Charge tunable thin-film composite membranes by gamma-ray triggered surface polymerization
Abstract Thin-film composite poly(amide) (PA) membranes have greatly diversified water supplies and food products. However, users would benefit from a control of the electrostatic interactions between the liquid and the net surface charge interface in order to benefit wider application. The ionic se...
Guardado en:
Autores principales: | , , , , , , |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Nature Portfolio
2017
|
Materias: | |
Acceso en línea: | https://doaj.org/article/e20ba6c793054aa18bb5c228aea42a6b |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
id |
oai:doaj.org-article:e20ba6c793054aa18bb5c228aea42a6b |
---|---|
record_format |
dspace |
spelling |
oai:doaj.org-article:e20ba6c793054aa18bb5c228aea42a6b2021-12-02T16:07:06ZCharge tunable thin-film composite membranes by gamma-ray triggered surface polymerization10.1038/s41598-017-04900-52045-2322https://doaj.org/article/e20ba6c793054aa18bb5c228aea42a6b2017-06-01T00:00:00Zhttps://doi.org/10.1038/s41598-017-04900-5https://doaj.org/toc/2045-2322Abstract Thin-film composite poly(amide) (PA) membranes have greatly diversified water supplies and food products. However, users would benefit from a control of the electrostatic interactions between the liquid and the net surface charge interface in order to benefit wider application. The ionic selectivity of the 100 nm PA semi-permeable layer is significantly affected by the pH of the solution. In this work, for the first time, a convenient route is presented to configure the surface charge of PA membranes by gamma ray induced surface grafting. This rapid and up-scalable method offers a versatile route for surface grafting by adjusting the irradiation total dose and the monomer concentration. Specifically, thin coatings obtained at low irradiation doses between 1 and 10 kGy and at low monomer concentration of 1 v/v% in methanol/water (1:1) solutions, dramatically altered the net surface charge of the pristine membranes from −25 mV to +45 mV, whilst the isoelectric point of the materials shifted from pH 3 to pH 7. This modification resulted in an improved water flux by over 55%, from 45.9 to up 70 L.m−2.h−1, whilst NaCl rejection was found to drop by only 1% compared to pristine membranes.Rackel ReisMikel C. DukeBlaise L. TardyDaniel OldfieldRaymond R. DagastineJohn D. OrbellLudovic F. DuméeNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 7, Iss 1, Pp 1-10 (2017) |
institution |
DOAJ |
collection |
DOAJ |
language |
EN |
topic |
Medicine R Science Q |
spellingShingle |
Medicine R Science Q Rackel Reis Mikel C. Duke Blaise L. Tardy Daniel Oldfield Raymond R. Dagastine John D. Orbell Ludovic F. Dumée Charge tunable thin-film composite membranes by gamma-ray triggered surface polymerization |
description |
Abstract Thin-film composite poly(amide) (PA) membranes have greatly diversified water supplies and food products. However, users would benefit from a control of the electrostatic interactions between the liquid and the net surface charge interface in order to benefit wider application. The ionic selectivity of the 100 nm PA semi-permeable layer is significantly affected by the pH of the solution. In this work, for the first time, a convenient route is presented to configure the surface charge of PA membranes by gamma ray induced surface grafting. This rapid and up-scalable method offers a versatile route for surface grafting by adjusting the irradiation total dose and the monomer concentration. Specifically, thin coatings obtained at low irradiation doses between 1 and 10 kGy and at low monomer concentration of 1 v/v% in methanol/water (1:1) solutions, dramatically altered the net surface charge of the pristine membranes from −25 mV to +45 mV, whilst the isoelectric point of the materials shifted from pH 3 to pH 7. This modification resulted in an improved water flux by over 55%, from 45.9 to up 70 L.m−2.h−1, whilst NaCl rejection was found to drop by only 1% compared to pristine membranes. |
format |
article |
author |
Rackel Reis Mikel C. Duke Blaise L. Tardy Daniel Oldfield Raymond R. Dagastine John D. Orbell Ludovic F. Dumée |
author_facet |
Rackel Reis Mikel C. Duke Blaise L. Tardy Daniel Oldfield Raymond R. Dagastine John D. Orbell Ludovic F. Dumée |
author_sort |
Rackel Reis |
title |
Charge tunable thin-film composite membranes by gamma-ray triggered surface polymerization |
title_short |
Charge tunable thin-film composite membranes by gamma-ray triggered surface polymerization |
title_full |
Charge tunable thin-film composite membranes by gamma-ray triggered surface polymerization |
title_fullStr |
Charge tunable thin-film composite membranes by gamma-ray triggered surface polymerization |
title_full_unstemmed |
Charge tunable thin-film composite membranes by gamma-ray triggered surface polymerization |
title_sort |
charge tunable thin-film composite membranes by gamma-ray triggered surface polymerization |
publisher |
Nature Portfolio |
publishDate |
2017 |
url |
https://doaj.org/article/e20ba6c793054aa18bb5c228aea42a6b |
work_keys_str_mv |
AT rackelreis chargetunablethinfilmcompositemembranesbygammaraytriggeredsurfacepolymerization AT mikelcduke chargetunablethinfilmcompositemembranesbygammaraytriggeredsurfacepolymerization AT blaiseltardy chargetunablethinfilmcompositemembranesbygammaraytriggeredsurfacepolymerization AT danieloldfield chargetunablethinfilmcompositemembranesbygammaraytriggeredsurfacepolymerization AT raymondrdagastine chargetunablethinfilmcompositemembranesbygammaraytriggeredsurfacepolymerization AT johndorbell chargetunablethinfilmcompositemembranesbygammaraytriggeredsurfacepolymerization AT ludovicfdumee chargetunablethinfilmcompositemembranesbygammaraytriggeredsurfacepolymerization |
_version_ |
1718384750911029248 |