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不同性味矿物药的特征元素组成 总被引：1，自引：0，他引：1
应用自适应模式识别的ＩＤ３方法，通过３０种和３６种矿物药模式，分别建立起矿物药的“性”与其溶出元素的种类及含量之间和矿物药的“味”与其溶出元素的种类及含量之间的一般关系．矿物药的性与Ｓｉ、Ｍｎ、Ａｌ、Ｓｒ的不同含量有关，矿物药的味与Ｃｕ、Ｆｅ、Ｍｎ、Ｃａ的不同含量有关．上述元素为决定矿物药性味的特征元素． 相似文献
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气溶胶粒子对城市夜间边界层温度影响的模式研究 总被引：3，自引：0，他引：3
用一维非定常模式模拟大气气溶胶粒子对城市夜间边界层大气温度场的影响。结果表明：气溶胶粒子对近地层大气地增温作用，对１５０ｍ以上大气起降温作用，并削弱近地逆温层的强度。 相似文献
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Le Zhang Jia‐Lin Wu Jia‐Run Tu Dan Wu Nan Li Xiao‐Ping Xia Zhong‐Yuan Ren 《Geostandards and Geoanalytical Research》2020,44(1):133-145
Matrix‐matched reference materials are necessary for accurate microbeam U‐Pb dating and Hf isotopic determination. This study introduces the RMJG rutile as a new potential reference material, which was separated from Palaeoproterozoic pelitic granulites collected in Hebei Province, China. LA‐ICP‐MS measurements indicate the RMJG rutile has extremely low Th (< 0.003 ± 0.01 µg g?1) and common Pb contents, but high Hf (102 ± 34 µg g?1), U (61 ± 11 µg g?1), and radiogenic Pb (~ 20 µg g?1) contents. Moreover, the rutile yields relatively constant U‐Pb ages and Hf isotopic data. The LA‐ICP‐MS analyses suggest that this rutile has a concordant U‐Pb age with a statistical mean 206Pb/238U and 207Pb/235U ages of 1749.9 ± 32.1 Ma and 1750.0 ± 26.4 Ma, respectively (2s), which are statistically indistinguishable from its ID‐TIMS ages (1750.6 ± 8.4 and 1750.1 ± 4.7 Ma). Precise determination of the 176Hf/177Hf ratio by MC‐ICP‐MS in solution mode (0.281652 ± 0.000006) is in good agreement with the statistical mean of the LA‐MC‐ICP‐MS measurements (0.28166 ± 0.00018). Therefore, the limited variations of RMJG U‐Pb age and Hf isotopic composition together with its extremely low common Pb and high Hf, U and Pb contents make it an ideal calibration and monitor reference material for LA‐ICP‐MS measurements. 相似文献
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主叫用户识别及其语音实现 总被引：1，自引：0，他引：1
介绍了主叫用户识别技术的基本原理 ,分析了其目前的几种实现方法 ,在此基础上提出了一种新颖的语音实现方案 ,给出了此方案的具体硬、软件设计 相似文献
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Characterisation of Apatites as Potential Uranium Reference Materials for Fission‐track Dating by LA‐ICP‐MS 
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下载免费PDF全文 Cleber J. Soares Regina Mertz‐Kraus Sandro Guedes Daniel F. Stockli Thomas Zack 《Geostandards and Geoanalytical Research》2015,39(3):305-313
We report homogeneity tests on large natural apatite crystals to evaluate their potential as U reference materials for apatite fission‐track (AFT) thermochronology by laser ablation‐inductively coupled plasma‐mass spectrometry (LA‐ICP‐MS). The homogeneity tests include the measurements of major element concentrations by electron probe microanalysis (EPMA), whereas for U concentration, isotope dilution (ID) ICP‐MS and laser ablation (LA) ICP‐MS were employed. Two apatite crystals are potential reference materials for LA‐ICP‐MS analysis: a 1 cm3 fraction of a Durango crystal (7.5 μg g?1 U) and a 1 cm3 Mud Tank crystal (6.9 μg g?1 U). The relative standard deviation (1 RSD) of the U concentration determined by ID‐ICP‐MS of both apatite crystals was ≤ 1.5%, whereas 1 RSD for the LA‐ICP‐MS results was better than 4%, providing sufficient homogeneity for fission‐track dating. The results on the U homogeneity for two different apatite samples are an important step towards establishing in situ dating routines for AFT analysis by LA‐ICP‐MS. 相似文献
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Yimin Wang Xiaohong Wang Wenjun Qu Yushu Gao Tiexin Gu Xingtao Fan S.I. Andreev Xuefa Shi 《Geostandards and Geoanalytical Research》2011,35(3):341-352
Two Co‐rich seamount crust reference materials, MCPt‐1 and MCPt‐2, were prepared using ultra‐fine particle size milling technique and characterised for the platinum‐group elements (PGEs). The raw material for these two reference materials was collected separately from the Magellan seamounts of the western Pacific Ocean and the seamounts of the central Pacific Ocean by Russian and Chinese scientists. First, they were ground by ball mill to a ?200 mesh powder, then further processed by ultra‐fine jet mill and well‐mixed. The particle size distributions of the samples were tested by a laser particle analyser; the average particle size was 1.8 and 1.5 μm (equal to about 2000 mesh) respectively. The homogeneity of six major and minor elements in these two materials was tested at the milligram level of sampling mass by high‐precision wavelength dispersive X‐ray fluorescence (XRF) spectrometry and at the microgram level of sampling mass by electron probe microanalyser. The homogeneity of more than forty trace elements, including Pt, was tested at the microgram level of sampling mass by LA‐ICP‐MS. Except for Rh, all PGEs were determined by isotope dilution‐ICP‐MS. Platinum in MCPt‐1 and MCPt‐2 was characterised as certified values, whereas the other five PGEs in MCPt‐1 and MCPt‐2 were reported as reference values. In addition, the information values of sixty‐two major, minor and trace elements were obtained by XRF, ICP‐AES and ICP‐MS. The minimum sampling mass for the determination of PGEs was 1 g, while the minimum sampling mass for the determination of the other elements was 2–5 mg. 相似文献
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提出并实现了一种中文姓名信息提取方法，该方法首先根据姓氏和名的用字概率信息，将姓氏作为抽取的触发条件，在文本中初步提取姓名。然后再充分利用中文姓名的上下文信息及姓名用字之间的关联程度的信息，选取特征作为决策树测试的属性列表，并将初步提取出来的姓名是否是真实姓名（bool型的值：yes或no）作为决策树要预测的目标属性，组建基于ID3算法的决策树进一步提取出正确的姓名，实验结果表明，该方法具有很好的召回率和准确率。 相似文献
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Que D. Hoang Tak Kunihiro Chie Sakaguchi Masahiro Yamanaka Hiroshi Kitagawa Eizo Nakamura 《Geostandards and Geoanalytical Research》2019,43(1):147-161
To precisely determine the abundances of fifty‐two elements found within natural water samples, with mass fractions down to fg g?1 level, we have developed a method which combines freeze‐drying pre‐concentration (FDC) and isotope dilution internal standardisation (ID‐IS). By sublimation of H2O, the sample solution was reduced to < 1/50 of the original volume. To determine element abundance with accuracy better than 10%, we found that for solutions being analysed by mass spectrometry the HNO3 concentration should be > 0.3 mol l?1 to avoid hydrolysis. Matrix‐affected signal suppression was not significant for the solutions with NaCl concentrations lower than 0.2 and 0.1 cg g?1 for quadrupole ICP‐MS and sector field ICP‐MS, respectively. The recovery yields of elements after FDC were 97–105%. The detection limits for the sample solutions prepared by FDC were ≤ 10 pg g?1, except for Na, K and Ca. Blanks prepared using FDC were at pg‐levels, except for eleven elements (Na, Mg, Al, P, Ca, Mn, Fe, Co, Ni, Cu and Zn). The abundances of fifty‐two elements in bottled drinking water were determined from five different geological sources with mass fractions ranging from the fg g?1 to μg g?1 level with high accuracy. 相似文献