Continuous (hydro-)dechlorination of aromatic chloride compounds in benzyltoluene

Benzyltoluene is an attractive liquid organic hydrogen carrier (LOHC) compound but needs to be purified after its technical synthesis to remove chloride impurities that would harm the Pt-based hydrogenation and dehydrogenation catalysts used for the reversible LOHC loading and unloading with hydrogen. For this purpose the dechlorination of chlorobenzyltoluene in a benzyltoluene matrix was studied in a continuously operated trickle bed reactor using a commercially available nickel catalyst. The results indicate that the removal of chlorobenzyltoluene is mainly adsorption based. Rapid aging experiments with purposely added chloroaromatic compounds (chlorobenzene and chloronaphthalene) in quantities of up to 9000 ppm suggest that high chloroaromatic loadings lead to reduced dechlorination activity due to a rapid blocking of active sites. The dechlorination capacity per gram of the used catalyst material was determined to be in the range of 2 kg of technical benzyltoluene. • Technical grade H0-BT needs removal of chloride impurities before usage as LOHC. • Chlorobenzyltoluene was dechlorinated using nickel in a trickle bed reactor. • The dechlorination process is primarily adsorption-based on the nickel-catalyst. • Chloroaromatic impurities block active sites, lowering dechlorination activity. • A dechlorination capacity of 2 kg H0-BT per gram of nickel-catalyst was estimated.

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Publication Details

Journal
International Journal of Hydrogen Energy
Published
2025-04-18
DOI
https://doi.org/10.1016/j.ijhydene.2025.04.116
Citations
3
Primary Topic
Environmental remediation with nanomaterials
Type
article
Field-Weighted Citation Impact
2.02
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article

Continuous (hydro-)dechlorination of aromatic chloride compounds in benzyltoluene

Patrick Schühle, Kerstin Mitländer, Peter Wasserscheid, Michael Geißelbrecht et al.
3 citations
International Journal of Hydrogen Energy
Environmental remediation with nanomaterials
2.02
article

Continuous (hydro-)dechlorination of aromatic chloride compounds in benzyltoluene

Patrick Schühle, Kerstin Mitländer, Peter Wasserscheid, Michael Geißelbrecht, Phillip Nathrath, J. Henseler, F. Rullo
article en
3 citations

Abstract

Benzyltoluene is an attractive liquid organic hydrogen carrier (LOHC) compound but needs to be purified after its technical synthesis to remove chloride impurities that would harm the Pt-based hydrogenation and dehydrogenation catalysts used for the reversible LOHC loading and unloading with hydrogen. For this purpose the dechlorination of chlorobenzyltoluene in a benzyltoluene matrix was studied in a continuously operated trickle bed reactor using a commercially available nickel catalyst. The results indicate that the removal of chlorobenzyltoluene is mainly adsorption based. Rapid aging experiments with purposely added chloroaromatic compounds (chlorobenzene and chloronaphthalene) in quantities of up to 9000 ppm suggest that high chloroaromatic loadings lead to reduced dechlorination activity due to a rapid blocking of active sites. The dechlorination capacity per gram of the used catalyst material was determined to be in the range of 2 kg of technical benzyltoluene. • Technical grade H0-BT needs removal of chloride impurities before usage as LOHC. • Chlorobenzyltoluene was dechlorinated using nickel in a trickle bed reactor. • The dechlorination process is primarily adsorption-based on the nickel-catalyst. • Chloroaromatic impurities block active sites, lowering dechlorination activity. • A dechlorination capacity of 2 kg H0-BT per gram of nickel-catalyst was estimated.

International Journal of Hydrogen EnergyVol. 128
Forschungszentrum Jülich (DE), Friedrich-Alexander-Universität Erlangen-Nürnberg (DE), Helmholtz Institute Erlangen-Nürnberg (DE)
Openalex Percentile: Top 14%
Environmental remediation with nanomaterials
2.02
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Continuous (hydro-)dechlorination of aromatic chloride compounds in benzyltoluene — Patrick Schühle, Kerstin Mitländer, et al. · International Journal of Hydrogen Energy (2025) | TGRS Research Map | TGRS