HiGee Strategy toward Rapid Mass Production of Porous Covalent Organic Polymers with Superior Methane Deliverable Capacity
Weichao Zhang, Yujia Liu, Yong Luo, Chengpeng Xie, Zhonghua Xiang, Jian‐Feng Chen
Abstract
Abstract High porosity with well‐defined molecular reticulation along with strong stability is desired for natural gas delivery. The catalyzed Yamamoto‐type Ullmann cross‐coupling route with efficient terminal halogen removal capability is currently used to prepare porous organic materials with high specific surface area as well as ultrahigh hydrothermal stability. As a typical fast coupling reaction, the traditional stirred solvothermal approach shows the limitation of macroscopic reaction kinetics due to the increasing viscosity of the reaction mixture with the molecular network growth until it turns to a jelly‐like consistency. Herein, a high‐gravity chemical synthetic strategy to achieve rapid and economical preparation of a class of, but not limited to, covalent organic polymers (COPs) with high hydrothermal stability using the Ullman cross‐coupling route is described. The viscous fluid is vigorously split into homogeneous microdroplets through the rotating packed bed (RPB) under the HiGee environment. The HiGee approach shortens the traditional reaction time from 600 to 15 min as well as reduces the usage of high‐cost nickel (0) catalyst by 40 wt%. Specially, the COP‐10 obtained with the HiGee approach displays an excellent deliverable methane capacity of 415 cm 3 STP g −1 at 298 K with working pressures 5–65 bar, which is higher than that of most reported porous organic materials.