180
Views
2
CrossRef citations to date
0
Altmetric
Original Articles

Novel positively charged chiral chitosan composite nanofiltration membrane

, , &
Pages 33-38 | Received 11 Oct 2013, Accepted 18 Feb 2014, Published online: 26 Mar 2014
 

Abstract

Chitosan was modified with a chiral compound and a positively charged compound. Series of novel composite nanofiltration (NF) memebranes were prepared by over-coating the polysulfone ultrafiltration membrane with the mixture of chitosan and chitosan derivative. The chiral compound, the positively charged compound and their chitosan derivatives were characterised by infrared spectrophotometer (IR) and polarimeter. The structure of the membrane was characterized by scanning electron microscopy (SEM). The performance of membrane was strictly related to the chiral compound and the positively charged compound grafted to chitosan and its composition. The rejection of P2–7 composite NF membrane reached the maximum of 95·2%, and the flux remained to be as high as 687·4 L m−2 h−1 at 0·4 MPa with 1000 mg L−1 CaCl2. Electrostatic effect had no effect on NaCl, while excellent effect on CaCl2. It was typical positively charged NF membrane, which was suitable for separating the multivalent cation solutes from the feed solution.

Acknowledgement

Financial support from the National Key Technology Support Program of China (no. 2008BAL55B03) is gratefully acknowledged.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.