8% volume fraction of nanoparticles were investigated using an AC magnetic field generator with H = 20 kA m-1 and f = 120 kHz. The schematic representation of the used apparatus is shown in Figure  1. The samples and process conditions are summarized in Table  1. Figure 1 Schematic representation of the experimental setup for inspecting the inductive properties of magnetic VX-689 fluids. Table 1 Samples and process condition AMN-107 in vivo Sample Water/surfactant molar ratio (R) T (K) W1 7 300 W2 14 300 W3 20 300 W4 27 300 A1 – 623 A2 – 823 Results and discussion Structural characterization Figure  2a shows the high-resolution TEM image of the W4 sample.

The bad crystallinity of as-synthesized nanoparticles is due to fast borohydride reduction which prevents lattice planes from being arranged in a complete crystalline manner. Electron beam and AZD1152 clinical trial X-ray diffraction patterns

(Figure  2b,d) indicate the formation of a bcc-structured iron-cobalt alloy. Also, a small quantity of CoFe2O4 (at 2θ = 35.4°, 62.4°) is observed due to partial oxidation of the sample due to the exposure of nanoparticles to air. This also is confirmed by the presence of an oxygen peak in the EDS spectrum in Figure  2c. Therefore, it could be inferred that a thin oxide film has been formed around the synthesized nanoparticles. The EDS analysis also shows Fe and Co peaks in which the Fe peak is sharper, indicating higher content of Fe than Co. Figure 2 Characterization of the W4 sample. (a) HRTEM micrograph. (b) Selected area diffraction pattern. (c) EDS spectrum. (d) XRD patterns. Figure  3 shows the effect of water-to-surfactant molar ratio (R) on the morphology,

size, and size distribution of as-synthesized nanoparticles. The mean size and size distribution Farnesyltransferase for each specimen were determined by inspecting about 50 TEM micrographs. It is evident that all samples have spherical shape due to the nature of the oil-surfactant-water system used. Figure 3 TEM micrographs of as-synthesized nanoparticles and corresponding size distributions. (a) W1, (b) W2, (c) W3, (d) W4, (e) A1 (W4 annealed at 623 K) for 10 min, and (f) A2 (W4 annealed at 823 K) for 10 min. Figure  3 shows an expected increase in the mean size of nanoparticles with R because as the R value increases, the relative amount of water increases and a larger micelle would be obtained; thus, the limiting stability of nanoreactors decreases, leading to larger nanoparticles. It should be noted that at R > 27, the transparent microemulsion could not form, indicating that the maximum available R for this ternary system is 27. This means that with the ternary system of water/CTAB/hexanol, the maximum achievable size for the FeCo nanoparticle is about 7 nm. Figure  3e,f shows TEM images of the W3 sample annealed at 623 and 823 K for 10 min, respectively. It is seen that nanoparticles have grown by the fusion of smaller nanoparticles to the mean sizes of 36 and 60 nm, respectively.