A new methodology is presented, called differential potentiometric titration (DPT), which allows the determination of the point of zero charge (pzc) of metal (hydr)oxides using only one potentiometric curve. By performing extensive simulations of potentiometric titrations for various model (hydr)oxides, we found that an inflection point in a H+(cons,surf) versus pH potentiometric curve (H+(cons,surf): hydrogen ions consumed on the surface of the (hydr)oxide) and a peak in the corresponding differential curve, dH+(cons,surf)/dpH versus pH, appear at a pH equal to the pzc assumed for a model (hydr)oxide. This distinguishable peak appears at the same position irrespective of the surface ionization and the interfacial model adopted as well as the assumed ionic strength. It was found that the aforementioned peak also appears in the high-resolution differential potentiometric curves experimentally determined for four oxides (SiO2, TiO2, gamma-Al2O3, and MgO) that are widely used in various environmental and other technological applications. The application of DPT to the above-mentioned oxides provided practically the same pzc values as the corresponding ones achieved by using four different techniques as well as the corresponding isoelectric point (iep) values determined by microelectrophoresis. Differences between the pzc and iep values determined using various techniques in the case of MgO were attributed to the increasing dissolution of this oxide as pH decreases and the adsorption of cations (Mg2+, Na+) on the MgO/electrolytic solution interface.
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http://dx.doi.org/10.1021/es048139n | DOI Listing |
Anal Chem
November 2024
Department of Inorganic and Analytical Chemistry, University of Geneva, Quai Ernest-Ansermet 30, CH-1211 Geneva, Switzerland.
Self-powered potentiometric sensors spontaneously respond to activity changes of target species without the need for an external power source. Here, a self-powered potentiometric sensing approach is described that may store concentration perturbations that occur before the sensor readout through a combination of capacitors and diodes. Two channels, termed "more than" and "less than" operators, are utilized as memory modules in the sensor circuit to record positive and negative concentration excursions, respectively.
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October 2023
Analytical Chemistry Department, Faculty of Pharmacy, Cairo University, Egypt. Electronic address:
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Institute of Crystallography, CNR, P. Gaifami 18, Catania 95126, Italy.
Analyst
February 2024
Institute of Chemistry, University of Tartu (UT), Ravila Street 14a, 50411 Tartu, Estonia.
Mobile phase pH is a critically important parameter in reversed-phase liquid chromatographic (RPLC) separations involving analytes that display acidic or basic properties in the pH range used for the mobile phase. The main problem in measuring mobile phase pH lies in the fact that RPLC mobile phases are typically aqueous-organic mixtures. In addition to experimental difficulties, the pH values refer to different aqueous-organic compositions that cannot be correctly compared.
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January 2024
Department of Chemistry, J.J. Strossmayer University of Osijek, Cara Hadrijana 8/A, 31000 Osijek, Croatia.
Gallic acid and its metal complexes are good antioxidants that could be used to increase the body's immune system against degenerative and viral diseases. Therefore, such complexes could be used as a good alternative to supplementary medicines and may have potential significance in clinical trials. Differential pulse voltammetry, UV/VIS spectroscopy, and potentiometry were used to analyse the complexation of gallic acid with calcium in this study.
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