LaNiO3 material was synthesized by modified proteic method, calcined at 900 °C/2 h in air atmosphere and was applied to remove environmental contaminants. LaNiO3 phase with a perovskite structure was formed in the calcined material, which has a surface area of 22 m2 g-1 and is formed by fine particles agglomerated, with pH of the zero charge point of 7.44. The removal of a model pollutant (Turquoise Blue dye) indicated that the better removal occurs in acidic pH and with adsorbent’s mass of 50 mg, showing average value around 90% of removal efficiency and 131 mg g-1 for adsorption capacity (q) value. The variable constants model was the one that best fit the kinetic. LaNiO3 material resisted the test conditions and the recovery process, and maintained its high adsorption capacity throughout the six regeneration cycles studied, which indicates that it is a promising material as an adsorbent of pollutants and does not generate waste during the process.

Abstract Materials by the modified proteic method based on calcium doped LaMnO3 and LaNiO3, with perovskite structure were prepared. The X-ray diffraction patterns revealed the presence of the perovskite phase in all materials, whose specific surface area values varied between 27 and 37 m2.g-1. The materials presented efficiency for the removal of Congo red dye and those with site B occupied by nickel presented better adsorptive efficiency. The incorporation of calcium on LaMnO3 or LaNiO3 materials caused an improvement in the performance of the materials for the dye removal from water. The materials maintained perovskite structure after the adsorption tests, allowing their reuse in new adsorption tests with high efficiency.

Resumo Perovskitas do tipo La1-xSrxNiO3 (x= 0,0, 0,3 ou 0,7) foram sintetizadas utilizando o método do gel proteico modificado e usando colágeno como precursor orgânico. Catalisadores do tipo La1-xSrxNiO3/Al2O3 foram obtidos utilizando-se o método da impregnação úmida. Os catalisadores sintetizados foram caracterizados por difratometria de raios X, área superficial e redução à temperatura programada. Os catalisadores foram avaliados na reação de oxidação parcial do metano, e os níveis de seletividade ao CO, CO2, H2 e H2O foram determinados. Dentre os catalisadores estudados, o catalisador LaNiO3/Al2O3 foi o que apresentou maior nível de conversão de metano (78%) e maior seletividade ao H2 (55%).

Abstract La1-xSrxNiO3 (x= 0.0, 0.3 or 0.7) perovskite-type oxides were synthesized using the modified proteic gel method and using collagen as an organic precursor. Catalysts of La1-xSrxNiO3/Al2O3 were obtained using the wet impregnation method. The synthesized catalysts were characterized by X-ray diffraction, surface area and temperature-programmed reduction. The catalysts were evaluated in the partial oxidation reaction of methane, and the levels of selectivity to CO, CO2, H2 and H2O were determined. Among the catalysts studied, the catalyst LaNiO3/Al2O3 had the highest methane conversion level (78%) and higher H2 selectivity (55%).

Este trabalho descreve um estudo sobre a síntese da perovsquita LaNiO3 via método do gel proteico, variando quantidade de colágeno e sobre a atividade catalítica de LaNiO3 e LaNiO3/Al2O3 na produção de gás de síntese (CO + H2). Os padrões de difração de raios X revelaram a formação da estrutura perovsquita em todas as amostras preparadas pelo método de síntese do gel protéico, variando a quantidade de colágeno e após calcinações a 700 ºC por 2 h. O catalisador LaNiO3/Al2O3 preparado pelo método de impregnação mostrou picos de difração nos difratogramas atribuídos a LaNiO3 e ao suporte (Al2O3). Este catalisador apresentou: área superficial específica de 46,1 m² g-1, dois picos de redução no perfil de redução à temperatura programada (RTP) e 46% de conversão do metano (através da oxidação parcial do metano utilizando oxigênio) depois de 18 h de reação.

This work describes a study on the synthesis of LaNiO3 perovskites via the modified proteic gel method, varying collagen content and on the catalytic activity of LaNiO3 and LaNiO3/Al2O3 in the syngas (CO + H2) production. X-ray diffraction patterns revealed the formation of perovskite structure in all samples prepared by proteic gel synthesis method, varying collagen content and after calcinations at 700 ºC for 2 h. LaNiO3/Al2O3 catalyst prepared by the impregnation method showed diffraction peaks due to the perovskite structure and to the support (Al2O3). This catalyst presented: specific surface of 46.1 m² g-1, two reduction peaks in the temperature programmed reduction (TPR) profile and 46% of methane conversion (by the partial oxidation of methane using oxygen) after 18 h of reaction.

Cis- e trans decalina foram submetidas à reação com catalisadores de craqueamento, para estudar a formação de aromáticos numa fração particular de produtos líquidos do processo de craqueamento catalítico fluido (FCC). Um reator batelada em leito fluidizado, CREC, foi usado a 673 e 723 K com tempos de contato entre 3 e 15 s. Cis-decalina foi muito mais reativa. Apesar de diferenças induzidas e medidas na acessibilidade dos catalisadores, seus perfis de atividade foram similares, sugerindo que restrições difusionais não prevalecem. Os produtos foram hidrocarbonetos C1-C12, enquanto o coque foi muito baixo. Reações de isomerização, craqueamento, transferência de hidrogênio, abertura/contração de anel e alquilação ocorreram, e produtos das várias reações foram observados em tempos de reação muito baixos. Naftênicos bicíclicos C10 e aromáticos alquil-substituídos C7-C11 ou nafteno-aromáticos foram os produtos mais importantes. Um mecanismo de reação com três rotas iniciais (isomerização, abertura de anel e reações de transferência de hidrogênio) foi proposto.

Cis- and trans-decalin were reacted over cracking catalysts to study the formation of aromatics in a particular fraction of the liquid products obtained in the fluid catalytic cracking process (FCC). A batch, fluidized bed CREC riser simulator reactor was used at 673 and 723 K and contact times varied from 3 to 15 s. Cis-decalin was much more reactive. Despite differences induced and measured in their accessibility indices, the catalysts led to similar activity profiles, suggesting that diffusion restrictions do not prevail. Products were C1-C12 hydrocarbons while coke was very low. Isomerization, cracking, hydrogen transfer, ring opening, ring contraction and alkylation reactions occurred and products from the various reactions were observed at very short reaction times. Bicyclic C10 naphthenics and alkyl-substituted C7-C11 aromatics or naphtheno-aromatics were the most important products. A reaction mechanism with three initial routes (isomerization, ring opening and direct hydrogen transfer reactions) was proposed.

Complexes with the composition Ln(NO3)3.2DTPO.4H2O (Ln = Nd and Er) were synthesized and characterized by infrared and visible absorption spectra (solid state and solution). The results of the absorption spectra in the solid state suggest that metal-ligand bonds are essentially electrostatic in all complexes. The absorption spectra of the nitrate salt solution presented smaller values of the oscillator strength when compared to the spectra of the complexes in the same solvent.