Sonocatalytic degradation of tetracycline antibiotic using zinc oxide nanostructures loaded on nano-cellulose from waste straw as nanosonocatalyst.

The aim of the present investigation was the combination of ZnO nanostructures with nano-cellulose (NC) for the efficient degradation of tetracycline (TC) antibiotic under ultrasonic irradiation. The removal efficiency of 12.8% was obtained by the sole use of ultrasound (US), while the removal efficiency increased up to 70% by the US/ZnO treatment process. Due to the integration of ZnO nanostructures with NC, the removal efficiency of 87.6% was obtained within 45 min. The removal efficiency substantially decreased in the presence of tert-butyl alcohol (more than 25% reduction), indicating that radOH-mediation oxidation is responsible for the degradation of TC molecules. Peroxymonosulfate (PMS) led to the most enhancing effect on the removal of TC among percarbonate, persulfate and periodate ions. The addition of PMS caused the degradation efficiency of 96.4% within the short contact time of 15 min. The bio-toxicity examination on the basis of inhibition test conducted on activated sludge revealed diminishing the oxygen consumption inhibition percent [IOUR (%)] from 33.6 to 22.1% during the US/ZnO/NC process. Consequently, the utilization of the US/ZnO/NC process can convert TC molecules to less toxic compounds. However, longer reaction time is required for complete conversion into non-toxic substances.

Decomposition of ibuprofen in water via an electrochemical process with nano-sized carbon black-coated carbon cloth as oxygen-permeable cathode integrated with ultrasound.

The main aim of the present investigation was the treatment of ibuprofen (IBP)-polluted aquatic phase using a novel oxygen-permeable cathode (OPC)-equipped electrochemical process (ECP) integrated with ultrasound (US). According to kinetic modeling, the decomposition rate of IBP by the integrated process was 3.2 × 10-2 min-1 which was significant in comparison with the OPC-equipped ECP (1.4 × 10-2 min-1) and US alone (2.4 × 10-3 min-1). Increasing the current resulted in the enhanced generation of H2O2 and consequently, improved the degradation of IBP in the solution. Excessive concentrations of Na2SO4 as supporting electrolyte led to no significant enhancement in the reactor efficiency. At initial IBP concentration of 1 mg L-1, complete removal of IBP with reaction rate of 1.7 × 10-1 min-1 was happened within a short reaction time of 30 min. The pulse mode of US led to more than 10% increase in the removal efficiency compared with the normal mode. The presence of scavenging compound of methanol caused the highest drop in the efficiency of the integrated treatment process, indicating the substantial role of free hydroxyl radicals in the degradation of IBP. Intermediate byproducts generated in the solution during the decomposition were also identified and interpreted.

Implementation of martite nanoparticles prepared through planetary ball milling as a heterogeneous activator of oxone for degradation of tetracycline antibiotic: Ultrasound and peroxy-enhancement.

The aim of the present study was to employ martite nanoparticles synthesized through planetary ball milling instead of conventional sources of iron for the activation of Oxone in order to decompose tetracycline (TC) antibiotic in the aquatic phase. Accordingly, martite nanoparticles-activated Oxone exhibited a remarkable improvement in degrading TC molecules up to 87%. The results indicated an increased decomposition rate of TC with increasing Oxone concentration, martite nanoparticles dosage, and initial pH. In the absence of ultrasound, the decomposition rate of TC was 0.0481 min-1 within 30 min, while the implementation of ultrasound at 320 W and addition of hydrogen peroxide at 40 mM led to increase in the decomposition rate up to 0.0770 and 0.0907 min-1, respectively. The presence of carbonate and even persulfate ions suppressed the decomposition rate. Inversely, the addition of chloride and carbon tetrachloride enhanced the reactor performance in terms of TC degradation. Within four consecutive experimental runs, only 10.8% was dropped in the decomposition rate, indicating the appropriate reusability potential of martite nanoparticles. The results confirmed the appropriate ability of the treatment process in degrading and mineralizing the target pollutant but a longer exposure time is required for an efficient mineralization.

Sonocatalyzed decolorization of synthetic textile wastewater using sonochemically synthesized MgO nanostructures.

The present study focused on the synthesis of nanostructured MgO via sonochemical method and its application as sonocatalyst for the decolorization of Basic Red 46 (BR46) dye under ultrasonic irradiation. The sonocatalyst was characterized using X-ray diffraction (XRD) and field emission scanning electron microscopy (FE-SEM) equipped with energy dispersive X-ray microanalysis (EDX). In the following, the sonocatalytic removal of the dye under different operational conditions was evaluated kinetically on the basis of pseudo first-order kinetic model. The reaction rate of sonocatalyzed decolorization using MgO nanostructures (12.7 × 10(-3) min(-1)) was more efficient than that of ultrasound alone (2.0 × 10(-3) min(-1)). The increased sonocatalyst dosage showed better sonocatalytic activity but the application of excessive dosage should be avoided. The presence of periodate ions substantially increased the decolorization rate from 14.76 × 10(-3) to 33.4 × 10(-3) min(-1). Although the application of aeration favored the decolorization rate (17.8 × 10(-3) min(-1)), the addition of hydrogen peroxide resulted in a considerable decrease in the decolorization rate (9.5 × 10(-3) min(-1)) due to its scavenging effects at specific concentrations. Unlike alcoholic compounds, the addition of phenol had an insignificant scavenging effect on the sonocatalysis. A mineralization rate of 7.4 × 10(-3) min(-1) was obtained within 120 min. The intermediate byproducts were also detected using GC-MS analysis.