The Influence of Nanoparticles on Fire Retardancy of Pedunculate Oak Wood

Traditional flame retardants often contain halogens and produce toxic gases when burned. Hence, in this study, low-cost, environmentally friendly compounds that act as fire retardants are investigated. These materials often contain nanoparticles, from which TiO2 and SiO2 are the most promising. In this work, pedunculate oak wood specimens were modified with sodium silicate (Na2SiO3, i.e., water glass) and TiO2, SiO2, and ZnO nanoparticles using the vacuum-pressure technique. Changes in the samples and fire characteristics of modified wood were studied via thermal analysis (TA), infrared spectroscopy (FTIR), and scanning electron microscopy, coupled with energy-dispersive X-ray spectroscopy (SEM-EDX). The results of TA showed the most significant wood decomposition at a temperature of 350 °C, with a non-significant influence of the nanoparticles. A dominant effect of sodium silicate was observed in the main weight-loss step, resulting in a drop in decomposition temperature within the temperature range of 36–44 °C. More intensive decomposition of wood treated with water glass and nanoparticles led to a faster release of non-combustible gases, which slowed down the combustion process. The results demonstrated that wood modifications using sodium silicate and nanoparticle systems have potentially enhanced flame retardant properties.

Fire Resistance of Steel Structures with Epoxy Fire Protection under Cryogenic Exposure

Cases of fire with highly flammable, combustible liquids and combustible gases with high potential heat emission at oil and gas facilities are assumed to develop as a hydrocarbon fire, which is characterized by the temperature rising rapidly up to 1093 ± 56 °C within five minutes from the test start and staying within the same range throughout the test, as well as by overpressure being generated. Although various fireproof coating systems are commonly used to protect steel structures from high temperatures, a combination of fire protection and cryogenic spillage protection, i.e., protection from liquefied natural gas (LNG), is rather an international practice novelty regulated by standards ISO 20088. Thanks to their outstanding features, i.e., ability to sustain chemical and climatic impact, these epoxy-based materials are able to ensure positive fireproof performance for steel structures in the case of potential cryogenic impact. The article discusses tests on steel structures coated with epoxy fireproof compounds, specifically PREGRAD-EP, OGRAX-SKE and Chartek 2218. The test records show the time from the start of cryogenic exposure to the said sample reaching the limit state, as well as the time from the start of heat impact to the sample reaching the limit state in case of hydrocarbon fire temperature.

Study on Gas-Generating Property of Lithium-Ion Batteries

A main cause of fires and explosions in lithium-ion batteries is the generation of combustible gases by them, and when a large number of batteries are densely packed, like in an Energy Storage System, there is a high risk of thermal runaway and fire propagation. Currently, many studies are being conducted worldwide to predict and prevent the generation of combustible gases, and thermal runaway in lithium-ion batteries, but they are still in progress. Therefore, in this study, we analyzed the gases generated before and after thermal runaway in lithium ion batteries, to prepare a basis for reducing the risk of thermal runaway. We aimed to establish the basis for prevention by early detection in the event of thermal runaway, by understanding the type and characteristics of the generated gases. For the experiment, lithium ion batteries were classified in terms of appearance (cylindrical, prismatic, pouch type), and cathode materials (NCM, NCA, LFP). The gases generated was measured against time. An FT-IR analyzer was used for gas measurement, and a separate hydrogen sensor was installed in the chamber to analyze changes in the types of gas, and measure the mass of the lithium ion battery over time. In the experiment, CO2 and CO were generated the most during thermal runaway in all lithium-ion batteries. Thereafter, CO2 increased, and CO decreased in the prismatic and pouch types, and both CO2 and CO increased in the cylindrical type. HF (a toxic gas), and H2 having a wide explosive range, were also generated, and the concentrations of these gases were inversely proportional to each other.

Effect of Woody Biomass Gasification Process Conditions on the Composition of the Producer Gas

Using woody biomass in thermochemical gasification can be a viable alternative for producing renewable energy. The type of biomass and the process parameters influence the producer gas composition and quality. This paper presents research on the composition of the producer gas from the gasification of three woody biomass species: spruce, alder, and pine. The experiments were conducted in a drop-tube reactor at temperatures of 750, 850, and 950 °C, using air as the gasifying agent, with equivalence ratios of 0.38 and 0.19. Gas chromatography with a thermal conductivity detector was used to determine the composition of the producer gas, while the production of total organic compounds was detected using Fourier-transform infrared spectroscopy. All three wood species exhibited very similar producer gas composition. The highest concentration of combustible gases was recorded at 950 °C, with an average of 4.1, 20.5, and 4.6 vol% for H2, CO, and CH4, respectively, and a LHV ranging from 4.3–5.1 MJ/m3. The results were in accordance with other gasification studies of woody species. Higher temperatures enhanced the composition of the producer gas by promoting endothermic and exothermic gasification reactions, increasing gas production while lowering solid and tar yields. The highest concentrations of combustible gases were observed with an equivalence ratio of 0.38. Continuous TOC measurement allowed understanding the evolution of the gasification process and the relation between a higher production of TOC and CO as the gasification temperature raised.

Nitrogen Gas Adsorption Filter (NgAF) to enhance producer gas quality

Biomass gasification is a thermochemical conversion process of solid biomass into a gaseous fuel called producer gas that can be used to generate power and electricity. The producer gas consists of around 47% of Nitrogen (N2), 24% Carbon Monoxide (CO), 16% Carbon Dioxide (CO2), 12% Hydrogen (H2), and 1% Methane (CH4). However, Nitrogen (N2) content in the producer gas reduces its heating values as N2 acts as a diluent because of the low calorific value (LCV) of gas. This study aims to design a Nitrogen gas filter for capturing nitrogen gas from producer gas to increase the heating value of producer gas as fuel in combustion. The method to increase the heating value of producer gas will increase the number of combustible gases or reduce the composition of non-combustible gases in producer gas. The use of material name zeolite with its microporous structures able to adsorb nitrogen molecules and act as catalysts to chemical reactions. Zeolites 5A have a small pore highly efficient to adsorb nitrogen gas because pore diameter is relatively similar to the size of nitrogen molecules. The quality of the producer gas depends on the design and operating parameters of the zeolite catalyst. Nitrogen Gas Adsorption Filter is a new method that has to be designed to improve the previous producer gas quality. Nitrogen Gas Adsorption Filter consists of a cylindrical shape body packed with crushed zeolites 5A. When this method of adsorption process is applied, the heating value of the producer gas is increased by observing the quantity of blue flame colour produced by NgAF.

Study on combustible gas generation and radionuclide release during underwater handling of the AM reactor spent fuel

Introduction. The paper addresses studies on the accumulation of combustible gases during underwater handling simulations for the leaky spent nuclear fuel from the AM reactor. Two fuel compositions were studied- uranium-molybdenum dispersed in magnesium and uranium carbide dispersed in calcium. Methods. The 137Cs release rate was measured during underwater storage of the uranium-molybdenum fuel. The kinetics of hydrogen release for both fuels and methane release for the carbide SNF were obtained. The kinetics approximate most with exponential dependences that formally correspond to first-order chemical reactions. A contribution of radiolytic hydrogen to the gases generated during the experiments was estimated. It was demonstrated that the determining source of the gases is the chemical interaction between the spent fuel and the water. The experiment with the uranium-molybdenum fuel demonstrated a pronounced passivation effect of the chemical processes on the fuel surface due to insoluble corrosion products. For the carbide SNF, an incubation period of about 20 hours was observed followed by an intensive release of hydrogen and methane. Results. The obtained results were subject to a comparative analysis against publications on the behavior of the fuel components in water. Conclusion. The findings can be applied to justify fire and explosion safety of underwater handling techniques for the damaged spent nuclear fuel with the considered fuel compositions (the spent fuel from reactors AM, AMB, EGP-6, etc.), e.g., to justify underwater preparations of the AMB spent fuel for reprocessing.

A phosphorus-containing hyperbranched phthalocyanine flame retardant for epoxy resins

A hyperbranched phosphorus-containing copper phthalocyanine compound (DOPO-CuPc) was successfully synthesized and used as the flame-retardant additive to prepare flame-retarded epoxy thermosets. The addition of DOPO-CuPc led to a significant enhancement of the flame retardant properties of the epoxy resin. The 15DOPO-CuPc/EP composite obtained a LOI value of 35.8%, and the UL-94 rose from NR to V-0 rating. And the addition of DOPO-CuPc resulted in early decomposition of the epoxy thermoset, but the residual char at 700 °C reached 27.7%. The flame retardant mechanism was further investigated. It was found that DOPO-CuPc could release phosphorus-containing radicals and non-combustible gases in the gas phase to exert gas-phase flame retardant activity. In the condensed phase, the epoxy thermoset formed the expanded honeycomb-like char layer during combustion and the presence of copper phthalocyanine contributed to the stability of the char layer.

Recapitulation and Prospect of Research on Flow Field in Coal Mine Gob

Coal mine gob, mined-out areas in underground coal mines, often accumulates explosive methane-air mixtures that pose a deadly hazard to miners. A good understanding of the flow field in a sealed coal mine area is crucial in preventing and minimizing accidents associated with mine combustible gases and also for planning and implementing a mine rescue strategy. In recent years, the research on the flow field in the gob has changed from qualitative research in the past to quantitative research. This paper synthesizes the research results of flow field in gob in recent 40 years, covering the permeability of quarried areas, the airflow simulation in quarried areas, and the influence of ventilation parameters and geohydrological conditions on the flow field. Firstly, the overburden failure mechanism and fracture development characteristics of the mine gob, the distribution of porosity and permeability in the gob, and the relationship between them are introduced. Secondly, the development of research methods and numerical models used to study the flow field in mine gob is discussed. The distribution of the flow field in the gob under different conditions is expounded. Thirdly, the research on the prevention and control of fire and explosion risks in the gob is discussed. Finally, the problems to be solved in such research direction are addressed and suggestions are put forward.