电子探针分析与系列矿物研究

本文论述以电子探针为主要测试手段对下述几种系列矿物的研究成果:(1)铂族元素系列矿物的研究(包括Ru-Os-Fe金属互化物矿物系列和RuAs_2-OsAs_2二元固溶体矿物系);(2)Au-Cu系列矿物的研究;(3)黝铜矿族矿物的研究。     

胶磷矿晶体结构研究

详细叙述了磷灰石的晶体结构,并采用多种方法对磷灰石结构中配位多面体各元素间的化学键力进行计算,分析了磷灰石的表面特性。针对贵州典型磷矿区具有代表性的胶磷矿试样,其主要由微晶磷灰石组成,采用x射线衍射分析了胶磷矿试样的物相组成、结晶度、晶胞参数以及磷灰石晶粒大小。在扫描电子显微镜下,2种胶磷矿多呈集合体形态,两种胶磷矿中磷酸盐矿物主要为氟磷灰石。     

绿柱石的辐照赋色与效应

利用电子加速器为辐照源，对四川，新疆等产的无色绿柱石进行了辐照改色处理。在改色实验中，对辐照源的输出功率，电子能量，扫描面积，扫描速度，辐照剂量等参数，及辐照后样品的辐照效应，环境适应性，时效考验等特性进行了较系统的实验研究，并拟定出一套适合不同成因的无色绿柱石辐照改色的优选方案，对绿柱石的辐照机制和应效进行了探讨。     

大别山地区沙坪沟斑岩型钼矿床蚀变及矿化特征研究

沙坪沟钼矿床是大别山地区新近发现的、世界第二大的斑岩型钼矿床。本文在前期以及前人的工作基础上,通过详细的野外地质观察和系统的岩相学、矿相学以及探针测试分析工作,详细研究了沙坪沟钼矿床的蚀变与矿化特征。结果表明,沙坪沟钼矿床的围岩蚀变类型主要有钾硅酸盐化、青磐岩化和绢英岩化,绢英岩化又可细分为以石英为主和以绢云母为主。矿床中产出16种脉体类型,根据矿床的脉体类型划分了4个成矿阶段:(1)石英-钾长石阶段;(2)石英-硫化物阶段;(3)石英-绢云母阶段;(4)石英-萤石-石膏阶段。蚀变及矿化特征显示,沙坪沟钼矿床的钼矿化开始于石英-钾长石阶段晚期,结束于石英-绢云母阶段早期,石英-硫化物阶段是辉钼矿主要的形成阶段。沙坪沟钼矿床经历了多期次脉动式成矿流体的蚀变与矿化过程,在不同蚀变-矿化阶段中,成矿流体的物化条件和组分的变化是控制各阶段蚀变类型和脉体中矿物组合的主要因素。产于以伸展为主的板内环境的沙坪沟钼矿床与其他构造环境下的斑岩钼矿床在与成矿关系密切的岩石、蚀变分带等方面相似,但由于围岩性质的差异,矿体赋存位置及产状不同;而在矿物种类、矿化产出位置及产状、与矿化关系最为紧密的蚀变类型等方面存在差异。斑岩型钼矿床的构造背景可能控制了其岩浆的形成、演化以及含矿性,而岩浆岩最终定位的深度、围岩等条件也是控制蚀变和矿化特征的重要因素。     

X射线衍射和电子探针技术在矿物药雄黄鉴定及质量评价中的应用

雄黄是我国常用的矿物类中药,由于晶体空间结构不同,可分为α雄黄(AsS)和β雄黄(As4S4)。雄黄受氧化作用会产生剧毒物质砒霜(As2O3),其中β雄黄因空间结构关系更易被氧化,因此对矿物药雄黄的成分鉴定和质量评价具有重要的意义。常用的分析雄黄中砷及其他元素的方法(原子吸收光谱法、电感耦合等离子体质谱法、高效液相色谱-质谱法等)是通过测定总砷、价态砷和其他相关元素实现对雄黄的鉴别和有害成分的检测,分析过程复杂,试剂消耗大,需对样品进行破坏,而且不能直接对矿物结构进行判定。本文采用薄片鉴定、X射线衍射和电子探针对来自代表性生产地贵州思南和湖南石门的6种药用雄黄样品进行鉴别和质量评价。首先通过薄片鉴定初步确定雄黄样品的主要成分及伴生矿物,进一步利用X射线粉晶衍射和电子探针技术对雄黄的主要成分、伴生矿物进行半定量分析,再利用电子探针研究雄黄中As、S、O等元素的赋存状态,在这些技术综合鉴定的基础上,对收集的雄黄进行质量评价。分析结果显示:产自贵州思南的1号矿药由石英(82.8%)、方解石(9.5%)和白云石(7.7%)组成,2号矿药由α雄黄(64.7%)和石英(35.3%)组成;产自湖南石门的6号矿药由β雄黄(86.5%)和电气石(13.5%)组成,3号和4号矿药由α雄黄单矿物组成,5号矿药由β雄黄单矿物组成,3号、4号和5号三个样品中As含量大于70%,符合药典规定;电子探针分析样品中均未检测到砒霜,总体上表明湖南产的雄黄品质较高。研究表明,X射线粉晶衍射法利用了衍射图谱与晶体结构的一一对应性,找到不同矿物药样品的专属特性,而对于多组分矿物药样品,只要混合组分恒定,其衍射图谱就相对稳定,具有指纹特征;电子探针利用As、O等元素的赋存状态,可以有效地对雄黄的质量进行评价。X射线衍射和电子探针技术的结合用于鉴定雄黄矿物药是一种极为有效、可行的办法,与传统方法相比更为快速、经济。     

青海尕林格铁矿床矽卡岩矿物学及蚀变分带

尕林格矽卡岩型铁多金属矿床位于青海省西部祁曼塔格成矿亚带的中部.矿体处于花岗闪长岩与滩间山群白云质大理岩接触带内以及外接触带沿NWW向断裂构造破碎带分布的大理岩和蚀变安山岩内.从侵入接触带往东,蚀变岩石分带性明显,主要划分出3种含矿矽卡岩带:含Fe的镁质矽卡岩带,含Fe、Cu的钙质矽卡岩带,含Fe、Pb、Zn的锰-钙质矽卡岩带.镁质矽卡岩带的矽卡岩矿物主要包括镁橄榄石及其蚀变矿物蛇纹石、粒硅镁石、透辉石、斜绿泥石,有关的金属矿物主要为磁铁矿.钙质矽卡岩带的主要矽卡岩矿物有绿钙闪石、铁阳起石、钙铁辉石、铁叶绿泥石、磷灰石、中长石,有关的金属矿物为磁铁矿、磁黄铁矿和少量黄铜矿.与锰-钙质矽卡岩有关的矽卡岩矿物有锰钙铁辉石、钙铁榴石、钙铝榴石、铁镁绿泥石、绿帘石、硅灰石、磷灰石、钙长石等,金属矿物有方铅矿、闪锌矿、磁铁矿和磁黄铁矿.通过对矿物组合的研究,确定了不同矿物组合的生成关系,划分了成矿期次,分为矽卡岩期、退化蚀变期和金属硫化物期,矽卡岩期又分为早、晚2个阶段.矽卡岩早期生成的石榴子石的化学成分端员以钙铝榴石(Gro67～ 99)为主,辉石的成分端员以透辉石(Di96～ 98)为主;矽卡岩期晚期阶段石榴子石的化学成分端员以钙铁榴石(Ad78～98)为主,辉石的成分端员以钙铁辉石(Hd68～ 84)为主.与中国东部矽卡岩型矿床进行对比后发现,锰-钙质矽卡岩带是一种向锰质矽卡岩带过渡的类型,对于寻找与锰质矽卡岩有关的矿化类型具有指示意义.     

Biomass Burning in Southern Africa: Individual Particle Characterization of Atmospheric Aerosols and Savanna Fire Samples

Ambient atmospheric aerosols and savanna fireparticulate emission samples from southern Africa werecharacterised in terms of particle classes and theirnumber abundance by electron probe X-ray microanalysis(EPXMA). About ten particle classes were identifiedfor each sample. The major classes werealuminosilicates and sea salts for ambient coarse(2–10 m equivalent aerodynamic diameter (EAD))samples, and K-S and S-only particles for ambient fine(<2 m EAD) samples. The K-S particles are oneof the major products of biomass burning. The EPXMAresults were found to be consistent with the resultsfrom bulk analyses on a sample by sample basis. Forsavanna fire fine samples, quantitative EPXMA revealedthat many particles had a composition of simple saltssuch as KCl. Some particles had a deviatingcomposition in the sense that more ionic species wereinvolved in sustaining the balance between cations andanions, and they were composite or mixed salts.Because of extensive processing during the atmospherictransport, the composition of the K-S particles in theambient samples was different from K₂SO₄,and such particles were enriched with S. The finepyrogenic KCl particles and the fine sea-saltparticles were much depleted in chlorine.     

SEM-EDX Characterisation of Tropospheric Aerosols in the Negev Desert (Israel)

Individual aerosol particles collected in the Negev desert in Israel during a summer and winter campaign in 1996–1997 were analysed by scanning electron microscopy with energy-dispersive X-ray analysis. Hierarchical cluster analysis was performed to interpret the data on the basis of particle diameter and composition. Eleven particle classes (groups) provided clues on sources and/or particle formation. The summer samples were enriched in sulphates and mineral dusts; the winter samples contained more sea salts, aged sea salts, and industrial particles. The fine size fraction below 1 m diameter was enriched in secondary particles and showed evidence of atmospheric processing. The secondary sulphate particles were mainly attributed to long-range transport. A regional conversion from calcite to calcium sulphate occurred during summer. Industrial particles originating from local pollution appeared during winter.     

Characterisation of Soot Emitted by Domestic Heating,Aircraft and Cars Using Diesel or Biodiesel

The characterisation of aggregates, like soot, firstly requires the determination of the size distribution of the primary particles. The primary particle size of combustion generated aggregates depends upon the combustion environment and the formation conditions, such as temperature, pressure and fuel-to-air ratio, among others. Since the combustion characteristics are different in the different types of burners, the characterisation of primary particles may offer the possibility to distinguish soot from different sources. In this paper, we present the signature of the primary particles and the aggregates of soot emitted by cars using diesel or biodiesel, by domestic heating, and by aircraft exhausts, which can be considered as the major sources as derived from measurements on transmission electron micrographs. The size distributions of all aggregates types with different aerodynamic diameter were log-normal and quasi-monodisperse. The size distribution of the primary particles for soot emitted by different sources showed minor differences. However, a comparison between the diameter of the primary particles and those obtained using a standard method for carbon black revealed discrepancies. The median diameter of the primary particles was combined with the median number of primary particles in an aggregate to calculate the relative particle surface area available for adsorption. In a similar way, the relative specific surface area was determined. The surface area was measured using the Brunauer-Emmett-Teller (B.E.T.) nitrogen adsorption method and the relative surface area available for adsorption was calculated.     

计算高能原电子能量损失率的方法

提出了计算属于同一个能区高能原电子在金属发射体内的沿程能量损失率的方法,用实验数据分别计算出属于两个能区的高能原电子在金属金发射体内的沿程能量损失率,并用实验数据计算出属于同一个能区的高能原电子在金属铝发射体内的沿程能量损失率,结果显示,计算高能原电子在金属发射体内的沿程能量损失率的方法是可行的.