Regeneration and Reuse of a Seaweed‐Based Biosorbent in Single and Multi‐Metal Systems

A seaweed‐waste material resulting from the processing of Ascophyllum nodosum was previously shown to be very efficient at removing Zn(II), Ni(II) and Al(III) both in single and multi‐metal waste streams. In this study, the regeneration of the biosorbent using an acid wash resulted in the release of high metal concentrations during multiple desorption cycles. Maximum desorption efficiencies (DE) of 183, 122 and 91% were achieved for Zn(II), Ni(II) and Al(III), respectively, for subsequent metal loading cycles, significantly exceeding the desorption rates observed for conventional sorbents. The regeneration of the sorbent was accomplished with very little loss in metal removal efficiency (RE) for both single and multi‐metal systems. Values of 92, 96 and 94% RE were achieved for Zn(II), Ni(II) and Al(III), respectively, for the 5^th sorption cycle in single metal aqueous solutions. A slight decrease was observed for the same metals in multi‐metal systems with maximum REs of 85, 82 and 82% for Zn(II), Ni(II) and Al(III), respectively. This study showed that the novel sorbent derived from a seaweed industrial waste would be suitable for multiple metal sorption cycles without any significant loss in RE.     

Assessment of Urban Source Metal Levels in Influent,Effluent, and Sludge of Two Municipal Biological Nutrient Removal Wastewater Treatment Plants of Bursa,an Industrial City in Turkey

Removal of Al, As, Cd, total Cr (Tot. Cr), Cu, Total Fe (Tot. Fe), Mn, Ni, Pb, Sb, Sn, and Zn from urban effluent by wastewater treatment plants (WWTPs) operated under five‐stage Bardenpho® process were investigated and water soluble metals in the dewatered sludge were quantified. Samples were collected from two WWTPs on a weekly basis over an approximately 2.5‐year time span. Tot. Fe and Al were the most abundant, As, Pb, Ni, Cu, and Cd were the least abundant metals in the influents of both WWTPs. Removal efficiencies above 75% were achieved for Tot. Cr, Tot. Fe, Al, and Cu, whereas, no significant removal was observed for As, Cd, Pb, Sb, and Sn. Removal of Tot. Cr, Cu, Tot. Fe, Zn, Al, Mn, and Ni were influenced by influent suspended solids concentrations, and of Tot. Cr, Zn, and Cd were influenced by their initial content in the influent. Zn removal efficiency of biological nutrient removal (BNR) system in this study was higher and Cd removal efficiency was lower than that of conventional activated sludge reported in the literature. No remarkable difference for metals such as Cu, Mn, Ni, and Pb was observed between the removal efficiencies of conventional system and BNR system.     

Biosorption of Cd(II), Ni(II) and Pb(II) from Aqueous Solution by Dried Biomass of Aspergillus niger: Application of Response Surface Methodology to the Optimization of Process Parameters

In this study, the biosorption of Cd(II), Ni(II) and Pb(II) on Aspergillus niger in a batch system was investigated, and optimal condition determined by means of central composite design (CCD) under response surface methodology (RSM). Biomass inactivated by heat and pretreated by alkali solution was used in the determination of optimal conditions. The effect of initial solution pH, biomass dose and initial ion concentration on the removal efficiency of metal ions by A. niger was optimized using a design of experiment (DOE) method. Experimental results indicated that the optimal conditions for biosorption were 5.22 g/L, 89.93 mg/L and 6.01 for biomass dose, initial ion concentration and solution pH, respectively. Enhancement of metal biosorption capacity of the dried biomass by pretreatment with sodium hydroxide was observed. Maximal removal efficiencies for Cd(II), Ni(III) and Pb(II) ions of 98, 80 and 99% were achieved, respectively. The biosorption capacity of A. niger biomass obtained for Cd(II), Ni(II) and Pb(II) ions was 2.2, 1.6 and 4.7 mg/g, respectively. According to these observations the fungal biomass of A. niger is a suitable biosorbent for the removal of heavy metals from aqueous solutions. Multiple response optimization was applied to the experimental data to discover the optimal conditions for a set of responses, simultaneously, by using a desirability function.     

Biosorption of Cd(II) and Zn(II) by Nostoc commune: Isotherm and Kinetics Studies

In this study, Nostoc commune (cyanobacterium) was used as an inexpensive and efficient biosorbent for Cd(II) and Zn(II) removal from aqueous solutions. The effect of various physicochemical factors on Cd(II) and Zn(II) biosorption such as pH 2.0–7.0, initial metal concentration 0.0–300 mg/L and contact time 0–120 min were studied. Optimum pH for removal of Cd(II) and Zn(II) was 6.0, while the contact time was 30 min at room temperature. The nature of biosorbent and metal ion interaction was evaluated by infrared (IR) technique. IR analysis of bacterial biomass revealed the presence of amino, carboxyl, hydroxyl, and carbonyl groups, which are responsible for biosorption of Cd(II) and Zn (II). The maximum biosorption capacities for Cd(II) and Zn(II) biosorption by N. commune calculated from Langmuir biosorption isotherm were 126.32 and 115.41 mg/g, respectively. The biosorption isotherm for two biosorbents fitted well with Freundlich isotherm than Langmuir model with correlation coefficient (r² < 0.99). The biosorption kinetic data were fitted well with the pseudo‐second‐order kinetic model. Thus, this study indicated that the N. commune is an efficient biosorbent for the removal of Cd(II) and Zn(II) from aqueous solutions.     

Preparation,Characterization of a Novel Chelating Resin Functionalized with o‐Hydroxybenzamide and Its Application for Preconcentration of Trace Metal Ions

A stable extractor of metal ions was synthesized through azo linking of o‐hydroxybenzamide (HBAM) with Amberlite XAD‐4 (AXAD‐4) and was characterized by elemental analyses, IR spectral, and thermal studies. Its water regain value and hydrogen ion capacity were found to be 12.93 and 7.68 mmol g^?1, respectively. The optimum pH range (with the half‐loading time [min], t_1/2) for Cu(II), Cr(III), Ni(II), Co(II), Zn(II), and Pb(II) ions were 2.0–4.0 (5.5), 2.0–4.0 (7.0), 2.0–4.0 (8.0), 4.0–6.0 (9.0), 4.0–6.0 (12.0), and 2.0–4.0 (15.0), respectively. Comparison of breakthrough and overall capacities of the metals ascertains the high degree of column utilization (>70%). The overall sorption capacities for Cu(II), Cr(III), Ni(II), Co(II), Zn(II), and Pb(II) ions were found to be 0.29, 0.22, 0.20, 0.16, 0.13, and 0.11 mmol g^?1 with the corresponding preconcentration factor of 400, 380, 380, 360, 320, and 320, respectively. The limit of preconcentration was in the range of 5.0–6.3 ng mL^?1. The detection limit for Cu(II), Cr(III), Ni(II), Co(II), Zn(II), and Pb(II) were found to be 0.39, 0.49, 0.42, 0.59, 0.71, and 1.10 ng mL^?1, respectively. The AXAD‐4‐HBAM has been successfully applied for the analysis of natural water, multivitamin formulation, infant milk substitute, hydrogenated oil, urine, and fish.     

Sorption von Schwermetallen durch Eisenphosphat-Kolloide in essigsauren Bodenextrakten

Sorption of Heavy Metals from Acetic Acid Extracts by Ferric Phosphate Colloids A conceivable procedure to remedy heavy metal contaminated soil materials is given with extraction of organic acids, i. e. by the use of a biological degradable extraction agent. The following concentration step of heavy metal extracts should be carried out to a great extent without a change of the low pH values. A conventional precipitation of the heavy metals by rising the pH should be avoided in order to introduce no large amounts of salts into the wastewaters of the process and furthermore, to reduce the amount of sludge to be deposited. The process scheme developed with the objective of heavy metals recycling consists of the following steps: the extraction of the heavy metal contaminated soils with weak organic acids like acetic acid or citric acid, the electrolysis of the extract, and a concentration step in order to treat metal concentrations not fully removed by electrolysis. This third step, e.g. could contain sorption on iron phosphate colloids and precipitation within the acidic environment. It has been examined whether a removal of the heavy metals Pb, Cd, Cu, Sb, Cr, Ni and Zn from acetic aqueous solutions of pH between 2 and 3 can be carried out.     

Phytoremediation of Sb,As, Cu,and Zn from Contaminated Water by the Aquatic Macrophyte Eleocharis acicularis

Sb, As, Cu, and Zn toxicity and contamination have become a growing concern in recent years. Phytoremediation, a plant based and cost effective technology, may be an effective approach in the cleanup of water contaminated by these metals. In this study, the aquatic macrophyte Eleocharis acicularis was used in laboratory and field experiments to assess its capability to accumulate Sb, As, Cu, and Zn, and thereby investigate its potential application in phytoremediation. The results showed that E. acicularis adapted well to water contaminated by these metals. The removal rates of Sb, As, Cu, and Zn in the laboratory experiment were 3.04, 2.75, 0.417, and 1.49 μg/L/day, respectively. The highest concentrations of these metals accumulated in E. acicularis after 10 days of the laboratory experiment were 6.29, 6.44, 20.5, and 73.5 mg/kg dry weight, respectively. Only 8% of As, 12% of Sb, 87% of Cu and 93% of Zn removed from the water were used by E. acicularis. The highest concentrations of Sb, As, Cu, and Zn accumulated in E. acicularis after 10 wk of the field experiment were 76.0, 22.4, 33.9, and 266 mg/kg dry weight, respectively. The results indicate that E. acicularis has the ability to accumulate Sb, As, Cu, and Zn from contaminated water.     

Assessment of Metal Pollution in Water and Surface Sediments of the Seyhan River,Turkey, Using Different Indexes

The aim of this study was to assess the level of heavy metals (Al, Cd, Cr, Cu, Fe, Mn, Ni, Pb, and Zn) contamination and enrichment in the surface sediments of the Seyhan River, which is the receiving water body of both treated and untreated municipal and industrial effluents as well as agricultural drainage waters generated within Adana, Turkey. Sediment and water samples were taken from six previously determined stations covering the downstream of the Seyhan dam during both wet and dry seasons and the samples were then analyzed for the heavy metals of concern. When both dry and wet seasons were considered, metal concentrations varied significantly within a broad range with Al, 7210–33 967 mg kg^?1 dw; Cr, 46–122 mg kg^?1 dw; Cu, 6–57 mg kg^?1 dw; Fe, 10 294–26 556 mg kg^?1 dw; Mn, 144–638 mg kg^?1 dw; Ni, 82–215 mg kg^?1 dw; Pb, 11–75 mg kg^?1 dw; Zn, 34–146 mg kg^?1 dw in the sediments while Cd was at non‐detectable levels for all stations. For both seasons combined, the enrichment factor (EF) and the geo‐accumulation index (I_geo) for the sediments in terms of the specified metals ranged from 0.56 to 10.36 and ?2.92 to 1.56, respectively, throughout the lower Seyhan River. The sediment quality guidelines (SQG) of US‐EPA suggested the sediments of the Seyhan River demonstrated “unpolluted to moderate pollution” of Cu, Pb, and Zn, “moderate to very strong pollution” of Cr and Ni. The water quality data, on the other hand, indicated very low levels of these metals suggesting that the metal content in the surface sediments were most probably originating from fine sediments transported along the river route instead of water/wastewater discharges with high metal content.     

Selective Separation and Preconcentration of Fe(III) and Zn(II) Ions by Solvent Extraction Using a New Triketone Reagent

A simple, rapid, and accurate method was developed for separation and preconcentration of trace levels of iron(III) and zinc(II) ions in environmental samples. Methyl‐2‐(4‐methoxy‐benzoyl)‐3‐(4‐methoxyphenyl)‐3‐oxopropanoylcarbamate (MMPC) has been proposed as a new complexing agent for Fe(III) and Zn(II) ions using solvent extraction prior to their determination by flame atomic absorption spectrometry (FAAS). Fe(III) and Zn(II) ions can be selectively separated from Fe(II), Pb(II), Co(II), Cu(II), Mn(II), Cr(III), Ni(II), Cd(II), Ag(I), Au(III), Pd(II), Cr(VI), and Al(III) ions in the solution by using the MMPC reagent. The analytical parameters such as pH, sample volume, shaking time, amount of MMPC reagent, volume of methyl isobutyl ketone (MIBK), effect of ionic strength, and type of back extractant were investigated. The recovery values for Fe(III) and Zn(II) ions were greater than 95% and the detection limits for Fe(III) and Zn(II) ions were 0.26 and 0.32 µg L^?1, respectively. The precision of the method as the relative standard deviation changed between 1.8 and 2.1%. Calibration curves have a determination coefficient (r²) of at least 0.997 or higher. The preconcentration factor was found to be 100. Accuracy of the method was checked by analyzing of a certified reference material and spiked samples. The developed method was applied to several matrices such as water, hair, and food samples.     

Seasonal distribution of trace metals in suspended particulate and bottom sediments of four microtidal river estuaries,west coast of India

ABSTRACT

The seasonal distribution of metals (V, Cr, Co, Cu, Ni, Zn, Pb, Mn, Fe, Al and Ti) in suspended and bottom sediments of four minor estuaries (Terekhol, Chapora, Sal and Talpona rivers) of Goa, India was investigated to understand the metal distribution process in the estuarine region. The highest particulate-metal concentrations were found in low-salinity regions of all the estuaries, in the wet season (e.g. in the Terekhol River, the averages in ppm were Co: 53, Ni: 197, Cu: 208, Zn: 212 and Pb: 65) compared to the dry season averages (Co: 27, Ni: 76, Cu: 105, Zn: 164 and Pb: 13 ppm). The estuarine-mixing diagrams showed non-conservative behaviour in both seasons. The Sal River had the highest particulate-metal concentration (Co: 106, Ni: 300 and Zn: 323 ppm), suggesting an anthropogenic input. The enrichment factor for suspended matter was higher than bottom sediments with extremely high enrichment for Mn (>10). The Geo-accumulation index displayed unpolluted to polluted class for all metals. The study highlights the important role played by small estuaries in seasonal metal release and accumulation along the coastal region.     

Adsorption of Chromium(III), Nickel(II), and Copper(II) from Aqueous Solution by Activated Alumina

The possible use of activated alumina powder (AAP) as adsorbent for Cr(III), Ni(II), and Cu(II) from synthetic solutions was investigated. The effect of various parameters on batch adsorption process such as pH, contact time, adsorbent dosage, particle size, temperature, and initial metal ions concentration were studied to optimize the conditions for maximum metal ion removal. Both higher (molar) and lower (ppm) initial metal ion concentration sets were subjected to adsorption on AAP. Adsorption process revealed that equilibrium was established in 50 min for Cr(III) at pH 4.70, 80 min for Ni(II) at pH 7.00, and 40 min for Cu(II) at pH 3.02. Percentage removal was found to be highest at 55°C for Cr(III) and Ni(II) with 420 µm and 45°C for Cu(II) with 250‐µm particle size AAP. A dosage of 2 g for Cr(III), 8 g for Ni(II), and 10 g Cu(II) gave promising data in the metal ion removal. The adsorption process followed Langmuir as well as Freundlich models. The thermodynamics of adsorption of these metal ions on activated aluminum indicated that the adsorption was spontaneous and endothermic in nature. Present study indicates that AAP can act as a promising adsorbent for industrial wastewater treatment.     

Kinetics,Mechanistic and Thermodynamics of Zn(II) Ion Sorption: A Modeling Approach

Biosorption potential of Cedrus deodara sawdust (CDS) in terms of sorption of Zn(II) ion across liquid phase has been evaluated in the present investigation. The surface of the CDS biomass before the sorption of Zn(II) ions seemed to be more porous, non‐crystalline and heterogeneous. The maximum uptake capacity of CDS was 97.39 mg g^?1. Sorption of Zn(II) ion on the surface of CDS sawdust was maximum at pH 5, temperature 45°C, initial concentration of Zn(II) ion 100 mg L^?1, biomass dose 1 g L^?1, contact time 150 min, and agitation rate 160 rpm. Pseudo second‐order kinetics with the highest linear regression coefficient (R² = 0.99), and lowest values of error functions, i.e., chi (χ²) and sum of square errors (SSE) against pseudo first‐order rate kinetics showed that the sorption of Zn(II) ion on the surface of CDS was mediated by chemosoprtive forces of attraction rather than physical adsorption. Mechanistically, relatively higher proportion of sorption of Zn(II) ion in early phase of contact time was profoundly explained by Bangham's equation and film diffusivity (D^f). Intraparticle or pore diffusion (D_p) of Zn(II) ion inside the pores of CDS was rate limiting step at the later stage of contact time. Furthermore, the thermodynamic study on sorption of metal ion delineated the fact that the Zn(II) sorption on the surface of CDS was spontaneous, endothermic together with increased entropy at solid liquid interface.     

太湖流域滆湖底泥重金属赋存特征及其生物有效性

为了探讨太湖流域滆湖底泥重金属(Cd、Cr、Cu、Zn、Ni和Pb)的赋存特征及其生物有效性,对底泥重金属总量、形态以及生物富集量进行了分析.结果表明,6种重金属含量的空间分布表现为北部湖区最高,其次为南部湖区,中部湖区最低,重金属Ni、Cu、Zn和Pb含量显著高于沉积物背景值,分别是背景值的4.77、3.89、2.96和2.76倍,重金属总量与沉积物中的黏土成分含量具有显著相关性.采用三级四部提取法对重金属形态进行分析表明,6种重金属的生物有效态(弱酸结合态、可还原态和可氧化态之和)含量顺序为CdCuZnPbNiCr,其中Cd、Cu、Zn和Pb的生物有效态含量分别占总量的84.15%、78.47%、76.50%和64.29%.Cu和Zn在铜锈环棱螺中富集含量要显著高于其他金属元素.相关性分析表明,6种重金属中仅Cr和Pb的生物富集量与有效态含量具有显著相关性,这表明,重金属在生物体内的富集不仅与有效态含量有关,还与底泥重金属总量有关.因此,评价滆湖重金属的生态风险时需要综合考虑重金属的总量及生物有效态含量.     

Removal of As,Cd, Cu,Ni, Pb,and Zn from a highly contaminated industrial soil using surfactant enhanced soil washing

Surfactant enhanced soil washing (SESW) was applied to an industrial contaminated soil. A preliminary characterization of the soil regarding the alkaline-earth metals, Na, K, Ca and Mg took values of 2866, 2036, 2783 and 4149 mg/kg. The heavy metals As, Cd, Cu, Pb, Ni and Zn, had values of 4019, 14, 35582, 70, 2603, and 261 mg/kg, respectively. When using different surfactants, high removal of Cu, Ni and Zn were found, and medium removals for Pb, As and Cd. In the case of these three metals, tap water removed more than the surfactant solutions, except for the case of As.There were surfactants with average removals (this is, the removal for all the metals studied) of 67.1% (Tween 80), 64.9% (Surfacpol 14104) and 61.2% (Emulgin W600). There were exceptional removals using Texapon N-40 (83.2%, 82.8% and 86.6% for Cu, Ni and Zn), Tween 80 (85.9, 85.4 and 81.5 for Cd, Zn and Cu), Polafix CAPB (79%, 83.2% and 49.7% for Ni, Zn and As). The worst results were obtained with POLAFIX LO with a global removal of 45%, well below of the average removal with tap water (50.2%).All removal efficiencies are reported for a one step washing using 0.5% surfactant solutions, except for the case of mezquite gum, where a 0.1% solution was employed.     

云南属都湖沉积物金属元素地球化学

通过对属都湖短岩芯Esdrl重金属元素的分析,结合沉积物粒度、流域降水和人类活动资料,讨论属都湖沉积物金属元素地球化学变化特征.结果表明.沉积物中AI、Mg、Co、Zn、Cr、Ti、V、Cu、Ni等元素含量变化与粘土含量、夏季降水量显著相关,降水导致的流域侵蚀强弱变化是影响元素含量变化的主要因素.元素Pb含量从岩芯底部到顶部总体呈上升趋势,25-17.5cm沉积物中Pb含量较稳定主要为自然侵蚀过程控制;17.5-10.5cm沉积物中Pb含量迅速增加后逐渐降低推测为20世纪50年代湖区附近矿山开采产生的粉尘沉降的影响;10.5-Ocm Pb含量逐渐增加,80年代以后大气中Pb含量上升.Pb在漉域的干湿沉降应是岩芯上部Pb含量升高的原因.在氧化还原作用下沉积物中Fe、Mn易在沉积物一水界面发生再迁移.25-7.5cm沉积物中的Fe、Mn含量变化特征为沉积后再迁移作用的结果;7.5-0cm Fe和bin含量明显上升,夏季降水量增加导致流域侵蚀增强和土壤的潜育化可能是岩芯上部Fe、Mn含量显著上升的原因.     

Adsorption of Metal Ions onto the Chemically Modified Agricultural Waste

This paper discusses about the adsorption of metal ions such as Cu(II), Cd(II), Zn(II), and Ni(II) from aqueous solution by sulfuric acid treated cashew nut shell (STCNS). The adsorption process depends on the solution pH, adsorbent dose, contact time, initial metal ions concentration, and temperature. The adsorption kinetics was relatively fast and equilibrium was reached at 30 min. The adsorption equilibrium follows Langmuir adsorption isotherm model. The maximum adsorption capacity values of the modified cashew nut shell (CNS) for metal ions were 406.6 mg/g for Cu(II), 436.7 mg/g for Cd(II), 455.7 mg/g for Zn(II), and 456.3 mg/g for Ni(II). The thermodynamic study shows the adsorption of metal ions onto the STCNS was spontaneous and exothermic in nature. The kinetics of metal ions adsorption onto the STCNS followed a pseudo‐second‐order kinetic model. The external mass transfer controlled metal ions removal at the earlier stages and intraparticle diffusion at the later stages of adsorption. A Boyd kinetic plot confirms that the external mass transfer was the slowest step involved in the adsorption of metal ions onto the STCNS. A single‐stage batch adsorber was designed using the Langmuir adsorption isotherm equation.     

云南阳宗海沉积物重金属污染时空特征及潜在生态风险

分析了阳宗海柱状及表层沉积物中Al、Fe、Mn、Zn、Cr、Co、Ni、Cu、As、Cd、Pb等金属元素的含量,结合沉积年代学,研究了沉积物重金属污染的时空变化和潜在生态风险特征.结果表明,表层沉积物中重金属含量具有一定的空间差异性,As、Cd、Cu、Pb和Zn在中东部湖区含量较高,而Cr、Co、Ni含量高值位于南、北湖区的近岸区域;柱状沉积物中,1990s之前As、Cd、Cu、Pb和Zn含量较为稳定,1990s中后期以来,其含量逐渐增加,并在2009-2010年前后达到最大值,此后逐渐下降;而柱状沉积物中Cr、Co、Ni含量变化趋势与Al、Fe相似,总体上由下向上逐渐降低,这主要与沉积物质地(粒度)逐渐变粗有关.重金属富集系数表明,阳宗海沉积物中主要污染元素为As、Cd、Cu、Pb和Zn,1990s中后期污染程度快速增加,2009-2010年前后达到峰值,此后污染程度逐渐降低;表层沉积物中Cu为未污染至"弱"污染水平;Zn、Pb为"弱-中等"污染水平,As为"中等-强"污染水平,Cd为"弱-强"污染水平,中东部湖区污染程度高于其他湖区,这可能与该湖区缺少入湖径流、自然碎屑物质沉积速率较低以及砷污染事件等人为源的重金属贡献影响更为显著有关.生态风险评价结果表明,在2002-2010年前后沉积物重金属达到"中等-强"潜在生态危害,主要贡献因子是Cd和As,近年来其生态风险等级逐渐降低;表层沉积物中重金属在中东部湖区具有"中等"程度潜在生态危害,而其他湖区表层沉积物重金属具有较低程度的潜在生态风险.     

Evaluation of metal contamination in coastal sediments of the Bay of Bengal, India: geochemical and statistical approaches

Surface sediment samples collected from the inner shelf region of the Bay of Bengal, were analysed for the major elements and total and acetic acid available trace elements (Al, Ca, Cd, Co, Cr, Cu, Fe, K, Mg, Mn, Na, Ni, P, Pb, Si, Zn) to evaluate geochemical processes influencing their distribution. Major elemental analysis showed that the sediments had high concentrations of Si and relatively low concentrations of Al and Fe. Both major elemental and trace metal concentrations indicated that the sediments represent weathered products of granite and charnockite. Normalization of metals to Al indicated relatively high enrichment factors for Pb, Cd, Zn and Cr. The higher proportions of nondetrital Pb (66%), Cd (41%) and Co (28%) reveal metal contamination due to anthropogenic inputs. Factor analysis (FA) identified six possible types of sedimentological and geochemical associations. The dominant factor accounting for 26.9% of the total variance identifies an anthropogenic input and accumulation of nondetrital Cd, Co, Cr, Ni and Pb. Association of these metals with CaCO3 reveals that shell fragments in the surface sediments are likely act as a carrier phase for nondetrital metals. The results are discussed in the context of the sources and pathways of elements in the Bay of Bengal.     

Distribution and ecological risk assessment of some heavy metals in coastal surface sediments along the Red Sea,Egypt

The ecological risk assessment for Al,Zn,Cu,Ni,V,Pb,Cd,and Hg in surface sediment collected from the Egyptian Red Sea coast was evaluated using the Geo-accumulation Index(I_(geo)).Sediment Enrichment Factor(SEF) and Potential Ecological Risk Index(PERI) methods.The predominant heavy metal,aluminum,showed high concentrations along both of Aqaba Gulf(4378.8 ± 2554.1 μg/g) and southern part of the Red Sea(2972.8 + 1527.5 μg/g).while it recorded the lowest concentration in Suez Gulf(829.7 ± 398.2 μg/g).The determined heavy metal concentrations had the order of Al Zn -Ni V Pb Cu Cd Hg.The statistical analyses showed some correlations among the heavy metals contents.Several international sediment quality guidelines were used to estimate the quality of the collected sediments.Interestingly,the recorded average heavy metals concentrations were lower than those of the permissible contents for sediment quality guidelines.The Geo-accumulation index calculations(I_(geo)) proved that the investigated region could be classified as an unpolluted area.Sediment Enrichment Factor(K_(SEF)) study showed high values in Suez Gulf region.The single pollution index analysis of heavy metals in the sediments(C~i_f) indicated that Al,Zn,V,and Pb were of natural origin,while Ni,Cd and Hg were seriously affected by human activities.Interestingly,amongst,all the determined heavy metals,Cd and Hg gave moderate ecological risk indicators.