Ania Conchi O, Bandosz Teresa J
Department of Chemistry, The City College of New York, and The Graduate School of the City University of New York, New York, New York 10031, USA.
Langmuir. 2005 Aug 16;21(17):7752-9. doi: 10.1021/la050772e.
The performance of various activated carbons obtained from different carbon precursors (i.e., plastic waste, coal, and wood) as adsorbents for the desulfurization of liquid hydrocarbon fuels was evaluated. To increase surface heterogeneity, the carbon surface was modified by oxidation with ammonium persulfate. The results showed the importance of activated carbon pore sizes and surface chemistry for the adsorption of dibenzothiophene (DBT) from liquid phase. Adsorption of DBT on activated carbons is governed by two types of contributions: physical and chemical interactions. The former include dispersive interactions in the microporous network of the carbons. While the volume of micropores governs the amount physisorbed, mesopores control the kinetics of the process. On the other hand, introduction of surface functional groups enhances the performance of the activated carbons as a result of specific interactions between the acidic centers of the carbon and the basic structure of DBT molecule as well as sulfur-sulfur interactions.
评估了由不同碳前驱体(即塑料废料、煤和木材)制得的各种活性炭作为液态烃燃料脱硫吸附剂的性能。为了增加表面不均匀性,用过硫酸铵氧化对碳表面进行了改性。结果表明活性炭孔径和表面化学性质对于从液相中吸附二苯并噻吩(DBT)的重要性。DBT在活性炭上的吸附受两种作用的支配:物理和化学相互作用。前者包括碳微孔网络中的色散相互作用。虽然微孔体积决定了物理吸附量,但中孔控制着该过程的动力学。另一方面,表面官能团的引入由于碳的酸性中心与DBT分子的基本结构之间的特定相互作用以及硫-硫相互作用而提高了活性炭的性能。