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XRF Wiki
Welcome to the XRF Wiki. This Wiki is a repository of information contributed by members of [email protected]. Members can view and edit the pages. The pages are currently not viewable by the public. The pages below represent a rough overview of the technology and techniques associated with X-Ray Florescence Spectroscopy as well as serving as a place for members to organize the spectra that they have contributed to the forum.?
As a starting point, the pages will be populated by information taken from member posts from the past few years - with references/attribution. Perhaps in time, these pages can be edited by members to make them more complete and less choppy. Members can also edit this page, making the structure of the content more organized.?
Pages can contain information about a particular topic, links to relevant resources (such as manuals, research papers, etc.), links to relevant forum discussions on the topic, book titles, or anything that might be useful.
What follows is very much a work in progress.
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Adding to the Wiki
For those unfamiliar with the Wiki phenomenon, it is basically a user editable encyclopedia. The idea is that there are pages with different articles, which the user can read and also choose to edit if desired. If a piece of information is incorrect, a link outdated, or the presentation choppy or unclear, the user can just click "Edit Page" at the bottom and then fix the mistake. There is also a "Page History," so if you a user were to make a mistake or maliciously destroy a page (which wouldn't happen here) an editor can come along and restore the page to a previous version.?
If you have used MediaWiki (the engine that runs behind the scene of Wikipedia.org) you will be familiar with a certain style of creating an article. There are tags that one uses to change the formatting of the parts of the article. The Wiki on Groups.io uses a different background engine and so the standard MediaWiki syntax does not apply here. Rather, the page is edited using the same tools as one would use to compose a message on the forums. If you are a programmer or someone who likes using the tagged syntax directly, you can access the underlying page source code, be activating the advanced editing toolbar (the icon with three lines on the far right of the basic toolbar) and then clicking on the source code icon <> on the far right of the Advance Editing Toolbar. You will immediately notice that the underlying source code is HTML. Most things can be done just by using the various icons, but advanced features like table can only be implemented by manually writing the source code. (Although there are website available that will generate the source code for you through a graphical interface.)
Here are some useful resources from Groups.io:?
Wiki Guide for Users and Editors
Message Composition Tips and Tricks
Overview of XRF
X-Ray Florescence vs. X-Ray Diffraction
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Hardware
This section describes the hardware used for XRF. We will describe the basic theory of operation of each stage in the processing tool chain and then present different commercial systems that are available as these systems are often integrated together.
[Editor note: General theory needs to be in an independent page separate from specific manufacturer information.
[Editor note - question: Should this be arranged by category, e.g detectors, preamps, etc or by manufacturer with the manufacturers product line on one page. Perhaps it's best to put a list of products with theory but the details of the products on a manufacture page...]
Detectors?- what's available, theory of operation, tradeoffs
Detector Cooling?- keeping detectors cool to avoid thermal noise and keeping the TEC from overheating
Preamps?- theory of operation, brief summary of what out there (and what not to do - such as trying to use a PMT preamp for a SiPIN diode...)
Pulse Processing Theory - high level overview of the stages of going from detector pulse to channel peaks on the computer
Commercial Systems - many commercial systems are integrated so it seems to make sense to present, for example all Amptek products together. [question: are their other affordable integrated systems besides Amptek?]
Amptek XRF System
Activation Sources - what do you use to make the sample fluoresce (that's within the amateur budget and doesn't require special licensing)
Software
- Device Control Software - what do you use to collect the data from the detector system
- XRF Analysis Software - what do you use to analyze the data, especially for quantitative measurements (composition percentages, thin film measurement)
- Free Software Tools
Note: there may be software packages that possess some or all of these characteristics.
Materials Spectra
Metals Spectra
Historic/Archeological Spectra
Reference Materials Spectra
Household Objects Spectra
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Resources
Videos
Articles
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Non-XRF Techniques
Gamma Spectroscopy
Raman Spectroscopy
FTIR - Fourier Transform Infrared Spectroscopy
Atomic Emission Spectroscopy
Inductively Coupled Atomic Emission Spectroscopy
Spark Emission Spectroscopy
Atomic Absorption Spectroscopy
LIBS - Laser Induced Breakdown Spectroscopy
Photoacoustic Spectroscopy
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Re: Si-PIN Detector Background?
3600s BG scan running on the one in the chamber- using it's current fine tuned peak value of 4.8us.
Over this winter I'll redo all the element scans from my article on APXS/XRF with the Si-PIN detector and CdTe detector. That will be the final chapter until some iridium shows up- what was thought to be Ir in the original NaI(Tl) scans were later confirmed with the SDD to actually be W. Grrrrrrrrr..........That was my SECOND mistake! Geo |
Re: Si-PIN Detector Background?
¿ªÔÆÌåÓýIt would be interesting to see what that same run would look like but using a 4 usec peaking time. Dud ? From: [email protected]
[mailto:[email protected]] On Behalf Of GEOelectronics@...
Sent: Thursday, October 15, 2020 5:08 PM To: [email protected] Subject: [XRF] Si-PIN Detector Background? ? Someone asked about background counts on the Si-PIN
detector. |
Re: Supplements exposed
Yes DPPMCA is for a real technician........You can also download the program, but to use it you must buy the code key. Geo ----- Original Message ----- From: taray singh via groups.io <sukhjez@...> To: [email protected] Sent: Thu, 15 Oct 2020 20:45:34 -0400 (EDT) Subject: Re: [XRF] Supplements exposed Geo I have previously downloaded this Fp software manual. It helps me understand the limitations of Dpmcca Taray |
Si-PIN Detector Background?
Someone asked about background counts on the Si-PIN detector.
That's always the first thing to test with a new one.? This is a 1 hour scan on SN-18812, no source or X-Rays around, minimal if any shielding. Notice the highest count at ~28 keV = 1 CPH - sweet. Probably Cosmic Ray muons. Geo |
Re: Trinitite Sub Topic 1 Where's the Uranium?
Low-Level Determination of Plutonium by Gamma and?L X-ray Spectroscopy
? ? ? ? ? ? ? ? ? ? ? ? ? ? ? ? Heino Nitsche, Raymond C. Gatti, Shan C. Lee
? ? ? ? ? ? ? ? ? ? ? ? ? ? ? ? Lawrence Berkeley Laboratory
? ? ? ? ? ? ? ? ? ? ? ? ? ? ? ? University of California
? ? ? ? ? ? ? ? ? ? ? ? ? ? ? ? Earth Sciences Division
April1991 ?
Accepted for publication in the Journal of?Radioanalytical and Nuclear Chemistry.
This work was supported by the Yucca Mountain Site Characterization Project Office as part of the U.S.?Civilian Radioactive Waste Management Project through the Los Alamos National Laboratory. The Yucca?Mountain Site Characterization Project is managed by the U.S. Department of Energy, Yucca Mountain?Project. This work was performed at the Lawrence Berkeley Laboratory, which is operated by the University?of California for the U.S. Department of Energy under Contract DE-AC03-76SF00098.
ABSTRACT
We have developed an analytical method for detection of 239pu in aqueous samples at?concentrations as low as 10e-10M. This nuclear counting technique utilizes the uranium L X-rays,?which follow the alpha decay of plutonium. Because L X-rays are specific for the element and not for?the individual isotope, the isotopic composition of the plutonium sample must be known. The?counting efficiency in the 11-23 keV range is determined from a plutonium standard, and the?concentration of the sample is then calculated from the L X-ray count and the isotopic composition.
The total L X-ray count is corrected for possible contributions from? other radionuclides present as?impurities by measuring the low-energy gamma spectrum for each contaminant to establish specific?photon/X-ray ratios. The ratios are important when 241Pu and 242pu are measured, because the?respective decay chain members produce non-U L X-rays. This new method can replace the use of
labor-intensive radiochemical separation techniques and elaborate activation methods for analysis of?239pu in aqueous samples. It is also applicable for assaying plutonium in liquid wastes that pose?possible hazards to the environment.
Bingo. Geo |
Re: Supplements exposed
"do see some small peaks on extreme left with my 1024 settings. 1.85 is probably silicon escape peak." Si escape peak is below every major photopeak -1.74keV below. Fortunately it is small compared to photopeak of element. FP software takes that out and adds it back to photopeak. FP is what's in XRF guns etc. Cost is thousands USD. That's how they can do Mg and Al, Si etc. Otherwise uses same hardware as us. Geo ----- Original Message ----- From: taray singh via groups.io <sukhjez@...> To: [email protected] Sent: Thu, 15 Oct 2020 11:28:27 -0400 (EDT) Subject: Re: [XRF] Supplements exposed I do see some small peaks on extreme left with my 1024 settings. 1.85 is probably silicon escape peak. Argon not??emphasized yet I will check out with ur??methods above. Titanium too maybe in white paint. There are other things I am still learning? Slow learner I guess? Hey why don¡¯t you scan ur?? ?iron supplements to see what comes out through the container? Taray On Thursday, October 15, 2020, 11:18 PM, GEOelectronics@... wrote:
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Re: Supplements exposed
" Hey why don¡¯t you scan ur?? ?iron supplements to see what comes out through the container? Taray" It's on the to-do list. Right now researching documents RE: U L-X-Rays. You are fast learner, how long have you had hands on? 10 days? 2 weeks max? wow. Geo ----- Original Message ----- From: taray singh via groups.io <sukhjez@...> To: [email protected] Sent: Thu, 15 Oct 2020 11:28:27 -0400 (EDT) Subject: Re: [XRF] Supplements exposed I do see some small peaks on extreme left with my 1024 settings. 1.85 is probably silicon escape peak. Argon not??emphasized yet I will check out with ur??methods above. Titanium too maybe in white paint. There are other things I am still learning? Slow learner I guess? Hey why don¡¯t you scan ur?? ?iron supplements to see what comes out through the container? Taray On Thursday, October 15, 2020, 11:18 PM, GEOelectronics@... wrote:
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Re: Supplements exposed
taray singh
I do see some small peaks on extreme left with my 1024 settings. 1.85 is probably silicon escape peak. Argon not??emphasized yet I will check out with ur??methods above. Titanium too maybe in white paint. There are other things I am still learning? Slow learner I guess? Hey why don¡¯t you scan ur?? ?iron supplements to see what comes out through the container? Taray On Thursday, October 15, 2020, 11:18 PM, GEOelectronics@... wrote:
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Re: Supplements exposed
Yes low energy limits on Si-PIN, are you seeing Argon gas in your scans? Comes from air, ionized by alpha particles. Paper filter on exciter helps, also lightweight gas purge, even just a small fan. ? Possible to see Ti not in sample but in your environment too. I traced it down to the material on top of the desk, pigment included Ti oxide.... Test everything Geo ----- Original Message ----- From: taray singh via groups.io <sukhjez@...> To: [email protected] Sent: Thu, 15 Oct 2020 09:36:04 -0400 (EDT) Subject: Re: [XRF] Supplements exposed Geo There are supplements in oxide form. One example is Magnesium oxide? Not well absorbed but due to huge Mg load will overcome this obstacle? Mg??oxide supplements may be friendly to xrf . But Si pin don¡¯t reciprocate? Taray On Thursday, October 15, 2020, 8:51 PM, GEOelectronics@... wrote:
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Re: Supplements exposed
Yes low energy limits on Si-PIN, are you seeing Argon gas in your scans? Comes from air, ionized by alpha particles. Paper filter on exciter helps, also lightweight gas purge, even just a small fan. ? Possible to see Ti not in sample but in your environment too. I traced it down to the material on top of the desk, pigment included Ti oxide.... Test everything Geo ----- Original Message ----- From: taray singh via groups.io <sukhjez@...> To: [email protected] Sent: Thu, 15 Oct 2020 09:36:04 -0400 (EDT) Subject: Re: [XRF] Supplements exposed Geo There are supplements in oxide form. One example is Magnesium oxide? Not well absorbed but due to huge Mg load will overcome this obstacle? Mg??oxide supplements may be friendly to xrf . But Si pin don¡¯t reciprocate? Taray On Thursday, October 15, 2020, 8:51 PM, GEOelectronics@... wrote:
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Re: Supplements exposed
taray singh
Geo There are supplements in oxide form. One example is Magnesium oxide? Not well absorbed but due to huge Mg load will overcome this obstacle? Mg??oxide supplements may be friendly to xrf . But Si pin don¡¯t reciprocate? Taray On Thursday, October 15, 2020, 8:51 PM, GEOelectronics@... wrote:
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Re: Supplements exposed
Thanks for the explanation of the molecules Taray!? This is important and answers some questions about confusing scans of mine on similar items. Test everything. Geo ----- Original Message ----- From: taray singh via groups.io <sukhjez@...> To: [email protected] Sent: Thu, 15 Oct 2020 07:59:07 -0400 (EDT) Subject: [XRF] Supplements exposed Hi guys Drug companies label their supplements by molecular weight of the compound. ? So the actual amount of? study element will vary from one compound to another . ? For example 100 mg of Zn oxide will contain more Zn? than 100 mg of Zn citrate. ? Most drugs are weak acids or bases to aid in gut absorption.In this case this is Zn citrate...a weak acid ? But this will increase their molecular weight with less? study element for the same weight of drug ? This may be good for the drug but bad for xrf. ? Drug? companies? produce supplements which are safe ,stable and bioavailable. ? Xrf is never in the picture. ? Furthermore? most of these oral supplements consist of? a chemical matrix of low Z? ingredients in the capsule and? the powder within. ? Altogether? this high molecular weight drugs within a loose matrix will dilute the elements for xrf ? Despite? this , I can? still can do a qualitative xrf check for the mineral element by just scanning though the plastic bottle? with si pin. ? No need for an elaborate lab analysis . ? But the downside is I am not able to detect? ? ? supplements containing lower Z such as boron,calcium or magnesium. ? Here is a scan for Lifeextension Zinc capsules? ? Taray |
Supplements exposed
taray singh
Hi guys
Drug companies label their supplements by molecular weight of the compound. ?
So the actual amount of? study element will vary from one compound to another .
?
For example 100 mg of Zn oxide will contain more Zn? than 100 mg of Zn citrate.
?
Most drugs are weak acids or bases to aid in gut absorption.In this case this is Zn citrate...a weak acid
?
But this will increase their molecular weight with less? study element for the same weight of drug
?
This may be good for the drug but bad for xrf.
?
Drug? companies? produce supplements which are safe ,stable and bioavailable.
?
Xrf is never in the picture.
?
Furthermore? most of these oral supplements consist of? a chemical matrix of low Z? ingredients in the capsule and? the powder within.
?
Altogether? this high molecular weight drugs within a loose matrix will dilute the elements for xrf
?
Despite? this , I can? still can do a qualitative xrf check for the mineral element by just scanning though the plastic bottle? with si pin.
?
No need for an elaborate lab analysis .
?
But the downside is I am not able to detect? ?
?
supplements containing lower Z such as boron,calcium or magnesium.
?
Here is a scan for Lifeextension Zinc capsules?
?
Taray |
Re: XRF of Industrial alloy sheet metal 70 Cu 30 Ni
All good advice Dud. And I agree, but in Feb 2014 I didn't know that yet. Thanks for helping us all get from there to here, and there's so far yet to go. Geo From: "DFEMER" <dfemer@...> To: [email protected] Sent: Wednesday, October 14, 2020 3:39:50 PM Subject: Re: [XRF] XRF of Industrial alloy sheet metal 70 Cu 30 Ni Geo, What beam current where you using? Based on the dead time (DT) of 25% the current could probably be backed off a bit. Note that most of this DT is dealing with the higher energy counts that you¡¯re not interested in due to the 50 kV tube voltage. The optimal approach would be to set the tube HV to just above the energy range of interest. In this case Cu, which has a binding energy of 8.8 keV. So a 10 or 15 kV HV would eliminate all the high energy counting and just optimize the energy range of interest. You would then set a current to keep the dead time in the 10 ¨C 15% range and you could play with the peaking time to optimize the resolution. For low count rates use a long peaking time which will get better resolution and use a shorter time for higher count rates but with lower resolution. When I run an unknown it¡¯ll be 50kV, then a run at 40, then a run at 20 which gets the HV near a general binding energy range which gives a much better resolution and count time and lowers the limit of detection. Dud ? From: [email protected]
[mailto:[email protected]] On Behalf Of GEOelectronics@... ? This is a sample cut from a piece of sheet metal, the assay
printed on it was Cu-70% Ni-30%. |
Re: XRF of Industrial alloy sheet metal 70 Cu 30 Ni
¿ªÔÆÌåÓýGeo, What beam current where you using? Based on the dead time (DT) of 25% the current could probably be backed off a bit. Note that most of this DT is dealing with the higher energy counts that you¡¯re not interested in due to the 50 kV tube voltage. The optimal approach would be to set the tube HV to just above the energy range of interest. In this case Cu, which has a binding energy of 8.8 keV. So a 10 or 15 kV HV would eliminate all the high energy counting and just optimize the energy range of interest. You would then set a current to keep the dead time in the 10 ¨C 15% range and you could play with the peaking time to optimize the resolution. For low count rates use a long peaking time which will get better resolution and use a shorter time for higher count rates but with lower resolution. When I run an unknown it¡¯ll be 50kV, then a run at 40, then a run at 20 which gets the HV near a general binding energy range which gives a much better resolution and count time and lowers the limit of detection. Dud ? From: [email protected]
[mailto:[email protected]] On Behalf Of GEOelectronics@...
Sent: Wednesday, October 14, 2020 12:21 PM To: [email protected] Subject: [XRF] XRF of Industrial alloy sheet metal 70 Cu 30 Ni ? This is a sample cut from a piece of sheet metal, the assay
printed on it was Cu-70% Ni-30%. |
XRF of Industrial alloy sheet metal 70 Cu 30 Ni
This is a sample cut from a piece of sheet metal, the assay printed on it was Cu-70% Ni-30%.
,mca and pics of the scan attached. Later will post pics of setup. Like the pictures indicate - SDD sensor, XRF via W tube, 50kVp @ 10 uA. Cu-Ni-70-30-.005.mca
Cu-Ni-70-30-.005.mca
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AMPTEK_SDD-X-Ray-XRF-50kVp-10uA-Metals_XRF-Cu-Ni-70-30-005-Close-Both.png
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A Penny for your. thoughts or US Cent XRF Fail
XRF of a modern US cent, thin copper over zinc core. One side has the copper removed. XRF of both sides .mca's attached. Exciter = W target tube, @ 50kV / 10 uA
This is a fail because the HV is set to high, and so is the current, causing excitation deeper than need be, allowing Zn to overwhelm the copper signal. Am excitation would prove to be a better choice, in that the Alpha Particles help with surface excitation only. A little common sense prevails. Geo ![]()
US-Cent-XRF.png
Zn-US-2012-Penny-Copper-Side.mca
Zn-US-2012-Penny-Copper-Side.mca
Zn-US-2012-Penny-Copper-Removed-Side.mca
Zn-US-2012-Penny-Copper-Removed-Side.mca
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