dubfan
Critical Thinker
- Joined
- May 4, 2006
- Messages
- 452
As predicted, the next battleground is shaping up to be sulfidation of the WTC steel. Sadly, I don't have the chemistry chops to take this one up even though Greening has a convincing bit of stoichiometry and the "Scholars" have....who knows. Unfounded assertions & confirmation bias, it appears.
If you're just joining us a brief recap. One of the enduring mysteries of 9/11 has been the presence of sulfur contaminants observed on some of the WTC steel. The source and mechanism of this contamination has never been conclusively identified. The CTs -- of course -- immediately leapt to the conclusion that it's evidence of "thermate" (thermite enriched with sulfur to enhance its cutting effectiveness).
It turns out that the gypsum sheetrock in the WTC (which was obviously used in massive quantities) is pure hydrous calcium disulfate. So the basic issue at present is in either confirming or ruling out the sheetrock as a source of the elemental sulfur that caused the contamination.
The relevant Looser post is here:
http://s15.invisionfree.com/Loose_Change_Forum/index.php?showtopic=6763&view=findpost&p=5544918
Excerpt:
If I'm not mistaken, it's not elemental sulfur that's required, it's sulfuric acid. Furthermore, the first point -- about the water being driven off -- seems suspect to me (given Greening's analysis, below) because it ignores the catalytic effect of carbon monoxide on the reaction.
The Greening paper is here:
http://911myths.com/Sulfur.pdf
Excerpt (pp. 3-4):
So, if I'm following Greening, he's saying, yeah, BUT, we had a fuel-rich fire going there, and therefore a lot of CO, so it's possible some elemental sulfur was liberated from the sheetrock and that's where we got all this sulfur contamination.
Any chemists in the house?
ETA: page number refs to the Greening paper, spelling ("difulfate", geez)
If you're just joining us a brief recap. One of the enduring mysteries of 9/11 has been the presence of sulfur contaminants observed on some of the WTC steel. The source and mechanism of this contamination has never been conclusively identified. The CTs -- of course -- immediately leapt to the conclusion that it's evidence of "thermate" (thermite enriched with sulfur to enhance its cutting effectiveness).
It turns out that the gypsum sheetrock in the WTC (which was obviously used in massive quantities) is pure hydrous calcium disulfate. So the basic issue at present is in either confirming or ruling out the sheetrock as a source of the elemental sulfur that caused the contamination.
The relevant Looser post is here:
http://s15.invisionfree.com/Loose_Change_Forum/index.php?showtopic=6763&view=findpost&p=5544918
Excerpt:
Also remember that the 3rd most used substance in the WTC tower was a sulphur based drywall.
Rulling that out as the source of the sulphur is crucial.
S911T forum:
Nearly all the sulphur present is in sulphate form, calcium sulphate. All that will happen if you heat it in a kero fire is that any water present will be driven off. In fact that is the method used to make drierite, a dehydrating agent, obtained by heating to 650 deg C.
Even materials like rubber will, if burnt, release SO2, not free sulphur. To penetrate steel free sulphur would be required.
If I'm not mistaken, it's not elemental sulfur that's required, it's sulfuric acid. Furthermore, the first point -- about the water being driven off -- seems suspect to me (given Greening's analysis, below) because it ignores the catalytic effect of carbon monoxide on the reaction.
The Greening paper is here:
http://911myths.com/Sulfur.pdf
Excerpt (pp. 3-4):
Chemists have investigated the thermal decomposition of gypsum, CaSO4.2H2O or anhydrite, CaSO4,
since the early 1900s because of its potential for making sulfuric acid by the liberation of SO2 or SO3
from a plentiful and inexpensive starting material /7/. It was known at this time that the direct reaction:
CaSO4 -> CaO + SO3 + 1/2 O2
(followed by: SO3 + H2O -> H2SO4), only proceeds at an acceptable rate at temperatures ~ 1400 degC.
However, early research showed that the above reaction could be accelerated by additives such as clay
and, more importantly, the reduction of CaSO4 to CaO and SO2 by reaction with solid carbon or gaseous
carbon monoxide was found to be possible at temperatures well below 1000 degC /8/. In these cases CaSO4
was decomposed by two novel reactions:
2CaSO4 + C -> 2CaO + CO2 + 2SO2
and,
CaSO4 + CO -> CaO + CO2 + SO2
Since the 1980s there been renewed interest in these reactions because of their role in the removal of SO2
from combustion gases by contact with lime (CaO) in so-called flue gas desufurisation processes, (See,
for example /9/ and references contained therein.). As a consequence, the chemistry of calcium sulfate
reduction has been investigated over a wide range of conditions. Thus, for example, R. Kuusik and co-
workers (See Ref/10/), have reported details of the thermal decomposition of calcium sulfate in carbon
monoxide/nitrogen mixtures and note that in 10 - 20 % CO/ N2, calcium sulfide, CaS, and carbon dioxide
are formed at temperatures in the range 780 - 850 degC, while at CO concentrations below 10 %, calcium
oxide, CaO, carbon dioxide and sulfur dioxide are formed above 900 degC. Kuusik et al. also note that the
presence of impurities such as SiO2 in the calcium sulfate lower the decomposition temperatures by up to
100 degC.
Published data /11/ on the kinetics of the reduction of calcium sulfate indicate that about 0.1 % per minute
conversion to SO2 would occur for CaSO4 maintained at 900 degC in an atmosphere containing 1 % CO. If
we assume that similar temperature and carbon monoxide impurity concentrations prevailed for 30
minutes in the combustion gases from the WTC fires, about 240 kg of SO2 would have been released
within each WTC Tower by decomposition of gypsum wallboard. If we further assume, as was done for
the live load production of SO2, that the decomposition gases accumulated in a volume of 10,000 m3 and
the effective air exchange rate was four floor-volumes per hour, the maximum concentration of SO2 from
the decomposition of gypsum was 12 grams / m3, equivalent to 0.42 vol % SO2.
So, if I'm following Greening, he's saying, yeah, BUT, we had a fuel-rich fire going there, and therefore a lot of CO, so it's possible some elemental sulfur was liberated from the sheetrock and that's where we got all this sulfur contamination.
Any chemists in the house?
ETA: page number refs to the Greening paper, spelling ("difulfate", geez)
Last edited: