Gage's next debate

More sulfidized steel questions to prepare for debate epilogue

A recent post from Sunstealer created these questions for me. As you can see, I am slow to learn chemical matters, and hope you'll bear with me as I re-ask some of these questions:

Thermite melts other metals due to the high heat of reaction not by solid state diffusion of a gas into the parent metal which was observed due to sulphides being found below the solid un-melted surface of the steel. Thermite can't do that. UNDERSTOOD.

Secondly no aluminium in the photomicrograph means no thermite. DO YOU MEAN NO ALUMINUM OR NO ALUMINUM OXIDE? ALSO, NO ALUMINUM AT ALL OR NO ALUMINUM IN THE RED-GRAY MICROCHIPS OF PAINT/"THERMITES?"

You can't conclude anything else but high temperature corrosion via sulphidation, oxidation, decarburisation leading to a liquid Fe-O-S causing inter-granular attack. UNDERSTOOD. WOULD KEVIN RYAN AGREE WITH THE PRESENCE OF Fe-O-S AND JUST ASSERT IT CAME INTO BEING VIA THERMATE? ALSO IS IT TRUE THAT 4500 DEGREE THERMATE TEMPERATURES WOULD BREAK DOWN THE Fe-O-S CHEMICAL STRUCTURE ENTIRELY, AS I THINK SOMEONE ELSE ON THIS THREAD ASSERTED?

Where is the aluminium in the corroded steel in the paper you quote? Where is the Sulphur in the Harrit et al paper? It's not there - therefore no thermite/thermate. SOMEHOW I THOUGH HARRIT ET ALL DID FIND SULPHUR SOMEWHERE IN THE DUST; AGAIN DO YOU MEAN IN THE RED/GRAY CHIPS NONE WAS FOUND?

OTHER QUESTIONS: Ryan Mackey asserted in his white paper that we don't really know how the sulfidized steel was created in the first place. Do you agree? My halting research has come up with what looks like speculation (Battery acid from cars, gypsum) but not a solid explanation. Also, is there an estimate out there of what percentage of the steel beams were corroded away in this process? I asserted in the March 6 debate that it was a very small amount, certainly not enough to explain a global collapse of a skyscraper in any event.

Sorry for so many questions. I'm sure you've covered all of these before.
 
The point is: Thermate is the only known explanation for the melted beam. Sulfur from drywall is speculation.

OK - so planting tons of thermate by evildoers without being detected in three of the largest buildings in NYC (2 of the largest in the world) is an accepted explanation, but the fact that these buildings had drywall is speculation?
 
Because it's not like there's much nitrogen in the atmosphere normally? Nice work, Chris; it's good to see you back in contention for the Stundies.

Dave
Oh you've gone and spoilt it now!

What he doesn't understand is that in order to study the effect of CO2 you have to know what the concentration (partial pressure) of CO2 is in the atmosphere that you are studying. So if you just connect a CO2 bottle to the furnace and pump CO2 in then you'll still have oxygen present which will affect the study. So what you do is use CO2 plus an inert gas. That way you can control the partial pressure of the CO2 due to the CO2/N2 ratio. That allows you to study multiple partial pressures which is the reason for the whole exercise. N2 is cheap.

He wouldn't have known that and would have posted some silly nonsense. Then I'd have asked him what the composition of the air he was breathing was. He'd have gone to wiki to find out 79% is Nitrogen. Which debunks himself. Funny.
 
A recent post from Sunstealer created these questions for me. As you can see, I am slow to learn chemical matters, and hope you'll bear with me as I re-ask some of these questions:
It appears that you did not read my post.

Thermite melts other metals due to the high heat of reaction not by solid state diffusion of a gas into the parent metal which was observed due to sulphides being found below the solid un-melted surface of the steel. Thermite can't do that.
Show the scientific source for this claim or stop making it.

That claim is pure denial based on double talk. Sulfur is added to thermite to lower the melting point of the steel. Sample #1 was melted/corroded in a manner consistent with thermate. Describing the process in technical terms and then claiming that proves it wasn't thermite is erroneous.

Secondly no aluminium in the photomicrograph means no thermite.
False. The aluminum is vaporized and escapes as white smoke in the thermetic reaction.
The red/gray chips contain iron oxide, aluminum, and silicate. "It is inconclusive from these data whether the O is associated with Si or Al or both". Thermite paper pg 6.

You can't conclude anything else but high temperature corrosion via sulphidation, oxidation, decarburisation leading to a liquid Fe-O-S causing inter-granular attack. UNDERSTOOD. WOULD KEVIN RYAN AGREE WITH THE PRESENCE OF Fe-O-S AND JUST ASSERT IT CAME INTO BEING VIA THERMATE? ALSO IS IT TRUE THAT 4500 DEGREE THERMATE TEMPERATURES WOULD BREAK DOWN THE Fe-O-S CHEMICAL STRUCTURE ENTIRELY, AS I THINK SOMEONE ELSE ON THIS THREAD ASSERTED?
Much has been "asserted" but nothing has been backed up with reliable scientific sources.

Where is the Sulphur in the Harrit et al paper? It's not there - therefore no thermite/thermate. SOMEHOW I THOUGH HARRIT ET ALL DID FIND SULPHUR SOMEWHERE IN THE DUST; AGAIN DO YOU MEAN IN THE RED/GRAY CHIPS NONE WAS FOUND?
The beam from WTC 7 was melted/corroded in a manner consistent with thermate. It was the sulfur that lowered the melting point.

[FONT=&quot]The nano-thermite found in the dust did not have a significant amount of sulfur. An intelligent person would immediately recognize that these two are not related.

There is evidence that both were present. It takes some very twisted logic to conclude that this evidence proves neither was present.


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He'd have gone to wiki to find out 79% is Nitrogen. Which debunks himself. Funny.
:blush:

Ya got me. I had forgotten that earth's atmosphere is primarily nitrogen.

However

The abstract of the source posted as proof that the sulfur might have come from drywall only confirms that calcium sulfate, not iron sulfate, was produced. Calcium sulfate is not corrosive. It is used as a coagulant in tofu. It then takes another step to separate the sulfur from the calcium before it becomes corrosive.

The "sulfur came from the drywall" is supposition, not science.
 
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The sulfur paper by Greening assumes that the very specific conditions discussed in the Kuusik paper occurred in the Trade Towers and WTC 7. If this were the case then most of the beams and girders would have been effected.

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It's funny how there were just a few corroded beams and no corroded columns. Almost like it was completely a local effect.
 
Sulfur is added to thermite to lower the melting point of the steel.
C7 I need some help to understand how sulphur in thermate lowers the melting point of steel please.

Thermate is one material, steel is the other. What is the mechanism that makes sulphur in one material lower the melting point in another? How doe it work? Thanks.
 
It appears that you did not read my post.

Show the scientific source for this claim or stop making it.

Sure - 8.7 INTERNAL SULFIDATION.


http://www.scielo.br/pdf/mr/v5n3/v5n3a20.pdf - How can parabolic and linear rate constants be calculated if diffusion isn't the determining mechanism as modelled by solutions to f-i-c-k's laws of diffusion? (damn swear filter - picking up this one). Why do we use steels with high nickel and chromium content at high temperatures where sulphur is present in the atmosphere? You are (indirectly) suggesting that we are wrong to do that. You could save the petrochemical and power production industries billions. Why would we use expensive alloys when cheap plain carbon steels will do. Why are people doing things like this? http://www.hbscc.nl/pdf/41 Coal Gasification Pette.pdf


Kinetics, morphology-structure inter-relationship involving iron sulphide films.


Sulfidation of an Fe-23.4Cr-18.6Al (at.%) alloy was investigated in H2S-H2 atmospheres, Pa, at 973 K. It was found over this pressure range that sulfidation after an early transient period followed the parabolic rate law, being diffusion controlled.
http://www.springerlink.com/content/u781144615mq2867/

That claim is pure denial based on double talk.
Just because you don't understand it, doesn't mean it's not true. Instead of throwing a hissy fit, try picking up a text book and learning something.

You should really have learnt by now that I don't make crap up. I can always back up what I say in this regard because I did a degree in metallurgy and all this stuff was covered - If I make stuff up it's easily found out. In my final year, my thesis was on "high temperature corrosion of engineering ceramics". So I had to understand diffusion in order to do the experiments and calculations on the returned data.

Try learning about diffusion before you comment. This is a good paper. http://www.uio.no/studier/emner/mat...ervisningsmateriale/KJM5120-Ch5-Diffusion.pdf
 
False. The aluminum is vaporized and escapes as white smoke in the thermetic reaction.
The last thing you want to be producing in a thermite reaction is gas because the gas will take heat away from the reaction products.

Secondly the boiling point of Al2O3 is 2977 °C. That's at the extreme upper end of temperature that thermite is capable of producing. Infact it's above the reference cited below. Why on earth would you want to take heat out of the reactant products by changing one of them to a gas? Madness!

THERMITE MIXTURES

Thermites are mixtures that produce a high heat concentration, usually in the form of molten products. Thermite compositions contain a metal oxide as the oxidizer and a metal -- usually aluminum - as the fuel, although other active metals may be used.

A minimum amount of gas is produced, enabling the heat of reaction to concentrate in the solid and liquid products. High reaction temperatures can be achieved in the absence of volatile materials; typically, values of 2000-2800°C are reached [3]. A metal product such as iron, with a wide liquid range (melting point 1535°C, boiling point 2800°C) produces the best thermite behavior. Upon ignition, a thermite mixture will form aluminum
oxide and the metal corresponding to the starting metal oxide:

Fe 20 3 + 2 Al -} A1 20 3 + 2 Fe

Thermite mixtures have found application as incendiary compositions and spot-welding mixtures. They are also used for the intentional demolition of machinery and for the destruction of documents. Thermites are usually produced without a binder (or with a minimum of binder), because the gaseous products resulting from the combustion of the organic binder will carry away heat and cool the reaction. Iron oxide (Fe 2O 3 or Fe3O 4 ) with aluminum metal is the classic thermite mixture. The particle size of the aluminum should be somewhat coarse to prevent the reaction from being too rapid. Thermites tend to be quite safe to manufacture, and they are rather insensitive to most ignition stimuli. In fact, the major problem with most thermites is getting them to ignite, and a strong first fire is usually needed.
http://www.waterstones.com/watersto...is+mocella/chemistry+of+pyrotechnics/6747788/

Everytime you post you get debunked. Why do you continue to post nonsense? From now on please cite your sources - I expect them to be scientific ones.

How can anyone take your arguments seriously when almost everything you post on this subject is proven not to be true? It's laughable that you continue. I assume you consider this latest routing (amongst dozens) a mere flesh wound. (Monty Python reference)

Did people also note the remark about the binder? Yep, causes Harrit et al a few problems.
 
...
Show the scientific source for this claim or stop making it.

That's a good, JREFy reply! Let's see if I can do it, too! :)

Sulfur is added to thermite to lower the melting point of the steel.

Show the scientific source for this claim or stop making it.

Sample #1 was melted/corroded in a manner consistent with thermate.

Show the scientific source for this claim or stop making it.

The aluminum is vaporized and escapes as white smoke in the thermetic reaction.

Show the scientific source for this claim or stop making it.

The beam from WTC 7 was melted/corroded in a manner consistent with thermate.

Show the scientific source for this claim or stop making it.

There is evidence that both (nanothermite and thermAte) were present.

Show the scientific source for this claim or stop making it.


...
Much has been "asserted" but nothing has been backed up with reliable scientific sources.

I couldn't agree more with you, Christopher! :cool:
 
Sunstealer

The kind of corrosion that you are talking about takes place over a period of years. The beam from WTC 7 was melted/corroded in weeks at most and possibly in minutes.

Sulfur is a solid that is used in thermate to lower the melting point of steel but sulfur dioxide is a gas. There is no science to support sulfur dioxide being responsible for the melted/corroded beam.

This whole "sulfur from drywall" fallacy is straw grasping. Drywall would not be used as fireproofing if there was any danger of the sulfur being released in any fire.

* * * * *

I don't know the specific process but I have heard that the white smoke is the aluminum. You don't have an EDX of a piece of steel that has been melted by thermate so don't make any claims about how big the aluminum spike should be.
 
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Christopher you sure do have a double standard when it comes to showing evidence for an assertion, don't you?
 
Sunstealer

The kind of corrosion that you are talking about takes place over a period of years. The beam from WTC 7 was melted/corroded in weeks at most and possibly in minutes.

Sulfur is a solid that is used in thermate to lower the melting point of steel but sulfur dioxide is a gas. There is no science to support sulfur dioxide being responsible for the melted/corroded beam.

This whole "sulfur from drywall" fallacy is straw grasping. Drywall would not be used as fireproofing if there was any danger of the sulfur being released in any fire.

* * * * *

I don't know the specific process but I have heard that the white smoke is the aluminum. You don't have an EDS of a piece of steel that has been melted by thermate so don't make any claims about how big the aluminum spike should be.

Rather sums up your problem.
 
Sunstealer

The kind of corrosion that you are talking about takes place over a period of years. The beam from WTC 7 was melted/corroded in weeks at most and possibly in minutes.

The minutes part is a stretch and you know it. You do remember there is a specific temperature that makes all the difference (it's been mentioned before)?
 
Sunstealer

The kind of corrosion that you are talking about takes place over a period of years. The beam from WTC 7 was melted/corroded in weeks at most
I will sort of agree with you on this. We would not normally expect this degree of corrosion by the mechanism of oxidation and sulphidation in such a short space of time. However, when the specimen from WTC 7 (the one from WTC 1 or 2 is slightly different due to copper) is examined we actually find evidence of internal oxidation and sulphidation which is governed by diffusion.

Fig 12 from "Examination of Heavily Eroded Structural Steel from World Trade Center Buildings 1, 2 and 7" shows this

picture.php


Now I've added some pointers to try to make it clearer.

Yellow line - surface - boundary between formally liquid slag/oxide and solid steel. (roughly)

Green arrows - direction of sulphur and oxygen atoms diffusing into steel.

Red arrows - formation of sulphides along grain boundaries in the solid below the surface.

Blue arrow - liquid eutectic penetrating grain boundaries.

Dark Blue line - below this is area of heavy oxidation & sulphidation. Lots of dark and lighter phases present.

So it's there - we can't ignore it. We also can't rule out other factors such as low pH if the Fe-O-S is acting as a sulphate.

and possibly in minutes.
Minutes is out because we simply wouldn't observe the level of sulphides below the solid steel surface along grain boundaries. Takes too long.

Sulfur is a solid that is used in thermate to lower the melting point of steel
Please cite your source for this. I'd like to know how a solid material affects the melting point of a completely different solid material. What's the interaction between the two?

but sulfur dioxide is a gas. There is no science to support sulfur dioxide being responsible for the melted/corroded beam.
And that's the difference. (See paper above). If it's a gas then components of that gas can diffuse into a solid if the temperature is high enough. There are hundreds of papers dealing with SO2 and it's affect on steels because we burn materials that release SO2 - petrochemical and power companies are affected by this.

Carburisation of steels is a classic example of the useful properties of a gas diffusing into a solid - it's used all the time. I've already quoted the paper, but I'll do it again.

http://www.georgevandervoort.com/fa_lit_papers/World_Trade_Center.pdf

I would suggest that if you have issues with that paper then you can contact the authors. One of them; George Vander Voort has a public email address on his site.

This whole "sulfur from drywall" fallacy is straw grasping. Drywall would not be used as fireproofing if there was any danger of the sulfur being released in any fire.
You keep repeating this and we have shown why drywall is used and how it can produce SO2. These reactions have been known about for 100 years or so and are being examined again because the reaction uses CO2. There are also plenty of other sources.
* * * * *

I don't know the specific process but I have heard that the white smoke is the aluminum.
The smoke will be micron sized solid particles of the reactants (and most likely some unreacted reactants[Fe2O3 and Al]) carried in the air along with any water in the thermite mixture (keep the powder dry is an age old phrase).

You don't have an EDX of a piece of steel that has been melted by thermate so don't make any claims about how big the aluminum spike should be.
No I don't. Nor do the truth movement. ;) I would expect the claimant to provide the evidence, but they don't.

I'm not claiming anything about how big the spike should be. I'm simply claiming that a spike should be present. Why would Al disappear? Why would Fe, S and O remain and Al not? The thermite reaction produces Al2O3 from Al so why do we not see it? Why would we not expect it to be present?

We have the EDX from the corroded steel from here http://911research.wtc7.net/wtc/evidence/metallurgy/WTC_apndxC.htm

No Al present.
 
The kind of corrosion that you are talking about takes place over a period of years. The beam from WTC 7 was melted/corroded in weeks at most
I will sort of agree with you on this. We would not normally expect this degree of corrosion by the mechanism of oxidation and sulphidation in such a short space of time. However, when the specimen from WTC 7 (the one from WTC 1 or 2 is slightly different due to copper) is examined we actually find evidence of internal oxidation and sulphidation which is governed by diffusion.
So what? That's what happened but it does not change the fact that the kind of "corrosion" caused by sulfur dioxide takes years.

There has never been a case of melting beams before. The sulfur from drywall is fanciful. It requires a special set of conditions in packed-bed reactor. Greening was just theorizing. He did no testing to see if his theory was valid. That is not science, it is supposition. Do you have any scientific data that those special conditions exist in office fires? Is there any data that sulfur dioxide is released from drywall in office fires? I doubt very much that there is.

Even if sulfur dioxide could be released it would be diffuse. Almost all the sulfur dioxide [gas] would leave with the smoke and what remained would be spread throughout the debris. There is no way any small amount that would be left could somehow concentrate, mix with water and attack in one spot, to the exclusion of all others. This is just plain silly.

C7 said:
and possibly in minutes.
Minutes is out because we simply wouldn't observe the level of sulphides below the solid steel surface along grain boundaries. Takes too long.
By minutes I mean less than an hour. If activated thermate were to drip or pour onto a steel beam the result could be what we see in Sample #1 and the beam Abolhassan Astaneh found
http://img43.imageshack.us/img43/8467/image004fj.jpg
http://img27.imageshack.us/img27/6197/astanehbeam.jpg

C7 said:
Sulfur is a solid that is used in thermate to lower the melting point of steel

Please cite your source for this. I'd like to know how a solid material affects the melting point of a completely different solid material. What's the interaction between the two?
FEMA detailed the reaction. You can read more here:
[FONT=&quot]http://www.911research.wtc7.net/wtc/evidence/metallurgy/index.html

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C7 said:
but sulfur dioxide is a gas. There is no science to support sulfur dioxide being responsible for the melted/corroded beam.
And that's the difference. (See paper above). If it's a gas then components of that gas can diffuse into a solid if the temperature is high enough.
There are hundreds of papers dealing with SO2 and it's affect on steels because we burn materials that release SO2 - petrochemical and power companies are affected by this.
You keep trying to make the same argument using different words but all your bombast and bluster does not change the fact that sulfur dioxide corrosion is a slow process that takes place over a period of years.

There's nothing in that paper that says sulfur dioxide had anything to do the excessive melting/corroding in Sample #1. They talk about Sulfur, not sulfur dioxide.

A horse is not a cow and sulfur dioxide is not elemental sulfur.
Sulfur is a solid - a yellow powder
Sulfur dioxide is a gas
 

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