Carbonation processes in municipal solid waste incinerator bottom ash and their effect on the leaching of copper and molybdenum

被引:151
作者
Meima, JA
van der Weijden, RD
Eighmy, TT
Comans, RNJ
机构
[1] Energy Res Ctr Netherlands, ECN, NL-1755 ZG Petten, Netherlands
[2] Univ New Hampshire, Environm Res Grp, Durham, NH 03824 USA
[3] Delft Univ Technol, NL-26285 RX Delft, Netherlands
[4] Tech Univ Braunschweig, Dept Biochem Engn, D-38106 Braunschweig, Germany
关键词
D O I
10.1016/S0883-2927(02)00015-X
中图分类号
P3 [地球物理学]; P59 [地球化学];
学科分类号
0708 ; 070902 ;
摘要
The interaction of CO(2) with municipal solid waste incinerator (MSWI) bottom ash was studied in order to investigate the resulting changes in pH and bottom ash mineralogy and the impact that these changes have on the mobility of Cu and Mo. Carefully controlled carbonation experiments were performed on bottom ash suspensions and on filtered bottom ash leachates. Changes in leachate composition were interpreted with the geochemical model MINTEQA2, and neoformed minerals were investigated by means of chemical and spectroscopic analysis. The leaching of Cu and Mo during artificial carbonation is compared to the leachability of Cu and Mo from a sample of naturally carbonated bottom ash from the same incinerator. During carbonation in the laboratory, a precipitate was formed that consisted mainly of Al-rich amorphous material, calcite, and possibly gibbsite. Carbonation to pH approximate to8.3 resulted in a reduction of more than 50% in Cu leaching, and a reduction of less than 3% in Mo leaching. The reduction in Cu leaching is attributed to sorption to the neoformed amorphous Al-minerals. During natural weathering/carbonation of bottom ash, additional sorption sites are formed which further reduce the leaching of Cu and Mo on a time scale of months to years. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:1503 / 1513
页数:11
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