新疆喀喇昆仑大红柳滩一带锂矿光谱特征及其找矿指示意义

近年来,新疆喀喇昆仑大红柳滩地区锂铍矿取得重大找矿发现,显示良好的成矿潜力。受其高寒深切割环境的制约,矿区外围的地质找矿工作推进不易。前人利用高分、多光谱遥感数据及高光谱技术在该区花岗伟晶岩型锂铍矿找矿工作中发挥出积极作用,发现了505、507、俘虏沟南1号、俘虏沟南2号等多处大型锂铍矿产地。笔者通过对区内花岗伟晶岩型锂矿床中岩、矿石开展地面光谱测试,系统对比不同岩性赋矿地层、岩体、含矿伟晶岩、不含矿伟晶岩的光谱特征。通过光谱解算剖析其矿物组合,分析显示含矿伟晶岩中含锂矿物以锂辉石、锂云母为主,少量锂绿泥石。含矿伟晶岩具高反射率,发育强Al-OH吸收峰,受其接触交代蚀变影响,发育Mg-OH吸收峰,二者共同构成区内含矿伟晶岩的标志性遥感异常组合。采用国产高光谱遥感卫星数据,利用匹配滤波方法提取上述异常组合,圈定找矿有利区7处,为该区下一步锂铍找矿工作提供了依据。

Structural and Infrared Spectroscopic Study on Solvation of Acetylene by Protonated Water Molecules

The effect of solvation on the conformation of acetylene has been studied by adding one water molecule at a time. Quantum chemical calculations of the n＋ （C2H2）（H2O）n （n=1-5） clusters indicate that the H2O molecules prefer to form the OH...Tr interaction rather than the CH...O interaction. This solvation motif is different from that of neutral （C2H2）（H2O）n （n=1-4） clusters, in which the H2O molecules prefer to form the CH...O and OH...C Hbonds. For the H＋（C2H2）（H2O）n cationic clusters, the first solvation shell consists of one ring structure with two OH...Tr H-bonds and three water molecules, which is completed at n=4. Simulated infrared spectra reveal that vibrational frequencies of OH... H-bonded O-H stretching afford a sensitive probe for exploring the solvation of acetylene by protonated water molecules. Infrared spectra of the H＋ （C2H2）（H2O）n （n=1-5） clusters could be readily measured by the infrared photodissociation technique and thus provide useful information for the understanding of solvation processes.

Infrared Photodisssociation Spectroscopy of Boron Carbonyl Cation Complexes

The boron carbonyl cation complexes B（CO）3＋, B（CO）4＋ and B2（CO）4＋ are studied by infrared photodissociation spectroscopy and theoretical calculations. The B（CO）4＋ ions are characterized to be very weakly bound complexes involving a B（CO）3＋ core ion, which is predicted to have a planar D3h structure with the central boron retaining the most favorable 8-electron configuration. The B2（C0）4＋ cation is determined to have a planar D2h structure involving a B-B one and half bond. The analysis of the B-CO interactions with the EDA- NOCV method indicates that the OC→B cr donation is stronger than the B-＋CO π back donation in both ions.

An Approach to Underwater Image Enhancement Based on Image Structural Decomposition

Underwater imaging posts a challenge due to the degradation by the absorption and scattering occurred during light propagation as well as poor lighting conditions in water medium Although image filtering techniques are utilized to improve image quality effectively, problems of the distortion of image details and the bias of color correction still exist in output images due to the complexity of image texture distribution. This paper proposes a new underwater image enhancement method based on image struc- tural decomposition. By introducing a curvature factor into the Mumford_Shah_G decomposition algorithm, image details and struc- ture components are better preserved without the gradient effect. Thus, histogram equalization and Retinex algorithms are applied in the decomposed structure component for global image enhancement and non-uniform brightness correction for gray level and the color images, then the optical absorption spectrum in water medium is incorporate to improve the color correction. Finally, the en- hauced structure and preserved detail component are re.composed to generate the output. Experiments with real underwater images verify the image improvement by the proposed method in image contrast, brightness and color fidelity.

Infrared Photodissociation Spectroscopic and Theoretical Study of [Co（CO2）n]+ Clusters

The mass-selected infrared photodissociation (IRPD) spectroscopy was utilized to investigate the interactions of cationic cobalt with carbon dioxide molecules. Quantum chemical calculations were performed on the [Co(CO2)n]^+ clusters to identify the structures of the low-lying isomers and to assign the observed spectral features. All the [Co(CO2)n]^+(n=2-6) clusters studied here show resonances near the CO2 asymmetric stretch of free CO2 molecule. Experimental and calculated results indicate that the CO2 molecules are weakly bound to the Co+ cations in an end-on con guration via a charge-quadrupole electrostatic interaction. The present IRPD spectra of [Co(CO2)n]^+ clusters have been compared to those of Ar-tagged species ([Co(CO2)n]^+-Ar), which would provide insights into the tagging effect of rare gas on the weakly-bounded clusters.

Infrared Spectroscopy of CO2 Transformation by Group Ⅲ Metal Monoxide Cations

Infrared photodissociation spectroscopy of mass-selected[MO(CO2)n]^+(M=Sc,Y,La)complexes indicates that the conversion from the solvated structure into carbonate one can be achieved by the ScO^+ cation at n=5 and by the YO^+ cation at n=4,while only the solvated structures are observed for the LaO^+ cation.These findings suggest that both the ScO^+ and YO^+cations are able to fix CO2 into carbonate.Quantum chemical calculations are performed on[MO(CO2)n]^+ to identify the structures of the low-lying isomers and to assign the observed spectral features.Theoretical analyses show that the[YO(CO2)n]^+ complex has the smallest barrier for the conversion from the solvated structure into carbonate one,while[LaO(CO2)n]^+ exhibits the largest conversion barrier among the three metal oxide cations.The present system affords a model in clarifying the effect of different metals in catalytic CO2 transformation at the molecular level.