松辽盆地东南部油气、煤层气后生蚀变硫同位素特征

对松辽盆地东南部上白垩统泉头组、姚家组和嫩江组岩石中黄铁矿及硫同位素特征研究表明,泉头组、姚家组中后生还原褪色作用形成的灰色、灰绿色砂岩中的黄铁矿及硫同位素均显示出了深部来源的油气、煤层气有机流体作用成分特征。该区原生沉积成岩岩石及黄铁矿中硫同位素的δ^34SV-CDT为正值,油气、煤层气有机流体还原作用岩石及黄铁矿中δ^34SV-CDT为负值。油气、煤层气还原作用不仅使杂色、紫红色原生氧化砂岩还原为灰色、灰绿色还原性砂岩,还使岩石还原容量大大增强,而且油气、煤层气在有机流体与岩石的相互作用过程中有铀的叠加富集,岩石铀含量普遍增加,局部可形成铀异常、铀矿化。首次在门达地区姚家组含矿砂岩中发现网脉状水云母化,显示铀成矿具有低温热液蚀变特征,铀矿化与低温热流体作用有关。     

云南兰坪盆地北部东缘铅锌矿床喷流沉积成因的厘定———来自矿物学和硫同位素证据

通过详细的野外地质工作和显微镜下观察,对云南兰坪盆地东北部维西—乔后断裂带上三叠统石钟山组(T₃s)中产出的铅锌矿床成因进行厘定。研究结果表明,测区内存在大量典型的同生沉积矿床标志,如:纹层构造、条纹条带构造、网脉构造、黄铁矿条带软沉积构造、黄铁矿草莓状结构、黄铁矿胶状构造、闪锌矿同心环状构造等。青甸湾矿床金属硫化物硫同位素测试结果显示,黄铁矿的δ34 S介于3.7‰ ~ 8.1‰,均值5.34‰; 闪锌矿的δ34 S介于5.2‰ ~ 10.0‰之间,均值为7.18‰; 方铅矿的δ34 S介于5.2‰ ~ 9.9‰之间,均值为7.275‰,铅锌矿床硫来源于海水硫酸根无机还原。结合矿床形成时代及大地构造背景,认为该区铅锌矿为喷流沉积作用形成。      

Sulfur Determination in Geological Samples Based on Coupled Analytical Techniques: Electric Furnace-IC and TGA-EGA

A study has been undertaken to determine sulfur in geological samples by coupled analytical techniques. Two measurement methods have been developed: one using an electric furnace coupled to an ion chromatograph (electric furnace-IC) and another using infrared (IR) and quadrupole mass spectrometry (QMS) for evolved gas analysis (EGA) coupled with a thermogravimetric analyser (TGA). In the electric furnace-IC method, measurement was performed without any sample pre-treatment. The measurement conditions were optimised by varying sample quantity, type of catalyst (WO₃, Cu, W and V₂O₅) and sample/catalyst ratio, and the detection limit was 10 μg g⁻¹. Sulfur ores decompose at different temperatures. However, TGA-EGA allowed identification of the different forms of sulfur in the sample, even when they were found in very low concentrations, because the sulfur was continuously analysed. The developed chromatographic method allowed simultaneous analysis of several sample components, such as S, Cl and F, with a low detection limit. The method was much faster and more specific than the methods described in the literature. The results of the sulfur determination had low scatter, possibly because the samples underwent little handling during analysis: the operator only weighed and placed the sample in the furnace, the rest of the measurement process was fully automated. The results obtained by both the developed methods have been validated by using reference materials and comparison with combustion-IR spectroscopy, a standard method for determining total sulfur in a sample.     

On the scavenging of SO2 by cloud and raindrops: II. An experimental study of SO2 absorption and desorption for water drops in air

For the purpose of testing our previously described theory of SO₂ scavenging a laboratory investigation was carried out in the UCLA 33 m long rainshaft. Drops with radii between 250 and 2500 m were allowed to come to terminal velocity, after which they passed through a chamber of variable length filled with various SO₂ concentrations in air. After falling through a gas separating chamber consisting of a fluorocarbon gas the drops were collected and analyzed for their total S content in order to determine the rate of SO ₂ absorption.The SO₂ concentration in air studied ranged between 1 and 60% (v). Such relatively large concentrations were necessary due to the short times the drops were exposed to SO₂ in the present setup. The present experimental results were therefore not used to simulate atmospheric conditions but rather to test our previously derived theory which is applicable to any laboratory or atmospheric condition. Comparison of our studies with the results from our theory applied to our laboratory conditions led to predicted values for the S concentration in the drops which agreed well with those observed if the drops had radii smaller than 500 m. In order to obtain agreement between predicted and observed S concentrations in larger drops, an empirically derived eddy diffusivity for SO₂ in water had to be included in the theory to take into account the effect of turbulent mixing inside such large drops.In a subsequent set of experiments, drops initially saturated with S (IV) were allowed to fall through S-free air to determine the rate of SO ₂ desorption. The results of these studies also agreed well with the results of our theoretical model, thus justifying the reversibility assumption made in our theoretical models.In a final set of experiments, the effects of oxidation on SO₂ absorption was studied by means of drops containing various amounts of H₂O₂. For comparable exposure times to SO₂, the S concentration in drops with H₂O₂ was found to be up to 10 times higher than the concentration in drops in which no oxidation occurred.     

三次拟合计算法测定土壤样品中的硫含量

本方法采用三次拟合计算法处理土壤样品中硫含量的测试结果。试样采用传统的燃烧碘量法进行处理,在结果计算中使用三次拟合法处理测试结果,取得令人满意的效果。本方法的精密度为1.54%5.38%,方法检出限（3S）：0.005%,较好的满足土壤样品中硫的测试要求。     

赣南崇义淘锡坑钨矿床氢、氧、硫同位素地球化学研究

赣南崇义县淘锡坑钨矿位于南岭东西向构造带东段与武夷山NE-NNE向构造带南段的复合部位,属于以石英脉型黑钨矿为主的钨多金属矿床.文章通过氧、氧、硫同位素地球化学特征的研究,探讨了淘锡坑钨矿成矿流体的来源及演化.研究结果显示:δD值介于-77‰～-45‰之间;石英矿物的δ18O值介于+7.3‰～+12.2‰之间,计算给出...     

Sulfur Isotopes of Framboidal Pyrite in the Permian-Triassic Boundary Clay at Meishan Section

Pyrite framboids were found in the Permian-Triassic boundary at Meishan Section, while their sulfur isotopes were determined. The majority of framboids is less than 5 μm in diameter, with some large-sized framboids. Also, euhedral gypsums were observed in the boundary clay. The authors suppose that most of the pyrite framboids formed just below the redox boundary and stopped growing after entering the lower water column. The result indicates that it was probably lower dysoxia condition in the temporal ocean. Moreover, the authors also presume that some pyrite was oxidated to sulfates accompanying the fluctuation of redox condition, which would probably be the origin of the negative sulfur isotopes of gypsum and CAS reported before. In addition, sulfur isotope of framboidal pyrite suggests that sulfur is originated from bacterial sulfate reduction in anoxic condition. Therefore, this study confirms that the ocean was widely anoxic during the Permian-Triassic transitional period. However, the redox condition in temporal ocean was probably not stable, with short-term fluctuations.     

贵州纳雍水东铅锌矿矿床地球化学特征

对贵州纳雍水东乡洗米沟、坟山脚一带灯影组地层中铅锌矿石采样,进行镜下观察和全岩主量、微量元素、稀土元素以及硫同位素地球化学研究。微量元素研究表明,矿床中N i、Mo、As、Sb等成矿元素富集明显,Sr、Ba、V等元素强烈亏损,认为早寒武世热水对铅锌矿源层进行了淋滤和改造;稀土元素研究表明,铅锌矿石稀土配分曲线向右倾斜,...     

川东北地区海相烃源岩中单质硫的定性与定量分析

利用定性与定量分析手段,研究了川东北地区各类海相烃源岩中的单质硫及其地球化学特征。定性分析表明,该区海相烃源岩中的单质硫具有八硫环状结构和六硫状环结构两种晶体构型,由S8和S6两种同素异形体组成,其中S8具有相对较高的丰度。定量分析表明,该区海相烃源岩中的单质硫含量为0.91×10-6～375.88×10-6,具有很宽的分布范围,并且随着烃源岩分布区域、地层时代以及岩性的不同而发生明显变化,表现出强烈的非均质性分布特征。该区海相烃源岩中单质硫含量与有机碳含量之间存在正相关关系,说明单质硫主要发育在富有机质沉积的层段中。通过单质硫含量与总硫含量对比分析,间接证明了川东北地区各类海相烃源岩中赋存有丰富的有机含硫化合物。     

翠宏山铁多金属矿床成矿流体包裹体及硫同位素特征

对翠宏山铁多金属矿床成矿早期阶段钨钼矿体中的石英、成矿晚期阶段铅、锌、铜矿体中的萤石流体包裹体特征及均一温度、盐度的研究表明,从早期钨钼成矿阶段至晚期铅、锌、铜成矿阶段,侵入体内接触带至外接触带,经历了一个温度剧降和盐度显著增加的过程。钨钼成矿阶段成矿流体主要为岩浆热液流体,成矿过程为单一的成矿流体冷却过程; 在晚期铅、锌、铜成矿阶段,来自岩浆中的温度较高的热流体与围岩地层中的大气降水等低温、高盐度流体混合,使成矿流体温度剧降和盐度增高,导致铅、锌、铜等成矿物质的沉淀。辉钼矿和方铅矿的δ34S ( × 10-3 ) 测试结果表明,侵入体内接触带钨钼矿体的成矿物质主要来自岩浆热液; 围岩地层中铅、锌、铜矿体的成矿物质,除岩浆热液来源外,部分可能来自雨水对地层中硫酸盐岩中硫及其他成矿物质的淋滤。