Recuperação de compostos de iodo de reagentes e soluções laboratoriais

This work presents simple routes to recover iodine compounds from oxidized laboratory chemicals and aqueous solutions (HI and KI) used in laboratory chemistry classes. These routes are based on the oxidation of iodide ions (I-) to iodine (I2) by an oxidant (H2O2) or reduction of oxidized iodine by red phosphorus or hydrazine. Both routes presented high yields. The oxidative route is of general use whereas the reductive one is appropriate for restoring original iodine reagents. Final wastes were generated in low amounts. This work is appropriate for teaching many laboratory techniques (e.g., distillation, titration and filtration) in the chemical laboratory.

Determinação de glicerol livre e total em amostras de biodiesel por método enzimático com detecção colorimétrica

A method based on enzymatic activities was developed using three enzymes (glycerokinase, glycerol-3-phosphate oxidase and peroxidase) and colorimetric detection for the determination of glycerol in biodiesel. The enzymatic conversion of glycerol produces H2O2 that is eliminated by the action of peroxidase, an oxygen acceptor and 4- aminoantipirine, producing water and a colored compound, which was analyzed. This method showed good linear correlation coefficient (r = 0.9937) in the concentration range of 4.95 x 10-5 to 3.96 x 10-4% (w/w) and had experimental limits of detection and quantitation of 7.10 x 10-6 and 2.10 x 10-5% (w/w), respectively.

Degradação de corantes têxteis e remediação de resíduos de tingimento por processos Fenton, foto-Fenton e eletro-Fenton

In this work the degradation of textile dyes were evaluated, using Fenton, photo-Fenton and electro-Fenton processes. Under optimized conditions Fenton and photo-Fenton processes showed high decolorization capacity of the model dyes. The electro-Fenton process was carried out in an undivided electrochemical reactor (1000 mL) equipped with a carbon-felt cathode (253 cm²) and a platinum gauze anode (6 cm²). Under optimal conditions (J: 1.6 mA cm-2, Na2SO4: 0.075 mol L-1, pH: 3) H2O2 concentration of about 60 mg L-1 was observed. The addition of Fe2+ (15 mg L-1) induces Fenton reactions that permit almost total decolorization of textile dyes.

Actividad catalítica de metales de transición en la descomposición de peróxido de hidrógeno

This paper compares the catalytic activities of some transition metal ions (Fe3+, Co2+, Cu2+, Ni2+, Zn2+) in the H2O2 decomposition in homogenous and heterogeneous processes, including solid mixed systems (Fe-Cu-Co/Al2O3, Fe-Cu/Al2O3, Fe-Co/Al2O3 and Co-Cu/Al2O3). The solids were characterised by X-ray diffraction to explore evolution of phases or possible changes. Different trends of the catalytic activity were observed: in homogeneous medium the most active species was Fe3+, whereas in heterogeneous one the higher activities were shown for Co/Al2O3 and Co-Cu/Al2O3. A strong cooperative effect for the Co-Cu/Al2O3 system was observed, which can be considered as a new catalyst of interest for this type of reactions.

New strategies for treatment and reuse of spent sulfidic caustic stream from petroleum industry

This work examines traditional and new routes for removal of H2S and other sulfur compounds from spent sufidic caustic (SSC). SH- (hydrogenosulfide) and S2- (sulfide) ions were quantitatively oxidized at 25 ºC using H2O2, NaOCl or a spent sulfochromic mixture. SH-/S2- ions were also removed via reaction with freshly prepared iron or manganese hydroxides, or after passing the SSC through strong basic anion exchange resins (OH- form). The treated caustic solution, as well as iron/manganese hydroxides, removed H2S from diesel samples at 25 ºC. SSC treatment via strong basic anion-exchange resins produced the treated caustic solution with the highest free alkalinity.

Biomimetic oxidation of carbamazepine with hydrogen peroxide catalyzed by a manganese porphyrin

This laboratory project is planned for an undergraduate chemistry laboratory in which students prepare a manganese porphyrin able to mimic the oxidative metabolism of carbamazepine, one of the most frequently prescribed drugs in the treatment of epilepsy. The in vitro oxidation of carbamazepine results in the formation of the corresponding 10,11-epoxide, the main in vivo metabolite. The reaction is catalyzed by manganese porphyrin in the presence of H2O2, an environmentally-friendly oxidant. Through this project students will develop their skills in organic synthesis, coordination chemistry, chromatographic techniques such as TLC and HPLC, UV-visible spectrophotometry, and NMR spectroscopy.

Zn-edta degradation by catechol-driven fenton reaction

Zn-EDTA degradabilty by catechol-driven Fenton reaction was studied. Response surface methodology central composite design was employed to maximize this complex degradation. Theoretical speciation calculations were in good agreement with the experimental results. Fenton and Fenton type treatments are typically thought to be applicable only in the highly acidic range, representing a major operational constraint. Interestingly, at optimized concentrations, this CAT-driven Fenton reaction at pH 5.5 achieved 100% Zn-EDTA degradation; 60% COD and 17% TOC removals, using tiny amounts of CAT (50 µM), Fe(III) (445 µM) and H2O2 (20 mM) with no evident ferric sludge.

Treated domestic sewage: kinetics of Escherichia coli and total coliform inactivation by oxidation with hydrogen peroxide

Hydrogen peroxide has been used for decades in developed countries as an oxidizing agent in the treatment of water, domestic sewage and industrial effluents. This study evaluated the influence of the concentration of H2O2 and pH on the inactivation of Escherichia coli cells and the disinfection of sewage treated. The results showed that the inactivation rate increased with pH and H2O2. The presence of other contaminants dissolved in the effluent is probably the cause of these differences, because E. coli inactivation in synthetic wastewater was found to be much faster than in the real treated domestic sewage.

Aumento del contenido de ácidos húmicos en un carbón de bajo rango a través de la oxidación con aire y con peróxido de hidrogeno o ácido nítrico

Low-rank coals are an important source of humic acids, which are important in retention processes of water and nutrients in plants. In this study coal samples of Montelibano, Colombia, were oxidized with air at different temperatures and subsequently with H2O2 and HNO3. The materials were characterized by FTIR, proximate and elemental analysis, and quantification of humic acids. The oxidation process led to an increased content of oxygenated groups and humic acids in the carbonaceous structure. The solid oxidized with air at 200 ºC for 12 h and re-oxidized with HNO3 for 12 h showed the highest percentage of humic acids (85.3%).

Ocorrência e degradação de quinolonas por processos oxidativos avançados

In this review, the presence of quinolones in the environment, their risks and the available processes for water decontamination were addressed. Their occurrence in surface waters and also in soil raises concerns about the risk of the development of resistant bacteria and other potential chronic effects. AOPs (UV/H2O2, Fenton, photo-Fenton, and UV/TiO2) and ozonation proved effective for degrading these emerging contaminants due to hydroxyl radical formation, surpassing the efficacy of conventional methods. In addition, the main degradation mechanisms of these drugs as well as data on residual biological activity were analyzed.

Espécies ativas de oxigênio na resposta de defesa de plantas a patógenos

A explosão oxidativa é uma resposta de defesa da planta após o reconhecimento do patógeno, conduzindo à reação de hipersensibilidade (HR). Esta resposta é devido à geração de espécies ativas de oxigênio (ROS ou EAO's), tais como H2O2, O2-, e OH- As espécies ativas de oxigênio possuem várias funções na resposta de defesa da planta. Peróxido de higrogênio (H2O2) pode ser diretamente tóxico ao patógeno e está envolvido com o fortalecimento da parede celular, uma vez que o H2O2 é necessário para a biossíntese de lignina. Peróxido de hidrogênioatua também como mensageiro secundário, sendo responsável pela ativação da hidrolase do ácido benzóico, enzima responsável pela conversão do ácido benzóico em ácido salicílico. A explosão oxidativa não está confinada somente à HR macroscópica, uma vez que explosões oxidativas secundárias poderão ocorrer nos tecidos distantes, causando micro-HR's e conduzindo à resistência sistêmica adquirida (SAR), a qual é mediada pelo ácido salicílico como um sinal. Portanto, a ocorrência de HR e SAR é dependente da cascata de sinalização derivada da explosão oxidativa, que por sua vez é um evento inicial na resposta da planta contra a invasão do patógeno.

Localização de peróxido de hidrogênio durante a resposta de defesa de tomateiro contra Stemphylium solani

Peróxido de hidrogênio foi localizado citoquimicamente em virtude de sua reação com cloreto de cério, evidenciando H2O2 produzido em tomateiros (Lycopersicon esculentum) resistente e suscetível a Stemphylium solani. Precipitados de peridróxido de cério foram constatados nas células do mesofilo, na parede em contato com as hifas do patógeno. Portanto, não tendo sido observada reação diferencial entre as cultivares quanto ao acúmulo de H2O2, e, sendo sua presença detectada num dos controles negativos, sugere-se que este composto possivelmente não participe diretamente da resistência manifestada pela c.v. 'Motelle' contra S. solani, no tocante ao fortalecimento da parede celular.

Does cotinine act upon reactive oxygen species and peroxidases?

Nicotine, an oxidizing agent, is certainly one of the most widely used alkaloids in the world. It is, together with its main metabolite, cotinine, responsible for tobacco-dependence. The use of tobacco is closely associated with lung disease, morphological leukocyte modification and generation of oxidant species. The aim of this study was to look for a possible relationship between cotinine, oxidant species generation and oxidative processes. After studying the action of cotinine in some chemical oxidation models and on the enzymatic kinetics of peroxidases (myeloperoxidase and horseradish peroxidase), we concluded that cotinine does not act directly upon H2O2, HOCl, taurine chloramines, horseradish peroxidase or myeloperoxidase.

Adsorption of hidrogen peroxide on the surface of silica - titania mixed oxide obtained by the sol-gel processing method

This work describes the sol-gel mixed oxide SiO2/TiO2 property, ST, as prepared, and submitted to heat treatment a 773 K, STC. SEM and EDS images show, within magnification used, a uniform distribution of the TiO2 particles in SiO2/TiO2 matrix. Both, ST and STC adsorb hydrogen peroxide on the surface and through EPR and UV-Vis diffuse reflectance spectra, it was possible to conclude that the species on the surface is the peroxide molecule attached to the Lewis acid site of titanium particle surface, alphaTi(H2O2)+. As the material is very porous, presumably the hydrogen peroxide molecule is confined in the matrix pores on the surface, a reason why the adsorbed species presents an exceptional long lived stability.

Estudo do comportamento eletroquímico da enzima peroxidase na presença de peróxido de hidrogênio e ácido 5-aminossalicílico

O comportamento eletroquímico da enzima peroxidase (HRP) foi estudado utilizando o peróxido de hidrogênio como substrato enzimático e o ácido 5-aminossalicílico (5-ASA) como mediador de elétrons sobre eletrodo de grafite. Diversos parâmetros foram otimizados, tais como, o potencial aplicado à técnica amperométrica fixado em -0,125V, a solução tampão fosfato-citrato 0,1 mol L-1 pH 5,0 como eletrólito suporte e a proporção entre o 5-ASA e H2O2 em 1:7, entre outros. Foi observada a catálise da reação de oxidação do peróxido de hidrogênio na presença da enzima HRP e do mediador 5-ASA. O produto dessa oxidação foi reduzido na superfície do eletrodo, evidenciando um significativo aumento na intensidade da corrente catódica.