The behavior of phosphate adsorption and its reactions on the surfaces of Fe–Mn oxide adsorbent
-
Add time:07/28/2019 Source:sciencedirect.com
A Fe–Mn oxide adsorbent (FMO) with the Fe/Mn molar ratio of 5:1 was combined to remove phosphate in aqueous solution. An apparently irregular surface and heterogeneous porous structure were found in the SEM images of FMO. XPS spectra showed that manganese and iron existed mainly in the +IV and +III oxidation states, respectively. Batch experiments were carried out to investigate the effect of contact time, initial phosphate concentration, temperature, pH and coexisting anions on phosphate removal. Kinetic data of phosphate adsorption onto FMO followed the pseudo-second-order kinetic model, indicating that the phosphate adsorption process was chemisorption. The equilibrium data were analyzed by both Freundlich and Langmuir isotherm models and the Langmuir isotherm model fitted better with the maximum adsorption capacity of 18.4 mg/g at 308 K and pH 7.0. Thermodynamic parameters demonstrated that the phosphate adsorption process was nonspontaneous and endothermic. The phosphate adsorption was critically dependent upon pH value with the maximum adsorption amounts occurring under acidic conditions and decreased with the increase of solution pH. Additionally, the terminal pH increased under acidic conditions while decreased under alkaline conditions. Coexisting anions of nitrate, silicate, sulfate and carbonate had no negative effect on the adsorption of phosphate, inferring the inner-sphere surface complexes were involved in the phosphate adsorption process. Phosphate adsorption by FMO was achieved by electrostatic attraction and replacement of hydroxyl groups. FMO, with large adsorption capability, is a promising attractive adsorbent for phosphate removal from water body.
We also recommend Trading Suppliers and Manufacturers of Manganese (II) phosphate, Mn 34% (cas 10236-39-2). Pls Click Website Link as below: cas 10236-39-2 suppliers
Prev:Comparative study on the oxidation of N,N-diethyl-3-methyl benzoyl amide by Mn(III) and peroxymonosulfate/Co(II): Selective and nonselective oxidation
Next:Tumor acidity-activatable manganese phosphate nanoplatform for amplification of photodynamic cancer therapy and magnetic resonance imaging) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information
- A novel catalase mimicking nanocomposite of Mn(II)-poly-L-histidine-carboxylated multi walled carbon nanotubes and the application to hydrogen peroxide sensing08/01/2019
- Manganese alters expression of proteins involved in the oxidative stress of Meyerozyma guilliermondii07/31/2019
- Simultaneous nutrients (N,P) removal by using a hybrid inorganic sorbent impregnated with hydrated manganese oxide07/30/2019
- Tumor acidity-activatable manganese phosphate nanoplatform for amplification of photodynamic cancer therapy and magnetic resonance imaging07/29/2019
- Comparative study on the oxidation of N,N-diethyl-3-methyl benzoyl amide by Mn(III) and peroxymonosulfate/Co(II): Selective and nonselective oxidation07/27/2019
- High-efficient synergistic extraction of Co(II) and Mn(II) from wastewater via novel microemulsion and annular centrifugal extractor07/26/2019
- The distribution of Mn(II)chemical forms on soybean roots as related to Mn(II) toxicity07/25/2019
- Rich growth medium promotes an increased on Mn(II) removal and manganese oxide production by Serratia marcescens strains isolates from wastewater07/24/2019
- Effect of Mn doping on the low-temperature synthesis of tricalcium phosphate (TCP) polymorphs07/23/2019
-
Health and Chemical more >


