The hydrogenation of muconic acid (MA) to bio-adipic acid (AdA) is one of the green chemical processes that has attracted the most interest in recent years. Indeed, MA can be readily obtained from biomass through fermentative processes. Here, we aimed to investigate the synergic effect of electronic promotion that the addition of a second metal, even in small quantities, can have on Pd-based catalyst, known for its low stability. Ni and Zn were taken into consideration and two different catalysts (1%Pd₈Ni₂/HHT and 1%Pd₈Zn₂/HHT) were synthetized by sol immobilization method and supported on high-temperature, heat-treated carbon nanofibers (HHT-CNFs) that are known to enhance the stability of palladium. The catalysts were tested in MA hydrogenation and thoroughly characterized by TEM, ICP, and XPS analysis to unveil the effect of the second metal. To solve the solubility issue and have a starting material as similar as feasible to the post-fermentation conditions of the biomass, sodium muconate salt was chosen as a substrate for the reaction. All of the synthetized bimetallic catalysts showed a higher activity than monometallic Pd and better stability during the recycling tests, pointing out that even a small amount of these two metals can increase the catalytic properties of monometallic Pd.

The need to replace conventional fuels with renewable sources is a great challenge for the science community. H₂ is a promising alternative due to its high energy density and availability. H₂ generation from formic acid (FA) decomposition occurred in a batch and a packed-bed flow reactor, in mild conditions, using a 2% Pd₆Zn₄/HHT (high heated treated) catalyst synthesised via the sol-immobilisation method. Experimental and theoretical studies took place, and the results showed that in the batch system, the conversion was enhanced with increasing reaction temperature, while in the continuous flow system, the conversion was found to decrease due to the deactivation of the catalyst resulting from the generation of the poisoning CO. Computational fluid dynamics (CFD) studies were developed to predict the conversion profiles, which demonstrated great validation with the experimental results. The model can accurately predict the decomposition of FA as well as the deactivation that occurs in the continuous flow system. Of significance was the performance of the packed-bed flow reactor, which showed improved FA conversion in comparison to the batch reactor, potentially leading to the utilisation of continuous flow systems for future fuel cell applications for on-site H₂ production.

The liquid-phase hydrogenation of muconic acid (MA) to produce bio-adipic acid (AdA) is a prominent environmentally friendly chemical process, that can be achieved through two distinct methodologies: catalytic direct hydrogenation using molecular hydrogen (H₂), or catalytic transfer hydrogenation utilizing a hydrogen donor. In this study, both approaches were explored, with formic acid (FA) selected as the hydrogen source for the latter method. Palladium-based catalysts were chosen for these processes. Metal’s nanoparticles (NPs) were supported on high-temperature heat-treated carbon nanofibers (HHT-CNFs) due to their known ability to enhance the stability of this metal catalyst. To assess the impact of support functionalization on catalyst stability, the HHT-CNFs were further functionalized with phosphorus and oxygen to obtain HHT-P and HHT-O, respectively. In the hydrogenation reaction, catalysts supported on functionalized supports exhibited higher catalytic activity and stability compared to Pd/HHT, reaching an AdA yield of about 80% in less than 2 h in batch reactor. The hydrogen-transfer process also yielded promising results, particularly with the 1%Pd/HHT-P catalyst. This work highlights the efficacy of support functionalization in improving catalyst performance, particularly when formic acid is used as a safer and more cost-effective hydrogen donor in the hydrogen-transfer process.