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Lignocellulosic biomass dissolution in an inorganic salt hydrate (ZnCl2·4H2O) and its subsequent precipitation with water for the separation of its main compounds were investigated. For this purpose, different dissolution times and temperatures were studied, where 24 h and 70 °C were found to be the optimal choice. Three solids were obtained, which were analyzed and identified by XRD, SEM, NMR, and FTIR spectroscopy. Solid I is the undissolved part of the starting material, and it consists of lignin, which does not react with the inorganic salt hydrate and the unreacted cellulose. Solid II is a cellulose-rich solid with a low portion of hemicellulose and lignin, and Solid III is mainly pure lignin as the characterization results showed. Hemicellulose is mainly dissolved and hydrolyzed in the dissolution treatment and the amount present in all solids was very small. The reactivity of Solid I and Solid II in a hydrolysis reaction was tested (0.2 M/L H2SO4, 5 h, and 140 °C), where a significant improvement in the conversion and the yield of sugars was obtained with respect to the untreated samples in both cases. Solid II yields a large amount of total reducing sugars, with a % selectivity of 78–88%, depending on the starting biomass. [ABSTRACT FROM AUTHOR]

The experimental and theoretical analysis of the catalytic system formed by tungstic acid and its complexes with [H.sub.2][O.sub.2] and phenylphosphonic acid is reported. Hydrogen peroxide has reacted with tungstic acid to form a peroxo complex and the presence of coordinated water is corroborated by experimental spectra.

We have studied the direct synthesis of hydrogen peroxide using a catalytic system consisting of palladium supported on silica bifunctionalized with sulfonic acid groups and bromide in the absence of acid and halide promoters in solution. Catalysts with several bromide substituents were employed in the catalyst synthesis. The prepared samples were characterized by TXRF, XPS, and hydrogen peroxide decomposition. Catalysts characterization indicated the presence of only palladium (II) species in all of the samples, with similar values for surface and bulk of Pd/Br atomic ratio. The catalysts were tested via direct synthesis, and all samples were able to produce hydrogen peroxide at 313 K and 5.0 MPa. The hydrogen peroxide yield and selectivity changed with the Pd/Br ratio. A decrease in the Pd/Br ratio increases the final hydrogen peroxide concentration, and the selectivity for H2O2 reaches a maximum at a Pd/Br ratio around 0.16 and then decreases. However, the maximum hydrogen peroxide concentration and selectivity occur at slightly different Pd/Br ratios, i.e., resp. 0.4 vs. 0.16. [ABSTRACT FROM AUTHOR]

The tautomeric forms of 4,6-dimethyl-2-mercaptopyrimidine in solution were examined by infrared, ultraviolet, and nuclear magnetic resonance techniques. Density functional theory calculations elucidated these molecular structures.

This work describes a relatively simple methodology for efficiently deconstructing cellulose into monomeric glucose, which is more easily transformed into a variety of platform molecules for the production of chemicals and fuels. The approach undertaken herein first involves the dissolution of cellulose in an ionic liquid (IL), followed by a second reconstruction step aided by an antisolvent. The regenerated cellulose exhibited strong structural and morphological changes, as revealed by XRD and SEM analyses. These changes dramatically affect the hydrolytic reactivity of cellulose with dilute mineral acids. As a consequence, the glucose yield obtained from the deconstructed-reconstructed cellulose was substantially higher than that achieved through hydrolysis of the starting cellulose. Factors that affect the hydrolysis reaction include the type of cellulose substrate, the type of IL used in pretreatment, and the type of acid used in the hydrolysis step. The best results were obtained by treating cellulose with IL and using phosphotungstic acid (0.067 mol L−1) as a catalyst at 413 K. Under these conditions, the conversion of cellulose was almost complete (>99 %), with a glucose yield of 87 % after only 5 h of reaction. [ABSTRACT FROM AUTHOR]

Microalgal biomass and its cellular components are used as substrates for the production of fuels. A valuable group among the components of microalgal biomass is lipids, which act as a precursor for the production of biodiesel in the transesterification process. Some methods, including the creation of stressful conditions, are applied to increase the accumulation of lipids. This study aimed to determine the effect of limited nutrient access on the growth and development of the microalga Chlorella vulgaris and the amount of lipids stored in its cells. Aquaculture wastewater (AWW) was used in the study as a source of nutrients at doses of 20%, 40%, 60%, 80% and 100%. The amount of microalgal biomass, optical density, lipid content after extraction of the biomass in Soxhlet apparatus and chlorophyll a content were determined. It was observed that the microalgae efficiently used the nutrients contained in the AWW. The largest amount of biomass was obtained in AWW80 (727 ± 19.64 mg·L−1). The OD680 (0.492 ± 0.00) determined under the same conditions was almost five times higher in AWW than in the synthetic medium. Under nutrient-stress conditions, the content of lipids in biomass ranged from 5.75% (AWW80) to 11.81% (AWW20). The highest content of chlorophyll a in microalgal cells was obtained in AWW20 (206 ± 11.33 mg∙m−3). [ABSTRACT FROM AUTHOR]

First direct images of cobalt nanoparticles covered by a few atomic layers thick TiOxmoieties after reduction treatment of a Co/TiO2system with the simultaneous formation of Co–O–Ti bonds confirm the development of the SMSI decoration effect. [ABSTRACT FROM AUTHOR]

Recently, catalysts based on transition metal phosphides (TMPs) have attracted increasing interest for their use in hydrodeoxygenation (HDO) processes destined to synthesize biofuels (green or renewable diesel) from waste vegetable oils and fats (known as hydrotreated vegetable oils (HVO)), or from bio-oils. This fossil-free diesel product is produced completely from renewable raw materials with exceptional quality. These efficient HDO catalysts present electronic properties similar to noble metals, are cost-efficient, and are more stable and resistant to the presence of water than other classical catalytic formulations used for hydrotreatment reactions based on transition metal sulfides, but they do not require the continuous supply of a sulfide source. TMPs develop a bifunctional character (metallic and acidic) and present tunable catalytic properties related to the metal type, phosphorous-metal ratio, support nature, texture properties, and so on. Here, the recent progress in TMP-based catalysts for HDO of waste oils is reviewed. First, the use of TMPs in catalysis is addressed; then, the general aspects of green diesel (from bio-oils or from waste vegetable oils and fats) production by HDO of nonedible oil compounds are presented; and, finally, we attempt to describe the main advances in the development of catalysts based on TMPs for HDO, with an emphasis on the influence of the nature of active phases and effects of phosphorous, promoters, and preparation methods on reactivity. [ABSTRACT FROM AUTHOR]

Mesocrystals (basically nanostructures showing alignment of nanocrystals well beyond crystal size) are attracting considerable attention for modeling and optimization of functionalities. However, for surface-driven applications (heterogeneous catalysis), only those mesocrystals with excellent textural properties are expected to fulfill their potential. This is especially true for oxidative desulfuration of dibenzothiophenes (hard to desulfurize organosulfur compounds found in fossil fuels). Here, we probe the catalytic activity of anatases for the oxidative desulfuration of dibenzothiophenes under atmospheric pressure and mild temperatures. Specifically, for this study, we have taken advantage of the high stability of the (101) anatase surface to obtain a variety of uniform colloidal mesocrystals (approximately 50 nm) with adequate orientational order and good textural properties (pores around 3-4 nm and surface areas around 200 m 2 /g). Ultimately, this stability has allowed us to compare the catalytic activity of anatases that expose a high number of aligned single crystal-like surfaces while differing in controllable surface characteristics. Thus, we have established that the type of tetrahedral coordination observed in these anatase mesocrystals is not essential for oxidative desulfuration and that both elimination of sulfates and good textural properties significantly improve the catalytic activity. Furthermore, the most active mesocrystals have been used to model the catalytic reaction in three-(oil-solvent-catalyst) and two-phase (solvent-catalyst) systems. Thus, we have been able to observe that the transfer of DBT from the oil to the solvent phase partially limits the oxidative process and to estimate an apparent activation energy for the oxidative desulfuration reaction of approximately 40 kJ/mol in the two-phase system to avoid mass transfer limitations. Our results clearly establish that (101) anatase mesocrystals with excellent textural properties show adequate stability to withstand several post-treatments without losing their initial mesocrystalline character and therefore could serve as models for catalytic processes different from the one studied here., Competing Interests: The authors declare no competing financial interest.