scholarly journals Study on Formation Kinetics and Mechanism of Barium-Calcium Phosphoaluminate Mineral

2022 ◽  
Author(s):  
Jungang Yuan ◽  
Hao Liu ◽  
Fengnian Wu ◽  
Yongbo Huang ◽  
Jinghua Yan ◽  
...  
Keyword(s):  
Activation Energy ◽  
Calcination Temperature ◽  
Conversion Rate ◽  
Reaction Rate ◽  
Kinetics And Mechanism ◽  
Holding Time ◽  
Experimental Results ◽  
Formation Kinetics

Abstract Barium-calcium phosphoaluminate ((C,B)8A6P) mineral was synthesized by introducing Ba2+ into the lattice of calcium phosphoaluminate (C8A6P) mineral and it owned the better hydration activity than C8A6P. In this study, the formation kinetics and mechanism of (C,B)8A6P mineral was firstly systematically explored. The experimental results indicated that calcination temperature had a significant effect on the formation of (C,B)8A6P mineral. The conversion rate of (C,B)8A6P mineral was less than 0.5 and reaction rate was less than 9.4 × 10-7 with the holding time of 8 h at 1500-1530 °C. Nevertheless, the conversion rate and reaction rate reached 0.8 and 9.4 × 10-7, respectively, with the holding time of only 2 h when the calcination temperature ranged from 1540 °C to 1560 °C. In addition, the Jander equation was feasible for the formation of (C,B)8A6P with activation energy of 1310 kJ ∙ mol-1 at 1500-1530 °C, while the Ginstling equation was feasible for use with activation energy of 324 kJ ∙ mol-1 when the calcination temperature ranged from 1540 to 1560 °C.

Kinetics of CO2 Absorption in MEA+DETA Blended Amine Solutions

2013 ◽  
Vol 864-867 ◽  
pp. 194-200
Author(s):  
Juan Wen ◽  
Chun Xiu Huo ◽  
Bin Zhang
Keyword(s):  
Activation Energy ◽  
Dynamic Model ◽  
Rate Constant ◽  
Absorption Rate ◽  
Reaction Rate ◽  
Reaction Rate Constant ◽  
Experimental Results ◽  
Kinetics Of ◽  
Amine Solutions

The kinetics of CO2absorption in unloaded aqueous MEA, MDEA, DETA single amine solutions and MEA+DETA blende amine solutions was studied with the amine concentrations of 3.0 kmol/m3and at temperatures ranging between 298K and 338K. A dynamic model of CO2absorption rate on the basis of the static absorption experimental results was established. The reaction rate constant of CO2absorption in blended amine solutions MEA+DETA is , and its activation energy is 32.89KJ/mol.

Kinetics and mechanism of redox reactions of U(III) ions with monochloroacetic and dichloroacetic acids

1979 ◽  
Vol 44 (2) ◽  
pp. 401-405 ◽  
Author(s):  
Ľubica Adamčíková ◽  
Ľudovít Treindl
Keyword(s):  
Redox Reactions ◽  
Reaction Rate ◽  
Activation Parameters ◽  
Outer Sphere ◽  
Alcohol Concentration ◽  
Kinetics And Mechanism ◽  
Solvent Structure ◽  
Influence Of Ph ◽  
Sphere Mechanism

The kinetics and mechanism of the redox reactions of U3+ ions with mono- and dichloroacetic acids were studied. The influence of pH was observed mainly in the second case and led to the determination of the rate constants and activation parameters corresponding to two parallel steps, namely oxidation of U3+ with CHCl2COO- ions and oxidation of U3+ with CHCl2.COOH molecules. The influence of binary mixtures of water with methanol, ethanol, isopropanol, or tert-butenol on the reaction rate was followed. Increasing alcohol concentration influences the rate constant not only through changing dielectric constant and solvation of the reactants but also through a change of the solvent structure which plays a role in reactions with an outer sphere mechanism of the electron transfer.

scholarly journals Thermochemical Heat Storage in a Lab-Scale Indirectly Operated CaO/Ca(OH)2 Reactor—Numerical Modeling and Model Validation through Inverse Parameter Estimation

2021 ◽  
Vol 11 (2) ◽  
pp. 682
Author(s):  
Gabriele Seitz ◽  
Farid Mohammadi ◽  
Holger Class
Keyword(s):  
Numerical Model ◽  
Gas Flow ◽  
Reaction Rate ◽  
Heat Storage ◽  
Bulk Material ◽  
Fixed Bed ◽  
Experimental Results ◽  
Fixed Bed Reactor ◽  
Thermochemical Heat Storage ◽  
Speed Up

Calcium oxide/Calcium hydroxide can be utilized as a reaction system for thermochemical heat storage. It features a high storage capacity, is cheap, and does not involve major environmental concerns. Operationally, different fixed-bed reactor concepts can be distinguished; direct reactor are characterized by gas flow through the reactive bulk material, while in indirect reactors, the heat-carrying gas flow is separated from the bulk material. This study puts a focus on the indirectly operated fixed-bed reactor setup. The fluxes of the reaction fluid and the heat-carrying flow are decoupled in order to overcome limitations due to heat conduction in the reactive bulk material. The fixed bed represents a porous medium where Darcy-type flow conditions can be assumed. Here, a numerical model for such a reactor concept is presented, which has been implemented in the software DuMux. An attempt to calibrate and validate it with experimental results from the literature is discussed in detail. This allows for the identification of a deficient insulation of the experimental setup. Accordingly, heat-loss mechanisms are included in the model. However, it can be shown that heat losses alone are not sufficient to explain the experimental results. It is evident that another effect plays a role here. Using Bayesian inference, this effect is identified as the reaction rate decreasing with progressing conversion of reactive material. The calibrated model reveals that more heat is lost over the reactor surface than transported in the heat transfer channel, which causes a considerable speed-up of the discharge reaction. An observed deceleration of the reaction rate at progressed conversion is attributed to the presence of agglomerates of the bulk material in the fixed bed. This retardation is represented phenomenologically by mofifying the reaction kinetics. After the calibration, the model is validated with a second set of experimental results. To speed up the calculations for the calibration, the numerical model is replaced by a surrogate model based on Polynomial Chaos Expansion and Principal Component Analysis.

Investigation on the Rheological Behavior of Polyamide6/Montmorillonite Nanocomposites by Reactive Extrusion

2011 ◽  
Vol 233-235 ◽  
pp. 1998-2001 ◽  
Author(s):  
Ming Zhao ◽  
Xiao Zhong Lu ◽  
Kai Gu ◽  
Xiao Min Sun ◽  
Chang Qing Ji
Keyword(s):  
Activation Energy ◽  
Shear Stress ◽  
Shear Rate ◽  
Rheological Behavior ◽  
Reactive Extrusion ◽  
Shear Thinning ◽  
Experimental Results ◽  
Montmorillonite Nanocomposites

The rheological behavior of PA6/montmorillonite(MMT) by reactive extrusion was investigated using cone-and-plate rheometer. The experimental results indicated that PA6/MMT exhibited shear-thinning behavior. The shear stress of both neat PA6 and PA6/MMT increased with the increase in the shear rate. The reduction of the viscous activation energy with the increase of shear stress reflected PA6/MMT can be processed over a wider temperature.

scholarly journals Photoreduction of Cr(VI) Ions in Aqueous Solutions by UV/ Photocatalytic Processes

2012 ◽  
Vol 2012 ◽  
pp. 1-7 ◽  
Author(s):  
Chih Ming Ma ◽  
Yung Shuen Shen ◽  
Po Hsiang Lin
Keyword(s):  
Aqueous Solutions ◽  
Reaction Rate ◽  
Removal Rate ◽  
Experimental Results ◽  
Order Kinetic ◽  
Solution Ph ◽  
Relationship Of ◽  
The Relationship ◽  
Photocatalytic Processes ◽  
Order Kinetic Equation

This study discussed the photoreduction of Cr(VI) ions in aqueous solutions by UV/TiO2photocatalytic processes under various operational factors. Experimental results showed that the removal rate of Cr(VI) increased with decreasing solution pH values and with increasing dosages of organic compounds, indicating that the recombination rate of electrons and h+can be retarded in the reaction systems by the addition of the scavenger, thus raising the reaction rate of Cr(VI). The relationship of the chemical reaction rate of Cr(VI), TiO2dosage, and changes of Cr(VI) concentration was expressed by the pseudo-first-order kinetic equation. Comparing the experimental results of two different doping metals in modified TiO2photoreduction systems, the removal rate of Cr(VI) by the Ag/TiO2process is larger, possibly because the electron transferring ability of Ag is superior to that of Cu. However, the photoreduction rates of Cr(VI) by modified UV/TiO2processes are worse than those by a nonmodified commercial UV/TiO2process.

scholarly journals Molecular orbital study of the oxidation of steroidal phenols into quinols and epoxyquinols

2000 ◽  
Vol 65 (7) ◽  
pp. 491-496 ◽  
Author(s):  
Zoran Markovic ◽  
Bogdan Solaja ◽  
Dragan Milic ◽  
Ivan Juranic ◽  
Miroslav Gasic
Keyword(s):  
Activation Energy ◽  
Molecular Orbital ◽  
Experimental Results ◽  
Full Agreement ◽  
Radical Oxidation ◽  
Molecular Orbital Study ◽  
Orbital Study ◽  
Oxidation Of Phenols

The MO study showed that the radical oxidation of phenols into quinols occurs readily. Further radical oxidation (in the m-CPBA/(BzO)2/hv system) of quinols occurs through appropriate biradical species with an activation energy of 79.5 kJ/mol yielding syn-epoxyquinols. The stereochemical outcome presented in this study is in full agreement with the experimental results.

scholarly journals The effect of additives metal on the D.C conductivity of epoxy resin

2011 ◽  
Vol 8 (1) ◽  
pp. 168-174
Author(s):  
Baghdad Science Journal
Keyword(s):  
Activation Energy ◽  
Electrical Conductivity ◽  
Epoxy Resin ◽  
Filler Content ◽  
Experimental Results ◽  
Filler Concentration ◽  
Effect Of Additives

The present studies are focused on the modification of the properties of epoxy resin with different additives namely aluminum, copper by preparing of composites systems with percentage (20%, 40% and 50%) of the above additives. The experimental results show that the D.C of conductivity on wt% filler content at ( 293-413 ) K electrical conductivity of all above composites increased with temperature for composites with filler contact and find the excellent electrical conductivity of copper and lie between (2.6*10-10 - 2.1*10-10)?.cm . The activation energy of the electrical conductivity is determined and found to decrease with increasing the filler concentration.

scholarly journals Kinetics and mechanism of cetyltrimethylammonium bromide catalyzed oxidation of diethylene glycol by chloramine-T in acidic medium

2003 ◽  
Vol 68 (7) ◽  
pp. 535-542 ◽  
Author(s):  
V.W. Bhagwat ◽  
J. Tiwari ◽  
A. Choube ◽  
B. Pare
Keyword(s):  
Diethylene Glycol ◽  
Acidic Medium ◽  
Cetyltrimethylammonium Bromide ◽  
Reaction Rate ◽  
Chloride Ions ◽  
Kinetics And Mechanism ◽  
Product Analysis ◽  
Rate Determining Step ◽  
Chloramine T ◽  
Catalyzed Oxidation

The kinetics and mechanism of the C16TABcatalyzed oxidation of diethylene glycol (2,2?-oxydiethanol) by chloramine-T in acidic medium has been studied. The reaction has a first-order dependence on chloramine-T. With excess concentrations of other reactants, the reaction rate follows fractional order kinetics with respect to [diethylene glycol]. The micellar effect due to cetyltrimethylammonium bromide, a cationic surfactant, has been studied. The reaction is catalyzed by chloride ions as well. The small salt effect and increase in the reaction rate with increasing dielectric constant suggest the involvement of neutral molecules in the rate determining step. Addition of p-toluenesulfonamide retards the reaction rate. On the basis of product analysis, a pertinent mechanism is proposed.

Phase Formation Kinetics in Sol-Gel Derived Strontium Bismith Tantalate

2001 ◽  
Vol 666 ◽  
Author(s):  
Yun-Mo Sung ◽  
Woo-Chul Kwack
Keyword(s):  
Activation Energy ◽  
Thermal Analysis ◽  
Phase Formation ◽  
Sol Gel ◽  
Avrami Exponent ◽  
Fluorite Phase ◽  
X Ray Diffraction ◽  
Aurivillius Phases ◽  
Formation Kinetics ◽  
Isothermal Kinetic

ABSTRACTPhase formation characteristics of Sr0.7Bi2.4Ta2O9 (SBT) powder, synthesized via sol-gel and pyrolysis process, was investigated by using thermal analysis. Each of the two exotherms, appearing in differential thermal analysis (DTA) scan curves, was identified as crystallization of fluorite phase and transformation of fluorite to aurivillius phase, respectively by using x-ray diffraction (XRD). By applying non-isothermal kinetic analyses to the DTA results, activation energy values for the formation of fluorite and aurivillius phases were determined as 192 and 375 kJ/mol, respectively and Avrami exponent values for each reaction were determined as 0.91 and 0.96, respectively. These activation energy and Avrami exponent values were discussed in detail to understand phase formation mechanism in SBT system.

Predictive Kinetics-based Model for Shock-activated Reaction Synthesis of Ti3SiC2

2005 ◽  
Vol 20 (6) ◽  
pp. 1476-1484
Author(s):  
Jennifer L. Jordan ◽  
John A. Pelesko ◽  
Naresh N. Thadhani
Keyword(s):  
Heat Treatment ◽  
Activation Energy ◽  
Steady State ◽  
Predictive Model ◽  
Heat Dissipation ◽  
Experimental Results ◽  
Reaction Synthesis ◽  
Synthesis Conditions ◽  
Type Reaction ◽  
Activated State

A kinetics model based on mass and heat transport has been developed for Ti3SiC2 formation via shock-activated reaction synthesis of powder precursors. The model allows prediction of heat treatment conditions under which an otherwise steady-state reaction is taken over by a “run-away” combustion-type reaction during post-shock reaction synthesis of Ti3SiC2. Shock compression of Ti, SiC, and graphite precursors generates a densely packed highly activated state of reactants, which lowers the activation energy and results in an increased rate of formation of Ti3SiC2 at a lower temperature and in shorter times. The predictive model correlated with experimental results of fraction reacted as a function of time at heat-treatment temperatures of 1400 and 1600 °C illustrates an increased rate of reaction due to lowering activation energy, which also results in the reaction at 1600 °C being taken over by a “run-away” combustion-type reaction, as the rate of heat release due to reaction exceeds the rate of heat dissipation through the compact. Correlation of the model with experimental results illustrates that the predictive model can be used to optimize reaction synthesis conditions in shock-densified compacts of Ti3SiC2-forming powder precursors, to better understand the processes leading to a steady-state reaction being taken over by the combustion mode.

Sign in / Sign up

Export Citation Format

Share Document