Dra. Azócar-Ulloa, Laura

The production of fatty acid methyl esters (FAME) from waste frying oil (WFO) was studied using fly ash as received as a heterogeneous catalyst. The fly ash used in this research had a high content of both CaO and SO3, two compounds that have been previously proposed as catalysts in FAME production. The study was carried out on the basis of a response surface methodology (RSM). The model generated by RSM predicted as optimal conditions to obtain a 100% FAME yield at a methanol-to-oil molar ratio of 3.1:1, 11.2 (wt.% based on oil weight) fly ash and a temperature of 59 C with agitation at 245 rpm and 6 h of reaction time. Additional experiments comparing anhydrous with aqueous medium showed that fly ash presented a high catalytic capacity to transform free fatty acids (FFA) into FAME through consecutive hydrolysis and esterification processes (hydroesterification) compared with that associated with the transesterification mechanism. According to the results, the fly ash used in this study would act as a multipurpose or “versatile” catalyst due to its chemical composition with constituents that act as acidic and basic catalysts, therefore, catalyzing the transesterification and hydroesterification reactions simultaneously and increasing the conversion yields of FAME.

The catalytic oxidation of phenethoxybenzene as a lignin model compound with a β-O-4 bond was conducted using the Keggin-type polyoxometalate nanocatalyst (TBA)5[PMo10V2O40]. The optimization of the process’s operational conditions was carried out using response surface methodology. The statistically significant variables in the process were determined using a fractional factorial design. Based on this selection, a central circumscribed composite experimental design was used to maximize the phenethoxybenzene conversion, varying temperature, reaction time, and catalyst load. The optimal conditions that maximized the phenethoxybenzene conversion were 137 ◦C, 3.5 h, and 200 mg of catalyst. In addition, under the optimized conditions, the Kraft lignin catalytic depolymerization was carried out to validate the effectiveness of the process. The depolymerization degree was assessed by gel permeation chromatography from which a significant decrease in the molar mass distribution Mw from 7.34 kDa to 1.97 kDa and a reduction in the polydispersity index PDI from 6 to 3 were observed. Furthermore, the successful cleavage of the β-O-4 bond in the Kraft lignin was verified by gas chromatography–mass spectrometry analysis of the reaction products. These results offer a sustainable alternative to efficiently converting lignin into valuable products

A series of tetrabutyl ammonium (TBA) salts of V-included Keggin-type polyoxoanions with W (TBA4PW11V1O40 and TBA5PW10V2O40) and Mo (TBA4PMo11V1O40 and TBA5PMo10V2O40) as addenda atoms were prepared using a hydrothermal method. These synthesized materials were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), UV-Vis diffuse reflectance (DRS UV-Vis), thermogravimetric analysis (TGA), CHN elemental analysis (EA), inductively coupled plasma spectrometry (ICP-MS), and N2 physisorption techniques to assess their physicochemical/textural properties and correlate them with their catalytic performances. According to FT-IR and DRS UV-Vis, (PVXW(Mo)12−XO40)(3+X)− anions are the main species present in the TBA salts. Additionally, CHN-EA and ICP-MS revealed that the desired stoichiometry was obtained. Their catalytic activities in the liquid-phase aerobic oxidation of benzyl alcohol to benzaldehyde were studied at 5 bar of O2 at 170 °C. Independently of the addenda atom nature, the catalytic activity increased with the number of V in the Keggin anion structure. For both series of catalysts, TBA salts of polyoxometalates with the highest V-substitution degree (TBA5PMo10V2O40 and TBA5PW10V2O40) showed higher activity. The maximum benzyl alcohol conversions obtained were 93% and 97% using (TBA)5PMo10V2O40 and (TBA)5PW10V2O40 as catalysts, respectively. In all the cases, the selectivity toward benzaldehyde was higher than 99%.

Nowadays, leaves, bark, and branches are generated from the tree-pruning process in urban places, where their management is a problem because of the necessity of disposal. These wastes are lignocellulosic biomasses with poor properties for use in biofuel production, but with interesting projections for building block products such as phenol compounds. Therefore, extensive biomass characterization of urban pruning from Liquidambar styraciflua L. was developed to evaluate its composition as a tool for phenol production through thermal processing, in which solvent extraction is a complementary tool for selectivity improvement. The results showed high lignin content in bark and leaves at 45 and 28 %, respectively, compared with that in branches (14 %). Additionally, high extractives in leaves (14 %) could be an additional source of phenols. The lignin units were analyzed by Raman dispersion, revealing p–hydroxyphenyl (H) units in the bark, guaiacyl (G) units in the bark and leaves, and syringyl (S) units only in the branches. Furthermore, the micropyrolysis coupled with gas chromatography/mass spectrometry assay realized at 600 ◦C showed high presence of phenolic compounds in the three biomass investigated, where a high phenol concentration was identified in leaves, probably due to the S unit degradation during pyrolysis. With these results, an assay for bio-oil production was performed in a low-temperature pyrolysis reactor using leaves as feedstock, reaching a low bio-oil yield with high water content favored for the high inorganic content of leaves (13 %). The produced bio-oil was used for liquid–liquid extraction evaluation, where 1-octanol and methyl isobutyl ketone were identified as interesting solvents for catechol and phenol extraction, respectively. This article presents the challenge of characterizing each part of urban trees, which could be a tool to promote the use of urban pruning by studying the thermal degradation mechanism to implement processes for high-value products, such as phenols produced from L. styraciflua L.