CO₂-Derived Carbon Capture Using Microalgae and Sodium Bicarbonate in a PhotoBioCREC Unit: Kinetic Modeling

Abstract

By converting bicarbonates via Chlorella vulgaris photosynthesis, one can obtain valuable biofuel products and find a route toward carbon-derived fossil fuel conversion into renewable carbon. In this research, experiments were carried out in the PhotoBioCREC prototype under controlled radiation and high mixing conditions. Sodium bicarbonate (NaHCO₃) was supplied as the inorganic carbon-containing species, at different concentrations, in the 18 to 60 mM range. Both the NaHCO₃ concentrations and the organic carbon concentrations were quantified periodically during microalgae culture, with the pH being readjusted every day to the 7.00 level. It was found that sodium bicarbonate was converted with a selectivity up to 33.0% ± 2.0 by Chlorella vulgaris. It was also observed that the reaction rate constant for inorganic carbon conversion was 0.26 ± 0.09 ${\mathrm{day}}^{-1}$, while the maximum reaction rate constant for organic carbon formation was achieved with a 28 mM NaHCO₃ concentration and displayed a 1.18 ± 0.05 ${\mathrm{mmole}\mathrm{L}}^{-1}{\mathrm{day}}^{-1}$ value.

1. Introduction

Innovative processes are required to reduce the use of fossil fuels and promote the consumption of anthropogenic carbon dioxide (CO₂). It is broadly acknowledged that terrestrial plants can only capture a fraction of the CO₂ produced in electricity power plants and transportation vehicles, via photosynthesis. Some microorganisms, such as microalgae, can perform enhanced photosynthesis in specially designed reactors [1], contributing very effectively to CO₂ capture [2]. The produced microalgae frequently designated as biomass is an attractive feedstock for biofuel and/or energy production in carbon-neutral processes [3,4].

The culturing of microalgae in either an open pond or a closed photobioreactor requires the supply of inorganic carbon. This can be done by using gaseous CO₂ directly from a combustion process or alternatively by using soluble carbonates (i.e., bicarbonates). The latter option has the advantage of providing carbon-containing species of high solubility in water (i.e., 9.6 g of NaHCO₃/100 g of water versus 0.1688 g of CO₂/100 g of water, at 20 °C and atmospheric pressure [5]), while allowing carbon to be incorporated in the microalgae cell structure as organic carbon [6,7]. Thus, as the growth rates of microalgae are influenced by the availability of dissolved inorganic carbon species in the medium [8], the use of soluble carbonates species can result in a much higher carbon fixation efficiency [2]. Furthermore, one should note that there may be other factors affecting microalgae growth, including: (a) nutrients (i.e., nitrogen and phosphorous), (b) visible light, (c) mixing, (d) pH, and (e) temperature [9]. Therefore, all these microalgae growth parameters must be carefully controlled to achieve maximum efficiency in the carbon conversion into microalgae.

Despite the claimed advantages of carbon capture using microalgae, there are still important issues to be addressed, related to the scaling up of this process, such as the culture microalgae growth rate [10]. The lack of this information limits the commercialization of the microalgae growth technology [10]. To overcome this, the optimization of microalgae growth has to be accomplished through a better understanding of the interaction between reaction rate, visible light radiation, and absorption and media hydrodynamics [11].

Regarding kinetic models for microalgae growth published in the technical literature, the Monod model is widely used to predict the specific microorganism growth rate, under light saturation conditions [12,13,14,15]. Later, in other studies, growth rate modifications have been reported, including growth inhibition, due to both the lack of nutrients or nutrient concentrations that are too high [16,17,18]. Kumar and Das [19] and Chang et al. [20] used the logistic equation (Equation (1)), as first proposed by Verhulst (1844) and Pear and Reed (1920), to explain the different phases of the microalgae growth (lag, exponential, and stationary) with this rate being postulated as independent of the substrate concentration [17,19,20]:

$$\frac{dX}{dt}=K_{C}X\left(1-\frac{X}{X_{max}}\right)$$

(1)

where X represents the dry cell weight (g L⁻¹), $X_{max}$ is the maximum dry cell weight (g L⁻¹), and $K_C$ stands for the apparent specific growth rate of the microalgae (day⁻¹).

Regarding the microalgae growth rate, few studies have determined algae growth kinetic parameters, including the effect from inorganic carbon concentration from bicarbonate solutions. The focus has been on the use of gaseous CO₂ [13,21].

Table A1. Microalgae kinetic models reported in the technical literature.

Authors	Conditions of Runs		Quantum Yield Evaluation	Kinetics
	Mixing Evaluation	Radiation Absorption Evaluation		TOC/Biomass	Substrate (CO2 or NaHCO3)
Novak and Brune [22]	?	no	No	First order and Monod	none
de Morais and Costa [12]	No(intermittent aeration with air-CO2)	No	No	First order	None
Jacob-Lopes et al. [13]	No(bubble column PBR)	No	No	First order	First order
Yeh et al. [23]	Yes	No	No	First order and Monod model	None
Chun-Yen et al. [34]	Yes	No	No	First order and Monod model	None
Kumar and Das [19]	Yes	No	No	First order and logistic equation	None
Lam and Lee [14]	Yes	No	No	First order	None
Chang et al. [20]	?	No	No	First order, Logistic equation	None
Adamczyk et al. [2]	?	No	No	Logistic equation	None
This study	Yes	Yes	Yes	Zero order	First order

Notes: (a) the “yes” corresponds to a quantitative evaluation of either “cell unit mixing” or “the cell unit radiation absorption” during runs; (b) the “No” corresponds to the lack of provided data about “mixing” or “radiation absorption”; (c) the “?” symbol corresponds to cases where there is uncertainty regarding “the mixing conditions” or “the radiation absorption”; and (d) the “zero order,” “first order,” or “the Monod model” corresponds to observed kinetics during experiments.

reports a summary of the kinetic models available in the technical literature [2,12,13,14,19,20,22,23], highlighting the main issues considered: (a) the effect of mixing and radiation absorption, (b) the quantum yield evaluation, (c) the kinetic model development with the simultaneous measurement of total organic carbon (TOC) formed, and (d) the inorganic carbon substrate consumed.

One can notice in Table A1 that even if these proposed kinetics can be considered valuable as first approximations, they still lack the following: (a) the development of macroscopic irradiation energy balances, (b) the assessment of carbon balances, (c) a critical review of kinetic model assumptions applicability, and (d) the determination of kinetic parameters using statistical indicators.

Given the above, the present study focused on rigorously establishing phenomenologically based growth kinetics for CPCC90 Chlorella vulgaris. The selectivity reported for Chlorella vulgaris and the resulting kinetic model are original and have not been previously reported. These growth kinetics were established for a wide range of bicarbonate concentrations. They adequately predicted both bicarbonate and organic carbon concentrations at various culture times, while effectively determining the efficiency of inorganic carbon conversion into microalgae biomass.

2. Materials and Methods

2.1. Microalgae Strain and Medium

The green algae CPCC90 Chlorella vulgaris obtained from the Canadian Phycological Culture Centre (CPCC) of the University of Waterloo, Canada was used throughout the experiments. A modified Bold Basal Medium (BBM) was employed to grow the microalgae with different concentrations of sodium bicarbonate (NaHCO₃). As reported previously [1], the medium purchased from CPCC was sterile and ready to be used. The composition of the medium was (g/L): 0.175 KH₂PO₄, 0.025 CaCl₂·2H₂O, 0.075 MgSO₄·7H₂O, 0.25 NaNO_3, 0.075 K₂HPO₄, 0.025 NaCl, 0.01 Na₂EDTA·2H₂O, 0.0062 KOH, 0.00498 FeSO₄·7H₂O, and 0.00805 H₃BO₃, and contained a trace metal solution with 2.86 g/L of H₃BO₃, 1.81 g/L of MnCl₂·4H₂O, 0.222 g/L of ZnSO₄·7H₂O, 0.390 g/L of Na₂MoO₄·2H₂O, 0.079 g/L of CuSO₄·5H₂O, and 0.0494 g/L of Co(NO₃)₂·6H₂O.

2.2. Experimental Setup

A detailed explanation of the PhotoBioCREC prototype used in this research was already reported previously by us [1]. The PhotoBioCREC of the present study was specifically designed to carry out the experiments using the CPCC90 Chlorella vulgaris at the Chemical Reactor Engineering Center (CREC) at the University of Western Ontario. The PhotoBioCREC has a semiconical shape in the lower section, which promotes a vortex flow and prevents the formation of dead zones. Moreover, it has vertical baffles that complement the mixing provided by a cross-magnetic stirrer, placed in the bottom section of the photobioreactor. The described vertical baffles increase both the mixing and turbulence. Photos of the PhotoBioCREC prototype with microalgae CPCC90 Chlorella vulgaris are presented in Figure 1.

To determine the kinetic parameters of carbon fixation, experiments with CPCC90 Chlorella vulgaris, grown in BBM with four different nominal concentrations of NaHCO₃, were developed in a 175 mL volume solution capacity unit. The nominal concentrations of NaHCO₃ tested were 18, 28, 40, and 60 mM. Three repeats for each experimental run were effected for each concentration studied. Thus, all reported concentrations in the present article are average values, with their respective reported standard deviations.

Furthermore, the pH of the culture was monitored and re-adjusted to the value of 7.00, every 24 h, by employing both hydrochloric acid (HCl) at a 1.0 mol/L concentration and sodium hydroxide (NaOH) at a 1.0 mol/L concentration, as required. A cool white fluorescent lamp provided the radiation energy required by the culture for a period of 12 h. This was followed by a dark cycle of 12 h. This was performed to simulate the eventual expected cycles of visible light (day and night) that could be used to irradiate the culture in equatorial-region countries, such as Costa Rica. The temperature in the photobioreactor was 24.6 ± 0.8 °C. A magnetic stirrer was used to provide mixing at 700 rpm [1]. The quantification of organic and inorganic carbon, pH, and transmitted irradiation was performed daily. In addition, during operation, suspended 1–2 mm diameter alumina particles were added to the culture system to keep the reactor walls clean and without microalgae deposition. It was found that 0.3 g of alumina particles in a 175 mL microalgae culture (0.05% volume concentration) was adequate to achieve this objective, with only a 5% reduction in the prototype-transmitted visible light [1].

2.3. Analytical Methods

The analytical methods used in the present study were reported in a previous publication of our research team [1]. Samples were taken every 24 h, to monitor the culture growth, by quantifying the total organic carbon (TOC) produced, using a TOC-Shimadzu analyzer V_CPH. Using this approach, it was considered that the approximate amount of carbon involved in the culture growth, due to the soluble microbial products, was negligible, in comparison with all other organic species contained in the cells. This is in agreement with results reported by Babaei and Mehrnia [24]. Prior to the TOC analysis, samples were pretreated with 2.0 mol/L of HCl and sparged with nitrogen for 10 min, to eliminate the inorganic carbon present. Moreover, the inorganic carbon concentration at various culture times was determined via titration with a Digital pH meter Thermo Scientific Orion Star (Canada). The titration endpoint was determined using a pH derivative plot [25].

2.4. Inorganic Carbon Conversion Efficiency

The efficiency in the utilization of inorganic carbon by the CPCC90 Chlorella vulgaris can be reported as carbon conversion. This efficiency can be expressed as the ratio of the moles of organic carbon produced over the initial moles of inorganic carbon:

$$\eta =\frac{molesoforganiccarbonproduced}{molesofinitialinorganiccarbon}*100$$

(2)

2.5. Microalgae Characterization

The characterization of microalgae was obtained through the analysis of the cells, by quantifying their components using combined elemental analyzer/isotope ratio mass spectrometry and energy-dispersive X-ray spectroscopy (EDX). Microalgae CPCC60 Chlorella vulgaris cell sizes were analyzed using the microscope Z1 Imager by Zeiss.

The image analysis was complemented with a scanning electron microscope (SEM) analysis. This involved treating samples with 1% glutaraldehyde (in BBM) for 2.5 days at 4 °C. The resulting cells were washed with a BBM buffer. Biomass was treated with osmium vapor for 1 h. After that, filtered biomass was rinsed with water to eliminate the osmium and then dehydrated with ethanol at different concentrations (30% to 100%). The ethanol-dehydrated samples were dried using a Critical Point Dryer followed by the needed coating for the SEM analysis [26].

Furthermore, algal biomass was recovered by centrifugation in order to quantify carbon, hydrogen, nitrogen, and sulfur atomic weight fractions. Three centrifugation cycles were performed to concentrate the biomass, which was then washed with distilled water to remove any nutrients [27]. Following centrifugation and washing, the biomass was freeze-dried to retain an unaltered sample before proceeding to analysis quantification.

3. Modeling Algae Growth

As mentioned previously, inorganic carbon species can be fed to the PhotoBioCREC unit, as bicarbonates. These species can be converted, in principle, into organic carbon as microalgal biomass, CO₂, sodium carbonate, and sodium hydroxide. As a result, an overall bicarbonate conversion stoichiometry can be considered as follows:

$$2NaHC{O}_3\to \alpha C{H}_a{O}_b\left(biomass\right)+\beta C{O}_2+\omega N{a}_{2}C{O}_3+\phi NaOH+\upsilon H_{2}O$$

(3)

where $\alpha , \beta , \omega , \phi$, and υ are, respectively, the stochiometric coefficients for organic carbon as biomass, for CO₂, for sodium carbonate, for sodium hydroxide, and for water (see Appendix B and Appendix C for details of parameters’ determination).

On this basis, a kinetic model can be established based on sound assumptions, using the PhotoBioCREC unit data [1]:

(a)

Algal growth takes places in a well-mixed PhotoBioCREC unit. This is considered adequate given the high mixing, which is the result of the important axial and circumferentially promoted fluid motion in this unit.

(b)

The incident irradiation passing through the flow media, containing the suspended alumina particles, remains steady during the entire algal growth period. This is achieved because of the self-cleaning walls promoted by the circumferential motion of the alumina particles in the region close to the wall.

As a result, under these conditions, one can postulate with confidence that the changes in bicarbonate moles comply with the following species balance:

$$\frac{d{N}_{in}}{dt}=r_{in}{V}_f=-k_{in}{C}_{in}^n{V}_f$$

(4)

where $N_{in}$ represents the moles of inorganic carbon, $r_{in}$ is the molar rate of inorganic carbon consumption, $C_{in}$ denotes the molar concentration of inorganic species, and $V_f$ stands for the liquid hold-up in the PhotoBioCREC.

Assuming that the $V_f$ is constant, given the unchanged fluid level, and the steady visible radiation provided to the PhotoBioCREC, Equation (4) becomes Equation (5), as follows:

$$\frac{d{C}_{in}}{dt}=-k_{in}{C}_{in}^n$$

(5)

where $k_{in}$ represents the kinetic constant for the conversion of inorganic carbon species, fed as bicarbonates.

Regarding Equation (5), one can also mention, as shown later in the present study, that the sodium bicarbonate concentration displays a first-order decay ($n=1$), which is an expected order of reaction for a unimolecular species consumption.

Furthermore, while sodium bicarbonate consumption progresses, microalgae steadily forms, during a designated “growth phase.” Throughout this period, the CPCC90 Chlorella vulgaris growth can be described, using as a basis the total organic carbon (TOC), as follows:

$$\frac{d{N}_{org}}{dt}=r_{org}{V}_f=k_{org}{C}_{in}^m{\theta }_v{V}_f$$

(6)

$$\frac{d{C}_{org}}{dt}=k_{org}{C}_{in}^m{\theta }_v$$

(7)

where ${\theta }_v$ represents the microalgae matrix sites susceptible to reacting with bicarbonate inorganic molecules in a condensation reaction with the $m$ reaction order set to 1. Moreover, $k_{org}$ is the reaction rate constant for total organic carbon formation.

Furthermore, and if the bicarbonate carbon-containing species interact with microalgae sites at equilibrium, a Monod type of model results as follows:

$$\frac{d{C}_{org}}{dt}=r_{org}=\frac{k_{org}{C}_{in}}{1+K{C}_{in}}$$

(8)

Thus, Equations (5) and (8) can be used to describe the sodium bicarbonate concentration ($C_{in}$) changes, as well as the changes in microalgae-contained carbon concentration ($C_{org})$ as defined using TOC.

In addition, one can also envisage that at $K{C}_{in}\gg 1$ conditions, Equation (8) becomes a zero-order reaction. This applies for substrate concentrations at the high concentration levels used in the present study.

As a result, the following integrated form of Equations (5)–(8) can be proposed for CPCC90 Chlorella vulgaris culture in NaHCO₃ solution media:

(a)

Inorganic carbon consumption:

$$C_{in}=C_{i{n}_0}{e}^{-k_{in}t}$$

(9)

(b)

Organic carbon formation:

$$C_{org}=u\left(t-t_{lag}\right)\left\{k_{org,j}\left(t-t_{lag}\right)\left[1-u\left(t-t_f\right)\right]+u\left(t-t_f\right)C_{org}^{max}\right\}$$

(10)

with Equation (9) representing the decay of inorganic species, involving an exponential decay function; and Equation (10) representing a zero-order reaction, with a Heaviside function selected to represent the growth induction period, and the growth arrest time (Appendix D).

Furthermore, a ratio between the integrated form of Equation (7), evaluated at the maximum organic carbon concentration, and the initial inorganic carbon concentration can be established. One can obtain the maximum concentration of total organic carbon based on the initial inorganic carbon concentration as:

$$\frac{C_{org}^{max}}{C_{i{n}_0}}=\frac{1}{C_{i{n}_0}}{k}_{org}\left(t_f-t_{lag}\right)=\frac{k_{org}}{C_{i{n}_0}}\tau$$

(11)

with $\tau$ representing the growth phase time. The results obtained with Equation (11) and the parameters $k_{org}$ and $\tau$ are later presented in Section 4.2.

4. Results and Discussion

4.1. Cell Size and Biomass Composition

The CPCC90 Chlorella vulgaris cells were analyzed using a Zeiss Z1 Imager microscope. It was found that microalgae cells display a consistent quasi-spherical/ellipsoidal shape, with diameters ranging from 2 to 7 μm. This is in agreement with the data reported in the literature, where cell sizes for Chlorella vulgaris range from 2 to 10 μm [28].

Figure 2 reports the images of CPCC90 Chlorella vulgaris cells for the inoculum and for two initial inorganic carbon concentrations. One can observe that there is no significant change in the quasi-spherical/elliptical sizes, with average cell sizes consistently ranging from 4.0 to 6.0 μm with a ±0.8 μm standard deviation, as shown in the cell size distribution plot of Figure 3.

In addition, for experiments with 60 mM of NaHCO₃, SEM images of the Chlorella vulgaris cells cultured in the PhotoBioCREC unit were taken after 12 days of cultivation. A typical recorded cell image is reported in Figure 4 with the corresponding EDX elemental composition of the Chlorella vulgaris biomass.

Thus, one can observe that the CPCC90 Chlorella vulgaris cells grown in the culture, as described in Equations (9) and (10), have characteristic ellipsoidal shapes, and are composed of C, H, S, and O, as determined via combined CHNS and EDX analysis and reported in

Table 1. Elemental analysis of the cells of CPCC90 Chlorella vulgaris using combined CHNS and EDX elemental analysis. Reported results are average values between repeats with ±0.003 being the largest standard deviation.

Composition (%)	This Study	Literature [29]
	CPCC Chlorella vulgaris	Chlorella vulgaris
Carbon	55.1	46.1–50.39
Hydrogen	8.2	6.01–6.41
Oxygen 1	29.0	19.1–25.00
Nitrogen	7.1	9.01–14.77
Sulfur	0.6	0.4–6.05
Molar ratios
H/C	1.8	1.43
C/N	9.1
O/C	0.39	0.339

¹ Data calculated from combined CHNS and EDX analysis.

.

Table 1 shows that the carbon, hydrogen, oxygen, and nitrogen elemental components of the CPCC90 Chlorella vulgaris of the present study agree with the data reported in the technical literature [29]. In particular, the observed nitrogen content in the CPCC90 C. vulgaris confirmed the expected protein content [30]. In addition, the reported low sulfur content in the CPCC90 C. vulgaris grown with NaHCO₃ makes it a good biofuel feedstock [31] with low sulfur oxide emissions [30]. Finally, one can also notice the negligible sodium content in the CPCC90 C. vulgaris elemental analysis. This allows one to anticipate, consistent with Equation (3), the full sodium recycle in the CO₂ capture process.

Thus, and on this basis, a proximate formula for CPCC90 Chlorella vulgaris biomass was established as $C{H}_{1.8}{O}_{0.39}$.

4.2. Inorganic Carbon Conversion and Kinetic Parameters

Green CPCC90 Chlorella vulgaris were grown with different concentrations of NaHCO₃ species, which acted as an inorganic carbon source. Figure 5 reports the increase in inorganic carbon utilization with time as determined using Equation (2). It can be observed that the inorganic carbon conversion increased with culture time, reaching a maximum value of 27%, in the runs with 18 mM of NaHCO₃. A similar conversion of 29.6% was reached for experiments with 28 mM of NaHCO₃. On the other hand, when working with a higher concentration of inorganic carbon, the conversion into organic carbon decreased.

Thus, when feeding sodium bicarbonate to microalgae, inorganic carbon species are available for microalgae cell growth as bicarbonate $HC{O}_3^{-}$ ions. Once these bicarbonate ions diffuse through the cells, they can be converted to CO₂ in a reaction catalyzed by the enzyme carbonic anhydrase, providing the required CO₂ for the carbon fixation process [32].

Table 2. Kinetic parameters for inorganic carbon consumption.

Parameter	Value
$n$	$0.95\pm 0.09$
$k_{in} \left\{{\left({\mathrm{mmole}\mathrm{L}}^{-1}\right)}^{0.05}{\mathrm{day}}^{-1}\right\}$	$0.26\pm 0.09$

reports the reaction order and the reaction rate constant for the inorganic carbon (bicarbonate) consumption. One should note that few studies in the literature have reported the inorganic carbon conversion kinetic parameters. One should mention that the rate model obtained in our research is consistent with Jacob-Lopes, Gimenes Scoparo and Teixeira Franco [13], who reported a first-order removal of gaseous CO₂ in the aqueous phase by a cyanobacteria species.

Moreover, Figure 6a–d report the NaHCO₃ concentration changes with culture time, at four different initial concentrations, showing the good agreement between the experimental and the predicted concentrations.

Microalgae growth can be tracked using the progressive total organic carbon concentration increase with culture time.

Table 3. Reaction rate constants for total organic carbon formation and growth phase time.

Nominal Conc. of NaHCO3	${\mathit{k}}_{\mathit{o}\mathit{r},\mathit{j}}\left\{\mathbf{m}\mathbf{m}\mathbf{o}\mathbf{l}\mathbf{e} {\mathbf{L}}^{-1}\mathbf{d}\mathbf{a}{\mathbf{y}}^{-1}\right\}$	$\mathit{\tau }$ $\left(\mathbf{D}\mathbf{a}\mathbf{y}\right)$
18	0.86 ± 0.13	6
28	1.18 ± 0.05	7.2
40	1.06 ± 0.08	8
60	1.02 ± 0.11	9

reports the rate constants for the different bicarbonate concentrations, which are consistent with the already described TOC observed: (a) there is a kinetic constant increase in the 18 to 28 mM range, (b) there is a stable value of kinetic constants for 28, 40, and 60 mM of NaHCO₃. Furthermore, the reported results confirm the effective applicability of the proposed zero-order model for the biotransformation of inorganic carbon into organic matter by CPCC90 Chlorella vulgaris during the growth phase, for all bicarbonate concentrations.

Total organic carbon increased with culture time during the growth phase, with the predicted organic carbon concentration for the growth phase following the proposed zero-order model closely, during the 2–10 days period. This consistent zero-order model agrees with the Monod model, with bicarbonate carbon concentration supplied at relatively high levels [12,14,19,23,33,34].

A maximum organic carbon concentration was reached in all cases, after 8 or 11 days of algae culture. Consequently, this maximum organic carbon concentration can be influenced by the initial bicarbonate concentration, which followed a nonlinear trend, as reported in Figure 7. Therefore, the maximum organic carbon concentration $\left(C_{org}^{max}\right)$ predicted by the proposed kinetic model can be related to the initial inorganic carbon concentration, provided as NaHCO₃, using $\gamma$ and $\delta$ parameters, and estimated with a nonlinear regression as follows:

$$C_{org}^{max}=\gamma C_{i{n}_0}=\gamma C_{i{n}_0}{e}^{\left(-\delta C_{i{n}_0}\right)}$$

(12)

Figure 7 also shows the ability of the proposed model to predict maximum organic carbon concentrations using both Equations (11) and (12). Moreover, this figure demonstrates the adequacy of the calculated $\gamma$ and $\delta$ parameters estimated via nonlinear regression.

Furthermore, and regarding the selective conversion of inorganic carbon into Chlorella vulgaris, a maximum selectivity ranging from 17.0% ± 1.4% to 33.0% ± 2.0% $(Selectivity=\frac{C_{org}}{(C_{in,o}-C_{in)})}*100)$ was obtained. The selectivity decreased with the initial sodium bicarbonate concentration. These results yielded stochiometric coefficients close to $\alpha \approx 0.33$, $\phi \approx 1$, and $\beta +\omega \approx 1.67$, in Equation (3), and showed the promise of the bicarbonate conversion by Chorella vulgaris, via photosynthesis, in the PhotoBioCREC.

4.3. Kinetic Model

The kinetic modeling of microalgae allows the prediction of the PhotoBioCREC performance and the efficiency of carbon uptake by microalgae. During the lag phase, microorganisms adapt to the growth conditions (i.e., nutrients, temperature, and mixing) that can result in a partial inhibition of cell division [15]. As a result, the Heaviside step function included in the model, and presented in Equation (10), allows one to properly account for this phenomenon, predicting a close to null increase in biomass or organic carbon concentration during the lag phase. On the other hand, for the growth phase, the proposed model allows the prediction of total organic carbon concentration until it reaches the maximum value. After reaching the maximum concentration, there is a decline in the growth rate, as a result of the depletion of inorganic carbon supply.

Consequently, the kinetic model proposed in this research allowed us, in principle, to predict the CPCC90 Chlorella vulgaris growth rate, both for carbon conversion and maximum carbon fixation. In addition, and given the experimental runs developed in the PhotoBioCREC with concurrent macroscopic energy balances being established, this strategy allowed the evaluation of photon utilization efficiency, observed to be as high as 3.6% [1].

Figure 8a–d report the good agreement between the total organic carbon concentration, as predicted by the model developed in the present study and the experimental results obtained in the PhotoBioCREC prototype.

Figure 9 provides a further validation of the organic and inorganic carbon concentration model predictions, by comparing them with the experimental data. One can, on this basis, confirm the adequacy of the model proposed for the CPCC90 Chlorella vulgaris culture, ranging from 18 to 60 mM of NaHCO₃. As a result, the proposed model of the present study can be considered suitable for the prediction of carbon conversion and the prediction of the selectivity of carbon capture by microalgae.

5. Conclusions

(a)

Sodium bicarbonate solutions are valuable vectors for CO₂ capture by CPCC90 Chlorella vulgaris microalgae.

(b)

A PhotoBioCREC with controlled mixing and radiation conditions provides a suitable experimental prototype for the establishment of CPCC90 Chlorella vulgaris culture kinetics.

(c)

Measurements of bicarbonate and TOC changes with culture time show an up to 33.0% selective conversion of bicarbonates into microalgae, establishing Chlorella vulgaris photosynthesis in a PhotoBioCREC, as a promising process for carbon capture.

(d)

The developed experiments provide the needed data for the Chlorella vulgaris growth kinetic model.

(e)

The proposed kinetics allows one to predict both bicarbonate concentration changes and organic carbon concentration changes, during various CPCC90 Chlorella vulgaris growth phases, when using bicarbonate initial concentrations ranging from 18 to 60 mM.

(f)

The proposed model also reliably permits one to establish maximum CPCC90 Chlorella vulgaris concentrations values, for various initial bicarbonate concentrations.