Effect of initial pressure on explosion characteristics of 2, 3, 3, 3–tetrafluoropropene

With the popularity of refrigerants in the process industries, the potential safety problems caused by the use of refrigerants have attracted worldwide attention as people have realized their inherent explosion characteristics of refrigerants. This paper studied the explosion characteristics of refrigerant 2, 3, 3, 3–tetrafluoropropene (R1234yf) at different concentrations and initial pressures based on a 20 L experimental apparatus. The experimental results illustrated the peak overpressure of R1234yf increased with the rise of initial pressure. At a constant ambient temperature of 25 °C, the maximum rate of pressure rise and deflagration index showed an N-shaped trend with the increase of the refrigerant concentration from 6.8% to 10%. The maximum rate of pressure rise and deflagration index increased first and then decreased with the increase of the refrigerant concentration at atmospheric pressure, while they presented an M-shaped trend at pressurization condition. The peak overpressure, the maximum rate of pressure rise, and deflagration index reached 0.742 MPa, 4.04 MPa s⁻¹, and 1.1 MPa.m.s⁻¹ with a refrigerant concentration of 7.6%, respectively, which were less than those of refrigerant propane and difluoromethane (R32) at the optimal concentration. Furthermore, R1234yf exhibited better safety performance compared with refrigerant R32 in the same flammability classification.     

Effect of initial temperature on explosion characteristics of 2, 3, 3, 3–Tetrafluoropropene

The flammability of refrigerants is a major cause of refrigerant explosion incidents. Studying the explosion characteristics of refrigerants at different initial temperatures can provide significant benefits for solving the safety problems of refrigerants under actual working conditions. This paper studied the effects of the initial temperature and refrigerant concentration on the explosion characteristics of refrigerant 2, 3, 3, 3-tetrafluoropropene (R1234yf) at 0.1 MPa. The curves of explosion characteristics with different initial temperature revealed the same variation trend ranged from 25 °C to 115 °C. Specifically, as the refrigerant concentration was raised, the peak overpressure, the maximum rate of pressure rise, and laminar burning velocity increased initially and decreased afterwards, along with maximum values at the refrigerant concentration of 7.6%. When the refrigerant concentration was 7.6%, the peak overpressure declined exponentially with the initial temperature rise, while the maximum rate of pressure rise increased linearly. The laminar burning velocity calculated from the spherical expansion method indicated that the flame propagation was gradually accelerated by the increase of initial temperature, which coincided with the change of the maximum rate of pressure rise. Meanwhile, experiments and CHEMKIN simulation results demonstrated the effects of elevated temperature from 20 °C to 50 °C on the explosion limits of R1234yf. The lower explosion limit reduced and the upper explosion limit increased with rising initial temperature. In general, R1234yf exhibited moderate combustion and lower explosion risk, compared with traditional refrigerants.     

竖直分支管道泄爆开启压力对甲烷爆燃压力的影响研究

针对市政排污管网等典型受限空间内可燃气体爆燃风险,建立由水平管道和竖直分支管道构成的数值模型,研究竖直分支管道不同泄爆开启压力对甲烷爆燃压力的影响.研究结果表明:不同泄爆开启压力条件下,管道内存在爆燃压力积聚和泄放的双重效应;水平管道内各测点压力时程曲线均表现为先增大后减小而后出现亥姆霍兹振荡,随着与爆源距离的增加,初...     

Comparative assessment of the explosion characteristics of alcohol–air mixtures

Explosion characteristics of five alcohol–air (ethanol, 1-butanol, 1-pentanol, 2-pentanol and 3-pentanol) mixtures were experimentally conducted in an isochoric chamber over wide ranges of initial temperature and pressure. The effect of temperature and pressure on the different explosion behaviors among these alcohols with various structures were investigated. Results show that the peak explosion pressure is increased with the decrease of temperature and increase of pressure. Maximum rate of pressure rise is insensitive to the temperature variation while it significantly increases with the increase of initial pressure. Among the 1-, 2-, and 3-pentanol–air mixtures, 1-pentanol has the highest values in peak explosion pressure and maximum rate of pressure rise and 2-pentanol gives the lowest values at the initial pressure of 0.1 MPa. These differences tend to be decreased with the increase of initial pressure. Among the three primary alcohol–air (ethanol, 1-butanol and 1-pentanol) mixtures, a similar explosion behavior is presented at the lean mixture side because of the combined effect of adiabtic temperature and flame propagation speed. At the rich mixture side, 1-pentanol gives the highest values in peak explosion pressure and maximum rate of pressure rise and ethanol gives the lowest values. This phenomenon can be interpretated from the combining influence of heat release and heat loss, since the flame speeds of ethanol-, 1-butanol-, 1-pentanol–air mixtures are close at rich mixture side.     

条形障碍物对瓦斯爆炸特性影响研究

我国煤矿瓦斯爆炸事故不断出现,造成了巨大的人员伤亡和经济损失,在置障条件下研究瓦斯爆炸特性,对预防和减少瓦斯爆炸事故具有重要意义。利用水平管道式爆炸试验装置,研究密闭管道内条形障碍物的数量和阻塞率对管道内瓦斯最大爆炸压力、火焰速度、最大爆炸压力上升速率和爆炸指数的影响以及敞口状态的影响。研究表明:障碍物对瓦斯爆炸具有显著激励作用,管道内瓦斯最大爆炸压力、火焰速度、最大爆炸压力上升速率和爆炸指数均显著增大,随着障碍物数量和阻塞率的增加,激励作用越明显;敞口状态下管道内最大爆炸压力、最大爆炸压力上升速率和爆炸指数均显著减小,火焰持续传播。研究结果对防治煤矿瓦斯爆炸事故提供一定的理论支持。     

Effects of nitrogen and carbon dioxide on hydrogen explosion behaviors near suppression limit

By varying inert gas content, equivalence ratio and initial pressure, this study is aimed at investigating flame propagation behaviors and explosion pressure characteristics near suppression limit. For carbon dioxide, the weakest flame floating phenomenon is observed at Φ = 1.5 and the buoyant instability is enhanced when the equivalent ratio deviates to the rich and lean sides. For nitrogen, the buoyant instability decreases with increasing equivalent ratio. Both maximum explosion pressure and maximum pressure rise rate increase firstly and then decrease with the increase of equivalence ratio, and they decrease significantly with increasing content of carbon dioxide and nitrogen. For carbon dioxide, the critical suppression ratio of Φ = 0.6, 0.8, 1.0, 1.5 and 2.0 is 7.50, 7.18, 5.74, 3.83, and 2.87. For nitrogen, the critical suppression ratio of Φ = 0.6, 0.8, 1.0, 1.5 and 2.0 is 15.83, 11.87, 9.50, 6.33 and 4.75. Compared to nitrogen, the carbon dioxide is more effective on suppressing hydrogen explosion pressure. The adiabatic flame temperature, thermal diffusivity and mole fraction of active radicals continue to decrease with increasing content of carbon dioxide and nitrogen, which contributes to the decrease of laminar burning velocity.     

Laminar burning velocities of hydrogen–air mixtures from closed vessel gas explosions

The laminar burning velocity of hydrogen–air mixtures was determined from pressure variations in a windowless explosion vessel. Initially, quiescent hydrogen–air mixtures of an equivalence ratio of 0.5–3.0 were ignited to deflagration in a 169 ml cylindrical vessel at initial conditions of 1 bar and 293 K. The behavior of the pressure was measured as a function of time and this information was subsequently exploited by fitting an integral balance model to it. The resulting laminar burning velocities are seen to fall within the band of experimental data reported by previous researchers and to be close to values computed with a detailed kinetics model. With mixtures of an equivalence ratio larger than 0.75, it was observed that more advanced methods that take flame stretch effects into account have no significant advantage over the methodology followed in the present work. At an equivalence ratio of less than 0.75, the laminar burning velocity obtained by the latter was found to be higher than that produced by the former, but at the same time close enough to the unstretched laminar burning velocity to be considered as an acceptable conservative estimate for purposes related to fire and explosion safety. It was furthermore observed that the experimental pressure–time curves of deflagrating hydrogen–air mixtures contained pressure oscillations of a magnitude in the order of 0.25 bar. This phenomenon is explained by considering the velocity of the burnt mixture induced by the expansion of combusting fluid layers adjacent to the wall.     

Effects of hydrogen addition on the confined and vented explosion behavior of methane in air

Multi-component gas mixture explosion accidents occur and recur frequently, while the safety issues of multi-component gas mixture explosion for hydrogen–methane mixtures have rarely been addressed.Numerical simulation study on the confined and vented explosion characteristics of methane-hydrogen mixture in stoichiometric air was conducted both in the 5 L vessel and the 64 m³ chamber, involving different mixture compositions and initial pressures. Based on the results and analysis, it is shown that the addition of hydrogen has a negative effect on the explosion pressure of methane-hydrogen mixture at adiabatic condition. While in the vented explosion, the addition of the hydrogen has a significant positive effect on the explosion hazard degree. Additionally, the addition of hydrogen can induce a faster reactivity and enhance the sensitivity of the mixture by reducing the explosion time and increasing the rate of pressure rise both in confined and vented explosion. Both the maximum pressure and the maximum rate of pressure rise increase with initial pressure as a linear function, and also rise with the increase of hydrogen content in fuel. The increase in the maximum rate of pressure rise is slight when hydrogen ratio is lower than 0.5, however, it become significant when hydrogen ratio is higher than 0.5. The maximum rate of pressure rise for stoichiometric hydrogen-air is about 10 times the one of stoichiometric methane-air.Furthermore, the vent plays an important role to relief pressure, causing the decrease in explosion pressure and rate of pressure rise, while it can greatly enhance the flame speed, which will extend the hazard range and induce secondary fire damages. Additionally it appears that the addition of hydrogen has a significant increasing effect on the flame speed. The propagation of flame speed in confined explosion can be divided into two stages, increase stage and decrease stage, higher hydrogen content, higher slope. But in the vented explosion, the flame speed keeps increasing with the distance from the ignition point.     

Explosion parameters of wood chip-derived syngas in air

The wood gasification process poses serious concerns about the risk of explosion. The design of prevention and mitigation measures requires the knowledge of safety parameters, such as the maximum explosion pressure, the maximum rate of pressure rise and the gas deflagration index, K_G, at standard ambient temperature (25 °C) and pressure (1 bar) conditions. However, the analysis at specific process conditions is strongly recommended, as the explosion behavior of gas mixtures may be completely different.In the work presented in this paper, the explosion behavior of mixtures with composition representative of wood chip-derived syngas (CO/H₂/CH₄/CO₂/N₂ mixtures with and without H₂O) was experimentally studied in a closed combustion chamber. Experiments were run at two temperatures, 300 °C and 10 °C, and at atmospheric pressure. Test conditions were requested by the safety engineering designer of an existing industrial-scale wood gasification plant. In order to identify the specific fuel–air ratios to be analyzed, thus reducing the number of experimental tests, a preliminary thermo-kinetic study was performed.Results have shown that the mixtures investigated can be classified as low-reactivity mixtures, the higher value of K_G found (∼36 bar m/s) being much lower than the K_G value of methane (55 bar m/s @ 25 °C).     

Experimental study on CO2/CF3I suppression of methane-air explosion and flame propagation

To explore the inhibitory effects of CF₃I and CO₂ gas on the explosion pressure and flame propagation characteristics of 9.5% methane, a spherical 20 L experimental explosion device was used to study the effect of the gas explosion suppressants on the maximum explosion pressure, maximum explosion pressure rise rate and flame propagation speed of methane. The results indicated that with a gradual increase in the volume fraction of the gas explosion suppressant, the maximum explosion pressure of methane and maximum explosion pressure rise rate gradually decreased, and the time taken to reach the maximum explosion pressure and maximum explosion pressure rise rate was gradually delayed. At the same time, the flame propagation speed gradually decreased. Additionally, the time taken for the flame to reach the edge of the window and the time taken for a crack as well as a cellular structure to appear on the flame surface was gradually delayed. The fluid dynamics uncertainty was suppressed. The explosion pressure and flame propagation processes were markedly suppressed, but the flame buoyancy instability was gradually enhanced. By comparing the effects of the two gas explosion suppressants on the pressure and flame propagation characteristics, it was found that at the same volume fraction, trifluoroiodomethane was significantly better than carbon dioxide in suppressing the explosion of methane. By comparing the reduction rates of the characteristic methane explosion parameters at a volume fraction of 9.5%, it was observed that the inhibitory effect of 4% trifluoroiodomethane on the maximum explosion pressure was approximately 4.6 times that of the same amount of carbon dioxide, and the inhibitory effect of 4% trifluoroiodomethane on the maximum explosion pressure rise rate and flame propagation speed was approximately 2.7 times that of the same amount of carbon dioxide. The addition of 0.5%–1.5% trifluoromethane to 4% and 8% carbon dioxide can improve the explosion suppression efficiency of carbon dioxide. This enhancing phenomenon is a comprehensive manifestation of the oxygen-decreasing effect of carbon dioxide and the trifluoroiodomethane-related endothermic effect and reduction in key free radicals.     

缝洞型管道瓦斯爆炸特性数值模拟研究

为探究采空区遗煤、松散破碎岩块对瓦斯爆炸的影响,建立缝洞型管道模型,采用数值模拟与理论分析结合方法研究采空区内缝洞型管道内瓦斯爆炸的传播规律及管道长径比对瓦斯爆炸过程中速度与冲击波的影响。研究结果表明:在缝洞型结构内,随着火焰沿管道向前传播,各监测点速度逐渐变大、压力先增加后降低,而压力上升速率则表现出不规则的变化;缝洞结构加剧了火焰燃烧的剧烈程度,提高了管道内各监测点的温度峰值;在缝洞型管道内随长径比r增加,各监测点最大压力峰值以及速度大小依次降低。     

Study of the severity of hybrid mixture explosions and comparison to pure dust-air and vapour-air explosions

The explosion behaviour of heterogeneous/homogeneous fuel-air (hybrid) mixtures is here analysed and compared to the explosion features of heterogeneous fuel-air and homogeneous fuel-air mixtures separately.Experiments are performed to measure the pressure history, deflagration index and flammability limits of nicotinic acid/acetone-air mixtures in a standard 20 L Siwek bomb adapted to vapour-air mixtures. Literature data are also used for comparison.The explosion tests performed on gas-air mixtures in the same conditions as explosion tests of dust-air mixtures, show that the increase in explosion severity of dust/gas-air mixtures has to be addressed to the role of initial level of turbulence prior to ignition.At a fixed value of the equivalence ratio, by substituting the dust to the flammable gas in a dust/gas-air mixture the explosion severity decreases. Furthermore, the most severe conditions of dust-gas/air mixtures is found during explosion of gas-air mixture at stoichiometric concentration.     

Interaction of flame instabilities and pressure behavior of hydrogen-propane explosion

The flame destabilization mechanism of hydrogen-propane-air mixture is firstly revealed. The effects of unstable flame formation on pressure rise rate and burning rate are quantified. Finally, the theoretical prediction of explosion pressure behavior is performed by considering diffusive-thermal and hydrodynamic instability. The results demonstrated that before the explosion pressure starts to climbe, as the propane fraction increases, the effective Lewis number of lean and stoichiometric mixture undergoes the transition from Le_eff < 1.0 to Le_eff > 1.0, the stabilizing effect of diffusive-thermal instability continues to reduce for the rich mixture. After the explosion pressure starts to climbe, the hydrogen-propane flame becomes more unstable, which is mainly attributed to enhancing hydrodynamic instability. The maximum rate of pressure rise and burning rate should be augmented by unstable flame formation, the flame instabilities must be considered in the explosion pressure evaluation.     

The effect of orifice plates with different shapes on explosion propagation of premixed methane–air in a semi-confined pipeline

The effect of internal shape of obstacles on the deflagration of premixed methane–air (concentration of 10%) was experimentally investigated in a semi-confined steel pipeline (with a square cross section size of 80 mm × 80 mm and 4 m long). The obstacles used in this study were circular, square, triangular and gear-shaped (4-teeth, 6-teeth and 8-teeth) orifice plates with a blockage ratio of 75%, and the perimeter of the orifice was regarded as a criterion for determining the sharpness of the orifice plate. The overpressure history, flame intensity histories, flame front propagation speed, maximum flame intensity and peak explosion overpressure were analyzed. The explosion in the pipeline can be divided into two stages: initial explosion and secondary explosion. The secondary explosion is caused by recoiled flame. The perimeter is positively related to the intensity of the recoiled flame and the ability of orifice plate to suppress the explosion propagation. In addition, the increase in the perimeter will cause the acceleration of the flame passing through the orifice plate, while after the perimeter of the orifice reaches a certain value, the effect of the increase in perimeter on explosion excitation becomes no obvious. The overpressure (static pressure) downstream of the orifice plate is the result of the combined effect of explosion intensity and turbulence. The increase in perimeter leads to the increase in turbulence downstream of the orifice plate which in turn causes more explosion pressure to be converted into dynamic pressure.     

Spray and explosion characteristics of methanol and methanol-benzene blends near azeotrope formation: Effects of temperature,concentration, and benzene content

The explosion hazard of flammable liquids leaking to form spray in storage and transportation at ambient temperature has not been systematically investigated. This work presents new results from experimental investigations of the atomization and explosion characteristics of methanol, and methanol-benzene blends forming near the azeotrope under different initial conditions (initial temperature (298.15–318.15 K), methanol concentration (198–514.8 g/m³) and benzene content (41–81%)) in a 20-L spherical vessel. The empirical formulas for Sauter Mean Diameter (SMD) of the droplets and the maximum explosion pressure with respect to the initial temperature and methanol concentration were obtained from the quantitative analysis. Compared to the explosion hazard of pure methanol and methanol-benzene blends spray, the results showed that the maximum rate of pressure rise and maximum explosion temperature of methanol-benzene blends were relatively low. Furthermore, the effect of carbon soot formation on the explosion hazard during explosion development was analyzed.     

初始温度和压力对排污空间甲烷-空气混合物爆燃特性影响的模拟研究

市政排污空间作为城市公共基础设施的重要组成部分，易积聚可燃气体形成爆炸性环境。结合排污空间的特殊环境条件，采用Fluidyn-MP多物理场数值模拟软件，建立了20 L球形爆炸罐分析模型，通过改变初始温度和初始压力，对排污空间甲烷-空气混合物爆燃特性及其变化规律进行模拟研究。结果表明:初始温度升高导致甲烷-空气混合物最大爆炸压力降低，缩短了到达最大爆炸压力的时间；初始压力增加导致最大爆炸压力急剧升高，并延长了到达最大爆炸压力的时间；最大爆炸压力对初始压力的敏感程度远大于初始温度的影响。此外，随着初始温度和初始压力的升高，爆炸火焰平均传播速度增加，而火焰传播速度对初始温度较敏感。     

Observations of microscopic characteristics of post-explosion coal dust samples

To reveal the microscopic characteristics of the post-explosion coal dust samples, coal dust explosion tests were performed in a 20 L spherical vessel. The explosion characteristic parameters, such as the maximum pressure (P_max), the maximum rate of pressure rise ((dP/dt)_max), ignition time (t) and the deflagration index (K_St) were recorded. Meanwhile, the post-explosion dust samples were collected and analyzed. The research efforts include particle size distribution analysis, SEM analysis and FTIR analysis of dust samples before and after the explosion. The particle size range of post-explosion dust samples became wider according to the mass percent analysis. The microscopic appearance of samples in same particle size range showed some similarity. The porous structure of dust samples was observed by improving the SEM magnification. The chemical structure of dust samples before and after explosion was analyzed by FTIR.     

长径比对管道油气爆炸特性与火焰传播规律影响研究*

为了探究长径比对油气爆炸传播特性与火焰传播规律的影响,为复杂管道受限空间油气爆炸防控提供理论参考,结合油气爆炸与爆炸抑制工程实际需要,构建不同长径比管道油气爆炸模拟实验系统,在此基础上开展不同初始浓度的预混油气-空气混合气爆炸实验。研究结果表明:管道内部的预混油气爆炸超压信号呈先上升后下降的趋势,由于耗散以及憋压效应导致超压下降平稳后仍大于初始压力;同时长径比增加会导致达到最大爆炸超压的油气浓度增加,油气爆炸超压峰值随着长径比的增加呈现上升→下降→上升的规律,小长径比管道的油气爆炸超压峰值高于大长径比管道,但同为小长径比管道或大长径比管道工况的实验结果对比显示爆炸超压峰值随着长径比增加而提升;而超压上升速率则会随着长径比的增加而上升;长径比的增加同时也会促进火焰的加速传播并减小火焰持续时间。     

不同形状受限空间内油气爆燃特性的实验研究

基于实验对4个不同形状的20L容器内的油气爆燃过程进行了研究,探讨了不同形状受限空间内爆炸压力荷载的变化和火焰行为的区别。结果表明:管道（短管和长管）的压力时序曲线较容积式受限空间（球形容器和立方体容器）的压力时序曲线更复杂,并且出现压力振荡;随着初始浓度的增加,超压值和平均升压速率均先增大后减小,在浓度为1.74%时达到最大值,此时,超压从大到小依次为:长管>短管>立方体>球形容器,平均升压速率从大到小依次为:短管>立方体>长管>球形容器;在爆燃初期,立方体中火焰行为为半球状层流火焰→扁平层流火焰,火焰速度先增大后减小,最大速度为12.5 m/s,长管中火焰行为为半球状层流火焰→拉伸指状火焰,火焰速度一直增大,最大速度为40 m/s。     

球形压力容器中甲烷-氢气-空气爆炸过程数值模拟及实验研究

为研究受限空间内甲烷-氢气-空气混合气体爆炸特性参数分布规律,在20 L球形压力容器装置内开展甲烷-氢气-空气混合气体爆炸实验,探究掺氢比变化对当量比为1的甲烷-氢气-空气混合气体爆炸过程的影响;运用Fluent数值模拟软件,采用标准k-ε湍流模型,结合层流有限速率燃烧模型,探究混合气体爆炸过程中燃烧特性(爆炸温度、压力、密度等)与反应时间的变化规律。研究结果表明：爆炸过程中,添加一定氢气时爆炸压力峰值、爆炸压力上升速率峰值增大,而到达峰值时间缩短;反应初期,中心点火处密度下降,反应釜各处密度持续上升;距离点火点越远,密度变化越大,反应釜中压力分布基本相同。研究结果可为甲烷-氢气-空气混合燃料的安全使用提供相关参考。