灼烧处理对纤蛇纹石反应活性的影响

    使用可循环的NH4Cl 溶液作为中间媒介获取Mg2+用于CO2 矿物封存是一种新兴工艺,但是纤蛇纹石在NH4Cl 溶液中较 低的Mg2+浸出率却是这项工艺发展的瓶颈。针对这一问题,本文采用灼烧处理对纤蛇纹石进行改性。结果表明, 灼烧处理 可以有效改变纤蛇纹石中Mg2+反应活性。在600℃灼烧后,所得产物与NH4Cl 反应的转化率达到55.64%,比灼烧前提高了 约43%。600℃灼烧处理脱除了纤蛇纹石外羟基,增大了矿物的反应表面积和具反应活性的Mg2+的量,促进了其与NH4Cl 的 反应 ;脱除内羟基后,具反应活性Mg2+减少,与NH4Cl 反应的转化率降低。     

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。     

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.     

白云石半焙烧物中游离氧化钙的测定

介绍了一种测定白云石半焙烧产物中游离氧化钙的方法,采用氯化镁溶液将氧化钙浸取为可溶性钙盐,进而用EDTA标准溶液滴定。该方法不同于传统的测定方法,其操作简单,分析快速,测定准确时间短,结果重现性好,适合白云石焙烧控制分析。     

Microstructure of NH4Cl-NH3-H2O system studied by ATR-FTIR, Raman and MD simulation

The solubilities of ammonium chloride in aqueous ammonia decreased first and then increased with increasing ammonia concentrations, but the mechanism of this phenomenon has not been clarified. In the present work, the ATR-FTIR and Raman spectroscopy were employed to investigate the corresponding mechanism. The spectra analysis was focused on the region between 2500 and 4000 cm-1. It was firstly discovered that the N-H???N hydrogen bonds between ammonium ions and ammonia molecule was mainly formed in the NH4Cl-NH3-H2O system with concentrations higher than 10% ammonia, but N-H???O hydrogen bonds between ammonium ions and water molecule took advantage in the system with lower ammonia concentrations. Correspondingly, the phenomena of hydrogen bonding redshift and blueshift was observed respectively compared in NH3?H2O solution. Moreover, the hydrogen bonding structure of the saturated solution was obtained by means of MD simulation. The present work provides some theoretical basis for the separation of ammonium potassium chloride.     

Understanding hydrological processes in a highly stressed granitic aquifer in southern India

The results of a study evaluating the recharge/discharge conditions of an unconfined stressed granitic aquifer situated in a semi‐arid region of Andhra Pradesh, Southern India are presented. Over the last three decades, excessive withdrawal of groundwater has drastically lowered the water table to the bedrock. The watershed studied was divided into four zones based on geomorphology and hydrogeological conditions. Using environmental chloride data pertaining to groundwater, soil depth profiles, and some hydrogeologic and hydrochemical observations, a recharge model for the watershed was developed. The model revealed that the bulk of the vertical recharge in the western elevated land occurs through preferred pathways and that a small fraction occurs through the soil matrix. In addition, the watershed has a poor hydrogeologic fabric, as indicated by the small range of matrix flow recharge (1 to 1·5% of rainfall) among the four zones. The dominating preferential flow was high (～16% of the annual average rainfall) in the valley fills, but decreased to 5–5·5% in the plains. Furthermore, although the bulk of the recharge occurs vertically, considerable lateral movement of groundwater down the slope indicates that sequential hydrochemical changes occur. Distinct geomorphological features that exist in the watershed support the proposed model. Situations similar to those described above may exist in numerous watersheds in the granitic hard rock region; therefore, information obtained from investigations conducted in this watershed can aid in the development of plans enabling the sustainable exploitation of watersheds that have not yet been developed, as well as implementation of appropriate rainwater conservation measures in over‐exploited watersheds. Copyright © 2009 John Wiley & Sons, Ltd.     

Geomorphic controls on deposition of salt in the Greater Tamar Catchment,northeast Tasmania

In Tasmania, most salts in the landscape originate from rainfall and accumulate in landscapes after evaporation occurs. The distribution and quantity of salt in rainfall from an array of bulk deposition collectors in the Greater Tamar Catchment were assessed for the period September 2013 to August 2014. The bulk deposition samples were analysed for pH, electrical conductivity, major ions (Ca, Mg, Na, SO₄ and Cl) and a selection of trace ions. The average salt flux across the study area was 79 ± 10 kg/ha/yr region, ranging from 170 ± 12 kg/ha/yr near the coast in the north to 42 ± 6 kg/ha/yr inland. Deposition of most ions decreased from the northwest to the south and east, and peaked in winter and spring. Geomorphic factors such as elevation and topography have an important effect on the volume of rainfall and flux of salt from windblown dust and oceanic aerosols. A comparison of measured chloride and salt deposition in Tasmania with other Australian atmospheric studies indicates that continental-scale models of salt flux are not appropriate for Tasmania. New models are proposed that take into account the influence of the Southern Ocean, Tasman Sea and topographic variation in the study area. The results provide improved estimates of rainfall-derived salt inputs to catchments in northeast Tasmania and enable more accurate salt budget modelling. Improved understanding of volumes and distribution of salts has implications for the management of soils and infrastructure that degrade as a result of dryland salinity in Tasmania.     

LiCl-MgCl2-H2O及其子体系多温下体积性质研究(英文)

用高精度振动管密度仪测定二元系统(Li Cl-H₂O和MgCl₂-H₂O)和三元系统(Li Cl-MgCl₂-H₂O)在273.15至308.15 K下溶液密度。采用VFT方程关联了Li Cl和MgCl₂溶液密度与温度、摩尔浓度关系。利用Young理想混合规则,根据二元体积性质计算计算了三元系统溶液密度。采用Pitzer离子相互模型拟合了Li ClMgCl₂-H₂O,得到Pitzer单盐参数(β_M~(_X⁰ V),β_M~(_X¹ V),and C^V_MX,MX=Li Cl和MgCl₂)和混合离子相互作用参数(θ^V_Li,Mg、ψ^V_Li,Mg,Cl     

离子色谱法同时测定天然碱矿中氯离子和硫酸根离子

通过测定氯离子和硫酸根离子可以确定天然碱矿中石盐和芒硝的含量,目前分析方法比较少,且流程冗长,容易污染,生产效率低。本文建立了离子色谱-抑制电导法测定天然碱矿中氯离子和硫酸根的分析方法。样品中水溶性阴离子经热水溶解进入溶液,以30 mmol/L氢氧化钾溶液作为淋洗液,利用AG19阴离子保护柱、AS19阴离子分离柱分离样品中的氯和硫酸根,CRD 200碳酸盐消除装置去除了碳酸根的干扰。方法检出限氯离子为0.01 mg/L,硫酸根为0.02 mg/L;加标回收率为100.9%～104.1%;精密度(RSD,n=10)小于2.5%。实际样品分析结果与滴定法的测定值基本吻合。本法操作简单,重现性好,灵敏度高,结果可靠,不受样品复杂组分及形成缓冲溶液体系的干扰,很好地解决了传统方法费时、耗材、不能同时测定氯离子和硫酸根的问题。