Suppr超能文献

探究碳材料中小于 5 埃的微孔以实现精准的低碳烯烃/烷烃分离。

Probing sub-5 Ångstrom micropores in carbon for precise light olefin/paraffin separation.

机构信息

School of Chemistry and Chemical Engineering, South China University of Technology, Guangzhou, China.

Materials Science and Technology Division, Oak Ridge National Laboratory, Oak Ridge, TN, USA.

出版信息

Nat Commun. 2023 Mar 2;14(1):1197. doi: 10.1038/s41467-023-36890-6.

Abstract

Olefin/paraffin separation is an important but challenging and energy-intensive process in petrochemical industry. The realization of carbons with size-exclusion capability is highly desirable but rarely reported. Herein, we report polydopamine-derived carbons (PDA-Cx, where x refers to the pyrolysis temperature) with tailorable sub-5 Å micropore orifices together with larger microvoids by one-step pyrolysis. The sub-5 Å micropore orifices centered at 4.1-4.3 Å in PDA-C800 and 3.7-4.0 Å in PDA-C900 allow the entry of olefins while entirely excluding their paraffin counterparts, performing a precise cut-off to discriminate olefin/paraffin with sub-angstrom discrepancy. The larger voids enable high CH and CH capacities of 2.25 and 1.98 mmol g under ambient conditions, respectively. Breakthrough experiments confirm that a one-step adsorption-desorption process can obtain high-purity olefins. Inelastic neutron scattering further reveals the host-guest interaction of adsorbed CH and CH molecules in PDA-Cx. This study opens an avenue to exploit the sub-5 Å micropores in carbon and their desirable size-exclusion effect.

摘要

烯烃/烷烃分离是石油化工行业中一个重要但具有挑战性和能源密集型的过程。实现具有尺寸排阻能力的碳材料是非常理想的,但很少有报道。在此,我们报道了一种通过一步热解得到的具有可调节的亚 5Å 微孔口和较大微孔的聚多巴胺衍生碳(PDA-Cx,其中 x 表示热解温度)。在 PDA-C800 中,亚 5Å 的微孔口中心位于 4.1-4.3Å,在 PDA-C900 中,微孔口中心位于 3.7-4.0Å,允许烯烃进入,而完全排斥其对应的烷烃,实现了对亚 Å 差异的烯烃/烷烃的精确截断。较大的空隙使 PDA-Cx 在环境条件下分别具有 2.25 和 1.98mmol/g 的高 CH 和 CH 容量。突破实验证实,一步吸附-解吸过程可以获得高纯度的烯烃。非弹性中子散射进一步揭示了吸附的 CH 和 CH 分子在 PDA-Cx 中的主客体相互作用。这项研究为利用碳材料中的亚 5Å 微孔及其理想的尺寸排阻效应开辟了一条途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e818/9981619/0d58a08c6511/41467_2023_36890_Fig1_HTML.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验