Skip to content
naulon
Not checkedNot checked for notices yet.

Recent Advances in Photocatalytic Transformation of Carbohydrates Into Valuable Platform Chemicals

Huan Chen, Kun Wan, Fangjuan Zheng and 5 more

Frontiers in Chemical Engineering · 2021

doi:10.3389/fceng.2021.615309 (opens in a new tab)

We email you when a new notice or a question about this paper appears.

Abstract

In response to the less accessible fossil resources and deteriorating environmental problems, catalytic conversion of the abundant and renewable lignocellulosic biomass to replace fossil resources for the production of value-added chemicals and fuels is of great importance. Depolymerization of carbohydrate and its derivatives can obtain a series of C5-C6 monosaccharides (e.g., glucose and xylose) and their derived platform compounds (e.g., HMF and furfural). Selective transformation of lignocellulose using sustainable solar energy via photocatalysis has attract broad interest from a growing scientific community. The unique photogenerated reactive species (e.g., h+, e−, •OH, •O2−, and 1O2), novel reaction pathways as well as the mild reaction conditions make photocatalysis a “dream reaction.” This review is aimed to provide an overview of the up-to-date contributions achieved in the selective photocatalytic transformation of carbohydrate and its derivatives. Photocatalytic methods, properties and merits of different catalytic systems are well summarized. We then put forward future perspective and challenges in this field.

Abstract licence: CC BY

References74

    40 more references, whose wording the paper’s licence keeps private.

    All 74 references

    Reads

    Read by people on this page

    None yet.

    Checked or read by AI through naulon

    None yet.

    A person counts once a day per paper. We keep no cookie and no address: a reader is a hash that changes every day. Any month under five reads shows no number.

    Are you an author?

    Is this your paper?

    Claim it to add your note and be paid when agents cite it. Free.