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1.生态环境部南京环境科学研究所,江苏 南京 210042
2.河海大学环境学院,江苏 南京 210098
Received:20 January 2020,
Revised:2020-06-12,
Online First:03 November 2020,
Published:05 November 2020
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皋海岭, 徐斌, 高月香, 朱月明, 张松贺, 张毅敏. TiO2改性石墨烯电极电吸附去除污水中NH4+[J]. 化工学报, 2020, 71(11): 5309-5319 DOI: 10.11949/0438-1157.20200092.
GAO Hailing, XU Bin, GAO Yuexiang, ZHU Yueming, ZHANG Songhe, ZHANG Yimin. Removal of ammonium ions in wastewater by electrosorption with TiO2 modified graphene electrode[J]. CIESC Journal, 2020, 71(11): 5309-5319 DOI: 10.11949/0438-1157.20200092.
皋海岭, 徐斌, 高月香, 朱月明, 张松贺, 张毅敏. TiO2改性石墨烯电极电吸附去除污水中NH4+[J]. 化工学报, 2020, 71(11): 5309-5319 DOI: 10.11949/0438-1157.20200092. DOI:
GAO Hailing, XU Bin, GAO Yuexiang, ZHU Yueming, ZHANG Songhe, ZHANG Yimin. Removal of ammonium ions in wastewater by electrosorption with TiO2 modified graphene electrode[J]. CIESC Journal, 2020, 71(11): 5309-5319 DOI: 10.11949/0438-1157.20200092. DOI:
通过水热法制备得到TiO
2
改性石墨烯复合材料(RGO/TiO
2
),考察了其形貌结构和电化学性能。将其组装成电极,对比未改性石墨烯(RGO)电极和RGO/TiO
2
电极的电吸附NH
4
+
性能。重点考察外加电压、循环流速、初始浓度等工艺参数对RGO/TiO
2
电极电吸附NH
4
+
的影响,并对其电吸附NH
4
+
特性和对模拟实际含NH
4
+
废水深度脱NH
4
+
效果进行研究。结果表明:RGO/TiO
2
复合材料具有三维孔洞结构,比表面积为382.08 m
2
·g
-1
,比电容量在扫速为0.01 V·s
-1
时达到325.80 F·g
-1
,优于RGO材料。RGO/TiO
2
电极的初次电吸附量较RGO电极提升了28.3%,循环再生吸附10次后,RGO/TiO
2
电极的NH
4
+
吸附量仅降低了5.87%,循环再生吸附性能优于RGO电极。外加电压2.0 V、循环流速35 ml·min
-1
和NH
4
+
初始浓度1.0 mmol·L
-1
为RGO/TiO
2
电极的最佳NH
4
+
电吸附条件。RGO和RGO/TiO
2
电极电吸附NH
4
+
过程符合准一级动力学模型和Freundlich等温吸附模型,电吸附NH
4
+
为非均匀表面的多层吸附行为,以物理吸附为主。RGO/TiO
2
电极4级串联时对模拟实际含NH
4
+
炼油净化水的去除率达到86.84%。
In this study
the TiO
2
modified graphene composite material (RGO/ TiO
2
) was prepared by hydrothermal method
and its morphological structure and electrochemical properties were investigated. Then RGO/TiO
2
material was assembled into electrode
and NH
4
+
ions electrosorption efficiencies of unmodified graphene (RGO) electrode and the RGO/TiO
2
electrode were compared. The effects of applied voltage
circulating velocity and initial concentration on NH
4
+
ions electrosorption by RGO/TiO
2
electrode were investigated. The characteristics of NH
4
+
ions electrosorption and the effect of advanced NH
4
+
ions removal from simulated actual wastewater containing NH
4
+
ions were also studied. The results showed that the RGO/TiO
2
composite material had a three-dimensional pore structure with specific surface area of 382.08 m
2
·g
-1
and specific capacitance of 325.80 F·g
-1
at a scan rate of 0.01 V·s
-1
which were better than those of the RGO material. The initial adsorption capacity of RGO/TiO
2
electrode was 28.3% higher than that of RGO electrode. After 10 cycles of regeneration adsorption
the adsorption capacity of NH
4
+
ions of RGO/TiO
2
electrode only decreased 5.87%
and its cyclic regeneration adsorption property was better than that of RGO electrode. In addition
the applied voltage 2.0 V
circulating velocity 35 ml·min
-1
and initial concentration 1.0 mmol·L
-1
were the optimal NH
4
+
ions electrosorption conditions for RGO/TiO
2
electrode. The electrosorption process of NH
4
+
ions by RGO and RGO/TiO
2
electrodes was in accordance with the quasi-first-order kinetic model and the Freundlich isothermal adsorption model. The electrosorption of NH
4
+
ions was a multi-layer adsorption behavior on heterogeneous surface and physical adsorption was the dominant. When the RGO/TiO
2
electrode was connected in 4-stage series
the removal efficiency of simulated actual NH
4
+
refining purified water reached 86.84%.
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