Nitrate uptake improvement by modified activated carbons developed from two species of pine cones

被引:74
作者
Nunell, G. V. [1 ,2 ]
Fernandez, M. E. [1 ,2 ]
Bonelli, P. R. [1 ,2 ]
Cukierman, A. L. [1 ,2 ,3 ]
机构
[1] Univ Buenos Aires, Fac Ciencias Exactas & Nat, Dept Ind, Programa Invest & Desarrollo Fuentes Alternat Mat, RA-1053 Buenos Aires, DF, Argentina
[2] Consejo Nacl Invest Cient & Tecn, RA-1033 Buenos Aires, DF, Argentina
[3] Univ Buenos Aires, Fac Farm & Bioquim, Dept Tecnol Farmaceut, Catedra Farmacotecn 2, RA-1053 Buenos Aires, DF, Argentina
关键词
Nitrate adsorption; Modified activated carbons; Urea treatment; Thermal treatment; SURFACE MODIFICATION; AQUEOUS-SOLUTIONS; REMOVAL; ADSORPTION; NITROGEN; WASTE; WATER; DYES; CONTAMINATION; GROUNDWATER;
D O I
10.1016/j.jcis.2014.10.058
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Activated carbons from two species of pine cones (Pinus canariensis and Cupressus sempervirens) were prepared by phosphoric acid activation and tested for the removal of nitrate ions from aqueous solution. To investigate the feasibility of improving their nitrate adsorption capacity, two different post-treatments a thermal treatment and a treatment with saturated urea solution - were also applied to the prepared activated carbons. Comparison of the treated and untreated activated carbons showed that both post-treatments improved the nitrate adsorption performance more than twice. The maximum adsorption capacity, as evaluated from determination of the adsorption isotherms for the P. canariensis based carbons, and their proper representation by the Langmuir model, demonstrated that the post-treatment with the urea solution led to activated carbons with increased nitrate removal effectiveness, even superior to other reported results. Enhancements in their adsorption capacity could be mainly ascribed to higher contents of nitrogen and basic functional groups, whereas porous structure of the activated carbons did not seem to play a key role in the nitrate uptake. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:102 / 108
页数:7
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