Glasauer S, Friedl J, Schwertmann U
College of Biological Science, University of Guelph, Guelph, Ontario, N1G 2W1, Canada
J Colloid Interface Sci. 1999 Aug 1;216(1):106-115. doi: 10.1006/jcis.1999.6285.
Goethite in natural environments usually grows in the presence of dissolved silicate. To study silicate-associated goethite with specific properties, goethite was synthesized in an Fe(III) system at RT under acidic (OH/Fe = 2; pH 1.6-1.8) and basic (OH/Fe = 4; pH 12-13) conditions at Si concentrations between 10(-5) and 1 M. The goethites were characterized by transmission (TEM) and scanning (SEM) microscopy, X-ray diffraction (XRD), Mössbauer spectroscopy (MS), and chemical analyses. Despite large differences in size and morphology, all goethite crystals were dominantly bound by 110 and 021 faces. Nanosized crystals (ca. 20 nm) were formed at low pH, where the influence of Si was weak. In the basic system, where Si retarded crystallization, much larger (tens to hundreds of nanometers) crystals were formed whose shape varied from acicular and multidomainic at low Si (10(-5) M) to monodomainic, blocky crystals at high (10(-2) M) Si concentration that had reduced growth along [001] in favor of [100] and [010]. The sizes and shapes of the crystals are discussed in terms of nuclei and growth unit concentrations in the system. Part of the retained Si could be released by phosphate and NaOH (surface-Si), and part was only liberated into HCl congruently with Fe (up to 46 and 17 g kg-1 for the acid and basic goethites, respectively). Neither XRD nor MS were able to prove structural Si-for-Fe substitution, probably because no tetrahedral positions are available to accommodate Si in the goethite structure. It is assumed that this nonsurface Si fraction is located between the crystal domains. Copyright 1999 Academic Press.
在自然环境中,针铁矿通常在溶解硅酸盐存在的情况下生长。为了研究具有特定性质的与硅酸盐相关的针铁矿,在室温下于铁(III)体系中,在酸性(OH/Fe = 2;pH 1.6 - 1.8)和碱性(OH/Fe = 4;pH 12 - 13)条件下,以10⁻⁵至1 M的硅浓度合成了针铁矿。通过透射电子显微镜(TEM)、扫描电子显微镜(SEM)、X射线衍射(XRD)、穆斯堡尔光谱(MS)和化学分析对针铁矿进行了表征。尽管尺寸和形态存在很大差异,但所有针铁矿晶体主要由110面和021面结合。在低pH值下形成了纳米级晶体(约20纳米),此时硅的影响较弱。在碱性体系中,硅延缓了结晶过程,形成了大得多(几十到几百纳米)的晶体,其形状从低硅(10⁻⁵ M)时的针状和多畴状变化为高硅(10⁻² M)浓度时的单畴块状晶体,[001]方向的生长受到抑制,有利于[100]和[010]方向。根据体系中的晶核和生长单元浓度对晶体的尺寸和形状进行了讨论。部分保留的硅可被磷酸盐和氢氧化钠释放(表面硅),部分仅与铁一起被盐酸完全释放(酸性和碱性针铁矿分别高达46和17 g kg⁻¹)。XRD和MS都无法证明结构上硅取代了铁,可能是因为在针铁矿结构中没有四面体位置来容纳硅。据推测,这部分非表面硅位于晶畴之间。版权所有1999年学术出版社。