高铝粉煤灰中部分主微量元素的分布规律研究

本文旨在研究部分主微量元素在高铝粉煤灰中的分布规律,从而为其资源化利用提供科学依据。首先根据高铝粉煤灰的物相组成特点采用新的分离方法将之分离为三个相(或相组合):铁质微珠、莫来石-刚玉相以及玻璃相;然后分别用化学分析和ICP-MS测试主微量元素在高铝粉煤灰、铁质微珠以及莫来石-刚玉相中的含量,并结合相关数据计算出这些元素在玻璃相中的含量。结果表明,除Al、Mn外,其他元素均在玻璃相中有不同程度的富集;除Al外,其他元素则在莫来石-刚玉相中有不同程度的贫化;除Ti以外的铁族元素以及除Ga、Pb以外的金属成矿元素均在铁质微珠中富集,其他元素则在其中贫化。     

Report (1967–1981) on Four ANRT Rock Reference Samples: Diorite DR-N, Serpentine UB-N, Bauxite BX-N and Disthene DT-N

All data reported by 200 analysts (106 laboratories) are presented for the four ANRT samples: Diorite DR-N, Serpentine UB-N, Bauxite BX-N and Disthène DT-N. Recommended values are given for the major and minor elements. As far as the as trace elements are concerned, DR-N has been characterized for 35 elements whereas the other three samples have been for only 20 elements. Wherever possible, brief comments have been inserted so as to explain our way of assigning recommended or proposed values.
After more than a decade of existence the total number of data reported for all the four samples reach only 3200 units which are not sufficient enough for a valid evaluation of compiled data. It is also pointed out that these samples are most likely to be available even during the next century as they have been prepared in large quantities of the order of one ton. A plea is therefore made for contribution of more data particularly for trace elements and for major elements which are present as trace elements in UB-N, BX-N and DT-N.     

Signatures of Holocene Hydrological Processes from Sedimentary Archives in Southwestern India: Case Studies from Wetlands of Kerala Coast

This study investigates the abundance, modes of occurrence and origin of major and trace elements in the Jurassic Tazareh coal in the northern Iran. A total of 27 samples (coal, coaly shale and siltstones) were collected and analyzed for trace elements by neutron activation analysis (INAA) and for major elements by X-ray fluorescence. The abundance of these elements is discussed in relation to local geological conditions. The correlation between the various elements is demonstrated through scatter diagrams and the possible genetic associations are discussed. Most elements (Al, Si, Na, K, Fe, Mg, Ti, Ba, Cr and REE) are positively correlated with ash yields that are inorganically associated. Bromine displays statistically signiûcant negative correlations with ash yield. The Ca, Zn, Se, As and Co present mixed modes of occurrence in the coal and probably associate with organic fraction.     

Inter-element relationships between trace elements in primitive carbonaceous and unequilibrated ordinary chondrites

The results of a search for significant (95 % confidence level) inter-element relationships among 13 trace elements in carbonaceous chondrites and 26 elements and the disequilibrium parameter for silicate phases in unequilibrated ordinary chondrites (UOC) indicate pronounced differences in the formation processes of these two sorts of primitive chondrites. Twenty-six pairs of elements are correlated in carbonaceous chondrites and these correlations lend support to a model involving mixing in different ratios of material differing in thermal history.Comparison of the 26 elements in UOC shows that 39 pairs of elements are significantly related and only very volatile elements are correlated with the disequilibrium parameter. Each of the inter-element relationships can be specifically ascribed to a metal-silicate fractionation in the solar nebula or to a thermal fractionation. These relationships are about equally consistent with the metamorphism, two-component condensation and simultaneous accretion-condensation models for the origin, of the ordinary chondrites, each requiring adoption of specific ad hoc assumptions for complete consistency.     

热液型金矿床围岩蚀变过程中元素迁移规律--以张家口地区东坪、后沟、水晶屯金矿为例

张家口地区东坪、后沟、水晶屯金矿围岩蚀变发育 ,主要的蚀变类型有钾长石化、硅化、黄铁矿化、绿泥石化等。通过蚀变岩常量元素、微量元素的定量计算发现 ,三个金矿床围岩蚀变过程中元素迁移、富集有明显的规律 ,即常量元素 (SiO2 、K2 O、FeO) ,亲硫元素 (成矿元素 :Au、Ag、As、Sb、Bi、Pb、Zn)明显富集 ,其它亲铜亲铁元素 (Cr、Co、Ni、Cu)略有富集。蚀变热液是一种来自深部的携带亲硫元素富硅的碱性流体     

Mass Fractions of Forty‐Six Major and Trace Elements,Including Rare Earth Elements,in Sediment and Soil Reference Materials Used in Environmental Studies

Development of new techniques, enabling simultaneous determination of large numbers of elements in environmental samples, can force analysts to use certified reference materials that do not contain all the elements of interest. In this paper, the mass fractions of forty‐six major and trace elements, including rare earth elements (REE), are presented in one soil (NCS DC 77302 also known as GBW 07410) and five sediment (Metranal‐1, IAEA 405, MESS‐3, NCS DC 73309 also known as GBW 07311 and NCS DC 75301 also known as GBW 07314) certified reference materials determined by high resolution inductively coupled plasma‐mass spectrometry. The selected certified materials represent a spectrum of geological matrices often analysed in environmental studies. Measured elements include certified elements, elements listed with information values as well as new elements absent from certificates, including REEs and some other elements. REE + Y mass fractions in the river sediment reference material Metranal‐1 are reported for the first time. The results obtained are in agreement with available certified or information values.     

江西德兴斑岩铜矿床某些元素的扩散和渗滤作用

以江西德兴斑岩铜矿床之细矿脉为研究对象,文章介绍了细矿脉剖面采集及研究的工作方法,着重讨论了自矿脉至围岩元素的空间展布特征。成矿元素Cu、Ag、S和控矿元素Fe、Rb、K都属确定性分布型。对照元素的扩散和渗滤理想模式,得到如下认识:在成矿成晕的地球化学过程中,成矿元素Cu、Ag、S以及Fe以扩散作用为主,控矿元素K和Rb以渗滤作用为主。     

Geochemistry of environmentally sensitive trace elements in Permian coals from the Huainan coalfield, Anhui, China

To study the geochemical characteristics of 11 environmentally sensitive trace elements in the coals of the Permian Period from the Huainan coalfield, Anhui province, China, borehole samples of 336 coals, two partings, and four roof and floor mudstones were collected from mineable coal seams. Major elements and selected trace elements were determined by inductively coupled plasma optical emission spectrometry (ICP-OES), inductively coupled plasma mass spectrometry (ICP-MS), and hydride generation atomic absorption spectrometry (HAAS). The depositional environment, abundances, distribution, and modes of occurrence of trace elements were investigated. Results show that clay and carbonate minerals are the principal inorganic constituents in the coals. A lower deltaic plain, where fluvial channel systems developed successively, was the likely depositional environment of the Permian coals in the Huainan coalfield. All major elements have wider variation ranges than those of Chinese coals except for Mg and Fe. The contents of Cr, Co, Ni, and Se are higher than their averages for Chinese coals and world coals. Vertical variations of trace elements in different formations are not significant except for B and Ba. Certain roof and partings are distinctly higher in trace elements than underlying coal bench samples. The modes of occurrence of trace elements vary in different coal seams as a result of different coal-forming environments. Vanadium, Cr, and Th are associated with aluminosilicate minerals, Ba with carbonate minerals, and Cu, Zn, As, Se, and Pb mainly with sulfide minerals.     

云南镇沅金矿煌斑岩的蚀变流体特征

云南镇沅金矿煌斑岩的蚀变流体特征黄智龙，王联魁，朱成明’（中国科学院地球化学研究所，贵阳５５０００２）（中国科学院广州地球化学研究所，广州５１０６４０）关键词云南镇沅，煌斑岩，蚀交流体，元素迁移煌斑岩为易受蚀变的一种岩石，国外报道的许多能代表原生岩浆...     

云南镇沅金矿煌斑岩蚀变过程中元素活动规律

广泛分布于云南镇沅金矿、与金矿化在时间上、空间上密切共生的煌斑岩普遍遭受不同程度的蚀变。根据岩石的蚀变相对强弱，本区煌斑岩可分成新鲜（弱蚀变）、蚀变两种。质量平衡方程对蚀变过程中元素活动规律的计算结果表明，引起本区煌斑岩蚀变的流体为一种含过渡元素、亲石元素、挥发性元素和亲硫元素（或成矿元素）的富硅、铝碱性流体，这种流体可能是本区煌斑岩岩浆演化到晚期分异出来的产物。关键词     

喜马拉雅淡色花岗岩——关键金属Sn-Cs-Tl的富集机制

关键金属是全球高科技产业不可或缺的战略性资源,其富集机制和成矿作用是目前国际矿床学研究的热点之一。我们对喜马拉雅带吉隆和亚东地区淡色花岗岩开展系统的地球化学研究,发现侵入到藏南拆离系的淡色花岗岩含有较高的Sn、Cs、Tl、Be、W、B、Li和Bi。全岩元素地球化学分析表明,这些淡色花岗岩具有如下特征：（1）富集关键金属元素;（2）为原始岩浆经历斜长石、锆石、独居石、磷灰石、云母分离结晶作用后的残余熔体;（3）关键元素的富集和矿化与花岗岩高度分离结晶作用密切相关。随着分异程度的增强,岩浆变为富挥发分的高SiO₂体系,关键金属元素在残余熔体中富集,并且最后可能形成具有工业价值的矿床。由于地球化学特征的相似性,Cs和Tl呈类质同象替代钾、铷进入云母中。富集关键金属元素的花岗岩在时间上和空间上属于与藏南拆离系相关的同构造侵位花岗岩,藏南拆离系的活动促使了原始岩浆的广泛分离结晶作用,以及后期的关键金属元素（如Rb、Cs和Tl）的富集。     

SECOND REPORT (1993) ON THE FIRST THREE GIT-IWG ROCK REFERENCE SAMPLES: ANORTHOSITE FROM GREENLAND, AN-G; BASALTE D'ESSEY-LA-CÔTE, BE-N; GRANITE DE BEAUVOIR, MA-N

The first report (1980) on the three samples, Anorthosite AN-G, Basalt BE-N and Granite MA-N resulted in the chemical characterization of major, minor and 30 trace elements. The present report confirms the validity of a great majority of these working values, in addition to presenting working values for 20 more trace elements for each sample. Only compiled data on trace elements are presented, followed by Tables of statistical parameters used as a basis for their evaluation, both statistical and subjective. A plea is made to obtain more data on platinum group elements and on other "difficult" trace elements (Au, B, Bi, Se, Te, TI, …). The three samples have been processed in 900 kg amounts and, therefore, they are likely to remain available for some decades to come. As such, it is certainly worthwhile to take pains to characterize them well for even these difficult trace elements.     

A stress and displacement discontinuity element method for elastic transversely anisotropic rock

The paper presents closed‐form solutions for stress and displacement influence functions for stress discontinuity (SD) and displacement discontinuity (DD) elements, for a two‐dimensional plane‐strain elastic, transversely anisotropic medium. The solutions for SD elements are based on Kelvin's problem and for DD elements on the concept of dipoles. Stress and displacement influence functions are derived for the following elements: constant SD, linear SD, constant DD, linear DD, square root DD, parabolic DD, constant DD surface, and linear DD surface elements. The formulations are incorporated into FROCK, a hybridized boundary element method code, and are validated by providing comparisons between the results from FROCK and the finite element code ABAQUS. A limited parametric analysis shows the effects of slight anisotropy on the stress field around the tip of a crack and of the orientation of the crack with respect to the axes of elastic symmetry. Copyright © 2014 John Wiley & Sons, Ltd.     

Two New Polish Geological-Environmental Reference Materials: Apatite Concentrate (CTA-AC-1) and Fine Fly Ash (CTA-FFA-1)

World-wide intercomparison runs has made possible the certification of two new Polish geological-environmental reference materials for multi-element trace analysis: Apatite Concentrate (CTA-AC-1) and Fine Fly Ash (CTA-FFA-1). "Recommended values' are established for 25 (CTA-AC-1) and 40 (CTA-FFA-1) elements respectively. In addition, "information values' are assigned for 12 elements in CTA-AC-1 and 10 elements in CTA-FFA-1. Our method of data evaluation has been further improved and a modified version of criteria for assigning recommended and information values is proposed.     

MAJOR, MINOR AND RARE-EARTH ELEMENT DETERMINATIONS IN 25 ROCK STANDARDS BY ICP-ATOMIC EMISSION SPECTROMETRY

Analytical data for 31 elements in 8 Japanese, 12 South African and 5 Belgian Reference Materials of igneous and (meta-) sedimentary origin are reported. These data have been obtained by Inductively Coupled Plasma-Atomic Emission Spectrometry (ICP-AES). For most samples, relative standard deviations are in the range 0.5–3% for major elements, 2–10% for minor elements, and equal to or better than 5% for the REE. Accuracies, as estimated from a comparison with recommended values, are about 10% or better.     

Coupled boundary element/finite element analysis in geomechanics including body forces

A coupling scheme for boundary and finite elements using joint elements is proposed which includes the consideration of body forces. In this scheme the boundary and joint elements are formulated in a similar way as finite elements (i.e., the equivalent FE procedure). These joint elements are efficiently used to combine different BE regions. For the evaluation of a body forces, two methods are compared on computational efficiency and it is found that the method using Galerkin tensor is more efficient than the method dividing the problem domain into several internal cells. Two main geotechnical problems considering self weight are numerically examined using this coupling procedure.     

Analytical perspective on trace element species of interest in exploration

Analysis of soil and sediment samples, using selective extraction methods to distinguish different phases, is of particular interest in exploration geochemistry to locate deeply buried mineral deposits. There are various mechanisms of binding labile elements in the secondary environment, including physical and chemical sorption, precipitation, chelation and complexation. Phases present in soils and sediments which are likely to scavenge ‘free' elements include amorphous Mn and Fe oxides, the humic and fulvic components of humus, and clays. This paper reviews these forms of trace elements and the methods in current use to quantify them. Examples of precision data, both for control and survey samples, are given with respect to trace elements dissolved from the ‘soluble organic' component of humus, Mn oxides and amorphous Fe oxides. The high sensitivity of inductively coupled plasma mass spectrometry (ICP–MS) is required to measure accurately and precisely a large suite of trace elements, especially where only small fractions of elements are dissolved by such leaches as the commercially available Enzyme and MMI (Mobile Metal Ion) extractions. The relative standard deviations (RSD) obtained for 33 elements (e.g. Ag, Cd, In, I) in the standard reference sample (SRM), TILL-2, are in the range 0.5–8% for the hydroxylamine hydrochloride (NH₂OH·HCl) leach designed to extract hydrous Fe and Mn oxides. The corresponding RSDs for elements in the reactive Mn oxide phase extracted by the Enzyme leach are in the range 3–19% except for some trace elements at levels close to detection limit (e.g. Cd, Bi). The RSDs obtained for field duplicates are inferior to those for analytical replicates (i.e. sample splits), probably a reflection of different concentrations of the host phase. In one soil survey, the Fe extracted by a 0.25 M NH₂OH·HCl leach ranged conservatively from 0.2 to 1.7% whereas the Mn extracted by the Enzyme leach varied extensively, from 0.3 to >999 ppm. In contrast, precision, at 1–7% RSD, for field duplicates was found to be comparable with that for both analytical duplicates and the SRM, LKSD-4, for elements associated with the humic and fulvic component of humus samples sieved to <177 μm.     

山东梭罗树地幔橄榄岩微量元素的质子探针研究

作者利用质子微探针和微束ＰＩＸＥ定量分析技术，对山东梭罗树地幔橄榄岩中橄榄石、斜方辉石、单斜辉石、尖晶石和石榴石等矿物的微量元素组成与分布进行了研究。结果表明，不相容元素（Ｓｒ，Ｙ，Ｚｒ）主要富集于单斜辉石内，尖晶石则几乎富集质子探针所能检出的所有微量元素，而石榴石中微量元素含量最少。研究表明，微区微量元素分布很不均匀，推测可能受地幔交代过程中溶液的渗滤效应以及存在微粒包裹体的共同制约。     

锗矿石和铟矿石化学成分分析标准物质研制

目前国内外没有以稀散元素锗、铟为特征元素的矿石标准物质,为了满足我国地质找矿的需求,本文采集广东省韶关凡口铅锌矿作为锗矿石候选物,广西南丹铜坑铅锌矿作为铟矿石候选物,依据国家一级标准物质技术规范,由10家实验室采用化学分析方法和现代仪器分析方法协作定值,研制了1种锗矿石标准物质(GBW07831)和1种铟矿石标准物质(GBW07833)。锗矿石标准物质定值组分为45项,铟矿石标准物质定值组分为47项,包括特征元素、共存元素、稀土元素(15项)、造岩元素和痕量元素,其中锗矿石中锗含量为21.6×10-6,铟矿石中铟含量为39.7×10-6。研制的2种标准物质丰富了我国矿石标准物质的种类,可用于锗、铟矿石化学成分分析测试的量值标准和日常质量监控。