The University of Texas at Austin, Department of Civil, Architectural, and Environmental Engineering, Austin, Texas 78712, USA.
Environ Sci Technol. 2009 Oct 15;43(20):7837-42. doi: 10.1021/es900991n.
Natural organic matter (NOM) removal during water softening is thought to occur through adsorption onto or coprecipitation with calcium and magnesium solids. However, details of precipitate composition and surface chemistry and subsequent interactions with NOM are relatively unknown. In this study, zeta potentiometry analyses of precipitates formed from inorganic solutions under varying conditions (e.g., Ca-only, Mg-only, Ca + Mg, increasing lime or NaOH dose) indicated that both CaCO3 and Mg(OH)2 were positively charged at higher lime (Ca(OH)2) and NaOH doses (associated with pH values above 11.5), potentially yielding a greater affinity for adsorbing negatively charged organic molecules. Environmental scanning electron microscopy (ESEM) images of CaCO3 solids illustrated the rhombohedral shape characteristic of calcite. In the presence of increasing concentrations of magnesium, the CaCO3 rhombs shifted to more elongated crystals. The CaCO3 solids also exhibited increasingly positive surface charge from Mg incorporation into the crystal lattice, potentially creating more favorable conditions for adsorption of organic matter. NOM adsorption experiments using humic substances extracted from Lake Austin and Missouri River water elucidated the role of surface charge and surface area on adsorption.
在水软化过程中,天然有机物 (NOM) 的去除被认为是通过与钙和镁固体的吸附或共沉淀发生的。然而,沉淀物的组成、表面化学性质以及随后与 NOM 的相互作用的细节相对未知。在这项研究中,通过动电电势分析,研究了在不同条件下(例如仅 Ca、仅 Mg、Ca+Mg、增加石灰或 NaOH 剂量)从无机溶液中形成的沉淀物,结果表明,在较高的石灰(Ca(OH)2)和 NaOH 剂量(与 pH 值高于 11.5 相关)下,CaCO3 和 Mg(OH)2 均带正电荷,可能对吸附带负电荷的有机分子具有更大的亲和力。CaCO3 固体的环境扫描电子显微镜 (ESEM) 图像说明了方解石的菱面体形状特征。随着镁浓度的增加,CaCO3 菱面体转变为更细长的晶体。由于镁掺入晶格,CaCO3 固体的表面电荷也越来越正,这可能为有机物的吸附创造了更有利的条件。使用从奥斯汀湖和密苏里河水中提取的腐殖质进行的 NOM 吸附实验阐明了表面电荷和表面积对吸附的作用。