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Sample records for synchrotron powder diffraction

  1. Synchrotron powder diffraction on Aztec blue pigments

    International Nuclear Information System (INIS)

    Sanchez del Rio, M.; Gutierrez-Leon, A.; Castro, G.R.; Rubio-Zuazo, J.; Solis, C.; Sanchez-Hernandez, R.; Robles-Camacho, J.; Rojas-Gaytan, J.

    2008-01-01

    Some samples of raw blue pigments coming from an archaeological rescue mission in downtown Mexico City have been characterized using different techniques. The samples, some recovered as a part of a ritual offering, could be assigned to the late Aztec period (XVth century). The striking characteristic of these samples is that they seem to be raw pigments prior to any use in artworks, and it was possible to collect a few μg of pigment after manual grain selection under a microscopy monitoring. All pigments are made of indigo, an organic colorant locally known as anil or xiuhquilitl. The colorant is always found in combination with an inorganic matrix, studied by powder diffraction. In one case the mineral base is palygorskite, a rare clay mineral featuring micro-channels in its structure, well known as the main ingredient of the Maya blue pigment. However, other samples present the minerals sepiolite (a clay mineral of the palygorskite family) and calcite. Another sample contains barite, a mineral never reported in prehispanic paints. We present the results of characterization using high resolution powder diffraction recorded at the European Synchrotron Radiation Facility (BM25A, SpLine beamline) complemented with other techniques. All of them gave consistent results on the composition. A chemical test on resistance to acids was done, showing a high resistance for the palygorskite and eventually sepiolite compounds, in good agreement with the excellent resistance of the Maya blue. (orig.)

  2. High resolution Neutron and Synchrotron Powder Diffraction

    International Nuclear Information System (INIS)

    Hewat, A.W.

    1986-01-01

    The use of high-resolution powder diffraction has grown rapidly in the past years, with the development of Rietveld (1967) methods of data analysis and new high-resolution diffractometers and multidetectors. The number of publications in this area has increased from a handful per year until 1973 to 150 per year in 1984, with a ten-year total of over 1000. These papers cover a wide area of solid state-chemistry, physics and materials science, and have been grouped under 20 subject headings, ranging from catalysts to zeolites, and from battery electrode materials to pre-stressed superconducting wires. In 1985 two new high-resolution diffractometers are being commissioned, one at the SNS laboratory near Oxford, and one at the ILL in Grenoble. In different ways these machines represent perhaps the ultimate that can be achieved with neutrons and will permit refinement of complex structures with about 250 parameters and unit cell volumes of about 2500 Angstrom/sp3/. The new European Synchotron Facility will complement the Grenoble neutron diffractometers, and extend the role of high-resolution powder diffraction to the direct solution of crystal structures, pioneered in Sweden

  3. Towards microstrip detectors for synchrotron powder diffraction facilities

    CERN Document Server

    Fauth, F; Auderset, H; Maehlum, G; Pattison, P; Patterson, B

    2000-01-01

    A major improvement of todays experimental techniques in powder diffraction can be achieved by using a massively parallel detection of diffraction patterns with arrays of solid-state detectors. In order to determine the feasibility of this technique, a test experiment was performed at the Swiss-Norwegian Beamline (SNBL) of the European Synchrotron Radiation Facility (ESRF). Diffraction patterns of previously characterized samples were first recorded with conventional equipment: in high-intensity mode with a single slit in front of the detector (Debye-Scherrer geometry) and at highest angular resolution with an analyzer crystal before the detector. Results were then compared to measurements performed with a double-sided silicon microstrip detector. Particular attention was placed on angular resolution and integrated intensities since these parameters are of most importance for structure determination from powder diffraction patterns. The results presented in this paper provide a basis for the design of a dedic...

  4. New synchrotron powder diffraction facility for long-duration experiments.

    Science.gov (United States)

    Murray, Claire A; Potter, Jonathan; Day, Sarah J; Baker, Annabelle R; Thompson, Stephen P; Kelly, Jon; Morris, Christopher G; Yang, Sihai; Tang, Chiu C

    2017-02-01

    A new synchrotron X-ray powder diffraction instrument has been built and commissioned for long-duration experiments on beamline I11 at Diamond Light Source. The concept is unique, with design features to house multiple experiments running in parallel, in particular with specific stages for sample environments to study slow kinetic systems or processes. The instrument benefits from a high-brightness X-ray beam and a large area detector. Diffraction data from the commissioning work have shown that the objectives and criteria are met. Supported by two case studies, the results from months of measurements have demonstrated the viability of this large-scale instrument, which is the world's first dedicated facility for long-term studies (weeks to years) using synchrotron radiation.

  5. Synchrotron radiation X-ray powder diffraction techniques applied in hydrogen storage materials - A review

    OpenAIRE

    Honghui Cheng; Chen Lu; Jingjing Liu; Yongke Yan; Xingbo Han; Huiming Jin; Yu Wang; Yi Liu; Changle Wu

    2017-01-01

    Synchrotron radiation is an advanced collimated light source with high intensity. It has particular advantages in structural characterization of materials on the atomic or molecular scale. Synchrotron radiation X-ray powder diffraction (SR-XRPD) has been successfully exploited to various areas of hydrogen storage materials. In the paper, we will give a brief introduction on hydrogen storage materials, X-ray powder diffraction (XRPD), and synchrotron radiation light source. The applications of...

  6. Crystal structure of lead uranyl carbonate mineral widenmannite: Precession electron-diffraction and synchrotron powder-diffraction study

    Czech Academy of Sciences Publication Activity Database

    Plášil, J.; Palatinus, L.; Rohlíček, J.; Houdková, L.; Klementová, Mariana; Goliáš, V.; Škácha, P.

    2014-01-01

    Roč. 99, 2-3 (2014), s. 276-282 ISSN 0003-004X Institutional support: RVO:61388980 Keywords : Widenmannite * uranyl bicarbonate * crystal structure * precession electron diffraction * synchrotron powder diffraction Subject RIV: CA - Inorganic Chemistry Impact factor: 1.964, year: 2014

  7. Synchrotron radiation X-ray powder diffraction techniques applied in hydrogen storage materials - A review

    Directory of Open Access Journals (Sweden)

    Honghui Cheng

    2017-02-01

    Full Text Available Synchrotron radiation is an advanced collimated light source with high intensity. It has particular advantages in structural characterization of materials on the atomic or molecular scale. Synchrotron radiation X-ray powder diffraction (SR-XRPD has been successfully exploited to various areas of hydrogen storage materials. In the paper, we will give a brief introduction on hydrogen storage materials, X-ray powder diffraction (XRPD, and synchrotron radiation light source. The applications of ex situ and in situ time-resolved SR-XRPD in hydrogen storage materials, are reviewed in detail. Future trends and proposals in the applications of the advanced XRPD techniques in hydrogen storage materials are also discussed.

  8. Powder Diffraction

    Science.gov (United States)

    Hart, Michael

    The importance of x-ray powder diffraction as an analytical tool for phase identification of materials was first pointed out by Debye and Scherrer1,2 in Germany and, quite independently, by Hull3,4 in the United States of America. Three distinct periods of evolution lead to ubiquitous application in many fields of science and technology. In the, first period, until the- mid-1940's. applications were and developed covering broad categories of materials including inorganic materials, minerals, cerarffics, metals, alloys, organic materials and polymers. During this formative period, the concept of quantitative phase analysis was demonstrated5. In the second period there followed the blossoming of technology and commercial instruments became widely used. The history is well summarized by Parrish6 and by Langford and Loudr7. By 1980 there were probably 10000 powder diffractometers in routine use, making it the most widely used of all x-ray crystallographic instruments. In the third, present, period data bases became firmly established and sophisticated pattern fitting and recognition software made many aspects of powder diffraction analysis routine. High resolution, tunable powder diffractometers were developed at sources of synchrotron radiation8-10. The tunability of the spectrum made it possible to exploit all the subtleties of x-ray spectroscopy in diffraction experiments11.

  9. Powder diffraction

    Energy Technology Data Exchange (ETDEWEB)

    Hart, M.

    1995-12-31

    the importance of x-ray powder diffraction as an analytical tool for phase identification of materials was first pointed out by Debye and Scherrer in Germany and, quite independently, by Hull in the US. Three distinct periods of evolution lead to ubiquitous application in many fields of science and technology. In the first period, until the mid-1940`s, applications were and developed covering broad categories of materials including inorganic materials, minerals, ceramics, metals, alloys, organic materials and polymers. During this formative period, the concept of quantitative phase analysis was demonstrated. In the second period there followed the blossoming of technology and commercial instruments became widely used. The history is well summarized by Parrish and by Langford and Loueer. By 1980 there were probably 10,000 powder diffractometers in routine use, making it the most widely used of all x-ray crystallographic instruments. In the third, present, period data bases became firmly established and sophisticated pattern fitting and recognition software made many aspects of powder diffraction analysis routine. High resolution, tunable powder diffractometers were developed at sources of synchrotron radiation. The tunability of the spectrum made it possible to exploit all the subtleties of x-ray spectroscopy in diffraction experiments.

  10. Powder diffraction

    International Nuclear Information System (INIS)

    Hart, M.

    1995-01-01

    The importance of x-ray powder diffraction as an analytical tool for phase identification of materials was first pointed out by Debye and Scherrer in Germany and, quite independently, by Hull in the US. Three distinct periods of evolution lead to ubiquitous application in many fields of science and technology. In the first period, until the mid-1940's, applications were and developed covering broad categories of materials including inorganic materials, minerals, ceramics, metals, alloys, organic materials and polymers. During this formative period, the concept of quantitative phase analysis was demonstrated. In the second period there followed the blossoming of technology and commercial instruments became widely used. The history is well summarized by Parrish and by Langford and Loueer. By 1980 there were probably 10,000 powder diffractometers in routine use, making it the most widely used of all x-ray crystallographic instruments. In the third, present, period data bases became firmly established and sophisticated pattern fitting and recognition software made many aspects of powder diffraction analysis routine. High resolution, tunable powder diffractometers were developed at sources of synchrotron radiation. The tunability of the spectrum made it possible to exploit all the subtleties of x-ray spectroscopy in diffraction experiments

  11. ENDIX. A computer program to simulate energy dispersive X-ray and synchrotron powder diffraction diagrams

    International Nuclear Information System (INIS)

    Hovestreydt, E.; Karlsruhe Univ.; Parthe, E.; Benedict, U.

    1987-01-01

    A Fortran 77 computer program is described which allows the simulation of energy dispersive X-ray and synchrotron powder diffraction diagrams. The input consists of structural data (space group, unit cell dimensions, atomic positional and displacement parameters) and information on the experimental conditions (chosen Bragg angle, type of X-ray tube and applied voltage or operating power of synchrotron radiation source). The output consists of the normalized intensities of the diffraction lines, listed by increasing energy (in keV), and of an optional intensity-energy plot. The intensities are calculated with due consideration of the wave-length dependence of both the anomalous dispersion and the absorption coefficients. For a better agreement between observed and calculated spectra provision is made to optionally superimpose, on the calculated diffraction line spectrum, all additional lines such as fluorescence and emission lines and escape peaks. The different effects which have been considered in the simulation are discussed in some detail. A sample calculation of the energy dispersive powder diffraction pattern of UPt 3 (Ni 3 Sn structure type) is given. Warning: the user of ENDIX should be aware that for a successful application it is necessary to adapt the program to correspond to the actual experimental conditions. Even then, due to the only approximately known values of certain functions, the agreement between observed and calculated intensities will not be as good as for angle dispersive diffraction methods

  12. Application of new synchrotron powder diffraction techniques to anomalous scattering from glasses

    International Nuclear Information System (INIS)

    Beno, M.A.; Knapp, G.S.; Armand, P.; Price, D.L.; Saboungi, M.

    1995-01-01

    We have applied two synchrotron powder diffraction techniques to the measurement of high quality anomalous scattering diffraction data for amorphous materials. One of these methods, which uses a curved perfect crystal analyzer to simultaneously diffract multiple powder lines into a position sensitive detector has been shown to possess high resolution, low background, and very high counting rates. This data measurement technique provides excellent energy resolution while minimizing systematic errors resulting from detector nonlinearity. Anomalous scattering data for a Cesium Germanate glass collected using this technique will be presented. The second powder diffraction technique uses a flat analyzer crystal to deflect multiple diffraction lines out of the equatorial plane. Calculations show that this method possesses sufficient energy resolution for anomalous scattering experiments when a perfect crystal analyzer is used and is experimentally much simpler. Future studies will make use of a rapid sample changer allowing the scattering from the sample and a standard material (a material not containing the anomalous scatterer) to be measured alternately at each angle, reducing systematic errors due to beam instability or sample misalignment

  13. Multipole electron-density modelling of synchrotron powder diffraction data: the case of diamond

    DEFF Research Database (Denmark)

    Svendsen, H.; Overgaard, J.; Busselez, R.

    2010-01-01

    encountered in single-crystal studies of small-unit-cell inorganic structures can be overcome with synchrotron powder diffraction. It is shown that the standard Hansen-Coppens multipole model is not flexible enough to fit the static theoretical structure factors, whereas fitting of thermally smeared structure...... parameter. This directly exposes a correlation between electron density and thermal parameters even for a light atom such as carbon, and it also underlines that in organic systems proper deconvolution of thermal motion is important for obtaining correct static electron densities....

  14. In Situ High Resolution Synchrotron X-Ray Powder Diffraction Studies of Lithium Batteries

    DEFF Research Database (Denmark)

    Amri, Mahrez; Fitch, Andy; Norby, Poul

    2015-01-01

    Lithium ion battery technology is the heart in operating modern technology devices such as mobile phones and laptops. However, as our society is moving towards the utilization of sustainable energy sources, batteries can be foreseen to become an even more important part of the energy infrastructure...... materials [3]. We report results from the first in situ time resolved high resolution powder diffraction experiments at beamline ID22/31 at the European Synchrotron Radiation Facility, ESRF. We follow the structural changes during charge of commercial LiFePO4 based battery materials using the Rietveld...

  15. Characterisation of microfocused beam for synchrotron powder diffraction using a new X-ray camera

    International Nuclear Information System (INIS)

    Thomas, C; Potter, J; Tang, C C; Lennie, A R

    2012-01-01

    The powder diffraction beamline I11, Diamond Light Source, is being continually upgraded as requirements of the user community evolve. Intensities of X-rays from the I11 in-vacuum electron undulator in the 3 GeV synchrotron fall off at higher energies. By focusing higher energy X-rays, we can overcome flux limitations, and open up new diffraction experiments. Here, we describe characterisation of microfocusing using compound refractive lenses (CRL). For a relatively modest outlay, we have developed an experimental setup and a novel X-ray camera with good sensitivity and a resolution specification suitable for characterising these focusing optics. We show that vertical oscillations in the focused beam compromise resolution of the source imaged by the CRL. Nevertheless, we have measured CRL focusing properties, and demonstrate the use of energy scanning to determine lens alignment. Real benefits of the intensity gain are illustrated.

  16. Synchrotron Powder X-ray Diffraction Study of the Structure and Dehydration Behavior of Sepiolite

    Science.gov (United States)

    Post, J. E.; Bish, D. L.; Heaney, P. J.

    2006-05-01

    Sepiolite is a hydrous Mg-silicate clay mineral with fibrous morphology that typically occurs as fine-grained, poorly crystalline masses. It occurs in a wide variety of geological environments and has been mined for centuries because of its many uses, e.g. in the pharmaceutical, fertilizer, and pesticide industries. Its versatile functionality derives from the large surface area and microporosity that are characteristic of the material. In recent years, sepiolite has received considerable attention with regard to the adsorption of organics, for use as a support for catalysts, as a molecular sieve, and as an inorganic membrane for ultrafiltration. Because of its fine-grained and poorly crystalline nature, it has not been possible to study sepiolite's crystal structure using single-crystal X-ray diffraction methods, and consequently many details of the structure are still not well known. In this study, Rietveld refinements using synchrotron powder X-ray diffraction data were used to investigate the crystal structure and dehydration behavior of sepiolite from Durango, Mexico. The room- temperature (RT) sepiolite structure in air compares well with previous models but reveals an additional zeolitic water site. The RT structure under vacuum retained only ~1/8 of the zeolitic water and the volume decreased 1.3%. Real-time, temperature-resolved synchrotron powder X-ray diffraction data and Rietveld refinements were used to investigate the behavior of the sepiolite structure from 300 to 925 K. Rietveld refinements revealed that most of the zeolitic water is lost by ~390 K, accompanied by a decrease in the a and c unit-cell parameters. Above ~600 K the sepiolite structure folds as one-half of the crystallographically bound water is lost. Rietveld refinements of the "anhydrous" sepiolite structure reveal that, in general, unit-cell parameters a, b, â and volume steadily decrease with increasing temperature; there is an obvious change in slope at ~820 K suggesting a phase

  17. Simultaneous structural enhancement of powder diffraction spectra obtained by X-ray, neutron and synchrotron diffraction studies

    International Nuclear Information System (INIS)

    Maichle, J.K.

    1988-01-01

    The novel method for the enhancement of structural data is explained, and is applied for the first time for a simultaneous analysis and evaluation of neutron and synchrotron diffraction data obtained for the superconductor BaPb 0.75 Bi 0.25 O 3 . This substance can be specified in the measured temperature range between 2 K and 310 K to belong to the monoclinic space group I 2/m, and thus is determined to be in a distorted perovskite cell ahead of (a≅b≅√2 a 0 ; c≅2a 0 ). The oxygen octaeders are for the most part tilted around the (x.1/4.1/4)-axis. The simultaneous evaluation of several X-ray diffraction data sets of the high-T c superconductor YBa 2 Cu 3 O 7±z confirms the orthorhombic symmetry with space group P mmm, YBa 2 Cu 3 O 7±z likewise is in a distorted perovskite cell ahead of (a≅b≅a 0 ; c≅3a 0 ). At low temperatures, however, a saddle-shaped distortion of the oxygen group, hitherto believed to be plane, is found in the plane (x.y.0.37). (orig.) [de

  18. Parametric Powder Diffraction

    Science.gov (United States)

    David, William I. F.; Evans, John S. O.

    The rapidity with which powder diffraction data may be collected, not only at neutron and X-ray synchrotron facilities but also in the laboratory, means that the collection of a single diffraction pattern is now the exception rather than the rule. Many experiments involve the collection of hundreds and perhaps many thousands of datasets where a parameter such as temperature or pressure is varied or where time is the variable and life-cycle, synthesis or decomposition processes are monitored or three-dimensional space is scanned and the three-dimensional internal structure of an object is elucidated. In this paper, the origins of parametric diffraction are discussed and the techniques and challenges of parametric powder diffraction analysis are presented. The first parametric measurements were performed around 50 years ago with the development of a modified Guinier camera but it was the automation afforded by neutron diffraction combined with increases in computer speed and memory that established parametric diffraction on a strong footing initially at the ILL, Grenoble in France. The theoretical parameterisation of quantities such as lattice constants and atomic displacement parameters will be discussed and selected examples of parametric diffraction over the past 20 years will be reviewed that highlight the power of the technique.

  19. Synchrotron X-ray powder diffraction studies on the order-disorder phase transition in lithium ferrites

    International Nuclear Information System (INIS)

    Darul, J.; Nowicki, W.; Piszora, P.; Baehtz, C.; Wolska, E.

    2005-01-01

    Investigations on the manganese substituted lithium ferrites reveal the strong influence of manganese ions on the ordering of Li + cations in the spinel-type crystal lattice. We present the effect of Mn 3+ substitution in the LiFe 5-x Mn x O 8 (0 ≤ x ≤ 1) samples on the order-disorder phase transition and on the thermal expansion of their spinel lattices. Synchrotron X-ray measurements have been performed in the temperature range 10-300 K and 300-1173 K. The diffraction experiments were carried out at the DESY-HASYLAB high-resolution powder diffractometer (beamline B2). The transition from ordered (cubic primitive, P4 1 32) to disordered (face centred cubic, Fd3m) structure was observed with the increasing Mn 3+ content

  20. Structure of La2Cu2O5 by high-resolution synchrotron X-ray powder diffraction

    International Nuclear Information System (INIS)

    La Placa, S.J.; Bringley, J.F.; Scott, B.A.; Cox, D.E.

    1993-01-01

    Dicopper(II) dilanthanum pentaoxide, La 2 Cu 2 O 5 , M r =484.90, orthorhombic, Pbam. At T=300 K: a=5.5490(1), b=10.4774(2), c=3.8796(1) A, V=225.557(8) A 3 , Z=2, D x =7.139 g cm -3 , λ=1.2000 A. Final R I =6.20, R p =14.6 and R wp =20.61%, 124 independent reflections observed. The structure has been refined from high-resolution synchrotron X-ray powder diffraction data using the Rietveld method. It is of the oxygen-defect perovskite type and is composed entirely of corner-shared CuO 5 square pyramids, which share oxygen vacancies forming vacancy tunnels along the c axis. The La atoms reside at a perovskite-like A-site and are tenfold coordinated by oxygen. (orig.)

  1. In Situ Synchrotron Powder Diffraction Studies of Reduction-Oxidation (Redox) Behavior of Iron Ores and Ilmenite

    Science.gov (United States)

    Ilyushechkin, Alexander Y.; Kochanek, Mark; Tang, Liangguang; Lim, Seng

    2017-04-01

    Phase transformations of two types of iron-based oxides (iron ore and industrial-grade ilmenite) were studied using synchrotron powder diffraction of the samples processed in reducing and oxidizing atmospheres at 1173 K (900 °C) and 1223 K (950 °C), respectively. In iron ore oxidation, the disappearance of the wustite and fayalite phases was followed by hematite growth and a decrease of the magnetite phase. The magnetite phase was partially recovered by treatment in a reducing atmosphere. Ilmenite oxidation initiated decomposition of the ilmenite phase with rapid growth of hematite and gradual growth of the pseudobrookite phase. In a reducing atmosphere, ilmenite was gradually recovered from pseudobrookite with a relatively fast initial decrease in rutile and hematite content. Under reducing conditions, there was interaction of iron ore with magnesio-ferrites in iron ore-ash mixture and interaction of ilmenite with silica by the formation of fayalite.

  2. The crystal structures of new forms of AlF3 as determined from their synchrotron powder-diffraction patterns

    International Nuclear Information System (INIS)

    Harlow, R.L.; Herron, N.; Thorn, D.L.

    1994-01-01

    Aluminum fluoride phases are established catalysts in many classes of fluorocarbon transformations, particularly important at this time because they are key to the production of CFC alternatives. Much of what has been known about the various phases of AlF 3 , however, is open-quotes folkloreclose quotes and many of the reported phases appear to be spurious. Of the two well-characterized phases, the open-framework beta-AlF 3 has been found to be much more active than the condensed form, alpha-AlF 3 . In an effort to find new, more reliable synthetic routes to beta-AlF 3 , the pyrolysis of a variety of organic-[AlF 4 ] salts was attempted. This technique not only produced the beta-form but also a variety of new forms now designated as eta, theta, and kappa. Since these new phases were produced only in a microcrystalline state, it was not possible to characterize their structures by conventional single-crystal diffraction techniques. As a result, ab initio structural studies using synchrotron powder data were used to characterize these phases. All of the new phases consist of corner-shared AlF 6 octahedra and all contain channels. The paper details the synthesis of these new phases, the value of powder diffraction as a structural tool, and the structural relationships among the various AlF 3 phases

  3. The ab-initio crystal structure determination of UPd 2Sn by synchrotron X-ray powder diffraction

    Science.gov (United States)

    Marezio, M.; Cox, D. E.; Rossel, C.; Maple, M. B.

    1988-09-01

    The structure of the heavy-fermion compound UPd 2Sn has been determined by synchrotron x-ray radiation powder diffraction techniques. It is orthorhombic, space group Pnma [lattice parameters a = 9.9787(1), b = 4.58843(5), c = 6.89166(8) Å at room temperature] and Z = 4. All atoms, one U, one Sn, and two Pd are in 4d special positions at (x {1}/{4} z). The refinements were carried out by the Rietveld method with a pseudo-Voigt peak shape function. The final conventional R factors were: R wp = 21.3% and R E = 14.3%. The U positions in the unit cell were unequivocally located, but because of the similarity in x-ray scattering factors it was not possible to determine whether the Pd atoms and the Sn atoms are ordered or disordered on the other three sites. The structural arrangement of UPd 2Sn is of either MnCu 2Al, or ordered NaTl, or disordered Fe 3Al type, all these structures being cubic and b.c.c. related. The orthorhombic distortion is large and is probably due to a size effect of the U atoms which would be in a mixed ( {3+}/{4+}) valence state.

  4. Structure determination of Ba5AlF13 by coupling electron, synchrotron and neutron powder diffraction, solid-state NMR and ab initio calculations.

    Science.gov (United States)

    Martineau, Charlotte; Allix, Mathieu; Suchomel, Matthew R; Porcher, Florence; Vivet, François; Legein, Christophe; Body, Monique; Massiot, Dominique; Taulelle, Francis; Fayon, Franck

    2016-10-04

    The room temperature structure of Ba 5 AlF 13 has been investigated by coupling electron, synchrotron and neutron powder diffraction, solid-state high-resolution NMR ( 19 F and 27 Al) and first principles calculations. An initial structural model has been obtained from electron and synchrotron powder diffraction data, and its main features have been confirmed by one- and two-dimensional NMR measurements. However, DFT GIPAW calculations of the 19 F isotropic shieldings revealed an inaccurate location of one fluorine site (F3, site 8a), which exhibited unusual long F-Ba distances. The atomic arrangement was reinvestigated using neutron powder diffraction data. Subsequent Fourier maps showed that this fluorine atom occupies a crystallographic site of lower symmetry (32e) with partial occupancy (25%). GIPAW computations of the NMR parameters validate the refined structural model, ruling out the presence of local static disorder and indicating that the partial occupancy of this F site reflects a local motional process. Visualisation of the dynamic process was then obtained from the Rietveld refinement of neutron diffraction data using an anharmonic description of the displacement parameters to account for the thermal motion of the mobile fluorine. The whole ensemble of powder diffraction and NMR data, coupled with first principles calculations, allowed drawing an accurate structural model of Ba 5 AlF 13 , including site-specific dynamical disorder in the fluorine sub-network.

  5. Neutron powder diffraction

    International Nuclear Information System (INIS)

    David, W.I.F.

    1990-01-01

    Neutron powder diffraction is a powerful technique that provides a detailed description of moderately complex crystal structures. This is nowhere more apparent than in the area of high temperature superconductors where neutron powder diffraction has provided precise structural and magnetic information, not only under ambient conditions but also at high and low temperatures and high pressures. Outside superconductor research, the variety of materials studied by neutron powder diffraction is equally impressive including zeolites, fast ionic conductors, permanent magnets and materials undergoing phase transitions. Recent advances that include high resolution studies and real-time crystallography are presented. Future possibilities of neutron powder diffraction are discussed

  6. Simvastatin: structure solution of two new low-temperature phases from synchrotron powder diffraction and ss-NMR

    Czech Academy of Sciences Publication Activity Database

    Hušák, M.; Kratochvíl, B.; Jegorov, A.; Brus, Jiří; Maixner, J.; Rohlíček, J.

    2010-01-01

    Roč. 21, č. 3 (2010), s. 511-518 ISSN 1040-0400 R&D Projects: GA AV ČR IAA400500602; GA MŠk 2B08021 Institutional research plan: CEZ:AV0Z40500505 Keywords : crystal structure * simvastatin * powder diffraction Subject RIV: CD - Macromolecular Chemistry Impact factor: 1.727, year: 2010

  7. A crystal structure determination of PbC2O4 from synchrotron X-ray and neutron powder diffraction data

    International Nuclear Information System (INIS)

    Noerlund Christensen, A.; Cox, D.E.; Lehmann, M.S.

    1989-01-01

    The crystal structure of lead oxalate, PbC 2 O 4 , was solved ab initio from synchrotron X-ray and neutron diffraction powder patterns. The unit cell was obtained by autoindexing of Guinier film data, the basic features of the structure were solved using direct methods and integrated intensities obtained from high resolution synchrotron X-ray data, and the structure was refined by Rietveld analysis of these and high resolution neutron data. Although there were serious discrepancies in the overall profile fit of the X-ray data because of pronounced anisotropic peak broadening, the two sets of positional coordinates were in good agreement. The unit cell is triclinic, space group P1 (No.2) with lattice parameters from the synchrotron refinement: a = 555.70(1), b = 697.72(1), c = 557.26(1) pm, α = 109.554(1), β = 113.610(1), γ = 88.801(1)deg., Z = 2. The structure has two crystallographically independent oxalate ions stacked in layers alternating with layers of lead ions in the [001] direction. The oxalate ions form channels along the b axis in which the lead ions are situated in highly asymmetric coordination with seven oxygen atoms. Individual peak fits of the synchrotron data revealed all of the reflections to be broadened appreciably by comparison with the instrumental resolution. Those with scattering vectors close to the [001] axis showed an additional systematic broadening consistent with stacking faults in this direction. (author)

  8. The equation of state of PbTiO sub 3 up to 37 GPa: a synchrotron x-ray powder diffraction study

    CERN Document Server

    Sani, A; Levy, D

    2002-01-01

    High-pressure synchrotron x-ray powder diffraction patterns were collected using ID09 of ESRF (Grenoble, France) for a powder sample of PbTiO sub 3 , placed in a diamond anvil cell. The patterns were collected at room temperature using nitrogen (up to 37 GPa) and methanol-ethanol solution (up to 7 GPa) as pressure-transmitting media. The bulk moduli were calculated for the first time using the Vinet equation of state and they were compared to those of isostructural compounds. The trend of the spontaneous polarization as a function of pressure confirms that the ferroelectric-paraelectric phase transition at 11.2 GPa possesses a second-order character.

  9. Accurate Charge Densities from Powder Diffraction

    DEFF Research Database (Denmark)

    Bindzus, Niels; Wahlberg, Nanna; Becker, Jacob

    Synchrotron powder X-ray diffraction has in recent years advanced to a level, where it has become realistic to probe extremely subtle electronic features. Compared to single-crystal diffraction, it may be superior for simple, high-symmetry crystals owing to negligible extinction effects and minimal...... of conventional and novel extraction methods....

  10. Possibilities and limitations of synchrotron X-ray powder diffraction with double crystal and double multilayer monochromators for microscopic speciation studies

    Energy Technology Data Exchange (ETDEWEB)

    De Nolf, Wout [Department of Chemistry, University of Antwerp, Universiteitsplein 1, B-2610, Antwerpen (Wilrijk) (Belgium)], E-mail: wout.denolf@ua.ac.be; Jaroszewicz, Jakub [Department of Chemistry, University of Antwerp, Universiteitsplein 1, B-2610, Antwerpen (Wilrijk) (Belgium); Terzano, Roberto [Dipartimento di Biologia e Chimica Agro-forestale ed Ambientale, Via Amendola 165/A, I-70126, University of Bari, Bari (Italy); Lind, Ole Christian; Salbu, Brit [Isotope Laboratory, Norwegian University of Life Sciences, PO Box 5003, N-1432 As (Norway); Vekemans, Bart [Department of Analytical Chemistry, Ghent University, Krijgslaan 281 S12, B-9000 Gent (Belgium); Janssens, Koen [Department of Chemistry, University of Antwerp, Universiteitsplein 1, B-2610, Antwerpen (Wilrijk) (Belgium); Falkenberg, Gerald [HASYLAB at DESY, Beamline L, Notkestraat 85, D-22603, Hamburg (Germany)

    2009-08-15

    The performance of a combined microbeam X-ray fluorescence/X-ray powder diffraction (XRF/XRPD) measurement station at Hamburger Synchrotronstrahlungslabor (HASYLAB) Beamline L is discussed in comparison to that at European Synchrotron Radiation Facility (ESRF) ID18F/ID22. The angular resolution in the X-ray diffractograms is documented when different combinations of X-ray source, optics and X-ray diffraction detectors are employed. Typical angular resolution values in the range 0.3-0.5 deg. are obtained at the bending magnet source when a 'pink' beam form of excitation is employed. A similar setup at European Synchrotron Radiation Facility beamlines ID18F and ID22 allows to reach angular resolution values of 0.1-0.15 deg. In order to document the possibilities and limitations for speciation of metals in environmental materials by means of Hamburger Synchrotronstrahlungslabor Beamline L X-ray fluorescence/X-ray powder diffraction setup, two case studies are discussed, one involved in the identification of the crystal phases in which heavy metals such as chromium, iron, barium and lead are present in polluted soils of an industrial site (Val Basento, Italy) and another involved in the speciation of uranium in depleted uranium particles (Ceja Mountains, Kosovo). In the former case, the angular resolution is sufficient to allow identification of most crystalline phases present while in the latter case, it is necessary to dispose of an angular resolution of ca. 0.2 deg. to distinguish between different forms of oxidized uranium.

  11. Diffraction. Powder, amorphous, liquid

    International Nuclear Information System (INIS)

    Sosnowska, I.M.

    1999-01-01

    Neutron powder diffraction is a unique tool to observe all possible diffraction effects appearing in crystal. High-resolution neutron diffractometers have to be used in this study. Analysis of the magnetic structure of polycrystalline materials requires the use of high-resolution neutron diffraction in the range of large interplanar distances. As distinguished from the double axis diffractometers (DAS), which show high resolution only at small interplanar distances, TOF (time-of-flight) diffractometry offers the best resolution at large interplanar distances. (K.A.)

  12. Temperature-Induced Desorption of Methyl tert-Butyl Ether Confined on ZSM-5: An In Situ Synchrotron XRD Powder Diffraction Study

    Directory of Open Access Journals (Sweden)

    Elisa Rodeghero

    2017-02-01

    Full Text Available The temperature-induced desorption of methyl tert-butyl ether (MTBE from aqueous solutions onto hydrophobic ZSM-5 was studied by in situ synchrotron powder diffraction and chromatographic techniques. This kind of information is crucial for designing and optimizing the regeneration treatment of such zeolite. The evolution of the structural features monitored by full profile Rietveld refinements revealed that a monoclinic (P21/n to orthorhombic (Pnma phase transition occurred at about 100 °C. The MTBE desorption process caused a remarkable change in the unit-cell parameters. Complete MTBE desorption was achieved upon heating at about 250 °C. Rietveld analysis demonstrated that the desorption process occurred without any significant zeolite crystallinity loss, but with slight deformations in the channel apertures.

  13. In situ synchrotron powder diffraction study of the setting reaction kinetics of magnesium-potassium phosphate cements

    Czech Academy of Sciences Publication Activity Database

    Viani, Alberto; Pérez-Estébanez, Marta; Pollastri, S.; Gualtieri, A. F.

    2016-01-01

    Roč. 79, January (2016), s. 344-352 ISSN 0008-8846 R&D Projects: GA MŠk(CZ) LO1219 Keywords : kinetics * reaction * X-ray diffraction * MgO * chemically bonded ceramics Subject RIV: JN - Civil Engineering Impact factor: 4.762, year: 2016 http://www.sciencedirect.com/science/article/pii/S0008884615002690

  14. Accurate Charge Densities from Powder Diffraction

    DEFF Research Database (Denmark)

    Bindzus, Niels; Wahlberg, Nanna; Becker, Jacob

    Synchrotron powder X-ray diffraction has in recent years advanced to a level, where it has become realistic to probe extremely subtle electronic features. Compared to single-crystal diffraction, it may be superior for simple, high-symmetry crystals owing to negligible extinction effects and minimal...... peak overlap. Additionally, it offers the opportunity for collecting data on a single scale. For charge densities studies, the critical task is to recover accurate and bias-free structure factors from the diffraction pattern. This is the focal point of the present study, scrutinizing the performance...

  15. Rietveld analysis, powder diffraction and cement

    International Nuclear Information System (INIS)

    Peterson, V.

    2002-01-01

    Full text: Phase quantification of cement is essential in its industrial use, however many methods are inaccurate and/or time consuming. Powder diffraction is one of the more accurate techniques used for quantitative phase analysis of cement. There has been an increase in the use of Rietveld refinement and powder diffraction for the analysis and phase quantification of cement and its components in recent years. The complex nature of cement components, existence of solid solutions, polymorphic variation of phases and overlapping phase peaks in diffraction patterns makes phase quantification of cements by powder diffraction difficult. The main phase in cement is alite, a solid solution of tricalcium silicate. Tricalcium silicate has been found to exist in seven modifications in three crystal systems, including triclinic, monoclinic, and rhombohedral structures. Hence, phase quantification of cements using Rietveld methods usually involves the simultaneous modelling of several tricalcium silicate structures to fit the complex alite phase. An industry ordinary Portland cement, industry and standard clinker, and a synthetic tricalcium silicate were characterised using neutron, laboratory x-ray and synchrotron powder diffraction. Diffraction patterns were analysed using full-profile Rietveld refinement. This enabled comparison of x-ray, neutron and synchrotron data for phase quantification of the cement and examination of the tricalcium silicate. Excellent Rietveld fits were achieved, however the results showed that the quantitative phase analysis results differed for some phases in the same clinker sample between various data sources. This presentation will give a short introduction about cement components including polymorphism, followed by the presentation of some problems in phase quantification of cements and the role of Rietveld refinement in solving these problems. Copyright (2002) Australian X-ray Analytical Association Inc

  16. Neutron Powder Diffraction in Sweden

    International Nuclear Information System (INIS)

    Tellgren, R.

    1986-01-01

    Neutron powder diffraction in Sweden has developed around the research reactor R2 in Studsvik. The article describes this facility and presents a historical review of research results obtained. It also gives some ideas of plans for future development

  17. Phonons from neutron powder diffraction

    Science.gov (United States)

    Dimitrov, D. A.; Louca, D.; Röder, H.

    1999-09-01

    The spherically averaged structure function S(\\|q\\|) obtained from pulsed neutron powder diffraction contains both elastic and inelastic scattering via an integral over energy. The Fourier transformation of S(\\|q\\|) to real space, as is done in the pair density function (PDF) analysis, regularizes the data, i.e., it accentuates the diffuse scattering. We present a technique which enables the extraction of off-center (\\|q\\|≠0) phonon information from powder diffraction experiments by comparing the experimental PDF with theoretical calculations based on standard interatomic potentials and the crystal symmetry. This procedure [dynamics from powder diffraction] has been successfully implemented as demonstrated here for two systems, a simple metal fcc Ni and an ionic crystal CaF2. Although computationally intensive, this data analysis allows for a phonon based modeling of the PDF, and additionally provides off-center phonon information from neutron powder diffraction.

  18. Powder Diffraction in Zeolite Science

    Science.gov (United States)

    Burton, Allen W.

    This tutorial discusses the fundamental principles of X-ray diffraction and its applications in zeolite science. The early sections review the physics of diffraction, crystal symmetry, and reciprocal space. We discuss how the intensity of diffracted radiation is affected both by geometric effects involving detection (the Lorentz-polarization factor) and by the arrangement of atoms within the crystal (the structure factor). The differences between powder diffraction and single-crystal diffraction are then described, and differences between X-ray and neutron diffraction are also discussed. Later sections describe the effects of symmetry, lattice substitution, crystallite size, residual strain, preferred orientation, and X-ray absorption. Special emphasis is placed on the proper application of the Scherrer analysis in reporting crystalize size. The principles of structure solution from direct methods and Patterson methods are then introduced, and a description of Rietveld analysis is given. Finally the effects of stacking disorder on a powder diffraction pattern are presented.

  19. Powder crystallography of useful materials using synchrotron radiation

    International Nuclear Information System (INIS)

    Kaduk, J.A.; Faber, J.; Pei, S.

    1994-01-01

    Synchrotron powder diffraction can, alone or in combination with other techniques, be used to answer real crystallographic questions. The high resolution and signal/background facilitate the ab initio solution of moderately-complex crystal structures from powder data, as illustrated by acentric structure of hydrated sodium aluminate, NaAlO 2 ·5/4H 2 O. Multiple-wavelength and resonant scattering studies can yield information not merely on the average crystal structure, but on local distortions from the average (the hydrogenation catalyst Cu 2 Al 6 B 4 O 17 ). Synchrotron radiation can place stringent requirements on the sample, as illustrated by studies of optical materials having the BaY 2 F 8 structure. Synchrotron powder diffraction studies of molecular sieve catalysts have proved useful in characterizing the framework composition (titanium MFI), extra framework species (cations and extra framework Al in FAU), and in characterizing crystallite size and strain. The authors have also applied synchrotron powder diffraction to the structural characterization of organic and coordination compounds

  20. Solving Crystal Structures from Powder Diffraction Data

    DEFF Research Database (Denmark)

    Christensen, A. Nørlund; Lehmann, M. S.; Nielsen, Mogens

    1985-01-01

    High resolution powder data from both neutron and X-ray (synchrotron) sources have been used to estimate the possibility of direct structure determination from powder data. Two known structures were resolved by direct methods with neutron and X-ray data. With synchrotron X-ray data, the measured ...

  1. The refractive-index correction in powder diffraction

    International Nuclear Information System (INIS)

    Hart, M.; Parrish, W.; Bellotto, M.; Lim, G.S.

    1988-01-01

    Throughout the history of powder diffraction practice there has been uncertainty about whether or not a refractive-index correction should be made to Bragg's law. High-precision Bragg-angle measurements have been performed with synchrotron radiation on SRM-640 silicon powders at glancing angles; it is found that little or no correction is necessary for the usual 2θ angle range. (orig.)

  2. Polycapillary optics for powder diffraction

    Science.gov (United States)

    Huang, Huapeng; MacDonald, Carolyn A.; Gibson, Walter M.; Chik, John; Parsegian, Adrian; Ponomarev, Igor Y.

    2001-12-01

    In this paper, we describe a low power system using Polycapillary collimating and focusing optics that were designed to collect Cu Ka radiation from an Oxford Ultra-Bright micro-focus source for X-ray powder diffraction measurements. The characterizations of the source and polycapillary optics are presented. A collimator with two apertures was used to block high energy X-rays. An optic alignment system was designed to optimize coupling between the optics and the source, taking into account the maximum radiation direction from the source. Several powder sample data sets were collected with this system and their qualities are compared with data sets from the same samples taken with an Enraf-Nonius FR590 sealed-tube source system. Discussion is also presented for further improving the performance of this low power system.

  3. Glancing angle synchrotron X-ray diffraction

    International Nuclear Information System (INIS)

    Cernik, R.J.

    1996-01-01

    This paper describes in basic detail some of the techniques that can be used to study thin films and surfaces. These are all in the X-ray region and cover reflectivity, diffraction form polycrystalline films, textured films and single crystal films. Other effects such as fluorescence and diffuse scattering are mentioned but not discussed in detail. Two examples of the reflectivity from multilayers and the diffraction from iron oxide films are discussed. The advantages of the synchrotron for these studies is stressed and the experimental geometries that can be employed are described i detail. A brief bibliography is provided at the end to accompany this part of the 1996 Frascati school

  4. Glancing angle synchrotron X-ray diffraction

    Energy Technology Data Exchange (ETDEWEB)

    Cernik, R.J. [Daresbury Lab., Warrington, WA (United States)

    1996-09-01

    This paper describes in basic detail some of the techniques that can be used to study thin films and surfaces. These are all in the X-ray region and cover reflectivity, diffraction form polycrystalline films, textured films and single crystal films. Other effects such as fluorescence and diffuse scattering are mentioned but not discussed in detail. Two examples of the reflectivity from multilayers and the diffraction from iron oxide films are discussed. The advantages of the synchrotron for these studies is stressed and the experimental geometries that can be employed are described i detail. A brief bibliography is provided at the end to accompany this part of the 1996 Frascati school.

  5. Development of materials science by Ab initio powder diffraction analysis

    International Nuclear Information System (INIS)

    Fujii, Kotaro

    2015-01-01

    Crystal structure is most important information to understand properties and behavior of target materials. Technique to analyze unknown crystal structures from powder diffraction data (ab initio powder diffraction analysis) enables us to reveal crystal structures of target materials even we cannot obtain a single crystal. In the present article, three examples are introduced to show the power of this technique in the field of materials sciences. The first example is dehydration/hydration of the pharmaceutically relevant material erythrocycin A. In this example, crystal structures of two anhydrous phases were determined from synchrotron X-ray powder diffraction data and their different dehydration/hydration properties were understood from the crystal structures. In the second example, a crystal structure of a three dimensional metal-organic-framework prepared by a mechanochemical reaction was determined from laboratory X-ray powder diffraction data and the reaction scheme has been revealed. In the third example, a crystal structure of a novel oxide-ion conductor of a new structure family was determined from synchrotron X-ray and neutron powder diffraction data which gave an important information to understand the mechanism of the oxide-ion conduction. (author)

  6. Powder diffraction crystallography of molecular solids.

    Science.gov (United States)

    Harris, Kenneth D M

    2012-01-01

    Many important crystalline solids cannot be prepared as single crystals of suitable size and quality for structural characterization by conventional single-crystal X-ray diffraction techniques and can instead be prepared only as microcrystalline powders. However, recent advances in techniques for determining crystal structures directly from powder X-ray diffraction data have created a unique opportunity for establishing structural properties of such materials. This chapter surveys the applications of powder X-ray diffraction across various aspects of structural and materials chemistry, focusing mainly on the opportunities that have emerged in recent years for carrying out complete crystal structure determination from powder X-ray diffraction data and giving particular emphasis to the case of molecular crystal structures. The current scope and future potential of powder X-ray diffraction as a strategy for crystal structure determination are discussed, and examples of applications across several disciplines of materials chemistry are presented.

  7. Structure resolution of Ba5Al3F19 and Iivestigation of fluorine ion dynamics by synchrotron powder diffraction, variable-temperature solid-state NMR, and quantum computations

    International Nuclear Information System (INIS)

    Martineau, C.; Fayon, F.; Suchomel, M.R.; Allix, M.; Massiot, D.; Taulelle, F.

    2011-01-01

    The room temperature structure of Ba 5 Al 3 F 19 has been solved using electron microscopy and synchrotron powder diffraction data. One-dimensional (1D) 27 Al and ultrafast magic-angle-spinning (MAS) 19 F NMR spectra have been recorded and are in agreement with the proposed structural model for Ba 5 Al 3 F 19 . The 19 F isotropic chemical shift and 27 Al quadrupolar parameters have been calculated using the CASTEP code from the experimental and density functional theory geometry-optimized structures. After optimization, the calculated NMR parameters of both the 19 F and 27 Al nuclei show improved consistency with the experimental values, demonstrating that the geometry optimization step is necessary to obtain more accurate and reliable structural data. This also enables a complete and unambiguous assignment of the 19 F MAS NMR spectrum of Ba 5 Al 3 F 19 . Variable-temperature 1D MAS 19 F NMR experiments have been carried out, showing the occurrence of fluorine ion mobility. Complementary insights were obtained from both two-dimensional (2D) exchange and 2D double-quantum dipolar recoupling NMR experiments, and a detailed analysis of the anionic motion in Ba 5 Al 3 F 19 is proposed, including the distinction between reorientational processes and chemical exchange involving bond breaking and re-formation.

  8. Possibilities of advanced powder diffraction utilizing J-PARC and SPring-8

    International Nuclear Information System (INIS)

    Sakata, Makoto; Nishibori, Eiji; Aoyagi, Shinobu; Hara, Yohei; Ohno, Atsuko

    2008-01-01

    The capability of powder diffraction has greatly increased in X-ray diffraction field since the advent of synchrotron light source, particularly third generation synchrotron source, such as SPring-8. In neutron field, J-PARC is about to start. This means we will have advanced powder diffraction instruments in both X-ray and neutron diffraction fields. The capability of powder diffraction is surely affected by the method used in data analysis. The most common analytical method is Rietveld refinement. Recently, the sophisticated analytical method called MEM/Rietveld, become powerful tool to extract the structural information included in the accurately measured experimental data. In this article, possibilities of powder diffraction utilizing advanced neutron source, i.e. J-PARC and/or advanced neutron and X-ray sources simultaneously, will be described bearing in mind that improvement of the advanced analytical method would occur. (author)

  9. In situ synchrotron X-ray powder diffraction study of the early hydration of α-tricalcium phosphate/tricalcium silicate composite bone cement

    Energy Technology Data Exchange (ETDEWEB)

    Morejon-Alonso, Loreley; Correa, Jose Raul, E-mail: lmorejon@fq.uh.cu [Departamento de Quimica General, Facultad de Quimica, Universidad de La Habana, UH (Cuba); Motisuke, Mariana [Universidade Federal de Sao Paulo (UNIFESP), Sao Jose dos Campos, SP (Brazil); Carrodeguas, Raul Garcia [Universidade Federal de Campina Grande (UFCG), Campina Grande, PB (Brazil). Laboratorio de Avaliacao e Desenvolvimento de Biomateriais do Nordeste; Santos, Luis Alberto dos [Universidade Federal do Rio Grande do Sul (UFRGS), Porto Alegre, RS (Brazil). Escola de Engenharia. Departamento de Materiais

    2015-01-15

    Bioactivity, osteogenicity and mechanical properties of α-tricalcium phosphate (α-TCP) based phosphates cements can be improved by adding tricalcium silicate (C{sub 3}S); however, the addition of C{sub 3}S delays the precipitation and growth of calcium deficient hydroxyapatite (CDHA). Thus, the aim of this work was the study of in situ setting reaction of α-TCP/C{sub 3}S composite bone cement under high energy X-ray generated by a synchrotron source within the first 72h. The results showed that the addition of C{sub 3}S induces the precipitation of nanosized CDHA at early times depending on the added content. Calculated crystallite sizes showed that the higher the content of C{sub 3}S, the smaller the crystal size at the beginning of the precipitation. These results are different from those obtained by conventional XRD method, suggesting that the proposed technique is a powerful tool in determining the composition and extent of reaction of CPCs surfaces in real time. (author)

  10. Comparison between powder and slices diffraction methods in teeth samples

    Energy Technology Data Exchange (ETDEWEB)

    Colaco, Marcos V.; Barroso, Regina C. [Universidade do Estado do Rio de Janeiro (IF/UERJ), RJ (Brazil). Inst. de Fisica. Dept. de Fisica Aplicada; Porto, Isabel M. [Universidade Estadual de Campinas (FOP/UNICAMP), Piracicaba, SP (Brazil). Fac. de Odontologia. Dept. de Morfologia; Gerlach, Raquel F. [Universidade de Sao Paulo (FORP/USP), Rieirao Preto, SP (Brazil). Fac. de Odontologia. Dept. de Morfologia, Estomatologia e Fisiologia; Costa, Fanny N. [Coordenacao dos Programas de Pos-Graduacao de Engenharia (LIN/COPPE/UFRJ), RJ (Brazil). Lab. de Instrumentacao Nuclear

    2011-07-01

    Propose different methods to obtain crystallographic information about biological materials are important since powder method is a nondestructive method. Slices are an approximation of what would be an in vivo analysis. Effects of samples preparation cause differences in scattering profiles compared with powder method. The main inorganic component of bones and teeth is a calcium phosphate mineral whose structure closely resembles hydroxyapatite (HAp). The hexagonal symmetry, however, seems to work well with the powder diffraction data, and the crystal structure of HAp is usually described in space group P63/m. Were analyzed ten third molar teeth. Five teeth were separated in enamel, detin and circumpulpal detin powder and five in slices. All the scattering profile measurements were carried out at the X-ray diffraction beamline (XRD1) at the National Synchrotron Light Laboratory - LNLS, Campinas, Brazil. The LNLS synchrotron light source is composed of a 1.37 GeV electron storage ring, delivering approximately 4x10{sup -1}0 photons/s at 8 keV. A double-crystal Si(111) pre-monochromator, upstream of the beamline, was used to select a small energy bandwidth at 11 keV . Scattering signatures were obtained at intervals of 0.04 deg for angles from 24 deg to 52 deg. The human enamel experimental crystallite size obtained in this work were 30(3)nm (112 reflection) and 30(3)nm (300 reflection). These values were obtained from measurements of powdered enamel. When comparing the slice obtained 58(8)nm (112 reflection) and 37(7)nm (300 reflection) enamel diffraction patterns with those generated by the powder specimens, a few differences emerge. This work shows differences between powder and slices methods, separating characteristics of sample of the method's influence. (author)

  11. Comparison between powder and slices diffraction methods in teeth samples

    International Nuclear Information System (INIS)

    Colaco, Marcos V.; Barroso, Regina C.; Porto, Isabel M.; Gerlach, Raquel F.; Costa, Fanny N.

    2011-01-01

    Propose different methods to obtain crystallographic information about biological materials are important since powder method is a nondestructive method. Slices are an approximation of what would be an in vivo analysis. Effects of samples preparation cause differences in scattering profiles compared with powder method. The main inorganic component of bones and teeth is a calcium phosphate mineral whose structure closely resembles hydroxyapatite (HAp). The hexagonal symmetry, however, seems to work well with the powder diffraction data, and the crystal structure of HAp is usually described in space group P63/m. Were analyzed ten third molar teeth. Five teeth were separated in enamel, detin and circumpulpal detin powder and five in slices. All the scattering profile measurements were carried out at the X-ray diffraction beamline (XRD1) at the National Synchrotron Light Laboratory - LNLS, Campinas, Brazil. The LNLS synchrotron light source is composed of a 1.37 GeV electron storage ring, delivering approximately 4x10 -1 0 photons/s at 8 keV. A double-crystal Si(111) pre-monochromator, upstream of the beamline, was used to select a small energy bandwidth at 11 keV . Scattering signatures were obtained at intervals of 0.04 deg for angles from 24 deg to 52 deg. The human enamel experimental crystallite size obtained in this work were 30(3)nm (112 reflection) and 30(3)nm (300 reflection). These values were obtained from measurements of powdered enamel. When comparing the slice obtained 58(8)nm (112 reflection) and 37(7)nm (300 reflection) enamel diffraction patterns with those generated by the powder specimens, a few differences emerge. This work shows differences between powder and slices methods, separating characteristics of sample of the method's influence. (author)

  12. High-pressure phases of uranium monophosphide studied by synchrotron x-ray diffraction

    DEFF Research Database (Denmark)

    Olsen, J. Staun; Gerward, Leif; Benedict, U.

    1988-01-01

    X-ray diffraction studies have been performed on UP powder for pressures up to 51 GPa using synchrotron radiation and a diamond-anvil cell. At ambient pressure UP has the rocksalt structure. The bulk modulus has been determined to B0=102(4) GPa and its pressure derivative to B0’=4.0(8). The cubic...

  13. Energy-dispersive X-ray diffraction beamline at Indus-2 synchrotron ...

    Indian Academy of Sciences (India)

    The first two parameters are discussed in the optical design part of ... 2.1.1 Optical design. Low divergence of incident beam is one of the basic character- istics of synchrotron radiation. It is known to vary as 1/γ where γ = (m/m0) = 1/ .... diffraction data of the powdered LaB6 sample were recorded under ambient conditions.

  14. Determination of organic crystal structures by X ray powder diffraction

    CERN Document Server

    McBride, L

    2000-01-01

    The crystal structure of Ibuprofen has been solved from synchrotron X-ray powder diffraction data using a genetic algorithm (GA). The performance of the GA is improved by incorporating prior chemical information in the form of hard limits on the values that can be taken by the flexible torsion angles within the molecule. Powder X-ray diffraction data were collected for the anti-convulsant compounds remacemide, remacemide nitrate and remacemide acetate at 130 K on BM 16 at the X-ray European Synchrotron Radiation Facility (ESRF) at Grenoble. High quality crystal structures were obtained using data collected to a resolution of typically 1.5 A. The structure determinations were performed using a simulated annealing (SA) method and constrained Rietveld refinements for the structures converged to chi sup 2 values of 1.64, 1.84 and 1.76 for the free base, nitrate and acetate respectively. The previously unknown crystal structure of the drug famotidine Form B has been solved using X-ray powder diffraction data colle...

  15. Nuclear dynamical diffraction using synchrotron radiation

    Energy Technology Data Exchange (ETDEWEB)

    Brown, Dennis Eugene [Stanford Univ., CA (United States)

    1993-05-01

    The scattering of synchrotron radiation by nuclei is extensively explored in this thesis. From the multipole electric field expansion resulting from time-dependent nonrelativistic perturbation theory, a dynamical scattering theory is constructed. This theory is shown, in the many particle limit, to be equivalent to the semi-classical approach where a quantum mechanical scattering amplitude is used in the Maxwell inhomogeneous wave equation. The Moessbauer specimen whose low-lying energy levels were probed is a ferromagnetic lattice of 57Fe embedded in a yttrium iron garnet (YIG) crystal matrix. The hyperfine fields in YIG thin films were studied at low and room temperature using time-resolved quantum beat spectroscopy. Nuclear hyperfine structure quantum beats were measured using a fast plastic scintillator coincidence photodetector and associated electronics having a time resolution of 2.5 nsec. The variation of the quantum beat patterns near the Bragg [0 0 2] diffraction peak gave a Lamb-Moessbauer factor of 8.2±0.4. Exploring characteristic dynamical features in the higher order YIG [0 0 10] reflection revealed that one of the YIG crystals had bifurcated into two different layers. The dynamics of nuclear superradiance was explored. This phenomenon includes the radiative speedup exhibited by a collective state of particles, and, in striking concurrence, resonance frequency shifts. A speedup of a factor of 4 in the total decay rate and a beat frequency shift of 11/2 natural resonance linewidths were observed. Nuclear resonance scattering was also found to be a useful way of performing angular interferometry experiments, and it was used to observe the phase shift of a rotated quantum state. On the whole, nuclear dynamical diffraction theory has superbly explained many of the fascinating features of resonant magnetic dipole radiation scattered by a lattice of nuclei.

  16. Nuclear dynamical diffraction using synchrotron radiation

    International Nuclear Information System (INIS)

    Brown, D.E.

    1993-05-01

    The scattering of synchrotron radiation by nuclei is extensively explored in this thesis. From the multipole electric field expansion resulting from time-dependent nonrelativistic perturbation theory, a dynamical scattering theory is constructed. This theory is shown, in the many particle limit, to be equivalent to the semi-classical approach where a quantum mechanical scattering amplitude is used in the Maxwell inhomogeneous wave equation. The Moessbauer specimen whose low-lying energy levels were probed is a ferromagnetic lattice of 57 Fe embedded in a yttrium iron garnet (YIG) crystal matrix. The hyperfine fields in YIG thin films were studied at low and room temperature using time-resolved quantum beat spectroscopy. Nuclear hyperfine structure quantum beats were measured using a fast plastic scintillator coincidence photodetector and associated electronics having a time resolution of 2.5 nsec. The variation of the quantum beat patterns near the Bragg [0 0 2] diffraction peak gave a Lamb-Moessbauer factor of 8.2±0.4. Exploring characteristic dynamical features in the higher order YIG [0 0 10] reflection revealed that one of the YIG crystals had bifurcated into two different layers. The dynamics of nuclear superradiance was explored. This phenomenon includes the radiative speedup exhibited by a collective state of particles, and, in striking concurrence, resonance frequency shifts. A speedup of a factor of 4 in the total decay rate and a beat frequency shift of 1 1/2 natural resonance linewidths were observed. Nuclear resonance scattering was also found to be a useful way of performing angular interferometry experiments, and it was used to observe the phase shift of a rotated quantum state. On the whole, nuclear dynamical diffraction theory has superbly explained many of the fascinating features of resonant magnetic dipole radiation scattered by a lattice of nuclei

  17. An introduction to neutron powder diffraction

    International Nuclear Information System (INIS)

    Kennedy, S.

    1999-01-01

    Full text: The aim of this presentation is to provide an introduction to neutron powder diffraction. The technique has developed from humble beginnings in the first generation of nuclear reactors in the late 1940's, to become one of the most widely used and productive forms of neutron beam research. Its popularity stems from the unique properties of thermal neutrons, which make them the ideal probe for obtaining spatial and dynamic information about atomic nuclei and magnetic dipoles in condensed matter. Neutron powder diffraction is particularly useful for location of lighter elements, in magnetic structure determination, for understanding thermal motions of atoms and for in-situ studies of materials at extreme temperatures and pressures. It is commonly used for research in condensed matter physics, structural chemistry and materials science at nuclear research reactors and spallation neutron sources around the world. The basic properties of thermal neutrons that are exploited in condensed matter research will be described. The neutron powder diffraction technique will be discussed with particular attention to comparisons with the X-ray powder diffraction technique, to which it is complementary. A brief description of the neutron powder diffraction facilities at ANSTO's HIFAR research reactor will be given, along with selected examples of neutron diffraction experiments that illustrate the power of the technique. Copyright (1999) Australian X-ray Analytical Association Inc

  18. Structure determination from powder diffraction data.

    Science.gov (United States)

    David, W I F; Shankland, K

    2008-01-01

    Advances made over the past decade in structure determination from powder diffraction data are reviewed with particular emphasis on algorithmic developments and the successes and limitations of the technique. While global optimization methods have been successful in the solution of molecular crystal structures, new methods are required to make the solution of inorganic crystal structures more routine. The use of complementary techniques such as NMR to assist structure solution is discussed and the potential for the combined use of X-ray and neutron diffraction data for structure verification is explored. Structures that have proved difficult to solve from powder diffraction data are reviewed and the limitations of structure determination from powder diffraction data are discussed. Furthermore, the prospects of solving small protein crystal structures over the next decade are assessed.

  19. Uniting Electron Crystallography and Powder Diffraction

    CERN Document Server

    Shankland, Kenneth; Meshi, Louisa; Avilov, Anatoly; David, William

    2012-01-01

    The polycrystalline and nanocrystalline states play an increasingly important role in exploiting the properties of materials, encompassing applications as diverse as pharmaceuticals, catalysts, solar cells and energy storage. A knowledge of the three-dimensional atomic and molecular structure of materials is essential for understanding and controlling their properties, yet traditional single-crystal X-ray diffraction methods lose their power when only polycrystalline and nanocrystalline samples are available. It is here that powder diffraction and single-crystal electron diffraction techniques take over, substantially extending the range of applicability of the crystallographic principles of structure determination.  This volume, a collection of teaching contributions presented at the Crystallographic Course in Erice in 2011, clearly describes the fundamentals and the state-of-the-art of powder diffraction and electron diffraction methods in materials characterisation, encompassing a diverse range of discipl...

  20. Advances in powder diffraction crystallography

    International Nuclear Information System (INIS)

    Magneli, A.

    1986-01-01

    This is the first conference to be arranged within the framework of an agreement on scientific exchange and co-operation between l Academie des Sciences de l Institut de France and the Royal Swedish Academy of Sciences. The responsibility for the scientific program of the conference has been shared between members of the two Academies. The contributions include glimpses of the historical background and broad reviews of the present status of development and of recent work in powder crystallography. Reports are given on a number of studies, basic as well as applied in character, currently conducted in the two countries in a large variety of fields. Prospects of further developments in the area are also presented

  1. Structures of mono-unsaturated triacylglycerols. V. The β'1-2, β'-3 and β2-3 polymorphs of 1,3-dilauroyl-2-oleoylglycerol (LaOLa) from synchrotron and laboratory powder diffraction data

    NARCIS (Netherlands)

    van Mechelen, J.B.; Goubitz, K.; Pop, M.; Peschar, R.; Schenk, H.

    2008-01-01

    The crystal structures of the β'1-2, the β'-3 and the β2-3 polymorphs of 1,3-dilauroyl-2-oleoylglycerol have been solved from powder diffraction data. The packing of the β2-3 polymorph is similar to that of other cis mono-unsaturated triacylglycerols. Both the β' polymorphs are crystallized in a

  2. Neutron Powder Diffraction and Constrained Refinement

    DEFF Research Database (Denmark)

    Pawley, G. S.; Mackenzie, Gordon A.; Dietrich, O. W.

    1977-01-01

    The first use of a new program, EDINP, is reported. This program allows the constrained refinement of molecules in a crystal structure with neutron diffraction powder data. The structures of p-C6F4Br2 and p-C6F4I2 are determined by packing considerations and then refined with EDINP. Refinement...

  3. Time-resolved Neutron Powder Diffraction

    International Nuclear Information System (INIS)

    Pannetier, J.

    1986-01-01

    The use of a high-flux neutron source together with a large position sensitive detector (PSD) allows a powder diffraction pattern to be recorded at a time-scale of a few minutes so that crystalline systems under non-equilibrium conditions may now conveniently be investigated. This introduces a new dimension into powder diffraction (the time and transient phenomena like heterogeneous chemical reactions can now be easily studied. The instrumental parameters relevant for the design of such time-dependent experiments are briefly surveyed and the current limits of the method are discussed. The applications are illustrated by two kinds of experiment in the field of inorganic solid state chemistry: true kinetic studies of heterogeneous chemical reactions and thermodiffractometry experiments

  4. Powder Neutron Diffraction and Magnetic structures

    International Nuclear Information System (INIS)

    Vigneron, F.

    1986-01-01

    The determination of the magnetic structures of materials (ferromagnetic, antiferromagnetic, helimagnetic, .) can be achieved only by neutron diffraction. A general survey of the powder technique is given: 2-axis spectrometer and analysis of the magnetic data. For the REBe/sb13/ intermetallic compounds (RE = Rare Earth), commensurate and/or incommensurate magnetic structures are observed and discussed as a function of RE (Gd, Tb, Dy, Ho, Er)

  5. Neutron powder diffraction and high Tc superconductors

    International Nuclear Information System (INIS)

    Hewat, A.W.

    1988-01-01

    Neutron powder diffraction is a technique for determining the crystalline structure and texture of materials for which single crystals cannot be obtained. As such it has made important contributions to the characterisation and understanding of the new high temperature superconductors. As well, NPD has wide applications in materials science, ranging from the study of catalyst and zeolite structures, to the texture of railway lines and composite superconducting wires. (orig.)

  6. X-ray diffraction microtomography using synchrotron radiation

    CERN Document Server

    Barroso, R C; Jesus, E F O; Oliveira, L F

    2001-01-01

    The X-ray diffraction computed tomography technique is based on the interference phenomena of the coherent scatter. For low-momentum transfer, it is most probable that the scattering interaction will be coherent. A selective discrimination of a given element in a scanned specimen can be realized by fixing the Bragg angle which produces an interference peak and then, to carry out the computed tomography in the standard mode. The image reconstructed exalts the presence of this element with respect to other ones in a sample. This work reports the feasibility of a non-destructive synchrotron radiation X-ray diffraction imaging technique. This research was performed at the X-ray Diffraction beam line of the National Synchrotron Light Laboratory (LNLS) in Brazil. The coherent scattering properties of different tissue and bone substitute materials were evaluated. Furthermore, diffraction patterns of some polycrystalline solids were studied due to industrial and environmental human exposure to these metals. The obtai...

  7. Neutron powder diffraction study of methane hydrate

    International Nuclear Information System (INIS)

    Ishii, Yoshinobu

    2005-01-01

    Neutron powder diffraction study of methane hydrate has been conducted in the temperature range of 7 K to 185 K. The diffraction data were analyzed by the Rietveld refinement and the Maximum Entropy Method (MEM). From MEM analysis, we obtained the scattering-length density distributions in a 3-dimensional image. The scattering-length density corresponding to C atom of the methane molecule was appeared and no density of H atoms was found in the small cage over the measured temperature range. On the other hand, in the large cage the scattering-length densities related to both H atom and C atom were observed at low temperature. The scattering-length density of H atom disappeared with increasing temperature, and then the scattering-length density of methane was almost gone at high temperature. These results show the motion of methane molecules differ in the small cage as compared to the large cage

  8. Neutron powder diffraction study on fully hydrogenated amino acid molecules

    International Nuclear Information System (INIS)

    Jiao Xuesheng; Sun Kai; Han Wenze; Liu Yuntao; Chen Dongfeng

    2010-01-01

    The traditional methods for studying amino acid molecular structure are X-ray diffraction and neutron diffraction after deuteration. In this paper, X-ray diffraction, neutron powder diffraction and Raman scattering were used to study the molecular structure of alanine and leucine. Combination of infrared spectroscopy, compared with fully hydrogenated, partial deuterated and fully deuterated alanine molecules, it is shown that the traditional methods are not enough in the study of molecular structure. Meanwhile, the neutron powder diffraction method was used to measure the leucine molecule directly. It shows that neutron powder diffraction method can give the fine structure of leucine molecule. (authors)

  9. Synchrotron diffraction characterization of nanostructured KY3F10:Tb

    International Nuclear Information System (INIS)

    Ichikawa, Rodrigo U.; Teixeira, Maria I.; Ranieri, Izilda M.; Martinez, Luis G.; Linhares, Horacio M.S.M.D.; Turrillas, Xavier

    2015-01-01

    Nanostructured rare-earth fluorides materials are being intensively studied recently due to their potential applications in high-dose dosimetry. Particularly, nanostructured Tb-doped KY 3 F 10 has shown satisfactory results to be used in this area. In the present work, the structure and microstructure of KY 3 F 10 :Tb was investigated by means of X-ray synchrotron diffraction. One of the samples was analyzed as synthesized and another after a heat treatment. Rietveld refinement of synchrotron diffraction data was applied to obtain cell parameters, atomic positions and atomic displacement factors and the results were compared to values found in literature. X-ray line profile analysis methods were applied to determine mean crystallite sizes and their distribution. (author)

  10. Beamline I11 at Diamond: a new instrument for high resolution powder diffraction.

    Science.gov (United States)

    Thompson, S P; Parker, J E; Potter, J; Hill, T P; Birt, A; Cobb, T M; Yuan, F; Tang, C C

    2009-07-01

    The performance characteristics of a new synchrotron x-ray powder diffraction beamline (I11) at the Diamond Light Source are presented. Using an in-vacuum undulator for photon production and deploying simple x-ray optics centered around a double-crystal monochromator and a pair of harmonic rejection mirrors, a high brightness and low bandpass x-ray beam is delivered at the sample. To provide fast data collection, 45 Si(111) analyzing crystals and detectors are installed onto a large and high precision diffractometer. High resolution powder diffraction data from standard reference materials of Si, alpha-quartz, and LaB6 are used to characterize instrumental performance.

  11. Powder diffraction studies using anomalous dispersion

    International Nuclear Information System (INIS)

    Cox, D.E.; Wilkinson, A.P.

    1993-01-01

    With the increasing availability and accessibility of high resolution powder diffractometers at many synchrotron radiation sources throughout the world, there is rapidly-growing interest in the exploitation of anomalous dispersion techniques for structural studies of polycrystalline materials. In conjunction with the Rietveld profile method for structure refinement, such studies are especially useful for the determination of the site distributions of two or more atoms which are near neighbors in the periodic table, or atoms which are distributed among partially occupied sites. Additionally, it is possible to (1) determine the mean-square displacements associated with different kinds of atoms distributed over a single set of sites, (2) distinguish between different oxidation states and coordination geometries of a particular atom in a compound and (3) to determine f' for a wide range of atomic species as a function of energy in the vicinity of an absorption edge. Experimental methods for making anomalous dispersion measurements are described in some detail, including data collection strategies, data analysis and correlation problems, possible systematic errors, and the accuracy of the results. Recent work in the field is reviewed, including cation site-distribution studies (e.g. doped high T c superconductors, ternary alloys, FeCo 2 (PO 4 ) 3 , FeNi 2 BO 5 ), oxidation-state contrast (e.g. YBa 2 Cu 3 O 6+x , Eu 3 O 4 , GaCl 2 , Fe 2 PO 5 ), and the effect of coordination geometry (e.g. Y 3 Ga 5 O l2 )

  12. Pulsed Neutron Powder Diffraction for Materials Science

    Science.gov (United States)

    Kamiyama, T.

    2008-03-01

    The accelerator-based neutron diffraction began in the end of 60's at Tohoku University which was succeeded by the four spallation neutron facilities with proton accelerators at the High Energy Accelerator Research Organization (Japan), Argonne National Laboratory and Los Alamos Laboratory (USA), and Rutherford Appleton Laboratory (UK). Since then, the next generation source has been pursued for 20 years, and 1MW-class spallation neutron sources will be appeared in about three years at the three parts of the world: Japan, UK and USA. The joint proton accelerator project (J-PARC), a collaborative project between KEK and JAEA, is one of them. The aim of the talk is to describe about J-PARC and the neutron diffractometers being installed at the materials and life science facility of J-PARC. The materials and life science facility of J-PARC has 23 neutron beam ports and will start delivering the first neutron beam of 25 Hz from 2008 May. Until now, more than 20 proposals have been reviewed by the review committee, and accepted proposal groups have started to get fund. Those proposals include five polycrystalline diffractometers: a super high resolution powder diffractometer (SHRPD), a 0.2%-resolution powder diffractometer of Ibaraki prefecture (IPD), an engineering diffractometers (Takumi), a high intensity S(Q) diffractometer (VSD), and a high-pressure dedicated diffractometer. SHRPD, Takumi and IPD are being designed and constructed by the joint team of KEK, JAEA and Ibaraki University, whose member are originally from the KEK powder group. These three instruments are expected to start in 2008. VSD is a super high intensity diffractometer with the highest resolution of Δd/d = 0.3%. VSD can measure rapid time-dependent phenomena of crystalline materials as well as glass, liquid and amorphous materials. The pair distribution function will be routinely obtained by the Fourier transiformation of S(Q) data. Q range of VSD will be as wide as 0.01 Å-1Software group is

  13. Development and directions of powder diffraction on proteins

    International Nuclear Information System (INIS)

    Von Dreele, R.B.; Besnard, C.; Basso, S.; Camus, F.; Pattison, P.; Schiltz, M.; Wright, J.P.; Margiolaki, R.; Fitch, A.N.; Fox, G.C.; Prugoveeki, S.; Beckers, D.; Helliwell, J.R.; Helliwell, M.; Jones, R.H.; Roberts, M.A.; Miura, K.; Kahn, R.; Giacovazzo, C.; Altomare, A.; Caliandro, R.; Camalli, M.; Cuocci, C.; Moliterni, A.G.G.; Rizzi, R.; Hinrichsen, B.; Kern, A.; Coelho, A.A.; Degen, T.; Kokkinidis, M.; Fadouloglou, V.; Gazi, A.; Panopoulos, N.; Pinotsis, N.; Wilmanns, M.; Norrman, M.; Schluckebier, G.; Prugoveeki, B.; Dilovic, J.; Matkovic-Calogovic, D.; Bill, David; Markvardsen, A.; Grosse-Kunstleve, R.; Rius, J.; Glykos Nicholas, M.; Murshudov, G.N.

    2007-01-01

    X-ray diffraction is one of the most important method for obtaining information about the structure of proteins and thereby for gaining insight into fundamental biological and biochemical mechanisms. This seminar was dedicated to X-ray powder diffraction and was organized around 6 sessions: 1) what can powder diffraction do for proteins?, 2) adapting experimentally to proteins, 3) interpreting powder data, 4) the world of protein crystallography, 5) advancing methods for powder data analysis, and 6) transferable methods from single crystals. This document gathers the abstracts of the 23 papers presented. (A.C.)

  14. Development and directions of powder diffraction on proteins

    Energy Technology Data Exchange (ETDEWEB)

    Von Dreele, R.B.; Besnard, C.; Basso, S.; Camus, F.; Pattison, P.; Schiltz, M.; Wright, J.P.; Margiolaki, R.; Fitch, A.N.; Fox, G.C.; Prugoveeki, S.; Beckers, D.; Helliwell, J.R.; Helliwell, M.; Jones, R.H.; Roberts, M.A.; Miura, K.; Kahn, R.; Giacovazzo, C.; Altomare, A.; Caliandro, R.; Camalli, M.; Cuocci, C.; Moliterni, A.G.G.; Rizzi, R.; Hinrichsen, B.; Kern, A.; Coelho, A.A.; Degen, T.; Kokkinidis, M.; Fadouloglou, V.; Gazi, A.; Panopoulos, N.; Pinotsis, N.; Wilmanns, M.; Norrman, M.; Schluckebier, G.; Prugoveeki, B.; Dilovic, J.; Matkovic-Calogovic, D.; Bill, David; Markvardsen, A.; Grosse-Kunstleve, R.; Rius, J.; Glykos Nicholas, M.; Murshudov, G.N

    2007-07-01

    X-ray diffraction is one of the most important method for obtaining information about the structure of proteins and thereby for gaining insight into fundamental biological and biochemical mechanisms. This seminar was dedicated to X-ray powder diffraction and was organized around 6 sessions: 1) what can powder diffraction do for proteins?, 2) adapting experimentally to proteins, 3) interpreting powder data, 4) the world of protein crystallography, 5) advancing methods for powder data analysis, and 6) transferable methods from single crystals. This document gathers the abstracts of the 23 papers presented. (A.C.)

  15. Pulsed Neutron Powder Diffraction for Materials Science

    International Nuclear Information System (INIS)

    Kamiyama, T.

    2008-01-01

    The accelerator-based neutron diffraction began in the end of 60's at Tohoku University which was succeeded by the four spallation neutron facilities with proton accelerators at the High Energy Accelerator Research Organization (Japan), Argonne National Laboratory and Los Alamos Laboratory (USA), and Rutherford Appleton Laboratory (UK). Since then, the next generation source has been pursued for 20 years, and 1MW-class spallation neutron sources will be appeared in about three years at the three parts of the world: Japan, UK and USA. The joint proton accelerator project (J-PARC), a collaborative project between KEK and JAEA, is one of them. The aim of the talk is to describe about J-PARC and the neutron diffractometers being installed at the materials and life science facility of J-PARC. The materials and life science facility of J-PARC has 23 neutron beam ports and will start delivering the first neutron beam of 25 Hz from 2008 May. Until now, more than 20 proposals have been reviewed by the review committee, and accepted proposal groups have started to get fund. Those proposals include five polycrystalline diffractometers: a super high resolution powder diffractometer (SHRPD), a 0.2%-resolution powder diffractometer of Ibaraki prefecture (IPD), an engineering diffractometers (Takumi), a high intensity S(Q) diffractometer (VSD), and a high-pressure dedicated diffractometer. SHRPD, Takumi and IPD are being designed and constructed by the joint team of KEK, JAEA and Ibaraki University, whose member are originally from the KEK powder group. These three instruments are expected to start in 2008. VSD is a super high intensity diffractometer with the highest resolution of Δd/d = 0.3%. VSD can measure rapid time-dependent phenomena of crystalline materials as well as glass, liquid and amorphous materials. The pair distribution function will be routinely obtained by the Fourier transiformation of S(Q) data. Q range of VSD will be as wide as 0.01 A -1 -1 . IPD is fully

  16. Oxides neutron and synchrotron X-ray diffraction studies

    CERN Document Server

    Sosnowska, I M

    1999-01-01

    We review some results from several areas of oxide science in which neutron scattering and X-ray synchrotron scattering exercise a complementary role to high-resolution transmission electron microscopy. The very high-resolution time-of-flight neutron diffraction technique and its role in studies of the magnetic structure of oxides is especially reviewed. The selected topics of structural studies for the chosen oxides are: crystal and magnetic structure of the so-called cellular random systems, magnetic structure and phase transitions in ferrites and the behaviour of water in non-stoichiometric protonic conductors and in the opal silica-water system. (40 refs).

  17. Synchrotron X-ray diffraction using triple-axis spectrometry

    International Nuclear Information System (INIS)

    Als-Nielsen, J.

    1980-12-01

    High resolution X-ray diffraction studies of (i) monolayers of the noble gases Kr and Ar physiosorbed on graphite (ii) smectic A fluctuations in the nematic and the smectic A phases of liquid crystals are described. The apparatus used is a triple axis spectrometer situated at the storage ring DORIS at Hasylab, DESY, Hamburg. A monochromatic, well collimated beam is extracted from the synchrotron radiation spectrum by Bragg reflection from perfect Si or Ge crystals. The direction of the beam scattered from the sample is determined by Bragg reflection from a perfect Si or Ge crystal. High intensities even with resolution extending beyond the wavelength of visible light can be obtained. (Auth.)

  18. Structure determination of modulated structures by powder X-ray diffraction and electron diffraction

    Czech Academy of Sciences Publication Activity Database

    Zhou, Z.Y.; Palatinus, Lukáš; Sun, J.L.

    2016-01-01

    Roč. 3, č. 11 (2016), s. 1351-1362 ISSN 2052-1553 Institutional support: RVO:68378271 Keywords : electron diffraction * incommensurate structure * powder diffraction Subject RIV: BM - Solid Matter Physics ; Magnetism Impact factor: 4.036, year: 2016

  19. Analysis of synchrotron X-ray diffraction patterns from fluorotic enamel samples

    Energy Technology Data Exchange (ETDEWEB)

    Almeida, Ana P.G.; Braz, Delson, E-mail: anapaulagalmeida@gmail.co [Coordenacao dos Programas de Pos-graduacao de Engenharia (COPPE/UFRJ), Rio de Janeiro, RJ (Brazil). Lab. de Instrumentacao Nuclear; Colaco, Marcos V.; Barroso, Regina C., E-mail: cely@uerj.b [Universidade do Estado do Rio de Janeiro (UERJ), RJ (Brazil). Inst. de Fisica; Porto, Isabel M., E-mail: belporto@ig.com.b [Universidade Estadual de Campinas (UNICAMP), Piracicaba, SP (Brazil). Faculdade de Odontologia; Gerlach, Raquel F., E-mail: rfgerlach@forp.usp.b [Universidade de Sao Paulo (USP), Ribeirao Preto, SP (Brazil). Faculdade de Odontologia; Droppa Junior, Roosevelt, E-mail: rdroppa@lnls.b [Associacao Brasileira de Tecnologia de Luz Sincrotron (ABTLuS), Campinas, SP (Brazil)

    2009-07-01

    With the introduction of fluoride as the main anticaries agent used in preventive dentistry, and perhaps an increase in fluoride in our food chain, dental fluorosis has become an increasing world-wide problem. Visible signs of fluorosis begin to become obvious on the enamel surface as opacities, implying some porosity in the tissue. The mechanisms that conduct the formation of fluorotic enamel are unknown, but should involve modifications in the basics physical-chemistry reactions of demineralisation and remineralisation of the enamel of the teeth, which is the same reaction of formation of the enamel's hydroxyapatite (HAp) in the maturation phase. The increase of the amount of fluoride inside of the apatite will result in gradual increase of the lattice parameters. The hexagonal symmetry seems to work well with the powder diffraction data, and the crystal structure of HAp is usually described in space group P63/m. The aim of this work is to characterize the healthy and fluorotic enamel in human tooth using technique Synchrotron X-ray diffraction in order to determine the crystal structure and crystallinity of on fluoroapatite (FAp) crystal present in fluoritic enamel. All the scattering profile measurements was carried out at the X-ray diffraction beamline (XRD1) at the National Synchrotron Light Laboratory - LNLS, Campinas, Brazil. (author)

  20. Microelemental and mineral compositions of pathogenic biomineral concrements: SRXFA, X-ray powder diffraction and vibrational spectroscopy data

    Energy Technology Data Exchange (ETDEWEB)

    Moroz, T.N. [Institute of Geology and Mineralogy, SB RAS, Pr. Akad. Koptyuga, 3, 630090 Novosibirsk (Russian Federation)], E-mail: moroz@uiggm.nsc.ru; Palchik, N.A.; Dar' in, A.V. [Institute of Geology and Mineralogy, SB RAS, Pr. Akad. Koptyuga, 3, 630090 Novosibirsk (Russian Federation)

    2009-05-11

    X-ray fluorescence analysis using synchrotron radiation (SRXRF), X-ray powder diffraction, infrared and Raman spectroscopy had been applied for determination of microelemental and mineral composition of the kidney stones, gallstones and salivalities from natives of Novosibirsk and Novosibirsk region, Russia. The relationship between mineral, organic and microelemental composition of pathogenic calcilus was shown.

  1. Ab initio structure determination via powder X-ray diffraction

    Indian Academy of Sciences (India)

    Unknown

    Powder data is especially useful to deduce accurate cell parameters. Rietveld's refinement procedure1,2 has revolutionized the application of powder X-ray diffraction by resulting in a large number of structures being refined in the last decade. If a suitable starting model is available, it has become routine to refine structures ...

  2. Rietveld refinement of the orthorhombic Pbca structures of Rb2CdSi5O12, Cs2MnSiO5O12, Cs2CoSi5O12 and Cs2NiSi5O12 leucites by synchrotron X-ray powder diffraction

    International Nuclear Information System (INIS)

    Bell, A.M.T.; Henderson, C.M.B.

    1996-01-01

    Analysis of high-resolution synchrotron X-ray powder diffraction patterns for hydrothermally synthesized Rb 2 CdSi 5 O 12 and Cs 2 MnSi 5 O 12 leucite analogues, and dry-synthesized Cs 2 CoSi 5 O 12 and Cs 2 NiSi 5 O 12 leucite analogues showed that they have an orthorhombic Pbca structure. The structures have been refined by the Rietveld method, showing that the tetrahedrally coordinated atoms (Si, Cd, Mn, Co and Ni) are ordered on separate sites. The Cs 2 MnSi 5 O 12 , Cs 2 CoSi 5 O 12 and Cs 2 NiSi 5 O 12 leucite samples are unusual in containing SiO 4 tetrahedra which are more distorted, on average, than the larger MnO 4 , CoO 4 and NiO 4 tetrahedra. The JCPDS file numbers for Rb 2 CdSi 5 O 12 , Cs 2 MnSi 5 O 12 and Cs 2 CoSi 5 O 12 are 46-1491, 46-1492 and 46-1493, respectively. (orig.)

  3. Beamline I11 at Diamond: A new instrument for high resolution powder diffraction

    Energy Technology Data Exchange (ETDEWEB)

    Thompson, S. P.; Parker, J. E.; Potter, J.; Hill, T. P.; Birt, A.; Cobb, T. M.; Yuan, F.; Tang, C. C. [Diamond Light Source, Harwell Science and Innovation Campus, Didcot, Oxfordshire OX11 0DE (United Kingdom)

    2009-07-15

    The performance characteristics of a new synchrotron x-ray powder diffraction beamline (I11) at the Diamond Light Source are presented. Using an in-vacuum undulator for photon production and deploying simple x-ray optics centered around a double-crystal monochromator and a pair of harmonic rejection mirrors, a high brightness and low bandpass x-ray beam is delivered at the sample. To provide fast data collection, 45 Si(111) analyzing crystals and detectors are installed onto a large and high precision diffractometer. High resolution powder diffraction data from standard reference materials of Si, {alpha}-quartz, and LaB{sub 6} are used to characterize instrumental performance.

  4. Optimizing Monocapillary Optics for Synchrotron X-ray Diffraction, Fluorescence Imaging, and Spectroscopy Applications

    International Nuclear Information System (INIS)

    Bilderback, Donald H.; Kazimirov, Alexander; Gillilan, Richard; Cornaby, Sterling; Woll, Arthur; Zha, Chang-Sheng; Huang Rong

    2007-01-01

    A number of synchrotron x-ray applications such as powder diffraction in diamond anvil cells, microbeam protein crystallography, x-ray fluorescence imaging, etc. can benefit from using hollow glass monocapillary optics to improve the flux per square micron on a sample. We currently draw glass tubing into the desired elliptical shape so that only one-bounce under total reflection conditions is needed to bring the x-ray beam to a focus at a 25 to 50 mm distance beyond the capillary tip. For modest focal spot sizes of 10 to 20 microns, we can increase the intensity per square micron by factors of 10 to 1000. We show some of the results obtained at CHESS and Hasylab with capillaries focusing 5 to 40 keV radiation, their properties, and how even better the experimental results could be if more ideal capillaries were fabricated in the future

  5. High pressure neutron powder diffraction at LANSCE

    International Nuclear Information System (INIS)

    Von Dreele, R.B.

    1994-01-01

    By making use of the recently developed ''Paris-Edinburgh'' high pressure cell, the author has successfully performed neutron powder experiments to 10GPa at ambient temperature. Results for the structural compression of the high Tc 1223-Hg superconductor to 9.2 GPa, the compression and possible hydrogen bond formation in brucite, Mg(OD) 2 , to 9.3 GPa, and the molecular reorientation in nitromethane to 5.5 GPa will be presented

  6. Acquiring the fundamentals: an accredited powder diffraction course on the internet

    International Nuclear Information System (INIS)

    Crockcroft, J.K.; Barnes, P.; Attfield, M.P.; Cranswick, L.M.D.

    2002-01-01

    Full text: In August 1999, building on accredited academic-based crystallographic web courses pioneered by Birkbeck College, University of London, for Protein Crystallography and Principles of Protein Structure, a new 'Advanced Certificate in Powder Diffraction' was officially announced at the International Union of Crystallography congress in Glasgow. Offering tuition via the Internet on the fundamentals in powder diffraction, it is now running successfully into its third year. The background of student intake ranges from new PhD students to scientists, technicians and X-ray analysts in commercial companies. The work for this 1 year long course, takes around 6 to 8 hours a week to complete; and should not be considered equivalent to recreational web browsing, but as serious study. If this course is done as part of staff training and development, it is important that the employer recognize this; and that adequate training time is set aside as part of the working week. The 'Advanced Certificate in Powder Diffraction' is assessed by a mixture of 'coursework', computer based data analysis project and a formal written exam taken at a local university. To obtain the full qualification, the exam must be taken, but it is optional if only training and no formal qualification is required. The course content covers a broad range of knowledge required for an 'understanding' of powder diffraction. These include the Internet Skills required to do the course, Diffraction Instrumentation, Laboratory Methods, Synchrotron Sources and Methods, Neutron Sources, Diffraction Theory, Electron Scattering to Structure Factors, Structure Factors to Diffraction Intensities, the concept of Symmetry to 3-D Symmetry Elements, Point Groups, Space Groups, Space-Group Determination, Interpreting the IUCr International Tables, Qualitative Analysis, Quantitative Analysis, Indexing, Unit-Cell Refinement, Peak Shapes, Structure Refinement and the Rietveld Method, Modern Techniques and Applications

  7. Analysis Strategy of Powder Diffraction Data with 2-D Detector

    Energy Technology Data Exchange (ETDEWEB)

    Kumar, Abhik; /SLAC, SSRL

    2006-01-25

    To gain a clearer understanding of orientation and grain deformation of crystalline materials, x-ray powder diffraction has played an integral role in extracting three-dimensional structural information from one-dimensional diffraction patterns. Powder diffraction models identical geometry to the intersection of a normal right cone with a plane. The purpose of this paper is to develop a general expression defining the conic sections based on the geometry of a powder diffraction experiment. Applying the derived formulation of a diffraction arc to experimental data will give insight to the molecular and structural properties of the sample in question. Instead of using complex three-dimensional Euclidian geometry, we define the problem solving technique with a simpler two-dimensional transformation approach to arrive at the final equation describing the conic sections. Using the diffraction geometry parameters, we can use this equation to calibrate the diffractometer from the diffraction pattern of a known reference material, or to determine the crystalline lattice structure of the compound.

  8. Applications of neutron powder diffraction in materials research

    International Nuclear Information System (INIS)

    Kennedy, S.J.

    1995-01-01

    The aim of this article is to provide an overview of the applications of neutron powder diffraction in materials science. The technique is described with particular attention to comparison with the X-ray powder diffraction technique to which it is complementary. In this context, emphasis is placed on rapid data acquisition and in-situ studies of phase transitions. Examples of some applications of the technique to materials science problems, at the HIFAR research reactor, Lucas Heights are included. 8 refs., 12 figs

  9. Applications of neutron powder diffraction in materials research

    International Nuclear Information System (INIS)

    Kennedy, S.J.

    1996-01-01

    The aim of this article is to provide an overview of the applications of neutron powder diffraction in materials science. The technique is introduced with particular attention to comparison with the X-ray powder diffraction technique to which it is complementary. The diffractometers and special environment ancillaries operating around the HIFAR research reactor at the Australian Nuclear Science and Technology Organisation (ANSTO) are described. Applications of the technique which the advantage of the unique properties of thermal neutrons have been selected from recent materials studies undertaken at ANSTO

  10. In situ hydration of sulphoaluminate cement mixtures monitored by synchrotron x-ray diffraction

    Energy Technology Data Exchange (ETDEWEB)

    Turrillas, X. [Institut de Ciencia de Materials de Barcelona (ICMAB-CSIC), Barcelona (Spain); Martinez, L.G.; Carvalho, A.M.; Carezzato, G.L. [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil); Rossetto, C.M. [Faculdade de Tecnologia de Sao Paulo (FATEC), SP (Brazil)

    2016-07-01

    Full text: The hydration of calcium sulpho-aluminate cement mixtures was studied in situ by synchrotron X-ray diffraction at the XRD1 beamline of the Laboratorio Nacional de Luz Sincrotron (LNLS) in Campinas, SP. The powder specimens were introduced in borosilicate glass capillary tubes of 0.7 mm of internal diameter and imbued with deionized water. As the hydration reaction is very fast the capillaries were placed on the goniometer and the data collection was started after two minutes of mixing with water. The X-ray energy chosen to get an adequate flux for these short time acquisitions was 12 keV or more precisely 1.033258 Å, determined with polycrystalline corundum standard. Diffraction patterns were collected sequentially every 35 seconds for several hours at temperatures ranging from 40 degC to 55 degC with an accuracy better than 0.1 degC attained with the help of a hot air blower. The diffracted signal was collected with an array of twenty-four Mythen detectors at 760 mm from the capillary tube. The diffraction patterns had appropriate statistics to determine the kinetics of the reaction either by quantitative Rietveld analysis or by fitting isolated diffraction peaks to Gaussian curves as a function of time. The most important phases involved in the hydration are Klein´s salt, also known as Ye’elimite, Ca4(AlO2)6SO4, and gypsum, CaSO4.2H2O to yield Ettringite, Ca6Al2(SO4)3(OH)12 - 26H2O, phase responsible for the mechanical properties. (author)

  11. Design and Optimisation Strategies of Nonlinear Dynamics for Diffraction Limited Synchrotron Light Source

    CERN Document Server

    Bartolini, R.

    2016-01-01

    This paper introduces the most recent achievements in the control of nonlinear dynamics in electron synchrotron light sources, with special attention to diffraction limited storage rings. Guidelines for the design and optimization of the magnetic lattice are reviewed and discussed.

  12. Differential scanning calorimetric and powder X-ray diffraction ...

    Indian Academy of Sciences (India)

    The thermotropic phase transitions and supramolecular structure of NAAEs were investigated by differential scanning calorimetry (DSC) and powder X-ray diffraction (PXRD). Results obtained from DSC studies indicate that the transition temperatures (t), enthalpies ( t) and entropies ( t) exhibit odd-even alternation ...

  13. Structure elucidation of 3-[1-(6-methoxy-2-naphtyl)ethyl]-6-(2,4-dichlorophenyl)-7H-1,2,4-triazolo[3,4-b]-1,3,4-thiadiazine, C23H18Cl2N4OS from synchrotron X-ray powder diffraction

    Energy Technology Data Exchange (ETDEWEB)

    Gündoğdu, Gülsüm; Aytaç, Sevim Peri; Müller, Melanie; Tozkoparan, Birsen; Kaynak, Filiz Betül

    2017-12-01

    The 3-[1-(6-methoxy-2-naphtyl)ethyl]-6-(2,4-dichlorophenyl)-7H-1,2,4-triazolo[3,4-b]-1,3,4-thiadiazine, C23H18Cl2N4OS compound was synthesized, as a member of the family of novel potential anticancer agents. The structure of the title compound was characterized by IR,1H-NMR, mass spectroscopy, and elemental analysis, previously. In this study, the crystal structure of this compound has been determined from synchrotron X-ray powder diffraction data. The crystal structure was solved by simulated annealing and the final structure was achieved by Rietveld refinement method using soft restrains on all interatomic bond lengths and angles. This compound crystallizes in space groupP21,Z= 2, with the unit-cell parametersa= 15.55645(11) Å,b= 8.61693(6) Å,c= 8.56702(6) Å,β= 104.3270(4)°, andV= 1112.68(1) Å3. In the crystal structure, strong C-H∙∙∙πand weak intermolecular hydrogen-bonding interactions link the molecules into a three-dimensional network. The molecules are in a head-to-head arrangement in the unit cell.

  14. High resolution powder diffraction by white source transmission measurements

    International Nuclear Information System (INIS)

    Johnson, R.G.; Bowman, C.D.

    1982-01-01

    Neutron powder diffraction has been studied by measuring the total neutron cross section using neutron time-of-flight in transmission geometry. This method is equivalent to measurements in scattering geometry of powder diffraction at 20 = 180 0 . Measurements on iron samples were conducted using the NBS 100 MeV electron linac as a pulsed neutron source and using flight paths of 20 and 60 meters. The resolution at 60 m for 25-MeV neutrons was limited to dlambda lambda=0.2% primarily by moderator hold-up. Although the change in cross section at the Bragg edges may be quite small, counting rates are high permitting the recording of data with a 0.1% statistical precision in about one day. For the Fe samples, diffraction edges were distinguished as high as n = 196 (where n is the sum of the squares of the Miller indicies) with all edges distinguishable below n = 90

  15. Thermal expansion and phase transformations of nitrogen-expanded austenite studied with in situ synchrotron X-ray diffraction

    DEFF Research Database (Denmark)

    Brink, Bastian; Ståhl, Kenny; Christiansen, Thomas Lundin

    2014-01-01

    as a fitting parameter. The stacking fault density is constant for temperatures up to 680 K, whereafter it decreases to nil. Surprisingly, a transition phase with composition M4N (M = Fe, Cr, Ni, Mo) appears for temperatures above 770 K. The linear coefficient of thermal expansion depends on the nitrogen......Nitrogen-expanded austenite, _N, with high and low nitrogen contents was produced from AISI 316 grade stainless steel powder by gaseous nitriding in ammonia/hydrogen gas mixtures. In situ synchrotron X-ray diffraction was applied to investigate the thermal expansion and thermal stability...

  16. Transmission in situ and operando high temperature X-ray powder diffraction in variable gaseous environments

    Science.gov (United States)

    Schlicker, Lukas; Doran, Andrew; Schneppmüller, Peter; Gili, Albert; Czasny, Mathias; Penner, Simon; Gurlo, Aleksander

    2018-03-01

    This work describes a device for time-resolved synchrotron-based in situ and operando X-ray powder diffraction measurements at elevated temperatures under controllable gaseous environments. The respective gaseous sample environment is realized via a gas-tight capillary-in-capillary design, where the gas flow is achieved through an open-end 0.5 mm capillary located inside a 0.7 mm capillary filled with a sample powder. Thermal mass flow controllers provide appropriate gas flows and computer-controlled on-the-fly gas mixing capabilities. The capillary system is centered inside an infrared heated, proportional integral differential-controlled capillary furnace allowing access to temperatures up to 1000 °C.

  17. Entrainment of lactose inhalation powders: a study using laser diffraction.

    Science.gov (United States)

    Watling, C P; Elliott, J A; Cameron, R E

    2010-07-11

    We have investigated the mechanism of entrainment of lactose inhalation blends released from a dry powder inhaler using a diffraction particle size analyser (Malvern Spraytec). Whether a powder blend entrains as a constant stream of powder (the "erosion" mechanism) or as a few coarse plugs (the "fracture" mechanism) was found by comparing transmission data with particle size information. This technique was then applied to a lactose grade with 0, 5 and 10wt% added fine particles. As the wt% fines increased, the entrainment mechanism was found to change from a mild fracture, consisting of multiple small plugs, to more severe fracture with fewer plugs. The most severe fracture mechanism consisted of either the powder reservoir emptying as a single plug, or of the reservoir emptying after a delay of the order of 0.1s due to the powder sticking to its surroundings. Further to this, three different inhalation grades were compared, and the severity of the fracture was found to be inversely proportional to the flowability of the powder (measured using an annular ring shear tester). By considering the volume of aerosolised fine particles in different blends it was determined that the greater the volume of fines added to a powder, the smaller the fraction of fines that were aerosolised. This was attributed to different behaviour when fines disperse from carrier particles compared with when they disperse from agglomerates of fines. In summary, this paper demonstrates how laser diffraction can provide a more detailed analysis of an inhalation powder than just its size distribution. 2010. Published by Elsevier B.V. All rights reserved.

  18. Fundamentals of powder x-ray diffraction practice

    International Nuclear Information System (INIS)

    Raftery, T.

    2002-01-01

    Full text: The goal of powder Xray diffraction is to gain information about a specimen or sample. Key aspects of this goal are 1. the sample selection, preparation and presentation; 2. the data collection process and conditions; 3. the interaction between these and the interpretation of the data. The 'ideal' powder (or polycrystalline) xray diffraction sample is fine grained, randomly orientated, homogenous and representative. There exists standard sample selection and preparation techniques for powders - sometimes however, the required information must be gained by alternate sample selection and preparation techniques. While there are few variables in the data collection process, there are some significant ones such as matching diffractometer resolution and intensity to the data collection goal whether that is phase identity, quantitative analysis or structure refinement, etc. There are also options of optical arrangement (Bragg-Brintano versus parallel beam versus Debye-Scherrer). One important aspect of the collection process is the assessment of the data quality. Powder xray diffraction has many applications from the straight-forward confirmation of phase identity and purity to structural analysis. Some of these applications will be considered and the interaction between the goal of the application and aspects of sample selection. Copyright (2002) Australian X-ray Analytical Association Inc

  19. Energy-dispersive X-ray diffraction beamline at Indus-2 synchrotron ...

    Indian Academy of Sciences (India)

    Abstract. An energy-dispersive X-ray diffraction beamline has been designed, developed and commissioned at BL-11 bending magnet port of the Indian synchrotron source, Indus-2. The performance of this beamline has been benchmarked by measuring diffraction patterns from var- ious elemental metals and standard ...

  20. Energy-dispersive X-ray diffraction beamline at Indus-2 synchrotron ...

    Indian Academy of Sciences (India)

    An energy-dispersive X-ray diffraction beamline has been designed, developed and commissioned at BL-11 bending magnet port of the Indian synchrotron source, Indus-2. The performance of this beamline has been benchmarked by measuring diffraction patterns from various elemental metals and standard inorganic ...

  1. Neutron powder diffraction under high pressure at J-PARC

    International Nuclear Information System (INIS)

    Utsumi, Wataru; Kagi, Hiroyuki; Komatsu, Kazuki; Arima, Hiroshi; Nagai, Takaya; Okuchi, Takuo; Kamiyama, Takashi; Uwatoko, Yoshiya; Matsubayashi, Kazuyuki; Yagi, Takehiko

    2009-01-01

    It is expected that high-pressure material science and the investigation of the Earth's interior will progress greatly using the high-flux pulse neutrons of J-PARC. In this article, we introduce our plans for in situ neutron powder diffraction experiments under high pressure at J-PARC. The use of three different types of high-pressure devices is planned; a Paris-Edinburgh cell, a new opposed-anvil cell with a nano-polycrystalline diamond, and a cubic anvil high-pressure apparatus. These devices will be brought to the neutron powder diffraction beamlines to conduct a 'day-one' high-pressure experiment. For the next stage of research, we propose construction of a dedicated beamline for high-pressure material science. Its conceptual designs are also introduced here.

  2. Modern trends in x-ray powder diffraction

    International Nuclear Information System (INIS)

    Goebel, H.E.; Snyder, R.L.

    1985-01-01

    The revival of interest in X-ray powder diffraction, being quoted as a metamorphosis from the 'ugly duckling' to a 'beautiful swan', can be attributed to a number of modern developments in instrumentation and evaluation software. They result in faster data collection, improved accuracy and resolution, and better detectability of minor phases. The ease of data evaluation on small computers coupled direct to the instrument allows convenient execution of previously tedious and time-consuming off-line tasks like qualitative and quantitative analysis, characterization of microcrystalline properties, indexing, and lattice-constant refinements, as well as structure refinements or even exploration of new crystal structures. Powder diffraction has also progressed from an isolated analytical laboratory method to an in situ technique for analysing solid-state reactions or for the on-stream control of industrial processes. The paper surveys these developments and their real and potential applications, and tries to emphasize new trends that are regarded as important steps for the further progress of X-ray powder diffraction

  3. Feasibility studies for high pressure neutron powder diffraction experiments

    International Nuclear Information System (INIS)

    Von Dreele, R.B.; Parise, J.

    1990-01-01

    We recently performed two neutron powder diffraction experiments on very small samples on the High Intensity Powder Diffractometer (HIPD). These were done to determine the feasibility of performing in situ high pressure/high temperature neutron diffraction experiments on HIPD at pressures which would exceed the previous limit of ∼50 kbar achievable in a neutron diffraction experiment. The first experiment consisted of examining the product from a high pressure preparation done at Stony Brook. The sample, which had been prepared at 65 kbar and 1000 degree C, consisted of a small platinum capsule filled with CaGeO 3 perovskite. The weights of the capsule included 225 mg of platinum and 49 mg of the germanate. A diffraction experiment taking ∼8.6 hrs at a LANSCE proton beam current of ∼53 μA gave peaks of good intensity from both Pt and CaGeO 3 ; we could begin to see them after only 20 min of beam time. The second experiment was to test the possibility of diffraction from a high pressure apparatus. We placed in the HIPD sample position the central assembly from a 100 kbar octahedral press. Four tungsten carbide anvils and a copper block previously pressed to 65 kbar were held in an aluminum frame. The sample consisted of a small bit of nickel foil (175 mg) placed in a 3 mm hole in the copper block. The active sample volume is defined by the gap between the anvils and the length of the sample. A small portion of the copper block is also seen in this arrangement. This is viewed at 90 degree 2Θ through a similar gap between the anvils by 4 1/2 in. x 12 in. 3 He counter tubes. This arrangement simulates the operating conditions of a high pressure run at 100 kbar and takes advantage of the fixed instrument geometry possible in time-of-flight neutron diffraction experiments

  4. Crystal structure and charge density analysis of Li2NH by synchrotron X-ray diffraction

    International Nuclear Information System (INIS)

    Noritake, T.; Nozaki, H.; Aoki, M.; Towata, S.; Kitahara, G.; Nakamori, Y.; Orimo, S.

    2005-01-01

    Complex hydrides, such as lithium amide (LiNH 2 ) and lithium imide (Li 2 NH), have recently been noticed as one of the most promising materials for reversible hydrogen storage. In this paper, we reveal the bonding nature of hydrogen in Li 2 NH crystal by synchrotron powder X-ray diffraction measurement at room temperature. The crystal structure was refined by Rietveld method and the charge density distribution was analyzed by maximum entropy method (MEM). The Li 2 NH crystal is anti-fluorite type structure (space group Fm3-bar m) consisting of Li and NH. Hydrogen atom occupies randomly the 48h (Wyckoff notation) sites around N atom. The refined lattice constant is a=5.0742(2)A. The charge density distribution around NH anion in Li 2 NH is almost spherical. The number of electrons within the sphere around the Li and NH is estimated from the obtained charge density distribution. As the result, the ionic charge is expressed as [Li 0.99+ ] 2 [NH] 1.21- . Therefore, it is confirmed experimentally that Li 2 NH is ionically bonded

  5. Spinel materials for Li-ion batteries: new insights obtained by operando neutron and synchrotron X-ray diffraction.

    Science.gov (United States)

    Bianchini, Matteo; Fauth, François; Suard, Emmanuelle; Leriche, Jean Bernard; Masquelier, Christian; Croguennec, Laurence

    2015-12-01

    In the last few decades Li-ion batteries changed the way we store energy, becoming a key element of our everyday life. Their continuous improvement is tightly bound to the understanding of lithium (de)intercalation phenomena in electrode materials. Here we address the use of operando diffraction techniques to understand these mechanisms. We focus on powerful probes such as neutrons and synchrotron X-ray radiation, which have become increasingly familiar to the electrochemical community. After discussing the general benefits (and drawbacks) of these characterization techniques and the work of customization required to adapt standard electrochemical cells to an operando diffraction experiment, we highlight several very recent results. We concentrate on important electrode materials such as the spinels Li1 + xMn2 - xO4 (0 ≤ x ≤ 0.10) and LiNi0.4Mn1.6O4. Thorough investigations led by operando neutron powder diffraction demonstrated that neutrons are highly sensitive to structural parameters that cannot be captured by other means (for example, atomic Debye-Waller factors and lithium site occupancy). Synchrotron radiation X-ray powder diffraction reveals how LiMn2O4 is subject to irreversibility upon the first electrochemical cycle, resulting in severe Bragg peak broadening. Even more interestingly, we show for the first time an ordering scheme of the elusive composition Li0.5Mn2O4, through the coexistence of Mn(3+):Mn(4+) 1:3 cation ordering and lithium/vacancy ordering. More accurately written as Li0.5Mn(3+)0.5Mn(4+)1.5O4, this intermediate phase loses the Fd\\overline 3m symmetry, to be correctly described in the P213 space group.

  6. Feasibility studies for high pressure neutron powder diffraction experiments

    International Nuclear Information System (INIS)

    Von Dreele, R.B.

    1991-01-01

    We recently performed two neutron powder diffraction experiments on very small samples on the High Intensity Powder Diffractometer (HIPD), to determine the feasibility of performing in situ high pressure/high temperature neutron diffraction experiments on HIPD at pressures which would exceed the previous limit of ∼50kbar achievable in a neutron diffraction experiment. The sample, which had been prepared at 65kbar and 1000degC, consisted of a small platinum capsule filled with CaGeO 3 perovskite. A diffraction experiment taking ∼8.6hrs at a LANSCE proton beam current of ∼53μA gave peaks of good intensity from both Pt and CaGeO 3 ; we could begin to see them after only 20min if beam time. The second experiment was to test the possibility of diffraction from a high pressure apparatus. We placed in the HIPD sample position the central assembly from a 100kbar octahedral press. Four tungsten carbide anvils and a copper block previously pressed to 65kbar were held in an aluminum frame. The sample consisted of a small bit of nickel foil placed in a 3 mm hole in the copper block. The active sample volume is defined by the gap (∼0.7mm) between the anvils and the length of the sample. A small portion of the copper block is also seen in this arrangement. This is viewed at 90deg 2Θ through a similar gap between the anvils by 4 1/2''x12'' 3 He counter tubes. This arrangement simulates the operating conditions of a high pressure run at 100kbar and takes advantage of the fixed instrument geometry possible in time-of-flight neutron diffraction experiments. We obtained a diffraction pattern in ∼7.1hrs and ∼57μA beam current which clearly showed peaks from both copper and nickel with no evidence of diffraction from the anvils or any other part of the assembly. These two experiments clearly demonstrate the feasibility of performing high pressure in situ diffraction experiments in excess of 100kbar on HIPD at LANSCE. (J.P.N.)

  7. XRAYL: a program for producing idealized powder diffraction line profiles from overlapped powder patterns

    Energy Technology Data Exchange (ETDEWEB)

    Hubbard, C.R.; Morosin, B. [Sandia National Labs., Albuquerque, NM (United States); Stewart, J.M. [Maryland Univ., College Park, MD (United States)

    1996-09-01

    The X-ray diffraction patterns of samples of polycrystalline materials are used to identify and characterize phases. Very often the total (or composite) profile consists of a series of overlapping profiles. In many applications it is necessary to separate the component profiles from the total profile. (In this document the terms {ital profile, line}, and {ital peak} are used interchangeably to represent these features of X-ray or neutron diffraction patterns.) A computer program, XRAYL, first developed in the 1980s and subsequently enlarged and improved, allows the fitting of analytical functions to powder diffraction lines. The fitting process produces parameters of chosen profile functions, diffraction line by diffraction line. The resulting function parameters may then be used to generate ``idealized`` powder diffraction lines as counts at steps in 2{Omega}. The generated lines are effectively free of statistical noise and contributions from overlapping lines. Each separated line extends to background on both sides of the generated profile. XRAYL may, therefore, be used in X-ray powder diffraction profile analysis as a preprocessor program that is, separating peaks and feeding the ``resolved`` data to subsequent analysis programs. This self- contained document includes: (1) a description of the fitting functions coded into XRAYL, (2) an outline of the least-squares algorithm used in fitting the profile function, (3) the file formats and contents utilized by the computer code, (4) the user options and their presentation requirements for execution of the program, (5) an example of input and output for a test case, and (6) source code listings on a diskette.

  8. Synchrotron x-ray diffraction study of liquid surfaces

    DEFF Research Database (Denmark)

    Als-Nielsen, Jens Aage; Pershan, P.S.

    1983-01-01

    A spectrometer for X-ray diffraction and refraction studies of horizontal, free surfaces of liquids is described. As an illustration smetic-A layering at the surface of a liquid crystal is presented.......A spectrometer for X-ray diffraction and refraction studies of horizontal, free surfaces of liquids is described. As an illustration smetic-A layering at the surface of a liquid crystal is presented....

  9. Unit-cell refinement from powder diffraction scans

    International Nuclear Information System (INIS)

    Pawley, G.S.

    1981-01-01

    A procedure for the refinement of the crystal unit cell from a powder diffraction scan is presented. In this procedure knowledge of the crystal structure is not required, and at the end of the refinement a list of indexed intensities is produced. This list may well be usable as the starting point for the application of direct methods. The problems of least-squares ill-conditioning due to overlapping reflections are overcome by constraints. An example using decafluorocyclohexene, C 6 F 10 , shows the quality of fit obtained in a case which may even be a false minimum. The method should become more relevant as powder scans of improved resolution become available, through the use of pulsed neutron sources. (Auth.)

  10. Powder X-ray diffraction study af alkali alanates

    DEFF Research Database (Denmark)

    Cao, Thao; Mosegaard Arnbjerg, Lene; Jensen, Torben René

    Powder X-ray diffraction study of alkali alanates Thao Cao, Lene Arnbjerg, Torben R. Jensen. Center for Materials Crystallography (CMC), Center for Energy Materials (CEM), iNANO and Department of Chemistry, Aarhus University, DK-8000, Denmark. Abstract: To meet the energy demand in the future...... for mobile applications, new materials with high gravimetric and volumetric storage capacity of hydrogen have to be developed. Alkali alanates are promising for hydrogen storage materials. Sodium alanate stores hydrogen reversibly at moderate conditions when catalysed with, e.g. titanium, whereas potassium...

  11. Characterization of Polycrystalline Materials Using Synchrotron X-ray Imaging and Diffraction Techniques

    DEFF Research Database (Denmark)

    Ludwig, Wolfgang; King, A.; Herbig, M.

    2010-01-01

    propagation based phase contrast imaging, a 3-D imaging mode exploiting the coherence properties of third generation synchrotron beams. Furthermore, for some classes of polycrystalline materials, one may use a 3-D variant of x-ray diffraction imaging, termed x-ray diffraction contrast tomography. X-ray......The combination of synchrotron radiation x-ray imaging and diffraction techniques offers new possibilities for in-situ observation of deformation and damage mechanisms in the bulk of polycrystalline materials. Minute changes in electron density (i.e., cracks, porosities) can be detected using...... diffraction contrast tomography provides access to the 3-D shape, orientation, and elastic strain state of the individual grains from polycrystalline sample volumes containing up to thousand grains. Combining both imaging modalities, one obtains a comprehensive description of the materials microstructure...

  12. Characterization of Polycrystalline Materials Using Synchrotron X-ray Imaging and Diffraction Techniques

    DEFF Research Database (Denmark)

    Ludwig, Wolfgang; King, A.; Herbig, M.

    2010-01-01

    The combination of synchrotron radiation x-ray imaging and diffraction techniques offers new possibilities for in-situ observation of deformation and damage mechanisms in the bulk of polycrystalline materials. Minute changes in electron density (i.e., cracks, porosities) can be detected using...... propagation based phase contrast imaging, a 3-D imaging mode exploiting the coherence properties of third generation synchrotron beams. Furthermore, for some classes of polycrystalline materials, one may use a 3-D variant of x-ray diffraction imaging, termed x-ray diffraction contrast tomography. X......-ray diffraction contrast tomography provides access to the 3-D shape, orientation, and elastic strain state of the individual grains from polycrystalline sample volumes containing up to thousand grains. Combining both imaging modalities, one obtains a comprehensive description of the materials microstructure...

  13. The storage degradation of an 18650 commercial cell studied using neutron powder diffraction

    Science.gov (United States)

    Lee, Po-Han; Wu, She-huang; Pang, Wei Kong; Peterson, Vanessa K.

    2018-01-01

    Commercial 18650 lithium ion cells containing a blended positive electrode of layered LiNi0.5Mn0.3Co0.2O2 and spinel Li1.1Mn1.9O4 alongside a graphite negative electrode were stored at various depth-of-discharge (DoD) at 60 °C for 1, 2, 4, and 6 months. After storage, the cells were cycled at C/25 at 25 °C between 2.75 and 4.2 V for capacity determination and incremental capacity analysis (ICA). In addition to ICA analysis, the mechanism for capacity fade was investigated by combining the results of neutron powder diffraction under in-situ and operando conditions, in conjunction with post-mortem studies of the electrodes using synchrotron X-ray powder diffraction and inductively-coupled plasma optical emission spectroscopy. Among the cells, those stored at 25% DoD suffered the highest capacity fade due to their higher losses of active Li, NMC, and LMO than cells stored at other DoD. The cells stored at 0% DoD shows second high capacity fade because they exhibit the highest of active LMO and graphite anode among the stored cells and higher losses of active Li and NMC than cells stored at 50% DoD.

  14. Solving a superstructure from two-wavelength x-ray powder diffraction data - a simulation

    Science.gov (United States)

    Chen, Jian-Rong; Gu, Yuan-Xin; Fan, Hai-Fu

    2003-03-01

    Two different kinds of phase ambiguities are intrinsic in two-wavelength x-ray powder diffraction from acentric crystal structures having pseudo-translation symmetry. In a test calculation we have solved the problem for the first time by two different phasing procedures developed originally in single-crystal structure analysis. They are the direct method of breaking enantiomorphous phase ambiguity in protein crystallography and that of breaking translational phase ambiguity for superstructures. An artificial structure was used in the test, which is based on atomic coordinates of the known structure, SHAS (C5H6O5N3K), with the atom K replaced by Rb. The arrangement of Rb atoms possesses a subperiodicity of t = (a + b + c)/2. Two-wavelength synchrotron x-ray powder diffraction data were simulated with lambda1=0.0816nm and lambda2=0.1319nm. Overlapped reflections were uniformly decomposed at the beginning and redecomposed afterward when the partial-structure information became available. The enantiomorphous phase ambiguity was resolved only for reflections with h + k + l even. Phases of reflections with h + k + l odd were derived by the direct method of solving superstructures. A fragment was then obtained, which led to the complete structure in five cycles of Fourier iteration.

  15. Comparative study of structural properties of trehalose water solutions by neutron diffraction, synchrotron radiation and simulation

    Energy Technology Data Exchange (ETDEWEB)

    Cesaro, A.; Magazu, V.; Migliardo, F.; Sussich, F.; Vadala, M

    2004-07-15

    Neutron diffraction measurements combined with H/D substitution have been performed on trehalose aqueous solutions as a function of temperature and concentration by using the SANDALS diffractometer at ISIS Facility (UK). The findings point out a high capability of trehalose to strongly affect the tetrahedral hydrogen bond network of water. The neutron diffraction results are also compared with simulation and experimental data obtained by synchrotron radiation on the phospholipid bilayer membranes (DPPC)/trehalose/H{sub 2}O ternary system.

  16. The CCP14 for single crystal and powder diffraction

    International Nuclear Information System (INIS)

    Cranswick, L.M.D.

    1999-01-01

    Full text: The Collaborative Computation Project Number 14 for Single Crystal and Powder Diffraction (CCP14) is continuing in its objective to provide freely available software and resources for the powder diffraction and crystallographic community. Using the Internet and World Wide Web, we are presently compiling software and web resources, creating tutorials and help files. It also endeavours to encourage and provide resources to assist program authors with developing their software. The CCP14 presently has its web-site at and a mirror at (at CSIRO, Melbourne, Australia). Auto web-mirroring is being implemented to allow users to obtain software and access to resources in a more time effective manner. For people in countries isolated from the Internet, the CCP14 on CD-ROM can be snail mailed on request. This is in the form of a Virtual World Wide Web/Virtual Internet; in the same vein as the existing Crystallographic Nexus CD-ROM. Copyright (1999) Australian X-ray Analytical Association Inc

  17. Synchrotron WAXS and XANES studies of silica (SiO2) powders synthesized from Indonesian natural sands

    International Nuclear Information System (INIS)

    Muchlis, Khairanissa; Fauziyah, Nur Aini; Pratapa, Suminar; Soontaranon, Siriwat; Limpirat, Wanwisa

    2017-01-01

    In this study, we have investigated polymorphic silica (SiO 2 ) powders using, Wide Angle X-ray Scattering (WAXS) and X-Ray Absorption Near Edge Spectroscopy (XANES), laboratory X-Ray Diffraction (XRD) instruments. The WAXS and XANES spectra were collected using synchrotron radiation at Synchrotron Light Research Institute (SLRI), Nakhon Ratchasima, Thailand. The silica powders were obtained by processing silica sand from Tanah Laut, South Kalimantan, Indonesia. Purification process of silica sand was done by magnetic separation and immersion with HCl. The purification step was needed to reduce impurity or undesirable non Si elements. Three polymorphs of silica were produced, i.e. amorphous phase (A), quartz (B), and cristobalite (C). WAXS profile for each phase was presented in terms of intensity vs. 2θ prior to analyses. Both XRD (λ CuKα =1.54056 Å) and WAXS (λ=1.09 Å) patttern show that (1) A sample contains no crystallites, (2) B sample is monophasic, contains only quartz, and (3) C sample contains cristobalite and trydimite. XRD quantitative analysis using Rietica gave 98,8 wt% cristobalite, while the associated WAXS data provided 98.7 wt% cristobalite. Si K-edge XANES spectra were measured at energy range 1840 to 1920 eV. Qualitatively, the pre-edge and edge features for all phases are similar, but their main peaks in the post-edge region are different. (paper)

  18. Maximum Entropy Method for neutron powder diffraction data

    International Nuclear Information System (INIS)

    Sakata, Makoto; Uno, Tatsuya; Takata, Masaki; Takagi, Masahiro; Kumazawa, Shintaro; Howard, C.J.

    1993-01-01

    The Maximum Entropy Method (MEM) is powerful method to restore the accurate electron density distribution from X-ray diffraction data. It deals with electron density which is always positive. In order to analyze neutron diffraction data by the MEM, it is necessary to overcome the difficulty of negative scattering length of some atoms, such as Ti, Mn. In this work, a new approach to solving the negative scattering problem is described. It is based on nuclear densities rather than densities of scattering length, because the nuclear densities are always positive. The new method is successfully applied to analyze the neutron powder data from two polymorphs of TiO 2 , i.e. rutile and anatase. The procedure, like its X-ray counter-part, requires no structural model. The nuclear densities of rutile obtained by the present method is compared with the electron density distribution previously obtained by the MEM analysis. In contrast to the electron density distribution, nuclear densities show completely no density between Ti and O nuclei. It is also revealed that both Ti and O nuclear densities are confined within a very limited space. The present analysis provide a good demonstration of complementary nature of neutron and X-ray diffraction. (author)

  19. Synchrotron X-ray and neutron diffraction studies in solid-state chemistry

    International Nuclear Information System (INIS)

    Cheetham, A.K.; Wilkinson, A.P.

    1992-01-01

    Since the scatterers are different - X-rays are scattered by the electrons of an atom, neutrons by the nuclei - the questions addressed by the two diffraction experiments have been complementary. For example, neighboring elements of the periodic table could be distinguished formerly only by neutron diffraction. Now, however, this is also partly possible with high-energy synchrotron radiation. This review describes recent applications of X-ray and neutron diffraction methods in solid-state chemistry and how the maximal information can be extracted by a combination of techniques. (orig.)

  20. Synchrotron X-Ray Reciprocal Space Mapping, Topography and Diffraction Resolution Studies of Macromolecular Crystal Quality

    Science.gov (United States)

    Boggon, T. J.; Helliwell, J. R.; Judge, Russell A.; Siddons, D. P.; Snell, Edward H.; Stojanoff, V.

    2000-01-01

    A comprehensive study of microgravity and ground grown chicken egg white lysozyme crystals is presented using synchrotron X-ray reciprocal space mapping, topography techniques and diffraction resolution. Microgravity crystals displayed, on average, reduced intrinsic mosaicities but no differences in terms of stress over their earth grown counterparts. Topographic analysis revealed that in the microgravity case the majority of the crystal was contributing to the peak of the reflection at the appropriate Bragg angle. In the earth case at the diffraction peak only a small volume of the crystal contributed to the intensity. The techniques prove to be highly complementary with the reciprocal space mapping providing a quantitative measure of the crystal mosaicity and stress (or variation in lattice spacing) and topography providing a qualitative overall assessment of the crystal in terms of its X-ray diffraction properties. Structural data collection was also carried out both at the synchrotron and in the laboratory.

  1. Mechanically activated SHS reaction in the Fe-Al system: in-situ time resolved diffraction using synchrotron radiation

    International Nuclear Information System (INIS)

    Gaffet, E.; Charlot, F.; Klein, D.; Bernard, F.; Niepce, J.C.

    1998-01-01

    The mechanical activation self propagating high temperature synthesis (M.A.S.H.S.) processing is a new way to produce nanocrystalline iron aluminide intermetallic compounds. This process is maily the combination of two steps; in the one hand, a mechanical activation where the Fe - Al powder mixture was milled during a short time at given energy and frequency of shocks and in the other hand, a self propagating high temperature synthesis (S.H.S.) reaction, for which the exothermicity of the Fe + Al reaction is used. This fast propagated MASHS reaction has been in-situ investigated using the time resolved X-ray diffraction (TRXRD) using a X-ray synchrotron beam and an infrared thermography camera, allowing the coupling of the materials structure and the temperature field. The effects of the initial mean compositions, of the milling conditions as well as of the compaction parameters on the MASHS reaction are reported. (orig.)

  2. Structure solution from powder neutron and x-ray diffraction data: getting the best of both worlds

    International Nuclear Information System (INIS)

    Hunter, B.A.

    2000-01-01

    Full text: Powder diffraction methods have traditionally been used in three main areas: phase identification and quantification, lattice parameter determination and structure refinement. Until recently structure solution has been the almost exclusive domain of single crystal diffraction methods, predominantly using x-rays. The increasing use of synchrotron and neutron sources, and the unrelenting advances in computing hardware and software means that powder methods are challenging single crystal methods as a practical method for structure solution, especially when single crystal method can not be applied. It is known that structural refinements from a known starting structure using combined X-ray and neutron data sets are capable of providing highly accurate structures. Likewise, using combined x-ray and neutron powder diffraction data in the structure solution process should also be a powerful technique, although to date no one is pursuing this methodology. This paper present examples of solutions to the problem. Namely we are using high resolution powder X-ray and neutron methods to solve the structures of molecular materials and minerals, then refining the structures using both sets of data. In this way we exploit the advantages of both methods while minimising the disadvantages. We present our solution for a small amino acid structure, a metalorganic and a mineral structure

  3. Powder X-ray diffraction laboratory, Reston, Virginia

    Science.gov (United States)

    Piatak, Nadine M.; Dulong, Frank T.; Jackson, John C.; Folger, Helen W.

    2014-01-01

    The powder x-ray diffraction (XRD) laboratory is managed jointly by the Eastern Mineral and Environmental Resources and Eastern Energy Resources Science Centers. Laboratory scientists collaborate on a wide variety of research problems involving other U.S. Geological Survey (USGS) science centers and government agencies, universities, and industry. Capabilities include identification and quantification of crystalline and amorphous phases, and crystallographic and atomic structure analysis for a wide variety of sample media. Customized laboratory procedures and analyses commonly are used to characterize non-routine samples including, but not limited to, organic and inorganic components in petroleum source rocks, ore and mine waste, clay minerals, and glassy phases. Procedures can be adapted to meet a variety of research objectives.

  4. High-resolution neutron powder-diffraction in CMR manganates

    Energy Technology Data Exchange (ETDEWEB)

    Suard, E.; Radaelli, P.G. [Institut Max von Laue - Paul Langevin (ILL), 38 - Grenoble (France)

    1997-04-01

    Manganese-oxide materials have recently been the subject of renewed attention, due to the `colossal` magnetoresistance (CMR) displayed near the spin-ordering temperature T{sub c} by some of these compounds. CMR has been evidenced in at least three families of manganese oxides. In most cases, the CMR compounds behave as paramagnetic semiconductors at high temperatures, and as ferromagnetic metals below T{sub c}. The study of this metallization process has lead some theorists to challenge its traditional interpretation in terms of the so-called double-exchange mechanism, and to propose alternative scenarios in which the coupling of the charge carriers with the lattice plays a paramount role. Powder diffraction method, being at the forefront of CMR research is presented. (author). 4 refs.

  5. Examination of Short- and Long-Range Atomic Order Nanocrystalline SiC and Diamond by Powder Diffraction Methods

    Science.gov (United States)

    Palosz, B.; Grzanka, E.; Stelmakh, S.; Gierlotka, S.; Weber, H.-P.; Proffen, T.; Palosz, W.

    2002-01-01

    The real atomic structure of nanocrystals determines unique, key properties of the materials. Determination of the structure presents a challenge due to inherent limitations of standard powder diffraction techniques when applied to nanocrystals. Alternate methodology of the structural analysis of nanocrystals (several nanometers in size) based on Bragg-like scattering and called the "apparent lattice parameter" (alp) is proposed. Application of the alp methodology to examination of the core-shell model of nanocrystals will be presented. The results of application of the alp method to structural analysis of several nanopowders were complemented by those obtained by determination of the Atomic Pair Distribution Function, PDF. Based on synchrotron and neutron diffraction data measured in a large diffraction vector of up to Q = 25 Angstroms(exp -1), the surface stresses in nanocrystalline diamond and SiC were evaluated.

  6. Acemetacin cocrystal structures by powder X-ray diffraction

    Directory of Open Access Journals (Sweden)

    Geetha Bolla

    2017-05-01

    Full Text Available Cocrystals of acemetacin drug (ACM with nicotinamide (NAM, p-aminobenzoic acid (PABA, valerolactam (VLM and 2-pyridone (2HP were prepared by melt crystallization and their X-ray crystal structures determined by high-resolution powder X-ray diffraction. The powerful technique of structure determination from powder data (SDPD provided details of molecular packing and hydrogen bonding in pharmaceutical cocrystals of acemetacin. ACM–NAM occurs in anhydrate and hydrate forms, whereas the other structures crystallized in a single crystalline form. The carboxylic acid group of ACM forms theacid–amide dimer three-point synthon R32(9R22(8R32(9 with three different syn amides (VLM, 2HP and caprolactam. The conformations of the ACM molecule observed in the crystal structures differ mainly in the mutual orientation of chlorobenzene fragment and the neighboring methyl group, being anti (type I or syn (type II. ACM hydrate, ACM—NAM, ACM–NAM-hydrate and the piperazine salt of ACM exhibit the type I conformation, whereas ACM polymorphs and other cocrystals adopt the ACM type II conformation. Hydrogen-bond interactions in all the crystal structures were quantified by calculating their molecular electrostatic potential (MEP surfaces. Hirshfeld surface analysis of the cocrystal surfaces shows that about 50% of the contribution is due to a combination of strong and weak O...H, N...H, Cl...H and C...H interactions. The physicochemical properties of these cocrystals are under study.

  7. X-Ray Powder Diffraction with Guinier - Haegg Focusing Cameras

    International Nuclear Information System (INIS)

    Brown, Allan

    1970-12-01

    The Guinier - Haegg focusing camera is discussed with reference to its use as an instrument for rapid phase analysis. An actual camera and the alignment procedure employed in its setting up are described. The results obtained with the instrument are compared with those obtained with Debye - Scherrer cameras and powder diffractometers. Exposure times of 15 - 30 minutes with compounds of simple structure are roughly one-sixth of those required for Debye - Scherrer patterns. Coupled with the lower background resulting from the use of a monochromatic X-ray beam, the shorter exposure time gives a ten-fold increase in sensitivity for the detection of minor phases as compared with the Debye - Scherrer camera. Attention is paid to the precautions taken to obtain reliable Bragg angles from Guinier - Haegg film measurements, with particular reference to calibration procedures. The evaluation of unit cell parameters from Guinier - Haegg data is discussed together with the application of tests for the presence of angle-dependent systematic errors. It is concluded that with proper calibration procedures and least squares treatment of the data, accuracies of the order of 0.005% are attainable. A compilation of diffraction data for a number of compounds examined in the Active Central Laboratory at Studsvik is presented to exemplify the scope of this type of powder camera

  8. Apparatus development for high-pressure X-ray diffraction using synchrotron radiation

    International Nuclear Information System (INIS)

    Martinez, L.G.; Orlando, M.T.D.; Rossi, J.L.; Passamai Junior, J.L.; Melo, F.C.L.; Ferreira, F.F.

    2006-01-01

    Some phenomena in the field of condensed matter physics can be studied when the matter is submitted to extreme conditions of pressure, magnetic fields or temperatures. Once submitted to these conditions it is generally necessary to measure the properties of the matter in situ. The existence of a synchrotron light laboratory in Brazil opens up the chance of studying materials in extreme conditions by techniques like X-ray diffraction and absorption. However, when compared to high-energy synchrotrons accelerators, the Brazilian source offers a narrower energy range and lower flux. These facts impose limitation to perform diffraction experiments by energy dispersion and, consequently, the use of pressure cells with denser anvils like diamond. However, for a lower-pressure range, preliminary studies showed the viability of measurements in an angular dispersion configuration. This allows the use of silicon carbide anvils B 4C . In this work it is described the development of a hydrostatic pressure cell suitable for X-rays diffraction measurements in the Brazilian Synchrotron Light Laboratory using materials and technologies developed by the institutions and researchers involved in this project (IPEN, UFES, CTA and LNLS). This development can provide the scientific community with the possibility of performing X-ray diffraction measurements under hydrostatic pressure, initially up to 2 GPa, with possibilities of increasing the maximum pressure to higher values, with or without application of magnetic fields and high or low temperatures. (author)

  9. A sample holder for in-house X-ray powder diffraction studies of protein powders

    DEFF Research Database (Denmark)

    Frankær, Christian Grundahl; Harris, Pernille; Ståhl, Kenny

    2011-01-01

    A sample holder for handling samples of protein for in-house X-ray powder diffraction (XRPD) analysis has been made and tested on lysozyme. The use of an integrated pinhole reduced the background, and good signal-to-noise ratios were obtained from only 7 l of sample, corresponding to approximately...... 2-3 mg of dry protein. The sample holder is further adaptable to X-ray absorption spectroscopy (XAS) measurements. Both XRPD and XAS at the Zn K-edge were tested with hexameric Zn insulin....

  10. Powder diffraction. The Rietveld method and the two-stage method to determine and refine crystal structures for powder diffraction data

    International Nuclear Information System (INIS)

    Will, G.

    2006-01-01

    Crystal structure analysis from powder diffraction data has attracted considerable and ever growing interest in the last decades. X-ray powder diffraction is best known for phase analysis (Hanawalt files) dating back to the 30s. In the late 60s the inherent potential of powder diffraction for crystallographic problems was realized and scientists developed methods for using powder diffraction data at first only for the refinement of crystal structures. With the development of ever growing computer power profile fitting and pattern decomposition allowed to extract individual intensities from overlapping diffraction peaks opening the way to many other applications, especially to ab initio structure determination. Powder diffraction today is used in X-ray and neutron diffraction, where it is a powerful method in neutron diffraction for the determination of magnetic structures. In the last decade the interest has dramatically improved. There is hardly any field of crystallography where the Rietveld, or full pattern method has not been tried with quantitative phase analysis the most important recent application. (orig.)

  11. IL 12: Femtosecond x-ray powder diffraction

    International Nuclear Information System (INIS)

    Woerner, M.; Zamponi, F.; Rothhardt, P.; Ansari, Z.; Dreyer, J.; Freyer, B.; Premont-Schwarz, M.; Elsaesser, T.

    2010-01-01

    A chemical reaction generates new compounds out of one or more initial species. On a molecular level, the spatial arrangement of electrons and nuclei changes. While the structure of the initial and the product molecules can be measured routinely, the transient structures and molecular motions during a reaction have remained unknown in most cases. This knowledge, however, is a key element for the exact understanding of the reaction. The ultimate dream is a 'reaction microscope' which allows for an in situ imaging of the molecules during a reaction. We report on the first femtosecond x-ray powder diffraction experiment in which we directly map the transient electronic charge density in the unit cell of a crystalline solid with 30 pico-meter spatial and 100 femtosecond temporal resolution. X-ray diffraction from polycrystalline powder samples, the Debye Scherrer diffraction technique, is a standard method for determining equilibrium structures. The intensity of the Debye Scherrer rings is determined by the respective x-ray structure factor which represents the Fourier transform of the spatial electron density. In our experiments, the transient intensity and angular positions of up to 20 Debye Scherrer reactions from a polycrystalline powder are measured and unravel for the first time a concerted electron and proton transfer in hydrogen-bonded ionic (NH 4 ) 2 SO 4 crystals. Photoexcitation of ammonium sulfate induces a sub-100 fs electron transfer from the sulfate groups into a highly conned electron channel along the z-axis of the unit cell. The latter geometry is stabilized by transferring protons from the adjacent ammonium groups into the channel. Time-dependent charge density maps derived from the diffraction data display a periodic modulation of the channels charge density by low-frequency lattice motions with a concerted electron and proton motion between the channel and the initial proton binding site. A deeper insight into the underlying microscopic

  12. Synchrotron diffraction characterization of nanostructured KY{sub 3}F{sub 10}:Tb

    Energy Technology Data Exchange (ETDEWEB)

    Ichikawa, Rodrigo U.; Teixeira, Maria I.; Ranieri, Izilda M.; Martinez, Luis G., E-mail: ichikawa@usp.br, E-mail: miteixeira@ipen.br, E-mail: iranieri@ipen.br, E-mail: lgallego@ipen.br [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil); Linhares, Horacio M.S.M.D., E-mail: horacio_marconi@yahoo.com.br [Universidade Federal Fluminense (INFES/UFF), Santo Antonio de Padua, RJ (Brazil); Turrillas, Xavier, E-mail: turrillas@gmail.com [Institut de Ciència de Materials de Barcelona (ICMAB/CSIC), Dept. of Crystallography, Bellaterra (Spain)

    2015-07-01

    Nanostructured rare-earth fluorides materials are being intensively studied recently due to their potential applications in high-dose dosimetry. Particularly, nanostructured Tb-doped KY{sub 3}F{sub 10} has shown satisfactory results to be used in this area. In the present work, the structure and microstructure of KY{sub 3}F{sub 10}:Tb was investigated by means of X-ray synchrotron diffraction. One of the samples was analyzed as synthesized and another after a heat treatment. Rietveld refinement of synchrotron diffraction data was applied to obtain cell parameters, atomic positions and atomic displacement factors and the results were compared to values found in literature. X-ray line profile analysis methods were applied to determine mean crystallite sizes and their distribution. (author)

  13. Model experiment of in vivo synchrotron X-ray diffraction of human kidney stones

    Energy Technology Data Exchange (ETDEWEB)

    Ancharov, A.I. [Institute of Solid State Chemistry and Mechanochemistry SB RAS, Novosibirsk (Russian Federation)]. E-mail: ancharov@mail.ru; Potapov, S.S. [Institute of Mineralogy UB RAS, Miass (Russian Federation); Moiseenko, T.N. [The State Regional Clinical Hospital, Novosibirsk (Russian Federation); Feofilov, I.V. [The State Regional Clinical Hospital, Novosibirsk (Russian Federation); Nizovskii, A.I. [Boreskov Institute of Catalysis SB RAS, Novosibirsk (Russian Federation)

    2007-05-21

    The diffraction of synchrotron radiation (SR) was used to explore the phase composition of kidney stones placed into a specific object phantom, which imitated the human body. As an imitation of the patient breath, the kidney stone was moved vertically and rotated to an angle of 15{sup o} during the recording of the X-ray pattern. It was shown that rotation and displacement did not distort the X-ray pattern.

  14. A Furnace for Diffraction Studies using Synchrotron X-Ray Radiation

    DEFF Research Database (Denmark)

    Buras, B.; Lebech, Bente; Kofoed, W.

    1984-01-01

    A furnace for diffraction studies using synchrotron X-ray radiation is described. The furnace can be operated between ambient temperature and 1 800 °C with a temperature stability better than 5 °C for temperatures above 300 °C. Kapton windows allow almost 360° access for the X-ray beam in the hor...... in the horizontal scattering plane and the furnace may be used in both conventional monochromatic beam angle-dispersive and white-beam energy-dispersive diffraction experiments. Details of the furnace windows, heating element, thermometry and sample mount are given....

  15. Structural anomalies in undoped Gallium Arsenide observed in high resolution diffraction imaging with monochromatic synchrotron radiation

    Science.gov (United States)

    Steiner, B.; Kuriyama, M.; Dobbyn, R. C.; Laor, U.; Larson, D.; Brown, M.

    1988-01-01

    Novel, streak-like disruption features restricted to the plane of diffraction have recently been observed in images obtained by synchrotron radiation diffraction from undoped, semi-insulating gallium arsenide crystals. These features were identified as ensembles of very thin platelets or interfaces lying in (110) planes, and a structural model consisting of antiphase domain boundaries was proposed. We report here the other principal features observed in high resolution monochromatic synchrotron radiation diffraction images: (quasi) cellular structure; linear, very low-angle subgrain boundaries in (110) directions, and surface stripes in a (110) direction. In addition, we report systematic differences in the acceptance angle for images involving various diffraction vectors. When these observations are considered together, a unifying picture emerges. The presence of ensembles of thin (110) antiphase platelet regions or boundaries is generally consistent not only with the streak-like diffraction features but with the other features reported here as well. For the formation of such regions we propose two mechanisms, operating in parallel, that appear to be consistent with the various defect features observed by a variety of techniques.

  16. Modelling the X-ray powder diffraction of nitrogen-expanded austenite using the Debye formula

    DEFF Research Database (Denmark)

    Oddershede, Jette; Christiansen, Thomas; Ståhl, Kenny

    2008-01-01

    Stress-free and homogeneous samples of nitrogen-expanded austenite, a defect-rich f.c.c. structure with a high interstitial nitrogen occupancy (between 0.36 and 0.61), have been studied using X-ray powder diffraction and Debye simulations. The simulations confirm the presence of deformation...... to be indistinguishable to X-ray powder diffraction....

  17. Structural and microstructural changes during anion exchange of CoAl layered double hydroxides: an in situ X-ray powder diffraction study

    DEFF Research Database (Denmark)

    Johnsen, Rune; Krumeich, Frank; Norby, Poul

    2010-01-01

    Anion-exchange processes in cobalt-aluminium layered double hydroxides (LDHs) were studied by in situ synchrotron X-ray powder diffraction (XRPD). The processes investigated were CoAl-CO3 CoAl-Cl CoAl-CO3, CoAl-Cl CoAl-NO3 and CoAl-CO3 CoAl-SO4. The XRPD data show that the CoAl-CO3 CoAl-Cl process...

  18. The progress of neutron powder diffraction in J-PARC

    International Nuclear Information System (INIS)

    Ishigaki, Toru

    2007-01-01

    Ibaraki prefecture, the local government of the area for J-PARC site, has decided to build a versatile powder diffractometer (IBARAKI Materials Design Diffractometer) to promote industrial applications for neutron beams in J-PARC. This diffractometer is designed to be a high throughput one enabling materials scientists to use it like the chemical analytical instruments in their material development processes. It covers in d range 0.18 < d(A) < 2.5 with d/d=0.16% at the high resolution scattering detector bank, and covers 2.5 < d(A) < 400 with gradually changing resolution with the standard mode. Typical measurement time to obtain a 'Rietveld-quality' data is several minutes for the sample size of laboratory X-ray diffractometer. To promote industrial application, a utilization system for this diffractometer is required. We will establish a support system for both academic and industrial users who are willing to use neutron but have not been familiar with neutron diffraction. (author)

  19. Diffraction measurements of residual macrostress and microstress using x-rays, synchrotron and neutrons

    International Nuclear Information System (INIS)

    Tanaka, Keisuke; Akiniwa, Yoshiaki

    2004-01-01

    The present paper reviews some recent developments of the measurements of the macrostress and microstress by diffraction using X-rays, synchrotron and neutrons especially in Japan. These three methods are based on the same principle of the diffraction of crystals, and have different advantages. The conventional X-rays detect the stress very near the surface, while the neutron diffraction takes the stress in the interior of the materials. High-energy X-rays from synchrotron sources have the penetration depth in between and are suitable for the measurement of subsurface stresses. After describing the developments of the fundamentals of the methods, the paper covers the recent applications of the diffraction methods to the residual stress analysis in textured thin films, the nondestructive determination of the subsurface distribution of residual stress in shot-peened materials, local stress measurements near the crack tip, the stress measurements of single crystals, macrostress and microstress measurements in composites, and the determination of the internal distribution of the residual stress in welded joints. (author)

  20. Synchrotron Diffraction Studies of Spontaneous Magnetostriction in Rare Earth Transition Metal Compounds

    International Nuclear Information System (INIS)

    Ning Yang

    2004-01-01

    Thermal expansion anomalies of R 2 Fe 14 B and R 2 Fe 17 C x (x = 0,2) (R Y, Nd, Gd, Tb, Er) stoichiometric compounds are studied with high-energy synchrotron X-ray powder diffraction using Debye-Schemer geometry in temperature range 10K to 1000K. Large spontaneous magnetostriction up to their Curie temperatures (T c ) is observed. The a-axes show relatively larger invar effects than c-axes in the R 2 Fe 14 B compounds whereas the R 2 Fe 17 C x show the contrary anisotropies. The iron sub-lattice is shown to dominate the spontaneous magnetostriction of the compounds. The contribution of the rare earth sublattice is roughly proportional to the spin magnetic moment of the rare earth in the R 2 Fe 14 B compounds but in R 2 Fe 17 C x , the rare earth sub-lattice contribution appears more likely to be dominated by the local bonding. The calculation of spontaneous magnetostrain of bonds shows that the bonds associated with Fe(j2) sites in R 2 Fe 14 B and the dumbbell sites in R 2 Fe 17 C x have larger values, which is strongly related to their largest magnetic moment and Wigner-Seitz atomic cell volume. The roles of the carbon atoms in increasing the Curie temperatures of the R 2 Fe 17 compounds are attributed to the increased separation of Fe hexagons. The R 2 Fe 17 and R 2 Fe 14 B phases with magnetic rare earth ions also show anisotropies of thermal expansion above T c . For R 2 Fe 17 and R 2 Fe 14 B the a a /a c > 1 whereas the anisotropy is reversed with the interstitial carbon in R 2 Fe 17 . The average bond magnetostrain is shown to be a possible predictor of the magnetic moment of Fe sites in the compounds. Both of the theoretical and phenomenological models on spontaneous magnetostriction are discussed and a Landau model on the spontaneous magnetostriction is proposed

  1. Progress in X-ray synchrotron diffraction studies of muscle contraction. Ch. 19

    International Nuclear Information System (INIS)

    Wakabayashi, Katsuzo

    1991-01-01

    This chapter provides a review of applications of synchrotron radiation (SR) to X-ray diffraction studies on the dynamic aspects of muscle contraction and is, at the same time, a progress report on the technical developments specifically related to muscle research. The introduction of SR as an intense X-ray source and the development of high ability detectors have led to enormous improvement in the quality of data from time-resolved X-ray diffraction studies of muscle contraction. The X-ray diffraction pattern taken during contraction shows that the force generation of a muscle proceeds upon interaction of the incommensurate structures of the thin and thick filaments. In this framework a distinct intensity change of the weaker reflections from the thin filaments was detected. However, there was still no strong evidence of direct physical attachment of myosin heads to actin during contraction. (author). 170 refs.; 52 figs.; 3 tabs

  2. Monitoring protein precipitates by in-house X-ray powder diffraction

    OpenAIRE

    Ståhl, Kenny; Frankær, Christian Grundahl; Petersen, Jakob; Harris, Pernille

    2013-01-01

    Powder diffraction from protein powders using in-house diffractometers is an effective tool for identification and monitoring of protein crystal forms and artifacts. As an alternative to conventional powder diffractometers a single crystal diffractometer equipped with an X-ray micro-source can be used to collect powder patterns from 1 l samples. Using a small-angle X-ray scattering (SAXS) camera it is possible to collect data within minutes. A streamlined program has been developed for the ca...

  3. Use of synchrotron-based diffraction-enhanced imaging for visualization of soft tissues in invertebrates

    International Nuclear Information System (INIS)

    Rao, Donepudi V.; Swapna, Medasani; Cesareo, Roberto; Brunetti, Antonio; Zhong, Zhong; Akatsuka, Takao; Yuasa, Tetsuya; Takeda, Tohoru; Gigante, Giovanni E.

    2010-01-01

    Images of terrestrial and marine invertebrates (snails and bivalves) have been obtained by using an X-ray phase-contrast imaging technique, namely, synchrotron-based diffraction-enhanced imaging. Synchrotron X-rays of 20, 30 and 40 keV were used, which penetrate deep enough into animal soft tissues. The phase of X-ray photons shifts slightly as they traverse an object, such as animal soft tissue, and interact with its atoms. Biological features, such as shell morphology and animal physiology, have been visualized. The contrast of the images obtained at 40 keV is the best. This optimum energy provided a clear view of the internal structural organization of the soft tissue with better contrast. The contrast is higher at edges of internal soft-tissue structures. The image improvements achieved with the diffraction-enhanced imaging technique are due to extinction, i.e., elimination of ultra-small-angle scattering. They enabled us to identify a few embedded internal shell features, such as the origin of the apex, which is the firmly attached region of the soft tissue connecting the umbilicus to the external morphology. Diffraction-enhanced imaging can provide high-quality images of soft tissues valuable for biology.

  4. Neutron Powder Diffraction Studies of Ca2-xSrxCoWO6 Double Perovskites

    International Nuclear Information System (INIS)

    Zhou, Qingdi; Kennedy, Brendan; Elcombe, Margaret

    2005-01-01

    Full text: A series of double perovskite compounds of A 2-x Sr x CoWO 6 (A = Ca, Ba) were synthesized and the room- and variable-temperature structural phase transitions have been studied by synchrotron and neutron powder diffraction techniques. These studies demonstrated that the symmetry increases as the average size of the A-site cation increases. These transitions are associated with the gradual reduction and ultimately removal of the octahedral tiles of the BO 6 octahedra. Temperature dependent structural studies have been undertaken for selected samples. The transition to cubic is continuous in the three Ca doped samples studied as a function of temperature, Ca 2-x Sr x CoWO 6 x = 1.8, 1.7, 1.6, however in each case analysis of the spontaneous strain shows the transition to be tricritical rather than second order in nature. Where observed the temperature induced P2 1 /n to I4/m transition is first order as required by symmetry. (authors)>>>>

  5. X-ray detectors for diffraction studies and their use with synchrotron radiation

    International Nuclear Information System (INIS)

    Milch, J.

    1976-02-01

    All techniques for X-ray diffraction studies on biological materials exhibit certain limitations. The characteristics of several X-ray detection systems, namely film, multiwire proportional counter and image intensified TV, are discussed and compared for application to specific biological studies. For the high count-rate situation existing at a synchrotron, it is shown that film is a good choice, but that the image intensified TV exhibits significant advantages. The details of such a system now being used at Princeton with a low intensity source are given and current results presented

  6. Non-destructive synchrotron X-ray diffraction mapping of a Roman painting

    International Nuclear Information System (INIS)

    Dooryhee, E.; Anne, M.; Hodeau, J.-L.; Martinetto, P.; Rondot, S.; Bardies, I.; Salomon, J.; Walter, P.; Vaughan, G.B.M.

    2005-01-01

    The history and the properties of materials are deduced not only from their elemental and molecular signatures, but also from their exact phase compositions, and from the structures and the defects of their constituents. Here we implement a non-destructive synchrotron X-ray based method, which combines both the quantitative structural content of diffraction and the imaging mode. As a demonstration case, the pigments of a Roman wall painting are examined. The joined elemental and mineral maps mimic the major features of the painting. Different structural phases made of common atomic elements are differentiated. Textures and graininess are measured and related to the artist's know-how. (orig.)

  7. Neutron powder diffraction and high-pressure synchrotron x-ray diffraction study of tantalum nitrides

    Science.gov (United States)

    Feng, Lei-hao; Hu, Qi-wei; Lei, Li; Fang, Lei-ming; Qi, Lei; Zhang, Lei-lei; Pu, Mei-fang; Kou, Zi-li; Peng, Fang; Chen, Xi-ping; Xia, Yuan-hua; Kojima, Yohei; Ohfuji, Hiroaki; He, Duan-wei; Chen, Bo; Irifune, Tetsuo

    2018-02-01

    Not Available Project supported by the Research Foundation of Key Laboratory of Neutron Physics (Grant No. 2015BB03), the National Natural Science Foundation of China (Grant Nos. 11774247), the Science Foundation for Excellent Youth Scholars of Sichuan University (Grant No. 2015SCU04A04), and the Joint Usage/Research Center PRIUS (Ehime University, Japan) and Chinese Academy of Sciences (Grant No. 2017-BEPC-PT-000568).

  8. Comparison of neutron and synchrotron diffraction measurements of residual stress in bead-on-plate weldments

    International Nuclear Information System (INIS)

    Paradowska, A.M.; Price, J.W.; Finlayson, T.R.; Lienert, U.; Ibrahim, R.

    2010-01-01

    This paper explores the use of neutron and synchrotron diffractions for the evaluation of residual stresses in welded components. It has been shown that it is possible to achieve very good agreement between the two independent diffraction techniques. This study shows the significance of the weld start and end sites on the residual strain/stress distribution. Quantitative evaluation of the residual stress development process for multibead weldments has been presented. Some measurements were also taken before and after postweld stress relieving to establish the reduction and redistribution of the residual stress. The detailed measurements of residual stress around the weld achieved in this work significantly improve the knowledge and understanding of residual stress in welded components.

  9. Powder Handling Device for X-ray Diffraction Analysis with Minimal Sample Preparation, Phase II

    Data.gov (United States)

    National Aeronautics and Space Administration — This project consists in developing a Vibrating Powder Handling System for planetary X-Ray Diffraction instruments. The principle of this novel sample handling...

  10. Structural studies at high pressure using time-of-flight neutron powder diffraction

    International Nuclear Information System (INIS)

    Jorgensen, J.D.

    1989-07-01

    Time-of-flight neutron powder diffraction offers unique capabilities for structural studies at high pressure. Scientific applications have included studies of compression mechanisms, new high-pressure structures, and phase transitions. 11 refs., 1 fig

  11. A note on the limitations of the magnetic axis direction determination by neutron powder diffraction

    International Nuclear Information System (INIS)

    Shaked, Hagai

    2004-01-01

    Rotation crystal symmetry analysis of the magnetic intensities in neutron powder diffraction from magnetically ordered, collinear structures is performed. This analysis, making no reference to a specific crystal system, leads to the well-known limitations on the direction of magnetic axis determination by neutron powder diffraction. It shows that due to the second-order dependence of the magnetic intensity on the magnetic axis components, these limitations result solely from the crystal rotation symmetry in the magnetically ordered state

  12. Probing deformation substructure by synchrotron X-ray diffraction and dislocation dynamics modelling.

    Science.gov (United States)

    Korsunsky, Alexander M; Hofmann, Felix; Song, Xu; Eve, Sophie; Collins, Steve P

    2010-09-01

    Materials characterization at the nano-scale is motivated by the desire to resolve the structural aspects and deformation behavior at length scales relevant to those mechanisms that define the novel and unusual properties of nano-structured materials. A range of novel techniques has recently become accessible with the help of synchrotron X-ray beams that can be focused down to spot sizes of less than a few microns on the sample. The unique combination of tunability (energy selection), parallelism and brightness of synchrotron X-ray beams allows their use for high resolution diffraction (determination of crystal structure and transformations, analysis of dislocation sub-structures, orientation and texture analysis, strain mapping); small angle X-ray scattering (analysis of nano-scale voids and defects; orientation analysis) and imaging (radiography and tomography). After a brief review of the state-of-the-art capabilities for monochromatic and white beam synchrotron diffraction, we consider the usefulness of these techniques for the task of bridging the gap between experiment and modeling. Namely, we discuss how the experiments can be configured to provide information relevant to the validation and improvement of modeling approaches, and also how the results of various simulations can be post-processed to improve the possibility of (more or less) direct comparison with experiments. Using the example of some recent experiments carried out on beamline 116 at Diamond Light Source near Oxford, we discuss how such experimental results can be interpreted in view and in conjunction with numerical deformation models, particularly those incorporating dislocation effects, e.g., finite-element based pseudo-continuum strain gradient formulations, and discrete dislocation simulations. Post-processing of FE and discrete dislocation simulations is described, illustrating the kind of information that can be extracted from comparisons between modeling and experimental data.

  13. Monitoring protein precipitates by in-house X-ray powder diffraction

    DEFF Research Database (Denmark)

    Ståhl, Kenny; Frankær, Christian Grundahl; Petersen, Jakob

    2013-01-01

    Powder diffraction from protein powders using in-house diffractometers is an effective tool for identification and monitoring of protein crystal forms and artifacts. As an alternative to conventional powder diffractometers a single crystal diffractometer equipped with an X-ray micro-source can...... of such calculated powder patterns from insulin and lysozyme have been included in the powder diffraction database and successfully used for search-match identification. However, the fit could be much improved if peak asymmetry and multiple bulk-solvent corrections were included. When including a large number...... of protein data sets in the database some problems can be foreseen due to the large number of overlapping peaks in the low-angle region, and small differences in unit cell parameters between pdb-data and powder data. It is suggested that protein entries are supplied with more searchable keywords as protein...

  14. A synchrotron X-ray diffraction study of non-proportional strain-path effects

    International Nuclear Information System (INIS)

    Collins, D.M.; Erinosho, T.; Dunne, F.P.E.; Todd, R.I.; Connolley, T.; Mostafavi, M.; Kupfer, H.; Wilkinson, A.J.

    2017-01-01

    Common alloys used in sheet form can display a significant ductility benefit when they are subjected to certain multiaxial strain paths. This effect has been studied here for a polycrystalline ferritic steel using a combination of Nakajima bulge testing, X-ray diffraction during biaxial testing of cruciform samples and crystal plasticity finite element (CPFE) modelling. Greatest gains in strain to failure were found when subjecting sheets to uniaxial loading followed by balanced biaxial deformation, resulting in a total deformation close to plane-strain. A combined strain of approximately double that of proportional loading was achieved. The evolution of macrostrain, microstrain and texture during non-proportional loading were evaluated by in-situ high energy synchrotron diffraction. The results have demonstrated that the inhomogeneous strain accumulation from non-proportional deformation is strongly dependent on texture and the applied strain-ratio of the first deformation pass. Experimental diffraction evidence is supported by results produced by a novel method of CPFE-derived diffraction simulation. Using constitutive laws selected on the basis of good agreement with measured lattice strain development, the CPFE model demonstrated the capability to replicate ductility gains measured experimentally.

  15. Synchrotron Diffraction Studies of Spontaneous Magnetostriction in Rare Earth Transition Metal Compounds

    Energy Technology Data Exchange (ETDEWEB)

    Yang, Ning [Iowa State Univ., Ames, IA (United States)

    2004-12-19

    Thermal expansion anomalies of R2Fe14B and R2Fe17Cx (x = 0,2) (R = Y, Nd, Gd, Tb, Er) stoichiometric compounds are studied with high-energy synchrotron X-ray powder diffraction using Debye-Schemer geometry in temperature range 10K to 1000K. Large spontaneous magnetostriction up to their Curie temperatures (Tc) is observed. The a-axes show relatively larger invar effects than c-axes in the R2Fe14B compounds whereas the R2Fe17Cx show the contrary anisotropies. The iron sub-lattice is shown to dominate the spontaneous magnetostriction of the compounds. The contribution of the rare earth sublattice is roughly proportional to the spin magnetic moment of the rare earth in the R2Fe14B compounds but in R2Fe17Cx, the rare earth sub-lattice contribution appears more likely to be dominated by the local bonding. The calculation of spontaneous magnetostrain of bonds shows that the bonds associated with Fe(j2) sites in R2Fe14B and the dumbbell sites in R2Fe17Cx have larger values, which is strongly related to their largest magnetic moment and Wigner-Seitz atomic cell volume. The roles of the carbon atoms in increasing the Curie temperatures of the R2Fe17 compounds are attributed to the increased separation of Fe hexagons. The R2Fe17 and R2Fe14B phases with magnetic rare earth ions also show anisotropies of thermal expansion above c. For R2Fe17 and R2Fe14B the a a/a c > 1 whereas the anisotropy is reversed with the interstitial carbon in R2Fe17. The average bond magnetostrain is shown to be a possible predictor of the magnetic moment of Fe sites in the compounds. Both of the theoretical and

  16. A flow cell for the study of gas-solid reactions via in situ powder X-ray diffraction

    Science.gov (United States)

    Scarlett, Nicola V. Y.; Hewish, Damien; Pattel, Rachel; Webster, Nathan A. S.

    2017-10-01

    This paper describes the development and testing of a novel capillary flow cell for use in in situ powder X-ray diffraction experiments. It is designed such that it achieves 200° of rotation of the capillary whilst still allowing the flow of gas through the sample and the monitoring of off gas via mass spectrometry, gas chromatography, or other such analytical techniques. This high degree of rotation provides more uniform heating of the sample than can be achieved in static cells or those with lower rotational ranges and consequently also improves particle statistics. The increased uniformity of heating provides more accurate temperature calibration of the experimental setup as well. The cell is designed to be held in a standard goniometer head and is therefore suitable for use in many laboratory and synchrotron instruments.

  17. Experimental and theoretical aspects of ab initio structure determination using powder diffraction techniques

    International Nuclear Information System (INIS)

    David, W.I.F.; Johnson, M.W.; Wilson, C.C.

    1988-01-01

    Neutron powder diffraction has, over the past two decades, developed into a powerful technique for the refinement of moderately complex crystal structures. The advent of a new generation of ultra-high resolution X-ray and neutron powder diffractometers, however, not only permits the refinement of more complex materials but also opens up new areas of research. Perhaps the most exciting development in powder diffraction techniques associated with high resolution is the ab initio determination of crystal structures. This has until recently been possible, in a routine way, only by single crystal studies. The compression of three dimensions of diffraction data to the one dimension of a powder diffraction pattern leads to an unavoidable loss of information. For many, but not all, crystal symmetries high resolution minimises this loss thus allowing the intensities of a sufficient number of resolved Bragg reflections from moderately complex materials to be extracted for use in structure solution by direct methods of phase determination and by Patterson methods. Recent structure determination using the high resolution powder diffractometer, HRPD, at ISIS will be presented. The inherent limitations resulting from crystal and instrumental resolution are discussed along with maximum entropy techniques that seek to optimise the information content of a powder diffraction pattern. (author) 36 refs., 1 fig., 3 tabs

  18. X-ray diffraction applied to powder studies

    International Nuclear Information System (INIS)

    Assaf, Josiane

    1982-01-01

    the thesis starts with general definitions of x-ray: their nature, sources and production mechanism. it describesdifferent methods such as Debye-scherrer, absorption coefficient method, diffractometer method...The use of pattern-fitting techniques for the characterization of the microstructure is discussed through applications to nanocrystalline materials. Remarkable results achieved in the solution of crystal structures are presented, as well as the impact in solid-state chemistry of powder crystallography, particularly for elucidating the crystal chemistry of families of compounds for which only powders are available

  19. The materials science synchrotron beamline EDDI for energy-dispersive diffraction analysis

    International Nuclear Information System (INIS)

    Genzel, Ch.; Denks, I.A.; Gibmeier, J.; Klaus, M.; Wagener, G.

    2007-01-01

    In April 2005 the materials science beamline EDDI (Energy Dispersive DIffraction) at the Berlin synchrotron storage ring BESSY started operation. The beamline is operated in the energy-dispersive mode of diffraction using the high energy white photon beam provided by a superconducting 7 T multipole wiggler. Starting from basic information on the beamline set-up, its measuring facilities and data processing concept, the wide range of applications for energy-dispersive diffraction is demonstrated by a series of examples coming from different fields in materials sciences. It will be shown, that the EDDI beamline is especially suitable for the investigation of structural properties and gradients in the near surface region of polycrystalline materials. In particular, this concerns the analysis of multiaxial residual stress fields in the highly stressed surface zone of technical parts. The high photon flux further facilitates fast in situ experiments at room as well as high temperature to monitor for example the growth kinetics and reaction in thin film growth

  20. Synchrotron hard X-ray imaging of shock-compressed metal powders

    Science.gov (United States)

    Rutherford, Michael E.; Chapman, David J.; Collinson, Mark A.; Jones, David R.; Music, Jasmina; Stafford, Samuel J. P.; Tear, Gareth R.; White, Thomas G.; Winters, John B. R.; Drakopoulos, Michael; Eakins, Daniel E.

    2015-06-01

    This poster will present the application of a new, high-energy (50 to 250 keV) synchrotron X-ray radiography technique to the study of shock-compressed granular materials. Following plate-impact loading, transmission radiography was used to quantitatively observe the compaction and release processes in a range of high-Z metal powders (e.g. Fe, Ni, Cu). By comparing the predictions of 3D numerical models initialized from X-ray tomograms-captured prior to loading-with experimental results, this research represents a new approach to refining mesoscopic compaction models. The authors gratefully acknowledge the ongoing support of Imperial College London, EPSRC, STFC and the Diamond Light Source, and AWE Plc.

  1. Source assemblage types for cratonic diamonds from X-ray synchrotron diffraction

    Science.gov (United States)

    Nestola, F.; Alvaro, M.; Casati, M. N.; Wilhelm, H.; Kleppe, A. K.; Jephcoat, A. P.; Domeneghetti, M. C.; Harris, J. W.

    2016-11-01

    Three single crystals of clinopyroxene trapped within three different gem-quality diamonds from the Udachnaya kimberlite (Siberia, Russia) were analysed in situ by single-crystal synchrotron X-ray diffraction in order to obtain information on their chemical composition and infer source assemblage type. A non-destructive approach was used with high-energy (≈ 60 keV; λ ≈ 0.206 Å) at I15, the extreme-conditions beamline at Diamond Light Source. A dedicated protocol was used to center the mineral inclusions located deep inside the diamonds in the X-ray beam. Our results reveal that two of the inclusions can be associated with peridotitic paragenesis whereas the third is eclogitic. This study also demonstrates that this non-destructive experimental approach is extremely efficient in evaluating the origin of minerals trapped in their diamond hosts.

  2. Structural Investigation of Sodium Layered Oxides Via in Situ Synchrotron X-Ray Diffraction

    DEFF Research Database (Denmark)

    Jung, Young Hwa; Christiansen, Ane Sælland; Johnsen, Rune

    2015-01-01

    Sodium layered oxides with mixed transition metals have received significant attention as positive electrode candidates for sodium-ion batteries due to high reversible capacity. Sodium layered oxides would be more promising candidates than lithium-compounds in terms of high stability of MO2 slabs...... after extraction of Na induced from larger ionic size of Na. In addition, rich crystal chemistry for sodium layered compounds is available since larger Na+ ion is stable in more spacious prismatic site as compared to Li+ ion. In view of this, the phase transformation of layered compounds during......-situ synchrotron XRD experiments. A capillary Na-based cell is designed to minimize interference in other substances such as a separator or external battery parts. This approach could give us to obtain clear diffraction patterns with high intensity during electrochemical reaction in a short period of time without...

  3. Ab initio structure determination via powder X-ray diffraction

    Indian Academy of Sciences (India)

    Unknown

    A46 297. 28. Sinclair D C, Watson C J, Howie R A, Skakle J M S, Coats A M, Kirk C A, Lachowski E E and Marr J 1998 J. Mater. Chem. 8 281. 29. Sinclair D C, Marinou E and Skakle J M S 1999 J. Mater. Chem. 9 2617. 30. Shirley R 1999 The CRYSFIRE system for automatic powder indexing: User's manual. (Lattice Press)

  4. The T2 phase in the Nb–Si–B system studied by ab initio calculations and synchrotron X-ray diffraction

    International Nuclear Information System (INIS)

    Joubert, J.-M.; Colinet, C.; Rodrigues, G.; Suzuki, P.A.; Nunes, C.A.; Coelho, G.C.; Tedenac, J.-C.

    2012-01-01

    The solid solution based on Nb 5 Si 3 (Cr 5 B 3 structure type, D8 l , tI32, I4/mcm, No140, a=6.5767 Å, c=11.8967 Å) in the Nb–Si–B system was studied from the structural and thermodynamic point of view both experimentally and by ab initio calculations. Rietveld refinement of powder X-ray synchrotron data allowed to determine the boron to silicon substitution mechanism and the structural parameters. Ab initio calculations of different ordered compounds and selected disordered alloys allowed to obtain in addition to the enthalpy of formation of the solution, substitution mechanism and structural parameters which are in excellent agreement with the experimental data. The stability of the phase is discussed. - Graphial abstract: Valence-charge electron localization function in the z=0 plane of the D8 l structure for the ordered compound Nb 5 SiB 2 . Highlights: ► Coupling between ab initio data and experimental results from synchrotron powder diffraction. ► Excellent agreement between the two techniques for the site occupancies and internal coordinates. ► Explanation of the phase stability up to Nb 5 SiB 2 .

  5. In situ Investigation of Titanium Powder Microwave Sintering by Synchrotron Radiation Computed Tomography

    Directory of Open Access Journals (Sweden)

    Yu Xiao

    2016-01-01

    Full Text Available In this study, synchrotron radiation computed tomography was applied to investigate the mechanisms of titanium powder microwave sintering in situ. On the basis of reconstructed images, we observed that the sintering described in this study differs from conventional sintering in terms of particle smoothing, rounding, and short-term growth. Contacted particles were also isolated. The kinetic curves of sintering neck growth and particle surface area were obtained and compared with those of other microwave-sintered metals to examine the interaction mechanisms between mass and microwave fields. Results show that sintering neck growth accelerated from the intermediate period; however, this finding is inconsistent with that of aluminum powder microwave sintering described in previous work. The free surface areas of the particles were also quantitatively analyzed. In addition to the eddy current loss in metal particles, other heating mechanisms, including dielectric loss, interfacial polarization effect, and local plasma-activated sintering, contributed to sintering neck growth. Thermal and non-thermal effects possibly accelerated the sintering neck growth of titanium. This study provides a useful reference of further research on interaction mechanisms between mass and microwave fields during microwave sintering.

  6. Application of synchrotron radiation to analyze the precipitation in ODS materials before irradiation in Fe-9%Cr single grain of powder and consolidated Fe-18%Cr

    Energy Technology Data Exchange (ETDEWEB)

    Bechade, J.-L., E-mail: jean-luc.bechade@cea.fr [CEA, DEN, Service de Recherches Metallurgiques Appliquees, 91191 Gif-sur-Yvette (France); Menut, D., E-mail: denis.menut@cea.fr [CEA, DEN, Service de Recherches Metallurgiques Appliquees, 91191 Gif-sur-Yvette (France); Lescoat, M.-L., E-mail: marie-laure.lescoat@cea.fr [CEA, DEN, Service de Recherches Metallurgiques Appliquees, 91191 Gif-sur-Yvette (France); Sitaud, B., E-mail: bruno.sitaud@synchrotron-soleil.fr [Synchrotron SOLEIL, Division Experiences, Ligne de MARS, L' Orme des Merisiers, Saint Aubin BP48, 91 192 Gif-sur-Yvette Cedex (France); Schlutig, S., E-mail: sandrine.schlutig@synchrotron-soleil.fr [Synchrotron SOLEIL, Division Experiences, Ligne de MARS, L' Orme des Merisiers, Saint Aubin BP48, 91 192 Gif-sur-Yvette Cedex (France); Solari, P.L., E-mail: pier-lorenzo.solari@synchrotron-soleil.fr [Synchrotron SOLEIL, Division Experiences, Ligne de MARS, L' Orme des Merisiers, Saint Aubin BP48, 91 192 Gif-sur-Yvette Cedex (France); Llorens, I., E-mail: isabelle.llorens@synchrotron-soleil.fr [Synchrotron SOLEIL, Division Experiences, Ligne de MARS, L' Orme des Merisiers, Saint Aubin BP48, 91 192 Gif-sur-Yvette Cedex (France); Hermange, H., E-mail: herve.hermange@synchrotron-soleil.fr [Synchrotron SOLEIL, Division Experiences, Ligne de MARS, L' Orme des Merisiers, Saint Aubin BP48, 91 192 Gif-sur-Yvette Cedex (France); and others

    2012-09-15

    Oxide Dispersion Strengthened (ODS) materials are candidates for structural components of GEN IV and fusion reactors. These materials are reinforced by nano-oxides (size of the smallest <3 nm) and the excellent mechanical properties obtained with such materials have to be kept in service. The aim of this paper is to present the capabilities of the synchrotron radiation to finely characterize the dispersion of second phases in ODS steels (Fe-9%Cr single grain of powder and consolidated Fe-18%Cr) and to study the precipitation mechanisms. This paper illustrates the results from first analyses performed on various unirradiated ODS steels elaborated at CEA using X-ray diffraction (XRD) and X-ray absorption spectroscopy (XAS) at the Multi-Analysis on Radioactive Sample (MARS) beamline of the SOLEIL synchrotron facility. The complementarities of both techniques, XRD and XAS, especially well appropriated to structural and local environment analyses for nano particles are presented. Results obtained with synchrotron radiation are also enriched by comparison with Transmission Electron Microscopy (TEM) observations performed on similar samples.

  7. X-ray diffraction microstructural analysis of bimodal size distribution MgO nano powder

    International Nuclear Information System (INIS)

    Suminar Pratapa; Budi Hartono

    2009-01-01

    Investigation on the characteristics of x-ray diffraction data for MgO powdered mixture of nano and sub-nano particles has been carried out to reveal the crystallite-size-related microstructural information. The MgO powders were prepared by co-precipitation method followed by heat treatment at 500 degree Celsius and 1200 degree Celsius for 1 hour, being the difference in the temperature was to obtain two powders with distinct crystallite size and size-distribution. The powders were then blended in air to give the presumably bimodal-size- distribution MgO nano powder. High-quality laboratory X-ray diffraction data for the powders were collected and then analysed using Rietveld-based MAUD software using the lognormal size distribution. Results show that the single-mode powders exhibit spherical crystallite size (R) of 20(1) nm and 160(1) nm for the 500 degree Celsius and 1200 degree Celsius data respectively with the nano metric powder displays narrower crystallite size distribution character, indicated by lognormal dispersion parameter of 0.21 as compared to 0.01 for the sub-nano metric powder. The mixture exhibits relatively more asymmetric peak broadening. Analysing the x-ray diffraction data for the latter specimen using single phase approach give unrealistic results. Introducing two phase models for the double-phase mixture to accommodate the bimodal-size-distribution characteristics give R = 100(6) and σ = 0.62 for the nano metric phase and R = 170(5) and σ= 0.12 for the σ sub-nano metric phase. (author)

  8. Energy dispersive x-ray diffraction from Ge, GaAs, GaP, and AlSb at high pressures using synchrotron radiation

    International Nuclear Information System (INIS)

    Baublitz, M.A. Jr.

    1982-01-01

    The practicality of energy dispersive X-ray diffraction from high pressure powder specimens using synchrotron radiation has been demonstrated. Reasonable quantitative agreement has been obtained between the experimental diffraction data and the theoretical relative integrated intensities of the diffraction lines for known structures under rather hydrostatic pressure conditions. Pressure-induced structural phase transitions in Ge, GaAs, GaP, and AlSb have been studied in some detail with this energy dispersive diffraction method. Ge transforms to the beta-Sn tetragonal structure as previously observed by Jamieson, but the transition pressure is 80 +- 5 kbars, a somewhat lower value than generally reported. GaAs exhibits an orthorhombic structure above 172 +- 7 kbars, GaP a tetragonal structure above 215 +- 8 kbars, and AlSb an orthorhombic structure above 77 +- 5 kbars. Although the space groups of these latter three high pressure polymorphs have not been determined unequivocally, mainly due to the apparent presence of crystalline defects, some possible models are described for these high pressure structures. Lastly, a comparison of the existing phase transition data with the theoretical diagrams of Zunger, based on pseudopotential length scales, indicates that it may be possible to predict the high pressure polymorphs of crystals with diamond or cubic zincblende structures at ambient conditions

  9. Powder diffraction on a long-pulse spallation source

    International Nuclear Information System (INIS)

    Stride, J.A.; Wechsler, D.; Mezei, F.; Bleif, H.-J.

    2000-01-01

    Monte Carlo simulations have been performed for a time-of-flight monochromator powder diffractometer housed on a thermal moderator at a Long-Pulse Spallation Source and for a conventional crystal monochromator instrument on a thermal moderator of a reactor source of four times the time-averaged flux. By designing the time-of-flight instrument to utilise the inherent advantages of the technique whilst optimising to the peak performance of the crystal monochromator case, the performance of the TOF-instrument is shown to exceed that of the reactor-based diffractometer, despite the lower time-averaged flux of the source. Further, a simple extrapolation of the results obtained for the pulsed-source shows that such a TOF diffractometer would out-perform a conventional instrument if both were to be housed on the same reactor

  10. The MYTHEN detector for X-ray powder diffraction experiments at the Swiss Light Source

    International Nuclear Information System (INIS)

    Bergamaschi, Anna; Cervellino, Antonio; Dinapoli, Roberto; Gozzo, Fabia; Henrich, Beat; Johnson, Ian; Kraft, Philipp; Mozzanica, Aldo; Schmitt, Bernd; Shi, Xintian

    2010-01-01

    A report on the characterization, calibration and performances of the MYTHEN photon-counting silicon microstrip detector at the powder diffraction station at the Swiss Light Source is given. The MYTHEN single-photon-counting silicon microstrip detector has been developed at the Swiss Light Source for time-resolved powder diffraction experiments. An upgraded version of the detector has been installed at the SLS powder diffraction station allowing the acquisition of diffraction patterns over 120° in 2θ in fractions of seconds. Thanks to the outstanding performance of the detector and to the calibration procedures developed, the quality of the data obtained is now comparable with that of traditional high-resolution point detectors in terms of FWHM resolution and peak profile shape, with the additional advantage of fast and simultaneous acquisition of the full diffraction pattern. MYTHEN is therefore optimal for time-resolved or dose-critical measurements. The characteristics of the MYTHEN detector together with the calibration procedures implemented for the optimization of the data are described in detail. The refinements of two known standard powders are discussed together with a remarkable application of MYTHEN to organic compounds in relation to the problem of radiation damage

  11. Digital Image Correlation of 2D X-ray Powder Diffraction Data for Lattice Strain Evaluation

    Directory of Open Access Journals (Sweden)

    Hongjia Zhang

    2018-03-01

    Full Text Available High energy 2D X-ray powder diffraction experiments are widely used for lattice strain measurement. The 2D to 1D conversion of diffraction patterns is a necessary step used to prepare the data for full pattern refinement, but is inefficient when only peak centre position information is required for lattice strain evaluation. The multi-step conversion process is likely to lead to increased errors associated with the ‘caking’ (radial binning or fitting procedures. A new method is proposed here that relies on direct Digital Image Correlation analysis of 2D X-ray powder diffraction patterns (XRD-DIC, for short. As an example of using XRD-DIC, residual strain values along the central line in a Mg AZ31B alloy bar after 3-point bending are calculated by using both XRD-DIC and the conventional ‘caking’ with fitting procedures. Comparison of the results for strain values in different azimuthal angles demonstrates excellent agreement between the two methods. The principal strains and directions are calculated using multiple direction strain data, leading to full in-plane strain evaluation. It is therefore concluded that XRD-DIC provides a reliable and robust method for strain evaluation from 2D powder diffraction data. The XRD-DIC approach simplifies the analysis process by skipping 2D to 1D conversion, and opens new possibilities for robust 2D powder diffraction data analysis for full in-plane strain evaluation.

  12. In situ analysis of cracks in structural materials using synchrotron X-ray tomography and diffraction

    International Nuclear Information System (INIS)

    Steuwer, A.; Edwards, L.; Pratihar, S.; Ganguly, S.; Peel, M.; Fitzpatrick, M.E.; Marrow, T.J.; Withers, P.J.; Sinclair, I.; Singh, K.D.; Gao, N.; Buslaps, T.; Buffiere, J.-Y.

    2006-01-01

    The structural integrity and performance of many components and structures are dominated by cracks and hence the study of cracked bodies study is of major economical and social importance. Despite nearly 30 years of study, there is still no detailed consensus regarding either the fundamental parameters that drive cracks or the precise mechanisms of their growth in most materials. Thus, virtually all crack life prediction models currently in engineering use are largely phenomenological rather than physically based. Historically, a major hindrance to our understanding of crack initiation and propagation has been the inability to measure either the crack tip stresses or the crack morphology deep within materials. The development of very high-resolution strain and tomography mapping on third generation synchrotron sources such as the ESRF has opened up the possibility of developing complementary techniques to monitor the entire plastic/process zone growth mechanisms and the accompanying crack tip field and crack wake field around growing cracks. If realized, such techniques would produce unique information that would be invaluable both in validating present finite element simulations of fatigue crack growth and in developing the future high accuracy simulations necessary for the development of physically realistic fatigue life-prediction models. Recent technique developments at the ESRF, Grenoble, opens up the possibility of imaging cracks and crack tip stress/strain fields, and the ability to study the extend of crack closure and overload effects, even under in situ loading. In this paper, first results from synchrotron X-ray diffraction and tomography experiments performed on ID11 and ID19 (respectively) at the ESRF, Grenoble, are presented and discussed in comparison with predictions from finite element modeling

  13. Qualitative analysis of powder x-ray diffraction data

    International Nuclear Information System (INIS)

    Raftery, T.

    1999-01-01

    Full text: The main task of qualitative analysis is the determination of the presence of major, minor and if practical trace phases in a sample. The attainment of this goal is dependent on the quality of alignment (line position and intensity) as well as quality of sample preparation. Identification is generally on the basis of structure and dependent on the use of reference patterns. There are inherent limitations to the use of reference patterns including lack of reference patterns for the phase of interest (rare), solid solutions or substitutions (likely) and poor quality of reference patterns (unusual). With multiphase samples, there are the added problems of line overlap or interference, determining minor or trace phases in the presence of major phases, the decrease of intensity with concentration and influence of mass absorption on intensities. Within multiphase samples there may be many phases, some of which are in low abundance. It is sometimes possible (and usually desirable) to fractionate the sample by some physical or chemical method (while attempting not to create new phases as a result). It is usually important and often critical to have available supplementary information about the sample - either chemical or physical, or a history of preparation or formation. A central issue is what constitutes a match. A match is an adequate accounting of the distribution of intensity in the diffraction pattern. The match can be thought of in terms of a sum of δ2θ (or δd/d) and/or δI/I ref , and the consistency with known information. The calculated measures give rise to the figures of merit (FOM) of search match programs. It must always be remembered that two compounds of the same space group and similar cell parameters (eg. FCC metals) are going to have very similar diffraction patterns - any search/match technique usually arrives at a stage where there is a list of possibilities that must be decided between. The range search-match techniques span manual

  14. Characterization of Gas-Solid Reactions using In Situ Powder X-ray Diffraction

    DEFF Research Database (Denmark)

    Møller, Kasper Trans; Hansen, Bjarne Rosenlund Søndertoft; Dippel, Ann-Christin

    2014-01-01

    X-ray diffraction is a superior technique for structural characterization of crystalline matter. Here we review the use of in situ powder X-ray diffraction (PXD) mainly for real-time studies of solid/gas reactions, data analysis and the extraction of valuable knowledge of structural, chemical...... by diffraction techniques, e.g. crystallite size. The aim of this review is to provide new inspiration for utilization of in situ PXD for characterization of a wide range of properties beyond the scope of crystal structure solution....

  15. A cubic-anvil high-pressure device for pulsed neutron powder diffraction.

    Science.gov (United States)

    Abe, J; Arakawa, M; Hattori, T; Arima, H; Kagi, H; Komatsu, K; Sano-Furukawa, A; Uwatoko, Y; Matsubayashi, K; Harjo, S; Moriai, A; Ito, T; Aizawa, K; Arai, M; Utsumi, W

    2010-04-01

    A compact cubic-anvil high-pressure device was developed for in situ neutron powder diffraction studies. In this device, a cubic shaped pressure medium is compressed by six anvils, and neutron beams pass through gaps between the anvils. The first high-pressure experiment using this device was conducted at J-PARC and clearly showed the neutron diffraction patterns of Pb. Combining the cubic-anvil high-pressure device with a pulsed neutron source will prove to be a useful tool for neutron diffraction experiments.

  16. Incident spectrum determination for time-of-flight neutron powder diffraction data analysis

    International Nuclear Information System (INIS)

    Hodges, J. P.

    1998-01-01

    Accurate characterization of the incident neutron spectrum is an important requirement for precise Rietveld analysis of time-of-flight powder neutron diffraction data. Without an accurate incident spectrum the calculated model for the measured relative intensities of individual Bragg reflections will possess systematic errors. We describe a method for obtaining an accurate numerical incident spectrum using data from a transmitted beam monitor

  17. Proceedings of the 1986 workshop on advanced time-of-flight neutron powder diffraction

    Energy Technology Data Exchange (ETDEWEB)

    Lawson, A.C.; Smith, K. (comps.)

    1986-09-01

    This report contains abstracts of talks and summaries of discussions from a small workshop held to discuss the future of time-of-flight neutron powder diffraction and its implementation at the Los Alamos Neutron Scattering Center. 47 refs., 3 figs.

  18. Proceedings of the 1986 workshop on advanced time-of-flight neutron powder diffraction

    International Nuclear Information System (INIS)

    Lawson, A.C.; Smith, K.

    1986-09-01

    This report contains abstracts of talks and summaries of discussions from a small workshop held to discuss the future of time-of-flight neutron powder diffraction and its implementation at the Los Alamos Neutron Scattering Center. 47 refs., 3 figs

  19. Crystal structure determination from powder diffraction data of the coumarin vanillin chalcone

    Czech Academy of Sciences Publication Activity Database

    Ghouili, A.; Rohlíček, Jan; Ayed, T.B.; Hassen, R.B.

    2014-01-01

    Roč. 29, č. 4 (2014), s. 361-365 ISSN 0885-7156 Grant - others:AV ČR(CZ) Praemium Academiae Institutional support: RVO:68378271 Keywords : chalcone * absorption spectra * powder diffraction * crystal structure determination * coumarin derivatives Subject RIV: BM - Solid Matter Physics ; Magnetism Impact factor: 0.636, year: 2014

  20. Charge flipping combined with histogram matching to solve complex crystal structures from powder diffraction data

    Czech Academy of Sciences Publication Activity Database

    Baerlocher, Ch.; McCusker, L.B.; Palatinus, Lukáš

    2007-01-01

    Roč. 222, - (2007), s. 47-53 ISSN 0044-2968 Institutional research plan: CEZ:AV0Z10100521 Keywords : charge flipping * histogram-matching * polycrystalline materials * powder diffraction structure analysis Subject RIV: BM - Solid Matter Physics ; Magnetism Impact factor: 1.338, year: 2007

  1. Dihydroxycoumarin Schiff base synthesis and structure determination from powder diffraction data

    Czech Academy of Sciences Publication Activity Database

    Rohlíček, Jan; Ketata, I.; Ben Ayed, T.; Ben Hassen, R.

    2013-01-01

    Roč. 1051, NOV (2013), s. 280-284 ISSN 0022-2860 Grant - others:AV ČR(CZ) AP0701 Program:Akademická prémie - Praemium Academiae Institutional support: RVO:68378271 Keywords : powder diffraction * structure solution * Schiff base * dihydroxycoumarine Subject RIV: BM - Solid Matter Physics ; Magnetism Impact factor: 1.599, year: 2013

  2. In situ neutron powder diffraction and structure determination in controlled humidities.

    Science.gov (United States)

    Ting, Valeska P; Henry, Paul F; Schmidtmann, Marc; Wilson, Chick C; Weller, Mark T

    2009-12-28

    A controlled-humidity sample environment has been constructed, allowing bulk powder samples undergoing humidity-induced phase transitions and reactions to be studied via in situ neutron diffraction. Associated developments in data collection and analysis permit this to be achieved without the use of D(2)O.

  3. Application of the ellipsoid modeling of the average shape of nanosized crystallites in powder diffraction

    DEFF Research Database (Denmark)

    Katerinopoulou, Anna; Balic Zunic, Tonci; Lundegaard, Lars Fahl

    2012-01-01

    Anisotropic broadening correction in X-ray powder diffraction by an ellipsoidal formula is applied on samples with nanosized crystals. Two cases of minerals with largely anisotropic crystallite shapes are presented. The properly applied formalism not only improves the fitting of the theoretical...

  4. Soft x-ray resonant magnetic powder diffraction on PrNiO{sub 3}

    Energy Technology Data Exchange (ETDEWEB)

    Staub, U [Swiss Light Source, Paul Scherrer Institut, CH-5232 Villigen PSI (Switzerland); GarcIa-Fernandez, M [Swiss Light Source, Paul Scherrer Institut, CH-5232 Villigen PSI (Switzerland); Mulders, A M [Department of Applied Physics, Curtin University of Technology, GPO Box U1987, Perth WA 6845 (Australia); Bodenthin, Y [Swiss Light Source, Paul Scherrer Institut, CH-5232 Villigen PSI (Switzerland); MartInez-Lope, M J [Instituto de Ciencia de Materiales de Madrid, CSIC, Cantoblanco, E-28049 Madrid (Spain); Alonso, J A [Instituto de Ciencia de Materiales de Madrid, CSIC, Cantoblanco, E-28049 Madrid (Spain)

    2007-03-07

    We report on the first soft x-ray resonant powder diffraction experiments performed at the Ni L{sub 2,3} edges of PrNiO{sub 3}. The temperature, polarization and energy dependence of the (1/2 0 1/2) reflection indicates a magnetic origin for the signal. This experiment demonstrates that x-ray resonant magnetic powder diffraction can be relatively easily performed in the soft x-ray regime due to the very large enhancement factors at the absorption edges. Such experiments allow us to extract important information on the electronic states of the d shell. Similar results can be anticipated from orbital reflections measured in a powder. (fast track communication)

  5. Classification of lead white pigments using synchrotron radiation micro X-ray diffraction

    Science.gov (United States)

    Welcomme, E.; Walter, P.; Bleuet, P.; Hodeau, J.-L.; Dooryhee, E.; Martinetto, P.; Menu, M.

    2007-12-01

    Lead white pigment was used and synthesised for cosmetic and artistic purposes since the antiquity. Ancient texts describe the various recipes, and preparation processes as well as locations of production. In this study, we describe the results achieved on several paint samples taken from Matthias Grünewald’s works. Grünewald, who was active between 1503 and 1524, was a major painter at the beginning of the German Renaissance. Thanks to X-ray diffraction analysis using synchrotron radiation, it is possible to associate the composition of the paint samples with the masters ancient recipes. Different approaches were used, in reflection and transmission modes, directly on minute samples or on paint cross-sections embedded in resin. Characterisation of lead white pigments reveals variations in terms of composition, graininess and proportion of mineral phases. The present work enlightens the presence of lead white as differentiable main composition groups, which could be specific of a period, a know-how or a geographical origin. In this way, we aim at understanding the choices and the trading of pigments used to realise paintings during northern European Renaissance.

  6. Classification of lead white pigments using synchrotron radiation micro X-ray diffraction

    Energy Technology Data Exchange (ETDEWEB)

    Welcomme, E.; Walter, P.; Menu, M. [Centre de Recherche et de Restauration des Musees de France - CNRS UMR 171, Paris (France); Bleuet, P. [European Synchrotron Radiation Facility, BP 220, Grenoble Cedex (France); Hodeau, J.L.; Dooryhee, E.; Martinetto, P. [Institut Neel CNRS-UPR 503-1, 25, Av. des Martyrs, BP 166, Grenoble Cedex 9 (France)

    2007-12-15

    Lead white pigment was used and synthesised for cosmetic and artistic purposes since the antiquity. Ancient texts describe the various recipes, and preparation processes as well as locations of production. In this study, we describe the results achieved on several paint samples taken from Matthias Gruenewald's works. Gruenewald, who was active between 1503 and 1524, was a major painter at the beginning of the German Renaissance. Thanks to X-ray diffraction analysis using synchrotron radiation, it is possible to associate the composition of the paint samples with the masters ancient recipes. Different approaches were used, in reflection and transmission modes, directly on minute samples or on paint cross-sections embedded in resin. Characterisation of lead white pigments reveals variations in terms of composition, graininess and proportion of mineral phases. The present work enlightens the presence of lead white as differentiable main composition groups, which could be specific of a period, a know-how or a geographical origin. In this way, we aim at understanding the choices and the trading of pigments used to realise paintings during northern European Renaissance. (orig.)

  7. Deformation in Metallic Glasses Studied by Synchrotron X-Ray Diffraction

    Directory of Open Access Journals (Sweden)

    Takeshi Egami

    2016-01-01

    Full Text Available High mechanical strength is one of the superior properties of metallic glasses which render them promising as a structural material. However, understanding the process of mechanical deformation in strongly disordered matter, such as metallic glass, is exceedingly difficult because even an effort to describe the structure qualitatively is hampered by the absence of crystalline periodicity. In spite of such challenges, we demonstrate that high-energy synchrotron X-ray diffraction measurement under stress, using a two-dimensional detector coupled with the anisotropic pair-density function (PDF analysis, has greatly facilitated the effort of unraveling complex atomic rearrangements involved in the elastic, anelastic, and plastic deformation of metallic glasses. Even though PDF only provides information on the correlation between two atoms and not on many-body correlations, which are often necessary in elucidating various properties, by using stress as means of exciting the system we can garner rich information on the nature of the atomic structure and local atomic rearrangements during deformation in glasses.

  8. Classification of lead white pigments using synchrotron radiation micro X-ray diffraction

    International Nuclear Information System (INIS)

    Welcomme, E.; Walter, P.; Menu, M.; Bleuet, P.; Hodeau, J.L.; Dooryhee, E.; Martinetto, P.

    2007-01-01

    Lead white pigment was used and synthesised for cosmetic and artistic purposes since the antiquity. Ancient texts describe the various recipes, and preparation processes as well as locations of production. In this study, we describe the results achieved on several paint samples taken from Matthias Gruenewald's works. Gruenewald, who was active between 1503 and 1524, was a major painter at the beginning of the German Renaissance. Thanks to X-ray diffraction analysis using synchrotron radiation, it is possible to associate the composition of the paint samples with the masters ancient recipes. Different approaches were used, in reflection and transmission modes, directly on minute samples or on paint cross-sections embedded in resin. Characterisation of lead white pigments reveals variations in terms of composition, graininess and proportion of mineral phases. The present work enlightens the presence of lead white as differentiable main composition groups, which could be specific of a period, a know-how or a geographical origin. In this way, we aim at understanding the choices and the trading of pigments used to realise paintings during northern European Renaissance. (orig.)

  9. Three-dimensional electron diffraction as a complementary technique to powder X-ray diffraction for phase identification and structure solution of powders

    Directory of Open Access Journals (Sweden)

    Yifeng Yun

    2015-03-01

    Full Text Available Phase identification and structure determination are important and widely used techniques in chemistry, physics and materials science. Recently, two methods for automated three-dimensional electron diffraction (ED data collection, namely automated diffraction tomography (ADT and rotation electron diffraction (RED, have been developed. Compared with X-ray diffraction (XRD and two-dimensional zonal ED, three-dimensional ED methods have many advantages in identifying phases and determining unknown structures. Almost complete three-dimensional ED data can be collected using the ADT and RED methods. Since each ED pattern is usually measured off the zone axes by three-dimensional ED methods, dynamic effects are much reduced compared with zonal ED patterns. Data collection is easy and fast, and can start at any arbitrary orientation of the crystal, which facilitates automation. Three-dimensional ED is a powerful technique for structure identification and structure solution from individual nano- or micron-sized particles, while powder X-ray diffraction (PXRD provides information from all phases present in a sample. ED suffers from dynamic scattering, while PXRD data are kinematic. Three-dimensional ED methods and PXRD are complementary and their combinations are promising for studying multiphase samples and complicated crystal structures. Here, two three-dimensional ED methods, ADT and RED, are described. Examples are given of combinations of three-dimensional ED methods and PXRD for phase identification and structure determination over a large number of different materials, from Ni–Se–O–Cl crystals, zeolites, germanates, metal–organic frameworks and organic compounds to intermetallics with modulated structures. It is shown that three-dimensional ED is now as feasible as X-ray diffraction for phase identification and structure solution, but still needs further development in order to be as accurate as X-ray diffraction. It is expected that three

  10. Kinetic Analyses of Cation Exchange Rates in Synthetic Birnessite Measured by Time- Resolved Synchrotron X-ray Diffraction

    Science.gov (United States)

    Lopano, C. L.; Heaney, P. J.; Post, J. E.; Bandstra, J.; Brantley, S. L.

    2006-05-01

    Birnessite is the most abundant and chemically important layer-structure Mn-oxide phase found in soils, desert varnishes, and ocean nodules. It also is industrially important for use in battery technology and octahedral sieves. Due to the poorly crystalline nature of natural birnessite, synthetic analogues typically have been employed in studies that explore the structural response of birnessite to variations in interlayer composition. For this work, we measured changes in unit-cell parameters over time to quantify the degree of cation exchange as a function of concentration. Aqueous K+, Cs+, and Ba2+ cations at varying concentrations at pH 7 were exchanged for interlayer Na+ in synthetic birnessite (Na0.58(Mn4+1.42,Mn3+0.58)O4·1.5H2O) using a simple flow- through cell, and the exchange products were monitored via time-resolved X-ray powder diffraction at the National Synchrotron Light Source. Powder X-ray diffraction patterns were collected every 2-3 minutes. Rietveld analyses of X-ray diffraction patterns for K- and Ba-exchanged birnessite revealed a decrease in unit- cell volume over time. In contrast, Cs+ substitution increased cell volume. For all three cations, the crystallographic data indicate that exchange occurred in two stages. A rapid and dramatic change in unit-cell volume was followed by a modest adjustment over longer timescales. Fourier electron difference syntheses revealed that the rapid, initial stage of exchange was marked by re-configuration of the interlayer species, whereas the second, protracted phase of substitution represented ordering into the newly established interlayer positions. For the first time, we have modeled the kinetics of interlayer substitution in Na-birnessite. For purposes of comparison, we have employed a simple one-stage reaction (i.e., Na-birnessite → K-birnessite) and a two stage reaction (i.e,. Na-birnessite → K-birnessitedisordered → K- birnessiteordered). For exchange with 0.01 M KCl solutions, the single

  11. Reaction monitoring of cementing materials through multivariate techniques applied to time-resolved synchrotron X-Ray diffraction data

    Czech Academy of Sciences Publication Activity Database

    Taris, A.; Grosso, M.; Viani, Alberto; Brundu, M.; Guida, V.

    2015-01-01

    Roč. 43, May (2015), s. 895-900. ISBN 978-88-95608-34-1. ISSN 2283-9216 R&D Projects: GA MŠk(CZ) LO1219 Keywords : engineering controlled terms * least squares approximations * magnesium powder * multivariant analysis * potassium * reaction intermediates * X ray powder diffraction Subject RIV: AN - Psychology http://www.aidic.it/cet/15/43/150.pdf

  12. X-ray diffraction studies on single and mixed confectionery fats using synchrotron radiation

    Energy Technology Data Exchange (ETDEWEB)

    MacMillan, S.C.; Roberts, K.J.; Wells, M.; Polgreen, M.; Smith, I. [Heriot-Watt University, Edinburgh, (United Kingdom). Department of Mechanical and Chemical Engineering, Centre for Molecular and Interface Engineering

    1999-12-01

    Full text: Understanding and refining the molecular-scale processes involved in the manufacture of structured materials such as long-chain hydrocarbon compounds is important in many commercial areas such as the petrochemical, biochemical, food, pharmaceutical and soap industries. In such processes crystallisation is an important separation, purification and preparation technique. Despite this our knowledge of the crystallisation process itself is surprisingly limited. In order to improve the crystallisation of confectionery fats, the crystallisation of it`s main component, cocoa butter fat, must be properly understood. Cocoa butter fat can exhibit up to 6 polymorphic forms of different crystallographic structures with melting points varying from 17.3 deg C to 36.3 deg C. During the production of chocolate it is essential to control the polymorphic form of fats present, in order to produce a final product with the correct physical and rheological properties. Both shear rate and temperature are thought to play a crucial role in this process. The most widely used method for studying polymorphism is X-ray diffraction. Typical X-ray diffraction patterns of fats exhibit two groups of diffraction lines corresponding to the long and short spacings. The long spacings correspond to the planes formed by the methyl end groups and are dependent on the chain length and the angle of tilt of the component fatty acids of the glyceride molecules. The short spacings refer to the cross sectional packing of the hydrocarbon chain and are independent of the chain length. The relationship between crystallisation rate, polymorphic form, shear and the fat composition has for the first time been quantified, which will enable more accurate control of the polymorhic form in chocolate production. This has been achieved by developing an improved in-situ cell for X-ray studies. The X-ray studies are necessary for the examination of on-line studies under well controlled conditions of temperature

  13. X-ray diffraction studies on single and mixed confectionery fats using synchrotron radiation

    International Nuclear Information System (INIS)

    MacMillan, S.C.; Roberts, K.J.; Wells, M.; Polgreen, M.; Smith, I.

    1999-01-01

    Full text: Understanding and refining the molecular-scale processes involved in the manufacture of structured materials such as long-chain hydrocarbon compounds is important in many commercial areas such as the petrochemical, biochemical, food, pharmaceutical and soap industries. In such processes crystallisation is an important separation, purification and preparation technique. Despite this our knowledge of the crystallisation process itself is surprisingly limited. In order to improve the crystallisation of confectionery fats, the crystallisation of it's main component, cocoa butter fat, must be properly understood. Cocoa butter fat can exhibit up to 6 polymorphic forms of different crystallographic structures with melting points varying from 17.3 deg C to 36.3 deg C. During the production of chocolate it is essential to control the polymorphic form of fats present, in order to produce a final product with the correct physical and rheological properties. Both shear rate and temperature are thought to play a crucial role in this process. The most widely used method for studying polymorphism is X-ray diffraction. Typical X-ray diffraction patterns of fats exhibit two groups of diffraction lines corresponding to the long and short spacings. The long spacings correspond to the planes formed by the methyl end groups and are dependent on the chain length and the angle of tilt of the component fatty acids of the glyceride molecules. The short spacings refer to the cross sectional packing of the hydrocarbon chain and are independent of the chain length. The relationship between crystallisation rate, polymorphic form, shear and the fat composition has for the first time been quantified, which will enable more accurate control of the polymorhic form in chocolate production. This has been achieved by developing an improved in-situ cell for X-ray studies. The X-ray studies are necessary for the examination of on-line studies under well controlled conditions of temperature

  14. A flow cell for in situ synchrotron x-ray diffraction studies of scale formation under Bayer processing conditions

    Science.gov (United States)

    Webster, Nathan A. S.; Madsen, Ian C.; Loan, Melissa J.; Scarlett, Nicola V. Y.; Wallwork, Kia S.

    2009-08-01

    The design, construction, and commissioning of a stainless steel flow cell for in situ synchrotron x-ray diffraction studies of scale formation under Bayer processing conditions is described. The use of the cell is demonstrated by a study of Al(OH)3 scale formation on a mild steel substrate from synthetic Bayer liquor at 70 °C. The cell design allows for interchangeable parts and substrates and would be suitable for the study of scale formation in other industrial processes.

  15. Two strain-hardening mechanisms in nanocrystalline austenitic steel: An in situ synchrotron X-ray diffraction study

    International Nuclear Information System (INIS)

    Schloth, P.; Weisser, M.A.; Van Swygenhoven, H.; Van Petegem, S.; Susila, P.; Subramanya Sarma, V.; Murty, B.S.; Lauterbach, S.; Heilmaier, M.

    2012-01-01

    The mechanical behaviour of nanocrystalline austenitic steels with and without yttria particles was investigated using in situ synchrotron diffraction during tensile deformation. Two different strain-hardening regimes were found. The first regime can be assigned predominantly to a martensitic phase transformation, the second to deformation twinning in the fragmented retained austenite. The kinetics of martensitic phase transformation is remarkably enhanced in the nanocrystalline structure.

  16. In situ room temperature tensile deformation of a 1% CrMoV bainitic steel using synchrotron and neutron diffraction

    International Nuclear Information System (INIS)

    Weisser, M.A.; Evans, A.D.; Van Petegem, S.; Holdsworth, S.R.; Van Swygenhoven, H.

    2011-01-01

    Neutron and synchrotron X-ray diffraction spectra have been acquired during room temperature tensile deformation of a creep-resistant bainitic 1% CrMoV steel, in order to study the evolution of internal microstresses and load-sharing mechanisms between the ferrite matrix and the various carbides. Cementite takes load from the plastifying matrix at the onset of macroscopic plasticity resulting in residual interphase stresses. Single peak fitting indicates an elastic anisotropic behaviour of cementite.

  17. Clay pigment structure characterisation as a guide for provenance determination--a comparison between laboratory powder micro-XRD and synchrotron radiation XRD.

    Science.gov (United States)

    Švarcová, Silvie; Bezdička, Petr; Hradil, David; Hradilová, Janka; Žižak, Ivo

    2011-01-01

    Application of X-ray diffraction (XRD)-based techniques in the analysis of painted artworks is not only beneficial for indisputable identification of crystal constituents in colour layers, but it can also bring insight in material crystal structure, which can be affected by their geological formation, manufacturing procedure or secondary changes. This knowledge might be helpful for art historic evaluation of an artwork as well as for its conservation. By way of example of kaolinite, we show that classification of its crystal structure order based on XRD data is useful for estimation of its provenance. We found kaolinite in the preparation layer of a Gothic wall painting in a Czech church situated near Karlovy Vary, where there are important kaolin deposits. Comparing reference kaolin materials from eight various Czech deposits, we found that these can be differentiated just according to the kaolinite crystallinity. Within this study, we compared laboratory powder X-ray micro-diffraction (micro-XRD) with synchrotron radiation X-ray diffraction analysing the same real sample. We found that both techniques led to the same results.

  18. Structural anomalies in undoped gallium arsenide observed in high-resolution diffraction imaging with monochromatic synchrotron radiation

    Science.gov (United States)

    Steiner, B.; Kuriyama, M.; Dobbyn, R. C.; Laor, U.; Larson, D.

    1989-01-01

    Novel, streak-like disruption features restricted to the plane of diffraction have recently been observed in images obtained by synchrotron radiation diffraction from undoped, semi-insulating gallium arsenide crystals. These features were identified as ensembles of very thin platelets or interfaces lying in (110) planes, and a structural model consisting of antiphase domain boundaries was proposed. We report here the other principal features observed in high resolution monochromatic synchrotron radiation diffraction images: (quasi) cellular structure; linear, very low-angle subgrain boundaries in (110) directions, and surface stripes in a (110) direction. In addition, we report systematic differences in the acceptance angle for images involving various diffraction vectors. When these observations are considered together, a unifying picture emerges. The presence of ensembles of thin (110) antiphase platelet regions or boundaries is generally consistent not only with the streak-like diffraction features but with the other features reported here as well. For the formation of such regions we propose two mechanisms, operating in parallel, that appear to be consistent with the various defect features observed by a variety of techniques.

  19. Synchrotron X-ray diffraction investigations on strains in the oxide layer of an irradiated Zircaloy fuel cladding

    Science.gov (United States)

    Chollet, Mélanie; Valance, Stéphane; Abolhassani, Sousan; Stein, Gene; Grolimund, Daniel; Martin, Matthias; Bertsch, Johannes

    2017-05-01

    For the first time the microstructure of the oxide layer of a Zircaloy-2 cladding after 9 cycles of irradiation in a boiling water reactor has been analyzed with synchrotron micro-X-ray diffraction. Crystallographic strains of the monoclinic and to some extent of the tetragonal ZrO2 are depicted through the thick oxide layer. Thin layers of sub-oxide at the oxide-metal interface as found for autoclave-tested samples and described in the literature, have not been observed in this material maybe resulting from irradiation damage. Shifts of selected diffraction peaks of the monoclinic oxide show that the uniform strain produced during oxidation is orientated in the lattice and displays variations along the oxide layer. Diffraction peaks and their shifts from families of diffracting planes could be translated into a virtual tensor. This virtual tensor exhibits changes through the oxide layer passing by tensile or compressive components.

  20. The structure of octofluoronaphthalene at high pressures investigated by neutron powder diffraction

    International Nuclear Information System (INIS)

    Mackenzie, G.A.; Buras, B.

    1977-01-01

    The structure of the molecular crystal octofluoronaphthalene at high pressures has been studied by neutron powder diffraction. Evidence was found at about 0.8 kbar for a structural phase transition similar to that which occurs at 266.5 K at atmospheric pressure. The structure at atmospheric pressure and at 2 and 4 kbar has been refined using the powder profile refinement program EDINP. There is evidence for a further structural charge between 4 and 6 kbar, confirmed by measurements at 16 kbar, but there is insufficient data for a detailed analysis of this change. (Auth.)

  1. An in situ Study of NiTi Powder Sintering Using Neutron Diffraction

    OpenAIRE

    Chen, Gang; Liss, Klaus-Dieter; Cao, Peng

    2015-01-01

    This study investigates phase transformation and mechanical properties of porous NiTi alloys using two different powder compacts (i.e., Ni/Ti and Ni/TiH2) by a conventional press-and-sinter means. The compacted powder mixtures were sintered in vacuum at a final temperature of 1373 K. The phase evolution was performed by in situ neutron diffraction upon sintering and cooling. The predominant phase identified in all the produced porous NiTi alloys after being sintered at 1373 K is B2 NiTi phase...

  2. Accommodation stresses in hydride precipitates by synchrotron x-ray diffraction

    International Nuclear Information System (INIS)

    Santisteban, J R; Vicente, M A; Vizcaino, P; Banchik, A D; Almer, J

    2012-01-01

    Hydride-forming materials (Zr, Ti, Nb, etc) are affected by a sub-critical crack growth mechanism that involves the diffusion of H to the stressed region ahead of a crack, followed by nucleation and fracture of hydrides at the crack tip [1]. The phenomenon is intermittent, with the crack propagating through the hydride and stopping when it reaches the matrix. By repeating these processes, the crack propagates through a component at a rate that is highly dependent on the temperature history of the component. Most research effort to understand this phenomenon has occurred within the nuclear industry, as it affects the safe operation of pressure tubes (Zr2.5%Nb) and the long-term storage of nuclear fuel (Zircaloy cladding). Stress-induced hydride formation is a consequence of the volume dilatation that accompanies hydride formation (of the order of 15%), which is elastoplastically accommodated by the matrix and precipitate. Compressive stresses are expected within hydride precipitates due to the constraint imposed by the matrix. Such 'accommodation' stresses are essential ingredients in all theoretical models developed to assess the crack growth rate dependence on operational variables such as temperature, applied stress intensity factor, or overall H concentration [2]. Yet little experimental information is available about the magnitude and directionality of such accommodation stresses. Synchrotron X-ray diffraction is the only technique capable of quantifying such stresses. Here we briefly describe the fundaments of the technique, when used through an area detector placed in transmission geometry. The results of the experiments have allowed us to produce a comprehensive picture about the magnitude and origin of accommodation stresses in δ zirconium hydride platelets (author)

  3. Crystallography of hydrogen-containing compounds: realizing the potential of neutron powder diffraction.

    Science.gov (United States)

    Weller, Mark T; Henry, Paul F; Ting, Valeska P; Wilson, Chick C

    2009-06-07

    Hydrogen forms more compounds than any other element in the Periodic Table, yet methods for accurately, precisely and rapidly determining its position in a crystal structure are not readily available. The latest generation of high-flux neutron powder diffractometers, operating under optimised collection geometries, allow hydrogen positions to be extracted from the diffraction patterns of polycrystalline hydrogenous compounds without resorting to isotopic substitution. Neutron powder diffraction for hydrogenous materials has a wide range of applications within chemistry. These include the study of hydrogen-energy materials, coordination and organometallic compounds, hydrogen-bonded structures and ferroelectrics, geomaterials, zeolites and small molecule organics, such as simple sugars and amino acids. The technique is particularly well suited to parametric studies, for example as a function of temperature or pressure, where changes in hydrogen bonding patterns or decompositions involving hydrogen-containing molecules, such as water, are monitored.

  4. Real-time powder diffraction studies of energy materials under non-equilibrium conditions

    Energy Technology Data Exchange (ETDEWEB)

    Peterson, Vanessa K.; Auckett, Josie E.; Pang, Wei-Kong

    2017-09-01

    Energy materials form the central part of energy devices. An essential part of their function is the ability to reversibly host charge or energy carriers, and analysis of their phase composition and structure in real time under non-equilibrium conditions is mandatory for a full understanding of their atomic-scale functional mechanism. Real-time powder diffraction is increasingly being applied for this purpose, forming a critical step in the strategic chemical engineering of materials with improved behaviour. This topical review gives examples of real-time analysis using powder diffraction of rechargeable battery electrodes and porous sorbent materials used for the separation and storage of energy-relevant gases to demonstrate advances in the insights which can be gained into their atomic-scale function.

  5. Neutron powder diffraction studies of Hydrogen and Denterium in Palladium Phosphides

    International Nuclear Information System (INIS)

    Andersson, Y.

    1986-01-01

    The use of the Rietveld-type profile refinements on neutron powder diffraction intensity data for determining crystallographic positions of hydrogen and deuterium in metal hydrides is illustrated by results obtained on some hydrogenated and deuterated palladium phosphides. The structural features of the solid solutions of hydrogen and deuterium in Pd/sb15/P/sb2/ Pd/sb6/P and Pd/sb3/P/sb1-u/ (0< u<0.28) are briefly presented and discussed

  6. A high-resolution neutron powder diffraction study of neodymium doping in barium cerate

    DEFF Research Database (Denmark)

    Knight, K.S.; Bonanos, N.

    1995-01-01

    High-resolution neutron powder diffraction data have been collected on 6 perovskites of composition BaCe1-xNdxO3-x/(2), with 0 less than or equal to x less than or equal to 0.2, in which structural phase transitions Pmcn-->P4/mbm at x=0.05, and P4/mbm-->Pm3m at x=0.1, were inferred from a recent ...

  7. Calculated powder x-ray diffraction data for three tantalum tungstates

    International Nuclear Information System (INIS)

    Holcombe, C.E. Jr.

    1976-11-01

    A study was made of computer-simulated powder x-ray diffraction data for Ta 22 W 4 O 67 , Ta 2 WO 8 , and Ta 16 W 18 O 94 --the three compounds in the Ta 2 O 5 --WO 3 system from 27 to 69 mole percent WO 3 . The crystal structures of Ta 2 WO 8 and one form of Ta 16 W 18 O 94 (Type B) were deduced from reported data. 8 tables

  8. High-pressure and high-temperature powder diffraction on molybdenum diphosphide, MoP2

    International Nuclear Information System (INIS)

    Soto, V.; Knorr, K.; Ehm, L.; Baehtz, C.; Winkler, B.; Avalos-Borja, M.

    2004-01-01

    The isothermal compressibility and bulk thermal expansion of molybdenum diphosphide, MoP 2 , were measured by in-situ X-ray powder diffraction from ambient conditions to 6.8 GPa and 839 K, respectively. A small anisotropy of the compressibilities in MoP 2 appears to be governed by non-bonding interactions in this layer-like material. The thermal expansion data are compared to molybdenum phosphide, MoP, which was measured to 1262 K. (orig.)

  9. Structure determination of two structural analogs, named 3-[1-(2-fluoro-4-biphenyl)ethyl]-6-(4-fluorophenyl)-1,2,4-triazolo[3,4-b]-1,3,4-thiadiazole (C23H16F2N4S) and 3-[1-(2-fluoro-4-biphenyl)ethyl]-6-(4-chlorophenyl)-1,2,4-triazolo[3,4-b]-1,3,4-thiadiazole (C23H16ClFN4S) by synchrotron X-ray powder diffraction

    Energy Technology Data Exchange (ETDEWEB)

    Gündoğdu, Gülsüm; Aytaç, Sevim Peri; Müller, Melanie; Tozkoparan, Birsen; Kaynak, Filiz Betül

    2017-12-01

    Two novel compounds, 3-[1-(2-fluoro-4-biphenyl)ethyl]-6-(4-fluorophenyl)-1,2,4-triazolo[3,4-b]-1,3,4-thiadiazole (C23H16F2N4S) (1) and 3-[1-(2-fluoro-4-biphenyl)ethyl]-6-(4-chlorophenyl)-1,2,4-triazolo[3,4-b]-1,3,4-thiadiazole (C23H16ClFN4S) (2), have been designed and synthesized as cytotoxic agents. The compounds were characterized by infrared, proton nuclear magnetic resonance, mass spectral data, elemental analysis and X-ray powder diffraction. The present study comprises spectral data and crystal structures of these novel compounds determined from synchrotron X-ray powder diffraction data. The structure solutions were obtained by simulated annealing. The final structures were achieved by Rietveld refinement using soft restraints for all bond lengths, bond angles, and planar groups. Both compounds crystallize in space group$P\\bar 1$,Z= 2, with the unit-cell parametersa= 6.37433(9),b= 11.3641(2),c= 14.09115(19) Å,α= 80.1740(8)°,β= 85.1164(8)°,γ= 80.9831(10)°,V= 991.55(3) Å3of compound (1) anda= 6.53736(6),b= 11.55725(15),c= 14.01373(13) Å,α= 80.3323(7)°,β= 84.8939(6)°,γ= 79.3954(8)°,V= 1024.08(2) Å3of compound (2). Structural analyses reveal that the title compounds are isostructural.

  10. BOOK REVIEW: Analysis of Residual Stress by Diffraction Using Neutron and Synchrotron Radiation

    Science.gov (United States)

    Fitzpatrick, ed M. E.; Lodini, A.

    2003-09-01

    The presence of residual stresses within engineering components is often a key feature in determining their usable lifetimes and failure characteristics. Residual surface compression can, for example, restrict the propagation of surface cracks through the bulk. As a consequence, it is essential to characterize the magnitude and spatial distribution of residual stresses and, at least for non-destructive testing, this is most widely achieved using diffraction of neutron and high energy synchrotron radiations. This book aims to provide a detailed description of the methodology used to determine residual stresses. The major emphasis is placed on the neutron method, this being the more widely established approach at present. It contains 20 chapters contributed by 23 authors, divided into five major parts. The overall layout is very logical, with the first part giving a general introduction to the use of neutrons and x-rays for materials research and summarizing the methods used for their production. Part 2 considers the more specific aspects of extracting the residual stress distribution within a bulk sample and includes some valuable comments on a number of potential experimental problems, such as the determination of the stress-free lattice parameter and the effects of broadening of the Bragg peaks. The experimental facilities currently available or under development are described in part 3, with the remaining two parts devoted to general and specific applications of the residual stress measurement technique. As expected with such a large number of different authors, there is some variation in style and quality. However, the text is generally easy to follow and, more importantly, it is largely free of the problems of inconsistent notation and dupication of material that can afflict multi-authored texts. My only negative comment concerns the latter portion of the book devoted to specific applications of the technique, which is illustrative rather than comprehensive. In

  11. Characterization of actinide bonding in Th(S2PMe2)4 by synchrotron X-ray diffraction

    International Nuclear Information System (INIS)

    Iversen, B.B.; Larsen, F.K.; Pinkerton, A.A.; Martin, A.; Darovsky, A.; Reynolds, P.A.

    1998-01-01

    Extensive synchrotron (28 K) and conventional sealed-tube (9 K) X-ray diffraction data have been collected on Th(S 2 PMe 2 ) 4 . Modeling of the electron density of the complex shows the bonding is quite ionic with little diffuse f or d type bonding density. Furthermore a large polarization of the Th core is observed revealing some 5d-like involvement in the bonding. High-quality ab initio density functional calculations are not able to reproduce these features and instead predict rather covalent bonding with considerable 6d-5f mixing. The study suggests that this theoretical method exaggerates the covalent nature of actinide bonds. It is shown that the most direct measure of covalence -- charge transfer and electron distributions -- can be usefully estimated by X-ray diffraction even in this most unfavorable of cases, where many actinide core electrons are present. The use of very low temperature data is crucial in the study of heavy metal complexes in order to minimize systematic errors such as thermal diffuse scattering and anharmonicity. The fact that accurate synchrotron radiation diffraction data can be measured within days makes studies of compounds beyond the first transition series more frequently within reach

  12. Hybrid Powder - Single Crystal X-Ray Diffraction Instrument for Planetary Mineralogical Analysis of Unprepared Samples, Phase I

    Data.gov (United States)

    National Aeronautics and Space Administration — We propose to develop a planetary exploration XRD/XRF instrument based on a hybrid diffraction approach that complements powder XRD analysis, similar to that of the...

  13. A new parallel and GPU version of a TREOR-based algorithm for indexing powder diffraction data

    Czech Academy of Sciences Publication Activity Database

    Šimeček, I.; Rohlíček, Jan; Zahradnický, T.; Langr, D.

    2015-01-01

    Roč. 48, Feb (2015), 166-170 ISSN 0021-8898 Institutional support: RVO:68378271 Keywords : indexing powder diffraction * TREOR algorithm * GPGPU Subject RIV: CB - Analytical Chemistry, Separation Impact factor: 3.720, year: 2014

  14. Synchrotron infrared microspectroscopy imaging using a multi-element detector (IRMSI-MED) for diffraction-limited chemical imaging

    Energy Technology Data Exchange (ETDEWEB)

    Nasse, Michael J. [Department of Physics, University of Wisconsin-Milwaukee, Milwaukee, WI 53211 (United States); Synchrotron Radiation Center, University of Wisconsin-Madison, Stoughton, WI 53589 (United States); Reininger, Ruben [Synchrotron Radiation Center, University of Wisconsin-Madison, Stoughton, WI 53589 (United States); Scientific Answers and Solutions, Madison, WI 53711 (United States); Kubala, Tim; Janowski, Sebastian [Synchrotron Radiation Center, University of Wisconsin-Madison, Stoughton, WI 53589 (United States); Hirschmugl, Carol [Department of Physics, University of Wisconsin-Milwaukee, Milwaukee, WI 53211 (United States)], E-mail: cjhirsch@uwm.edu

    2007-11-11

    University of Wisconsin-Milwaukee is designing and installing a mid-infrared beamline, IRMSI-MED, that will extract 320(h)x25(v) mrad{sup 2} from a bending magnet (BM) at the Synchrotron Radiation Center. The BM radiation, collected with 12 toroidal mirrors and collimated with paraboloidal mirrors, illuminates a spot of 60x40 {mu}m{sup 2} at the sample plane of a commercial IR microscope. The microscope is equipped with a multi-element detector (MED) that will provide the opportunity to obtain chemical images with diffraction-limited resolution of the illuminated area in under a minute.

  15. X-ray diffraction measurement of liquid As2Se3 by using third-generation synchrotron radiation source

    OpenAIRE

    Kajihara, Yukio; Inui, Masanori; Matsuda, Kazuhiro; Tamura, Kozaburo; Hosokawa, Shinya

    2007-01-01

    X-ray diffraction (XD) measurements of liquid As2Se3 were carried out in the temperature range up to 1600◦C where the temperature is well beyond the semiconductor to metal (SC-M) transition temperature around 1000◦C . The measurements were done by using third-generation synchrotron radiation source at SPring-8 and the obtained structure factors have much improvements over the previous XD measurements by using in house X-ray sources with regard to the momentum transfer range and the data stati...

  16. Performances of synchrotron X-ray monochromators under heat load. Part 2. Application of the Takagi-Taupin diffraction theory

    CERN Document Server

    Mocella, V; Freund, A K; Hoszowska, J; Zhang, L; Epelboin, Y

    2001-01-01

    The aim of this work is to generate the rocking curves of monochromators exposed to heat load in synchrotron radiation beams with a computer code performing diffraction calculations based on the theory of Takagi and Taupin. The model study starts with the calculation of deformation by finite element analysis and from an accurate characterization of the incident wave and includes the simulation of the wavefront propagation between the first and the second crystal (analyzer) of a double crystal monochromator. A monochromatic plane wave as well as a polychromatic spherical wave approach is described. The theoretical predictions of both methods are compared with experimental data measured in Bragg geometry and critically discussed.

  17. Performances of synchrotron X-ray monochromators under heat load. Part 2. Application of the Takagi-Taupin diffraction theory

    Energy Technology Data Exchange (ETDEWEB)

    Mocella, V.; Ferrero, C. E-mail: ferrero@esrf.fr; Freund, A.K.; Hoszowska, J.; Zhang, L.; Epelboin, Y

    2001-07-21

    The aim of this work is to generate the rocking curves of monochromators exposed to heat load in synchrotron radiation beams with a computer code performing diffraction calculations based on the theory of Takagi and Taupin. The model study starts with the calculation of deformation by finite element analysis and from an accurate characterization of the incident wave and includes the simulation of the wavefront propagation between the first and the second crystal (analyzer) of a double crystal monochromator. A monochromatic plane wave as well as a polychromatic spherical wave approach is described. The theoretical predictions of both methods are compared with experimental data measured in Bragg geometry and critically discussed.

  18. Creep deformation of Co-Re-Ta-C alloys with varying C content-investigated in-situ by simultaneous synchrotron radiation diffraction

    Czech Academy of Sciences Publication Activity Database

    Karge, L.; Gilles, R.; Mukherji, D.; Stark, A.; Beran, Přemysl; Schell, N.; Hofmann, M.; Strunz, Pavel; Hausler, J.; Rösler, J.

    2018-01-01

    Roč. 719, č. 3 (2018), s. 124-131 ISSN 0921-5093 Institutional support: RVO:61389005 Keywords : high temperature creep * Co alloys * synchrotron diffraction * neutron diffraction * dilatometer Subject RIV: BM - Solid Matter Physics ; Magnetism OBOR OECD: Condensed matter physics (including formerly solid state physics, supercond.) Impact factor: 3.094, year: 2016

  19. Techniques for materials research with synchrotron radiation x-rays

    International Nuclear Information System (INIS)

    Bowen, D.K.

    1983-01-01

    A brief introductory survey is presented of the properties and generation of synchrotron radiation and the main techniques developed so far for its application to materials problems. Headings are:synchrotron radiation; X-ray techniques in synchrotron radiation (powder diffraction; X-ray scattering; EXAFS (Extended X-ray Absorption Fine Structure); X-ray fluorescent analysis; microradiography; white radiation topography; double crystal topography); future developments. (U.K.)

  20. Fast X-ray powder diffraction on I11 at Diamond.

    Science.gov (United States)

    Thompson, Stephen P; Parker, Julia E; Marchal, Julien; Potter, Jonathan; Birt, Adrian; Yuan, Fajin; Fearn, Richard D; Lennie, Alistair R; Street, Steven R; Tang, Chiu C

    2011-07-01

    The commissioning and performance characterization of a position-sensitive detector designed for fast X-ray powder diffraction experiments on beamline I11 at Diamond Light Source are described. The detecting elements comprise 18 detector-readout modules of MYTHEN-II silicon strip technology tiled to provide 90° coverage in 2θ. The modules are located in a rigid housing custom designed at Diamond with control of the device fully integrated into the beamline data acquisition environment. The detector is mounted on the I11 three-circle powder diffractometer to provide an intrinsic resolution of Δ2θ approximately equal to 0.004°. The results of commissioning and performance measurements using reference samples (Si and AgI) are presented, along with new results from scientific experiments selected to demonstrate the suitability of this facility for powder diffraction experiments where conventional angle scanning is too slow to capture rapid structural changes. The real-time dehydrogenation of MgH(2), a potential hydrogen storage compound, is investigated along with ultrafast high-throughput measurements to determine the crystallite quality of different samples of the metastable carbonate phase vaterite (CaCO(3)) precipitated and stabilized in the presence of amino acid molecules in a biomimetic synthesis process.

  1. In situ observation and neutron diffraction of NiTi powder sintering

    International Nuclear Information System (INIS)

    Chen, Gang; Liss, Klaus-Dieter; Cao, Peng

    2014-01-01

    This study investigated NiTi powder sintering behaviour from elemental powder mixtures of Ni/Ti and Ni/TiH 2 using in situ neutron diffraction and in situ scanning electron microscopy. The sintered porous alloys have open porosities ranging from 2.7% to 36.0%. In comparison to the Ni/Ti compact, dehydrogenation occurring in the Ni/TiH 2 compact leads to less densification yet higher chemical homogenization only after high-temperature sintering. For the first time, direct evidence of the eutectoid phase transformation of NiTi at 620 °C is reported by in situ neutron diffraction. A comparative study of cyclic stress–strain behaviours of the porous NiTi alloys made from Ni/Ti and Ni/TiH 2 compacts indicate that the samples sintered from the Ni/TiH 2 compact exhibited a much higher porosity, larger pore size, lower fracture strength, lower close-to-overall porosity ratio and lower Young’s modulus. Instead of enhanced densification by the use of TiH 2 as reported in the literature, this study shows an adverse effect of TiH 2 on powder densification in NiTi

  2. In situ X-ray powder diffraction, synthesis, and magnetic properties of InVO3

    International Nuclear Information System (INIS)

    Lundgren, Rylan J.; Cranswick, Lachlan M.D.; Bieringer, Mario

    2006-01-01

    We report the first synthesis and high-temperature in situ X-ray diffraction study of InVO 3 . Polycrystalline InVO 3 has been prepared via reduction of InVO 4 using a carbon monoxide/carbon dioxide buffer gas. InVO 3 crystallizes in the bixbyite structure in space group Ia-3 (206) with a=9.80636(31) A with In 3+ /V 3+ disorder on the (8b) and (24d) cation sites. In situ powder X-ray diffraction experiments and thermal gravimetric analysis in a CO/CO 2 buffer gas revealed the existence of the metastable phase InVO 3 . Bulk samples with 98.5(2)% purity were prepared using low-temperature reduction methods. The preparative methods limited the crystallinity of this new phase to approximately 225(50) A. Magnetic susceptibility and neutron diffraction experiments suggest a spin-glass ground state for InVO 3 . - Graphical abstract: In situ powder X-ray diffractograms for the reduction of InVO 4 in CO/CO 2 . The three temperature regions show the conversion of InVO 4 to InVO 3 and final decomposition into In 2 O 3 and V 2 O 3

  3. Simulation and modeling of the powder diffraction pattern from nanoparticles: Studying the influence of surface strain

    Science.gov (United States)

    Beyerlein, Kenneth Roy

    Nanostructured materials are currently at the forefront of nearly every emerging industry, as they offer promising solutions to problems ranging from those facing energy technologies, to those concerning the structural integrity of materials. With all of these future applications, it is crucial that methods are developed which can offer accurate, and statistically reliable characterization of these materials in a reasonable amount of time. X-ray diffraction is one such method which is already widely available, and can offer further insight into the atomic structure, as well as, microstructure of nanomaterials. This thesis work is then focused on investigating how different structural features of nanoparticles influence the line profiles of the x-ray powder diffraction pattern. Due to their extremely small size, the contribution from crystallite size broadening becomes the dominating feature in an observed diffraction peak. Therefore, the theory of size broadening was critically reviewed concerning the considerations necessary when the crystallite size approaches a few nanometers. Furthermore, the analysis of synthesized shape controlled platinum nanoparticles was carried out using a developed line profile analysis routine, based on the Debye function analysis (DFA) approach, to determine the distribution of particle size and shape in the sample. The DFA method is based on the use of atomistic models to simulate the features in the powder diffraction pattern. The atomistic descriptions of molecular dynamics simulations was coupled with this approach, allowing for the further understanding of the pattern from nanoparticles. The techniques were developed to study how lattice dynamics, and the resulting thermal diffuse scattering, are affected by the small crystallite domains. Furthermore, the relaxation of structural models for nanoparticles by MD simulations allowed for the assessment of features which are a present in the powder pattern as a result of a strain

  4. A Spectrometer for X-Ray Energy-Dispersive Diffraction using Synchrotron Radiation

    DEFF Research Database (Denmark)

    Staun Olsen, Janus; Buras, B; Gerward, Leif

    1981-01-01

    Describes a white-beam X-ray energy-dispersive diffractometer built for Hasylab in Hamburg, FRG, using the synchrotron radiation from the electron storage ring DORIS. The following features of the instrument are discussed: horizontal or vertical scattering plane, collimators, sample environment, ...

  5. Determination of Ni(II) crystal structure by powder x-ray diffraction ...

    African Journals Online (AJOL)

    X-ray powder diffraction pattern was used to determine the length of the unit cell, “a”, the lattice structure type, and the number of atoms per unit cell of Ni(II) crystal. The “a” value was determined to be 23.66 ± 0.005 Å, particle size of 34.87 nm, volume 13.24 Å and Strain value ε = 9.8 x 10-3. The cell search on PXRD patterns ...

  6. Reflection-mode x-ray powder diffraction cell for in situ studies of electrochemical reactions

    International Nuclear Information System (INIS)

    Roberts, G.A.; Stewart, K.D.

    2004-01-01

    The design and operation of an electrochemical cell for reflection-mode powder x-ray diffraction experiments are discussed. The cell is designed for the study of electrodes that are used in rechargeable lithium batteries. It is designed for assembly in a glove box so that air-sensitive materials, such as lithium foil electrodes and carbonate-based electrolytes with lithium salts, can be used. The cell uses a beryllium window for x-ray transmission and electrical contact. A simple mechanism for compressing the electrodes is included in the design. Sample results for the cell are shown with a Cu Kα source and a position-sensitive detector

  7. Extending the reach of powder diffraction modelling by user defined macros

    CERN Document Server

    Scardi, Paolo

    2010-01-01

    The main focus of this special topic volume is the development and possibilities of the MACRO language within TOPAS, with a specific session dedicated to WPPM. The collection is presented here in the form of a ""macro tutorial"" for the benefit of the entire powder diffraction community. More than a collection of standard scientific papers, the contributions to this special issue provide methods, tutorials and practical suggestions and solutions for the proper use of TOPAS and WPPM in a number of applications; ranging from the most common to the most refined and specific cases.Readers will fin

  8. Location of adsorbed species in NO-reduction catalysts by high resolution neutron powder diffraction

    International Nuclear Information System (INIS)

    Fowkes, A.J.; Rosseinsky, M.J.

    1999-01-01

    Complete text of publication follows. Catalysts containing copper ion exchanged into zeolites are attracting considerable attention due to their efficiency for both NO decomposition and the selective catalytic reduction of NO x in so-called lean-burn conditions in automotive exhausts. This presentation will describe the application of in-situ high resolution neutron powder diffraction to study active sites in a Cu-zeolite Y catalyst active for NO decomposition. The study under NO pressure reveals the location of two distinct copper sites for sorption. The influence of copper oxidation state on the structure of both the pristine and NO-loaded zeolites will be discussed. (author)

  9. Neutron powder diffraction studies as a function of temperature of structure II hydrate formed from propane

    Science.gov (United States)

    Rawn, C.J.; Rondinone, A.J.; Chakoumakos, B.C.; Circone, S.; Stern, L.A.; Kirby, S.H.; Ishii, Y.

    2003-01-01

    Neutron powder diffraction data confirm that hydrate samples synthesized with propane crystallize as structure type II hydrate. The structure has been modeled using rigid-body constraints to describe C3H8 molecules located in the eight larger polyhedral cavities of a deuterated host lattice. Data were collected at 12, 40, 100, 130, 160, 190, 220, and 250 K and used to calculate the thermal expansivity from the temperature dependence of the lattice parameters. The data collected allowed for full structural refinement of atomic coordinates and the atomic-displacement parameters.

  10. Powder neutron diffraction studies by means of the KSN-2 diffractometer

    International Nuclear Information System (INIS)

    Vratislav, S.; Dlouha, M.

    1998-01-01

    Placed at the 2nd horizontal beam tube of the LVR-15 research reactor, KSN-2 is a double axis powder diffractometer used for structure and texture experiments with polycrystalline samples. The diffractometer is equipped with auxiliary devices such as a cryogenic apparatus, heater furnace, and texture goniometer. The diffraction patterns are treated by Rietveld analysis, and complete structural parameters are determined. Research activities are focused on neutron scattering in solid state physics and materials science. Applications to condensed matter cover a wide range, from the location of light atoms and cation distributions to magnetic structures and phase transitions. Some promising materials such as zeolites, perovskites and high-temperature superconductors were investigated

  11. The position sensitive 1D-160 detector for high resolution powder diffraction

    CERN Document Server

    Babichev, E A; Groshev, V R; Khabakhpashev, A G; Kolachev, G M; Porosev, V V; Savinov, G A; Ancharov, A I; Pirogov, B J; Sharafutdinov, M R; Tolochko, B P

    2001-01-01

    A detector with an angular aperture of 160 deg. based on multi-wire proportion chamber is presented. The detector can work either in full-aperture mode or in scanning mode with restricted aperture. In the first one, which is used for the investigation of fast-running processes, angular resolution is 0.05 deg. In the other mode for high resolution powder diffraction, angular resolution is 0.002 deg. The count rate is 1 MHz per channel. The detector operates in the 'movies' mode with as many as 8000 frames and a minimum frame time of 10 mu s.

  12. Structure of D2O ice VIII from in situ powder neutron diffraction

    International Nuclear Information System (INIS)

    Jorgensen, J.D.; Beyerlein, R.A.; Watanabe, N.; Worlton, T.G.

    1984-01-01

    Structural parameters for D 2 O ice VIII have been determined by Rietveld refinement of time-of-flight powder neutron diffraction data collected in situ at 28 kbar and -4 0 C. The D 2 O molecule has a bond length of 0.973 (11) A and a bond angle of 104(2) 0 . O--DxxxO bonds are slightly bent with an angle of 177(1) 0 . Thus, the D 2 O molecules in ice VIII are essentially identical to those observed in other high pressure ice structures for which accurate structural data are available

  13. Structural studies of human insulin cocrystallized with phenol or resorcinol via powder diffraction.

    Science.gov (United States)

    Karavassili, Fotini; Giannopoulou, Anastasia E; Kotsiliti, Eleni; Knight, Lisa; Norrman, Mathias; Schluckebier, Gerd; Drube, Lene; Fitch, Andrew N; Wright, Jonathan P; Margiolaki, Irene

    2012-12-01

    The effects of the ligands phenol and resorcinol on the crystallization of human insulin have been investigated as a function of pH. Powder diffraction data were used to characterize several distinct polymorphic forms. A previously unknown polymorph with monoclinic symmetry (P2(1)) was identified for both types of ligand with similar characteristics [the unit-cell parameters for the insulin-resorcinol complex were a = 114.0228 (8), b = 335.43 (3), c = 49.211 (6) Å, β = 101.531 (8)°].

  14. Ice Recrystallization in a Solution of a Cryoprotector and Its Inhibition by a Protein: Synchrotron X-Ray Diffraction Study.

    Science.gov (United States)

    Zakharov, Boris; Fisyuk, Alexander; Fitch, Andy; Watier, Yves; Kostyuchenko, Anastasia; Varshney, Dushyant; Sztucki, Michael; Boldyreva, Elena; Shalaev, Evgenyi

    2016-07-01

    Ice formation and recrystallization is a key phenomenon in freezing and freeze-drying of pharmaceuticals and biopharmaceuticals. In this investigation, high-resolution synchrotron X-ray diffraction is used to quantify the extent of disorder of ice crystals in binary aqueous solutions of a cryoprotectant (sorbitol) and a protein, bovine serum albumin. Ice crystals in more dilute (10 wt%) solutions have lower level of microstrain and larger crystal domain size than these in more concentrated (40 wt%) solutions. Warming the sorbitol-water mixtures from 100 to 228 K resulted in partial ice melting, with simultaneous reduction in the microstrain and increase in crystallite size, that is, recrystallization. In contrast to sorbitol solutions, ice crystals in the BSA solutions preserved both the microstrain and smaller crystallite size on partial melting, demonstrating that BSA inhibits ice recrystallization. The results are consistent with BSA partitioning into quasi-liquid layer on ice crystals but not with a direct protein-ice interaction and protein sorption on ice surface. The study shows for the first time that a common (i.e., not-antifreeze) protein can have a major impact on ice recrystallization and also presents synchrotron X-ray diffraction as a unique tool for quantification of crystallinity and disorder in frozen aqueous systems. Copyright © 2016 American Pharmacists Association®. Published by Elsevier Inc. All rights reserved.

  15. Polarized neutron powder diffraction studies of antiferromagnetic order in bulk and nanoparticle NiO

    DEFF Research Database (Denmark)

    Brok, Erik; Lefmann, Kim; Deen, Pascale P.

    2015-01-01

    In many materials it remains a challenge to reveal the nature of magnetic correlations, including antiferromagnetism and spin disorder. Revealing the spin structure in magnetic nanoparticles is further complicated by the large incoherent neutron scattering cross section from water adsorbed...... surface contribution to the magnetic anisotropy. Here we explore the potential use of polarized neutron diffraction to reveal the magnetic structure in NiO bulk and nanoparticle powders by applying the XYZ-polarization analysis method. Our investigations address in particular the spin orientation in bulk...... at the particle surfaces and by the broadening of diffraction peaks due to the finite crystallite size. Moreover, the spin structure in magnetic nanoparticles may deviate significantly from that of the corresponding bulk material because of the low-symmetry surroundings of surface atoms and the large relative...

  16. SCRAP - a computer program for the analysis of powder diffraction patterns

    International Nuclear Information System (INIS)

    Cooper, M.J.; Rouse, K.D.

    1981-03-01

    A new computer program (SCRAP) for the analysis of powder diffraction patterns is described. A least-squares fitting of the observed and calculated intensities for individual points on the diffraction profile is used to determine values for the integrated intensities of the peaks, as well as any specified profile parameters. Conventional least-squares analysis of the integrated intensities can then be used to refine the values of the structural parameters. Use of this program therefore overcomes the limitations of the Rietveld profile refinement program (Rietveld. Acta Cryst.; 22: 151 (1967) and J. Appl. Cryst.; 2: 65 (1969)), in particular the unreliability of the estimated standard deviation values given by the latter. (author)

  17. Rietveld refinement with time-of-flight powder diffraction data from pulsed neutron sources

    International Nuclear Information System (INIS)

    David, W.I.F.; Jorgensen, J.D.

    1990-10-01

    The recent development of accelerator-based pulsed neutron sources has led to the widespread use of the time-of-flight technique for neutron powder diffraction. The properties of the pulsed source make possible unusually high resolution over a wide range of d spacings, high count rates, and the ability to collect complete data at fixed scattering angles. The peak shape and other instrument characteristics can be accurately modelled, which make Rietveld refinement possible for complex structures. In this paper we briefly review the development of the Rietveld method for time-of-flight diffraction data from pulsed neutron sources and discuss the latest developments in high resolution instrumentation and advanced Rietveld analysis methods. 50 refs., 12 figs., 14 tabs

  18. Probing hydrogen positions in hydrous compounds: information from parametric neutron powder diffraction studies.

    Science.gov (United States)

    Ting, Valeska P; Henry, Paul F; Schmidtmann, Marc; Wilson, Chick C; Weller, Mark T

    2012-05-21

    We demonstrate the extent to which modern detector technology, coupled with a high flux constant wavelength neutron source, can be used to obtain high quality diffraction data from short data collections, allowing the refinement of the full structures (including hydrogen positions) of hydrous compounds from in situ neutron powder diffraction measurements. The in situ thermodiffractometry and controlled humidity studies reported here reveal that important information on the reorientations of structural water molecules with changing conditions can be easily extracted, providing insight into the effects of hydrogen bonding on bulk physical properties. Using crystalline BaCl2·2H2O as an example system, we analyse the structural changes in the compound and its dehydration intermediates with changing temperature and humidity levels to demonstrate the quality of the dynamic structural information on the hydrogen atoms and associated hydrogen bonding that can be obtained without resorting to sample deuteration.

  19. Fourier-filtering techniques for the analysis of high-resolution pulsed neutron powder diffraction data

    International Nuclear Information System (INIS)

    Richardson, J.W. Jr.; Faber, J. Jr.

    1985-01-01

    Rietveld profile refinements using high-resolution pulsed neutron powder diffraction data, collected at IPNS, often reveal broad intensity contributions from sources other than the crystalline materials being studied. Such non-crystalline intensity hampers standard Rietveld refinement, and its removal and/or identification is imperative for successful refinement of the crystalline structure. A Fourier-filtering technique allows removal of the non-crystalline scattering contributions to the overall scattering pattern and yields information about the noncrystalline material. In particular, Fourier transformation of residual intensities not accounted for by the Rietveld procedure results in a real-space correlation function similar to a radial distribution function (RDF). From the inverse Fourier transform of the correlation function a Fourier-filtered fit to the diffuse scattering is obtained. This mathematical technique was applied to data for crystalline quartz, amorphous silica, and to a simulated diffraction pattern for a mixture of the two phases. 7 refs., 4 figs., 1 tab

  20. Crystal structures of eight mono-methyl alkanes (C26–C32 via single-crystal and powder diffraction and DFT-D optimization

    Directory of Open Access Journals (Sweden)

    Lee Brooks

    2015-09-01

    Full Text Available The crystal structures of eight mono-methyl alkanes have been determined from single-crystal or high-resolution powder X-ray diffraction using synchrotron radiation. Mono-methyl alkanes can be found on the cuticles of insects and are believed to act as recognition pheromones in some social species, e.g. ants, wasps etc. The molecules were synthesized as pure S enantiomers and are (S-9-methylpentacosane, C26H54; (S-9-methylheptacosane and (S-11-methylheptacosane, C28H58; (S-7-methylnonacosane, (S-9-methylnonacosane, (S-11-methylnonacosane and (S-13-methylnonacosane, C30H62; and (S-9-methylhentriacontane, C32H66. All crystallize in space group P21. Depending on the position of the methyl group on the carbon chain, two packing schemes are observed, in which the molecules pack together hexagonally as linear rods with terminal and side methyl groups clustering to form distinct motifs. Carbon-chain torsion angles deviate by less than 10° from the fully extended conformation, but with one packing form showing greater curvature than the other near the position of the methyl side group. The crystal structures are optimized by dispersion-corrected DFT calculations, because of the difficulties in refining accurate structural parameters from powder diffraction data from relatively poorly crystalline materials.

  1. Analysis of an industrial production suspension of Bacillus lentus subtilisin crystals by powder diffraction: a powerful quality-control tool.

    Science.gov (United States)

    Frankaer, Christian G; Moroz, Olga V; Turkenburg, Johan P; Aspmo, Stein I; Thymark, Majbritt; Friis, Esben P; Stahl, Kenny; Nielsen, Jens E; Wilson, Keith S; Harris, Pernille

    2014-04-01

    A microcrystalline suspension of Bacillus lentus subtilisin (Savinase) produced during industrial large-scale production was analysed by X-ray powder diffraction (XRPD) and X-ray single-crystal diffraction (MX). XRPD established that the bulk microcrystal sample representative of the entire production suspension corresponded to space group P212121, with unit-cell parameters a = 47.65, b = 62.43, c = 75.74 Å, equivalent to those for a known orthorhombic crystal form (PDB entry 1ndq). MX using synchrotron beamlines at the Diamond Light Source with beam dimensions of 20 × 20 µm was subsequently used to study the largest crystals present in the suspension, with diffraction data being collected from two single crystals (∼20 × 20 × 60 µm) to resolutions of 1.40 and 1.57 Å, respectively. Both structures also belonged to space group P2(1)2(1)2(1), but were quite distinct from the dominant form identified by XRPD, with unit-cell parameters a = 53.04, b = 57.55, c = 71.37 Å and a = 52.72, b = 57.13, c = 65.86 Å, respectively, and refined to R = 10.8% and Rfree = 15.5% and to R = 14.1% and Rfree = 18.0%, respectively. They are also different from any of the forms previously reported in the PDB. A controlled crystallization experiment with a highly purified Savinase sample allowed the growth of single crystals of the form identified by XRPD; their structure was solved and refined to a resolution of 1.17 Å with an R of 9.2% and an Rfree of 11.8%. Thus, there are at least three polymorphs present in the production suspension, albeit with the 1ndq-like microcrystals predominating. It is shown how the two techniques can provide invaluable and complementary information for such a production suspension and it is proposed that XRPD provides an excellent quality-control tool for such suspensions.

  2. X-ray diffraction using synchrotron radiation on the G.I.L.D.A. beam line at the E.S.R.F

    Energy Technology Data Exchange (ETDEWEB)

    Balerna, A. [INFN, Laboratori Nazionali di Frascati, Rome (Italy); Meneghini, C. [INFN, Laboratori Nazionali di Frascati, Rome (Italy)]|[INFM, Genoa (Italy); Bordoni, S. [Rome Univ. `Tor Vergata` (Italy). Dip. di Fisica; Mobilio, S. [Rome Univ. III (Italy). Dip. di Fisica `E. Amaldi`

    1996-09-01

    The aim of this lecture is to make a short introduction on Synchrotron radiation, its history and main properties. The main components of a synchrotron radiation beam line will be described. The Italian beam line, General purpose Italian beam line Line for Diffraction and Absorption (G.I.L.D.A.) at the European Synchrotron Radiation Facility (E.S.R.F.) in Grenoble will be used as an example. The G.I.L.D.A. diffractometer will be described in detail reporting also some experimental results.

  3. X-ray diffraction using synchrotron radiation on the G.I.L.D.A. beam line at the E.S.R.F

    International Nuclear Information System (INIS)

    Balerna, A.; Bordoni, S.; Mobilio, S.

    1996-01-01

    The aim of this lecture is to make a short introduction on Synchrotron radiation, its history and main properties. The main components of a synchrotron radiation beam line will be described. The Italian beam line, General purpose Italian beam line Line for Diffraction and Absorption (G.I.L.D.A.) at the European Synchrotron Radiation Facility (E.S.R.F.) in Grenoble will be used as an example. The G.I.L.D.A. diffractometer will be described in detail reporting also some experimental results

  4. Water-cooled ion-milled diffraction gratings for the synchrotron radiation community

    Energy Technology Data Exchange (ETDEWEB)

    McKinney, W.R.; Shannon, C.L.; Shults, E.N.

    1993-08-01

    Key technical and strategic choices are reviewed, leading to the fabrication method of ion-milled grating grooves for the monochromators at the Advanced Light Source (ALS) at Lawrence Berkeley Laboratory (LBL), and for other synchrotrons. Several laboratories and their industrial partners have joined to manufacture gratings with essentially theoretical performance. Metrology -data and theoretical comparisons are given for square wave profile grating samples ion-milled into electroless nickel surfaces. The extensive capabilities of Hughes Aircraft in grating manufacture are reviewed.

  5. High resolution diffraction studies with synchrotron radiation on the structure of Li0.95Mn2.05O4 spinel

    International Nuclear Information System (INIS)

    Nowicki, W.; Darul, J.; Piszora, P.; Baehtz, C.; Wolska, E.

    2005-01-01

    Investigations of the structure transformations of lithium deficient Li 0.95 Mn 2.05 O 4 , in the temperature range of 10-1173 K, have been undertaken with X-ray powder diffraction, using synchrotron radiation, at the HASYLAB high-resolution diffractometer (beamline B2). Single phase spinel-like oxide was obtained by a solid state reaction between α-Mn 2 O 3 and Li 2 CO 3 at 1073 K, followed by rapid quenching of the sample in the solid CO 2 . At the room temperature, the lithium deficient sample (with x = 0.95 in Li x Mn 3-x O 4 ) shows a tetragonally distorted spinel lattice, with c/a = 0.98. No phase transition has been observed when temperature decreased and the sample remained tetragonal in the range 300-10 K. A reversible phase transition appears, however, during very mild heating of Li 0.95 Mn 2.05 O 4 above the room temperature. The tetragonal spinel structure (F4 1 /ddm) undergoes a transition into cubic form (Fd3m) at 393 K. A thermal treatment above 573 K causes a partial decomposition of the sample, resulting in a formation of a nearly stoichiometric LiMn 2 O 4 , with the admixture of manganese oxides

  6. A standardless method of quantitative ceramic analysis using X-ray powder diffraction

    International Nuclear Information System (INIS)

    Mazumdar, S.

    1999-01-01

    A new procedure using X-ray powder diffraction data for quantitative estimation of the crystalline as well as the amorphous phase in ceramics is described. Classification of the crystalline and amorphous X-ray scattering was achieved by comparison of the slopes at two successive points of the powder pattern at scattering angles at which the crystalline and amorphous phases superimpose. If the second slope exceeds the first by a stipulated value, the intensity is taken as crystalline; otherwise the scattering is considered as amorphous. Crystalline phase analysis is obtained by linear programming techniques using the concept that each observed X-ray diffraction peak has contributions from n component phases, the proportionate analysis of which is required. The method does not require the measurement of calibration data for use as an internal standard, but knowledge of the approximate crystal structure of each phase of interest in the mixture is necessary. The technique is also helpful in qualitative analysis because each suspected phase is characterized by the probability that it will be present when a reflection zone is considered in which the suspected crystalline phase could contribute. The amorphous phases are determined prior to the crystalline ones. The method is applied to ceramic materials and some results are presented. (orig.)

  7. Studies of clays and clay minerals using x-ray powder diffraction and the Rietveld method

    International Nuclear Information System (INIS)

    Bish, D.L.

    1993-01-01

    The Rietveld method was originally developed (Rietveld, 1967, 1969) to refine crystal structures using neutron powder diffraction data. Since then, the method has been increasingly used with X-ray powder diffraction data, and today it is safe to say that this is the most common application of the method. The method has been applied to numerous natural and synthetic materials, most of which do not usually form crystals large enough for study with single-crystal techniques. It is the ability to study the structures of materials for which sufficiently large single crystals do not exist that makes the method so powerful and popular. It would thus appear that the method is ideal for studying clays and clay minerals. In many cases this is true, but the assumptions implicit in the method and the disordered nature of many clay minerals can limit titsapplicability. This chapter will describe the Rietveld method, emphasizing the assumptions important for the study of disordered materials, and it will outline the potential applications of the method to these minerals. These applications include, in addition to the refinement of crystal structures, quantitative analysis of multicomponent mixtures, analysis of peak broadening, partial structure solution, and refinement of unit-cell parameters

  8. Contribution of synchrotron diffraction for the study of the martensitic transformation in the steels;Apport de la diffraction synchrotron a l'etude de la transformation martensitique dans les aciers

    Energy Technology Data Exchange (ETDEWEB)

    Dehmas, M.; Bruneseaux, F.; Gautier, E.; Appolaire, B.; Denis, S.; Denand, B.; Settefrati, A. [Laboratoire de Science et Genie des Materiaux et de Metallurgie - LSG2M, Ecole des Mines, Parc de Saurupt, 54 - Nancy (France); Geandier, G.; Mauro, A. [PHYMAT Universite de Poitiers, SP2MI, 86 - Chasseneuil-Futuroscope (France); Peel, M.; Gonzales Aviles, G.; Buslaps, T. [ESRF, 38 - Grenoble (France); Peel, M. [FAME38, 38 - Grenoble (France)

    2009-07-01

    The number of studies dealing with the analysis of phase transformation using in situ Synchrotron high energy X-Ray diffraction is increasing. Indeed, the high energy beam allows a characterization in the volume, with a low acquisition time. Combined with an experimental set up allowing varying the temperature of the specimen with a simultaneous acquisition of the diffraction data, we get a powerful tool to characterize precisely the phase transformation sequences, the overall transformation kinetics, and in some specific cases to reach information on nucleation and growth. A simultaneous analysis of the cell parameters evolutions of each phase during the transformation process may also lead to additional knowledge on the transformation mechanisms. The proposed study is to increase our knowledge of martensitic transformation in steels. In this way, two steels were studied (i.e. Maraging steel with a low carbon amount and 35NiCrMo16 steel with a high amount carbon) by in situ high energy X-ray diffraction in order to follow the kinetics of the martensitic transformation, the evolutions of cell parameters as well as full width at half maximum of each phase. The effect of a stress on the kinetics of martensitic transformation for Maraging steel was also studied. The results are discussed and the mean cell parameter evolution of austenite is compared with a micro-mechanical calculation using a Mori Tanaka model. (authors)

  9. A variable-temperature sample container for low-temperature neutron powder diffraction

    International Nuclear Information System (INIS)

    Arzi, E.; Sandor, E.

    1983-01-01

    A variable-temperature sample container was developed for the neutron powder diffraction study of crystal structures and phase transitions in soldified gases. It consists of two coaxial tubes made of boron-free fused silica and fitted with heating coils and thermocouples. The exchange space between the tubes is filled with low-pressure helium gas controlled by two fine needle valves. Used in conjunction with a centre-stick-type liquid-helium cryostat and a proportional temperature controller, it maintains a powder sample of about 8 cm 3 volume at a constant temperature anywhere in the 4.2 to 77.4 K temperature range. Its stability is not worse than +-0.15 K and the liquid-helium consumption is about 1 litre a day above 17 K, increasing up to 6 litres a day at lower temperatures. It can also be used for the preparation of fine-grained powder samples directly from the gas phase. (Auth.)

  10. Synchrotron light; Lumiere synchrotron

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    2001-07-01

    'Synchrotron Light' is an interactive and detailed introduction to the physics and technology of the generation of coherent radiation from accelerators as well as to its widespread high-tech applications in science, medicine and engineering. The topics covered are the interaction of light and matter, the technology of synchrotron light sources, spectroscopy, imaging, scattering and diffraction of X-rays, and applications to materials science, biology, biochemistry, medicine, chemistry, food and pharmaceutical technology. All synchrotron light facilities are introduced with their home-page addresses. 'Synchrotron Light' provides an instructive and comprehensive multimedia learning tool for students, experienced practitioners and novices wishing to apply synchrotron radiation in their future work. Its multiple-entry points permit an easy exploration of the CD-Rom according to the users knowledge and interest. 2-D and 3-D animations and virtual reconstruction with computer-generated images guide visitors into the scientific and technical world of a synchrotron and into the applications of synchrotron radiation. This bilingual (English and French) CD-Rom can be used for self-teaching and in courses at various levels in physics, chemistry, engineering, and biology. (author)

  11. Real time observation of the hydrothermal crystallization of barium titanate using in situ neutron powder diffraction.

    Science.gov (United States)

    Walton, R I; Millange, F; Smith, R I; Hansen, T C; O'Hare, D

    2001-12-19

    The hydrothermal crystallization of barium titanate, BaTiO3, has been studied in situ by time-resolved powder neutron diffraction methods using the recently developed Oxford/ISIS hydrothermal cell. This technique has allowed the formation of the ferroelectric ceramic to be followed in a noninvasive manner in real time and under genuine reaction conditions. In a first set of experiments, Ba(OD)2-8D2O was reacted with two different titanium sources, either crystalline TiO2 (anatase) or amorphous TiO2-H2O in D2O, at 100-140 degrees C and the reaction studied using the POLARIS time-of-flight neutron powder diffractometer, at the ISIS Facility. In a second series of experiments, the reaction between barium chloride and crystalline TiO2 (anatase) in NaOD/D2O was studied at temperatures between 100 and 200 degrees C and at different deuterioxide concentrations using the constant-wavelength D20 neutron powder diffractometer at the Institut Laue Langevin. Quantitative growth and decay curves were determined from analysis of the integrated intensities of Bragg reflections of starting materials and product phases. In both sets of experiments the rapid dissolution of the barium source was observed, followed by dissolution of the titanium source before the onset of crystallization of barium titanate. Using a nucleation-growth model we are able to simulate the growth curve of barium titanate at three temperatures. Our results indicate the predominance of a homogeneous dissolution-precipitation mechanism for the hydrothermal formation of barium titanate, rather than other possible mechanisms that have been discussed in the literature. Analysis of the line widths of the Bragg reflections in the neutron diffraction data indicates that the particle size of the BaTiO3 product phase prepared from the amorphous TiO2-H2O is smaller than that prepared from crystalline TiO2 (anatase).

  12. About some practical aspects of X-ray diffraction : From powder to thin film

    Energy Technology Data Exchange (ETDEWEB)

    Valvoda, V. [Charles Univ. Prague (Czech Republic). Faculty of Mathematics and Physics

    1996-09-01

    Structure of thin films can be amorphous, polycrystalline or epitaxial, and the films can be prepared as a single layer films, multilayers or as graded films. A complete structure analysis of thin films by means of X-ray diffraction (XRD) usually needs more than one diffraction geometry to be used. Their principles, advantages and disadvantages will be shortly described, especially with respect to their different sampling depth and different response to orientation of diffracting crystallographic planes. Main differences in structure of thin films with respect to powder samples are given by a singular direction of their growth, by their adhesion to a substrate and often also by a simultaneous bombardment by atomic species during the growth. It means that a thermodynamically unstable atomic structures can be found too. These special features of growth of thin polycrystalline films are reflected in often found strong preferred orientation of grains and in residual stresses conserved in the films. The methods of structure analysis of thin films by XRD will be compared with other techniques which can supply structure images on different scales.

  13. Development of powder diffraction anomalous fine structure method and applications to electrode materials for rechargeable batteries

    International Nuclear Information System (INIS)

    Kawaguchi, Tomoya; Fukuda, Katsutoshi; Oishi, Masatsugu; Ichitsubo, Tetsu; Matsubara, Eiichiro; Mizuki, Jun'ichiro

    2015-01-01

    A powder diffraction anomalous fine structure (P-DAFS) method is developed both in analytical and experimental techniques and applied to cathode materials for lithium ion batteries. The DAFS method, which is an absorption spectroscopic technique through a scattering measurement, enables us to analyze the chemical states and the local structures of a certain element at different sites, thanks to the nature of x-ray diffraction, where the contributions from each site are different at each diffraction. Electrode materials for rechargeable batteries frequently exhibit the interchange between Li and a transition metal, which is known as the cation mixing phenomena. This cation mixing significantly affects the whole electrode properties; therefore, the site-distinguished understanding of the roles of the transition metal is essential for further material design by controlling and positively utilizing this cation mixing phenomenon. However, the developments of the P-DAFS method are required for the applications to the practical materials such as the electrode materials. In the present study, a direct analysis technique to extract the absorption spectrum from the scattering without using the conventional iterative calculations, fast and accurate measurement techniques of the P-DAFS method, and applications to a typical electrode material of Li 1-x Ni 1+x O 2 , which exhibits the significant cation mixing, are described. (author)

  14. Residual stress distribution in steel butt welds measured using neutron and synchrotron diffraction.

    Science.gov (United States)

    Paradowska, A M; Price, J W H; Finlayson, T R; Lienert, U; Walls, P; Ibrahim, R

    2009-03-25

    70 keV synchrotron radiation and thermal neutrons have been employed to investigate the residual stress characteristics in a fully restrained, steel, butt weld. The focus is on the values of the subsurface and through-thickness strain/stress variation in the middle of the weld. The advantages and limitations of the techniques have been addressed, in relation to the gauge volume, the stress-free reference sample and positioning. The measurement of residual stress around the weld achieved in this work significantly improves the resolution at which residual stress in welded components has been determined.

  15. 'Moving source': feasibility of diffraction experiment with nanosecond time resolution by the fast synchrotron radiation beam scanning

    CERN Document Server

    Tolochko, B P; Mezentsev, N A; Mishnev, S I

    2000-01-01

    We propose combination of electronical and X-ray optical scheme that will allow one to fulfil the diffraction experiment with a nanosecond time resolution. In this scheme, a few bunches of electrons will be in the nearest separatrixes. They will move inside the undulator along the different trajectories and at different moments t sub i. Each trajectory will have a different deviation above the stationary orbit. As a result there will be a shift of the synchrotron radiation (SR) generation point from the equilibrium position. So, a discretely moving source of SR will be created: the SR will be radiated at t sub i moment and from the ith point. For each ith trajectory of electrons (and for SR), a single-coordinate detector D sub i will be placed for diffracted radiation collecting from the ith point of the sample. So, every new X-ray diffraction image will be received within time interval t sub i sub - sub 1 -t sub i which is equal to a few nanoseconds. The exposure time may be as short as the electron bunch du...

  16. Processing of Bi-2212 and Nb$_3$Sn studied in situ by high energy synchrotron diffraction and micro-tomography

    CERN Document Server

    Kadar, Julian

    Next generation superconducting wires have been studied to obtain more information on the evolution of phase growth, crystallite size and strain state during wire processing. The high energy scattering beam line ID15 at the European Synchrotron Radiation Facility provides a very high flux of high energy photons for very fast in situ X-ray diffraction and micro-tomography studies of Bi-2212/Ag and Nb$_3$S/Cu wire samples. The typical wire processing conditions could be imitated in the X-ray transparent furnace at ID15 for diffraction and tomography studies. Efficient data analysis is mandatory in order to handle the very fast data acquisition rate. For this purpose an Excel-VBA based program was developed that allows a semi-automated fitting and tracking of peaks with pre-set constraints. With this method, more than one thousand diffraction patterns have been analysed to extract d-spacing, peak intensity and peak width values. X ray absorption micro tomograms were recorded simultaneously with the X-ray diffrac...

  17. Fast in situ phase and stress analysis during laser surface treatment: A synchrotron x-ray diffraction approach

    Science.gov (United States)

    Kostov, V.; Gibmeier, J.; Wilde, F.; Staron, P.; Rössler, R.; Wanner, A.

    2012-11-01

    An in situ stress analysis by means of synchrotron x-ray diffraction was carried out during laser surface hardening of steel. A single exposure set-up that based on a special arrangement of two fast silicon strip line detectors was established, allowing for fast stress analysis according to the sin2ψ x-ray analysis method. For the in situ experiments a process chamber was designed and manufactured, which is described in detail. First measurements were carried out at the HZG undulator imaging beamline (IBL, beamline P05) at the synchrotron storage ring PETRA III, DESY, Hamburg (Germany). The laser processing was carried out using a 6 kW high power diode laser system. Two different laser optics were compared, a Gaussian optic with a focus spot of ø 3 mm and a homogenizing optic with a rectangular spot dimension of 8 × 8 mm2. The laser processing was carried out using spot hardening at a heating-/cooling rate of 1000 K/s and was controlled via pyrometric temperature measurement using a control temperature of 1150 °C. The set-up being established during the measuring campaign allowed for this first realization data collection rates of 10Hz. The data evaluation procedure applied enables the separation of thermal from elastic strains and gains unprecedented insight into the laser hardening process.

  18. Direct Observations of Sigma Phase Formation in Duplex Stainless Steels using In Situ Synchrotron X-Ray Diffraction

    Energy Technology Data Exchange (ETDEWEB)

    Elmer, J W; Palmer, T A; Specht, E D

    2006-07-03

    The formation and growth of sigma phase in 2205 duplex stainless steel was observed and measured in real time using synchrotron radiation during 10 hr isothermal heat treatments at temperatures between 700 C and 850 C. Sigma formed in near-equilibrium quantities during the isothermal holds, starting from a microstructure which contained a balanced mixture of metastable ferrite and austenite. In situ synchrotron diffraction continuously monitored the transformation, and these results were compared to those predicted by thermodynamic calculations. Differences between the calculated and measured amounts of sigma, ferrite and austenite suggest that the thermodynamic calculations underpredict the sigma dissolution temperature by approximately 50 C. The data were further analyzed using a modified Johnson-Mehl-Avrami (JMA) approach to determine kinetic parameters for sigma formation over this temperature range. The initial JMA exponent, n, at low fractions of sigma was found to be approximately 7.0, however, towards the end of the transformation, n decreased to values of approximately 0.75. The change in the JMA exponent was attributed to a change in the transformation mechanism from discontinuous precipitation with increasing nucleation rate, to growth of the existing sigma phase after nucleation site saturation occurred. Because of this change in mechanism, it was not possible to determine reliable values for the activation energy and pre-exponential terms for the JMA equation. While cooling back to room temperature, the partial transformation of austenite resulted in a substantial increase in the ferrite content, but sigma retained its high temperature value to room temperature.

  19. Syntheses and crystal structure determination by X-ray powder diffraction of new compounds of Benzovesamicol

    International Nuclear Information System (INIS)

    Rukiah, M.; Assaad, Th.

    2012-06-01

    The compound 2,2,2-Trifluoro-N-(1a,2,7,7 a-tetra-hydronaphtho[2,3-b]oxiren-3-yl)- acetamide, C 1 2H 1 0F 3 NO 2 , an important precursor in the preparation of benzovesamicol analogues for the diagnosis of Alzheimers disease, was prepared by the epoxidation of 5,8-dihydronaphthalene-1-amine using 3-chloroperoxybenzoic acid. The structure was determined by X-ray powder diffraction, multinuclear NMR spectroscopy and FT-IR spectroscopy. A pair of molecules form intermolecular N- H...O hydrogen bonds, involving the amino and oxirene groups, to produce a dimer.The two racemic compounds (2RS,3RS)-5-amino-3-(4-phenylpiperazin-1-yl)-1,2,3,4 tetrahydronaphthalene-2-ol, C 2 0H 2 5N 3 O, (I) and (2RS,3RS)-5-amino-3-[4-(3- methoxyphenyl)piperazin-1-yl]-1,2,3,4-tetrahydronaphthalene-2-ol, C 2 1H 2 7N 3 O 2 , (II) important benzovesamicol analogues for the diagnosis of Alzheimer's disease, have been synthesized and characterized by FT-IR, and 1 H and 13 C NMR spectroscopic analyses. The crystal structures were analyses using powder diffraction as no suitable single crystal were obtained. The two compounds are racemic mixtures of enantiomers which crystallize in the monoclinic system in a centrosymmetric space group (P21/c). Crystallography, in particular powder X-ray diffraction, was pivotal in revealing that the enantio-resolution did not succeed. In two compounds, the piperazine ring has a chair conformation, while the cyclohexene ring assumes a half-chair conformation. In (I) the crystal packing is mediated by weak contacts, principally by complementary intermolecular N--H...O hydrogen bonds that connect successive molecules into a chain. Further stabilization is provided by weak C--H...N contacts and by a weak intermolecular C--H...π interaction. While in (II), the crystal packing is dominated by intermolecular O--H...N hydrogen bonding which links molecules along the c direction. (authors)

  20. Identification of cellulose fibres belonging to Spanish cultural heritage using synchrotron high resolution X-ray diffraction

    International Nuclear Information System (INIS)

    Herrera, L.K.; Justo, A.; Duran, A.; Haro, M.C.J. de; Franquelo, M.L.; Perez Rodriguez, J.L.

    2010-01-01

    A complete characterisation of fibres used in Spanish artwork is necessary to provide a complete knowledge of these natural fibres and their stage of degradation. Textile samples employed as painting supports on canvas and one sample of unprocessed plant material were chosen for this study. All the samples were investigated by synchrotron radiation X-ray diffraction (SR-XRD). Flax and cotton have the Cellulose I structure. The values of the crystalline index (CI) were calculated for both types of fibres. The structure of Cellulose IV was associated with the unprocessed plant material. The information obtained by SR-XRD was confirmed by laboratory techniques including scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FTIR). (orig.)

  1. X-ray diffraction analysis of rust layer on a weathering steel bridge with surface treatment using synchrotron radiation

    International Nuclear Information System (INIS)

    Yamashita, Masato; Hara, Shuichi; Kamimura, Takayuki; Miyuki, Hideaki; Sato, Masugu

    2007-01-01

    We have examined the structure of rust layer formed on a weathering steel bridge, to which the surface treatment, employing the effect of Cr 2 (SO 4 ) 3 sophisticatedly designed to form the protective goethite (α-FeOOH) rust layer which contains a certain amount of Cr, Cr-goethite, was applied in 1996, using X-ray diffraction at SPring-8 synchrotron radiation facility. It was shown that the formation of α-FeOOH was promoted and/or crystal growth of γ-FeOOH was suppressed by the surface treatment. The increase in the protective ability index (PAI) of the rust layer indicates that the protective goethite was predominantly formed under the effect of the surface treatment. In conclusion, it can be said that the surface treatment worked well to promote the formation of the protective goethite rust layer on the weathering steel bridge during the 10-year exposure. (author)

  2. Combined experimental powder X-ray diffraction and DFT data to obtain the lowest energy molecular conformation of friedelin

    Energy Technology Data Exchange (ETDEWEB)

    Oliveira, Djalma Menezes de; Mussel, Wagner da Nova; Duarte, Lucienir Pains; Silva, Gracia Divina de Fatima; Duarte, Helio Anderson; Gomes, Elionai Cassiana de Lima [Universidade Federal de Minas Gerais (UFMG), Belo Horizonte, MG (Brazil). Dept. de Quimica; Guimaraes, Luciana [Universidade Federal de Sao Joao Del-Rei (UFSJ), MG (Brazil). Dept. de Ciencias Naturais; Vieira Filho, Sidney A., E-mail: bibo@ef.ufop.br [Universidade Federal de Ouro Preto (UFOP), MG (Brazil). Dept. de Farmacia

    2012-07-01

    Friedelin molecular conformers were obtained by Density Functional Theory (DFT) and by ab initio structure determination from powder X-ray diffraction. Their conformers with the five rings in chair-chair-chair-boat-boat, and with all rings in chair, are energy degenerated in gas-phase according to DFT results. The powder diffraction data reveals that rings A, B and C of friedelin are in chair, and rings D and E in boat-boat, conformation. The high correlation values among powder diffraction data, DFT and reported single crystal data indicate that the use of conventional X-ray diffractometer can be applied in routine laboratory analysis in the absence of a single-crystal diffractometer. (author)

  3. Phase transformations in Ni/Ti multilayers investigated by synchrotron radiation-based x-ray diffraction

    Energy Technology Data Exchange (ETDEWEB)

    Cavaleiro, A.J., E-mail: andre.cavaleiro@dem.uc.pt [CEMUC, Department of Mechanical Engineering, University of Coimbra, R. Luís Reis Santos, 3030-788 Coimbra (Portugal); Ramos, A.S. [CEMUC, Department of Mechanical Engineering, University of Coimbra, R. Luís Reis Santos, 3030-788 Coimbra (Portugal); Martins, R.M.S. [CENIMAT/I3N, Department of Materials Science, Faculty of Sciences and Technology, University Nova de Lisboa, 2829-516 Caparica (Portugal); Instituto de Plasmas e Fusão Nuclear, Instituto Superior Técnico, Universidade de Lisboa, Av. Rovisco Pais, 1049-001 Lisboa (Portugal); LATR/IST/CTN – Campus Tecnológico e Nuclear, Estrada Nacional 10 ao km 139.7, 2695-066 Bobadela LRS (Portugal); Fernandes, F.M. Braz [CENIMAT/I3N, Department of Materials Science, Faculty of Sciences and Technology, University Nova de Lisboa, 2829-516 Caparica (Portugal); Morgiel, J. [Institute of Metallurgy and Materials Science, Polish Academy of Sciences, Reymonta 25, 30-059 Cracow (Poland); Baehtz, C. [Helmholtz Zentrum Dresden Rossendorf HZDR, Institute of Ion Beam Physics and Materials Research, D-01314 Dresden (Germany); Vieira, M.T. [CEMUC, Department of Mechanical Engineering, University of Coimbra, R. Luís Reis Santos, 3030-788 Coimbra (Portugal)

    2015-10-15

    X-ray diffraction using synchrotron radiation was used for real-time investigation of the phase evolution of Ni/Ti multilayer thin films during annealing. These multilayers were deposited onto Ti–6Al–4V substrates by dc magnetron sputtering from pure Ni and Ti targets. The deposition parameters were adjusted in order to obtain a near equiatomic chemical composition and modulation periods (Λ) below 25 nm. Along the entire thickness of the films, well-defined structures with alternate Ni- and Ti-rich layers are observed, even for Λ = 4 nm. In this case, a halo characteristic of an amorphous structure is obtained, while for Λ of 12 and 25 nm the as-deposited thin films are nanocrystalline being possible to identify the (111) Ni and (002) Ti diffraction peaks. The nanolayered structure vanishes during annealing due to interdiffusion followed by reaction. The reaction between Ni and Ti to produce NiTi in the cubic B2 structure occurs in a short delay of time and within a narrow temperature range. For Λ of 25, 12 and 4 nm, the reaction temperature is close to 320, 350 and 385 °C, respectively. For higher temperatures, in addition to the austenitic phase, the NiTi{sub 2} phase is identified. The diffusion of Ti from the substrate and Ni towards the substrate could favour the precipitation of NiTi{sub 2}. - Highlights: • Alternate Ni- and Ti-rich layers are observed, even for short periods. • Phase evolution was studied using synchrotron radiation XRD during annealing. • Ni and Ti reacted at ∼300–400 °C to form B2–NiTi in a single step. • The higher the period the lower the reaction temperature. • At higher temperatures NiTi{sub 2} was detected due to Ni diffusion towards Ti{sub 6}Al{sub 4}V.

  4. Puzzling Intergrowth in Cerium Nitridophosphate Unraveled by Joint Venture of Aberration-Corrected Scanning Transmission Electron Microscopy and Synchrotron Diffraction.

    Science.gov (United States)

    Kloß, Simon D; Neudert, Lukas; Döblinger, Markus; Nentwig, Markus; Oeckler, Oliver; Schnick, Wolfgang

    2017-09-13

    Thorough investigation of nitridophosphates has rapidly accelerated through development of new synthesis strategies. Here we used the recently developed high-pressure metathesis to prepare the first rare-earth metal nitridophosphate, Ce 4 Li 3 P 18 N 35 , with a high degree of condensation >1/2. Ce 4 Li 3 P 18 N 35 consists of an unprecedented hexagonal framework of PN 4 tetrahedra and exhibits blue luminescence peaking at 455 nm. Transmission electron microscopy (TEM) revealed two intergrown domains with slight structural and compositional variations. One domain type shows extremely weak superstructure phenomena revealed by atomic-resolution scanning TEM (STEM) and single-crystal diffraction using synchrotron radiation. The corresponding superstructure involves a modulated displacement of Ce atoms in channels of tetrahedra 6-rings. The displacement model was refined in a supercell as well as in an equivalent commensurate (3 + 2)-dimensional description in superspace group P6 3 (α, β, 0)0(-α - β, α, 0)0. In the second domain type, STEM revealed disordered vacancies of the same Ce atoms that were modulated in the first domain type, leading to sum formula Ce 4-0.5x Li 3 P 18 N 35-1.5x O 1.5x (x ≈ 0.72) of the average structure. The examination of these structural intricacies may indicate the detection limit of synchrotron diffraction and TEM. We discuss the occurrence of either Ce displacements or Ce vacancies that induce the incorporation of O as necessary stabilization of the crystal structure.

  5. Evaluation of crystallite size distribution by a capillary spinner-scan method in synchrotron powder diffractometry

    Science.gov (United States)

    Ida, Takashi; Goto, Taishi; Hibino, Hisashi

    2011-03-01

    A method to evaluate the effects of particle statistics in capillary-specimen transmission mode x-ray diffraction measurements has been developed. Average crystallite size of about several μm and dispersion of crystallite size distribution have been evaluated by statistical analysis of spinner-scan diffraction intensity data. The method can be applied to polycrystalline materials and also multi-phase mixtures.

  6. Accurate molecular structures of chlorothiazide and hydrochlorothiazide by joint refinement against powder neutron and X-ray diffraction data.

    Science.gov (United States)

    Leech, Charlotte K; Fabbiani, Francesca P A; Shankland, Kenneth; David, William I F; Ibberson, Richard M

    2008-02-01

    The compounds chlorothiazide and hydrochlorothiazide (crystalline form II) have been studied in their fully hydrogenous forms by powder neutron diffraction on the GEM diffractometer. The results of joint Rietveld refinement of the structures against multi-bank neutron and single-bank X-ray powder data are reported and show that accurate and precise structural information can be obtained from polycrystalline molecular organic materials by this route.

  7. First experiments with a newly developed high-pressure/high-temperature cell for neutron powder diffraction

    International Nuclear Information System (INIS)

    Fuetterer, K.; Depmeier, W.; Strobel, J.; Vogt, T.

    1991-01-01

    On the basis of the well known and widely used piston cylinder high pressure cell of the McWhan type, a new high-pressure/high-temperature cell for angle dispersive neutron powder diffraction has been developed. A pressure/temperature range of simultaneously 1.5 GPa and 500 o C is aimed at. Up to now two test experiments with the cell on D2B of the ILL with calcite as sample could be performed. The maximum, non simultaneous pressures and temperatures reached so far, amount to about 0.75 GPa and 400 o C, respectively. The characteristics of the cell construction and first experimental experiences and results are reported. (author) 3 figs., 1 tab., 10 refs

  8. Crystal structure refinement of Cu6O8YCl by powder neutron diffraction

    International Nuclear Information System (INIS)

    Kawashima, Kenji; Akimitsu, Jun; Horigane, Kazumasa; Ohoyama, Kenji

    2012-01-01

    We report the crystal structure parameters of clathrate-type copper-oxide Cu 6 O 8 YCl, which belongs to the Cu 6 O 8 MX (M = cation, X = anion) family, investigated by the powder neutron diffraction technique and the Rietveld method. The crystal structure of Cu 6 O 8 YCl was identified to be a cubic structure with the space group Fm3-bar m. The Cl atom is located at the 4a site, which is the center position of the Cu 6 O 8 cage, and the Y atom occupies the 4b site in the cuboid space. The Y and Cl atoms have anomalously large atomic displacement parameters (U iso ) at room temperature, which suggests that Y and Cl atoms respectively present in a cuboid and in a Cu 6 O 8 cage exhibit intensive motion such as rattling, as recently observed for clathrate compounds.

  9. Structure analysis of K3H(SO4)2 by neutron powder diffraction

    International Nuclear Information System (INIS)

    Murakami, Satoshi; Kuroiwa, Yoshihiro; Noda, Yukio; Nakai, Yusuke; Kamiyama, Takashi; Asano, Hajime.

    1993-01-01

    Neutron powder diffraction experiments of K 3 H(SO 4 ) 2 were carried out at KENS-HRP station in order to obtain the positional parameters of hydrogen nuclei. The data was taken at six different temperatures from room temperature to 20K. Even though K 3 H(SO 4 ) 2 contained a hydrogen atom, the structural analysis was successfully performed by using a program RIETAN. Concerning the hydrogen position, four different models give almost the same R-factor so that the state of the hydrogen nucleus is not uniquely determined. The result based on the assumption that a hydrogen nucleus occupies two sites shows that the distance of split hydrogen nuclei is shorter than the distance of hydrogen electron clouds. This result suggests that a large polarizability exists in a hydrogen atom. (author)

  10. Neutron powder diffraction for complex magnetic structures - some examples from research in uranium intermetallics

    International Nuclear Information System (INIS)

    Robinson, R.A.

    2000-01-01

    Full text: Since its inception after the second-world war, neutron scattering has been the method of choice for solving magnetic structures. I will review the type of information that one can extract from neutron powder diffraction with modern low- and high-resolution instruments, and the use and misuse of Rietveld refinement methods. It is essential to understand and use the polarisation dependence of the magnetic cross-section, whose systematic-absence rules are more complicated than those in the standard crystallography tables, and it is also often beneficial to use symmetry arguments based on Shubnikov groups or irreducible representations. To illustrate these ideas, the specific cases of the noncollinear antiferromagnets UPdSn, U 2 Pd 2 Sn and U 2 Pd 2 In will be discussed

  11. Characterization of polymorphic solid-state changes using variable temperature X-ray powder diffraction

    DEFF Research Database (Denmark)

    Karjalainen, Milja; Airaksinen, Sari; Rantanen, Jukka

    2005-01-01

    The aim of this study was to use variable temperature X-ray powder diffraction (VT-XRPD) to understand the solid-state changes in the pharmaceutical materials during heating. The model compounds studied were sulfathiazole, theophylline and nitrofurantoin. This study showed that the polymorph form...... of sulfathiazole SUTHAZ01 was very stable and SUTHAZ02 changed as a function of temperature to SUTHAZ01. Theophylline monohydrate changed via its metastable form to its anhydrous form during heating and nitrofurantoin monohydrate changed via amorphous form to its anhydrous form during heating. The crystallinity...... of SUTHAZ01, SUTHAZ02 and theophylline monohydrate were very high and stable. Nitrofurantoin monohydrate was also very crystalline at room temperature but during heating at lower temperatures the crystallinity decreased and started to increase strongly at the temperature where the sample had changed...

  12. Identification of ancient textile fibres from Khirbet Qumran caves using synchrotron radiation microbeam diffraction

    International Nuclear Information System (INIS)

    Mueller, Martin; Murphy, Bridget; Burghammer, Manfred; Riekel, Christian; Roberts, Mark; Papiz, Miroslav; Clarke, David; Gunneweg, Jan; Pantos, Emmanuel

    2004-01-01

    Archaeological textiles fragments from the caves of Qumran in the Dead Sea region were investigated by means of X-ray microbeam diffraction on single fibres. This non-destructive technique made the identification of the used plant textile fibres possible. Apart from bast fibres (mainly flax), cotton was identified which was most unexpected in the archaeological context

  13. Synchrotron Radial X-ray Diffraction Studies of Deformation of Polycrystalline MgO

    Science.gov (United States)

    Girard, J.; Tsujino, N.; Mohiuddin, A.; Karato, S. I.

    2016-12-01

    X-ray diffraction analyses have been used for decades to study mechanical properties of polycrystalline samples during in-situ high-pressure deformation. When polycrystalline materials are deformed, stresses develop in grains and lead to lattice distortion. Using X-ray diffraction we can estimate the lattice strain for each (hkl) diffraction plans and calculate the applied stress for each (hkl), using [Singh, 1993] relation. However, this method doesn't take into account plastic anisotropy. As a results of plastic anisotropy present in the material, stress estimated from this method can be largely differ depending on (hkl) diffraction planes [Karato, 2009]. Studying the stress estimate for each (hkl) plane, might help us distinguish dominant deformation mechanisms activated during deformation such as diffusion (we will observe small stress variation as a function of (hkl) diffraction planes) or dislocation creep (we will observe a stress variation as a function of (hkl) diffraction planes that could also give us clues on potential slip system activity). In this study we observed stress evolution in MgO polycrystalline samples deformed under mantle pressure and temperature for (200) and (220) diffraction planes. Using a range MgO grain sizes we were able to control the active deformation mechanism (for e.g. diffusion creep or dislocation creep). For coarse-grained specimens, we observed strong (hkl) dependence of radial strain indicating the operation of dislocation creep. The observed (hkl) dependence changes with pressure suggesting a change in the slip system: at pressures higher than 27 GPa, (200) shows larger stress estimate than (220). In contrast, at lower pressures, (220) shows larger stress estimate than (200). This might indicate a slip system transition in MgO occurring under lower mantle conditions. From {110} plane to {100} plane. This is in good agreement with theoretical predictions and numerical calculation [Amodeo et al., 2012] and has an important

  14. High-pressure powder neutron diffraction study on lead scandium niobate.

    Science.gov (United States)

    Maier, B J; Angel, R J; Mihailova, B; Marshall, W G; Gospodinov, M; Bismayer, U

    2011-01-26

    The structural evolution of PbSc(0.5)Nb(0.5)O(3) (PSN) under pressure has been studied by in situ powder neutron diffraction. Rietveld refinements to the data show that the continuous phase transition detected by x-ray diffraction at p(c) = 4.1 GPa (Maier et al 2010 Phys. Rev. B 81 174116) is associated with long-range ordering of antiphase octahedral tilts and local ordering of ferroic Pb displacements. Similar to PbSc(0.5)Ta(0.5)O(3) (PST) (Maier et al 2010 Acta Crystallogr. 66 280-91), antiphase octahedral tilting even exists below the critical pressure in a regime in which the structure retains a cubic metric. In contrast to PST, in which the Pb atomic displacement parameters (DPs) form ellipsoids elongated along the cubic {111} directions, the atomic DPs of Pb in PSN form flattened discs parallel to the cubic {111}-planes. This indicates that in PST the Pb displacements are along the cubic {111} directions, whereas in PSN the local Pb displacements are randomly distributed along the cubic {110} directions. The latter can be explained by the abundance of underbonded oxygen atoms associated with the chemical B-site disorder.

  15. In Situ Powder Diffraction Studies of Electrode Materials in Rechargeable Batteries.

    Science.gov (United States)

    Sharma, Neeraj; Pang, Wei Kong; Guo, Zaiping; Peterson, Vanessa K

    2015-09-07

    The ability to directly track the charge carrier in a battery as it inserts/extracts from an electrode during charge/discharge provides unparalleled insight for researchers into the working mechanism of the device. This crystallographic-electrochemical information can be used to design new materials or modify electrochemical conditions to improve battery performance characteristics, such as lifetime. Critical to collecting operando data used to obtain such information in situ while a battery functions are X-ray and neutron diffractometers with sufficient spatial and temporal resolution to capture complex and subtle structural changes. The number of operando battery experiments has dramatically increased in recent years, particularly those involving neutron powder diffraction. Herein, the importance of structure-property relationships to understanding battery function, why in situ experimentation is critical to this, and the types of experiments and electrochemical cells required to obtain such information are described. For each battery type, selected research that showcases the power of in situ and operando diffraction experiments to understand battery function is highlighted and future opportunities for such experiments are discussed. The intention is to encourage researchers to use in situ and operando techniques and to provide a concise overview of this area of research. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  16. Hydration process for calcium-aluminate cement within EVA emulsion by SPring-8 synchrotron radiation x-ray diffraction method

    International Nuclear Information System (INIS)

    Kotera, Masaru; Matsuda, Ikuyo; Miyashita, Keiko; Adachi, Nobuyuki; Tamura, Hisayuki

    2005-01-01

    Polymer-modified mortars which consist of a polymer emulsion and cement materials have been widely developed in the construction materials fields. Forming process of the polymer-modified cement membrane simultaneously involves evaporation of water within the polymer emulsion and hydration of cement. It is important for the polymer-modified cement paste that the hydrate crystal of cement is generating by the hydration during the setting process under existence of the polymer emulsion. In this study, hydration process for calcium-aluminate cement under existence of poly (ethylene-vinyl acetate) (EVA) emulsion (polymer-cement ratio=100%) was investigated by X-ray diffraction method using synchrotron radiation (SPring-8). The diffraction peaks of calcium aluminate (CA) disappeared after the hardening, on the other hand, the peaks of hydrate crystals of calcium-aluminate cement (C 2 AH 8 and C 3 AH 6 ) could be observed. This polymer-modified cement paste hydrated using the water within the polymer emulsion. The hydration of C 2 AH 8 from CA started at around 300 min, and then C 3 AH 6 hydrate crystal increased after 700 min at ambient temperature. This implies that the conversion from C 2 AH 8 to C 3 AH 6 occurred to be more stable phase. The setting temperature affected the reaction rate. In case of hydration at 35degC, the start time of the hydration for calcium-aluminate cement was quicker than that in the ambient temperature four or more times. (author)

  17. In Situ Neutron and Synchrotron X-ray Diffraction Studies of Jarosite at High-Temperature High-Pressure Conditions

    Science.gov (United States)

    Xu, H.; Zhao, Y.; Hickmott, D.; Zhang, J.; Vogel, S.; Daemen, L.; Hartl, M.

    2011-03-01

    Jarosite (KFe 3 (SO4)2 (OH)6) occurs in acid mine drainage and epithermal environments and hot springs associated with volcanic activity. Jarosite is also of industrial interest as an iron-impurity extractor from zinc sulfide ores. In 2004, jarosite was detected by the Mars Exploration Rover Mössbauer spectrometer, which has been interpreted as a strong evidence for the existence of water (and possibly life) on ancient Mars. This discovery has spurred considerable interests in stability and structural behavior of jarosite and related phases at various temperature, pressure, and aqueous conditions. In this work, we have investigated the crystal structure and phase stability of jarosite at temperatures up to 900 K and/or pressures up to 9 GPa using in situ neutron and synchrotron X-ray diffraction. To avoid the large incoherent scattering of neutrons by hydrogen, a deuterated sample was synthesized and characterized. Rietveld analysis of the obtained diffraction data allowed determination of unit-cell parameters, atomic positions and atomic displacement parameters as a function of temperature and pressure. In addition, the coefficients of thermal expansion, bulk moduli and pressure-temperature stability regions of jarosite were determined.

  18. PRELIMINARY RESULTS IN SYNCHROTRON X-RAY DIFFRACTION MEASUREMENTS OF RUBBER COMPOSITES STRUCTURE BEFORE AND AFTER EXPOSURE TO HYDROGEN

    Directory of Open Access Journals (Sweden)

    Francesca Cosmi

    2011-05-01

    Full Text Available In future years, fuel cells are expected to represent a promising technology as a source of heat and electricity in buildings and of electrical power for vehicles, since fossil fuels are exhausting and significantly degrade air quality. It is well known that, when exposed to a hydrogen environment, hydrogen embrittlerment may affect materials such as iron and steel. But these are not the only materials that are used for hydrogen equipment. In particular, the rubber materials used for O–rings that seal high pressure hydrogen gas equipment show problems of internal fracture, called blister fracture, when the gas is rapidly decompressed. As many different kinds of fillers can be used, in this work we started to investigate the influence of the type of filler on the rubber composites structure, by means of X-ray diffraction measurements performed at the Elettra synchrotron radiation facility in Trieste. In this preliminary study, three kinds of samples were analyzed before and after exposure to hydrogen: Sulphur vulcanized EPDM, Peroxide vulcanized EPDM and Sulphur vulcanized NBR. While Peroxide vulcanized samples did not show significant differences in the diffraction pattern, changes could be detected in the cristalline form of Sulfure vulcanized rubber.

  19. In situ laser heating and radial synchrotron X-ray diffraction ina diamond anvil cell

    Energy Technology Data Exchange (ETDEWEB)

    Kunz, Martin; Caldwell, Wendel A.; Miyagi, Lowell; Wenk,Hans-Rudolf

    2007-06-29

    We report a first combination of diamond anvil cell radialx-ray diffraction with in situ laser heating. The laser-heating setup ofALS beamline 12.2.2 was modified to allow one-sided heating of a samplein a diamond anvil cell with an 80 W yttrium lithium fluoride laser whileprobing the sample with radial x-ray diffraction. The diamond anvil cellis placed with its compressional axis vertical, and perpendicular to thebeam. The laser beam is focused onto the sample from the top while thesample is probed with hard x-rays through an x-ray transparentboron-epoxy gasket. The temperature response of preferred orientation of(Fe,Mg)O is probed as a test experiment. Recrystallization was observedabove 1500 K, accompanied by a decrease in stress.

  20. Synchrotron Bragg diffraction imaging characterization of synthetic diamond crystals for optical and electronic power device applications.

    Science.gov (United States)

    Tran Thi, Thu Nhi; Morse, J; Caliste, D; Fernandez, B; Eon, D; Härtwig, J; Barbay, C; Mer-Calfati, C; Tranchant, N; Arnault, J C; Lafford, T A; Baruchel, J

    2017-04-01

    Bragg diffraction imaging enables the quality of synthetic single-crystal diamond substrates and their overgrown, mostly doped, diamond layers to be characterized. This is very important for improving diamond-based devices produced for X-ray optics and power electronics applications. The usual first step for this characterization is white-beam X-ray diffraction topography, which is a simple and fast method to identify the extended defects (dislocations, growth sectors, boundaries, stacking faults, overall curvature etc. ) within the crystal. This allows easy and quick comparison of the crystal quality of diamond plates available from various commercial suppliers. When needed, rocking curve imaging (RCI) is also employed, which is the quantitative counterpart of monochromatic Bragg diffraction imaging. RCI enables the local determination of both the effective misorientation, which results from lattice parameter variation and the local lattice tilt, and the local Bragg position. Maps derived from these parameters are used to measure the magnitude of the distortions associated with polishing damage and the depth of this damage within the volume of the crystal. For overgrown layers, these maps also reveal the distortion induced by the incorporation of impurities such as boron, or the lattice parameter variations associated with the presence of growth-incorporated nitrogen. These techniques are described, and their capabilities for studying the quality of diamond substrates and overgrown layers, and the surface damage caused by mechanical polishing, are illustrated by examples.

  1. Use of neutron and synchrotron X-ray diffraction for evaluation of residual stresses in a 2024-T351 aluminum alloy variable-polarity plasma-arc weld

    Science.gov (United States)

    Ganguly, S.; Fitzpatrick, M. E.; Edwards, L.

    2006-02-01

    The residual stress fields associated with variable-polarity plasma-arc (VPPA) welds in 2024-T351 aluminum alloy plates have been measured nondestructively using neutron and synchrotron X-ray diffraction. Neutron diffraction allows in-depth measurements of the full strain tensor to be made in thick components; synchrotron X-rays allow for rapid measurements of strains inside components, although their penetration is less than that of the neutrons and constraints arising from the diffraction geometry generally lead to only two strain components being easily measurable. Hence, a combination of the two techniques, applied as described herein, is ideal for a detailed nondestructive evaluation of residual stresses in plates. The residual stresses in a 12-mm-thick VPPA-welded aluminum 2024-T351 alloy plate have been measured using neutron diffraction. The stresses were then remeasured by a combination of neutron and synchrotron X-ray diffraction after the plate had been reduced in thickness (or, skimmed) to 7 mm by machining both sides of the weld, mimicking the likely manufacturing operation, should such welds be used in aerospace structures. A strong tensile residual stress field was measured in the longitudinal direction, parallel to the weld, in both the as-welded and skimmed specimens. There was only a slight modification of the residual stress state on skimming.

  2. Instability of cyclic superelastic deformation of NiTi investigated by synchrotron X-ray diffraction

    Czech Academy of Sciences Publication Activity Database

    Sedmák, P.; Šittner, Petr; Pilch, Jan; Curfs, C.

    2015-01-01

    Roč. 94, Aug (2015), s. 257-270 ISSN 1359-6454 R&D Projects: GA ČR GB14-36566G; GA ČR GPP108/12/P111; GA ČR GA14-15264S; GA ČR GAP107/12/0800 Institutional support: RVO:68378271 Keywords : shape memory alloy * NiTi * superelasticity * cyclic deformation * in situ X-ray diffraction Subject RIV: JG - Metallurgy Impact factor: 5.058, year: 2015

  3. Crystal structure and tautomerism of Pigment Yellow 138 determined by X-ray powder diffraction and solid-state NMR

    DEFF Research Database (Denmark)

    Gumbert, Silke D.; Körbitzer, Meike; Alig, Edith

    2016-01-01

    The crystal structure of C.I. Pigment Yellow 138 was determined from X-ray powder diffraction data using real-space methods with subsequent Rietveld refinements. The tautomeric state was investigated by solid-state 1D and 2D multinuclear NMR experiments. In the crystals, the compound exhibits...... is not a packing effect, but caused by intramolecular steric hindrance....

  4. Validation of molecular crystal structures from powder diffraction data with dispersion-corrected density functional theory (DFT-D)

    DEFF Research Database (Denmark)

    van de Streek, Jacco; Neumann, Marcus A

    2014-01-01

    In 2010 we energy-minimized 225 high-quality single-crystal (SX) structures with dispersion-corrected density functional theory (DFT-D) to establish a quantitative benchmark. For the current paper, 215 organic crystal structures determined from X-ray powder diffraction (XRPD) data and published...

  5. Highly efficient Ru/MnO2 nano-catalysts for Li-O2 batteries: Quantitative analysis of catalytic Li2O2 decomposition by operando synchrotron X-ray diffraction

    Science.gov (United States)

    Liu, Jia; Ma, Yue; Roberts, Matthew; Gustafsson, Torbjörn; Edström, Kristina; Zhu, Jiefang

    2017-06-01

    In-situ or operando quantitative analysis is very important for Li-O2 batteries, in order to properly, accurately and comprehensively evaluate electrocatalysts and characterize Li-O2 electrochemistry in real-time. Synchrotron XRD can provide much higher X-ray intensity and time resolution than traditional in-house diffractometers, and therefore can contribute to quantitative analysis for Li-O2 batteries. Here, operando synchrotron XRD is further developed to quantitatively study Li-O2 batteries with nano-catalysts, Ru/MnO2. The time-resolved oxygen evolution reaction (OER) kinetics for Li-O2 cells with Ru/MNT was systematically investigated using operando synchrotron radiation powder X-ray diffraction (SR-PXD). Li2O2 decomposition in the electrodes with Ru/MNT catalysts during galvanostatic and potentiostatic charge processes followed pseudo-zero-order kinetics and showed ideal Coulombic efficiency (close to 100%). Furthermore, it was found that the OER kinetics for a cell with 2 wt% Ru/MNT charged at a constant potential of 4.3 V was even faster than that for a cell with the same amount of pure Ru nanoparticles, which have been considered as a highly active catalyst for Li-O2 batteries. These results indicated that Ru/MNT with a special nanostructure represented a very efficient electrocatalyst for promoting the OER in Li-O2 batteries. We also demonstrate that synchrotron radiation XRD can "highlight" a way to quantitative analysis for Li-O2 batteries.

  6. In situ neutron diffraction studies of single crystals and powders during microwave irradiation.

    Science.gov (United States)

    Harrison, Andrew; Ibberson, Richard; Robb, Graeme; Whittaker, Gavin; Wilson, Chick; Youngson, Douglas

    2003-01-01

    Microwave dielectric heating has become an important method in chemical synthesis and materials processing over the past 15 years, and in the case of the reactions in solutions, there is a well-developed understanding of heating mechanisms and their influence on reaction rate. In the solid-state however, there is much less clarity, despite the advantages to be gained from better insight into the way in which such electromagnetic radiation may couple directly to charge carriers, accelerating reactions in good conductors. The related issue of the influence of microwave irradiation on biological systems, in particular, proteins, and the way in which this may pose hazards to health is similarly poorly understood despite the obvious relevance this may have to the current debate on the influence of electromagnetic radiation, in particular, microwave transmission, on human health. One reason for the paucity of fundamental insight in both fields is because most work has been performed with microwave equipment whose design is derived from that of a domestic oven, and which is not ideal for in situ studies of microwave driven processes. We have been developing new methods of irradiating a variety of solid samples while measuring structural parameters through a range of diffraction techniques, and describe apparatus that will enable X-ray or neutron scattering measurements to be performed on powders or single crystals under microwave irradiation with controlled power level. We also describe preliminary studies of a single crystal of the molecular solid aspirin, and a powder of the microwave-susceptible ionic material BaTiO3, during microwave irradiation.

  7. An in situ Study of NiTi Powder Sintering Using Neutron Diffraction

    Directory of Open Access Journals (Sweden)

    Gang Chen

    2015-04-01

    Full Text Available This study investigates phase transformation and mechanical properties of porous NiTi alloys using two different powder compacts (i.e., Ni/Ti and Ni/TiH2 by a conventional press-and-sinter means. The compacted powder mixtures were sintered in vacuum at a final temperature of 1373 K. The phase evolution was performed by in situ neutron diffraction upon sintering and cooling. The predominant phase identified in all the produced porous NiTi alloys after being sintered at 1373 K is B2 NiTi phase with the presence of other minor phases. It is found that dehydrogenation of TiH2 significantly affects the sintering behavior and resultant microstructure. In comparison to the Ni/Ti compact, dehydrogenation occurring in the Ni/TiH2 compact leads to less densification, yet higher chemical homogenization, after high temperature sintering but not in the case of low temperature sintering. Moreover, there is a direct evidence of the eutectoid decomposition of NiTi at ca. 847 and 823 K for Ni/Ti and Ni/TiH2, respectively, during furnace cooling. The static and cyclic stress-strain behaviors of the porous NiTi alloys made from the Ni/Ti and Ni/TiH2 compacts were also investigated. As compared with the Ni/Ti sintered samples, the samplessintered from the Ni/TiH2 compact exhibited a much higher porosity, a higher close-to-total porosity, a larger pore size and lower tensile and compressive fracture strength.

  8. Hydride reorientation in Zircaloy-4 examined by in situ synchrotron X-ray diffraction

    Energy Technology Data Exchange (ETDEWEB)

    Weekes, H.E. [Department of Materials, Royal School of Mines, Imperial College London, Prince Consort Road, London SW7 2BP (United Kingdom); Jones, N.G. [Department of Materials Science and Metallurgy, University of Cambridge, 27 Charles Babbage Road, Cambridge CB3 0FS (United Kingdom); Lindley, T.C. [Department of Materials, Royal School of Mines, Imperial College London, Prince Consort Road, London SW7 2BP (United Kingdom); Dye, D., E-mail: david.dye@imperial.ac.uk [Department of Materials, Royal School of Mines, Imperial College London, Prince Consort Road, London SW7 2BP (United Kingdom)

    2016-09-15

    The phenomenon of stress-reorientation has been investigated using in situ X-ray diffraction during the thermomechanical cycling of hydrided Zircaloy-4 tensile specimens. Results have shown that loading along a sample’s transverse direction (TD) leads to a greater degree of hydride reorientation when compared to rolling direction (RD)-aligned samples. The elastic lattice micro-strains associated with radially oriented hydrides have been revealed to be greater than those oriented circumferentially, a consequence of strain accommodation. Evidence of hydride redistribution after cycling, to α-Zr grains oriented in a more favourable orientation when under an applied stress, has also been observed and its behaviour has been found to be highly dependent on the loading axis. Finally, thermomechanical loading across multiple cycles has been shown to reduce the difference in terminal solid solubility of hydrogen during dissolution (TSS{sub D,H}) and precipitation (TSS{sub P,H}).

  9. Single crystal and powder diffraction characterization of three polymorphic forms of Acitretin.

    Science.gov (United States)

    Malpezzi, Luciana; Magnone, Grato Angelo; Masciocchi, Norberto; Sironi, Angelo

    2005-05-01

    Acitretin [all-trans-9-(4-methoxy-2,3,6-trimethylphenyl)-3,7-dimethyl-2,4,6,8-nonatetraenoic acid or 3-methoxy-2-methyl-17-nor-1,2,3,4-tetradehydroretinoic acid], a widely marketed oral synthetic retinoid, introduced for clinical use as effective therapy against psoriasis, was found to crystallize in three polymorphic modifications (hereafter, I, II, and III), the crystal structures of which have been determined by single-crystal diffractometry (form I) or X-ray powder diffraction methods (form II and III) from conventional laboratory data only. In these latter cases, real space techniques (simulated annealing and whole-profile pattern matching) have been employed. Polymorph I crystallizes in space group P2(1), Z = 8, with unit cell parameters a = 7.894(1), b = 58.454(6), c = 8.161(1) angstroms, beta = 102.04(1) degrees, and V = 3682.9(8) angstroms3. Polymorph II crystallizes in space group P2(1)/n, Z = 4, with unit cell parameters a = 13.999(2), b = 10.714(1), c = 12.465(2) angstroms, beta = 98.76(5) degrees, and V = 1847.9(3) angstroms3. Polymorph III crystallizes in space group P2(1)/c, Z = 4, with unit cell parameters a = 3.0751(4), b = 4.0487(4), c = 14.956(2) angstroms, beta = 100.41(7) degrees, and V = 1831.3(4) angstroms3. Polymorph I, found to be identical with that deposited in the European Pharmacopeia, shows four crystallographically independent Acitretin molecules, arranged in pairs through conventional hydrogen-bonded carboxylic dimers; also in form II, carboxylic dimers are observed, located on crystallographic inversion centres, while in form III, a catameric arrangement of the carboxylic residues, winding up about the rather short monoclinic axis, generates one-dimensional chains of hydrogen-bonded Acitretin molecules. Thermal analysis showed that form I can be quantitatively transformed into form II by moderate heating near 200 degrees C, under vacuum. These results show that ab initio structural studies from conventional laboratory X-ray powder

  10. Computer x-ray powder diffraction patterns and densities for corundum, aluminium, zirconium, delta-UZr2 and the zirconium hydrides

    International Nuclear Information System (INIS)

    Ferguson, I.F.

    1976-11-01

    The computer-calculated X-ray powder diffraction patterns and theoretical densities of α-Al 2 O 3 ; Al; α-Zr; β-Zr; delta-UZr 2 ; γ, delta - and epsilon-zirconium hydrides are presented. Brief comments are given on some of the published X-ray powder diffraction data on these phases. (author)

  11. Development of a silicon microstrip detector with single photon sensitivity for fast dynamic diffraction experiments at a synchrotron radiation beam

    Science.gov (United States)

    Arakcheev, A.; Aulchenko, V.; Kudashkin, D.; Shekhtman, L.; Tolochko, B.; Zhulanov, V.

    2017-06-01

    Time-resolved experiments on the diffraction of synchrotron radiation (SR) from crystalline materials provide information on the evolution of a material structure after a heat, electron beam or plasma interaction with a sample under study. Changes in the material structure happen within a microsecond scale and a detector with corresponding parameters is needed. The SR channel 8 of the VEPP-4M storage ring provides radiation from the 7-pole wiggler that allows to reach several tens photons within one μs from a tungsten crystal for the most intensive diffraction peak. In order to perform experiments that allow to measure the evolution of tungsten crystalline structure under the impact of powerful laser beam, a new detector is developed, that can provide information about the distribution of a scattered SR flux in space and its evolution in time at a microsecond scale. The detector is based on the silicon p-in-n microstrip sensor with DC-coupled metal strips. The sensor contains 1024 30 mm long strips with a 50 μm pitch. 64 strips are bonded to the front-end electronics based on APC128 ASICs. The APC128 ASIC contains 128 channels that consist of a low noise integrator with 32 analogue memory cells each. The integrator equivalent noise charge is about 2000 electrons and thus the signal from individual photons with energy above 40 keV can be observed. The signal can be stored at the analogue memory with 10 MHz rate. The first measurements with the beam scattered from a tungsten crystal with energy near 60 keV demonstrated the capability of this prototype to observe the spatial distribution of the photon flux with the intensity from below one photon per channel up to 0~10 photons per channel with a frame rate from 10 kHz up to 1 MHz.

  12. Determining the Structure of Biomaterials Interfaces using Synchrotron-based X-ray Diffraction

    Energy Technology Data Exchange (ETDEWEB)

    McBride, M

    2002-01-24

    The purpose of this project is to explore the feasibility of using surface X-ray diffraction (SXRD) to determine the structure of biomineral surfaces in electrolyte solutions and of the adsorbed layer of acidic amino acids that are believed to play a central role in the control of biomineral formation and function. The work is a critical component in the development of an integrated picture of the physical and chemical basis for deposition and dissolution at solid-liquid interfaces in biological systems, and brings a new and very powerful surface-sensitive capability to LLNL. We have chosen as our model systems calcium carbonate and calcium phosphate in aspartic and glutamic acid-bearing solutions. The calcium compounds are ubiquitous among biomineral structures, both those that are beneficial such as bones and teeth, and those that are pathological such as kidney stones, while the two acidic amino acids--both as simple and poly-amino acids--are the dominant constituents of protein mixtures implicated in the control of biomineralization. The goals of the work are: (1) to determine the surface structure of pure calcium phosphate and calcium carbonate surfaces in aqueous solution using SXRD; (2) to determine how those surfaces are modified by the presence of aspartic and glutamic acid, both as the simple amino acids and as poly-aspartate and poly-glutamate and (3) to model the interactions of acidic amino acids with calcite.

  13. Neutron powder diffraction and molecular dynamics study of superionic SrBr2

    International Nuclear Information System (INIS)

    Hull, S; Norberg, S T; Eriksson, S G; Mohn, C E

    2013-01-01

    The nature of the dynamic ionic disorder within the high-temperature superionic phase of strontium bromide, β-SrBr 2 , has been investigated using reverse Monte Carlo (RMC) modelling of neutron powder diffraction data and complementary ab initio molecular dynamics (MD) simulations. The RMC and MD results are in good agreement and indicate the presence of extensive dynamic disorder within the Br − sublattice of the cubic fluorite structure. Rapid anion diffusion predominantly occurs as hops between nearest neighbour sites in the 〈100〉 directions, though the trajectories are markedly curved and pass through the peripheries of the octahedral voids in the cation sublattice. In addition, there are extensive correlations between the motions of individual Br − , often leading to the formation of a short-lived square antiprism co-ordination environment around the Sr 2+ . Such polyhedra are observed within the (ambient temperature) ordered tetragonal crystal structure of α-SrBr 2 . The nature of the ionic disorder in SrBr 2 is of particular interest because it is the only known example of a Br − -ion superionic. Owing to the large size of this anion, a comparison with the behaviour of other superionic phases gives an insight into the role of ionic size on the conducting properties within these materials. (paper)

  14. Versatile in situ powder X-ray diffraction cells for solid-gas investigations

    Energy Technology Data Exchange (ETDEWEB)

    Jensen, Torben R.; Nielsen, Thomas K.; Joergensen, Jens-Erik [Aarhus Univ. (Denmark). Center for Energy Materials, Center for Materials Crystallography; Filinchuk, Yaroslav [European Synchrotron Radiation Facility, Grenoble (France). Swiss-Norwegian Beam Lines; Cerenius, Yngve [Lund Univ. (Sweden). MAX-lab; Gray, Evan MacA.; Webb, Colin J. [Griffith Univ., Nathan, Brisbane (Australia). Queensland Micro- and Nanotechnology Centre

    2010-12-15

    This paper describes new sample cells and techniques for in situ powder X-ray diffraction specifically designed for gas absorption studies up to ca 300 bar (1 bar = 100 000 Pa) gas pressure. The cells are for multipurpose use, in particular the study of solid-gas reactions in dosing or flow mode, but can also handle samples involved in solid-liquid-gas studies. The sample can be loaded into a single-crystal sapphire (Al{sub 2}O{sub 3}) capillary, or a quartz (SiO{sub 2}) capillary closed at one end. The advantages of a sapphire single-crystal cell with regard to rapid pressure cycling are discussed, and burst pressures are calculated and measured to be {proportional_to}300 bar. An alternative and simpler cell based on a thin-walled silicate or quartz glass capillary, connected to a gas source via a VCR fitting, enables studies up to {proportional_to}100 bar. Advantages of the two cell types are compared and their applications are illustrated by case studies. (orig.)

  15. Versatile in situ powder X-ray diffraction cells for solid-gas investigations

    International Nuclear Information System (INIS)

    Jensen, Torben R.; Nielsen, Thomas K.; Joergensen, Jens-Erik; Filinchuk, Yaroslav; Cerenius, Yngve; Gray, Evan MacA.; Webb, Colin J.

    2010-01-01

    This paper describes new sample cells and techniques for in situ powder X-ray diffraction specifically designed for gas absorption studies up to ca 300 bar (1 bar = 100 000 Pa) gas pressure. The cells are for multipurpose use, in particular the study of solid-gas reactions in dosing or flow mode, but can also handle samples involved in solid-liquid-gas studies. The sample can be loaded into a single-crystal sapphire (Al 2 O 3 ) capillary, or a quartz (SiO 2 ) capillary closed at one end. The advantages of a sapphire single-crystal cell with regard to rapid pressure cycling are discussed, and burst pressures are calculated and measured to be ∝300 bar. An alternative and simpler cell based on a thin-walled silicate or quartz glass capillary, connected to a gas source via a VCR fitting, enables studies up to ∝100 bar. Advantages of the two cell types are compared and their applications are illustrated by case studies. (orig.)

  16. Correlating cycling history with structural evolution in commercial 26650 batteries using in operando neutron powder diffraction

    Science.gov (United States)

    Goonetilleke, Damian; Pramudita, James C.; Hagan, Mackenzie; Al Bahri, Othman K.; Pang, Wei Kong; Peterson, Vanessa K.; Groot, Jens; Berg, Helena; Sharma, Neeraj

    2017-03-01

    Ex situ and time-resolved in operando neutron powder diffraction (NPD) has been used to study the structural evolution of the graphite negative electrode and LiFePO4 positive electrode within ANR26650M1A commercial batteries from A123 Systems, in what to our knowledge is the first reported NPD study investigating a 26650-type battery. Batteries with different and accurately-known electrochemical and storage histories were studied, enabling the tell-tale signs of battery degradation to be elucidated using NPD. The ex-situ NPD data revealed that the intensity of the graphite/lithiated graphite (LixC6 or LiyC) reflections was affected by battery history, with lower lithiated graphite (LiC12) reflection intensities typically corresponding to more abused batteries. This indicates that the lithiation of graphite is less progressed in more abused batteries, and hence these batteries have lower capacities. In operando NPD allows the rate of structural evolution in the battery electrode materials to be correlated to the applied current. Interestingly, the electrodes exhibit different responses to the applied current that depend on the battery cycling history, with this particularly evident for the negative electrode. Therefore, this work illustrates how NPD can be used to correlate a battery history with electrode structure.

  17. Neutron powder diffraction and molecular dynamics study of superionic SrBr2

    Science.gov (United States)

    Hull, S.; Norberg, S. T.; Eriksson, S. G.; Mohn, C. E.

    2013-11-01

    The nature of the dynamic ionic disorder within the high-temperature superionic phase of strontium bromide, β-SrBr2, has been investigated using reverse Monte Carlo (RMC) modelling of neutron powder diffraction data and complementary ab initio molecular dynamics (MD) simulations. The RMC and MD results are in good agreement and indicate the presence of extensive dynamic disorder within the Br- sublattice of the cubic fluorite structure. Rapid anion diffusion predominantly occurs as hops between nearest neighbour sites in the directions, though the trajectories are markedly curved and pass through the peripheries of the octahedral voids in the cation sublattice. In addition, there are extensive correlations between the motions of individual Br-, often leading to the formation of a short-lived square antiprism co-ordination environment around the Sr2+. Such polyhedra are observed within the (ambient temperature) ordered tetragonal crystal structure of α-SrBr2. The nature of the ionic disorder in SrBr2 is of particular interest because it is the only known example of a Br--ion superionic. Owing to the large size of this anion, a comparison with the behaviour of other superionic phases gives an insight into the role of ionic size on the conducting properties within these materials.

  18. X-ray Powder Diffraction for Characterization of Raw Materials in Banknotes.

    Science.gov (United States)

    Marabello, Domenica; Benzi, Paola; Lombardozzi, Antonietta; Strano, Morela

    2017-07-01

    We report about the X-ray powder diffraction characterization of crystalline materials used to produce genuine and counterfeit banknotes, performed with a single-crystal diffractometer that permits fast and nondestructive measurements in different 0.5-mm sized areas; 20-euro denomination genuine banknotes were analyzed, and results were compared with counterfeit banknotes. The analysis shows that the papers used to print real banknotes are composed, as expected, of cotton-based cellulose and titanium dioxide as crystalline additive, but different polymorphs of TiO 2 for different emission countries are evidenced. The counterfeit banknotes are composed of cellulose based on wood pulp; moreover, an unexpected significant quantity of TiO 2 was found to be mixed with calcite, indicating that the paper employed by forgers is not simply a common low-cost type. The crystalline index and intensity ratios between the peaks attributable to cellulose and fillers can provide additional information to trace back paper suppliers for forensic purposes. © 2017 American Academy of Forensic Sciences.

  19. FTIR spectroscopy and X-ray powder diffraction characterization of microcrystalline cellulose obtained from alfa fibers

    Directory of Open Access Journals (Sweden)

    Trache D.

    2013-07-01

    Full Text Available Many cereal straws have been used as raw materials for the preparation of microcrystalline cellulose (MCC. These raw materials were gradually replaced with wood products; nevertheless about 10% of the world overall pulp production is obtained from non-wood raw material. The main interest in pulp made from straw is that it provides excellent fibres for different industries with special properties, and that it is the major available source of fibrous raw material in some geographical areas. The aim of the present work was to characterize microcrystalline cellulose prepared from alfa fibers using the hydrolysis process. The products obtained are characterized with FTIR spectroscopy and X-ray powder diffraction. As a result, FTIR spectroscopy is an appropriate technique for studying changes occurred by any chemical treatment. The spectrum of alfa grass stems shows the presence of lignin and hemicelluloses. However, the cellulose spectrum indicates that the extraction of lignin and hemicellulose was effective. The X-ray analysis indicates that the microcrystalline cellulose is more crystalline than the source material.

  20. Synchrotron X-ray diffraction studies of phase transitions in physisorbed monolayers of rare gases on graphite

    International Nuclear Information System (INIS)

    Bohr, J.

    1984-01-01

    This study is an investigation of phase transition in monoatomic layers adsorbed on graphite. Such effects can be considered physical realizations of two-dimensional systems. The experimental technique used is synchrotron X-ray diffraction. Systems which have been investigated include the commensurate-incommensurate phase transition in krypton monolayer. By adjusting the spreading pressure in the krypton layer by means of a coadsorbent deuterium gas it has been unambiguously demonstrated that at low temperatures the phase transition is of first order. A melting study of incommensurate argon monolayers demonstrates an experimental verification of the possibility for having a continuous melting transition in two-dimensions. Mixtures of two-components have been investigated for their phases. No (chemical) order-disorder transition is seen. A discussion is given on this lack of a chemical order. This lack is utilized to study the commensurate-incommensurate phase transition driven by average particle size. Finally, a special low-temperature phase is identified in a xenon monlayer which is diluted with freon. (Auth.)

  1. P3HT/PCBM polymer thin films studied by synchrotron-based grazing incidence X-ray diffraction

    International Nuclear Information System (INIS)

    Yang Yingguo; Zhengguan Haojie; Ji Gengwu; Feng Shanglei; Li Xiaolong; Gao Xingyu

    2014-01-01

    Background: The microstructures of P3HT (poly(3-hexyl-thiophene)) in P3HT/PCBM ([6, 6]-phenyl C61-butyric acid methyl ester) thin films play a key role in governing the performance of organic solar cells (OSCs) based on these films. Purpose: We aim to study the self-organization of P3HT in the P3HT/PCBM thin films annealed at different temperatures. Methods: Using different incidence angles, information about the microstructures of P3HT at different depths in these films was obtained by synchrotron based grazing incidence X-ray diffraction (GIXRD). Results: It is shown that the crystalline structure of P3HT has been substantially improved by thermal annealing. One dimensional GIXRD clearly indicates that P3HT edge-on structures in the inner layers have been improved with their number increased in comparison with those at the surface and the interface layers. In addition, thermal annealing also helps the formation of P3HT face-on structures in the films, as evidenced by 2 dimensional GIXRD. Conclusion: The improved structures in these films lead to more charge transport channels formed to improve the carrier mobility, which in turn helps the improvement of OSCs. Thus, the present GIXRD results will improve the understanding of annealing effects at different depths of the P3HT/PCBM thin films for enhanced OSCs devices. (authors)

  2. Analysis of residual stress in metal-inert-gas-welded Al-2024 using neutron and synchrotron X-ray diffraction

    International Nuclear Information System (INIS)

    Ganguly, S.; Stelmukh, V.; Edwards, L.; Fitzpatrick, M.E.

    2008-01-01

    A combination of neutron and synchrotron X-ray diffraction was used to measure and map the full three-dimensional state of residual stress across the cross-section in coupon samples of metal-inert-gas (MIG)-welded 2024 aluminium alloy. Samples were analysed both as-welded and following a post-welding skim which served to remove the weld flash and reduce the plate thickness. The profile of the residual stress and its evolution following skimming has been accurately characterized. The longitudinal direction shows the highest residual stress, approaching 300 MPa in tension. The skimming treatment did not change the peak stress, but the overall profile of stress was altered: this is slightly unexpected as machining away stressed material would generally be expected to reduce the peak residual stress. The results are discussed in terms of the generation of stress during welding and its evolution during skimming. Finally a comparison is made with the stress generated in the as-welded and skimmed conditions of a variable polarity plasma arc (VPPA)-welded specimen of similar dimensions, to show the effects of different weld processes on the residual stress generated. The stress measurement in the VPPA sample was carried out under near identical experimental conditions

  3. Experimental determination of bulk modulus of 14Å tobermorite using high pressure synchrotron X-ray diffraction

    KAUST Repository

    Oh, Jae Eun

    2012-02-01

    Using a diamond anvil cell, 14 Å tobermorite, a structural analogue of calcium silicate hydrates (C-S-H), was examined by high-pressure synchrotron X-ray diffraction up to 4.8 GPa under hydrostatic conditions. The bulk modulus of 14 Å tobermorite was calculated, K o = 47 GPa. Comparison of the current results with previous high pressure studies on C-S-H(I) indicates that: (1) the compression behavior of the lattice parameters a and b of 14 Å tobermorite and C-S-H(I) are very similar, implying that both materials may have very similar Ca-O layers, and also implying that an introduction of structural defects into the Ca-O layers may not substantially change in-plane incompressibility of the ab plane of 14 Å tobermorite; and (2) the bulk modulus values of 14 Å tobermorite and C-S-H(I) are dominated by the incompressibility of the lattice parameter c, which is directly related to the interlayer spacing composed of dreierketten silicate chains, interlayer Ca, and water molecules. © 2011 Elsevier Ltd. All rights reserved.

  4. In situ synchrotron radiation X-ray diffraction studies on molecular aggregation structure of nylon 12 films during bulge testing.

    Science.gov (United States)

    Kojio, Ken; Nagano, Chigusa; Fujimoto, Aya; Nozaki, Shuhei; Yokomachi, Kazutoshi; Kamitani, Kazutaka; Watanabe, Hirohmi; Takahara, Atsushi

    2018-02-28

    It is desirable to establish a method for evaluating mechanical properties, such as modulus and strength, of micrometer and sub-micrometer thick polymer films. Bulge tests, where bulge deformation is imposed on films by the pressure of an inert gas, are suitable for satisfying this demand. However, very few studies on polymer films exist in the literature. In this study, bulge testing equipment for in situ synchrotron radiation wide-angle X-ray diffraction (WAXD) measurements is designed and used to study the relationship between the molecular aggregation structure and the mechanical properties of a crystalline nylon 12 (Ny12) film during bulge testing. Isothermally crystallized and quenched Ny12 films exhibited stress-strain curves similar to those obtained by conventional uniaxial elongation. In situ WAXD measurements during bulge testing revealed that the lattice extension of the crystallites is clearly dependent on crystallinity. Concretely, crystallites in the isothermally crystallized film show higher elastic properties than those in the quenched one. The results of the molecular aggregation structure, including the crystal structure and the amorphous chain surrounding the crystallites, of the films during bulge deformation firstly obtained in this study must be useful for designing toughened polymer films.

  5. Synchrotron X-ray diffraction investigation of the anomalous behavior of ice during freezing of aqueous systems.

    Science.gov (United States)

    Varshney, Dushyant B; Elliott, James A; Gatlin, Larry A; Kumar, Satyendra; Suryanarayanan, Raj; Shalaev, Evgenyi Y

    2009-05-07

    Simple aqueous systems, i.e., phosphate-glycine buffers and pure water, were studied at subambient temperatures by X-ray difractometry using a high-intensity synchrotron radiation source at the Advanced Photon Source of Argonne National Laboratory. Complex X-ray diffraction (XRD) patterns, with two or more poorly resolved peaks in place of each of the four diagnostic peaks of hexagonal ice, 100, 002, 101, and 102, referred as "splitting", were observed in the majority of cases. The splitting of up to 0.05 A (d-spacing) was detected for 100, 002, and 101 peaks, whereas 102 peak was less affected. Deformation of the lattice of hexagonal ice, probably due to local stress created on the ice/ice or ice/container interface during water-to-ice transformation, is proposed as a possible mechanism for the observed splitting of XRD peaks. Using molecular modeling, it was estimated that the observed shifts in the peak positions are equivalent to applying a hydrostatic pressure of 2-3 kbars. The splitting can be used to quantify stresses during freezing, which could improve our understanding of the role of water-to-ice transformation on the destabilization of proteins and other biological systems.

  6. Stress-dependent crystal structure of lanthanum strontium cobalt ferrite by in situ synchrotron X-ray diffraction

    Science.gov (United States)

    Geiger, Philipp T.; Khansur, Neamul H.; Riess, Kevin; Martin, Alexander; Hinterstein, Manuel; Webber, Kyle G.

    2018-02-01

    Lanthanum strontium cobalt ferrite La1-xSrxCo1-yFeyO3-δ (LSCF) is one of the most studied mixed ionic-electronic conductor materials due to electrical and transport properties, which are attractive for intermediate temperature solid oxide fuel cells (SOFCs), oxygen permeation membranes, and catalysis. The integration of such materials, however, depends on the thermal as well as mechanical behavior. LSCF exhibits nonlinear hysteresis during compressive stress-strain measurements, marked by a remanent strain and coercive stress, i.e., ferroelasticity. However, the origin of ferroelastic behavior has not been investigated under high compressive stress. This study, therefore, investigates the microscopic origin of stress-induced mechanical behavior in polycrystalline (La0.6Sr0.4)0.95Co0.2Fe0.8O3-δ using in situ synchrotron x-ray diffraction. The data presented here reveals that the strain response originates from the intrinsic lattice strain as well as the extrinsic domain switching strain without any apparent change in crystallographic symmetry. A comparison of the calculated microscopic strain contribution with that of a macroscopic measurement indicates a significant change in the relative contributions of intrinsic and extrinsic strain depending on the applied stress state, i.e., under maximum stress and after unloading. Direct evidence of the microscopic origin of stress-strain response outlined in this paper may assist in guiding materials design with the improved mechanical reliability of SOFCs.

  7. Sample Handling System for in-situ Powder X-ray Diffraction Instruments., Phase I

    Data.gov (United States)

    National Aeronautics and Space Administration — The proposed innovation is a Powder Handling System (PHS) that will deliver powdered samples to in situ planetary XRD instruments and provide unique means of...

  8. Synchrotron X-ray diffraction studies of phase transitions and mechanical properties of nanocrystalline materials at high pressure

    Energy Technology Data Exchange (ETDEWEB)

    Prilliman, Stephen Gerald [Univ. of California, Berkeley, CA (United States)

    2003-01-01

    The behavior of nanocrystals under extreme pressure was investigated using synchrotron x-ray diffraction. A major part of this investigation was the testing of a prototype synchrotron endstation on a bend magnet beamline at the Advanced Light Source for high pressure work using a diamond anvil cell. The experiments conducted and documented here helped to determine issues of efficiency and accuracy that had to be resolved before the construction of a dedicated ''super-bend'' beamline and endstation. The major conclusions were the need for a cryo-cooled monochromator and a fully remote-controllable pressurization system which would decrease the time to change pressure and greatly reduce the error created by the re-placement of the diamond anvil cell after each pressure change. Two very different types of nanocrystal systems were studied, colloidal iron oxide (Fe2O3) and thin film TiN/BN. Iron oxide nanocrystals were found to have a transition from the γ to the α structure at a pressure strongly dependent on the size of the nanocrystals, ranging from 26 GPa for 7.2 nm nanocrystals to 37 GPa for 3.6 nm nanocrystals. All nanocrystals were found to remain in the α structure even after release of pressure. The transition pressure was also found, for a constant size (5.7 nm) to be strongly dependent on the degree of aggregation of the nanocrystals, increasing from 30 GPa for completely dissolved nanocrystals to 45 GPa for strongly aggregated nanocrystals. Furthermore, the x-ray diffraction pattern of the pressure induced α phase demonstrated a decrease in intensity for certain select peaks. Together, these observations were used to make a complete picture of the phase transition in nanocrystalline systems. The size dependence of the transition was interpreted as resulting from the extremely high surface energy of the α phase which would increase the thermodynamic offset and thereby increase the kinetic barrier to transition

  9. Synchrotron X-ray diffraction studies of phase transitions and mechanical properties of nanocrystalline materials at high pressure

    International Nuclear Information System (INIS)

    Prilliman, Gerald Stephen

    2003-01-01

    The behavior of nanocrystals under extreme pressure was investigated using synchrotron x-ray diffraction. A major part of this investigation was the testing of a prototype synchrotron endstation on a bend magnet beamline at the Advanced Light Source for high pressure work using a diamond anvil cell. The experiments conducted and documented here helped to determine issues of efficiency and accuracy that had to be resolved before the construction of a dedicated ''super-bend'' beamline and endstation. The major conclusions were the need for a cryo-cooled monochromator and a fully remote-controllable pressurization system which would decrease the time to change pressure and greatly reduce the error created by the re-placement of the diamond anvil cell after each pressure change. Two very different types of nanocrystal systems were studied, colloidal iron oxide (Fe 2 O 3 ) and thin film TiN/BN. Iron oxide nanocrystals were found to have a transition from the γ to the α structure at a pressure strongly dependent on the size of the nanocrystals, ranging from 26 GPa for 7.2 nm nanocrystals to 37 GPa for 3.6 nm nanocrystals. All nanocrystals were found to remain in the α structure even after release of pressure. The transition pressure was also found, for a constant size (5.7 nm) to be strongly dependent on the degree of aggregation of the nanocrystals, increasing from 30 GPa for completely dissolved nanocrystals to 45 GPa for strongly aggregated nanocrystals. Furthermore, the x-ray diffraction pattern of the pressure induced α phase demonstrated a decrease in intensity for certain select peaks. Together, these observations were used to make a complete picture of the phase transition in nanocrystalline systems. The size dependence of the transition was interpreted as resulting from the extremely high surface energy of the α phase which would increase the thermodynamic offset and thereby increase the kinetic barrier to transition that must be overridden with pressure

  10. Neutron powder diffraction of small-volume samples at high pressure using compact opposed-anvil cells and focused beam

    International Nuclear Information System (INIS)

    Okuchi, T; Sasaki, S; Ohno, Y; Abe, J; Osakabe, T; Hattori, T; Sano-Furukawa, A; Utsumi, W; Arima, H; Harjo, S; Ito, T; Aizawa, K; Komatsu, K; Kagi, H

    2012-01-01

    Neutron powder diffraction techniques of small-volume samples at high pressure using compact opposed-anvil cells were developed at J-PARC pulsed neutron source. For this purpose we apply a few types of super-hard materials as opposed anvils with culet diameters between 3 to 5 mm. Generated pressures with these anvils were up to 9 GPa for 2 to 4 mm 3 and up to 14 GPa for 0.7 mm 3 sample volumes, which not only depends on the anvil geometry and material but even more depends on the metallic gasket geometry and material. A representative anvil geometry with 4 mm in culet diameter, along with TiZr 'null alloy' metallic gasket containing varying sample volumes, were then applied to time-of-flight neutron powder diffraction experiments, where methane hydrate of 4 mm 3 volume and lead of 0.7 mm 3 volume were separately measured and their signal-to-background ratios were evaluated. A neutron-focusing optics was used to concentrate the neutron beam into these small-volume samples to increase the intensity of diffraction. Although spurious diffraction peaks from the anvils were prominent, more than seven diffraction peaks are clearly observed from both of the samples. In spite of the smaller sample capacity than previous standard high-pressure apparatus for neutron, it is concluded that the opposed-anvil cells will become alternative apparatuses for neutron scattering at strong pulsed neutron sources where sufficient neutron intensity was granted.

  11. Single-crystal X-ray and neutron powder diffraction investigation of the phase transition in tetrachlorobenzene.

    Science.gov (United States)

    Barnett, Sarah A; Broder, Charlotte K; Shankland, Kenneth; David, William I F; Ibberson, Richard M; Tocher, Derek A

    2006-04-01

    The polymorphic phase transition of 1,2,4,5-tetrachlorobenzene (TCB) has been investigated using neutron powder diffraction and single-crystal X-ray diffraction. The diffraction experiments show a reversible phase change that occurs as a function of temperature with no apparent loss of sample quality on transition between the two phases. Neutron powder diffraction gives detailed information on the molecular structural changes and lattice parameters from 2 K to room temperature. The structure of the low-temperature form has been elucidated for the first time using single-crystal X-ray diffraction. Comparison of the alpha and beta structures show that they are both based on the same sheet motif, with the differences between the two being very subtle, except in terms of crystal symmetry. Detailed analysis of the structures revealed the changes required for inter-conversion. A computational polymorph search showed that these two sheet structures are more thermodynamically stable than alternative herringbone-type structures.

  12. Small-angle x-ray scattering/diffraction system for studies of biological and other materials at the Stanford Synchrotron Radiation Laboratory (abstract)

    International Nuclear Information System (INIS)

    Wakatsuki, S.; Hodgson, K.O.; Eliezer, D.; Rice, M.; Hubbard, S.; Gillis, N.; Doniach, S.; Spann, U.

    1992-01-01

    A versatile small-angle x-ray diffraction/scattering system has been developed at Stanford Synchrotron Radiation Laboratory for studies of biological and other materials. The system includes two sets of collimation slits separated by an ionization chamber, a sample holder cooled by a circulation bath, a vacuum/He scattering path after the sample holder and a detector, either a linear one-dimensional position-sensitive proportional counter or a position-sensitive quadrant detector. Data aquisition is controlled by a VAXstation through a CAMAC interface. Menu-driven data acquisition and on-line analysis software has been developed. The system can be used to collect small- to intermediate-angle x-ray scattering and diffraction data. Monochromatic, anomalous, and time-resolved diffraction/scattering experiments are possible. A time-resolved spectrophotometer using photodiode arrays has also been developed for simultaneous measurements of optical absorption spectra and x-ray scattering/diffraction

  13. Study of polymorphism of Atenolol and Captopril antihypertensives using x-ray powder diffraction and Rietveld refinement

    Science.gov (United States)

    Sato, Juliana; Ferreira, Fabio

    2013-03-01

    Characterization of bulk drugs has become increasingly important in the pharmaceutical industry. X-ray powder diffractometry is an effective technique for the identification of crystalline solid-phase drugs. The technique is unique, since it combines specificity with a high degree of accuracy for the characterization of pharmaceuticals in solid state and is an especially useful method to describe the possible polymorphic behavior of drugs substances. In this work X-ray diffraction data have been obtained for two well-known antihypertensive drugs currently being administered in tablet form. They include atenolol and captopril. Atenolol and captopril were purchased from drugstore. The characterizations of the atenolol and captopril samples were carried out by FTIR spectroscopy and X-ray powder diffraction (XRPD). We would like to thank the Brazilian agencies CNPq and FAPESP for their financial support.

  14. The crystal structures and powder diffraction patterns of the uranium tellurides

    Energy Technology Data Exchange (ETDEWEB)

    Snyder, R.L. (State Univ. of New York, Alfred, NY (USA). Inst. of Ceramic Superconductivity); Nichols, M.C.; Boehme, D.R. (Sandia National Labs., Livermore, CA (USA))

    1990-10-03

    A critical review of all of the reported structures and powder diffraction patterns in the uranium telluride system has been undertaken. Structures that are correct: Cubic -- UTe: no experimental pattern exists. Retain calculated 15--865. Cubic --U{sub 3}Te{sub 4}: retain the poor quality 12--610 but adopt the pattern calculated here. Cubic U{sub 2}Te{sub 3}: no experimental pattern exists. Adopt pattern calculated here. Orthorhombic UTe{sub 2}: Adopt the new pattern of Boehme et al. Monoclinic {alpha}UTe{sub 3} Adopt the new pattern of Boehme et al. Monoclinic {alpha}UTe{sub 3} Adopt the new pattern of Boehme et al. Orthorhombic {beta}UTe{sub 3}: Adopt pattern calculated here. Orthorhombic UTe{sub 5}: Adopt the new pattern of Boehme et al. Structures in need of refinement: Orthorhombic U{sub 2}Te{sub 3}:Adopt pattern calculated here over 34--807. Hexagonal U{sub 7}Te{sub 12}: Adopt pattern calculated here but retain 24--1368. Orthorhombic UTe{sub 1.78}: Adopt pattern calculated here and retain our modified 21--1404 reported for U{sub 4}Te{sub 7}. Orthorhombic UTe{sub 2.5}: Adopt pattern calculated here. Orthorhombic UTe{sub 3.4}: Accept recent pattern of Boehme et al. Phases for which no structures or reliable patterns exist: Orthorhombic U{sub 3}Te{sub 4}: no published pattern. Tetragonal U{sub 3}Te{sub 5}: three patterns 21--1407, 34--766 and 34--896 exit but all are of very poor quality. Phases which probably do not exist: Tetragonal UTe{sub 1.78}, Tetragonal UTe{sub 2}, Cubic UTe{sub 2} U{sub 3}Te{sub 7}(21--1402), U{sub 3}Te{sub 8}(21--1406).

  15. High-temperature structural phase transitions in neighborite: a high-resolution neutron powder diffraction investigation

    Science.gov (United States)

    Knight, Kevin S.; Price, G. David; Stuart, John A.; Wood, Ian G.

    2015-01-01

    The nature of the apparently continuous structural phase transition at 1,049 K in the perovskite-structured, MgSiO3 isomorph, neighborite (NaMgF3), from the orthorhombic ( Pbnm) hettotype phase to the cubic () aristotype structure, has been re-investigated using high-resolution, time-of-flight neutron powder diffraction. Using data collected at 1 K intervals close to the nominal phase transition temperature, the temperature dependence of the intensities of superlattice reflections at the M point and the R point of the pseudocubic Brillouin zone indicate the existence of a new intermediate tetragonal phase in space group P4/ mbm, with a narrow phase field extending from ~1,046.5 to ~1,048.5 K, at ambient pressure. Group theoretical analysis shows that the structural transitions identified in this study, Pbnm- P4/ mbm, and P4/ mbm-, are permitted to be second order. The observation of the tetragonal phase resolves the longstanding issue of why the high-temperature phase transition, previously identified as Pbnm-, and which would be expected to be first order under Landau theory, is in fact found to be continuous. Analysis of the pseudocubic shear strain shows it to vary with a critical exponent of 0.5 implying that the phase transition from Pbnm to P4/ mbm is tricritical in character. The large librational modes that exist in the MgF6 octahedron at high temperature, and the use of Gaussian probability density functions to describe atomic displacements, result in apparent bond shortening in the Mg-F distances, making mode amplitude determination an unreliable method for determination of the critical exponent from internal coordinates. Crystal structures are reported for the three phases of NaMgF3 at 1,033 K ( Pbnm), 1,047 K ( P4/ mbm) and 1,049 K ().

  16. Application of combined multivariate techniques for the description of time-resolved powder X-ray diffraction data

    Czech Academy of Sciences Publication Activity Database

    Taris, A.; Grosso, M.; Brundu, M.; Guida, V.; Viani, Alberto

    2017-01-01

    Roč. 50, č. 2 (2017), s. 451-461 ISSN 1600-5767 R&D Projects: GA MŠk(CZ) LO1219 Keywords : in situ X-ray powder diffraction * amorphous content * chemically bonded ceramics * statistical total correlation spectroscopy * multivariate curve resolution Subject RIV: JJ - Other Materials OBOR OECD: Materials engineering Impact factor: 2.495, year: 2016 http://journals.iucr.org/j/issues/2017/02/00/ap5006/index.html

  17. Iron compounds in brazilian pre-columbian pigments identified by 57Fe Moessbauer spectroscopy and X-ray powder diffraction

    International Nuclear Information System (INIS)

    Araujo, F.F.T. de; Araujo, M.A.B. de; Vieira, V.W.; Frankel, R.B.

    1988-01-01

    Moessbauer spectroscopy and X-ray powder diffraction have been used to identify iron compounds in pre-Columbian pigments, probably used for art decorating, collected from the oldest archaeological site of Early Man presently known in America at Sao Raimundo Nonato, in Northeastern Brazil. The iron compounds were idenfied as being alpha-Fe203 (haematite) with full Morin transition supressed and small particles of alpha-FeOOH (goethite). (author)

  18. The role of iron in tetrahedrite and tennantite determined by Rietveld refinement of neutron powder diffraction data

    DEFF Research Database (Denmark)

    Andreasen, Jens Wenzel; Makovicky, Emil; Lebech, Bente

    2008-01-01

    Rietveld refinement of neutron powder diffraction data on four samples of synthetic, iron-bearing tetrahedrite (Cu12-xFexSb4S13) with x = 0.28, 0.69, 0.91, 2.19 and four samples of synthetic tennantite (Cu12-xFexAs4S13) with x = 0.33, 0.38, 0.86, 1.5 indicate unambiguously that iron is incorporated...

  19. Germanate with three-dimensional 12 × 12 × 11-ring channels solved by X-ray powder diffraction with charge-flipping algorithm.

    Science.gov (United States)

    Xu, Yan; Liu, Leifeng; Chevrier, Daniel M; Sun, Junliang; Zhang, Peng; Yu, Jihong

    2013-09-16

    A new open-framework germanate, denoted as GeO-JU90, was prepared by the hydrothermal synthesis method using 1,5-bis(methylpyrrolidinium)pentane dihydroxide as the organic structure-directing agent (SDA). The structure of GeO-JU90 was determined from synchrotron X-ray powder diffraction (XRPD) data using the charge-flipping algorithm. It revealed a complicated framework structure containing 11 Ge atoms in the asymmetric unit. The framework is built of 7-connected Ge7 clusters and additional tetrahedral GeO3(OH) units forming a new three-dimensional interrupted framework with interesting 12 × 12 × 11-ring intersecting channels. The Ge K-edge extended X-ray absorption fine structure (EXAFS) analysis was performed to provide the local structural information around Ge atoms, giving rise to a first-shell contribution from about 4.2(2) O atoms at the average distance of 1.750(8) Å. The guest species in the channels were subsequently determined by the simulated annealing method from XRPD data combining with other characterization techniques, e.g., (13)C NMR spectroscopy, infrared spectroscopy (FTIR), compositional analyses, and thermogravimetric analysis (TGA). Crystallographic data |(C15N2H32)(NH4)|[Ge11O21.5(OH)4], orthorhombic Ama2 (No. 40), a = 37.82959 Å, b = 15.24373 Å, c = 12.83659 Å, and Z = 8.

  20. A Rietveld refinement method for angular- and wavelength-dispersive neutron time-of-flight powder diffraction data.

    Science.gov (United States)

    Jacobs, Philipp; Houben, Andreas; Schweika, Werner; Tchougréeff, Andrei L; Dronskowski, Richard

    2015-12-01

    This paper introduces a two-dimensional extension of the well established Rietveld refinement method for modeling neutron time-of-flight powder diffraction data. The novel approach takes into account the variation of two parameters, diffraction angle 2θ and wavelength λ, to optimally adapt to the varying resolution function in diffraction experiments. By doing so, the refinement against angular- and wavelength-dispersive data gets rid of common data-reduction steps and also avoids the loss of high-resolution information typically introduced by integration. In a case study using a numerically simulated diffraction pattern of Rh 0.81 Fe 3.19 N taking into account the layout of the future POWTEX instrument, the profile function as parameterized in 2θ and λ is extracted. As a proof-of-concept, the resulting instrument parameterization is then utilized to perform a typical refinement of the angular- and wavelength-dispersive diffraction pattern of CuNCN, yielding excellent residuals within feasible computational efforts. Another proof-of-concept is carried out by applying the same approach to a real neutron diffraction data set of CuNCN obtained from the POWGEN instrument at the Spallation Neutron Source in Oak Ridge. The paper highlights the general importance of the novel approach for data analysis at neutron time-of-flight diffractometers and its possible inclusion within existing Rietveld software packages.

  1. Clay pigment structure characterisation as a guide for provenance determination-a comparison between laboratory powder micro-XRD and synchrotron radiation XRD

    Czech Academy of Sciences Publication Activity Database

    Švarcová, Silvie; Bezdička, Petr; Hradil, David; Hradilová, J.; Žižak, I.

    2011-01-01

    Roč. 399, č. 1 (2011), s. 331-336 ISSN 1618-2642 Institutional research plan: CEZ:AV0Z40320502 Keywords : powder X-ray micro-diffraction * kaolinite * pigment provenance Subject RIV: CA - Inorganic Chemistry Impact factor: 3.778, year: 2011

  2. Synchrotron light

    International Nuclear Information System (INIS)

    2001-01-01

    'Synchrotron Light' is an interactive and detailed introduction to the physics and technology of the generation of coherent radiation from accelerators as well as to its widespread high-tech applications in science, medicine and engineering. The topics covered are the interaction of light and matter, the technology of synchrotron light sources, spectroscopy, imaging, scattering and diffraction of X-rays, and applications to materials science, biology, biochemistry, medicine, chemistry, food and pharmaceutical technology. All synchrotron light facilities are introduced with their home-page addresses. 'Synchrotron Light' provides an instructive and comprehensive multimedia learning tool for students, experienced practitioners and novices wishing to apply synchrotron radiation in their future work. Its multiple-entry points permit an easy exploration of the CD-Rom according to the users knowledge and interest. 2-D and 3-D animations and virtual reconstruction with computer-generated images guide visitors into the scientific and technical world of a synchrotron and into the applications of synchrotron radiation. This bilingual (English and French) CD-Rom can be used for self-teaching and in courses at various levels in physics, chemistry, engineering, and biology. (author)

  3. Absolute determination by X-ray diffraction of a binary or ternary mixture: nickel oxide and fluoride in a nickel powder (1960)

    International Nuclear Information System (INIS)

    Charpin, P.; Hauptman, A.

    1960-01-01

    The method employed is based upon the comparison between computed and measured intensities for conveniently selected X-Ray diffraction lines of each component of the powder. Care must be taken to allow for absorption, both inside each grain and in overall sample. This method has been applied to the determination of nickel oxide and fluoride in a nickel powder. (author) [fr

  4. submitter Digital Image Correlation of 2D X-ray Powder Diffraction Data for Lattice Strain Evaluation

    CERN Document Server

    Zhang, Hongjia; Salvati, Enrico; Daisenberger, Dominik; Lunt, Alexander J G; Fong, Kai Soon; Song, Xu; Korsunsky, Alexander M

    2018-01-01

    High energy 2D X-ray powder diffraction experiments are widely used for lattice strain measurement. The 2D to 1D conversion of diffraction patterns is a necessary step used to prepare the data for full pattern refinement, but is inefficient when only peak centre position information is required for lattice strain evaluation. The multi-step conversion process is likely to lead to increased errors associated with the ‘caking’ (radial binning) or fitting procedures. A new method is proposed here that relies on direct Digital Image Correlation analysis of 2D X-ray powder diffraction patterns (XRD-DIC, for short). As an example of using XRD-DIC, residual strain values along the central line in a Mg AZ31B alloy bar after 3-point bending are calculated by using both XRD-DIC and the conventional ‘caking’ with fitting procedures. Comparison of the results for strain values in different azimuthal angles demonstrates excellent agreement between the two methods. The principal strains and directions are calculated...

  5. Clinopyroxenes still trapped in diamonds: high-energy synchrotron X-ray diffraction as a chemical probe

    Science.gov (United States)

    Casati, Nicola; Nestola, Fabrizio; Alvaro, Matteo; Wilhelm, Heribert; Kleppe, Annette; Nimis, Paolo; Harris, Jeffrey W.

    2014-05-01

    Clinopyroxenes are mainly Ca-Na-Fe-Mg-silicates constituting a significant portion of the Earth's upper mantle up to 20% of such shell of our planet. They could be found as typical mineral inclusions in diamonds being diopsidic and omphacitic in composition and, together with garnets, cover a key role in providing indications concerning the source rock in which the diamond crystallize. In detail, it is well known that eclogitic diamonds are characterized by clinopyroxenes with omphacitic compositions (about Ca0.5Na0.5Mg0.5Al0.5Si2O6) whereas peridotitic diamonds show clinopyroxenes very rich in the diopside end-member (CaMgSi2O6). In order to get direct chemical composition on the inclusions, and therefore on the diamond origin source, it is obviously necessary to extract them breaking and/or polishing the diamond host. However, a non-destructive investigation of an inclusion still trapped in a diamond is useful and important for different reasons: (1) the inclusions could be under pressure and their crystal structure can be modified if the pressure is released by the extraction; (2) the residual pressure on the inclusion can provide information about the formation pressure of the diamond (e.g. Nestola et al. 2011 and references therein); (3) the morphology and growth relationships of the inclusion with the host diamond can provide indications about its protogenetic vs. syngenetic and/or epigenetic nature; and (4) preservation of the diamond surface growth features can maintain crucial information on late oxidation processes (Fedortchouk et al. 2011). However the available methods to measure the composition of the inclusions implies to destroy the sample. The aim of this work is to obtain chemical information on the inclusions still trapped in their diamond host and therefore to indicate the diamond origin without extracting the inclusions. The work was carried out by single crystal X-ray diffraction using a new experimental approach by high energy synchrotron

  6. A comparison between different X-ray diffraction line broadening analysis methods for nanocrystalline ball-milled FCC powders

    Energy Technology Data Exchange (ETDEWEB)

    Soleimanian, V. [Shahrekord University, Department of Physics, Faculty of Sciences, P.O. Box 115, Shahrekord (Iran, Islamic Republic of); Shahrekord University, Nanotechnology Research Center, Shahrekord (Iran, Islamic Republic of); Mojtahedi, M. [Pooya Gharb Branch of University of Applied Science and Technology, Department of Materials Engineering, Kermanshah (Iran, Islamic Republic of)

    2015-06-15

    The microstructural characteristics of aluminum, copper and nickel powders are investigated using different X-ray diffraction line broadening analysis approaches. Prior to analysis, the powders were ball-milled to produce a nanocrystalline structure with high density of probable types of lattice defects. A variety of methods, including Scherrer, Williamson-Smallman, Williamson-Hall, Warren-Averbach, modified Williamson-Hall, modified Warren-Averbach, Rietveld refinement and whole powder pattern modeling (WPPM) approaches are applied. In this way, microstructural characteristics such as crystallite size, microstrain, dislocation density, effective outer cut-off radius of dislocations and the probability of twining and stacking faults are calculated. On the other hand, the results of conventional and advanced line broadening analysis methods are compared. It is revealed that the density of linear and planar defects in the mechanically deformed aluminum powder is significantly smaller than that of copper and nickel, as well as the level of anisotropic strain broadening. Moreover, the WPPM procedure provided a better profile fitting with more accurate results. (orig.)

  7. Analysis of an industrial production suspension of Bacillus lentus subtilisin crystals by powder diffraction: a powerful quality-control tool

    DEFF Research Database (Denmark)

    Frankær, Christian Grundahl; Moroz, Olga V.; Turkenburg, Johan P.

    2014-01-01

    in the production suspension, albeit with the 1ndq -like microcrystals predominating. It is shown how the two techniques can provide invaluable and complementary information for such a production suspension and it is proposed that XRPD provides an excellent quality-control tool for such suspensions....... production suspension corresponded to space group P212121, with unit-cell parameters a = 47.65, b = 62.43, c = 75.74 Å, equivalent to those for a known orthorhombic crystal form (PDB entry 1ndq ). MX using synchrotron beamlines at the Diamond Light Source with beam dimensions of 20 × 20 µm was subsequently...... used to study the largest crystals present in the suspension, with diffraction data being collected from two single crystals (~20 × 20 × 60 µm) to resolutions of 1.40 and 1.57 Å, respectively. Both structures also belonged to space group P212121, but were quite distinct from the dominant form...

  8. A program for the derivation of crystal unit cell parameters from X-ray powder diffraction measurements

    International Nuclear Information System (INIS)

    Ferguson, I.F.; Rogerson, A.H.

    1984-01-01

    The program, FIRESTAR, determines the dimensions of a crystallographic unit cell from a set of X-ray powder diffraction measurements corresponding to a set of Bragg reflections, provided that the crystal system applicable is known and the Bragg reflections have been indexed. The program includes a range of possible extrapolation functions, and the data may be weighted. Provision is made for detecting and rejecting a single 'bad' measurement, and then rejecting measurements which lie outside an error limit set in the input data. (orig.)

  9. A comparison of time-of-flight and Larmor modulation neutron powder diffraction at a continuous reactor source

    CERN Document Server

    Mulder, F M

    1999-01-01

    A neutron powder diffraction instrument for application at a continuous reactor source based on time-of-flight (TOF) is compared with an instrument based on Larmor modulation (LM). For instruments with a similar wave-vector resolution (delta q/q=4x10 sup - sup 3) it is found that the signal-to-noise ratios in a TOF experiment are generally better when using a wide wavelength neutron spectrum. This is caused by the fact that the noise in a LM experiment comes from the integrated neutron flux scattered in the detector, while in TOF the noise stems only from the intensity scattered into individual time channels.

  10. High-pressure and high-temperature powder diffraction on molybdenum diphosphide, MoP{sub 2}

    Energy Technology Data Exchange (ETDEWEB)

    Soto, V. [Centro de Investigacion Cientifica y de Educacion Superior de Ensenada, Esenada (Mexico); Knorr, K.; Ehm, L. [Christian-Albrechts-Univ. zu Kiel, Inst. fuer Geowissenschaften, Mineralogie/Kristallographie, Kiel (Germany); Baehtz, C. [HASYLAB Hamburg and TU Darmstadt, Materialwissenschaften, Darmstadt (Germany); Winkler, B. [Johann-Wolfgang-Goethe Univ. Frankfurt-Main, Mineralogie, Frankfurt/M. (Germany); Avalos-Borja, M. [Centro de Ciencias de la Materia Condensada, Univ. Nacional Autonoma de Mexico, Ensenada, BC (Mexico)

    2004-07-01

    The isothermal compressibility and bulk thermal expansion of molybdenum diphosphide, MoP{sub 2}, were measured by in-situ X-ray powder diffraction from ambient conditions to 6.8 GPa and 839 K, respectively. A small anisotropy of the compressibilities in MoP{sub 2} appears to be governed by non-bonding interactions in this layer-like material. The thermal expansion data are compared to molybdenum phosphide, MoP, which was measured to 1262 K. (orig.)

  11. Applications of one-dimensional position-sensitive detectors for neutron diffraction experiments on powders and liquids

    International Nuclear Information System (INIS)

    Riekel, C.

    1983-01-01

    The applications of one-dimensional position sensitive detectors (PSDs) are reviewed. The detectors used are multiwire detectors based on the principle of gas-filled proportional counters. The uses include the neutron diffraction from powders and liquids in the study of chemical reactions and phase transitions. However, the angular range and wire separation are insufficient for many experiments. In particular the data acquisition and processing are inadequate for real time experiments with tsub(s) values of seconds or less. (tsub(s) - measuring time per spectrum). From the results obtained it should be possible to optimize the construction of a new 160 0 PSD. (U.K.)

  12. Powder neutron and X-ray diffraction study of La4CO3O10.00

    International Nuclear Information System (INIS)

    Hansteen, O.H.; Fjellvag, H.; Hauback, B.C.

    1998-01-01

    The crystal structure of stoichiometric La 4 CO 3 O 10.00 is of the Ruddlesden-Popper type and contains slabs of triple perovskite layers separated by rock salt layers, the composition corresponding to n = 3 in the A n+1 B n O 3n+1 series. On heating, the slightly orthorhombically deformed structure converts into a tetragonal one at around 840 K. Antiferromagnetic ordering occurs below T N ≅ 10 K. Crystal structure data from powder neutron diffraction are presented. Slight line broadening of some X-ray reflections and a few, weak additional neutron reflections indicates that the true symmetry is lower than Fmmm. (authors)

  13. Rietveld refinement of In{sub 2}S{sub 3} using neutron and X-ray powder diffraction data

    Energy Technology Data Exchange (ETDEWEB)

    Rampersadh, Niyum S.; Venter, Andrew M.; Billing, David G

    2004-07-15

    Powder neutron and X-ray diffraction data for indium sulfide are reported. The lattice parameters obtained from a Rietveld refinement for the neutron data are: a=7.5937 (6) A; c=32.352 (3) A; V=1865.6 (3) A{sup 3} and for X-ray data are: a=7.6172 (1) A; c=32.3307 (8) A; V=1875.86 (6) A{sup 3}. The crystal system was taken to be tetragonal (space group I4{sub 1}/amd)

  14. In situ powder neutron diffraction study of non-stoichiometric phase formation during the hydrogenation of Li3N.

    Science.gov (United States)

    Bull, Daniel J; Sorbie, Natalie; Baldissin, Gael; Moser, David; Telling, Mark T F; Smith, Ronald I; Gregory, Duncan H; Ross, D Keith

    2011-01-01

    The hydrogenation of Li3N at low chemical potential has been studied in situ by time-of-flight powder neutron diffraction and the formation of a non-stoichiometric Li4-2xNH phase and Li4NH observed. The results are interpreted in terms of a model for the reaction pathway involving the production of Li4NH and Li2NH, which subsequently react together to form Li4-2xNH. Possible mechanisms for the production of Li4NH from the hydrogenation of Li3N are discussed.

  15. X-ray powder diffraction and EXAFS studies on SnAPO-5 and Cu : SnAPO-5

    DEFF Research Database (Denmark)

    Flavell, W. R.; Nicholson, D. G.; Nilsen, M. H.

    2001-01-01

    to the tetrahedral faces. Based on crystal chemical considerations it is suggested that tin is five-coordinate in a trigonal bipyramid with its second axial corner protruding into the extra-framework area. For the copper-incorporated material, Cu : SnAPO-5, EXAFS shows that the copper environment is tetragonally...... distorted octahedral. Powder diffraction confirms an extra-framework disordered square-planar copper-coordination connected to two framework oxygens by longer axial bonds. EXAFS results of calcined Cu : SnAPO-5 show that copper is sited near the tin sites in the framework....

  16. Identification of copper-based green pigments in Jaume Huguet's Gothic altarpieces by Fourier transform infrared microspectroscopy and synchrotron radiation X-ray diffraction.

    Science.gov (United States)

    Salvadó, N; Pradell, T; Pantos, E; Papiz, M Z; Molera, J; Seco, M; Vendrell-Saz, M

    2002-07-01

    The scientific investigation of ancient paintings gives a unique insight into ancient painting techniques and their evolution through time and geographic location. This study deals with the identification of the green pigments used by one of the most important Catalan masters in Gothic times, Jaume Huguet. Other pigments and materials have also been characterized by means of conventional techniques such as optical microscopy, scanning electron microscopy and Fourier transform infrared spectroscopy. Synchrotron radiation X-ray diffraction has been used to produce maps of phases at a spatial resolution of 100 microm across chromatic layers.

  17. In situ synchrotron X-ray diffraction study of deformation behavior and load transfer in a Ti2Ni-NiTi composite

    Science.gov (United States)

    Zhang, Junsong; Liu, Yinong; Ren, Yang; Huan, Yong; Hao, Shijie; Yu, Cun; Shao, Yang; Ru, Yadong; Jiang, Daqiang; Cui, Lishan

    2014-07-01

    The deformation behavior and load transfer of a dual-phase composite composed of martensite NiTi embedded in brittle Ti2Ni matrices were investigated by using in situ synchrotron x-ray diffraction during compression. The composite exhibits a stage-wise deformation feature and a double-yielding phenomenon, which were caused by the interaction between Ti2Ni and NiTi with alternative microscopic deformation mechanism. No load transfer occurs from the soft NiTi dendrites to the hard Ti2Ni matrices during the pseudoplastic deformation (detwinning) of NiTi, which is significantly different from that previously reported in bulk metallic glasses matrices composites.

  18. Residual stresses and structural integrity in nuclear structural materials: recent developments and results from neutron and synchrotron x-ray diffraction experiments

    International Nuclear Information System (INIS)

    Steuwer, A.; Daniels, JE

    2008-01-01

    Over the last few years, significant progress has been made in the investigation of residual stresses over a variety of length scales in nuclear structural materials, ranging from stainless steels to hydrided zirconium alloys. In this manuscript we review some of these developments, such as, in-situ characterization of stresses at crack tips in steels and zirconium alloys, residual stresses around welds, and the characterization of hydrided zirconium alloys. Neutron and synchrotron X-ray diffraction are essential and complementary tools in this approach, and their applicability to structural integrity issues is discussed in view of existing and future large-scale research facilities. (au)

  19. Synchrotron-Based High Angle Resolution and High Lateral Resolution X-ray Diffraction: Revealing Lead White Pigment Qualities in Old Masters Paintings.

    Science.gov (United States)

    Gonzalez, V; Wallez, G; Calligaro, T; Cotte, M; De Nolf, W; Eveno, M; Ravaud, E; Menu, M

    2017-12-19

    Microsamples collected on 27 major paintings by Old European Masters dating from the 14th to the late 19th centuries were analyzed using synchrotron-based X-ray diffraction. Two complementary analytical configurations were used at beamlines ID22 (high angle resolution) and ID21 (high lateral resolution), in order to highlight markers of the different grades of the lead white pigments (mixture of cerussite PbCO 3 and hydrocerussite Pb 3 (CO 3 ) 2 (OH) 2 ). Rietveld analysis and crystalline phases mapping at the microscale revealed the composition and microstructure of the pigments, shedding light on the preparation recipes and pigment choices of the artists through History.

  20. Advances in martensitic transformations in Cu-based shape memory alloys achieved by in situ neutron and synchrotron X-ray diffraction methods

    Czech Academy of Sciences Publication Activity Database

    Malard, B.; Šittner, Petr; Berveiller, S.; Patoor, E.

    2012-01-01

    Roč. 13, č. 3 (2012), s. 280-292 ISSN 1631-0705 R&D Projects: GA ČR GAP108/10/1296; GA ČR GAP107/12/0800 EU Projects: European Commission(XE) 262806 - SmartNets Institutional research plan: CEZ:AV0Z10100520 Keywords : stress induced martensitic transformation * Cu-based shape memory alloys * neutron diffraction * X-ray * synchrotron * in situ * multiscale analysis Subject RIV: BM - Solid Matter Physics ; Magnetism Impact factor: 1.818, year: 2012

  1. Experimental issues in in-situ synchrotron x-ray diffraction at high pressure and temperature by using a laser-heated diamond-anvil cell

    International Nuclear Information System (INIS)

    Yoo, C.S.

    1997-01-01

    An integrated technique of diamond-anvil cell, laser-heating and synchrotron x-ray diffraction technologies is capable of structural investigation of condensed matter in an extended region of high pressures and temperatures above 100 GPa and 3000 K. The feasibility of this technique to obtain reliable data, however, strongly depends on several experimental issues, including optical and x-ray setups, thermal gradients, pressure homogeneity, preferred orientation, and chemical reaction. In this paper, we discuss about these experimental issues together with future perspectives of this technique for obtaining accurate data

  2. Neutron powder diffraction study on Mg sup 1 sup 1 B sub 2 synthesized by different procedures

    CERN Document Server

    Oikawa, K; Arai, M; Mochiku, T; Takeya, H; Furuyama, M; Kamisawa, S; Kadowaki, K

    2002-01-01

    The crystal structure of a new superconducting material, MgB sub 2 , was studied by high-resolution neutron powder diffraction as a function of temperature from 8K to 305K. Two samples of Mg sup 1 sup 1 B sub 2 were measured; one was synthesized for 2d at 1050degC, and the other one was done for 1d at 1100degC. All of the diffraction data were precisely refined by the Rietveld method, and we confirmed that there was no clear anomaly on the temperature dependence of the lattice constants around T sub c for both samples. The difference in sample synthesis procedures affects the profile shapes of the 001 reflections, whereas the hh0 lines are almost the same.

  3. Powder Handling Device for X-ray Diffraction Analysis with Minimal Sample Preparation, Phase I

    Data.gov (United States)

    National Aeronautics and Space Administration — This project consists of developing a Vibrating Sample Holder (VSH) for planetary X-Ray Diffraction (XRD) instruments. The principle of this novel sample handling...

  4. Synchrotron radiation microbeam X-ray diffraction for nondestructive assessments of local structural properties of faceted InGaN/GaN quantum wells

    Science.gov (United States)

    Sakaki, Atsushi; Funato, Mitsuru; Kawamura, Tomoaki; Araki, Jun; Kawakami, Yoichi

    2018-03-01

    Synchrotron radiation (SR) X-ray diffraction with a sub-µm spatial resolution is used to nondestructively evaluate the local thickness and alloy composition of three-dimensionally faceted InGaN/GaN quantum wells (QWs). The (0001) facet QW on a trapezoidal structure composed of (0001), \\{ 11\\bar{2}2\\} , and \\{ 11\\bar{2}0\\} facets is nonuniform, most likely owing to the migration of adatoms between facets. The thickness and composition markedly vary within a short distance for the \\{ 11\\bar{2}2\\} facet QW of another pyramidal structure. The QW parameters acquired by SR microbeam X-ray diffraction reproduce the local emission property assessed by cathodoluminescence, thereby indicating the high reliability of this method.

  5. Monitoring of the YBa2Cu3O7 synthesis by X-ray powder diffraction

    International Nuclear Information System (INIS)

    Gonzalez G, J.C.; Osorio A, Ana M.; Bejar R, Manuel; Bustamante D, Angel

    2011-01-01

    We study the formation dynamics of the YBa 2 Cu 3 O 7 superconducting phase, from Y, Ba and Cu acetates prepared by the Sol-Gel method. The monitoring is done through by Rietveld refinement of the X-ray powder diffractograms at the end product resulting in three specific stages of the thermal treatment: (a) precursor, (b) calcined and (c) sinterized. (author).

  6. An attempt of in vivo X-ray diffraction analysis of kidney stones with the use of synchrotron radiation

    Energy Technology Data Exchange (ETDEWEB)

    Ancharov, A.I. [Institute of Solid State Chemistry and Mechanochemistry SB RAS, Kutateladze str.18, Novosibirsk 630218 (Russian Federation)]. E-mail: ancharov@mail.ru; Nizovskii, A.I. [Boreskov institute of catalysis SB RAS, Novosibirsk (Russian Federation); Gridnev, S.A. [Central city hospital, Berdsk (Russian Federation); Feofilov, I.V. [State regional clinical hospital, Novosibirsk (Russian Federation); Vichkanov, A.N. [State regional clinical hospital, Omsk (Russian Federation)

    2005-05-01

    Estimation of opportunities of the direct analysis of phase structure kidney stones directly in an organism of the patient with the use of synchrotron radiations (SR). Carrying out of experiments on special modelled object 'phantom'. Estimation of the radiation dose.

  7. Characterisation of the UFXC32k hybrid pixel detector for time-resolved pump-probe diffraction experiments at Synchrotron SOLEIL

    Science.gov (United States)

    Dawiec, A.; Maj, P.; Ciavardini, A.; Gryboś, P.; Laulhé, C.; Menneglier, C.; Szczygieł, R.

    2017-03-01

    The experimental set-up for time-resolved studies of ultra-fast photo-induced structural dynamics at the Synchrotron SOLEIL is based on a general pump-probe scheme that has been developed and implemented on the CRISTAL hard X-ray diffraction beamline [1,2]. In a so-called pump-probe cycle, the sample is excited with an ultra-short laser pulse of ≈40 fs duration (the pump), and induced changes in its atomic structure are studied by measuring, with a precisely controlled delay, a diffraction pattern from a single pulse of synchrotron radiation (the probe) with a 2-D pixel detector. An improvement to the classical scheme is proposed, where the sample's response is probed at two different delays after each laser excitation. The first measurement at short delays allows studying the photo-induced dynamics. The second one is a reference measurement taken after sample's relaxation, which permits detection of drifts in the experimental conditions (e.g. beam misalignment, sample degradation). A hybrid pixel detector with a very fast readout time, a high dynamic range and extended linearity was tested to achieve the experiment objectives. In this paper, the first results obtained with the UFXC32k single photon counting detector are presented.

  8. A 2D MWPC area detector for use with synchrotron X-radiation at the Daresbury Laboratory for small angle diffraction and scattering

    International Nuclear Information System (INIS)

    Helliwell, J.R.; Hughes, G.; Przybylski, M.M.; Ridley, P.A.; Sumner, I.; Bateman, J.E.; Connolly, J.F.; Stephenson, R.

    1982-01-01

    A 2D multiwire proportional chamber area detector is being developed to provide a real time data acquisition system for small angle scattering and diffraction experiments with synchrotron X-radiation at the Daresbury synchrotron radiation source (SRS). The chamber has a circular aperture, 200 mm diameter with an anode and cathode wire pitch of 1 mm; a front cathode-anode spacing of 6 mm and a 6 mm spacing between anode and rear cathode. A 1 mm thick front beryllium window and a rear aluminium cover plate with indium seals provide a gas-tight system. Previous experiments with a similar chamber design allowed continual use of the chamber for up to 2 years without refill. A digitising time of 2 μs is expected based on a 260 mm delay line and Lecroy TDC linked to a mass semiconductor memory of 512 x 256 elements. The experiment will be controlled by a PDP 11/04 computer with 28 K memory interfaced to a CAMAC create with 64 K fast access CAMAC memory. The system should be relatively easy to use with good order to order resolution and reasonable rate for small angle diffraction and scattering experiments on biological systems. Evaluation of the set-up for protein crystallography is planned though a TV based image intensifier (Enraf-Nonius) is preferred for this application at the SRS. (orig.)

  9. Synchrotron X-Ray Radiation and Deformation Studies

    DEFF Research Database (Denmark)

    Fæster Nielsen, Søren

    In the present thesis two different synchrotron X-ray diffraction techniques capable of producing non-destructive information from the bulk of samples, have been investigated. Traditionally depth resolu-tion in diffraction experiments is obtained by inserting pinholes in both the incoming...... machining. The conical slit has six 25µm thick conically shaped openings matching six of the Debye-Scherrer cones from a fcc powder. By combining the conical slit with a micro-focused incoming beam of hard X-rays an embedded gauge volume is defined. Using a 2D detector, fast and complete information can...... boundary morphology. Another X-ray diffraction technique was applied on the three-dimensional X-ray diffraction (3DXRD) microscope at the ESRF synchrotron. The microscope uses a new technique based on ray tracing of diffracted high energy X-rays, providing a fast and non-destructive scheme for mapping...

  10. Texture correction in neutron powder diffraction data of molybdite using the generalized spherical harmonic model

    Science.gov (United States)

    Sitepu, H.; O'Connor, B. H.; Benmarouane, A.; Hansen, T.; Ritter, C.; Brokmeier, H.-G.

    2004-07-01

    Texture correction of isostatically pressed molybdite powders has been carried out using the D1A high-resolution fixed wavelength 25-detector powder diffractometer at the Institut Laue-Langevin. All of the samples were spun during the data collections to improve particle statistics. In the present study, the GSAS Rietveld program was used for analysis of each pattern, in which the generalized spherical harmonic (GSH) is generated using selection rules depending on the crystal symmetry of the phase under investigation. The default sample texture symmetry was chosen to be cylindrical and the maximum of eight harmonic orders was selected. The results indicate that the correct crystal structure can be obtained when applying corrections to intensities using the GSH description.

  11. Static tensile deformation behavior of a lean duplex stainless steel studied by in situ neutron diffraction and synchrotron radiation white x-rays

    International Nuclear Information System (INIS)

    Tsuchida, Noriyuki; Kawahata, Taiji; Ishimaru, Eiichiro; Takahashi, Akihiko; Suzuki, Hiroshi; Shobu, Takahisa

    2013-01-01

    To investigate the tensile deformation behavior of a lean duplex stainless steel (S32101) from the viewpoints of plastic deformability among phases or grains, we performed static tensile tests, in situ neutron diffraction, and white x-ray diffraction experiments at room temperature. In the static tensile tests, the S32101 steel displayed a larger uniform elongation and a better tensile strength-uniform elongation balance than a commercial SUS329J4L duplex stainless steel. A larger uniform elongation of S32101 is associated with the macroscopic work hardening behavior that a work hardening rate higher than the flow stress can maintain up until high true strains. From the experimental results of synchrotron radiation white x-ray diffraction experiments, the hard phase of S32101 was changed from the ferrite (α) phase to austenite (γ) one during tensile deformation. This led to a larger stress partitioning between the phases at the latter stage of deformation. From the experimental results of in situ neutron diffraction, it was found that the stress partitioning of the γ phase in the S32101 was the largest among the present results. Therefore, the larger work hardening rate of S32101 can be explained by the large stress partitioning of the γ phase, that between γ and α phases and γ volume fraction. (author)

  12. Neutron diffraction measurements of residual stress in a powder metallurgy component

    International Nuclear Information System (INIS)

    Schneider, L.C.R.; Hainsworth, S.V.; Cocks, A.C.F.; Fitzpatrick, M.E.

    2005-01-01

    Residual stresses in a typical industrial green component were determined using neutron diffraction. The measured residual stresses were found to correlate with cross-sectional variations. Residual stress at the edge of the compact in contact with the die wall during compaction reached up to +80 MPa (tension) and -100 MPa (compression)

  13. Synchrotron radiation: earth, environmental and materials sciences applications

    International Nuclear Information System (INIS)

    Henderson, G.; Baker, D.R.

    2002-01-01

    Mineralogical Association of Canada Short Course 30 called Synchrotron Radiation: Earth, Environmental and Materials Sciences Applications was held in Saskatoon, Saskatchewan in 2002. This short course attempts to introduce to the general earth science community some of the basics of synchrotron radiation-based research. It is not intended as a review of all aspects of every synchrotron-based technique, although it does include the important literature into which knowledge of more specific areas can be gained. Instead, it covers the basics of synchrotron research at a level suitable for those interested in beginning to use synchrotron radiation in their research. Chapter 1 covers the physics of synchrotron radiation and synchrotron storage rings in general. Chapter 2 details what the Canadian Light Source is, what it will be capable of, and the types of experiments that will be able to be performed on the beamlines. Chapter 3 covers the basics of synchrotron-based diffraction studies including both powder and single crystal studies. Chapter 4 introduces the novice user to X-ray absorption spectroscopy (EXAFS/XANES) and includes details on how to correctly reduce the data. Chapter 5 outlines the capabilities of the X-ray microprobe for chemical analyses, micro-EXAFS/XANES and imaging of geological samples. Chapter 6 gives a detailed overview of synchrotron-based X-ray photoelectron spectroscopy with application to mineralogical and geochemical studies. Finally, chapter 7 introduces the types of experiments within the geological community that are commonly performed on amorphous materials

  14. Polarized neutron diffraction by D sub 2 chemisorbed on a nickel powder

    Energy Technology Data Exchange (ETDEWEB)

    Beaufils, J.P. (Inst. Laue-Langevin, 38 - Grenoble (France))

    1992-02-01

    The theory of surface differential diffraction (SDD) is extended to the case of polarized neutron diffraction. Nuclear and magnetic surface contributions are thus separated. A method for coherent description of the geometry of the grains is proposed. A saturated D layer chemisorbed on Ni carried by silica is studied with the following results: (111) faces represent the majority of the surface; D atoms sit above the centers of surface Ni triangles with no Ni atom in the underlying layer, the Ni-D distance is equal to 0.215(7) nm; the magnetic-moment modification induced by chemisorption is mainly localized in the surface layer of nickel. Two possible interpretations of the magnetic structure factor are discussed: One assumes no magnetic moment on D atoms but Ni displacements; the other is based on opposite assumptions. (orig.).

  15. Structure refinement of (Sr,Ba)Nb2O6 ceramic powder from neutron and X-Ray diffraction data

    International Nuclear Information System (INIS)

    Carrio, J.G.; Mascarenhas, Y.P.; Yelon, W.; Santos, I.A.; Garcia, D.; Eiras, J.A.

    2002-01-01

    The structure of polycrystalline strontium barium niobate at room temperature was refined by the Rietveld method. Sintered ceramic samples were used to collect powder neutron and X-ray diffraction data. The ratio Sr/Ba ∼ 64/36 was found from the initial batch composition Sr 0 .61 Ba 0.39 Nb 2 O 6 , corroborating with the quantitative X-ray dispersive spectroscopy (EDS) measurements. The structure is tetragonal with cell parameters a, b 12.4504(3) Angstrom and c = 3.9325(1) Angstrom and space group P4bm. It was not necessary to introduce any positional disorder for the oxygen atoms. Cation Nb +5 displacements not parallel to the c direction are presented, which can influence the behavior of the ferroelectric properties. (author)

  16. High-temperature dehydration of talc: a kinetics study using in situ X-ray powder diffraction

    Science.gov (United States)

    Wang, Duojun; Yi, Li; Huang, Bojin; Liu, Chuanjiang

    2015-06-01

    High-temperature in situ X-ray powder diffraction patterns were used to study the dehydration kinetics of natural talc with a size of 10-15 µm. The talc was annealed from 1073 to 1223 K, and the variations in the characteristic peaks corresponding to talc with the time were recorded to determine the reaction progress. The decomposition of talc occurred, and peaks corresponding to talc and peaks corresponding to enstatite and quartz were observed. The enstatite and talc exhibited a topotactic relationship. The dehydration kinetics of talc was studied as a function of temperature between 1073 and 1223 K. The kinetics data could be modeled using an Avrami equation that considers nucleation and growth processes ? where n varies from 0.4 to 0.8. The rate constant (k) equation for the natural talc is ? The reaction mechanism for the dehydration of talc is a heterogeneous nucleation and growth mechanism.

  17. Kinetics of thermal decomposition of titanium hydride powder using in situ high-temperature X-ray diffraction (HTXRD

    Directory of Open Access Journals (Sweden)

    Hugo Ricardo Zschommler Sandim

    2005-09-01

    Full Text Available The thermal decomposition of titanium hydride powder (delta-phase to titanium (alpha-phase was investigated by means of thermogravimetric analysis (TGA and high-temperature X-ray diffraction (HTXRD in high vacuum. The delta-to-alpha phase transformation was followed in situ by HTXRD at temperatures varying from room temperature up to 1000 °C. The transformation was also analyzed as a function of time at isothermal conditions from 450 to 650 °C. The results of TGA show that the decomposition of the titanium hydride becomes significant at about 450 °C. Above 500 °C the decomposition is completed in times shorter than 50 minutes. The apparent activation energy for hydrogen desorption was found to be 63 ± 6 kJ.mol-1.

  18. Neutron powder diffraction study of the infinite-layer compounds Sr1-xNdxCuO2

    International Nuclear Information System (INIS)

    Bobrovskii, V.; Mirmelstein, A.; Podlesnyak, A.; Zhdakhin, I.; Goshchitskii, B.; Mitberg, E.; Khlybov, E.; Fauth, F.; Furrer, A.

    1997-01-01

    The infinite-layer (IL) systems have rather simple crystal structures and thereby offer an ideal system for an improved understanding of the phenomenon of high-T c superconductivity. The production of IL compounds is by no means trivial, since the synthesis of single-phase material requires both high pressures and high temperatures. The infinite-layer compounds of the (Sr,Ln)CuO 2 family have been prepared by a new synthesis method from the low-pressure phase of SrCuO 2 and NdCuO 2 as starting materials. The actual rare-earth content in the IL phase is shown to depend on both temperature and pressure. Crystal structure of the IL samples have been studied using neutron powder diffraction and X-ray measurements. (orig.)

  19. Structure Refinement of (Sr,BaNb2O6 Ceramic Powder from Neutron and X-Rays Diffraction Data

    Directory of Open Access Journals (Sweden)

    J.G. Carrio

    2002-03-01

    Full Text Available The structure of polycrystalline strontium barium niobate at room temperature was refined by the Rietveld method. Sintered ceramic samples were used to collect powder neutron and X-ray diffraction data. The ratio Sr/Ba ~ 64/36 was found from the initial batch composition Sr0.61Ba0.39Nb2O6, corroborating with the quantitative X-ray dispersive spectroscopy (EDS measurements. The structure is tetragonal with cell parameters a, b = 12.4504(3 Å and c = 3.9325(1 Å and space group P4bm. It was not necessary to introduce any positional disorder for the oxygen atoms. Cation Nb+5 displacements not parallel to the c direction are presented, which can influence the behavior of the ferroelectric properties.

  20. Homogeneity characterisation of (U,Gd)O2 sintered pellets by X-ray diffraction powder analysis applying Rietveld method

    International Nuclear Information System (INIS)

    Leyva, Ana G.; Vega, Daniel R.; Trimarco, Veronica G.; Marchi, Daniel E.

    1999-01-01

    The (U,Gd)O 2 sintered pellets are fabricated by different methods. The homogeneity characterisation of Gd content seems to be necessary as a production control to qualify the process and the final product. The micrographic technique is the most common method used to analyse the homogeneity of these samples, this method requires time and expertise to obtain good results. In this paper, we propose an analysis of the X-ray diffraction powder patterns through the Rietveld method, in which the differences between the experimental data and the calculated from a crystalline structure model proposed are evaluated. This result allows to determine the cell parameters, that can be correlated with the Gd concentration, and the existence of other phases with different Gd ratio. (author)

  1. Structural study, by surface differential diffraction of neutrons, of the surface of a nickel powder covered with deuterium

    Science.gov (United States)

    Beaufils, J. P.

    1993-01-01

    The analysis of the data of a neutron surface differential diffraction experiment, using H positions determined in the literature whenever available, supports the following model: Grains of the studied nickel powder are limited by (20 ± 10)% of (111) faces and 80% of (110) faces. The (110) faces expose (111) and (1¯11) facets because of anisotropic roughening. A new interpretation of the streaks observed in LEED patterns and a discussion of the coverage provides additional arguments in favour of the roughening. On the facets of the rough faces, the D atoms are displaced from the position they would have on a genuine (111) face. They are no longer on a C3 axis. The Ni atoms of the rough faces suffer an average displacement of 0.015 ± 0.015 nm in the [110] outward direction. The shortest NiD distance on the rough face is equal to 0.19 ± 0.015 nm.

  2. (Na,□)5[MnO2]13 nanorods: a new tunnel structure for electrode materials determined ab initio and refined through a combination of electron and synchrotron diffraction data

    Science.gov (United States)

    Mugnaioli, Enrico; Gemmi, Mauro; Merlini, Marco; Gregorkiewitz, Michele

    2016-01-01

    (Nax□1 − x)5[MnO2]13 has been synthesized with x = 0.80 (4), corresponding to Na0.31[MnO2]. This well known material is usually cited as Na0.4[MnO2] and is believed to have a romanèchite-like framework. Here, its true structure is determined, ab initio, by single-crystal electron diffraction tomography (EDT) and refined both by EDT data applying dynamical scattering theory and by the Rietveld method based on synchrotron powder diffraction data (χ2 = 0.690, R wp = 0.051, R p = 0.037, R F2 = 0.035). The unit cell is monoclinic C2/m, a = 22.5199 (6), b = 2.83987 (6), c = 14.8815 (4) Å, β = 105.0925 (16)°, V = 918.90 (4) Å3, Z = 2. A hitherto unknown [MnO2] framework is found, which is mainly based on edge- and corner-sharing octahedra and comprises three types of tunnels: per unit cell, two are defined by S-shaped 10-rings, four by egg-shaped 8-rings, and two by slightly oval 6-rings of Mn polyhedra. Na occupies all tunnels. The so-determined structure excellently explains previous reports on the electrochemistry of (Na,□)5[MnO2]13. The trivalent Mn3+ ions concentrate at two of the seven Mn sites where larger Mn—O distances and Jahn–Teller distortion are observed. One of the Mn3+ sites is five-coordinated in a square pyramid which, on oxidation to Mn4+, may easily undergo topotactic transformation to an octahedron suggesting a possible pathway for the transition among different tunnel structures. PMID:27910840

  3. Solid state characterization and crystal structure from X-ray powder diffraction of two polymorphic forms of ranitidine base.

    Science.gov (United States)

    de Armas, Héctor Novoa; Peeters, Oswald M; Blaton, Norbert; Van Gyseghem, Elke; Martens, Johan; Van Haele, Gerrit; Van Den Mooter, Guy

    2009-01-01

    Ranitidine hydrochloride (RAN-HCl), a known anti-ulcer drug, is the product of reaction between HCl and ranitidine base (RAN-B). RAN-HCl has been extensively studied; however this is not the case of the RAN-B. The solid state characterization of RAN-B polymorphs has been carried out using different analytical techniques (microscopy, thermal analysis, Fourier transform infrared spectrometry in the attenuated total reflection mode, (13)C-CPMAS-NMR spectroscopy and X-ray powder diffraction). The crystal structures of RAN-B form I and form II have been determined using conventional X-ray powder diffraction in combination with simulated annealing and whole profile pattern matching, and refined using rigid-body Rietveld refinement. RAN-B form I is a monoclinic polymorph with cell parameters: a = 7.317(2), b = 9.021(2), c = 25.098(6) A, beta = 95.690(1) degrees and space group P2(1)/c. The form II is orthorhombic: a = 31.252(4), b = 13.052(2), c = 8.0892(11) A with space group Pbca. In RAN-B polymorphs, the nitro group is involved in a strong intramolecular hydrogen bond responsible for the existence of a Z configuration in the enamine portion of the molecules. A tail to tail packing motif can be denoted via intermolecular hydrogen bonds. The crystal structures of RAN-B forms are compared to those of RAN-HCl polymorphs. RAN-B polymorphs are monotropic polymorphic pairs. (c) 2008 Wiley-Liss, Inc. and the American Pharmacists Association

  4. Validation of molecular crystal structures from powder diffraction data with dispersion-corrected density functional theory (DFT-D).

    Science.gov (United States)

    van de Streek, Jacco; Neumann, Marcus A

    2014-12-01

    In 2010 we energy-minimized 225 high-quality single-crystal (SX) structures with dispersion-corrected density functional theory (DFT-D) to establish a quantitative benchmark. For the current paper, 215 organic crystal structures determined from X-ray powder diffraction (XRPD) data and published in an IUCr journal were energy-minimized with DFT-D and compared to the SX benchmark. The on average slightly less accurate atomic coordinates of XRPD structures do lead to systematically higher root mean square Cartesian displacement (RMSCD) values upon energy minimization than for SX structures, but the RMSCD value is still a good indicator for the detection of structures that deserve a closer look. The upper RMSCD limit for a correct structure must be increased from 0.25 Å for SX structures to 0.35 Å for XRPD structures; the grey area must be extended from 0.30 to 0.40 Å. Based on the energy minimizations, three structures are re-refined to give more precise atomic coordinates. For six structures our calculations provide the missing positions for the H atoms, for five structures they provide corrected positions for some H atoms. Seven crystal structures showed a minor error for a non-H atom. For five structures the energy minimizations suggest a higher space-group symmetry. For the 225 SX structures, the only deviations observed upon energy minimization were three minor H-atom related issues. Preferred orientation is the most important cause of problems. A preferred-orientation correction is the only correction where the experimental data are modified to fit the model. We conclude that molecular crystal structures determined from powder diffraction data that are published in IUCr journals are of high quality, with less than 4% containing an error in a non-H atom.

  5. Microstructure evolution in copper under severe plastic deformation detected by in situ X-ray diffraction using monochromatic synchrotron light

    Energy Technology Data Exchange (ETDEWEB)

    Kilmametov, A.R. [Institute of Physics of Advanced Materials, Ufa State Aviation Technical University, K. Marx St. 12, Ufa 450000 (Russian Federation); Vaughan, G. [European Synchrotron Radiation Facilities ESRF, Grenoble (France); Yavari, A.R.; LeMoulec, A. [Euronano, LTPCM-CNRS umr 5614, Institut National Polytechnique de Grenoble, 38402 St-Martin-d' Heres (France); Botta, W.J. [Depto. Engenharia de Materiais, Universidade Federal de Sao Carlos (UFSCar), SP, Brazil. 3UNIVA, Av. Shishima Hifumi, 2911 Sao Jose dos Campos, SP (Brazil); Valiev, R.Z. [Institute of Physics of Advanced Materials, Ufa State Aviation Technical University, K. Marx St. 12, Ufa 450000 (Russian Federation)], E-mail: rzvaliev@mail.rb.ru

    2009-03-15

    Microstructure evolution in severely deformed Cu has been investigated using high-energy synchrotron light during in situ high-pressure torsion (HPT) at room temperature. Relative changes in broadening of Bragg peaks and crystal lattice expansion were studied in the loading-unloading regime of torsion straining. Experimental results revealed fast relaxation (on the order of hundred of seconds) that occurred due to annihilation of HPT-induced crystal lattice defects, which were generated directly during deformation. The kinetics of relaxation is probably diffusion-controlled; therefore, the enhanced diffusivity can be explained by extremely high excess vacancy concentration, which is usually achieved at thermal equilibrium near the melting point.

  6. Photoelectron diffraction study and structure determination of ultrathin hafnium silicide layers on silicon(1 0 0) using Mg K{alpha} radiation and synchrotron light

    Energy Technology Data Exchange (ETDEWEB)

    Fluechter, C.R. [Experimentelle Physik 1, Universitaet Dortmund, Otto-Hahn-Str. 4, D-44221 Dortmund (Germany); DELTA, Universitaet Dortmund, Maria-Goeppert-Mayer-Str. 2, D-44227 Dortmund (Germany)], E-mail: christian.fluechter@uni-dortmund.de; Siervo, A. de [Laboratorio Nacional de Luz Sincrotron, C.P. 6192, 13084-971 Campinas, SP (Brazil); Weier, D. [Experimentelle Physik 1, Universitaet Dortmund, Otto-Hahn-Str. 4, D-44221 Dortmund (Germany); DELTA, Universitaet Dortmund, Maria-Goeppert-Mayer-Str. 2, D-44227 Dortmund (Germany); Schuermann, M. [Experimentelle Physik 1, Universitaet Dortmund, Otto-Hahn-Str. 4, D-44221 Dortmund (Germany); Berges, U. [Experimentelle Physik 1, Universitaet Dortmund, Otto-Hahn-Str. 4, D-44221 Dortmund (Germany); DELTA, Universitaet Dortmund, Maria-Goeppert-Mayer-Str. 2, D-44227 Dortmund (Germany); Dreiner, S. [Experimentelle Physik 1, Universitaet Dortmund, Otto-Hahn-Str. 4, D-44221 Dortmund (Germany); Carazzolle, M.F. [Instituto de Fisica, Universidade Estadual de Campinas, C.P. 6165, 13083-970 Campinas, SP (Brazil); Landers, R. [Laboratorio Nacional de Luz Sincrotron, C.P. 6192, 13084-971 Campinas, SP (Brazil); Instituto de Fisica, Universidade Estadual de Campinas, C.P. 6165, 13083-970 Campinas, SP (Brazil); Kleiman, G.G. [Instituto de Fisica, Universidade Estadual de Campinas, C.P. 6165, 13083-970 Campinas, SP (Brazil); Westphal, C. [Experimentelle Physik 1, Universitaet Dortmund, Otto-Hahn-Str. 4, D-44221 Dortmund (Germany); DELTA, Universitaet Dortmund, Maria-Goeppert-Mayer-Str. 2, D-44227 Dortmund (Germany)

    2007-05-15

    In order to increase the switching speed and the efficiency of modern semiconductor devices a further down scaling is desired. Thus, the SiO{sub 2} gate dielectric might be replaced by layers of a material with a much higher dielectric constant like HfO{sub 2}. A major problem of the system HfO{sub 2}/Si(1 0 0) is the silicidation of hafnium at the interface. Therefore, ultrathin films (3-30 A) of HfSi{sub 2} on Si(1 0 0) were investigated by photoelectron spectroscopy, low-energy electron diffraction and X-ray photoelectron diffraction. Synchrotron light with an energy of h{nu} = 180 eV was used for excitation. First results were obtained using a Mg X-ray tube (h{nu} = 1253.6 eV). In order to determine the structure of the films, the recorded photoelectron diffraction patterns were compared to computer simulations of model structures. The simulations for the low-energy measurements were performed using the program MSPHD. As a result a modified zirconium silicide structure is presented in order to describe the structure of ultrathin HfSi{sub 2} films on Si(1 0 0)

  7. The Molecular Architecture for the Intermediate Filaments of Hard [alpha]-Keratin Based on the Superlattice Data Obtained from a Study ofMammals Using Synchrotron Fibre Diffraction

    Energy Technology Data Exchange (ETDEWEB)

    James, Veronica (ANU)

    2014-09-24

    High- and low-angle X-ray diffraction studies of hard {alpha}-keratin have been studied, and various models have been proposed over the last 70 years. Most of these studies have been confined to one or two forms of alpha keratin. This high- and low-angle synchrotron fibre diffraction study extends the study to cover all available data for all known forms of hard {alpha}-keratin including hairs, fingernails, hooves, horn, and quills from mammals, marsupials, and a monotreme, and it confirms that the model proposed is universally acceptable for all mammals. A complete Bragg analysis of the meridional diffraction patterns, including multiple-time exposures to verify any weak reflections, verified the existence of a superlattice consisting of two infinite lattices and three finite lattices. An analysis of the equatorial patterns establishes the radii of the oligomeric levels of dimers, tetramers, and intermediate filaments (IFs) together with the centre to centre distance for the IFs, thus confirming the proposed helices within helices molecular architecture for hard {alpha}-keratin. The results verify that the structure proposed by Feughelman and James meets the criteria for a valid {alpha}-keratin structure.

  8. About some practical aspects of X-ray diffraction : From single crystal to powders

    Energy Technology Data Exchange (ETDEWEB)

    Giacovazzo, C. [Bari Univ. (Italy). Dip. Geomineralogico

    1996-09-01

    An ideal polycrystalline material or power is an ensemble of a very large number of randomly oriented crystallites. It is shown the effect that this random orientation has on the diffraction of a specimen assumed to contain only one reciprocal lattice node. The most remarkable difference with the single-crystal case is that now must think of scattering vectors not as lying on discrete nodes of reciprocal lattice vectors, the distances from the single-crystal reciprocal lattice nodes to the origin of reciprocal space.

  9. Neutron powder diffraction study on the iron-based nitride superconductor ThFeAsN

    Science.gov (United States)

    Mao, Huican; Wang, Cao; Maynard-Casely, Helen E.; Huang, Qingzhen; Wang, Zhicheng; Cao, Guanghan; Li, Shiliang; Luo, Huiqian

    2017-03-01

    We report neutron diffraction and transport results on the newly discovered superconducting nitride ThFeAsN with T_c= 30 \\text{K} . No magnetic transition, but a weak structural distortion around 160 K, is observed by cooling from 300 K to 6 K. Analysis on the resistivity, Hall transport and crystal structure suggests that this material behaves as an electron optimally doped pnictide superconductor due to extra electrons from nitrogen deficiency or oxygen occupancy at the nitrogen site, which, together with the low arsenic height, may enhance the electron itinerancy and reduce the electron correlations, thus suppressing the static magnetic order.

  10. Crystal structure of CuFe{sub 2}InSe{sub 4} from X-ray powder diffraction

    Energy Technology Data Exchange (ETDEWEB)

    Delgado, G.E. [Laboratorio de Cristalografia, Departamento de Quimica, Facultad de Ciencias, Universidad de Los Andes, Merida 5101 (Venezuela)], E-mail: gerzon@ula.ve; Mora, A.J. [Laboratorio de Cristalografia, Departamento de Quimica, Facultad de Ciencias, Universidad de Los Andes, Merida 5101 (Venezuela); Grima-Gallardo, P.; Quintero, M. [Centro de Estudio de Semiconductores, Departamento de Fisica, Facultad de Ciencias, Universidad de Los Andes, Merida 5101 (Venezuela)

    2008-04-24

    The crystal structure of the semiconductor compound CuFe{sub 2}InSe{sub 4} was analyzed using X-ray powder diffraction data. The powder pattern refined by the Rietveld method was composed of 86.6% of the principal phase CuFe{sub 2}InSe{sub 4} and 13.4% of the binary phase FeSe. CuFe{sub 2}InSe{sub 4} crystallizes in the tetragonal space group I4-bar2m (no. 121), Z = 2, with unit cell parameters a = 5.7694(3) A, c = 11.495(1) A, V = 382.62(4) A{sup 3}. FeSe crystallizes in the tetragonal space group P4/nmm (no. 129), Z = 2, and a = 3.784(1) A, c 5.502(2) A, V = 78.78(4) A{sup 3}. The refinement of 28 instrumental and structural parameters led to R{sub p} = 8.2%, R{sub wp} = 10.7%, R{sub exp} = 6.7% and S = 1.7; R{sub B} = 9.9% (CuFe{sub 2}InSe{sub 4}), R{sub B} = 8.8% (FeSe) for 76 and 36 independent reflections, respectively.

  11. Preparation and Crystal Structures of Some AIVB2IIO4 Compounds: Powder X-Ray Diffraction and Rietveld Analysis

    Directory of Open Access Journals (Sweden)

    K. Jeyadheepan

    2014-01-01

    Full Text Available The AIVB2IIO4 compounds such as cadmium tin oxide (Cd2SnO4 or CTO and zinc tin oxide (Zn2SnO4 or ZTO are synthesized by solid state reaction of the subsequent binary oxides. The synthesized powders were analyzed through the powder X-ray diffraction (PXRD. Cell search done on the PXRD patterns shows that the Cd2SnO4 crystallizes in orthorhombic structure with space group Pbam and the cell parameters as a=5.568(2 Å, b=9.894(3 Å, and c=3.193(1 Å and the Zn2SnO4 crystallizes as cubic with the space group Fd3 -m and with the cell parameter a=8.660(2 Å. Rietveld refinement was done on the PXRD patterns to get the crystal structure of the Cd2SnO4 and Zn2SnO4 and to define the site deficiency of atoms which causes the electrical properties of the materials.

  12. Residual stress state in an induction hardened steel bar determined by synchrotron- and neutron diffraction compared to results from lab-XRD

    Energy Technology Data Exchange (ETDEWEB)

    Holmberg, Jonas, E-mail: jonas.holmberg@swerea.se [Swerea IVF AB, Argongatan 30, 431 22 Mölndal (Sweden); University West, 461 86 Trollhättan (Sweden); Steuwer, Axel [Nelson Mandela Metropolitan University, Gardham Avenue, 6031 Port Elizabeth (South Africa); Stormvinter, Albin; Kristoffersen, Hans [Swerea IVF AB, Argongatan 30, 431 22 Mölndal (Sweden); Haakanen, Merja [Stresstech OY, Tikkutehtaantie 1, 40 800 Vaajakoski (Finland); Berglund, Johan [Swerea IVF AB, Argongatan 30, 431 22 Mölndal (Sweden)

    2016-06-14

    Induction hardening is a relatively rapid heat treatment method to increase mechanical properties of steel components. However, results from FE-simulation of the induction hardening process show that a tensile stress peak will build up in the transition zone in order to balance the high compressive stresses close to the surface. This tensile stress peak is located in the transition zone between the hardened zone and the core material. The main objective with this investigation has been to non-destructively validate the residual stress state throughout an induction hardened component. Thereby, allowing to experimentally confirming the existence and magnitude of the tensile stress peak arising from rapid heat treatment. For this purpose a cylindrical steel bar of grade C45 was induction hardened and characterised regarding the microstructure, hardness, hardening depth and residual stresses. This investigation shows that a combined measurement with synchrotron/neutron diffraction is well suited to non-destructively measure the strains through the steel bar of a diameter of 20 mm and thereby making it possible to calculate the residual stress profile. The result verified the high compressive stresses at the surface which rapidly changes to tensile stresses in the transition zone resulting in a large tensile stress peak. Measured stresses by conventional lab-XRD showed however that at depths below 1.5 mm the stresses were lower compared to the synchrotron and neutron data. This is believed to be an effect of stress relaxation from the layer removal. The FE-simulation predicts the depth of the tensile stress peak well but exaggerates the magnitude compared to the measured results by synchrotron/neutron measurements. This is an important knowledge when designing the component and the heat treatment process since this tensile stress peak will have great impact on the mechanical properties of the final component.

  13. Residual stress state in an induction hardened steel bar determined by synchrotron- and neutron diffraction compared to results from lab-XRD

    International Nuclear Information System (INIS)

    Holmberg, Jonas; Steuwer, Axel; Stormvinter, Albin; Kristoffersen, Hans; Haakanen, Merja; Berglund, Johan

    2016-01-01

    Induction hardening is a relatively rapid heat treatment method to increase mechanical properties of steel components. However, results from FE-simulation of the induction hardening process show that a tensile stress peak will build up in the transition zone in order to balance the high compressive stresses close to the surface. This tensile stress peak is located in the transition zone between the hardened zone and the core material. The main objective with this investigation has been to non-destructively validate the residual stress state throughout an induction hardened component. Thereby, allowing to experimentally confirming the existence and magnitude of the tensile stress peak arising from rapid heat treatment. For this purpose a cylindrical steel bar of grade C45 was induction hardened and characterised regarding the microstructure, hardness, hardening depth and residual stresses. This investigation shows that a combined measurement with synchrotron/neutron diffraction is well suited to non-destructively measure the strains through the steel bar of a diameter of 20 mm and thereby making it possible to calculate the residual stress profile. The result verified the high compressive stresses at the surface which rapidly changes to tensile stresses in the transition zone resulting in a large tensile stress peak. Measured stresses by conventional lab-XRD showed however that at depths below 1.5 mm the stresses were lower compared to the synchrotron and neutron data. This is believed to be an effect of stress relaxation from the layer removal. The FE-simulation predicts the depth of the tensile stress peak well but exaggerates the magnitude compared to the measured results by synchrotron/neutron measurements. This is an important knowledge when designing the component and the heat treatment process since this tensile stress peak will have great impact on the mechanical properties of the final component.

  14. Neutron powder thermo-diffraction in mechanically alloyed Fe{sub 64}Ni{sub 36} invar alloy

    Energy Technology Data Exchange (ETDEWEB)

    Gorria, Pedro, E-mail: pgorria@uniovi.e [Departamento de Fisica, Universidad de Oviedo, Avda. Calvo Sotelo s/n, Oviedo 33007, Asturias (Spain); Martinez-Blanco, David [Unidad de Magnetometria, SCT' s, Universidad de Oviedo, Julian Claveria 8, 33006 Oviedo (Spain); Blanco, Jesus A. [Departamento de Fisica, Universidad de Oviedo, Avda. Calvo Sotelo s/n, Oviedo 33007, Asturias (Spain); Smith, Ronald I. [ISIS Facility, RAL, Chilton, Didcot, Oxon OX11 0QX (United Kingdom)

    2010-04-16

    Nanostructured Fe{sub 64}Ni{sub 36} alloy has been obtained using high-energy ball milling for 35 h of milling time, Fe{sub 64}Ni{sub 36} MA-35 h. The initial as-milled Fe{sub 64}Ni{sub 36} MA-35 h powders are inhomogeneous, showing a majority phase with a face-centred cubic (fcc) crystal structure [88(2)%] and a minority phase with body-centred cubic (bcc) crystal structure [7(2)%]. The evolution of the microstructure with temperature between 300 K and 1100 K has been followed by means of in situ neutron powder thermo-diffraction experiments. The room temperature values for the mean crystalline size and the mechanical-induced microstrain of the fcc phase in the as-milled sample are {approx}10 nm and {approx}0.7%, respectively. Moreover, after heating the Fe{sub 64}Ni{sub 36} MA-35 h powders up to 1100 K, an increase of around 65 K in the Curie temperature respect to that of the commercial coarse-grained alloy of the same composition is observed. The latter together with the observed temperature dependence of the lattice parameter suggests that the Fe{sub 64}Ni{sub 36} MA-35 h sample subjected to the heating process exhibits invar behaviour. On heating up to 1100 K thermal relaxation of the microstructure occurs giving rise to grain growth above 100 nm, nearly vanishing values for the maximum strain, and the transformation of the bcc phase into the fcc one above 800 K, being the latter stable in subsequent heating-cooling processes.

  15. Investigation of recrystallization of amorphous trehalose through hot-humidity stage X-ray powder diffraction.

    Science.gov (United States)

    Jójárt-Laczkovich, Orsolya; Katona, Gábor; Aigner, Zoltán; Szabó-Révész, Piroska

    2016-12-01

    The aim of this work was an investigation of the physical changes of the amorphous model material spray-dried trehalose through the use of various analytical techniques and to identify a suitable, rapid method able to quantify the changes. The crystallinity changes and recrystallization process of amorphous samples were investigated by hot-humidity stage X-ray powder diffractometry (HH-XRPD) with fresh samples, conventional X-ray powder diffractometry (XRPD) used stored samples and by differential scanning calorimetry (DSC). The data from the three methods were compared and the various forms of trehalose were analysed. HH-XRPD demonstrated that the recrystallization began at 40 and 60°C up to 45% RH and at 70°C up to 30% RH into dihydrate form. At 70°C up to 60% RH the anhydrous form of trehalose appeared too. Conventional XRPD results showed, that in the 28days stored samples the dihydrate form was detected at 40°C, 50% RH. Storage at 60°C, 40% RH resulted in the appearance of the anhydrous form and at 60°C, 50% RH both polymorphic forms were detected. By carrying out the DSC measurements at different temperatures the fraction of recrystallized trehalose dihydrate was detected. The recrystallization investigated by HH-XRPD and DSC followed Avrami kinetics, the calculated rate constants of isothermal crystallization (K) were same. Both HH-XRPD and conventional XRPD was suitable for the detection of the physical changes of the amorphous model material. DSC measurements showed similar results as HH-XRPD. Primarily HH-XRPD could be suggested for prediction, because the method is fast and every changes could be studied on one sample. Copyright © 2016 Elsevier B.V. All rights reserved.

  16. Unusual thermal expansion of Sr{sub 2}IrO{sub 4}: A variable temperature synchrotron X-ray diffraction study

    Energy Technology Data Exchange (ETDEWEB)

    Ranjbar, Ben; Kennedy, Brendan J.

    2015-12-15

    The structure of Sr{sub 2}IrO{sub 4} has been studied between 20 and 1273 K using synchrotron X-ray diffraction. Sr{sub 2}IrO{sub 4} undergoes an apparently continuous transition from I4{sub 1}/acd to I4/mmm near 1123 K. The cooperative tilting of the corner sharing IrO{sub 6} octahedra in I4{sub 1}/acd results in highly anisotropic and unusual thermal expansion behavior with negative thermal expansion along the c-axis. - Graphical abstract: The progressive reduction in the magnitude of the tilting of the corner sharing IrO{sub 6} octahedra in Sr{sub 2}IrO{sub 4} results in negative thermal expansion along the c-axis before undergoing an apparently continuous transition from I4{sub 1}/acd to I4/mmm near 1123 K. - Highlights: • Thermal expansion of Sr{sub 2}IrO{sub 4} was studied using Synchrotron-XRD. • Unusual negative thermal expansion along c-axis observed. • I4{sub 1}/acd→I4/mmm phase transition detected near 1120 K. • Tilting of the corner sharing IrO{sub 6} octahedra related to the observed NTE.

  17. In situ X-ray diffraction of surface oxide on type 430 stainless steel in breakaway condition using synchrotron radiation

    Energy Technology Data Exchange (ETDEWEB)

    Saeki, Isao, E-mail: isaos@mmm.muroran-it.ac.jp [Department of Materials Science and Engineering, Muroran Institute of Technology, 27-1 Mizumoto, Muroran, Hokkaido 050-8585 (Japan); Sugiyama, Yusuke [Graduate School of Engineering, Muroran Institute of Technology, 27-1 Mizumoto, Muroran, Hokkaido 050-8585 (Japan); Hayashi, Shigenari; Yamauchi, Akira [Graduate School of Engineering, Hokkaido University, Kita 13 Nishi 8, Kita-ku, Sapporo, Hokkaido 006-8628 (Japan); Doi, Takashi; Nishiyama, Yoshitaka [Corporate R and D Laboratories, Sumitomo Metals Industries Ltd., 1-8 Fuso-cho, Amagasaki, Hyogo 660-0891 (Japan); Kyo, Shoji [Power Engineering R and D Centre, Kansai Electric Power Co., Inc., 3-11-20 Wakaoji, Amagasaki, Hyogo 661-0794 (Japan); Suzuki, Shigeru [Institute of Multidisciplinary Research for Advanced Materials, Tohoku University, 2-1-1 Katahira, Aoba-ku, Sendai, Miyagi 980-8577 (Japan); Sato, Masugu [Japan Synchrotron Radiation Research Institute, 1-1-1 Koto, Sayo-cho, Hyogo 679-5198 (Japan); Fujimoto, Shinji [Graduate School of Engineering, Osaka University, 2-1 Yamadaoka, Suita, Osaka 565-0871 (Japan)

    2012-02-15

    Highlights: Black-Right-Pointing-Pointer Breakaway studied with Synchrotron radiation X-ray. Black-Right-Pointing-Pointer Local equilibria between phases established during high-temperature oxidation. Black-Right-Pointing-Pointer Chemical failure model well describes the breakaway. - Abstract: Changes in the crystal structure of type 430 stainless steel and the oxides on its surface were studied in situ at 1373 K using a high-intensity synchrotron X-ray source provided by SPring-8 in Japan. The surface of the steel was initially covered with Cr{sub 2}O{sub 3}, which was then converted to FeCr{sub 2}O{sub 4}, and finally Fe{sub 3}O{sub 4} and Fe{sub 2}O{sub 3} formed on it. These results indicated that the reason for the breakaway oxidation in type 430 stainless steel is Cr depletion beneath Cr{sub 2}O{sub 3} layer and the subsequent ionisation of Fe, not the simple mechanical failure of Cr{sub 2}O{sub 3}.

  18. Investigations of the phase transition in V3O5 using energy dispersive X-ray diffraction and synchrotron radiation white beam X-ray topography

    International Nuclear Information System (INIS)

    Asbrink, S.; Gerward, L.; Staun Olsen, J.

    1985-01-01

    The reversible first order phase transition in V 3 O 5 at T t =155 0 C has been studied using a specially constructed oven, where the temperature can be kept constant within a few hundredths of a degree for several hours. Energy dispersive diffraction measurements have beem made in a temperature region around the phase transition with the fixed crystal method and the θ/2θ scanning method. White beam X-ray topographs have been obtained from the same crystal in the same temperature region using synchrotron radiation. The integrated intensities of the strong h 0 0 reflections show anomalies that are correlated with the corresponding X-ray topographs. Thus, an unexpected increase of crystal perfection is observed a few hundredths of a degree below T t . The energy dependence of the intensity maximum at T t for strong reflections has been determined and semi-quantitatively explained on the basis of extinction theory. (orig.)

  19. In situ synchrotron X-ray diffraction study of deformation behavior and load transfer in a Ti{sub 2}Ni-NiTi composite

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Junsong; Hao, Shijie; Yu, Cun; Shao, Yang; Ru, Yadong; Jiang, Daqiang; Cui, Lishan, E-mail: lscui@cup.edu.cn [Department of Materials Science and Engineering, China University of Petroleum-Beijing, Changping, Beijing 102249 (China); Liu, Yinong [School of Mechanical and Chemical Engineering, The University of Western Australia, Crawley, WA 6009 (Australia); Ren, Yang [X-ray Science Division, Argonne National Laboratory, Argonne, Illinois 60439 (United States); Huan, Yong [State Key Laboratory of Nonlinear Mechanics (LNM), Institute of Mechanics, Chinese Academy of Sciences, Beijing 100190 (China)

    2014-07-28

    The deformation behavior and load transfer of a dual-phase composite composed of martensite NiTi embedded in brittle Ti{sub 2}Ni matrices were investigated by using in situ synchrotron x-ray diffraction during compression. The composite exhibits a stage-wise deformation feature and a double-yielding phenomenon, which were caused by the interaction between Ti{sub 2}Ni and NiTi with alternative microscopic deformation mechanism. No load transfer occurs from the soft NiTi dendrites to the hard Ti{sub 2}Ni matrices during the pseudoplastic deformation (detwinning) of NiTi, which is significantly different from that previously reported in bulk metallic glasses matrices composites.

  20. Growth of magnesio-aluminate spinel in thin-film geometry: in situ monitoring using synchrotron X-ray diffraction and thermodynamic model

    Science.gov (United States)

    Götze, L. C.; Abart, R.; Milke, R.; Schorr, S.; Zizak, I.; Dohmen, R.; Wirth, R.

    2014-10-01

    Polycrystalline spinel layers were grown experimentally at the contacts between single-crystal corundum substrates and initially amorphous, then polycrystalline MgO thin films. The growth behavior of the spinel layers was monitored in situ using synchrotron X-ray diffraction. The change in the integrated intensity of the 111 spinel Bragg peak was correlated with the thickness of the layer as determined from ex situ TEM characterization of the run products. At a transition from linear growth, corresponding to interface reaction control, to parabolic growth, corresponding to diffusion control, occurred at a layer thickness of less than 10 nm. At 1,000 growth was largely linear up to a layer thickness in excess of 300 nm. A thermodynamic model was applied to extract the kinetic parameters characterizing interface motion and long-range diffusion from this growth behavior.

  1. Synchrotron high energy X-ray diffraction study of microstructure evolution of severely cold drawn NiTi wire during annealing

    Energy Technology Data Exchange (ETDEWEB)

    Yu, Cun; Aoun, Bachir; Cui, Lishan; Liu, Yinong; Yang, Hong; Jiang, Xiaohua; Cai, Song; Jiang, Daqiang; Liu, Zunping; Brown, Dennis E.; Ren, Yang

    2016-08-01

    Microstructure evolution of a cold-drawn NiTi shape memory alloy wire was investigated by means of in-situ synchrotron high-energy X-ray diffraction during continuous heating. The cold-drawn wire contained amorphous regions and nano-crystalline domains in its microstructure. Pair distribution function analysis revealed that the amorphous regions underwent structural relaxation via atomic rearrangement when heated above 100 °C. The nano-crystalline domains were found to exhibit a strong cold work induced lattice strain anisotropy having a preferential <111> fiber orientation along the wire axial direction. The lattice strain anisotropy systematically decreased upon heating above 200 °C, implying a structural recovery. A broad conical texture was formed in the wire specimen after crystallization similar in detail to the initial <111> texture axial orientation of the nano-crystalline domains produced by the severe cold wire drawing deformation.

  2. Crystal structure of CuFeInSe{sub 3} from X-ray powder diffraction data

    Energy Technology Data Exchange (ETDEWEB)

    Mora, Asiloe J.; Delgado, Gerzon E. [Laboratorio de Cristalografia, Departamento de Quimica, Facultad de Ciencias, Universidad de Los Andes, Merida 5101 (Venezuela); Grima-Gallardo, Pedro [Centro de Estudios de Semiconductores, Departamento de Fisica, Facultad de Ciencias, Universidad de Los Andes, Merida 5101 (Venezuela)

    2007-02-15

    The crystal structure of the adamantane compound CuFeInSe{sub 3}, belonging to the system (CuInSe{sub 2}){sub 1-x}(FeSe){sub x} with x=0.5, was analyzed using X-ray powder diffraction data. Several model structures were derived from the structure of the selenium rich phase CuInSe{sub 2.3} by permuting the cations in the available Wyckoff positions. The refinement of the best model by the Rietveld method in the tetragonal space group P anti 42c (N 112), Z=1, with unit cell parameters a=5.7762(2) Aa, c=11.5982(7) Aa and V=386.97(3) Aa{sup 3} led to R{sub p}=8.0%, R{sub wp}=9.6%, R{sub exp}=6.2% and {chi}{sup 2}=1.7 for 134 independent reflections. The model that best fitted the diffraction data has the following atomic distribution: Cu in Wyckoff site 2f; Fe in Wyckoff site 2d; In in Wyckoff site 2b and 1/3Cu, 1/3Fe, 1/3In in Wyckoff site 2f; Se in Wyckoff site 8n. (copyright 2007 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

  3. Complementing high-throughput X-ray powder diffraction data with quantum-chemical calculations: Application to piroxicam form III.

    Science.gov (United States)

    Naelapää, Kaisa; van de Streek, Jacco; Rantanen, Jukka; Bond, Andrew D

    2012-11-01

    High-throughput crystallisation and characterisation platforms provide an efficient means to carry out solid-form screening during the pre-formulation phase. To determine the crystal structures of identified new solid phases, however, usually requires independent crystallisation trials to produce single crystals or bulk samples of sufficient quantity to carry out high-quality X-ray diffraction measurements. This process could be made more efficient by a robust procedure for crystal structure determination directly from high-throughput X-ray powder diffraction (XRPD) data. Quantum-chemical calculations based on dispersion-corrected density functional theory (DFT-D) have now become feasible for typical small organic molecules used as active pharmaceutical ingredients. We demonstrate how these calculations can be applied to complement high-throughput XRPD data by determining the crystal structure of piroxicam form III. These combined experimental/quantum-chemical methods can provide access to reliable structural information in the course of an intensive experimentally based solid-form screening activity or in other circumstances wherein single crystals might never be viable, for example, for polymorphs obtained only during high-energy processing such as spray drying or milling. Copyright © 2012 Wiley Periodicals, Inc.

  4. The Crystal Structure of the Malaria Pigment Hemozoin as Elucidated by X-ray Powder Diffraction

    DEFF Research Database (Denmark)

    Straasø, Tine

    in the eradication of malaria. This thesis is a step towards that goal. When examining red blood cells from an infected person under a microscope dark pigment is observed. This dark pigment is actually small crystals called hemozoin. Hemozoin is a by-product formed by the parasite and a necessity for parasitic......Malaria is a widespread and severe disease caused by an infection by the parasite of the genus Plasmodium, the lifecycle of which is very complex. During its lifecycle the parasite resides in both a mosquito and a human host. If this cycle can be disrupted at any point, it will result...... survival. Successful inhibition of hemozoin crystallization will lead to parasitic death and thus break the cycle. The aim of this thesis is to elucidate the structure of hemozoin by means of X-ray diffraction techniques. Knowledge of the structure will help facilitate intelligent drug design in the future...

  5. In-situ neutron powder diffraction study of Ti3SiC2 synthesis

    International Nuclear Information System (INIS)

    Wu, E.; Kisi, E.H.; Kennedy, S.J.; Studer, A.J.

    2000-01-01

    Full text: The synthesis of Ti 3 SiC 2 by pressureless reactive sintering Ti/SiC/C mixtures under an Ar atmosphere has been studied by in-situ neutron diffraction. The intermediate phases TiC x and Ti 5 Si 5 C x (x ≤ 1) form first at ∼ 800 - 1400 deg C. These phases are consumed in the formation of Ti 3 SiC 2 , at ∼ 1500 deg C. An amount of TiC x remains in the sample after sintering, primarily as a surface layer. The studies appear to support a suggestion that these intermediate phases react to form Ti 3 SiC 2 through a diffusion controlled process. Prolonged step-wise heating under argon in some experiments results in decomposition of Ti 3 SiC 2 above ∼ 1400 deg C and significant disproportionation of the sample

  6. Calculations of single crystal elastic constants for yttria partially stabilised zirconia from powder diffraction data

    Science.gov (United States)

    Lunt, A. J. G.; Xie, M. Y.; Baimpas, N.; Zhang, S. Y.; Kabra, S.; Kelleher, J.; Neo, T. K.; Korsunsky, A. M.

    2014-08-01

    Yttria Stabilised Zirconia (YSZ) is a tough, phase-transforming ceramic that finds use in a wide range of commercial applications from dental prostheses to thermal barrier coatings. Micromechanical modelling of phase transformation can deliver reliable predictions in terms of the influence of temperature and stress. However, models must rely on the accurate knowledge of single crystal elastic stiffness constants. Some techniques for elastic stiffness determination are well-established. The most popular of these involve exploiting frequency shifts and phase velocities of acoustic waves. However, the application of these techniques to YSZ can be problematic due to the micro-twinning observed in larger crystals. Here, we propose an alternative approach based on selective elastic strain sampling (e.g., by diffraction) of grain ensembles sharing certain orientation, and the prediction of the same quantities by polycrystalline modelling, for example, the Reuss or Voigt average. The inverse problem arises consisting of adjusting the single crystal stiffness matrix to match the polycrystal predictions to observations. In the present model-matching study, we sought to determine the single crystal stiffness matrix of tetragonal YSZ using the results of time-of-flight neutron diffraction obtained from an in situ compression experiment and Finite Element modelling of the deformation of polycrystalline tetragonal YSZ. The best match between the model predictions and observations was obtained for the optimized stiffness values of C11 = 451, C33 = 302, C44 = 39, C66 = 82, C12 = 240, and C13 = 50 (units: GPa). Considering the significant amount of scatter in the published literature data, our result appears reasonably consistent.

  7. Report on neutron powder diffraction for the Australian Replacement Research Reactor

    International Nuclear Information System (INIS)

    Hunter, B.A.

    2000-01-01

    There is a clear need for two neutron powder diffractometers at the Australian Replacement Research Reactor when it starts operation in 2005. The high-intensity instrument should be capable of measuring a 10mg sample of moderate complexity, or perform single-shot time-resolved experiments with 1-second time slices, or perform stroboscopic measurements with time slices of order 50 microseconds. The high-resolution instrument should have a target resolution of Δd/d∼6x10 -4 , and be capable of collecting data at this resolution within 1-48 hours depending on sample size and crystal complexity. Key questions that need to be answered in the next 9 months include: (1) a detailed study of monochromator options, (2) analysing the detector options for the high-intensity machine and exploring ways in which the solid angle can be maximised for both instruments, (3) whether the instruments are better situated at the reactor face or on super mirror guides, (4) how to integrate the two instruments (physically, if they are only the same guide), and scientifically as regards detailed performance specifications. The user community clearly wants a wide range of sample-environment options, and these are listed in the report. Combinations of these options will be important

  8. Analysis of magnetic ordering in TbB12 by means of powder neutron diffraction

    International Nuclear Information System (INIS)

    Murasik, A.; Czopnik, A.; Shitsevalova, N.; Paderano, Y.; Keller, L.; Zolliker, M.

    2002-01-01

    The neutron diffraction study of the magnetically ordered TbB 12 reveals that its magnetic structure between (4.2-15) K is characterized by the coexistence of two magnetic phases which cannot be indexed within the reciprocal lattice point neither of the chemical cell nor with any simple multiple of it. As no higher order satellites were detected, the models considered were restricted to the sinusoidally modulated type. The incommensurate magnetic structure of TbB 12 has been satisfactory described by a single k = [1/2+τ, 1/2+τ, 1/2+τ] phase with some admixture of the phase describing a similar ordering but with somewhat different τ. At the temperature range (15-16) K a phase transition of the phase II to a paramagnetic state is observed. This effect is accompanied by a significant drop of magnetic moment amplitude of the phase I from 7.95 to 5.6 μ B with simultaneous differentiation of the sine-wave propagation along the [001] to [100] directions. In contrast to specific heat measurements no additional phase transition at ∼18 K was detected. (author)

  9. Taking a closer look for a broader view: combining powder diffraction with electron crystallography for a better understanding of modulated structures

    Czech Academy of Sciences Publication Activity Database

    Palatinus, Lukáš

    2015-01-01

    Roč. 71, Apr (2015), 125-126 ISSN 0108-7681 Institutional support: RVO:68378271 Keywords : transmission electron microscopy * powder diffraction * anion-deficient perovskites * modulated structures * diffuse Subject RIV: BM - Solid Matter Physics ; Magnetism Impact factor: 2.184, year: 2014

  10. Low-temperature phases in PbZr0.52Ti0.48O3 : A neutron powder diffraction study

    NARCIS (Netherlands)

    Cox, D.E.; Noheda, B.; Shirane, G.

    2005-01-01

    A neutron powder diffraction study has been carried out on PbZr0.52Ti0.48O3 in order to resolve an ongoing controversy about the nature of the low-temperature structure of this strongly piezoelectric and technologically important material. The results of a detailed and systematic Rietveld analysis

  11. Evaluation of laboratory powder X-ray micro-diffraction for applications in the fields of cultural heritage and forensic science

    Czech Academy of Sciences Publication Activity Database

    Švarcová, Silvie; Kočí, Eva; Bezdička, Petr; Hradil, David; Hradilová, J.

    2010-01-01

    Roč. 398, č. 2 (2010), s. 1061-1076 ISSN 1618-2642 R&D Projects: GA AV ČR KJB200320901 Institutional research plan: CEZ:AV0Z40320502 Keywords : powder X-ray micro-diffraction * quantitative phase analysis * forensic Subject RIV: CA - Inorganic Chemistry Impact factor: 3.841, year: 2010

  12. The determination of crystal structures of active pharmaceutical ingredients from X-ray powder diffraction data: a brief, practical introduction, with fexofenadine hydrochloride as example.

    Science.gov (United States)

    Brüning, Jürgen; Schmidt, Martin U

    2015-06-01

    This study describes the general method for the determination of the crystal structures of active pharmaceutical ingredients (API) from powder diffraction data and demonstrates its use to determine the hitherto unknown crystal structure of fexofenadine hydrochloride, a third-generation antihistamine drug. Fexofenadine hydrochloride was subjected to a series of crystallisation experiments using re-crystallisation from solvents, gas diffusion, layering with an antisolvent and gel crystallisation. Powder diffraction patterns of all samples were recorded and inspected for polymorphism and for crystallinity. All samples corresponded to the same polymorph. The crystal structure was determined from an X-ray powder diffraction pattern using a real-space method with subsequent Rietveld refinement. The structure exhibits a two-dimensional hydrogen bond network. Crystal structures of API can be determined from X-ray powder diffraction data with good reliability. Fexofenadine exhibits only one polymorphic form, which is stabilised in the crystal by strong hydrogen bonds of the type (+)N-H···Cl(-), O-H···Cl(-), and between COOH groups. © 2015 Royal Pharmaceutical Society.

  13. Void and Phase Evolution during the Processing of Bi-2212 Superconducting Wires monitored by combined fast Synchrotron Micro-tomography and X-Ray Diffraction

    CERN Document Server

    Scheuerlein, C; Scheel, M; Jiang, J; Kametani, F; Malagoli, A; Hellstrom, E E; Larbalestier, D C

    2011-01-01

    Recent study of the current-limiting mechanisms in Bi-2212 round wires has suggested that agglomeration of the residual Bi-2212 powder porosity into bubbles of filament-diameter size occurs on melting the Bi-2212 filaments. These pores introduce a major obstacle to current flow, which greatly reduces the critical current density (Jc). Here we present an in situ non-destructive tomographic and diffraction study of the changes occurring during the heat treatment of wires and starting powder, as well as a room temperature study of ex situ processed wires. The in situ through-process study shows that the agglomeration of residual porosity is more complex than previously seen. Filament changes start with coalescence of the quasi-uniform and finely divided powder porosity into lens-shaped defects at about 850 0C when the Bi-2201 impurity phase decomposes before the Bi-2212 starts to melt. These lens-shaped voids grow to bubbles of a filament diameter on melting of the Bi-2212 and continue to lengthen and then to ag...

  14. Crystal Engineering on Industrial Diaryl Pigments Using Lattice Energy Minimizations and X-ray Powder Diffraction

    International Nuclear Information System (INIS)

    Schmidt, M.; Dinnebier, R.; Kalkhof, H.

    2007-01-01

    Diaryl azo pigments play an important role as yellow pigments for printing inks, with an annual pigment production of more than 50,000 t. The crystal structures of Pigment Yellow 12 (PY12), Pigment Yellow 13 (PY13), Pigment Yellow 14 (PY14), and Pigment Yellow 83 (PY83) were determined from X-ray powder data using lattice energy minimizations and subsequent Rietveld refinements. Details of the lattice energy minimization procedure and of the development of a torsion potential for the biphenyl fragment are given. The Rietveld refinements were carried out using rigid bodies, or constraints. It was also possible to refine all atomic positions individually without any constraint or restraint, even for PY12 having 44 independent non-hydrogen atoms per asymmetric unit. For PY14 (23 independent non-hydrogen atoms), additionally all atomic isotropic temperature factors could be refined individually. PY12 crystallized in a herringbone arrangement with twisted biaryl fragments. PY13 and PY14 formed a layer structure of planar molecules. PY83 showed a herringbone structure with planar molecules. According to quantum mechanical calculations, the twisting of the biaryl fragment results in a lower color strength of the pigments, whereas changes in the substitution pattern have almost no influence on the color strength of a single molecule. Hence, the experimentally observed lower color strength of PY12 in comparison with that of PY13 and PY83 can be explained as a pure packing effect. Further lattice energy calculations explained that the four investigated pigments crystallize in three different structures because these structures are the energetically most favorable ones for each compound. For example, for PY13, PY14, or PY83, a PY12-analogous crystal structure would lead to considerably poorer lattice energies and lower densities. In contrast, lattice energy calculations revealed that PY12 could adopt a PY13-type structure with only slightly poorer energy. This structure was

  15. Stress distribution during cold compression of a quartz aggregate using synchrotron X-ray diffraction: Observed yielding, damage, and grain crushing: STRESS DISTRIBUTION OF QUARTZ AGGREGATE

    Energy Technology Data Exchange (ETDEWEB)

    Cheung, C. S. N. [Mineral Physics Institute, Stony Brook University, Stony Brook New York USA; Geological Engineering, University of Wisconsin-Madison, Madison Wisconsin USA; Weidner, D. J. [Mineral Physics Institute, Stony Brook University, Stony Brook New York USA; Li, L. [Mineral Physics Institute, Stony Brook University, Stony Brook New York USA; Meredith, P. G. [Rock and Ice Physics Laboratory, Department of Earth Sciences, University College London, London UK; Chen, H. [Mineral Physics Institute, Stony Brook University, Stony Brook New York USA; Whitaker, M. L. [Mineral Physics Institute, Stony Brook University, Stony Brook New York USA; Chen, X. [Chemistry Department, Stony Brook University, Stony Brook New York USA

    2017-04-01

    We report new experimental results that quantify the stress distribution within a quartz aggregate during pore collapse and grain crushing. The samples were probed with synchrotron X-ray diffraction as they were compressed in a multianvil deformation apparatus at room temperature from low pressure (tens of megapascal) to pressures of a few gigapascal. In such a material, stress is likely to concentrate at grain-to-grain contacts and vanish where grains are bounded by open porosity. Therefore, internal stress is likely to vary significantly from point to point in such an aggregate, and hence, it is important to understand both the heterogeneity and anisotropy of such variation with respect to the externally applied stress. In our quartz aggregate (grain size of ~4 μm), the measured diffraction peaks broaden asymmetrically at low pressure (tens of megapascal), suggesting that open pores are still a dominant characteristic of grain boundaries. In contrast, a reference sample of novaculite (a highly dense quartz polycrystal, grain size of ~6–9 μm) showed virtually no peak broadening with increasing pressure. In the quartz aggregate, we observed significant deviation in the pressure-volume curves in the range of P = 400–600 MPa. We suggest that this marks the onset of grain crushing (generally denoted as P* in the rock mechanic literature), which is commonly reported to occur in sandstones at pressures of this order, in general agreement with a Hertzian analysis of fracturing at grain contacts.

  16. A synchrotron X-ray diffraction deconvolution method for the measurement of residual stress in thermal barrier coatings as a function of depth.

    Science.gov (United States)

    Li, C; Jacques, S D M; Chen, Y; Daisenberger, D; Xiao, P; Markocsan, N; Nylen, P; Cernik, R J

    2016-12-01

    The average residual stress distribution as a function of depth in an air plasma-sprayed yttria stabilized zirconia top coat used in thermal barrier coating (TBC) systems was measured using synchrotron radiation X-ray diffraction in reflection geometry on station I15 at Diamond Light Source, UK, employing a series of incidence angles. The stress values were calculated from data deconvoluted from diffraction patterns collected at increasing depths. The stress was found to be compressive through the thickness of the TBC and a fluctuation in the trend of the stress profile was indicated in some samples. Typically this fluctuation was observed to increase from the surface to the middle of the coating, decrease a little and then increase again towards the interface. The stress at the interface region was observed to be around 300 MPa, which agrees well with the reported values. The trend of the observed residual stress was found to be related to the crack distribution in the samples, in particular a large crack propagating from the middle of the coating. The method shows promise for the development of a nondestructive test for as-manufactured samples.

  17. Characterisation of corrosion deposits induced by carbon dioxide on mild steel using grazing incidence x-ray and synchrotron radiation diffraction

    International Nuclear Information System (INIS)

    Sembiring, S.; O'Connor, B; Li, D.; Buckley, C.; Van Riessen, A.; De Marco, R.

    1999-01-01

    Full text: Grazing incidence diffraction, using x-rays (GIXRD) and synchrotron radiation (GISRD), is being applied for near-surface characterisation of corrosion deposits formed on the internal surfaces of mild steel pipelines which are used to deliver natural gas from offshore deposits in Western Australia. These techniques are being employed to construct phase composition depth-profiles of corrosion product phases. The GIXRD data are being measured with CuKα radiation using a Siemens D5000 x-ray diffractometer, fitted with a primary beam slit system for incidence angle control and also with a diffracted beam monochromator; and the GISRD data have been acquired with the BIGDIFF instrument on the ANBF beamline in Tsukuba, Japan. The mild steel test samples are prepared with a laboratory reactor in which the corrosion conditions are simulated in a controlled manner. Results obtained to date have shown that two phases are readily observed in addition to the a-Fe phase from the mild steel substrate: (1) FeCO 3 (siderite) induced by CO 2 dissolved in the water flowing through the pipeline, and (2) CaCO 3 (calcite) deposited on the mild steel surface by reaction between the CO 2 and calcium ions which are also present in the water flowing through the pipeline. Supporting measurements from SEM imaging and associated EDS analysis will also be presented

  18. In Situ Synchrotron X-Ray Diffraction Characterization of the Synthesis of Graphene Oxide and Reduced Graphene Oxide

    DEFF Research Database (Denmark)

    Storm, Mie Møller; Johnsen, Rune E.; Norby, Poul

    2015-01-01

    the third stage. The in situ XRD results of the thermal reduction of GO to rGO showed a dependence on the temperature ramping and addition of diamond powder. Syntheses were measured at 1, 5, 10, 20 and 50 °/min temperature ramps. The syntheses were performed in a capillary with GO being heated by a hot air...... during the thermal reduction of GO. The stages observed for both syntheses illuminate how important it is to consider the experimental parameters dependent on the application; they might even have to be optimized separately. As the future use of GO and rGO is expanding and the commercialization...

  19. Synchrotron Bragg diffraction imaging characterization of synthetic diamond crystals for optical and electronic power device applications1 1

    Science.gov (United States)

    Tran Thi, Thu Nhi; Morse, J.; Caliste, D.; Fernandez, B.; Eon, D.; Härtwig, J.; Mer-Calfati, C.; Tranchant, N.; Arnault, J. C.; Lafford, T. A.; Baruchel, J.

    2017-01-01

    Bragg diffraction imaging enables the quality of synthetic single-crystal diamond substrates and their overgrown, mostly doped, diamond layers to be characterized. This is very important for improving diamond-based devices produced for X-ray optics and power electronics applications. The usual first step for this characterization is white-beam X-ray diffraction topography, which is a simple and fast method to identify the extended defects (dislocations, growth sectors, boundaries, stacking faults, overall curvature etc.) within the crystal. This allows easy and quick comparison of the crystal quality of diamond plates available from various commercial suppliers. When needed, rocking curve imaging (RCI) is also employed, which is the quantitative counterpart of monochromatic Bragg diffraction imaging. RCI enables the local determination of both the effective misorientation, which results from lattice parameter variation and the local lattice tilt, and the local Bragg position. Maps derived from these parameters are used to measure the magnitude of the distortions associated with polishing damage and the depth of this damage within the volume of the crystal. For overgrown layers, these maps also reveal the distortion induced by the incorporation of impurities such as boron, or the lattice parameter variations associated with the presence of growth-incorporated nitrogen. These techniques are described, and their capabilities for studying the quality of diamond substrates and overgrown layers, and the surface damage caused by mechanical polishing, are illustrated by examples. PMID:28381981

  20. Structural and microstructural changes during anion exchange of CoAl layered double hydroxides. An in situ X-ray powder diffraction study

    International Nuclear Information System (INIS)

    Johnsen, Rune E.; Krumeich, Frank; Norby, Poul

    2010-01-01

    Anion-exchange processes in cobalt-aluminium layered double hydroxides (LDHs) were studied by in situ synchrotron X-ray powder diffraction (XRPD). The processes investigated were CoAl-CO 3 →CoAl-Cl →CoAl-CO 3 , CoAl-Cl→CoAl-NO 3 and CoAl-CO 3 →CoAl-SO 4 . The XRPD data show that the CoAl-CO 3 →CoAl-Cl process is a two-phase transformation, where the amount of the CoAl-CO 3 phase decreases exponentially while that of the CoAl-Cl phase increases exponentially. Energy-dispersive X-ray spectroscopy (EDXS) studies of a partially chloride-exchanged CoAl-CO 3 LDH sample along with in situ XRPD data suggested that the individual particles in the CoAl-CO 3 sample are generally anion-exchanged with chloride one at a time. In contrast with the CoAl-CO 3 →CoAl-Cl transformation, the XRPD data show that the reverse CoAl-Cl→CoAl-CO 3 process is a one-phase transformation. Rietveld refinements indicate that the occupancy factors of the carbon and oxygen sites of the carbonate group increase, while that of the chloride site decreases. In the CoAl-Cl→CoAl-NO 3 anion-exchange reaction, the XRPD patterns reveal the existence of two intermediate phases in addition to the initial CoAl-Cl and final CoAl-NO 3 phases. The in situ data indicate that one of these intermediates is a mixed nitrate- and chloride-based LDH phase, where the disorder decreases as the nitrate content increases. The XRPD data of the partial CoAl-CO 3 →CoAl-SO 4 anion-exchange reaction show that the process is a two-phase transformation involving a sulfate-containing LDH with a 1H polytype structure. (orig.)

  1. Application of Powder Diffraction Methods to the Analysis of the Atomic Structure of Nanocrystals: The Concept of the Apparent Lattice Parameter (ALP)

    Science.gov (United States)

    Palosz, B.; Grzanka, E.; Gierlotka, S.; Stelmakh, S.; Pielaszek, R.; Bismayer, U.; Weber, H.-P.; Palosz, W.; Curreri, Peter A. (Technical Monitor)

    2002-01-01

    The applicability of standard methods of elaboration of powder diffraction data for determination of the structure of nano-size crystallites is analysed. Based on our theoretical calculations of powder diffraction data we show, that the assumption of the infinite crystal lattice for nanocrystals smaller than 20 nm in size is not justified. Application of conventional tools developed for elaboration of powder diffraction data, like the Rietveld method, may lead to erroneous interpretation of the experimental results. An alternate evaluation of diffraction data of nanoparticles, based on the so-called 'apparent lattice parameter' (alp) is introduced. We assume a model of nanocrystal having a grain core with well-defined crystal structure, surrounded by a surface shell with the atomic structure similar to that of the core but being under a strain (compressive or tensile). The two structural components, the core and the shell, form essentially a composite crystal with interfering, inseparable diffraction properties. Because the structure of such a nanocrystal is not uniform, it defies the basic definitions of an unambiguous crystallographic phase. Consequently, a set of lattice parameters used for characterization of simple crystal phases is insufficient for a proper description of the complex structure of nanocrystals. We developed a method of evaluation of powder diffraction data of nanocrystals, which refers to a core-shell model and is based on the 'apparent lattice parameter' methodology. For a given diffraction pattem, the alp values are calculated for every individual Bragg reflection. For nanocrystals the alp values depend on the diffraction vector Q. By modeling different a0tomic structures of nanocrystals and calculating theoretically corresponding diffraction patterns using the Debye functions we showed, that alp-Q plots show characteristic shapes which can be used for evaluation of the atomic structure of the core-shell system. We show, that using a simple

  2. PHASE ANALYSIS OF NITI WIRE BASED ON SYNCHROTRON 2D X-RAY DIFFRACTION PATTERN IN MATLAB

    Directory of Open Access Journals (Sweden)

    Martin Dudr

    2017-07-01

    Full Text Available This paper deals with simplified phase analysis of 2D diffraction patterns obtained using microfocused X-ray at various places of superelastic NiTi wire under combined load. For this purpose, MATLAB routines and functions were created, which carry out integration of the patterns in various sectors of Debye ring, fitting of the patterns by a mixture of austenite and martensite (having neglected the R-phase and successive evaluation of the quantitative phase content. The most crucial simplificating assumptions were: the neglection of the R-phase and the assumption of a fibre texture or b no texture.

  3. Instrumentation of x-ray diffraction and materials research on the National Synchrotron Light Source. Final report

    International Nuclear Information System (INIS)

    Liedl, G.L.

    1984-11-01

    MATRIX was organized in 1980 to formulate a research team to design and construct a beam line at NSLS for x-ray diffraction studies of materials. A versatile system was designed to allow a full range of experimental capabilities for wide angle x-ray scattering experiments including surface diffraction studies. The design and construction of the system has been completed. Testing of parts of the system was completed at CHESS and with x-ray sources or other equipment at member institutions. Installation of the beam line at NSLS is in progress and will proceed in parallel with the commissioning of the x-ray ring at NSLS. Full operation of the beam line is expected to be ready by December 1, 1984 being limited only by the source power of NSLS at that time. Useful experiments could be started if the power is at least 2 GeV and 100ma. The MATRIX beam line was one of the first x-ray beam lines to see light in the beam line in early spring of 1984. In July of 1984, the MATRIX beam line as the first port at NSLS to have a monochromatic beam and to scan part of the spectrum from the source. As part of this contract, six publications have resulted from the various projects. Three publications are concerned directly with the beam line and/or its operation while the other three publications are the result of research associated with the project

  4. X-ray Powder Diffraction in Conservation Science: Towards Routine Crystal Structure Determination of Corrosion Products on Heritage Art Objects.

    Science.gov (United States)

    Dinnebier, Robert E; Fischer, Andrea; Eggert, Gerhard; Runčevski, Tomče; Wahlberg, Nanna

    2016-06-08

    The crystal structure determination and refinement process of corrosion products on historic art objects using laboratory high-resolution X-ray powder diffraction (XRPD) is presented in detail via two case studies. The first material under investigation was sodium copper formate hydroxide oxide hydrate, Cu4Na4O(HCOO)8(OH)2∙4H2O (sample 1) which forms on soda glass/copper alloy composite historic objects (e.g., enamels) in museum collections, exposed to formaldehyde and formic acid emitted from wooden storage cabinets, adhesives, etc. This degradation phenomenon has recently been characterized as "glass induced metal corrosion". For the second case study, thecotrichite, Ca3(CH3COO)3Cl(NO3)2∙6H2O (sample 2), was chosen, which is an efflorescent salt forming needlelike crystallites on tiles and limestone objects which are stored in wooden cabinets and display cases. In this case, the wood acts as source for acetic acid which reacts with soluble chloride and nitrate salts from the artifact or its environment. The knowledge of the geometrical structure helps conservation science to better understand production and decay reactions and to allow for full quantitative analysis in the frequent case of mixtures.

  5. Effect of powder sample granularity on fluorescent intensity and on thermal parameters in x-ray diffraction Rietveld analysis

    International Nuclear Information System (INIS)

    Sparks, C.J.; Specht, E.D.; Ice, G.E.; Kumar, R.; Zschack, P.; Shiraishi, T.; Hisatsune, K.

    1991-01-01

    The effect of sample granularity on diffracted x-ray intensity was evaluated by measuring the 2θ dependence of x-ray fluorescence from various samples. Measurements were made in the symmetric geometry on samples ranging from single crystals to highly absorbing coarse powders. A characteristic shape for the absorption correction was observed. A demonstration of the sensitivity of Rietveld refined site occupation parameters is made on CuAu and Cu 50 Au 44 Ni 6 alloys refined with and without granularity corrections. These alloys provide a good example of the effect of granularity due to their large linear x-ray absorption coefficients. Sample granularity and refined thermal parameters obtained from the Rietveld analysis were found to be correlated. Without a granularity correction, the refined thermal parameters are too low and can actually become negative in an attempt to compensate for granularity. A general shape for granularity correction can be included in refinement procedures. If no granularity correction is included, data should be restricted to above 30 degrees 2θ, and thermal parameters should be ignored unless extreme precautions are taken to produce >5 μm particles and high packing densities

  6. Ab initio determination of the novel perovskite-related structure of La7Mo7O30 from powder diffraction

    International Nuclear Information System (INIS)

    Goutenoire, F.; Retoux, R.; Lacorre, P.

    1999-01-01

    A new mixed valence molybdate, La 7 Mo 7 O 30 , first prepared by high energy ball milling, has been successfully synthesized by controlled hydrogen reduction of La 2 Mo 2 O 9 . Its original crystal structure was determined from X-ray and neutron powder diffraction (space group R 3 ; a = b = 17.0051(2) angstrom, c = 6.8607(1) angstrom; Z = 3; reliability factors: R p = 0.081, R wp = 0.091, χ 2 = 3.1, R Bragg = 0.049, R F = 0.033). It consists in the hexagonal stacking of individual cylinders of perovskite-type arrangement. These cylinders are built up from perovskite cages sharing corners in trans-position along their diagonal axis. Two different mixed-valence molybdenum sites coexist, with more (Mo +5.75 ) or less (Mo +4.5 ) distorted octahedral environments. Lanthanum atoms are located within the perovskite cages and around them, very close to their regular positions in the perovskite structure. Lanthanum and molybdenum atoms thus form two rows of almost perfect cubes, shifted from each other by c/2. An electron microscopy study revealed the defect-free cationic and octahedral arrangements in the (a,b) plane

  7. The crystal structure of lueshite at 298 K resolved by high-resolution time-of-flight neutron powder diffraction

    Science.gov (United States)

    Mitchell, Roger H.; Kennedy, Brendan J.; Knight, Kevin S.

    2018-01-01

    Refinement of time-of-flight high-resolution neutron powder diffraction data for lueshite (Na, Ca)(Nb, Ta, Ti)O3, the natural analogue of synthetic NaNbO3, demonstrates that lueshite at room temperature (298 K) adopts an orthorhombic structure with a 2 a p × 2 a p × 4 a p superlattice described by space group Pmmn [#59: a = 7.8032(4) Å; b = 7.8193(4) Å; c = 15.6156(9) Å]. This structure is analogous to that of phase S of synthetic NaNbO3 observed at 753-783 K (480-510 °C). In common with synthetic NaNbO3, lueshite exhibits a series of phase transitions with decreasing temperature from a cubic (Pm\\bar{3}m) aristotype through tetragonal ( P4/ mbm) and orthorhombic ( Cmcm) structures. However, the further sequence of phase transitions differs in that for lueshite the series terminates with the room temperature S ( Pmmn) phase, and the R ( Pmmn or Pnma) and P ( Pbcm) phases of NaNbO3 are not observed. The appearance of the S phase in lueshite at a lower temperature, relative to that of NaNbO3, is attributable to the effects of solid solution of Ti, Ta and Ca in lueshite.

  8. Using Neutron Diffraction to Investigate Texture Evolution During Consolidation of Deuterated Triaminotrinitrobenzene (d-TATB Explosive Powder

    Directory of Open Access Journals (Sweden)

    Darby J. Luscher

    2017-05-01

    Full Text Available Triaminotrinitrobenzene (TATB is a highly anisotropic molecular crystal used in several plastic-bonded explosive (PBX formulations. A complete understanding of the orientation distribution of TATB particles throughout a PBX charge is required to understand spatially variable, anisotropic macroscale properties of the charge. Although texture of these materials can be measured after they have been subjected to mechanical or thermal loads, measuring texture evolution in situ is important in order to identify mechanisms of crystal deformation and reorientation used to better inform thermomechanical models. Neutron diffraction measurements were used to estimate crystallographic reorientation while deuterated TATB (d-TATB powder was consolidated into a cylindrical pellet via a uniaxial die-pressing operation at room temperature. Both the final texture of the pressed pellet and the in situ evolution of texture during pressing were measured, showing that the d-TATB grains reorient such that (001 poles become preferentially aligned with the pressing direction. A compaction model is used to predict the evolution of texture in the pellet during the pressing process, finding that the original model overpredicted the texture strength compared to these measurements. The theory was extended to account for initial particle shape and pore space, bringing the results into good agreement with the data.

  9. Operation manual for EDXRDDA - a software package for Bragg peak analysis of energy dispersive powder X-ray diffraction data

    International Nuclear Information System (INIS)

    Jayaswal, Balhans; Vijaykumar, V.; Momin, S.N.; Sikka, S.K.

    1992-01-01

    EDXRDDA is a software package for analysis of raw data for energy dispersive x-ray diffraction from powder samples. It resolves the spectra into individual peaks by a constrained non-linear least squares method (Hughes and Sexton, 1988). The profile function adopted is the Gaussian/Lorentzian product with the mixing ratio refinable in the program. The program is implemented on an IBM PC and is highly interactive with extensive plotting facilities. This report is a user's guide for running the program. In the first step after inputting the spectra, the full spectra is plotted on the screen. The user then chooses a portion of this for peak resolution. The initial guess for the peak intensity, peak position are input with the help of a cursor or a mouse. Upto twenty peaks can be fitted at a time in an interval of 500 channels. For overlapping peaks, various constraints can be applied. Bragg peaks and fluorescence peaks with different half widths can be handled simultaneously. The program on execution produces a look up table which contains the refined values of the peak position, half width, peak intensity, integrated intensity, and their error estimates of each peak. The program is very general and can also be used for curve fitting of data from many other experiments. (author). 2 refs., 7 figs., 2 appendices

  10. Structures of the ZrO2 polymorphs at room temperature by high-resolution neutron powder diffraction

    International Nuclear Information System (INIS)

    Howard, C.J.; Hill, R.J.; Reichert, B.E.

    1988-01-01

    The crystal structures of monoclinic ZrO 2 [P2 1 /c, a=5.1505(1), b=5.2116(1), c=5.3173(1) A, β=99.230(1) 0 , V=140.88(1) A 3 , Z=4, R wp =0.047], tetragonal Zr 0.935 Y 0.065 O 1.968 [P4 2 /nmc, a=3.6055(1), c=5.1797(2) A, V=67.33(1) A 3 , Z=2, R wp =0.090] and cubic Zr 0.875 Mg 0.125 O 1.875 [Fm3m, a=5.0858(1) A, V=131.55(1) A 3 , Z=4, R wp =0.083] have been refined by Rietveld analysis of 1.377 A neutron powder diffraction data collected at 295 K. In both tetragonal and cubic ZrO 2 , the stabilizer atoms randomly occupy the Zr site and charge balance is achieved by an appropriate number of vacancies on the O site. In cubic ZrO 2 , the anions are displaced from their ideal fluorite positions by 0.025a in the [111] direction and there is evidence for the presence of either a small quantity of a tetragonal impurity phase, or a slight tetragonal distortion. (orig.)

  11. High-energy synchrotron X-ray diffraction measurements of simple bending of pseudoelastic NiTi shape memory alloy wires

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Baozhuo; Young, Marcus L.

    2016-05-23

    Many technological applications of austenitic shape memory alloys (SMAs) involve cyclical mechanical loading and unloading in order to take advantage of pseudoelasticity. In this paper, we investigated the effect of mechanical bending of pseudoelastic NiTi SMA wires using high-energy synchrotron radiation X-ray diffraction (SR-XRD). Differential scanning calorimetry was performed to identify the phase transformation temperatures. Scanning electron microscopy images show that micro-cracks in compressive regions of the wire propagate with increasing bend angle, while tensile regions tend not to exhibit crack propagation. SR-XRD patterns were analyzed to study the phase transformation and investigate micromechanical properties. By observing the various diffraction peaks such as the austenite (200) and the martensite (${\\bar 1}12$), (${\\bar 1}03$), (${\\bar 1}11$), and (101) planes, intensities and residual strain values exhibit strong anisotropy, depending upon whether the sample is in compression or tension during bending.

  12. Interfacial reaction pathways and kinetics during annealing of 111-textured Al/TiN bilayers: A synchrotron x-ray diffraction and transmission electron microscopy study

    International Nuclear Information System (INIS)

    Chun, J.-S.; Desjardins, P.; Lavoie, C.; Petrov, I.; Cabral, C. Jr.; Greene, J. E.

    2001-01-01

    Growth of TiN layers in most diffusion-barrier applications is limited to deposition temperatures T s s =450 deg. C on SiO 2 by ultrahigh vacuum reactive magnetron sputter deposition in pure N 2 . Al overlayers, 160 nm thick with inherited 111 preferred orientation, were then deposited at T s =100 deg. C without breaking vacuum. The as-deposited TiN layer is underdense due to the low deposition temperature (T s /T m ≅0.23 in which T m is the melting point) resulting in kinetically limited adatom mobilities leading to atomic shadowing which, in turn, results in a columnar microstructure with both inter- and intracolumnar voids. The Al overlayer is fully dense. Synchrotron x-ray diffraction was used to follow interfacial reaction kinetics during postdeposition annealing of the 111-textured Al/TiN bilayers as a function of time (t a =12-1200 s) and temperature (T a =440-550 deg. C). Changes in bilayer microstructure and microchemistry were investigated using transmission electron microscopy (TEM) and scanning TEM to obtain compositional maps of plan-view and cross-sectional specimens. Interfacial reaction during annealing is initiated at the Al/TiN interface. Al diffuses rapidly into TiN voids during anneals at temperatures ∼ 3 Ti at the interface. Al 3 Ti exhibits a relatively planar growth front extending toward the Al free surface. Analyses of time-dependent x-ray diffraction peak intensities during isothermal annealing as a function of temperature show that Al 3 Ti growth kinetics are, for the entire temperature range investigated, diffusion limited with an activation energy of 1.5±0.2 eV

  13. Study of the phase transformations and equation of state of magnesium by synchrotron x-ray diffraction

    CERN Document Server

    Errandonea, D; Häusermann, D; Uchida, T

    2003-01-01

    We studied the phase behaviour and the P - V - T equation of state of Mg by in situ energy-dispersive x-ray diffraction in a multi-anvil apparatus in the pressure-temperature range up to 18.6 GPa and 1527 K. At high temperatures, an hcp to dhcp transition was found above 9.6 GPa, which differs from the hcp to bcc transformation predicted by theoretical calculations. At room temperature, the hcp phase remains stable within the pressure range of this study with an axial ratio, c/a, close to the ideal. The melting of Mg was determined at 2.2, 10 and 12 GPa; the detected melting temperatures are in good agreement with previous diamond anvil cell results. The P - V - T equation of state determined based on the data of this study gives B sub 0 = (36.8 +- 3) GPa, B sub 0 ' = 4.3 +- 0.4, alpha sub 0 = 25 x 10 sup - sup 6 K sup - sup 1 , partial deriv alpha/partial deriv T = (2.3 +- 0.2) x 10 sup - sup 7 K sup - sup 2 and partial deriv B sub 0 sub , sub T /partial deriv T = (-2.08 +- 0.09) x 10 sup - sup 2 GPa K sup -...

  14. High pressure neutron powder diffraction study of Fe1-xCrx with and without hydrogen exposure

    Energy Technology Data Exchange (ETDEWEB)

    Rivin, Oleg [Nuclear Research Centre, Negev (Israel); Broide, Amir [Ben Gurion Univ., Beersheba (Israel); Maskova, Sylvie [Charles Univ., Prague (Czech Republic); Lucas, Matthew [Air Force Research Lab. (AFRL), Wright-Patterson AFB, OH (United States); Hen, Amir [Ben Gurion Univ., Beersheba (Israel); Orion, Itzhak [Ben Gurion Univ., Beersheba (Israel); Salhov, Shai [Nuclear Research Centre, Negev(Israel); Shandalov, Michael [Nuclear Research Centre, Negev(Israel); Moreira Dos Santos, Antonio F. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Molaison, Jamie J. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Chen, Zhiqiang [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Halevy, Itzhak [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States)

    2014-12-23

    The crystal structure of Fe1-xCrx(x = 0, 0.2 and 0.4) materials, with and without exposure to Hydrogen, is investigated using neutron powder diffraction under the applied external high-pressure. Above a certain applied pressure, PC, a structural phase transition, from cubic to hexagonal symmetry, is observed, in agreement with previous x-ray diffraction results. The PC values exhibit an increase with x increase. The possibility for an evolution of a magnetic structure with pressure, x and Hydrogen exposure, is examined. Finally, a broadening of the angular profile of the (200) reflection (cubic phase) is identified and reported.

  15. In situ synchrotron X-ray diffraction of ferroelastic La0.8Ca0.2CoO3 ceramics during uniaxial compression

    International Nuclear Information System (INIS)

    Vullum, Per Erik; Mastin, Johann; Wright, Jonathan; Einarsrud, Mari-Ann; Holmestad, Randi; Grande, Tor

    2006-01-01

    Uniaxial compression of rhombohedral La 0.8 Ca 0.2 CoO 3 ceramics has been studied in situ using synchrotron X-ray diffraction. The intensities of Bragg reflections parallel and perpendicular to the stress field were simultaneously detected as a function of the stress. Reorientation of ferroelastic domains due to the uniaxial stress was demonstrated. With increasing stress the volume fraction of domains with the hexagonal c-axis parallel to the stress axis increased at the expense of domains with the c-axis perpendicular to the stress axis. The strain in the polycrystalline materials evolved unevenly with increasing stress due to crystallographic anisotropy. In energetically favourable domains with the c-axis parallel to the stress axis, the rhombohedral distortion from cubic symmetry increased, while the crystal structure became closer to cubic in domains with the c-axis perpendicular to the stress. Successive compression/decompression cycles to higher maximum stress resulted in a higher volume fraction of reoriented domains both at maximum stress and after decompression

  16. In situ electrochemical impedance spectroscopy/synchrotron radiation grazing incidence X-ray diffraction-A powerful new technique for the characterization of electrochemical surfaces and interfaces

    International Nuclear Information System (INIS)

    De Marco, Roland; Jiang, Z.-T.; Martizano, Jay; Lowe, Alex; Pejcic, Bobby; Riessen, Arie van

    2006-01-01

    A marriage of electrochemical impedance spectroscopy (EIS) and in situ synchrotron radiation grazing incidence X-ray diffraction (SR-GIXRD) has provided a powerful new technique for the elucidation of the mechanistic chemistry of electrochemical systems. In this study, EIS/SR-GIXRD has been used to investigate the influence of metal ion buffer calibration ligands, along with natural organic ligands in seawater, on the behaviour of the iron chalcogenide glass ion-selective electrode (ISE). The SR-GIXRD data demonstrated that citrate - a previously reported poor iron calibration ligand for the analysis of seawater - induced an instantaneous and total dissolution of crystalline GeSe and Sb 2 Se 3 in the modified surface layer (MSL) of the ISE, while natural organic ligands in seawater and a mixture of ligands in a mimetic seawater ligand system protected the MSL's crystalline inclusions of GeSe and Sb 2 Se 3 from oxidative attack. Expectedly, the EIS data showed that citrate induced a loss in the medium frequency time constant for the MSL of the ISE, while seawater's natural organic ligands and the mimetic ligand system preserved the medium frequency EIS response characteristics of the ISE's MSL. The new EIS/SR-GIXRD technique has provided insights into the suitability of iron calibration ligands for the analysis of iron in seawater

  17. Experimental Charge Density in an Oxidized Trinuclear Iron Complex using 15 K Synchrotron and 100 K Conventional Single-Crystal X-ray Diffraction

    International Nuclear Information System (INIS)

    Overgaard, J.; Larsen, F.; Timco, G.; Iversen, B.

    2009-01-01

    The experimental electron density distribution in a crystal consisting of the simplest conceivable trinuclear carboxylate-bridged iron-μ3-oxo dianion with two α-picolinium cations has been determined using both synchrotron (15 K) and conventional (100 K) X-ray diffraction data. The constituent trinuclear oxo-centered molecule consists of six 2-bridging formate groups between the iron pairs, while the axial ligand for all iron atoms is another formate group. The compound {(Fe3O(HCOO)6(HCOO)3)2-·H2O·2(α-CH3NC5H5)+}, ( 1) crystallizes in the monoclinic space group P21/m with charge assisted hydrogen bonds linking the α-picolinium cations to the trinuclear groups. The chemical bonding in the weakly asymmetric Fe3O-core of 1 has been examined through the use of the quantum theory of atoms in molecules, and in combination with experimental d-orbital populations, a significant electron sharing is observed between the Fe atoms and the central oxygen. The central oxygen exhibits clear sp2 hybridization, and the iron atoms have valence shell charge concentrations in all metal-ligand bond directions. The relative bond strengths are evaluated based upon the charge density distribution and found to be in accordance with the geometrical results. Integrated group charges follow expectations from formal chemical valences.

  18. Trace elements in natural azurite pigments found in illuminated manuscript leaves investigated by synchrotron x-ray fluorescence and diffraction mapping

    Energy Technology Data Exchange (ETDEWEB)

    Smieska, Louisa M.; Woll, Arthur R. [Cornell High Energy Synchrotron Source, Wilson Laboratory, Ithaca, NY (United States); Mullett, Ruth [Cornell University, Medieval Studies Program, Ithaca, NY (United States); Ferri, Laurent [Cornell University, Cornell Library Rare and Manuscript Collections, Ithaca, NY (United States)

    2017-07-15

    We present trace-element and composition analysis of azurite pigments in six illuminated manuscript leaves, dating from the thirteenth to sixteenth century, using synchrotron-based, large-area x-ray fluorescence (SR-XRF) and diffraction (SR-XRD) mapping. SR-XRF mapping reveals several trace elements correlated with azurite, including arsenic, zirconium, antimony, barium, and bismuth, that appear in multiple manuscripts but were not always detected by point XRF. Within some manuscript leaves, variations in the concentration of trace elements associated with azurite coincide with distinct regions of the illuminations, suggesting systematic differences in azurite preparation or purification. Variations of the trace element concentrations in azurite are greater among different manuscript leaves than the variations within each individual leaf, suggesting the possibility that such impurities reflect distinct mineralogical/geologic sources. SR-XRD maps collected simultaneously with the SR-XRF maps confirm the identification of azurite regions and are consistent with impurities found in natural mineral sources of azurite. In general, our results suggest the feasibility of using azurite trace element analysis for provenance studies of illuminated manuscript fragments, and demonstrate the value of XRF mapping in non-destructive determination of trace element concentrations within a single pigment. (orig.)

  19. An in situ synchrotron X-ray diffraction study of precipitation kinetics in a severely deformed Cu–Ni–Si alloy

    Energy Technology Data Exchange (ETDEWEB)

    Azzeddine, H.; Mehdi, B. [Faculty of Physics, USTHB, BP 32 El-Alia, Dar El Beida, Algiers (Algeria); Hennet, L. [Conditions Extrêmes et Matériaux: Haute Température et Irradiation, CNRS-CEMHTI, 1D Ave de la Recherche Scientifique, 45071 Orléans Cedex 2 (France); Thiaudière, D. [Synchrotron SOLEIL, L' Orme des Merisiers, Saint-Aubin, 91192 Gif-sur-Yvette Cedex (France); Alili, B. [Faculty of Physics, USTHB, BP 32 El-Alia, Dar El Beida, Algiers (Algeria); Kawasaki, M., E-mail: megumi@hanyang.ac.kr [Division of Materials Science and Engineering, Hanyang University, 17 Haengdang-dong, Seongdong-gu, Seoul 133-791 (Korea, Republic of); Departments of Aerospace and Mechanical Engineering and Materials Science, University of Southern California, Los Angeles, CA 90089-1453 (United States); Bradai, D. [Faculty of Physics, USTHB, BP 32 El-Alia, Dar El Beida, Algiers (Algeria); Langdon, T.G. [Departments of Aerospace and Mechanical Engineering and Materials Science, University of Southern California, Los Angeles, CA 90089-1453 (United States); Materials Research Group, Faculty of Engineering and the Environment, University of Southampton, Southampton SO17 1BJ (United Kingdom)

    2014-03-01

    In situ synchrotron X-ray diffraction was used to study the decomposition kinetics of a metastable Cu–2.5Ni–0.6Si (wt%) alloy after severe plastic deformation by equal-channel angular pressing (ECAP) and high-pressure torsion (HPT). The measurements were performed at room temperature and also at high temperatures of 723, 823 and 973 K in order to determine the ageing effect after processing. Two forms of precipitates, namely δ-Ni{sub 2}Si and γ-Ni{sub 5}Si{sub 2}, were identified and the sequence of their appearance was well established for ECAP processing and ageing. There was no detection of either a modulated structure resulting from spinodal decomposition or an ordered structure nucleated from the modulated structure. An X-ray hybrid pixel array detector (XPAD-S140 detector) permitted the detection of the nucleation stages of the δ-Ni{sub 2}Si phase that began soon after 24 s of ageing at 723 K. There was also no trace of any amorphization of the matrix phase.

  20. Redetermination of the structure of the 80 K superconductor YBa2Cu4O8 by time-of-flight neutron powder diffraction

    International Nuclear Information System (INIS)

    Lightfoot, P.; Pei Shiyou; Jorgensen, J.D.; Yamada, Y.; Matsumoto, T.; Izumi, F.; Kodama, Y.

    1991-01-01

    M r =745.77, orthorhombic, Ammm, a=3.8402 (1), b=3.8708 (1), c=27.2309 (3) A, V=404.8 A 3 , D x =6.119 g cm -3 , Z=2, T=295 K, 912 reflections included, R wp =5.62%, R exp =3.34%. Rietveld analysis of high-resolution time-of-flight powder neutron diffraction data has been used to redetermine the structure of the 80 K superconductor YBa 2 Cu 4 O 8 (the '124 phase'). The essential features of the structure previously reported have been confirmed. This study improves upon the precision of the previously reported structural parameters, obtained by powder neutron diffraction. The compound is stoichiometric, with no occupancy of the O(5) inter-chain site. (orig.)

  1. A comparative study of the use of powder X-ray diffraction, Raman and near infrared spectroscopy for quantification of binary polymorphic mixtures of piracetam.

    Science.gov (United States)

    Croker, Denise M; Hennigan, Michelle C; Maher, Anthony; Hu, Yun; Ryder, Alan G; Hodnett, Benjamin K

    2012-04-07

    Diffraction and spectroscopic methods were evaluated for quantitative analysis of binary powder mixtures of FII(6.403) and FIII(6.525) piracetam. The two polymorphs of piracetam could be distinguished using powder X-ray diffraction (PXRD), Raman and near-infrared (NIR) spectroscopy. The results demonstrated that Raman and NIR spectroscopy are most suitable for quantitative analysis of this polymorphic mixture. When the spectra are treated with the combination of multiplicative scatter correction (MSC) and second derivative data pretreatments, the partial least squared (PLS) regression model gave a root mean square error of calibration (RMSEC) of 0.94 and 0.99%, respectively. FIII(6.525) demonstrated some preferred orientation in PXRD analysis, making PXRD the least preferred method of quantification. Copyright © 2012 Elsevier B.V. All rights reserved.

  2. Crystal structures of deuterated sodium molybdate dihydrate and sodium tungstate dihydrate from time-of-flight neutron powder diffraction.

    Science.gov (United States)

    Fortes, A Dominic

    2015-07-01

    Time-of-flight neutron powder diffraction data have been measured from ∼90 mol% deuterated isotopologues of Na2MoO4·2H2O and Na2WO4·2H2O at 295 K to a resolution of sin (θ)/λ = 0.77 Å(-1). The use of neutrons has allowed refinement of structural parameters with a precision that varies by a factor of two from the heaviest to the lightest atoms; this contrasts with the X-ray based refinements where precision may be > 20× poorer for O atoms in the presence of atoms such as Mo and W. The accuracy and precision of inter-atomic distances and angles are in excellent agreement with recent X-ray single-crystal structure refinements whilst also completing our view of the hydrogen-bond geometry to the same degree of statistical certainty. The two structures are isotypic, space-group Pbca, with all atoms occupying general positions, being comprised of edge- and corner-sharing NaO5 and NaO6 polyhedra that form layers parallel with (010) inter-leaved with planes of XO4 (X = Mo, W) tetra-hedra that are linked by chains of water mol-ecules along [100] and [001]. The complete structure is identical with the previously described molybdate [Capitelli et al. (2006 ▸). Asian J. Chem. 18, 2856-2860] but shows that the purported three-centred inter-action involving one of the water mol-ecules in the tungstate [Farrugia (2007 ▸). Acta Cryst. E63, i142] is in fact an ordinary two-centred 'linear' hydrogen bond.

  3. Quantitative Determination of Mineral Phases by the X-Ray Powder Diffraction Method in Organo-Mineral Substrates (Digestate, Compost and Ash From Biomass

    Directory of Open Access Journals (Sweden)

    Milan Geršl

    2014-01-01

    Full Text Available In the field of energetics and renewable energy sources, fertilizers, remediation and recultivation, waste management and other, biomass is widely studied and used these days. Determining the mineral phases present in the biomass is essential for determining the binding of chemical elements from which further derives its availability or unavailability for soil processes, plant nutrition or behaviour in technological processes. Semiquantitative phase analyses were carried out by the X-ray powder diffraction method (XRD.

  4. Phase transitions of Cu.sub.3+x./sub.Si observed by temperature-dependent x-ray powder diffraction

    Czech Academy of Sciences Publication Activity Database

    Correa, Cinthia Antunes; Poupon, Morgane; Kopeček, Jaromír; Král, Robert; Zemenová, Petra; Lecourt, J.; Barrier, N.; Brázda, Petr; Klementová, Mariana; Palatinus, Lukáš

    2017-01-01

    Roč. 91, Dec (2017), s. 129-139 ISSN 0966-9795 R&D Projects: GA ČR GC15-08842J Institutional support: RVO:68378271 Keywords : X-ray powder diffraction * differential scanning calorimetry * phase transitions * Cu3+xSi Subject RIV: BM - Solid Matter Physics ; Magnetism OBOR OECD: Condensed matter physics (including formerly solid state physics, supercond.) Impact factor: 3.140, year: 2016

  5. Determination of the cation distribution in Fe2Ni(PO4)2 using isotopic substitution and powder neutron diffraction

    International Nuclear Information System (INIS)

    Henry, P.F.; Weller, M.T.; Wilson, C.C.

    2003-01-01

    The distribution of divalent iron and nickel over the two metal sites with differing coordination geometry in Fe 2 Ni(PO 4 ) 2 , sarcopside, has been investigated using time-of-flight powder neutron diffraction of nickel isotopically substituted materials. Data from four separate samples were collected using HRPD at ISIS, containing nat Ni, 58 Ni, 60 Ni and 62 Ni, under identical conditions. The occupancy of iron on the M(1) site was found to be 0.290 (1) from a combined-data-set Rietveld refinement of the three isotopically substituted samples, compared with 0.26 (4) and 0.26 (15) respectively from this and a previous time-of-flight powder neutron diffraction study using natural-abundance nickel, and 0.366 (6) and 0.376 (3) using anomalous X-ray scattering techniques. A critical comparison of isotope substitution neutron diffraction and anomalous X-ray scattering methods for distinguishing nickel and iron from powder data is presented. (orig.)

  6. Neutron diffraction

    International Nuclear Information System (INIS)

    Heger, G.

    1996-01-01

    X-ray diffraction using conventional laboratory equipment and/or synchrotron installations is the most important method for structure analyses. The purpose of this paper is to discuss special cases, for which, in addition to this indispensable part, neutrons are required to solve structural problems. Even though the huge intensity of modern synchrotron sources allows in principle the study of magnetic X-ray scattering the investigation of magnetic structures is still one of the most important applications of neutron diffraction. (author) 15 figs., 1 tab., 10 refs

  7. Neutron diffraction

    Energy Technology Data Exchange (ETDEWEB)

    Heger, G. [Rheinisch-Westfaelische Technische Hochschule Aachen, Inst. fuer Kristallographie, Aachen (Germany)

    1996-12-31

    X-ray diffraction using conventional laboratory equipment and/or synchrotron installations is the most important method for structure analyses. The purpose of this paper is to discuss special cases, for which, in addition to this indispensable part, neutrons are required to solve structural problems. Even though the huge intensity of modern synchrotron sources allows in principle the study of magnetic X-ray scattering the investigation of magnetic structures is still one of the most important applications of neutron diffraction. (author) 15 figs., 1 tab., 10 refs.

  8. D2B, a new high resolution neutron powder diffractometer at ILL Grenoble

    International Nuclear Information System (INIS)

    Hewat, A.W.

    1987-01-01

    Applications of high resolution neutron powder diffraction to materials science have grown rapidly in the past 10 years, with the development of Rietveld methods of profile refinement, and new high resolution diffractometers and multidetectors. Materials studied range from catalysts to zeolites, and from battery electrodes to prestressed superconducting wires. Although the techniques have now been adapted for X-ray and synchrotron radiation, neutron powder diffraction retains unique advantages. In this paper we describe the design and first test measurements on the latest high resolution powder diffractometer D2B at ILL Grenoble. A review of the applications is published in Chemica Scripta (1986). (author) 9 refs., 6 figs., 2 tabs

  9. In situ powder X-ray diffraction, synthesis, and magnetic properties of the defect zircon structure ScVO(4-x).

    Science.gov (United States)

    Shafi, Shahid P; Kotyk, Matthew W; Cranswick, Lachlan M D; Michaelis, Vladimir K; Kroeker, Scott; Bieringer, Mario

    2009-11-16

    We report the formation pathway of ScVO(4) zircon from ScVO(3) bixbyite with emphasis on the synthesis and stability of the novel intermediate defect zircon phase ScVO(4-x) (0.0 situ powder X-ray diffraction. The oxidation of ScVO(3) to ScVO(4) involves two intermediates of composition ScVO(3.5+y) (0.00 diffraction, neutron diffraction, and bulk magnetic susceptibility data as well as (45)Sc and (51)V solid state NMR spectroscopy. ScVO(4-x) can only be obtained by oxidation of ScVO(3) or ScVO(3.5+y) while the reduction of ScVO(4) does not yield the novel defect structure. Mechanistic insights into the oxidative formation of ScVO(4) via the defect structure are presented.

  10. Reduction of Sr2MnO4 investigated by high temperature in situ neutron powder diffraction under hydrogen flow.

    Science.gov (United States)

    Broux, Thibault; Bahout, Mona; Hernandez, Olivier; Tonus, Florent; Paofai, Serge; Hansen, Thomas; Greaves, Colin

    2013-01-18

    This experiment emphasizes the first example of two-phase sequential Rietveld refinements throughout a solid/gas chemical reaction monitored by Neutron Powder Diffraction (NPD) at high temperature. The reduction of the n = 1 Ruddlesden-Popper (RP) oxide Sr(2)MnO(4) heated under a flow of 5% H(2)-He has been investigated throughout two heating/cooling cycles involving isothermal heating at 500 and 550 °C. Oxygen loss proceeds above T ∼ 470 °C and increases with temperature and time. When the oxygen deintercalated from the "MnO(2)" equatorial layers of the structure results in the Sr(2)MnO(3.69(2)) composition, the RP phase undergoes a first order I4/mmm → P2(1)/c, tetragonal to monoclinic phase transition as observed from time-resolved in situ NPD. The phase transition proceeds at 500 °C but is incomplete; the weight ratio of the P2(1)/c phase reaches ∼41% after 130 min of isothermal heating. The fraction of the monoclinic phase increases with increasing temperature and the phase transition is complete after 80 min of isothermal heating at 550 °C. The composition of the reduced material refined to Sr(2)MnO(3.55(1)) and does not vary on extended heating at 550 °C and subsequent cooling to room temperature (RT). The symmetry of Sr(2)MnO(3.55(1)) is monoclinic at 550 °C and therefore consistent with the RT structure determined previously for the Sr(2)MnO(3.64) composition obtained from ex situ reduction. Consequently, the stresses due to phase changes on heating/cooling in reducing atmosphere may be minimized. The rate constants for the reduction of Sr(2)MnO(4.00) determined from the evolution of weight ratio of the tetragonal and monoclinic phase in the time-resolved isothermal NPD data collected on the isotherms at 500 and 550 °C are k(500) = 0.110 × 10(-2) and k(550) = 0.516 × 10(-2) min(-1) giving an activation energy of ∼163 kJ mol(-1) for the oxygen deintercalation reaction.

  11. A novel technique combining high-resolution synchrotron x-ray microtomography and x-ray diffraction for characterization of micro particulates

    International Nuclear Information System (INIS)

    Merrifield, David R; Ramachandran, Vasuki; Roberts, Kevin J; Armour, Wesley; Axford, Danny; Basham, Mark; Connolley, Thomas; Evans, Gwyndaf; McAuley, Katherine E; Owen, Robin L; Sandy, James

    2011-01-01

    The processing of solids, such as crystals, is strongly influenced by the surface properties of the material. In recent years the pharmaceutical industry has shown great interest in identifying, or chemically speciating, the molecular components of crystal faces. Formerly, characterization of the molecular identity of crystal faces was restricted to the study of large single crystals. This would have been primarily for structure determination as part of the drug registration process. Diamond Light Source in Oxfordshire is a new synchrotron facility in the UK, having 18 operational beamlines with 4 more in the construction phase. Beamlines at this medium energy light source enable the study of micron-sized objects in great detail. It is well known that x-ray microtomography (XMT) can be used to investigate the external morphology of a crystal whereas x-ray diffraction (XRD) is used to study the molecular orientation, structure and packing within the crystal. The objective of this research is to assess the feasibility of, and thereby develop a new methodology for, characterizing the molecular identity of a particular face of a crystalline particle at a scale of scrutiny of 20–50 µm by combining these two powerful techniques. This work demonstrates the application of XMT and XRD to investigate respectively the shape and crystalline phase/orientation of relevant test crystals. This research has applications in the pharmaceutical industry in that when the exact molecular nature of a particular face is known, the important physico-pharmaceutical properties stemming from that can be better understood. Some initial data are presented and discussed

  12. Size-Strain Analysis of Iron-Excess Mn-Zn Ferrite Nanoparticles Using Synchrotron Diffraction and Its Correlation with Magnetic Saturation and Isoelectric pH.

    Science.gov (United States)

    Ichikawa, Rodrigo U; Parra, João P R L L; Martins, Murillo L; Yoshito, Walter K; Saeki, Margarida J; Turrillas, Xavier; Martinez, Luis G

    2018-08-01

    Iron-excess Mn-Zn ferrite nanoparticles were prepared by coprecipitation with sodium hydroxide (NaOH) at different concentrations (0.1, 0.2, 0.5 and 1.0 mol/L). The results of X-ray diffraction (XRD) analysis using Whole Powder Pattern Modeling (WPPM) showed that higher concentrations of NaOH promote crystallite growth and broader dispersion in crystallite sizes. Energy dispersive X-ray spectroscopy indicates that zinc loss is noticeable when [NaOH] ≥ 0.2 mol/L. XRD revealed also a significant less-crystalline phase contribution alongside the main peaks of the nanocrystalline cubic spinel ferrite phase. The less-crystalline fraction is lower for the ferrite obtained with 0.2 mol/L of NaOH, being about 50% and more than 70% for the other samples. Despite of the less-crystalline fraction and the excess of iron, no secondary phases were detected. The Warren curves showed that the concentration of NaOH significantly influences the microstrain in the crystallites, being smaller for the sample obtained with NaOH at 0.2 mol/L. The sample prepared with this condition presented the better properties to be used as magnetic tracer in clinical diagnoses combining small mean crystallite size, low microstrain, which resulted in materials with higher magnetic saturation and high surface charge under blood pH.

  13. An in situ time-of-flight neutron powder diffraction study of the humidity-induced phase transition in sodium monothiophosphate

    International Nuclear Information System (INIS)

    Takas, Nathan J.; Aitken, Jennifer A.

    2007-01-01

    Anhydrous β-Na 3 PO 3 S, obtained by rapid cooling, has been observed to convert to the more thermodynamically stable, anhydrous α-Na 3 PO 3 S upon exposure to a humid atmosphere. Though water plays a critical role in this polymorphic transformation, it is absent in both the initial and final materials. In situ time-of-flight neutron powder diffraction was used to track the progress of this transition as a function of time. Diffraction data were acquired using the Intense Pulsed Neutron Source (IPNS) at Argonne National Laboratory. An empirical whole pattern fitting method was used to determine the polymorphic phase composition over time. The resulting data were evaluated using several solid-state kinetic models. The kinetics of this transition has been determined to be best described by either one- or two-dimensional diffusion. The significance of these models with respect to the physical phenomenon is discussed. - Graphical abstract: Anhydrous β-Na 3 PO 3 S has been observed to convert to anhydrous α-Na 3 PO 3 S upon exposure to a humid atmosphere. In situ neutron powder diffraction was used to monitor the transition. A whole pattern fitting method was used to determine the phase composition, as a function of time. The data were evaluated using several solid-state kinetic models

  14. Crystal structure of the quaternary compound CuTa{sub 2}InTe{sub 4} from X-ray powder diffraction

    Energy Technology Data Exchange (ETDEWEB)

    Delgado, G.E. [Laboratorio de Cristalografia, Departamento de Quimica, Facultad de Ciencias, Universidad de Los Andes, Merida 5101 (Venezuela, Bolivarian Republic of)], E-mail: gerzon@ula.ve; Mora, A.J. [Laboratorio de Cristalografia, Departamento de Quimica, Facultad de Ciencias, Universidad de Los Andes, Merida 5101 (Venezuela, Bolivarian Republic of); Grima-Gallardo, P.; Munoz, M.; Duran, S.; Quintero, M. [Centro de Estudios de Semiconductores, Departamento de Fisica, Facultad de Ciencias, Universidad de Los Andes, Merida 5101 (Venezuela, Bolivarian Republic of)

    2008-09-01

    The crystal structure of the new quaternary compound CuTa{sub 2}InTe{sub 4} was studied using X-ray powder diffraction data. The powder pattern refined by the Rietveld method indicates that this material crystallizes in the tetragonal system with space group I-4-bar 2m (No. 121), Z=2, and unit cell parameters a=6.1963(2) A, c=12.4164(4) A, c/a=2.00 and V=476.72(3) A{sup 3}. The structural and instrumental refinement of 28 parameters led to R{sub p}=10.4%, R{sub wp}=11.1%, R{sub exp}=6.8% and {chi}{sup 2}=2.7 for 96 independent reflections.

  15. L-Lysine: exploiting powder X-ray diffraction to complete the set of crystal structures of the 20 directly encoded proteinogenic amino acids.

    Science.gov (United States)

    Williams, P Andrew; Hughes, Colan E; Harris, Kenneth D M

    2015-03-23

    During the last 75 years, crystal structures have been reported for 19 of the 20 directly encoded proteinogenic amino acids in their natural (enantiomerically pure) form. The crystal structure is now reported for the final member of this set: L-lysine. As crystalline L-lysine has a strong propensity to incorporate water under ambient atmospheric conditions to form a hydrate phase, the pure (non-hydrate) crystalline phase can be obtained only by dehydration under rigorously anhydrous conditions, resulting in a microcrystalline powder sample. For this reason, modern powder X-ray diffraction methods have been exploited to determine the crystal structure in this final, elusive case. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  16. 1-(2-furoyl)-3,3-(diphenyl)thiourea: spectroscopic characterization and structural study from X-ray powder diffraction using simulated annealing

    Energy Technology Data Exchange (ETDEWEB)

    Estevez H, O.; Duque, J. [Universidad de La Habana, Instituto de Ciencia y Tecnologia de Materiales, 10400 La Habana (Cuba); Rodriguez H, J. [UNAM, Instituto de Investigaciones en Materiales, 04510 Mexico D. F. (Mexico); Yee M, H., E-mail: oestevezh@yahoo.com [Instituto Politecnico Nacional, Escuela Superior de Fisica y Matematicas, 07738 Mexico D. F. (Mexico)

    2015-07-01

    1-Furoyl-3,3-diphenylthiourea (FDFT) was synthesized, and characterized by Ftir, {sup 1}H and {sup 13}C NMR and ab initio X-ray powder structure analysis. FDFT crystallizes in the monoclinic space group P2{sub 1} with a = 12.691(1), b = 6.026(2), c = 11.861(1) A, β = 117.95(2) and V = 801.5(3) A{sup 3}. The crystal structure has been determined from laboratory X-ray powder diffraction data using direct space global optimization strategy (simulated annealing) followed by the Rietveld refinement. The thiourea group makes a dihedral angle of 73.8(6) with the furoyl group. In the crystal structure, molecules are linked by van der Waals interactions, forming one-dimensional chains along the a axis. (Author)

  17. Temperature induced phase transformations and microstructural changes in nanostructured FeCu solid solutions using in situ neutron powder thermo-diffraction

    Energy Technology Data Exchange (ETDEWEB)

    Martinez-Blanco, D. [Unidad de Magnetometria, SCT' s, Universidad de Oviedo, Julian Claveria, 8, 33006 Oviedo (Spain); Departamento de Fisica, Universidad de Oviedo, Calvo Sotelo s/n, Oviedo 33007 (Spain); Gorria, P., E-mail: pgorria@uniovi.e [Departamento de Fisica, Universidad de Oviedo, Calvo Sotelo s/n, Oviedo 33007 (Spain); Blanco, J.A. [Departamento de Fisica, Universidad de Oviedo, Calvo Sotelo s/n, Oviedo 33007 (Spain); Smith, R.I. [ISIS facility, RAL, Chilton, Didcot, Oxon OX11 0QX (United Kingdom)

    2009-08-26

    In situ neutron powder thermo-diffraction experiments in the temperature range from 300 K to 1170 K have been carried out in nanostructured and metastable Fe{sub 15}Cu{sub 85} and Fe{sub 85}Cu{sub 15} solid solutions, which were synthesized by means of a mechanical alloying technique. We report on the microstructural changes and the phase transformations that take place during controlled heating and cooling processes. The average crystalline grain size is similar for both samples in the as-milled state (approx16-20 nm) while the induced strain is 2.5 times higher in the Fe-rich powders, reaching 1%. Moreover, the alpha-gamma transformation for Fe{sub 15}Cu{sub 85} starts at temperatures lower (approx900 K) than that expected for pure Fe (1183 K) due likely to the existence of local inhomogeneities in the composition of the ball milled material.

  18. Neutron Powder Diffraction Measurements of the Spinel MgGa 2 O 4 :Cr 3+ - A Comparative Study between the High Flux Diffractometer D2B at the ILL and the High Resolution Powder Diffractometer Aurora at IPEN

    DEFF Research Database (Denmark)

    Silva, M A F M da; Sosman, L P; Yokaichiya, F

    2012-01-01

    and MgGa 2 O 4 and relate structural changes observed in MgGa 2 O 4 -Ga 2 O 3 system to the optical properties, and secondly, to compare the neutron powder diffraction results obtained using two diffractometers: D2B located at the ILL (Grenoble, France) and Aurora located at IPEN (São Paulo, Brazil......Optical materials that emit from the visible to the near-infrared spectral region are of great interest due to their possible application as tunable radiation sources, as signal transmission, display, optoelectronics signal storage, cellulose industry as well as in dosimetry. One important family...

  19. The stoichiometry of synthetic alunite as a function of hydrothermal ageing investigated by solid-state NMR spectroscopy, powder X-ray diffraction, and infrared spectroscopy

    DEFF Research Database (Denmark)

    Grube, Elisabeth; Nielsen, U. G.

    2014-01-01

    The stoichiometry of a series of synthetic alunite (nominally KAl3(SO4)2(OH)6) samples prepared by hydrothermal methods as a function of reaction time (1 – 31 days) has been investigated by powder X-ray diffraction, Fourier transform infrared spectroscopy as well as solid-state 1H and 27Al magic...... of potassium defects present, from 17.261(1) to 17.324(5) Å. Solid-state 27Al MAS NMR revealed a decrease in the defect concentration as a function of time and showed the presence of 7-10 % impurities in the samples....

  20. Structure of superconducting Sr0.9La0.1CuO2 (Tc=42 K) from neutron powder diffraction

    International Nuclear Information System (INIS)

    Jorgensen, J.D.; Radaelli, P.G.; Hinks, D.G.; Wagner, J.L.; Kikkawa, S.; Er, G.; Kanamaru, F.

    1993-01-01

    We have refined the crystal structure of the electron-doped infinite-layer superconducting compound Sr 0.9 La 0.1 CuO 2 (T c =42 K) from neutron-powder-diffraction data for an 82-mg sample synthesized at high pressure. The metal- and oxygen-atom lattices are perfectly stoichiometric and there is no excess (interstitial) oxygen in the Sr(La) layer. Thus, neither oxygen vacancies nor interstitial oxygen play a role in the doping of this compound

  1. Disorder in the composite crystal structure of the manganese `disilicide' MnSi1.73 from powder X-ray diffraction data.

    Science.gov (United States)

    Akselrud, L; Cardoso Gil, R; Wagner-Reetz, M; Grin, Yu

    2015-12-01

    The crystal structure of the higher manganese silicide MnSi1.7 (known in the literature as HMS) is investigated in samples with different compositions obtained by different techniques at temperatures not higher than 1273 K. Powder X-ray diffraction was applied. The crystal structure is described as incommensurate composite. In addition to the ordered model already known in the literature, the partial disorder in the silicon substructure was detected and described introducing an additional atomic site with a different modulation function.

  2. A general method for baseline-removal in ultrafast electron powder diffraction data using the dual-tree complex wavelet transform

    Directory of Open Access Journals (Sweden)

    Laurent P. René de Cotret

    2017-07-01

    Full Text Available The general problem of background subtraction in ultrafast electron powder diffraction (UEPD is presented with a focus on the diffraction patterns obtained from materials of moderately complex structure which contain many overlapping peaks and effectively no scattering vector regions that can be considered exclusively background. We compare the performance of background subtraction algorithms based on discrete and dual-tree complex (DTCWT wavelet transforms when applied to simulated UEPD data on the M1–R phase transition in VO2 with a time-varying background. We find that the DTCWT approach is capable of extracting intensities that are accurate to better than 2% across the whole range of scattering vector simulated, effectively independent of delay time. A Python package is available.

  3. Light source for synchrotron radiation x-ray topography study at Beijing Synchrotron Radiation Laboratory (BSRL)

    International Nuclear Information System (INIS)

    Zhao Jiyong; Jiang Jianhua; Tian Yulian

    1992-01-01

    Characteristics of the synchrotron radiation source for X-ray topography study at Beijing Synchrotron Radiation Laboratory (BSRL) is described, local geometrical resolution of topographies is discussed, and the diffracting intensities of white beam topography is given

  4. Advanced development of catalysts by using the high-brilliance synchrotron radiation in SPring-8

    International Nuclear Information System (INIS)

    2006-10-01

    The advanced development of catalysts by using the high-brilliance synchrotron radiation in SPring-8 is described: (1) the industrial use of SPring-8, (2) the analytical methods of catalyst using SPring-8 (XAFS, powder X-ray diffraction, thin film X-ray scattering, X-ray imaging, infrared analysis, X-ray fluorescence analysis, and photoelectron spectroscopy etc.), (3) the history of synchrotron radiation and catalyst investigations, (4) the new advanced measuring methods of catalyst using synchrotron radiation (various X-ray spectroscopic methods, and application of XAFS to highly-disperse systems of catalyst), and (5) the new advanced development of catalysts using synchrotron radiation and its applications (motor-car catalysts, light catalysts, fuel cells, nanotechnology, and trace amounts of catalyst in wastes). (M.H.)

  5. High-pressure synchrotron Mössbauer and X-ray diffraction studies: Exploring the structure-related valence fluctuation in EuNi{sub 2}P{sub 2}

    Energy Technology Data Exchange (ETDEWEB)

    Li, Chunyu [Center for High Pressure Science and Technology Advanced Research, Shanghai 201203 (China); Natural Science Research Center, Academy of Fundamental and Interdisciplinary Sciences, Harbin Institute of Technology, Harbin 150080 (China); Yu, Zhenhai, E-mail: yuzh@hpstar.ac.cn [Center for High Pressure Science and Technology Advanced Research, Shanghai 201203 (China); Natural Science Research Center, Academy of Fundamental and Interdisciplinary Sciences, Harbin Institute of Technology, Harbin 150080 (China); Bi, Wenli [Advanced Photon Source, Argonne National Laboratory, Argonne, IL 60439 (United States); Department of Geology, University of Illinois at Urbana-Champaign, Urbana, IL 61801 (United States); Zhao, Jiyong; Hu, Michael Y. [Advanced Photon Source, Argonne National Laboratory, Argonne, IL 60439 (United States); Zhao, Jinggeng [Natural Science Research Center, Academy of Fundamental and Interdisciplinary Sciences, Harbin Institute of Technology, Harbin 150080 (China); Wu, Wei [Beijing National Lab for Condensed Matter Physics, Institute of Physics, Chinese Academy of Sciences, Beijing 100190 (China); Luo, Jianlin [Beijing National Lab for Condensed Matter Physics, Institute of Physics, Chinese Academy of Sciences, Beijing 100190 (China); Collaborative Innovation Center of Quantum Matter, Beijing 100190 (China); Yan, Hao, E-mail: yanhao@hpstar.ac.cn [Center for High Pressure Science and Technology Advanced Research, Shanghai 201203 (China); Alp, Esen E. [Advanced Photon Source, Argonne National Laboratory, Argonne, IL 60439 (United States); Liu, Haozhe, E-mail: haozhe.liu@hpstar.ac.cn [Center for High Pressure Science and Technology Advanced Research, Shanghai 201203 (China); Natural Science Research Center, Academy of Fundamental and Interdisciplinary Sciences, Harbin Institute of Technology, Harbin 150080 (China)

    2016-11-15

    The high-pressure effect on valence fluctuation of the ThCr{sub 2}Si{sub 2}-type intermetallic compound EuNi{sub 2}P{sub 2} has been investigated using in situ synchrotron Mössbauer spectroscopy (SMS). The isomer shift of {sup 151}Eu in EuNi{sub 2}P{sub 2} increases monotonically with increasing pressure up to 50 GPa, suggesting a valence transition of the Eu from mixed toward trivalent. The synchrotron angle-dispersive X-ray diffraction (AD-XRD) experiment shows that EuNi{sub 2}P{sub 2} remains in the tetragonal structure up to 32.5 GPa at room temperature. We propose that the evolutions of bonding distance with pressure have an obvious effect on the valence fluctuation.

  6. Resolution of crystal structures by X-ray and neutrons powder diffraction using global optimisation methods; Resolution des structures cristallines par diffraction des rayons X et neutrons sur poudres en utilisant les methodes d'optimisation globale

    Energy Technology Data Exchange (ETDEWEB)

    Palin, L

    2005-03-15

    We have shown in this work that X-ray diffraction on powder is a powerful tool to analyze crystal structure. The purpose of this thesis is the resolution of crystal structures by X-ray and neutrons diffraction on powder using global optimisation methods. We have studied 3 different topics. The first one is the order-disorder phenomena observed in some globular organic molecular solids. The second is the opiate family of neuropeptides. These neurotransmitters regulate sensory functions including pain and control of respiration in the central nervous system. The aim of our study was to try to determine the crystal structure of Leu-enkephalin and some of its sub-fragments. The determination of the crystal structures has been done performing Monte Carlo simulations. The third one is the location of benzene in a sodium-X zeolite. The zeolite framework was already known and the benzene has been localized by simulated annealing and by the use of maximum entropy maps.

  7. SUNY beamline facilities at the National Synchrotron Light Source (Final Report)

    Energy Technology Data Exchange (ETDEWEB)

    Coppens, Philip

    2003-06-22

    The DOE sponsored SUNY synchrotron project has involved close cooperation among faculty at several SUNY campuses. A large number of students and postdoctoral associates have participated in its operation which was centered at the X3 beamline of the National Synchrotron Light Source at Brookhaven National Laboratory. Four stations with capabilities for Small Angle Scattering, Single Crystal and Powder and Surface diffraction and EXAFS were designed and operated with capability to perform experiments at very low as well as elevated temperatures and under high vacuum. A large amount of cutting-edge science was performed at the facility, which in addition provided excellent training for students and postdoctoral scientists in the field.

  8. SUNY beamline facilities at the National Synchrotron Light Source (Final Report)

    International Nuclear Information System (INIS)

    Coppens, Philip

    2003-01-01

    The DOE sponsored SUNY synchrotron project has involved close cooperation among faculty at several SUNY campuses. A large number of students and postdoctoral associates have participated in its operation which was centered at the X3 beamline of the National Synchrotron Light Source at Brookhaven National Laboratory. Four stations with capabilities for Small Angle Scattering, Single Crystal and Powder and Surface diffraction and EXAFS were designed and operated with capability to perform experiments at very low as well as elevated temperatures and under high vacuum. A large amount of cutting-edge science was performed at the facility, which in addition provided excellent training for students and postdoctoral scientists in the field

  9. Development of a high temperature unicam camera and application to X-ray diffraction on powdered uranium

    International Nuclear Information System (INIS)

    Laugier, J.; Blum, P.L.; Debrenne, P.

    1964-01-01

    A high temperature commercial X-ray camera (UNICAM S150), modified in order to improve some of its performances, is adapted to the uranium powder problem. The strong uranium reactivity for oxygen and silica, the sintering and the grain growth in β-phase are avoided. X-ray photographs are thus possible even in the γ-phase. (authors) [fr

  10. Thermal expansion of kyanite at ambient pressure: An X-ray powder diffraction study up to 1000 °C

    Directory of Open Access Journals (Sweden)

    Xi Liu

    2010-10-01

    Full Text Available The thermal expansion coefficients of kyanite at ambient pressure have been investigated by an X-ray powder diffraction technique with temperatures up to 1000 °C. No phase transition was observed in the experimental temperature range. Data for the unit-cell parameters and temperatures were fitted empirically resulting in the following thermal expansion coefficients: αa = 5.8(3 × 10−5, αb = 5.8(1 × 10−5, αc = 5.2(1 × 10−5, and αV = 7.4(1 × 10−3 °C−1, in good agreement with a recent neutron powder diffraction study. On the other hand, the variation of the unit-cell angles α, β and γ of kyanite with increase in temperature is very complicated, and the agreement among all studies is poor. The thermal expansion data at ambient pressure reported here and the compression data at ambient temperature from the literature suggest that, for the kyanite lattice, the most and least thermally expandable directions correspond to the most and least compressible directions, respectively.

  11. High-resolution inelastic neutron scattering and neutron powder diffraction study of the adsorption of dihydrogen by the Cu(II) metal–organic framework material HKUST-1

    Energy Technology Data Exchange (ETDEWEB)

    Callear, Samantha K.; Ramirez-Cuesta, Anibal J.; David, William I.F. [ISIS Facility, Rutherford Appleton Laboratory, Harwell Science and Innovation Campus, Didcot, OX11 0QX (United Kingdom); Millange, Franck [Institut Lavoisier Versailles (CNRS UMR 8180), Université de Versailles, 78035 Versailles (France); Walton, Richard I., E-mail: r.i.walton@warwick.ac.uk [Department of Chemistry, University of Warwick, CV4 7AL, Coventry (United Kingdom)

    2013-12-12

    Highlights: • Binding sites for dihydrogen in a metal–organic framework have been identified. • The combination of diffraction and spectroscopy shows competitive filling of various adsorption sites. • Inelastic neutron scattering over wide-momentum transfer reveals new models for hydrogen-framework interactions. - Abstract: We present new high-resolution inelastic neutron scattering (INS) spectra (measured using the TOSCA and MARI instruments at ISIS) and powder neutron diffraction data (measured on the diffractometer WISH at ISIS) from the interaction of the prototypical metal–organic framework HKUST-1 with various dosages of dihydrogen gas. The INS spectra show direct evidence for the sequential occupation of various distinct sites for dihydrogen in the metal–organic framework, whose population is adjusted during increasing loading of the guest. The superior resolution of TOSCA reveals subtle features in the spectra, not previously reported, including evidence for split signals, while complementary spectra recorded on MARI present full information in energy and momentum transfer. The analysis of the powder neutron patterns using the Rietveld method shows a consistent picture, allowing the crystallographic indenisation of binding sites for dihydrogen, thus building a comprehensive picture of the interaction of the guest with the nanoporous host.

  12. High temperature neutron powder diffraction study of the Cu12Sb4S13 and Cu4Sn7S16 phases

    Science.gov (United States)

    Lemoine, Pierric; Bourgès, Cédric; Barbier, Tristan; Nassif, Vivian; Cordier, Stéphane; Guilmeau, Emmanuel

    2017-03-01

    Ternary copper-containing sulfides Cu12Sb4S13 and Cu4Sn7S16 have attracted considerable interest since few years due to their high-efficiency conversion as absorbers for solar energy and promising thermoelectric materials. We report therein on the decomposition study of Cu12Sb4S13 and Cu4Sn7S16 phases using high temperature in situ neutron powder diffraction. Our results obtained at a heating rate of 2.5 K/min indicate that: (i) Cu12Sb4S13 decomposes above ≈792 K into Cu3SbS3, and (ii) Cu4Sn7S16 decomposes above ≈891 K into Sn2S3 and a copper-rich sulfide phase of sphalerite ZnS-type structure with an assumed Cu3SnS4 stoichiometry. Both phase decompositions are associated to a sulfur volatilization. While the results on Cu12Sb4S13 are in fair agreement with recent published data, the decomposition behavior of Cu4Sn7S16 differs from other studies in terms of decomposition temperature, thermal stability and products of reaction. Finally, the crystal structure refinements from neutron powder diffraction data are reported and discussed for the Cu4Sn7S16 and tetrahedrite Cu12Sb4S13 phases at 300 K, and for the high temperature form of skinnerite Cu3SbS3 at 843 K.

  13. Structural and Thermal Characterization of Zolpidem Hemitartrate Hemihydrate (Form E) and Its Decomposition Products by Laboratory X-Ray Powder Diffraction

    Energy Technology Data Exchange (ETDEWEB)

    Halasz, I.; Dinnebier, R

    2010-01-01

    The crystal structure of zolpidem hemitartrate hemihydrate (I, Form E) has been solved from high-resolution laboratory powder diffraction data. It crystallizes in the orthorhombic P2{sub 1}2{sub 1}2{sub 1} space group with a = 22.4664(6) {angstrom}, b = 26.0420(7) {angstrom}, and c = 7.4391(1) {angstrom}. Protonation of zolpidem molecules could not be unambiguously determined. Thermal stability of Form E has been investigated by TG-DTA and in situ by temperature resolved X-ray powder diffraction. Water loss occurs between 50 C {le} t {le} 100 C while structure decomposition commences at approximately 120 C yielding zolpidem tartrate (II) and pure zolpidem base (III) in approximately equimolar amounts. Crystal structures of II and III have been solved simultaneously from a single powder pattern of thermally decomposed I. Zolpidem tartrate crystallizes in the orthorhombic P2{sub 1}2{sub 1}2{sub 1} space group with a = 19.9278(8) {angstrom}, b = 15.1345(8) {angstrom}, and c = 7.6246(2) {angstrom} (at 140 C). Zolpidem base crystallizes in the orthorhombic Pcab space group with a = 9.9296(4) {angstrom}, b = 18.4412(9) {angstrom}, and c = 18.6807(9) {angstrom} (at 140 C). In the reported crystal structures zolpidem molecules form stacks through {pi}-{pi} interaction or dipole-dipole interactions while tartrate moieties, if present, form hydrogen bonded chains. Water molecule in I forms a hydrogen bond to the imidazole nitrogen atom of the zolpidem molecule. Free space in the crystal structure of I could allow for the additional water molecules and thus a variable water content.

  14. Structural Transitions in Nanosized Zn0.97Al0.03O Powders under High Pressure Analyzed by in Situ Angle-Dispersive X-ray Diffraction

    Directory of Open Access Journals (Sweden)

    Chih-Ming Lin

    2016-07-01

    Full Text Available Nanosized aluminum-doped zinc oxide Zn1−xAlxO (AZO powders (AZO-NPs with x = 0.01, 0.03, 0.06, 0.09 and 0.11 were synthesized by chemical precipitation method. The thermogravimetric analysis (TGA indicated that the precursors were converted to oxides from hydroxides near 250 °C, which were then heated to 500 °C for subsequent thermal processes to obtain preliminary powders. The obtained preliminary powders were then calcined at 500 °C for three hours. The structure and morphology of the products were measured and characterized by angle-dispersive X-ray diffraction (ADXRD and scanning electron microscopy (SEM. ADXRD results showed that AZO-NPs with Al content less than 11% exhibited würtzite zinc oxide structure and there was no other impurity phase in the AZO-NPs, suggesting substitutional doping of Al on Zn sites. The Zn0.97Al0.03O powders (A3ZO-NPs with grain size of about 21.4 nm were used for high-pressure measurements. The in situ ADXRD measurements revealed that, for loading run, the pressure-induced würtzite (B4-to-rocksalt (B1 structural phase transition began at 9.0(1 GPa. Compared to the predicted phase-transition pressure of ~12.7 GPa for pristine ZnO nanocrystals of similar grain size (~21.4 nm, the transition pressure for the present A3ZO-NPs exhibited a reduction of ~3.7 GPa. The significant reduction in phase-transition pressure is attributed to the effects of highly selective site occupation, namely Zn2+ and Al3+, were mainly found in tetrahedral and octahedral sites, respectively.

  15. Crystal structure of aspartame anhydrate from powder diffraction data. Structural aspects of the dehydration process of aspartame

    NARCIS (Netherlands)

    Guguta, C.; Meekes, H.L.M.; Gelder, R. de

    2006-01-01

    Aspartame has three pseudo-polymorphic forms, two hydrates and a hemi-hydrate, for which crystal structures were determined from single-crystal diffraction data. This paper presents the crystal structure of the anhydrate, which was obtained by dehydrating the hemi-hydrate. The crystal structure of

  16. High-pressure single-crystal synchrotron X-ray diffraction of kainite (KMg(SO4) Cl 3H2O)

    Science.gov (United States)

    Nazzareni, S.; Comodi, P.; Hanfland, M.

    2018-03-01

    Kainite (KMg(SO4) Cl 3H2O) is a "mixed-salt" sulfate from the group of evaporitic minerals more soluble than Ca-sulfate hydrate and NaCl. The compressibility and structural modifications of monoclinic (sp. gr. C2/m) kainite up to a pressure of 14 GPa were studied by high-pressure single-crystal synchrotron X-ray diffraction. Kainite remains stable over the investigated pressure range and no phase transition was recognised. The bulk modulus is K 0 = 31.6 (1) GPa, with K' fixed to 4, as obtained by fitting the P-volume data with a second-order Birch-Murnaghan EoS (BM2); instead of using a BM3 EoS, we obtained K 0 = 32.2(5) GPa, K' =3.8 (1). The linear moduli calculated for the lattice parameters fitting the data with a BM3 EoS are for a-axis M 0a = 117(4) GPa, Mpa = 11(1), for b-axis M 0b = 113(2) GPa, Mpc = 8.6(5), and c-axis M 0c = 68.2(3) GPa, Mpc = 14(1). Structure refinements showed a strong compression of the K polyhedra and in particular K(1) and K(3) polyhedra have similar polyhedral bulk moduli: K 0K(1) = 20.8(7) GPa, K'=4.8(3); K 0K(2) = 29(1) GPa, K'=8.1(6); K 0K(3) = 26(1) GPa, K'=4.2(4). The most compressible bond distances are K(1)-Cl(2) with a shortening of about 13%, K(1)-Cl(1) with a shortening of about 10%, K(3)-Ow(6) and K(3)-O8(B) both with a shortening of 9%. S-tetrahedra are almost incompressible and Mg-octahedra bulk moduli are K 0Mg(2) = 102(4) GPa, and K 0Mg(4) = 72(1) GPa, K 0Mg(1) = 41(4) GPa K'= 8.9(1.7), and K 0Mg(3) = 65(5) GPa K'= 10(2). The strain tensor analysis indicates that the most compressible direction of the kainite monoclinic structure is oriented 29.7(2)° from the c-axis in the (0 1 0) plane. The shortening of the K(1)-K(2) distance (from 4.219(4) Å at ambient P to 3.521(7) Å at 11.9 GPa) and the different compressibilities of the octahedra/tetrahedra may explain why the stiffer direction of kainite is in the a-c plane approximatively along the direction where K(1)-K(2) and Mg(4)-Mg(3)-Mg(4) polyhedra align. This may

  17. In situ neutron powder diffraction of the formation of SrGa2D2, and hydrogenation behavior of YbGa2 and EuGa2.

    Science.gov (United States)

    Wenderoth, Patrick; Kohlmann, Holger

    2013-09-16

    The hydrogenation behavior of the Zintl phases MGa2 (M = Sr, Eu, Yb) was investigated. Upon being heated under 50 bar of hydrogen gas pressure, SrGa2 starts forming the polyanionic hydride SrGa2H2 at 125 °C as observed by in situ differential scanning calorimetry (DSC) and ex situ X-ray powder diffraction. The deuteration of SrGa2 was studied by in situ neutron powder diffraction at temperatures up to 300 °C in the pressure range of 50 ≤ p(D2) ≤ 61 bar with a time resolution of two minutes. Neither incorporation of deuterium into the interstitials of the crystal structure of SrGa2 nor any other intermediate of the reaction was observed. No significant variation in positional or occupational parameters as refined by the Rietveld method was observed for the deuteride SrGa2D2 under various temperature and pressure conditions (e.g., at T = 299 °C, p(D2) = 60 bar, space group P3m1, a = 4.4098(2) Å, c = 4.7429(3) Å, Sr in 1a, 0 0 0; Ga in 2d, 1/3 2/3 0.474(1); D in 2d, 1/3 2/3 0.120(2)). In situ DSC complemented by ex situ X-ray powder diffraction revealed that EuGa2 and YbGa2 do not form polyanionic hydrides in the investigated temperature-pressure ranges (20 °C ≤ T ≤ 220 °C, 5 bar ≤ p ≤ 54 bar). Instead binary hydrides and gallium-rich intermetallics are formed. The first refined crystal structural data are presented for YbGa6 in the tetragonal PuGa6-type structure (space group P4/nbm (No. 125), a = 6.0890(3) Å, c = 7.6562(4) Å, Yb in 2c, 3/4 1/4 0; Ga1 in 8m, 0.4750(4) 0.5250(4) 0.3377(4); Ga2 in 4g, 1/4 1/4 0.1691(5)).

  18. In situ synchrotron X-ray diffraction studies of the effect of microstructure on tensile behavior and retained austenite stability of thermo-mechanically processed transformation induced plasticity steel

    Energy Technology Data Exchange (ETDEWEB)

    Yan, Kun [School of Mechanical, Materials and Mechatronic Engineering, University of Wollongong, NSW 2522 (Australia); Liss, Klaus-Dieter [School of Mechanical, Materials and Mechatronic Engineering, University of Wollongong, NSW 2522 (Australia); Australian Nuclear Science and Technology Organisation, Lucas Heights, NSW 2234 (Australia); Timokhina, Ilana B. [Institute for Frontier Materials, Deakin University, Geelong, VIC 3217 (Australia); Pereloma, Elena V., E-mail: elenap@uow.edu.au [School of Mechanical, Materials and Mechatronic Engineering, University of Wollongong, NSW 2522 (Australia)

    2016-04-26

    Transmission electron microscopy and in situ synchrotron high-energy X-ray diffraction were used to investigate the martensitic transformation and lattice strains under uniaxial tensile loading of Fe-Mn-Si-C-Nb-Mo-Al Transformation Induced Plasticity (TRIP) steel subjected to different thermo-mechanical processing schedules. In contrast with most of the diffraction analysis of TRIP steels reported previously, the diffraction peaks from the martensite phase were separated from the peaks of the ferrite-bainite α-matrix. The volume fraction of retained γ-austenite, as well as the lattice strain, were determined from the diffraction patterns recorded during tensile deformation. Although significant austenite to martensite transformation starts around the macroscopic yield stress, some austenite grains had already experienced martensitic transformation. Hooke’s Law was used to calculate the phase stress of each phase from their lattice strain. The ferrite-bainite α-matrix was observed to yield earlier than austenite and martensite. The discrepancy between integrated phase stresses and experimental macroscopic stress is about 300 MPa. A small increase in carbon concentration in retained austenite at the early stage of deformation was detected, but with further straining a continuous slight decrease in carbon content occurred, indicating that mechanical stability factors, such as grain size, morphology and orientation of the retained austenite, played an important role during the retained austenite to martensite transformation.

  19. Twin-domain size and bulk oxygen in-diffusion kinetics of YBa2Cu3O6+x studied by neutron powder diffraction and gas volumetry

    DEFF Research Database (Denmark)

    Poulsen, H.F.; Andersen, N.H.; Lebech, B.

    1991-01-01

    We report experimental results of twin-domain size and bulk oxygen in-diffusion kinetics of YBa2Cu3O6+x, which supplement a previous and simultaneous study of the structural phase diagram and oxygen equilibrium partial pressure. Analysis of neutron powder diffraction peak broadening show features...... which are identified to result from temperature independent twin-domain formation in to different orthorhombic phases with domain sizes 250 and 350 angstrom, respectively. The oxygen in-diffusion flow shows simple relaxation type behaviour J = J0 exp(-t/tau) despite a rather broad particle size...... distribution. At higher temperatures, tau is activated with activation energies 0.55 and 0.25 eV in the tetragonal and orthorhombic phases, respectively. Comparison between twin-domain sizes and bulk oxygen in-diffusion time constants indicates that the twin-domain boundaries may contribute to the effective...

  20. Magnetoelastic effects in Jahn-Teller distorted CrF2 and CuF2 studied by neutron powder diffraction

    International Nuclear Information System (INIS)

    Chatterji, Tapan; Hansen, Thomas C

    2011-01-01

    We have studied the temperature dependence of the crystal and magnetic structures of the Jahn-Teller distorted transition metal difluorides CrF 2 and CuF 2 by neutron powder diffraction in the temperature range 2-280 K. The lattice parameters and the unit cell volume show magnetoelastic effects below the Neel temperature. The lattice strain due to the magnetostriction effect couples with the square of the order parameter of the antiferromagnetic phase transition. We also investigated the temperature dependence of the Jahn-Teller distortion, which does not show any significant effect at the antiferromagnetic phase transition but increases linearly with increasing temperature for CrF 2 , and remains almost independent of temperature in CuF 2 . The magnitude of magnetovolume effect seems to increase with the low temperature saturated magnetic moment of the transition metal ions but the correlation is not at all perfect.

  1. Structure of deuteride of a null matrix Ti-Mo alloy studied by complementation of neutron and X-ray powder diffraction

    International Nuclear Information System (INIS)

    Wu, E.; Yuan, X.Z.; Liu, S.; Guo, L.P.; Sun, K.

    2006-01-01

    The detailed structural information of the deuteride of a null matrix Ti-Mo alloy containing 33 at.% of Mo is studied by complementation of the neutron and X-ray powder diffraction techniques. The deuteride containing ∼1.8 deuterium atoms per alloy atom forms a titanium δ-hydride type of structure with deuterium atoms in the tetrahedral interstitial sites. The line broadening analysis of the deuteride phase suggests that the deuterization of the alloy causes strong lattice deformation effects, and the micro-strain is likely to be dislocation induced. In comparison with the deformation of the host Ti-Mo alloy matrix lattice, a relaxation effect is observed for the deformation of the interstitial deuterium sublattice

  2. A tangent formula derived from Patterson-function arguments. Pt. 3. Structure determination of zeolitic and layered materials from low-resolution powder diffraction data

    International Nuclear Information System (INIS)

    Rius, J.; Sane, J.; Miravitlles, C.; Gies, H.; Marler, B.; Oberhagemann, U.

    1995-01-01

    The viability of solving the structure type of zeolitic and layered materials applying multisolution direct methods to low-resolution (∼2.2 A) powder diffraction data is shown. The phases are refined with the tangent formula derived from Patterson-function arguments and the correct phase sets are discriminated with the conventional figures of merit. The two test examples presented are (a) the already known tetragonal zeolite ZSM-11 (space group I anti 4m2) at 2.3 A resolution and (b) the hitherto unknown layer silicate RUB-15 (Ibam) at 2.2 A resolution. In both cases, the tetrahedral Si units appear as resolved peaks in the Fourier maps computed with the phases of the highest-ranked direct-methods solutions. (orig.)

  3. Hydrogen molecule binding to unsaturated metal sites in metal-organic frameworks studied by neutron powder diffraction and inelastic neutron scattering

    Science.gov (United States)

    Liu, Yun; Brown, Craig; Neumann, Dan; Dinca, Mircea; Long, Jeffrey; Peterson, Vanessa; Kepert, Cameron

    2007-03-01

    Metal organic framework (MOF) materials have shown considerable potential for hydrogen storage arising from very large surface areas. However, the low binding energy of hydrogen molecules limits its storage capability to very low temperatures (industrial applications. Using neutron powder diffraction (NPD), we have characterized the hydrogen adsorption sites in a selected series of MOF materials with exposed unsaturated metal ions. Direct binding between the unsaturated metal ions and hydrogen molecules is observed and responsible for the enhanced initial hydrogen adsorption enthalpy. The different metals centers in these MOFs show different binding strength and interaction distances between the hydrogen molecule and metal ions. The organic linker also affects the overall H2 binding strength. Inelastic neutron scattering spectra of H2 in these MOFs are also discussed.

  4. Functional biocompatible magnetite-cellulose nanocomposite fibrous networks: Characterization by fourier transformed infrared spectroscopy, X-ray powder diffraction and field emission scanning electron microscopy analysis

    Science.gov (United States)

    Habibi, Neda

    2015-02-01

    The preparation and characterization of functional biocompatible magnetite-cellulose nano-composite fibrous material is described. Magnetite-cellulose nano-composite was prepared by a combination of the solution-based formation of magnetic nano-particles and subsequent coating with amino celluloses. Characterization was accomplished using X-ray powder diffraction (XRD), fourier transformed infrared (FTIR) and field emission scanning electron microscopy (FESEM) analysis. The peaks of Fe3O4 in the XRD pattern of nanocomposite confirm existence of the nanoparticles in the amino cellulose matrix. Magnetite-cellulose particles exhibit an average diameter of roughly 33 nm as demonstrated by field emission scanning electron microscopy. Magnetite nanoparticles were irregular spheres dispersed in the cellulose matrix. The vibration corresponding to the Nsbnd CH3 functional group about 2850 cm-1 is assigned in the FTIR spectra. Functionalized magnetite-cellulose nano-composite polymers have a potential range of application as targeted drug delivery system in biomedical field.

  5. Study of properties of chemically modified samples of halloysite mineral with X-ray fluorescence and X-ray powder diffraction methods

    Science.gov (United States)

    Banaś, D.; Kubala-Kukuś, A.; Braziewicz, J.; Majewska, U.; Pajek, M.; Wudarczyk-Moćko, J.; Czech, K.; Garnuszek, M.; Słomkiewicz, P.; Szczepanik, B.

    2013-12-01

    Elemental and chemical composition of raw and activated samples of halloysite mineral using wavelength dispersive X-ray fluorescence (WDXRF), total reflection X-ray fluorescence (TXRF) and X-ray powder diffraction (XRPD) methods were determined. As the result, it has been shown that application of the complementary X-ray spectrometry techniques allows very precise observation of changes in composition of halloysite mineral samples caused by its chemical modifications. Sample preparation procedure and usability of the research methods applied are described in details. Procedure of activation of raw halloysite mineral samples by etching them in sulfuric acid of various concentrations has been described and discussed. The ability of the samples to adsorb lead from intentionally contaminated water was tested and confirmed.

  6. In situ x-ray and neutron powder diffraction study of LaNi5-xSnx-H systems

    Science.gov (United States)

    Bowman, Robert C., Jr.; Nakamara, Yumiko; Akiba, Etsuo

    2004-01-01

    This paper will present results of in situ XRD measurements of LaNi4.75Sn0.25 .during the initial absorption-desorption cycle, These measurements were performed under a similar condition to that for LaNi4.75Al0.25 previously reported [1]. The data were analyzed by the Rietveld method. Lattice parameter change and strain formation accompanying hydride phase formation and decomposition will be discussed. In addition, results of in situ neutron diffraction of LaNi4.78Sn0.22, focusing on hydrogen occupation in the hydride phase, will be presented.

  7. New routes to synthesizing an ordered perovskite CaCu3Fe2Sb2O12 and its magnetic structure by neutron powder diffraction.

    Science.gov (United States)

    Larregola, Sebastian A; Zhou, Jianshi; Alonso, Jose A; Pomjakushin, Vladimir; Goodenough, John B

    2014-05-05

    The search for new double-perovskite oxides has grown rapidly in recent years because of their interesting physical properties like ferroelectricity, magnetism, and multiferroics. The synthesis of double perovskites, especially the A-site-ordered perovskites, in most cases needs to be made under high pressure, which is a drawback for applying these materials. Here we have demonstrated synthetic routes at ambient pressure by which we have obtained a high-quality duo-sites-ordered double perovskite, CaCu3Fe2Sb2O12, which has been previously synthesized under high pressure. The availability of a large quantity of the powder sample allows us to determine the crystal and magnetic structures by neutron powder diffraction (NPD) at 300 and 1.3 K. Measurements of the magnetization and heat capacity showed a ferrimagnetic transition at 160 K. A ferrimagnetic structure consisting of the uncompensated antiferromagnetic coupling between neighboring collinear copper and iron spins has been resolved from the low-temperature NPD data.

  8. Dehydrogenation kinetics of pure and nickel-doped magnesium hydride investigated by in situ time-resolved powder X-ray diffraction

    DEFF Research Database (Denmark)

    Jensen, T.R.; Andreasen, A.; Vegge, Tejs

    2006-01-01

    The dehydrogenation kinetics of pure and nickel (Ni)-doped (2w/w%) magnesium hydride (MgH2) have been investigated by in situ time-resolved powder X-ray diffraction (PXD). Deactivated samples, i.e. air exposed, are investigated in order to focus on the effect of magnesium oxide (MgO) surface layers......, which might be unavoidable for magnesium (Mg)-based storage media for mobile applications. A curved position-sensitive detector covering 120 degrees in 20 and a rotating anode X-ray source provide a time resolution of 45 s and up to 90 powder pattems collected during an experiment under isothermal...... by the Johnson-Mehi-Avrami formalism in order to derive rate constants at different temperatures. The apparent activation energies for dehydrogenation of pure and Ni-doped magnesium hydride were E-A approximate to 300 and 250 kJ/mol, respectively. Differential scanning calorimetry gave, E-A = 270 k...

  9. Characterization Studies of Cyclotron CS-30 Carbon Puller Material Using Powder X-Ray Diffraction and SEM, EDX Cross Section Method

    Science.gov (United States)

    Febriana, S.; Riyanto, E. S.; Dimyati, A.; Handayani, A.

    2018-01-01

    The carbon puller material of Cyclotron CS-30 has been characterized to investigate the structure and composition of the puller. Two samples of pullers have been prepared in the form of powder from locally made carbon and the original cyclotron puller. X-ray diffraction (XRD) analysis of both samples powder gives identification of the structure and phase type of carbon, meanwhile the morphology and the elemental composition of both samples can be shown by Scanning Electron Microscopy (SEM) and Energy Dispersive X-Ray Analysis (EDX) technique. XRD samples are prepared by grinding the puller surface meanwhile the samples for SEM analysis are prepared by cross section method. XRD result shows amorphous carbon structure and a typical broad XRD profile’s peaks and the diffused nature of the XRD profile indicate the presence of disorder in the samples. The first peak of the profile corresponds to the (002) peak of the hexagonal graphite structure, while the second peak corresponds to the (100) and (101) for both samples. Results of SEM-EDX showed that the carbon material from the original default puller of the CS-30 cyclotron contains mass percentage of lead significantly by 9.15%.

  10. X-ray and neutron powder diffraction studies of Ba(NdxY2-x)CuO5

    International Nuclear Information System (INIS)

    Liu, G.; Huang, Q.; Kaduk, J.A.; Yang, Z.; Lucas, C.; Wong-Ng, W.

    2008-01-01

    Ba(R,R') 2 CuO 5 (R,R'=lanthanides and Y) plays an important role as a flux-pinning agent in enhancing the superconducting properties of the Ba 2 (R,R')Cu 3 O 6+x (R,R'=lanthanides and Y) coated conductors. Using X-ray diffraction and neutron diffraction, we found that the Ba(Nd x Y 2-x )CuO 5 solid solution adopts two structure types. In the Nd-rich region (1.8≤x≤2.0), the materials are of brown color (commonly referred to as the 'brown phase'), and the structure is tetragonal with space group I4/mbm (no. 127). In the Y-rich region (0.0≤x≤1.4), the materials are green (commonly referred to as the 'green phase') and the structure is orthorhombic with space group Pnma (no. 62). A two-phase region (1.4 x Y 2-x )CuO 5 (isostructural to BaY 2 CuO 5 ), are discussed in this paper. - Graphical abstract: Perspective view of the 'green phase' Ba(Nd x Y 2-x )CuO 5 structure along the b-axis, showing the isolated square pyramids of [CuO 5 ] and the trigonal prisms, RO 7 , around the lanthanide sites

  11. Problems in determining the structure of the gamma brass alloy Cu64.8AL28.3Zn6.9 by powder and single crystal neutron diffraction

    International Nuclear Information System (INIS)

    Kisi, E.H.

    1988-01-01

    The structure of Cu 64.8 Al 28.3 Zn 6.9 , a ternary gamma brass derived from Cu 9 Al 4 by isomorphic substitution of Zn for Cu and Al atoms was investigated by Rietveld analysis of powder X-ray and neutron data and single crystal neutron diffraction. Structural differences arising from the two methods are contrasted, with reasons presented for favouring that from the powder refinements. A brief assessment of some problems associated with the solution of intermetallic structures is presented, highlighting the attractiveness of the powder method for this type of work. (author) 13 refs., 3 tabs

  12. Magnetic interactions in HoCr{sub 1-x}Fe{sub x}O{sub 3} (x = 0, 0.2) investigated by neutron powder diffraction

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Xinzhi, E-mail: liuxinzhi1984.cn@163.com [Department of Nuclear Physics, China Institute of Atomic Energy, Beijing 102413 (China); Hao, Lijie; Ma, Xiaobai [Department of Nuclear Physics, China Institute of Atomic Energy, Beijing 102413 (China); Wang, Chin-Wei [Neutron Group, National Synchrotron Radiation Research Center, Hsinchu 30077, Taiwan (China); Klose, Frank [Australian Nuclear Science and Technology Organization, Lucas Heights, New South Wales 2234 (Australia); Department of Physics and Materials Science, The City University of Hong Kong, Hong Kong Special Administrative Region (Hong Kong); Liu, Yuntao, E-mail: ytliu@ciae.ac.cn [Department of Nuclear Physics, China Institute of Atomic Energy, Beijing 102413 (China); Sun, Kai; Li, Yuqing [Department of Nuclear Physics, China Institute of Atomic Energy, Beijing 102413 (China); Chen, Dongfeng, E-mail: dongfeng@ciae.ac.cn [Department of Nuclear Physics, China Institute of Atomic Energy, Beijing 102413 (China)

    2017-07-01

    Highlights: • The temperature dependent magnetism of HoCr{sub 1-x}Fe{sub x}O{sub 3} (x = 0, 0.2) were investigated by neutron diffraction. • Cr{sup 3+} moment follows a mean field theory while Ho{sup 3+} follows a spin 1/2 model. • An magneto-elastic strain was observed accompanying with the ordering of Cr{sup 3+}. - Abstract: The temperature dependent magnetism of Fe-doped rare earth orthochromite HoCr{sub 1-x}Fe{sub x}O{sub 3}(x = 0, 0.2) was investigated by neutron powder diffraction. It is found that the magnetism of Cr(Fe){sup 3+} can be well understood within mean field theory, while the ordering of Ho{sup 3+} was induced by the Cr(Fe){sup 3+} sublattice and can be satisfyingly described by an effective S = 1/2 model. The absences of both the most common G{sub x}F{sub z} configuration of Cr{sup 3+} and the ordering of Ho{sup 3+} caused by Ho-Ho interaction evidence a strong Ho{sup 3+}-Cr{sup 3+} interaction which dominates this system. On the other hand, a remarkable magnetoelastic strain was observed accompanying the Cr(Fe){sup 3+} ordering. An analysis based on the equation of state with a Grüneisen approximation was performed and revealed magnetic origin of this strain.

  13. Crystal structure relation between tetragonal and orthorhombic CsAlD{sub 4}: DFT and time-of-flight neutron powder diffraction studies

    Energy Technology Data Exchange (ETDEWEB)

    Bernert, Thomas; Krech, Daniel; Felderhoff, Michael; Weidenthaler, Claudia [Department of Heterogeneous Catalysis, Max-Planck-Institut fuer Kohlenforschung, Muelheim/Ruhr (Germany); Kockelmann, Winfried [Rutherford Appleton Laboratory, Harwell Oxford, Didcot (United Kingdom); Frankcombe, Terry J. [Research School of Chemistry, The Australian National University, Canberra, ACT (Australia); School of Physical, Environmental and Mathematic Sciences, The University of New South Wales, Canberra, ACT (Australia)

    2015-11-15

    The crystal structures of orthorhombic and tetragonal CsAlD{sub 4} were refined from time-of-flight neutron powder diffraction data starting from atomic positions predicted from DFT calculations. The earlier proposed crystal structure of orthorhombic CsAlH{sub 4} is confirmed. For tetragonal CsAlH{sub 4}, DFT calculations predicted a crystal structure in I4{sub 1}/amd as potential minimum structure, while from neutron diffraction studies of CsAlD{sub 4} best refinement is obtained for a disordered structure in the space group I4{sub 1}/a, with a = 5.67231(9) Aa, c = 14.2823(5) Aa. While the caesium atoms are located on the Wyckoff position 4b and aluminium at Wyckoff position 4a, there are two distinct deuterium positions at the Wyckoff position 16f with occupancies of 50 % each. From this structure, the previously reported phase transition between the orthorhombic and tetragonal polymorphs could be explained. (Copyright copyright 2015 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  14. Evaluation via multivariate techniques of scale factor variability in the rietveld method applied to quantitative phase analysis with X ray powder diffraction

    Directory of Open Access Journals (Sweden)

    Terezinha Ferreira de Oliveira

    2006-12-01

    Full Text Available The present work uses multivariate statistical analysis as a form of establishing the main sources of error in the Quantitative Phase Analysis (QPA using the Rietveld method. The quantitative determination of crystalline phases using x ray powder diffraction is a complex measurement process whose results are influenced by several factors. Ternary mixtures of Al2O3, MgO and NiO were prepared under controlled conditions and the diffractions were obtained using the Bragg-Brentano geometric arrangement. It was possible to establish four sources of critical variations: the experimental absorption and the scale factor of NiO, which is the phase with the greatest linear absorption coefficient of the ternary mixture; the instrumental characteristics represented by mechanical errors of the goniometer and sample displacement; the other two phases (Al2O3 and MgO; and the temperature and relative humidity of the air in the laboratory. The error sources excessively impair the QPA with the Rietveld method. Therefore it becomes necessary to control them during the measurement procedure.

  15. Neutron powder diffraction study of the crystal and magnetic structures of BiNiO 3 at low temperature

    Science.gov (United States)

    Carlsson, Sandra J. E.; Azuma, Masaki; Shimakawa, Yuichi; Takano, Mikio; Hewat, Alan; Attfield, J. Paul

    2008-03-01

    The crystal and magnetic structures of the charge ordered perovskite BiNiO 3 have been studied at temperatures from 5 to 300 K using neutron diffraction. Rietveld analysis of the data shows that the structure remains triclinic (space group P1¯) throughout the whole temperature range. Bond-valence sum calculations based on the Bi-O and Ni-O bond distances confirm that the charge distribution is Bi 3+0.5Bi 5+0.5Ni 2+O 3 down to 5 K. The magnetic cell is identical to that of the triclinic superstructure and a G-type antiferromagnetic model gives a good fit to the magnetic intensities, with an ordered Ni 2+ moment of 1.76(3) μB at 5 K. However, BiNiO 3 is ferrimagnetic due to the inexact cancellation of opposing, inequivalent moments in the low symmetry cell.

  16. Neutron diffraction

    International Nuclear Information System (INIS)

    Bacon, G.E.

    1983-01-01

    The paper reviews neutron diffraction work from the early studies to the present-day development of the subject. Direct structural investigations were described, including chemical applications associated with single crystal techniques, and magnetic applications identified with powder techniques. The properties of the neutron beams are discussed, as well as the use of polarised beams. (UK)

  17. Synchrotron radiation

    CERN Document Server

    Kunz, C

    1974-01-01

    The production of synchrotron radiation as a by-product of circular high-energy electron (positron) accelerators or storage rings is briefly discussed. A listing of existing or planned synchrotron radiation laboratories is included. The following properties are discussed: spectrum, collimation, polarization, and intensity; a short comparison with other sources (lasers and X-ray tubes) is also given. The remainder of the paper describes the experimental installations at the Deutsches Elektronen-Synchrotron (DESY) and DORIS storage rings, presents a few typical examples out of the fields of atomic, molecular, and solid-state spectroscopy, and finishes with an outlook on the use of synchrotron radiation in molecular biology. (21 refs).

  18. In-situ synchrotron diffraction and digital image correlation technique for characterizations of retained austenite stability in low-alloyed transformation induced plasticity steel

    International Nuclear Information System (INIS)

    Brauser, S.; Kromm, A.; Kannengiesser, Th.; Rethmeier, M.

    2010-01-01

    Direct measurement and quantification of phase transformation in a low-alloyed transformation induced plasticity steels depending on the tensile load as well as determination of the real true stress and true strain values were carried out in-situ using high energy synchrotron radiation. Digital image correlation technique was used to quantify more precisely the true strain values. The aim of the work was to obtain a better understanding of the phase transformation of commercial low-alloyed transformation induced plasticity steel depending on the true strain and true stress values.

  19. A multiple CCD X-ray detector and its first operation with synchrotron radiation X-ray beam

    International Nuclear Information System (INIS)

    Suzuki, Masayo; Yamamoto, Masaki; Kumasaka, Takashi; Sato, Kazumichi; Toyokawa, Hidenori; Aries, Ian F.; Jerram, Paul A.; Ueki, Tatzuo

    1999-01-01

    A 4x4 array structure of 16 identical CCD X-ray detector modules, called the multiple CCD X-ray detector system (MCCDX), was submitted to its first synchrotron radiation experiment at the protein crystallography station of the RIKEN beamline (BL45XU) at the SPring-8 facility. An X-ray diffraction pattern of cholesterol powder was specifically taken in order to investigate the overall system performance

  20. A multiple CCD X-ray detector and its first operation with synchrotron radiation X-ray beam

    CERN Document Server

    Suzuki, M; Kumasaka, T; Sato, K; Toyokawa, H; Aries, I F; Jerram, P A; Ueki, T

    1999-01-01

    A 4x4 array structure of 16 identical CCD X-ray detector modules, called the multiple CCD X-ray detector system (MCCDX), was submitted to its first synchrotron radiation experiment at the protein crystallography station of the RIKEN beamline (BL45XU) at the SPring-8 facility. An X-ray diffraction pattern of cholesterol powder was specifically taken in order to investigate the overall system performance.

  1. In situ defect annealing of swift heavy ion irradiated CeO2 and ThO2 using synchrotron X-ray diffraction and a hydrothermal diamond anvil cell

    Energy Technology Data Exchange (ETDEWEB)

    Palomares, Raul I.; Tracy, Cameron L.; Zhang, Fuxiang; Park, Changyong; Popov, Dmitry; Trautmann, Christina; Ewing, Rodney C.; Lang, Maik

    2015-04-16

    Hydrothermal diamond anvil cells (HDACs) provide facile means for coupling synchrotron X-ray techniques with pressure up to 10 GPa and temperature up to 1300 K. This manuscript reports on an application of the HDAC as an ambient-pressure sample environment for performingin situdefect annealing and thermal expansion studies of swift heavy ion irradiated CeO2and ThO2using synchrotron X-ray diffraction. The advantages of thein situHDAC technique over conventional annealing methods include rapid temperature ramping and quench times, high-resolution measurement capability, simultaneous annealing of multiple samples, and prolonged temperature and apparatus stability at high temperatures. Isochronal annealing between 300 and 1100 K revealed two-stage and one-stage defect recovery processes for irradiated CeO2and ThO2, respectively, indicating that the morphology of the defects produced by swift heavy ion irradiation of these two materials differs significantly. These results suggest that electronic configuration plays a major role in both the radiation-induced defect production and high-temperature defect recovery mechanisms of CeO2and ThO2.

  2. Investigation of the Microstructure Evolution in a Fe-17Mn-1.5Al-0.3C Steel via In Situ Synchrotron X-ray Diffraction during a Tensile Test

    Directory of Open Access Journals (Sweden)

    Yan Ma

    2017-09-01

    Full Text Available The quantitative characterization of the microstructure evolution in high-Mn steel during deformation is of great importance to understanding its strain-hardening behavior. In the current study, in situ high-energy synchrotron X-ray diffraction was employed to characterize the microstructure evolution in a Fe-17Mn-1.5Al-0.3C steel during a tensile test. The microstructure at different engineering strain levels—in terms of ε-martensite and α’-martensite volume fractions, the stacking fault probability, and the twin fault probability—was analyzed by the Rietveld refinement method. The Fe-17Mn-1.5Al-0.3C steel exhibits a high ultimate tensile strength with a superior uniform elongation and a high strain-hardening rate. The remaining high strain-hardening rate at the strain level about 0.025 to 0.35 results from ε-martensite dominant transformation-induced-plasticity (TRIP effect. The increase in the strain-hardening rate at the strain level around 0.35 to 0.43 is attributed to the synergetic α’-martensite dominant TRIP and twinning-induced-plasticity (TWIP effects. An evaluation of the stacking fault energy (SFE of the Fe-17Mn-1.5Al-0.3C steel by the synchrotron measurements shows good agreement with the thermodynamic calculation of the SFE.

  3. Investigation of the Microstructure Evolution in a Fe-17Mn-1.5Al-0.3C Steel via In Situ Synchrotron X-ray Diffraction during a Tensile Test.

    Science.gov (United States)

    Ma, Yan; Song, Wenwen; Bleck, Wolfgang

    2017-09-25

    The quantitative characterization of the microstructure evolution in high-Mn steel during deformation is of great importance to understanding its strain-hardening behavior. In the current study, in situ high-energy synchrotron X-ray diffraction was employed to characterize the microstructure evolution in a Fe-17Mn-1.5Al-0.3C steel during a tensile test. The microstructure at different engineering strain levels-in terms of ε-martensite and α'-martensite volume fractions, the stacking fault probability, and the twin fault probability-was analyzed by the Rietveld refinement method. The Fe-17Mn-1.5Al-0.3C steel exhibits a high ultimate tensile strength with a superior uniform elongation and a high strain-hardening rate. The remaining high strain-hardening rate at the strain level about 0.025 to 0.35 results from ε-martensite dominant transformation-induced-plasticity (TRIP) effect. The increase in the strain-hardening rate at the strain level around 0.35 to 0.43 is attributed to the synergetic α'-martensite dominant TRIP and twinning-induced-plasticity (TWIP) effects. An evaluation of the stacking fault energy (SFE) of the Fe-17Mn-1.5Al-0.3C steel by the synchrotron measurements shows good agreement with the thermodynamic calculation of the SFE.

  4. Time-resolved x-ray diffraction studies on the intensity changes of the 5.9 and 5.1 nm actin layer lines from frog skeletal muscle during an isometric tetanus using synchrotron radiation

    International Nuclear Information System (INIS)

    Wakabayashi, K.; Tanaka, H.; Amemiya, Y.; Fujishima, A.; Kobayashi, T.; Hamanaka, T.; Sugi, H.; Mitsui, T.

    1985-01-01

    Time-resolved x-ray diffraction studies have been made on the 5.9- and 5.1-nm actin layer lines from frog skeletal muscles during an isometric tetanus at 6 degrees C, using synchrotron radiation. The integrated intensities of these actin layer lines were found to increase during a tetanus by 30-50% for the 5.9-nm reflection and approximately 70% for the 5.1-nm reflection of the resting values. The intensity increase of both reflections was greater than that taking place in the transition from rest to rigor state. The intensity change of the 5.9-nm reflection preceded those of the myosin 42.9-nm off-meridional reflection and of the equatorial reflections, as well as the isometric tension development. The intensity profile of the 5.9-nm layer line during contraction was found to be different from that observed in the rigor state

  5. Synchrotron radiation

    International Nuclear Information System (INIS)

    Nave, C.; Quinn, P.; Blake, R.J.

    1988-01-01

    The paper on Synchrotron Radiation contains the appendix to the Daresbury Annual Report 1987/88. The appendix is mainly devoted to the scientific progress reports on the work at the Synchrotron Radiation Source in 1987/8. The parameters of the Experimental Stations and the index to the Scientific Reports are also included in the appendix. (U.K.)

  6. Australian synchrotron radiation science

    International Nuclear Information System (INIS)

    White, J.W.

    1996-01-01

    Full text: The Australian Synchrotron Radiation Program, ASRP, has been set up as a major national research facility to provide facilities for scientists and technologists in physics, chemistry, biology and materials science who need access to synchrotron radiation. Australia has a strong tradition in crystallography and structure determination covering small molecule crystallography, biological and protein crystallography, diffraction science and materials science and several strong groups are working in x-ray optics, soft x-ray and vacuum ultra-violet physics. A number of groups whose primary interest is in the structure and dynamics of surfaces, catalysts, polymer and surfactant science and colloid science are hoping to use scattering methods and, if experience in Europe, Japan and USA can be taken as a guide, many of these groups will need third generation synchrotron access. To provide for this growing community, the Australian National Beamline at the Photon Factory, Tsukuba, Japan, has been established since 1990 through a generous collaboration with Japanese colleagues, the beamline equipment being largely produced in Australia. This will be supplemented in 1997 with access to the world's most powerful synchrotron x-ray source at the Advanced Photon Source, Argonne National Laboratory, USA. Some recent experiments in surface science using neutrons as well as x-rays from the Australian National Beamline will be used to illustrate one of the challenges that synchrotron x-rays may meet

  7. Structure determination of enalapril maleate form II from high-resolution X-ray powder diffraction data.

    Science.gov (United States)

    Kiang, Y-H; Huq, Ashfia; Stephens, Peter W; Xu, Wei

    2003-09-01

    The crystal structure of polymorphic Form II of enalapril maleate, a potent angiotensin-converting enzyme inhibitor, was determined from high-resolution X-ray diffraction data using the direct space method. Enalapril maleate Form II crystallizes in space group P2(1)2(1)2(1), Z = 4, with unit cell parameters a = 33.9898(3) A, b = 11.2109(1) A, c = 6.64195(7) A, and V = 2530.96(5) A(3). By treating the molecules as rigid bodies and using the bond lengths and angles obtained from the X-ray single crystal structures of Form I, which were solved almost 20 years ago, the total degrees of freedom of enalapril maleate were reduced from 25 to 12. This reduction in total degrees of freedom allowed the simulated annealing to complete within a reasonable computation time. In the crystal structure of Form II, the crystal packing, hydrogen-bonding pattern, and conformation of enalapril maleate resemble those in the structure of Form I. The crystal packing and conformation of enalapril maleate in the two polymorphic forms may explain the similarity of the thermal properties, (13)C nuclear magnetic resonance, Fourier transform infrared, and Raman spectra of Forms I and II. In both structures, the conformations of the main peptide chains, which are considered responsible for binding the active angiotensin-converting enzyme sites, remain largely unchanged. Lattice energy calculation showed that Form II is slightly more stable than Form I by 3.5 kcal/mole. Copyright 2003 Wiley-Liss, Inc. and the American Pharmacists Association

  8. Optimised Combined Angular and Energy Dispersive Diffraction at the PSICHE Beam Line of the SOLEIL Synchrotron for Fast, High Q-range Structure Determination at High Pressure and Temperature.

    Science.gov (United States)

    King, A.; Guignot, N.; Boulard, E.; Deslandes, J. P.; Clark, A. N.; Morard, G.; Itié, J. P.

    2017-12-01

    Synchrotron diffraction is an ideal technique for investigating materials at high pressure and temperature, because the penetrating nature of high-energy X-rays allows measurements to be made inside pressure cells or sample environments. Wang et al. described the CAESAR acquisition strategy, in which energy and angular dispersive techniques are combined to produce an instrument particularly suitable for quantitative measurements from samples inside high-pressure apparati [1]. The PSICHE beam line of the SOLEIL Synchrotron is equipped with such a CAESAR system. Uniquely, this system allows energy dispersive diffraction spectra to be acquired at scattering angles between -5 and +30 degrees two theta, while maintaining a sphere of confusion at the measurement position in the order of 10 microns. The slits used to define the scattering angle act as Soller slits and select the diffracted volume, separating the sample from its environment. By developing an optimised acquisition strategy we are able to obtain data covering a very wide Q range (to 160nm-1 or more), while minimising the total acquisition time (one hour per complete acquisition). In addition, the 2D nature (angle and energy) of the acquired dataset enables the effective incident spectrum to be efficiently determined with no addition measurements, in order to normalise the acquired data. The resulting profile of scattered intensity as a function of Q is suitable for Fourier transform analysis of liquid or amorphous structures. PSICHE is a multi technique beam line, with a part of the beam time dedicated to parallel beam absorption and phase contrast radiography and tomography [2]. Examples will be given to show how these techniques can be combined with diffraction techniques to greatly enrich studies of materials at extreme conditions. [1] Wang, Y., Uchida, T., Von Dreele, R., Rivers, M. L., Nishiyama, N., Funakoshi, K., Nozawa, A., and Keneko, H., J. Appl. Crystallogr. 37, 947 (2004). [2] King, A., Guignot

  9. Study of the magnetic and electronic properties of nanocrystalline PrCo3 by neutron powder diffraction and density functional theory.

    Science.gov (United States)

    Younsi, Khedidja; Crivello, Jean-Claude; Paul-Boncour, Valérie; Bessais, Lotfi; Porcher, Florence; André, Gilles

    2013-03-20

    Nanocrystalline PrCo(3) powder has been synthesized by high-energy milling and was subsequently annealed from 873 to 1273 K for 30 min to optimize the extrinsic properties. The structure and magnetic properties of the nanocrystalline PrCo(3) have been investigated by means of x-ray and neutron diffraction as well as magnetization measurements. All compounds crystallize in the same PuNi(3) type structure, with grain sizes between 28 and 47 nm. As the annealing temperature increases, a maximum coercive field of 12 kOe at 300 K (55 kOe at 10 K) was obtained by annealing at 1023 K for a grain size of 35 nm. The refinement of the neutron powder diffraction patterns (NPD) of PrCo(3) from 1.8 to 300 K shows an expansion of the parameter a and a contraction of the parameter c, leading to a decrease of the ratio c/a. The evolution of the Co and Pr magnetic sublattices measured by NPD indicates that this compound is a highly anisotropic uniaxial ferromagnet with the easy magnetization axis parallel to c(-->). This experimental study has been completed by a theoretical investigation of the electronic structure of the PrCo(x) (x = 2, 3 and 5) compounds. Band structure calculations with collinear spin polarization were performed by using the local approximation of the density functional theory scheme implemented in the projector-augmented wave method. The electronic structure of PrCo(3) compound in both directions of spin shows that the majority of occupied states are dominated by the 3d states of Co, with a strong electronic charge transfer from Pr to Co. The PrCo(3) electronic structure can be explained by a superimposition of those of PrCo(2) and PrCo(5), as expected from its crystal structure. The magnetic anisotropy has been confirmed for PrCo(3), as a non-collinear spin calculation with the polarization along the c axis is shown to be more stable than with the polarization in the (a(-->),b(-->)) plane.

  10. Sample cell for in-field X-ray diffraction experiments

    Directory of Open Access Journals (Sweden)

    Viktor Höglin

    2015-01-01

    Full Text Available A sample cell making it possible to perform synchrotron radiation X-ray powder diffraction experiments in a magnetic field of 0.35 T has been constructed. The device is an add-on to an existing sample cell and contains a strong permanent magnet of NdFeB-type. Experiments have shown that the setup is working satisfactory making it possible to perform in-field measurements.

  11. (Nd/Pr)2NiO4+δ: Reaction Intermediates and Redox Behavior Explored by in Situ Neutron Powder Diffraction during Electrochemical Oxygen Intercalation.

    Science.gov (United States)

    Ceretti, Monica; Wahyudi, Olivia; André, Gilles; Meven, Martin; Villesuzanne, Antoine; Paulus, Werner

    2018-04-16

    Oxygen intercalation/deintercalation in Pr 2 NiO 4+δ and Nd 2 NiO 4+δ was followed by in situ neutron powder diffraction during electrochemical oxidation/reduction, in a dedicated reaction cell at room temperature. For both systems three phases, all showing the same line width, were identified. The starting phases Pr 2 NiO 4.23 and Nd 2 NiO 4.24 , considered with an average orthorhombic Fmmm symmetry, although both show a slight monoclinic distortion, get reduced in a two-phase reaction step to tetragonal intermediate phases with 0.07 ≤ δ ≤ 0.10 and P4 2 / ncm space group, which on further reduction transform, again in a two-phase reaction step, toward the respective stoichiometric (Pr/Nd) 2 NiO 4.0 phases, with Bmab space group. Electrochemical oxidation does, however, not proceed fully reversibly for both cases: while the reoxidation of Nd 2 NiO 4+δ is limited to the tetragonal intermediate phase with δ = 0.10, the homologous Pr 2 NiO 4+δ can be reoxidized up to δ = 0.17, showing orthorhombic symmetry. For the intermediate tetragonal phase, we were able to establish for Pr 2 NiO 4.09 a complex anharmonic displacement behavior of the apical oxygen atoms, as analyzed by single-crystal neutron diffraction and maximum entropy analysis, in agreement with a low- T diffusion pathway for oxygen ions, activated by lattice dynamics.

  12. Advances in martensitic transformations in Cu-based shape memory alloys achieved by in situ neutron and synchrotron X-ray diffraction methods

    OpenAIRE

    MALARD , Benoît; Sittner , Petr; Berveiller , Sophie; Patoor , Etienne

    2012-01-01

    International audience; This article deals with the application of several X-ray and neutron diffraction methods to investigate the mechanics of a stress induced martensitic transformation in Cu-based shape memory alloy polycrystals. It puts experimental results obtained by two different research groups on different length scales into context with the mechanics of stress induced martensitic transformation in polycrystalline environment.

  13. Poly[μ-(1-azaniumylethane-1,1-diyl)- bis(hydrogen phosphonato)sodium]: A powder X-ray diffraction study

    International Nuclear Information System (INIS)

    Rukiah, M.; Assaad, T.

    2015-01-01

    The title two-dimensional coordination polymer, [Na(C2H8NO6P2)]n, was characterized using powder X-ray diffraction data and its structure refined using the Rietveld method. The asymmetric unit contains one Na(+) cation and one (1-azaniumylethane-1,1-diyl)bis(hydrogen phosphonate) anion. The central Na(+) cation exhibits distorted octahedral coordination geometry involving two deprotonated O atoms, two hydroxy O atoms and two double-bonded O atoms of the bisphosphonate anion. Pairs of sodium-centred octahedra share edges and the pairs are in turn connected to each other by the biphosphonate anion to form a two-dimensional network parallel to the (001) plane. The polymeric layers are connected by strong O-H...O hydrogen bonding between the hydroxy group and one of the free O atoms of the bisphosphonate anion to generate a three-dimensional network. Further stabilization of the crystal structure is achived by N-H...O and O-H...O hydrogen bonding.(author)

  14. Crystal structure refinement of the ternary compound Cu{sub 2}SnTe{sub 3} by X-ray powder diffraction

    Energy Technology Data Exchange (ETDEWEB)

    Mora, A.J. [Laboratorio de Cristalografia, Departamento de Quimica, Facultad de Ciencias, Universidad de Los Andes, Merida (Venezuela); Marcano, G.; Rincon, C. [Centro de Estudios de Semiconductores, Departamento de Fisica, Facultad de Ciencias, Universidad de Los Andes, Merida (Venezuela); Delgado, G.E.

    2008-04-15

    The ternary compound Cu{sub 2}SnTe{sub 3} crystallizes in the Imm2 (N circle 44) space group, Z=2, with a=2.833(4) A, b=4.274(1) A, c=6.043(1) A, V=331.5(1) A{sup 3}. Its structure was refined from X-ray powder diffraction data using the Rietveld method. The refinement of 25 instrumental and structural variables led to R{sub p}=10.2%, R{sub wp}=11.8%, R{sub exp}=7.7%, R{sub B}=10.6%, S=1.6 and {chi}{sup 2}=2.6, for 5501 step intensities and 163 independent reflections. This compound is isostructural with Cu{sub 2}GeSe{sub 3}, and consists of a three-dimensional arrangement of slightly distorted CuTe{sub 4} and SnTe{sub 4} tetrahedra connected by common corners. (copyright 2008 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

  15. Quantifying low amorphous or crystalline amounts of alpha-lactose-monohydrate using X-ray powder diffraction, near-infrared spectroscopy, and differential scanning calorimetry.

    Science.gov (United States)

    Fix, I; Steffens, K J

    2004-05-01

    Efficient and accurate quantification of low amorphous and crystalline contents within pharmaceutical materials still remains a challenging task in the pharmaceutical industry. Since X-ray powder diffraction (XRPD) equipment has improved in recent years, our aim was 1) to investigate the possibility of substantially lowering the detection limits of amorphous or crystalline material to about 1% or 0.5% w/w respectively by applying conventional Bragg Brentano optics, combined with a fast and simple evaluation technique; 2) to perform these measurements within a short time to make it suitable for routine analysis; and 3) to subject the same data sets to a partial least squares regression (PLSR) in order to investigate whether it is possible to improve accuracy and precision compared to the standard integration method. Near-infrared spectroscopy (NIRS) and differential scanning calorimetry (DSC) were chosen as reference method. As model substance, alpha lactose monohydrate was chosen to create calibration curves based on predetermined mixtures of highly crystalline and amorphous substance. In contrast to DSC, XRPD and NIRS revealed an excellent linearity, precision, and accuracy with the percent of crystalline amount and a detectability down to about 0.5% w/w. Chemometric evaluation (partial least squares regression) applied to the XRPD data further improved the quality of our calibration.

  16. Equation of state and phase transition of deuterated ammonia monohydrate (ND3.D2O) measured by high-resolution neutron powder diffraction up to 500 MPa.

    Science.gov (United States)

    Fortes, A Dominic; Suard, Emmanuelle; Lemée-Cailleau, Marie-Hélène; Pickard, Christopher J; Needs, Richard J

    2009-10-21

    We describe the results of a neutron powder diffraction study of perdeuterated ammonia monohydrate (AMH, ND(3).D(2)O) carried out in the range 102high-resolution diffractometer at the Institut Laue-Langevin. This paper reports observations of the phase transformation from the low-pressure P2(1)2(1)2(1) phase (AMH I) to the high-pressure Pbca phase (AMH II) at 351 MPa, and measurements which have allowed us to determine the volumetric and axial incompressibilities of both polymorphs. At 180 K, the fitted third order Birch-Murnaghan equation of state of AMH I has parameters, V(0)=248.00(2) A(3), K(0)=7.33(3) GPa with the first pressure derivative of K(0) fixed at the value obtained in ab initio calculations, (partial differentialK(0)/partial differentialP)(T)=K(0)'=5.3; the implied value of the second derivative is therefore (partial differential(2)K(0)/partial differentialP(2))(T)=K(0)"=-0.94(1) GPa(-1). At 351 MPa, we observed that the transition from AMH I to AMH II occurred over a period of 90 min, with an associated reduction in molar volume of 4.6% and an increase in the incompressibility of 19.6%.

  17. Shaft cryostat on the basis of a closed-circuit refrigerator for neutron powder diffraction studies in the temperature range 6-300 K

    International Nuclear Information System (INIS)

    Chernikov, A.N.; Zhuravlev, V.V.; Ul'yanov, V.A.; Trunov, V.A.; Bulkin, A.P.; Kolkhidashvili, M.R.

    2005-01-01

    A description of a cryostat on the basis of the closed cycle refrigerator CoolPower 5/100T for operation in the temperature range 6.2-300 K is presented. The cryostat is intended for a sample up to 18 mm in diameter and up to 100 mm of length. The reload of the sample placed into the ampoule, which is made of TiZr alloy, is performed at any temperature of the refrigerator with the help of an insert. Thermal connection between the sample and the heat exchanger of the refrigerator second step is performed with the help of heat exchange gas helium-4. The minimal temperature of the sample is 6.2 K at the accuracy of the temperature stabilization of the sample 0.1 K. Measurement and temperature stabilization is performed by a controller connected with a computer. Dependences of temperature measurements on time at cooling and heating are presented. The shaft cryostat was developed to carry out the experiments on neutron diffraction from powder samples

  18. Investigation by laser induced breakdown spectroscopy, X-ray fluorescence and X-ray powder diffraction of the chemical composition of white clay ceramic tiles from Veliki Preslav

    Energy Technology Data Exchange (ETDEWEB)

    Blagoev, K., E-mail: kblagoev@issp.bas.bg [Institute of Solid State Physics, Bulgarian Academy of Sciences, 72 Tzarigradsko Chaussee, 1784 Sofia (Bulgaria); Grozeva, M., E-mail: margo@issp.bas.bg [Institute of Solid State Physics, Bulgarian Academy of Sciences, 72 Tzarigradsko Chaussee, 1784 Sofia (Bulgaria); Malcheva, G., E-mail: bobcheva@issp.bas.bg [Institute of Solid State Physics, Bulgarian Academy of Sciences, 72 Tzarigradsko Chaussee, 1784 Sofia (Bulgaria); Neykova, S., E-mail: sevdalinaneikova@abv.bg [National Institute of Archaeology with Museum, Bulgarian Academy of Sciences, 2 Saborna, 1000 Sofia (Bulgaria)

    2013-01-01

    The paper presents the results of the application of laser induced breakdown spectroscopy, X-ray fluorescence spectrometry, and X-ray powder diffraction in assessing the chemical and phase composition of white clay decorative ceramic tiles from the medieval archaeological site of Veliki Preslav, a Bulgarian capital in the period 893–972 AC, well-known for its original ceramic production. Numerous white clay ceramic tiles with highly varied decoration, produced for wall decoration of city's churches and palaces, were found during the archaeological excavations in the old capital. The examination of fourteen ceramic tiles discovered in one of the city's monasteries is aimed at characterization of the chemical profile of the white-clay decorative ceramics produced in Veliki Preslav. Combining different methods and comparing the obtained results provides complementary information regarding the white-clay ceramic production in Veliki Preslav and complete chemical characterization of the examined artefacts. - Highlights: ► LIBS, XRF and XRD analyses of medieval white-clay ceramic tiles fragments are done. ► Different elements and phases, presented in the ceramics fragments were determined. ► Differences in the tiles' raw material mineral composition are found. ► Information of the tiles' production process and the raw clay deposits is obtained.

  19. Study of properties of chemically modified samples of halloysite mineral with X-ray fluorescence and X-ray powder diffraction methods

    International Nuclear Information System (INIS)

    Banaś, D.; Kubala-Kukuś, A.; Braziewicz, J.; Majewska, U.; Pajek, M.; Wudarczyk-Moćko, J.; Czech, K.; Garnuszek, M.; Słomkiewicz, P.; Szczepanik, B.

    2013-01-01

    Elemental and chemical composition of raw and activated samples of halloysite mineral using wavelength dispersive X-ray fluorescence (WDXRF), total reflection X-ray fluorescence (TXRF) and X-ray powder diffraction (XRPD) methods were determined. As the result, it has been shown that application of the complementary X-ray spectrometry techniques allows very precise observation of changes in composition of halloysite mineral samples caused by its chemical modifications. Sample preparation procedure and usability of the research methods applied are described in details. Procedure of activation of raw halloysite mineral samples by etching them in sulfuric acid of various concentrations has been described and discussed. The ability of the samples to adsorb lead from intentionally contaminated water was tested and confirmed. - Author-Highlights: • We measured elemental and chemical composition of raw and activated halloysite mineral samples. • We showed that X-ray techniques allow precise study of changes in the sample composition. • We describe procedure of activation of the samples by etching them in sulfuric acid. • We tested ability of halloysite mineral to absorb lead from contaminated water

  20. Magnetic and electronic properties of RNiO{sub 3} (R = Pr, Nd, Eu, Ho and Y) perovskites studied by resonant soft x-ray magnetic powder diffraction

    Energy Technology Data Exchange (ETDEWEB)

    Bodenthin, Y; Staub, U; Piamonteze, C; Garcia-Fernandez, M [Swiss Light Source, Paul Scherrer Institut, CH-5232 Villigen PSI (Switzerland); Martinez-Lope, M J; Alonso, J A, E-mail: urs.staub@psi.ch [Instituto de Ciencia de Materiales de Madrid, CSIC, Cantoblanco, E-28049 Madrid (Spain)

    2011-01-26

    Soft x-ray resonant magnetic powder diffraction of the (1/2 0 1/2) reflection at the Ni L{sub 2,3} edges is used to study the magnetic and electronic properties of a series of RNiO{sub 3} materials (with R = Pr, Nd, Eu, Ho and Y) below the metal-insulator transition. The polarization and energy dependence of the reflection gives further support for a non-collinear magnetic structure and charge disproportionation in the whole RNiO{sub 3} series. Only small changes in the spectra of the magnetic (1/2 0 1/2) reflection and in the absorption spectra could be detected. The results are discussed with comparison to charge transfer multiplet calculations. Our results emphasize that the lighter and heavier RNiO{sub 3} compounds are very similar from the point of view of their local electronic and magnetic state despite the strong change of the metal-to-insulator transition temperature.