This mini-review focuses on two different miniaturizing approaches: the first one describes the generation and use of droplets flowing within a millifluidic tool as individual batch microreactors. The second one reports the use of high pressure microflows in chemistry. Millifluidics is an inexpensive, versatile and easy to use approach which is upscaled from microfluidics. It enables one to produce hierarchically organized multiple emulsions or particles with a good control over sizes and shapes, as well as to provide a convenient data acquisition platform dedicated to slow or rather fast chemical reactions, i.e., from hours to a few minutes. High-pressure resistant devices were recently fabricated and used to generate stable droplets from pressurized fluids such as supercritical fluid-liquid systems. We believe that supercritical microfluidics is a promising tool to develop sustainable processes in chemistry.
High-pressure vapor−liquid equilibrium data were measured for two binary systems: carbon dioxide +
dimethyl sulfoxide at four temperatures from 309 to 329 K and pressures up to 13 MPa, and carbon
dioxide + dichloromethane at 311.41 K and 326.95 K and pressures up to 9.5 MPa. Bubble points were
determined by a synthetic method where a mixture of known composition is prepared in a sapphire cell
of variable volume. The reliability of the equipment and method was established through comparison
with literature on the carbon dioxide + ethanol system. These measurements were made at 314.45 and
324.17 K.
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