Functional Porous Organic Polymers with Conjugated Triaryl Triazine as the Core for Superfast Adsorption Removal of Organic Dyes
Developing efficient adsorbents for the removal of water pollutants is of great significance for environmental protection. In this study, conjugated triaryl triazines (CTT), containing intramolecular hydrogen-bonding patterns, were recognized to be intriguing building blocks for the construction of...
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Published in | ACS applied materials & interfaces Vol. 13; no. 5; pp. 6359 - 6366 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
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United States
American Chemical Society
10.02.2021
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Abstract | Developing efficient adsorbents for the removal of water pollutants is of great significance for environmental protection. In this study, conjugated triaryl triazines (CTT), containing intramolecular hydrogen-bonding patterns, were recognized to be intriguing building blocks for the construction of porous organic polymer (POP) adsorbents. These planar monomers with multiple phenolic hydroxyl groups facilitated the formation of aza-linked polymers with hierarchical porous structures, sheet-like morphology, good surface wettability, and high degree of functionality. Such structural characteristics of the CTT-POP adsorbents provided superfast adsorption of various cationic dyes from water. For the adsorption of methylene blue dye, the pseudo-second-order rate constant of CTT-POP-1 is 12.9 g mg–1 min–1, superior to those reported in the existing literature. In addition, CTT-POP-1 can be regenerated at least seven times with no loss in performance, indicating its potential application in water treatment. |
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AbstractList | Developing efficient adsorbents for the removal of water pollutants is of great significance for environmental protection. In this study, conjugated triaryl triazines (CTT), containing intramolecular hydrogen-bonding patterns, were recognized to be intriguing building blocks for the construction of porous organic polymer (POP) adsorbents. These planar monomers with multiple phenolic hydroxyl groups facilitated the formation of aza-linked polymers with hierarchical porous structures, sheet-like morphology, good surface wettability, and high degree of functionality. Such structural characteristics of the CTT-POP adsorbents provided superfast adsorption of various cationic dyes from water. For the adsorption of methylene blue dye, the pseudo-second-order rate constant of CTT-POP-1 is 12.9 g mg
min
, superior to those reported in the existing literature. In addition, CTT-POP-1 can be regenerated at least seven times with no loss in performance, indicating its potential application in water treatment. Developing efficient adsorbents for the removal of water pollutants is of great significance for environmental protection. In this study, conjugated triaryl triazines (CTT), containing intramolecular hydrogen-bonding patterns, were recognized to be intriguing building blocks for the construction of porous organic polymer (POP) adsorbents. These planar monomers with multiple phenolic hydroxyl groups facilitated the formation of aza-linked polymers with hierarchical porous structures, sheet-like morphology, good surface wettability, and high degree of functionality. Such structural characteristics of the CTT-POP adsorbents provided superfast adsorption of various cationic dyes from water. For the adsorption of methylene blue dye, the pseudo-second-order rate constant of CTT-POP-1 is 12.9 g mg–¹ min–¹, superior to those reported in the existing literature. In addition, CTT-POP-1 can be regenerated at least seven times with no loss in performance, indicating its potential application in water treatment. Developing efficient adsorbents for the removal of water pollutants is of great significance for environmental protection. In this study, conjugated triaryl triazines (CTT), containing intramolecular hydrogen-bonding patterns, were recognized to be intriguing building blocks for the construction of porous organic polymer (POP) adsorbents. These planar monomers with multiple phenolic hydroxyl groups facilitated the formation of aza-linked polymers with hierarchical porous structures, sheet-like morphology, good surface wettability, and high degree of functionality. Such structural characteristics of the CTT-POP adsorbents provided superfast adsorption of various cationic dyes from water. For the adsorption of methylene blue dye, the pseudo-second-order rate constant of CTT-POP-1 is 12.9 g mg–1 min–1, superior to those reported in the existing literature. In addition, CTT-POP-1 can be regenerated at least seven times with no loss in performance, indicating its potential application in water treatment. Developing efficient adsorbents for the removal of water pollutants is of great significance for environmental protection. In this study, conjugated triaryl triazines (CTT), containing intramolecular hydrogen-bonding patterns, were recognized to be intriguing building blocks for the construction of porous organic polymer (POP) adsorbents. These planar monomers with multiple phenolic hydroxyl groups facilitated the formation of aza-linked polymers with hierarchical porous structures, sheet-like morphology, good surface wettability, and high degree of functionality. Such structural characteristics of the CTT-POP adsorbents provided superfast adsorption of various cationic dyes from water. For the adsorption of methylene blue dye, the pseudo-second-order rate constant of CTT-POP-1 is 12.9 g mg-1 min-1, superior to those reported in the existing literature. In addition, CTT-POP-1 can be regenerated at least seven times with no loss in performance, indicating its potential application in water treatment.Developing efficient adsorbents for the removal of water pollutants is of great significance for environmental protection. In this study, conjugated triaryl triazines (CTT), containing intramolecular hydrogen-bonding patterns, were recognized to be intriguing building blocks for the construction of porous organic polymer (POP) adsorbents. These planar monomers with multiple phenolic hydroxyl groups facilitated the formation of aza-linked polymers with hierarchical porous structures, sheet-like morphology, good surface wettability, and high degree of functionality. Such structural characteristics of the CTT-POP adsorbents provided superfast adsorption of various cationic dyes from water. For the adsorption of methylene blue dye, the pseudo-second-order rate constant of CTT-POP-1 is 12.9 g mg-1 min-1, superior to those reported in the existing literature. In addition, CTT-POP-1 can be regenerated at least seven times with no loss in performance, indicating its potential application in water treatment. |
Author | Hu, Bing Cao, Xiao-Mei Hong, Xin Ding, San-Yuan Huang, Xiao-Qing Zhang, Yong Lin, Hui |
AuthorAffiliation | State Key Laboratory of Applied Organic Chemistry, College of Chemistry and Chemical Engineering Key Laboratory of Jiangxi Province for the Persistent Pollutants Control and Resources Recycle Nanchang Hangkong University Key Laboratory of Organo-Pharmaceutical Chemistry, College of Chemistry and Chemical Engineering |
AuthorAffiliation_xml | – name: Nanchang Hangkong University – name: Key Laboratory of Organo-Pharmaceutical Chemistry, College of Chemistry and Chemical Engineering – name: State Key Laboratory of Applied Organic Chemistry, College of Chemistry and Chemical Engineering – name: Key Laboratory of Jiangxi Province for the Persistent Pollutants Control and Resources Recycle |
Author_xml | – sequence: 1 givenname: Yong orcidid: 0000-0001-8911-4650 surname: Zhang fullname: Zhang, Yong email: yong_zhanggnnu@126.com organization: Key Laboratory of Organo-Pharmaceutical Chemistry, College of Chemistry and Chemical Engineering – sequence: 2 givenname: Xin surname: Hong fullname: Hong, Xin organization: Key Laboratory of Organo-Pharmaceutical Chemistry, College of Chemistry and Chemical Engineering – sequence: 3 givenname: Xiao-Mei surname: Cao fullname: Cao, Xiao-Mei organization: Key Laboratory of Organo-Pharmaceutical Chemistry, College of Chemistry and Chemical Engineering – sequence: 4 givenname: Xiao-Qing surname: Huang fullname: Huang, Xiao-Qing organization: Key Laboratory of Organo-Pharmaceutical Chemistry, College of Chemistry and Chemical Engineering – sequence: 5 givenname: Bing surname: Hu fullname: Hu, Bing organization: Key Laboratory of Organo-Pharmaceutical Chemistry, College of Chemistry and Chemical Engineering – sequence: 6 givenname: San-Yuan orcidid: 0000-0003-2160-4092 surname: Ding fullname: Ding, San-Yuan organization: State Key Laboratory of Applied Organic Chemistry, College of Chemistry and Chemical Engineering – sequence: 7 givenname: Hui surname: Lin fullname: Lin, Hui email: linhui07lanzhou@163.com organization: Nanchang Hangkong University |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/33517654$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.1126/science.1127291 10.1021/acsami.6b01754 10.1021/acsanm.9b02325 10.1039/d0cs00199f 10.1021/acsami.0c08817 10.1038/nature16185 10.1002/anie.201611542 10.1002/chem.201600162 10.1002/chem.201805713 10.1002/chem.201801765 10.1021/acs.macromol.8b00669 10.1021/ja206846p 10.1039/c6cs00851h 10.1021/acssuschemeng.8b04049 10.1021/acs.macromol.5b02222 10.1021/acsapm.8b00264 10.1126/science.aaa8075 10.1021/acssuschemeng.7b00031 10.1039/c9sc03725j 10.1039/c9cs00315k 10.1039/c6ta08388a 10.1002/chem.201705192 10.1039/c8cc04080j 10.1021/acs.chemrev.5b00361 10.1021/jacs.9b03463 10.1016/j.trechm.2019.02.010 10.1021/acsami.8b02566 10.1016/j.jclepro.2019.01.040 10.1016/s0032-9592(98)00112-5 10.1016/j.jhazmat.2007.07.079 10.1039/c9qm00633h 10.1021/jacs.5b10754 10.1021/acs.macromol.7b00971 10.1021/acs.chemrev.6b00439 10.1002/smll.201403729 10.1002/adfm.201907006 10.1021/cr300133d 10.1039/d0cc04784h 10.1002/anie.201602667 10.1039/c4ee01299b 10.1002/anie.201712816 10.1039/d0mh01317j 10.1021/jacs.9b02706 10.1021/acs.accounts.0c00007 10.1016/j.jcis.2009.04.071 10.1039/c8ta09145e 10.1002/anie.201500305 10.1039/c5ta03820k 10.1021/jp803903x 10.1021/acs.chemmater.9b02563 10.1002/adma.201900104 10.1021/acs.chemrev.9b00399 10.1021/jacs.7b02696 10.1039/c9cc09710d 10.1039/c9py01373c 10.1039/c6ta06656a 10.1016/j.jhazmat.2007.01.145 10.1021/acssuschemeng.8b01807 10.1021/acs.accounts.0c00426 10.1021/acsami.8b21674 10.1021/acsami.9b07874 10.1039/c7ta01255a 10.1021/ol201946f |
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Keywords | adsorption organic dyes conjugated triaryl triazine water treatment porous organic polymers |
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References | ref9/cit9 ref45/cit45 ref3/cit3 ref27/cit27 ref63/cit63 ref56/cit56 ref16/cit16 ref52/cit52 ref23/cit23 ref8/cit8 ref31/cit31 ref59/cit59 ref2/cit2 ref34/cit34 ref37/cit37 ref20/cit20 ref48/cit48 ref60/cit60 ref17/cit17 ref10/cit10 ref35/cit35 ref53/cit53 ref19/cit19 ref21/cit21 ref42/cit42 ref46/cit46 ref49/cit49 ref13/cit13 ref61/cit61 ref24/cit24 ref38/cit38 ref50/cit50 ref54/cit54 ref6/cit6 ref36/cit36 ref18/cit18 ref11/cit11 ref25/cit25 ref29/cit29 ref32/cit32 ref39/cit39 ref14/cit14 ref57/cit57 ref5/cit5 ref51/cit51 ref43/cit43 ref28/cit28 ref40/cit40 ref26/cit26 ref55/cit55 ref12/cit12 ref15/cit15 ref62/cit62 ref41/cit41 ref58/cit58 ref22/cit22 ref33/cit33 ref4/cit4 ref30/cit30 ref47/cit47 ref1/cit1 ref44/cit44 ref7/cit7 |
References_xml | – ident: ref1/cit1 doi: 10.1126/science.1127291 – ident: ref10/cit10 doi: 10.1021/acsami.6b01754 – ident: ref42/cit42 doi: 10.1021/acsanm.9b02325 – ident: ref19/cit19 doi: 10.1039/d0cs00199f – ident: ref22/cit22 doi: 10.1021/acsami.0c08817 – ident: ref25/cit25 doi: 10.1038/nature16185 – ident: ref47/cit47 doi: 10.1002/anie.201611542 – ident: ref11/cit11 doi: 10.1002/chem.201600162 – ident: ref48/cit48 doi: 10.1002/chem.201805713 – ident: ref36/cit36 doi: 10.1002/chem.201801765 – ident: ref5/cit5 doi: 10.1021/acs.macromol.8b00669 – ident: ref21/cit21 doi: 10.1021/ja206846p – ident: ref13/cit13 doi: 10.1039/c6cs00851h – ident: ref34/cit34 doi: 10.1021/acssuschemeng.8b04049 – ident: ref28/cit28 doi: 10.1021/acs.macromol.5b02222 – ident: ref59/cit59 doi: 10.1021/acsapm.8b00264 – ident: ref12/cit12 doi: 10.1126/science.aaa8075 – ident: ref40/cit40 doi: 10.1021/acssuschemeng.7b00031 – ident: ref2/cit2 doi: 10.1039/c9sc03725j – ident: ref15/cit15 doi: 10.1039/c9cs00315k – ident: ref30/cit30 doi: 10.1039/c6ta08388a – ident: ref33/cit33 doi: 10.1002/chem.201705192 – ident: ref49/cit49 doi: 10.1039/c8cc04080j – ident: ref6/cit6 doi: 10.1021/acs.chemrev.5b00361 – ident: ref17/cit17 doi: 10.1021/jacs.9b03463 – ident: ref18/cit18 doi: 10.1016/j.trechm.2019.02.010 – ident: ref35/cit35 doi: 10.1021/acsami.8b02566 – ident: ref46/cit46 doi: 10.1016/j.jclepro.2019.01.040 – ident: ref62/cit62 doi: 10.1016/s0032-9592(98)00112-5 – ident: ref9/cit9 doi: 10.1016/j.jhazmat.2007.07.079 – ident: ref23/cit23 doi: 10.1039/c9qm00633h – ident: ref24/cit24 doi: 10.1021/jacs.5b10754 – ident: ref29/cit29 doi: 10.1021/acs.macromol.7b00971 – ident: ref14/cit14 doi: 10.1021/acs.chemrev.6b00439 – ident: ref8/cit8 doi: 10.1002/smll.201403729 – ident: ref20/cit20 doi: 10.1002/adfm.201907006 – ident: ref7/cit7 doi: 10.1021/cr300133d – ident: ref43/cit43 doi: 10.1039/d0cc04784h – ident: ref57/cit57 doi: 10.1002/anie.201602667 – ident: ref3/cit3 doi: 10.1039/c4ee01299b – ident: ref51/cit51 doi: 10.1002/anie.201712816 – ident: ref55/cit55 doi: 10.1039/d0mh01317j – ident: ref53/cit53 doi: 10.1021/jacs.9b02706 – ident: ref26/cit26 doi: 10.1021/acs.accounts.0c00007 – ident: ref63/cit63 doi: 10.1016/j.jcis.2009.04.071 – ident: ref37/cit37 doi: 10.1039/c8ta09145e – ident: ref56/cit56 doi: 10.1002/anie.201500305 – ident: ref4/cit4 doi: 10.1039/c5ta03820k – ident: ref60/cit60 doi: 10.1021/jp803903x – ident: ref44/cit44 doi: 10.1021/acs.chemmater.9b02563 – ident: ref52/cit52 doi: 10.1002/adma.201900104 – ident: ref16/cit16 doi: 10.1021/acs.chemrev.9b00399 – ident: ref50/cit50 doi: 10.1021/jacs.7b02696 – ident: ref58/cit58 doi: 10.1039/c9cc09710d – ident: ref45/cit45 doi: 10.1039/c9py01373c – ident: ref31/cit31 doi: 10.1039/c6ta06656a – ident: ref61/cit61 doi: 10.1016/j.jhazmat.2007.01.145 – ident: ref39/cit39 doi: 10.1021/acssuschemeng.8b01807 – ident: ref27/cit27 doi: 10.1021/acs.accounts.0c00426 – ident: ref38/cit38 doi: 10.1021/acsami.8b21674 – ident: ref41/cit41 doi: 10.1021/acsami.9b07874 – ident: ref32/cit32 doi: 10.1039/c7ta01255a – ident: ref54/cit54 doi: 10.1021/ol201946f |
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Snippet | Developing efficient adsorbents for the removal of water pollutants is of great significance for environmental protection. In this study, conjugated triaryl... |
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SubjectTerms | adsorbents adsorption Energy, Environmental, and Catalysis Applications hydrogen bonding methylene blue polymers triazines water treatment wettability |
Title | Functional Porous Organic Polymers with Conjugated Triaryl Triazine as the Core for Superfast Adsorption Removal of Organic Dyes |
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