Abstract Brazil’s beer industry has experienced a significant growth over the recent years, driving professionals to seek brewing beer focused on quality aspects. As a result of this movement, the consumer attention to products that highlight the national or local identity has rocketed in recent times, especially Brazilian types of beers, as Catharina Sour. Catharina Sour beer was produced using the traditional method to acidify the wort by lactic fermentation and using a bee pollen, as a newer source of microorganism to produce sour beers. For that, mango and passion fruit were used, including barley and wheat malt, yeast, and hop. Some physicochemical analyses were made according to EBC (European Brewery Convention) guidelines, to raise information about the process and final product. There were close correlations between the physic-chemical, sensory and liquid chromatography analysis, showing that the presence of pollen, and consequently the presence of yeast, acetic acid bacteria and fructophilic lactic acid bacteria (FLABs), can bring different aromas to Catharina Sour beers, showing an excellent potential to use this newer source of microorganisms to produce sour beers.

According to the waste-to-energy (WTE) valorization and circular economy principles, the use of waste oil and grease (WOG) for obtaining biofuels shows the tendency towards sustainability, makes the interest in green chemistry, and the development of environmentally friendly processes grow. Three different fatty wastes (from the fat trap of a sewage station, lard waste, and frying oil) were analyzed and this work showed they have no potentially toxic metals. The frying oil sample and residual lard waste showed a higher percentage of triacylglycerides resulting in higher biodiesel conversion. The samples showed physical and chemical properties (density, viscosity, and ash) within the limits established by current regulations. Bio-oil samples formed a mixture of carboxylic acids, with high acidity. However, the parameters that deviated from the maximum permitted by the standard could be adjusted blending with petroleum diesel, replacing partially the fossil energy carriers with biomass-derived energy carriers which could bring positive impacts from multiple perspectives, i.e., economic, environmental, and health.

In this work, different metal oxides containing Ti, Zr and Al were prepared and characterized and their catalytic activities for cracking, transesterification, and hydroesterification reactions of soybean oil were evaluated. It is described the synthesis of the solids by co-precipitation, and their characterization by thermogravimetry, X-ray diffraction, Brunauer-Emmet-Teller surface area determination, Fourier-transformed Raman spectroscopy, and the determination of Lewis and Brønsted acid sites by pyridine adsorption and detection through Fourier transform infrared spectroscopy (FTIR). The hydrocarbons obtained by soybean pyrolysis were analyzed by fractional distillation, acid number, FTIR, density (at 20 °C), viscosity (at 40 °C), and calculation of the cetane number. The results suggest that all of the solids exhibit catalytic activity at the second stage of the cracking reaction (deoxygenation), lowering the final acidity of the products. The solids also exhibited catalytic activity for transesterification and hydroesterification of triacylglycerides, leading to good yields in methyl fatty acid esters.

Abstract In this work, the grapheme oxide (GO) and GO/ZnO nanocomposite were successfully obtained from the oxidation of graphite and characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and thermogravimetric analysis (TGA). In the GO/ZnO nanocomposite, the GO sheets were coated with aggregated ZnO nanoneedles with ca. 20 nm of diameter. The obtained materials were used as heterogeneous catalysts for acetylation of Soybean Fatty Acids Methyl Esters (FAME), promoting the epoxy ring-opening using acetic anhydride. The epoxy ring was almost completely opened in the presence of GO or GO/ZnO nanocomposites, with conversion rates up to 99% and selectivity of ca. 90%, and partially opened using only ZnO. The GO/Zn and GO catalysts were reused three times with conversion rates of ca. 85 and 74%, respectively.

Biodiesel demand is increasing all over the world and the inhibition of microbial growth during the storage of this biofuel is extremely important. There are few studies involving the evaluation of biocides specifically for biodiesel. In the present work, we synthesized and evaluated a set of biocide candidates from chemical transformations in triacylglycerides. Samples of pure biodiesel with the products were evaluated against microorganisms which have been isolated from biodiesel/diesel blends (fungi A. niger, A. fumigatus, C. albicans and S. cerevisiae; and bacteria B. subtilis and Acinetobacter sp.). None of the products inhibited the growth of bacteria. Four nitrated derivatives presented fungicidal activity. The nitrated derivatives were also evaluated as cetane number improvers for B7 biodiesel/diesel blend. The nitrates of soybean methoxylated ethylene glycol esters increased the cetane number by more than three points. Despite showing modest biocide activity, the results can guide the planning of new products from triacylglycerides.

A great diversity of fruits is used in the food industry to obtain different products such as juices, sauces and foods. However, the food industry produces high amounts of residues. Passion fruit and guava are worldwide known fruits and very used by the food industry and generate tons of seed as residue. This work aims to study the extraction of oils from passion fruit and guava juice industries residues, their characterization and potential application as raw materials to obtain biodiesel and bio-oil. The passion fruit and guava seed oils content were 25 and 9%, respectively. In both oils, polyunsaturated fatty acids are predominant. Biodiesel obtained by esterification/transesterification of both seed oils match most of the parameters specified for biodiesel in Brazil. Bio-oils obtained by thermal cracking of the seed oils were mainly composed by hydrocarbons similar to those observed in petroleum diesel.

In the last decade, the research works on microbial as a potential source of lipid for biodiesel production have been growing. In this work, the potential of a sludge from high-rate lagoons in urban sewage treatment, composed mainly by Chlorella sp., as oil source for biodiesel production, was studied. The potential of Chlorella sp. growth in photobioreactor under controlled conditions was also investigated. Low lipid content (up to 3%) was observed in both cases. The composition of both oils showed high amount of fatty acids and fatty acid based compounds, however there are also other non-fatty acid based lipids. Density and viscosity of biodiesel from biosolid oil were determined and the results showed that these physico-chemical properties do not match the specification required for biodiesel. The results showed that sewage sludge from Samambaia treatment station (DF, Brazil) and Chlorella sp. cultivated under the conditions described in this work are not potential sources of fatty material for biodiesel production.

This work shows the modification of microcrystalline cellulose by the selective oxidation of primary hydroxyl groups to carboxylate groups by a 2,2,6,6-tetramethylpiperidine-1-oxyl radical (TEMPO)-mediated system and its application as a heterogeneous ligand by ionic exchange with catalytic metals ions such as palladium, nickel and copper. Afterwards is described the application of the synthesized material as catalyst in coupling reactions such as Suzuki-Miyaura coupling and C−O bond formation reaction in different conditions, which are of great importance for the synthesis of drugs, natural products and new materials such as dendrimers, liquid crystals and polymers with magnetic and optical properties. The carboxyl cellulose matrix shows to have superior catalytic results as a ligand for all coupling reactions. Can be also highlighted the affinity of the carboxyl cellulose ligand in polar solvents such as water and alcohols and its application in mild conditions.

In this work, we compared 1.40 T nuclear magnetic resonance (NMR) to 7.05 T (60 and 300 MHz for proton, respectively), and mid-infrared with attenuated total reflectance (FTIR-ATR), associated with chemometrics methods, for the quantification of the reaction yield during esterification of fatty acids with methanol. The results showed that the integrated intensities of the ester C=O stretching region, relative to the total C=O stretching region, is useful to quantify the fatty acid methyl ester (FAME) concentration. Comparing the results obtained by the different final models: NMR (1.40 T and 7.05 T), FTIR-ATR using multivariate partial last squares regression (PLS) with orthogonal signal correction (OSC), and univariate ordinary least squares (OLS), the NMR of 1.40 T (60 MHz for proton) showed more advantages when compared to a high field spectrometer, due to the non-use of cryogenic and solvents and less laborious work for obtaining results.

Due to its low cost, formaldehyde was commonly used as conservative in hygienic and cosmetic products. However, formaldehyde is strongly reactive and toxic, so its use has been forbidden in several products. Recently, it was reported by different media that formaldehyde has been added illegally in milk, causing innumerous health problems. In this work we developed a colorimetric indicator paper based on Schiff 's reagent, which can be associated with a smartphone application. It was observed that the paper stabilizes the Schiff 's reagent, avoiding its decomposition during short periods. It was also possible to successfully detect the presence of formaldehyde in commercial products, such as: detergents, shampoos and conditioners. Regarding milk based products, the indicator paper is very sensitive to detect formaldehyde, having a sensibility of 0.01% (v/v). The developed indicator paper has low cost and can help the supervision of milk products, as a trial test. Also it is possible to commercialize this product to common consumer, due to its simplicity.

The Coordination for the Improvement of High Education Personnel (CAPES), the Brazilian federal agency for graduate programs, plays a fundamental role for the expansion and consolidation of the National Postgraduate System (SNPG) and the execution of the National Graduate Plan (PNPG) 2011-2020. In this paper, we discuss the evolution of the Brazilian graduate program in chemistry and its role in the formation of highly qualified professionals in chemistry (academic master’s degree, professional master’s degree and doctoral degree) for the academy, teachers and lecturers for all levels of the education system, as well for the non-academic market.

A biphasic catalytic system based in the ionic liquid 1-butyl-3-methylimidazolium hexafluorophosphate was employed for tandem hydroformylation-amine condensation reactions of soybean FAME using HRhCO(PPh3)3 as the catalyst precursor and n-butylamine. Using a tenfold excess of the ligand PPh3, the presence of the ionic liquid increased the selectivity for imine if compared to the reaction carried out under similar conditions, but in homogeneous media.The yield for imine reached 75% after 24 h. On the other hand, in the absence of a PPh3 excess, the effect of using the ionic liquid was opposite and the selectivity for imine decreased. This supposedly occurred due to the generation ofN-heterocyclics carbenes, which would coordinate to Rh to form species active for parallel and/or consecutive reactions. When an excess PPh3 is used, it suppress the carbenes coordination, maintaining the Rh complex in a form active for hydroformylation.The obtained imine products presented remarkable antimicrobial activity towards a set of fungi and bacteria commonly present in fuel storage tanks.

A colorimetric kit for methanol detection in ethanol-containing fuels and ease of use in the field was developed and tested. The analysis can detect the presence of methanol in fuels when exceeding specification (0.5% v/v) in about 20 min and its simple instrumentation does not require a specialist. The kit method was successfully validated at gas stations located in São Paulo State and the Federal District.

Nanopartículas magnéticas compostas por óxidos mistos de ferro/cádmio (ICdO) e ferro/ estanho (ISnO) foram usadas como catalisadores em reações relevantes para diferentes tecnologias de produção de biodiesel. Estes compostos foram ativos para hidrólise e transesterificação de óleo de soja, bem como para a esterificação de ácidos graxos obtidos a partir do óleo de soja. Na esterificação mediada por ISnO foram alcançados altos rendimentos, ca. 84%, após 1 h de reação a 200 ºC. O óxido foi recuperado magneticamente e reutilizado quatro vezes sem perda da sua atividade catalítica, enquanto que uma perda significativa foi observada quando ICdO foi usado. ISnO demonstrou também atividade para a produção de biodiesel a partir de óleo de macaúba, um substrato altamente ácido.

Magnetic mixed iron/cadmium (ICdO) and iron/tin (ISnO) oxide nanoparticles were used as catalysts in relevant reactions for biodiesel production technologies. These compounds were active for hydrolysis and transesterification of soybean oil as well as esterification of soybean oil fatty acids. In the esterification assisted by ISnO high yields, ca. 84%, were achieved, after 1 h reaction at 200 ºC. The oxide was magnetically recovered and reused four times without loss in its activity, while a loss of activity was observed for ICdO catalyst. ISnO also demonstrated catalytic activity for macauba oil, a highly acidic substrate.

Neste trabalho descrevemos a obtenção de hidrocarbonetos líquidos por meio do hidrocraqueamento catalítico de óleo de soja, dendê e mamona, na presença e ausência de catalisadores nanoparticulados de rutênio e ródio. A reação realizada a 200 ºC leva somente à hidrogenação de ligações duplas C=C. No entanto, a 400 ºC, foi observada a decomposição dos triacilglicerídeos, levando a hidrocarbonetos e compostos oxigenados. O hidrocraqueamento catalítico de óleos vegetais na presença de Rh e Ru levou a um aumento da quantidade de produtos desoxigenados e à formação de hidrocarbonetos lineares de cadeia longa, que são adequados para utilização como combustível para motores diesel, quando comparado com o da reação de pirólise na ausência de catalisadores. O catalisador de Ru é mais eficaz do que o catalisador de Rh, especialmente no caso do óleo de mamona, provavelmente devido à sua maior oxofilicidade quando comparado com Rh.

We describe herein the production of liquid hydrocarbons through the catalytic hydrocracking of soybean, palm tree and castor oils, in the presence and absence of ruthenium and rhodium nanoparticle catalysts. The reaction at 200 ºC leads to the hydrogenation of C=C double bonds only. However, at 400 ºC, the decomposition of the triacylglycerides was observed, leading to hydrocarbons and oxygenated compounds. The catalyzed hydrocracking of vegetable oils in the presence of Rh and Ru strongly increased the amount of deoxygenated products and the formation of long-chain linear hydrocarbons, which are suitable for use as diesel fuel, when compared with pyrolysis reaction in the absence of the catalysts. The Ru catalyst is more effective than Rh, especially in the case of castor oil, probably due to its higher oxophilicity when compared to Rh.