Strategies for the Removal of Polysaccharides from Biorefinery Lignins: Process Optimization and Techno Economic Evaluation.

The utilization of biorefinery lignins as a renewable resource for the production of bio-based chemicals and materials remain a challenge because of the high polysaccharide content of this variety of lignins. This study provides two simple methods; (i) the alkaline hydrolysis-acid precipitation method and (ii) the acid hydrolysis method for the removal of polysaccharides from polymeric biorefinery lignin samples. Both purification strategies are optimized for two different hardwood hydrolysis lignins, HL1 and HL2, containing 15.1% and 10.1% of polysaccharides, respectively. The treated lignins are characterized by polysaccharide content, molecular weight, hydroxyl content, and Attenuated Total Reflection-Fourier Transform Infrared Spectroscopy (ATR-FTIR). Preliminary techno-economic calculations are also carried out for both purification processes to assess the economic potential of these technologies. The results indicate that both protocols could be used for the purification of HL1 and HL2 hydrolysis lignins because of the minimal polysaccharide content obtained in the treated lignins. Nevertheless, from an industrial and economic perspective the acid hydrolysis technology using low acid concentrations and high temperatures is favored over the alkaline hydrolysis-acid precipitation strategy.

Low molecular weight and highly functional RCF lignin products as a full bisphenol a replacer in bio-based epoxy resins.

Herein, we present a full lignocellulose-to-chemicals valorization chain, wherein low molecular weight and highly functional lignin oligomers, obtained from reductive catalytic fractionation (RCF) of pine wood, were used to fully replace bisphenol A (BPA) for synthesizing bio-based epoxy resins.

A sustainable wood biorefinery for low-carbon footprint chemicals production.

The profitability and sustainability of future biorefineries are dependent on efficient feedstock use. Therefore, it is essential to valorize lignin when using wood. We have developed an integrated biorefinery that converts 78 weight % (wt %) of birch into xylochemicals. Reductive catalytic fractionation of the wood produces a carbohydrate pulp amenable to bioethanol production and a lignin oil. After extraction of the lignin oil, the crude, unseparated mixture of phenolic monomers is catalytically funneled into 20 wt % of phenol and 9 wt % of propylene (on the basis of lignin weight) by gas-phase hydroprocessing and dealkylation; the residual phenolic oligomers (30 wt %) are used in printing ink as replacements for controversial para-nonylphenol. A techno-economic analysis predicts an economically competitive production process, and a life-cycle assessment estimates a lower carbon dioxide footprint relative to that of fossil-based production.

Reductive catalytic fractionation: state of the art of the lignin-first biorefinery.

Reductive catalytic fractionation (RCF) of lignocellulose is an emerging biorefinery scheme that combines biomass fractionation with lignin depolymerisation. Central to this scheme is the integration of heterogeneous catalysis, which overcomes the tendency of lignin to repolymerise. Ultimately, this leads to a low-Mw lignin oil comprising a handful of lignin-derived monophenolics in close-to-theoretical yield, as well as a carbohydrate pulp. Both product streams are considered to be valuable resources for the bio-based chemical industry. This Opinion article sheds light on recently achieved milestones and consequent research opportunities. More specifically, mechanistic studies have established a general understanding of the elementary RCF steps, which include (i) lignin extraction, (ii) solvolytic and catalytic depolymerisation and (iii) stabilisation. This insight forms the foundation for recently developed flow-through RCF. Compared to traditional batch, flow-through RCF has the advantage of (i) separating the solvolytic steps from the catalytic steps and (ii) being a semi-continuous process; both of which are beneficial for research purposes and for industrial operation. Although RCF has originally been developed for 'virgin' biomass, researchers have just begun to explore alternative feedstocks. Low-value biomass sources such as agricultural residues, waste wood and bark, are cheap and abundant but are also often more complex. On the other side of the feedstock spectrum are high-value bio-engineered crops, specifically tailored for biorefinery purposes. Advantageous for RCF are feedstocks designed to (i) increase the total monomer yield, (ii) extract lignin more easily, and/or (iii) yield unconventional, high-value products (e.g. alkylated catechols derived from C-lignin). Taking a look at the bigger picture, this Opinion article highlights the multidisciplinary nature of RCF. Collaborative efforts involving chemists, reactor engineers, bioengineers and biologists working closer together are, therefore, strongly encouraged.

Perspective on Lignin Oxidation: Advances, Challenges, and Future Directions.

Lignin valorization has gained increasing attention over the past decade. Being the world's largest source of renewable aromatics, its valorization could pave the way towards more profitable and more sustainable lignocellulose biorefineries. Many lignin valorization strategies focus on the disassembly of lignin into aromatic monomers, which can serve as platform molecules for the chemical industry. Within this framework, the oxidative conversion of lignin is of great interest because it enables the formation of highly functionalized, valuable compounds. This work provides a brief overview and critical discussion of lignin oxidation research. In the first part, oxidative conversion of lignin models and isolated lignin streams is reviewed. The second part highlights a number of challenges with respect to the substrate, catalyst, and operating conditions, and proposes some future directions regarding the oxidative conversion of lignin.

Alkane production from biomass: chemo-, bio- and integrated catalytic approaches.

Linear, branched and cyclic alkanes are important intermediates and end products of the chemical industry and are nowadays mainly obtained from fossil resources. In search for alternatives, biomass feedstocks are often presented as a renewable carbon source for the production of fuels, chemicals and materials. However, providing a complete market for all these applications seems unrealistic due to both financial and logistic issues. Despite the very large scale of current alkane-based fuel applications, biomass definitely has the potential to offer a partial solution to the fuel business. For the smaller market of chemicals and materials, a transition to biomass as main carbon source is more realistic and even probably unavoidable in the long term. The appropriate use and further development of integrated chemo- and biotechnological (catalytic) process strategies will be crucial to successfully accomplish this petro-to-bio feedstock transition. Furthermore, a selection of the most promising technologies from the available chemo- and biocatalytic tool box is presented. New opportunities will certainly arise when multidisciplinary approaches are further explored in the future. In an attempt to select the most appropriate biomass sources for each specific alkane-based application, a diagram inspired by van Krevelen is applied, taking into account both the C-number and the relative functionality of the product molecules.