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Review

Nitrogen Removal from Mature Landfill Leachate via Anammox Based Processes: A Review

1
Centre for Urban Environmental Remediation, Beijing University of Civil Engineering and Architecture, Beijing 100044, China
2
Beijing Energy Conservation & Sustainable Urban and Rural Development Provincial and Ministry Co-Construction Collaboration Innovation Center, Beijing University of Civil Engineering and Architecture, Beijing 100044, China
*
Author to whom correspondence should be addressed.
Sustainability 2022, 14(2), 995; https://doi.org/10.3390/su14020995
Submission received: 17 December 2021 / Revised: 7 January 2022 / Accepted: 10 January 2022 / Published: 17 January 2022
(This article belongs to the Collection Sustainability of Water Environment)

Abstract

:
Mature landfill leachate is a complex and highly polluted effluent with a large amount of ammonia nitrogen, toxic components and low biodegradability. Its COD/N and BOD5/COD ratios are low, which is not suitable for traditional nitrification and denitrification processes. Anaerobic ammonia oxidation (anammox) is an innovative biological denitrification process, relying on anammox bacteria to form stable biofilms or granules. It has been extensively used in nitrogen removal of mature landfill leachate due to its high efficiency, low cost and sludge yield. This paper reviewed recent advances of anammox based processes for mature landfill leachate treatment. The state of the art anammox process for mature landfill leachate is systematically described, mainly including partial nitrification–anammox, partial nitrification–anammox coupled denitrification. At the same time, the microbiological analysis of the process operation was given. Anaerobic ammonium oxidation (anammox) has the merit of saving the carbon source and aeration energy, while its practical application is mainly limited by an unstable influent condition, operational control and seasonal temperature variation. To improve process efficiency, it is suggested to develop some novel denitrification processes coupled with anammox to reduce the inhibition of anammox bacteria by mature landfill leachate, and to find cheap new carbon sources (methane, waste fruits) to improve the biological denitrification efficiency of the anammox system.

1. Introduction

With urbanization, population growth and industrialization, the amount of municipal solid waste has increased sharply, and landfill is the most common way to dispose solid waste, but this has also led to the production of a large amount of landfill leachate [1]. The special characteristics of landfill leachate, including high age dependent concentrations of ammonia, refractory organic matter and heavy metal ions, can potentially have hazardous and toxic effects on the environment and endanger human health [2].
Landfill leachate, especially mature landfill leachate, is difficult to treat using conventional biological processes. As the landfill time increases (>10 years), organic nitrogen in the leachate is gradually converted to ammonia nitrogen, while the organic matter, especially the bioavailable part, decreases, forming mature landfill leachate characterized by high ammonia nitrogen, low C/N, and (Biochemical Oxygen Demand) BOD5/(Chemical Oxygen Demand) COD [3]. So far, there are many ways to treat landfill leachate, mainly physiological–chemical processes and biological methods. At present, ion exchange, reverse osmosis, advanced oxidation, ammonium stripping and chemical precipitation have been commonly used to treat mature landfill leachate [4,5,6]. Although the physic–chemical processes described above can remove most of the toxic and harmful substances in mature landfill leachate, they are expensive and produce secondary pollution, and the physic–chemical process usually needs to be used in combination with biological methods [7]. In contrast, biological treatment is widely used in the denitrification of mature landfill leachate due to its high economic benefits [2]. In practical application, the traditional nitrification and denitrification process is one of the most commonly used biological denitrification technologies, such as the conventional activated sludge process, moving bed biofilm reactor (MBBR) biological filter and sequencing batch reactors (SBR) [8]. However, the process has some disadvantages in long term operation, such as high aeration energy consumption, large greenhouse gas production, the high cost of an external carbon source and large floor area, which restricts its further popularization and application. Especially in mature landfill leachate, COD/N and BOD5/COD ratios are low, which is not suitable for the nitrification and denitrification process [9].
As a new nitrogen removal process, the anammox process can directly reduce ammonia nitrogen to nitrogen with nitrite nitrogen as an electron donor. Currently, the process has been widely used to treat high ammonia nitrogen wastewater, such as sludge digestion wastewater, semiconductor wastewater, and mature landfill leachate [10,11]. Compared to traditional nitrification–denitrification processes, the anammox process has the merit of saving the carbon source and aeration energy.
Anammox as a single process for nitrogen removal has been developed and attracted much attention. Granular sludge systems or biofilm systems, or a one stage system or multistage system, all have applied in treating mature landfill leachate. The sidestream anammox process has been applied in engineering and more than 100 high ammonia wastewater treatment plants have been established [12]. Although the anammox process is considered to be the suitable treatment method for mature landfill leachate with the highest economic value, there are still some difficulties in its practical application. Firstly, anammox bacteria (AnAOB) are autotrophic bacteria with a long doubling time and need a sufficient nitrogen load, which prolongs the anammox process start up [13]. Secondly, theoretically, 11% of the nitrate produced in the anammox process leads to the failure of the effluent total nitrogen, which means that the effluent needs to be further treated. Lastly, the components of leachate are complex, and its endogenous substances have positive or negative effects on the anammox process [14,15]. In order to solve these problems, many studies have optimized the process and obtained a series of excellent experimental results, including good nitrogen removal performance.
In this review, the anammox processes for treating mature landfill leachate were reviewed, including the characteristics and operating efficiency of each process. Then, the relevant functional microorganisms and several challenges in real application were systematically introduced. Finally, the effective ways to achieve a high nitrogen removal performance and economic benefit in the future are pointed out. This review is aimed to serve as a guide for future research and the application of anammox processes in the treatment of mature landfill leachate.

2. Mature Landfill Leachate Treatment via Anammox-Based Processes

At present, the anammox based processes for the treatment of mature landfill leachate mainly includes the following three types: partial nitrification–anammox, the coupling of partial nitrification–anammox and denitrification, and the coupling of partial nitrification–anammox and partial denitrification. Every type of process has their own characteristic and nitrogen removal pathway, as shown in Figure 1.

2.1. Partial Nitrification–Anammox Process

The anammox process is a promising technique to treat mature landfill leachate. When treating wastewater, anammox cannot work alone, because it needs the nitrite substrate supplied by nitritation [16]. Stable partial nitrification (PN) is hard to achieve in municipal wastewater treatment due to the dominancy of nitrite-oxidizing bacteria (NOB) over ammonia-oxidizing bacteria (AOB). Various studies have investigated high free ammonia (FA), free nitrous acid (FNA), low dissolved oxygen (DO), and high pH to inhibit NOB growth. The high ammonia nitrogen concentration in landfill leachate can naturally provide enough high FA concentration [3]. The single or two stage partial nitritation–anammox (PN/A) processes are two types of deammonification reactors which were widely used in application. The former is more economical because of its lower civil engineering cost. However, the two stage PN/A process can be preferred for landfill leachate [17]. In this configuration, the COD in the pretreated effluent will preferentially enter the PN reactor to avoid the direct impact of organic matter on AnAOB, subsequently providing a more suitable influent for the following anammox reactor. Compared to one stage PN/A, two stage is advantageous due to the high nitrogen removal rate [18]. A combined continuous flow process of nitritation and anammox produced a total nitrogen volumetric load of anammox in an UASB reactor that was increased from 0.5 kg N/(m3·d) to 1.2 kg N/(m3·d) [19]. In addition, a two-stage anammox SBBR system has been used to treat leachate: after 107 days of operation, the effluent TN remained below 20 mg/L with 95% of TN removed [20].
The single stage PN/A needs more precise control parameters in engineering applications under the conditions of varying influent composition [21]. Numerous studies have investigated PN/A to ensure system stability via DO and COD optimization. One study has investigated the effect of influent organics on an anammox reactor in treating mature landfill leachate, they find influent COD should be maintained below 800 mg/L. Simultaneous denitrification and anammox processes can happen in the system under an appropriate COD concentration, which will enhance the nitrogen removal efficiency and operational stability. The effect of DO on nitrogen removal is also very crucial. Especially in one stage PN/A, the optimum microaerobic conditions can greatly promote the activities of AOB, anammox, and out select NOB. When DO increases from 0.2 mg/L to 0.6 mg/L, the nitrogen removal rate (NRR) decreased by about 20%, owing to the fact that anammox activity was inhibited under the conditions of DO 0.6 mg/L [22]. However, the activity of AOB might also be restricted by low DO. A novel partial nitrification–anammox biofilm reactor (PNABR) operated under high DO concentrations (>1 mg/L) with a preanoxic—aerobic—anoxic operational way has been proposed, where aerobic biofilm was specially cultivated on the outside surface of the anammox bacteria biofilm carrier. Such a configuration enhanced the microbial resistance to high DO conditions. Eventually, NRR and nitrogen removal efficiency (NRE) finally reached 0.396 kg N/(m3·d) and 96.1%, respectively [23]. It is possible that the high ammonia nitrogen content (>1000 mg/L) in mature landfill leachate is another key factor in the inhibition of NOB at high DO.

2.2. Coupling of Partial Nitrification–Anammox and Denitrification

In PN/A processes, 11% of nitrate nitrogen byproducts were generated, which limits the improvement of total nitrogen removal efficiency [24]. Indeed, the organic matter of leachate can be degraded by employing specific heterotrophic bacteria. Therefore, the coupling system of denitrification and PN/A can solve the above problems [25]. There are two coupling types: denitrification (DN) direct coupling in partial nitrification (PN)-anammox (DN + (PN-anammox)) and pre-DN followed by PN-anammox (DN-PN-anammox). DN+ (PN-anammox) have the advantage of saving reactor space, but the disadvantage is that heterotrophic bacteria have more affinity for oxygen, which first oxidized COD with oxygen, and then ammonia oxidation occurred, increasing the energy consumption of the PN section. In contrast, pre-denitrification can utilize influent carbon sources, thus avoiding the inhibition effect of organic matter on AnAOB [26]. To sum up, the combined system can achieve above 87.9% nitrogen removal efficiency, as seen in Table 1. COD removal efficiency ranged from 30% to 60%, although the effluent cannot meet COD discharge standards [27,28]. The percentage of the denitrification contribution to NO3-N removal decreased with higher influent organics loads, this shows the refractory organic matter in mature landfill leachate might serve as the potential electron donor for denitrification, also, they could inhibit denitrification activities. Humic acid (HA) is the dominant soluble DOM with low biodegradability in mature landfill leachate, usually accounting for 4~44% of the total organic carbon (TOC) [29]. HA could suppress the anammox bacteria activity at a certain concentration. Nevertheless, the nitrogen removal efficiency of the system rapidly returned after a short adaptation period. Controlling the abundance of Nitrospirae was the key to further improving the nitrogen removal performance of the system under HA stress. Another major drawback of the process is limited denitrification. The biochemical oxygen demand (BOD) value in mature landfill leachate is low, which limits the synergistic removal performance of carbon and nitrogen during the heterotrophic denitrification process. Concludingly, a step feed partial nitrification and simultaneous anammox and denitrification (SPNAD) process has been proposed, providing sufficient electron donors for the denitrification stage, with a final nitrogen removal efficiency of 98.7% at a total nitrogen removal load of 0.23 kg N/(m3·d) [30].

2.3. Coupling of Partial Nitrification–Anammox and Partial Denitrification Process

NO3-N can be incompletely reduced by denitrifying bacteria, this process is called partial denitrification (PD), which fixes the final reduction product at NO2-N, saving about 40% of the carbon source compared with complete denitrification, and partial denitrification of nitrate is easier to control than partial nitrification [24,31].For mature landfill leachate, a very low BOD content wastewater and PD coupling to the PN/A process can be considered, which can further remove the byproduct nitrate nitrogen and also enhance the long-term operational stability of the system [32,33].
Under the concentration of influent ammonia and nitrate of 47.5 mg/L and 93.7 mg/L in a SBR after PN/A process, a TN removal efficiency of 84.8% was obtained with the effluent TN at less than 20 mg/L [34]. In a continuous flow system, which consisted of an upflow sludge blanket (USB-1), a multi-stage aeration and a second USB (USB-2), PD/A can also be achieved successfully. This process greatly improved NH4+-N and TN removal from leachate, reaching a 95% efficiency [28]. The carbon source for initiating PD has been studied with diluted landfill leachate and domestic sewage, where supplementary carbon sources were used for the denitrification of mature landfill leachate [35,36,37]. The related treatment cost for waste activated sludge (WAS), as a wastewater treatment byproduct, accounts for over 60% of the waste water treatment plant (WWTP) operation cost. Now, more studies focus on sludge fermentation liquid to drive partial denitrification (PD). The residual sludge provides biodegradable carbon, such as proteins, polysaccharides and/or volatile fatty acids, through the anaerobic fermentation process. Thus, researchers have carried out relevant studies to introduce the sludge fermentation IFD process to treating mature landfill leachate. The system remains stable after long term operation and achieved more than a 95% nitrogen removal rate [38].
Figure 1. Nitrogen removal pathway of anammox based processes.
Figure 1. Nitrogen removal pathway of anammox based processes.
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Table 1. Anammox based processes of treating mature landfill leachate.
Table 1. Anammox based processes of treating mature landfill leachate.
ProcessReactorT (°C)C/NInfluent
(mg/L)
Effluent (mg/L)NRE (%)NRR
kgN/(m3 d)
Ref
PN/ASBR301.37NH4+ = 950 ± 20 TN = 1200TN = 37.696.10.397[23]
PN/AUSB-1.2NH4+ = 900 ± 100 COD = 1300 ± 50TN < 6096.3-[22]
PN/ASBR UASB25–331.75NH4+ = 1040 ± 300 TN = 1050 ± 350 COD = 1800 ± 200TN < 5085.10.75 ± 0.12[18]
PN/ASBBR25–300.7NH4+ = 3000 ± 100 COD = 3000 ± 100TN < 20950.51[20]
SNADSBBR 0.5NH4+ = 2004 ± 14.7 TN = 2024 ± 23.6 COD = 1026.8 ± 14.2TN < 12094.9 [27]
SPNADSBR 0.85NH4+ = 1000 ± 250 TN = 1300 ± 75 COD = 1100 ± 200TN = 3798.70.23[30]
DN-PN/AUASB 1NH4+ = 2500 ± 250 COD = 2500 ± 250TN < 90960.5[26]
PN/A-PD/AA/O UASB -NH4+ = 1500 ± 150 TN = 1400 ± 400 COD = 2300 ± 150TN = 15.798.8 [34]
PN/A-PD/ASBR NH4+ = 804.9 COD = 1116TN = 19.287.9 [32]
PN/A-PD/AUASB A/O30–352–3NH4+ = 415 ± 15 TN = 430 ± 10TN = 2092 [35]

3. Microbiological Analysis of Stable Nitrogen Removal Performance

In the mature landfill leachate treatment using anammox based processes, the enrichment of functional microorganisms is a key factor to determine nitrogen remove efficiency. Candidatus Brocadi, Candidatus Jettenia and Candidatus Kuenenia are the most important genera of anammox bacteria. Different process types have certain selection effects on functional microorganisms, and each has its functional bacteria, which are determined by the different control strategies and the function of the reactor itself. In the two stage PN/A processes, each reactor needs different regulation methods. For example, in the PN section, AOB should be enriched and the growth of NOB should be avoided, and the effluent quality can meet the requirements of the substrate proportion for the next part of the anammox reactor [39]. Microorganisms, in one stage processes, are more complex and diverse because all kinds of biochemical reactions are taking place in a single reactor. To achieve the ideal nitrogen removal rate, more precise strategies are required, such as the time regulation of the intermittent aeration mode [40].
Intermittent aeration and endpoint pH control techniques are widely used in the anammox based processes to treat mature landfill leachate and have been proven to be effective control methods [18,31,41]. In the PN/A process, the aeration mode was changed from continuous to intermittent, and the corresponding functional microbial gene hzsB increased from 1.5 × 107 to 1.1 × 108 copies/g, and anammox activity was enhanced significantly [17]. Through the real time control strategy of pH, the time interval of aeration/anoxia in the Simultaneous nitrification, anammox and denitrification (SNAD) process has been precisely controlled. AnAOB and AOB increased by 40.6% and two times, as compared to the initial start up stage [42].
Mature landfill leachate contains refractory organic matter and toxic substances. Due to long term exposure to mature landfill leachate, the breeding of some special bacteria play an important role in maintaining the stability of the process operation. For example, Nitrosomonas eutropha and Nitrosomonas communis are AOB bacteria, but they grow to be heterotrophic in landfill leachate, having a certain degradation characteristic of the aromatic compounds, indicating that the functional bacteria will gradually adapt to such unfavorable conditions [29]. In the SNAD or PD process, specific denitrifying bacteria, such as Azoarcus tolulyticus and Ferruginibacter alkalilentus, have been reported for the biodegradation of toxic substances. Acidobacteria, a special denitrifying bacterial, not only can degrade HA but can also produce a copious amount of EPS; this contributed to the stability of the PN/A system [43].

4. Challenges in Anammox Based Processes for Treating Mature Landfill Leachate

Although the sidestream anammox process has been applied in engineering, more than 100 high ammonia wastewater treatment plants have been established [12]. There are also several challenges that need to be solved. The unstable influent conditions would cause the difficulty of operation. In addition, the maintenance of the activity of major functional bacteria is also facing challenges under seasonal temperature variation.

4.1. Unstable Influent Condition

4.1.1. The Salinity and Heavy Metal

Mature landfill leachate is one kind of high salinity wastewater. When it is treated by biochemical methods, the impact of salinity on bacteria must be considered. Excessive salinity will lead to the disintegration of functional bacterial cells, loss of activity, and dehydration death [44]. A series of batch tests have been conducted to examine the short- term effects of different salinity on anammox bacterial activity, a significant decrease in the removal efficiency of total nitrogen was observed in the presence of over 5 g/L salinity [45,46,47]. In addition, salinity inhibits the activity of AOB. Nitrosomonas, the modal AOB of PN/A, was greatly suppressed at a salinity of >1.65% [48]. Interestingly, heterotrophic bacteria became dominant in the anammox based process with an increase in salt concentration, which could be a cause of anammox system failure [49]. These results showed that high salinity negatively affects the anammox based process stability when treating mature landfill leachate. AnAOB has a different tolerance to salinity, which can be domesticated in a saline environment [50,51]. A PN/A process was applied to treat NaCl amended landfill leachate. The reactor established robust nitrogen removal of 85.7 ± 2.4% with incremental salinity from 0.61% to 3.10% [52]. However, its activity would be inhibited when salinity beyond a certain range. When salinity increased from 10 to 35 g/L, the removal efficiency of one UASB-A/O decreased the biological nitrogen removal system from 99.3 to 83.9% [50]. The major difficulty is sustaining satisfactory anammox activity at high salinity. The effective utilization of marine anammox bacteria (MAB) will notably accelerate the anammox based process to treat saline wastewater [53]. However, another study thought the application of salt acclimated freshwater anammox bacteria could be a more suitable way to treat such wastewaters, MAB based PN/As can be disturbed and even deteriorated while saline wastewater was temporarily not available due to special situations because of MAB’s high dependence on salinity [54]. After a period of acclimation, anammox bacteria can adapt to salinity shock and keep the nitrogen removal rate stable, but too high a salinity shock (>50 g/L) will inhibit the activity of anammox bacteria and make it difficult for the system to restore stability [55].
In addition to salinity, mature landfill leachate also contains a certain amount of heavy metals.
A high concentration of metals is commonly toxic to microorganisms because metals cannot be degraded and thus accumulate in cells [56]. Many studies have researched the inhibit effect of toxic metals in some types of wastewater, such as landfill leachate. The content of heavy metals in landfill leachate is inversely proportional to age. However, its toxic effects cannot be ignored. In the presence of both salinity and heavy metals, its inhibitory effect is stronger than that of salinity or heavy metals alone. In addition, one study points out the joint inhibitory effect of Cu (II) and Zn (II), which initially tended to increase and then reversed as the concentrations increased [57].
In a word, anammox bacterial can be adapted to a certain range of salinity and heavy metals after a period of accumulation [58]. However, it is recommended to remove them in advance to avoid the adverse impact on AnAOB activity in high salinity and heavy metals.

4.1.2. Organic Matter

Mature landfill leachate consists of organic matter, which can inhibit the activity of bacterial [59]. This part of the organic matter can be divided into two categories, one is obviously toxic to bacteria, such as phenol and antibiotics [60,61,62]. The other is biochemical organic matter. These toxic substances can destroy the integrity of cells due to damaged biofilm components [63]. The semi-inhibitory concentrations of phenol and oxytetracycline to anammox acute toxicity are 861.7 and 682.6 mg/L, respectively [64]. The concentration of toxic substances in mature landfill leachate tends to be lower than the lowest tolerance level [65]. However, the joint toxicity between toxic components in landfill leachate should be noted [66]. Moreover, the quantity of leachate is highly variable [67], which may result in a substrate shortage, which could markedly improve the inhibition of toxic organics on anammox activity [68].
The other is biochemical organic matter. Too high an organic carbon content will inhibit the activity of AnAOB. The main inhibition mechanism is that the growth rate of heterotrophic denitrifying bacteria is faster than that of anammox bacteria. It cannot compete with heterotrophic denitrifying bacteria for nitrite. The anammox process will gradually evolve into a heterotrophic denitrification process under high organic concentrations [69,70], as shown in Figure 2. The COD of mature landfill leachate is mainly refractory [19], and the BOD5/COD ratio is even lower than 0.1. The growth of heterotrophic bacteria is limited by the content of organic matter, and denitrification will not dominate under BOD deficit conditions [67]. In fact, the BOD content is too low to provide sufficient electron donor for denitrification or even partial denitrification, so as to further limit the nitrogen removal efficiency [69]. Humic acid accounted for 60% of organic carbon in mature landfill leachate. It is a non-biodegradable organic matter [70]. The traditional view holds that humic acid inhibited the anammox activity and decreased the nitrogen removal efficiency. One study found that nitrogen removal performance was decreased due to humic acid inhibition on AnAOB, but it was relieved after adaptation [28]. However, when salinity and humic acid coexisted in an anammox reactor, a synergistic inhibition would occur, which was far greater than that of the single salinity or humic acid [71].

4.1.3. High Strength Nitrogen

The ammonia nitrogen concentration of mature landfill leachate is usually higher than 2000 mg/L. However, if the concentration is too high, it will inhibit the activity of anammox bacteria. The real inhibition is not the ammonia nitrogen itself, but the free ammonia (FA) produced by it. FA inhibits specific enzymes and destroys EPS, resulting in cell inactivation/lysis [72]. It is generally believed that FA can inhibit the activity of AnAOB by 50% and 80% at 38 mg/L and 100 mg/L, respectively. High concentrations of free nitrite acid (FNA), could also be generated in the anammox based system when treating mature landfill leachate. AnAOB was more sensitive to the inhibition of free nitrite acid due to the biological toxicity of NO2-N. Free nitrite acid showed inhibition to different anammox systems and AnAOB sludge. Most results suggest that when the solubility of nitrite nitrogen is higher than 320 mg/L, its possible inhibitory effect should be considered [72,73]. In addition, the inhibitory effect of FA on AOB cannot be ignored in the SNAD or PD processes. Just 25 mg/L FA could reduce the activity of AOB by 40% [74]. FA concentration in the solution is related with the NH4+-N concentration, pH, and temperature. The pH of mature landfill leachate is often higher than 7.5, and the physiological pH of anammox bacteria is 6.7–8.3 [9]. At leachate pH values >8.0, the FA level rises rapidly.
Fortunately, the inhibition is reversible, and the free ammonia does not change the physical properties of anammox bacteria continuously. The influence of FA and FNA on anammox reactions cannot be predicted and can only be determined through experiments. In order to ensure the efficient and stable operation of anammox systems, substrate concentration should be controlled at the predetermined threshold [75].

4.2. Difficulty in Operational Control

The cooperation and competition among functional microorganisms are crucial to the stability and performance of the anammox process, such as the active coordination between AOB and AnAOB, NOB inhibition, and HB growth control. In addition to influent conditions, the long-term operation stability is also closely related to the operational conditions. The main difficulty is how to maintain advanced nitrogen removal during long term operation [32]. The endpoint of pH, as a process control method with pH as an indicator, is a widely adopted regulation strategy in treating landfill leachate. Indeed, pH usually serves as a real time control parameter for nitritation because there is significant variation in the pH profile during the nitrification process. It has been shown that the use of the endpoint pH control technique in an SBR treating landfill leachate is feasible to achieve a stable PN performance [76]. The inflection point on the pH curve is used to determine whether the nitrification or anammox reaction is complete. The lowest point in the pH profile is known as the “ammonia valley”. This “ammonia valley” indicates the termination of nitritation, preventing nitrite from being oxidized into nitrate [9].

4.2.1. The Control of DO

DO is a very important regulation parameter. The cooperation and competition among functional microorganisms are closely related to DO in the reactor. For example, too much dissolved oxygen can lead to the overgrowth of NOB. NOB growth tends to be a major challenge faced by the PN/A process. Studies have found that AOB has a higher affinity for oxygen than NOB, which means that a low DO concentration could inhibit NOB growth and activity [77]. In the one step PN/A process, when DO increases from 0.2 to 0.6 mg/L, the denitrification efficiency becomes worse. When DO = 0.6 mg/L, AnAOB activity was inhibited, leading to the accumulation of NO2-N in the effluent. The system has a better nitrogen removal rate at a lower DO concentration (<0.6 mg/L) [24]. Four identical sequencing biofilm batch reactors (SBBR) were used to evaluate the effects of dissolved oxygen (DO) on the performance and microbial community of a single stage PN/A system when treating mature landfill leachate. The result showed that an average total nitrogen removal efficiency (TNRE) above 90% was achieved with an optimal DO concentration of 2.7 mg/L [78]. A PNABR process treated mature landfill leachate: when DO rose to 4 mg/L in the aeration stage, the maximum NRE of the system could also reach 96.1% [34]. In the SNAD and the PN reactor, the control of DO is also different: the low DO is less than 0.5 mg/L, and the high is more than 2 mg/L [79].

4.2.2. The Control of C/N

PD can be combined with anammox to realize further nitrogen removal from landfill leachate. when challenged with an overloaded DO concentration and the failure of the real time control of pH. The PN/A-PD/A was proven to be a robust and stable alternative process [32]. However, there exists a difficulty in the accurate control of operational parameters for partial denitrification [80]. In the anammox process, coupled with partial denitrification, a collaboration between heterotrophic bacteria is crucial. Excessive proliferation of heterotrophic bacteria will compete with anammox bacteria for the substrate. The growth of denitrifying microorganisms needs to be strictly controlled. Hence, the optimal C/N ratio is a key control factor for an effective partial denitrification and anammox process. However, regarding the optimal C/N ratio, different studies have different results. This is likely due to the difference in the organic matter of influent, operating conditions, anammox bacterial activity, and the type of reactors [31].

4.3. The Seasonal Temperature Variation

The optimal temperature for an anammox based process is ranged from 30 °C to 40 °C [81]. The lower temperature range (15–25 °C) creates a bottleneck problem, meaning that the anammox process is difficult to achieve in municipal wastewater treatment. In the side stream anammox system, the treatment of landfill leachate also faces the same problem. The side stream anammox system requires a higher temperature, which usually has high activity and a nitrogen removal rate above 30 °C [82]. However, the seasonal temperature of landfill leachate varies greatly. Under the condition of low temperatures (<20 °C), the activity and growth of AnAOB bacteria and AOB will both be affected [83,84]. The temperature can also change the content of free ammonia and organic matter, which indirectly affects the activity of microorganisms [85].
Regardless of a one stage or multistage anammox process of mature landfill leachate, the nitrogen removal rate of the whole process will decrease, to a certain extent, as the temperature drops. In addition, the stability of the system is easily affected by the fluctuation in influent at low temperatures [25,86]. With the seasonal temperature decreasing from 34 °C to 11.3 °C, the total nitrogen removal rate of DN–PN–anammox system treating mature landfill leachate decreased from 1.42 kg N/ (m3·d) to 0.49 kg N/ (m3·d). The fluctuation in NH4+-N concentration in influent has a great influence on process stability, and the effluent easily deteriorates at low temperatures (<20 °C) [87]. Moreover, the influence of the toxic substances (heavy metals and organic substances) in landfill leachate on microbial community structure and functional microbial species might increase at low temperatures (See in Table 2) [88].
The quality of mature landfill leachate is complex and changeable. In a low temperature environment, more attention should be paid to these inhibiting factors, which puts forward higher requirements on the control methods. Both increasing effluent sludge reflux and prolonging hydraulic retention time have been proven to be effective control methods. When the temperature drops from 20–22 °C to 13–15 °C, the contribution of anammox to ammonia nitrogen removal drops from 29.3% to 11.4%. Through the regulation measures of effluent reflux and sludge reflux, the inhibitory effect of organic matter on AnAOB in a low temperature environment can be effectively reduced [86]. In addition, the acclimation and enrichment of sludge under low temperature conditions are also very important. Conducting a low-temperature acclimation process for the sludge under the condition of artificial water distribution, and then gradually introduce landfill leachate as influent after adaptation, so that the system can also achieve stability, has also been studied [25].

5. Future Perspective

Although an anammox process has the merit of saving the carbon source and aeration energy in the treatment of mature landfill leachate, its practical application still faces several challenges. With the increasingly stringent national emission standards and the emphasis on carbon neutralization and resource conservation. Recommended areas for future research are as follows:
More novel nitrogen removal microorganisms can be found and applied to treat mature landfill leachate. The coupled systems can improve the removal efficiency and reduce the treatment cost. These microorganisms can make use of ions in mature landfill leachate as an electron acceptor. Some researchers have verified the feasibility of these coupling processes [106,107,108,109,110]. S-anammox coupled with anammox technology has been successfully applied to treat landfill leachate in some cases, but most of them are applied in multistage [107]. The one stage coupling process needs to be further studied in terms of operation stability, control parameters, and micro microbial mechanism. Rather, most feammox only focus on the mechanism under the condition of artificial water distribution [109], and there are few reports on the treatment of actual landfill leachate.
Given the low BOD content of mature landfill leachate and the additional operating cost of external carbon sources, it is necessary to identify some cheap and easily available new carbon sources and study their applicability. For example, municipal solid waste will produce a certain amount of methane in the landfill process, and some of them will exist in the landfill leachate in the form of dissolved gas [111,112]. However, this methane is not fully utilized and is mostly discharged into the atmosphere in the form of waste. The greenhouse effect caused by methane is 28 times that of carbon dioxide. The discovery of nitrate/nitrite dependent anaerobic methane oxidation processes provides an opportunity to use methane and improve the denitrification performance of anammox based processes. However, the DAMO–anammox system has been only tested on lab scale. Therefore, further studies aimed at assessing the effects of leachate composition, such as organic matter, heavy metals, salinity, and suspended solids, should be conducted [113,114]. In addition to methane, waste fruits can also be used as an external carbon source. Four kinds of rotten fruits were utilized as new carbon sources to promote nitrogen removal from mature landfill leachate. Moreover, this carbon source is cheap and has no inhibitory effect on functional bacteria [115].

6. Conclusions

The main progress of this review is the comprehensive analysis of anammox based processes treating mature landfill leachate based on the state of the art anammox processes for mature landfill leachate. It was demonstrated that anammox based processes are suitable for the removal of nitrogen from mature landfill leachate. No matter what process type, it can achieve the desired nitrogen removal rate on the premise of proper operation. At the same time, microbiological analysis of stable nitrogen removal performance was given, and some special species in the mature landfill leachate treatment were also described. The engineering applications also face several challenges: unstable influent condition, operational control and seasonal temperature variation. Ultimately, novel nitrogen removal coupled systems and the creation of new carbon sources as perspectives with the aim of improving the application of anammox based processes were proposed. Consequently, the value of anammox based processes for nitrogen removal from mature landfill leachate is a significant area worthy of further research.

Author Contributions

Conceptualization and formal analysis, D.G.; investigation, writing—original draft preparation, W.D., L.W., L.C. and W.Y.; writing—review and editing, W.D. and L.W.; visualization, W.D.; supervision, D.G. All authors have read and agreed to the published version of the manuscript.

Funding

This research project was commissioned and funded by Shanghai SUS REMEDIATION Co., LTD (J2021023).

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Kjeldsen, P.; Barlaz, M.A.; Rooker, A.P.; Baun, A.; Ledin, A.; Christensen, T.H. Present and long-term composition of MSW landfill leachate: A review. Crit. Rev. Environ. Sci. Technol. 2002, 32, 297–336. [Google Scholar] [CrossRef]
  2. Luo, H.; Zeng, Y.; Cheng, Y.; He, D.; Pan, X. Recent advances in municipal landfill leachate: A review focusing on its characteristics, treatment, and toxicity assessment. Sci. Total Environ. 2020, 703, 135468. [Google Scholar] [CrossRef]
  3. Mohammad-pajooh, E.; Weichgrebe, D.; Cuff, G. Municipal landfill leachate characteristics and feasibility of retrofitting existing treatment systems with deammonification—A full scale survey. J. Environ. Manag. 2017, 187, 354–364. [Google Scholar] [CrossRef] [PubMed]
  4. Costa, A.M.; Alfaia, R.G.D.S.M.; Campos, J.C. Landfill leachate treatment in Brazil—An overview. J. Environ. Manag. 2019, 232, 110–116. [Google Scholar] [CrossRef] [PubMed]
  5. Cortez, S.; Teixeira, P.; Oliveira, R.; Mota, M. Evaluation of Fenton and ozone-based advanced oxidation processes as mature landfill leachate pre-treatments. J. Environ. Manag. 2011, 92, 749–755. [Google Scholar] [CrossRef] [Green Version]
  6. Chemlal, R.; Azzouz, L.; Kernani, R.; Abdi, N.; Lounici, H.; Grib, H.; Drouiche, N. Combination of advanced oxidation and biological processes for the landfill leachate treatment. Ecol. Eng. 2014, 73, 281–289. [Google Scholar] [CrossRef]
  7. Di Iaconi, C.; Ramadori, R.; Lopez, A. Combined biological and chemical degradation for treating a mature municipal landfill leachate. Biochem. Eng. J. 2006, 31, 118–124. [Google Scholar] [CrossRef]
  8. Canziani, R.; Emondi, V.; Garavaglia, M.; Malpei, F.; Pasinetti, E.; Buttiglieri, G. Effect of oxygen concentration on biological nitrification and microbial kinetics in a cross-flow membrane bioreactor (MBR) and moving-bed biofilm reactor (MBBR) treating old landfill leachate. J. Membr. Sci. 2006, 286, 202–212. [Google Scholar] [CrossRef]
  9. Miao, L.; Yang, G.; Tao, T.; Peng, Y. Recent advances in nitrogen removal from landfill leachate using biological treatments—A review. J. Environ. Manag. 2019, 235, 178–185. [Google Scholar] [CrossRef]
  10. Zhu, R.; Wang, S.; Li, J.; Wang, K.; Miao, L.; Ma, B.; Peng, Y. Biological nitrogen removal from landfill leachate using anaerobic-aerobic process: Denitritation via organics in raw leachate and intracellular storage polymers of microorganisms. Bioresour. Technol. 2013, 128, 401–408. [Google Scholar] [CrossRef] [PubMed]
  11. Liang, Y.C.; Daverey, A.; Huang, Y.T.; Sung, S.; Lin, J.G. Treatment of semiconductor wastewater using single-stage partial nitrification and anammox in a pilot-scale reactor. J. Taiwan Inst. Chem. Eng. 2016, 63, 236–242. [Google Scholar] [CrossRef]
  12. Lackner, S.; Gilbert, E.M.; Vlaeminck, S.E.; Joss, A.; Horn, H.; van Loosdrecht, M.C.M. Full-scale partial nitritation/anammox experiences—An application survey. Water Res. 2014, 55, 292–303. [Google Scholar] [CrossRef]
  13. Chen, H.; Hu, H.Y.; Chen, Q.Q.; Shi, M.L.; Jin, R.C. Successful start-up of the anammox process: Influence of the seeding strategy on performance and granule properties. Bioresour. Technol. 2016, 211, 594–602. [Google Scholar] [CrossRef] [PubMed]
  14. Qin, Y.J.; Han, B.; Cao, Y.; Wang, T.Y. Impact of substrate concentration on anammox-UBF reactors start-up. Bioresour. Technol. 2017, 239, 422–429. [Google Scholar] [CrossRef]
  15. Tang, C.J.; Zheng, P.; Chai, L.Y.; Min, X.B. Thermodynamic and kinetic investigation of anaerobic bioprocesses on ANAMMOX under high organic conditions. Chem. Eng. J. 2013, 230, 149–157. [Google Scholar] [CrossRef]
  16. Jetten, M.S.M.; Niftrik, L.V.; Strous, M.; Kartal, B.; Keltjens, J.T.; Op Den Camp, H.J.M. Biochemistry and molecular biology of anammox bacteria biochemistry and molecular biology of anammox bacteria. Crit. Rev. Biochem. Mol. Biol. 2009, 44, 65–84. [Google Scholar] [CrossRef] [PubMed]
  17. Chen, Y.; Zhao, Z.; Liu, H.; Ma, Y.; An, F.; Huang, J.; Shao, Z. Achieving stable two-stage mainstream partial-nitrification/anammox (PN/A) operation via intermittent aeration. Chemosphere 2020, 245, 125650. [Google Scholar] [CrossRef]
  18. Li, H.; Zhou, S.; Ma, W.; Huang, P.; Huang, G.; Qin, Y.; Xu, B.; Ouyang, H. Long-term performance and microbial ecology of a two-stage PN-ANAMMOX process treating mature landfill leachate. Bioresour. Technol. 2014, 159, 404–411. [Google Scholar] [CrossRef]
  19. Wang, Z.; Peng, Y.; Miao, L.; Cao, T.; Zhang, F.; Wang, S.; Han, J. Continuous-flow combined process of nitritation and ANAMMOX for treatment of landfill leachate. Bioresour. Technol. 2016, 214, 514–519. [Google Scholar] [CrossRef]
  20. Miao, L.; Wang, S.; Cao, T.; Peng, Y.; Zhang, M.; Liu, Z. Advanced nitrogen removal from landfill leachate via Anammox system based on Sequencing Biofilm Batch Reactor (SBBR): Effective protection of biofilm. Bioresour. Technol. 2016, 220, 8–16. [Google Scholar] [CrossRef]
  21. Li, J.; Li, J.; Peng, Y.; Wang, S.; Zhang, L.; Yang, S.; Li, S. Insight into the impacts of organics on anammox and their potential linking to system performance of sewage partial nitrification-anammox (PN/A): A critical review. Bioresour. Technol. 2020, 300, 122655. [Google Scholar] [CrossRef]
  22. Antwi, P.; Zhang, D.; Su, H.; Luo, W.; Quashie, F.K.; Kabutey, F.T.; Xiao, L.; Lai, C.; Liu, Z.; Li, J. Nitrogen removal from landfill leachate by single-stage anammox and partial-nitritation process: Effects of microaerobic condition on performance and microbial activities. J. Water Process Eng. 2020, 38, 101572. [Google Scholar] [CrossRef]
  23. Jiang, H.; Peng, Y.; Li, X.; Zhang, F.; Wang, Z.; Ren, S. Advanced nitrogen removal from mature landfill leachate via partial nitrification-Anammox biofilm reactor (PNABR) driven by high dissolved oxygen (DO): Protection mechanism of aerobic biofilm. Bioresour. Technol. 2020, 306, 123119. [Google Scholar] [CrossRef] [PubMed]
  24. Cao, S.; Du, R.; Zhou, Y. Coupling anammox with heterotrophic denitrification for enhanced nitrogen removal: A review. Crit. Rev. Environ. Sci. Technol. 2021, 51, 2260–2293. [Google Scholar] [CrossRef]
  25. Wang, Y.; Gong, B.; Lin, Z.; Wang, J.; Zhang, J.; Zhou, J. Robustness and microbial consortia succession of simultaneous partial nitrification, ANAMMOX and denitrification (SNAD) process for mature landfill leachate treatment under low temperature. Biochem. Eng. J. 2018, 132, 112–121. [Google Scholar] [CrossRef]
  26. Li, X.; Lu, M.Y.; Qiu, Q.C.; Huang, Y.; Li, B.L.; Yuan, Y.; Yuan, Y. The effect of different denitrification and partial nitrification-Anammox coupling forms on nitrogen removal from mature landfill leachate at the pilot-scale. Bioresour. Technol. 2020, 297, 122430. [Google Scholar] [CrossRef] [PubMed]
  27. Wang, Y.; Lin, Z.; He, L.; Huang, W.; Zhou, J.; He, Q. Simultaneous partial nitrification, anammox and denitrification (SNAD) process for nitrogen and refractory organic compounds removal from mature landfill leachate: Performance and metagenome-based microbial ecology. Bioresour. Technol. 2019, 294, 122166. [Google Scholar] [CrossRef]
  28. Luo, X.; Shen, L.; Meng, F. Response of microbial community structures and functions of nitrosifying consortia to biorefractory humic substances. ACS Sustain. Chem. Eng. 2019, 7, 4744–4754. [Google Scholar] [CrossRef]
  29. Liu, L.; Ji, M.; Wang, F.; Wang, S.; Qin, G. Insight into the influence of microbial aggregate types on nitrogen removal performance and microbial community in the anammox process—A review and meta-analysis. Sci. Total Environ. 2020, 714, 136571. [Google Scholar] [CrossRef]
  30. Zhang, F.; Peng, Y.; Wang, S.; Wang, Z.; Jiang, H. Efficient step-feed partial nitrification, simultaneous Anammox and denitrification (SPNAD) equipped with real-time control parameters treating raw mature landfill leachate. J. Hazard. Mater. 2019, 364, 163–172. [Google Scholar] [CrossRef]
  31. Du, R.; Peng, Y.; Ji, J.; Shi, L.; Gao, R.; Li, X. Partial denitrification providing nitrite: Opportunities of extending application for anammox. Environ. Int. 2019, 131, 105001. [Google Scholar] [CrossRef]
  32. Zhang, F.; Peng, Y.; Liu, Y.; Zhao, L. Improving stability of mainstream Anammox in an innovative two-stage process for advanced nitrogen removal from mature landfill leachate. Bioresour. Technol. 2021, 340, 125617. [Google Scholar] [CrossRef]
  33. Wu, L.; Li, Z.; Zhao, C.; Liang, D.; Peng, Y. A novel partial-denitrification strategy for post-anammox to effectively remove nitrogen from landfill leachate. Sci. Total Environ. 2018, 633, 745–751. [Google Scholar] [CrossRef]
  34. Wu, L.; Zhang, L.; Shi, X.; Liu, T.; Peng, Y.; Zhang, J. Analysis of the impact of reflux ratio on coupled partial nitrification-anammox for co-treatment of mature landfill leachate and domestic wastewater. Bioresour. Technol. 2015, 198, 207–214. [Google Scholar] [CrossRef]
  35. Wu, L.; Li, Z.; Huang, S.; Shen, M.; Yan, Z.; Li, J.; Peng, Y. Low energy treatment of landfill leachate using simultaneous partial nitrification and partial denitrification with anaerobic ammonia oxidation. Environ. Int. 2019, 127, 452–461. [Google Scholar] [CrossRef]
  36. Zhang, F.; Li, X.; Wang, Z.; Jiang, H.; Ren, S.; Peng, Y. Simultaneous Ammonium oxidation denitrifying (SAD) in an innovative three-stage process for energy-efficient mature landfill leachate treatment with external sludge reduction. Water Res. 2020, 169, 121615. [Google Scholar] [CrossRef]
  37. Zhang, F.; Peng, Y.; Wang, Z.; Jiang, H.; Ren, S.; Qiu, J. New insights into co-treatment of mature landfill leachate with municipal sewage via integrated partial nitrification, Anammox and denitratation. J. Hazard. Mater. 2021, 415, 125506. [Google Scholar] [CrossRef]
  38. Zhang, F.; Peng, Y.; Wang, Z.; Jiang, H. High-efficient nitrogen removal from mature landfill leachate and waste activated sludge (WAS)reduction via partial nitrification and integrated fermentation-denitritation process (PNIFD). Water Res. 2019, 160, 394–404. [Google Scholar] [CrossRef]
  39. Strous, M.; Van Gerven, E.; Zheng, P.; Kuenen, J.G.; Jetten, M.S.M. Ammonium removal from concentrated waste streams with the anaerobic ammonium oxidation (anammox) process in different reactor configurations. Water Res. 1997, 31, 1955–1962. [Google Scholar] [CrossRef] [Green Version]
  40. Qiu, S.; Hu, Y.; Liu, R.; Sheng, X.; Chen, L.; Wu, G.; Hu, H.; Zhan, X. Start up of partial nitritation-anammox process using intermittently aerated sequencing batch reactor: Performance and microbial community dynamics. Sci. Total Environ. 2019, 647, 1188–1198. [Google Scholar] [CrossRef]
  41. Nhat, P.T.; Biec, H.N.; Van, T.T.T.; van Tuan, D.; Trung, N.L.H.; Nghi, V.T.K.; Dan, N.P. Stability of partial nitritation in a sequencing batch reactor fed with high ammonium strength old urban landfill leachate. Int. Biodeterior. Biodegrad. 2017, 124, 56–61. [Google Scholar] [CrossRef]
  42. Zhang, F.Z.; Peng, Y.; Miao, L.; Wang, Z.; Wang, S.; Li, B. A novel simultaneous partial nitrification Anammox and denitrification (SNAD) with intermittent aeration for cost-effective nitrogen removal from mature landfill leachate. Chem. Eng. J. 2017, 313, 619–628. [Google Scholar] [CrossRef]
  43. Lu, C.; Yuan, C.; Zhu, T.; Wang, Y. Effect of humic acid on the single-stage nitrogen removal using anammox and partial nitritation (SNAP) process: Performance and bacterial communities. J. Environ. Chem. Eng. 2021, 9, 106680. [Google Scholar] [CrossRef]
  44. Abou-Elela, S.I.; Kamel, M.M.; Fawzy, M.E. Biological treatment of saline wastewater using a salt-tolerant microorganism. Desalination 2010, 250, 1–5. [Google Scholar] [CrossRef]
  45. Ma, C.; Jin, R.C.; Yang, G.F.; Yu, J.J.; Xing, B.S.; Zhang, Q.Q. Impacts of transient salinity shock loads on Anammox process performance. Bioresour. Technol. 2012, 112, 124–130. [Google Scholar] [CrossRef]
  46. Jeong, D.; Kim, W.; Lim, H.; Bae, H. Shift in bacterial community structure in response to salinity in a continuous anaerobic ammonium oxidation (anammox) reactor. Int. Biodeterior. Biodegrad. 2020, 147, 104873. [Google Scholar] [CrossRef]
  47. Van de Vossenberg, J.; Woebken, D.; Maalcke, W.J.; Wessels, H.J.C.T.; Dutilh, B.E.; Kartal, B.; Janssen-Megens, E.M.; Roeselers, G.; Yan, J.; Speth, D.; et al. The metagenome of the marine anammox bacterium “Candidatus Scalindua profunda” illustrates the versatility of this globally important nitrogen cycle bacterium. Environ. Microbiol. 2013, 15, 1275–1289. [Google Scholar] [CrossRef] [Green Version]
  48. Dale, O.R.; Tobias, C.R.; Song, B. Biogeographical distribution of diverse anaerobic ammonium oxidizing (anammox) bacteria in Cape Fear River Estuary. Environ. Microbiol. 2009, 11, 1194–1207. [Google Scholar] [CrossRef]
  49. Huang, X.; Mi, W.; Ito, H.; Kawagoshi, Y. Probing the dynamics of three freshwater Anammox genera at different salinity levels in a partial nitritation and Anammox sequencing batch reactor treating landfill leachate. Bioresour. Technol. 2021, 319, 124112. [Google Scholar] [CrossRef]
  50. Liu, M.; Yang, Q.; Peng, Y.; Liu, T.; Xiao, H.; Wang, S. Treatment performance and N2O emission in the UASB-A/O shortcut biological nitrogen removal system for landfill leachate at different salinity. J. Ind. Eng. Chem. 2015, 32, 63–71. [Google Scholar] [CrossRef]
  51. Meng, Y.; Yin, C.; Zhou, Z.; Meng, F. Increased salinity triggers significant changes in the functional proteins of Anammox bacteria within a biofilm community. Chemosphere 2018, 207, 655–664. [Google Scholar] [CrossRef]
  52. Wang, Y.; Chen, J.; Zhou, S.; Wang, X.; Chen, Y.; Lin, X.; Yan, Y.; Ma, X.; Wu, M.; Han, H. 16S rRNA gene high-throughput sequencing reveals shift in nitrogen conversion related microorganisms in a CANON system in response to salt stress. Chem. Eng. J. 2017, 317. [Google Scholar] [CrossRef]
  53. Li, J.; Qi, P.; Qiang, Z.; Dong, H.; Gao, D.; Wang, D. Is anammox a promising treatment process for nitrogen removal from nitrogen-rich saline wastewater? Bioresour. Technol. 2018, 270, 722–731. [Google Scholar] [CrossRef] [PubMed]
  54. Guo, Y.; Sugano, T.; Song, Y.; Xie, C.; Chen, Y.; Xue, Y.; Li, Y.Y. The performance of freshwater one-stage partial nitritation/anammox process with the increase of salinity up to 3.0%. Bioresour. Technol. 2020, 311, 123489. [Google Scholar] [CrossRef]
  55. Shehzad, A.; Bashir, M.J.K.; Sethupathi, S.; Lim, J.W. An overview of heavily polluted landfill leachate treatment using food waste as an alternative and renewable source of activated carbon. Process Saf. Environ. Prot. 2015, 98, 309–318. [Google Scholar] [CrossRef]
  56. Wu, D.; Li, G.F.; Shi, Z.J.; Zhang, Q.; Huang, B.C.; Fan, N.S.; Jin, R.C. Co-inhibition of salinity and Ni(II) in the anammox-UASB reactor. Sci. Total Environ. 2019, 669, 70–82. [Google Scholar] [CrossRef]
  57. Zhang, Z.Z.; Zhang, Q.Q.; Xu, J.J.; Deng, R.; Ji, Z.Q.; Wu, Y.H.; Jin, R.C. Evaluation of the inhibitory effects of heavy metals on anammox activity: A batch test study. Bioresour. Technol. 2016, 200, 208–216. [Google Scholar] [CrossRef]
  58. Zhou, Y.; Huang, M.; Deng, Q.; Cai, T. Combination and performance of forward osmosis and membrane distillation (FO-MD) for treatment of high salinity landfill leachate. Desalination 2017, 420, 99–105. [Google Scholar] [CrossRef]
  59. Teng, C.; Zhou, K.; Peng, C.; Chen, W. Characterization and treatment of landfill leachate: A review. Water Res. 2021, 203, 117525. [Google Scholar] [CrossRef]
  60. Ramos, C.; Fernández, I.; Suárez-Ojeda, M.E.; Carrera, J. Inhibition of the anammox activity by aromatic compounds. Chem. Eng. J. 2015, 279, 681–688. [Google Scholar] [CrossRef] [Green Version]
  61. Yang, G.F.; Zhang, Q.Q.; Jin, R.C. Changes in the nitrogen removal performance and the properties of granular sludge in an Anammox system under oxytetracycline (OTC) stress. Bioresour. Technol. 2013, 129, 65–71. [Google Scholar] [CrossRef]
  62. Zhang, X.; Chen, T.; Zhang, J.; Zhang, H.; Zheng, S.; Chen, Z.; Ma, Y. Performance of the nitrogen removal, bioactivity and microbial community responded to elevated norfloxacin antibiotic in an Anammox biofilm system. Chemosphere 2018, 210, 1185–1192. [Google Scholar] [CrossRef] [PubMed]
  63. Yang, G.F.; Jin, R.C. The joint inhibitory effects of phenol, copper (II), oxytetracycline (OTC) and sulfide on Anammox activity. Proc. Bioresour. Technol. 2012, 126, 187–192. [Google Scholar] [CrossRef] [PubMed]
  64. Kulikowska, D.; Klimiuk, E. The effect of landfill age on municipal leachate composition. Bioresour. Technol. 2008, 99, 5981–5985. [Google Scholar] [CrossRef]
  65. Hernández, S.M.; Sun, W.; Sierra-Alvarez, R.; Field, J.A. Toluene-nitrite inhibition synergy of anaerobic ammonium oxidizing (anammox) activity. Process Biochem. 2013, 48, 926–930. [Google Scholar] [CrossRef]
  66. Chamchoi, N.; Nitisoravut, S.; Schmidt, J.E. Inactivation of ANAMMOX communities under concurrent operation of anaerobic ammonium oxidation (ANAMMOX) and denitrification. Bioresour. Technol. 2008, 99, 3331–3336. [Google Scholar] [CrossRef]
  67. Lackner, S.; Terada, A.; Smets, B.F. Heterotrophic activity compromises autotrophic nitrogen removal in membrane-aerated biofilms: Results of a modeling study. Water Res. 2008, 42, 1102–1112. [Google Scholar] [CrossRef]
  68. Cassano, D.; Zapata, A.; Brunetti, G.; del Moro, G.; di Iaconi, C.; Oller, I.; Malato, S.; Mascolo, G. Comparison of several combined/integrated biological-AOPs setups for the treatment of municipal landfill leachate: Minimization of operating costs and effluent toxicity. Chem. Eng. J. 2011, 172, 250–257. [Google Scholar] [CrossRef]
  69. Guo, Y.; Zhao, Y.; Zhu, T.; Li, J.; Feng, Y.; Zhao, H.; Liu, S. A metabolomic view of how low nitrogen strength favors anammox biomass yield and nitrogen removal capability. Water Res. 2018, 143, 387–398. [Google Scholar] [CrossRef] [PubMed]
  70. Kang, K.H.; Shin, H.S.; Park, H. Characterization of humic substances present in landfill leachates with different landfill ages and its implications. Water Res. 2002, 36, 4023–4032. [Google Scholar] [CrossRef]
  71. He, C.; Zhang, B.; Ou, H.; Hu, Z.; Wang, W. Inhibitory effect of salinity and humic acid on the performance of anaerobic ammonium oxidation process and recovery of anammox activity. Environ. Eng. Sci. 2021, 38, 11. [Google Scholar] [CrossRef]
  72. Niu, Q.; He, S.; Zhang, Y.; Ma, H.; Liu, Y.; Li, Y.Y. Process stability and the recovery control associated with inhibition factors in a UASB-anammox reactor with a long-term operation. Bioresour. Technol. 2016, 203, 132–141. [Google Scholar] [CrossRef]
  73. He, S.; Zhang, Y.; Niu, Q.; Ma, H.; Li, Y.Y. Operation stability and recovery performance in an Anammox EGSB reactor after pH shock. Ecol. Eng. 2016, 90, 50–56. [Google Scholar] [CrossRef]
  74. Liu, Y.; Ngo, H.H.; Guo, W.; Peng, L.; Wang, D.; Ni, B. The roles of free ammonia (FA) in biological wastewater treatment processes: A review. Environ. Int. 2019, 123, 10–19. [Google Scholar] [CrossRef]
  75. Ye, J.; Liu, J.; Ye, M.; Ma, X.; Li, Y.Y. Towards advanced nitrogen removal and optimal energy recovery from leachate: A critical review of anammox-based processes. Crit. Rev. Environ. Sci. Technol. 2020, 50, 612–653. [Google Scholar] [CrossRef]
  76. Li, H.; Zhou, S.; Huang, G.; Xu, B. Achieving stable partial nitritation using endpoint pH control in an SBR treating landfill leachate. Process Saf. Environ. Prot. 2014, 92, 199–205. [Google Scholar] [CrossRef]
  77. Pichel, A.; Moreno, R.; Figueroa, M.; Campos, J.L.; Mendez, R.; Mosquera-Corral, A.; Val del Rio, A. How to cope with NOB activity and pig manure inhibition in a partial nitritation-anammox process? Sep. Purif. Technol. 2019, 212, 396–404. [Google Scholar] [CrossRef]
  78. Wen, X.; Zhou, J.; Wang, J.; Qing, X.; He, Q. Effects of dissolved oxygen on microbial community of single-stage autotrophic nitrogen removal system treating simulating mature landfill leachate. Bioresour. Technol. 2016, 218, 962–968. [Google Scholar] [CrossRef]
  79. Gabarró, J.; Hernández-del Amo, E.; Gich, F.; Ruscalleda, M.; Balaguer, M.D.; Colprim, J. Nitrous oxide reduction genetic potential from the microbial community of an intermittently aerated partial nitritation SBR treating mature landfill leachate. Water Res. 2013, 47, 7066–7077. [Google Scholar] [CrossRef] [PubMed]
  80. Van Duc, L.; Ito, H.; Hama, T.; Kim, J.; Kawagoshi, Y. A novel reactor combining anammox and Fenton-like reactions for the simultaneous removal of organic carbon and nitrogen at different organic carbon to nitrogen ratios. J. Environ. Manag. 2020, 271, 110832. [Google Scholar] [CrossRef]
  81. Cho, S.; Kambey, C.; Nguyen, V.K. Performance of anammox processes for wastewater treatment: A critical review on effects of operational conditions and environmental stresses. Water. 2020, 12, 20. [Google Scholar] [CrossRef] [Green Version]
  82. Weralupitiya, C.; Wanigatunge, R.; Joseph, S.; Athapattu, B.C.L.; Lee, T.H.; Kumar Biswas, J.; Ginige, M.P.; Shiung Lam, S.; Senthil Kumar, P.; Vithanage, M. Anammox bacteria in treating ammonium rich wastewater: Recent perspective and appraisal. Bioresour. Technol. 2021, 334, 125240. [Google Scholar] [CrossRef] [PubMed]
  83. Lotti, T.; Kleerebezem, R.; van Loosdrecht, M.C.M. Effect of temperature change on anammox activity. Biotechnol. Bioeng. 2015, 112, 98–103. [Google Scholar] [CrossRef] [PubMed]
  84. Dosta, J.; Fernández, I.; Vázquez-Padín, J.R.; Mosquera-Corral, A.; Campos, J.L.; Mata-Álvarez, J.; Méndez, R. Short- and long-term effects of temperature on the Anammox process. J. Hazard. Mater. 2008, 154, 688–693. [Google Scholar] [CrossRef]
  85. Van Hulle, S.W.H.; Volcke, E.I.P.; Teruel, J.L.; Donckels, B.; van Loosdrecht, M.C.M.; Vanrolleghem, P.A. Influence of temperature and pH on the kinetics of the Sharon nitritation process. J. Chem. Technol. Biotechnol. 2007, 82, 471–480. [Google Scholar] [CrossRef]
  86. Wu, L.; Yan, Z.; Huang, S.; Li, J.; Su, B.; Wang, C.; Peng, Y. Rapid start-up and stable maintenance of partial nitrification–anaerobic ammonium oxidation treatment of landfill leachate at low temperatures. Environ. Res. 2020, 191, 110131. [Google Scholar] [CrossRef]
  87. Li, X.; Lu, M.Y.; Huang, Y.; Yuan, Y.; Yuan, Y. Influence of seasonal temperature change on autotrophic nitrogen removal for mature landfill leachate treatment with high-ammonia by partial nitrification-Anammox process. J. Environ. Sci. 2021, 102, 291–300. [Google Scholar] [CrossRef]
  88. Yue, X.; Yu, G.; Liu, Z.; Tang, J.; Liu, J. Fast start-up of the CANON process with a SABF and the effects of pH and temperature on nitrogen removal and microbial activity. Bioresour. Technol. 2018, 254, 157–165. [Google Scholar] [CrossRef]
  89. Tang, C.-J.; Zheng, P.; Wang, C.-H.; Mahmood, Q.; Zhang, J.-Q.; Chen, X.-G.; Zhang, L.; Chen, J.-W. Performance of high-loaded Anammox UASB reactors containing granular sludge. Water Res. 2011, 45, 135–144. [Google Scholar] [CrossRef]
  90. Laureni, M.; Falås, P.; Robin, O.; Wick, A.; Weissbrodt, D.G.; Nielsen, J.L.; Ternes, T.A.; Morgenroth, E.; Joss, A. Mainstream Partial Nitritation and Anammox: Long-Term Process Stability and Effluent Quality at Low Temperatures. Water Res. 2016, 101, 628–639. [Google Scholar] [CrossRef] [Green Version]
  91. García-Ruiz, M.J.; Maza-Márquez, P.; González-López, J.; Osorio, F. Nitrogen removal capacity and bacterial community dynamics of a canon biofilter system at different organic matter concentrations. Chemosphere 2018, 193, 591–601. [Google Scholar] [CrossRef] [PubMed]
  92. Dapena-Mora, A.; Fernández, I.; Campos, J.L.; Mosquera-Corral, A.; Méndez, R.; Jetten, M.S.M. Evaluation of activity and inhibition effects on anammox process by batch tests based on the nitrogen gas production. Enzym. Microb. Technol. 2007, 40, 859–865. [Google Scholar] [CrossRef]
  93. Zhang, Z.-Z.; Zhang, Q.-Q.; Guo, Q.; Chen, Q.-Q.; Jiang, X.-Y.; Jin, R.-C. Anaerobic Ammonium-oxidizing bacteria gain antibiotic resistance during long-term acclimatization. Bioresour. Technol. 2015, 192, 756–764. [Google Scholar] [CrossRef]
  94. Van de Graaf, A.A.; Mulder, A.; de Bruijn, P.; Jetten, M.S.; Robertson, L.A.; Kuenen, J.G. Anaerobic oxidation of Ammonium is a biologically mediated process. Appl. Environ. Microbiol. 1995, 61, 1246–1251. [Google Scholar] [CrossRef] [Green Version]
  95. Fernández, I.; Bravo, J.I.; Mosquera-Corral, A.; Pereira, A.; Campos, J.L.; Méndez, R.; Melo, L.F. Influence of the shear stress and salinity on anammox biofilms formation: Modelling results. Bioprocess. Biosyst. Eng. 2014, 37, 1955–1961. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  96. Windey, K.; de Bo, I.; Verstraete, W. Oxygen-limited autotrophic nitrification–denitrification (OLAND) in a rotating biological contactor treating high-salinity wastewater. Water Res. 2005, 39, 4512–4520. [Google Scholar] [CrossRef]
  97. Lu, H.; Li, Y.; Shan, X.; Abbas, G.; Zeng, Z.; Kang, D.; Wang, Y.; Zheng, P.; Zhang, M. A holistic analysis of Anammox process in response to salinity: From adaptation to collapse. Sep. Purif. Technol. 2019, 215, 342–350. [Google Scholar] [CrossRef]
  98. Jin, R.-C.; Ma, C.; Mahmood, Q.; Yang, G.-F.; Zheng, P. Anammox in a UASB reactor treating saline wastewater. Process Saf. Environ. Prot. 2011, 89, 342–348. [Google Scholar] [CrossRef]
  99. Chen, H.; Ma, C.; Ji, Y.-X.; Ni, W.-M.; Jin, R.-C. Evaluation of the efficacy and regulation measures of the anammox process under salty conditions. Sep. Purif. Technol. 2014, 132, 584–592. [Google Scholar] [CrossRef]
  100. Kartal, B.; Koleva, M.; Arsov, R.; van der Star, W.; Jetten, M.S.M.; Strous, M. Adaptation of a freshwater anammox population to high salinity wastewater. J. Biotechnol. 2006, 126, 546–553. [Google Scholar] [CrossRef]
  101. Yang, G.-F.; Ni, W.-M.; Wu, K.; Wang, H.; Yang, B.-E.; Jia, X.-Y.; Jin, R.-C. The effect of Cu(II) stress on the activity, performance and recovery on the anaerobic ammonium-oxidizing (Anammox) process. Chem. Eng. J. 2013, 226, 39–45. [Google Scholar] [CrossRef]
  102. Guo, Q.; Yang, C.-C.; Xu, J.-L.; Hu, H.-Y.; Huang, M.; Shi, M.-L.; Jin, R.-C. Individual and combined effects of substrate, heavy metal and hydraulic shocks on an anammox system. Sep. Purif. Technol. 2015, 154, 128–136. [Google Scholar] [CrossRef]
  103. Zhang, Q.-Q.; Zhang, Z.-Z.; Guo, Q.; Wang, J.-J.; Wang, H.-Z.; Jin, R.-C. Analyzing the revolution of anaerobic Ammonium oxidation (Anammox) performance and sludge characteristics under zinc inhibition. Appl. Microbiol. Biotechnol. 2015, 99, 3221–3232. [Google Scholar] [CrossRef] [PubMed]
  104. Bi, Z.; Qiao, S.; Zhou, J.; Tang, X.; Cheng, Y. Inhibition and recovery of anammox biomass subjected to short-term exposure of Cd, Ag, Hg and Pb. Chem. Eng. J. 2014, 244, 89–96. [Google Scholar] [CrossRef]
  105. Val del Río, Á.; da Silva, T.; Martins, T.H.; Foresti, E.; Campos, J.L.; Méndez, R.; Mosquera-Corral, A. Partial nitritation-anammox granules: Short-term inhibitory effects of seven metals on Anammox activity. Water Air Soil Pollut. 2017, 228, 439. [Google Scholar] [CrossRef]
  106. Zhou, G.W.; Yang, X.R.; Li, H.; Marshall, C.W.; Zheng, B.X.; Yan, Y.; Su, J.Q.; Zhu, Y.G. Electron shuttles enhance anaerobic ammonium oxidation coupled to iron(III) reduction. Environ. Sci. Technol. 2016, 50, 9298–9307. [Google Scholar] [CrossRef]
  107. Wu, L.; Yan, Z.; Li, J.; Huang, S.; Li, Z.; Shen, M.; Peng, Y. Low temperature advanced nitrogen and sulfate removal from landfill leachate by nitrite-anammox and sulfate-anammox. Environ. Pollut. 2020, 259, 113763. [Google Scholar] [CrossRef]
  108. Madani, R.M.; Liang, J.; Cui, L.; Zhang, D.; Otitoju, T.A.; Elsalahi, R.H.; Song, X. Novel simultaneous anaerobic ammonium and sulfate removal process: A review. Environ. Technol. Innov. 2021, 23, 101661. [Google Scholar] [CrossRef]
  109. Zhu, J.; Li, T.; Liao, C.; Li, N.; Wang, X. A promising destiny for Feammox: From biogeochemical ammonium oxidation to wastewater treatment. Sci. Total Environ. 2021, 790, 148038. [Google Scholar] [CrossRef]
  110. Zeng, C.; Su, Q.; Peng, L.; Sun, L.; Zhao, Q.; Diao, X.; Lu, H. Elemental sulfur-driven autotrophic denitrification for advanced nitrogen removal from mature landfill leachate after PN/A pretreatment. Chem. Eng. J. 2021, 410, 128256. [Google Scholar] [CrossRef]
  111. Feng, S.; Hou, S.; Huang, X.; Fang, Z.; Tong, Y.; Yang, H. Insights into the microbial community structure of anaerobic digestion of municipal solid waste landfill leachate for methane production by adaptive thermophilic granular sludge. Electron. J. Biotechnol. 2019, 39, 98–106. [Google Scholar] [CrossRef]
  112. Warmadewanthi, I.D.A.A.; Chrystiadini, G.; Kurniawan, S.B.; Abdullah, S.R.S. Impact of degraded solid waste utilization as a daily cover for landfill on the formation of methane and leachate. Bioresour. Technol. Rep. 2021, 15, 100797. [Google Scholar] [CrossRef]
  113. Harb, R.; Laçin, D.; Subaşı, I.; Erguder, T.H. Denitrifying anaerobic methane oxidation (DAMO) cultures: Factors affecting their enrichment, performance and integration with anammox bacteria. J. Environ. Manag. 2021, 295, 113070. [Google Scholar] [CrossRef]
  114. Fu, L.; Ding, J.; Lu, Y.Z.; Ding, Z.W.; Zeng, R.J. Nitrogen source effects on the denitrifying anaerobic methane oxidation culture and anaerobic ammonium oxidation bacteria enrichment process. Appl. Microbiol. Biotechnol. 2017, 101, 3895–3906. [Google Scholar] [CrossRef] [PubMed]
  115. Zhu, Z.; Zhao, Y.; Guo, Y.; Zhang, R.; Pan, Y.; Zhou, T. A novel additional carbon source derived from rotten fruits: Application for the denitrification from mature landfill leachate and evaluation the economic benefits. Bioresour. Technol. 2021, 334. [Google Scholar] [CrossRef] [PubMed]
Figure 2. The high concentration organic matter inhibits the anammox process.
Figure 2. The high concentration organic matter inhibits the anammox process.
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Table 2. Effect of organic matter, salinity and heavy metals on the performance of anammox systems.
Table 2. Effect of organic matter, salinity and heavy metals on the performance of anammox systems.
InhibitorTypesReactorConcentrationEffectReference
Organic matterNontoxicUASB700 mg L−1 SucroseNitrogen removal efficiency decreased by 98%[89]
MBBR533 mg L−1 CODNo interruption because nitrogen load was less[90]
Biofilter400 mg L−1 AcetatePartial inhibition of nitrogen removal rate and increase in the heterotrophic bacteria[91]
Serum vials50 mmol L−1 AcetateNitrogen removal efficiency decreased by 70%[92]
ToxicUASB50 mg L−1
Oxytetracycline
Activity loss of 90.4%[61]
150 mg L−1
Amoxicillin
Severely inhibited[93]
Serum vials20 mg L−1
Chloramophenicol
Activity decreased by 36%[94]
200 mg L−1
Chloramophenicol
Activity decreased by 98%
100 mg L−1
Penicillin
Activity decreased by 36%
SalinityNaClSBR5 g L−1Favored the formation of anammox biofilm[95]
15 g L−1Obversed inhibitory effect
RBC6 g L−1No remarkable loss of activity[96]
30 g L−1Activity decreased by 95% (nonadapted) and 59% (adapted)
UASB35.1 g L−1Anammox performance collapsed[97]
30 g L−1Activity decreased by 67.5% (nonadapted) and 45.1% (adapted)[98]
5–30 g L−1Performance degraded at NaCl higher than 15 g/L[99]
90% NaCl and 10% KClSBR10 g L−1Maximum activity[100]
45 g L−1Decreased by 85%
60 g L−1The activity was lost
Na2SO4Serum vials11.36 g L−1Inhibition by 50%[92]
CaCl2SBR5 g L−1Favored the formation of anammox biofilm[95]
Heavy metalCuSerum flask12.6 mg L−1Inhibition by 50%[101]
UASB5.95 mg L−1No significant inhibition[102]
ZnSerum flask20.0 mg L−1Activity decreased by 20.1%[57]
UASB25 mg L−1Inhibition by 50%[103]
HgSerum vials60.35 mg L−1Inhibition by 50%[104]
Ag11.52 mg L−1
Cd11.16 mg L−1
MnSerum vials175.8 mg L−1Inhibition by 50%[105]
UASB: upflow anaerobic sludge bed; MBBR: moving bed biofilm reactor; SBR: sequencing batch reactor; RBC: rotating biological contractor.
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Deng, W.; Wang, L.; Cheng, L.; Yang, W.; Gao, D. Nitrogen Removal from Mature Landfill Leachate via Anammox Based Processes: A Review. Sustainability 2022, 14, 995. https://doi.org/10.3390/su14020995

AMA Style

Deng W, Wang L, Cheng L, Yang W, Gao D. Nitrogen Removal from Mature Landfill Leachate via Anammox Based Processes: A Review. Sustainability. 2022; 14(2):995. https://doi.org/10.3390/su14020995

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Deng, Weifeng, Litao Wang, Lang Cheng, Wenbo Yang, and Dawen Gao. 2022. "Nitrogen Removal from Mature Landfill Leachate via Anammox Based Processes: A Review" Sustainability 14, no. 2: 995. https://doi.org/10.3390/su14020995

APA Style

Deng, W., Wang, L., Cheng, L., Yang, W., & Gao, D. (2022). Nitrogen Removal from Mature Landfill Leachate via Anammox Based Processes: A Review. Sustainability, 14(2), 995. https://doi.org/10.3390/su14020995

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