Superparamagnetic Spinel-Ferrite Nano-Adsorbents Adapted for Hg2+, Dy3+, Tb3+ Removal/Recycling: Synthesis, Characterization, and Assessment of Toxicity.

In the present work, superparamagnetic adsorbents based on 3-aminopropyltrimethoxy silane (APTMS)-coated maghemite (γFe2O3@SiO2-NH2) and cobalt ferrite (CoFe2O4@SiO2-NH2) nanoparticles were prepared and characterized using transmission-electron microscopy (TEM/HRTEM/EDXS), Fourier-transform infrared spectroscopy (FTIR), specific surface-area measurements (BET), zeta potential (ζ) measurements, thermogravimetric analysis (TGA), and magnetometry (VSM). The adsorption of Dy3+, Tb3+, and Hg2+ ions onto adsorbent surfaces in model salt solutions was tested. The adsorption was evaluated in terms of adsorption efficiency (%), adsorption capacity (mg/g), and desorption efficiency (%) based on the results of inductively coupled plasma optical emission spectrometry (ICP-OES). Both adsorbents, γFe2O3@SiO2-NH2 and CoFe2O4@SiO2-NH2, showed high adsorption efficiency toward Dy3+, Tb3+, and Hg2+ ions, ranging from 83% to 98%, while the adsorption capacity reached the following values of Dy3+, Tb3+, and Hg2+, in descending order: Tb (4.7 mg/g) > Dy (4.0 mg/g) > Hg (2.1 mg/g) for γFe2O3@SiO2-NH2; and Tb (6.2 mg/g) > Dy (4.7 mg/g) > Hg (1.2 mg/g) for CoFe2O4@SiO2-NH2. The results of the desorption with 100% of the desorbed Dy3+, Tb3+, and Hg2+ ions in an acidic medium indicated the reusability of both adsorbents. A cytotoxicity assessment of the adsorbents on human-skeletal-muscle derived cells (SKMDCs), human fibroblasts, murine macrophage cells (RAW264.7), and human-umbilical-vein endothelial cells (HUVECs) was conducted. The survival, mortality, and hatching percentages of zebrafish embryos were monitored. All the nanoparticles showed no toxicity in the zebrafish embryos until 96 hpf, even at a high concentration of 500 mg/L.

Removal of Pb2+, CrT, and Hg2+ Ions from Aqueous Solutions Using Amino-Functionalized Magnetic Nanoparticles.

In this paper, a circular economy approach with the adsorption and desorption of heavy metal (HM) ions­i.e., lead (Pb2+), chromium (CrT), and mercury (Hg2+)­from aqueous solutions was studied. Specific and selective binding of HM ions was performed on stabilized and amino-functionalized iron oxide magnetic nanoparticles (γ-Fe2O3@NH2 NPs) from an aqueous solution at pH 4 and 7. For this purpose, γ-Fe2O3@NH2 NPs were characterized by thermogravimetric analysis (TGA), Fourier-transform infrared spectroscopy (FTIR), specific surface area (BET), transmission electron microscopy (TEM), EDXS, and zeta potential measurements (ζ). The effects of different adsorbent amounts (mads = 20/45/90 mg) and the type of anions (NO3−, Cl−, SO42−) on adsorption efficiency were also tested. The desorption was performed with 0.1 M HNO3. The results showed improvement of adsorption efficiency for CrT, Pb2+, and Hg2+ ions at pH 7 by 45 mg of g-Fe2O3@NH2 NPs, and the sequence was as follows: CrT > Hg2+ > Pb2+, with adsorption capacities of 90.4 mg/g, 85.6 mg/g, and 83.6 mg/g, respectively. The desorption results showed the possibility for the reuse of γ-Fe2O3@NH2 NPs with HNO3, as the desorption efficiency was 100% for Hg2+ ions, 96.7% for CrT, and 91.3% for Pb2+.

Insights into Adsorption Characterization of Sulfated Xylans onto Poly(ethylene terephthalate).

The main aim of this investigation was to study the interaction of sulfated xylans as antithrombotic substances with poly(ethylene terephthalate) (PET) model films as a model for blood contacting surfaces. The adsorption of sulfated xylans onto PET model films was studied as a function of pH and ionic strength using the quartz crystal microbalance with dissipation (QCM-D) technique. The application of positively charged polyethyleneimine (PEI) as an anchoring polymer was done to improve the adsorption. The hydrophilic/hydrophobic properties of functionalized PET surfaces were monitored by goniometry, whilst their elemental composition was determined by X-ray photoelectron spectroscopy. Sulfated xylans adsorbed favorably at pH 5 by physical interactions and by entropy gain driven adsorption. Higher ionic strengths of solutions improved adsorption, due to the reduction of electrostatic repulsive forces between PET surfaces and anionic xylans' macromolecules. The intermediate PEI layer caused more extensive and stable adsorption due to Coulomb interactions. The surface modifications presented in this work provided important information regarding the adsorption/desorption phenomena between antithrombotic sulfated xylans and PET surfaces. The latter is of great interest when preparing advanced polymer composite material such as functional antithrombotic PET surfaces for blood-contacting medical devices and presents an extremely challenging research field.