微波炉在重量法测定硫中的应用     

姜锋  江荣燕 《岩矿测试》1993,12(2):135-136

采用玻璃砂芯坩埚过滤BaSO_4沉淀,微波炉代替马弗炉恒重坩埚、沉淀,重量法测定了矿石中的硫。方法准确,精密度好。微波炉不需预先升温,加热6min可达恒重,省时、省电。  相似文献   

淄博煤矿矿坑排水对地表水体的污染及对地下水水质影响的研究   总被引：3，自引：0，他引：3  

钟佐燊  汤鸣皋  张建立 《地学前缘》1999,6(Z1):238-244

以山东淄博煤田富硫煤（w（St＞2％）煤矿作为典型研究区,阐述了由于直接排放酸性、高SO4离子、高硬度和较高矿化度（TDS）的矿坑水导致的地表水体及地下水的污染。研究区内地表水体的水质主要受控于矿坑排水的质量,区内主要河流、水库已被污染。引用这种受污染的地表水进行灌溉,会引起浅层地下水的严重污染,并影响到饮用此类地下水的人们的身体健康。为揭示污水灌溉过程中水-岩相互作用及地下水污染的机理,进行了现场土柱模拟实验,分别模拟了污水灌溉和降水入渗过程。实验结果表明,污水灌溉过程中SO4-不会被吸附,也不会产生沉淀,因此,污水灌溉是污灌区地下水受污染的主要原因。降水入渗实验表明,污灌区土壤中的SO4-,Ca2+和Mg2+,也可以通过降水淋滤进入地下水,这是污灌区地下水受污染的另一条途径。就对水环境的影响而言,酸性煤矿矿坑排水的环境效应是负面的,应予以高度重视。  相似文献   

融入WTO——为农业服务的化工矿产资源发展战略构想     

姜树叶  王炳铨  王君 《化工矿产地质》2002,24(4):193-197

我国直接为农业服务的磷、硫、钾矿资源总体形势不容乐观。针对各自资源特点,应采取不同的发展战略:磷——立足国内,有进有出,南出北进;硫——立足国内,适当进口,调整结构,必要储备;钾——稳定进口,国外开发,国内开发,国内找矿,四位一体,分三步走。为此建议:将磷、硫、钾纳入战略性矿产资源的范畴进行管理和规划;强化地勘队伍,加大找矿力度;增加投入,寻求新的突破;加大“走出去”的步伐;规范进出口秩序;国家在更高的层面进行宏观调控;拓宽为农业服务的新领域。  相似文献   

阿尔泰地区铜镍矿床综合信息找矿模型及成矿预测     

杨永强  范继璋  程丽红 《吉林大学学报(地球科学版)》2000,30(2):157-160

阿尔泰地区存在 5条与深大断裂有关的基性、超基性岩带 ,是铜镍硫化物矿床产出的有利地段 ,其中喀拉通克铜镍矿是我国大型铜镍矿之一。通过对成矿必要条件的深入研究 ,得出深大断裂及其次级断裂控制了岩体的产出 ,北北西向断裂叠加北西向断裂控制了矿体的产出 ;成矿充分条件是基性、超基性岩体 ,总结了岩体含矿性的评价指标。结合重磁及地化资料 ,在喀拉通克铜镍矿的成矿模式基础上 ,建立了区域综合信息找矿模型 ,进行成矿预测 ,圈定靶区 9处。  相似文献   

四川巴塘夏塞花岗岩和银多金属矿床年龄及ち颉⑶ν位素组成     

应汉龙  王登红  付小方 《矿床地质》2006,25(2):135-146

为了解四川西部夏塞银多金属矿区黑云母二长花岗岩形成和矿化发生的时代及成矿物质来源,测定了该矿区绒依措和若洛隆花岗岩的Rb_Sr年龄和钾长石、黑云母及主要银矿化阶段石英的40Ar/39Ar年龄及矿石的硫、铅同位素组成。花岗岩的结晶年龄约为93Ma,银矿化年龄约为75Ma。矿石硫可能源于花岗岩,但不能排除源于弱沉积围岩的可能性;矿石、花岗岩和弱变质沉积围岩的铅同位素组成相似,铅主要源于上地壳,少量源于下地壳。  相似文献   

胶东金矿集区硫和碳的循环与控矿作用     

孙林  杨斌  郭建军  杨开春 《矿产与地质》2006,20(2):97-101

胶东金矿集区矿石中普遍含金属硫化物和碳酸盐矿物,某些矿床中还见有富含炭质的断裂破碎带.成矿溶液中含有大量的SO4^2-、HCO3^-、CO2和有机质等的含硫和含碳组分.矿石硫同位素组成明显富集重硫,结合胶东金矿主要成矿时期（早白垩世）特殊的地质背景、同期海水硫酸盐δ^34S平均值（约＋16‰）及现代海水沿NE-NNE向断裂倒灌情况,笔者认为,硫的主要来源与海水硫的大量补给有关.而根据碳、氧同位素组成特征分析,形成金矿床中方解石的物源有很大一部分来自前寒武系碳酸盐岩.浅表环境下成矿金属元素及硫、碳等物质在热液对流系统中的大规模循环是成矿的关键,SO4^2-与S2^-之间的临界转化是制约成矿金属元素活化-迁移-聚集的重要因素,而含碳组分（CO3^2-、HCO3^-、CO2和有机质）则有利于Au、Cu、Pb、Zn等元素的活化和迁移,含硫和含碳组分的循环及有关的物理化学反应之间有明显的关联性.  相似文献   

The Atmospheric Oxidation of the HS Radical: Reaction with NO2     

Stella M. Resende 《Journal of Atmospheric Chemistry》2007,56(1):21-32

The atmospheric reaction between HS and NO₂ was theoretically investigated at 298 K and 1 atm of pressure. Our results show that the first reaction step will lead to the formation of HSNO₂ or HSONO, spontaneously and exothermically. HSONO easily decomposes into HSO + NO. On the other hand, HSNO₂ can hardly dissociate in the reactants, and its isomerization to other adducts is much hindered. Production of HNO + SO and SNO + OH was found to be unfavorable. Thus, the main products would be HSO + NO and HSNO₂, and new investigations focusing on the atmospheric fate of HSNO₂ are suggested. A general discussion of the fate of HS under atmospheric conditions is presented. Recent investigations indicate that NO₂, O₂ and N₂O should be the most important oxidants of HS, while the O₃ influence will not be significant.  相似文献   

热解硫酸钡制备硫同位素分析试样二氧化硫   总被引：1，自引：1，他引：0  

白瑞梅  李金城 《岩矿测试》1998,17(1):40-43

改进了硫同位素分析中由ＢａＳＯ４制备ＳＯ２的方法：ＢａＳＯ４和Ｖ２Ｏ５及ＳｉＯ２混合后覆盖铜丝,在真空状态９８０℃加热２０ｍｉｎ,用液氮捕集ＳＯ２。与火焰直接加热分解法相比,用高温炉方便,改善了制样环境,避免污染。经国际标样和国家标准物质分析验证,结果与标准值相符,标准偏差（１σ）在±００９‰～±０２０‰,符合分析要求。  相似文献   

A Three-Dimensional Global Model Study of Carbonyl Sulfide in the Troposphere and the Lower Stratosphere   总被引：4，自引：0，他引：4  

Erik Kjellström 《Journal of Atmospheric Chemistry》1998,29(2):151-177

Global distributions of carbonyl sulfide and carbon disulfide have been calculated with a three-dimensional global model of the atmospheric general circulation (ECHAM). The model calculates a global sink strength for carbonyl sulfide of 0.3 Tg S yr^-1, with vegetation uptake being the largest sink. With this sink strength, the sources have to be close to the lower limit of the present estimate in the literature. The calculated mixing ratios are higher in the Southern Hemisphere than in the Northern Hemisphere. This interhemispheric gradient is the opposite of what is observed demonstrating that the present knowledge of the distribution of sinks and sources is not fully adequate. The model calculations support the idea that the open oceans could act as a net sink of carbonyl sulfide. The calculated stratospheric photolysis of carbonyl sulfide constitutes about 4% of the total sink of carbonyl sulfide. A stratospheric production of sulfate from carbonyl sulfide of 0.013 Tg S yr^-1 is obtained, which is 3 to 12 times less than what is needed to maintain the stratospheric sulfate aerosol layer. Although these results are associated with uncertainties, due to the low upper boundary and coarse vertical resolution of the model, they support recent findings of a low stratospheric production of sulfate from carbonyl sulfide. Instead, sulfur dioxide transported from the troposphere is calculated to be the most important precursor for the stratospheric sulfate aerosol layer.  相似文献   

Model Simulations on the Variability of Particulate MSA to Non-Sea-Salt Sulfate Ratio in the Marine Environment     

Veli-Matti Kerminen  Risto E. Hillamo  Anthony S. Wexler 《Journal of Atmospheric Chemistry》1998,30(3):345-370

A box model was constructed to investigate connections between the particulate MSA to non-sea-salt sulfate ratio, R, and DMS chemistry in a clean marine boundary layer. The simulations demonstrated that R varies widely with particle size, which must be taken into account when interpreting field measurements or comparing them with each other. In addition to DMS gas-phase chemistry, R in the submicron size range was shown to be sensitive to the factors dictating sulfate production via cloud processing, to the removal of SO₂ from the boundary layer by dry deposition and sea-salt oxidation, to the entrainment of SO₂ from the free troposphere, to the relative concentration of sub- and supermicron particles, and to meteorology. Three potential explanations for the increase of R toward high-latitudes during the summer were found: larger MSA yields from DMS oxidation at high latitudes, larger DMSO yields from DMS oxidation followed by the conversion of DMSO to MSA at high latitudes, or lower ambient H₂O₂ concentrations at high latitudes leading to less efficient sulfate production in clouds. Possible reasons for the large seasonal amplitude of R at mid and high latitudes include seasonal changes in the partitioning of DMS oxidation to the OH and NO₃ initiated pathways, seasonal changes in the concentration of species participating the DMS-OH reaction pathway, or the existence of a SO₂ source other than DMS oxidation in the marine boundary layer. Even small anthropogenic perturbations were shown to have a potential to alter the MSA to non-sea-salt sulfate ratio.  相似文献