Microplastics, the microscopic plastics, are fragments of any type of plastic that are being produced today as plastic waste originating from anthropogenic activities. Such microplastics are discharged into the environment, and they enter back into the human body through different means. The microplastics spread in the environment due to environmental factors and the inherent properties of microplastics, such as density, hydrophobicity, and recalcitrance, and then eventually enter the water environment. In this study, to better understand the behavior of microplastics in the water environment, an extensive literature review was conducted on the occurrence of microplastics in aquatic environments categorized by seawater, wastewater, and freshwater. We summarized the abundance and distribution of microplastics in the water environment and studied the environmental factors affecting them in detail. In addition, focusing on the sampling and pretreatment processes that can limit the analysis results of microplastics, we discussed in depth the sampling methods, density separation, and organic matter digestion methods for each water environment. Finally, the potential hazards posed by the behavior of aging microplastics, such as adsorption of pollutants or ingestion by aquatic organisms, due to exposure to the environment were also investigated.

Undoped and Pr-doped ZnO nanoparticles were prepared using a simple sonochemical method, and their sonocatalytic activity was investigated toward degradation of Acid Red 17 (AR17) under ultrasonic (US) irradiation. Synthesized nanoparticles were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS) techniques. The extent of sonocatalytic degradation was higher compared with sonolysis alone. The decolorization efficiency of sonolysis alone, sonocatalysis with undoped ZnO and 5% Pr-doped ZnO was 24%, 46% and 100% within reaction time of 70min, respectively. Sonocatalytic degradation of AR17 increased with increasing the amount of dopant and catalyst dosage and decreasing initial dye concentration. Natural pH was favored the sonocatalytic degradation of AR17. With the addition of chloride, carbonate and sulfate as radical scavengers, the decolorization efficiency was decreased from 100% to 65%, 71% and 89% at the reaction time of 70min, respectively, indicating that the controlling mechanism of sonochemical degradation of AR17 is the free radicals (not pyrolysis). The addition of peroxydisulfate and hydrogen peroxide as enhancer improved the degradation efficiency from 79% to 85% and 93% at the reaction time of 50min, respectively. The result showed good reusability of the synthesized sonocatalyst.

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.

The present study was performed to sonochemically synthesize GdxZn₁-xO (x=0-0.1) nanoparticles for sonocatalysis of Acid Orange 7 (AO7) in an aqueous medium. The results of X-ray diffraction (XRD), scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FT-IR) and X-ray photoelectron spectroscopy (XPS) analysis confirmed proper synthesis of Gd-doped sonocatalyst. 5% Gd-doped ZnO nanoparticles with band gap of 2.8 eV exhibited the highest sonocatalytic decolorization efficiency of 90% at reaction time of 90 min. The effects of initial dye concentration and sonocatalyst dosage on decolorization efficiency were evaluated. In the presence of sodium sulfate, sodium carbonate and sodium chloride the decolorization efficiency decreased from 90 to 78, 65 and 56%, respectively. Among various enhancers, the addition of potassium periodate improved the decolorization efficiency from 90 to 100%. The highest decolorization efficiency was obtained at pH value of 6.34 (90%). The decolorization efficiency decreased only 6% after 4 repeated runs. Therefore, Gd-doped ZnO nanoparticles can be used as a promising catalyst for degradation of organic pollutants with great reusability potential.