A new X-ray pinhole camera for energy dispersive X-ray fluorescence imaging with high-energy and high-spatial resolution

A new X-ray pinhole camera for the Energy Dispersive X-ray Fluorescence (ED-XRF) imaging of materials with high-energy and high-spatial resolution, was designed and developed. It consists of a back-illuminated and deep depleted CCD detector (composed of 1024 × 1024 pixels with a lateral size of 13 μm) coupled to a 70 μm laser-drilled pinhole-collimator, positioned between the sample under analysis and the CCD. The X-ray pinhole camera works in a coaxial geometry allowing a wide range of magnification values.The characteristic X-ray fluorescence is induced on the samples by irradiation with an external X-ray tube working at a maximum power of 100 W (50 kV and 2 mA operating conditions).The spectroscopic capabilities of the X-ray pinhole camera were accurately investigated. Energy response and energy calibration of the CCD detector were determined by irradiating pure target-materials emitting characteristic X-rays in the energy working-domain of the system (between 3 keV and 30 keV).Measurements were performed by using a multi-frame acquisition in single-photon counting. The characteristic X-ray spectra were obtained by an automated processing of the acquired images. The energy resolution measured at the Fe–Kα line is 157 eV.The use of the X-ray pinhole camera for the 2D resolved elemental analysis was investigated by using reference-patterns of different materials and geometries. The possibility of the elemental mapping of samples up to an area of 3 × 3 cm² was demonstrated.Finally, the spatial resolution of the pinhole camera was measured by analyzing the profile function of a sharp-edge. The spatial resolution determined at the magnification values of 3.2 × and 0.8 × (used as testing values) is about 90 μm and 190 μm respectively.     

Wavelength dispersive X-ray fluorescence imaging using a high-sensitivity imaging sensor

A new wavelength-dispersive X-ray fluorescence (WD-XRF) imaging spectrometer equipped with a high-sensitivity imaging sensor was developed in our laboratory. In this instrument, a straight polycapillary optic was applied instead of a Soller slit as well as a 2D imaging X-ray detector instead of X-ray counters, which are used in conventional WD-XRF spectrometers. Therefore, images of elemental distribution were available after a short exposure time. Ni Kα images and Cu Kα images were clearly obtained at corresponding diffraction angles for a short exposure time of 10 s. By optimizing the spectrometer, the time required for imaging is reduced, leading to XRF image movies. It is difficult to distinguish two peaks (Ti Kα (4.508 keV) and Ba Lα (4.465 keV)) due to the poor energy resolution of EDXRS. However, Ti and Ba images could be successfully observed by the WD-XRF imaging spectrometer. The energy resolution of the developed spectrometer was 25 eV at the Ti Kα peak.     

Performance of triple coincidence imaging as an addition to dedicated PET

In this work, we investigate the performance of semiconductor detectors imaging capabilities in three-photon annihilation processes in order to combine this novel imaging modality with conventional positron emission tomography. The spatial resolution is studied as a function of detector positions and selected energy window. This was measured from different experimental arrangements and found to be in the range between 3.3–3.9 cm with a mean of 3.5±0.1 cm. Scatter and random events, coincidence timing resolution and count rate performance are discussed.     

A combined laser-induced breakdown and Raman spectroscopy Echelle system for elemental and molecular microanalysis

Raman and laser-induced breakdown spectroscopy is integrated into a single system for molecular and elemental microanalyses. Both analyses are performed on the same ~ 0.002 mm² sample spot allowing the assessment of sample heterogeneity on a micrometric scale through mapping and scanning. The core of the spectrometer system is a novel high resolution dual arm Echelle spectrograph utilized for both techniques. In contrast to scanning Raman spectroscopy systems, the Echelle–Raman spectrograph provides a high resolution spectrum in a broad spectral range of 200–6000 cm^? 1 without moving the dispersive element. The system displays comparable or better sensitivity and spectral resolution in comparison to a state-of-the-art scanning Raman microscope and allows short analysis times for both Raman and laser induced breakdown spectroscopy. The laser-induced breakdown spectroscopy performance of the system is characterized by ppm detection limits, high spectral resolving power (15,000), and broad spectral range (290–945 nm). The capability of the system is demonstrated with the mapping of heterogeneous mineral samples and layer by layer analysis of pigments revealing the advantages of combining the techniques in a single unified set-up.     

Simultaneous multielement detection in particle beam/hollow cathode-optical emission spectroscopy

Presented here is the development of a particle beam/hollow cathode-optical emission spectroscopy source that has been interfaced with a high resolution polychromator for use as a species-specific detector for chromatographic separations. Use of the high resolution JY RF-5000 polychromator allows simultaneous, multielement analysis; a necessary requirement for comprehensive speciation analysis. Parametric optimization was performed for the nebulization conditions, desolvation temperature, glow discharge current and pressure, and the source block temperature (vaporization) using nitrate salts containing lead, nickel, and silver. Peak area, height, and width were recorded for optical emission of Pb (I) 220.35 nm, Ni (I) 341.41 nm, and Ag (I) 338.28 nm in order to determine optimal peak characteristics under chromatographic separation conditions. Response curves for a multielement salt solution containing Pb, Ni, and Ag were obtained using the optimized conditions, with detection limits for triplicate injections of 2.2, 0.17, and 0.19 ng, respectively. The ability to monitor multiple elements simultaneously reveals the existence of interelement matrix effects that have not been noted previously in hollow cathode devices. The ability to monitor metals and non-metals is demonstrated towards the future application of this system as a tool for metallomic studies.     

Evaluation of the diffusion of Mn,Fe, Ba and Pb in Middle Ages human teeth by synchrotron microprobe X-ray fluorescence

Human teeth from the Middle Ages have been analysed using a synchrotron microprobe evaluating Mn, Fe, Ba and Pb diffusion from the soil into the tooth structure. It is apparent that post-mortem teeth of ancient populations are influenced by the endogenous environment. The diffusion pattern of some elements can give information both for archaeological purposes and diagenesis processes affecting the apatite ante-mortem elemental content.An X-ray fluorescence set-up with microprobe capabilities, 100 μm of spatial resolution and energy of 18 keV, installed at LURE synchrotron (France) was used. Line scans were performed along the several regions of the teeth, in steps of 100 to 1000 μm. Ba is much enriched in ancient teeth when compared to recent ones, where this element is almost non-existent. Furthermore, the concentration profiles show increased levels of this element close to the external enamel region, reaching values up to 200 μg g^− 1 decreasing in dentine and achieving a steady level in the inner dentine and root. Pb concentration profiles show strongly increased levels of this element close to the external enamel region (20 μg g^− 1), decreasing strongly to the inner part of the dentine (0.5 μg g^− 1) contrarily to the normal situation in modern citizens where the highest concentrations for Pb are in the inner root dentine. This behaviour suggests post-mortem uptake from the soil; the presence of elevated levels of Pb can be explained by the fact that this burial place was a car park for more than 20 years.The distribution of Mn and Fe follow very similar patterns and both are very much enriched especially in the outer surfaces in contact with the soil, showing strong contamination from the soil.     

Characterization of an energy dispersive X-ray fluorescence imaging system based on a Micropattern Gaseous Detector

An energy dispersive X-ray fluorescence (EDXRF) imaging system based on a Micropattern Gas Detector has already shown good results for different applications. An X-ray tube, a pinhole camera and a Micro-Hole and Strip Plate (MHSP) based detector are the main components of the experimental system. The detector uses an MHSP in a Xe atmosphere at 1 bar, and acting as a photon counting device, i.e., it is capable to record each single event retaining the energy and the interaction position (2D-sensitive detector) information of the incident photon, demonstrating to be a promising device for EDXRF imaging applications. This work presents studies of energy resolution, energy linearity and spatial resolution/elemental mapping as a function of image magnification of the system.     

Kβ/Kα X-ray intensity ratios for elements in the range 16⩽Z⩽92 excited by 5.9, 59.5 and 123.6 keV photons

The K shell intensity ratios K_β/K_α for 59 elements in the atomic region 16⩽Z⩽92 have been measured at excitation energies of 5.9, 59.5 and 123.6 keV. K X-rays emitted by samples have been counted by a Si(Li) detector with resolution 160 eV at 5.9 keV. The measured values were compared with the theoretical values calculated using Scofield's tables based on the Hartree–Slater and Hartree–Fock theories and available experimental values. Reasonable agreement is typically obtained between present and theoretical values.     

Iron,copper, zinc and bromine mapping in cirrhotic liver slices from patients with hemochromatosis studied by microscopic synchrotron radiation X-ray fluorescence analysis in continuous scanning mode

Iron (Fe) and copper (Cu) are essential metals in physiological cell metabolism. While Fe is easy to determine biochemically in histological slices, Cu and zinc (Zn) distribution is frequently critical in confirming the presence of an overload in disturbed Fe/Cu metabolism. To analyze Fe, Cu and Zn in a near histological resolution, energy dispersive microscopic synchrotron radiation X-ray fluorescence was applied.In normal liver tissue, after fixation and imbedding in paraffin, mean Fe, Cu and Zn concentrations were 152 ± 54, 20.1 ± 4.3 and 88.919.5 μg/g sample weight, respectively. No substantial, characteristic differences in their distribution were found in the two-dimensional scans. In slices from patients with hemochromatosis mean Fe, Cu and Zn concentrations were 1102 ± 539, 35.9 ± 14.6 and 27.2 ± 6.7 μg/g sample weight, respectively. Additionally, a significant decrease in phosphorus and sulphur concentrations existed. An increased Cu around cirrhotic regenerations nodules is mostly associated with a lymphocytic infiltration in this region. Analyzing concentrations of Fe in different regions of the samples show a clear negative dependency between Fe and Cu, Cu and Zn, but a positive one between Fe and Zn.Conclusion: With a focal beam size of 15 μm in diameter a resolution of the elemental distribution was achieved which is widely comparable with stained histological slices (20× light microscope). The analysis of simultaneous determined elements reveals metabolic differences between Fe, Cu and Zn in liver tissue from patients with hemochromatosis.     

Determination of K shell fluorescence cross-section and Kβ/Kα intensity ratios for Fe,Se, Te,FeSe, FeTe and TeSe

The fluorescence cross-sections (σ_Ki) and the intensity ratios K_β/K_α for pure Fe, Se, Te elements and FeSe, FeTe, TeSe complexes have been investigated. The samples were excited by 59.5 keV γ-rays from ²⁴¹Am annular radioactive source and emitted X-rays. They were counted by an Ultra-LEGe detector with resolution of 150 eV at 5.9 keV. For pure elements results have been compared with the theoretical calculated values. According to our results band length and mutual interaction of atoms affected the results. We claimed that these effects would help researchers who study on superconductors, especially determining which compound can be show the superconductor properties.     

Characterization and source term assessments of radioactive particles from Marshall Islands using non-destructive analytical techniques

Six plutonium-containing particles stemming from Runit Island soil (Marshall Islands) were characterized by non-destructive analytical and microanalytical methods. Composition and elemental distribution in the particles were studied with synchrotron radiation based micro X-ray fluorescence spectrometry. Scanning electron microscope equipped with energy dispersive X-ray detector and with wavelength dispersive system as well as a secondary ion mass spectrometer were used to examine particle surfaces. Based on the elemental composition the particles were divided into two groups: particles with pure Pu matrix, and particles where the plutonium is included in Si/O-rich matrix being more heterogenously distributed. All of the particles were identified as nuclear fuel fragments of exploded weapon components. As containing plutonium with low ²⁴⁰Pu/²³⁹Pu atomic ratio, less than 0.065, which corresponds to weapons-grade plutonium or a detonation with low fission yield, the particles were identified to originate from the safety test and low-yield tests conducted in the history of Runit Island. The Si/O-rich particles contained traces of ¹³⁷Cs (^239 + 240Pu/¹³⁷Cs activity ratio higher than 2500), which indicated that a minor fission process occurred during the explosion. The average ²⁴¹Am/²³⁹Pu atomic ratio in the six particles was 3.7 × 10^− 3 ± 0.2 × 10^− 3 (February 2006), which indicated that plutonium in the different particles had similar age.     

Characterisation of rotary kiln residues from the pyrolysis of shredder residues: Issues with lead

Stringent legislation is being to be implemented across Europe relating to heavy metal contamination into the environment. This study thus focuses on developing a method for reliably determining the lead content of automotive shredder residue (ASR). The material is first pyrolysed to remove organic fractions. Different analytical methods were then used to investigate the concentrations of heavy metals in the burned char, which varies from chunks of metals in larger sized fractions to fine powders of mostly non-metals. By considering results from ICP-MS, EDXRF, WDXRF and a portable EDXRF, it was found that varying values were obtained but that consistent ‘consensus values’ could be determined. Such ‘consensus’ values of lead, copper, iron and zinc are thus reported, and show that properly depolluted ELVs have significantly lower lead levels than normal shredder residue (SR) feed −8000 ppm versus 16,000 ppm. The finest fraction, <850 μm, makes up around half of the mass of the SR and has only 2700 ppm and 5400 ppm lead concentration values for depolluted ELVs and normal SR, respectively, making it of interest for further work to develop uses as a feed in other industries.     

The investigations on K and L X-ray fluorescence parameters of gold compounds

The study aimed to determine the chemical effects on the K and L X-ray intensity ratios and the K and L X-ray production cross sections for gold compounds. The K shell fluorescence yields and L shell average yields were also investigated. The samples were excited by 59.5 keV γ-rays from an ²⁴¹Am annular radioactive source and 123.6 keV γ-rays from a ⁵⁷Co annular radioactive source. K and L X-rays emitted from samples were counted by an Ultra-LEGe detector with a resolution of 0.150 keV at 5.9 keV. The experimental values were compared with theoretical, the semi-empirical and other experimental values.     

(Liquid + liquid) equilibria of (water + linalool + limonene) ternary system at T = (298.15, 308.15, and 318.15) K

(Liquid + liquid) equilibrium (LLE) data for {water (1) + linalool (2) + limonene (3)} ternary system at T = (298.15, 308.15, and 318.15 ± 0.05) K are reported. The organic chemicals were quantified by gas chromatography using a flame ionisation detector while water was quantified using a thermal conductivity detector. The effect of the temperature on (liquid + liquid) equilibrium is determined and discussed. Experimental data for the ternary mixture are compared with values calculated by the NRTL and UNIQUAC equations, and predicted by means of the UNIFAC group contribution method. It is found that the UNIQUAC and NRTL models provide a good correlation of the solubility curve at these three temperatures, while comparing the calculated values with the experimental ones, the best fit is obtained with the NRTL model. Finally, the UNIFAC model provides poor results, since it predicts a greater heterogeneous region than experimentally observed.     

Traditional Vinegars Identification by Colorimetric Sensor

An expanded colorimetric array detector that was capable of the highly sensitive and highly selective discrimination of vinegars was developed. The system of olfaction visualization and operational approach were discussed. Thirty dyes were selected from natural dyes, chemoresponsive dyes and pH dyes. A 5 × 6 colorimetric sensor array was created by printing the dyes on reverse phase silica gel plates. Four traditional vinegars were measured by the colorimetric sensor array. With cluster analysis, all samples were assembled ‘Zhenjiang Vinegar’, ‘Shanxi Vinegar’, ‘Sichuan Vinegar’, ‘Jiangzhe Vinegar’ when the similarity was 12. This work showed the potential applications of the olfaction visualization technology for visual analyzing and fingerprint identifying the aroma of food.     

Study on distribution of elements in deep-sea Pacific polymetallic nodules via two-dimensional mapping laser ionization orthogonal time-of-flight mass spectrometry

A newly developed two-dimensional mapping high irradiance laser ionization orthogonal time-of-flight mass spectrometer (LI-O-TOFMS) has been applied for the elemental mapping of polymetallic nodules. Two polymetallic nodule standards were used to demonstrate the efficacy of LI-O-TOFMS for the standardless semiquantitative analysis and the spatial distribution of elements in a deep-sea Pacific polymetallic nodule was mapped. It was found that the two groups of elements, Mn–Ni–Cu–Fe and Co–Si–Al, show clear element-dependent spatial relationships. It is hypothesized that these spatial distributions reflect the environmental and physico-chemical conditions during the nodule formation. LI-O-TOFMS is shown to be a powerful tool in elemental analysis of polymetallic nodules, with the detection limits down to 10^− 7 g/g and a dynamic range of 7 orders of magnitude. Based on the images acquired, the contents of elements and their relationships can be revealed visually.     

X-ray micro-imaging by capillary optics

In this work the results on X-ray micro-imaging by means of novel polycapillary optical elements will be presented. To simulate various radiation propagation processes in both single capillary and polycapillary systems, a PolyCAD code was developed. The new experimental results on radiation redistribution by novel capillary lenses in comparison with simulated data will be reported. The images of characterized extended samples (~ 3 mm) were recorded with 6 μm resolution, the maximum provided by CCD. Polycapillary Optics CAD software X-ray tracing Imaging Confocal 02.60.Cb 02.70.-c 41.50. + h 42.15.-i 42.15.Dp 42.30.-d.     

Rapidly renewable silver amalgam annular band electrode for voltammetry and polarography

This work describes a novel type of working electrode for use in voltammetry and polarography — the renewable silver liquid amalgam film–modified silver solid amalgam annular band electrode (AgLAF–AgSAE). The electrode is produced by mechanically refreshing the silver liquid amalgam film (AgLAF) before each measurement. The main constituents of the electrode are: a specially constructed silver solid amalgam annular band electrode (AgSAE), two silicon O-rings, silver liquid amalgam and a polypropylene electrode body. Contaminants from the analyzed solution are removed and the AgSAE surface is covered with a thick layer of fresh amalgam while pulling the AgSAE into the sensor body. During movement in the reverse direction AgLAF is formed and homogenized. The time needed to refresh the film is less than 1 s. The electrode is characterized by excellent surface repeatability (～ 1%) and long-term stability (over ten thousand measurement cycles).     

Determining mineral elements in four kinds of grains from Beijing market by ICP-MS simultaneously

Mineral elements are essential components for human health from food, but their contents in wheat, millet, corn and soybean have not been compared. Contents of mineral elements in wheat, millet, corn and soybean from Beijing market of China were detected by ICP-MS. The RSDs (relative standard deviation) range from 0.85% to 3.52% and the detecting limits range from 0.13 to 0.85 μg/L, which showed that this method is accurate and precise to detect mineral elements in grains simultaneously. The data showed that (1) ICP-MS is a simple and precise method to determine many mineral elements in grains simultaneously. (2) Elements followed by descending order in four grains are usually K > Mg > Ca > Fe > Zn > Mn > Cu > Mo > Li, and grains arranged in order from high to low levels of mineral elements are usually soybean > millet > wheat ≈ corn. So we should take in more minor grains, such as soybean and millet on daily diet.     

Electrothermal vaporization coupled with inductively coupled plasma array–detector mass spectrometry for the multielement analysis of Al2O3 ceramic powders

An electrothermal vaporization (ETV) system useful for the analysis of solutions and slurries has been coupled with a sector-field inductively coupled plasma mass spectrometer (ICP–MS) equipped with an array detector. The ability of this instrument to record the transient signals produced for a number of analytes in ETV–ICP–MS is demonstrated. Detection limits for Mn, Fe, Co, Ni, Cu, Zn and Ga are in the range of 4–60 pg μL^− 1 for aqueous solutions and in the low μg g^− 1 range for the analysis of 10 mg mL^− 1 slurries of Al₂O₃ powders. The dynamic ranges measured for Fe, Cu and Ga spanned 3–5 orders of magnitude when the detector was operated in the low-gain mode and appear to be limited by the ETV system. Trace amounts of Fe, Cu and Ga could be directly determined in Al₂O₃ powders at the 2–270 μg g^− 1 level without the use of thermochemical reagents. The results well agree with literature values for Fe and Cu, whereas deviations of 50% at the 90 μg g^− 1 level for Ga were found.