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  • Wiley  (17,554)
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  • American Physical Society  (9,158)
  • International Union of Crystallography (IUCr)  (2,747)
  • 1995-1999
  • 1980-1984
  • 1975-1979  (43,667)
  • 1925-1929
  • 1978  (22,426)
  • 1976  (21,241)
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  • 1975-1979  (43,667)
  • 1925-1929
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  • 1
    Electronic Resource
    Electronic Resource
    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 9 (1976), S. 14-17 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: A detailed description of an automatic low-temperature apparatus to be used in single-crystal diffractometry is given. The crystal is cooled by a stream of nitrogen gas. Prevention of ice formation on the crystal is achieved by heating the outer parts of the gas stream by a conical metal device. The unit-cell dimensions of α-quartz have been determined in the temperature range 86–298 K with this apparatus on a four-circle diffractometer of type CAD-4.
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  • 2
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 9 (1976), S. 34-38 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: X-ray reflection topographs were taken of a zinc surface oriented about 1° from a basal plane. Basal dislocations are revealed in the topographs, and their apparent depth was determined using stereo pairs of topographs. The apparent depths observed in a complimentary pair of topographs using 10\bar 13 and \bar 1013 reflections were significantly greater than those observed in an asymmetric pair of topographs in which the same 10\bar 13 reflection was used. This difference is attributed to shifts of the image with respect to the dislocation position. Quantitative estimates of the image shifts and the actual depths of the observed dislocations are obtained from the measurement of apparent depths. Dislocations are visible over the range of depths from 1.7 to 4.5 μm.
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  • 3
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 9 (1976), S. 253-254 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: A set of Fortran programs for radial distribution function analyses of X-ray and electron diffraction data of liquid and amorphous samples is available. The programs relate, first, to the formation of a reduced intensity function, F(K) ≡ (I − 〈f2〉)/〈f〉2, where I is the coherent scattered intensity in electron units, K is 4π sin &thgr;/λ, and 〈f〉 is the average of the scattering factors. The experimental radial distribution function G(r) = 4πr[ρ(r)−ρ0], is derived as the Fourier sine integral of F(K).
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  • 4
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 9 (1976), S. 257-258 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
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  • 5
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 9 (1976), S. 286-290 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: A cryostat has been designed for an energy-dispersive X-ray diffractometer so that the specimen can be measured between 1.48 K and room temperature. Three powder samples can successively be measured at a fixed temperature by rotating the cryostat in steps of 120°. This design is very suitable particularly for detecting a slight change or difference, if any, in lattice constant among samples. A typical example is described of detecting the difference in lattice constant between 92Mo and 100Mo.
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  • 6
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    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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  • 7
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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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  • 8
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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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  • 9
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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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  • 10
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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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  • 11
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 9 (1976), S. 254-256 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: A Fortran program for plotting contour maps of texture functions is described. The program works at high speed and is very flexible in application. For input the values of the texture function, which have been measured or calculated on a grid of mesh points, are required. From these data, the single-level lines of a contour map are calculated and plotted. Format and caption of the contour map as well as the marking of the level lines can be individually chosen. In the present paper the program is applied to direct and inverse pole figures as well as to a three-dimensional orientation distribution function (ODF) of a silver sheet deformed by 99.3%.
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  • 12
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 9 (1976), S. 258-258 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
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  • 13
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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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  • 14
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 9 (1976), S. 507-508 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: The compounds diphenyl tin sulphide trimer and n-dibutyl(ethylene-1,2-dithiol)stannane crystallize into space groups P21 and C2 respectively. The unit-cell parameters are reported.
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  • 15
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 9 (1976), S. 361-364 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: Crystal data (from single-crystal measurements) are reported for 19 different crystalline π-molecular compounds, representing 16 different chemical species (three polymorphic pairs are included). 13 of these molecular compounds have equimolar compositions, five have donor:acceptor ratios of 1:2 and the remaining one has composition (fluorene)3 :( 1,3,5-trinitrobenzene)4.
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  • 16
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 9 (1976), S. 369-370 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
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  • 17
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 9 (1976), S. 415-416 
    ISSN: 1600-5767
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  • 18
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 9 (1976), S. 417-417 
    ISSN: 1600-5767
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  • 19
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 9 (1976), S. 417-418 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
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  • 20
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 9 (1976), S. 419-423 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: A semi-automated system has been developed for identifying the components of a crystalline mixture according to correlations between the diffraction pattern of the mixture and the Hanawalt index of the Powder Diffraction File. The system is designed for use in the laboratory with modest computing facilities, e.g. a disc or tape-based 16 K mini-computer. In the computerized stage of the system those components which cannot contribute to the measured pattern are automatically eliminated. Subsequent manual interpretation of the results of the computer search, preferably with the support of a semi-quantitative elemental analysis, further reduces the number of possibilities.
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  • 21
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 9 (1976), S. 433-440 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: The total X-ray intensity as a function of h (h is the radial coordinate in reciprocal space), scattered by an isotropic system of particles of equal shapes but of different sizes R, can, under certain conditions, be expressed as an integral over the particle size distribution function D(R), multiplied by a common single-particle function of hR which can be calculated from the assumed particle shape. In the first method D(R) is calculated from this relation by the method of least squares, in which values of D at a limited number of particle sizes are the unknowns. To avoid oscillations in the D curve, constraints are imposed on the D values. The proper weight to be assigned to these constraints must be determined by trial and error. The method has been adapted to suit various assumptions and requirements as to the shape of the particles, the type of distribution function to be calculated, and experimental conditions (slit or pinhole focusing). The second method is essentially the one described by Schmidt, Weil & Brill [X-ray & Electron Methods of Analysis, pp. 86–100. (1968), New York: Plenum], which, however, is adapted to the use of slit-smeared intensities. Both methods may give rise to artefacts in the calculated distribution functions in the range of the smallest particle sizes, which are sensitive to the setting of the various parameters and to experimental errors. However, the position and shape of the main maxima can usually be determined quite well. The agreement between the results obtained by the two methods is satisfactory.
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  • 22
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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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  • 23
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 9 (1976), S. 512-512 
    ISSN: 1600-5767
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  • 24
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 9 (1976), S. 512-512 
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  • 25
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 9 (1976), S. 513-513 
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  • 26
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 11 (1978), S. 293-294 
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  • 27
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    Applied crystallography online 11 (1978), S. 293-293 
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 11 (1978), S. 294-294 
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  • 29
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    Applied crystallography online 11 (1978), S. 346-375 
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    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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    Applied crystallography online 11 (1978), S. 477-477 
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    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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    Applied crystallography online 11 (1978), S. 464-465 
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    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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  • 32
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    Applied crystallography online 11 (1978), S. 473-477 
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    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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    Applied crystallography online 11 (1978), S. 466-472 
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    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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    Applied crystallography online 11 (1978), S. 479-482 
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    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
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    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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  • 35
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    Applied crystallography online 11 (1978), S. 483-484 
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    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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    Applied crystallography online 11 (1978), S. 514-519 
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    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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  • 37
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    Applied crystallography online 11 (1978), S. 525-530 
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    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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  • 38
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    Applied crystallography online 11 (1978), S. 519-523 
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    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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  • 39
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    Applied crystallography online 11 (1978), S. 535-539 
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    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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  • 40
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    Applied crystallography online 11 (1978), S. 551-557 
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    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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  • 41
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    Applied crystallography online 11 (1978), S. 558-563 
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    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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  • 42
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    Applied crystallography online 11 (1978), S. 572-577 
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    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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  • 43
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    Applied crystallography online 11 (1978), S. 564-568 
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    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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  • 44
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    Applied crystallography online 11 (1978), S. 583-588 
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    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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  • 45
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    Applied crystallography online 11 (1978), S. 658-661 
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    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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  • 46
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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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  • 47
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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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  • 48
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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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  • 49
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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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  • 50
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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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  • 51
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    Applied crystallography online 9 (1976), S. 370-370 
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    Applied crystallography online 9 (1976), S. 371-371 
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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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    Applied crystallography online 9 (1976), S. 416-416 
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    Applied crystallography online 9 (1976), S. 417-417 
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    Applied crystallography online 9 (1976), S. 418-418 
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    Applied crystallography online 9 (1976), S. 418-418 
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    Applied crystallography online 9 (1976), S. 424-428 
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    Notes: In the computer indexing of powder diffraction patterns, an advance estimate of the volume of the unit cell is extremely valuable. This paper describes a method for estimating it directly from powder-pattern data for the case of triclinic materials. The method involves an easily prepared graphical plot, the slope of which is proportional to the unit-cell volume. First, the diffraction lines are numbered consecutively, starting with the largest d value (N = 1). A plot is then made of 1/N versus d3. Theoretically, the resulting line has a slope of 3/(2πV) = 0.4775/V for triclinic compounds, where V is the unit-cell volume. Examination of the graphs plotted for a number of triclinic materials where the experimental data are of high quality shows that the slope consistently falls around 0.60/V. Hence, the volume of the unit cell and/or the calculated density can be estimated. In addition, this analysis gives a numerical measure of the fraction of possible diffraction lines actually observed.
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    Applied crystallography online 9 (1976), S. 444-453 
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    Notes: A description is given of the computer-controlled triple-axis neutron spectrometer system installed at the PLUTO reactor at Harwell. Following the operation of the original system for several years a number of major improvements have been made which have resulted in a highly reliable system which provides the users with very powerful and extensive facilities. Following a general description of the modified spectrometer, details are given of the new computerized control system which utilizes a CAMAC modular interface and the functions of the various programs which are now available to the users are described.
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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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    Acta crystallographica 34 (1978), S. 1-2 
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    Topics: Chemistry and Pharmacology , Geosciences , Physics
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    Acta crystallographica 34 (1978), S. 27-30 
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    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: A probabilistic theory is described which is able to estimate in P{\bar 1} the values of two and three-phase structure seminvariants respectively.
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    Acta crystallographica 34 (1978), S. 31-38 
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    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The use of magic integers in phase determination is examined in the light of the theory of Main [Acta Cryst. (I 977). A33, 750-757]. The integers may be used in the economical search of an n-dimensional function of the phases. An interpolation procedure in the n-dimensional phase space allows the use of integer sequences of quite high error, with a consequent reduction in the magnitudes of the integers used. The number of variables to be associated with the magic-integer sequences is also examined. It is found that this number has virtually no effect on either accuracy of phase representation or on computing time. The range of one of the variables can be restricted, where necessary, in order to define the enantiomorph, thus using several phases simultaneously to give a strong enantiomorph definition. A convergence procedure is described for choosing the phases to be represented by magic integers. Magic integers may also be used to choose sets of phase values for the reflexions used in MULTAN to start phase determination. This replaces the more usual quadrant permutation method and results in large savings in the number of starting sets to be explored. MULTA N is thus made more powerful for the same computing time as before.
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    Acta crystallographica 34 (1978), S. 43-47 
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    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The real part, f' of the anomalous dispersion correction to atomic structure factors was measured by using Pendellösung fringes for Si 220 and {\bar 22}0 reflections in the wavelength range from Cu Kα1 to Rh Kα1. In order to avoid ambiguity in the Thomson-scattering term due to the nature of the bonding, the quantity (f'X - f'Ag) was compared with the available theoretical calculations. In this expression, f'X and f'Ag are the corrections for radiation X and Ag Kα1, which is used as the standard, respectively. The present experimental results fit best the values calculated by Cromer & Liberman [J. Chem. Phys. (1970), 53, 1891-1898].
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    Acta crystallographica 34 (1978), S. 48-51 
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    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: By the use of convergent-beam and critical-voltage measurements it has become possible to measure the crystal potential to an accuracy of about 10-3. The possibility that the contribution from virtual inelastic scattering is greater than the errors in these experiments is examined and it is shown that only virtual scattering from single-electron excitations need be considered. Estimates are given for the Fourier coefficients of the virtual inelastic scattering potential for silicon, copper and germanium and these are compared with the errors in the critical-voltage experiments of Hewat & Humphreys [High Voltage Electron Microscopy (1974), edited by P. R. Swann, C. J. Humphreys & M. J. Goringe, pp. 52-56. London and New York: Academic Press]. It is concluded that the virtual inelastic scattering contribution is less than the experimental errors.
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    Acta crystallographica 34 (1978), S. 52-54 
    ISSN: 1600-5724
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Expressions are developed for the components of the linear Lagrangian, linear Eulerian, finite Lagrangian (Green's), and finite Eulerian (Almansi's) strain tensors in terms of a crystal's lattice parameters before and after a deformation. The development has been undertaken with the concepts and notations of linear algebra.
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    Acta crystallographica 34 (1978), S. 55-60 
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    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: An automatic method of obtaining periodic bond chains (p.b.c.) in AaBb compounds is presented. The program analyses every crystallographic short direction and for each it makes systematic trials of every atom succession that could be a p.b.c. The chain is built up with the atoms at the smallest distance from the line considered to be the p.b.c. This program is applied to crystals of rutile, anatase and barite, and it gives all their known p.b.c.'s, plus another two in the case of barite.
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    Acta crystallographica 32 (1976), S. 320-325 
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    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: In order to determine what values of rotational and translational parameters will best allow a large fragment of a protein molecule to explain the diffraction from another protein, a correlation function between Fo and Fc must be defined. Various such correlation functions are discussed; the scalar product ΣFo2(h)Fc2(h) is recommended for establishing the rotation, but the residual is better for the translation. It is shown that the calculation of the latter is not computationally impracticable. A large fragment of the hen-egg-white lysozyme molecule was used as a model for human lysozyme; rotational and translational searches were successful, and the unrefined residual was 49%. Wilson's distribution functions are shown to apply to lysozyme surprisingly well. One consequence of this is that the results of Parthasarathy & Parthasarathi [Acta Cryst. (1972). A28, 426-432] may be used to derive a value of the average error in the coordinates.
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    Acta crystallographica 32 (1976), S. 342-344 
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    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The structure of the triclinic modification of WO3 in terms of the O → W electric dipoles is proposed. In the same way, based on the relationships with the structures of MoO3 and WO2Cl2, the structure of the orthorhombic modification of WO3 is proposed.
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    Acta crystallographica 32 (1976), S. 351-351 
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    [S.l.] : International Union of Crystallography (IUCr)
    Acta crystallographica 32 (1976), S. 351-351 
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    [S.l.] : International Union of Crystallography (IUCr)
    Acta crystallographica 32 (1976), S. 409-411 
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    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The possibility is discussed of applying the theoretical intensity distribution formulae to the structural analysis of solid solution crystals of ZnS-CdS and ZnS-ZnSe with stacking faults. It is pointed out that the irregular shape of the photometric curves, the appearance of intensity maxima connected with areas of disordered type structure, and splitting of the diffuse reflexions, renders impossible the application of theoretical intensity formulae. Theoretical intensity curves, obtained for the model of a structure with stacking faults, are proposed for structural analysis.
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  • 78
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    Acta crystallographica 32 (1976), S. 434-446 
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    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Measurements of lattice parameters and intensities of difference reflexions have been made for all compositions of Nal - xKxNbO3, both at room temperature and above. Structural models are proposed for each phase found.
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    Acta crystallographica 34 (1978), S. 91-94 
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    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The planar bonding in graphite is interpreted in terms of the deformation density approach. The calculated ratio of the 100 and 110 structure factors is in good agreement with experimental results. This suggests possibly a general means of comparing bonding effects in structures where either the strength of the bonding or the atomic environment is similar and where the bonding parameters in one of the structures are known.
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    Acta crystallographica 34 (1978), S. 88-90 
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    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Earlier neutron-diffraction measurements [Willis (1964), Proc. Br. Ceram. Soc. 1, 9-19] on a single crystal of UO2.12 at 800°C showed that interstitial oxygen atoms enter the UO2 lattice at two kinds of site, which are displaced by about 1 Å along the (110) and (111) directions from the cubic-coordinated interstitial sites. It was also shown that the solution of oxygen is accompanied by the formation of vacancies in the normal oxygen sites, but that the uranium sublattice remains undisturbed. A new analysis of the same data has been carried out, which introduces constraints between some of the parameters and allows a more satisfactory treatment of the anharmonic motion of the oxygen atoms. The new analysis leads to a much more precise determination of the occupation numbers of the (110) and (111) oxygen atoms and of the normal oxygen vacancies. The simplest model to account for these new results is the so-called 2:2:2 configuration of oxygen defects.
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    Acta crystallographica 34 (1978), S. 94-102 
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    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The Feynman path-integral formulation of quantum mechanics is used to investigate the theoretical problem of the propagation of high-energy electrons through thin crystalline specimens. The primary objective is to find a satisfactory scattering approximation that accurately describes the transmitted (elastically scattered) wave, and still retains a mathematically invertible relation between the transmitted wave function and the specimen structure. It is shown that the path-integral method leads naturally to an invertible, higher-order, phase-object approximation, in addition to the usual kinematic approximation and the usual phase-object approximation. The higher-order phase-object approximation in turn leads to the noninvertible, multislice approximation of Cowley & Moodie, which had previously been derived by those authors from a semi-classical, physical-optics point of view.
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    Acta crystallographica 32 (1976), S. 504-506 
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    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The 'power method' provides a computationally easy method for the determination of the best plane through a set of points. By repeatedly taking squares, one rapidly obtains the maximum eigenvalue and corresponding eigenvector of the inertia tensor. The result is the least-squares result when the points have independent, isotropic weights.
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    Acta crystallographica 34 (1978), S. 116-120 
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    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Lattice fringes corresponding to (00.3) spacings of the 126R polytype of SiC have been obtained in the electron microscope. A number of 10.l reflections were allowed to pass through the objective aperture to obtain the lattice fringes showing a periodicity of ̃105 Å (one third of the c parameter of the hexagonal cell) and each unit-cell block is subdivided into smaller blocks corresponding to the spacings of 6H, 15R, 21R etc. The stacking sequence of these blocks has been used to work out the detailed structure of the 126R polytype. It has been suggested that the lattice resolution technique in conjunction with X-ray diffraction is likely to prove a useful method for determining difficult polytypic structures.
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    Acta crystallographica 34 (1978), S. 120-123 
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    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: It is shown that a model of growth disorder, describing the way in which substitutional disorder can be introduced into binary solid solutions at growth, exhibits a phase transition. In a particular case it is shown that the distribution in 2D sections of the crystal corresponds to the simple pair-interaction Ising model on a triangular lattice.
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    Acta crystallographica 34 (1978), S. 123-126 
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    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The composition of In3Te4 has been established as a single-phase material. Single crystals of this material have been prepared and its structure has been identified as tetragonal with lattice parameters a0 = b0 = 6.173 and c0 = 12.438 Å. The stability of the structure has also been investigated.
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    Acta crystallographica 34 (1978), S. 127-130 
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    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Bond-length variations within the SiO4 and LiO4 tetrahedra in (Li2SiO3)x are examined in terms of valence-electron population analyses obtained from extended Hückel molecular orbital theory. The results indicate that a significant improvement in the correlations between observed bond length and Mulliken overlap population is obtained when the 'first coordination sphere' of tetrahedral groups is included in the calculations.
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    Acta crystallographica 32 (1976), S. 641-648 
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    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: A simple numerical method of determining the absorption correction factors for spherical and cylindrical specimens is described. The construction of line profiles of the diffraction peaks for both types of specimen illustrates the origin of errors inherent in all numerical methods of this kind. The difference in line profiles, particularly the line shift, for spherical and cylindrical specimens could influence the choice of specimen geometry for accurate lattice parameter determinations.
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    Acta crystallographica 32 (1976), S. 664-666 
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    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Displacive phase transitions and phase transitions of the type disorder-order usually result in symmetry changes such that the space groups of both structures are related as group and subgroup. The subgroups of a space group always belong to one of the following three types: they have either the same primitive cell as the original space group (they are translationengleich), or they belong to the same crystal class (klassengleich), or they are general (allgemein), i.e. they do not belong to either one of the previous categories exclusively and thus have lost translations as well as other symmetry operations with respect to their higher-symmetry (parent) space group. Twin domains are expected whenever the derived structure belongs to a lower-symmetry crystal class. Antiphase domains are possible whenever the derived structure has lost translational symmetry operations. The usefulness of these considerations is demonstrated and discussed for several materials with derivative structures.
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    Acta crystallographica 32 (1976), S. 671-672 
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    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The Darwin difference equations are solved numerically for the case of a crystal having a depth-dependent d spacing.
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    Acta crystallographica 32 (1976), S. 691-745 
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    Acta crystallographica 32 (1976), S. 747-747 
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    Acta crystallographica 32 (1976), S. 749-749 
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    Acta crystallographica 32 (1976), S. 749-750 
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    Acta crystallographica 34 (1978), S. 143-156 
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    Acta crystallographica 34 (1978), S. 142-142 
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    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The reported large discrepancies between the measured and the tabulated absorption coefficients of silicon [Lawrence, Acta Cryst. (1977), A33, 343] are shown to arise from the neglect of the scattering contribution and probably from contamination of the incident beam by harmonic wavelengths.
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    Acta crystallographica 34 (1978), S. 157-157 
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    Acta crystallographica 34 (1978), S. 140-142 
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    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: X-ray measurements of the lattice spacings in three Ag-Ge alloys in the temperature interval 30-595°C and in two Cu-Ge alloys in the temperature interval 25-611°C, in the solid-solution range, have been made with a Unicam 19 cm high-temperature camera. The measured lattice spacings have been found to increase non-linearly with temperature, this non-linearity being slightly enhanced for Cu-9.25 at.% Ge alloy. The dependence of the measured lattice spacings on temperature has been expressed in an analytical form (polynomial of second degree) from least-squares fitting of the data. The thermal expansion coefficient, α, for the alloys considered, in general, has been found to decrease linearly with increasing temperature (from ∼25 to ∼17 × 10-6°C-1), except for the greater germanium concentration (9.25 at.%) in copper solvent where the tendency is reversed.
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    Acta crystallographica 34 (1978), S. 158-158 
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    Acta crystallographica 34 (1978), S. 158-159 
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    Acta crystallographica 34 (1978), S. 159-160 
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