Application of the Organic Waste-Based Sorbent for the Purification of Aqueous Solutions

The effective purification of large-capacity wastewater from heavy non-ferrous metals and organic pollutants using inexpensive sorption technology remains a crucial task. Analyzing the current objectives of sustainable development, biochar obtained from chicken manure has prospects as a source for sorption purification of industrial wastewater. To determine the characteristics of organic material and the composition of the initial and equilibrium phases, the following analysis methods were used: volumetric, complexometric, pH-metric, X-ray fluorescence, chromatographic, spectrophotometric, luminescence-photometric and X-ray diffraction. The thermal nitrogen desorption method was used for determining the specific surface area and pore sizes with the Quantachrome Nova 1000e automatic analyzer. The sorption properties of the reprocessing product of the fresh poultry manure were investigated in relation to organic and inorganic compounds: phenols, benzene, ketones, cations of lead, mercury, manganese and iron. Based on the results obtained, technical conditions were developed for the use of the reprocessed organic waste-based product as a sorption material for household, industrial and technological wastewater purification from organic and inorganic components.

Specific surface area, crystallite size and thermokinetic of oxide formation γ → α-Al2O3 nano powders at 570 – 1470 K

Powders where the γ≈α-Al2O3-nano phases are the priority precursors for catalysts for heterogeneous catalysis with the maximum content of surface 5-coordinated Al centers for Pt attachment. Hydrogenated nano powders (~8 nm) of γ-, γ '-, θ-, κ-Al2O3 soluble in hydrochloric acid were obtained from the processing of aluminum boride powders with an icosahedral structure. Samples, which underwent a step-by-step and single heating of 50-100K heat treatment for 2 hours at temperatures of 570-1470K, were received in quantity of 34. The specific surface area of SВET, m2g-1 was measured by the thermal nitrogen desorption express method of gas chromatography through the GC-1 device. X-ray (phase and coherent), fluorescence and phase chemical-analytical evaluation of the samples were performed. The thermokinetic characteristics of the processes are calculated using the exponential Arrhenius law. Dimensional characteristics of crystallites (10.4-48 nm); specific surface area of powders (213-8.6 m2g-1, SВET); thermokinetic parameters of α-Al2O3 crystallite growth process (V α-Al2O3 - 1.44 10-3 - 6.67 10-3 nm s-1; E α-Al2O3 = 38.7±2.1kJ mol-1; A0 = 0.16±0.0 s-1 along the temperature line 1220-1470K were determined and calculated. The process of dehydration of two OH-groups occurs in the region 570-720K Ea H2O ↑ = 30.5 ± 0.5 kJ mol-1 A0 = 1.33±0.3 s-1. The last group of OH at temperatures of 820 -1070К and a rate of 2.13 10-4 - 4.93 10-4 mol s-1 Ea H2O ↑ = 13.2 ± 0.8 kJ mol-1 A0 = 16.9 ± 0.9 s-1. The activation energy of the phase transition is Ea., γ → α-Al2O3 = 23.9 ± 1.0 kJ mol-1 A0 = 2.01 ± 0.72 s-1 (770-970K) and Ea., γ → α-Al2O3 = 83.5 ± 0.8 kJ mol-1 A0 =(2,05±0,95) 103 s-1 (1070-1170K). It agrees well with the known heat of conversion Eа, γ→α-Al2O3 = 85 kJ mol-1. The TK of γ≈α-Al2O3-nano phases is at 1170K.

Nitrided Silicon-Carbon Coatings Structure and Properties

The paper considers structural and physicomechanical properties of silicon-carbon coatings deposited from a gaseous medium in doping with nitrogen ions. The analysis of the coatings by X-ray photoelectron spectroscopy shows that nitriding of silicon-carbon coatings promotes the formation of silicon nitride and compounds such as CNx and SixOyNz. A 1.5–2-fold increase in the content of sp2 -hybridized carbon and silicon carbide atoms is found to prevent silicon oxidation. Thermal annealing of the resulting silicon-carbon coatings increases the content of the graphite phase and silicon oxide.It is shown that doping of the working gas with nitrogen (Ar57 % + N43 %) leads to the formation of a more finely dispersed structure as compared to that when using argon only. During thermal annealing in air, the decreased carbon concentration and increased oxygen concentration can be observed due to silicon and carbon oxidation followed by desorption of carbon and oxygen compounds. In addition, annealing leads to nitrogen desorption from the coating. Nitriding of silicon-carbon coatings increases the dispersion of their structure, and heat-resistant compounds CNх, Si3N4 improve heat resistance and thermal stability of coatings, and increase microhardness and friction coefficient in friction units.

Improving Porosity of Glycerol-plated Silica from Rice Husk Silica

Research on the increasing pore size of rice husk silica with the addition of glycerol as a template has been done. Sodium silicate obtained from rice husk can be extracted with sodium hydroxide. The resulting sodium silicate is then added to the glycerol and followed by precipitation using hydrochloric acid to obtain silica. The obtained results were calcined at 600°C. The resulting material analised by FT-IR, XRD and BET. The FT-IR data shows an asymmetric Si-O-Si absorption peak at wave number 1067 cm-1 and a symmetrical Si-O-Si peak absorption at 806.77 cm-1 wave number. Diffractogram XRD also shows a widening peak in the area of 22.820 that the silica is amorphous. The result of adsorption of nitrogen desorption of silica isotherm indicated Type IV isotherm adsorption which was characteristic of mesoporous material and obtained the size distribution of 9.2 nm and the pore volume was 0.002850 cc / g and the surface area of silica was 80.38 m2/g

Анализ структурной эволюции порошков оксида цинка, полученных методом механического высокоэнергетического размола

Zinc oxide powders made by mechanical high-energy grinding have been investigated using the methods of scanning electron microscopy, thermal nitrogen desorption, and Raman spectroscopy of infrared Fourier spectroscopy. Their structural evolution, including reduction of the average size of crystallites, increase in specific surface area, as well as changes in the number and ratio of adsorption centers, has been demonstrated. The data on the reconstruction of the surface of zinc oxide powders and multiple bond breaking in near-surface areas resulting from long-term dispersion have been presented.

Correlating Synthesis Parameters to Morphological Entities: Predictive Modeling of Biopolymer Aerogels

In the past decade, biopolymer aerogels have gained significant research attention due to their typical properties, such as low density and thermal insulation, which are reinforced with excellent biocompatibility, biodegradability, and ease of functionalization. Mechanical properties of these aerogels play an important role in several applications and should be evaluated based on synthesis parameters. To this end, preparation and characterization of polysaccharide-based aerogels, such as pectin, cellulose and k-carrageenan, is first discussed. An interrelationship between their synthesis parameters and morphological entities is established. Such aerogels are usually characterized by a cellular morphology, and under compression undergo large deformations. Therefore, a nonlinear constitutive model is proposed based on large deflections in microcell walls of the aerogel network. Different sizes of the microcells within the network are identified via nitrogen desorption isotherms. Damage is initiated upon pore collapse, which is shown to result from the failure of the microcell wall fibrils. Finally, the model predictions are validated against experimental data of pectin, cellulose, and k-carrageenan aerogels. Given the micromechanical nature of the model, a clear correlation—qualitative and quantitative—between synthesis parameters and the model parameters is also substantiated. The proposed model is shown to be useful in tailoring the mechanical properties of biopolymer aerogels subject to changes in synthesis parameters.

Ammonia decomposition over Ni catalysts supported on perovskite-type oxides for the on-site generation of hydrogen

Ni/SrZrO3 and Ni/BaZrO3 catalysts showed high activity for ammonia decomposition since these supports promoted the nitrogen desorption step.