Krishna BS, Murty DS
Department of Chemistry, Bangalore Institute of Technology, K. R. Road, Bangalore, 560 004, India
J Colloid Interface Sci. 2000 Sep 1;229(1):230-236. doi: 10.1006/jcis.2000.7015.
Batch sorption experiments performed on Cr(VI) species sorption showed a significantly enhanced removal of inorganic hexavalent chromium anionic species from aqueous solution by montmorillonite clays modified with quaternary amine, hexadecyltrimethylammonium (HDTMA) bromide. Unmodified clay had no affinity for chromium(VI) species. The sorption of Cr(VI) species has been carried out as a function of pH, contact time, adsorbate concentration (4.14x10(-5) to 8.62x10(-3) M), and temperature (5-45 degrees C). The surfactant-modified clay surface was stable when exposed to extremes in pH. The optimum pH for maximum sorption of Cr(VI) species was found to be at pH 1 and was constant between pH 2 and pH 6. The sorption data obtained was well described by DKR and Langmuir sorption isotherms. Sorption energy (E) for (i) surfactant sorption by montmorillonite clay and (ii) sorption of chromium(VI) species by surfactant modified clay have been computed from the DKR equation. Sorption energy evaluated for the sorption of both surfactant and Cr(VI) species showed that an ion-exchange mechanism was operative. The mechanism of retention appears to be replacement of counterion of the surfactant by Cr(VI) anionic species. Adsorbent capacity for the sorption of Cr(VI) species has been evaluated from the Langmuir sorption isotherm data. Thermodynamic parameters (Delta H degrees, Delta S degrees and Delta G degrees ) for surfactant sorption on montmorillonite clay and Cr(VI) sorption by modified clay have been evaluated. The specific rate constant for sorption of Cr(VI) species on modified montmorillonite was rapid during the first 10 min and equilibrium was found to be attained within 30 min. The sorption of Cr(VI) species onto modified montmorillonite clay followed first-order rate kinetics. Copyright 2000 Academic Press.
对铬(VI)物种吸附进行的批量吸附实验表明,用季胺十六烷基三甲基溴化铵(HDTMA)改性的蒙脱石粘土能显著增强从水溶液中去除无机六价铬阴离子物种的能力。未改性的粘土对铬(VI)物种没有亲和力。铬(VI)物种的吸附是作为pH值、接触时间、吸附质浓度(4.14×10⁻⁵至8.62×10⁻³ M)和温度(5 - 45℃)的函数进行的。当暴露于极端pH值时,表面活性剂改性的粘土表面是稳定的。发现铬(VI)物种最大吸附的最佳pH值为pH 1,并且在pH 2至pH 6之间保持恒定。获得的吸附数据用DKR和朗缪尔吸附等温线很好地描述。已根据DKR方程计算了(i)蒙脱石粘土对表面活性剂的吸附和(ii)表面活性剂改性粘土对铬(VI)物种的吸附的吸附能(E)。对表面活性剂和铬(VI)物种吸附评估的吸附能表明离子交换机制起作用。保留机制似乎是铬(VI)阴离子物种取代表面活性剂的抗衡离子。已根据朗缪尔吸附等温线数据评估了吸附剂对铬(VI)物种的吸附容量。评估了表面活性剂在蒙脱石粘土上的吸附以及改性粘土对铬(VI)的吸附的热力学参数(ΔH°、ΔS°和ΔG°)。铬(VI)物种在改性蒙脱石上的吸附在最初10分钟内速率很快,并且在30分钟内达到平衡。铬(VI)物种在改性蒙脱石粘土上的吸附遵循一级速率动力学。版权所有2000年学术出版社。