黑铜矿、蓝铜矿、孔雀石溶解度图的绘制     

Li Shenghua 《吉林大学学报(地球科学版)》1990,(2)

本文阐述了如何用热力学方法绘制 Cu(Ⅱ)的氧化物、氢氧化物、碳酸盐矿物的溶解度图。  相似文献   

金在表生条件下溶解,迁移和沉淀的探讨   总被引：2，自引：0，他引：2  

周学粹 《矿物岩石》1990,10(3):6-14

金矿物在表生条件下溶解为离子金.离子金与表生络合剂结合成金络离子团迁移.在物化条件改变时,由于有机炭、粘土矿物及带异性电荷胶体吸附,使金络离子团分解成原子金沉淀.  相似文献   

花岗岩中铀性状的实验研究—铀的可溶性及含铀溶液的酸性演化   总被引：3，自引：0，他引：3  

刘正义  姚莲英  仉宝聚 《铀矿地质》1986,(3)

实验主要针对内生条件下花岗岩中铀的可溶性进行的。恒压(500bar)变温(200—400℃,个别达480℃)以及恒温(300℃)变压(100—1500bar)状态下的实验结果表明,花岗岩中铀的最大溶解度多发生在温度低于250℃、压力(P_(H_2O))低于500bar(个别小于1000bar)的范围内。铀最易溶解在碳酸溶液中。伴随压力的降低,碳酸盐和富含碳酸的溶液溶解铀的能力显著增强。含铀溶液随着温度的降低,呈碱性—酸性—碱性演化。  相似文献   

三元体系Na_2B_4O_7-NaHCO_3-H_2O和Na_2CO_3-NaBO_2-H_2O等温溶解度研究     

杨琴  李君  李恒欣  张逢星 《盐湖研究》2001,9(4)

作为研究四元体系Ｎａ２Ｂ４Ｏ７－Ｎａ２ＣＯ３－ＮａＨＣＯ３－ＮａＢＯ２－Ｈ２Ｏ的开端，测定了三元体系Ｎａ２Ｂ４Ｏ７－ＮａＨＣＯ３－Ｈ２Ｏ和Ｎａ２ＣＯ３－ＮａＢＯＨ２－Ｈ２Ｏ在０℃、１５℃－４５℃时的溶解度，绘制了相应的组成－性质图。两个三元体系的溶度图在研究温度范围内均属于低共饱型，平衡固相为组分化合物或其水合物。  相似文献   

硫化物矿物溶解度与溶液pH值的关系   总被引：2，自引：0，他引：2  

贾建业  兰斌明  谢先德  吴大清  汤艳杰  王燕  王建成 《吉林大学学报(地球科学版)》2001,31(3):241-246

硫化物作为自然界常见的一大类矿物 ,由于溶解度很小 ,硫化物对水pH值的影响以及水对它的溶解度影响往往被人们所忽视。通过计算常见硫化物矿物的自由能ΔG0f、溶度积Ksp和溶解度S、绘制logS—pH曲线 ,得出硫化物矿物在不同 pH值条件下的溶解规律 ,水溶液的pH值受硫化物矿物的控制 ;反过来 ,水溶液的pH值也影响着矿物溶解度的大小。此外 ,对硫化物矿物饱和溶液的缓冲范围、缓冲容量和硫化物与溶液pH值相互作用的机理进行了探讨  相似文献   

Water-soluble organics in atmospheric particles: A critical review of the literature and application of thermodynamics to identify candidate compounds   总被引：15，自引：0，他引：15  

Pradeep Saxena  Lynn M. Hildemann 《Journal of Atmospheric Chemistry》1996,24(1):57-109

Although organic compounds typically constitute a substantial fraction of the fine particulate matter (PM) in the atmosphere, their molecular composition remains poorly characterized. This is largely because atmospheric particles contain a myriad of diverse organic compounds, not all of which extract in a single solvent or elute through a gas chromatograph; therefore, a substantial portion typically remains unanalyzed. Most often the chemical analysis is performed on a fraction that extracts in organic solvents such as benzene, ether or hexane; consequently, information on the molecular composition of the water-soluble fraction is particularly sparse and incomplete.This paper investigates theoretically the characteristics of the water-soluble fraction by splicing together various strands of information from the literature. We identify specific compounds that are likely to contribute to the water-soluble fraction by juxtaposing observations regarding the extraction characteristics and the molecular composition of atmospheric particulate organics with compound-specific solubility and condensibility for a wide variety of organics. The results show that water-soluble organics, which constitute a substantial fraction of the total organic mass, include C2 to C7 multifunctional compounds (e.g., diacids, polyols, amino acids). The importance of diacids is already recognized; our results provide an impetus for new experiments to establish the atmospheric concentrations and sources of polyols, amino acids and other oxygenated multifunctional compounds.  相似文献   

豫西南矽线石物相分析方法研究   总被引：2，自引：2，他引：2  

程广才  阮福增 《岩矿测试》1993,12(1):50-53

以豫西南地区4个矿区的矿物组合为依据,建立了铝量法测定矽线石含量的物相分析方法。对比了不同方法制备的矽线石及其不同存在条件下溶解率的差异,确定了接近矿区实际的、准确合理的分析结果校正办法。  相似文献   

天然气水合物体系的相平衡及甲烷溶解度计算          下载免费PDF全文

苏正  陈多福  冯东  刘芊 《地球物理学进展》2007,22(1):239-246

海洋环境中天然气水合物的形成除了合适的温压条件外，还必须有充分的甲烷供给.本文介绍了甲烷-水体系的甲烷饱和溶解度、水合物体系中甲烷水合物溶解度计算方法.在气-液二相平衡甲烷饱和溶解度计算中，关键在于状态方程的选择和合适的混合规则的运用，Duan的计算模型在温度、压力和盐度变化上都具有很大的适用性，且易于应用.在含水合物的相平衡体系中，在已知组分和假定可能存在相的前提下，可利用模拟退火算法优化总吉布斯自由能，确定是二相还是三相体系，并求解甲烷水合物溶解度.在海水环境下盐的存在使平衡发生移动，利用德拜—休克尔理论或Pitzer电解质溶液理论校正盐度对于海水活度的影响，求解海水环境中甲烷水合物溶解度.基于气-液二相平衡理论的K-K方程，在临近水合物生成条件下实验或计算确定亨利常数等参数后，可计算三相平衡甲烷水合物溶解度，且简单易用.  相似文献   

On the quantitative evaluation of metamorphic fluid composition: Verification of the results of physicochemical simulations for water-mineral-rock reactions     

V. O. Khudolozhkin 《Russian Journal of Pacific Geology》2007,1(3):290-301

This paper reports the results of a comparison of the qualitative physicochemical simulations (by the Winsel program complex) of the composition of the reacting fluid with experimental data on the water-electrolyte (NaCl, HCl, NaOH, and KOH)-mineral (quartz, corundum, microcline, and plagioclase) system and the water-electrolyte-rock (granite and pelite) system at 400–800°C and 1–10 kbar. Constraints are proposed for the temperature, pressure, and the composition of the electrolyte at which the simulation results are consistent with the experimental data.  相似文献   

The Henry's Law Constants of the Haloacetic Acids     

D. J. Bowden  S. L. Clegg  P. Brimblecombe 《Journal of Atmospheric Chemistry》1998,29(1):85-107

Henry's law constants K_H (mol kg^-1 atm^-1) have been measured between 278.15 K and 308.15 K for the following organic acids: CH₂FCOOH (ln(K_H[298.15 K]) = 11.3 ± 0.2), CH₂ClCOOH (11.59 ± 0.14), CH₂BrCOOH (11.94 ± 0.21), CHF₂COOH (10.32 ± 0.10), CHCl₂COOH (11.69 ± 0.11), CHBr₂COOH (12.33 ± 0.29), CBr₃COOH (12.61 ± 0.21), and CClF₂COOH (10.11 ± 0.12). The variation of K_H with temperature was determined for all acids except CH₂FCOOH and CBr₃COOH, with _r H° for the dissolution reaction ranging from –85.2 ± 2.6 to –57.1 ± 2.5 kJ mol^-1, meaning that their solubility is generally more sensitive to temperature than is the case for the simple carboxylic acids. The Henry's law constants show consistent trends with halogen substitution and, together with their high solubility compared to the parent (acetic) acid (ln(K_H[298.15 K]) = 8.61), present a severe test of current predictive models based upon molecular structure. The solubility of haloacetic acids and strong dissociation at normal pH mean that they will partition almost entirely into cloud and fog in the atmosphere (0.05–1.0 g H₂O m^-3), but can reside in both phases for the liquid water contents typical of aerosols (10^-5-10^-4 g H₂O m^-3).  相似文献