CN104531070A - Softwood particle blending and modified rubber based friction material as well as preparation method and using method thereof - Google Patents
Softwood particle blending and modified rubber based friction material as well as preparation method and using method thereof Download PDFInfo
- Publication number
- CN104531070A CN104531070A CN201410837982.XA CN201410837982A CN104531070A CN 104531070 A CN104531070 A CN 104531070A CN 201410837982 A CN201410837982 A CN 201410837982A CN 104531070 A CN104531070 A CN 104531070A
- Authority
- CN
- China
- Prior art keywords
- rubber
- cork
- friction material
- modified
- based friction
- 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.)
- Pending
Links
- 229920001971 elastomer Polymers 0.000 title claims abstract description 71
- 239000005060 rubber Substances 0.000 title claims abstract description 71
- 239000002783 friction material Substances 0.000 title claims abstract description 56
- 239000002245 particle Substances 0.000 title claims abstract description 41
- 238000000034 method Methods 0.000 title claims description 21
- 238000002360 preparation method Methods 0.000 title abstract description 8
- 238000002156 mixing Methods 0.000 title description 19
- 239000011122 softwood Substances 0.000 title 1
- 239000007799 cork Substances 0.000 claims abstract description 46
- 239000006087 Silane Coupling Agent Substances 0.000 claims abstract description 11
- 229920005989 resin Polymers 0.000 claims abstract description 11
- 239000011347 resin Substances 0.000 claims abstract description 11
- 239000012783 reinforcing fiber Substances 0.000 claims abstract description 10
- 239000000945 filler Substances 0.000 claims abstract description 9
- 239000003607 modifier Substances 0.000 claims abstract description 9
- 239000011230 binding agent Substances 0.000 claims abstract description 8
- 239000000654 additive Substances 0.000 claims abstract description 6
- 239000000203 mixture Substances 0.000 claims description 26
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 18
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 claims description 14
- 229920000459 Nitrile rubber Polymers 0.000 claims description 13
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 claims description 11
- 238000007731 hot pressing Methods 0.000 claims description 11
- 239000000843 powder Substances 0.000 claims description 10
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical class [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 claims description 8
- 229920006231 aramid fiber Polymers 0.000 claims description 8
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 claims description 8
- 239000000377 silicon dioxide Substances 0.000 claims description 8
- 235000012239 silicon dioxide Nutrition 0.000 claims description 8
- 244000226021 Anacardium occidentale Species 0.000 claims description 7
- 229920000049 Carbon (fiber) Polymers 0.000 claims description 7
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 7
- 239000004917 carbon fiber Substances 0.000 claims description 7
- 235000020226 cashew nut Nutrition 0.000 claims description 7
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims description 7
- 239000003921 oil Substances 0.000 claims description 7
- 239000011787 zinc oxide Substances 0.000 claims description 7
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 6
- 235000021355 Stearic acid Nutrition 0.000 claims description 6
- 239000003795 chemical substances by application Substances 0.000 claims description 6
- 239000010439 graphite Substances 0.000 claims description 6
- 229910002804 graphite Inorganic materials 0.000 claims description 6
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 claims description 6
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 claims description 6
- 239000008117 stearic acid Substances 0.000 claims description 6
- 239000011593 sulfur Substances 0.000 claims description 6
- 229910052717 sulfur Inorganic materials 0.000 claims description 6
- YHMYGUUIMTVXNW-UHFFFAOYSA-N 1,3-dihydrobenzimidazole-2-thione Chemical compound C1=CC=C2NC(S)=NC2=C1 YHMYGUUIMTVXNW-UHFFFAOYSA-N 0.000 claims description 5
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 5
- 238000010438 heat treatment Methods 0.000 claims description 5
- DEQZTKGFXNUBJL-UHFFFAOYSA-N n-(1,3-benzothiazol-2-ylsulfanyl)cyclohexanamine Chemical compound C1CCCCC1NSC1=NC2=CC=CC=C2S1 DEQZTKGFXNUBJL-UHFFFAOYSA-N 0.000 claims description 5
- 239000005995 Aluminium silicate Substances 0.000 claims description 4
- 235000012211 aluminium silicate Nutrition 0.000 claims description 4
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 claims description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 3
- 229920006282 Phenolic fiber Polymers 0.000 claims description 3
- 240000008289 Quercus suber Species 0.000 claims description 3
- 235000016977 Quercus suber Nutrition 0.000 claims description 3
- 239000012752 auxiliary agent Substances 0.000 claims description 3
- 229910052796 boron Inorganic materials 0.000 claims description 3
- -1 boron modified phenolic resin Chemical class 0.000 claims description 3
- 229920001973 fluoroelastomer Polymers 0.000 claims description 3
- 229920003048 styrene butadiene rubber Polymers 0.000 claims description 3
- 238000005520 cutting process Methods 0.000 claims description 2
- 239000003365 glass fiber Substances 0.000 claims description 2
- 229920001568 phenolic resin Polymers 0.000 claims description 2
- 239000005011 phenolic resin Substances 0.000 claims description 2
- 239000007787 solid Substances 0.000 claims description 2
- 238000005470 impregnation Methods 0.000 claims 1
- 230000004048 modification Effects 0.000 claims 1
- 238000012986 modification Methods 0.000 claims 1
- 239000000463 material Substances 0.000 abstract description 18
- 230000003068 static effect Effects 0.000 abstract description 12
- 239000004615 ingredient Substances 0.000 abstract 1
- 238000012360 testing method Methods 0.000 description 8
- 239000002994 raw material Substances 0.000 description 5
- 238000004898 kneading Methods 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 230000005540 biological transmission Effects 0.000 description 3
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 3
- 238000010074 rubber mixing Methods 0.000 description 3
- 229910000838 Al alloy Inorganic materials 0.000 description 2
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 2
- 239000010428 baryte Substances 0.000 description 2
- 229910052601 baryte Inorganic materials 0.000 description 2
- 230000009286 beneficial effect Effects 0.000 description 2
- 230000009977 dual effect Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000011737 fluorine Substances 0.000 description 2
- 229910052731 fluorine Inorganic materials 0.000 description 2
- 238000001878 scanning electron micrograph Methods 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 239000004113 Sepiolite Substances 0.000 description 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 229920000800 acrylic rubber Polymers 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 239000002008 calcined petroleum coke Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- UCNNJGDEJXIUCC-UHFFFAOYSA-L hydroxy(oxo)iron;iron Chemical compound [Fe].O[Fe]=O.O[Fe]=O UCNNJGDEJXIUCC-UHFFFAOYSA-L 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- HEQBUZNAOJCRSL-UHFFFAOYSA-N iron(ii) chromite Chemical compound [O-2].[O-2].[O-2].[Cr+3].[Fe+3] HEQBUZNAOJCRSL-UHFFFAOYSA-N 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 239000002557 mineral fiber Substances 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 150000001282 organosilanes Chemical class 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000012763 reinforcing filler Substances 0.000 description 1
- 239000012779 reinforcing material Substances 0.000 description 1
- 229910052624 sepiolite Inorganic materials 0.000 description 1
- 235000019355 sepiolite Nutrition 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 238000000859 sublimation Methods 0.000 description 1
- 230000008022 sublimation Effects 0.000 description 1
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
- Mechanical Operated Clutches (AREA)
Abstract
本发明涉及一种高摩擦系数低磨损率的软木颗粒共混改性橡胶基摩擦材料及其制备工艺。其成份为硅烷偶联剂改性软木颗粒20~35wt%,橡胶10~35wt%,有机树脂粘合剂4~8wt%,无机和有机增强纤维6~10wt%,摩擦性能调节剂和填料9~25wt%,橡胶助剂2~7wt%;该摩擦材料通过采用硅烷偶联剂改性软木颗粒与其他组分综合配比,使材料的动摩擦系数达到0.18~0.26,静摩擦系数达到0.27~0.35,同时材料的磨损率保持在4×10-8cm3/J以下。
The invention relates to a cork particle blended modified rubber-based friction material with high friction coefficient and low wear rate and a preparation process thereof. Its ingredients are 20-35wt% of silane coupling agent modified cork particles, 10-35wt% of rubber, 4-8wt% of organic resin binder, 6-10wt% of inorganic and organic reinforcing fibers, 9-9% of friction performance modifier and filler 25wt%, rubber additives 2-7wt%; the friction material uses silane coupling agent to modify the cork particles and other components in a comprehensive ratio, so that the dynamic friction coefficient of the material reaches 0.18-0.26, and the static friction coefficient reaches 0.27-0.35. The wear rate of the material is kept below 4×10 -8 cm 3 /J.
Description
技术领域technical field
本发明属于橡胶基摩擦材料及制备方法和使用方法,具体涉及一种软木颗粒共混改性橡胶基摩擦材料及制备方法,可用于摩托车离合器。The invention belongs to a rubber-based friction material and a preparation method and a use method thereof, in particular to a cork particle blended modified rubber-based friction material and a preparation method thereof, which can be used for motorcycle clutches.
背景技术Background technique
摩擦材料是一种应用于动力机械上,依靠摩擦性能作用来执行制动和传动功能的部件材料,它主要包括制动器衬片和离合器面片。摩擦材料广泛应用于摩托车等交通工具和机器设备的制动器和离合器等摩擦制动、传动装置中。Friction material is a component material that is applied to power machinery and relies on friction performance to perform braking and transmission functions. It mainly includes brake linings and clutch surfaces. Friction materials are widely used in friction braking and transmission devices such as brakes and clutches of vehicles such as motorcycles and mechanical equipment.
依据中华人民共和国国家标准GB/T13826-2008,摩托车离合器用橡胶基摩擦材料的动摩擦系数应该大于0.15,静摩擦系数应该不小于0.24。传统的橡胶基摩擦材料由增强纤维、橡胶与树脂粘结剂和摩擦性能调节剂三大组分构成,动摩擦系数0.1~0.2,静摩擦系数大于0.2,可满足湿式离合器的传动需要,但却存在几个问题,如摩擦材料磨损高、容易打滑、离合器换挡过程中发冲;同时由于摩托车离合器的压盘和中心套部件为铝合金成分,在传动制动过程中由于铝合金较钢材料硬度低,故该对偶件在工作过程中磨损较严重,从而影响摩托车离合器的使用寿命。According to the national standard GB/T13826-2008 of the People's Republic of China, the coefficient of dynamic friction of rubber-based friction materials for motorcycle clutches should be greater than 0.15, and the coefficient of static friction should not be less than 0.24. The traditional rubber-based friction material is composed of three major components: reinforcing fiber, rubber and resin binder, and friction modifier. There are two problems, such as high friction material wear, easy slipping, and rushing during clutch shifting; at the same time, because the pressure plate and center sleeve parts of the motorcycle clutch are made of aluminum alloy, the aluminum alloy is harder than steel during the transmission and braking process. Low, so the pair wears seriously during the working process, thus affecting the service life of the motorcycle clutch.
公开号为CN103205239A的中国专利公开了一种橡胶基摩擦材料及其制备方法,其配方含有质量百分比为15%~35%的丙烯酸酯橡胶;3%~15%的芳纶浆粕,或者碳纤维或者矿物纤维或是其中一种以上混合物;5%~25%的多功能摩擦颗粒;5%~20%的氧化铝,或者重晶石粉,或者铁黑,或者铬铁矿粉,或者鳞片石墨,或者煅烧石油焦炭或是其中一种以上混合物;2%~15%腰果壳油摩擦粉;2%~15%软木颗粒;2%~15%腰果壳油改性酚醛树脂;1%~7%的硫磺,或者促进剂DM,或者促进剂TMTD,或者氧化锌,或者硬脂酸或是其中一种以上混合物。该专利通过高速混料机将原料混合均匀,然后将混合物料投入密炼机在95℃~105℃下进行密炼并在开炼机进行炼胶混合,然后将预制体放入平板硫化机热压固化,最后进行热后处理得到橡胶基摩擦材料。该方法在将混合料投入密炼机时,由于温度过高造成橡胶组分提前硫化和交联,造成制品的硬度和弹性模量较高,在制动压力下与对偶表面的贴合性没有正硫化制品的贴合性好,摩擦表面的真实接触面积较小,材料的摩擦系数较低,其实施例中动摩擦系数为0.17~0.18,静摩擦系数为0.23~0.24,同时在摩擦过程中与对偶材料表面微凸体的接触很容易划伤材料表面,造成较高的磨损率,其实施例中材料的磨损率达到8×10-8m3/J。The Chinese patent with the publication number CN103205239A discloses a rubber-based friction material and its preparation method. Its formula contains 15% to 35% by mass of acrylic rubber; Mineral fiber or a mixture of more than one of them; 5% to 25% of multifunctional friction particles; 5% to 20% of alumina, or barite powder, or iron black, or chromite powder, or flake graphite, or Calcined petroleum coke or a mixture of one or more of them; 2% to 15% cashew nut shell oil friction powder; 2% to 15% cork particles; 2% to 15% cashew nut shell oil modified phenolic resin; 1% to 7% sulfur , or accelerator DM, or accelerator TMTD, or zinc oxide, or stearic acid, or a mixture of more than one of them. In this patent, the raw materials are mixed evenly by a high-speed mixer, and then the mixed materials are put into the internal mixer for internal mixing at 95°C to 105°C, and the rubber is mixed in the open mixer, and then the prefabricated body is put into a flat vulcanizing machine for heating. Press curing, and finally heat post-treatment to obtain rubber-based friction material. In this method, when the mixture is put into the internal mixer, the rubber component is vulcanized and cross-linked in advance due to the high temperature, resulting in high hardness and elastic modulus of the product, and the adhesion to the dual surface is not good under braking pressure. The fit of normal vulcanized products is good, the real contact area of the friction surface is small, and the friction coefficient of the material is low. In the examples, the dynamic friction coefficient is 0.17-0.18, and the static friction coefficient is 0.23-0.24. The contact of the asperities on the surface of the material can easily scratch the surface of the material, resulting in a high wear rate. In the example, the wear rate of the material reaches 8×10 -8 m 3 /J.
公开号为CN100572488C的中国专利公开了一种摩擦材料及其制备方法,其配方中纸基摩擦材料的主要组分重量百分比为:碳纤维或芳纶纤维20%~50%,棉绒浆15%~20%,石墨5%~10%,硅藻土和二氧化硅5%~10%,摩擦调整剂4%~20%,腰果壳油改性酚醛树脂15%~35%,着色剂0%~3%;橡胶软木摩擦材料的主要组分重量百分比为:丁腈橡胶、树脂及软木60%~80%,摩擦调整剂2%~10%,石墨5~10%,二氧化硅1%~5%,硅藻土2%~5%,氧化铝1%~5%,摩擦粉2%~5%,海泡石1%~5%。该专利其技术方案为一种摩擦材料包括衬片、纸基摩擦材料、橡胶软木摩擦材料。该专利通过分别制备纸基摩擦材料及橡胶软木型摩擦材料,然后将二者混合,在温度为200~300℃、压力3~10MPa、时间不超过1分钟条件下压制在衬片上,所述的纸基摩擦材料与橡胶软木摩擦材料的体积比为1:1~5,最后在140~180℃下固化2~6小时得到该摩擦材料。该方法需要分别制备纸基摩擦材料和橡胶软木型摩擦材料,工艺周期长,过程复杂,同时对两种材料的体积比控制要求精确,当纸基摩擦材料与橡胶软木摩擦材料的体积比大于1:5时不能实现发明的有益效果。按照GB/T13826-2008的标准要求,这类材料的动摩擦系数需大于0.15,静摩擦系数需不小于0.24,但是该专利的部分实施例所测量得到的动、静摩擦系数较低,不能满足上述标准要求,同时摩擦材料的磨损率较大,最高达到6×10-8cm3/J。The Chinese patent with the publication number CN100572488C discloses a friction material and its preparation method. The main components of the paper-based friction material in its formula are: 20% to 50% of carbon fiber or aramid fiber, and 15% to 15% of cotton wool pulp. 20%, graphite 5%~10%, diatomaceous earth and silicon dioxide 5%~10%, friction modifier 4%~20%, cashew nut shell oil modified phenolic resin 15%~35%, colorant 0%~ 3%; The main components of the rubber cork friction material are: 60% to 80% of nitrile rubber, resin and cork, 2% to 10% of friction modifier, 5 to 10% of graphite, 1% to 5% of silicon dioxide %, diatomite 2% to 5%, alumina 1% to 5%, friction powder 2% to 5%, sepiolite 1% to 5%. The technical proposal of the patent is that a friction material includes a lining, a paper-based friction material, and a rubber cork friction material. In this patent, paper-based friction material and rubber cork-type friction material are prepared separately, and then the two are mixed and pressed on the lining at a temperature of 200-300°C, a pressure of 3-10 MPa, and a time of no more than 1 minute. The volume ratio of the paper-based friction material to the rubber cork friction material is 1:1-5, and finally cured at 140-180° C. for 2-6 hours to obtain the friction material. This method needs to prepare paper-based friction material and rubber cork friction material separately, the process cycle is long, the process is complicated, and the volume ratio control of the two materials is required to be precise. When the volume ratio of paper-based friction material and rubber cork friction material is greater than 1 : In 5 o'clock, the beneficial effect of the invention cannot be realized. According to the standard requirements of GB/T13826-2008, the coefficient of dynamic friction of this type of material must be greater than 0.15, and the coefficient of static friction must not be less than 0.24, but the measured dynamic and static coefficients of some embodiments of the patent are low, which cannot meet the above standard requirements , and at the same time, the wear rate of the friction material is relatively high, up to 6×10 -8 cm 3 /J.
发明内容Contents of the invention
要解决的技术问题technical problem to be solved
为了避免现有技术的不足之处,本发明提出一种软木颗粒共混改性橡胶基摩擦材料及制备方法和使用方法,通过增大橡胶的质量百分含量,同时与其他组分相优化,克服现有橡胶基摩擦材料摩擦系数较低和材料磨损率较大的问题。In order to avoid the shortcomings of the prior art, the present invention proposes a cork particle blended modified rubber-based friction material and its preparation method and use method. By increasing the mass percentage of rubber and optimizing it with other components, The invention overcomes the problems of low friction coefficient and high material wear rate of existing rubber-based friction materials.
技术方案Technical solutions
一种软木颗粒共混改性橡胶基摩擦材料,其特征在于组份为:硅烷偶联剂改性软木颗粒20~35wt%,橡胶10~35wt%,有机树脂粘合剂4~8wt%,无机和有机增强纤维6~10wt%,摩擦性能调节剂和填料9~25wt%,橡胶助剂2~7wt%;组合物中各组分的重量百分比之和为100%。A cork particle blended modified rubber-based friction material, characterized in that the components are: silane coupling agent modified cork particle 20-35wt%, rubber 10-35wt%, organic resin binder 4-8wt%, inorganic 6-10% by weight of organic reinforcing fiber, 9-25% by weight of friction modifier and filler, and 2-7% by weight of rubber auxiliary agent; the sum of weight percentages of each component in the composition is 100%.
所述硅烷偶联剂改性软木颗粒采用栓皮栎树皮部分的木栓层制得,粒径为60目,采用硅烷偶联剂进行浸渍改性。The silane coupling agent-modified cork particles are prepared from the cork layer of the bark part of the cork oak, with a particle size of 60 mesh, and are impregnated and modified with the silane coupling agent.
所述橡胶为颗粒状固体,采用丁腈橡胶、氟橡胶或丁苯橡胶中的一种或一种以上混合物。The rubber is granular solid, and one or more mixtures of nitrile rubber, fluorine rubber or styrene-butadiene rubber are used.
所述有机树脂粘合剂为腰果壳油改性酚醛树脂、硼改性酚醛树脂或丁腈橡胶改性酚醛树脂中的一种或一种以上混合物。The organic resin binder is one or more mixtures of cashew nut shell oil modified phenolic resin, boron modified phenolic resin or nitrile rubber modified phenolic resin.
所述橡胶助剂为升华硫和硫化剂DCP混合、再加入促进剂DM、促进剂CZ、氧化锌、硬脂酸或防老剂MB中的三种或三种以上混合物。The rubber auxiliary agent is a mixture of sublimated sulfur and vulcanizing agent DCP, and then adding three or more mixtures of accelerator DM, accelerator CZ, zinc oxide, stearic acid or antioxidant MB.
所述无机和有机增强纤维是碳纤维与芳纶纤维、玻璃纤维、硫酸钙晶须或酚醛纤维中一种的混合物。The inorganic and organic reinforcing fibers are a mixture of carbon fiber and one of aramid fiber, glass fiber, calcium sulfate whisker or phenolic fiber.
所述的摩擦性能调节剂为氧化铝、二氧化硅、氧化锌、铁粉和鳞片石墨中的一种或一种以上混合物。The friction modifier is one or more mixtures of aluminum oxide, silicon dioxide, zinc oxide, iron powder and flake graphite.
所述填料黑胶粉、高岭土或硫酸钡。The filler is black rubber powder, kaolin or barium sulfate.
一种制备所述任一项软木颗粒共混改性橡胶基摩擦材料的方法,其特征在于步骤如下:A method for preparing any one of the cork particle blended modified rubber-based friction materials, characterized in that the steps are as follows:
步骤1:将硅烷偶联剂改性软木颗粒20%~35%、橡胶10%~35%、有机树脂粘合剂4%~8%、无机和有机增强纤维6%~10%、摩擦性能调节剂和填料9%~25%、橡胶助剂2%~7%进行混合,加入开放式炼胶机的辊轴间进行开练得到平板状预制体;所述开炼工艺参数为:温度为常温,时间5~7分钟;Step 1: 20% to 35% of cork particles modified by silane coupling agent, 10% to 35% of rubber, 4% to 8% of organic resin binder, 6% to 10% of inorganic and organic reinforcing fibers, friction performance adjustment 9% to 25% of additives and fillers, and 2% to 7% of rubber additives are mixed, and added between the rollers of an open rubber mixer to obtain a flat preform; , time 5-7 minutes;
步骤2:将平板状预制体在平板硫化机上进行热压固化,热压工艺参数为:温度160℃;压力5~10MPa。Step 2: The flat prefabricated body is cured by hot pressing on a flat vulcanizing machine, and the hot pressing process parameters are: temperature 160° C.; pressure 5-10 MPa.
一种采用所述摩擦材料制备摩托车离合器用衬板的方法,其特征在于:按照摩托车离合器用衬板的规格大小进行裁剪粘接,放入平板硫化机中进行热压成型,热压工艺参数为:温度160℃;压力5~7MPa;在进行后续热处理,后续热处理:室温升温至140℃保温1小时,再升温至155℃保温1小时,自然降至室温。A method for preparing a lining plate for a motorcycle clutch by using the friction material, which is characterized in that: cutting and bonding according to the specifications of the lining plate for a motorcycle clutch, putting it into a flat vulcanizing machine for hot-press forming, the hot-pressing process The parameters are: temperature 160°C; pressure 5-7MPa; follow-up heat treatment, follow-up heat treatment: the room temperature is raised to 140°C for 1 hour, then the temperature is raised to 155°C for 1 hour, and then it is naturally lowered to room temperature.
有益效果Beneficial effect
本发明提出的一种软木颗粒共混改性橡胶基摩擦材料及制备方法和使用方法,通过采用耐高温的丁腈橡胶、氟橡胶、高强度的芳纶纤维和碳纤维、硅烷偶联剂改性的软木颗粒,同时与多种复合成分的摩擦性能调节剂和填料相配合使用,得到了具有高摩擦系数和低磨损率的摩擦材料。所添加的软木颗粒由栓皮栎树皮部分的木栓层制得,具有独特的细胞构造使其具有质量轻、弹性好、柔软、耐磨等优良特性;硅烷偶联剂能与树脂、橡胶等有机材料和无机材料结合,是一种低分子有机硅烷,用它对软木颗粒进行改性,并添加到摩擦材料中,可以通过物理或化学反应使有机和无机组分之间形成分子桥,将二者结合起来,从而起到增强摩擦材料中树脂、增强纤维和填料之间的界面粘结,提高基体的强度和韧性,达到增大动、静摩擦系数,降低材料磨损率的效果;通过硅烷偶联剂的“桥联”作用在摩擦材料中形成了“高分子合金”的结构,提高了键能,在摩擦过程中材料受到外力时分散均衡应力,阻止材料裂纹扩展,从而达到增韧效果。硫酸钙晶须是一种新型增强材料,具有增强纤维和粉体填料的双重特殊作用,它具有耐热、耐磨损、耐腐蚀等优良特性,其成本比其他种类晶须要低,加入晶须可以改善摩擦材料的磨损性能。丁腈橡胶的耐热性优于其他橡胶,且其与酚醛树脂具有相似的溶解度参数,该技术方案采用粉末状橡胶可以简化混料工艺,达到缩短制备工艺周期的效果;同时采用开炼机与平板硫化机结合的生产工艺,简化了生产工艺,提高了对生产过程的可控性。当丁腈橡胶组分的质量百分含量为10%~35%时,橡胶基摩擦材料动摩擦系数由现有技术的0.17~0.19提高到0.23~0.26,静摩擦系数由现有技术的0.23~0.26提高到0.30~0.35,动摩擦系数与静摩擦系数的比值D/S可以达到0.66~0.86,磨损率由现有技术的7×10-8cm3/J降低为3×10-8cm3/J。The invention proposes a cork particle blended modified rubber-based friction material and its preparation method and use method, which are modified by using high-temperature-resistant nitrile rubber, fluororubber, high-strength aramid fiber and carbon fiber, and silane coupling agent The cork particles are used together with a variety of friction modifiers and fillers of composite components to obtain a friction material with a high friction coefficient and low wear rate. The added cork particles are made from the cork layer of the cork oak bark. It has a unique cell structure that makes it have excellent properties such as light weight, good elasticity, softness, and wear resistance; the silane coupling agent can be combined with resins, rubbers, etc. The combination of organic materials and inorganic materials is a low-molecular organosilane, which can be used to modify cork particles and add them to friction materials, which can form molecular bridges between organic and inorganic components through physical or chemical reactions. The combination of the two can enhance the interface bonding between the resin, reinforcing fiber and filler in the friction material, improve the strength and toughness of the matrix, increase the dynamic and static friction coefficient, and reduce the wear rate of the material; The "bridging" effect of the coupling agent forms a "polymer alloy" structure in the friction material, which improves the bond energy, disperses and balances the stress when the material is subjected to an external force during the friction process, and prevents the crack expansion of the material, thereby achieving the toughening effect. Calcium sulfate whisker is a new type of reinforcing material, which has dual special functions of reinforcing fiber and powder filler. It has excellent properties such as heat resistance, wear resistance, and corrosion resistance. Its cost is lower than other types of whiskers. Adding whiskers The wear performance of the friction material can be improved. The heat resistance of nitrile rubber is superior to other rubbers, and it has similar solubility parameters to phenolic resins. The technical solution uses powdered rubber to simplify the mixing process and shorten the production process cycle; The production process combined with the flat vulcanizing machine simplifies the production process and improves the controllability of the production process. When the mass percentage of the nitrile rubber component is 10% to 35%, the dynamic friction coefficient of the rubber-based friction material is increased from 0.17 to 0.19 in the prior art to 0.23 to 0.26, and the static friction coefficient is increased from 0.23 to 0.26 in the prior art The ratio D/S of the coefficient of dynamic friction to the coefficient of static friction can reach 0.66-0.86, and the wear rate is reduced from 7×10 -8 cm 3 /J in the prior art to 3×10 -8 cm 3 /J.
附图说明Description of drawings
图1:为实施例2制备出的软木颗粒共混改性橡胶基摩擦材料的表面扫描电镜图片。Figure 1: SEM images of the surface of the cork particle blended modified rubber-based friction material prepared in Example 2.
图2:为实施例4制备出的软木颗粒共混改性橡胶基摩擦材料的表面扫描电镜图片。Figure 2: SEM images of the surface of the cork particle blended modified rubber-based friction material prepared in Example 4.
具体实施方式Detailed ways
现结合实施例、附图对本发明作进一步描述:Now in conjunction with embodiment, accompanying drawing, the present invention will be further described:
实施例1:Example 1:
1)分别称取腰果壳油改性酚醛树脂4g、丁腈橡胶20g、氟橡胶2g、黑胶粉16g、芳纶纤维5g、碳纤维1g、软木颗粒30g、硫化剂DCP2g、升华硫1g、促进剂DM1g、促进剂CZ1g、氧化锌3g、氧化铝3g、重晶石5g、二氧化硅4g、铁粉3g。将以上原料放入小型混料机中分3次混合,每次混合时间不超过10秒,每次混合间隔3分钟至混合均匀;1) Weigh 4g of cashew nut shell oil modified phenolic resin, 20g of nitrile rubber, 2g of fluororubber, 16g of black rubber powder, 5g of aramid fiber, 1g of carbon fiber, 30g of cork particles, 2g of vulcanizing agent DCP, 1g of sublimated sulfur, and accelerator DM1g, accelerator CZ1g, zinc oxide 3g, aluminum oxide 3g, barite 5g, silicon dioxide 4g, iron powder 3g. Put the above raw materials into a small mixer and mix them in 3 times, each mixing time should not exceed 10 seconds, and each mixing interval should be 3 minutes until the mixing is uniform;
2)将混合料由少到多加入开放式炼胶机的辊轴间进行混炼,在常温下反复混炼5分钟,薄通20次以上得到均匀平板状预制体,开炼结束;2) Add the mixed material from less to more between the rollers of the open rubber mixer for mixing, and mix repeatedly at room temperature for 5 minutes, thin pass more than 20 times to obtain a uniform flat preform, and the kneading is over;
3)将步骤2)得到的预制体用游标卡尺测量厚度,在平板硫化机上在160℃、10MPa条件下进行热压固化;3) Measure the thickness of the preform obtained in step 2) with a vernier caliper, and perform hot-press curing on a flat vulcanizing machine at 160°C and 10MPa;
4)将步骤3)得到的胶皮按照摩托车离合器用衬板的规格大小进行裁剪粘接,放入平板硫化机中进行热压成型;4) The rubber obtained in step 3) is cut and bonded according to the size of the liner for the motorcycle clutch, and put into a flat vulcanizer for hot pressing;
5)将步骤4)得到的产品于140℃条件下热处理一小时,经半小时升温至155℃热处理一小时,得到软木颗粒共混改性橡胶基摩擦材料。5) The product obtained in step 4) was heat-treated at 140° C. for one hour, then raised to 155° C. for half an hour and heat-treated for one hour to obtain a cork particle blended modified rubber-based friction material.
采用QM1000-ⅡB型湿式摩擦性能试验机,按照GB/T13826-2008标准进行测试,得到动摩擦系数0.20~0.24,静摩擦系数0.34~0.35,磨损率小于3×10-8cm3/J。The QM1000-ⅡB wet friction performance testing machine was used to test according to the GB/T13826-2008 standard, and the dynamic friction coefficient was 0.20-0.24, the static friction coefficient was 0.34-0.35, and the wear rate was less than 3×10 -8 cm 3 /J.
实施例2:Example 2:
1)分别称取丁腈橡胶改性酚醛树脂4g、丁腈橡胶25g、氟橡胶3g、黑胶粉12g、芳纶纤维5g、酚醛纤维1g、软木颗粒28g、硫化剂DCP2.5g、升华硫1.5g、促进剂CZ1g、硬脂酸1g、防老剂MB1g、氧化铝2g、高岭土5g、硫酸钡4g、二氧化硅4g。将以上原料放入小型混料机中混合3次,每次混合时间不超过10秒,混合间隔3分钟至混合均匀;1) Weigh 4g of nitrile rubber modified phenolic resin, 25g of nitrile rubber, 3g of fluorine rubber, 12g of black rubber powder, 5g of aramid fiber, 1g of phenolic fiber, 28g of cork particles, 2.5g of vulcanizing agent DCP, and 1.5g of sublimated sulfur g, accelerator CZ 1g, stearic acid 1g, antioxidant MB 1g, alumina 2g, kaolin 5g, barium sulfate 4g, silicon dioxide 4g. Put the above raw materials into a small mixer and mix 3 times, each mixing time is no more than 10 seconds, and the mixing interval is 3 minutes until the mixing is uniform;
2)将混合料由少到多渐次加入开放式炼胶机的辊轴间进行混炼,在常温下反复混炼6分钟,薄通20次以上得到均匀平板状预制体,开炼结束;2) Gradually add the mixed material between the rollers of the open rubber mixing machine from less to more for mixing, and mix repeatedly at room temperature for 6 minutes, thin pass more than 20 times to obtain a uniform flat preform, and the kneading is over;
3)将步骤2)得到的预制体用游标卡尺测量厚度,在平板硫化机上160℃、10MPa条件下进行热压固化;3) Measure the thickness of the preform obtained in step 2) with a vernier caliper, and perform hot-press curing on a flat vulcanizing machine at 160°C and 10MPa;
4)将步骤3)得到的胶皮按照摩托车离合器用衬板的规格大小进行裁剪粘接,放入平板硫化机上进行热压成型;4) The rubber obtained in step 3) is cut and bonded according to the specifications of the liner for the motorcycle clutch, and put into a flat vulcanizing machine for hot pressing;
5)将步骤4)得到的产品在140℃条件下热处理一小时,经半小时升温至155℃热处理一小时,得到软木颗粒共混改性橡胶基摩擦材料。5) The product obtained in step 4) was heat-treated at 140° C. for one hour, then raised to 155° C. for half an hour and heat-treated for one hour to obtain a cork particle blended modified rubber-based friction material.
采用QM1000-ⅡB型湿式摩擦性能试验机,按照GB/T13826-2008标准进行测试,得到动摩擦系数0.19~0.23,静摩擦系数0.29~0.31,磨损率小于2×10-8cm3/J。The QM1000-ⅡB wet friction performance testing machine was used to test according to the GB/T13826-2008 standard, and the dynamic friction coefficient was 0.19-0.23, the static friction coefficient was 0.29-0.31, and the wear rate was less than 2×10 -8 cm 3 /J.
实施例3:Example 3:
1)分别称取腰果壳油改性酚醛树脂4g、丁腈橡胶30g、丁苯橡胶3g、黑胶粉9g、芳纶纤维5g、碳纤维1g、硫酸钙晶须2g、软木颗粒27g、硫化剂DCP3g、升华硫1g、硬脂酸1g、防老剂MB1g、促进剂CZ1g、氧化锌2g、二氧化硅3g、鳞片石墨3g、硫酸钡3g、氧化铝1g。将以上原料放入小型混料机中混合3次,每次混合时间不超过10秒,混合间隔3分钟至混合均匀;1) Weigh 4g of cashew nut shell oil modified phenolic resin, 30g of nitrile rubber, 3g of styrene-butadiene rubber, 9g of black rubber powder, 5g of aramid fiber, 1g of carbon fiber, 2g of calcium sulfate whisker, 27g of cork particles, and 3g of vulcanizing agent DCP , sublimed sulfur 1g, stearic acid 1g, antioxidant MB 1g, accelerator CZ 1g, zinc oxide 2g, silicon dioxide 3g, flake graphite 3g, barium sulfate 3g, aluminum oxide 1g. Put the above raw materials into a small mixer and mix 3 times, the mixing time should not exceed 10 seconds each time, and the mixing interval should be 3 minutes until the mixing is uniform;
2)将混合料由少到多渐次加入开放式炼胶机的辊轴间进行混炼,在常温下反复混炼5分钟,薄通20次以上得到均匀平板状预制体,开炼结束;2) Gradually add the mixed material between the rollers of the open rubber mixing machine from small to large for mixing, and mix repeatedly at room temperature for 5 minutes, thin pass more than 20 times to obtain a uniform flat preform, and the kneading is over;
3)将步骤2)得到的预制体用游标卡尺测量厚度在平板硫化机上160℃、10MPa条件下进行热压固化;3) Measure the thickness of the preform obtained in step 2) with a vernier caliper and perform hot-press curing on a flat vulcanizing machine at 160°C and 10MPa;
4)将步骤3)得到的胶皮按照摩托车离合器用衬板的规格大小进行裁剪粘接,放入平板硫化机上进行热压成型;4) The rubber obtained in step 3) is cut and bonded according to the specifications of the liner for the motorcycle clutch, and put into a flat vulcanizing machine for hot pressing;
5)将步骤4)得到的产品在140℃条件下热处理一小时,经半小时升温至155℃热处理一小时,得到软木颗粒共混改性橡胶基摩擦材料。5) The product obtained in step 4) was heat-treated at 140° C. for one hour, then raised to 155° C. for half an hour and heat-treated for one hour to obtain a cork particle blended modified rubber-based friction material.
采用QM1000-ⅡB型湿式摩擦性能试验机,按照GB/T13826-2008标准进行测试,得到动摩擦系数0.20~0.25,静摩擦系数0.35~0.36,磨损率小于3×10-8cm3/J。The QM1000-ⅡB wet friction performance testing machine was used to test according to the GB/T13826-2008 standard, and the dynamic friction coefficient was 0.20-0.25, the static friction coefficient was 0.35-0.36, and the wear rate was less than 3×10 -8 cm 3 /J.
实施例4:Example 4:
1)分别称取硼改性酚醛树脂4g、丁腈橡胶35g、黑胶粉9g、芳纶纤维5g、碳纤维1g、软木颗粒28.5g、硫化剂DCP3.5g、促进剂CZ1g、促进剂DM1g、升华硫1.5g、防老剂MB1g、硬脂酸0.5g、氧化铝1g、高岭土2g、重晶石3g、二氧化硅3g。将以上原料放入小型混料机中混合3次,每次混合时间不超过10秒,混合间隔3分钟至混合均匀;1) Weigh 4g of boron modified phenolic resin, 35g of nitrile rubber, 9g of black rubber powder, 5g of aramid fiber, 1g of carbon fiber, 28.5g of cork particles, 3.5g of vulcanizing agent DCP, 1g of accelerator CZ, 1g of accelerator DM, sublimation Sulfur 1.5g, antioxidant MB 1g, stearic acid 0.5g, alumina 1g, kaolin 2g, barite 3g, silicon dioxide 3g. Put the above raw materials into a small mixer and mix 3 times, the mixing time should not exceed 10 seconds each time, and the mixing interval should be 3 minutes until the mixing is uniform;
2)将混合料由少到多渐次加入开放式炼胶机的辊轴间进行混炼,在常温下反复混炼7分钟,薄通20次以上得到均匀平板状预制体,开炼结束;2) Gradually add the mixed material between the rollers of the open rubber mixing machine from less to more for mixing, and mix repeatedly at room temperature for 7 minutes, thin pass more than 20 times to obtain a uniform flat preform, and the kneading is over;
3)将步骤2)得到的预制体用游标卡尺测量厚度,在平板硫化机上160℃、10MPa条件下进行热压固化;3) Measure the thickness of the preform obtained in step 2) with a vernier caliper, and perform hot-press curing on a flat vulcanizing machine at 160°C and 10MPa;
4)将步骤3)得到的胶皮按照摩托车离合器用衬板的规格大小进行裁剪粘接,放入平板硫化机上进行热压成型;4) The rubber obtained in step 3) is cut and bonded according to the specifications of the liner for the motorcycle clutch, and put into a flat vulcanizing machine for hot pressing;
5)将步骤4)得到的产品在140℃条件下热处理一小时,经半小时升温至155℃热处理一小时,得到软木颗粒共混改性橡胶基摩擦材料。5) The product obtained in step 4) was heat-treated at 140° C. for one hour, then raised to 155° C. for half an hour and heat-treated for one hour to obtain a cork particle blended modified rubber-based friction material.
采用QM1000-ⅡB型湿式摩擦性能试验机,按照GB/T13826-2008标准进行测试,得到动摩擦系数0.18~0.26,静摩擦系数0.29~0.33,磨损率小于3×10-8cm3/J。The QM1000-ⅡB wet friction performance testing machine was used to test according to the GB/T13826-2008 standard, and the dynamic friction coefficient was 0.18-0.26, the static friction coefficient was 0.29-0.33, and the wear rate was less than 3×10 -8 cm 3 /J.
Claims (10)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201410837982.XA CN104531070A (en) | 2014-12-29 | 2014-12-29 | Softwood particle blending and modified rubber based friction material as well as preparation method and using method thereof |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201410837982.XA CN104531070A (en) | 2014-12-29 | 2014-12-29 | Softwood particle blending and modified rubber based friction material as well as preparation method and using method thereof |
Publications (1)
Publication Number | Publication Date |
---|---|
CN104531070A true CN104531070A (en) | 2015-04-22 |
Family
ID=52846709
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201410837982.XA Pending CN104531070A (en) | 2014-12-29 | 2014-12-29 | Softwood particle blending and modified rubber based friction material as well as preparation method and using method thereof |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN104531070A (en) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN105385146A (en) * | 2015-12-22 | 2016-03-09 | 合肥仲农生物科技有限公司 | Cork rubber compound |
CN107675313A (en) * | 2017-10-20 | 2018-02-09 | 来安县隆华摩擦材料有限公司 | A kind of preparation method of clutch surface without the expanded complex yarn of asbestos fibre |
CN107906148A (en) * | 2017-11-23 | 2018-04-13 | 铜陵市东方矿冶机械有限责任公司 | HIgh strength drying friction plate and preparation method thereof |
CN108559252A (en) * | 2017-12-19 | 2018-09-21 | 翟琳 | A kind of preparation method of railroad track resilient sleeper-bearing |
CN109235119A (en) * | 2018-09-27 | 2019-01-18 | 佛山九陌科技信息咨询有限公司 | A kind of preparation method of enhanced paper friction material |
CN112458789A (en) * | 2020-11-27 | 2021-03-09 | 西北工业大学 | Rubber resin double-matrix wet-type friction material and preparation method thereof |
CN115093720A (en) * | 2022-06-08 | 2022-09-23 | 杭州汉乐科新材料科技有限公司 | Motorcycle clutch friction plate containing walnut shell powder and preparation method thereof |
CN115572455A (en) * | 2022-11-04 | 2023-01-06 | 贵州省材料产业技术研究院 | Phosphogypsum whisker/fiber reinforced composite material and preparation method thereof |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101429297A (en) * | 2008-12-17 | 2009-05-13 | 黄山奔马集团有限公司 | Friction plate material and its use method |
CN103205239A (en) * | 2013-04-15 | 2013-07-17 | 杭州安凯机械有限公司 | Rubber base friction material and production method thereof |
-
2014
- 2014-12-29 CN CN201410837982.XA patent/CN104531070A/en active Pending
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101429297A (en) * | 2008-12-17 | 2009-05-13 | 黄山奔马集团有限公司 | Friction plate material and its use method |
CN103205239A (en) * | 2013-04-15 | 2013-07-17 | 杭州安凯机械有限公司 | Rubber base friction material and production method thereof |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN105385146A (en) * | 2015-12-22 | 2016-03-09 | 合肥仲农生物科技有限公司 | Cork rubber compound |
CN107675313A (en) * | 2017-10-20 | 2018-02-09 | 来安县隆华摩擦材料有限公司 | A kind of preparation method of clutch surface without the expanded complex yarn of asbestos fibre |
CN107675313B (en) * | 2017-10-20 | 2019-05-10 | 来安县隆华摩擦材料有限公司 | A kind of preparation method of the no asbestos fibre extruding complex yarn of clutch surface |
CN107906148A (en) * | 2017-11-23 | 2018-04-13 | 铜陵市东方矿冶机械有限责任公司 | HIgh strength drying friction plate and preparation method thereof |
CN108559252A (en) * | 2017-12-19 | 2018-09-21 | 翟琳 | A kind of preparation method of railroad track resilient sleeper-bearing |
CN109235119A (en) * | 2018-09-27 | 2019-01-18 | 佛山九陌科技信息咨询有限公司 | A kind of preparation method of enhanced paper friction material |
CN112458789A (en) * | 2020-11-27 | 2021-03-09 | 西北工业大学 | Rubber resin double-matrix wet-type friction material and preparation method thereof |
CN115093720A (en) * | 2022-06-08 | 2022-09-23 | 杭州汉乐科新材料科技有限公司 | Motorcycle clutch friction plate containing walnut shell powder and preparation method thereof |
CN115093720B (en) * | 2022-06-08 | 2023-09-08 | 杭州汉乐科新材料科技有限公司 | Motorcycle clutch friction plate containing walnut shell powder and preparation method thereof |
CN115572455A (en) * | 2022-11-04 | 2023-01-06 | 贵州省材料产业技术研究院 | Phosphogypsum whisker/fiber reinforced composite material and preparation method thereof |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN104531070A (en) | Softwood particle blending and modified rubber based friction material as well as preparation method and using method thereof | |
CN105114498B (en) | PPTA composite fibre dry clutch dough sheet and preparation method thereof | |
CN108728041B (en) | A kind of low-metal environment-friendly friction material for automobile brake pads and preparation method thereof | |
CN101077912B (en) | Asbestos-free non-metal friction material and preparation method thereof | |
CN100516122C (en) | A method for preparing friction material by wet mixing | |
CN101186710B (en) | Potassium hexatitanate/sodium hexatitanate whisker composite ceramic friction material and preparation method thereof | |
KR101966446B1 (en) | Manufacturing method for a friction material | |
CN101813147B (en) | Brake pad and preparation method thereof | |
CN104109342B (en) | A kind of low noise, heat resistanceheat resistant decline resin-matrix friction material | |
CN103992769B (en) | A kind of car is used without copper high-performance environment protection type friction materials and preparation method | |
CN102277133B (en) | High temperature-resistant composite ceramic friction material | |
CN102093841A (en) | Double-adhesive friction material | |
EP3085985B1 (en) | Composition for friction material | |
CN101555399A (en) | Novel brake pad material of truck | |
CN103409109A (en) | Friction material used in disc brake | |
CN105038101B (en) | A kind of cellulose reinforced anti-stick disc anti-whistling wear-resistant brake material and preparation method thereof | |
CN101759958A (en) | Enhanced ceramic friction material and preparation method thereof | |
CN101514251B (en) | Vehicle braking composite material reinforced by confusion of natural fiber and crystal whisker and preparing method thereof | |
CN105402292B (en) | A kind of automotive brake pads and preparation method thereof | |
CN113124076A (en) | Low-resin-based aramid pulp wear-resistant disc brake pad and preparation method thereof | |
JP6066739B2 (en) | Friction material and manufacturing method thereof | |
CN106907414A (en) | Automotive disc brake non-metallic friction materials and its preparation method and application | |
CN101671465A (en) | Preparation method of ethoxyline resin/polytetrafluoroethylene composite material | |
CN115975336A (en) | A kind of low-noise friction material and its preparation method and application | |
CN101576136A (en) | Non-metal ceramic-based automobile brake sheet and preparing method thereof |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
WD01 | Invention patent application deemed withdrawn after publication |
Application publication date: 20150422 |
|
WD01 | Invention patent application deemed withdrawn after publication |