scholarly journals CALCULATION OF THE TEMPERATURES OF THE CHEMICAL REACTIONS OF THE IRON STEPPED RECOVERY FROM HEMATITE WITH CO GAS AND GASIFICATION OF SOLID CARBON ACCORDING EXISTING FORMULAS AND BY STANDARD VALUES OF ENTHALPY AND ENTROPY OF SUBSTANCES

2021 ◽  
Vol 2 (39) ◽  
pp. 16-26
Author(s):  
S. Panteikov
Keyword(s):  
Free Energy ◽  
Chemical Reactions ◽  
Low Temperatures ◽  
Thermodynamic Assessment ◽  
Solid Carbon ◽  
Iron Recovery ◽  
Literary Sources ◽  
Standard Values ◽  
Enthalpy And Entropy ◽  
Co Gas

The article presents the results of a thermodynamic assessment of the possibility of chemical reactions of the stepped recovery of iron from hematite with a recovering gas CO, as well as the Bell-Boudoir chemical reaction. It has been established that for each of the indicated chemical reactions there is a certain temperature (called by the author as "boundary temperature"), up to or above which CO gas cannot be a recovering agent for lower iron oxide from higher or the metallic iron itself from wustite, as well as gasification of solid carbon; while the recovery of Fe3O4 from Fe2O3 is theoretically possible at any temperatures above 0 ° C, the recovery of FeO from Fe3O4 and the gasification of solid carbon are theoretically possible above certain temperatures (i.e. at elevated and high temperatures), and the recovery of iron from FeO is below a certain temperature (i.e. at low temperatures). The numerical values of the boundary temperatures for the reactions of iron recovery and its lower oxides, as well as the reaction of gasification of solid carbon are given; graphical dependences of the Gibbs free energy of the indicated chemical reactions on temperature are made according to the equations available in metallurgical literary sources, and according to the expressions derived in the article by the author.

Metallographic Estimation of the Number of Forming Metallic Particles Obtained during Direct and Indirect Reduction of Metals from Complex Oxides

2019 ◽  
Vol 946 ◽  
pp. 523-527
Author(s):  
Arman S. Bilgenov ◽  
P.A. Gamov ◽  
V.E. Roshchin
Keyword(s):  
Metal Forming ◽  
Solid Phase ◽  
Quantitative Estimation ◽  
Direct Reduction ◽  
Reduction Process ◽  
Complex Oxide ◽  
Experimental Results ◽  
Solid Carbon ◽  
Indirect Reduction ◽  
Co Gas

The direct reduction of metals from a complex oxide with low iron content by solid carbon and indirect reduction by CO gas were studied in a vertical laboratory resistance furnace at 1300 °C for an hour reduction time. The experimental results were described from the point of view of the electrochemical nature of the metal reduction process, that involves the interaction of ions and electrons in the oxide lattice. The technique was developed by using the two different software programs for the quantitative estimation of the areas, average size and number of the metal forming in a complex oxide with extensive fields of vision. The obtained results of the quantitative characteristics of the metal forming during solid-phase carbo-thermal reduction were presented. The processes of reduction by solid carbon and CO gas based on the areas occupied by metal particles were quantitatively compared. The experimental results and the prospects for further experimental work were assessed and outlined.

Dielectric relaxation of some aliphatic ketones in dilute solutions

1976 ◽  
Vol 54 (7) ◽  
pp. 794-799 ◽  
Author(s):  
M. P. Madan
Keyword(s):  
Free Energy ◽  
Relaxation Time ◽  
Dielectric Relaxation ◽  
Relaxation Mechanism ◽  
Relaxation Data ◽  
Nonpolar Solvents ◽  
Aliphatic Ketones ◽  
Entropy Of Activation ◽  
Enthalpy And Entropy ◽  
Dielectric Relaxation Behavior

The dielectric relaxation behavior of 2-butanone, 2-pentanone, 2-heptanone, and 3-nonanone in dilute nonpolar solvents, n-heptane, cyclohexane, benzene, and carbon tetrachloride has been studied in the microwave region at a number of temperatures. The relaxation data have been used to estimate the free energy, enthalpy, and entropy of activation for the relaxation mechanism. The values of the relaxation time for those solutions for which there are available known data agree well with other determinations. The results have been discussed in terms of dipole reorientation by intramolecular and overall molecular rotation and compared, wherever possible, with other similar studies on aliphatic molecules.

Dolomite Decomposition to (Ca,Mg)O Solid Solutions: An X-Ray Diffraction Study.Part II.

1984 ◽  
Vol 39 (10) ◽  
pp. 981-985 ◽  
Author(s):  
G. Spinolo ◽  
U. Anselmi Tamburini
Keyword(s):  
Free Energy ◽  
Low Temperatures ◽  
Particle Sizes ◽  
Diffusional Process ◽  
X Ray Diffraction ◽  
High Iron Content ◽  
X Ray ◽  
Energy Of Mixing ◽  
Free Energy Of Mixing ◽  
Low Pressures

Abstract The full decomposition of dolomites with low and high iron content at low temperatures and low pressures is discussed with reference to the free energy of mixing of the ternary system Ca. Fe, Mg/O. The actual products of the primary step are a couple of rock salt structured oxides close to the spinodal compositions and with very small particle sizes. A subsequent diffusional process can produce large crystallites with equilibrium compositions, but it is effective only when either a low-iron dolomite is used as starting material or higher temperatures are employed.

scholarly journals Rationalisation of the activities of phenolic (vitamin E-type) antioxidants

2003 ◽  
Vol 17 (4) ◽  
pp. 753-762
Author(s):  
Christopher J. Rhodes ◽  
Thuy T. Tran ◽  
Philip Denton ◽  
Harry Morris
Keyword(s):  
Free Energy ◽  
Vitamin E ◽  
Gibbs Free Energy ◽  
State Theory ◽  
Linear Free Energy Relationship ◽  
Free Energies ◽  
Gibbs Free Energy Change ◽  
Linear Free Energy ◽  
Free Energy Of Activation ◽  
Enthalpy And Entropy

Using Transition-State Theory, experimental rate constants, determined over a range of temperatures, for reactions of vitamin E type antioxidants are analysed in terms of their enthalpies and entropies of activation. It is further shown that computational methods may be employed to calculate enthalpies and entropies, and hence Gibbs Free Energies, for the overall reactions. Within the Linear Free Energy Relationship (LFER) assumption, that the Gibbs Free Energy of activation is proportional to the overall Gibbs Free Energy change for the reaction, it is possible to rationalise, and even to predict, the relative contributions of enthalpy and entropy for reactions of interest, involving potential antioxidants.

Optics of hexagonal pyrrhotine (~Fe9S10)

1965 ◽  
Vol 35 (270) ◽  
pp. 335-346 ◽  
Author(s):  
Kurt von Gehlen ◽  
Horst Pillier
Keyword(s):  
Single Crystal ◽  
Low Temperatures ◽  
Dispersion Curves ◽  
Phase Relations ◽  
Optical Data ◽  
Standard Values ◽  
Two Phases

SummaryReflectivities of a series of oriented polished sections through a single crystal of pyrrhotine (Fe1−αS) from Trepča, Yugoslavia, were measured by means of a spectral photometer attached to a microscope. This pyrrhotine consists of two phases, namely intermediate pyrrhotine (∼ Fe9S10) and monoclinic pyrrhotine (∼ Fe7S8), which were probably formed by exsolution. The phase relations of pyrrhotine at low temperatures are discussed. Optical data are given for the intermediate pyrrhotine from 440 to 660 mµ. From the reflectivities measured in air and oil against a carborundum standard, values of n, k, and κ were calculated for ω and ε and represented in dispersion curves. Also, sections through the various ‘indicating surfaces’ at 546 mµ are shown. The accuracy of the values, which should be approximately the same for other pyrrhotine phases, is discussed.

Comparison Between RCCE and Shock Tube Ignition Delay Times at Low Temperatures

2015 ◽  
Vol 137 (6) ◽  
Author(s):  
Ghassan Nicolas ◽  
Hameed Metghalchi
Keyword(s):  
Free Energy ◽  
Shock Tube ◽  
Ignition Delay ◽  
Low Temperatures ◽  
Reduction Technique ◽  
Experimental Measurements ◽  
Ignition Delay Times ◽  
Delay Times ◽  
Constrained Equilibrium ◽  
Rate Controlled

The rate-controlled constrained-equilibrium (RCCE) method is a reduction technique based on local maximization of entropy or minimization of a relevant free energy at any time during the nonequilibrium evolution of the system subject to a set of kinetic constraints. In this paper, RCCE has been used to predict ignition delay times of low temperatures methane/air mixtures in shock tube. A new thermodynamic model along with RCCE kinetics has been developed to model thermodynamic states of the mixture in the shock tube. Results are in excellent agreement with experimental measurements.

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