Dye Removal,Energy Consumption and Operating Cost of Electrocoagulation of Textile Wastewater as a Clean Process

In this research, the efficiency of electrocoagulation treatment process using aluminum electrodes to treat synthetic wastewater containing Reactive Red198 (RR198) was studied. The effects of parameters such as voltage, time of reaction, electrode connection mode, initial dye concentration, electrolyte concentration, and inter electrode distance on dye removal efficiency were investigated. In addition, electrical energy consumption, electrode consumption, and operating cost at optimum condition have been investigated. The results showed that dye and chemical oxygen demand removals were 98.6 and 84%, respectively. Electrode consumption, energy consumption and operating cost were 0.052 kg/m³, 1.303 kWh/m³ and 0.256 US$/m³, respectively. Dye removal kinetic followed first order kinetics. It can be concluded that electrocoagulation process by aluminum electrode is very efficient and clean process for reactive dye removal from colored wastewater.     

Removal of the Alphazurine FG Dye from Simulated Solution by Electrocoagulation

The removal of Alphazurine FG (AF) dye from water by an electrocoagulation process has been studied. The effect of some operational parameters, such as anode material, current density, initial dye concentration, pH of solution, conductivity, and inter‐electrode distance, on the removal efficiency was investigated. Iron and aluminum were used as anodes in the electrocoagulation cell. It was found that the efficiency of the iron anode was better than that of the aluminum anode for AF removal. The factors that affected the removal efficiency were the current density and the initial dye concentration. The removal efficiency increased from about 35% at 25 A m^–2 to about 97% at 100 A m^–2, during 4 min of electrocoagulation. The results exhibited pseudo‐first‐order kinetics for AF removal by electrocoagulation. In addition, a mathematical model was successfully established for predicting the removal efficiency. A comparison between the model results and experimental data gave a high correlation coefficient (R² = 0.9925), which indicates that the model is able to predict the removal efficiency of AF.     

Electrocoagulation/Electroflotation Process for Removal of Organics and Microplastics in Laundry Wastewater

In the present research, laundry wastewater treatment is studied using the electrocoagulation/electroflotation process. For the optimization of treatment conditions such as electrode type (Al–Al, Al–Fe, Fe–Fe, and Fe–Al), initial pH (5–9), current (0.54–2.16 A), and application time (15–60 min), response surface methodology is used. Removal efficiencies of chemical oxygen demand (COD), color, anionic surfactant, microplastic, and phosphate are studied. It is determined that the most effective removal is obtained with 2.16 A current, pH 9, and 60 min reaction time using Fe–Al electrode. Here, 91%, 94%, 100%, and 98% removal efficiencies are achieved for COD, surfactant, color, and microplastic, respectively. The operating cost of the combined process is calculated as $1.32 m^?3 for the optimum removal parameters. The adsorption kinetics study shows that the removal follows second‐order kinetics. The laboratory‐scale test results indicate that the electrocoagulation/electroflotation process is feasible for the treatment of laundry wastewater.     

Fate and Behavior of Organochlorine Pesticides in the Indonesian Tropical Climate: A Study in the Segara Anakan Estuarine Ecosystem

The fate and behavior of organochlorine pesticides (OCPs) in the Segara Anakan Estuarine ecosystem was studied in the Indonesian tropical climate, which is characterized by heavy rainfall in the rainy season and low rainfall in the dry season. Since OCPs have high affinity for soil, a field study on the dissipation and degradation pattern of soil‐applied 1,1,1‐trichloro‐2,2‐bis (4‐chlorophenyl) ethane (p,p′‐DDT) and 1,1‐dichloro‐2,2‐bis (4‐chlorophenyl) ethylene (p,p′‐DDE) as model OCPs was carried out. They occurred at a faster rate in the biphasic mode in wet conditions and at a slower rate in dry conditions. In wet conditions, the conversion from p,p′‐DDT to p,p′‐DDE and p,p′‐DDD (1,1‐dichloro‐2,2‐bis (4‐chlorophenyl) ethane) was governed by a parallel reaction. In dry conditions, only p,p′‐DDE was formed. The fate and behavior of OCPs in sediment estuary are similar to those in soil under wet conditions, except that their sorption‐desorption constants are influenced by estuarine surface water salinity. In the dry season, due to high salinity, the sediment acts as an OCP sink and a secondary source for the ecosystem, causes higher OCP concentration of local bio‐monitors, i. e., Geloina spp. and Mugil spp. In the rainy season, high water inflow washed the desorbed OCP pesticides out of the estuarine ecosystem, and caused lower concentrations of bio‐monitors. A risk evaluation for the uptake of OCP pesticides during the dry season suggests that adult fish meal consumers are safe, but risk management is required for pregnant woman.     

Distribution of persistent organic pollutants in bivalves from the northeast coast of China

To assess the levels of organochlorine compounds (OCs) in the Chinese coastal environment, monitoring study using bivalves was conducted in 2005. A total of 21 bivalve samples covering the northeastern coast of China were collected and analyzed. Organochlorine compounds were widely distributed in the Chinese coastal environment, with dichlorodiphenyltrichloroethane (DDT) contamination being particularly prevalent. The overall concentrations of PCBs, DDTs, HCHs, chlordane compounds (CHLs), dieldrin, and endosulfans in bivalves were in the ranges of 3.27-25.4, 54.8-2680, 1.42-25.5, n.d. (not detected)-2.28, n.d.-4.02, and n.d.-9.55 ng g(-1) on a dry weight basis, respectively. The concentrations of DDT and HCH compounds are relatively higher than those from the coastal areas of other Asian countries. DDT metabolites were predominant, suggesting that the degradation of DDT is in progress in the Chinese coastal environment. Still, however, DDTs of high concentration exceeding 1000 ng g(-1) were observed at 19% of the stations surveyed. Among HCH compounds, beta-HCH, which is an isomer with strong persistency, was observed predominantly. Compositions of DDT and HCH compounds imply that fresh input of the two compounds into the Chinese coasts is possibly low.     

Polychlorinated biphenyls and organochlorine pesticides in plastics ingested by seabirds

The occurrence of plastic objects in the digestive tract was assessed in eight species of Procellariiformes collected in southern Brazil and the occurrence of polychlorinated biphenyls (PCBs) and organochlorine pesticides (OCPs) in the ingested plastics pellets and plastic fragments was evaluated. PCBs were detected in plastic pellets (491 ng g⁻¹) and plastic fragments (243-418 ng g⁻¹). Among the OCPs, p,p′-DDE had the highest concentrations, ranging from 68.0 to 99.0 ng g⁻¹. The occurrence of organic pollutants in post-consumer plastics supports the fact that plastics are an important source carrying persistent organic pollutants in the marine environment. Although transfer through the food chain may be the main source of exposure to POPs to seabirds, plastics could be an additional source for the organisms which ingest them, like Procellariiformes which are the seabirds most affected by plastic pollution.     

The occurrence of chemical elements and POPs in loggerhead turtles (Caretta caretta): an overview

Chemical elements and persistent organic pollutants (POPs) are globally present in aquatic systems and their potential transfer to loggerhead marine turtles (Caretta caretta) has become a serious threat for their health status. The environmental fate of these xenobiotics may be traced by the analysis of turtles’ tissues and blood. Generally, loggerhead turtles exhibited a higher metal load than other turtle species, this could be explained by differences in diet habits being food the main source of exposure. Literature shows that muscle, liver and kidney are most considered for the quantification of chemical elements, while, organic compounds are typically investigated in liver and fat.This paper is an overview of the international studies carried out on the quantification of chemical elements, polychlorinated biphenyls (PCBs), organochlorines (OCs) and perfluorinated compounds (PFCs), in tissues, organs and fluids of C. caretta from the Mediterranean Sea, the Atlantic and the Pacific Oceans.     

A review of pollutants in the sea-surface microlayer (SML): a unique habitat for marine organisms

Boundary layers between different environmental compartments represent critical interfaces for biological, chemical and physical processes. The sea-surface microlayer (uppermost 1-1000 microm layer) forms the boundary layer interface between the atmosphere and ocean. Environmental processes are controlled by the SML, and it is known to play a key role in the global distribution of anthropogenic pollutants. Due to its unique chemical composition, the upper organic film of the SML represents both a sink and a source for a range of pollutants including chlorinated hydrocarbons, organotin compounds, petroleum hydrocarbons, polycyclic aromatic hydrocarbons (PAH) and heavy metals. These pollutants can be enriched in the SML by up to 500 times relative to concentrations occurring in the underlying bulk water column. The SML is also a unique ecosystem, serving as an important habitat for fish eggs and larvae. Concentration ranges and enrichment factors of pollutants in the SML in different areas of the world's oceans have been critically reviewed, together with available toxicity data for marine biota found within the SML. Overall, the SML is highly contaminated in many urban and industrialized areas of the world, resulting in severe ecotoxicological impacts. Such impacts may lead to drastic effects on the marine food web and to fishery recruitment in coastal waters. Studies of the toxicity of fish eggs and larvae exposed to the SML contaminants have shown that the SML in polluted areas leads to significantly higher rates of mortality and abnormality of fish embryos and larvae.     

Relationship between age of waste and natural electric potential generation in Sanitary Landfill

The geophysical methods are effective tools for determining changes in physical parameters of the geological environment, as soil or groundwater in the presence of contamination. This work consisted on analyzing the natural electric potential obtained over domestic solid waste ditches with controlled closure dates. The interpretation data suggest the generation of electric potential predominantly through the redox phenomenon, as opposed to the flow potential phenomenon. The statistical data analysis indicates a correlation between residence time of the waste and growing variations of voltage. In addition highlights that eight years are required to achieve the reported values for the area with absence of waste, time estimated for decomposition of most organic matter contained in the buried waste.     

持久性有机污染物在中国湖库水体中的污染现状及分布特征

持久性有机污染物(POPs)在环境中广泛且持久存在,多数具有致畸、致癌、致突变等危害中国是全球湖泊密度较大的国家之一,湖泊在供水、渔业、维护生态系统多样性等众多方面发挥了重要作用湖泊是POPs的重要归宿之一湖泊水体中的POPs可被水生生物吸收利用并传递,对生态系统及人体健康构成较大危害因此湖泊水体中POPs的分布水平对周围的生态系统及人体健康有非常重要的影响本文收集、分析了2003年至2019年2月公开发表的80篇文献中的中国湖泊水体POPs数据,包括多环芳烃(PAHs)、六六六类农药(HCHs)、滴滴涕类农药(DDX)、多氯联苯(PCBs)、多溴联苯醚(PBDEs)、多氯联苯醚类(PCDEs)、全氟化合物(PFCs)及邻苯二甲酸酯类(PAEs),发现:目前中国已有水体POPs研究数据的湖泊共有49个,涉及19个省、直辖市、自治区,研究区域主要在东部地区(n=32),云贵高原(n=14)和青藏新疆湖区(n=3)少有研究,其它地区鲜有研究; PAHs、HCHs和DDX是研究最多的三类POPs,在中国湖泊水体中平均浓度分别为360.0±433.8 ng/L(n=26)、12.8±23.5 ...     

An Assessment of the Spatial Distribution of Polychlorinated Biphenyl Contamination in Turkey

This study summarizes the relevant information regarding the spatial distribution of polychlorinated biphenyls (PCBs) in various environmental (e. g., soil, sediment, air, water) and biological (e. g., fish, mussel, adipose tissue, milk) media in Turkey. The information sources used for this purpose, in addition to the scientific literature, were; official import records, governmental reports on monitoring of organochlorines, and reports prepared by international organizations. PCBs were never produced in Turkey; however they were imported and used within equipment or otherwise. The number of studies conducted on the topic is increasing significantly throughout the years and especially in the last decade. Evidence of PCB pollution was compared with the available background monitoring results from the region and other parts of the world, as well as relevant legislative standards. Overall, the presence of a number of important local PCB contamination sources is indicated as a result of this assessment.     

Persistent Organic Pollutants (POPs) in Bottom Sediments of the Vistula River,Poland

The Vistula (Wisla) river, the biggest river in Poland, is 1038 km long and has a drainage area of 168 689 km². The river is strongly polluted by wastewaters. Big industrial plants are situated mainly in the upper part of the river, where it is slow‐flowing. This paper presents the results of the analysis of bottom sediment samples gathered from different locations along the Vistula river, from Kraków to Gdansk. The study was conducted in 2005. The following parameters were determined: chloroorganic pesticides, polychlorinated biphenyls (PCBs), chlorophenols, polycyclic aromatic hydrocarbons (PAHs), total organic carbon (TOC). The sum of chloroorganic pesticides was in the range of 2.0 to 77.5 ng/g d.w. (dry wet) with the highest values in the upper part of the river. p,p′‐DDT was found in the highest concentration. The sum of PCBs was in the range of 0.9 to 64.2 ng/g d.w. The sum of chlorophenols varied from 0.48 to 14.3 ng/g d.w. 2,4‐Dichlorophenol and pentachlorophenol occurred in the highest concentration. The sum of PAHs was in the range of 1552 to 7832 ng/g d.w. Phenantren was found in the highest concentration and antracen in the lowest. TOC values varied from 4.3 to 43.9 g/kg d.w. The concentrations of pesticides and PCBs were the highest in the upper part of the river and decreased along the course of the river, but the other determined compounds did not show this trend. However, the highest values occurred always in the upper part of the river.     

Occurrence of persistent organic pollutants in marine fish from the Natuna Island,South China Sea

Five marine fish species were collected from the Natuna Island, South China Sea to investigate the occurrence of polybrominated diphenyl ethers (PBDEs), polychlorinated biphenyls (PCBs), dichlorodiphenyltrichloroethane and its metabolites (DDTs). Concentrations of PBDEs, PCBs, and DDTs in marine fish ranged from 2.85 to 7.82, 14.3 to 48.1, and 7.99 to 40.3 ng/g lipid weight, respectively. Higher concentrations of PBDEs, PCBs, and DDTs were observed in Snakefish (Trachinocephalus myops), which might be attributed to their different feeding and living habits. PCBs were the predominant POPs in all marine fish, followed by DDTs and PBDEs. BDE 47 and PCB 153 were the predominant congener of PBDEs and PCBs, respectively. Compositional distribution of DDTs indicated the possible presence of fresh input sources around the Natuna Island. The ratios of o,p′-DDT/p,p′-DDT being less than 1 in fish samples suggested that DDT contributions from dicofol seemed considerably low. New input sources of DDT in South China Sea are worth further research.     

Solid‐Phase Removal of Dissolved Organic Species from Water and Identification by GC–MS

A method is described for the detection and identification of dissolved organic compounds (DOCs) in various water samples. Acid treated active silica gel sorbent (pH 3) was packed into a micro‐column and used as a solid‐phase extraction medium for adsorption of DOCs. Silica particles‐adsorbed‐organic species were then divided into equal portions followed by suspension into various organic solvents of different polarities such as methanol, acetone, ethyl acetate, and toluene. Suspended silica‐adsorbed‐organic species were shaken for 1 h at room temperature and the organic extracts were subjected to GC–MS analysis under temperature programming conditions for qualitative detection and identification of these species. Blank solvents and silica samples were also subjected to the same extraction procedures and GC–MS analysis for comparison. The mass spectrum of each eluted chromatographic peak was library searched or manually interpreted to identify the compound.     

Persistent organic pollutants carried by synthetic polymers in the ocean environment

Thermoplastic resin pellets are melted and formed into an enormous number of inexpensive consumer goods, many of which are discarded after a relatively short period of use, dropped haphazardly onto watersheds and then make their way to the ocean where some get ingested by marine life. In 2003 and 2004 pre-production thermoplastic resin pellets and post-consumer plastic fragments were collected and analyzed for contamination for persistent organic pollutants (POPs). Samples were taken from the North Pacific Gyre, and selected sites in California, Hawaii, and from Guadalupe Island, Mexico. The total concentration of PCBs ranged from 27 to 980 ng/g; DDTs from 22 to 7100 ng/g and PAHs from 39 to 1200 ng/g, and aliphatic hydrocarbons from 1.1 to 8600 microg/g. Analytical methods were developed to extract, concentrate and identify POPs that may have accumulated on plastic fragments and plastic pellets. The results of this study confirm that plastic debris is a trap for POPs.     

Organochlorine pesticides and PCB residues in sediments of Alexandria Harbour,Egypt

Persistent organochlorine compound concentrations were determined for 23 surface sediment samples collected from Alexandria Harbor, Egypt. Total PCB concentrations ranged from 0.9 to 1210 ng/g with four to seven Cl-substituted biphenyls being the most prevalent PCBs congeners. Different PCB congener distribution patterns were observed, probably reflecting different inputs and attenuation at various locations. Total DDT concentrations varied from <0.25 ng/g to 885 ng/g. The ratios of DDTs (2,4^′- and 4,4^′-DDT)/total DDTs (DDTs plus metabolites) in sediment samples from certain sites were 0.86 or higher, indicating little attenuation or recent input of DDT. Total chlordane (the sum of heptachlor and its epoxide, oxy-, γ- and -chlordane and cis+trans-nonachlor) ranged from <0.25 to 44 ng/g with the highest concentration found in the Arsenal Basin. The geographic distributions of PCBs, total DDTs and total chlordane were similar. Chlorinated benzenes (CBs), hexachlorocyclohexanes (HCHs), aldrin, dieldrin, endrin, chloropyrifos, endosulfan, mirex and pentachloroanisole were below detection limits or detected at low concentrations in most of the samples. Sites that were contaminated with high concentrations of organochlorine compounds were associated with dense population and low energy environment. The contamination levels of PCBs, total DDTs and total chlordane were in high range compared to other locations worldwide.     

持久性有机污染物在中国湖泊生物中分布与富集的研究进展

持久性有机污染物(POPs)在环境中分布广泛且持久存在并具有高生物富集性,通常具有致癌、致畸、致突变等危害.湖泊是POPs的主要环境归宿之一,湖泊中的POPs可被水生生物富集并通过食物网传递,对生态系统及人体健康构成极大的危害.中国是POPs生产及使用大国,也是世界上湖泊较多的国家之一.湖泊生物尤其是水产品是中国人饮食中的重要组成部分,因此POPs在中国湖泊生物体中的富集对当地的生态系统和人体健康存在很大的潜在危害.本文通过收集、分析1997年—2017年7月公开发表的中国湖泊生物体POPs数据,发现中国湖泊生物中POPs富集研究主要集中在东部平原湖区,青藏高原及云贵高原湖区有少量研究;不同POPs在不同湖区湖泊生物中富集的含量存在较大差异,DDTs和HCHs在各湖区生物中普遍检出且存在明显差异,东部平原湖区生物体内多氯联苯、多溴联苯醚含量高于其他湖区生物体内含量,其他POPs在湖泊生物体内的富集研究相对较少且主要集中在东部湖泊.中国湖泊生物中DDTs、HCHs、多环芳烃、多氯联苯、多溴联苯醚、多氯苯并二英和多氯苯并呋喃、全氟化合物、全氟辛酸、有机锡及六溴环十二烷脂肪归一化后的平均含量分别为454.56±653.40、153.57±435.99、2849.49±3092.52、118.40±20.28、18.40±20.28、17.43±19.43、147.17±192.93、1542.18±1347.64、11380.75±5316.75和2.19±1.92 ng/g.POPs在中国湖泊生物体内的含量水平与生物所处营养级、脂肪含量和年龄呈正相关,但并非完全一致,还受到生活习性、生物物种与结构、生存环境及生物量等多种因素的影响;生物不同组织对POPs的富集能力有较大差异,内脏器官对POPs的富集能力明显高于肌肉组织.