Occurrence, distribution and sources of phthalates and petroleum hydrocarbons in tropical estuarine sediments (Mandovi and Ashtamudi) of western Peninsular India.

The present study provides baseline information on the concentration levels, distribution characteristics and pollution sources of environmental contaminants, such as phthalic acid esters (PAEs or phthalates) and petroleum hydrocarbons in surface sediments of the tropical estuaries (Mandovi and Ashtamudi) from western Peninsular India. Total PAEs (∑5PAEs), hopanes, steranes and diasteranes concentrations from Ashtamudi estuary ranged from 7.77 to 1478.2 ng/g, n.d.-363.2 ng/g, n.d.-121.5 ng/g and n.d.-116.6 ng/g, respectively. Likewise, PAEs (∑6PAEs), steranes and diasteranes concentrations from Mandovi estuary ranged from 60.1 to 271.9 ng/g, 2.33-40.1 ng/g and 2.28-23.0 ng/g, respectively. The PAEs comprising di-isobutyl phthalate (DIBP), dibutyl phthalate (DBP), an isomer peak for DBP, di(2-ethylhexyl) phthalate (DEHP), di-isononyl phthalate were dominant in Ashtamudi estuary sediments, while PAEs including diethyl phthalate, DIBP, DBP and its isomer, DEHP, di(2-ethylhexyl) terephthalate were detected in the Mandovi sediment samples. The results of this study show an insignificant correlation of TOC with PAEs, and indicates that the varying spatial distributions of the PAEs in both the estuaries can be the result of discharge sources. The higher concentration of PAE congeners was noticed in Ashtamudi, a Ramsar wetland site, that can be attributed to land-based plastic waste. The petroleum biomarkers were abundantly present in Mandovi estuary due to anthropogenic activities such as boating and spillage from oil tankers. The findings of the present study will serve as a reference point for future investigation of organic contaminants in Indian estuaries, and calls for attention towards implementing effective measures in controlling the pervasion of the PAEs and petroleum biomarkers.

[Validation Study on Developed Methods for Total Organic Carbon in Some Kinds of Mineral Water].

Total organic carbon (TOC) was measured in some kinds of mineral water, and the method was validated. In mineral water, there are many kinds of elements such as carbon dioxide and a wide range of hardness. The official method for amount of TOC in tap water was validated in non-carbonated mineral water regardless of the degree of hardness. However, the amount of TOC was not accurately measured in two kinds of carbonated mineral water with medium or high degree of hardness. In our method of this study, the removal of carbon dioxide from the two kinds of mineral water was achieved by making bubbling time longer and additive rate of HCl upper than the official condition of tap water. And then, the method we developed was validated in the two kinds of mineral water. Our results suggested that the method we developed could be useful to measure the amount of TOC in many kinds of mineral water on the market.

Determination of Synthetic Musks in Sediments of Yellow River Delta Wetland, China.

In this study, seven kinds of synthetic musks were characterized in sediment samples of Yellow River Delta wetland, including celestolide, phantolide, traseolide, galaxolide, tonalide, musk xylene, and musk ketone. They were analyzed using gas chromatography-mass spectrometry (GC-MS), with recoveries of 91.85 %-105.35 % and the relative standard deviation (% RSD) were 3.30 %-8.11 % for all analytes. Galaxolide and tonalide were the main musk contaminants which were detected in sediment samples. The total concentrations of galaxolide ranged from 1.42 to 8.60 ng/g (mean 2.92 ng/g) (dry weight, dw); the total concentrations of tonalide ranged from the detection limit (LOD) to 3.63 ng/g (mean 1.69 ng/g, dw). The one reason of the higher level of SM pollutants was the domestic wastewater dumped by the local residents in some sites. And there was no significant correlation between SMs and TOC in sediment samples of Yellow River Delta wetland (p > 0.05).

Mo-BiVO4 Photocatalytically Modified Ceramic Ultrafiltration Membranes for Enhanced Water Treatment Efficiency.

This study highlights the effectiveness of photocatalytically modified ceramic ultrafiltration (UF) membranes in alleviating two major drawbacks of membrane filtration technologies. These are the generation of a highly concentrated retentate effluent as a waste stream and the gradual degradation of the water flux through the membrane due to the accumulation of organic pollutants on its surface. The development of two types of novel tubular membranes, featuring photocatalytic Mo-BiVO4 inverse opal coatings, demonstrated a negligible impact on water permeance, ensuring consistent filtration and photocatalytic efficiency and suggesting the potential for maintaining membrane integrity and avoiding the formation of highly concentrated retentate effluents. Morphological analysis revealed well-defined coatings with ordered domains and interconnected macropores, confirming successful synthesis of Mo-BiVO4. Raman spectroscopy and optical studies further elucidated the composition and light absorption properties of the coatings, particularly within the visible region, which is vital for photocatalysis driven by vis-light. Evaluation of the tetracycline removal efficiency presented efficient adsorption onto membrane surfaces with enhanced photocatalytic activity observed under both UV and vis-light. Additionally, vis-light irradiation facilitated significant degradation, showcasing the versatility of the membranes. Total Organic Carbon (TOC) analysis corroborated complete solute elimination or photocatalytic degradation without the production of intermediates, highlighting the potential for complete pollutant removal. Overall, these findings emphasize the promising applications of Mo-BiVO4 photocatalytic membranes in sustainable water treatment and wastewater remediation processes, laying the groundwork for further optimization and scalability in practical water treatment systems.

Selected pesticidal POPs and metabolites in the soil of five Vietnamese cities: Sources, fate, and health risk implications.

Large quantities of organochlorine pesticides (OCPs) have been used in tropical regions. The fate processes and risks of these legacy contaminants in the tropics are poorly understood. Herein, we investigated the occurrence of three classes of widely used OCPs and their metabolites in surface and core soil from five cities across Vietnam with a prevalent tropical monsoon climate and a long history of OCP application. We aimed to elucidate migration potentials, degradation conditions, and transformation pathways and assess current health risks of these contaminants. Generally, the concentrations of OCPs and metabolites in the soil core were slightly lower than those in surface soil except for hexachlorocyclohexane (HCH) isomers. 2,2-bis(4-chlorophenyl)-1,1,1-trichloroethane (p,p'-DDT), 2,2-bis(4-chlorophenyl)-1,1-dichloroethylene (p,p'-DDE), the sum of dicofol and 4,4'-dichlorobenzophenone (p,p'-DBP), and 2,2-bis(4-chlorophenyl)-1,1-dichloroethane (p,p'-DDD) were the most abundant compounds in both surface and core soils. A uniform distribution of HCHs (the sum of α-, ß-, γ-, and δ-HCH) at trace levels was found in almost all soils, serving as evidence of the lack of recent use of HCH pesticides. Higher concentrations of DDTs (the sum of DDT, DDD, and DDE) were observed in north-central Vietnamese soil, whereas appreciable concentrations of ENDs (the sum of α- and ß-endosulfan and endosulfan sulfate) were only found in southern Vietnamese soils. Empirical diagnostic ratios indicated residuals of DDTs were mainly from technical DDT rather than dicofol, whereas aged HCHs could be explained by the mixture of lindane and technical HCH. Both historical applications and recent input explain DDTs and ENDs in Vietnamese soil. Total organic carbon performs well in preventing vertical migration of more hydrophobic DDTs and ENDs. The dominant transformation pathway of DDT in surface soil followed p,p'-DDE→2,2-bis(4-chlorophenyl)-1-chloroethylene or p,p'-DDMU→1,1-bis(4-chlorophenyl)ethylene or p,p'-DDNU→p,p'-DBP, whereas the amount of p,p'-DDMU converted from p,p'-DDD and p,p'-DDE is similar in soil core. Non-cancer risks of OCPs and metabolites in all soils and cancer risks of those chemicals in core soils were below the safety threshold, whereas a small proportion of surface soil exhibited potential cancer risk after considering the exposure pathway of vegetable intake. This study implied that organic matter in non-rainforest tropical deep soils still could hinder the leaching of hydrophobic organic contaminants as in subtropical and temperate soils. When lands with a history of OCP application are used for agricultural purposes, dietary-related risks need to be carefully assessed.

Removal of As(III)/As(V) from aqueous solution using newly developed thiosalicylic acid coated magnetite [TSA@Fe3O4] nanoparticles.

The aim of this study was to develop an affordable adsorption methodology for removal of As(III)/As(V) from contaminated water. Herein, novel adsorbent TSA@Fe3O4 nanoparticles (NPs) were synthesized by decorating thiosalicylic acid (TSA) on magnetite nanoparticles (Fe3O4 NPs) and employed for removal of As(III)/As(V) species from artificially contaminated natural water systems. TSA@Fe3O4 NPs demonstrated excellent adsorption efficiency (AE) and 98% of As(V) and 93% of As(III) was removed at optimized experimental conditions. The adsorption kinetic and equilibrium isotherm studies were conducted preferentially for As(III) adsorption. Adsorption followed the pseudo-second-order kinetic (R2 = 99%) and adsorption data fitted well in Langmuir isotherm model (R2 = 99%) and maximum adsorption capacity (Qmax = 34.1 mg/g) was calculated for 5 mg/L of As(III) by using 10 mg of TSA@Fe3O4 NPs. The effect of pH, contact time, adsorption dosages, and competitive anions was also examined to identify optimum experimental conditions. The adsorbent was characterized by advanced instrumental techniques to investigate the physicochemical properties and stability of NPs. To comprehend the interactions of As(III) species with adsorbent NPs, NPs were analyzed using XPS and Raman spectroscopy techniques. Both the techniques confirmed that As(III) and As(V) species present simultaneously on adsorbent surface. The TSA@Fe3O4 was regenerated using 0.1 M NaOH. The findings of this study suggested that TSA@Fe3O4 NPs could be considered a potential adsorbent for effective remediation of As(III) and As(V) from contaminated natural water systems.

Heavy metals in the sediments of Laoshan Bay, China: Distribution and contamination assessment.

We analyzed total organic carbon (TOC), total nitrogen (TN), and heavy metals in 58 sediment samples from the Laoshan Bay, China. TOC and TN results identified marine primary production as the dominant source for organic matter, and the weak correlations between TOC, TN, and heavy metals indicated the terrestrial origin of heavy metals. Cd showed insignificant correlations with other metals, which suggests that agriculture production is the main anthropogenic activity affecting the distribution of Cd. Pb contamination in past 50 years was likely to have occurred because of fossil fuel combustion. Despite 210Pb dating, it was still difficult to trace the contamination condition over interannual variations. Nonetheless, these results provide data for monitoring Pb contamination. As Laoshan Bay is an important economic area, it would be beneficial to conduct further studies to determine the sources and degree of contamination for each heavy metal.

[Distribution of Typical Pollutants from Rainwater Sewer Sediments in Suzhou City].

In this study, we separately collected rainwater sewer sediments from typical samples in Suzhou city, such as the urban commercial district, historical and cultural protection area, cultural and educational area, and living area, and analyzed the particle size distribution of the sediments and the characteristics of carbon, nitrogen, phosphorus content, and pollution load distribution under each graded particle size. The median particle size D50 of each sample point was 16.55-327.50 µm, and the particle size trend was as follows:commercial area > living area > historical and cultural protection area > cultural and educational area. D50 was related to the total organic carbon (TOC). The total nitrogen (TN), total phosphorus (TP), and ammonia nitrogen (NH4+-N) were significantly positively correlated, as were the pollutants. The spatial difference of ω(TOC), ω(TN), ω(TP), and ω(NH4+-N) in rainwater sewer sediments from different regions was as follows:commercial area > historical and cultural protection area > living area > cultural and educational area, in which ω(TOC) was 0.84%-6.76%, and ω(TN), ω(TP), and ω(NH4+-N) were 917.5-12707.1, 196.1-2524.8, and 9.3-156.8 mg·kg-1, respectively. TOC, TP, and NH4+-N pollution loads were mainly concentrated on particles ≤ 75 µm and 250-1000 µm. Street dust pollutants highly differed spatially, with a high content of attached pollutants on street dust particles with a particle size of ≤ 75 µm. Various pollutants migrated into the street dust-pipes, and TP and TN showed certain enrichment characteristics in the sewer. Controlling the transportation of street dust and the accumulation of sediments in the sewer can reduce the pollution of sediment into the rivers during the rainy season.

Rinsing Recommendations for Membrane Filters and Identification of Rinsables.

Filtration is universally used in biopharmaceutical processing. For example, in upstream processing for sterilizing-grade filtration of cell culture media or in various downstream operations, such as clarification, filtration of intermediates, and in critical final filling applications. It is well known that filtration devices can release a certain level of organic compounds within the first filtrate fractions, which can be measured as total organic carbon (TOC). The compounds are primarily released from the surface of its construction materials. This includes typical polymer constituents that migrate from the material, as well as compounds which are formed during sterilization by irradiation. The level of compounds present on a surface is reduced significantly during rinsing of filters. Therefore, these can be defined as "rinsables". A deeper understanding of filter rinsing characteristics and chemical composition of a rinse solution is relevant for process design and risk mitigation, especially in high-risk applications. This publication provides the analytical and mathematical tools to measure and evaluate rinsing curves obtained from different sterilizing-grade membrane filter capsules. Total organic carbon (TOC) content, high-resolution mass spectrometry, ion chromatography, and headspace GC-MS were used to determine the composition of rinsing fractions and to follow the course of the rinsing curve. The required, filter-specific parameters Bulk Volume per Surface area (BVS) and Rinsing Volume per Surface area (RVS) are introduced. They are used for calculating minimum bulk and rinsing volumes of filters that lead to TOC concentrations below the threshold of 500 µg/L for Water for Injection. Three relevant filtration cases in biopharmaceutical manufacturing are discussed together with best practices for evaluation and use of BVS and RVS parameters. Results of a verification test are presented and discussed.

Land-use and climate controls on aquatic carbon cycling and phototrophs in karst lakes of southwest China.

Land-use and climate changes have been repeatedly identified as important factors affecting terrestrial carbon budgets, however little is known about how deforestation and catchment development affect aquatic systems in carbonate-rich regions. Multi-proxy analyses of 210Pb-dated sediment cores from two hard-water lakes with different land-use histories were applied for assessing carbon cycling and limnological changes in response to land-use changes over the past century in southwest China. Logging of primary forests in the catchment of Lugu Lake, starting in the 1950s, led to a significant increase of catchment erosion, as well as a consistent decline in inferred lake-water total organic carbon (TOC) levels and sediment carbonate accumulation. This process of recent deforestation may significantly reduce the role of lake systems to act as carbon sinks through hampering of both the soil organic carbon flux and the dissolution of catchment carbonate. The decline in lake-water TOC in Lugu Lake further increased algal production (i.e. tracked through sediment trends in chlorophyll a and its main diagenetic products) and changes in diatom composition. In comparison, there was little variation of sediment carbonate content in Chenghai Lake, which has a long history of catchment deforestation, while both primary production and lake-water TOC increased following cultural eutrophication during the last three decades. Furthermore, regional warming was associated with an increase in small-sized diatoms in both deep lakes, likely due to enhanced thermal stability. This study highlights the significant role of vegetation cover and land use in driving aquatic carbon cycling and phototrophs, revealing that deforestation can strongly reduce both inorganic and organic carbon export to lakes and thus aquatic carbon storage in karst landscapes.

Variability of TOC and DBPs (THMs and HAA5) in drinking water sources and distribution system in drought season: the North Iran case study.

The aim of this study is tracing seasonal variability of total organic carbon (TOC), trihalomethanes (THMs) and haloacetic acids (HAA5) as disinfection by-products (DBPs) in drinking water sources and the distribution system in the north of Iran. The results showed that the concentrations of TOC were within the range of 0.013-1.42 mg/L. In addition, the results showed that most of the water sources had nearly the same concentration level (i.e. <1 mg/L), with the exception of one peak for groundwater source and middle drinking water distribution system in the city of Sari (1.42 mg/L) and Babol (1.37 mg/L). It was demonstrated that brominated HAA (MBAA) presented the highest concentration in the Sari City (17.3 µg/L) followed by the City of Behshahr (8.9-11.19 µg/L). The Babol City showed the highest concentration of chlorinated HAA (22.403 and 22.503 µg/L for DCAA and TCAA, respectively). Among the different compounds of THMs, the concentration of CHBr3 was nearly in the same order of magnitude in the cities of Sari, Babol and Behshahr for both spring and summer seasons. The brominated THM (BDCM) concentrations were also high (14.7 µg/L) in the Behshahr City. The results of independent t-test indicated that the seasonal (spring and summer) difference was statistically significant in the case of temperature and TTHM (p < 0.05). Furthermore, total HAA5 ≤ 60 µg/L and THM ≤100 µg/L in all the considered cities over the period of the study. The TTHMs concentration was 56 µg/L in treating surface water (TSW) source in the summer season at the Sari city.

Distribution of natural and anthropogenic radionuclides in sediments from the Vefsnfjord, Norway.

Areas in central Norway were heavily contaminated with fallout from the Chernobyl accident in 1986. In this study, we assess 137Cs in surface sediments and sediment cores collected in the Vefsnfjord in Nordland county. Concentrations of 137Cs in surface sediments ranged from 159 to 191 Bq kg-1 dry weight (d.w.). Sub-surface peaks of 137Cs were observed in all cores, with a maximum concentration of 432 Bq kg-1 d.w. Given that little is known about the distribution of naturally occurring radionuclides in Norwegian fjords and coastal areas, a better understanding of the total burden of radioactivity is important for the Norwegian fishing and aquaculture industries. Therefore, analyses of the natural radionuclides 40K, 226Ra, 228Ra and 210Pb were included in the study. Analyses of total sulphur (TS), total carbon (TC), total organic carbon (TOC) and grain size distribution have been performed to provide a sedimentologic context for interpreting the radionuclide results.

Dual radicals-enhanced wet chemical oxidation of non-biodegradable chemicals.

Total organic carbon (TOC) has been suggested and utilized as an index of organic matter in aqueous phases. The overall performance of TOC is highly dependent on the method of oxidation of organic matter to carbon dioxide, such as high-temperature combustion (HTC) and wet chemical oxidation (WCO). HTC requires more energy and maintenance cost, it is a major barrier to the field application. In contrast, WCO is more suitable for the application of on-line monitoring systems due to requiring lower energy and easy maintenance. However, WCO shows lower oxidation than HTC, thus, oxidation performance should be improved for the application to the field. In this study, a dual radical system (DRS), including sulfate and hydroxyl radicals, was proposed to enhance oxidation ability. The DRS uses alkaline pH and persulfate to generate sulfate radicals, which have been used to activate hydroxyl radicals and oxidize organic matter. The oxidation mechanism for the DRS has been verified using model chemicals with different reaction rate constants. The applicability of the DRS has been confirmed using authentic wastewater with a high concentration of chloride. In this study, the DRS showed similar performance compared to the HTC within 10 % error range. The DRS shows similar oxidation performance with HTC even at a high concentration of chloride. DRS did not show interference by the presence of chloride up to 30,000 mg/L of chloride. Results of this study indicate that the DRS can enhance overall oxidation performance compared to the conventional WCO system.

A novel electrocoagulation electrode configuration for the removal of total organic carbon from primary treated municipal wastewater.

In this paper, the removal of total organic carbon (TOC) from a primary treated municipal wastewater using a new electrode configuration in electrocoagulation was evaluated. The used electrode configuration induces a dielectrophoretic (DEP) force by using an asymmetrical aluminum electrode with an alternating current power supply. The impact of applied current, electrolysis time, and interelectrode distance on the removal efficiency of TOC were evaluated. The experimental results showed that the maximum removal efficiency of TOC was obtained at 30 min electrolysis time, 600 mA applied current, and 0.5 cm interelectrode distance. Under these operating conditions, the TOC removal was 87.7% compared to 80.5% using symmetrical aluminum electrodes with no DEP effect. The energy consumption at the selected operating conditions was 3.92 kWh/m3. The experimental results were comparable with the simulation results done by COMSOL Multiphysics software.

Use of biochar to produce reclaimed water for irrigation use.

Emerging contaminants, especially, pharmaceutical and personal care products (PPCPs) are not removed well during conventional wastewater treatment and hence pose water quality risk to the environment and potentially to public health. Long-term use of reclaimed wastewater for irrigation can lead to accumulation of trace contaminants in the soil, ground water and their subsequent uptake by plants and potentially can enter human food chain. This paper uses biochar as an adsorbent to remove emerging contaminants from treated wastewater by performing fixed bed experiments. Ten emerging contaminants namely, carbamazepine (CBZ), caffeine, diethyltoluamide (DEET), diphenhydramine (DPH), meprobamate (MPB), primidone (PMD), sulfamethoxazole (SMX), fluoxetine (FXT), perfluorooctanoic acid (PFOA) and trimethoprim (TMP) were monitored during lab scale experiments. Results from the continuous flow runs showed that the breakthrough curve for compounds caffeine, CBZ, DEET and PFOA follow second order Thomas model with adsorption capacities of 396 µg g-1, 392 µg g-1, 1160 µg g-1 and 32 µg g-1 biochar, respectively. Whereas compounds such as DPH, TMP and FXT were completely removed throughout the column runs by biochar. Results for rest of the compounds were interfered by leaching of these compounds from biochar. It was observed that commercially available GAC performed much better than biochar for all the compounds considered. Even at 1% of obtained capacity, biochar amendment to soils where reclaimed water is used for irrigation can reduce the uptake of these compounds by plants.

[Spatial Distribution and Pollution Evaluation of Carbon, Nitrogen, and Phosphorus in Sediments of Zhushan Bay at Taihu Lake].

To reveal the distribution characteristics of carbon, nitrogen and phosphorus in the sediments of Zhushan Bay at Taihu Lake, sedimentary columns were collected and sliced by 2 cm vertically from ten sampling points in three sections of Zhushan Bay. The content of total nitrogen (TN), total phosphorus (TP), and total organic carbon (TOC) were determined for each slice to reveal their horizontal and vertical distribution. The results showed that:spatially, the content of TN, TP, and TOC increased in the surface sediments of Zhushan Bay from the open lake area to the bay, and inside the bay these indexes were significantly higher than in the open lake area (P<0.01). The content of TN, TP, and TOC in the surface sediments in the bay (section A) were 1.53 mg·g-1, 1.55 mg·g-1, and 11.31 mg·g-1, respectively, while in the surface sediments near the open lake (section C) they were only 0.75 mg·g-1, 0.57 mg·g-1, and 6.70 mg·g-1, respectively. Vertically, a feature of surficial enrichment was shown, and the contents of carbon, nitrogen and phosphorus in all three sections showed a decreasing trend with increase of depth. The contents of TN, TP and TOC in the surface sediments are 2-3 times, 2-5 times, and 2-3 times those in the bottom sediments, respectively. Generally, the average TP content in the sediment of Zhushan Bay is 0.93 mg·g-1, suggesting an apparent heavy pollution, while the average TN content is 1.11 mg·g-1 as slight pollution. According to the organic nitrogen index and comprehensive pollution index, the northern part of Zhushan Bay is suffering from heavy pollution, where the organic pollution is relatively strong. The TP pollution index is between 1.03 and 3.87, indicating heavy pollution in Zhushan Bay.

Evaluation of urea removal by persulfate with UV irradiation in an ultrapure water production system.

The removal of urea by persulfate with UV irradiation in an ultrapure water (UPW) production system was examined using a continuously operated column reactor. Urea is a substance that is not properly removed by the unit processes in UPW production systems. Based on our monitoring of urea concentration over 1 year of the operation of a UPW production facility, a relatively high concentration of urea was introduced between February and May in 2016 and the total organic carbon (TOC) concentration of the UPW was increased in that period. Approximately 50% of the urea in the raw water was removed by the UPW production process, for which double-pass reverse osmosis units were instrumental. The addition of persulfate to the TOC reduction UV unit in the UPW production process was examined to improve the efficiency of urea removal. As a result, supplying over 20 µmol/L persulfate to the TOC reduction UV reactor improved the efficiency of urea removal from 9% to 90%. UV dose was an important factor of urea removal. In the ion analysis, nitrate and sulfate were detected in the effluent, and the ratio of produced nitrate to the removed urea was approximately 2.

Effects of the presence of nanoscale zero-valent iron on the degradation of polychlorinated biphenyls and total organic carbon by sediment microbial fuel cell.

The degradation of polychlorinated biphenyls (PCBs) and total organic carbon (TOC) by sediment microbial fuel cell (SMFC) with/without nanoscale zero-valent iron (NZVI) addition was investigated. It was found that the combined application led to the highest removal efficiencies of PCBs (37.55 ±â€¯1.11%) and TOC (49.72 ±â€¯1.54%) in all circumstances and produced a higher power density (108.89 mW/m2) and a corresponding lower internal resistance (264 Ω) than operation employing SMFC only. The TOC removal efficiency and the total production of electricity were linear. High-throughput sequencing of anodic microbial communities indicated that the electrode participation can increase the abundance of electrogenic bacteria (Geobacter and Pseudomonas) and the NZVI addition can reduce the oxidation reduction potential of the system and therefore enrich some bacteria (Longilinea and Desulfofustis) beneficial to the degradation of organic matter.

Investigating the photo-Fenton process for treating soil washing wastewater.

PURPOSE: Petroleum hydrocarbons have created numerous problems for water resources. The main objective of this study was focused on the application of advanced oxidation processes (AOPs) in treatment of effluent of petroleum contaminated soil washing operation. METHODS: The AOP process in the present study was run with Fe2+/H2O2 (Fenton's reagent), Fe2+/H2O2/UV (photo-Fenton's reagent) and UV lamp (medium pressure mercury lamp, 400 W) in the batch-mode reactor at laboratory-scale. RESULTS: Various parameters and optimized values which could maximize the removal efficiency of COD were: Fe2+ = 0.1 g/L, H2O2 = 1 g/L, pH = 3 and irradiation time of 120 min. Under the optimal conditions, the removal efficiency of COD and TOC were achieved 86.3% and 68% respectively. The results showed that the reaction of the oxidation of diesel fuel by Fenton and photo-Fenton systems followed second-order kinetic model with reaction rate constants (k) of 7 × 10-6 and 3 × 10-6 l/mg min-1 respectively. CONCLUSIONS: The photo-Fenton process can be used as an effective and environmental friendly method in the degradation of petroleum organic compounds.