Cargando…

Optimal Performance of Thin-Film Composite Nanofiltration-Like Forward Osmosis Membranes Set Off by Changing the Chemical Structure of Diamine Reacted with Trimesoyl Chloride through Interfacial Polymerization

Thin-film composite (TFC) polyamide membranes formed through interfacial polymerization can function more efficiently by tuning the chemical structure of participating monomers. Accordingly, three kinds of diamine monomers were considered to take part in interfacial polymerization. Each diamine was...

Descripción completa

Detalles Bibliográficos
Autores principales: De Guzman, Manuel Reyes, Ang, Micah Belle Marie Yap, Huang, Shu-Hsien, Huang, Qing-Yi, Chiao, Yu-Hsuan, Lee, Kueir-Rarn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7918250/
https://www.ncbi.nlm.nih.gov/pubmed/33673191
http://dx.doi.org/10.3390/polym13040544
_version_ 1783657883286634496
author De Guzman, Manuel Reyes
Ang, Micah Belle Marie Yap
Huang, Shu-Hsien
Huang, Qing-Yi
Chiao, Yu-Hsuan
Lee, Kueir-Rarn
author_facet De Guzman, Manuel Reyes
Ang, Micah Belle Marie Yap
Huang, Shu-Hsien
Huang, Qing-Yi
Chiao, Yu-Hsuan
Lee, Kueir-Rarn
author_sort De Guzman, Manuel Reyes
collection PubMed
description Thin-film composite (TFC) polyamide membranes formed through interfacial polymerization can function more efficiently by tuning the chemical structure of participating monomers. Accordingly, three kinds of diamine monomers were considered to take part in interfacial polymerization. Each diamine was reacted with trimesoyl chloride (TMC) to manufacture TFC polyamide nanofiltration (NF)-like forward osmosis (FO) membranes. The diamines differed in chemical structure; the functional group present between the terminal amines was classified as follows: aliphatic group of 1,3-diaminopropane (DAPE); cyclohexane in 1,3-cyclohexanediamine (CHDA); and aromatic or benzene ring in m-phenylenediamine (MPD). For FO tests, deionized water and 1 M aqueous sodium sulfate solution were used as feed and draw solution, respectively. Interfacial polymerization conditions were also varied: concentrations of water and oil phases, time of contact between the water-phase solution and the membrane substrate, and polymerization reaction time. The resultant membranes were characterized using attenuated total reflectance-Fourier transform infrared spectroscopy, field emission scanning electron microscopy, atomic force microscopy, and surface contact angle measurement to identify the chemical structure, morphology, roughness, and hydrophilicity of the polyamide layer, respectively. The results of FO experiments revealed that among the three diamine monomers, CHDA turned out to be the most effective, as it led to the production of TFC NF-like FO membrane with optimal performance. Then, the following optimum conditions were established for the CHDA-based membrane: contact between 2.5 wt.% aqueous CHDA solution and polysulfone (PSf) substrate for 2 min, and polymerization reaction between 1 wt.% TMC solution and 2.5 wt.% CHDA solution for 30 s. The composite CHDA-TMC/PSf membrane delivered a water flux (Jw) of 18.24 ± 1.33 LMH and a reverse salt flux (Js) of 5.75 ± 1.12 gMH; therefore, Js/Jw was evaluated to be 0.32 ± 0.07 (g/L).
format Online
Article
Text
id pubmed-7918250
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-79182502021-03-02 Optimal Performance of Thin-Film Composite Nanofiltration-Like Forward Osmosis Membranes Set Off by Changing the Chemical Structure of Diamine Reacted with Trimesoyl Chloride through Interfacial Polymerization De Guzman, Manuel Reyes Ang, Micah Belle Marie Yap Huang, Shu-Hsien Huang, Qing-Yi Chiao, Yu-Hsuan Lee, Kueir-Rarn Polymers (Basel) Article Thin-film composite (TFC) polyamide membranes formed through interfacial polymerization can function more efficiently by tuning the chemical structure of participating monomers. Accordingly, three kinds of diamine monomers were considered to take part in interfacial polymerization. Each diamine was reacted with trimesoyl chloride (TMC) to manufacture TFC polyamide nanofiltration (NF)-like forward osmosis (FO) membranes. The diamines differed in chemical structure; the functional group present between the terminal amines was classified as follows: aliphatic group of 1,3-diaminopropane (DAPE); cyclohexane in 1,3-cyclohexanediamine (CHDA); and aromatic or benzene ring in m-phenylenediamine (MPD). For FO tests, deionized water and 1 M aqueous sodium sulfate solution were used as feed and draw solution, respectively. Interfacial polymerization conditions were also varied: concentrations of water and oil phases, time of contact between the water-phase solution and the membrane substrate, and polymerization reaction time. The resultant membranes were characterized using attenuated total reflectance-Fourier transform infrared spectroscopy, field emission scanning electron microscopy, atomic force microscopy, and surface contact angle measurement to identify the chemical structure, morphology, roughness, and hydrophilicity of the polyamide layer, respectively. The results of FO experiments revealed that among the three diamine monomers, CHDA turned out to be the most effective, as it led to the production of TFC NF-like FO membrane with optimal performance. Then, the following optimum conditions were established for the CHDA-based membrane: contact between 2.5 wt.% aqueous CHDA solution and polysulfone (PSf) substrate for 2 min, and polymerization reaction between 1 wt.% TMC solution and 2.5 wt.% CHDA solution for 30 s. The composite CHDA-TMC/PSf membrane delivered a water flux (Jw) of 18.24 ± 1.33 LMH and a reverse salt flux (Js) of 5.75 ± 1.12 gMH; therefore, Js/Jw was evaluated to be 0.32 ± 0.07 (g/L). MDPI 2021-02-12 /pmc/articles/PMC7918250/ /pubmed/33673191 http://dx.doi.org/10.3390/polym13040544 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
De Guzman, Manuel Reyes
Ang, Micah Belle Marie Yap
Huang, Shu-Hsien
Huang, Qing-Yi
Chiao, Yu-Hsuan
Lee, Kueir-Rarn
Optimal Performance of Thin-Film Composite Nanofiltration-Like Forward Osmosis Membranes Set Off by Changing the Chemical Structure of Diamine Reacted with Trimesoyl Chloride through Interfacial Polymerization
title Optimal Performance of Thin-Film Composite Nanofiltration-Like Forward Osmosis Membranes Set Off by Changing the Chemical Structure of Diamine Reacted with Trimesoyl Chloride through Interfacial Polymerization
title_full Optimal Performance of Thin-Film Composite Nanofiltration-Like Forward Osmosis Membranes Set Off by Changing the Chemical Structure of Diamine Reacted with Trimesoyl Chloride through Interfacial Polymerization
title_fullStr Optimal Performance of Thin-Film Composite Nanofiltration-Like Forward Osmosis Membranes Set Off by Changing the Chemical Structure of Diamine Reacted with Trimesoyl Chloride through Interfacial Polymerization
title_full_unstemmed Optimal Performance of Thin-Film Composite Nanofiltration-Like Forward Osmosis Membranes Set Off by Changing the Chemical Structure of Diamine Reacted with Trimesoyl Chloride through Interfacial Polymerization
title_short Optimal Performance of Thin-Film Composite Nanofiltration-Like Forward Osmosis Membranes Set Off by Changing the Chemical Structure of Diamine Reacted with Trimesoyl Chloride through Interfacial Polymerization
title_sort optimal performance of thin-film composite nanofiltration-like forward osmosis membranes set off by changing the chemical structure of diamine reacted with trimesoyl chloride through interfacial polymerization
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7918250/
https://www.ncbi.nlm.nih.gov/pubmed/33673191
http://dx.doi.org/10.3390/polym13040544
work_keys_str_mv AT deguzmanmanuelreyes optimalperformanceofthinfilmcompositenanofiltrationlikeforwardosmosismembranessetoffbychangingthechemicalstructureofdiaminereactedwithtrimesoylchloridethroughinterfacialpolymerization
AT angmicahbellemarieyap optimalperformanceofthinfilmcompositenanofiltrationlikeforwardosmosismembranessetoffbychangingthechemicalstructureofdiaminereactedwithtrimesoylchloridethroughinterfacialpolymerization
AT huangshuhsien optimalperformanceofthinfilmcompositenanofiltrationlikeforwardosmosismembranessetoffbychangingthechemicalstructureofdiaminereactedwithtrimesoylchloridethroughinterfacialpolymerization
AT huangqingyi optimalperformanceofthinfilmcompositenanofiltrationlikeforwardosmosismembranessetoffbychangingthechemicalstructureofdiaminereactedwithtrimesoylchloridethroughinterfacialpolymerization
AT chiaoyuhsuan optimalperformanceofthinfilmcompositenanofiltrationlikeforwardosmosismembranessetoffbychangingthechemicalstructureofdiaminereactedwithtrimesoylchloridethroughinterfacialpolymerization
AT leekueirrarn optimalperformanceofthinfilmcompositenanofiltrationlikeforwardosmosismembranessetoffbychangingthechemicalstructureofdiaminereactedwithtrimesoylchloridethroughinterfacialpolymerization