[Ifeffit] S XANES question
Matthew Marcus
mamarcus at lbl.gov
Wed Nov 26 16:46:00 CST 2014
Yup, that's what mine looks like, if done with TEY to avoid overabsorption. For calibration, I use FY and take the peak position as
the calibration. Yours also looks tolerably like the apatite spectrum in the cited paper (copied here:
file:///C:/Users/admin/Downloads/02e7e526633b903125000000%20(1).pdf), figure 1. It does not look like their
gypsum spectrum.
mam
On 11/26/2014 2:30 PM, Matt Newville wrote:
> Hi Matthew, Lyle,
>
> I'm still learning S XANES, but when we've measured gypsum, it looks very comparable to the spectra from ID21:
> http://www.esrf.eu/UsersAndScience/Experiments/Imaging/ID21/php/gypsum
>
> We often use the spectra from there as references (or when asking: Is this "standard" what we think it is?)
>
> --Matt
>
>
>
> On Wed, Nov 26, 2014 at 4:23 PM, Matthew Marcus <mamarcus at lbl.gov <mailto:mamarcus at lbl.gov>> wrote:
>
> The gypsum spectrum looks nothing like any spectrum of gypsum or other sulfate I've ever seen. I'm deeply suspicious.
> mam
>
> On 11/26/2014 1:36 PM, Lyle Gordon wrote:
>
> Matthew,
>
> Paris et al in 2001 reported higher S K-edge white line energies for SO4 in Apatite, 2 eV above Gypsum.
>
> THE VALENCE AND SPECIATION OF SULFUR IN GLASSES
> BY X-RAY ABSORPTION SPECTROSCOPY
> The Canadian Mineralogist
> Vol. 39, pp. 331-339 (2001)
>
> -Lyle
>
> On Wed, Nov 26, 2014 at 12:39 PM, Matthew Marcus <mamarcus at lbl.gov <mailto:mamarcus at lbl.gov> <mailto:mamarcus at lbl.gov <mailto:mamarcus at lbl.gov>>> wrote:
>
> A user on ALS 10.3.2 is taking S K-edge XANES and consistently finding a strong peak at 2484eV (calibration: gypsum white line = 2482.75eV).
> There's a shoulder at the nominal position of the sulfate peak. Now, peaks below sulfate I can understand, but since there's no such
> thing as heptavalent sulfur, what could give a peak *above* the sulfate white line? Anybody ever seen that? Yes, we checked calibration.
> mam
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