Adsorption of Au(III) and Au(I) complexes on δ-MnO2

The sorption of AuCl₄ ⁻,AuCl₂ ⁻ and Au(S₂O₃)^3- on δ-MnO₂ was investigated at pH2–11.6, 0.01 mol/L and 0.1 mol/L NaNO₃ solutions. At pH 4 in two electrolyte strength solutions, Au sorption densities on δ-MnO₂ are 0.18–0.21 and 0.28μmoL/m² for AuCl₄ ⁻ and Au(S₂O₃)₂ ^3-, respectively, and the Au surface coverage is approximate to or lower than 1%. This adsorption of the two Au complexes decreases as the solution pH increases, which conforms to the sorption regularity of the anion on δ-MnO₂. The Au sorption decreases in the sequence of Au(S₂O₃)₂ ^3- >AuCl₄ ⁻ >AuC1₂ ⁻. The intrinsic equilibrium constants (logK ^int) of the three Au complexes are 1.17–2.7, much higher than those of Cu and Cd. The hydrolysis products of AuCl₄ ^- are preferentially adsorbed by δ-MnO₂ and the inner-sphere Au-surface complexes are formed on the surface. Project supported by the National Studying-abroad Foundation, the National Natural Science Foundation of China (Grant No. 49573200) and the Australian Mining Industry.     

Middle and Late Devonian microbial carbonates,reefs and mounds in Guilin,South China and their sequence stratigraphic,paleoenvironmental and paleoclimatic significance

The importance of calcimicrobes and microbialite in carbonate platform and reefal environments has been stressed in recent literature. Burne and Moore[1] introduced the term microbialite to describe the clotted, laminated and undifferentiated fabrics formed by mi-crobial communities. Microbialites are organosedi-mentary deposits that have accreted as a result of ben-thic (prokaryotic or eukaryotic) communities, trapping and binding detrital sediment[1]. Microbial organisms and microbialite are…     

Adsorption of As on hydroxy-Fe-montmorillonite complexes

DOI: 10.1360/03yd0553 Arsenic, a toxic element, is ubiquitous in the earth’s crust and may lead to health risks for humans. This may come about as a result of oxidative weathering and dissolution of As-containing minerals, use of ar-senical pesticides, excess use of some fertilizers and from mine drainage, smelter wastes and agricultural drainage water from certain arid regions. The dis-solved inorganic arsenic is transported in surface or2156 Science in China Ser. D Earth Sciences groun…     

Surface area, porosity and water adsorption properties of fine volcanic ash particles

Our understanding on how ash particles in volcanic plumes react with coexisting gases and aerosols is still rudimentary, despite the importance of these reactions in influencing the chemistry and dynamics of a plume. In this study, six samples of fine ash (<100 m) from different volcanoes were measured for their specific surface area, a_s, porosity and water adsorption properties with the aim to provide insights into the capacity of silicate ash particles to react with gases, including water vapour. To do so, we performed high-resolution nitrogen and water vapour adsorption/desorption experiments at 77 K and 303 K, respectively. The nitrogen data indicated a_s values in the range 1.1–2.1 m²/g, except in one case where a a_s of 10 m²/g was measured. This high value is attributed to incorporation of hydrothermal phases, such as clay minerals, in the ash surface composition. The data also revealed that the ash samples are essentially non-porous, or have a porosity dominated by macropores with widths >500 Å. All the specimens had similar pore size distributions, with a small peak centered around 50 Å. These findings suggest that fine ash particles have relatively undifferentiated surface textures, irrespective of the chemical composition and eruption type. Adsorption isotherms for water vapour revealed that the capacity of the ash samples for water adsorption is systematically larger than predicted from the nitrogen adsorption a_s values. Enhanced reactivity of the ash surface towards water may result from (i) hydration of bulk ash constituents; (ii) hydration of surface compounds; and/or (iii) hydroxylation of the surface of the ash. The later mechanism may lead to irreversible retention of water. Based on these experiments, we predict that volcanic ash is covered by a complete monolayer of water under ambient atmospheric conditions. In addition, capillary condensation within ash pores should allow for deposition of condensed water on to ash particles before water reaches saturation in the plume. The total mass of water vapour retained by 1 g of fine ash at 0.95 relative water vapour pressure is calculated to be ~10^–2 g. Some volcanic implications of this study are discussed.Editorial responsibility: J. Gilbert     

短期增温和降水减少对沙质草地土壤微生物量碳氮和酶活性的影响

通过模拟气候变化,探究短期增温和降水减少对沙质草地土壤微生物量碳氮及酶活性的影响,揭示沙质草地土壤微生物量碳氮和酶活性对短期气候变化的响应规律。结果表明：（1）短期增温和降水减少对土壤微生物量碳氮和酶活性均产生显著影响。（2）在自然温度下,与自然降水相比,降水减少40%时土壤微生物量碳（MBC）和微生物氮（MBN）含量最高,增幅分别为87.9%和98.8%;降水减少60%时土壤碱性蛋白酶（S-ALPT）活性最低,降幅达32.8%。（3）在增温条件下,与自然降水相比,降水减少40%时土壤MBC和MBN含量最低,降幅分别为25.67%和48.16%,土壤脲酶（S-UE）活性最高,增幅20.42%。（4）土壤pH与3种土壤酶活性正相关,与土壤微生物量碳氮负相关。土壤微生物量碳氮与土壤纤维素酶（S-CL）活性负相关,与S-UE、S-ALPT活性正相关。     

斜纤蛇纹石的管道水特征研究

河北涞源斜纤蛇纹石为较小的中孔纳米管材料,通过氮吸脱附法、差热和热重曲线分析法、差示扫描量热分析法和红外光谱分析法,主要分析了其纳米管中管道水特征,明确了管道水作为有效加速剂和载体的作用,对以及对抗拉强度和介电常数的影响。研究表明斜纤蛇纹石纳米管中存在管道水(属于吸附水),去除温度在240℃±,内径为2nm～3nm的纳米管中管道水含量最高,管道水含量与纳米管分散度成反比。     

构造煤结构与煤层气赋存研究进展

碎软煤的完整原样制取困难,需要加工制成重塑煤体,为了研究不同压制荷载对煤体物性特征的影响,以重塑煤体为研究对象,基于低温液氮的孔隙测试实验和高压容量法的甲烷吸附实验,探讨不同成型荷载而成的重塑煤体的微小孔结构及其吸附特性的差异。结果表明：不同成型荷载压制而成的重塑煤体,其微孔和小孔的孔容随着成型荷载的增大而略微减少,孔比表面积随着成型荷载的增大而略微增加,总孔体积减少和孔比表面积增加的幅度不大;通过分形理论发现无论高压段还是低压段,孔隙结构具有明显的分形特征,且在高压段的分形维数普遍低于低压段,不同荷载压制而成的重塑煤体的分形维数差别不大;等温吸附线均符合第Ⅰ类等温吸附曲线,Langmuir模型适用于描述重塑煤体的等温吸附,成型荷载对煤的吸附常数有一定的影响,其对吸附常数b值的影响大于对a值的影响。研究不同成型荷载下重塑煤体的吸附特性,为不同条件下型煤制作及冷冻取心实验提供参考。     

下三叠统鲕粒灰岩中微生物矿化组构特征及意义 ——以川东北地区飞仙关组为例

PTB全球最大生物灭绝事件后,早三叠世被认为是微生物发育繁殖的黄金时期,浅水环境是微生物活动及微生物岩形成的最有利环境。借助高分辨率扫描电镜和能谱分析,在川东北地区开江—梁平海槽西侧下三叠统飞仙关组浅水碳酸盐岩台地边缘的鲕粒灰岩中发现了三种微生物矿化组构:空腔状微生物矿化组构、显微瘤状微生物矿化组构和纤状微生物矿化组构;通过沉积学、岩石学及地球化学的综合分析,认为显微瘤状微生物矿化组构是微生物新陈代谢时形成的纳米球状云质颗粒,纤状微生物矿化组构是微生物的胞外聚合物,而空腔状微生物矿化组构则属于微生物个体。这些微生物矿化组构的发现,为早三叠世微生物大爆发提供了一定的直观证据;推测大量的微生物活动是早三叠世碳酸盐快速沉积现象的直接诱因,并导致于二叠纪末发育的克拉通内裂陷——开江—梁平海槽在早三叠世被快速填平。     

脱气温度和样品粒径对致密砂岩低温氮气吸附实验结果的影响

基于静态体积法的低温氮气吸附实验已广泛用于分析致密储集层的孔隙结构。本文探索了脱气温度和样品粒径对松辽盆地高台子致密砂岩低温氮气吸附实验结果的影响。结果显示,110℃的脱气条件并不能清除束缚水而使得孔隙体积、比表面积均偏低,300℃的脱气条件容易破坏样品中黏土矿物的结构令孔隙体积、比表面积减小,200℃是比较合适的脱气温度,既能去除束缚水又不破坏黏土矿物结构。样品粒径从5～10目减小至10～30目,氮气探测的孔隙数量增多使比表面积、孔体积增大。从10～30目减小至180～200目,黏土矿物相对含量降低令比表面积、孔体积显著减小;小于200目的样品中减少的黏土矿物主要集中在大于200目的岩样中,因此大于200目岩样的测定结果最高。因此,10～30目是利用低温氮气吸附实验寻求分析致密砂岩储集层特征的最佳粒径范围。