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CO在磷酸铝和硅磷酸铝分子筛上异常低的吸附热

Unusually Low Heat of Adsorption of CO on AlPO and SAPO Molecular Sieves.

作者信息

Pérez-Botella Eduardo, Martínez-Franco Raquel, González-Camuñas Nuria, Cantín Ángel, Palomino Miguel, Moliner Manuel, Valencia Susana, Rey Fernando

机构信息

Instituto de Tecnología Química, Universitat Politècnica de València-Consejo Superior de Investigaciones Científicas, Valencia, Spain.

Institut Français du Pétrole (IFP) Energies Nouvelles, Lyon, France.

出版信息

Front Chem. 2020 Oct 28;8:588712. doi: 10.3389/fchem.2020.588712. eCollection 2020.

DOI:10.3389/fchem.2020.588712
PMID:33195090
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7655961/
Abstract

The capture of CO from post-combustion streams or from other mixtures, such as natural gas, is an effective way of reducing CO emissions, which contribute to the greenhouse effect in the atmosphere. One of the developing technologies for this purpose is physisorption on selective solid adsorbents. The ideal adsorbents are selective toward CO, have a large adsorption capacity at atmospheric pressure and are easily regenerated, resulting in high working capacity. Therefore, adsorbents combining molecular sieving properties and low heats of adsorption of CO are of clear interest as they will provide high selectivities and regenerabilities in CO separation process. Here we report that some aluminophosphate (AlPO) and silicoaluminophosphate (SAPO) materials with LTA, CHA and AFI structures present lower heats of adsorption of CO (13-25 kJ/mol) than their structurally analogous zeolites at comparable framework charges. In some cases, their heats of adsorption are even lower than those of pure silica composition (20-25 kJ/mol). This could mean a great improvement in the regeneration process compared to the most frequently used zeolitic adsorbents for this application while maintaining most of their adsorption capacity, if materials with the right stability and pore size and topology are found.

摘要

从燃烧后气流或其他混合物(如天然气)中捕获一氧化碳(CO)是减少CO排放的有效方法,CO排放会导致大气中的温室效应。为此目的,一种正在发展的技术是在选择性固体吸附剂上进行物理吸附。理想的吸附剂对CO具有选择性,在大气压下具有大的吸附容量且易于再生,从而具有高的工作容量。因此,兼具分子筛性能和低CO吸附热的吸附剂显然备受关注,因为它们将在CO分离过程中提供高选择性和可再生性。在此我们报告,一些具有LTA、CHA和AFI结构的铝磷酸盐(AlPO)和硅铝磷酸盐(SAPO)材料在可比的骨架电荷下,其CO吸附热(13 - 25 kJ/mol)低于其结构类似的沸石。在某些情况下,它们的吸附热甚至低于纯硅组成的材料(20 - 25 kJ/mol)。如果找到具有合适稳定性、孔径和拓扑结构的材料,与该应用中最常用的沸石吸附剂相比,这可能意味着再生过程有很大改进,同时保持其大部分吸附容量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb70/7655961/0bd7681be44e/fchem-08-588712-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb70/7655961/670188ac0293/fchem-08-588712-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb70/7655961/7ecd7533c97b/fchem-08-588712-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb70/7655961/21a437ba94d1/fchem-08-588712-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb70/7655961/0bd7681be44e/fchem-08-588712-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb70/7655961/670188ac0293/fchem-08-588712-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb70/7655961/7ecd7533c97b/fchem-08-588712-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb70/7655961/21a437ba94d1/fchem-08-588712-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb70/7655961/0bd7681be44e/fchem-08-588712-g0004.jpg

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引用本文的文献

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本文引用的文献

1
Computational evaluation of aluminophosphate zeotypes for CO/N separation.用于CO/N分离的磷酸铝沸石型材料的计算评估
Phys Chem Chem Phys. 2017 Aug 30;19(34):22801-22812. doi: 10.1039/c7cp03841k.
2
Molecular basis for the high CO2 adsorption capacity of chabazite zeolites.菱沸石对高二氧化碳吸附容量的分子基础
ChemSusChem. 2014 Nov;7(11):3031-8. doi: 10.1002/cssc.201402555. Epub 2014 Oct 1.
3
Discriminative separation of gases by a "molecular trapdoor" mechanism in chabazite zeolites.通过方沸石沸石中的“分子活门”机制对气体进行有区别的分离。
J Am Chem Soc. 2012 Nov 21;134(46):19246-53. doi: 10.1021/ja309274y. Epub 2012 Nov 13.
4
New insights on CO2-methane separation using LTA zeolites with different Si/Al ratios and a first comparison with MOFs.关于使用不同 Si/Al 比的 LTA 沸石和 MOFs 进行 CO2-甲烷分离的新见解。
Langmuir. 2010 Feb 2;26(3):1910-7. doi: 10.1021/la9026656.
5
Supramolecular self-assembled molecules as organic directing agent for synthesis of zeolites.超分子自组装分子作为沸石合成的有机导向剂。
Nature. 2004 Sep 16;431(7006):287-90. doi: 10.1038/nature02909.