四元体系(LiCl + NaCl + Li2SO4 + Na2SO4 + H2O)在75℃等温蒸发相平衡实验与理论研究

梯度太阳能池技术在盐湖化工中是一种经济分离无机盐产品的方法,本文创新性的采用等温蒸发法,模拟四元体系(LiCl + NaCl + Li2SO4 + Na2SO4 + H2O)在75℃等温蒸发相平衡,指导太阳池深池积温分离提取锂盐产品。实验测定了溶解度和溶液密度、pH值等物化性质,并绘制了干盐相图、水图和物化性质组成图。在该四元体系干盐相图中包含3个四元共饱点,7条单变量蒸发曲线和5个结晶区,分别为NaCl,Na2SO4,复盐Li2SO4·Na2SO4,Li2SO4·H2O和LiCl·H2O。采用 Pitzer模型和改进的HMW公式,拟合出该四元体系在75℃时的Pitzer单盐参数、混合离子作用参数和平衡固相的热力学平衡常数,并计算给该四元体系的相图,计算相图和实验相图有较大区别。等温蒸发相图能真实的反应盐湖中盐类沉积规律,并对指导太阳池分离盐类具有重要指导意义。     

氯盐和冻融耦合下水泥土的强度和破坏特征

为了研究氯盐侵蚀和冻融循环耦合下水泥土无侧限抗压强度和破坏特征, 进行了不同浓度氯化钠溶液下的水泥土冻融循环试验, 得到了冻融前后的冻融腐蚀因子、 体积变化率和变形模量, 分析了微观结构特征。结果表明： 在氯盐侵蚀和冻融循环耦合下, 水泥土的无侧限抗压强度、 冻融腐蚀因子均随着冻融循环次数的增加而呈现下降趋势; 氯盐浓度越高, 水泥土的无侧限抗压强度、 冻融腐蚀因子下降的幅度越大。随着冻融循环次数的增加, 在同种浓度溶液中, 水泥土的体积变化率增大, 变形模量减小; 氯盐浓度增大, 水泥土体积膨胀变大, 内部结构松散, 抵抗变形的能力减弱。相同冻融循环次数下, 氯盐溶液产生的损伤要大于清水中的损伤, 随着氯盐溶液浓度的增加, 水泥土内部微观结构损伤越严重。     

氯化钾诱导中华绒螯蟹三倍体参数的优化

基于受精卵早期发育形态学的观察,对利用氯化钾诱导中华绒螯蟹(Eriocheir sinensis)三倍体的条件进行了优化.实验结果表明:中华绒螯蟹受精卵在产出后经历了变圆、体积膨大及卵黄团物质位置移动的过程;在15℃下,中华绒螯蟹受精卵在产出后40 min左右释放第一极体,80 min左右孵化膜形成并举起,5 h左右第二极体释放;氯化钾诱导中华绒螯蟹三倍体的优化参数为:产卵后1.5～2.0 h,用6 g/L的氯化钾处理4 h;孵化膜形成并举起可以作为中华绒螯蟹三倍体诱导开始点的形态学标记,其最高诱导率可以达到100%.实验结果为实现中华绒螯蟹三倍体苗种的批量生产提供了参考和依据.     

不同盐度下鲈鱼稚鱼鳃的显微结构观察

采用石蜡切片和显微摄影技术,研究了不同盐度下鲈鱼(Lateolabrax japonicus)稚鱼鳃的显微结构.结果显示,在15.00盐度组,稚鱼鳃的鳃丝和鳃小片上泌氯细胞数量较多,泌氯细胞集中分布在鳃小片基部,且黏液细胞较多.与15.00盐度组和淡水组相比,7.50盐度组稚鱼鳃的鳃小片较窄,泌氯细胞的分布、结构及数量变化均不明显.在0.00盐度组,稚鱼鳃中鳃小片较宽,排列紧密,泌氯细胞数量较少,且主要分布在近鳃小片基部.鲈鱼稚鱼鳃的结构能够适应外界水体盐度的变化,其中泌氯细胞的结构和数量变化是与鲈鱼稚鱼所处的环境相适应的.     

氯化物型盐碱地池塘水化学特征的研究

1997年4月～1998年4月对位于黄河下游氯化物型盐碱地池塘的水化学进行了周年分析。结果表明(1)该类水体的水型基本为 Cl     

EVOLVING FACTOR ANALYSIS APPLIED TO FLOW INJECTION ANALYSIS DATA

Evolving factor analysis is used to estimate the concentration profiles and spectra of Bi~(3 )and the bismuthchloride complexes BiCl~(2 )through BiCl_6~(3-)formed by injection of bismuth percblorate into a flowingstream of 1.0 mol l~(-1) HCl.The estimated spectra compare favorably with previously published spectraof the complexes.     

Groundwater recharge in the Akaki catchment,central Ethiopia: evidence from environmental isotopes (δ18O, δ2H and 3H) and chloride mass balance

Recharge patterns, possible flow paths and the relative age of groundwater in the Akaki catchment in central Ethiopia have been investigated using stable environmental isotopes δ¹⁸O and δ²H and radioactive tritium (³H) coupled with conservative chloride measurements. Stable isotopic signatures are encoded in the groundwater solely from summer rainfall. Thus, groundwater recharge occurs predominantly in the summer months from late June to early September during the major Ethiopian rainy season. Winter recharge is lost through high evaporation–evapotranspiration within the unsaturated zone after relatively long dry periods of high accumulated soil moisture deficits. Chloride mass balance coupled with the isotope results demonstrates the presence of both preferential and piston flow groundwater recharge mechanisms. The stable and radioactive isotope measurements further revealed that groundwater in the Akaki catchment is found to be compartmentalized into zones. Groundwater mixing following the flow paths and topography is complicated by the lithologic complexity. An uncommon, highly depleted stable isotope and zero‐³H groundwater, observed in a nearly east–west stretch through the central sector of the catchment, is coincident with the Filwoha Fault zone. Here, deep circulating meteoric water has lost its isotopic content through exchange reactions with CO₂ originating at deeper sources or it has been recharged with precipitation from a different rainfall regime with a depleted isotopic content. Copyright © 2006 John Wiley & Sons, Ltd.     

铅电解原料工业硅氟酸中硫酸根的快速测定

用硝酸钾溶液沉淀硅氟酸根离子，分离大量的基体，滤液与氯化钡在保护剂的作用下，形成硫酸钡悬浊液，用分光光度计于波长440nm处测定其吸光度。方法的表观摩尔吸光系数为1.7×10^5L·mol^-1·cm^-1，测定范围为0、04～0．48g／L。应用于铅电解原料工业硅氟酸中硫酸根的测定，结果与重量法基本一致，7次测定的相对标准偏差小于7％，加标回收率为97．5％～101．7％。     

氯盐溶液的拉曼光谱特征及测试探讨

常温下氯盐溶液水的拉曼包络线歪斜度受氯离子浓度和阳离子的影响,水拉曼包络线歪斜度很难准确评价复杂流体中的氯离子浓度,在-170℃下氯盐溶液的拉曼光谱研究表明,H2O和nCl-[H OH-]n的拉曼光谱峰能很好地分解并明显地显示,其中nCl-[H OH-]n的拉曼峰与H2O的拉曼峰比值与氯盐的浓度呈正相关,用nCl-[H OH-]n的拉曼特征峰强度(I3401～3413.18cm-1)与H2O的拉曼特征峰强度(I3088～3106cm-1)比值(InCl-[H -OH-]n/IH2O)为纵座标,作相关图,二者的相关性较好,可以应用于溶液中氯离子摩尔浓度测定。     

Chemical evolution and volcanic activity of the active crater lake of Poás volcano, Costa Rica, 1993–1997

Concentrations of chloride and sulfate and pH in the hot crater lake (Laguna Caliente) at Poás volcano and in acid rain varied over the period 1993–1997. These parameters are related to changes in lake volume and temperature, and changes in summit seismicity and fumarole activity beneath the active crater. During this period, lake level increased from near zero to its highest level since 1953, lake temperature declined from a maximum value of 70°C to a minimum value of 25°C, and pH of the lake water increased from near zero to 1.8. In May 1993 when the lake was nearly dry, chloride and sulfate concentrations in the lake water reached 85,400 and 91,000 mg l⁻¹, respectively. Minimum concentrations of chloride and sulfate after the lake refilled to its maximum volume were 2630 and 4060 mg l⁻¹, respectively. Between January 1993 and May 1995, most fumarolic activity was focused through the bottom of the lake. After May 1995, fumarolic discharge through the bottom of the lake declined and reappeared outside the lake within the main crater area. The appearance of new fumaroles on the composite pyroclastic cone coincided with a dramatic decrease in type B seismicity after January 1996. Between May 1995 and December 1997, enhanced periods of type A seismicity and episodes of harmonic tremor were associated with an increase in the number of fumaroles and the intensity of degassing on the composite pyroclastic cone adjacent to the crater lake. Increases in summit seismic activity (type A, B and harmonic tremor) and in the height of eruption plumes through the lake bottom are associated with a period of enhanced volcanic activity during April–September 1994. At this time, visual observations and remote fumarole temperature measurements suggest an increase in the flux of heat and gases discharged through the bottom of the crater lake, possibly related to renewed magma ascent beneath the active crater. A similar period of enhanced seismic activity that occurred between August 1995 and January 1996, apparently caused fracturing of sealed fumarole conduits beneath the composite pyroclastic cone allowing the focus of fumarolic degassing to migrate from beneath the lake back to the 1953–1955 cone. Changes in the chemistry of summit acid rain are correlated changes in volcanic activity regardless of whether fumaroles are discharging into the lake or are discharging directly into the atmosphere.