Novel and sustainable precursor for high-quality activated carbon preparation by conventional pyrolysis: Optimization of produce conditions and feasibility in adsorption studies

被引:15
作者
Saygili, Hasan [1 ]
Guzel, Fuat [2 ]
机构
[1] Batman Univ, Fac Engn & Architecture, Dept Petr & Nat Gas Engn, TR-72100 Batman, Turkey
[2] Dicle Univ, Fac Educ, Dept Chem, TR-21280 Diyarbakir, Turkey
关键词
Carob processing residues; Activated carbon; Production optimization; Characterization; Dye adsorption; ZINC-CHLORIDE ACTIVATION; HIGH-SURFACE-AREA; PHOSPHORIC-ACID ACTIVATION; METHYLENE-BLUE ADSORPTION; OIL PALM SHELL; CHEMICAL ACTIVATION; POROUS CARBONS; AQUEOUS-SOLUTION; DYES ADSORPTION; KOH ACTIVATION;
D O I
10.1016/j.apt.2017.12.014
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
The purpose of this study is to produce powdered activated carbon under optimized conditions from a novel precursor, carob (Ceratonia siliqua L.) industrial processing residues, by zinc chloride (ZnCl2) chemical activation. The production influences of impregnation ratio (ZnCl2/precursor, g g(-1)), carbonization temperature, and carbonization duration on the some textural properties of produced carbons have been investigated and the best production conditions were determined. The optimum conditions resulted in an activated carbon with a carbon content of 58.95% and a yield of 48.83%, while the surface area of 1693 m(2) g(-1), with the total pore volume of 2.655 cm(3) g(-1), mesoporosity of 98.95% and average pore diameter of 6.70 nm. Its adsorptive performance was tested using methylene blue and metanil yellow dyes. The adsorption behaviors for both dyes were well described by the Langmuir isotherm model, showing a monolayer adsorption capacity of 597 mg g(-1) and 568 mg g(-1), respectively. The results indicate that optimal activated carbon could be employed as an efficient adsorbent for the removal of the basic and acidic dyes from effluents. (C) 2017 The Society of Powder Technology Japan. Published by Elsevier B.V. and The Society of Powder Technology Japan. All rights reserved.
引用
收藏
页码:726 / 736
页数:11
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