Selective and adsorptive removal of anionic dyes and CO2 with azolium-based metal-organic frameworks; Journal of Colloid and Interface Science; Vol. 519

Bibliographic Details
Parent link:Journal of Colloid and Interface Science
Vol. 519.— 2018.— [P. 214-223]
Corporate Author: Национальный исследовательский Томский политехнический университет Исследовательская школа химических и биомедицинских технологий (ИШХБМТ)
Other Authors: Chizoba I. E. Ezugwu, Md. Ali Asraf, Xiao Li, Liu Shengwei, Kao Chih-Ming, Zhuiykov S. V. Sergey, Verpoort F. V. K. Frensis Valter Kornelius
Summary:Title screen
The positively charged azolium moieties make imidazolium linker an ideal linker for the construction of cationic metal-organic frameworks because the ligand induces cationic environments in the frameworks. Therefore, we employed two imidazolium ligands, 1,3-bis(4-carboxyphenyl)imidazolium chloride (H2L+ Cl) and 1,3-bis(3,5-dicarboxyphenyl)imidazolium chloride (H4L+ Cl), to synthesize two nickel azolium-based MOFs, 1 and 2. The as-synthesis MOFs were characterized by PXRD, TGA, FE-SEM, HRTEM, FTIR and BET measurements. By applying 1 and 2 in liquid phase adsorption of charged molecules of dyes, they successfully exhibit remarkable efficiency for adsorptive removal of anionic dyes, Methyl orange (MO), Congo red (CR), and Orange II sodium salt (OS), from aqueous solution. The framework proves efficient in photocatalytic degradation of anionic dye. Furthermore, in the gaseous phase adsorption, 1 and 2 selectively adsorb CO2 over CH4 due to the higher quadrupole moment of CO2. Overall, the results show that azolium-based MOFs have potential applications for adsorptive removal of charged organic contaminants from both aqueous and gaseous environment.
Режим доступа: по договору с организацией-держателем ресурса
Language:English
Published: 2018
Subjects:
Online Access:https://doi.org/10.1016/j.jcis.2018.02.003
Format: MixedMaterials Electronic Book Chapter
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=657869

MARC

LEADER 00000naa0a2200000 4500
001 657869
005 20250123155429.0
035 |a (RuTPU)RU\TPU\network\24686 
035 |a RU\TPU\network\24493 
090 |a 657869 
100 |a 20180327d2018 k||y0engy50 ba 
101 0 |a eng 
102 |a US 
135 |a drcn ---uucaa 
181 0 |a i  
182 0 |a b 
200 1 |a Selective and adsorptive removal of anionic dyes and CO2 with azolium-based metal-organic frameworks  |f I. E. Chizoba, Md. Ali Asraf, Xiao Li [et al.] 
203 |a Text  |c electronic 
300 |a Title screen 
320 |a [References: p. 222-223 (53 tit.)] 
330 |a The positively charged azolium moieties make imidazolium linker an ideal linker for the construction of cationic metal-organic frameworks because the ligand induces cationic environments in the frameworks. Therefore, we employed two imidazolium ligands, 1,3-bis(4-carboxyphenyl)imidazolium chloride (H2L+ Cl) and 1,3-bis(3,5-dicarboxyphenyl)imidazolium chloride (H4L+ Cl), to synthesize two nickel azolium-based MOFs, 1 and 2. The as-synthesis MOFs were characterized by PXRD, TGA, FE-SEM, HRTEM, FTIR and BET measurements. By applying 1 and 2 in liquid phase adsorption of charged molecules of dyes, they successfully exhibit remarkable efficiency for adsorptive removal of anionic dyes, Methyl orange (MO), Congo red (CR), and Orange II sodium salt (OS), from aqueous solution. The framework proves efficient in photocatalytic degradation of anionic dye. Furthermore, in the gaseous phase adsorption, 1 and 2 selectively adsorb CO2 over CH4 due to the higher quadrupole moment of CO2. Overall, the results show that azolium-based MOFs have potential applications for adsorptive removal of charged organic contaminants from both aqueous and gaseous environment. 
333 |a Режим доступа: по договору с организацией-держателем ресурса 
461 |t Journal of Colloid and Interface Science 
463 |t Vol. 519  |v [P. 214-223]  |d 2018 
610 1 |a электронный ресурс 
610 1 |a труды учёных ТПУ 
610 1 |a dye 
610 1 |a gaseous molecule 
610 1 |a adsorption 
610 1 |a photocatalysis 
610 1 |a красители 
610 1 |a адсорбция 
610 1 |a фотокатализ 
701 1 |a Chizoba  |b I. E.  |g Ezugwu 
701 0 |a Md. Ali Asraf 
701 0 |a Xiao Li 
701 0 |a Liu Shengwei 
701 0 |a Kao Chih-Ming 
701 1 |a Zhuiykov  |b S. V.  |g Sergey 
701 1 |a Verpoort  |b F. V. K.  |c Chemical Engineer  |c Professor of Tomsk Polytechnic University, doctor of chemical Sciences  |f 1963-  |g Frensis Valter Kornelius  |3 (RuTPU)RU\TPU\pers\35059  |9 18334 
712 0 2 |a Национальный исследовательский Томский политехнический университет  |b Исследовательская школа химических и биомедицинских технологий (ИШХБМТ)  |c (2017- )  |3 (RuTPU)RU\TPU\col\23537 
801 2 |a RU  |b 63413507  |c 20221114  |g RCR 
856 4 |u https://doi.org/10.1016/j.jcis.2018.02.003 
942 |c CF