Alkaline hydrolysis for degrading the emerging munitions contaminant methylnitroguanidine and regenerating graphene nanoplatelets for sustainable adsorption of munition compounds

• Methylnitroguanide (MeNQ) degraded in high-pH solutions via alkaline hydrolysis. • Breakdown products of MeNQ and nitroguanidine (NQ) included ammonium and nitrite. • High-pH solutions removed adsorbed munitions compounds from graphene nanoplatelets. • Graphene nanoplatelets were capable of adsorptive reuse after regeneration. Alkaline hydrolysis has proven to be an effective treatment technique for several emerging and legacy munition compounds (MCs), including 2,4,6-trinitrotoluene (TNT), hexahydro-1,3,5-trinitro-s-triazine (RDX), 2,4-dinitroanisole (DNAN), and nitroguanidine (NQ). Building on this success, this study evaluates its effectiveness in degrading the emerging insensitive MC methylnitroguanidine (MeNQ) in comparison to NQ. Additionally, the feasibility of regenerating graphene nanoplatelets (GnPs) following adsorption of MCs, including MeNQ, NQ, NTO, TNT, DNAN, and RDX, is investigated. This study is among the first to successfully evaluate MeNQ treatment and proposes a novel strategy to regenerate GnPs for further environmental remediation. Regeneration performance in high-pH solutions was compared with processes using a 30:70 solution of acetonitrile:water and reagent water alone to further determine pH- and solvent-based interactions. In high-pH solutions, NTO was desorbed via electrostatic repulsion, while the other MCs degraded, generating breakdown products consistent with both previous studies and current findings. Additionally, the aqueous ammonium produced during degradation may have been removed by GnPs. The organic-aqueous blend enhanced MC removal, with recovery largely correlating with aqueous solubility, though π-π interactions may have hindered desorption. Adsorption following desorption with these techniques resulted in higher capacities compared to systems using reagent water alone, where desorption aligned with adsorption isotherms. Overall, this study provides valuable insights into MeNQ treatment and the reuse of GnPs for sustainable water remediation.

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Publication Details

Journal
Chemical Engineering Journal Advances
Published
2025-04-04
DOI
https://doi.org/10.1016/j.ceja.2025.100743
Citations
1
Primary Topic
Energetic Materials and Combustion
Type
article
Field-Weighted Citation Impact
0.86
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article

Alkaline hydrolysis for degrading the emerging munitions contaminant methylnitroguanidine and regenerating graphene nanoplatelets for sustainable adsorption of munition compounds

Hollie Cook, Florence Sanchez, Chris S. Griggs, Sheila McLeod et al.
1 citations
Chemical Engineering Journal Advances
Energetic Materials and Combustion
0.86
article

Alkaline hydrolysis for degrading the emerging munitions contaminant methylnitroguanidine and regenerating graphene nanoplatelets for sustainable adsorption of munition compounds

Hollie Cook, Florence Sanchez, Chris S. Griggs, Sheila McLeod, Luke Gurtowski, Sarah Grace Zetterholm
article en
1 citations

Abstract

• Methylnitroguanide (MeNQ) degraded in high-pH solutions via alkaline hydrolysis. • Breakdown products of MeNQ and nitroguanidine (NQ) included ammonium and nitrite. • High-pH solutions removed adsorbed munitions compounds from graphene nanoplatelets. • Graphene nanoplatelets were capable of adsorptive reuse after regeneration. Alkaline hydrolysis has proven to be an effective treatment technique for several emerging and legacy munition compounds (MCs), including 2,4,6-trinitrotoluene (TNT), hexahydro-1,3,5-trinitro-s-triazine (RDX), 2,4-dinitroanisole (DNAN), and nitroguanidine (NQ). Building on this success, this study evaluates its effectiveness in degrading the emerging insensitive MC methylnitroguanidine (MeNQ) in comparison to NQ. Additionally, the feasibility of regenerating graphene nanoplatelets (GnPs) following adsorption of MCs, including MeNQ, NQ, NTO, TNT, DNAN, and RDX, is investigated. This study is among the first to successfully evaluate MeNQ treatment and proposes a novel strategy to regenerate GnPs for further environmental remediation. Regeneration performance in high-pH solutions was compared with processes using a 30:70 solution of acetonitrile:water and reagent water alone to further determine pH- and solvent-based interactions. In high-pH solutions, NTO was desorbed via electrostatic repulsion, while the other MCs degraded, generating breakdown products consistent with both previous studies and current findings. Additionally, the aqueous ammonium produced during degradation may have been removed by GnPs. The organic-aqueous blend enhanced MC removal, with recovery largely correlating with aqueous solubility, though π-π interactions may have hindered desorption. Adsorption following desorption with these techniques resulted in higher capacities compared to systems using reagent water alone, where desorption aligned with adsorption isotherms. Overall, this study provides valuable insights into MeNQ treatment and the reuse of GnPs for sustainable water remediation.

Chemical Engineering Journal AdvancesVol. 22
Vanderbilt University (US), U.S. Army Engineer Research and Development Center (US)
Responsible consumption and production, Industry, innovation and infrastructure
Openalex Percentile: Top 33%
Energetic Materials and Combustion
0.86
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