Bioreactors: BY Agomuoh Paul Kelechi 20111200 Cyprus International University DEC 27, 2011
Bioreactors: BY Agomuoh Paul Kelechi 20111200 Cyprus International University DEC 27, 2011
Bioreactors: BY Agomuoh Paul Kelechi 20111200 Cyprus International University DEC 27, 2011
TABLE OF CONTENTS
1. INTRODUCTION TO BIOREACTORS AND THEIR ROLE IN BIOTECHNOLOGY. 2. CLASSIFICATION AND TYPES OF BIOREACTORS 3. REACTORS ARRANGEMENTS
A bioreactor is a vessel in which a chemical process is carried out which involves organisms or biochemically active substances derived from such organisms. This process can either be aerobic or anaerobic
The Role of bioreactors in biotechnology: To reach its necessary goals, the biotechnological process has usually 3 major stages: 1. Preparation of nutrient media for the cultivated microorganism and the cultivation process; 2.The course of the microorganism reproduction process in bioreactors (called also fermenters) or in other equipment; 3. Obtaining of the final product or substance from the cultivated medium. This stage includes operations such as separation, purification and other technologies, which are connected with obtaining the commodity form.
2. BIOFILM BIOREACTORS: In biofilm reactors most of the microorganisms are attached to a surface, and in this manner kept within the reactor. Biofilm is also used regularly for wastewater treatment, and the bacteria can either absorb or break down toxic substances in the water. The different kinds of biofilm reactors include membrane, fluidized bed, packed bed, airlift, and upflow anaerobic sludge blanket reactors.
THE BATCH BIOREACTOR: A typical batch reactor consists of a tank with an agitator and integral heating/cooling system. These vessels may vary in size from less than 1 litre to more than 15,000 litres. They are usually fabricated in steel, stainless steel, glass lined steel, glass or exotic alloy
Liquids and solids are usually charged via connections in the top cover of the reactor. Vapors and gases also discharge through connections in the top. Liquids are usually discharged out of the bottom.
ADVANTAGES OF THE BATCH BIOREACTOR 1. EASY OPERATION AND ABSENS EOF MECHANICAL PUMPS 2. VERSATILITY; A SINGLE VESSEL CAN CARRY OUT A SEQUENCE OF DIFFERENT OPERATIONS DISADVANTAGES 1. WHERE MIXING IS A CRITICAL PARAMETER , THEY ARE NOT THE IDEAL SOLUTION
This is also referred to as a tubular reactor or a piston- flow reactor. The liquid or slurry stream continuously enters one end of the reactor and leaves at the other end. In the ideal plug flow reactor (PFR) we envision that flow moves through the reactor with no mixing with earlier or later entering flows. The concentration of substrates and microorganisms vary throughout the reactor. Concentrations of substrates are highest at the entrance of the reactor, which tends to make rates there quite high ADVANTAGES: 1. Can run for long periods of time without maintenance. 2. The heat transfer rate can be optimized by using more, thinner tubes or fewer, thicker tubes in parallel.
DISADVANTAGES: 1. Temperatures are hard to control and can result in undesirable temperature gradients
2. Expensive to maintain.
BIOFILM REACTORS
The medium to which the microorganisms are attached is stationary (e.g plastic media or pea sized stones). Commonly packed bed reactors are used for aerobic treatment of waste waters and are known as tricking filters and or biological towers.
ADVANTAGES:
1. There is improved contact between the waste stream and the micro organisms .
ADVANTAGES: 1. Uniform particle mixing 2.Uniform temperature gradients 3. The ability to operate reactor in conitnuos state.
DISADVANTAGE: 1. Increased reactor vessel size 2. pumping requirements and pressure drop 3. Pressure loss scenario
REACTOR ARRANGEMENTS
RECYCLE OF SETTLED SOLIDS
REACTORS IN SERIES
REACTORS IN PARALLEL
MASS BALANCES
A mass balance (also called a material balance) is an application of conservation of mass to the analysis of physical systems. By accounting for material entering and leaving a system, mass flows can be identified which might have been unknown, or difficult to measure without this technique.
The mass balance is the key to design and analysis of microbial processes. A mass balance is provided by a balanced stoichiometric chemical equation. EXAMPLE: 0.0333C6H5COO- + 0.12NO3- + 0.002NH4+ + 0.12H+ -----0.02 C5H7O2N + 0.06N2 +0.12CO2 +0.0133HCO3 + 0.1067H2O 0.033C6H5COO- = BENZOATE TO BE CONSUMED BY MICROBES 0.12NO3- = ELECTRON ACCEPTOR 0.02NH4+ = AMMONIUM TO BE CONSUMED BY MICROBES AS NUTRIENT 0.O2C5H702N = BIOMASS PRODUCED AFTER DEGRADATION BY MICROBES 0.06N2, 0.12C02, 0.0133HCO3, 0.1067H2O =(NIRTROGEN,CARBON DIOXIDE , CARBONATE AND WATER PRODUCED DUE TO THE DEGRADATION
A very important aspect of mass balances is that each component must have their own mass balance. Components may include, oxygen, electron acceptor, TOC, COD,biomass, ammonium and nitrate and macro nutrients.
RATE OF MASS ACCUMULATION = IN CONTROL VOLUME RATE(S) MASS IN RATE(S) OF MASS OUT + RATE OF MASS GENERATION
Where d(VC)/dt = Rate of mass accumulation in control volume Q in = flow rate into the system Q out = flow rate out of the system C = Concentration of stream/substrate R = Rate of reaction V = Volume of the stream/ substrate The inflow and outflow stream rates are zero, Q in Q out = 0 Hence , we have d(VC)/dt = R.V ( if reactant volume changes significantly) or d(C)/dt = R ( if reactant volume remains constant) R= k. C, where k = rate constant, c = concentration
Writing the material balance for this reactor gives, d(VC)/dt = Q in.Cin - Q out.Cout + R.V If the reactor volume is constant and the volumetric flow rates of the inflow and outflow streams are the same, then d(C)/dt = 1/ ( C in - C out + R) This parameter = V/Q in it is called the mean residence time of the CSTR. We refer to this balance as the constant-density case. It is often a good approximation for liquid-phase reactions. for steady state: The steady state of the CSTR is described by setting the time derivative in the expression d(VC)/dt = 0 0 = Q in . C in - Q out . C out + R.V Conversion of reactant x is defined for a steady-state CSTR as follows: X = ( Q in. C in - Q out. C out) / Q in .C in
PICTORALS
CONCLUSIONS
Bioconversion of wastes to harmless substances or higher value products already has a significant role in environmental pollution control and improved resource utilization. Both insitu and bioreactor based treatment processes are experiencing rapid development and increasing deployment in practical applications.