X射线光电子能谱
吸附
介质阻挡放电
等离子体
化学吸附
多孔性
大气压力
氨
材料科学
大气压等离子体
碳纤维
化学工程
非热等离子体
电介质
分析化学(期刊)
化学
环境化学
复合材料
复合数
有机化学
光电子学
物理
地质学
工程类
海洋学
量子力学
作者
Madhuwanthi Buddhadasa,Brieuc Verougstraete,Yamid Gomez-Rueda,David Petitjean,Joeri Denayer,François Reniers
标识
DOI:10.1016/j.jcou.2022.102388
摘要
Owing to its high porosity and tunable surface chemistry activated carbon (AC) is considered a promising material for CO2 adsorption. Functionalising porous materials by plasma is challenging but if successful, it could enhance the CO2 uptake capacity of AC via chemisorption. This work presents an in-depth analysis of the interactions between ammonia plasmas and the porous surface of AC monolithic samples. The treatment involved an ammonia based atmospheric-pressure dielectric barrier discharge and a low-pressure radio frequency plasma. Unique plasma reactor designs for treating 3-dimensional, electrically conducting and non-conducting monolithic structures at atmospheric pressure with versatile applications are presented. The plasma-surface interactions were analysed using emission spectroscopy and X-ray photoelectron spectroscopy. High surface N containing AC samples were then used to assess the treatment effect on the subsurface. A much lower although a still significant amount of N was found at depths of ∼30 µm. A simple fit of the results showed that the ratio of plasma species reaching the surface with higher to lower sticking probability was 4:1. A slight decrease in the microporosity of the plasma treated samples was found and attributed to pore blocking by the grafted N species. Plasma treated AC with high N showed an improved CO2 adsorption capacity of up to 14 % and selectivity against CH4 and N2 adsorption showed that the treatment was selective primarily towards CO2.
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