The Process of Acetonitrile Synthesis over γ-Al[2]O[3] Promoted by Phosphoric Acid Catalysts

The influence of principal parameters (reaction temperature, ratio of acetic acid and ammonia, composition of reactionary mixture and promotion of catalysts) on the selectivity and yield of the desired product was studied in the reaction of catalytic acetonitrile synthesis by ammonolysis of acetic acid. The processing of [gamma]-Al[2]O[3] by phosphoric acid increases amount of the centers, on which carries out reaction of acetamide dehydration. The kinetic model of a limiting stage of reaction - the acetamide dehydration to acetonitrile was suggested. In the process of ammonolysis of acetic acid it was demonstrated that the use of catalysts promoted by phosphoric acid and ratio NH[3]:CH[3]COOH=(3-4):1 at temperatures of a reactor 360-390°С leads to the increase of acetonitrile productivity to 0.7-0.8 g/cm{3}·h and allows to minimize formation of by-products

Influence of concentration modifier on the structure and functional properties of aluminum oxyhydroxide modified

Studying the properties of nanomaterials is an important task, but nanomaterials with desired properties is a promising direction. The aim of this work is to investigate the influence of the value of the concentration of the modifier (ions Mn{2+}) on the structural and functional properties of modified aluminum oxyhydroxide. In this paper, using methods such as the X-ray diffraction studies, differential thermal analysis, electron microscopy, chromatography. The paper found that increasing the concentration of the modifier result in significant changes in the morphology, the appearance of metallic aluminum, which is well seen on X-ray data samples. The influence of thermal effects on a modified aluminum oxyhydroxide argon. Set the phase transition temperatures in the synthesized samples. It is shown that with increasing sodeozhaniya manganese in the composition of the synthesized samples decreases the value of specific surface area. Study of the functional properties showed that the synthesized material has catalytic properties in the oxidation of methane. It is shown that the effective sample is a sample with a manganese content of 2.7 wt. %. By XRD results calcined in air samples modified aluminum oxyhydroxide was shown that only in the sample with a manganese content of 2.7 wt. % MnAl[2]O[4] phase is formed, which is catalytically active phase

Synergistic effect in Ag/Fe-MnO2 catalysts for ethanol oxidation

Here we report the synergistic effect of OMS-2 catalysts tested in ethanol oxidation, and the effects produced by both the addition of an Fe modifier in the catalyst preparation stage, and the introduction of Ag on its surface by the impregnation method. To analyze the action of each component, the Fe-modified, Ag-containing OMS-2 catalysts with different Mn/Fe ratios were prepared. Combined XPS and XRF elemental analysis confirms the states and distribution of the Ag- and Fe-containing species between the surface and bulk of the OMS-2 catalysts, which form highly dispersed Ag species on the surface of 0.05Fe–OMS-2, and are also incorporated into the OMS-2 crystalline lattice. The cooperative action of Ag and Fe modifiers improves both reoxidation ability (TPO results) and the amount of adsorbed oxygen species on the catalyst surface. The introduction of Ag to the OMS-2 and 0.05 Fe–OMS-2 surface allows a high level of activity (T80 = 150–155 °C) and selectivity (SAc80 = 93%) towards the acetaldehyde formation

Catalytic Synthesis of Acetonitrile by Ammonolysis of Acetic Acid

The influence of principal parameters (reagent ratio, reaction temperature, temperature gradients along a catalyst layer) on the yield of the desired product was studied in the reaction of acetonitrile synthesis from acetic acid over γ-alumina. Thus, the increase in ammonia:acetic acid ratio leads to the increase in acetonitrile selectivity and yield. In this work it has been demonstrated that initial temperatures of 360-380 °C are optimum to effectively carry out the process of acetonitrile synthesis. The increase in reaction temperature allows one to increase the yield of acetonitrile, but at elevated temperatures the catalyst carbidization and contamination of the desired product were observed. The additives to the reaction mixture of the substances that decrease the rate of compaction products (CP) formation and participate in the desired product formation are very effective for decreasing the catalyst carbidization. The effect of the composition of a reaction mixture on a catalyst lifetime is considered. The addition of ethyl acetate to acetic acid promotes a greater carbidization as compared to pure acetic acid. The application of a mixture of acetic acid with acetic anhydride at similar acetonitrile yield decreases the catalyst carbidization

Process of catalytic synthesis of acetonitrile from acetic acid and ammonia at ?-Al2O3

In the reaction of catalytic synthesis of acetonitrile from acetic acid and ammonia the influence of ratio of reagents, reactor temperature, addition of acetic acid, acetic anhydrite and acetamide into the reaction mixture of ethyl ether as well as catalyst promotion (?-Al2O3) by phosphoric acid on the parameters of the process. Optimal conditions of the reaction are determined and the scheme of commercial prototype process is suggested

The convenient preparation of stable aryl-coated zerovalent iron nanoparticles

A novel approach for the in situ synthesis of zerovalent aryl-coated iron nanoparticles (NPs) based on diazonium salt chemistry is proposed. Surface-modified zerovalent iron NPs (ZVI NPs) were prepared by simple chemical reduction of iron(III) chloride aqueous solution followed by in situ modification using water soluble arenediazonium tosylate. The resulting NPs, with average iron core diameter of 21 nm, were coated with a 10 nm thick organic layer to provide long-term protection in air for the highly reactive zerovalent iron core up to 180 °C. The surface-modified iron NPs possess a high grafting density of the aryl group on the NPs surface of 1.23 mmol/g. FTIR spectroscopy, XRD, HRTEM, TGA/DTA, and elemental analysis were performed in order to characterize the resulting material