Search Results

You are looking at 91 - 100 of 147 items for

  • Author or Editor: A. Souza x
  • Refine by Access: All Content x
Clear All Modify Search
Journal of Thermal Analysis and Calorimetry
Authors: M. R. S. Silva, S. C. Souza, I. M. G. Santos, M. R. Cassia-Santos, L. E. B. Soledade, A. G. Souza, S. J. G. Lima, and E. Longo
Restricted access
Journal of Thermal Analysis and Calorimetry
Authors: S. C. Souza, I. M. G. Santos, M. R. S. Silva, M. R. Cassia-Santos, L. E. B. Soledade, A. G. Souza, S. J. G. Lima, and E. Longo
Restricted access
Journal of Thermal Analysis and Calorimetry
Authors: Mary Alves, Soraia Souza, Márcia Silva, Elaine Paris, S. Lima, R. Gomes, E. Longo, A. de Souza, and Iêda Garcia dos Santos

Abstract  

SrSnO3 was synthesized by the polymeric precursor method with elimination of carbon in oxygen atmosphere at 250 °C for 24 h. The powder precursors were characterized by TG/DTA and high temperature X-ray diffraction (HTXRD). After calcination at 500, 600 and 700 °C for 2 h, samples were evaluated by X-ray diffraction (XRD), infrared spectroscopy (IR) and Rietveld refinement of the XRD patterns for samples calcined at 900, 1,000 and 1,100 °C. During thermal treatment of the powder precursor ester combustion was followed by carbonate decomposition and perovskite crystallization. No phase transition was observed as usually presented in literature for SrSnO3 that had only a rearrangement of SnO6 polyhedra.

Restricted access
Journal of Thermal Analysis and Calorimetry
Authors: J. Maul, A. S. Brito, A. L. M. de Oliveira, S. J. G. Lima, M. A. M. A. Maurera, D. Keyson, A. G. Souza, and I. M. G. Santos

Abstract

Copper monoxide (CuO) was successfully obtained by microwave-assisted hydrothermal method, using different conditions—in a solution without base, in a solution alkalinized with NaOH or with NH4OH. The powders were analyzed by thermal analysis (TG/DTA), X-ray diffraction (XRD), infrared spectroscopy, UV–Visible spectroscopy, and scanning electronic microscopy. XRD results showed that CuO was obtained with monoclinic structure and without secondary phases. Thermal analysis and infrared spectra indicated the presence of acetate groups on the powder surface. TG curves also showed a mass gain assigned to the Cu(I) oxidation indicating that a reduction possibly occurred during synthesis. The high and broad absorption band in the UV–Vis spectroscopy from 250 to 750 nm indicated the coexistence of Cu(II) and Cu(I), confirming the Cu(II) reduction, inside the CuO lattice. It was also possible to confirm the Cu(II) reduction by a displacement of the Me–O vibration bands observed in the IR spectra at around 500 cm−1.

Restricted access
Journal of Thermal Analysis and Calorimetry
Authors: M. A. F. de Souza, A. G. Souza, R. A. Candeia, D. M. A. Melo, L. E. B. Soledade, M. R. C. Santos, I. M. G. Santos, S. J. G. Lima, and E. Longo
Restricted access
Journal of Thermal Analysis and Calorimetry
Authors: R. A. Candeia, F. S. M. Sinfrônio, T. C. Bicudo, N. Queiroz, A. K. D. Barros Filho, L. E. B. Soledade, I. M. G. Santos, A. L. Souza, and A. G. Souza

Abstract

Biodiesel oxidation is a complex process widely influenced by the chemical composition of the biofuel and storage conditions. Several oxidation products can be formed from these processes, depending on type and amount of the unsaturated fatty acid esters. In this work, fatty acid methyl and ethyl esters were obtained by base-catalyzed transesterification of soybean oil and physicochemically characterized according to standards from ASTM, EN, and ABNT. The thermal and oxidative stabilities of biodiesel samples were investigated during the storage process by pressure differential scanning calorimetry (PDSC) and by viscosity measurements. Absolute viscosities of biodiesels after accelerated aging were also determined. The viscosity increased as the aging temperature and time were raised. The results showed that oxidation induction can occur during storage, decreasing the biodiesel stability. PDSC analysis showed that during storage under climate simulation the values of high-pressure oxidative induction times (HPOIT) were reduced for both FAEE and FAME.

Restricted access

Sunflower biodiesel

Use of P-DSC in the evaluation of antioxidant efficiency

Journal of Thermal Analysis and Calorimetry
Authors: M. L. A. Tavares, N. Queiroz, I. M. G. Santos, A. L. Souza, E. H. S. Cavalcanti, A. K. D. Barros, R. Rosenhaim, L. E. B. Soledade, and A. G. Souza

Abstract

The higher is the degree of unsaturation in ester chain of a biodiesel, the smaller is its oxidation stability. Sunflower biodiesel obtained by the ethyl route possesses a high amount of unsaturated fatty acids, mainly oleic acid (C18:1) and linoleic acid (C18:2), thus being more prone to the oxidation process. In Brazil, with the purpose of meeting the specifications of the Brazilian National Agency of Petroleum, Natural Gas and Biofuels (ANP), antioxidant additives, from synthetic and natural origins, have been added to the biofuel. Antioxidants are an alternative to prevent the oxidative deterioration of the fatty acid derivatives, as they are substances able to reduce the oxidation rate. In this study, the oxidative stability of sunflower biodiesel, obtained by the ethyl route and additivated with different concentrations of the antioxidants butylated hydroxytoluene (BHT) and t-butylhydroquinone (TBHQ), was evaluated by means of Pressure differential scanning calorimetry (P-DSC) and the Accelerated oxidative stability test (Rancimat, Method EN 14112). The results obtained by the two techniques showed the same oxidation tendency. Thus, P-DSC can be used as an alternative to determine the oxidative stability of biodiesel. The antioxidant TBHQ, added to biodiesel at the concentrations of 2000 and 2500 mg kg−1, raised the oxidation induction time to a value higher than 6 h, the limit established by the Resolution ANP number 7/2008, thus being the best alternative among the studied antioxidants.

Restricted access

Abstract  

The conventional treatments of effluents containing heavy metals produce significant quantities of byproducts with recalcitrant characteristics, making necessary looking after alternative techniques in order to avoid the production of new contaminated residues. Sorption process of chromium and zinc in vertical columns loaded with sewage sludge and organic solid waste has been studied in this work. The data from the TG curves of the two sorbents presented significant differences when they were submitted to the metal uptake, being noticed the displacement of the thermal events towards lower temperatures for both types of sorbents studied. As it was expected, for both sorbents, an increase in the mass of samples has been observed at the completion of the thermal tests upon metal uptake. Therefore, these facts demonstrate that during the biosorption process a physico-chemical interaction took place between sorbents and metals, as it was evidenced by the more than 100 K increase in the decomposition temperatures as well as the variation of the ΔH values of the samples.

Restricted access
Journal of Thermal Analysis and Calorimetry
Authors: J. Botelho, A. Souza, L. Nunes, A. Chagas, I. Garcia dos Santos, M. da Conceição, and P. Dunstan

Abstract  

The standard molar enthalpies of formation of crystalline dialkyldithiocarbamates chelates, [Pd(S2CNR2)2], with R=C2H5, n-C3H7, n-C4H9 and i-C4H9, were determined through reaction-solution calorimetry in acetone, at 298.15 K. From the standard molar enthalpies of formation of the gaseous chelates, the homolytic (172.43.8, 182.53.2,150.93.1 and 162.63.1 kJ mol−1) and heterolytic (745.03.8, 803.73.3,834.33.1 and 735.23.0 kJ mol−1) mean palladium-sulphur bond-dissociation enthalpies were calculated.

Restricted access
Journal of Thermal Analysis and Calorimetry
Authors: F. L. Macedo, R. A. Candeia, L. L. M. Sales, M. B. Dantas, A. G. Souza, and M. M. Conceição

Abstract

Searching for other alternative sources, which are not part of the food chain, and which are able to supply the biofuel market is a promising option. In this context, it has been searched to investigate the oiticica oil, approaching its availability to the biodiesel synthesis, as well as its thermal stability. Few works retreat parameters such as: the optimization of the biodiesel synthesis, its physical–chemical properties, and thermal parameters etc. The characterization results revealed that the oil showed very high kinematic viscosity, and acidity value around 13 mg KOH/g, requiring a pre-treatment. To reduce the acid in the oil, it has been done the esterification of oil, which was studied in different molar ratios oiticica oil/ethanol (1:9) and 2.0% catalyst, in order to get the best reduction the index of acidity. The lowest level of acidity of the oil obtained after the esterification was 4.4 mg KOH/g. The reaction rate for the synthesis of biodiesel, compared to the initial mass of oiticica oil ester was 85%. This income can be overcome by pursuing an even smaller reduction of acid value of biodiesel oiticica. The acid value of biodiesel was 1.8 mg KOH/g. The results have revealed that the oiticica oil and biodiesel are stable at 224 and 179 °C, respectively.

Restricted access