Challenges and effectiveness of nanotechnology-based photocatalysis for pesticides-contaminated water: A review.

Pesticides have been frequently used in agricultural fields. Due to the expeditious utilization of pesticides, their excessive usage has negative impacts on the natural environment and human health. This review discusses the successful implications of nanotechnology-based photocatalysis for the removal of environmental pesticide contaminants. Notably, various nanomaterials, including TiO2, ZnO, Fe2O3, nanoscale zero-valent iron, nanocomposite-based materials, have been proposed and have played a progressively essential role in wastewater treatment. In addition, a detailed review of the crucial reaction condition factors, including water matrix, pH, light source, temperature, flow rate (retention time), initial concentration of pesticides, a dosage of photocatalyst, and radical scavengers, is also highlighted. Additionally, the degradation pathway of pesticide mineralization is also elucidated. Finally, the challenges of technologies and the future of nanotechnology-based photocatalysis toward the photo-degradation of pesticides are thoroughly discussed. It is expected that those innovative extraordinary photocatalysts will significantly enhance the performance of pesticides degradation in the coming years.

Determination of Per- and Polyfluoroalkyl Substances in Craft Villages and Industrial Environments of Vietnam.

Per- and polyfluoroalkyl substances (PFASs) have attracted great concern because of their great recalcitrant nature and harmful environmental health effects. Eight PFASs in wastewater from craft villages and industrial environments of Vietnam were analyzed using liquid chromatography triple quadrupole mass spectrometry (LC-MS/MS) with negative electrospray ionization interface. For analysis of PFASs, percent recoveries ranged from 87 to 112, and MQL varied from 0.19 ng/L to 0.49 ng/L. Treated wastewater samples from eight metal-plating and eight textile-dyeing factories were collected for analysis of PFASs. Concentrations of PFOS in wastewater samples obtained from metal-plating factories with decorative plating stage were found at a range of 0.73-18.91 ng/L. For textile-dyeing factories, PFOA and/or PFHxA, which were present in all effluent wastewater samples, varied from 0.37 to 15.96 ng/L and 1.07 to 43.58 ng/L, respectively. Sixty surface water samples in four locations of the textile dyeing craft villages, a recycling plastic village, a paper recycling village, and 10 river water samples in the control area (a rural area without specific waste sources) were collected and analyzed for PFASs. The total concentrations of eight PFASs in surface water samples of craft villages ranged from 0.83 to 58.2 ng/L, which were significantly higher than those in the control area. PFOA, PFHxA, and PFOS are the three most dominant congeners in wastewater taken from craft villages with the highest concentrations of 27.4, 23.8, and 7.36 ng/L, respectively. The environmental risks posed by PFASs in surface water from craft villages were mainly in a range of extremely low to low level, particularly a few points have high ecological risks of PFDoA.

Occurrence, Distribution, and Ecological Risk Assessment of Antibiotics in Selected Urban Lakes of Hanoi, Vietnam.

Residue concentrations of fifteen antibiotics including sulfonamides, quinolones, macrolides, ß-lactams, and trimethoprim in lakes from Hanoi metropolitan area, Vietnam, were analyzed using ultra-performance liquid chromatography coupled with tandem mass spectrometry (UPLC/MS-MS) to elucidate their occurrence and behavior in urban environment. For surface water, the average concentrations of five antibiotic classes decreased in the order: sulfonamides (117.9 ng/L) > ß-lactams (31.28 ng/L) > quinolones (20.19 ng/L) > macrolides (17.74 ng/L) > trimethoprim (8.93 ng/L). While the highest concentration of SMX was detected at 806.5 ng/L in surface water, those obtained in sediment were only at 1.35 ng/g because of their high solubility in water. Quinolones were found at a maximal concentration of 158.7 ng/L for OFL in water phase whereas those in sediment phase were 4,017 ng/g due to their great affinity in sediment. These findings revealed the different fate and release mechanisms of each antibiotic group in the environment. The ecological risk assessment implied some targeted compounds, and in particular, OFL and AZM could pose high risks to algae in the aquatic ecosystem.

The degradation of paraben preservatives: Recent progress and sustainable approaches toward photocatalysis.

Parabens are a class of compounds primarily used as antimicrobial preservatives in pharmaceutical products, cosmetics, and foodstuff. Their widely used field leads to increasing concentrations detected in various environmental matrices like water, soil, and sludges, even detected in human tissue, blood, and milk. Treatment techniques, including chemical advanced oxidation, biological degradation, and physical adsorption processes, have been widely used to complete mineralization or to degrade parabens into less complicated byproducts. All kinds of processes were reviewed to give a completed picture of parabens removal. In light of these treatment techniques, advanced photocatalysis, which is emerging rapidly and widely as an economical, efficient, and environmentally-friendly technique, has received considerable attention. TiO2-based and non-TiO2-based photocatalysts play an essential role in parabens degradation. The effect of experimental parameters, such as the concentration of targeted parabens, concentration of photocatalyst, reaction time, and initial solution pH, even the presence of radical scavengers, are surveyed and compared from the literature. Some representative parabens such as methylparaben, propylparaben, and benzylparaben have been successfully studied the reaction pathways and their intermediates in their degradation process. As reported in the literature, the degradation of parabens involves the production of highly reactive species, mainly hydroxyl radicals. These reactive radicals would attack the paraben preservatives, break, and finally mineralize them into simpler inorganic and nontoxic molecules. Concluding perspectives on the challenges and opportunities for photocatalysis toward parabens remediation are also intensively highlighted.

Global challenges in microplastics: From fundamental understanding to advanced degradations toward sustainable strategies.

Currently, the global production and usage of plastics have increased rapidly with the expansion of synthetic polymers. Since plastics' degradation processes are prolonged and thus microplastics (MPs) potentially persist for very long periods in the environment. To date, there is a need for knowledge on the relevance of different potential entry pathways and the number of MPs entering the environment via different routes. Despite the vast quantity of studies that have been undertaken, many unanswered issues remain about the environmental impacts of MPs. The real impacts on a population subjected to many MPs of different structure, dimensions, and shapes over a lifetime are still hard to elucidate. Significantly, MPs can accumulate toxic substances, such as persistent organic pollutants, on their material surface. Hence, it represents a potential concentrated source of environmental pollution or acts as a vector of toxic pollutants in the food chain's interconnection with some severe health implications. Herein, we mainly discussed the global challenges in MPs, including the current production and use status of plastics and their impact on the environment. Additionally, finding the degradation of tiny fragment plastics (MPs level) is essential to remove plastics altogether. Some of the approaches to methods, including biodegradation, physical degradation, physicochemical degradation, have been successfully reviewed. More importantly, the sustainable concepts of using microorganisms and photocatalysis for MPs' degradation have been successfully proposed and demonstrated.

Optimization of sampling frequency for coastal seawater quality monitoring.

The selection of an appropriate sampling frequency is very important in monitoring coastal seawater quality. The present study sought to optimize the sampling frequency for coastal seawater quality monitoring. We combined mathematical models with natural and human activities by the analytic hierarchy process method. The study was designed to consider historical monitoring data, regulated seawater quality standard, tide, land use, and ship activities in optimizing coastal seawater sampling frequency in Ha Long Bay, Vietnam. The study results indicated that monitoring activities should focus in points having high human activities as well as high concentration of TSS, ammonium, and oil. Points S1-S8 should have high sampling frequency (16-30 samples/year), whereas points S23-S28 can have low sampling frequency (3-5 samples/year). In a year, monitoring activities should be focused in June, July, and August with the number of samples of 42, 54, and 44 pear year (weighting values 0.120, 0.161, and 0.112), respectively. It should consider the mathematical aspects associated with natural and human factors when calculating sampling frequency for coastal seawater quality monitoring. Proposed optimization method can be applied for other coastal regions.

Tailored photocatalysts and revealed reaction pathways for photodegradation of polycyclic aromatic hydrocarbons (PAHs) in water, soil and other sources.

Polycyclic aromatic hydrocarbons (PAHs), which are in the class of persistent organic pollutants, are considered as hazardous pollutants. To date, these compounds were detected globally in soil, sludge, water, and other contamination sources. A variety of treatment methods have been used in recent years to degrade PAHs in the environment. Photocatalysis, among advanced techniques, is proposed as the most effective method for the treatment of PAHs. In this context, we introduce the classification of PAHs, summarize, and highlight the recent studies on photodegradation of various types of PAHs. A series of efficient photocatalysts, including TiO2-, Ag3PO4-, ZnO-, MHCFs-based, and others, have been reported with the potential result for photodegradation of PAHs. Focus is also placed on revealing several possible reaction pathways for different types of PAHs that have been proposed in the literature. Particular attention to current status, challenges, and prospects in the future for enhanced photodegradation of PAHs are also discussed.

Polycyclic aromatic hydrocarbons (PAHs) in dry tea leaves and tea infusions in Vietnam: contamination levels and dietary risk assessment.

The total mean ∑[Formula: see text] in samples were from 75.3 to 387.0 ng/g dry weight (d.w) and showed high value in black dry tea, followed by herbal, oolong, and green tea. The mean ∑[Formula: see text] (a combination of benz[a]anthracene, chrysene, benzo[b]fluoranthene, and benzo[a]pyrene) values were 54.3 ng/g, 16.4 ng/g, 14.2 ng/g, and 6.6 ng/g for black, herbal, green, and oolong teas, respectively. Concentration for benzo[a]pyrene (BaP) was from 0.4 to 35.8 ng/g, and the BaP equivalent concentration values ranged from 0.3 to 48.1 ng/g. There was only 1 black tea sample that BaP concentration exceeded the maximum level according to European Union (EU) standards. Tea samples marketed in Vietnam showed insignificant difference with the samples from other origins by same analytical method. Black teas showed high PAHs contents in dry tea samples but the released percentage of sum of PAHs from tea-to-tea infusion was lower than that in other tea type samples. The released percentages of PAH4 from tea-to-tea infusion were 40.7, 15.4, and 1.9 for green, herbal, and black tea. High temperature in black tea manufacturing processes might reduce essential oil content in tea that might effect on the PAHs partially release into the infusion. Indeed, based on EU regulations, we may conclude that tea consumers are safe in risk of exposure to PAHs obtained from teas.

Enhancing decomposition rate of perfluorooctanoic acid by carbonate radical assisted sonochemical treatment.

Perfluorooctanoic acid (PFOA) is a recalcitrant organic pollutant in wastewater because of its wide range of applications. Technologies for PFOA treatment have recently been developed. In this study, PFOA decomposition by sonochemical treatment was investigated to determine the effects of NaHCO3 concentrations, N2 saturation, and pH on decomposition rates and defluorination efficiencies. The results showed that PFOA decomposition by ultrasound treatment only (150 W, 40 kHz), with or without saturated N2, was <25% after 4 h reaction. The extent and rate of PFOA decomposition and defluorination efficiencies of PFOA, however, greatly increased with the addition of carbonate radical reagents. PFOA was completely decomposed after 4h of sonochemical treatment with a carbonate radical oxidant and saturated N2. Without saturated N2, PFOA was also decomposed to a high (98.81%) degree. The highest PFOA decomposition and defluorination efficiencies occurred in N2 saturated solution containing an initial NaHCO3 concentration of 30 mM. Sonodecomposition of PFOA with CO3(-) radical was most favorable in a slightly alkaline environment (pH=8.65). There isn't any shorter-chain perfluorinated carboxylic acids detected except fluorine ions in final reaction solution.

Calculating of river water quality sampling frequency by the analytic hierarchy process (AHP).

River water quality sampling frequency is an important aspect of the river water quality monitoring network. A suitable sampling frequency for each station as well as for the whole network will provide a measure of the real water quality status for the water quality managers as well as the decision makers. The analytic hierarchy process (AHP) is an effective method for decision analysis and calculation of weighting factors based on multiple criteria to solve complicated problems. This study introduces a new procedure to design river water quality sampling frequency by applying the AHP. We introduce and combine weighting factors of variables with the relative weights of stations to select the sampling frequency for each station, monthly and yearly. The new procedure was applied for Jingmei and Xindian rivers, Taipei, Taiwan. The results showed that sampling frequency should be increased at high weighted stations while decreased at low weighted stations. In addition, a detailed monitoring plan for each station and each month could be scheduled from the output results. Finally, the study showed that the AHP is a suitable method to design a system for sampling frequency as it could combine multiple weights and multiple levels for stations and variables to calculate a final weight for stations, variables, and months.