1-PK MULTISITES DESCRIPTION OF CHARGE DEVELOPMENT AT THE AQUEOUS ALUMINA INTERFACE - ADSORPTION OF PD-II-AMINE COMPLEXES

被引:27
作者
CONTESCU, C
HU, JF
SCHWARZ, JA
机构
[1] SYRACUSE UNIV, DEPT CHEM ENGN & MAT SCI, SYRACUSE, NY 13244 USA
[2] ROMANIAN ACAD, INST PHYS CHEM, R-77208 BUCHAREST, ROMANIA
[3] FUDAN UNIV, SHANGHAI, PEOPLES R CHINA
来源
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS | 1993年 / 89卷 / 22期
关键词
D O I
10.1039/ft9938904091
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Potentiometric titration data for gamma-Al2O3 have been converted to proton-binding curves and deconvoluted, which gave the pH-dependent number and strength of surface groups with different proton acceptor/donor properties. The deconvoluted isotherm was reconstructed based on the assumption of a 1-pK multisites description of the amphoteric gamma-Al2O3 surface. We find that our picture of the oxide surface as consisting of structurally non-equivalent oxo and hydroxo groups allows for assignment of proton-binding processes to hydroxy groups with different acidic/basic properties, as determined independently from infrared spectra. Furthermore, we find that, based on models of the gamma-Al2O3 surface consisting of individual low-index planes, the development of surface charge as a function of pH has completely different characteristics on different surface planes. Adsorption of [Pd(NH3)(4)](2+) cations was measured at fixed ionic strength and varying pH and initial concentration. Although the pH dependence of adsorbed amounts could be predicted on the basis of the 1-pK multisites description, the effects of concentration could not be described exactly. In conjunction with results from temperature-programmed reduction and UV-VIS spectroscopy, we propose the concept of geometrical constraints during adsorption-impregnation of precursor ions on the manifold of charged sites revealed by proton-transfer reactions.
引用
收藏
页码:4091 / 4099
页数:9
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