磷灰石结构通道离子对晶胞参数的影响   总被引：8，自引：1，他引：8  

刘羽  胥焕岩 《矿物岩石》2001,21(1):1-4

磷灰石晶胞参数受其结构中Ca多面体，磷氧四面体及结构通道位置上的类质同角替换的影响，本文探讨了54个磷灰石样吕的晶胞参数与结构通道离子F，OH，Cl相同象替换的影响，本文讨论了54个磷灰石样品的晶胞参数与结构通道离子F，OH，Cl相对含量的关系，发现Cl和取代是影响岩浆型磷灰石晶胞参数的主要因素，每原子／晶胞的Cl使a增大0．121 1（6）nm，c减少0．0633 （3）nm，根据成分与结构的经验关系式，可以验证电子探针对F的分析结果。  相似文献   

Ground Based FTIR Measurements of Stratospheric Species from Harestua, Norway During Sesame and Comparison with Models     

B. Galle  J. Mellqvist  D.W. Arlander  I. Fløisand  M.P. Chipperfield  A.M. Lee 《Journal of Atmospheric Chemistry》1999,32(1):147-164

Vertical columns of HF, HCl, HNO3, ClONO2, N2O, ClO and COF2 were measured at Harestua, Norway (60.22° N, 10.75° E, Elevation 600 a.s.l.) beginning on 24 November 1994 and concluding on 1 May 1995 during Phase-III of the SESAME (Second European Stratospheric Arctic and Mid-latitude Experiment) measurement campaign. The vertical columns of HCl, HNO3 and ClONO2 measured on 81 days were compared with columns calculated by the 3-D Cambridge model SLIMCAT. In addition the results were also interpreted by comparison with a photochemical trajectory model. Good agreement was seen for HCl while the nitrogen compounds showed larger discrepancies, especially for ClONO2. Evidence for chlorine activation was seen with 65% reduction of the chlorine reservoirs (HCl + ClONO2) while the levels of ClO were greatly enhanced. Interpretation of the loss with the trajectory model indicated condensation of chlorine on PSCs. The vertical column ratio of COF2 and HF was measured to 0.21 outside the vortex and a factor of two lower inside. The recovery of ClONO2 was seen to be much faster than that of HCl in the early spring.  相似文献   

氯化镁及其水合物的标准溶解焓与生成焓     

翟宗玺 《盐湖研究》1993,(1)

利用精密量热仪测定了MgCl_2、MgCl_2·2H_2O、MgCl_2·4H_2O和MgCl_2·6H_2O在298.15°K溶于水的积分溶解热,并利用Pitzer电解质溶液的。~ΦL方程,计算了溶质的相对表观摩尔热焓,从而得到标准溶解焓分别为(KJ·mol~(-1))—155.86±0.17、—79.45±O.17,—41.78±O.18和—14.58±0.16;晶格能分别为—2490.36,—3158.37,—3772.70和—4376.56。二、四、六水合物的标准生成焓分别为—1289.39,—1898.72和—2497.58;水合焓分别为—76.41,—114.08和—141.28。  相似文献   

Porewater geochemistry and solute flux from bottom sediments,Devils Lake,North Dakota   总被引：1，自引：0，他引：1  

Robert M. Lent  W. Berry Lyons 《International Journal of Salt Lake Research》1994,3(2):113-135

Sediment cores were collected for pore-water analysis from the eastern end of Devils Lake, located in northeastern North Dakota, to determine diagenetic reactions occurring in surficial bottom sediments and to evaluate the impact of these reactions on chemical concentrations in the overlying lake water. Sediment pore waters are enriched in major ions and nutrients relative to lake water. The principal sources of major ions to pore water are saline sediments located in the upper 1 m of bottom sediment. The principal source of titration alkalinity and nutrients to pore water is microbial decomposition of sedimentary organic matter by sulfate reduction. Sediment pore waters in the eastern part of Devils Lake have higher major-ion concentrations and solute-flux rates than the sediment pore waters in the central part of the lake. In contrast, sediment pore waters in the central part of Devils Lake have significantly higher nutrient concentrations and solute-flux rates. Major-ion concentrations and solute-flux rates in sediment pore water increase from west to east. These trends indicate that bottom-sediment diagenetic processes are, in part, responsible for the observed concentration gradient in the lake. The higher nutrient concentrations and the higher nutrient diffusional-flux rates in Main Bay are the result of more labile sedimentary organic matter and the occurrence of sulfate reduction. Environmentally-reactive trace-metal concentrations (Cu, Pb, Zn, and Fe) in bottom sediments decrease from west to east with distance from the surface-water sources and with increasing surface-water salinity.  相似文献   

非水溶剂中电解质溶液活度系数的测定:NaCl在1,2-丙二醇中活度系数的测定   总被引：10，自引：3，他引：10       下载免费PDF全文

王卫东  向翠丽  胡珍珠  陆江林 《盐湖研究》2004,12(1):43-45

应用钠离子选择性电极和Ag-AgCl电极组成可逆电池,通过测定电池的电动势,应用Debye H櫣ckel极限公式,计算了不同温度下NaCl在1,2-丙二醇非水溶剂中的活度系数,并根据电解质溶液的溶剂化理论对NaCl的活度系数的某些变化规律进行了讨论。  相似文献   

反浮选-冷结晶法生产氯化钾浮选法除钙研究   总被引：5，自引：1，他引：5       下载免费PDF全文

牛桂然  唐宏学 《盐湖研究》2006,14(1):14-16

研究了青海察尔汗盐湖水采光卤石矿生产氯化钾工艺中浮选除钙的方法。实验结果表明,分级浮选法除钙率平均达88.16%,接近原矿的理论可除钙离子量91.58%。  相似文献   

Major ions characteristics in a disturbed aquifer of an oceanic island——Sipadan, Malaysia     

Mohd Harun Abdullah Baba musta Mazlin Mokhtar Ahmad Zaharin Aris 《中国地球化学学报》2006,25(B08):151-152

The Sipadan island is the only oceanic island found in Malaysia, and is popularly known for its beautiful corals and diving activities. The aquifer of the island is affected by seawater intrusion associated with groundwater exploitation. Geologically, the aquifer is composed of several series of Quaternary bioherm facies, and its recharge merely depends on rainfall. This research attempts to understand the chemical changes of the groundwater attributed to the salinization processes based on major ion composition （Ca^2＋, Mg^2＋, Na^＋, K^＋, HCO, SO, Cl^-）. The initial assessments were done in years 1993 - 1994, followed by subsequent assessment in years 2004-2005. Methods of analyses were adopted from APHA （1995）. The hydrogeochemical saturation indices （SI） were computed using the PHREEQC program in order to assess the state of equilibrium between groundwater and the minerals present. The results of analyses indicated that the groundwater has been highly enriched in Na^＋, SO and CI, reflecting an encroachment of saline water into the aquifer. The groundwater facies can be classified as sodium chloride （Na-Cl） water type. There are positive correlations （moderate to strong）, except HCO3^-, between the studied parameters. The weak and inconsistent correlation of HCO3^- with the cations and anions related to dissolved salts suggests that saltwater intrusion has an insignificant impact on the chemistry of HCO3^- in the groundwater. Strong correlations （r 〉0.70） exist among the major elements （Na^＋, Mg^2＋, K^＋, Cl^- and SO4^-） and salinity （EC）. These relationships clearly identify the main elements contributing to the groundwater salinity and their tendency to depict a similar trend of salinization pattern. Chloride has a major influence on the salinity of groundwater based on the positive and strong correlation that exist between Cl^- and EC （r=0.97）.  相似文献   

氯化钠存在下氯化亚锡-十六烷基三甲基氯化铵体系浮选分离复杂金属基体中锇   总被引：1，自引：0，他引：1  

高云涛 杨宏施润菊  项朋志 《岩矿测试》2006,25(3):246-248

研究了氯化钠存在下氯化亚锡-十六烷基三甲基氯化铵体系对Os（Ⅳ）-三氯锡酸络阴离子的浮选行为。实验表明，在盐酸介质中，体系可以浮选分离Os（Ⅳ），其浮选率为95．2％。98.0％。方法加标回收率为94．0％-98．5％，精密度为2．1％-7．7％（RSD，n=5）。方法可用于从大量基体金属中分离Os（Ⅳ），对实际样品分离的分析结果与其他方法推荐值相符。  相似文献   

Isotopic Composition of Non-Methane Hydrocarbons in Emissions from Biomass Burning     

K. v. Czapiewski  E. Czuba  L. Huang  D. Ernst  A.L. Norman  R. Koppmann  J. Rudolph 《Journal of Atmospheric Chemistry》2002,43(1):45-60

The stable carbon isotope ratios of nonmethane hydrocarbons (NMHC) and methyl chloride emitted from biomass burning were determined by analyzing seven whole air samples collected during different phases of the burning process as part of a laboratory study of wood burning. The average of the stable carbon isotope ratios of emitted alkanes, alkenes and aromatic compounds is identical to that of the burnt fuel; more than 50% of the values are within a range of ±1.5 of thecomposition of the burnt fuel wood. Thus for the majority of NMHC emitted from biomass burning stable carbon isotope ratio of the burnt fuel a good first order approximation for the isotopic composition of the emissions. Of the more than twenty compounds we studied, only methyl chloride and ethyne differed in stable carbon isotope ratios by more than a few per mil from the composition of the fuel. Ethyne is enriched in ¹³C by approximately 20–30, and most of the variability can beexplained by a dependence on flame temperature. The ¹³C values decreaseby 0.019 /K (±0.0053/K) with increasing temperature. Methyl chloride is highly depleted in ¹³C, on average by25. However the results cover a wide range of nearly 30. Specifically, in two measurements with wood from Eucalyptus (Eucalyptus delegatensis) as fuel we observed the emission of extremely light methyl chloride (–68.5and–65.5). This coincides with higher than average emission ratiosfor methyl chloride (15.5 × 10^–5 and 18 ×10^–5 mol CH₃Cl/mol CO₂). These high emission ratios are consistent with the highchlorine content of the burnt fuel, although, due to the limited number of measurements, it would be premature to generalize these findings. The limited number of observations also prevents any conclusion on a systematic dependence between chlorine content of the fuel, emission ratios and stable carbon isotope ratio of methyl chloride emissions. However, our results show that a detailed understanding of the emissions of methyl chloride from chloride rich fuels is important for understanding its global budget. It is also evident that the usefulness of stable carbon isotope ratios to constrain the global budget of methyl chloride will be complicated by the very large variability of the stable carbon isotope ratio of biomass burning emissions. Nevertheless, ultimately the large fractionation may provide additional constraints for the contribution of biomass burning emissions to the atmospheric budget of methyl chloride.  相似文献   

Diagenetic reactions in reservoir strata and geochemical properties of pore fluid and its origin in Songliao Basin     

楼章华  蔡希源等 《中国地球化学学报》1998,17(4):346-355

The reservoirs of the SOngliao Basin are composed of typical unstable sandstones,with high percentages of volcanic fragments and feldspar,In the course of sedimentation and burying,a series of physical and chemical reactions took place between minerals and pore water and water-rock reactions and ion exchange caused changes in ion assemblage of pore water,Hydration-hydrolysis,dissolution and the albitization of feldspar made many ions free from their framework and inter into the pore water,and induced the precipitation of a large amount of authigenic minerals such as smectite and chlorite,During the diagenesis of sandstone.diagenetic reactions involved several stages with increasing depth,and so did the precipitation of authigenic minerals and the transformaiton of minerals.The migration of ions is related with the precipitation,transformation and dissolution of authigenic minerals.Thus,to deepen our study on sandstone diagenesis is an important link for the analysis of ion migration in the evolution of pore water ,the origin and evolution of pore water could be tracked in terms of the geochemistry of fluid inclusions in authigenic minerals.And the isotopic composition of the authigenic mineral calcite can provide its genetic information.  相似文献