Abstract
Probing short-lived reaction species is challenging owing to the need for both high signal-to-noise ratio, which can require long measurement time, and fast time resolution. Here, a novel in situ sample environment is presented that decouples time resolution from measurement time by distributing reaction time over space for the reaction under flow. In the mixing-flow reactor, precursor solutions are mixed at a specific position along the flow path, where the reaction is initiated. As the reaction mixture flows within a reaction capillary, the reaction time increases with distance from the mixing point. A measurement can be taken at a specific distance from the mixing point for as long as is needed to accumulate good statistics without compromising the time resolution of the measurement. Applications of the mixing-flow reactor for pair distribution function measurements of the initial nuclei formed during the hydrolysis of Al3+ at high pH are shown.
| Original language | English |
|---|---|
| Pages (from-to) | 258-264 |
| Number of pages | 7 |
| Journal | Journal of Applied Crystallography |
| Volume | 55 |
| DOIs | |
| State | Published - Apr 1 2022 |
Keywords
- flow reactors
- in situ pair distribution function analysis
- solution X-ray scattering
- time-resolved measurement
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