Bonding mechanisms between aflatoxin B1 and smectite

被引:108
作者
Deng, Youjun [1 ]
Velazquez, Ana Luisa Barrientos [1 ]
Billes, Ferenc [2 ]
Dixon, Joe B. [1 ]
机构
[1] Texas A&M Univ, Dept Soil & Crop Sci, College Stn, TX 77843 USA
[2] Budapest Univ Technol & Econ, Dept Phys Chem & Mat Sci, H-1521 Budapest, Hungary
关键词
Aflatoxin B-1; Smectite; Ion-dipole interaction; H-bonding; Infrared; SODIUM-CALCIUM ALUMINOSILICATE; NOVASIL CLAY INTERVENTION; HIGH-RISK; CRYSTAL-STRUCTURES; ADSORPTION; GHANAIANS; MONTMORILLONITE; ELIMINATION; PREVENTION; REDUCTION;
D O I
10.1016/j.clay.2010.07.008
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Bentonites were used in aflatoxin-contaminated feeds and diets to reduce bioavailability of the mycotoxin. The objectives of this study were to test accessibility of smectite interlayer space to aflatoxin adsorption and to investigate bonding mechanisms between adsorbed aflatoxin B-1 molecules and smectite. The aflatoxin smectite complex had a basal spacing greater than 1.2 nm up to 400 degrees C, which suggests interlayer aflatoxin adsorption. The in-phase carbonyl-stretching band shifted from 1736 cm(-1) for monovalent cation (K or Na) to 1687 cm(-1) for heavy-metal (Ni or Cu) complexes. At nearly 100% humidity, the cations did not distinctly affect band positions of the adsorbed aflatoxin molecules. We concluded that, under dry conditions, major bonding between adsorbed aflatoxin B-1 and smectite was ion-dipole interactions and coordination between exchangeable cations and carbonyl groups. Under humid conditions, H-bonding between carbonyl groups and exchangeable-cation hydration-shell water was the dominant bonding force. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:92 / 98
页数:7
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