CN106566028A - Anti-wear rubber and preparation method thereof - Google Patents

Anti-wear rubber and preparation method thereof Download PDF

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Publication number
CN106566028A
CN106566028A CN201610953006.XA CN201610953006A CN106566028A CN 106566028 A CN106566028 A CN 106566028A CN 201610953006 A CN201610953006 A CN 201610953006A CN 106566028 A CN106566028 A CN 106566028A
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parts
rubber
abrasive rubber
coupling agent
abrasive
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殳斌
肖维
张成兵
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Tongxiang Spring Rubber & Plastics Tech Co Ltd
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Tongxiang Spring Rubber & Plastics Tech Co Ltd
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    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K13/00Use of mixtures of ingredients not covered by one single of the preceding main groups, each of these compounds being essential
    • C08K13/02Organic and inorganic ingredients
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/02Elements
    • C08K3/08Metals
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/18Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/20Oxides; Hydroxides
    • C08K3/22Oxides; Hydroxides of metals
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/04Oxygen-containing compounds
    • C08K5/09Carboxylic acids; Metal salts thereof; Anhydrides thereof
    • C08K5/098Metal salts of carboxylic acids
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/04Oxygen-containing compounds
    • C08K5/10Esters; Ether-esters
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/04Oxygen-containing compounds
    • C08K5/14Peroxides
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/36Sulfur-, selenium-, or tellurium-containing compounds
    • C08K5/39Thiocarbamic acids; Derivatives thereof, e.g. dithiocarbamates
    • C08K5/40Thiurams, i.e. compounds containing groups
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/36Sulfur-, selenium-, or tellurium-containing compounds
    • C08K5/43Compounds containing sulfur bound to nitrogen
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L7/00Compositions of natural rubber
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L9/00Compositions of homopolymers or copolymers of conjugated diene hydrocarbons
    • C08L9/02Copolymers with acrylonitrile
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/02Elements
    • C08K3/08Metals
    • C08K2003/0893Zinc
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/18Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/20Oxides; Hydroxides
    • C08K3/22Oxides; Hydroxides of metals
    • C08K2003/2217Oxides; Hydroxides of metals of magnesium
    • C08K2003/222Magnesia, i.e. magnesium oxide
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/18Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/20Oxides; Hydroxides
    • C08K3/22Oxides; Hydroxides of metals
    • C08K2003/2296Oxides; Hydroxides of metals of zinc
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K2201/00Specific properties of additives
    • C08K2201/014Additives containing two or more different additives of the same subgroup in C08K
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2201/00Properties
    • C08L2201/08Stabilised against heat, light or radiation or oxydation
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2205/00Polymer mixtures characterised by other features
    • C08L2205/03Polymer mixtures characterised by other features containing three or more polymers in a blend

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  • 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

The invention discloses anti-wear rubber and a preparation method thereof. The anti-wear rubber includes, by weight, 100 parts of raw rubber, 1-2 parts of zinc oxide, 3-10 parts of stearic acid, 1-3 parts of a vulcanizer, 2-5 parts of an accelerator, 50-100 parts of carbon black, 3-10 parts of magnesium oxide, 1-3 parts of an anti-aging agent, 5-10 parts of zinc powder, 3-10 parts of magnesium methacrylate, 5-10 parts of oligomer ester, and 1-3 parts of a coupling agent. The rubber has excellent anti-wear property and heat resistance.

Description

A kind of abrasive rubber and preparation method thereof
Technical field
The present invention relates to technical field of rubber production, more particularly to a kind of abrasive rubber and preparation method thereof.
Background technology
Rubber is a kind of polymer of reversible deformation.Rubber high resilience at room temperature, the external force for giving very little is acted on just Very big deformation can be produced, original state can be returned to again after external force is removed.Based on rubber industry industry it One, occupy an important position in the national economy of China.And the aspect such as daily, medical for us provides substantial amounts of light industry Rubber product, and provide various rubber system productions for the heavy industry such as digging, traffic, building, machinery, electronics and new industry Equipment or rubber components.It can be seen that, rubber is in our productive lifes using quite varied.
Developing rapidly for economy and gradually going deep into for mineral exploration and exploitation depth, propose to the anti-wear performance of engineering parts Huge challenge.Although in many developed countries, as Japan, the U.S., Europe etc., abrasive rubber has obtained the wide use sent out, It is that its technical formula is all kept absolutely secret.Therefore, a kind of preparation method of abrasive rubber is found for Chinese national economy Development and the exploitation of mining industry are just particularly important.
The content of the invention
It is an object of the invention to provide a kind of abrasive rubber, has and has good wearability and heat resistance.
Present invention also offers the preparation method of above-mentioned abrasive rubber.
The technical solution adopted for the present invention to solve the technical problems is:
A kind of abrasive rubber, the raw material of the abrasive rubber includes by weight following components:100 parts of rubber, zinc oxide 1- 2 parts, hard acid fat 3-10 parts, vulcanizing agent 1-3 parts, accelerator 2-5 parts, carbon black 50-100 parts, magnesia 3-10 parts, age resistor 1-3 parts, zinc powder 5-10 parts, magnesinm methacrylate 3-10 parts, oligomer ester 5-10 parts, coupling agent 1-3 parts.
Preferably, the raw material of the abrasive rubber also includes by weight abrasion resistance modifier 3-5 parts.The present invention passes through Addition abrasion resistance modifier, further increases anti-wear performance, improves resistance to elevated temperatures.
Preferably, the abrasion resistance modifier is made up by weight of following raw material:15-20 part polyamic acids, 3-5 parts Glass microballoon, 5-8 part Graphenes, 3-5 part bortz powders, 1-2 part Silane coupling agent KH550s, 30-50 part DMF.Glass microballoon+ The combination of Graphene+bortz powder can effectively improve anti-wear performance, and improve resistance to elevated temperatures.It is micro- to glass using polyamic acid The combination of pearl+Graphene+bortz powder is modified, high with the bond strength of rubber matrix.
Preferably, the preparation method of the anti-wear agent is:Polyamic acid is mixed with DMF, is heated and is stirred to polyamides Amino acid is completely dissolved, and is subsequently adding glass microballoon, silicon powder, bortz powder and Silane coupling agent KH550, is uniformly mixed, It is cooled to room temperature.
Preferably, the rubber is one or two in nitrile rubber, natural rubber.
Preferably, the accelerator is tetramethyl thiuram disulfide and 4, the mixture of 4 '-dithio morpholine.
Preferably, the vulcanizing agent is cumyl peroxide.
Preferably, the coupling agent is silane coupler KH560, silane coupler KH570, silane coupler KH590 In one or more.
A kind of preparation method of abrasive rubber, step is as follows:
1)First rubber is plasticated using banbury, plasticating temperature is 40-80 DEG C;
2)Then by step 1)It is rubber, zinc oxide, zinc powder, magnesinm methacrylate, hard acid fat, carbon black, magnesia after process, neat Polyester, coupling agent, accelerator and age resistor, are then kneaded using banbury, and melting temperature is 40 DEG C -80 DEG C;
3)Vulcanizing agent is added, is then turned refining again, finally vulcanized, curing temperature is 140-160 DEG C.
A kind of preparation method of abrasive rubber, step is as follows:
1)First rubber is plasticated using banbury, plasticating temperature is 40-80 DEG C;
2)Then by step 1)It is rubber, zinc oxide, zinc powder, magnesinm methacrylate, hard acid fat, carbon black, magnesia after process, neat Polyester, coupling agent, accelerator, age resistor and abrasion resistance modifier, are then kneaded using banbury, melting temperature be 40 DEG C- 80℃;
3)Vulcanizing agent is added, is then turned refining again, finally vulcanized, curing temperature is 140-160 DEG C.
The invention has the beneficial effects as follows:
1)The rubber that the preparation method is adopted is mainly nitrile rubber, natural rubber or the two is compound, and is additionally added The compositions such as magnesia, zinc oxide, zinc powder and methyl methacrylate magnesium, tool has good wearability and higher hardness.
2)Using DCP/TMTD/DTDM blending vulcanization systems, sizing material hot tear crack performance is improved, comprehensive physical mechanicalness Can improve.
3)Add oligomer ester and magnesinm methacrylate and zinc powder, can effectively improve the heat resistance of product, hardness and Wearability.
Specific embodiment
Below by specific embodiment, technical scheme is described in further detail.
In the present invention, if not refering in particular to, the raw material for being adopted and equipment etc. are commercially available or commonly used in the art. Method in following embodiments, if no special instructions, is the conventional method of this area.
Embodiment 1:
A kind of abrasive rubber, the raw material of the abrasive rubber includes by weight following components:Rubber(Nitrile rubber)100 Part, 1 part of zinc oxide, 3 parts of hard acid fat, vulcanizing agent(DCP)1 part, accelerator(1 part of 1 part of TMTD, DTDM)2 parts, 50 parts of carbon black, 3 parts of magnesia, age resistor(Anti-aging agent RD)1 part, 10 parts of zinc powder, 10 parts of magnesinm methacrylate, 5 parts of oligomer ester, coupling agent(Silane Coupling agent KH590)1 part.
Embodiment 2:
A kind of abrasive rubber, the raw material of the abrasive rubber includes by weight following components:Rubber(Natural rubber)100 Part, 2 parts of zinc oxide, 10 parts of hard acid fat, vulcanizing agent(DCP)3 parts, accelerator(3 parts of 2 parts of TMTD, DTDM)5 parts, carbon black 100 Part, 10 parts of magnesia, age resistor(Anti-aging agent RD)3 parts, 5 parts of zinc powder, 3 parts of magnesinm methacrylate, 10 parts of oligomer ester is coupled Agent(Silane coupler KH560)3 parts.
Embodiment 3:
A kind of abrasive rubber, the raw material of the abrasive rubber includes by weight following components:Rubber(50 parts of nitrile rubber+ 50 parts of natural rubber)100 parts, 1.5 parts of zinc oxide, 5 parts of hard acid fat, vulcanizing agent(DCP)2 parts, accelerator(2 parts of TMTD, 1 part of DTDM)3 parts, 60 parts of carbon black, 5 parts of magnesia, age resistor(Anti-aging agent RD)2 parts, 7 parts of zinc powder, magnesinm methacrylate 5 Part, 8 parts of oligomer ester, coupling agent(Silane coupler KH590)2 parts.
The preparation method step of embodiment 1-3 is as follows:
1)First rubber is plasticated using banbury, plasticating temperature is 40-80 DEG C;
2)Then by step 1)It is rubber, zinc oxide, zinc powder, magnesinm methacrylate, hard acid fat, carbon black, magnesia after process, neat Polyester, coupling agent, accelerator and age resistor, are then kneaded using banbury, and melting temperature is 40 DEG C -80 DEG C;
3)Vulcanizing agent is added, is then turned refining again, finally vulcanized, curing temperature is 140-160 DEG C.
Embodiment 4:
The present embodiment is also added with 5 parts of abrasion resistance modifiers on the basis of the formula of embodiment 1.
The abrasion resistance modifier is made up by weight of following raw material:15 parts of polyamic acids, 3 parts of glass microballoons, 5 parts of stones Black alkene, 3 parts of bortz powders, 1 part of Silane coupling agent KH550,30 parts of DMF.Preparation method is:Polyamic acid is mixed with DMF, plus Heat is simultaneously stirred to polyamic acid and is completely dissolved, and is subsequently adding glass microballoon, silicon powder, bortz powder and Silane coupling agent KH550, It is uniformly mixed, is cooled to room temperature.
Embodiment 5:
The present embodiment is also added with 3 parts of abrasion resistance modifiers on the basis of the formula of embodiment 2.
The abrasion resistance modifier is made up by weight of following raw material:20 parts of polyamic acids, 5 parts of glass microballoons, 8 Part Graphene, 5 parts of bortz powders, 2 parts of Silane coupling agent KH550s, 50 parts of DMF.Preparation method is:By polyamic acid and DMF Mixing, heats and stirs to polyamic acid and be completely dissolved, and is subsequently adding glass microballoon, silicon powder, bortz powder and silane coupled Agent KH550, is uniformly mixed, and is cooled to room temperature.
Embodiment 6:
The present embodiment is also added with 4 parts of abrasion resistance modifiers on the basis of the formula of embodiment 3.
The abrasion resistance modifier is made up by weight of following raw material:18 parts of polyamic acids, 4 parts of glass microballoons, 6 parts of stones Black alkene, 4 parts of bortz powders, 1.5 parts of Silane coupling agent KH550s, 40 parts of DMF.Preparation method is:Polyamic acid is mixed with DMF, Heat and stir to polyamic acid and be completely dissolved, be subsequently adding glass microballoon, silicon powder, bortz powder and silane coupler KH550, is uniformly mixed, and is cooled to room temperature.
The preparation method step of embodiment 4-6 abrasive rubber is as follows:
1)First rubber is plasticated using banbury, plasticating temperature is 40-80 DEG C;
2)Then by step 1)It is rubber, zinc oxide, zinc powder, magnesinm methacrylate, hard acid fat, carbon black, magnesia after process, neat Polyester, coupling agent, accelerator, age resistor and abrasion resistance modifier, are then kneaded using banbury, melting temperature be 40 DEG C- 80℃;
3)Vulcanizing agent is added, is then turned refining again, finally vulcanized, curing temperature is 140-160 DEG C.
The abrasive rubber mechanics performance determining of the present invention presses national standard (GB/T528-1998, B/T529-1999, GB/ T531-1999) determine, Akron abrasion presses G B/T1689-1998 measure.After testing, abrasive rubber hardness of the invention (Shore A)80-90;Tensile strength 15.8-16.5MPa;Elongation at break 300%-320%;Akron abrasion 0.0052- 0.0086cm3/ 1.61km, 125-130 DEG C of the upper limit temperature of heat tolerance.
Embodiment described above is one kind preferably scheme of the present invention, not makees any pro forma to the present invention Limit, also have other variants and remodeling on the premise of without departing from the technical scheme described in claim.

Claims (10)

1. a kind of abrasive rubber, it is characterised in that the raw material of the abrasive rubber includes by weight following components:Rubber 100 parts, zinc oxide 1-2 parts, hard acid fat 3-10 parts, vulcanizing agent 1-3 parts, accelerator 2-5 parts, carbon black 50-100 parts, magnesia 3-10 parts, age resistor 1-3 parts, zinc powder 5-10 parts, magnesinm methacrylate 3-10 parts, oligomer ester 5-10 parts, coupling agent 1-3 Part.
2. a kind of abrasive rubber according to claim 1, it is characterised in that the raw material of the abrasive rubber is by weight Also include abrasion resistance modifier 3-5 parts.
3. a kind of abrasive rubber according to claim 2, it is characterised in that the abrasion resistance modifier by weight by with Lower raw material is made:15-20 part polyamic acids, 3-5 part glass microballoons, 5-8 part Graphenes, 3-5 part bortz powders, 1-2 part silane Coupling agent KH550,30-50 part DMF.
4. a kind of abrasive rubber according to claim 3, it is characterised in that the preparation method of the anti-wear agent is:Will be poly- Amic acid mixes with DMF, heats and stirs to polyamic acid and is completely dissolved, and is subsequently adding glass microballoon, silicon powder, bortz powder And Silane coupling agent KH550, it is uniformly mixed, it is cooled to room temperature.
5. a kind of abrasive rubber according to claim 1-4 any one, it is characterised in that the rubber is butyronitrile rubber One or two in glue, natural rubber.
6. a kind of abrasive rubber according to claim 1-4 any one, it is characterised in that the accelerator is tetramethyl Thiuram disulfides and 4, the mixture of 4 '-dithio morpholine.
7. a kind of abrasive rubber according to claim 1-4 any one, it is characterised in that the vulcanizing agent is peroxidating Diisopropylbenzene (DIPB).
8. a kind of abrasive rubber according to claim 1-4 any one, it is characterised in that the coupling agent is silane idol One or more in connection agent KH560, silane coupler KH570, silane coupler KH590.
9. the preparation method of abrasive rubber as claimed in claim 1, it is characterised in that step is as follows:
1)First rubber is plasticated using banbury, plasticating temperature is 40-80 DEG C;
2)Then by step 1)It is rubber, zinc oxide, zinc powder, magnesinm methacrylate, hard acid fat, carbon black, magnesia after process, neat Polyester, coupling agent, accelerator and age resistor, are then kneaded using banbury, and melting temperature is 40 DEG C -80 DEG C;
3)Vulcanizing agent is added, is then turned refining again, finally vulcanized, curing temperature is 140-160 DEG C.
10. the preparation method of abrasive rubber as claimed in claim 2, it is characterised in that step is as follows:
1)First rubber is plasticated using banbury, plasticating temperature is 40-80 DEG C;
2)Then by step 1)It is rubber, zinc oxide, zinc powder, magnesinm methacrylate, hard acid fat, carbon black, magnesia after process, neat Polyester, coupling agent, accelerator, age resistor and abrasion resistance modifier, are then kneaded using banbury, melting temperature be 40 DEG C- 80℃;
3)Vulcanizing agent is added, is then turned refining again, finally vulcanized, curing temperature is 140-160 DEG C.
CN201610953006.XA 2016-11-03 2016-11-03 Anti-wear rubber and preparation method thereof Pending CN106566028A (en)

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Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108250521A (en) * 2017-12-30 2018-07-06 张静 A kind of preparation method of wear-resisting type rubber soles
CN109369986A (en) * 2018-09-19 2019-02-22 南京金三力橡塑有限公司 A kind of orange peel shape rubber roller material and the method using its production orange peel shape rubber roller
CN110684250A (en) * 2019-11-19 2020-01-14 江苏创合橡塑有限公司 Ultrahigh-hardness nitrile rubber composition material and preparation method thereof
CN112538197A (en) * 2020-11-27 2021-03-23 无锡市德邦橡胶制业有限公司 Wear-resistant rubber floor mat and preparation method thereof
CN112980059A (en) * 2019-12-12 2021-06-18 徐工集团工程机械有限公司 Super-wear-resistant rubber, preparation method and crawler belt
CN116285039A (en) * 2023-03-22 2023-06-23 浙江华佑机械科技有限公司 Cam rubber rotor, preparation method thereof and cam pump using cam rubber rotor

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1187593A (en) * 1997-01-09 1998-07-15 扬中市中滩四氟密封件厂 Fibre rubber sealing material
CN1718623A (en) * 2004-07-09 2006-01-11 上海华化摩擦材料有限公司 Lining composite material and its preparation method
CN1896129A (en) * 2005-12-03 2007-01-17 河北九星橡塑制品有限公司 Abrasive synthetic rubber material and its production
CN101759887A (en) * 2010-01-29 2010-06-30 中实洛阳工程塑料有限公司 Method for preparing friction lining
CN101768296A (en) * 2008-12-31 2010-07-07 夏永宽 Special wear-resisting rubber composite
CN102924769A (en) * 2012-11-20 2013-02-13 上海神开石油化工装备股份有限公司 Rubber combination without frosting and turning white

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1187593A (en) * 1997-01-09 1998-07-15 扬中市中滩四氟密封件厂 Fibre rubber sealing material
CN1718623A (en) * 2004-07-09 2006-01-11 上海华化摩擦材料有限公司 Lining composite material and its preparation method
CN1896129A (en) * 2005-12-03 2007-01-17 河北九星橡塑制品有限公司 Abrasive synthetic rubber material and its production
CN101768296A (en) * 2008-12-31 2010-07-07 夏永宽 Special wear-resisting rubber composite
CN101759887A (en) * 2010-01-29 2010-06-30 中实洛阳工程塑料有限公司 Method for preparing friction lining
CN102924769A (en) * 2012-11-20 2013-02-13 上海神开石油化工装备股份有限公司 Rubber combination without frosting and turning white

Non-Patent Citations (4)

* Cited by examiner, † Cited by third party
Title
孙传尧主编: "《选矿工程师手册.第二册》", 31 March 2015, 冶金工业出版社 *
未标明作者: ""橡胶助硫化剂-甲基丙烯酸镁"", 《陕西化工》 *
翁国文 编著: "《实用橡胶配方技术》", 31 May 2008, 化学工业出版社 *
黄连经 主编: "《实用橡胶配方手册(下册)》", 31 December 1984 *

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108250521A (en) * 2017-12-30 2018-07-06 张静 A kind of preparation method of wear-resisting type rubber soles
CN109369986A (en) * 2018-09-19 2019-02-22 南京金三力橡塑有限公司 A kind of orange peel shape rubber roller material and the method using its production orange peel shape rubber roller
CN110684250A (en) * 2019-11-19 2020-01-14 江苏创合橡塑有限公司 Ultrahigh-hardness nitrile rubber composition material and preparation method thereof
CN112980059A (en) * 2019-12-12 2021-06-18 徐工集团工程机械有限公司 Super-wear-resistant rubber, preparation method and crawler belt
CN112538197A (en) * 2020-11-27 2021-03-23 无锡市德邦橡胶制业有限公司 Wear-resistant rubber floor mat and preparation method thereof
CN116285039A (en) * 2023-03-22 2023-06-23 浙江华佑机械科技有限公司 Cam rubber rotor, preparation method thereof and cam pump using cam rubber rotor
CN116285039B (en) * 2023-03-22 2024-05-07 浙江华佑机械科技有限公司 Cam rubber rotor, preparation method thereof and cam pump using cam rubber rotor

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