研究地球化学机制的热动力学方法

章介绍了热动力学方法的研究历史，研究原理以及在研究地球化学机制中的应用，如石膏的脱水反应机制可分二步进行，ＣａＳｏ４．２Ｈ２Ｏ→ＣａＳＯ４．１／２Ｈ２Ｏ→ＣＳＯ４活化能Ｅ＝１１８．７ＫＪ／ｍｏｌ，脱水温度Ｔ＝３８０．６０，呱应速率Ｋ１＝４．４１×１０＾－４Ｓ＾－１方解石的溶解反应机制，在０－５０００Ｓ期间以溶解反应为主，嗣后，发生周期性的溶解反应，热谱图上表现为化学振荡。     

金川铜镍硫化矿床成矿温度压力计算及成矿机制探讨

本文利用橄榄石温度计、压力计的方法,计算金川超基性岩体主要含矿岩相成岩的温度压力条件。根据计算所得的温压数据、矿石结构特征、含矿岩相的相互接触关系及储量分布,判断矿床成因主要属于深部熔集型,并根据不可逆过程热力学平衡扩散方程,探讨硫化物(Ni~(2+),S~(2-))和硅酸盐熔浆(Si_4~(4-))产生熔集的机制。     

非平衡热力学在短期灾害性天气预报中的应用

综述了非平衡热力学应用于天气预报的若干进程以及在短期灾害性天气预报应用中的明显效果。     

C—O—H体系高温高压流体相组成的热力学研究

本文在C－O－H体系流体相平衡基础上,利用现有的热力学数据和新的p－V－T资料,在pT=∑pi假定下,计算了高温、高压条件下流体相组成。结果表明,该体系主要存在五种流体相,在不同温压条件下各流体相所占比例不同。在相对较低的温、压条件下,CH4是体系中占主要的流体相（约占70％）,且随温、压和氧逸度的升高,它所占比例却明显降低,所获结果为探讨无机成因天然气形成的可能性、存在的量比和稳定存在的物理化学条件提供了充分的理论依据。     

地形对降水的影响研究概述

简要回顾了近些年来有关地形对降水影响的研究进展。介绍了地形的动力效应和热力效应,详细分析了地形的动力、热力效应引起的降水和云物理变化。重点分析了地形对气候尺度、天气尺度、中尺度及对流性天气系统降水的影响。简单地讨论了在研究地形对降水影响时观测分析、气候统计、理论分析及数值模拟方面存在的问题及其未来发展前景。     

Studies on the Thermodynamics and Thermal Chemistry Properties for Lithium Salts and Their Aqueous Solution Systems

正1 Introduction With the industrial development of lithium battery,nuclear and aerospace industry,the demands of metal lithium and its compounds are increasing significantly.Lithium is called as the energy of the metal in the new century(Zhang et al.2001).The total reserve of lithium resources around the world7     

Gravitational clustering of galaxies in an expanding universe

We inquire the phenomena of clustering of galaxies in an expanding universe from a theoretical point of view on the basis of thermodynamics and correlation functions. The partial differential equation is developed both for the point mass and extended mass structures of a two-point correlation function by using thermodynamic equations in combination with the equation of state taking gravitational interaction between particles into consideration. The unique solution physically satisfies a set of boundary conditions for correlated systems and provides a new insight into the gravitational clustering problem.     

The Solubility of Sulphur in Hydrous Rhyolitic Melts

Experiments performed at 2 kbar, in the temperature range 800–1000°C,with fO₂ between NNO–2·3 and NNO+2·9 (whereNNO is the nickel–nickel oxide buffer), and varying amountsof sulphur added to hydrous metaluminous rhyolite bulk compositions,were used to constrain the solubility of sulphur in rhyolitemelts. The results show that fS₂ exerts a dominant control onthe sulphur solubility in hydrous silicate melts and that, dependingon fO₂, a rhyolitic melt can reach sulphur contents close to1000 ppm at high fS₂. At fO₂ below NNO+1, the addition of ironto a sulphur-bearing rhyolite magma produces massive crystallizationof pyrrhotite and does not enhance the sulphur solubility ofthe melt. For a given fO₂, the melt-sulphur-content increaseswith fS₂. For fixed fO₂ and fS₂, temperature exerts a positivecontrol on sulphur solubilities, at least for fO₂ below NNO+1.The mole fraction of dissolved sulphur exhibits essentiallylinear dependence on fH₂S at low fO₂ and, although the experimentalevidence is less clear, on fSO₂ at high fO₂. The minimum insulphur solubility corresponds to the redox range where bothfH₂S and fSO₂ are approximately equal. A thermodynamic modelof sulphur solubility in hydrous rhyolite melts is derived assumingthat total dissolved sulphur results from the additive effectsof H₂S and SO₂ dissolution reactions. The model reproduces wellthe minimum of sulphur solubility at around NNO+1, in additionto the variation of the sulphide to sulphate ratio with fO₂.A simple empirical model of sulphur solubility in rhyoliticmelts is derived, and shows good correspondence between modeland observations for high-silica rhyolites. KEY WORDS: sulphur; solubility; rhyolite; thermodynamics; fO₂; fS₂     

The mechanisms of paragenesis and separation of silver, lead and zinc in hydrothermal solutions

On the basis of an experimental study and thermodynamic calculation, the mechanisms of paragenesis and separation of silver, lead and zinc in the hydrothermal system have been studied. At acidic to nearly neutral pH, their chloride complexes are stable, and among them the chloride complexes of zinc are most stable. And the sulfide complexes are the dominant species at nearly neutral to alkaline pH,while the sulfide complexes of silver are most stable. With decreasing temperature, [ Cl^-] ,fO2, and increasing pH, the solubilities of silver, lead and zinc will decrease, leading to their deposition and separation. For sulfide complexes, the concentrations of reduced sulfur and pH are two important factors affecting their stabilities. Complexes of different forms and stabilities respond to the variation of conditions to different extents, which gave rise to the paragenesis and separation of silver, lead and zinc in the whole ore-forming process of dissolution, transport and deposition.     

Energy and first law of thermodynamics for Born—Infeld—anti-de-Sitter black hole

We calculate the local energy and the energy density of the Reisner--Norstrõm--anti-de-Sitter black hole, study the first law of thermodynamics and show the Smarr formula for the Born--Infeld--anti-de-Sitter black hole. Applying the first law of thermodynamics to the black hole region, we analyse the three energy exchange processes between the black hole region and the outer and the inner regions.