1 Introduction
Numerous fungi have potential to negatively affect the performance of wood-based materials through cell wall degradation or superficial deterioration of its optical appearance. Besides various decay fungi, which can cause brown, white, or soft rot, different blue stain and mould fungi can lead to discoloration of wood. Mould fungi mostly belong to the group of fungi imperfecti and are therefore micro-fungi. Even though mould fungi do not influence the strength properties of wood-based materials (Schmidt 1994), they affect their appearance and can cause allergic responses (Sutter 2002; Robbins and Morrell 2002).
Growth of mould fungi requires a wood moisture content between 30 and 150%, temperature between 0 and 40 °C and easily accessible nutrients (Sutter 2002). Typically, mould fungi are forming surface mycelium, which can release spores through conidia.
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Mould fungi can infect nearly all materials, i.a. wood polymer composites or wood fiber insulation boards. Wood polymer composites (WPC) are composite materials made from wood, polymers such as polyethylene (PE), polypropylene (PP) and polyvinyl chloride (PVC), and different additives. The latter may be coupling agents, lubricants, fungicides or dyes. Usually, the wood percentage in WPC is 50–70% (Karus et al. 2006). Production of WPC proceeds in a continuous extrusion process or in a discontinuous injection moulding process. Typical applications of WPC are deckings, claddings, and fence elements.
Wood fiber insulation boards (WFIB) are usually made of softwood fibers obtained through thermomechanical pulping (TMP): wood chips are thermally treated with steam at high pressure and afterwards defibrillated in a refiner (Krug 2010). The boards are produced in a wet or in a dry process, where the latter is more common today. Usually polymeric methylendiphenylisocyanate (PMDI) serves as binder. Optionally, hydrophobic additives or fungicides can be added (Holzmann et al. 2012).
Different standardized test methods are available for evaluating the susceptibility of wood-based materials to mould fungi (e.g. ISO 16000-21, 2014; ASTM D 3273-00, 2000; EN 15457, 2014; EN 60068-2-10, 2006; ISO 846, 2018; EN 15101-1, 2013 and EN 15534-1, 2018). Only EN 15534-1 is related to WPC and only EN 15101-1 is related to WFIB, all others were developed for testing of building materials, plastics and coatings. Nevertheless, the purpose of this study was to compare the two mainly used standards for evaluating mould growth on wood in Europe, the British standard BS 3900—Part G6 (1989) and the ISO standard 16869 (2008), and to evaluate whether the ratings obtained correlate with each other.
BS 3900—Part G6 (1989) is usually applied to test the performance of paints on various substrates such as wood, metal, and plaster. To test panels of different wood species, Scots pine sapwood (Pinus sylvestris) is used as a reference. Painted flat panels are inoculated with a spore suspension (Aspergillus versicolor, Aureobasidium pullulans, Cladosporium cladosporioides, Penicillium purpurogenum, Phoma violacea, Rhodotorula rubra, Sporobolomyces roseus, Stachybotrys atra and Ulocladium atrum). The test takes place in an incubation chamber with optimum temperature and humidity for fungal growth. Evaluation of fungal growth proceeds via optical assessment after 28 days and rating in one of five classes. The test is extendable for up to twelve weeks. The specimens are levitating and have no direct contact with water.
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ISO 16869 (2008) serves to evaluate the effectiveness of fungistatic compounds in plastic formulations. Disc-shaped specimens are embedded in nutrient-salt agar in an agar plate and a fungal spore suspension (Aspergillus niger, Chaetomium globosum, Paecilomyces variotii, Penicillium funiculosum and Trichoderma longibrachiatum) is added. As a reference, malt-extract agar is embedded instead of a specimen in the agar plate. The plates are inoculated for 21 days. The specimens are laying on agar and have direct contact to water.
Previous studies showed that mould fungi were the first colonizers on WPC material after three months of outdoor exposure (Plaschkies and Scheiding 2014). Ibach et al. (2013) compared decay of WPC from outdoor exposure and in the laboratory. They found mould and algae as the first colonizers. Ibach (2010) also mentioned that the effects of mould fungi are difficult to stop without periodic washing with dilute bleach solution. Lie et al. (2019) compared laboratory screening tests and outdoor performance of exterior wooden claddings. They used agar plate tests and water uptake tests as laboratory methods. The authors investigated various inoculation methods and incubation temperatures. They did not find any significant correlation between the agar test and the outdoor test, but they established significant correlations between the water uptake test and the outdoor test, namely between the water uptake of the specimens and the mould rating of the same specimens after 126 days of outdoor exposure. Scheiding (2007) pointed out that there is a lack of an explicit standard for testing the resistance to mould fungi for wood-based materials including WFIB. Kumar et al. (2016) used octadecyltrichlorosilane for hydrophobic surface treatment of wood fibers to reduce the susceptibility for microorganisms. According to EN ISO 846 (2018), it improved the effectiveness towards mould significantly. Hundhausen et al. (2013) identified the accuracy of the visual assessment as strongly dependent on the evaluator, the type of rating scale and the standard used. They developed a procedure that enabled objective determination of mould growth by using the public domain software ImageJ.
The aim of this study was to compare two standard methods most commonly used for testing the mould resistance of wood-based materials in Europe and to figure out whether the corresponding results correlate. Therefore, two very different types of wood-based materials were compared, i.e. wood polymer composites (WPC) and wood fiber insulation boards (WFIB). Solid wood and pure polymers were tested as references. Mould resistance tests were performed according to BS 3900—Part G6 (1989) and ISO 16869 (2008). It was hypothesized that hardwood containing materials are more susceptible to mould growth compared to softwood containing products due to a higher hemicellulose content and that the mould resistance of WPC decreases with rising wood content.
2 Materials and methods
2.1 Materials
Different types of materials, wood (Scots pine sapwood, beech, black locust purchased from Lower Saxony State Forests) and polymer references (polypropylene from Sabic (Saudi Basic Industries Corporation, Riyadh, Saudi Arabia) and polyethylene from Braskem (Sao Paulo, Brazil)), wood-polymer-composites (WPC) and wood fiber insulation boards (WFIB) were used in this study. For both tests, specimens of the references and WPC had a thickness of 4 mm while the specimens of the WFIB had a thickness of 36 mm. For the tests according to BS 3900-G6 (1989), the specimens were 30 mm x 20 mm with a 2 mm bore-hole drilled 4 mm from the mid-point of the 20 mm side of the references and the WPC specimens. The WFIB specimens did not exhibit a hole. Specimens used for tests according to ISO 16869 (2008) were 20 mm x 20 mm. All test specimens were conditioned at 20 ± 2 °C and 65 ± 10% relative humidity (RH) until constant mass. The number of replicates for each test and material was five references, five WPC specimens, and six WFIB specimens. For WFIB specimens, the higher number of replicates was chosen because two boards per variation were produced and three specimens per board were analyzed.
2.1.1 Production of wood-polymer composites (WPC)
WPC produced in an extrusion (EX), injection molding (IM) and compression molding (CM) process had different shapes; some were solid boards, and some were hollow-chamber profiles. They were partly produced industrially by different industrial partners, partly in laboratory processes conducted by “Süddeutsches Kunststoff-Zentrum (SKZ)” in Würzburg, Germany (WPC 1–3) and partly in cooperation with the Institute of Polymer Materials and Polymer Technology (PuK) at the TU Clausthal, Germany (WPC 4–9). Specimens of industrially produced WPC decking were cut from the inner layer of the material and had accordingly a non-sealed surface with exposed wood particles. Specimens of WPC 1 and 2 were cut from the lateral surface area of the extruded rectangular hollow-chamber profiles. The resulting specimens had a smooth top side and a rough bottom side. The compression molded WPC 3 as well as the injection molded WPC formulations 4–9 had smooth surfaces on both sides of the specimens. Details about the wood species, polymer matrix, and pre-weathering are summarized in Table 1.
Table 1
Wood-polymer composites (WPC), wood and polymer references, wood species, wood percentages, manufacturing method and density
Material | Polymer matrix | Wood species | Wood percentage (%) | Manufacturing method | Density (kg/m³) |
|---|---|---|---|---|---|
Scots pine sapwood | – |
Pinus sylvestris
| 100 | 513 | |
Beech | – |
Fagus sylvatica
| 100 | 667 | |
Black locust | – |
Robinia pseudoacacia
| 100 | 689 | |
Polypropylene | – |
–
| 0 | IM1 | 883 |
Polyethylene | – |
–
| 0 | IM | 951 |
WPC 1 | Polypropylene |
Softwood
5
| 60 | EX2 | 937 |
WPC 2 | Polypropylene |
Softwood
| 70 | EX | 1112 |
WPC 3 (plus biocide4) | Polypropylene |
Softwood
| 60 | CM3 | 1076 |
WPC—Industrial 1 | Polypropylene | n.a. | 60 | 1120 | |
WPC—Industrial 2 | Polyvinyl chloride | n.a. | 50 | 1314 | |
WPC—Industrial 3 | Polyethylene | n.a. | 75 | 1235 | |
WPC—Industrial 4 | Polypropylene | Pulp | 50 | 1143 | |
WPC—Industrial 5 | Polyvinyl chloride | n.a. | 50 | EX | 1337 |
WPC-4-poplar | Polypropylene |
Populus spp.
| 60 | IM | 1096 |
WPC-5-willow | Polypropylene |
Salix spp.
| 60 | IM | 1084 |
WPC-6-spruce | Polypropylene |
Picea abies
| 60 | IM | 1074 |
WPC 7-spruce industrial | Polypropylene |
Softwood
| 60 | IM | 1139 |
WPC 8-young beech | Polypropylene |
Fagus sylvatica
| 60 | IM | 1079 |
WPC 9-old beech | Polypropylene |
Fagus sylvatica
| 60 | IM | 1091 |
WPC—Industrial 1 (4 years o.e.6) | Polypropylene | n.a. | 60 | 1137 | |
WPC—Industrial 2 (6 yearso.e.) | Polyvinyl chloride | n.a. | 50 | 1310 | |
WPC—Industrial 3 (1 yearo.e.) | Polyethylene | n.a. | 75 | EX | 1130 |
2.1.2 Production of wood fiber insulation boards (WFIB)
Specimens were cut from sanded boards produced in a dry process in the Section of Molecular Wood Biotechnology and Technical Mycology, Faculty of Forest Science and Forest Ecology, University of Goettingen. The tested WFIB were made either solely from Norway spruce fibers (Picea abies) or from mixtures of Norway spruce with various hardwood fiber blends in proportions of 20, 50 and 80%. The hardwood fiber blends contained equal proportions of European ash (Fraxinus excelsior), European beech (Fagus sylvatica) and silver birch (Betula pendula). Two types of binders—low temperature curing poly-methylendiphenylisocyanate (PMDI) resin (I-Bond WFI 4370) and bicomponent fibers (Bico-Fibers) - were used to produce either stiff or flexible boards. Further additives used were paraffin wax as hydrophobic agent and ammonium polyphosphate (APP) as flame retardant (Table 2). The percentages of the additives always refer to the dry mass of the fibers.
Table 2
Wood fiber insulation boards (WFIB), respective binders/additives and density
Material | Binders/additives | Density (kg/m³) |
|---|---|---|
20SW1/80HW2 | PMDI3 (5%) | 116,5 |
50SW/50HW | PMDI (5%) | 114,4 |
80SW /20HW | PMDI (5%) | 108,9 |
100 Spruce | PMDI (5%) | 106,5 |
20SW/80HW | PMDI (5%) & APP4 (10%) | 112,2 |
50SW/50HW | PMDI (5%) & APP (10%) | 113,5 |
80SW/20HW | PMDI (5%) & APP (10%) | 106,4 |
100 Spruce | PMDI (5%) & APP (10%) | 104,2 |
20SW/80HW | Bico (7%) | 110,2 |
50SW/50HW | Bico (7%) | 103,8 |
80SW/20HW | Bico (7%) | 98,7 |
100 Spruce | Bico (7%) | 99,3 |
20SW/80HW | PMDI (5%) & paraffin (1%) | 111 |
50SW/50HW | PMDI (5%) & paraffin (1%) | 107,7 |
80SW/20HW | PMDI (5%) & paraffin (1%) | 107,2 |
100 Spruce | PMDI (5%) & paraffin (1%) | 111,7 |
2.2 Mould fungi
To prepare the spore suspension, 5 ml of a wetting agent (0.05% polysorbate dissolution) was added to the cultured (for six to eight weeks) mould fungi, cultivated in agar plates on potato dextrose agar or on malt agar. The different media were selected to provide ideal growth conditions for each fungal species. Afterwards, the spores were harvested with a sterile inoculating loop and all mixed in a beaker. The number of cultures per fungi differed between one and five. To make the standards comparable, a unique spore suspension was used. Differing from the suggested fungi in the standards for all mould resistance tests, the following fungi were used: Aspergillus niger (ATCC 6275), Aspergillus versicolor (IMI 45554), Chaetomium globosum (ATCC 6205), Cladosporium cladosporioides (IMI 178517), Penicillium purpurogenum (IMI178519), Paecilomyces variotii (CBS 628.66), Rhodotorula rubra (main name of strain ID: Rhodotorula mucilaginosa) (NCYC 1659), Stachybotrys atra (IMI 082021), Sydowia polyspora (IMI 269217), Trichurus spiralis (MG 31) and Ulocladium atrum (IMI 79805).
2.2.1 Assessment of mould resistance according to BS 3900—Part G6 (1989)
An incubation chamber (40 × 25 × 25 cm³) was used for the mould resistance tests according to BS 3900-G6 (1989). The conditioned specimens were inoculated via an atomizer with 1 ml of mixed spore suspension. Potential contamination after inoculation was accepted, because the contamination would be with mould fungi again. After inoculation, the specimens were placed in the incubation chamber over a water reservoir with a heating coil. Hooks were plugged through the WPC holes or directly through the WFIB and were hung up on metal ledges (Fig. 1). The temperature of the room, where the incubation chamber was stored, was 23 °C ± 2 ° C. Heating of the water reservoir in the incubation chamber proceeded every 10 h for 2 h throughout the incubation. Temperature and relative humidity were checked every day. Specimens were assessed visually—in the beginning every 2 days, subsequently at larger intervals up to 12 days. Images were taken using a digital microscope VHX 5000 (Keyence, Osaka, Japan) at 50 x magnification. The incubation period was 60 days.
Fig. 1
Incubation chamber used for mould resistance tests according to BS 3900 (1989)
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2.2.2 Assessment of mould resistance according to ISO 16869 (2008)
The WPC specimens were placed in the center of screw jars (diameter: 115 mm, height: 70 mm), which were previously filled with 20 ml of nutrient-salt-agar (2.62 g KH2PO4, 0.2 g Na2HPO4⋅2H2O, 0.7 g MgSO4⋅7H2O, 1.0 g NH4NO3, 15.0 g agar-agar, and 10 ml stock solution of micro-nutrients per 1000 ml aqueous solution). The solution of micro-nutrients contained 0.5 g NaCl, 0.2 g FeSO4⋅7H2O, 0.2 g ZnSO4⋅7H2O, 0.06 g MnSO4⋅H2O per 1000 ml aqueous solution. The jars were autoclaved at 121 °C for 20 min. All specimens were inoculated via an atomizer with 1 ml of the mixed inoculum. All but the WFIB specimens were put on the nutrient-salt-agar, while the WFIB specimens were stamped in the nutrient-salt-agar due to the large thickness. Subsequently, all specimens were covered with 15 ml of nutrient-salt-agar again (Fig. 2). As a reference, malt-agar (30.0 g malt extract, 3.0 g soya peptone, 15.0 g agar-agar, water) was placed in the screw jar replacing the test specimen. All jars were incubated at 22 °C ± 1 °C and 70% RH during 28 days. The deviations in temperature and RH from the standard were defined through the conditions of the culture room. Other deviations from the standard were made to make it comparable to BS 3900.
Fig. 2
Screw jar with an inoculated WFIB-specimen in a mould resistance test according to ISO 16869 (2008)
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Specimens were assessed visually every 2–4 days and images were taken using a digital microscope VHX 5000 (Keyence, Osaka, Japan) at 50x magnification.
2.3 Evaluation of the mould resistance
According to both standards, surface colonization by mould is rated visually. In the chamber test according to BS 3900-G6 (1989), five mould growth classes are defined, while only three classes are distinguished using the agar plate test method ISO 16869 (2008). To allow for a uniform evaluation of both tests, the following five-class assessment scheme was applied in this experiment:
Class 0 = no infestation of the surface.
Class 1 = 1–25% infestation of the surface.
Class 2 = 26–50% infestation of the surface.
Class 3 = 51–75% infestation of the surface.
Class 4 = 76–100% infestation of the surface.
Deviations from the rating scale of the BS 3900-G6 (1989) were made because it includes very small differences between the classes which are not possible to distinguish by a subjective viability control.
2.4 Moisture content measurements
The moisture content (MC) of the specimens was determined after incubation. Therefore, the specimens were cleaned with a soft brush from adhering mould, weighed to the nearest 0.001 g, oven-dried at 103 °C and after cooling down in a desiccator weighed again.
Equation 1: Moisture content (MC).
$$MC=\frac{w-d}{d}*100$$
MC = moisture content, in %.
w = wet mass of the test specimen, in grams.
d = oven dry mass of the test specimen, in grams.
3 Results and discussion
3.1 Mould resistance of wood-polymer composites (WPC)
After seven days, the specimens in the agar plate test were already infected; however, in the chamber test, the first infection was observed after 21 days (Fig. 3). Specimens with higher hardwood content showed a higher degree of colonization by the mould fungi in both tests, which might be attributed to the higher amount of hemicellulose in the hardwoods (Findlay and Savory 1954).
Fig. 3
Classification of mould growth on WPC specimens during the agar plate test (left) and the chamber test (right)
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At the end of the test, none of the PP and PE specimens were infested neither in the chamber test nor in the agar plate test. Solid beech wood specimens were rated in class 2 in the agar plate test and in class 3 in the chamber test: black locust specimens were rated in class 2 and in class 0, respectively. The pine sapwood specimens were rated in class 0 (not infected at all) in the agar plate test, but were rated in class 4 in the chamber test. Lie et al. (2019) also found that pine sapwood was nearly not infected in the agar plate test, but this was not the case in an outdoor test. In the relatively small petri dishes, the emissions of volatile organic compounds (VOCs) might act as an antifungal component.
Mould growth on industrially produced WPC started always earlier in the agar plate test compared to the chamber test. Only on three of the WPC produced in laboratory processes (WPC 1–3), the mould growth started at the same time in both tests.
3.2 Mould resistance of wood fiber insulation boards (WFIB)
In the agar plate test, the mould growth started always earlier and proceeded faster than in the chamber test. After 28 days, none of the WFIB specimens in the chamber test was infected by mould. Therefore, the test was extended to 60 days. The materials with higher hardwood proportions showed more severe mould growth (Fig. 4).
Fig. 4
Mould growth for WFIB during the agar plate test (left side) and the chamber test (right side)
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Unlike Kumar et al. (2016), no positive effect of a hydrophobation additive became visible. Furthermore, there was no effect of the fire retardant additive APP and no significant effect of the binder type (PMDI and bicomponent fibers). The specimens with and without APP and with both types of binder were equally colonized.
Moreover, some of the WFIB specimens were shattered during their placement in the test chamber, because the high porosity of WFIB resulted in brittleness of the specimens.
3.3 Moisture content after incubation
During the agar plate test, the wood references absorbed clearly the highest amount of water. Scots pine sapwood exhibited an average moisture content of 148.3%, beech of 106.7% and black locust of ca. 84.2%. In terms of WPC, higher wood content resulted in higher water absorption (Table 3). ‘WPC—Industrial 4’ (50% wood percentage) and ‘WPC—Industrial 3 old’ (75% wood percentage) absorbed 13.6% and 23.9% of water, respectively. This is due to the higher wood particle content of ‘WPC—Industrial 3 old’.
Table 3
Moisture content of the WPC specimens
Material | Mean moisture content (%) | |
|---|---|---|
Agar plate test | Chamber test | |
Scots pine sapwood | 148.3 | 15.9 |
Beech | 106.7 | 21.1 |
Black locust | 84.2 | 13.5 |
Polypropylene | 0.4 | 0.0 |
Polyethylene | 0.2 | 0.0 |
WPC 1 | 21.1 | 11.2 |
WPC 2 | 19.0 | 14.6 |
WPC 3 (plus biocide) | 15.4 | 12.6 |
WPC—Industrial 1 | 21.0 | 13.2 |
WPC—Industrial 2 | 14.0 | 10.3 |
WPC—Industrial 3 | 21.5 | 14.9 |
WPC—Industrial 4 | 13.6 | 7.9 |
WPC—Industrial 5 | 14.9 | 9.8 |
WPC-4-poplar | 19.0 | 14.2 |
WPC-5-willow | 23.0 | 12.8 |
WPC-6-spruce | 15.7 | 13.6 |
WPC 7-spruce industrial | 18.8 | 13.4 |
WPC 8-young beech | 18.3 | 13.2 |
WPC 9-old beech | 17.0 | 14.1 |
WPC—industrial 1 (4 years o.e.1) | 19.9 | 13.4 |
WPC—industrial 2 (6 years o.e.) | 14.2 | 11.0 |
WPC—industrial 3 (1 year o.e.) | 23.9 | 14.6 |
The moisture content of all specimens in the chamber test was much lower than that of the specimens in the agar plate test. For the wood references, the values were 15.9% for Scots pine sapwood, 21.1% for beech and 13.5% for black locust. As for the agar plate test, WPCs containing more wood had higher moisture content around 14.6% (WPC industrial 3 old) compared to the ones containing less wood with 7.9% moisture content (WPC industrial 4) (Table 3). Clemons (2002) mentioned that the wood flour content, wood particle size, processing methods, and additives influence the moisture absorption of WPC.
High temperatures (over 10 °C are required for growth; 30 °C are favored) and high moisture contents (over 75%) are favorable for mould growth (Schirp and Wolcott 2005; Krause and Schmid 2012; Ibach et al. 2017). Even though many mould species, which are known to grow on wood, have also been isolated from polymers (Schirp et al. 2008), there was no infection of polyethylene and polypropylene specimens in these tests (Figs. 3 and 5 ). This might be explained by insufficient water uptake of the pure polymers (Caulfield et al. 2005) and a lack of additional nutrients.
Fig. 5
Mould growth classes from 0 (left) to 4 (right)
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As for WPC, the agar plate test led to much higher moisture content of WFIB specimens (up to 908.9%) compared to the chamber test (up to 212.6%) (Table 4). This is attributed to the direct contact between the specimens and the agar medium in the agar plate test. In contrast, chamber test specimens took up water only from ambient air in the chamber based on diffusion and condensation only.
Table 4
Moisture content of the WFIB specimen
Material | Additives | Mean moisture content (%) Agar plate test | Mean moisture content (%) Chamber test |
|---|---|---|---|
20SW/80HW | PMDI (5%) | 242.3 | 100.8 |
50SW/50HW | PMDI (5%) | 161.0 | 86.5 |
80SW /20HW | PMDI (5%) | 140.7 | 86.2 |
100 Spruce | PMDI (5%) | 438.1 | 132.0 |
20SW/80HW | PMDI (5%) & APP (10%) | 840.3 | 212.6 |
50SW/50HW | PMDI (5%) & APP (10%) | 881.5 | 205.9 |
80SW/20HW | PMDI (5%) & APP (10%) | 765.8 | 161.7 |
100 Spruce | PMDI (5%) & APP (10%) | 532.9 | 189.6 |
20SW/80HW | Bico (7%) | 722.8 | 111.2 |
50SW/50HW | Bico (7%) | 908.9 | 133.3 |
80SW/20HW | Bico (7%) | 436.9 | 88.4 |
100 Spruce | Bico (7%) | 446.5 | 108.5 |
20SW/80HW | PMDI (5%) & paraffin (1%) | 130.6 | 177.5 |
50SW/50HW | PMDI (5%) & paraffin (1%) | 151.4 | 135.2 |
80SW/20HW | PMDI (5%) & paraffin (1%) | 112.5 | 178.7 |
100 Spruce | PMDI (5%) & paraffin (1%) | 439.9 | 138.6 |
3.4 Comparison of methods
As most of the chamber test specimens were not infected even after 28 days of incubation, ratings were done after 60 days. However, mould growth ratings did not correlate between the two test methods, neither after 28 days nor after 60 days, and neither for WPC nor for WFIB (Fig. 6). The mould fungi grew much faster in the agar plate test than in the chamber test due to the presence of malt extract agar and higher moisture content (Bardage 2004; Schirp et al. 2008).
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There are many implications that can affect mould growth; for instance, the surface structure of the specimens. Gobakken et al. (2010) tested mould growth on paints with different surface structures. They examined six different model paints and found that the mould growth varied with exposure time and type of paint. They suggested that differences in surface structure affect spore attachment and germination, but this did not become evident from their results. They explained that the chemical effect in the coating could be as important as, or more important than, the physical characteristic of the surface.
Moreover, in this study, chemical and/or physical characteristics of the surface could have had an influence on the mould growth, because there were very different surface structures (2.1.1 and 2.1.2) and the chemical ingredients changed a lot between the different variations. The two different additives (APP and paraffin) and binders (PMDI and bicomponent fibers) used for WFIB production influence chemical surface properties.
In addition, the duration of a mould growth experiment plays an important role, since the risk of mould infestation increases with incubation time (Johansson et al. 2012). Hence, future studies shall include long-term outdoor experiments with matched samples to allow for a direct comparison with results from laboratory tests as presented in this study.
Apart from this, different mould growth classification systems are used according to the two standards. In some publications, ‘classes’ are also referred to as ‘index’. Further, Ojanen et al. (2010) report that the defined intervals for the classification vary in different studies. These different assessment systems lead to very poor comparability of the different standards.
3.5 Microscopic evaluation of the mould fungi growth
The microscopic evaluation of the mould growth at 50x magnification turned out unfeasible, because the specimens’ surfaces were very heterogeneous, and thus prone to create shadows and irregularities, which made it impossible to evaluate the infected surfaces.
4 Conclusion
Mould growth ratings obtained with the chamber method and the agar plate method were not well correlated, neither within the group of materials nor across different materials. This was attributed to the much higher moisture content and additional nutrients available for the specimens in the agar plate test compared to those in the chamber test. Thus, for the interpretation of the results, it is very important to know and clearly indicate which standard was used.
Some of the WFIB specimens disintegrated during installation in the test chamber because they were too brittle. For future experiments, it is therefore recommended to use a wire basket or a similar support, when handling WFIB specimens.
Finally, the chamber test appeared preferable over the agar plate method because it represents more realistic exposure conditions for wood-based materials compared to the agar plate test. One more reason that makes the chamber test more comparable to materials used in construction than the agar plate test is that there are no artificially added nutrients. For further validation of the method, field test experiments under different exposure regimes are in preparation.
Acknowledgements
Open Access funding provided by Projekt DEAL. The authors are grateful for financial support in the frame of the projects “WPC-BIO-DEG” (18950N/2) by AIF-IGF (Arbeitsgemeinschaft industrieller Forschungsvereinigungen „Otto von Guericke“ e.V.—Industrielle Gemeinschaftsforschung) and “GerLau” (22015615) by Fachagentur für Nachwachsende Rohstoffe e.V. (FNR).
Compliance with ethical standards
Conflict of Interest
The authors declare no conflicts of interest.
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