The reduction of oil resources and the consequent increasing price of oil distillates as well as the environmental concerns of conventional fuels has renewed and increased interest on the preparation of biofuels from renewable resources. One of those interests is nowadays focused on biodiesel, which is usually prepared from crude and refined triglyceride containing raw materials, such as vegetable oils, animal fats and wastes—for instance waste cooking oil and yellow and brown grease. Since several commercial interests converge on this kind of feedstock, one of the priorities being crops for human food supply, the research efforts on biodiesel production are diverting towards the use of low quality triglyceride-containing raw materials. Nevertheless, all of these feedstocks feature high water and free fatty acids (FFAs) content, which strongly affects the behaviour of conventional homogeneous base catalysts. These catalysts are primarily NaOH and KOH, but also NaOCH₃ and KOCH₃ are employed—as solutions in methanol—mainly in large-scale production plants. In this context, an appropriate solid acid catalyst which could simultaneously carry out esterification of FFAs and transesterification of triglycerides would be of great interest for biodiesel production. Moreover, a heterogeneous acid catalyst could be easily incorporated into a packed bed continuous flow reactor, simplifying product separation and purification and reducing waste generation. The present review attempts to provide a wide overview on the possibility of heterogeneous acid catalysts for biodiesel production replacing the homogeneous conventional process. In this way, three aspects of solid acid catalysis for biodiesel production will be reviewed. The first section deals with the solid acid-catalyzed esterification of FFAs, the second topic relates to the transesterification of triglycerides, while the third deals with solid acid-catalyzed transformation of bioglycerol into oxygenated compounds for biodiesel formulation.

Within the present contribution we highlight the feasibility of standard refinery units for the production of biofuels from different biomass-derived feedstock. The energy densification of biomass, as well as it’s logistics and incorporation within the refinery supply chain is thoroughly discussed. Likewise, special attention is focused on the catalytic cracking and hydrotreating of triglyceride-rich biomass feedstock, which is probably the most suitable one for co-processing in conventional refinery conversion units. However, the opportunities of other highly oxygenated feedstocks such as pyrolysis oils and sugars are also discussed. Conversion of different feedstocks into conventional liquid fuels by coupling of aqueous phase reforming (APR) with catalytic systems typical of standard petroleum refineries is also evaluated. Thus, here we review the chemistry, catalysis and challenges involved in the production of biofuels from biomass in conventional refineries.

This review revises the advances in the chemocatalytic processes for producing renewable carboxylic acids for the synthesis of bio-based polymers and proposes the actions to overcome the problems threatening their technical and economic viability.

This article reviews the recent advances in the development of zeolite catalysts for biomass valorization processes to produce both biofuels and/or bio-based chemicals, which is an emerging and fast expanding field. The work deals with different types of feedstocks, including vegetable oils, lignocellulose and sugars, as well as with a number of relevant intermediates and platform molecules. Transformation of biomass into valuable products is hindered by a number of factors, mainly related to its complex composition, as biomass typically consists of bulky molecules with high oxygen content. Accordingly, biomass processing usually requires the combination of multiple steps and severe conditions, hence concepts like atom efficiency, product selectivity, and catalyst deactivation become of special relevance. A great progress has been achieved in the past years engineering the properties of zeolites for being adapted to the challenges associated to biomass valorization. The possibility of tailoring the main physicochemical properties of zeolites has become now a reality, being the major reason that explains the success achieved by this class of materials in a growing variety of biomass conversion pathways, as those described in this work: catalytic cracking and pyrolysis, hydrotreatments, with special relevance for hydrodeoxygenation processes, as well as in a high number of condensation, isomerization, and dehydration reactions. Thus, the development of hierarchical zeolites, exhibiting enhanced accessibility, and the possibility of introducing and combining in a controlled way different types of active sites (Brønsted and Lewis acid centers, basic sites, and metal phases) are the main basis of the excellent performance of zeolites in numerous biomass conversion routes.