POPs and their ecological risk in sewage sludge of waste water treatment plants in Beijing, China

The concentrations of three classes of persistent organic compounds (POPs) in the sewage sludge from 12 Beijing wastewater treatment plants (WWTPs) were investigated and their ecological risks were assessed. The concentrations of 15 polycyclic aromatic hydrocarbons (PAHs), 27 polychlorinated biphenyl congeners (PCBs) and 15 organochlorine pesticides (OCPs) in sewage sludge were measured using gas chromatography–tandem mass spectrometry (GC–MS/MS) technique. Total PAHs concentrations ranged from 445.1 to 3,586.4 ng g^?1 dry weight (dw), and the sum of the phenanthrene (Phe), anthracene (Ant), naphthalene (Nap), fluoranthene and chrysene accounted for 69.3–97.0 % of the total PAHs. The most abundant compounds present were 2-ring and 3-ring Ant, Phe and Nap, indicating a possible petrogenic source. Total PCBs concentrations were ranged between 3.2 and 21.8 ng g^?1 dw. Total OCPs concentrations ranged from 38.0 to 143.3 ng g^?1 dw, and the sum of total DDT, HCB and HCHs accounted for 69.6–97.7 % of the total OCPs. The levels of PAHs, PCBs and OCPs in this study were comparable to or lower than those reported in relatively WWTPs from other regions. In addition, they were also shown to have various distribution patterns, possibly due to their different wastewater sources. The 12 WWTPs may be classified into 4 groups because of their different sources of waste water based on cluster analysis. The ecological risk assessment shows that the concentrations of Ant or Fla at two sites, p,p′-DDE and ∑DDT at 83 % of the 12 sites may cause adverse ecological effects.     

Selective Separation/Preconcentration of Silver Ion in Water by Multiwalled Carbon Nanotubes Microcolumn as a Sorbent

The present paper proposes the application of multiwalled carbon nanotubes (MWCNTs) as a solid adsorbent for selective separation/preconcentration of silver(I) in water samples prior to flame atomic absorption spectrometry. The procedure is based on the solid phase extraction of Ag(I)–2‐mercaptobenzothiazole chelate on MWCNTs. The elution step is carried out with 5 mL of 2 mol L^?1 HNO₃ in acetone solution at a flow rate of 1.0 mL min^?1. The influences of the various analytical parameters including pH of the solution, eluent type, sample volume, flow rates of eluent, matrix ions were investigated for optimization of the presented procedure. Tests of addition/recovery for analyte ion in real samples were performed with satisfactory results. Preconcentration factor and limit of detection for Ag(I) were 160 and 0.21 µg L^?1, respectively. The synthesized MWCNT exhibited excellent stability in eluent solution and its adsorption capacity was 5.4 mg of silver per gram of sorbent. The proposed method was successfully applied to trace silver determination in a variety of environmental water samples.     

Determination of Copper in Water Samples after Solid‐phase Extraction Using Dimethylglyoxime‐modified Silica

This work describes the modification of silica gel with dimethylglyoxime, in order to prepare an effective sorbent for the preconcentration and determination of copper. The sorption capacity of dimethylglyoxime‐modified silica‐gel (DMGMS) was 71.37 mg g^–1 and the optimum pH for the quantitative recovery of copper was found to be 5.0. The optimum flow rate, sorbent amount, and sample volume were 1 mL min^–1, 300 mg, and 50 mL, respectively. 10 mL of 0.1 mol L^–1 HCl was the most suitable eluent. The detection limit of copper was 6.0 ng mL^–1. The recommended method, for the determination of copper, is simple and reliable, without any notable matrix effect and can be successfully applied to environmental water samples. Copper recovery in the range from 99–100% was obtained from seawater and thermal spring water using this method. The method was applied to standard reference materials, NIST‐1515 (apple leaves) and NIST‐1643e (simulated fresh water), for the determination of copper and the results were in good agreement with certified values.     

Separation and Preconcentration of Cobalt Using a New Schiff Base Derivative on Amberlite XAD‐7

In this study, a new solid‐phase extraction procedure has been developed for preconcentration and determination of Co ions in different water samples by flame atomic absorption spectrometry (FAAS). Cobalt was preconcentrated as N,N′‐bis(pyridine‐2‐yl‐methyl)benzene‐1,4‐diamine (Co‐BPMBDA) from sample solutions using a column containing Amberlite XAD‐7 and was determined. In order to achieve the best performance for the method, effects of several parameters such as pH, concentrations of ligand, sample flow rate, eluent, and matrix ions on the method efficiency were investigated. Under optimum conditions, the preconcentration factor was found to be 200 for 1000 mL waters samples. Detection limit based on the 3S_b criterion was calculated as 0.24 µg/L for 100 mL of sample solution and relative standard deviation was found to be 1.8%. The method was applied to determine the trace amounts of cobalt in water samples.     

Levels of Organohalogenated Pollutants in Human Milk Samples from Konya City,Turkey

This study reports the levels of organochlorine pesticides (OCPs, α‐, β‐, γ‐ and Δ‐HCHs, p,p′‐DDE, p,p′‐DDD and p,p′‐DDT), polychlorinated biphenyls (PCBs, PCB 28, 52, 101, 153, 138 and 180 congeners) and polybrominated diphenyl ethers (PBDEs, PBDE 47, 99, 100, 153 and 154 congeners) in 45 individual human milk samples collected from Konya City, Turkey. Average concentrations of ΣHCHs, ΣDDTs, ΣPCBs and ΣPBDEs were 22.62, 37.10, 104.95 and 67.34 ng/g lipid wt., respectively. No significant differences in investigated pollutants were found between primiparous and multiparous mothers. There was no correlation between levels of each group of pollutants in human milk and the age of mothers. Moreover, there was no significant difference in the levels of ΣDDTs, between mothers who have eaten fish more than once a week and those who consumed fish less than once. An analysis of the infant exposure to DDTs, HCHs and PCBs via mother's milk indicated that the estimated daily intakes of these pollutants were below the guideline proposed by the World Health Organization (WHO) and the Health Canada which means that there is definitely no concern on children health.     

Sediment hydrocarbon contamination at the site of the Baie Verte,Newfoundland, oil spill: Results of a Four Year Study

Sediments samples were taken at 3, 15, 27, and 39 months following a spill of diesel oil at Baie Verte, Newfoundland, to determine the effects of weathering on diesel oil trapped in the sediments and to attempt to develop a suitable method for extraction and analysis.Extraction was carried out using hexane, concentration was effected by a procedure modified from Junk et al. (1974) and analysis was completed within 18.0 min by high performance liquid chromatography (HPLC) using a bonded amino silane-(NH₂) column (5 μm, 5 mm × 25 cm) with hexane as mobile phase. A backflush cycle of 22.0 min using hexane and methl-t-butyl ether (90:10%) was performed to elute any polar compounds from the column.This class analysis by HPLC indicated a decrease in the amount of naphthalene, fluorene, phenanthrene and benzo[a]pyrene equivalents over time and at the conclusion of the study (39 months) no PAHs except for fluorene were found in the sediments from Baie Verte.     

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.     

Investigation on the Levels of Heavy Metals,Polycyclic Aromatic Hydrocarbons,and Polychlorinated Biphenyls in Sewage Sludge Samples and Ecotoxicological Testing

This article reports the levels of heavy metals, polycyclic aromatic hydrocarbons (PAHs), and polychlorinated biphenyls (PCBs) in sewage sludges taken from two wastewater treatment plants (WWTPs) in Konya (Turkey) as well as their toxicity. The concentrations of heavy metals, including Cd, Cr, Cu, Ni, Pb, Zn in sludge samples from plant #2 did not exceed the limits described in both Turkish and European Union (EU) regulations. The similar result was observed in samples obtained from plant #1, except for sludge taken in May 2010. The ΣPAHs concentration ranging from 960 to 7680 µg/kg dry matter shows that sewage sludges from plant #1 could be used for agricultural purpose. However, sewage sludges from plant #2 (ΣPAHs: 1077–17 509 µg/kg dry matter) was not suitable for using in agriculture. The concentrations of ΣPCBs in all investigated sludges from plant #1 (7.46–709.36 µg/kg dry matter) and plant #2 (14.12–788.47 µg/kg dry matter) were lower than the limits reported in Turkish and EU regulations. The probable sources of PAHs and PCBs in sludges were also determined. The ecotoxicological tests examined on Vibrio fischeri and Lepidium sativum organisms showed that sludges from plant #1 had no significant toxic effect, while sludges from plant #2 had acute toxic property. Finally, all the results showed that sewage sludges from plant #1 had potential for being used in agriculture.     

Biomagnification profiles of polycyclic aromatic hydrocarbons, alkylphenols and polychlorinated biphenyls in Tokyo Bay elucidated by δC and δN isotope ratios as guides to trophic web structure

Biomagnification profiles of polycyclic aromatic hydrocarbons (PAHs), alkylphenols, and polychlorinated biphenyls (PCBs) from the innermost part of Tokyo Bay, Japan were analyzed using stable carbon (δ¹³C) and nitrogen (δ¹⁵N) isotope ratios as guides to trophic web structure. δ¹⁵N analysis indicated that all species of mollusks tested were primary consumers, while decapods and fish were secondary consumers. Higher concentrations of PCBs occurred in decapods and fish than in mollusks. In contrast, concentrations of PAHs and alkylphenols were lower in decapods and fish than in mollusks. Unlike PCBs, whose concentrations largely increased with increasing δ¹⁵N (i.e. increasing trophic level), all PAHs and alkylphenols analyzed followed a reverse trend. Molecular weights of PAHs are lower than those of PCBs, therefore low membrane permeability caused by large molecular size is an unlikely factor in the “biodilution” of PAHs. Organisms at higher trophic levels may rapidly metabolize PAHs or they may assimilate less of them.     

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.     

Atmospheric Concentrations and Phase Partitioning of Polycyclic Aromatic Hydrocarbons in Izmir,Turkey

Ambient air polycyclic aromatic hydrocarbon (PAH) samples were collected at a suburban (n = 63) and at an urban site (n = 14) in Izmir, Turkey. Average gas‐phase total PAH (∑₁₄PAH) concentrations were 23.5 ng m^?3 for suburban and 109.7 ng m^?3 for urban sites while average particle‐phase total PAH concentrations were 12.3 and 34.5 ng m^?3 for suburban and urban sites, respectively. Higher ambient PAH concentrations were measured in the gas‐phase and ∑₁₄PAH concentrations were dominated by lower molecular weight PAHs. Multiple linear regression analysis indicated that the meteorological parameters were effective on ambient PAH concentrations. Emission sources of particle‐phase PAHs were investigated using a diagnostic plot of fluorene (FLN)/(fluorine + pyrene; PY) versus indeno[1,2,3‐cd]PY/(indeno[1,2,3‐cd]PY + benzo[g,h,i]perylene) and several diagnostic ratios. These approaches have indicated that traffic emissions (petroleum combustion) were the dominant PAH sources at both sites for summer and winter seasons. Experimental gas–particle partition coefficients (K_P) were compared to the predictions of octanol–air (K_OA) and soot–air (K_SA) partition coefficient models. The correlations between experimental and modeled K_P values were significant (r² = 0.79 and 0.94 for suburban and urban sites, respectively, p < 0.01). Octanol‐based absorptive partitioning model predicted lower partition coefficients especially for relatively volatile PAHs. However, overall there was a relatively good agreement between the measured K_P and soot‐based model predictions.     

Polycyclic aromatic hydrocarbons (PAHs) and organochlorine pesticides in water columns from the Pearl River and the Macao harbor in the Pearl River Delta in South China

Polycyclic aromatic hydrocarbons (PAHs) and organochlorine pesticides (OCPs) were measured in suspended particles and dissolved phase from the Baiertang water column and the Macao water column samples as collected from the Guangzhou channel of the Pearl River and the Macao harbor, where the sediments were heavily contaminated with organic pollutants. Total OCPs concentration varies from 23.4 to 61.7 ng/l in Baiertang water column and from 25.2 to 67.8 ng/l in Macao column, while total PAHs concentration varies from 987.1 to 2878.5 ng/l in the Baiertang water column and from 944.0 to 6654.6 ng/l in the Macao column. The vertical distribution profiles of pollutants and the partition of pollutants between particles and dissolved phases indicate that the sediments in Baiertang act as an important source of selected pollutants, and the pollutants in water of this region were mainly originated from the release and re-suspension of contaminants residing in the sediments. The sediments in Macao harbor act as a reservoir for organochlorine pesticides, such as DDTs mainly introduced by river inflow from Xijiang and PAHs input by brackish water from the Lingdingyang estuary. Combustion of fossil fuels and petroleum input are the main sources of PAHs in the Macao water column, while combustion of fossil fuels and coal is responsible for the PAHs in the Baiertang water column. The ratios of DDT/(DDD+DDE) for the Macao water column samples demonstrate that such chemicals were input into this region in recent times.     

Occurrence and distribution of organochlorine residues in surface sediments of the Candarli Gulf (Eastern Aegean)

The residual levels of organochlorine pesticides (OCPs) and polychlorinated biphenyls (PCBs) were determined in surface sediments collected from Candarli Gulf. Total concentrations of OCPs and PCBs in sediments ranged from 10.2 to 57.3 and 2.8 to 205 ng g⁻¹ dwt, respectively. DDTs in sediments were derived from the aged and weathered agricultural soils in 61% of the sampling stations while 39% of the sites originated from the recent DDT inputs. Their concentrations appeared to be relatively low by global standards and only sediments receiving the impact from the Bakircay River and petrochemical industry approached the sediment quality guidelines for PCBs and DDTs. Based on ERL/ERM guidelines, DDT and PCBs posed ecological risk to the bottom-dwelling consumers.     

Removal of Heavy Metals from Synthetic Mixture as well as Pharmaceutical Sample Via Cation Exchange Resin Modified with Rhodamine B: Its Thermodynamic and Kinetic Studies

A new sorbent was prepared by loading rhodamine B on Amberlite IR‐120. Various physico‐chemical parameters such as effects of adsorbate concentration, contact time, pH, and temperature on the sorption of the dye have been studied. Thermodynamic parameters (ΔH° and ΔS°) were also evaluated for the sorption of dye. Kinetic studies revealed that the sorption of the dye was best fit for pseudo‐second‐order kinetic. The metal ion uptake in different solvent systems has been explored through column studies. On the basis of distribution coefficient (K_d), some heavy metal ions of analytical interest from binary mixtures have been separated. The limit of detection (LOD) for the Ni²⁺ and Fe³⁺ metal ions was 0.81 and 0.60 µg L^?1, and the limit of quantification (LOQ) was found to be 2.72 and 2.0 µg L^?1. This sorbent has also been successfully applied in the analysis of multivitamin formulation. The applicability of the modified resin in the separation of heavy metals constituting real and synthetic samples has been explored.     

Effect of Co‐culture and Nutrients Supplementation on Bioremediation of Crude Petroleum Sludge

Ex‐situ bioremediation of real‐field crude petroleum sludge was evaluated to elucidate the role of co‐culture (bioaugmentation) and external nutrients supplementation (biostimulation) under anaerobic microenvironment. Maximum removal of total petroleum hydrocarbons (TPH) was observed by integrating biostimulation with bioaugmentation (R5, 44.01%) followed by bioaugmentation alone (R4, 34.47%), co‐substrate supplemented operations [R6, 23.36%; R3, 16.5%; R2, 9.88%] and control (R1, 4.36%). Aromatics fraction showed higher degradation in all the conditions studied. Fate of six selected polycyclic aromatic hydrocarbons (PAHs) was evaluated during bioremediation. Among these, four ring PAHs compounds showed good degradation by integration of biostimulation with bioaugmentation (R5) while bioaugmentation alone (R4) documented good degradation of three ring PAHs. Lower ring PAHs compounds showed good degradation with the application of biostimulation (R6). Fluorescent in situ hybridization (FISH) detected the presence of known PAHs degrading microorganisms viz., Bacillus, Pseudomonas, Acido bacteria, Sulphur reducing bacteria Firmicutes, etc. Application of biostimulation and bioaugmentation strategies alone or in combinations documented noticeable influence on the degradation of petroleum sludge.     

Selective Preconcentration of Trace Amounts of Cu(II) With Surface‐Imprinted Multiwalled Carbon Nanotubes

In this study, a new sorbent is synthesized using surface imprinting technique. Cu(II)‐imprinted multiwalled carbon nanotube sorbent (Cu(II)‐IMWCNT) is used as the solid phase in the solid‐phase extraction method. After the preconcentration procedure, Cu(II) ions are determined by high‐resolution continuum source atomic absorption spectrometry. A total of 0.1 mol L^?1 ethylenediaminetetraacetic acid (EDTA) is used to remove Cu(II) ions from the sorbent surface. The optimum experimental conditions for effective preconcentration of Cu(II), parameters such as pH, eluent type and concentration, flow rate, sample volume, sorbent capacity, and selectivity are investigated. The synthesized solid phase is characterized by Fourier transform infrared spectroscopy and scanning electron microscopy. The maximum adsorption capacities of Cu(II)‐IMWCNT and non‐imprinted solid phases are 270.3 and 14.3 mg g^?1 at pH 5, respectively. Under optimum experimental conditions for Cu(II) ions, the limit of detection is 0.07 μg L^?1 and preconcentration factor is 40. In addition, it is determined to be reusable without significant decrease in recovery values up to 100 adsorption–desorption cycles. Cu(II)‐IMWCNT have a high stability. To check the accuracy of the developed method, certified reference materials, and water samples are analyzed with satisfactory analytical results.     

An assessment of the pollutant status of surficial sediment in Cork Harbour in the South East of Ireland with particular reference to polycyclic aromatic hydrocarbons

Surface sediment from three polluted sites within Cork Harbour, Ireland, and from a relatively clean reference site were collected and analysed for polycyclic aromatic hydrocarbons (PAHs), polychlorinated biphenyls (PCBs), organochlorine pesticides (OCPs), brominated flame retardants (BFRs), organotins (OTs), and heavy metals. PAHs were determined to be the most abundant class of contaminant. Concentrations of the sum (Sigma) of the 21 PAHs measured from the Harbour sites (2877.70 ng g(-1), 1000.7 ng g(-1) and 924.40 ng g(-1) dry weight respectively) were significantly higher than that of the sediment from the reference site (528.30 ng g(-1) dry weight). An inner harbour site, Douglas being the more contaminated of the three harbour sites. A similar pattern was observed with the other contaminants however, these compounds, with the exception of the heavy metals, all tended to be detected at concentrations on or below detection limits.     

Removal of Ni(II) Using Cation Exchange Resins in Packed Bed Column: Prediction of Breakthrough Curves

Sorptive removal of Ni(II) from electroplating rinse wastewaters by cation exchange resin Dueolite C 20 was investigated at the temperature of 30°C under dynamic conditions in a packed bed. The effects of sorbent bed length 0.1–0.2 m, fixed flow rate 6 dm³ min^?1, and the initial rinse water concentration (C₀) 53.1 mg L^?1 on the sorption characteristics of Dueolite C 20 were investigated at an influent pH of 6.5. More than 94.5% of Ni(II) was removed in the column experiments. The column performance was improved with increasing bed height and decreasing the flow rate. The Thomas, Yoon–Nelson, Clark, and Wolborska models were applied to the experimental data to represent the breakthrough curves and determine the characteristic design parameters of the column. The sorption performance of the Ni(II) ions through columns could be well described by the Thomas, Yoon–Nelson, and Wolborska models at effluent‐to‐influent concentration ratios (C/C₀) >0.03 and <0.99. Among the all models, the Clark model showed the least average percentage time deviation. The sorptive capacity of electroplating rinse water using Ni(II) was found to be 45.98 mg g^?1.     

Sorption Behaviour of Phenols on Natural Sandy Aquifer Material during Flow‐through Column Experiments: The Effect of pH

Flow‐through column experiments were carried out to investigate the influence of pH on the sorption of three phenols (2‐methyl‐4, 6‐dinitrophenol, 2, 4, 6‐trichlorophenol, pentachlorophenol) onto a natural sandy aquifer material collected from a bank filtration site of River Elbe, Germany. For the phenols investigated, an increase in sorption (retardation) with decreasing pH is observed indicating a stronger sorption of the neutral species in comparison to that of the anions formed by dissociation. The anions of 2‐methyl‐4, 6‐dinitrophenol and 2, 4, 6‐trichlorophenol do not show significant sorption. On the contrary, pentachlorophenol showed sorption not only in neutral form but also in ionic form significantly which should be taken into account while assessing the fate and transport of such compound. A linear model based on the degree of protonation (calculated from pH and pK_a) can be used to resolve the apparent (observed) sorption coefficient (K_{d, app}) into its neutral (K_{d, n}) and ionised (K_{d, i}) components. Knowing pK_a, K_{d, n}, and K_{d, i} the apparent sorption coefficient for pH values other than experimentally investigated can be predicted.     

Optimization and Characterization of Tl(I) Adsorption onto Modified Ulmus carpinifolia Tree Leaves

Ulmus carpinifolia tree leaves were successfully used to remove Tl(I) from aqueous solution in a batch system. In order to improve the uptake capacity of sorbent, it was modified by various chemical agents such as NaOH, HNO₃, NH₃, NaCl, NaHCO₃, and CaCl₂. Among the modifiers, NaCl was the best. Equilibrium behavior of sorbent with Tl(I) was examined by the several isotherms. Considering modified U. carpinifolia equilibrium data fitted well to the Langmuir model with maximum capacity of 54.6 mg/g. The other isotherms such as: Freundlich and Dubinin‐Redushkevich (D‐R) models were also examined. The central composite design (CCD) was successfully employed for optimization of biosorption process. An empirical model was given through using response surface methodology. Also its validation was recognized by using relevant statistical tests such as ANOVA. The optimum conditions of biosorption: pH, m (amount of sorbent) and C (initial concentration) were found to be 7.9, 11.4 g/L, and 8.8 mg/L, respectively. On the other hand thermodynamic parameters: ΔG, ΔH, and ΔS were evaluated: the obtained results show that biosorption process was spontaneous and exothermic. Eventually, FT‐IR analysis confirmed that the main functional groups of sorbent have been involved through the biosorption process.