模拟不同气候条件下碳酸盐岩风化作用的淋溶实验研究

通过模拟干热、湿热与干冷3种气候条件,以饱和CO2水作为淋溶液,对黔中岩溶区3条碳酸盐岩风化壳岩-土界面的岩粉层试样进行了淋溶实验(其中干热、湿热条件下淋溶到残余酸不溶物阶段),对淋出液的pH值以及主要造岩元素的浓度进行了动态分析。结果表明,碳酸盐岩风化壳岩-土界面由岩到土的转变过程中,伴随碳酸盐的溶蚀,酸不溶物已表现出明显的风化倾向。碳酸盐的溶蚀强度表现为干冷>干热>湿热的变化趋势。温度低,碳酸盐的溶解速率大;排水条件好,碳酸盐溶解释放的Ca、Mg易随风化流体排出体系。对于酸不溶物组分,淋溶实验中有:(1)K、Na、Mg、Si、P的载体矿物风化强度在干热条件下最大(至于Ca,由于方解石与白云石均是其主要的载体矿物,酸不溶物相中的Ca难以在淋出液中有效识别)。在干冷与湿热之间,K、Na、Mg等盐基离子的溶出能力大多表现为湿热>干冷,指示了温度对盐基离子释放强度的重要制约作用;而Si和P未表现出一致的变化趋势,可能源于淋溶体系微环境的差异。(2)Fe与Mn表现出弱迁移性。其中,Fe在干冷环境下淋出强度最弱,说明温度是制约含Fe矿物分解速率的重要因素。而Fe在干热与湿热之间,以及Mn在3种淋溶条件下,未呈现出一致的变化趋势。(3)Al和Ti在碳酸盐岩风化过程中表现出强烈的惰性。      

缅甸不同矿点翡翠的矿物学特征

通过对缅甸达木坎矿区、帕敢矿区、隆肯矿区的4个矿点翡翠样品的偏光显微镜、电子探针、X射线粉晶衍射等测试,其结果表明:各矿点翡翠均以粒状变晶结构为主,主要矿物为硬玉,次要矿物有钠长石、云母类、辉石类、闪石类矿物、沸石类矿物等。其中,哥因角矿点翡翠矿石中有较大量辉石类矿物,纳莫矿点发现较大量方沸石矿物。沸石是含水矿物,而含水矿物作为矿脉的前锋组成矿物更为合理,故纳莫翡翠矿体形成深度应相对其它矿点更深。隆肯矿点翡翠样品w(A_l2O_3)=23.187%,w(Na_2O)=17.706%,w(TiO_2)=0.349%,w(K_2O)=0.298%,高于其它矿点;哥因角矿点翡翠样品w(CaO)=1.821%,w(MgO)=2.983%,w(FeO)=1.432%,高于其它矿点;纳莫矿点样品w(SiO_2)平均61.91%,为4个矿点中最高。     

富水破碎岩体注浆加固材料试验研究与应用

针对富水破碎地层注浆治理过程中传统水泥类材料难以实现注浆加固和堵水同步进行的难题,以硫铝酸盐水泥熟料和钢渣微粉为主要原材,成功制备了一种水泥基复合注浆材料（CGM）。通过与传统水泥材料进行性能对比试验,采用扫描电镜和X射线测试手段,分析了CGM材料制备工艺、组分含量和浆液制备条件对材料性能的作用规律,并检验了CGM材料的工程适用性。结果表明：CGM材料宜采用混合粉磨制备工艺,可显著提高其水化活性,且粉磨时间应不超过45 min。钢渣微粉含量越高,水灰比越大,结石体强度越低,凝结时间越长,水灰比超过1.2:1时,结石体后期会出现干缩。与传统水泥材料相比,CGM材料浆液凝结时间与黏度的环境敏感度低,具有显著的工程适用性和性能优越性。     

矿渣微细粉掺量对水泥水化产物的影响

利用X射线衍射、TG-DSC综合热分析以及环境扫描电子显微分析技术等,研究了矿渣微细粉对水泥水化产物钙矾石、Ca(OH)₂、CSH凝胶等的影响规律。研究结果表明,在水化早期,矿渣微细粉即参与水泥水化进程,显著影响水泥水化产物钙矾石、Ca(OH)₂和CSH凝胶等的生成速度和生成量及微观形貌,并且随着其掺量增大及水化时间延长,矿渣微细粉参与水泥水化反应程度逐渐提高。     

电感耦合等离子体质谱-X射线衍射法研究云南玉溪和美国内华达地区黏土型锂资源矿物学特征

中国云南玉溪和美国内华达均已发现大量黏土型锂资源,目前关于两地区样品矿物学特征的研究相对不足,而对黏土型锂资源进行充分的矿物学特征研究是锂提取工作开展的重要前提.本文采用X射线荧光光谱、电感耦合等离子体质谱、X射线粉晶衍射、扫描电镜等分析技术,从化学组成、矿物组成、微观形貌等角度对云南玉溪的两个黏土型锂资源样品(YM-...     

新矿物(19931～199312)

本文以表格形式列举了１９９３年１月至１９９３年１２月经《国际矿物学协会（ＩＭＡ）新矿物与矿物命名委员会（ＣＮＭＭＮ）》批准并在各国矿物学杂志上发表的４２个新矿物的中文英文名称、化学式及其他数据。数据依次为：矿物的晶系、空间群、晶胞参数、主要粉晶数据（Ｉ、ｈｋｌ）、物理性质（晶形、颜色、条痕、光泽、解理、发光、硬度、密度等）、光学性质（一、二轴晶,正、负光性,折光率,反射率,双反射,２Ｖ,色散,吸收性,多色性等）、产状、共生矿物等。     

Structural properties of (Mn1-x Fe x )Nb2O6 columbites from X-ray diffraction and IR spectroscopy

A suite of (Mn_1-x Fe _x )Nb₂O₆ (x=0, 0.05, 0.25, 0.50, 0.75, 1) columbite samples has been prepared by solid-state reaction from oxides. X-ray diffraction and spectroscopic investigations have been carried out in order to gain different perspectives on how the solid solution adapts at different length scales to cation mixing. X-ray powder diffraction and powder absorption IR spectroscopy data are presented. The powder diffraction data show that there is no significant excess volume of mixing on the Fe–Mn columbite join. All the unit-cell parameters decrease linearly as a function of increasing Fe content. Substitution of Fe²⁺ for the larger Mn²⁺ cation causes a decrease in the volume of the A polyhedron, which also becomes more regular with respect to both bond-length and edge-length distortion parameters. No significant variation of the B site has been observed. Wavenumber shifts of the IR peaks nearly all vary linearly with composition, consistent with linear variations of the lattice parameters. Line broadening has been quantified by autocorrelation analysis of the IR spectra. This is interpreted as suggesting that there is some element of local strain or positional disorder at the length scale of second or third nearest neighbours around sites occupied by Fe.     

XEPOS型偏振能量色散X射线荧光光谱仪分析蒙古铁矿石

以熔融玻璃片和粉末压片制样,采用XEPOS型偏振能量色散X射线荧光光谱仪,建立了铁矿石中总铁、氧化钙、氧化镁、二氧化硅、三氧化二铝、硫、磷、铜等组分的快速分析方法。着重讨论硫、磷两元素测定的可行性和Lucas-Tooth、Price数学校正模型的适应性和改善方法的途径。     

罕见的蓝色饵-纳透闪石研究

尽管角闪石在地壳中大量存在 ,但是蓝色钾 钠透闪石却是角闪石中的稀有品种。本文采用X射粉晶线衍射和晶胞参数计算 ,确定该矿物为蓝色的钾 钠透闪石 ,用电子探针 (EMPA)精确分析了它的化学成分 ,确定为钾 钠透闪石 ,而不是蓝色软玉 (即不是透闪石或阳起石 )。     

Kinetic study of the dehydroxylation of chrysotile asbestos with temperature by in situ XRPD

 The kinetics of the dehydroxylation of chrysotile was followed in situ at high temperature using real-time conventional and synchrotron powder diffraction (XRPD). This is the first time kinetics parameters have been calculated for the dehydroxylation of chrysotile. The value of the order of the reaction mechanism calculated using the Avrami model indicates that the rate-limiting step of the reaction is a one-dimensional diffusion with an instantaneous nucleation or a deceleratory rate of nucleation of the reaction product. Hence, the rate-limiting step is the one-dimensional diffusion of the water molecules formed in the interlayer region by direct condensation of two hydrogen atoms and an oxygen atom. The calculated apparent activation energy of the reaction in the temperature range 620–750 °C is 184 kJ mol⁻¹. The diffusion path is along the axis of the fibrils forming the fibers. The amorphous or short-range ordered dehydroxylate of chrysotile is extremely unstable because forsterite readily nucleates in the Mg-rich regions. Moreover, it is less stable than the dehydroxylate of kaolinite, the so-called metakaolinite, which forms mullite at about 950 °C. This difference is interpreted in terms of the different nature of the two ions Mg²⁺ and Al³⁺ and their function as glass modifier and glass-forming ion, respectively. Received: 10 April 2002 / Accepted: 7 January 2003 Acknowledgements This work is part of a COFIN project (04 Scienze della Terra, NR 17, 2000) supported by MURST. Dr Dapiaggi is kindly acknowledged for help during the data collection at the Dipartimento di Scienze della Terra, University of Milan.