Thermodynamic descriptions of the ternary Fe-B-Si system and its binary sub-system, B-Si, are developed in the context of a new Fe-B-X (X = Cr, Ni, Mn, V, Si, Ti, C) database. The thermodynamic parameters of the other binary sub-systems, Fe-Si and Fe-B, are taken from earlier assessments. Experimental thermodynamic and phase equilibrium data available in the literature has been used for the optimization of the thermodynamic parameters of the Fe-B-Si and B-Si systems. The solution phases are described using substitutional solution model and the compounds (silicides and borides) are treated as stoichiometric phases. The calculated and experimental thermodynamic and phase equilibrium data were found to be in good agreement.
Thermodynamic optimizations of the ternary Fe-B-Ti system and its binary sub-system, B-Ti are presented. The thermodynamic descriptions of the other binaries, Fe-Ti and Fe-B, are taken from the earlier studies slightly modifying the Fe-Ti system assessment. The adjustable parameters of the Fe-B-Ti and B-Ti systems are optimized in this study using the experimental thermodynamic and the phase equilibrium data from the literature. The solution phases of the system are described using the substitutional solution model and the compounds (including borides) are treated as stoichiometric phases. The results show a good correlation between the calculated and measured thermodynamic and phase equilibrium data.
The application of aqueous two-phase systems (ATPS) is a cost-effective and simple method of protein separation (including enzymes) from complex systems. The first stage of designing the protein purification process in an ATPS involves the identification of the conditions for the formation of a given extraction system. For this purpose, the conditions for the formation of ATPSs in a thermoseparating EO50PO50 polymer/potassium phosphates system have been studied. Factors determining the ATPS formation comprised: separation temperature (4ºC or 20ºC), phosphate solution pH (6, 7.5 or 9) as well as the concentration of NaCl introduced into the systems (0.085 M, 0.475 M and 0.85 M). ATPS without NaCl were prepared as well. The conditions for the formation of the primary EO50PO50/potassium phosphate ATPS were determined with their phase diagrams. It was observed that with an increase of phosphate pH and NaCl concentration in the system, there was a decrease of the EO50PO50 and phosphate concentrations necessary to form a primary ATPS. After the primary two-phase separation, the top phase (rich in the EO50PO50 polymer) was partitioned from the bottom phase (rich in phosphates). Next, by means of polymer phase thermoseparation, a secondary two-phase system was formed. In the secondary EO50PO50/phosphate ATPS, the bottom phase was formed by the concentrated EO50PO50 polymer (30-80% concentration), while the top phase by a solution composed mainly of water, containing phosphate ions and remains of EO50PO50 polymer (3-7%).
A mathematical model of austenite - bainite transformation in austempered ductile cast iron has been presented. The model is based on a model developed by Bhadeshia [1, 2] for modelling the bainitic transformation in high-silicon steels with inhibited carbide precipitation. A computer program has been developed that calculates the incubation time, the transformation time at a preset temperature, the TTT diagram and carbon content in unreacted austenite as a function of temperature. Additionally, the program has been provided with a module calculating the free energy of austenite and ferrite as well as the maximum driving force of transformation. Model validation was based on the experimental research and literature data. Experimental studies included the determination of austenite grain size, plotting the TTT diagram and analysis of the effect of heat treatment parameters on the microstructure of ductile iron. The obtained results show a relatively good compatibility between the theoretical calculations and experimental studies. Using the developed program it was possible to examine the effect of austenite grain size on the rate of transformation.
Thermodynamic descriptions of the ternary Fe-B-V system and its binary sub-system B-V, are developed using experimental thermodynamic and phase equilibrium data from the literature. The thermodynamic parameters of the other binaries, Fe-V and Fe-B, are taken from earlier assessments slightly modifying the Fe-V description. The work is in the context of a new Fe-B-X (X = Cr, Ni, Mn, V, Si, Ti, C) database. The solution phases are described using substitutional solution model. The borides are treated as stoichiometric or semi-stoichiometric phases and described with two-sublattice models.