蛇纹石族矿物及其热转变产物的红外光谱研究

本文报道了蛇纹石族矿物及其热转变产物的红外光谱。在室温下斜纤蛇纹石,正纤蛇纹石,叶蛇纹石和利蛇纹石都具有各自的特征光谱。在结构资料基础上,我们解释了它们之间的光谱差异。无疑,红外光谱是区分各种蛇纹石矿物的有效手段。 样品加热到600—700℃时,3680cm~(-1)羟基带消失,这表明在该温度下蛇纹石矿物完全脱羟。与此同时,光谱中出现橄榄石870cm~(-1)的最强带和一个宽带1000cm~(-1),这说明蛇纹石已部分地转变为晶质橄榄石和形成一个无定形的中间相。800℃时,1060cm~(-1)新带的出现标志着顽火辉石的生成。在所有加热样品的光谱中都没有发现SiO_2吸收带,故可认为,在蛇纹石的热转变过程中没有出现SiO_2相。     

合成斜方辉石系列的红外光谱研究

在30kbar和900℃条件下,用等化学计量氧化物混合物合成了11个斜方辉石系列的样品,并对合成的样品进行了X射线粉晶分析和红外光谱分析。分析结果表明,晶胞参数和红外光谱随化学成分的改变而产生复杂的变化。不仅晶胞参数b和M而且频率ν_(670cm)-1和M之间存在很好的线性相关关系,通过用最小二乘法所拟合的相关方程可容易地测定斜方辉石的成分,但是α和c与M之间只有较差的线性关系,而ν_(450cm)-1和M以及ν_(380cm)-1和M之间并无简单的线性相关关系,这可归因于Fe~(2+)在M_1和M_2位置的有序分布。     

新疆库布苏金矿石英标型特征研究

重点研究了库布苏矿化带中石英脉与金矿化关系，对不同成矿阶段石英的化学成分，晶胞参，红外光谱，热发光，包裹体等进行了研究，总结了找矿矿物学标志。     

内蒙赤峰莲花山金矿田石英脉的红外光谱成矿信息及定量预测

测试了１３０余件含金石英脉及不含金石英脉的红外光谱试样，查明了该区含金石英脉的红外光谱特征，同时配合其它预测含金石英脉的测量方法，提出了该区含金石英脉的预测靶区，经过初步验证，预测基本上是准确的。     

Vertical column abundances of HCN deduced from ground-based infrared solar spectra: Long-term trend and variability

A set of high-resolution IR solar spectra recorded at the International Scientific Station of the Jungfraujoch, Switzerland, from 84/06 to 93/06, and at the National Solar Observatory McMath-Pierce solar telescope facility on Kitt Peak, Arizona, U.S.A. from 78/05 to 92/07 have been analyzed to determine the vertical column abundances of hydrogen cyanide, HCN, above the two stations. The analysis was based on least-squares curve fitting of calculated spectra to the observations encompassing the P4 and the P8 lines of HCN respectively located at 3299.5273 and 3287.2483 cm^–1. The results obtained for the two stations indicate that no significant long-term trend affects either of the two databases; however, this analysis reveals variable increases during springtime of up to a factor of 2 in the HCN total column above the Jungfraujoch and even up to 3 above Kitt Peak. The calculated mean vertical column abundances, excluding the spring observations, are equal to (2.55±0.30)×10¹⁵ molec./cm² (S.D.) and (2.75±0.30)×10¹⁵ molec./cm² respectively above the Jungfraujoch and the Kitt Peak observatories. Based on a realistic volume mixing ratio profile, these columns translate into mean volume mixing ratios equal to 190×10^–12 ppv at the respective altitudes of the stations.     

Application of short-wave infrared spectroscopy to define alteration zones associated with the Elura zinc–lead–silver deposit, NSW, Australia

Short-wave infrared reflectance spectra obtained from a Portable Infrared Mineral Analyser (PIMA) have been used to define alteration zones adjacent to base metal sulfide ore bodies at the Elura Mine, Cobar, Australia. The spectroscopic work identified white mica (sericite), chlorite and carbonates of hydrothermal origin in the alteration zones associated with the ore bodies. Weathering, alteration and ore zones can be discriminated by variations in the intensity and wavelength of relevant absorption features. Hydrothermal alteration is classified into four principal types, namely sericitic, silicic, chloritic and carbonate alteration. The first three types comprise overprinting hydrothermal assemblages of quartz, sericite, chlorite, ankerite, siderite, calcite and sulfides developed in strongly altered metasiltstone and slate of Early Devonian age, adjacent to the zinc–lead–silver mineralisation. An extensive zone of carbonate alteration, manifested as porphyroblasts of siderite in the host metasediments, is recognised beyond the zones of strong alteration. Spectral analysis is consistent with the mineralogical data obtained from XRD and XRF analyses and defines the limits of the alteration zones to distances of about 80 m around the ore bodies. The study demonstrates the potential for spectral analysis to assist with drill hole logging and the identification of alteration zones as part of mineral exploration and development programs.     

南极中山站以南地区冰面高程信息的提取

在实地高程控制点与热红外影像上同名像点的辐射亮度值间建立函数关系，从Ｌａｎｄｓａｔ４ＴＭ６影像上提取出中山站附近冰面的高程信息，并绘制成冰面地形图。     

Measurements of stratospheric chlorine monoxide (ClO) from groudbased FTIR observations

Infrared absorption features due to ClO in the lower stratosphere have been identified from groundbased solar absorption spectra taken from Aberdeen, U.K. (57° N, 2° W) on 20 January 1995. A vertical column abundance of 3.42 (±0.47)×10¹⁵ molec cm^-2 has been derived from 13 independent absorption features in the P and R branches of the (0–1) vibration-rotation band of ³⁵ClO, spanning the spectral region 817–855 cm^-1. The observed absorption features are consistent with very high levels of ClO (approximately 2.6 parts per billion by volume (ppbv)) in the altitude range 16–22 km. A comparison of this profile with a 3D chemical transport model profile indicates the observation was made inside the polar vortex and shows good qualitative agreement but the model underestimates the concentrations of ClO. Simultaneous measurements of other species were made including HCl, HF and ClONO₂. These columns yield a value for HCl+ClONO₂+ClO of 7.02±0.65×10¹⁵ molec cm^-2. This is lower than the total inorganic chlorine (ClO _y ) column of 10.7±1.6×10¹⁵ molec cm^-2 estimated from mean measured (HCl+ClONO₂)/HF ratios together with in-vortex HF measurements. The discrepancy is probably due to significant amounts of the ClO dimer (Cl₂O₂) in the lower part of the stratosphere. The measurements of highly elevated levels of ClO are used to estimate O₃ loss rates at the 400, 475 and 550 K levels making assumptions about the probable distribution of ClO and Cl₂O₂. These are compared with loss rates derived from ozone sonde data.     

偏岭石及煅烧高岭石的红外光谱研究

通过对偏岭石和相应煅烧高岭石的红外光谱测定,发现偏岭石同煅烧高岭石在结构上有很大的差异。在偏岭石中不存在非晶态SiO_2相,其中Si—O_4四面体同Al—O_6八面体是相互聚合的:煅烧高岭石(600～995℃)中则不同,其中Si大部分是以独立的非晶态SiO_2相存在,而同其中的Al_2O_3相分离。偏岭石同煅烧高岭石的关系是:对偏岭石进行一定温度的煅烧,它可以转变成像煅烧高岭石一样的结构状态。     

石膏热学性质的实验研究

用差示扫描１热仪测定石膏（ＣａＳＯ＿４·２Ｈ２Ｏ）的脱水活化能；用红外光谱仪研究掺入微量Ｅｕ￣（３＋），Ｍｎ￣（２＋），Ｐｂ￣（２＋）后，在不同温度煅烧下产物的红外光谱图，并测定其热发光性质；对石膏以及掺杂后的热学性质进行了讨论。