Co-regulating the pore structure and surface chemistry of sludge-based biochar for high–performance deodorization of gaseous dimethyl disulfide

被引:0
|
作者
Wu, Jiangli [1 ]
Wan, Shungang [2 ,4 ]
Yuan, Dan [2 ]
Yi, Siqin [2 ]
Zhou, Lincheng [3 ]
Sun, Lei [2 ,4 ]
机构
[1] College of Ecology, Hainan University, Haikou,570228, China
[2] School of Chemistry and Chemical Engineering, Hainan University, Haikou,570228, China
[3] College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou,730000, China
[4] Key Laboratory of Solid Waste Resource Utilization and Environmental Protection of Haikou City, Haikou,570228, China
基金
中国国家自然科学基金;
关键词
Adsorption - Isotherms - Microporosity - Monolayers - Pore size - Pore structure - Specific surface area - Sulfur compounds - Surface chemistry;
D O I
10.1016/j.chemosphere.2024.142992
中图分类号
学科分类号
摘要
A straightforward and eco-friendly preparation method for porous sludge biochar (SBA-3) was developed to deodorize gaseous dimethyl disulfide (DMDS) using ion exchange to adjust micropore structures coupled with carboxyl functionalization. Compared with the unmodified sludge biochar SBA-1 and SBA-2 treated with ion exchange, the pore size of SBA-3 decreased accompanied with increasing specific surface area and micropore volume. The Brunauer–Emmett–Teller (BET) specific surface area and micropore volume were 176.35 m2 g−1 and 0.0314 cm³ g−1, which were 2.02 and 1.71-fold larger than those of SBA-2, as well as 20.60 and 78.5-fold larger than those of SBA-1, respectively. Meanwhile, the amount of –COOH on the surface of SBA-3 increased from 0.425 to 1.123 mmol g−1, which was 2.64-fold larger than that of SBA-1. The adsorption behavior between DMDS and SBA-3 could be well described by the quasi-second-order kinetic model and Langmuir isotherm model. The maximum monolayer adsorption capacity was 35.12 mg g−1 at 303 K. Thermodynamic and DFT calculations indicated that the adsorption of DMDS on SBA-3 was exothermic with the deodorization mechanisms involving pore filling and chemisorption. © 2024 Elsevier Ltd
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