~ 10 part, 2 ~ 10 parts, lipid acid, promoting agent indirect process zinc oxide 4 ~ 6 parts, promoting agent stearic acid 0.5 ~ 2.5 part, anti-aging agent RD 2 ~ 4 parts, antioxidant 4020 1 ~ 3 part, vulkacit D TDM1 ~ 2 part, accelerant CZ 1 ~ 2 part, 0.5 ~ 1 part, sulphur, Lay mattress are moulded part T2 ~ 6 part, scorch retarder 0.2 ~ 0.6 part, superoxide 0.6 ~ 1 part carry out mixing on a mill until, obtained terpolymer EP rubber master batch;
(2) terpolymer EP rubber master batch is carried out prevulcanized in Banbury mixer, obtain terpolymer EP rubber prevulcanized glue;
(3) natural rubber masterbatch and terpolymer EP rubber prevulcanized glue are carried out blended according to mass ratio 4:1 in Banbury mixer, then binder removal, obtained strip profiled member on preform machine;
(4) barrel strip profiled member being put into injection vulcanizer carries out sulfidizing, and finally cooling, deburring obtains rack buffer dw.
In rubber compounding process, first natural rubber and terpolymer EP rubber are made master batch respectively, after the master batch of terpolymer EP rubber is carried out prevulcanized, obtained terpolymer EP rubber prevulcanized glue, finally by natural master batch and terpolymer EP rubber prevulcanized glue blended, adopt such calendering process can ensure effective covulcanization of natural rubber and terpolymer EP rubber, thus obtain excellent material property.The present invention adopts the compounded curing system of sulphur, superoxide, promotor, and under this system, rubber unvulcanizate has good comprehensive tool performance and heat aging performance.
Preferably, in step (1), natural rubber and terpolymer EP rubber melting temperature are 50 ~ 60 DEG C, and mixing time is 30 ~ 40min.
Preferably, in step (2), pre-curing temperature is 150 ~ 160 DEG C, and prevulcanisation time is 5 ~ 10min.
Preferably, in step (3), dump temperature is 100 ~ 105 DEG C.
Preferably, the middle sulfidizing of step (4) is at pressure 170 ~ 190Kgf/cm
2, carry out under temperature 160 ~ 170 DEG C of conditions, curing time is 240-360 second.
Compared with prior art, beneficial effect of the present invention is: rack buffer dw of the present invention, by weight, natural rubber 80 parts, terpolymer EP rubber 20 parts, carbon black 50 ~ 90 parts, lubricant 2 ~ 10 parts, 2 ~ 10 parts, lipid acid, promoting agent 4.5 ~ 8.5 parts, superoxide 0.6 ~ 1 part, 0.5 ~ 1 part, sulphur, promotor 2 ~ 4 parts, 3 ~ 7 parts, anti-aging agent is comprised.Rack buffer dw of the present invention has that elasticity is good, physical strength good, tension set is little, wear resistance is good, the advantage of Good Heat-resistance, long service life; Preparation method of the present invention adopts respectively that natural rubber, terpolymer EP rubber is mixing and it is blended, the covulcanization of rubber unvulcanizate is reached with the compounded curing system of sulphur, superoxide, promotor, the dw position of the rack buffer dw prepared is made to have good thermotolerance and ozone resistants, the spring pad position of rack buffer dw also has good damping performance and fatigue performance simultaneously, solves the defect problem of spring pad and dust boot design integralization structure.
Embodiment
Further illustrate technical scheme of the present invention respectively below in conjunction with the embodiments.
Raw material involved in following examples is commercially available.
Embodiment 1: the rack buffer dw of the present embodiment, by weight, comprises following component:
The preparation method of the rack buffer dw of the present embodiment, comprises the following steps:
(1) by weight, 100 parts of natural rubbers, carbon black N330 50 parts, paraffin B-10 2 parts, 8 parts, lipid acid, indirect process zinc oxide 5 parts, stearic acid 1 part, anti-aging agent RD 2 parts, antioxidant 4020 2.5 parts, vulkacit D TDM1 part, accelerant CZ 1 part, insoluble sulfur IS-60 0.5 part, Lay mattress are moulded a part T5 part, anti-scorching agent CTP 0.5 part, sulfuration resistant reductive agent SR534D0.8 part carries out mixing on a mill until, mixing 30min, obtained natural rubber masterbatch;
100 parts of terpolymer EP rubbers, carbon black N330 50 parts, paraffin B-10 2 parts, 8 parts, lipid acid, indirect process zinc oxide 5 parts, stearic acid 1 part, anti-aging agent RD 2 parts, antioxidant 4020 2.5 parts, vulkacit D TDM1 part, accelerant CZ 1 part, insoluble sulfur IS-60 0.5 part, Lay mattress are moulded a part T5 part, anti-scorching agent CTP 0.5 part, superoxide DCP0.8 part carries out mixing on a mill until, mixing 30min, obtained terpolymer EP rubber master batch;
(2) above-mentioned terpolymer EP rubber master batch to be dropped in Banbury mixer prevulcanized 5min at 150 DEG C, obtain terpolymer EP rubber prevulcanized glue;
(3) natural rubber masterbatch and terpolymer EP rubber prevulcanized glue are carried out blended according to mass ratio 4:1 in Banbury mixer, carry out binder removal at 100 DEG C, then obtained strip profiled member on preform machine;
(4) strip profiled member being put into the barrel of injection vulcanizer, is 170Kgf/cm at pressure
2, temperature is carry out sulfidizing 360 seconds under the condition of 160 DEG C, finally take out cooling, deburring obtain rack buffer dw.
Embodiment 2: the rack buffer dw of the present embodiment, by weight, comprises following component:
In the present embodiment, the preparation method of rack buffer dw is with embodiment 1.
Embodiment 3: the rack buffer dw of the present embodiment, by weight, comprises following component:
In the present embodiment, the preparation method of rack buffer dw is with embodiment 1.
Embodiment 4: the rack buffer dw of the present embodiment, by weight, comprises following component:
In the present embodiment, the preparation method of rack buffer dw is with embodiment 1.
The rack buffer dw obtained in embodiment 1 ~ 4 and existing rack buffer dw (V3R-021) are carried out performance test, and result is as follows:
Can find out that rack buffer dw of the present invention has good springiness, physical strength is high, tension set is little, wear resistance is good, the advantage of Good Heat-resistance by upper table.Product dynamic load is durable simultaneously reaches 1,000,000 times.
Rack buffer dw of the present invention has good elasticity and physical strength, tension set is little, wear resistance good, the advantage of Good Heat-resistance, long service life, the dw position of this rack buffer dw has good thermotolerance and ozone resistants, the spring pad position of rack buffer dw also has good damping performance and fatigue performance simultaneously, solves the defect problem of spring pad and dust boot design integralization structure.
It should be noted that and understand, when not departing from the spirit and scope of accompanying claim the present invention for required protection, various amendment and improvement can be made to the present invention of foregoing detailed description.Therefore, the scope of claimed technical scheme is not by the restriction of given any specific exemplary teachings.
Applicant states, the present invention illustrates detailed process equipment and process flow process of the present invention by above-described embodiment, but the present invention is not limited to above-mentioned detailed process equipment and process flow process, namely do not mean that the present invention must rely on above-mentioned detailed process equipment and process flow process and could implement.Person of ordinary skill in the field should understand, any improvement in the present invention, to equivalence replacement and the interpolation of ancillary component, the concrete way choice etc. of each raw material of product of the present invention, all drops within protection scope of the present invention and open scope.
Claims (10)
1. a rack buffer dw, is characterized in that: by weight, comprises following component:
2. rack buffer dw according to claim 1, is characterized in that: also comprise dispersion agent 2 ~ 6 parts, scorch retarder 0.2 ~ 0.6 part, sulfuration resistant reductive agent 0.5 ~ 0.8 part.
3. rack buffer dw according to claim 1, it is characterized in that: described promotor is made up of vulkacit D TDM1 ~ 2 part, accelerant CZ 1 ~ 2 part, described anti-aging agent is made up of antioxidant 4020 1 ~ 3 part, anti-aging agent RD 2 ~ 4 parts, and described promoting agent is made up of indirect process zinc oxide 4 ~ 6 parts, stearic acid 0.5 ~ 2.5 part.
4. rack buffer dw according to claim 2, it is characterized in that: described carbon black is carbon black N-330, described dispersion agent is that a part T moulded by Lay mattress, described lubricant is paraffin B-10, described scorch retarder is anti-scorching agent CTP, described superoxide is DCP, and described sulphur is insoluble sulfur IS-60, and described sulfuration resistant reductive agent is SR534D.
5. rack buffer dw according to claim 3, is characterized in that: by weight, comprises following component:
6. prepare a method for rack buffer dw as claimed in claim 1, it is characterized in that, comprise the following steps:
(1) by weight, 100 parts of natural rubbers, carbon black 50 ~ 90 parts, lubricant paraffin B-102 ~ 10 part, 2 ~ 10 parts, lipid acid, promoting agent indirect process zinc oxide 4 ~ 6 parts, promoting agent stearic acid 0.5 ~ 2.5 part, anti-aging agent RD 2 ~ 4 parts, antioxidant 4020 1 ~ 3 part, vulkacit D TDM1 ~ 2 part, accelerant CZ 1 ~ 2 part, 0.5 ~ 1 part, sulphur, Lay mattress are moulded part T2 ~ 6 part, scorch retarder 0.2 ~ 0.6 part, sulfuration resistant reductive agent 0.7 ~ 1 part carry out mixing on a mill until, obtained natural rubber masterbatch;
100 parts of terpolymer EP rubbers, carbon black 50 ~ 90 parts, lubricant paraffin B-102 ~ 10 part, 2 ~ 10 parts, lipid acid, promoting agent indirect process zinc oxide 4 ~ 6 parts, promoting agent stearic acid 0.5 ~ 2.5 part, anti-aging agent RD 2 ~ 4 parts, antioxidant 4020 1 ~ 3 part, vulkacit D TDM1 ~ 2 part, accelerant CZ 1 ~ 2 part, 0.5 ~ 1 part, sulphur, Lay mattress are moulded part T2 ~ 6 part, scorch retarder 0.2 ~ 0.6 part, superoxide 0.6 ~ 1 part carry out mixing on a mill until, obtained terpolymer EP rubber master batch;
(2) terpolymer EP rubber master batch is carried out prevulcanized in Banbury mixer, obtain terpolymer EP rubber prevulcanized glue;
(3) natural rubber masterbatch and terpolymer EP rubber prevulcanized glue are carried out blended according to mass ratio 4:1 in Banbury mixer, then binder removal, obtained strip profiled member on preform machine;
(4) barrel strip profiled member being put into injection vulcanizer carries out sulfidizing, and finally cooling, deburring obtains rack buffer dw.
7. preparation method according to claim 6, is characterized in that, in step (1), natural rubber and terpolymer EP rubber melting temperature are 50 ~ 60 DEG C, and mixing time is 30 ~ 40min.
8. preparation method according to claim 6, is characterized in that, in step (2), pre-curing temperature is 150 ~ 160 DEG C, and prevulcanisation time is 5 ~ 10min.
9. preparation method according to claim 6, is characterized in that, in step (3), dump temperature is 100 ~ 105 DEG C.
10. preparation method according to claim 6, is characterized in that, in step (4), sulfidizing is at pressure 170 ~ 190Kgf/cm
2, carry out under temperature 160 ~ 170 DEG C of conditions, curing time is 240-360 second.
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Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
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CN110684243A (en) * | 2019-09-26 | 2020-01-14 | 东莞市铭辉自动化设备有限公司 | Special rubber sleeve composition for grinding and polishing mobile phone glass |
CN115785673A (en) * | 2022-12-01 | 2023-03-14 | 浙江创城高分子材料有限公司 | Natural rubber composition and rubber product for dust cover |
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CN101585936A (en) * | 2009-02-20 | 2009-11-25 | 山东美晨科技股份有限公司 | A kind of automobile rubber support formulation |
CN102705411A (en) * | 2012-06-01 | 2012-10-03 | 安徽微威胶件集团有限公司 | Ozone-resisting supporting rubber vibration absorber of truck cab and preparation method of ozone-resisting supporting rubber vibration absorber |
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2014
- 2014-08-12 CN CN201410395662.3A patent/CN104761756A/en active Pending
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
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CN101585936A (en) * | 2009-02-20 | 2009-11-25 | 山东美晨科技股份有限公司 | A kind of automobile rubber support formulation |
CN102705411A (en) * | 2012-06-01 | 2012-10-03 | 安徽微威胶件集团有限公司 | Ozone-resisting supporting rubber vibration absorber of truck cab and preparation method of ozone-resisting supporting rubber vibration absorber |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
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CN110684243A (en) * | 2019-09-26 | 2020-01-14 | 东莞市铭辉自动化设备有限公司 | Special rubber sleeve composition for grinding and polishing mobile phone glass |
CN115785673A (en) * | 2022-12-01 | 2023-03-14 | 浙江创城高分子材料有限公司 | Natural rubber composition and rubber product for dust cover |
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Application publication date: 20150708 |