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Financement britannique (192 297 £) : Époxydation d’alcènes volumineux verts à haut rendement à l’aide de H2O2 généré in situ par des bimétaux à base de sur de la titanosilicalite Ukri 01/09/2024 Recherche et innovation du Royaume-Uni, Royaume Uni

Vue d’ensemble

Texte

Époxydation d’alcènes volumineux verts à haut rendement à l’aide de H2O2 généré in situ par des bimétaux à base de sur de la titanosilicalite

Abstract In response to the challenges of environmental deterioration and resource scarcity, the energy and chemical industry is focusing on eco-sustainable catalysis to achieve diversified feedstocks, environmentally friendly processes, and high-value chemicals. These objectives require green utilization of raw materials to produce commodity and speciality chemicals. Epoxides, as crucial high-value organic chemical intermediates, are widely applied in various fields such as medicine, food, automotive, agriculture, and construction. However, long-chain liquid alkene epoxidation processes rely on conventional organic peroxy acids, chlorohydrin, or Halcon methods. These processes suffer from drawbacks such as significant environmental pollution, intricate processing requirements, or the generation of numerous by-products, all of which contradict the principles of green chemistry and atomic economy. Therefore, there is an urgent need to develop green, straightforward, and highly selective epoxidation processes for long-chain liquid alkenes. Herein, we propose a sustainable pathway for the liquid-phase epoxidation of bulky alkenes using in-situ generated H2O2. The process involves Pd-based bimetallic sites for in-situ H2O2 synthesis and Ti sites in titanosilicalites for alkene epoxidation. Constructing Pd-based bimetallic sites on titanosilicalites allows for the effective coupling of H2O2 generation and alkene epoxidation. The structure-performance relationship will be established between catalytic reactivity and well-defined structure by multi-characterizations (e.g., in-situ X-ray absorption and ultraviolet-visible spectroscopy), as well as elucidate the intrinsic mechanism of bifunctional catalysts through advanced multi-technologies (experimental research, DFT calculation, and microkinetic model). These results align with the "Chemicals Strategy for Sustainability" and are expected to fulfil the zero-pollution ambition of the European Commission.
Category Fellowship
Reference EP/Z002400/1
Status Active
Funded period start 01/09/2024
Funded period end 15/09/2026
Funded value £192 297,00
Source https://gtr.ukri.org/projects?ref=EP%2FZ002400%2F1

Participating Organisations

CARDIFF UNIVERSITY

Cette annonce se réfère à une date antérieure et ne reflète pas nécessairement l’état actuel. L’état actuel est présenté à la page suivante : Cardiff University, Cardiff, Royaume Uni.