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An amine-functionalized MIL-53 metal-organic framework with large separation power for CO2 and CH4.一种对二氧化碳和甲烷具有高分离能力的胺官能化MIL-53金属有机框架。
J Am Chem Soc. 2009 May 13;131(18):6326-7. doi: 10.1021/ja900555r.
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Control of pore size and functionality in isoreticular zeolitic imidazolate frameworks and their carbon dioxide selective capture properties.等规金属有机骨架材料中孔径和功能的调控及其二氧化碳选择性捕获性能
J Am Chem Soc. 2009 Mar 25;131(11):3875-7. doi: 10.1021/ja809459e.
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High-capacity methane storage in metal-organic frameworks M2(dhtp): the important role of open metal sites.金属有机框架材料M2(dhtp)中的高容量甲烷存储:开放金属位点的重要作用
J Am Chem Soc. 2009 Apr 8;131(13):4995-5000. doi: 10.1021/ja900258t.
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Adsorption properties and structure of CO2 adsorbed on open coordination sites of metal-organic framework Ni2(dhtp) from gas adsorption, IR spectroscopy and X-ray diffraction.通过气体吸附、红外光谱和X射线衍射研究金属有机框架Ni2(dhtp)开放配位位点上吸附的CO2的吸附特性和结构
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Enhanced H2 adsorption in isostructural metal-organic frameworks with open metal sites: strong dependence of the binding strength on metal ions.具有开放金属位点的同构金属有机框架中增强的H2吸附:结合强度对金属离子的强烈依赖性。
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Metal-organic frameworks with high capacity and selectivity for harmful gases.对有害气体具有高容量和选择性的金属有机框架。
Proc Natl Acad Sci U S A. 2008 Aug 19;105(33):11623-7. doi: 10.1073/pnas.0804900105. Epub 2008 Aug 18.
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Dramatic tuning of carbon dioxide uptake via metal substitution in a coordination polymer with cylindrical pores.通过在具有圆柱形孔的配位聚合物中进行金属取代对二氧化碳吸收进行显著调节。
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Exceptional behavior over the whole adsorption-storage-delivery cycle for NO in porous metal organic frameworks.多孔金属有机框架中一氧化氮在整个吸附-储存-释放循环过程中的优异表现。
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Colossal cages in zeolitic imidazolate frameworks as selective carbon dioxide reservoirs.沸石咪唑酯骨架材料中的巨大笼状结构作为选择性二氧化碳储存库。
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富含开放金属位点的金属-有机骨架实现二氧化碳的高效分离。

Highly efficient separation of carbon dioxide by a metal-organic framework replete with open metal sites.

机构信息

Center for Reticular Chemistry at the California NanoSystems Institute, Department of Chemistry and Biochemistry, University of California, 607 Charles E. Young Drive East, Los Angeles, CA 90095, USA.

出版信息

Proc Natl Acad Sci U S A. 2009 Dec 8;106(49):20637-40. doi: 10.1073/pnas.0909718106. Epub 2009 Nov 30.

DOI:10.1073/pnas.0909718106
PMID:19948967
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2791636/
Abstract

Selective capture of CO(2), which is essential for natural gas purification and CO(2) sequestration, has been reported in zeolites, porous membranes, and amine solutions. However, all such systems require substantial energy input for release of captured CO(2), leading to low energy efficiency and high cost. A new class of materials named metal-organic frameworks (MOFs) has also been demonstrated to take up voluminous amounts of CO(2). However, these studies have been largely limited to equilibrium uptake measurements, which are a poor predictor of separation ability, rather than the more industrially relevant kinetic (dynamic) capacity. Here, we report that a known MOF, Mg-MOF-74, with open magnesium sites, rivals competitive materials in CO(2) capture, with 8.9 wt. % dynamic capacity, and undergoes facile CO(2) release at significantly lower temperature, 80 degrees C. Mg-MOF-74 offers an excellent balance between dynamic capacity and regeneration. These results demonstrate the potential of MOFs with open metal sites as efficient CO(2) capture media.

摘要

已报道沸石、多孔膜和胺溶液等材料中存在 CO2 的选择性捕集,这对天然气的净化和 CO2 的封存至关重要。然而,所有这些系统在释放捕获的 CO2 时都需要大量的能量输入,导致能量效率低、成本高。一类名为金属有机骨架(MOF)的新型材料也被证明可以吸收大量的 CO2。然而,这些研究在很大程度上仅限于平衡吸收测量,这对于分离能力是一个很差的预测指标,而不是更具工业相关性的动力学(动态)容量。在这里,我们报告说,具有开放镁位的已知 MOF,Mg-MOF-74,在 CO2 捕获方面可与竞争性材料相媲美,具有 8.9wt%的动态容量,并且在明显更低的温度 80°C 下可轻松释放 CO2。Mg-MOF-74 在动态容量和再生之间具有极好的平衡。这些结果表明具有开放金属位的 MOFs 作为高效 CO2 捕获介质具有潜力。