Recently, lignin utilization in advanced applications has gained much interest. Due to the limitation of the current use of standard lignin, lignin particles have recently gained attention in overcoming the challenge. In this work, the spherical lignin particles obtained from organosolv lignin (OL) were prepared using the dialysis method with tetrahydrofuran (THF) or ethanol as the solvent. From the result, it was found that the types of lignin and solvent, initial lignin concentration, and stirring rate strongly affected the size of fabricated particles. Moreover, the preparation of lignin particles using THF as a solvent showed more uniform and symmetric spherical lignin particles. The stability of the particle dispersion was examined under various pH conditions. Moreover, lignin samples were also introduced into the poly(vinyl alcohol) (PVA) for the production of ultraviolet (UV)-blocking composite film. Mechanical and optical properties of composite film were also observed. As a result, the prepared lignin–PVA composite film showed great ultraviolet (UV) protective potential in both UVA and UVB regions.

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We develop a sequential fractionation of palm empty fruit bunches (EFB) and microwave-assisted depolymerization of lignin for producing monophenolic compounds with high yields. EFB has been known as a low-priced and abandoned residue from the palm oil milling process due to its low heating value and generation of toxic gases upon burning; therefore, valorization of EFB has been an important task for circular economy. In this study, a subsequent alkaline hot compressed water fractionation to separate hemicellulose and lignin from cellulose has been studied. The lignin separation by lignin precipitation and a filtration process followed by microwave-assisted lignin oxidative depolymerization to high value phenolic compounds was proposed. We systematically screened many catalysts as well as investigated reaction conditions (such as the concentration of hydrogen peroxide, reaction time, etc.) to achieve the highest yield of lignin-derived phenolic compounds. It was found that the optimal conditions for depolymerization of pretreated EFB lignin were (i) NaOH solution with 2.5% (w/w) hydrogen peroxide, (ii) microwave (300 W) for 15 min, and (iii) bimetallic Cu­(OH)2 and Fe2O3 catalysts. The highest percentage of the total phenolic compound concentration peak area is 91.78%, including 42.84% of syringol, 5.42% of vanillin, 8.71% of acetovanillone, 6.65% of syringaldehyde, and 28.16% of acetosyringone. The proposed sequential fractionation and microwave-assisted treatment would be promising for converting other lignocellulosic raw biomass to useful phenolic compounds.

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This work aims to enhance the value of palm empty fruit bunches (EFBs), an abundant residue from the palm oil industry, as a precursor for the synthesis of luminescent carbon dots (CDs). The mechanism of fIuorimetric sensing using carbon dots for either enhancing or quenching photoluminescence properties when binding with analytes is useful for the detection of ultra-low amounts of analytes. This study revealed that EFB-derived CDs via hydrothermal synthesis exceptionally exhibited luminescence properties. In addition, surface modification for specific binding to a target molecule substantially augmented their PL characteristics. Among the different nitrogen and sulfur (N and S) doping agents used, including urea (U), sulfate (S), p-phenylenediamine (P), and sodium thiosulfate (TS), the results showed that PTS-CDs from the co-doping of p-phenylenediamine and sodium thiosulfate exhibited the highest PL properties. From this study on the fluorimetric sensing of several metal ions, PTS-CDs could effectively detect Fe3+ with the highest selectivity by fluorescence quenching to 79.1% at a limit of detection (LOD) of 0.1 µmol L−1. The PL quenching of PTS-CDs was linearly correlated with the wide range of Fe3+ concentration, ranging from 5 to 400 µmol L−1 (R2 = 0.9933).

Hydrodeoxygenation (HDO) of bio-oil derived from liquefaction of a palm empty fruit bunch (EFB) in glycerol was investigated. To enhance the heating value and reduce the oxygen content of upgraded bio-oil, hydrodeoxygenation of light bio-oil over Ni- and Co-based catalysts on an Al2O3 support was performed in a rotating-bed reactor. Two consecutive steps were conducted to produce bio-oil from EFB including (1) microwave-assisted wet torrefaction of EFB and (2) solvothermolysis liquefaction of treated EFB in a Na2CO3/glycerol system. The HDO of as-prepared bio-oil was subsequently performed in a unique design reactor possessing a rotating catalyst bed for efficient interaction of a catalyst with bio-oil and facile separation of the catalyst from upgraded bio-oil after the reaction. The reaction was carried out in the presence of each mono- or bimetallic catalyst, namely, Co/Al2O3, Ni/Al2O3, NiMo/Al2O3, and CoMo/Al2O3, packed in the rotating-mesh host with a rotation speed of 250 rpm and kept at 300 and 350 °C, 2 MPa hydrogen for 1 h. From the results, the qualities of upgraded bio-oil were substantially improved for all catalysts tested in terms of oxygen reduction and increased high heating value (HHV). Particularly, the NiMo/Al2O3 catalyst exhibited the most promising catalyst, providing favorable bio-oil yield and HHV. Remarkably greater energy ratios and carbon recovery together with high H/O, C/O, and H/C ratios were additionally achieved from the NiMo/Al2O3 catalyst compared with other catalysts. Cyclopentanone and cyclopentene were the main olefins found in hydrodeoxygenated bio-oil derived from liquefied EFB. It was observed that cyclopentene was first generated and subsequently converted to cyclopentanone under the hydrogenation reaction. These compounds can be further used as a building block in the synthesis of jet-fuel range cycloalkanes.

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