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  • Wiley-Blackwell  (127,217)
  • American Institute of Physics  (101,621)
  • International Union of Crystallography (IUCr)  (17,216)
  • 1980-1984  (78,905)
  • 1975-1979  (69,182)
  • 1965-1969  (56,772)
  • 1960-1964  (41,195)
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  • 1
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics
    ISSN: 1089-7658
    Source: AIP Digital Archive
    Topics: Physics , Electrical Engineering, Measurement and Control Technology
    Notes: Papers in mathematical physics - that is, the application of mathematics to problems in physics and the development of mathematical methods suitable for such applications and for the formulation of physical theories
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  • 2
    Electronic Resource
    Electronic Resource
    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 1 (1968), S. 1-19 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: The desirability and requirements for a specimen capable of testing the resolving power and other image characteristics of an electron microscope are discussed in detail. In this discussion, the underlying diffraction phenomena are particularly utilized. A partially graphitized carbon black is shown to satisfy the requirements extremely well and constitutes an easily prepared specimen for conducting tests of image quality in the molecular size range. The structure of the test object is known in detail with the result that readily interpretable phase contrast images are obtained. Micrographs illustrating the use of the 3.4 Å (002) spacing for magnification calibration, astigmatism and asymmetry check as well as resolving power are exhibited. The second order c-spacing of 1.7 Å is occasionally found in an image. The micrographs shown herein were taken with two different electron microscopes by different operators obtaining the same structural detail in the images. It is concluded that the carbon black test object offers the best possibilities for evaluating image performance of any specimen yet suggested.
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  • 3
    Electronic Resource
    Electronic Resource
    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 1 (1968), S. 84-90 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: Bent-glass mirrors can be used to produce a narrow, highly collimated X-ray beam, particularly suitable for photographing diffraction patterns from crystals with very large unit cells (i.e., several hundred Å to a side). A camera is described that employs double-mirror focusing optics with a precession apparatus. A comparison of optical reflection and simple collimation shows that for high resolving power, focusing devices are very much superior to pinhole collimators. The reduction of background is especially noteworthy. Use of this camera has permitted the collection of accurate three-dimensional data from crystals of tomato bushy stunt virus.
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  • 4
    Electronic Resource
    Electronic Resource
    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 1 (1968), S. 121-122 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: A new method for determination of the polarization factor of a crystal monochromator is presented. This method is based on the use of polarized X-rays produced by anomalous transmission or the Borrmann effect. The polarization factors of two quartz (10\overline 11) monochromators of Johansson type have been measured with Cu Kα radiation, and the resulting values are in close agreement with the expression derived from the kinematic diffraction theory.
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  • 5
    Electronic Resource
    Electronic Resource
    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 1 (1968), S. 126-128 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: An adapter which supports a Polaroid flat-plate film holder has been designed for a standard Weissenberg goniometer. A number of applications, including a method for rapidly aligning single crystals, are described.
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  • 6
    Electronic Resource
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 1 (1968), S. 145-153 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: The use of X-ray diffraction topography to identify domains of different polytype in crystals of silicon carbide has been described in a previous paper. Further methods have been developed and applied to the analysis of thin films deposited epitaxically from the vapour phase onto basal surfaces of crystals of hexagonal α-SiC. The epitaxic films consist either of α-SiC, or of the cubic form β-SiC, with multiple twinning about the axis normal to the surface. The fine scale texture of interlocking twin domains is readily demonstrated in X-ray diffraction topographs.
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  • 7
    Electronic Resource
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 1 (1968), S. 165-171 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: Inversion twin boundaries in BeO crystals (wurtzite structure) can be studied by X-ray topography. They can be regarded as a special kind of stacking fault. The section topograph images of a twin boundary, lying parallel to the c axis, agree well with the theory for a single stacking fault. From the contrast variation of the images for various reflections, it is concluded that the oxygen sublattice on one side of the twin boundary is displaced from that on the other side by \mid(1/16)[001]\mid so that the oxygen layer parallel to the basal plane on one side is located at the center of the oxygen and beryllium layers on the other side. The image contrast in section topographs is very sensitive to the phase shift due to a fault. The phase shift of a few degrees can be detected easily. This sensitivity leads to an accurate structure determination of the inversion twin boundary.
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  • 8
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 1 (1968), S. 181-184 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: The refractive index, n, for X-rays is measured by interposing a prism in the path of X-rays falling on a perfect silicon crystal at the Bragg incidence angle. Owing to the deviation angle of the prism, the separation of the two wave fields excited in the silicon crystal is modified, from which the value of n − 1 can be deduced with a 1% accuracy. The method has been applied to the measurement of the anomalous dispersion correction for the refractive index of zirconium for Mo Kα.
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  • 9
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 1 (1968), S. 187-189 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: A method based on the variation of the lattice parameter with Li content, for the quantitative determination of lithium in the system Lix+Ni1−2x2+Nix3+O2−, is proposed. A precision between 1 and 5% relative, depending upon the concentration range, has been obtained. The results are compared with those obtained by flame emission spectroscopy. For values of x 〉 0.12 the original rhombohedral lattice transforms into a face centred cubic lattice.
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  • 10
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 1 (1968), S. 198-198 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
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  • 11
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 1 (1968), S. 139-145 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: A study of strain inhomogeneities in a zone-refined tungsten crystal oriented for (123) slip was carried out before and after a slight compression. The study was based on changes of interplanar spacings measured along different crystallographic directions and samples from different areas of the crystal by means of the X-ray back-reflection divergent beam method. Upon compression a redistribution of the locked-in elastic strains took place and the induced strains assumed a more homogeneous distribution for one of the sets of (123) planes considered. This homogeneity in the strain distribution along definite crystallographic directions is believed to result from the interaction of the primary slip dislocations with the pre-existing dislocation configuration and appears to be characteristic of the initial stage of work-hardening. The dislocation interaction induced by a small strain found practical application in the elimination of a troublesome substructure in highly zone-refined tungsten crystals and appears to form the scientific basis of certain stress-relief treatments long practised in metallurgical technology.
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  • 12
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 1 (1968), S. 218-226 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: All the hard carbons are composed of three phases when they are heated above 2000°C: non-graphitizable carbon, graphitizable carbon, and graphite (the latter two appearing only in very small amounts). When the heat treatment temperature is increased to 3000°C, these phases change in various ways. At low temperatures, the non-graphitizable phase is formed by small turbostratic stacks of carbon layers which are oriented completely at random inside the carbon grains. Above 2000°, these stacks begin to undergo mutual rearrangement to produce small fibers by ordering roughly parallel to each other. The graphitizable phase is formed of spheres made up of conical rolled spirals, which are themselves made up by turbostratic stacking of the carbon layers. When heat treated, each sphere transforms to graphite very suddenly. The third phase is well crystallized graphite with stacking faults and twist defects.
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  • 13
    Electronic Resource
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 1 (1968), S. 241-246 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: Samples in the Bi–Te system containing 59.0, 58.0, 57.0, 55.0, 51.0, and 50.0 at.% Te, in addition to 5 samples within the Bi2Te3 homogeneity range, have been equilibrated near 525 or 450°C and room temperature powder diffraction patterns taken. There are now 4 known phases in the 50–60 at.% Te region. The 59.0 and 58.0 at.% samples are two phase at 525°C. The 57.0 and 55.0 at.% samples are new phases with hexagonal parameters, a = 4.4106±0.0002 Å, c = 54.330±0.003 Å and a = 4.4214±0.0004 Å, c = 78.195±0.012 Å, respectively. The 51.0 and 50.0 at.% samples are two-phase at 525 C. At 450°C the 51.0 at.% sample is single phase while the 50.0 at.% sample probably is not. The common indexing scheme for the 50.0 and 51.0 at.% samples is different from those for the 55–0 and 57.0 at.% samples. For the 51.0 at.% sample a = 4.4296±0.0002 Å and c = 24.017±0.001 Å. The 00l lines for all these phases vary strongly with composition and those near d = 9 and 5 Å are isolated enough to provide a convenient way of distinguishing among the various phases. The results are discussed in terms of other phase-diagram information. They are inconsistent with Stasova's correlation between composition and powder-pattern indices for the Bi–Te, Bi–Se, and Sb–Te systems.
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  • 14
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 1 (1968), S. 262-262 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
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  • 15
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 1 (1968), S. 263-271 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: The study of the scattering outside the Bragg reflexions shows no local order in the ordered phase I of alloys such as Au (50 at. %) Cu (46 at. %) Ni (4 at. %) even for the smallest degree of long range order. The modulation of the scattering appears only with the presence of short range order in the disordered α phase. There is evidence of a two-phase region on the equilibrium diagram at the AuCu3 stoichiometric composition.
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  • 16
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 1 (1968), S. 290-292 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: Accurate lattice parameters (at 25 and 48°C), density, thermal expansion coefficients, the indexed powder pattern, and optical data are given for Ba(4+x)Na(2−2x)Nb10O30, where x = 0.13±0.013, grown by pulling from a nominally stoichiometric melt.
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  • 17
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 1 (1968), S. 313-317 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: In an earlier communication by the authors it was shown that the stack height distribution in a raw carbon black followed an exponential law. Extension of these studies to a heat-treated (2000°C) black showed that the exponential law is still valid when stacking is extensive. The exponential law and the effect of heat-treatment are explained by the existence in blacks of extensive stratification rather than the presence of short stacks of small layers. Evidently heat-treatment results in annealing of the strata to yield uniform layer domains and more ordered stacking. Simple expressions are derived for calculating the profiles of the 00l reflections and the coefficient of the exponent.
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  • 18
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 1 (1968), S. 324-325 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
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  • 19
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 1 (1968), S. 323-323 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: Long chain secondary ammonium chlorides, bromides and iodides crystallize in a preferred orientation. Values of the basal spacings of the salts indicate hydrocarbon chains oriented towards each other between planes of the ionic heads. The inclination angle of the chains was found to be 40°.
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  • 20
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 2 (1969), S. 72-76 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: The paper describes a method for obtaining consistent estimates of domain size from an evaluation of coefficients derived from curves fitted to the tails of diffraction profiles. An estimate of the mean domain size is computed directly from the intensity data and this is equivalent to the value derived from the slope of the variance-range function. For many applications this provides a convenient alternative to the method described by Langford & Wilson (Crystallography and Crystal Perfection. London: Academic Press, 1963) but does not replace it. An advantage of the present method is its simplicity and consequent reduction in computing time. It is easier to apply if a computer is not available and is applicable in cases where one or other of the profile tails overlaps that of a neighbouring line. The results obtained by this method are comparable in accuracy to those given by existing techniques.
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  • 21
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 2 (1969), S. 18-24 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: The usual method of specimen preparation for electron-probe microanalysis can introduce errors of up to about ±3% in the estimates of the amount of an element present. It is believed that these errors are caused by the formation of `flowed' layers on the surfaces of polished samples. Two methods of reducing the errors are described.
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  • 22
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 2 (1969), S. 30-36 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: The lattice constants and the atomic position parameter, z, of a high purity, low strain, single-crystal of arsenic have been determined. Low extinction reflections of filtered Mo Kα and Ag Kα radiation were used for the determination of z. The Bond precision technique with Mo Kα radiation was used for the determination of the unit-cell dimensions a and c. Average values for a and c in Å, and for z are: 4.2°K z = 0.22764 a = 3.7597 c = 10.4412; 78°K z = 0.22754 a = 3.7595 c = 10.4573; 299±3°K z = 0.22707 a = 3.7598 c = 10.5475. The estimated standard deviation of z is ±0.00004 at 4.2°K, ±0.00002 at 78°K and ±0.00005 at 299°K. The precision of a is estimated to be ±0–0001 Å and that for c to be ±0.0002 Å. The results for As are compared with those reported earlier for Sb and Bi.
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  • 23
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 2 (1969), S. 146-147 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
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  • 24
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 2 (1969), S. 156-164 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: The strain induced phase transformations produced in lead monoxide powders by ball milling at temperatures ranging from −196 to 200°C have been studied by X-ray diffraction methods. It has been found that either of the two polymorphs, litharge and massicot, was partially converted to the other at all the temperatures investigated, and that, whichever polymorph was the starting material, the end product, after a sufficiently long time, was a mixture of the two polymorphs, both highly strained. The percentage of each phase present was found to be dependent on the temperature of deformation. The results have been interpreted by consideration of the production of the microstrain energy required to overcome the energy barrier to the transformation, and of the shear generated in the mill on the pressure-temperature phase diagram. It is considered that shear stresses can affect the nature of the pressure-temperature phase diagram, in a manner theoretically postulated by Kumazawa. The commercial importance of the results has been briefly outlined.
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  • 25
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 2 (1969), S. 176-180 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: The theory of the direct comparison X-ray method of phase analysis is extended to correct for preferred orientation effects. Texture parameters are defined to assess the type and intensity of preferred orientation using data from diffractometer patterns. The analysis is illustrated with results obtained on three austenitic stainless steels.
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  • 26
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 2 (1969), S. 192-192 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
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  • 27
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 2 (1969), S. 200-209 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: A method is presented which combines the analysis of X-ray absorption profiles and selected area X-ray topographs. The method is based on X-ray divergent beam patterns obtained in transmission. The absorption profiles are obtained by unfolding the spectral distribution from the profiles of the deficiency conics, whereas the selected area topographs derive from the corresponding diffraction conics. The synergy of the two techniques makes the method particularly useful for the elucidation of anisotropic effects and inhomogeneities of defect structures. An example is given for the room temperature deformation of beryllium.
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  • 28
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 2 (1969), S. 223-230 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: An X-ray reflexion topography camera has been designed to study structural defects near the surface of monocrystalline semiconductors. Large surfaces can be covered by means of successive fixed exposures. A surface of 30 mm x 10 mm for example can be studied in less than ten minutes on nuclear emulsions. The conditions for the observations of dislocations in gallium arsenide have been examined: the choice of reflecting planes is limited by the depth of penetration of X-rays, so that the effective crystal thickness must be of the order of the width of a dislocation image (2-5 microns). Studies to which these observations can be applied are numerous: structural defects induced by diffusion, lattice strains, orientation of dislocations near the surface, structural evolution of silicon during integrated circuits elaboration, structure of cleavage surfaces, lapping and polishing defects, structural defects of epitaxic layers.
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  • 29
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 2 (1969), S. 234-234 
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  • 30
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 2 (1969), S. 236-236 
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  • 31
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 2 (1969), S. 249-252 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: The practical importance of tungsten monocarbide prompted an investigation into its wear mechanism. Initial studies on ball-milled tungsten carbide powders revealed considerable plastic deformation, coupled with a reduction in crystallite size. Deformation stacking faults, involving slip on the basal plane, were observed. The work was extended to sintered blocks, tool tips and single crystals. Studies on the worn surfaces of these revealed plastic deformation that extended to a depth of a few microns below the surface. The plastic deformation is an important factor in the wear of tungsten carbide.
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  • 32
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 2 (1969), S. 295-297 
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    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: A method is suggested which allows several independent determinations of the rhombohedral angle using data from a single diffraction pattern. This is applied to the intermetallic compound SbSn.
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  • 33
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 2 (1969), S. 297-300 
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    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: The Hankel transform method proposed by Fedorov & Aleshin (1966; Vysokomol. Soed. 8, 1506; English translation, 1967: Polymer Science USSR 8, 1657) for calculating the electron density of long cylindrical particles with circular cross section is tested with theoretical intensity functions for which the density can be found both by an exact calculation and by numerical integration. (In this method, the density is assumed to depend only on the distance from the cylinder axis.) The tests show how the degree of resolution obtained in the density curve is related to the largest scattering angle at which data are available. For the step function density corresponding to a cylinder with uniform electron density, the requirements are more severe than for continuously decreasing density functions. The possibility of obtaining useful results with the available scattering data from two biological macromolecules is discussed.
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  • 34
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 2 (1969), S. 247-248 
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    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: A previously given analysis of the beam and specimen tilt errors in the Bond single-crystal method of lattice parameter determinations is extended to give a simple generalized treatment. This shows that the error passes through a maximum in accordance with an empirical observation by other workers. Crystal alignment procedures are examined in the light of the results.
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  • 35
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 2 (1969), S. 259-261 
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    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: A storage oscilloscope has been attached to the IBM 1800 computer that is used for pole-figure data acquisition. It allows fast plotting of pole figures by modulation of the cathode ray beam according to the pole density as it scans the stereographic projection along a spiral path. The time needed to plot the pole figure is reduced by a factor of eight as compared with a mechanical plotter.
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  • 36
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 2 (1969), S. 281-288 
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    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
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    Notes: The axial thermal expansion of monoclinic and tetragonal ZrO2 and of monoclinic HfO2 was studied over the temperature range from room temperature to 1400 °C. The linear thermal expansion coefficients were calculated. Thermal expansion along (x 106 per °C) a = 10.31 monoclinic ZrO2, 11.60 tetragonal ZrO2, 9.34 monoclinic HfO2; b = 1.35 monoclinic ZrO2, – tetragonal ZrO2, 2.98 monoclinic HfO2; c = 14.68 monoclinic ZrO2, 16.08 tetragonal ZrO2, 13.10 monoclinic HfO2. Some aspects of the present study, such as anisotropy of thermal expansion and a pretransformation vibrational anomaly, are discussed briefly.
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    Applied crystallography online 8 (1975), S. 29-36 
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    Notes: A stereographic projection method of analysis has been developed for analyzing the misorientation contrast of crystal subgrain boundaries which are observed in Berg–Barrett X-ray micrographs. The boundary appearance is described in terms of the geometry of the boundary with respect to the crystal surface, the angular misorientation of the adjacent subgrains, and the X-ray diffraction conditions. The rotation axis for the misorientation of adjacent subgrains, including the sense of the rotation, and the amount of misorientation is determined from the width and relative contrast of the boundary in various images. Experimental results are described for subgrain boundaries in zinc crystals solidified along different crystallographic growth directions. The Burgers vectors of the dislocations composing the subgrain boundary are indirectly determined by this method.
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  • 38
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    Applied crystallography online 8 (1975), S. 42-44 
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    Notes: A means of measuring strain and lattice parameter directly in epitaxic layers by `double-crystal' X-ray diffraction is presented. The method described has three major advantages; that it is achieved by a simple addition to a commercial goniometer; that the area of sample illuminated is defined solely by the collimator; and that single or double-crystal diffraction can be selected, simultaneously if needed, on exactly the same specimen area.
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  • 39
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    Applied crystallography online 8 (1975), S. 45-48 
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    Notes: A silicon powder Standard Reference Material, SRM-640, has been prepared for use as a standard in powder diffractometry. Powder diffraction measurements were performed with a tungsten internal standard and a high-angle goniometer. The measured a/λ is 3.525176. With λ(Cu Kα1 peak) taken as 1.5405981 Å, a = 5.430880 (35) Å, uncorrected for refraction. Comparison of a with values obtained with a single-crystal from one of the boules reveals a difference of 3 parts in 105. This difference suggests a subtle systematic error in powder diffractometry or a change in lattice spacing near crystal boundaries. Use of the SRM should permit individual measurements of lattice parameters to be made reproducible to near 1 part in 105 and an absolute accuracy of at least 3 parts in 105.
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  • 40
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    Applied crystallography online 8 (1975), S. 111-114 
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    Topics: Geosciences , Physics
    Notes: The assumptions in the Borie & Sparks [Acta Cryst. (1971). A27, 198–201] procedure for the separation of order- and displacement-dependent components of diffuse X-ray scattering from a binary system AB are examined with the use of the concentration deviation (spin-like) notation. The more limiting assumption, that the structure-factor ratio η = (mAfA + mBfB)/(fA−fB) is constant in reciprocal space, is shown to produce an incomplete separation for normal variations in η. A matrix-inversion method for completing the separation is suggested for those cases in which the approximate equality of the Debye–Waller factors (DWF) of the individual atomic species indicates that some terms of the scattering equation may be neglected. The extension suggested by Ramesh & Ramaseshan [Acta Cryst. (1971). A27, 569–572] that anomalous dispersion induced changes in η could be used to separate the atomic static displacement properties of the various atomic pairs is shown to require a change in η greater than the variation of η across the reciprocal-space volume. Some difficulties of obtaining such a change are pointed out.
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  • 41
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    Applied crystallography online 8 (1975), S. 121-126 
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    Notes: The role of positional information in determining the thermodynamics of crystalline solid solutions is considered. It is noted that, with certain exceptions (e.g.b.c.c. Fe–B), such solutions can be classified as being exclusively either substitutional or interstitial with respect to each solute. Calculation of thermodynamic properties of intersitital solutions requires knowledge of the types of sites preferentially occupied by the solute. The problem of determining that occupancy is considered for several binary systems. A cumulant expansion technique, which meets with good success in describing dilute, high-temperature, interstitial solutions, is applied to the case of high-temperature binary substitutional systems of similar metals. The technique is shown to be of limited utility in this application.
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  • 42
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    Applied crystallography online 8 (1975), S. 127-127 
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    Notes: It may be essential in certain cases (e.g. non-dilute alloys and dislocations) to take into account the (pair and higher-order) correlations in the defect distribution. To this end the kinematic expression for the total scattered intensity is rewritten.
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    Applied crystallography online 8 (1975), S. 132-132 
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    Notes: If the occurrence of one or two-dimensional local order in alloys or in neutron-irradiated materials has been known for many years, the observation by X-ray and neutron scattering of quasi-one-dimensional order due to displacements or correlated motions of atoms along independent chains is more recent. Examples to be discussed are given.
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    Applied crystallography online 8 (1975), S. 75-75 
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    Applied crystallography online 8 (1975), S. 76-76 
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    Applied crystallography online 8 (1975), S. 128-128 
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    Notes: Structural studies showed that oxygen atoms in Ih ice are well ordered whereas hydrogen atoms are `statistically' distributed on two possible sites on each O–H–O bond.
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    Applied crystallography online 8 (1975), S. 185-185 
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    Notes: The integral Huang diffuse X-ray scattering from crystals containing small dislocation loops can be analyzed to obtain two types of information: (1) the size distribution of the loops and (2) the total number of point defects contained in the loops. This technique has been applied to copper crystals irradiated under a number of conditions of neutron irradiation flux, dose and temperature, for which loops are produced, and to selected annealing studies of these loops, with all X-ray measurements made at room temperature.
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  • 48
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    Applied crystallography online 8 (1975), S. 191-192 
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    Topics: Geosciences , Physics
    Notes: Explanations for the broadening of X-ray line profiles of plastically deformed crystals in terms of the density and the distribution of the dislocations introduced during deformation are given.
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    Applied crystallography online 8 (1975), S. 140-140 
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    Notes: The ω phase transformation in Zr–Nb alloys has been studied by measuring the X-ray diffuse scattering in the (110) plane and the Mössbauer diffuse scattering along the 〈111〉 direction of separate single crystals with compositions ranging from 8 to 30% Nb.
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    Applied crystallography online 8 (1975), S. 141-141 
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    Notes: A simple crystallographic approach in obtaining the final martensitic structure [3R, 1R, 2H) from the initial displacive modes is presented.
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    Applied crystallography online 8 (1975), S. 142-142 
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    Notes: The theory of the diffuse scattering from crystals with small concentrations of point defects and small clusters is reviewed.
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    Applied crystallography online 8 (1975), S. 143-143 
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    Notes: Analytic expressions for the dilation and the stress tensor in reciprocal space are discussed.
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    Applied crystallography online 8 (1975), S. 203-203 
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    Notes: The boundary between the −X and Z growth regions in synthetic quartz has been studied using X-ray topography and other techniques and it has been found that the crystal lattice remains coherent at the boundary.
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    Applied crystallography online 8 (1975), S. 204-204 
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    Notes: The diffraction of electrons is, in principle, a very sensitive probe of the relative atomic positions in ordered or disordered crystals. The full potential of electron diffraction and electron microscopy methods for the study of local atomic arrangements has not been realised because of the difficulties of conducting experiments under sufficiently well defined conditions and because of the complications introduced by the dynamical diffraction processes involved.
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    Applied crystallography online 8 (1975), S. 183-183 
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    Notes: The diffuse elastic neutron scattering due to distortion of the Pb host lattice around Bi substitutional atoms has been measured at the HFR in Grenoble and the results discussed.
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    Applied crystallography online 8 (1975), S. 175-183 
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    Notes: For interstitials the scattering cross section between the Bragg reflections is very sensitive to the position of the defect atom and the displacements of the neighbouring lattice atoms. In contrast to this the scattering near the Bragg reflections (Huang scattering) is mainly governed by the displacement field at large distances from the defect and gives information about defect symmetry and strength [Trinkaus, H. (1972). Phys. Stat. Sol. (b) 51, 307–319]. For determining structures of point defects a measurement of scattering far from reciprocal-lattice points is therefore the best suited and most direct method. X-ray measurements of point-defect scattering in this region far from reciprocal-lattice points are difficult. With conventional X-ray set-ups it is not possible to separate the defect scattering from the thermal diffuse and Compton background scattering which is up to two orders of magnitude larger in the case of typical defect concentrations of some 10−4. Such measurements, however, become possible if large X-ray sources of high luminous density are used in connexion with multidetector arrangements. As an example an experimental arrangement [Haubold, H.-G. & Schilling, W. (1975). To be published; Haubold, H.-G. (1974). Rep. Kernforschungsanlage Jülich, JUL-1090-FF] is reviewed, in which the scattering cross-section of self-interstitials in aluminium was measured in samples containing an atomic density of interstitials up to 5 × 10−4.
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    Applied crystallography online 8 (1975), S. 184-184 
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    Notes: Second-order pseudopotential calculations are known to reproduce fairly well the structure and phonon spectra of many simple metals. The validity of the underlying assumption of linear screening for impurities with valences and core radii close to those of the host can be checked a posteriori and by comparing calculated properties with measurements on dilute alloys, and, especially, coherent elastic neutron scattering.
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    Applied crystallography online 8 (1975), S. 185-185 
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    Notes: Analytical methods to describe the scattering from crystals containing defect clusters with strong displacement fields are reviewed.
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    Applied crystallography online 8 (1975), S. 193-194 
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    Notes: Work which has been started at Pelindaba on small-angle scattering in neutron irradiated copper is described.
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    Applied crystallography online 8 (1975), S. 193-193 
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    Notes: Voids formed in neutron irradiated metals are faceted on various crystallographic planes. This faceting has been shown to cause significant anisotropy in the small-angle scattering pattern. It is shown that it is possible to obtain the specific void surface energies from small-angle diffuse scattering data.
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    Applied crystallography online 8 (1975), S. 224-224 
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    Notes: The weak-beam method of electron microscopy provides a means for studying lattice defects with greatly increased resolution compared with normal diffraction contrast techniques.
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    Applied crystallography online 8 (1975), S. 386-387 
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    Notes: The thermal expansion of cyclopentadienylthallium, TlC5H5, was determined in the range 78 to 295 K, using X-ray powder diffractometry. Expansion is very anisotropic: α1 = 125 ± 12, α2 = 97 ± 5, α3 = 0 ± 4 (all 10−6 K−1). Directions and ratio of the two greatest expansion coefficients: α1 and α2, are explained by considering the shortest distances Tl+–Tl|+ in this ionic structure.
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    Applied crystallography online 8 (1975), S. 392-395 
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    Notes: Several guanidinium salts have been studied since, because they contain six hydrogen atoms per unit charge, they are likely to contain multiple hydrogen bonding systems [see e.g. Adams & Small (1974). Acta Cryst. B30, 2191–2193], which are of interest in themselves and are also likely to cause stabilization of the structure. The crystal data of a range of salts were collected and are given. Space group and approximate cell dimensions were obtained from oscillation and Weissenberg photographs. Powder diffraction data [0° to 60° (2&thgr; using Cu Kα)] were indexed and the cell parameters refined using the programs PIRUM of Werner [Program No. 1, World List of Crystallographic Computer Programs (3rd. ed.): J. Appl. Cryst. (1973). 6, 309–346] and CELFIT of Bracher [UKAEA Research Report, AERE-R5412 (1967)].
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    Applied crystallography online 8 (1975), S. 397-397 
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    Notes: Unlike the position with negatively charged substituents, little has been done on benzaldehydes ortho-substituted with positively charged groups. This is more especially true in the field of crystallography where only the X-ray and neutron diffraction study of o-nitrobenzaldehyde has been reported [Coppens & Schmidt, Acta Cryst. (1964). 17, 222–228; Coppens, Acta Cryst. (1964). 17, 573–578]. Preliminary results of a structural investigation on Se- and Te-containing benzaldehydes are presented. The main purpose is to corroborate and to complete the conclusion of recent n.m.r. work on the conformation of these molecules [Baiwir, Llabres, Denoel & Piette, Mol. Phys. (1973). 25, 1–7]. The following compounds have been studied: C6H4.COH.TeCl, C6H4.COH.TeBr, C6H4.COH.TeI, C6H4 COH.SeCl, C6H4.COH.SeBr. The crystal structure of the second (TeBr) has been recently reported [Baiwir Llabres, Dideberg, Dupont & Piette, Acta Cryst. (1974). B30, 139–143] and the structure of the last (SeBr) is presently in the final stage of refinement.
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    Applied crystallography online 8 (1975), S. 402-402 
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    Applied crystallography online 8 (1975), S. 403-403 
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    Applied crystallography online 8 (1975), S. 405-414 
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    Notes: Quantitative liquid-structure analysis using energy-scanning diffraction rather than the traditional angle-scanning diffraction is introduced. In the experimental method, white radiation and a solid-state detector are employed. This new method is inherently faster and less beset with problems of experimental instability than are angular-scanning methods. However, many differences in analysis are introduced. In particular, measurement of the primary beam spectrum, the nature of the absorption and dispersion corrections, details of the polarization correction, the ranges of the atomic scattering factor and of the incoherent scattering term, and the mating of different scattering regimes all require special consideration. Application of the new instrumental method and the reconstructed analytical procedure to liquid mercury at room temperature has produced a result in agreement with other recent studies.
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    Applied crystallography online 8 (1975), S. 421-429 
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    Notes: A new small-angle X-ray scattering facility which utilizes a 6 kW rotating anode, pin-hole collimation, and a position-sensitive proportional counter has been developed. As presently constructed, the minimum scattering vector κ (= 4π sin &thgr;/2) which can be reached with Cu Kα radiation is 5 × 10−3 Å−1. Under these conditions the flux incident on the specimen has been found to be 6 × 105 photons s−1. The system has several advantages compared with traditional long-slit geometries; namely, (i) it can quantitatively measure anisotropic scattering distributions, (ii) it avoids large mathematical corrections of the data for slit-smearing effects, and (iii) it minimizes double Bragg scattering in crystalline materials and multiple diffuse scattering in amorphous or liquid materials. To illustrate the performance of this instrument, the scattering curves obtained from four widely different samples are shown. These are: polyethylene, a neutron-irradiated aluminium single-crystal containing voids, a dilute suspension of Ludox spheres, and duck tendon collagen. Quantitative comparisons of the performance with a Kratky camera and with the neutron small-angle scattering facility in Jülich are given.
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    Applied crystallography online 8 (1975), S. 457-458 
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    Notes: The lattice constants of a diamond platelet and of large single, undoped, crystals of silicon and germanium have been determined from measurements of multiple diffraction patterns by the method described in Part I [Post (1975). J. Appl. Cryst. 8, 452–456]. The mean values, based on measurements of eight to twelve reflections, and their standard deviations are: diamond a = 3.566986 Å, Aa/a = 2.6 × 10−6; silicon a = 5.430941 Å, Aa/a = 2 × 10−6; germanium a = 5.657820 Å, Δa/a = 1.6 × 10−6.
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    Applied crystallography online 8 (1975), S. 469-472 
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    Notes: The Mn3+ site distribution in a manganese-containing tsilaisite tourmaline sample has been determined as 46±3 wt. % in the larger Y octahedral sites and 54± 3 wt. % in the smaller Z octahedral sites. For this, a novel application of anomalous X-ray scattering techniques, in conjunction with the energy dispersive X-ray diffraction procedure, has been used. This method appears to be versatile and applicable to many different elements.
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    Applied crystallography online 8 (1975), S. 491-492 
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    Notes: An inexpensive calculation is outlined for determining those reflexions suffering large absorption errors, and for correcting those with smaller errors.
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    Applied crystallography online 8 (1975), S. 496-496 
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    Applied crystallography online 8 (1975), S. 496-497 
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    Applied crystallography online 8 (1975), S. 375-379 
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    Notes: The lattice parameters and the linear coefficient of the lattice thermal expansion of f.c.c. β-Cu2−xSe (1.86 ≥ 2−x ≥ 1.72) were determined by means of the Debye–Scherrer X-ray diffraction technique in the temperature range 25–336°C. The concentration and temperature dependence of the coefficient of thermal expansion are discussed. In addition the equilibrium phase diagram of the Cu–Se system in the region of a non-stoichiometric Cu2−xSe compound (2.00 ≥2−x ≥1.72) was redetermined, with special consideration of the homogeneity range of the f.c.c. β-Cu2−xSe, and compared with previously published results.
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  • 75
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    Applied crystallography online 8 (1975), S. 391-391 
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    Topics: Geosciences , Physics
    Notes: Crystals of Tl2GeS3 were grown by solidification from melts. The compound is triclinic with lattice parameters a = 8.06, b = 12.70, c = 6.76 Å, α = 96°39′, β = 93°10′, γ = 99°31′. Powder data are given.
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  • 76
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    Applied crystallography online 8 (1975), S. 589-597 
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    Topics: Geosciences , Physics
    Notes: A computer program has been written in Fortran for the numerical calculation, using generalized spherical harmonics, of the texture of a sample, even when it has no symmetry. Automatically plotted pole figures, corrected and normalized, make it possible to begin to control the results. Reconstituted pole figures are plotted as a function of Cmνl. The calculations, based on the theoretical developments of Bunge [Mathematische Methoden der Texturanalyse. (1969). Berlin: Akademie Verlag] were carried out with different numerical analyses so as to reduce the size of the calculation and the time taken.
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  • 77
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    Applied crystallography online 8 (1975), S. 578-581 
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    Topics: Geosciences , Physics
    Notes: The white X-ray diffraction method with the use of a powder sample [Laine, Läihteenmäki & Kantola (1972). X-ray Spectrosc. 1, 93–98] was improved by paying special attention to the following four points: (i) the determination of the energy spectrum of incident white X-rays, (ii) the measurement of the energy dependence of the relative absorption coefficient, (iii) the correction for the contribution from thermal diffuse scattering, and (iv) the correction for the anomalous dispersion. The determination of the structure factors of GaP is shown as an example of its applications. The structure factors determined were compared with those obtained by the usual angle dispersive method with monochromated X-rays on the same sample. It is shown that these two sets of structure factors mostly agree within the limit of reproducibility.
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  • 78
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    Applied crystallography online 8 (1975), S. 612-614 
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    Notes: The errors in the Fourier coefficients of the α1 component obtained by α2 elimination are investigated analytically. The effects of counting statistics, of an incorrect intensity ratio of the α1 and α2 components and of an incorrect doublet separation are calculated. The mean-square error in the Fourier coefficient caused by counting statistics is a periodic function of the harmonic number, while errors in the intensity ratio and in the doublet separation primarily affect the first Fourier coefficients. The results are confirmed by computer simulations and by computations with experimental line profiles. The α2 elimination methods assume a perfect shape identity of the α1 and α2 components, but this assumption is not completely justified. Deviations might be interpreted as local errors in the doublet separation and the intensity ratio.
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  • 79
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    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 8 (1975), S. 628-635 
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    Topics: Geosciences , Physics
    Notes: The textures of undirectionally and reversed rolled aluminium sheets were measured using thermal neutrons and Cu and Mo Kα radiation. The samples for the X-ray measurements were prepared in three different ways so that the degree of correspondence between textures as measured with neutrons and X-rays could be investigated. It is shown that agreement can be achieved if the X-rays used penetrate sufficiently into the sample and if a composite type sample is used.
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  • 80
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    Applied crystallography online 9 (1976), S. 14-17 
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    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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  • 81
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    Applied crystallography online 9 (1976), S. 34-38 
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    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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  • 82
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    Applied crystallography online 9 (1976), S. 253-254 
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    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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  • 83
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    Applied crystallography online 9 (1976), S. 257-258 
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  • 84
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    Applied crystallography online 9 (1976), S. 286-290 
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    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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  • 85
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    Applied crystallography online 11 (1978), S. 73-79 
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    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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  • 86
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    Applied crystallography online 11 (1978), S. 114-120 
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    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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  • 87
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    Applied crystallography online 11 (1978), S. 102-113 
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    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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  • 88
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    Applied crystallography online 11 (1978), S. 137-140 
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    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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  • 89
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    Applied crystallography online 11 (1978), S. 148-150 
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    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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  • 90
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    Applied crystallography online 9 (1976), S. 254-256 
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    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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  • 91
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    Applied crystallography online 9 (1976), S. 258-258 
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  • 92
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    Applied crystallography online 11 (1978), S. 157-158 
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    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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  • 93
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    Applied crystallography online 9 (1976), S. 507-508 
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    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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  • 94
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    Applied crystallography online 9 (1976), S. 361-364 
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    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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  • 95
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    Applied crystallography online 9 (1976), S. 369-370 
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  • 96
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    Applied crystallography online 10 (1977), S. 32-36 
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    Notes: The dielectric constants (εr) of several cadmium iodide polytypes have been measured and found to be higher than that of the parent 4H structure. The dielectric constants for several long-period polytypes have been found to lie between 60 and 190 whereas the 4H parent structure has a value in the range of about 15 to 30. In particular, both increasing polytype periodicity and increasing disorder increase the dielectric constant, e.g. from 16 for an ordered 4H structure to 114 for a 32H structure and 67 for a highly disordered 4H structure. In the absence of disorder a particular polytype has its own characteristic dielectric constant value, e.g. the two 14H polytypes which have a common εr value of 63.
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    Applied crystallography online 10 (1977), S. 57-59 
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    Notes: The separation or overlapping of adjacent subgrain images in Berg–Barrett X-ray (reflection) micrographs is described for a reasonably general misorientation between the crystal subgrains. The five crystallographic parameters which describe the diffraction experiment also specify, effectively, the direction of the rotation axis for the misorientation, the amount of the angular misorientation, and the relative orientation of the subgrain boundary interface.
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    Applied crystallography online 10 (1977), S. 62-63 
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    Notes: An effective method for greatly reducing the electron exposure of radiation-sensitive organic or biological specimens while recording their diffraction patterns in a high-voltage (MeV range) electron microscope is described. It involves recording on double-coated screen-type medical X-ray film and backing it with a luminescent radiographic screen which intercepts the transmitted electrons and emits visible light that exposes the bottom emulsion of the film. Values of sensitivity, resolution, and enhancement ratio are tabulated: the latter values range up to 41. Typical patterns taken with l-valine are shown.
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    Applied crystallography online 9 (1976), S. 415-416 
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    Applied crystallography online 9 (1976), S. 417-417 
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