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In recent years, algae have emerged as a promising feedstock for biofuel production, due to their eco-friendly, sustainable, and renewable nature. Various methods, including chemical, biochemical, and thermochemical processes, are used to convert algal biomass into biofuels. Pyrolysis, a widely recognized thermochemical technique, involves high temperature and pressure to generate biochar and bio-oil from diverse algal sources. Various pyrolytic processes transform algal biomass into biochar and bio-oil, including low pyrolysis, fast pyrolysis, catalytic pyrolysis, microwave-assisted pyrolysis, and hydropyrolysis. These methods are utilized to convert a range of microalgae and cyanobacteria into biochar and bio-oil. In this publication, we will discuss catalytic pyrolysis using mesoporous materials, such as SBA-15. Mesoporous catalysts have earned significant attention for catalytic reactions, due to their high surface area, facilitating the better distribution of impregnated metal. Pyrolysis conducted in the presence of a mesoporous catalyst is viewed more as efficient, compared to reactions occurring within the smaller microporous cavities of traditional zeolites. SBA-15 supports with incorporated Zr and/or Ce were synthesized using the direct hydrothermal synthesis method. The catalyst was characterized using structural and morphological technical analysis and utilized for the pyrolysis reaction of the algal biomass. [ABSTRACT FROM AUTHOR]

Photocatalytic coatings are difficult to obtain on textile materials because of the sometimes contradictory properties that must be achieved. In order to obtain a high efficiency of a photocatalytic effect, the metal–oxide semiconductor must be found in the vicinity of the coating–air interface in order to come into direct contact with the contaminant species and allow light radiation access to its surface. Another necessary condition is related to the properties of the covering textile material as well as to the stability of the xerogel films to light and wet treatments. In this sense, we proposed a solution based on hybrid silica films generated by sol–gel processes, coatings that contain as a photocatalyst TiO2 sensitized with tetracarboxylic acid of iron (III) phthalocyanine (FeTCPc). The coatings were made by the pad–dry–cure process, using in the composition a bifunctional anchoring agent (3-glycidoxipropyltrimethoxysilane, GLYMO), a crosslinking agent (sodium tetraborate, BORAX), and a catalyst (N-methylimidazole, MIM) for the polymerization of epoxy groups. The photodegradation experiments performed on methylene blue (MB), utilized as a model contaminant, using LED or xenon arc as light sources, showed that the treatment with BORAX improves the resistance of the coatings to wet treatments but worsens their photocatalytic performances. [ABSTRACT FROM AUTHOR]

The study presents the results regarding the photocatalytic behavior of some water-based styrene-acrylic coatings containing TiO2 nanoparticles sensitized with metal-phthalocyanine tetracarboxylic acids. Coating materials have been studied in terms of color characteristics, photocatalytic behavior, and resistance to self-degradation depending on the structure of phthalocyanine sensitizers. Coatings that were exposed to Xenon light showed degradation of the organic sensitizer rather than of the binder. Photocatalytic tests using methylene blue as a standard contaminant indicated that the coating containing TiO2 nanoparticles sensitized with Fe(III) phthalocyanine tetracarboxylic acids showed the highest efficiency both in ultraviolet or visible light. In this case, the UV light induced a photodegradation rate that was greatly increased of about fifty times comparatively with that induced by LED light and was determined by two different mechanisms, but side reactions like methylene blue and sensitizer self destruction are possible to occur simultaneously. Photocatalytic materials of this type are suitable to be used as decorative coatings especially for indoor applications. [ABSTRACT FROM AUTHOR]