A combined system including sonocatalysis and photocatalysis was applied for catalytic degradation of tetracycline (TC) antibiotic using TiO2 decorated on magnetic activated carbon (MAC@T) in coupling with ultraviolet (UV) and ultrasound (US) irradiations. MAC was fabricated via magnetization of AC using Fe3O4 nanoparticles. FESEM, EDS, TEM, BET, XRD, PL, VSM and UV-visible DRS techniques were used to characterize the catalyst features. The performance of MAC@T/UV/US system was examined under impact of different input variable such as catalyst loading, solution pH, initial TC concentration, US power, scavenging agents, chemical oxidants and co-exiting anions. The degradation rate was enhanced substantially when MAC@T coupled with US and UV irradiations. At optimal conditions, over 93% TC and 50% TOC were removed under 180 min reaction. Whereas, the complete removal of TC was obtained after 60 min treatment, when MAC@T/UV/US coupled with oxidants. Decreasing sequence of the inhibitory effect of anions was chloride > bicarbonate > phosphate > nitrate > sulfate. Both Fe leaching and loss of the decontamination were slight with reused times, indicating MAC@T has a high stability and reusability. According to trapping tests, holes, OH and 1O2 were contributed in the degradation process. In conclusion, integration of MAC@T composite and US/UV for enhancing catalytic degradation efficiency can be introduced as a successful and promising technique, owing to excellent catalytic activity, easy recovery, good adsorption capacity and high durability and recycling potential.

Recently, adsorption process has been introduced as a favorable and effective technique for the removal of metal ions from aqueous solutions. In the present study, bimetallic nanoparticles consisting of zero valent iron and silver were loaded on the activated carbon powder for the preparation of a new adsorbent (PAC-Fe^o/Ag). The above adsorbent was characterized by using XRD, SEM and TEM techniqes. Experimental data were exploited for kinetic, equilibrium and thermodynamic evaluations related to the adsorption processes. The Cr(VI) adsorption process was found to be favorable at pH 3 and it reached equilibrium state within 60 min. The stirring rate did not have a significant effect on the adsorption efficiency. Furthermore, the monolayer adsorption capacity of Cr(VI) based on the Langmuir model was measured to be 100 mg/g. The experimental equilibrium data were fitted to the Freundlich adsorption and pseudo second-order models. According to the thermodynamic study, the adsorption process was spontaneous and endothermic in nature, indicating the adsorption capacity increases with increasing the temperature. The results also revealed that the synthesized composite can be potentially applied as a magnetic adsorbent to remove Cr(VI) contaminants from aqueous solutions.

In this study, powder activated carbon (PAC) and magnetic nanoparticles of iron (III) oxide were used for synthesis of Fe₃O₄-activated carbon magnetic nanoparticles (AC-Fe₃O₄ MNPs) as an adsorbent for the removal of aniline. The characteristics of adsorbent were evaluated by SEM, TEM, XRD and BET. Also, the impact of different parameters such as pH, contact time, adsorbent dosage, aniline initials concentration and solution temperature were studied. The experimental data investigated by Langmuir and Freundlich adsorption isotherms and two models kinetically of pseudo first-order and pseudo second-order. The results indicated that the adsorption followed Langmuir and pseudo second-order models with correlation r² > 0.98 and r² > 0.99, respectively. The equilibrium time was obtained after 5 h. According to Langmuir model, the maximum adsorption capacity was 90.91 mg/g at pH = 6, and 20°C. The thermodynamic parameters indicated that adsorption of aniline on magnetic activated carbon was exothermic and spontaneous. This synthesized AC-Fe₃O₄ MNPs due to have advantages such as easy and rapid separation from solution could be applied as an adsorbent effective for removal of pollutants such as aniline from water and wastewater.