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Mercury adsorption and re-emission inhibition from actual WFGD wastewater using sulfur-containing activated carbon

机译:使用含硫活性炭抑制实际WFGD废水中的汞吸附和再排放

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A series of batch experiments were conducted to obtain the optimal adsorption condition for removing aqueous Hg from actual lime-based wet flue gas desulfurization (WFGD) wastewater with sulfur-containing activated carbon (SAC). The experimental results showed that SAC1 had an average 0.32 mu g mg(-1) larger aqueous Hg adsorption capacity and 21% larger Hg removal than the CS2-treated SAC1 (i.e., SAC2) in all tested pH values, confirming that greater sulfur content associated with effective sulfur functional group (i.e., elemental S) caused the larger Hg adsorption capacity. Furthermore, as increasing pH from 4 to 7, the Hg adsorption capacity of SAC1 decreased by 22% (i.e., 0.27 mu g mg(-1)). The equilibrium Hg adsorption capacity was well fitted with linear and Freundlich adsorption isotherms. Kinetic simulations showed that both pseudo-second order and Elovich equations could well describe the chemisorption behavior of Hg to SAC1. Thermodynamic parameter calculation confirmed that Hg adsorption by SAC1 was thermodynamically spontaneous and exothermic. Re-emission of gaseous Hg markedly decreased by 88% as SO32- addition increased from 0 to 0.01 mM. Notably, by the addition of SAC1, zero re-emission of gaseous Hg was achieved. These experimental results confirm that the capture of aqueous Hg2+ and the inhibition of gaseous Hg-0 re-emission can be successfully and simultaneously achieved in actual WFGD wastewater via the addition of SAC.
机译:进行了一系列的分批实验,以获得从含硫活性炭(SAC)的实际石灰基湿法烟气脱硫(WFGD)废水中去除Hg的最佳吸附条件。实验结果表明,在所有测试的pH值中,SAC1比CS2处理的SAC1(即SAC2)平均具有0.32μgmg(-1)的更大的水合汞吸附容量和21%的较大汞去除率,从而证实了更高的硫含量与有效硫官能团(即元素S)相关的Hg吸附容量更大。此外,随着pH从4增加到7,SAC1的Hg吸附能力降低了22%(即0.27μgmg(-1))。平衡的Hg吸附容量与线性和Freundlich吸附等温线非常吻合。动力学模拟表明,伪二级方程和Elovich方程都可以很好地描述Hg对SAC1的化学吸附行为。热力学参数计算证实,SAC1对Hg的吸附是热力学自发的且放热的。随着SO32添加量从0增加到0.01 mM,气态Hg的再排放显着降低了88%。值得注意的是,通过添加SAC1,实现了气态Hg的零再排放。这些实验结果证实,通过添加SAC,可以在实际WFGD废水中成功并同时实现Hg2 +水溶液的捕获和Hg-0气态再排放的抑制。

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