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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. Validerad;2023;Nivå 2;2023-05-22 (hanlid);Funder: Slovak Research and Development Agency (APVV-16-0223); VEGA agency (VEGA 1/0678/22); KEGA agency (KEGA 016STU4/2021); Swedish wood industry; OP RDE (CZ.02.1.01/0.0/0.0/16_019/0000803) Biobased fire protection of wood panel for exterior conditions by using phosphorylated lignin from wheat straw Advanced research supporting the forestry and woodprocessing sector’s adaptation to global change and the 4th industrial revolution

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.

In this study, the wood–water interactions in Scots pine sapwood modified with maleic anhydride (MA) and sodium hypophosphite (SHP) was studied in the water-saturated state. The water in wood was studied with low field nuclear magnetic resonance (LFNMR) and the hydrophilicity of cell walls was studied by infrared spectroscopy after deuteration using liquid D2O. The results of LFNMR showed that the spin–spin relaxation (T2) time of cell wall water decreased by modification, while T2 of capillary water increased. Furthermore, the moisture content and the amount of water in cell walls of modified wood were lower than for unmodified samples at the water-saturated state. Although the amount of accessible hydroxyl groups in modified wood did not show any significant difference compared with unmodified wood, the increase in T2 of capillary water indicates a decreased affinity of the wood cell wall to water. However, for the cell wall water, the physical confinement within the cell walls seemed to overrule the weaker wood–water interactions.

The potential of producing ecofriendly composites from industrial waste fibres, bonded with magnesium lignosulfonate, a lignin-based formaldehyde-free adhesive, was investigated in this work. Composites were produced in the laboratory using the following parameters: a hot press temperature of 210 &deg, C, a pressing time of 16 min, and a 15% gluing content of magnesium lignosulfonate (on the dry fibres). The physical and mechanical properties of the produced composites were evaluated and compared with the European Standard (EN) required properties (EN 312, EN 622-5) of common wood-based panels, such as particleboards for internal use in dry conditions (type P2), load-bearing particleboards for use in humid conditions (type P5), heavy-duty load-bearing particleboards for use in humid conditions (type P7), and medium-density fibreboards (MDF) for use in dry conditions. In general, the new produced composites exhibited satisfactory mechanical properties: a bending strength (MOR) (18.5 N&middot, mm&minus, 2) that was 42% higher than that required for type P2 particleboards (13 N&middot, 2) and 16% higher than that required for type P5 particleboards (16 N&middot, 2). Additionally, the modulus of elasticity (MOE) of composites (2225 N&middot, 2) was 24% higher than that required for type P2 particleboards (1800 N&middot, 2) and equivalent to the required MOE of MDF panels for use in dry conditions (2200 N&middot, 2). However, these ecofriendly composites showed deteriorated moisture properties, i.e., 24 h swelling and 24 h water absorption, which were a distinct disadvantage. This should be further investigated, as modifications in the lignosulfonate formula used and/or production parameters are necessary.