Pre‐Activation as a Route for Tuning the Kinetics of Mechanochemical Transformations
Abstract
Abstract Learning to control reaction kinetics is essential for translating any chemical technology into real‐world application. Based on time‐resolved in situ powder X‐ray diffraction data, we demonstrate the opportunity to tune mechanochemical reaction rates through the pre‐activation of the starting reagents. For three model co‐crystal systems, the pre‐activation of the most stable reagent yields up to a ca 10‐fold increase in the reaction rate, whilst negligible kinetic enhancement is seen when the less stable reagent is pre‐activated. Moreover, we demonstrate how the polymorphic outcome of mechano‐co‐crystallization is also sensitive to pre‐activation of the starting material. Our results suggest that reproducibility of mechanochemical processes requires detailed understanding over the origin and history of reagent powders, whilst providing a new conceptual framework to design and control mechanochemical reactions.
Article Details
Authors (8)
Christian Heinekamp
Federal Institute for Materials Research and Testing (BAM) Richard‐Willstätter Str 11 Berlin 12489 Germany
Tahlia M. Palmer
School of Chemistry University of Birmingham Birmingham B15 2TT United Kingdom
Dominik Al‐Sabbagh
Federal Institute for Materials Research and Testing (BAM) Richard‐Willstätter Str 11 Berlin 12489 Germany
Anastasia May
Federal Institute for Materials Research and Testing (BAM) Richard‐Willstätter Str 11 Berlin 12489 Germany
Carsten Prinz
Stefan Michalik
Diamond Light Source Ltd, Harwell Science and Innovation Campus
Adam A. L. Michalchuk
Federal Institute for Materials Research and Testing (BAM) Richard‐Willstätter Str 11 Berlin 12489 Germany
Franziska Emmerling
Department of Materials Chemistry, Federal Institute for Materials Research and Testing, Richard-Willstätter-Str. 11, 12489 Berlin, Germany