Hi all, In my defense, 10 of the 12 messages relating to this topic have had their footers attached. I will try to figure out how to get rid of it for next time.
Here is a topic I am interested in: we are collecting a lot of data on an imaging plate (GSECARS and HPCAT at Advanced Photon Source). We are interested in splitting of peaks in some of the samples. The splitting is very difficult to see on the integrated pattern, but very easy to see on the 2-D imaging plate frame itself. The rings are "spotty" and it's very easy to tell which spots are in which ring when the peak is slightly split. My question is whether there is software I can use to take advantage of this and fit the "spots" so I can get a better resolution of the splitting. Something in between powder and single crystal. Thank you, - Kurt -----Original Message----- From: Larry Finger [mailto:larry.fin...@gmail.com] On Behalf Of Larry Finger Sent: Friday, May 08, 2015 9:58 AM To: Kurt Leinenweber; Alan Hewat; Leopoldo Suescun Cc: rietveld_l@ill.fr Subject: Re: regress in crystallographic good practices and knowledge On 05/08/2015 11:16 AM, Kurt Leinenweber wrote: > Hi Alan, > > I still like the Rietveld list and do read all the posts. > > Is it possible to block attachments so that people can’t attach files any > more? > > -Kurt Thus writes the guy whose mailer blindly attaches a message footer rather than in-lining a signature. :) Although I no longer practice crystallography, and no longer read the literature, I do find the discussions here of interest. At least I can follow how little crystallography the average solid-state researcher actually knows. Sad to know that bugs in a few programs could completely derail the science. All the greats of the early part of the 20th century must be really spinning in their graves! Larry
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