TY - JOUR
T1 - Olefin-Assisted Electrochemical Recycling of Homogeneous Hydrosilylation Catalysts in Nonpolar Media
AU - Jeon, Jemin
AU - Chung, Ching Hsiu
AU - Roh, Shisang
AU - Bergman, Evan
AU - Wang, Miao
AU - Su, Xiao
N1 - The Dow Chemical Company is acknowledged for financial support of this work through the University Partnership Initiative. X.S. and J.J. thank Dr. Megan Donaldson, Dr. Dan Hickman, and Dr. Reza Panah at the Dow Chemical Company for a helpful discussion on the recycling system development. J.J. would like to thank Dr. Johannes Elbert for synthesizing PVF and Prof. Catherine J. Murphy for the DLS instrumentation. The authors acknowledge the use of the instrumentation at NMR Lab in the School of Chemical Sciences (SCS) at University of Illinois Urbana-Champaign.
PY - 2025/3/24
Y1 - 2025/3/24
N2 - Homogeneous platinum catalysts for hydrosilylation are essential for the chemical industry and society, through the production of commodities such as functional silicones. However, the high boiling points of the products and the low concentration of the homogeneous catalysts make the implementation of traditional separation methods difficult. Catalyst loss becomes a core sustainability and techno-economic challenge. In addition, the highly active platinum-based catalysts for hydrosilylation have remarkable susceptibility to deactivation upon reaction completion. Recently, redox-mediated electrosorption has been successfully demonstrated in a number of electrically conductive media as a separation platform. However, industrial hydrosilylation systems are carried out in highly nonconductive media. Therefore, developing an electrochemical recycling system in realistic, nonconductive hydrosilylation media can be transformative for sustainable homogeneous catalysis and chemical manufacturing. Here, we overcome these challenges for hydrosilylation catalyst recycling by introducing a strongly coordinating vinyl ligand and enabling the recycling of these Pt catalysts in solvent-free, nonpolar reactant media through two distinct loops for catalyst recycling and electrosorbent regeneration. The coordinating olefin ligand maintains catalytic activity after the reaction and prevents particle aggregation, a primary mechanism for deactivation. The Pt catalyst stabilized by the coordinated ligand can be reversibly adsorbed and released by the electrosorbent, demonstrating 100% catalytic activity retention and over 90% Pt release efficiency. A techno-economic analysis supports the economic potential of the electrochemical recycling system, with cost savings of >5k USD/kgPt. By combining chemical design and electrochemical engineering, we demonstrate the sustainable electrochemical recycling of industrially relevant hydrosilylation catalysts in practical nonconductive media.
AB - Homogeneous platinum catalysts for hydrosilylation are essential for the chemical industry and society, through the production of commodities such as functional silicones. However, the high boiling points of the products and the low concentration of the homogeneous catalysts make the implementation of traditional separation methods difficult. Catalyst loss becomes a core sustainability and techno-economic challenge. In addition, the highly active platinum-based catalysts for hydrosilylation have remarkable susceptibility to deactivation upon reaction completion. Recently, redox-mediated electrosorption has been successfully demonstrated in a number of electrically conductive media as a separation platform. However, industrial hydrosilylation systems are carried out in highly nonconductive media. Therefore, developing an electrochemical recycling system in realistic, nonconductive hydrosilylation media can be transformative for sustainable homogeneous catalysis and chemical manufacturing. Here, we overcome these challenges for hydrosilylation catalyst recycling by introducing a strongly coordinating vinyl ligand and enabling the recycling of these Pt catalysts in solvent-free, nonpolar reactant media through two distinct loops for catalyst recycling and electrosorbent regeneration. The coordinating olefin ligand maintains catalytic activity after the reaction and prevents particle aggregation, a primary mechanism for deactivation. The Pt catalyst stabilized by the coordinated ligand can be reversibly adsorbed and released by the electrosorbent, demonstrating 100% catalytic activity retention and over 90% Pt release efficiency. A techno-economic analysis supports the economic potential of the electrochemical recycling system, with cost savings of >5k USD/kgPt. By combining chemical design and electrochemical engineering, we demonstrate the sustainable electrochemical recycling of industrially relevant hydrosilylation catalysts in practical nonconductive media.
KW - adsorptive separation
KW - electrochemical separation
KW - homogeneous catalyst recycling
KW - hydrosilylation
KW - redox-responsive material
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U2 - 10.1021/jacsau.4c01071
DO - 10.1021/jacsau.4c01071
M3 - Article
C2 - 40151264
AN - SCOPUS:105001071679
SN - 2691-3704
VL - 5
SP - 1221
EP - 1231
JO - JACS Au
JF - JACS Au
IS - 3
ER -