The effect of cysteine on the adsorption of Cd(II) by kaolinite was examined at 25 jC using a low-defect kaolinite fromMinas Gerais (Brazil) and a high-defect kaolinite from Berici Hills (Italy). The chemical data demonstrated that the amount ofCd–cysteine detected on kaolinite increases rapidly during the first few hours with a first-order reaction, thereafter adsorptionbecomes linear with time for low-defect kaolinite and slows rapidly for high-defect kaolinite. In low-ordered kaolinite, the Cd–cysteine is intercalated in the structure. Evidence of these changes was also observed by differential thermal analysis (DTA).The thermal decomposition of the Cd–cysteine adsorbed on the kaolinites was studied by analysing the evolved gases. Themass spectra of both samples show the evolution of NO (or CH3CH3, m/z = 30), CO2 (m/z = 44), and SO2 (m/z = 64) between 150 and 300 jC and of H2O (m/z = 18), CO2 (m/z = 44) and SO2 (m/z = 64) in the temperature range between 400 and 700 jC.The high-defect kaolinite also caused the evolution of molecular units with m/z=34 (H2S) and m/z=76 (N2O3). D 2002Elsevier Science B.V. All rights reserved.
Sorption of Cd-cysteine complexes by kaolinite / Benincasa, Emanuele; Brigatti, Maria Franca; Malferrari, Daniele; L., Medici; Poppi, Luciano. - In: APPLIED CLAY SCIENCE. - ISSN 0169-1317. - STAMPA. - 21:3-4(2002), pp. 191-201. [10.1016/S0169-1317(01)00100-4]
Sorption of Cd-cysteine complexes by kaolinite
BENINCASA, Emanuele;BRIGATTI, Maria Franca;MALFERRARI, Daniele;POPPI, Luciano
2002
Abstract
The effect of cysteine on the adsorption of Cd(II) by kaolinite was examined at 25 jC using a low-defect kaolinite fromMinas Gerais (Brazil) and a high-defect kaolinite from Berici Hills (Italy). The chemical data demonstrated that the amount ofCd–cysteine detected on kaolinite increases rapidly during the first few hours with a first-order reaction, thereafter adsorptionbecomes linear with time for low-defect kaolinite and slows rapidly for high-defect kaolinite. In low-ordered kaolinite, the Cd–cysteine is intercalated in the structure. Evidence of these changes was also observed by differential thermal analysis (DTA).The thermal decomposition of the Cd–cysteine adsorbed on the kaolinites was studied by analysing the evolved gases. Themass spectra of both samples show the evolution of NO (or CH3CH3, m/z = 30), CO2 (m/z = 44), and SO2 (m/z = 64) between 150 and 300 jC and of H2O (m/z = 18), CO2 (m/z = 44) and SO2 (m/z = 64) in the temperature range between 400 and 700 jC.The high-defect kaolinite also caused the evolution of molecular units with m/z=34 (H2S) and m/z=76 (N2O3). D 2002Elsevier Science B.V. All rights reserved.File | Dimensione | Formato | |
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