Studies on the oxidation reaction of L-cysteine in a confined matrix of layered double hydroxides

被引:19
|
作者
Chen, Qiuhua [1 ]
Shi, Shuxian [1 ]
Liu, Xiaolei [1 ,2 ]
Jin, Lan [1 ]
Wei, Min [1 ]
机构
[1] Beijing Univ Chem Technol, State Key Lab Chem Resource Engn, Beijing 100029, Peoples R China
[2] Zibo Vocat Inst, Dept Chem Engn, Zibo 255314, Peoples R China
基金
中国国家自然科学基金;
关键词
L-Cysteine; Confined reaction; Layered double hydroxide (LDH); Kinetic; AQUEOUS-SOLUTIONS; ACTIVE COMPOUNDS; INTERCALATION; HYDROTALCITE; REMOVAL; IRON; CHROMIUM(VI); CATALYSTS; KINETICS; SORPTION;
D O I
10.1016/j.cej.2009.06.034
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The amino acid L-cysteine (L-Cys) was intercalated into a MgAl layered double hydroxide (LDH). and its oxidation reaction by hexacyanoferrate (III) (Fe(CN)(6)(3-)) in the confined region between sheets of LDH has been studied in detail. Based on the measurement results of XRD, Raman and FT-IR, it was found that the interlayer L-Cys was oxidized to cystine by Fe(CN)(6)(3-). Furthermore, the kinetics of this reaction was investigated in batch mode. The influences of initial Fe(CN)(6)(3-) concentration, L-Cys-LDH quantity and reaction temperature on the interlayer oxidation reaction have been studied, respectively. The reaction follows a diffusion-controlled mechanism represented by Crank-Ginstling and Brounshtein kinetic model with the apparent activation energy of 29.93 kJ/mol. Therefore, this layered material may have prospective application as a novel "molecular reactor" for confined chemical reactions. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:175 / 182
页数:8
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