• Bulletin of the Korean Chemical Society
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• 제23권12호
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• pp.1801-1805
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• 2002

The graphite intercalation compounds(GIC) were prepared by a dry process that led to the intercalation from the direct reaction of gaseous $SO_3$ with flake type graphite. The basal spacing of the GIC was increased from 8.3 ${\AA}$ to 12 in the gallery height. The ejection of interlayer $SO_3$ molecules by the heating for 1 minute at $950^{\circ}C$ resulted in an exfoliated graphite (EG) with surprisingly high expansion in the direction of c-axis. The expansion ratios of the exfoliated graphites were increased greatly between 220 times and 400 times compared to the original graphite particles, and the bulk density was range of 0.0053 to 0.01 $g/cm^3$, depending on reaction time. The pore size distribution of exfoliated graphite was in the range of $10-170{\mu}m$, which exhibites both mesoporosity and macroporosities. This result indicates that the direct reaction of graphite paricles with gaseous $SO_3$ can be proposed as an another route for the exfoliated graphite having excellent physical properties.

• Carbon letters
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• 제2권1호
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• pp.55-60
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• 2001

Graphite intercalation compounds (GIC) were prepared by direct reaction of $SO_3$ gas with flake graphite. The intercalated $SO_3$ molecules were ejected by rapid heating to $950^{\circ}C$ under an oxidizing atmosphere for about 1 minute, resulting in surprisingly high expansion in the direction of c-axis. The characteristics of the micro-structure and pore size distribution were examined with a SEM and mercury intrusion porosimetry. The XRD analysis and spectroscopic analysis were used for the identification of the graphite and surface chemistry state. The pore size distribution of the exfoliated graphite (EG) was a range of $1{\sim}170{\mu}m$. The higher expanding temperature the higher expanded volume, so oil sorption capacities were 58.8 g of bunker-C oil and 34.7 g of diesel oil per 1 g of the the EG. The sorption equilibrium was achieved very rapidly within several minutes. As the treatment temperature increases, bulk density decreases.

• 대한환경공학회지
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• 제36권1호
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• pp.1-6
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• 2014

팽창흑연과 탄소나노튜브를 이용한 복합 산화전극을 나피온용액에 다양한 비율로 에폭시를 혼합한 결합제를 이용하여 제작하였으며, 산화전극 결합제에 함유된 에폭시량이 미생물연료전지의 성능에 미치는 영향을 회분식 실험을 통하여 조사하였다. 산화전극 결합제에 에폭시의 함량이 증가함에 따라 산화전극 구성 물질들의 물리적 부착력은 점차 증가하였으나, 활성화저항과 오옴저항의 증가로 인한 내부저항이 증가하였다. 산화전극 결합제로 에폭시를 혼합하지 않고 나피온용액 만을 사용한 대조구의 경우 $1,892mW/m^2$에 달하였으나 산화전극 결합제에 에폭시 함량이 증가함에 따라 미생물연료전지의 최대전력밀도는 점차 감소하였다. 산화전극 결합제에 에폭시함량이 50%일 때 최대전력밀도는 $1,425mW/m^2$로서 대조구의 75.3%까지 감소하였으나, 고가의 나피온용액 사용량을 감소시키고 산화전극 결합제의 물리적 부착력을 높일 수 있다는 측면에서 고려할 때 나피온용액과 에폭시를 같은 비율로 혼합한 물질은 산화전극결합제로서의 좋은 대안이 될 수 있는 것으로 판단된다.