Combined Effects of Binary Chemical Reaction/Activation Energy on the Flow of Sisko Fluid over a Curved Surface

In this study, a modified Sisko fluid with Buongiorno model effects over a curved surface was considered. The MHD was applied normally to the flow direction, and the effects of chemical reacted and active energy at the curved surface is also discussed. We chose this pertinent non-Newtonian fluid model since it best represents blood composition, and thus helps us venture into complex blood flow problems. Since the flow is discharged over a curved shape, we therefore commissioned curvilinear coordinates to best portray our envisaged problem. We were also required to define various sundry parameters to make our mathematical equations easily solvable. Mathematical modelling was completed by considering traditional assumptions, including boundary layer approximation. Numerical simulation was conducted using MATLAB solver bvp4c. Several numerical tests were conducted to select the best blend of the linked parameters. We noticed thermal flux upsurged when the chemical reaction parameter was increased with the magnetic indicator parameter caused the flow to slow down, while an increasing amount of activation energy enhanced the concentration of the fluid. The numerical results and impacts of assorted parameters on different profiles are elaborated with the help of graphs and a table.

Research of the process of obtaining potassium fertilizers from carnallite ore

To providedomestic and foreign markets with potash fertilizers Kazakhstan has begun to create own production of these products. But at the moment enterprises engaged in mining potash salts did not reach a practical stage. The Chelkarcarnallite ore deposit is auniqueone in solving these urgent problems. The article presents results of the study of processing Chelkar potash ore washed from sodium chloride to obtain a potassium fertilizer containing potassium and magnesium sulfates. The kinetics of nitric acid decomposition of carnallite ore has been investigated. The calculated value of reaction activation energy of potassium sulfate and nitric acid inter-action characterizes the kinetic region of the process behavior.Optimal conditions for decomposition of washed calcined ore with 30%nitric acid solution at 50°C were determined. It has been found that to ensure better filtration properties and high rate of suspension separation, washed non-calcined ore should be used to exclude gypsum dehydration, which causes its phase conversion into anhydrite. The double salt of potassium-magne-sium sulfate was separated by crystallization from nitric acid extract and an ammoniated mother liquor drying allowed to obtain a salt, which is ballast-free chlorine-free complex nitrogen-potassium-magnesium fertilizer.

Cure kinetics and properties of high-performance epoxy thermosets cured with active ester-terminated poly (aryl ether ketone)

Benzene-1,3,5-triyl tribenzoate (TBB), both 3,5-bis(benzoyloxy)benzoate-terminated poly (aryl ether ketone) oligomers (BPAPK and TMPK), containing active ester (Ph−O−(C=O)− structure), were prepared and served as curing agents for dicyclopentadiene novoalc epoxy (DCPD). The curing kinetics and properties of three epoxy thermosets were systematically investigated. The model reaction of TBB and glycidyl phenyl ether was designed to understand the curing mechanism of oxirane ring with active ester. TMPK/DCPD displays the lowest reaction activation energy, which is the result of the combined influence of free volume and diffusion. In addition, TMPK/DCPD has the highest Tg value (218°C), which enhances 34.6% and 42.5% compared with BPAPK/DCPD and TBB/DCPD, respectively. Meanwhile, TMPK/DCPD also shows superior dielectric and water resistance properties due to no secondary alcohol generated after curing and hydrophobic tetramethyl-substituted biphenyl structure. Herein, TMPK/DCPD as high-performance epoxy thermosets has potential applications in electronic packaging fields.

Systematic Incorporation of Gold Nanoparticles onto Mesoporous Titanium Oxide Particles for Green Catalysts

This report describes the systematic incorporation of gold nanoparticles (AuNPs) onto mesoporous TiO2 (MPT) particles without strong attractive forces to efficiently serve as reactive and recyclable catalysts in the homocoupling of arylboronic acid in green reaction conditions. Unlike using nonporous TiO2 particles and conventional SiO2 particles as supporting materials, the employment of MPT particles significantly improves the loading efficiency of AuNPs. The incorporated AuNPs are less than 10 nm in diameter, regardless of the amount of applied gold ions, and their surfaces, free from any modifiers, act as highly reactive catalytic sites to notably improve the yields in the homocoupling reaction. The overall physical properties of the AuNPs integrated onto the MPT particles are thoroughly examined as functions of the gold content, and their catalytic functions, including the rate of reaction, activation energy, and recyclability, are also evaluated. While the rate of reaction slightly increases with the improved loading efficiency of AuNPs, the apparent activation energies do not clearly show any correlation with the size or distribution of the AuNPs under our reaction conditions. Understanding the formation of these types of composite particles and their catalytic functions could lead to the development of highly practical, quasi-homogeneous catalysts in environmentally friendly reaction conditions.

Molecular dynamics investigation of frictional decomposition behavior of HMX-tool interface in diamond cutting of HMX crystals

Purpose This paper aims to reveal the tribochemical reaction mechanism on the nano-cutting interface between HMX crystal and diamond tool. Design/methodology/approach Molecular dynamics simulation of HMX crystal nano-cutting by the reactive force field is carried out in this paper. The affinity of activated atoms and friction damage at the different interface have been well identified by comparing two cutting systems with diamond tool or indenter. The analyses of reaction kinetics, decomposition products and reaction pathways are performed to reveal the underlying atomistic origins of tribocatalytic reaction on the nano-cutting interface. Findings The HMX crystals only undergo damage and removal in the indenter cutting, while they appear to accelerate thermal decomposition in the diamond cutting. the C-O affinity is proved to be the intrinsic reason of the tribocatalytic reaction of the HMX-diamond cutting system. The reaction activation energy of the HMX crystals in the diamond cutting system is lower, resulting in a rapid increase in the decomposition degree. The free O atoms can induce the asymmetric ring-opening mode and change the decomposition pathways, which is the underlying atomistic origins of the thermal stability of the HMX-diamond cutting system. Originality/value This paper describes a method for analyzing the tribochemical behavior of HMX and diamond, which is beneficial to study the thermal stability in the nano-cutting of HMX.

The effect of calcium fluoride on extracting magnesium from magnesite and calcium carbonate by silicothermal reduction in flowing argon

At present, the production of magnesium is mainly carried out semi-continuously with ferrosilicon as reducing agent under high temperature and high vacuum. In order to continuously produce magnesium, anew method of extracting magnesium from low-grade magnesite and calcium carbonate by silicothermal method in flowing inert gas was proposed. The effects of calcium fluoride(CaF2)on decomposition rate, decomposition kinetics, reduction rate of magnesia and crystal type of dicalcium silicate in reduction slag were investigated in the paper. The experimental results showed that calcium fluoride could accelerate the decomposition of carbonate, and had no side effect on the calcined products. In addition, the analysis results of DTA curves showed that calcium fluoridecould reduce the decomposition reaction activation energy and the reaction temperature of carbonatein the prefabricated pellets. The results of reduction experiments showed that proper calcium fluoridecould promote the reduction rate of magnesia, and in the temperature range of 1250? ~ 1350?, with same timeframe, the corresponding calcium fluoride contents were5%, 3% and 1% respectively when the reduction rate reached the maximum. Excessive calcium fluoride could reduce the reduction rate of magnesia, but it couldpromote the transformation of dicalcium silicate to ? phase in the reduction slag.

Study on reaction kinetics of single slime

The study of the combustion characteristics of single slime fuels is the basis for achieving clean combustion of solid fuels. This paper uses a combination of experimental and theoretical analysis, combined with the Coats-Redfen integration method, to study the influence of ash content and heating rate on the kinetic parameters of coal slime, and solve the combustion kinetic parameters. The results show that under the same heating rate, the activation energy gradually increases. As the ash content of coal slime increases, the activity of the coal slime sample decreases, and the reaction activation energy gradually increases.

Study on detoxification property of alkaline-modified MoO42--H2O2 decontaminants against PhSMe under subzero environment

The decontaminant activated by MoO42- (MoO42--H2O2) suitable for subzero environment shows strong oxidizing ability and weak nucleophilicity due to its acid. In this paper, in order to improve nucleophilicity and retain oxidation of MoO42--H2O2 as far as possible, NH3 and NaOH were used as alkaline modifiers, and PhSMe was used as a simulant of HD to study the oxidation rate and products of sulfides by alkaline-modified MoO42--H2O2 below zero. Results showed that the reaction rate constants decreased with the increase of pH in both NH3 and NaOH modified MoO42--H2O2 at -20°C, and the relative ratio of sulfone to sulfoxide increased especially at pH>9. The reaction activation energy Ea of PhSMe oxidation in the alkaline-modified MoO42--H2O2 decontaminants was lower than that in the MoO42--H2O2 decontaminant, which indicated that the sensitivity of the oxidation reaction rate to temperature in MoO42--H2O2 was reduced after modification.

Recovery of Iron from Copper Slag Using Coal-Based Direct Reduction: Reduction Characteristics and Kinetics

The Fe3O4 and Fe2SiO4 in copper slag were successfully reduced to metallic iron by coal-based direct reduction. Under the best reduction conditions of 1300 °C reduction temperature, 30 min reduction time, 35 wt.% coal dosage, and 20 wt.% CaO dosage (0.75 binary basicity), the Fe grade of obtained iron concentration achieved 91.55%, and the Fe recovery was 98.13%. The kinetic studies on reduction indicated that the reduction of copper slag was controlled by the interfacial reaction and carbon gasification at 1050 °C. When at a higher reduction temperature, the copper slag reduction was controlled by the diffusion of the gas. The integral kinetics model research illustrated that the reaction activation energy increased as the reduction of copper slag proceeded. The early reduction of Fe3O4 needed a low reaction activation energy. The subsequent reduction of Fe2SiO4 needed higher reaction activation energy compared with that of Fe3O4 reduction.

Hydrodechlorination of carbon tetrachloride with nanoscale nickeled zero-valent iron @ reduced graphene oxide: kinetics, pathway, and mechanisms

In recent years, carbon tetrachloride (CT) has been frequently detected in surface water and groundwater around the world; it is necessary to find an effective way to treat wastewater contaminated with it. In this study, Ni/Fe bimetallic nanoparticles were immobilized on reduced graphene oxide (NF@rGO), and used to dechlorinate CT in aqueous solution. Scanning electron microscopy (SEM) demonstrated that the two-dimensional structure of rGO could disperse nanoparticles commendably. The results of batch experiments showed that the 4N4F@rGO (Fe/GO = 4 wt./wt., and Ni/Fe = 4 wt.%) could reach a higher reduction capacity (143.2 mgCT/gcatalyst) compared with Ni/Fe bimetallic nanoparticles (91.7 mgCT/gcatalyst) and Fe0 nanoparticles (49.8 mgCT/gcatalyst) respectively. That benefited from the nickel metal as a co-catalyst, which could reduce the reaction activation energy of 6.59 kJ/mol, and rGO as an electrical conductivity supporting material could further reduce the reaction activation energy of 4.73 kJ/mol as presented in the conceptual model. More complete dechlorination products were generated with the use of 4N4F@rGO. Based on the above results, the reductive pathway of CT and the catalytic reaction mechanism have been discussed.