Unraveling theUnusual Chemistry of the Hydrogen-Peroxide-DrivenHypergolic Ignition of a Cyanoborohydride Ionic Liquid as a Next-GenerationGreen Space Propellant

Hypergolic ionic liquids (HILs) have emerged as promising self-igniting green space propellants in combination with an oxidizer, replacing toxic hydrazine family rocket fuels. Despite numerous new HILs being reported in the literature, there is no systematic study addressing the key reaction mechanism of such hypergolic ignition. Here, the first comprehensive molecular level understanding of this ignition reaction is revealed, exploring a 1-ethyl-3-methylimidazolium cyanoborohydride–hydrogen peroxide ([EMIM][CBH]–H<sub>2</sub>O<sub>2</sub>) green bipropellant pair by a novel chirped-pulse droplet-merging technique in a controlled environment. Mechanistically, the anion [CBH]<sup>−</sup> triggers the hypergolic ignition through facile exoergic oxidation of the boron center yielding boron dioxide (BO<sub>2</sub>) in a barrierless termolecular reaction with two molecules of H<sub>2</sub>O<sub>2</sub>, followed by an enhanced reactivity of the cation [EMIM]<sup>+</sup>, as evidenced from the excess yield of carbon dioxide (CO<sub>2</sub>) and evaluated decay rate constants of [EMIM]<sup>+</sup> <i>in situ</i> during the droplet-merging reaction.

Publication Details

Journal
Figshare
Published
2025-02-14
DOI
https://doi.org/10.1021/acs.jpclett.4c03624.s001
Primary Topic
Genetic and Environmental Crop Studies
Type
article
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article

Unraveling theUnusual Chemistry of the Hydrogen-Peroxide-DrivenHypergolic Ignition of a Cyanoborohydride Ionic Liquid as a Next-GenerationGreen Space Propellant

Figshare
Genetic and Environmental Crop Studies
article

Unraveling theUnusual Chemistry of the Hydrogen-Peroxide-DrivenHypergolic Ignition of a Cyanoborohydride Ionic Liquid as a Next-GenerationGreen Space Propellant

article en

Abstract

Hypergolic ionic liquids (HILs) have emerged as promising self-igniting green space propellants in combination with an oxidizer, replacing toxic hydrazine family rocket fuels. Despite numerous new HILs being reported in the literature, there is no systematic study addressing the key reaction mechanism of such hypergolic ignition. Here, the first comprehensive molecular level understanding of this ignition reaction is revealed, exploring a 1-ethyl-3-methylimidazolium cyanoborohydride–hydrogen peroxide ([EMIM][CBH]–H<sub>2</sub>O<sub>2</sub>) green bipropellant pair by a novel chirped-pulse droplet-merging technique in a controlled environment. Mechanistically, the anion [CBH]<sup>−</sup> triggers the hypergolic ignition through facile exoergic oxidation of the boron center yielding boron dioxide (BO<sub>2</sub>) in a barrierless termolecular reaction with two molecules of H<sub>2</sub>O<sub>2</sub>, followed by an enhanced reactivity of the cation [EMIM]<sup>+</sup>, as evidenced from the excess yield of carbon dioxide (CO<sub>2</sub>) and evaluated decay rate constants of [EMIM]<sup>+</sup> <i>in situ</i> during the droplet-merging reaction.

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Genetic and Environmental Crop Studies
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