Lignin was isolated from wood wastes comprising Iroko sawdust (IR) and mixed sawdust from Iroko and Norway spruce (IRNS), furnished by a local wood houses producer. The respective acidolysis lignin fractions were structurally characterized using pyrolysis (Py)-GCMS, two-dimensional heteronuclear single quantum correlation nuclear magnetic resonance (2D HSQC NMR), Fourier-transform infrared FTIR and ultraviolet-visible (UV-VIS) spectroscopies, size exclusion chromatography, and standard wet-chemistry methods for Klason lignin and polysaccharides determination. The isolated lignin fractions were subsequently used for the preparation of lignin nanoparticles (LNPs) using a non-solvent method. LNPs were then used for wood surface treatment using a dip-coating technique. The coated wood samples were analyzed by colorimetry and scanning electron microscopy (SEM) before and after artificial weathering experiments in a UV chamber to investigate the UV protection potential of the LNPs coatings. Wood samples dip-coated with LNPs showed promising surface modifications resembling a sort of film of fused LNPs. Coatings made from IR-LNPs and IRNS-LNPs performed significantly better in artificial weathering experiments than uncoated reference samples.

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Lignin isolated from beech sawdust was used for the preparation of lignin nanoparticles (LNPs) with entrapped essential oil (EO) from cinnamon bark (Cinnamomum zeylanicum Blume), common thyme (Thymus vulgaris L.), and wild thyme (Thymus serpyllum L.) using a fast antisolvent method. Analysis of EO-loaded LNPs by pyrolysis-gas chromatography–mass spectrometry and Fourier transform infrared spectroscopy confirmed molecular interaction between EOs and LNPs. Quantification of EO incorporation into the LNPs and their in vitro release profiles were assessed by reversed phase high-performance liquid chromatography. Utilized EOs were, to different extents, successfully entrapped inside LNPs, which were attributed to extensive π-stacking between aromatic compounds in EOs like cinnamaldehyde, thymol, and carvacrol on one side and aromatic lignin units on the other side. In vitro release of common thyme and wild thyme EOs from EO-loaded LNPs was strongly delayed compared to the use of pure oil, giving a promising outlook for the development of new bio-based biocide delivery systems for wood preservation.

Hardwood timber is becoming increasingly important in Europe for its use as structural material, both as solid wood and engineered structural products. In Italy, the great abundance of beech forests has recently led to a research project to investigate the use of this species in construction. A first step is the characterization of the raw material for the production of structural glued products. This requires developing the strength grading of beech boards, both by visual and machine methods. To the aim, four provenances were collected across the distribution of beech in Italy. The main strength reducing characteristics were measured visually, and the dynamic modulus of elasticity was determined before performing the destructive bending tests of sampled boards. Correlation between properties were similar to what is usually observed for softwoods with the exception of density, which did not correlate with any other property. Several visual rules and machine settings were developed and compared, showing the effectiveness of both methods for the strength grading of beech. The grading yields for the high strength classes were very similar for machine and visual grading, while the machine permitted to reduce the number of rejected elements when two grades were selected at the same time.

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Lignin was isolated through mild acidolysis from local wood sources such as beech wood and chestnut wood sawdust, a high-volume side product of wood industries. The lignin fractions were characterized by pyrolysis-gas chromatography/mass spectrometry (Py-GC/MS), Fourier-transform infrared (FTIR), ultraviolet-visible (UV-Vis) and two-dimensional heteronuclear single-quantum correlation nuclear magnetic resonance (2D HSQC NMR) spectroscopies and size exclusion chromatography (SEC). The Klason lignin (KL) content and polysaccharide composition were determined using traditional methods. Lignin nanoparticles (LNPs) were preparedviaa non-solvent method involving dialysis and characterized by scanning electron microscopy (SEM) and transmission electron microscopy (TEM) and FTIR and UV-VIS spectroscopies. Semi-porous as well as hollow nanoparticles endowed with a spherical shape were observed. The large majority of the LNPs exhibited an average particle diameter of 90–120 nm. Dynamic light scattering (DLS) analysis showed that both distribution and frequency of dimensional classes of LNPs are clearly affected by the lignin solvent system, i.e. solvent selection governs the size distribution of LNPs.