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Estimation of Time to Maximum Rate (TMR) Using Kinetic Parameters Determined from DSC

机译:使用DSC确定的动力学参数估算最大速率(TMR)所需的时间

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Kinetic parameters of the decomposition of hazardous chemicals can be applied for theestimation of their thermal behavior under any temperature profile. Presented paper describes theapplication of the advanced kinetic approach for the determination of the thermal behavior also underadiabatic conditions occurring e.g. In batch reactors in case of cooling failure.The kinetics of the decomposition of different samples (different manufacturers and batches) of 3-methyl-4-nitrophenol were investigated by conventional DSC in non-isothermal (few heating ratesvarying from 0.25 to 8.0 K/min) and isothermal (range of 200-260°C) modes. The kinetic parametersobtained with AKTS-Thermokinetics Software were applied for calculating reaction rate and progressunder different heating rates and temperatures and verified by comparing simulated and experimentalsignals. After application of the heat balance to compare the amount of heat generated during reactionand its removal from the system, the knowledge of reaction rate at any temperature profiles allowed thedetermination of the temperature increase due to the self-heating in adiabatic and pseudo-adiabaticconditions.Applied advanced kinetic approach allowed simulation the course of the Heat-Wait-Search(HWS) mode of operation of adiabatic calorimeters. The thermal safety diagram depicting dependenceof Time to Maximum Rate (TMR) on the initial temperature was calculated and compared with theresults of HWS experiments carried out in the system with -factor amounting to 3.2. The influence ofthe Φfactor and reaction progress reached at the end of the HWS monitoring on the TMR is discussed.Presented calculations clearly indicate that even very minor reaction progress reduces the TMRad of 24hrs characteristic for a sample with initial reaction progress amounting to zero.Described estimation method can be verified by just one HWS-ARC, or by one correctly chosen ISOARCrun of reasonable duration by knowing in advance the dependence of the TMR on the initialtemperature for any Φfactor. Proposed procedure results in significant shortening of the measuring timecompared to a safety hazard approach based on series of ARC experiments carried out at the beginningof a process safety evaluation.
机译:危险化学品分解的动力学参数可用于 在任何温度曲线下估算其热行为。论文介绍了 先进的动力学方法在热行为测定中的应用 发生绝热条件,例如在分批反应器中,以防冷却失败。 3-的不同样品(不同制造商和批次)的分解动力学 通过常规DSC在非等温(少量加热速率)下研究了4-硝基硝基苯酚 从0.25至8.0 K / min的温度变化)和等温(200-260°C范围)模式。动力学参数 使用AKTS-Thermokinetics软件获得的反应速率和进度进行计算 在不同的加热速率和温度下,并通过比较模拟和实验进行验证 信号。应用热量平衡后,比较反应过程中产生的热量 并将其从系统中移除,在任何温度曲线下的反应速率知识都可以使 绝热和拟绝热中由于自热引起的温度升高的确定 情况。 应用先进的动力学方法可以模拟热等待搜索的过程 (HWS)绝热热量表的操作模式。描述安全性的热安全图 计算了初始温度下的最大速率时间(TMR),并将其与 系统中进行的HWS实验的结果,-因子总计为3.2。的影响 讨论了HWS在TMR监测结束时达到的Φ因子和反应进度。 给出的计算结果清楚地表明,即使反应很小,TMRad也会降低24 初始反应进程为零的样品的hrs特性。 可以通过一种HWS-ARC或一种正确选择的ISOARC来验证所描述的估算方法 通过提前了解TMR对初始值的依赖来进行合理持续时间的运行 任何Φ因子的温度。拟议的程序大大缩短了测量时间 与基于开始时进行的一系列ARC实验的安全隐患方法相比 过程安全性评估的内容。

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