壳聚糖/膨润土纳米复合材料对水中硝酸盐离子电位响应的初步研究

Moises Oviedo Mendoza, Erika Padilla Ortega, O. Arias de Fuentes, Y. Prokhorov, J. Gabriel Luna Barcenas
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引用次数: 7

摘要

这项工作的范围是获得并表征纳米生物复合材料作为离子选择电极(ISE)用于水中硝酸盐离子的测定。这种纳米复合材料是基于壳聚糖的插入,一种阳离子生物聚合物,在膨润土。采用离子交换法制备了壳聚糖/膨润土纳米复合材料。CS中的氨基在酸性溶液中可以质子化,取代粘土表面的层间阳离子。在制备过程的最后加入硝酸盐(II),阻断阳离子交换位点,增强对硝酸盐的电位响应。采用溶剂浇铸法制备壳聚糖/膨润土薄膜。利用x射线衍射(XRD)、x射线光电子能谱(XPS)和傅里叶变换红外光谱(FTIR)对纳米复合材料进行表征。这些研究证实了壳聚糖是由于NH3+基团与带负电荷的膨润土表面之间的静电吸引作用而嵌入膨润土层间距的。这些测量结果证实,存在逆转这种纳米复合材料的离子交换的可能性。电位测量使用Ag/AgCl参比电极和ISE,在石墨-环氧电极上沉积壳聚糖/膨润土膜作为工作电极。在2×10-4M和8×10-1M之间进行了线性拟合,近似于-54.6 mV/dec的纳恩斯斜率。根据分离溶液法(SSM)计算了对某些干扰离子的选择性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Chitosan/bentonite nanocomposite: Preliminary studies of its potentiometric response to nitrate ions in water
The scope of this work is to obtain and characterize a nanobiocomposite as Ion Selective Electrodes (ISE) for nitrate ion determination in water. This nanocomposite is based upon the intercalation of chitosan, a cationic biopolymer, in bentonite. Chitosan (CS)/bentonite nanocomposites were prepared by ionic exchange. The amino groups in the CS can be protonated in acidic solution and they can replace the interlayer cation on the clay surface. Nitrate (II) was added at the end of the preparation process for blocking the cationic exchange sites and enhance the potentiometric response to nitrate. Chitosan/bentonite films were obtained by solvent cast method. X-Ray Diffraction (XRD), X-Ray Photoelectron Spectroscopy (XPS) and Fourier-Transformed-Infrared Spectroscopy (FTIR) were used to characterize the nanocomposites. These studies confirm that the chitosan was intercalated into the bentonite interlayer spacing due to the electrostatic attraction between NH3+ groups and the negatively charge bentonite surface. These measurements confirm that there exist possibilities to reverse the ion exchange of this nanocomposite. Potentiometric measurements were performed using an Ag/AgCl reference electrode and an ISE with chitosan/bentonite membranes deposited on a graphite-epoxy electrode as a working electrode. A linear fitting was performed between 2×10-4M and 8×10-1M of concentration with a near Nernstian slope of -54.6 mV/dec. The selectivity towards some interfering ions was calculated according to the Separate Solution Method (SSM).
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