Wireless μLED packed beds for scalable continuous multiphasic photochemistry†

IF 3.4 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Esai Daniel Lopez, Patricia Zhang Musacchio and Andrew R. Teixeira
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Abstract

Photochemical and photocatalytic reactions are a powerful emerging tool in the green synthesis of organic molecules. In contrast to thermochemical reactions, they promise greater energy efficiency, milder reaction conditions, and a decrease in the number of synthesis steps. Unfortunately, conventional batch photochemical systems are not inherently scalable, making translation to industrial applications challenging. Fundamentally, this is most clearly attributed to the penetration depth of light, as constrained by the Beer–Lambert relationship: as the size of the reactor is increased, the depth of light penetration into liquid medium decreases exponentially. Small-diameter plug flow reactors with external illumination have recently been employed industrially to 1) transition photochemistry from batch to continuous flow, and 2) overcome light penetration challenges by employing millimeter-scale optical paths; however these often present with substantial pressure drops and scalability challenges. In this work, a fixed bed reactor is packed with wireless μLEDs (μLED-PBR) and engineered to scale the oxidation of α-terpinene using a homogeneous rose-bengal photosensitizer. Utilizing μLEDs as packing allows for internal volumetrically scalable illumination from 250 or 500 μLEDs. Not only is the μLED packing efficient at delivering photons, but it also statically induces turbulence and mixing of the biphasic streams within the reactor. Unlike tubular plug flow reactors, the μLED-PBR design is volumetrically scalable. During operation, a co-current trickle flow regime was established with a 29 μm liquid film flowing over the μLEDs. In stark contrast to those typical in small channel tubular flow reactors, the packed bed experienced negligible hydrodynamic pressure drop penalties. The photochemical space time yield of the reactor normalized to the power consumption for the μLED-PBR was three orders of magnitude greater than other externally illuminated thin film flow reactors for the same chemistry: 1411 mmol W−1 per day compared to 1.34 mmol W−1 per day.

Abstract Image

Abstract Image

用于可扩展连续多相光化学的无线 μLED 填料床
光化学反应和光催化反应是绿色合成有机分子的新兴有力工具。与热化学反应相比,它们具有更高的能效、更温和的反应条件以及更少的合成步骤。遗憾的是,传统的间歇式光化学系统本身不具备可扩展性,因此将其转化为工业应用具有挑战性。从根本上说,最明显的原因在于光的穿透深度,受比尔-朗伯关系的制约:随着反应器尺寸的增大,光穿透液体介质的深度呈指数级下降。带有外部照明的小直径塞流式反应器最近已在工业上得到应用,目的是:1)将光化学从间歇式转变为连续式;2)通过采用毫米级光路克服光穿透的挑战;然而,这些反应器通常会产生巨大的压降,在可扩展性方面存在挑战。在这项研究中,我们在固定床反应器中安装了无线μLED(μLED-PBR),并利用同质玫瑰红光敏剂对α-萜品烯的氧化进行了放大。利用 μLED 作为填料,可以从 250 μLED 或 500 μLED 进行内部体积可扩展的照明。μLED 填料不仅能有效地提供光子,还能在反应器内静态地引起湍流和双相流的混合。与管式塞流反应器不同,μLED-PBR 设计可按体积扩展。在运行过程中,μLED 上流动着 29 μm 的液膜,形成了同流涓流。与小通道管式流反应器中的典型情况截然不同,填料床的流体动力压降几乎可以忽略不计。反应器的光化学时空产率与 μLED-PBR 的耗电量相比,在相同化学成分的情况下,要比其他外部照明薄膜流动反应器高出三个数量级:每天 1411 mmol W-1 而不是每天 1.34 mmol W-1。
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来源期刊
Reaction Chemistry & Engineering
Reaction Chemistry & Engineering Chemistry-Chemistry (miscellaneous)
CiteScore
6.60
自引率
7.70%
发文量
227
期刊介绍: Reaction Chemistry & Engineering is a new journal reporting cutting edge research into all aspects of making molecules for the benefit of fundamental research, applied processes and wider society. From fundamental, molecular-level chemistry to large scale chemical production, Reaction Chemistry & Engineering brings together communities of chemists and chemical engineers working to ensure the crucial role of reaction chemistry in today’s world.
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