Thought you might enjoy reading the
attached article,
Regards, Frank
* * *
Okay, Frank, you get another award:
The Procrustes Award for stretching the facts to fit the theory.
Meanwhile, since you're interested
in pyrotechnics, check out:
http://waronwar.us
Cheers
Kevin
The Collapse of WTC 1 and 2: A New Theory
F. R. Greening
“Let us never tolerate outrageous conspiracy
theories concerning the attacks of September the 11th.”
George W.
Bush
1.0Introduction
At the time of writing, (March
2007), there are three main theories that claim to explain the collapse
of WTC 1 & 2:
1.
The “official
theory”: The collapse events were natural, gravitationally driven,
processes that were brought on by the localized damage caused by the
aircraft impacts and subsequent fires.
2.
Dr. Steven
Jones’ theory: The collapse events were man-made processes caused by the
timed ignition of pre-planted explosives or incendiary devices.
3.
Dr. Judy
Wood’s theory: The collapse events were man-made processes induced by an
external source of directed energy.
Needless to say, each of these
theories has its supporters and its detractors. Indeed, so much has been
written on the pros and cons of each of these theories that there is
little to be gained in going over all the arguments one more time.
Instead, I recommend to anyone who is not familiar with these theories
to simply go to well-known 9/11 websites such as 911Myths, Debunking911
for arguments supporting theory No. 1; Scholars for Truth (Steven Jones’
site) for support for theory No. 2 and Judy Wood and/or Jim Fetzer’s
websites for support for theory No. 3.
However, if any WTC collapse theory
is to gain full acceptance it must, at the very minimum, be able to
explain certain well-documented phenomena such as:
· Sudden on-set of the
collapse of each tower
· Near free fall descent of
the block of floors above each impact zone
· Pulverization and ejection
of concrete during the collapse
· The completeness of the
destruction of each tower
· Sustained high
temperatures in the rubble pile long after 9/11
Most, if not all, of these phenomena
have been quoted as being problematic in some way to the currently
proposed collapse theories. In this article a new theory of the WTC
collapse is presented – one that involves the use of pre-planted
ammonium perchlorate (AP) based mixtures – that is able to explain these
and other important characteristics of the demise of WTC 1 & 2. In many
respects, the new theory, which I will refer to as the AP theory (or
theory No. 4, if you prefer!), is similar to Steven Jones’ pre-planted
thermite/explosives theory. However, as this report will show, the use
of AP as an incendiary/explosive is preferable to thermite mainly
because it avoids the problems associated with complex wiring and
detonator devices that would have been required to ignite thermite-based
incendiaries or conventional explosives.
2.0The Ammonium Perchlorate-Assisted-Collapse Theory
Background:
Ammonium perchlorate, NH4ClO4,
is a colorless, odorless, compound that is stable at room temperature.
However, when heated to above 300 °C, or subjected to friction or
impact, it becomes violently reactive. In fact, ammonium perchlorate is
a much-used ingredient in explosives, pyrothechnics and solid
propellants such as those used in the space shuttle booster rockets.
The decomposition reactions of
ammonium perchlorate are complex and variable: Cl2, HCl, NH3,
N2O, NO, N2, H2O and O2 have
been consistently observed as major products. The decomposition reaction
is highly exothermic, releasing about 2 MJ/kg of heat energy, and is
accompanied by the production of about 800 liters/kg of gases. The
combustion of ammonium perchlorate in oxygen-rich atmospheres produces a
diffusion flame at about 3200 °C
The decomposition of samples of pure
ammonium perchlorate at 225 °C is 25 % complete after 4 hours. However,
if the ammonium perchlorate is mixed with suitable metal oxide catalysts
the decomposition is accelerated. Among the large number of metal oxides
that have been investigated as AP decomposition catalysts, such as Al2O3,
CaO, Fe2O3 and MnO2, manganese
dioxide is found to be by far the most effective. Thus an
addition of 10 % by weight of MnO2 to ammonium perchlorate
increases the decomposition rate by a factor of about 2. Based on these
properties of ammonium perchlorate / manganese dioxide mixtures, the
following scenario is presented as a new collapse theory:
1. The
Twin Towers were Primed with AP:
Ammonium perchlorate powder,
probably containing up to 10 wt % manganese dioxide and other additives
(e.g. Al, HMX, etc.), was prepared and mixed with one or more of the
five spray-on fire resistive (thermal insulation) materials used in WTC
1 & 2. These materials are identified in NIST NCSTAR 1-6A as: (1)
Blaze-shield Type D, (2) Blaze-shield Type DC/F, (3) Blaze-shield Type
II, (4) Monokote MK-5, and (5) Vermiculite aggregate plaster. In order
to determine where and when these material were applied to
surfaces in the Twin Towers we need to consider the history of the
“passive fire protection” practices employed by the New York Port
Authority during and after the construction of the towers, starting in
1970 and ending in 2001.
On April 13, 1970, New York City
issued a ban on the use of all sprayed on thermal insulations containing
asbestos, the notorious fibrous silicate mineral that was a major
component of Blaze-shield Type D. The use of asbestos-containing
insulation was discontinued at this time at the 38th floor of
WTC 1. In February 1975, a fire occurred in WTC 1 that affected floors 9
to 19 and led to a review of the adequacy of the existing thermal
insulation in the entire WTC. The need to upgrade the passive fire
protection in the Twin Towers was finally addressed in 1995 when, after
yet another study, it was decided to apply a 1½ inch thickness of an
asbestos-free spray-on mineral fiber fire protection material to
selected steel surfaces. Thus, between 1995 and 2001, thermal protection
was upgraded specifically on 18 floors in WTC 1, including floors 92 to
100 and 102; and on 13 floors in WTC 2 including floors 77, 78, 88, 89,
92 and 97. (See NIST NCSTAR 1-6A page xxxvii).
How much thermal protection was
used? A reasonable estimate would be a thickness of 2 cm over an
effective area of 2500 m2 or 50 m3 per floor. If
we assume the material had a density of 400 kg/m3 there
would have been 20 tonnes of thermal protection per floor.
It should be noted that the specific
floor selection would have made on the basis of the need to apply
fire protection material to a particular area. Thus protection would
have been sprayed on areas that were known to be vulnerable to
fire damage. However, in the AP theory, the fire protector
was, in fact, a fire accelerant or pyrotechnic, most probably an
ammonium perchlorate/manganese dioxide mixture blended with a portland
cement-based binder, or something similar. Given the fact that upgrading
of the passive fire protection of WTC 1 & 2 was an on-going project
throughout the late 1990s, a deadly pyrotechnic coating could have been
applied almost anywhere and at any time during this period. If we assume
that the normal cement-based material was “spiked” with 25 wt.% of our
pyrotechnic mixture, up to 5 tonnes of ammonium perchlorate could
have been sprayed onto a designated floor. Furthermore, once
applied to a particular floor, the coating would have remained
undisturbed, unnoticed, and with no loss of potency, until it was
triggered by the events of September 11th 2001.
2.
Boeing 767 Aircraft Strike the Towers and Start Fires
It is documented in the NIST and
FEMA WTC Reports that the aircraft strikes on the Twin Towers on the
morning of September 11th 2001 inflicted major structural
damage to several floors of each tower. NIST’s assessment of the damage
is based on modeling of a Boeing 767 aircraft, weighing about 125 tonnes
and traveling at about 500 mph, crashing into each tower and igniting
about 30 tons of jet fuel. A spectacular fireball was seen after each
aircraft impact and the blast overpressure caused considerable damage to
office furniture, wallboards, ceiling tiles and windows on the impacted
floors. However, it is believed that this over-pressure was
insufficient to have damaged the structural steel support
columns; hence, structural damage that did occur was inflicted
by direct kinetic energy transfer.
On the other hand, if ammonium
perchlorate-impregnated insulation was pre-planted on the upper floors
of the Twin Towers and was subsequently subjected to hard impact, a
violent detonation would have occurred which would have greatly
intensified the energy release compared to a simple fuel-air
deflagration. What is more important, however, is that the protracted
fires that followed the aircraft impacts would have been more damaging
than expected if the upper floors of the towers were primed with
ammonium perchlorate - a potent oxidizing agent that would have been
activated as the surface temperatures in affected areas reached 250-300
°C.
NIST carried out fire resistance
testing of simulated WTC floor (truss) assemblies, (See NIST NCSTAR 1-6A
and 1-6B), using procedures prescribed by ASTM E-119: “Standard Methods
for Fire Tests of Building Construction and Materials.” One of the most
significant findings was that test specimens protected with ¾ in. thick
fire-resistive material reached 300 °C in about 45 minutes at which
point the top chords yielded due to the difference in thermal expansion
of steel and lightweight concrete. However, other tests and/or computer
simulations indicated that the steel
temperatures of WTC 1 & 2 floors and exterior columns were generally
lower than 300 °C.
It is concluded by NIST that
although insulated floors thermally expanded and pushed outwards on the
exterior columns, thereby sagging up to 8 in., the floor sag was
insufficient to pull-in the exterior columns. In view of this finding,
NIST have proposed that thermal insulation must have been displaced by
the entry of the Boeing aircraft into the impact zones of each tower,
namely, floors 94 to 98 in WTC 1 and floors 78 to 83 in WTC 2. This loss
of thermal insulation allowed floor and column assemblies to reach
temperatures in excess of 600 °C. It is also estimated by NIST that
exterior column pull-in was significant above 560 °C at which point the
truss seat bolts sheared off.
Let us now reconsider the NIST
description of the collapse of WTC 1 & 2 in the light of the suggestion
that the passive fire protection coating was spiked with 25 % of an
ammonium perclorate – manganese dioxide (AP) mixture. It is proposed
that three decomposition behaviors would result depending on the local
temperature and rate of heating:
(i)
For slow
heating up to 250 °C: a gradual exothermic
decomposition of the AP would occur.
(ii)
For rapid
heating in the range 250 – 350 °C: a fast
exothermic decomposition of the AP would occur.
(iii)
For rapid
heating to temperatures above 350
°C, or under
impact loading: detonation of the AP would occur.
The fire-resistant coatings in the
Twin Towers were located in covered and relatively inaccessible areas.
Consequently, AP decomposition modes (i) and (ii) would not
have been visible from outside the towers. Nevertheless their effects
would have been highly detrimental to the integrity of floor trusses and
adjacent areas as the following calculation demonstrates:
Mass of steel trough decking per
floor = 16 tonnes
Mass of ammonium perchlorate coating
per floor (See item 1 above) = 5 tonnes
Heat of decomposition of ammonium
perchlorate = 2 MJ/kg
Heat released by the complete
decomposition of 5 tonnes of AP = 10,000 MJ
Heat capacity of iron = 0.45 kJ/kg
Heat required to raise the
temperature of 16 tonnes of steel by 1 °C = 16,000 ´ 0.45 kJ = 7.2 MJ
Hence, the maximum temperature
increase produced by reaction of 5 tonnes of AP = 1390 °C
This would have been enough heat to
melt the steel decking! However, on a cautionary note, the above
calculation is very approximate because it ignores questions of heat
transfer to the steel. Nevertheless, as a first approximation, it
clearly illustrates the potential for major heat damage to the flooring
system by an AP-spiked coating. This degree of heat generation also
provides a mechanism for the formation of the much-debated “molten
steel” at the WTC.
3.
The Twin Towers Collapse in a Shower of Dust and
Debris
The record shows that on the morning
of September 11th, 2001, WTC 1 was impacted by a Boeing 767
aircraft at 8:46 a.m. and collapsed 102 minutes later at 10:28 a.m. WTC
2 was similarly impacted at 9:03 a.m. and collapsed 56 minutes later at
9:59 a.m. The NIST collapse initiation theory for the Twin Towers
involves a gradual weakening and overloading of structural steel members
in the impact damaged, fire-affected zones of the buildings. However, it
is very important to note that the loss of portions of the passive
thermal protection in the fire-affected zones of WTC 1 & 2 is crucial to
the viability of NIST’s theory.
In our new WTC collapse theory the
NIST model is still, in a sense, valid but the need to invoke the
loss of passive thermal protection is obviated by the proposed spiking
of the fire retardant with the potent oxidizing agent ammonium
perchlorate. Thus, far from protecting the buildings from fire
damage, the sprayed-on coating, once activated, would have actually
heated the floor assemblies so severely that catastrophic failures in
susceptible areas such as the truss seats eventually occurred. The
details of this process are controversial, but whatever precipitated the
final collapse of the Twin Towers, the results were rapid and decisive.
And it was during the ensuing 12 - 15 second collapse intervals that the
deadly ammonium perchlorate coating first revealed its presence to the
world in a very dramatic way.
The near free fall descent of the
upper sections of WTC 1 & 2 has been much discussed; so too has the
in situ pulverization of the concrete. While these phenomena are
potentially explicable within a gravity driven collapse scenario, the
overall behavior of the ejected dust and debris was quite remarkable but
is well accounted for by our new collapse theory. First, it should be
recognized that the ammonium perchlorate that is postulated to have been
applied to the upper sections of WTC 1 & 2 would have been activated by
the jet fuel fires prior to collapse initiation and, as
the AP decomposed, it would have made the affected surface coatings very
hot and friable. In addition, gas generation associated with the
decomposition reaction (800 liters per kg) would have made the coatings
exfoliate so that falling sections of coated material would have left
pronounced trails of dust. Furthermore, since AP detonates under
moderate impact loading, coated building sections falling onto the
floors below would have set off explosions resulting in violent
ejections of pulverized material, as was
observed during the collapse of WTC 1 & 2.
We have previously proposed that up
to 5 tonnes of ammonium perchlorate was applied to selected upper level
floors in WTC 1 & 2 and now suggest that ~ 15 floors were treated with
this chemical so that the total loading of ammonium perchlorate
was about 75 tonnes per tower. If 50 % of the available AP
reacted before or during the collapse of each tower, ~ 30 million
liters of hot and potentially corrosive gases such as HCl, Cl2
and NO would have been released by the time the rubble pile was formed.
In any case, the remaining 50 % of the AP would eventually also react in
the smoldering rubble pile, as we shall now discuss.
4.
The Rubble
Pile Stays Hot and Cooking for Months after 9/11
The massive rubble pile that
formed at Ground Zero as a result of the collapse of WTC 1 & 2 was
notable in many ways but in the present context we need to focus on only
two features of the pile: its sustained high temperatures and its toxic
emissions. Elevated temperatures (over 600 °C – see below) were observed
at many locations within the rubble pile and remained high for several
months after 9/11. These sustained high temperatures are indicative of
exothermic chemical reactions within the pile that need to be explained.
Similarly, while toxic emissions from a burning building are to be
expected, the chemical make-up of the emissions measured at, or near,
Ground Zero was highly unusual. Nevertheless, as we shall discuss below,
residual ammonium perchlorate at Ground Zero offers a convenient
explanation of both the sustained high temperatures, and the gaseous
emissions from the rubble pile.
The Sustained High Temperatures:
In an article in the
October 2003 issue of Chemical & Engineering News, L. Dalton has
summarized the progress of the fires and the associated temperatures
within the WTC rubble pile:
“The fires, which began at over 1,000 °C, gradually
cooled, at least on the surface, during September and October 2001.
USGS's AVIRIS measured ground temperatures when it flew over the WTC
site on Sept. 16 and 23. On Sept. 16, it picked up more than three-dozen
hot spots of varying size and temperature, roughly between 500 and 700
°C. By Sept. 23, only two or three of the hot spots remained, and those
were sharply reduced in intensity, researcher Clark said.However, Clark
doesn't know how deep into the pile AVIRIS could see. The infrared data
certainly revealed surface temperatures, yet the smoldering piles below
the surface may have remained at much higher temperatures. "In
mid-October," said Thomas A. Cahill a retired professor of physics and
atmospheric science at the University of California, Davis, "when they
would pull out a steel beam, the lower part would be glowing dull red,
which indicates a temperature on the order of 500 to 600 °C. And we know
that people were turning over pieces of concrete in December that would
flash into fire--which requires about 300 °C. So the surface of the pile
cooled rather rapidly, but the bulk of the pile stayed hot all the way
to December."
NIST estimates that the
heat release rate of the fires in WTC 1 & 2 in the time period just
before the collapse of these buildings was about 0.5 gigawatts. We will
assume that burning material and fresh combustible live load material
was transferred en masse to a depth several meters below the top
of the rubble pile where it continued to burn. Initially the heat flux
near the top of the rubble pile would have been as high as 100 kW/m2
with an inferred combustion rate of about 25 kg/s. However, as the
initial oxygen supply from air pockets within the rubble pile dwindled,
the combustion rate and heat flux would have declined until it was
reduced to a smoldering state.
Smoldering is a
well-studied and quite reproducible phenomenon. It is observed in
man-made situations such as garbage dump or tire-pile fires, and in the
natural environment in forest fires. Smoldering is usually quantified in
terms of the velocity at which the char front advances, as in the
well-known example of a cigarette. In stationary air, the smoldering of
compressed cellulose-based material proceeds at very consistent rates in
the range 10-3
cm/s. Thus we see that, in the period immediately after 9-11, a zone
existed several meters below the top of the rubble pile where
combustible material burned in a self-sustaining, smoldering condition.
Furthermore, in the presence of an adequate supply of oxygen, this
smoldering combustion could have continued until the supply of “fuel”-
office furniture, paper, textiles and plastic materials - was exhausted.
However it is important to note that this smoldering mass could only
have sustained temperatures up to about 350° C and we know the
rubble pile was hotter than this!
This picture changes
dramatically if we assume that un-reacted ammonium percholrate was
present in the rubble pile. In item 3 above, we have already suggested
that up to 50 % of the initial loading of AP could have found its way
into the rubble pile; for two towers this would have been about 75
tonnes of un-reacted AP. Now, because the thermal decomposition of
ammonium perchlorate releases about 2 MJ/kg of heat energy, a total of
150 GJ would have been available from this source. Furthermore, because
the smoldering material in the rubble pile was already capable of
generating and sustaining temperatures of 350 °C, the conditions in the
pile would have been quite sufficient to initiate the AP decomposition
reaction in localized areas. What is also very significant is that
water, (which was in great supply during recovery operations at Ground
Zero), is known to “rejuvenate” partly decomposed AP, (See Proc. Roy.
Soc. A227, 115, (1954))
It is, of course, quite
difficult to estimate the temperature that a rubble pile “spiked” with
AP could attain but we note that temperatures in excess of 600 °C have
been recorded at the surface of “burning” AP (See Chemical Reviews Vol.
69, 551, (1969)). However, this is just the beginning of the heating
effects of pre-planted AP in the Twin Towers because we need to also
consider the fate of the gaseous decomposition products of AP,
especially the reactive species oxygen, chlorine, hydrochloric acid,
nitric oxide and ammonia. Alone, or in the presence of water vapor,
these gases would be extremely reactive towards metals such as iron and
aluminum that were present in the rubble pile. For example, the
reactions of iron with the O2, HCl and Cl2
released from the thermal decomposition of 1 kg of ammonium perchlorate
would release about 3 MJ of heat energy.
Gaseous Emissions from
the Rubble Pile
To establish supporting
evidence for an ammonium perchlorate theory it is helpful to look for
“chemical signatures” of the presence of ammonium perchlorate in the
rubble pile. This requires careful scrutiny of the available data on
gaseous emissions at Ground Zero. For example, consider the Report on
Air Sampling Near the World Trade Center Site: New York State Department
of Health, October 30 & 31, 2001.” In this document we find that air
sampling of the smoke plume on the rubble pile over one month after 9/11
measured 33.9 mg/m3 of HCl as well as 2.24 mg/m3
of HNO2 and 12.28 mg/m3 of HNO3. The
presence of these acid gases in the air above the WTC rubble pile at
this time is consistent with the emission of
Cl2, HCl, N2O, NO, and H2O
from the slow decomposition of ammonium perchlorate.
Prof. T. A. Cahill at U.C.
Davis has also published data on aerosol samples collected at or near
Ground Zero in October 2001. (See Aerosol Science and Technology 38,
165, (2004)) Among the data reported by Cahill is a mass spectrum of 5 –
2.5 mm particulate collected from within the smoke plume on Varick
Street. In agreement with the results noted above, the mass spectrum’s
three strongest peaks reveal the presence of Cl, NO2 and NO3.
However, Cahill suggests that the detection of chlorine may be explained
by “ the relatively large chlorine inventory in the WTC buildings
from plastics, including the ubiquitous PVC, and chlorine-bleached
paper.” Let us therefore briefly review data on chlorinated species
at the WTC in relation to studies of the behavior of chlorine-containing
materials such as PVC in building and other related fires.
Analytical data reported by
the US EPA derived from air monitoring at, or near, Ground Zero in the
period September 2001 to May 2002 show that many chlorinated organic
species were present at significant levels up to December 2001. These
included aliphatic species such as chloroform, chloroethane and
di-chloroethane as well as the aromatic compounds chlorobenzene and di-chlorobenzene.
The maximum concentrations observed for these and related species are
given in Table 1. The compounds listed in Table 1 are arranged into two
groups: chlorinated species produced by the thermal degradation of PVC
and chlorinated species that are not derived from PVC
decomposition. The PVC-derived designation was arrived at from published
data on the thermal decomposition of PVC, (See for example: Journal of
Polymer Science 12, 737, (1974)). Apart from HCl, which is indeed a
major product of the thermal degradation of PVC, the major decomposition
products from heating PVC in the temperature range 300 – 500 °C are:
benzene, toluene, ethylbenzene, chlorobenzene, di-chlorobenzene and
tri-chlorobenzene. As Table 1 shows, all of these species were observed
in the air at Ground Zero. Furthermore, the relative abundances of the
PVC-derived compounds in Table 1 are consistent with literature data on
the thermal decomposition of PVC.
Table 1. Major Chlorinated and Related Organic
Species Observed in the Air at Ground Zero (EPA Data: September to
December 2001)
|
Source
Type
|
Compound |
Maximum Concentration
(ppb) |
|
PVC Degradation
Product |
Benzene |
180,000 |
|
Toluene |
74,000 |
|
Ethyl Benzene |
67,000 |
|
Chlorobenzene |
1,900 |
|
Di-chlorobenzene |
1,540 |
|
Tri-chlorobenzene |
57 |
|
Non-PVC
Origin |
Chloroform |
2,000 |
|
Chloroethane |
3,200 |
|
1,2
di-chloroethane |
2,100 |
|
Tri-chloroethane |
1,300 |
|
Tetra-chloroethane |
140 |
However, the most
interesting feature of the data in Table 1 is the fact that the
non-PVC-derived chlorinated species are more abundant than the
PVC-derived species. This clearly demonstrates the presence of
another major source of chlorine, above and beyond “the ubiquitous
PVC” previously postulated by Prof. Cahill as the most likely source
of the elevated levels of chlorine in air samples collected at Ground
Zero up to December 2001.
An alternative source of
chlorine suggested by Prof. Cahill, namely chlorine-bleached paper, may
also be ruled out as a major contributor to chlorine emissions at Ground
Zero. Thus, while there certainly was certainly a large amount of paper
in the Twin Towers, a reasonable upper limit would be 500 kg per office
´ 100 offices per floor, or 50 tonnes of paper per floor. However, paper
typically contains no more than 0.5 wt. % of chlorine so that each floor
would have contributed a maximum of only 250 kg of chlorine to the total
inventory of chlorine in the Twin Towers. This should be compared to a
chlorine contribution of about 1500 kg per floor if ammonium perchlorate
was pre-planted to the concentrations we have previously suggested.
In conclusion we note that
a full consideration of all the potential sources of fluorine and
chlorine in the WTC shows that CFC refrigerants such as Freon-22, (chlorodifluoromethane,
CHClF2), used in the central air conditioning system, as well
as the floor-specific fire suppression agent Halon 1301, (bromotrifluoromethane,
CBrF3), were significant additional sources of Cl and F.
3.0Summary and Conclusions
(with Physicochemical Evidence for Molten Iron)
The effect of adding the
pyrotechnic agent ammonium perchlorate, NH4ClO4
(AP), to the thermal insulation/fire-protective coating used on the
upper floors of WTC 1 & 2 has been considered. It is noted that
exothermic decomposition of an AP “spiked” coating, initiated at ~ 300
°C, would have had catastrophic consequences to the integrity of the
buildings at or above the impact zones in each tower. The most
detrimental consequences of the presence of kilogram quantities of the
energy-rich oxidizing agent ammonium perchlorate would have been in
fire-ravaged areas of WTC 1 & 2 where rapid “shock-heating” of floor
assemblies would have lead to:
(i)
Differential thermal expansion
causing buckling or fracture of floor elements
(ii)
Complete collapse of entire
floor sections
(iii)
Explosive spalling and
“powderizing” of the concrete.
(iv)
Melting of the corrugated
steel floor pans
With the possible exception
of item (iv), these four phenomena are well-known features of the
collapse of WTC 1 & 2. But let’s consider the evidence for item (iv) and
the crucial question of molten steel in the WTC rubble pile at Ground
Zero in more detail. While this topic has been debated on many 9/11
websites, nearly all of the arguments I have seen rely on visual
sightings of “molten metal” in the rubble pile - information drawn from
eyewitness accounts recalled by recovery workers. This type of anecdotal
evidence has been strongly criticized for its lack of scientific
credibility. Remarkably, however, there is some crucial
scientific evidence for the presence of molten iron or steel in the
pulverized remains of WTC 1 & 2 that has apparently been completely
ignored by 9/11 researchers.
I am referring to the
observation of micron-sized iron spherules that have been
seen in many WTC dust samples. These spherical particles are
direct physical evidence that the iron within the particle was molten at
the time the particle formed.
Each of the references
below specifically mention the detection of iron spherules in WTC
dust samples (and in most cases also provide electron micrographs of
the particles in question). Reference 1 includes two such micrographs
labeled IRON-03-IMAGE and IRON-04-IMAGE. Reference 2 discusses which WTC
particles could best be used as signatures of WTC dust; iron spheres
were considered and rejected only because they were not found in
all indoor dust samples. In reference 3 we read on page 17: “Various
metals (most notably iron and lead) were melted during the WTC event,
producing spherical metallic particles.” And finally in
reference 4 we find a micrograph of a spherical iron particle and the
comment that WTC dust contains evidence for “heat effected particles,
including spherical particles.”
1.
H. A. Lowers
et al. “Particle Atlas of World Trade Center Dust.” USGS
Open-File Report 2005-1165, (2005)
2.
Various
authors: “U.S. EPA Response to the Peer Review of the U.S.
Environmental Protection Agency’s Final Report on the World Trade Center
Dust Screening Study.” Page 28, (December 2006)
3.
R. J. Lee et
al. “Damage Assessment 130 Liberty Street Property: WTC Dust
Signature Report on Composition and Morphology.” Issued December
2003.
4.
S. R. Badger
et al. “World Trade Center Particulate Contamination Signature Based
on Dust Composition and Morphology.” Microscopy and Microanalysis 10
(Supplement 2), 948, (2004).
The formation of spherical iron
particles has been well documented and researched for steel making
processes, (See for example: Steel Research 64, 23, (1993) and Steel
Research 72, 324 (2001)). Iron spheres in the 30 mm to sub-micron range
are typically seen in the dust-laden off-gases produced by molten steel
and are believed to be formed by the ejection of metal droplets when the
liquid metal degasses.
In seeking an explanation of the
formation of iron spherules during the destruction of WTC 1 & 2 it is
significant that samples of WTC dust have an additional chemical
signature - an enrichment of zinc. Data for iron and zinc
in WTC aerosol samples have been presented by S. Qureshi and co-workers
in Atmospheric Environment 40, S238, (2006). We first note that
concentrations of these elements in PM2.5 aerosol collected
in New York City prior to 9/11 were about 100 ng/m3
for iron and less than 20 ng/m3 for zinc. Qureshi’s data show
that on September13 2001 the PM2.5 iron concentration was 127
ng/m3 and the zinc concentration was 217 ng/m3,
i.e. airborne zinc concentrations were about ten times higher than
normal. Qureshi’s data also show that both iron and zinc concentrations
in New York’s 2.5-micron dust peaked in early October 2001 with iron at
370 ng/m3 and zinc at a remarkable 1028 ng/m3.
These observations are consistent with iron and zinc data reported by
the EPA for WTC air monitoring samples collected in the same post-9/11
time period.
Why was
so much zinc dispersed into the air above Ground Zero? In order to
answer this question we need to consider sources of zinc in the Twin
Towers. A review of the construction materials in these buildings shows
that the galvanized 22-gauge corrugated sheet steel, used for the
decking that supported the floor concrete, was a major source of zinc.
Given that 22-gauge galvanized steel has a coating of about 50 mm of
zinc on a 1 mm sheet of metal comprised of ~ 98 % iron, we may use our
previous estimate of 16 tonnes for the mass
of steel decking per floor to conclude that there was about 1.6 tonnes
of metallic zinc on every floor in WTC 1 & 2.
We have shown in the first part of
this article that if some of the thermal insulation that was applied to
floor assemblies in the Twin Towers was spiked with 25 % by weight of
ammonium perchlorate and subsequently exposed to jet-fuel fires, it
would have heated the steel decking to ~ 1390 °C. Now, since the
boiling point of zinc is 908 °C, this degree of heating of a floor
assembly would have been sufficient to vaporize the zinc in the
galvanized steel!
To conclude: we have shown that an
AP collapse theory accounts for all four processes that collectively led
to the observed level of destruction to WTC 1 & 2, namely: the buckling
and fracture of floor elements; the collapse of entire floor sections;
explosive spalling and “powderizing” of the concrete; melting of the
floor pans. As an aside, we note that the addition of ammonium
perchlorate to the thermal insulation on the upper floors of the Twin
Towers comes very close to being the perfect crime. The deadly AP-spiked
concoction would have been almost identical to the un-spiked coating; it
could have been sprayed on selected surfaces with impunity; it required
no elaborate detonator devices to be activated – moderate heating worked
just fine. And finally, because AP decomposes to gaseous products, it
leaves no telltale residues. Of course, I haven’t proved
that AP was used in the Twin Towers, but to end with a famous quote:
“How often have I said
to you that when you have eliminated the impossible, whatever remains,
however improbable, must be the truth……..”
The Sign of Four by Arthur Conan Doyle
F.R. Greening, March 15th,
2007