Standard Data for the Identification of Phases By X-Ray Diffraction

1973 ◽  
Vol 17 ◽  
pp. 20-31
Author(s):  
Howard F. McMurdie

AbstractThe identification of crystalline phases by x-ray diffraction, either by powder or single crystal techniques requires a dependable body of reference data. It is not only necessary to have data on each phase which are accurate and complete, it also is desirable to have data on as wide a range of compounds as possible, and to have the data organized in such a manner as to be readily usable. The outstanding compilations which approach these goals are the Powder Diffraction File and Crystal Data.The Powder Diffraction File, published by the Joint Committee on Powder Diffraction Standards has data covering about 22,500 phases, both organic and inorganic. These data are of various degrees of accuracy as is indicated by symbols. The File is continuously being improved by the addition of evaluated data from the general literature and by data produced by supporting projects, the principal one being the Joint Committee Associateship at the National Bureau of Standards.To be noted in the File with a star, and to be truly considered standard data a powder pattern must be complete in the sense of including all reflections above the minimum “d” spacing covered, both weak lines and those with large “d” spacings. Since the best test of a pattern is its own internal consistency, the reflections must all have hkl's assigned and must show a good agreement between the spacings observed and those calculated from a refined cell, and they must be consistent with the known space group. This agreement can be best obtained by the use of an internal standard and a computer program. The intensities should be measured by a method which minimizes the effect of crystal orientation.The PDF is provided with search procedure manuals arranged on a scheme of the strongest lines to help in locating data matching that from an unknovm. A computer program for rapid searching is available. A recent development is the inclusion of a “reference intensity” to aid in estimating the quantitative analysis of mixtures.Crystal Data is a compilation now in the third edition made at the National Bureau of Standards and published by the Joint Committee on Powder Diffraction Standards. It contains data on the unit cell parameters of over 24,000 phases. These data are arranged by crystal system and axial ratios to simplify identification of phases from unit cell data obtained from Single crystal cameras.Both of these large compilations are also important reference sources for crystallographic information giving structural information and literature references.

Author(s):  
Michel Fleck ◽  
Ekkehart Tillmanns ◽  
Ladislav Bohatý ◽  
Peter Held

AbstractThe crystal structures of eight different L-malates have been determined and refined from single-crystal X-ray diffraction data. The compounds are the monoclinic (space groupIn addition, for all the compounds, powder diffraction data were collected, analysed and submitted to the powder diffraction file (PDF).


1987 ◽  
Vol 2 (3) ◽  
pp. 187-190 ◽  
Author(s):  
Kjell R. Waerstad ◽  
A. William Frazier

AbstractX-ray powder diffraction and single-crystal data are reported for a series of isomorphous compounds with the general chemical composition (Fe,Al)3(K,NH4,H3O)H14 (PO4)8·4H2O. The compounds are monoclinic with space group C2/c. Unit-cell parameters were determined on the mixed salt (Fe0.84,Al0.16)3KH14(PO4)8·4H2O, as obtained from sludge precipitated in commercial shipping-grade wet-process phosphoric acid. Single-crystal studies and refined powder diffraction data provided unit-cell parameters of a= 16.908(9) Å, b = 9.588(2) Å, c = 17.539(5) Å, and β = 91.06(4)°.


1993 ◽  
Vol 8 (2) ◽  
pp. 107-108 ◽  
Author(s):  
G. Bandoli ◽  
A. Ongaro ◽  
F. Lotto ◽  
M. Rossi

X-ray powder diffraction of Nitrofurantoin C8H6N4O5 reveals that the compound crystallizes in a monoclinic unit cell with the powder data unit cell parameters of a = 7.852(2), b= 6.497(1), c = 18.927(5) Å, β=93.15(2)°, V=964.1(2) Å3. The unit cell dimensions determined by single crystal agree very well with those of powder diffraction analysis. A comparison with the Powder Diffraction File (PDF) 34-1603 indicates that the present data provide a more precise match to the unit cell, include additional weak reflections, along with the indexing of the powder pattern.


1997 ◽  
Vol 12 (2) ◽  
pp. 81-86 ◽  
Author(s):  
J. M. S. Skakle ◽  
L. P. Moroni ◽  
F. P. Glasser

The X-ray powder diffraction patterns for two new synthetic calcium uranium (VI) silicate hydrate phases are reported. Ca1.5U6(OH)7O16·7H2O is orthorhombic, space group P*a*, with unit cell a=13.8949(14), b=12.0776(12), c=15.228(3) Å. The structure appears to be related to that of becquerelite. Ca2(UO2)2(Si2O5)3·10H2O was also indexed on an orthorhombic unit cell, a=12.075(3), b=15.406(6), c=26.043(6) Å. The Powder Diffraction File coverage of uranium-containing minerals which could, on the basis of their chemical formula, form in U-containing cements is also reviewed.


2000 ◽  
Vol 15 (2) ◽  
pp. 130-133 ◽  
Author(s):  
N. Subramanian ◽  
N. V. Chandra Shekar ◽  
P. Ch. Sahu ◽  
Mohammad Yousuf ◽  
K. Govinda Rajan

This paper presents the powder X-ray diffraction data of BaFI recorded using a Guinier diffractometer and Mo Kα1 radiation. BaFI stabilizes at standard temperature of 25 °C and standard-atmospheric pressure (STP) in the tetragonal structure (space group P4/nmm; No. 129) with lattice parameters a=4.660(1) Å and c=7.960(5) Å. Our observed pattern is different from the existing observed powder diffraction data reported in the PDF files 34-716 (Beck, 1976) and 31-139 (), but matches almost perfectly with the pattern calculated by us from the reported single crystal data ( and with the calculated data available in PDF file 70-0481. Further, our data provide a number of new Bragg peaks extending beyond the range of d values available in the existing PDF files.


2019 ◽  
Vol 17 (1) ◽  
pp. 1116-1123
Author(s):  
Jin-Hui Zhou ◽  
Mao-Jian Shi ◽  
Lin Ding ◽  
Guo-Qiang ShangGuan ◽  
Jun Xu

AbstractThe crystal structures of the title compound, C27H26ClN3O2, were established by single-crystal X-ray diffraction and synchrotron radiation X-ray powder diffraction. The simulated annealing approach and rigid-body Rietveld refinement were applied to the structure solution from powder data. Direct methods and full-matrix least-squares techniques were used to solve and refine the crystal structure from single-crystal data. The title compound crystallized in space group P $\bar{1}$ with lattice parameters a=17.396(7) Å, b= 10.010(4) Å, c=6.833(3) Å, α=77.345(12) °, β= 93.534(6) °, γ=97.210(9) °, unit-cell volume V= 1151.0(2) Å3, Z=2 from powder data, and in space group P $\bar{1}$with lattice parameters α=82.485(2) °, β= 86.5110(10) °, γ=77.518(2) °, a=6.8159(6) Å, b= 10.0003(9) Å, c=17.4140(15) Å, unit-cell volume V =1148.3(2) Å3, Z=2 from single-crystal data. No detectable impurities were observed.


2002 ◽  
Vol 17 (3) ◽  
pp. 244-246
Author(s):  
Ailette Aguila Tobien ◽  
Peter Varlashkin

The current JCPDS powder pattern for the racemic compound fenoprofen calcium dihydrate (card No. 44-1790) is unindexed. Previously we reported the single crystal data, determined at −100 °C, for this material (Zhu et al., 2001). Using 2θ values obtained from a powder pattern spiked with internal standards, we indexed the room temperature powder pattern. The resulting unit cell values for the monoclinic P21/n cell are a=19.018 Å, b=7.738 Å, c=19.472 Å, β=91.66°.


1982 ◽  
Vol 26 ◽  
pp. 87-88 ◽  
Author(s):  
Winnie Wong-Ng ◽  
Mark Holomany ◽  
W. Frank McClune ◽  
Camden R. Hubbard

The Powder Diffraction File (PDF), published by the JCPDS-International Centre for Diffraction Data, is one of the most widely used scientific data bases. It currently consists of about 40,000 x-ray diffraction patterns, organized into 32 sets and 5 subfiles: metals and alloys, minerals, common phases, forensic patterns, and those from the National Bureau of Standards (NBS), New patterns are being added to the PDF at a rate of 2,000 patterns per year. The sources of these patterns are the literature, private contributions, grants in-aid projects, and the JCPDS Associateship at the NBS.


2021 ◽  
pp. 1-2
Author(s):  
James A. Kaduk ◽  
Amy M. Gindhart ◽  
Thomas N. Blanton

Commercial escitalopram oxalate crystallizes as a hydrated adduct with oxalic acid, in the space group P21 with a = 8.029897(21), b = 25.09397(6), c = 11.138930(31) Å, β = 106.7759(2)°, V = 2148.992(7) Å3, and Z = 4. The agreement of the Rietveld and previous single-crystal structures is excellent; the root-mean-square Cartesian displacements of the non-H atoms of the two independent cations are 0.076 and 0.067 Å, respectively. The water molecule refined to a slightly different position and occupancy. The pattern is included in the Powder Diffraction File™ (PDF®) as entry 00-064-1507.


1996 ◽  
Vol 11 (4) ◽  
pp. 301-304
Author(s):  
Héctor Novoa de Armas ◽  
Rolando González Hernández ◽  
José Antonio Henao Martínez ◽  
Ramón Poméz Hernández

p-nitrophenol, C6H5NO3, and disophenol, C6H3I2NO3, have been investigated by means of X-ray powder diffraction. The unit cell dimensions were determined from diffractometer methods, using monochromatic CuKα1 radiation, and evaluated by indexing programs. The monoclinic cell found for p-nitrophenol was a=6.159(2) Å, b=8.890(2) Å, c=11.770(2) Å, β=103.04(2)°, Z=4, space group P21 or P2l/m, Dx=1.469 Mg/m3. The monoclinic cell found for disophenol has the dimensions a=8.886(1) Å, b=14.088(2) Å, c=8.521(1) Å, β=91.11(1)°, Z=4, space group P2, P2, Pm or P2/m, Dx=2.438 Mg/m3.


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