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Hybrid materials in the remediation of arsenic contaminated waters: a physico-chemical study

机译:混合材料在砷污染水的修复中的物理化学研究

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Hybrid materials are obtained by the organic modification of sericite using the organic cations viz. tetramethylammonium chloride (TMA or T) and dimethyldioctadecylammonium chloride as (DDDMA or D) by a simple wet cation exchange process. Surface morphology of these solids is discussed with the Scanning Electron Microscopic images. Moreover, the materials are characterized by the X-ray diffraction and Fourier Transform-Infrared analytical techniques. Removal behavior of these organo-modified sericite samples is assessed for arsenite and arsenate from aqueous solutions under the batch and column reactor operations. The batch reactor experiments show that increasing the sorptive concentration (1-20mg/L) and pH (2-10) is caused to decrease the percent uptake of arsenite and arsenate significantly. Increasing the background electrolyte concentrations from 0.0001 to 0.1mol/L NaNO3 causes a significant decrease in percent removal of As(III) which infers that As(III) is sorbed onto the solid surface, primarily, by weak electrostatic or by van der Waals forces hence, forming an outer-sphere complexes at the solid surface. On the other hand As(V) uptake is insignificantly affected in presence of background electrolyte concentrations. This indicates that As(V) is sorbed by a strong chemical force and forming an inner sphere complexes onto the solid surface. The equilibrium state modeling shows that the data is fitted well to the Freundlich and Langmuir adsorption isotherms. The sorption capacities of these solids are calculated under these equilibrium conditions which indicate that organo-modified-sericite samples possess significantly higher removal capacity comparing to the virgin sericite. The leaching of the organic molecules (T or D) are also conducted in the sorption process of As(III) or As(V) and shows that almost negligible amount of T or D leaches in the bulk solutions since the Total Organic Carbon value of the bulk solution is not increased. Further, the breakthrough curves are obtained for these oxyanions under the column experimentations and the data is fitted well to the Thomas equation hence, the maximum loading capacity for arsenic is estimated under the dynamic conditions.
机译:杂化材料是通过使用有机阳离子对绢云母进行有机改性而获得的。四甲基氯化铵(TMA或T)和二甲基二十八烷基氯化铵(DDDMA或D)是通过简单的湿阳离子交换过程完成的。用扫描电子显微镜图像讨论了这些固体的表面形态。此外,这些材料的特征在于X射线衍射和傅里叶变换红外分析技术。在分批和塔式反应器操作下,评估了这些有机改性的绢云母样品的去除行为,以分析其从水溶液中的砷和砷酸盐。间歇反应器实验表明,增加吸附剂浓度(1-20mg / L)和pH(2-10)会导致砷和砷酸盐的摄取百分比显着降低。将背景电解质浓度从0.0001升至0.1mol / L NaNO3会导致As(III)去除百分率的显着降低,这表明主要由于弱静电或范德华力将As(III)吸附到固体表面上因此,在固体表面形成外球络合物。另一方面,在背景电解质浓度存在的情况下,对As(V)的吸收影响很小。这表明As(V)被强大的化学力吸收,并在固体表面上形成内球络合物。平衡状态模型表明,该数据非常适合Freundlich和Langmuir吸附等温线。在这些平衡条件下计算了这些固体的吸附能力,这表明有机改性的绢云母样品比纯绢云母具有明显更高的去除能力。在As(III)或As(V)的吸附过程中也进行了有机分子(T或D)的浸出,这表明本体溶液中T或D浸出的量几乎可以忽略不计,因为批量解决方案不会增加。此外,在柱实验中获得了这些含氧阴离子的穿透曲线,并且数据与托马斯方程非常吻合,因此,可以在动态条件下估算砷的最大负载量。

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