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Preparation of microfibrous entrapped activated carbon composite

机译:包裹微纤维的活性炭复合材料的制备

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A kind of microfibrous entrapped activated carbon composites were prepared by the wet lay-up paper-making process followed by sintering in N2 at 950 °C for 30 min. SEM and ASAP 2020 apparatus were used to characterize the structure and test the adsorption isotherm. SEM results indicated that the junctures of the ceramic fiber were completely welded together to cause a sinter-locked three-dimensional network, thereby entrapping micron-sized activated carbon. The porous structure was analyzed with BET equations, H-K equation and BJH theory. Results showed that the specific surface area was 428 m2/g, the total pore volume was 0.217 m3/g, the total micropore volume was 0.0935 m3/g which was 43.1% of the total pore volume, the mesopore volume was 40.9% and the macropore volume was 16.0%. Compared between microfibrous composite and primary activated carbon, the surface areas and the pore structure were almost the same, but the pore volumes all decreased.
机译:通过湿式抄纸工艺制备一种微纤维夹带活性炭复合材料,然后在950°C的N2中烧结30分钟。使用SEM和ASAP 2020仪器表征结构并测试吸附等温线。 SEM结果表明,陶瓷纤维的接合处被完全焊接在一起,形成了烧结锁定的三维网络,从而截留了微米级的活性炭。用BET方程,H-K方程和BJH理论分析了多孔结构。结果表明,比表面积为428 m2 / g,总孔体积为0.217 m3 / g,总微孔体积为0.0935 m3 / g,占总孔体积的43.1%,中孔体积为40.9%,大孔体积为16.0%。与微纤维复合材料和初级活性炭相比,表面积和孔结构几乎相同,但孔体积均减小。

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