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      Enhanced Lead Sorption by Biochar Derived from Anaerobically Digested Sugarcane Bagasse

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      Separation Science and Technology
      Informa UK Limited

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          Biosorbents for heavy metals removal and their future.

          A vast array of biological materials, especially bacteria, algae, yeasts and fungi have received increasing attention for heavy metal removal and recovery due to their good performance, low cost and large available quantities. The biosorbent, unlike mono functional ion exchange resins, contains variety of functional sites including carboxyl, imidazole, sulphydryl, amino, phosphate, sulfate, thioether, phenol, carbonyl, amide and hydroxyl moieties. Biosorbents are cheaper, more effective alternatives for the removal of metallic elements, especially heavy metals from aqueous solution. In this paper, based on the literatures and our research results, the biosorbents widely used for heavy metal removal were reviewed, mainly focusing on their cellular structure, biosorption performance, their pretreatment, modification, regeneration/reuse, modeling of biosorption (isotherm and kinetic models), the development of novel biosorbents, their evaluation, potential application and future. The pretreatment and modification of biosorbents aiming to improve their sorption capacity was introduced and evaluated. Molecular biotechnology is a potent tool to elucidate the mechanisms at molecular level, and to construct engineered organisms with higher biosorption capacity and selectivity for the objective metal ions. The potential application of biosorption and biosorbents was discussed. Although the biosorption application is facing the great challenge, there are two trends for the development of the biosorption process for metal removal. One trend is to use hybrid technology for pollutants removal, especially using living cells. Another trend is to develop the commercial biosorbents using immobilization technology, and to improve the biosorption process including regeneration/reuse, making the biosorbents just like a kind of ion exchange resin, as well as to exploit the market with great endeavor.
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            Agricultural waste material as potential adsorbent for sequestering heavy metal ions from aqueous solutions - a review.

            Heavy metal remediation of aqueous streams is of special concern due to recalcitrant and persistency of heavy metals in environment. Conventional treatment technologies for the removal of these toxic heavy metals are not economical and further generate huge quantity of toxic chemical sludge. Biosorption is emerging as a potential alternative to the existing conventional technologies for the removal and/or recovery of metal ions from aqueous solutions. The major advantages of biosorption over conventional treatment methods include: low cost, high efficiency, minimization of chemical or biological sludge, regeneration of biosorbents and possibility of metal recovery. Cellulosic agricultural waste materials are an abundant source for significant metal biosorption. The functional groups present in agricultural waste biomass viz. acetamido, alcoholic, carbonyl, phenolic, amido, amino, sulphydryl groups etc. have affinity for heavy metal ions to form metal complexes or chelates. The mechanism of biosorption process includes chemisorption, complexation, adsorption on surface, diffusion through pores and ion exchange etc. The purpose of this review article is to provide the scattered available information on various aspects of utilization of the agricultural waste materials for heavy metal removal. Agricultural waste material being highly efficient, low cost and renewable source of biomass can be exploited for heavy metal remediation. Further these biosorbents can be modified for better efficiency and multiple reuses to enhance their applicability at industrial scale.
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              Sorption of arsenic, cadmium, and lead by chars produced from fast pyrolysis of wood and bark during bio-oil production.

              Bio-char by-products from fast wood/bark pyrolyses, were investigated as adsorbents for the removal of the toxic metals (As(3+), Cd(2+), Pb(2+)) from water. Oak bark, pine bark, oak wood, and pine wood chars were obtained from fast pyrolysis at 400 and 450 degrees C in an auger-fed reactor and characterized. A commercial activated carbon was also investigated for comparison. Chars were sieved (>600, 600-250, 250-177, 177-149, and <149 microm) and the particle size fraction from 600 to 250 microm was used without further modification for all studies unless otherwise stated. Sorption studies were performed at different temperatures, pHs, and solid to liquid ratios in the batch mode. Maximum adsorption occurred over a pH range 3-4 for arsenic and 4-5 for lead and cadmium. Kinetic studies yielded an optimum equilibrium time of 24 h with an adsorbent dose of 10 g/L and concentration approximately 100 mg/L for lead and cadmium. Sorption isotherms studies were conducted in broad concentration ranges (1-1000 ppb for arsenic, 1x10(-5)-5x10(-3) M for lead and cadmium). Oak bark out-performed the other chars and nearly mimicked Calgon F-400 adsorption for lead and cadmium. In an aqueous lead solution with initial concentration of 4.8x10(-4) M, both oak bark and Calgon F-400 (10 g/L) removed nearly 100% of the heavy metal. Oak bark (10 g/L) also removed about 70% of arsenic and 50% of cadmium from aqueous solutions. Varying temperatures (e.g., 5, 25, and 40 degrees C) were used to determine the effect of temperatures. The equilibrium data were modeled with the help of Langmuir and Freundlich equations. Overall, the data are well fitted with both the models, with a slight advantage for Langmuir model. The oak bark char's ability to remove Pb(II) and Cd(II) is remarkable when considered in terms of the amount of metal adsorbed per unit surface area (0.5157 mg/m(2) for Pb(II) and 0.213 mg/m(2) for Cd(II) versus that of commercial activated carbon.
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                Author and article information

                Journal
                Separation Science and Technology
                Separation Science and Technology
                Informa UK Limited
                0149-6395
                1520-5754
                July 15 2011
                July 15 2011
                : 46
                : 12
                : 1950-1956
                Article
                10.1080/01496395.2011.584604
                bc160240-34c1-49b0-892a-c2a137da1833
                © 2011
                History

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