Kinetics of mullitization from sol-gel synthesized precursors

The aim of this study is to shed more light on the formation of mullite and the kinetics of mullitization from sol-gel synthesized precursors. Tetraethylorthosilicate (TEOS) and aluminum nitrate nonahydrate (ANN) were used, as a source of silica and alumina, respectively, for the synthesis of homogenous mullite precursor powder. The mullitization process was characterized by thermogravimetry (TG), differential thermal analysis (DTA), thermodilatometric analysis (TDA), and x-ray powder diffraction (XRD) techniques. It was found that mullite started to crystalize at temperatures of 1050, 1200, and 1241 °C as determined by XRD, DTA, and TDA, respectively?. Mullite crystallization kinetics was thoroughly investigated under isothermal and non-isothermal conditions using DTA. The activation energy for mullite formation was calculated, for different crystallization fractions, following the Freidman, Kissinger, Boswell, and Ozawa methods. The average values were found to be 1282.92, 1324.30, 1336.93, and 1283.09 kJ/mol, respectively. The kinetic parameters and the crystallization mechanism were determined and the results were compared with those available in the literature. The Sestak Berggren SB(m,n) model was found to be the most suitable for the determination of mullite crystallization mechanism. The calculated average values of the Gibbs free energy (ΔG^#), enthalpy (ΔH^#), and entropy (ΔS^#) for mullite formation, at different heating rates, were 433.98 kJ/mol, 1294.20 kJ/mol, and 566.23 J/mol.K, respectively.     

Facile Preparation of Mn3O4 Hausmanite Nanoplates from a New Octahedral Manganese (III) Schiff Base Complex

A novel bidentate Schiff base ligand L (L = N-(4-amino-2-chloro-phenyl)-2-hydroxybenzaldehyde) and the subsequent octahedral manganese(III) Schiff base complex MnL ₃ have been synthesized and characterized by, FT-IR spectroscopy and elemental analyses (CHN). Additionally, Schiff base ligand has been characterized by ¹H NMR spectroscopy. Thermogravimetric analysis of the ligand and its metal complexes reveals their thermal stability and decomposition pattern. Thus, the MnL ₃ complex has been investigated as a novel precursor for the facile preparation of Mn₃O₄ nanoparticles via solid-state thermal decomposition under aerobic conditions, at a temperature of ca. 450 °C The resulting Mn₃O₄ nanocrystals were characterized by FT-IR spectroscopy, X-ray powder diffraction (XRPD), transmission electron microscopy (TEM) and scanning electron microscopy (SEM). The XRPD studies reveal the characteristic diffraction peaks indexed to the Mn₃O₄ hausmanite structure, while the absence of additional peaks tends to clearly indicate the high purity of the sample. In addition, the TEM/SEM investigations displayed the nanoplate shape of the rather monodisperse crystalline Mn₃O₄ nanoparticles, with an average diameter of ca. 10 nm. The statistical distribution of the nanoparticles size has to be provided with an histogram graphic.     

Uniform continuity and growth of real continuous functions

The purpose of this paper is to understand whether there exists any link between the uniform continuity of a real function defined on an unbounded interval and its growth at infinity. The primary objective is to present some results from teaching experience which help in the comprehension of this notion and yield some classroom techniques. It is well known that a uniformly continuous function has a monomial growth; it will be proved that there does not exist another growth of positive order. After introducing three kinds of growth, some results are recalled in connection with the behaviour near infinity of a uniformly continuous function. Using a series of counterexamples, it is shown that the uniform continuity of a function cannot be described by its asymptotic behaviour near infinity. Finally, some useful properties of the averaging convergence are reviewed, and how this is related to uniform continuity is investigated.     

Preparation of new copolymer (polystyrene/TMSPM grafted on DDA-fractionated algerian montmorillonite) hybrid organoclay by radical copolymerization: structural study,thermal stability and hydrophobicity area

Journal of Thermal Analysis and Calorimetry - Polystyrene/organo-Algerian montmorillonite hybrid material was prepared by radical copolymerization of styrene monomer in the presence of the double...     

Solvent Mixture Optimization in the Extraction of Bioactive Compounds and Antioxidant Activities from Garlic (Allium sativum L.)

Garlic is a health promoter that has important bioactive compounds. The bioactive extraction is an important step in the analysis of constituents present in plant preparations. The purpose of this study is to optimize the extraction with the best proportion of solvents to obtain total phenolic compounds (TPC) and thiosulfinates (TS) from dried garlic powder, and evaluate the antioxidant activities of the optimized extracts. A statistical mixture simplex axial design was used to evaluate the effect of solvents (water, ethanol, and acetone), as well as mixtures of these solvents, after two ultrasound extraction cycles of 15 min. Results showed that solvent mixtures with a high portion of water and pure water were efficient for TPC and TS recovery through this extraction procedure. According to the regression model computed, the most significant solvent mixtures to obtain high TPC and TS recovery from dried garlic powder are, respectively, the binary mixture with 75% water and 25% acetone and pure water. These optimized extracts presented oxygen radical absorbance capacity. Pure water was better for total antioxidant capacity, and the binary mixture of water–acetone (75:25) was better for DPPH scavenging activity. These optimized extracts can be used for industrial and research applications.     

On Quantum Mechanics on Noncommutative Quantum Phase Space

In this work, we develop a general framework in which Noncommutative Quantum Mechanics (NCQM), characterized by a space noncommutativity matrix parameter θ=ε_ij^k θ_k and a momentum noncommutativity matrix parameter β=ε_ij^k β_k, is shown to be equivalent to Quantum Mechanics (QM) on a suitable transformed Quantum Phase Space (QPS). Imposing some constraints on this particular transformation, we firstly find that the product of the two parameters θ and β possesses a lower bound in direct relation with Heisenberg incertitude relations, and secondly that the two parameters are equivalent but with opposite sign, up to a dimension factor depending on the physical system under study. This means that noncommutativity is represented by a unique parameter which may play the role of a fundamental constant characterizing the whole NCQPS. Within our framework, we treat some physical systems on NCQPS : free particle, harmonic oscillator, system of two-charged particles, Hydrogen atom. Among the obtained results, we discover a new phenomenon which consists of a free particle on NCQPS viewed as equivalent to a harmonic oscillator with Larmor frequency depending on β, representing the same particle in presence of a magnetic field $\vec{B}=q^{-1}\vec{\beta}$. For the other examples, additional correction terms depending on β appear in the expression of the energy spectrum. Finally, in the two-particle system case, we emphasize the fact that for two opposite charges noncommutativity is effectively feeled with opposite sign.     

Influence of octadecylammonium, <Emphasis Type="Italic">N</Emphasis>,<Emphasis Type="Italic">N</Emphasis>-dimethylhexadecylammonium,and 1-hexadecyltrimethylammonium chloride upon the fractionated montmorillonite

The thermal degradation of thermally cured vinyl ester resin systems is studied for different heating rates. The kinetic triplets, the activation energy, pre-exponential factor and the reaction model f(α) for the different reaction extent of conversions (α) are estimated using advanced isoconversional methods. Although the thermal degradation curves show the degradation occurs as a single stage, the kinetic parameters suggest the otherwise. The activation energy remains constant for α?=?0.3–0.575 but varies during the initial and final stages of conversion. Similarly, the pre-exponential factor shows considerable variation between the lower and higher reaction extent (α) values. This shows the complexity in the reaction. The probable reaction mechanism that the degradation follows has been explained. The complexity of the thermal degradation and the changes in reaction model f(α) over different reaction extent has been related. The appropriate working temperature for different thermal lifetime of the cured vinyl ester resin system for the failure of conversion α?=?0.2 has been predicted under the nitrogen atmosphere.     

Analysis of biogenic amines in the brain of the American cockroach (Periplaneta americana) by gas chromatography-negative ion chemical ionisation mass spectrometry

Biogenic amines in the brain of the American cockroach have been identified and quantified by an extraction-derivatisation procedure involving their reaction with ditrifluoromethylbenzoyl chloride (DTFMB) in the aqueous phase followed by extraction into an organic solvent, hydrolysis of phenolic esters and conversion of free hydroxyl groups to trimethylsilyl (TMS) ethers and subsequent analysis by gas chromatography-negative ion chemical ionisation mass spectrometry. The molecular ion of these DTFMB-TMS derivatives carried most of the ion current which made the method highly specific and gave a potential limit of detection below the picogram level. This method establishes unequivocally that the principal amines in cockroach brain are tyramine, p-octopamine, dopamine, 5-hydroxytryptamine and noradrenaline. In contrast to mammalian nervous tissue, the other positional isomers of octopamine, together with the isomeric synephrines, are absent.