In the past decade, porous boron nitride (BN) has proven promising as a novel class of inorganic materials in the field of separations and particularly adsorption. Owing to its high surface area and thermal stability, porous BN has been researched for CO2 capture and water cleaning, for instance. However, most research remains at laboratory scale due to a lack of understanding of the formation mechanism of porous BN, which is still largely a ‘black box’ and prevents scale-up. Partial reaction pathways have been unveiled, but they omit critical steps in the formation, including the porosity development, which is key to adsorption. To unlock the potential of porous BN at a larger scale, we have investigated its formation from the perspective of both chemical formation and porosity development. We have characterised reaction intermediates obtained at different temperatures with a range of analytical and spectroscopic tools. Using these analyses, we propose a mechanism that highlights the key stages of BN formation and its porosity, including the intermediates and gaseous species formed in the process. We identified that the formation of non-porous carbon nitride is crucial to form porous BN with release of porogens, such as HCN and CO2. This work paves the way for scaled-up processes to use porous BN to its full potential at industrial level for gas and liquid separations.
Preparation of phosphorus-doped boron nitride and its adsorption of heavy metals from flue gas
