Sulfur Transformation in a South Australian Low-Rank Coal during pyrolysis

Dong-Ke Zhang, Marnie Telfer
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引用次数: 10

Abstract

Sulfur transformation during pyrolysis of a high sulfur low-rank coal from South Australia has been studied. Three experimental techniques covering a wide range of conditions, namely, temperature-programmed pyrolysis, fixed-bed pyrolysis, and fluidized-bed pyrolysis, have been employed to investigate the effect of pyrolysis conditions on the interactions between different forms of sulfur and mechanisms of sulfur evolution during coal pyrolysis. Both chemical analysis method following Australian Standards and SEM with an energy dispersive X-ray detector are used for sulfur analysis of the char. The results reveal that sulfur evolution is a net result of organic and inorganic sulfur decomposition and interaction. The presence and conversion of inorganic sulfur into complex organic sulfur compounds provide a major mechanism for sulfur retention in char during pyrolysis. The difference in heating rates in the different pyrolysis experiments does not change the natural of the sulfur transformations but affects the extent to which they occur. Faster heating rates do not necessarily imply greater sulfur evolution due to formation of complex organic sulfur. Coal samples pretreated by acid washing and Ca and Na ion exchange are also used to examine the role of inorganic matter in sulfur transformation. At low temperatures (<400°C) acid washing shows little effect on sulfur retention, but at higher temperatures, sulfur retention is greatly reduced. While Na ion exchange enhances sulfur retention compared to the acid washed coal particularly at high temperatures (>400°C), Ca ion exchange shows the opposite trend. An increase in sulfide formation in the Ca ion-exchanged coal at high temperatures is observed, indicating that organic sulfur decomposition is enhanced in the presence of Ca. The effect on sulfur retaining of potential reactions involving Ca ions with sulfur may be offset by the catalyzing influence of Ca ions on organic sulfur decomposition.

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南澳大利亚低阶煤热解过程中硫的转化
研究了南澳大利亚一种高硫低阶煤在热解过程中的硫转化。采用程序升温热解、固定床热解和流化床热解三种实验技术,研究了不同热解条件对煤热解过程中不同形态硫相互作用的影响以及硫的演化机理。采用澳大利亚标准的化学分析方法和带能量色散x射线探测器的扫描电镜对焦炭进行硫分析。结果表明,硫的演化是有机和无机硫分解和相互作用的净结果。无机硫的存在和转化为复杂的有机硫化合物是煤热解过程中硫保留的主要机制。不同热解实验中升温速率的差异不会改变硫转化的性质,但会影响硫转化的发生程度。由于复杂有机硫的形成,更快的加热速率并不一定意味着更大的硫演化。用酸洗和钙钠离子交换预处理的煤样考察了无机物在硫转化中的作用。在低温(400℃)下,酸洗对硫的保留作用不大,但在高温下,硫的保留作用大大降低。与酸洗煤相比,钠离子交换提高了硫的保留率,特别是在高温下(>400℃),而钙离子交换则表现出相反的趋势。观察到高温下钙交换煤中硫化物的形成增加,表明Ca的存在促进了有机硫的分解。Ca离子与硫的潜在反应对保硫的影响可能被Ca离子对有机硫分解的催化作用所抵消。
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