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Fastener Corrosion in ACQ and Other “Next Generation” Treated Lumber

March 22, 2005

Pathways to
Professionalism
Proceedings of the
RCI 20th International
Convention & Trade Show
Miami Beach, Florida
March 31 – April 5, 2005
© Roof Consultants Institute
1500 Sunday Drive, Suite 204 • Raleigh, NC 27607
Phone: 919-859-0742 • Fax: 919-859-1328 • http://www.rci-online.org
Fastener Corrosion in ACQ and Other
“Next Generation” Treated Lumber
By Heinz Wieland
Presented by Gary P. Martini
SFS Intec • Wyomissing, PA
ABSTRACT
The EPA has mandated changes in the composition of wood preservatives for pressure
treated lumber. These changes eliminate the use of arsenic, but allow the introduction
of other, more corrosive compounds. Steel fasteners are at risk. This presentation
will discuss the corrosive nature of “next generation” pressure treatments
and the various fastener solutions for this problem.
SPEAKER
GARY P. MARTINI is the vice president of sales and marketing for one of the world’s largest manufacturers
of fastening systems for commercial roofs. SFS Intec employs 60 people in engineering and design
and dedicates these resources to solving the problems of the industry such as this one. The issue of ACQ
and similar pressure treatment systems has been a focus of the company for the past year.
Prior to joining SFS Intec, Mr. Martini served for ten years as the manager of alloy products for a major
steel producer, focused on the development of corrosion- and abrasion-resistant grades of steel for the construction
and defense markets.
Martini and Wieland – 107
Martini and Wieland – 109
PROBLEM DEFINITION
Building materials, including
roofing products, trim attachments,
and gutters are often connected
to pressure-treated lumber
by metallic fasteners such as
nails or screws. Like most metalbased
components, these connectors
and fasteners are susceptible
to corrosion.
Corrosion is a time- and environment-
dependent process. Unfortunately,
corrosion is also an
extremely complex process. It is
common for the causes of corrosion,
and thus the methods of corrosion
prevention, to be
misunderstood and thereby
misapplied. The very
nature of the supply
chain for components to
the building construction
industry often feeds this
trail of misinformation.
This leads to well-intentioned
applicators installing
components that are
doomed to a usable life far short
of written warranties or implied
system life. Fastener manufacturers
offer only comparative information
based upon experiences in
like materials. Lumber treaters
transfer the onus for knowledge to
the applicator. Trim or membrane
manufacturers rely on the knowledge
and experience of fastener
manufacturers. As a result, in
practice, proper science is never
applied by any party to back up
guarantees implied to building
owners.
The very reason that lumber is
preservative pressure treated is to
avoid premature failure due to
insect infestation and rot deterioration.
To prevent failure of a
lumber or timber structure, both
the wood material and the connection
devices have to be stable
over the intended period of service.
Wood preservative treatment
is an old process and there is significant
practical experience with
the behavior of metal fasteners in
treated lumber.
The reason for the renewed
debate is an EPA- (Environmental
Protection Agency) mandated
change in lumber and timber
preservative materials. The traditional
preservative CCA has been
replaced to a great extent due to
health and environmental concerns.
CCA is an abbreviation for
copper chrome arsenate. Chromium
and arsenic are harmful both
to human health and environment.
For purposes of this discussion,
this is stipulated even
though when properly applied
and installed, the composite CCA
has a rather low potential for
harm. Key to this point is the
proper allowance for time and/or
process to thoroughly dry these
materials. In defense of the new
U.S. EPA regulations, we must
acknowledge the fact that such
time and treatment prior to application
are the exception in the
fast-paced manufacture-to-market
cycle now in place in the U.S.
Beginning with materials produced
in January 2004, the EPA
has banned CCA for residential
use, whereas for some commercial
use it still is permitted. The practical
problem is that pressure
treaters serve large markets and
gain certain economies of scale by
producing only a single more
broadly accepted treatment type.
Since CCA is not acceptable for all
applications, it is simply more
cost effective for producers to tool
their manufacturing facilities for
the exclusive production of the
new, broadly permissible ACQ
type material.
There are several trade substitutes
for CCA. The most common
are:
• ACQ – Alkaline Copper
Quartenary (or as a shortcut,
simply Quat)
• CA or CBA (-A), CA-B –
Copper (Boron) Azole
• SBX – Sodium Borate (not
recommended for all applications)
The compositions of these new
preservatives are roughly as follows:
• ACQ solution: 49% copper
oxide, 33% quaternary ammonium
• Copper Azole (CBA-A): 49%
copper oxide, 49% boric
Acid, 2% tebuconazol
There are various qualities of
ACQ in the market; nevertheless,
the copper content in both ACQ
and CA is substantially higher
than in CCA. Conclusions based
on simplified theoretical corrosion
analysis and tests indicate that
fasteners corrode more rapidly in
lumber treated with the new CCA
substitutes.
Fastener Corrosion in ACQ and Other
“Next Generation” Treated Lumber
Martini and Wieland – 110
Primarily as a result of the
higher copper content, these new
wood preservatives are more
expensive than older CCA. This
means that beside the technical
problem of corrosion, there is a
potential economic problem.
Treated lumber is likely to become
more expensive than it was prior
to 2004, resulting in a longer
return of investment period. This
could have the effect of necessitating
that the fasteners perform
with intended values for a longer
time than before, despite the
increased corrosion risk. This
concept should add to the immediacy
and concern for this problem.
For purposes of this discussion,
we refer to these “next generation”
pressure treatments simply
as “ACQ,” as has become the
industry terminology, even
though CA is also a widely used
material.
UNDERSTANDING
CORROSION
Regardless of how corrosion is
defined – galvanic, atmospheric,
erosion, intergranular stress corrosion
– there is one thing that is
certain. Corrosion is a bad thing.
It must be staved off or delayed
using all available knowledge and
methods. This is only possible
when a scientific approach is
taken to the corrosion issues at
play in a given situation. Appropriate
remedies must be applied
to a problem. To do this, an
understanding of the corrosive
nature of the ACQ-treated lumber
as well as the materials or coatings
available for use in fastening
requirements is necessary.
There are several practical
questions that must be understood
in order to apply some certainty
to a material or coating
solution.
1. What level of corrosion tolerance
does the application
call for? Is a fastener effectively
corroded if surface
rust occurs, or the substrate
or exposed surface is
stained?
2. What is the application
environment to which the
coupling of lumber and fasteners
will be exposed? Will
it be closed, sheltered or
exposed to clean air, salt
spray, coastal, industrial,
hazardous, or acidic conditions?
3. What type and concentration
of preservative will be
in use?
The approach to a solution for
this complex fastener corrosion
problem is critical. Seeking the
lowest cost solution while trying
to cover each of the parameters at
play can lead to minor misjudgments
that in fact result in total
system failure. Because of the
clear need to combat all of the
potential corrosion concerns in
these materials, an appearance of
“overkill” may be necessary.
Material specifiers should keep
this in mind when confronted
with information from fastener
producers claiming effectiveness
against one particular aspect of
ACQ-related corrosion.
As clearly stated above, corrosion
is a very complex problem;
the above-cited parameters are
still only part of the puzzle. When
seeking answers to specific potentially
corrosive application questions,
it is common to receive a
simple answer like: “Understanding
the galvanic scale will tell you
if you have a potential problem.
Simply seek materials that are
electrochemically similar, and you
won’t have any problem.” But be
very careful. This simple approach
is very basic and while
true under certain circumstances,
it is impossible with limited information
such as knowledge of
materials specified for a particular
project, to make this claim. The
results, depending on other conditions,
can be completely the
opposite of what is anticipated. In
fact, with such limited information,
a specifier might as well simply
select the lowest cost materials
and hope for the best.
So what is the galvanic scale,
and what is it useful for?
All metal materials have a specific
electrochemical potential.
This potential is generally thought
of in the material’s most basic
application, such as pure water
from clean rain, absent acid rain
or salt spray. But most people
using these materials don’t truly
understand how significantly
these potentials can change
under very real, everyday conditions.
The electrochemical potential
of the metals listed in the adjacent
table is measured in a cell that
consists of the metal strip submerged
into a solution containing
its dissolved ions and a platinum
electrode submerged in an aqueous
solution containing hydrogen
ions. Voltage is measured between
these two elements. This sounds
very theoretical – and it is. Such a
standard scale is limited to pure
metals. It excludes metal alloys.
Pure metals are very rarely used
in construction applications. For
more practical use, potential is
measured in the same predefined
aqueous solution for all metals,
alloys included.
Among these three solutions,
not only are the potentials very
different, but the sequence too.
Look for example at steel versus
zinc. In the pH 6.0 water series in
the left column, zinc has a much
lower potential than steel. In the
pH 7.5 seawater series, the opposite
is true. This is the reason that
you will not find hot-dipped, galvanized
components on oceangoing
vessels. Therefore, if you are
confronted with a suggested corMartini
and Wieland – 111
rosion application solution using
only the potential scales, ask your
supplier in what aqueous solution
the scale was established. In the
case of ACQ, if the proposed corrosion
resistance approach is
measured in an ACQ solution
with a limited predefined concentration,
it may help to learn about
the interaction between copper
and a stainless steel part. But you
will still not be able to determine
the expected effect on a zinc-coated
carbon steel fastener in an
ACQ-treated piece of lumber.
Readers may have also
noticed in the table that in the
standard potential scale, steel is
missing. This is because steel is
actually an alloy of iron and carbon.
Alloys are not part of the
standard potential scale. But
nearly all metallic parts in contact
with treated lumber are alloys.
Even the more elaborate
graph adjacent, showing the corrosion
potential in flowing seawater
at 10 to 27°C (50 to 80°F) in
volts vs. standard hydrogen (upper
scale), saturated Cu/CuSO4
(middle scale) and saturated
Calomel [Hg/HgCl (lower scale)],
is of little help, because most lumber
is probably not intended to be
used in flowing seawater.
This elemental chart may,
however, be of some value to corrosion
specialists in that the very
low potential of Ni-Cr-Mo steel
may be of some interest.
Austenitic stainless steels such as
types 304 and 316 are Ni-Cr-Mo
steels.
In reality, one hardly has an
anode – cathode situation when
connecting treated lumber with
fasteners as the situation in
which the values above are measured.
An anode – cathode situation
means that a metal with a
higher electrochemical potential
and one with a lower electrochemical
potential are electrically connected
by an aqueous solution. In
the above example, the seawater
Practical
electrochemical
Series in water pH 6.0
Electrochemical series
for theoretical
elements ( standard
potentials)
Practical electrochemical
series in sea water pH 7.5
Metal E° mV Metal E° mV Metal E° mV
Silver 195 Silver 799 Silver 149
Copper 140 Copper 345 Nickel 46
Nickel 118 Lead -130 Copper 10
Aluminum -169 Tin -140 Lead -259
Tin -175 Nickel -230 Zinc (Zn 8 .5) -284
Lead -283 Cadmium 400 Steel -335
Steel -350 Iron 440 Cadmium -519
Cadmium -574 Zinc (Zn 8.5) -760 Aluminum -667
Zinc (Zn 8.5) -823 Aluminum –
1660 Tin -809
Potentials compared to a st andard hydrogen electro de
E°mV = Electrochemical potential in millivolts
Martini and Wieland – 112
was the aqueous solution. In a
typical anode – cathode situation,
the anode (low electrochemical
potential – e.g., zinc) dissolves
and the cathode (high electrochemical
potential – e.g., copper)
grows in mass as it is plated with
the dissolved metallic ions in the
aqueous solution. This principle
is precisely the method used to
intentionally electrically deposit
metals such as chromium or zinc
on steel components (plating). In
practice, this phenomenon is also
dependent upon the surface ratio
of the two electrodes, the conductibility
of the aqueous solution,
and the external contact of
the electrodes.
Often, there is substantial
real-world variation from the theoretical
expected corrosion of metals.
This is due to the dramatic
variability of environmental conditions
as described above. As a
result, we must rely on simulation
tests to approximate the true, reasonable
expected behavior of fasteners
in ACQ-treated lumber. Yet
there is a serious problem with
corrosion tests as well. Realistic
tests may take years for results to
appear, and accelerated tests lack
standardization.
One might suggest that if tests
take years for corrosion to appear,
then this is in effect a good sign
for the material being tested. This
is very far from the truth. In fact,
the only truly perfect test for simulated
corrosion testing is an
exact replica of materials being
tested under the exact application
environment, for the full expected
life of a connection. This means
that a 20-year roof would have to
be simulated for twenty full years.
Reasonable shorter cycle comparisons
may be made, but the
nature of corrosion of protection
coated materials (such as zincplated
or epoxy e-coated) is that
though the period prior to surface
breech may be extended, the
effect of the corrosive compound
on the eventually unprotected
steel may be dramatic and
extremely rapid. Accelerated tests
such as salt spray will produce
interesting results if a project is
planned for a coastal area or
northern urban area where road
salt is commonly applied.
But how would this compare
with test results of a non-cyclic,
high humidity test in a Kesternich
cabinet? The latter test would
make sense in an industrialized
zone. Unfortunately, there is a
temptation to use one or the other
test method for a special brand of
fastener or surface coat that gives
the most advantageous results
compared with those of a competitor.
Still, such non-cyclic humidity
test results, as shown below,
may give some indications about
the probable behavior of zinccoated
fasteners in wood treated
with the different preservatives.
But one should be aware that zinc
coatings vary in type and technique
of manufacture.
The chart of tested wood
material reflects the results of
actual tests performed at SFS
Intec labs in Heerbrugg, Switzerland.
It shows the corrosive
rates of zinc-plated fasteners in
lumber with the listed treatment
types, relative to the base process
– untreated pine lumber.
Nevertheless, results of a comprehensive
series of tests of noncyclic,
high humidity Kesternich
tests do allow for a better understanding
of what happens to fasteners
in ACQ-treated timber.
First, the test series proves
that, in general, corrosion of metallic
parts in ACQ-treated lumber
is stronger than in CCA-treated
timber. This is a key point. Regardless
of what else we are able
to determine, and absent any
long-term real-life experience, we
should be immediately alarmed
by this fact. Most specifiers would
be hesitant to make assurances
about life expectation for a product
known to be of lesser corrosion
resistance, with nothing
more definitive to establish an
opinion.
Second, all types of zinc-plated
fasteners begin corroding by producing
white rust – a popular
name for zinc oxide. Therefore,
zinc does not simply dissolve, but
oxidizes. At about the same rate,
stainless steel fasteners – 300 and
400 series – become copper plated
while carbon steel-based fasteners
begin to corrode. This means
that the copper in ACQ, which is
in the form of copper oxide, gets
reduced to pure copper and plates
the stainless steel fastener, which
acts as a cathode. This has no
adverse effect on the corrosion
resistance of the stainless materiMartini
and Wieland – 113
al. At the same time, however, the
zinc coating on the carbon steel
fastener oxidizes and no longer
provides the necessary protective
layer for the steel. The theoretical
effect is that the carbon steel
begins to corrode, producing red
rust or iron oxides. This is precisely
what is observed in lab
tests. Needless to say, no copper
plating occurs on the stainless
steel in untreated lumber and in
only minimal copper plating
occurs on the stainless in CCAtreated
lumber.
The tests, therefore, help us to
better understand what happens
in treated lumber. The process is
not the same as with screws in
metal structures. Here, the main
corrosion effect is not of galvanic
type but of oxygen type, also
known as general corrosion. The
galvanic mechanism occurs to a
smaller extent, depending upon
the materials being used.
From this we can draw several
conclusions. First, standard zinc
coatings are of little use. Thick
zinc coats, such as heavy hot dip
galvanizing, may help for a limited
time. Epoxy barrier coatings such
as commonly used roofing screw
e-coat (electromagnetic coatings)
will have the same minimal effect.
Other improved zinc coats may
also show a slowed corrosion rate,
but zinc oxide corrosion seems to
be unavoidable and with it the
fast degradation of
zinc. Zinc layers
exposed to the humidity
of the atmosphere
will corrode as well,
but the corrosion product
is a zinc carbonate
(due to the carbon
dioxide in the air) – a
strong, non-abrasive
protective layer that
slows corrosion to a
large extent. Zinc
oxide, or white rust,
has no such effect.
Again, tests support
this theoretical expectation.
Fasteners that were unscrewed
for periodic inspection exhibited
much more rapid corrosion than
fasteners left in place. The zinc
oxide was abraded and lost.
Although it offered only a minimal
protection function, its degradation
resulted in accelerated fastener
corrosion. While this oxide
removal process accelerates corrosion,
it does not promote it, and
therefore we can accept the observations
of these fasteners as a
prediction of the inevitable increased
corrosion of the undisturbed
test fasteners.
The conclusion is that austenitic
(300 series) stainless steel
fasteners should be used, as they
are virtually unaffected by the
wood preservative. If they are
plated with a thin zinc layer, it will
only serve to provide lubricity for
installation rather than to improve
corrosion resistance. After
installation, the zinc has no function
and may corrode away, leaving
the austenitic stainless steel
to fend off the corrosive effects of
ACQ on its own, which it will do
quite effectively.
Martensitic (400 series)
Stainless Steel
There remains a question.
Does martensitic stainless steel
(such as type 410) not perform as
well against ACQ? In terms of true
surface corrosion, neither martensitic
series 400 nor austenitic
series 300 (304 and 316) fasteners
showed visible degradation in
industry ACQ tests. But the 400
series (martensitic) fasteners produced
some stain on the surface.
This is to be expected and will
naturally be a problem where fastener
heads are visible on the
structure surface. Staining may
produce clearly visible spots that
dissipate into the lumber, leaving
the appearance that something is
wrong with the fastener.
Beyond cosmetic concerns,
400 Series martensitic stainless
steel fasteners are thermally hardened
and are more brittle than
300 Series austenitic stainless
steel fasteners. 400 series stainless
steels such as type 410 use
elevated carbon levels to achieve
hardenability. This is at the sacrifice
of corrosion resistance properties.
Further, there is significant
evidence that 400 series stainless
steels are susceptible to an altogether
different type of corrosion –
the phenomenon of stress corrosion.
While this is an entire subject
of its own, put simply, depending
on the environment in which
they are used, these materials
may develop intergranular corrosion
while under load, ultimately
leading to fastener failure. Therefore,
for purposes of this paper,
we only consider austenitic varieties
(300 series) as a viable consideration
as a solution to the
ACQ question.
RECOMMENDATIONS
We have noted that ACQ- or
CA-treated wood may be more
expensive than the traditional
CCA-treated lumber. Logically,
the payback period is longer and
the service life of fasteners may be
expected to be longer. For zinccoated
carbon steel fasteners, the
opposite applies. They corrode
faster in ACQ- or CA-treated
wood. The already existing disparity
between the expected service
Standard Zn-plated carbon steel fastener
after 154 hours in ACQ lumber chamber.
Martini and Wieland – 114
lives of lumber and carbon steel
fasteners increases – not in favor
of the fasteners.
To gain a service life equilibrium
between ACQ- or CA-treated
lumber and the fasteners used to
join it, it is strongly and exclusively
recommended that austenitic
(300 series) stainless steel fasteners
be used. This will also
serve to eliminate the ugly staining
on the lumber or other material
surface. Even such fasteners
with a carbon steel tip for improved
installation will be effective,
provided that adequate fastener
length is specified to ensure
that the integrity of the fastener
remains long after the carbon
steel tip is corroded away.
Under an industry test, fasteners
were left for 154 days in a
Kesternich cabinet with pure
water humidity at a temperature
around 104°F degrees. The two
adjacent images show carbon
steel and austenitic stainless steel
fasteners after the simulation.
Whereas the carbon steel fasteners
were heavily corroded to a
condition where structural safety
would be compromised, the
austenitic stainless steel series
300 fasteners showed very little
corrosion. The head of the stainless
fastener exhibited some white
rust caused by the zinc coat that
is applied for installation lubricity,
and the carbon steel tip exhibited
some stain and red rust. This
tip is designed and expected to fail
over time and the head and shank
are protected, as they are comprised
of stainless steel under the
thin zinc coating. Corrosion,
therefore, is limited to zones
where it produces no harm.
CONCLUSION
ACQ/CA pressure treatments
are proven to be more corrosive
than traditional CCA wood treatments.
Galvanic as well as oxygen-
related corrosion occurs in
these materials. Because of the
variable environments in application
as well as the condition of
wood material at delivery (moisture
content variability), corrosion
prevention cannot be accomplished
through improved workmanship
or care. Further, due to
high variability in materials and
conditions, existing coatings such
as zinc and epoxy e-coats are likely
to be of little long-term effect in
reliably preventing this corrosion.
Certainty can only be gained
through the use of austenitic
stainless steels for fastening these
materials.
Austenitic stainless steel fasteners
are more costly than coated
carbon or martensitic stainless
steel fasteners. This cost difference,
however, pales in comparison
to the potential catastrophic
costs of roof, panel, trim, or other
structural failure due to misapplied
carbon steel fasteners in
ACQ- or CA-pressure treated lumber
materials. Specifiers must be
cautious and mindful of available
industry information that is clearly
designed to support proprietary
products and treatments. Extensive
studies and data must be
insisted upon. As discussed herein,
there are no simple answers to
complex corrosion issues such as
ACQ.
Zinc plate carbon steel 304 stainless steel with
carbon tip
Fasteners after 154 days in non-cyclic Kesternich high humidity
chamber, with periodic removal for inspection: