胶西北新城金矿床硫同位素地球化学

新城金矿床是胶西北金矿集区中典型的破碎带蚀变岩型金矿床,其热液成矿作用可划分为四个阶段:黄铁矿-石英-绢云母阶段(I)、石英-黄铁矿阶段(II)、石英-多金属硫化物阶段(III)和石英-方解石阶段(IV),其中金主要赋存于II和III阶段的黄铁矿内。该矿床赋矿围岩为郭家岭岩体,岩性为石英二长岩和二长花岗岩,主要为胶东群变质基底经部分熔融形成。胶东群变粒岩硫同位素较为均一(δ34S值介于6.9‰~9.4‰,均值为8.0‰);郭家岭岩体的δ34S值介于6.0‰~16.0‰,均值为8.6‰,反映了其硫同位素组成总体上继承了变粒岩的硫同位素特征;长英质脉岩的δ34S值变化范围为0.8‰~8.5‰(均值为6.7‰),其中4件样品的δ34S值变化范围为7.4‰~8.5‰,反映了其硫主要源自于郭家岭岩体,变粒岩可能提供了部分硫源;而其中1件样品的δ34S值仅为0.8‰,符合岩浆硫来源特征,表明深部岩浆可能也提供了部分硫源。新城金矿床矿石中硫化物δ34S值变化范围较大(4.3‰~10.6‰,均值为8.3‰),表明矿石硫可能源于郭家岭岩体、变粒岩和长英质脉岩,最终主要来源于胶东群变质基底。I阶段黄铁矿颗粒较小(5~600μm),晶形主要为立方体,反映其处于温度较高(300~350℃)、成矿流体的过饱和度较低、低氧逸度和硫逸度、冷却快速、物质供应不足的成矿环境;黄铁矿δ34S值变化范围为8.4‰~10.6‰,均值为9.7‰,反映了矿石硫可能源自于δ34S值较高的郭家岭岩体和变粒岩。II和III阶段黄铁矿粒径变化较大(3μm~2.5mm),晶形主要为五角十二面体,反映其处于中-低温度(200~300℃)、成矿流体过饱和度高、高氧逸度和硫逸度、缓慢冷却同时物质供应充分的成矿环境。其中,II阶段黄铁矿δ34S值变化范围为7.7‰~9.7‰,均值为8.7‰,表明矿石硫源除郭家岭岩体和变粒岩外,δ34S值较低的长英质脉岩可能也提供了部分硫源。III阶段硫化物δ34S值变化范围较大(4.3‰~9.4‰,均值为7.1‰),闪锌矿-方铅矿硫同位素热力学平衡温度范围为180~282℃,氧逸度约为10-37.3~10-36.8,反映了矿石硫源自于郭家岭岩体、变粒岩和长英质脉岩,硫化物δ34S值变化范围较大可能是硫同位素分馏达到平衡的结果。IV阶段黄铁矿粒径最小(1~5μm),为晶形完好、表面光滑的立方体晶形,表明其处于较低温度(200℃),成矿流体的过饱和度较低、氧逸度和硫逸度较低、物质供应不足的成矿环境。     

RESPONSES OF A GLOBAL CGCM TO CO_2 INCREASE

The responses of the climate system to increase of atmospheric carbon dioxide(CO_2)arestudied by using a new version of the Bureau of Meteorological Research Centre(BMRC)globalcoupled general circulation model(CGCM).Two simulations are run:one with atmospheric CO_2concentration held constant at 330 ppm,the other with a tripling of atmospheric CO_2(990 ppm).Results from the 41-year control coupled integration are applied to analyze the mean state,seasonal cycle and interannual variability in the model.Comparisons between the greenhouseexperiment and the control experiment then provide estimations of the influence of increased CO_2on climate changes and climate variability.Especially discussed is the question on whether theclimate changes concerned with CO_2 inerease will impact interannual variability in tropical Pacific,such as ENSO.     

A preliminary study of carbon system in the East China Sea

In the central part of the East China Sea, the activity of CO₂ in the surface water and total carbonate, pH and alkalinity in the water column were determined in winter and autumn of 1993. The activity of CO₂ in the continental shelf water was about 50 ppm lower than that of surface air. This decrease corresponds to the absorption of about 40 gC/m²/yr of atmospheric CO₂ in the coastal zone or 1 GtC/yr in the global continental shelf, if this rate is applicable to entire coastal seas. The normalized total carbonate contents were higher in the water near the coast and near the bottom. This increase toward the bottom may be due to the organic matter deposited on the bottom. This conclusion is supported by the distribution of pH. The normalized alkalinity distribution also showed higher values in the near-coast water, but in the surface water, indicating the supply of bicarbonate from river water. The residence time of the East China Sea water, including the Yellow Sea water, has been calculated to be about 0.8 yr from the excess alkalinity and the alkalinity input. Using this residence time and the excess carbonate, we can estimate that the amount of dissolved carbonate transported from the coastal zone to the oceanic basin is about 70 gC/m²/yr or 2 GtC/yr/area-of-global-continental-shelf. This also means that the rivers transport carbon to the oceans at a rate of 30 gC/m²/yr of the coastal sea or 0.8 GtC/yr/ area-of-global shelf, the carbon consisting of dissolved inorganic carbonate and terrestrial organic carbon decomposed on the continental shelf.     

俯冲带硫的地球化学行为及硫循环SCIEI北大核心CSCD

俯冲带是全球最大的物质循环系统,控制着硫(S)在地球内部圈层及表层的循环,影响着大气圈、水圈、生物圈、岩石圈的稳定性以及地球的宜居性。厘清S在俯冲带中的地球化学行为和循环特征对理解地球各储库的氧化还原状态、岩浆作用与演化、成矿物质聚集、以及地球大气成分等具有重要意义。本文首先总结了进入俯冲带之前的大洋岩石圈的S结构模型,对S在大洋板片中的分布状态和地球化学特征进行了系统归纳。随后,系统阐述了俯冲带高压-超高压变质岩记录的板片变质及脱水过程中硫的地球化学行为。岩石学研究表明俯冲板片中的S多以硫化物相存在,硫酸盐矿物在弧前深度就已被释放或分解。相较于熔体,俯冲带流体中S的溶解度更高,是运移硫的更有效方式。DEW模型计算结果显示,流体中S含量总体较低,但在俯冲板片~90km处其含量有一个峰值(浓度0.5%~1.0%)。岩相学证据、地球化学测试结果、磷灰石S近边吸收结构(S-XANES)特征以及模拟结果都显示俯冲深部流体中S多以HS^(-)及H_(2)S形式存在,不含大量的SO_(4)^(2-)及硫酸盐;中f_(S_(2))流体有利于S迁移出俯冲板片,从而促进俯冲带大规模S循环,而高f_(S_(2))流体在流-岩交换过程沿流体通道发生S的锁固作用而不利于俯冲带S循环。质量平衡计算显示全球俯冲带S输入通量为4.65×10^(13)g/yr,弧下深度板片S输出通量为2.91×10^(12)g/yr,板片-岛弧S循环效率仅6.3%。俯冲板片在弧下深度可能存在一个短暂高效的S释放窗口,释放流体的δ^(34)S值为-2.1±3.0‰。基于高压-超高压变质岩中硫化物的研究,初步厘清了俯冲板片中S的地球化学行为,首次从板片角度全面、定量地限定了俯冲带的脱硫通量、效率、种型和同位素特征,提出俯冲带循环的S不是岛弧岩浆的氧化剂,与岛弧环境的正δ^(34)S值也无直接因果联系,对解析俯冲带S循环和理解地球长期的S循环具有重要意义。最后,本文还展望了俯冲带S循环的未来发展方向,应在俯冲带流体氧化还原性质(硫酸盐的命运)、俯冲沉积物对S循环的制约、俯冲带环境下多硫同位素的分馏效应、S循环与其它挥发分(如C等)循环之间的耦合关系、地球历史上深部S循环等方向做出探索,更深入地理解俯冲带及全球S循环过程。     

碳糊电极循环伏安法测定γ－和β－二氧化锰物相

利用碳糊电极循环伏安法对γ－ＭｎＯ＿２和β－ＭｎＯ＿２进行了定量分析，相对于２００．０ｍｇ碳粉的线性范围分别为γ－ＭｎＯ＿２９．１３～４５，６ｍｇ；β－ＭｎＯ＿２４．５６～３６．５ｍｇ，在线性范围内测量７次，其ＲＳＤ分别为０．５９％～５．２８％和Ｏ％～５．７２％。同时对γ－ＭｎＯ＿２和β－ＭｎＯ＿２的混合试样及湘潭电解二氧化锰也进行了定量测定，其平均相对误差分别为２．０１％～１２．４％和１．９６％～７．５２％。该方法进行物相分析，具有简便、快速、灵敏、经济和不经化学分离等特点。     

中国东部橄榄岩包体和榴辉岩中CO_2流体包裹体的碳同位素组成

应用阶段加热技术 ,对中国东部新生代玄武岩中的橄榄岩包体和大别造山带超高压榴辉岩进行了包裹体 CO2 的碳同位素组成测定。结果表明 ,橄榄岩的δ1 3C值变化较大 ,从 - 2 2 .8‰到 0 .7‰ ,明显不同于前人报道的低δ1 3C值 (- 2 8‰～- 2 0‰ )特征 ,指示中国东部地幔流体中 CO2 的碳同位素组成是不均一的 ,反映了地壳有机碳与原生地幔碳的混合特征。大别造山带榴辉岩的 δ1 3C变化从 - 18.5‰到 4 .6‰ ,同样明显不同于前人报道的低 δ1 3C值 (- 30‰～ - 2 0‰ )特征。榴辉岩的低δ1 3C值指示了板块俯冲前其玄武岩原岩受到地表含有机碳流体蚀变后的碳同位素特点 ,而较高的δ1 3C值反映了板块折返过程中榴辉岩受淋滤大理岩的富 CO2 流体叠加的退变质效应。橄榄岩包体和超高压榴辉岩的轻碳同位素共同特点反映了板块俯冲引起的壳—幔物质相互作用和碳同位素地球化学再循环 ,指示中国东部岩石圈地幔含有丰富的地壳有机碳组分     

苏北盆地油田封存二氧化碳潜力初探

油田二氧化碳封存是减少温室气体排放量最有效的途径之一,油藏中封存CO2 主要有构造地层储存、束缚气储存、 溶解储存和矿化储存等四种方式,CO2 在油藏中的地质储存容量采用国际上通用的资源储量金字塔理论来进行潜力评价。 本文通过分析油田CO2 封存机理,结合江苏省苏北盆地的地质和构造条件,对苏北盆地油田进行CO2 封存潜力研究。苏北 盆地油田多为低渗透和含水油藏,在储存CO2 的潜力上,东台坳陷优于盐阜坳陷,次级单元中又以高邮凹陷、金湖凹陷封 存CO2 潜力最大,一系列小型构造单元比较适合于CO2 封存,并有利于后期的保存。在封盖能力上,苏北盆地在垂向上有 明显的两分性,下部上白垩系和古新统盖层相对上部始新统盖层对CO2 封盖性更好。估算得到苏北盆地油田埋存CO2 的理 论储存容量为1.5054×108 t,有效储存容量为0.0828×108 t~0.4421×108 t,表明苏北油田封存CO2 的潜力较大。     

1994-2006年长江三角洲和东北平原酸性气体浓度变化

 利用长江三角洲和东北平原地区大气本底站的二氧化硫（SO2）和氮氧化物（NOx）历史资料和近期取得的观测数据,探讨两个地区人为排放对这些气候相关酸性气体的不同贡献。从两种酸性气体过去和现在的浓度水平,估算了它们在两个地区的增长率,比较了NOx与SO2比值的不同变化趋势。结果表明,早在20世纪90年代中期,长江三角洲酸性气体污染水平已经较高,其后主要是NOx浓度显著升高,从而使该地区成为硫和氮污染并重的地区;东北平原酸性气体过去浓度很低,但这些气体以很高的速率增长,虽然目前浓度水平仍然比较低,但未来形势不容乐观。     

Contact angles in CO2-water-coal systems at elevated pressures

Injection of carbon dioxide into coal seams is considered to be a potential method for its sequestration away from the atmosphere. However, water present in coals may retard injection: especially if carbon dioxide does not wet the coal as well as water. Thus contact angles in the coal-water-CO₂ system were measured using CO₂ bubbles in water/coal systems at 40 °C and pressures up to 15 MPa using five bituminous coals. At low pressures, in this CO₂/water/coal system, receding contact angles for the coals ranged between 80° to 100°; except for one coal that had both high ash yield and low rank, with a contact angle of 115°, indicating that it was hydrophilic. With increasing pressure, the receding contact angles for the different coals decreased, indicating that they became more CO₂-wetting. The relationship between contact angle and pressure was approximately linear. For low ash or high rank coals, at high pressure the contact angle was reduced to 30-50°, indicating the coals became strongly CO₂-wetting; that is CO₂ fluids will spontaneously penetrate these wet coals. In the case of the coal that was both high ash and hydrophilic, the contact angle did not drop to 90° even at the highest pressures used. These results suggest that CO₂ will not be efficiently adsorbed by all wet coals equally well, even at high pressure. It was found that at high pressures (> 2 MPa) the rate of penetration of carbon dioxide into the coals increased rapidly with decreasing contact angle, independently of pressure. Injecting CO₂ into wet coals that have both low rank and high ash will not trap CO₂ as well as injecting it into high rank or low ash coals.     

燃煤烟气中SO2治理方法综述

对燃煤烟气中SO2的脱除方法进行综述和分析。