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Optimize Flue Gas Settings to Promote Microalgae Growth in Photobioreactors via Computer Simulations

Published: October 1, 2013 doi: 10.3791/50718


Flue gas from power plants is a cheap CO2 source for algal growth. We have built prototype "flue gas to algal cultivation" systems and described how to scale up the algal cultivation process. We have demonstrated the use of a mass-transfer bio-reaction model to simulate and to design the optimal operation of flue gas for the growth of Chlorella sp. in algal photo-bioreactors.


Flue gas from power plants can promote algal cultivation and reduce greenhouse gas emissions1. Microalgae not only capture solar energy more efficiently than plants3, but also synthesize advanced biofuels2-4. Generally, atmospheric CO2 is not a sufficient source for supporting maximal algal growth5. On the other hand, the high concentrations of CO2 in industrial exhaust gases have adverse effects on algal physiology. Consequently, both cultivation conditions (such as nutrients and light) and the control of the flue gas flow into the photo-bioreactors are important to develop an efficient “flue gas to algae” system. Researchers have proposed different photobioreactor configurations4,6 and cultivation strategies7,8 with flue gas. Here, we present a protocol that demonstrates how to use models to predict the microalgal growth in response to flue gas settings. We perform both experimental illustration and model simulations to determine the favorable conditions for algal growth with flue gas. We develop a Monod-based model coupled with mass transfer and light intensity equations to simulate the microalgal growth in a homogenous photo-bioreactor. The model simulation compares algal growth and flue gas consumptions under different flue-gas settings. The model illustrates: 1) how algal growth is influenced by different volumetric mass transfer coefficients of CO2; 2) how we can find optimal CO2 concentration for algal growth via the dynamic optimization approach (DOA); 3) how we can design a rectangular on-off flue gas pulse to promote algal biomass growth and to reduce the usage of flue gas. On the experimental side, we present a protocol for growing Chlorella under the flue gas (generated by natural gas combustion). The experimental results qualitatively validate the model predictions that the high frequency flue gas pulses can significantly improve algal cultivation.


1. Algal Cultivation and Scale-up

  1. Prepare the culture medium using deionized water containing 0.55 g/L-1 urea, 0.1185 g/L-1 KH2PO4, 0.102 g/L-1 MgSO4·7H2O, 0.015 g/L-1 FeSO4·7H2O and 22.5 µl microelements (18.5 g/L-1 H3BO3, 21.0 g/L-1 CuSO4·5H2O, 73.2 g/L-1 MnCl2·4H2O, 13.7 g/L-1 CoSO4·7H2O, 59.5 g/L-1 ZnSO4·5H2O, 3.8 g/L-1 (NH4)6Mo7O24·4H2O, 0.31 g/L-1 NH4VO3). Adjust medium pH to 7-8. Sterilize culture medium via 0.22 µm syringe filter.
  2. Inoculate Chlorella sp. from a single colony on a fresh agar plate into a shake flask containing 50 mL medium with a sterile inoculating loop. Culture algae under 150 rpm and 30 °C for six days (continuous light condition, photon flux = 40-50 µmol m-2 sec-1). Monitor cell density by a spectrophotometer (OD730).
  3. Transfer 50 mL algal culture (middle-log growth phase, OD730 >1) into a 2-L glass flask (with ~1 L sterilized culture medium). Pump filtered air (or CO2) into the culture during the incubation (for 5 days).
  4. Transfer 1 L algal culture into a 20-L glass carboy containing 15 L non-sterilized culture medium (at this stage, risk of microbial contamination is small), then culture algae under same condition as stated in step 1.3.
  5. Place 15 L fresh algal culture (OD730 = 2) and 85 L non-sterilized medium into a flat plate photobioreactor (equipped with light-emitting diodes, computer controller, gas mixture, analyzers for cell optical density, pH, dissolved oxygen, temperature and dissolved CO2). Pump the flue gas/air mixture into the bioreactor.
  6. Thoroughly dry-clean the photobioreactor using 70% ethanol after biomass harvest (OD730 >20).

2. Laboratory Demonstration of Flue Gas Treatment Using Small Photobioreactors

  1. Inoculate algal cultures in glass bottles (200 ml/min medium/bottle, initial OD730 ~0.3).
  2. Burn natural gas and pump the flue gas (~250 cm3 min-1) through a funnel, a condenser tube, and a 0.5 L washing bottle (containing water/limestone slurry).
  3. The mass flow controllers control the flue gas flow into algal culture (Figure 1). Flue gas pulses include two modes: flue gas-on and flue gas-off (pump air instead).

3. Kinetic Model Development

The kinetic model assumes: (1) the cultures are homogeneous systems. (2) CO2 concentration and light intensity in the cultures are the limiting factors for algal growth. (3) CO2 partial pressure and its liquid phase equilibrium with H2CO3, HCO3-, and CO32- is simplified with Henry's Law). The model equations are:

Equations 1 and 2

X is the biomass (kg·m-3). S is the dissolved CO2 (mol·m-3). P is the CO2 partial pressure in the gas phase (Pa). pi is the partial pressure of ith toxic compound in the gas (such as NOx and SOx). Pmax.i is the partial pressure of toxic gas to have full inhibition on biomass growth. ηi is the empirical coefficient. Ks is the Michaelis-Menten constant of CO2 (mol·m-3). KI is the inhibition constant of CO2 (mol·m-3). K is the Michaelis-Menten constant of light intensity (µmol·m-2·sec-1). H is the Henry's constant for CO2 (Pa·m3·mol-1). KLa is the mass transfer rate of CO2 (hr-1). I is the average light intensity, µmol·m-2·sec-1, which can be calculated as follows (Eq. (3)) 9.

Equation 3

The definition of model parameters is in Table 1. The initial conditions assume that biomass and dissolved CO2 concentrations are 100 mg/L and 13 µmol/L, respectively. The volumetric mass transfer coefficient can be estimated by empirical correlation to bioreactor parameters10:

Equation 4

Pg/V is the power consumption of the aerated system in the bioreactor (W/m3). ugs is the superficial velocity of the gas flow through the bioreactor (m/sec). α, β, and γ are constants related to mixing conditions.

  1. Construct a Simulink file for the model simulation (Screen shots are given in the Supporting Material I).
    1. Choose File/New/Model on the MATLAB interface to create a Simulink model, and open "Library Browser" (screen shot 1).
    2. Choose 'Subsystem' block in the library browser to create the Subsystems for Equation 1 and 2. Drag one subsystem block to the Simulink model file, change its name to 'Equation 1', and then repeat the same steps for Equation 2.
    3. Create appropriate blocks and parameters in each subsystem (screen shot 3). Double click the 'Equation 1' block, choose appropriate blocks from the library browser and connect them with arrows that denote the calculation sequence, double click the blocks to set up the parameters, and repeat these steps for the other subsystem.
      Note: 1) The sequence should start with input blocks and conclude with output blocks; 2) The operator blocks for addition, subtraction, multiplication, division and integration can be all found in the library browser, and we suggest users explore the help files of the Simulink to understand how to use them; 3) The optimization solver can be set through the pathway Simulation/Configuration parameters on the toolbar.
    4. Link the two subsystems to represent model equations (1 and 2). Connect the output of one subsystem to the input of the other subsystem by arrow if necessary. For example, the dissolved CO2 concentration is the output in the Equation 2 subsystem, and also the input of the Equation 1 subsystem.
    5. Use 'Pulse Generator' block as the inputs for 'Equation 2' to simulate the on-off CO2 pulses; use 'Constant' block as the surface light input value. Double click the blocks to change the parameters such as the period time and amplitude.
    6. Choose 'Mux' block in the library browser. Connect all the outputs to 'Mux' and then connect it to 'To Workspace' block that stores the simulated results.
    7. Define the 'Simulation stop time' on the top toolbar, click the button "Arrow" to start the simulation, and the results will be shown in the MATLAB workspace (screen shot 4).
  2. Apply dynamic optimization approach to profile optimal CO2 conditions.

To find the changes of inlet inflow CO2 profile (Popt) that maximize biomass production11, MATLAB 'fmincon' function and CVP (control vector parameterization)12 are used. Figure 2 illustrates the optimization algorithm (see MATLAB programming codes in the Supporting Material II).

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Representative Results

Our previous experimental analysis indicates that continuous flue gas exposure adversely affects the Chlorella growth, while decreasing CO2 exposure time is able to alleviate this inhibition13. To better understand the flue gas inflow and algal growth relationship, we develop an empirical model to simulate the biomass growth in the presence of flue gas. We assume that the flue gas contains 15% CO2 (note: The typical CO2 concentration from coal combustion is 10-15%, while flue gas from oxy-combustion power plant has CO2 >15%). The mass transfer and algal growth parameters are based on Table 1. The model simulation tests three methods to avoid growth inhibition by flue gas: 1. Keep low flow rate into the culture to reduce the mass transfer condition. 2. On-off pulses of flue gas into the culture. 3. Control the inflow CO2 compositions at the optimal level.

Firstly, we test the influence of mass transfer rate on the algal growth (Figure 3a), which indicates that optimal mass transfer rate (KLa = 0.17-0.18 hr-1) is able to reduce the flue gas inhibition to algal growth. If KLa is lower or higher than the optimal value, the algal growth will be reduced. Equation 4 suggests the decrease of aeration and gas flow through the culture can reduce the mass transfer coefficient. Table 2 shows how the flow rate (i.e., superficial velocity) affects the algal growth. Generally, low flow rate reduces KLa and prevents CO2 inhibition to algal growth as the same trend shown in Figure 3. Further reducing flow rate through bioreactor will cause the mass transfer coefficient too small to provide enough CO2 for algal growth (Figure 3b).

Secondly, we introduce an on-off flue-gas pulse mode to overcome growth inhibition if flue gas mass transfer KLa is high in the photobioreactor (i.e. KLa = 17 hr-1). In the simulation, we assume the algal cultures are pulsed with two different CO2 concentrations (15% for flue-gas-on and 0.04% with atmospheric CO2 for flue-gas-off). To optimize the flue-gas pulse mode, different on-off frequencies are tested (Figure 4). The simulation shows that high frequency flue gas pulses (on-off control of flue gases) are able to promote algal growth. Table 2 also indicates that on-off control mode uses less flue gas comparing to continuous feeding of flue gas into the bioreactor.

Thirdly, we calculate CO2 concentration profiles for maximal algal growth. Using model parameters in Table 1, the dynamic optimization approach shows the optimal CO2 concentrations in the gas phase should be continuously increased during algal growth. Model simulation also shows that both the on-off CO2 pulses (Method 2) and the control of optimal CO2 input (method 3) are equally good to promote the algal growth with flue gas (Figure 5).

Figure 1
Figure 1. Diagram of the gas on-off control system at laboratory scale. The flow rates of flue gas generated by natural combustion are controlled by the mass flow control system before introduced into the algal system. Click here to view larger image.

Figure 2
Figure 2. Flow chart of dynamic optimization procedures. Click here to view larger image.

Figure 3
Figure 3. Final biomass concentration at day 12 as a function of KLa under continuous flue gas treatment (CO2, 15% v/v) (a), and the comparison of biomass growth with different KLa: 0.017 hr-1 (blue line), 0.17 hr-1 (yellow line), and 17 hr-1 (black line) under continuous flue gas treatment (CO2, 15% v/v) (b). Click here to view larger image.

Figure 4
Figure 4. Effect of gas-on/gas-off frequency on biomass production in 12 days. The model assumes the microalgae are exposed to CO2 (15% v/v) pulses at different tested frequencies. Click here to view larger image.

Figure 5
Figure 5. Comparison of biomass growth under optimal CO2 profile (yellow line), the on-off frequency of 10 sec gas-on/5 min gas-off (red line), on-off control at a frequency of 10 sec gas-on/7 min gas-off (green line), on-off control at a frequency of 1 min gas-on/29 min gas-off (black line), and the continuous treatment with flue gas containing 15% (v/v) CO2 conditions (blue line). Click here to view larger image.

Figure 6
Figure 6. Experimental results from our previous paper13 to show effect of flue gas pulses on Chlorella growth. Gas-on (flue gas treatment); gas-off (air treatment). A: 10 sec gas-on/7 min gas-off; B: 30 min gas-on/30 min gas-off; C: 5 hr gas-on/7 hr gas-off; D: cultivation in shaking flasks. The culture preparation was detailed in the protocol part, and the experiments were conducted under the room temperature. Click here to view larger image.

Parameters Descriptions Values Units References/Notes
µmax maximum specific growth rate 0.070 hr-1 14
kd mortality rate 0.028 hr-1 15
Ks Michaelis-Menten constant of CO2 0.00021 mol·m-3 14
KI inhibition constant of CO2 10 a mol·m-3 16
K Michaelis-Menten constant of light intensity 14 b µmol·m-2·sec-1 9
KLa mass transfer rate of CO2 17 hr-1 17
H henry's constant of CO2 3202 c Pa·m3·mol-1 18
YS/X yield coefficient 100 d (mol CO2)/(kg biomass) 19
A Constant 14.7 m3·kg-1 9
I0 surface light intensity 45 e µmol photons·m-2·sec-1 measured
Atmospheric CO2 atmospheric CO2 concentration 0.04% volume fraction
CO2 in flue gas CO2 concentration in the flue gas 15% volume fraction assumed
X(0) initial biomass concentration 0.1 kg·m- 3 assumed
S(0) initial dissolved CO2 concentration 0.013 mol·m- 3 assumed

Table 1. Parameters used in the model.

KI=10 mM, and the test range in this study is 0.5-10 mol·m-3;
b K=1011 lux, which is ~14 µmol·m-2·sec-1 20;
c H=31.6 atm·M-1;
d 4.4 kg CO2 is needed for production of 1 kg (dry weight) of biomass;
e The measured light intensity is 40-50 µmol·m-2·sec-1;

Superficial velocity /m/s Initial biomass /mg/L γ=0.2 γ=0.5 γ=0.8 Total flue gas used in 12 days (m3/m2)
KLa /m/s Final biomass /mg/L KLa /m/s Final biomass /mg/L KLa /m/s Final biomass /mg/L
0.001* 100 4.3 128 0.54 149 0.068 115 1.0 x 103
0.01* 100 6.8 127 1.7 132 0.43 160 1.0 x 104
0.1* 100 11 126 5.4 127 2.7 129 1.0 x 105
1* 100 17 126 17 126 17 126 1.0 x 106
10* 100 27 126 54 126 107 125 1.0 x 107
10s/5min frequency 100 17 313 17 313 17 313 3.3 x 104

Table 2. Biomass growth with 15% (v/v) flue gas at day 12 under different superficial gas flow velocities. In this model, we assume that KLa=17(ugs)γ

*: Assuming that CO2 is continuously pumped into bioreactor at the constant flow rate.

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In this study, we demonstrate the experimental protocol for scaling up algal cultivations in photobioreactors. We also examine several methods for flue gas inputs to promote algal growth. Using a mass transfer and bio-reaction model, we demonstrate that the CO2 mass transfer coefficient KLa (determined by bioreactor mixing condition and CO2 superficial velocity) strongly influences algal growth. The model simulation indicates continuous on-off flue gas pulses with short pulse width and high on-off frequencies can improve Chlorella growth (i.e. high frequency on-off flue-gas pulses can support biomass growth almost as well as optimal CO2 conditions, Figure 5.). Meanwhile, on-off mode can significantly reduce the total amount of flue-gas that has to be pumped through the bioreactor (Table 2), which saves the energy for transporting the amount of flue gas for algal cultivation. The on-off gas pulse mode can be used in photo-bioreactors or algal ponds, considering that the mode of constant flue gas pulses is much easier to operate than dynamic control of the inflow CO2 concentration. On the other hand, we have performed the algal culture experiments using flue gases. Flue gas are pulsed into the photobioreactors at a specific on/off frequency, which clearly minimizes the inhibitory effect of the flue gas and improves biomass production comparing to cultures using atmospheric CO2 (Figure 6)13. The experimental results have qualitatively verified our model and confirmed that the on-off control of the flue gas is effective for increasing Chlorella growth.

Finally, this model study is subject to several limitations. First, the model does not directly consider the effects from toxic compounds such as the SOx and NOx in the flue gas. Second, the chemical reactions and equilibriums in the culture medium (include CO2, H+, OH-, NH3, etc.) are simplified. Third, the model does not take into account CO2 fluid dynamics, where the actual gaseous mass transfer is not instantaneous or homogeneous in culture medium. However, the simplified model approaches still have practical applications for providing guidelines for optimizing algal growth.

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These authors have nothing to disclose.


This study is supported by an NSF program (Research Experiences for Undergraduates) at Washington University in St. Louis.


Name Company Catalog Number Comments
Spectrophotometer Thermal Scientific, Texas USA
CO2 gas analyzer LI-COR, Biosciences, Nebraska USA
Mass flow controllers OMEGA Engineering INC, Connecticut USA FMA5416
Data acquisition card Measurement Computing Corporation, Massachusetts USA USB-1208FS
Filters Aerocolloid LLC, Minnesota USA
MATLAB/Simulink Mathworks, Massachusetts USA R2010a
Glass bottles Fisher USA



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Optimize Flue Gas Settings to Promote Microalgae Growth in Photobioreactors via Computer Simulations
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Cite this Article

He, L., Chen, A. B., Yu, Y., Kucera, More

He, L., Chen, A. B., Yu, Y., Kucera, L., Tang, Y. Optimize Flue Gas Settings to Promote Microalgae Growth in Photobioreactors via Computer Simulations. J. Vis. Exp. (80), e50718, doi:10.3791/50718 (2013).

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