溶浸工艺中水分运移实验研究

实验研究铜矿在一定喷淋强度下溶浸时水分运移的基本规律。实验表明，矿柱的喷淋过程是一个矿物颗粒吸湿．颗粒之间的孔隙则是一个逐渐由非饱和转化为饱和的过程。只要适当地控制好喷淋强度，就能使矿柱或矿堆保持长时间的非饱和状态，有利于有用元素的浸出。对于溶浸而言，需要保持矿柱较长时间的非饱和状态。因此，喷淋强度选择小的值的比较好，从实验结果可以看出，对于该实验所选取的矿柱，控制喷淋强度在1．243E～2cm／min和5．238E～2cm／min比较合理。     

新疆哈尔里克山二叠纪碱性花岗岩-石英正长岩组合的成因及其构造意义

哈尔里克奥姆尔塔格碱性花岗岩(OMAG)侵入于小铺东二长花岗岩中.该岩体岩性较均一,呈灰紫色,主要矿物组合为石英、钾长石、钠长石、碱性角闪石和霓石;化学成分上富硅、碱,贫钙、镁,低铝;富Rb、Th、U和Zr,Ga/AI比值大(3.18×10~4～3.56×10~4),贫Ba、Sr,岩石中Co、Cr、V和Ni等过渡元素显著亏损,U、Hf、Zr和Nb等高场强元素的含量高;稀土总量较高,配分模式右倾,并具有显著的负铕异常;LA-ICP-MS锆石~(206)Pb/~(238)U加权平均年龄为287.6±2.1Ma;具有正的ε_(Nd)(t)值(+4.96),较低的(~(87)>Sr/~(86)Sr);值(0.70159).同样侵入于小铺东二长花岗岩中的恰干昆多沟含角闪石石英正长岩(QGQS)也呈灰紫色,其结构和构造与OMAG非常相似.两个岩体在主量元素和REE图解上均呈现有规律的分布和一致的演化趋势.从QGQS到OMAG,SiO_2含量增加(从64.71%～64.83%到71.23%～74.31%)、全碱含量降低(从11.72%～11.79%到8.49%～9.87%)和Al_2O_3含量减少(从16.09%～16.19%到11.44%～13.34%)、稀土总量减少(从592.3×10~(-6)～656.0×10~(-6)到273.9×10~(-6)～405.9×10~(-6))、轻/重稀土比值降低(从18.2～20.1到4.4～6.0)、稀土配分曲线从平滑到Eu显著亏损.基于OMAG的岩相学、矿物学、地球化学、锆石年代学和与QGQS的对比研究,笔者认为奥姆尔塔格碱性花岗岩可能是由石英正长岩母岩浆经过分离结晶作用演化的产物,且这种石英正长岩岩浆起源于亏损地幔;根据哈尔里克造山带地质演化历史的分析,这两个岩体均形成于紧随主碰撞后的挤压-伸展转折阶段.     

国内外寻找隐伏矿化探新方法研究进展

简要总结了根据超显微镜物质的迁移吸附机制和矿物结构与成矿物关系寻找隐伏矿的化探新方法的原理,技术及试验应用效果,预计这些方法技术近期内在寻找隐伏矿及解决环境,地震预报,地热工发等研究领域发挥重要作用。     

杂卤石矿地浸模拟实验研究

通过对难溶含钾矿物杂卤石的柱浸实验模拟石溶浸过程分析发现,采用CaCl2溶液作溶浸剂,其溶浸剂浓度、淋洗速度、矿石粒度、浸滤路径等因素对K溶浸率及溶浸速度均有影响,当矿石粒度为1 mm和5 mm时,钾浸出率分别可达到80%和70%以上,溶浸剂浓度增加,可提高钾的浸出率,但CaCl2浓度高于5%后,效果不明显。淋洗速度增大,虽可提高钾的浸出率,但同时浸出液中钾的富集程度有所降低,以4.5 ml/h～10 ml/h为佳;增加渗滤路径长度可同时提高钾的浸出率和富集程度。实验结果表明杂卤石溶解过程受固相层扩散控制,溶解反应过程较好地符合“收缩未反应核模型”的固相控制动力学方程1-(2/3)α(1-α)2/3=(2MD′c/bργ02)t。研究结果为地浸开采深埋藏杂卤石提供了一定的实验基础。     

柴达木盆地冷湖地区古近——新近系可地浸砂岩型铀矿成矿前景

从地质、水文地质两个方面入手,分析了柴达木盆地冷湖地区古近—新近系有利于可地浸砂岩型铀矿成矿的铀源,泥—砂—泥结构,补—径—排条件,及不利于可地浸砂岩型铀矿成矿与开发的构造因素。     

华北克拉通南缘张士英岩体大陆动力学背景:来自地球化学、锆石U-Pb年龄和Hf同位素的证据

张士英岩体位于华北克拉通南缘,岩体主要由石英正长岩组成。石英正长岩的LA-ICP-MS锆石U-Pb年龄为122.8±1.5Ma。其Si O2含量为66.04%~67.80%,Na2O+K2O=9.03%~10.97%,K2O=4.40%~6.37%,K2O/Na2O1属于钾质长英质岩石。A/CNK=1.26~1.58,A/NK=1.63~1.79属于过铝质岩石系列。石英正长岩的Mg#变化范围在12.9~39.4。富集LREE亏损HREE,轻重稀土分异明显,(La/Yb)N=15.48~21.12,Eu呈弱的负异常(δEu=0.54~0.99)。富集Rb、K、Th、U等大离子亲石元素,亏损Nb、Ta、P、Ti等高场强元素。张士英石英正长岩岩浆锆石εHf(t)集中在-17.6~-13.9,Hf两阶段模式年龄tDM2集中在1.7~1.9Ga。石英正长岩的岩浆Zr饱和温度高(936~998℃)。地球化学及同位素显示张士英石英正长岩源区主要为古老的壳源物质,并有少量年轻组分加入,这种年轻组分是幔源物质。岩体形成于拉张性构造环境下,拉张性的环境导致了幔源物质的上涌,底侵下地壳使其发生部分熔融。形成时代正好位于华北克拉通破坏峰期,张士英石英正长岩正是这一地质事件的响应。     

矿产品中污染物溶解释放研究进展

我国原矿、精矿消费量和尾矿产出量巨大,这些矿产品中有毒有害污染物的溶解释放(称为"溶出")已经成为一个普遍存在的环境问题。本文阐述了目前国内外矿产品污染物溶出的研究现状,总结了研究矿产品中污染物溶出最常用的四种模拟试验方法(湿度室试验、淋滤柱试验、静态浸泡试验、萃取试验)的应用进展。湿度室试验可模拟自然风化过程,确定污染物溶出速率和产物;淋滤柱试验可模拟降水和喷淋过程,提供污染物吸附和解吸附动力学依据;静态浸泡试验可模拟被水浸泡过程,探明溶出规律和产物;萃取试验可对污染物进行形态分析,评估介质中污染物的流动性、稳定性等。污染物溶出的各种影响因素由强到弱依次是pH值、淋溶浸泡时间、温度、固液比、矿石粒径,多数情况下pH值越大、浸泡时间越长、温度越高、固液比越小、粒径越小越有利于污染物的溶出。溶出是一个长期和具有潜伏性的过程,其内部发生一系列物理化学反应,显示出与扩散效应不同的规律。目前这方面的研究对象还主要集中于废弃的尾矿,对经运输、堆放并在人类生活区使用的原矿、精矿产品的污染物溶出有待进一步研究,需要对其溶出污染进行预测和评估,采取有效措施控制和治理矿产品的污染。     

黝铜矿-砷黝铜矿矿物学研究进展

黝铜矿-砷黝铜矿系列矿物(Tetrahedrite -Tennantite Series Mineral,TTSM)作为含Cu、Ag、S、Sb、As、Hg及少量Au、Fe、Zn、Cd、Bi、Te、Se的硫盐矿物广泛存在于世界各地的Cu、Ag、Au、Pb、Zn多金属矿床中.为了能够更好的认识该系列矿物,提高矿物中有用元素的回收率,扩大黝铜矿型铜矿床的经济效益,本文对TTSM的化学组成和类质同象置换规律,晶胞参数和晶体结构的形变,矿物人工合成和有用元素的浸出试验等研究进展进行了综述.天然TTSM矿物一般化学式为:(Cu,Ag)6 Cu4 (Fe,Zn,Cu,Hg,Ag,Cd)2 (Sb,As,Bi,Te)4 (S,Se)13,其中S-Se、Sb-As-Bi-Te、Ag-Cu、Cu-Hg-Fe-Pb-Zn-Cd的类质同象置换相当普遍;TTSM晶体结构中不同结构位置离子置换规律更多的受限于离子价键,而同一结构位置不同离子的置换除受限于离子价键还受限于该位置空间大小,晶胞参数与离子置换类型和数量密切相关;人工合成实验证实形成TTSM矿物的温度范围为350～540℃,浸出试验证明随反应温度增高、浸出浓度增大、矿物颗粒减小时,TTSM中有用元素的浸出速率增大.     

Pervasive assimilation of carbonate and silicate rocks in the Hortavær igneous complex, north-central Norway

The intrusive complex at Hortavær represents a magma transfer zone in which multiple pulses of gabbroic and dioritic magmas evolved along Fe- and alkali-enrichment trends. Extreme alkali enrichment resulted in nepheline-normative and sparse nepheline-bearing monzodioritic and monzonitic rocks. More evolved monzonitic and syenitic rocks are silica saturated and, in some cases, quartz bearing. Previous and current research recognized an abundance of clinopyroxene and other Ca-rich phases, such as scapolite, grossular-rich garnet, and igneous-textured calcite among the mafic and intermediate rocks. Even the most pyroxene-rich samples contain low Sc concentrations, which suggests early, intense fractionation of clinopyroxene. These features and the alkali enrichment are consistent with assimilation of carbonate-rich host rocks. Carbon isotope ratios of the igneous-textured calcite indicate an origin of the carbon from host rocks rich in calcite, consistent with assimilation. However, low _Nd values (−3.4 to −10.2) and moderate initial ⁸⁷Sr/⁸⁶Sr values (0.7052 to 0.7099) indicate the need for assimilation of quartzofeldspathic rocks as well. Models of combined assimilation and fractional crystallization indicate that assimilation of simple end members, either carbonate or silicate, cannot explain the entire data set. Instead, variable proportions of carbonate and silicate materials were assimilated, with the most pronounced assimilation effects in the mafic rocks. The reasons for variable degrees of assimilation are, as yet, uncertain. It is possible that assimilation of calc-silicate rocks with variable carbonate/silicate proportions resulted in the range of observed compositions. However, the importance of carbonate assimilation in mafic rocks compared to felsic ones suggests that assimilation of carbonates was predominant at high temperature and/or mafic magma compositions and assimilation of silicates was predominant at lower temperature and/or felsic magma compositions. We suggest that the ability of the mafic magma to dissolve higher proportions of carbonate contaminants is the result of the magma's ability to form clinopyroxene as a product of assimilation. In any case, extensive carbonate assimilation was possible because CO₂ escaped from the system.     

Pyrite Oxidation in Leaching Process of Radionuclides and Heavy Metals from Uranium Mill Tailings

Pyrite is a sensitive mineral in the geological environment,and its oxidation produces an important geochemical and environmental effect on the control of the redox and pH conditions.Column experiment results were used for modeling the geochemical processes in uranium mill tailings under leac-hing conditions.Oxidation of pyrite dominates the control of the tailings leaching process.The experi-mental and modeling results show that the leachate chemistry changes substantially with the decrease in pyrite consumption.In the initial stage of the leaching experiment,the pyrite is consumed several hun-dred times grater than that in the later stages,for much more oxygen is present in the tailings in the ini-tial stage.As the experiment continues,the tailings is gradually saturated with water and the oxygen concentration greatly decreases and so does pyrite consumption.The experimental and modeling results are useful for the design of mill tailing decommissioning:oxidation process and transport of radioactive nuclides and heavy metals can be constrained by controlling the oxygen concentration of tailings and the infiltration of meteoric water.