Related Experiment Video
Updated: Aug 12, 2025

Orientational Transition in a Liquid Crystal Triggered by the Thermodynamic Growth of Interfacial Wetting Sheets
Published on: May 15, 2017
Direct visualization of radiation-induced transformations at alkali halide-air interfaces
Shawn L Riechers1, Nikolay G Petrik2, John S Loring2
1Pacific Northwest National Laboratory, Richland, WA, USA. shawn.riechers@pnnl.gov.
This study reveals how X-rays transform mineral surfaces in air. Using advanced atomic force microscopy, researchers observed nanoscale reactions, providing new insights into atmospheric chemistry.
Area of Science:
- Environmental Science
- Materials Science
- Surface Chemistry
Background:
- Radiation-driven reactions at mineral/air interfaces impact atmospheric chemistry.
- Previous experimental limitations hindered a complete understanding of these processes.
Purpose of the Study:
- To investigate the in situ transformation of mineral surfaces under X-ray irradiation.
- To elucidate the nanoscale mechanisms of radiation-driven reactions at mineral/air interfaces.
Main Methods:
- Utilized a custom atomic force microscope with an integrated X-ray source for in situ nanoscale observation.
- Followed the transformation of potassium bromide surfaces to potassium nitrate.
Main Results:
- Observed direct in situ nanoscale transformation of potassium bromide to potassium nitrate.
- Identified radiolysis initiating step edge dissolution, surface evolution, and crystallite nucleation/growth.
- Demonstrated surface diffusion, controlled by adsorbed water, mediates growth rates.
Conclusions:
- Decoupling irradiation and observation provides valuable insights, unlike high-dose techniques.
- The study offers a novel approach to understanding radiation-driven surface reactions in atmospheric conditions.
More Related Videos
Related Concept Videos
Radical Substitution: Hydrogenolysis of Alkyl Halides with Tributyltin Hydride
The bonds formed in this reaction are stronger than the bonds broken, making it energetically favorable. The reaction follows a radical chain mechanism similar to radical halogenation...
Radical Substitution: Halogenation of Alkanes and Alkyl Substituents
In the initiation step of the reaction, the chlorine molecule undergoes homolytic cleavage in the presence of light or heat, forming two highly reactive chlorine radicals. Propagation occurs in two...
Acid Halides to Alcohols: LiAlH4 Reduction
The mechanism proceeds in three steps. First, the nucleophilic hydride ion attacks the carbonyl carbon of the acid halide to form a tetrahedral intermediate. Next, the carbonyl group is re-formed, and the halide ion departs as a leaving group, generating an aldehyde. A second nucleophilic attack by the hydride yields an alkoxide ion, which, upon protonation, gives a primary alcohol as...
Radical Halogenation: Thermodynamics
Electrophilic Addition to Alkynes: Hydrohalogenation
Halogenation of Alkenes
Consider the bromination of cyclopentene. Molecular bromine is polarized in the proximity of the π electrons of cyclopentene. An electrophilic bromine atom adds across the double bond, forming a cyclic bromonium ion intermediate.

