Boosting the CO2 adsorption performance by defect-rich hierarchical porous Mg-MOF-74

吸附 烟气 多孔性 金属有机骨架 介孔材料 化学工程 选择性 化学 活性炭 配体(生物化学) 材料科学 无机化学 有机化学 催化作用 受体 工程类 生物化学
作者
Haifei An,Weijian Tian,Xin Lü,Huanmei Yuan,Liyun Yang,Hao Zhang,Haoming Shen,Hao Bai
出处
期刊:Chemical Engineering Journal [Elsevier BV]
卷期号:469: 144052-144052 被引量:109
标识
DOI:10.1016/j.cej.2023.144052
摘要

Adsorbents with high adsorption capacity and high selectivity are crucial for carbon capture, utilization and storage (CCUS) technology applied to industrial flue gas to reduce carbon emissions. In this paper, a defect-rich hierarchical porous Mg-MOF-74 was synthesized successfully with MgCl2·6H2O used as a metal source considering that the weak coordination of Cl− may interfere with the normal coordination process of metal centers and organic ligands, which causes the formation of crystal defects. Through the analysis of a series of characterizations, ligand deletion of Mg-MOF-74 prepared with MgCl2·6H2O was confirmed, and the deleted ligand was estimated to be approximately 20% compared with the traditional Mg-MOF-74 prepared with Mg(NO3)2·6H2O, which led to mesopores accounting for 36.9%, and the width of mesopores reached 13.1 nm. Compared with traditional Mg-MOF-74, the adsorption heat of CO2 at zero load of the defect-rich hierarchical porous Mg-MOF-74 increased from 36 kJ·mol−1 to 46 kJ·mol−1, and the saturated adsorption capacity of CO2 under ambient pressure was improved by 15%. Interestingly, the IAST selective adsorption performance of CO2/N2 was increased by 20 times. Compared with the saturated adsorption capacity for traditional Mg-MOF-74, the equivalent adsorption capacity of hierarchical porous Mg-MOF-74 only needs 17 kPa, indicating that it is suitable for carbon capture operation in a real flue environment. Calculations of density functional theory (DFT) confirmed that the active site of the hierarchical porous Mg-MOF-74 has a lower adsorption energy with CO2 due to the presence of defects, which is regarded to play a key role in improving the CO2 capture performance.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
dan完成签到,获得积分20
刚刚
刚刚
1秒前
1秒前
ning完成签到,获得积分20
1秒前
Starry完成签到 ,获得积分10
2秒前
乐正海亦完成签到,获得积分10
2秒前
anian发布了新的文献求助10
2秒前
淡淡梦容发布了新的文献求助10
3秒前
ASSA应助cxh采纳,获得10
3秒前
chancy完成签到,获得积分10
4秒前
Rainbow发布了新的文献求助10
4秒前
英姑应助摇铃牵风采纳,获得10
5秒前
yjj6809完成签到,获得积分10
5秒前
正直的幻竹完成签到,获得积分10
5秒前
心灵美的幼蓉完成签到,获得积分10
6秒前
西猫完成签到 ,获得积分10
6秒前
ding应助dxy采纳,获得30
6秒前
繁荣的傲南完成签到,获得积分10
7秒前
zyz完成签到,获得积分10
7秒前
Agoni完成签到,获得积分10
7秒前
冥土追魂完成签到,获得积分10
8秒前
淡淡梦容完成签到,获得积分10
8秒前
可爱的函函应助Mehah_n9采纳,获得10
8秒前
manman完成签到,获得积分10
8秒前
好运偏爱的那个男的完成签到,获得积分10
8秒前
阿六儿完成签到,获得积分10
8秒前
朴素蓝完成签到 ,获得积分10
9秒前
昴宿缉拿发布了新的文献求助10
9秒前
9秒前
9秒前
深情丸子完成签到 ,获得积分10
10秒前
wt发布了新的文献求助30
10秒前
11秒前
丢一池月光完成签到,获得积分10
12秒前
丘比特应助STP顶峰相见采纳,获得10
12秒前
kexing完成签到,获得积分10
13秒前
ambition应助anian采纳,获得10
13秒前
实验混子完成签到,获得积分10
14秒前
小涵发布了新的文献求助10
15秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Römisch-Germanische Forschungen 1000
Social Psychology (第二版) 700
China Pluperfect I: Epistemology of Past and Outside in Chinese Art 520
Matrix Methods in Data Mining and Pattern Recognition Second Edition 510
The fast track to determining transfer functions of linear circuits: The student guide 500
The Analytical and Numerical Solution of Electric and Magnetic Fields 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7613366
求助须知:如何正确求助?哪些是违规求助? 9188698
关于积分的说明 19685602
捐赠科研通 7186450
什么是DOI,文献DOI怎么找? 3270810
关于科研通互助平台的介绍 2434381
邀请新用户注册赠送积分活动 2265766