CO2 Adsorption by Functionalized Nanoporous Materials: A Review

被引:99
|
作者
Gargiulo, Nicola [1 ]
Pepe, Francesco [2 ]
Caputo, Domenico [1 ]
机构
[1] Univ Naples Federico II, Dipartimento Ingn Chim Mat & Prod Ind, I-80125 Naples, Italy
[2] Univ Sannio, Dipartimento Ingn, I-82100 Benevento, Italy
关键词
Nanoporous Materials; Zeolites; Mesoporous Silicates; Metal Organic Frameworks; Functionalization; Cation Exchange; Amine Groups; CO2; Capture; Adsorption; METAL-ORGANIC FRAMEWORK; CARBON-DIOXIDE CAPTURE; MESOPOROUS MOLECULAR-SIEVES; EXCHANGED ZSM-5 ZEOLITES; PORE-EXPANDED MCM-41; X-ZEOLITES; FLUE-GAS; RETENTION CAPACITY; Y-ZEOLITES; CU-BTC;
D O I
10.1166/jnn.2014.8893
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This review highlights the recent advances in the development of functionalized nanoporous adsorbents for CO2 capture. Three main classes of materials are taken into account: zeolites, mesoporous silicates, and metal organic frameworks (MOFs). Proper modification of the cation content of zeolites, as well as the introduction of functional groups such as amine groups into ordered mesoporous silicates and MOFs, greatly enhance the CO2 adsorptive properties of these substrates. Specifically, cation-exchanged zeolites can be currently considered the benchmark for ordered nanoporous CO2 adsorbents, finding application also on a plant scale. Amino-functionalized mesoporous silicates tend to show a high affinity toward CO2: while this could be an advantage when pushed purification is needed, it also implies that full regeneration of the adsorbent can be achieved only by putting its surface in contact with a completely CO2-free environment. On the contrary, similarly modified MOFs show higher CO2 adsorption working capacities: this potentially makes them even better candidates than their mesoporous inorganic homologues for a plant scale use. However, the persisting lack of reliable methods for the pelletization of both ordered mesoporous silicates and MOFs creates a care for further development efforts in the next future.
引用
收藏
页码:1811 / 1822
页数:12
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