TY - JOUR
T1 - Highly Efficient Preparation of Graphite Oxide without Water Enhanced Oxidation
AU - Yuan, Hong
AU - Ye, Jianglin
AU - Ye, Chuanren
AU - Yin, Songsen
AU - Li, Jieyun
AU - Su, Kai
AU - Fang, Gang
AU - Wu, Yanhong
AU - Zheng, Yaxuan
AU - Ge, Ming
AU - Tang, Runli
AU - Feng, Guanping
AU - Qu, Yan
AU - Zhu, Yanwu
N1 - Publisher Copyright:
©
PY - 2021/3/9
Y1 - 2021/3/9
N2 - Graphite oxide has become an important precursor for graphene oxide, reduced graphene oxide, and a wide range of other graphene-based materials or composites. In numerous Hummers' methods for the preparation of graphite oxide, water is added to promote the oxidization reaction but causes problems of tedious purification and liquid waste, which raises concerns of environment processing cost in the large-scale production of graphite oxide. Herein, we propose a highly efficient oxidization of chemical expandable graphite (CEG) for one-step preparation of graphite oxide while water is not added during the oxidization. This method features a direct separation of the solid reactant from the liquid oxidant, allowing the reuse of waste acid and quick centrifugal washing of products close to neutral pH. This strategy also benefits the highly efficient utilization of the oxidant potassium permanganate (KMnO4), indicated by the high monolayer/bilayer yield (?90%) of graphene oxide for a KMnO4/CEG mass ratio as low as 2.5. Without the hydration reaction, which generally leads to etching of graphitic sheets, the graphene oxide platelets made from this strategy readily maintain a large size of 30?110 μm for the CEG of 80 mesh grids (?175 μm), making the current method suitable for the preparation of thermally and electrically conductive graphene films. This work provides a more efficient and environmentally friendly preparation technique for the industrial production of graphite oxide and relevant materials.
AB - Graphite oxide has become an important precursor for graphene oxide, reduced graphene oxide, and a wide range of other graphene-based materials or composites. In numerous Hummers' methods for the preparation of graphite oxide, water is added to promote the oxidization reaction but causes problems of tedious purification and liquid waste, which raises concerns of environment processing cost in the large-scale production of graphite oxide. Herein, we propose a highly efficient oxidization of chemical expandable graphite (CEG) for one-step preparation of graphite oxide while water is not added during the oxidization. This method features a direct separation of the solid reactant from the liquid oxidant, allowing the reuse of waste acid and quick centrifugal washing of products close to neutral pH. This strategy also benefits the highly efficient utilization of the oxidant potassium permanganate (KMnO4), indicated by the high monolayer/bilayer yield (?90%) of graphene oxide for a KMnO4/CEG mass ratio as low as 2.5. Without the hydration reaction, which generally leads to etching of graphitic sheets, the graphene oxide platelets made from this strategy readily maintain a large size of 30?110 μm for the CEG of 80 mesh grids (?175 μm), making the current method suitable for the preparation of thermally and electrically conductive graphene films. This work provides a more efficient and environmentally friendly preparation technique for the industrial production of graphite oxide and relevant materials.
UR - https://www.scopus.com/pages/publications/85102129872
U2 - 10.1021/acs.chemmater.0c04505
DO - 10.1021/acs.chemmater.0c04505
M3 - Article
AN - SCOPUS:85102129872
SN - 0897-4756
VL - 33
SP - 1731
EP - 1739
JO - Chemistry of Materials
JF - Chemistry of Materials
IS - 5
ER -