L-Lysine-Coated Magnetic Core-Shell Nanoparticles for the Removal of Acetylsalicylic Acid from Aqueous Solutions.

Nanotechnologies based on magnetic materials have been successfully used as efficient and reusable strategies to remove pharmaceutical residuals from water. This paper focuses on the fabrication, characterization, and application of ferrite-based magnetic nanoparticles functionalized with L-lysine as potential nanoadsorbents to remove acetylsalicylic acid (ASA) from water. The proposed nanomaterials are composed of highly magnetic and chemically stable core-shell nanoparticles covered with an adsorptive layer of L-lysine (CoFe2O4-γ-Fe2O3-Lys). The nanoadsorbents were elaborated using the coprecipitation method in an alkaline medium, leading to nanoparticles with two different mean sizes (13.5 nm and 8.5 nm). The samples were characterized by XRD, TEM, FTIR, XPS, Zetametry, BET, and SQUID magnetometry. The influence of time, pH, and pollutant concentration was evaluated from batch studies using 1.33 g/L of the nanoadsorbents. The Freundlich isotherm best adjusted the adsorption data. The adsorption process exhibited a pseudo-second-order kinetic behavior. The optimal pH for adsorption was around 4-6, with a maximum adsorption capacity of 16.4 mg/g after 150 min of contact time. Regeneration tests also showed that the proposed nanomaterials are reusable. The set of results proved that the nanoadsorbents can be potentially used to remove ASA from water and provide relevant information for their application in large-scale designs.

Hybrid magnetic CoFe2O4@γ-Fe2O3@CTAB nanocomposites as efficient and reusable adsorbents for Remazol Brilliant Blue R dye.

The main goal of the present survey was to elaborate, characterize and evaluate the efficiency of ferrite-based nanoparticles modified with cetyltrimethylammonium bromide (CTAB) as potential magnetic nanoadsorbents to remove Remazol Brilliant Blue R (RBBR) from water. It is proposed an innovative nanomaterial architecture based on highly magnetic and chemically stable core@shell nanoparticles covered by an adsorptive surface layer of CTAB (CoFe2O4@γ-Fe2O3@CTAB). Samples of two different mean sizes (7.5 and 14.6 nm) were synthesized using a hydrothermal coprecipitation followed by surface treatment and functionalization. Batch tests were performed to evaluate the influence of contact time, temperature, pH, shaking rate, presence of interferents and mean size on the performance of the proposed nanomaterials. The kinetics of the adsorption process followed the pseudo-second-order model with an equilibrium time of 20 min. The adsorption capacity was estimated by the Langmuir isotherm model and was found to be 56.3 mg/g (smaller size) and 45.6 mg/g (larger size) at pH = 3 and a shaking rate of 400 rpm. The process was spontaneous, exothermic, and showed increased randomness. Sulphate ions negatively impacted the removal of RBBR. The best performance of the nanoadsorbent based on smaller mean sizes can be correlated to its larger surface area. Regeneration and readsorption tests showed that the nanoadsorbents retain more than 80% of their original removal capacity, therefore they can be effectively recycled and reused.

Colloidal Stability and Concentration Effects on Nanoparticle Heat Delivery for Magnetic Fluid Hyperthermia.

The heat produced by magnetic nanoparticles, when they are submitted to a time-varying magnetic field, has been used in many auspicious biotechnological applications. In the search for better performance in terms of the specific power absorption (SPA) index, researchers have studied the influence of the chemical composition, size and dispersion, shape, and exchange stiffness in morphochemical structures. Monodisperse assemblies of magnetic nanoparticles have been produced using elaborate synthetic procedures, where the product is generally dispersed in organic solvents. However, the colloidal stability of these rough dispersions has not received much attention in these studies, hampering experimental determination of the SPA. To investigate the influence of colloidal stability on the heating response of ferrofluids, we produced bimagnetic core@shell NPs chemically composed of a ZnMn mixed ferrite core covered by a maghemite shell. Aqueous ferrofluids were prepared with these samples using the electric double layer (EDL) as a strategy to maintain colloidal stability. By starting from a proper sample, ultrastable concentrated ferrofluids were achieved by both tuning the ion/counterion ratio and controlling the water content. As the colloidal stability mainly depends on the ion configuration on the surface of the magnetic nanoparticles, different levels of nanoparticle clustering are achieved by changing the ionic force and pH of the medium. Thus, the samples were submitted to two procedures of EDL destabilization, which involved dilution with an alkaline solution and a neutral pH viscous medium. The SPA results of all prepared ferrofluid samples show a reduction of up to half the efficiency of the standard sample when the ferrofluids are in a neutral pH or concentrated regime. Such results are explained in terms of magnetic dipolar interactions. Our results point to the importance of ferrofluid colloidal stability in a more reliable experimental determination of the NP heat generation performance.