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Spectroscopic study of the dehydration and/or dehydroxylation of phyllosilicate and zeolite minerals

机译:页硅酸盐和沸石矿物的脱水和/或脱羟基的光谱研究

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摘要

Phyllosilicates on Mars mapped by infrared spectroscopic techniques could have been affected by dehydration and/or dehydroxylation associated with chemical weathering in hyperarid conditions, volcanism or shock heating associated with meteor impact. The effects of heat-induced dehydration and/or dehydroxylation on the infrared spectra of 14 phyllosilicates from four structural groups (kaolinite, smectite, sepiolite-palygorskite, and chlorite) and two natural zeolites are reported here. Pressed powders of size-separated phyllosilicate and natural zeolite samples were heated incrementally from 100°C to 900°C, cooled to room temperature, and measured using multiple spectroscopic techniques: midinfrared (400-4000 cm -1) attenuated total reflectance, midinfrared reflectance (400-1400 cm -1), and far-infrared reflectance (50-600 cm -1) spectroscopies. Correlated thermogravimetric analysis and X-ray diffraction data were also acquired in order to clarify the thermal transformation of each sample. For phyllosilicate samples, the OH stretching (∼3600 cm -1), OH bending (∼590-950 cm -1), and/or H 2O bending (∼1630 cm -1) bands all become very weak or completely disappear upon heating to temperatures > 500°C. The spectral changes associated with SiO 4 vibrations (∼1000 cm -1 and ∼500 cm -1) show large variations depending on the compositions and structures of phyllosilicates. The thermal behavior of phyllosilicate IR spectra is also affected by the type of octahedral cations. For example, spectral features of Al 3+-rich smectites are more stable than those of Fe 3+-rich smectites. The high-temperature (>800°C) spectral changes of trioctahedral Mg 2+-rich phyllosilicates such as hectorite, saponite, and sepiolite result primarily from crystallization of enstatite. Phyllosilicates with moderate Mg 2+ concentration (e.g., palygorskite, clinochlore) and dioctahedral montmorillonites (e.g., SAz-1 and SCa-3) with partial Mg 2+-for- Al 3+ substitution all have new spectral feature developed at ∼900 cm -1 upon heating to 800C. Compared with phyllosilicates, spectral features of two natural zeolites, clinoptilolite and mordenite, are less affected by thermal treatments. Even after heating to 900C, the IR spectral features attributed to Si (Al)-O stretching and bending vibration modes do not show significant differences from those of unheated zeolites. Copyright 2011 by the American Geophysical Union.
机译:通过红外光谱技术绘制的火星上的硅基硅酸盐可能已受到与高干旱条件下化学风化有关的脱水和/或脱羟基,与流星撞击有关的火山作用或冲击加热的影响。本文报道了热诱导的脱水和/或脱羟基作用对四种结构族(高岭石,蒙脱石,海泡石-坡缕石和绿泥石)和两种天然沸石中的14种页硅酸盐的红外光谱的影响。将大小分离的层状硅酸盐和天然沸石样品压制成粉的过程从100°C逐步加热到900°C,冷却至室温,并使用多种光谱技术进行测量:中红外(400-4000 cm -1)衰减的全反射率,中红外反射率(400-1400 cm -1)和远红外反射(50-600 cm -1)光谱仪。还获得了相关的热重分析和X射线衍射数据,以阐明每个样品的热转变。对于页硅酸盐样品,OH拉伸(〜3600 cm -1),OH弯曲(〜590-950 cm -1)和/或H 2O弯曲(〜1630 cm -1)带在加热时都变得非常弱或完全消失。温度> 500°C。与SiO 4振动(〜1000 cm -1和〜500 cm -1)相关的光谱变化显示出很大的变化,具体取决于页硅酸盐的组成和结构。页硅酸盐红外光谱的热行为也受到八面体阳离子类型的影响。例如,富含Al 3+的蒙脱石的光谱特征比富含Fe 3+的蒙脱石的光谱特征更稳定。富含三八面体Mg 2+的层状硅酸盐(如锂蒙脱石,皂石和海泡石)的高温(> 800°C)光谱变化主要是由于顽辉石的结晶所致。具有中等Mg 2+浓度的板硅酸盐(例如坡缕石,斜绿石)和部分被Mg 2+取代Al 3+取代的八面体蒙脱石(例如SAz-1和SCa-3)都具有在〜900 cm处形成的新光谱特征加热至800℃时为-1。与页硅酸盐相比,两种天然沸石(斜发沸石和丝光沸石)的光谱特征受热处理的影响较小。即使加热到900℃,归因于Si(Al)-O拉伸和弯曲振动模式的红外光谱特征与未加热的沸石相比也没有显示出显着差异。美国地球物理联盟版权所有2011。

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