Background: The genusPleurotusis most exploitable xylotrophic fungi, with valuable biotechnological, medical, and nutritional properties. The relevant features of the representatives of this genus to provide attractive low-cost industrial tools have been reported in numerous studies to resolve the pressure of ecological issues. Additionally, a number ofPleurotusspecies are highly adaptive, do not require any special conditions for growth, and possess specific resistance to contaminating diseases and pests. The unique properties ofPleurotusspecies widely used in many environmental technologies, such as organic solid waste recycling, chemical pollutant degradation, and bioethanol production.Methodology: The literature study encompasses peer-reviewed journals identified by systematic searches of electronic databases such as Google Scholar, NCBI, Springer, ResearchGate, ScienceDirect, and ISI Web of Knowledge. The search scheme was divided into several steps, as described below.Results: In this review, we describe studies examining the biotechnological feasibility ofPleurotusspp. to elucidate the importance of this genus for use in green technology. Here, we review areas of application of the genusPleurotusas a prospective biotechnological tool.Conclusion: The incomplete description of some fungal biochemical pathways emphasises the future research goals for this fungal culture.

Studies on the durability and dimensional stability of a series of hardwoods and softwoods after thermal modification in vegetable oils and in steam atmospheres have been performed. Mass loss after exposure to Coniophora puteana (BAM Ebw.15) for 16 weeks was very low for European birch, European aspen, Norway spruce, and Scots pine thermally modified in a linseed oil product with preservative (for 1 hour at 200 oC). Fairly low mass losses were obtained for wood thermally modified in linseed-, tung- and rapeseed oil, and losses were related to the wood species. Low mass loss during rot test was also found for Norway spruce and Scots pine modified in saturated steam at 180 oC. Water absorption of pine and aspen was reduced by the thermal treatments and the extent of reduction was dependent on wood species and thermal modification method. Thermally modified aspen was stable during cycling climate tests, whereas pine showed considerable cracking when modified under superheated steam conditions (Thermo D). At lower modification temperature (180 oC) an increase in mass after modification in rapeseed oil of spruce, aspen and sapwood as well as heartwood of pine was observed, whereas at high temperature (240 oC) a mass loss could be found. Oil absorption in room tempered oil after thermal modification in oil was high for the more permeable aspen and pine (sapwood).

Fire-retardant (FR) treated wood-based panels, used commonly in furniture and construction, need to meet stringent fire safety regulations. This study presents a novel treatment for imparting fire resistance to wood composites by applying separate solutions of phytic acid and sodium silicate onto wood particles before the hot pressing at 160 °C. A scanning electron microscopy-energy dispersive X-ray spectroscopy (SEM-EDX) analysis revealed that phytic acid and sodium silicate were uniformly distributed throughout the wood particles, and the formation of silica gel resulted in the aggregation of elemental silicon. Fourier-transform infrared spectroscopy (FTIR) displayed that phytic acid caused the thermal degradation of hemicelluloses, which led to a brownish outer appearance of the FR-treated composites. Fire performance was assessed using both limiting oxygen index (LOI) and a cone calorimeter. These techniques showed a higher LOI value and a significant reduction in heat-release rate (HRR), total heat release (THR), smoke-production rate (SPR), and total smoke production (TSP). In addition, cone calorimeter and thermogravimetric (TGA) analyses consistently showed increased char residue in treated wood composites. Moreover, internal bond strength (IB) and modulus of elasticity (MOE) of the wood composite were not significantly changed compared with those of the untreated composite. Surprisingly, in the FR-treated composite, the 24 h-thickness swelling, and the water uptake were slightly decreased. Consequently, this new treatment has the potential to increase the fire retardancy of wood composites, such as particleboard, without deteriorating the key mechanical properties.

With thermal modification, changes in properties of wood, such as the presence of VOC and water-soluble carbohydrates, may occur. Thermal modifications under saturated steam conditions (160 °C or 170 °C) and superheated steam conditions (170, 185, and 212 °C) were investigated by analysing the presence of water-soluble 5-(hydroxymethyl)furfural (HMF), furfural, and carbohydrates in heat-treated wood. The influence of thermal modifications on Scots pine, Norway spruce, and silver birch was also studied. Furfurals were analysed using HPLC at 280 nm, while monosaccharides and water-soluble carbohydrates were determined by GC-FID as their acetylated alditiols and, after methanolysis, as their trimethylsilylated methyl-glycosides, respectively. The amount of furfurals was larger in boards thermally modified under saturated steam conditions than those treated under superheated steam conditions. Generally, more of HMF than furfural was found in the thermally modified boards. In process water, in which saturated steam conditions had been used, furfural and only traces of HMF were found. Higher content of water-soluble carbohydrates was found in boards treated in saturated steam rather than in superheated steam. After modification in saturated steam, substantial parts of the water-soluble carbohydrates were due to monosaccharides, but only traces of monosaccharides were found in boards treated under superheated steam conditions.

Guanyl-urea phosphate (GUP) was introduced into furfurylated wood in order to improve fire retardancy. Modified wood was produced via vacuum-pressure impregnation of the GUP–furfuryl alcohol (FA) aqueous solution, which was then polymerized at elevated temperature. The water leaching resistance of the treated wood was tested according to European standard EN 84, while the leached water was analyzed using ultra-performance liquid chromatography (UPLC) and inductively coupled plasma–sector field mass spectrometry (ICP-SFMS). This new type of furfurylated wood was further characterized in the laboratory by evaluating its morphology and elemental composition using optical microscopy and electron microscopy coupled with energy-dispersive X-ray spectrometry (SEM-EDX). The chemical functionality was detected using infrared spectroscopy (FTIR), and the fire resistance was tested using cone calorimetry. The dimensional stability was evaluated in wet–dry soaking cycle tests, along with the mechanical properties, such as the Brinell hardness and bending strength. The fire retardancy of the modified furfurylated wood indicated that the flammability of wood can be depressed to some extent by introducing GUP. This was reflected in an observed reduction in heat release rate (HRR₂) from 454.8 to 264.9 kW/m², without a reduction in the material properties. In addition, this leaching-resistant furfurylated wood exhibited higher fire retardancy compared to conventional furfurylated wood. A potential method for producing fire-retardant treated furfurylated wood stable to water exposure has been suggested.