Biosorption of Cadmium from Aqueous Solution by Shell Dust of the Fresh Water Snail Melanoides tuberculata

ABSTRACT The metal bioadsorption potential of shell dust of the freshwater snail Melanoides tuberculata (MTSD) was evaluated under laboratory conditions using cadmium as a model metal. As bioadsorbent, MTSD exhibited a biosorption capacity of 27.03 mg g^?1 at pH 6, indicating potential to remove cadmium from aqueous solution. The adsorption data fit more to the Langmuir (R² = 0.998) equation than the Freundlich (R² = 0.761) equation at equilibrium condition. The kinetics of biosorption followed the pseudo-second-order model (R² = 0.999) better than the Lagergren model (R² = 0.676), as was evident from the regression analysis. The presence of calcium ions appears to have facilitated ion exchange with cadmium along with the binding of different functional groups, as revealed through Fourier transform infrared (FT-IR) analysis. It is apparent from these observations that MTSD can act as low-cost and efficient bioadsorbent for cadmium bioremediation from aquatic habitats. Use of the shells of M. tuberculata for metal biosorption will promote the utility of a waste material of biological origin for bioremediation of heavy metals such as cadmium.     

Equilibrium and kinetic studies on biosorption potential of charophyte biomass to remove heavy metals from synthetic metal solution and municipal wastewater

The risk of heavy metal contamination in domestic water causes serious health and environmental problems. Biosorption has been considered as an efficient and alternative way for treatment of heavy metal–contaminated wastewater. The potentials of dried charophytes, Chara aculeolata and Nitella opaca, to biosorb lead (Pb), cadmium (Cd), and zinc (Zn) from synthetic solutions and municipal wastewater were investigated. The efficiency of metal removal was studied under varied conditions in different sorbent dosages, pH, and contact times. Biosorption isotherm and kinetics were used to clarify heavy metal preference and biosorption mechanism. C. aculeolata and N. opaca performed well in the biosorption of all three metal ions, with preference towards Pb, followed by Cd and Zn, in the single-metal solutions. Pb adsorption onto algal biomass followed first-order rate kinetics (N. opaca) and intraparticle diffusion (C. aculeolata and N. opaca). These results indicated physical adsorption process between Pb ions and both algal biomasses. Cd and Zn biosorption kinetics fitted the second-order rate model, indicating chemical adsorption between metal ions and both algae. The experimental data of three-metal biosorption fitted well to Langmuir isotherm model, suggesting that the metal ion adsorption occurred in a monolayer pattern on a homogeneous surface. C. aculeolata exhibited slightly higher maximum uptake of Pb, Cd, and Zn (105.3 mgPb/g, 23.0 mgCd/g, 15.2 mgZn/g) than did N. opaca (104.2 mgPb/g, 20.5 mgCd/g, 13.4 mgZn/g). In multi-metal solutions, antagonistic effect by metal competition was observed. The ability of charophytes to remove Pb and Zn was high in real municipal water (81–100%). Thus, the charophytic biomass may be considered for the treatment of metal contamination in municipal wastewater.     

Biosorption Behavior of Ciprofloxacin onto Enteromorpha prolifera: Isotherm and Kinetic Studies

The studies aimed at the feasibility of using Enteromorpha prolifera for the removal of ciprofloxacin from aqueous solutions. Batch experiments were carried out for the biosorption of ciprofloxacin onto Enteromorpha prolifera. The factors affecting the biosorption process such as the initial concentration, dosage, pH and the contact time were studied. Enteromorpha prolifera exhibited a maximum biosorption capacity of 21.7 mg/g. The pseudo-second-order kinetic model described the ciprofloxacin biosorption process with a good fitting. The optimum pH of ciprofloxacin adsorbed by Enteromorpha prolifera was 10. Biosorption equilibrium studies demonstrated that the biosorption followed Freundlich isotherm model, which implied a heterogeneous biosorption phenomenon.     

Fish (Labeo rohita) Scales as Potential Low-Cost Biosorbent for Removal of Malachite Green from Aqueous Solutions

The feasibility of using fish (Labeo rohita) scales as low-cost biosorbent for the removal of hazardous Malachite Green (MG) dye from aqueous solutions was investigated. Employing a batch experimental setup, the effect of operational parameters such as biosorbent dose, initial solution pH, contact time, and temperature on the dye removal process was studied. The equilibrium biosorption data followed both Langmuir and Freundlich isotherm models, whereas the experimental kinetic data fitted well to the pseudo-second-order kinetic model. Thermodynamic study indicated spontaneous and endothermic nature of the biosorption process. The results suggest that fish scales could be used as an effective biosorbent for removal of MG dye from aqueous solutions.     

Experimental and theoretical approaches for Cd(II) biosorption from aqueous solution using Oryza sativa biomass

Biomass of Oryza sativa (OS) was tested for the removal of Cd(II) ions from synthetic and real wastewater samples. Batch experiments were conducted to investigate the effects of operating parameters on Cd(II) biosorption. Fourier transform infrared spectroscopy, scanning electron microscopy, and energy-dispersive x-ray spectroscopy were used to examine the surface characteristics of the Cd(II)-loaded biomass. The maximum removal efficiency of Cd(II) was 89.4% at optimum pH 6.0, biosorbent dose 10.0 g L^?1, initial Cd(II) 50 mg L^?1, and biosorbent particle size 0.5 mm. The applicability of Langmuir and Freundlich isotherms to the sorbent system implied the existence of both monolayer and heterogeneous surface conditions. Kinetic studies revealed that the adsorption process of Cd(II) followed the pseudo-second-order model (r2: 0.99). On the theoretical side, an adaptive neuro-fuzzy inference system (ANFIS) was applied to select the operating parameter that mostly influences the Cd(II) biosorption process. Results from ANFIS indicated that pH was the most influential parameter affecting Cd(II) removal efficiency, indicating that the biomass of OS was strongly pH sensitive. Finally, the biomass was confirmed to adsorb Cd(II) from real wastewater samples with removal efficiency close to 100%. However, feasibility studies of such systems on a large-scale application remain to be investigated.     

Application of a novel phyco-composite biosorbent for the biotreatment of aqueous medium polluted with manganese ions

A composite phyco-biomass including four different marine macroalgae species (Chaetomorpha sp., Polysiphonia sp., Ulva sp., and Cystoseira sp.) was evaluated as a novel biosorbent for the biosorption of manganese ions from aqueous solution. The experimental studies were performed to optimize the operational factors including solution pH, biosorbent amount, initial manganese concentration, and reaction time in a batch-mode biosorption system. The removal yield of the biosorbent for manganese ions increased with increasing pH, manganese ion concentration, and reaction time, while it decreased as the biosorbent dose increased. The obtained kinetic data indicated that the removal of manganese ions by the biosorbent was best described by the pseudo-second-order model and the pore diffusion also contributed to the biosorption process. The results of isotherm and thermodynamic studies showed that the Freundlich model represented the biosorption equilibrium data well and this biotreatment system was feasible, spontaneous, and physical. The maximum manganese uptake capacity of used biosorbent was found to be 55.874 mg g^?1. Finally, a single-stage batch manganese biosorption system was designed and its kinetic performance was evaluated. All these findings revealed that the prepared composite macroalgae biosorbent has a fairly good potential for the removal of manganese ions from the aqueous medium.     

Bioremediation potential of a widespread industrial biowaste as renewable and sustainable biosorbent for synthetic dye pollution

In this study, a model synthetic azo dye (Basic red 46) bioremoval by Carpinus betulus sawdust as inexpensive, eco-friendly, and sustainable biosorbent from aqueous solution was examined in a batch biosorption system. The effective environmental parameters on the biosorption process, such as the value of pH, amount of biosorbent, initial dye concentration and contact time were optimized using classical test design. The possible dye-biosorbent interaction was determined by Fourier Transform Infrared Spectroscopy (FTIR) and Scanning Electron Microscopy (SEM). The equilibrium, thermodynamic, and kinetic studies for the biosorption of Basic red 46 onto the sawdust biomass were performed. In addition, a single-stage batch dye biosorption system was also designed. The dye biosorption yield of biosorbent was significantly influenced by the change of operating variables. The experimental data were best described by the Freundlich isotherm model and both the pseudo-first-order kinetic and the pseudo-second-order kinetic models. Thermodynamic research indicated that the biosorption of dye was feasible and spontaneous. Based on the Langmuir isotherm model, the biosorbent was found to have a maximum biosorption potential higher than many other biosorbents in the literature (264.915?mg g^?1). Thus, this investigation presents a novel green option for the assessment of waste sawdust biomass as a cheap and effective biosorbent material.     

Taguchi DoE methodology for modeling of synthetic dye biosorption from aqueous effluents: parametric and phenomenological studies

Abstract

Biosorption technology has been acknowledged as one of the most successful treatment approaches for colored industrial effluents. The problems such as its high manufacturing cost and poor regeneration capability in the use of activated carbon as a biosorbent have prompted the environmental scientists to develop alternative biosorbent materials. In this context, as a sustainable green generation alternative biosorbent source, the discarded seed biomass from pepper (Capsicum annuum L.) processing industry was explored for the biotreatment of colored aqueous effluents in this study. To test the wastewater cleaning ability of biosorbent, Basic red 46 was selected as a typical model synthetic dye. Taguchi DoE methodology was employed to study the effect of important operational parameters, contact time, pH and synthetic dye concentration, on the biosorption process and to develop a mathematical model for the estimation of biosorption potential of biosorbent. The percentage contribution of each of these process variables on the dye biosorption was found to be 19.31%, 41.39%, and 38.74%, respectively. The biosorption capacity under the optimum environmental conditions, contact time of 360?min, pH of 8 and dye concentration of 30?mg L^?1, was estimated to be 92.878?mg g^?1 (R²: 99.45). This value was very close to the experimentally obtained dye removal performance value (92.095?mg g^?1). These findings indicated the high ability of Taguchi DoE technique in the optimization and simulation of dye biosorption system. The kinetic and equilibrium modeling studies showed that the pseudo-second-order and Langmuir models were the best models for the elucidation of dye removal behavior of biosorbent. The thermodynamic studies displayed that the dye biosorption was a feasible, spontaneous and exothermic process. This parametric and phenomenological survey revealed that the discarded pepper seed biomass can be introduced as a potential and efficient biosorbent for the bioremediation of colored industrial effluents.     

Nickel(II) biosorption by <Emphasis Type="Italic">Rhodotorula glutinis</Emphasis>

The present study reports the feasibility of using Rhodotorula glutinis biomass as an alternative low-cost biosorbent to remove Ni(II) ions from aqueous solutions. Acetone-pretreated R. glutinis cells showed higher Ni(II) biosorption capacity than untreated cells at pH values ranging from 3 to 7.5, with an optimum pH of 7.5. The effects of other relevant environmental parameters, such as initial Ni(II) concentration, shaking contact time and temperature, on Ni(II) biosorption onto acetone-pretreated R. glutinis were evaluated. Significant enhancement of Ni(II) biosorption capacity was observed by increasing initial metal concentration and temperature. Kinetic studies showed that the kinetic data were best described by a pseudo-second-order kinetic model. Among the two-, three-, and four-parameter isotherm models tested, the Fritz-Schluender model exhibited the best fit to experimental data. Thermodynamic parameters (activation energy, and changes in activation enthalpy, activation entropy, and free energy of activation) revealed that the biosorption of Ni(II) ions onto acetone-pretreated R. glutinis biomass is an endothermic and non-spontaneous process, involving chemical sorption with weak interactions between the biosorbent and Ni(II) ions. The high sorption capacity (44.45 mg g⁻¹ at 25°C, and 63.53 mg g⁻¹ at 70°C) exhibited by acetone-pretreated R. glutinis biomass places this biosorbent among the best adsorbents currently available for removal of Ni(II) ions from aqueous effluents.     

Exploring the Cadmium Tolerance and Removal Capability of a Filamentous Fungus Fusarium solani

Abstract

Cadmium is one of the most toxic contaminant causing many problems to human health and the environment. These days the world is moving toward ecofriendly and efficient techniques to remove the pollutant from the wastewater. The present study aims to investigate the tolerance of Fusarium solani toward cadmium (Cd), nickel (Ni), and lead (Pb). Maximum tolerance was observed with Cd. Cadmium removal ability of F. solani was examined from contaminated PDB medium. pH, initial concentration and time optimization for maximum removal of Cd by F. solani was also studied. The maximum removal (92.4%) was recorded at initial concentration of 50?mg/L after 144?h of incubation. Cadmium exposure increased the level of glutathione (GSH) and oxidized glutathione (GSSG) contents and the activity of catalase (CAT) in F. solani. Fourier-transform infrared spectroscopy (FTIR) analysis indicated the involvement of the different surface functional group in biosorption of Cd while Scanning Electron Microscopy coupled with Energy Dispersive Spectroscopy (SEM-EDS) analysis revealed the presence of Cd on the surface of fungal cell. The changes observed in compositions of S, P, and Cd using EDS analysis on biomass surface indicated the precipitation of Cd as CdS and Cd₃(PO₄)₂. The XRD analysis revealed the presence of Cd₃(PO₄)₂ on mycelia surface of F. solani.     

Morphophysiological responses and programmed cell death induced by cadmium in <Emphasis Type="Italic">Genipa americana</Emphasis> L. (Rubiaceae)

Cadmium (Cd) originating from atmospheric deposits, from industrial residues and from the application of phosphate fertilizers may accumulate in high concentrations in soil, water and food, thus becoming highly toxic to plants, animals and human beings. Once accumulated in an organism, Cd discharges and sets off a sequence of biochemical reactions and morphophysiological changes which may cause cell death in several tissues and organs. In order to test the hypothesis that Cd interferes in the metabolism of G. americana, a greenhouse experiment was conducted to measure eventual morphophysiological responses and cell death induced by Cd in this species. The plants were exposed to Cd concentrations ranging from 0 to 16 mg l⁻¹, in a nutritive solution. In TUNEL reaction, it was shown that Cd caused morphological changes in the cell nucleus of root tip and leaf tissues, which are typical for apoptosis. Cadmium induced anatomical changes in roots and leaves, such as the lignification of cell walls in root tissues and leaf main vein. In addition, the leaf mesophyll showed increase of the intercellular spaces. On the other hand, Cd caused reductions in the net photosynthetic rate, stomatal conductance and leaf transpiration, while the maximum potential quantum efficiency of PS2 (Fv/Fm) was unchanged. Cadmium accumulated in the root system in high concentrations, with low translocation for the shoot, and promoted an increase of Ca and Zn levels in the roots and a decrease of K level in the leaves. High concentrations of Cd promoted morphophysiological changes and caused cell death in roots and leaves tissues of G. americana.     

The Role of CEC and pH in Cd Retention from Soils of North of Iran

Cadmium (Cd) is a critical environmental chemical in which sorption reactions control its entry into soil solution. The aim of the present study was to evaluate Cd sorption characteristics of some soils of the northern part of Iran with a wide range of physicochemical properties. Duplicates of each sample were equilibrated with solutions containing 5 to 500 mg Cd L^?1 with 0.01 M CaCl₂ as background solution. The quantity of Cd retention was calculated as the difference between initial and equilibrated Cd concentration. Sorption isotherms including Freundlich, Langmuir, Temkin, Dubinin-Radushkevich, and Redlich-Peterson were used to evaluate the behavior of Cd sorption. Cadmium sorption data were well fitted to Langmuir, Freundlich, and Redlich-Peterson isotherms. The constant of Freundlich equation (k_F ) and adsorption maxima (b_L ) of Langmuir equation were related to pH and cation exchange capacity (CEC). The maximum buffering capacity (K_d ) was significantly correlated with pH (R² = 0.52, p ≤ 0.001) and calcium carbonate equivalent (CCE) (R² = 0.63, p ≤ 0.001). Redlich-Peterson constants (k_RP and a_RP ) were significantly correlated with pH (R² k_RP = 0.30, p ≤ 0.007) and (R² a_RP = 0.27, p ≤ 0.012). It seemed that pH, CEC, and CCE were the main soil properties regulating Cd retention behavior of the studied soils.     

The Influence of pH on the Cadmium-Repressed Growth of the Alga Coelastrum proboscideum

The inhibition of growth by different concentrations of CdCl₂ in the range 4,5 × 10^?7 to 5.6 × 10^?7M was studied in the green alga Coelastrum proboscideum Bohlin in inorganic media at pH 4.3, 5.3 and 6.2. The factorial destgn of the experiments was evaluated as an analysis of 2² factors. Below pH 4.0 and above pH 6.5 growth was depressed without adding Cd. Cd concentrations exceeding 5.6 × 10^?8M reduced algal growth significantly with a 50% inhibition at 5.6 × 10^?7M Cd. The Cd concentration of 5.6 × 10^?7M was less toxic at pH 6.2 than at pH 5.3 and 4.3, thus revealing a negative interaction between protons and Cd.     

THE INFLUENCE OF pH ON ALGAL CELL MEMBRANE PERMEABILITY AND ITS IMPLICATIONS FOR THE UPTAKE OF LIPOPHILIC METAL COMPLEXES1

Uptake of lipophilic metal complexes by freshwater algae has recently been shown to be pH dependent. Here we look at different physiological aspects that could influence the diffusion of the lipophilic Cd complex, Cd(diethyldithiocarbamate)₂⁰ (Cd(DDC)₂⁰), into algal cells at different exposure pH values. Changes in cell membrane permeability were assessed as a function of pH for three species of green algae [Chlamydomonas reinhardtii P. A. Dang., Pseudokirchneriella subcapitata (Korshikov) Hindák, and Chlorella fusca var. vacuolata Shihira et R. W. Kraus] using two neutral, nonionic probes, fluorescein diacetate (FDA) and D‐sorbitol. In parallel experiments, we exposed algae to inorganic Cd or to Cd(DDC)₂⁰ and monitored Cd intracellular metal distribution, together with phytochelatin synthesis. For the three algal species acclimated at pH 5.5 (w/wo DDC 1 μM) and exposed at this pH, their permeability to FDA and D‐sorbitol was consistently lower than for algae growing at pH 7.0 and exposed at this pH (P < 0.001). The ratio of the FDA hydrolysis rate measured at pH 7.0 with respect to the rate measured at pH 5.5 (both in the presence of DDC) correlated with the ratio of the Cd(DDC)₂⁰ initial internalization rate constant obtained at pH 7.0 versus that obtained at pH 5.5 (three algae species, n = 9, r = 0.85, P = 0.004). Our results strongly suggest that acidification affects metal availability to algae not only by proton inhibition of facilitated metal uptake but also by affecting membrane permeability.     

Cadmium biosorption properties of the metal‐resistant Ochrobactrum cytisi Azn6.2

The aim of this work was to establish the conditions for using Ochrobactrum cytisi Azn6.2 as a metal biosorbent. Azn6.2 is a novel strain from the legume symbiont O. cytisi that has been isolated from nodules of Medicago polymorpha plants grown on heavy metal‐polluted soils. Compared with the strain ESC1, Azn6.2 showed some biochemical differences, as well as antibiotic susceptibility, Azn6.2 was multi‐resistant to heavy metals, such as Cu, Cd and Zn, and bacterial pellets were able to biosorb high amounts of Cd and Zn. As shown by scanning electron microscopy coupled to energy dispersive X‐ray, most of Cd was attached to the cell surface. Optimal conditions for Cd biosorption were established, being 1 mM Cd ions in solution and 2 h of contact with the biosorbent at room temperature. At these conditions, maximal Cd loading capacity reached 32–34 mg/g. Cd desorption from bacterial pellets was achieved after washing with EDTA or, at higher efficiency, at pH 1.0. These results indicated that biosorption/desorption on O. cytisi Azn6.2 biomass should be a cost‐effective method for Cd recovery from contaminated solutions.     

Biosorption of Cd(II) and Pb(II) onto brown seaweed, Lobophora variegata (Lamouroux): kinetic and equilibrium studies

The present work deals with the biosorption performance of raw and chemically modified biomass of the brown seaweed Lobophora variegata for removal of Cd(II) and Pb(II) from aqueous solution. The biosorption capacity was significantly altered by pH of the solution delineating that the higher the pH, the higher the Cd(II) and Pb(II) removal. Kinetic and isotherm experiments were carried out at the optimal pH 5.0. The metal removal rates were conspicuously rapid wherein 90% of the total sorption occurred within 90 min. Biomass treated with CaCl₂ demonstrated the highest potential for the sorption of the metal ions with the maximum uptake capacities i.e. 1.71 and 1.79 mmol g⁻¹ for Cd(II) and Pb(II), respectively. Kinetic data were satisfactorily manifested by a pseudo-second order chemical sorption process. The process mechanism consisting of both surface adsorption and pore diffusion was found to be complex. The sorption data have been analyzed and fitted to sorption isotherm of the Freundlich, Langmuir, and Redlich–Peterson models. The regression coefficient for both Langmuir and Redlich–Peterson isotherms were higher than those secured for Freundlich isotherm implying that the biosorption system is possibly monolayer coverage of the L. variegata surface by the cadmium and lead ions. FT-IR studies revealed that Cd(II) and Pb(II) binding to L. variegata occurred primarily through biomass carboxyl groups accompanied by momentous interactions of the biomass amino and amide groups. In this study, we have observed that L. variegata had maximum biosorption capacity for Cd(II) and Pb(II) reported so far for any marine algae. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Interaction of Pb and Cd with gum kondagogu (Cochlospermum gossypium): A natural carbohydrate polymer with biosorbent properties

Gum kondagogu (Cochlospermum gossypium), an exudates tree gum from India was explored for its potential to decontaminate toxic metals (Pb²⁺ and Cd²⁺). Optimum biosorption of metals were determined by investigating the contact time, pH, initial concentration of metal ions and biosorbent dose at 25 ± 2 °C. The maximum metal biosorption capacity for gum kondagogu was observed for Pb²⁺ (48.52 mg g⁻¹) and Cd²⁺ (47.48 mg g⁻¹) as calculated by Langmuir isotherm model. Kinetic studies showed that the biosorption rates could be described by pseudo-second-order expression. The metal interactions with biopolymer were assessed by FT-IR, SEM–EDXA and XPS analysis. Results based on these techniques suggest that mechanism of metal binding by the biopolymer involves micro-precipitation, ion-exchange and metal complexation.     

UPTAKE OF CADMIUM BY FRESHWATER GREEN ALGAE: EFFECTS OF PH AND AQUATIC HUMIC SUBSTANCES1

The effects of humic substances and low pH on short‐term Cd uptake by Pseudokirchneriella subcapitata (Korshikov) Hindak and Chlamydomonas reinhardtii Dang were investigated under defined exposure conditions. The uptake experiments were run in the presence of either a synthetic organic ligand (nitrilotriacetate) or natural organic ligands (Suwannee River fulvic or humic acid). An ion‐exchange method was used to measure the free Cd²⁺ concentrations in the exposure solutions. At pH 5, measured free Cd²⁺ concentrations agreed with estimations made using the geochemical equilibrium model WHAM, but at pH 7 the model overestimated complexation by both Suwannee River fulvic and humic acids compared with the ion‐exchange measurements. Consistent with the metal internalization step being rate limiting for overall short‐term uptake, intracellular Cd uptake was linear for exposure times less than 20 min at pH 5 or pH 7 for both algal species. After taking into account complexation of Cd in solution, Suwannee River humic substances had no additional effects on cadmium uptake at pH 7, as would be predicted by the free ion model. This absence of effects other than complexation persisted at pH 5, where the tendency of humic substances to adsorb to the algal cell surface is favored. Changes in pH strongly influenced Cd uptake, with the intracellular flux of Cd being at least 20 times lower at pH 5 than at pH 7 for P. subcapitata. Our results support models such as the free ion model or the biotic ligand model, in which humic substances act indirectly on Cd uptake by reducing the bioavailability of Cd by complexation in solution.     

Extraction, isolation and cadmium binding of alginate from Sargassum spp.

Sargassum brown algal species have recently shown promise for use in flow-through column systems that rely on a passive ion-exchange mechanism for the remediation of toxic heavy metals such as Pd, Cd, and Zn from contaminated waters. To elucidate the metal binding mechanism and optimise this so-called biosorption process, detailed information on the biochemistry of the raw biomass and the alginate in particular is essential. This study focuses on the detailed characterisation (e.g., percentage of yield, block co-polymer structure) of the various fractions of material isolated from S. fluitans and S. oligocystum following a (i) standard neutral, (ii) alkaline (NaOH) and (iii) high-temperature alkaline alginate (80 °C; Na₂CO₃) extraction. Results indicate that the alginate yield was independent of the temperature or the extraction method employed (21.1 to 22.8% and 18.9 to 20.5% yields for S. fluitans and S. oligocystum, respectively). Furthermore, ¹H-nuclear magnetic resonance (NMR) analyses revealed that the alginates isolated by the three methods displayed nearly identical doublet -L-guluronic acid frequencies (F _GG; between 0.55 to 0.58 for both S. fluitans and S. oligocystum). Cadmium binding experiments (pH 4.5) further demonstrated that the three alginate extracts have similar metal binding capacities (uptake ranging from 1.59 to 1.81 mmol Cd/gram). The implementation of the high-temperature alkaline extraction procedure resulted in the isolation of a new acid-soluble fraction (ASF), capable of binding cadmium at pH 4.5, which cannot be isolated by the standard neutral extraction protocol. A preliminary characterisation of this ASF revealed the presence of minor quantities of proteins and sulphated polysaccharides, as well as traces of alginate and possibly other low-molecular weight uronic acid-containing polymers.