Maximum decomposition temperature thermal destruction

Kaolinite is transformed into X-ray amorphous state when activated in air. According to authors [14,15], amorphization involves the destruction of bonds between tetrahedral and octahedral layers inside the package, till the decomposition into amorphous aluminium and silicon oxides. Other researchers [ 16,17] consider that amorphized kaolinite conserves the initial ordering of the positions of silicon atoms while disordering of the structure is due to the rupture of A1 - OH, Si - O - A1 bonds and the formation of molecular water. Endothermic effect of the dehydration of activated kaolinite is shifted to lower temperatures while intensive exo-effect with a maximum at 980°C still conserves. When mechanically activated kaolinite annealed at 1(X)0°C, only mullite (3Al20j-2Si0j) and X-ray amorphous SiOj are observed. In this case, the phase with spinel structure which is formed under thermal treatment of non-activated kaolinite is not observed thus, mechanical activation leads to the formation of other phases. 

The mechanism of the process is that the polymer reactive centers promote the metal nucleation and aggregation, after which the thermolysis occurs and the metal-containing substance is redistributed. The maximum amount of copper being introduced in PS through a common solvent is about 10%. At the same time, the polymer presence increases the temperature of cadmium trihydrate-oxalate decomposition [97], and the decay products increase the initial temperature of PETF intensive destruction. The copper formate thermal decomposition in the highly dispersed PETF presence allows us to produce a metallopolymeric composition (20-34% of copper) where the NP size distribution is maximal at 4nm, without any chemical interaction between the components. 

Based on X-ray photoelectron spectroscopy (XPS), Fourier transform infrared (FTIR), electron spin resonance (ESR), Mbssbauer, and extended X-ray absorption fine structure spectroscopy (EXAFS) , van Veen and collaborators concluded that the thermal treatment at temperatures where catalytic activity is maximum ( 500-600°C) does not lead to complete destruction of the macrocycles, but rather to a ligand modification which preserves the Me-N4 moiety intact. Furthermore, the stability of this catalytic site is improved because the reactive parts of the ligands are bound to the carbon support and thus are no longer susceptible to an oxidative attack. Thermal treatments at higher temperatures (up to 850°C) led to some decomposition of the Me-N4 moiety, and thus to a decrease of the catalytic activity, and to the reduction of some of the ions to their metallic state. 

---