Solid‐State Investigation, Storage, and Separation of Pyrophoric PH3 and P2H4 with α‐Mg Formate

Author:

Widera Anna1ORCID,Thöny Debora1ORCID,Aebli Marcel1ORCID,Oppenheim Julius Jacob2ORCID,Andrews Justin L.2ORCID,Eiler Frederik1ORCID,Wörle Michael1ORCID,Schönberg Hartmut1,Weferling Norbert3,Dincǎ Mircea2ORCID,Grützmacher Hansjörg1ORCID

Affiliation:

1. Department of Chemistry and Applied Biosciences, ETH Zürich Vladimir-Prelog-Weg 1–5/10 8093 Zürich Switzerland

2. MIT Department of Chemistry Massachusetts Institute of Technology 77 Massachusetts Ave. Cambridge MA-02139 18-393 USA

3. WefConsult GmbH Knapsackstr. 39 50354 Huerth Germany

Abstract

AbstractPhosphane, PH3—a highly pyrophoric and toxic gas—is frequently contaminated with H2 and P2H4, which makes its handling even more dangerous. The inexpensive metal–organic framework (MOF) magnesium formate, α‐[Mg(O2CH)2], can adsorb up to 10 wt % of PH3. The PH3‐loaded MOF, PH3@α‐[Mg(O2CH)2], is a non‐pyrophoric, recoverable material that even allows brief handling in air, thereby minimizing the hazards associated with the handling and transport of phosphane. α‐[Mg(O2CH)2] further plays a critical role in purifying PH3 from H2 and P2H4: at 25 °C, H2 passes through the MOF channels without adsorption, whereas PH3 adsorbs readily and only slowly desorbs under a flow of inert gas (complete desorption time≈6 h). Diphosphane, P2H4, is strongly adsorbed and trapped within the MOF for at least 4 months. P2H4@α‐[Mg(O2CH)2] itself is not pyrophoric and is air‐ and light‐stable at room temperature.

Funder

Deutsche Forschungsgemeinschaft

Eidgenössische Technische Hochschule Zürich

National Science Foundation

Publisher

Wiley

Subject

General Chemistry,Catalysis

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