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Many remediating strategies are used for polluted soils, however, but mostly the essential phytoremediation is a less expensive, organically satisfying technique that is generally reasonable for various countries. Pot tests were managed to dissect the Brassica júncea plant biomass cultivated on Pb as well as Cd polluted soils as well to survey its ampleness for the evacuation of Pb and Cd. Samples of picked plants developed at a blend of alluvial soil and sand were moved with vessel of pots the earth finishing extents as well allowed make with time regenerative development. Through acid digestion, Pb and Cd extraction was settled from the plant. Consequently, they were collected and afterwards examined for chosen metals through utilizing Atomic Absorption Spectrometry (AAS). Generally, the current examination results demonstrated that no hyperaccumulators of Pb as well Cd were recognized in the region. Body parts of the plant were categorized as Pb low accumulators, moderate accumulators and excluder, as well as Cd low accumulator, excluder. Additionally, Cd concentration was high up than the allowable range in species of plant. In plants, allowable range of Pb and Cd is 0.2 - 20 and 0.1 -2.4 mg kg – 1. In Brassica júncea plant the Pb as well Cd both were no hyperaccumulators. Hence, this local plant had the suitable ability to use for phytoremediation of contaminated soils around the Hayatabad Industrial area, Peshawar. All experimental Results demonstrated that from the medium of soil by Brassica júncea (L.) Czern plant the maximum lead and cadmium removals were 94 % and 94.26 %, respectively in the open environment, while in the control environment this removal was 82 % for Pb and 93.16 % for Cd .The present research work observes that brassica júncea (L.) Czern plant was more helpful for Cd take-up contrasted with Pb, and thus it is capacity we suggest Pb as well Cd for remediation from polluted soils. Keywords: Lead, Cadmium, Contaminated soil, Removal

This study focused on evaluating the use of powdered activated carbon (PAC) adsorption for the treatability of various odor compounds with different structures. The adsorption performance of 14 odor compounds under various PAC dosages were fitted with two isotherm models (the Langmuir and Freundlich models) to evaluate the adsorption ability. The results indicated that the adsorption capacities estimated from isotherm model predictions were not suitable for the evaluation of treatability of the odor compound due to the neglection of odor threshold. A novel assessment method, through the comparison of the residual concentration at an inflection point (where the downward trend of the odor compound residual concentration and PAC dosage curve starts to flatten) and the corresponding threshold concentration, was employed. This assessment method considered the different thresholds of the various odor compounds and their absorbability by PAC as well as the cost. The results indicated that only the sulfur odor compounds, including dimethyl disulfide, diethyl disulfide and dimethyl trisulfide, were not suitable for PAC treatment. Other odor compounds could be treated by PAC with varying success. The correlations between the adsorption capacity and the treatability of various odor compounds and their properties, including the coefficient between octanol and water (LogKw), solubility, molar refractivity (MR), dipole and volume, were also evaluated using the Pearson and Spearman correlation analysis. The results indicated that there were not significant correlations between the adsorption capacity and the properties of the odor compounds, while there were significant correlations between the treatability and LogKw, MR and volume. The odor causing compound with a larger LogKw, MR and volume was more suitable to be treated by PAC.

A new, environmental friendly, polysilicate ferric manganese (PSFM) coagulant, composed of Fe, Mn and Si, was designed and developed. As part of the process, the PSFM flocs were then deposited onto an ultrafiltration (UF) membrane to increase the removal of active dyes and its antifouling properties in the presence of the active dye was tested. Influencing factors, such as dosage of coagulant and solution pH, were systematically investigated and included as the process optimization. The results show that PSFM flocs were well distributed on the membrane surface and a dense and homogeneous deposition layer was formed under optimal conditions. According to the characterization of PSFM floc by Fourier infrared (FTIR) and X-ray photoelectron spectroscopy (XPS), the major phase of PSFM floc is determined to be Mn x Fe y Si z O w (OH) i and the functional groups of this component contribute positively to the coagulation performance. The removal rate of the active yellow dye reached 86% at pH 5.0 with small and regular floc formed in the dense deposition layers. At pH 11.0 loose deposition layers were formed by large flocs and the removal of the active yellow dye reduce to 11%. Therefore, PSFM has a commendable potential to be used for producing a kind of deposited UF membrane with an excellent performance by controlling the forms of flocs and the deposition layers, which is the key mechanism to achieve a high efficiency for removal of active yellow dye Refereed/Peer-reviewed

Protein, the main component of extracellular polymeric substances, plays a vital role in sediment dewatering. Tannic acid (TA) can bind with protein, so was used as a new conditioner for sediment dewatering. The benefit of using TA as a conditioner for sediment dewatering and its mechanism were explored in this study. A series of laboratory-based experiments were conducted and the water content (Wc) of sediment cakes, specific resistance to filtration (SRF) and the filterable dehydration rate were used to evaluate the sediment dewaterability. The results showed that at the optimal dosage of 0.20 mmol/gTS (total solid), TA reduced Wc of sediment cakes by 12.3% and SRF by 70.6%, and increased the filterable dehydration rate by 9%. These results indicated TA effectively improved the dewatering performance of sediment. The conditioning mechanism study of TA supported that the protein content was reduced by combining with TA, and the bound water was gradually converted into free water. When TA was added in sufficient amount, the particle size gradually increased, large and dense aggregates were formed which enhanced the dewatering performance of the sediment. These results confirm the feasibility of using TA as an effective option for rapid dewatering of sediment and provide a reference for selecting the appropriate conditioner for sediment dewatering. Refereed/Peer-reviewed

The color removal efficiencies by coagulation of two groups of laboratory-prepared dye solutions were compared; one group comprised dyes with the same chromophores and auxochromes, and the other group consisted of dyes with different chromophores and the same or different auxochromes. Several coagulants, polyaluminum chloride (PAC), cationic polyacrylamide (CPAM), anionic polyacrylamide (APAM), aluminum sulfate (alum as Al2(SO4)3), ferric chloride (FeCl3), aluminum chloride (AlCl3), and magnesium chloride (MgCl2), were selected to cover a large range of experimental variations in order to obtain sufficient data to predict and model the color removal efficiency. The effect of coagulant dosage on the color removal efficiency was determined, and the dye removal mechanism by coagulation was further investigated using the best performing coagulants for each dye group (disperse, acid, reactive, and basic). It was shown that the best dye–coagulant combinations that achieved superior color removal efficiency for each dye group with the same structures and functional groups were disperse dye–MgCl2 at a pH of 12, acid dye–MgCl2 at a pH of 12, reactive dye–PAC at a pH of 7.5, and basic dye–APAM at a pH of 8.3, in descending order. When treated with the same coagulant, dyes with the same auxochromes and charge exhibited very similar color removal efficiency. The state of the dye molecules in water was shown to have a significant influence on the coagulation effect. The experimental results indicated that the dye color removal efficiency by coagulation is a function of the dye structures. Refereed/Peer-reviewed

Due to the extensive existence of tetracyclines (TCs), struvite (MgNH4PO4·6H2O) recovery from swine wastewater will pose TCs-pharmacological threats to the agricultural planting and environment. This study investigated the influences of dissolved organic matters (DOM), as an important medium in the wastewater, on TCs transport during struvite recovery from swine wastewater. Compared to TCs concentrations of 1.49–2.16 μg/g in the solids obtained from synthetic wastewater, the existence of DOM significantly enhanced TCs contents in the products with the values of 360–742 μg/g. DOM was fractionated into four size fractions with different molecular weight cut-off, i.e. FDOM1 (30 kDa-0.45 μm), FDOM2 (5–30 kDa), FDOM3 (1–5 kDa) and FDOM4 (

The effects of coagulant dosage, alkalinity, turbidity, ionic strength, and dissolved organic matter (DOM) on the removal of sulfadimethoxazole (SMZ) and oxytetracycline (OTC) by coagulation were studied and the reaction mechanisms of the coagulation process were revealed in this research. From our results, alkalinity, turbidity, ionic strength, and DOM had different effects on the removal of antibiotics. The SMZ and OTC removals were improved with increase in poly-aluminum chloride (PACl) dosage, whereas the turbidity had less influence on the removal of SMZ and OTC because the adsorption of SMZ and OTC to kaolin was low, confirmed by a control when no PACl added. The hydrolysate of PACl played a more important role than turbidity in SMZ and OTC removals. The SMZ and OTC removals were significantly increased with the increase in alkalinity, which provided a suitable condition in situ for coagulant to form more optimal species of hydrolysate. The ionic strength, which was adjusted by NaNO3, also had a positive effect on the removal of SMZ but no obvious effect on the OTC removal. Furthermore, DOM had a higher effect on the removal of SMZ than that of OTC. In another word, if a water plant wants to improve the removal of SMZ and OTC by coagulation unit, PACl hydrolysate, alkalinity, and DOM are the three key factors to be considered primarily. Moreover, an experiment for the recovery of antibiotics from the flocs was done and the results showed that OTC and SMZ were removed by different mechanisms. The OTC was removed via complexation formed through the reaction between OTC and coagulant while the SMZ was removed through the pathway of adsorption and inter-particle bridging to the surface of coagulant hydrolysate Refereed/Peer-reviewed

Spatial and seasonal variations of arsenic species in Lake Taihu (including Zhushan Bay, Meiliang Bay, Gonghu Bay, and Southern Taihu) were investigated. Relatively high levels of total arsenic (TAs) and arsenate (As(V)) were observed in hyper-eutrophic regions during summer and autumn, which is attributed to exogenous contamination and seasonal endogenous release from sediments. The distributions of TAs and As(V) were significantly affected by total phosphorus, iron, manganese, and dissolved organic carbon. Arsenite (As(III)) and methylarsenicals (the sum of monomethylarsenic acid (MMA(V)) and dimethylarsenic acid (DMA(V))), mainly from biotransformation of As(V), were affected by temperature-controlled microalgae activities and local water quality parameters, exhibiting significantly higher concentrations and proportions in hyper-eutrophic and middle eutrophic regions during summer compared to mesotrophic region. The eutrophic environment, which induces changes in the main water quality parameters such as phosphorus, chlorophyll-a, iron, manganese, and dissolved organic carbon, can favor the biogeochemical cycling of arsenic in the aquatic systems.

Conventionally, resin fractionation (RF) method has been widely used to characterize dissolved organic matter (DOM) found in different source waters based on general and broad DOM fractions grouping. In this study, a new refined method using multistep, microvolume resin fractionation combined with excitation emission matrix fluorescence spectroscopy (MSM-RF-EEMS) was developed for further isolation and characterization of subfractions within the primary DOM fractions separated from using the conventional RF method. Subsequently, its feasibility in indicating the occurrence of urban pollution in source waters was also assessed. Results from using the new MSM-RF-EEMS method strongly illustrated that several organic subfractions still exist within the regarded primary pure hydrophobic acid (HoA) fraction including the humic- and fulvic-like organic matters, tryptophan- and tyrosine-like proteins. It was found that by using the MSM-RF-EEMS method, the organic subfractions present within the primary DOM fraction could be easily identified and characterized. Further validation on the HoA fraction using the MSM-RF-EEMS method revealed that the constant association of EEM peak T1 (tryptophan) fraction could specifically be used to indicate the occurrence of urban pollution in source water. The correlation analysis on the presence of EEM peak T2 (tyrosine) fraction could be used as a supplementary proof to further verify the presence of urban pollution in source waters. These findings on using the presence of EEM peaks T1 and T2 within the primary HoA fraction would be significant and useful for developing a sensory device for online water quality monitoring. Refereed/Peer-reviewed

The character of dissolved organic matter (DOM) in source waters from two countries (Australia and China) was investigated using an extended fractionation technique by combining resin adsorption, ultrafiltration and high performance size exclusion chromatography. There are distinctive chemical characteristics associated with DOM origins. Australian sourced DOM had higher hydrophobic acid (HoA) content and exhibited a more pronounced humic character, indicating a higher influence from allochthonous organics (decayed plant bodies from vegetated catchments). The higher content of hydrophobic base and neutral components found in Chinese DOM, may be attributed to the effects of increasing pollution caused by the rapid urbanization in China. The molecular weights (MWs) of aquatic HoA are predominantly in the moderate (e.g. 1–10 kDa) or small (e.g.

The pollutants in urban storm runoff, which lead to an non-point source contamination of water environment around cities, are of great concerns. The distributions of typical contaminants and the variations of their species in short term storm runoff from different land surfaces in Xiamen City were investigated. The concentrations of various contaminants, including organic matter, nutrients (i.e., N and P) and heavy metals, were significantly higher in parking lot and road runoff than those in roof and lawn runoff. The early runoff samples from traffic road and parking lot contained much high total nitrogen (TN 6–19 mg/L) and total phosphorus (TP 1–3 mg/L). A large proportion (around 60%) of TN existed as total dissolved nitrogen (TDN) species in most runoff. The percentage of TDN and the percentage of total dissolved phosphorus remained relatively stable during the rain events and did not decrease as dramatically as TN and TP. In addition, only parking lot and road runoff were contaminated by heavy metals, and both Pb (25–120 μg/L) and Zn (0.1–1.2 mg/L) were major heavy metals contaminating both runoff. Soluble Pb and Zn were predominantly existed as labile complex species (50%–99%), which may be adsorbed onto the surfaces of suspended particles and could be easily released out when pH decreased. This would have the great impact to the environment.

Dissolved organic matter (DOM) and its potential to form disinfection by-products (DBPs) during drinking water treatment raise challenges to water quality control. Understanding both chemical and physical characteristics of DOM in source waters is key to better water treatment. In this study, the DOM from four typical source waters in China was fractionated by XAD resin adsorption (RA) and ultrafiltration (UF) techniques. The trihalomethane formation potential (THMFP) of all fractions in the DOM were investigated to reveal the major THM precursors. The fraction distributions of DOM could be related to their geographical origins in a certain extent. The dominant chemical fraction as THM precursors in the DOM from south waters (East-Lake reservoir in Shenzhen and Peal rivers in Guangzhou) was hydrophobic acid (HoA). The size fraction with molecular weight (MW)

Urea hydrolysis has always been used to prepare alumina gels and little attention has been paid to the reactive polymeric Al species that is formed before alumina sol–gels occur. Based on the hydrolysis process of aluminum in urea solution at 90 °C, speciation and transformation of the reactive hydroxyl-Al polymers obtained by urea hydrolysis was investigated with Ferron assay, solution-state and solid-state 27Al NMR spectroscopy. Unlike the traditional viewpoint, Keggin-Al13 can form in solution without localized high alkalinity. The reaction of oligomers with Al(OH)4− resulted from the dissolving of colloidal Al hydroxides is accountable for the formation of Keggin-Al13. Alp1, the defected structure of Al13, was considered as the transient species in the transformation from Al13 to crystalline Al hydroxides. Besides Al13, some other reactive polymers with hexameric ring structure also exist. The two categories of Al species have different transformation models (i.e., forced hydrolysis and spontaneous hydrolysis). The forced hydrolysis model should be the main transformation pattern for Al species under the condition of strong base addition into Al solution. Sulphate ions inhibit the formation of high polymeric Al species and affect the crystal structure of the final Al precipitate.

Inorganic polymeric Al coagulants have been being widely used in water treatment due to their advantages of applicability within broad pH and temperature ranges, high capacity of charge neutralization as well as less alkalinity consumption. However, the removal of dissolved organic matter (DOM) by such kind of coagulants has not been well understood because of the complexity of natural organic matter and the diversity of such polymeric Al coagulants. In this paper, coagulants with different Al speciation characteristics were prepared to conduct coagulation of humic acid (HA). The humic acid used was peat origin and was characterized physicochemically. The results showed that coagulants with preformed Al species were less effective than conventional Al salt in removing humic acid with large molecular and hydrophobic properties. The floes formed by preformed Al species were smaller than those formed by conventional Al salt. Decreasing pH could improve the coagulation performance of all coagulants. Coagulation of humic acid might not follow the same charge neutralization rules associated with coagulation of mineral colloids. In the presence of humic acid, Al-13 could be decomposed during coagulation process. (c) 2006 Elsevier B.V. All rights reserved.

For pollution monitoring,we developed a new combined fractionation technique (CFT) to characterize dissolved organic matter (DOM) in natural water by combining resin adsorption (RA) and ultrafiltration (UF) with 3Dfluorescence measurement. We tested the new technique on 4 polluted and 4 unpolluted samples. The 3Dfluorescence characteristics of size sub-components in the hydrophobic acid (HPOA) fraction could distinguish unpolluted from polluted DOM. The unpolluted HPOA fraction was composed of a single dominant size component-peak A (fulvic-like, around Ex240/Em410 nm) material with relatively large molecular weight (MW) (>10 kDa). In comparison, the HPOA in polluted DOM contained another predominant size component with lower MW (

The application of a new combined fractionation technique (CFT) using high performance size exclusion chromatography (HPSEC) and rapid resin fractionation (RRF) for characterization of natural organic matter (NOM) in raw and post-coagulated water samples was assessed. Two natural water samples from Myponga and Hope Valley reservoirs, South Australia, respectively, were selected for this NOM removal by coagulation study. With the use of HPSEC and RRF individually, removal in the low molecular weight (LMW) organic region was observed by comparison of the HPSEC profiles of raw and treated waters and the removal of the hydrophobic organics was observed by comparing the RRF results. A new organic fractionation and characterization technique involving the sequential application of the two techniques, called RRF-HPSEC, was developed to provide additional analytical information particularly to determine the key control factor for the removal of LMW organics. The RRF-HPSEC results showed that good removal of LMW organics could be linked to the presence of high ratio of hydrophobic LMW organics compared with hydrophilic LMW organics. It was revealed, therefore, that the removal of LMW organics was achieved mainly through the reduction of hydrophobic fractions compared with hydrophilic fractions with the corresponding molecular weight. Refereed/Peer-reviewed

The pollutants in urban storm runoff, which lead to non-point source contamination of water environment around cities, are of great concerns. The distributions of typical contaminants and the variations of their species in short term storm runoff from different land surfaces in a seaside city in South China were investigated. The concentrations of various contaminants, including organic matter, nutrients (i.e., N and P) and heavy metals, were significantly higher in parking lot and road runoff than those in roof and lawn runoff. The early runoff samples from traffic road and parking lot contained much high total nitrogen (TN 6–19 mg/L) and total phosphorus (TP 1–3 mg/L). A large proportion (around 60%) of TN appeared as the species of total dissolved nitrogen (TDN) in most kinds of runoff. The percentage of TDN (%TDN) or percentage of total dissolved phosphorus (%TDP) remained relatively stable in runoff during the rain events and did not decrease as dramatically as TN or TP. In addition, only parking lot and road runoff were contaminated by heavy metals, in which only Pb (25–120 μg/L) and Zn (0.1–1.2 mg/L) were the significant heavy metal contaminants. Soluble Pb and Zn were predominantly existed as labile complex species (50%–99%), which are adsorbed on the surface of suspended particles and could be easily re-released out when ambient pH decreased. This indicates that the labile complex pb and Zn in urban runoff would have the largest impact on the aquatic environment.

Understanding the environmental safety and human health implications of engineered nanoparticles (ENPs) is of worldwide importance. As an important ENPs, engineered nano-TiO(2) (Enano-TiO(2)) may have been substantially deposited in aquatic sediments because of its widely uses. Sediment pore surface properties would be thus significantly influenced due to the large surface area of Enano-TiO(2). In this study, Enano-TiO(2) was found to greatly impact on sediment pore surface properties. The attachment of Enano-TiO(2) particles to sediment surfaces enhanced markedly BET specific surface area and t-Plot external specific surface area, and thereby increased sediment phosphorus (P) adsorption maximum (S(max)). Contrarily, the fill of Enano-TiO(2) particles into the micropores of sediments could significantly reduce t-Plot micropore specific surface area, and cause slight decrease in sediment P binding energy (K). Clearly, P sorbed in sediment would be easily released because of the decreasing P binding energy of the sediment with elevated Enano-TiO(2). Enano-TiO(2) would thus cause aggravated endogenous pollution in water if such sediment was re-suspended on disturbance. The results obtained in this study contribute to our increasing knowledge of how to regulate physicochemical behavior of pollutants in sediments under the influences of Enano-TiO(2) and/or similar ENPs.

Batch experiments were conducted to assess the effects of Cu(II) and Zn(II) on the biosorption of Pb(II) ions by fresh tissues of Myriophyllum spicatum. The biosorption of Pb(II) was examined for single, binary and ternary solutions at different initial concentrations and different pH values. The experimental results showed that the biosorption capacity increased with increasing pH from 2.0 to 6.0. Both Cu(II) and Zn(II) ions were found to have an adverse effect on the biosorption of Pb(II). The biosorption equilibrium data for single-metal solution were fitted to three isotherm models: Langmuir, Freundlich and Sips, and the Sips isotherm model gave the best fit for the experimental data. The maximum biosorption of Pb(II) in Pb–Cu binary system decreased with increasing concentration of copper ions, and the biosorption equilibrium data for the binary metal solution fitted the Langmuir competitive model well. Comparison between biosorption of Pb(II) and Cu(II) by M. spicatum in the binary solution could lead to the conclusion that the biosorbent (M. spicatum) has no preference of Pb(II) over Cu(II). Fourier transform infrared (FT-IR) spectroscopy was used to characterize the interaction between M. spicatum and Pb(II) ions. The results revealed that the carboxyl, hydroxyl and carbonyl groups are the main binding sites for Pb(II).

Iron oxides coated on Fe-0 core-shell nanospheres (nIOCl) were synthesized through the reduction of ferrous sulfate aqueous solution by sodium borohydride at ambient atmosphere. The catalyst was highly effective for the degradation of humic acid (HA) in the presence of H2O2 and UVA at neutral pH. Under deoxygenated conditions in the dark, the generation of hydroxyl radicals in aqueous nIOCl dispersion verified its galvanic cell-like performance, which enhanced the interfacial electron transfer and led to its higher reactivity. By the total organic carbon, the absorbance Of UV254, FTIR, the molecular weight distribution and the chemical fractional character analysis, the degradation process of HA was shown to proceed by the disappearance of aromaticity, the increase of hydrophilic fraction and aromatic ring openings into CO2 and small organic acid. The treated HA showed much lower reactivity toward chlorine and the disinfection byproduct (DBP) formation potential was also greatly reduced. Moreover, it was found that the DBP formation potential more depended on the structure of the intermediates of HA degradation than TOC removal. Crown Copyright (C) 2009 Published by Elsevier B.V. All rights reserved.

Characterizing natural organic matter (NOM), particles and elements in different water treatment processes can give a useful information to optimize water treatment operations. In this article, transformations of particles, metal elements and NOM in a pilot-scale water treatment plant were investigated by laser light granularity system, particle counter, glass-fiber membrane filtration, inductively coupled plasma-optical emission spectroscopy, ultra filtration and resin absorbents fractionation. The results showed that particles, NOM and trihalomethane formation precursors were removed synergistically by sequential treatment of different processes. Pre-ozonation markedly changed the polarity and molecular weight of NOM, and it could be conducive to the following coagulation process through destabilizing particles and colloids; mid-ozonation enhanced the subsequent granular activated carbon (GAC) filtration process by decreasing molecular weight of organic matters. Coagulation-flotation and GAC were more efficient in removing fixed suspended solids and larger particles; while sand-filtration was more efficient in removing volatile suspended solids and smaller particles. Flotation performed better than sedimentation in terms of particle and NOM removal. The type of coagulant could greatly affect the performance of coagulation-flotation. Pre-hydrolyzed composite coagulant (HPAC) was superior to FeCl3 concerning the removals of hydrophobic dissolved organic carbon and volatile suspended solids. The leakages of flocs from sand-filtration and microorganisms from GAC should be mitigated to ensure the reliability of the whole treatment system.

Dissolved organic matter (DOM) and its potential to form disinfection by-products (DBPs) during water treatment are of great public health concern. Understanding the seasonal changes in DOM composition and their reactivity in DBP formation could lead to a better treatment of drinking water and a more consistent water quality. DOM from the East-Lake, a reservoir in the south-China, was fractionated and characterized by XAD resin adsorption (RA) and ultrafiltration (UF) techniques during different seasons within a year. The properties of chemical fractions (isolated by RA) appeared more stable than those of physical fractions (separated by UF) throughout the sampling period. The relative contribution of each chemical fraction to the total dissolved organic carbon (DOC), UV254 absorbance and trihalomethane formation potential (THMFP) remained relatively constant across the sampling period. However, the physical (molecular weight) fractions of the DOM exhibited large seasonal changes in UV254 and THMFP. Compared to the parameter of DOC, the THMFP and specific THMFP (STHMFP) of either chemical or physical fractions were more variable. In terms of DOC concentration, the hydrophobic acids (HoA) and hydrophilic matter (HiM) dominated in the DOM in most of the seasons; while the components with molecular weight of 10-30 kDa and less than I kDa were the predominant physical fractions. (c) 2007 Published by Elsevier B.V.