Related Experiment Video
Updated: May 6, 2026

Development, Characterization, and Evaluation of CAGE-based Ionic Liquid Systems for Transdermal Delivery
Published on: September 26, 2025
Two Promising Ionic Energetic Cocrystals Based on ADN and AP
Yunshu Zhao1, Yibo Zhou1, Xiaoyan Zhang1
1School of Materials and Chemistry, Southwest University of Science and Technology, Mianyang 621010, Sichuan, People's Republic of China.
Abstract:
Ammonium dinitramide (ADN) and ammonium perchlorate (AP) are two representative mainstream oxidizers. However, their practical applications in advanced energetic formulations are severely limited by multiple factors, such as high hygroscopicity and insufficient thermal stability for ADN, relatively low energy density for AP, and unfavorable enthalpy of formation for both. To address these drawbacks, this work introduces 4-amino-1,2,4-triazole (4-ATA), a coformer with a high enthalpy of formation, to prepare two ionic energetic cocrystals with excellent comprehensive properties: ADN/4-ATA (cocrystal 1) and AP/4-ATA (cocrystal 2). Compared with their respective raw oxidizers, cocrystal 1 exhibits higher thermal stability (Td > 200 °C) and lower impact sensitivity (2-kg drop hammer, H50 = 51.5 cm), whereas cocrystal 2 shows significantly improved detonation performance, with its detonation velocity (VD) and detonation pressure (P) increased by 12.6 and 23.7%, respectively. Therefore, the preparation of ionic cocrystals offers an effective approach to enhancing the overall performance of ionic oxidizers.
Related Concept Videos
Ion Exchange
Ionic Bonds
When atoms gain or lose electrons to achieve a more stable electron configuration they form ions. Ionic bonds are electrostatic attractions between ions with opposite charges. Ionic compounds are rigid and brittle when solid and may dissociate into their constituent ions in water. Covalent compounds, by contrast, remain intact unless a chemical reaction breaks them.
Opposing Charges Hold Ions Together in Ionic Compounds
Ionic bonds are reversible electrostatic interactions between ions...
Adrenergic Agonists: Chemistry and Structure-Activity Relationship
Aromatic ring substitutions: Substituting the aromatic ring with –OH groups at positions 3 and 4 yields catecholamines (e.g., epinephrine), which have a high affinity for adrenoceptors. Hydrogen bonding between –OH groups and receptors enhances adrenergic activity.
Separation of...
Ionic Crystal Structures
Most monatomic ions behave as charged spheres, and their attraction for ions of opposite charge is the same in every direction. Consequently, stable structures for ionic compounds result (1) when ions of one charge are surrounded by as many ions as possible of the opposite...
Anionic Chain-Growth Polymerization: Overview
Ionic Association

