Potassium alum and aluminum sulfate micro-inclusions in polar ice from Dome Fuji,East Antarctica

Water-soluble trace constituents affect the physicochemical properties of polar ice. Their structural distribution provides important insights into the formation history of ice and inclusions. We report the first finding of KAl(SO₄)₂·12H₂O (potassium alum) and Al₂(SO₄)₃·nH₂O (aluminum sulfate) micro-inclusions in the Dome Fuji ice core, East Antartica, using a micro-Raman technique. Eutectic temperatures of these water-soluble species determined using thermal analysis were −0.4 °C for potassium alum and −8.0 °C for aluminum sulfate. Although the formation process of the aluminum-bearing sulfates remains unclear, the occurrence of these salts largely depends on ice depth.     

Preparation,Characterization and Pharmacokinetics of Fluorescence Labeled Propylene Glycol Alginate Sodium Sulfate

A rapid and sensitive fluorescence labeling method was developed and validated for the microanalysis of a sulfated polysaccharide drug,namely propylene glycol alginate sodium sulfate （PSS）,in rat plasma.Fluorescein isothiocyanate （FITC） was selected to label PSS,and 1,6-diaminohexane was used to link PSS and FITC in order to prepare FITC-labeled PSS （F-PSS） through a reductive amination reaction.F-PSS was identified by UV-Vis,FT-IR and ^1H-NMR spectrum.The cell stability and cytotoxicity of F-PSS were tested in Madin-Darby canine kidney （MDCK） cells.The results indicated that the labeling efficiency of F-PSS was 0.522%±0.0248% and the absolute bioavailability was 8.39%.F-PSS was stable in MDCK cells without obvious cytotoxicity.The method was sensitive and reliable; it showed a good linearity,precision,recovery and stability.The FITC labeling method can be applied to investigating the absorption and metabolism of PSS and other polysaccharides in biological samples.     

Research on Corrosion Effect of Sulfate Ions on Concrete Under Wetting-Drying Cycle

Saline soil is widely distributed in the marine sediments along the coast of the world and the arid-semi-arid areas of the Middle East and Iraq,and calcium sulfate erosion has become one of the important factors affecting the durability of concrete in this area.In order to clarify the mechanism of sulfate ion damage to concrete,this paper mainly takes saline soil with high sulfate content in coastal area as well as arid-semi-arid area as the research object,and uses indoor geotechnical test,field test and numerical simulation to study the influence of different dry-wet cycle times on the unconfined compressive strength of concrete test blocks,and puts forward the relationship between the erosion arrival depth and time of sulfate ion in concrete,so as to predict the long-term erosion depth by using the erosion depth of sulfate ion in concrete in short time.The results show that the shorter the erosion time when the erosion reaches a certain depth,and the larger the erosion reaches when the erosion time is the same,the faster the erosion reaches the depth with the increase of erosion time.Compared with rectangular section concrete,circular section concrete penetrates faster.The results of this study can provide a reference for the durability design of concrete in saline soil sites containing sulfate.     

膏盐层在云南会泽和毛坪铅锌矿成矿中的作用：硫同位素证据

云南会泽和毛坪铅锌矿床位于扬子地块西南缘川-滇-黔铅锌多金属矿集区的中南部,小江断裂带、昭通-曲靖隐伏断裂带和垭都-紫云断裂带的构造复合部位,是我国著名的MVT型铅锌矿床。本文以会泽和毛坪铅锌矿为例,系统研究了矿床中矿石硫化物、矿区相关碳酸盐岩地层中微量硫酸盐(CAS)以及外围不同时代膏盐层中石膏的硫同位素组成,探讨了膏盐层在云南会泽和毛坪铅锌矿成矿中的作用。会泽矿床矿石硫化物的δ~(34)S_(V-CDT)值为11.0‰~20.0‰,多数集中在13.0‰~17.0‰之间,平均14.7‰,大致代表总硫的同位素组成。石炭系碳酸盐岩地层中微量硫酸盐的δ~(34)S_(V-CDT)值为10.4‰~18.6‰,平均13.1‰,较矿石硫化物的值稍低。矿区外围石炭系膏盐层中石膏的δ~(34)S_(V-CDT)值为12.9‰~17.1‰,平均13.6‰,与石炭系碳酸盐岩中微量硫酸盐的δ~(34) S_(V-CDT)值几乎完全一致。毛坪矿床矿石硫化物的δ~(34)S_(V-CDT)值与其赋存层位密切相关,赋存于摆佐组(C1b)的矿石硫化物的δ~(34)S_(V-CDT)值为7.1‰~17.5‰,平均12.8‰,较会泽矿石硫化物的值稍低,与石炭系碳酸盐岩地层中微量硫酸盐和石膏的值一致;赋存于宰格组(D3zg)的矿石硫化物的δ~(34)S_(V-CDT)值为18.3‰~22.7‰,平均21.1‰,与赋存于摆佐组(C1b)的矿石硫化物的值和会泽矿床矿石硫化物的值明显不同。矿区外围宰格组(D3zg)膏盐层中石膏的δ~(34)S_(V-CDT)值为21.9‰~25.9‰,平均23.6‰,与毛坪矿床宰格组(D3zg)矿石硫化物的值相似。通过对比会泽、毛坪矿床中不同赋矿层位矿石硫化物、石炭系不同层位碳酸盐岩中微量硫酸盐和矿区外围不同时代膏盐层中石膏的硫同位素组成及变化规律,提出会泽、毛坪铅锌矿床矿石硫化物中的硫主要来源于赋矿层位膏盐层中石膏硫酸盐的热还原。其中会泽铅锌矿的硫绝大部分来自石炭系膏盐层,只有10%的硫来自下伏的宰格组膏盐层;毛坪铅锌矿床中赋存于宰格组的矿体,矿石硫主要来自宰格组膏盐层,而赋存于摆佐组的矿体,矿石硫主要来自摆佐组膏盐层,即膏盐层是在原地被还原的。成矿作用分为两个阶段,第一阶段石膏与甲烷等有机质发生热化学反应,全部被还原形成H2S,储存在层间裂隙或溶洞之中,同时发生大规模白云岩化;第二阶段淋滤了深部基底岩石中Pb、Zn等金属成矿物质的成矿流体与储存在层间裂隙或溶洞之中的富含H2S的流体混合,形成黄铁矿、方铅矿和闪锌矿等富集沉淀,形成高品位矿石。     

早期成岩作用过程中硫酸盐还原反应研究进展

文章概述近年来早期成岩作用中硫酸盐还原反应研究的某些新资料和新成果 ,综合分析了各种沉积环境下的早期成岩作用中的硫酸盐还原反应。重点论述贫氧缺氧条件下的反应机制。并讨论了判别沉积环境的Fe -C -S的关系及黄铁矿的形成和碳酸盐的溶解、沉淀与氧化还原带的对应关系。简要讨论了早期成岩作用中硫酸盐还原反应的研究意义。     

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。     

The Effect of Additives on Calcium Sulfate Dihydrate Crystallization Kinetics in Gypsum Type Brine System

正1 Introduction There exist calcium and sulfate ions outside sodium chloride in solution mining for calcium sulfate brine.The calcium and sulfate ions not only affect the purity of the vacuum salt products,but also increase the scaling of vacuum evaporation tanks and brine reusing pipes.Additives have certain impacts on the crystallization dynamics(Randolph et al.,1971).The crystallization     

Hydrochemistry of Salt Lakes in Southeastern Transbaikalia(Russia) in the Time of Arid Phase of Climate Change at the Beginning of the XXI Century

正1 Introduction In the south of Eastern Transbaikalia in the border area with China and Mongolia,there are at least 300 saline without outlet lakes.They are confined to the semi-arid zone Daurian steppes with pronounced continental salinization processes and are mostly located on the bottoms of the intermountain basins.Their origin is related to evaporative concentration of fresh waters lakes filling.     

Advances in Re-Os Isotopic Dating in Geochronology of Hydrocarbon Accumulation

Rhenium-Osmium (Re-Os) isotopic dating applied to the geochronology of hydrocarbon accumulation has been the forefront of international research in the last 10 years and has achieved significant achievements. However, our current researches are lacking in Re-Os isotopic chronology on the geochronology of hydrocarbon accumulation. The successful application of the Re-Os geochronology has enabled the determination of accurate and precise depositional ages for Organic-Rich Sedimentary rocks (ORS), the establishment of timing constraints of oil generation or migration, and the fingerprinting of the source of oil. On the basis of literatures study both at home and abroad, this article mainly dealt with the principle of Re-Os isotopic dating and analyzed the accumulation processes of Re and Os in a seawater-sediment system. Meanwhile, the test samples, sample preparation and analytical methodology of Re-Os isotopic dating were summarized. The results revealed that the initial ¹⁸⁷Os/¹⁸⁸Os ratio could constrain the age of oil generation or migration, and effectively evaluated the relationship between source rock and oil. The radiogenic ¹⁸⁷Os/¹⁸⁸Os ratio showed a positively correlated relationship with source rock age. This article proposed that hydrocarbon mature, biodegradation and water washing had minimal or no effect on data scatter about Re-Os isochron. However, the effects of postdepositional mobility of Re and Os, variations in the initial ¹⁸⁷Os/¹⁸⁸Os ratio, and thermochemical sulfate reduction could result in data scatter. The reproducibility and accuracy of Re-Os age was also closely related to the sample particle size and sample amount. Compared with other isotopic dating, the biggest advantage of Re-Os isotopic dating is to study geological body related to accumulation process, and to obtain direct evidence of hydrocarbon accumulation period. From what was discussed above, the article discussed the existing problems and put forward the future hot research and development direction of Re-Os isotope system, so as to promote the deep development of relative theory and technology of Re-Os isotopic dating.     

内蒙古额济纳盆地硫酸盐沉积物中δ17O异常及其指示意义

为探析我国干旱地区地表硫酸盐沉积物中δ17O异常的存在及其变化特征,在西北额济纳盆地采集地表盐结层、现代风尘土、湖底沉积物和盐池土壤四种不同类型的硫酸盐沉积物样品。利用硫酸银(Ag2SO4)热解法同时测定硫酸盐样品中的δ17O和δ18O值,其δ17O、δ18O和Δ17O的分析精度分别为0.5‰、0.3‰和0.1‰。研究发现:(1)四种不同硫酸盐沉积物中均存在δ17O异常,其Δ17O值为0.2‰~1.0‰,这表明具有δ17O异常的硫酸盐能够从大气圈转移到陆壳矿物中,并在特定的地表环境中累积起来;(2)西戈壁的吉格德查盐池土壤剖面上硫酸盐Δ17O值随深度增加而增大,变化范围为0‰~0.6‰,这可能是干旱区极其有限的降水淋滤作用使具有较大Δ17O值的硫酸盐优先淋滤的结果,这种分离效应揭示的是在干旱的气候条件下,硫酸盐在土壤剖面上分离的过程。本研究证明我国干旱沉积环境中的硫酸盐δ17O异常的存在,为大气中臭氧(O3)和过氧化氢(H2O2)的氧同位素异常能够转移到地表矿物中提供新的证据,为地表沉积物中硫酸盐的来源、迁移、混合及沉积后的变化提供有效信息。