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Osmosis and the Blistering of Polyurethane Waterproofing Membranes

May 15, 2010

ABSTRACT
Cold-applied, asphalt-modified, elastomeric
polyurethane waterproofing membranes
(polyurethane membranes) have
been popular for roofing and waterproofing
applications in the Pacific Northwest and
British Columbia for at least the past 15
years. Relative low cost and easy application
resulted in their widespread use in
inverted roofing and waterproofing membrane
assemblies (IRMA) applied to concrete
decks. However, water-filled blisters under
these membranes have been discovered on
numerous buildings in the Pacific
Northwest in recent years. In some cases,
the blisters were so large that replacement
of the membrane was required. Water leakage
to the interior can result when the blister
expands to a crack or joint in the concrete
slab.
The local building science and roofing
industry is aware of the problem but lacks
a complete understanding of causal effect
or of the physics of moisture transfer. Water
vapor diffusion and capillary flow do not
adequately explain the pressures or volumes
of water contained within these discrete
water blisters. Moisture transfer via
osmosis can result in blisters under significant
pressure and potentially explains the
observed conditions. Osmosis is the physical
transfer of water through a semipermeable
membrane when separating solutions
of different dissolved ion (salt) concentrations.
Under osmotic pressures, water will
flow through a membrane from the less
salty side to the more salty side, in order to
reach equilibrium.
A series of laboratory experiments was
performed to demonstrate that the required
conditions for osmosis to occur exist in the
field. Laboratory testing of several of these
membranes confirmed they are semipermeable
to water (in order of 60 to 420
ng/Pa·s·m2 for typical thicknesses). Re –
searchers also confirmed a significant dissolved-
salt-ion concentration in the water
collected in the field from beneath the membranes.
Finally, osmotic flow was measured
through several of the membranes using a
controlled laboratory apparatus. The measured
flow through these membranes in the
laboratory is in the correct order of magnitude
to explain the large water-filled blisters
and pressures observed in the field.
This article demonstrates osmotic flow
through polyurethane membranes and
attempts to create an industry awareness of
the issue. Ongoing research is under way to
refine polyurethane waterproofing membranes
to reduce their susceptibility to
osmosis and prevent future occurrences of
water-filled membrane blistering.
INTRODUCTION
Over the past several years, RDH Build –
ing Engineering, Ltd. has reviewed dozens
of asphalt-modified polyurethane membrane
applications ranging from five to 15
years of age. The membranes are applied to
sloped concrete slabs in both insulated and
uninsulated inverted roof and waterproofing
membrane assemblies (IRMAs). Typically,
water-filled blisters have formed between
the membrane and the concrete deck and
are often under considerable pressure.
These self-contained, pressurized water
blisters have no identifiable leakage path
through or around the membrane. Blisters
range in size from a penny to entire roof
deck areas and can contain significant
quantities of water. In some cases, large
blisters (>50 mm deep) have displaced concrete
pavers, creating hazardous walking
conditions. As blisters expand over cracks
or joints in the concrete, water can leak to
the interior.
In the Pacific Northwest, the blisters
described above have been observed with
asphalt-modified polyurethane membranes
used in IRMA construction and not in other
conventional roofing systems such as hot
rubberized asphalt or sheet-applied SBS
modified bitumen. In an IRMA, the membrane
is installed directly on the structural
concrete beneath insulation (if separating
heat space) and ballast or wear course. In
the wet Pacific Northwest climate, moisture
remains in contact with the membrane for
much of the year.
Hygrothermal analysis shows that vapor
diffusion can transport water through
polyurethane membranes due to their relatively
high vapor permeance compared to
other roofing and waterproofing membranes
(>1 U.S. perm vs. <0.01 perm). However, the
quantity of water transported by vapor dif-
DE C E M B E R 2010 I N T E R FA C E • 1 5
This article is reprinted from the Proceedings of the RCI Building Envelope Technology Symposium, held Oct. 26-27, 2009, in San Diego, CA.
fusion is not of the magnitude
required to ex –
plain the blistering, nor
are water vapor pressures
sufficient to ex –
plain the high hydrostatic
pressures that exist
within the blisters.
To explain the large
volumes of water and
high pressures within
the blisters, we hypothesize
that osmosis is acting
to transport water
through the membrane. In the roofing
industry, the concept of water flow by osmosis
is uncommon. The process of osmotic
flow has been reported to cause failure of
flooring and traffic membranes and is a
consideration in the design of bridge decks
and water tanks where exposed to groundwater,
saltwater, or road de-icing salts. It is
also a reported problem and design consideration
with glass fiber-reinforced boat
hulls, where osmosis can
form blisters within the
fiberglass.
Objectives
The objectives of this research study are
as follows:
• Confirm that osmotic flow is a significant
contributor to the observed
in-situ blistering of polyurethane
membranes directly applied to concrete
in IRMA construction.
• Develop a test method to determine
the susceptibility of a membrane to
osmotic flow, and measure the rate
of osmotic flow under various salt
concentrations.
• Determine a possible relationship
between water vapor permeance and
osmotic flow.
• Create awareness and highlight the
need of osmosis control for the
inclusion in current Canadian and
U.S. standards for liquid-applied
waterproofing membranes.
Background
Asphalt-modified polyurethane membranes
have been used in hundreds of buildings
constructed over the past 15 years in
the Pacific Northwest and Lower Main land
of British Columbia. Their relatively low
cost and easy application have led to widespread
use in IRMA construction, both
insulated and uninsulated, as well as for
planters, fountains, and foundation walls.
RDH and other local consultants have
reviewed dozens of buildings in which the
polyurethane membranes have blistered.
Blisters are also a frequent occurrence in
fluid-applied polyurethane membranes in
Japan (Tanaka et al. 2007 and 2008).
Water-filled blisters range from penny sized
Figures 1 and 2 –
Typical blistered roof
membranes. Blisters
range from penny sized
to areas several square
feet in a 5- to 10-yearold
membrane.
Figure 4 – Water beneath blistered
membrane over entire deck.
16 • I N T E R FA C E DE C E M B E R 2010
Figure 3 – Large “waterbed”-type blister lifting pavers.
3”
32”
to those that encompass entire decks
(Figures 1 and 2). Unlike vapor blisters filled
with air and caused by other mechanisms,
these are filled with water under considerable
pressure. Larger blisters can lift ballast
and pavers, creating a hazardous “wa –
terbed” effect when one walks on the surface
(Figures 3 and 4). Small blisters typically
do not result in direct leaks to the interior;
however, larger blisters that encompass
a crack or joint in the concrete tend to
manifest into leaks to the interior.
Investigating IRMA construction is challenging
because ballast and insulation need
to be removed to expose the membrane. As
a result, only small, random areas of the
membrane are typically reviewed. Larger
areas of membrane typically get exposed
only when leaks are reported, when blisters
have become so large that they lift up the
ballast or pavers, or when the membrane is
replaced.
Blisters typically occur on horizontal
surfaces, but they have also been observed
on vertical surfaces of water features,
planters, and green roofs. In IRMA construction
located in the Pacific Northwest, it
is not uncommon for water to remain at the
membrane surface year round. When
inverted roofing and waterproofing are
investigated in the summer, even after
many weeks of dry weather, water exists at
the membrane surface, held by capillary
forces between the membrane and insulation/
drainage mat layer and prevented from
evaporating by the dimpled polyethylene
drain mat or insulation installed above.
In RDH’s experience, the following factors
appear to increase the severity and size
of the blisters:
• Blisters are often more severe at low
points and at areas of poor slope,
i.e., ponding. However, blisters still
do occur where the slab is well
sloped to drains.
• Blisters are typically larger and
more prevalent at areas where the
membrane is thinner.
• The size or severity of the blisters
does not appear to be affected by the
use of either drainage mat or
extruded polystyrene insulation
applied directly over the membrane.
• Blisters are almost always larger
and more frequent in older membranes.
In review of available literature, the
authors found little information regarding
the blistering of polyurethane membranes
in IRMA construction, suggesting that the
mechanisms causing the failure are not well
understood by the roofing and waterproofing
industry.
MECHANISM OF MEMBRANE BLISTERING
Osmosis Process
Osmosis is a naturally occurring phenomenon,
wherein water (or other solvent)
flows through a semipermeable membrane
from a solution of low-salt (solute) concentration
(hypotonic) to a solution of high-salt
concentration (hypertonic), without the
input of energy (Oxtoby et al., 1999).
Osmosis can be countered by increasing
the pressure of the hypertonic solution with
respect to the hypotonic side. Osmotic pressure
is the pressure required to maintain
equilibrium between the two sides with no
net movement of solvent. Osmotic pressure
depends only on the molar concentration of
the solute, not the type of solute present.
Therefore, if any difference in solute is present
across a membrane, osmosis will
occur.
Essentially, if a semipermeable membrane
separates a tank of fresh water and
saltwater, the fresh water will flow through
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DE C E M B E R 2010 I N T E R FA C E • 1 7
the membrane to the salty side until equilibrium
(equal concentration) is achieved. If
left unrestrained, fresh water would essentially
fill up the salty side until the water
head pressure was equal to the osmotic
pressure. The semipermeable membrane
must be permeable to the solvent (i.e.,
water) but not to the majority of solutes
(salt, metal, and contaminant ions); otherwise,
equilibrium will be achieved by dissolution
through the membrane. Depending
on the molecular structure and pore size of
the membrane, certain salt ions may pass
through freely while other larger and heavier
metal ions may not. In this case, osmosis
will still occur.
Reverse osmosis used in water filtration
systems essentially applies a high water
pressure (>50 psi) to counteract the osmotic
pressure and force water ions through a
specially developed semipermeable membrane
to create fresh water. Reverse osmosis
membranes have been developed with
these properties in mind, to allow only H2O
ions to pass through, rejecting other, larger
salt ions, which provides greater than 99%
effectiveness. The processes of osmosis and
reverse osmosis are demonstrated in Figure
5.
The two laws governing the osmotic
pressure of a dilute solution were discovered
by the German botanist W.F.P. Pfeffer
and the Dutch chemist J.H. van ’t Hoff
(Oxtoby et al., 1999). The laws state that the
osmotic pressure of a dilute solution at a
constant temperature is directly proportional
to its concentration and that the osmotic
pressure of a solution is directly proportional
to its absolute temperature. Osmotic
pressure is analogous to Boyle’s law and
Charles’s Law for gases. The ideal gas law,
PV = nRT, has an analog for ideal solutions
in the form of πV = nRTi. This is rearranged
in Equation 1 in terms of molar concentration
and solving for osmotic pressure, π.
Equation 1
Where: π = osmotic pressure; i = the
number of ions produced during dissociation
of the solute; M = the molar concentration
of all solutes, moles/L; R = 8.3145
J/K·mol (0.083145 L·bar/moles·K), the
molar gas constant; and T is absolute temperature,
Kelvin.
In solutions containing multiple types of
dissolved salts, the partial osmotic pressure
for each is added to determine the overall
osmotic pressure across the membrane.
Essentially, it is the difference in total dissolved
solids (TDS) that causes the pressure.
Reverse osmosis membrane manufacturers
have simplified this formula to the
following in terms of pressure in psi to sizereverse
osmosis filtration systems
(Lenntech 2008):
Equation 2
Where: Σmj = the sum of molality concentration
of all constituents in a solution
(moles of solute/kg of solvent), and T is the
absolute temperature in Kelvin.
For example, saltwater from the ocean
will have a total dissolved solids concentration
of approximately 36,000 mg/L or ppm
(Lenntech, 2008). This concentration has a
total osmotic pressure difference of almost
26 bar (2.6 MPa) at 20°C (68°F). Brackish
water (i.e., well water contaminated with
ground salts) may have a total dissolved
solids concentration of 500 mg/L, which
results in a pressure of 0.25 bar (25 kPa) at
20°C (68°F). These osmosis pressures give
an indication of the pressure required in a
reverse osmosis filtration system.
Figure 5 – Osmosis, equilibrium, and reverse-osmosis flow through a membrane.
18 • I N T E R FA C E DE C E M B E R 2010
Blistering Process
We hypothesize that the formation of a
blister occurs in two stages. In stage 1, a
film of liquid water forms at the concrete-tomembrane
interface, likely at a surface void
in the concrete beneath the membrane.
Various sources can form the initial film of
water, including vapor diffusion and capillary
flow downward through the
polyurethane waterproofing membrane or
water initially in the concrete slab from construction
or rainwater. Once a film of water
forms, vapor pressures on both sides of the
membrane are equal and vapor diffusion
ceases. In stage 2, the water film dissolves
minerals from the concrete, increasing the
salinity. Once this osmotic cell starts,
osmotic pressures draw water through the
membrane, creating water-filled blisters. As
the pressure in the blister increases, it
debonds from the concrete at the perimeter,
enlarging the blister and allowing the
process to continue and the blister to grow
in size over time.
A typical IRMA is depicted in Figure 6.
Rainwater flows down through the ballast,
insulation, and drainage layers to the
waterproofing membrane. Throughout the
wetting process, water is adsorbed on the
surfaces and into the pores of the materials
within the assembly, remaining there even
after the bulk of the rainwater is drained
away. This creates a layer of water and
vapor at 100% RH at the membrane surface.
Extruded polystyrene has a vapor permeance
of approximately 15 ng/Pa·s·m2
(per 100 mm); and drainage mat, made of
dimpled, high-density polyethylene, has a
vapor permeance of less than 1 ng/Pa·s·m2.
The ability of an IRMA to dry upward by
vapor diffusion through these materials is
limited. The concrete also has a relatively
low vapor permeance, with a wet permeability
estimated from 0.5 to 5 ng/s·m·Pa
(WUFI, 2009; ASHRAE, 2005; Onmura et
al., 2009). Thus, a 150-mm-thick slab has a
vapor permeance ranging from 3 to 30
ng/Pa·s·m2. Interior ceiling finishes or coatings
will reduce this further. The vapor
pressure differences during wet periods of
the year are shown graphically in Figure 7.
Even during the warmer summer
months and under solar heating, the insulation
above the membrane maintains the
concrete temperature relatively constant,
and, as a result, minimal heat is provided to
dry out the excess or absorbed water. Field
experience and hygrothermal modeling
show that even when bulk surface water
dries out, the relative humidity above the
membrane re mains above 90% year round,
maintaining a constant
vapor pressure
drive from
the exterior to the
interior. Therefore,
whether liquid wa –
ter or water vapor
is present at the
roof membrane
sur face, there will
be an almost constant
vapor pressure
drive in –
wards, which will
effectively prevent
significant drying
from occurring up –
wards through the
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Figure 7 – Vapor drive from saturated roof membrane interface to the
interior and exterior.
DE C E M B E R 2010 I N T E R FA C E • 1 9
Figure 6 – Typical IRMA waterproofed with a polyurethane membrane.
membrane. As a result, indoor humidity
and temperature do not have a significant
effect on the degree or severity of blistering.
This is supported by the authors’ field
observations of blistered membranes over
all types of occupied and unoccupied
spaces, including occupied residential
suites, mechanical rooms, pools, parking
garages, and exterior spaces.
Figure 8 depicts the concrete moisture
content output from a seven-year WUFI 4.1
hygrothermal simulation of the inverted
roof assembly discussed above, with two
different levels of membrane vapor permeance.
The plot compares a 30-mil
polyurethane membrane (vapor permeance
= 400 ng/Pa·s·m2) and a two-ply SBS membrane
(vapor permeance < 1 ng/Pa·s·m2).
WUFI does not account for moisture flow by
osmosis, but it does model vapor and capillary
transport through the membrane and
concrete. The impact of rainwater wetting
and sitting on the membrane between rain
events was accounted for in the model;
however, the waterproofing membrane was
assumed to have no capillary suction, consistent
with other membrane material properties
listed in the WUFI database.
The simulation demonstrates that the
polyurethane membrane will allow a net
wetting of the concrete from vapor diffusion.
During a typical year, more moisture is
transported through the membrane into the
concrete than can dry out of the concrete
itself. This analysis is sufficient to show
that over time the concrete under the membrane
will become saturated. However, once
the top surface of the concrete becomes saturated,
the vapor pressure will be equal on
both sides of the membrane, diffusion will
stop, and there will be no driving pressure
to create a blister.
Once the concrete is wet, salt ions in the
concrete aggregate, cement, and admixtures
dissolve into available water at the
surface. This dissolution of ions from the
concrete creates the required salt concentration
difference between the top and bottom
of the membrane for osmosis to begin.
Once started, osmosis continues until the
salt concentration gradient is removed or
water is removed from the freshwater side of
the membrane. The process is slow to start
but accelerates rapidly once small quantities
of liquid water are present beneath the
membrane. The osmosis mechanism is
summarized in Figure 9.
HYPOTHESIS OF OSMOTIC FLOW
For osmotic flow to occur across a membrane,
two requirements must be satisfied:
1. The membrane must be semipermeable
to water molecules and not salt
molecules, and
2. Liquid water of different salt concentrations
must be present on both
sides of the membrane.
To prove the hy –
pothesis that osmotic
flow can occur
across polyurethane
membranes, samples
of membrane
and water from the
blisters were collected
from several
build ings. The water
vapor permeability
of the blistered
mem branes was
mea sured and the
sampled water analyzed
to determine
the salt ion concen-
Figure 8 – Modeled moisture content of concrete slab with SBS and polyurethane waterproofing.
Figure 9 – Blister formation mechanism by osmosis.
20 • I N T E R FA C E DE C E M B E R 2010
tration of both the blister water and the
water collected from the top surface of the
membrane.
Water Vapor Permeance Testing of
Polyurethane Roof Membranes
Water vapor permeance of the sampled
polyurethane membranes was measured
under dry-cup, wet-cup, and inverted-wetcup
conditions in general conformance with
ASTM E96. Vapor permeance of new
polyurethane membrane samples provided
by several manufacturers and control samples
of other waterproofing membranes
were also measured for comparison. Vapor
permeance test results correlated with published
and unpublished data provided by
the membrane manufacturers.
Measured water vapor dry-, wet- and
inverted-wet-cup permeance data for three
different polyurethane membranes are provided
in Figure 10. Results for three lowpermeance
roofing membranes are also
shown for comparison purposes. Invertedwet-
cup testing (wet-cup sample inverted so
that liquid water is in direct contact with
sample) is not always performed by most
roofing membrane manufacturers but provides
the best indication of vapor permeance
under realistic exposure conditions for
a membrane in an IRMA system.
Two of the results are for aged
polyurethane membrane samples removed
from their sites: Membrane 1 and 2, both
approximately ten years old. Membrane 3 is
a new sample of a similar polyurethane
membrane from the same manufacturer as
Membrane 1. The installed membrane
thick nesses of 30 and 60 mils for Mem –
branes 1 and 2 are considered thin by
today’s standards but were common in the
Vancouver market 5 to 15 years ago.
The results show that the polyurethane
membranes are relatively permeable compared
to other roofing and waterproofing
membranes, especially inverted-wet-cup
measurements. The relationship between
water vapor permeance and osmotic flow
through a membrane is not fully understood
at the microporous level; however, we
believe they are intrinsically related. If the
membrane has a measureable water vapor
transmission rate, then it makes sense that
it will have an “osmotic flow” transmission
rate as well. If the membrane pore structure
allows the passage of water ions but not all
dissolved salt and metal ions, then osmotic
pressures can be developed.
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DE C E M B E R 2010 I N T E R FA C E • 2 1
Water Absorption of Polyurethane
Membranes
Water uptake testing of the poly ure –
thane membrane samples was performed to
determine if water absorption is related to
osmotic flow. If a material will absorb water
into its pore structure, it follows that water
may also be able to flow through it.
Membrane samples were submerged in
water for over three months and weighed
periodically until the mass remained constant
for longer than two weeks. Both aged
membrane samples absorbed approximately
16% to 17% moisture content by mass,
and the new membrane sample absorbed
approximately 4%. Moisture absorption in
all samples generally stopped after two to
three weeks. The higher absorption in the
aged samples may be due to the poly ure –
thane filler materials and reinforcing mesh
fabric used by both manufacturers at the
time. These water absorption tests appear
to indicate that water is able to pass through
the pore structure of these membranes.
Dissolved Salt Concentration of Blister
Water
Samples of water and membrane at
large blisters from two different buildings
were collected for laboratory testing. The
water was analyzed to confirm different salt
concentrations between samples collected
from above and below the membrane.
Samples of water were extracted from the
membrane blister with a syringe and small
hand pump and collected from above the
membrane (rainwater). Both samples were
sent to an independent laboratory for analysis
of dissolved metals concentration. At a
large blister in Membrane 1, approximately
12 in of hydrostatic water head (~3 kPa) was
measured prior to the extraction of the sample
water. The wa –
ter inside the blister
had a dark
brownish tint, similar
to all of the
blisters reviewed, and is likely to be the
result of continual contact with the bitumen
in the asphalt-modified polyurethane membrane.
See Figures 11 and 12.
A water-quality laboratory analysis
determined the dissolved solid concentration
for 30 of the most common dissolvedmetal
ions. Table 1 includes the results provided
by an independent water-testing laboratory
of the membrane blister water and
rainwater taken from one of the buildings
where Membrane 1 was used.
As suspected, the blister water had high
levels of several dissolved metal ions, the
majority of which were sodium and potassium
ions. The mix of dissolved metal ions at
the blister water is likely from minerals
within the aggregates, cement, admixtures,
and polyurethane membrane itself. Silicon,
present in cement (calcium silicates
CaO·SiO2), indicates dissolution from the
concrete. The level of dissolved ions within
the blister water was considerably higher
than rainwater, and for reference, is more
saline than brackish water but much less
than seawater.
Figures 11 and 12 – Cutting of membrane blister and
expulsion of water during extraction process.
Figure 10 – ASTM E96 – Vapor permeability and permeance laboratory results for membrane samples.
22 • I N T E R FA C E DE C E M B E R 2010
Initial calculations predict that an
osmotic pressure of approximately 326 kPa
was present at this blister. While this pressure
could not have been physically contained
within this elastic membrane, it is
better visualized as a pressure potential
that causes suction of liquid water through
the membrane. In reality, the pressure
within the blister is moderated by failure of
the membrane-to-concrete bond at the
sides of the blister and stretching of the
membrane under tensile stresses.
VERIFICATION OF OSMOTIC FLOW
Apparatus
To measure osmotic flow through the
membranes, an apparatus was developed
and tested. A piece of the polyurethane roof
membrane is used to separate
distilled and saltwater.
If osmosis flow occurs
across the membrane,
water will flow from the
distilled water reservoir
through the membrane
and into the saltwater
until equilibrium occurs
or the pressure developed
in the container is equal
to the osmotic pressure
(Oxtoby et al., 1999). By
measuring the mass and
volumetric change of the
container holding the saltwater
and membrane at regular intervals,
the osmotic flow can be measured.
Distilled water was used to represent
rainwater, and water removed from several
membrane blisters was used as the saltwater.
Polyurethane and other roofing membranes,
ranging in thickness from 30 to 150
mils, were tested, as was a commercial
reverse osmosis membrane, as a “proof-ofconcept”
exercise. Figure 13 demonstrates a
concept of the apparatus, and Figure 14
shows a schematic of the container and
photograph of one of the proof-of-concept
test specimens.
As a proof-of-concept experiment, a
commercial reverse osmosis water filter was
disassembled and a sample of the osmotic
membrane put into the apparatus with the
blister water removed from site. Other salt
solutions using common table salt were
also tested. Flow through the membrane
initially was in the order of 15 L/m2/day
before immense pressures developed in the
containers. This order of flow is comparable
to what is advertised by the osmosis membrane
in a water filtering application. As a
result of the high pressures developed, several
of the container lids burst during the
test procedure. In Figure 14, a total of 58
mL (25 L/m2) of water was transported
through the reverse osmosis membrane, as
was measured in the container at the end of
31 days.
Procedure
Samples of polyurethane membranes
discussed in the previous sections were
tested using the osmotic-flow test apparatus.
Samples of saltwater removed from the
blisters were used in conjunction with the
membrane samples to demonstrate osmotic
flow under the specific field conditions.
Initial testing focused on two of the aged
polyurethane membranes (1 and 2).
Samples of the membranes and saltwater
from the blisters were put into the test
apparatus and tested as follows:
1. Samples of membrane were cut to
precisely fit into the screw-top
“open-top” lid of the glass jar. Each
sample was initially weighed, and
the thickness was measured.
2. A known mass of saltwater was
placed into the glass jars.
3. Membrane samples were bedded
into waterproof epoxy within the lid
flange of the glass jar. Epoxy was
also used between the membrane
and the glass. The screw-top lid provided
compression and a watertight
fit of the membrane at the edges.
The membrane acted as a gasket;
Table 1 – Dissolved metals concentration – Building 1 (30-mil membrane sample).
Figure 13 – Osmotic flow testing apparatus schematic.
24 • I N T E R FA C E DE C E M B E R 2010
WATER FROM WATER FROM ABOVE
BENEATH MEMBRANE #1 MEMBRANE
(BLISTER WATER) (RAINWATER)
Soluble Metal Ions in Dissolved Solid Dissolved Solid
Solution Concentration, mg/L, ppm Concentration, mg/L, ppm
Sodium 2960 1.89
Potassium 574 0.47
Sulphate 75.3 <1.0 ppm
Magnesium 1.83 0.35
Phosphorous 1.82 <0.2 ppm
Silicon 29.9 <1.0 ppm
Calcium 3.4 4.0
Other dissolved metals Trace amounts of None present
several, <1ppm
Total dissolved solids ~3650 ppm ~7 ppm
Hardness, CaCO3 equivalent 16.0 11.5
how ever, waterproof
epoxy was
used to aid with
sealing the membrane
in place and
to seal the container.
4. After the epoxy had
cured and the container
was leak
tested, the initial
mass of the container,
membrane,
and saltwater to –
gether were measured.
5. Membrane coupons
(blank samples)
were produced,
measured, weighed, and submerged
in the freshwater bath. The water
level of the freshwater was kept
equal to that within the container to
eliminate the effect of hydrostatic
pressure head.
6. At regular intervals, the containers
and blank samples were removed
from the freshwater bath, dried
thoroughly, and weighed. This
process was repeated approximately
twice a week for several months. For
samples with significant osmotic
flow (i.e., through an osmosis membrane),
the volumetric increase can
also be measured using graduations
on the sample container.
7. The flow of water through the membrane
was measured by subtracting
the incremental mass from the initial
container, water, and sample
mass. The glass container, lid, and
epoxy did not absorb water (confirmed
by producing empty container
blanks and submerging them in
water), so any change in mass was
Figures 14 a (above) and b (right) – Osmotic flow testing con –
tainer schematic and photograph of increase in water volume.
Building Envelope
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DE C E M B E R 2010 I N T E R FA C E • 2 5
the result of absorption into the
membrane and flow into the salty
water within the container.
8. To isolate osmotic flow, the absorption
rates of the membrane samples
must be known. For the two membranes
tested, each gained approximately
17% moisture by mass within
three weeks and remained constant
for the remainder of the test.
Blank samples were used to determine
the required time and mass of
water for absorption to saturation to
occur. Following this initial uptake,
additional mass/volume gain of the
containers was by osmosis flow
through the membrane. This can
also be confirmed by measuring the
volume of water within the container
and the subsequent pressure
developed.
Results
Measured osmotic flow rates through
30- and 60-mil samples of Membranes 1
and 2 are presented in
Figure 15. Several
additional samples of
these membranes are
currently being tested
and show similar flow
rates.
Small deviations
result from precision of
weighing the samples
(to nearest ±0.01g of
container mass), but
otherwise a constant
flow rate was measured.
With this setup,
it appears to take a few
weeks for the membrane to become fully
saturated before osmotic flow rates can be
determined. On average, an osmotic flow
rate of between 8 and 13 g/m2/day was
measured.
As shown, both membrane samples
have similar order-of-magnitude osmoticflow
rates. Over time, the osmotic pressure
should decrease with a lower salt concentration;
however, the volume of water needed
to reach equilibrium is many times the
size of the jars. Thus, we wouldn’t expect to
see a significant change in slope on the
graph measuring osmotic flow in the 150-
day test period. However, as pressure develops
within the blisters in the field and the
membrane pore structure stretches and
opens up, the osmotic flow rate may be
affected. The blister water contains many
different salt ions at varying concentrations.
Over time, some of the low concentration
salts will reach their equilibrium pressure,
marginally reducing the flow rate.
Further experiments are ongoing to
determine the effects of the osmotic pressure
and osmotic
flow. Figure 16
shows initial results
for 0.1 and 1.0 molar
NaCl salt solutions
compared to distilled
water (blank sample)
and the blister water.
Comparing the
osmotic flow rates of
the three salt solutions
to the distilled
water confirms that
the salt concentration
has a direct
effect on the rate of
osmosis through the
polyurethane membrane.
The lack of
flow through the con trol distilled wa ter
sample also confirms that the process of
osmosis is pulling water through the membrane,
not capillary suction or another
mechanism.
Based on continued research under way
with new unaged polyurethane membranes
with and without various primer coatings,
preliminary osmotic flow rates of 0.5
g/m2/day to 7 g/m2/day have been measured
in the laboratory. The intent of this
further research is to reduce the osmotic
flow rate through new membranes to as
close to zero as possible to prevent blisters
from forming.
Discussion
The measured osmotic flow rate through
the aged polyurethane membranes (with the
saltwater removed from the blisters) is, on
average, between 8 and 13 g/m2/day. For a
membrane in an IRMA application continually
exposed to water, in one year, this flow
rate equates to between 3 and 5 L/m2 of
water (3 to 5 mm deep) transported by
Figure 16 – Comparison of osmotic flow through Membrane 1 with different osmotic suction pressures.
26 • I N T E R FA C E DE C E M B E R 2010
Figure 15 – Polyurethane Membranes 1 and 2 – measured osmotic flow through membrane.
osmo sis. In ten years, this is on the order of
30 to 50 L/m2 or water (30 to 50 mm deep),
which corresponds to the volume contained
beneath the membrane in blisters we have
observed at several buildings. Blisters are
often observed to be 3 mm to 25 mm tall,
and in extreme cases, where the pavers are
floated, greater than 50 mm.
Continuous exposure to liquid water
will affect blister formation, and it is likely
that some blisters may grow and shrink
seasonally when water is present on top of
the membrane. In addition, both membrane
adhesion and tensile strength of the membrane
will affect how large the blisters grow
in the field. Blisters will also stop growing if
the pressure becomes equal to the osmotic
suction pressure or if the blister does not
continue to grow by adhesion failure or
stretching, which may occur at low salt concentrations
and osmotic pressures.
In the IRMA application, wetting of the
concrete surface by osmosis is shown to be
up to an order of magnitude higher than the
drying capability of the assembly. Above the
membrane, RH remains high, between 90%
and 100% year round. As a result, drying
outward is slow through the insulation and
drainage mat: at the rate of less than 0.1
g/m2/day. On the bottom side, drying
through the concrete is also a very slow
process, and vapor flow inward through the
concrete is estimated to be on the order of 1
g/m2/day (dependent on concrete properties).
These mechanisms for drying are
slower than the wetting process, and moisture
accumulates beneath the membrane.
The osmotic cell develops immense suction
pressures that cause blisters to form and
expand, acting to delaminate and stretch
the membrane. As the process progresses,
the blisters expand into each other until
very large water-filled blisters develop.
CONCLUSIONS
Severe water-filled blistering of coldapplied,
asphalt-modified elastomeric poly –
urethane waterproofing membranes is a frequent
problem for inverted roof membrane
assemblies in the Pacific Northwest. RDH’s
testing and research demonstrate that the
water-filled blisters can be explained by the
fluid transfer mechanism of osmosis. The
research confirms that osmotic flow does
occur through these membranes, the conditions
for osmosis to occur exist in the field,
and our test results replicate the same
order of magnitude of moisture transfer
observed in the field.
The rate of osmotic flow is a function of
the vapor permeance of the membrane.
Therefore, lowering the vapor permeability
of the polyurethane membrane will likely
reduce the potential for osmosis to start by
decreasing the potential for the top surface
of the concrete to become saturated and will
likely result in a lower rate of flow under
osmotic pressures.
The aged polyurethane membranes that
were removed from blistered roofs and tested
were found to be semipermeable and
have a vapor permeance ranging from 60 to
420 ng/Pa·s·m2, depending on application
thickness and chemical composition. Some
new polyurethane membranes that have
also been tested have similar order-ofmagnitude
vapor permeance values (up to
120 ng/Pa·s·m2), even when tested with certain
concrete primers.
Osmotic flow rates measured through
aged polyurethane membranes that were
removed from blistered locations are on the
order of 8 to 13 g/m2/day. Preliminary testing
has also been performed on new primed
and unprimed polyurethane membranes
that are currently available on the market,
with measured flow rates of between 0.5 to
7 g/m2/day, depending on membrane
chemistry, thickness, and primer application.
These lower flow rates are still in
excess of most other waterproofing and
roofing membrane systems, and at this
time, it is not known if these flow rates are
low enough to prevent blisters from occurring
within the expected service life of the
membrane. Further research is needed to
develop an acceptable solution.
The two most relevant standards that
cover the manufacture and installation of
asphalt-modified polyurethane membranes
are ASTM C836-00, Standard Specification
for High-Solids-Content, Cold, Liquid-Applied
Elastomeric Waterproofing Membranes for
Use With Separate Wearing Course; and
CAN/CGSB – 37.58-M86, Membrane, Elas –
tomeric, Cold-Applied Liquid for Nonexposed
Use in Roofing and Waterproofing. These
standards do not contain maximum values
for vapor permeance, requirements for
reporting inverted wet-cup permeance
numbers, or osmosis-testing requirements.
Based on the field observations and the
testing performed in this study, the existing
standards do not have adequate test
requirements to prevent premature blistering
of polyurethane membranes.
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DE C E M B E R 2010 I N T E R FA C E • 2 9
RECOMMENDATIONS
Awareness and understanding of the
physical process of osmosis and its potential
impact on building materials will help
the industry come up with solutions and
avoid the problem in the future.
We recommend that maximum allowable
values for membrane vapor permeance,
tested under inverted-wet-cup conditions,
and osmosis testing requirements be
included in current industry standards referenced
by polyurethane membrane manufacturers,
specifically ASTM C836-00 and
CAN/CGSB–37.58-M86.
We also recommend that an industryaccepted
standard be developed to test new
IRMA roofing and waterproofing membranes
for susceptibility to osmotic flow.
Additional research is needed to determine
allowable osmotic- and vapor-flow rates
that can be safely accommodated by moisture
flow through concrete slabs. The
effects of aging and exposure to wet and
alkaline conditions on the material properties
of polyurethane membranes in the field
should also be further researched in this
context. Research should also be performed
to examine the effects of concrete primers
and sealers to prevent the passage of salts
to the membrane interface.
Based on these findings, new poly ure –
thane membranes should be modified to be
sufficiently impermeable to vapor and
osmotic flow to prevent blistering within
their expected service lives, while still
maintaining their other desirable physical
properties for waterproofing.
ACKNOWLEDGEMENTS
We thank Mark Lawton, PEng, of
Morrison Hershfield, Ltd.; Bob Matich of
BASF Canada; and Cor Claus at Pacific
Polymers for their assistance and support
during this research project.
REFERENCES
ASTM Standard E96/E96M-05, Stan –
dard Test Methods for Water Vapor
Transmission of Materials, ASTM
International, 2005.
ASHRAE Handbook of Fundamentals,
American Society of Heating, Re frig –
erating and Air-Conditioning Engi –
neers, Inc., Atlanta, GA, 2005.
Lenntech, Osmotic Pressure Calculator,
available at www.lenntech.com,
2008.
S. Onmura, S. Hokoi, T. Matsushita, D.
Ogura, K. Kominami, Y. Yasui, “A
Measurement of Concrete Hygro –
thermal Properties and the Influence
of Its Scattering on Hygrothermal
Behaviour in Concrete Walls,” ASTM
Second Symposium on Heat-Air-
Moisture Transport: Measurement
and Implications. Vancouver, BC,
2009.
D. Oxtoby, H. Gillis, N. Nachtrieb, Prin –
ciples of Modern Chemistry, 4th
Edition, Saunders College Publishing,
1999.
Kyoji Tanaka, Structural Engineering
Research Center, Tokyo Institute of
Technology, e-mail discussion re –
garding blistering of fluid-applied
polyurethane membranes, 2008.
Kyoji Tanaka and Hiroyuki Miyauchi,
“Waterproofing Systems in Japan,”
Interface, RCI, Inc., October 2007.
Wikipedia, osmosis definition at
www.en.wikipedia.org, 2009.
WUFI Pro 4.2 IBP Material Database,
Fraunhofer Institut Bauphysik,
2009.
Brian Hubbs, PEng, a senior building science specialist with
RDH Building Engineering Ltd., has over 18 years of experience
as a consultant focused exclusively in the field of building
science. This work has included the design of new building
enclosures as well as forensic investigation, rehabilitation,
maintenance, and litigation support on existing buildings.
Hubbs’s experience includes steep- and low-slope roofing
systems, wall cladding of all types, windows, glazing,
glass/metal curtain walls and skylights, and below-grade and
plaza waterproofing systems. He is a Building Envelope Professional (BEP) through the
Architectural Institute of British Columbia Professional Engineers and Geoscientists
(IBC/APEGBC) program.
Brian Hubbs, PEng, BEP
Graham Finch is a building science research engineer with
RDH in Vancouver, BC. He holds a master’s degree specializing
in building science from the University of Waterloo and is
actively involved with numerous research projects at RDH,
leading to several papers. Finch has several years of experience
as an engineering consultant on building enclosure
issues across North America. This work has included new
construction design, hygrothermal modeling, material evaluation
and testing, forensic investigation, whole building monitoring,
and several industry research studies.
Graham Finch
Robert Bombino, PE, senior science specialist and principal
with RDH, has extensive experience with a variety of building
enclosure systems, components, and materials used across
the U.S. and Canada. Prior to joining RDH in Seattle in 2004,
Robert spent five years practicing in Boston, MA. He holds a
bachelor’s degree in civil engineering from the University of
Waterloo and a master’s in architectural engineering from
Penn State University. He is a registered professional engineer
in Massachussets and Washington and a member of
ASTM Committees C16, D08, and E06, as well as a member
of ASHRAE Technical Committee 4.4.
Robert Bombino, PE
30 • I N T E R FA C E DE C E M B E R 2010