Related Experiment Video
Updated: Aug 18, 2026

Biomass Conversion to Produce Hydrocarbon Liquid Fuel Via Hot-vapor Filtered Fast Pyrolysis and Catalytic Hydrotreating
Published on: December 25, 2016
One-Step Thermochemical Conversion of Biomass Waste into Superhydrophobic Carbon Material by Catalytic Pyrolysis
De-Chang Li1, Wan-Fei Xu1, Hui-Yuan Cheng1
1CAS Key Laboratory of Urban Pollutants Conversion Department of Applied Chemistry University of Science and Technology of China Hefei 230026 China.
Abstract:
Preparation of superhydrophobic carbon materials from lignocellulosic biomass waste via one-step carbonization is very difficult due to the existences of polar functional groups and ashes, which are extremely hydrophilic. Herein, superhydrophobic carbon materials can be facilely synthesized by catalytic pyrolysis of biomass waste using FeCl3 as catalyst. The results show that the surface energy of lignin-derived char (CharL) is significantly reduced to 19.25 mN m-1 from 73.29 mN m-1, and the water contact angle increased from 0 to 151.5°, by interaction with FeCl3. Multiple characterizations and control experiments demonstrate that FeCl3 can catalyze the pyrolytic volatiles to form a rough graphite and diamond-like carbon layer that isolates the polar functional groups and ashes on CharL, contributing to the superhydrophobicity of the CharL. The one-step catalytic pyrolysis is able to convert different natural biomass waste (e.g., lignin, cellulose, sawdust, rice husk, maize straw, and pomelo peel) into superhydrophobic carbon materials. This study contributes new information related to the interfacial chemistry during the sustainable utilization of biomass waste.
Related Concept Videos
Alkynes to Aldehydes and Ketones: Hydroboration-Oxidation
One of the convenient methods for the preparation of aldehydes and ketones is via hydration of alkynes. Hydroboration-oxidation of alkynes is an indirect hydration reaction in which an alkyne is treated with borane followed by oxidation with alkaline peroxide to form an enol that rapidly converts into an aldehyde or a ketone. Terminal alkynes form aldehydes, whereas internal alkynes give ketones as the final product.
Bioplastics

