Reactable substrate participating interfacial polymerization for thin film composite membranes with enhanced salt rejection performance

Desalination ◽  
2018 ◽  
Vol 436 ◽  
pp. 1-7 ◽  
Author(s):  
Zhikan Yao ◽  
Hao Guo ◽  
Zhe Yang ◽  
Chuner Lin ◽  
Baoku Zhu ◽  
...  
RSC Advances ◽  
2015 ◽  
Vol 5 (96) ◽  
pp. 78950-78957 ◽  
Author(s):  
Pravin G. Ingole ◽  
Won Kil Choi ◽  
Il-Hyun Baek ◽  
Hyung Keun Lee

In the present study, thin film composite membranes have been prepared using an interfacial polymerization method.


2021 ◽  
Author(s):  
Lorena Paseta ◽  
Carlos Echaide-Gorriz ◽  
Carlos Téllez Ariso ◽  
Joaquin Coronas

Thin film composite membranes (TFC) of polyamide (PA) prepared by interfacial polymerization (IP) between a diamine and an acyl chloride are those applied to industrial nanofiltration and reverse osmosis. Water,...


Membranes ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 297
Author(s):  
Peter-Renaat Van den Mooter ◽  
Liridona Dedvukaj ◽  
Ivo F. J. Vankelecom

Polyamide (PA) thin-film composite (TFC) membranes are commonly applied in reversed osmosis (RO) and nanofiltration (NF) applications due to their thin, dense top-layer, and high selectivity. Recently, the conventional organic phase (i.e., hexane) during interfacial polymerization (IP) was replaced by less toxic ionic liquids (ILs) which led to excellent membrane performances. As the high price of most ILs limits their up-scaling, the potential use of inexpensive Aliquat was investigated in this study. The thin-film composite (TFC) membranes were optimized to remove flavor compounds, i.e., ethyl acetate (EA) and isoamyl acetate (IA), from a fermentation broth. A multi-parameter optimization was set-up involving type of support, reaction time for IP, water content of Aliquat, and concentration of both monomers m-phenylenediamine (MPD) and trimesoylchloride (TMC). The membranes prepared using Aliquat showed similar fluxes as those prepared from a reference IL 1-butyl-1-methylpyrrolidinium bis(trifluoromethylsulfonyl)imide ([C4mpyr][Tf2N]) but with better EA and IA retentions, even better than for a commercial RO membrane (GEA type AF). Finally, the recently introduced epoxide-curing of Bisphenol A diglycidyl ether (BADGE) with 1,6-hexanediamine (HDA) was investigated using Aliquat as organic phase. It is the first time this type of IP was performed in combination with an IL as organic phase. The resulting membrane was used in the filtration of a 35 µM Rose Bengal (RB) in 20 wt% dimethylformamide/ water (DMF/H2O) feed mixture. A well-crosslinked poly(β-alkanolamine) film was obtained with a > 97% retention.


Desalination ◽  
2022 ◽  
Vol 524 ◽  
pp. 115481
Author(s):  
Ruth Habte Hailemariam ◽  
June-Seok Choi ◽  
Mekdimu Mezemir Damtie ◽  
Hojung Rho ◽  
Kwang-Duck Park ◽  
...  

2013 ◽  
Vol 377 ◽  
pp. 222-226 ◽  
Author(s):  
Shu Hsien Huang ◽  
Chuan Hsiang Wu ◽  
Kueir Rarn Lee ◽  
Juin Yih Lai

To dehydrate the isopropanol (IPA) by the pervaporation separation process at 25°C, the polysulfonamide thin-film composite (TFC) membranes were prepared via the interfacial polymerization of diamines including 1,3-diaminopropane (DAPE), 1,3-cyclohexanediamine (CHDA) and m-phenylenediamine (MPDA) with 1,3-benzenedisulfonyl dichloride (BDSC) on the surface of modified asymmetric polyacrylonitrile (mPAN) membrane. Attenuated Total Reflectance-Fourier Transform Infrared (ATR-FTIR) Spectrometry, atomic force microscope (AFM) and water contact angle (WCA) measurements were applied to analyze chemical structure, surface roughness and hydrophilicity of the polymerized layer of composite membrane. In the dehydration of aqueous isopropanol solutions, the DAPE-BDSC/mPAN membrane had the higher permeation flux and the similar water concentration in permeate compared with the CHDA-BDSC/mPAN and MPDA-BDSC/mPAN membranes. The pervaporation performance of the composite membrane was affected by the chemical structure of the polysulfonamide polymer.


2010 ◽  
Vol 362 (1-2) ◽  
pp. 265-278 ◽  
Author(s):  
Xingwei Yu ◽  
Zhi Wang ◽  
Zhihong Wei ◽  
Shuangjie Yuan ◽  
Juan Zhao ◽  
...  

2017 ◽  
Vol 10 (1) ◽  
Author(s):  
B. J. Abu Tarboush ◽  
H. A. Arafat ◽  
T. Matsuura ◽  
D. Rana

Reverse osmosis (RO) by polymeric membranes is known to be among the successful technologies for brackish and seawater desalination. For the development of these polymeric RO membranes, two different techniques have been used – the phase inversion method for asymmetric membranes, such as cellulose acetate membrane and the interfacial polymerization for thin film composite (TFC) membranes. Despite the high quality of the water produced by TFC–RO process, TFC membranes are susceptible to fouling. After a long period of academic and industrial researches, it is generally accepted that hydrophilicity, surface charge, and surface roughness of the TFC membrane surface are the major factors which affect the membrane susceptibility to fouling. As a result, several recent studies have focused on tailoring these properties with the aim of producing TFC membranes with reduced fouling as well as enhanced flux and salt rejection for use in desalination.In this study, authors present a comprehensive summary of the most recent findings in the literature focusing on the enhancement of TFC RO and nanofiltration membrane performance in desalination applications, by tailoring membrane characteristics. The authors would then present a new concept for the preparation of TFC membranes by interfacial polymerization on porous polysulfone support using novel additives, namely, surface modifying macromolecules (SMMs). Hydrophilic SMMs (LSMMs) were synthesized both ex–situ and in–situ within the organic solvent of the TFC system. The RO performance results showed that the addition of the ex–situ LSMM significantly decreased the salt rejection of the membrane and slightly reduced the flux, while in the case of the in–situ LSMM, salt rejection was improved but the flux declined at different rates for different LSMM concentrations. The membrane prepared by the in–situ LSMM exhibited less flux decay over an extended operational period.


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