A complete bibliometric analysis of the Scopus database was performed to identify the research trends related to lignin valorization from 2000 to 2016. The results from this analysis revealed an exponentially increasing number of publications and a high relevance of interdisciplinary collaboration. The simultaneous valorization of the three main components of lignocellulosic biomass (cellulose, hemicellulose, and lignin) has been revealed as a key aspect and optimal pretreatment is required for the subsequent lignin valorization. Research covers the determination of the lignin structure, isolation, and characterization; depolymerization by thermal and thermochemical methods; chemical, biochemical and biological conversion of depolymerized lignin; and lignin applications. Most methods for lignin depolymerization are focused on the selective cleavage of the β-O-4 linkage. Although many depolymerization methods have been developed, depolymerization with sodium hydroxide is the dominant process at industrial scale. Oxidative conversion of lignin is the most used method for the chemical lignin upgrading. Lignin uses can be classified according to its structure into lignin-derived aromatic compounds, lignin-derived carbon materials and lignin-derived polymeric materials. There are many advances in all approaches, but lignin-derived polymeric materials appear as a promising option.

A novel lignin-based slow release fertilizer with low environmental impact has been developed. More precisely, a granulated simple superphosphate fertilizer, consisting of calcium phosphate monobasic [Ca(H₂PO₄)₂·H₂O] and gypsum (CaSO₄·2H₂O) was coated with modified kraft lignins and the diffusion of phosphorus was observed as a function of time. The lignin was hydroxymethylated with formaldehyde and subsequently cross-linked with phenol-formaldehyde resin resulting in HML-PF as coating. Moreover, coating films were prepared from a mixture of acetylated lignin (L_ac) and acetylated cellulose (Cell_ac). Both coatings show similar permeability to calcium phosphate and controlled effectively the P-release, particularly at the initial stages of the experiment. The P-release was linear in the decay phase but there is no lag time in the process. A significant P amount was not released from the particles coated with HML-PF, i.e. 80–50% remained irreversible bound, depending on the coating formulation. The maximum fractional P-release varied among the different coatings tested. Phosphorus is partly retained inside the slightly soluble calcium sulfate matrix.

In the last decade, the utilization of waste by-product apple pomace has been extensively researched (due to its difficult disposal) and currently finds beneficial usage in various industries; as substrate for microbial growth or recovery of pectin, xyloglucan and polyphenols. In this research apple juice was produced at pilot scale. Furthermore, apple pomace was employed as substrate for the production of pectin, biofuel (pellets) and concentrated apple pomace extract. Extensive mass and heat balances were conducted to evaluate the feasibility of this approach on industrial scale. The produced pellets had very similar characteristics to wood pellets (net calorific value of 20.3 MJ/kg). Dried apple pomace contained 11.9% of pectin. Fed-batch cultivation of baker´s yeast with apple pomace extract demonstrated a potential for partial substitution of molasses in industrial bioprocesses. This concept shows how a zero discharge biorefinery process converts waste from apple juice production into three valuable products enabling connections between different industries. Graphic Abstract