Polyester Thin Film Composite Nanofiltration Membranes Prepared by Interfacial Polymerization Technique for Removal of Humic Acid

Author(s):  
M. N. Abu Seman ◽  
N. A. Jalanni ◽  
C. K. M. Faizal ◽  
N. Hilal
2020 ◽  
Vol 8 (6) ◽  
pp. 3238-3245 ◽  
Author(s):  
Shushan Yuan ◽  
Gang Zhang ◽  
Junyong Zhu ◽  
Natalie Mamrol ◽  
Suilin Liu ◽  
...  

This study demonstrates the application of a hydrogel as the aqueous phase in interfacial polymerization for the synthesis of a thin film composite membrane with ultrahigh permeability.


Polymers ◽  
2020 ◽  
Vol 12 (2) ◽  
pp. 269 ◽  
Author(s):  
Yu-Hsuan Chiao ◽  
Tanmoy Patra ◽  
Micah Belle Marie Yap Ang ◽  
Shu-Ting Chen ◽  
Jorge Almodovar ◽  
...  

Nanofiltration membranes have evolved as a promising solution to tackle the clean water scarcity and wastewater treatment processes with their low energy requirement and environment friendly operating conditions. Thin film composite nanofiltration membranes with high permeability, and excellent antifouling and antibacterial properties are important component for wastewater treatment and clean drinking water production units. In the scope of this study, thin film composite nanofiltration membranes were fabricated using polyacrylonitrile (PAN) support and fast second interfacial polymerization modification methods by grafting polyethylene amine and zwitterionic sulfobutane methacrylate moieties. Chemical and physical alteration in structure of the membranes were characterized using methods like ATR-FTIR spectroscopy, XPS analysis, FESEM and AFM imaging. The effects of second interfacial polymerization to incorporate polyamide layer and ‘ion pair’ characteristics, in terms of water contact angle and surface charge analysis was investigated in correlation with nanofiltration performance. Furthermore, the membrane characteristics in terms of antifouling properties were evaluated using model protein foulants like bovine serum albumin and lysozyme. Antibacterial properties of the modified membranes were investigated using E. coli as model biofoulant. Overall, the effect of second interfacial polymerization without affecting the selectivity layer of nanofiltration membrane for their potential large-scale application was investigated in detail.


Nanomaterials ◽  
2021 ◽  
Vol 11 (10) ◽  
pp. 2470
Author(s):  
Yingfu Lian ◽  
Gang Zhang ◽  
Xiaojun Wang ◽  
Jie Yang

Our current study experimentally evaluates the impacts of surface hydrophilicity of supports on the properties of polyamide (PA) thin-film composite (TFC) nanofiltration (NF) membranes. A series of “carboxylated polyethersulfone” (CPES) copolymers with an increasing “molar ratio” (MR) of carboxyl units were used to prepare supports with diverse surface hydrophilicities by the classical nonsolvent-induced phase separation (NIPS) method. Then, the PA-TFC NF membranes were finely fabricated atop these supports by conventional interfacial polymerization (IP) reactions. The linkages between the surface hydrophilicity of the supports and the characteristics of the interfacially polymerized PA layers as well as the permselectivity of NF membranes were investigated systematically. The morphological details of the NF membranes indicate that the growth of PA layers can be adjusted through increasing the surface hydrophilicity of the supports. Moreover, the separation results reveal that the NF membrane fabricated on the relatively hydrophobic support exhibits lower permeability (7.04 L·m−2·h−1·bar−1) and higher selectivity (89.94%) than those of the ones prepared on the hydrophilic supports (14.64~18.99 L·m−2·h−1·bar−1 and 66.98~73.48%). A three-stage conceptual scenario is proposed to illustrate the formation mechanism of the PA layer in NF membranes, which is due to the variation of surface hydrophilicity of the supports. The overall findings specify how the surface hydrophilicity of the supports influences the formation of PA layers, which ultimately defines the separation performances of the corresponding NF membranes.


2016 ◽  
Vol 78 (12) ◽  
Author(s):  
K. H. Mah ◽  
H. W. Yussof ◽  
M. N. Abu Seman ◽  
A. W. Mohammad

Polyester thin film composite nanofiltration membranes were synthesized on the polyethersulfone (PES) support via the interfacial polymerization between triethanolamine (TEOA) and trimesoyl chloride (TMC). Here we report the effect of curing time in the interfacial polymerization process on membrane properties like pore size and effective thickness/porosity. The membrane properties were determined based on the uncharged solute permeation test and the hypothetical mechanistic structure (pore size, effective thickness/porosity) was determined using Donnan steric pore flow model (DSPM). This study also provides information on the effect of curing time on water permeability. From the 2 minute point to 10 minute point, the membranes pore sizes were reduced and negligible changes to effective thickness/porosity suggest the occurrence of additional cross-linking reaction between aqueous and organic monomers.


RSC Advances ◽  
2017 ◽  
Vol 7 (68) ◽  
pp. 42800-42810 ◽  
Author(s):  
Shanshan Yang ◽  
Hongyan Zhen ◽  
Baowei Su

High performance solvent resistant nanofiltration membranes are fabricated via interfacial polymerization between m-phenylenediamine and 1,2,4,5-benzenetetra acylchloride on hydrolyzed polyacrylonitrile supports followed by chemical imidization.


2017 ◽  
Vol 79 (1-2) ◽  
Author(s):  
Mohammad Amirul Mohd Yusof ◽  
Mazrul Nizam Abu Seman

Nowadays, wide applications of forward osmosis (FO) technology have been huge attention in solving the water shortage problems. Hence, the performance of thin film composite (TFC) forward osmosis membrane via interfacial polymerization (IP) was studied. 2% and 1% w/v of piperazine (PIP) and 0.15% w/v of trimesoyl chloride (TMC) were reacted with 3 different reaction time (60s, 30s, and 10s). The fabricated membranes were then characterized by FTIR, contact angle measurement and FESEM. Pure water flux, humic acid rejection (represent NOM) and salt leakage were evaluated to obtain the best polyamide FO membrane. The results demonstrated that polyamide FO membranes fabricated with 2% w/v possess a higher hydrophilic properties compared to 1% w/v. In addition, regardless of monomer concentrations, at longest reaction time (60s), there is no significant change in water flux. Membrane fabricated at 60s of reaction time exhibited water flux of 1.90 LMH and 1.92 LMH for 2% w/v and 1% w/v of PIP concentrations, respectively. The same trend also observed for humic acid rejection (93.9%-94.6%). The salt leakage test revealed that the minimum salt reverse diffusion (0.01-0.02 GMH) could be achieved for membrane fabricated at longest reaction time of 60s for both PIP concentrations. As conclusion, manipulating monomer concentrations and reaction time is the main key to obtain an optimal polyamide layer with high membrane performance covering higher water flux, higher removal of humic acid and lower reverse salt diffusion.  


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