金川超大型铜镍硫化物矿床的铂族元素地球化学特征

对金川超大型铜镍岩浆硫化物矿床岩石、矿石的铂族元素地球化学特征研究表明 ,金川岩体的平均Cu/Pd值远大于原生地幔岩浆的Cu/Pd值 ,说明其岩石为因硫化物析离而失去Pd的岩浆所结晶 ;且岩石的PGE具有部分熔融趋势 ,与地幔橄榄岩接近 ,这些均指示存在岩浆熔离作用。该矿床岩石、矿石的PGE球粒陨石标准化分布模式比较对应 ,均可分为两种类型 ,反映了岩浆多次侵入、熔离分异同时成岩成矿的特征。另外 ,PGE S关系分析表明其成岩成矿过程中有少量地壳物质混染。PGE地球化学特征参数还指示了其高镁拉斑玄武质母岩浆的性质。     

煎茶岭与金川硫化镍矿床的铂族元素地球化学特征对比及其意义

采用ICP—MS方法分析了煎茶岭和金川硫化镍矿床岩石、矿石的铂族元素含量,煎茶岭岩体蛇纹岩的Cu／Pd比值低于原生地幔岩浆,说明岩浆熔离作用较弱,矿石的Pd／Ir比值较小,指示其多数矿石属于岩浆型,以岩浆成矿作用为主;而金川岩体的平均Cu／Pd比值远大于原生地幔岩浆,表明岩浆熔离作用强,矿石的Pd／Ir比值较大,体现了钯族元素矿化及成矿物质以幔源为主的特征。煎茶岭在成矿过程中有壳源物质的混染,整体上岩石、矿石铂族元素含量较低,这与岩浆熔离作用弱、铂族元素成矿作用不发育等因素有关;金川在成岩成矿过程中也有少量地壳物质的混染,但岩石、矿石铂族元素含量较高,反映了以岩浆深部熔离成矿作用为主的特征。     

巯基棉富集-光度法连续测定铬铁矿中的铂钯

在建立巯基棉富集-分光光度法联用系统的基础上,对螯合反应的pH、吸附酸度、显示剂用量、显色温度及体系稳定性等进行了优化选择,并将联用系统成功地应用于实际样品的富集分离分析。在盐酸介质中,α-呋喃二肟与钯得黄色络合物,于λmax=380nm处测定其吸光度,HSCT与铂反应生成2：1稳定络合物,于λmax=540nm处测定其吸光度,对Pt,Pd的检测限（3）分别为0．01μg／ml,0．005μg／ml,对国家一级标准物质进行验证,结果与标准值相符,加标回收率98．0％～102．5％,相对标准偏差为3．88％～8．97％。应用于实际样品的测定．结果满意。     

金川镍铜铂硫化物矿床矿石成因——来自铂族元素地球化学的证据

对金川镍铜铂硫化物矿床Ⅰ、Ⅱ矿区主矿体典型钻孔中的不同类型矿石进行了系统观察和铂族元素分布特征研究。金川矿床中星点状矿石、网状矿石、块状矿石PGE 总量依次降低,由西至东24 号、1 号、2 号矿体的PGE 总量亦具渐次降低趋势。形成块状矿石的硫化物熔体PGE 分异作用较星点状和网状矿石更充分; 块状矿石铂族元素分布特征显示其受晚期硫化物熔体分离结晶和单硫化物固溶体( MSS) 分离作用控制。研究结果表明: 星点状矿石是岩浆分离结晶过程中较快速度冷凝和就地硫化物熔离的结果; 而网状矿石可能是硫化物熔体经深部熔离但未经充分的硫化物分离结晶作用贯入的产物; 块状矿石成因定量模拟结果排除了R 因子控制作用,不同矿体中块状矿石由不同程度的单硫化物固溶体( MSS) 分离结晶所形成。     

混合吸附剂分离富集-电感耦合等离子体质谱法测定地质样品中铂钯金

贵金属分析应用火试金法分离富集时,试金配料复杂、耗时较长,分析成本相对较高,空白较难控制.本文建立了采用过氧化氢-盐酸湿法分解样品,电感耦合等离子体质谱同时测定地质样品中Pt、Pd、Au的分析方法.在10％的盐酸介质中,以LSC-400巯基树脂和活性炭为混合吸附剂,采用动态吸附方式对样品中的Pt、Pd、Au分离富集,用Lu作内标元素,195 Pt、197 Au、108 Pd为待测同位素消除了非谱线干扰和谱线干扰,三元素的回收率均大于96.4％.方法检出限(3σ):Pt为0.06 ng/g,Pd为0.08 ng/g,Au为0.12 ng/g,优于火试金等其他分离富集方法的检出限.应用于测定国家标准物质,Pt、Pd、Au的测定结果与标准值相符,12次测定的相对标准偏差均小于16.1％,满足区域地球化学调查样品的分析要求.该方法操作简便、成本低廉,提高了分析速度,有效地降低了测试过程的空白值.     

扫描电镜-X射线能谱仪在丹巴地区铂族矿物物相特征分析中的应用

丹巴地区铜镍硫化物铂族矿床品位低、铂族矿物颗粒细、铂族元素间的类质同象普遍,此类铂族资源的赋存状态研究及矿石的选冶长期以来都是较为棘手的问题。本文采用扫描电镜-X射线能谱仪器组合,对丹巴铜镍硫化物铂族矿床中含量达到1‰的元素进行快速的定性/定量分析,研究了铂族矿物原位的赋存状态和形貌特征。通过扫描电镜观察到该矿床的铂族矿物主要为砷铂矿、锑钯矿、碲锑钯矿,其次以自然铂、硫砷铑矿、硫砷铱矿,呈椭圆状、纺锤状等形式赋存于黄铁矿、磁黄铁矿及蛇纹石中,部分以类质同象的形式存在,极少量的铂与钯元素呈固溶体形式存在。X射线能谱分析表明该矿床中主要的铂族元素为Pt、Pd,其次为Ru、Rh、Ir、Os; 点分析表明砷铂矿中Pt的含量为52.84%,锑钯矿中Pd的含量为45.15%; 线扫描和面扫描分析表明铂族元素主要分布在含铁的硫化物中,Pt、Pd等铂族元素的含量与铁、镍的含量成正相关关系,反映了丹巴地区铂族元素亲铁、亲镍、亲硫的地球化学特征。     

会理菜子园镍矿床方辉橄榄岩铂族元素、Re-Os同位素及其地质意义

四川省会理菜子园红土型镍矿床中出露较多的基性-超基性岩体,文章系统报道了其中3个橄榄岩体的岩石化学、铂族元素及Re-Os同位素地球化学特征.岩石化学均显示为高MgO及高Mg#值,低SiO2、Al2O3、Na2O、K2O特征,计算显示出主要的标准矿物为橄榄石和紫苏辉石(体积百分数＞90％),表明菜子园属镁质方辉橄榄岩.铂族元素总量比世界上大多数地幔橄榄岩低,且Cu/Pd比值大于原始地幔,可能是早期地幔较高部分熔融出的基性岩浆中硫化物的萃取、抽提作用所致.PPGE相对IPGE强烈亏损,与正常蛇绿岩底部的地幔橄榄岩特征类似,向右倾斜的原始地幔标准化配分模式表明菜子园铂族元素体系主要受地幔部分熔融的控制.PPGE中,Pt相对于Pd富集,可能与后期强烈蚀变有关,此外还可能反映了少量Pt以合金形式残留于方辉橄榄岩中,Pd以不相容元素的形式更多被熔体带走.菜子园方辉橄榄岩的Re-Os同位素体系封闭性相对好,γ(Os)值较小.岩石化学、铂族元素及Re-Os同位素地球化学显示,菜子园橄榄岩直接来自地幔,属正常蛇绿岩套底部的方辉橄榄岩,为古小洋盆洋壳的残片.菜子园蛇绿岩反映了中元古代晚期昆阳裂谷在菜子园-踩马水-麻塘断裂带以北演化成小洋盆,于其中沉积会理群,并在中元古代末期与南侧的东川群、汤丹群碰撞、拼贴.菜子园橄榄岩的蛇绿岩属性进一步证明,扬子地台西南缘的基底由不同时代的小陆块碰撞、拼贴导致基底陆壳增生.     

A Comparative Study of Five Reference Materials and the Lombard Meteorite for the Determination of the Platinum‐Group Elements and Gold by LA‐ICP‐MS

A range of independently characterised reference materials (RMs) for LA‐ICP‐MS, used for the determination of the platinum‐group elements (PGE) and Au in a sulfide matrix, were analysed and compared: 8b, PGE‐A, NiS‐3, Po727‐T1, Po724‐T and the Lombard meteorite. The newly developed RM NiS‐3 was used as the RM for the calibration of all LA‐ICP‐MS analyses and the measured concentrations of the other RMs compared against their published concentrations. This data were also used to assess the consistency of concentrations calibrated against the different RMs. It was found that Po727‐T1 and 8b produced results that were comparable, within uncertainty, for all elements. Po727‐T1 also produced consistent results with NiS‐3 for all elements. All other RMs showed differences for some elements, especially Ru in Po724‐T, and Os, Ir and Au in PGE‐A. The homogeneity of the PGE and Au in each RM was assessed, by comparing the precision of multiple LA‐ICP‐MS spot analyses with the average uncertainty of the signal. Po724‐T, Po727‐T1 and the Lombard meteorite were found to be homogeneous for all elements, but 8b, PGE‐A and NiS‐3 were heterogeneous for some elements. This is the first direct comparison between a range of independently characterised PGE and Au LA‐ICP‐MS RMs.     

豆荚状铬铁矿多阶段形成过程的讨论

豆荚状铬铁矿是铬的主要来源,是中国的紧缺矿种,因此,寻找一批大型铬铁矿矿床已成为解决我国对铬铁矿长期依赖进口的途经.然而对于豆荚状铬铁矿的成因,一直以来都有较大分歧.豆荚状铬铁矿及其围岩地幔橄榄岩中大量异常地幔矿物的发现,引起了各国地质学家对豆荚状铬铁矿成因的新一轮思考.本文着重讨论近年来国内外学者对豆荚状铬铁矿研究的最新成果和进展,包括豆荚状铬铁矿的形态特征、产出规律、矿物化学、铂族元素(PGE)的分布模式,铬铁矿矿石中出现的超高压矿物,以及围岩地幔橄榄岩的演化过程等等.豆荚状铬铁矿中的铬来源于两种辉石的不一致熔融与副矿物铬尖晶石,其形成环境可能在下地幔或者是过渡带的位置.豆荚状中含铂族元素矿物呈包裹体状和裂隙状分布,铂族元素含量与铬铁矿形成过程中的S饱和程度有关,具有多期性的特征.进而初步地拟定了豆荚状铬铁矿形成过程存在四个阶段,分别为铬的来源阶段、铬尖晶石及超高压矿物的结晶阶段、铬铁矿的成矿阶段、铬铁矿的就位阶段,而每一阶段的特征还需进一步细化与翔实,并且需要对不同岩体不同产出的豆荚状铬铁矿矿床进行详细的对比研究.     

Experimental Study of Gold and Platinum Solubility in a Complex Fluid under Hydrothermal Conditions

Abstract: The solubility of gold was studied in water and aqueous NaCl (1– 5 m) solutions under oxygen and sulfur buffered conditions between 300–500C at a constant pressure 1 kb. Two buffer assemblages HMP and PPM were used. Analysis of the scatter in measured values in log m_Au–m_NaCl–T frame fixed linear dependence between log m_Au and T at any studied iso‐pleth (m_NaCl) in the form of log m_Au = a. T(C) + b. Coefficients of the equation were calculated for water and NaCl (1, 3, 5 m) solutions. The maximum solubility characterizes the NaCl‐free system in the presence of HMP. In the case, Au solubility increases from (log m_Au) –6. 72 to –5. 04 at 300 and 500C, respectively. In the presence of PPM, maximum of Au solubility was obtained for the 5 mNaCl solution. In a similar manner solubility rises from –6. 54 to –5. 77 at 300 and 500C, accordingly. In studied f_O2/f_S2 area the behavior of Au solubility testified that: (i) – a composite interaction between chloride and hydrosulfide speciation of gold affects its total solubility; (ii) – in addition of NaCl up to about 1. 5 m the solubility decreases, more pronounced in the presence of HMP; (iii) – the contribution of chloride in total Au solubility is more for PPM despite of lower f_O2value, than for HMP. The solubility of platinum was studied in the Pt–Cl–S–H₂O system between 300 and 500C, 1 kb. PPM solid buffer controlled oxidation state, pH and sulfur activity of solutions (H₂O, 1 mNaCl and 0. 1 mHCl). Under the conditions, PtS precipitated from the solutions with increasing temperature and acidity. The PtS solubility in the 0. 1 m_HCl solutions lowers slightly in the range of 300–500C from –5. 30 to –5. 60 (in log m_Pt) that is typical to the hydrosulfide species. It was deduced that reducing media, regulated by the PPM assemblage, suppress activity of chloride species of Pt. More oxidizing conditions were modeled in runs using mixtures of Mn(II), Mn(III) and Mn(IV) oxides to buffer the aqueous‐chloride solutions between 300 and 500C, 1 kb. It was found that MnO tends to oxidize at T below 400C forming intermediate Mn‐hydroxides (β–MnOOH, Mn (OH)₂ and Mn₂(OH)₃Cl). These phases are metastable and transfer to Mn₃O₄ with increasing duration. Generation of the Mn‐hydroxides leads to a change of physical‐chemical parameters of the solutions, such as water activity, pH and Eh. The last results in abrupt increase in the noble metals dissolution. At stable existence of only Mn₃O₄, the solubility of both Pt and Au lowers to equilibrium values. Essential catalysis effect of Pt on intensity and rate of Mn(II) oxidation was found. The dominant role of chloride of Pt and Au was defined under most oxidized conditions, specified by Mn₂O₃–MnO₂ buffer. So at 400C, dissolved Au (log m_Au) increases from –4. 40 in water to –1. 00 in 0. 1 m_HCl, and ones of Pt (log m_Pt) from –4. 80 to –2. 90 accordingly. Thus, mixing of hydrosulfide and chloride solutions, as well as transformation of the systems to the stable state act upon total solubility of the noble metals.