Thermodynamic modelling of roasting of molybdenum sulphide concentrate with calcium hydroxide

This work aims to determine the conditions for the CaMoO4, CaSO4, Ca(ReO4)2 formation during oxidation of MoS2 and ReS2 in the presence of Ca(ОН)2. The concentrate from the Yuzhno-Shameyskoye deposit in the Sverdlovsk region, having 37% wt. Мо and 0.005% wt. Re, was selected as a feedstock for thermodynamic modelling of sweet roasting in the presence of Ca(OH)2. To determine the optimal amount of calcium-containing additives, the thermodynamic modelling was carried out using the following mass ratios: molybdenum concentrate: Ca(OH)2 = 1:0.8, 1:1, 1:1.2 and 1:1.5 in the temperature range of 100–800°С, with a step of 100°С, system pressure of 0.1 MPa in the air (molar ratio: molybdenum concentrate + Ca(OH)2: air = 1:5). The content of all sample components in moles was entered into the HSC 6.1 software package. The main reactions associated with the sweet roasting of molybdenum concentrate in the presence of calcium hydroxide were shown. It was established that the main phases formed as a result of roasting comprise CaSO4, CaSO3, MoO3, CaMoO4, CaMoO3 and CaReO4. The effect of temperature on the formation of the main gaseous products was studied under different mass ratios of molybdenum concentrate and Ca(OH)2. It was found that up to 600°C, with molybdenum concentrate to Ca(OH)2 ratio of 1:1, the concentrations of released sulphurous anhydride are lower than the maximum permissible concentrations. The calculated thermodynamic data was used for modelling the roasting process of molybdenum concentrate with calcium hydroxide. An optimal ratio necessary for the successful process operation was established: molybdenum concentrate: Ca(OH)2 = 1:1 by weight. Thermodynamic modelling showed that, in the temperature range of 100–600°С when using Ca(OH)2, no rhenium and molybdenum loss is observed, the release of sulfur is less than 10 mg/m3.

Pyrolysis of RDF and Catalytic Decomposition of the Produced Tar in a Char Bed Secondary Reactor as an Efficient Source of Syngas

One of the technical limitations of refuse-derived fuel (RDF) pyrolysis is the high content of tar in its gas products. In order to resolve this problem, a two-stage RDF pyrolysis with a catalyst based on char from RDF pyrolysis is proposed. This paper presents the results of municipal waste pyrolysis beginning in an oven heated to 480 °C and ending with catalytic tar cracking carried out in the temperature range from 800 to 1000 °C. Thermal and catalytic pyrolysis with a char catalyst containing a minimum of 6% Fe resulted in increases in the CO and H2 contents in gas products and decreases in CO2 and CH4. At 1000 °C, the mass ratio of gaseous products to liquids was greater than 6. The residence time of the gases in the catalytic zone was about 3–5 s. The reactor was a good source of hydrogen and carbon monoxide.

Porous SiC and SiC/Cf Ceramic Microspheres Derived from Polyhydromethylsiloxane by Carbothermal Reduction

A simple and inexpensive method for the preparation of porous SiC microspheres is presented. Polysiloxane microspheres derived from polyhydromethylsiloxane (PHMS) cross-linked with divinylbenzene (DVB) were ceramized under conditions leading to the removal of oxygen from the material. The content of free carbon (Cf) in highly crystalline silicon carbide (SiC) particles can be controlled by using various proportions of DVB in the synthesis of the pre-ceramic material. The chemical structure of the ceramic microspheres was studied by elemental analysis for carbon and oxygen, 29Si MAS NMR, 13C MAS NMR, SEM/EDS, XRD and Raman spectroscopies, and their morphology by SEM, nitrogen adsorption and mercury intrusion porosimetries. The gaseous products of the thermal reduction processes formed during ceramization created a porous structure of the microspheres. In the SiC/Cf microspheres, meso/micro pores were formed, while in carbon-free SiC, microspheres macroporosity dominated.

Nonoxidizing heating of chip‑powder dispersions of ferrous metals in hydrocarbon atmosphere

The process of inorganic and organic components temperature transformation of metal waste into solid and gaseous products in a continuous hot briquetting muffle furnace has been studied. The composition of the hydrocarbon atmosphere formed in the muffle under conditions of limited access to the oxidizer has been determined. It is shown that the thermal destruction of the coolant oil phase proceeds according to a complex mechanism of consecutive reactions, including polycondensation, polymerization, and deep compaction with a constant decrease in the hydrogen content and ends with the formation of a coke‑like carbon residue on the surface of metal particles and an air suspension of finely dispersed carbon particles (smoke). When it is heated to hot briquetting temperatures of 750–850 °C, chemically active dispersions of ferrous metals are protected from oxidation first by a hydrocarbon gas with a density of 9.0–13.5 kg/m3, then by a pyrocarbon coating with a thickness of 0.1–0.3 mm up to the completion of the processes of pressing and cooling the briquette.

Thermal analysis of building materials for decoration and INFRARED spectroscopy of gaseous products of their thermal destruction

В настоящей статье представлены результаты экспериментального исследования термической деструкции отделочных строительных материалов и идентификации продуктов их термического разложения. Исследование термической деструкции отделочных строительных материалов осуществлялось методом динамического термогравиметрического анализа, а идентификация продуктов термического разложения отделочных строительных материалов – методом инфракрасной спектроскопии. Термический анализ проводился на приборе синхронного термического анализа NETZSCH STA 449 F3 Jupiter, позволяющем фиксировать изменение массы и величин теплового потока от температуры. Нагрев образцов осуществлялся со скоростью 10℃/мин в атмосфере воздуха с расходом 100 мл/мин в интервале температур 25℃-650℃. Образующиеся при термической деструкции газообразные продукты анализировались на ИК-Фурье спектрометре «ФСМ 1201» с газовой кюветой ТГА 100 при длинах волн 600-4500 см-1. По результатам исследования получены ТГ, ДТГ и ДСК-кривые, характеризующие соответственно потерю массы образца, скорость потери массы и изменение величины теплового потока от температуры, а также ИК-спектры продуктов термической деструкции отделочных строительных материалов при различных температурах. Установлено, что отделочные строительные материалы при их термической деструкции образуют различные химические соединения, отдельные из которых представляют опасность для организма человека. This article presents the results of experimental research on thermal destruction of finishing building materials and a hazard assessment of the process. Thermal destruction of finishing materials was investigated by thermal analysis and the risk of the process was assessed by infrared spectroscopy of gaseous products resulting from thermal destruction. The thermal analysis was carried out by dynamic thermogravimetric analysis on the synchronous thermal analysis instrument NETZSCH STA 449 F3 Jupiter, which makes it possible to detect changes in mass and heat flow from temperature. The heating of the samples was carried out at a rate of 10 ℃/min in the atmosphere with a consumption of 100 ml/min. The gaseous products formed during thermal destruction were analyzed by infrared spectroscopy on IR-Fourier spectrometer «FSM 1201» with gas cell TGA 100 at wavelengths of 600-4500 cm-1. The results of the study led to the production of TG, TFG and DSK curves, describing respectively the loss of sample mass, the rate of mass loss and the change of heat flow from temperature as well as infrared spectra of products of thermal destruction of finishing building materials at various temperatures. It has been found that the finishing building materials, when thermally disrupted, form various chemical compounds, some of which are dangerous to the human body.

Gut-Microbial Metabolites, Probiotics and Their Roles in Type 2 Diabetes

Type 2 diabetes (T2D) is a worldwide prevalent metabolic disorder defined by high blood glucose levels due to insulin resistance (IR) and impaired insulin secretion. Understanding the mechanism of insulin action is of great importance to the continuing development of novel therapeutic strategies for the treatment of T2D. Disturbances of gut microbiota have been widely found in T2D patients and contribute to the development of IR. In the present article, we reviewed the pathological role of gut microbial metabolites including gaseous products, branched-chain amino acids (BCAAs) products, aromatic amino acids (AAAs) products, bile acids (BA) products, choline products and bacterial toxins in regulating insulin sensitivity in T2D. Following that, we summarized probiotics-based therapeutic strategy for the treatment of T2D with a focus on modulating gut microbiota in both animal and human studies. These results indicate that gut-microbial metabolites are involved in the pathogenesis of T2D and supplementation of probiotics could be beneficial to alleviate IR in T2D via modulation of gut microbiota.

Resurgence of a Nation’s Radiation Science Driven by Its Nuclear Industry Needs

This article describes the radiation facilities and associated sample preparation, management, and analysis equipment currently in place at the Dalton Cumbrian Facility, a facility which opened in 2011 to support the UK’s nuclear industry. Examples of measurements performed using these facilities are presented to illustrate their versatility and the breadth of research they make possible. Results are presented from research which furthers our understanding of radiation damage to polymeric materials, radiolytic yield of gaseous products in situations relevant to nuclear materials, radiation chemistry in light water reactor cooling systems, material chemistry relevant to immobilization of nuclear waste, and radiation-induced corrosion of fuel cladding elements. Applications of radiation chemistry relevant to health care are also described. Research concerning the mechanisms of radioprotection by dietary carotenoids is reported. An ongoing open-labware project to develop a suite of modular sample handling components suited to radiation research is described, as is the development of a new neutron source able to provide directional beams of neutrons.

Comparative Studies on Thermal Decompositions of Dinitropyrazole-Based Energetic Materials

Dinitropyrazole is an important structure for the design and synthesis of energetic materials. In this work, we reported the first comparative thermal studies of two representative dinitropyrazole-based energetic materials, 4-amino-3,5-dinitropyrazole (LLM-116) and its novel trimer derivative (LLM-226). Both the experimental and theoretical results proved the active aromatic N-H moiety would cause incredible variations in the physicochemical characteristics of the obtained energetic materials. Thermal behaviors and kinetic studies of the two related dinitropyrazole-based energetic structures showed that impressive thermal stabilization could be achieved after the trimerization, but also would result in a less concentrated heat-release process. Detailed analysis of condensed-phase systems and the gaseous products during the thermal decomposition processes, and simulation studies based on ReaxFF force field, indicated that the ring opening of LLM-116 was triggered by hydrogen transfer of the active aromatic N-H moiety. In contrast, the initial decomposition of LLM-226 was caused by the rupture of carbon-nitrogen bonds at the diazo moiety.