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IntroductionThe Zhabuye salt lake, Tibet in China, is famousfor the high concentrations of lithium, boron, andpotassium in the world. The main components areLi , K , Na , B4O72 -, CO32 -, Cl-, SO42 -, andH2O, including rare elements such as Rb and Cs .The…  相似文献   

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According to the compositions of the underground gasfield brines in the west of Sichuan Basin, the solu- bilities and densities of the solid-liquid equilibria in the quaternary system Na+, K+//Br-, B4O72--H2O at 298 K were determined by the method of isothermal solution saturation. From the experimental data, the phase diagram, water content diagram and density-composition diagram were obtained. This quaternary system is of simple eutectic type, without double salt and solid solution. There are two invariant points, five univariant curves, four fields of crystalli- zation in the system. The equilibrium solid phases are Na2BaO7·10H20, K2B4O7·4H2O, NaBr·2H2O and KBr. Na2B4O7·10H2O has a larger crystallization field, and NaBr·2H2O has a smaller crystallization field. It is also found that bromide has the salting-out effect on borate in the quaternary system Na+, K+//Br-, B4O72--H2Oat 298 K.  相似文献   

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得到Na^ ,K^ ,Mg^2 ∥Cl^-,SO4^2--H2O五元体系15℃时的介稳溶解度数据,绘制了该体系在15℃的介稳相图,共有9个为氯化钠所饱和结晶区域:氯化钾,硫酸钠,钾钠芒硝,软钾镁矾,白钠镁矾,光卤石,七水硫酸镁,六水硫酸镁和水氯镁石。所得15℃介稳相图和Van‘t Hoff稳定相图比较有较大区别;在15℃介稳相图中钾镁矾,钾盐镁矾以及五水硫酸镁和四水硫酸镁结晶区域消失,而软钾镁矾结晶区域显著扩大。比较作者所作该五元体系15℃,25℃及35℃介2稳相图,发现软钾镁矾(包括钾镁矾)相区以25℃时最大,35℃时最小,随温度升高,钾钠芒硝结晶相区依次向KCl相区平行移动,导致KCl相区缩小,Na2SO4相区扩大,随温度升高相应点的钠含量和水含量依次减小。  相似文献   

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Phase equilibria of the quaternary NaCl–NaBr–Na2SO4–H2O system at 323 K were studied by the isothermal dissolution equilibrium method. The solubilities of salts and densities of saturated solutions were determined. Solid solutions [Na(Cl, Br)] were found in the experiments. The phase diagram of the quaternary system has no invariant point, but has one univariant curve at the boundary of Na(Cl, Br) and Na2SO4 crystallization fields. The experimental results show that an increase of the NaBr concentration is accompanied by an obvious increase of the solution density and the decrease of the solubilities of NaCl and Na2SO4.  相似文献   

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得到Na+, K+, Mg2+∥Cl-, SO2-4-H2O五元体系15 ℃时的介稳溶解度数据, 绘制了该体系15 ℃的介稳相图, 共有9个为氯化钠所饱和的结晶区域 氯化钾、硫酸钠、钾钠芒硝、软钾镁矾、白钠镁矾、光卤石、七水硫酸镁、六水硫酸镁和水氯镁石. 所得15 ℃介稳相图和Vant Hoff稳定相图比较有较大区别; 在15 ℃介稳相图中钾镁矾、钾盐镁矾以及五水硫酸镁和四水硫酸镁结晶区域消失, 而软钾镁矾结晶区域显著扩大. 比较作者所作该五元体系15 ℃, 25 ℃及35 ℃介稳相图, 发现软钾镁矾(包括钾镁矾)相区以25 ℃时最大, 35 ℃时最小; 随温度升高, 钾钠芒硝结晶相区依次向KCl相区平行移动, 导致KCl相区缩小, Na2SO4相区扩大; 随温度升高相应点的钠含量和水含量依次减小.  相似文献   

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Na+, K+, Mg2+∥Cl-, SO2-4-H2O五元体系35 ℃介稳相图研究   总被引:3,自引:0,他引:3  
研究得出(Na+, K+, Mg2+∥Cl-, SO2-4-H2O)五元体系35 ℃时的介稳溶解度数据,绘制了该体系35 ℃的介稳相图,共有9个为氯化钠所饱和的结晶区域:氯化钾、钾芒硝(3K2SO4*Na2SO4)、钾镁矾(K2SO4*MgSO4*4H2O)、钾盐镁矾(KCl*MgSO4*2.75H2O)、光卤石(KCl*MgCl2*6H2O)、白钠镁矾(Na2SO4*MgSO4*4H2O)、硫酸钠、六水硫酸镁(MgSO4*6H2O)和水氯镁石(MgCl2*6H2O). 所得35 ℃介稳相图与Vant Hoff 25 ℃稳定相图比较有较大区别:软钾镁矾(K2SO4*MgSO4*6H2O)、七水硫酸镁、五水硫酸镁及四水硫酸镁结晶区域消失,钾镁矾和钾盐镁矾结晶区域显著扩大. 所得35 ℃介稳相图与25 ℃介稳相图区别很大:软钾镁矾和七水硫酸镁结晶区域消失,同时出现了钾镁矾和钾盐镁矾的结晶区域. 在该五元体系35 ℃介稳相平衡研究中发现析出的是钾盐镁矾的低水化合物(KCl*MgSO4*2.75H2O).  相似文献   

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Metastable equilibrium solubilities and densities of quaternary system Li2SO4+Li2CO3+ Li2B4O7+H2O at 288 K were determined by isothermal evaporation method. According to the experimental data, the metastable equilibrium phase diagram was plotted. The metastable phase diagram had one invariant point F, three double saturated liquid curves E1F, E2F and E3F, and three crystallization fields corresponding to Li2SO4·H2O, Li2CO3 and LiBO2·8H2O. It was found that lithium sulphate(Li2SO4) had the highest concentrat...  相似文献   

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采用等温蒸发法研究了四元体系Na+, K+//Cl-, B4O2-7-H2O 273 K时的介稳相平衡与相图. 测定了该体系273 K平衡液相中各组分的溶解度及平衡液相的密度; 绘制了该体系的介稳相图. 该四元体系273 K相图由5条溶解度单变量线、4个结晶区及2个共饱和点组成. 体系无复盐或固溶体形成. 四个结晶区分别对应单盐NaCl、KCl、K2B4O7·4H2O 和Na2B4O7·10H2O. 共饱点E1处KCl、NaCl及Na2B4O7·10H2O三盐共饱和,所对应的平衡液相组成为w(Cl-)=29.15%, w(B4O2-7)=0.64%, w(K+)=5.97%, w(Na+)=15.55%; 共饱和点E2处盐KCl、Na2B4O7·10H2O和K2B4O7·4H2O的三盐共饱和, 所对应的平衡液相组成为w(Cl-)=22.84%, w(B4O2-7)=10.98%, w(K+)=28.01%, w(Na+)=1.53%. 同体系298 K时的稳定相图相比, 273 K时硼酸钠的结晶区变大, 而硼酸钾、氯化钠结晶区变小.  相似文献   

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采用等温蒸发法研究了四元体系Na2CO3-Na2SO4-Na2B4O7-H2O在273 K时的介稳相平衡及平衡液相的密度. 利用溶解度数据绘制了该四元体系273 K下的相图. 研究结果表明, 该四元体系有异成分复盐2Na2SO4·Na2CO3形成. 相图中有2个共饱点、5条单变量曲线和4个结晶相区. 4个结晶相区分别为盐Na2CO3·10H2O, Na2SO4·10H2O, Na2B4O7·10H2O和2Na2SO4·Na2CO3的结晶区. 复盐2Na2SO4·Na2CO3同时存在于包含Na2CO3-Na2SO4-H2O三元体系的其它四元体系或高元体系中. 在273 K介稳平衡相图中, 碳酸钠以Na2CO3·10H2O形式析出; 硫酸钠以Na2SO4·10H2O的形式析出; 硼酸钠的完整分子式为Na2B4O5(OH)4·8H2O. Na2CO3对Na2B4O7有盐析作用.  相似文献   

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The component solubilities, densities and refractive indices of the quaternary system Na+, Rb+, Mg2+//Cl--H2O at 298.2 K were measured using an isothermal evaporation method. Based on the gathered data, a metastable phase diagram, a water content diagram, and a density/refractive index vs. composition diagram were constructed. The results show that this system is of a complex type with a double salt rubidium carnallite (RbCl·MgCl2·6H2O) formed at 298.2 K. Double salt rubidium carnallite, whose component point locates in its own crystallization zone in the dry salt phase diagram, belongs to congruent double salt at 298.2 K. Accompanied by the double salt that was formed, there are two invariant points in the phase diagram that cosaturated with three salts and an equilibrated solution. The cosaturated salts for the two invariant points are MgCl2·6H2O+RbCl·MgCl2·6H2O+ NaCl and NaCl+RbCl+RbCl·MgCl2·6H2O, respectively. Both invariant points are commensurate invariant points in the evaporation process, and the two invariant points are evaporative dry points. The sizes of the crystalline regions of the salts are in the order of NaCl > RbCl > RbCl·MgCl2·6H2O > MgCl2·6H2O.  相似文献   

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采用等温蒸发平衡法研究了四元体系K2B4O7-Na2B4O7-Li2B4O7-H2O在273 K时的介稳相平衡及平衡液相的密度. 研究发现该四元体系为简单共饱和型, 无复盐及固溶体形成, 根据溶解度数据绘制了相图, 相图中有一个共饱点E, 三条单变度曲线E3E, E2E, E1E; 三个平衡固相分别为K2B4O7·4H2O、Na2B4O7·10H2O 和LiBO2·8H2O. 并简要讨论了实验结果.  相似文献   

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(Solid+Liquid) phase equilibria in the quaternary system Na2B4O7‐MgB4O7‐K2B4O7‐H2O at 288 K were studied experimentally using the method of isothermal solution saturation. Solubility of any single salt in the solution of the quaternary system was determined experimentally. Based on the experimental data achieved, the phase diagram and water content diagram of the quaternary system were constructed, respectively. In the phase equilibrium diagram of the quaternary system Na2B4O7‐MgB4O7‐K2B4O7‐H2O at 288 K, there are one invariant point E, three univariant curves E1E, E2E and E3E, and three fields of crystallization corresponding to Na2B4O7·10H2O, K2B4O7·4H2O and MgB4O7·9H2O. The experimental results show that potassium borate (K2B4O7·4H2O) have higher solubilities than the magnesium borate and sodium borate in the quaternary system Na2B4O7‐MgB4O7‐K2B4O7‐H2O at 288 K.  相似文献   

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Solid-liquid equilibrium of quaternary system Cd2+//Cl-, SO42-, NO3--H2O at 298 K was studied by means of an isothermal solution saturation method. Experimental results indicate that there are three univariant curves BE, AE and CE, one invariant point E and three crystallization fields in the quaternary system. The quaternary system belongs to a simple type, and there are no double salts or solid solution existing. The crystallization zones of equilibrium solid phases are CdCl2·5/2H2O(AEB field), 3CdSO4·8H2...  相似文献   

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The metastable solubilities and the physicochemical properties including density and pH of the reciprocal quaternary system(LiCl+MgCl2+Li2SO4+MgSO4+H2O) at 348.15 K and 0.1 MPa were determined using the isothermal evaporation method. The dry-salt diagram and water-phase diagram were plotted based on the experimental data. There are five invariant points, eleven univariant curves, and seven crystallization zones corresponding to hexahydrite, tetrahydrite, kieserite, bischofite, lithium sulfate monohydrate, lithium chloride monohydrate and lithium carnallite. Comparison between the stable and metastable diagrams at 348.15 K indicates that the metastable phenomenon of magnesium sulfate is obvious, and the crystallization regions of hexahydrite and tetrahydrite disappear in the stable phase diagram. A comparison of the metastable dry-salt phase diagrams at 308.15, 323.15 and 348.15 K shows that with the increasing of temperature the epsomite crystallization zone disappears from the dry-salt phase diagram of 303.15 K, and a new kieserite crystallization zone is presented at 348.15 K. The density and pH in the metastable equilibrium solution present regular change with the increasing of Jänecke index J(2Li+), and the calculated densities using the empirical equation agree well with the experimental values.  相似文献   

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我国青藏高原由于特殊的地理气候特点而盐湖众多,西藏境内的扎布耶盐湖卤水中锂、硼、钾浓度之高,在世界盐湖中也非常罕见[1-3].  相似文献   

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Solid-liquid phase equilibria of the two ternary systems (NaCl+SrCl2+H2O) and (KCl+SrCl2+H2O) at T=288.15 K and p=0.1 MPa were studied using the isothermal dissolution equilibrium method. Solubilities of the equilibrium liquid phase were determined, and the solids were also investigated by the Schreinemaker method of wet residues. In the ternary system (NaCl+SrCl2+H2O) at 288.15 K, there is one invariant point corresponding to (NaCl+SrCl2·6H2O) and two crystallization regions corresponding to NaCl and SrCl2·6H2O. The crystallized area of SrCl2·6H2O decreased with the increasing temperature, while that of NaCl increased slightly. In the ternary system (KCl+SrCl2+H2O) at 288.15 K, there is one invariant point(KCl+SrCl2·6H2O) and two crystallization regions corresponding to KCl and SrCl2·6H2O. Both systems belong to a simple eutectic type, and neither double salts nor solid solutions were formed. On the basis of Pitzer-Harvie-Weare model, the solubilities of the two systems at 288.15 K were demonstrated. A comparison showed that the calculated solubilities agreed well with the experimental data.  相似文献   

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