UTSA-16 Growth within 3D-Printed Co-Kaolin Monoliths with High Selectivity for CO2/CH4, CO2/N2, and CO2/H2 Separation

材料科学 选择性 化学工程 纳米技术 催化作用 有机化学 工程类 化学
作者
Shane Lawson,Qasim Al‐Naddaf,Anirduh Krishnamurthy,Marc St. Amour,Connor Griffin,Ali A. Rownaghi,James C. Knox,Fateme Rezaei
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:10 (22): 19076-19086 被引量:102
标识
DOI:10.1021/acsami.8b05192
摘要

Honeycomb monoliths loaded with metal-organic frameworks (MOFs) are highly desirable adsorption contactors because of their low-pressure drop, rapid mass-transfer kinetics, and high-adsorption capacity. Moreover, three-dimensional (3D)-printing technology renders direct material modification a realistic and economic prospect. In this study, 3D printing was utilized to impregnate kaolin-based monolith with UTSA-16 metal formation precursor (Co), whereupon an internal growth was facilitated via a solvothermal synthesis approach. The cobalt weight loading in the kaolin support was varied systematically to optimize the MOF growth while retaining monolith mechanical integrity. The obtained UTSA-16 monolith with 90 wt % loading exhibited similar textural features and adsorption characteristics to its powder analogue while improving upon structural integrity. In comparison to previously developed 3D-printed UTSA-16 monoliths, the UTSA-16-kaolin monolith not only showed higher MOF loading but also higher compression stress, indicative of its robust structure. Furthermore, the 3D-printed UTSA-16-kaolin monolith displayed a comparable CO2 adsorption capacity to the UTSA-16 powder (3.1 vs 3.5 mmol/g at 25 °C and 1 bar), which was proportional to its loading. Selectivity values of 49, 238, and 3725 were obtained for CO2/CH4, CO2/N2, and CO2/H2, respectively, demonstrating good separation potential of the 3D-printed MOF monolith for various gas mixtures, as determined by both equilibrium and dynamic adsorption measurements. Overall, this study provides a novel route for the fabrication of UTSA-16-loaded monoliths, which demonstrate both high MOF loading and mechanical integrity that could be readily applied to various CO2 capture applications.
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
1秒前
科目三应助科研通管家采纳,获得10
1秒前
1秒前
传奇3应助科研通管家采纳,获得10
1秒前
Copyright应助科研通管家采纳,获得10
1秒前
充电宝应助科研通管家采纳,获得10
1秒前
NexusExplorer应助科研通管家采纳,获得10
1秒前
1秒前
echo发布了新的文献求助10
2秒前
于熙源发布了新的文献求助20
3秒前
4秒前
科研通AI2S应助jiasuo采纳,获得10
4秒前
1111111111111发布了新的文献求助10
5秒前
gy完成签到,获得积分10
5秒前
银月追风发布了新的文献求助10
5秒前
浅影驳回了Hx应助
6秒前
英姑应助小猪妈妈采纳,获得10
8秒前
10秒前
10秒前
鱼山完成签到,获得积分10
10秒前
炙热宛秋关注了科研通微信公众号
11秒前
1111111111111完成签到,获得积分10
11秒前
三岁半完成签到,获得积分10
12秒前
13秒前
13秒前
搜集达人应助zhangbing采纳,获得10
15秒前
威武忆山完成签到 ,获得积分10
15秒前
Sirius完成签到,获得积分10
15秒前
Ava应助kyhoy采纳,获得10
16秒前
拼搏的土豆完成签到,获得积分10
16秒前
Jkaaaaaa发布了新的文献求助10
17秒前
在水一方应助echo采纳,获得10
17秒前
Daiweiwei发布了新的文献求助10
17秒前
cfjbxf发布了新的文献求助10
17秒前
18秒前
李健的小迷弟应助faye采纳,获得20
20秒前
面包骑士发布了新的文献求助10
20秒前
春实秋华完成签到,获得积分10
20秒前
20秒前
科研通AI6.3应助zz采纳,获得10
21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
Geist der Kunst und Kultur 1000
Resistance Spot Welding Dataset for Automobile Body-in-White Quality Analysis 748
悉尼大学博士学位论文,题目:Modelling and testing of one-sided stitched laminated composites. 作者:Kristopher P. Plain 700
Matrix Methods in Data Mining and Pattern Recognition Second Edition 510
丝光沸石活性位点定向调控及其二甲醚羰基化性能研究 500
Elgar Concise Encyclopedia of Research Methods in the Social Sciences 400
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 7415292
求助须知:如何正确求助?哪些是违规求助? 9018740
关于积分的说明 19212843
捐赠科研通 7046564
什么是DOI,文献DOI怎么找? 3234121
关于科研通互助平台的介绍 2396540
邀请新用户注册赠送积分活动 2216371