多相混合反应微流控装置的设计与制造

M. W. Losey, R. J. Jackman, S. Firebaugh, M. Schmidt, K. Jensen
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引用次数: 216

摘要

利用硅微加工技术,构建了用于多相催化反应的微化学器件。设计背后的动机,制造方法,和实验表征提出了两类设备。第一种设计包括多个平行通道和集成过滤结构,以结合标准催化材料。这些催化剂以多孔颗粒的形式在填充床上排列。第二种装置以覆盖微结构通道的薄层形式加入多孔硅作为催化剂载体。这些微结构的通道模拟了填料床的结构,相对于开放的通道增强了传质。在几十微米尺度上结合特征的能力可以通过促进多相的混合和分散来减少传质限制。将催化剂支撑结构直接集成到微反应器的通道中,可以精确定义床层特性,包括支撑的大小、形状和排列,以及空隙率。这种设计将广泛适用于增强传感、化学和生化转换装置的传输和活性表面积。使用多孔硅作为载体的集成催化剂进行环己烯气-液-固加氢反应的反应速率优于填充床方法所获得的反应速率。在这两种情况下,传质系数至少比传统实验室反应器好100倍。
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Design and fabrication of microfluidic devices for multiphase mixing and reaction
Using silicon microfabrication technology, microchemical devices have been constructed for the purpose of conducting heterogeneously catalyzed multiphase reactions. The motivation behind the design, the fabrication approach, and the experimental characterization are presented for two classes of devices. The first design involves multiple parallel channels with integrated filter structures to incorporate standard catalytic materials. These catalysts are in the form of finely divided porous particles in a packed-bed arrangement. The second device involves the incorporation of porous silicon as a catalyst support, in the form of a thin layer covering microstructured channels. These microstructured channels simulate the structure of a packed bed and enhance mass transfer relative to an open channel. The ability to incorporate features at the tens-of-microns scale can reduce the mass-transfer limitations by promoting mixing and dispersion for the multiple phases. Directly integrating the catalyst support structures into the channels of the microreactor allows the precise definition of the bed properties, including the support's size, shape and arrangement, and the void fraction. Such a design would find broad applicability in enhancing the transport and active surface area for sensing, chemical, and biochemical conversion devices. Reaction rates for the gas-liquid-solid hydrogenation of cyclohexene using the integrated catalyst with porous silicon as a support compare favorably to those rates obtained with the packed-bed approach. In both cases, the mass transfer coefficient is at least 100 times better than conventional laboratory reactors.
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