BIOSORPTION OF HIGH-MOLECULAR-WEIGHT ORGANOCHLORINES IN PULP-MILL EFFLUENT

Authors
Citation
G. Yan et Dg. Allen, BIOSORPTION OF HIGH-MOLECULAR-WEIGHT ORGANOCHLORINES IN PULP-MILL EFFLUENT, Water research, 28(9), 1994, pp. 1933-1941
Citations number
35
Categorie Soggetti
Engineering, Civil","Environmental Sciences","Water Resources
Journal title
ISSN journal
00431354
Volume
28
Issue
9
Year of publication
1994
Pages
1933 - 1941
Database
ISI
SICI code
0043-1354(1994)28:9<1933:BOHOIP>2.0.ZU;2-6
Abstract
Since biosorption is considered an important step in the removal of or ganochlorines in secondary treatment systems from pulp and paper mill effluent, the role of biosorption in the removal of high molecular wei ght organochlorine (HMW AOX) was studied. UItrafiltered (> 1000 Da) to tal mill effluent was used as the sorbate and municipal sewage sludge as the sorbent. Eight different parameters were tested: contact time, cell viability, cell concentration, sorbate concentration, desorption, cell type, sorbate type and temperature. Biosorption equilibrium was reached in the first 30 min of an experiment and the removal of the hi gh molecular weight organochlorine was independent of cell viability. The biosorption was characterized by the Freundlich isotherm [Q(mg/g V SS) = KC1/n, C = AOX concentration (mg/l)]; the observed values for th e Freundlich coefficients K and 1/n were 1.83 and 0.53, respectively. The Langmuir isotherm [Q = 7.5 C/(3.2 + C)] provided a better characte rization for biosorption of HMW AOX since it predicted a saturation bi omass phase concentration of 7.5 mg Cl/g VSS at high AOX concentration s. The maximum percentage removal of HMW AOX was 70% at a biomass conc entration of 2.0 g VSS/1 or higher. About 8% of the organochlorines de sorbed from live biomass after 24 h indicating that the process is not readily reversible. Based on the experiments at various temperatures, the enthalpy of sorption was found to be -4 kJ/mol Cl.