We proposed with excitement a novel molecular co-assembly (MCSA) that can effectively overcome the agglomeration of energetic materials. Through the coordinated self-assembly of polymethyl methacrylate-polyvinyl acetate (PMMA-PVA) with honeycomb-like structure and nanoparticles, a controlled and orderly distribution of nitroamine explosive (cyclotetramethylenetetranitramine, HMX; cyclotrimethylenetrinitramine, RDX; and hexanitrohexaazaisowurtzitane, CL-20) structure was achieved, above all, resolving the agglomeration problem availably. The modification ability of PMMA to RDX, HMX, and CL-20 at different temperatures was simulated by Materials Studio, which provided guidance for the ambient temperature of collaborative self-assembly. In order to compare the priority of the morphology and performance, RDX/PMMA-PVA, HMX/PMMA-PVA, and CL-20/PMMA-PVA composite particles with the same PMMA content were also fabricated by water suspension coating method, respectively. Structural characterizations and thermal stability of the composites were systematically studied by scanning electron microscopy (SEM), X-ray diffraction (XRD), fourier-transform infrared (FT-IR) spectra, and differential scanning calorimeter (DSC). Moreover, the safety performance was analyzed by qualitative testing of impact sensitivity and friction sensitivity. The solid spherical PBX prepared via collaborative self-assembly all exhibited a perfect spherical structure, smooth, and flat coating, without any agglomeration. They had the same crystalline structure as the uncoated explosives, simultaneously demonstrating lower impact sensitivity and higher energy performance. The application of collaborative self-assembly technology has broken through the key technical bottleneck of the shell material being easy to form a separate phase in the desensitization coating of explosives, availably resolved the problems of particle exposure and low coverage during the coating, thus possessing vital significance for reference in the design and fabrication of PBXs with core-shell structure.

By observing the microdroplet microstructure before and after demulsification, it is found that the Fe₃N@F magnetic demulsifier exhibits favorable coalescence, flocculation, and bridging capabilities.

The crystal morphology of high energetic materials plays a crucial role in aspects of their safety performance such as impact sensitivity. In order to reveal the crystal morphology of ammonium dinitramide/pyrazine-1,4-dioxide (ADN/PDO) cocrystal at different temperatures, the modified attachment energy model (MAE) was used at 298, 303, 308, and 313 K to predict the morphology of the ADN/PDO cocrystal under vacuum and ethanol. The results showed that under vacuum conditions, five growth planes of the ADN/PDO cocrystal were given, which were (1 0 0), (0 1 1), (1 1 0), (1 1 −1), and (2 0 −2). Among them, the ratios of the (1 0 0) and (0 1 1) planes were 40.744% and 26.208%, respectively. In the (0 1 1) crystal plane, the value of S was 1.513. The (0 1 1) crystal plane was more conducive to the adsorption of ethanol molecules. The order of binding energy between the ADN/PDO cocrystal and ethanol solvent was (0 1 1) > (1 1 −1) > (2 0 −2) > (1 1 0) > (1 0 0). The radial distribution function analysis revealed that there were hydrogen bonds between the ethanol and the ADN cations, van der Waals interactions with the ADN anions. As the temperature increased, the aspect ratio of the ADN/PDO cocrystal was reduced, making the crystal more spherical, which helped to further reduce the sensitivity of this explosive.

This paper aims to address the issue of environmental pollution resulting from marine oil spills by evaluating the oil adsorption performance of commonly used fence materials. Conventional oil adsorption materials exhibit limited rates and capacities for oil adsorption. Existing methods have proven insufficient in meeting the requirements for efficient and rapid oil–water separation. A new oil-absorbing barrier was developed by utilizing high oil adsorption resin as the primary material and hydroxypropyl methyl cellulose (HPMC) as the binder, leveraging the exceptional oil adsorption and hydrophobic properties of P(BMA-SMA-St)/MIL-101(Fe) resin. The oil-absorbing fence was characterized using scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR) and thermogravimetric analysis (TGA). The oil adsorption rates of carbon tetrachloride, toluene, diesel and gasoline by the oil adsorption fence with 25 g/L resin content were 101.26 g/m², 68.12 g/m², 35.19 g/m², and 46.69 g/m², respectively. After 120 h of UV irradiation, the coating’s oil absorption capacity remained nearly unchanged, and it demonstrated outstanding mechanical, chemical, and wear resistance. As a result, the oil adsorption fence possesses the capability to rapidly absorb oil from the water’s surface during the process of containing oil pollution, leading to positive social and economic impacts.

In this study, a new type of highly efficient and recyclable magnetic-fluorine-containing polyether composite demulsifier (Fe₃O₄@G-F) was synthesized by the solvothermal method to solve the demulsification problem of oil–water emulsion. Fe₃O₄@G-F was successfully prepared by grafting fluorinated polyether onto Fe₃O₄ and graphene-oxide composites. Fe₃O₄@G-F was characterized using scanning electron microscopy (SEM), Fourier-transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM), and X-ray photoelectron spectroscopy (XPS). Taking the self-made crude-oil emulsion as the experimental object, the demulsification mechanism of the demulsifier and the influence of external factors, such as the temperature and pH value, on the demulsification performance of the demulsifier are discussed. The results show that the demulsification efficiency of the Fe₃O₄@G-F emulsion can reach 91.38% within 30 min at a demulsifier dosage of 750 mg/L, pH of 6, and a demulsification temperature of 60 °C. In neutral and acidic environments, the demulsification rate of the demulsifier is more than 90%. In addition, Fe₃O₄@G-F has been proven to have good magnetic effects. Under the action of an external magnetic field, Fe₃O₄@G-F can be recycled and reused in a two-phase system four times, and the demulsification efficiency is higher than 70%. This magnetic nanoparticle demulsifier has broad application prospects for various industrial and environmental processes in an energy-saving manner.

To tackle the challenges of non-recyclability and environmental hazards posed by conventional polyamine demulsifiers, this research has adopted reed sourced from oil fields as the primary material. Specifically, by leveraging an in-situ pyrolysis-co-precipitation approach, we synthesized magnetic biochar (MBC) and grafted polyamine molecules using KH-570, developing a composite demulsifier (MPRB) with interfacial activity and magnetic responsiveness. Material characterization indicated that MBC features a hierarchical porous structure characterized by a specific surface area of 372 m ² ∙g ^-1 . Moreover, it also contains ultra-high magnetic Fe ₃ O ₄ nanocrystals, which boast a saturation magnetization of 39.87 emu∙g ^-1 . As a result, this configuration enhances the magnetic response rate by 40% relative to conventional carriers. Post-functional modification, MPRB, capitalizing on the synergistic effect of mesoporous confinement and the amphiphilic nature of polyamine groups, significantly reduced the interfacial tension of emulsions from 42.29 mN∙m ^-1 to 26.02 mN∙m ^-1 . Additionally, it adjusted the surface wettability to achieve an amphiphilic balanced state, evidenced by a water contact angle of 87.3°. Demulsification experiments revealed that MPRB-3, when subjected to conditions of 70°C and 400 mg∙L ^-1 , displayed time-dependent demulsification efficiency for high-viscosity crude oil emulsions and diesel emulsions. After 60 min, the demulsification rates were 85.23% and 96.23%, respectively, which increased to 90.72% and 98.28% after 120 min. Following rapid separation facilitated by an external magnetic field within 25 s, the demulsification rates sustained at 85.82% and 93.82% even after six cycles of reuse. This durability is attributed to the high retention rate of the Fe ₃ O ₄ magnetic core and the minimal structural degradation of the biochar framework. Through the synergistic enhancement of interfacial activity and the integration of magnetic separation technology, this study achieves a green, full-process chain for demulsifiers, including efficient demulsification, rapid recovery, and recyclable regeneration, offering an eco-friendly solution for oil field produced liquids management and aligning with sustainability.