Soft-template solvent thermal method synthesis of magnetic mesoporous carbon-silica composite for adsorption of methyl orange from aqueous solution

被引:6
|
作者
Zhu, Bo [1 ]
Xu, Jiangyan [1 ]
Xu, Zhihui [1 ]
Wu, Meisheng [1 ]
Jiang, Hongmei [1 ]
机构
[1] Nanjing Agr Univ, Coll Sci, Weigang St 1, Nanjing 210095, Peoples R China
基金
中国国家自然科学基金;
关键词
Soft template; Solvent thermal method; Magnetic mesoporous carbon-silica composites; Methyl orange; Adsorption; Bo Zhu and Jiangyan Xu contributed equally to this paper; HIGHLY EFFECTIVE ADSORPTION; FACILE PREPARATION; NANOPARTICLE; REMOVAL; NANOCOMPOSITES; MICROSPHERES; BLUE;
D O I
10.1007/s11356-021-18135-5
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
A facile soft-template solvent thermal strategy was developed to prepare mesoporous carbon-silica composite (MMCS) by using furfuryl alcohol (FA) as carbon precursor, Pluronic copolymer P123 as template, hydrated iron nitrate as iron source, and teraethylorthosilicate as silicon source and it was applied for the removal of methyl orange (MO). The as-synthesized MMCS with abound of hydrophilic groups processed a high specific surface area, large pore volume, and good magnetic response. With the increased amount of FA, the surface area and functional groups increased, promoting the adsorption effect. The maximum adsorption capacity of MO on MMCS can be high to 113.1 mg g(-1) at pH 4 with 150 mg L-1 initial MO concentration. The adsorption isotherm, kinetic, and thermodynamics were all studied and the results showed the adsorption process well fitted Langmuir adsorption isotherm and pseudo-second-order model. Additionally, it was shown that the adsorption process could not be interfered by the co-existence of PO43-, NO3-, CO32-, SO42-, and real water matrix. And the proposed adsorbent can remove MO in three practical water samples with satisfied removal rates ranging from 92.8 to 99.8%. Thus, the MMCS prepared in this study could be utilized as an alternative adsorbent for the removal of methyl orange from practical aqueous solution.
引用
收藏
页码:40734 / 40744
页数:11
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