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BR Aguglia 2017
BR Aguglia 2017
Review
PII: S0960-8524(17)31049-0
DOI: http://dx.doi.org/10.1016/j.biortech.2017.06.145
Reference: BITE 18382
Please cite this article as: Braguglia, C.M., Gallipoli, A., Gianico, A., Pagliaccia, P., Anaerobic bioconversion of
food waste into energy: A critical review, Bioresource Technology (2017), doi: http://dx.doi.org/10.1016/j.biortech.
2017.06.145
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Anaerobic bioconversion of food waste into energy: a critical review
Camilla M. Braguglia*,braguglia@irsa.cnr.it, Agata Gallipoli, Andrea Gianico, Pamela
Pagliaccia
Istituto di Ricerca sulle Acque (IRSA-CNR), Area della Ricerca RM1, Via Salaria km
29,300 (00015 Monterotondo), Italy
*Corresponding author.
1. Introduction
Food waste was defined by the UN Food and Agriculture Organization (FAO) and
includes any healthy or edible substance that is wasted, lost, degraded at every stage of
the food supply chain. Every year, between 1.3 and 1.6 billion tons of food, such as
fresh vegetables, fruit, and meat, bakery and dairy products, are lost along the food-
supply chain, and this accounts for one third of the food produced globally for human
consumption, affecting several natural resources. Food waste, in fact, cost the global
economy around USD 990 billion annually, and consumes in fact about a quarter of all
the water used for agriculture purposes, and is responsible for an estimated 8 % of total
and rising living standards. Globally, around 2 billion tons of municipal solid waste are
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OFMSW), mainly food waste which collected from households, and restaurants, but the
composition may vary from country to country. The total FW quantity produced each
year in Europe has been estimated to be around 90 million tons Mt in 2012, of which an
per capita yearly against the 62 kg per capita per year wasted in Italy. Annually, in the
United States the amount of food wasted is nearly 61 Mt, in South Korea around 6.2 Mt
and in China, despite the low food waste per capita (55 kg annually), is 195 Mt. The EU
mainly due to increased FW generation in households, that almost doubled from 2004 to
2012, while FW from food manufacturing and agriculture showed decreasing trend. The
composition of the food wasted at household and food service level (restaurants,
canteen, etc.) varies from region to region in the world. In fact, as showed in Figure 1,
in Europe, FW is composed by 40% vegetables and fruit, 33% pasta and bread, 17% of
dairy products (including eggs) and 9% of meat and fish residues, while in Asia, in
and fruits, 34% of rice and noodle, and only a small fraction (around 10%) due to fish,
attention and technical development from the research community in order to promote a
high potential for energy recovery (Capson Tojo et al., 2016; Kuruti et al., 2017;
Zamanzadeh et al., 2016; Zhang et al., 2014) producing carrier material for biofertilizers
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(Kuruti et al., 2017; Shen et al., 2013;). In 2012, 90% of the FW treated in Europe was
processed biologically with both AD and composting according to the Eurostat waste
treatment statistics. The use of AD as a treatment for FWs and other organic wastes has
increased in Europe with a current reported capacity of almost 9 million tons per year in
2015 due to 290 full-scale plants (De Baere and Mattheeuws, 2014) producing methane.
thermophilic digesters operate between 50°C and 55°C. Mesophilic digestion has
always been predominant, because of the small energy needs, and greater stability.
digestion of food waste (Montecchio et al., 2016). In recent years, different novel
reactor designs, such as for example two stage or multiple-stage reactors have been
investigated and developed to reach stable conditions under high organic loading rates
(OLRs) of food waste or OFMSW (Dong et al., 2010). However, the AD of organic
waste generally relies on single-stage systems, which account for more than 95% of
Investigating AD processes for FW conversion has become, for all these reasons, an
exciting research field. For this review, the distribution of the 410 peer-reviewed articles
extracted from literature (Scopus database) in the last 5 years (2012-2017) containing
the fixed term “food waste” in the title combined with biogas (56), or anaerobic
(42) was analyzed also on the basis of affiliation’s country of the authors.
China is unconditionally the most productive country with the largest number of
publications in this research field (more than 40% of the papers) followed by South
Korea (12%), USA (10%) and Japan (5%). In Europe, Italy and Spain researchers are
This review focuses on the anaerobic conversion of FW for energy recovery, in terms of
hydrogen and methane production, reporting the most important results, performances
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and developments taken mainly during the last decade as regards different reactor
configurations (one or multi-stage, dry or wet) and effects of inhibition compounds and
investigated in different regions in the world. Food waste consisting of rice, pasta and
and vegetables is abundant in carbohydrates while food waste consisting of meat, fish
and eggs contains high quantity of proteins and lipids. However, FW presents general
features that can be extrapolated worldwide, with a moisture content of 74-90%, high
volatile solids fraction around 85±5 %, and a mean acidic pH of 5.1±0.7 (Fisgativa et
proved to have varying proportions of nutrients and micronutrients and low presence of
heavy metals, but the variability was very high (Fisgativa et al., 2016). FW typically has
a relatively low C/N ratio, varying between 13.2 and 24.50, lower with respect to the
optimal range of 25-35 assuring efficient digestion conditions (Capson Tojo et al., 2016,
Chen et al., 2008; Zhang et al., 2007). In fact, an excessively high C/N ratio causes the
increase in acid formation inhibiting methane production, while at low C/N ratio
methanogens. For biodegradable substrates, the optimum C/N ratio is in the range 20-
25. However, for materials that are resistant to microbial degradation, the C/N ratio can
be also as high as 40. Due to its fundamental characteristics such as wide availability,
high biodegradable organic fraction and in particular high carbohydrate content, FW has
been considered an attractive economical source for energy production, and substrate
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Zhang et al., 2013a). Organic feedstocks undergo different degradation steps during the
AD process (Fisgativa et al., 2016; Patinvoh et al., 2017). Step one is hydrolysis, where
bacteria producing simple sugars, amino acids, and fatty acids. This step has been
reported as being the rate limiting step for complex, hard biodegradable, organic
substrates (Ariunbataar et al., 2014a, Carlsson et al., 2012; Gianico et al., 2013; Izumi et
al., 2010; Zhang et al., 2014), and can be accelerated by pre-treating the substrate before
digestion (see paragraph 5.2). Step two is acidogenesis, where monomers from the
hydrolysis are fermented into short chain organic acids (acetic, propionic, butyric and
others), alcohols, together with hydrogen and carbon dioxide. The products formed vary
with the types of bacteria as well as environmental conditions Hydrogen, as the most
fastest step in the AD process, so if the feedstock does not have buffering capacity and
the organic loading rate is too high, the accumulation of volatile fatty acids can result in
a pH drop, which would inhibit the methanogens that produce methane in the final step
(Nagao et al., 2012; Zhang et al., 2014). Step three is the acetogenesis, here the
this step, the acetogenic bacteria can only survive at a very low hydrogen concentration,
so excessive production of hydrogen from the acidogenesis step can inhibit these
bacteria. The last step is the methanogenesis, where methane production takes place
under strict anaerobic conditions, by utilizing the intermediate products (as H2 and
acetate) from the preceding stages. Because of these complex succession of biological
steps and of the close connection of the degradation phases, AD of organics is based on
a delicate balance that may affect the instability of the digesters treating food waste, and
thus the amount of methane produced. Acidification through reactor overload is one of
the most common reasons for process deterioration in anaerobic digesters, and occurs
because of the accumulation of volatile fatty acids fatty acids (VFAs) due to the kinetic
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uncoupling between acid producers and consumers (El-Mashad and Zhang, 2010;
Kawai et al., 2014; Nagao et al. 2012; Ventura et al., 2014). Methanogenesis resulted
complex heterogeneous organic material as food waste. The pH is one of the most
important parameters influencing AD, because all the involved microorganisms are very
sensitive to pH variations, and each process step shows a different pH sensitivity. For
methanogens work optimally in a pH range from 6.5 to 7.2, with a methanogenesis step
is necessary, both in terms of carbon and nitrogen ratio, and of micronutrients as Ca, K,
Mg, Na, P and Fe, indispensable for microorganisms. The feedstock total solids content
(as consequently also the volatile solids) affect the AD process of food waste. So far,
three main types of AD technologies have been developed according to the total solids
(TS) content of feedstocks: conventional wet (< 10% TS), semi-dry (10–20% TS) and
technology, facilitates the dry substrate manipulation with batch and semi-continuous
process, but higher structure cost may be present. With specific reference to the full-
scale industrial application, during the last 5 years dry digestion accounts for about 70
Baeere et al., 2014). The predominance of dry digesters was due to the reduced volume
Extensive effort has been devoted to the production of biomethane from FW through
anaerobic processes, but its economic viability is largely dependent on the efficiency of
1
FW type, pre-treatment and scale (Ma et al., 2017). Scale effect of anaerobic digestion
tests in batch and semi-continuous mode for the technical and economic feasibility of a
full-scale digester treating FW is, in our opinion, very important. Therefore, the first
part of this chapter is dedicated to batch systems and the second one is dedicated to
complex heterogeneous feedstocks as FW, where the organic load (in particular the
readily biodegradable one) affects significantly the performances of the process. In fact,
in batch systems, a reactor is loaded with feed and run to completion until methane
production stops. Batch reactors benefit from technical simplicity, low operating costs,
and, last but not least, short digestion times (in 25-40 days, the test is completed). On
the contrary, in continuous systems, reactors are continuously fed with the feedstock,
allowing a steady-state to be reached in the reactor with a constant methane yield, after
1-2 HRTs (hydraulic residence time). Although continuous reactors have higher
operating costs due to storage and requirements, these reactors are able to maintain and
adapt microorganisms within the system, thereby avoiding lag times associated with
microorganism growth in batch reactors, but methane yields depend strictly on the
organic load (OLR) and HRT applied. In fact, food waste feedstock, generally rich of
of VFAs, overwhelming the methanogenesis and eventually leading to the failure of the
process due to VFA accumulation and decrease in the pH. Alternatively, nitrogen is
released during the digestion process and, depending on pH, OLR and temperature, this
may lead to high concentrations of free ammonia (FAN) in the digester. Inhibition due
to high nitrogen content of the substrate has been reported (Chen et al., 2008). The
yields fluctuation depending on the specific FW processed (Tables 1 and 2). In case of
AD instability remedial measures were introduced, such as alkalinity addition (Liu et al.
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2013; Ventura et al. 2014), feed interruption, mixing, or trace elements addition
Methane production varies with many factors such as inoculum, volatile solids,
ammonia, VFA, pH and temperature. A method to source and determine the feasibility
Potential (BMP) test. Such a test monitors the gas production following the incubation
conditions. Because the BMP of the organic material is very important in the design,
determination have been proposed (Holliger et al., 2016). Under mesophilic conditions
biomethane potential is variable between 200 and 570 mL CH4 g-1VSadded (Ariunbaatar
et al., 2014; Izumi et al., 2010; Kawai et al., 2014; Liu et al., 2012; Zhang et al., 2007;
Some papers reported relatively low methane yields ranging from 100 to 250 mL CH4 g-
1
VSadded (Capson Tojo et al., 2016; Nathao et al., 2013; Yang et al., 2015;) probably due
to acidification during food waste digestion (Liu et al., 2009). An important factor
affecting the performances of batch AD is the substrate to inoculum (S/I) ratio (or the
inverse factor, namely inoculum to substrate ratio, ISR) used. The major task in a one-
stage batch reactor is to prevent VFAs accumulation inside the inoculum particles
during start-up (Kawai et al., 2014). In single-stage batch tests, it is common practice to
load inoculum and substrate based on VS ratios (Pagliaccia et al., 2016). Although
theoretically, the S/I ratio has an effect only on the kinetics, the influence of S/I on
biomethane production has been commonly investigated during batch tests, and specific
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studies on the effect of this ratio for different FW have been carried out (Liu et al.,
2009; Lü et al., 2012; Pagliaccia et al, 2016). It is worth to note that methane yields,
obtained from single-stage mesophilic batch tests operated at S/I ≤ 0.5, range all
between 417 and 529 L CH4 kg-1VSfed (Ariunbataar et al., 2015; Browne and Murphy,
2013; Facchin et al., 2013; Kawai et al., 2014; Völklein et al., 2016) evidencing stability
of the process (Table 1). Most studies suggested that using S/I ratio below 1.0 was
enough to prevent acidification (Elbeshbishy et al., 2012; Kawai et al., 2014). Methane
yields lower than 100 L CH4 kg-1VSfed are generally related to the extremely high S/I
ratios applied, and short duration time (Nathao et al., 2013). Liu et al. (2009) performed
thermophilic BMP assays on food waste at S/I ratios from 1.6 to 5.0 and reported that
anaerobic biodegradability decreased with the rise of S/I ratios. However, when the
inoculum was completely mixed with the waste, methanogenesis was not initiated even
at S/I of 0.9 (Lü et al., 2012). In contrast, when the inoculum was initially separated
from the waste in a double-reactor system (and connected by the controlled exchange of
fermented waste), the waste could be effectively transformed to methane even at S/I
18.9 (Lü et al., 2012). The instability of the process due to acidification results also
transformed to VFAs in the initial phase of AD (Kawai et al., 2014). In fact, the
methane yields from the same FW, without LOF rich supernatant, were relatively stable
in all S/I conditions, although the maximum methane yield was lower compared to the
raw FW (Kawai et al., 2014). Moreover, excessive reduction of the particle size of the
al., 2010). The impact of the solubilized matter, in particular sugars, on VFA
account when feedstock pre-treatments are selected and optimized (see paragraph 5.2),
otherwise the strategy can be detrimental rather than beneficial. Zero-valent iron
degree of imbalance and higher risk for ammonia inhibition than mesophilic process
temperatures, and in fact only few studies have focused on the thermophilic AD of FW
(Liu et al., 2009; Yang et al., 2015; Zhang et al., 2007). Controversial results regard the
impact of inoculum acclimation on methane conversion rate during BMP tests. While
Browne and Murphy (2013) highlighted that for accurate BMP assessment the inoculum
laboratories evidenced that it was not necessary that the inoculum was specifically
adapted to the substrates to be tested (Holliger et al., 2016). Effect of the inoculum
source was observed also by Facchin et al. (2013) where using the inoculum originated
from a reactor co-digesting FW and sludge generated more methane than using an
inoculum originated from an anaerobic reactor treating only FW. The primary parameter
for the selection of inoculum is the soluble COD concentration, which reflects the
“health status” of the provenance digester. In the study of Elbeshbishy et al., 2012, in
fact, the FW digester inoculum had five times higher soluble COD concentration than
the municipal sludge digester, suggesting important differences between the ratio of
between the two inocula. The growth of methanogens is dependent on many ions such
as sodium, nickel, cobalt, iron, zinc, magnesium, calcium and potassium cations and
elements (TEs) have been studied for the AD of FW. Facchin et al. (2013) achieved a
Mo, Ni, Se, and W) cocktail, and stressed the importance of Se and Mo for the
biomethane production.
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3.2 Continuous AD tests for methane production
microbial community and inoculum quality used for the start-up of an anaerobic reactor
are also critical factors for successful biogas production (Elbeshbishy et al., 2012;
necessary. Stable digestion can be assumed when the measured parameters, such as the
within 10% of their average values, for a minimum period of one HRT. For all these
reasons, the semi-continuous tests need long time duration, but sometimes literature
data originate from too rushed digestion tests with duration shorter than the applied
Table 2 summarizes the best performances in terms of methane yields and VS removal
(if available) for single and dual stage digestion systems reported in literature. Stable
AD of FW was usually attained for HRT ranging between 16-40 days and OLRs lower
than 4.5 gVS L-1d-1 (table 2). High buffer capacity, due to released total ammoniacal
nitrogen (TAN) allows AD to operate at higher organic loading rates (OLRs), thus
et al., 2015). Nevertheless, Chen et al. (2008) reported that TAN concentrations ranging
from 1700 mg L-1 to 14000 mg L-1 all decreased methane yield by more than 50%,
studies. Serna-Maza et al. (2014) studied on the efficient performance and stability of
35L anaerobic digesters fed on food waste coupled to side-stream ammonia stripping
columns, but high stripping temperature (70°C) and a pH of 10 are needed. Selenium,
which is present only in low concentrations in FW, has been shown to be essential in
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recovering a digester suffering from a propionic acid accumulation due to elevated
ammonia concentrations, while at higher organic loading rates additional cobalt is also
Trace metals (Fe, Co, Ni) requirement per COD removed was obtained experimentally
required Fe to Ni and Co were about two times higher in thermophilic system than those
A novel approach was the application of a dual solid–liquid (ADSL) system, involving
the use of two digesters for FSW (food solid waste) and FLW (food liquid waste
without waste oil) digestion, where optimum OLRs for FSW, FLW and raw FW were 9,
4 and 7 gVS L-1d-1, and the corresponding methane yields 540, 390 and 405 mL g-1VS,
respectively (Zhang et al., 2013a). Ghanimeh et al. (2012) examined the effect of
mixing and non-mixing strategies on the performance of thermophilic digesters, and the
digester with mixing showed better stability minimizing VFA production. Considering
increasing the temperature, the proportion of the most toxic form of ammonia, namely
FAN, also increased, with detrimental effect on thermophilic process stability and
methane yields (Chen et al. 2008; Yirong et al., 2015; Zamanzadeh et al., 2016). The
acquisition of the conductivity and the online alkalinity measure are robust indirect
parameters to predict the content and the variation of ammonia concentration to avoid
inhibitory issues (Micolucci et al., 2014). In the recent years, considerable attention has
been paid towards the development of high rate bioreactors with maximum treatment
efficiency, basically designed to minimize HRT and increase rate of biogas production
hence marking the fact that the reactor design has a strong effect on digester
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conditions using an horizontal-type cylindrical reactor, and stable dry AD was achieved
by HRT control (more than 40d) without the addition of alkali agents, attaining average
CH4 production rate of 2.51 ± 0.17 m3 m-3 d-1 (Cho et al., 2013). The rapid acidification
phenomena observed at loading 4.9 kg VS m-3 d-1 to the high rate biomethanation
technology called ‘‘Anaerobic gas lift reactor” (AGR) was worthy from the perspective
of giving readily available soluble compounds to the methanogens in the digester and
decreasing HRT for biodegradable organic matter removal (Kuruti et al., 2017).
However, this phenomenon could cause instability in the digester due to pH drop unless
buffering capacity of the digester was enhanced externally. To overcome this problem,
milk of lime was added in the feed tank to maintain the pH of the feed slurry around
the purpose of optimizing reactor conditions for the distinctly different microbes that
carry out these functions. The first stage (acid fermentation) is maintained at low pH
and short hydraulic residence times (HRT; 2–3 days) resulting in a washout of acid-
Two stage AD systems may be less susceptible to system overloading with increased
specific activity of methanogens resulting in a higher methane yield (Shen et al., 2013;
Wang and Zhao, 2009;). Optimizing two-stage conditions may result in the production
of hydrogen from the primary reactor and methane from the second reactor, making it a
very attractive bio-energy producing system. Numerous studies have been conducted on
the optimization of such systems with reactors both at mesophilic and/or thermophilic
temperatures, optimizing HRT and OLR in particular of the first reactor (see Table 3).
Best operative conditions and results as regards on hydrogen production are widely
discussed in the next paragraph. In terms of methane yields, the two-stage AD process
may provide unique benefits when treating high strength waste such as FW at high load.
In fact, by digesting FW with fruit and vegetable waste at low OLRs (<2.0 g VS L-1 d-1),
1
single-phase AD resulted better than two-phase AD in terms of CH4 production (up to
+4%), while at higher level of OLR two-phase digestion achieved higher CH4
production (Shen et al., 2013). Single and two-phase operations were compared also at
higher scale using a digester system consisting of 5 m3 reactors treating FW and higher
single-stage operation (380 vs 446 L CH4 kg VS-1 L-1), but it must be pointed out that
the applied VS loading rate for the single stage was significantly higher with respect to
the two-stage (Grimberg et al., 2015). Yan et al. (2016) optimized acidogenic off-gas
utilization in a methanogenic UASB reactor for utilization of H2 and CO2 via direct
introduction of external hydrogen into the anaerobic digester and the consequent
promotion of the
upgrading.
High rate digester, based on two-stage technology, was designed for the treatment of
average biogas production of 0.16 m3 kg-1 VS d-1 with 50-60% of methane (Dahiya and
systems digesting FW, obtaining high methane yields and avoiding inhibition by
(Chinellato et al., 2013; Lee et al., 2010; Micolucci et al., 2014), while operating two-
stage thermophilic reactors without recirculation generated low methane yields despite
the low TS content of the feed (Chu et al., 2012). Moreover, some studies have
the stages. Ventura et al. (2014) reported the highest methane yields with a mesophilic
first stage and a thermophilic second stage, but the process was found to be less stable at
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4. Anaerobic conversion of food waste into hydrogen
the development of sustainable energy systems, having the highest energy per unit
weight (143 kJ kg-1) of any known gaseous fuel. Dark fermentation (DF) of low value
waste biomass is the most feasible biological technology for hydrogen production due
to its low energy requirements and high production rates meeting the circular economy
pathways can occur during DF of FW, depending on the adopted operating conditions,
evolution is related to acetate and butyrate pathways, which involve the production of,
respectively, 4 and 2 mol of molecular H2 per mol of glucose degraded (i.e. 544 and 272
pathways leading to the formation of other products (propionate, ethanol and lactic acid)
lower the H2 production (de Gioannis et al., 2013). As a result, the actual hydrogen yield
is always lower than the theoretical one. Operational parameters including substrate
type, inoculum type and origin, pre-treatment type, temperature, pH, reactor
configuration, OLR and HRT are the main factors affecting the H2 conversion rate (de
through DF of FW has been published; most of these experiments have been conducted
at lab or pilot scale (Jayalakshmi et al., 2009; Wang and Zhao, 2009), while no data on
operating conditions have been applied, so that the reported results are difficult to
Table 3. Best operating conditions and H2 yields from food waste fermentation
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An attempt to discuss, critically, the relative importance of each parameter, as well their
parameter, the results reported in Table 3 refer to the best H2 yield or optimal system
The seed microorganisms used as inoculum represent a key factor for H2 fermentation.
In fact, most researchers use mixed microbial cultures, such as sludge, soil or compost,
because of low costs, easiness in control and high versatility (de Gioannis et al., 2013).
However, by using mixed microflora, the coexistence of H2- producing and consuming
inoculum is generally pre-treated. This process step relies on the better chance of
due to their ability to form spores. The reported pre-treatments are heat-shock treatment
(HST), aeration, addition of chemical compounds, acid or alkali treatment, freezing and
thawing. The most common approach is HST, which is generally carried out at
temperature of 80-100 °C for 10-30 min (Chu et al., 2012; Elsamadony et al., 2015;
Gadhe et al., 2014; Han et al., 2015; Jayalakshimi et al., 2009; Kobayashi et al., 2012;
Lee et al., 2010; Nathao et al., 2013; Rafieenia et al., 2017; Voelklein et al., 2016;).
Only few studies have been conducted without inoculum pre-treatment with the aim of
reducing costs (Algapani et al., 2016; Shen et al., 2013; Tawfik and El-Qelish, 2012;
2011a; Jang et al., 2015; Kim et al., 2011; Wang and Zhao, 2009), by pre-treating the
lactic acid bacteria (LAB). Based on the results of their previous tests, Kim et al.,
(2011), applied HST treatment to FW without inoculum addition, as they found that
1
increasing the H2/butyrate production. The effect of alkali-shock was investigated by
Jang et al. (2015) and maximal H2 yield in batch was obtained by pre-treating the FW at
thermophilic conditions (Table 3). Many authors agree that thermophilic conditions are
Clostridia, to inhibit the activity of H2 consumers and to suppress the growth of LABs,
thus assuring higher H2 yields. Process temperature shows a significant effect on the
the fermentation medium: lactate was found to be predominant at 35°C, while butyrate
was the main product at 50°C. pH is considered one of the most crucial operational
pathway, and dominant microbial population. Optimal pH values have been reported in
the range of 5.0–6.5 when the predominant metabolic pathways are those associate with
acetate and butyrate production. On the contrary, neutral or higher pH seemed to favour
ethanol and propionate production. Moreover, if pH drops at very low values (≤ 4.5) a
metabolic shift could occur which leads to lactic acid accumulation (zero-H2 pathway)
system is usually maintained at the optimal operating value by buffer or alkali solutions
addition (Han et al. 2015; Kim et al, 2011; Jang et al, 2015), particularly in continuous
H2-producing reactors. Moreover, the influence of initial pH was correlated to lag phase
duration, synthesis of enzymes and spore germination (in heat pre-treated inoculum)
and the maximal H2 production was observed for initial pH around 8 (de Gioannis et al.,
systems, internal recirculation of the effluent from the methanogenic phase has been
proposed as an efficient strategy to control pH in the optimal range for the hydrogen
1
producing bacteria, thus improving the efficiency and economics of the DF process
(Chinellato et al. 2013; Yeshanew et al., 2016). Nevertheless, controversial results were
sludge an inhibitive effect on H2 production was observed, probably due to the high
Moreover, in long-term operation, special attention must be paid also to the increase of
production studies have been performed by means of small laboratory vessels or stirred
mode. The organic load applied to the reactor greatly affects the system performances,
active biomass composition. Concerning batch systems, also in the case of hydrogen
production, some studies proved that S/I ratio influences the efficiency of the process,
and, contrary to what was observed for methane yields, efficient H2 production are
strictly related to high S/I ratios (Nathao et al., 2013; Pan et al., 2008;). Under
while under mesophilic conditions the highest yield of 39 mL H2 g-1VS was attained at
S/I of 6 (Pan et al., 2008). For semi-continuous and continuous operations, the HRT is
efficiency, but also the type of active microbial population and the metabolic pathways
production due to methanogens wash-out from the reactor, while long HRTs favour the
growth of methanogenic activity and non H2-producing acidogens inside the active
biomass. Therefore, both OLR and HRT need optimization as controlling parameters to
reported in Table 3, most researchers, with very few exceptions, have set HRT in the
range 1-4 days (de Gioannis et al., 2013; Redondas et al., 2012), operating at high OLRs
1
from 8 to 40 kgVS m-3d-1. Nevertheless, hydrogen yield up to 38 L H2 kg-1VSfed was
at OLR 66 g VS L-1d-1 with a mixture of food waste and OFMSW. The stepwise
increase of the OLR from 15.10 to 37.75 kgVSfed m-3d-1 may cause a decrease of H2
integrated two-stage process (Wang and Zhao, 2009). Also Voelklein et al., (2016)
noted a close correlation between increasing OLRs of fermentation reactor (6-15 kgVS
L-1d-1), with fixed SRT of 4 days, and high quantities of ethanol and lactic acid in the
fermentation broth. The continuous stirred tank reactors (CSTR) is the most commonly
used reactor type, as the biomass is suspended and well mixed in the fermentation
reactors have been exploited, too. Continuous mixed immobilized sludge reactor
(CMISR) and anaerobic baffled reactor (ABR) were used, respectively, by Han et al.,
(2015) and Tawfik and El –Qelish, (2012) in order to enhance biomass retention in the
allow operating the reactors at higher OLRs compared to CSTRs, maintaining a stable
to one stage H2 fermentation, higher gas yields are generally reported in batch
experiments rather than with semi-continuous or continuous operations (Table 3). This
is probably related to the short period in batch fermentation, which permits to easier re-
productions and yields. On the contrary, for long term operations, the continuous
feeding of a low buffering capacity substrate as FW could likely lead to system failure
due to pH drop, low nitrogen input, and biomass metabolic shifting. Unfortunately, even
content remains in the effluent from the H2 fermentation, promoting research activity
1
and technological development towards the just mentioned two-phase AD systems to
improve the overall FW conversion yields recovering both hydrogen, from first, and
methane, from second reactor. In two-stage systems, the first reactor is generally
operated at lower OLRs with respect to those applied for one stage reactors (Table 3),
60 and 150 mL H2 g-1VS, and are significantly higher with respect to those obtained in
mesophilic ones.
characteristics and composition but also the final aim of the study. In fact, feedstock
performances when hydrolysis is the rate limiting step, while, in the case of
biodegradable FW, the long-term digestion leads often to inhibition phenomena due to
stabilize the entire process (Wang et al., 2014). In the subsequent paragraphs both
nutrients (El-Mashad and Zhang, 2010; Gou et al., 2014; Liu et al., 2013; Mata Alvarez
et al., 2014; Nghiem et al., 2017). In the literature of the last years, various organic
waste streams have been investigated to co-digest FW for biogas production, and the
most frequent are animal manures, sewage sludge, green waste and agro-waste (Mata-
Alvarez et al., 2014). The mixture ratios are selected in order to favor positive
1
interactions as for instance the right nutrients and moisture balance, to avoid inhibition
and to optimize methane production (Zhang et al., 2012). However, the wrong
combination of co-substrates can lead to negative results. The most important literature
summarized in Table 4.
low C/N ratio and for its wide variety of macro- and micronutrients needed by the
anaerobic consortium of microorganisms. Zhang et al. (2012) confirmed that the co-
digestion of FW with cattle slurry, in 20:80 ratio, permitted to reach greater stability
operating at OLR of 2 kg VS m-3 day-1. Operating at the same OLR, Agyeman and Tao
(2014) investigated the effects of FW particle size on co-digestion with dairy manure
(50:50), finding that specific methane yield increased up to 630 L CH4 kg-1VSfed feeding
good methane yields and stability by co-digesting FW and cow manure (Rajagopal et
al., 2017). It is worth to note that in most published papers, the mixtures of FW and
animal waste matter are typically composed by low percentages of FW (ideal substrate
for H2 production due to the high content of sugars), consequently no data are available
in the literature as regards hydrogen generation during co-digestion. Another typical co-
substrate of FW is sewage sludge, characterized by low C/N ratio and low organic
content that guarantee the C/N balance improving microbial activity and lowering
intermediate accumulation, as ammonia (Dai et al., 2013; Liu et al., 2013) ). In fact,
during co-digestion batch tests no process failure was reported and methane production
increased significantly (Naran et al., 2016; Zhang al., 2016). In semi-continuous co-
digestion of FW and WAS (33:67 ratio) the contemporary increase of HRT from 160d
methane yield and VS reduction rate (Gou et al., 2014). Operating a mesophilic digester
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at shorter HRT (20d) and high OLRs (up to 7.6 g VS L-1d-1), co-digestion with
dewatered sludge assured stability and higher methane yields, with respect to those
observed with WAS (Dai et al., 2013). As just highlighted for animal waste, also for
sewage sludge hydrogen production from co-fermentation with FW is still limited (Liu
et al., 2013). Hydrogen yields ranging from 10 to 104 L H2 kg-1VSfed were obtained in
batch mode with high S/I (up to 4) treating different mixtures of FW, primary sludge
and WAS. As expected, the higher the FW content in the mixture, the higher was the H2
yield (Zhu et al., 2008). Liu et al. (2013) obtained up to 106 L H2 kg-1VSfed and 354 L
CH4 kg-1VSfed with the 85% of FW in a two-stage co-digestion batch system with WAS.
synergies for the water industry and authorities responsible for FW management (Zhang
necessary to face these challenges and to promote co-digestion as a key technology for a
circular economy (Nghiem et al., 2017). Besides sewage sludge or animal manures,
agro-food waste and green waste are other possible co-substrates with FW, mainly
because of the very low cost associated with their collection (Chen et al., 2014).
challenges, because of the poor nutrient content, long retention times and potential high
levels of inhibitory compounds (Gianico et al., 2013). At the same time, the high
content of recalcitrant lignin in green/agro waste might reduce the biodegradable rate of
FW (Drennan and Di Stefano, 2014), thus reducing the risk of VFAs accumulation
(Chen et al., 2014; Rizwan Haider et al., 2015). The relatively low biodegradability of
increase the C/N ratio (Drennan and Di Stefano, 2014). Co-digestion of FW with a
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substrate with high content of bioavailable carbon is therefore recommended to allow
rice husk in a pilot scale plug-flow reactor and, biogas production, reactor stability and
Owamah and Izinyon (2015) obtained increasing methane yields (up to 482 L CH4 kg-
1
VS) by increasing the OLR, up to 4.5 gVS L-1d-1, in a co-digestion of FW with maize
husk, probably due to the appropriate high FW fraction (i.e. 75%). An increase in
straw was reported by Yong et al. (2015). As regards batch co-digestion, also in this
case an inverse correlation between CH4 yield and load (expressed as S/I) was observed,
during mesophilic and thermophilic co-digestion of FW with green waste or rice husk
(Liu et al., 2009; Rizwan Haider et al., 2015). Interesting prototypes as single-stage
(2,500 L) and two-stage (1,000 L + 2,500 L) anaerobic digesters treating FW and rain
tree leaf have been developed and operated at high OLRs, resulting in high VS removal
efficiencies, but poor CH4 yields (153 L CH4 kg-1VSfed and 283 L CH4 kg-1VSfed for
single- and two-stage) (Ratanatamskul and Manpetch, 2016). The feasibility of the co-
digestion process of FW with a further wide range of other co-substrates has been
widely investigated. Zhang et al. (2015b) studied the co-digestion with fresh leachate
rich in trace elements and alkalinity promoting therefore methane production assuring
buffering ability of AD system. Paudel et al. (2017) carried out a two-stage co-digestion
of FW with brown wastewater, obtaining up to 99.8 L H2 kg-1VSfed in the first stage and
up to 728 L CH4 kg-1VSfed in the second stage. The use of de-oiled gras trap waste as co-
Every pre-treatment, in fact, acts with a different mechanism, with several variables
playing a role and it is therefore difficult to compare them and to assess the “ideal” pre-
1
treatment type because of the lack of common and standardised protocols (Carlsson et
al., 2012). In this section, the pre-treatments applied to food waste have been revised
and evaluated taking into consideration both solubilisation and H2/CH4/biogas yields.
Table 5 reports the best combination of pre-treatment parameters, leading to the best
performance, i.e. the one that had the highest gain in H2/CH4/biogas yield if compared
soluble COD measure) is not directly related to the subsequent gain in CH4 or H2 yield,
but sometimes the correlation is even negative. This leads to an urgent need in
understanding more deeply the inner mechanisms of the various pre-treatments on the
proteins, lipids and lignocellulosic fractions present in organic waste are associated to
pre-treatment. Moreover, most FW pre-treatments have been still studied in lab scale
batch reactors, while semi-continuous trials are still very limited (Table 5). In this
milling, and to screen FW (screw press, disc screens, magnets, etc.) were not considered
Thermal pre-treatments have been extensively investigated and are already implemented
in full-scale for what concerns sewage sludge and lignocellulosic biomasses. Its
mechanism of action significantly alters both physical and chemical properties, resulting
degree of solubilisation, but this is not always connected to a final energy yield gain. At
160°C lignin solubilisation starts, but at the same time lignin solubilisation is
responsible for the formation of inhibitory phenolic compounds. For temperature higher
than 170°C there might be also some condensation reactions (e.g. Maillard reactions)
1
which turns out to be hardly biodegradable or even refractory (Ariunbataar et al., 2014).
So, for all these reasons, increased yields have been mostly observed in the lower
temperature range, and main results show a decreased yield related to high T pre-
treatment (Table 5), while there is an increasing trend of CH4 yield at T<120°C. Tampio
et al. (2014) and Liu et al. (2012), reported a 7.9 ÷ 11.7 % decrease in methane yields
after thermal pre-treatment at T > 160°C, even though a high solubilisation degree.
upgrade in hydrogen production by pure culture was obtained (Hu et al., 2014) Most of
the pure cultures tested (3 out of 4) were efficient in utilizing FW to produce H2 and
gave a substantial yield gain even without pH control (Hu et al., 2014). Similar results
were reported for a single stage AD of pre-treated cafeteria FW, where sugars
yield because of the lack of bioavailable substance just transformed (Pagliaccia et al.,
conventional heating because of lower energy requirements (no heat loss through
hydrogen bonds breakage. Nonetheless, results are not that satisfactory: despite an
increase of organics solubilisation with T, biogas gain at 115°C was only 8%, and AD
process collapsed for the 175°C pre-treated samples (Shahriari et al., 2012),
semi-continuous tests, the results were not satisfactory (Shahriari et al., 2013).
characteristics and they exclude the risk of inhibitory compounds formation, but they all
forces. Gadhe et al.(2014) and Elbeshbishy et al. (2011a) applied ultrasounds for H2
1
food waste at high specific energy. Solubilisation was directly proportional to sonication
time and energy, but the degree of solubilisation was generally lower compared to that
+50% gain by sonicating the substrate at 7300kJ kg-1TSS (Naran et al., 2016). Anyway,
specific methane yield of control AD with untreated FW was very low, namely 137 mL
CH4 g-1VSSrem versus a typical average value of 400±30 mL CH4 g-1 VSrem. This might
be due to the high value of the S/I chosen (60 on VSS based), which might have led to
inhibition of the process. Zou et al. (2016) tried a first attempt of HVPD (high voltage
plate reactor, which creates a rapidly pulsing (several kHz), high-voltage electric field to
disrupt and break up the cellular membrane, complex organic solids, and
control, and from the point of energy usage efficiency, output methane production was
calculated to be equal to 5.7 times than energy consumption, which makes it more
Biological pre-treatments include both enzymatic and aerobic methods (to enhance
the digester. As pre-treatment there is the inherent risk that released sugars are rapidly
might be required but this option is generally too expensive to be pursued in full-scale
implementation. In full-scale scenario, adding the enzymes directly in the digester is the
most usual configuration (Carrere et al., 2016). Generally, even though enzymatic pre-
treatments require much less energy input than mechanical and thermal ones without
1
efficiency remain major issues. Moreover the relatively long contact time needed (24h
at least) might not be a feasible option for full-scale plants, despite the high methane
enhancement obtained in batch tests (Kiran et al., 2015; Yin et al., 2016). Aeration prior
accumulation of VFAs, thus improving the start-up stability of AD. Rafieenia et al.
AD highlighting that average hydrogen production decreased, probably due to the low
SRT (3 d) in the first reactor and parallel consumption of the readily biodegradable
carbon for microbial cell growth during substrate aeration. However, during the
subsequent stage, CH4 production was higher for pre-aerated protein- and carbohydrate-
rich samples than in non-pre-aerated ones; conversely, pre-aeration of the lipid rich-
untreated sample.
Strong acids, alkalis or oxidants are commonly used reagents to solubilise biopolymers
conversion. Solubilisation levels achieved with chemical pre-treatments are usually very
high, much higher with respect to those obtained with other pre-treatments, but the risk
Because of the high solubilisation capacity, chemical pre-treatment is not suitable for
easily biodegradable substrates such as FW: high rate carbohydrates degradation and
1
lower the severity of each pre-treatment reducing the intrinsic disadvantages as
enzyme, energy costs. Combination is also applied in the case a single pre-treatment is
not sufficient to obtain the desired result due to its specific mechanism of action.
Elbeshbishy et al. (2011a) tried to couple ultrasonic with acid, alkali and heat shock pre-
treatment for H2 production without using extra seed (FW was inoculum and substrate
at the same time). The only significant increase compared to the single pre-treated
sample was due to acid addition, resulting in +181% higher hydrogen yield than the
control. Even though results are promising in this case, an economic analysis is needed
Conclusions
This review explored recent advances in the research field of FW conversion into
energy in the framework of the circular economy. It resulted that FW is a complex and
can vary significantly during the scaling up of the process, from batch BMP tests to
solubilization, since hydrolysis is not necessarily the limiting step, and the risks related
processes, as bubble columns for selective desorption of CO2 need more applicative
research.
Acknowledgements
This work was supported by the PRIN 2012 project titled “Advanced Processes to
1
the Italian Minister of University and Scientific Research (MIUR). Authors wish to
thank dr. Giuseppe Mininni and Prof. Fausto Gironi for their valuable support.
1
References
1. Agyeman, F.O., Tao, W., 2014. Anaerobic co-digestion of food waste and dairy manure:
Effects of food waste particle size and organic loading rate. J. Environ. Manag. 133, 268-
274.
2. Algapani, D.E., Qiao, W., Su, M., di Pumpo, F., Wandera, S.M., Adani, F., Dong, R., 2016.
Bio-hydrolysis and bio-hydrogen production from food waste by thermophilic and
hyperthermophilic anaerobic process. Bioresour. Technol. 216, 768-777.
3. Angeriz-Campoy, R., Álvarez-Gallego, C.J., Romero-García, L.I., 2015. Thermophilic
anaerobic co-digestion of organic fraction of municipal solid waste (OFMSW) with food
waste (FW): enhancement of bio-hydrogen production. Bioresour. Technol. 194, 291–296.
4. Ariunbaatar, J., Panico, A., Frunzo, L., Esposito, G., Lens, P.N.L., Pirozzi, F., 2014.
Enhanced anaerobic digestion of food waste by thermal and ozonation pretreatment
methods. J. Environ. Manage. 146, 142–149.
5. Ariunbaatar, J., Di Perta, E.S., Panico, A., Frunzo, L., Esposito, G., Lens, P.N.L., Pirozzi,
F., 2015. Effect of ammoniacal nitrogen on one-stage and two-stage anaerobic digestion of
food waste. Waste Manag. 38, 388–398.
6. Browne, J.D., Murphy, J.D., 2013. Assessment of the resource associated with biomethane
from food waste. Appl. Energy 104, 170–177.
7. Capson-Tojo, G., Rouez, M., Crest, M., Steyer, J.-P., Delgenès, J.-P., and Escudié, R.,
2016. Food waste valorization via anaerobic processes: a review. Rev. Environ. Science
and Bio/Technol. 15(3), 499-547.
8. Carlsson, M., Lagerkvist, A., Morgan-Sagastume, F., 2012. The effects of substrate
pretreatment on anaerobic digestion: a review. Waste Manage. 32, 1634–1650.
9. Carrere, H., Antonopoulou, G., Affes, R., Passos, F., Battimelli, A., Lyberatos, G., Ferrer,
I. 2016. Review of feedstock pretreatment strategies for improved anaerobic digestion:
from lab-scale research to full-scale application. Bioresour. Technol. 199, 386–397.
10. Castrillón, L., Marañón, E., Fernández-Nava, Y., Ormaechea, P., Quiroga G., 2013.
Thermophilic co-digestion of cattle manure and food waste supplemented with crude
glycerin in induced bed reactor (IBR). Bioresour. Technol. 136, 73–77.
11. Chen, Y., Cheng, J.J., Creamer, K.S., 2008. Inhibition of anaerobic digestion process: A
review. Bioresour. Technol. 99, 4044-4064.
12. Chen, X., Yan, W., Sheng, K., Sanati, M., 2014. Comparison of high solids to liquid
anaerobic co-digestion of food waste and green waste. Bioresour. Technol. 154, 215–221.
13. Chinellato, G., Cavinato, C., Bolzonella, D., Heaven, S., Banks, C.J., 2013. Biohydrogen
production from food waste in batch and semi-continuous conditions: evaluation of a two-
phase approach with digestate recirculation for pH control. Int. J. Hydrogen Energy 38,
4351–4360.
14. Cho, S.K., Im, W.T., Kim, D.H., Kim, M.H., Shin, H.S., Oh, S.E., 2013. Dry anaerobic
digestion of food waste under mesophilic conditions: Performance and methanogenic
community analysis. Bioresour. Technol. 131, 210-217.
15. Chu, C.F., Xu, K.Q., Li, Y.Y., Inamori, Y., 2012. Hydrogen and methane potential based
on the nature of food waste materials in a two-stage thermophilic fermentation process. Int.
J. Hydrogen Energy 37(14), 10611-10618.
16. Dahiya, S., Joseph, J., 2015. High rate biomethanation technology for solid waste
management and rapid biogas production: An emphasis on reactor design parameters.
Bioresour. Technol. 188, 73-78.
17. Dai, X., Duan, N., Dong, B., Dai, L., 2013. High-solids anaerobic co-digestion of sewage
sludge and food waste in comparison with mono digestions: Stability and performance.
Waste Manag. 33, 308–316.
18. De Baere, L., Mattheeuws, B., 2014. Anaerobic digestion of the organic fraction of
municipal solid waste in Europe -Status, experience and prospects in: Waste Management,
Vol 3 Recycling and Recovery, TK, pp. 517- 526.
19. De Gioannis, G., Muntoni, A., Polettini, A., Pomi, R., 2013. A review of dark fermentation
hydrogen production from biodegradable municipal waste fractions. Waste Manag. 33(6),
1345-1361.
1
20. Dennehy, C., Lawlor, P.G., Croize, T., Jiang, Y., Morrison, L., Gardiner, G.E., Zhan, X.,
2016. Synergism and effect of high initial volatile fatty acid concentrations during food
waste and pig manure anaerobic co-digestion. Waste Manag. 56, 173–180.
21. Dong, L., Zhenhong, Y., Yongming, S., 2010. Semi-dry mesophilic anaerobic digestion of
water sorted organic fraction of municipal solid waste (WS-OFMSW). Bioresour. Technol.
101, 2722–2728.
22. Drennan, M.F., Di Stefano, T.D., 2014. High solids co-digestion of food and landscape
waste and the potential for ammonia toxicity. Waste Manag. 34, 1289–1298.
23. Elbeshbishy, E., Hafez, H., Dhar, B.R., Nakhla, G., 2011a. Single and combined effect of
various pretreatment methods for biohydrogen production from food waste. Int. J.
Hydrogen Energy 36, 11379–11387.
24. Elbeshbishy E., Hafez H., Nakhla, G., 2011b. Ultrasonication for biohydrogen production
from food waste. Int. J. Hydrogen Energy 36, 2896–2903.
25. Elbeshbishy E., Nakhla, G., Hafez., H., 2012. Biochemical methane potential (BMP) of
food waste and primary sludge: influence of inoculum pre-incubation and inoculum source.
Bioresour. Technol. 110, 18–25.
26. El-Mashad, H.M., Zhang, R., 2010. Biogas production from co-digestion of dairy manure
and food waste. Bioresour. Technol. 101, 4021-4028.
27. Elsamadony, M., Tawfik, A., Suzuki, M., 2015. Surfactant-enhanced biohydrogen
production from organic fraction of municipal solid waste (OFMSW) via dry anaerobic
digestion. Appl. Energy 149, 272–282.
28. Facchin,V., Cavinato,C., Fatone,F., Pavan,P., Cecchi,F., and Bolzonella, D., 2013. Effect
of trace element supplementation on the mesophilic anaerobic digestion of food waste in
batch trials: the influence of inoculum origin. Biochem. Eng. J. 70, 71-77.
29. Fisgativa, H., Tremier, A., Dabert, P., 2016. Characterizing the variability of food waste
quality: a need for efficient valorization through anaerobic digestion. Waste Manag. 50,
264-274.
30. Gadhe, A., Sonawane, S.S., Varma, M.N., 2014. Ultrasonic pretreatment for an
enhancement of biohydrogen production from complex food waste. Int. J. Hydrogen
Energy 39, 7721-7729.
31. Ghanimeh, S., El Fadel, M., Saikaly, P., 2012. Mixing effect on thermophilic anaerobic
digestion of source-sorted organic fraction of municipal solid waste. Bioresour. Technol.
117, 63-71.
32. Gianico, A., Braguglia CM, Mescia D, Mininni G. 2013 Ultrasonic and thermal
pretreatments to enhance the anaerobic bioconversion of olive husks. Bioresour. Technol.
147, 623-626.
33. Gou, C., Yang, Z., Huang, J., Wang, H., Xu, H., Wang, L., 2014. Effects of temperature
and organic loading rate on the performance and microbial community of anaerobic co-
digestion of waste activated sludge and food waste. Chemosphere 105, 146–151.
34. Grimberg, S.J., Hilderbrandt, D., Kinnunen, M., Rogers, S., 2015. Anaerobic digestion of
food waste through the operation of a mesophilic two-phase pilot scale digester -
assessment of variable loadings on system performance. Bioresour. Technol. 178, 226–229.
35. Han, W., Liu, D.N., Shi, Y.W., Tang, J.H., Li, Y.F., Ren, N.Q., 2015. Biohydrogen
production from food waste hydrolysate using continuous mixed immobilized sludge
reactors. Bioresour. Technol. 180, 54–58.
36. Holliger, C., Alves, M., Andrade, D., Angelidaki, I., Astals, S., Baier, U., Bougrier, C. et
al., 2016. Towards a standardization of biomethane potential tests. Water Science Technol.
74(11), 2515-2522.
37. Hu, C.C., Giannis, A., Chen, C.-L., Wang, J.-Y., 2014. Evaluation of hydrogen producing
cultures using pretreated food waste, Int. J. Hydrogen Energy, 39, 19337–19342.
38. Izumi, K., Okishio, Y., Nagao, N. et al., 2010. Effects of particle size on anaerobic
digestion of food waste. Int. Biodeterior. Biodegrad. 64, 601–608.
39. Jabeen, M., Zeshan, Yousaf, S., Rizwan Haider, M., Malik, R.N., 2015. High-solids
anaerobic co-digestion of food waste and rice husk at different organic loading rates. Int.
Biodeterior. Biodegrad. 102, 149-153.
40. Jang, S., Kim, D.H., Yun, Y.M., Lee, M.K., Moon, C., Kang, W.S., Kwak, S.S., Kim,
M.S., 2015. Hydrogen fermentation of food waste by alkali shock pretreatment: microbial
community analysis and limitation of continuous operation. Bioresour. Technol. 186, 215–
222.
1
41. Jayalakshmi, S., Joseph, K., Sukumaran, V., 2009. Bio hydrogen generation from kitchen
waste in an inclined plug flow reactor. Int. J. Hydrogen Energy 34, 8854-8858.
42. Kawai, M., Nagao, N., Tajima, N., Niwa, C., Matsuyama, T., Toda, T., 2014. The effect of
the labile organic fraction in food waste and the substrate/inoculum ratio on anaerobic
digestion for a reliable methane yield. Bioresour. Technol. 157, 174–180.
43. Kim, D.H., Kim, S.H., Jung, K.W., Kim, M.S., Shin, H.S., 2011. Effect of initial pH
independent of operational pH on hydrogen fermentation of food waste. Bioresour.
Technol. 102, 8646-8652.
44. Kiran, E.U., Trzcinski, A.P., Liu, Y., 2015. Enhancing the hydrolysis and methane
production potential of mixed food waste by an effective enzymatic pretreatment.
Bioresour. Technol. 183, 47–52.
45. Kobayashi, T., Xu, K.Q., Li, Y.Y., Inamori, Y., 2012. Effect of sludge recirculation on
characteristics of hydrogen production in a two-stage hydrogen–methane fermentation
process treating food wastes. Int. J. Hydrogen Energy 37, 5602–5611.
46. Kong, X., Wei, Y., Xu, S., Liu, J., Li, H., Liu, Y., Yu, S., 2016. Inhibiting excessive
acidification using zero-valent iron in anaerobic digestion of food waste at high organic
load rates. Bioresour. Technol. 211, 65–71.
47. Kuruti, K., Begum, S., Ahuja, S., Rao Anupoju, G., Juntupally, S., Gandu, B., Kumar
Ahuja, D., 2017. Exploitation of rapid acidification phenomena of food waste in reducing
the hydraulic retention time (HRT) of high rate anaerobic digester without conceding on
biogas yield. Bioresour. Technol. 226, 65–72.
48. Lee, D.-Y., Ebie, Y., Xu, K.-Q., Li, Y.-Y., Inamori, Y., 2010. Continuous H2 and CH4
production from high-solid food waste in the two-stage thermophilic fermentation process
with the recirculation of digester sludge. Bioresour. Technol. 101(1), S42–S47.
49. Li, Y.Y., Jin, Y.Y., 2015. Effects of thermal pretreatment on acidification phase during
two-phase batch anaerobic digestion of kitchen waste. Renew. Energy 77, 550-557.
50. Liu, G., Zhang, R., El-Mashad, H.M., Dong R., 2009. Effect of feed to inoculum ratios on
biogas yields of food and green wastes. Bioresour. Technol. 100, 5103–5108.
51. Liu, X., Wang, W., Gao, X., Zhiu, Y., Shen, R., 2012. Effect of thermal pretreatment on the
physical and chemical properties of municipal biomass waste. Waste Manag. 32, 249-255.
52. Liu, X., Li, R., Ji, M., Han, L., 2013. Hydrogen and methane production by co-digestion of
waste activated sludge and food waste in the two-stage fermentation process: substrate
conversion and energy yield. Bioresour. Technol. 146, 317–323.
53. Lü, F., Hao, L., Zhu, M., Shao, L., He, P., 2012. Initiating methanogenesis of vegetable
waste at low inoculums-to-substrate ratio: importance of spatial separation. Bioresour.
Technol. 105, 169–173.
54. Ma, Y., Yin, Y., Liu, Y. 2017. A holistic approach for food waste management towards
zero-solid disposal and energy/resource recovery, Bioresour. Technol. 228, 56-61.
55. Mata-Alvarez, J., Dosta, J., Romero-Güiza, M.S., Fonoll, X., Peces, M., Astals, S., 2014. A
critical review on anaerobic co-digestion achievements between 2010 and 2013. Renew.
Sustainable Energy Rev. 36, 412–427.
56. Micolucci, F., Gottardo, M., Bolzonella, D., Pavan, P., 2014. Automatic process control for
stable bio-hythane production in two-phase thermophilic anaerobic digestion of food waste.
Int. J. Hydrogen Energy 39, 17563–17572.
57. Montecchio, D., Gallipoli, A., Gianico, A., Pagliaccia, P., Mininni, G., Braguglia, C.M.,
2016. Biomethane potential of food waste: modeling the effects of mild thermal
pretreatment and digestion temperature. Environ. Technol. DOI:
10.1080/09593330.2016.1233293
58. Nagao, N., Tajima, N., Kawai, M., Niwa, C., Kurosawa, N., Matsuyama, T., Yusoff, F.M.,
Toda, T., 2012. Maximum organic loading rate for the single -stage wet anaerobic
digestion of food waste. Bioresour. Technol. 118, 210-218.
59. Naran, E., Toor, U.A., Kim, D.J., 2016. Effect of pretreatment and anaerobic codigestion of
food waste and waste activated sludge on stabilization and methane production. Int.
Biodeterior. Biodegr. 113, 17-21.
60. Nathao, C., Sirisukpoka, U., Pisutpaisal, N., 2013. Production of hydrogen and methane by
one and two stage fermentation of food waste. Int. J. Hydrogen Energy 38, 15764–15769.
61. Nghiem, L.D., Koch, K., Bolzonella, D., Drewes, J.E., 2017. Full scale co-digestion of
wastewater sludge and food waste: Bottlenecks and possibilities. Renew. Sustainable
Energy Rev. 72, 354-362.
1
62. Owamah, H.I., Izinyon, 2015. The effect of organic loading rates (OLRs) on the
performances of food wastes and maize husks anaerobic co-digestion in continuous mode.
Sustainable Energy Technol. Assess. 11, 71–76.
63. Pagliaccia, P., Gallipoli, A., Gianico, A., Montecchio, D., Braguglia, C.M., 2016. Single
stage anaerobic bioconversion of food waste in mono and co-digestion with olive husks:
Impact of thermal pretreatment on hydrogen and methane production. Int. J. Hydrogen
Energy 41(2), 905-915.
64. Pan, J., Zhang, R., El-Mashad, H.M., Sun, H., Ying, Y., 2008. Effect of food to
microorganism ratio on biohydrogen production from food waste via anaerobic
fermentation. Int. J. Hydrogen Energy. 33, 6968-6975.
65. Patinvoh, R.J., Osadolor, O.A., Chandolias, K., Sárvári Horváth, I., Taherzadeh, M.J.,
2017. Innovative pretreatment strategies for biogas production. Bioresour. Technol. 224,
13-24.
66. Paudel, S., Kang, Y., Yoo, Y.-S., Seo, G.T., 2017. Effect of volumetric organic loading rate
(OLR) on H2 and CH4 production by two-stage anaerobic co-digestion of food waste and
brown water. Waste Manag. 61, 484–493.
67. Qiang, H., Niu, Q., Chi, Y., Li, Y., 2013. Trace metals requirements for continuous
thermophilic methane fermentation of high solid food waste. Chem. Eng. J. 222, 330–336.
68. Rafieenia, R., Girotto, F., Peng, W., Cossu, R., Pivato, A., Raga, R., Lavagnuolo M.C.,
2017. Effect of aerobic pre-treatment on hydrogen and methane production in a two-stage
anaerobic digestion process using food waste with different compositions. Waste Manag.
59, 194-199.
69. Rajagopal, R., Bellavance, D., Rahaman, M.S., 2017. Psychrophilic anaerobic digestion of
semi-dry mixed municipal food waste: For North American context. Process Safety and
Environ. Protection 105, 101-108.
70. Ratanatamskul, C., Manpetch, P., 2016. Comparative assessment of prototype digester
configuration for biogas recovery from anaerobic co-digestion of food waste and rain tree
leaf as feedstock. Int. Biodeterior. Biodegrad. 113, 367-374.
71. Redondas, V., Gómez, X., García, S., Pevida, C., Rubiera, F., Morán, A., Pis, J.J., 2012.
Hydrogen production from food wastes and gas post-treatment by CO2 adsorption. Waste
Manag. 32(1), 60–66.
72. Rizwan Haider, M., Zeshan, Yousaf, S., Malik, R.N., Visvanathan, C., 2015. Effect of
mixing ratio of food waste and rice husk co-digestion and substrate to inoculum ratio on
biogas production. Bioresour. Technol. 190, 451–457.
73. Serna-Maza, A., Heaven, S., Banks, C.J., 2014. Ammonia removal in food waste anaerobic
digestion using a side-stream stripping process. Bioresour. Technol. 152, 307-315.
74. Shahriari, H., Warith, M., Kennedy, K.J., 2012. Anaerobic digestion of organic fraction of
municipal solid waste combining two pretreatment modalities e high temperature
microwave and hydrogen peroxide. Waste Manag. 32(1), 41-52.
75. Shahriari, H., Warith, M., Hamoda, M., Kennedy, K., 2013. Evaluation of single vs. staged
mesophilic anaerobic digestion of kitchen waste with and without microwave pretreatment.
J. Environ. Manag. 125, 74–84.
76. Shen, F., Yuan, H., Pang, Y., Chen, S., Zhu, B., Zou, D., Liu, Y., Ma, J., Yu, L., Li, X.,
2013. Performances of anaerobic co-digestion of fruit & vegetable waste (FVW) and food
waste (FW): single-phase vs. two-phase. Bioresour. Technol. 144, 80–85.
77. Tampio, E., Ervasti, S., Paavola, T. et al., 2014. Anaerobic digestion of autoclaved and
untreated food waste. Waste Manag. 34, 370–377. doi:10.1016/j.wasman.2013.10.024.
78. Tawfik, A., El-Qelish, M., 2012. Continuous hydrogen production from co-digestion of
municipal food waste and kitchen wastewater in mesophilic anaerobic baffled reactor.
Bioresour. Technol. 114, 270-274.
79. Ventura, J.-R.S., Lee, J., Jahng, D., 2014. A comparative study on the alternating
mesophilic and thermophilic two-stage anaerobic digestion of food waste. J. Environ.
Science 26, 1274–1283.
80. Voelklein, M.A., Jacob, A., O' Shea, R., Murphy, J.D., 2016. Assessment of increasing
loading rate on two-stage digestion of food waste. Bioresour Technol. 202, 172-180.
81. Wang, X., Zhao, Y., 2009. A bench scale study of fermentative hydrogen and methane
production from food waste in integrated two-stage process. Int. J. Hydrogen Energy 34,
245–254.
1
82. Wang, M., Sun, X., Li, P., Yin, L., Liu, D., Zhang, Y., Li, W., Zheng, G., 2014. A novel
alternate feeding mode for semi-continuous anaerobic co-digestion of food waste with
chicken manure. Bioresour. Technol. 164, 309–314.
83. Wu, L.-J., Kobayashi, T., Kuramochi, H., Li, Y.-Y., Xu, K.-Q., 2016. Improved biogas
production from food waste by co-digestion with de-oiled grease trap waste. Bioresour.
Technol. 201, 237–244.
84. Yan, B.H., Selvam, A., Wong, J.W.C., 2016. Innovative method for increased methane
recovery from two-phase anaerobic digestion of food waste through reutilization of
acidogenic off-gas in methanogenic reactor. Bioresour. Technol. 217, 3-9.
85. Yang, L., Huang, Y., Zhao, M. et al., 2015. Enhancing biogas generation performance from
food wastes by high-solids thermophilic anaerobic digestion: effect of pH adjustment. Int.
Biodeterior. Biodegrad. 105, 153–159.
86. Yeshanew, M.M., Frunzo, L., Pirozzi, F., Lens, P.N.L., Esposito, G., 2016. Production of
biohythane from food waste via an integrated system of continuously stirred tank and
anaerobic fixed bed reactors. Bioresour. Technol. 220, 312-322.
87. Yin, Y., Liu, Y., Meng, S., Kiran, E.U., Liu, Y., 2016. Enzymatic pretreatment of activated
sludge, food waste and their mixture for enhanced bioenergy recovery and waste volume
reduction via anaerobic digestion. Applied Energy, 179, 1131-1137.
88. Yirong, C., Heaven, S., Banks, C.J., 2015. Effect of a trace element addition strategy on
volatile fatty acid accumulation in thermophilic anaerobic digestion of food waste. Waste
Biomass Valorization 6, 1–12.
89. Yong, Z., Dong, Y., Zhang, X., Tan, T., 2015. Anaerobic co-digestion of food waste and
straw for biogas production. Renew. Energy 78, 527-530.
90. Zamanzadeh, M., Hagen, L.H., Svensson, K., Linjordet, R., Horn, S.J., 2016. Anaerobic
digestion of food waste—effect of recirculation and temperature on performance and
microbiology. Water Res. 96, 246-254.
91. Zhang, R., El-Mashad, H.M., Hartman, K., Wang, F., Liu, G., Choate, C., Gamble, P.,
2007. Characterization of food waste as feedstock for anaerobic digestion. Bioresour.
Technol. 98, 929-935.
92. Zhang, Y., Banks, C.J., Heaven, S., 2012. Co-digestion of source segregated domestic food
waste to improve process stability. Bioresour. Technol. 114, 168–178.
93. Zhang, C., Su, H., Tan, T., 2013a. Batch and semi-continuous anaerobic digestion of food
waste in a dual solid–liquid system. Bioresour. Technol. 145, 10–16.
94. Zhang, Z.-L., Zhang, L., Zhou, Y.-L., Chen, J.-C., Liang, Y.-M., Wei, L., 2013b. Pilot-
scale operation of enhanced anaerobic digestion of nutrient-deficient municipal sludge by
ultrasonic pretreatment and co-digestion of kitchen garbage. J. Environ. Chem. Eng. 1, 73-
78.
95. Zhang, C., Su, H., Baeyens, J., Tan, T., 2014. Reviewing the anaerobic digestion of food
waste for biogas production. Renew. Sustain. Energy Rev. 38, 383–392.
96. Zhang, W., Wu, S., Guo, J., Zhou, J., Dong, R., 2015a. Performance and kinetic evaluation
of semi-continuously fed anaerobic digesters treating food waste: role of trace elements.
Bioresour. Technol. 178, 297–305.
97. Zhang, W., Zhang, L., Li, A., 2015b. Anaerobic co-digestion of food waste with MSW
incineration plant fresh leachate: process performance and synergistic effects. Chem. Eng.
J. 259, 795–805.
98. Zhang, J., Lv, C., Tong, J., Liu, J., Liu, J., Yu, D., Wang, Y., Chen, M., Wei, Y., 2016.
Optimization and Microbial Community Analysis of Anaerobic Co-digestion of Food
Waste and Sewage Sludge Based on Microwave Pretreatment. Bioresour. Technol. 200,
253-261.
99. Zhu, H., Parker, W., Basnar, R., Proracki, A., Falletta, P., Béland, M., Seto, P., 2008.
Biohydrogen production by anaerobic co-digestion of municipal food waste and sewage
sludges. Int. J. Hydrogen Energy 33, 3651–3659.
100. Zou, L., Ma, C., Liu, J., Li, M., Ye, M., Qian, G., 2016. Pretreatment of food waste with
high voltage pulse discharge towards methane production enhancement. Bioresour.
Technol. 222, 82-88.
1
Food Waste Volume Temperature Duration VS Methane initial CH4 Initial References
type of batch removal yield F/I (or (%) pH
reactors (%) (L CH4 kg- load)
1
VSfed)
Fig. 1. Composition (%) of Food Waste at household in different regions of the world
1
Table 2. Best semi-continuous performances of single and two-stage anaerobic
digestion systems in terms of methane conversion
FW one or two Tem HRT OLR Durati VS Methane Referenc
type/source stage reactors pera (d) (g VS L-1d- on removal yield es
1
(volume) ture ; kg VS m- (d) (%) (L CH4 kg-1
3 -1
d VSfed)
kitchen 2 (1L; 5L) ther 2;10 N.R. 60 . 364 Chu et
garbage mo/t al., 2012
herm
o
Kitchen 1 (5m3) meso N.R. 3.79 6 months 96 380 Grimb
erg et
al.,
2015
2(5 m3; 5 m3) meso N.R. 0.78 400 93 446
/mes
o
dining hall 2 (8L; 40L) ther 2.87;1 15 78.7 (as 470 Kobay
raw food mo/t 4.4 COD) ashi et
waste herm al., 2012
o
diningh hall 2 (10L; 40L) ther 1.9/7. 39 g COD 100 450.6 Lee et al., 2010
mo/t 7 L-1d-1; 8.4g
herm COD L-1d-1
o
incoming FW 2 (200L;380L ) ther 3.3/12 18.4/4.8 140 476 Micolucc
at the WWTP mo/t .6 i et al.,
herm 2014
o
local waste 1 (3L working meso 16 9.2 45 91.8 455 Nagao et
management volume) al.,2012
comp
synthetic 1 (12 L ther 50 6.3 kg COD 38 72 430±2 Qiang et al.,
working vol) mo m3 day-1 2013
synthetic + 1 (12 L ther 30 6.3 kg COD 120 78 475±95
TEs working vol) mo m3 day-1
FW +fruit 1 (8L) meso 30 1-3.5 210 328-544 Shen et
and vegetable al., 2013
waste
2 (5L; 8L) meso 10/10 1°stage: 2.0 210 198-546
/mes – 10
o 2°stage: 1.0
– 5.0
souce 1 (1L) meso 78 3 100 77.7 483 ±13 Tampio et
segregated al., 2014
domestic
food waste
food waste 2 (10L;30L) Mes 5.0/15 3.2 195 78.5 380 Ventura
recycling o/me et al.,
company so 2014
2 (10L;30L) Mes 5.0/15 4.4 109 81.7 440
o/ter
mo
2 (10L;30L) ther 5.0/15 4 43 79.2 370
mo/
meso
local waste 2 (5L; 5L) meso 4/12 15;5 N.R. 389.2±31.8 Voelklei
management /mes n et al.,
comp o 2016
1 (5L) meso 16 4 N.R. 316.4 ± 17.9
restaurant 2 (450L; 40°C 160h( 22.65; 4.61 125 546 Wang
1500L) /40° SRT); and
C 26.67d Zhao,
2009
synthetic 2 (1.6 CSTR; ther 3.7/1. 3.4/6.1g 30 334.7* Yeshane
1.3 AFBR; mo/ 5 COD L-1d-1 w et al.,
with meso 2016
recirculation)
1
source segregated 1 (5L) ther N.R. 2 50 400 Yirong et
domestic FW mo al., 2015
(with TEs)
pasteurized 1 (10L) meso 20 3 152 480 Zaman
±33 zadeh
et al.,
2016
1(10L) ther 20 3 152 448
mo ±44
canteen 1 (1L) meso 25 7 N.R. 405 Zhang et al.,
2013a
campus 1(6L) meso 40 4.5 22 460 Zhang
restaurant et al.,
(with TEs) 2015a
CSTR: continuous stirred tank reactor; AFBR anaerobic fixed bed reactor; N.R.:not reported; *in L CH4
kg-1 COD d-1
1
Table 3. Best operating conditions and hydrogen yields from food waste fermentation,
in single and dual stage.
Single-Stage
Inoculu Operative conditions
m Reactor Tempera HRT Organ pH Durati Referen
Inoculu
Waste Pre- type ture (°C) (h) ic on H2 Yield ces
m
treatme Load
nt
Mesophil
ic
39 mL g-
anaerobic 1
35 NR S/I: 6 44 h VSfed
sludge Pan et
FW - Batch NR
Thermop al., 2008
55 NR S/I: 7 44 h 57 mL g-
hilic 1
VSfed
anaerobic
sludge
Heat 219.9 mL g-
1
FW pretreat VSfed
Anaerobi Batch Han et
hydrolys ment 37 NR NR 4.0 - 4.6 75 d (1.56 mol
c sludge (0.5 L) -1 al., 2015
ate (T=100° mol glucose
C; t=6 h) added)
Heat
Initial
pretreate
pH:8 1.92 mol mol-
d FW Batch 1 Kim et
None - 35 NR NR Operati 100 h hexose
(T=90°C; (0.2 L) al., 2011
onal added
t=20
pH:5
min);
162 mL g-
Alkali 1
VSfed
pretreate Batch Jang et
None - 37 NR NR 6.0 1.2 d (1.71 mol
d FW (0.3L) al., 2015
mol-1 hexose
(pH:12)
added)
Heat
FW Max 149 mL
pretreat 4
(ultrasou Batch g-1VSfed
Anaerobi ment gCOD Gadhe et
nd pre- (0.125 37 NR 5.5 NR (FW
c sludge (T=90°C g- al., 2014
treatment L) 1 TS=8%;USti
; t=20 VSS
) me:15 min)
min)
80.6 mL g-
1
COD
(2.8% T80)
FW
Heat 70:30 82.4 mL g-
(pretreat 1
pretreat % COD
ment Batch Elsamad
Sewage ment (v/v) (1.7 g L-1
with T80 (0.18 55 NR NR 60 h ony et
sludge (T=100° 22.6 PEG)
and L) al., 2015
C; t=15 (VS/V 85.6 mL g-
PEG6000
min) S)a 1
COD
)
(2.8%
T80+1.7 g L-1
PEG)
Incline
Heat
d plug
pretreat
flow 8.19 Jayalaks
Kitchen Digested ment HRT:1 72 mL g-
reactor n.r. gVS 5.6 NR hmi et
waste slurry (T=100° 68a 1
VSfed
(150 L) L-1d-1 a al., 2009
C; t=30
pilot
min)
scale
OFMSW
Elbeshbi
(ultrasoni
Batch Initial 118 mL g- shy et
c + acid None - 37 NR NR 360 h 1
(0.2 L) pH:5.5 VSfed al., 2011
pretreate
a
d)
CSTR
Ultrason with
ic pre- ultraso
Elbeshbi
treatmen nic 14.5
Anaerobi 332 mL g- shy et
OFMSW t probe 37 24 gVSS 5-6 45 d 1
c sludge VSSfed al., 2011
(Espec=79 (2 L) L-1d-1
b
kJ kg- continu
1
TS) ous
mode
UASB
Municipa
reactor 29 245 mL g- Tawfik
l food 1
sludge ABR 38.4 gCOD CODremoved and El-
waste+ - 35 -1 - 5.0 - 5.2 250 d
for H2 (26 L) (1.6 d) tot L d 558 mL g- Qelish,
kitchen 1 1
productio VSremoveda 2012
waste
n
1
CSTR
(3 L)
11.4 Redonda
Acidogen Semi- 10 20.5 mL g-
FW - 34 48 gVS 5.5 1 s et al.,
ic sludge continu HRT VSfed
L-1d-1 2012
ous
mode
Table 3. Continue
Operative conditions
Inoculum
Waste Inoculum Reactor type Temperature HRT (h) Organic Load pH
Pre-treatment
(°C)
CMISR (3.2 L)
WWTP packing ratio:15% 40 kgVS m-3d-1
FW hydrolysate Aeration (30 d) NR 6 ˃4
sludge of activated 16 kgVS m-3d-1
carbon
SRT:45.6
FW + OFMSW (20:80) No - SSRT 55 66 gVS L-1d-1 5.54
(1.9 d)
Anaerobic
FW - CSTR (4.5 L) 55 120 23.6 kgCOD m-3d-1 NR
sludge
Two-Stage
FW No - SCRD (200 L) 40 SRT:160 22.65 kgVS m-3d-1 5.6 - 5.
Heat pretreatment
Anaerobic Semi-continuous 45.6
FW (T=90°C; t=30 min) + 55 39 (gCOD L-1d-1) 5.4 - 5.
sludge reactor (10 L) (1.9 d)
acclimatization
Heat pretreatment
Anaerobic Semi-continuous 68.9
FW (T=90°C; t=30 min) + 55 NR 5.4-5.6
sludge reactor (8 L) (2.87 d)
acclimatization
Anaerobic Heat pretreatment CSTR (1 L)
Kitchen garbage 55 2d NR 5.5
sludge (T=70°C; t=30 min) Semi-continuous
Full scale Two stage batch
Heat pretreatment
FW UASB reactor fermentation 37 NR S/I : 7.5 Initial pH
(T=90°C; t=30 min)
sludge (0.5 L)
Source-segregated FW WWTP
CSTR (1 L)
(+2nd phase recycled mesophilic - 52 72 20 gVS L-1d-1 5.22
Semi-continuous
sludge) digestate
Mesophilic CSTR (5 L)
FW anaerobic - semi continuous 35 10 2 gVS l-1 d-1 NR
sludge mode
nd
OFMSW (+2 phase CSTR (200 L) 79.2
No - 55 18.4 kgVS m-3d-1 5.2
recycled sludge) Semi-continuous (3.3 d)
Heat pretreatment
Anaerobic (T=120°C; t=20 min) CSTR (1.35 L) 9 gVS L-1d-1
Source-segregated FW 35 96 5.5
sludge + 1 M HCl + Semi-continuous (tested range 6-15)
acclimatization (20 d)
Anaerobic CSTR (1.6 L) 88.8
FW - 55 3.4 gVS L-1d-1 5.0 - 5.
sludge Semi-continuous (3.7 d)
FW (no pretreatment) UASB
Heat pretreatment
FW (aeration pretreatment; granular Batch (1 L) 35 NR S/I: 0.3 6.0
(T=80°C; t=15 min)
air flow = 5L h-1; t=24 h) digestate
ABR: anaerobic buffled reactor; CSTR: continuous stirred tank reactor; CMISR: continuous mixed
immobilized sludge reactor; SCRD: semi-continuous rotating drum;
SSRT: semi-continuous stirred tank reactor; UASB: upflow anaerobic sludge blanket reactor; NR: Not
reported; v/v = volume/volume
a
Calculated
1
Table 4. Operative conditions and anaerobic performances of co-digestion of food waste
with other substrates
FW + Animal Waste
Co- Pretreatme Process Operative conditions Performances References
substrates nt type
(Shredding Tem HRT OLR or Duration VS CH4 H2
excluded) p (d) S/I (d) remov yield yiel
(°C) al (L d
(%) CH4 (L
kg- H2
1
VS) kg-
1
VS
)
FW+PMa None Batch (0.5 37 - S/I = 3 35 NR Dennehy et
(VS ratio) L) (VS 54% 320 al., (2016)
(20/80) based) 63% 443
(40/60) 68% 489
(60/40) 71% 521
(80/20)
FW+DMb None Batch (1 L) 35 - Initial 30 NR El-Mashad
(VS ratio) loading 60% 282 and Zhang
(32/68) =3 gVS 68% 311 (2010)
(48/52) L-1
FW+DMb None CSTR (2 L) 36 80 2 gVS 180 NR 630 NR Agyeman
(VS ratio) L-1 d-1 (fine- and Tao
(50/50) grinde (2014)
d FW)
470
(coars
e-
grinde
d FW)
FW+ChMc None CSTR (3.5 35 35 2.5 gVS 225 NR 508 NR Wang et al.,
(Alternate L) L-1 d-1 (2014)
feeding)
FW+CSf (VS None CSTR (75 36 30 2 gVS 308 NR 220 NR Zhang et al.,
ratio) L) L-1 d-1 (2012)
(20/80)
FW+CMd None Induced 55 20 5.53 40 82.5% 330 NR Castrillón et
(w/w) Bed gCOD al. (2013)
(10/90) Reactor (19 L-1 d-1
L)
FW+CoMg None SBR (24 L) 20 NR 0.8–4.2 205 NR 477 ± NR Rajagopal et
(NR) gVS L-1 (Cycle 88 al. (2017)
d-1 length=7 (last
d) 24
cycles)
FW + Sewage Sludge
FW+PSh+W None Batch (0.1 NR - S/I = 4 NR NR NR Zhu et al.
ASi (v/v) L) (Volum 104 (2008)
(75/12.5/12.5 e based) 112
) 10
(50/25/25)
(25/37.5/37.5
)
FW+SSj (TS Batch (0.4 37 - S/I = 5 35 NR Zhang et al.,
ratio) None L) (TS 50% 297 (2016)
(50/50) Microwave based) 48.1% 311
(50/50) s
FW+WASi None Two-stage 37 - S/I = 2.3 55 18% - - 25 - Liu et al.,
(w/w) batch - S/I = 3.0 (hours) 50% 216 - 106 (2013)
(Several tests (0.1 L) (VS 1000 22% - 354 -
with FW based) (hours) 32%
contents =
10%; 20%;
30%; 40%;
54%; 85%)
FW+WASi None CSTR (2 L) 16.7 2 gVS NR Gou et al.,
(TS ratio) 35 d L-1 d-1 160 d 62% 250 (2014)
(33.3/66.6) 45 178 d 60% 290
(33.3/66.6) 55 188 d 58% 370
(33.3/66.6)
FW+DSk (VS None CSTR (6 L) 35 20 NR NR Dai et al.,
ratio) 6.3 gVS 46% 258 (2013)
(30/70) L-1 d-1 58% 332
(50/50) 7.2 gVS 67% 380
1
(70/30) L-1 d-1
7.6 gVS
L-1 d-1
FW+WASi None Single-stage 35 20 0.85 350 46% 960 NR Zhang et al.,
(VS ratio) pilot CSTR gVS L-1 (bioga (2013b)
(16.5/83.5) (20 tonns) d-1 s)
FW+WASi None Two-stage 35 NR NR 350 48% 440 NR
(VS ratio) pilot CSTR (bioga
(16.5/83.5) (4.5+15.5 s)
tonns)
FW + Green and Agro/Waste
FW+OHl None Batch (0.3 37 - S/I = 0.6 30 49% 505 84 Pagliaccia et
(w/w) Thermal L) (VS 53% 91 87 al., (2016)
(67/33) based)
FW+GWm None Batch (1 L) 50 - S/I = 1.6 25 90.8% 430 NR Liu et al.,
(VS ratio) 50 S/I = 3.1 82.5% 359 (2009)
(50/50) 50 S/I = 4.0 80.8% 390
50 S/I = 5.0 60.2% 337
35 S/I = 3.1 48.7% 185
(VS/VS
S based)
FW+Sn None Batch (1 L) 35 - Initial NR NR NR Yong et al.,
(w/w) loading 171 (2015)
(20/80) =5 gVS 299
(60/40) L-1 313
(80/20)
FW+RHo None Batch (1 L) 37 - S/I = 45 55% 557 NR Rizwan
(VS ratio) 0.25 48% (bioga Haider et
(98/2) S/I = 0.5 31% s) al., (2015)
S/I = 1.0 27% 458
S/I = 1.5 24% (bioga
S/I = 2.0 s)
(VS 267
based) (bioga
s)
97
(bioga
s)
71
(bioga
s)
FW+MHp None CSTR (5 L) 37 68 1 gVS 120 80.7% 400 NR Owamah
(w/w) 27 L-1 d-1 120 76.5% 408 and Izinyon
(75/25) 19 2.5 gVS 120 74.3% 447 (2015)
15 L-1 d-1 120 78.3% 482
3.5 gVS
L-1 d-1
4.5 gVS
L-1 d-1
FW+FVWq None One-stage 35 30 Single 210 NR 328 - - Shen et al.
(VS ratio) CSTR (8 L) 10 stage: 140 544 5- (2013)
(81/19) Two-stage 10 1.0 – 3.5 210 - 28
CSTR (5 L gVS L-1 198 - -
+ 8 L) d-1 546
1°stage:
2.0 – 10
gVS L-1
d-1
2°stage:
1.0 – 5.0
gVS L-1
d-1
FW+RTLr None Pilot scale 35 30 6.8 gVS 112 80.4% 153 NR Ratanatams
(w/w) one stage L-1 d-1 kul and
(95/5) (2500 L) 30 89.2% 283 Manpetch
Pilot scale 9.5 gVS (2016)
two stage L-1 d-1
(1000 L +
2500 L)
FW+LWs None High Solids 35 175 2 gCOD 141 NR 229 NR Drennan and
(FW and LW Digester (SR L-1 d-1 DiStefano
mixed to (280 L) T) (2014)
obtain
constant
OLR and
reactor
TS=20%)
FW+RHo None Pilot scale 37 26 5 gVS 27 82.4% 446 NR Jabeen et al.
(mixed to Plug-Flow 25 L-1 d-1 52 73.1% (bioga (2015)
obtain a (80 L) 14 6 gVS 30 35.4% s)
1
C/N=28) L-1 d-1 399
9 gVS (bioga
L-1 d-1 s)
215
(bioga
s)
FW + Other Waste
FW+GTWu None CSTR (6 L) 35 30 NR 180 77.4% 620 - Wu et al.
(NR) TPADx (10 55+3 6+24 73.3% 520 - (2016)
L) 5 3+12 78.8% 470 13.
TPADry 55+3 5
(7.5 L) 5
FW+BWv None Acidogenic 35 2 18 gVS 47 29% - 78. Paudel et al.
(v/v) CSTR (8 L) 35 1 L-1 d-1 34 27% - 5 (2017)
(70/30) 35 0.5 35 gVS 27 26% - 73.
35 0.33 L-1 d-1 25 NR - 6
Methanoge 35 20 71 gVS 70 52.5% 728 80.
nic 35 15 L-1 d-1 80 44% 676 5
CSTR (30 106 99.
-1
L) gVS L 8
d-1 -
1.24 -
gVS L-1
-1
d
1.76
gVS L-1
d-1
w
FW+FIL None CSTR (0.3 37 20 4.1 gVS 70 78% 479 - Zhang et al.
(VS ratio) L) 15 L-1 d-1 70 76% 452 - (2015b)
(77/23) 10 6.2 gVS 70 72% 506 -
L-1 d-1
8.3 gVS
L-1 d-1
a
PM= Pig Manure; DM=Dairy Manure; ChM=Chicken Manure; dCM=Cattle Manure; eSS=Sewage Sludge;
b c
f
CS=Cattle Slurry; gCoM=Cow Manure;
h
PS=Primary Sludge; iWAS=Waste Activated Sludge; jSS=Sewage Sludge; kDS=Dewatered Sludge; lOH=Olive Husk;
m
GW=Green Waste;
n
S=Straw; oRH=Rice Husk; pMH=Maize Husk; qFVW=Fruit and Vegetable Waste; rRTL=Rain Tree Leafs;
s
LW=Landscape Waste;
t
OFMSW=Organic Fraction of Municipal Solid Waste; uGTW=De-oiled Grease Trap Waste; vBW=Brown Water;
w
FIL=Fresh Incineration plant Leachate;
x
TPAD=Temperature Phased Anaerobic Digestion; yTPADr=TPAD with biomass recycling.
NR=Not Reported; S/I=Substrate/Inoculum ratio; w/w = weight/weight; v/v = volume/volume.
1
Table 5. Pre-treatment impact on solubilization and anaerobic digestion performances
Type Su Pretreatment Pretre Process type and Solubilisation Result Refer
bst method atmen parameters s ences
rat t
e conditi
ori ons
gin
Sou Autoclave T=160 T=37°C; F/I=1 (VS); +16% sCOD, +22% NH4-N 445 Tampi
rce °C; Working volume= 0.4 L; mLCH o et
seg p=6.2 Duration= 35 days 4/gVSfe al.,
reg bars d vs 2014
ate 501
d mL
do CH4/g
mes VSfed (-
tic 11%)
FW
Caf Autoclave T T=37°C; F/I=0.6 (VS); pHi +35% sCOD,+75% soluble sugars**; 23 Paglia
eter max=1 set to 7 Working volume +58% soluble proteins** mLH2/ ccia et
ia 34°C; =0.3 L; Duration= 30 days gVSfed al.,
foo p vs 5 2016
d max=3 mLH2/
was .2 bar; gVSfed
te Retenti (+360
on %);
time= 385
20 min mLCH
4/gVSfe
d vs
446
mLCH
4/gVSfe
d (-
14%)
Uni Autoclave T T=35°C; Load= 0.8 gVS; +27% sCOD, +19% soluble sugars 39.2 Hu et
ver max=1 No inoculum addition; mLH2/ al.,
sity 21°C; Working volume = 0.03 L; gVSfed 2014
Can Retenti Duration= 5 days; vs 0.4
tee on mLH2/
THERMAL
n time= gVSfed
BATCH
15 min **
(+9700
%)
Kit Thermal T=120 T=35°C; 2 phase system; 899 Li and
che °C; Working volume mLCH Jin,
n Retenti acidogenic= 5.5 L; 4/gVSfe 2015
was on Duration= 21 days; d ** vs
te time= 607mL
50 min CH4/g
VSfed
**
(+48%
)
Kit Thermal T=175 T=35°C; F/I= 0.2;pHi set to +114% soluble sugars **, +204% soluble -7.9% Liu et
che °C; 7.5;Working volume= 0.25 proteins ** (kitchen waste); +312% on al.,
n Retenti L; Duration= 15 days; soluble sugars **, +185% soluble methan 2012
was on proteins ** (vegetable/fruit residue) e yield
te; time= mLCH
veg 60 min 4/gVSfe
eta d
ble/ (kitche
frui n
t waste);
resi -11.7%
due on
methan
e yield
mLCH
4/gVSfe
d
(vegeta
ble/frui
t
residue
)
1
Syn Thermal T=80° T=33°C; F/I= 0.5 (VS); 647 Ariun
thet (various) C; Working volume= 1 L; mLCH baatar
ic Retenti Duration= 220 days; 4/gVSfe et al.,
foo on d vs 2014
d time= 426
was 90 min mLCH
te 4/gVSfe
d
(+52%
)
Din Microwave Micro T=37°C; F/I=5 (TS); Co- -25% sCOD **, -52% soluble sugars **, 316 Zhang
ing wave digestion with sewage +45% soluble proteins** mLCH4/ et
hall freque sludge (ratio FW:SS=3:2 gVSfed al.,20
ncy= TS based) Working (ratio 16
2450 volume= 0.4 L; Duration= MW-
MHz; 35 days FW:SS
Ambie 3:2) vs
nt 71
pressur mLCH4/
e; gVSfed
Power (only
= FW)
600W; (+347
Tmax=1 %)
00°C;
No
retenti
on
time
M- Microwave Micro T=33°C; Working volume= +21% sCOD **, +12.5% soluble proteins +8% Shahri
OF wave 0.155 L; Duration= 30 ** on total ari et
MS freque days* biogas al.,
W ncy= produc 2012
(rep 2450 tion **
rese MHz;
ntat Tmax=1
ive 15°C;
of Ramp
Can time=
adi 40
an min;
kitc Retenti
hen on
was time=
te) 1 min
Camp Ultrasounds Pow T=37° +7% sCOD 48 Gadhe et
us er= C; F/I= mLH2/gVSfed al., 2014
cafete 1200 4 vs 15
ria W; (COD/ mLH2/gVSfed
Freq VSS); (220%)
uenc pHi set
y= to 5.5;
20 Worki
kHz; ng
Tmax volum
= e=
30° 0.125
C; L;
Rete
ntio
MECHANICAL
n
time
= 15
min
Food Ultrasounds Ener T=35° 206 Naran et
waste (various) gy C; F/I mLCH4/gVS al., 2016
treatm inten (VSS) Sremoved vs
ent sity = 137
plant = 60**; mLCH4/gVSr
7300 Worki emoved (+50%)
KJ/k ng
gTS vol=
S**; 0.06 L;
Rete Durati
ntio on= 20
n days
time
= 30
min
1
Unive HVPD (High Puls T=35° +16% sCOD, +53% soluble sugars, +1149% soluble 315 Zou et al.,
rsity Voltage e C; proteins (40kV, 5mm, 300Hz, 30 min); +107% mLCH4/gCO 2016
Cante Pulse volta F/I=0.5 sCOD, +25% soluble sugars, +171% soluble proteins Dremoved vs
en Discharge); ge= (VS); (34kV, 5mm, 400Hz, 30 min) 234mLCH4/g
(various) 40k pHi set CODremoved
V; to 7; (+35%).
Elec Worki
trod ng
e volum
dista e= 1 L;
nce= Durati
5m on= 45
m; days *
Puls
e
freq
uenc
y=
400
Hz;
Rete
ntio
n
time
=
30m
in
Unive Enzymatic Gluc T=35° +1547% sCOD*,** 468 Kiran et
rsity hydrolysis oam C; F/I= mLCH4/gVSf al., 2015
Cafete ylas 0.5 ed vs 198
ria e gVS/g mLCH4/gVSf
loadi VSS** ed (+137%)
ng= ;
10 Worki
U/gd ng
ryF volum
W e= 0.3
T= L**;
60° Durati
C; on= 30
cont days;
act
time
=
24h
Unive Enzymatic Gluc T=35° +25% sCOD*,** 817 Yin et al.,
rsity hydrolysis oam C; F/I= mLCH4/gVSf 2016
Cante ylas 5 ed vs 610
en e (TS/V mLCH4/gVSf
BIOLOGICAL
z;
Tmax
=
85°
C;
Ram
p
time
= 40
min;
Rete
ntio
n
time
=1
min;
Organ Ultrasounds Pow T=37° +30% sCOD *,**; +31% soluble sugars; +35% 118 Elbeshbish
ics with acid er= C; soluble proteins *,** mLH2/gVSfed y et al.,
Proce (various) 500 No vs 42 2011a
ssing W; inocul mLH2/gVSfed
Facilit Freq um (+181%)
y uenc additio
y= n;
20 pHi set
kHz; to 5.5;
Tma Worki
x= ng
1
30° volum
C; e= 0.2;
spec Durati
ific on= 15
ener days *
gy
inpu
t=
7900
kJ/k
gTS;
pHfi
n=
3.0
(1N
HCl)
;
Cont
act
time
=
24h
at
4°C
Sourc Autoc T=16 T=37°C; +16% sCOD, +22% NH4-N 439 mLCH4/gVSfed vs 465 Tampio et
e lave 0°C; OLR=4 mLCH4/gVSfed (-6%) al., 2014
segre p=6.2 kgVS/m3·
gated bars d; HRT=
dome 47 d (Untr
stic 58d);
FW duration=
162 days
**;
Working
volume=
11 L
Synth Micro Micro T=35°C; +19% sCOD** 1.50 LCH4/L·gVSremoved·d vs 1.31 Shahriari et
THERMAL
2.7°C 7d;
/min Working
volume=
0.3/0.6L
Duration=
20d *;
Orga Ultras
Power T=37°C; +9% sCOD, +17% soluble 247 mLH2/gVSSfed vs 180 Elbeshbishy
nics ounds
= 500 CSTR sugars, +20% soluble proteins mLH2/gVSSfed (+37%) et al., 2011b
Proce W; reactor
ssing Frequ (HRT= 2
Facili ency= days;
ty 20 OLR=
kHz; 14.5 for
Tmax untreated
= and 13.4
MECHANICAL
30°C; gVSS/L·d
Specif for
ic sonicated);
energ Working
y volume =
input 2 L;
= Duration=
5000 45 days;
kJ/kg
TS;
Reten
tion
time=
24
min
* deducted from the graph; ** calculated
1
More than 400 papers in the last 5 years have been published on FW into energy
Food waste complexity and composition affects anaerobic conversion
Scaling up of the AD process is fundamental to assess the real methane potential
Methanogenesis is often rate limiting step leading to pH drop and instability
Strategies to improve AD performances and stability are here reviewed