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6.0) FIRE and SMOKE:
(page 2 of 6)
6.13.h) Steel and Metal Compliance:
Structural steel and metal building components
shall meet the minimum structural requirements as described in the
International Building Code
or the
NFPA
5000 Building Construction & Safety Code after they have
been mitigated or restored.
Steel decks or formed steel after mitigation or restoration
procedures shall meet the minimum paint, enamel or other
approved protection requirements described in national and
local adopted building codes, or industry accepted standards.
6.14) Surfaces Conditions: Surfaces should be pre-inspected before
proceeding with the mitigation or neutralizing of the surface. The inspection
of surfaces should include both pre-existing conditions and
post-fire conditions.
The pre-existing condition of
components and contents could be controversial at
times, and all pre-existing conditions should be noted in
writing and photographed.
6.14.a) Post-Fire Conditions: Post-fire
damages to components and contents would be caused by smoke,
soot, heat and moisture. Secondary damages would be mold
(fungi) and corrosion (rust).
6.14.b) Pre-Existing Conditions:
Pre-existing
condition to components and contents would be
scratches, dents and tears, as well as normal wear and usage.
6.15) Carbon Dioxide: Organic
materials such as; wood, coal, oil, lime, foods and
inorganic materials such as;
nylon,
plastics, etc. contain
hydrocarbons. The combustion by-product of hydrocarbons is
carbon dioxide that dissolves in water to form carbonic acid.
Carbonic acid is considered moderately corrosive.
When
carbonic acid is present, the neutralization process of
vulnerable materials should commence immediately. Carbonic
acids although not as corrosive as hydrochloric acid, will
accelerate the oxidation of metals prematurely through
reduction.
6.16) Polyvinyl Chloride (PVC):
Polyvinyl chloride (PVC) is used extensively in
the manufacturing of building components and contents as
described in
Section 6.16.a.
The by-product of
decomposed PVC is
hydrogen chloride (HCl) and readily dissolves
in water through a process called
hydrolysis to form
hydrochloric acid with the same formula (HCl). HCl creates a
highly corrosive reaction with metals and starts deteriorating
the metal surface on impact. Lead gases and soot could be
produced when PVC products contain lead as a
stabilizer as
described in
Section 6.16.b.
Hydrogen chloride gases react with metals to
stimulate corrosion when the metal temperature drops below the
acid dew point of the gas, causing hot acidic condensates to
form, which are highly corrosive to carbon steels. The
thermal
expansion of metals can allow vapors of hydrogen chloride gases
to penetrate the outer layer of the protective coating, and the
metal itself.
The effects of PVC on metal surfaces is not
readably noticeable and can take up to 2 to 4 weeks before
oxidation/corrosion is visible.
Stainless steel is
vulnerable to hydrogen chloride as described in
Section
6.17.b.
Photo 6-16-A shows indirect heat and hydrochloric acid
damages on a corrugated metal roof deck coated with an
iron
oxide primer. The photo in 6-16-B shows atmospheric
heat and hydrochloric acid damage on a corrugated metal roof
deck coated with a silico-chromate primer. Both metal roof
decks were located within the same facility, where the
fuel source contained PVC building components, PVC contents,
nylon clothing and nylon carpet.

Photo 6-16-A
Iron Oxide Coated Metal Deck
Source: William Yobe & Associates

Photo
6-16-B
Silico-Chromate Coated Metal Deck
Source: William Yobe & Associates
Note: The silico-chromate coated
metal deck shown in Photo 6-16-B although rusting is not as deteriorated due to less heat
and the chromium alloy found in silico-chromate primers, which
offers moderate corrosion protection. The period (time frame)
of the
corrosion shown in Photos 6-16-A and 6-16-B was
four weeks after a fire.
Photo 6-16-C
shows hydrochloric acid and carbonic acid damages on heavy
machinery 15 days after an industrial fire, and the photo in 6-16-D shows
steel stock that had a coating of factory applied oil that
started to show rust formation in 7 days.

Photo 6-16-C
High Alloy Machinery
Source: William Yobe & Associates

Photo 6-16-D
Corroded Steel Stock
Source: William Yobe & Associates
When hydrogen chloride and water are present, the neutralization
of the affected surfaces should commence immediately.
Hydrogen chloride resins and gases are corrosive
and toxic, and could be present for days after a fire.
When PVC is a known fuel source, metal surfaces should be
neutralized and receive a protective coating of
petroleum jelly,
vegetable oil
or equal to protect the surface from acid
off-gassing.

Tarry Soot Formation (PVC)
Source: William Yobe & Associates
Photo 6-17-C
6.16.a) Components Containing PVC: PVC
is used in the manufacturing of a large spectrum of building
components and content furnishings. The building
construction industry is
the second largest consumer of polymerized plastics.
Listed below are some items that can contain PVC:
Electrical: Wire insulation, conduit and fittings, J-boxes and device boxes, circuit breakers, receptacles,
switches, light fixtures, etc.
Plumbing: Pipe and fittings,
valves, pumps, faucets, supply lines, bath tub, shower enclosures, etc.
Flooring:
Vinyl base board, stair treads, tile (VCT), inlaid and one piece vinyl, nylon carpet, etc.
Appliances: Refrigerators (both in and out), dish washer, cloths washer, dryer, etc.
Building components: Windows,
doors, cabinets, shelving, casing and baseboard, siding, shutters, mail boxes, wall accessories, wallboards, insulation,
etc.
Contents: Chairs, tables, place settings, cups and plates, sporting goods, toys, stereos, computers and
paraffin wax products, etc. Clothing, such as nylons,
polyester, etc.
6.16.b) Lead and Cadmium in PVC: Although
not used in all products made from PVC, some PVC products are
made with lead and cadmium as a stabilizing additive, which are
labeled as hazardous substances per the
ATSDR and the
EPA.
Other stabilizers used in the manufacturing of
PVC components are
barium,
calcium,
zinc and
tin, while
cadmium
is not commonly used today.
PVC's, when stable do
not produce any known toxic substances and should not present a
health threat.
The decomposition of PVC during a fire could possibly emit lead
or cadmium by-products within the smoke and soot, which could be
distributed throughout a structure and onto its contents.
Since the determination of whether decomposed PVC’s contain lead
or cadmium is not noticeable, items such as; children's toys,
silverware, flatware and glassware should be tested for lead and
cadmium, and properly neutralized or disposed.
6.17) Mitigation Procedures, When Carbon Dioxide
and/or PVC is a Known Fuel Source: When
carbon dioxide or polyvinyl chloride (PVC) is a known fuel
source, the testing, confirmation and neutralizing of susceptible
metal structural components and metal contents should commence
immediately.
Combustion will produce three states of matter: solid, liquid
and gases. Since smoke colors can be white, gray, brown or
black, their color should not be used as an indication of the
soot’s acidic nature.
Mitigation should include, but not be limited to the following:
Structural Components:
- Door and cabinet hardware, hinges, knobs and pulls
- Plumbing faucets, trim, valves, and supply lines
- Bath tubs and shower surrounds
- Bathroom and kitchen wall accessories, chrome or brass
- Built-in
appliances,
chrome, painted surfaces,
electrical motors, etc.
- Light fixtures, ceiling and wall
- Electrical
device plates, (switch & receptacle) brass,
chrome, steel, porcelain, etc.
- Electrical service panel
- Hot water tank
-
HVAC
systems (furnace. A/C, etc.)
- Glass, windows, doors, etc.
- Structural
steel, I-beams, tele-posts, etc.
Contents:
- Exposed glass, porcelain, mirrors, etc.
- Metal picture frames
- Brass items, beds, lamps, candle holders, etc.
- Hard furniture, drawer pulls, hinges, etc.
- Upholstery, should be vacuumed and dry sponged.
If the soot has a tarry substance, dry
sponging
should be avoided
6.17.a) Metals: Ferrous
and non-ferrous metals are affected by hydrogen chloride and
hydrochloric acid, and would include
stainless steel and
galvanized metals.
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6.17.b) Ferrous Metals: Ferrous
metals are carbon,
alloy, stainless and consist mainly of iron.
Alloy and stainless steels contain additives such as;
aluminum,
chromium,
copper,
nickel, zinc, etc. that increases the
corrosion resistance of metals.
Silicon is added to metal to
increase strength, while the corrosion resistance of steel
increases when its
chromium content is 12% or higher.
Hydrogen chloride gases will accelerate corrosion when the
temperature of the hydrogen gases reaches 500º F to 1000º F and
increases considerably when its temperature reaches 1200º F.
Photos 6-17-A and Photo 6-17-B represent a metal roof deck
impacted with hydrogen chloride gases that were over 2000º F per
the fire report. Photo 6-17-A shows
the metal roof deck after it was cleaned with a 13 pH detergent,
using an abrasive cleaning sponge. Photo 6-17-B represents the same metal roof deck
6 months later.

Corroded
Metal Deck after 13 pH Degreaser Cleaning
Source: William Yobe & Associates
Photo 6-17-A

Metal Deck in Figure 6-17-A
6 Months after Cleaning With a 13 pH Degreaser
Source: William Yobe & Associates
Photo 6-17-B
Note: The
powdered rust formation confirms the persistent corrosion
reaction of hydrochloric acid after using a high
pH detergent.
This confirms the need of an
ionic
based chemical or vigorous agitation to un-align the formation
of the metals’ molecules to their pre-right angles.
Stainless steel is vulnerable to chlorides through the breakdown
of the steels’ passive film causing staining and pitting.
Galvanized (zinc) coated steel, although non-corrosive, will
breakdown through
hydrolysis and rust when wet/moist for a
considerable amount of time when exposed to hydrochloric acid.
When removing fire residues from metal surfaces,
the pre-solvent-mechanical removal procedures described in the
NIDR Guidelines for Fire and Smoke Damage Repair could apply.
The NIDR Guidelines also state the mechanical removal of fire
residues does not guarantee neutralization or removal of acids,
which may require additional treatments. The recommended NIDR
mechanical removal techniques are outlined in
Table 6-B.
Procedure
|
Aggressiveness
|
|
Compressed air |
Mild |
|
Vacuum w/ brush Attachment |
Mild |
|
Feather duster or similar device |
Mild |
|
Soft brushes |
Mild |
|
Sticky tape, tack cloth |
Mild |
|
Cellular rubber (dry sponge) |
Moderately Aggressive |
|
Dry terry towel |
Moderately
Aggressive |
|
Treated cloths |
Moderately
Aggressive |
|
Malleable (putty-type) cleaner |
Moderately Aggressive |
|
Art-gum eraser |
Aggressive |
|
Stiff brushes |
Aggressive |
|
Abrasive powders |
Moderate to Aggressive |
|
Abrasive papers, steel wool |
Very Aggressive |
|
Scrapers |
Very Aggressive |
|
Machine buffing, polishing |
Moderate to Aggressive |
|
Grit blasting, various media; Ground corn
cobs, Soda, CO2, Sponge, Glass beads, Sand, etc. |
Aggressive to
Very Aggressive |
Some Techniques for Mechanical Removal of
Residues
© ASCR Reprinted with the permission of the
Association of Specialists in Cleaning and Restoration
Millersville, MD
Table 6-B
6.17.c) Non-Ferrous Metals: Non-ferrous
metals such as; aluminum, copper and zinc are non-corrosive.
Aluminum is resistant
to corrosion through the oxide film that forms on its
surface. When hydrogen chloride gases impact
aluminum, the
white oxidation that forms on the surface of the metal could
produce
benzene (C6H6).
Copper is
mined ore and is resistant to corrosion. Moisture and oxygen
will turn
copper from red/orange to red/brown. Copper, when
exposed for long periods will produce a green film called
patina, hydrogen containing chlorides will accelerate copper to
the patina stage.
Brass is an alloy containing copper and
zinc.
High tensile strength brass contains small amounts of iron,
magnesium, aluminum, lead and tin. Naval brass contains more
than 1% tin and is highly resistant to sulfur corrosion.
6.17.d) Small to Medium Metal Surface Mitigation,
When PVC is a Known Fuel Source: Building
components such as; door hardware, metal doors, plumbing
fixtures, electrical panels, light fixtures, furnace, hot water
tank, etc. should be neutralized with an ionic cleaner. Then
all cleaning media should be rinsed with clean mineral free
water and a coating of
petroleum jelly,
vegetable oil or equal
should be applied if corrosive off gases are present.
When tarry soot is
present, degreasers could be required.
6.17.e) Large Metal Surface Mitigation, When PVC is a Known Fuel
Source:
Several factors enhance oxidation and corrosion
on metal surfaces after fire and smoke losses when PVC is the
fuel source, those factors being; temperature,
thermal
expansion,
alloying, moisture and oxygen.
Corrosion caused from the reaction of hydrochloric acid (HCl),
unlike normal rusting does not stop when the moisture or oxygen
source has been corrected. Corrosion when produced from HCl
rearranges the molecule make-up of the metal, and is
irresolvable in some instances unless treated with the correct
chemical or process.
An example of repeated corrosion due to hydrochloric acid is
shown in Photo 6-17-C and Photo 6-17-D.

Repeated Corrosion Due to PVC
Source: William Yobe & Associates
Photo
6-17-D
Note: the corrosion bled through the tarry soot in Photo 6-17-D
after it cured, while Photo 6-17-C was taken 6 months before
Photo 6-17-D.
The powdered rust formation on corroded steel is crystallization
from salt. For acids contain the ester of salt and the orange
color is the result of the pigmentation of the iron.
The mitigation of large metal surfaces such as; metal roof
decks, trusses, I-Beams, etc. would result in a
complete restoration of the surface
if neutralized before corrosion sets in.
When neutralizing large metal surfaces before corrosion has
started, the methods used should reduce the acid content of the
metal to the minimum standards set-forth in SSPC-SP 12/NACE No.5
as outlined in Table 6-C.
|
Contaminate |
Reduction Level |
|
Soluble Sulfate |
17 to 50 mcg/cm2 |
|
Chloride |
7 mcg/cm2 |
|
Soluble Ferrous Ion |
10 mcg/cm2 |
Contaminate Reduction Levels
Source: SSPC &
NACE
Table 6-C
After a metal surface has been restored of its over-voltage, the
metal surface should receive a coating of primer or paint to
prevent normal electrochemical corrosion (rusting).
Large metal surfaces can be mitigated or restored
using (CO2) dry ice blasting, soda ash blasting, pressure
washing, high-pressure washing or blast-cleaning.
Pressure washing: Ionic
cleaners and detergents can be applied with a
pressure washer to
neutralize hydrogen chloride or hydrochloric acid. Basic
residential pressure washers produce 2.0 to 5.0 gallons per
minute and after pressure washing, airmovers and
dehumidifiers
could be required to prevent secondary damages such as
microbiological growth, nominal electrochemical corrosion and
flash rusting.
When metal surfaces have accelerated rust due to HCl, commercial
grade pressure washers that produce 4 to 14 gallons per minute
would be required per the Steel Structures Painting Council (SSPC).
Excessive runoff water
should be collected and disposed per EPA and state regulations.
Surfaces receiving ionic cleaners should be rinsed with clean
mineral free water.
C02:
Dry ice blasting is an acceptable means of removing hydrogen
chloride or hydrochloric acid before oxidation and corrosion is
present. Cold jet blasting / cleaning systems, the application
machine used to force pellets through a regulated nozzle are
capable of cleaning or blasting a surface. This application
system meets
EPA,
USDA and
FDA guidelines since the dry ice
pellets instantly vaporize without generating secondary waste.
Manufacturers of
dry
ice blasting systems state their systems will not effectively
remove items such as heat treat scale, mill scale and scale
corrosion. Although dry ice blasting systems will remove soot,
toxic residues, mold and biofilm buildups such as;
listeria and
salmonella, and is safe to use in the food, automotive and
nuclear industries
Soda: Soda
(baking) ash can be used to remove hydrogen chloride and hydrochloric
acid before oxidation / corrosion is present, as well as after
oxidation/corrosion has started. This is possible based on the
varying abrasives available. Plain soda ash when used with
micro blasting systems could be used on fragile electronics,
while soda ash containing heavy grit will remove rust and paints
from steel substrates. This application meets EPA, USDA and FDA
guidelines since soda ash is a non-toxic organic food source.
Soda ash is applied dry or wet. Wet applications could require
a second application of clean mineral free water to remove soda
ash residue. Based on the type and condition of the surface
being blasted, media waste should be cleaned-up and disposed
accordingly. Baghouse type structures could be utilized with
airmovers to catch soda ash media waste.
Blast-cleaning: Metal
surfaces that have repeated corrosion due to HCl and have set
for an amount time could require pressure washing with an
ionic-cleaner, then blast-cleaning. The degree of the corroded
surface, intended surface results and the intended coating would
determine which media and applicator would be appropriate.
Blasting media such as
sand, steel, iron, etc. are available in varying grits and
applied via compressed air or rotary-type blasting equipment.
Both offer varying surface preparation through the type, shape
and size of the media, as well as the speeds they are applied.
The following blasting surface degrees are available:
White metal clean: Is when no visible
residues remain after blasting, and the surface has a
uniformed color.
Near white clean: Is when traces of
residues and mill scale is present after blasting.
Brush-off clean: Is
the removal of loose residues.

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