The role of Mn oxide doping in phosphate removal by Al-based bimetal oxides: adsorption behaviors and mechanisms

被引:33
作者
Wu, Kun [1 ,3 ]
Liu, Ting [2 ]
Ma, Chao [2 ]
Chang, Bing [2 ]
Chen, Rong [1 ,3 ]
Wang, Xiaochang [1 ,3 ]
机构
[1] Xian Univ Architecture & Technol, Sch Environm & Municipal Engn, Xian 710055, Peoples R China
[2] Northwest A&F Univ, Coll Resources & Environm, Xianyang 712100, Shaanxi, Peoples R China
[3] MOE, Key Lab Water Resource Environm & Ecol, Xian 710055, Peoples R China
基金
高等学校博士学科点专项科研基金; 中国博士后科学基金;
关键词
Bimetal; Adsorption; Al oxide; Mn oxide doped; Phosphate; PHOSPHORUS REMOVAL; AQUEOUS-SOLUTION; METAL-OXIDES; ADSORBENT; WATER; ARSENATE; FLUORIDE; SORPTION; WATER/WASTEWATER; REACTIVITY;
D O I
10.1007/s11356-013-1937-x
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
This study investigated the behaviors and mechanisms of phosphate adsorbed onto manganese (Mn) oxide-doped aluminum (Al) oxide (MODAO). The isotherm results demonstrated that the maximum amount of phosphorus (P) adsorbed onto MODAO was 59.8 mg/g at T = 298 K (pH 6.0). This value was nearly twice the amount of singular AlOOH and could increase with rising temperatures. The kinetic results illustrated that most of the P was adsorbed onto MODAO within 5 h, which was shorter than the equilibrium time of phosphate adsorption onto AlOOH. The Elovich model effectively described the adsorption kinetic data of MODAO because of its heterogeneous surface. The optimal solution pH for phosphate removal was approximately 5.0 because of electrostatic interaction effects. Meanwhile, the decrease in P uptake with increasing ion strength suggested that phosphate adsorption occurred through an outer-sphere complex. Phosphates would compete for adsorption sites on the surface of MODAO in the presence of fluoride ion or sulfate. In addition, the spectroscopic analysis results of Fourier transform infrared spectroscopy and X-ray photoemission spectroscopy indicated that removal mechanisms of phosphate primarily include adhesion to surface hydroxyl groups and ligand exchange.
引用
收藏
页码:620 / 630
页数:11
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