Ajadi Abdulhakeem A, Shuaib Nadia M, Shoukry Adel F
Chemistry Department, Faculty of Science, Kuwait University Kuwait
RSC Adv. 2018 Jan 17;8(7):3574-3581. doi: 10.1039/c7ra13168b. eCollection 2018 Jan 16.
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 × 10 to 1.0 × 10 and 9.6 × 10 to 1.0 × 10 M, average detection limits of 8.6 × 10 and 5.8 × 10 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.
本研究分别基于硫化镉和硫化铅纳米颗粒作为离子载体,构建并研究了涂层丝型塑料膜镉(Ⅱ)和铅(Ⅱ)离子选择性电极。这些电极的平均线性浓度范围分别为1.0×10至1.0×10以及9.6×10至1.0×10 M,平均检测限分别为8.6×10和5.8×10 M,pH范围分别为2.2 - 5.8和2.9 - 5.9,平均校准曲线斜率分别为每浓度 decade 28.56和28.81 mV。两种电极对许多无机阳离子都表现出高选择性。对新鲜和过期膜的深度剖析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)塑料膜寿命的限制是由于活性成分从膜表面浸出到浴液中。通过原子力显微镜成像的新鲜、活性和过期膜的形貌揭示了活性电极表面形成了凝胶层以及过期膜表面的剧烈变形。