Review of pollutants removed by electrocoagulation and electrocoagulation/flotation processes

The word “electrocoagulation” (EC) will be sometimes used with “electroflotation” (EF) and can be considered as the electrocoagulation/flotation (ECF) process. Through the process of electrolysis, coagulating agents such as metal hydroxides are produced. When aluminium electrodes are used, the aluminium dissolves at the anode and hydrogen gas is released at the cathode. The coagulating agent combines with the pollutants to form large size flocs. As the bubbles rise to the top of the tank they adhere to particles suspended in the water and float them to the surface. In fact, a conceptual framework of the overall ECF process is linked to coagulant generation, pollutant aggregation, and pollutant removal by flotation and settling when it has been applied efficiently to various water and wastewater treatment processes. This review paper considers a significant number of common applications of EC and ECF processes which have been published in journal and conference papers.     

Assessment of intrinsic vulnerability to contamination for Gaza coastal aquifer, Palestine

Gaza coastal aquifer (GCA) is the major source of fresh water for the 1.5 million residents of Gaza Strip, Palestine. The aquifer is under deteriorating quality conditions mainly due to the excessive application of fertilizers. The intrinsic vulnerability of GCA to contamination was assessed using the well-known DRASTIC method. Detailed analysis of the intrinsic vulnerability map of GCA was carried out and did consider different relationships between the vulnerability indices and the on-ground nitrogen loadings and land use classes. In addition, correlation between vulnerability values and the nitrate concentrations in GCA was studied. Based on the vulnerability analysis, it was found that 10% and 13% of Gaza Strip area is under low and high vulnerability of groundwater contamination, respectively, while more than 77% of the area of Gaza Strip can be designated as an area of moderate vulnerability of groundwater contamination. It was found that the density of groundwater sampling wells for nitrate concentration is high for the moderate and high vulnerability zones. The highest first quartile, median, mean, and third quartile of nitrate concentrations are reported in the high vulnerability zones. Results of sensitivity analysis show a high sensitivity of the high vulnerability index to the depth to water table.     

Seasonal differences in treatment efficiency of a set of stabilization ponds in a semi-arid region

This article aims to determine the significant differences of the seasonal changes of pH, chemical oxygen demand (COD), biological oxygen demand (BOD), and total suspended solids (TSS) parameters in a wastewater stabilization pond. The variation of these parameters followed the seasonal pattern of temperature. The mean seasonal pH of the influent wastewater ranged between 7.8 (in spring) and 7.9 (in summer), while in the final effluents it was between 7.9 (in winter) and 8.3 (in summer). The mean seasonal COD of the influent wastewater ranged between 650?mg?L^?1 in spring and 600?mg?L^?1 in autumn, whereas in the effluents it was between 150?mg?L^?1 in autumn and 270?mg?L^?1 in spring. The mean seasonal BOD₅ of the influent wastewater ranged between 360?mg?L^?1 in autumn and 390?mg?L^?1 in winter, whereas in the effluents it was between 66?mg?L^?1 in summer and 130?mg?L^?1 in winter. The results showed that the percent removals of COD, BOD₅ and TSS from final effluents were maximum in summer for COD and BOD₅ (76%), summer (83%) and for TSS in winter (78%), respectively. Data analysis showed that there were significant differences between parameters of pH, COD, BOD₅ and TSS at four different seasons (p?相似文献   

Perfluoroalkane acids in human milk under the global monitoring plan of the Stockholm Convention on Persistent Organic Pollutants (2008–2019)

● Perfluorooctanesulfonic acid and perfluorooctanoic acid highest in human milk. ● All other perfluoroalkane substances had median values of zero (101 samples). ● Branched PFOS recommended to be analyzed separately from linear isomer. ● PFOS and PFOA showed differentiated regional and income distribution. ● Human health risk assessment values not yet available at global level. Within the global monitoring plan (GMP) established by article 16 of the Stockholm Convention on Persistent Organic Pollutants, perfluorooctane sulfonic acid (PFOS), perfluorooctanoic acid (PFOA), and perfluorohexane sulfonic acid (PFHxS) are recommended for analysis in core matrices to assess occurrence and changes geographically and with time. In 101 samples consisting of 86 national pools and 15 pools from States in Brazil obtained between 2008 and 2019, PFHxS was detected in 17% of the national pools and none in Brazil. PFOA and PFOS had a detection frequency of 100% and 92%, respectively. Other perfluoroalkane substances (PFAS) had either low detection frequencies and median values of zero (carboxylic acids C₄–C₁₁; except PFOA) or could not be quantified in any sample (sulfonic acids, C₄–C₁₀, and long-chain carboxylic acids, C₁₂–C₁₄). Correlation between PFOA and PFOS was moderately (r = 0.58). Whereas median values were almost identical (18.9 pg/g f.w. for PFOS; 18.6 pg/g f.w. for PFOA), PFOS showed larger ranges (< 6.2 pg/g f.w.–212 pg/g f.w.) than PFOA (< 6.2 pg/g f.w.–63.4 pg/g f.w.). It was shown that wealthier countries had higher PFOA concentrations than poorer countries. No difference in concentrations was found for samples collected in countries having or not having ratified the Stockholm Convention amendments to list PFOS or PFOA. The goal to achieve 50% decrease in concentrations within ten years was met by Antigua and Barbuda, Kenya, and Nigeria for PFOS and by Antigua and Barbuda for PFOA. In a few cases, increases were observed; one country for PFOS, four countries for PFOA.     

Combined UV-C/H2O2-VUV processes for the treatment of an actual slaughterhouse wastewater

In this study, a three-factor, three-level Box-Behnken design with response surface methodology were used to maximize the TOC removal and minimize the H₂O₂ residual in the effluent of the combined UV-C/H₂O₂-VUV system for the treatment of an actual slaughterhouse wastewater (SWW) collected from one of the meat processing plants in Ontario, Canada. The irradiation time and the initial concentrations of total organic carbon (TOC_o) and hydrogen peroxide (H₂O_2o) were the three predictors, as independent variables, studied in the design of experiments. The multiple response approach was used to obtain desirability response surfaces at the optimum factor settings. Subsequently, the optimum conditions to achieve the maximum percentage TOC removal of 46.19% and minimum H₂O₂ residual of 1.05% were TOC_o of 213 mg L^?1, H₂O_2o of 450 mg L^?1, and irradiation time of 9 min. The attained optimal operating conditions were validated with a complementary test. Consequently, the TOC removal of 45.68% and H₂O₂ residual of 1.03% were achieved experimentally, confirming the statistical model reliability. Three individual processes, VUV alone, VUV/H₂O₂, and UV-C/H₂O₂, were also evaluated to compare their performance for the treatment of the actual SWW using the optimum parameters obtained in combined UV-C/H₂O₂-VUV processes. Results confirmed that an adequate combination of the UV-C/H₂O₂-VUV processes is essential for an optimized TOC removal and H₂O₂ residual. Finally, respirometry analyses were also performed to evaluate the biodegradability of the SWW and the BOD removal efficiency of the combined UV-C/H₂O₂-VUV processes.     

Currently used organophosphate and brominated flame retardants in the environment of China and other developing countries (2000–2016)

This review summarizes the environmental occurrence of new brominated flame retardants (NBFRs) and organophosphate compounds (OPs) in the environment of developing countries since 2000. The ban on the production and use of commercial formulations of polybrominated diphenyl ethers (PBDEs) have paved the way for the high use of NBFRs and OPs in consumer products to fulfill the fire safety regulations. Recent studies have shown that the ever increasing production volumes and extensive use of these chemicals as additive FRs and plasticizers have resulted into their ubiquitous occurrence in all environmental compartments. Although presumed to be safe for use and the environment, recent studies on their occurrence and persistence in the environment have raised questions. Due to the lack of awareness, research interest, and availability of technical facilities, limited scientific data is available on the occurrence of these chemicals in developing countries. In this study, we collected reported data and provide an overview of environmental occurrence of NBFRs and OPs in abiotic and biotic matrices of different developing countries. Finally, research gaps were identified with recommendations for future research work and would be useful towards the environmental management of these toxic chemicals.