Surface chemical analysis in coal preparation research: complementary information from XPS and ToF-SIMS

The application of X-ray photoelectron spectroscopy (XPS) to coal surface characterisation for preparation research is described. Progress towards the acquisition of complementary surface chemical information by time-of-flight secondary ion mass spectrometry (ToF-SIMS) is also discussed. Surface-based beneficiation techniques such as flotation are assuming greater importance as the proportion of fines in raw coal increases due to the proliferation of high capacity mining methods. A necessary condition for the floatability of a coal particle is adequate hydrophobicity, and the degree of hydrophobicity of the flotation concentrate is one factor influencing the ease with which its dewatering can be affected. The hydrophobicity of a coal is very difficult to measure directly because of microporosity, and it is often necessary to deduce the degree of hydrophobicity from a knowledge of the surface chemistry. XPS is able to provide sufficient analytical data to allow relative levels of hydrophobicity to be estimated. In principle, ToF-SIMS should be able to supply additional information enabling refinement of such estimates; however, there are insufficient data at present to allow the ionic fragments detected to be related to specific functional groups at the coal surface.     

碳酸盐岩的反射光谱特征的研究及应用

在室内对新疆塔里木盆地西北缘柯坪地区碳酸盐岩的反射光谱进行了测量。分析结果表明：碳酸盐岩的特征吸收谱带位于２３００～２３５０ｎｍ，随着碳酸盐岩中Ｍｇ２＋含量的增加，其特征吸收谱带的中心波长位置具有向短波长方向移动的特点；同时，随着碳酸盐岩中碳酸盐矿物含量的增加，其特征吸收谱带的深度（Ｄ）也有增大的趋势，并且岩石的平均反射率（Ｒ）也随着增高。根据这些特征可以判定碳酸盐岩的岩石类型及碳酸盐矿物的相对含量     

VICARIOUS RADIOMETRIC CALIBRATION OF SATELLITE FY-ID SENSORS AT VISIBLE AND NEAR INFRARED CHANNELS

For the problem of in-flight test site radiometric calibration for the FY-1D Meteorological Satellite onboard sensor's visible and near infrared channels,this paper described the calibration method,satellite-ground synchronous observation data acquired at China Dunhuang Calibration Test Site,parameter derivation and radiative transfer computation during the calibration,and the calibration result analysis.At FY-1D seven channels (with central wavelength at Channels 1:630 nm,2:865 nm;6:1610 nm;7:455 nm,8:505 nm;9:555 nm;10:932 nm),calibration coefficients obtained during the ground site calibration were compared with that respectively of prelaunch calibration.It is demonstrated that results of FY-1D onboard two sensors' (A and B) at channels 1,2,6 and 10 were close to pre-calibration,and the absolute difference of Gobi desert reflectance computed using test site and pre-launch calibration coefficients was no more than 2%. At other channels,large pre-launch calibration errors resulted in a poor consistency between the test site and pre-launch calibration.The errors can be corrected by the test site calibration results. Based on a rough estimation,the overall error of the calibration was about 6%. The paper also presented the in-flight vicarious calibration at the visible and near infrared channels of FY-1C sensor A which was launched in 1999 and has been put into operational mode since 2002.The results exhibit that FY-1C sensor's response has 23% attenuation at Channels 7 and 8,while only minor degradation at the other channels was found. During the mission,calibrations were also conducted at NOAA-17's Channels 1 and 2 (1:430-830 nm,2:500-1072 nm).A very good consistency has been achieved between the test site and pre-launched calibration results.     

A comparative study on the illite crystallinity and the clay mineral reflectance spectral index for subdividing the very low-grade metamorphic belt along the Lizhou-Hekou geological section in the Youjiang sedimentary basin, Guangxi, China

To examine the application potential of hyperspectral remote sensing techniques in classifying very low-grade metamorphic belts, the composition of clay minerals and the cyrstallinity of illite from mudstones were measured using XRD and VIS-SWIR (400-2500 nm) reflectance spectroscopy. Based on the illite cyrstallinity, Kubler Index (KI), the Early Triassic LuoLou Group and the Middle Triassic lower Baifeng Formation were classified as the lower Epizone with KI△2θ° ranging from 0.22 to 0.25, the upper Baifeng Formation as upper anchizone with KI△2θ°ranging from 0.26 to 0.33, and the Hekou Formation as lower anchizone with KI△2θ° ranging from 0.38 to 0.40. According to a KI△2θ° value of 0.43, it is possible that there may exist a local diagenetic zone in the upper strata. The illite cyrstallinity Kubler index and the metamorphic grade increase from the bottom to the top of the stratigraphic sequence. The metamorphic grade boundaries nearly match the stratigraphic boundaries, indicating a burial metamorphism nature for the stratigraphic sequence. From the bottom to the top of the sequence, the spectral absorption band center of clay minerals from fresh rocks is around 2200 nm. The absorption band centers change towards shorter wavelengths: the Luolou Group being at 2220 nm, the Baifeng Formation at 2217-2213 nm, the lower member of the Hekou Formation at 2214-2206 nm, and the upper member of the Hekou Formation at 2205-2197 nm. The spectral absorption band center of illite shows the same change pattern. These results indicate that very low-grade metamorphic belts can be subdivided using spectral indices of clay minerals, which are measured by using field portable spectroradiometers. However, it may not work well with satellite and airborne sensors.     

Thermal decomposition of NH4-analcime

The thermal decomposition of ammonium-exchanged natural analcime is characterized by gas chromatography, IR spectroscopy and X-ray diffraction. The de-ammoniation and dehydroxylation proceed in parallel throughout the decomposition, which evidences the instability of the protonated analcime framework. The mechanism of degassing of NH₄-analcime changes throughout its decomposition. At the initial step, the mechanism of de-ammoniation consists in thermal dissociation of NH₄⁺ molecule onto NH₃ and proton (framework OH group) and diffusion of NH₃ out of the structure. Subsequent decomposition and removal of the OH groups lead to a progressive loss of crystallinity. At this step, an apparent activation energy for NH₃ desorption is estimated to be 145(±13) kJ mol^–1. This value is within the upper limit of the activation energy characteristic for the NH₃ desorption from proton centres in large-pore zeolites. At the final step, the adsorption of NH₃ and protons onto the defect centres in the amorphosed aluminosilicate framework results in a significant increase of an apparent activation energy for the de-ammoniation and dehydroxylation up to 270(±20) kJ mol^–1.     

Sorption Characteristics of Rare Earth Element Eu^3＋ onto Silica-Water Interfaces Studied by Fluorescence Spectroscopy

The sorption of Eu species onto nano-size silica-water interfaces was investigated using fluorescence spectroscopy for Ph ranges of 1-8.5 and an initial Eu concentration (Ceu) of 2×10-4 M. The sorption rate of Eu was initially low, but significantly increased at Ph>4. The sorption density of Eu species on a silica surface was ～1.58×10-7 mol/m2 when the dissolved Eu species were completely sorbed onto silica-water interfaces at Ph=～5.8. The sorbed Eu species at Ph<6 is aquo Eu3 , which is sorbed onto silica-water interfaces as an outer-sphere complex at Ph<5, but may be sorbed as an inner-sphere bidentate complex at 5相似文献   

一种改进的MODIS影像BRDF辐射校正方法

针时二向性造成的辐射失真，在核驱动模型的基础上提出了一种改进的二向性反射分布模型，并通过时MODIS影像的试验，得到了减弱辐射差异的较好效果，并对试验结果进行了分析和评价。     

应用高光谱遥感数据估算土壤表层水分的研究

土壤水分是土壤的重要组成部分，它在陆地表层和大气之间的物质和能量交换方面扮演着重要角色，寻求快速而准确的方法估算土壤水分具有重要意义。通常，从可见光一近红外对土壤表层水分的估计多是建立在土壤水分与反射率的关系之上的。而在土壤水分含量不高时，土壤水分的增加使土壤光谱反射率在整个波长范围内降低，尤其在760nm，970nm，1190nm，1450nm，1940nm和2950nm等水分吸收波段，而在土壤水分含量较高时，土壤水分的增加会使土壤光谱反射率在某些光谱波段升高。而土壤水分的估计往往是基于土壤水分与土壤水分吸收波段的吸收强度之间的线性关系上，虽然这些经验的方法对于估算某些土壤的表层水分含量是有效的，但这些关系应用于其它条件(如不同种类土壤、土壤湿度变化范围很大的情况)时却面临很多困难，这与土壤的光谱反射率是由土壤的组成成分(土壤水分、有机质、氧化铁和粘土矿物等)的含量和它们在土壤中的分布密切相关。微分技术处理“连续”的光谱是遥感中常用的数学方法，微分技术能部分消除低频光谱成分的影响。现在微分光谱已广泛地应用于研究植被的生物物理参数、矿物和有机质等。然而利用微分光谱对土壤水分反演的研究却鲜见报道。本文通过对实验室中多种不同类型的土壤进行光谱与土壤表层水分含量进行观测，探讨了通过土壤反射率与微分光谱对土壤表层水分的反演方法。4种类型的土壤光谱数据(反射率(R)，反射率倒数的对数(log(1／R))，反射率的一阶微分光谱(dR／dλ)，反射率倒数的对数的一阶微分光谱(d(log(1／R))／dλ))与土壤表层水分之间的关系在本文中得到分析，R与log(1／R)对于不同土壤类型与土壤表层水分都很敏感，说明通过R与log(1／R)反演土壤表层水分受土壤类型的影响很大，而dR／dλ，d(log(1／R))／dλ)对土壤类型却不敏感，对土壤表层水分较为敏感，说明dR／dλ和d(log(1／R))／dλ)对于反演不同类型土壤具有很大的潜力，微分光谱与土壤水分在某些波段具有显著的相关性。通过随机对9种土壤(各具有4个土壤水分)的数据建立反演土壤水分的模型，并其他9种土壤(各具有4个土壤水分)的数据进行验证模型，结果表明，dR／dλ和d(log(1／R))／dλ)能够显著提高R与log(1／R)对于不同土壤类型土壤表层水分的反演精度，由于吸收过程是非线性的，在四种类型的土壤光谱数据中，总体来说，d(log(1／R))／dλ)具有最好的能力预测不同类型土壤的表层水分含量。     

Dust production and the release of iron oxides resulting from the aeolian abrasion of natural dune sands

Global dust trajectories indicate that signi?cant quantities of aeolian‐transported iron oxides originate in contemporary dryland areas. One potential source is the iron‐rich clay coatings that characterize many sand‐sized particles in desert dune?elds. This paper uses laboratory experiments to determine the rate at which these coatings can be removed from dune sands by aeolian abrasion. The coatings impart a red colour to the grains to which previous researchers have assigned variable geomorphological signi?cance. The quantities of iron removed during a 120 hour abrasion experiment are small (99 mg kg^?1) and dif?cult to detect by eye; however, high resolution spectroscopy clearly indicates that ferric oxides are released during abrasion and the re?ectance of the particles alters. One of the products of aeolian abrasion is ?ne particles (<10 µm diameter) with the potential for long distance transport. Copyright © 2004 John Wiley & Sons, Ltd.     

Sorption of Eu~(3+) onto nano-size silica-water interfaces

A large amount of nuclear wastes has been pro-duced due to nuclear weapon development and nuclear electricity generation. One possible resolution for the disposal of the nuclear wastes is to seal them in an underground repository, which requires detailed knowledge on the mobility, chemical behavior and immobilization of radionuclides in underground water. In addition, toxic heavy metals are extensively present in ground and underground water, how to immobilize and remedy these toxic heavy meta…