Conductive polymer composites with high electrical and mechanical properties are in demand for bipolar plates of phosphoric acid fuel cells (PAFC). In this study, composites based on natural graphite/fluorinated ethylene propylene (FEP) and different ratios of carbon black are mixed and hot formed into bars. The overall content of natural graphite is replaced by carbon black (0.2 wt% to 3.0 wt%). It is found that the addition of carbon black reduces electrical resistivity and density. The density of composite materials added with carbon black 3.0 wt% is 2.168 g/cm3, which is 0.017 g/cm3 less than that of non-additive composites. In-plane electrical resistivity is 7.68 μΩm and through-plane electrical resistivity is 27.66 μΩm. Compared with non-additive composites, in-plane electrical resistivity decreases by 95.7 % and through-plane decreases by 95.9 %. Also, the bending strength is about 30 % improved when carbon black is added at 2.0 wt% compared to non-additive cases. The decrease of electrical resistivity of composites is estimated to stem from the carbon black, which is a conductive material located between melted FEP and acts a path for electrons; the increasing mechanical properties are estimated to result from carbon black filling up pores in the composites.
Numerous studies have reported that good adhesion and fluorination of carbon materials in a fluoropolymer matrix enhance their electrical and mechanical properties. However, a composite reinforced with oxyfluorinated graphite has not been reported for improving mechanical properties. This paper discusses the fabrication of conductive fluorinated ethylene–propylene (FEP)/oxyfluorinated graphite (f-graphite) composite bipolar plates (BPs) via compression molding. To investigate the effects of fluorinating graphite, graphite with a large particle size of 500 μm was mixed with FEP powder with a small particle size of 8 μm through ball milling. The FEP/graphite composites exhibited high anisotropic electrical conductivity with the in-plane conductivity much higher than the through-plane conductivity because of the planar orientation of the graphite sheets. Therefore, the mechanical properties of the composites such as flexural strength tended to deteriorate with increasing graphite content. In particular, the FEP/f-graphite composites exhibited excellent flexural strength of 12 MPa, much higher than that of FEP/graphite composites at 9 MPa with a graphite content of 80 wt%. The interfacial interaction between FEP and f-graphite led to improved physical compatibilization, which contributed to enhance the mechanical properties of these composites. Our results are a step toward developing BPs for use in high-temperature fuel cells and heat-sink components.
A composite material was prepared for the bipolar plates of phosphoric acid fuel cells(PAFC) by hot pressing a flake type natural graphite powder as a filler material and a fluorine resin as a binder. Average particle sizes of the powders were 610.3, 401.6, 99.5, and 37.7 μm. The density of the composite increased from 2.25 to 2.72 g/cm3 as the graphite size increased from 37.7 to 610.3 μm. The anisotropy ratio of the composite increased from 1.8 to 490.9 as the graphite size increased. The flexural strength of the composite decreased from 15.60 to 8.94MPa as the graphite size increased. The porosity and the resistivity of the composite showed the same tendencies, and decreased as the graphite size increased. The lowest resistivity and porosity of the composite were 1.99 × 10−3 Ωcm and 2.02 %, respectively, when the graphite size was 401.6 μm. The flexural strength of the composite was 10.3MPa when the graphite size was 401.6 μm. The lowest resistance to electron mobility was well correlated with the composite with lowest porosity. It was possible the flaky large graphite particles survive after the hot pressing process.
본 연구에서는 흑연, 열경화성 수지, 그리고 카본 블랙을 사용하여 조성과 제조 조건을 달리하여서 탄소 복합체를 제조하였다. 제조된 탄소 복합체의 고분자 전해질 연료전지용 bipolar plate로의 응용 가능성을 살펴보기 위하여 연속 흐름 기체 투과 장치를 사용하여서 산소의 투과도를 측정하였다 실험 결과 카본 블랙의 양이 증가할수록 산소 투과도가 증가하였으며, 탄소 복합체의 성형 시간이 증가할수록 투과도가 감소하였다 반면에 성형 압력은 산소 투과도에 큰 영향을 미치지 않음을 알 수 있었다.