Law of variation for low density polyethylene dust explosion with different inert gases

To reveal the effects of different inert gases on explosion characteristics during low density polyethylene (LDPE) dust explosion and optimize the explosion-proof process, eight N₂ (CO₂)/air mixed inerting conditions were experimentally studied. Typical inerting conditions with 12 L cylindrical explosive tank were used to study the characteristics on the flame propagation. The thermogravimetric analysis with related theories were used to further explain the mechanism and quantities in low density polyethylene (LDPE) dust explosion with different inert gases. The results showed that the reduction of O₂ concentration could effectively delay the progress of flame growth process and weaken the effect of dust combustion reaction. The flame growth process of condition (N₂/air (18% O₂)) was 2.05 times slower than that of the non-inert condition. The explosion strength was obviously reduced, and the characteristic parameters such as explosion pressure and flame propagation speed were also affected by the decrease of O₂ concentration. For LDPE powder, the smaller the median diameter, the greater the explosion intensity and the lower the limiting oxygen content (LOC). The LOC with CO₂ was usually higher than that with N₂ and the effect of CO₂ was significantly better than N₂ in inerting.     

Effects of N2 and CO2 on the flammability of 2,3,3,3-tetrafluoropropene at elevated temperatures

The flammability characteristics of refrigerants are affected by environmental factors, making them prone to flammability and explosion accidents in cooling systems. In this paper, the flammability characteristics of R1234yf–air mixtures with N₂ and CO₂ were investigated comparatively at temperatures between 20 and 50 °C at 80% relative humidity. The lower and upper flammability limits of R1234yf were measured. The limiting oxygen concentration (LOC), critical flammable ratio (CFR), and critical flammable concentration (CFC) of the R1234yf–air mixtures with inert gases were investigated. The paper developed a linear formula between the flammability limit of R1234yf and the temperature. The changes in CFC with different temperatures were negligible for R1234yf. Furthermore, the mixed refrigerant had both non-flammability and the lowest vapor pressure when the CFR of the R1234yf/CO₂ mixture was 2.9. The experimental results were used to propose a new prediction model to estimate the flammability limits of R1234yf. Finally, molecular simulation explained the effect of inert gases on the flammability of R1234yf from a microscopic point of view. The research aimed to provide valid evidence and data for preventing flammable and explosive refrigerant incidents.     

Explosion regions of 1,3-dioxolane/nitrous oxide and 1,3-dioxolane/air with different inert gases - Experimental data and numerical modelling

In this study, experimental determination and modelling investigations for the explosion regions of 1,3-dioxolane/inert gas/N₂O and 1,3-dioxolane/inert gas/air mixtures were carried out and compared. The experimental measurements were carried out at 338 K and atmospheric pressure according to EN1839 method T using the inert gases N₂, CO₂, He and Ar. The results showed that the ratio of the lower explosion limit in N₂O (LEL_N2O) to the lower explosion limit in air (LEL_air) is 0.52 and the ratio of the maximum oxygen content in air (MOC_air) to the limiting oxidizer fraction in nitrous oxide (LOF_N2O) is 0.36 ± 0.02 independent of the inert gas. When comparing the inert gas amount at the apex based on the pure oxidizing component, which is O₂ in case of air, N₂O-containing mixtures need less inert gas to reach the limiting oxidizer quantity whereas the efficiency of inert gases is in the same order. The coefficients of nitrogen equivalency however were found to differ to some extent. The explosion regions of 1,3-dioxolane/inert gas/oxidizer mixtures were modelled using the calculated adiabatic flame temperature profile (CAFTP) method as well as corrected adiabatic flame temperatures. The results indicate good agreement with experimental data for CO₂, N₂ and Ar- containing mixtures. The noticeable deviations that occur when He is the inert gas are due to the lacking transport data of that mixture.     

Fire and Explosion Characteristics of 3-Methyl Pyridine at 270°C with High Oxygen Concentrations

The mixture of 3-methyl pyridine (3-picoline) and steam is used in the production of vitamin B3 in the gas phase. The aim of this study was to investigate the influence of inert steam (H₂O) on the flammability characteristics of 3-picoline in the manufacturing process. Four practical vapour mixing ratios of 3-picoline/steam mixtures, 5, 10, 30 and 100 vol% 3-picoline, were selected in this study. A series of flammability tests were employed for determining their fire and explosion characteristics. Fire tests H₂O: 3-picoline 5,10, 30 and 100 vol% were carried out in a 20-L-Apparatus under simulated conditions of 760 mmHg, 270°C, together with high oxygen concentrations (42 and 21 vol%) used in the real process.The experimental results showed that the safety-related parameters and flammability hazard degrees were all able to be significantly reduced while substantial amount of steam was infused into the 3-picoline/steam system. While the steam proportion was up to 97 vol%, 3-picoline/steam would be non-flammable. As a result, dosing steam to the process is one of the effective methods to prevent the relevant processes from incurring fire and explosion hazards, not to mention its economical benefit.     

Coupling effects of venting and inerting on explosions in interconnected vessels

The coupling effects of venting and CO₂ inerting on stoichiometric methane-air mixture explosions were investigated in an isolated vessel and interconnected vessels. The results indicate that venting mitigates the explosion intensity, especially for small vessels. For vessels connected by pipes, a venting design following EN 14994 (2007) and NFPA 68 (2013) could not meet the venting requirements. For an isolated big vessel and interconnected vessels, increasing the CO₂ volume fraction (Φ) from 0 to 15.0 vol% decreased the maximum explosion overpressure (P_max) and maximum rate of overpressure rise ((dP/dt)_max) and delayed t_max. For closed interconnected vessels, P_max varied approximately linearly with Φ. For both isolated vessel and interconnected vessels, the coupling effects of venting and CO₂ inerting on methane-air explosion were more efficient than those of individual mitigative method (that is, venting alone or CO₂ inerting alone).     

Inerting characteristics of ultrafine Mg(OH)2 on starch dust explosion flame propagation

Experiments on the flame propagation of starch dust explosion with the participation of ultrafine Mg(OH)₂ in a vertical duct were conducted to reveal the inerting evolution of explosion processes. Combining the dynamic behaviors of flame propagation, the formation law of gaseous combustion products, and the heat dissipation features of solid inert particles, the inerting mechanism of explosion flame propagation is discussed. Results indicate that the ultrafine of Mg(OH)₂ powders can cause the agglomeration of suspended dust clouds, which makes the flame combustion reaction zone fragmented and forms multiple small flame regions. The flame reaction zone presents non-homogeneous insufficient combustion, which leads to the obstruction of the explosion flame propagation process and the obvious pulsation propagation phenomenon. As the proportion of ultrafine Mg(OH)₂ increases, flame speed, flame luminescence intensity, flame temperature and deflagration pressure all show different degrees of inerting behavior. The addition of ultrafine Mg(OH)₂ not only causes partial inerting on the explosion flame, but also the heat dissipation of solid inert particles affects the acceleration of its propagation. The explosion flame propagation is inhibited by the synergistic effect of inert gas-solid phase, which attenuates the risk of starch explosion. The gas-solid synergistic inerting mechanism of starch explosion flame propagation by ultrafine Mg(OH)₂ is further revealed.     

Inhibiting effects of gas–particle mixtures containing CO2, Mg(OH)2 particles,and NH4H2PO4 particles on methane explosion in a 20-L closed vessel

The main risk factors from methane explosion are the associated shock waves, flames, and harmful gases. Inert gases and inhibiting powders are commonly used to prevent and mitigate the damage caused by an explosion. In this study, three inhibitors (inert gas with 8.0 vol% CO₂, 0.25 g/L Mg(OH)₂ particles, and 0.25 g/L NH₄H₂PO₄ particles) were prepared. Their inhibiting effects on methane explosions with various concentrations of methane were tested in a nearly spherical 20-L explosion vessel. Both single-component inhibitors and gas–particle mixtures can substantially suppress methane explosions with varying degrees of success. However, various inhibitors exhibited distinct reaction mechanisms for methane gas, which indicated that their inhibiting effects for methane explosion varied. To alleviate amplitude, the ranking of single-component inhibitors for both explosion pressure (P_ex) and the rate of explosion pressure rise [(dP/dt)_ex] was as follows: CO₂, NH₄H₂PO₄ particles, and Mg(OH)₂ particles. In order of decreasing amplitude, the ranking of gas‒particle mixtures for both P_ex and (dP/dt)_ex was as follows: CO₂–NH₄H₂PO₄ mixture, CO₂‒Mg(OH)₂ mixture, and pure CO₂. Overall, the optimal suppression effect was observed in the system with the CO₂–NH₄H₂PO₄ mixture, which exhibited an eminent synergistic effect on methane explosions. The amplitudes of P_ex with methane concentrations of 7.0, 9.5, and 11.0 vol% decreased by 37.1%, 42.5%, and 98.6%, respectively, when using the CO₂–NH₄H₂PO₄ mixture. In addition, an antagonistic effect was observed with CO₂‒Mg(OH)₂ mixtures because MgO, which was generated by the thermal decomposition of Mg(OH)₂, can chemically react with water vapor and CO₂ to produce basic magnesium carbonate (xMgCO₃·yMg(OH)₂·zH₂O), thereby reducing the CO₂ concentration in a reaction system. This research revealed the inhibiting effects of gas‒particle mixtures (including CO₂, Mg(OH)₂ particles, and NH₄H₂PO₄ particles) on methane explosions and provided primary experimental data.     

Inhibiting effects by Fe2O3 on combustion and explosion characteristics of ABS resin

The global increase in the use of, and reliance on, plastics has prompted the demand for acrylonitrile-butadiene-styrene (ABS) resin in various fields. With this increased requirement, numerous failures have occurred in the ABS process. Those incidents, resulting from electrostatic discharge, powder accumulation, heat accumulation, construction sparks, and plant fires, have caused dust fire and explosions.In this study, the ABS resin was gleaned from the site and tested for its explosion parameters, including minimum ignition temperature of dust cloud (MIT_C), minimum ignition energy (MIE), and minimum explosion concentration (MEC). To improve loss prevention in the manufacturing process, ferric oxide (Fe₂O₃) as an inert additive was added in the ABS powder. According to the MIE test, Fe₂O₃ has an apparent inhibiting effect on dust explosion for the ABS dust. With the proportion of Fe₂O₃ increased from 25 to 50 mass% in ABS, the MIE increased from 67 to 540 mJ. The explosion tests via 20-L apparatus indicated that Fe₂O₃ mixed with ABS could not increase the MEC significantly. However, the explosion pressure dropped by increasing in the ratio of Fe₂O₃ in ABS. This inerting strategy of ABS was deemed to substantially lessen the probability and severity of fire and explosion.     

Experiment-based investigations of magnesium dust explosion characteristics

An experimental investigation was carried out on magnesium dust explosions. Tests of explosion severity, flammability limit and solid inerting were conducted thanks to the Siwek 20 L vessel and influences of dust concentration, particle size, ignition energy, initial pressure and added inertant were taken into account. That magnesium dust is more of an explosion hazard than coal dust is confirmed and quantified by contrastive investigation. The Chinese procedure GB/T 16425 is overly conservative for LEL determination while EN 14034-3 yields realistic LEL data. It is also suggested that 2000-5000 J is the most appropriate ignition energy to use in the LEL determination of magnesium dusts, using the 20 L vessel. It is essential to point out that the overdriving phenomenon usually occurs for carbonaceous and less volatile metal materials is not notable for magnesium dusts. Trends of faster burning velocity and more efficient and adiabatic flame propagation are associated with fuel-rich dust clouds, smaller particles and hyperbaric conditions. Moreover, Inerting effectiveness of CaCO₃ appears to be higher than KCl values on thermodynamics, whereas KCl represents higher effectiveness upon kinetics. Finer inertant shows better inerting effectiveness.     

Inerting effect of N2 on explosion of LDPE dust/ethylene hybrid mixtures

Explosion flame propagation characteristics and overpressure distribution of low density polyethylene (LDPE) dust and ethylene hybrid mixture were investigated under N₂ inerting conditions using a custom-designed 12 L cylindrical explosion tank. The results showed that a small amount of ethylene could promote the explosion characteristics of LDPE dust. N₂ inerting had different inhibitory effects on the explosion flame of LDPE dust and its mixture with ethylene. The explosion overpressure strength of the LDPE dust/ethylene hybrid mixture decreased with increasing N₂ concentration. The overall suppression effect of N₂ on the explosion overpressure of the LDPE dust was better than that of the LDPE dust/ethylene hybrid mixture explosion. As the ethylene concentration increased from 0% to 2.5%, the limiting oxygen concentration decreased by 13% oxygen. This small amount of ethylene restricted the traditional inerting process. The study conclusions can provide further scientific basis for the inerting and explosion proofing design of production process equipment involving LDPE dust.     

Lower flammability limits of flammable ternary organic mixtures: Synergistic behavior

Organic flammable liquids and their mixtures, which possess high risk of combustion and explosion, are widely used as raw materials and solvents in chemical and pharmaceutical industries. Lower flammability limits (LFL) is one of the most important parameters to characterize the combustion and explosion hazards of combustible gases and liquid vapors. The LFL of various ternary organic mixtures consist of ketone (acetone and butanone), ester (ethyl acetate) and alcohol (ethanol and isopropanol) were tested at 25 °C and atmospheric pressure. The results showed that resulted LFL values of the experiment were always lower than those calculated by volume fraction weighting method when the volume fraction of alcohol was less than 20 vol% but more than 10 vol%. The co-existence of alcohol and ethyl acetate had synergistic effect on reducing the LFL values of ternary organic mixtures and thus increased their explosive risk. The mechanism of synergistic effect was analyzed, and the results showed that the OH· and H· radicals produced by the oxidation decomposition of alcohols and esters accelerated the oxidation process of ternary organic mixtures, which led to the decrease of experimental LFL values and thus corresponding increased of their explosive risk. This study would be expected to provide some guidance for designing or choosing safer and more suitable ternary organic mixtures prior to their applications for engineering.     

Inerting effect of CaCO3 powder on flame spread of wood dust layer

The effect of CaCO₃ powder, a typical inert dust, on the flame spread characteristics of wood dust layers was studied using an experimental device to understand the ignition characteristics of and develop inert explosion-proof technology for deposited wood dust. The results showed that the flame spread velocity (FSV) of the mixed dust layer was affected by the dispersion effect of CaCO₃ powder and physical heat absorption. As the CaCO₃ powder mass fraction increased, the FSV of the dust layer first increased and then decreased, reaching a peak at a 50% mass fraction. Moreover, the front-end temperature of the flame gradually decreased, and the red spark faded. The combustion reaction of the mixed dust layer could be more completed, and the colour of the combustion residue changed from charcoal black to charcoal grey. The coupling effect of the initial temperature and wind speed can promote an increase in the FSV in the mixed dust layer. The Gauss–Amp model of the FSV of the wood dust layer and mass fraction of CaCO₃ powder showed that the peak of the FSV occurred when the mass fraction of CaCO₃ powder was between 40 and 50%. Thus, a good inerting and explosion-proof effect can be achieved by using CaCO₃ powder with a mass fraction of more than 50%; it can improve the whole inerting process. Inert explosion-proof technology should be considered when assessing fire and explosion risk of dust in real process industry situations.     

Effects of initial temperature and pressure on explosion characteristics of propane–diluent–air mixtures

The explosion characteristics of propane–diluent–air mixtures under various temperatures and pressures were investigated using a 20-L apparatus. The explosion limits of propane diluted with nitrogen or carbon dioxide were measured at high temperatures from 25 to 120 °C. The results showed that the upper explosion limit (UEL) increased, and the lower explosion limit (LEL) decreased with the rising temperature. The explosion limits of propane diluted with nitrogen or carbon dioxide were also measured at high pressures from 0.10 to 0.16 MPa. The results showed that the UEL increased, and the LEL almost remainedunchanged along with increased pressure. Under the same initial operating conditions, the concentration of nitrogen required to reach the minimum inerting concentration (MIC) point was higher than the concentration of carbon dioxide. Finally, the study investigated the limiting oxygen concentration (LOC) of propane under various initial temperatures, initial pressures, and inert gases. The LOC of propane decreased approximately linearly with increased temperature or pressure, and the LOC of propane dilution with carbon dioxide was greater than dilution with nitrogen from 25 to 120 °C or from 0.10 to 0.16 MPa, which indicated that the dilution effect of carbon dioxide was better than that of nitrogen.     

Minimum ignition energies of pure magnesium powders due to electrostatic discharges and nitrogen's effect

This paper experimentally investigated the relation between the minimum ignition energy (MIE) of magnesium powders as well as the effect of inert nitrogen (N₂) on the MIE. The modified Hartmann vertical-tube apparatus and four kinds of different-sized pure magnesium powders (median particle size, D50; 28.1 μm–89.8 μm) were used in this study. The MIE of the most sensitive magnesium powder was 4 mJ, which was affected by the powder particle size (D50; 28.1 μm). The MIE of magnesium powder increased with an increase in the N₂ concentration for the inerting technique. The magnesium dust explosion with an electrostatic discharge of 1000 mJ was suppressed completely at an N₂ concentration range of more than 98%. The experimental data presented in this paper will be useful for preventing magnesium dust explosions generated from electrostatic discharges.     

The influence of inert gas on limiting experimental safe gap of fuel-air mixtures at various initial pressures

The Maximum Experimental Safe Gap (MESG) is an important criterion to assess the propagation of flames through small gaps. This safety-related parameter is used to classify the flammable gases and vapors in explosion groups, which are fundamental to constructional explosion protection. It is used both, for the safe design of flameproof encapsulated devices as well as for selecting flame arresters appropriate to the individual application. The MESG of a fuel is determined experimentally according to the standard ISO/IEC 80079-20-1:2017 at normal conditions (20 °C, 1.0 bar) with air as oxidizing gas. The aim of this work is to investigate the effect of inert gas addition on the MESG in order to assess the effectiveness of inertization in constructional explosion protection. The term limiting experimental safe gap (S_G) is used for the result of these measurements. The fuel-air mixtures (fuels: hydrogen, ethylene, propene, methane) used as representatives for the explosion groups in flame arrester testing were chosen and diluted with inert gas (nitrogen, carbon dioxide) before testing. The dependence of the limiting experimental safe gap on the total initial pressure, amount and nature of inert additive is discussed. The initial pressure was varied up to 2.0 bar to include increased pressure conditions used in flame arrester testing. Apart from the well-known reciprocal dependence on the initial pressure, the added inert gas results in an exponential increase of S_G. This effect depends on the inertizing potential of the gas and is therefore different with nitrogen and carbon dioxide. The ranking of the fuels is the same as with MESG. As a result, various mixtures of the same limiting experimental safe gap can now be chosen and tested with an individual flame arrester to prove the concept of a constant and device-related limiting safe gap. The work was funded by BG-RCI in Heidelberg (PTB grant number 37056).     

Effect of Al2O3 particle size reduction on aluminium dust explosion

To investigate the effect of Al₂O₃ particle size on an aluminum explosion, the overpressure and flame velocity in a vertical duct were evaluated. The results show that the inhibitory effect of submicron Al₂O₃ is best, while the inhibitory effect increases with increasing inerting ratio. However, the inhibitory effect of micron Al₂O₃ does not increase significantly after the inerting ratio exceeds 40%. For high-concentration aluminum powder, 0.8 μm Al₂O₃ with an inerting ratio less than 20% promotes aluminum explosion. As the inerting ratio increases beyond 20%, however, the overpressure decreases. Furthermore, Al₂O₃ inhibits the formation of the intermediate product AlO and decreases the flame brightness. As the inerting ratio of 0.8 μm Al₂O₃ reaches 50%, the white patches in the flame image disappear. The results of scanning electron microscopy showed that the explosion products agglomerate and some dot-like protrusions appear on the surface of the unburned aluminum particles. The inhibition mechanism was qualitatively investigated. Physical heat absorption is proven to play a limited role. Thermal radiation and chemical inhibition play a key role. The chemical effect mainly influences the surface reaction energy source.     

Inerted vessels: Avoiding hazards caused by gas buoyancy

Performing hot work on a process vessel that previously contained a flammable hydrocarbon liquid poses a significant explosion and fire hazard. To reduce the combustion hazard potential, the facility operator may choose to purge and blanket the vessel with an inert gas such as nitrogen or carbon dioxide. Numerous accidents have occurred during hot work due to inadequate inerting operations. Oftentimes the source of the problem was inadequate gas composition control caused by gas buoyancy.A useful paradigm for analyzing the inerting process is the well-stirred control volume with a spatially uniform chemical composition (i.e., perfect mixing). Certain features of the vessel construction, in concert with the physical properties of the inert gas, can interfere with the complete mixing of the inert gas with the vessel atmosphere. This paper discusses how to evaluate the potential for buoyant flows to disrupt and interfere with the design goal of perfect mixing. Three case studies of accident investigations are used to illustrate the potentially detrimental effects of buoyancy on inerting operations. Finally, recommendations are presented on how to use buoyancy to improve the effectiveness of inerting operations.     

Flammability of hydrocarbon and carbon dioxide mixtures

The effect of carbon dioxide (CO₂) concentration on the ignition behaviour of hydrocarbon and CO₂ gas mixtures is examined in both jets and confined explosions. Results from explosion tests are presented using a 20 l explosion sphere and an 8 m long section of 1.04 m diameter pipeline. Experiments to assess the flame stability and ignition probability in free-jets are reported for a range of different release velocities. An empirically-based flammability factor model for free-jets is also presented and results are compared to ignition probability measurements previously reported in the literature and those resulting from the present tests.The results help to understand how CO₂ changes the severity of fires and explosions resulting from hydrocarbon releases. They also demonstrate that it is possible to ignite gas mixtures when the mean concentration is outside the flammable range. This information may be useful for risk assessments of offshore platforms involved in carbon sequestration or enhanced oil recovery, or in assessing the hazards posed by poorly-inerted hydrocarbon processing plant.     

The investigation of correlated factors of external explosion during the venting process

Experimental investigations were done in the paper for the process of venting explosion in a ϕ200 mm×400 mm cylindrical vessel. Compared with the normal venting process, the phenomenon of external explosion was observed and discussed first. Moreover, when CH₄–air mixture gases were used and the vent diameter was 55 mm, three kinds of condition were selected: ϕ=0.8, ϕ=1.0 and ϕ=1.3. And two ignition positions were selected: at the vessel center and at the bottom. Then the venting processes influenced by these factors were experimented and discussed, too.     

Experimental study on the minimum explosion concentration of anthracite dust: The roles of O2 mole fraction,inert gas and CH4 addition

The explosion characteristics of anthracite coal dust with/without small amount of CH₄ (1.14 vol %) were investigated by using a 20 L spherical explosion apparatus with an emphasis on the roles of oxygen mole fraction and inert gas. Two methods based on overpressure and combustion duration time were used to determine the minimum explosion concentration (MEC) or the lower explosion limit (LEL) of the pure anthracite coal dust and the hybrid coal-methane mixtures, respectively. The experiment results showed that increasing oxygen mole fraction increases the explosion risk of coal dust: with increasing oxygen mole fraction, the explosion pressure (P_ex) and the rate of explosion pressure rise ((dp/dt)_ex)) increase, while MEC decreases. The explosion risk of anthracite dust was found to be lower after replacing N₂ with CO₂, suggesting that CO₂ has a better inhibition effect on explosion mainly due to its higher specific heat. However, the addition of 1.14% CH₄ moderates the inhibition effect of CO₂ and the promotion effect of O₂ on anthracite dust explosion for some extent, increasing explosion severity and reducing the MEC of anthracite dust. For hybrid anthracite/CH₄ mixture explosions, Barknecht's curve was found to be more accurate and conservative than Chatelier's line, but neither are sufficient from the safety considerations. The experimental results provide a certain help for the explosion prevention and suppression in carbonaceous dust industries.