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Millifluidics for Chemical Synthesis and Time-resolved Mechanistic Studies
Published on: November 27, 2013
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Submicrosecond Aggregation during Detonation Synthesis of Nanodiamond
Joshua A Hammons1, Michael H Nielsen1, Michael Bagge-Hansen1
1Lawrence Livermore National Laboratory, 7000 East Avenue, Livermore, California 94550 United States.
The Journal of Physical Chemistry Letters
|June 1, 2021
Summary
Detonation nanodiamond (DND) aggregates rapidly after formation, within microseconds, impacting their properties. Understanding this aggregation is key to controlling DND characteristics.
Area of Science:
- Materials Science
- Nanotechnology
- Chemical Physics
Background:
- Detonation nanodiamonds (DND) tend to form aggregates, diminishing their nanoscale properties and necessitating post-processing.
- The kinetics and mechanisms of DND aggregation remain experimentally uncharacterized, hindering strategies for aggregation control.
Purpose of the Study:
- To experimentally determine the time scales and mechanisms of detonation nanodiamond aggregation.
- To provide insights into controlling DND properties by understanding early-stage aggregation.
Main Methods:
- Time-resolved small-angle X-ray scattering (TR-SAXS) was employed.
- SAXS measurements were conducted in situ during high-explosive detonations producing carbon nanomaterials.
Main Results:
- DND aggregation into low fractal dimension structures was observed as early as 0.1 microseconds post-detonation.
- A distinct scattering signal, indicative of graphitic products, was observed concurrently.
- Explosives producing nano-onions showed no hierarchical scattering within 10 microseconds, suggesting delayed aggregation.
Conclusions:
- DND aggregation occurs on very short timescales, comparable to particle formation during detonation.
- The findings highlight the rapid nature of DND aggregation and its dependence on the carbon phase formed.
- This research provides a foundation for developing methods to mitigate DND aggregation.

