Effect of some additives on synthesis of zeolite from coal fly ash

被引:44
|
作者
Wu, Deyi [1 ]
Zhang, Bohua [1 ]
Yan, Li [1 ]
Kong, Hainan [1 ]
Wang, Xinze [1 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Environm Sci & Engn, Shanghai 200240, Peoples R China
关键词
additive; zeolite; synthesis; fly ash; waste solution;
D O I
10.1016/j.minpro.2006.05.005
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Hydrothermal conversion of fly ash into zeolites was conducted and the effects of the addition of sodium halide and waste solutions produced after zeolitization of fly ash, as well as the adjustment of the Si/Al ratio prior to synthesis process on the formation and cation exchange capacity (CEC) of zeolite product were evaluated. Both the addition of NaCl and NaF ameliorated the crystallinity and CEC of synthesized zeolite, but NaF had a better improvement effect. Na+ was considered to enhance the crystallization of zeolite, while F- favored the dissolution of fly ash. The type of zeolite formed depended on the Si/Al ratio of the starting material prior to the nucleation and crystallization of zeolite. The adjustment of the Si/Al ratio of fly ash by addition of Na2SiO4 and Al(OH)(3) changed the type and CEC of zeolite. Waste solutions contained large amount of Si and little Al due to the formation of a zeolite named NaP1 in zeolite terminology with the Joint Committee of Powder Diffraction Standard (JCPDS) code of 39-0219. The alkalinity decreased largely. As a result, the CEC value of zeolite products synthesized with waste solution as alkali source decreased. The supplementation of new alkali to adjust the alkalinity of waste solution could enhance the CEC of synthesized product. It was concluded that: (1) addition of sodium halide and adjustment of the Si/Al ratio prior to synthesis can improve the quality of zeolite; (2) waste solutions produced following the zeolitization of fly ash can be reused as an alkali source in the activation of fly ash; zero-emission of waste solution in the synthesis of zeolite from fly ash is possible. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:266 / 272
页数:7
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