Hydroperoxides in the marine troposphere over the Atlantic Ocean     

F. Slemr  H. G. Tremmel 《Journal of Atmospheric Chemistry》1994,19(4):371-404

Hydrogen peroxide (H₂O₂) and organic hydroperoxides (ROOH) were measured on board of theRV Polarstern during its cruise across the Atlantic Ocean from 20 October to 12 November 1990 (54° N to 51° S latitude) by the enzyme fluorometric method. The H₂O₂ mixing ratio varied from below the detection limit of about 0.12 ppbv up to 3.89 ppbv, showing a latitudinal dependence with generally higher values around the equator and decreasing values poleward. The shape of the latitudinal H₂O₂ distribution agrees well with an analytical steady state expression for H₂O₂ using the measured H₂O and O₃ distribution and a wind dependent H₂O₂ deposition rate. The ROOH mixing ratio varied from below the detection limit of about 0.08 ppbv up to 1.25 ppbv with qualitatively the same latitudinal dependence as H₂O₂. The observed ratio ROOH/(ROOH + H₂O₂) varied between 0.17 and 0.98 showing higher values at the lowest H₂O₂ mixing ratios at high latitudes. The measured H₂O₂ mixing ratio shows a significant diurnal variation with a maximum around 14:00 local time, explicable by a superposition of the photochemical H₂O₂ production with a constant H₂O₂ deposition rate. Four independent estimations of the average effective H₂O₂ deposition rate inferred from the H₂O₂ decrease in the night, from the midday H₂O₂ production deficit (as derived from comparison with a photochemical model and from the daily ozone loss), and from the offset in the latitudinal H₂O₂ distribution, were consistent. An episode of maximum H₂O₂ concentration suggests the possibility of its formation in clouds.  相似文献   

Mineral-chemistry and stable-isotope constraints on the magmatism, hydrothermal alteration, and related PGE–(base-metal sulphide) mineralisation of the Mesoarchaean Baula-Nuasahi Complex, India     

Thierry Augé  Catherine Lerouge 《Mineralium Deposita》2004,39(5-6):583-607

The Baula-Nuasahi Complex, on the southern flank of the Singhbhum Archaean nucleus in north-eastern India, exposes a series of Mesoarchaean igneous suites. These are (1) a gabbro–anorthosite unit, which is petrographically homogeneous, although mineral-chemistry data hint at a subtle eastward differentiation; (2) a peridotite unit (with three chromitite layers) together with (3) a pyroxenite unit which display cumulate textures, modal layering, and (for the peridotite unit) differentiation trends in both mineralogy and mineral chemistry; and (4) the Bangur gabbro (~3.1 Ga), which defines an oblong intrusion, crosscutting the older igneous suites in the southern part of the complex, with a curvilinear NW-trending apophysis, 2 km long and up to 40 m wide. Magmatic breccia comprising ultramafic and chromitite wall-rock clasts in a gabbro matrix is exposed at the contact of the main Bangur gabbro body and also forms the entire Bangur gabbro apophysis. Concentrations of platinum-group minerals (PGMs) are found where the breccia contains abundant chromitite clasts, and two types of platinum-group-element (PGE) mineralisation are recognised. Type 1 (Pt 1.1–14.2, Pd 0.1–2.1 ppm, with an average Pt/Pd=8–9) is a contact-type mineralisation which occurs in the breccia at the contact between the Bangur intrusion and its ultramafic host. The PGMs—Pt alloys (isoferroplatinum) and sulphides (braggite, malanite)—are enclosed by pyroxene and plagioclase, reflecting a magmatic origin. Significant wall-rock assimilation by the magma (giving rise to the Bangur gabbro) is indicated by changes in pyroxene composition and by the presence of relicts of chromite (from the host) now altered to secondary ferritchromite in the contact zone. Type 2 PGE mineralisation (Pt 0.3–1.6, Pd 1.8–6.0 ppm, with Pt/Pd~0.5–3.0) is restricted to the breccia apophysis of the Bangur gabbro where it occurs in the breccia matrix, associated with an intense hydrothermal alteration which does not exist in the contact zone. PGMs (PGE arsenides, tellurides, bismuthides and antimonides) and, where present, base-metal sulphides (BMSs) form intergrowths with hydrous silicates, reflecting a hydrothermal origin. Oxygen isotope geothermometry documents the main stages of hydrothermal alteration within a decreasing temperature range between 700–1,000 and 500–600 °C, and oxygen, hydrogen and sulphur isotopes show that the hydrothermal fluids were derived from the magma rather than an external source. Pervasive hydrothermal alteration in the breccia apophysis likely represents upward channelling of late-magmatic fluids along a narrow, near-vertical, subplanar conduit which led away from the main magma chamber. We suggest that Type 2 mineralisation was produced by late-magmatic hydrothermal remobilisation and reconcentration of Type 1 PGE mineralisation, and that the composition of the hydrothermal fluids controlled whether BMSs were enriched along with the PGMs.Editorial handling: P. Lightfoot  相似文献   

四川大渡河金矿田成矿流体来源的氦氩硫氢氧同位素示踪   总被引：12，自引：3，他引：12       下载免费PDF全文

李晓峰毛景文  王登红罗辅勋 《地质学报》2004,78(2):203-210

四川大渡河金矿田位于扬子地台西缘金成矿带北段,受大渡河剪切带控制。本文以该矿田黄金坪、白金台子、黑金台子金矿为例,根据对黄铁矿流体包裹体氦氩同位素、黄铁矿硫同位素以及与黄铁矿共生的石英流体包裹体的氢氧同位素组成测定,讨论了大渡河金矿田成矿流体的来源。结果显示,该金矿田黄铁矿流体包裹体中的~3He/~4He变化较小,为0.16～0.86Ra,而~(40)Ar/~(36)Ar的变化较大,为298～3288;而黄铁矿δ~(34)S同位素变化范围较窄,一般为0.7‰～4.2‰,集中于2.5‰～3‰,显示硫地幔来源的特点;石英流体包裹体的氢、氧同位素分别为-2.6‰～ 3.64‰和-39.13‰～-108.23‰,说明成矿流体为岩浆水和大气降水的混合流体。本文认为大渡河金矿田成矿流体是地幔流体与地壳流体的混合作用的结果,而以地壳流体占主导地位。其中,地幔流体为与下伏隐伏岩体有关的岩浆水,而地壳流体端元则是含有一定放射成因Ar的大气降水,并且温度小于200℃。  相似文献   

Hydrogen isotopic compositions, distributions and source signals of individual n-alkanes for some typical crude oils in Lunnan Oilfield, Tarim Basin, NW China     

LU Hong  LI Chao  SUN Yongge  PENG Ping’an & XIAO Zhongyao . State Key Laboratory of Organic Geochemistry  Guangzhou Institute of Geochemistry  Chinese Academy of Sciences  Guangzhou  China  . Tarim Research Institute of Exploration  Development of Petroleum  China Petroleum  Korla  China 《中国科学D辑(英文版)》2005,48(8):1220-1226

Petroleum mainly comprises carbon and hydrogen elements. The stable carbon isotopic analysis for whole oil was undertaken as early as the 1930s. After decades, the stable carbon isotopic analytical methods have been developed from analysis for whole oil and oil fractions (e.g., saturated, aromatic and polar frac-tions) into compound-specific isotopic analysis with the emergence of the newly developed GC-C-IRMS analytical technique. Especially, by using com-pound-specific isotopic analytical…  相似文献   

凡口铅锌矿床同位素地球化学证据   总被引：3，自引：0，他引：3  

汪礼明  徐文忻  李蘅  彭省临 《地球学报》2005,26(Z1):164-167

对凡口铅锌矿床不同成矿阶段进行矿物包裹体温度、硫和铅同位素测定，获得成矿第Ⅰ阶段温度为300±50℃，第Ⅱ、Ⅲ阶段温度为250±50℃；并获得矿床硫化物的S同位素组成为2.1‰～26.5‰，具有δ34SPy＞δ34SSp＞δ34SGn；第Ⅰ阶段硫化物的硫同位素组成随赋存层位由老到新硫同位素有逐渐减小趋势；第Ⅱ阶段硫化物的δ34S为14.3‰～23.8‰；第Ⅲ阶段硫化物的δ34S为5.7％~15.7‰，具有从早阶段至晚阶段硫同位素组成变化范围从大至小的减小趋势。分析获得68件铅同位素数据，其中硫化物的206Pb/204Pb比值为18.023～18.847；207Pb/204Pb比值为15.700～15.820；208Pb/204Pb比值为38.056～39.796。灰岩全岩的206Pb/204Pb比值为18.230～18.860；207Pb/204Pb比值为15.640～16.000；208Pb/204Pb比值为38.714～39.960。辉绿岩的206Pb/204Pb比值为18.570～18.650；207Pb/204Pb比值为15.260～15.620；208Pb/204Pb比值为38.650～38.960。第Ⅰ阶段δ34OH2O为13.3‰~13.1‰，δD为－50.2‰～－61.5‰；第Ⅱ阶段δ18OH2O为－2.4‰～＋10.8‰，δD为－50.2‰～－63.2‰；第Ⅲ阶段δ18OH2O为－4.9‰～－14.3‰，δD为－59.0‰～－61.0‰。  相似文献   

Geological and Geochemical Characteristics of the Zhulazhaga Gold Deposit in Inner Mongolia, China     

JIANG Sihong  NIE Fengjun Institute of Mineral Resources  Chinese Academy of Geological Sciences  Beijing 《《地质学报》英文版》2005,79(1):87-97

Located in Alxa Zuoqi (Left Banner) of Inner Mongolia, China, the Zhulazhaga gold deposit is the first largescale gold deposit that was found in the middle-upper Proterozoic strata along the north margin of the North China craton in recent years. It was discovered by the No. l Geophysical and Geochemical Exploration Party of Inner Mongolia as a result of prospecting a geochemical anomaly. By now, over 50 tonnes of gold has been defined, with an average Au grade of 4 g/t. The ore bodies occur in the first lithological unit of the Mesoproterozoic Zhulazhagamaodao Formation (MZF), which is composed mainly of epimetamorphic sandstone and siltstone and partly of volcanic rocks. With high concentration of gold,the first lithological unit of the MZF became the source bed for the late-stage ore formation. Controlled by the interstratal fracture zones, the ore bodies mostly appear along the bedding with occurrence similar to that of the strata. The primitiveore types are predominantly the altered rock type with minor ore belonging to the quartz veins type. There are also some oxidized ore near the surface. The metallic minerals are composed mainly of pyrite, pyrrhotite and arsenopyrite with minor chalcopyrite, galena and limonite. Most gold minerals appear as native gold and electrum. Hydrothermal alterations associated with the ore formation are actinolitization, silicatization, sulfidation and carbonation. A total of 100 two-phase H2O-rich and 7 three-phase daughter crystal-beating inclusions were measured in seven goldbearing quartz samples from the Zhulazhaga gold deposit. The homogenization temperatures of the two-phase H2O-rich inclusions range from 155 to 401℃, with an average temperature of 284℃ and bimodal distributions from 240 to 260℃ and 300 to 320℃ respectively. The salinities of the two-phase H2O-rich inclusions vary from 9.22wt% to 24.30wt% NaCl eqniv, with a mode between 23 wt% and 24wt% NaC1 equiv. Comparatively, the homogenization temperatures of the threephase daughter crystal-beating inclusions vary from 210 to 435℃ and the salinities from 29.13wt% to 32.62wt% NaCl equiv. It indicates that the ore-forming fluid is meso-hypothermal and characterized by high salinity, which is apparently different from the metamorphic origin with low salinity. It suggests a magmatic origin of the gold-bearing fluid. The δ^18O values of quartz from auriferous veins range from 11.9 to 16.3 per mil, and the calculated δ^18OH2O values in equilibrium with quartz vary from 1.06 to 9.60 per mil, which fall between the values of meteoric water and magmatic water. It reflects that the ore-forming fluid may be the product of mixing of meteoric water and magmatic water.Based on geological and geochemical studies of the Zhulazhaga gold deposit, it is supposed that the volcanism in the Mesoproterozoic might make gold pre-concentrate in the strata. The extensive and intensive Hercynian tectono-magmatic activity not only brought along a large number of ore-forming materials, but also made the gold from the strata rework. It can be concluded that the ore bodies were mainly formed in late hydrothermal reworking stage. Compared with typical gold deposits associated with epimetamorphic clastic rocks, the Zhulazhaga deposit has similar features in occurrence of ore bodies, ore-controlling structure, wall-rock alterations and mineral assemblages. Therefore, the Zhulazhaga gold deposit belongs to the epimetamorphic clastic rock type.  相似文献   

Degradation of petroleum contaminants in oil     

Yanying SUN Fei LIU Honghan CHEN Wei HE 《中国地球化学学报》2006,25(B08):126-127

The treatment of diesel-contaminated soil with hydrogen peroxide oxidation is investigated in this paper. The factors influencing reactions such as initial oil content, H2O2 dosage, pH-value, catalyst and so on are studied. The results indicate that it is feasible to remediate diesel-contaminated soil by adding oxidant directly at room temperature because of higher absolute removal content although the degradation efficiency is low for the contaminated soil of 1%, 2% and 5% initial oil content. The more the H2O2 dosage, the better the degradation efficiency; it is economical and efficient to add 4 mL H2O2 to 10 g diesel-contaminated soil （2% or so） directly in-situ chemical oxidation （ICO）. For the contaminated soil of 5% initial oil content, when pH-value is 5-8 and H202 dosage is 20 mL, the removal efficiency reaches more than 96%; when pH-value is 1-3 and volume ratios of H2O2 to Fe^2＋ are 1 ： 1, 2：2, the degradation efficiencies are all very high （i.e., 86%-88% or so）. It can be concluded that the degradation efficiencies are comparative when adding 1 mL or 2 mL H2O2 of Fenton Reagent or adding 4 mL of H2O2 only to 10 g diesel-contaminated soil.  相似文献   

加氢和TSR反应对天然气同位素组成的影响   总被引：2，自引：1，他引：2  

刘文汇  张殿伟王晓锋 《岩石学报》2006,22(8):2237-2242

天然气形成过程中的加氢作用和 TSR 反应是有机-无机相互作用的重要方式。相邻水体和深部来源的氢,是天然气形成的重要氢源,塔里木盆地天然气的甲烷氢同位素组成明显表现出不同沉积水体对甲烷氢同位素的控制作用,大宛105～25井和阿克1井具有深部流体加氢的特征;TSR 反应中硫同位素在不同反应阶段和反应过程具有不同的分馏特征,这种特征在四川盆地高舍硫天然气中具有很好的表现,TSR 反应硫同位素分馏一般小于20‰,而单体硫、黄铁矿和硫酸盐矿物等其它反应过程的产物硫同位素分馏不明显。  相似文献   

Hydrogen Isotope Study of Fluid Inclusions in Vein Quartz of the Hishikari Gold Deposits, Japan   总被引：1，自引：0，他引：1  

Akira IMAI  Hidehiko SHIMAZAKI  Tomoko NISHIZAWA 《Resource Geology》1998,48(3):159-170

Abstract: The origin of mineralizing fluids responsible for the Hishikari vein-type epithermal Au deposits was studied on the basis of the hydrogen isotopic ratio (δD) of the inclusion fluid from vein quartz and adularia. The origin of hydrothermal fluids was estimated by combination of the present δ values and the oxygen isotopic ratios (δ¹⁸O) previously reported by Shikazono and Nagayama (1993). The water in the fluid inclusions was extracted by means of decrepitation of quartz at 500°C. Hydrogen was obtained by reduction of the collected water with Zn shot at 450°C. The δD values were determined by mass spectrometer. The δD values of inclusion fluid obtained from quartz range from –61 to –114%. These are significantly lower than the δD value of the thermal water presently venting from the Hishikari deposits and that of local meteoric water. Hydrogen isotopic fractionation between water and amorphous silica, which might have initially precipitated from the hydrothermal fluids at least partly, is not a probable cause of this isotopic depletion, while some water might have been released from the initial hydrous amorphous silica during recrystallization to quartz observed presently. Thus, a part of ore fluids for the Hishikari deposits is supposed to have been originated from the water having anomalous δD values of lower than –100%. Such D depletion cannot be caused by simple oxygen-shift of meteoric water or by contribution of magmatic volatiles. The δD values of water released from the shale samples of the Shimanto–Supergroup, a major host to the Hishikari veins range from –132 to –148%. Therefore, the anomalous δD values of inclusion fluids from some vein quartz and adularia suggest that the water released from hydrous minerals of the sedimentary basement rocks by dehydration or the groundwater isotopically exchanged with sedimentary rocks at elevated temperatures during circulation, partly contributed to the hydrothermal fluids responsible for the Hishikari deposits.  相似文献   

橄榄石热解氢释放过程的分析   总被引：14，自引：0，他引：14  

李立武  张铭杰 《地球化学》1998,27(5):514-516

采用分步法热法分析了不同粒度的橄榄石的Ｈ２的质量体系,实验表明,不同粒度的橄榄石释放出的Ｈ２的质量体积不同,随着温度或粒度的变化,Ｈ２的质量体积呈现出规律性的变化,进一步探讨了氢在橄榄石中的赋存状态。  相似文献