Loading…
Magnetic Fe 3 O 4 /polypyrrole‐salicylaldehyde composite for efficient removal of Mn ( VII ) from aqueous solution by double‐layer adsorption
Fe 3 O 4 acted as the inner core, conducting polymer polypyrrole (PPy) was wrapped on the surface of Fe 3 O 4 , and salicylaldehyde (SA) was grafted to prepare the Fe 3 O 4 /PPy‐SA composite. Fe 3 O 4 /PPy‐SA exhibited double adsorption properties for Manganese (Mn) (VII) from aqueous solution. And...
Saved in:
Published in: | Journal of applied polymer science 2022-07, Vol.139 (28) |
---|---|
Main Authors: | , , , , , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | Fe
3
O
4
acted as the inner core, conducting polymer polypyrrole (PPy) was wrapped on the surface of Fe
3
O
4
, and salicylaldehyde (SA) was grafted to prepare the Fe
3
O
4
/PPy‐SA composite. Fe
3
O
4
/PPy‐SA exhibited double adsorption properties for Manganese (Mn) (VII) from aqueous solution. And the adsorption properties were systematically investigated. The influences of pH, initial metal ion concentration and temperature on the adsorption performance were measured, showing that the optimal adsorption pH is 2. Moreover, it was found that the adsorption kinetics followed the pseudo second order model, the initial adsorption rate was 46.1467 mg/g/min, and the process was controlled by the liquid film diffusion. The Langmuir adsorption isotherm model could describe the adsorption process well, and the increase of metal ion concentration and temperature was beneficial to the adsorption process. At 288.15 K, the maximum equilibrium adsorption capacity was 471.6981 mg/g. Thermodynamic parameters indicated that the adsorption process was spontaneous, endothermic, and entropy increment. Meanwhile, the cycle test results showed that the adsorbent has good cycle performance and broad application prospects. |
---|---|
ISSN: | 0021-8995 1097-4628 |
DOI: | 10.1002/app.52515 |