TY - JOUR
T1 - Unveiling New Product Formations beyond Conventional Pathways in De-Halogenation of Halo-Acetic Acids Using Ni-Encapsulated Sol-Gel Catalysts †
AU - Vidyadharan, Kavya
AU - Meyerstein, Dan
AU - Marks, Vered
AU - Burg, Ariela
AU - Meistelman, Michael
AU - Albo, Yael
N1 - Publisher Copyright:
© 2024 by the authors.
PY - 2024/9
Y1 - 2024/9
N2 - The urgency of water remediation and the conversion of toxic pollutants into non-toxic compounds is increasingly crucial in our industrialized world. Heterogeneous catalysts based on metal nanoparticles, which are cost-effective, non-toxic, and readily available, have garnered significant attention in the market due to their unique catalytic properties. This study presents sol–gel-based hybrid silica matrices that encapsulate nickel, designed for the efficient reductive de-halogenation of tri-bromoacetic acid (TBAA), di-bromoacetic acid (DBAA), mono-bromoacetic acid (MBAA), tri-chloroacetic acid (TCAA), mono-chloroacetic acid (MCAA), and Chloroacetanilide (CAA). A detailed study of the product distribution from each halo-acetic acid (HAA) is presented. The study points out that other products are formed from Ni-catalyzed reduction reactions of HAAs, breaking the conventional rules of stepwise reduction mechanisms. The plausible mechanisms of the catalytic processes are discussed.
AB - The urgency of water remediation and the conversion of toxic pollutants into non-toxic compounds is increasingly crucial in our industrialized world. Heterogeneous catalysts based on metal nanoparticles, which are cost-effective, non-toxic, and readily available, have garnered significant attention in the market due to their unique catalytic properties. This study presents sol–gel-based hybrid silica matrices that encapsulate nickel, designed for the efficient reductive de-halogenation of tri-bromoacetic acid (TBAA), di-bromoacetic acid (DBAA), mono-bromoacetic acid (MBAA), tri-chloroacetic acid (TCAA), mono-chloroacetic acid (MCAA), and Chloroacetanilide (CAA). A detailed study of the product distribution from each halo-acetic acid (HAA) is presented. The study points out that other products are formed from Ni-catalyzed reduction reactions of HAAs, breaking the conventional rules of stepwise reduction mechanisms. The plausible mechanisms of the catalytic processes are discussed.
KW - catalysis
KW - halo-acetic acids
KW - nickel
KW - reduction
KW - sol-gel
UR - http://www.scopus.com/inward/record.url?scp=85205046254&partnerID=8YFLogxK
U2 - 10.3390/catal14090596
DO - 10.3390/catal14090596
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AN - SCOPUS:85205046254
SN - 2073-4344
VL - 14
JO - Catalysts
JF - Catalysts
IS - 9
M1 - 596
ER -