Biosorption of Hg(II) and Cu(II) by biomass of dried Sargassum fusiforme in aquatic solution
© Huang and Lin; licensee BioMed Central. 2015
Received: 29 September 2014
Accepted: 9 March 2015
Published: 17 March 2015
The biosorption of heavy metals Hg(II) and Cu(II) from aquatic solution by biomass of dried Sargassum fusiforme was studied in the paper. The Sargassum fusiforme was able to absorb appreciable amount of mercury and copper from the aquatic solutions within 60 min of contact time with the metal solution and exhibited high removal of mercury and copper at low equilibrium concentrations. The specific adsorption of both Hg(II) and Cu(II) increased at low concentration of biomass and decreased when biomass concentration exceeded 2.0 g/L. The binding of mercury followed Freundlich model while copper supported Langmuir isotherm for adsorption with their r2 values of 0.971 and 0.923, respectively. The maximum adsorption per unit masses of Sargassum fusiforme (mg/L) at equilibrium (qmax) for Hg(II) and Cu(II) were calculated to be 30.86 and 7.69 mg/g, respectively. The biosorption by Sargassum fusiforme was best described using a pseudo-second-order kinetic model for copper and mercury ions in solution in the study. The adsorption was pH dependent as the maximum mercury biosorption and copper adsorption was happened at solution pH of 8–10.
KeywordsBiosorption Sargassum fusiforme Mercury Copper
The heavy metal is among the most common pollutant found in industrial effluents. The major sources of pollution in the aquatic environment are industries such as paint, pulp and paper, oil refining, electrical, rubber, processing, fertilizer, pharmaceutical and battery manufacturing [1,2]. The major effects of mercury and copper poisoning manifest as neurological and renal disturbances as it can easily pass the blood–brain barrier. Environmental contamination with toxic heavy metals is a significant worldwide problem with their successive accumulation in the food chain and continued persistence in the ecosystem which will hurt human beings. Efforts have been made to remove toxic heavy metal from the wastewater and environment by using conserved technologies such as ion exchange or chemical precipitation, which are sometimes inefficient and expensive, particularly for removal of low concentrated heavy metal ions , and also leads to produce toxic sludge that adverse the economical feasibility of the treatment methods.
Indeed, many early studies have shown that nonliving biomass may be even more effective than living cells in sequestering metallic elements. Over the past two decades, much effort has been directed at identifying readily available biomass which, in its nonliving state, is capable of effectively removing heavy metals. It has been demonstrated that biosorption is a potential alternative to traditional treatment processes of metal ions removal. Biosorption is a property of certain types of inactive, dead biomass to bind and concentrate heavy metals from even very dilute aqueous solutions . Biomass exhibits this property, acting just as a chemical substance, as an ion exchange of biological origin. Research on biosorption is revealing that it is sometimes a complex phenomenon where the metallic species could be deposited in the solid biosorbent through different sorption processes of ion exchange, complexation, chelation, microprecipitation, etc.
In these years, the role of seagrass in removal of toxic metal ions from the polluted water have taken more importance as they have a high area-to-volume ratio and therefore provide a large contact area for metal binding . Small bacteria, algae, fungi and yeast have been well recognized for heavy metal removal . Up to date, the role of algae has received increased attention to years because of it are potential for application of environmental protection as well as recovery of heavy metals. The affinity with various algae species for binding of heavy metals shows different results . Metal ions with greater electro-negativity and smaller ionic radii are preferably absorbed by algae biomass . Metal accumulation capacity of algae biomass is sometimes higher than chemical sorbents therefore algae biomass may serve as an economically feasible to the existing physicochemical methods of metal removal of wastewaters. The major challenge to biosorption studies is to select the most promising biomass from a large pool of available and inexpensive biomaterials. Contributions to Sargassum fusiforme in the metal adsorption is of great concern .
In the present study, dried biomass of Sargassum fusiforme were used and characterized for its Cu(II) and Hg(II) removal potential from synthetic metal solution. The effect of pH, biomass concentration, initial metal concentration and contact time was studied for metal sorption procedure as well as heavy metal equilibrium sorption kinetics was made in lab.
The dry biomass of Sargassum fusiforme were purchased from Fuzhou Lantian limited Company, Fujian (China). It was powdered and sieved into less than 1 mm in diameter and dried at 80°C for 12 h with drying oven(01A, Suzhou sinovel oven manufacturing co., LTD). The characteristics of the Sargassum fusiforme were determined by F-Sorb type 3400 specific surfaces and pore diameter gauge(Beijing gold spectrum technology co., LTD). The surface BET on the algae was of means with 35-40 m2/g, total pore volume is of 50-70% and the pore structure is mesoporous material. The FTIR spectrum of the fresh and metal-loaded ones were made by the FTIR920(Tianjin topology instrument co., LTD). The SEM images of the fresh and metal-loaded ones were attained by SU3500(Hitachi High-Technologies Corporation).
Mercury and copper sorption experiments
Heavy metal solutions were prepared for diluting 200 mg/L of stock solutions, which were made by dissolving copper nitrate and mercury nitrate of analytical grade (Shanghai bo yiu biological technology co., LTD) in double distilled water. Metal sorption studies were carried out to evaluate the capacity of dry biomass of Sargassum fusiforme to adsorb metal ions from solutions. In batch ones, 100 mL of synthetic metal solutions having different concentrations (10,20,30,40, and 50 mg/L) of copper or mercury were placed in 250 ml Erlenmeyer flasks with a range of biomass concentrations(0.5,1.0,22.214.171.124,2.5, and 3.0 g/L) as biosorbent. Erlenmeyer flasks were kept under shaking at 120 rpm at 25°C. Samples were taken after 20-120 min and filtered and analyzed for final metal concentration (Cf) using ICP-AES (HK-2000, Huake Beijing tiancheng technology co., LTD) after an acid digestion .
To see the effect of pH on Hg(II) and Cu(II) removal, a range of pH (2–10) was adjusted to 0.1 M NaOH or 0.1 M HCl in 100 ml metal solutions containing fixed concentration of metal at 10 mg/L and biomass of 3.0 g/L followed by contact time of 60 min at rotation of 120 rpm. The metal adsorption(q) with Sargassum fusiforme and bioremoval efficiency(R) were calculated by the following formulae.
Where q = metal adsorption (mg/g); M = dry mass of Sargassum fusiforme(g); V = volume of initial metal solution used (L); R = bioremoval efficiency (%); Ci = initial concentration of metal in aquatic solution (mg/L); Cf = final concentration of metal in aquatic solution (mg/L) .
During biosorption, the equilibrium is established between absorbed metal ion on the Sargassum fusiforme(q) and unabsorbed metal ions in the solution(Cf). This equilibrium represented by Langmuir and Freundlich adsorption isotherms, are widely used to analyze data for wastewater treatment application . Langmuir equation, which is valid for monolayer sorption onto a surface, with identical sites was given by Eq. 3.
Where qmax(mg/g) is the maximum amount of the metal ion per unit weights of algae to form a complete monolayer on the surface bound at high Cf(mg/L), and b is a constant related to the affinity of the binding sites(mg/L), qmax represents a practical limiting adsorption capacity when the surface is fully covered with metal ions and assists in the comparison of adsorption performance . The qmax and b can be determined from the liner plot of Cf/q versus Cf. The empirical Freundlich equation based on sorption on a heterogeneous surface is given below by Eq. 4.
The k and n parameters are the constants of the Freundlich isotherm. The k and n are indicators of adsorption capacity and adsorption intensity, respectively. The Eq.4 can be linearized in logarithmic forms and Freundlich constants can be determined by the plot. Freundlich isotherm is also more widely used as it provides no information on the monolayer adsorption capacity .
The experimental biosorption kinetic data was modeled using the pseudo-first-order (Eq.5), and pseudo-second-order models (Eq.6). The linear pseudo-first-order model can be represented by the following equation:
Where K2 (g*mg−1*min−1) is the equilibrium rate constant of pseudo-second-order .
Results and discussion
Effect of pH solution
It was observed that Hg(II) and Cu(II) adsorption was less than 10% at pH 2. Enhance adsorption of Hg(II) and Cu(II) ions at higher pH was observed which coincides with earlier findings where in most cases the removal efficiency increased steadily with rise in pH . The adsorption of metal ions was lower at low pH because of high concentration of protons in the solution which competed with metal ions in forming a bond between the active sites on the surface of the algae biomass . Selective sorption of specific metals due to distinct pH optima for their sorption may be due to the chemical composition of cell surfaces. A distinct relationship between pH of aquatic metal solutions and involvement of functional group in binding of Hg(II) and Cu(II) onto Sargassum fusiforme maxima was observed with the involvement of functional groups such as carboxyl, phosphate and hydroxyl .
Contact time determination
The Sargassum fusiforme biomass showed rapid biosorption at first 60 min. It has been reported that the sorption of heavy metal ions by algae followed mechanism where the metal ion is physically or chemically taken up onto the surface of the algae . In this case, since the algae were dried and biological functions were no longer active, the sorption could only take place on the cell surface. The increase in Hg(II) and Cu(II) adsorbed by increasing biomass was also expected as a result of increase in available area-to-volume ratio and therefore providing a large contact area for heavy metal binding .
Hg(II) adsorption was increased to 71% by increasing biomass concentration on 0 to 3.0 g/L in 10 mg/L of mercury containing synthetic solutions whereas, same trend was observed in case of Cu(II) with the increase of 90%. The Sargassum fusiforme biomass displayed its equilibrium for Hg(II) removal of 3.0 g/L of biomass concentration whereas, a continuous increase in Cu(II) removal of increasing biomass concentration was observed of 3.0 g/L. Metal adsorption studies from solution mass balance revealed a decline in sorption of Hg(II) and Cu(II) respectively by increasing biomass from 0 to 3.0 g/L after 60 min of contact time. The other probable explanations for such a relationship between biomass concentration and adsorption may be limited availability of metal, increased electrostatic interactions between binding sites and reduced mixing at higher biomass concentration [21,22].
The FTIR and SEM analysis
Langmuir and Freundlich parameters for the sorption of the test metals by Sargassum fusiforme
The sorption isotherm is the relationship between equilibrium concentration on the solution and equilibrium concentration of solute in the sorbent at constant temperature where either Freundlich or Langmuir model can describe the biosorption equilibrium of copper and mercury . An extremely high r2 value of Freundlich isotherm for Hg(II) sorption indicated that ion exchange interaction takes place between metal ion and the biosorbent, while Cu(II) follows Langmuir isotherm and thus supported physicochemical interactions with each other.
First and second order adsorption rate constants for Hg(II) and Cu(II)
K 1 (min −1 )
K 2 (g*mg −1 *min −1 )
The goal of the study was to explore and find out the potential use of algae biomass as a low cost sorbent for the removal of heavy metals from aquatic solutions. The heavy metals Hg(II) and Cu(II) from aquatic solution was able to be dealt with dried Sargassum fusiforme. The seagrass adsorbed appreciable amount of mercury and copper from the aquatic solutions within 60 min at low equilibrium concentrations. The specific adsorption of both Hg(II) and Cu(II) increased at low concentration while decreased when biomass concentration exceeded 2.0 g/L. The binding of mercury followed Freundlich model but copper supported Langmuir isotherm for adsorption with their r2 values of 0.971 and 0.923, respectively. The maximum adsorption per unit masses of Sargassum fusiforme (mg/L), at equilibrium (qmax) for Hg(II) and Cu(II) were calculated to be 30.86 and 7.69 mg/g respectively. The adsorption was pH dependent as the maximum mercury biosorption utilized at pH 8 and 10 and Cu(II) adsorption was at pH 8 and 10. The biosorption by Sargassum fusiforme was best described using a pseudo-second-order kinetic model for copper and mercury ions in solution in the study. The present paper emphasizes the Sargassum fusiforme is an ideal candidate and can be designed as a practical and economical process for wastewater treatment polluted by heavy metals.
We greatly thank Chen Guantong from FAU for providing researching materials in this investigation. We are also grateful to Zhang Danfeng for the helpful comments and linguistic revision of the manuscript. This work was supported by grants from the ministry of education from Hubei province, People’s Republic of China(project No. Q20122506).
- Rezaee A, Ramavandi B, Ganati F. Biosorption of mercury by biomass of filamentous algae Spirogyra species. J Biol Sci. 2006;6(4):695–700.View ArticleGoogle Scholar
- Khodaverdiloo H, Samadi A. Batch equilibrium study on sorption, desorption, and immobilisation of cadmium in some semi-arid zone soils as affected by soil properties. Soil Res. 2011;49:444–54.View ArticleGoogle Scholar
- Lu WB, Shi JJ, Wang CH, Chang JS. Biosorption of lead, copper and cadmium by indigenous isolate Enterobacter sp. Processing high heavy metal resistance. J Hazard Mater. 2006;134:80–6.View ArticleGoogle Scholar
- Rezaee A, Ramavandi B, Ganati F. Equilibrium and spectroscopic studies on biosorption of mercury by algae biomass. Pak J Biol Sci. 2006;9(4):777–82.View ArticleGoogle Scholar
- Pandiyan S, Mahendradas D. Application of bacteria to remove Ni(II) Ions from aqueous solution. Eur J Sci Res. 2011;52:345–58.Google Scholar
- Ekmekyapar F, Aslan A, Bayhan YK, Cakici A. Biosorption of copper (II) by nonliving lichen biomass of Cladonia rangiformis hoffm. J Hazard Mater. 2006;B137:293–8.View ArticleGoogle Scholar
- Zouboulis AI, Loukidou MX, Matis KA. Biosorption of toxic metals from aqueous solution by bacterial strains isolated from metal-polluted soils. Process Biochem. 2004;39:909–16.View ArticleGoogle Scholar
- Anjana K, Kaushik A, Kiran B, Nisha R. Biosorption of Cr(VI) by immobilized biomass of two indigenous strains of cyanobacteria isolated from metal contaminated soil. J Hazard Mater. 2007;148:383–6.View ArticleGoogle Scholar
- Naik UC, Srivastava S, Thakur IS. Isolation and characterization of Bacillus cereus IST105 from electroplating effluent for detoxification of hexavalent chromium. Environ Sci Pollut Res Int. 2011;19:3005–14.View ArticleGoogle Scholar
- Vijayaraghavan K, Jegan J, Palanivenu K, Velan M. Biosorption of cobalt(II)and nickel(II) by seaweeds: batch and column studies. Sep Purif Technol. 2005;44:53–9.View ArticleGoogle Scholar
- Ok YS, Yang JE, Zhang YS, Kim SJ, Chung DY. Heavy metal adsorption by a formulated zeolite-Portland cement mixture. J Hazard Mater. 2007;147:91–6.View ArticleGoogle Scholar
- Kaewsarn P, Yu Q. Cadmium (II) removal from aqueous solutions by pretreated biomass of marine alga Padina sp. Environ Pollut. 2001;112:209–13.View ArticleGoogle Scholar
- Chatterjee SK, Bhattacharjee I, Chandra G. Biosorption of heavy metals from industrial waste water by Geobacillus thermode nitrificans. J Hazard Mater. 2010;175:117–25.View ArticleGoogle Scholar
- Lodeiro P, Barriada JL, Herrero R, Sastre deVicente ME. The marine macroalga Cystoseira baccata as biosorbent for cadmium (II) and lead (II) removal: kinetic and equilibrium studies. Environ Pollut. 2006;142:264–73.View ArticleGoogle Scholar
- Vilar VJP, Botelho CMS, Boaventura RAR. Lead uptake by algae Gelidium and composite material particles in a packed bed column. Chem Eng J. 2008;144:420–30.View ArticleGoogle Scholar
- Costodes VCT, Fauduet H, Porte C, Delacroix A. Removal of Cd(II) and Pb(II)ions from aqueous solutions by adsorption onto sawdust of Pinus sylvestris. J Hazard Mater. 2003;105:121–42.View ArticleGoogle Scholar
- Pabst MW, Miller CD, Dimkpa CO, Anderson AJ, McLean JE. Defining the surface adsorption and internalization of copper and cadmium in a soil bacterium Pseudomonas putida. Chemosphere. 2010;81:904–10.View ArticleGoogle Scholar
- Sari A, Tuzen M. Biosorption of Pb(II) and Cd(II) from aqueous solution using green alga (Ulva lactuca) biomass. J Hazard Mater. 2008;152:302–8.View ArticleGoogle Scholar
- Oliveira SM, Pessenda LC, Gouveia SE, Favaro DI. Heavy metal concentrations in soils from a remote oceanic island, Fernando de Noronha. Braz An Acad Bras Cienc. 2011;83:1193–206.View ArticleGoogle Scholar
- Pardo R, Herguedas M, Barrado E, Vega M. Biosorption of cadmium, copper, lead and zinc by inactive biomass of Pseudomonas putida. Anal Bioanal Chem. 2003;376:26–32.Google Scholar
- Wang XS, Qin Y. Removal of Ni(II), Zn(II) and Cr(VI) from aqueous solution by Alternanthera philoxeroides biomass. J Hazard Mater. 2006;138:582–8.View ArticleGoogle Scholar
- Xiong J, He Z, Liu D, Mahmood Q, Yang X. The role of bacteria in the heavy metals removal and growth of Sedum alfredii Hance in an aqueous medium. Chemosphere. 2008;70:489–94.View ArticleGoogle Scholar
- Mata YN, Blazquez ML, Ballester A, Gonzalez F, Munoz JA. Characterization of the biosorption of cadmium, lead and copper with the brown alga Fucus vesiculosus. J Hazard Mater. 2008;158:316–23.View ArticleGoogle Scholar
This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.