Optimizing the Dielectric and Mechanical Performance of 3D-Printed Cellulose-Based Biocomposites and Bionanocomposites through Factorial Design for Electrical Insulation Application.

Materials for low-permittivity and electrical insulation applications need to be re-engineered to achieve sustainable development. To address this challenge, the proposed study focused on the dielectric and mechanical optimization of 3D-printed cellulose-based composites for electrical insulation applications. Two different fillers, microcrystalline cellulose (MCC) and nanocrystalline cellulose (NCC), were used to create biocomposites and bionanocomposites, respectively, blended into a polylactic acid (PLA) matrix. The effects of infill ratio, printing temperature, and filler content on dielectric and mechanical properties were measured using an incomplete L9 (3^3) factorial design. The findings showed that the infill ratio was the most significant factor influencing the properties tested, directly attributable to the increase in material availability for polarization and mechanical performance. The second most influential factor was the filler content, increasing the polarity of the tested composites and decreasing the toughness of the biocomposites and bionanocomposites. Finally, printing temperature had no significant effect. Results for the biocomposites at a 50% infill ratio, 200 °C printing temperature, and a weight content of MCC of 15% gave a 60% higher tensile-mode stiffness than neat PLA printed under the same conditions, while exhibiting lower dielectric properties than neat PLA printed with a 100% infill ratio. These results pave the way for new lightweight materials for electrical insulation.

Activities of cellulose acetate and microcrystalline cellulose on the thermal and morphomechanical performances of a biobased hybrid composite made polybutylene succinate.

Microcrystalline cellulose (MCC-30 wt%) was extruded with a blend of polybutylene succinate (PBS) and cellulose acetate (CADS=2.5-20 wt%) to produce two grades of binary (PBS/CA, PBS/MCC) and ternary (PBS/CA/MCC) specimens by injection into a mold previously thermostated at 22 °C and 78 °C. The structure-property relationships of neat PBS (n-PBS) and PBS-based blends were investigated by Fourier transform infrared (FTIR) spectroscopy, diffuse reflectance infrared Fourier transform (DRIFT) spectroscopy, scanning electron microscopy (SEM), rheology, differential scanning calorimetry (DSC), thermogravimetry, and mechanical (tensile, bending) tests. FTIR/DRIFT outcomes revealed physical interactions between the ingredients through hydrogen bonds. Rheology and SEM evidenced the presence of entanglements and micro-voids absent in n-PBS. Non-isothermal DSC showed that 22 °C-molded formulations displayed crystalline degrees higher than 78 °C-specimens, except for PBS/MCC. DSC-isothermal analysis showed a hindrance effect of CA on PBS/CA crystallinity and a nucleating impact of MCC on PBS/MCC. Tensile and bending moduli increased for both material grades while the elongation at break decreased. Entanglements and micro-voids had detrimental effects on stress levels because the maximum tensile strength decreased when each or both biofillers were added to PBS. These structural configurations were beneficial for bending strengths since all blends' stiffness relatively increased regardless of material grade.

A Comparative Study on Heavy Metal Removal from CCA-Treated Wood Waste by Yarrowia lipolytica: Effects of Metal Stress.

Bioremediation is an effective way to remove heavy metals from pollutants. This study investigated the effects of Yarrowia lipolytica (Y. lipolytica) on the bioremediation of chromated copper arsenate (CCA)-treated wood wastes. Copper ions stressed the yeast strains to improve their bioremediation efficiency. A comparison of changes in morphology, chemical composition, and metal content of CCA wood before and after bioremediation was conducted. The amount of arsenic (As), chromium (Cr), and copper (Cu) was quantified by microwave plasma atomic emission spectrometer. The results showed that yeast strains remained on the surface of CCA-treated wood after bioremediation. The morphologies of the strains changed from net to spherical because of the Cu2+ stress. Fourier-transform infrared spectroscopy showed that carboxylic acid groups of wood were released after removing heavy metals. A large amount of oxalic acid was observed when the optical density (OD600nm) was 0.05 on the 21st day. Meanwhile, the highest removal rate of Cu, As, and Cr was 82.8%, 68.3%, and 43.1%, respectively. Furthermore, the Cu removal from CCA-treated wood increased by about 20% after Cu2+ stress. This study showed that it is feasible to remove heavy metals from CCA-treated wood by Y. lipolytica without destroying the wood structure, especially by copper-induced Y. lipolytica.

Fire Behavior and Failure Model of Multilayered Wood Flour/HDPE/Polycarbonate Composites with a Sandwich Structure.

The flame retardancy of wood-polymer composites significantly affects their potential applications. Thus, multilayered wood flour/high-density polyethylene (HDPE)/polycarbonate (PC) composites were prepared via thermocompression to improve the fire retardancy of wood-polymer composites in this paper. Thermal degradation behavior, flame retardancy, and flexural strengths of the resulting composites were investigated using a thermogravimetric analysis, cone calorimetry, and mechanical testing machine, respectively. Results revealed that the boric acid treatment reduced the heat release rate and total heat release of the wood flour/HDPE composites and increased their mass of residues. However, boric acid reduced the flexural strength of the resulting composites. The combustion test indicated that PC cap layers suppressed the combustion of the resulting composites via the formation of carbon layers. Adding PC layers reduced heat release and increased the flexural strength of the resulting composites. Finally, the failure mode of the multilayered wood flour/HDPE/PC composites in the three-point flexural test was simulated by finite element analysis.

Synthesis and Characterization of Wood Rigid Polyurethane Composites.

Incorporating biodegradable reinforcement, such as wood particles, into rigid polyurethane foams (RPUFs) is among the alternatives to reduce their environmental impact. This study aims to assess the effect of different wood particles as reinforcement in RPUFs. Reinforced rigid polyurethane foams are synthesized with milled wood particles of various forms and sizes and commercial polyol and isocyanate. The effect of fiber treatments and mechanical stirring on foams' properties is also studied. Additional tests on polyisocyanurate foams (PIR) were undertaken to assess the effect of reinforcement on their properties. Mechanical properties are measured to investigate the impact of wood particle reinforcement on the foam. Confocal microscopy and Fourier-transform infrared spectroscopy (FTIR) showed the interaction between the wood fibers and the matrix. Despite the adhesion observed for some fibers, most of the cell walls of RPUFs were punctured by the rigid wood fibers, which explained the decrease in the compressive strength of the composites for manually mixed foams. Mechanical stirring proved to be an efficient method to enhance the reinforcement power of untreated fibers. RPUF foams' properties showed similar changes when untreated wood flour was introduced to the formula, increasing compressive strength significantly.

A paradigm shift towards production of sustainable bioenergy and advanced products from Cannabis/hemp biomass in Canada.

The global cannabis (Cannabis sativa) market was 17.7 billion in 2019 and is expected to reach up to 40.6 billion by 2024. Canada is the 2nd nation to legalize cannabis with a massive sale of $246.9 million in the year 2021. Waste cannabis biomass is managed using disposal strategies (i.e., incineration, aerobic/anaerobic digestion, composting, and shredding) that are not good enough for long-term environmental sustainability. On the other hand, greenhouse gas emissions and the rising demand for petroleum-based fuels pose a severe threat to the environment and the circular economy. Cannabis biomass can be used as a feedstock to produce various biofuels and biochemicals. Various research groups have reported production of ethanol 9.2-20.2 g/L, hydrogen 13.5 mmol/L, lipids 53.3%, biogas 12%, and biochar 34.6% from cannabis biomass. This review summarizes its legal and market status (production and consumption), the recent advancements in the lignocellulosic biomass (LCB) pre-treatment (deep eutectic solvents (DES), and ionic liquids (ILs) known as "green solvents") followed by enzymatic hydrolysis using glycosyl hydrolases (GHs) for the efficient conversion efficiency of pre-treated biomass. Recent advances in the bioconversion of hemp into oleochemicals, their challenges, and future perspectives are outlined. A comprehensive insight is provided on the trends and developments of metabolic engineering strategies to improve product yield. The thermochemical processing of disposed-off hemp lignin into bio-oil, bio-char, synthesis gas, and phenol is also discussed. Despite some progress, barricades still need to be met to commercialize advanced biofuels and compete with traditional fuels.

Copper-Doped Carbon Nanodots with Superior Photocatalysis, Directly Obtained from Chromium-Copper-Arsenic-Treated Wood Waste.

An ecofriendly approach was developed for preparing copper-doped carbon dots (CDs) with superior photocatalysis using chromium-copper-arsenic (CCA)-treated wood waste as a precursor. Original wood (W-CDs), CCA-treated wood (C-CDs), and bioremediation CCA wood (Y-CDs) were used as the precursors. The chemical composition and structural, morphological, and optical properties, as well as the photocatalytic ability of the synthesized CDs varied with wood type. The C-CDs and W-CDs had similar characteristics: quasispherical in shape and with a diameter of 2 to 4.5 nm. However, the Y-CDs particles were irregular and stacked together, with a size of 1.5-3 nm. The presence of nitrogen prevented the formation of an aromatic structure for those CDs fabricated from bioremediation CCA wood. The three synthesized CDs showed a broad absorption peak at 260 nm and a weak absorption peak at 320 nm. Proof of the model study for the fabrication of luminescent CDs from CCA wood waste for bioimaging was provided. The degradation rate of CD photocatalytic MB was 97.8% for 30 min. Copper doping gives the CDs electron acceptor properties, improving their photocatalytic efficiency. This study provides novel ways to prepare nanomaterials from decommissioned wood as a nontoxic and low-cost alternative to fluorescent dots.

Fire Retardancy, Water Absorption, and Viscoelasticity of Borated Wood-Polycarbonate Biocomposites.

Demand for high-performance biocomposites is increasing due to their ease of processing, low environmental impact, and in-service performance. This study investigated the effect of boric acid modification of wood flour on polycarbonate (PC) wood composites' thermal stability, fire retardancy, water absorption, and creep behavior. The composites' fire retardancy increased with increasing wood flour content, and their char residue increased by 102.3% compared to that of pure PC. However, the water absorption of the resulting composites increased due to the hydroxyl groups of the wood flour. Wood flour also improved the composites' anti-creep properties. The excellent fire retardancy and anti-creep properties of wood-PC composites expand their use in the construction sector.

Microbial remediation for the removal of inorganic contaminants from treated wood: Recent trends and challenges.

Owing to the seriousness of the ecological risk and human hazard of inorganic wood preservatives, their effective removal was gradually recognized. This paper details different types of wood preservatives, their perniciousness, and their potential removal alternatives, while the wood treatment process is briefly described. Among decontamination methods, microbial remediation is considered as an environmentally friendly approach with enormous potentialities over the conventional treatments. In the current review, the mechanism of bioremediation is summed up and recent advances, challenges, and future perspectives of microbial remediation are discussed. The removal of heavy metals from treated wood requires a combination of various technologies to obtain higher performance. Meanwhile, the decontaminated wood generated through bioremediation can be effectively reused.

Conversion of lignocellulose into biochar and furfural through boron complexation and esterification reactions.

The aim of this work was to study the conversion of lignocellulose into biochar and furfural through boron complexation and esterification reaction. Boric acid was used to modify lignocellulose to obtain a high biochar yield boron-lignocellulosic material through complexation and esterification reactions. Furthermore, clean furfural was obtained as the gas products of boron-lignocellulosic materials pyrolysis. The structures of the boron-lignocellulosic materials were characterized, and their compound principle was revealed. Boric acid treatments increased the initial thermal degradation temperature of lignocellulose and promoted the formation of biochar and furfural. The biochar yield rate increased by 135.7% from 18.6 to 42.9% at 600 ℃ after 5% boric acid solution treatment. Compared with pure lignocellulose, cleaner and higher quantities of furfural were obtained from boron-lignocellulose pyrolysis. Finally, the possible chemical decomposition pathways of boron-lignocellulosic materials were identified. This study provides a new perspective on the thermochemical conversion of lignocellulose to furfural and biochar.

Effect of the Pyro-Gasification Temperature of Wood on the Physical and Mechanical Properties of Biochar-Polymer Biocomposites.

The physical and mechanical properties of wood (WPC) and biochar polymer composites (BPC) obtained at different pyro-gasification temperatures and different fiber proportions were investigated. Composite pellets made from wood chips or biochar and thermoplastic polymers (polypropylene or high-density polyethylene) were obtained by twin-screw extrusion, and test specimens were prepared by injection molding. Results showed that BPCs were more dimensionally stable compared to WPCs, but their mechanical properties decreased with increasing pyro-gasification temperatures due to the poor adhesion between the polymer and biochar. Indeed, FTIR investigations revealed the decrease or absence of hydroxyl groups on biochar, which prevents the coupling agent from reacting with the biochar surface. The change in the biochar chemical structure led to an improvement in the dimensional stability and hydrophobicity of the biocomposites. Despite the increased dimensional stability of BPCs compared to WPCs, BPCs still adsorb water. This was explained by the surface roughness and by the biochar agglomerations present in the composite. In conclusion, the thermochemical conversion of black spruce wood chips into biochar makes it brittle but more hydrophobic, thereby reducing the wettability of the BPCs.

Deinking sludge compost stability and maturity assessment using Fourier transform infrared spectroscopy and thermal analysis.

Thermal composting is an important and useful way to transfer raw organic matter into value-added product rich in humic substances. Furthermore, thermal composting is a very promising way to reduce deinking paper sludge pollutions, which are difficult to remove. The objective of this study was to investigate the behaviour of the composting process of deinking paper sludge with poultry manure over 14 months. Two composts were used: C1 (70/30: deinking paper sludge/poultry manure) and C2 (50/50: deinking paper sludge/poultry manure). The compost stability and maturity were assessed via physico-chemical and thermal analyses: thermogravimetric analysis, differential thermal analysis and diffuse reflectance infrared Fourier transform spectroscopy. Diffuse reflectance infrared Fourier transform spectroscopy analysis provided chemical information for the presence of aromatic, phenolic, aliphatic and polysaccharidic structures. Thermogravimetry analyses revealed that both deinking paper sludge composts were rich in humic acids. The ratio E4/E6 (fulvic acids/humic acids) was also carried out to characterise the maturity index of composts. After 14 months, the compost C2 is more stable, mature and rich in humic acids than compost C1. Furthermore, the addition of poultry manure to the deinking paper sludge-based composts enhanced the formation of humic substances. From 0 to 14 months of composting, the concentration of polychlorinated biphenyls decreased from 0.2 to 0.1 mg kg-1 and from 0.6 to 0.2 mg kg-1 for C1 and C2, respectively.

Production, characterization, and potential of activated biochar as adsorbent for phenolic compounds from leachates in a lumber industry site.

There is growing interest in low-cost, efficient materials for the removal of organic contaminants in municipal and industrial effluents. In this study, the efficiency of biochar and activated biochar, as promising adsorbents for phenol removal, was investigated at high (up to 1500 mg L-1) and low concentrations (0.54 mg L-1) in synthetic and real effluents (from wood-residue deposits in Québec), respectively. The performance of both materials was then evaluated in batch adsorption experiments, which were conducted using a low solid/liquid ratio (0.1 g:100 mL) at different phenol concentrations (C0 = 5-1500 mg L-1), and at 20 °C. Activated biochars presented higher phenol adsorption capacity compared to biochars due to their improved textural properties, higher micropore volume, and proportion of oxygenated carbonyl groups connected to their surface. The sorption equilibrium was reached within less than 4 h for all of materials, while the Langmuir model best described their sorption process. The maximum sorption capacity of activated biochars for phenol was found to be twofold relative to biochars (303 vs. 159 mg g-1). Results also showed that activated biochars were more effective than biochars in removing low phenol concentrations in real effluents. In addition, 95% of phenol removal was attained within 96 h (although 85% was removed after 4 h), thus reaching below the maximum authorized concentration allowed by Québec's discharge criteria (0.05 mg L-1). These results show that activated biochars made from wood residues are promising potential adsorbent materials for the efficient treatment of phenol in synthetic and real effluents.