Degradação de corantes ácidos por processos oxidativos avançados usando um reator com disco rotatório de baixa velocidade

Three technologies were tested (TiO2/UV, H2O2/UV, and TiO2/H2O2/UV) for the degradation and color removal of a 25 mg L-1 mixture of three acid dyes: Blue 9, Red 18, and Yellow 23. A low speed rotating disc reactor (20 rpm) and a H2O2 concentration of 2.5 mmol L-1 were used. The dyes did not significantly undergo photolysis, although they were all degraded by the studied advanced oxidation processes. With the TiO2/H2O2/UV process, a strong synergism was observed (color removal reached 100%). Pseudo first order kinetic constants were estimated for all processes, as well as the respective apparent photonic efficiencies.

Estudo da degradação de ranitidina via H2O2 eletrogerado/Fenton em um reator eletroquímico com eletrodos de difusão gasosa

The study of the electrochemical degradation of the ranitidine was developed using an electrochemical reactor with a gas diffusion electrode (GDE) as cathode. The electrolysis experiments was performed at constant current (1 < A < 10) and flow rate of 200 L h-1. The process of drug degradation, chemical/electrochemical and electro-Fenton ways, using electrochemical reactor showed best efficiency at current values of > 4 A. The process reached a production of 630 mg L-1 of the H2O2 at 7 A. The ranitidine concentrations was reduced in 99.9% (HPLC) and chemical oxygen demand (COD) was reduced in 86.7% by electro-Fenton.

Avaliação da degradação do diclofenaco sódico utilizando H2O2/fenton em reator eletroquímico

This paper describes a degradation study of the anti-inflammatory sodium diclofenac in aqueous medium using an electro-chemical flow reactor with a gas diffusion electrode as cathode. Two degradation processes were compared: by H2O2 electro-generated and H2O2 electro-generated/Fe(II). Concentration of sodium diclofenac was determined during the experiments by HPLC. The changes in chemical oxigen demand (COD) were also evaluated. Under the specific reaction conditions, 350 mg L-1 of H2O2 was electro-generated and 99.2% of sodium diclofenac was degradated, with 27.4% COD reduction. At the same conditions, but using Fe(II), drug degradation was 99.4% and the COD reduction was 63.2%.

Caracterização de cinza obtida por combustão de casca de arroz em reator de leito fluidizado

The rice husk combustion in a bubbling and atmospheric fluidized bed reactor was investigated. This paper presents the rice husk ash characterization employing the techniques of X-ray diffraction (XRD), X-ray fluorescence (XRF), and scanning electron microscopy (SEM) among others. After combustion, a rice husk ash containing 93% amorphous silica and <3% unburned char was produced. Methods usually applied to fixed bed considering external sources of energy and high reaction times were employed. Thus, the potential of this type of reactors with respect to speed, continuity and self-sufficiency energy of the process was shown.

Degradação eletroquímica do cloranfenicol em reator de fluxo

This paper reports a study of electrochemical degradation of the chloramphenicol antibiotic in aqueous medium using a flow-by reactor with DSA® anode. The process efficiency was monitored by chloramphenicol concentration analysis with liquid chromatography (HPLC) during the experiments. Analysis of Total Organic Carbon (TOC) was performed to estimate the degradation degree and Ion Chromatography (IC) was performed to determinate inorganic ions formed during the eletrochemical degradation process. In electrochemical flow-by reactor, 52% of chloramphenicol was degraded, with 12% TOC reduction. IC analysis showed the production of chloride ions (25 mg L-1), nitrate ions (6 mg L-1) and nitrite ions (4.5 mg L-1).

Reator de UV-Ozônio com lâmpada a vapor de mercúrio a alta pressão modificada para tratamento superficial de óxidos transparentes condutivos utilizados em dispositivos poliméricos eletroluminescentes

An UV-Ozone reactor was developed with an ignition tube extracted into HID mercury lamp used to irradiation on zinc oxide (ZnO) and fluorinated tin oxide (FTO) films for PLEDs devices. Different exposures times were used. In contact angle measurements revealed better results for ZnO and FTO by 15 and 5 min, respectively. In Diffuse Reflectance Infra-red Fourier Transformed (DRIFT) spectroscopy allowed the observation of water, hydrocarbon and carbon dioxide adsorbed on the untreated TCO surfaces. After the UV-Ozone treatment the contaminants were significantly reduced or eliminated and the PLEDs devices decreased threshold voltages in comparison with respectively untreated TCOs.

Remoção de corante por uso de Aspergillus niger AN400 em reator em bateladas sequenciais

A sequential batch reactor (4 L) inoculated with Aspergillus niger was operated in order to remove congo red dye (10 mg L-1). The feeding of the reactor was done to each 7 days. The glucose was added in the concentration of 1 g.L-1 (Stage I) and 0.5 g L-1 (Stage II). The Stage III occurred without glucose addition. The Stage I was great to process, because the system reached the greater dye removal (95%) as well as the kinetic parameters ware the best - K M (0.7 g L-1) and k1 (0.025 h-1).

Um reator fotoquímico barato e eficiente para experimentos de química

In this work, we present an efficient and inexpensive device for undergraduate chemistry classes aimed at teaching and learning the photolytic synthesis concepts. A photochemical reactor was tested for the synthesis of the organometallic compound enneacarbonyldiiron from iron pentacarbonyl in acetic acid, and its formation evidenced by FTIR analysis. Although similar devices have been described in other studies, none of these offered the simplicity, low cost, class-compatible reaction times and good yields afforded by the procedure reported herein.

Aplicação da radiação ultravioleta como forma de contribuição para a química verde e construção de um reator fotoquímico alternativo e de baixo custo, para pré-tratamento de amostras

Ultraviolet radiation corresponds to a fraction of electromagnetic radiation, covering wavelengths between 1 and 400 nm. Methods based on UV irradiation have become popular because it is possible to treat samples simply by applying energy, avoiding procedures that require the use of toxic substances, thus contributing to the development of Green Chemistry. This study aimed to assess the main applications of UV radiation reported in the literature and thoroughly described the construction of an alternative and low-cost photochemical reactor to be used for the pretreatment of samples in the laboratory. The use of this new photochemical reactor in the clean-up of milk samples for spectrofluorimetric measurements was also reported.

Desenvolvimento de reator tipo "dip catalyst" para filmes poliméricos contendo nanopartículas de metais de transição

This article describes the development of a new catalytic reactor designed to operate with nanoparticle-embedded polymer thin films. Stabilization of metal nanoparticles in films that serve as catalysts in organic reactions is relatively new; therefore, the development of reactors to facilitate their use is necessary. We describe in detail the preparation of the GDCR reactor-type "dip catalyst" and its evaluation in the Suzuki - Miyaura cross-coupling reaction of phenylboronic acid and 4-bromoanisole catalyzed by palladium nanoparticle-embedded cellulose acetate thin film (CA/PD(0)). Compared with earlier prototypes, GDCR reactor showed excellent results when operating with CA/PD(0) thin films.

CONSTRUÇÃO DE UM REATOR DE PLASMA DESCARGA CORONA PARA ELIMINAÇÃO DE COMPOSTOS ORGÂNICOS VOLÁTEIS

The impacts derived from the emission of volatile organic compounds (VOC) into the atmosphere can have harmful consequences for human health and the environment. In this regard, the present paper proposes the construction of a low-cost cold plasma reactor for the treatment of these compounds. Tests with the prototype were performed to confirm the efficiency for BTEX (benzene, toluene and xylene) samples. Degradation efficiency was confirmed by the gas chromatography method.

Desempenho de processo anaeróbio em dois estágios (reator compartimentado seguido de reator UASB) para tratamento de águas residuárias de suinocultura

Avaliou-se o efeito das águas residuárias de suinocultura com concentrações de sólidos suspensos totais em torno de 6.000 mg L-1 (DQOtotal variando de 7.557 a 11.640 mg L-1) no desempenho de processo anaeróbio em dois estágios compostos por reator compartimentado (ABR) e reator de fluxo ascendente com manta de lodo (UASB), instalados em série, em escala-piloto (volumes de 530 e 120 L, respectivamente), submetidos a tempos de detenção hidráulica (TDH) de 56 a 18 h no primeiro reator e de 13 a 4 h no segundo reator. As eficiências médias de remoção de DQOtotal variaram de 71,1 a 87,5% no reator ABR e de 41,5 a 50,1% no reator UASB, resultando em valores médios de 86,8 a 94,9% para o sistema de tratamento anaeróbio em dois estágios com carga orgânica volumétrica (COV), na faixa de 5,05 a 10,12 kg DQOtotal (m³ d)-1, no reator ABR, e de 2,83 a 9,63 kg DQOtotal (m³ d)-1, no reator UASB. As eficiências de remoção de SST e SSV foram da ordem de 95,6%. O teor de metano no biogás manteve-se acima de 70% para os dois reatores. A produção volumétrica de metano máxima de 0,755 m³ CH4 (m³ d)-1 ocorreu no reator 1, com COV de 10,12 kg DQOtotal (m³ d)-1 e TDH de 18 h. Os valores médios de pH variaram na faixa de 7,2 a 8,0 para os efluentes dos reatores 1 e 2. Os ácidos voláteis totais mantiveram-se estáveis com concentrações abaixo de 200 mg L-1. Com variações abruptas e acentuadas de concentrações de SST e DQOtotal do afluente, os reatores mantiveram as eficiências de remoção de DQO e sólidos suspensos, em torno de 70%, e a qualidade do biogás, com 80% de CH4.

Remoção de matéria orgânica, de nutrientes e de coliformes no processo anaeróbio em dois estágios (reator compartimentado seguido de reator UASB) para o tratamento de águas residuárias de suinocultura

Neste trabalho, avaliou-se o efeito das águas residuárias de suinocultura, com concentrações médias de sólidos suspensos totais variando de 4.591 a 13.001 mg L-1, no desempenho de processo anaeróbio, em dois estágios, compostos por reator compartimentado (ABR) e reator de fluxo ascendente com manta de lodo (UASB), instalados em série, em escala- -piloto (volumes de 530 e 120 L, respectivamente), submetidos a tempos de detenção hidráulica (TDH) de 60; 36 e 24 h no primeiro reator, e de 13,6; 8,2 e 5,4 h no segundo reator. As eficiências médias de remoção de DQOtotal variaram de 69 a 84% no reator ABR e de 39 a 58% no reator UASB, resultando em valores médios de 87 a 94% para o sistema de tratamento anaeróbio em dois estágios, com carga orgânica volumétrica (COV) na faixa de 11,5 a 18,0 g DQOtotal (L d)-1 no reator ABR, e de 4,2 a 13,4 g DQOtotal (L d)-1 no reator UASB. A produção volumétrica máxima de metano de 0,227 m³ CH4 (m³ reator d)-1 ocorreu no reator UASB, com COV de 10,6 g DQOtotal (L d)-1 e TDH de 5,4 h. As maiores eficiências de remoção de coliformes totais e termotolerantes (99,7%), DQOdiss (94%), SST (96%), NTK (71%), P-total (61%) e outros nutrientes, no sistema de tratamento anaeróbio em dois estágios, foram obtidas com o TDH de 73,6 h e temperatura climatológica média de 24,6 °C, aplicando-se a menor COV (de 11,5 g DQOtotal (L d)-1 no reator ABR, e de 4,2 g DQOtotal (L d)-1 no reator UASB) com a maior concentração de SST do afluente (13.001 mg L-1).

Partida de um reator anaeróbio horizontal para tratamento de efluentes do processamento dos frutos do cafeeiro

O presente estudo teve o objetivo de avaliar a partida e a adaptação de um reator anaeróbio horizontal de leito fixo (RAHLF) no tratamento de águas residuárias do processamento primário dos frutos do cafeeiro (ARC). O reator foi construído com tubos de PVC de 0,2 m de diâmetro e 3,2 m de comprimento. O sistema foi preenchido com cubos de espuma de poliuretano para imobilização de biomassa ativa. O reator apresentou volume total de 0,1 m³ e volume útil equivalente a 0,04 m³. Em média, houve remoção de 49% da matéria orgânica, com o reator trabalhando sob carga orgânica volumétrica média de 2,66 kg m-3 d-1, medida como DQO. A suplementação de alcalinidade, somada à inoculação prévia de biomassa, proporcionou partida estável do RAHLF, confirmada pelo consumo de ácidos voláteis e adaptação da microbiota ao resíduo. O sistema apresentou resistência às variações de vazão e de carga orgânica observadas, e os teores de fenol e potássio monitorados não causaram inibição da atividade biológica no RAHLF. O maior controle sobre as variações de carga é fator importante na continuidade dos estudos.