Thermal Decomposition Mechanism and Non Isothermal Kinetics of Complex of [La_2(P-MBA)_6(PHEN)_2]2H_2O

The complex of [La 2(P MBA) 6(PHEN) 2]2H 2O (P MBA: p methylbenzoate and PHEN: 1,10 phenanthroline) was prepared and characterized by elemental analysis and IR spectroscopy. The thermal behavior of [La 2(P MBA) 6(PHEN) 2]2H 2O in dynamic nitrogen atmosphere was investigated by TG DTG techniques. The results show that the thermal decomposition process of the [La 2(P MBA) 6(PHEN) 2]2H 2O occurs in five steps. The empirical kinetic model for the first step thermal decomposition obtained by Malek method is SB(m,n). The activation energy E and the pre exponential factor lnA for this step reaction are 76.4 kJ·mol -1 and 24.92, respectively.

Studies on Non-isothermal Kinetics of Thermal Decomposition of Strontium Chloride Hexahydrate

The thermal decomposition of the strontium chloride hexahydrate and its kinetics were studied under non isothermal condition in nitrogen by thermogravimetric and derivative thermogravimetric techniques. The intermediate and residue for each decomposition were identified from TG curve. The non isothermal kinetic data were analyzed by the Achar method and the Coats Redfern method. The possible reaction mechanisms were suggested by comparing the kinetic parameters. The kinetic equation for the first stage can be expressed as d α /d t = A exp(- E/RT)(1-α ), the second stage, d α /d t = A exp(- E/RT)3(1-α ) 2/3 , and the third stage, d α /d t = A exp(- E/RT)3/2(1-α ) 2/3 [1-(1- α ) 1/3 ] -1 . Mathematic expressions of the kinetic compensation effects of each stage of the thermal decomposition reaction were also obtained.

Thermal debinding dynamics of novel binder system

The thermal debinding dynamics of newly developed binders for cemented carbides extrusion molding was studied. It is shown that the thermal debinding processes can be divided into two stages: low temperature region, in which the low molecular mass components (LMMCs) are removed; and high temperature region, in which the polymer components are removed. The rate of thermal debinding is controlled by diffusion mechanism. The thermal debinding activation energies were solved out by differential method and integral method. The results show that the addition of other components acted as a catalyzer can effectively decrease the activation energy of thermal debinding processes.

Synthesis, Characterization, Thermal Decomposition Mechanism and Non-Isothermal Kinetics of the Pyruvic Acid-Salicylhydrazone and Its Complex of Praseodymium(III)

The pyruvic acid salicylhydrazone and its new complex of Pr(III) were synthesized. The formulae C 10 H 10 N 2O 4 (mark as H 3L) and [Pr 2(L) 2(H 2O) 2]·3H 2O (L=the triad form of the pyruvic acid salicylhydrazone [C 10 H 7N 2O 4] 3- ) were determined by elemental and EDTA volumetric analysis. Molar conductance, IR, UV, X ray and 1H NMR were carried out for the characterizations of the complex and the ligand. The thermal decompositions of the ligand and the complex with the kinetic study were carried out by non isothermal thermogravimetry. The Kissinger's method and Ozawa's method are used to calculate the activation energy value of the main step decomposition. The stages of the decompositions were identified by TG DTG DSC curve. The non isothermal kinetic data were analyzed by means of integral and differential methods. The possible reaction mechanism and the kinetic equation were investigated by comparing the kinetic parameters.

Study on the thermal decomposition kinetics of nano-sized calcium carbonate

This study of the thermal decomposition kinetics of various average diameter nano-particles of cal-cium carbonate by means of TG-DTA(thermogravimetry and differential thermal analysis) showed that the thermal decomposition kinetic mechanisms of the same crystal type of calcium carbonate samples do not vary with decreasing of their average diameters ; their pseudo-active energy Ea; and that the top-temperature of decom-position Tp decreases gently in the scope of micron-sized diameter, but decreases sharply when the average di-ameter decreases from micron region to nanometer region. The extraordinary properties of nano-particles were explored by comparing the varying regularity of the mechanisms and kinetic parameters of the solid-phase reac-tions as well as their structural characterization with the variation of average diameters of particles. These show that the aggregation, surface effect as well as internal aberrance and stress of the nano-particles are the main reason causing both Ea and Tp to decline sharply with the decrease of the average diameter of nano-particles.

Kinetics of Therm al Decom position of[Eu_2(p-M O B A)_6(phen)_2](H_2 O)_2 in Static Air Atmosphere

The thermal decomposition of [Eu 2( p MOBA) 6(phen) 2](H 2O) 2 ( p MOBA=C 8H 7O 3, methoxybenzoate; phen=C 12 H 8N 2, 1,10 phenanthroline) and its kinetics were studied under the non isothermal condition in air by TG and DTG methods. The intermediate and residue for each decomposition were identified from TG curve. The non isothermal kinetic data were analyzed by the Achar method and Coats Redfern method. The possible reaction mechanisms were suggested by comparing the kinetic parameters. The kinetic equation for the first stage can be expressed as d α /d t = A exp(- E/RT )[-ln(1- α )] -1 , the second stage and the third stage d α /d t = A exp(- E/RT )3/2(1- α ) 4/3 [1/(1- α ) 1/3 -1] -1 . The mathematical expressions of the kinetic compensation effects of each stage of the thermal decomposition reaction were also obtained.

Detect early stage lung cancer by a LAMP microfluidic chip system with a real-time fluorescent filter processor

This work presents a promising clinical molecular diagnostics for early stage lung cancer. This novel diagnostic method utilized the loopmediated isothermal amplification （LAMP）, micro fluidic chips and a confocal optical detector with a nonlinear fluorescent filter processor. An isothermal amplification based microfluidic chip for the early diagnostics of lung cancer was developed and a confocal optical detector was improved by a novel real-time fluorescent filter to sensitively monitor the DNA amplification procedure with high signal to noise ratio and fluorescence collecting ability. Experiment showed that a rapid diagnostic of lung cancer by detecting the existence of the CEA mRNA could be performed in only 5 laL of reaction assay in less than 45 min. While the traditional intube RTPCR set consumed more than 25 -μL of the assay and took more than 90 rain.