福建省上杭-大田地区中生代成岩成矿作用与构造环境演化

本文所研究的四个中生代花岗岩体具不同的同位素年代:汤泉岩体为183～158Ma,紫金山岩体为157-145Ma。才溪岩体为133Ma,四方岩体为108～105Ma,汤泉和紫金山岩体分别属于早中生代中、晚侏罗世,才溪和四方岩体时代为晚中生代早白垩世。汤泉和四方岩体为A/CNK<1.0的准铝质花岗岩类,因富Ba、Sr,贫HREE、Y、Yb而具埃达克岩地球化学特征,是最具铜矿成矿潜力的含矿母岩;紫金山花岗岩体为A/CNK>1.1的强过铝花岗岩,并富K、Rb、Th、Y、HREE,贫Sr、Ba、Ti,具地壳泥质岩石熔融的特征。才溪岩体为A/CNK1.0～1.1的弱过铝花岗岩,其元素地球化学特征介于四方岩体和紫金山岩体之间。富Na2O的汤泉岩体是地幔起源的基性岩浆底侵作用,促使加厚的元古代下地壳基性岩石部分熔融所形成,是铜、铁多金属矿床成矿系列的主要含矿母岩;富K2O的四方岩体是地幔起源的富钾基性岩浆与中下地壳物质部分熔融形成的花岗质混合岩浆,使岩浆中的K2O含量增高,并从地幔中获取大量铜及其它金属和硫,而成为斑岩型铜金多金属矿床成矿系列的主要含矿母岩。研究区自早-中侏罗世(180Ma)以来已有岩石圈伸展的岩石学记录。紫金山强过铝花岗岩是这种伸展机制延续的结果。随时间推移,岩石圈伸展减薄作用和底侵作用增强,地幔组分在花岗质岩浆的形成过程中贡献     

金属矿物材料在废水处理中的应用

从环境矿物学角度，对金属矿物材料(铁氧化物与氢氧化物、锰氧化物和氢氧化物、铁硫化物)在废水处理中的应用现状进行了综述，分析金属矿物材料在水环境保护方面存在的问题，并对其应用前景进行展望。     

New Thorium Isotope Ratio Measurements in Silicate Reference Materials: A‐THO,AGV‐2, BCR‐2, BE‐N,BHVO‐2 and BIR‐1

A two‐step Th isolation protocol, involving micro‐columns of TRU‐Spec extraction chromatography material and AG1 resin, was evaluated. The MC‐ICP‐MS procedure included ²³²Th tailing characterisation and correction, and calibrator bracketing using an in‐house standard solution (ThS1) to correct for instrumental mass bias and Faraday cup to secondary electron multiplier relative gain. Repeated analyses of reference solutions (UCSC Th ‘A’, WUN, OU Th ‘U’, IRMM‐36) were consistent with published data. Six reference materials (A‐THO, BCR‐2, AGV‐2, BHVO‐2, BE‐N and BIR‐1) were processed. The average ²³⁰Th/²³²Th values obtained for these samples are in excellent agreement with published data. In addition, we report the first ²³⁰Th/²³²Th values for BE‐N and BIR‐1. The intermediate precisions for rock samples ranged from ± 0.24 to ± 0.49% (2 RSD) and were similar to those achieved for synthetic solutions, thereby supporting the overall validity of the chemical separation, data acquisition and reduction procedures. Counting statistics on the ²³⁰Th isotope was the most significant source of uncertainty. The intermediate precision of the mean ²³⁰Th/²³²Th for the Th‐depleted BIR‐1 (5.64 × 10^?6 ± 0.27%, 2 RSD) is in the range of the analyses of other reference materials analysed in this study.     

羟基铝镍多孔粘土材料的表面酸性及其孔容

把羟基铝镍聚合物引入蒙脱石层间,制备多孔粘土材料,利用XRD、IR及非水溶液滴定法研究了制备方法及条件变化对材料表面酸性及孔容的影响。结果表明,制备方法及Al／Ni、(Al Ni)／土、老化温度等条件对表面酸性及孔容均有影响,材料在400℃以下热稳定性较好。     

An Evaluation of Methods for the Chemical Decomposition of Geological Materials for Trace Element Determination using ICP-MS

Complete dissolution is essential to obtain accurate analytical results using ICP-MS. In this study, decomposition techniques (i.e. acid digestions using Savillex Teflon vials, a high pressure digestion system and microwave oven, a combined lithium tetraborate fusion - HF/HNO3 acid decomposition and sodium peroxide sinter) for the total dissolution of different types of geological reference materials have been investigated. Savillex Teflon vial HF/HNO3 digestion is effective for basaltic samples. The high pressure HF/HClO4 digestion (PicoTrace TC-805 digestion system, Bovenden, Germany) allows dissolution of basalts and ironstones. Granites and magnetite-rich samples can be dissolved using a high pressure HF/H₂SO₄ method. Geological samples cannot be effectively attacked by microwave acid digestion. A combined lithium tetraborate fusion - HF/HNO3 acid digestion method allows complete dissolution of many different types of geological materials; however, this method precludes the determination of volatile elements due to the high fusion temperature (1000 °C). A sodium peroxide sinter method at 480 °C has the potential for the rapid determination of Y, Sc and REE in different types of geological materials. However, the lack of ultra-pure reagents precludes the use of lithium tetraborate fusion and sodium peroxide sinter methods for the measurement of geological samples with low trace element abundances.     

Determination of Chlorine in Nine Rock Reference Materials by Isotope Dilution Mass Spectrometry

A procedure for the determination of chlorine by the isotope dilution technique (ID) using negative thermal ionisation mass spectrometry (N-TIMS) is described. Silicate samples of about 10 mg were spiked and decomposed with hydrofluoric acid, and chlorine was isolated by precipitation of silver chloride after neutralisation with Ca(OH)₂. The ammonical solution of AgCl was then subjected to N-TIMS. Replicate analyses of rock reference materials, typically of JB-1 and JR-1, demonstrated the high quality of the analyses (precision for Cl was ± 1-2%). We present here the most precise data sets of chlorine concentrations in nine igneous rock reference materials, three basalts (JB-1, JB-2, JB-3), two andesites (JA-3, AGV-1), two rhyolites (JR-1, JR-2) and two granodiorites (JG-3, GSP-1). The chlorine concentrations found ranged from 152 μg g-1 in AGV-1 to 1008 μg g^-1 in JR-1. Our results presented here are partly (but not completely) in agreement with recommended values, where they are available. The N-TIMS ID technique can thus be used as a means of determining low chlorine contents in silicate materials to high precision.     

大龙山岩体和城山岩体的铅同位素组成特征及其成因探讨

详细研究了大龙山岩体和城山岩体钾长石的铅同位素组成,并参考这些岩体的黑云母化学成分、锶同位素、稀土元素、岩石化学和地球物理资料,发现它们是多阶段侵入的复式岩体,与庐枞火山岩系有渊源关系,属燕山晚期岩浆活动的产物。它们的初始成岩物质来源于上地幔部分熔融,岩浆上升侵位过程中已不同程度地受到了上部地壳的混染。经计算,其中约有61.6％的铅来自上地幔,约有38.4％铅来自上地壳,该区陆壳的乎均年龄约26亿年,陆壳在演化过程中具有富铀的趋势。这些岩体与深大断裂和地幔隆起有成因上的密切联系。     

Determination of Reference Values for NIST SRM 610–617 Glasses Following ISO Guidelines

We present new reference values for the NIST SRM 610–617 glasses following ISO guidelines and the International Association of Geoanalysts’ protocol. Uncertainties at the 95% confidence level (CL) have been determined for bulk‐ and micro‐analytical purposes. In contrast to former compilation procedures, this approach delivers data that consider present‐day requirements of data quality. New analytical data and the nearly complete data set of the GeoReM database were used for this study. Data quality was checked by the application of the Horwitz function and by a careful investigation of analytical procedures. We have determined quantitatively possible element inhomogeneities using different test portion masses of 1, 0.1 and 0.02 μg. Although avoiding the rim region of the glass wafers, we found moderate inhomogeneities of several chalcophile/siderophile elements and gross inhomogeneities of Ni, Se, Pd and Pt at small test portion masses. The extent of inhomogeneity was included in the determination of uncertainties. While the new reference values agree with the NIST certified values with the one exception of Mn in SRM 610, they typically differ by as much as 10% from the Pearce et al. (1997) values in current use. In a few cases (P, S, Cl, Ta, Re) the discrepancies are even higher.     

The C-O and Zn isotopic compositions of the Laochang Ag-Pb-Zn ore bodies in the Changning-Menglian suture zone,and its geological implicationsSCIEI北大核心CSCD

老厂矿床是昌宁-孟连缝合带内唯一大型矿床,本文报道了老厂矿床Ag-Pb-Zn矿体中Ⅰ号矿体群下部块状矿体和上部网脉状矿体的方解石C-O同位素组成,以及Ⅰ、Ⅱ、Ⅳ三个矿体群内闪锌矿的Zn同位素组成。Ⅰ号矿体群下部块状矿体和上部网脉状矿体方解石δ¹³C_PDB的范围分别为-6.17‰～2.71‰和-2.18‰～3.87‰,δ¹⁸O_PDB的范围分别为-19.57‰～-17.23‰和-22.10‰～-16.21‰;计算获得对应成矿流体的δ¹³C_CO2为-6.16‰～1.53‰和-2.39‰～6.43‰,δ¹⁸O_H2O分别为1.62‰～7.62‰和4.36‰～16.92‰,通过与岩浆CO₂(δ¹³C=-2‰～-8‰)和围岩灰岩(δ¹³C=-1.6‰～4.0‰)的δ¹³C值相比较,指示块状矿体成矿流体中的碳主要来自岩浆,网脉状矿体成矿流体中...     

易破碎粒状材料本构研究

粒状材料被广泛地应用到土木工程的各个领域。大部分粒状材料在外力作用下较容易产生颗粒破碎,颗粒破碎对材料的力学性能有很大的影响。为了更好地描述易破碎粒状材料的力学特性,基于弹塑性力学和临界状态土力学开发了一种能够考虑颗粒破碎效应的本构模型。此本构模型能够考虑在剪应力和压应力作用下引起的颗粒破碎对粒状材料力学性能的影响。为了考虑颗粒破碎的影响,基于对Cambria 砂的高压试验,得出了临界状态线位置与消耗塑性功之间的关系,并称之为“破碎方程”。此本构模型拥有双屈服面,分别考虑剪切和等向压缩产生的塑性变形。通过试验结果与数值计算结果的对比得出,新的本构模型能较好地描述易破碎粒状材料的力学特性