喉癌CT分型和CD44V6表达的意义     

孙伟英  袁建华  施明英 《CT理论与应用研究》2002,11(1):17-19

目的 探讨喉癌的CT分型和转移相关因子CD44V6表达的意义。方法 对39例喉鳞癌行术前常规CT检查，其术后标本进行CD44V6的表达检测，与术前CT片作对照分析。结果39例喉鳞癌CT检查；声门型24例，声门上型14例，跨声门型1例，声门下型0例；T1－2级22例，T3－4级17例；淋巴结转移组13例，非转移组26例，CD44V6总的阳性表达率为61．5％，对各组均采用秩次检验分析，CD44V6在喉癌的CT的T分级和淋巴结分组中存在显著性差异（P＜0．01）。而部位分区无明显差异。结论 喉癌的CT分型中的T分级、淋巴结分组与CD44V6的阳性表达密切相关。  相似文献   

硬玉的差热分析和紫外荧光光谱研究   总被引：2，自引：0，他引：2  

彭卓伦  彭明生  徐庆鸿 《矿产与地质》2003,17(5):630-631,635

通过对缅甸硬玉的差热分析和紫外荧光光谱研究，发现不同颜色硬玉的紫外荧光谱中的617nm处的谱峰，可能是Cr引起的；对不同颜色硬玉进行的差热分析表明，其熔融温度略有不同，说明其生长环境有一定差异，而硬玉也可能是较好的耐热材料，具一定的开发潜能。  相似文献   

ARL9400型X荧光光谱仪探测器高压部分故障分析与维修     

吴红旗 《岩矿测试》2003,22(4):307-309

简述了瑞士ARL 9400型X荧光光谱仪探测器高压部分的故障现象、分析与处理及维修方法，并给出了维修实例。  相似文献   

原子荧光光谱法测定芦荟中砷和硒   总被引：5，自引：1，他引：5       下载免费PDF全文

林章金 《岩矿测试》2003,22(3):237-238

应用AFS 820型双道原子荧光仪测定芦荟中砷和硒,方法检出限分别为As0.51μg/L;Se0.42μg/L。经国家一级植物标准物质分析验证,结果与标准值相符。5次测定相对标准偏差As<2.3%;Se<3.1%。  相似文献   

原子荧光光谱法测定化探样品时有机质对As,Sb,Bi的干扰   总被引：1，自引：0，他引：1  

汪明启  刘应汉 《地质科技情报》2003,22(1):105-109

通过研究黑龙江省森林沼泽景观区有机水系沉积物（泥炭）、土壤中As,Sb,Bi的测定结果，发现样品中的有机质对王水消解氢化物原子荧光法测定上述元素存在极大的干扰，提出采用低温（＜450℃）灰化处理可完全消除干扰。对比研究还发现，过去森林沼泽景观区的区域化探扫面资料中的As,Sb,Bi数据存在问题，应专门对其进行评价研究。  相似文献   

Enhanced red fluorescence emission in the oxygen minimum zone of the Arabian Sea     

Wiebke Breves  Rüdiger Heuermann  Rainer Reuter 《Ocean Dynamics》2003,53(2):86-97

 Depth profiles of fluorescence at several excitation and emission wavelengths were measured along with CTD data during the cruise So119 of RV Sonne in the Arabian Sea from 12 May to 10 June 1997. In addition to chlorophyll fluorescence from phytoplankton in the near-surface layer, the profiles in the oxygen minimum region well below the euphotic zone show enhanced red fluorescence. Red fluorescence intensity is inversely related to the oxygen concentration in intermediate and deep waters. A relationship to characteristic water masses of the region cannot be found in the data, and this holds also with chemical data such as DOC. Absorbance spectra of water samples taken in the oxygen minimum zone show an absorption band at 420 nm wavelength with about 50 nm bandwidth, much weaker than gelbstoff absorbance in the same wavelength range. The absorption band remains stable after sample filtration with 0.45 μm glass fibre filters. Hence, the size of the absorbing matter is in the range of dissolved molecules or particles much smaller than 1 μm. Fluorescence spectra of unfiltered samples with 420 nm excitation show a weak emission band at 600 nm and a more pronounced one at 660 nm wavelength. The trailing edge of the 660 nm band falls into the range of chlorophyll emission, thus giving rise to the observed depth profiles of red fluorescence in the oxygen minimum zone. Red fluorescence measured on samples remain stable during a few hours after sampling even in the presence of oxygen. It is not detectable after several weeks of sample storage in the dark and cannot be reproduced even after depletion of dissolved oxygen. Received: 22 May 2002 / Accepted: 18 February 2003 Responsible Editor: Andreas Oschlies Acknowledgements. This work was supported by a grant from the Federal Minister of Education and Technology, Bonn, within the frame work of the JGOFS Arabian Sea program. We are grateful to the captain and the crew of RV Sonne for their support. We are indebted to Mrs. Kirsten Neumann from the Institute of Marine Chemistry and Biogeochemistry of the University of Hamburg for providing the oxygen data, and to Mr. Nikolai Delling from the same institute for making the DOC and chlorophyll data available to us.  相似文献   

Raman scattering and X-ray diffraction study of the thermal decomposition of an ettringite-group crystal     

S. K. Deb  M. H. Manghnani  K. Ross  R. A. Livingston  P. J. M. Monteiro 《Physics and Chemistry of Minerals》2003,30(1):31-38

 A Raman scattering and X-ray diffraction study of the thermal decomposition of a naturally occurring, ettringite-group crystal is presented. Raman spectra, recorded with increasing temperature, indicate that the thermal decomposition begins at ≈55 °C, accompanied by dehydration of water molecules from the mineral. This is in contrast to previous studies that reported higher temperature breakdown of ettringite. The dehydration is completed by 175 °C and this results in total collapse of the crystalline structure and the material becomes amorphous. The Raman scattering results are supported by X-ray diffraction results obtained at increasing temperatures. Received: 9 July 2001 / Accepted: 14 August 2002  相似文献   

Advances in energy-dispersive X-ray fluorescence   总被引：1，自引：0，他引：1  

Utz Kramar 《Journal of Geochemical Exploration》1997,58(1):73-80

Recently, two new instruments for X-ray fluorescence analysis (XRF) with interesting features for geochemical applications came to the market. Both instruments were designed to improve the peak to background ratio, the principal factor limiting the sensitivity of XRF. Total reflection XRF (TXRF) was designed to analyse extremely small sample amounts. An instrument, using polarised X-rays (P-XRF) for excitation, is designed to reduce scattered background in spectra of bulk samples. The performance of both instruments was compared with conventional XRF-methods and ICP/MS. Results for GXR-1, GXR-2, GXR-3, GXR-4 and GXR-6 obtained with TXRF and P-XRF are in good agreement with literature data. The effective amount of sample, analysed by TXRF was 200 μg only and detection limits of ~ l μg/g were achieved. P-XRF shows considerable improved detection limits (0.25–0.5 μg/g) for bulk samples for elements with atomic numbers 42–51 (Mo-Sb) compared with conventional XRF-methods.  相似文献   

X射线荧光测井井液的影响与校正     

葛良全  周四春  谢庭周  章晔  程业勋  侯胜利 《物探化探计算技术》1996,(S5)

X射线荧光测井中 ,井液位于井下探管与井壁之间 ,它的影响不但表现在对特征X射线的吸收 ,而且表现在对源初级射线和特征 X射线的散射。井液的校正采用硬件与软件相结合的方法 ,在硬件上 ,使含有探测器的部分制成单独的短臂 ,有效地保证了探测窗与井壁的良好接触 ;在软件上 ,提出的双散射峰法和散射峰 -逃逸峰法 ,能够校正 0 - 10 mm厚的井液对 X射线荧光测井结果的影响  相似文献   

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

A. N. Buckley  R. N. Lamb 《International Journal of Coal Geology》1996,32(1-4)

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.  相似文献