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466 Clean 2009, 37 (6), 466 – 474

Chuck Yu1
Derrick Crump2
Research Article
Veronica Brown3
Exposure Risk Assessment of the Emissions of
1
Enviro-Act Consultants Ltd., Milton
Keynes, UK.
Wood Preservative Chemicals in Indoor
2
Cranfield Health, Cranfield University, Environments
Bedfordshire, UK.
3
BRE, Watford, UK. A collaborative study was undertaken to evaluate the sustainability of a new genera-
tion of biocides for the treatment of timbers in buildings and to validate the recycla-
bility of the treated timbers. The evaluation included an assessment of the impact of
emissions of the wood treatment chemicals during the service life of timbers and
recycled wood based products. This involved emission testing of active substances
(propiconazole, tebuconazole, permethrin and dichlofluanid) and volatile organic
compounds (VOCs) from timber pretreated or coated using formulated products. The
German AgBB method for evaluating VOC emissions from construction products was
used to discuss the relative risk of the treated timbers. The emission rates of the active
substances from the treated timbers were compared to the ADI (Acceptable Daily
Intake) values given in the draft reports from the EU Biocides Directive, 98/8/EC, to
determine the exposure risk to building occupants. As a part of this study, the emis-
sions of the active substances from the stud frame of a newly built test cabin were
monitored over a two year period.
Keywords: Emissions testing; Exposure risk assessment; Indoor Air; Volatile organic compounds
(VOCs); Wood preservatives;
Received: March 2, 2009; revised: April 22, 2009; accepted: April 28, 2009
DOI: 10.1002/clen.200900046

1 Introduction Previous studies in Germany [2], USA [3] and by BRE (Building
Research Establishment Ltd.) [4] could provide a guide for the devel-
According to EU Biocides Directive 98/8/EC (May 2000), exposure opment of an exposure risk assessment. However, it should be noted
risk assessment should form an integral part of risk assessment for that these studies were based on PCP (pentachlorophenol) and lin-
a biocidal product for regulatory purposes. Preferably, representa- dane formulations that are being phased out of the market and also
tive data from well designed field studies should form the basis for other types of biocides that are not relevant to the current wood
the review, registration, evaluation and risk assessment of the treatment market in the UK. The volume of wood preservatives used
chemicals. For some biocidal products, the data connected with the in the German and US studies was related to in situ applications
release of the active ingredients to soil and water during the differ- (e. g., by spraying and brush on coating) and this would not be rele-
ent stages of the products life cycle has been assessed by EU and vant to the pretreatment products used in UK homes. The pre-
industry sponsored projects. However, the emissions to air of bio- treated timbers (e. g., in trusses and timber frame houses) are
cides from products installed in service, e. g., in buildings, have not expected to have much lower amounts of wood preservatives
yet been fully assessed to provide sufficient data for exposure risk released by evaporation in the indoor environment. The German
assessment. The objective of this study was to assess the sustainabil- studies largely related to interior room paneling, treated by occu-
ity of a new generation of wood protection and wood care products pants with surface applied products over many years. The spray and
for the treatment of timbers for buildings by considering the brush on applications would release much higher concentrations.
impact of emissions to air of wood treatment chemicals from The USA study included assessment of exposure to termiticides used
treated timbers, especially during the service life of the products [1]. post construction for curative treatments.
Exposure risk assessment is recommended by the OECD (Organiza- For biocides with low vapour pressure, some emissions to indoor
tion for Economic Cooperation and Development) (see following air over a long period may be expected. SVOCs (semi volatile organic
websites: www.oecd.org/document/53/0,2340,en_2649_201185_18 compounds) such as pesticides are readily retained on surfaces (sink
97781_1_1_1_1,00.html and www.oecd.org/findDocument/0,2350, effects). Their re-emission from sinks could potentially occur for
en_2649_34383_1_119820_1_4_1,00.html). months or years after application. Preservatives for structural tim-
ber have to be effective for decades, so their active ingredients are
expected to persist in the treated wood. Residues of pesticides found
Correspondence: Dr. C. Yu, Enviro-Act Consultants Ltd., 29 The Nortons, in indoor air, homes and on floors and other surfaces contribute to
Caldecotte, Milton Keynes, MK7 8HQ, UK.
E-mail: chuck.yu@btinternet.com the overall exposure of the household occupants. Many studies,

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Clean 2009, 37 (6), 466 – 474 Exposure Risk Assessment of Wood Preservatives in Indoor Environments 467

Table 1. Timber treated with formulated products for emission testing.

Pretreated (double vacuum impregnation) spruce


1. Pine pretreated with solvent based propiconazole/tebuconazole/permethrin/IPBCa) (P6)
2. Pine pretreated with a water based propiconazole/tebuconazole/permethrin (P3)
3. Spruce pretreated with solvent based propiconazole/tebuconazole/permethrin/IPBC (S10)
4. Spruce sample pretreated with a water based copper/propiconazole/tebuconazole (S4)

Woodcare coating, brush on applied on Scots pine


5. Pine sample coated with woodstain (teak) containing the active substance, dichlofluanid
6. Pine sample coated with a quick dry formulation containing propiconazole and flurox
7. Pine sample coated with acypetacs zinc and permethrin
8. Untreated Scots pine (P13)
9. Untreated Spruce (S13)
a)
3-iodo-2-propynyl butylcarbamate (IPBC).

including those cited, have assessed exposure to pesticides used microchambers were placed in a constant temperature room (238C).
indoors, sometimes for many years after the building was com- Clean air was supplied to the microchamber using a zero air genera-
pleted. This study focuses on wood preservatives impregnated into tor. A proportion of the zero air was humidified by passing through
wood which are used in construction as stud and structural frames a deionized water bubbler, and then mixing with the zero air to pro-
in housing, as well as wood care products, e. g., wood stain on win- vide 50% relative humidity in the air supply. The airflow was regu-
dow frames. lated to ensure a flow of 0.03 m3/h through the microchambers
when testing the timber samples. The quality of the air supply
through an empty chamber was determined prior to emissions test-
2 Methods ing. The total airflow (0.03 m3/h) was sampled for the determination
of the emissions of the wood preservatives propiconazole, tebucona-
BRE 2 L microchambers were used for the assessment of emissions zole, permethrin, dichlofluanid and other newly developed active
to air of wood preservative chemicals from timbers treated with for- substances (SVOCs) at the outlet using a polyurethane foam (PUF)
mulated products. The emission testing of a duplicate sample of sampler in a brass cylindrical capsule. The sampling airflow rate,
spruce timber treated by double vacuum impregnation has been i. e., the rate of air passing from the chamber outlet into the brass
previously reported [5]. The previous paper also reported a one year capsule containing the PUF sampler, was monitored and measured
monitoring study of the emissions of active substances from a using a PrimeAir calibrator throughout the sampling period of up
treated timber frame of a test cabin. This paper reports the emis- to 337 h (l10.11 – 10.70 m3 of air). Due to the low volatility of the
sions of wood preservatives and VOCs from four samples of pre- active substances, the sampling was carried out over 5 to 10 day
treated timbers (spruce and Scots pine) and three coated pines; and periods as follows, 3 – 8, 28 – 35, 55 – 65 and 85 – 90 days after expo-
the results of two years monitoring of a test cabin (27 m3) con- sure of the treated timber. Gas chromatography/mass spectrometry
structed using prefabricated wall panels and a treated timber (GC/MS) was used for the analysis of propiconazole, tebuconazole
frame. The evaluation of VOC emissions was based on the 2008 ver- and permethrin [1].
sion of AgBB (German Committee for Health-related Evaluation of An area specific airflow rate of 0.9 m3h – 1m – 2 was used for the test-
Building Products) (see: www.umweltbundesamt.de/building-prod ing of the pretreated timber and 1 m3 h – 1 m – 2 was used for the tim-
ucts/archive/AgBB-Evaluation-Scheme2008.pdf). ber coated with wood care products. These area specific airflow
rates were used as worst case examples of a small room built with a
timber floor, as given by EN ISO 16000-9: 2006. Coatings are nor-
2.1 Environmental Chamber Test
mally applied to exposed timber beams, floors, windows and doors
The treated timbers that were tested are shown in Tab. 1. and other wood trims inside a room, whereas pretreated timber
The pretreated timber stud was prepared by vacuum impregna- would normally be used as studs and these would be covered by plas-
tion by Arch Timber Protection according to the normal practice for terboard in an occupied environment (e. g., in the living room of a
preparation of timbers for the housing market in the UK. The house). A reduced area specific airflow rate was therefore selected
treated timber was cut to the dimensions required for emission test- for the testing of the pretreated timber products.
ing by Arch and sealed by wrapping in aluminum foil and delivered VOCs were sampled using Tenax adsorbent tubes and determined
to BRE for testing. The sealed samples were tested in microchambers as described by EN ISO 16000-9: 2006. For timber treated with the
immediately after exposure. The dimensions of the timber samples water based formulation, a sampling flow rate of 0.009 m3/h for a
were 0.06 x 0.2 x 0.02 m. period of about 0.5 h was used and for timber treated with a solvent
The formulated wood care products, as supplied by the industrial based product, a sampling flow rate of 0.003 m3/h for 1 min was
partner (ICI Paints), were brush applied on all sides of a Scots pine used. The sampling of VOCs was carried out after 3 and 28 days of
timber panel available in the laboratory (0.06860.260.2 m). The exposure of the pretreated timber. The air sampling and analysis
amounts applied were as follows; 2.4 g of wood stain (teak), 5.7 g of a was as prescribed by the international standard, ISO 16000:6 using
,
quick dry formulation and 4.9 g of a low odour’ product. GC/MS for identification of compounds and FID (flame ionization
The treated timber pieces were tested in the BRE microchambers detector) for quantification. The German AgBB method was used for
[5, 6]. The microchamber had a 2 L stainless steel cylindrical com- the evaluation of the related exposure risk of treated timbers for
partment for loading the test specimen for emission testing. The building occupants. The evaluation as prescribed by AgBB requires

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468 C. Yu et al. Clean 2009, 37 (6), 466 – 474

Figure 1. The air change rate and temperature conditions during January 2005 to March 2007.

the testing of timbers using a standard environmental chamber throughout the period. While the window and door were being pre-
according to the international standard, EN ISO 16000-9. For this pared by Osmose (an industrial partner to the project) in March –
evaluation, a BRE microchamber was used to determine the concen- July 2005, the window opening was temporarily sealed on 1 April
trations of VOCs emitted from the treated timbers. The area specific 2005 with polyacrylic sheeting and the door opening was sealed
airflow rates used were as described above. with acrylic coated plywood.
During the period from October to December 2005, a window was
delivered to BRE from Osmose (on 7 October 2005) and was fitted to
2.2 The Test House Study
the test cabin on 11 October 2005. The door was delivered to BRE on
A test cabin was constructed to simulate a living room (27 m3) of a 25 November and was fitted to the test cabin on 28 and 29 Novem-
newly built house. The treated timber (using water based tebucona- ber 2005. After fitting the window and door to the test cabin, heat-
zole, propiconazole and permethrin) was used to construct a frame ing was turned on and was thermostatically controlled at 238C. The
and cavity into which phenolic foam was injected for thermal insu- monitoring of emissions of active substances was undertaken before
lation. This was covered by cement particleboard to form the prefab- and after the fitting of the window and door. The air exchange rate,
ricated wall panel, as manufactured for the housing market in the temperature and relative humidity in the test cabin were also
Europe. The frame effectively acted as studs (300 mm centers) for a monitored. The one year monitoring period (first and second phase)
timber framed house. The materials were chamber tested to deter- of the test cabin has been reported previously [5].
mine the emissions of VOCs and wood preservatives. The third phase of monitoring involved the fitting of plaster-
The test cabin was built at BRE on 7 December 2004 by Space4 Ltd. board to the test cabin on 29 March 2006. A wood stain coating (sup-
(a subsidiary of Westbury Homes). The emissions of active substan- plied by ICI Paints) was applied to the window and door of the test
ces from the treated timber stud were monitored to provide data for cabin on 2 October 2006. The mean four week air change rate in the
a modeling study to determine the fate of active substances in the test cabin was monitored every month by a tracer gas method [7],
indoor environment. The first phase of the study started after the during the two year period.
construction of the test cabin, without the plasterboard cladding of The emissions of the wood preservatives tebuconazole, propicona-
the wall panel, the window or door. The objectives of the monitor- zole and permethrin were sampled about once a month throughout
ing study have been described [1]. The test cabin was built to simu- the two year study, using PUF samplers, over a sampling period of
late the living room (or bedroom) of a home. The main purpose of five days and a sampling rate of 0.275 m3/h. Formaldehyde and
this test house study was to provide realistic data for exposure risk TVOC concentrations in the test cabin were also monitored by diffu-
assessment of the emissions of active substances from wood preser- sive methods. Diffusive measurement of formaldehyde (ISO 16000-
vative treated timbers in a timber framed house. 4) was undertaken using a badge (GMD 570) containing a 2, 4-dini-
During the first period from January to March 2005, the window trophenylhydrazine coated filter paper. The badge was exposed for
and door openings were covered with plastic (polyethylene) tarpau- three days to provide a three day average measurement in the test
lin. The emissions of wood preservatives, propiconazole, tebucona- cabin. After sampling, the badge was solvent desorbed with acetoni-
zole and permethrin in the test cabin were monitored by air sam- trile and then analyzed by high performance liquid chromatogra-
pling using PUF samplers. The air exchange rate of the test cabin phy (HPLC). Tenax TA adsorbent tubes were used to determine the
was also monitored (in duplicate) by a tracer gas method [7]. The 28 day average exposure by diffusive air sampling according to BS
temperature and humidity of the test cabin were monitored EN 16017-2:2003, Part 2.

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Clean 2009, 37 (6), 466 – 474 Exposure Risk Assessment of Wood Preservatives in Indoor Environments 469

Figure 2. Concentrations of active substances monitored during January 2005 to March 2007.

Figure 3. TVOC concentrations in the test cabin from January 2005 to March 2007.

3 Results of the active substances, propiconazole, tebuconazole and perme-


thrin monitored in the test cabin from January 2005 to March 2007
The two year test cabin study showed the concentrations of active are shown in Fig. 2. The concentrations of TVOC and formaldehyde
substances were consistently close to the quantitation limits of are shown in Fig. 3 (TVOC) and Fig. 4 (formaldehyde).
about 2 to 8 ng/m3 for a 40 to 50 m3 air sample and less than 10 ng/ The results of the environmental chamber test of the emissions of
m3, except for propiconazole in the first month (13 ng/m3). The air active substances from pretreated timbers are shown in Tab. 2 and
change rate in the test cabin was monitored (in duplicate) every the emissions from coated timbers are shown in Tab. 3. The emis-
month and the temperature and humidity were continuously moni- sions of VOCs from the pretreated timbers after 3 and 28 days of
tored. These measurements are shown in Fig. 1. The concentrations chamber tests are shown in Tabs. 4 and 5 which also includes the

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470 C. Yu et al. Clean 2009, 37 (6), 466 – 474

Figure 4. Formaldehyde concentrations in the test cabin from January 2005 to March 2007.

assessment of the relative risk factors for the individual compounds The results of air monitoring of active substances from the test
as required by the AgBB method. cabin were at or below the limit of quantitation (a 10 ng/m3). Fitting
the window and door and the application of wood stain did not
cause any significant effect on the cabin air concentrations of active
substances. However it is worth evaluating these results and com-
4 Discussion paring them to acceptable daily intakes.
Low emission rates of active substances were shown by emission The total air volume in the test cabin was 27 m3 and the concen-
testing of the treated timber studs prepared by double vacuum trations of the active substances were consistently below 10 ng/m3,
impregnation of water and solvent based wood preservatives con- except during the first month of monitoring. A normal adult weigh-
taining propiconazole, tebuconazole and permethrin. These were ing 60 kg is deemed to reside in a room for 18 h a day and during
consistent with measurements reported by other workers using PUF that period will inhale 18.5 m3 of air and about 185 ng of active sub-
samplers [8, 9, 10]. Most of the emission rates measured, were close stance per day. The exposure per kg body weight (bw) would be
to quantitation limits. about 3.083 ng kg – 1 bw day – 1, or approximately 0.000003 mg kg – 1
A low emission rate for wood preservatives was expected as the bw day – 1.
active substances interact with wood lignin (fixation), which is a Active substances have acceptable daily intakes (ADI) or accept-
necessary process for the biocides to function effectively as preserva- able operator exposure levels (AOEL) as shown in the draft reports
tives [11, 12]. Lignin is a highly cross-linked, amphiphilic biopoly- under the EU Biocidal Products Directive. The exception is perme-
mer with different phenyl-propanoid units connecting to various thrin as the draft report for this substance has not been published
ester bonds. There are many possible arrangements of lignin macro- yet. Permethrin has been extensively studied as a crop protection
molecules in the surface layer. These can form hydrogen and other substance and its ADI is well established.
non-covalent bonds, and due to their ester bonds, many different (i) Tebuconazole, ADI = 0.03 mg kg – 1 bw day – 1, based on a one
transformations are possible which affect the molecular sizes and year dog study with a NOAEL (no observable adverse effect level)
volumes due to interactions at the air-water interface of the wood of 3 mg kg – 1 day – 1 and an uncertainty factor of 100.
surface [13, 14]. Lignin is highly cross-linked due to the polymeriza- (ii) Propiconazole, AOEL = 0.08 mg kg – 1 bw day – 1, based on a two
tion of substituted phenolic components, monolignols, catalyzed generation study with a NOAEL of 8 mg kg – 1 day – 1 and an
by the enzyme peroxidase. This could be influenced by the cellulose uncertainty factor of 100.
substrates and solution media leading to assembly systems, provid- (iii) IPBC (3-iodo-2-propynyl-butylcarbamate), AOEL and ADI both
ing pores and channels that would allow diffusion of molecules to given as 0.2 mg kg – 1 bw day – 1.
take place on the surface [15]. The low vapor pressure of wood pres- (iv) Dichlofluanid, AOEL = 0.2 mg kg – 1 bw day – 1, the secondary
ervatives can be an important factor which determines the emis- long term exposure is given as 0.025 mg kg – 1 bw day – 1, based
sions and fate of active substances in the indoor environment [16, on a NOAEL of 20 mg kg – 1day – 1 and an uncertainty factor of
17]. The timber species and the depth of penetration of the wood 100.
preservative could have a significant effect on the emissions of the (vi) Permethrin, ADI = 0.05 mg kg – 1 bw day – 1, based on a NOAEL of
active substances [18]. 5 mg kg – 1 day – 1 and an uncertainty factor of 100.

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Clean 2009, 37 (6), 466 – 474 Exposure Risk Assessment of Wood Preservatives in Indoor Environments 471

Table 2. Emissions of wood preservative active substances from pre- The lowest ADI/AOEL is the secondary long term exposure value
treated timber. for dichlofluanid of 0.025 mg kg – 1day – 1. Therefore, 0.00000308/
0.0256100 = 0.0123% of the ADI. The ADI/AOEL for the other sub-
Wood Emission rates, ng m – 2h – 1 (microchamber test)
preservative stances is of the same order, so similar values would result.
The results showed that the exposure to active substances from
1. Scots pine pretreated with solvent based propiconazole/tebucona- treated wood in indoor air during the first two years after comple-
zole/permethrin/IPBC (P6) tion was low and that a tiny fraction of the acceptable daily intake
3 – 10 days 28 – 34 days 56 – 61 days 79 – 90 days would result. Even where a number of active substances may be
Propiconazole 54 63 45 45
used in a formulation, and if all had similar effects, the combined
Tebuconazole 18 27 27 27
Permethrin 18 18 27 27 exposure would still be of very low significance.
IPBC ND ND ND ND The results have shown that emission rates of active substances
from the pretreated timbers were negligible compared to the ADI
2. Pine pretreated with a water-based propiconazole/tebuconazole/ (Acceptable Daily Intake) values given in the draft reports from the
permethrin (P3) EU Biocidal Directive and should not be a concern as an inhalation
3 – 10 days 28 – 34 days 56 – 61 days 79 – 90 days
Propiconazole 27 27 33 27 exposure risk to building occupants.
Tebuconazole 18 18 20 18 The TVOC concentrations monitored in the test cabin, showed an
Permethrin 20 27 33 27 initial high concentration, 1471 lg/m3 due to the emission of C5 – C7
alkanes and toluene, mainly from the foam insulant and other nat-
3. Spruce pretreated with solvent based propiconazole/tebuconazole/ ural products such as butanal, hexanal, a-pinene, limonene and hex-
permethrin/IPBC (S10)
anoic acid. TVOC concentrations declined to 90 to 130 lg/m3 after
3 – 10 days 28 – 34 days 56 – 61 days 79 – 90 days
Propiconazole 108 144 85 90 three months, which is below the 50 percentile value of TVOC con-
Tebuconazole 45 48 27 27 centrations monitored by a BRE survey of 870 homes [19] and below
Permethrin 27 32 27 27 the recommended value of 200 to 300 lg/m3 for good indoor air
quality [20]. The concentration rose to 271 and 876 lg/m3, soon after
4. Spruce sample pretreated with a water based copper/propicona- the window was fitted to the test cabin in October 2005 and rose
zole/tebuconazole (S4)
again to 4846 lg/m3 after fitting the door. The high TVOC concentra-
3 – 10 days 28 – 34 days 56 – 61 days 79 – 90 days
Propiconazole a 18 18 20 a 18 tion was mainly attributed to white spirit solvent chemicals, possi-
Tebuconazole a 18 18 20 a 18 bly from the coating on the door. The lower air exchange rate also
Permethrin a 18 18 20 a 18 contributed to the increase in TVOC concentration. The concentra-
tion declined to the acceptable level (a 300 lg/m3) during February
8. Untreated Scots pine (P13) and March 2006 but rose again when the plasterboard was fitted
3 – 10 days 28 – 34 days 56 – 61 days 79 – 90 days
Propiconazole a 18 a 15 a 18 a 18 (June 2006) and when wood stain was applied to the window and
Tebuconazole a 18 a 15 a 18 a 18 door (October 2006). The concentration declined to below 200 lg/m3
Permethrin a 18 a 15 a 18 a 18 from November 2006 to March 2007.
The formaldehyde concentration monitored in the cabin was
9. Untreated Spruce (S13) within the normal range (geometric mean: 30 lg/m3) as shown by
3 – 10 days 28 – 34 days 56 – 61 days 79 – 90 days
the BRE survey of 870 homes [19] in England. These studies also
Propiconazole a 17 a 15 a 18 a 18
Tebuconazole a 17 a 15 a 18 a 18 showed an increase in formaldehyde concentration during summer
Permethrin a 17 a 15 a 18 a 18 as the temperature in the cabin reached 268C (maximum). The form-
aldehyde concentration fell to 20 lg/m3 during autumn, specifically

Table 3. Emissions of wood preservative active substances from coated Scots pine.

Wood preservative Emission rates, ng m – 2h – 1 (microchamber test)

5. Pine sample coated with woodstain (teak) containing active substance, dichlofluanid
3 – 10 days 28 – 34 days 56 – 61 days 79 – 90 days
Dichlofluanid a 20 a 20 a 20 a 20

6. Pine sample coated with a quick dry formulation containing propiconazole and flurox
3 – 10 days 28 – 34 days 56 – 61 days 79 – 90 days
Propiconazole a 18 ng m – 2h – 1 a 18 ng m – 2h – 1 a 18 ng m – 2h – 1 a 18 ng m – 2h – 1
Fluroxa) 1 lg m – 2h – 1 7 lg m – 2h – 1 6 lg m – 2h – 1 a 2 lg m – 2h – 1

7. Pine sample coated with acypetacs zinc and permethrin


3 – 10 days 28 – 34 days 56 – 61 days 79 – 90 days
Permethrin a 18 ng m – 2h – 1 a 18 ng m – 2h – 1 a 18 ng m – 2h – 1 a 18 ng m – 2h – 1
Acypetacs 553 lg m – 2h – 1 460 lg m – 2h – 1 NMb) NMc)
a)
Flurox was analyzed by HPLC; the detection limit was about 2 lg m – 2 h – 1 in an 8 m3 air sample.
b)
ND = not detected; NMc) = not measured. The quantitation limit for propiconazole, tebuconazole and permethrin was about 18 ng m–2
h–1 in an 8 m3 air sample.

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472 C. Yu et al. Clean 2009, 37 (6), 466 – 474

Table 4. Concentrations of VOCs emitted from the pretreated timbers after three days.

Compound Concentration, lg/m3 (microchamber test)

P3 P6 P13 S4 S10 S13


Acetonitrile (3.2)a) (a 1.0) (1.7) (a 1.0) (a 1.0) (a 1.0)
n-Heptane 1.7 a 1.0 2.1 1.6 a 1.0 1.0
Pentanal a 1.0 12.3 a 1.0 a 1.0 a 1.0 a 1.0
n-Octane 1.5 a 1.0 2.6 2.1 a 1.0 1.0
Hexanal a 1.0 37.0 a 1.0 a 1.0 a 1.0 a 1.0
Pentan-1-ol 6.2 3.9 6.1 a 1.0 a 1.0 a 1.0
n-Nonane a 1.0 20.6 1.5 a 1.0 1.1 a 1.0
a-pinene 1.0 30.4 0.7 a 1.0 a 1.0 a 1.0
C10 – C12 alkanes and aromatics NDb) (4,530) ND ND (184) ND
OMCTS a 1.0 a 1.0 1.7 a 1.0 a 1.0 a 1.0
n-Octanal 5.0 ND 3.4 a 1.0 ND a 1.0
Hexanoic acid 22.4 a 1.0 17.0 a 1.0 a 1.0 3.1
n-Nonanal 1.8 ND 2.5 2.7 ND 1.9
n-Decanal a 1.0 ND 2.8 1.9 ND 1.1
TVOCFIDc) 37.9 4,690 44.7 21.5 189 13.9
TVOCFID AgBBd) 13.7 4,590 11.9 a 5.0 41.1 a 5.0
a)
Compounds for which concentration values appear in brackets, acetonitrile and the range of hydrocarbons, had no available response
factor and so the calibration for toluene has been applied.
b)
ND = not detected, for n-octanal, n-nonanal and n-decanal it is possible that small amounts may be obscured by the range of hydrocar-
bons present.
c)
The TVOCFID value was that obtained using ISO16000-6, i. e., the sum of VOCs eluting between and including n-hexane and n-hexadecane,
quantified as toluene.
d)
The TVOCFID AgBB value is that obtained using the September 2008 version of the AgBB, also quantified as toluene, but only summing
those compounds with a concentration A 5 lg/m3.

Table 5. Concentrations of VOCs from the pretreated timbers after 28 days of exposure.

Compound Concentration, lg/m3 (microchamber test)

P3 P6 P13 S4 S10 S13


Pentanal 3.2 3.8 3.5 a 1.0 a 1.0 2.1
n-Octane a 1.0 a 1.0 a 1.0 a 1.0 2.2 a 1.0
Hexanal 12.5 (Ria) = 0.014) 6.8 (Ri = 0.008) 13.7 (Ri = 0.015) a 1.0 a 1.0 3.3
Pentan-1-ol 5.2 (Ri = 0.0014) a 1.0 5.6 (Ri = 0.0014) a 1.0 a 1.0 a 1.0
n-Nonane a 1.0 4.2 a 1.0 a 1.0 a 1.0 a 1.0
a-pinene a 1.0 3.8 a 1.0 a 1.0 a 1.0 a 1.0
C10 – C12 alkanes and aromatics NDb) (587)c) ND ND (21.9) ND
n-Octanal a 1.0 ND 1.1 a 1.0 ND a 1.0
n-Nonanal 1.2 ND 1.9 a 1.0 ND a 1.0
n-Decanal a 1.0 ND 1.3 a 1.0 ND a 1.0
TVOCFIDd) 18.2 590 21.1 2.5 28.3 4.4
TVOCFID AgBBe) 12.3 409 13.4 a 5.0 a 5.0 a 5.0
a)
Ri is the relative risk factor for the individual compounds defined by the AgBB as Ri = Ci/LCIi where Ci is the concentration of the individ-
ual VOC and LCI is the lowest concentration of interest.
b)
ND = not detected, for n-octanal, n-nonanal and n-decanal it is possible that small amounts may be obscured by the range of hydrocar-
bons present.
c)
Compounds for which concentration values appear in brackets, acetonitrile and the range of hydrocarbons, have no available response
factor and so the calibration for toluene has been applied.
d)
The TVOCFID value is that obtained using ISO16000-6, i. e., the sum of VOCs eluting between and including n-hexane and n-hexadecane,
quantified as toluene.
e)
The TVOCFID AgBB value is that obtained using the September 2008 version of the AgBB, also quantified as toluene, but only summing
those compounds with a concentration > 5 lg/m3.

in September. The low air exchange rate in the cabin and the treated timbers were less than 1. There were no carcinogens
summer temperature could have affected the concentration during detected and the TVOC concentration was less than 10 mg/m3 after
the summer of 2006. Fitting the window, door and plasterboard three days of exposure and less than 1 mg/m3 after 28 days. All the
also affected the formaldehyde concentration in the cabin but the unidentified compounds and compounds that do not have a LCI
concentration was consistently below the WHO guideline value of (Lowest Concentration of Interest) value under the current AgBB
0.1 mg/m3 [21]. procedure were present at concentrations below 5 lg/m3. TVOC con-
The evaluation of emissions of VOCs have shown that the total rel- centrations emitted from the treated Scots pine and spruce timber
P
ative exposure risk values (R = Ri) due to emissions from pre- that used solvent based formulations were shown to be dominated

i 2009 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim www.clean-journal.com


Clean 2009, 37 (6), 466 – 474 Exposure Risk Assessment of Wood Preservatives in Indoor Environments 473

by aliphatic and aromatic hydrocarbons. VOC emissions from the tives to soil and water to determine the possible impact on ecology
treated timbers containing either solvent based or water based and the aquatic environment; (ii) the determination of exposure via
wood preservatives, were shown to pose a low risk to occupants of dermal contact and ingestion, as well as by inhalation and (iii) an
buildings. assessment of the possible intake of active substances via particu-
Previous testing of untreated and treated spruce samples showed lates and dusts.
a higher TVOC emission rate from the control spruce (untreated)
sample in comparison to the treated spruce sample [1]. This could
be due to the loss of VOCs during vacuum treatment when the wood
Acknowledgements
preservatives, carried by water are applied using pressure to the
spruce timber, or it could be due to the fixation of preservatives to The authors thank John Rowley of BRE for analysis of wood preserva-
the wood, inhibiting the release of VOCs from natural products. The tives, The Sustainable Development & Regulatory Directorate,
testing of pretreated timber samples reported in this paper showed Department for Business Enterprise & Regulatory Reform (BERR),
a low emission of VOCs in Tabs. 4 and 5 except for the spruce timber UK, for funding and the British Wood Preserving and Damp Proof-
sample (P6) treated with a solvent based wood preservative. ing Association including ICI Paints and Arch Timber Protection
Although emissions of terpenes are expected from timbers, an Limited for their collaboration and support for this project.
uncharacteristically low emission of terpenes was shown by all the
samples including the untreated spruce and pine samples. This may The authors have declared no conflict of interest.
be due to the treatment and kiln drying process of the timber or the
exposure condition of the timbers prior to emissions testing.
The emission of terpenes would depend on the condition of the
timber available; a-pinene was consistently found in all the timbers References
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