If the use was originally for the neutron case, how is it applicable to the x-
ray case in general and to the "laboratory x-ray diffractometer" in particular?
If the original intent was to describe the "optics" of a particular instrument,
shouldn't the function be determined for the instrument - using an appropriate
calibration standard - and then fixed? Shouldn't the function be the same for
all samples? Am I missing something?
Comments, please!
Frank May
Monsanto Company
St. Louis, MO U.S.A.
314 694 1580
FLMAY@ccmail.monsanto.com