Biorefineries, which process biomass feedstocks into valuable (bio)products, aim to replace fossil fuel-based refineries to produce energy and chemicals, reducing environmental and health hazards, including climate change, and supporting a sustainable economy. In particular, lignocellulose-based biorefineries, utilizing the most abundant renewable feedstock on Earth, have significant potential to supply sustainable energy, chemicals and materials. Ionic liquids (ILs, organic salts with low melting temperatures) and deep eutectic solvents (DESs, mixtures with eutectic points lower than the ideal mixture) are capable of dissolving some of the key lignocellulose polymers, and even the whole biomass. Furthermore, they have intrinsic advantages over molecular solvents, including safer usage profiles and high tunability, which allow tailored physicochemical properties. Such properties provide unique opportunities for the development of new processes that could unlock the full potential of future biorefineries. Here, we review the current state of lignocellulosic biomass processing with ILs and DESs, with a specific focus on the pretreatment chemistry, process flow and products from each component; followed by discussions on sustainability assessments and technological challenges. We aim to inform the research community about the opportunities, challenges and perspectives in developing truly sustainable lignocellulose-based biorefineries.

A systematic summary on the current state-of-art of the formation, identification, and further valorization of oligomeric products during various lignin depolymerization processes.

Nutrient pollution poses a significant global environmental threat, and addressing this issue remains an ongoing challenge. Biochar has been identified as a potential adsorbent for environmental remediation. However, raw biochar has a low nitrate adsorption capacity; thus, biochar modification is necessary for targeted environmental applications. This work explored and compared the performance of Fe-doped, N-doped, and N-Fe-co-doped biochars from Douglas fir toward nitrate removal from an aqueous solution. A central composite experimental design was used to optimize processing variables, maximizing the surface area and nitrate adsorption capacity. Proximate analysis, elemental composition, gas physisorption, XPS, SEM, TEM, FTIR, and XRD were used to characterize the biochar’s properties. Pyrolysis under NH₃ gas generated more pores in biochar than conventional pyrolysis. Doping biochar with N and Fe improved nitrate adsorption capacity from aqueous solutions. The maximum nitrate adsorption capacity of Fe-N-doped biochar produced at 800 °C was 20.67 mg g⁻¹ in sorption tests at pH 3.0. The formation of N-containing functional groups and Fe oxides on the biochar surface enhanced the nitrate removal efficiency of N-Fe biochar. The results indicate that biochar’s adsorption capacity for NO₃⁻ is largely affected by the solution’s pH and biochar’s surface chemistry. Electrostatic attraction is the primary mechanism for nitrate adsorption.

Schematic depiction of the approach used to screen different pretreatment solvents on different biomass feedstocks.

The rising global energy demand, alongside concerns regarding environmental deterioration due to the use of fossil fuels, has spurred extensive investigation into renewable energy alternatives. Biomass-derived biodiesel, especially from lesser-known oil sources, emerges as a promising option. This research focuses on analyzing the fatty acid methyl esters (FAMEs) derived from Kariya (Hildegardia barteri (Mast.) Kosterm) seed oil through basic catalytic transesterification using gas chromatography–flame ionization detector (GC–FID) analysis, assessing its potential as a biodiesel feedstock. Oil extraction from Kariya seeds was carried out using three solvents (n-hexane, ethanol, and a 1:1 blend of hexane and ethanol), followed by transesterification with methanol. Gas chromatography–mass spectrometry (GC–MS) and GC–FID analyses were utilized to identify and quantify FAMEs in the resulting biodiesel. The results revealed various FAMEs, including methyl myristate, methyl palmitate, methyl stearate, methyl oleate, methyl linoleate, and methyl linolenate. Significant differences in FAME composition were observed among the samples, with hexane–ethanol Kariya oil biodiesel (HE-KOB) showing the highest FAME content (76.1%). This combination of solvents exhibited synergistic effects on the composition of HE-KOB, suggesting potential optimization strategies for biodiesel production. Fourier transform infrared spectroscopy (FTIR) provided additional insights into the molecular composition of the biodiesel samples, confirming their biodiesel nature through the identified functional groups such as methyl, methylene, hydrocarbon, ester, aldehyde, and alkene. Thermogravimetric analysis (TGA) for thermal decomposition also gave an insight into FAME composition and its contribution to the degree of conversion of biodiesel to energy. These findings highlight the feasibility of utilizing Kariya seed oil as a biodiesel feedstock, emphasizing the importance of solvent selection and transesterification conditions in optimizing FAME yield and composition. This research contributes to the exploration of underutilized oil sources for sustainable biodiesel production, aligning with the global shift towards cleaner and renewable energy sources.