压力和温度对再生材料制备的碳-碳复合材料性能的影响

D. Manohar, V. Raju
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引用次数: 3

摘要

以黄麻纤维-酚醛树脂为原料,采用程控碳化法制备了碳-碳复合材料。采用手工铺层法制备黄麻/酚醛树脂复合材料,并在160℃、460 bar的压力下在压缩机中固化。碳化循环设计采用TGA研究,在3-20°C / min的不同加热速率下进行高达800°C的碳化循环。碳化实验在管式炉和热压机上进行。复合材料在热压机中以程序升温速率在室温至800℃的压力下进行碳化,部分碳化的复合材料在管式炉中以程序升温速率在氩气中不施加室温至1000℃的压力下进一步碳化。对复合材料的密度、官能团、碳化程度、石墨化程度、孔隙率和导电性进行了表征。结果表明,碳化前复合材料的密度为1.30 g/cc,碳化后分别降至0.78 g/cc和0.97 g/cc,说明了由于挥发分逸出造成的重量损失。红外光谱研究表明,碳化复合材料中CH、C- oh等官能团转变为芳香族C=C、C≡C。拉曼光谱显示了碳化复合材料中石墨结构的证据。无压力碳化的复合材料表面孔隙大小在82 ~ 312 μm之间,有压力碳化的复合材料表面孔隙大小减小到42 ~ 93 μm。在碳化过程中,复合材料的电导率也从4.7 × 10 - 12 S/cm增加到1.429 × 10 - 2 S/cm和6.777 × 10 - 2 S/cm。
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Effect of pressure and temperature on properties of carbon-carbon composites prepared from renewable material
This paper presents the preparation of carbon-carbon composites (CCC) from jute fibre — phenol formaldehyde (PF) resin by programmed carbonisation process. Jute/PF resin composite was prepared using hand layup technique followed by curing in compression press at 160°C under pressure of 460 bar. Carbonisation cycle was designed using TGA studies carried out up to 800°C at different heating rates in the range of 3–20 °C / min. Carbonisation experiments were carried out in both tubular furnace and hot press. Carbonisation of the composite was performed at a programmed heating rate in a hot press with application of pressure from room temperature to 800°C, the partially carbonized composite was further carbonized in the tubular furnace without application of pressure from room temperature to 1000°C in argon atmosphere under programmed heating rate. The resulting composites were characterized for density, functional groups, extent of carbonisation, graphitization, porosity and conductivity. The results show that the density of the composite before carbonisation was 1.30 g/cc which was reduced to 0.78 g/cc and 0.97 g/cc after carbonisation without and with pressure respectively indicating the weight loss due to the escape of the volatiles. The transformation of functional groups such as CH, C-OH etc to aromatic C=C, C≡C in carbonized composite was evident from FTIR studies. Raman spectra shows the evidence of graphitic structure in the carbonized composites. Surface pores in the range of 82 to 312 μm were noticed in the composite carbonised without pressure and the pore sizes were reduced to 42 to 93 μm when carbonized under pressure. Electrical conductivity also increases from 4.7 × 10−12 S/cm to 1.429 × 10−2 S/cm and 6.777 × 10−2 S/cm for the composite carbonised without and with pressure during carbonisation.
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