RESUMO
Nowadays, substituting petroleum-based plastics with biodegradable polymers made from polysaccharides loaded with various reinforcing materials has recently gained attention due to the impact of conventional plastics wastes. In this study, polysaccharidic mucilage from Ethiopian cactus (Opuntia Ficus Indica) was derived using microwave-assisted extraction technique to develop biodegradable polymers that were inexpensive, readily available, simple to make, and ecofriendly. The effect of microwave power 300-800 W, solid-liquid (cactus-sodium hydroxide solution) ratio 1:5-1:25, sodium hydroxide concentration 0.1-0.8 mol/L, and extraction time 2-10 min on mucilage extraction were studied and the maximum yield of mucilage was attained at optimized parameters of 506 W, 1:20, 0.606 mol/L, and 9.5 min, respectively. Biodegradable polymers made with mucilage alone have poor mechanical characteristics and are thermally unstable. Thus, to overcome the stated problems, glycerol as a plasticizer and acid-leached kaolin crosslinked with urea as a reinforcing material were used. Moreover, the effect of acid-leached kaolin and glycerol on the physico-chemical properties of the films was studied, and a maximum tensile strength of 6.74 MPa with 18.45 % elongation at break, thermally improved biodegradability of 26 %, were attained at 10 % acid-leached kaolin and 20 % glycerol crosslinking with 2 % urea. But the maximum degradability of 53.5 % was attained at 30 % glycerol content. The control and reinforced biodegradable films were characterized using TGA, FTIR, SEM, and XRD to determine the thermal, functional group, morphology, and crystallinity of the bioplastics, respectively. These biodegradable plastics may be used for packaging application.
RESUMO
Ag doped Co3O4 nanoparticles (NPs) were synthesized via a co-precipitation method changing the concentration of Ag. The crystal structure, morphology, surface area, functional group, optical band gap, and thermal property were investigated by XRD, SEM, BET, FTIR, UV-Vis, and TGA/DTA techniques. The XRD results showed the formation of single-cubic Co3O4 nanostructured materials with an average crystal size of 19.37 nm and 12.98 nm for pristine Co3O4 and 0.25 M Ag-doped Co3O4 NPs. Morphological studies showed that pristine Co3O4 and 0.25 M Ag-doped Co3O4 NPs having a porous structure with small spherical grains, porous structures with sponge-like structures, and loosely packed porous structures, respectively. The pristine and 0.25 M Ag-doped Co3O4 NPs showed BET surface areas of 53.06 m2/g, and 407.33 m2/g, respectively. The band gap energy of Co3O4 NPs were 2.96 eV, with additional sub-bandgap energy of 1.95 eV. Additionally, it was discovered that the band gap energies of 0.25 M Ag-doped Co3O4 NPs ranged from 2.2 to 2.75 eV, with an extra sub-band with energies ranging from 1.43 to 1.94 eV for all as-prepared samples. The Ag-doped Co3O4 as prepared samples show improved thermal properties due to the doping effect of silver. The CV test confirmed that the 0.25 M Ag-doped Co3O4 NPs exhibited the highest specific capacitance value of 992.7 F/g at 5 mV/s in a 0.1 M KOH electrolyte solution. The energy density and power density of 0.25 M Ag-doped Co3O4 NPs were 27.9 W h/kg and 3816.1 W/kg, respectively.
