Recent University
Study Documenting the Ineffectiveness of Bleach on Killing Mold on Wood
Ability of bleach and
other biocide treatments to remove and prevent mold growth on Douglas-fir
lumber
by Adam M. Taylor, Camille M. Freitag, and
Jeffrey J. Morrell
Molds are an increasingly important issue for all
building materials, including wood. While washing with bleach is a commonly
recommended method for removing molds, and the associated discolorations,
there is surprisingly little information on the effectiveness of this
treatment. The ability of mold removal treatments to brighten wood and
eliminate fungi was assessed on Douglas-fir (Pseudotsuga menziesii) sap wood
lumber heavily colonized with mold and sapstain fungi. The boards were
subjected to different washing treatments: wiping with bleach solution,
wiping with water, and a no-wash control. Samples were evaluated visually
for changes in mold appearance and then fungi were isolated from the surface
of the wood. Replicates from the various wash treatments were further
treated with three biocide formulations. The effect of the mold control
treatments on visual appearance and fungal diversity was assessed 1 month
after treatment. Increasing bleach concentrations from 2.5 up to 20 percent
solution had no effect on the appearance of the wood following the wash
treatment, nor did such treatments completely eliminate fungi from the wood
surface. The chemical mold prevention treatments tested were not effective
in sterilizing the wood, nor did they improve the visual appearance.
From the moment it is cut in the forest until it
dries to moisture levels below 20 percent (wt./wt.), wood remains
susceptible to colonization by a variety of molds, sapstains, and decay
fungi (Dowding 1970, Kaarik 1980). For many years, lumber producers limited
the risk of fungal attack by managing production to avoid long storage
periods, spraying or ponding stored logs to raise moisture levels above
those suitable for fungal growth, kiln-drying, or applying fungicides to
sawn lumber in topical treatments (Scheffer and Lindgren 1940).
These latter treatments were primarily
prophylactic, and designed to protect the wood only during the time between
sawing and when moisture contents were reduced to below 20 percent.
The decision by the U.S. Environmental Protection
Agency in the late 1980s to restrict the use of sodium pentachlorophenates,
coupled with increasing concerns over worker exposure to antistain
chemicals, led to a gradual decline in anti-sapstain chemical usage (R.C.Anderson
et al. 2002). This decline was accompanied by increased kiln capacity in the
southern United States, but many mills in the West elected to eliminate
treatment while continuing to provide green material. This approach worked
well as long as domestic customers were willing to accept moldy, stained
wood. Recently, however, several high visibility court cases have resulted
in substantial settlements because of mold on building materials, including
wood (Robbins and Morrell 2002). These actions have renewed interest in
prophylactic anti-stain treatments. There are an array of effective, less
toxic chemicals for this purpose, but these systems are not designed for
application in structures (Morrell et al. 2002).
At the same time, there has been increased
interest in methods for removing fungal discoloration on wood already
installed, as well as in treatments to limit fungal growth under these
conditions.
The authors are, respectively,
Graduate Research Assistant, Senior Research Assistant, and Professor, Dept.
of Wood Science and Engineering, Oregon State Univ., 119 Richardson Hall,
Corvallis, OR 97331. This paper was received for publication in October
2002. Article No. 9557. Forest Products Society Member. ©Forest Products
Society 2004.
Forest Prod. J.
54(4):45-49.
While wood can be colonized by an array of organisms (Hawksworth 1991), the
primary concern of many has been the "toxic mold" Stachybotrys chartarum (Johanning
et al. 1996, Fung et al. 1998, Hodgson et al. 1998, Daggett et al. 1999, B.
Anderson et al. 2002). This fungus does not appear to be associated with
freshly sawn Douglas-fir lumber (Kang and Morrell 2000), but it is primarily
found in cellulose-based materials (Ellis 1971).
A commonly recommended treatment for mold removal
is to flood the wood surface with a dilute solution of sodium hypochlorite
(bleach), and then brush the wood to dislodge spores and hyphal fragments
(Oregon Dept. of Human Services 2002). Bleach is a potent disinfectant
(Russell et al. 1982), but there is little data supporting its effectiveness
for this application. Similarly, a number of compounds are marketed that
claim to eliminate mold growth on wood, but there is little to support these
claims.
In this report, we describe tests to evaluate the
ability of bleach and/or various treatments to improve the visual appearance
of moldy wood and reduce subsequent fungal recolonization on the wood
surface.
Materials and Methods
Heavily stained Douglas-fir sapwood (Pseudotsuga
menziesii (Mirbel) Franco) boards (19 mm by 133 mm by various lengths) were
obtained from a local lumberyard. The boards had not received any prior
fungicidal treatment, and had been solid piled in storage. The boards were
cut into 89-mm-long sections that were randomly allocated to 20 treatment
groups of 10 sections each.
Wash treatments
The surface condition of each board was assessed
visually using a scale from 0 (no evidence of discoloration) to 100
(complete surface discoloration) for both surface mold and sapstain. All
visual assessments were conducted by the same person. The boards were then
treated with water or bleach diluted with water to 2.5, 5.0, 7.5, 10.0,
15.0, or 20 percent (vol./vol.). Additional sets of boards were left
untreated. In an effort to mimic normal practice with wood in vertical
exposures, the solution was wiped on the surface with a sponge, allowed to
stand for 30 seconds, and then rinsed off by dunking the piece in clean
water. The boards were allowed to dry for 20 to 30 minutes, then reassessed
for surface condition as described above. Each treatment was replicated on
10 board sections. Following visual assessment, the ability of each
treatment to kill surface fungi was assessed by pressing a 25-mm-long
section of 12-mm-wide clear plastic tape (Post-itTM tape "flags") on the
wood surface. The tape sections then were placed, face down, on 1 per cent
malt extract agar in plastic petri dishes, incubated under ambient lab
conditions (20° to 23°C), and observed for evidence of fungal growth. Fungi
were identified to genus using the appropriate taxonomic keys (Ellis 1971,
Barnett and Hunter 1972, Ellis 1976, Wang and Zabel 1990, Webster 1993). The
total number of isolations/board, as well as the number of isolations of
each genus, were noted for each treatment group.
Topical prevention treatments
The potential of three supplemental surface
treatments to limit fungal growth was examined on board sections that had
received no previous wash treatment, on boards that had been previously
washed with tap water, and on boards that had been washed with a 10 percent
bleach solution as described previously.
Boards to be treated with water-based 10 percent
disodium octaborate tetrahydrate (DOT) (Timbor, U.S. Borax, Valencia,
California) or 10 percent DOT plus ethylene glycol (Boracare, NISUS Corp.,
Nashville, Tennessee) were immersed in the treatment solution for 5 seconds,
then allowed to dry for 15 minutes. The 2 percent didecyldimethylammonium
chloride (DDAC) (Anti-Growth, Glessner Sales Incorporated, Bend, Oregon)
treatment was applied by wiping the surface with a saturated sponge.
Following treatment, the blocks were visually
assessed, and then placed in plastic bags and incubated at 32°C and 90
percent relative humidity. At the end of 4 weeks of incubation, the blocks
were again visually evaluated for discoloration, and the degree of microbial
colonization was assessed using the previously described tape method.
Results and discussion
Bleach treatments
All of the surface wash treatments re- duced the
discoloration due to molds, including the water wash (Fig. 1); however,
there was little or no difference between the treatments. The wash
treatments, including those containing bleach, had little effect on sapstain,
reducing the degree of discoloration by only 5 to 15 percent. These low
values probably reflect the relatively short residence time that the bleach
was in contact with the wood and the difficulty in degrading the complex
melanins that give the hyphae their color (Zink and Fengel 1988).
Fungal isolations were categorized on the basis of
frequency from a given set of boards for a given treatment. The majority of
fungi isolated were members of the genera Trichoderma, Penicillium, or
Graphium. The abundance of these genera on wood is typical of Douglas-fir
sapwood (Kang and Morrell 2000), and reflects the ability of these fungi to
produce prodigious numbers of spores. In addition, Zygomycetes were isolated
from many samples, although these fungi were not identified to genus.
Zygomycetes were infrequently isolated from
unwashed boards, but their frequency increased on boards washed with water
or 2.5 percent bleach (Fig. 2). Isolation levels then steadily declined with
increased bleach concentration, and no Zygomycetes were isolated from boards
treated with 20 percent bleach. Some of the wash treatments may have altered
the wood environment to favor growth by the Zygomycetes already present on
or in the wood. Isolations of Trichoderma species varied slightly with the
various treatments, but the differences were not consistent. Penicillium
species also varied inconsistently with bleach concentration. Graphium
species were isolated from all unwashed boards, and isolation levels
declined only slightly in all but one of the wash treatments. The exception
was the 15 percent bleach treatment; however, we consider this result to be
anomalous since isolation levels were high for the 7.5 and 20 percent bleach
treatments. The high incidence of Graphium isolations reflects the
adaptation of this genus for wood, as well as its ability to produce massive
amounts of sticky spores.
The isolation frequencies of the various fungi do
not imply that the boards were covered with spores or hyphal fragments;
however, the results show that viable fungal propagules remain on the wood
surface following bleach treatment. Some airborne spores also may have
landed on the boards as they were drying; however, regardless of the origin
of the fungi, failure to alter the conditions on the wood surface, primarily
through drying, will invariably lead to regrowth of these fungi.
Topical prevention treatments
Most of the boards receiving topical treatments
experienced modest increases in the degree of fungal discoloration after the
28-day incubation period (Fig. 3). It is important to remember that these
boards were heavily discolored prior to treatment, so further large changes
in discoloration were unlikely. Boards that had been washed with water or 10
percent bleach prior to treatment tended to be more heavily discolored when
they were left untreated, or treated with either boron compound, while their
appearance tended to improve slightly when DDAC was applied. Water and
bleach washes tended to reduce surface discoloration by 40 to 50 percent
(Fig. 1), but obviously they did not kill all the spores on the wood
surface; it is clear that the fungi remaining on the wood surface after
treatment were capable of continued growth and discoloration when the wood
was stored under ideal growth conditions. The DDAC treatment appeared best
able to inhibit further discoloration, a finding that supports its frequent
use as a component of anti-stain formulations.
|
Prevention treatment |
Pretreatment |
Trichoderma |
Penicillium |
Graphium |
Aspergillis |
|
Control |
Control |
50 |
10 |
80 |
0 |
|
Water |
70 |
10 |
100 |
10 |
|
10% bleach |
90 |
0 |
100 |
0 |
|
Boracare |
Control |
50 |
50 |
0 |
70 |
|
Water |
70 |
40 |
0 |
70 |
|
10% bleach |
90 |
0 |
10 |
20 |
|
Timbor |
Control |
80 |
0 |
10 |
0 |
|
Water |
70 |
0 |
10 |
10 |
|
10% bleach |
100 |
10 |
10 |
0 |
|
DDAC |
Control |
20 |
30 |
40 |
10 |
|
Water |
30 |
20 |
50 |
30 |
|
10% bleach |
50 |
40 |
10 |
10 |
Table 1. -- Isolation frequency of
various fungal genera from unwashed, water washed, or bleached Douglas-fir
sapwood boards 28 days after the application of selected topical treatment.
Isolation frequencies for Trichoderma species were generally high for all
treatments (>80% of boards), but were
highest on control (no prevention treatment) and Boracare-treated/previously
bleached boards (Table 1).
Penicillium species were far less abundant than Trichoderma in general
(Table 1), and were absent from unwashed and bleached boards treated with
Timbor, and bleached boards left untreated or treated with Boracare. DDAC
had little effect on Penicillium isolation frequency, regardless of the
pretreatment.
Although they were infrequently isolated in the
initial wash treatments test, Aspergillus species were isolated from 60
percent of the control or waterwashed boards treated with Boracare (Table
1). They were also isolated at low levels (<30%) from water-washed boards
in all four treatment groups, as well as from unwashed DDAC-treated boards.
These results suggest that incubation conditions (hot and humid) may have
favored the growth of these species.
Graphium species were isolated from all unwashed,
water-washed, or bleached boards that did not receive a subsequent
treatment (Table 1). Isolation levels of these
fungi declined sharply from boards receiving topical treatments. Isolation
levels were highest on boards treated with DDAC, ranging from 15 to 50
percent of the boards. No Graphium species were isolated from the unwashed
or water-washed boards treated with Boracare, while 10 percent of the
previously bleached boards treated with this chemical yielded such fungi.
Graphium species were isolated from each of the Timbor treatments, but the
levels were low (<20% of the boards). The dramatic decline in Graphium
frequency following topical treatments suggests that these sapstain fungi
are more easily controlled than the more abundant mold fungi.
Implications
While bleach is often recommended for remediation
of surface mold on wood, our results illustrate that the treatment does not
eliminate the surface microflora. As a result, an important component of
remediation must be drying to moisture levels below 20 percent (the
generally accepted level for inhibiting growth of fungi on wood) (Zabel and
Morrell 1992). In the absence of drying, some fungi clearly survive the
treatment and may re-colonize the surface.
The application of topical treatments also
produced variable results. None of the treatments inhibited all of the fungi
present. These treatments were selected because they are being touted as
mold treatments and because of their relatively low toxicity profiles that
would allow their use without a pesticide applicator license. However, it is
clear that these treatments lack the broad spectrum activity required to
reduce the activity of such a diverse microflora. Exploration of mixtures of
these materials is advisable.
The results highlight the difficulty of complete
removal of surface colonization by fungi and emphasize the importance of
prevention, either by kiln-drying or by the application of topical
fungicides soon after sawing.
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