Performance of conventional drinking water treatment following dispersant remediation of an oil spill in surface water

Author(s):  
Oluchi Okoro ◽  
Isabelle Papineau ◽  
Morgan Solliec ◽  
Louis Fradette ◽  
Benoit Barbeau
2001 ◽  
Vol 1 ◽  
pp. 39-43 ◽  
Author(s):  
V. Zitko

Many countries require the presence of free chlorine at about 0.1 mg/l in their drinking water supplies. For various reasons, such as cast-iron pipes or long residence times in the distribution system, free chlorine may decrease below detection limits. In such cases it is important to know whether or not the water was chlorinated or if nonchlorinated water entered the system by accident. Changes in UV spectra of natural organic matter in lakewater were used to assess qualitatively the degree of chlorination in the treatment to produce drinking water. The changes were more obvious in the first derivative spectra. In lakewater, the derivative spectra have a maximum at about 280 nm. This maximum shifts to longer wavelengths by up to 10 nm, decreases, and eventually disappears with an increasing dose of chlorine. The water treatment system was monitored by this technique for over 1 year and changes in the UV spectra of water samples were compared with experimental samples treated with known amounts of chlorine. The changes of the UV spectra with the concentration of added chlorine are presented. On several occasions, water, which received very little or no chlorination, may have entered the drinking water system. The results show that first derivative spectra are potentially a tool to determine, in the absence of residual chlorine, whether or not surface water was chlorinated during the treatment to produce potable water.


2013 ◽  
Vol 47 (11) ◽  
pp. 3591-3599 ◽  
Author(s):  
Zhang Can ◽  
Liu Wenjun ◽  
Sun Wen ◽  
Zhang Minglu ◽  
Qian Lingjia ◽  
...  

2020 ◽  
Vol 185 ◽  
pp. 109385 ◽  
Author(s):  
Donatella Feretti ◽  
Mattia Acito ◽  
Marco Dettori ◽  
Elisabetta Ceretti ◽  
Cristina Fatigoni ◽  
...  

2017 ◽  
Vol 23 (2) ◽  
pp. 328-337 ◽  
Author(s):  
Alessandra Imbrogno ◽  
Jennifer Biscarat ◽  
Andrea Iris Schafer

Background: Estrogens and their synthetic analogues are widely used as pharmaceuticals. Upon oral administration these drugs are eventually excreted via urine. The persistence of these pharmaceuticals and inefficient removal by water treatment lead to accumulation in surface water and effluents with negative effects for aquatic life and human health. Methods: In this study, the uptake of estradiol by a combined magnetic ion exchange resin - ultrafiltration process (MIEX-UF) was investigated. This is a relatively common process used in drinking water treatment for the removal of natural organic matter. However, uptake of micropollutants, such as steroidal pharmaceuticals, may occur as a side effect of water treatment due to the high affinity for polymeric materials. To elucidate the mechanism governing estradiol partitioning between water, resin and membrane, the influence of different parameters, such as pH, humic acid concentration and membrane molecular-weight-cut-off (MWCO) was studied. Results: Humic acid concentration and pH affected estradiol uptake most. At pH 11 the most significant increase of estradiol uptake was observed for MIEX-UF process (30 ng/g corresponding to 80%) compared with individual UF (17 ng/g corresponding to 12%). The presence of humic acid slightly reduced estradiol uptake at pH 11 (about 55%) due to competition for the ion exchange binding sites. Conclusion: Results demonstrated that the uptake of estradiol, which is amongst the most potent EDCs detected in surface water, in the MIEX-UF process can reach significant quantities (30 ng/g of resin) leading to uncontrolled accumulation of this micropollutant during drinking water treatment. This study gives a novel contribution in the understanding the mechanism of the unanticipated accumulation of pharmaceuticals, such as estradiol, in the drinking water treatment process.


2018 ◽  
Vol 217 ◽  
pp. 363-372 ◽  
Author(s):  
Changhui Wang ◽  
Yu Wu ◽  
Leilei Bai ◽  
Yaqian Zhao ◽  
Zaisheng Yan ◽  
...  

2006 ◽  
Vol 3 (6) ◽  
pp. 439 ◽  
Author(s):  
Martha J. M. Wells

Environmental Context. Worldwide, surface water is a source of drinking water and is a recipient of wastewater effluents and pollutants. Many surface water bodies undergo a natural, cyclical, diurnal variation in pH between 7 and 9. Most drinking water and wastewater treatment in the United States is conducted between pH 7 and 8. The pH of water undergoing treatment processes directly impacts the ratio of nonionized to ionized chemical form(s) present, which in turn impacts the success rate of contaminant removal. Many organic wastewater-derived contaminants are very water soluble at pH 7–8 and are inadequately treated. Abstract. Wastewater-derived contaminants (WWDCs) occur in surface water due to inadequate wastewater treatment and subsequently challenge the capabilities of drinking water treatment. Fundamental chemical properties must be understood to reduce the occurrence of known WWDCs and to better anticipate future chemical contaminants of concern to water supplies. To date, examination of the fundamental properties of WWDCs in surface water appears to be completely lacking or inappropriately applied. In this research, the hydrophobicity–ionogenicity profiles of WWDCs reported to occur in surface water were investigated, concentrating primarily on pharmaceuticals and personal care products (PPCPs), steroids, and hormones. Because most water treatment is conducted between pH 7 and 8 and because DOW, the pH-dependent n-octanol–water distribution ratio embodies simultaneously the concepts of hydrophobicity and ionogenicity, DOW at pH 7–8 is presented as an appropriate physicochemical parameter for understanding and regulating water treatment. Although the pH-dependent chemical character of hydrophobicity is not new science, this concept is insufficiently appreciated by scientists, engineers, and practitioners currently engaged in chemical assessment. The extremely hydrophilic character of many WWDCs at pH 7–8, indicated by DOW (the combination of KOW and pKa) not by KOW of the neutral chemical, is proposed as an indicator of occurrence in surface water.


2020 ◽  
Vol 4 ◽  
pp. 56
Author(s):  
Colin Hendrickson ◽  
Jared Oremo ◽  
Oscar Oluoch Akello ◽  
Simon Bunde ◽  
Isaac Rayola ◽  
...  

 Background: Decentralized drinking water treatment methods generally apply membrane-based treatment approaches. Ozonation of drinking water, which previously has only been possible at large centralized facilities, can now be accomplished on a small-scale using microplasma technology. The efficacy of decentralized solar-powered drinking water treatment systems has not previously been described. Methods: We established a 1,000L decentralized solar-powered water treatment system located in Kisumu County, Kenya. Highly contaminated surface water is pumped to the treatment system, which includes flocculation and filtration steps prior to ozonation. Turbidity, total coliform bacteria, and E. coli were measured at various stages of water treatment, and bacterial log reduction values (LRVs) were calculated. Results: Forty-seven trials were conducted in which1000L of water were flocculated, filtered, and ozonated for 180 minutes. Baseline turbidity and E. coli concentrations were reduced from a median of 238 nephelometric turbidity units (NTU) and 2,419.7 most probable number/100mL, respectively, in surface water to 1.0 NTU and undetectable E. coli after ozonation for 180 minutes. The median E. coli LRV was 3.99. Conclusions: The solar-powered, decentralized water treatment system that utilizes ozonation for disinfection was founded to reduce E. coli by more than 3 log-orders of magnitude despite the high turbidity of the raw water. Further research is needed to characterize limitations, scalability, economic viability, and community perspectives that could help determine the role for similar systems in other settings.


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