渗透
选择性
膜
氢
渗透
聚酰亚胺
化学工程
材料科学
石墨烯
磁导率
脱氢
气体分离
开裂
化学
基质(化学分析)
氢气净化器
聚醚酰亚胺
膜技术
合成膜
聚合物
还原(数学)
纳米复合材料
锗
作者
Soon Hyeong So,Sunwoo Kim,Minsu Kim,Donghyun Kim,Donghyun Kim,Taehwan Kim,Kiwon Eum,Yun Ho Kim,Junghwan Kim,Dae Woo Kim,Dae Woo Kim
出处
期刊:Science Advances
[American Association for the Advancement of Science]
日期:2026-02-18
卷期号:12 (8): eaeb4360-eaeb4360
标识
DOI:10.1126/sciadv.aeb4360
摘要
We report the application of mixed-matrix membranes for high-temperature hydrogen separation. To enhance hydrogen selectivity, graphene nanoribbons (GNRs) were incorporated into ZIF-8 fillers, forming a physically confined structure conducive to hydrogen transport. The metal-organic framework (MOF)/GNR filler embedded into a polyimide (PI) matrix yielded a much higher H 2 permeability (298 Barrer, +40%) and H 2 /N 2 selectivity (15, +25%) than the neat PI membrane. In particular, the as-prepared asymmetric membrane achieved a H 2 permeance of 212 ± 45 Gas Permeation Unit (GPU) and H 2 /N 2 selectivity of 19 ± 2 at 35°C. Remarkably, at 300°C, the H 2 permeance rose to 775 ± 139 GPU while maintaining a H 2 /N 2 selectivity of 13 ± 1, outperforming polymer-based membranes. A techno-economic analysis of an NH 3 cracking process demonstrated that this high permeance reduces membrane area requirements by 68.2% and lowers H 2 separation costs by 35.1% compared with operation at 35°C, leading to a 9.8% reduction in the levelized cost of hydrogen.
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