Hydrogen sulfide measurements in air by passive/diffusive samplers and high-frequency analyzer: A critical comparison     

《Applied Geochemistry》2016

In this study, hydrogen sulfide (H₂S) measurements in air carried out using (a) passive/diffusive samplers (Radiello^® traps) and (b) a high-frequency (60 s) real-time analyzer (Thermo^® 450i) were compared in order to evaluate advantages and limitations of the two techniques. Four different sites in urban environments (Florence, Italy) and two volcanic areas characterized by intense degassing of H₂S-rich fluids (Campi Flegrei and Vulcano Island, Italy) were selected for such measurements. The concentrations of H₂S generally varied over 5 orders of magnitude (from 10⁻¹–10³ μg/m³), the H₂S values measured with the Radiello^® traps (H₂S_R) being significantly higher than the average values measured by the Thermo^® 450i during the trap exposure (H₂S_Ta), especially when H₂S was <30 μg/m³. To test the reproducibility of the Radiello^® traps, 8 passive/diffusive samplers were contemporaneously deployed within an 0.2 m² area in an H₂S-contaminated site at Mt. Amiata (Tuscany, Italy), revealing that the precision of the H₂S_R values was ±49%. This large uncertainty, whose cause was not recognizable, is to be added to that related to the environmental conditions (wind speed and direction, humidity, temperature), which are known to strongly affect passive measurements. The Thermo^® 450i analyzer measurements highlighted the occurrence of short-term temporal variations of the H₂S concentrations, with peak values (up to 5732 μg/m³) potentially harmful to the human health. The Radiello^® traps were not able to detect such temporal variability due to their large exposure time. The disagreement between the H₂S_R and H₂S_Ta values poses severe concerns for the selection of an appropriate methodological approach aimed to provide an accurate measurement of this highly toxic air pollutant in compliance with the WHO air quality guidelines. Although passive samplers may offer the opportunity to carry out low-cost preliminary surveys, the use of the high-frequency H₂S analyzer is preferred when an accurate assessment of air quality is required. In fact, the latter provides precise real-time measurements for a reliable estimation of the effective exposure to hazardous H₂S concentrations, giving insights into the mechanisms regulating the dispersion of this air pollutant in relation to the meteorological parameters.  相似文献   

云南会泽铅锌矿床分散元素的富集机制——兼论浅色闪锌矿富集Cd的原因          下载免费PDF全文

张茂富  周宗桂  熊索菲  宫勇军  姚书振  李行 《地质找矿论丛》2016,31(1):18-28

文章对云南会泽铅锌矿床的黄铁矿、方铅矿和闪锌矿中的分散元素进行了电子探针分析(EMPA),探讨了分散元素的富集机制.结果表明,分散元素含量已达到综合利用指标,且富集规律为:分散元素以类质同象的形式赋存,黄铁矿中分散元素含量较低,而方铅矿中分散元素的含量稍高于闪锌矿.闪锌矿中:Cd富集顺序为红色＞杂色＞黑色,在高温阶段Cd置换Fe,低温阶段Cd置换Zn;Ga通过置换Zn进入闪锌矿,Ge可能主要替代Fe而进入闪锌矿晶格.方铅矿中:Cd和Ga元素置换Fe或Pb先进入方铅矿晶格内,Ge则富集较晚,具体表现为:当Ga含量较低时,元素进入方铅矿品格顺序为Fe,Zn→Cd→Ga,Ge,当Ga含量较高时,元素进入方铅矿品格的顺序依次为Cd,Ga→Ge.  相似文献   

湘西北寒武系沉积型镍钼矿成矿物质来源   总被引：1，自引：0，他引：1  

闫友谊 《江苏地质》2016,40(4):560-566

湘西北寒武系含矿丰富,在寒武系下统牛蹄塘组黑色岩系中赋存有磷矿、石煤、钒矿、铀矿,并有有色金属钼、镍矿及铂族元素矿物聚集。通过分析总结前人成果资料,探究镍钼矿成矿地质环境条件是在低温环境、有微生物参与及强还原环境中同生沉积,对寒武系沉积型镍钼矿成矿物质来源提出了明确的看法,即成矿物质来源于海底喷流-热水。  相似文献   

金川铜镍矿床中新生代抬升冷却过程：来自裂变径迹的证据     

田向盛  杨婧  刘东晓  第鹏飞 《甘肃地质》2016,25(2):50-55

本文基于热年代学理论,利用锆石和磷灰石裂变径迹测年数据及对磷灰石热史的模拟,分析探讨金川铜镍矿床在中新生代的抬升冷却过程,认为金川超基性岩体自中生代以来一直处于持续的冷却抬升阶段,且在中侏罗世和晚白垩世早期经历了两期快速的抬升冷却事件,推断此事件与青藏高原后期活动时间相对应,证明金川岩体受到该事件的远程效应波及,致使该矿床遭受了一定的改造。  相似文献   

滇东南安那金矿床成矿流体地球化学研究   总被引：1，自引：1，他引：0  

董文斗  沈能平  苏文超  蔡佳丽 《岩石学报》2016,32(11):3321-3330

云南安那金矿床位于右江盆地南缘,产于二叠纪辉绿岩侵入体之中,广泛发育乳白色石英网脉,蚀变辉绿岩体即为金矿体。与右江盆地以沉积岩为容矿岩石的卡林型金矿床类似,具有硅化、粘土化、碳酸盐化和硫化物化等热液蚀变特征。本文对安那金矿床石英中的流体包裹体岩相学、显微测温学、激光拉曼光谱以及氢氧同位素组成进行了分析,发现成矿期石英中的流体包裹体主要为富含CO_2气-液两相或三相流体包裹体,其均一温度范围为208~312℃(平均254℃),盐度很低,变化范围为0~2%Na Cleqv,成矿溶液的密度为0.88~0.98g/cm~3,表明形成安那金矿床的成矿流体属于中温、低盐度、中-低密度的流体。激光拉曼光谱分析显示,石英中包裹体的气相成分富含CO_2、N_2以及微量CH_4等挥发分。成矿流体的氢氧同位素组成显示变质流体成因,结合矿石显微岩相学结构,认为流体溶蚀交代辉绿岩中的含Ti-Fe辉石或者钛铁矿,溶解Fe的硫化作用过程是含Au黄铁矿和毒砂沉淀富集的重要机制。成矿作用可能与右江盆地南缘印支期造山事件有关。  相似文献   

Hydrothermal Fluid Sources of the Fengjia Barite–fluorite Deposit in Southeast Sichuan,China: Evidence from Fluid Inclusions and Hydrogen and Oxygen Isotopes          下载免费PDF全文

Hao Zou  Shou‐ting Zhang  An‐qing Chen  Yi Fang  Zhao‐fa Zeng 《Resource Geology》2016,66(1):24-36

The Fengjia barite–fluorite deposit in southeast Sichuan is a stratabound ore deposit which occurs mainly in Lower Ordovician carbonate rocks. Here we present results from fluid inclusion and oxygen and hydrogen isotope studies to determine the nature and origin of the hydrothermal fluids that generated the deposit. The temperature of the ore‐forming fluid shows a range of 86 to 302 °C. Our detailed microthermometric data show that the temperature during mineralization of the fluorite and barite in the early ore‐forming stage was higher than that during the formation of the calcite in the late ore‐forming stage. The salinity varied substantially from 0.18% to 21.19% NaCl eqv., whereas the density was around 1.00 g/cm³. The fluid composition was mainly H₂O (>91.33%), followed by CO₂, CH₄ and traces of C₂H₆, CO, Ar, and H₂S. The dominant cation was Na⁺ and the dominant anion Cl^‐, followed by Ca²⁺, SO₄^2‐, K⁺, and Mg²⁺, indicating a mid–low‐temperature, mid‐low‐salinity, low‐density NaCl–H₂O system. Our results demonstrate that the temperature decreased during the ore‐forming process and the fluid system changed from a closed reducing environment to an open oxidizing environment. The hydrogen and oxygen isotope data demonstrate that the hydrothermal fluids in the study area had multiple sources, primarily formation water, as well as meteoric water and metamorphic water. Combined with the geological setting and mineralization features we infer that the stratabound barite–fluorite deposits originated from mid–low‐temperature hydrothermal fluids and formed vein filling in the fault zone.  相似文献   

吉林白山刘家堡子狼洞沟金银矿床地球化学特征及成因探讨          下载免费PDF全文

吴明刚  王胜炬  王贤孝 《山东国土资源》2016,32(4):17-21

通过对刘家堡子-狼洞沟金银矿床地质、成矿元素和同位素地球化学特征的分析和研究,发现矿区内近EW向和NE向断裂构造是主要容矿构造;最佳找矿元素前缘晕组合为As-Sb-Zn,矿上晕元素组合为Au-Ag-Pb-Hg,尾晕元素组合为Ni-Cu-Co;成矿作用中,古老基底中元古宙老岭群变质岩系为成矿提供了丰富的物质来源,而燕山期构造岩浆活动在提供成矿物质的同时还提供了热动力。刘家堡子-狼洞沟金银矿床应划属为与燕山晚期超浅成中酸性岩浆岩有关的中低温热液构造裂隙充填型金银矿床。  相似文献   

The source of sulfur in sulfide deposits in the Siberian Platform traps (from isotope data)     

V.V. Ryabov  O.N. Simonov  S.G. Snisar  A.A. Borovikov 《Russian Geology and Geophysics》2018,59(8):945-961

The source of sulfur in giant Norilsk-type sulfide deposits is discussed. A review of the state of the problem and a critical analysis of existing hypotheses are made. The distribution of δ³⁴S in sulfides of ore occurrences and small and large deposits and in normal sedimentary, metamorphogenic, and hypogene sulfates is considered. A large number of new δ³⁴S data for sulfides and sulfates in various deposits, volcanic and terrigenous rocks, coals, graphites, and metasomatites are presented. The main attention is focused on the objects of the Norilsk and Kureika ore districts. The δ³⁴S value varies from -14 to + 22.5‰ in sulfides of rocks and ores and from 15.3 to 33‰ in anhydrites. In sulfide-sulfate intergrowths and assemblages, δ³⁴S is within 4.2-14.6‰ in sulfides and within 15.3-21.3‰ in anhydrites. The most isotopically heavy sulfur was found in pyrrhotite veins in basalts (δ³⁴S = 21.6‰), in sulfate veins cutting dolomites (δ³⁴S = 33‰), and in subsidence caldera sulfates in basalts (δ³⁴S = 23.2-25.2‰). Sulfide ores of the Tsentral’naya Shilki intrusion have a heavy sulfur isotope composition (δ³⁴S = + 17.7‰ (n = 15)). Thermobarogeochemical studies of anhydrites have revealed inclusions of different types with homogenization temperatures ranging from 685 °C to 80 °C. Metamorphogenic and hypogene anhydrites are associated with a carbonaceous substance, and hypogene anhydrites have inclusions of chloride-containing salt melts. We assume that sulfur in the trap sulfide deposits was introduced with sulfates of sedimentary rocks (δ³⁴S = 22-24‰). No assimilation of sulfates by basaltic melt took place. The sedimentary anhydrites were “steamed” by hydrocarbons, which led to sulfate reduction and δ³⁴S fractionation. As a result, isotopically light sulfur accumulated in sulfides and hydrogen sulfide, isotopically heavy sulfur was removed by aqueous calcium sulfate solution, and “residual” metamorphogenic anhydrite acquired a lighter sulfur isotope composition as compared with the sedimentary one. The wide variations in δ³⁴S in sulfides and sulfates are due to changes in the physicochemical parameters of the ore-forming system (first of all, temperature and P_ch4) during the sulfate reduction. The regional hydrocarbon resources were sufficient for large-scale ore formation.  相似文献   

内蒙古兴和县曹四夭超大型斑岩钼铅锌金成矿系统年代学及其地质意义     

范海洋  李铁刚  武文恒  张明玉  黄凡  赵正  张彤  许立权  李香资  权知心 《矿床地质》2018,37(2):355-370

曹四夭斑岩钼矿床位于内蒙古兴和县,是华北克拉通北缘最大的钼矿床。该矿床中部发育斑岩型钼矿体,外围和上部产出热液脉型铅锌金矿体。文章选取1件与斑岩钼矿化共生的绢云母样品进行了40Ar-39Ar定年,获得40Ar-39Ar坪年龄为(144.4±1.2)Ma,相应的39Ar/36Ar-40Ar/39Ar等时线年龄为(146.4±2.2)Ma(MSWD=0.31),将等时线年龄认作绢云母的Ar封闭年龄,表明曹四夭斑岩钼矿化发生在约146 Ma前。选取14件脉型铅锌矿石中的闪锌矿、黄铁矿和磁黄铁矿样品开展了Rb-Sr定年,获得4件闪锌矿的Rb-Sr等时线年龄为(145.1±3.0)Ma(MSWD=0.63);5件黄铁矿的Rb-Sr等时线年龄为(145.2±1.3)Ma(MSWD=0.53);4件闪锌矿、5件黄铁矿和1件磁黄铁矿的Rb-Sr等时线年龄为(145.3±1.0)Ma(MSWD=0.43)。硫化物Rb-Sr定年结果表明曹四夭矿床脉型铅锌矿化形成于约145 Ma前。本次绢云母40Ar-39Ar和硫化物Rb-Sr定年结果表明,曹四夭矿床斑岩型钼矿化和脉型铅锌金矿化为同期产物,两者均形成于晚侏罗世末期,属于同一个斑岩成矿系统。曹四夭矿床硫化物的w(Rb)和w(Sr)分别为0.1867×10~(-6)~1.305×10~(-6)和0.3175×10~(-6)~6.935×10~(-6),Sr同位素初始比值(87Sr/86Sr)i介于0.709 919~0.711 951之间,平均值0.710 952,结合前人获得的辉钼矿Re含量,认为曹四夭矿床的成矿物质主要来源于地壳。  相似文献   

现代海底块状硫化物矿床储量估算方法探讨     

张柏松 《地质与勘探》2018,54(4):723-734

海底块状硫化物矿床具有巨大的经济价值和良好的开发前景。但是由于勘探难度和技术手段的限制,在全球已经发现的600多个海底热液喷口和硫化物矿床中,不到5%的矿床进行了详细的勘探,进行资源量计算的矿床更是屈指可数。选择适当的方法估算储量对于深海资源开发意义重大。本文系统总结了前人估算海底硫化物储量的方法,并以勘探程度相对较高、数据资料相对丰富的Atlantis-II-Deep矿床和Solwara 1矿床为例,评析了前人采用不同储量计算方法得到的结果和各种方法计算的准确性;针对有一定钻孔数据的TAG硫化物堆丘,采用距离反比法重新计算了储量,并和块段法估算的结果进行对比。得到以下结论:(1)海底硫化物矿体形态是制约储量估算方法适用性的一个重要因素;(2)传统几何法可以在极低勘探条件下估算海底硫化物储量量级;(3)对于海底硫化物储量估算,地质统计学的精度高于传统几何法;(4)较高勘探条件下距离反比法可以与地质统计学相互对照、验证;(5)在一定钻孔数量的条件下,可以应用距离反比法进行海底硫化物储量估算。  相似文献