CN111333982B - A kind of polytetrafluoroethylene friction material and its preparation method and application - Google Patents
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Abstract
本发明提供了一种聚四氟乙烯摩擦材料及其制备方法和应用,涉及摩擦材料技术领域。本发明的聚四氟乙烯摩擦材料包括以下质量份的制备原料:聚四氟乙烯65~80份、纳米氮化硼1~5份、二硫化钼5~15份、纳米氧化锆1~5份、碳量子点1~5份、片层纳米Ti3C2 1~5份。本发明添加片层纳米Ti3C2,片层纳米Ti3C2独特的二维层状结构使其具有优异的摩擦学特性,配合其他组分,得到的聚四氟乙烯摩擦材料可显著改善大型超声电机的启停特性。
The invention provides a polytetrafluoroethylene friction material, a preparation method and application thereof, and relates to the technical field of friction materials. The polytetrafluoroethylene friction material of the present invention includes the following raw materials in parts by mass: 65-80 parts of polytetrafluoroethylene, 1-5 parts of nano-boron nitride, 5-15 parts of molybdenum disulfide, and 1-5 parts of nano-zirconia , 1-5 parts of carbon quantum dots, and 1-5 parts of lamellar nano-Ti 3 C 2 . The invention adds lamella nano Ti 3 C 2 , and the unique two-dimensional layered structure of lamella nano Ti 3 C 2 makes it have excellent tribological properties, and with other components, the obtained PTFE friction material can be significantly improved Start-stop characteristics of large ultrasonic motors.
Description
技术领域technical field
本发明涉及摩擦材料技术领域,尤其涉及一种聚四氟乙烯摩擦材料及其制备方法和应用。The invention relates to the technical field of friction materials, in particular to a polytetrafluoroethylene friction material and a preparation method and application thereof.
背景技术Background technique
超声电机是一种新型精密驱动微特电机,通过能量转换和运动传递,对负载实施力或力矩作用,以达到控制负载精确运动/定位的目的。作为精密驱动部件,超声电机广泛应用于航空航天、武器装备及机器人等领域,推动装备向高精度、高效率、高可靠性、智能化和轻量化方向发展,其对国家科技影响力和国防威慑力具有重要影响。Ultrasonic motor is a new type of precision-driven micro-motor. Through energy conversion and motion transmission, it applies force or torque to the load to achieve the purpose of controlling the precise movement/positioning of the load. As a precision drive component, ultrasonic motors are widely used in aerospace, weapon equipment and robotics fields, promoting the development of equipment in the direction of high precision, high efficiency, high reliability, intelligence and light weight, and its influence on national science and technology and national defense deterrence power has an important impact.
大量研究工作者发现超声电机使用时会出现无法正常启动的问题,特别是放置一段时间后,这一问题严重阻碍超声电机的可靠性,因此其在航空航天、武器装备等领域的发展受到了严重的制约。上述问题在大型超声电机(直径为150mm)中更加明显。影响超声电机启停特性的一个重要问题就是摩擦材料。传统改善摩擦材料的填料例如碳纤维、芳纶纤维、硅石灰等功能单一,对超声电机的启停性改善效果不佳。A large number of researchers have found that the ultrasonic motor cannot be started normally when it is used, especially after being placed for a period of time, this problem seriously hinders the reliability of the ultrasonic motor, so its development in aerospace, weaponry and other fields has been seriously affected. constraints. The above problems are more pronounced in large ultrasonic motors (150mm in diameter). An important issue that affects the start-stop characteristics of ultrasonic motors is the friction material. The traditional fillers for improving friction materials, such as carbon fiber, aramid fiber, and silica lime, have a single function, and the effect of improving the start-stop performance of the ultrasonic motor is not good.
发明内容SUMMARY OF THE INVENTION
本发明的目的在于提供一种聚四氟乙烯摩擦材料及其制备方法和应用,本发明的聚四氟乙烯摩擦材料能够显著改善大型超声电机的启停特性。The purpose of the present invention is to provide a polytetrafluoroethylene friction material and a preparation method and application thereof. The polytetrafluoroethylene friction material of the present invention can significantly improve the start-stop characteristics of large ultrasonic motors.
为了实现上述发明目的,本发明提供以下技术方案:In order to achieve the above-mentioned purpose of the invention, the present invention provides the following technical solutions:
本发明提供了一种聚四氟乙烯摩擦材料,包括以下质量份的制备原料:聚四氟乙烯65~80份、纳米氮化硼1~5份、二硫化钼5~15份、纳米氧化锆1~5份、碳量子点1~5份、片层纳米Ti3C2 1~5份。The invention provides a polytetrafluoroethylene friction material, comprising the following raw materials in parts by mass: 65-80 parts of polytetrafluoroethylene, 1-5 parts of nano-boron nitride, 5-15 parts of molybdenum disulfide, and nano-zirconia 1 to 5 parts, 1 to 5 parts of carbon quantum dots, and 1 to 5 parts of lamellar nano-Ti 3 C 2 .
优选的,制备原料包括聚四氟乙烯70~80份、纳米氮化硼2~5份、二硫化钼7~15份、纳米氧化锆3~5份、碳量子点2~5份、片层纳米Ti3C2 2~4份。Preferably, the preparation raw materials include 70-80 parts of polytetrafluoroethylene, 2-5 parts of nano-boron nitride, 7-15 parts of molybdenum disulfide, 3-5 parts of nano-zirconia, 2-5 parts of carbon quantum dots, lamellae 2-4 parts of nano-Ti 3 C 2 .
优选的,所述片层纳米Ti3C2的单层厚度为80~100nm。Preferably, the single-layer thickness of the lamellar nano-Ti 3 C 2 is 80-100 nm.
优选的,所述聚四氟乙烯的粒径为65~75μm;所述纳米氮化硼的片径为0.3~2nm;所述二硫化钼的片径为15~25μm;所述纳米氧化锆的粒径为20~40nm;所述碳量子点的粒径为3~5nm。Preferably, the particle size of the polytetrafluoroethylene is 65-75 μm; the sheet diameter of the nano-boron nitride is 0.3-2 nm; the sheet diameter of the molybdenum disulfide is 15-25 μm; The particle size is 20-40 nm; the particle size of the carbon quantum dots is 3-5 nm.
本发明提供了上述方案所述聚四氟乙烯摩擦材料的制备方法,包括以下步骤:The present invention provides the preparation method of the polytetrafluoroethylene friction material described in the above scheme, comprising the following steps:
将各制备原料进行混合,对得到的混合料依次进行压制和烧结,得到聚四氟乙烯摩擦材料。The preparation raw materials are mixed, and the obtained mixed materials are sequentially pressed and sintered to obtain a polytetrafluoroethylene friction material.
优选的,所述压制的压力为70~100MPa,时间为3~5min。Preferably, the pressing pressure is 70-100 MPa, and the time is 3-5 min.
优选的,所述烧结的温度为365~375℃,保温时间为90~150min。Preferably, the sintering temperature is 365-375° C., and the holding time is 90-150 min.
优选的,所述混合的过程为:将各制备原料分散到乙醇或丙酮中,干燥后得到混合料。Preferably, the mixing process is as follows: each preparation raw material is dispersed in ethanol or acetone, and the mixture is obtained after drying.
本发明提供了上述方案所述聚四氟乙烯摩擦材料或上述方案所述制备方法制备得到的聚四氟乙烯摩擦材料在超声电机中的应用。The present invention provides the application of the polytetrafluoroethylene friction material in the above scheme or the polytetrafluoroethylene friction material prepared by the preparation method in the above scheme in an ultrasonic motor.
优选的,所述超声电机的直径在150mm以上。Preferably, the diameter of the ultrasonic motor is more than 150 mm.
本发明提供了一种聚四氟乙烯摩擦材料,包括以下质量份的制备原料:聚四氟乙烯65~80份、纳米氮化硼1~5份、二硫化钼5~15份、纳米氧化锆1~5份、碳量子点1~5份、片层纳米Ti3C2 1~5份。本发明添加片层纳米Ti3C2,片层纳米Ti3C2独特的二维层状结构使其具有优异的摩擦学特性,配合其他组分,得到的聚四氟乙烯摩擦材料可显著改善大型超声电机的启停特性。The invention provides a polytetrafluoroethylene friction material, comprising the following raw materials in parts by mass: 65-80 parts of polytetrafluoroethylene, 1-5 parts of nano-boron nitride, 5-15 parts of molybdenum disulfide, and nano-zirconia 1 to 5 parts, 1 to 5 parts of carbon quantum dots, and 1 to 5 parts of lamellar nano-Ti 3 C 2 . The invention adds lamella nano Ti 3 C 2 , and the unique two-dimensional layered structure of lamella nano Ti 3 C 2 makes it have excellent tribological properties, and with other components, the obtained PTFE friction material can be significantly improved Start-stop characteristics of large ultrasonic motors.
附图说明Description of drawings
图1为本发明所用片层纳米Ti3C2的扫描电镜照片。Fig. 1 is the scanning electron microscope photograph of lamella nano Ti 3 C 2 used in the present invention.
具体实施方式Detailed ways
本发明提供了一种聚四氟乙烯摩擦材料,包括以下质量份的制备原料:聚四氟乙烯65~80份、纳米氮化硼1~5份、二硫化钼5~15份、纳米氧化锆1~5份、碳量子点1~5份、片层纳米Ti3C2 1~5份。The invention provides a polytetrafluoroethylene friction material, comprising the following raw materials in parts by mass: 65-80 parts of polytetrafluoroethylene, 1-5 parts of nano-boron nitride, 5-15 parts of molybdenum disulfide, and nano-zirconia 1 to 5 parts, 1 to 5 parts of carbon quantum dots, and 1 to 5 parts of lamellar nano-Ti 3 C 2 .
在本发明中,未经特殊说明,所用原料均为本领域熟知的市售商品。In the present invention, without special instructions, the raw materials used are all commercially available commodities well known in the art.
以质量份计,本发明提供的聚四氟乙烯摩擦材料的制备原料包括聚四氟乙烯65~80份,优选为70~80份,更优选为70~75份。在本发明中,所述聚四氟乙烯的粒径优选为65~75μm,更优选为68~73μm。在本发明中,所述聚四氟乙烯优选购自山东济南三爱富氟化工有限责任公司。In parts by mass, the raw materials for the preparation of the polytetrafluoroethylene friction material provided by the present invention include 65-80 parts of polytetrafluoroethylene, preferably 70-80 parts, and more preferably 70-75 parts. In the present invention, the particle size of the polytetrafluoroethylene is preferably 65 to 75 μm, and more preferably 68 to 73 μm. In the present invention, the polytetrafluoroethylene is preferably purchased from Shandong Jinan Sanai Fu Fluorine Chemical Co., Ltd.
以所述聚四氟乙烯的质量份为基准,本发明提供的聚四氟乙烯摩擦材料的制备原料包括纳米氮化硼1~5份,优选为2~5份,更优选为3~5份。在本发明中,所述纳米氮化硼的片径优选为0.3~2nm,更优选为1~1.5nm。在本发明中,所述纳米氮化硼的作用是提高聚四氟乙烯摩擦材料的耐磨性。Based on the mass parts of the polytetrafluoroethylene, the preparation raw materials of the polytetrafluoroethylene friction material provided by the present invention include 1-5 parts of nano-boron nitride, preferably 2-5 parts, more preferably 3-5 parts . In the present invention, the sheet diameter of the nano-boron nitride is preferably 0.3-2 nm, more preferably 1-1.5 nm. In the present invention, the role of the nano-boron nitride is to improve the wear resistance of the PTFE friction material.
以所述聚四氟乙烯的质量份为基准,本发明提供的聚四氟乙烯摩擦材料的制备原料包括二硫化钼5~15份,优选为7~15份,更优选为10~15份。在本发明中,所述二硫化钼的片径优选为15~25μm,更优选为18~23μm。本发明优选采用北京德科岛金科技有限公司的二硫化钼。在本发明中,所述二硫化钼的作用是提高聚四氟乙烯摩擦材料的耐磨性和摩擦系数的稳定性。Based on the mass parts of the polytetrafluoroethylene, the preparation raw materials of the polytetrafluoroethylene friction material provided by the present invention include 5-15 parts of molybdenum disulfide, preferably 7-15 parts, more preferably 10-15 parts. In the present invention, the sheet diameter of the molybdenum disulfide is preferably 15 to 25 μm, and more preferably 18 to 23 μm. The present invention preferably adopts molybdenum disulfide from Beijing Dekedao Gold Technology Co., Ltd. In the present invention, the function of the molybdenum disulfide is to improve the wear resistance and the stability of the friction coefficient of the PTFE friction material.
以所述聚四氟乙烯的质量份为基准,本发明提供的聚四氟乙烯摩擦材料的制备原料包括纳米氧化锆1~5份,优选为3~5份,更优选为4~5份。在本发明中,所述纳米氧化锆的粒径优选为20~40nm,更优选为25~35nm。在本发明中,所述纳米氧化锆的作用是提高聚四氟乙烯摩擦材料的载荷承载力,进而提高其使用寿命。Based on the mass parts of the polytetrafluoroethylene, the preparation raw materials of the polytetrafluoroethylene friction material provided by the present invention include 1-5 parts of nano-zirconia, preferably 3-5 parts, more preferably 4-5 parts. In the present invention, the particle size of the nano-zirconia is preferably 20-40 nm, more preferably 25-35 nm. In the present invention, the role of the nano-zirconia is to improve the load bearing capacity of the PTFE friction material, thereby increasing its service life.
以所述聚四氟乙烯的质量份为基准,本发明提供的聚四氟乙烯摩擦材料的制备原料包括碳量子点1~5份,优选为2~5份,更优选为2~4份。在本发明中,所述碳量子点的粒径优选为3~5nm,更优选为3.5~4.5nm。在本发明中,所述碳量子点的作用是提高摩擦材料中各种填料与聚四氟乙烯间的界面结合强度。Based on the mass parts of the polytetrafluoroethylene, the preparation raw materials of the polytetrafluoroethylene friction material provided by the present invention include 1-5 parts of carbon quantum dots, preferably 2-5 parts, more preferably 2-4 parts. In the present invention, the particle size of the carbon quantum dots is preferably 3 to 5 nm, more preferably 3.5 to 4.5 nm. In the present invention, the role of the carbon quantum dots is to improve the interface bonding strength between various fillers in the friction material and polytetrafluoroethylene.
以所述聚四氟乙烯的质量份为基准,本发明提供的聚四氟乙烯摩擦材料的制备原料包括片层纳米Ti3C2 1~5份,优选为2~4份,更优选为2.5~3.5份。在本发明中,所述片层纳米Ti3C2的单层厚度优选为80~100nm,更优选为85~95nm。在本发明中,所述片层纳米Ti3C2的结构如图1所示。本发明添加片层纳米Ti3C2,片层纳米Ti3C2独特的二维层状结构使其具有优异的摩擦学特性,配合其他组分,得到的聚四氟乙烯摩擦材料可显著改善大型超声电机的启停特性。Based on the mass parts of the polytetrafluoroethylene, the preparation raw materials of the polytetrafluoroethylene friction material provided by the present invention include 1-5 parts, preferably 2-4 parts, and more preferably 2.5 parts of lamellar nano-Ti 3 C 2 . ~ 3.5 servings. In the present invention, the single-layer thickness of the lamellar nano-Ti 3 C 2 is preferably 80-100 nm, more preferably 85-95 nm. In the present invention, the structure of the lamellar nano-Ti 3 C 2 is shown in FIG. 1 . The invention adds lamella nano Ti 3 C 2 , and the unique two-dimensional layered structure of lamella nano Ti 3 C 2 makes it have excellent tribological properties, and with other components, the obtained PTFE friction material can be significantly improved Start-stop characteristics of large ultrasonic motors.
本发明优选采用江苏先丰纳米材料科技有限公司的碳量子点、纳米氮化硼、纳米氧化锆和片层纳米Ti3C2。The present invention preferably adopts carbon quantum dots, nano-boron nitride, nano-zirconia and lamellar nano-Ti 3 C 2 from Jiangsu Xianfeng Nano Material Technology Co., Ltd.
本发明提供了上述方案所述聚四氟乙烯摩擦材料的制备方法,包括以下步骤:将各制备原料进行混合,对得到的混合料依次进行压制和烧结,得到聚四氟乙烯摩擦材料。The present invention provides a method for preparing a polytetrafluoroethylene friction material according to the above scheme, which includes the following steps: mixing each preparation raw material, and sequentially pressing and sintering the obtained mixture to obtain a polytetrafluoroethylene friction material.
本发明将各制备原料进行混合,得到混合料。在本发明中,所述混合的过程优选为:将各制备原料分散到乙醇或丙酮中,干燥后得到混合料。本发明对所述分散的方式没有特殊要求,任意能够分散均匀的方式均可,如球磨、超声分散等。在本发明对所述乙醇或丙酮的用量没有特殊要求,能够将各制备原料混合均匀即可。在本发明中,所述干燥的温度优选为80~100℃,本发明对所述干燥的时间没有特殊要求,以乙醇或丙酮刚好蒸干为宜。In the present invention, each preparation raw material is mixed to obtain a mixed material. In the present invention, the mixing process is preferably as follows: each preparation raw material is dispersed into ethanol or acetone, and the mixture is obtained after drying. The present invention has no special requirements for the dispersion method, and any method that can disperse uniformly can be used, such as ball milling, ultrasonic dispersion, and the like. In the present invention, there is no special requirement for the amount of the ethanol or acetone, and all the preparation raw materials can be mixed uniformly. In the present invention, the drying temperature is preferably 80-100° C., and the present invention has no special requirements for the drying time, and ethanol or acetone is preferably just evaporated to dryness.
得到混合料后,本发明对所述混合料进行压制。本发明优选将混合料置于模具中进行压制。本发明对所述模具的形状没有特殊要求,本领域技术人员可根据摩擦材料的形状选择对应的模具。在本发明中,所述压制的压力优选为70~100MPa,更优选为80~100MPa,时间优选为3~5min,更优选为4~5min。After the mixture is obtained, the present invention compresses the mixture. In the present invention, the mixture is preferably placed in a mold for compression. The present invention has no special requirements on the shape of the mold, and those skilled in the art can select a corresponding mold according to the shape of the friction material. In the present invention, the pressing pressure is preferably 70-100 MPa, more preferably 80-100 MPa, and the time is preferably 3-5 min, more preferably 4-5 min.
完成所述压制后,本发明优选脱模,对脱模后所得压制坯进行烧结,得到聚四氟乙烯摩擦材料。在本发明中,所述烧结优选在空气氛围下进行;所述烧结的温度优选为365~375℃,更优选为368~372℃,保温时间优选为90~150min,更优选为95~145min。本发明优选自室温升至烧结的温度,本发明对升温的速率没有特殊要求。完成烧结后,本发明优选自由降至室温,得到聚四氟乙烯摩擦材料。After the pressing is completed, the present invention preferably demolds, and sinters the compact obtained after demolding to obtain a polytetrafluoroethylene friction material. In the present invention, the sintering is preferably carried out in an air atmosphere; the sintering temperature is preferably 365-375° C., more preferably 368-372° C., and the holding time is preferably 90-150 min, more preferably 95-145 min. In the present invention, the temperature is preferably raised from room temperature to the sintering temperature, and the present invention has no special requirements on the rate of temperature increase. After the sintering is completed, the present invention preferably freely reduces to room temperature to obtain a polytetrafluoroethylene friction material.
本发明提供了上述方案所述聚四氟乙烯摩擦材料或上述方案所述制备方法制备得到的聚四氟乙烯摩擦材料在超声电机中的应用。在本发明中,所述超声电机优选为大型超声电机(直径在150mm以上)。本发明对所述应用的方式没有特殊要求,采用本领域熟知的应用方式即可。The present invention provides the application of the polytetrafluoroethylene friction material in the above scheme or the polytetrafluoroethylene friction material prepared by the preparation method in the above scheme in an ultrasonic motor. In the present invention, the ultrasonic motor is preferably a large ultrasonic motor (with a diameter of more than 150 mm). The present invention has no special requirements on the application mode, and an application mode well known in the art can be adopted.
下面结合实施例对本发明提供的聚四氟乙烯摩擦材料及其制备方法和应用进行详细的说明,但是不能把它们理解为对本发明保护范围的限定。The polytetrafluoroethylene friction material provided by the present invention and its preparation method and application will be described in detail below with reference to the examples, but they should not be construed as limiting the protection scope of the present invention.
实施例1Example 1
称取聚四氟乙烯80g、纳米氮化硼2g、二硫化钼10g、纳米氧化锆3g、碳量子点4g、片层纳米Ti3C2 1g,在无水乙醇中混合均匀,干燥后将混合好的粉料放入模具,在70MPa的压力下,压制3min,脱模后放入烧结炉中烧结,由室温逐步升温至365℃,并在365℃保温90min,烧结结束后自由降温,得到聚四氟乙烯摩擦材料。Weigh 80 g of polytetrafluoroethylene, 2 g of nano-boron nitride, 10 g of molybdenum disulfide, 3 g of nano-zirconia, 4 g of carbon quantum dots, and 1 g of lamellar nano-Ti 3 C 2 , mix them evenly in absolute ethanol, and mix them after drying. Put the good powder into the mold, press it for 3 minutes under the pressure of 70MPa, put it into the sintering furnace for sintering after demoulding, gradually heat up from room temperature to 365 ℃, and keep it at 365 ℃ for 90 minutes, after the sintering, it is free to cool down to obtain the polymer powder. Teflon friction material.
实施例2Example 2
称取聚四氟乙烯75g、纳米氮化硼5g、二硫化钼10g、纳米氧化锆5g、碳量子点3g、片层纳米Ti3C2 2g,在无水乙醇中混合均匀,干燥后将混合好的粉料放入模具,在100MPa的压力下,压制5min,脱模后放入烧结炉中烧结,由室温逐步升温至375℃,并在375℃保温150min,烧结结束后自由降温,得到聚四氟乙烯摩擦材料。Weigh 75g of polytetrafluoroethylene, 5g of nano-boron nitride, 10g of molybdenum disulfide, 5g of nano-zirconia, 3g of carbon quantum dots, and 2g of lamellar nano-Ti 3 C 2 , mix them well in absolute ethanol, and mix them after drying. Put the good powder into the mold, press it for 5 minutes under the pressure of 100MPa, put it into the sintering furnace for sintering after demoulding, gradually heat it up from room temperature to 375 °C, and keep it at 375 °C for 150 minutes, after the sintering, it is free to cool down to obtain a polymer. Teflon friction material.
实施例3Example 3
称取聚四氟乙烯70g、纳米氮化硼5g、二硫化钼15g、纳米氧化锆5g、碳量子点2g、片层纳米Ti3C2 3g,在无水乙醇中混合均匀,干燥后将混合好的粉料放入模具,在95MPa的压力下,压制4min,脱模后放入烧结炉中烧结,由室温逐步升温至370℃,并在370℃保温120min,烧结结束后自由降温,得到聚四氟乙烯摩擦材料。Weigh 70 g of polytetrafluoroethylene, 5 g of nano-boron nitride, 15 g of molybdenum disulfide, 5 g of nano-zirconia, 2 g of carbon quantum dots, and 3 g of lamellar nano-Ti 3 C 2 , mix them well in absolute ethanol, and mix them after drying. Put the good powder into the mold, press it for 4 minutes under the pressure of 95MPa, put it into the sintering furnace for sintering after demoulding, gradually heat up from room temperature to 370 ° C, and keep it at 370 ° C for 120 minutes, after the sintering, it is free to cool down to obtain a polymer. Teflon friction material.
实施例4Example 4
称取聚四氟乙烯66g、纳米氮化硼5g、二硫化钼15g、纳米氧化锆5g、碳量子点5g、片层纳米Ti3C2 4g,在无水乙醇中混合均匀,干燥后将混合好的粉料放入模具,在80MPa的压力下,压制3min,脱模后放入烧结炉中烧结,由室温逐步升温至365℃,并在365℃保温100min,烧结结束后自由降温,得到聚四氟乙烯摩擦材料。Weigh 66g of polytetrafluoroethylene, 5g of nano-boron nitride, 15g of molybdenum disulfide, 5g of nano-zirconia, 5g of carbon quantum dots, and 4g of lamellar nano-Ti 3 C 2 , mix them well in absolute ethanol, and mix them after drying. Put the good powder into the mold, press it for 3 minutes under the pressure of 80MPa, put it into the sintering furnace for sintering after demoulding, gradually heat up from room temperature to 365 ℃, and keep it at 365 ℃ for 100 minutes, after the sintering, it is free to cool down to obtain the polymer powder. Teflon friction material.
实施例5Example 5
称取聚四氟乙烯70g、纳米氮化硼4g、二硫化钼15g、纳米氧化锆1g、碳量子点5g、片层纳米Ti3C2 5g,在无水乙醇中混合均匀,干燥后将混合好的粉料放入模具,在75MPa的压力下,压制5min,脱模后放入烧结炉中烧结,由室温逐步升温至375℃,并在375℃保温110min,烧结结束后自由降温,得到聚四氟乙烯摩擦材料。Weigh 70g of polytetrafluoroethylene, 4g of nano-boron nitride, 15g of molybdenum disulfide, 1g of nano-zirconia, 5g of carbon quantum dots, and 5g of lamellar nano-Ti 3 C 2 , mix them well in absolute ethanol, and mix them after drying. Put the good powder into the mold, press it for 5 minutes under the pressure of 75MPa, put it into the sintering furnace for sintering after demolding, gradually heat up from room temperature to 375 ° C, and keep it at 375 ° C for 110 minutes, after the sintering is completed, it is free to cool down to obtain the polymer powder. Teflon friction material.
对比例1Comparative Example 1
称取聚四氟乙烯73g、纳米氮化硼5g、二硫化钼15g、纳米氧化锆5g、碳量子点2g,在无水乙醇中混合均匀,干燥后将混合好的粉料放入模具,在95MPa的压力下,压制4min,脱模后放入烧结炉中烧结,由室温逐步升温至370℃,并在370℃保温120min,烧结结束后自由降温,得到聚四氟乙烯摩擦材料。Weigh 73 g of polytetrafluoroethylene, 5 g of nano-boron nitride, 15 g of molybdenum disulfide, 5 g of nano-zirconia, and 2 g of carbon quantum dots, mix them evenly in absolute ethanol, and put the mixed powder into the mold after drying. Under the pressure of 95MPa, press for 4 minutes, put it into a sintering furnace for sintering after demoulding, gradually heat up from room temperature to 370 ° C, and keep it at 370 ° C for 120 minutes, and freely cool down after sintering to obtain PTFE friction material.
对实施例1~5和对比例1制备的聚四氟乙烯摩擦材料进行启停性测试,测试条件:采用的超声电机为大型超声电机(直径为150mm),聚四氟乙烯摩擦材料与磷青铜对磨,磨合时间40h,转速120r/min。磨合后电机停止2h,然后重新启动电机并测量此时的静摩擦力矩以及运动后的动摩擦力矩,摩擦力矩为3~5次测试的平均值。具体的测试结果见表1。The PTFE friction materials prepared in Examples 1 to 5 and Comparative Example 1 were tested for start-stop performance. The test conditions were as follows: the ultrasonic motor used was a large ultrasonic motor (diameter of 150 mm), and the PTFE friction material and phosphor bronze were used. For grinding, the running-in time is 40h, and the speed is 120r/min. After running-in, the motor stops for 2 hours, then restarts the motor and measures the static friction torque at this time and the dynamic friction torque after exercise. The friction torque is the average value of 3 to 5 tests. The specific test results are shown in Table 1.
表1 实施例及对比例制备的摩擦材料对超声电机启停特性的影响Table 1 Influence of friction materials prepared in Examples and Comparative Examples on the start-stop characteristics of ultrasonic motors
动静摩擦力矩越接近,超声电机的启停特性越好。通过实施例和对比例可以发现,片层纳米Ti3C2能够明显的提高超声电机的启停特性。此外,从实施例还可以发现,片层纳米Ti3C2并不是越多越好,含量较高会发生团聚影响性能,含量较少时改善作用不明显。The closer the static and dynamic friction torque is, the better the start-stop characteristics of the ultrasonic motor. Through the examples and comparative examples, it can be found that the lamellar nano-Ti 3 C 2 can significantly improve the start-stop characteristics of the ultrasonic motor. In addition, it can also be found from the examples that the more nano-Ti 3 C 2 in the lamellae is not the better, the higher the content, the agglomeration will affect the performance, and the improvement effect is not obvious when the content is less.
以上所述仅是本发明的优选实施方式,应当指出,对于本技术领域的普通技术人员来说,在不脱离本发明原理的前提下,还可以做出若干改进和润饰,这些改进和润饰也应视为本发明的保护范围。The above are only the preferred embodiments of the present invention. It should be pointed out that for those skilled in the art, without departing from the principles of the present invention, several improvements and modifications can be made. It should be regarded as the protection scope of the present invention.
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Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1935939A4 (en) * | 2005-10-12 | 2011-03-23 | Nok Corp | PTFE RESIN COMPOSITION |
CN103756209A (en) * | 2013-12-18 | 2014-04-30 | 安徽南方化工泵业有限公司 | Wearproof and high temperature resistant modified polytetrafluoroethylene material for pumps and valves |
CN107099054A (en) * | 2017-05-12 | 2017-08-29 | 深圳大学 | Ti3C2The preparation method of MXene/ polymer composite wave-suction materials |
CN109777013A (en) * | 2019-02-22 | 2019-05-21 | 中国科学院兰州化学物理研究所 | A kind of graphene-modified polytetrafluoroethylene oil seal lip material and preparation method thereof |
CN109825014A (en) * | 2019-03-19 | 2019-05-31 | 中国科学院兰州化学物理研究所 | A kind of high elastic modulus polytetrafluoroethylene friction material and its preparation method and application |
CN109851962A (en) * | 2019-03-19 | 2019-06-07 | 中国科学院兰州化学物理研究所 | One type graphene nano carbonitride modified Teflon friction material and its preparation method and application |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE19950622A1 (en) * | 1999-10-20 | 2001-05-31 | Schott Glas | Friction lining for components in brake systems |
WO2014147221A2 (en) * | 2013-03-22 | 2014-09-25 | Esk Ceramics Gmbh & Co. Kg | Friction-reducing polymer material with dry-running capability and mechanical end-face seal with dry-running capability |
CN103289260B (en) * | 2013-05-07 | 2015-11-04 | 浙江大学 | Preparation method of ultrafine zeolite powder filled PTFE composite material |
-
2020
- 2020-03-13 CN CN202010175887.3A patent/CN111333982B/en active Active
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1935939A4 (en) * | 2005-10-12 | 2011-03-23 | Nok Corp | PTFE RESIN COMPOSITION |
CN103756209A (en) * | 2013-12-18 | 2014-04-30 | 安徽南方化工泵业有限公司 | Wearproof and high temperature resistant modified polytetrafluoroethylene material for pumps and valves |
CN107099054A (en) * | 2017-05-12 | 2017-08-29 | 深圳大学 | Ti3C2The preparation method of MXene/ polymer composite wave-suction materials |
CN109777013A (en) * | 2019-02-22 | 2019-05-21 | 中国科学院兰州化学物理研究所 | A kind of graphene-modified polytetrafluoroethylene oil seal lip material and preparation method thereof |
CN109825014A (en) * | 2019-03-19 | 2019-05-31 | 中国科学院兰州化学物理研究所 | A kind of high elastic modulus polytetrafluoroethylene friction material and its preparation method and application |
CN109851962A (en) * | 2019-03-19 | 2019-06-07 | 中国科学院兰州化学物理研究所 | One type graphene nano carbonitride modified Teflon friction material and its preparation method and application |
Non-Patent Citations (3)
Title |
---|
"Effects of various fillers on the sliding wear of polymer composites";Friedrich, K,et.al;《COMPOSITES SCIENCE AND TECHNOLOGY》;20050728;第65卷(第15-16期);第2329-2343页 * |
"Preparation, mechanical and anti-friction performance of";Heng Zhang,et.al;《Materials and Design》;20151217;第682-689页 * |
"填料粒径对Cu/PTFE复合材料摩擦学性能影响的数值模拟";解挺等;《摩擦学学报》;20160131;第36卷(第1期);第35-41页 * |
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