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Comparison of different sorbents (inorganic and biological) for the removal of Pb 2+ from aqueous solutions
Author(s) -
Suh Jung Ho,
Kim Dong Seog
Publication year - 2000
Publication title -
journal of chemical technology and biotechnology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.64
H-Index - 117
eISSN - 1097-4660
pISSN - 0268-2575
DOI - 10.1002/(sici)1097-4660(200004)75:4<279::aid-jctb217>3.0.co;2-a
Subject(s) - zeolite , activated sludge , chemistry , adsorption , activated carbon , ion exchange , biomass (ecology) , nuclear chemistry , ion exchange resin , aureobasidium pullulans , aqueous solution , biosorption , wastewater , waste management , pulp and paper industry , catalysis , inorganic chemistry , organic chemistry , fermentation , ion , sorption , geology , oceanography , engineering
In an attempt to evaluate the suitability of activated sludge for Pb 2+ removal, a comparative study was carried out using several chemical adsorbents and three types of biomass. The order of Pb 2+ removal capacities for chemical adsorbents was found to be: ion exchange resin > zeolite > granular activated carbon (GAC) > powdered activated carbon (PAC), while for biomass the order was Aureobasidium pullulans  >  Saccharomyces cerevisiae  > activated sludge. Although Pb 2+ removal capacity (mg Pb 2+  g −1 ) of the activated sludge (30.9) was lower than those of the ion exchange resin (167.7) and other pure cultures of A pullulans (170.4) and S cerevisiae (95.3), it was higher than those of other chemical adsorbents such as GAC (26.0), PAC (2.1), and zeolite (30.2). The initial Pb 2+ removal rates for the chemical adsorbents were in the order of PAC > GAC > zeolite > ion exchange resin, while for the biomass samples it was A pullulans  > activated sludge >  S cerevisiae . The initial Pb 2+ removal rate of activated sludge was higher than those of GAC, zeolite, ion exchange resin and S. cerevisiae cells. Therefore, it was concluded that activated sludge that has been used in a municipal wastewater facility can be effectively used in heavy metal removal processes, in situ . © 2000 Society of Chemical Industry

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