Related Experiment Video
Updated: Mar 8, 2026

09:50
Preparation and Reactivity of Gasless Nanostructured Energetic Materials
Published on: April 2, 2015
10.7K
Reactive Ni/Al Nanocomposites: Structural Characteristics and Activation Energy
Christopher E Shuck1, Alexander S Mukasyan1,2
1Department of Chemical and Biomolecular Engineering, University of Notre Dame , Notre Dame, Indiana 46556, United States.
The Journal of Physical Chemistry. A
|January 19, 2017
Summary
Mechanical processing controls reaction kinetics in nickel/aluminum reactive nanocomposites (RNCs). Milling time influences nanostructure and effective activation energy, enabling tunable energetic material performance.
Area of Science:
- Materials Science
- Nanotechnology
- Chemical Engineering
Background:
- Reactive nanocomposites (RNCs) are advanced energetic materials.
- Controlling their nanostructure is key to tuning reaction kinetics.
Purpose of the Study:
- To investigate the relationship between nanostructure and reaction kinetics in Ni/Al RNCs.
- To demonstrate control over reaction kinetics via mechanical processing.
Main Methods:
- Preparation of Ni/Al RNCs using high-energy ball milling for varied durations.
- Quantitative analysis of internal nanostructures using serial focused ion beam sectioning and 3D reconstruction.
- Analysis of reaction kinetics via the electrothermal explosion technique.
Main Results:
- Milling time directly influenced the internal nanostructure and surface area contact of Ni/Al RNCs.
- Effective activation energy (Eef) ranged from 79 to 137 kJ/mol.
- A direct correlation was observed between reactant surface area contact and Eef.
Conclusions:
- Mechanical processing, specifically ball milling, offers precise control over the reaction kinetics of Ni/Al RNCs.
- The nanostructure achieved through milling dictates the energetic performance.
- Understanding the mechanistic effects of activation energies allows for tailored material design.
More Related Videos
Related Concept Videos
meta-Directing Deactivators: –NO2, –CN, –CHO, –⁠CO2R, –COR, –CO2H
7.0K
All meta-directing substituents are deactivating groups. These substituents withdraw electrons from the aromatic ring, making the ring less reactive toward electrophilic substitution. For example, the nitration of nitrobenzene is 100,000 times slower than that of benzene because of the deactivating effect of the nitro group. The first step in an electrophilic aromatic substitution is the addition of an electrophile to form a resonance-stabilized carbocation. The energy diagrams for...
7.0K
Alkali Aggregate Reaction in Concrete
671
The alkali-aggregate reaction in concrete involves natural siliceous minerals in aggregates reacting with alkaline hydroxides derived from cement alkalis. This reaction forms an alkali-silica gel that absorbs water, swells, and increases in volume, which is confined by the surrounding cement paste, creating internal pressures that crack and disrupt the concrete. The extent of expansion and damage can be partly attributed to the alkali-silica reaction's osmotic hydraulic pressure and the...
671
Bond Dissociation Energy and Activation Energy
11.6K
Bond energy is the energy required to break a bond homolytically. These values are usually expressed in units of kcal/mol or kJ/mol and are referred to as bond dissociation energies when given for specific bonds or average bond energies when indicated for a given type of bond over many compounds. Firstly, the bond dissociation energy for a single bond is weaker than that of a double bond, which in turn is weaker than that of a triple bond. Secondly, hydrogen forms relatively strong bonds with...
11.6K

