热水溶液地球化学   总被引：8，自引：0，他引：8  

曾贻善 《地学前缘》1996,3(3):89-95

概述了热水溶液地球化学的主要研究内容和近年来在实验和理论研究方面的进展，包括高温高压下水的热力学性质、状态方程式、介电常数、电导率和电离平衡；ＮａＣｌ－ＣＯ２－Ｈ２Ｏ体系及其边界体系（ＮａＣｌ－Ｈ２Ｏ和ＣＯ２－Ｈ２Ｏ）的相关系、热力学性质和状态方程式，特别是利用人工流体包裹体技术和分子动力学模拟取得的新成果；高温高压电解质稀水溶液的电导测定；以ＨＫＦ模型为基础，热水溶液中不同物种的标准偏摩尔热力学性质和高温高压有关物理化学参数的估算；热水溶液中的物种形成（热液流体中的矿物溶解度测定、电势测量和谱学研究）；水和热水溶液结构的红外和拉曼谱学研究；水和热水溶液的传输性质（粘度和导热系数）。  相似文献   

云南金顶超大型铅锌矿区水系沉积物中镉的形态分析     

李航  肖唐付  朱长生  何立斌  宁增平  李大华  双燕  谭显龙 《矿物岩石》2008,28(2):107-112

金顶矿区长期的矿业活动造成矿区水系沉积物严重污染.通过沉积物中Cd的化学形态分析发现:矿区沉积物中Cd元素形态主要以可还原态为主,其次为可氧化态Cd、残渣态Cd和弱酸提取态Cd.沉积物中Cd的形态特征受污染源的控制.当沉积物受氧化矿为主体的污染源控制时,镉的弱酸提取态和可还原态相对较高(占总金属量的90%以上),而当沉积物受硫化矿为主体污染源控制时.镉的弱酸提取态和可还原态相对较低(仅占总金属量的20%左右).池江水系沉积物中Cd的弱酸提取态占相当大比例(占金属总量的18.8%),在表生环境中极易释放出来并污染水体,对矿区乃至矿区下游流域生态环境构成直接的危害.  相似文献   

环境中硒形态分析方法的研究进展   总被引：2，自引：0，他引：2  

秦海波  朱建明  李社红  雷磊  尚林波 《矿物岩石地球化学通报》2008,27(2)

硒的形态研究是了解环境中硒的毒性、生物可利用性、迁移和生物地球化学循环等方面的基础,其研究方法一般分为直接和间接法。本文总结了环境中硒形态的研究方法,特别是对环境样品中常用的硒形态分析技术——连续化学浸提技术作了全面详细的讨论,并综述了其它硒形态分析方法的最新动态。  相似文献   

Characteristics of Chemical Speciation in PM_1 in Six Representative Regions in China     

Kaixu BAI  Can WU  Jianjun LI  Ke LI  Jianping GUO  Gehui WANG 《大气科学进展》2021,38(7):1101-1114

A better knowledge of aerosol properties is of great significance for elucidating the complex mechanisms behind frequently occurring haze pollution events. In this study, we examine the temporal and spatial variations in both PM_1 and its major chemical constituents using three-year field measurements that were collected in six representative regions in China between 2012 and 2014. Our results show that both PM_1 and its chemical compositions varied significantly in space and time, with high PM_1 loadings mainly observed in the winter. By comparing chemical constituents between clean and polluted episodes, we find that the elevated PM_1 mass concentration during pollution events should be largely attributable to significant increases in organic matter(OM) and inorganic aerosols like sulfate, nitrate, and ammonium(SNA),indicative of the critical role of primary emissions and secondary aerosols in elevating PM_1 pollution levels. The ratios of PM_1/PM_(2.5) are found to be generally high in Shanghai and Guangzhou, while relatively low ratios are seen in Xi'an and Chengdu, indicating anthropogenic emissions were more likely to accumulate in forms of finer particles. With respect to the relative importance of chemical components and meteorological factors quantified via statistical modeling practices, we find that primary emissions and secondary aerosols were the two leading factors contributing to PM_1 variations, though meteorological factors also played important roles in regulating the dispersion of atmospheric PM.  相似文献   

海水养殖池沉积物中重金属形态和生物酶活性的关系研究   总被引：1，自引：0，他引：1  

李玉  高焕  刘付程 《海洋与湖沼》2016,47(1):83-90

以连云港市对虾养殖池表层沉积物为研究对象,采用Tessier连续萃取法,研究了表层沉积物中重金属(Cu、Zn、Pb、Cd、Cr、As、Mn)的赋存形态和酶(脲酶、碱性磷酸酶、过氧化氢酶、转化酶)活性的相关性。结果表明,重金属Cu和Zn以有机-硫化物结合态为主要的赋存形态,Pb以铁锰氧化物态为主要的赋存形态,Cd以可交换态(平均33.47%)和碳酸盐结合态(平均31.16%)为主要存在形态,Cr和As主要以残渣态存在,Mn的铁锰氧化物态比例最高。脲酶的活性范围为0.45—8.96mg/(g·24h),碱性磷酸酶活性范围为2.45—6.69mg/(g·24h),过氧化氢酶活性范围为0.14—2.36m L/(g·min),转化酶活性范围为0.45—10.45mg/(g·24h)。脲酶活性与Cd、As的可交换态、Cd的碳酸盐结合态、Cu、As的铁锰氧化物态、Zn、Pb、Cd、Mn的有机硫化物态之间显著相关;碱性磷酸酶活性与Zn、Cd的铁锰氧化物态显著相关;过氧化氢酶活性与Cd的可交换态、碳酸盐结合态及残渣态、Cu、Cd、As的铁锰氧化物态、Zn、Pb、Cd、Mn的有机硫结合态之间显著相关;转化酶活性与Cu、Cd、As的可交换态、Cd的碳酸盐结合态、Cu、Cd、As的铁锰氧化物态、Zn、Pb、Cd、Mn的有机硫化物态、Cd、As的残渣态之间显著相关。酶活性可以用来指示海水养殖池沉积物中重金属的形态转化过程。  相似文献   

Sulfur speciation in marine sediments impacted by gas emissions in the northern part of the South China Sea     

《Marine and Petroleum Geology》2016

Three cores of marine sediments from the Shenhu area in the northern part of the South China Sea were analyzed by XANES analysis for sulfur speciation. The area has been investigated for the presence of hydrocarbons and potential gas hydrate formations. Cored samples of site 4B showed a specific profile of sulfur speciation with sharp and frequent variations in relative contents of sulfate and sulfide, which differed greatly from the profiles obtained for the sediments taken at sites 5B and 6A. The upper part of core 4B (of 0–95 cm) was soft and rich in pore water, containing mainly coarse silt sand. The lower part of the core (i.e., depth > 95 cm) was relatively dryer and darker in color, and dominated by silts and clay resembling sediments from mud volcanoes. The sulfur speciation results revealed that sulfate makes up almost 100 percent of all sulfur species in the upper part of the core 4B, which indicates strong oxidizing conditions, whereas the lower part of the same core has high relative contents of sulfide, sometimes close to 100% S²⁻. In the lower part of the core, the relative content of sulfide and sulfate changes rapidly and frequently, indicating rapid changes of oxidizing and reducing conditions. On the other hand, the vertical profiles of sulfur species for the cores from sites 5B and 6A are relatively consistent with lower sulfide contents indicative of stable and weaker reducing conditions. We hypothesize that the frequent and sharp variations in the ratios of sulfide to sulfate at site 4B may indicate some intermittent eruption of methane with clay from petroleum reservoirs underneath the sea floor over a relatively short period of time.  相似文献   

Experiments on the Element Distribution between the Granodiorite JG-1a and 2M NaCl Hydrothermal Solution at Temperatures of 300 to 800°C and a Pressure of 1 kb     

Etsuo Uchida    Takuro Haitani    Takayuki Suetsugu    Takahiro Kashima  Ken Tsutsui 《Resource Geology》2003,53(2):155-161

Abstract. The distribution of Na, K, Ca, Mg, Mn and Fe between the granodiorite JG-la, one of the geochemical standard rocks, and 2M NaCl aqueous solution was experimentally determined at temperatures of 300 to 800C and a pressure of 1 kb using standard cold seal-type pressure vessels. The solid run products melted partially at 800C. Only K shows a significantly different behavior from the experiments using the basalt JB-la (Uchida and Tsutsui, 2000) due to the presence of ortho-clase in the JG-la. The transition elements tend to be preferably partitioned into the aqueous chloride solutions with increasing temperature. At 800C and 1 kb, the Fe concentration of the aqueous chloride solutions reached up to 5,000 ppm, and the Mn concentration up to 350 ppm. The distribution coefficient, K_{D, i} = C_{i, sol}/C_i, rock, is in the order of Na>K>Mn>Ca> Fe>Mg at 300C, but changed in the order of Mn>N>K>Fe>Ca>Mg at 800C. The distribution coefficients of the divalent cations for the JG-la are higher than those for the JB-1a. The distribution coefficient of the transition elements, Fe and Mn, increases significantly with increasing temperature. The thermodynamic analysis for aqueous speciation revealed that this is attributable to the formation of the tri-chloro complexes of the transition elements at higher temperatures.  相似文献   

阳山伊利石表面化学特性及化合态   总被引：1，自引：0，他引：1  

吴大清  刁桂仪  彭金莲 《矿物岩石》2003,23(3):1-4

用非连续酸碱滴定法和氯化铵-乙醇法测定表明,2M1型伊利石的pHzpc＝6.5,阳离子交换量CEC＝11.0×105mol/g.应用恒容双表面位模式,通过多元非线性拟合计算表明,伊利石表面铝醇基＞AlOH浓度N1,Al＝4.0×10-5mol/g,质子化常数pKal,Al＝5.95和pKa2,Al＝9.45,硅醇基＞SiOH的Nt.si＝0.53×10-5mol/g,pKa2,si＝3.85.同时发现,在伊利石表面酸碱特性研究中,当溶液pH＜4时,须考虑伊利石表面阳离子与溶液质子之间的交换反应,测定表明交换反应常数Kx＝0.42.  相似文献   

Organic carbon to Th ratios of marine organic matter     

U. Passow  J. Dunne  J.W. Murray  L. Balistrieri  A.L. Alldredge 《Marine Chemistry》2006,100(3-4):323

Uncertainties in the determinations of particulate organic carbon flux from measurements of the disequilibrium between ²³⁴Th and its mother isotope uranium depend largely on the determination of the organic carbon to ²³⁴thorium (OC : ²³⁴Th) ratio. The variability of the OC : ²³⁴Th ratio in different size fractions of suspended matter, ranging from the truly dissolved (< 3 or 10 kDa) fraction to several millimeter sized marine snow, as well as from sediment trap material was assessed during an eight-day cruise off the coast of California in Spring 1997. The affinity of polysaccharide particles called TEP (transparent exopolymer particles) and inorganic clays to ²³⁴Th was investigated through correlations. The observed decrease in the OC : ²³⁴Th ratio with size, within the truly dissolved to small particle size range, is consistent with concepts of irreversible colloidal aggregation of non-porous nano-aggregates. No consistent trend in the OC : ²³⁴Th ratio was observed for particles between 1 or 10 to 6000 μm. Origin and fate of marine particles belonging to this size range are diverse and interactions with ²³⁴Th too complex to expect a consistent relationship between OC : ²³⁴Th ratio and size, if all categories of particles are included. The relationship between OC and ²³⁴Th was significant when data from the truly dissolved fraction were excluded. However, variability was very large, implying that OC flux calculations using different collection methods (e.g. sediment trap, Niskin bottles or pumps) would differ significantly. Therefore a large uncertainty in OC flux calculations based on the ²³⁴Th method exist due to individual decisions as to which types or size classes of particles best represent sinking material in a specific area. Preferential binding of ²³⁴Th to specific substance classes could explain the high variability in the relationship between OC and ²³⁴Th. At 15 m, in the absence of lithogenic material, the OC : ²³⁴Th ratio was a function of the fraction of TEP or TEP-precursors in OC, confirming that acidic polysaccharides have a high affinity for ²³⁴Th and that TEP carry a ligand for ²³⁴Th. Preferential binding to TEP might change distribution patterns of ²³⁴Th considerably, as TEP may sink when included in large aggregates, or remain suspended or even ascend when existing as individual particles or microaggregates. In the presence of lithogenic matter, at depths below 30 m, the ratio between ²³⁴Th and OC was linearly related to the ratio between alumino silicates and C. The affinity of inorganic substances to ²³⁴Th is known to be relatively low, suggesting that a coating of acidic polysaccharides was responsible for the apparently high affinity between ²³⁴Th and lithogenic material. Overall, OC : ²³⁴Th ratios of all material collected during this investigation can best be explained by differential binding of ²³⁴Th to both TEP and TEP-precursors, as well as to lithogenic minerals, which were very abundant in an intermediate nepheloid layer between 50 and 90 m.  相似文献   

Morphometric or morpho-anatomal and genetic investigations highlight allopatric speciation in Western Mediterranean lagoons within the Atherina lagunae species (Teleostei, Atherinidae)     

M. Trabelsi  F. Maamouri  J.-P. Quignard  M. Boussaïd  E. Faure   《Estuarine, Coastal and Shelf Science》2004,61(4):713-723

Current distribution of Atherina lagunae poses an interesting biogeographical problem as this species inhabits widely separate circum-Mediterranean lagoons. Statistical analyses of 87 biometric parameters and genetic variation in a portion of the cytochrome b gene were examined in four populations of A. lagunae from Tunisian and French lagoons. The results suggested a subdivision into two distinct Atherinid groups: one included the French lagoonal sand smelts and the second included the Tunisian ones. Tunisian lagoonal sand smelts were distinguished from the French ones by the lower number of lateral line scales, vertebrae, pectorals and first dorsal fin rays and the higher number of lower and total gillrakers. In addition, A. lagunae from Tunisian lagoons are characterised by short preorbital length, developed operculum, broad interorbital space, larger head, robust body and a relatively small first dorsal fin which is positioned backwards. In addition, intraspecific sequence variation in a portion of the cytochrome b gene was examined in 87 individuals from Tunisia and France. The high correlation between the results of the molecular phylogenetic tree and biometric statistical data analysis suggested that two different sibling species or at least sub-species or semi-species have colonised the lagoons. In addition, our analyses suggested that the evolution of A. lagunae probably occurred in two steps including marine sympatric speciation within the large Atherina boyeri complex and a post-Pleistocene colonisation of the lagoons.  相似文献