| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 175289 | Dyes and Pigments | 2016 | 9 Pages |
•Propyl-1-N,N-di-succinamic acid functionalized MCM-41(SA-MCM-41) was synthesized.•The removal of rhodamine 6G, methylene blue and metanil yellow was tested.•The SA-MCM-41 can remove metanil yellow effectively in presence of rhodamine 6G.•The adsorption from mixture of dyes following a multilayer mechanism.
The adsorption properties of succinamic acid functionalised MCM-41 (SA-MCM-41) towards dyes aqueous solution, such as rhodamine 6G (R6G), methylene blue (MB) and metanil yellow (MY), were studied. SA-MCM-41 was synthesised using a three step synthesis strategy, starting with the preparation of MCM-41 through a sol–gel methodology. Succinamic acid functionality was introduced through a ring opening reaction of succinic anhydride (SA) over the propyl amine functionality of A-MCM-41 in presence of trimethylamine. The materials at each synthesis step were characterised by X-ray diffraction, transmission electron microscopy, scanning electron microscopy, N2 adsorption–desorption isotherms, Fourier transform infrared spectroscopy, and 29Si and 13C nuclear magnetic resonance spectroscopies. SA-MCM-41 exhibited good adsorption capacity towards R6G and MB but poor adsorption for MY from the individual dye solutions. The competitive adsorption from binary and ternary dye mixtures showed that SA-MCM-41 can remove MY effectively in the presence of R6G. The adsorption behaviour of R6G and MY over SA-MCM-41 from binary and ternary mixtures highlight the possibility of multilayer adsorption. The MY removal efficiency of pristine MCM-41 from R6G-MY binary mixture was also tested.
Graphical abstractFigure optionsDownload full-size imageDownload as PowerPoint slide
