Abstract
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.
| Original language | English |
|---|---|
| Pages (from-to) | 9816-9821 |
| Number of pages | 6 |
| Journal | New Journal of Chemistry |
| Volume | 49 |
| Issue number | 23 |
| DOIs | |
| State | Published - 20 May 2025 |
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