Monika A. Jedrzejczyk’s research while affiliated with Maastricht University and other places

A combined experimental and theoretical framework was developed that predicts the solvent fractionation of lignin, taking chemical and physical dispersity into account. This paves the way for a broader applicability of lignin in bio-based materials.

In this study, the development of lignin-based resins for wood adhesion applications was demonstrated. We investigated two lignin fractions: commercial Protobind 1000 lignin and methanol-soluble Protobind 1000 lignin fraction after mild solvolysis. Although lignin has previously been incorporated into various cross-linked systems, this is the first report on lignin-based thermosets obtained via thiol–yne “click” chemistry. In this approach, lignin was functionalized with terminal alkyne groups followed by cross-linking with a multifunctional thiol, resulting in polymeric network formation. The influence of the curing conditions on the resin characteristics and performance was studied, by varying the amount of reactive monomeric diluents. Additionally, a post-curing strategy utilizing the Claisen rearrangement was investigated. These resins were tested as a wood adhesive and were proven to possess a desirable performance, comparable to the state-of-art phenol-formaldehyde resins. Lignin-based thiol–yne resins turn out to be an alternative to phenol-formaldehyde resins, currently used as adhesives and coatings. Although it is possible to use lignin in phenol-formaldehyde resins, lignin addition is compromising the resin’s performance. The main benefits over the phenol-formaldehyde approach are that higher lignin loadings are possible to achieve, and no volatiles are emitted during the resin processing and use.

The synthesis of novel, renewable lignin‐based protective films with anticorrosive properties is presented in this work. Thermosetting films are prepared by means of tandem UV‐initiated thiol‐yne “click” synthesis and Claisen rearrangement strategy. These films contain high lignin loading, 46–61%, originating from a birch wood reductive catalytic fractionation process using a nickel catalyst. Lignin fractions with varying monomer content are compared before resins preparation, namely a mixture of monomers and oligomers without fractionation, or after fractionation via extraction and membrane separation. This study aims to determine if separation of lignin monomers and oligomers is necessary for the application as a thermosetting polymeric resin. The resulting protective films exhibit remarkable adhesion to a metal surface and excellent solvent resistance, even after exposure to corrosive environment. Moreover, those films show superior barrier properties, studied with Odd Random Phase Electrochemical Impedance Spectroscopy. After 21 days of exposure, the examined films still show impressive high corrosion protection with the low frequency impedance around 1010 Ωcm2 and capacitive behavior. This work demonstrates an interesting proof‐of‐concept where laborious, costly and energy‐intensive separation of the depolymerized lignin mixture of monomers and oligomers is not necessary for the successful resin synthesis with excellent properties using the applied synthetic strategy. This article is protected by copyright. All rights reserved

There is an environmental concern regarding the use of petroleum-based lubricants, which are generally toxic and nonbiodegradable. Biobased lubricants, such as vegetable oils, are the alternative: they show excellent lubricity, are readily biodegradable and nontoxic. However, a major disadvantage of using vegetable oils in lubricant applications is their lack of thermo-oxidative stability, which can be improved by antioxidant additives. Here, we propose the use of lignin-based additives in biolubricant formulations to improve this feature, based on lignin’s known antioxidant properties. To ensure a stable dispersion in vegetable oil, lignin was partially esterified. Antioxidant properties of lignin before and after palmitoylation were demonstrated in a 2,2-diphenyl-1-picrylhydrazyl (DPPH) assay. Four different lignin-based fractions, commercial Protobind P1000 soda lignin from straw, solvolytically fractionated Protobind P1000 lignin and two lignin fractions from reductively catalyzed fractionation (RCF) of native birch wood, were tested in biolubricant formulations with castor oil as base oil. Those lignin fractions exhibited excellent performance compared to butylated hydroxytoluene (BHT), a commonly used petroleum-based antioxidant. Formulations of modified lignin in castor oil possess improved thermo-oxidative stability, as illustrated by their increased oxidation induction time. Additionally, rheological and tribological tests demonstrate similar, or in some cases improved, lubricating properties compared to castor oil. This study showcases the successful incorporation of lignin-based antioxidants in biolubricant formulations, tackling the major disadvantage of vegetable oils as environment-friendly lubricants.

There is an increasing urge to make the transition toward biobased materials. Lignin, originating from lignocellulosic biomass, can be potentially valorized as humic acid (HA) adsorbents via lignin-based mesoporous carbon (MC). In this work, these materials were synthesized for the first time starting from modified lignin as the carbon precursor, using the soft-template methodology. The use of a novel synthetic approach, Claisen rearrangement of propargylated lignin, and a variety of surfactant templates (Pluronic, Kraton, and Solsperse) have been demonstrated to tune the properties of the resulting MCs. The obtained materials showed tunable properties (BET surface area: 95–367 m²/g, pore size: 3.3–36.6 nm, VBJH pore volume: 0.05–0.33 m³/g, and carbon and oxygen content: 55.5–91.1 and 3.0–12.2%, respectively) and good performance in terms of one of the highest HA adsorption capacities reported for carbon adsorbents (up to 175 mg/g).