TY - JOUR
T1 - Ferrocene-functionalized room-temperature ionic liquids as green bipropellant hypergolic fuels
AU - Fang, Haichao
AU - Fan, Mingren
AU - Song, Siwei
AU - Wang, Yi
AU - Zhang, Qinghua
N1 - Publisher Copyright:
© 2025 The Royal Society of Chemistry.
PY - 2025/5/20
Y1 - 2025/5/20
N2 - It is well-established that numerous metallic compounds accelerate hydrogen peroxide (H2O2) decomposition, significantly decreasing the ignition delay (ID) time of hydrocarbon fuels. However, such catalysts, particularly ferrocene derivatives, are typically solid-state materials, rendering them incompatible with liquid-liquid bipropellant systems where ID correlates critically with additive solubility. To address this limitation, we synthesized a novel class of ferrocene-based room-temperature ionic liquids (ILs) through systematic modulation of alkyl chain lengths on the ferrocenium cation paired with anion volume optimization. These tailored ILs exhibited hypergolic ignition upon contact with 90% H2O2. Furthermore, blending the synthesized ILs with 1-amino-4-methylpiperazine (PIP) markedly decreased ID. Notably, the compound [FcCH2N(CH3)2CH2CH 00000000 00000000 00000000 00000000 11111111 00000000 11111111 00000000 00000000 00000000 CH2]+[IM-BH2CN]− (F6) achieved the most pronounced ID reduction, with its ID decreasing from 358 ms to 115 ms.
AB - It is well-established that numerous metallic compounds accelerate hydrogen peroxide (H2O2) decomposition, significantly decreasing the ignition delay (ID) time of hydrocarbon fuels. However, such catalysts, particularly ferrocene derivatives, are typically solid-state materials, rendering them incompatible with liquid-liquid bipropellant systems where ID correlates critically with additive solubility. To address this limitation, we synthesized a novel class of ferrocene-based room-temperature ionic liquids (ILs) through systematic modulation of alkyl chain lengths on the ferrocenium cation paired with anion volume optimization. These tailored ILs exhibited hypergolic ignition upon contact with 90% H2O2. Furthermore, blending the synthesized ILs with 1-amino-4-methylpiperazine (PIP) markedly decreased ID. Notably, the compound [FcCH2N(CH3)2CH2CH 00000000 00000000 00000000 00000000 11111111 00000000 11111111 00000000 00000000 00000000 CH2]+[IM-BH2CN]− (F6) achieved the most pronounced ID reduction, with its ID decreasing from 358 ms to 115 ms.
UR - http://www.scopus.com/inward/record.url?scp=105006557655&partnerID=8YFLogxK
U2 - 10.1039/d5nj01606a
DO - 10.1039/d5nj01606a
M3 - 文章
AN - SCOPUS:105006557655
SN - 1144-0546
VL - 49
SP - 9816
EP - 9821
JO - New Journal of Chemistry
JF - New Journal of Chemistry
IS - 23
ER -