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磁性Mg/Al-LDHs制备条件对其吸附除磷性能的影响
引用本文:李嘉雯,郝瑞霞,李宏康,王丽沙,刘思远,李鹏,孙彤,武旭源.磁性Mg/Al-LDHs制备条件对其吸附除磷性能的影响[J].环境科学学报,2020,40(2):520-526.
作者姓名:李嘉雯  郝瑞霞  李宏康  王丽沙  刘思远  李鹏  孙彤  武旭源
作者单位:北京工业大学,北京市水质科学与水环境恢复工程重点实验室,北京100124,北京工业大学,北京市水质科学与水环境恢复工程重点实验室,北京100124,北京工业大学,北京市水质科学与水环境恢复工程重点实验室,北京100124,北京工业大学,北京市水质科学与水环境恢复工程重点实验室,北京100124,北京工业大学,北京市水质科学与水环境恢复工程重点实验室,北京100124,北京工业大学,北京市水质科学与水环境恢复工程重点实验室,北京100124,北京工业大学,北京市水质科学与水环境恢复工程重点实验室,北京100124,北京工业大学,北京市水质科学与水环境恢复工程重点实验室,北京100124
基金项目:国家自然科学基金(No.51778011)
摘    要:为提高粉末状水滑石吸附剂的工程应用性,采用共沉淀法制备了磁性Mg/Al水滑石(Layered Double Hydroxides,LDHs).结合XRD、FTIR、SEM及VSM等材料表征结果,考察了制备条件(磁基质投加量、金属物质的量比和层间阴离子)对其吸附除磷性能、磁学性能及结构特征的影响.结果表明,在Fe_3O_4与Mg~(2+)物质的量比为0.02、Mg/Al物质的量比为2∶1和层间阴离子为Cl~-/OH~-的条件下制备出的磁性Mg/Al-LDHs对TP吸附性能最好,平衡吸附量可达49.60 mg·g~(-1);比饱和磁化强度为2.78 emu·g~(-1),能够实现吸附剂的快速高效磁分离回收.层间阴离子种类对水滑石焙烧前后吸附除磷性能有一定的影响:经高温焙烧后,层间含有CO■的水滑石吸磷能力虽有所提高,但仍低于无CO■型LDHs.因此,在水滑石制备过程中避免使用碳酸盐作为共沉碱原料,这样无需焙烧即可获得较高吸磷能力的吸附剂.

关 键 词:磁性Mg/Al-LDHs  吸附  磷酸根
收稿时间:2019/8/3 0:00:00
修稿时间:2019/11/3 0:00:00

Adsorption performance of phosphorus by magnetic Mg/Al-LDHs prepared under different conditions
LI Jiawen,HAO Ruixi,LI Hongkang,WANG Lish,LIU Siyuan,LI Peng,SUN Tong and WU Xuyuan.Adsorption performance of phosphorus by magnetic Mg/Al-LDHs prepared under different conditions[J].Acta Scientiae Circumstantiae,2020,40(2):520-526.
Authors:LI Jiawen  HAO Ruixi  LI Hongkang  WANG Lish  LIU Siyuan  LI Peng  SUN Tong and WU Xuyuan
Institution:Key Laboratory of Beijing for Water Quality Science and Water Environment Recovery Engineering, Beijing University of Technology, Beijing 100124,Key Laboratory of Beijing for Water Quality Science and Water Environment Recovery Engineering, Beijing University of Technology, Beijing 100124,Key Laboratory of Beijing for Water Quality Science and Water Environment Recovery Engineering, Beijing University of Technology, Beijing 100124,Key Laboratory of Beijing for Water Quality Science and Water Environment Recovery Engineering, Beijing University of Technology, Beijing 100124,Key Laboratory of Beijing for Water Quality Science and Water Environment Recovery Engineering, Beijing University of Technology, Beijing 100124,Key Laboratory of Beijing for Water Quality Science and Water Environment Recovery Engineering, Beijing University of Technology, Beijing 100124,Key Laboratory of Beijing for Water Quality Science and Water Environment Recovery Engineering, Beijing University of Technology, Beijing 100124 and Key Laboratory of Beijing for Water Quality Science and Water Environment Recovery Engineering, Beijing University of Technology, Beijing 100124
Abstract:In order to enhance the engineering application of powdered hydrotalcite adsorbents, magnetic Mg/Al hydrotalcites (layered double hydroxides, Mg/Al-LDHs) were prepared using co-precipitation method. Combined with the results of XRD, FTIR, SEM and VSM, the effects of Mg/Al-LDHs'' preparation conditions (magnetic matrix dosage, metal molar ratio and interlayer anion) on their phosphorus adsorption, magnetic properties and structural characteristics were investigated. The results show that the magnetic Mg/Al-LDHs prepared with the molar ratio of Fe3O4 to Mg2+ at 0.02, Mg/Al molar ratio at 2:1 and an interlayer anions of Cl-/OH- had the optimal adsorption performance to total phosphorus (TP), with an equilibrium adsorption capacity reaching 49.60 mg·g-1, while their specific saturation magnetization intensity reached 2.78 emu·g-1, which enabled rapid and efficient magnetic separation and recovery of adsorbent. It is found that the interlayer anions had a certain influence on the phosphorus adsorption by hydrotalcites before and after calcination. After calcination, the phosphorus absorption capacity of hydrotalcites containing CO32- in the interlayer improved, but is still lower than that of LDHs without CO32-. Therefore, in the preparation of hydrotalcites, carbonate should not be used as the raw material of co-precipitation alkali, so that the adsorbent with high phosphorus absorption ability could be obtained without calcination.
Keywords:magnetic Mg/Al-LDHs  adsorption  phosphorus
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