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Hydrothermal and Pyrolytic Conversion of Biomasses into Catalysts for Advanced Oxidation Treatments
Author(s) -
He Xi,
Zheng Ningchao,
Hu Ruiting,
Hu Zhuofeng,
Yu Jimmy C.
Publication year - 2021
Publication title -
advanced functional materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.069
H-Index - 322
eISSN - 1616-3028
pISSN - 1616-301X
DOI - 10.1002/adfm.202006505
Subject(s) - biochar , catalysis , materials science , pyrolytic carbon , carbon fibers , chemical engineering , photocatalysis , pyrolysis , biomass (ecology) , hydrothermal circulation , radical , nanotechnology , organic chemistry , chemistry , composite material , engineering , oceanography , composite number , geology
Biomasses are very important natural products. Transferring biomass into catalysts for the advanced oxidation process (AOP) via heat treatment has attracted extensive attention. This review systematically introduces and summarizes two kinds of innovative biomass‐based catalysts according to the treating temperature. At low temperature ( < 300 ° C), biomasses are converted into hydrothermal carbonation carbon (HTCC) with semiconductive properties for photocatalysis application. At high temperature ( > 300 ° C), by contrast, the products lose their semiconductive nature and become a conductive carbon‐based conductor (biochar). They usually work as AOP catalysts by activating oxidant of O 2 , H 2 O 2 , and peroxysulfate for environmental treatment. This review summarizes and compares HTCC and biochar according to their formation process, structure, catalytic mechanism, and key points for the activity enhancement. The active units in HTCC are the sp 2 ‐hybridized polyfuran unit while those in biochar are the persistent free radicals, nitrogen‐containing unit, or defects. HTCC converts water into OH radicals by using the photoexcited electron/hole pairs induced by solar illumination, while biochar activates oxidants via the active unit on its surface. More importantly, this review summarizes and demonstrates the key points to obtain high‐efficiency HTCC and biochar catalysts. Finally, conclusions are drawn and the future aspects for biomass‐based catalysis are given.