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Re: The case of the missing elements


 

Cool.?

Geo

----- Original Message -----
From: Dude <dfemer@...>
To: [email protected]
Sent: Sat, 08 Feb 2020 23:13:48 -0500 (EST)
Subject: Re: [XRF] The case of the missing elements

Geo,

Jaw crusher, 110v motor, weights about 200lbs on a stand. It sits
in the mancave and its easier to bring rocks to it than it to rocks.

Dud

?

?

?

From: [email protected]
[mailto:[email protected]] On Behalf Of GEOelectronics@...
Sent: Saturday, February 8, 2020 9:16 AM
To: [email protected]
Subject: Re: [XRF] The case of the missing elements

?

"I use a Rock crusher for big rock samples" Pics? Manual?
Portable (trailer hitch mount)?

?

Geo

?

-----
Original Message -----

From: Dude <dfemer@...>

To: [email protected]

Sent: Sat, 08 Feb 2020 00:36:20 -0500 (EST)

Subject: Re: [XRF] The case of the missing elements

?



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I use a
Rock crusher for big rock samples.? Most are just

done in using a cloth covered hammer and then a ceramic mortar and pestle then
sieving

the powder down to a uniform and appropriate size.? Yeah, I don¡¯t

crush my nice specimens but I do when I have a bulk prospecting ?sample.

Using a
rock saw to get a flat surface cut to look at the homogeneity

of the rock is useful as well then selecting the target area to shoot

The
biggest issue I see with trying to determine what a mineral is,

is using the elemental composition to justify what Mindat says should be in

it.? If it¡¯s a single crystal that¡¯s ok, but to shoot a whole

rock and make a definitive statement that its¡± leaverite¡± is wrong

as you have no idea what is fluorescing, a xtal? the matrix? or the host rock¡¯s

body - anyone of which will introduce its own elements.?

?Dud

From:
[email protected]

[mailto:[email protected]] On Behalf Of WILLIAM S Dubyk
Sent: Friday, February 7, 2020 9:02 PM
To: [email protected]
Subject: Re: [XRF] The case of the missing elements

?

Powdering

a specimen is a common and practical way of getting a uniform xrf, but like you

mentioned Dud, us collectors do cringe at that especially if it is unusual,

expensive, and/or hard to replace. Microprobe analysis of specimens is maybe a

little worse, where a chunk has to be taken out of the mineral.

?

How

would you prepare a sample like that? Taking a piece off with a Dremel or even

a cheese grater might introduce contamination. Do you know how labs do it, and

can we do this in the home lab? I have some samples I can use so I am willing

to give it a try.

?

Steve

?


From:
[email protected] <[email protected]> on behalf of Dude

<dfemer@...>
Sent: Friday, February 7, 2020 9:37 PM
To: [email protected] <[email protected]>
Subject: Re: [XRF] The case of the missing elements

?

Good points here Geo. However we¡¯re all doing this all wrong

and comparing apples to oranges.?

The excitation sources have widely different energies and source

strength and exposure is from within or on the surface.? Worse yet we have

no idea of the elemental distribution in the matrix which is going to determine

what gets excited and what gets absorbed. ?What is the gamma activity of

the Cerite? What¡¯s the mass. Is this a big boy or a chip?

The excitation energy from the Th is going to be very high while

the Am is lower in energy and has the Np x-rays which are closer and stronger

to excite the absorption edges of both the Fe and Y.? But the biggest

problem is just what are you exciting and where is it ¨C on the surface,

deep inside just a small xtal?

To properly compare these measurements the rock should be
pulverized

down to 200 u or so (Charles just cringed) ?mixed and homogenized and put

into a XRF cup with a mylar cover and then measured.? It makes for a

homogenous mixture removing the ambiguity of what the matrix effects are.

I think Geo is right in the density- thickness problem and the

different source ?strengths.

Charles, I have an external ?higher activity natural

?source that I think you might like to try, give me a call

Dud

?

?

?

From: [email protected]

[mailto:[email protected]] On Behalf Of GEOelectronics@...
Sent: Friday, February 7, 2020 4:55 PM
To: [email protected]
Subject: Re: [XRF] The case of the missing elements

?

Hi

Charles, cool observation. If I may guess at it:

?

We

know from experience that an atom will make XRF if excited by energy from

alpha, beta (or electron stream) Gamma, X-Rays etc. Probably many other ways

too.

?

So

if you rely on internal energy to do this, it will do so in response to the

available radiation from the rock. Some have LOTS, some have very little, some

almost none.

?

One

advantage to that way is all the atoms, even those deep within a big rock are

being excited. If those XRF rays can get out depends only on the energy of the

ray and the overburden.

?

Rays

above 50 keV have little problem penetrating silicon-calcium-oxygen atoms.

This

goes for adding external energy or gathering internally generated XRF.

?

So

your method might show up something that an external exciter misses.

?

But

a good exciter will work on a rock that has no discernable radioactivity, the

thing is how radioactive is the rock and how radioactive is does the external

exciter have to be to equal or better it.....

?

The

pro units have a need for speed so they have X-Ray tubes, blasting the sample

with as much as the law allows. We don't actually have a need for speed so we

can use tiny little exciters, but as far as the elements at the surface and a

little further inside are concerned, it is much more "exciting" than

the stuff coming from deep inside and spread over the entire surface of the

rock.

?

In

other words it may be small, but it is concentrated where it counts, we

substitute long run times to get the results we need.

?

Say

on another note, do you have enough Trinitite to do some Gamma Spec runs on it

with your Si-PIN? You could precisely calibrate the detector with Am, the see

if the X-Rays coming from Trinitite are from Np or U atoms, or both.

?

Geo

?

?

-----

Original Message -----


From: Charles David Young <charlesdavidyoung@...>


To: [email protected], Mike Loughlin <loughlin3@...>


Sent: Fri, 07 Feb 2020 17:12:15 -0500 (EST)


Subject: [XRF] The case of the missing elements

?

I

recently picked up a specimen of melanocerite-Ce at the mineral show and did a

scan without Am241 by depending on the internal radiation.? I was not

surprised to see Th La Ce and Nd in the blue plot.

?

Then

I wanted to see if I got the same results using Am241 as an additional

exciter.? So I carefully moved the specimen just far enough from the

detector to allow me to slide in the Am241 jig.? I was careful to keep the

same spot on the rock even though it looked quite uniform.

?

Curiously

I am now getting additional strong Fe and Y peaks in the red plot.? What

could account for this?? I am not surprised that the La Ce Nd are lit up

as they are.

?

I

have also attached both .mca files in case one wishes to analyze them.?

However, I am not really asking for that.? I would just like to understand

why the Am241 lights up the Fe and Y so strongly compared to the internal

radiation.? It is kind of a pain to weed through the Am241 background

peaks but it appears that I may not get a complete picture with the internal

radiation alone.

?

Charles

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