2013
DOI: 10.1080/10889868.2013.827622
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Biodegradation Kinetic Studies on Phenol in Internal Draft Tube (Inverse Fluidized Bed) Biofilm Reactor UsingPseudomonas fluorescens: Performance Evaluation of Biofilm and Biomass Characteristics

Abstract: The bioremediation potential of Pseudomonas fluorescens was studied in an internal draft tube (inverse fluidized bed) biofilm reactor (IDTBR) under batch recirculation conditions using synthetic phenol of various concentrations (400, 600, 800, 1000, and 1200 mg/L). The performance of IDTBR was investigated and the characteristics of biomass and biofilm were determined by evaluating biofilm dry density and thickness, bioparticle density, suspended and attached biomass concentration, chemical oxygen demand, and … Show more

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Cited by 18 publications
(4 citation statements)
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“…as for toxic substrates, rates at higher concentrations of substrates are often inhibitory and under this conditions, other substrate inhibition model such as Haldane, Teissier-Edwards, Yano, Aiba and Luong are more often observed [15,16,29,42]. The Monod model is observed for toxic substrate under mostly specific conditions, where the microorganisms are being immobilized in the forms of artificial substrate like gellan gum or polyacrylamide or biofilm [43][44][45][46][47][48][49][50][51].…”
Section: Resultsmentioning
confidence: 99%
“…as for toxic substrates, rates at higher concentrations of substrates are often inhibitory and under this conditions, other substrate inhibition model such as Haldane, Teissier-Edwards, Yano, Aiba and Luong are more often observed [15,16,29,42]. The Monod model is observed for toxic substrate under mostly specific conditions, where the microorganisms are being immobilized in the forms of artificial substrate like gellan gum or polyacrylamide or biofilm [43][44][45][46][47][48][49][50][51].…”
Section: Resultsmentioning
confidence: 99%
“…The preliminary stage of upstream processing work started with reviving the host by subsequent streaking of a mother culture of P.fluorescens on a Pseudomonas agar slant and keeping it for incubation at 28°C for 2 days. Primary culture was prepared by transferring two loops of microorganisms having concentration of 4.1 × 10 4 colonies/mL from the agar slant into 100 mL of feed medium containing 20 mL of mineral salt medium and 80 mL of phenol from the initial substrate (phenol) concentration of 1200 mg/L in four 250 mL conical flasks . They were kept in a shaker incubator at a temperature of 28°C and agitated at a speed of 120 rpm.…”
Section: Methodsmentioning
confidence: 99%
“…Primary culture was prepared by transferring microorganisms into feed medium containing mineral salt medium [20] and pharmaceutical biomedical wastewater which were then kept in incubator to attain steady state growth. Secondary culture was then developed from primary and was used as inoculum for the formation of biofilm onto polystyrene support particles in IFFBR [21].…”
Section: Microorganismmentioning
confidence: 99%