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Activated carbon surface heterogeneity seen by parallel probing by inverse liquid chromatography at the solid/liquid interface and by gas adsorption analysis at the solid/gas interface

机译:通过在固/液界面进行反相液相色谱和在固/气界面进行气体吸附分析进行平行探测,可以看到活性炭表面的异质性

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摘要

The energetic surface heterogeneity of four different activated carbons was assessed by the parallel probing at the solid/liquid and solid/gas interfaces. At the solid/liquid interface a method of inverse liquid chromatography, frontal analysis by characteristic point was applied using phenylalanine in water solution as a probe molecule. At the solid/gas interface, argon was used as a probe in the low pressure quasi equilibrium volumetry method. The treatment of the adsorption isotherms by the derivative isotherm summation procedure revealed similar adsorption energy distributions for both argon and phenylalanine. Such an agreement between both methods suggests that, at the solid/liquid interface and on the solid/gas interface, the adsorption was mainly controlled by geometric parameters and no specific interaction was observed and physisorbed water did not played a significant role in adsorption process on three from four studied carbons.
机译:通过在固体/液体和固体/气体界面处的平行探测,评估了四种不同活性炭的高能表面异质性。在固/液界面上,采用反相液相色谱法,使用水溶液中的苯丙氨酸作为探针分子,通过特征点进行正面分析。在固/气界面处,氩气用作低压准平衡体积法中的探针。通过导数等温线求和过程对吸附等温线的处理表明,氩气和苯丙氨酸的吸附能分布相似。两种方法之间的这种一致性表明,在固/液界面和固/气界面上,吸附主要受几何参数控制,未观察到特定的相互作用,并且物理吸附水在吸附过程中没有发挥重要作用。四个研究碳中的三个。

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