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不同插层阴离子的MgAlFe层状双氢氧化物对水溶液中砷酸盐和氟化物同步吸附的对比研究

Comparative study on synchronous adsorption of arsenate and fluoride in aqueous solution onto MgAlFe-LDHs with different intercalating anions.

作者信息

Hongtao Lu, Shuxia Liu, Hua Zhang, Yanling Qiu, Daqiang Yin, Jianfu Zhao, Zhiliang Zhu

机构信息

State Key Laboratory of Pollution Control and Resource Reuse, Tongji University Shanghai 200092 China.

Postdoctoral Research Station, College of Civil Engineering, Tongji University Shanghai 200092 China.

出版信息

RSC Adv. 2018 Sep 27;8(58):33301-33313. doi: 10.1039/c8ra05968c. eCollection 2018 Sep 24.

Abstract

In this study, a series of MgAlFe-LDHs (Cl, NO , intercalation, and calcined products of a CO interlayer) was synthesized and used for adsorption of arsenate and fluoride in individual contaminants and coexisting pollutant systems. Effects of various factors such as initial pH of solution, dosage of materials, coexisting ions, contact time, and initial pollutant concentrations were evaluated. Experimental results showed that different intercalating anions had a significant effect on adsorption performance of arsenate and fluoride in water. The adsorption of arsenate and fluoride on MgAlFe-CLDH, MgAlFe-Cl-LDH or MgAlFe-NO-LDH can be described by different adsorption isotherm equations. During the simultaneous removal process, arsenate and fluoride competed for adsorption sites of the adsorbent materials, and the fluoride ions had advantages in the competitive adsorption on MgAlFe-Cl-LDH and MgAlFe-NO-LDH. MgAlFe-NO-LDH was used to adsorb arsenate and fluoride in coexisting pollution systems (the concentration of each pollutant was 2 mg L, the adsorbent dosage was 1.5 g L). The remaining arsenic concentration was reduced to less than 10 μg L and the remaining fluoride ion concentration to below 20 μg L which meets the World Health Organization's, EPA's and China's drinking water standards for arsenic and fluoride limits. A possible mechanism is discussed with support from further XRD, SEM, and XPS analysis of the materials after their adsorption.

摘要

在本研究中,合成了一系列MgAlFe-LDHs(Cl、NO 、插层产物以及CO 插层的煅烧产物),并将其用于单一污染物体系以及共存污染物体系中砷酸盐和氟化物的吸附。评估了溶液初始pH值、材料用量、共存离子、接触时间和初始污染物浓度等各种因素的影响。实验结果表明,不同的插层阴离子对水中砷酸盐和氟化物的吸附性能有显著影响。砷酸盐和氟化物在MgAlFe-CLDH、MgAlFe-Cl-LDH或MgAlFe-NO-LDH上的吸附可用不同的吸附等温线方程描述。在同时去除过程中,砷酸盐和氟化物竞争吸附剂材料的吸附位点,氟离子在MgAlFe-Cl-LDH和MgAlFe-NO-LDH的竞争吸附中具有优势。使用MgAlFe-NO-LDH吸附共存污染体系中的砷酸盐和氟化物(每种污染物浓度为2 mg/L,吸附剂用量为1.5 g/L)。剩余砷浓度降至10 μg/L以下,剩余氟离子浓度降至20 μg/L以下,符合世界卫生组织、美国环保署和中国饮用水中砷和氟的限量标准。吸附后通过对材料进行进一步的XRD、SEM和XPS分析,探讨了可能的作用机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bad/9086567/8980bb04d8b0/c8ra05968c-f1.jpg

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