Sulfur Isotope Fractionation in Magmatic Systems：Models of Rayleigh Distillation and Selective Flux   总被引：2，自引：0，他引：2  

郑永飞 《中国地球化学学报》1990,9(1):27-45

The effect of Rayleigh distillation by outgassing of SO2 and H2S on the isotopic composition of sulfur remaining in silicate melts is quantitatively modelled.A threshold mole fraction of sulfur in sulfide component of the melts is reckoned to be of critical importance in shifting the δ^34S of the melts mith respect to the original magmas.The partial equilibrium fractionation in a magmatic system is evaluated by assuming that a non-equilibrium flux of sulfur occurs between magmatic volatiles and the melts,while an equilibrium fractionation is approached between sulfate and sulfide within the melts.The results show that under high fo2 conditions,the sulfate/sulfide ratio in a melt entds to increase,and the δ^34S value of sulfur in a solidified rock might then be shifted in the positive direction.This may either be due to Rayleigh outgassing in case the mole fraction of sulfide is less than the threshold,or due to a unidirectional increase in δ^34S value of the sulfate with decreaing temperature,Conversely,at low fo2,the sulfate/sulfide ratio tends to decrease and the δ^34S value of total sulfur could be driven in the negative direction,either because of the Rayleigh outgassing in case the mole fraction of sulfide is greater than the threshold,or because of a unidirectional decrease inδ^34S value of the sulfide.To establish isotopic equilibrium between sulfate and sulfide,the HM,QFM or WM buffers in the magmatic system are suggested to provide the redox couple that could simultaneously reduce the sulfate and oxidize the sulfide.CaO present in the silicatte Melts is also called upon to participate in the chemical equilibrium between sulfate and sulfide,Consequently,the δ^34S value of an igneous rock could considerably deviate from that of its original magma due to the influence of oxygen fugacity and temperature at the time of magma solidification.  相似文献   

Associations and mobility of uranium in soils near a depleted uranium （DU） weapons testing site, SW Scotland     

Margaret C. Graham John G. Farmer Ian W. Oliver Angus B. MacKenzie Robert M. Ellam 《中国地球化学学报》2006,25(B08):112-112

Natural uranium has three isotopes, ^238U, ^235U and ^234U, with natural abundances of 99.27 atom %, 0.72% and 0.0055%, respectively. Only ^235U is fissile and the production of nuclear fuel and nuclear weapons involves enrichment of uranium in ^235U. This process also results in separation of ^234U from ^238U, leaving depleted uranium （DU）, with typical ^234U/^238U and ^235U/^238U activity ratios of about 0.19 and 0.013, respectively, as a waste product. The high density, high melting and boiling points and chemical stability of uranium and the availability of DU in relatively pure form mean that DU has many uses, including armour-piercing munitions. Such munitions have been developed in the UK since the 1960s and testing has been carried out by the Ministry of Defence （MoD） at firing ranges such as Dundrennan, SW Scotland and Eskmeals, NW England. The firing of DU munitions can result in the dispersion of DU and its combustion products （oxides） as aerosols or as larger fragments, with the potential for human exposure either directly at the site of detonation or via post-depositional migration in the environment. The aim of this work was to investigate the potential environmental mobility of DU by characterizing the associations of U in soil porewaters with increasing distance from a firing site. To this end, several soil cores located down-wind of the firing site at Dundrennan, near Kirkcudbright, SW Scotland, were collected in May 2006. These were sectioned on-site into 1- or 2-cm depth intervals and porewaters were isolated by centfifugation （10 minutes; 8873 g） on return to the laboratory. Following filtration through 0.2-micron cellulose nitrate filters, the porewaters were analyzed by ICP-QMS （U concentration） and ICP-OES （Fe, Al, Ca, Mg, Mn concentrations）. Sub-samples were also subjected to centrifugal ultrafiltration （100, 30, and 3 kD） and to gel electrophoretic fractionation （agarose; 0.045 M Tris-borate; 20 mA, 30 minutes）. Results showed that U was present at up to 4 μg/L in the soil porewater and that the associations of U varied with sample location and soil depth.  相似文献   

Possibility of degradation of phenylarsonic acid in the presence of ferrihydrite     

Yoko Shimamoto Yoshio Takahashi 《中国地球化学学报》2006,25(B08):114-114

Although inorganic species are predominant in natural systems, but there are many kinds of organoarsenic species such as methylated and phenylated arsenic compounds. Phenylarsonic acid （PA） is a degradation product of organoarsenics used for chemical warfare agents, which has been detected in well water at the disposal site of the agents in Japan. There are few reports studying behavior of PA in soil. In this study, PA was adsorbed onto ferrihydrite and its chemical forms were determined using high performance liquid chromatography connected to inductivity-coupled plasma mass spectrometry （HPLC-ICP-MS）. 100 mg/kg of PA was mixed with 0.03 g of 2-line ferrihydrite. For each suspension, pH was adjusted by HNO3 or NaOH. Each sample was incubated for more than 19 hours and the final pH was measured. After filtration, the chemical form of arsenic in the filtrate was measured using HPLC-ICP-MS. In addition, ferrihydrite separated by filtration was dissolved by 3 ml of 0.5 M HCI and the arsenic species in the solution was detected by HPLC-ICP-MS （column： Tosoh TSKgel SuperlC-AP, eluent： 0.01 M HNO3）. It was verified that PA is not degraded by heating in 0.5 M HCl solution. At pH 3.1, any arsenic compounds were not detected from the solution, because almost all arsenic species were adsorbed onto ferrihydrite at lower pH. At pH= 12, however, 7%-10% of inorganic arsenic was detected in the solution. In solid phase, there are some problems to determine the precise ratio of inorganic and organic species. When the solution includes Fe ion at 0.01 M level, the retention time of arsenic species drifted compared to those in standard solution, which makes it difficult to determine precisely the arsenic species adsorbed on ferrihydrite. Therefore, more study is needed to determine the ratio of inorganic and organic species in the system.  相似文献   

Assessment of marine pollution in Daya Bay, South China： Nutrients, heavy metals and persistent organic pollutants     

《中国地球化学学报》2006,25(B08):166-166

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DDT residue in soil and water in and around the abounded area of DDT manufacturing factory     

Mohammad Rasul Jan Mahmood A Khawaja Jasmin Sha Kashif Gul 《中国地球化学学报》2006,25(B08):182-182

Due to the persistent nature of DDT, a persistent organic pollutant and its adverse environmental and health impacts, the present study was undertaken to examine the residual DDT in and around DDT manufacturing factory in Amman Gharh, Nowshera, NWFP. The factory was established in 1963 and remained in operation till 1994. Composite samples of soil, sediments and water were collected in and around the factory area, nearby DDT stores, main factory drain leading to river and nearby villages. Standard procedures were used for the collection, transportation and storage of samples for analysis. Physical parameters for the collected water samples measured were temperature, pH and conductance. Extraction of each sample for DDT analyses was carried out in triplicates using soxhlet extraction apparatus. The extract was transferred to well washed, clean; dry glass vial, sealed and put in the refrigerator. Gas Chromatograph with electron capture detector and capillary column was used for analysis. DDT in the samples was identified on the basis of their retention time and quantified on the basis of peak areas. It is evident from the analytical data obtained in the present study that both water and soil in and around the factory area are still contaminated with DDT, despite the closure of the factory since the past few years.  相似文献   

Occurrence of microorganic pollutants in the atmosphere of Singapore during haze and non-haze periods     

Rajasekhar Balasubramanian Chanbasha Basheer Kang Lisa Siao Wei See 《中国地球化学学报》2006,25(B08):183-183

Microorganic pollutants such as polycylic aromatic hydrocarbons （PAHs）, organochlorine pesticides （OCPs）, polychlorinated biphenyls （PCBs） and total petroleum hydrocarbons （TPHs） are known to be present in urban ambient air. These organic compounds are prone to atmospheric transport and deposition over long distances, thus enabling them to accumulate even in regions remote from their sources. Deposition from the atmosphere can be via direct deposition and exchange with crops that may be directly or indirectly ingested by humans. It can also take place via wet and dry deposition and air-water exchange. Following their deposition, these microorganic pollutants tend to accumulate in soils, sediments and in human and ecological food chains. There are many reports in the literature on the atmospheric concentrations of microorganic pollutants, but there are few reports and data in Asia. This study was performed in Singapore to determine the relative amounts of persistent organic pollutants and TPHs in ambient aerosols. One of the important sources of these organic compounds in Southeast Asia is thought to be biomass burning （vegetation fires）. Hence, air sampling was conducted during both smoke haze and non-haze periods. The data obtained from this study will be presented and discussed.  相似文献   

Water chemical behavior at Yangtze （Changjiang） River estuary     

Sivaji Patra Congqiang LIU Siliang LI Fushun WANG Baoli WANG 《中国地球化学学报》2006,25(B08):269-270

Geochemical cycling has received wide attention due to the need to understand the pathways of pollutants through our present environment. In this regard the Yangtze River plays a significant role in putting those pollutants into the East China SeafWorld Oceans. The Yangtze River is of high sedimentation rate and water discharge. The watershed covers variable climate regions from temperate to subtropical and from semiarid to humid. Twenty three （23） sampling locations at the estuary have been selected for understanding the dynamic relationships. The elements （Cl^-, SO4^2-, Na^＋, K^＋, and Ca^2＋） show conservative behavior during mixing of fresh water with saline water whereas Mg^2＋, Mn^2＋ show a non-conservative pattern . The relationships between Na^＋/SO4^2- and Cl^-/SO4^2- molar ratios show a mixing of more than two water sources.  相似文献   

紫色丘陵区不同土地利用方式下土壤活性有机碳垂直分布特征     

《山地学报》2006,24(B10):21-26

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马朗凹陷马1井储层长石中有机包裹体研究          下载免费PDF全文

张小青  伊海生  危国亮  张小芹 《沉积与特提斯地质》2005,25(4):83-86

根据对马朗凹陷马1井储层长石中有机包裹体的基本特征、均一温度、荧光及荧光光谱分析，得出有机包裹体均一温度为60～90℃．120～140℃，其对应的荧光颜色分别为黄色和蓝绿色。认为储层的油气运移经历了两期，第一期为烃类的主要运移、聚集期，油气为低成熟油；第二期为少量的烃类聚集，并判断出二叠系条湖组该段储层为油气产层。  相似文献   

江西彭山锡多金属矿田地质地球化学特征研究   总被引：1，自引：0，他引：1       下载免费PDF全文

卢树东高文亮  汪石林肖 锷 许建华 《中国地质》2005,32(3):463-469

彭山锡多金属矿田位于长江中下游的九瑞地区，是近年来发现的一个以富锡、铅、锌矿产为主的大型矿田。以黑云母二长花岗岩与二云母碱长化岗岩组成的彭山隐伏岩体为中心，各类金属矿床呈“晕圈式”分布。矿床的形成分为2个成矿期共7个阶段，通过对彭山岩体、典型矿床及围岩中的硫同位素、铅同位素、包裹体及稀土资料进行分析，反映出燕山晚期钙碱性花岗岩体的缦位与多金属矿床的形成有着密切的联系，岩浆活动为本区提供了大量的成矿物质。  相似文献