| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1516951 | Journal of Physics and Chemistry of Solids | 2011 | 9 Pages |
The adsorption and photodegradation behavior of methyl orange (MO) and fast green (FG) over ZnAl- and MgAl-based layered double hydroxide (LDH) adsorbents have been examined. ZnAl-LDHs were prepared with Zn/Al ratios of 2 to 4 by co-precipitation at pH 8. The ZnAl-LDHs and a commercial MgAl-LDH with a Mg/Al ratio of 3 were evaluated for their ability to adsorb MO and FG and for the photodegradation behavior of these dyes under UV irradiation. Structure analysis of the LDH–dyes-adsorbed complexes revealed that the adsorption produced two types of structures, an intercalation complex for MO and a surface-adsorbed complex for FG. The maximum adsorption of MO on the LDHs was significantly higher (more than tenfold) than FG. Results indicated the adsorption isotherms for the retention of both dyes by ZnAl- and MgAl-LDHs could be fitted to a Freundlich equation, showing a higher affinity for dyes on MgAl-LDH compared to those on ZnAl-LDH. The catalytic degradation ability of dye–LDH complex solid films on a quartz plate was superior to pure dye films under UV irradiation. The FG non-intercalated LDH complexes showed much faster photodegradation under UV irradiation than the MO–intercalated LDH complexes, which pointed to the important role of the LDH materials containing sensitized dyes in enhancing the generation of labile hydroxyl ions from the hydrophilic LDH surface.
► Adsorption properties of anionic dyes on layered double hydroxides (LDHs) were examined. ► Different types of structures for dyes–LDH complexes were determined according to each dye. ► Photoinduced degradations of methyl orange and fast green over LDHs were evaluated. ► Presence of LDHs certainly accelerated the degradation reaction of dyes under UV irradiation.
