2019
DOI: 10.3390/polym11010059
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Preparation of Porous Polymeric Membranes Based on a Pyridine Containing Aromatic Polyether Sulfone

Abstract: Polymeric membranes, based on a polysulfone-type aromatic polyether matrix, were successfully developed via the non-solvent induced phase separation (NIPS) method. The polyethersulfone type polymer poly[2-(4-(diphenylsulfonyl)-phenoxy)-6-(4-phenoxy) pyridine] (PDSPP) was used as the membrane matrix, and mixed with its sulfonated derivative (SPDSPP) and a polymeric porogen. The SPDPPP was added to impart hydrophilicity, while at the same time maintaining the interactions with the non-sulfonated aromatic polyeth… Show more

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Cited by 41 publications
(17 citation statements)
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“…At first, as shown in Scheme 2 —route a, a “post-polymerization” complexation approach was selected. In this, the diphenyl pyridine moieties of the homopolymer ( pySO 2 ) [ 48 ], prepared from 2,6-dihydroxyphenylpyridine ( HOpy ) [ 47 ] and difluorophenylsulfone ( diFSO 2 ), were complexated with the terpyridine-Ir monocomplexes with dodecyloxy or methyl side groups, C 12 Otpy-IrCl 3 and CH 3 tpy-IrCl 3 , respectively. Various percentages of complexation were investigated to transfer the photophysical properties of the monomeric complexes to the copolymeric metallocomplexes.…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…At first, as shown in Scheme 2 —route a, a “post-polymerization” complexation approach was selected. In this, the diphenyl pyridine moieties of the homopolymer ( pySO 2 ) [ 48 ], prepared from 2,6-dihydroxyphenylpyridine ( HOpy ) [ 47 ] and difluorophenylsulfone ( diFSO 2 ), were complexated with the terpyridine-Ir monocomplexes with dodecyloxy or methyl side groups, C 12 Otpy-IrCl 3 and CH 3 tpy-IrCl 3 , respectively. Various percentages of complexation were investigated to transfer the photophysical properties of the monomeric complexes to the copolymeric metallocomplexes.…”
Section: Resultsmentioning
confidence: 99%
“…4(Phenyl-4-hydroxy) terpyridine ( HOtpy ) [ 46 ], 4 (phenyl-4-dodecyloxy) terpyridine ( C 12 Otpy ) [ 46 ], 2,6-Bis(4-hydroxyphenyl)pyridine ( HOpy ) [ 47 ], and the homopolymer ( pySO 2 ) [ 48 ] were prepared according to literature procedures. Bis(4-fluorophenyl)sulfone ( diFSO 2 ) was purchased from Chemos GmbH (Altdorf, Germany).…”
Section: Methodsmentioning
confidence: 99%
“…The porosity of the substrate was determined using dry-wet weight technique. 41 The porosity (%) was measured as a function of the weight of membrane.…”
Section: Evaluation Of Performance Of Substrate and Tfc/tfn Membranesmentioning
confidence: 99%
“…There is no economic justification for the former method, especially as the concentration of natural organic matter in raw water increases, whereas regarding the latter – advanced oxidation processes – the main challenge is the possibility of forming undesirable byproducts that represent an increase in antagonistic effects such as toxicity and estrogenic activity 2,3 . Yet, one set of established and mature technologies that has demonstrated sustainability and pollution control attributes in a variety of environmental, biological and food processing applications involves the exploitation of membrane technology; most notably pressure‐driven, polymeric membrane processes, due to the low cost of production and ease of operation, seem to be a good solution for overcoming this global challenge 9–12 . One exceptional feature of membranes that has enhanced their potential to replace conventional treatment processes is that they can be used in independent processes or be a part of integrated/hybrid systems with other conventional separation technologies such as coagulation or sorption on active carbon and membrane bioreactors 4,13–19 …”
Section: Introductionmentioning
confidence: 99%