Carbonyl compounds (CC) can be formed during the craft beer production process, which influence the sensory properties, in addition to their toxicity. The formation of bound CC, in craft beers, is favored by the high reactivity of these substances. This work aimed to quantify 15 carbonyl compounds, in free and bound forms, in craft beers using hydrolysis (bound CC only) and derivatization reactions. Acetaldehyde concentrations ranged from 8.83 to 466.1 µg L-1 (free fraction) and 22.47 to 1665 µg L-1 (bound fraction). Other compounds found were acrolein (free + boundmax.: 2897 µg L-1), benzaldehyde (free + boundmax.: 1326 µg L-1), heptanal (free + boundmax.: 1140 µg L-1) and formaldehyde (free + boundmax.: 97.73 µg L-1). Craft beers showed a proportion of up to 76% for CC in the bound form, which can be related to undesirable flavors in beverages. The consumption of craft beers containing freeand bound-CC (especially acrolein) could pose a risk to the health of frequent consumers. (CC process properties toxicity substances 1 forms only reactions 883 8 83 8.8 4661 466 466. L1 L L- fraction 2247 22 47 22.4 166 fraction. . boundmax. boundmax 289 L1, , 132 114 9773 97 73 97.7 L1. 76 form beverages boundCC especially consumers 88 8. 46 224 2 4 22. 16 28 13 11 977 9 7 97.

This study indicates the use of Phallusia nigra as a potential biomonitor of mercury contamination. In this way, Hg levels were measured in seawater and different parts of ascidians (tunic, hepatopancreas, and branchial basket) from eight different sites in the Todos os Santos Bay, Salvador-Bahia. The ascidians were lyophilized, weighed, and taken to the DMA-80 (direct mercury analyzer); the method accuracy was confirmed by analyzing the certified material DORM 4 muscle tissue and MEES-3 marine sediment with a confidence level of 95%. The results were evaluated through the Tukey’s test and it was possible to observe a higher concentration of Hg (82.00 312.7 ng g-1) in the branchial basket, followed by the hepatopancreas (69.67 130.7 ng g-1) and tunic (21.63-33.27 ng g-1). Thus, the branchial basket was the only tissue capable of identifying spatial differences in pollution between the points. contamination way tunic, (tunic Bay SalvadorBahia. SalvadorBahia Salvador Bahia. Bahia Salvador-Bahia lyophilized weighed DMA80 DMA 80 DMA-8 direct analyzer analyzer) MEES3 MEES 3 MEES- 95 95% Tukeys Tukey s 82.00 8200 82 00 (82.0 3127 312 7 312. g1 g 1 g-1 69.67 6967 69 67 (69.6 1307 130 130. 21.6333.27 21633327 21.63 33.27 21 63 33 27 (21.63-33.2 g1. . Thus points DMA8 8 DMA- 9 82.0 820 0 (82. 31 g- 69.6 696 6 (69. 13 6333 21.6333.2 2163332 2163 21.6 3327 33.2 2 (21.63-33. 82. (82 69. (69 633 21.6333. 216333 216 21. 332 33. (21.63-33 (8 (6 21.6333 21633 (21.63-3 ( 21.633 (21.63- (21.63 (21.6 (21. (21 (2

Circular chemistry (CC) is an approach for establishing chemical processes to become truly circular and sustainable. It adopts the principles of circular economy (CE), employing life cycle approaches and systems thinking, which help to understand and address the sustainability issues of chemical processes and products. Within this whole context, it is possible to identify some problems of the current lifestyle, such as plastic waste disposal, CO2 emission, e-waste, among others, which need to be addressed accordingly. The reuse provided, well-structured within the context of circular chemistry, can bring benefits in all spheres: social, environmental and economic. Thus, the purpose of this revision is to present CE and CC as the pillars for a sustainable development, bringing discussions about: CE and CC systems; sustainable chemistry; and chemistry 4.0, which embeds digitization, sustainability, and circular economy in industrial chemical processes. Through the knowledge of chemistry, both CC and CE can contribute with innovative methods and processes which maximize benefits, eliminating, or, at least, reducing adverse impacts, thus contributing to construct a mutually beneficial relationship between science and society, its surroundings, and the environment. Therefore, implementing this new model is an opportunity that challenges the human imagination in building a better world.

Green hydrogen is a fuel capable of promoting sustainable energy development and is gaining attention in the current global energy transition framework. The global shift toward decarbonization has triggered a substantial boost in the hydrogen industry. This study presents an overview of the current status of hydrogen production, regulation of the green hydrogen segment, hydrogen storage, distribution, and transportation, and final use and application. We also critically discuss the viability of adopting green hydrogen in terms of possible economic and environmental impacts as well as the main challenges and opportunities it represents for the Chemical Sciences.

The crescent number of scientific articles published per year shows that research on biodiesel continues to play an important role to support the growing demand for this biofuel. The second edition of Biodiesel: An Overview presents the worldwide research in the last 15 years. Microalgae biomass is the most studied raw material alternative in this period and several studies have been carried out to develop basic heterogeneous catalysts for biodiesel production. Concerning to production technologies, supercritical conditions and intensification process have been extensively investigated. The development of new antioxidants additives has focused mainly on biomass-derived formulations and there are few studies on biocide candidates. In terms of pollutant emissions, in general, the studies showed that the addition of biodiesel generates lower concentrations of polycyclic aromatic hydrocarbons (PAH), CO and n-alkanes pollutants, but carbonyl compounds, major ions and NOx are emitted in a higher concentration compared to pure diesel.

The study of quality indicators in the process of obtaining ozonized vegetable oils is useful for monitoring the ozonation reaction. The Brazilian oils “dendê”, soy, corn, rice and sunflower were studied, all of them were ozonated applying different doses of ozone. Ozonized oils were evaluated by determining the physicochemical indexes of peroxide, acidity, iodine and density in addition viscosity, fatty acid composition and microbiological activity were determined. The results showed that of the five ozonized oils evaluated, “dendê” oil exhibited a higher peroxide index, approximately 1746 mmol-equiv kg-1, using an applied ozone dose of 97 mg g-1, during an hour and a half of the ozonation reaction. This result could be explained by its chemical composition, rich in oleic acid that facilitates the reaction with ozone due to its spatial conformation. It was also demonstrated that “dendê” oil exhibits a greater antibacterial activity with minimum inhibitory concentration (MIC) values ranging from 1.9 to 4.75 mg mL-1 against Staphylococcus aureus, Pseudomonas aeruginosa and Escherichia coli. It is suggested that the ozonated “dendê” oil presents greater possibilities to be used in the preparation of pharmaceutical or cosmetic formulations.

A new analytical protocol has been developed for the determination of mercury in surface sediments using dithiothreitol (DTT) as a new chelating reagent for the extraction. This protocol requires a small sample mass (250 mg), 4.0 mL of a 0.1 M (pH = 9.0) aqueous DTT solution, and sonication for 30 min, followed by cold vapor atomic fluorescence spectrometry (CV-AFS). The limits of detection and quantification determined were 6 and 18 ng g−1, respectively. The method was validated using three standard reference materials, SRM NIST 1646a, PACS-2, and MESS-3, with recoveries in the range of 102-124%. The new analytical protocol was successfully applied in riverine surface sediments, revealing concentrations in the range of 220-340 ng g−1. The results obtained by CV-AFS were compared to those obtained by DMA-80 (direct mercury analyzer). The linear regression equation obtained was [CV-AFS] = (0.91 ± 0.07)[DMA-80] + (0.04 ± 0.02), revealing no systematic difference between the analytical methods. Hence, the proposed method does not require the complete digestion of the sediment, and was found to be comprehensive, simple, accurate and suitable to be employed for determination of mercury in sediment samples.

In 2002, the Brazilian Chemical Society have promoted several activities aiming to prepare a document to discuss the education in Chemistry in Brazil, the new model of research funding, the area situation and its perspectives. The document drew up diagnoses and brought up proposals that were organized into six mobilizing axes. Among its conclusions it was expected an alignment of scientific and technological research, considering the central role of Chemistry in solving problems and overcoming challenges affecting the education, full citizenship, climate changes, food production and quality, access to and quality of water, energy security, preservation of ecosystems and species, emerging diseases and quality of life. The current moment brings again challenges, imposed by a new technological generation, the transformations of the urban societies and by the commitment with a sustainable development. This article seeks to outline a panorama, using as background the Industry 4.0, the Society 5.0, the Sustainable Development Objectives, the creation of the EMBRAPII, the SENAI Institutes of Innovation and the role of the graduate programs in Chemistry, in order to construct a new agenda under the scope of the SBQ for the next 15 years.

In this work, the redox activity of fine diesel/biodiesel particulate matter (PM2.5) was studied in order to approach its toxicity from reactive oxygen species, due to adverse effects it may cause to human health. The oxidative potential was measured by the dithiothreitol (DTT) assay in order to study the relative contribution of water-soluble transition metals, polycyclic aromatic compounds (PAH), nitro-PAH, and quinones. It was analyzed a total of 24 samples collected from primarily diesel/biodiesel-exhausted particles from buses. The rate concentrations of PM2.5 redox activity ranged 0.020-0.069 nmol min-1 μg-1, with median at 0.040 nmol min-1 μg-1 (on average, 0.042 ± 0.005 nmol min-1 μg-1 for morning, 0.033 ± 0.007 nmol min-1 μg-1 for afternoon and 0.045 ± 0.009 nmol min-1 μg-1 for night). The transition metals appear to dominate the DTT response, since they were responsible up to 89% of redox activity measured in the samples. Apparently, the metal fraction contained in PM2.5 demonstrated a greater ability to catalyze reactions that promote the formation of reactive oxygen species when compared to organic compounds. It was observed that the oxidative potential of PM2.5 particles emitted from diesel/biodiesel (B7) is similar to diesel-emitted particles.

In this study, it is reported the fractal dimension and morphology of ultrafine particles emitted by a diesel engine run with B4, B50, and B100. Transmission electron micrographs evidenced two main groups of particles with characteristic and distinct morphological behaviors: (i) particle agglomerate structures self-organized within a fractal-like geometry, and (ii) amorphous and irregular particles with diffuse edges in a liquid-like particle appearance, mainly associated with some sub-fractions of samples collected from B50 and B100 combustion. Particles from (i) showed typical diesel soot morphology and fractal dimension. Primary particle diameter (Dpp) was 24 ± 4 nm, 23 ± 4 nm, and 20 ± 4 nm for B4, B50, and B100, respectively. Mean aggregate gyration diameters (Dg) ranged from 242 ± 140 nm for B4, 210 ± 135 nm for B50, and to 232 ± 140 nm for B100. In turn, fractal dimensions (Df) were 1.94, 1.89, and 1.99 for B4, B50, and B100, respectively. On the other hand, particle from (ii) had their morphology impaired from the addition of biodiesel to petrodiesel in a way it did not follow a fractal geometry.

This paper deals with the solubility and reactivity of gases, especially in water, covering the main aspects that influence the dissolution process, namely polarizability of atoms or molecules in gas phase and their ability to react with the solvent. The discussion highlights the importance of solubility of gases in several biological processes, such as respiration and photosynthesis, hydrogen storage and industrial processes, as the production of carbonated beverages. The discussion also addresses the importance of gas solubility in atmospheric chemistry and aquatic environments.

Quinones are a group of semi-volatile organic substances, ubiquitous in nature, belonging to the class of oxygenated polycyclic aromatic hydrocarbons (Oxygenated PAH). These compounds are formed in biogenic processes, through the oxidative metabolism of endogenous compounds, such as catecholamines, estrogen hormones and xenobiotics, as well as directly emitted to the atmosphere, through the incomplete combustion of organic matter, especially the fossil fuels. Additionally, the quinones are formed in the atmosphere by photooxidation of Polycyclic Aromatic Hydrocarbons (PAH). Their reduction products (semiquinones and hydroquinones) are of toxicological interest, due to their ability in generate reactive oxygen species, which may cause damage to membranes, proteins and DNA and, among others damages, may lead to carcinogenesis and induce apoptosis. The most frequently used analytical methods for quantification of quinones in the atmosphere, either in its original form or as derivatized compounds, are high-performance liquid chromatography coupled to mass spectrometry (HPLC-MS) and gas chromatography coupled to mass spectrometry (GC-MS). This review aims to highlight the chemical properties of 1,2-naphthoquinone, 1,4-naphthoquinone, 1,4-benzoquinone, 9,10-phenanthraquinone and 9,10-anthraquinone, the more volatile, reactive and abundant quinones in the atmosphere, as well as the methods usually employed for their determination.

Considerando com as exigências de economia de energia e redução de emissões de carbono, o nexo água vs. energia vem alcançando destacado interesse em todo o mundo. O Brasil ocupa uma posição singular na matriz energética mundial. A maior parte das habitações brasileiras tem eletricidade; e a expansão da matriz energética que, a princípio, possui meios adequados para sustentar o crescimento econômico, pode experimentar transformações. A determinação do Brasil pelos combustíveis alternativos foi uma escolha natural, dado seu potencial hidrelétrico e a extensão de terras agriculturáveis. No setor de transportes, o Brasil desenvolveu sua matriz energética com importante contribuição do etanol e do biodiesel. Embora esses combustíveis sejam baixos emissores de carbono, não são alternativas acessíveis quando considerados o uso da terra, segurança alimentar e water footprint. Desta forma, considerando os recentes avanços na exploração de petróleo do Pré-Sal (9-15 milhões de barris) e as recentes descobertas de jazidas de gás de xisto (245 tcf), juntamente às questões sociais e ambientais desfavoráveis dos biocombustíveis, a matriz energética brasileira poderá voltar a ter como foco os combustíveis fósseis. Estes desafios deverão ser resolvidos nas próximas décadas, refletindo não só no Brasil, mas também em todo o mundo.

According to the demands of energy saving and carbon emission reduction, the water vs. energy nexus has become a major concern worldwide. Brazil occupies a singular position in the global energy system. A major portion of the Brazilian occupancies has electricity and the energy system expansion that, at first, possesses adequate means for supporting the economic growing may experience some turnovers. The Brazil determination through alternative fuels was a natural choice, given its large hydropower potential and land agricultural base. In the transportation sector Brazil has developed its energy matrix towards an important rate of ethanol and biodiesel. Although those fuels are low carbon emitter, they may probably not be an affordable alternative regarding land use, food security and water footprint. In this way, considering the recent advances in the exploration of oil from Pre-salt (9-15 million barrels) and the discovery of shale gas wells up to 245 tcf, together to unfavorable social and environmental issues associated to biofuels, the Brazilian energy matrix might turn back to the fossil fuels again. These represent challenges to the Brazilian policymakers and how they will be solved will reflect not only in Brazil but also to the world at large.

A atmosfera de regiões costeiras adjacentes a regiões urbanas podem ser afetadas pela emissão de diferentes poluentes atmosféricos, dentre eles, os íons majoritários. Nesse estudo foram estudadas a composição química e as fontes de carboxilatos e íons solúveis em água em partículas finas e grossas bem como as estimativas de fluxo de deposição seca em um sítio em uma região costeira tropical afetada por uma Região Metropolitana. As concentrações médias de carboxilatos totais foram 78 ng m–3 na fração fina e 81 ng m–3na fração grossa do material particulado (MP). Os valores correspondentes de concentração para os íons inorgânicos foram 2143 ng m–3 e 4880 ng m–3, respectivamente, para as frações fina e grossa. As principais fontes para as partículas finas foram: (i)formação fotoquímica de ácidos carboxílicos na fase vapor e posterior conversão gás-partícula sobre partículas de sal marinho, (ii) emissões de fontes antrópicas envolvendo processos de transporte de longas distâncias; e(iii) a interconversão de espécies voláteis entre fases atmosféricas. Por sua vez, as fontes predominantes para as partículas grossas foram:(i) espécies gasosas ab/adsorvidas em partículas pré-existentes, (ii)emissão primária de partículas grossas de fontes antrópicas, e (iii) spray marinho e/ou ressuspensão do solo. Finalmente, a deposição seca de partículas representa o fluxo de íons majoritários na interface ar-oceano.

The coastal atmosphere adjacent to large urban areas can be strongly affected by the emission of air pollutants, among them, major ions species. In this study, the chemical composition and sources of carboxylates and other water-soluble ions in fine and coarse aerosols as well as estimates of particle dry deposition fluxes were studied at a tropical coastal site affected by an urban environment. The mean concentrations of the total carboxylates were 78 ng m–3 in fine fraction and 81 ng m–3 in coarse fraction of particulate matter (PM). The corresponding values for the total inorganic ions were 2143 ng m–3 and 4880 ng m–3 respectively. Main sources for fine particles were:(i) photochemical formation of carboxylic acids in vapor phase and a posterior gas-to-particle conversion onto sea salt particles; (ii) emissions from anthropic sources with long range transportation processes; and (iii) the interchanging of volatile species among atmospheric phases. In turn, for coarse particles, the predominant sources were: (i)gas-phase species and ab/adsorbed onto pre-existing particles afterwards;(ii) primary emission of coarse particles from anthropogenic sources; and (iii) sea salt spray and/or soil resuspension. Finally, particle dry deposition was a very important mechanism representing air-to-sea fluxes of major species.