Metal retention in the solid residue after low-temperature pyrolysis of chromated copper arsenate (CCA)-treated wood

被引:21
|
作者
Helsen, L [1 ]
van den Bulck, E [1 ]
机构
[1] Katholieke Univ Leuven, Dept Mech Engn, B-3001 Heverlee, Leuven, Belgium
关键词
waste wood; CCA; copper; chromium; arsenic; treated wood; pyrolysis; metal analysis; zero release; pyrolysis residue; metal retention;
D O I
10.1089/109287503770736087
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Based on previous research work, it is expected that dry recuperation of the metals in chromated copper arsenate (CCA)-treated wood waste can be achieved by low-temperature pyrolysis if a combination of pyrolysis temperature and residence time can be found, for which the two requirements: (1) zero-emission of metals, and (2) metal agglomeration are satisfied. To determine the working conditions for zero metal release, pyrolysis experiments with precisely controlled temperature and residence time and accurately known input metal concentrations of the CCA-treated wood samples, were conducted. Temperatures lower than 327degreesC are considered, since the release of arsenic is thought to be controlled by the reduction reaction of As2O5 to AS(2)O(3), which occurs sharply at 327degreesC. Metal retentions are calculated based on the measured metal concentrations in the pyrolysis residue and in the dried CCA-treated wood. The results suggest that pyrolysis at 300degreesC for 20 min gives rise to zero release for the three metals (Cr, Cu, and AS), while pyrolysis at 320degreesC leads to nonnegligible metal releases. Thus, the experimental results suggest that the decomposition temperature of As2O5 is lower than 320degreesC. However, due to the high experimental uncertainty the observations are inconclusive. For future industrial applications, this study already shows that very careful control of process parameters will be required to ensure a zero arsenic emission. Moreover, this study indicates that an arsenic sampling and analysis method has to be developed and validated to be able to measure the arsenic emissions directly with high accuracy, instead of measuring metal retentions in the solid residue.
引用
收藏
页码:569 / 580
页数:12
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