The microstructures of the activated carbon black microparticles (ACBMPs) generated through both treatments of 20 min ultrasonic and 400 °C thermal energy equivalent have been analyzed properly using scanning electron microscope (SEM), X-ray diffraction (XRD) and Fourier-transformed infrared (FTIR) spectroscopy methods. The research was aiming to generate binding or active sites points on the outer surface of the ACBMPs body of which commonly plays an important role in both adsorption and catalytic processes. It was observed that around 150 nm up to 400 nm in average diameter super macro voids with many various turns of nano-scale wells, and around 1.84 angstrom (Å) up to 15.98 Å intraparticle pores were generated. In addition, the parallel planes spacing of the carbonaceous framework sheets, namely d hkl in Miller indexes terminology, of about 4.44 Å up to 2.98 Å constructed the inner particles of the ACBMPs body. A new nomenclature method for the binding or active site shapes identification and classifying them into four categories based on the quadrants terminology, i.e. quadrant one (Q1), two (Q2), three (Q3) and four (Q4) is proposed. Each the quadrants contains four categories of turns types, i.e. sharp, semi sharp, obtuse and non-significant turns depending on the angle of the associated turn in radian angle, θ. Finally, it can be concluded that the combination of ultrasonic and thermal energy treatments in fabricating ACBMPs could generate binding or active site points with unique shapes as a transit terminal for any guest molecules, in this context is methyl red (MR) molecules to enter into the suitable intra-particles pores of the ACBMPs body.
This study assesses the optical properties and conductivity of PVA-H3PO4 (polyvinyl alcohol-phosphoric acid) polymer film blend irradiated by gamma (γ) rays. The PVA-H3PO4 polymer film blend was prepared by the solvent-casting method at H3PO4 concentrations of 75 v% and 85 v%, and then irradiated up to 25 kGy using γ-rays from the Cobalt-60 isotope source. The optical absorption spectrum was measured using an ultraviolet-visible spectrophotometer over a wavelength range of 200 to 700 nm. It was found that the absorption peaks are in three regions, namely two peaks in the ultraviolet region (310 and 350 nm) and one peak in the visible region (550 nm). The presence of an absorption peak after being exposed to hυ energy indicates a transition of electrons from HOMO to LUMO within the polymer chain. The study of optical absorption shows that the energy band gap (energy gap) depends on the radiation dose and the concentration of H3PO4 in the polymer film blend. The optical absorption, absorption edge, and energy gap decrease with increasing H3PO4 concentration and radiation dose. The interaction between PVA and H3PO4 blend led to an increase in the conductivity of the resulting polymer blend film.
This research aimed to enhance the antibacterial activity of silver nanoparticles (AgNPs) synthesized from silver nitrate (AgNO3) using aloe vera extract. It was performed by means of incorporating AgNPs on an activated carbon nanoparticle (ACNPs) under ultrasonic agitation (40 kHz, 2 × 50 watt) for 30 min in an aqueous colloidal medium. The successful AgNPs synthesis was clarified with both Ultraviolet-Visible (UV-Vis) and Fourier Transform Infrared (FTIR) spectrophotometers. The successful AgNPs-ACNPs incorporation and its particle size analysis was performed using Transmission Electron Microscope (TEM). The brown color suspension generation and UV-Vis's spectra maximum wavelength at around 480 nm confirmed the existence of AgNPs. The particle sizes of the produced AgNPs were about 5 to 10 nm in the majority number, which collectively surrounded the aloe vera extract secondary metabolites formed core-shell like nanostructure of 8.20 ± 2.05 nm in average size, while ACNPs themselves were about 20.10 ± 1.52 nm in average size formed particles cluster, and 48.00 ± 8.37 nm in average size as stacking of other particles. The antibacterial activity of the synthesized AgNPs and AgNPs-immobilized ACNPs was 57.58% and 63.64%, respectively (for E. coli); 61.25%, and 93.49%, respectively (for S. aureus). In addition, when the AgNPs-immobilized ACNPs material was coated on the cotton and polyester fabrics, the antibacterial activity of the materials changed, becoming 19.23% (cotton; E. coli), 31.73% (polyester; E. coli), 13.36% (cotton; S. aureus), 21.15% (polyester; S. aureus).