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<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">Front. Chem. Eng.</journal-id>
<journal-title>Frontiers in Chemical Engineering</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Front. Chem. Eng.</abbrev-journal-title>
<issn pub-type="epub">2673-2718</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="publisher-id">711971</article-id>
<article-id pub-id-type="doi">10.3389/fceng.2021.711971</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Chemical Engineering</subject>
<subj-group>
<subject>Review</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>Phase Separation in Anaerobic Digestion: A Potential for Easier Process Combination?</article-title>
<alt-title alt-title-type="left-running-head">Janesch et&#x20;al.</alt-title>
<alt-title alt-title-type="right-running-head">Phase Separation in Anaerobic Digestion</alt-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Janesch</surname>
<given-names>Eike</given-names>
</name>
<uri xlink:href="https://loop.frontiersin.org/people/1345769/overview"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Pereira</surname>
<given-names>Joana</given-names>
</name>
<uri xlink:href="https://loop.frontiersin.org/people/1452492/overview"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Neubauer</surname>
<given-names>Peter</given-names>
</name>
<uri xlink:href="https://loop.frontiersin.org/people/29927/overview"/>
</contrib>
<contrib contrib-type="author" corresp="yes">
<name>
<surname>Junne</surname>
<given-names>Stefan</given-names>
</name>
<xref ref-type="corresp" rid="c001">&#x2a;</xref>
<uri xlink:href="https://loop.frontiersin.org/people/31538/overview"/>
</contrib>
</contrib-group>
<aff>Bioprocess Engineering, Department of Biotechnology, Technische Universit&#xe4;t Berlin, <addr-line>Berlin</addr-line>, <country>Germany</country>
</aff>
<author-notes>
<fn fn-type="edited-by">
<p>
<bold>Edited by:</bold> <ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/804782/overview">Sergi Astals</ext-link>, University of Barcelona, Spain</p>
</fn>
<fn fn-type="edited-by">
<p>
<bold>Reviewed by:</bold> <ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/1318168/overview">Lucas Vassalle</ext-link>, Federal University of Minas Gerais, Brazil</p>
<p>
<ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/822138/overview">Cesar Huili&#xf1;ir Cur&#xed;o</ext-link>, University of Santiago, Chile</p>
</fn>
<corresp id="c001">&#x2a;Correspondence: Stefan Junne, <email>stefan.junne@tu-berlin.de</email>
</corresp>
<fn fn-type="other">
<p>This article was submitted to Environmental Chemical Engineering, a section of the journal Frontiers in Chemical Engineering</p>
</fn>
</author-notes>
<pub-date pub-type="epub">
<day>01</day>
<month>09</month>
<year>2021</year>
</pub-date>
<pub-date pub-type="collection">
<year>2021</year>
</pub-date>
<volume>3</volume>
<elocation-id>711971</elocation-id>
<history>
<date date-type="received">
<day>19</day>
<month>05</month>
<year>2021</year>
</date>
<date date-type="accepted">
<day>18</day>
<month>08</month>
<year>2021</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#xa9; 2021 Janesch, Pereira, Neubauer and Junne.</copyright-statement>
<copyright-year>2021</copyright-year>
<copyright-holder>Janesch, Pereira, Neubauer and Junne</copyright-holder>
<license xlink:href="http://creativecommons.org/licenses/by/4.0/">
<p>This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these&#x20;terms.</p>
</license>
</permissions>
<abstract>
<p>The flexibilization of bioenergy production has the potential to counteract partly other fluctuating renewable energy sources (such as wind and solar power). As a weather-independent energy source, anaerobic digestion (AD) can offer on-demand energy supply through biogas production. Separation of the stages in anaerobic digestion represents a promising strategy for the flexibilization of the fermentative part of biogas production. Segregation in two reactor systems facilitates monitoring and control of the provision of educts to the second methanogenic stage, thus controlling biogas production. Two-stage operation has proven to reach similar or even higher methane yields and biogas purities than single-stage operation in many different fields of application. It furthermore allows methanation of green hydrogen and an easier combination of material and energy use of many biogenic raw and residual biomass sources. A lot of research has been conducted in recent years regarding the process phase separation in multi-stage AD operation, which includes more than two stages. Reliable monitoring tools, coupled with effluent recirculation, bioaugmentation and simulation have the potential to overcome the current drawbacks of a sophisticated and unstable operation. This review aims to summarize recent developments, new perspectives for coupling processes for energy and material use and a system integration of AD for power-to-gas applications. Thereby, cell physiological and engineering aspects as well as the basic economic feasibility are discussed. As conclusion, monitoring and control concepts as well as suitable separation technologies and finally the data basis for techno-economic and ecologic assessments have to be improved.</p>
</abstract>
<kwd-group>
<kwd>two-stage digestion</kwd>
<kwd>feedstock flexibilization</kwd>
<kwd>methanation</kwd>
<kwd>on-demand production</kwd>
<kwd>bioprocess coupling</kwd>
</kwd-group>
<contract-sponsor id="cn001">Bundesministerium f&#xfc;r Wirtschaft und Energie<named-content content-type="fundref-id">10.13039/501100006360</named-content>
</contract-sponsor>
</article-meta>
</front>
<body>
<sec id="s1">
<title>Introduction</title>
<p>Flexible biogas production <italic>via</italic> anaerobic digestion (AD) can complement the energy production by fluctuating renewable wind and solar energy sources, which are typically affected by seasonality (<xref ref-type="bibr" rid="B103">Peters et&#x20;al., 2018</xref>). Additionally, the use of biogenic residues for biogas production, such as agricultural and forestry by-products and industrial as well as municipal residues encourages the implementation of circular bioeconomy concepts, while facilitating solid waste management. The competition for the utilization of natural resources, polluting emissions, and feedstock costs are reduced (<xref ref-type="bibr" rid="B4">Atasoy et&#x20;al., 2018</xref>; <xref ref-type="bibr" rid="B122">Theuerl et&#x20;al., 2019</xref>). In order to increase the potential of existing AD processes without multiplying the investment costs required for the installation of on-site gas storage, the fermentation itself can be operated dynamically. This can be achieved by using varying amounts of feedstock or alternating the feedstock sources. One promising approach to increase the flexibilization of the production rates is represented by process-phase separation. Hereby, the ideal conditions for every process phase can be controlled separately in each stage. Additionally, a coupling of energy and material use of various biogenic resources becomes feasible.</p>
<p>The advantages and disadvantages of phase separation in AD have been described in several research papers and reviews e.g. from <xref ref-type="bibr" rid="B24">Chatterjee and Mazumder (2019)</xref>, <xref ref-type="bibr" rid="B125">Van et&#x20;al. (2020)</xref> or <xref ref-type="bibr" rid="B85">Menzel et&#x20;al. (2020)</xref>. The present work aims to complement previous research on the topic, by highlighting the value-adding possibilities which can result from coupling the hydrolytic/acidogenic with the methanogenic stage of AD. The synergies obtained from phase separation and effluent recirculation in AD are discussed as means for the achievement of stable, affordable, and sustainable energy production. Furthermore, the potential for achieving value-added products beside biogas is highlighted. Challenges remain though, such as process disturbances caused by the overgrowth of phase-specific microorganisms brought in from feedstock, effects of inhibitors and the achievement of individual suitable feeding rates of substrates and co-factors at each process stage. Such hurdles can be minimized by improved process controllability and predictability, which can be achieved <italic>via</italic> improved process monitoring, which includes cell viability measures and, if known, the quick detection of potential inhibitors. Recent developments in this field are described in this review as they can support a robust operation in multi-stage AD. Additionally, a comprehensive summary of the recent approaches for flexible biogas production coupled with biological methanation or other bioprocesses is presented.</p>
</sec>
<sec id="s2">
<title>Phases of Anaerobic Digestion</title>
<p>AD is a complex process, in which various microorganisms are involved in degrading organic substrates under anaerobic conditions. In brief, AD is typically described with four metabolic phases as shown in <xref ref-type="fig" rid="F1">Figure&#x20;1</xref>. In the first step &#x2013; the hydrolysis - biomass which usually consists of insoluble organic polymers like proteins, lipids and carbohydrates is degraded by hydrolytic bacteria into soluble oligo- and monomers (<xref ref-type="bibr" rid="B57">Kaltschmitt et&#x20;al., 2016</xref>; <xref ref-type="bibr" rid="B107">Rabii et&#x20;al., 2019</xref>). Hydrolysis often acts as the bottleneck in AD processes as it demands a combination of enzymes and time to break the complex molecule structures of the substrate to overcome the steric hindrance. Mechanical, thermal, chemical, and biological pretreatment processes, as well as combinations thereof, have been reviewed and assessed for their potential to increase the efficiency of AD and shorten process times, e.g. in (<xref ref-type="bibr" rid="B3">Ariunbaatar et&#x20;al., 2014</xref>). In order to access the high-molecular, sterically blocked substances, microorganisms use exoenzymes like hydrolases. Most of these facultative anaerobic or strictly anaerobic hydrolytic microorganisms are very resilient against varying chemical and physical conditions. A recent review focused on the hydrolytic process stage in depth (<xref ref-type="bibr" rid="B85">Menzel et&#x20;al., 2020</xref>) among other previous reports.</p>
<fig id="F1" position="float">
<label>FIGURE 1</label>
<caption>
<p>Stages in an anaerobic digestion process (LCCA, long chain carboxylic acids; SCCA, short chain carboxylic acids).</p>
</caption>
<graphic xlink:href="fceng-03-711971-g001.tif"/>
</fig>
<p>In the second phase of AD, denoted as acidogenesis, fermentative bacteria degrade the resulting substances from the hydrolysis into low-molecular intermediates like amino acids, short-chain carboxylic acids (SCCAs), and alcohols. A description of the role of microbes within typical digestion consortia were summarized in <xref ref-type="bibr" rid="B107">Rabii et&#x20;al. (2019)</xref>.</p>
<p>In the next step, the acetogenesis, the intermediates from the acidogenesis are converted into acetic acid. Depending on the available substances, different ratios of acetic acid, carbon dioxide and hydrogen are formed by acetogenic bacteria like <italic>Acetobacterium</italic> or <italic>Clostridium</italic> species (<xref ref-type="bibr" rid="B16">Borja, 2011</xref>). The hydrolytic/acidogenic stage, eventually exhibiting acetogenic conversions, is also called dark fermentation (DF) or acid fermentation and typically operated with HRT of several days only (<xref ref-type="bibr" rid="B113">Rosgaard et&#x20;al., 2007</xref>; <xref ref-type="bibr" rid="B85">Menzel et&#x20;al., 2020</xref>; <xref ref-type="bibr" rid="B125">Van et&#x20;al., 2020</xref>). A pH-value of about 5.0 up to 6.0 is optimal, while a lower pH-value can lead to increased retention time; alkaline pH values may totally inhibit the process (<xref ref-type="bibr" rid="B138">Zhang et&#x20;al., 2005</xref>; <xref ref-type="bibr" rid="B89">Moestedt et&#x20;al., 2016</xref>).</p>
<p>In the final step of AD, strictly anaerobic methanogenic archaea transform hydrogen together with acetic acid and carbon dioxide into methane. In comparison to this conversion, that is restricted to a small group of microorganisms inside the archaea domain, the hydrogenotrophic methanogenesis is conducted by a wide variety of species as reviewed recently (<xref ref-type="bibr" rid="B57">Kaltschmitt et&#x20;al., 2016</xref>; <xref ref-type="bibr" rid="B20">Castellano-Hinojosa et&#x20;al., 2018</xref>; <xref ref-type="bibr" rid="B107">Rabii et&#x20;al., 2019</xref>). In this case, the reduction of carbon dioxide with hydrogen leads to the formation of methane. Growth of acetogens and methanogens is favored by mesophilic conditions and neutral pH-values. Since the anaerobic archaea show the slowest growth among most of the microbes in AD, they are the most fragile towards varying conditions and the presence of inhibitors like ammonia. Thus, in the widespread use of single-stage AD applications, the physical and chemical parameters of the system are adjusted in favor to keep these organisms vital (<xref ref-type="bibr" rid="B125">Van et&#x20;al., 2020</xref>). Typical representatives of archaea in biogas fermenters are described in more detail by <xref ref-type="bibr" rid="B132">Wirth et&#x20;al. (2012)</xref>.</p>
</sec>
<sec id="s3">
<title>Potentials of Phase Separation</title>
<p>Reactor types used in AD are typically continuously operated stirred tank reactors (STRs), upflow anaerobic sludge blankets (UASB) and plug-flow reactors (PFRs); the first two reactor designs are typically used for multi-stage AD. A lot of AD applications with UASBs can be found in tropical countries. These reactors benefit from their potential to handle high organic loading rates and their longevity and robustness due to the lack of moving parts like stirrers (<xref ref-type="bibr" rid="B9">Bischofsberger, 2005</xref>).</p>
<p>In the dominant single-stage stirred tank biogas reactors, all process phases are conducted in parallel. Beside the advantage of an intercellular hydrogen transfer, also some disadvantages of such a system exist: high loads of organic substrate or a sudden change in the feedstock composition can lead to acidification, when the hydrolytic and acidogenic or acetogenic reactions dominate and are conducted faster than the acid consumption by the acetoclastic organisms. This can lead to severe failures in fermentation and considerable down times (<xref ref-type="bibr" rid="B88">Moeller and Zehnsdorf, 2016</xref>). Although no detailed data about this has been published, the dominance of STRs over plug-flow reactors PFRs, in which a separation of phases is achieved due to the nature of the low axial mixing, is also caused by higher investment costs of the latter reactor technology. It is still not fully proven, however, if a PFR concept exhibits a higher robustness against flexible feedstock loads than a STR design due to the many possibilities of feedstock and operational conditions in the numerous published studies. Multi-stage AD applications, however, aim to combine some of the advantages of stirred tank and plug-flow concepts.</p>
<p>Theoretically, all four phases of AD can be divided and conducted in different reactors. Most of the hydrolytic and acidogenic bacteria, however, share similar optimal growth conditions. Generally, these are represented by mesophilic or thermophilic microbes, whose maximum growth is reached at slightly acidic pH-values of between 4.5 and 6.0. Aceto- and methanogens prefer neutral pH-values between 6.5 and 7.5. Thus, they differ in their nutritional demands, growth kinetics and temperature preferences compared to the hydrolytic and acidogenic microorganisms (<xref ref-type="bibr" rid="B125">Van et&#x20;al., 2020</xref>). In multi-stage AD processes, it becomes feasible to adjust the process parameters individually in each part of the reactor. Therefore, such a process design does not compromise as much between the different growth requirements of the microbes as in single-stage AD. In a typical multi-stage AD, the first stage comprises mostly of hydrolytic and acidogenic microorganisms while the subsequent stages contain mainly acetogenic and methanogenic microorganisms. By monitoring and controlling the pH-value, it is possible to separate these phases from each other with a low effort (<xref ref-type="bibr" rid="B24">Chatterjee and Mazumder, 2019</xref>; <xref ref-type="bibr" rid="B125">Van et&#x20;al., 2020</xref>).</p>
<p>Phase separation has proven to be beneficial to produce hydrogen-enriched biogas (10&#x2013;30% v/v) with a profitable process (<xref ref-type="bibr" rid="B30">Dahiya et&#x20;al., 2018</xref>). An AD process with phase separation can facilitate on-demand biogas production because the products of the hydrolysis can be added dynamically to the methanogenic stage. This way, the methane production can be enhanced for a certain time, e.g. by about 60% (<xref ref-type="bibr" rid="B76">Linke et&#x20;al., 2015</xref>). Leftover nutrients in the digestate can be used as biofertilizer, containing nitrogen in inorganic form (often over 60% (w/w) of total nitrogen), phosphorus, and potassium, characterized by a high bioavailability (<xref ref-type="bibr" rid="B28">Chojnacka et&#x20;al., 2020</xref>). A separate hydrolytic/acidogenic stage can save costs as other feedstock pre-treatment becomes useless (<xref ref-type="bibr" rid="B12">Blank and Hoffmann, 2011</xref>).</p>
<p>The phyla <italic>Proteobacteria, Bacteroidetes, Firmicutes and Chloroflexi</italic> can typically be found in AD broths (<xref ref-type="bibr" rid="B53">Jie et&#x20;al., 2014</xref>; <xref ref-type="bibr" rid="B77">Liu et&#x20;al., 2014</xref>; <xref ref-type="bibr" rid="B134">Wu et&#x20;al., 2016</xref>). These bacteria possess a higher natural resilience against disturbances and fluctuating process conditions than methanogens (<xref ref-type="bibr" rid="B57">Kaltschmitt et&#x20;al., 2016</xref>). When the first stage of an AD application is not dependent on the viability of methanogens due to separated phases, the whole process can gain more stability against a varying organic loading rate (OLR) and chemical inhibitors like oxygen, ammonia, and toxins, that are brought into the process by feedstock feeding. While different fermentation variants exist, like acetic-, butyric-, ethanol- or mixed-hydrolysis, <xref ref-type="bibr" rid="B85">Menzel et&#x20;al. (2020)</xref> consider acetic and butyric fermentation as most suitable for multi-stage AD applications. This type of fermentation is favored under thermophilic conditions at pH-values of between 5.0 and 6.0. Bacteria of the genus <italic>Clostridium</italic> release acetic and butyric acid and yields a biodegradability of up to 95% for the treatment of FW and rice straw in CSTR (<xref ref-type="bibr" rid="B121">Str&#xe4;uber et&#x20;al., 2012</xref>; <xref ref-type="bibr" rid="B26">Chen et&#x20;al., 2015</xref>). The metabolic activity of hydrolytic and acidogenic microorganisms is only inhibited at higher concentrations of SCCAs beyond 10&#xa0;g/L or more; much higher concentrations than it is usually the case for methanogens (<xref ref-type="bibr" rid="B139">Zhang et&#x20;al., 2017</xref>; <xref ref-type="bibr" rid="B24">Chatterjee and Mazumder, 2019</xref>).</p>
<p>AD is typically operated under either mesophilic (35&#x2013;39&#xb0;C) or thermophilic conditions (50&#x2013;60&#xb0;C). While thermophilic AD provides shorter HRT, digestion under mesophilic conditions is commonly considered as a slower, but rather stable process (<xref ref-type="bibr" rid="B125">Van et&#x20;al., 2020</xref>) with lower energy costs (<xref ref-type="bibr" rid="B38">Fern&#xe1;ndez-Rodr&#xed;guez et&#x20;al., 2016</xref>). A combination of hydrolysis and acidogenesis in a separate stage offers the possibility of temperature-gradients between the stages. This is of particular importance for the treatment of residues with high solid-contents like organic fractions of municipal solid waste (OFMSW) (<xref ref-type="bibr" rid="B38">Fern&#xe1;ndez-Rodr&#xed;guez et&#x20;al., 2016</xref>). Thermophilic operation, on the other side, promotes the deactivation of infectious pathogens as present in biogenic residues (<xref ref-type="bibr" rid="B142">Zhao and Liu, 2019</xref>). According to <xref ref-type="bibr" rid="B100">Pandey and Soupir (2011)</xref>, the inactivation rate of <italic>Escherichia</italic> coli, as a representative for pathogenic organisms is 15-fold higher at 52&#xb0;C than at 37&#xb0;C. <xref ref-type="bibr" rid="B38">Fern&#xe1;ndez-Rodr&#xed;guez et&#x20;al. (2016)</xref> showed an application with up to 34% higher removal rates of VS and increased methane production in a two-phase AD operated with temperature combinations. By this a compromise between a purely mesophilic or thermophilic operation is&#x20;made.</p>
<p>In order to achieve new opportunities for a flexible feedstock load and for demand-driven biogas production, research has been performed on multi-stage AD, especially in two-stage concepts. Several strategies and scenarios have been described, in which existing plant infrastructure is re-engineered to increase the production flexibility within multi-stage concepts. Other publications have reviewed some of these aspects regarding the OFMSW (<xref ref-type="bibr" rid="B24">Chatterjee and Mazumder, 2019</xref>) and food waste (FW) (<xref ref-type="bibr" rid="B120">Srisowmeya et&#x20;al., 2020</xref>), as well as for process configurations (<xref ref-type="bibr" rid="B125">Van et&#x20;al., 2020</xref>) and mixed gas production(<xref ref-type="bibr" rid="B47">Hans and Kumar, 2019</xref>). Rajendran and co-authors focused on techno-economic assessments and related investments and operational costs under the consideration of mono-digester plants (<xref ref-type="bibr" rid="B109">Rajendran et&#x20;al., 2020</xref>).</p>
<p>Typical characteristics of multi-stage AD are summarized in <xref ref-type="table" rid="T1">Table&#x20;1</xref>. The following chapters will further describe recent advances in more detail, including potential strategies to increase process robustness with monitoring and control tools, and the systemic integration into energy and biomaterial production&#x20;grids.</p>
<table-wrap id="T1" position="float">
<label>TABLE 1</label>
<caption>
<p>Characteristics of stage separation in anaerobic digestion.</p>
</caption>
<table>
<thead valign="top">
<tr>
<th align="left">Application</th>
<th align="center">Advantages</th>
<th align="center">Disadvantages</th>
<th align="center">Typical process arrangement</th>
</tr>
</thead>
<tbody valign="top">
<tr>
<td rowspan="4" align="left">Single-stage</td>
<td align="left">&#x2022; Low costs</td>
<td align="left">&#x2022; Risk of quick acidification</td>
<td rowspan="4" align="left">Hydrolysis/acidogenesis/acetogenesis/methanogenesis</td>
</tr>
<tr>
<td align="left">&#x2022; Applicable for very high/low TS-contents</td>
<td align="left">&#x2022; Repression of methanogens by inhibitors from the substrate (e.g. NH<sub>3</sub>)</td>
</tr>
<tr>
<td align="left">&#x2022; Established process</td>
<td align="left">&#x2022; Risk of bacterial overgrowth</td>
</tr>
<tr>
<td align="left"/>
<td align="left">&#x2022; No recovery of side products</td>
</tr>
<tr>
<td rowspan="3" align="left">Two-stage</td>
<td align="left">&#x2022; Recovery of side products</td>
<td align="left">&#x2022; High costs</td>
<td align="left">1. Stage: hydrolysis/acidogenesis</td>
</tr>
<tr>
<td align="left">&#x2022; Temperature-phased</td>
<td align="left">&#x2022; Not efficient for high TS-contents</td>
<td align="left">2. Stage: acetogenesis/methanogenesis</td>
</tr>
<tr>
<td align="left"/>
<td align="left">&#x2022; Disturbed intercellular hydrogen exchange</td>
<td align="left"/>
</tr>
<tr>
<td rowspan="3" align="left">Three-stage</td>
<td align="left">&#x2022; Recovery of side products</td>
<td align="left">&#x2022; Very high costs and operational effort</td>
<td align="left">1. Stage: hydrolysis/acidogenesis</td>
</tr>
<tr>
<td align="left">&#x2022; High hydrolysis efficiency</td>
<td align="left">&#x2022; Lack of research on pilot scale</td>
<td align="left">2. Stage: acidogenesis</td>
</tr>
<tr>
<td align="left">&#x2022; Shock load resistant</td>
<td align="left">&#x2022; Disturbed intercellular hydrogen exchange</td>
<td align="left">3. Stage: acetogenesis/methanogenesis</td>
</tr>
</tbody>
</table>
</table-wrap>
</sec>
<sec id="s4">
<title>Two-Stage Anaerobic Digestion</title>
<p>Two-stage AD is the most widely studied design within multi-phase processes. Recent work focused on operational optimization and the application of feedstock that is difficult to be degraded. <xref ref-type="bibr" rid="B71">Li et&#x20;al. (2017)</xref> published results for an OFMSW treatment with a two-phase AD application. A setup of three 20&#xa0;L STRs was used, the first two for the combination of hydrolysis and acidogenesis, similar to the first stage of a two-stage anaerobic digester. While the single-stage operation achieved a biogas production of 540&#xa0;ml/g-VS, the two-stage process reached 710&#xa0;ml/g-VS at a 30% higher OLR. The results of this study show that two-stage AD is not necessarily better than a single-stage AD in terms of substrate-specific biogas production yields, but might offer the possibility of higher loading and production rates. The net energetic production of a two-stage anaerobic digester for a substrate mixture consisting of whey and glycerine was compared to a single-stage system by <xref ref-type="bibr" rid="B79">Lovato et&#x20;al. (2020)</xref>. The authors concluded that the energy production from the two-stage AD (7.0&#x20;MJ/kg-COD<sub>removed</sub>) makes it profitable. <xref ref-type="bibr" rid="B43">Ghanimeh et&#x20;al. (2019)</xref> investigated the biogas production performance of a single- (STR, 9&#xa0;L) and a two-stage thermophilic anaerobic digester. The two-stage digester showed better overall degradation rates and better biogas quality: at an average OLR between 2.0 and 2.4&#xa0;g-VS/(L&#x2219;d), the reduction of total COD was nearly 80% higher in the multi-stage process compared to the mono-digester. The methane content of the biogas reached 45 and 54% in the single- and two-stage process design, respectively (<xref ref-type="bibr" rid="B43">Ghanimeh et&#x20;al., 2019</xref>).</p>
<p>Two-stage AD has the potential to produce desulfurized biogas without a subsequent (external) desulfurization. The first stage of the AD application is controlled to favor the coexistence of acidogenic and sulfate reducing bacteria. A sulfate reduction in the first stage consequently reduces the hydrogen sulfide (H<sub>2</sub>S) production in the methanogenic stage (<xref ref-type="bibr" rid="B123">Tijani et&#x20;al., 2018</xref>). <xref ref-type="bibr" rid="B137">Yun et&#x20;al. (2017)</xref> were able to reduce the H<sub>2</sub>S-content in the biogas in a two-stage AD system (STR, UASB) by nearly 90%, compared to a conventional single-stage digester. The first stage of their application acted as a sulfidogenic-acidogenic-reactor with a sulfate reduction of 70% at an optimum pH-value of 5.5. As a model substrate, the authors used glucose combined with sodium sulfate (<xref ref-type="bibr" rid="B137">Yun et&#x20;al., 2017</xref>). Similar results were described by <xref ref-type="bibr" rid="B123">Tijani et&#x20;al. (2018)</xref>, who examined the desulfurization of biogas in a two-stage system consisting of a shear-loop anaerobic bed and an anaerobic PFR&#x20;for the treatment of palm oil mill waste. They considered a pH-value of 5.4 as optimal for the sulfidogenic-acidogenic stage. The first stage of their application was able to reduce the sulfate by 75%, and the biogas from the methanogenic stage was suitable for electricity production without H<sub>2</sub>S removal (<xref ref-type="bibr" rid="B123">Tijani et&#x20;al., 2018</xref>). <xref ref-type="bibr" rid="B39">Flores-Cort&#xe9;s et&#x20;al. (2021)</xref> used a two-stage anaerobic nitrate-reducing bioreactor to desulfurize H<sub>2</sub>S-rich biogas; 95% of H<sub>2</sub>S was oxidized.</p>
<p>As described before, depending on the substrate, two-stage operation can, beside other benefits, reach higher energy production, methane yields and methane ratios in the biogas within shorter HRT than single-staged processes in different pilot-scale studies, e.g. for the thermophilic treatment of the OFMSW (<xref ref-type="bibr" rid="B43">Ghanimeh et&#x20;al., 2019</xref>) or the digestion of food waste (FW) (<xref ref-type="bibr" rid="B45">Gioannis et&#x20;al., 2017</xref>). There is, however, still room for improvement. One major challenge is the interspecies-hydrogen transfer. The hydrogen produced by the acidogens is released in a different tank than the one with the hydrogen-consuming methanogens, that make use of it. As hydrogen has a very low solubility in water, it has to be ensured that enough hydrogen is dissolved in the second stage of two-stage AD or hydrogen has to be released in the off-gas, thus lowering the carbon dioxide binding capacity of the biological methanation. High-pressure two-stage AD represents an approach to enrich biogas with methane, without the need for external purification. <xref ref-type="bibr" rid="B86">Merkle et&#x20;al. (2017)</xref> investigated the influence of high pressure up to 50&#x20;bar on a two-stage AD application, consisting of a leach bed reactor and an anaerobic filter, fed with maize and grass silage. The methanogenic reactor was operated at 37&#xb0;C, an OLR of between 4.2 and 4.4&#xa0;g-COD/(L&#x2219;d), pH-values of about 6.6 and pressures of 10, 25 and 50 bar. While the specific methane yield decreased from 0.33 to 0.04&#xa0;L/(g-COD) with an increased pressure from 10 to 50 bar, the methane content in the biogas increased by 11% (to finally 90%) under these conditions. As a result, the biogas could be transferred directly into the gas grid without additional purification or pressurization (<xref ref-type="bibr" rid="B86">Merkle et&#x20;al., 2017</xref>). <xref ref-type="bibr" rid="B69">Lemmer et&#x20;al. (2015)</xref> have also reported an increase in the methane content from 70 to 77% when increasing the pressure from 1 to 9&#x20;bar in a two-stage AD composed by a leach bed reactor for a separate acidogenesis at 55&#xb0;C, and a methanogenic stage at 37&#xb0;C at an OLR of 5&#xa0;g-COD/(L&#x2219;d) of maize and grass silage. The application of high pressure in two-stage AD systems leads, however, to a decreasing pH-value, which consequently effects the methane production negatively (<xref ref-type="bibr" rid="B69">Lemmer et&#x20;al., 2015</xref>). Thus, <xref ref-type="bibr" rid="B69">Lemmer et&#x20;al. (2015)</xref> tested, if a higher ammonium content in the methanogenic stage can counteract this issue by rising the buffer capacity. While the methane content of the biogas rose, the specific biogas yield decreased.</p>
<p>Furthermore and most important, concepts for an easy and cheap achievement of a two-stage process at existing biogas plants have to be accomplished, since the yearly numbers of new plants is slowing down (<xref ref-type="bibr" rid="B36">European Biogas Association, 2019</xref>). The &#x201c;ReBi 2.0&#x201d; (variable biogas production) from the Fraunhofer IEE represents a concept for upgrading existing biogas plants into variable biogas producers, which relies on the use of effluents enriched with SCCAs in the methanogenesis. After a hydrolytic stage, a phase separator enables the storage of the SCCAs-rich liquid in a storage tank. The solid effluents are digested in a conventional fermenter for continuous biogas production. The easily degradable SCCAs in turn are transferred to a fixed bed reactor, depending on the current demand of biogas. Experiments in a large-scale facility provided promising results with amounts of up to 70% (v/v) of methane in the biogas (<xref ref-type="bibr" rid="B41">Fraunhofer IEE, 2018</xref>).</p>
</sec>
<sec id="s5">
<title>Three-Stage Processes</title>
<p>Research on three-stage applications has proven, that the process conditions of AD can be further optimized. There exist different concepts for the separation of the process phases between the three stages. The first one is to separate the acetogens from the methanogens as they possess different nutritional requirements, resulting in an order of <italic>1</italic>) hydrolysis/acidogenesis, <italic>2</italic>) acetogenesis and <italic>3</italic>) methanogenesis (<xref ref-type="bibr" rid="B61">Kim et&#x20;al., 2006</xref>; <xref ref-type="bibr" rid="B62">Kim et&#x20;al., 2008</xref>). As the interspecies hydrogen transfer is a critical factor in multi-stage AD, the second concept is to rather split up hydrolysis and acidogenesis than to separate the acetogens and methanogens. This leads to the process sequence <italic>1</italic>) hydrolysis, <italic>2</italic>) acidogenesis, and <italic>3</italic>) acetogenesis/methanogenesis, as described for several cases (<xref ref-type="bibr" rid="B139">Zhang et&#x20;al., 2017</xref>; <xref ref-type="bibr" rid="B24">Chatterjee and Mazumder, 2019</xref>; <xref ref-type="bibr" rid="B125">Van et&#x20;al., 2020</xref>). A review of <xref ref-type="bibr" rid="B24">Chatterjee and Mazumder (2019)</xref> in contrast, refers to the stage separation order <italic>1</italic>) hydrolysis, <italic>2</italic>) acidogenesis/acetogenesis and <italic>3</italic>) methanogenesis, mainly due to the adverse effect of mixing, which is required for the homogenization of waste in the first&#x20;stage.</p>
<p>One of the first studies on three-stage AD originate from <xref ref-type="bibr" rid="B60">Kim et&#x20;al. (2000)</xref>. Under mesophilic conditions, FW was treated in a STR for hydrolysis/acidogenesis and two UASB for acidogenesis/acetogenesis/methanogenesis. Production rates of up to 700&#xa0;ml biogas/(g VS) with a methane content of 72% were achieved. The enhanced degradation of three-stage AD was confirmed by COD reduction rates of over 90%. Back in 2005, Salsali et&#x20;al. showed that three-stage AD for the treatment of waste activated sludge can provide higher methane yields than two-stage digesters (<xref ref-type="bibr" rid="B114">Salsali et&#x20;al., 2005</xref>). A maximum of over 650&#xa0;ml biogas/(g VS) were reached in their mesophilic application, operated with three STRs. A three-stage AD application with a focus on an enhanced hydrolysis in the first stage was compared to a single- and two-stage process design by <xref ref-type="bibr" rid="B139">Zhang et&#x20;al. (2017)</xref>. Their FW-fed digester consisted of three chambers, responsible for hydrolysis, acidogenesis and methanogenesis in a sequential arrangement. The enhanced hydrolysis decreased the reduction of VS by half compared to the two-stage digester (44 vs 83% w/w). In addition, the methane yield of the three-stage application increased by up to 54%; the methane content of the biogas rose to nearly 70% (v/v), assumingly due to an intensified hydrolysis compared to the two-stage process (<xref ref-type="bibr" rid="B139">Zhang et&#x20;al., 2017</xref>). Similar results were described by <xref ref-type="bibr" rid="B141">Zhang et&#x20;al. (2020)</xref>. The authors used a three-stage thermophilic reactor to treat a mixture of FW and horticultural waste. Methane yields were (with about 0.42&#xa0;L/g VS) 31&#x2013;45% higher than those in one- and two-stage reactors. The reduction of VS (63%) increased by over 60% compared to the single-stage system (<xref ref-type="bibr" rid="B141">Zhang et&#x20;al., 2020</xref>). The anaerobic treatment of tofu whey wastewater (COD: 15.9&#xa0;g/L) in a three-stage reactor was described by <xref ref-type="bibr" rid="B130">Rani et&#x20;al. (2020)</xref>. The authors used a system which consisted of three 10&#xa0;L packed bed reactors. Due to the phase separation, which was indicated by the respective pH-values, the system was able to resist hydraulic shock loads (<xref ref-type="bibr" rid="B130">Rani et&#x20;al., 2020</xref>). It was possible to maintain the biogas production rate (20&#xa0;L/d) as well as the pH value (around 5.0 in the first two reactors and around 7.0 in the third reactor) and the COD at the outflow after the organic load was increased 12-fold for 1&#xa0;h (0.33 vs 4.0&#xa0;L/h). The ratio of alkalinity to volatile SCCAs, which rose during the shock load, was reduced and stabilized within 8&#xa0;h after the shock load. Superior process performance has also been reported for a three-stage anaerobic system using sequencing batch reactors, when compared to both single- and two-stage anaerobic processes treating several types of wastewaters (<xref ref-type="bibr" rid="B55">Jiraprasertwong et&#x20;al., 2018</xref>). With an optimum COD loading rate of 18&#xa0;kg/(m<sup>3</sup>&#x2219;d), the process achieved 686&#xa0;ml CH<sub>4</sub>/g-COD, with an energy yield of 22.5&#xa0;kJ/g-COD, and an overall COD removal of 92%. The system performance has been related to the high microbial concentrations reached in the bioreactors, high alkalinity, and adequate pH, with values of 5.5, 6.0&#x2013;7.0, and 7.5 in the first, second, and third stages, respectively. Several typical residual resources contain lignocellulose. For the treatment of such feedstock, a separate hydrolytic stage, which relied on white rot fungi, was able to degrade lignin enzymatically (<xref ref-type="bibr" rid="B127">Wan and Li, 2012</xref>; <xref ref-type="bibr" rid="B84">Meegoda et&#x20;al., 2018</xref>).</p>
<p>Further examples for AD applications with one, two and three stages and their respective process conditions are summarized in <xref ref-type="table" rid="T2">Table&#x20;2</xref>.</p>
<table-wrap id="T2" position="float">
<label>TABLE 2</label>
<caption>
<p>Examples for one-, two- and three-stage phase separation applications in anaerobic digestion.</p>
</caption>
<table>
<thead valign="top">
<tr>
<th align="left">Feedstock</th>
<th align="center">Reactor type 1st, 2nd, 3rd</th>
<th align="center">TS [%]</th>
<th align="center">OLR [g-VS/(L&#x2219;d)]</th>
<th align="center">HRT [d]</th>
<th align="center">pH</th>
<th align="center">Biogas yield [ml-CH<sub>4</sub>/(g-VS)]</th>
<th align="center">Temp</th>
<th align="center">Reference</th>
</tr>
</thead>
<tbody valign="top">
<tr>
<td align="left">WAS</td>
<td align="left">STR</td>
<td align="center">4.2</td>
<td align="center">-</td>
<td align="center">15</td>
<td align="center">7</td>
<td align="center">240</td>
<td align="left">mesophilic</td>
<td align="left">
<xref ref-type="bibr" rid="B49">Heng et&#x20;al. (2021)</xref>
</td>
</tr>
<tr>
<td align="left">Ensiled OFMSW</td>
<td align="left">Batch reactor</td>
<td align="center">12&#x2013;28</td>
<td align="center">-</td>
<td align="center">25</td>
<td align="center">6.0&#x2013;8.2</td>
<td align="center">431</td>
<td align="left">mesophilic</td>
<td align="left">
<xref ref-type="bibr" rid="B21">Castell&#xf3;n-Zelaya and Gonz&#xe1;lez-Mart&#xed;nez (2021)</xref>
</td>
</tr>
<tr>
<td align="left">MSW and fly ash</td>
<td align="left">STR</td>
<td align="center">9.72</td>
<td align="center">-</td>
<td align="center">45</td>
<td align="center">7.2&#x2013;7.5</td>
<td align="center">268&#x2013;287</td>
<td align="left">mesophilic</td>
<td align="left">
<xref ref-type="bibr" rid="B82">Markphan et&#x20;al. (2020)</xref>
</td>
</tr>
<tr>
<td align="left">OFMSW</td>
<td align="left">STR</td>
<td align="center">1.75</td>
<td align="center">1.35</td>
<td align="center">25</td>
<td align="center">7.94</td>
<td align="center">404</td>
<td align="left">thermophilic</td>
<td align="left">
<xref ref-type="bibr" rid="B116">Schievano et&#x20;al. (2012)</xref>
</td>
</tr>
<tr>
<td align="left">Sewage sludge</td>
<td align="left">STR</td>
<td align="center">4.0&#x2013;5.2</td>
<td align="center">2.1&#x2013;2.5</td>
<td align="center">15</td>
<td align="center">-</td>
<td align="center">260&#x2013;306</td>
<td align="left">mesophilic</td>
<td align="left">
<xref ref-type="bibr" rid="B114">Salsali et&#x20;al. (2005)</xref>
</td>
</tr>
<tr>
<td align="left">Fruit waste</td>
<td align="left">micro digester</td>
<td align="center">0.25</td>
<td align="center">-</td>
<td align="center">30</td>
<td align="center">7.5&#x2013;8.5</td>
<td align="center">610<xref ref-type="table-fn" rid="Tfn1">
<sup>a</sup>
</xref>
</td>
<td align="left">mesophilic</td>
<td align="left">
<xref ref-type="bibr" rid="B23">Chanakya and Shwetmala (2017)</xref>
</td>
</tr>
<tr>
<td rowspan="2" align="left">Sugar molasses</td>
<td align="left">Packed bed</td>
<td rowspan="2" align="center">-</td>
<td align="center">34</td>
<td align="center">0.55&#x2013;0.74</td>
<td align="center">4.5&#x2013;5.2</td>
<td rowspan="2" align="center">324<xref ref-type="table-fn" rid="Tfn2">
<sup>b</sup>
</xref>
</td>
<td align="left">mesophilic</td>
<td rowspan="2" align="left">
<xref ref-type="bibr" rid="B32">Detman et&#x20;al. (2017)</xref>
</td>
</tr>
<tr>
<td align="left">UASB</td>
<td align="center">-</td>
<td align="center">6.71</td>
<td align="center">6.5&#x2013;7.6</td>
<td align="left">mesophilic</td>
</tr>
<tr>
<td rowspan="2" align="left">Oily FW</td>
<td align="left">STR</td>
<td align="center">3.57</td>
<td align="center">14.2</td>
<td align="center">3</td>
<td align="center">5.36</td>
<td rowspan="2" align="center">450</td>
<td rowspan="2" align="left">thermophilic mesophilic</td>
<td rowspan="2" align="left">
<xref ref-type="bibr" rid="B133">Wu et&#x20;al. (2015)</xref>
</td>
</tr>
<tr>
<td align="left">STR</td>
<td align="center">2</td>
<td align="center">2.6</td>
<td align="center">12</td>
<td align="center">7.59</td>
</tr>
<tr>
<td rowspan="2" align="left">MSW</td>
<td align="left">STR</td>
<td align="center">3.9</td>
<td align="center">13</td>
<td align="center">7.5</td>
<td align="center">5.5&#x2013;6</td>
<td rowspan="2" align="center">540</td>
<td align="left">mesophilic</td>
<td rowspan="2" align="left">
<xref ref-type="bibr" rid="B71">Li et&#x20;al. (2017)</xref>
</td>
</tr>
<tr>
<td align="left">STR</td>
<td align="center">-</td>
<td align="center">3.8</td>
<td align="center">15</td>
<td align="center">-</td>
<td align="left">mesophilic</td>
</tr>
<tr>
<td rowspan="2" align="left">Chicken manure</td>
<td align="left">glas vessel</td>
<td rowspan="2" align="center">3.7</td>
<td rowspan="2" align="center">2.2</td>
<td align="center">2</td>
<td align="center">6.3&#x2013;6.8</td>
<td rowspan="2" align="center">554</td>
<td align="left">mesophilic</td>
<td rowspan="2" align="left">
<xref ref-type="bibr" rid="B31">Dalk&#x131;l&#x131;c and Ugurlu (2015)</xref>
</td>
</tr>
<tr>
<td align="left">glas vessel</td>
<td align="center">10</td>
<td align="center">7.7&#x2013;8</td>
<td align="left">thermophilic</td>
</tr>
<tr>
<td rowspan="2" align="left">FW, grass, chicken manure</td>
<td align="left">batch reactor</td>
<td rowspan="2" align="center">20</td>
<td rowspan="2" align="center">4</td>
<td rowspan="2" align="center">30</td>
<td align="center">4.5&#x2013;7.5</td>
<td rowspan="2" align="center">113</td>
<td align="left">mesophilic</td>
<td rowspan="2" align="left">
<xref ref-type="bibr" rid="B74">Li W. et&#x20;al. (2018)</xref>
</td>
</tr>
<tr>
<td align="left">batch reactor</td>
<td align="center">6.6&#x2013;7.5</td>
<td align="left">mesophilic</td>
</tr>
<tr>
<td rowspan="2" align="left">slaughterhouse blood waste</td>
<td align="left">tank reactor</td>
<td rowspan="2" align="center">2.8</td>
<td align="center">1.2</td>
<td align="center">11.1</td>
<td align="center">6&#x2013;6.2</td>
<td rowspan="2" align="center">384<xref ref-type="table-fn" rid="Tfn2">
<sup>b</sup>
</xref>
</td>
<td align="left">mesophilic</td>
<td rowspan="2" align="left">
<xref ref-type="bibr" rid="B128">Wang et&#x20;al. (2018)</xref>
</td>
</tr>
<tr>
<td align="left">tank reactor</td>
<td align="center">0.4&#x2013;1</td>
<td align="center">24.2</td>
<td align="center">7&#x2013;7.5</td>
<td align="left">mesophilic</td>
</tr>
<tr>
<td rowspan="3" align="left">Ethanol wastewater</td>
<td align="left">SBR</td>
<td align="center">3.17</td>
<td align="center">15&#x2013;21<xref ref-type="table-fn" rid="Tfn3">
<sup>c</sup>
</xref>
</td>
<td rowspan="3" align="center">-</td>
<td align="center">5.5</td>
<td rowspan="3" align="center">686<xref ref-type="table-fn" rid="Tfn2">
<sup>b</sup>
</xref>
</td>
<td align="left">mesophilic</td>
<td rowspan="3" align="left">
<xref ref-type="bibr" rid="B55">Jiraprasertwong et&#x20;al. (2018)</xref>
</td>
</tr>
<tr>
<td align="left">SBR</td>
<td align="center">-</td>
<td align="center">-</td>
<td align="center">6&#x2013;7</td>
<td align="left">mesophilic</td>
</tr>
<tr>
<td align="left">SBR</td>
<td align="center">-</td>
<td align="center">-</td>
<td align="center">7.2&#x2013;7.5</td>
<td align="left">mesophilic</td>
</tr>
<tr>
<td rowspan="3" align="left">Cassava wastewater</td>
<td align="left">UASB</td>
<td rowspan="3" align="center">-</td>
<td align="center">5&#x2013;18<xref ref-type="table-fn" rid="Tfn3">
<sup>c</sup>
</xref>
</td>
<td rowspan="3" align="center">-</td>
<td align="center">5.5</td>
<td rowspan="3" align="center">328<xref ref-type="table-fn" rid="Tfn2">
<sup>b</sup>
</xref>
</td>
<td align="left">mesophilic</td>
<td rowspan="3" align="left">
<xref ref-type="bibr" rid="B56">Jiraprasertwong et&#x20;al. (2019)</xref>
</td>
</tr>
<tr>
<td align="left">UASB</td>
<td align="center">-</td>
<td align="center">6.8</td>
<td align="left">mesophilic</td>
</tr>
<tr>
<td align="left">UASB</td>
<td align="center">-</td>
<td align="center">-</td>
<td align="left">mesophilic</td>
</tr>
<tr>
<td rowspan="3" align="left">FW</td>
<td align="left">STR</td>
<td align="center">17.5</td>
<td align="center">22&#x2013;22.8</td>
<td align="center">2</td>
<td align="center">5&#x2013;5.5</td>
<td rowspan="3" align="center">650&#x2013;700</td>
<td rowspan="3" align="left">mesophilic (each stage)</td>
<td rowspan="3" align="left">
<xref ref-type="bibr" rid="B60">Kim et&#x20;al. (2000)</xref>
</td>
</tr>
<tr>
<td align="left">UASB</td>
<td align="center">3</td>
<td align="center">25&#x2013;27.4</td>
<td align="center">2</td>
<td align="center">5&#x2013;5.5</td>
</tr>
<tr>
<td align="left">UASB</td>
<td align="center">16</td>
<td align="center">12&#x2013;18.8</td>
<td align="center">12</td>
<td align="center">7.6&#x2013;7.9</td>
</tr>
<tr>
<td rowspan="3" align="left">WAS</td>
<td align="left">STR</td>
<td align="center">4.6</td>
<td rowspan="3" align="center">2.13&#x2013;2.53 (each stage)</td>
<td rowspan="3" align="center">5 (each stage)</td>
<td rowspan="3" align="center">8 (each stage)</td>
<td rowspan="3" align="center">559&#x2013;664</td>
<td rowspan="3" align="left">mesophilic (each stage)</td>
<td rowspan="3" align="left">
<xref ref-type="bibr" rid="B114">Salsali et&#x20;al. (2005)</xref>
</td>
</tr>
<tr>
<td align="left">STR</td>
<td align="center">3.5</td>
</tr>
<tr>
<td align="left">STR</td>
<td align="center">-</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn>
<p>WAS, waste activated sludge; OFMSW, organic fraction of municipal solid waste; FW, food waste; MSW, municipal solid waste; STR, stirred tank reactor; UASB, upflow anaerobic sludge blanket; SBR, sequencing batch reactor.</p>
</fn>
<fn id="Tfn1">
<label>a</label>
<p>[ml-CH<sub>4</sub>/(g-TS)].</p>
</fn>
<fn id="Tfn2">
<label>b</label>
<p>[ml-CH<sub>4</sub>/(g-COD)].</p>
</fn>
<fn id="Tfn3">
<label>c</label>
<p>[g-COD/(L&#x2219;d)].</p>
</fn>
</table-wrap-foot>
</table-wrap>
</sec>
<sec id="s6">
<title>Effluent Recirculation in Multi-Stage AD</title>
<p>Effluents from each stage can be recirculated and added to every tank in phase-separated AD. Thus, high degradation rates can be achieved, when e.g. incompletely degraded substances from the methanogenesis undergo hydrolysis twice, enhancing energy recovery up to 9% in two-stage systems (<xref ref-type="bibr" rid="B24">Chatterjee and Mazumder, 2019</xref>). Previous work has reported the dilution of high solid feedstocks and pH control, achieved by recirculating the alkaline effluent obtained in the second stage, as main benefits in two-stage AD (<xref ref-type="bibr" rid="B125">Van et&#x20;al., 2020</xref>). In fact, this preserves nutrients and microorganisms in the system, allowing for the use of higher OLR, e.g. discussed by <xref ref-type="bibr" rid="B85">Menzel et&#x20;al. (2020)</xref>. By recirculating the liquid fraction of the AD effluent after solid-liquid separation, a wash out of fluidized microorganisms to the next stage will decrease. Thereby, the retention times of the microbes is elongated, which also improves process stability and performance, as observed by <xref ref-type="bibr" rid="B55">Jiraprasertwong et&#x20;al. (2018)</xref> in their three-stage AD system. Effluent recirculation can thus be used as a tool to stabilize and control AD processes, which is typically seen as a hurdle for their commercialization at large-scale. Recent studies have proven that recirculation strategies are indeed beneficial to increase process stability and performance for e.g., in the digestion of toxic citrus wastes, while increasing methane yields by 79% (<xref ref-type="bibr" rid="B131">Wikandari et&#x20;al., 2018</xref>). <xref ref-type="bibr" rid="B106">Qin et&#x20;al. (2019)</xref> have also reported more stability in the long-term operation of a two-phase process with effluent recirculation for the AD of food and paper waste. The study suggested that hydrogen-producers were recirculated to the first-stage after proliferation in the second stage, which contributed to the production of 79&#xa0;L-H<sub>2</sub>/kg-VS and 329&#xa0;L-CH<sub>4</sub>/kg-VS. <xref ref-type="bibr" rid="B129">Wang et&#x20;al. (2020)</xref> have also demonstrated an improved hydrogen and methane production resulting from effluent recirculation in their two-stage AD experiments using FW combined with cow dung, while additionally reducing the amount of alkali addition for pH control in the hydrogen-reactor. <xref ref-type="bibr" rid="B99">Paillet et&#x20;al. (2021)</xref> reported that the performance of hydrogen production from anaerobic OFMSW degradation could be improved by 330%, up to 17.2&#xa0;ml/g-VS, when applying a strategy based on effluent recirculation and systematic heat shock treatment. Compared to a single-stage reactor, <xref ref-type="bibr" rid="B34">Ding et&#x20;al. (2021)</xref> described an increased energy yield of 18% and a higher possible FW loading (up to 20% of the working volume), along with stable biogas production, in a FW-fed two-stage AD system with liquid recirculation from the methanogenic into the hydrolytic stage. The recirculation of the effluent from the second reactor also led to a higher robustness of the system against side effects through high OLR (e.g. acidification) compared to the single-stage application. Moreover, methane yields of nearly 400&#xa0;ml/g-VS, that is over 90% of the methane production potential, were reported. Recirculation of the liquid phase can stabilize the microbial consortium and adds another possibility for process control. <xref ref-type="bibr" rid="B133">Wu et&#x20;al. (2015)</xref> investigated the performance of two temperature-phased (thermophilic-mesophilic) double-STR digesters for the treatment of FW and compared it to a mesophilic single-stage application. In the two-stage digester without recirculation, the processes of hydrolysis and acidogenesis were inhibited by a pH drop below 4.0 in the first stage. Thus, the results for the methane production were very similar to the mono-digester, around 440 to 450&#xa0;ml-CH<sub>4</sub>/(g-VS). The methane ratio in the produced biogas from the second digester was 61% (<xref ref-type="bibr" rid="B133">Wu et&#x20;al., 2015</xref>). The two-stage AD application with recirculation from the second into the first stage achieved to keep the pH-value in the first digester at an optimal level of 5.0&#x2013;5.5. In consequence, the microorganisms in the first digester produced biogas with a hydrogen share of 30% (v/v). The portion of methane in the biogas rose to 70% (v/v). The particulate COD was reduced from 66.7% in the substrate to 10.3% (w/w) in the effluent. In comparison, in the single-stage digester and the two-stage AD application without recirculation, the COD remained at 14.6% (w/w).</p>
<p>Effluent recirculation in two-stage AD processes, however, must be carefully monitored and controlled, as methane production may be favored at a pH-value that is higher than 6.0, hindering biohydrogen production (<xref ref-type="bibr" rid="B87">Micolucci and Uellendhal, 2018</xref>). This issue is avoided in three-stage AD systems with separated hydrolysis and acidogenesis, as the recirculation of methanogenic sludge into the first stage does not interfere with hydrogen synthesis in the acidogenic reactor (<xref ref-type="bibr" rid="B55">Jiraprasertwong et&#x20;al., 2018</xref>).</p>
</sec>
<sec id="s7">
<title>Monitoring and Control</title>
<p>A reliable monitoring and control system is a pre-requisite for phase separation in AD. A suitable monitoring system is required to orchestrate the exchange of the gas, and in particular the liquid phase in between the stages to prevent cell starvation or product inhibition.</p>
<p>Sensors for AD need a resistance against chemical and physical conditions like low pH-values and an undefined multiple-component matrix in the broth (<xref ref-type="bibr" rid="B15">Bockisch et&#x20;al., 2019</xref>). Naturally, an important process parameter for AD is the pH-value. The response time of the system&#x2019;s pH-value to changing conditions inside is not by all means very fast due to the buffer capacity of the broth (<xref ref-type="bibr" rid="B70">Li et&#x20;al., 2014</xref>). An accumulation of acids inside a tank does not necessarily mean an immediate decrease of the pH-value. Any drop in the pH-value exhibits severe imbalances, which cannot be rapidly counteracted and typically need several days or even weeks to recover (<xref ref-type="bibr" rid="B104">Pfeiffer et&#x20;al., 2020</xref>). In that case, the OLR has to be decreased significantly, even the addition of anti-foam agents might be needed due to increased cell lysis rates and protein excretion (<xref ref-type="bibr" rid="B88">Moeller and Zehnsdorf, 2016</xref>). Controlling the pH-value, however, is the most suitable tool for separating the different groups of microorganisms between the reactors of multi-stage AD. At a low pH-value of between 5.0 and 6.0, the presence of methanogens in the acidogenic phase is prevented. The pH-value can be measured with on line monitoring methods like classical voltametric pH electrodes (AgCl), fluorescence based sensors or ion selective field effect transistors (<xref ref-type="bibr" rid="B54">Jimenez-Jorquera et&#x20;al., 2010</xref>; <xref ref-type="bibr" rid="B14">Bockisch et&#x20;al., 2014</xref>; <xref ref-type="bibr" rid="B52">Janzen et&#x20;al., 2015</xref>). Fluctuations of the pH-value caused by an organic overload of the AD system can be corrected by reducing the substrate feed. Acidified digesters can be treated additionally with sodium bicarbonate in a bypass or between the stages of multi-stage AD to rise the pH-value (<xref ref-type="bibr" rid="B18">Burgstaler et&#x20;al., 2010</xref>).</p>
<p>For all AD applications, especially for FW-treating digesters, the amount of produced SCCAs is a proper parameter to observe the process functionality (<xref ref-type="bibr" rid="B104">Pfeiffer et&#x20;al., 2020</xref>). An adequate amount of the effluent from the acidogenesis needs to be transferred to the second (or third) stage in order to prevent starvation in the methanogenic stage without the risk of its acidification. SCCAs can be monitored on- and off line with near or mid-wavelength infrared spectroscopy sensors (<xref ref-type="bibr" rid="B37">Falk et&#x20;al., 2015</xref>; <xref ref-type="bibr" rid="B94">Nespeca et&#x20;al., 2017</xref>). Infrared spectroscopy (<xref ref-type="bibr" rid="B94">Nespeca et&#x20;al., 2017</xref>) or gas chromatography for the detection of volatile compounds (<xref ref-type="bibr" rid="B143">Zheng et&#x20;al., 2020</xref>) has proven to be a suitable strategy for identifying concentration changes of acids in a short time scale (<xref ref-type="bibr" rid="B11">Bj&#xf6;rnsson et&#x20;al., 2001</xref>), however this is rarely applied in practice so&#x20;far.</p>
<p>Alkalinity is also considered as an early-warning indicator that can effectively predict disturbances in AD processes. Several studies have demonstrated that enhanced SCCA production could be obtained from sewage sludge under alkaline conditions, typically using NaOH to maintain pH values around 10 (<xref ref-type="bibr" rid="B67">Kurahashi et&#x20;al., 2017</xref>; <xref ref-type="bibr" rid="B78">Liu et&#x20;al., 2018</xref>). Controlled alkalinity at a pH in the range of between 10 and 11 during the AD of sewage sludge in a full-scale reactor (30&#xa0;m&#xb3;) inhibited methane production, while enhancing SCCA accumulation, particularly acetic acid which accounted for 58% (w/w) of the total SCCAs (<xref ref-type="bibr" rid="B78">Liu et&#x20;al., 2018</xref>). A thorough review about process stability for AD of FW has suggested that a ratio of intermediate to partial alkalinity (IA/PA) lower or equal to 0.3 should be used, along with total alkalinity (TA) concentrations of between 13 and 15&#xa0;g/L (<xref ref-type="bibr" rid="B73">Li et&#x20;al., 2018</xref>). Despite the proposed thresholds, these depend on substrate quality and the type of operation, and are less reliable under variable feedstock or operating conditions (<xref ref-type="bibr" rid="B135">Wu et&#x20;al., 2019</xref>).</p>
<p>Cell polarizability measurements can provide a value that reflects the metabolic activity of cells that is related to cell physiology. This is especially helpful if different consortia exist in multiple stages while the measurement of intermediates, and thus the production rates, is not easily feasible or cell stress that usually leads to a reduction of the polarizability, shall be prevented quickly. This can be starvation due to a lack of nutrient supply or an oversupply of nutrients. Frequency-dispersed anisotropic polarizability (FDAP) can be used as an at-line control to evaluate cell viability and activity in each stage. Such electrooptical measurements have been successfully used to monitor DF using mixed cultures (<xref ref-type="bibr" rid="B46">G&#xf3;mez-Camacho et&#x20;al., 2020</xref>), which exposes a different metabolic activity on the dependence of acid accumulation. The same study also revealed the suitability of flow cytometry for DF cultures, in which a typical live-dead staining can be conducted, which is otherwise difficult in cultures of one-stage AD, probably due to agglomerate formation between acidogens and methanogens.</p>
<p>Ammonia acts as an inhibitor for specific enzymatic reactions. It has been shown previously that biogas plants suffer from microbial inhibition and methane losses when using N-rich substrates (<xref ref-type="bibr" rid="B90">Morozova et&#x20;al., 2020</xref>). While concentrations above 200&#xa0;mg/L are considered to hinder AD significantly, according to <xref ref-type="bibr" rid="B25">Chen et&#x20;al. (2008)</xref>, lower amounts are beneficial for stabilizing AD processes, by buffering the system (<xref ref-type="bibr" rid="B95">Nsair et&#x20;al., 2020</xref>). Ammonia concentrations of 14&#xa0;mg/L can already have an impact on methane production, as described by <xref ref-type="bibr" rid="B95">Nsair et&#x20;al. (2020)</xref>. Therefore, in multi-stage AD applications, the monitoring of ammonia concentrations has a particular importance for the methanogenic stage. Ammonia can be measured with potentiometric sensors, electronic tongues or luminescent ammonia sensors (<xref ref-type="bibr" rid="B93">Nery and Kubota, 2016</xref>; <xref ref-type="bibr" rid="B124">Urriza-Arsuaga et&#x20;al., 2019</xref>). A study comparing off line and on line measurements concluded that the NH<sub>4</sub> electrode had high accuracy, but was strongly affected by sodium and potassium, so that it was not of an equal accuracy (<xref ref-type="bibr" rid="B144">Zhou and Boyd, 2016</xref>). The performance of AD can also benefit from a microbial adaptation, e.g. through a gradually N-increasing feeding rate, in which the viability and activity of the microbial community is investigated (<xref ref-type="bibr" rid="B90">Morozova et&#x20;al., 2020</xref>). An issue remains for measurements at the typically high concentrations above 50&#xa0;mg/L, which hinders often on line applications as it is not easily feasible to dilute the broth in an automatic&#x20;manor.</p>
<p>In order to use the hydrogenotrophic methane production pathway, methanogenic archaea are dependent on dissolved hydrogen in the liquid phase of an AD application. The hydrogen solubility in water is low. At 25&#xb0;C and a pressure of 1 bar, hydrogen saturated water contains 1.6&#xa0;mg hydrogen/L (<xref ref-type="bibr" rid="B59">Kaye and Laby, 1992</xref>). Nevertheless, an accumulation of hydrogen during AD can inhibit the growth of certain acidogenic bacteria (e.g. <italic>Clostridium</italic>). While the threshold depends on the microbial consortia, hydrogen partial pressures above 10<sup>&#x2013;5</sup> to 10<sup>&#x2013;3</sup> bar are described as having negative effects, especially on butyrate and propionate degradation (<xref ref-type="bibr" rid="B80">Lowe et&#x20;al., 1993</xref>; <xref ref-type="bibr" rid="B92">Mutungwazi et&#x20;al., 2021</xref>). In the worst case, this can lead to a collapse of the AD system and the biogas production through acidification (<xref ref-type="bibr" rid="B50">Huck et&#x20;al., 2013</xref>).</p>
<p>In multi-stage AD, the interspecies-hydrogen transfer between acidogens and methanogens is interrupted due to their spatial separation. The phase-transfer from gas to liquid can thus act as the bottleneck of methanation (<xref ref-type="bibr" rid="B33">D&#xed;az et&#x20;al., 2020</xref>). Monitoring of the process stability simply by observing the gas phase may result in problems like reactor overloads, as the reaction to system changes in the headspace tends to be slow compared to the response in the liquid phase (<xref ref-type="bibr" rid="B10">Bj&#xf6;rnsson et&#x20;al., 2000</xref>). <xref ref-type="bibr" rid="B11">Bj&#xf6;rnsson et&#x20;al. (2001)</xref> showed, that the dissolved hydrogen concentration reacts faster to changes in OLR or other system fluctuations, for example the accumulation of SCCAs. In their experiments, the authors used an on-line Teflon membrane for sampling, combined with a semiconductor sensor, which is highly hydrogen specific (<xref ref-type="bibr" rid="B11">Bj&#xf6;rnsson et&#x20;al., 2001</xref>).</p>
<p>Acetogenic bacteria are highly dependent on the hydrogen uptake by the archaea, as the accumulation of dissolved hydrogen leads the inhibition of their degradation of SSCA like butyrate and propionate (<xref ref-type="bibr" rid="B48">Harper and Pohland, 1986</xref>). In consequence, these acids can be enriched and cause further system instabilities. It was shown that ethanol accumulated up to 0.08&#xa0;g/L under a hydrogen headspace pressure of 2&#x20;bar during anaerobic digestion. The profile of acids was partially altered (<xref ref-type="bibr" rid="B115">Sarkar et&#x20;al., 2017</xref>). This example demonstrates that hydrogen plays a crucial regulatory role in acidogenesis and acetogenesis; a partial pressure of hydrogen below 10<sup>&#x2013;4</sup> bar is required to maintain the thermodynamical feasibility of the acid synthesis (<xref ref-type="bibr" rid="B102">Pavlostathis, 2011</xref>). Thus, the monitoring of the dissolved hydrogen shows, if the different groups of microorganisms act at equilibrium (<xref ref-type="bibr" rid="B11">Bj&#xf6;rnsson et&#x20;al., 2001</xref>). The monitoring of dissolved hydrogen is typically coupled to the use of membranes in order to increase the hydrogen selectivity of a measurement unit. These membranes tend to be overgrown by microbial communities and their biofilms in AD applications. Researchers at the Kurt-Schwabe-Institute (Meinsberg, Germany) are developing a new approach for the on-line measurement of dissolved hydrogen based on the potentiostatic coulometry. The system relies on a gas-liquid extraction without membranes (<xref ref-type="bibr" rid="B145">Zosel et&#x20;al., 2011</xref>). Optimization work for the application in AD is ongoing.</p>
</sec>
<sec id="s8">
<title>Biological Methanation of Hydrogen</title>
<p>Demand-oriented energy production is a main issue in a sustainable society, which relies on fluctuating energy resources. During the ongoing transformation of the energy supply systems, a temporary surplus or shortage of electrical power occurs with the necessary expansion of renewable resources like wind and solar power (<xref ref-type="bibr" rid="B117">Sensfuss and Pfluger, 2014</xref>; <xref ref-type="bibr" rid="B103">Peters et&#x20;al., 2018</xref>). For instance, feed-in management measures led to the curtailment of 5.4&#xa0;TWh from renewables in Germany in 2018, 97% of it originated from wind plants (<xref ref-type="bibr" rid="B17">Bundesnetzagentur, 2019</xref>). Energy curtailment created costs of 1.5 billion Euro to Germany&#x2019;s electricity consumers in 2017 (<xref ref-type="bibr" rid="B51">International Energy Agency, 2020</xref>). Flexible biogas production has the potential to partly buffer this residual load in rural areas up to a certain degree (<xref ref-type="bibr" rid="B68">Lecker et&#x20;al., 2017</xref>). In recent years, the concept of power-to-gas has gained a broad interest (<xref ref-type="bibr" rid="B103">Peters et&#x20;al., 2018</xref>). Surpluses of electrical energy from renewable sources can be used to produce hydrogen from water by electrolysis. In combination with carbon dioxide, this hydrogen can react chemically to methane through the Sabatier reaction (<xref ref-type="bibr" rid="B68">Lecker et&#x20;al., 2017</xref>; <xref ref-type="bibr" rid="B108">Rachbauer et&#x20;al., 2017</xref>).<disp-formula id="equ1">
<mml:math id="m1">
<mml:mrow>
<mml:mi>C</mml:mi>
<mml:msub>
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<mml:mn>2</mml:mn>
</mml:msub>
<mml:mo>&#x2b;</mml:mo>
<mml:mn>4</mml:mn>
<mml:msub>
<mml:mi>H</mml:mi>
<mml:mn>2</mml:mn>
</mml:msub>
<mml:mo>&#x2192;</mml:mo>
<mml:mi>C</mml:mi>
<mml:msub>
<mml:mi>H</mml:mi>
<mml:mn>4</mml:mn>
</mml:msub>
<mml:mo>&#x2b;</mml:mo>
<mml:mn>2</mml:mn>
<mml:msub>
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</disp-formula>
</p>
<p>This process is called chemical methanation. To store the chemical energy as gas withing the gas distribution grid is much easier compared to storing electricity. The German gas grid, for example, can store up to 260&#xa0;TWh of energy on its own (<xref ref-type="bibr" rid="B68">Lecker et&#x20;al., 2017</xref>).</p>
<p>In biogas reactors, hydrogenotrophic methanogens (archaea) like <italic>methanococcales</italic> or <italic>methanobacterium</italic> convert hydrogen into methane through the Sabatier reaction (<xref ref-type="bibr" rid="B6">Bassani et&#x20;al., 2015</xref>; <xref ref-type="bibr" rid="B108">Rachbauer et&#x20;al., 2017</xref>). The hydrogen for biological methanation originate from the electrolysis of water, the required carbon dioxide can be taken from the AD process (<xref ref-type="bibr" rid="B103">Peters et&#x20;al., 2018</xref>). Thus, the concept is suited for a multi-stage AD: the first stage provides the necessary carbon dioxide for the methanation and simultaneously provide SCCAs as a carbon source for archaea. With the lack of intermediates from fermentative bacteria, a single-stage methanation would have to rely on an additional supply with organic carbon and different trace elements.</p>
<p>Through the addition of hydrogen to AD applications, hydrogenotrophic methanogenesis is amplified and a shift in consortia of methanogenic archaea is observable (<xref ref-type="bibr" rid="B108">Rachbauer et&#x20;al., 2017</xref>; <xref ref-type="bibr" rid="B97">Okoro-Shekwaga et&#x20;al., 2019</xref>). A higher quantity of hydrogenotrophic methanogens leads to a higher quality of the biogas due to the exhaustion of the carbon dioxide, e.g. originating from the previous AD processes, during methanogenesis. Therefore, a utilization of external hydrogen in biogas plants can decrease the costs for the enrichment of biogas, if used as biomethane (<xref ref-type="bibr" rid="B68">Lecker et&#x20;al., 2017</xref>).</p>
<p>Hydrogenotrophic methanogenesis in multi-stage AD with addition of hydrogen has been investigated by several researchers. <xref ref-type="bibr" rid="B6">Bassani et&#x20;al. (2015)</xref> described that hydrogen addition to a two-stage AD-reactor (STR) fed with cattle manure increased the content of methane in the biogas from 70% to nearly 90% (v/v) under mesophilic conditions through hydrogen inflow. The HRT was 25&#xa0;days in the first and 33&#xa0;days in the second reactor, with a total OLR of 0.6&#xa0;g-VS/(L&#x2219;d). The hydrogen was added to the second reactor through a diffuser at a rate of 192&#xa0;ml/(L&#x2219;d), to meet the stoichiometric needs for methanation (four moles of hydrogen per mole of carbon dioxide). Similar results were achieved by <xref ref-type="bibr" rid="B81">Luo et&#x20;al. (2012)</xref>. The authors demonstrated that the methane production rate of a cattle manure (3% (w/w) of TS, of which 2.6% VS) increased more than 20% due to the continuous addition of hydrogen. According to <xref ref-type="bibr" rid="B103">Peters et&#x20;al. (2018)</xref>, the methane fraction in the biogas can achieve up to 95% through hydrogenotrophic methanogenesis. Km values of anaerobic cell suspensions are in the range of between 5 and 10&#xa0;&#xb5;M (<xref ref-type="bibr" rid="B112">Robinson and Tiedje, 1982</xref>). The addition of hydrogen to AD applications results in a rising partial pressure, which can even lead to inhibition as described in a previous section. If it is converted fast enough, it creates no change in substrate consumption though as shown by <xref ref-type="bibr" rid="B146">Luo and Angelidaki (2013)</xref>. The possibilities of biogas upgrading by pulse hydrogen addition to AD fed with straw and sludge from a biogas plant&#x20;was investigated by <xref ref-type="bibr" rid="B2">Agneessens et&#x20;al. (2017)</xref>. An OLR of 0.77&#xa0;g-VS/(L&#x2219;d) and a HRT of 20&#xa0;days were chosen as process conditions. The experiments showed a fast adaption and hydrogen assimilation of the microbial community, an increase of hydrogenotrophic methanogens as <italic>Methanobacterium</italic> was detected. The methane production (up to 0.44&#xa0;L/(L&#x2219;d)) was reduced at a carbon dioxide gas concentration below 12% (v/v) (<xref ref-type="bibr" rid="B2">Agneessens et&#x20;al., 2017</xref>), which shows the importance to maintain a sufficient availability to restrict it to become rate limiting.</p>
<p>
<italic>Methanobacterium</italic> was one of the prevalent archaea found by <xref ref-type="bibr" rid="B72">Li et&#x20;al. (2020)</xref> on the conversion of hydrogen to methane in a two-stage anaerobic digester fed with rice-straw. It was possible to increase the methane yield (by 45%) and the methane share in the biogas (by 101%) through addition of hydrogen to a STR - up-flow reactor combination (<xref ref-type="bibr" rid="B72">Li et&#x20;al., 2020</xref>). The concept of hydrogen addition to upgrade the produced biogas was also investigated in a two-stage thermophilic reactor (STR and up-flow reactor) digesting cattle manure and potato-starch by <xref ref-type="bibr" rid="B29">Corbellini et&#x20;al. (2018)</xref>. The hydrogen was injected in the first reactor and channeled to the second one, together with the off-gas. 98% of the hydrogen was metabolized into methane.</p>
<p>Within the large group of methanogenic archaea, countless numbers of species exist. Some of these species are especially persistent against the stress caused by the process conditions inside of an AD reactor or the chemical substances inflowing with the feed. The concept of enriching exactly these microorganisms with bioaugmentation is used since nearly 20&#xa0;yr (<xref ref-type="bibr" rid="B96">Nzila, 2017</xref>). The concept is especially suitable for multi-stage AD, where the different organism groups can be augmented more individually. It was observed by <xref ref-type="bibr" rid="B1">&#xc1;cs et&#x20;al. (2019)</xref>, as they changed the conditions inside a mesophilic lab-scale reactor, inoculated with the effluent of an industrial biogas plant (for pig manure and plant silage), to those of a power-to-methane system, by sole hydrogen feeding. The diversity of the archaea community was significantly reduced, while <italic>Methanobacterium</italic> remained the predominant genus (<xref ref-type="bibr" rid="B1">&#xc1;cs et&#x20;al., 2019</xref>). <xref ref-type="bibr" rid="B140">Zhang et&#x20;al. (2018)</xref> described an example of how to use syntrophic relationships of anaerobic digesters in combination with bioaugmentation. They added exoelectrogenic <italic>Geobacter sulfurreducens</italic> to a batch culture of methanogens. <italic>Methanosaetaceae</italic> and <italic>Methanobacteriaceae</italic> benefited strongly from the augmentation, as they occurred in direct vicinity of the new species. With this new bioaugmentation strategy, the methane production rate was increased by nearly 80%. A rearrangement of the methanogenic consortium inside an AD application is especially helpful for the treatment of nutrient-poor substrates, or those which have a high amount of inhibitors like ammonia, as seen by the experimental results from <xref ref-type="bibr" rid="B75">Li Y. et&#x20;al. (2018)</xref> and <xref ref-type="bibr" rid="B40">Fotidis et&#x20;al. (2017)</xref>.</p>
<p>An alternative to the direct addition of hydrogen to full AD is a single methanogenic stage or bio-electrochemical methanogenesis, which could benefit from carbon dioxide supply of other AD stages, but would be operated separately from the broth streams. The utilization of power-to-gas has also been examined for bio-electro-methanogenesis with pure or mixed methanogenic cultures, combining electrochemical operation with microbial conversion to produce methane from carbon dioxide. Cathodes inside the bioreactors act as electron donators for the methanogenic reduction of carbon dioxide or as <italic>in-situ</italic> hydrogen producers (<xref ref-type="bibr" rid="B42">Geppert et&#x20;al., 2019</xref>; <xref ref-type="bibr" rid="B65">Kracke et&#x20;al., 2019</xref>). <italic>In-situ</italic> hydrogen production in bio-electrochemical methanogenesis offer a flexibilization of energy production through power-to-gas applications, as they can be used with single-stage, pure methanogenic species in defined cultures and without external hydrogen supply. <xref ref-type="bibr" rid="B66">Kracke et&#x20;al. (2020)</xref> investigated the power-to-gas electromethanogenesis of <italic>Methanococcus maripaludis</italic> in stirred bio-electrochemical reactors. Carbon dioxide for the biological methanation was continuously added. Volumetric methane production rates of nearly 1.4&#xa0;L/(L&#x2219;d) were achieved. The methanogens, that were exposed to cathodes showed slightly higher metabolization efficiency than a control group, which was supplied with external hydrogen. The efficiency of <italic>Methanococcus maripaludis</italic> in terms of electro-methanogenesis was confirmed by <xref ref-type="bibr" rid="B83">Mayer et&#x20;al. (2019)</xref>, who compared the electrosynthesis of methane of different archaea strains in a fed-batch, two-chamber pilot-scale reactor (H-cell), and by <xref ref-type="bibr" rid="B35">Enzmann et&#x20;al. (2019)</xref>, using carbon dioxide fed bubble columns with carbon layer cathodes. <xref ref-type="bibr" rid="B64">Kobayashi et&#x20;al. (2017)</xref> used a thermophilic (55&#xb0;C), high-pressure system with a mixed culture of methanogens for the bio-electrochemical synthesis of methane. The archaea in the system were dominated by <italic>Methanothermobacter</italic> (<xref ref-type="bibr" rid="B64">Kobayashi et&#x20;al., 2017</xref>). At even higher temperatures (60&#xb0;C), but with atmospheric pressure, <xref ref-type="bibr" rid="B119">Song et&#x20;al. (2019)</xref> did similar experiments with a mixed culture of methanogens.</p>
<p>The overall efficiency of a process nexus (electrolysis, methanation and conversion into usable energy) is barely above 50%, depending on the pressure and the temperature (<xref ref-type="bibr" rid="B8">Bernacchi et&#x20;al., 2014</xref>). Nevertheless, the conversion of hydrogen into methane represents a promising technology for the prospective increase of energy supply from fluctuating sources. While this concept can be implemented directly into existing digestion processes, research results exist only from pilot scale applications yet and therefore need further investigation on the large scale (<xref ref-type="bibr" rid="B68">Lecker et&#x20;al., 2017</xref>; <xref ref-type="bibr" rid="B122">Theuerl et&#x20;al., 2019</xref>).</p>
</sec>
<sec id="s9">
<title>Modelling of Multi-Stage AD Processes</title>
<p>Mathematical models are an important tool to understand and predict the degradation processes in AD. They are especially helpful for designing and operating multi-stage reactor concepts, as they estimate the flow rates between and feeding rates of the individual stages. Naturally, first mechanistic models were obviously established for single-stage AD processes. <xref ref-type="bibr" rid="B13">Blumensaat and Keller (2005)</xref> adapted the &#x201c;Anaerobic Digestion Model No. 1 (ADM1)&#x201d; to a two-stage AD process. The authors were able to predict the process performances of both stages individually. <xref ref-type="bibr" rid="B91">Muha et&#x20;al. (2013)</xref>, simulated the share of reactions in a leach bed reactor and an anaerobic filter. According to the model, all steps of AD took place in both reactors except for the hydrolysis: about 40% of the acidogenesis and nearly 75% of the methanogenesis occurred in the second stage. <xref ref-type="bibr" rid="B126">Vega De Lille et&#x20;al. (2016)</xref> were able to predict the COD course from domestic wastewater in a two-stage AD system, consisting of a sequencing batch reactor and a fixed bed reactor. The authors used an adjusted ADM1, which showed good results for the degradation of varying feedstock. <xref ref-type="bibr" rid="B58">Kamyab and Zilouei (2021)</xref> simulated the biogas production from a two-stage mixed UASB reactor for the treatment of baker&#x2019;s yeast wastewater. It predicted, that the efficiency of the COD removal rises from 11 to 36% with an increased input concentration between 1.5 and 4.1&#xa0;mg-COD/cm&#xb3;. Simultaneously, the methane production rate decreases from 1.2&#xa0;L/g-COD at 1.5&#xa0;mg-COD/cm&#xb3; to almost zero at 4.1&#xa0;mg-COD/cm&#xb3;. <xref ref-type="bibr" rid="B7">Bayen and Gajardo (2019)</xref> used the anaerobic digestion model AM2 for simulating biogas production it in a two-stage system consisting of a separate acidogenic and methanogenic stage. The model expressed the optimal flow rates within the system, e.g. for the treatment of a substrate with a high release of SCCAs.</p>
<p>Mathematical models for AD are often developed for a certain scope of application. Therefore it can be useful to adapt models from a different application for one or all stages of AD, as described by <xref ref-type="bibr" rid="B105">Postawa (2018)</xref>. He used a model originally designed for high pressure AD, to predict the biogas production in a temperature phased two-stage AD and compared the results with literature data. While not fully optimised, the model predicted the biogas production well for time periods of 40&#xa0;days in AD. The recent results from the modelling of multi-stage AD processes show that stage separation becomes predictable. It might be even easier to simulate separate stages as the number of parallel reactions and influencing factors is reduced. If sufficient data under dynamic operation is available, either the production dynamics can be predicted or process disturbances can be identified with suitable monitoring tools. On a system level, the potential yields and value generation can be simulated.</p>
</sec>
<sec id="s10">
<title>Economic Competitiveness and Alternative Products</title>
<p>Due to the higher investment and operational costs, and although promising as described previously, multi-stage digesters cannot compete economically for all types of feedstock. The investment costs for single- and two-stage biogas plants with a capacity of 100&#xa0;kW have been estimated as 7000&#x20;&#x20ac;/kW (<xref ref-type="bibr" rid="B19">Carlini et&#x20;al., 2017</xref>) and 7400&#x20;&#x20ac;/kW (<xref ref-type="bibr" rid="B111">Renda et&#x20;al., 2016</xref>), respectively. Organic waste residues with a dry matter content below 3% like sewage sludge exhibit similar methane yields (0.5&#xa0;L/(L<sub>digestate</sub>&#x2219;d) when treated either in single-stage AD (STR) or two-stage processes (<xref ref-type="bibr" rid="B116">Schievano et&#x20;al., 2012</xref>; <xref ref-type="bibr" rid="B125">Van et&#x20;al., 2020</xref>). For the transfer between the stages of AD, a sufficient mixing is a premise. Thus, multi-stage AD is typically operated with STRs. Feedstock with a high TS-content (&#x3e;15&#x2013;20%) is difficult to apply in these reactors due to the high viscosity (<xref ref-type="bibr" rid="B125">Van et&#x20;al., 2020</xref>). According to this study, great amounts of water and energy as well as long HRT are needed to treat such feedstock in two-stage digesters. Therefore, dry single-stage digesters are recommended in this&#x20;case.</p>
<p>Beside the benefits for biogas production, phase separation in AD allows the recovery of value-added side products from some of the stages, e.g. from DF. Two-stage AD processes for the combined production of biohydrogen and biomethane from organic wastes can yield a biohythane gas containing 10&#x2013;15% H<sub>2</sub>, 50&#x2013;55% CH<sub>4</sub>, and 30&#x2013;40% CO<sub>2</sub>. The upgrade of the SCCA-enriched liquid effluent generated in the first stage can lead to higher energy recovery and higher degradation efficiency than in traditional biogas production processes (<xref ref-type="bibr" rid="B98">O-Thong, 2018</xref>). <xref ref-type="bibr" rid="B72">Li et&#x20;al. (2020)</xref> tested a semi-continuous two-stage AD system for biohythane production from cornstalk. The hydrogen production in the first-stage reached 25&#xa0;ml/g-TS, the hydrogen content in the biohythane gas was 18.47%. In the second stage UASB, a methane yield of 95&#xa0;ml/g-TS was additionally achieved by using the liquid effluent generated in the first stage. <xref ref-type="bibr" rid="B44">Ghimire et&#x20;al. (2020)</xref> investigated the role of temperature in a two-stage DF and AD process using FW, and observed that mesophilic (34&#xb0;C) DF provided a hydrogen yield of 53.5&#xa0;ml H<sub>2</sub>/g-VS, while thermophilic conditions (55&#xb0;C) favored methane yields in AD, achieving 307.5&#xa0;ml CH<sub>4</sub>/g-VS. <xref ref-type="bibr" rid="B136">Yan et&#x20;al. (2020)</xref> assessed the performance of a two-stage system using leach bed reactors for the AD of several types of FW, and achieved a hydrogen production of 61&#xa0;ml/g-VS. By applying the produced leachate and acidogenic off-gas in the second stage, the authors reached a methane production of 420&#xa0;ml/g-VS. <xref ref-type="bibr" rid="B27">Chen et&#x20;al. (2021)</xref> used a temperature phased AD of rice straw and pig manure for biohythane production. In a mesophilic-thermophilic reactor concept, up to 16.7&#xa0;ml-H<sub>2</sub>/g-VS and 197.7&#xa0;ml-CH<sub>4</sub>/g-VS were measured, which implies a ratio of 1&#xa0;ml H<sub>2</sub> per 12&#xa0;ml&#x20;CH<sub>4</sub>.</p>
<p>Based on the DF of several biodegradable wastes, it is estimated that two-thirds of the carbon input can be fermented into SCCAs such as acetic, propionic, butyric, isovaleric, valeric and caproic acid, among others (<xref ref-type="bibr" rid="B118">Slezak et&#x20;al., 2017</xref>). Although extensive reviews exist on the topic, SCCAs production <italic>via</italic> AD is sensitive to several operational factors, namely feedstock, pH-value, temperature, organic loading rate, alkalinity, and retention time, respectively, which typically depict a synergetic effect on the microbial consortia (<xref ref-type="bibr" rid="B4">Atasoy et&#x20;al., 2018</xref>). Before SCCAs gain an economic value during AD, they have to be concentrated and separated from the effluent (<xref ref-type="bibr" rid="B63">Kleerebezem et&#x20;al., 2015</xref>). <xref ref-type="bibr" rid="B45">Gioannis et&#x20;al. (2017)</xref> described the production of SCCAs in a single- and two-stage FW-fed STR. SCCAs concentrations of 5&#xa0;g/L were detected in the acidogenesis stage. Bioaugmentation has been successfully applied to enhance SCCAs production, increasing butyric and caproic acid yields by up to 300% with <italic>Clostridia</italic>, <italic>Sphingobacteriales</italic>, <italic>Desulfobacteraceae</italic> and <italic>Bacillus</italic> species (<xref ref-type="bibr" rid="B110">Reddy et&#x20;al., 2018</xref>). Further investigation is required to maximize acid concentration while keeping the microbial consortia vital and eventually combine the concomitant biomass growth with the enrichment of species that have a high value as fertilizer, e.g. for soil recovery or as biofungicide producers like <italic>Bacillus</italic>&#x20;sp.</p>
</sec>
<sec sec-type="conclusion" id="s11">
<title>Conclusion</title>
<p>Phase separation in AD provides a great potential for the flexibilization of AD applications, which is beneficial for a demand-driven biogas production. With more research on up-scaling, this approach is likely to be become applicable while using similar infrastructure as conventional AD processes.</p>
<p>Monitoring concepts coupled with dynamic effluent recirculation as also discussed in this work, allow for an increasing system robustness and stability. A robust and stable system also facilitates the use of feeding strategies with alternating feedstock, making it possible to integrate AD into regional material cycles. Strategies such as bioaugmentation help the adaptation of microbial communities that are most suitable for the conditions and requirements of the specific AD application.</p>
<p>Finally, additional benefits from the separation of SCCAs between stages of a multi-phase AD can couple biomass energy and material use. As one example, among others, the use of SCCAs as feed for the production of long-chain polyunsaturated fatty acids in subsequent microalgae mono-cultivation processes shall be mentioned (<xref ref-type="bibr" rid="B22">Chalima et&#x20;al., 2020</xref>; <xref ref-type="bibr" rid="B101">Patel et&#x20;al., 2021</xref>). They have a high value in nutrition and serve as a replacement of fish oil and fish meal. Such a process can, beside the value addition, represent a more sustainable production of these compounds for food and feed application (<xref ref-type="bibr" rid="B5">Bartek et&#x20;al., 2021</xref>). Nevertheless, research and development to increase the cost-efficiency of coupled systems and reduce efforts for separation is a pre-requisite so that such process combinations will be applied in industrial scale. Finally, data for techno-economic and sustainability assessments are required to identify suitable feedstock-product combinations within the manyfold options that a multi-stage AD theoretically offers to its&#x20;users.</p>
</sec>
</body>
<back>
<sec id="s12">
<title>Author Contributions</title>
<p>EJ collected data, performed literature research, and wrote the main body of the manuscript. JP supported data collection and manuscript preparation and review. PN supported supervision of the manuscript preparation and review. SJ supported data collection, supervised manuscript preparation and review.</p>
</sec>
<sec id="s13">
<title>Funding</title>
<p>The authors acknowledge funding of the German Federal Ministry for Economics within the framework program Biomass energy use, grant no. 03EI5409A.</p>
</sec>
<sec sec-type="COI-statement" id="s14">
<title>Conflict of Interest</title>
<p>The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.</p>
</sec>
<sec id="s15" sec-type="disclaimer">
<title>Publisher&#x2019;s Note</title>
<p>All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.</p>
</sec>
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<surname>Oel&#xdf;ner</surname>
<given-names>W.</given-names>
</name>
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<surname>Zimmermann</surname>
<given-names>P.</given-names>
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</person-group> (<year>2011</year>). <source>Final Report of the Joint Project: Process Optimization of Biogas Production by Means of Innovative Measuring and Control Technology for the Detection of Dissolved Hydrogen as a Microbial Key Intermediat (BINERWA)</source>. <comment>Available at: <ext-link ext-link-type="uri" xlink:href="https://www.fnr-server.de/ftp/pdf/berichte/22009407.pdf">https://www.fnr-server.de/ftp/pdf/berichte/22009407.pdf</ext-link> (Accessed April 8, 2021)</comment>.</citation>
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</article>