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The Microporosity of Activated Carbon Fibre KF1500 Assessed by Combined CO2 Adsorption and Calorimetry Techniques and by Immersion Calorimetry

机译:活性炭纤维KF1500的微孔率通过CO 2 吸附和量热技术和浸没量热法联合评估

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摘要

The microporous structure of the activated carbon fibre KF1500 was investigated by applying a new technique as presented here. This was based on a combination of high-pressure CO adsorption measurements between 253 K and 353 K with direct measurement of the differential heats of adsorption at 298 K at low and medium coverages. The validity of this approach was tested by using two activated carbons which has been characterized previously by a variety of techniques, including immersion calorimetry. It appears that a combination of high-pressure adsorption and calorimetry with CO alone is a useful tool for the characterization of the whole range of microporosity. This approach confirms earlier observations, according to which the initial stage of adsorption by strongly activated carbons corresponds to adsorption on the walls of large micropores rather than to the primary filling of small micropores.
机译:活性炭纤维KF1500的微孔结构通过应用此处介绍的新技术进行了研究。这是基于253 K和353 K之间的高压CO吸附测量值与直接测量中低覆盖率下298 K的吸附差热的组合。通过使用两种活性炭测试了该方法的有效性,这两种活性炭先前已通过多种技术(包括浸没量热法)进行了表征。似乎高压吸附和量热法与单独的CO的组合是表征整个微孔率范围的有用工具。这种方法证实了较早的观察结果,据此,强活性炭吸附的初始阶段对应于大微孔壁上的吸附,而不是小微孔的初次填充。

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