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Depth profiling X-ray photoelectron spectroscopy and atomic force microscopy of Cd(II)- and Pb(II)-selective electrodes based on nano metal sulfides

机译:基于纳米金属硫化物的CD(II) - 和Pb(II)和Pb(II)选择电极的深度分析X射线光电子能谱和原子力显微镜

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摘要

This research involved constructing and studying plastic membrane Cd(II)- and Pb(II)-ion selective electrodes of the coated wire type based on nanoparticles of CdS and PbS as ionophores, respectively. The electrodes exhibited average linear concentration ranges of 1.0 x 10(-6) to 1.0 x 10(-2) and 9.6 x 10(-7) to 1.0 x 10(-2) M, average detection limits of 8.6 x 10(-7) and 5.8 x 10(-7) M, pH ranges of 2.2-5.8 and 2.9-5.9, and average calibration graph slopes of 28.56 and 28.81 mV per concentration decade, respectively. Both electrodes showed high selectivity towards many inorganic cations. Depth profiling X-ray photoelectron spectroscopy of fresh and expired membranes proved that: (a) the nanoparticles were homogeneously dissolved in the polymeric network and (b) the limitation of the life span of the plastic membrane was due to leaching of the active ingredient from the membrane surface to the bathing solution. The topography of fresh, active, and expired membranes as imaged by atomic force microscopy revealed the formation of a gel layer at the surface of the active electrode and drastic deformation of the expired membrane's surface.
机译:该研究涉及基于CD和PBS的纳米颗粒和PBS作为离子团,构建和研究涂覆的线型的塑料膜CD(II)和Pb(II)选择性电极。电极显示出1.0×10(-6)至1.0×10(-2)和9.6×10(-7)至1.0×10(-2)m的平均线性浓度范围,平均检测限为8.6×10( - 7)和5.8×10(-7)m,pH范围为2.2-5.8和2.9-5.9,平均校准图分别为28.56和28.81mV的每浓度十年。两个电极对许多无机阳离子的选择性很高。新鲜和过期膜的深度分析X射线光电子能谱证明:(a)纳米颗粒均匀地溶解在聚合物网络中,(b)塑料膜的寿命的限制是由于活性成分的浸出膜表面到浴溶液。由原子力显微镜成像的新鲜,活性和过期膜的形貌揭示了在活性电极表面的凝胶层的形成,并且过期膜表面的剧烈变形。

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