Brandon J. Wallace, Musarrat Makhnun, Rana Bachnak, Pyeongeun Kim, Musahid Ahmed, Cari S. Dutcher, Kevin Roger Wilson, Ashok Ajoy
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引用次数: 0
Abstract
Chemical reactions in microscale compartments, such as aerosols and emulsions, can exhibit significantly faster reaction rates relative to macroscale containers. This enhancement in chemistry is often due to the elevated importance of surfaces as reaction vessels are reduced to picoliter volumes. While most studies have focused on the air-water interface of droplets, there are comparably fewer studies of reactions in micron-scale aqueous solutions encapsulated by oil. Here we investigate the condensation reaction of pyruvic acid (PA) to form zymonic acid (ZA) and water. Using microfluidics and optical trapping, chemical kinetics are measured in monodisperse micron-sized emulsions in-situ via Raman spectroscopy. Relative to a macroscopic bulk solution, which exhibits little to no reaction over many days, we find efficient production of ZA over the same time period. A kinetic model is developed to elucidate the role of the interface in accelerating the microdroplet reaction kinetics. After quantifying the surface partitioning of PA from interfacial tension measurements, the rate coefficient for the condensation reaction at the oil-water interface is determined to be 1.8 x 10-2 M-1 s-1. This rate coefficient is estimated to be 105 larger than the reaction rate in bulk aqueous solutions. Compared to previous studies of accelerated ZA formation at the air-water interface on nanodroplets, we find that the reaction at the oil-water interface is 20 times more efficient. Despite this difference, the overall ZA formation rate in emulsions is significantly slower than in the same-sized aerosols, which arises from the weaker partitioning of PA to the oil-aqueous relative to air-water interface. These results highlight the interplay between interfacial partitioning and reactivity in accelerating chemistry in microcompartments and provides new insights into how interfacial composition influences condensation reactions.
在微尺度的容器中,如气溶胶和乳剂中的化学反应,相对于大尺度的容器,可以表现出明显更快的反应速率。化学上的这种增强通常是由于当反应容器体积减小到皮升时,表面的重要性提高了。虽然大多数研究都集中在液滴的空气-水界面上,但对油封装的微米尺度水溶液中的反应的研究相对较少。本文研究了丙酮酸(PA)的缩合反应生成酶酸(ZA)和水。利用微流体和光学捕获技术,通过拉曼光谱原位测量了单分散微米级乳剂的化学动力学。相对于宏观体溶液,在许多天内几乎没有反应,我们发现在相同的时间内ZA的有效生产。建立了一个动力学模型来解释界面在加速微滴反应动力学中的作用。从界面张力测量中量化PA的表面分配后,确定了油水界面冷凝反应的速率系数为1.8 x 10-2 M-1 s-1。这个速率系数估计比散装水溶液中的反应速率大105。与以往的研究相比,我们发现纳米液滴在空气-水界面加速ZA形成的反应效率提高了20倍。尽管存在这种差异,但乳液中ZA的总体形成速度明显慢于相同大小的气溶胶,这是由于相对于空气-水界面,PA在油-水界面的分配较弱。这些结果强调了界面分配和反应性之间的相互作用在加速微室化学反应中,并为界面组成如何影响缩合反应提供了新的见解。
期刊介绍:
Chemical Science is a journal that encompasses various disciplines within the chemical sciences. Its scope includes publishing ground-breaking research with significant implications for its respective field, as well as appealing to a wider audience in related areas. To be considered for publication, articles must showcase innovative and original advances in their field of study and be presented in a manner that is understandable to scientists from diverse backgrounds. However, the journal generally does not publish highly specialized research.