Sludge-derived alginate-like extracellular polymers (ALE) for preparation of Fe-ALE and FeCaMg-ALE: Application to the adsorption of phosphate.

Excess phosphorus (P) in wastewater has potential risk of causing harmful algal bloom and eutrophication in receiving wastewater. In this study, alginate-like extracellular polymers (ALE) derived from conventional activated sludge were modified with ionic cross-linking agents (Fe3+, Ca2+, and Mg2+) to develop Fe-ALE and FeCaMg-ALE for the adsorption of phosphate from wastewater. The adsorption process of phosphate by Fe-ALE and FeCaMg-ALE can be well described by pseudo-second-order kinetics and Freundlich isotherm model with a high level of accuracy, indicating that the adsorption processes were chemical, multi-layer adsorption process. The maximum adsorption capacity of dry Fe-ALE and FeCaMg-ALE concerning phosphate were 15.06 and 20.10 mg/g, respectively at 298 K. The adsorption capacity remained relatively consistent across a pH range of 2.0-11.0. FT-IR, XRD, SEM coupled with XPS analysis demonstrated the ALE had been successfully compounded with Fe3+ or Fe3+/Ca2+/Mg2+. Based on the experimental results and characteristic analysis, the main mechanism of phosphate by Fe-ALE and FeCaMg-ALE are physical filling, electrostatic attraction, ligand exchange and precipitation reaction. This work provides a new perspective for preparing ALE-based adsorbent using conventional activated sludge as raw material, realizing the treatment of waste with waste and effectively recovering phosphate from wastewater.

NiCo bimetallic and the corresponding monometallic organic frameworks loaded CMC aerogels for adsorbing Cu2+: Adsorption behavior and mechanism.

In this study, three-dimensional (3D) carboxymethylcellulose sodium (CMC) aerogel was decorated with NiCo bimetallic and the corresponding monometallic organic frameworks to prepare MOFs-CMC composite adsorbents for the removal of Cu2+. The obtained MOFs-CMC composite including Ni/Co-MOF-CMC, Ni-MOF-CMC, and Co-MOF-CMC were characterized by SEM, FT-IR, XRD, XPS analysis, and zeta potential. The adsorption behavior of MOFs-CMC composite for Cu2+ was explored by batch adsorption test, adsorption kinetics and adsorption isotherms. The experimental data satisfied the pseudo-second-order model and Langmuir isotherm model. The maximum adsorption capacities followed the sequence of Ni/Co-MOF-CMC (233.99 mg/g) > Ni-MOF-CMC (216.95 mg/g) > Co-MOF-CMC (214.38 mg/g), indicating that there was a synergistic effect between Ni and Co to promote the adsorption of Cu2+. Combining characterization analysis and density functional theory (DFT) calculation, it is clarified that the adsorption mechanism of MOFs-CMC for Cu2+ includes ion exchange, electrostatic interactions, and complexation.