CARBON OXIDATION - NITRMCATION IN ATTACHED GROWTH ACTIVATED SLUDGE REACTORS
CARBON OXIDATION - MTRMCATION IN ATTACHED GROWTH ACTIVATED SLUDGE REACTORS K. Baskaran and C. Polprasert Environmental Engineering Division, Asian Ins...
CARBON OXIDATION - MTRMCATION IN ATTACHED GROWTH ACTIVATED SLUDGE REACTORS K. Baskaran and C. Polprasert Environmental Engineering Division, Asian Institute ofTechnology, GP.O. Box 2754, Bangkok 10501, Thailand
ABSTRACT
Experiments on attached-growth activated sludge (AGAS) were conducted to investigate the AGAS efficiency in carbon oxidation-nitrification. Laboratoryscale AGAS reactors were installed with ring lace media to serve as support for the growth of attached-growth microorganisms. It was found that the AGAS reactor with 10% media volume gave the maximum biomass (both dispersed and attached growth) in the reactor. The AGAS reactors were more effective in the carbon oxidation-nitrification than the control reactor without attachedgrowth media. There was less sludge production in the AGAS reactors which should result in lower cost in waste sludge treatment and disposal. A Monoddiffusion model proposed in this study was found to be satisfactory in describing COD removal in the AGAS reactors. KEYWORDS Activated sludge; attached growth; carbon oxidation; nitrification; kinetics. INTRODUCTION In recent years, much efforts have been made to improve the effluent quality by utilizing both dispersed and attached growth microorganisms. The Activated sludge process in which an aeration tank is incorporated with an attached growth media is called attached growth activated sludge (AGAS) process. It was reported in the literature that the AGAS processes were capable of achieving high percentages of carbon oxidation as well as nitrification, while maintaining operational stability. However« information regarding the kinetics and the process efficiency of the combined system on carbon oxidation and nitrification are not presently available. Thus, the process constraints, the mathematical model to predict the effluent quality, and the process design, are not properly investigated. This study was conducted with the following objectives: - to investigate the process efficiency of the AGAS in the removal of carbonaceous and nitrogenous compounds; - to determine the kinetic parameters of the AGAS process; - to investigate the nitrification efficiency of AGAS; and - to develop a mathematical model to predict the effluent chemical oxygen demand (COD) concentrations of the AGAS reactors.
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MATHEMATICAL MODEL FOR CARBON OXIDATION IN AGAS REACTORS In an AGAS reactor, the combined carbon oxidation-nitrification will be carried out by both suspended and attached growth microorganisms, causing development of mathematical models rather complicated. For simplification, a conceptual model of AGAS is proposed as shown in Fig.l.
Sis
Ses Effluent
Influent Dispersed growth portion Fig.l.
Attached growth portion
Conceptual model of AGAS
where, S o s = influent substrate concentration, mg/L s is s substrate concentration after dispersed growth portion, mg/L S e s = effluent substrate concentration, mg/L According to Fig. 1, the carbon oxidation- nitrification were assumed to occur firstly in the dispersed growth portion and secondly in the attached growth portion.The Monod expression was used to describe the dispersed growth reactions, whereas a diffusion model was used to simulate the attached growth reactions. In a continuous flow reactor, substrate is the rate limiting factor. Using Monod and mass balance equations, the effluent concentration of a dispersed growth reactor is given by: ( 1 + kdec )
(1)
öc ( Um - kd > = * =
where, Ks *d
ec
half velocity constant, mg/L endogenous decay coefficient, day"* solid retention time, days maximum specific growth rate, day"*
Um In the attached growth portion, the biofilm depth was assumed to be limited only by the nutrient availability, whereas substrate uptake rate was limited by carbon concentration. The carbon oxidation within the biofilm was assumed to follow Monod kinetics. The surface flux of carbon into a deep biofilm can be calculated as given below (STRAND, 1986): u
F = [2D ( cf c where, Fcf Dc Uc Xc Yc To kd is of
■ ■ = = *
c xc
)]°-5[S - K Log (1 + is c e
Si s
)] 0 · 5
(2)
surface flux of COD, mg COD/(m2-dav) diffusivity of COD in biofilm, cm*-day"*1 effective maximum specific growth rate of heterotrophs, day -1 heterotrophic biomass concentration in biofilm, mg VSS/mL effective heterotrophic COD yield, mg VSS/mg COD
estimate the carbon removal by the biofilm, the values of D c = 0.29 m2/day; = K C - 0.05 day -1 ; Y c = 0.0269 mg VSS/mg COD [STRAND, 1986] were used.If A the total surface area (cm2) of the attached growth media, then the amount COD penetrated (uptaken) into the biofilm is given by:
Carbon Oxidation - Nitrification s
COD = A ' Fcf where, ScoD = C0D removed by the biofilm, mg COD/day If Q is the flowrate (in L/day), then: S COD therefore, S