Synthesis and Characterization of Hydrogel Droplets Containing Magnetic Nano Particles, in a Microfluidic Flow-Focusing Chip.

Magnetic hybrid hydrogels have exhibited remarkable efficacy in various areas, particularly in the biomedical sciences, where these inventive substances exhibit intriguing prospects for controlled drug delivery, tissue engineering, magnetic separation, MRI contrast agents, hyperthermia, and thermal ablation. Additionally, droplet-based microfluidic technology enables the fabrication of microgels possessing monodisperse characteristics and controlled morphological shapes. Here, alginate microgels containing citrated magnetic nanoparticles (MNPs) were produced by a microfluidic flow-focusing system. Superparamagnetic magnetite nanoparticles with an average size of 29.1 ± 2.5 nm and saturation magnetization of 66.92 emu/g were synthesized via the co-precipitation method. The hydrodynamic size of MNPs was changed from 142 nm to 826.7 nm after the citrate group's attachment led to an increase in dispersion and the stability of the aqueous phase. A microfluidic flow-focusing chip was designed, and the mold was 3D printed by stereo lithographic technology. Depending on inlet fluid rates, monodisperse and polydisperse microgels in the range of 20-120 µm were produced. Different conditions of droplet generation in the microfluidic device (break-up) were discussed considering the model of rate-of-flow-controlled-breakup (squeezing). Practically, this study indicates guidelines for generating droplets with a predetermined size and polydispersity from liquids with well-defined macroscopic properties, utilizing a microfluidic flow-focusing device (MFFD). Fourier transform infrared spectrometer (FT-IR) results indicated a chemical attachment of citrate groups on MNPs and the existence of MNPs in the hydrogels. Magnetic hydrogel proliferation assay after 72 h showed a better rate of cell growth in comparison to the control group (p = 0.042).

Covalently-Bonded Coating of L-Arginine Modified Magnetic Nanoparticles with Dextran Using Co-Precipitation Method.

In this study, L-arginine (Arg) modified magnetite (Fe3O4) nanoparticles (RMNPs) were firstly synthesized through a one-step co-precipitation method, and then these aminated nanoparticles (NPs) were, again, coated by pre-oxidized dextran (Dext), in which aldehyde groups (DextCHO) have been introduced on the polymer chain successfully via a strong chemical linkage. Arg, an amino acid, acts as a mediator to link the Dext to a magnetic core. The as-synthesized Arg-modified and Dext-coated arginine modified Fe3O4 NPs were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), Fourier transformation infrared spectroscopy (FT-IR), thermogravimetric analysis (TGA), and vibrating sample magnetometer (VSM). Both synthesized samples, XRD pattern and FT-IR spectra proved that the core is magnetite. FT-IR confirmed that the chemical bonds of Arg and Dext both exist in the samples. SEM images showed that the NPs are spherical and have an acceptable distribution size, and the VSM analysis indicated the superparamagnetic behavior of samples. The saturation magnetization was decreased after Dext coating, which confirms successive coating RMNPs with Text. In addition, the TGA analysis demonstrated that the prepared magnetic nanocomposites underwent various weight loss levels, which admitted the modification of magnetic cores with Arg and further coating with Dext.

Stress-Induced Grain Refinement in Hard Magnetic Mn52Al45.7C2.3 Fabricated Using the Ball-Milling Method.

Mn52Al45.7C2.3 flakes with different sizes were prepared with two distinct surfactant-assisted ball-milling methods using cylindrical and barrel containers. Different microstructure and magnetic properties were measured based on the sequence of the container shape and different ball-milling times (2, 5, and 10 h). Morphology investigations showed that for powders milled in a barrel container, the amount of τ-phase was more compared to the samples milled in a cylindrical container. Moreover, in the powders milled with barrel containers, considerably higher magnetic properties were obtained in terms of saturation magnetization (Ms) and remanent magnetization (Mr) compared to those powders milled with cylindrical containers. Magnetic properties were found to be a function of the ball-milling time. High remanent magnetization and saturation magnetization have been found for powders milled in barrel containers, whereas only mediocre remanent magnetization and saturation magnetization have been measured in the case of milling in cylindrical containers. The highest Ms = 52.49 emu g-1 and Mr = 24.10 emu g-1 were obtained for the powders milled in barrel containers for 2 h. The higher magnetic properties taken from the milling in barrel containers is due to the higher shear stress and more uniform strain distribution induced by the barrel configuration, resulting in the stable τ-phase at a reasonably low-strain microstructure.

Different Stages of Phase Transformation in the Synthesis of Nanocrystalline Sr-Hexaferrite Powder Prepared by a Gaseous Heat Treatment and Re-Calcination Method.

In this paper, the phase transformation in a gaseous heat treatment and re-calcination (GTR) process for preparing nanocrystalline Sr-hexaferrite powder using methane (CH4) was studied. The process included gaseous heat treatment and subsequent re-calcination. Phase composition of the powder and its physical properties were changed significantly owing to formation of different intermediate phases. Sr-hexaferrite powder was prepared by the conventional route as the precursor. The results were represented in a phase transformation map that showed the intermediate phases and clarified the transformation path during the process. As evidenced by the map, the process had four general stages: decomposition of hexaferrite, reduction of iron oxides to pure iron, re-oxidation of iron, and re-formation of hexaferrite with different properties and structure.

Anisotropic Magnetoresistance Evaluation of Electrodeposited Ni80Fe20 Thin Film on Silicon.

In this study, a simple growth of permalloy NiFe (Py) thin films on a semiconductive Si substrate using the electrochemical deposition method is presented. The electrodeposition was performed by applying a direct current of 2 mA/cm2 during different times of 120 and 150 s and thin films with different thicknesses of 56 and 70 nm were obtained, respectively. The effect of Py thickness on the magnetic properties of thin films was investigated. Field emission scanning electron microscopy (FESEM), energy-dispersive X-ray spectroscopy (EDS), atomic force microscopy (AFM), ferromagnetic resonance (FMR), anisotropic magnetoresistance (AMR), and magneto-optic Kerr effect (MOKE) analyses were performed to characterize the Py thin films. It was observed that the coercivity of the Py thin film increases by increasing the thickness of the layer. Microscopic images of the layers indicated granular growth of the Py thin films with different roughness values leading to different magnetic properties. The magnetic resonance of the Py thin films was measured to fully describe the magnetic properties of the layers. The magnetoresistance ratios of deposited Py thin films at times of 120 and 150 s were obtained as 0.226% and 0.235%, respectively. Additionally, the damping constant for the deposited sample for 120 s was estimated as 1.36 × 10-2, which is comparable to expensive sputtered layers' characteristics.

Reverse Magnetization Behavior Investigation of Mn-Al-C-(α-Fe) Nanocomposite Alloys with Different α-Fe Content Using First-Order Reversal Curves Analysis.

The reverse magnetization behavior for bulk composite alloys containing Mn-Al-C and α-Fe nanoparticles (NPs) has been investigated by hysteresis loops, recoil, and first-order reversal curves (FORC) analysis. The effect of adding different percentages of α-Fe (5, 10, 15, and 20 wt. %) on the magnetic properties and demagnetization behavior of Mn-Al-C nanostructured bulk magnets was investigated. The fabricated nanocomposites were characterized by XRD and VSM for structural analysis and magnetic behavior investigations, respectively. The demagnetization curve of the sample Mn-Al-C-5wt. % α-Fe showed a single hard magnetic behavior and showed the highest increase in remanence magnetization compared to the sample without α-Fe, and therefore this combination was selected as the optimal composition for FORC analysis. Magnetic properties for Mn-Al-C-5 wt. % α-Fe nanocomposite were obtained as Ms = 75 emu/g, Mr = 46 emu/g, Hc = 3.3 kOe, and (BH)max = 1.6 MGOe, indicating a much higher (BH)max than the sample with no α-Fe. FORC analysis was performed to identify exchange coupling for the Mn-Al-C-0.05α-Fe nanocomposite sample. The results of this analysis showed the presence of two soft and hard ferromagnetic components. Further, it showed that the reverse magnetization process in the composite sample containing 5 wt. % α-Fe is the domain rotation model.

The Effect of Trehalose Coating for Magnetite Nanoparticles on Stability of Egg White Lysozyme.

In this study, the protein stability of hen egg-white lysozymes (HEWL) by Fe3O4 and Fe3O4-coated trehalose (Fe3O4@Tre) magnetic nanoparticles (NPs) is investigated. For this purpose, the co-precipitation method was used to synthesize magnetic NPs. The synthesized NPs were characterized by XRD, FT-IR spectroscopy, FE-SEM, and VSM analysis. In addition, the stability of HEWLs exposed to different NP concentrations in the range of 0.001-0.1 mg mL-1 was investigated by circular dichroism (CD) spectroscopy, fluorescence, and UV-Vis analysis. Based on the results, in the NP concentration range of 0.001-0.04 mg mL-1 the protein structure is more stable, and this range was identified as the range of kosmotropic concentration. The helicity was measured at two concentration points of 0.02 and 0.1 mg mL-1. According to the results, the α-helix at 0.02 mg mL-1 of Fe3O4 and Fe3O4@Tre was increased from 35.5% for native protein to 37.7% and 38.7%, respectively. The helicity decreased to 36.1% and 37.4%, respectively, with increasing the concentration of Fe3O4 and Fe3O4@Tre to 0.1 mg mL-1. The formation of hydrated water shells around protein molecules occurred by using Fe3O4@Tre NPs. Hence, it can be concluded that the trehalose as a functional group along with magnetic NPs can improve the stability of proteins in biological environments.

Effect of Thermomechanical Treatment of Al-Zn-Mg-Cu with Minor Amount of Sc and Zr on the Mechanical Properties.

In this study, the mechanical and microstructural properties of Al-Zn-Mg-Cu-Zr cast alloy with 0.1% Sc under homogeneous, dissolution, and T6 and thermomechanical treatments with the aim of increasing the volume fraction of MgZn2. Al3(Sc,Zr) reinforcing precipitates were examined by hardness, microscopic examinations, tensile tests and software analysis. The results showed that, firstly, the hardness results are well proportional to the results of the tensile properties of alloys and, secondly, the strength of the alloy with thermomechanical treatments compared to T6 treatments increased from 492 MPa to 620 MPa and the elongation increased from 8% to 17% and was 100% upgraded. Microstructural and fracture cross section investigations showed that Al3(Sc,Zr) nanosize dispersoids were evenly distributed among MgZn2 dispersoids and the alloy fracture was of semi-ductile type and nanosize dispersoids less than 10 nm were observed at the end of the dimples in the fracture section. The volume fraction of nanosize dispersoids in the whole microstructure of thermomechanical treatment samples was also much higher than that of T6 heat treated samples, so that the percentage of Al3(Sc,Zr) precipitates arrived from less than 1% in T6 operation to 8.28% in the quench-controlled thermomechanical operation (with 50% deformation). The quality index (QI) in thermomechanical treatment samples is 19% higher than T6 samples, so that this index has increased from 641 in T6 operation to 760 in samples under thermomechanical treatment due to precipitate morphology, volume fraction of precipitates, their uniform distribution in the matrix, and nano sized precipitates in samples under thermomechanical treatment.