I realize that this debate of the Bentham paper is off-topic, but since this thread is past its last hope of usefulness, we might as well say something substantive...
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If we look at the following slide (which is sourced from truther video) then it's quite clear that 70+ % by weight of the material is carbon.
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This is from Marc Basile's presentation and, iirc, studies, which he didn't publish in any proper way, afaik.
I'd be careful with that. We know that there are at least 2 different kinds of red-gray particles in the dust samples, and we know there were at least 2 different kinds of steel primer in the towers. There could easily be more of either. Can we be certain that Basile picked the right kind of flake?
A carbon content of 70%+ is a problem, as are K and Ca contents of 0.4%+ (more than Cr), if that chip is the same material as chips a-d from Bentham.
LaClede primer contains 71.5% organic matrix - so the carbon content should be significantly lower than that. I calculated slightly less than 50% C total in the paint, with the balance being mostly O, H and N (amine epoxy should contain N...).
Also, the most likely source of traces of K and Ca would be impure kaolinite; but aluminiumsilicate is only 11.7% by weight of the primer; with Ca making up about 0.9% of Basile's sample, that would mean that the kaolinite is contaminated with nearly 8% Ca - sounds too much to me.
Conclusion: I think Basile didn't look at the same material as chips a-d; or he worked sloppily; or our LaClede hypothesis is in trouble.
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The sample you discuss here, is it allegedly post-ignition, pre-ignition or a mix?
Ah! Ok... interesting question, I don't know the answer.
But would be very surprised if it isn't pre-ignition, with 70%+ C still in place.
I presume that the "freshly broken" comment implies that the surface is unoxidized or minimally oxidized.
Yes, that, but more importantly the fresh surface is not or only minimally contaminated.
If I can (unlikely) reconstruct my Chemistry 101 on the fly...
Comparing the mass ratios of iron/aluminum & iron/oxygen, even if all the iron were from thermite, only about 70% of the Al and about 10% of the oxygen could be.
This would put an upper bound on the mass % of the sample that could be thermite at about 5%.
[Would you check this. Been a long time since I've done any chemistry, and the ratio sounds way too low to me.]
But if correct, this would apply a 20x multiplier on the energy / unit mass to their results.
[again, this one sounds way high.]
I'd be curious what you got for the same calculation.
Let's see...
Ideal thermite is, by atom count
2 Fe
2 Al
3 O
Atomic weights are
Fe: 55,85 g/mol
Al: 26,98 g/mol
O: 16 g/mol
Inserting that into the atom count, we get the following mass ratios
Fe: 111,69g
Al: 53,96g
O: 48g
Normalizing to 1 unit of Fe, that's
1 part Fe
0.48 parts Al
0.43 parts O
In Basile's graph, we have by weight
Sample 1:
Fe: 2.63%
Al: 1.68%
O: plenty
and
Sample 2:
Fe: 1,73%
Al: 1,29&
Which translates to Fe:Al ratios of 1:0.64 and 1:0.76, respectively.
This means we are short on Fe - Fe is the bottleneck that provides us with an upper bound of possible ideal thermite in the mix. Since Fe is 52.3% by weight in ideal thermite, and 2.63% and 1.73% in Basile's two samples, we get maxima of
Sample 1: 5.01% thermite
Sample 2: 3.31% thermite
Tom, you were spot on with your calculation. Indeed, from this we'd expect to get an energy density in the DSC of at most 0,195kJ/g (3.9kJ/g * 5%) from a thermitic reaction, and the balance from organic combustion, thermal degradation of the organic matrix, and possibly other reactions, all of which are totally unevaluated by Harrit, Jones, Farrer, Basile and the bunch.
PS. I remember that you & Oystein (I believe) mentioned a second test (in addition to Xray diffraction) that would be definitive for thermite. I went looking for it, but couldn't find it. Could you remind me, please.
Uhm don't know what you are talking about
