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  • Wiley-Blackwell  (22,088)
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  • 1
    Electronic Resource
    Electronic Resource
    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 11 (1978), S. 73-79 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: In order to avoid some of the disadvantages associated with the desmearing methods, a procedure has been developed where the smeared, primary, intensity data can be evaluated directly without desmearing. The procedure consists of the following: first, a model depending on a vector of unknowns, x = (x1, ...., xn), is constructed; then, an iterative search is made for the vector x, and a scale factor s, which corresponds to a local minimum in the error square sum based on the primary, slit-smeared, intensity data. The main advantages with the present method are that the comparison between theory and experiment is made directly with the experimental quantity; thus the experimental errors can be considered in this comparison. Furthermore, some of the disadvantages associated with the desmearing methods are avoided; the method is numerically stable and no extrapolations outside the measured angular range are necessary. Several data sets measured at different concentrations and with different, completely arbitrary, primary-beam weighting functions can be considered in the same refinement. The interparticle scattering effect may also be included in the least-squares refinement. The method is general, so that different models can be tested simply by changing only one subroutine of the computer program. It may also be used to evaluate data impaired by other types of resolution errors; for example, effects due to polychromatic radiation or resolution errors in neutron scattering. Two constructed examples of the application of the method are given: (1) the calculation of the dimensions and the molecular weight of particles with a shape which can be approximated with an ellipsoid of revolution; (2) the calculation of the dimensions and electron-density distribution for spherical particles.
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  • 2
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 11 (1978), S. 114-120 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: A method is described for finding the peak limits of a Bragg reflection from an analysis of its profile. A `window' of ± 0.67σ[φ)(x)] is set up on each ordinate φ(x) in the tails of the profile and the pattern of the following ordinates is observed through the window. As the ordinate moves from the peak to the background the pattern changes and the limits of the peak may be recognized. Bragg reflections from three crystals have been analysed by this method and the limits found were generally wider than those determined by the method of Lehmann & Larsen [Acta Cryst. (1974), A30, 580–584] applied to the same data. The value of σ(I)/I was near the minimum and similar to the value from the corrected Lehmann–Larsen limits. The behaviour of the methods is also compared by representing the reflections by equivalent Gaussian profiles, and it is found that 〉99% of the Gaussian peak is within the limits found by the present method.
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  • 3
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 11 (1978), S. 102-113 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: Existing knowledge about Scherrer constants is reviewed and a summary is given of the interpretation of the broadening arising from small crystallites. Early work involving the half-width as a measure of breadth has been completed and Scherrer constants of simple regular shapes have been determined for all low-angle reflections (h2 + k2 + l2 ≤ 100) for four measures of breadth. The systematic variation of Scherrer constant with hkl is discussed and a convenient representation in the form of contour maps is applied to simple shapes. The relation between the `apparent' crystallite size, as determined by X-ray methods, and the `true' size is considered for crystallites having the same shape. If they are of the same size, then the normal Scherrer constant applies, but if there is a distribution of sizes, a modified Scherrer constant must be used.
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  • 4
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 11 (1978), S. 137-140 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: The resolution problem in X-ray energy-dispersive diffractometry is discussed. It is shown that for a given characteristic of the solid-state detector system and a given range of interplanar spacings, an optimum scattering angle can be easily found for any divergence of the incident and scattered beams.
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  • 5
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 11 (1978), S. 148-150 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: Spherical crystals of alloy phases too hard and brittle for grinding can be obtained by partial remelting and solidification of a powder sample. The alloy powder is blown through an argon-plasma jet melting the surface material of individual fragments, which solidify again as nearly perfect spheres. The yield is a mixture of different materials in which it is possible, however, after heat treatment to find good single crystals of the original composition. Spherical single crystals of Cu9Al4 have been produced by this method and used for a high-precision X-ray investigation described elsewhere.
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  • 6
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 11 (1978), S. 157-158 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: Completely transparent and colourless single crystals of PbGe3O7 were grown from a melt of composition PbO.2GeO2 at 1040 K by spontaneous crystallization. The compound melts incongruently at 1070 K. The unit cell is orthorhombic with lattice constants a = 5.270 (2), b = 14.088 (4), c = 16.054 (4) Å; D293 = 5.94 (4), Dx = 5.985 g cm−3 for Z = 8. The probable space group is Pcab (D152h). A reported phase of composition PbGe205 is shown to be a mixture of PbGe3O7 and α-PbGeO3. X-ray powder data are given.
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  • 7
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 11 (1978), S. 238-242 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: An X-ray diffraction study of CsDNA has been carried out with the use of synchrotron radiation of wavelength λ = 1.2 Å. The geometry corresponds to a cylindrical specimen brought into a cylindrical beam of the same diameter and the absorption factor and the primary-beam attenuation factor have been calculated as functions of specimen μR for this geometry. The optimum size of a specimen is here about 1.5 times greater than that in the case of a plane-parallel beam used in International Tables for X-ray Crystallography [Vol. II, (1967), 2nd ed., p. 295. Birmingham: Kynoch Press]. Experimental and calculated primary-beam attenuation factors have been compared and the experimental value of the linear absorption coefficient μ of CsDNA has been estimated for various humidities. The agreement between μc = 78.1 and μo = 78.2 ± 3.6 cm−1 (relative humidity 66–75%) indicates that the geometrical model used is suitable to describe polymer fibres in a cylindrical beam of nearly the same size. It is seen from the observed μ values that there is one caesium ion per nucleotide (monomer unit of DNA molecule) in the specimens used.
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  • 8
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 11 (1978), S. 293-294 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
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  • 9
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 11 (1978), S. 293-293 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
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  • 10
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 11 (1978), S. 294-294 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
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  • 11
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 11 (1978), S. 346-375 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: Recent advances in the small-angle scattering of X-rays, neutrons and light by polymers are reviewed. The three techniques are compared, from both experimental and theoretical points of view. Applications are discussed for the study of homophase and heterophase polymers, both in solution and in the solid state, as well as for unoriented and oriented crystalline polymers.
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  • 12
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 11 (1978), S. 477-477 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: The conformations of different IgG antibodies were studied before and after interaction with antigen (hapten). In every case a strong change of the conformation was observed. Binding of hapten caused a decrease of the radius of gyration by 2 to 8% and a decrease of the volume by 3 to 10%, depending on the degree of saturation with hapten. Two IgG antibodies (anti-poly-d-alanyl) were split by enzymes into fragments which contain one binding site (Fab′) and two binding sites (Fab′)2, respectively, for hapten. No changes of conformation were observed with these fragments upon the interaction with hapten. These findings lead to the conclusion that the conformation change does not take place within the area of the combining site but relatively far away, at the area of the hinge region and/or the Fc-fragment.
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  • 13
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 11 (1978), S. 464-465 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: A design study was made of a neutron small-angle scattering (SAS) instrument for use at Argonne National Laboratory's proposed Intense Pulsed Neutron Source, IPNS-II (Carpenter & Werner, 1976; Werner, 1977; Carpenter, 1977). The instrument design incorporates several features: a converging-slit collimator, wavelength band-limiting choppers, capacity for large samples, and a two-dimensional detector. Machine design-dependent parameters are considered in a Monte-Carlo code that produces estimates of the instrumental resolution function and available flux at the sample. It was found that the calculated flux on sample exceeds that at steady-state reactor instruments of comparable resolution.
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  • 14
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 11 (1978), S. 473-477 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: A comparative analysis of the sperm-whale myoglobin structure in the crystal and in solution has been carried out with the technique previously formulated by the authors which uses the large-angle X-ray diffuse scattering for investigating the protein structure in solution. A `modified cube method', correctly taking into account the cavities within the protein molecule accessible to the solvent, is proposed for an accurate estimate of the solvent influence and for calculation of the scattering intensities. A comparison of the theoretical myoglobin scattering curves with the experimental scattering curve of this protein obtained by Stuhrmann shows rather noticeable quantitative divergences, which can be eliminated by a small increase in the distance between the `hairpin' GH and the other part of the protein molecule. It is also shown that several other physically reasonable shifts of helices (or groups of helices) do not lead to an agreement between the experimental and theoretical scattering indicatrices.
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  • 15
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 11 (1978), S. 466-472 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: The density-contrast method, commonly used in X-ray (and neutron) small-angle scattering studies of macromolecules in solution, can yield a wealth of information if; (a) the solute is monodisperse and the solution is ideal: (b) each macromolecule in solution has a volume associated with it inside of which the density distribution is independent of the density of the solvent. More specifically it has been pointed out that in this case an expression of the molecular weight can be obtained which does not involve the partial specific volume, provided that the X-ray experiments are performed on an absolute scale. On the other hand, it is well known that X-ray scattering experiments on an ideal solution of identical macromolecules can yield the molecular weight for any composition of the solvent, provided solute, solvent and partial specific volumes are defined and measured at constant chemical potential. Therefore a combination of X-ray scattering and densimetry experiments allows one to verify to what extent condition (b) holds true. Such a set of experiments has been performed on Rhesus monkey low-density serum lipoproteins, the solvent being water containing variable amounts of NaBr. It is concluded that in this case condition (b) is fulfilled. Moreover several important aspects of the analysis of the X-ray scattering curves can be verified.
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  • 16
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 11 (1978), S. 479-482 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: The theory of the technique currently in use for measuring distances between subunits in macromolecular aggregates by neutron small-angle scattering is outlined. It is shown that estimates for the radii of gyration of subunits within aggregates can be extracted from neutron distance data, in addition to the distances themselves. The current status of efforts to apply these methods to determine the structure of the E. coli ribosome is discussed.
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  • 17
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 11 (1978), S. 483-484 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: Neutron-scattering studies of chromatin core particles in solutions containing various mixtures of D2O/H2O and small molecules (glycerol) show that the water closely associated (or bound) with the particles is largely in the outer DNA-rich regions. This confirms the fact that the particles contain a core composed of the hydrophobic regions of histone proteins.
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  • 18
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 11 (1978), S. 514-519 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: The use of the polymers tagged with heavy atoms in random positions along the chains (randomly tagged polymers) in small-angle X-ray scattering is proposed as a new method for measuring the chain conformations in concentrated solutions and in bulk polymers. The experimentally determined excess scattering from the tagged chains dispersed in the system is shown to be proportional to the scattering function of the hypothetical chains that have no tags but have the conformation of the tagged chains when the heavy atoms have sufficiently large scattering power. It has been experimentally verified that the effect of the tags on the chain conformation can be eliminated by the extrapolation of the apparent values, measured for a series of tagged polymers with various tag content, to zero tag content. The radii of gyration of the polystyrene chains (M = 1.1 × 105) in the bulk and in concentrated solutions in a good solvent and a θ-solvent have been determined. The chain dimension in a good solvent (toluene at 25°C) decreases rapidly first and then gradually approaches the unperturbed dimension with increasing polymer concentration. The dimension in a θ-solvent (trans-decalin at 21.2°C) is independent of the polymer concentration. The conformation of the polystyrene chains in the bulk was found to be a Gaussian coil.
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  • 19
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    Applied crystallography online 11 (1978), S. 525-530 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: Small-angle X-ray scattering from oriented mats and random suspensions of polyethylene single crystals has been studied. A modification of the Guinier equation for platelets was derived to accommodate the two-phase nature of polymer lamellae. This modification also permitted the modelling of various degrees of interaction between lamellae and suspending media. Dried crystal mats show an increase in fold period on contact with potential solvents. Crystals which have never been dried show no evidence of penetration of the fold surface by the same liquids. Apparently the drying process causes a reorganization of the surface of the lamellae. Since the fold surfaces of crystals in suspension are unaffected by the liquids used, it is reasonable to assume a `tight' fold surface model. Crystallinities calculated with this model are in excellent agreement with recent differential scanning calorimetric data on crystals kept in suspension.
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    Applied crystallography online 11 (1978), S. 519-523 
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    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: The study of semi-dilute polyelectrolyte solutions by small-angle neutron scattering shows that the correlation function S(q) of all the chains presents a peak for a value q = qh of the scattering vector q. This is taken as evidence for some organization among the elongated polyions. This phenomenon has been observed for a fraction of polymethacrylic acid of very low molecular weight. The experiments show essentially: (1) the progressive vanishing of the peak with the addition of a neutral salt at constant polyelectrolyte concentration; (2) the variation of qh with the polyelectrolyte concentration c, qh ∝ c1/2; (3) the decrease of the peak intensity as the charge density of the chain increases. These results, which indicate the important role of the electrostatic interactions on this organization phenomenon, are discussed in terms of a lattice model and a recently proposed isotropic model.
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  • 21
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 11 (1978), S. 535-539 
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    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: The concept of interface distribution functions [Ruland (1977). Colloid Polym. Sci. 255, 417–427] has been applied to the evaluation of the small-angle scattering of a series of polyethylene samples. The results indicate that the statistics of the lamellar stacking is not necessarily determined by next-neighbor interactions and that non-negligible volume fractions of amorphous domains outside the lamellar systems are observed in a number of samples.
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  • 22
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    Applied crystallography online 11 (1978), S. 551-557 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: Crystallization of a linear polyethylene from the melt was followed in situ with the ORNL 10-meter SAXS camera [Hendricks (1978). J. Appl. Cryst. 11, 15–30]. Specimens were rapidly cooled in the X-ray beam in tandem birdcage furnaces from 1̃80°C to temperatures between 115 and 126°C, and scattering patterns were recorded for 30 s in 50 s intervals. Because of this relatively high-speed data acquisition rate, it was possible to obtain data in time periods which were short compared to the rate of change of the scattering patterns. The SAXS curves showed shapes which changed continuously during crystallization. The scattering curves are the superposition of a zero-angle peak and a Bragg maximum. Guinier plots of the zero-angle peak manifest scattering by lamellae of constant thickness. The thickness value is nearly that expected for crystallites at these crystallization temperatures. A model in which skeletal spherulites form and then later fill in is consistent with these results. Decreasing SAXS intensity and changing Bragg peak intensities indicate crystal thickening during cooling to room temperature.
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  • 23
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    Applied crystallography online 11 (1978), S. 558-563 
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    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: The microdomain structure of polystyrene-polyisoprene A-B type block copolymers was analysed by small-angle X-ray scattering (SAXS) as an ideal model system for a pseudo two-phase solid structure. The structure was analysed in terms of spatial distribution, size, and the interracial structure of the dispersed domains of one component (A segments) in the matrix of the other (B segments). The SAXS analyses were performed with two collimating systems, a Rigaku Denki camera (essentially a four-slit system with the addition of Soller slits) and a Kratky camera, which had widely different slit-length and slit-width weighting functions and was used to investigate instrumental effects, especially the role of the Soller slits in the obtaining of reliable desmeared intensity data in the tail of the SAXS curve. Comparison of the results indicated that the Soller slits facilitate the accurate evaluation of the interfacial thickness from the desmeared intensity data in the tail. The accuracy of the infinite slit-height approximation and the effect of truncating the higher-order terms in Ih (the intensity associated with the interphase) on the estimated interfacial thickness are discussed. The infinite slit-height approximation leads to values 25–35% smaller than the exact value (23 Å), and the truncation also leads to a value of the interfacial thickness smaller (19 Å) than the value (23 Å) based on the full analysis. The value obtained is in good agreement with the values predicted from the statistical-mechanical theories of block copolymers in bulk.
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  • 24
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    Applied crystallography online 11 (1978), S. 572-577 
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    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: Isothermal decomposition of a Au-60 at.% Pt alloy, quenched from the solid as well as the liquid state, has been studied with the D11 neutron small-angle scattering spectrometer at ILL, Grenoble. An incident neutron wavelength of 6.7 Å was used and measurements were carried out in the range of scattering vector [β = 4πsin θ/λ] from 2.8 × 10−2 to 21 × 10−2 Å−1. The preliminary results indicate that decomposition of this alloy at 550°C takes place by a spinodal mode, although deviations were observed from linear spinodal theory, even at very early times. Slower aging kinetics were observed in liquid-quenched alloy as compared with solid-quenched. Liquid quenching is more efficient in suppressing quench clustering than is solid quenching. However, liquid quenching yields an extremely fine-grained material, which thereby enhances discontinuous precipitation at grain boundaries, competing with decomposition in the bulk. A Rundman–Hilliard analysis was used for the early stages of the spinodal reaction to obtain an interdiffusion coefficient of the order of 10−16 cm2 s−1 at 550°C for the solid-quenched alloy.
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    Applied crystallography online 11 (1978), S. 564-568 
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    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: Two methods for performing small-angle electron scattering (SAES) experiments in transmission electron microscopes are described: the long-camera-length method and the selected-area-diffraction method. It is shown experimentally that angular resolutions of a few microradians and a few tenths of milliradians, respectively, are easily obtained by these two methods. A number of examples of the application of SAES to problems in materials science are presented. The use of new high-brightness electron sources is expected to produce significant increases in angular resolution, and the use of electron-energy analyzers will permit the separation of most of the inelastic contribution to the SAES intensity distribution.
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    Applied crystallography online 11 (1978), S. 583-588 
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    Topics: Geosciences , Physics
    Notes: The creep properties in high-temperature alloys are dependent on the presence of second and higher phase components. In particular in the nimonic group of alloys the size distribution and concentration of the γ′ phase are crucial factors in the resistance to creep. A possible mechanism for degradation of creep resistance is the Ostwald ripening of the γ′ phase. A sample of Nimonic 105 (Trademark of Henry Wiggin and Co. Ltd) was subjected simultaneously to a stress of 500 MPa and a temperature of 800°C in situ in the beam using a specially developed cell on the small-angle scattering facility (D 11A) at the Institut Laue Langevin. Scattering patterns were taken continuously and spectra were recorded every ̃20 min; the macroscopic creep was also recorded. Measurements were taken up to the point of fracture. A peak in the intensity was observed at a scattering vector κ (= 4π sin θ/λ) of 0.005 Å−1 which is believed to be the lowest value at which such an effect has been observed in alloys. The observed variation in the scattering after treatment for multiple scattering and absorption corrections is discussed in terms of particle size and size distribution.
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    Applied crystallography online 11 (1978), S. 658-661 
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    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: A double-mirror monochromator in which one of the mirrors is considerably longer than conventionally employed has been used to collect diffraction data from crystalline tobacco mosaic virus (TMV) protein (unit cell: 224 × 228 × 174 Å). Considerable improvements in speed of data collection are observed over both customary focusing optics and pinhole collimation. Quantitative comparisons are made of the quality of data collected from TMV protein by this method and by the use of nickel-filtered radiation.
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    Applied crystallography online 11 (1978), S. 654-657 
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    Notes: Correlation between the symmetry of the two-dimensional flux-line lattice (FLL) and the real crystal lattice (CL) has been studied in a superconducting niobium sphere by means of small-angle neutron diffraction. A double-perfect-silicon-crystal diffractometer enabled precise determination of the three interfluxoid distances corresponding to the FLL basic cell. A systematic study of the anisotropic behavior was made as a function of temperature and magnetic field amplitude for fields parallel to a few high-symmetry CL axes in the (1{\bar 1}0) plane. In addition, at T = 4.30 K progressive deformation of the FLL was studied as the sample was rotated in the (1{\bar 1}0) and (100) planes. The FLL was found to be hexagonal only for fields parallel to the threefold CL axis. Twofold symmetry prevailed for other CL directions in these planes except near the fourfold axis, where either of two distorted triangular lattices existed, preserving the reflection symmetry in composite, but not individually. When compared to current models for fluxoid-CL interactions, the present results show that no theory predicts the observed behavior quantitatively under general conditions, but some models agree well for certain high-symmetry CL axes.
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  • 29
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    Applied crystallography online 11 (1978), S. 669-669 
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    Notes: Some multiplicities for the Laue class \bar 31m are not correct in several standard texts.
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  • 30
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    Applied crystallography online 11 (1978), S. 650-653 
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    Notes: The double-perfect-crystal small-angle diffraction technique enables measurement of scattering angles to within an accuracy of 0.3′′ of arc. At a wavelength of 2.55 Å, this provides a resolution of 3 × 10−6 Å−1 in the scattering vector. This technique has been used to study the anisotropic behavior of the critical parameters B0 and Hc1, characteristic of the first-order magnetic phase transition which occurs in low-κ type II superconductors. Magnetic fields were applied parallel to several crystal axes in the (1{\bar 1}0) and (100) planes of a large single-crystal sphere of pure niobium, resulting in well defined flux-line lattices (FLL). Measurement of the FLL cell area in the intermediate, mixed-state-field region gives the equilibrium flux density B0, which results from an attractive interaction between fluxoids. In addition, field variation of the scattered neutron intensity allows measurement of the transition field between the mixed state and intermediate mixed state. This transition field is related to the lower critical field Hc1 and enables its determination to a precision of 0.2%. Data at T = 4.3 K display a small anisotropic effect of about 2% in B0 and 1% in Hc1. Although orientation effects of this magnitude are difficult to resolve by bulk measurements, the neutron data are in accord with magnetization data. The temperature dependence of these parameters is found to be in qualitative but not quantitative agreement with current theoretical models.
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  • 31
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    Applied crystallography online 11 (1978), S. 669-669 
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    Notes: An amendment to a computer program for determining multiplicities of powder reflections [Rouse & Cooper (1977). J. Appl. Cryst. 10, 134–135] has been made to correct an error in the multiplicity values given for some reflections for space groups with {\bar 3}1m Laue symmetry, which exists in some of the standard texts.
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  • 32
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    Applied crystallography online 11 (1978), S. 662-668 
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    Notes: A method is described for precision measurement of lattice parameters in cubic crystals, interplanar spacings and angles between crystallographic directions for single crystals of any system. The minimum measurable values of angle between crystallographic directions, Δd/d and Δa/a have been found to be ̃105 rad, ̃3 × 10−5, and ̃5 × 10−5, respectively.
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    Applied crystallography online 11 (1978), S. 670-671 
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    Notes: The cell constants of recrystallized diphenylsilanediol were refined from precision powder data taken with Cr Kα1 (2.28962 Å): a = 14.493 (5); b = 15.012 (6); c = 9.897 (6) Å; α = 100.84 (9); β = 100.01 (5); γ = 120.77 (5); U = 1721.6 Å3; Z = 6; Dm (25°C) = 1.255 (3); Dx = 1.252 g cm−3.
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    Applied crystallography online 11 (1978), S. 671-671 
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    Applied crystallography online 11 (1978), S. 673-674 
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    Applied crystallography online 11 (1978), S. 675-680 
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    Notes: The simulation of the photography remains the worst part in the calculation of transmission electron micrographs and X-ray topographs. Storage displays have been used to enhance this part of the process and the different possibilities of these screens studied. The quality of all simulations has been substantially increased by using these displays, which are now in common use.
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    Applied crystallography online 11 (1978), S. 684-687 
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    Notes: A high-resolution energy-dispersive diffractometer is described, which uses a synchrotron source and a scanning channel-cut silicon crystal. The technique is demonstrated with a powdered sample of BaTiO3 and analysis of the profiles demonstrates the anomalous particle-size effect reported by Anliker, Brugger & Känzig [Helv. Phys. Acta (1954), 27, 99–124].
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  • 38
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    Applied crystallography online 11 (1978), S. 719-720 
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    Applied crystallography online 11 (1978), S. 720-720 
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    Applied crystallography online 28 (1995), S. 20-25 
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    Notes: This work is devoted to a new generation of cold-neutron interferometers based on bidimensional diffraction. The use of multilayer coatings in the classical Ioffe difffraction-grating neutron interferometer is proposed. This interferometer combines the properties of two periodic structures, namely the dispersion by a diffraction grating and the high reflectivity ensured by the multilayer coating. All the cold-neutron interferometer devices (two diffraction gratings and two mirrors) must be multilayered with Ni–Ti or Fe–Ge for unpolarized or polarized neutron interferometry experiments, respectively. The computed results, giving the characteristics of the multilayer-coated amplitude diffraction grating are discussed within a kinematic model. An Ni–Ti multilayered amplitude diffraction grating for use at λ = 5 Å is presented as an example.
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    Applied crystallography online 28 (1995), S. 49-52 
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    Notes: The form of the transmission factor for sample geometries encountered in X-ray and neutron fibre diffraction studies is considered. Transmission factors obtained by Monte Carlo experiments and a simple first-order approximation are compared and agree to within 1% for studies of the distribution of water and cations around DNA. The first-order approximation has the advantage of being simple and less computationally expensive.
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    Notes: The synchrotron X-ray results reported here are from the first high-resolution triple-crystal diffraction experiments performed at the Australian National Beamline Facility (ANBF). At the centre of the ANBF is a multipurpose high-resolution two-axis vacuum X-ray diffractometer. The Si(111) sample studied has been implanted with B+ ions through a one-dimensional SiO2 strip pattern with a 5.83 μm period and 4 μm open region, to produce a sample with a periodic superstructure in the lateral direction. The triple-crystal data were collected in the form of two-dimensional intensity maps in the vicinity of the 111 Bragg peak. Results collected in both air and vacuum are compared, as are results with and without the oxide layer. The data collected in vacuum indicate that it is possible at the ANBF to measure lattice distortions perpendicular to the sample surface with a 50 Å depth resolution.
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  • 43
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    Applied crystallography online 28 (1995), S. 66-67 
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    Applied crystallography online 28 (1995), S. 68-68 
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    Applied crystallography online 28 (1995), S. 96-104 
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    Notes: Orthorhombic (O1, O2 and O3) and monoclinic (M1 and M2) phases are the crystalline approximants of the Al–Cu–Fe–Cr decagonal quasicrystal. The structures of these crystalline phases can be described using three subunits, which are derived from the O3 structure. As an example, the structural model of the O1 phase is presented in detail. This model agrees with the X-ray powder diffraction pattern and the high-resolution electron image of the O1 phase.
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  • 46
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    Applied crystallography online 28 (1995), S. 115-120 
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    Notes: On the basis of known equations for calculating X-ray diffraction intensities from a given number of unit cells of a crystal phase in polycrystalline material, as due to: (i) Bragg reflections; (ii) average diffuse scattering caused by thermal plus first-kind disorder; and (iii) incoherent scattering, a relationship has been found that ties, in the Rietveld analysis, the Bragg scale factor to a scale factor for `disorder' as well as incoherent scattering. Instead of fitting the background with a polynomial function, it becomes possible to describe the background by physically based equations. Air scattering is included in the background simulation. By this means, the refinement can be carried out with fewer parameters (six fewer than when a fifth-order polynomial is used). The DBWS-9006PC computer program written by Sakthivel & Young [(1990), Georgia Institute of Technology, Atlanta, GA, USA] has been modified to follow this approach and it has been used to refine the crystal structures of the cubic form of Y2O3 and of α-Al2O3. Peak asymmetry has been described by a function based on an exponential approximation. The results from refinements using polynomial physically based background function are, in terms of final structural parameters and reliability indices, very close to each other and in agreement with results reported in the literature. The reconstruction and optimization of the background scattering by means of physically based equations helps the implementation in the Rietveld code of other possible specific diffuse scattering contributions, such as that due to an amorphous phase.
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  • 47
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    Applied crystallography online 28 (1995), S. 146-159 
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    Notes: A method of X-ray line-broadening analysis is presented whereby the coherence length and microstrain contributions can be calculated using a Monte Carlo interference-function-fitting algorithm. The method is based on the `column-like' crystal model and can be applied to both single and multiple-order reflections. Examples on simulated diffraction peaks, deformed face-centred-cubic palladium powder and heavily textured deformed body-centred-cubic low-carbon-steel sheets are presented and comparisons are made with currently applied methods.
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  • 48
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    Applied crystallography online 28 (1995), S. 279-288 
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    Notes: Numerical image treatment has been used for the enhancement and the analysis of synchrotron white-beam topographs. Images are recorded either during the experiment by means of an X-ray-sensitive camera or after the experiment from photographic films. Filters are designed to avoid artefacts such as the Gibbs effect. Filtering has been applied to the study of the propagation of surface acoustic waves in piezoelectric materials and ferromagnetic domains in Fe–Si crystals, illustrating the interest of Fourier filtering for a deep analysis of X-ray topographs.
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    Applied crystallography online 28 (1995), S. 69-77 
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    Notes: The average number of reflections for radiation transmitted by a straight cylindrical channel can be determined analytically for an input beam for which the divergence has polar symmetry. For the case of an incident beam with a divergence of Cartesian symmetry (for example, the output from a rectangular neutron guide), the number of reflections can be calculated only if the maximum divergence is less than the critical angle of the cylindrical channel. For larger divergences, the requirement that the glacing angle is less than the critical angle does not allow a simple analytic solution. This paper reports the calculation of the number of reflections using an approximation and makes comparisons with a numerical simulation that gives an estimate of the exact result.
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    Applied crystallography online 28 (1995), S. 105-114 
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    Notes: A numerical calculation method for determining the resolution functions for radially symmetric collimation and scattering is described. In the present approach, the total number of integrations is reduced to four by use of the radial symmetry of the geometry. Furthermore, the beam-stop shadowing effect is included exactly. A typical calculation can be completed in minutes on current personal computers. An interactive computer program allows the user to enter the experimental parameters such as aperture size and wavelength spread, allowing smearing calculations to be handled routinely as a `black box' operation. The exact smearing treatment is compared both to an improved technique involving Gaussian resolution functions where corrections for the beam stop are included and to results from Monte Carlo simulations. In most experiments, the use of a Gaussian distribution to approximate the resolution is preferred on account of its ease of calculation. But in a few cases, such as Porod scattering, the present more extensive numerical calculation or inclusion of the developed beam-stop-shadowing correction factors into a Gaussian scheme are needed for an adequate prediction of the smearing effects.
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    Applied crystallography online 28 (1995), S. 141-145 
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    Notes: This paper reports synchrotron X-ray powder diffraction and high-resolution electron microscopy studies of the structural arrangement in γ-Fe2O3. Powder diffraction data as well as high-resolution electron microscopy show that the basic structure of γ-ferric oxide possesses cubic symmetry (space group P4332), whereas the ordered distribution of the cation vacancies on the octahedral positions results in the formation of the tetragonal superlattice (space group P41212). The character of the superstructure orientation with respect to the developed planes of the γ-Fe2O3 microcrystals obtained by different preparative techniques is also discussed.
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    Applied crystallography online 28 (1995), S. 168-188 
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    Notes: The basic defect structure of solution-grown single crystals of ammonium sulfate and changes to it as it undergoes a paraelectric to ferroelectric phase transition at 223 K are investigated using conventional Lang and white-synchrotron-radiation X-ray topography. Topographs of thick (ca 1 mm) plates reveal the existence of lattice strain prior to transformation. The shape of the phase boundary is revealed from studies of thinner plates (ca 0.3 mm). These show sharply defined zigzag-shaped boundaries between the paraelectric and the ferroelectric phases in plates cut parallel to (010) and (001). Cracks and dislocation loops (Burgers vector [001]) generated by plastic deformation are found to originate from the apices of the zigzag boundaries. No distinct phase boundaries were observed in (100) plates. The preferred (energetically favoured) orientations (i.e. the zigzag segments) of the phase boundaries in (010) and (001) as well as their blurred appearance in (100) plates are explained by the specific properties of the strain tensor associated with the transition. Ferroelectric domains have also been detected by the faint dynamical X-ray contrast of their boundaries (180° walls).
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    Applied crystallography online 28 (1995), S. 242-243 
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    Applied crystallography online 28 (1995), S. 244-244 
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    Applied crystallography online 28 (1995), S. 245-246 
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    Applied crystallography online 28 (1995), S. 246-246 
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    Applied crystallography online 28 (1995), S. 274-278 
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    Notes: Calculations of powder diffraction peaks using a model of tiny (diameter a few nm) spherical crystals log normally distributed in size with and without surface relaxation are presented. The calculated peak shapes are more nearly Gaussian than Cauchy (Lorentzian). Surface relaxation can produce small variations in peak positions, order-dependent peak widths and asymmetric tails. The latter may be quite pronounced in the smaller particles and are qualitatively similar to recent data taken on nanometre-sized crystals. This suggests that comparison of model calculations with X-ray powder data of single peaks or, preferably, entire diffraction patterns (perhaps as part of a Rietveld refinement) may allow probing of surface atom positions in nanometre-sized particles.
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    Applied crystallography online 28 (1995), S. 302-305 
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    Notes: The conditions for appearance of the isoscattering points of one- and two-dimensional systems have been theoretically derived using the ideal models of oriented membranes and fibers. The position s* of the isoscattering point of a one-dimensional system is given by s* = n/(2R0), where n is a positive integer and 2R0 is the thickness of the membrane. For a two-dimensional system, the position s* is given by J1(2πs*R0) = 0, where J1 is the first-order Bessel function and R0 is the radius of the fiber.
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    Applied crystallography online 28 (1995), S. 659-659 
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    Applied crystallography online 28 (1995), S. 655-658 
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    Notes: This communication gives the asymmetric factor b and deviation parameter η describing the diffraction geometry in a more general way including very asymmetric scattering arrangements. Darwin's parameter Y defined on the dispersion surface and the associated deviation parameter ηY given by the Takagi–Taupin equations are proposed to characterize the angular deviation from the exact resonance of Bragg diffraction. With respect to ηY of a high accuracy, the validity of conventional forms of the deviation parameter is further discussed.
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    Applied crystallography online 28 (1995), S. 666-672 
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    Notes: X-ray rocking-curve analysis of implanted silicon is commonly used to investigate damage accumulation with increasing ion dose. The damage build-up is observed by the trends of either the maximum of the lattice strain normal to the surface (ε.⊥) or the depth integral of the ε.⊥ profile. However, for doses high enough to produce a buried amorphous layer, the determination of the peak value of the ε.⊥ depth profile, and hence of its integral, is not possible. This is demonstrated by means of a simple diffraction model which describes the amorphous layer as a material for which the structure factor is reduced to zero by sufficiently high values of the static Debye-Waller factor and for which the expansion u normal to the surface is given by the product of the fractional change of the interplanar spacing of the perfect crystal (ε.⊥α) and the thickness of the amorphous layer (tα). Since this expansion can be written as u = ε.⊥αtα = (n + x)d, where n is an integer (n = 0, 1, 2, ...), 0 ≤ x 〈 1 and d is the spacing of the diffraction planes of the perfect crystal, the diffraction model shows that, for given thickness tα and fraction x of d, there exists a discrete, in principle infinite, set of u values able to give identical rocking curves. This prevents the rigid outward displacement of the damaged surface crystalline region with respect to the substrate from being determined.
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    Applied crystallography online 28 (1995), S. 707-716 
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    Notes: Neutron diffraction data collected from ferrosilicon alloy powders have been analysed using the Rietveld profile-refinement method in order to perform a quantitative determination of the phase volume fraction. The results obtained have been compared with those determined from other methods such as imaging analysis, chemical analysis and phase-diagram calculation by a thermodynamic approach. For low phase volume fractions, the Rietveld profile refinement of the neutron-powder-diffractometer data gives results that are more accurate than those from imaging analysis and that are more representative at the ingot scale than those from chemical analysis, owing to the greater quantity of powder analysed. As concerns the thermodynamic calculations, two phase volume fraction determinations may be performed: quantitative, at equilibrium, and qualitative, out of equilibrium.
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    Applied crystallography online 28 (1995), S. 745-752 
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    Notes: A new imaging-plate diffractometer of the Weissenberg-camera type with an adjustable multilayer-line screen system (IPD-WAS) has been developed. Prior to data collection, the IPD-WAS automatically aligns the axis of a sample crystal and sets the multilayer-line (MLL) screens. The MLL-screen system is adaptable to a wide range of cell parameters of the sample crystals, and is advantageous for taking photographs in a wide rotation angle with a low background level. For Weissenberg photography, the IPD-WAS system uses two cylindrical imaging plates (IPs). The IPs are read two-dimensionally by rotary and transverse mechanisms. The rotary readout system has nonuniformity of response less than 1.4%, efficiency near 100% for Cu Kα radiation, a dynamic range of 1:106 and spatial resolutions of 220 and 200 μm in the two directions. Owing to the good performance of the adjustable MLL screen system and the rotary readout system, the IPD-WAS achieves a data acquisition time of about l h with reflection data of sufficient quality (Rmerge = 2.3% for a standard sample crystal), which is suitable for time-resolved X-ray crystallography. The IPD-WAS also enables faster crystal structure determinations of small molecules, including unstable crystals.
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 28 (1995), S. 829-834 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: In order to directly observe the structure of enzyme intermediate complexes that form during turnover, one must ensure the homogeneous and complete accumulation of the intermediate during the collection of diffraction data. In the case of steady-state Laue experiments, the accumulation of the intermediate is dictated by the rate of substrate diffusion throughout the crystal, compared with the rate of turnover and disappearance of a rate-limited catalytic intermediate. This paper describes a simple quantitative method for measuring substrate diffusion and binding within an enzyme crystal. The set-up consists of a light source, specific bandpass filters, a crystallographic flow cell, a syringe pump, a charge-coupled-device color video camera and a workstation with a frame-grabber card for collection and digitization of images and subsequent processing of data. By this technique, any diffusion and binding process in a protein crystal leading to a visible absorbance shift may be accurately monitored and quantified during data collection. This method offers the crystallographer an inexpensive and simple alternative to the use of a single-crystal microspectrophotometer to measure the relatively slow process of diffusion.
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 28 (1995), S. 847-852 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: WPDB version 2.0 is a Microsoft-Windows-based program for browsing and interrogating native and derived structural features of biological macromolecules using data obtained from the Protein Data Bank (PDB). Major features of WPDB are a 20-fold compression of PDB files and query and analysis tools. The latter permit the geometric and sequence properties of structures to be analyzed individually or through comparative analysis. The object-oriented software design provides a high level of interaction between display windows, which facilitates information discovery. Three examples are given to illustrate the capabilities of the software, namely: location of the distribution of the most hydrophobic residues in the acid proteases; exploration of the geometric features of a 4-helix bundle motif; and examination of the effect of antibody binding by comparison of a neuraminidase with a neuraminidase-antibody complex. Additional details are available to World Wide Web (WWW) users at the URL http://www.sdsc.edu/CCMS/ Packages/wpdb.html.
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 28 (1995), S. 856-857 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: A new crystal mounting device for cryogenic macromolecular crystallographic experiments is described. The device is made from a conventional capillary tube by cutting it into a thin ring. This device realizes the transmission of X-rays in any direction and a crystal can be aligned using the wall of the ring.
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 28 (1995), S. 782-785 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: The iso-zero-angle-intensity point (abbreviated as isoZAI point) is a specific point at which X-ray zero-angle intensities of samples with different structures take a constant value. The isoZAI point was first observed in X-ray contrast-variation studies of a homologous series of micelles. The condition for appearance of the isoZAI point has been theoretically derived by consideration of samples with inhomogeneous internal structure. The condition is given by where νij and ρij are the volume and electron density of jth internal domain of the ith sample (1 ≤ i ≤ N, 1 ≤ j ≤ M), respectively. ρ0* denotes the position of the isoZAI point on the electron-density scale. The isoZAI point was found to give useful information for analysis of X-ray or neutron small-angle scattering data measured by the contrast-variation method.
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 28 (1995), S. 820-826 
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    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: The parasitic scattering of several materials used as windows in small-angle scattering experiments, including IF-1 beryllium, Kapton, Mylar, mica and glass has been measured over the q range 0.05–2.0 nm−1 with Cu Kα radiation (q = 4πsinθ/λ, 2θ = scattering angle). Based on the criteria of high strength, high transmission and low parasitic scattering, the best material was found to be IF-1 beryllium.
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 28 (1995), S. 839-842 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: Complete numerical simulations of X-ray back-reflection Laue-grams have been carded out. The main factors that affect the intensities of Laue-gram spots have been evaluated. The proposed procedure is general and can be applied to any crystalline material and for any kind of detector and radiation source. The computational requirements are minimal and inexpensive. Excellent agreement between the experimental and the simulated Laue-grams are observed. To demonstrate the potential of these procedures, the case of LiNbO3 is presented here. Exact replication of the Laue-gram for LiNbO3 has been obtained.
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 28 (1995), S. 858-860 
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 28 (1995), S. 860-860 
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    Acta crystallographica 51 (1995), S. 23-26 
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