Rynno Lohmus

This study presents the synthesis and characterisation of cellulose long chain fatty acid ester films using a novel distillable ionic liquid (IL), 5-methyl-1,5,7-triaza-bicyclo-[4.3.0] non-6-enium acetate [mTBNH][OAc] in combination with DMSO as a cosolvent. The cellulose esters cellulose diacetate (CDA), cellulose laurate (CL), and cellulose palmitate (CP) were fabricated through an evaporation-induced phase separation method (EIPS) and dried under two conditions: conventional oven drying (RO) and vacuum oven drying (VO). The influence of drying conditions on the structural, thermal, and surface properties of the films was evaluated using XRD, TGA, SEM, AFM, and contact angle measurement techniques. XRD confirmed an amorphous structure in all films, with no significant effect on the drying conditions. TGA revealed consistent thermal degradation profiles across all samples, with ester group decomposition accruing between 140 and 250 °C and main cellulose backbone degradation near 350 °C. The SEM cross-section showed a uniform film, devoid of cavities and layered structures. AFM analysis demonstrated that VO-dried films had smoother surfaces compared to RO-dried films, correlating with increased contact angles and enhanced hydrophobicity. A strong inverse relationship between surface roughness and hydrophobicity was observed, particularly in VO-dried samples, although this was not statistically significant due to data variability. Overall, the drying method had minimal impact on the internal structure and thermal stability; it significantly influenced surface morphology and wettability.

Since direct laser surface texturing of polymers is an emerging area, considerable attention is given to this technique with the aim of forming a basis for follow-up research that could open the way for potential technological ideas and optimization in novel applications. Laser pre-processing of ballistic textiles can raise surface roughness of smooth para-aramid fibres and as a result can improve the adhesion of functional coatings applied in following processing steps, thus opening new possibilities for material performance improvement. The impact resistance of ballistic fabric depends on the ability of its yarns in contact with the projectile absorb energy locally and disperse it to adjacent yarns without undergoing severe damage or failure. In addition to the yarn deformation and fracture, yarn resistance to pull-out contributes to the dissipation of impact energy significantly. The objective of this study is to optimize Kevlar^® KM2+ fabric surface topographies by adjusting the continuous wave (CW) CO₂ laser parameters in such a way that it increases the surface roughness and resistance to the yarn pull-out from the fabric without destroying the unique structure of the of Kevlar^® KM2+ fibres. Experimental research measured data show increase in surface roughness by 50–53% and set of laser parameter variants have been obtained that allow for an increase in KM2+ 440D woven fabric yarns pull out force from fabric in the range from 50% up to 99% compared to the untreated one.

Fiber-reinforced plywood is a composite material that combines the natural strength and rigidity of plywood with the added durability and resilience provided by reinforcing fibers. This type of plywood is designed to offer improved characteristics over standard plywood, including enhanced strength, stiffness, resistance to impact and moisture, and environmental degradation. By integrating reinforcing fibers, such as glass, carbon, or natural fibers (like flax, bamboo, or hemp) into or onto plywood, manufacturers can create a material that is better suited for applications where traditional plywood might fall short or when a decrease in product weight or savings in wood raw material are necessary. This report reviews the current progress in fiber-reinforced plywood in the context of plywood as a construction material to better understand the potential gains in plywood applications, mechanical parameters, and material savings. It is found that a simple and cost-effective procedure of fiber reinforcement allows for substantial improvements in plywood’s mechanical properties, typically to the extent of 10–40%. It is suggested that the wider adoption of fiber-reinforced plywood, especially in load- and impact-bearing applications, would greatly contribute to enhanced durability and longevity of the material while also allowing for more sustainable use of raw wood material.

Cell-penetrating peptides (CPPs) are highly promising transfection agents that can deliver various compounds into living cells, including nucleic acids (NAs). Positively charged CPPs can form non-covalent complexes with negatively charged NAs, enabling simple and time-efficient nanoparticle preparation. However, as CPPs have substantially different chemical and physical properties, their complexation with the cargo and characteristics of the resulting nanoparticles largely depends on the properties of the surrounding environment, i.e., solution. Here, we show that the solvent used for the initial dissolving of a CPP determines the properties of the resulting CPP particles formed in an aqueous solution, including the activity and toxicity of the CPP–NA complexes. Using different biophysical methods such as dynamic light scattering (DLS), atomic force microscopy (AFM), transmission and scanning electron microscopy (TEM and SEM), we show that PepFect14 (PF14), a cationic amphipathic CPP, forms spherical particles of uniform size when dissolved in organic solvents, such as ethanol and DMSO. Water-dissolved PF14, however, tends to form micelles and non-uniform aggregates. When dissolved in organic solvents, PF14 retains its α-helical conformation and biological activity in cell culture conditions without any increase in cytotoxicity. Altogether, our results indicate that by using a solvent that matches the chemical nature of the CPP, the properties of the peptide–cargo particles can be tuned in the desired way. This can be of critical importance for in vivo applications, where CPP particles that are too large, non-uniform, or prone to aggregation may induce severe consequences.

Polydimethylsiloxane (PDMS) is the most widely used silicon-based polymer due to its versatility and its various attractive properties. The fabrication of PDMS involves liquid phase cross-linking to obtain hydrophobic and mechanically flexible material in the final solid form. This allows to add various fillers to affect the properties of the resulting material. PDMS has a relatively low Thermal Conductivity (TC), in the order of 0.2 W/mK, which makes it attractive for thermal insulation applications such as sealing in construction. Although a further decrease in the TC of PDMS can be highly beneficial for such applications, most research on the thermal properties of PDMS composites have focused on fillers that increase the TC rather than decrease it. In the present work, we propose a simple and reliable method for making a PDMS-based composite material with significantly improved thermal insulation properties, by adding hollow glass microspheres (HGMs) to the mixture of the liquid base and the cross-linker (10:1 ratio), followed by degassing and heat-assisted crosslinking. We obtained a 31% reduction of thermal conductivity and a 60% increase in the elastic modulus of samples with HGM content of 17% by weight. At the same time, the sound insulation capacity of the PDMS-HGM composite is slightly decreased in comparison to pure PDMS, as a result of its lower density. Finally, the wettability of the samples had no dependence on HGM content.

The reinforcement of plywood is demonstrated by laminating pretensioned basalt fibers between veneer sheets, to fabricate so-called prestressed plywood. Belt type basalt fibers bearing a specific adhesion promoting silane sizing were aligned between veneer sheets with 20 mm spacing and were pretensioned at 150 N. Three-layer plywood samples were prepared and tested for tensile strength at room temperature and at 150 °C. The room temperature tensile tests revealed a 35% increase in tensile strength for prestressed plywood compared to that of the conventional specimen. The reinforcement effect deteriorated at 150 °C but was restored upon cooling to room temperature. The deterioration is attributed to the weakening of bonding between the basalt fibers and phenolic resin matrix at elevated temperatures due to the softening of the resin.

Adhesion forces between functionalized gold colloidal nanoparticles (Au NPs) and scanning probe microscope silicon tips were experimentally investigated by atomic force microscopy (AFM) equipped with PeakForce QNM (Quantitative Nanoscale Mechanics) module. Au NPs were synthesized by a seed-mediated process and then functionalized with thiols containing different functional groups: amino, hydroxy, methoxy, carboxy, methyl, and thiol. Adhesion measurements showed strong differences between NPs and silicon tip depending on the nature of the tail functional group. The dependence of the adhesion on ligand density for different thiols with identical functional tail-group was also demonstrated. The calculated contribution of the van der Waals (vdW) forces between particles was in good agreement with experimentally measured adhesive values. In addition, the adhesion forces were evaluated between flat Au films functionalized with the same molecular components and silicon tips to exclude the effect of particle shape on the adhesion values. Although adhesion values on flat substrates were higher than on their nanoparticle counterparts, the dependance on functional groups remained the same.