This study assessed the applicability of Fe-impregnated biochar derived from cattle manure (Fe-CMB) as an adsorbent for removing Sb(V) from aqueous solutions and investigated the Sb(V) adsorption mechanism. Fe-CMB was mainly composed of C, O, Cl, Fe, Ca, and P, and the adsorption of Sb(V) onto Fe-CMB was identified using an energy dispersive spectrometer and Fourier transform infrared spectroscopy. Sb(V) adsorption reached equilibrium within 6 h, and the Sb(V) adsorption data as a function of time were well described by the pseudo-second-order model. The Langmuir isotherm model fit the equilibrium data better than the Freundlich model. The maximum adsorption capacity of Fe-CMB for Sb(V) obtained from the Langmuir model was 58.3 mg/g. Thermodynamic analysis of Sb(V) adsorption by Fe-CMB indicated that the adsorption process was exothermic and spontaneous. The Sb(V) removal percentage increased with the Fe-CMB dose, which achieved a removal of 98.5% at 10.0 g/L Fe-CMB. Increasing the solution pH from 3 to 11 slightly reduced Sb(V) adsorption by 6.5%. The inhibitory effect of anions on Sb(V) adsorption followed the order: Cl− ≈ NO3− < SO42− < HCO3− < PO43−.
Although the level of neuroscience research is rapidly developing with the introduction of new technologies, the method of neuroanatomy education remains at the traditional level and requires improvement to meet the needs of educators and trainees. We developed a new three-dimensional (3D) printed device (human braincutting mold, HBCM) for creating human brain slices; moreover, we demonstrated a simple method for creating semi-permanent ultraviolet (UV) resin-mounted brain slice specimens for neuroanatomy education. We obtained brain slices of uniform thickness (3 mm) through the HBCM; the resultant brain slices were optimal for assessing morphological details of the human brain. Furthermore, we used an agar-embedding method for brain-slicing with the HBCM, which minimized geometrical distortions of the brain slices. Also, we prepared semi-permanent brain serial specimens using an acrylic brain slice frame and UV-curable resin, which was highly compatible with moist bio-specimens. During UV resin curing, neither air bubble formation nor color change occurred. The resultant UV resin-mounted brain slices produced definite coronal sections with high transparency and morphological accuracy. We also performed 3D modeling by stacking brain slice images that differentiated the cortical area and nine subcortical regions via manual segmentation. This method could be a reliable alternative for displaying high-quality human brain slices and would be helpful for students and trainee to understand anatomical orientation from 2D images to 3D structures. Also, this may present an innovative approach for preparing and preserving coronal sections of the normal or pathological human brain.
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