Xing Kun, Wang Hai-Zeng, Li Xiao-Yu
Key Laboratory of Marine Chemistry Theory and Technology, Ministry of Education, College of Chemistry and Chemical Engineering, Ocean University of China, Qingdao 266100, China.
Huan Jing Ke Xue. 2009 Mar 15;30(3):748-54.
The comparison of calcined Mg-Al layered double hydroxides (Mg-Al CLDH) for adsorption of arsenite and arsenate anions from aqueous solution was investigated by batch method. The results show that Mg-Al CLDH is an effective adsorbent for the removal of arsenite and arsenate anions. The adsorption processes are followed 'memory effect'. When the initial concentration of arsenic is lower than 10 mg x L(-1) for arsenite and 40 mg x L(-1) for arsenate, the equilibrium concentration of arsenic is lower than 10 microg x L(-1). In the range of 4-500 mg x L(-1) for initial arsenic concentration, the maximum adsorption capacity of arsenite and arsenate on Mg-Al CLDH from 298 to 323 K is 150.46-224.03 mg x g(-1) and 149.62-224.76 mg x g(-1), respectively, which are much larger than other adsorbents. But the adsorption capacity is not reached saturation, it is continued to increase significantly. L and H model can be used to describe the adsorption isotherm of arsenite and arsenate, respectively. The adsorption data are corresponded to the Freundlich model for arsenite and Langmuir model for arsenate at lower equilibrium concentration, but corresponded to Freundlich model for arsenite and arsenate at higher equilibrium concentration. Under the same temperature and initial concentration, the adsorption rate and removal rate of arsenate are higher than those of arsenite. And they are increased with temperate but decreased with increase in initial concentration. Adsorption processes follow the pseudo-second-order kinetic model for both arsenite and arsenate. The removal rate is not influenced by the initial pH (3.0-10.0). The adsorption capacity is influenced insignificantly by ionic strength. Arsenate anions are adsorbed firstly from arsenite and arsenate solution on Mg-Al CLDH.
采用分批法研究了煅烧镁铝层状双氢氧化物(Mg-Al CLDH)对水溶液中亚砷酸根和砷酸根阴离子的吸附性能。结果表明,Mg-Al CLDH是去除亚砷酸根和砷酸根阴离子的有效吸附剂。吸附过程呈现“记忆效应”。当亚砷酸根的初始砷浓度低于10 mg·L⁻¹且砷酸根的初始砷浓度低于40 mg·L⁻¹时,砷的平衡浓度低于10 μg·L⁻¹。在初始砷浓度为4 - 500 mg·L⁻¹范围内,298至323 K时亚砷酸根和砷酸根在Mg-Al CLDH上的最大吸附容量分别为150.46 - 224.03 mg·g⁻¹和149.62 - 224.76 mg·g⁻¹,远高于其他吸附剂。但吸附容量未达到饱和,仍继续显著增加。L模型和H模型可分别用于描述亚砷酸根和砷酸根的吸附等温线。在较低平衡浓度下,亚砷酸根的吸附数据符合Freundlich模型,砷酸根的吸附数据符合Langmuir模型;在较高平衡浓度下,亚砷酸根和砷酸根的吸附数据均符合Freundlich模型。在相同温度和初始浓度下,砷酸根的吸附速率和去除率高于亚砷酸根。它们随温度升高而增加,但随初始浓度增加而降低。亚砷酸根和砷酸根的吸附过程均遵循准二级动力学模型。去除率不受初始pH值(3.0 - 10.0)的影响。吸附容量受离子强度的影响不显著。在Mg-Al CLDH上,砷酸根阴离子优先从亚砷酸根和砷酸根溶液中被吸附。