M. A. Shiriazar, E. Sepehr, Ramin Haji Maleki, H. Khodaverdiloo, F. Asadzadeh, B. Dovlati, Z. Rengel
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Batch experiments were used for the assessment of the kinetics, isotherms, and the effects of initial solution pH (4, 6, 8, and 10), ionic strength (0.01, 0.1, and 0.2 mol L−1), and co-occurring anions (carbonate and phosphate) on the arsenate removal. Scanning electron microscope images showed Mg/Fe-LDH were loaded on the biochar porous structure, and X-ray diffraction analysis affirmed the presence of crystalline LDH minerals in Mg/Fe-LDH-biochar. Surface modification of biochar by Mg/Fe-LDH increased the maximum arsenate adsorption capacity (3.6 mg g−1) ten times compared to unmodified biochar (0.35 mg g−1). Arsenate removal capacity increased from 4.2 % to 54.2 % with modification of biochar by Mg/Fe-based LDH. Kinetic studies indicated that >90 % of Mg/Fe-LDH-biochar arsenate adsorption from a starting concentration of 10 mg L−1 occurred in the first 120 min. Pseudo-second order and Langmuir models described well the kinetics and isotherm of arsenate adsorption by biochar and Mg/Fe-LDH-biochar. Mg/Fe-LDH-biochar showed maximum arsenate removal capacity at pH 6. Increasing solution ionic strength and the presence of phosphate and carbonate anions suppressed arsenate removal by Mg/Fe-LDH-biochar. 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引用次数: 1
摘要
由于世界上许多国家的水源受到砷污染,需要开发无毒廉价的除砷材料。本研究的主要目的是表征Mg/Fe层状双氢氧化物/生物炭[镁/铁层状双氢氧化物(Mg/Fe- ldh)]复合材料对溶液中砷酸盐的吸附能力和行为。在限氧气氛下,500℃条件下,利用苹果剪枝残渣制备生物炭。采用原位共沉淀法合成了Mg/ fe - ldh生物炭。采用批量实验来评估动力学、等温线,以及初始溶液pH(4、6、8和10)、离子强度(0.01、0.1和0.2 mol L−1)和共生阴离子(碳酸盐和磷酸盐)对砷酸盐去除的影响。扫描电镜图像显示Mg/Fe-LDH被加载在生物炭的多孔结构上,x射线衍射分析证实Mg/Fe-LDH-生物炭中存在结晶LDH矿物。Mg/Fe-LDH改性生物炭的最大砷酸盐吸附量(3.6 Mg g−1)是未改性生物炭(0.35 Mg g−1)的10倍。Mg/ fe基LDH对生物炭的砷酸盐去除率由4.2%提高到54.2%。动力学研究表明,当初始浓度为10 Mg L−1时,Mg/ fe - ldh -生物炭对砷酸盐的吸附在前120 min内达到bbb90 %。拟二级模型和Langmuir模型很好地描述了生物炭和Mg/ fe - ldh -生物炭吸附砷酸盐的动力学和等温线。Mg/ fe - ldh生物炭在pH为6时脱除砷酸盐的能力最大。增加溶液离子强度和磷酸盐和碳酸盐阴离子的存在抑制了Mg/ fe - ldh生物炭对砷酸盐的去除。总之,使用Mg/Fe-LDH对生物炭进行表面改性,产生了一种可能更具成本效益、可在当地获得、可重复使用且无毒的砷吸附剂,用于地表水和地下水的净化。
Arsenate removal from aqueous solutions by Mg/Fe-LDH-modified biochar derived from apple tree residues
ABSTRACT The development of non-toxic and inexpensive materials for arsenic removal is required due to water sources being polluted by arsenic in many countries around the world. The main aim of this study was to characterise the capacity and behaviour of Mg/Fe layered double hydroxides/biochar [Magnesium/Iron-Layered Double Hydroxide (Mg/Fe-LDH)] composite for arsenate adsorption from solution. Apple tree pruning residues were used to produce biochar at 500 °C under oxygen-limited atmosphere. Mg/Fe-LDH-biochar was synthesised using a spontaneous in situ co-precipitation method. Batch experiments were used for the assessment of the kinetics, isotherms, and the effects of initial solution pH (4, 6, 8, and 10), ionic strength (0.01, 0.1, and 0.2 mol L−1), and co-occurring anions (carbonate and phosphate) on the arsenate removal. Scanning electron microscope images showed Mg/Fe-LDH were loaded on the biochar porous structure, and X-ray diffraction analysis affirmed the presence of crystalline LDH minerals in Mg/Fe-LDH-biochar. Surface modification of biochar by Mg/Fe-LDH increased the maximum arsenate adsorption capacity (3.6 mg g−1) ten times compared to unmodified biochar (0.35 mg g−1). Arsenate removal capacity increased from 4.2 % to 54.2 % with modification of biochar by Mg/Fe-based LDH. Kinetic studies indicated that >90 % of Mg/Fe-LDH-biochar arsenate adsorption from a starting concentration of 10 mg L−1 occurred in the first 120 min. Pseudo-second order and Langmuir models described well the kinetics and isotherm of arsenate adsorption by biochar and Mg/Fe-LDH-biochar. Mg/Fe-LDH-biochar showed maximum arsenate removal capacity at pH 6. Increasing solution ionic strength and the presence of phosphate and carbonate anions suppressed arsenate removal by Mg/Fe-LDH-biochar. In summary, surface modification of biochar using Mg/Fe-LDH produced a potentially more cost-effective, locally available, reusable, and non-toxic arsenic adsorbent for decontamination of surface- and groundwater.
期刊介绍:
Earth and Environmental Science Transactions (formerly Transactions of the Royal Society of Edinburgh: Earth Sciences) is a general earth sciences journal publishing a comprehensive selection of substantial peer-reviewed research papers, reviews and short communications of international standard across the broad spectrum of the Earth and its surface environments. The journal prides itself on the quality of its graphics and photographic reproduction. The Editors are keen to encourage interdisciplinary papers and Transactions also publishes occasional special symposia and invited volumes of specific interest.
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