No abstract

Surface charring of wood is a one-sided thermal modification process that can be used to create a hydrophobic, durable surface to exterior claddings. Spruce (Picea abies L.) wood samples were charred with a hot plate and several time-temperature combinations while using simultaneous surface compression. Temperature profile, water sorption, cupping after water exposure and density profile were measured. Furthermore, changes in the microstructure and surface functional groups were investigated by scanning electron microscopy and photoacoustic FT-IR spectroscopy. Results show that surface charring notably improves the hydrophobicity measured by contact angle, water floating and dynamic vapour sorption. Increased holding time during charring reduced the sorption but at the same time increased the dimensional instability measured by cupping. The density profile showed a shifting density peak with more severe modification regimes, indicating a more porous surface. The PAS-FTIR showed increased aromaticity of the surface that was also present in the pyrolysis zone beneath the surface in samples modified with longer holding time. Higher modification temperature affected the sorption as well as cupping positively but it is possible similar results can be obtained with lower temperature and longer holding time.

This study investigated several key parameters of deuterium exchange measurements in a dynamic vapour sorption apparatus to optimise the measurement protocol for hydroxyl (OH) group accessibility determination. The impact of changing the sample mass, the deuterium oxide (D2O) vapour exposure time and the rate of change in moisture content (dm dt−1) during the drying steps on the measured OH group accessibility were analysed. A sample mass of more than 10 mg, an exposure to D2O vapour of at least 10 h and a dm dt−1 of 0.0005% min−1 over a 10-min period during the drying steps gave the most reliable results. We also investigated the necessity of adding a method stage that eliminates the effect of inclusion compounds (ICs). The addition of an initial drying and wetting stage enabled the release of entrapped solvents.

In built environments the combustibility of wood is a great concern, which limits the use of wood as a building material due to legislation. The reaction-to-fire properties of wood can be altered with the use of fire-retardant chemicals, and most of the commonly used fire retardants already have a long history of use. However, only limited information is available on the impact of different fire retardants on the adhesion properties of wood. Additionally, comparative studies between chemicals from different groups of fire retardants is scarce. The objective of this study was to investigate and compare the effects of two commonly used fire retardants, sodium silicate (SS) and diammonium phosphate (DAP), on veneer properties, the focus being especially on thermal behavior and adhesion. Thermal properties and combustibility were studied using thermogravimetric analysis (TGA), flame test and calorimetry. Glue bond strength was analyzed with an automated bonding evaluation system (ABES) and the leaching of chemicals was determined according to EN84. Additionally, the surface characteristics of modified veneers were imaged with scanning electron microscopy (SEM). Results revealed notable differences in the thermal properties of SS and DAP, with DAP having better fire-retardant performance in all thermal testing. SS also affected thermal properties and combustibility of modified veneers, but the effect was only moderate compared to DAP. Neither SS or DAP had any significant resistance against leaching but ABES testing showed a notable increase in the glue bond strength of DAP modified veneers.