In situ ESEM study of the thermal decomposition of chrysotile asbestos in view of safe recycling of the transformation product

被引:40
作者
Gualtieri, Alessandro F. [1 ]
Gualtieri, Magdalena Lassinantti [2 ]
Tonelli, Massimo [3 ]
机构
[1] Univ Modena & Reggio Emilia, Dipartimento Sci Terra, I-41100 Modena, Italy
[2] Univ Modena & Reggio Emilia, Dipartimento Fis, I-41100 Modena, Italy
[3] Univ Modena & Reggio Emilia, Ctr Interdipartimentale Grandi Strumenti, I-41100 Modena, Italy
关键词
asbestos; chrysotile; in situ ESEM; cement-asbestos; dehydroxylation; pressure;
D O I
10.1016/j.jhazmat.2007.12.016
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The thermal transformation of asbestos into non-hazardous crystalline phases and their recycling is a promising solution for the "asbestos problem". The most common asbestos-containing industrial material produced worldwide is cement-asbestos. Knowledge of the kinetics of thermal transformation of asbestos fibers in cement-asbestos is of paramount importance for the optimization of the firing process at industrial scale. Here, environmental scanning electron microscopy (ESEM) was used for the first time to follow in situ the thermal transformation of chrysotile fibers present in cement-asbestos. It was found that the reaction kinetics of thermal transformation of chrysotile was highly slowed down in the presence of water vapor in the experimental chamber with respect to He. This was explained by chemisorbed water on the surface of the fibers which affected the dehydroxylation reaction and consequently the recrystallization into Mg-silicates. In the attempt to investigate alternative and faster firing routes for the decomposition of asbestos, a low melting glass was mixed with cement-asbestos and studied in situ to assess to which extent the decomposition of asbestos is favored. It was found that the addition of a low melting glass to cement-asbestos greatly improved the decomposition reaction and decreased the transformation temperatures. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:260 / 266
页数:7
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