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Microwave reactor engineering of zeolites synthesis.

机译:微波反应器工程合成沸石。

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Microwave chemistry has expanded over the last two decades due to the enhanced reaction rates achieved for many processes, including organic synthesis, inorganic synthesis and polymerization. Significant time and energy saving can be realized using microwave chemistry, which is important both commercially and for the environment.;One of the most exciting and commercially/technologically significant areas where microwave energy has been demonstrated to influence the kinetics and selectivity is in the synthesis of nanoporous materials, such as zeolites. New nanoporous materials can be created, and the times for their syntheses can be significantly reduced, involving using less energy. By reducing the times by up to over an order of magnitude, continuous production would be possible to replace batch synthesis.;However, the mechanism and engineering for the enhanced rates of these syntheses are unknown. The results from different laboratories are not consistent, and experimental details are sparse. Therefore, more research is required to unlock the mystery behind this "gee-wiz" chemistry. Furthermore, understanding the fundamental processes leading to rate enhancement by microwaves will also enable the optimization of these microwave heated reactions.;In this work, the formation of SAPO-11 (and AlPO-11), silicalite and NaY zeolites under microwave heating was investigated and the influence of various microwave reactor engineering parameters was studied. Microwaves enhanced the SAPO-11 synthesis by two orders of magnitude over the conventional synthesis. Both nucleation and growth steps were enhanced by the presence of microwaves. Fast microwave heating was not solely responsible for this enhancement. This indicates that non-thermal interactions of material with microwaves are present for this synthesis.;Many microwave reactor engineering parameters were identified as possibly influencing the microwave synthesis of SAPO-11 (and AlPO-11). These factors are precursor volume, reaction temperature, reactor size, stirring, applicator type and microwave frequency. Among those, the reaction temperature had the greatest influence on this SAPO-11 (and AlPO-11) synthesis. Increasing the reaction temperature decreased the nucleation time and increased the growth rate. The crystallization growth rate in the microwave synthesis showed higher activation energy (1.5 times) compared to the conventional synthesis. However, the pre-exponential factor increased by 8 orders of magnitude in the microwave synthesis. Nucleation rate also showed an increase in the activation energy (3.6 times) and an increase in the pre-exponential factor (10 orders of magnitude) by using microwave heating. This substantial increase in the pre-exponential factor could be the reason behind this microwave synthesis enhancement.;High temperature, stirred synthesis, large vessel and using multimode field distribution oven found to be the optimum reaction conditions for microwave synthesis of SAPO-11 (and AlPO-11).;Thermal variations within SAPO-11, silicalite and NaY synthesis solutions were measured using a reaction vessel with multiple fiberoptic temperature probes. NaY synthesis solution has the shortest microwave penetration depth among these zeolite synthesis solutions which led to great thermal variations between the region near the wall (high temperature) and the center (low temperature) when placed in a vessel with diameter 20 times larger than its penetration depth. Increasing these thermal variations led to a decrease in the nucleation time and thus enhanced this NaY microwave synthesis.;Microwave power delivery mode (pulsed vs. continuous) effect on the synthesis of the three zeolites mentioned above was investigated. Pulsing the microwave power required less average power to maintain the synthesis reaction temperature compared to continuous delivery mode. No effect of using pulsed compared to continuous microwave power delivery was found on the nucleation time and the crystal growth for these zeolite syntheses. However, pulsed microwave power delivery produced smaller particles in the case of SAPO-11.;The effect of simultaneous cooling effect on the microwave synthesis of SAPO-11 and silicalite was studied. Increasing the amount of power delivered to the SAPO-11 synthesis while maintaining the reaction temperature fixed using the simultaneous cooling, decreased the nucleation time and increased the growth rate. Smaller particles were formed at high power. Silicalite showed no change in the nucleation time, crystal growth and/or the morphology. This indicates that there is no universal pattern among the microwave synthesis of zeolites. What could be an important factor for one synthesis is not necessarily important for another, and is likely dependant on the dielectric properties and the reaction mechanism.;Key words: Zeolite, SAPO-11, silicalite, NaY, microwave synthesis, nucleation, crystal growth, frequency, reactor engineering, overheating, temperature distribution, pulsing power delivery, simultaneous cooling.
机译:由于在包括有机合成,无机合成和聚合在内的许多过程中提高了反应速率,微波化学在过去的二十年中得到了扩展。微波化学可以节省大量的时间和能源,这对商业和环境都非常重要。合成中已证明微波能影响动力学和选择性的最激动人心且商业/技术上最重要的领域之一纳米多孔材料,例如沸石。可以创造出新的纳米多孔材料,并且可以大大减少合成时间,这涉及到使用更少的能量。通过将时间减少多达一个数量级,可以实现连续生产来代替批量合成。但是,提高这些合成速率的机理和工程性尚不清楚。来自不同实验室的结果不一致,并且实验细节很少。因此,需要更多的研究来揭示这种“ gee-wiz”化学背后的奥秘。此外,了解导致微波速率提高的基本过程还将使这些微波加热的反应最优化。在这项工作中,研究了微波加热下SAPO-11(和AlPO-11),硅沸石和NaY沸石的形成。并研究了各种微波反应器工程参数的影响。微波将SAPO-11合成比常规合成提高了两个数量级。微波的存在增强了成核和生长步骤。快速的微波加热并非仅是这种增强的原因。这表明该合成存在材料与微波的非热相互作用。;已确定许多微波反应器工程参数可能影响SAPO-11(和AlPO-11)的微波合成。这些因素是前体体积,反应温度,反应器尺寸,搅拌,施加器类型和微波频率。其中,反应温度对该SAPO-11(和AlPO-11)的合成影响最大。提高反应温度可减少成核时间并提高生长速率。与常规合成相比,微波合成中的结晶生长速率显示出更高的活化能(1.5倍)。但是,微波合成中的前指数因子增加了8个数量级。通过使用微波加热,成核速率还显示出活化能的增加(3.6倍)和前指数因子的增加(10个数量级)。前指数因子的大量增加可能是微波合成增强的原因。高温,搅拌合成,大容器和使用多模场分布烘箱是微波合成SAPO-11的最佳反应条件(和AlPO-11);;使用带有多个光纤温度探头的反应容器测量SAPO-11,硅沸石和NaY合成溶液中的热变化。在这些沸石合成溶液中,NaY合成溶液的微波穿透深度最短,当放置在直径大于穿透深度20倍的容器中时,NaY合成溶液会导致壁附近区域(高温)和中心区域(低温)之间的巨大热变化。深度。增加这些热变化导致成核时间的减少,从而增强了NaY微波的合成。研究了微波功率传输模式(脉冲与连续)对上述三种沸石合成的影响。与连续输送模式相比,脉动微波功率需要较少的平均功率来维持合成反应温度。与连续微波功率输送相比,使用脉冲对这些沸石合成的成核时间和晶体生长没有影响。然而,在SAPO-11的情况下,脉冲微波功率传递产生较小的颗粒。;研究了同时冷却效应对SAPO-11和硅沸石的微波合成的影响。在同时冷却的同时保持反应温度固定的同时,增加传递给SAPO-11合成的功率数量,减少了成核时间并提高了生长速率。高功率形成较小的颗粒。硅钙石的成核时间,晶体生长和/或形态没有变化。这表明在沸石的微波合成中没有通用模式。一个合成的重要因素对另一个合成不一定重要,并且可能取决于介电性质和反应机理。关键词:沸石,SAPO-11,硅沸石,NaY,微波合成,成核,晶体生长,频率,反应堆工程,过热,温度分布,脉冲功率传输,同时冷却。

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