Characterisation of hexagonal birnessite with a new and rapid synthesis method-comparison with traditional synthesis

被引:4
|
作者
Qin, Zhangjie [1 ]
Chen, Xinmin [1 ]
Ouyang, Nanqi [1 ]
Lan, Shuai [1 ]
Jiang, Guanjie [1 ]
Zhang, Junxia [1 ]
Zhang, Qin [1 ]
机构
[1] Jiangxi Agr Univ, Coll Land Resource & Environm, Key Lab Poyang Lake Basin Agr Resource & Ecol Jia, Nanchang 330045, Jiangxi, Peoples R China
关键词
MANGANESE OXIDES; OXIDATION-STATE; CRYPTOMELANE; DISSOLUTION; MECHANISMS; ACID; PB2+; CRYSTALLIZATION; ADSORPTION; REACTIVITY;
D O I
10.1039/c9ra03332g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Birnessite is one of the most important manganese oxides that can control the geochemical behaviors of pollutants or can be applied to form industrial products. Many studies have been conducted on the synthesis of hexagonal birnessite because different synthesis methods can affect the structural, morphological, and physicochemical properties of hexagonal birnessite. However, there are still some defects in these synthesis methods. Therefore, a new synthesis method that is rapid, simple, and low-cost was proposed in this study involving the reduction of KMnO4 by H2O2 in a H2SO4 solution without controlling the pH, temperature and pressure. Using a series of XRD, chemical composition, AOS, SSA, SEM, FTIR, and TGA analyses, Bir-H2O2 was found to have lower crystallinity than Bir-HCl. However, the AOS and SSA of Bir-H2O2 were 3.87 and 103 m(2) g(-1) higher than those of Bir-HCl, i.e., 3.70 and 22 m(2) g(-1), respectively. Moreover, both Bir-H2O2 and Bir-HCl had similar particle morphology and thermal stability; in addition, the maximum adsorption content of Pb2+ on Bir-H2O2 (similar to 3006 mmol kg(-1)) was similar to 30% greater than that on Bir-HCl (similar to 2285 mmol kg(-1)) at pH 5.5; this indicated that the adsorption of Pb2+ on Bir-H2O2 was better and belonged to a pseudo-second-order model. All the abovementioned results indicate that Bir-H2O2 synthesized herein using the proposed synthesis method can have large application value.
引用
收藏
页码:25951 / 25956
页数:6
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