云南地下水中Rn和Hg震兆特征对比分析

以大量的实际观测资料及多次震例 ,深入研究了地下水中Rn和Hg的震兆特征。结果表明 :Hg对地壳岩石应力应变的反应程度比Rn更灵敏 ,更有利于地震预报。通过研究得出以下几点认识 :(1)大震前 ,Hg有 1年左右的中期趋势异常且都出现在距震中较近的有利部位 ,Rn有 1— 2年的趋势异常出现在距震中 5 0 0km范围内 ;(2 )大震前 ,大多数观测台站能观测到Hg突出的短临异常 ,而Rn出现短临异常的台站数只有Hg的1/ 2 ,且异常幅度小 ;(3)中强地震前 ,在距震中较近的观测台站 ,能观测到Hg异常 ,相同条件下的Rn异常则不明显。地下水中Rn和Hg的这些异常特征对未来地震三要素的预报有一定帮助。     

The Lanmuchang Tl deposit and its environmental geochemistry

Tl is a dispersed element and it seldom occurs in the form of independent minerals.The world annual production of Tl is about 13 ton, most of which is by-product separated from non-ferrous metal products. Lanmuchang is the only large-size independent Tl deposit in the world. Bio-enrichment and hydrothermal reworking are the two important metallogenic mechanisms of this Tl deposit. Samples of plant and animal organs and villagers’ urine as well as hair and nail (toenail) samples from the Tl mining district were analyzed. Analytical results showed that the contents of Tl, Hg and As are high, suggesting that the residents and villagers in the mining district have been affected by Tl-Hg pollution, and on the other hand, they can serve as the guidelines for ore prospecting. The contents of Tl, Hg, and As in human beings and other organic bodies depend largely on the background values of these metals in rock, ore, soil and water.     

鄂尔多斯盆地延长组超低渗透砂岩储层微观孔隙结构特征研究

通过物性分析、扫描电镜、铸体薄片、高压压汞技术对鄂尔多斯盆地延长组沿25、庄40、庄19三个区块超低渗透砂岩储层样品进行分析测试,研究其微观孔隙结构特征。研究表明,超低渗透砂岩储层岩石孔隙结构非均质性强,孔隙喉道类型多样是储层渗透性差的主要原因;孔喉分选系数在2.0~2.5之间、变异系数在0.1~0.2之间物性较好;较大孔喉是决定和改善储层渗透性的重要因素,细小孔道对储层储集能力的贡献较大,储层微裂缝较为发育。储层物性参数的差异、孔喉特征参数的差异等,均归因于微观孔隙结构的差异。     

天然磁铁矿处理含Hg（Ⅱ）废水实验研究

利用重金属离子可在水合金属氧化物和氢氧化物矿物表面产生吸陵作用的原理，进行了天然磁铁矿处理含Hg(Ⅱ）废水的实验研究，结果表明：当温度为25℃，吸附平衡时间为60分钟、试样用量为20g/L，试样粒径为200目以下、pH值为6.40，离子强度为零时，Hg(Ⅱ）初始浓度为1.12mg/L的溶液的吸附率可达98%，使废水中Hg(Ⅱ）的浓度达到国家排放标准。pH值、离子强度、粒径、试样用量、废水浓度、温度、时间均对Hg(Ⅱ）的吸附率有一定的影响，其中pH值的影响最大，Hg(Ⅱ）在天然磁铁矿上的吸附等温曲线不同于Langmuir和Freundlich等温曲线，而是表现为台阶段，符合分级离子/配位子交换等温曲线。     

从汞异常讨论阳江——从化断裂的活动性及对孕震的影响

根据区域重砂普查圈定的辰砂分散晕和跨断层剖面壤中气汞测量结果，联系已有地震资料，讨论了阳江－－从化断裂带的活动性及汞异常与地震活动的关系。认为：沿断裂 带群集的汞民中以作为活动断裂的判别标志之一；汞沿断裂裂隙向上运移系促使断裂活动的动力因素之一；汞异常段之间的相对低值区或其外侧系地震活动的主要场所。     

Mechanism of Hg(II) immobilization in sediments by sulfate-cement amendment

Reactive amendments such as Portland and super-sulfate cements offer a promising technology for immobilizing metalloid contaminants such as mercury (Hg) in soils and sediments through sequestration in less bioavailable solid forms. Tidal marsh sediments were reacted with dissolved Hg(II) in synthetic seawater and fresh water solutions, treated with Portland cement and FeSO₄ amendment, and aged for up to 90 days. Reacted solids were analyzed with bulk sequential extraction methods and characterized by powder X-ray diffraction (XRD), electron microscopy, and synchrotron X-ray absorption spectroscopy at the Hg L_III- and S K-edge. In amended sediments, XRD, SEM and sulfur K-edge XANES indicated formation of gypsum in seawater experiments or ettringite-type (Ca₆Al₂(SO₄)₃(OH)₁₂^.26H₂O) phases in fresh water experiments, depending on the final solution pH (seawater ∼8.5; freshwater ∼10.5). Analysis of Hg EXAFS spectra showed Cl and Hg ligands in the first- and second-coordination shells at distances characteristic of a polynuclear chloromercury(II) salt, perhaps as a nanoparticulate phase, in both seawater and fresh water experiments. In addition to the chloromercury species, a smaller fraction (∼20–25%) of Hg was bonded to O atoms in fresh water sample spectra, suggesting the presence of a minor sorbed Hg fraction. In the absence of amendment treatment, Hg sorption and resistance to extraction can be accounted for by relatively strong binding by reduced S species present in the marsh sediment detected by S XANES. Thermodynamic calculations predict stable aqueous Hg–Cl species at seawater final pH, but higher final pH in fresh water favors aqueous Hg-hydroxide species. The difference in Hg coordination between aqueous and solid phases suggests that the initial Hg–Cl coordination was stabilized in the cement hydration products and did not re-equilibrate with the bulk solution with aging. Collectively, results suggest physical encapsulation of Hg as a polynuclear chloromercury(II) salt as the primary immobilization mechanism.     

Variations of levels and composition of PM10 and PM2.5 at an insular site in the Western Mediterranean

The insular suburban site of Castillo de Bellver was selected for the study of the variability of PM levels and composition in the Western Mediterranean Basin (WMB).Mean annual (in 2004) PM₁₀ and PM_2.5 levels at this site were 29 and 20 µg/m³, respectively. These levels may be regarded as relatively low when compared with other suburban insular locations in the Eastern Mediterranean Basin (EMB), but they are higher than those recorded at most of the European suburban sites, especially in Northern and Western Europe. Seasonal variability of PM levels at this site is governed by meteorology rather than local emissions, whereas the daily cycles are clearly defined by the anthropogenic emissions, mainly coming from the urban area of Palma de Mallorca and the harbour area of the same city.Concerning the aerosol composition at this site, the main PM constituent is the mineral matter (29% in PM₁₀ and 16 % in PM_2.5), more than 50% (in PM₁₀) being attributable to African dust. The amount of secondary inorganic aerosols is also very high (27% in PM₁₀ and 34% in PM_2.5), with the predominance of fine ammonium sulphate, and in a less proportion fine ammonium nitrate (in winter) and coarse Ca and Na nitrate (with higher importance in summer). The carbonaceous particles, dominantly fine, account for 17% of PM₁₀ and 25% of PM_2.5. The elemental carbon/organic carbon (EC/OC) ratio reached a mean value of 0.17, similar to those observed at regional background sites in the WMB coast of Spain. The sea spray aerosols (mainly coarse) represented around 10% of PM₁₀, and only 4% in PM_2.5. Finally, the unaccounted fraction increased from 15% to 20% in PM_2.5, being mostly attributed to water.The concentrations of trace elements in PM₁₀ and PM_2.5 were usually in the range to those observed in regional background sites in the Iberian Peninsula, with the exception of the typical tracers of road traffic such as Cu, Sb, Zn, Sn and Ba, which presented concentrations in the range of urban sites of Iberia. Other elements such as Cr, Zr, Hf and Co have been identified as the main tracers of the harbour contributions.     

新矿物——铊明矾

铊明矾 (lanmuchangite ,TlAl[SO4]2 ·12H2 O)是在贵州滥木厂铊 (汞 )矿床富铊矿体氧化带中发现的一种铊的硫酸盐新矿物。该矿物为产于氧化带的次生矿物 ,其共生矿物为水绿矾、镁铝矾、钾明矾、黄钾铁矾、石膏、自然硫、砷华及某些未知矿物。其矿物集合体大小一般为 2～ 10mm ,集合体多为致密块状 ,单晶呈他形粒状 ,4 0～ 90 μm ,偶见平行柱状集合体 ,半自形至自形柱状晶体 ,直径 15～ 65 μm。白色至淡黄色 ,玻璃光泽 ,透明 ,易溶于水。偏光显微镜下无色 ,均质体 ,实测折光率为 1.4 95。维氏硬度为 94～ 12 4kg/mm2 ,摩氏硬度为 3 .1～ 3 .4 ,实测密度 2 .2 2 g/cm3。平均化学成分 :Tl2 O =3 3 .2 5 % ,Al2 O3=8.0 7% ,SO3=2 5 .19% ,SiO2=0 .10 % ,K2 O =0 .3 5 % ,CaO =0 .0 8% ,MgO =0 .0 6% ,FeO =0 .0 4 % ,H2 O =3 3 .4 6% ,总和 10 0 .60 % ,除结晶水由热重分析 (TG)求得 ( 3件样品平均 )外 ,其余成分均由电子探针分析 ( 6点平均 )求得。化学式为(Tl1.0 0 K0 .0 5) 1.0 5(Al1.0 1Si0 .0 2 Ca0 .0 1Mg0 .0 1Fe0 .0 1) 1.0 6 [SO4]2 .0 2 ·11.86H2 O ,理论式为TlAl[SO4]2 ·12H2 O。X射线粉末衍射主要强线 [d(I,hkl) ]为 :0 .4 3 14 ( 10 0 ,2 2 0 ) ,0 .2 80 1( 70 ,3 3 1) ,0 .70 3 ( 5 4 ,1     

黔西南、桂北地区微细浸染型金矿床砷、锑、汞、铊元素及矿物组合特征

本文结合野外地质调查和有关的低温硫化物相平衡实验结果，对黔西南、桂北地区的浅成低温热液浸染型金矿床中与金共（伴）生的硫化物矿物组合、地球化学特征及其成矿作用机制进行了综合分析研究。研究表明，与金矿化共（伴）生的砷、锑、汞和铊等地球化学指示元素及其矿物组合不仅具有成生方面的联系，而且可以作为寻找金的一种特征的标型标志。     

成都市土壤测量Hg元素的发育特征及其来源

成都市是Hg的高背景和民异常区，深、浅层样各具不同的元素组合和发育特征。深层样Hg异常与构造、天然气、地热、矿产和基底隆起有关；浅层样则与城市居民生活，古代颜料、工业、燃煤、农业、河流的污染及上游的矿产等物质来源有关。