Development and calibration of a WDXRF routine applied to provenance studies on archaeological ceramics

Elemental analysis of ancient ceramics is primarily used in provenance research, where defined compositional groups are attributed to particular raw materials sources or production locations. Requirements in data quality and analytical performance are high, as is the need for clear and reproducible methodologies and the availability of information on the above to ensure interlaboratory comparability and long‐term data validity. This paper outlines the measurement parameters of a dedicated calibration set‐up for the analysis of ancient ceramics using wavelength‐dispersive X‐ray fluorescence spectrometry. The specimens are prepared as concentrated glass beads, allowing the measurement of 26 elements from a single sample, thus minimising sample size requirements. Certified and non‐commercial standards are used to evaluate the performance of the method in terms of detection limits, precision, repeatability and accuracy. The materials used cover a range of compositions in line with the matrix variability encountered in archaeological ceramics. The data confirm the high standard of the method and highlight specific limitations. An initial assessment of comparability with other set‐ups used in ceramic analyses, primarily neutron activation analysis, is given through a discussion of performance on commonly analysed materials. The advantages of the proposed method include excellent analytical performance, analysis of a large suite of elements including all major, minor and a good range of traces, relatively small sample sizes and preparation of samples that can be stored and reanalysed. Copyright © 2017 John Wiley & Sons, Ltd.     

Thickness determination of gold layer on pre‐Columbian objects and a gilding frame,combining pXRF and PLS regression

In conservation, restoration and characterization studies of art and archaeological objects, the improvement of analytical techniques is a tendency. X‐ray fluorescence (XRF) is a versatile technique, and it has been widely used in the last decades for characterization of a great variety of materials (metals, glass, paints, inks, ceramics, etc.) applied to cultural heritage studies. Besides the chemical composition, it is possible to infer the layer thickness through XRF, enabling a general knowledge of the manufacturing techniques implemented by the culture of origin, as well as the association with the technological level reached for the production of each kind of artefact. The aim of this study is to introduce an alternative way for gold thickness determination of coatings in cultural heritage objects, combining portable XRF data and partial least square regression. As a case of study, we present the use of this methodology in portable XRF measurements performed in situ on a gilding frame in Brazil and in two pre‐Columbian artefacts from Chavin culture in Peru. Gold layers with thicknesses determined by Rutherford backscattering spectrometry (RBS) were used as standards to perform a calibration model and to check the methodology before its application to unknown artefacts. Copyright © 2016 John Wiley & Sons, Ltd.     

南海一号出水景德镇窑与龙泉窑青瓷特征的无损分析研究

古代陶瓷产地研究是陶瓷考古的重要内容,也是科技考古工作者研究的重点。目前国内古代陶瓷产地研究主要依赖化学成分分析技术,对陶瓷釉层结构特征的无损分析研究却相对缺乏,难以对古代陶瓷进行全方位的认知。该研究首次将光学相干层析(OCT)与X射线荧光(XRF)光谱分析技术相结合,对南海一号沉船出水的南宋初期景德镇窑和龙泉窑青瓷瓷釉的断层结构特征和化学成分特征进行综合无损分析研究。首先采用扫频OCT成像系统对两个窑址青瓷瓷釉断层结构及装饰工艺特征进行了研究,分析了青瓷瓷釉类型、釉层厚度、釉层内气泡、包裹体、表面裂纹等特征及分布状况,对比了两窑址青瓷瓷釉断层结构特征,确定了可能采用的装饰工艺。其次,利用X射线荧光(XRF)光谱分析获得了两窑址青瓷胎釉的化学成分,对比研究了两个窑址青瓷胎釉化学成分差异,进而探讨了瓷釉断层OCT图像特征与釉层化学成分之间存在的联系。实验结果表明,景德镇青瓷和龙泉青瓷样品在釉层厚度、气泡、裂纹、包裹体等瓷釉断层结构特征上差异明显,在胎釉化学成分方面,两类青瓷在胎釉着色相关元素、釉层碱性氧化物等成分含量上也存在差异。同时,瓷釉断面结构特征差异与釉层化学成分差异存在紧密联系。实验证明,将OCT与XRF相结合是一种有效的辨别瓷器窑口的科学技术方法。     

Identification of mineral inclusions in archaeological ceramics using microbeam X‐ray fluorescence spectrometry

Archaeological ceramics are subjected to chemical and geochemical analyses in order to ascertain production techniques and provenance. Many analytical techniques are currently available for the determination of qualitative and quantitative characteristics pertaining to clay composition and structure. Microbeam XRF is utilised in this report to analyse mineral inclusions present in Mleiha ceramics in order to establish better provenance data. A total of 67 mineral inclusions of different sizes and colours were analysed. The majority of the sampled inclusions (94%) were silicates, and only 6% were calcites. A total of 35 inclusions from the former group were olivine minerals composed of a mixture of Mg, Si, and Fe oxides constituting 87–99% of the inclusions' mass, in addition to 13 inclusions composed mainly of Al, Si, and Ca oxides with sum concentrations ranging from 80% to 98%. Copyright © 2014 John Wiley & Sons, Ltd.     

Approaches to solid sample preparation based on analytical depth for reliable X‐ray fluorescence analysis

In this paper, we discuss approaches to prepare solid samples for X‐ray fluorescence spectrometry (XRF). Although XRF can be used to analyze major and minor elements in various solid samples including powders and grains without dissolution techniques, to obtain reliable XRF results, the prepared sample must meet certain criteria related to homogeneity, particle size, flatness, and thickness. The conditions are defined by the analytical depth of fluorescent X‐rays from analytes, and the analytical depth can be estimated from the X‐ray absorption related to the energy of each X‐ray and the composition and density of the sample. For example, when the sample flatness and particle size are less than the analytical depth and the sample possesses homogeneity within a depth less than the analytical depth, the XRF results are representative of the entire sample. Furthermore, an appropriate sample thickness that is larger than the analytical depth or constant can prevent changes in fluorescent X‐ray intensity with variations in sample thickness. To obtain accurate and reproducible measurements, inhomogeneous solid samples must be pulverized, homogenized, and prepared as loose powder, powder pellets, or glass beads. This paper explains the approaches used to prepare solid samples for XRF analysis based on the analytical depths of fluorescent X‐rays. Copyright © 2016 John Wiley & Sons, Ltd.     

A sample carrier for measuring discrete powdered samples with an ITRAX XRF core scanner

The elemental composition of discrete powdered sediment samples can be measured by the energy‐dispersive X‐ray fluorescence (XRF) system that is installed in XRF core scanners. Because an appropriate sample carrier for powdered samples is currently not available, for example, for the ITRAX XRF core scanner, such a carrier is presented in this technical note. The designed sample carrier can hold 30 sample cups with a volume of 0.88 cm³ each. A maximum of 5 sample carriers, that is, 150 samples, can be measured in one run. The sample cups and carriers are optimized for a measurement procedure with a step size of 5 mm and variable count times up to 100 s per sample. With this setting, data are collected from an area of 100 mm² in the center of the sample thereby ensuring a good representativeness of the signal because potential sample inhomogeneity is accounted for. Because the described sample carrier system allows rapid element analyses of discrete powdered environmental samples with an XRF core scanner, it may in some cases represent a time‐ and cost‐efficient alternative to conventional XRF analyses.     

Analytical Study of Raw Materials of Zinc Oxide Used for Enamels on Industrial Ceramics: Quantitative Analysis of Zinc,Lead, and Sulfur in These Samples by X‐ray Fluorescence and Flame Atomic Absorption Spectrometry

An analytical study is carried out to optimize X‐ray fluorescence (XRF) and flame atomic absorption spectrometry (FAAS) quantitative analysis of Zn, Pb, and S in ZnO samples commonly used to obtain industrial ceramic enamels. Pb and S in the raw materials often contaminate ZnO and are very detrimental in industrial applications. Thus, very accurate analytical determination of these elements in ceramic samples is extremely important. First of all, a mineralogical study by X‐ray diffraction (XRD) on the different components in these raw materials and the materials produced during the firing process is performed in order to establish the mineral forms in a reference sample for analysis by XRF spectrometry. The working conditions are optimized for XRF multielemental analysis, using the sample in the form of pellets, due to high loss on ignition (LOI) values. The preparation of suitable standards and working conditions for FAAS analysis have also been optimized. The content of these elements was determined by FAAS for the reference sample and several samples for industrial use, and the results were compared with those obtained by XRF. Comparison of the results obtained from XRF and FAAS analysis of Pb and Zn show more accurate values for FAAS. For ZnO, an accuracy of 0.11% with ±0.1% precision by FAAS and 0.46% accuracy with ±0.2% precision by XRF are found. For PbO, 1.06% accuracy and ±0.06% precision using FAAS and 5.6% accuracy and ±0.35% precision by XRF were found. For SO₃ determined only by XRF, accuracy was 4.76% with ±0.25% precision. These values are highly satisfactory given that these two elements are only found in small proportions.     

Direct chemical characterisation of clay suspensions by WD‐XRF

This study was performed to develop a method for directly controlling the chemical composition of clay slurries used in preparing ceramic floor and wall tile bodies by wavelength‐dispersive X‐ray fluorescence (WD‐XRF) spectrometry, without the prior need to dry and prepare the samples as fused beads or pellets for WD‐XRF measurement, owing to the importance of knowing the suspension chemical composition in real time for appropriate control of the industrial process. The study was conducted on a wide range of ceramic floor and wall tile bodies, which are used to prepare different suspensions. The influence of suspension viscosity (from 300 to 7000 cp), of suspension solids content (between 66 and 69%), and of the type of body composition (floor or wall tile) on the WD‐XRF measurement was determined. In these viscosity and solid content ranges, no appreciable differences were observed in the WD‐XRF measurement results, indicating that the possibly arising variations in viscosity and solids content in such clay suspensions in industrial practice do not influence the WD‐XRF measurement. In contrast, the type of body composition did influence the WD‐XRF measurement. The developed method is rapid, reproducible, and accurate, which was verified by analysis of the materials using the customary method of WD‐XRF measurement on fused beads. In addition, this method is cheaper and more harmless to the environment; it minimises waste generation, since no sample preparation is required and the plastic sample holders can be reused, thanks to the reusable sample holder system designed at the Instituto de Tecnología Cerámica laboratories. Copyright © 2011 John Wiley & Sons, Ltd.     

Extraterrestrial Mössbauer spectrometry

We describe a combined backscatter Mössbauer spectrometer and X-ray fluorescence analyzer (BaMS/XRF) instrument suitable for planetary missions to the surfaces of Mars (MESUR Program), the Moon, asteroids, or other solid solar-system objects. The BaMS/XRF instrument is designed to be capable of concurrent analysis of a sample for its elemental abundances (XRF) and for the mineralogy of its iron-bearing phases (BaMS) without any sample preparation.     

Confocal macro X‐ray fluorescence spectrometer on commercial 3D printer

Novel confocal X‐ray fluorescence (XRF) spectrometer was designed and constructed for 3D analysis of elementary composition in the surface layer of spatially extended objects having unlimited chemical composition and geometrical shape. The main elements of the XRF device were mounted on a moving frame of a commercial 3D printer. The XRF unit consists of a silicon drift detector and a low‐power transmission‐type X‐ray tube. Both the excitation and secondary X‐ray beams were formed and regulated by simple collimator systems in order to create a macro confocal measuring setup. The spatial accuracy of the mechanical stages of the 3D printer achieved was less than 5 μm at 100‐μm step‐size. The diameter of the focal spot of the confocal measuring arrangement was between 1.5 and 2.0 mm. The alignment of the excitation and secondary X‐ray beams and the selection of the measuring spot on the sample surface were ensured by two laser beams and a digital microscope for visualization of the irradiated spot. The elements of the optical system together with the XRF spectrometer were mounted on the horizontal arm of the 3D printer, which mechanical design is capable of synchronized moving the full spectroscopic device within vertical directions. Analytical capability and the 3D spatial resolution of the confocal spectrometer were determined. Copyright © 2017 John Wiley & Sons, Ltd.     

ED‐XRF set‐up for size‐segregated aerosol samples analysis

The knowledge of size‐segregated elemental concentrations in atmospheric particulate matter (PM) gives a useful contribution to the complete chemical characterisation; this information can be obtained by sampling with multi‐stage cascade impactors. In this work, samples were collected using a low‐pressure 12‐stage Small Deposit Impactor and a 13‐stage rotating Micro Orifice Uniform Deposit Impactor^?. Both impactors collect the aerosol in an inhomogeneous geometry, which needs a special set‐up for X‐ray analysis. This work aims at setting up an energy dispersive X‐ray fluorescence (ED‐XRF) spectrometer to analyse quantitatively size‐segregated samples obtained by these impactors. The analysis of cascade impactor samples by ED‐XRF is not customary; therefore, as additional consistency test some samples were analysed also by particle‐induced X‐ray emission (PIXE), which is more frequently applied to size‐segregated samples characterised by small PM quantities. A very good agreement between ED‐XRF and PIXE results was obtained for all the detected elements in samples collected with both impactors. The good inter‐comparability proves that our methodology is reliable for analysing size‐segregated samples by ED‐XRF technique. The advantage of this approach is that ED‐XRF is cheaper, easier to use, and more widespread than PIXE, thus promoting an intensive use of multi‐stage impactors. Copyright © 2011 John Wiley & Sons, Ltd.     

Microfluidic sample preparation for elemental analysis in liquid samples using micro X‐ray fluorescence spectrometry

The integration of microfluidic devices with micro X‐ray fluorescence (micro‐XRF) spectrometry offers a new approach for the direct characterization of liquid materials. A sample presentation method based on use of small volumes (<5 µl) of liquid contained in an XRF‐compatible device has been developed. In this feasibility study, a prototype chip was constructed, and its suitability for XRF analysis of liquids was evaluated, along with that of a commercially produced microfluidic device. Each of the chips had an analytical chamber which contained approximately 1 µl of sample when the device was filled using a pipette. The performance of the chips was assessed using micro‐XRF and high resolution monochromatic wavelength dispersive X‐ray fluorescence, a method that provides highly selective and sensitive detection of actinides. The intended application of the device developed in this study is for measurement of Pu in spent nuclear fuel. Aqueous solutions and a synthetic spent fuel matrix were used to evaluate the devices. Sr, which has its Kα line energy close to the Pu Lα line at 14.2 keV, was utilized as a surrogate for Pu because of reduced handling risks. Between and within chip repeatability were studied, along with linearity of response and accuracy. The limit of detection for Sr determination in the chip is estimated at 5 ng/µl (ppm). This work demonstrates the applicability of microfluidic sample preparation to liquid characterization by XRF, and provides a basis for further development of this approach for elemental analysis within a range of sample types. Copyright © 2014 John Wiley & Sons, Ltd.     

A multi‐technique approach for the characterization of decorative stones and non‐destructive method for the discrimination of similar rocks

In this paper, a multi‐technique approach, at different scale of observation, is used to characterize a group of decorative stones and to permit to distinguish rocks with similar aspect but coming from different areas. In particular, the samples under study are sedimentary and metamorphic rocks, widely used as building blocks of modern and historical constructions and sculptures. The petrographic and mineralogical features of such rocks were performed by optical microscopy and Raman and Fourier transform infrared absorbance spectroscopies. These techniques permitted to obtain a complete structural, textural, and mineralogical characterization. At elemental level, the investigation was carried out by X‐ray fluorescence (XRF). In particular, XRF and Raman measurements were collected using portable instrumentations, whose advantages for the in situ analysis have been pointed out. The obtained results evidenced the high discriminant capability of the portable XRF for the decorative stones especially when this method is coupled with mineralogical and petrographic information. In this context, we propose to create a database for precious ornamental stones, which could be a starting point for a non‐destructive characterization, even useful for provenance study and/or certification of origin. Copyright © 2013 John Wiley & Sons, Ltd.     

Development of a compact XRF probe using a ring‐type secondary target

Recently, on‐site analysis is being performed in many fields, and the use of compact instruments is required. In this article, we developed a compact x‐ray fluorescence (XRF) probe using a ring‐type secondary target. Employing the ring‐type target, coaxial optical geometry (irradiation and detection) could be achieved. We applied this probe to standard steel materials and standard solutions. In addition, a solid sample in solution was directly measured. As an application of the XRF probe, the monitoring of a chemical reaction was demonstrated that enabled observation of an increase in metallic ions. Copyright © 2008 John Wiley & Sons, Ltd.     

Multi‐technique study of archaeological cord‐marked wares decorated with red coatings from Taiwan

Archaeological finds of Neolithic to Iron Age pottery show clay potsherds characterized by red cord‐markings. The items date back from 5500 to 1500 B.P. To better understand temporal changes in the provenance of raw‐material sources, and the nature of materials used in the red colorant and ceramic bodies, micro‐Raman spectroscopy, X‐ray diffraction analysis (XRD), and micro X‐ray florescence spectroscopy (μXRF) were applied to 29 red‐coated potsherd samples found at twelve archaeological sites across Taiwan. The techniques identified the chemical and mineralogical composition of the red coatings and ceramic bodies as well as the production methods of ancient potters. Eighteen mineral phases were identified from the Raman spectra, including hematite, α‐quartz, and anatase. Feldspar, rutile, pyroxenes, calcite, gypsum, amorphous carbon, and graphite were also detected. XRD measurements, and μXRF analyses were used as complementary techniques to obtain mineral and chemical compositions. Hematite, anatase, calcite, plagioclase feldspar, and illite were present in potsherds, suggesting pottery produced from illitic clays fired at less than 850 °C under oxidizing conditions. Results further suggest that raw materials were sourced from or near local volcanic rock areas, and more broadly from metamorphic or sedimentary rocks and clays. Chemically, raw materials used for red coatings are different to those of the ceramic bodies. Objects from most sites used the same raw material sources; however, some sites contain objects made from changing sources over time. Pot coatings exhibit polygonal cracks, and loosened cementation strongly suggesting that finely processed moist clays were fired to a biscuit form with no second stage firing process. The non‐destructive Raman experiments identified and characterized mineral phases, which helped understand manufacturing techniques. Overall the multi‐technique approach gave extensive information on the finds, helping to differentiate raw material sources and production technologies. This approach is an important and effective method for investigating archaeological finds. Copyright © 2014 John Wiley & Sons, Ltd.     

Depth‐selective elemental imaging of microSD card by confocal micro XRF analysis

A semiconductor device, a microSD card, was measured by using two XRF instruments. 2D elemental images were obtained using a micro‐XRF system with a spatial resolution of 10 µm. Elemental distributions of the near‐surface region of the sample were clearly shown. Titanium was observed in the resin constituting the sample. Nickel and gold were observed on a terminal and localization of the sample. Elemental distribution of copper reflected the circuit structure of the measurement area that was in the neighborhood of the sample surface. Moreover, the elemental depth distributions of the sample were measured by using a confocal micro‐XRF instrument. The confocal micro‐XRF instrument was constructed in the laboratory with fine‐focus polycapillary x‐ray optics. The depth resolution of the developed spectrometer was 13.7 µm at an energy of Au Lβ (11.4 keV). The elemental images obtained at near‐surface by confocal micro‐XRF were the same as the results obtained from 2D micro‐XRF. However, different Cu images were obtained at a depth of several tens of micrometers. This indicates that microSD cards consist of a few different Cu‐circuit structure designs. The elemental depth distributions of each circuit structure of the semiconductor device were clearly shown by confocal micro‐XRF. Copyright © 2013 John Wiley & Sons, Ltd.     

Methodological challenges of optical tweezers‐based X‐ray fluorescence imaging of biological model organisms at synchrotron facilities

Recently, a radically new synchrotron radiation‐based elemental imaging approach for the analysis of biological model organisms and single cells in their natural in vivo state was introduced. The methodology combines optical tweezers (OT) technology for non‐contact laser‐based sample manipulation with synchrotron radiation confocal X‐ray fluorescence (XRF) microimaging for the first time at ESRF‐ID13. The optical manipulation possibilities and limitations of biological model organisms, the OT setup developments for XRF imaging and the confocal XRF‐related challenges are reported. In general, the applicability of the OT‐based setup is extended with the aim of introducing the OT XRF methodology in all research fields where highly sensitive in vivo multi‐elemental analysis is of relevance at the (sub)micrometre spatial resolution level.     

A simple calibration procedure of polycapillary based portable micro‐XRF spectrometers for reliable quantitative analysis of cultural heritage materials

Portable micro‐X‐ray fluorescence (micro‐XRF) spectrometers mostly utilize a polycapillary X‐ray lens along the excitation channel to collect, propagate and focus down to few tens of micrometers the X‐ray tube radiation. However, the polycapillary X‐ray lens increases the complexity of the quantification of micro‐XRF data because its transmission efficiency is strongly dependent on the lens specifications and the propagated X‐ray energy. This feature results to a significant and not easily predicted modification of the energy distribution of the primary X‐ray tube spectrum. In the present work, we propose a simple calibration procedure of the X‐ray lens transmission efficiency based on the fundamental parameters approach in XRF analysis. This analytical methodology is best suited for compact commercial and portable micro‐XRF spectrometers. The developed calibration procedure is validated through the quantitative analysis of a broad range of samples with archeological relevance such as glasses, historical copper alloys, silver and gold alloys offering an overall accuracy of less than 10%–15%. Copyright © 2015 John Wiley & Sons, Ltd.     

Application of high‐energy polarized energy‐dispersive x‐ray fluorescence spectrometry to the determination of trace levels of As,Hg, and Pb in certifiable color additives

Advances in x‐ray fluorescence (XRF) using high‐energy polarized energy‐dispersive (ED)XRF spectrometry (PEDXRF) were applied to the determination of trace As, Hg, and Pb in various color additives subject to batch certification by the U.S. Food and Drug Administration (FDA). The objectives of this study were to simplify sample preparation for quantitative determination of these elements and, if possible, to achieve improved sensitivity and detection limits compared to techniques currently used for certification. PEDXRF was compared with wavelength‐dispersive x‐ray fluorescence spectrometry (WDXRF) and inductively coupled plasma – mass spectrometry (ICP‐MS) for the analysis of trace levels of As, Hg, and Pb in certifiable color additives. For these light matrices, PEDXRF provided better signal‐to‐noise and allowed quantitation in smaller amounts of color additive relative to WDXRF and equal or better precision to ICP‐MS. Determination of these trace elements in a variety of color additives was possible relative to calibrations generated from one color additive using specimens prepared simply by pouring the color additive powder into an XRF sample cup. Published 2016. This article is a U.S. Government work and is in the public domain in the USA