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腐植酸对水体中五价钒的吸附
引用本文:刘梦,王华静,王鲲鹏,杨金燕.腐植酸对水体中五价钒的吸附[J].农业环境科学学报,2016,35(5):969-975.
作者姓名:刘梦  王华静  王鲲鹏  杨金燕
作者单位:1. 四川师范大学地理与资源科学学院,成都 610101; 四川大学建筑与环境学院,成都 610065;2. 四川师范大学地理与资源科学学院,成都,610101;3. 四川大学建筑与环境学院,成都,610065
基金项目:四川师范大学研究生优秀论文培育基金(校研字[2015]5号-42);国家自然科学基金项目(41101484);科技部欧盟国际科技合作项目(2011DFA101222)
摘    要:采用批次实验法,研究了腐植酸浓度、钒离子浓度、吸附时间、温度、溶液p H、离子强度、电解质等对腐植酸吸附水体中五价钒的影响。结果表明,钒溶液浓度为90.91 mg·L~(-1)条件下,腐植酸的浓度为1.09 g·L~(-1)时,腐植酸对钒的吸附量最大。随着钒溶液浓度的增加,吸附率逐渐降低并趋于0;而吸附量呈增加-缓慢增加-平衡的趋势;在腐植酸浓度为1.09 g·L~(-1)条件下,钒溶液浓度为1 818.18 mg·L~(-1)时,吸附量达到最大值,吸附等温线与Langmuir模型基本吻合。随着溶液pH、温度的增加,腐植酸对钒的吸附量逐渐减少,即在酸性、温度较低的条件下更有利于腐植酸对钒的吸附。随着溶液电解质浓度的增加,腐植酸对钒的吸附量逐渐降低。红外光谱和扫描电镜的结果显示,腐植酸对钒的吸附机制为钒在腐植酸的表面和内部形成稳定的络合物,这与腐植酸的O-H(或N-H)的氢键、C-O和C-H键的伸缩振动有关。因此,可以考虑用适量的腐植酸作吸附剂,去除水体中的钒,并调整环境条件增强吸附效果。

关 键 词:腐植酸    吸附  影响因素
收稿时间:2015/11/19 0:00:00

Adsorption of pentavalent vanadium by humic acid in water
LIU Meng,WANG Hua-jing,WANG Kun-peng and YANG Jin-yan.Adsorption of pentavalent vanadium by humic acid in water[J].Journal of Agro-Environment Science( J. Agro-Environ. Sci.),2016,35(5):969-975.
Authors:LIU Meng  WANG Hua-jing  WANG Kun-peng and YANG Jin-yan
Institution:College of Geography and Resources Science, Sichuan Normal University, Chengdu 610101, China;College of Architecture and Environment, Sichuan University, Chengdu 610065, China,College of Geography and Resources Science, Sichuan Normal University, Chengdu 610101, China,College of Architecture and Environment, Sichuan University, Chengdu 610065, China and College of Architecture and Environment, Sichuan University, Chengdu 610065, China
Abstract:Vanadium(V)is released naturally and anthropogenically to the environment and becomes an important pollutant. This study is conducted to examine adsorption characteristics of pentavalent VV(Ⅴ)] as NaVO3 in water by humic acid under a series of initial V con-centrations, humic acid concentrations, adsorption time, solution pH, temperature, ionic strength, and electrolyte type and concentrations. Results showed that:(1)at 90.91 mg·L-1 V(Ⅴ), the highest adsorption capacity of V was found at 1.09 g·L-1 of humic acid concentration;(2)with increases of V(Ⅴ)initial concentrations in solution, the adsorption rate gradually decreased, whereas the adsorption amount in-creased and reached the maximum at 1 818.18 mg·L-1 at 1.09 g·L-1 of humic acid concentration. Adsorption isotherm of V by humic acid could be well described by Langmuir model; (3)increasing solution pH and temperature gradually reduced the adsorption amount of V by humic acid, indicating that low temperature and low pH favored V adsorption by humic acid; (4)increasing electrolyte concentrations sup-pressed the adsorption of V by humic acid; (5)infrared spectrum and scanning electron microscopy showed that V complex was formed on the surface and the inside of humic acid and that the stretching vibration of O-H or N-H, C-O and C-H might also played role in V ad-sorption. Therefore, appropriate amount of humic acid could be used to remove V in water under certain environmental conditions.
Keywords:humic acid  vanadium  adsorption  influencing factors
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