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Highly Filled Graphene-Benzoxazine Composites as Bipolar Plates in Fuel Cell Applications

机译:高填充石墨烯-苯并恶嗪复合材料作为双极板在燃料电池中的应用

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This research emphasizes on the development of highly filled graphene-polybenzoxazine composites and investigates thermal, electrical, and mechanical properties of the obtained composites for bipolar plate applications. The composition of graphene loading was achieved to be in the range of 10-60 wt%. The experimental results revealed that at the maximum graphene content of 60 wt% (44.8 vol%) in the poly-benzoxazine, storage moduli at room temperature of the composites were considerably enhanced with the amount of the graphene, that is, from 5.9 GPa of the neat polybenzoxazine to about 25.1 GPa at 60 wt% of graphene. Glass transition temperatures (T-g) of the obtained composites were observed to be 174-188 degrees C and the values substantially increased with increasing the filler contents. At 60 wt% of graphene content, thermal conductivity, as high as 8.0 W/mK, is achieved for the graphene-filled polybenzoxazine. Furthermore, the flexural modulus and flexural strength of the composites were found to be as high as 18 GPa and 42 MPa, respectively. Water absorption of graphene filled-composite is relatively low with the value of only about 0.06% at 24 h of water immersion. Additionally, electrical conductivity was measured to be 357 S/cm at maximum loading of the graphene. Therefore, the graphene-filled composites based on polybenzoxazine are highly attractive as bipolar plates for polymer electrolyte membrane fuel cells applications. (C) 2014 Society of Plastics Engineers
机译:这项研究着重于高填充石墨烯-聚苯并恶嗪复合材料的开发,并研究了所得复合材料在双极板应用中的热,电和机械性能。石墨烯负载量的组成达到10-60重量%。实验结果表明,在聚苯并恶嗪中最大石墨烯含量为60 wt%(44.8 vol%)时,复合材料在室温下的储能模量随着石墨烯的量而大大提高,即从5.9 GPa降低。在60%的石墨烯下,纯净的聚苯并恶嗪达到约25.1 GPa。观察到所得复合材料的玻璃化转变温度(T-g)为174-188℃,并且该值随着填料含量的增加而显着增加。石墨烯含量为60 wt%时,填充石墨烯的聚苯并恶嗪的导热系数高达8.0 W / mK。此外,发现复合材料的弯曲模量和弯曲强度分别高达18 GPa和42 MPa。石墨烯填充复合材料的吸水率相对较低,浸水24 h的吸水率仅为0.06%。另外,在石墨烯的最大负载下测得的电导率为357 S / cm。因此,基于聚苯并恶嗪的石墨烯填充复合材料作为用于聚合物电解质膜燃料电池应用的双极板极具吸引力。 (C)2014年塑料工程师学会

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