Numerical investigation on the effects of reaction orders on the flame propagation dynamic behaviors for premixed gas in a closed tube

In this paper, the premixed flame propagation in a closed tube is surveyed using Computational Fluid Dynamics. The propagation characteristics of premixed flame are obtained coupling a single-step reaction mechanism with a laminar flame model. Three single-step reaction mechanisms are established with different reaction orders for hydrocarbon fuels. This study is to establish a wider range of reaction mechanisms and represent actual experimental conditions better. The numerical simulation results demonstrate that reaction orders can affect the tulip flame development. As the flame spreads, the tulip flame fronts become wrinkled. When the reaction order is 2, there are more wrinkles in the flame front and the degree of wrinkles is more obvious. Reaction orders also affect the flame tip velocity and the flame skirt velocity. The main reason is that laminar flame speeds are significantly different. When the reaction orders are 1.5 and 2, laminar flame speeds are mainly affected by temperature, which respectively increase by about 25% and 75%. When the reaction order is 1, the pressure is crucial for the variation of laminar flame speed. The laminar flame speed decreases by about 33%.     

Experimental study on the effect of diluent gas on H2/CO/air mixture turbulent premixed flame

To study the effects of different diluents on the propagation characteristics of H₂/CO/air mixture turbulent premixed flames, a series of experiments were carried out in a turbulent premixed flame experimental system. The effects of turbulence intensity (0.49–1.31 m/s), dilution gas content (10%, 20%, and 30%), hydrogen fraction (50%, 70%, and 90%), and equivalence ratio (0.6, 0.8, and 1.0) on the turbulent premixed flame were studied. The results show that with the increase in hydrogen fraction or turbulence intensity or equivalence ratio, the S_T and u_t increase at the same radius. Compared with N₂ dilution, CO₂ dilution showed a more obvious inhibition effect on S_T. With the increase of Ka, S_T;35mm/u’ gradually decreased, and the extent of S_T;35mm/u’ decrease gradually became smaller. As the intensity of turbulence increases or the hydrogen fraction increases, the slope of S_T,35mm/u’ with Da/Le gradually decreases. In the turbulence intensity range of this experiment, the u_t,35mm/μ_l under nitrogen dilution condition has a larger floating range. The growth rate of u_t,35mm/μ_l at a low equivalence ratio is significantly higher than that at a high equivalence ratio.     

Flame characteristics of premixed H2-air mixtures explosion venting in a spherical container through a duct

The explosion venting duct can effectively reduce the hazard degree of a gas explosion and conduct the venting energy to the safe area. To investigate the flame quantitative propagation law of explosion venting with a duct, the effects of hydrogen fraction and explosion venting duct length on jet flame propagation characteristics of premixed H₂-air mixtures were analyzed through experiment and simulation. The experiment results under initial conditions of room temperature and 1 atm show that when hydrogen fraction was high enough, part of the unburned hydrogen was mixed with air again to reach an ignitable concentration, resulting in the secondary combustion was easier produced and the duration of the secondary flame increased. With the increase of venting duct length, the flame front distance and propagation velocity increased. Meanwhile, the spatial distribution of pressure field and temperature field, and the propagation process and mechanism of the flame venting with a duct were analyzed using FLUENT software. The variation of the pressure wave and the pressure reflection oscillation law in the explosion venting duct was captured. Therefore, in the industrial explosion venting design with a duct, the hazard caused by the coupling of venting pressure and venting flame under different fractions should be considered comprehensively.     

基于柠檬酸-铕纳米配位聚合物构建荧光探针快速检测汤煲中5’-肌苷酸含量

基于柠檬酸-铕金属有机纳米配体聚合物（citrate/europium lanthanide coordination polymer nanoparticles，Cit/Eu LCP NPs）构建快速检测肉品汤煲中5’-肌苷酸（inosine-5’-monophosphate，5’-IMP）的荧光探针。研究结果表明，5’-IMP对Cit/Eu?LCP?NPs有良好的荧光猝灭作用。在最佳条件下，该荧光探针在5’-IMP?2.5～200?μg/mL的质量浓度范围内呈现出良好的线性关系，检出限为0.17?μg/mL，且具备良好的抗干扰、稳定性和重复性。为了验证方法可行性，将该方法应用于实际鸡汤样品中的5’-IMP检测，测得加标回收率为97.85%～103.95%，可为快速检测肉品汤煲中5’-IMP提供新的思路和方法。     

Surface sedimentation and adherence of Nano‐SiO2 to improve thermal stability and flame resistance of melamine‐formaldehyde foam via sol‐gel method

Melamine‐formaldehyde foam possesses intrinsic flame retardance; however, relative poor thermal stability and a certain amount of heat release rate restrict its applications in heated environment to a degree. In the present research, sol‐gel method has been adopted to precipitate nano‐SiO₂ particles on the surface of the melamine‐formaldehyde foam's fibers to construct a protective inorganic gel layer. Taking advantages of the shielding effects of the gel layer, the thermal‐oxygen degradation of the foam can be greatly retarded during heating; hence, the thermal stability is remarkably improved, and the flame retardance is further enhanced. In addition, introducing a small amount of membrane‐forming agent in the sol‐gel system can make the depositional nano‐SiO₂ particles well adhered to avoid dusting.     

Thermal analysis of polymer ignition

Gas phase criteria for the onset of flaming combustion of solids in fires are used to locate a critical temperature T_cr in a nonisothermal analysis (TA) experiment that corresponds to the surface temperature of the solid at ignition in a fire test, T_ign. This critical TA temperature occurs at low conversion of solid to gaseous fuel so it is independent of the heating rate in the test or the thermal decomposition reaction model. However, T_cr depends on the thermal properties of the polymer and the conditions of the fire test in which the gas phase criteria were measured. Nonisothermal analysis data in nitrogen and air were obtained for 20 polymers by thermogravimetric analysis and microscale combustion calorimetry. The critical temperatures T_crs obtained from TA experiments compared favorably with analytic results for a simple polymer ignition model and finite element simulations and were in qualitative agreement with ignition temperatures measured in standardized fire tests.     

A methodology for predicting and comparing the full‐scale fire performance of similar materials based on small‐scale testing

Reconstructive fire testing is an important tool used by fire investigators to determine the cause, origin, and progression of a particular fire. Accurate reconstruction of the fire requires the laboratory structure to be outfitted with materials that, in terms of contribution to fire growth, perform similarly to the original materials found at the fire scene. Therefore, a procedure was developed to enable fire investigators to select these replacement materials on the basis of a quantitative assessment of their relative fire performance. This procedure consists of gram‐scale and/or milligram‐scale standard testing accompanied by inverse numerical modeling of these tests, which is used to obtain relevant material properties. A numerical model composed of a detailed pyrolysis submodel and empirical flame heat feedback submodels, which were developed in this study, is subsequently employed to simulate the early stages of the Room Corner Test, which was selected to represent full‐scale material performance. The results of these simulations demonstrate that this procedure can successfully differentiate between fire growth propensities of several commercially available medium density fiberboards.     

Core–shell type multi‐arm azide polymers based on hyperbranched copolyether as potential energetic materials in solid propellants

A series of novel multi‐arm azide copolymers (POGs) with the same hyperbranched poly[3‐ethyl‐3‐(hydroxymethyl)oxetane] core (PEHO‐c) and different content of linear glycidyl azide polymer shell (GAP‐s) have been synthesized by sequential cationic ring‐opening polymerization and azidation. Detailed structural information of these copolyethers was deduced from Fourier transform infrared, ¹H NMR and inverse gated decoupled ¹³C NMR spectroscopies, matrix‐assisted laser desorption ionization time‐of‐flight mass spectrometry, gel permeation chromatography and elemental analysis. The molecular weight of POG having GAP‐s and PEHO‐c with a molar ratio 14.95:1 (R_s/c) was around 31 000 g mol^?1, far above that of linear GAP (around 4000 g mol^?1). The apparent viscosity and glass transition temperature (?51 to ?23 °C) decreased first and then slightly increased with increasing molecular weight. Thermal analysis revealed that all the obtained POGs exhibited excellent resistance to thermal decomposition up to 220 °C. Moreover, the energetic properties, investigated using oxygen bomb calorimetric measurements, indicated that the enthalpy of formation of the POGs was higher than that of general linear GAP, but similar to that of branched GAP under reasonable R_s/c. The compatibilities of the POGs with common materials used in solid propellants were studied using differential scanning calorimetry and the results indicated that the POGs had good compatibility with these materials. © 2017 Society of Chemical Industry     

Synergistic flame retardant effects of activated carbon and molybdenum oxide in poly(vinyl chloride)

The synergistic effects of activated carbon (AC) and molybdenum oxide (MoO₃) in improving the flame retardancy of poly(vinyl chloride) (PVC) were investigated. The effects of AC, MoO₃ and their mixture with a mass ratio of 1:1 on the flame retardancy and smoke suppression properties of PVC were studied using the limiting oxygen index and cone calorimeter tests. It was found that the flame retardancy of the relatively cheaper AC was slightly weaker than that of MoO₃. In addition, the incorporation of AC and MoO₃ greatly reduced the total heat release and improved smoke suppressant property of PVC composites. When the total content of AC and MoO₃ was 10 phr, PVC/AC/MoO₃ had the lowest peak heat release rate and peak smoke production rate values of 173.80 kW m^?2 and 0.1472 m² s^?1, which represented reductions of 47.3 and 59.9%, respectively, compared with those of PVC. Furthermore, thermogravimetric analysis and gel content tests were used to analyze the flame retardant mechanism of AC and MoO₃, with results showing that AC could promote early crosslinking in PVC. Char residue left after heating at 500 °C was analyzed using scanning electron microscopy and Raman spectroscopy, and the results showed that MoO₃ produced the most compact char, with the smallest and most organized carbonaceous microstructures. © 2017 Society of Chemical Industry