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差分电位滴定法:通过一条滴定曲线确定金属(氢)氧化物零电荷点的方法的开发。

Differential potentiometric titration: development of a methodology for determining the point of zero charge of metal (hydr)oxides by one titration curve.

作者信息

Bourikas Kyriakos, Kordulis Christos, Lycourghiotis Alexis

机构信息

Department of Chemistry, University of Patras, GR-26500 Patras, Greece.

出版信息

Environ Sci Technol. 2005 Jun 1;39(11):4100-8. doi: 10.1021/es048139n.

Abstract

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.

摘要

本文提出了一种名为差分电位滴定法(DPT)的新方法,该方法仅通过一条电位滴定曲线就能测定金属(氢)氧化物的零电荷点(pzc)。通过对各种模型(氢)氧化物的电位滴定进行广泛模拟,我们发现,在H⁺(cons,surf)(消耗在(氢)氧化物表面的氢离子)与pH的电位滴定曲线中,拐点以及相应的差分曲线dH⁺(cons,surf)/dpH与pH中的峰值,出现在与模型(氢)氧化物假定的pzc相等的pH处。无论采用何种表面电离和界面模型以及假定的离子强度,这个可区分的峰值都出现在相同位置。研究发现,在实验测定的四种广泛应用于各种环境和其他技术领域的氧化物(SiO₂、TiO₂、γ -Al₂O₃和MgO)的高分辨率差分电位滴定曲线中,也出现了上述峰值。将DPT应用于上述氧化物得到的pzc值,与使用四种不同技术得到的相应值以及通过微电泳测定的相应等电点(iep)值实际相同。在MgO的情况下,使用各种技术测定的pzc和iep值之间的差异,归因于随着pH降低该氧化物溶解增加以及阳离子(Mg²⁺、Na⁺)在MgO/电解液界面上的吸附。

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