scholarly journals A Kinetic Study on the Preparation of AlNi Alloys by Aluminothermic Reduction of NiO Powders

Metals ◽  
2018 ◽  
Vol 8 (9) ◽  
pp. 675
Author(s):  
Cesar Beltran ◽  
Alfredo Valdes ◽  
Jesús Torres ◽  
Rocio Palacios
Keyword(s):  
Agitation Speed ◽  
Aluminothermic Reduction ◽  
Magnesium Concentration ◽  
Main Reaction ◽  
Powder Injection ◽  
Reaction Products ◽  
Mechanical Agitation ◽  
Melt Temperature ◽  
Kinetics Of ◽  
Parameters Of Interest

In this work, the experimental results obtained during the preparation of Al-Ni and Al-Ni-Mg alloys using the aluminothermic reduction of NiO by submerged powder injection, assisted with mechanical agitation are presented and discussed. The analyzed variables were melt temperature, agitation speed, and initial magnesium concentration in the molten alloy. For some of the experiments performed, it was found that the Ni concentration increased from 0 to about 3 wt-% after 90 min of treatment at constant temperature and constant agitation speed. In order to determine the values of the kinetic parameters of interest, such as the activation energy and the rate constants, the values of the results obtained were fitted to the kinetic formulae available. Moreover, the kinetics of the reaction were found to be governed by the diffusion of Al and Mg to the NiO boundary layer, where MgAl2O4 or Al2O3 were formed as the main reaction products. Finally, from a thermodynamic study of the system, the main reactions that took place are explained.

scholarly journals Copper (II) Mediated Oxidative Alkoxylation of White Phosphorus. Communication 1.

2010 ◽  
Vol 12 (3,4) ◽  
pp. 259
Author(s):  
R.R. Abdreimova ◽  
F.Kh. Faizova ◽  
A.A. Karimova
Keyword(s):  
Metal Ion ◽  
Phosphorous Acid ◽  
Inert Atmosphere ◽  
White Phosphorus ◽  
Main Reaction ◽  
Reaction Products ◽  
Dimethyl Phosphite ◽  
Trialkyl Phosphates ◽  
Oxidative Alkoxylation ◽  
Kinetics Of

White phosphorus has been oxidized by copper (II) acetylacetonate, halides or carboxylates in aliphatic alcohols to yield dialkyl phosphates and trialkyl phosphates under inert atmosphere and mild reaction conditions. Trialkyl phosphite has been observed as unstable organophosphorus intermediate, which is being converted into the main reaction products. In the case of methanolic solutions, the derivatives of two step acidolysis of dimethyl phosphite, monomethyl phosphite and phosphorous acid, have been additionally detected among the reaction products. The influence of the copper (II) oxidants on the kinetics of accumulation and transmutation of organophosphorus products has been explored. The order of oxidative ability of the copper (II) compounds has been established. The major steps of the reaction including (i) the coordination of white phosphorus and alcohol to metal ion and (ii) the redox decomposition of this intermediate complex accompanied by reducing elimination of elementary copper and formation of organophosphorus product have been also suggested.

scholarly journals Effect of Mg Concentration on the Aluminothermic Reduction of Mn2O3 Particles Obtained from Cathodes of Discharged Alkaline Batteries: Mathematical Modeling and Experimental Results

Metals ◽  
2019 ◽  
Vol 9 (1) ◽  
pp. 49
Author(s):  
Orlando Flores Dávila ◽  
Jesús Torres Torres ◽  
Alfredo Flores Valdes
Keyword(s):  
Molten Aluminum ◽  
Treatment Time ◽  
Chemical Reduction ◽  
Reduction Reaction ◽  
Solid Particles ◽  
Experimental Results ◽  
Aluminothermic Reduction ◽  
Magnesium Concentration ◽  
Reaction Products ◽  
Alkaline Batteries

This paper aimed at studying the effect of magnesium concentration in molten aluminum produced from beverage cans on the process of aluminothermic reduction of Mn2O3 particles obtained from the cathodes of discharged alkaline batteries. The experimental results were analyzed by using thermodynamic fundamentals and kinetic modeling, while the characterization of the reaction products obtained allowed the mechanism of the process to be described. It was found that the addition of magnesium improves the wettability of solid particles by molten aluminum, thus increasing the reaction and its subsequent incorporation into the molten aluminum solution of Mn released from the reduction reaction. This work was carried out using several initial magnesium concentrations; 1.0, 2.0, 3.0, and 4.0 wt %, under a constant temperature of 1073 K, a constant treatment time of 240 min, and a constant agitation speed of 200 rpm. The results show that the higher the initial magnesium concentration in the molten alloy, the higher the speed of the chemical reduction reaction of the Mn2O3 particles.

The Kinetics of Inhibition of the Action of Thrombin by the Fibrinopeptides Formed during the Clotting of Fibrinogen

1966 ◽  
Vol 16 (01/02) ◽  
pp. 277-295 ◽  
Author(s):  
A Silver ◽  
M Murray
Keyword(s):  
Amino Acids ◽  
Competitive Inhibition ◽  
Amorphous Material ◽  
Peptide Bond ◽  
Initial Reaction ◽  
Reaction Products ◽  
Coagulation Mechanism ◽  
Kinetics Of ◽  
Kinetics Of Inhibition ◽  
Burk Plot

SummaryVarious investigators have separated the coagulation products formed when fibrinogen is clotted with thrombin and identified fibrinopeptides A and B. Two other peaks are observed in the chromatogram of the products of coagulation, but these have mostly been dismissed by other workers. They have been identified by us as amino acids, smaller peptides and amorphous material (37). We have re-chromatographed these peaks and identified several amino acids. In a closed system of fibrinogen and thrombin, the only reaction products should be fibrin and peptide A and peptide B. This reasoning has come about because thrombin has been reported to be specific for the glycyl-arginyl peptide bond. It is suggested that thrombin also breaks other peptide linkages and the Peptide A and Peptide B are attacked by thrombin to yield proteolytic products. Thrombin is therefore probably not specific for the glycyl-arginyl bond but will react on other linkages as well.If the aforementioned is correct then the fibrinopeptides A and B would cause an inhibition with the coagulation mechanism itself. We have shown that an inhibition does occur. We suggest that there is an autoinhibition to the clotting mechanism that might be a control mechanism in the human body.The experiment was designed for coagulation to occur under controlled conditions of temperature and time. Purified reactants were used. We assembled an apparatus to record visually the speed of the initial reaction, the rate of the reaction, and the density of the final clot formed after a specific time.The figures we derived made available to us data whereby we could calculate and plot the information to show the mechanism and suggest that such an inhibition does exist and also further suggest that it might be competitive.In order to prove true competitive inhibition it is necessary to fulfill the criteria of the Lineweaver-Burk plot. This has been done. We have also satisfied other criteria of Dixon (29) and Bergman (31) that suggest true competitive inhibition.

Kinetics of the catalytic hydrodesulphurization reaction system; hydrogenolysis of thiophene

1980 ◽  
Vol 45 (10) ◽  
pp. 2728-2741 ◽  
Author(s):  
Pavel Fott ◽  
Petr Schneider
Keyword(s):  
Atmospheric Pressure ◽  
Active Sites ◽  
Flow Reactor ◽  
Kinetic Equations ◽  
Reaction System ◽  
Reaction Products ◽  
Molybdenum Catalyst ◽  
Cobalt Molybdenum Catalyst ◽  
Kinetics Of ◽  
Reaction Schemes

Kinetics have been studied of the reaction system taking place during the reaction of thiophene on the cobalt-molybdenum catalyst in a gradientless circulation flow reactor at 360 °C and atmospheric pressure. Butane has been found present in a small amount in the reaction products even at very low conversion. In view of this, consecutive and parallel-consecutive (triangular) reaction schemes have been proposed. In the former scheme the appearance of butane is accounted for by rate of desorption of butene being comparable with the rate of its hydrogenation. According to the latter scheme part of the butane originates from thiophene via a different route than through hydrogenation of butene. Analysis of the kinetic data has revealed that the reaction of thiophene should be considered to take place on other active sites than that of butene. Kinetic equations derived on this assumption for the consecutive and the triangular reaction schemes correlate experimental data with acceptable accuracy.

Kinetics of carbon monoxide methanation on a Ni/SiO2 catalyst

1990 ◽  
Vol 55 (7) ◽  
pp. 1678-1685
Author(s):  
Vladimír Stuchlý ◽  
Karel Klusáček
Keyword(s):  
Carbon Monoxide ◽  
Reaction Rate ◽  
Catalyst Activity ◽  
Adsorbed Hydrogen ◽  
Reaction Products ◽  
Co Methanation ◽  
Molar Ratios ◽  
Rate Determining Step ◽  
Higher Temperature ◽  
Kinetics Of

Kinetics of CO methanation on a commercial Ni/SiO2 catalyst was evaluated at atmospheric pressure, between 528 and 550 K and for hydrogen to carbon monoxide molar ratios ranging from 3 : 1 to 200 : 1. The effect of reaction products on the reaction rate was also examined. Below 550 K, only methane was selectively formed. Above this temperature, the formation of carbon dioxide was also observed. The experimental data could be described by two modified Langmuir-Hinshelwood kinetic models, based on hydrogenation of surface CO by molecularly or by dissociatively adsorbed hydrogen in the rate-determining step. Water reversibly lowered catalyst activity and its effect was more pronounced at higher temperature.

Study of kinetics of reaction of lignin model compounds with propylene oxide

Holzforschung ◽  
2008 ◽  
Vol 62 (2) ◽  
pp. 169-175 ◽  
Author(s):  
Krishna K. Pandey ◽  
Tapani Vuorinen
Keyword(s):  
Chemical Reaction ◽  
Propylene Oxide ◽  
Aqueous Media ◽  
Reaction Products ◽  
Model Compounds ◽  
Rapid Reduction ◽  
Visible Absorption ◽  
Lignin Model Compounds ◽  
Lignin Model ◽  
Kinetics Of

Abstract The etherification of phenolic groups has been found to inhibit photodegradation in wood and lignin rich pulps. The precise understanding of kinetics of chemical reaction between lignins or their model compounds and the etherifying agent is the first step for developing a viable modification procedure. In this study, we have investigated the reaction of lignin model compounds (namely, phenol and guaiacol) with propylene oxide in aqueous media. The kinetics of etherification reaction was studied under varying pH conditions in the temperature range 30–60°C. The etherified reaction products were characterized by gas chromatogram-mass spectrum (GC-MS). The extent of etherification of phenols and the rate of chemical reaction was followed by UV-Visible absorption spectroscopy. The reaction between lignin model compounds and propylene oxide was indicated by a rapid reduction in the absorbance accompanied by the development of a new band corresponding to etherified products. The reaction kinetics was investigated at pH ∼12 under the condition of excess concentration of propylene oxide. The reaction followed first order kinetics and rate constants increased linearly with an increase in the temperature and concentration of propylene oxide. The MS fragment data of reaction product support the proposed reaction scheme. The activation energy of the reaction of propylene oxide with phenol and guaiacol, calculated with the Arrhenius equation, was 56.2 kJ mol-1 and 45.4 kJ mol-1, respectively.

Kinetics of Low-Temperature Aluminothermic Reduction of Iron Tantalate

2021 ◽  
Vol 12 (5) ◽  
pp. 1400-1408
Author(s):  
R. I. Gulyaeva ◽  
A. M. Klyushnikov ◽  
S. A. Petrova ◽  
L. Yu. Udoeva
Keyword(s):  
Low Temperature ◽  
Aluminothermic Reduction ◽  
Reduction Of Iron ◽  
Kinetics Of

THE KINETICS OF THE OXIDATION OF GASEOUS ACETALDEHYDE

1932 ◽  
Vol 7 (2) ◽  
pp. 149-161 ◽  
Author(s):  
W. H. Hatcher ◽  
E. W. R. Steacie ◽  
Frances Howland
Keyword(s):  
Carbon Dioxide ◽  
Formic Acid ◽  
Induction Period ◽  
Reaction Vessel ◽  
Oxidation Products ◽  
Main Reaction ◽  
Chain Mechanism ◽  
Subsequent Reaction ◽  
A Chain ◽  
Kinetics Of

The kinetics of the oxidation of gaseous acetaldehyde have been investigated from 60° to 120 °C. by observing the rate of pressure decrease in a system at constant volume. A considerable induction period exists, during which the main products of the reaction are carbon dioxide, water, and formic acid. The main reaction in the subsequent stages involves the formation of peroxides and their oxidation products. The heat of activation of the reaction is 8700 calories per gram molecule. The indications are that the reactions occurring during the induction period are heterogeneous. The subsequent reaction occurs by a chain mechanism. The chains are initiated at the walls of the reaction vessel, and are also largely broken at the walls.

The kinetics of the photo-induced solid-state chemical reaction in Ag/As33S67bilayers and its reaction products

1999 ◽  
Vol 79 (2) ◽  
pp. 223-237 ◽  
Author(s):  
T. Wagner ◽  
E. Márquez ◽  
J. Fernández-Pena ◽  
J. M. González-Leal ◽  
P. J. S. Ewen ◽  
...  
Keyword(s):  
Solid State ◽  
Chemical Reaction ◽  
Reaction Products ◽  
State Chemical ◽  
Solid State Chemical Reaction ◽  
Kinetics Of
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