RESUMO: Este estudo teve como objetivo avaliar os efeitos da adição de cultura probiótica (Bifidobacterium animalis subsp. Lactis Bb-12) e prebióticos (fructooligosacarídeo - FOS) a formulações de iogurte armazenadas a 4°C por 28 dias, utilizando um planejamento experimental (variáveis independentes: (0-3% de FOS e cultura probiótica starter 0-3%). Foram analisados pH, acidez, gordura, sinérese, proteína, ºBrix, açúcares, FOS e contagem de bactérias probióticas. As formulações de iogurte adicionado de probiótico e prebiótico apresentaram menor acidez, sinérese e glicose quando comparados ao iogurte controle e também em comparação com as formulações contendo probiótico e prebiótico sozinhas. A formulação com 3% de probiótico e prebiótico apresentou menor perda de concentração de FOS e, após 28 dias, apresentou 1,5g de FOS por 100g (0,3% de kestose, 0,7% de nystose , 0,5% de fructosil-nistose). Além disso, a adição de prebióticos exerceu um efeito protetor sobre as bactérias probióticas e aumentou a sua sobrevivência.

ABSTRACT: This study aimed to evaluate the effects of adding probiotic culture (Bifidobacterium animalis subsp. Lactis Bb-12) and prebiotics (fructooligosaccharide - FOS) to yoghurt formulations stored at 4°C for 28 days, using an experimental design (independent variables: (0-3% of FOS and probiotic starter cultures 0-3%). The pH, acidity, fat, syneresis, protein, ºBrix, sugars, FOS and probiotic bacteria count were analyzed. The probiotic- and prebiotic-added yoghurt formulations showed lower acidity, syneresis and glucose than the control yoghurt and compared to formulations containing probiotic and prebiotic separately. The 3% probiotic and prebiotic formulation showed a lower loss of concentration of FOS, and after 28 days presented 1.5g of FOS per 100g (0.3% kestose, 0.7% nystose, 0.5% fructosyl-nystose). Furthermore, the addition of prebiotics exerted a protective effect on probiotic bacteria, enhancing their survival.

ABSTRACT Anaerobic biodigestion is an appropriate alternative for the treatment of swine wastewater due to its biogas generation properties and the possibility of its application as a source of energy for heating or electricity. However, digestate can still contain high levels of turbidity, organic carbon and nutrients and must be correctly managed as a biofertilizer, or treated to avoid any impact on the environment. Considering this, electrocoagulation (EC) shows promise as a technology because of its ease of handling and high efficiency in effluent remediation. This study aimed to evaluate the performance of EC in a batch system in the treatment of swine wastewater digestate. The wastewater used in the treatment was sampled from a 10 m3 biodigestor effluent (digestate) located at Concórdia, Santa Catarina, Brazil. A batch-scale experiment was carried out to evaluate the following two variables: electrode distance (ED) and voltage applied (V). The removal efficiency levels (%) for the best operational condition (2 cm, 5 V) after 30 min were: 97 %, 98 %, 77 % and 10 % for color, turbidity, total organic carbon (TOC) and total nitrogen (TN), respectively. The EC batch system produced efficient results, underlining its promise as an alternative to be applied in the treatment of digestate.

The objective of this work was the immobilization of the enzyme Candida antarctica lipase B (CAL B) using the sol-gel method of immobilization and three different initiators of the polymerization reaction: one acid (HCl), one basic (NH4OH) and the other nucleophilic (HBr). Tetraethylorthosilicate was used as the silica precursor. The influence of the additive PEG 1500 on immobilization was assessed. The efficiency of the process was evaluated considering the esterification activity of the xerogels. The immobilization process provided enhanced thermal stability, storage and operational aspects relative to the free enzyme. Storage temperature proved one of the main variables to be considered in the process, with the xerogels stored under refrigeration showing better results in terms of residual activity (nearly 200 days with ≥ 90% residual activity of basic and nucleophilic xerogels) when compared with storage at ambient temperature (nearly 40 days). The results demonstrated the possibility of reuse of derivatives and a greater number of cycles (nine), considering a residual activity of 50%.

A adulteração do produto Ilex paraguariensis com outras espécies de Ilex é um dos principais problemas dos produtores de erva-mate. Neste trabalho, três espécies de Ilex foram avaliadas quanto à sua composição volátil por microextração em fase sólida acoplada à cromatografia gasosa e detector de espectro de massas (HS-SPME/GC-MS). As espécies adulterantes I. dumnosa e I. theizans Mart. ex Reissek apresentaram um perfil diferente de compostos orgânicos voláteis, quando comparadas com a I. paraguariensis. Os aldeídos metil-butanal, pentanal, hexanal, heptanal e nonanal foram detectados apenas nas espécies adulterantes. Esse resultado sugere que esses compostos químicos são marcadores potenciais para a identificação de adulteração e análise da qualidade dos produtos à base de Ilex paraguariensis.

The adulteration of the product Ilex paraguariensis with other Ilex species is a mAjor problem for maté tea producers. In this work, three species of Ilex were evaluated for their volatile composition by headspace solid phase microextraction coupled to gas chromatography and mass spectrum detector (HS-SPME/GC-MS). The adulterating species I. dumnosa and I. theizans Mart. ex Reissek presented a different profile of volatile organic compounds when compared to I. paraguariensis. Aldehydes methyl-butanal, pentanal, hexanal, heptanal and nonanal were detected only in the adulterating species. This result suggests that such compounds are potential chemical markers for identification of adulteration and quality analysis of products based on Ilex paraguariensis.

This work aimed to assess the photocatalytic degradation of a model odor compound (dimethyl disulfide, DMDS), found in liquid and gaseous wastes of plants for processing poultry byproducts. The effect of pH and temperature on adsorption and photocatalytic degradation was evaluated through factorial experimental designs. The results suggest the presence of an optimum region for adsorption, at 45.0 ºC and pH 4.0. In the photocatalytic runs an optimum for temperature and pH was also observed. At 45 ºC and pH 4.0 the removal of DMDS was 99% after 60 min of irradiation.

Durante as análises de Demanda Química de Oxigênio (DQO) é gerado um efluente líquido que se caracteriza pela presença de elevadas concentrações de metais pesados (Hg, Ag, Cr e Fe). Visando à remoção seletiva destes metais, possibilitando suas reutilizações, foram avaliados diferentes agentes precipitantes (Cl-, Br-, I- e S= para a Ag e o Hg e NaOH, NH4OH e NaHCO3 para o Cr e o Fe). Para a Ag e o Hg os melhores resultados em termos de remoção e recuperação seletiva foram obtidos quando do emprego seqüencial dos íons cloreto e sulfeto. Devido à presença de Hg(I), se fez necessário o emprego de NH4OH para separar seletivamente a Ag, presente na forma de AgCl, precipitada concomitantemente com Hg(I) como Hg2Cl2. Para o Cr e o Fe foram obtidas remoções que satisfazem à legislação (FEPAM) para ambos os elementos, somente quando do emprego do NaOH como agente precipitante.

In the analysis of Chemical Oxygen Demand (COD) a liquid residue rich in heavy metals (Hg, Ag, Cr, Fe) is obtained. This work aimed to remove, in a selective way, such metals from the residue using chemical precipitation, also creating a possibility to recover and reuse the heavy metals,. Different precipitants were evaluated (Cl-, Br-, I- and S= for Ag and Hg, and NaOH, NH4OH and NaHCO3 for Cr and Fe). The best results for selective recovery of Ag and Hg were obtained using chloride followed by sulphide. Due to the presence of Hg(I) it is necessary the use of NH4OH to separate Ag and Hg(I) that are both precipitated as AgCl and Hg2Cl2. Removal of Cr and Fe that attends the local limits set by the official control agency (FEPAM) was only obtained when NaOH was used as precipitating agent.

Neste trabalho, apresenta-se um novo material adsorvente, obtido a partir da pirólise de resíduos da erva-mate. O carvão resultante demonstrou elevada área superficial específica quando comparado com outros materiais pirolisados e elevada capacidade de remoção de contaminantes orgânicos de soluções aquosas. Os valores de área específica apresentados pelos materiais foram de 344, 191 e ~0,5 m² g-1, para o carvão Mate 1, Mate 2 e Mate 3, respectivamente. As isotermas de adsorção mostraram que os carvões apresentam potencial para utilização como adsorvente para compostos orgânicos, tais como: o corante têxtil vermelho reativo, o corante azul de metileno e para o herbicida atrazina, sendo que os máximos de adsorção utilizando o carvão Mate 1 foram de 16, 230 e 30 mg g-1, respectivamente.

In this work we present a new adsorbent material, obtained by maté waste pyrolisis. The resulting charcoal presented high specific area when compared with other pyrolized materials and also high capacity to remove organic contaminants from aqueous solution. The charcoal showed specific area of 344, 191 and ~0.3 m² g-1 for sample Mate 1, Mate 2 and Mate 3, respectively. According to the corresponding adsorption isotherm these materials present good adsorption capacity for reactive textile and methylene blue dyes and the herbicide atrazine. Adsorption maxima were respectively 16, 230 and 35 mg g-1 for such substances, when sample Mate 1 was used.

Methane, the main constituent of natural gas (> 85%), is employed in large scale as an energy source (thermoelectric power plants, automobiles, etc). However, significant quantities of this gas contribute to the greenhouse effect. The catalytic combustion of methane can minimize these emissions. Palladium is one of the metals that shows the highest activity, depending on the different active forms of the metal. In this article, we focus on the influence of particle size and pretreatment on the catalytic performance of palladium in the methane combustion reaction.

KBrO3 is registered by the FAO/OMS as a genotoxic and carcinogenic compound. In spite of this, KBrO3 is still employed by Brazilian bakeries. Nowadays ion exchange chromatography (IEC) is the most rapid and trustful method for BrO3- analysis. When at high concentrations, chloride ions can interfere in the BrO3- analysis, if the detection is performed by electrical conductivity. On the other hand, spectrophotometric detection, presented here is based on the absorption of BrO3- in the ultraviolet region (210 - 230 nm) where the absortion of chloride ions is very low, thus making possible the qualitative and quantitative analysis of BrO3- in flour improver samples.

The tanning process in the leather industry generates very high quantities of chromium-containing solid waste ("wet blue" leather). Environmental concerns and escalating landfill-costs are becoming increasingly serious problems for the leather industry and an alternative disposal is needed. In this work, we are presenting a novel application for this solid waste, which is the removal of organic contaminants from aqueous-solution. The adsorption isotherm of "wet blue" leather waste from the AUREA tanning company in Erechim-RS (Brazil) showed that this material presents high adsorption capacities of the reactive textile dyes.

Contaminant gases in the atmosphere constitute an important problem to be solved in the world. The NOx gases produced as a consequence of engine high temperatures are deleterious to environment and human health, as they promote acid rain and can act in the same way as freons in the destruction of the ozone layer in the stratosphere. In this review, three way and selective reduction catalysts for decomposition of these contaminant gases are described. Details about conditions and problems, such as catalyst poisoning, and the search for new catalysts are shown.