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Natural gas regeneration of carbonate melts following SO2 capture from non-ferrous smelter emissions

机译:从有色金属冶炼厂排放中捕获SO 2 后碳酸盐熔体的天然气再生

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Sulfur emission in the form of SO2 in flue gases is the one of the most serious atmospheric pollutants associated with coal combustion and non-ferrous metal production. The carbonate eutectic method for removing SO2 from flue gases at 723–923 K was initially proposed in the 1970's but despite its great efficiency (SO2 concentration in the flue gas after purification reached 0.003 vol%) it could not be implemented by industry due to the complexity of the carbonate melt regeneration stage. Earlier we proposed a method suited to coal-firing power stations where the melt was regenerated using CO as a reducing agent. However, most metallurgical plants do not use coal and therefore lack a large source of CO. Here we propose a method for removing sulfur from the carbonate eutectic melt by purging it with natural gas or a natural gas/air mixture, which are available in the vast majority of metallurgical plants. This reaction leads to the reduction of sulfate to H2S gas that leaves the melt. The experiments we conducted show that nearly complete sulfur removal from the melt is possible at 823 K and that the reaction rate is sufficiently high for a large scale process. The proposed modifications provide solutions to two major problems previously encountered: (i) high temperature corrosion of the reaction cell can be avoided, since a stainless steel cell with high chromium content is stable with respect to the carbonate eutectic melt at 823 K, and (ii) removal of sulfur in the form of H2S provides considerable freedom in choosing the final industrially useful product: either sulfuric acid, using H2S dry combustion, or elemental sulfur via the Claus process. One can foresee that this carbonate melt-based SO2 removal technique may become a practical and economically attractive method for limiting sulfur emission to the atmosphere from non-ferrous metallurgical processing plants.
机译:烟气中SO 2 形式的硫排放是与燃煤和有色金属生产相关的最严重的大气污染物之一。最初在1970年代提出了碳酸盐共晶法从723–923 K烟气中去除SO 2 的方法,但尽管效率很高(SO 2净化后烟气中的 浓度达到0.003 vol%),由于碳酸盐熔体再生阶段的复杂性,工业上无法实现。早先我们提出了一种适用于燃煤电厂的方法,在燃煤电厂中,使用CO作为还原剂对熔体进行再生。但是,大多数冶金厂不使用煤,因此缺乏大量的CO。在这里,我们提出了一种方法,可以通过用天然气或天然气/空气混合物吹扫碳酸盐共晶熔体中的硫来去除硫。绝大多数冶金厂。该反应导致硫酸盐还原为离开熔体的H 2 S气体。我们进行的实验表明,在823 K下可以从熔体中几乎完全脱除硫,并且对于大规模工艺而言,反应速率足够高。提出的修改方案为先前遇到的两个主要问题提供了解决方案:(i)可以避免反应池的高温腐蚀,因为高铬含量的不锈钢池对于823 K的碳酸盐共晶熔体是稳定的,和( ii)脱除H 2 S形式的硫为选择最终的工业有用产品提供了很大的自由度:使用H 2的硫酸 S干式燃烧,或者通过Claus过程的元素硫。可以预见,这种基于碳酸盐熔体的SO 2 去除技术可能成为限制有色冶金冶炼厂向大气排放硫的实用且经济上有吸引力的方法。

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