Chemical Characterisation of Geological Raw Materials Used in Traditional Ceramics

A wide range of natural raw materials is used in the manufacture of traditional ceramic products such as ceramic tiles, frits, glazes and pigments. The chemical composition of these raw materials needs to be strictly controlled to assure end-product quality and enable the identification of the origin of defects caused by impurities or contamination. Six types of ceramic raw materials (silica sand, clays and kaolin, feldspars and related minerals, calcium and magnesium carbonates, sodium and calcium borates, and zirconium silicates) have been analysed in this study. X-ray fluorescence (XRF), potentiometry, coulometry and atomic absorption spectrometry (AAS) were used in this chemical characterisation. A methodology has been established for characterising each studied raw material, by identifying the chemical elements to be determined, selecting the most appropriate technique and validating each measurement. The reference materials used for validation were BCS CRM 267, 313/1, 393 and 388 (BAS), GBW 03103, GBW 07404, NIST SRM 181, 201a and 1835, Euronorm CRM 782-1 and Syenite SY-2. The results showed that most of the elements present in the geological samples used as traditional ceramic raw materials could be determined by XRF. The determination of light elements, such as lithium, fluorine and boron, is more suitably conducted by ICP-AES/AAS, potentiometry or potentiometry/ICP-AES respectively. Organic and inorganic carbon could be determined by coulometry. Inorganic carbon (CO₂) could also be determined by coulometry or by thermogravimetry, if samples did not contain clay minerals. Loss on ignition was always determined by gravimetry.     

Petrographic and trace element analysis of uranium-rich tufa calcite, middle Miocene Barstow Formation, California, USA

An integrated petrographic and spectroscopic (X‐ray diffraction, phosphor imaging and synchrotron X‐ray absorption spectroscopy) study of tufas from the Miocene Barstow Formation, California, relates sample morphology, mineralogy and geochemical composition. The tufas, composed mainly of calcite that formed at the interface between an ancient alkaline lake and ground or spring waters, have textures similar to those of microbially mediated terrestrial stromatolites and travertines. The tufas have elevated concentrations of a number of trace elements including Mn, Fe, Sr and U. Synchrotron X‐ray fluorescence analyses show that U concentrations can exceed 500 p.p.m. X‐ray absorption spectroscopy indicates that the U in these samples is incorporated as U(IV). It is suggested here that alkaline lake waters had a high U/Ca ratio and tufa calcite formed where groundwater or (possibly epithermal) springs brought in Ca and trace elements such as Sr. The rapid, and possibly microbially mediated, precipitation of calcite allowed for incorporation of high concentrations of trace metals as either structural substitutes or extremely fine‐scale inclusions.     

Compositional data analysis of Holocene sediments from the West Bengal Sundarbans,India: Geochemical proxies for grain-size variability in a delta environment

This paper is part of a special issue of Applied Geochemistry focusing on reliable applications of compositional multivariate statistical methods. This study outlines the application of compositional data analysis (CoDa) to calibration of geochemical data and multivariate statistical modelling of geochemistry and grain-size data from a set of Holocene sedimentary cores from the Ganges-Brahmaputra (G-B) delta. Over the last two decades, understanding near-continuous records of sedimentary sequences has required the use of core-scanning X-ray fluorescence (XRF) spectrometry, for both terrestrial and marine sedimentary sequences. Initial XRF data are generally unusable in ‘raw-format’, requiring data processing in order to remove instrument bias, as well as informed sequence interpretation. The applicability of these conventional calibration equations to core-scanning XRF data are further limited by the constraints posed by unknown measurement geometry and specimen homogeneity, as well as matrix effects. Log-ratio based calibration schemes have been developed and applied to clastic sedimentary sequences focusing mainly on energy dispersive-XRF (ED-XRF) core-scanning. This study has applied high resolution core-scanning XRF to Holocene sedimentary sequences from the tidal-dominated Indian Sundarbans, (Ganges-Brahmaputra delta plain). The Log-Ratio Calibration Equation (LRCE) was applied to a sub-set of core-scan and conventional ED-XRF data to quantify elemental composition. This provides a robust calibration scheme using reduced major axis regression of log-ratio transformed geochemical data. Through partial least squares (PLS) modelling of geochemical and grain-size data, it is possible to derive robust proxy information for the Sundarbans depositional environment. The application of these techniques to Holocene sedimentary data offers an improved methodological framework for unravelling Holocene sedimentation patterns.     

Assessment of heavy metal contamination in soils around Manali industrial area, Chennai, Southern India

The concentrations of heavy metals (As, Ba, Co, Cr, Cu, Ni, Mo, Pb, Sr, V and Zn) were studied in soils to understand metal contamination due to industrialization and urbanization around Manali industrial area in Chennai, Southern India. This area is affected by the industrial activity and saturated by industries like petrochemicals, refineries, and fertilizers generating hazardous wastes. The contamination of the soils was assessed on the basis of geoaccumulation index, enrichment factor (EF), contamination factor and degree of contamination. Soil samples were collected from the industrial area of Manali from the top 10-cm-layer of the soil. Soil samples were analyzed for heavy metals by using Philips MagiX PRO-2440 Wavelength dispersive X-ray fluorescence spectrometry. The data revealed elevated concentrations of Chromium (149.8–418.0 mg/kg), Copper (22.4–372.0 mg/kg), Nickel (11.8–78.8 mg/kg), Zinc (63.5–213.6 mg/kg) and Molybdenum (2.3–15.3 mg/kg). The concentrations of other elements were similar to the levels in the earth’s crust or pointed to metal depletion in the soil (EF < 1). The high-EFs for some heavy metals obtained in the soil samples show that there is a considerable heavy metal pollution, which could be correlated with the industries in the area. Contamination sites pose significant environmental hazards for terrestrial and aquatic ecosystems. They are important sources of pollution and may result in ecotoxicological effects on terrestrial, groundwater and aquatic ecosystems. In this perspective there is need for a safe dumping of waste disposal in order to minimize environmental pollution.     

GGR Critical Review of Analytical Developments in 2006–2007

In 2005 the Geostandards and Geoanalytical Research editorial team, in the true spirit of scientific endeavour, embarked on an experiment of our own. We decided to trial a new kind of review, somewhat different from those more typically observed in journals, and one that would provide readers with a summary of analytical developments across a broad range of topics appropriate to the Earth sciences. The first contribution of this kind appeared in 2005, and reported on developments in 2003 (Hergt et al. 2005). The second, this time a biennial review, was published in 2006 and reported on highlights of the 2004 and 2005 literature (Hergt et al. 2006). Based on reprint requests, positive remarks at conferences and strong citations we consider the experiment a resounding success and proudly present here the third in this series. This comprises six individual review sections that cover the main analytical technologies and topical application fields in geoanalysis and geochemistry, including geological and environmental reference materials, ICP‐thermal and secondary ionisation‐mass spectrometry, as well as neutron activation analysis, X‐ray fluorescence and atomic absorption spectrometry.     

浙江下王渡遗址中晚全新世古环境演变及人类活动初步研究

通过对浙江宁奉平原下王渡遗址剖面样品的孢粉以及地化元素分析,结合5个AMS14C年代数据及考古学文化分层,揭示了河姆渡晚期文化时期及良渚时期该遗址所在区域环境变化及人类活动响应。研究表明：该遗址区温暖湿润的气候条件为河姆渡先民的定居创造了条件,植被面貌以常绿落叶阔叶混交林为主。孢粉及地化元素等证据表明中全新世的海侵使得该遗址区发生了一次文化中断,海洋的影响从河姆渡文化第四期开始逐渐消退。从这一时期开始,草本植物花粉占比很大程度地超过乔灌木植物花粉,特别是粒径不小于37 μm禾本科花粉含量的增加,推测为栽培作物类型。花粉信号揭示了人类活动对自然环境的改造开始逐渐加强,在下王渡遗址区附近可能出现有一定规模的水稻种植区。     

X射线荧光法在茅排金矿床的应用

简述Ｘ射线荧光法（ＸＲＦ）的工作原理和工作方法,介绍了该方法在茅排金矿野外工作情况,详细讨论了不同源发源、不同滤片对及组合滤片对对相同剖面和不同剖面的测量结果,分析了野外和室内出现差异的原因,最后提出了看法。     

Characterization of Banded Iron Formations by Two-Dimensional XRF Imaging and XANES Analyses

Abstract: Synchrotron radiation-induced X–ray fluorescence (SR–XRF) and conventional X-ray fluorescence (XRF) analyses were applied to determine the distributions of iron, manganese, calcium, titanium, and silicon, and chemical forms of iron and trace manganese in three banded iron formation (BIF) samples. The XRF imagings on the weathered and altered BIF from the Cleaverville Formation (3. 3–3. 1 Gyr), Western Australia, showed redistributions of iron, calcium, and manganese with the disappearance of the primary bandings, while, in contrast, titanium preserved its primary depositional distribution. The XRF imagings on the BIF from the Hamersley Group (2. 5 Gyr), Western Australia, showed that manganese and titanium distribute originally at boundary region between the iron-rich mesoband and the silica-rich mesoband. The X-ray Absorption Near Edge Structure (XANES) analysis revealed that the chemical forms of manganese and iron well represent the rhythmic change of the bandings.     

基于XRF的紫金山铜矿床硫地质特征

福建紫金山铜矿床属高硫浅成中低温热液矿床,矿石中主要含铜矿物为蓝辉铜矿、铜蓝和硫砷铜矿等,且铜矿物与黄铁矿密切共生。由于铜矿石中硫含量较高,导致铜精矿中硫含量超标,w(S)/w(Cu)比值为2.0~2.1,远高于冶炼要求的1.15~1.20,影响其经济价值。使用X射线荧光(XRF)光谱分析对紫金山铜矿中S元素的分布进行数字化研究,查明硫的空间分布规律和赋存状态,划分铜矿石类型,为紫金山铜矿今后的采选工作提供参考。