Journal of South China University of Technology(Natural Science) >
Adsorption of Dibenzothiophene in Acetonitrile on Fe3+ / Cu2+ / Ag+ -Modified Activated Carbons with High Specific Surface Area
Received date: 2012-04-10
Revised date: 2012-09-09
Online published: 2012-12-03
Supported by
国家自然科学基金资助项目(20806026);广东省自然科学基金资助项目(8251064101000018);广东省绿色化学产品技术重点实验室项目(GC201105)
In this paper, first, activated carbon (AC) with high specific surface area was modified with metal ionsFe3+,Cu2+ and Ag+ through an impregnation process, and three kinds of modified AC, namely, Fe3+ / AC, Cu2+ / ACand Ag+ / AC, were prepared. Next, the products were used to adsorb the dibenzothiophene (DBT) in acetonitrilesolution, and the corresponding isotherms were obtained by means of the static adsorption method. Then, the de-sorption peak areas of DBT desorbed from the AC before and after the modification were measured through tempera-ture-programmed desorption (TPD) experiments. Finally, the total amount of acidic functional groups on the sur-faces of these four kinds of AC was measured via the Boehm titration. The results show that, after the modification,both the total amount of acidic functional groups and the adsorption capacity for DBT increase, that the total amountof acidic functional groups follows the order of Fe3+ / AC>Cu2+ / AC>Ag+ / AC>AC, with the adsorption capacity re-spectively increasing by 30%, 20% and 14%. It is thus concluded that the adsorption capacity of AC absorbents isproportional to the total amount of acidic functional groups, and that the loading of Fe3+,Cu2+ and Ag+ on AC en-hances the adsorption of DBT in acetonitrile solution due to the increase of active sites on AC surfaces for DBT ad-sorption.
Key words: activated carbon; surface modification; adsorption; dibenzothiophene; acetonitrile
Li Zhong Zhang Hong Xia Qi-bin Zhang Wei Yu Mo-xin . Adsorption of Dibenzothiophene in Acetonitrile on Fe3+ / Cu2+ / Ag+ -Modified Activated Carbons with High Specific Surface Area[J]. Journal of South China University of Technology(Natural Science), 2013 , 41(1) : 100 -104,111 . DOI: 10.3969/j.issn.1000-565X.2013.01.016
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