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硫酸根离子对单分散α-Fe₂O₃颗粒形状和结构的控制机制

Mechanism of the Shape and Structure Control of Monodispersed alpha-Fe2O3 Particles by Sulfate Ions.

作者信息

Sugimoto T, Wang Y

机构信息

Institute for Advanced Materials Processing, Tohoku University, Katahira 2-1-1, Aobaku, Sendai, 980-8577, Japan

出版信息

J Colloid Interface Sci. 1998 Nov 1;207(1):137-149. doi: 10.1006/jcis.1998.5741.

Abstract

The characteristics of the adsorption of sulfate ions to hematite (alpha-Fe2O3) particles have been studied to elucidate the anisotropic growth of hematite particles in the presence of sulfate ions. Sulfate ions were actually found to be most strongly adsorbed to crystal faces parallel to the c-axis of the hexagonal crystal system from the adsorption isotherms of sulfate to hematite particles of different crystal habits, in accord with the retardation of their growth in the direction normal to the c-axis. It was found from FTIR spectroscopy that the adsorbed sulfate ions on the faces parallel to the c-axis, such as the {110} and {100} faces, or on {012} faces took the bidentate structure to Fe ions on the surfaces, while a monodentate structure was suggested for sulfate ions on the c-planes ({001} faces). The adsorbed amount of sulfate ions to the {012} faces of hematite at 100 degreesC decreased with increasing pH and became almost zero at pH >/=5, suggesting that the shape control with sulfate is possible only in the acidic media at pH < 5. EDX and chemical analysis revealed that sulfate ions were almost uniformly incorporated into the ellipsoidal or peanut-type particles during their growth in the presence of sulfate ions. On the other hand, sulfate ions in the solution phase with a high concentration of chloride ions such as 3.0 mol dm-3 were likely to be present in the form of free ions without forming a complex with Fe3+, as suggested from UV spectroscopy at 25 degreesC. When the concentration of sulfate ions in the solution phase exceeded the level for shape control of hematite, precipitation of acicular alpha-FeOOH (goethite) was observed. If hematite particles were present in such a system, alpha-FeOOH was grown as whiskers on the hematite particles. When [SO2-4] in the solution phase was higher than 0.1 mol dm-3, precipitation of basic ferric sulfate was also observed in addition to the growth of alpha-FeOOH whiskers on hematite. Copyright 1998 Academic Press.

摘要

为了阐明在硫酸根离子存在下赤铁矿颗粒的各向异性生长,对硫酸根离子在赤铁矿(α-Fe₂O₃)颗粒上的吸附特性进行了研究。从不同晶习的赤铁矿颗粒对硫酸根的吸附等温线可以看出,硫酸根离子实际上最强烈地吸附在平行于六方晶系c轴的晶面上,这与它们在垂直于c轴方向上生长的迟缓现象相一致。通过傅里叶变换红外光谱(FTIR)发现,吸附在平行于c轴的晶面(如{110}和{100}面)或{012}面上的硫酸根离子与表面的铁离子形成双齿结构,而对于c面({001}面)上的硫酸根离子则推测为单齿结构。在100℃时,硫酸根离子在赤铁矿{012}面上的吸附量随pH值升高而降低,在pH≥5时几乎为零,这表明只有在pH<5的酸性介质中才能通过硫酸根进行形状控制。能量散射X射线光谱(EDX)和化学分析表明,在硫酸根离子存在下颗粒生长过程中,硫酸根离子几乎均匀地掺入椭圆形或花生形颗粒中。另一方面,从25℃下的紫外光谱推测,在高浓度氯离子(如3.0 mol dm⁻³)的溶液相中,硫酸根离子可能以游离离子形式存在,而不与Fe³⁺形成络合物。当溶液相中硫酸根离子的浓度超过赤铁矿形状控制的水平时,会观察到针状α-FeOOH(针铁矿)的沉淀。如果在这样的体系中存在赤铁矿颗粒,α-FeOOH会在赤铁矿颗粒上以晶须形式生长。当溶液相中[SO₄²⁻]高于0.1 mol dm⁻³时,除了在赤铁矿上生长α-FeOOH晶须外,还会观察到碱式硫酸铁的沉淀。版权所有1998年,学术出版社。

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