Islam Mohammad Z, Catalan Lionel J J, Yanful Ernest K
Department of Chemical Engineering, Lakehead University, 955 Oliver Road, Thunder Bay, Ontario, Canada P7B 5E1.
Environ Sci Technol. 2004 Mar 1;38(5):1561-8. doi: 10.1021/es034659r.
Crushed samples of stabilized/solidified (s/s) waste were leached at constant leachate pH in the pH range 4-7 with nitric acid solutions to evaluate the influence of remineralization on metal release. The s/s waste consisted of synthetic heavy-metal sludge containing 0.1 mol L(-1) copper nitrate, 0.1 mol L(-1) zinc nitrate, and 0.1 mol L(-1) lead nitrate mixed with ordinary Portland cement. Unleached and leached particles were characterized by scanning electron microscopy and energy-dispersive X-ray spectrometry. Two consecutive leaching fronts advancing from the surface of the particles toward the center were identified: the first front was associated with the dissolution of portlandite and partial reaction of the calcium silicate hydrate gel, while the second front was associated with the dissolution of calcium-aluminum hydroxy sulfates such as ettringite and monosulfate. At pH 4 and 5, a remineralization zone rich in heavy metals formed immediately behind the second leaching front. The shell extending from the remineralization zone to the surface of the particles was depleted in calcium, sulfate, and heavy metals. As a result of remineralization, heavy-metal releases to the leachate were reduced by factors ranging between 3.2 and 6.2 at pH 4 and between 74 and 193 at pH 5. At pH 6 and 7, remineralization of Pb and Zn occurred further behind the second leaching front and closer to the surface of the particles. The amount of heavy-metal release depended on both the leachate pH and the remineralization factor.
将稳定化/固化(s/s)废物的粉碎样品在4 - 7的恒定渗滤液pH值下用硝酸溶液进行浸出,以评估再矿化对金属释放的影响。该s/s废物由含有0.1 mol L(-1)硝酸铜、0.1 mol L(-1)硝酸锌和0.1 mol L(-1)硝酸铅的合成重金属污泥与普通硅酸盐水泥混合而成。通过扫描电子显微镜和能量色散X射线光谱法对未浸出和浸出后的颗粒进行表征。确定了从颗粒表面向中心推进的两个连续浸出前沿:第一个前沿与氢氧化钙的溶解和硅酸钙水合物凝胶的部分反应有关,而第二个前沿与钙铝羟基硫酸盐如钙矾石和单硫酸盐的溶解有关。在pH值为4和5时,在第二个浸出前沿后方立即形成了富含重金属的再矿化区。从再矿化区延伸到颗粒表面的壳层中钙、硫酸盐和重金属含量减少。由于再矿化,在pH值为4时,重金属向渗滤液中的释放减少了3.2至6.2倍,在pH值为5时减少了74至193倍。在pH值为6和7时,铅和锌的再矿化发生在第二个浸出前沿后方更远且更靠近颗粒表面的位置。重金属释放量取决于渗滤液pH值和再矿化系数。