One-pot synthesis of spherical nanoscale zero-valent iron/biochar composites for efficient removal of Pb(ii)

被引:11
|
作者
Shi, Yunlong [1 ,3 ]
Yu, Changjiang [1 ,2 ,3 ]
Liu, Mengying [3 ]
Lin, Qiang [1 ,2 ,3 ]
Lei, Man [3 ]
Wang, Darun [3 ]
Yang, Mengwei [3 ]
Yang, Yuting [3 ]
Ma, Jian [1 ,2 ,3 ]
Jia, Zhengya [4 ]
机构
[1] Hainan Normal Univ, Coll Chem & Chem Engn, Key Lab Water Pollut Treatment & Resource Reuse H, 99 Longkunnan Rd, Haikou 571158, Hainan, Peoples R China
[2] Hainan Normal Univ, Coll Chem & Chem Engn, Key Lab Trop Med Resource Chem, Minist Educ, 99 Longkunnan Rd, Haikou 571158, Hainan, Peoples R China
[3] Hainan Normal Univ, Coll Chem & Chem Engn, Key Lab Nat Polymer Funct Mat Haikou City, 99 Longkunnan Rd, Haikou 571158, Hainan, Peoples R China
[4] Hainan Huantai Inspect Technol Co Ltd, Haikou 571158, Hainan, Peoples R China
基金
海南省自然科学基金;
关键词
AQUEOUS-SOLUTION; HEAVY-METALS; SODIUM ALGINATE; BIOCHAR; ADSORPTION; CARBON; PB2+; IRON; CR(VI); CARBONIZATION;
D O I
10.1039/d1ra07373g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In this study, a spherical Fe/C composite (AIBC) was successfully prepared via carbonization of Fe3+-crosslinked sodium alginate. The removal capacity and mechanism of AIBC were evaluated for the adsorption of Pb(ii) from aqueous solution and compared with that of commercial nanoscale zero-valent iron (nZVI). The effects of the initial concentration, pH of Pb(ii) solution, the contact time, coexisting anions, and aging under air were investigated. The results showed that the pH had a strong impact on the adsorption of Pb(ii) by AIBC. The adsorption data for AIBC followed the Langmuir model, while the maximum adsorption capacity at pH 5 was 1881.73 mg g(-1). The AIBC had a higher adsorption capability than nZVI, especially under the condition of relatively high Pb(ii) concentrations. The oxidation-reduction reaction between Fe and Pb(ii) was the main mechanism for the adsorption of Pb(ii) onto nZVI. AIBC converted the largest amount of Pb(ii) into PbO center dot XH2O/Pb(OH)(2) mainly by generating Fe2+.
引用
收藏
页码:36826 / 36835
页数:10
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