Lignins are the most important aromatic renewable natural resource today, serving as a sustainable, environmentally acceptable alternative feedstock to fossil‐derived chemicals and polymers in a vast scope of value‐added applications. Lignin is a biopolymeric molecule that, together with cellulose, is a fundamental component of higher vascular plants structural cell walls. It can be extracted from by‐products of the pulp and paper industries, agricultural waste and residues, and biorefinery products. Lignin properties may vary depending on source and extraction method with carbon and aromatic as the main compositions in lignin structure. These rich compositions make lignin more valuable, allowing for the creation of high‐value‐added green composites. However, the complex structure of lignin creates low reactivity to interact with crosslinker, and hence chemical modification is substantial to overcome this problem. This review aimed to present and discuss lignin structure, variation of lignin chemical properties regarding its source and extraction process, recent advances in chemical modification of lignin to enhance its reactivity, and potential applications of modified lignin for manufacturing value‐added biocomposites with enhanced properties and lower environmental impact, such as food handling/packaging, seed coating, automotive devices, 3D printing, rubber industry, and wood adhesives.

The efficient isolation process and understanding of lignin properties are essential to determine key features and insights for more effective lignin valorization as a renewable feedstock for the production of bio-based chemicals including wood adhesives. This study successfully used dilute acid precipitation to recover lignin from black liquor (BL) through a single-step and ethanol-fractionated-step, with a lignin recovery of ~35% and ~16%, respectively. The physical characteristics of lignin, i.e., its morphological structure, were evaluated by scanning electron microscopy (SEM). The chemical properties of the isolated lignin were characterized using comprehensive analytical techniques such as chemical composition, solubility test, morphological structure, Fourier-transform infrared spectroscopy (FTIR), 1H and 13C Nuclear Magnetic Resonance (NMR), elucidation structure by pyrolysis-gas chromatography-mass spectroscopy (Py-GCMS), and gel permeation chromatography (GPC). The fingerprint analysis by FTIR detected the unique peaks corresponding to lignin, such as C=C and C-O in aromatic rings, but no significant differences in the fingerprint result between both lignin. The 1H and 13C NMR showed unique signals related to functional groups in lignin molecules such as methoxy, aromatic protons, aldehyde, and carboxylic acid. The lower insoluble acid content of lignin derived from fractionated-step (69.94%) than single-step (77.45%) correlated to lignin yield, total phenolic content, solubility, thermal stability, and molecular distribution. It contradicted the syringyl/guaiacyl (S/G) units’ ratio where ethanol fractionation slightly increased syringyl unit content, increasing the S/G ratio. Hence, the fractionation step affected more rupture and pores on the lignin morphological surface than the ethanol-fractionated step. The interrelationships between these chemical and physicochemical as well as different isolation methods were investigated. The results obtained could enhance the wider industrial application of lignin in manufacturing wood-based composites with improved properties and lower environmental impact.

Extensive sample preparation procedures are required to analyze natural organic matter (NOM) in soil and sediment samples due to the mineral matrix. The preparation procedure not only requires a large amount of sample (typically more than 50 mg), but NOM extraction is frequently incomplete. In this study, 2–5 μg of solid NOM or 500 μg of unprocessed soil samples were fixed on a metal plate using double-sided adhesive tape and analyzed directly using laser desorption ionization (LDI) and ultrahigh resolution mass spectrometry (UHR-MS). Most of the peaks reported in previous LDI UHR-MS studies using NOM solutions were observed, and an additional ∼2200 unique peaks were found by analyzing the fulvic acids direct solid phase. Differences in the molecular composition of NOM in solid samples were seen clearly with minimum sample preparation. Lignin- and tannin-type molecules were detected in both Elliott soil and topsoil from Kyungpook National University campus. The data presented in this study demonstrate a proof-of-principle that highly sensitive, direct, molecular level analysis of solid-phase NOM from unprocessed soil samples and minimum sample preparation is possible.

Lignin is the second most naturally abundant biopolymer in the cell wall of lignocellulosic compound (15-35%) after cellulose.Lignin can be generated in massive amounts as by-products in biorefineries and pulp and paper industries through differing processes. Most lignin is utilized as generating energy and has always been treated as waste. Due to the high amount of phenolic compounds in lignin, it is considered as a potential material for various polymers, building blocks, and biomaterials production. Even though lignin can be utilized in the form of isolated lignin directly, the modification of lignin can increase the wide range of lignin applications. Lignin-based copolymers and modified lignin show better miscibility with another polymeric matrix, outstanding to the enhanced performance of such lignin-based polymer composites.This article summarizes the properly updated information of lignin’s potential applications, such as bio-surfactant, active packaging, antimicrobial agent, and supercapacitor.Keywords: active packaging, antimicrobial agent, bio-surfactant, lignin, supercapacitor