Tables for
Volume H
Powder diffraction
Edited by C. J. Gilmore, J. A. Kaduk and H. Schenk
International Tables for Crystallography (2018). Vol. H, ch. 2.10, p. 201

Figure 2.10.2 

P. S. Whitfield,a* A. Huqb and J. A. Kadukc,d,e

aEnergy, Mining and Environment Portfolio, National Research Council Canada, 1200 Montreal Road, Ottawa ON K1A 0R6, Canada,bChemical and Engineering Materials Division, Spallation Neutron Source, P.O. Box 2008, MS 6475, Oak Ridge, TN 37831, USA,cDepartment of Chemistry, Illinois Institute of Technology, 3101 South Dearborn Street, Chicago, IL 60616, USA,dDepartment of Physics, North Central College, 131 South Loomis Street, Naperville, IL 60540, USA, and ePoly Crystallography Inc., 423 East Chicago Avenue, Naperville, IL 60540, USA
Correspondence e-mail:

[Figure 2.10.2]
Figure 2.10.2

2D images of the spotty Debye rings of a coarse (~35 µm) cement powder using a Co Kα radiation 1 mm point source. Overlaid are SEMs of the sample material and integrated patterns from the thin slices indicated in the 2D patterns to illustrate what a point or 1D detector would see. Note: in these 2D data sets the low 2θ rings are on the right-hand side.