3 research outputs found
Magnetic Porous Polymers Prepared via High Internal Phase Emulsions for Efficient Removal of Pb<sup>2+</sup> and Cd<sup>2+</sup>
Magnetic
porous polymers (MPPs) were successfully fabricated by
a facile strategy of the high internal phase emulsions (HIPEs) technique.
The microstructure, chemical composition, and magnetic properties
of the MPPs were characterized. Impregnated with polyÂ(styrene-divinylbenzene),
stabilized by the amine-functionalized Fe<sub>3</sub>O<sub>4</sub> nanoparticles (Fe<sub>3</sub>O<sub>4</sub>–NH<sub>2</sub>), the as-prepared MPPs with rich pore hierarchy were employed to
removal Pb<sup>2+</sup> and Cd<sup>2+</sup> from aqueous solution.
The MPPs display outstanding removal capacities toward Pb<sup>2+</sup> (257 mg/g) and Cd<sup>2+</sup> (129 mg/g) within 15 min, and the
encapsulated Fe<sub>3</sub>O<sub>4</sub>–NH<sub>2</sub> nanoparticles
endow the MPPs with the ability of magnetic separation (30.15 emu/g).
Additionally, the results indicate that the adsorptions of Pb<sup>2+</sup> and Cd<sup>2+</sup> are strongly dependent on pH and ionic
strength, demonstrating that the interactions of Pb<sup>2+</sup> and
Cd<sup>2+</sup> were mainly dominated by outer-sphere surface complexation
and electrostatic attraction. The adsorption process is revealed by
thermodynamic parameters to be spontaneous and endothermic. Further
study demonstrates that the adsorption is involved in ion-exchange
and cation−π interactions (between heavy metals and aromatic
ring) on the surface of MPPs. Thus, feasible preparation of the MPPs
with high adsorption capacities, excellent regeneration, and easy
separation properties opens a new expectation in the potential application
for engineering
Biochar Derived from Sawdust Embedded with Molybdenum Disulfide for Highly Selective Removal of Pb<sup>2+</sup>
Surface
interactions between the adsorbents and heavy metal ions
play an important role in the adsorption process, and appropriately
decorating the material’s surface can significantly improve
the removal capacity of the adsorbents. So, the objective of this
study is to modify biochar by coating with molybdenum disulfide (MoS<sub>2</sub>) for enhancing the adsorption of Pb<sup>2+</sup>. The biochar
pyrolyzed at 600 °C was chosen as the base to combine the flowerlike
MoS<sub>2</sub> (MoS<sub>2</sub>@biochar) by solvothermal reaction,
in which the abundant S-containing functional groups may promote the
elimination of Pb<sup>2+</sup>. The prepared MoS<sub>2</sub>@biochar
exhibits excellent adsorption capacity (189 mg/g) to Pb<sup>2+</sup> in water solution. The adsorption of Pb<sup>2+</sup> maintains a
high level under the circumstance of coexisting ions (Mg<sup>2+</sup>, Ca<sup>2+</sup>, Co<sup>2+</sup>, and Cd<sup>2+</sup>), suggesting
the high selectivity for Pb<sup>2+</sup>. The adsorption mechanism
of Pb<sup>2+</sup> on MoS<sub>2</sub>@biochar is mainly ascribed to
the inner-sphere surface complexation, in particular, metal–sulfur
chemical complexation. The easily recycled MoS<sub>2</sub>@biochar
still has high adsorption capacity for Pb<sup>2+</sup>. This work
demonstrates that the MoS<sub>2</sub>@biochar is an excellent candidate
of adsorbent for Pb<sup>2+</sup> removal
Fabrication of Core–Shell CMNP@PmPD Nanocomposite for Efficient As(V) Adsorption and Reduction
Here, we prepared
novel carboxyl-functionalized Fe<sub>3</sub>O<sub>4</sub> nanoparticles
(CMNPs) coated with polyÂ(m-phenylenediamine)
(CMNP@PmPDs) without complicated premodification procedures. The CMNP@PmPDs
show well-defined core–shell structures and combine both the
facile separation properties of magnetic particles and the extraordinary
adsorption performance of polymers. The CMNP@PmPDs were employed to
investigate the influence of various environmental factors (initial
pH, ionic strength, etc.) on the removal of AsÂ(V) through batch experiments.
The CMNP@PmPDs display much better AsÂ(V) adsorption performance than
the CMNPs, and the adsorption capacity is enhanced from 51.2 mg g<sup>–1</sup> to 95.2 mg g<sup>–1</sup>. The CMNP@PmPDs
exhibit high magnetization (∼46.7 emu g<sup>–1</sup>), indicating their easy separation under an external magnetic field
in practical applications. The major reaction pathway involving the
reduction of AsÂ(V) to AsÂ(III) was identified by X-ray photoelectron
spectroscopy (XPS) analysis. The removal mechanisms can be explained
by the adsorption of AsÂ(V) on protonated imino and carboxyl groups
via electrostatic attraction, which is then reduced to AsÂ(III) by
amine groups. This study demonstrates the potential application of
CMNP@PmPDs as a low-cost and effective remediation strategy for the
removal of AsÂ(V) from wastewater