A sagittally focusing double‐multilayer monochromator for ultrafast X‐ray imaging applications

The development of a sagittally focusing double‐multilayer monochromator is reported, which produces a spatially extended wide‐bandpass X‐ray beam from an intense synchrotron bending‐magnet source at the Advanced Photon Source, for ultrafast X‐ray radiography and tomography applications. This monochromator consists of two W/B₄C multilayers with a 25 Å period coated on Si single‐crystal substrates. The second multilayer is mounted on a sagittally focusing bender, which can dynamically change the bending radius of the multilayer in order to condense and focus the beam to various points along the beamline. With this new apparatus, it becomes possible to adjust the X‐ray beam size to best match the area detector size and the object size to facilitate more efficient data collection using ultrafast X‐ray radiography and tomography.     

Confocal full‐field X‐ray microscope for novel three‐dimensional X‐ray imaging

A confocal full‐field X‐ray microscope has been developed for use as a novel three‐dimensional X‐ray imaging method. The system consists of an X‐ray illuminating `sheet‐beam' whose beam shape is micrified only in one dimension, and an X‐ray full‐field microscope whose optical axis is normal to the illuminating sheet beam. An arbitral cross‐sectional region of the object is irradiated by the sheet‐beam, and secondary X‐ray emission such as fluorescent X‐rays from this region is imaged simultaneously using the full‐field microscope. This system enables a virtual sliced image of a specimen to be obtained as a two‐dimensional magnified image, and three‐dimensional observation is available only by a linear translation of the object along the optical axis of the full‐field microscope. A feasibility test has been carried out at beamline 37XU of SPring‐8. Observation of the three‐dimensional distribution of metallic inclusions in an artificial diamond was performed.     

X‐ray fluorescence spectroscopy and Monte Carlo simulation for quantitative characterization of Bolivian pre‐Hispanic golden artefacts

The quantification of archaeological artefacts with X‐ray Fluorescence is quite complex because it demands some calibration procedure. It is also rather more challenging when the customization of the portable equipment for in situ measurements is required. The objective of this study was to introduce a quantitative method by performing a calibration curve for a ternary gold alloy (Au, Ag and Cu). Fast Monte Carlo simulation combined with in situ portable XRF (pXRF) measurements in order to circumvent the calibration requirement using standard reference materials was used. Measurements with a laboratory‐made equipment were taken from a set of 16 pre‐hispanic gold alloy artefacts of a collection from the Museo Nacional de Etnografia y Folklore, La Paz, Bolivia. The spectra simulation was conducted with the XMI‐MSIM software.The results demonstrated that the combined use of pXRF measurements and spectra simulation via Monte Carlo is a feasible method for gold alloy quantification. In the examined samples, the Cu content was below 5% and for Au it ranged from 13 to 100% . Moreover, some peculiarities of the artefacts archaeological context were discussed.     

Monte Carlo simulation code for confocal 3D micro‐beam X‐ray fluorescence analysis of stratified materials

Stratified materials are of great importance for many branches of modern industry, e.g. electronics or optics and for biomedical applications. Examination of chemical composition of individual layers and determination of their thickness helps to get information on their properties and function. A confocal 3D micro X‐ray fluorescence (3D µXRF) spectroscopy is an analytical method giving the possibility to investigate 3D distribution of chemical elements in a sample with spatial resolution in the micrometer regime in a non‐destructive way. Thin foils of Ti, Cu and Au, a bulk sample of Cu and a three‐layered sandwich sample, made of two thin Fe/Ni alloy foils, separated by polypropylene, were used as test samples. A Monte Carlo (MC) simulation code for the determination of elemental concentrations and thickness of individual layers in stratified materials with the use of confocal 3D µXRF spectroscopy was developed. The X‐ray intensity profiles versus the depth below surface, obtained from 3D µXRF experiments, MC simulation and an analytical approach were compared. Correlation coefficients between experimental versus simulated, and experimental versus analytical model X‐ray profiles were calculated. The correlation coefficients were comparable for both methods and exceeded 99%. The experimental X‐ray intensity profiles were deconvoluted with iterative MC simulation and by using analytical expression. The MC method produced slightly more accurate elemental concentrations and thickness of successive layers as compared to the results of the analytical approach. This MC code is a robust tool for simulation of scanning confocal 3D µXRF experiments on stratified materials and for quantitative interpretation of experimental results. Copyright © 2011 John Wiley & Sons, Ltd.     

Chemical speciation via X‐ray emission spectra

Since the early days of X‐ray spectrometry, X‐ray emission and fluorescence spectra have been used to investigate chemical speciation, e.g. the dependence on the formal oxidation state. Laboratory wavelength‐dispersive spectrometers have adequate resolution for these measurements. However, almost all studies have employed empirical methods to interpret the spectra. We aim to place such methods on a quantitative basis by means of efficient ab initio calculations of the X‐ray emission line shapes based on a self‐consistent, real‐space Green's function approach, as implemented in the X‐ray spectroscopy code FEFF8.2. Calculations are presented for the phosphorus K‐M_{2, 3}, and the chromium L‐series emission lines for a selection of simple compounds. These lines exhibit changes depending on the oxidation state and on the neighboring atoms in the compounds that can be observed with instruments available in many XRF laboratories. The calculated spectra, as modified by convolution with a model monochromator response function, are compared with measured spectra. Simulated and measured spectra are found to be in reasonable agreement, and show that the approach has the potential to yield quantitative information about the chemical state. Copyright © 2006 John Wiley & Sons, Ltd.     

Experimental study of the efficiency of a SDD X‐ray detector by means of PIXE spectra

The efficiency of a silicon drift detector with ultrathin window was studied for energies between 0.27 and 25 keV. Experimental values of the X‐ray yields from samples of known stoichiometry were obtained by impact of 2 MeV protons. By using theoretical calculations of these yields the relative efficiency of the detector was evaluated. The results are compared with efficiency values obtained from the window transmission and the detector quantum efficiency. A quantitative analysis of a particle induced X‐ray emission spectrum for a reference sample was performed in order to evaluate the consistency of the data presented in this work. Copyright © 2013 John Wiley & Sons, Ltd.     

X‐ray grating interferometer for biomedical imaging applications at Shanghai Synchrotron Radiation Facility

An X‐ray grating interferometer was installed at the BL13W beamline of Shanghai Synchrotron Radiation Facility (SSRF) for biomedical imaging applications. Compared with imaging results from conventional absorption‐based micro‐computed tomography, this set‐up has shown much better soft tissue imaging capability. In particular, using the set‐up, the carotid artery and the carotid vein in a formalin‐fixed mouse can be visualized in situ without contrast agents, paving the way for future applications in cancer angiography studies. The overall results have demonstrated the broad prospects of the existing set‐up for biomedical imaging applications at SSRF.     

Recording X‐ray spectra with an audio digitizer

X‐ray spectra were recorded with a notebook computer and analyzed by software on the computer, without a pulse height analyzer (PHA) or a digital signal processor (DSP). An audio (microphone or line) input on a personal computer has a built‐in analogue‐to‐digital converter (ADC) for digital audio recording. The output signal of the X‐ray detector is recorded through the audio input of the computer and then analyzed by software on the computer. On the basis of this method, X‐rays from a radium source were measured with a cadmium telluride detector. K X‐rays of bismuth were detected. Full width at half maximum (FWHM) was 5.6 keV at Kα of bismuth (77.1 keV), enough to separate Kβ (87.3 keV) from Kα of bismuth. The present method achieved almost equal energy resolution as that of the regular method (5.3 keV FWHM at 77.1 keV). Copyright © 2010 John Wiley & Sons, Ltd.     

Correcting for surface topography in X‐ray fluorescence imaging

Samples with non‐planar surfaces present challenges for X‐ray fluorescence imaging analysis. Here, approximations are derived to describe the modulation of fluorescence signals by surface angles and topography, and suggestions are made for reducing this effect. A correction procedure is developed that is effective for trace element analysis of samples having a uniform matrix, and requires only a fluorescence map from a single detector. This procedure is applied to fluorescence maps from an incised gypsum tablet.     

Coherent X‐ray diffractive imaging of protein crystals

The technique of coherent X‐ray diffraction imaging (CXDI) has recently shown great promise for the study of inorganic nanocrystals. In this work the CXDI method has been applied to the study of micrometer‐size protein crystals. Finely sampled diffraction patterns of single crystals were measured and iterative phase‐retrieval algorithms were used to reconstruct the two‐dimensional shape of the crystal. The density maps have limited reproducibility because of radiation damage, but show clear evidence for crystal facets. Qualitative analysis of a number of single‐crystal diffraction peaks indicates the presence of inward surface contraction on 2 µm size crystals. A survey of several hundred diffraction patterns yielded a number of examples with dramatic single‐sided streaks, for which a plausible model is constructed.     

A soft X‐ray beamline for transmission X‐ray microscopy at ALBA

The MISTRAL beamline is one of the seven phase‐I beamlines at the ALBA synchrotron light source (Barcelona, Spain) that will be opened to users at the end of 2010. MISTRAL will be devoted to cryotomography in the water window and multi‐keV spectral regions for biological applications. The optics design consists of a plane‐grating monochromator that has been implemented using variable‐line‐spacing gratings to fulfil the requirements of X‐ray microscopy using a reflective condenser. For instance, a fixed‐focus condition independent of the included angle, constant magnification as well as coma and spherical aberration corrections are achieved with this system. The reported design is of wider use.     

A tunable wedge‐shaped absorber for hard X‐ray synchrotron applications

The concept of a concave aluminium wedge‐shaped absorber for hard X‐ray synchrotron beamlines is presented. Unlike the commonly used absorber types (fixed‐thickness absorber sheets or binary exchangers of individual fixed absorbers), this concept allows a compact system, controlled with a single linear positioner, and provides a wide attenuation range as well as a precise tunability over a large energy range. Data were recorded at the Nanofocus Endstation of the MINAXS beamline, PETRA III, Hamburg, Germany.     

Analysis of engine motor oils by X‐ray absorption and X‐ray fluorescence spectroscopies

The molecular structure of lubricating motor oils is investigated by X‐ray absorption fine structure spectroscopy measurements. Both fresh and used oils are studied. Although the Zn K‐edge spectra gave information about the degradation of the antiwear/antioxidant zinc dialkyl dithiophosphate (ZDDP) additives within the oil, Fe K‐edge spectra are representatives for iron species dispersed in the oil during operation at elevated temperatures and pressures in the engine. The detailed analysis of the measured data shows that substantial differences are detectable in the spectra of the fresh and used oil. Our results show that the Zn–S bonds of the ZDDP are decomposed during the operation, resulting in Zn–O bonds instead. Furthermore, sixfold Fe–O bonds similar to those in Fe₂O₃ are found within the used oil, suggesting the presence of debris from the antiwear film of lubricated motor parts in the used oil. Copyright © 2014 John Wiley & Sons, Ltd.     

Utilizing broadband X‐rays in a Bragg coherent X‐ray diffraction imaging experiment

A method is presented to simplify Bragg coherent X‐ray diffraction imaging studies of complex heterogeneous crystalline materials with a two‐stage screening/imaging process that utilizes polychromatic and monochromatic coherent X‐rays and is compatible with in situ sample environments. Coherent white‐beam diffraction is used to identify an individual crystal particle or grain that displays desired properties within a larger population. A three‐dimensional reciprocal‐space map suitable for diffraction imaging is then measured for the Bragg peak of interest using a monochromatic beam energy scan that requires no sample motion, thus simplifying in situ chamber design. This approach was demonstrated with Au nanoparticles and will enable, for example, individual grains in a polycrystalline material of specific orientation to be selected, then imaged in three dimensions while under load.     

Characterisation of a megavoltage linear accelerator Bremsstrahlung by means of Monte Carlo simulations

This work presents a method for megavoltage X‐ray Bremsstrahlung assessment by means of Monte Carlo (MC) (PENELOPE) simulations. The proposed method provides suitable spectrum characterisation by means of a few parameters, namely the acceleration potential and incident angle of electron beam on the anode. The obtained spectra have been used as incident beam for in‐depth dose distribution determination with the aim of performing further comparisons with experimental data. This comparison procedure has been employed for Bremsstrahlung assessment optimisation. Once the Linac Bremsstrahlung is well established, it may be used as incident beam for further dosimetric purposes, such as spatial dose distribution calculations. The whole process has been applied for the characterisation of the megavoltage Bremsstrahlung from a typical Linac, namely the 10 MV Varian Clinac 18. The obtained results for in‐depth dose distributions, when compared with experimental measurements, show an overall good agreement, which may suggest the feasibility of the method. Copyright © 2010 John Wiley & Sons, Ltd.     

Guiding synchrotron X‐ray diffraction by multimodal video‐rate protein crystal imaging

Synchronous digitization, in which an optical sensor is probed synchronously with the firing of an ultrafast laser, was integrated into an optical imaging station for macromolecular crystal positioning prior to synchrotron X‐ray diffraction. Using the synchronous digitization instrument, second‐harmonic generation, two‐photon‐excited fluorescence and bright field by laser transmittance were all acquired simultaneously with perfect image registry at up to video‐rate (15 frames s^?1). A simple change in the incident wavelength enabled simultaneous imaging by two‐photon‐excited ultraviolet fluorescence, one‐photon‐excited visible fluorescence and laser transmittance. Development of an analytical model for the signal‐to‐noise enhancement afforded by synchronous digitization suggests a 15.6‐fold improvement over previous photon‐counting techniques. This improvement in turn allowed acquisition on nearly an order of magnitude more pixels than the preceding generation of instrumentation and reductions of well over an order of magnitude in image acquisition times. These improvements have allowed detection of protein crystals on the order of 1 µm in thickness under cryogenic conditions in the beamline. These capabilities are well suited to support serial crystallography of crystals approaching 1 µm or less in dimension.     

X‐ray tube spectral measurement method for quantitative analysis of X‐ray fluorescence analysis

Lα and Lβ X‐ray fluorescence spectra of a lead metallic sheet were measured using an energy dispersive X‐ray spectrometer by changing the X‐ray tube voltage and the material of the primary filter. The Lα to Lβ intensity ratio changed from Lα: Lβ = 3: 1 at 15 kV to Lα: Lβ = 1: 1 at 50 kV depending on the X‐ray tube voltage and the filter. The scattered X‐ray spectra of an acrylic slab instead of the sample in the sample holder were measured by changing the applied voltage and the material of the primary filter. The calculated values of the Pb Lα/Lβ intensity ratio of the metallic sheet using the Shiraiwa–Fujino formula by inserting the scattered X‐ray spectra of an acrylic plate as incident X‐ray spectra and the fundamental parameters taken from the Elam database were in good agreement with the experimental ones. We conclude that we can obtain an incident X‐ray spectrum approximately by measuring the scattered X‐ray spectrum without measuring the direct incident beam. Copyright © 2010 John Wiley & Sons, Ltd.     

Quick X‐ray reflectivity using monochromatic synchrotron radiation for time‐resolved applications

A new technique for the parallel collection of X‐ray reflectivity (XRR) data, compatible with monochromatic synchrotron radiation and flat substrates, is described and applied to the in situ observation of thin‐film growth. The method employs a polycapillary X‐ray optic to produce a converging fan of radiation, incident onto a sample surface, and an area detector to simultaneously collect the XRR signal over an angular range matching that of the incident fan. Factors determining the range and instrumental resolution of the technique in reciprocal space, in addition to the signal‐to‐background ratio, are described in detail. This particular implementation records ～5° in 2gθ and resolves Kiessig fringes from samples with layer thicknesses ranging from 3 to 76 nm. The value of this approach is illustrated by showing in situ XRR data obtained with 100 ms time resolution during the growth of epitaxial La_0.7Sr_0.3MnO₃ on SrTiO₃ by pulsed laser deposition at the Cornell High Energy Synchrotron Source (CHESS). Compared with prior methods for parallel XRR data collection, this is the first method that is both sample‐independent and compatible with the highly collimated, monochromatic radiation typical of third‐generation synchrotron sources. Further, this technique can be readily adapted for use with laboratory‐based sources.     

Quantitative elemental analysis of individual particles with the use of micro‐beam X‐ray fluorescence method and Monte Carlo simulation

The aim of the work was to develop a Monte Carlo (MC) method and combine it with micro‐beam X‐ray fluorescence (XRF) technique for determination of chemical composition of individual particles. A collection of glass micro‐spheres, made of NIST (National Institute of Standards and Technoly) K3089 material of known chemical composition, with diameters in the range of 25–45 µm was investigated. The micro‐spheres were measured in a scanning micro‐beam XRF spectrometer utilising X‐ray tube as a source of primary radiation. Results obtained for low Z elements showed high dependence on particle size. It was found that the root mean square of concentration uncertainty, for the all elements present in the particle, increases with growing sample size. More accurate results were obtained for high Z elements such as Fe–Pb, as compared to others. The elemental percentage uncertainty did not exceed 14% for any particular sample and 6% for the whole group of the measured micro‐spheres as an average. Results obtained by the Monte Carlo method were compared with other analytical approaches. Copyright © 2009 John Wiley & Sons, Ltd.