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THERMAL AND ELECTROLYTIC DECOMPOSITION AND IGNITION OF HAN-WATER SOLUTIONS

机译:水溶液的热和电解分解与点火

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Thermal and electrolytic decomposition and ignition of water solutions of hydroxylammonium nitrate (HAN, [NH3OH](+)[NO3](-)) are investigated. Experiments are conducted to demonstrate the feasibility of electrolytic ignition for HAN-based ionic liquid propellants. As a consequence of electrolysis, the propellant decomposes to NH2OH, HNO3, HONO, HNO, N2O, N-2, NO, NO2, H2O, H-2(g), and O-2(g). These species then initiate a series of gas phase reactions, governed by the H-O-N kinetics scheme, and lead to ignition. Electrochemical mechanisms are established and incorporated into an existing chemical kinetics scheme for thermal decomposition of HAN-water solutions. The analysis treats the liquid and gas phases separately, and matches their respective processes at the interfacial boundary to determine the overall decomposition and ignition characteristics. Results are benchmarked against experimental data for the species evolution in the condensed phase, as well as laser-induced ignition delay of 13 M HAN-water solution. The effects of electric current (0-2.5 A), propellant volume (0.1-0.3 cc), initial temperature (300-450 K), and HAN concentration (9-13 M) on the ignition behaviors are investigated systematically. The ignition delay decreases with increasing electric current as a power-law function: tau(ign) = AI(-n), where A = 3.95 and n = 0.95 for a 0.1 cc 13 M HAN-water solution at an initial condition of 300 K and 1 atm. The exponent n and coefficient A are decreasing functions of the initial temperature. For a given power, decreasing the initial volume of HAN-water solution increases the current density available for electrolysis, and expedites the ignition process. The work represents the first theoretical study of its kind on this topic.
机译:研究了硝酸羟铵(HAN,[NH3OH](+)[NO3](-))水溶液的热和电解分解及着火情况。进行实验以证明对基于HAN的离子液体推进剂进行电解点火的可行性。电解的结果是,推进剂分解为NH2OH,HNO3,HONO,HNO,N2O,N-2,NO,NO2,H2O,H-2(g)和O-2(g)。然后这些物种根据H-O-N动力学方案引发一系列气相反应,并导致着火。建立了电化学机制,并将其纳入现有的用于HAN水溶液热分解的化学动力学方案中。该分析分别处理液相和气相,并在界面边界处匹配它们各自的过程,以确定整体分解和着火特性。将结果与凝结相中物种演化的实验数据以及13 M HAN水溶液的激光诱导点火延迟进行对比。系统地研究了电流(0-2.5 A),推进剂体积(0.1-0.3 cc),初始温度(300-450 K)和HAN浓度(9-13 M)对点火行为的影响。点火延迟随着电流的幂律函数的增加而减小:tau(ign)= AI(-n),其中对于初始温度为300的0.1 cc 13 M HAN水溶液,A = 3.95和n = 0.95 K和1个大气压。指数n和系数A是初始温度的递减函数。对于给定的功率,减少HAN水溶液的初始体积会增加可用于电解的电流密度,并加快点火过程。该作品代表了该主题的首次此类理论研究。

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