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硒酸盐和硫酸盐在铁和铝(氢)氧化物表面吸附机制的振动光谱研究

Vibrational Spectroscopy Study of Selenate and Sulfate Adsorption Mechanisms on Fe and Al (Hydr)oxide Surfaces.

作者信息

Wijnja H, Schulthess CP

机构信息

The Connecticut Agricultural Experiment Station, New Haven, Connecticut, 06504

出版信息

J Colloid Interface Sci. 2000 Sep 1;229(1):286-297. doi: 10.1006/jcis.2000.6960.

Abstract

The coordination and speciation of selenate (SeO(4)) and sulfate (SO(4)) on goethite and Al oxide were studied using Raman and ATR-FTIR spectroscopy. Raman spectra were collected from pastes of suspensions containing 4 mM SeO(4) or SO(4). For SO(4), complementary data were collected by ATR-FTIR spectroscopy in goethite systems with 1 mM SO(4) and in Al oxide systems with 4 mM SO(4). The combined data set of Raman and ATR-FTIR spectra indicate that both inner- and outer-sphere surface complexes of SeO(4) and SO(4) occur on these metal (hydr)oxide surfaces. These spectral data show that SeO(4) and SO(4) have a similar complexation behavior on the same adsorbent. On goethite, these form predominantly monodentate inner-sphere surface complexes at pH <6, while at pH >6 these anions exist predominantly as outer-sphere surface complexes. On Al oxide, in contrast, these anions exist predominantly as outer-sphere surface complexes, but a small fraction is also present as an inner-sphere complex at pH <6. A comparison of the spectral intensities of these anions on goethite and Al oxide shows that complexation of these anions with Al oxide is weaker than with Fe oxide. Copyright 2000 Academic Press.

摘要

利用拉曼光谱和衰减全反射傅里叶变换红外光谱(ATR-FTIR)研究了硒酸盐(SeO(4))和硫酸盐(SO(4))在针铁矿和氧化铝上的配位作用及形态。从含有4 mM SeO(4)或SO(4)的悬浮液糊剂中收集拉曼光谱。对于SO(4),通过ATR-FTIR光谱在含有1 mM SO(4)的针铁矿体系和含有4 mM SO(4)的氧化铝体系中收集补充数据。拉曼光谱和ATR-FTIR光谱的综合数据集表明,SeO(4)和SO(4)的内球和外球表面配合物均存在于这些金属(氢)氧化物表面。这些光谱数据表明,SeO(4)和SO(4)在同一吸附剂上具有相似的络合行为。在针铁矿上,在pH <6时,它们主要形成单齿内球表面配合物,而在pH >6时,这些阴离子主要以外球表面配合物形式存在。相比之下,在氧化铝上,这些阴离子主要以外球表面配合物形式存在,但在pH <6时,也有一小部分以内球配合物形式存在。这些阴离子在针铁矿和氧化铝上的光谱强度比较表明,这些阴离子与氧化铝的络合作用比与氧化铁的络合作用弱。版权所有2000年学术出版社。

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