Background. Dyes are one of the most hazardous materials in industrial effluents which can cause several health problems in living organisms. The removal of dye from colored effluents has attracted increasing attention in the last decade. In this study, raw, beneficiated, and activated waste ash were evaluated as adsorbents for removal of methylene blue (MB) from aqueous solution by the batch adsorption method. Comprehensive characterization studies were carried out on each bioadsorbent, such as proximate analyses, bulk density, specific surface area, point of zero charge, pH, and Fourier transform infrared (FTIR) spectroscopy (which shows functional groups on adsorbents surface). The effects of pH, adsorbent dosage, initial dye concentration, and contact time were determined in order to know the optimum condition and adsorption potential of the adsorbents. The methylene blue (MB) removal efficiency of raw, beneficiated, and activated bioadsorbents from aqueous solutions was found to be 95.212%, 89.172%, and 84.504%, respectively. It is reported that adsorption efficiency of MB on each adsorbent was quite different due to electrostatic and dispersion interaction between the dye molecules and the surface property of the adsorbents. The obtained results were well fitted with the Freundlich isotherm model, and the adsorption process follows the pseudo-second-order kinetics model for all adsorbents. In fact, the results showed that raw, beneficiated, and activated waste ash bioadsorbents could be employed as effective and economical alternative material in the near future.

The aim of this study was to investigate the adsorption characteristics of malachite green (MG) dye onto the raw (RLAPW) and activated (ALAPW) surface of Lupinus albus seed peel waste prepared via physicochemical activation under alkaline condition as a dye adsorbent. Proximate analysis, surface area (Sears method), point of zero charge (pHzpc), and FTIR analysis were used to characterize the adsorbents. The effects of operational parameters such as pH (4) for ALAPW and pH (6) for RLAPW, adsorbent dose (0.2g), initial dye concentration (30mg/L), contact time (60min), and temperature (298K) were optimized. The experimental data well fitted with the Freundlich adsorption isotherm with the adsorption capacity of 7.3mg/g for activated Lupinus albus seed peel waste (ALAPW) and Sips isotherm for raw Lupinus albus seed peel waste (RLAPW) with the adsorption capacity of 6.6mg/g. The kinetics data well fitted to pseudo-second-order kinetic model for both adsorbents. Thermodynamic study revealed that the bioadsorption process using bioadsorbents was spontaneous and exothermic in nature. Desorption experiment was conducted and showed desorption efficiency at an acidic pH of 2. The results showed that the prepared adsorbents exhibited good adsorption capacity and can be used as an alternative adsorbent for the adsorptive removal of malachite green dyes.

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.