TY - JOUR
T1 - HTPFA-Coated AlB2 with Enhanced Combustion Performance as a High-Energy Fuel
AU - Wang, Jiangfeng
AU - Zhao, Wanjun
AU - Shen, Chen
AU - Ou, Yapeng
AU - Jiao, Qingjie
N1 - Publisher Copyright:
© 2025 by the authors.
PY - 2025/4
Y1 - 2025/4
N2 - High-energy boron-based fuel aluminum-diboride (AlB2) has attracted much attention in the field of solid propellants. However, the low reactivity of AlB2 hindered its further application. In this study, highly reactive AlB2@hydroxyl-terminated perfluoropolyether alcohol (AlB2@HTPFA) composites with a core–shell structure were prepared by coating AlB2 with functionalized fluoropolymers by using a facile one-step in situ polymerization method. AlB2@HTPFA composites with varying polymer contents (0, 5, 10, and 15 wt%) were obtained. The in situ polymerization strategy enables precise control over the polymer coating thickness and interfacial interactions, which is critical for optimizing the reactivity and thermal stability of composites. The morphology and structure were characterized, and the microcore–shell structure of AlB2@HTPFA was obtained. Compared with raw AlB2, the combustion efficiency of coated fuel increased by 4.1%, 5.6%, and 7.5%, respectively, with varying polymer contents. Meanwhile, the reactivity of AlB2@HTPFA (5 wt%) was 0.65 MPa/s, which is ~1.5 times that of AlB2. Additionally, the ignition and combustion characteristics of AlB2@HTPFA were investigated by laser ignition experiments with potassium perchlorate (KP) as an oxidant. The results revealed that AlB2@HTPFA/KP composites showed a greatly reduced combustion duration compared to uncoated AlB2. The ignition and combustion enhancement mechanism of AlB2@HTPFA was proposed. During the ignition process, the existence of HTPFA can result in a pre-ignition reaction, thus raising its reaction activity. This work provided a promising candidate for high-energy fuel that can be used in energetic materials.
AB - High-energy boron-based fuel aluminum-diboride (AlB2) has attracted much attention in the field of solid propellants. However, the low reactivity of AlB2 hindered its further application. In this study, highly reactive AlB2@hydroxyl-terminated perfluoropolyether alcohol (AlB2@HTPFA) composites with a core–shell structure were prepared by coating AlB2 with functionalized fluoropolymers by using a facile one-step in situ polymerization method. AlB2@HTPFA composites with varying polymer contents (0, 5, 10, and 15 wt%) were obtained. The in situ polymerization strategy enables precise control over the polymer coating thickness and interfacial interactions, which is critical for optimizing the reactivity and thermal stability of composites. The morphology and structure were characterized, and the microcore–shell structure of AlB2@HTPFA was obtained. Compared with raw AlB2, the combustion efficiency of coated fuel increased by 4.1%, 5.6%, and 7.5%, respectively, with varying polymer contents. Meanwhile, the reactivity of AlB2@HTPFA (5 wt%) was 0.65 MPa/s, which is ~1.5 times that of AlB2. Additionally, the ignition and combustion characteristics of AlB2@HTPFA were investigated by laser ignition experiments with potassium perchlorate (KP) as an oxidant. The results revealed that AlB2@HTPFA/KP composites showed a greatly reduced combustion duration compared to uncoated AlB2. The ignition and combustion enhancement mechanism of AlB2@HTPFA was proposed. During the ignition process, the existence of HTPFA can result in a pre-ignition reaction, thus raising its reaction activity. This work provided a promising candidate for high-energy fuel that can be used in energetic materials.
KW - AlB
KW - combustion characteristic
KW - functionalized fluoropolymer
KW - ignition
KW - preignition reaction
UR - https://www.scopus.com/pages/publications/105002331186
U2 - 10.3390/ma18071452
DO - 10.3390/ma18071452
M3 - Article
AN - SCOPUS:105002331186
SN - 1996-1944
VL - 18
JO - Materials
JF - Materials
IS - 7
M1 - 1452
ER -