X射线荧光光谱法测定重晶石中的硫酸钡方法研究

应用XRF可快速测定重晶石中钡元素的总量,但当测定硫酸钡含量时,由于样品中的碳酸钡计入钡量造成硫酸钡的测定结果不准确,铜、铅、锌等有色金属元素对熔样坩埚会造成损害,需要进行酸处理除去碳酸钡、铅等干扰。而样品经酸处理后不同样品的剩余量不同,造成熔剂与样品的比例不确定,也不能准确测定硫酸钡的含量,因此保证熔剂与样品比例一致是解决该问题的关键。本文优化了样品前处理、熔片制样和仪器工作条件,将一定量样品以10%盐酸和10%硝酸溶解,过滤除去碳酸钡、硫酸钙及铜、铅、锌等有色金属元素,未溶解样品在700℃下灼烧后以氧化铝补充到原取样量,实现了熔剂与样品比例一致,再以硝酸铵作氧化剂,溴化锂和碘化铵作脱模剂,1075℃熔融制片,即可用XRF准确测定硫酸钡的含量。本方法的相对标准偏差(RSD)小于0.4%,检出限为72μg/g,较ICP-OES等方法的检测周期短、干扰元素少,提高了测试效率和分析质量。     

活性MgO碳化固化土的抗硫酸盐侵蚀性研究

既有研究表明,活性MgO固化土经CO2碳化几小时后其强度能达到甚至超过28 d的水泥固化土强度,碳化反应生成镁的碳酸化合物能有效降低固化土的含水率和孔隙率,提高土颗粒胶结能力。通过室内试验进一步研究碳化固化土的抗硫酸盐侵蚀特性。采用硫酸钠溶液、硫酸镁溶液浸泡碳化固化土,对浸泡不同龄期后的碳化固化土进行无侧限抗压强度试验和微观测试（XRD,SEM和MIP）,并与硫酸盐侵蚀后的水泥固化土进行试验对比。结果表明：活性MgO固化粉土碳化3 h,试样的无侧限抗压强度可达5 MPa左右,经硫酸盐溶液浸泡28 d后其强度基本保持不变,试样质量变化也不大;而水泥土试样的早期强度（7 d）则有一定增长,随龄期增长,强度大大降低,质量则明显增长。通过对硫酸盐侵蚀前后的碳化土的微观机制分析,发现活性MgO碳化固化土中的镁碳酸化合物的化学成分并未发生明显变化,孔隙结构也未明显改变,从而保证其强度稳定。因此,活性MgO固化粉土碳化后具有比水泥固化土更强的抗硫酸盐侵蚀能力。     

硫酸镁对硼酸介稳区性质的影响

通过浊度法测定10℃～45℃范围内MgSO4-H3BO3-H2O体系中硼酸的溶解度及介稳区宽度,得到硼酸的成核方程,并计算其表观成核级数。实验结果表明,硫酸镁的存在降低了硼酸的溶解度;随着硫酸镁浓度的升高,硼酸的介稳区宽度先变宽后变窄;硫酸镁的加入使硼酸的表观成核级数增加。     

山西省盂县羊泉冶镁白云岩矿床地质特征、成因及经济意义研究

金属镁是新世纪重要的绿色金属能源,而冶镁白云岩是生产金属镁不可缺少的原料,是山西省能源重化工基地的一种十分重要的矿产资源.盂县羊泉冶镁白云岩矿床位于吕梁、太行断块-五台山块隆东侧,白云岩矿体赋存于寒武系上统-奥陶系下统三山子组,总体上呈走向NW、倾向SW的单斜构造.含矿岩石主要为中-厚层细-粗晶白云岩,粉晶-细晶或中粗晶粒状结构,块状或薄层状构造.矿床的形成演化经历了沉积-白云岩化-重结晶三个阶段.矿体平均品位ω(MgO)为21.20％、ω(SiO2)为0.67％、ω(K2O+ Na2O)为0.076％,品位变化较均匀.该区共求得冶镁用白云岩矿资源量约3.45亿吨,属一大型矿山,具有较大的开发前景.     

Identifying the Sources of Solutes in Karst Groundwater in Chongqing,China: a Combined Sulfate and Strontium Isotope Approach

Groundwater from karst subterranean streams is among the world’s most important sources of drinking water supplies, and the hydrochemical characteristics of karst water are impacted by both natural environment and people. Therefore, the study of hydrochemistry and its solutes’ sources is very important to ensure the normal function of life support systems. In this paper, thirty?five representative karst groundwater samples were collected from different aquifers (limestone and dolomite) and various land use types in Chongqing to trace the sources of solutes and relative hydrochemical processes. Hydrogeochemical types of karst groundwater in Chongqing were mainly of the Ca?HCO3 type or Ca (Mg)?HCO3 type. However, some hydrochemical types of karst groundwater were the K+Na+Ca?SO4 type (G25 site) or Ca?HCO3+SO4 type (G26 and G14 site), indicating that the hydrochemistry of these sites might be strongly influenced by anthropogenic activities or unique geological characteristics. The dissolved Sr concentrations of the studied groundwater ranged from 0.57 to 15.06 μmmol/L, and the 87Sr/86Sr varied from 0.70751 to 0.71627. The δ34S?SO42? fell into a range of ?6.8‰?21.5‰, with a mean value of 5.6‰. The variations of both 87Sr/86Sr and Sr values of the groundwater samples indicated that the Sr element was controlled by the weathering of limestone, dolomite and silicate rock. However, the figure of 87Sr/86Sr vs. Sr2+/[K++Na+] showed that the anthropogenic inputs also obviously contributed to the Sr contents. For tracing the detailed anthropogenic effects, we traced the sources of solutes collected karst groundwater samples in Chongqing according to the δ34S value of potential sulfate sources. The variations of both δ34S and 1/SO42? values of the groundwater samples indicated that the atmospheric acid deposition (AAD), dissolution of gypsum (GD), oxidation of sul?de mineral (OS) or anthropogenic inputs (SF: sewage or fertilizer) have contributed to solutes in karst groundwater. The influence of oxidation of sul?de mineral, atmospheric acid deposit and anthropogenic inputs to groundwater in Chongqing karst areas was much widespread.     

碳还原法分析硫酸盐的氧同位素组成

硫酸盐矿物是自然界最常见矿物,也是自然界少数具有氧同位素非质量分馏效应的矿物之一.硫酸盐矿物的氧同位素组成可以为研究其形成过程和生成条件提供大量信息.目前,在国内外分析硫酸盐氧同位素的3种方法中,碳还原方法乃是分析硫酸盐中氧同位素组成的最精准方法.本次研究建立了分析硫酸盐中氧同位素组成的碳还原方法,介绍了硫酸钡的分析流...     

活性MgO定量分析标准方法的比较研究

用WB和JC标准水合法测定轻烧MgO粉的活性MgO含量,对测定结果进行方差和误差分析,并研究了水化时间对测定结果的影响。结果表明,两种方法存在显著性差异,WB和JC水合法的平均相对误差分别为1.31%和-19.85%,WB水合法精密度远高于JC水合法。以WB水合法为基准,JC水合法的平均相对误差大于-20%,远远超过行业标准中规定的±3%。因此,对于镁水泥原料MgO中活性含量的定量分析,不能采用JC方法,必须采用WB方法。此外,发现水化3 h已经接近活性氧化镁的水化平衡,为修订WB标准方法提供了参考依据。     

九龙江河口沉积物中硫酸盐还原与甲烷厌氧氧化:同位素地球化学证据

通过沉积物柱孔隙水中甲烷,SO2-4,Cl-,δc(34S-SO2-4)、δc(13 C-CH4)的垂直分布特征,研究了硫酸盐还原和甲烷厌氧氧化(anaerobic oxidation of methane,简称AOM)过程在九龙江河口沉积物中的分布规律.测定结果显示两个站位(J-A和J-E)间隙水中SO2-4浓度随深...     

西藏嘎拉勒铜金矿床地质特征及矽卡岩矿物学特征研究

嘎拉勒铜金矿床位于班公湖-怒江缝合带西段,是该带上新近发现的十分重要的矽卡岩(斑岩)型铜金矿床,其金资源量已达大型以上规模。矿区内出露地层有白垩系朗久组及捷嘎组,并发育大量燕山期中酸性侵入岩。矿体主要产于灰白色花岗闪长岩与白云岩或白云质大理岩的接触带矽卡岩内。矽卡岩主要呈层状、似层状、港湾状及不规则状等产出;矽卡岩矿物主要为橄榄石、蛇纹石、辉石、金云母、透闪石、绿帘石、水镁石等;靠近内接触带可见石榴子石;金属矿物主要有磁铁矿、自然金、黄铜矿、斑铜矿、辉铜矿、辉钼矿等。电子探针分析表明,矿区内矽卡岩矿物中的橄榄石主要为镁橄榄石,辉石主要为透辉石,云母主要为金云母,由此构成的矽卡岩矿物组合为典型的镁质矽卡岩;与之伴生的钙质矽卡岩矿物石榴子石主要为钙铁榴石。矿区中的矽卡岩在空间上具有较好的分带性,其表现为从内接触带至外接触带经历了镁橄榄石-透辉石相至金云母-透闪石相的渐变过渡演化,表明矿区矽卡岩具有从高温至低温的矿物组合演化序列;与矽卡岩分带相伴随的矿化分带,表现为深部的铜(钼)矿化过渡到浅部的铜金矿化。矿区最新勘查成果显示,在深部已发现少量斑岩型矿化,显示存在统一的矽卡岩-斑岩成矿系统的可能性,深部找矿潜力较大。     

Factors Controlling Precipitation of Barite and Witherite and Genesis of the Ankang–Xunyang Barium Deposits, Shaanxi, China

The barium deposits in Ankang and Xunyang counties,Shaanxi Province,China,occur in the northernmost part of the world-class barium metallogenic belt in south Qinling.The deposits are hosted by the Lower Silurian carbonaceous siliceous rocks,with a unique combination of barite and witherite.The homogenization temperatures of fluid inclusions in the barite are mainly concentrated between 135 and 155 ℃,whereas those from the witherite have two peaks of 165-175 ℃,and 215-225℃,respectively.Laser Raman analysis of fluid inclusions indicates that the vapor phase of fluid inclusions in barite is dominated by H_2O,although some contains N_2,H_2S,and CH_4.The compositions of the vapor and liquid phases of fluid inclusions in witherite can be divided into two end-members,one dominated by H_2O without other volatiles,and the other containing CH_4,C_2H_6,C_3H_8,C_2H_4,and C_6H_6 in addition to H_2O.CO_2,H_2S,and some CH_4 are interpreted as products of chemical reactions during mineralization.Organic gases(CH_4,C_2H_6,C_3H_8,C_2H_4,and C_6H_6) in the fluids were critical in the formation of barium sulfate versus carbonate.The δ~(34)S values of barite range from 38.26‰ to54.23‰(CDT),the δ~(34)S values of sulfides coexisting with barium minerals vary from 22.44‰ to25.11‰(CDT),and those in the wall rock from 11.60‰ to 19.06‰(CDT).We propose that the SO_4~(2-)generally experienced bacterial sulfate reduction in seawater before mineralization,and some SO_4~(2-)also experienced thermochemical sulfate reduction in hydrothermal system during mineralization.The δ~(13)C values of witherite range from-27.30‰ to-11.80‰(PDB),suggesting that carbon was sourced from organic substances(like CH_4,C_2H_4,and C_2H_6).The formation of witherite was possibly associated with thermochemical sulfate reduction,which caused the consumption of the organic gases and SO_4~(2-) in the hydrothermal solutions,consequently inhibiting barite formation.The important conditions for forming witherite include high fluid temperatures,high Ba~(2+) concentrations,CO_2 in the fluids,low HS~- concentrations,and the subsequent rapid diffusion of H_2S during thermochemical sulfate reduction of the fluids.