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. 203

Figure 2.10.9 

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 2.10.9]
Figure 2.10.9

A rocking curve (ϕ scan) of (Ba0.7Sr1.3)TiO4, with the detector fixed at 9.647° 2θ, the top of a strong peak in the synchrotron pattern. The jagged plot is from a static specimen, and shows individual grains moving in and out of diffracting position. The flat curve is from a rotating specimen, and indicates that a powder average was obtained.