遥感筛选评价区化异常的初步探索

近年来,作者发展了七种以上重要找矿指示元素的野外快速分析法,此乃其一。文中提出一种新的金样冷浸技术,引进了新的光导光度检测方法,样品经溴化钠—硫酸—过氧化氢冷浸,用经丙酮—MIBK处理的泡沫塑料富集金,经混合解脱剂解脱并直接取解脱液用改进的微珠析出法或用光导光度法测定。取10g样品,可测定0．0005- 50g/t范围内的金。方法简便、快速,可在普查分队驻地进行,每一工作日可测定80多个样品,由于废弃了王水分解样品和泡沫塑料的灰化,具有广阔的应用前景。     

矿石中金的在线固相萃取及缝管火焰原子吸收测定

介绍了将流动注射在线因相萃取预浓集与石英缝管火焰原子吸收相结合测定矿石中金的方法，用ＸＡＤ－８吸附树脂填充的微型柱（１００μｌ）在６ｍｌ／ｍｉｎ的流速下，从０．５ｍｏｌ／ＬＨＣｌ介质的试样溶液中浓集金氯络合物，再用乙醇洗脱，最后由火焰原子吸收检测，在采样频率为１０３样／ｈ的流速下灵敏度提高４７倍，分析精度为１．３％，检出限为１．０μｇ／Ｌ；在６５样／ｈ的采样频率下灵敏度提高９５倍，检出限可达０．７     

Determination of part-per-trillion levels of atmospheric dimethyl sulfide by isotope dilution gas chromatography/mass spectrometry

Stable isotopic dilution was applied to the determination of dimethyl sulfide (DMS) in ambient air at the low part-per-trillion by volume (pptrv) levels. Perdeuterated DMS was used as an internal standard in the gas chromatography/mass spectrometry determination. The isotopically labelled internal standard provided insensitivity to possible losses of DMS in sampling and analysis. The lower limit of detection (LLD) was 1 pptrv with a sample acquisition time of 2 min.     

Chemistry of alkali extraction of brown coals—I. Kinetics, characterisation and implications to coalification

Three Australian brown coals have been separated into humin and humic acid fractions and studied by high resolution solid state ¹³C NMR spectroscopy and Fourier transform IR spectroscopy. The aromatic rings of the humic acids are highly substituted showing that extensive cross linking must have occurred during formation from wood lignin and tannin. However, the humins contain more aliphatic carbon and hydrogen than the corresponding humic acids. This shows that little cross linking has occurred with other components of the brown coal such as resins, waxes cutin and algal detritus, and cross linking has not rendered the aromatics alkali insoluble. The kinetics of extraction are complex and not simple first order. This is reflected in the chemical composition of the humic acid which is extraction temperature dependent. We also observed that there is a conversion of aromatic carbon to aliphatic carbon and gas during extraction, probably by alkaline oxidation, resulting in ring opening. A range of suitable model compounds have been studied to confirm this finding. Such a mechanism may account for the modification of lignin in oxidising environments such as those occurring in the initial stages of coalification (lignite or brown coal formation) and in soils.     

离子色谱—双电导法同时测定水样中多种阴离子的研究

本文在Dionex2020i离子色谱仪上,选用0.61×10~(-3)mol/L NaHCO_3-1.61×10~(-3)mol/LNa_2CO_3水溶液作淋洗液,在HPIC-AS4A阴离子分离柱上分离痕量F~-、NO_2~-、Br~-和较高浓度的Cl~-、NO_3~-、SO_4~(2-);选用2.0×10~(-3)mol/L TBAOH-6％CH_3CN水溶液作淋洗液,在MPIC-NS1分离柱上分离痕量F~-、Br~-和较高浓度的Cl~-,然后用串联双电导检测器的不同输出范围分别同时定量测定。本法特别适用于相邻两种离子浓度相差较大,前面高含量的离子对后面痕量离子测定有干扰的样品。用本文拟定的HPIC方法测定除铬后的地下水样中多种阴离子的结果与文献值吻合。     

遥感特征信息提取的综合分析——以红外细分波段新疆铁木尔特航带矿化特征信息提取为例

本文以红外细分波段新疆铁木尔特航带为例,依据不同地质体各自的光谱特征,运用主成分分析、多种信息复合等技术与综合分析方法,使该地段的矿化特征提取收到了良好效果。 本航带的矿化特征信息在图像处理结果中表现为黄色异常色调。它反映了当地多金属成矿带中二氧化硅含量低、全铁含量较高的岩矿矿化特征。团块状黄色异常色调表示出地表出露的铁帽、磁铁矿化和矽卡岩化的分布状况。野外验证表明,黄色调的分布地域与实地的地表矿化范围相吻合。 遥感特征信息提取的综合分析方法包括信息基本特征分析、图像处理、后验分析和机理解释等四个相互联系的步骤。研究表明,只有经过综合分析,才能揭示出特征信息的内在规律性,使特征信息具有较好的实用价值。     

固态萃取光度法测定痕量钛

本文采用熔融联苯萃取8-羟基喹啉钛,继后溶固相于N,N-二甲基甲酰胺中,在390nm处测量吸光度。实验确定了各参数的最佳值,其摩尔吸光系数为7.9×10~3L·mol~(-1)·cm~(-1),一些干扰元素可以掩蔽。方法迅速、简便,用于测定铍铜合金中的痕量Ti,所得结果令人满意.     

北京平原区基岩井水位的年动态特征及其成因分析

系统阐述了北京平原区１０口地震地下水位动态观测井及其水位年动态特征，主要分析了降雨与开采对年动态特征的影响，讨论了大同－阳高地震前后某些井水位长期异常的信度     

基于松弛法的影像边缘提取

提出一种基于松弛法的影像边缘提取算法．本文详述了边缘标号的设置及初始概率的计算，并根据邻域内的信息分布，综合考虑了边缘的先验知识，设计出自适应的支持函数．     

A comparison of the early diagenetic environment in intertidal sands and muds of the Manukau Harbour,New Zealand

The early diagenetic environment of intertidal sandy sediments (sands) and muddy sediments (muds) is described and compared from two cores taken from an unpolluted part of the Manukau Harbour, New Zealand. Extraction techniques characterized the form of the trace elements (Fe, Mn, S, C, Pb, Zn, Cu) at different depths in the sediment. Dissolved forms of Fe, Mn, and S were measured in interstitial water. Nonresidual metal concentrations, humic acid, FeS, and FeS₂ are an order of magnitude higher in the muds than in the sands because of dilution by unreactive sand particles. Muds contain a larger proportion of metals in the mobile fractions; exchangeable (Mn), carbonate (Mn, Fe, Zn), and easily-reducible oxide (Fe, Mn, Zn, Pb). This is due to greater surface area (for Mn adsorption); the favorable conditions for MnCO₃, FeCO₃, and FeS precipitation; and higher concentrations of easily reducible iron oxide and humic acid. Therefore, compared to the sands, muds are more important as reservoirs for toxic metals, both in terms of quantity and availability. At either site there was very little difference between the forms of Zn, Pb or Cu identified by sequential extraction as sediments changed from oxic to anoxic conditions. One reason for this is that the amounts and proportions of some of the important components that bind metals, viz., amorphous iron hydrous oxides, humic acids, and FeS₂, do not change much. Other components that do change with redox conditions, for example, manganese phases and FeS, are only minor components of the sediment. Redox conditions, then, have relatively little effect on trace-metal partitioning in the sediment matrix of these unpolluted sediments.