With the temperature increasing up to 150°C and keeping it constant for 12.0 h, the products comprised uniform porous pod-like α-Fe2O3 with higher crystallinity (Belnacasan chemical structure Figure 2a 4) and multitudinal cavities on the surfaces (Figure

2e,f), 84% of which had a longitudinal length of 2.6 to 3.2 μm [44]. The morphology of the present pod-like α-Fe2O3 nanoarchitectures was somewhat similar to that of the melon-like microparticles by the controlled H2C2O4 etching process [25]. With the temperature further going up to 180°C, porous pod-like α-Fe2O3 nanoarchitectures Ipatasertib solubility dmso with further improved crystallinity (Figure 2a 5) and more and larger cavities on the surfaces were obtained (Figure 2g), 84% of which had a

longitudinal length of 2 to 2.4 μm (Figure 2g 1). When hydrothermally treated at 210°C for 12.0 h, the product evolved into high-crystallinity whereas entirely loose porous α-Fe2O3 nanoarchitectures (Figure 2a 6,h), 84% of which had a longitudinal length of 2.1 to 2.7 μm (Figure 2h 1). check details Figure 2 XRD patterns (a) and SEM images (b-h) of the hydrothermal products. The products were synthesized at different temperatures for 12.0 h, with the molar ratio of FeCl3/H3BO3/NaOH = 2:3:4. Temperature (°C) = 90 (a1, b), 105 (a2, c), 120 (a3, d), 150 (a4, e, f), 180 (a5, g), 210 (a6, h). Inset: high-resolution SEM image (c1) as well as the longitudinal length distributions (d1, g1, h1) of the corresponding samples. The asterisk represents hematite (α-Fe2O3, JCPDS No. 33–0664); nabla represents akaganeite

(β-FeOOH, JCPDS No. 34–1266). It was worth noting that when treated at a temperature from 90°C to 210°C for 12.0 h, the overall crystallinity of the products became higher (Figure 2a 2,a3,a4,a5,a6), and the NPs and cavities within the α-Fe2O3 nanoarchitectures grew larger. The product evolved from compact pod-like nanoarchitectures (Figure 2c,d) to loose (Figure 2e,f) and to looser (Figure 2g,h) pod-like nanoarchitectures. As a matter of fact, Cyclic nucleotide phosphodiesterase with the temperature going up from 120°C to 150°C, to 180°C, and to 210°C, the crystallite size along the [104] direction, i.e., D 104, calculated by the Debye-Scherrer equation also increased from 23.3 to 27.3, to 28.0, and to 31.3 nm, respectively. This was in accordance with the direct observation on the gradual increase in the NP size within the nanoarchitectures (Figure 2d,e,f,g,h), thus accounted for the gradual sharper tendency for the XRD patterns of the corresponding hydrothermal products (Figure 2a 3,a4,a5,a6) obtained from 120°C to 210°C. Analogous to those obtained previously (Figure 1c,e,f), the nanoarchitectures obtained at 150°C to 210°C for 12.0 h were speculated to be constituted of 1D assemblies (Figure 2e,f) or NPs (Figure 2g,h).