You are on page 1of 16

Energy Nexus 4 (2021) 100032

Contents lists available at ScienceDirect

Energy Nexus
journal homepage: www.elsevier.com/locate/nexus

Review on the recent structural advances in open and closed systems for
carbon capture through algae
Swastik Paul1, Souhardya Bera1, Rishav Dasgupta, Shibsankar Mondal, Subhasis Roy∗
Department of Chemical Engineering, University of Calcutta, 92 A.P.C ROAD, Kolkata 700009, India

a r t i c l e i n f o a b s t r a c t

Keywords: Carbon capture has already been at the forefront of fighting global warming and ascending carbon dioxide emis-
Carbon capture sions. To cumulate for a net-zero world by 2050, scientists believe carbon dioxide sequestration to play a con-
Microalgae cultivation sequential role. For achieving this near impossible, technologies ranging from simple chemical absorption and
Open raceway ponds
adsorption to novel membrane and biological methods have been studied. This review paper focus tentatively on
Closed systems
one of the many carbon capture methods- the biological algal systems. Algae has nearly forty times the photosyn-
Photobioreactors
Microalgae carbon capture thesis rate than normal terrestrial organisms, and a circular bio-economy involving algae lead to diversification
Biomass production of feedstock and raw materials. After a short overview on the requisite for carbon capture and other technologies,
the article discuss the general strategies for macroalgae and microalgae mediated systems and their applicabil-
ity. Recent developments in the open raceway pond systems and the closed photobioreactor systems have been
reviewed extensively, and novel strategies have also been focused on. A brief discussion has also been added to
understand the relation of carbon capture technologies and their implications on the Energy-Water-Food nexus.
The present article also discuss the future roadmap for new research and development works that need to take
place and how the integration of certain different subjects can render microalgae as a prosperous commercial
feedstock.

1. Introduction dioxide emissions and need to be phased out as quickly as possible. As


a result of uncontrolled human activities over the last 150 years, atmo-
Global warming is one of the major issues for many countries around spheric levels of CO2 have increased by nearly ∼25%. It seems impos-
the world. Climate change is more a ‘threat’ than being a ‘change’. Even sible to scale out fossil fuels within the time scale of climate change.
if a tentatively small review is carried out, the issue continues to grow Studies depict that in a rush to return businesses to pre-covid levels,
as a critical one, for the impact of human intervention on the climate, global emissions have been on a rise, with emission reduction targets
particularly colossal-scale deforestation related activities and burning being severely compromised. The rise in the global energy CO2 release
fossil fuels, that have grown manifold since the advent of the industrial has been as much as nearly 2% in the space of one year between Decem-
revolution, and currently still releasing enormous magnitudes of green- ber 2019 and December 2020 [5]. Fossil fuels burn to produce flue gas.
house gas [1]. The global average surface temperature of the planet has Flue gas emitted from the burning of coal mostly contains carbon diox-
risen by 0.78 °C from 1900 to 2005 and consequently as forecasted by ide (CO2 ), sulfur and nitrogen oxides (SOX and NOX ), nitrogen (N2 ),
the Inter-governmental Panel on Climate Change (IPCC), a rise of 2–6 °C oxygen (O2 ), and water vapor. But even then, CO2 forms the largest
can be expected by the end of this century. Fig. 1 shows the percentage of component of flue gas [6]. Even at this point, it is worth mentioning,
global carbon emission by countries around the world in the year 2019 that nearly a quarter of greenhouse gas emissions from land use, agri-
[2,3]. Even recently even IPCC had coded the climate change as Code culture, forestry is rarely considered. Additionally, there are industries
Red, which requires drastic measurements to combat climate change. where the production of CO2 is unavoidable, and therefore moving to
As Goldemberg had mentioned- “Fossil fuels cannot be considered the net-zero forum require a major overhaul in process intensification.
the world’s main source of energy for more than one or two genera- There is only a fixed amount of carbon dioxide that the world can emit
tions” [4], fossil fuels continue to power some developed, and majority to maintain global warming below a certain temperature limit, termed
of the developing countries. Data by the International Energy Agency the carbon budget. At the present rate of emissions, it be very difficult
(IEA) shows how developing countries form the major chunk of carbon to tackle emissions within the budget for a 2° C rise in global temper-
atures, which can still be compensated, if it can be managed to work
on negative emissions for the next half of the century. But it is always

Corresponding author. better to remove and adjust emissions at the source than pursue capture
E-mail address: srchemengg@caluniv.ac.in (S. Roy). techniques when CO2 is at its lowest concentrations. And therefore, to
1
Authors Swastik Paul and Souhardya Bera have contributed equally work.

https://doi.org/10.1016/j.nexus.2021.100032
Received 17 September 2021; Received in revised form 17 November 2021; Accepted 28 November 2021
Available online 30 November 2021
2772-4271/© 2021 The Author(s). Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license
(http://creativecommons.org/licenses/by-nc-nd/4.0/)
S. Paul, S. Bera, R. Dasgupta et al. Energy Nexus 4 (2021) 100032

Fig. 1. Global carbon dioxide emissions by different


countries in the year 2019.

reduce the amount of CO2 in the air, people around the globe are trying than usual terrestrial plants, for their greater capacity to capture light
numerous methods to capture and utilize carbon dioxide, from any and and convert to usable energy [23,24,25].
every source possible. Although microalgae reside in aqueous environments, they have
A severe detrimental geochemical process that is often skipped is driven a similar photosynthetic process as in higher plants [26], where
ocean acidification, although oceans account for 25% of anthropogenic directly passing CO2 -rich gases through their culture be a very efficient
carbon dioxide emission captures [7]. Excess amount of CO2 causes the way of capturing CO2 . Algae can grow fast and require a concentrated
rise in production of H2 CO3 (or, carbonic acid), which then dissociates source of CO2 for photosynthesis, given which has a very high energy
into H+ positive ions and CO3 2− negative ions expeditiously. This causes conversion efficiency. Moreover, they also have a carbon-concentrating
a decrease in pH from a normal of 8.1 to lower values, with paramount mechanism that suppresses photorespiration [27,28]. Algae-based CO2
implications on marine life and other biogeochemical cycles. capture is therefore becoming one of the viable options for anthro-
Carbon Capture and Utilization (CCU) sims not only truncate the pogenic CO2 conversion.
volume of atmospheric emissions but also achieve a benefit through the Algae contain lipids (7–23%), carbohydrates (5–23%), proteins (6–
use of CO2 for various industrial processes superseding conventional raw 52%), and some percentage of fat. Although it varies with species,
materials [8]. This help facilitate the transition from low-carbon energy most of the constituents can be converted for numerous commercial
production to capture and utilization while keeping emissions for large applications, such as human food, medical drugs, cosmetics, biofuels,
emitters like steel, cement, thermal power stations under careful con- biomolecules, and bio-fertilizers for specific applications. Additionally,
trol for a move towards net-zero carbon emissions by 2050. The major microalgal cells can be considered cell-level sunlight-driven factories,
virtue of CCUS is that it is quite versatile, incorporating a fairly large which are capable of converting captured CO2 to biofuels, animal food,
number of technologies applicable to multiple industries. CCU describes chemical feedstocks, and bioactive compounds of high value [29,30,31].
the capture of CO2 from the power plant and industrial emissions and For the power generation industry, these algae applications [32] are a
utilizing it to produce value-added products. CO2 utilization can gener- bonus after capturing CO2 from coal combustion. While Algal cultiva-
ate revenues which can contribute to offset costs associated with CO2 tion is expensive, algae biomass as feedstock can be utilized to produce
capture. captured carbon dioxide can find potential applications in: diverse products generate revenues, thereby rendering this route plau-
sible.
i. Enhanced Oil Recovery (EOR) [9,10,11]
ii. Feedstock for production of urea, ammonia [12], carbonates [13,14] 2. Past work and novelty in the present review
etc.
iii. Feedstock for production of methanol [15,16], dimethyl ether Microalgal carbon capture had found immense consequentiality as
[17,18], syngas [19] etc. which may be done in combination with to capturing carbon dioxide and how important it is to produce biofuels
renewable sources, most likely with solar cells, which have had very to achieve a net-zero carbon society by 2050, and restrict temperature
good development over the last decade [20]. rise to 2° Celsius. A lot of work had been reported in the field, with very
iv. CCU in mineralization in the cement industry [21]. high-quality reviews present, highlighting important studies in the field
[33,34,35].
CO2 utilization provides excellent opportunities for investment in in- To understand the evolution of study in the field of microalgae me-
dustrial developmen t, innovation, and manufacturing, and is undoubt- diated carbon capture, we searched for the number of articles published
edly a captivating alternative to Carbon Capture and Storage (CCS), over years in the science direct database with the title- “Carbon cap-
given there are required economic incentives to invest in such projects ture by microalgae” (dated: August 01, 2021) shows Fig. 3. It is erst-
[22]. It is extremely necessary to maximize synergies between CCS and while to note that the total number of studies have increased post-2015,
CCU technologies to achieve the calibers of decarbonization required which can be understood from the strong stance taken by governments
to meet international climate goals. The different carbon dioxide cap- to tackle the problem of rising carbon emissions and move towards a
ture techniques researched and used in commercial operations shows in more carbon neutral-net zero society. The problem associated with ac-
Fig. 2. cepting carbon capture technologies had been the cost associated and
Algae, considered to be one of the simplest and ancient of the photo- the economics of the processes have not been specified yet. But since
synthetic plants that grow in the aquatic systems, are distinguished for the cost of capture is not only attributed to only the process, but spread
their superior growth rate and carbon capture capacity compared with over the whole flow diagram, from feedstock collection, process design
other plants. Algae tend to have a higher photosynthetic competency and specification, and finally production of required products or storage

2
S. Paul, S. Bera, R. Dasgupta et al. Energy Nexus 4 (2021) 100032

Fig. 2. Different technologies for CO2 separation and capture.

Fig. 3. A comparison between the number of papers published each year as indexed in Science Direct.

in an underground reservoir, thus a need for optimization rises in the ternatively target high productivities with similar or lower production
algae industry [36]. costs [40]. The genetic and metabolic alterations can potentially target
A fraction of past review papers have discussed the possibility of to enhance the fixation pathway or in certain cases create additional
genetically mutating different strains of microalgae to provide higher pathways for increased carbon dioxide uptake at higher efficiencies. A
CO2 tolerance, optimal use of nutrients and waste as feedstock, and more exciting prospect can be optimizing the performances of the en-
proper resistance to uncomfortable thermal and ionic parameters. Avail- ergy harvesting complexes [41].
able strategies like random mutagenesis, which includes the likes of nu- A major part of the review papers discusses the concept of a bio-
clear radiation mutagenesis, chemical mutagenesis, and UV mutagene- circular economy that can be formed around microalgae as the central
sis. More prominent ones like adaptive evolution help cultivate specific source of feedstock for biotechnical applications, involving renewable
strains with desirable characteristics in previously specified conditions biofuels, and bioactive compounds like nutraceuticals and cosmetics.
[37]. The prospective of genetic and metabolic engineering is especially Being a very new center for being a ‘circular economy’ feedstock, scien-
interesting as they tend to provide better efficiencies in identically struc- tists believe it still can unlock new potential applications in bioactivities
tured cultivation systems, with approaches to work on protein or genetic and waste management [42,43]. The studies signify that algal species
modifications and modify the biochemical process [38,39]. This can al- are a major part of the solution to mitigate the problems of the energy

3
S. Paul, S. Bera, R. Dasgupta et al. Energy Nexus 4 (2021) 100032

crisis, global warming, and water pollution. Thus, they tend to capture Scientists predict that coal gasification and gas reforming has already
the bio-cycle approach which is required for algae to be incorporated in been perfectly developed, and very advantageous for the high carbon
a biorefinery system [44,45]. A singular stand-alone microalgae biore- content pre-combustion, but still, the technology suffers from high pro-
finery system could be beneficial to produce economically important cess costs [63].
biofuels and sustainable products, although an integrated power plant-
biorefinery system be more economically feasible and competitive in re- 2.3. Oxyfuel combustion capture
gards to a CCS system [46]. Even, most were vastly focused on biofuel
production [47,48], such as its use as a feedstock to alleviate the biofuel The process mentions high purity oxygen to be used in lieu of air
crisis. A holistic approach can be found in several papers, which dealt for combustion. But, the oxy-fuel process requires rearrangement of the
with the research and development disciplines, in addition to defining base design of power plants before the combustion takes place, as well
the improvements as a sustainable resource [49,50], and understanding as renewed designing of the boiler. When the fossil fuels are burned in
the thermochemical process advancements [51]. Case studies of differ- presence of oxygen the flue gas consists of a high amount of CO2 , water,
ent countries with specific policies also focus to encourage the devel- particulates, and SO2 . So, there is a substantial reduction of toxic gasses
opment of biofuels, with specific mentions about how the developed such as NOX for nitrogen is the major component removed in the oxy-
policies should have a global outlook [52,53,54,55,56,57,58]. fuel method before combustion takes place. SO2 and particulates can
Although every paper includes a part of their discussion on the cul- be removed by flue gas desulphurization and electrostatic precipitation
ture strategies, there are very few reviews on the construction and un- respectively [64]. Water present can also be separated by simple me-
derstanding of how these functions. These tend to study the system only chanical drying of the gas. So, the resulting flue gas just contains high
to inform about the types. Very few reviews dig deep into the whole de- concentrations of CO2 (80–98%) only, which can easily be captured. Ad-
velopment of the systems and the intricates [59,60]. But then it is very ditionally, the absence of nitrogen-containing compounds reduces the
important to understand the constructional features of systems than just infrastructural development required for flue gas treatment.
studying what the system consisted of, and this field has been highly de- Due to the presence of a high concentration of carbon dioxide, effi-
luded in terms of study and reviews [61]. Herein run through the rudi- ciency remains usually high, supported by well-developed air separation
ments of carbon capture starting essentially from the basics of carbon techniques. But high corrosive nature and cost inefficiency limit its de-
capture and then focusing on the macroalgae and microalgae mediated ployment [65].
carbon capture. The focus be on different recent developments in the Increased deployment of renewables in the energy sector is a crit-
open and closed system, and how different strategies can be applied ical factor for incorporating CCU systems in power plant operations.
in the field. The systems be discussed rigorously with the exhaustive With more renewables lined up to be installed to cater to the rise of de-
description provided to understand each result. The review paper adsc- mand in energy, thermal power plants need to be increased flexibility
ititiously relish highlighting a future roadmap in the field, and how the to operate under seasonal variations in requirement. Since renewables
gradual incorporation can commence with the data already in hand. still require more development for use at the highest scales around all
seasons, till then retrofitting CCUS technologies to fossil fuel-powered
2. A brief overview of all carbon capture techniques thermal power stations provide this flexibility to ensure a stable energy
supply. Long-term seasonal variation is a major challenge, for renew-
The carbon capture techniques can be classified into pre-combustion ables, and CCU facilities with thermal generators can play an important
capture, post-combustion capture, and oxy-fuel combustion [62]. role in the balance. This can also promote economic advantage at times
of low energy requirement from power plants.
Aside from these, many other biological routes [66] can be taken to
2.1. Post-combustion capture capture carbon dioxide such as

In this route, CO2 is extracted from the flue gas after the burning of (a) Afforestation i.e., planting trees and forests so that they can use car-
fossil fuel and therefore does not require any transmutations to be made bon dioxide in the air to produce oxygen thus reducing the concen-
to existing power station structures. This is especially important since tration of carbon dioxide in the air.
the lifespan of any power generating station are very high, and so the (b) Using renewable energy (or to a certain extent, carbon-negative en-
replacement rate is low, with the associated financial costs of replace- ergy sources) such as hydro, wind, solar, and biofuel to run vehi-
ment high. So, carbon capture post-combustion is an important CC tech- cles instead of petrol and diesel which produces a lot of carbon
nology implemented across countries. The processes that are involved dioxide when burned, although some of them are only near zero-
in post-combustion capture are adsorption, chemical absorption, cryo- carbon emission fuel, whereas few requires incorporated CC systems
genic separation, and membrane separation technology. Projects like to reach net-zero carbon emission fuels.
the Boundary Dam and Petra Nova projects are already in service, and (c) Biological sequestration- Ocean fertilization, algae cultivation, and
further cost reduction is possible by increased deployment or the use of blue carbon nature restoration is mainly happening due to its effi-
other innovative solvents. ciency in capturing carbon dioxide, and alternatively, for its nature
conservation initiatives.
2.2. Pre-combustion capture Certain advancements that are made in recent times are as follows
Currently the separation techniques of carbon dioxide from flue gas
The method describes CO2 being captured from fossil fuels before (mainly by absorption, adsorption, and membrane separation) had some
the combustion takes place. This process mainly involves the gasifica- efficient growth.
tion process done in a gasifier under a low oxygen level forming a syngas Singh et al. has provided a very elaborate comparative and descrip-
from coal which mainly contains CO and H2 O (free from pollutants) and tive table on the various carbon capture techniques, their mechanisms,
this syngas undergoes water gas shift reaction with steam producing H2 advantages, and disadvantages [67].
and CO2 . Therefore, H2 becomes the fuel-producing electricity in the
turbine. But the design requires making radical changes to the present 3. Why algae?
power-generating stations, and so is limited to new-build power sta-
tions. Although the power input into the pre-combustion system can be Algae are multicellular or unicellular organisms whose growth is
deemed analogous to coal-fired power stations, it is much less efficient based on the photosynthesis mechanism; they account for more than
when compared to gas-fired power stations. 50% of global organic carbon fixation [68]. Just like plants they also

4
S. Paul, S. Bera, R. Dasgupta et al. Energy Nexus 4 (2021) 100032

Table 1
Advantages of microalgae and macroalgae towards carbon capture system.

Microalgae Macroalgae

• A sustainable process that reduces the carbon footprint • Reasonable carbon capture capacity
• Has high conversion efficiency • Bioremediation of contaminants
• High photosynthesis rate [69] • Higher net productivity
• Rapid growth rate [70]
• A highly efficient process with low operation cost
• Carbon losses are minimal and have good adaptability to
the environment

use carbon dioxide and light energy to produce oxygen and sugar. They ing to carbon capture, macroalgae suffers from inadequate CO2 level
are mostly found in water and aquatic organisms mainly eat algae as as a primary factor for macroalgae biomass production. Although there
their main food. Of the two basic types of algae- (a) microalgae and have been studies to extensively understand the carbon preferences, and
(b) macroalgae, microalgae find more extensive use than macroalgae how the amount of carbon affects macroalgae growth, the use in marine
in the field of carbon sequestration. The advantages of microalgae and macroalgae has not yet been quantified. Macroalgal species can be inte-
macroalgae towards carbon capture system are shown in Table 1. grated with coal and oil-fired power stations to produce biomass feeding
Microalgae can be used as food, to get useful proteins. They are also on both wastewater and flue gas, consequently producing bio-oil and
regarded as an alternative to future renewable energy sources. Microal- other associated products, with the major advantage that macroalgae
gae is very important in capturing CO2 from the flue gas due to their have higher productivities and carbon capture efficiency [80].
small size property to control in a close system and its byproducts are
used for producing biofuels and various cosmetics, medical drugs, etc. 4. Mechanism of CO2 capture by microalgae
It is essential photosynthesis, which uses water and CO2 to produce
organic compounds without the consumption of any secondary energy The simple presence and occurrence of photosynthesis in the algal
source. Its high photosynthesis rate [71] (at times nearly 40 times more species define the demand for chlorophyll and CO2 . Similar to all ter-
than terrestrial counterparts) is well supported by a rapid growth rate, restrial and chlorophyll-possessing plants, atmospheric CO2 is the pri-
good environment workability, eco-friendly and low cost of operation mary source of carbon required for photosynthesis- the reason for higher
[72]. Essentially, it is the lipid content in microalgal species that are cell densities and increased metabolism rate. This occurs by undergoing
responsible for food and fuel production in the future. The advantage mainly two stages. The first type is the light-dependent stage and the
is that they can be cultivated without following traditional agricultural second one is a sequence of light-independent reactions. Fig. 5 shows a
procedures and under any water conditions (waste-water, sea-water, or tentative carbon dioxide flow within any microalgal species.
pure water) provide microalgae an edge over their terrestrial counter- The principal objective of light-dependent processes is to supply
parts. Moreover, there is no additional drawback related to food secu- the biochemical reductant nicotinamide adenine dinucleotide phos-
rity, land use, and water scarcity. Additionally, they don’t require high phate (NADPH2 ) as well as the chemical energy, adenosine triphos-
purity of CO2 to grow, and combustion products in the case of flue gas phate (ATP), required for inorganic carbon absorption. Two electrons
being used act as nutrients to the system. Aquatic microalgae are ideal in are taken from water molecules in this cycle, resulting in the release of
the production of liquid fuels since they can be consumed as sustainable, O2 , which is then transmitted through an electron transport chain, cul-
environmentally friendly carbon-neutral fuels for their fast growth, en- minating in the synthesis of NADPH2 . Protons are transferred from the
hanced biomass yields, variety of products, and their extremely simple stroma into the intrathylakoid region at the same time, resulting in a pH
harvesting methodology in ponds and closed bioreactor systems [73,74]. gradient. In a mechanism known as photophosphorylation, this gradient
Fig. 4 shows a general schematic of how microalgae is cultured and cul- stimulates ATP production, which is mediated by ATPase [81].
tivated to process bio-based product or convert to energy. light energy∕chlorophyll
Inherently, the algae system can be a part of the biomass-derived 2NADP + 2H2 O + 2ADP + 2Pi ←←←←←←←←←←←←←←←←←←←←←←←←←←←←←←←←←←←←←←←←←→
← 2NADPH2 + 2ATP + O2
circular bio-economy, with waste products, side-residues, and industrial
This stage passes through several photosynthetic reactions in absence
wastes being important raw materials in the system. It help in the zero-
of light. Carbon assimilation and photorespiration are the key reactions
waste initiative, also helping in diversification in feedstock, leading to
here. The carbon assimilation step is the process of CO2 ¬fixation using
a successful commercial market [75]. Even after varied interests, CCU
NADPH2 and ATP produced in the light-dependent stage. This mecha-
involving microalgae is not considered competitive, and major contrib-
nism was discovered by Calvin and Benson. [82]
utors to the capital requirements are equipment and labor costs. Com-
NADPH2; 3ATP
petitive strains need more focus to divulge a more competitive and ap- CO2 + 4H+ + 4e− ←←←←←←←←←←←←←←←←←←←←←←←←←←←←→
← CH 2 O + H2 O
propriate microalgae-mediated future [76].
Macroalgae-both cultivated and wild-grown prove to be a consider- Micro-algae have been found to possess carbonic anhydrase (CA),
able sink for anthropogenic CO2 emissions, and proper use of macroal- which is a zinc-containing metalloenzyme that helps in carbon capturing
gae could make it a considerable choice to vent out carbon and green- by catalyzing the reversible hydration of CO2 into bicarbonates and a
house emissions [77]. The species are already well-established bioen- proton which further helps in CO2 capture from the air [84]. It speeds
ergy options, with anaerobic digestion and fermentation frequently car- up the equilibrium between CO2 and HCO3 − at physiological pH [85].
ried out. But, tests for biofuel production from seaweeds have not been CO2 + H2 O ↔ HCO−
3 + H ↔ CO3 + 2H
+ 2− +
high. Even then, the major advantage it provides is its high produc-
tivity even in areas that are non-arable and nutrient-deficient, thereby The CA enzyme converts the Bicarbonates to CO2 so that it can be
avoiding the much-heated food v/s fuel debate. Ocean macroalgae is an acted upon by the primary carbon fixation enzyme Rubisco (Ribulose-
organism with high carbon capture potential, converting high levels of 1,5 bisphosphate carboxylase/oxygenate). But, since both CO2 and O2
inorganic carbon to biomass [78]. Carbon capture adds to the marine are substrates for carbon fixation, it is in direct competition with pho-
bio-refinery concept and therefore, both optimized can have a power- torespiration. The carbon concentration mechanism (CCM) acts as an
ful effect on capture potential in such algae refineries [79]. But com- additional enhancer of CO2 for the Rubisco enzyme [86]. This strategy
depends on the form of carbon being taken up by the algae. Since carbon

5
S. Paul, S. Bera, R. Dasgupta et al. Energy Nexus 4 (2021) 100032

Fig. 4. General flow diagram associated with cultivation and


use of microalgae for carbon capture and fuel conversion.

Fig. 5. A tentative carbon dioxide loop in microalgae


species. [83] (Reprinted with permission. Elsevier).

dioxide concentrations play a major role in the growth and metabolism around the year. The only problem can be lack of availability of sunlight
of microalgae, a continuous supply of it is maintained by Rubisco, which during night time. However, the use of artificial lighting might help in
depends on the rate of CCM and CA metabolism. Hence, CA and Rubisco counteracting this problem at a higher energy input cost but it will fa-
concentrations also turn out to be a controlling and limiting factor in cilitate continuous production [87].
metabolism. Not only have micro-algae been found to be effective in carbon cap-
The idea is to use the biological process of photosynthesis in mi- ture but also the products obtained after this capturing are of great eco-
croalgae to capture CO2 and convert it into products that have some nomic value and the possibility of their conversion into more important
economic value. In photosynthesis, CO2 , used as raw material and in products makes the idea of the use of micro-algae for carbon capture
presence of water and sunlight, is converted to glucose and oxygen. Sun- all the more lucrative. Microalgae produce a good quantity of lipids in-
light is abundantly available in almost all corners of the earth and all side the cells and these lipids can, in turn, be converted into products

6
S. Paul, S. Bera, R. Dasgupta et al. Energy Nexus 4 (2021) 100032

Table 2
A comparison of the open and closed microalgae cultivation system.

Cultivation type Advantages Disadvantages

Open • Economical • Difficult to control growth parameters


• Easy operation • Fixation rate low
• Easy scale-up • Large area required
• Requires no specific nurture conditions • Contamination rate high
• Less energy requirement • High evaporation losses
• High stability • Low biomass productivity

Closed • Good control over process parameters • Biofilm formation on the interior side
• Fewer contamination risks • Scale-up difficult
• A very low initial investment • Large shear forces
• No evaporative losses

like biodiesel, gasoline, green diesel, pseudo-vegetable oil, etc. The ap- Several techniques have been discussed below for the large-scale cul-
proximate micro-algal cell carbon content is about 50 % by dry weight tivation of microalgae. But, previous to that, it is necessary to under-
[88] out of which approximately 1.8 kg CO2 can be fixed 1 kg of micro- stand the advantages and disadvantages of the closed and open system,
algae biomass [89]. Microalgae have also been found to fix CO2 with although a very good comparison is also available by Znad et al [98].
an efficiency that is 10–50 times more effective than terrestrial plants. Table 2 furnishes a general comparison between open and closed mi-
gases like Sulphur and Nitrogen Oxides which are sometimes produced croalgae cultivation techniques usually employed.
with CO2 have been seen to have nutritional value for microalgae and
also microalgae do not always require pure CO2 which is why flue gas 5.1. Open systems
containing CO2 can be directly used without the use of scrubbers. The
presence of SO2 is found to have a strong inhibitory effect on microalgae These are simple and facile to build systems like ponds and tanks,
growth, with concentrations above 100 ppm, microalgae cultivation be- where the algae are allowed to grow and conventionally under natural
comes difficult [90]. The H+ released during hydrolysis of SO2 results in sunlight. However, CO2 fixation is customarily low and requires some
an increase in acidity, causing an inhibitory effect on microalgal growth. artificial lighting at night to be able to fix CO2 even in the absence of sun-
The decrease in pH can be understood to be the case for inhibition and light. Consequently, it is difficult to maintain the requisite environmen-
thus, in cases where pH is maintained artificially, microalgae growth tal conditions, such as pH, temperature, and mixing intensity. Contami-
seems normal [91]. But, SO4 2− and HSO4 − can in some cases be also nation of other algal species and external organisms causes low biomass
found to have an inhibitory effect [92]. NOx concentrations have a con- productivity, sometimes toxic and unusable. Seasonal variations addi-
trasting behavior at low concentrations and higher concentrations. At tionally affect biomass productivity in cases [99,100,101]. The depth
extremely low concentrations, it transforms in NO2 − which is a form of of the open system is usually limited as sunlight can only penetrate a
nitrogenous nutrition [93], whereas, at concentrations above 300 ppm, certain distance [102]. Examples of open systems include: -
they inhibit microalgal growth [94].
A recent study has indicated using a microorganism-microalgae 5.1.1. Simple pond
co-culture system (fungi-bacteria-microalgae) for enhancing photosyn- These are most simple and economical both in management and
thetic performance and capture efficiency. The metabolism was found construction of algae in open. Sometimes a rotating mixture might be
to greatly increase and capture efficiency (73.54±6.83% removal effi- there to inhibit algal precipitation. Although they are cheap to build
cacy) was enhanced, though to be the effect of strigolactone (GR-24) on and known for their simplicity of operation and ease of scaling up, it
the symbionts and microalgae [95]. is difficult to control the growth parameters like contamination of wa-
All these factors make the use of micro-algae in carbon capture ter and temperature. Contamination can even occur due to rain where
highly lucrative and make us even more optimistic towards the idea other strains of micro-organisms can contaminate the culture medium
of achieving a green economy. and that might hinder the growth of desired algae. As a solution, mi-
croalgae species that can survive saline or extreme alkaline environment
5. Microalgae cultivation technique can be decided to be grown.

The potential of deriving valuable substances from micro-algae has 5.1.2. Open raceway pond (ORP)
caused researchers to envision the possibility of using them as a source Some alterations can be done to the simple pond to make a race-
from where those materials can be derived. The cultivation techniques way pond (looks like an automotive raceway circuit) which comprises
can be chosen as per (a) the source of nutrients, which is a very im- most of the open pond systems developed for carbon sequestration. The
portant factor for algal growth, (b) the desired products, and (c) the ORP is usually made up of either plastic or concrete and either they are
investment cost. However, commercial production of those products re- located on the ground or they are dug on the ground. In case of dig-
quire large-scale cultivation of the micro-algae to derive the products ging, the walls have to be lined up for preventing the percolation of
in sufficient quantity. An ideal microalgae culturing system should pos- water into the soil. The constructional morphology finds a direct cor-
sess the characteristics including (1) adequate light source, (2) effective relation with biomass production, nutrient uptake, and fixation rate.
transfer of material across the liquid-gas barrier, (3) simple operation The cultivation mixture is forced in a particular direction to keep the
procedure, (4) minimal contamination rate, (5) cheap overall building algae suspended in the raceway pond, i.e., mixing is an important pa-
and production cost, and (6) high land efficiency [96]. Hence, the loca- rameter to understand mass transfer rates in the system [103]. This is
tion of the cultivation is an integral factor of the climate and weather done with the help of a paddle-wheel to keep the direction of water
conditions around the year, and other required entities for the success- flow fixed [104]. These systems provide better control but the huge area
ful growth of microalgae with the highest biomass productivity. But, it’s that is required to grow the algae might cause a hindrance to the path
understandable that carbon capture from microalgae in any condition of their commercialization. Chlorella, Spirulina, etc. are the species of
is economical since algae can capture around 90% of CO2 under closed micro-algae that can commonly be grown in this method. It is also pos-
conditions and up to 50% in open structures [97]. sible to do the same in wastewater and on top of this, it can also be

7
S. Paul, S. Bera, R. Dasgupta et al. Energy Nexus 4 (2021) 100032

Fig. 6. A schematic of the design of an ORP showing the (a) top view, (b) front view, (c) right side view and, (d) the paddle wheel design. [117] (Reprinted with
permission Elsevier).

combined with the carbon capture technology in thermal power plants.


But ORPs suffer from low biomass productivity [105] and low residence
time of CO2 fixation, and additionally from evaporative losses, which
can be attributed to local climatic conditions [106]. Biomass productiv-
ity is found to have an exponential temperature dependence, that too up
to a certain temperature with productivity reducing thereafter. 25–350
Celsius can be taken as optimal growth temperature zone for species, al-
though marine species suffer from permanent cell damage and lessened
Fig. 7. Vertical column Bioreactor [138] License CC by 4.0.
productivity at temperatures above 28° Celsius. Seasonal variations also
impact the productivities and growth rate of biomass in ORPS. Summers
tend to have higher productivity when compared to the winters or the
incorporation of flue gas (FG). Both the ORPs were operated at a fixed
spring-autumn season [107]. High light intensity also causes the death
depth of 0.16 m and with a working volume of 60 L of the microalgal
of certain cultivable species due to the degradation of chlorophyll II,
culture solution. A paddle wheel was used at 16 rpm and the linear cir-
which can adversely affect microbial growth and cause photoinhibition
culation rate was kept at 30cms−1 . Gas spargers at equidistant points
[108]. Where high light intensity increases photosynthesis is highly vis-
ensured flue gas delivery at three equally aerated delivery zones. With
cous culture, less absorbance of light in dense mediums decreases pho-
the FG, they found a 3.5 times improvement in biomass productivities
toinhibition and increases productivity. In cases, light guides can help
under the semi-continuous mode but found that the microalgal culti-
increase light distribution and enhance the fixation rate of carbon diox-
vation entered a stationary phase, due to carbon source limitation and
ide in the culture [109]. CO2 supply plays an important role in bridging
reduced light penetration at high cell densities. Growth kinetics with FG
carbon demand in productivity and balancing carbon emissions to the
incorporation also depended on the irradiance period. They also noted
environment. The CO2 supply and efficiency depend on the mass trans-
that temperature and its fluctuations exerted certain problems with the
fer coefficient, mixing capacity, sparger type, the contact time in the
evaporation and biomass productivity concerned. However, the semi-
ORP, and pH, which should be optimally set and maintained [110]. The
continuous mode also proved to be a better model of operation with flue
CO2 mass transfer is critical to understanding the amount of CO2 to be
gas passed through it, which additionally showed better performance in
supplied and the economics it allows for. It is therefore of utmost impor-
terms of carbon footprint in the life cycle assessment, if merged with
tance to work for better mass transfer which depends on various fluid
any thermal power plants [117]. The researchers although receiving an
mechanical properties in the ORP [111,112]. The most preferred and
anticipated result concluded that there was a requirement for the whole
usually optimal pH remains around 6–8.76, which is preferred by most
energy to be more efficient, with the technologies and operation effi-
of the cultivated microalgal species [113]. The pH does not remain a
ciency more improved for an open system (Fig. 6).
major challenge for the capture of atmospheric CO2 but possesses grave
Advanced technologies and the use of the Internet of Things (IoT) to
challenges when under the effect of industrial flue gas, which contains
sustainably design a smart microalgae ORP, with a fixed pH controller
NOx and SOx emissions too. Reports also state that the varying amounts
and incoming light intensity. The CO2 supply could also be controlled
of CO2 in industrial flue gas emanating from different industries allows
to have an optimal photosynthetic and respiration rate for enhanced
for maximum productivity at different pH values [114,115]. Therefore,
biomass productivity, as both low and high CO2 concentrations lead
understanding biomass productivity at different pH values is important
to unnecessary growth inhibition, and the effect of the same amount
[116]. Even then, a balance needs to be established between CO2 mass
of concentration may conventionally vary the productivity in different
transfer rates and biomass productivity.
species. Paddle-wheels, which play an important role can controlling
Yadav et al. had tested an ORP system at Kharagpur India, developing
sunlight radiation for better growth and metabolism. The speeds can
a system on both batch and semi-continuous mode, with and without the
also be changed with the intensity of sunlight that is being received,

8
S. Paul, S. Bera, R. Dasgupta et al. Energy Nexus 4 (2021) 100032

further increase in its capture rate and biomass production. A summary


of the ORP systems discussed has been provided in Table 3.
Limited light penetration is a major reason why most of the con-
struction of most ORPs is often shallow. Computational Fluid Dynam-
ics (CFD) studies have been very beneficial lately to help give an idea
about the ORP dead zones, shear stress, power consumption, and other
hydrodynamic properties [127]. A strategy to mitigate the problem of
low biomass productivity in ORPs may be to construct a deep ORP in-
Fig. 8. Horizontal tubular bioreactor [139] Reprinted with permission. corporated with a transparent light scattering column (LSC). The LSC
is originally aimed to deal with the absence of light at deeper levels of
ORP, but this might additionally mitigate the problem of evaporation
losses. A similar model of operation by Sirikulrat et al. showed where
biomass productivity increased by about 48.3%, the evaporative losses
decreased by 13.6% for the cultivation of Spirulina [128]. It also affected
the cultivation period of the stationary phase and the net energy ratio,
thus providing an acceptable method to ORP problem mitigation. An-
other novel strategy can be using up-down chute baffles. This generates
alternate clockwise and anti-clockwise motion, which affects certain in-
fluential properties of the culture. This alternate vortex flow was impe-
rial to enhance the vertical fluid velocity, which was alternatively the
reason for the decreased dark-light cycle period of 1/12. There was also
found to be a 25% increase in the mass transfer coefficient because of
the sequential alternate motion [129].

Fig. 9. A schematic of bubble column PBR [140] Reprinted with permission. 5.2. Closed system

Closed systems or what is referred to as photobioreactors (PBRs) are


systems that prevent the direct exchange of gases between the system
and the environment and also prevent contamination.
They can provide more control over parameters like temperature,
pH and rate, and contamination due to other gases as the gas is usually
passed through a sterilized gas filter before being fed to the algae.
Closed raceway ponds (CRWP) are sometimes tested for high per-
Fig. 10. Flat type PBR [141] Reprinted with permission. formance to mitigate the intrinsic quandaries of an open system, and
incorporate the advantages of the closed-loop of reactors. But careful
calibration needs to be carried out in the mode of CO2 supply. Studies
therefore at night the paddle-wheel automatically stops. IoT also can found a strong correlation between the mode of supply-either contin-
control the CO2 inflow rate based on the pH and water speed. The in- uous or intermittent. Li and his group found that intermittent opera-
tegration of sensor devices is evident from the point that different IoT tion provided much higher capture capability at intermittent operation
devices such as the turbidity sensor help calculate the density of mi- (∼95%) for the microalgal strain Chlorella vulgaris than the maximum
croalgal biomass [118]. Experiments prove open raceway ponds to have CO2 capture efficiency in continuous operation (∼64%), which further
enhanced areal biomass productivity using carbonation column reac- abbreviated on varying the gas flow rate [130]. A second strategy to
tor (CCR), and the estimated cost seemed very low for the trials. The increment the capture efficiency in CRWP systems can be to increase
team also proposed a novel electropreciflocculation (ePF) reactor and the raceway length which help increase the residence time and hence
filter press module to increase biomass productivity efficiency for Nan- the efficiency. This help maintain the continuous supply of CO2 in the
nochloropsis salina to around 98.24%. CO2 capture remained within a process.
very economical range of 45.38–208.12 tons ha−1 y−1 , with the average The photobioreactors (PBRs) can be thought to be a closed complex
hovering around 95.39 tons ha−1 y−1 [119]. Generally, the experiments loop of biorefinery in itself, where all the necessary raw materials are
are conducted in a photo-heterotrophic mode with acetic acid or em- converted directly to the economically viable product in a single reactor
ploying a photo-autotrophic with CO2. A mixotrophic mode of operation optimally. In addition to proper and increased control over cultivation
reveals that microalgal species tend to achieve higher biomass produc- parameters and high biomass productivity, there are reduced chances of
tivity and a faster growth rate. C. vulgaris grows well under certain levels evaporation and contamination [131]. PBR configuration is an impor-
of CO2 concentrations using the photoautotrophic mode of cultivation, tant parameter to gage the biomass productivity and the capacity of mi-
it also grows fast, and provides a better CO2 [120]. Yu et al. improvised croalgae to remove pollutants. Additionally, the PBR diameter is a crit-
the system allowing for 5% CO2 [121]. The conditions stabled the pH ical design element for microalgae activity. How the surface-to-volume
at around 7 based on NaCO3 -CO2 and acetic acid-sodium acetate buffer ratio impacts light penetration is a predominant factor defining the PBR
respectively. That the activity of carbonic anhydrase and Rubisco was configuration [132]. Modifications made recently have been found to
inhibited, which was confirmed by the transcriptome sequencing analy- majorly influence light utilization, adequate mixing of nutrients, and
sis and enzymatic activity assay attributed to the better performance of better temperature control. The agitation system deserves special men-
this mode of operation. Suriya Narayan et al. studied the efficiency of tion, because of the operational stability it has brought in over years in
a novel algal species Coelastrella sp. FI69 [122,123], although very low algal cultivation in a closed system. The extent of light intensity and dis-
in percentage. This family of species has been found to possess diverse tribution is an important factor in deciding biomass productivity. The
traits with some of the major being its thermally tolerant nature and combination of light-harvesting capacity and light absorbance affects
higher biomass productivity [124]. In line with properties and expected PBR efficiency to a great extent [133]. Different microalgal species can
algal species’ properties, it adapted quickly to the exhaust conditions adapt themselves to the fluctuations in light intensity, which is impor-
and attained the highest biomass productivity, but there was scope for tant to prevent photodamage by accepting just the optimum amount of

9
S. Paul, S. Bera, R. Dasgupta et al. Energy Nexus 4 (2021) 100032

Table 3
Summary of the ORP systems- the highest biomass productivities and CO2 fixation rate attained during a system.

System description Target of the study Algal species Maximum biomass CO2 fixation rate Ref.
productivity

Semi-continuous mode with FG Dependence on the mode of Chlorella vulgaris 0.428±0.12 g L−1 102.66±5.77 mg L−1 d−1 [121]
operation and effect of FG
Semi-automated integrated with Protocol for carbon capture from Chlorella sorokiniana 0.385 g L−1 – [125]
power plant a power plant with FG
CO2 supplementation using CCR Process to mass produce native Nannochloropsis salina 7.5 to 34.4 g m−2 d−1 95.39 tons ha−1 y−1 (average) [121]
marine algal strain
−1 −1 −1 −1
CO2 and acetic acid added Testing mixotrophic cultivation Chlorella vulgaris 0.237 g L d 0.294 g L d [122]
alternatively strategy
LPG burner exhaust gas Check efficiency of novel algal Coelastrella sp. FI69 0.116 g L−1 d−1 0.202 g L−1 d−1 [122][123]
species for CO2 sequestration.
Diesel-fueled heating boiler Evaluating CO2 mass transfer Scenedesmus sp. 17 g m−2 day−1 – [126]

Table 4
A comparative analysis of the different PBR systems in use for microalgae cultivation for carbon capture.

Reactor type Characteristics and advantages Drawbacks Schematic

Tubular type • High surface area and volumetric biomass density • High concentration imbalance throughout the system Figs. 7 and 8
• Usually uses transparent tubes to allow for illumination • Reactor clean up problematic
• More energy demands • Accumulation of oxygen-detrimental to biomass growth
• Are typically of two types-vertical and horizontal
• CO2 residence time is high in horizontal reactor

Bubble column type • Possess higher CO2 conversion rate • Difficult scaling up Fig. 9
• Good mixing efficiency, thus having good gas exchange • High initial investment and maintenance cost
• Good light penetration

Airlift type • High mass transfer rate • Needs higher photosynthetic rates
• Good mixing available between phases with bare • Care to be taken so that there is no shear damage to cells
minimum shear stress due to aeration
• Low energy requirement

Flat plate • Large surface area to volume ratio • High hydrodynamic stress Fig. 10
• O2 accumulation minimum with available shortest path • Shear damage to cells rampant
• Exceptionally low power consumption • Imperfect gas mixing
• Low risk of culture contamination • Production of biomass per unit space is tentatively low
• Clean up difficult

Hybrid • Better control over process metrics • Requires control over hydrodynamic properties
• Increased productivity
• Low cost
• Low energy consumption

light to be utilized [134]. Longer exposures to higher light intensity can Presently, developed bioreactors have moved on from traditional de-
cause photoinhibition, thus saturation light intensity is to be maintained sign to novel integrated systems for higher carbon dioxide fixation effi-
in PBR systems. The pH of the medium needs careful calibration with ciencies and biomass productivity. Innovative designs are now emerging
algae showing the highest productivity in the range of 7–9, with some over the need for more varied environmental conditions and require-
showing growth capabilities in basic and acidic pH too. Modifications to ments.
the pH level could potentially change the physiochemical characteris- Senatore and his team developed a novel self-forming dynamic mem-
tics of cells such as their polarity or their biochemical properties [135]. brane integrated photobioreactor (MPBR), aimed at majorly increasing
Temperature is the rate-determining parameter of biomass productiv- biomass productivity and carbon capture from wastewater treatment
ity and CO2 fixation rate in PBR configuration. The optimum tempera- plants. They aimed at understanding the effect of operating principles
ture range is 15–300 Celsius, but there have many different correlations such as photosynthetic photon flux densities (PPFD), and the liquid/gas
found with the amount of lipid production from biomass and the un- ratio (L/G ratio), and incoming CO2 concentration. The biomass pro-
saturated fatty acid concentrations in the medium. The speed of algal ductivity reached a high of 1.01 g L−1 and the carbon capture removal
growth is also affected under natural temperature conditions. Lipid pro- efficiency a high of 80% at a PPFD of 120 μmol m−2 s−1 with an L/G ra-
duction is supported at a temperature range of about 25–300 Celsius, tio of 15, both of which were the highest that was tested in the category
but the amount of unsaturated fatty acid is seen to reduce with temper- [142].
ature, which is also the case with fixation efficiency and PBR produc- Several studies have compared the traditional existing PBRs with
tivity [136]. Studies at lower temperatures found decreased photosyn- new designs such as glass bottle PBRs, which seems to provide better
thetic rates and chlorophyll content, whereas temperature fluctuations working conditions required at high reactor volumes. It is important
affected the metabolism of cells greatly even in the acceptable range given the disadvantages of dealing with concentration imbalances in
[137]. high volumes of tubular PBRs, and the ease of using glass flask PBRs
Fundamental PBR designs have centered around the tubular-type, in its place. However, glass flask PBRs provide better results neither at
airlift, bubble column, and plate type designs. A summary table has been 0.04% nor 10% (v/v) CO2 flow rate. CO2 flow rate additionally, has also
provided to have a clear knowledge about traditional photobioreactor been found to be an important parameter for growth rate and biomass
systems (Table 4). productivity with certain studies limiting the amount of around 5% v/v.

10
S. Paul, S. Bera, R. Dasgupta et al. Energy Nexus 4 (2021) 100032

But, most importantly this study by Aghaalipour et al. has found stable Dunaliella salina, it was found to be growth-inhibiting, and additionally,
growth conditions for all studies of algal species, namely Scenedesmus the CO2 fixation rate also decreased, thus keeping 6% CO2 as the op-
obliquus, Monoraphidium contortum, Psammothidium sp, and Chlorella vul- timized flow rate. The study also concluded that oxygen, if present in
garis at 10% v/v carbon dioxide [143]. The PBR systems found increas- gas inhibits algal growth, and there can be nearly a 2.7-fold increase in
ing inorganic carbon concentration at higher CO2 concentrations, which productivity even at higher CO2 concentrations [152]. But it was better
was responsible for increased sources of carbon in the system, leading than its contemporary Nannochloropsis salina [153]. Table 5 presents the
to increased bioremediation [144]. Even, inorganic concentrations were advances in novel designs in PBR systms recently being developed for
found to be higher in vertical PBRs rather than in glass bottle reactors. different microalgal species.
But, the higher efficiency of vertical tubular PBRs over glass flask coun- Innovative PBR systems, such as air-lift flat-tube PBRs have been
terparts was simply due to its lower diameter and hence volume, which incorporated with airfoil-shaped deflectors and tested for different hy-
aided in better mixing, and efficient mass transfer. drodynamic properties. It was found to increase the time of microalgae
PBR systems in many cases have been studied in series with each suspension for better light accessibility. The biomass productivity and
other. The growth pattern although remains typically the same, the additionally the CO2 fixation rate found around 18.3% and 10.9% en-
biomass productivity continuously reduces over the PBRs. This was at- hancement due to the developed hydrodynamic condition [155]. 3-D
tributed to the reduction in CO2 concentration, which inherently in- tangential swirl plate (TTSP) PBR is seen to increase the turbulence in
hibited microalgae biomass growth. But, PBRs in series provided bet- the system, which ultimately leads to an increase of microalgae CO2
ter fixation efficiency than a single PBR control system. The study con- fixation rate by 30% in the study conducted [156]. Microbubble-driven
cluded that an optimum number of sequential-flow batch PBR (SFB-PBR) PBRs (MDPBR) found increased cell growth rate by careful optimization
systems was required to maintain efficient CO2 concentration over the of bubble size, which increased the mass transfer [157]. Azhand et al.
bioreactor systems in series. Also, the accumulation of dissolved oxy- found that compared to the internal sparger system, external sparger
gen should be kept noticed, for it can inhibit microalgae productivity had higher efficiency, but it was dependent on the cross-sectional area
[145]. Studies also directed at using Recirculating Media PBR (RMPBR) of the riser and downcomer, and a strong correlation exists between
which could increase CO2 capture without inhibiting microalgal growth, these parameters and the capture efficiency. The effect was more ev-
which was made by optimizing the hydrodynamic condition of recir- ident in the transient and heterogeneous flow regimes, where the gas
culating CO2 stream at a fixed concentration (in this case 5%) [146]. flow rate using external sparger was more than its counterpart due to
This led to decreased damage to the microalgal cells thus co-optimizing more cross-section area for the same superficial gas velocity [158]. The
both capture and productivity. The fundamental concept of two-phase input superficial gas velocity already plays a major role in understand-
mass transfer helps develop high-rate in-line carbonation for increased ing various hydrodynamic and conclusive parameters in CO2 capture
productivity. Jin et al. tested a few different microalgal cells with high systems in PBRs, and therefore, the dependence is very important and
carbon dioxide (v/v) % in the air, for growth of most microalgal cells requires intricate study (Fig. 11).
gets inhibited at around 5% CO2 in the flue gas. Therefore, for higher Many recent works have focused on devising novel PBR systems us-
capture efficiency from flue gas in industries, microalgal cells should be ing CFD simulation study, which predict the hydrodynamic properties
able to tolerate higher volumes of carbon dioxide, without compromis- and aeration rate optimally, and has been found quite successful. Hexag-
ing biomass productivity. The microalgal strain of Heynigia riparia SX01 onal airlift flat plate (HAFP) PBRs using CFD simulation proved to have
had the highest tolerance towards a high-volume flow rate of CO2 and better biomass productivity, with that being as high as 61%. Addition-
can seem unaffected, with high biomass productivity at 15% CO2 con- ally, the CO2 fixation and removal rate increased by nearly 80% and
centration in the ambient airflow. It was also supportive of the result 90% respectively, and thus can be tested at a pilot scale with proper flue
of the BLAST analysis which showed 18S rRNA sequences had a high gas incorporation [159]. Other studies involving CFD simulation were
identity in H. riparia CCAP 222/47 (100%) [147]. around understanding the flow field which could be optimized using
Studies, additionally signify the difference in biomass productivity double paddlewheels in a flat plate photoreactor. There was increased
and carbon capture efficiency under formulated flue gas and real flue agitation and the double paddlewheel intensified the flow of microal-
gas. The studies concluded that the differences in conclusions can be ex- gal solution, which was proposed to be the cause of better microalgal
plained by the actual CO2 concentration, and the feeding period, in addi- biomass growth. The study was targeted at understanding the flashlight
tion to how both react to external factors like SO2 and NOx that also tend effect and the intensified flow field consequently enhancing the flash
to be present [148]. Unfiltered flue gas requires microalgal species to cycle efficiency [160].
slowly adapt over time, because of the sudden drop of pH in the medium
with the sudden influx of SOX and NOX . Focus can also be shifted to 6. The energy-water-food (EWF) nexus using microalgae biomass
having a mixed microalgal consortia, which can help in increased dom-
inance. A study also shows that Desmodesmus spp. is the most dominant With algae biomass produced and used for varied purposes such as
step, among other brackish and freshwater cultures [149]. The same the production of biofuels, a more carbon-neutral or at times carbon-
team also found out that microalgae in PBRs were also viable for heavy negative approach to CCS has been bioenergy based on the biomass and
metal capture from flue gases which contained a high amount of heavy then storage of the captured carbon, termed Bio-Energy based on Car-
metals and alternatively provide quantitative biomass amount [150]. bon Capture and Storage (BECCS). BECCS, also can produce value-added
More than the original species, extractable mutants can be more chemical products like methanol and urea [161]. It is touted as the car-
thermo-tolerant and CO2 tolerant than the original one and are easily ex- bon negative approach, for its apparent end being the captured CO2
tractable by NTG (N-methyl-N′-nitro-N-nitrosoguanidine) mutagenesis stored underground in geological storage. In addition to the production
[151]. The mutants also had increased tolerance to SOx and NOx gases of multiple value-added products, this utilization approach can invari-
which are generally sequestered much less than carbon dioxide, whereas ably process up to 3.7 Gt of CO2 emissions each year, a value equivalent
alternatively they can be used for growth and increased biomass produc- to nearly 10% of the global carbon emissions [162]. The EWF nexus with
tivity. But the excess presence of gases like SO2 can cause high growth this microalgae biomass and further products helps scientists around the
inhibition due to a decrease in pH. NO hydrolysis can also cause a re- world understand the connections between these systems and the food
duction in pH as direct consumption of NO by the algal cells is difficult. system scenario [163]. Most analysis within the EWF nexus has been fo-
In conclusion, the outdoor mode of PBR growth provided high biomass cused on managing resource efficiency and alternatively environmental
productivity and carbon capture efficiency than an indoor mode of cul- emissions, which is typically non-existent [164]. BECCS coupled with
ture. Chen et al. also tried replicating real-time flue gas composition by the capacity for agricultural greenhouse enrichment understands the
increasing the CO2 concentration from 6% to 20%, but for the case of process model, supply chains, and geospatial analysis, and hence en-

11
S. Paul, S. Bera, R. Dasgupta et al. Energy Nexus 4 (2021) 100032

Table 5
Summary of the recent studies undertaken for microalgae assisted carbon capture with novel PBR systems.

Bioreactor type Microalgae species Biomass productivity∗ CO2 fixation rate∗ Carbon source Ref.
−1
MPBR Chlorella Vulgaris 1.01 g L – Conveyed flows [142]
Vertical Tubular Monoraphidium contortum 0.26 g L−1 D−1 1.4 g CO2 L−1 D−1 Specially prepared (similar to [142]
PBR Psammothidium sp 0.75 g L−1 D−1 3.23 g CO2 L−1 D−1 powerplant flue gas
Chlorella vulgaris 0.61 g L−1 D−1 3.35 g CO2 L−1 D−1 compositions)
Scenedesmus obliquus 0.45 g L−1 D−1 2.4 g CO2 L−1 D−1
SFB-PBR Chlorella vulgaris 0.83–0.86 g L−1 D−1 – Normal air but at different air [145]
flow rate
−1 −1 −1 −1
RM-PBR Chlorella vulgaris 0.0321 g L D 0.04566 g CO2 L D Recirculated 5% CO2 [146]
Bubble column PBR Chlorella 0.18±0.02 g L−1 D−1 0.34±0.01 g CO2 L−1 D−1 Filtered ambient air containing [147]
sorokiniana XJ02 0.03%, 5%, 10% and 15% (v/v)
Chlorella sorokiniana GS03 0.36±0.01 g L−1 D−1 0.66±0.01 g CO2 L−1 D−1 of CO2 .
Chlorella sp. NM01 0.22±0.01 g L−1 D−1 0.35±0.01 g CO2 L−1 D−1
Heynigia riparia SX01 0.39±0.01 g L−1 D−1 0.46±0.02 g CO2 L−1 D−1
Desmodesmus communis 0.20±0.03 g L−1 D−1 0.37±0.01 g CO2 L−1 D−1
GS05
Scenedesmus obliquus NM02 0.13±0.02 g L−1 D−1 0.24±0.02 g CO2 L−1 D−1
Hybrid Bubble Scenedesmus obtusiusculus 0.0690 g L−1 D−1 160.7 g CO2 L−1 D−1 Formulated flue gas [148]
column PBR AT-UAM 0.0418 g L−1 D−1 0.1114 g CO2 L−1 D−1 Real flue gas
Outdoor PBR Chlorella vulgaris ESP-31 (mutant 283) 0.24315±0.07 g L−1 D−1 0.45713±0.13305 g CO2 L−1 D−1 Simulated flue gas with 25% CO2 [151]
PBR Botryococcus braunii – 0.532 g CO2 L−1 D−1 20% CO2 mixed with N2 . [154]
Scenedesmus sp. – 2177 g CO2 L−1 D−1

All data provided are the highest reported data mentioned in literature.

Fig. 11. The effect of input superficial gas


velocity on (a) the specific growth rate over
the whole culture time, (b) cell concentra-
tion over culture time, (c) CO2 removal ef-
ficiency, and (d) downcomer liquid circula-
tion time and riser superficial liquid velocity
[156]. (Reprinted with permission, Elsevier).

forces the synergy between EWF nexus and BECCS [165]. Since thermo- availability and water supply, instead of influencing the water demand
electric power generation has multiple issues in the Energy-Water-CO2 much [169]. Enhancing agricultural productivity using CO2 fertilization
nexus, technological alternatives have been proposed for carbon seques- can also be a part of the prescribed model [170]. It has been seen that
tration and air quality regulation, but it turns out that some of the pro- BECCS sustainability depends profoundly on CO2 removal targets set,
posed methods although environmentally sustainable, is economically and the choice and constrained number of resources available-an inter-
expensive. Water concerns are also a major issue in power plants affect- esting parameter that defines CCS [171]. The potential trade-offs be-
ing the water-energy nexus adversely [166]. The use of sophisticated tween resource efficiency, environmental philanthropy, and technical
economic models using robust economic analysis should help identify and economic performance needs proper design of BECCS value chain
the potential trade-offs between economic and environmental tradeoffs and policy decisions [172]. Additionally, its prospect depends on the ul-
[167]. This is evident when studies suggest that Carbon Capture as a timate use of the carbon captured. The convenience of BECCS depends
greenhouse gas mitigation strategy increases water stress, because of on the distance and how captured carbon is delivered to a potential end-
its high process water requirement [168]. But the continuous release user. The commercial prospect and viability of a BECCS plant therefore
of CO2 that can result in degrading climate change, affects the water finally depends on a fully-operational plant, which can answer the cer-

12
S. Paul, S. Bera, R. Dasgupta et al. Energy Nexus 4 (2021) 100032

tain constraints EWF nexus assessment studies face [173]. Therefore, the needs to be brought in for proper commercial use. The water source also
study of this nexus is important in Eco-Industrial Parks (EIP), which is plays an important role in biomass production, and often as a limiting
motivated by increasing demand for sustainable development in waste factor in both open and closed systems.
integrated microalgal biorefinery. It is also run by the idea that collabo- Commercial startups have already started in many different coun-
ration between certain industries can increase profit bars. Fouladi et al. tries, with names ranging from AlgaEnergy, PhytoBloom-Microalgae by
proposed a superstructure and optimization formula to capture the syn- Necton, A4F-Algae for Future, ALGAE Biotechnologia, Neoalgae, Syn-
ergy between different sectors to develop a linkage between EWF nexus- oxis Algae, AlgoSource, and many others. For many, they are already
the economic and environmental trade-offs [174]. Alternatively, link- collaborating with industries and providing scalable solutions for reduc-
ages and interconnections also exist between globalization, economic ing carbon emissions. But there remains room for expansion. For future
growth, and carbon emissions, which is critical to fabricating future projections, after certain developments are made the cost of carbon cap-
sustainable development policies regarding carbon emissions [175]. It ture should be taken care of. The cost for carbon sequestration should
is, therefore, also important to understand the power generation tech- not increase to the high value given that in some cases, it might be purely
nology portfolios in association with such industries to assess the eco- out of environmental philanthropy without any economic incentive.
nomic risks and optimize the nexus [176]. Heavy emitting countries like
China require studying regional characteristics for reducing greenhouse Declaration of Competing Interest
gas emissions incorporating both renewable energy and CCS. Therefore,
their policy portfolios, besides incorporating trade-offs should optimize The authors declare that they have no conflict of interest.
design and operational decisions [177].
With CCU already a trending topic in international meets like COP26, Acknowledgment
interlinkages with EWF nexus are very important parameters and need
rigorous studies. It is also important for the holistic development of This work was supported by Science and Engineering Research Board
CCUS routes, which can extend beyond its sectoral proved applications (SERB) grants funded by Department of Science and Technology (DST)
[178,179]. A viability study for post-combustion capture plants con- Central, Government of India through Teachers Associateship for Re-
cluded that sharp trade-offs in the water, energy, and carbon nexus, and search Excellence (TAR/2018/000195) (S. Roy). Author would also like
therefore any policy decision by governments should depend on all the to acknowledge Department of Science and Technology (DST), Min-
complex processes involved [180]. Studies even conclude that amine in- istry of Science and Technology, Government of India funded project
tegrated CC systems are not very water-intensive if the base power plant under the MI IC#5′ Conversion of Sunlight to Storable fuels’ issued
is efficient enough [181]. Some also studied the performance of poly- by DBT-DST Joint Funding Opportunity, Central Government of In-
mers in carbon capture [182]. Even from the multitude of products that dia through Mission Innovation Programme DST(DST/TMD(EWO)/IC5-
can be produced from CCU method, methanol, which often describes 2018/06, dated 15.11.2019) (S. Roy), for providing financial support.
itself as a greener alternative as power and transportation fuel, is not
Reference
the better option when it comes to decarbonizing the electricity vectors.
Instead using renewable energy sources and direct carbon capture offer [1] J. Houghton, Global warming, Rep. Prog. Phys. 68 (2005) 1343–1403.
greater environmental benefits, with no major bottlenecks in economic [2] B. Raj, O. Singh, Study of impacts of global warming on climate change: rise in sea
parameters [183]. Various studies investigate integrated algae cultiva- level and disaster frequency, Global Warming - Impacts and Future Perspectives,
InTech, 2012.
tion in processes like waste heat recovery from microturbine in seawater [3] C.K. Chanda, D. Bose, Challenges of employing renewable energy for reducing
desalinization, with encouraging results both on the economic and en- greenhouse gases (GHGs) and carbon footprint, in: Encyclopedia of Renewable and
vironmental forefront [184]. Sustainable Materials, Elsevier, 2020, pp. 346–365.
[4] J. Goldemberg, Energy choices toward a sustainable future, Environment 49 (2007)
7–17.
7. Future outlook and conclusive remarks [5] Global Energy Review: CO2 Emissions in 2020, International Energy Agency -IEA,
Paris, 2021.
[6] C. Song, W. Pan, S.T. Srimat, J. Zheng, Y. Li, Y.-H. Wang, B.-Q. Xu, Q.-M. Zhu,
It is worthwhile to note that as researcher target for more species to Tri-reforming of methane over Ni catalysts for CO2 conversion to syngas with de-
be tested, cultivated, and commercialized for carbon sequestration, they sired H2/CO ratios using flue gas of power plants without CO2 separation, in: car-
have to take the potential impact of the climate change happening over bon dioxide utilization for global sustainability, in: Proceedings of 7ththe Interna-
tional Conference on Carbon Dioxide Utilization, Elsevier, 2004, pp. 315–322.
the years, and how they affect algae- both microalgae and macroalgae
[7] P. Williamson, S. Widdicombe, The rise of CO 2 and ocean acidification, in: Ency-
growth. Because, the consequence of climate change has already started clopedia of the Anthropocene, Elsevier, 2018, pp. 51–59.
to affect biodiversity and ecosystems gravely, and studies need to be [8] F. Nocito, A. Dibenedetto, Atmospheric CO2 mitigation technologies: carbon cap-
conducted under more severe conditions. As studies are undertaken, ture utilization and storage, Curr. Opin. Green Sustain. Chem. 21 (2020) 34–43.
[9] L. Zhu, X. Yao, X. Zhang, Evaluation of cooperative mitigation: captured carbon
temperature fluctuations from place to place should be kept in mind, dioxide for enhanced oil recovery, Mitig. Adapt. Strateg. Glob. Change 25 (2020)
as a highly successful carbon-sequestering algal species in the hot and 1261–1285.
humid temperature zones might lose its efficiency in a cold and arid cli- [10] E. Adu, Y. Zhang, D. Liu, Current situation of carbon dioxide capture, storage, and
enhanced oil recovery in the oil and gas industry, Can. J. Chem. Eng. 97 (2019)
mate. The majority of the studies are done with either air flowing inside 1048–1076.
simulated near to those of real industrial flue gases. But there are very [11] E.G. Hertwich, M. Aaberg, B. Singh, A.H. Strømman, Life-cycle assessment of car-
few studies that actually incorporate flue gas from industries, and there- bon dioxide capture for enhanced oil recovery, Chin. J. Chem. Eng. 16 (2008)
343–353.
fore future studies should aim more towards understanding the effect of [12] E. Koohestanian, J. Sadeghi, D. Mohebbi-Kalhori, F. Shahraki, A. Samimi, A novel
industrial flue gas which might have more either growth accelerating process for CO2 capture from the flue gases to produce urea and ammonia, Energy
or growth-inhibiting components, The CCM strategy might be an im- 144 (2018) 279–285.
[13] W.N.R. Wan Isahak, Z.A. Che Ramli, M.W. Mohamed Hisham, M.A. Yarmo, The
portant tool to mitigate the carbon emission problems. Although there
formation of a series of carbonates from carbon dioxide: capturing and utilisation,
is an urgent need to act, studies should deeply study the life-cycle as- Renew. Sustain. Energy Rev. 47 (2015) 93–106.
sessments and understand all environmental, social, and economic im- [14] M. Liu, G. Gadikota, Single-step, low temperature and integrated CO2 capture and
conversion using sodium glycinate to produce calcium carbonate, Fuel 275 (2020)
pacts of the study in progress. Secondly, the selection of algal strain
117887.
and its optimum method of carbon fixation is of umpteen importance. [15] D. Bellotti, M. Rivarolo, L. Magistri, A.F. Massardo, Feasibility study of methanol
Biological characteristics and cultivation strategies can be different for production plant from hydrogen and captured carbon dioxide, J. CO2 Util. 21
different species and should be tested before application in commercial (2017) 132–138.
[16] G. Leonzio, P.U. Foscolo, E. Zondervan, I.D.L. Bogle, Scenario Analysis of Carbon
usage. This arises due to the interconnection of the different subjects in Capture, Utilization (Particularly Producing Methane and Methanol), and Storage
the study of CO2 sequestration, and therefore a proper interconnection (CCUS) Systems, Ind. Eng. Chem. Res. 59 (2020) 6961–6976.

13
S. Paul, S. Bera, R. Dasgupta et al. Energy Nexus 4 (2021) 100032

[17] G.A. Olah, A. Goeppert, G.K.S. Prakash, Chemical recycling of carbon dioxide to N.T. Lan Chi, P.A. Duc, A. Pugazhendhi, A review on prospective production of
methanol and dimethyl ether: from greenhouse gas to renewable, environmentally biofuel from microalgae, Biotechnol. Rep. 27 (2020) e00509.
carbon neutral fuels and synthetic hydrocarbons, J. Org. Chem. 74 (2008) 487–498. [49] C. Debnath, T.K. Bandyopadhyay, B. Bhunia, U. Mishra, S. Narayanasamy,
[18] S. Michailos, S. McCord, V. Sick, G. Stokes, P. Styring, Dimethyl ether synthesis via M. Muthuraj, Microalgae: Sustainable resource of carbohydrates in third-genera-
captured CO2 hydrogenation within the power to liquids concept: A techno-eco- tion biofuel production, Renew. Sustain. Energy Rev. 150 (2021) 111464.
nomic assessment, Energy Convers. Manage. 184 (2019) 262–276. [50] Sk.A. Moyez, S. Roy, Dual-step thermal engineering technique: A new approach for
[19] S.S. Iyer, I. Bajaj, P. Balasubramanian, M.M.F. Hasan, Integrated carbon capture fabrication of efficient CH3 NH3 PbI3 -based perovskite solar cell in open air condi-
and conversion to produce syngas: novel process design, intensification, and opti- tion, Sol. Energy Mater. Sol. Cells 185 (2018) 145.
mization, Ind. Eng. Chem. Res. 56 (2017) 8622–8648. [51] A. Aliyu, J.G.M. Lee, A.P. Harvey, Microalgae for biofuels: A review of thermochem-
[20] S. Bera, D. Sengupta, S. Roy, K. Mukherjee, Research into dye-sensitized solar cells: ical conversion processes and associated opportunities and challenges, Bioresour.
a review highlighting progress in India, J. Phys. Energy 3 (2021) 032013. Technol. Rep. 15 (2021) 100694.
[21] J. Skocek, M. Zajac, M. Ben Haha, Carbon Capture and Utilization by mineralization [52] D.F. Lozano-Garcia, S.P. Cuellar-Bermudez, E. del Rio-Hinojosa, F. Betancourt,
of cement pastes derived from recycled concrete, Sci. Rep. 10 (2020). G.S. Aleman-Nava, R. Parra-Saldivar, Potential land microalgae cultivation in Mex-
[22] T.D. Moshood, G. Nawanir, F. Mahmud, Microalgae biofuels production: A system- ico: From food production to biofuels, Algal Res. 39 (2019) 101459.
atic review on socioeconomic prospects of microalgae biofuels and policy implica- [53] B.C. Klein, M.F. Chagas, M.D.B. Watanabe, A. Bonomi, R. Maciel Filho, Low carbon
tions, Environ. Chall. 5 (2021) 100207. biofuels and the New Brazilian National Biofuel Policy (RenovaBio): A case study
[23] A. Melis, Solar energy conversion efficiencies in photosynthesis: Minimizing the for sugarcane mills and integrated sugarcane-microalgae biorefineries, Renew. Sus-
chlorophyll antennae to maximize efficiency, Plant Sci. 177 (2009) 272–280. tain. Energy Rev. 115 (2019) 109365.
[24] K.M. Weyer, D.R. Bush, A. Darzins, B.D. Willson, Theoretical Maximum Algal Oil [54] M. Ravanipour, A. Hamidi, A.H. Mahvi, Microalgae biodiesel: A systematic review
Production, Bioenerg. Res. 3 (2009) 204–213. in Iran, Renew. Sustain. Energy Rev. 150 (2021) 111426.
[25] H. Vieira de Mendonça, P. Assemany, M. Abreu, E. Couto, A.M. Maciel, R.L. Duarte, [55] N. Hossain, M.H. Hasan, T.M.I. Mahlia, A.H. Shamsuddin, A.S. Silitonga, Feasibil-
M.G. Barbosa dos Santos, A. Reis, Microalgae in a global world: New solutions for ity of microalgae as feedstock for alternative fuel in Malaysia: a review, Energy
old problems? Renew. Energy 165 (2021) 842–862. Strategy Rev. 32 (2020) 100536.
[26] C. Wiencke, M.N. Clayton, I. Gómez, K. Iken, U.H. Lüder, C.D. Amsler, U. Karsten, [56] IPCC, Summary for Policymakers, in: V. MassonDelmotte, P. Zhai, A. Pirani,
D. Hanelt, K. Bischof, K. Dunton, Life strategy, ecophysiology and ecology of sea- S.L. Connors, C. Péan, S. Berger, N. Caud, Y. Chen, L. Goldfarb, M.I. Gomis,
weeds in polar waters, Rev. Environ. Sci. Biotechnol. 6 (2006) 95–126. M. Huang, K. Leitzell, E. Lonnoy, J.B.R. Matthews, T.K. Maycock, T. Waterfield,
[27] M.H. Spalding, Microalgal carbon-dioxide-concentrating mechanisms: chlamy- O. Yelekçi, R. Yu, B. Zhou (Eds.)Climate Change 2021: The Physical Science Basis.
domonas inorganic carbon transporters, J. Exp. Bot. 59 (2007) 1463–1473. Contribution of Working Group I to the Sixth Assessment Report of the Intergov-
[28] C. Jansson, T. Northen, Calcifying cyanobacteria—the potential of biomineraliza- ernmental Panel On Climate Change, Cambridge University Press, 2021 In Press.
tion for carbon capture and storage, Curr. Opin. Biotechnol. 21 (2010) 365–371. [57] B. Behera, N. Aly, P. Balasubramanian, Biophysical model and techno-economic
[29] P. Spolaore, C. Joannis-Cassan, E. Duran, A. Isambert, Commercial applications of assessment of carbon sequestration by microalgal ponds in Indian coal based power
microalgae, J. Biosci. Bioeng. 101 (2006) 87–96. plants, J. Clean. Prod. 221 (2019) 587–597.
[30] J.J. Milledge, Commercial application of microalgae other than as biofuels: a brief [58] L. Ou, S. Banerjee, H. Xu, A.M. Coleman, H. Cai, U. Lee, M.S. Wigmosta, T. Hawkins,
review, Rev. Environ. Sci. Biotechnol. 10 (2010) 31–41. Utilizing high-purity carbon dioxide sources for algae cultivation and biofuel pro-
[31] S.A. Razzak, M.M. Hossain, R.A. Lucky, A.S. Bassi, H. de Lasa, Integrated CO2 cap- duction in the United States: opportunities and challenges, J. Clean. Prod. (2021)
ture, wastewater treatment and biofuel production by microalgae culturing—A re- 128779.
view, Renew. Sustain. Energy Rev. 27 (2013) 622–653. [59] J. Fu, Y. Huang, Q. Liao, A. Xia, Q. Fu, X. Zhu, Photo-bioreactor design for microal-
[32] H.M. Singh, R. Kothari, R. Gupta, V.V. Tyagi, Bio-fixation of flue gas from thermal gae: a review from the aspect of CO2 transfer and conversion, Bioresour. Technol.
power plants with algal biomass: Overview and research perspectives, J. Environ. 292 (2019) 121947.
Manage. 245 (2019) 519–539. [60] J.C.M. Pires, M.C.M. Alvim-Ferraz, F.G. Martins, Photobioreactor design for mi-
[33] V. Bhola, F. Swalaha, R. Ranjith Kumar, M. Singh, F. Bux, Overview of the poten- croalgae production through computational fluid dynamics: A review, Renew. Sus-
tial of microalgae for CO2 sequestration, Int. J. Environ. Sci. Technol. 11 (2014) tain. Energy Rev. 79 (2017) 248–254.
2103–2118. [61] J. Assunção, F.X. Malcata, Enclosed “non-conventional” photobioreactors for mi-
[34] W. Klinthong, Y.-H. Yang, C.-H. Huang, C.-S. Tan, A review: microalgae and their croalga production: a review, Algal Res. 52 (2020) 102107.
applications in CO2 capture and renewable energy, Aerosol Air Qual. Res. 15 (2015) [62] G.G. Zaimes, V. Khanna, Microalgal biomass production pathways: evaluation of
712–742. life cycle environmental impacts, Biotechnol. Biofuels 6 (2013) 88.
[35] J. Singh, D.W. Dhar, Overview of Carbon Capture Technology: Microalgal Biore- [63] T.F. Wall, Combustion processes for carbon capture, Proc. Combust. Inst. 31 (2007)
finery Concept and State-of-the-Art, Front. Mar. Sci. 6 (2019). 31–47.
[36] D. Narita, Economic optimality of CCS use: a resource-economic model, SSRN J. [64] A. Mukhtar, S. Saqib, N.B. Mellon, M. Babar, S. Rafiq, S. Ullah, M.A. Bustam,
(2009). A.G. Al-Sehemi, N. Muhammad, M. Chawla, CO2 capturing, thermo-kinetic princi-
[37] J. Cheng, Y. Zhu, Z. Zhang, W. Yang, Modification and improvement of microalgae ples, synthesis and amine functionalization of covalent organic polymers for CO2
strains for strengthening CO2 fixation from coal-fired flue gas in power plants, separation from natural gas: A review, J. Nat. Gas Sci. Eng. 77 (2020) 103203.
Bioresour. Technol. 291 (2019) 121850. [65] B.J.P. Buhre, L.K. Elliott, C.D. Sheng, R.P. Gupta, T.F. Wall, Oxy-fuel combustion
[38] W.-R. Lin, S.-I. Tan, C.-C. Hsiang, P.-K. Sung, I.-S. Ng, Challenges and opportu- technology for coal-fired power generation, Prog. Energy Combust. Sci. 31 (2005)
nity of recent genome editing and multi-omics in cyanobacteria and microalgae 283–307.
for biorefinery, Bioresour. Technol. 291 (2019) 121932. [66] R. Verma, A. Srivastava, Carbon dioxide sequestration and its enhanced utilization
[39] K. Jothibasu, D.W. Dhar, S. Rakesh, Recent developments in microalgal genome by photoautotroph microalgae, Environ. Dev. 27 (2018) 95–106.
editing for enhancing lipid accumulation and biofuel recovery, Biomass Bioenergy [67] J. Singh, D.W. Dhar, Overview of carbon capture technology: microalgal biorefin-
150 (2021) 106093. ery concept and state-of-the-art, Front. Mar. Sci. 6 (2019).
[40] A. Brar, M. Kumar, T. Soni, V. Vivekanand, N. Pareek, Insights into the genetic [68] C.B. Field, Primary production of the biosphere: integrating terrestrial and oceanic
and metabolic engineering approaches to enhance the competence of microalgae components, Science 281 (1998) 237–240.
as biofuel resource: a review, Bioresour. Technol. 339 (2021) 125597. [69] E. Suali, R. Sarbatly, Conversion of microalgae to biofuel, Renew. Sustain. Energy
[41] B. Barati, K. Zeng, J. Baeyens, S. Wang, M. Addy, S.-Y. Gan, A. El-Fatah Abomohra, Rev. 16 (2012) 4316–4342.
Recent progress in genetically modified microalgae for enhanced carbon dioxide [70] H.J. Ryu, K.K. Oh, Y.S. Kim, Optimization of the influential factors for the improve-
sequestration, Biomass Bioenergy 145 (2021) 105927. ment of CO2 utilization efficiency and CO2 mass transfer rate, J. Ind. Eng. Chem.
[42] R. Kholssi, P.V. Ramos, E.A.N. Marks, O. Montero, C. Rad, 2Biotechnological uses of 15 (2009) 471–475.
microalgae: a review on the state of the art and challenges for the circular economy, [71] E. Suali, R. Sarbatly, Conversion of microalgae to biofuel, Renew. Sustain. Energy
Biocatal. Agric. Biotechnol. (2021) 102114. Rev. 16 (2012) 4316–4342.
[43] S.R. Chia, K.W. Chew, H.Y. Leong, S.-H. Ho, H.S.H. Munawaroh, P.L. Show, CO2 [72] B. Zhao, Y. Su, Macro assessment of microalgae-based CO2 sequestration: Environ-
mitigation and phycoremediation of industrial flue gas and wastewater via microal- mental and energy effects, Algal Res. 51 (2020) 102066.
gae-bacteria consortium: possibilities and challenges, Chem. Eng. J. 425 (2021) [73] Y. Gao, C. Gregor, Y. Liang, D. Tang, C. Tweed, Algae biodiesel - a feasibility report,
131436. Chem. Cent. J. 6 (2012).
[44] J. Arun, K.P. Gopinath, P. SundarRajan, V. Felix, M. JoselynMonica, R. Malolan, A [74] S. Fon Sing, A. Isdepsky, M.A. Borowitzka, N.R. Moheimani, Production of biofuels
conceptual review on microalgae biorefinery through thermochemical and biolog- from microalgae, Mitig. Adapt. Strateg. Glob. Change 18 (2011) 47–72.
ical pathways: Bio-circular approach on carbon capture and wastewater treatment, [75] F.G.A. Fernández, A. Reis, R.H. Wijffels, M. Barbosa, V. Verdelho, B. Llamas, The
Bioresour. Technol. Rep. 11 (2020) 100477. role of microalgae in the bioeconomy, New Biotechnol. 61 (2021) 99–107.
[45] L.-L. Zhuang, M. Li, H. Hao Ngo, Non-suspended microalgae cultivation for wastew- [76] H. Leflay, J. Pandhal, S. Brown, Direct measurements of CO2 capture are essential
ater refinery and biomass production, Bioresour. Technol. 308 (2020) 123320. to assess the technical and economic potential of algal-CCUS, J. CO2 Util. 52 (2021)
[46] J.C.M. Pires, M.C.M. Alvim-Ferraz, F.G. Martins, M. Simões, Carbon dioxide capture 101657.
from flue gases using microalgae: Engineering aspects and biorefinery concept, [77] I.K. Chung, J. Beardall, S. Mehta, D. Sahoo, S. Stojkovic, Using marine macroalgae
Renew. Sustain. Energy Rev. 16 (2012) 3043–3053. for carbon sequestration: a critical appraisal, J. Appl. Phycol. 23 (2010) 877–886.
[47] V. Ananthi, R. Raja, I.S. Carvalho, K. Brindhadevi, A. Pugazhendhi, A. Arun, A real- [78] D. Moreira, J.C.M. Pires, Atmospheric CO2 capture by algae: Negative carbon diox-
istic scenario on microalgae-based biodiesel production: Third generation biofuel, ide emission path, Bioresour. Technol. 215 (2016) 371–379.
Fuel 284 (2021) 118965. [79] L.M.L. Laurens, M. Lane, R.S. Nelson, Sustainable seaweed biotechnology solutions
[48] R. Ganesan, S. Manigandan, M.S. Samuel, R. Shanmuganathan, K. Brindhadevi, for carbon capture, composition, and deconstruction, Trend. Biotechnol. 38 (2020)
1232–1244.

14
S. Paul, S. Bera, R. Dasgupta et al. Energy Nexus 4 (2021) 100032

[80] D.A. Roberts, N.A. Paul, M.I. Bird, R. de Nys, Bioremediation for coal-fired power into the microalgae cultivation technology and harvesting process for biofuel pro-
stations using macroalgae, J. Environ. Manage. 153 (2015) 25–32. duction: A review, Renew. Sustain. Energy Rev. 115 (2019) 109361.
[81] J. Masojı´dek, M. Koblızek, G. Torzillo, Photosynthesis in microalgae, in: A. Rich- [114] A.B. Fulke, S.N. Mudliar, R. Yadav, A. Shekh, N. Srinivasan, R. Ramanan, K. Krish-
mond (Ed.), Handbook of Microalgal Culture: Biotechnology and Applied Phycol- namurthi, S.S. Devi, T. Chakrabarti, Bio-mitigation of CO2 , calcite formation and
ogy, Blackwell Science Ltd., Oxford, UK, 2004. simultaneous biodiesel precursors production using Chlorella sp, Bioresour. Tech-
[82] M. Ras, J.-P. Steyer, O. Bernard, Temperature effect on microalgae: a crucial factor nol. 101 (2010) 8473–8476.
for outdoor production, Rev. Environ. Sci. Biotechnol. 12 (2013) 153–164. [115] S. Li, S. Luo, R. Guo, Efficiency of CO2 fixation by microalgae in a closed raceway
[83] S.S. Oncel, A. Kose, D.S. Oncel, Carbon sequestration in microalgae photobioreac- pond, Bioresour. Technol. 136 (2013) 267–272.
tors building integrated, in: Start-Up Creation, Elsevier, 2020, pp. 161–200. [116] M. U., N. J. Mehar, A. Shekh, R. Sarada, V.S. Chauhan, S. Mudliar, Automation of
[84] M. Mondal, S. Khanra, O.N. Tiwari, K. Gayen, G.N. Halder, Role of carbonic anhy- pilot-scale open raceway pond: A case study of CO2 -fed pH control on Spirulina
drase on the way to biological carbon capture through microalgae-A mini review, biomass, protein and phycocyanin production, J. CO2 Util. 33 (2019) 384–393.
Environ. Prog. Sustain. Energy 35 (2016) 1605–1615. [117] G. Yadav, B.K. Dubey, R. Sen, A comparative life cycle assessment of microalgae
[85] D. Sültemeyer, Carbonic anhydrase in eukaryotic algae: characterization, regula- production by CO2 sequestration from flue gas in outdoor raceway ponds under
tion, and possible function during photosynthesis, Can. J. Bot. 76 (1998) 962–972. batch and semi-continuous regime, J. Clean. Prod. 258 (2020) 120703.
[86] J. Beardall, J.A. Raven, The potential effects of global climate change on microalgal [118] I. Hermadi, I.R. Setiadianto, D.F. Al Zahran, M.N. Simbolon, G. Saefurahman,
photosynthesis, growth and ecology, Phycologia 43 (2004) 26–40. D.S. Wibawa, Y. Arkeman, Development of smart algae pond system for microalgae
[87] L. Brennan, P. Owende, Biofuels from microalgae—A review of technologies for biomass production, IOP Conf. Ser.: Earth Environ. Sci. 749 (2021) 012068.
production, processing, and extractions of biofuels and co-products, Renew. Sus- [119] N. Mohan, P.H. Rao, A.B. Boopathy, R. Rengasamy, S. Chinnasamy, A sustainable
tain. Energy Rev. 14 (2) (2010) 557–577. process train for a marine microalga-mediated biomass production and CO2 cap-
[88] A.S. Mirón, M.C.C. Garcı́a, A.C. Gómez, F.G. Camacho, E.M. Grima, Y. Chisti, Shear ture: A pilot-scale cultivation of Nannochloropsis salina in open raceway ponds and
stress tolerance and biochemical characterization of Phaeodactylum tricornutum in harvesting through electropreciflocculation, Renew. Energy 173 (2021) 263–272.
quasi steady-state continuous culture in outdoor photobioreactors, Biochem. Eng. [120] X.-M. Shi, H.-J. Liu, X.-W. Zhang, F. Chen, Production of biomass and lutein by
J. 16 (2003) 287–297. Chlorella protothecoides at various glucose concentrations in heterotrophic cul-
[89] C.-H. Huang, C.-S. Tan, A Review: CO2 Utilization, Aerosol Air Qual. Res. 14 (2014) tures, Process Biochem. 34 (1999) 341–347.
480–499. [121] Q. Yu, H. Wang, X. Li, Y. Yin, S. Qin, B. Ge, Enhanced biomass and CO2 seques-
[90] J.T. Hauck, S.J. Scierka, M.B. Perry, Effects of simulated flue gas on growth of tration of Chlorella vulgaris using a new mixotrophic cultivation method, Process
microalgae, Am. Chem. Soc. Div. Polym. Chem. 41 (1996) 1391–1396. Biochem. 90 (2020) 168–176.
[91] B. Zhao, Y. Su, Process effect of microalgal-carbon dioxide fixation and biomass [122] G. Suriya Narayanan, G. Kumar, S. Seepana, R. Elankovan, M. Premalatha, Utiliza-
production: A review, Renew. Sustain. Energy Rev. 31 (2014) 121–132. tion of unfiltered LPG-burner exhaust-gas emission using microalga Coelastrella sp,
[92] S.-Y. Chiu, C.-Y. Kao, T.-T. Huang, C.-J. Lin, S.-C. Ong, C.-D. Chen, J.-S. Chang, J. CO2 Util. 29 (2019) 283–295.
C.-S. Lin, Microalgal biomass production and on-site bioremediation of carbon diox- [123] Acute Exposure Guideline Levels for Selected Airborne Chemicals, National
ide, nitrogen oxide and sulfur dioxide from flue gas using Chlorella sp. cultures, Academies Press, 2016.
Bioresour. Technol. 102 (2011) 9135–9142. [124] P.-H. Chiu, K. Soong, C.-N.N. Chen, Cultivation of two thermotolerant microal-
[93] B. Zhao, Y. Su, Process effect of microalgal-carbon dioxide fixation and biomass gae under tropical conditions: Influences of carbon sources and light duration on
production: A review, Renew. Sustain. Energy Rev. 31 (2014) 121–132. biomass and lutein productivity in four seasons, Bioresour. Technol. 212 (2016)
[94] D. Chaumont, Biotechnology of algal biomass production: a review of systems for 190–198.
outdoor mass culture, J. Appl. Phycol. 5 (1993) 593–604. [125] M. Acedo, J.R. Gonzalez Cena, K.M. Kiehlbaugh, K.L. Ogden, Coupling Carbon Cap-
[95] M. Xu, D. ou, Z. Xue, Y. Zhao, S. Sun, J. Liu, Enhancement of the photosynthetic ture from a Power Plant With Semi-automated Open Raceway Ponds For Microal-
and removal performance for microalgae-based technologies by co-culture strategy gae Cultivation, JoVE, 2020.
and strigolactone induction, Bioresour. Technol. 339 (2021) 125579. [126] I. de Godos, J.L. Mendoza, F.G. Acién, E. Molina, C.J. Banks, S. Heaven, F. Rogalla,
[96] S.J.P. Jegathese, M. Farid, Microalgae as a renewable source of energy: a niche Evaluation of carbon dioxide mass transfer in raceway reactors for microalgae cul-
opportunity, J. Renew. Energy 2014 (2014) 1–10. ture using flue gases, Bioresour. Technol. 153 (2014) 307–314.
[97] A. Jacob, A. Xia, J.D. Murphy, A perspective on gaseous biofuel production from [127] H. Hadiyanto, S. Elmore, T. Van Gerven, A. Stankiewicz, Hydrodynamic evaluations
micro-algae generated from CO2 from a coal-fired power plant, Appl. Energy 148 in high-rate algae pond (HRAP) design, Chem. Eng. J. 217 (2013) 231–239.
(2015) 396–402. [128] K. Sirikulrat, J. Pekkoh, C. Pumas, Illumination system for growth and net energy
[98] H. Znad, Microalgae culture technology for carbon dioxide biomitigation, in: Hand- ratio enhancement of Arthrospira (Spirulina) platensis outdoor cultivation in deep
book of Algal Science, Technology and Medicine, Elsevier, 2020, pp. 303–316. raceway pond, Bioresour. Technol. Rep. 14 (2021) 100661.
[99] A. Kumar, S. Ergas, X. Yuan, A. Sahu, Q. Zhang, J. Dewulf, F.X. Malcata, H. van [129] J. Cheng, Z. Yang, Q. Ye, J. Zhou, K. Cen, Enhanced flashing light effect with up-
Langenhove, Enhanced CO2 fixation and biofuel production via microalgae: recent -down chute baffles to improve microalgal growth in a raceway pond, Bioresour.
developments and future directions, Trend. Biotechnol. 28 (2010) 371–380. Technol. 190 (2015) 29–35.
[100] B. Wang, Y. Li, N. Wu, C.Q. Lan, CO2 bio-mitigation using microalgae, Appl. Mi- [130] S. Li, S. Luo, R. Guo, Efficiency of CO2 fixation by microalgae in a closed raceway
crobiol. Biotechnol. 79 (5) (2008) 707–718. pond, Bioresour. Technol. 136 (2013) 267–272.
[101] D.L. Sutherland, J. Park, P.J. Ralph, R. Craggs, Ammonia, pH and dissolved inor- [131] R.N. Singh, S. Sharma, Development of suitable photobioreactor for algae produc-
ganic carbon supply drive whole pond metabolism in full-scale wastewater high- tion – a review, Renew. Sustain. Energy Rev. 16 (2012) 2347–2353.
-rate algal ponds, Algal Res. 58 (2021) 102405. [132] A.P. Carvalho, L.A. Meireles, F.X. Malcata, Microalgal reactors: a review of enclosed
[102] A. Richmond, Open systems for the mass production of photoautotrophic microal- system designs and performances, Biotechnol. Progr. 22 (2006) 1490–1506.
gae outdoors: physiological principles, J. Appl. Phycol. 4 (1992) 281–286. [133] H.C. Greenwell, L.M.L. Laurens, R.J. Shields, R.W. Lovitt, K.J. Flynn, Placing mi-
[103] B. Zhao, Y. Su, Process effect of microalgal-carbon dioxide fixation and biomass croalgae on the biofuels priority list: a review of the technological challenges, J. R.
production: A review, Renew. Sustain. Energy Rev. 31 (2014) 121–132. Soc. Interface. 7 (2009) 703–726.
[104] J.N. Rogers, J.N. Rosenberg, B.J. Guzman, V.H. Oh, L.E. Mimbela, A. Ghassemi, [134] P.J. Schnurr, D.G. Allen, Factors affecting algae biofilm growth and lipid produc-
M.J. Betenbaugh, G.A. Oyler, M.D. Donohue, A critical analysis of paddlewheel– tion: A review, Renew. Sustain. Energy Rev. 52 (2015) 418–429.
driven raceway ponds for algal biofuel production at commercial scales, Algal Res. [135] S.S. Rosli, W.N. Amalina Kadir, C.Y. Wong, F.Y. Han, J.W. Lim, M.K. Lam, S. Yusup,
4 (2014) 76–88. W. Kiatkittipong, K. Kiatkittipong, A. Usman, Insight review of attached microal-
[105] Photobioreactors: production systems for phototrophic microorganisms, Appl. Mi- gae growth focusing on support material packed in photobioreactor for sustainable
crobiol. Biotechnol. 57 (2001) 287–293. biodiesel production and wastewater bioremediation, Renew. Sustain. Energy Rev.
[106] Y. Chisti, in: Large-Scale Production of Algal Biomass: Raceway Ponds, in: Algae 134 (2020) 110306.
Biotechnology, Springer International Publishing, 2016, pp. 21–40. [136] X. Xu, X. Gu, Zhongyang Wang, W. Shatner, Zhenjun Wang, Progress, challenges
[107] A. Parsy, L. Bidoire, M. Saadouni, M. Bahuaud, T. Elan, F. Périé, C. Sambusiti, and solutions of research on photosynthetic carbon sequestration efficiency of mi-
Impact of seasonal variations on Nannochloropsis oculata phototrophic productivity croalgae, Renew. Sustain. Energy Rev. 110 (2019) 65–82.
in an outdoor pilot scale raceway, Algal Res. 58 (2021) 102375. [137] M.J. Raeesossadati, H. Ahmadzadeh, M.P. McHenry, N.R. Moheimani, CO2 biore-
[108] N. Hossain, T.M.I. Mahlia, Progress in physicochemical parameters of microalgae mediation by microalgae in photobioreactors: Impacts of biomass and CO2 concen-
cultivation for biofuel production, Crit. Rev. Biotechnol. 39 (2019) 835–859. trations, light, and temperature, Algal Res. 6 (2014) 78–85.
[109] S. Sivakaminathan, J. Wolf, J. Yarnold, J. Roles, I.L. Ross, E. Stephens, G. Hender- [138] S. Huo, Z. Wang, S. Zhu, Q. Shu, L. Zhu, L. Qin, W. Zhou, P. Feng, F. Zhu, Z. Yuan,
son, B. Hankamer, Light guide systems enhance microalgae production efficiency R. Dong, Biomass accumulation of Chlorella Zofingiensis G1 cultures grown outdoors
in outdoor high-rate ponds, Algal Res. 47 (2020) 101846. in photobioreactors, Front. Energy Res. 6 (2018).
[110] J.L. Mendoza, M.R. Granados, I. de Godos, F.G. Acién, E. Molina, S. Heaven, [139] A. Alaswad, M. Dassisti, T. Prescott, A.G. Olabi, Technologies and developments
C.J. Banks, Oxygen transfer and evolution in microalgal culture in open raceways, of third generation biofuel production, Renew. Sustain. Energy Rev. 51 (2015)
Bioresour. Technol. 137 (2013) 188–195. 1446–1460.
[111] D. Chiaramonti, M. Prussi, D. Casini, M.R. Tredici, L. Rodolfi, N. Bassi, G.C. Zittelli, [140] J.-S. Chang, P.-L. Show, T.-C. Ling, C.-Y. Chen, S.-H. Ho, C.-H. Tan, D. Nagarajan,
P. Bondioli, Review of energy balance in raceway ponds for microalgae cultivation: W.-N. Phong, Photobioreactors, in: Current Developments in Biotechnology and
Re-thinking a traditional system is possible, Appl. Energy 102 (2013) 101–111. Bioengineering, Elsevier, 2017, pp. 313–352.
[112] S. Kumar, J. Cheng, W. Guo, K.A. Ali, Y. Song, Self-rotary propellers with clock- [141] R.N. Singh, S. Sharma, Development of suitable photobioreactor for algae produc-
wise/counterclockwise blades create spiral flow fields to improve mass transfer and tion – A review, Renew. Sustain. Energy Rev. 16 (2012) 2347–2353.
promote microalgae growth, Bioresour. Technol. 286 (2019) 121384. [142] V. Senatore, A. Buonerba, T. Zarra, G. Oliva, V. Belgiorno, J. Boguniewicz-Z-
[113] U. Suparmaniam, M.K. Lam, Y. Uemura, J.W. Lim, K.T. Lee, S.H. Shuit, Insights ablocka, V. Naddeo, Innovative membrane photobioreactor for sustainable CO2
capture and utilization, Chemosphere 273 (2021) 129682.

15
S. Paul, S. Bera, R. Dasgupta et al. Energy Nexus 4 (2021) 100032

[143] E. Aghaalipour, A. Akbulut, G. Güllü, Carbon dioxide capture with microalgae [164] V. De Laurentiis, D. Hunt, C. Rogers, Overcoming food security challenges within
species in continuous gas-supplied closed cultivation systems, Biochem. Eng. J. an Energy/Water/Food Nexus (EWFN) approach, Sustainability. 8 (2016) 95.
163 (2020) 107741. [165] I. Ghiat, F. Mahmood, R. Govindan, T. Al-Ansari, CO2 utilisation in agricultural
[144] M. Anjos, B.D. Fernandes, A.A. Vicente, J.A. Teixeira, G. Dragone, Optimization of greenhouses: A novel ‘plant to plant’ approach driven by bioenergy with carbon
CO2 bio-mitigation by Chlorella vulgaris, Bioresour. Technol. 139 (2013) 149–154. capture systems within the energy, water and food Nexus, Energy Convers. Manage.
[145] Y.K. Dasan, M.K. Lam, S. Yusup, J.W. Lim, P.L. Show, I.S. Tan, K.T. Lee, Cultiva- 228 (2021) 113668.
tion of Chlorella vulgaris using sequential-flow bubble column photobioreactor: A [166] J.F. Kim, E. Drioli, Transport membrane condenser heat exchangers to break the
stress-inducing strategy for lipid accumulation and carbon dioxide fixation, J. CO2 water-energy nexus—a critical review, Membranes. 11 (2020) 12.
Util. 41 (2020) 101226. [167] K. Lee, B.R. Bakshi, Energy-water-CO2 nexus of fossil fuel based power generation,
[146] S. Dey, A. Bhattacharya, P. Kumar, A. Malik, High-rate CO2 sequestration using a Adv. Carbon Manag. Technol. (2020) 184–202.
novel venturi integrated photobioreactor and subsequent valorization to microalgal [168] P.R.de C. Merschmann, E. Vasquez, A.S. Szklo, R. Schaeffer, Modeling water use de-
lipids, Green Chem. 22 (2020) 7962–7973. mands for thermoelectric power plants with CCS in selected Brazilian water basins,
[147] X. Jin, S. Gong, Z. Chen, J. Xia, W. Xiang, Potential microalgal strains for converting Int. J. Greenhouse Gas Control 13 (2013) 87–101.
flue gas CO2 into biomass, J. Appl. Phycol. 33 (2020) 47–55. [169] F. Guedes, A. Szklo, P. Rochedo, F. Lantz, L. Magalar, E.M.V. Arroyo, Climate-ener-
[148] A. Estrada-Graf, S. Hernández, M. Morales, Biomitigation of CO2 from flue gas by gy-water nexus in Brazilian oil refineries, Int. J. Greenhouse Gas Control 90 (2019)
Scenedesmus obtusiusculus AT-UAM using a hybrid photobioreactor coupled to a 102815.
biomass recovery stage by electro-coagulation-flotation, Environ Sci Pollut Res 27 [170] T. Al-Ansari, R. Govindan, A. Korre, Z. Nie, N. Shah, An energy, water and food
(2020) 28561–28574. nexus approach aiming to enhance food production systems through CO2 fertiliza-
[149] A. Aslam, S.R. Thomas-Hall, T.A. Mughal, P.M. Schenk, Selection and adaptation tion, Comput. Aid. Chem. Eng. 43 (2018) 1487–1492.
of microalgae to growth in 100% unfiltered coal-fired flue gas, Bioresour. Technol. [171] Solène Chiquier, Mathilde Fajardy, Niall Mac Dowell, The water-energy-carbon-
233 (2017) 271–283. land nexus: Optimising the BECCS supply chain, CO2 Summit III: Pathways to Car-
[150] A. Aslam, S.R. Thomas-Hall, T. Mughal, Q. Zaman, N. Ehsan, S. Javied, P.M. Schenk, bon Capture, Utilization, and Storage Deployment, Jen Wilcox (Colorado School
Heavy metal bioremediation of coal-fired flue gas using microalgae under different of Mines, USA) Holly Krutka (Tri-State Generation and Transmission Association-
CO2 concentrations, J. Environ. Manage. 241 (2019) 243–250. Simona Liguori (Colorado School of Mines, USA) Niall Mac Dowell (Imperial, US-
[151] H.-H. Chou, H.-Y. Su, X.-D. Song, T.-J. Chow, C.-Y. Chen, J.-S. Chang, T.-M. Lee, ACollege, United, 2017 https://dc.engconfintl.org/co2_summit3/4.
Isolation and characterization of Chlorella sp. mutants with enhanced thermo- and [172] M. Fajardy, S. Chiquier, N. Mac Dowell, Investigating the BECCS resource nexus: de-
CO2 tolerances for CO2 sequestration and utilization of flue gases, Biotechnol. Bio- livering sustainable negative emissions, Energy Environ. Sci. 11 (2018) 3408–3430.
fuels 12 (2019). [173] T. Al-Ansari, A. Korre, Z. Nie, N. Shah, Integration of greenhouse gas control tech-
[152] Y.C. a, C.X. a, How to narrow the CO2 gap from growth-optimal to flue gas levels by nologies within the energy, water and food nexus to enhance the environmental
using microalgae for carbon capture and sustainable biomass production, J. Clean. performance of food production systems, J. Clean. Prod. 162 (2017) 1592–1606.
Prod. 280 (2021) 124448. [174] J. Fouladi, A. AlNouss, T. Al-Ansari, Sustainable energy-water-food nexus integra-
[153] Y. Chen, L. Zhang, C. Xu, S. Vaidyanathan, Dissolved inorganic carbon speciation tion and optimization in eco-industrial parks, Comput. Chem. Eng. 146 (2021)
in aquatic environments and its application to monitor algal carbon uptake, Sci. 107229.
Total Environ. 541 (2016) 1282–1295. [175] T.S. Adebayo, A.O. Acheampong, Modelling the globalization-CO2 emission nexus
[154] L.I. Rodas-Zuluaga, L. Castañeda-Hernández, E.I. Castillo-Vacas, A. Gradiz-Menji- in Australia: evidence from quantile-on-quantile approach, Environ. Sci. Pollut.
var, I.Y. López-Pacheco, C. Castillo-Zacarías, L. Boully, H.M.N. Iqbal, R. Parra-Saldí- Res. (2021) 1–16.
var, Bio-capture and influence of CO2 on the growth rate and biomass composition [176] R. Govindan, T. Al-Ansari, A. Korre, N. Shah, Assessment of technology portfolios
of the microalgae Botryococcus braunii and Scenedesmus sp, J. CO2 Util. 43 (2021) with enhanced economic and environmental performance for the energy, water
101371. and food nexus, Comput. Aid. Chem. Eng. 43 (2018) 537–542.
[155] J. Fu, Y. Huang, Q. Liao, Xun Zhu, A. Xia, Xianqing Zhu, J.-S. Chang, Boosting [177] M. Sharifzadeh, R.K.T. Hien, N. Shah, China’s roadmap to low-carbon electricity
photo-biochemical conversion and carbon dioxide bio-fixation of Chlorella vulgaris and water: Disentangling greenhouse gas (GHG) emissions from electricity-water
in an optimized photobioreactor with airfoil-shaped deflectors, Bioresour. Technol. nexus via renewable wind and solar power generation, and carbon capture and
337 (2021) 125355. storage, Appl. Energy 235 (2019) 31–42.
[156] Y. Song, J. Cheng, X. Lai, W. Guo, W. Yang, Developing a three-dimensional tan- [178] I. Ghiat, T. Al-Ansari, A review of carbon capture and utilisation as a CO2 abate-
gential swirl plate photobioreactor to enhance mass transfer and flashlight effect ment opportunity within the EWF nexus, J. CO2 Util. 45 (2021) 101432.
for microalgal CO2 fixation, Chem. Eng. Sci. 244 (2021) 116837. [179] D. Kirikkaleli, New insights into an old issue: exploring the nexus between eco-
[157] K. Wu, K. Ying, J. Zhou, D. Liu, L. Liu, Y. Tao, J. Hanotu, X. Zhu, Z. Cai, Opti- nomic growth and CO2 emissions in China, Environ. Sci. Pollut. Res. 27 (2020)
mizing the growth of Haematococcus Pluvialis based on a novel microbubble-driven 40777–40786.
photobioreactor, SSRN J. (2021). [180] J. Wang, Z. Yu, X. Zeng, Y. Wang, K. Li, S. Deng, Water-energy-carbon nexus: A life
[158] N. Azhand, A. Sadeghizadeh, R. Rahimi, Effect of superficial gas velocity on CO2 cycle assessment of post-combustion carbon capture technology from power plant
capture from air by Chlorella vulgaris microalgae in an Airlift photobioreactor with level, J. Clean. Prod. 312 (2021) 127727.
external sparger, J. Environ. Chem. Eng. 8 (2020) 104022. [181] P. Brandl, S.M. Soltani, P.S. Fennell, N.M. Dowell, Evaluation of cooling require-
[159] P. Yaqoubnejad, H.A. Rad, M. Taghavijeloudar, Development a novel hexagonal ments of post-combustion CO2 capture applied to coal-fired power plants, Chem.
airlift flat plate photobioreactor for the improvement of microalgae growth that Eng. Res. Des. 122 (2017) 1–10.
simultaneously enhance CO2 bio-fixation and wastewater treatment, J. Environ. [182] M. Atilhan, R. Ullah, C.T. Yavuz, Carbon capture: Performance of porous covalent
Manage. 298 (2021) 113482. organic polymers for CO2 capture at elevated pressure, in: The Water-Food-Energy
[160] J. Xu, J. Cheng, X. Lai, X. Zhang, W. Yang, J.-Y. Park, H. Kim, L. Xu, Enhancing Nexus: Processes, Technologies, and Challenges, CRC Press, 2017, pp. 603–613.
microalgal biomass productivity with an optimized flow field generated by double [183] A. Al-Qahtani, A. González-Garay, A. Bernardi, Á. Galán-Martín, C. Pozo,
paddlewheels in a flat plate photoreactor with CO2 aeration based on numerical N.M. Dowell, B. Chachuat, G. Guillén-Gosálbez, Electricity grid decarbonisation
simulation, Bioresour. Technol. 314 (2020) 123762. or green methanol fuel? A life-cycle modelling and analysis of today′s transporta-
[161] A. AlNouss, G. McKay, T. Al-Ansari, A techno-economic-environmental study eval- tion-power nexus, Appl. Energy 265 (2020) 114718.
uating the potential of oxygen-steam biomass gasification for the generation of [184] M. Tajik Mansouri, M. Amidpour, J.M. Ponce-Ortega, Optimization of the inte-
value-added products, Energy Convers. Manage. 196 (2019) 664–676. grated power and desalination plant with algal cultivation system compromising
[162] P.-C. Chiang, S.-Y. Pan, in: Carbon Dioxide Mineralization and Utilization, Springer, the energy-water-environment nexus, Sustain. Energy Technol. Assess. 42 (2020)
Singapore, 2017, pp. 1–452. 100879.
[163] T. Al-Ansari, A. Korre, Z. Nie, N. Shah, Development of a life cycle assessment tool
for the assessment of food production systems within the energy, water and food
nexus, Sustain. Product. Consum. 2 (2015) 52–66.

16

You might also like