Abstract

A novel kind of pH-stable positively charged composite nanofiltration (NF) membrane with excellent rejection performance was developed via interfacial polymerization on the surface of a polysulfone (PSF) ultrafiltration (UF) membrane, using a mixture of polyethyleneimine (PEI) and piperazine (PIP) as the monomers of the aqueous phase, and cyanuric chloride (CC) as the monomer of the organic phase. The strong electron withdrawing and steric hindrance effects of the chloride group in the molecules of CC could protect the amido bond from the attack of hydrogen ions (H+) or hydroxyl ions (OH−) under acidic or alkaline conditions, thus the resultant polyamide composite membranes could be stable in acidic or alkali aqueous solution. A more compact PA active layer could be developed via mixing PIP into the PEI aqueous solution, where the PIP molecules could fill the pores of the polymer networks. There was no obvious change in the surface morphologies, the chemical structures, and the rejection performances after immersing the resultant polyamine composite NF membranes in the strong acidic solution (pH 1) and the strong alkaline solution (pH 13) for 30 days, respectively. The rejection performances of this kind of polyamine composite NF membranes could be adjusted through adjusting the mass ratio of PEI to PIP in the aqueous phase.

Highlights

  • Nano ltration (NF) has been widely applied to the separation of low-molecular weight organic matter and multi-/divalent ions from monovalent ions, including in wastewater treatment, desalination, water so ening and puri cation, the pharmaceutical and dye industries, etc.[1]

  • The rejection performances of PEI composite NF membranes could be enhanced by doping the amine monomer with low molecular weight in the PEI aqueous phase, such as piperazine (PIP), to obtain a more compact active layer

  • The PEI/PIP-cyanuric chloride (CC)/PSF composite NF membrane was constituted by two different active layers

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Summary

Introduction

On the surface of the PA selective layer to prevent the attacking from H+ or OHÀ. According to the mechanism of PA at acidic or alkaline condition, it could be inferred that electron-donating groups and electron-withdrawing groups could prevent the amide bond from the attacking of H+ or OHÀ, respectively. The rejection performances of PEI composite NF membranes could be enhanced by doping the amine monomer with low molecular weight in the PEI aqueous phase, such as piperazine (PIP), to obtain a more compact active layer. A novel kind of pH-stable positively charged composite NF membrane with excellent rejection performances was developed via interfacial polymerization on the surface of a polysulfone (PSF) UF substrate, using the mixture of PEI and PIP as the monomers of the aqueous phase, and CC as the monomer of the organic phase. The rejection performances, the chemical structures, the morphologies, and the stabilities of the resultant PEI composite NF membranes at extreme pH conditions have been investigated systematically and compared with the conventional PA composite NF membranes

Materials and chemicals
Membrane preparation
Characterizations of the resultant membranes
Rejection performances of the resultant composite NF membranes
MWCO measurement
Acid and alkali-resistance performances of the resultant composite membranes
Characterizations of membranes
Acid and alkali-resistance performances of the membranes
Conclusions
Conflicts of interest
Full Text
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