scholarly journals Complexation of Antimony with Natural Organic Matter: Performance Evaluation during Coagulation-Flocculation Process

Author(s):  
Muhammad Inam ◽  
Rizwan Khan ◽  
Du Park ◽  
Sarfaraz Khan ◽  
Ahmed Uddin ◽  
...  

The presence of natural organic matter (NOM) in drinking water sources can stabilize toxic antimony (Sb) species, thus enhancing their mobility and causing adverse effects on human health. Therefore, the present study aims to quantitatively explore the complexation of hydrophobic/hydrophilic NOM, i.e., humic acid (HA), salicylic acid (SA), and L-cysteine (L-cys), with Sb in water. In addition, the removal of Sb(III, V) species and total organic carbon (TOC) was evaluated with ferric chloride (FC) as a coagulant. The results showed a stronger binding affinity of hydrophobic HA as compared to hydrophilic NOM. The optimum FC dose required for Sb(V) removal was found to be higher than that for Sb(III), due to the higher complexation ability of hydrophobic NOM with antimonate than antimonite. TOC removal was found to be higher in hydrophobic ligands than hydrophilic ligands. The high concentration of hydrophobic molecules significantly suppresses the Sb adsorption onto Fe precipitates. An isotherm study suggested a stronger adsorption capacity for the hydrophobic ligand than the hydrophilic ligand. The binding of Sb to NOM in the presence of active Fe sites was significantly reduced, likely due to the adsorption of contaminants onto precipitated Fe. The results of flocs characteristics revealed that mechanisms such as oxidation, complexation, charge neutralization, and adsorption may be involved in the removal of Sb species from water. This study may provide new insights into the complexation behavior of Sb in NOM-laden water as well as the optimization of the coagulant dose during the water treatment process.

Author(s):  
Manoj Kumar Karnena ◽  
Madhavi Konni ◽  
Bhavya Kavitha Dwarapureddi ◽  
Vara Saritha

Abstract: One of the several significant concerns related to water treatment plants is the transformation of natural organic matter (NOM) concerning quality and quantity due to the changing climatic conditions. The NOM consists of heterogeneous functionalized groups. Phenolic and carboxyl groups are the dominant groups that are pH-dependent and show a stronger affinity towards the metals. Properties of natural organic matter and trace elements govern the binding kinetics, influencing cations' binding to functionalized groups at lower pH. The water treatment process mechanisms like adsorption, coagulation, membrane filtration, and ion exchange efficiencies are sturdily influenced by the presence of NOM with cations and by the natural organic matter alone. The complexation among the natural organic matter and coagulants enhances the removal of NOM from the coagulation processes. The current review illustrates detailed interactions between natural organic matter and the potential impacts of cations on NOM in the water and wastewater treatment facilities.


2013 ◽  
Vol 781-784 ◽  
pp. 1950-1953 ◽  
Author(s):  
Hong Tao Wang ◽  
Xue Bin Jia ◽  
Dong Mei Liu ◽  
Zhi Wei Wang ◽  
Yun Hao Pan

Source water polluted by algae, ammonium and organic matter has been studied for many years. Sudden pollution incidents of source water have been reported across the whole country. Seasonal variability of rainfall across China has resulted in floods or droughts, thus incurred the high concentration of algae, ammonium and organic matter, causing severe challenges to the conventional water purification facilities. However, the conventional water treatment process is often unavailable to keep the safety of source water for drinking when sudden pollution occurs. Meanwhile, byproducts are often to be found over the whole treatment process, it is high time that researchers took effective measures to deal with this problem. In the present work, an overview of the recent research dealing with source water suddenly polluted by algae, ammonium and organic matter is presented.


1992 ◽  
Vol 25 (7) ◽  
pp. 383-394 ◽  
Author(s):  
G. Garuti ◽  
M. Dohanyos ◽  
A. Tilche

Results of a three year experience on a combined anaerobic-anoxic-oxic municipal waste water treatment process - named ANANOX® - are presented. This process demonstrated to be highly efficient, with 89.6% CODt, 89.2% TSS and 81.2% N removal, and a sludge production of only 0.2 kg TSS.kg COD removed−1, a value which is roughly 50% less if compared with traditional nitrification/denitrification processes. Sulphates play a very significant role in the process because, after being reduced in the anaerobic step, where they give a contribution to the organic matter degradation, they are reoxidized in the anoxic step by nitrates, reducing the organic matter need for denitrification. Due to the high dependence of efficiency on temperature, the system proposed has advantageous uses for sewage treatment, particularly in warm climates and in tourist and recreational areas where the population increases during the warm season.


1990 ◽  
Vol 49 (3-4) ◽  
pp. 251-272 ◽  
Author(s):  
Oleh Weres ◽  
Harry R. Bowman ◽  
Aaron Goldstein ◽  
Emily C. Smith ◽  
Leon Tsao ◽  
...  

2020 ◽  
Vol 6 (1) ◽  
pp. 45-61 ◽  
Author(s):  
Paripurnanda Loganathan ◽  
Michael Gradzielski ◽  
Heriberto Bustamante ◽  
Saravanamuthu Vigneswaran

Natural organic matter (NOM) occurs ubiquitously in water bodies and this can greatly affect feed or raw water quality (taste, colour, odour, bacterial growth). Chemically modified chitosan can effectively remove NOM by the flocculation process.


Water ◽  
2019 ◽  
Vol 11 (4) ◽  
pp. 721 ◽  
Author(s):  
Lina Ramirez ◽  
Stephan Ramseier Gentile ◽  
Stéphane Zimmermann ◽  
Serge Stoll

Intensive use of engineered nanoparticles (NPs) in daily products ineluctably results in their release into aquatic systems and consequently into drinking water resources. Therefore, understanding NPs behavior in various waters from naturel to mineral waters is crucial for risk assessment evaluation and the efficient removal of NPs during the drinking water treatment process. In this study, the impact of relevant physicochemical parameters, such as pH, water hardness, and presence of natural organic matter (NOM) on the surface charge properties and aggregation abilities of both NPs and nanoplastic particles is investigated. TiO2, CeO2, and Polystyrene (PS) nanoplastics are selected, owing to their large number applications and contrasting characteristics at environmental pH. Experiments are performed in different water samples, including, ultrapure water, three bottled mineral waters, Lake Geneva, and drinking water produced from Lake Geneva. Our findings demonstrate that both water hardness and negatively charged natural organic matter concentrations, which were measured via dissolved organic carbon determination, are playing important roles. At environmental pH, when negatively charged nanoparticles are considered, specific cation adsorption is promoting aggregation so long as NOM concentration is limited. On the other hand, NOM adsorption is expected to be a key process in NPs destabilization when positively charged PS nanoplastics are considered.


1999 ◽  
Vol 40 (9) ◽  
pp. 157-163 ◽  
Author(s):  
Raymond M. Hozalski ◽  
Edward J. Bouwer ◽  
Sudha Goel

Removal of natural organic matter (NOM) in biofilters can be affected by many factors including NOM characteristics, use of pre-ozonation, water temperature, and biofilter backwashing. Laboratory experiments were performed and a biofilter simulation model was developed for the purpose of evaluating the effects of each of these factors on NOM removal in biofilters. Four sources of NOM were used in this study to represent a broad spectrum of NOM types that may be encountered in water treatment. In batch experiments with raw NOM, the removal of organic carbon by biodegradation was inversely proportional to the UV absorbance (254 nm)-to-TOC ratio and directly proportional to the percentage of low molecular weight material (as determined by ultrafiltration). The extent and rate of total organic carbon (TOC) removal typically increased as ozone dose increased, but the effects were highly dependent on NOM characteristics. NOM with a higher percentage of high molecular weight material experienced the greatest enhancement in biodegradability by ozonation. The performance of laboratory-scale continuous-flow biofilters was not significantly affected by periodic backwashing, because backwashing was unable to remove large amounts of biomass from the filter media. Model simulations confirmed our experimental results and the model was used to further evaluate the effects of temperature and backwashing on biofilter performance.


2002 ◽  
Vol 2 (5-6) ◽  
pp. 249-256 ◽  
Author(s):  
S. Wadley ◽  
T.D. Waite

The photo-Fenton process is becoming a practical treatment option for waters contaminated with pesticides and other organic compounds that are poorly biodegradable. This process can potentially be integrated into an existing water treatment process to enhance organic compound removal. It can operate at low concentrations of contaminant and can often completely mineralise the compound or convert it into a less toxic form. The process is most efficient at around pH 2.8; however, it has been found that with the addition of suitable complexing agents for Fe(III), the process can be operated at close to neutral pH. This study used citric acid as a complexing agent, 2,4-dichlorophenol (DCP) as a model contaminant and investigated the extension of the feasible pH range of the process from pH 5 to pH 8. The study involved synthetic solutions and light from a mercury arc lamp, with a bandpass filter used to isolate the emission band at around 360 nm. Low concentrations of DCP (12 μM) and Fe(II) (10 mM) were used to simulate conditions possible in the environment. In this work, no H2O2 was added, however, a relatively high concentration of citrate (100 μM) was used. Citrate is itself degraded in the process, and since it is highly biodegradable any excess could be consumed in a subsequent biological treatment process. The extent of degradation of DCP after 2 hours was found to be 91% at pH 5, 73% at pH 6, 74% at pH 7, and 59% at pH 8.


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