煤显微组分中有机硫的微区分析和分布特征

应用扫描电镜、能谱仪和波谱仪测定了煤中有机硫含量。a.在镜质体有机硫含量低于0.50％的煤中,惰质体的有机硫含量与其相近。而在镜质体有机硫含量高于0.5％的煤中,惰质体的有机硫含量大多为镜质体的40％～50％。各种镜质体和惰质体的有机硫含量随其凝胶化程度增高而增加。b.聚煤古地理环境对煤中有机硫含量起决定性作用。以镜质体为例,形成于湖滨三角洲平原环境的神木煤含有机硫0.21％,形成于滨海三角洲平原环境的水城大河边煤含有机硫0.84％,形成于泻湖海湾环境的兖州晚石炭世煤含有机硫2.24％。     

微波炉在重量法测定硫中的应用

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。     

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

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。     

融入WTO——为农业服务的化工矿产资源发展战略构想

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。     

阿尔泰地区铜镍矿床综合信息找矿模型及成矿预测

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。     

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

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。     

胶东金矿集区硫和碳的循环与控矿作用

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.     

The Kuwae (Vanuatu) eruption of<Emphasis Type="SmallCaps"> AD</Emphasis> 1452: potential magnitude and volatile release

Sometime during AD 1452, according to new evidence, a large-magnitude, initially phreatomagmatic eruption, destroyed the island of Kuwae (16.83°S, 168.54°E), located in the present-day Republic of Vanuatu. It created a 12×6-km submarine caldera composed of two adjacent basins. Based on estimates of caldera volume, between 30 and 60 km³ DRE of dacite magma was ejected as pyroclastic flow and fall deposits during this event. Annual layers of ice dating from the period AD 1450–1460 contain acidity peaks representing fallout of sulfuric acid onto both the Greenland and Antarctic ice caps. These acidity peaks have been attributed by others to the sedimentation of H₂SO₄ aerosols that originated from sulfur degassing during the Kuwae eruption. Improved dating techniques and new data from nineteen ice cores reveal a single acidity peak attributed to Kuwae lasting from 1453 to 1457. In this study, we present new electron microprobe analyses of the S, Cl, and F contents of matrix glasses and glass inclusions in phenocrysts from tephra ejected during the Kuwae eruption. We establish that the Kuwae event did indeed yield a large release of sulfur gases. From our glass inclusion data and analysis, we calculate that the total atmospheric aerosol loading from the 1452 Kuwae eruption was ≫100 Tg H₂SO₄. Much of the volatile mass released during the eruption was probably contained in a separate, volatile-rich, fluid phase within the pre-eruptive Kuwae magma body. Comparing the volatile release of the Kuwae eruption with other large-magnitude eruptions, places Kuwae as the greatest sulfuric acid aerosol producer in the last seven centuries, larger even than sulfur emissions from the eruption of Tambora (Indonesia) in 1815, and possibly Laki (Iceland) in 1783. The severe and unusual climatic effects reported in the mid- to late-1450s were likely caused by the Kuwae eruption.     

Do stratocumulus clouds detrain? FIRE I data revisited

Analyses of aircraft observations of the stratocumulus-topped boundary layer during the First ISCCP (International Satellite Cloud Climatology Project) Regional Experiment (FIRE I) show the frequent presence of clear, but relatively moist, air patches near the stratocumulus cloud-top interface. A conditional sampling of measurements in these clear air patches shows that their thermodynamic properties do more resemble boundary-layer air characteristics than those of free troposphere air. From an aircraft leg through cloud tops it is demonstrated that turbulent mixing across the cloud-top interface can lead to the local dissipation of the cloud top. Analogous to the terminology used for shallow cumulus parameterizations this process can be considered as detrainment, with which we mean that after a mixing event across the cloud-top boundaries, mixed unsaturated parcels become part of the clear environment of the cloud.