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Hydrophobic shell structured NH2-MIL(Ti)-125@mesoporous carbon composite via confined growth strategy for ultra-high selective adsorption of toluene under highly humid environment

[Display omitted] •NH2-MIL(Ti)-125 was confined grown into via ‘ship-in-the-bottle’ synthesis approach by Ti-clusters anchored OMC.•Hydrophobic shell (OMC) enhanced surface non-polar and humidity resistance on MIL(Ti)@OMCTi.•MIL(Ti)@OMCTi achieved interconnected micro-/mesoporous networks and accele...

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Published in:Chemical engineering journal (Lausanne, Switzerland : 1996) Switzerland : 1996), 2022-03, Vol.432, p.134340, Article 134340
Main Authors: Gao, Zhu, Wang, Jiaxing, Muhammad, Yaseen, Hu, Peng, Hu, Yang, Chu, Zhe, Zhao, Zhongxing, Zhao, Zhenxia
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container_title Chemical engineering journal (Lausanne, Switzerland : 1996)
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Wang, Jiaxing
Muhammad, Yaseen
Hu, Peng
Hu, Yang
Chu, Zhe
Zhao, Zhongxing
Zhao, Zhenxia
description [Display omitted] •NH2-MIL(Ti)-125 was confined grown into via ‘ship-in-the-bottle’ synthesis approach by Ti-clusters anchored OMC.•Hydrophobic shell (OMC) enhanced surface non-polar and humidity resistance on MIL(Ti)@OMCTi.•MIL(Ti)@OMCTi achieved interconnected micro-/mesoporous networks and accelerated mass transfer.•MIL(Ti)@OMCTi showed high moisture-resistance and adsorption affinity for toluene at ultra-low pressure.•the mechanism of selective toluene adsorption and recycling performance were deeply investigated. Competitive adsorption of volatile organic compounds (VOCs) under high humidity is a critical but challenging issue in the applications of metal–organic frameworks (MOFs). In this work, hydrophobic-shell structured NH2-MIL(Ti)-125@mesoporous carbon composite was designed to enhance selective adsorption towards VOCs under humid conditions via confined growth strategy. Ti-clusters were first anchored into pores of ordered mesoporous carbon (OMC), and then confined grown into NH2-MIL(Ti)-125 via ‘ship-in-the-bottle’ approach. Hydrophobic shell of OMC concurrently protected the adsorption sites on NH2-MIL(Ti)-125 from H2O occupation and enhanced affinity towards non-polar toluene. Moreover, the resulting composited supplied abundant diffusion channels for toluene thereby accelerated the mass transfer though mesopores (OMC) and micropores (MOFs). As expected, the hydrophobic-shell NH2-MIL(Ti)-125@OMC composite efficiently enhanced hydrophobic property and toluene adsorption affinity. It obtained a dramatical increase in toluene adsorption capacity (3.86 mmol/g at 0.001P/P0) about 7.4 times of NH2-MIL(Ti)-125, and a 29% decrease in water vapor adsorption capacity (0.30 g/g at 1 mbar), which much superior than many reported expensive adsorbents. In addition, the composite induced more confined micropores to mesopores interconnected structure in MIL(Ti)@OMCTi, and hence facilitated toluene diffusion. The toluene rate constant of pseudo-second-order adsorption (ka) on the MIL(Ti)@OMCTi was up to 0.12 g/(mmol∙min), which was 1.2–2.0 times higher than those of the MIL(Ti) species. Moreover, breakthrough curve indicated that MIL(Ti)@OMCTi showed 1.5 times of toluene working capacity with faster diffusivity at 80% RH compared to pure NH2-MIL(Ti)-125, while the latter exhibited much lower value of Qw/Qe than that of the former. This work provides a novel composite strategy for hydrophobic MOFs construction, and deeper understanding for VOCs/H2O competitive
doi_str_mv 10.1016/j.cej.2021.134340
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Competitive adsorption of volatile organic compounds (VOCs) under high humidity is a critical but challenging issue in the applications of metal–organic frameworks (MOFs). In this work, hydrophobic-shell structured NH2-MIL(Ti)-125@mesoporous carbon composite was designed to enhance selective adsorption towards VOCs under humid conditions via confined growth strategy. Ti-clusters were first anchored into pores of ordered mesoporous carbon (OMC), and then confined grown into NH2-MIL(Ti)-125 via ‘ship-in-the-bottle’ approach. Hydrophobic shell of OMC concurrently protected the adsorption sites on NH2-MIL(Ti)-125 from H2O occupation and enhanced affinity towards non-polar toluene. Moreover, the resulting composited supplied abundant diffusion channels for toluene thereby accelerated the mass transfer though mesopores (OMC) and micropores (MOFs). As expected, the hydrophobic-shell NH2-MIL(Ti)-125@OMC composite efficiently enhanced hydrophobic property and toluene adsorption affinity. It obtained a dramatical increase in toluene adsorption capacity (3.86 mmol/g at 0.001P/P0) about 7.4 times of NH2-MIL(Ti)-125, and a 29% decrease in water vapor adsorption capacity (0.30 g/g at 1 mbar), which much superior than many reported expensive adsorbents. In addition, the composite induced more confined micropores to mesopores interconnected structure in MIL(Ti)@OMCTi, and hence facilitated toluene diffusion. The toluene rate constant of pseudo-second-order adsorption (ka) on the MIL(Ti)@OMCTi was up to 0.12 g/(mmol∙min), which was 1.2–2.0 times higher than those of the MIL(Ti) species. Moreover, breakthrough curve indicated that MIL(Ti)@OMCTi showed 1.5 times of toluene working capacity with faster diffusivity at 80% RH compared to pure NH2-MIL(Ti)-125, while the latter exhibited much lower value of Qw/Qe than that of the former. 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Competitive adsorption of volatile organic compounds (VOCs) under high humidity is a critical but challenging issue in the applications of metal–organic frameworks (MOFs). In this work, hydrophobic-shell structured NH2-MIL(Ti)-125@mesoporous carbon composite was designed to enhance selective adsorption towards VOCs under humid conditions via confined growth strategy. Ti-clusters were first anchored into pores of ordered mesoporous carbon (OMC), and then confined grown into NH2-MIL(Ti)-125 via ‘ship-in-the-bottle’ approach. Hydrophobic shell of OMC concurrently protected the adsorption sites on NH2-MIL(Ti)-125 from H2O occupation and enhanced affinity towards non-polar toluene. Moreover, the resulting composited supplied abundant diffusion channels for toluene thereby accelerated the mass transfer though mesopores (OMC) and micropores (MOFs). As expected, the hydrophobic-shell NH2-MIL(Ti)-125@OMC composite efficiently enhanced hydrophobic property and toluene adsorption affinity. It obtained a dramatical increase in toluene adsorption capacity (3.86 mmol/g at 0.001P/P0) about 7.4 times of NH2-MIL(Ti)-125, and a 29% decrease in water vapor adsorption capacity (0.30 g/g at 1 mbar), which much superior than many reported expensive adsorbents. In addition, the composite induced more confined micropores to mesopores interconnected structure in MIL(Ti)@OMCTi, and hence facilitated toluene diffusion. The toluene rate constant of pseudo-second-order adsorption (ka) on the MIL(Ti)@OMCTi was up to 0.12 g/(mmol∙min), which was 1.2–2.0 times higher than those of the MIL(Ti) species. Moreover, breakthrough curve indicated that MIL(Ti)@OMCTi showed 1.5 times of toluene working capacity with faster diffusivity at 80% RH compared to pure NH2-MIL(Ti)-125, while the latter exhibited much lower value of Qw/Qe than that of the former. 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Competitive adsorption of volatile organic compounds (VOCs) under high humidity is a critical but challenging issue in the applications of metal–organic frameworks (MOFs). In this work, hydrophobic-shell structured NH2-MIL(Ti)-125@mesoporous carbon composite was designed to enhance selective adsorption towards VOCs under humid conditions via confined growth strategy. Ti-clusters were first anchored into pores of ordered mesoporous carbon (OMC), and then confined grown into NH2-MIL(Ti)-125 via ‘ship-in-the-bottle’ approach. Hydrophobic shell of OMC concurrently protected the adsorption sites on NH2-MIL(Ti)-125 from H2O occupation and enhanced affinity towards non-polar toluene. Moreover, the resulting composited supplied abundant diffusion channels for toluene thereby accelerated the mass transfer though mesopores (OMC) and micropores (MOFs). As expected, the hydrophobic-shell NH2-MIL(Ti)-125@OMC composite efficiently enhanced hydrophobic property and toluene adsorption affinity. It obtained a dramatical increase in toluene adsorption capacity (3.86 mmol/g at 0.001P/P0) about 7.4 times of NH2-MIL(Ti)-125, and a 29% decrease in water vapor adsorption capacity (0.30 g/g at 1 mbar), which much superior than many reported expensive adsorbents. In addition, the composite induced more confined micropores to mesopores interconnected structure in MIL(Ti)@OMCTi, and hence facilitated toluene diffusion. The toluene rate constant of pseudo-second-order adsorption (ka) on the MIL(Ti)@OMCTi was up to 0.12 g/(mmol∙min), which was 1.2–2.0 times higher than those of the MIL(Ti) species. Moreover, breakthrough curve indicated that MIL(Ti)@OMCTi showed 1.5 times of toluene working capacity with faster diffusivity at 80% RH compared to pure NH2-MIL(Ti)-125, while the latter exhibited much lower value of Qw/Qe than that of the former. This work provides a novel composite strategy for hydrophobic MOFs construction, and deeper understanding for VOCs/H2O competitive adsorption on MOFs composites in large scale applications.</abstract><pub>Elsevier B.V</pub><doi>10.1016/j.cej.2021.134340</doi></addata></record>
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ispartof Chemical engineering journal (Lausanne, Switzerland : 1996), 2022-03, Vol.432, p.134340, Article 134340
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subjects Confined MOF growth
Humid condition
Hydrophobic protective carapace
NH2-MIL(Ti)-125 composite
Toluene adsorption
title Hydrophobic shell structured NH2-MIL(Ti)-125@mesoporous carbon composite via confined growth strategy for ultra-high selective adsorption of toluene under highly humid environment
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