Engineered microwave biochar from sago bark waste for heavy metals adsorption

被引:9
作者
Wahi, R. [1 ]
Zuhaidi, N. F. Q. [1 ]
Yahaya, S. A. [1 ]
Lam, S. S. [2 ]
Imran-Shaukat, M. [1 ]
Aziz, S. M. A. [3 ]
Ngaini, Z. [1 ]
Pauzan, A. S. Mohamad [1 ]
机构
[1] Univ Malaysia Sarawak, Fac Resource Sci & Technol, Kota Samarahan 94300, Sarawak, Malaysia
[2] Univ Malaysia Terengganu, Sch Ocean Engn, Pyrolysis Technol Res Grp, Eastern Corridor Renewable Energy Grp, Kuala Terengganu 21030, Terengganu, Malaysia
[3] Univ Malaysia Sarawak, Ctr Preuniv Studies, Kuala Terengganu 94300, Sarawak, Malaysia
关键词
Microwave pyrolysis; Sago bark; Biochar; Heavy metal; Wastewater; AQUEOUS-SOLUTION; METHYLENE-BLUE; REMOVAL; PYROLYSIS; OPTIMIZATION; CADMIUM; WATER; SWITCHGRASS; BIOMASS; CARBON;
D O I
10.1016/j.matpr.2022.03.270
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Microwave pyrolysis is an energy, time, and cost-saving process for conversion of biowaste from agricultural sector into biochar. Sago bark waste was microwave pyrolyzed at 400 degrees C to produce sago bark microwave biochar (M-B), which was then treated with NaOH and HCl to generate acid-base modified sago bark microwave biochar (M-Bab). FTIR analysis evidenced the changes in functional groups in M-B and M-Bab. SEM analysis found that microwave pyrolysis resulted in the formation of open structures and pores on the M-B and acid-base modification increased the porous structure in M-Bab. BET surface area increased from 29.547 m(2)/g of (M-B) to 119.040 m(2)/g of (M-Bab) after acid-base modification. M-Bab demonstrated higher removal at low initial heavy metal concentrations in batch experiments. Best model to illustrate Cr (III), Ni (II), and Pb (II) adsorption by M-Bab best represented by Freundlich isotherm, while Cu (II) adsorption by Temkin isotherms. Conversion of sago bark waste to M-Bab is a potential solution for both water pollution remediation and the issue of sago bark waste overabundance. Copyright (C) 2021 Elsevier Ltd. All rights reserved. Selection and peer-review under responsibility of the scientific committee of the International Symposium of Reaction Engineering, Catalysis & Sustainable Energy.
引用
收藏
页码:1403 / 1414
页数:12
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