Feasibility of Manufacturing Strand-Based Wood Composite Treated with β-Cyclodextrin–Boric Acid for Fungal Decay Resistance

The feasibility of using β-cyclodextrin (βCD) as an eco-friendly carrier of boric acid for the protection of strand-based wood composites against decay fungi was evaluated. The formation of a βCD–boric acid (βCD–B) complex was confirmed by the appearance of the boron–oxygen bond by using attenuated total reflection–Fourier transform infrared spectroscopy. Chemical shifts of around 6.25 and 1.41 ppm were also observed in 1H Nuclear Magnetic Resonance (NMR) and 11B NMR spectra, respectively. The βCD–B preservatives at two levels (5 and 10 wt.%) were uniformly blended with southern pine strands that were subsequently sprayed with polymeric methylene diphenyl diisocyanate (pMDI) resin. The blended strands were formed into a loose mat by hand and consolidated into 25 × 254 × 12 mm oriented strand boards (OSB) using a hot-press. The OSB panels were cut to end-matched internal bonding (IB) strength and fungal decay resistance test specimens. The vertical density profiles (VDPs) of the IB specimens were measured using an X-ray based density profiler and the specimens with statistically similar VDPs were selected for the IB and decay tests. The IB strength of the treated specimens was lower than the control specimens but they were above the required IB strength of heavy-duty load-bearing boards for use in humid conditions, specified in the BS EN 300:2006 standard. The reduced IB of preservative-treated OSB boards could be explained by the destabilized resin upon the addition of the βCD–B complex, as indicated by the differential scanning calorimetry (DSC) results. The resistance of the OSB panels against two brown-rot fungi (i.e., G. trabeum or P. placenta) was evaluated before and after accelerated leaching cycles. The treated OSBs exposed to the fungi showed an average mass loss of lower than 3% before leaching, while the untreated OSBs had 49 and 35% mass losses due to decay by G. trabeum or P. placenta, respectively. However, upon the leaching, the treatment provided protection only against G. trabeum to a certain degree (average mass loss of 15%). The experimental results suggest that protection efficacy against decay fungi after leaching, as well as the adhesion of the OSB strands, can be improved by increasing the amount of pMDI resin.


Introduction
The protection of wood composites by various biocides has been practiced since the end of the last century [1]. Most of the conventionally used preservatives are either heavy metal based

Preparation of βCD-B Complex
The βCD-B complex was prepared by mixing βCD (Acros Organics, New Jersey, USA) with boric acid (Fisher Chemical, New Jersey, US) at a molar ratio of 1:7 and refluxing the mixture in toluene (Fisher Chemical, New Jersey, USA) in a Dean-Stark apparatus for 18 h [13] (Figure 1). The residual toluene was removed in a rotary evaporator and the resultant mixture was kept in a desiccator prior to analysis. The physical mixture of βCD and boric acid was obtained by homogenizing the two powders using the same molar ratio.

Attenuated Total Reflection-Fourier Transform Infrared Spectroscopy (ATR-FTIR)
The formation of the βCD-B complex was confirmed by a PerkinElmer Spectrum Two FTIR spectrometer equipped with a universal ATR (PerkinElmer, Waltham, MA, USA). Three replicates of ATR-FTIR spectra were obtained for every sample in the spectral range of 4000 to 400 cm −1 at a resolution of 4 cm −1 . All the spectra were baseline-corrected interactively using Spectrum ® Quant software (PerkinElmer, Waltham, MA, USA).

Nuclear Magnetic Resonance Analysis
The βCD-B complex was further confirmed by 1 H NMR and 11 B NMR using a Bruker AVANCE III spectrometer (Billerica, MA, USA) operated at 500 MHz. DMSO-d6 was used as the solvent and tetramethylsilane (TMS) was used as an internal reference for 1 H NMR. The solutions were transferred into 5 mm NMR tubes to a total sample height of 4 cm. The probe temperature was maintained at 25 °C. Chemical shifts were expressed in parts per million downfield from the signal (0 ppm) of TMS.

Differential Scanning Calorimetry (DSC) Analysis
DSC (SDT Q600, TA instruments, New Castle, DE, USA) was used to study the interactions between pMDI resin, the βCD-B complex and southern pine wood flour. Samples (10 ± 0.5 mg) of pMDI resin, wood, βCD-B and a physical mixture of any two or all three components at an equal weight ratio was weighed into aluminum pans and sealed with a pierced lid. The measurements were performed under a nitrogen atmosphere with a flow rate of 100 mL/min and all the samples were subjected to the same thermal history with the following protocol. First, the samples were heated from 26 to 120 °C at a heating rate of 10 °C/min and cooled to room temperature. This process was repeated two times to erase the thermal history and reduce variations in data interpretation. Second, the samples were heated from 26 to 250 °C at a heating rate of 10 °C/min to determine their thermal properties. Two replicate runs were performed for each sample.

Preparation of Oriented Strand Board (OSB)
Test panels were made under lab conditions ( Figure 2). First, southern pine wood strands (Norbord Inc, Guntown, MS, USA) were dried to 6% moisture content and were mixed with 0%, 5% or 10% preservative (based on the oven-dried weight of strands), corresponding to boric acid

Attenuated Total Reflection-Fourier Transform Infrared Spectroscopy (ATR-FTIR)
The formation of the βCD-B complex was confirmed by a PerkinElmer Spectrum Two FTIR spectrometer equipped with a universal ATR (PerkinElmer, Waltham, MA, USA). Three replicates of ATR-FTIR spectra were obtained for every sample in the spectral range of 4000 to 400 cm −1 at a resolution of 4 cm −1 . All the spectra were baseline-corrected interactively using Spectrum ® Quant software (PerkinElmer, Waltham, MA, USA).

Nuclear Magnetic Resonance Analysis
The βCD-B complex was further confirmed by 1 H NMR and 11 B NMR using a Bruker AVANCE III spectrometer (Billerica, MA, USA) operated at 500 MHz. DMSO-d6 was used as the solvent and tetramethylsilane (TMS) was used as an internal reference for 1 H NMR. The solutions were transferred into 5 mm NMR tubes to a total sample height of 4 cm. The probe temperature was maintained at 25 • C. Chemical shifts were expressed in parts per million downfield from the signal (0 ppm) of TMS.

Differential Scanning Calorimetry (DSC) Analysis
DSC (SDT Q600, TA instruments, New Castle, DE, USA) was used to study the interactions between pMDI resin, the βCD-B complex and southern pine wood flour. Samples (10 ± 0.5 mg) of pMDI resin, wood, βCD-B and a physical mixture of any two or all three components at an equal weight ratio was weighed into aluminum pans and sealed with a pierced lid. The measurements were performed under a nitrogen atmosphere with a flow rate of 100 mL/min and all the samples were subjected to the same thermal history with the following protocol. First, the samples were heated from 26 to 120 • C at a heating rate of 10 • C/min and cooled to room temperature. This process was repeated two times to erase the thermal history and reduce variations in data interpretation. Second, the samples were heated from 26 to 250 • C at a heating rate of 10 • C/min to determine their thermal properties. Two replicate runs were performed for each sample.

Preparation of Oriented Strand Board (OSB)
Test panels were made under lab conditions ( Figure 2). First, southern pine wood strands (Norbord Inc, Guntown, MS, USA) were dried to 6% moisture content and were mixed with 0%, 5% or 10% preservative (based on the oven-dried weight of strands), corresponding to boric acid equivalent (BAE) levels of 0%, 1.5% and 3.0%, respectively, in a rotary laboratory-type blender at a rotating speed of 20 rpm for 2 min. Subsequently, 0.04 g polymeric diphenylmethane diisocyanate (pMDI) resin Polymers 2020, 12, 274 4 of 13 (Huntsmen, Conroe, TX, USA) per g of wood was sprayed into the rotating drum using a spray gun with a nozzle size of 1.0 mm, followed by another 3 min of blending. The strands were transferred into a 254 × 254 mm mold randomly by hand. The formed mats were pressed at 176 ± 3 • C for 200 s to a target thickness of 11.7 mm. The panels were conditioned at 21 • C and 64% relative humidity (RH) before testing.
Polymers 2020, 12, x FOR PEER REVIEW 4 of 14 equivalent (BAE) levels of 0%, 1.5% and 3.0%, respectively, in a rotary laboratory-type blender at a rotating speed of 20 rpm for 2 min. Subsequently, 0.04 g polymeric diphenylmethane diisocyanate (pMDI) resin (Huntsmen, Conroe, TX, USA) per g of wood was sprayed into the rotating drum using a spray gun with a nozzle size of 1.0 mm, followed by another 3 min of blending. The strands were transferred into a 254 × 254 mm mold randomly by hand. The formed mats were pressed at 176 ± 3 °C for 200 s to a target thickness of 11.7 mm. The panels were conditioned at 21 °C and 64% relative humidity (RH) before testing.

Internal Bond Strength and Fungal Resistance of OSB
Prior to examining the thickness-wise cohesion and fungal decay resistance of the panel, the vertical density profiles (VDPs) of the samples were measured using a QMS Density profiler (model QDP-01 X, Quintek Measurement Systems, Inc. Oak Ridge, TN, USA). Twenty-four internal bonding (IB) test samples (51 × 51 × 11.7 mm) of each treatment were weighed to a precision of 0.01 g. Three end-matched fungal decay test samples (14 × 14 × 11.7 mm) were cut from a 14 mm-wide strip next to each IB sample. The VDPs data were normalized using linear interpolation in accordance with the sample thickness, and the averaged VDPs of each treatment were reported. The samples with a squared residual (r 2 ) greater than 0.56 were used for internal bonding tests.
The IB strength of the samples was examined as described in the ASTM D1037-12 standard [20]. Both wide faces of the samples were attached to the aluminum alloy holding blocks using a hot melt glue (Type 34614C, Applied Adhesives, MN, USA). A tensile loading perpendicular to sample surfaces was applied at a rate of 0.935 mm/min using a universal testing instrument (Instron 4204, Instron Corporation, Norwood, MA, USA). The IB strength was calculated using the following Equation IB strength (MPa) = maximum load (N) length (mm) × width (mm) (1) Before exposure to fungi, the long-term performance of βCD-B-treated OSB samples was tested following the leaching procedures described in AWPA Standard E11-16 [21]. Briefly, half of the fungal decay test samples were placed into beakers and weighed down to prevent floating. A total of 240 mL of deionized water was added to each beaker, and the beakers were placed at room temperature on an orbital shaker rotating at a speed of 100 rpm. After 6, 24, 48 h, and thereafter at 48 h intervals, the leachate was removed from the beakers, and replaced with 100 mL fresh deionized water. The leaching process was performed for a total of 14 days.
The effect of the βCD-B complex on the decay resistance of the treated OSB samples was evaluated following AWPA Standard E10 [22]. Both unleached and leached specimens were sterilized by dipping the samples in 70% ethanol for 10 s and drying in a laminar flow cabinet, followed by the exposure of samples to one of two brown-rot fungi, Gloeophyllum trabeum (ATCC isolate 11539) and Postia placenta (ATCC 11538) for eight weeks. The mass loss was calculated according to the following Equation

Internal Bond Strength and Fungal Resistance of OSB
Prior to examining the thickness-wise cohesion and fungal decay resistance of the panel, the vertical density profiles (VDPs) of the samples were measured using a QMS Density profiler (model QDP-01 X, Quintek Measurement Systems, Inc. Oak Ridge, TN, USA). Twenty-four internal bonding (IB) test samples (51 × 51 × 11.7 mm) of each treatment were weighed to a precision of 0.01 g. Three end-matched fungal decay test samples (14 × 14 × 11.7 mm) were cut from a 14 mm-wide strip next to each IB sample. The VDPs data were normalized using linear interpolation in accordance with the sample thickness, and the averaged VDPs of each treatment were reported. The samples with a squared residual (r 2 ) greater than 0.56 were used for internal bonding tests.
The IB strength of the samples was examined as described in the ASTM D1037-12 standard [20]. Both wide faces of the samples were attached to the aluminum alloy holding blocks using a hot melt glue (Type 34614C, Applied Adhesives, MN, USA). A tensile loading perpendicular to sample surfaces was applied at a rate of 0.935 mm/min using a universal testing instrument (Instron 4204, Instron Corporation, Norwood, MA, USA). The IB strength was calculated using the following Equation Before exposure to fungi, the long-term performance of βCD-B-treated OSB samples was tested following the leaching procedures described in AWPA Standard E11-16 [21]. Briefly, half of the fungal decay test samples were placed into beakers and weighed down to prevent floating. A total of 240 mL of deionized water was added to each beaker, and the beakers were placed at room temperature on an orbital shaker rotating at a speed of 100 rpm. After 6, 24, 48 h, and thereafter at 48 h intervals, the leachate was removed from the beakers, and replaced with 100 mL fresh deionized water. The leaching process was performed for a total of 14 days.
The effect of the βCD-B complex on the decay resistance of the treated OSB samples was evaluated following AWPA Standard E10 [22]. Both unleached and leached specimens were sterilized by dipping the samples in 70% ethanol for 10 s and drying in a laminar flow cabinet, followed by the exposure of samples to one of two brown-rot fungi, Gloeophyllum trabeum (ATCC isolate 11539) and Postia placenta (ATCC 11538) for eight weeks. The mass loss was calculated according to the following Equation where m and m exp. are the oven-dried mass of untreated or treated OSB cubes before and after exposure to fungi, respectively.

Statistical Analysis
Statistical analysis was performed using Statistical Analysis System software (SAS version 9.4, SAS Institute, Cary, NC). The data were compared using a one-way analysis of variance (ANOVA) followed by post-hoc Fisher's Least Significant Difference (p < 0.05) to identify the effects of preservative levels on the IB, average densities and mass loss of the panels after exposure to fungi.

Formation of βCD-B Complex
The formation of the βCD-B complex was evident by changes in the IR spectra of the complex, as compared to the spectra of the individual components and physical mixture ( Figure 3). The FTIR spectrum of boric acid exhibits absorption bands at 3193 and 1409 cm −1 due to the stretching of O-H and asymmetric stretching of the B-O bond, respectively [23]. In the spectrum of the βCD, a sharp absorption band at 3308 cm −1 and an intense peak at 1078 cm −1 due to stretching of the O-H and C-O bond, respectively, were seen. The 2924 cm −1 peak corresponds to C-H stretching while the 1367 cm −1 peak can be attributed to scissoring of the C-H group [24]. Upon reaction with boric acid, the O-H band in the complex shifted to a lower frequency (~3209 cm −1 ) and became narrower, as compared to those of the physical mixture (~3220 cm −1 ) and pure βCD (~3308 cm −1 ). Also, the intensity of O-H stretching at 1645 cm −1 was greatly reduced in the βCD-B complex. These observations suggest that a fraction of the O-H groups in βCD are substituted by boric acid, as shown in Figure 3. Moreover, the C-H stretching (~2924 cm −1 ) in the βCD-B complex exhibited a lower intensity and shifted to a lower frequency, which possibly resulted from an altered environment around these bonds upon complexation. These results were also supported by the appearance of new borate ester B (OR) 3 peaks at 1473, 805, 728 cm −1 . Therefore, the formation of the βCD-B complex was indicated by the changes in OH groups and the formation of new peaks attributed to borate ester [25].  The 1 H NMR results of boric acid, βCD, and βCD-B complex are shown in Figure 4a. A new peak at 6.25 ppm was observed in the 1 H NMR spectrum of βCD-B, as compared to that of the neat βCD. Also, the decreased intensities in the peaks of H-3 and H-6 relative to the peak of H-2 in βCD-B suggest that borate esters are replacing the OH groups in βCD. According to the NMR results, the OH groups in boric acid may either attach at the OH sites corresponding to the H-2, H-3 or H-6 peaks in cyclodextrins [26].
The complexation between βCD and boric acid was also confirmed by 11 B NMR. Figure 4b shows the normalized 11 B NMR spectra of boric acid, βCD-B complex and the physical mixtures. Only one peak (at around 20 ppm) was observed in the 11 B NMR spectra of boric acid. Conversely, there was a new peak at 1.41 ppm in the 11 B NMR spectrum of the βCD-B complex, which was assigned to the B-O-C bond containing residual-OH groups from boric acid [27]. A small peak at 1.38 ppm was also observed in the βCD&B physical mixture due to the tendency of poly-condensation between boric acid and polyols and the prevention of hydrolysis by using DMSO-d6 as a solvent. The 1 H NMR results of boric acid, βCD, and βCD-B complex are shown in Figure 4a. A new peak at 6.25 ppm was observed in the 1 H NMR spectrum of βCD-B, as compared to that of the neat βCD. Also, the decreased intensities in the peaks of H-3 and H-6 relative to the peak of H-2 in βCD-B suggest that borate esters are replacing the OH groups in βCD. According to the NMR results, the OH groups in boric acid may either attach at the OH sites corresponding to the H-2, H-3 or H-6 peaks in cyclodextrins [26].  The DSC curves of pMDI resin, wood, βCD, βCD-B complex, and the physical mixture of any two, or all three, of the components at equal weights are shown in Figure 5. An exothermic peak was  The complexation between βCD and boric acid was also confirmed by 11 B NMR. Figure 4b shows the normalized 11 B NMR spectra of boric acid, βCD-B complex and the physical mixtures. Only one peak (at around 20 ppm) was observed in the 11 B NMR spectra of boric acid. Conversely, there was a new peak at 1.41 ppm in the 11 B NMR spectrum of the βCD-B complex, which was assigned to the B-O-C bond containing residual-OH groups from boric acid [27]. A small peak at 1.38 ppm was also observed in the βCD&B physical mixture due to the tendency of poly-condensation between boric acid and polyols and the prevention of hydrolysis by using DMSO-d6 as a solvent. The DSC curves of pMDI resin, wood, βCD, βCD-B complex, and the physical mixture of any two, or all three, of the components at equal weights are shown in Figure 5. An exothermic peak was observed in the βCD-B complex ( Figure 5, black curve; compare to the pink curve below). This peak could be attributed to the decomposition of the βCD-B complex, and similar results with a higher decomposition temperature have been reported when starch was esterified by boric acid [28]. Moreover, this peak centered at 183 • C in the βCD-B complex shifted to the lower temperature of 158 • C in the presence of the pMDI resin and shifted slightly further to 156 • C when blended with wood. This fact could be related to the high reactivity rate of decomposed boron towards isocyanate-containing resins [29]. The decreased exothermic temperature in the mixture of resin, wood and preservatives indicates that the addition of βCD-B complex possibly lowered the temperature required to initiate the curing reaction of resin, as boron compounds have been used to catalyze the polymerization in isocyanate-based resin systems [11,30,31] Polymers 2020, 12, x FOR PEER REVIEW 8 of 14 observed in the βCD-B complex ( Figure 5, black curve; compare to the pink curve below). This peak could be attributed to the decomposition of the βCD-B complex, and similar results with a higher decomposition temperature have been reported when starch was esterified by boric acid [28]. Moreover, this peak centered at 183 °C in the βCD-B complex shifted to the lower temperature of 158 °C in the presence of the pMDI resin and shifted slightly further to 156 °C when blended with wood. This fact could be related to the high reactivity rate of decomposed boron towards isocyanatecontaining resins [29]. The decreased exothermic temperature in the mixture of resin, wood and preservatives indicates that the addition of βCD-B complex possibly lowered the temperature required to initiate the curing reaction of resin, as boron compounds have been used to catalyze the polymerization in isocyanate-based resin systems [11,30,31]

Vertical Density Profile (VDP) and Internal Bonding of the Panel
The average VDPs, normalized based on the thicknesses of the IB test specimens of each panel, are presented in Figure 6a, which are characterized by high-density near the panel surfaces and lowdensity at the panel cores. VDPs are determined by hot press manufacturing parameters such as the moisture distribution in the mat, pressing schedules, and platen temperatures [32]. The average densities of the panels near the surface regions (10%-20% and 80%-90% of the normalized thicknesses) and at core regions (45%-55% of the normalized thicknesses) are shown in Table 1. The average densities of the surface regions were significantly higher than the core regions for all three treatments. The average densities of the surface regions #1 and #2 at 5% preservative treatment increased by 7% and 9%, respectively, while the densities of the core regions were not significantly affected as compared to those of the control. The addition of 10% preservative increased the densities of the surface regions #1 and #2 by 16% and 19%, respectively, while it increased the core density by 8% compared to the control. These results indicate that the preservative addition densified the surface layers more than the core layers and affected compaction throughout the thicknesses of the treated panels. As discussed in the previous section, the boron-based preservative particles possibly lowered the curing temperature of the pMDI resin and accelerated densification near the panel surfaces. Such

Vertical Density Profile (VDP) and Internal Bonding of the Panel
The average VDPs, normalized based on the thicknesses of the IB test specimens of each panel, are presented in Figure 6a, which are characterized by high-density near the panel surfaces and low-density at the panel cores. VDPs are determined by hot press manufacturing parameters such as the moisture distribution in the mat, pressing schedules, and platen temperatures [32]. The average densities of the panels near the surface regions (10%-20% and 80%-90% of the normalized thicknesses) and at core regions (45%-55% of the normalized thicknesses) are shown in Table 1. The average densities of the Polymers 2020, 12, 274 8 of 13 surface regions were significantly higher than the core regions for all three treatments. The average densities of the surface regions #1 and #2 at 5% preservative treatment increased by 7% and 9%, respectively, while the densities of the core regions were not significantly affected as compared to those of the control. The addition of 10% preservative increased the densities of the surface regions #1 and #2 by 16% and 19%, respectively, while it increased the core density by 8% compared to the control. These results indicate that the preservative addition densified the surface layers more than the core layers and affected compaction throughout the thicknesses of the treated panels. As discussed in the previous section, the boron-based preservative particles possibly lowered the curing temperature of the pMDI resin and accelerated densification near the panel surfaces. Such densification then would affect the mass and heat movements toward the panel cores and decrease their compactness ratios from the control [33,34].
Polymers 2020, 12, x FOR PEER REVIEW 9 of 14 densification then would affect the mass and heat movements toward the panel cores and decrease their compactness ratios from the control [33,34]. The average IB strength values of the panel as a function of the preservative level are presented in Figure 6b. The addition of preservatives significantly decreased the cohesion strength of the panels, mainly by reducing the compaction ratios of the panel cores, as discussed earlier. Additionally, due to the low water solubility of the βCD-B complex, most of the compounds would sit in a powder form on the surface of the wood during hot pressing, resulting in a lager surface area of solids within the mat and a lower bonding efficiency of the resin [11]. Meanwhile, a significant increase in IB strength was observed when the preservative loading was increased from 5% to 10%. The increased amount of boric acid in the βCD-B complex may have acted as a crosslinking agent that improved the bonding strength of the pMDI resin in the presence of steam [29,35]. Further investigation on the interactions between βCD-B, pMDI, and wood in the presence of water is needed. Although the addition of the βCD-B complex overall significantly reduced the internal bonding of the panel, their IB was above the BS EN 300 standard for load-bearing boards for use in humid conditions (Type OSB/3) [36].

Decay Resistance of βCD-B Complex Against Brown-Rot Fungi
The fungal resistance of southern pine OSB panels treated with βCD-B at levels of 0%, 5% and 10% was tested against G. trabeum and P. placenta for an incubation time of eight weeks. Figure 7a shows the unexposed control and decayed OSB samples. The unleached, treated OSB cubes showed limited decay as compared to the extensively colonized control and treated, leached samples. The mass loss of OSB samples is shown in Figure 7b. The average percent mass loss caused by G. trabeum in the untreated control group (both unleached and leached) showed a mass loss greater than 45%, indicating a high activity of the fungus used for testing. In comparison, the mass loss of unleached OSB treated with 5% βCD-B complex was significantly decreased to approximately 3% (p < 0.05), which is not significantly different from the mass loss of OSB samples containing 10% βCD-B complex, as both treatment levels were above the preservative threshold of 1% (BAE) [37]. This  Note: Means followed by the same letter are not significantly different (LSD, p < 0.05). * Data from a submitted manuscript [16].
The average IB strength values of the panel as a function of the preservative level are presented in Figure 6b. The addition of preservatives significantly decreased the cohesion strength of the panels, mainly by reducing the compaction ratios of the panel cores, as discussed earlier. Additionally, due to the low water solubility of the βCD-B complex, most of the compounds would sit in a powder form on the surface of the wood during hot pressing, resulting in a lager surface area of solids within the mat and a lower bonding efficiency of the resin [11]. Meanwhile, a significant increase in IB strength was observed when the preservative loading was increased from 5% to 10%. The increased amount of boric acid in the βCD-B complex may have acted as a crosslinking agent that improved the bonding strength of the pMDI resin in the presence of steam [29,35]. Further investigation on the interactions between βCD-B, pMDI, and wood in the presence of water is needed. Although the addition of the βCD-B complex overall significantly reduced the internal bonding of the panel, their IB was above the BS EN 300 standard for load-bearing boards for use in humid conditions (Type OSB/3) [36].

Decay Resistance of βCD-B Complex Against Brown-Rot Fungi
The fungal resistance of southern pine OSB panels treated with βCD-B at levels of 0%, 5% and 10% was tested against G. trabeum and P. placenta for an incubation time of eight weeks. Figure 7a shows the unexposed control and decayed OSB samples. The unleached, treated OSB cubes showed limited decay as compared to the extensively colonized control and treated, leached samples. The mass loss of OSB samples is shown in Figure 7b. The average percent mass loss caused by G. trabeum in the untreated control group (both unleached and leached) showed a mass loss greater than 45%, indicating a high activity of the fungus used for testing. In comparison, the mass loss of unleached OSB treated with 5% βCD-B complex was significantly decreased to approximately 3% (p < 0.05), which is not significantly different from the mass loss of OSB samples containing 10% βCD-B complex, as both treatment levels were above the preservative threshold of 1% (BAE) [37]. This observation also indicates that the bioavailability of boron in the βCD-B complex was not affected by encapsulation. In the case of leached samples, the mass losses of 5% and 10% βCD-B complex treatments were not significantly different (~15%, p < 0.05), but still significantly lower than the mass loss of control groups (50%-60%, p < 0.05). These results indicate that the βCD-B complex or boric acid are leached from the samples, resulting in reduced resistance against the fungus.
Polymers 2020, 12, x FOR PEER REVIEW 10 of 14 observation also indicates that the bioavailability of boron in the βCD-B complex was not affected by encapsulation. In the case of leached samples, the mass losses of 5% and 10% βCD-B complex treatments were not significantly different (~15%, p < 0.05), but still significantly lower than the mass loss of control groups (50%-60%, p < 0.05). These results indicate that the βCD-B complex or boric acid are leached from the samples, resulting in reduced resistance against the fungus. Unleached, treated samples exposed to P. placenta also showed low mass losses, indicating that P. placenta and G. trabeum might have a similar BAE threshold, as reported by Freitag and Morrell [38]. However, the leached samples treated with both preservative levels (at 5% and 10% βCD-B) showed a significantly higher mass loss than those exposed to G. trabeum (p < 0.05). In this study, the mass loss differences in the leached samples in these two fungi could result from the variations in the panels selected for the soil block test, as the decay test specimens for G. trabeum and P. placenta were (a) Unleached, treated samples exposed to P. placenta also showed low mass losses, indicating that P. placenta and G. trabeum might have a similar BAE threshold, as reported by Freitag and Morrell [38].
However, the leached samples treated with both preservative levels (at 5% and 10% βCD-B) showed a significantly higher mass loss than those exposed to G. trabeum (p < 0.05). In this study, the mass loss differences in the leached samples in these two fungi could result from the variations in the panels selected for the soil block test, as the decay test specimens for G. trabeum and P. placenta were selected from different panels. Another reason could be related to more delamination of specimens during P. placenta exposure under warm and humid conditions, which could lead to high leaching rates [39].
The leaching of boric acid in this study, indicated by the increased mass losses of leached samples, likely results from the hydrolysis of boric acid from βCD-B. In this study, βCD-B was obtained by the esterification reaction between boric acid and cyclodextrin. It has been reported that the greater the bulk of the R group in the borate esters (Figure 8), the slower the hydrolysis rate [40,41]. However, the intrinsic low hydrolysis stability of boric acid esters remains [41] because of the empty p-orbital in boron [42]. In other words, three of the hybridized sp2 orbitals form covalent bonds with other atoms, while one unhybridized p-orbital remains unoccupied. The vacant p-orbital imparts the compounds with Lewis acid character and tends to accept unshared electrons from donor species, e.g., water molecules [25]. Therefore, due to the tendency of boron to be attacked by water and the harsh leaching conditions employed in this study, boric acid might be released from the βCD-B complex, consequently compromising the durability of the fungal exposed samples. Bioavailable borate is necessary for wood protection, and permanently immobilized borates would reduce the biological activity of borate complexes [43,44]. Therefore, it might be beneficial to design borate esters with a controlled hydrolysis rate and evaluate their biological performance over time.
Polymers 2020, 12, x FOR PEER REVIEW 11 of 14 selected from different panels. Another reason could be related to more delamination of specimens during P. placenta exposure under warm and humid conditions, which could lead to high leaching rates [39]. The leaching of boric acid in this study, indicated by the increased mass losses of leached samples, likely results from the hydrolysis of boric acid from βCD-B. In this study, βCD-B was obtained by the esterification reaction between boric acid and cyclodextrin. It has been reported that the greater the bulk of the R group in the borate esters (Figure 8), the slower the hydrolysis rate [40,41]. However, the intrinsic low hydrolysis stability of boric acid esters remains [41] because of the empty p-orbital in boron [42]. In other words, three of the hybridized sp2 orbitals form covalent bonds with other atoms, while one unhybridized p-orbital remains unoccupied. The vacant p-orbital imparts the compounds with Lewis acid character and tends to accept unshared electrons from donor species, e.g., water molecules [25]. Therefore, due to the tendency of boron to be attacked by water and the harsh leaching conditions employed in this study, boric acid might be released from the βCD-B complex, consequently compromising the durability of the fungal exposed samples. Bioavailable borate is necessary for wood protection, and permanently immobilized borates would reduce the biological activity of borate complexes [43,44]. Therefore, it might be beneficial to design borate esters with a controlled hydrolysis rate and evaluate their biological performance over time.

Conclusions
The difference between the mass loss of control group and βCD-B-complex-treated OSB indicates the suitability of βCD-B as a potential wood preservative for wood composites' protection. Boric acid can be partially fixed by βCD and the bioavailability of the βCD-B complex is not affected by encapsulation. The internal bond strength of the βCD-B-preservative-treated panel meets the minimum requirement for the European standard for load-bearing boards for use in humid conditions. However, the βCD-B complex is prone to hydrolysis, thus the constructed OSB could only be used where there is a minimum leaching hazard. Future research will continue to focus on improving the leaching performance of βCD-B-complex-treated OSB. The mold resistance and mechanical properties of the treated panels made, implementing the optimized manufacturing parameters, will also be investigated.

Conclusions
The difference between the mass loss of control group and βCD-B-complex-treated OSB indicates the suitability of βCD-B as a potential wood preservative for wood composites' protection. Boric acid can be partially fixed by βCD and the bioavailability of the βCD-B complex is not affected by encapsulation. The internal bond strength of the βCD-B-preservative-treated panel meets the minimum requirement for the European standard for load-bearing boards for use in humid conditions. However, the βCD-B complex is prone to hydrolysis, thus the constructed OSB could only be used where there is a minimum leaching hazard. Future research will continue to focus on improving the leaching performance of βCD-B-complex-treated OSB. The mold resistance and mechanical properties of the treated panels made, implementing the optimized manufacturing parameters, will also be investigated.