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Biomass pyrolysis has recently gained increasing attention as a thermochemical conversion process for obtaining value-added products, thanks to the development of cutting-edge, innovative and cost-effective pyrolysis processes. Over time, new and novel pyrolysis techniques have emerged, and these processes can be tuned to maximize the production of high-quality hydrogen. This review examines recent advancements in biomass pyrolysis by classifying them into conventional, advanced and emerging approaches. A comprehensive overview on the recent advancements in biomass pyrolysis, highlighting the current status for industrial applications is presented. Further, the impact of each technique under different approaches on conversion of biomass for hydrogen production is evaluated. Techniques, such as inline catalytic pyrolysis, microwave pyrolysis, etc., can be employed for the sustainable production of hydrogen. Finally, the techno-economic analysis is presented to understand the viability of pyrolysis at large scale. The outlook highlights discernments into future directions, aimed to overcome the current shortcomings.

Bioenergy and biochemicals can be sustainably produced through fermentation and anaerobic digestion (AD). However, this bioconversion processes could be more economical if the hydrolysis rates of substrates in bioreactors can be accelerated. In this review, the feasibilities of including enzymatic hydrolysis (EH) in various bioconversion systems were studied to facilitate the biological synergy. The reaction kinetics of EH in bioconversion systems comparing pretreated lignocellulosic biomass (LCB) and food waste (FW) substrates were reviewed. Possible strategies to improve the hydrolysis efficiency were explored, including co-cultivation during enzyme production and replacement of pure enzyme with on-site produced fungal mash during EH. Key insights into improvement of current AD and fermentation technologies were summarized and further formed into suggestions of future directions in techno-economic feasibility of biorefinery using mixture of the first-generation food crop feedstock with FW; and/or co-digestion of FW with LCB.

We investigated the potential application of anaerobically digested residues for generating bioenergy in the presence of alkali bifunctional material, sodium zirconate (Na2ZrO3, NZ) using a thermogravimetric analyzer connected to a mass spectrometer. Isoconversional kinetic models, compensation effect and master-plots method were used on data obtained under multiple heating rates (10, 15 and 20 °C min-1) to calculate the activation energy (Eα) and pre-exponential value (A) and reaction mechanism. The average Eα for blend samples C-DSW (NZ mixed with digested municipal solid waste (DSW)), and C-DSM (NZ mixed with digested swine manure (DSM)) were 172.24 and 171.63 kJ mol-1, which were much lower when compared to plain samples, DSW (202.51 kJ mol-1) and DSM (215.22 kJ mol-1). The total gas yields increased by 19.5 and 17.1% for NZ blended samples C-DSW and C-DSM, respectively. In addition, the hydrogen yields also increased by 79 and 44% for C-DSW and C-DSM, respectively.