Introduction
Swine raising has changed considerably in the last 30 years with an increase in intensive production systems. Whereas intensive systems minimize production costs, the high animal densities can pose impacts to environments that have low soil absorption capacity (Kunz et al., 2009a; Vanotti et al., 2009). Thus, confined animal feeding operations (CAFOs) while reducing the production costs can increase the use of water and the environmental impacts associated with the residues generated during production (Bradford et al., 2008).
The need for swine manure treatment is usually dependent on factors such as soil/plant nutrient absorption capacity and land availability. Nitrogen is usually the most critical compound that needs to be removed due to its relatively high concentrations, treatability limitations and high costs of removal (Vanotti and Szogi, 2008).
Conventional nitrogen removal technologies are commonly based on aerobic autotrophic nitrification (i.e., nitrification) followed by anoxic heterotrophic process (i.e., denitrification). The reactions involved in both steps are shown in Equations 1 to 4. These processes are generally performed using separate reactors and the carbon for denitrification is obtained from the organic matter in the swine effluent (Ahn, 2006; Zhu et al., 2008).
Treatment technologies should rely on the possibility of water reuse to minimize high quality water demand for barns washing and manure flush. A possibility that can be considered is to have the denitrification process occurring directly in the pits using the organic carbon present in raw manure. This strategy can reduce the costs of treatment facilities and clean water input for swine production (O´Connor et al., 2008; Vanotti et al., 2009). It avoids the use of high quality water for manure management, observing the biosecurity criteria, reducing the demand of water for swine production (Vanotti et al., 2005).
This study aimed to evaluate the potential for water reuse at swine barns as a strategy for denitrification enhancement and to study the effectiveness of nitrogen removal from swine wastewaters in swine facilities by simulating pit conditions and combining treated effluent with raw manure.
Materials and Methods
Sampling and storage
The raw swine manure used in this study was collected from an experimental swine production system located in Concórdia, Santa Catarina State, Brazil (27º18’ S, 51º59’ W). Raw manure produced in the first 24 h was collected directly from reception pits inside the finishing houses. Samples were prepared and stored according to Kunz et al. (2009b). Samples of treated effluent were collected from a swine manure treatment system (SMTS) also located in Concórdia (Kunz et al., 2009a). The samples were collected after an aerobic nitrification reactor and the biological sludge settling tank (Figure 1A) and homogenized with raw manure at different ratios.
Experimental design
To mimic the pit storage processes and investigate the denitrification potential after adding the nitrified effluent to raw manure, raw manure was mixed with treated effluent at different ratios [raw manure/ (raw manure + treated effluent)] of 1.0, 0.9, 0.8, 0.7, 0.6, 0.5 and 0 to simulate different reuse conditions. The mixed effluent was stored in triplicate in 20 L polyethylene buckets (Figure 1B) at room temperature during five days. From these stored buckets, 100 mL of the homogenized samples were collected every 24 hours and analyzed for pH, oxidation-reduction potential (ORP), ammonia (NH3 -N), nitrite (NO2 -N), nitrate (NO3 -N) and chemical oxygen demand (COD). All analyses were performed according to APHA (1995). NOx -N concentration was obtained by adding up NO2 -N and NO3 -N concentrations.
Results obtained at different mixing ratios of raw manure with treated effluent are important to help understand what will happen with the treated effluent when reused in the barns, especially for the fate of nitrogen. For instance, when reused to wash the swine facilities and flush the manure. In this study, raw manure was combined to treated effluent at different ratios varying from 0 to 50 % (v v–1). These dilution ratios are consistent with wastewater reuse, especially in Brazilian CAFOs, when considering the water demand for managing manure in the houses (Perdomo et al., 2003).
Data analysis
Nitrogen removal rates were estimated using linear regression of the raw manure/(raw manure + treated effluent) ratios according to Equation 5:
Where y is the observed value from the variables of interest (NO2 -N and ∑NOx -N) transformed into natural logarithm; α is the day zero concentration logarithm; β represents the degradation constant, t the time; e is the random error distributed independently and identified. The effect of β was tested by the F-test. The above model estimates the half-life of each effluent concentration from exponential first-order regression analyses as demonstrated in Equation 6 (Pedersen, 2009) and its confidence interval by t distribution. Data values equal to zero were neglected.
Results and Discussion
Variations in COD (Figure 2) and NH3 -N (Figure 3) concentrations were high for all mixture ratios tested. These variations were likely due to hydrolysis and dissolution caused by biodegradation of carbon-rich fresh manure (Kunz et al., 2009b, Markevich et al., 2010). Increasing ammonium concentrations lead to ammonification (free amino acids are produced by enzymatic protein hydrolysis) that is favored in reducing conditions (low ORP) (Figure 4) typically observed in swine effluents (Cantrell et al., 2008; Garcia and Angenent, 2009).
Except for treated effluent (ratio 0), pH decreased in all mixture ratios (Figure 5), probably due to substrate hydrolysis and formation of volatile fatty acids as byproducts from bacterial metabolism (Kashyap et al., 2003). For treated effluent, the content of organic matter is very low (Figure 2) favoring autotrophic processes like algae proliferation, which can be the responsible for pH increasing (Zanotelli et al., 2002).
NOx -N depletion was found when fresh manure was combined with the nitrified treated swine effluent (Figure 6). NOx -N species (NO3 -N + NO2 -N) reduction was observed (p < 0.0001) for all tested mixture ratios, except for ratios 0.9 and 1.0. Thus, NOx -N was not observed in the samples after 48 h of experiment for ratios between 0.6 and 0.8. NOx -N concentrations were not detected at all times at the 1.0 ratio. NO2 -N and NOx -N concentrations in raw manure were negligible due to the reducing conditions (Figure 4) that prevent generation of these oxidized species. For the 0.9 ratio, the NOx -N concentrations were close to the detection limit of chemical analysis for zero and one day and not detected for sequential times.
Table 1 shows the half-life for different raw manure and treated effluent ratios. Similar concentrations of NO2 -N and NOx -N were estimated using α from Equation 5. Although NOx -N was detected at the first days in the 0.9 treatment, the very low concentration did not allow for half-life estimation (p > 0.05). NO2 - N and NOx -N half-life, resulting from slope ( β ), were lower than 0.5 days for the treatments between 0.5 and 0.8 ratios.
If the reuse of treated effluent possibilities were considered in a commercial farm (eg, first pave cleaning and pit flushing), treatment 0.7 could be a reference. In this case, a very fast NOx -N decrease (half-life near 0.12 day) was observed, allowing conditions for NOx -N extinction in approximately 2 days.
The heterotrophic medium in raw manure offered good conditions for quick nitrogen removal under anoxic conditions. The chemical reducing conditions in raw manure, shown as negative ORP values in Figure 4, benefited NOx -N removal when mixed with nitrified effluent due to the oxidation of the organic carbon using nitrogen oxidized species as an electron acceptor (Gilbert et al., 2008; Vanotti and Szogi, 2008). Heterotrophic microorganisms have a very high growing rate which favors denitrification processes (Potter et al., 1998; Ahn, 2006). The specific growth rate (µmax) for NO3 – and NO2 – reduction are 2.6 d–1 and 1.5 d–1, respectively. These are significantly higher than µmax for nitrification (µmaxNH4 oxidation = 0.77 d–1 and µmaxNO2 – oxidation = 1.08 d–1) (Wiesmann, 1994).
Another factor that influences denitrification is the C/N ratio. For a good nitrogen removal efficiency, the C/N ratio must be higher than 3.5 (Grady Jr. et al., 1999; Ahn, 2006; Ginige et al., 2009). In this study (Table 2), the COD/NOx -N was extremely high for all mixtures and dates; they ranged from 89 to 43,514.
High C/N ratios can also hinder the generation of N2 O, an important greenhouse gas (Ravishankara et al., 2009) that is produced in low C/N ratio environments. Bernet et al. (1996) studied the denitrification of piggery wastewater and concluded that when TOC/N was between 1.6 and 2.4 (COD/N between 4.26 and 6.4), N2 O emission was observed, but when TOC/N was higher than 2.4, N2 O was not emitted. Itokawa et al. (2001) investigating the nitrous oxide production under low COD/N ratios conditions concluded that 20-30 % of the total influent nitrogen was emitted as N2 O with influent COD/N less than 3.5.
Conclusions
NOx -N can easily and quickly be removed from swine effluents by mixing raw manure with treated effluent. High NOx depletion due to denitrification was observed for all RM/(RM+TE) ratios tested with half-life less than 12 h which is within a reasonable time considering the manure management in the swine production facilities.
It is possible to remove nitrogen by carbon-rich manure degrading bacteria during denitrification. This can minimize the input of treated water in CAFOs by reusing the nitrified effluent at different ratios back in the barns for cleaning and flush the manure.
Acknowledgements
To Dr. Marcio L.B. da Silva, for his comments on an early draft. Airton Kunz and Simone Dasmasceno were financially supported by the Brazilian National Council for Scientific and Technological Development (CNPq).
This article was originally published in Scientia Agricola. v.69, n.6, p.352-356, November/December 2012. http://dx.doi.org/10.1590/S0103-90162012000600002. This is an Open Access article licensed under a Creative Commons Attribution License. References
Ahn, Y. 2006. Sustainable nitrogen elimination biotechnologies: a review. Process Biochemistry 41: 1709–1721.
American Public Health Association [APHA]. 1995. Standard Methods for the Examination of Water and Wastewater. 19ed. American Public Health Association, Washington, DC, USA.
Bernet, N.; Delgenes, N.; Moletta, R. 1996. Denitrification by anaerobic sludge in piggery wastewater. Environmental Technology 17: 293–300.
Bradford, S.A.; Segal, E.; Zheng, W.; Wang, Q.; Hutchins, S.R. 2008. Reuse of concentrated animal feeding operation wastewater on agricultural lands. Journal of Environmental Quality 37 (supplement): S-97–S-115.
Cantrell, K.B.; Ducey, T.; Ro, K.S.; Hunt, P.G. 2008. Livestock waste-to-bioenergy generation opportunities. Bioresource Technology 99: 7941–7953
Kashyap, D.R.; Dadhich, K.S.; Sharma, S.K. 2003. Biomethanation under psychrophilic conditions: a review. Bioresource Technology 87: 147–153.
Kunz, A.; Miele, M.; Steinmetz, R.L.R. 2009a. Advanced swine manure treatment and utilization in Brazil. Bioresource Technology 100: 5485–5489.
Kunz, A.; Steinmentz, R.L.R.; Ramme, M.; Coldebela, A. 2009b. Effect of storage time on swine manure solid separation efficiency by screening. Bioresource Technology 100: 1815– 1818.
Garcia, M.L.; Angenent, L.T. 2009. Interaction between temperature and ammonia in mesophilic digesters for animal waste treatment. Water Research 43: 2373–2382.
Gilbert, Y.; Bihan, Y.L.; Aubry, G.; Veillette, M.; Duchaine, C.; Lessard, P. 2008. Microbiological and molecular characterization of denitrification in biofilters treating pig manure. Bioresource Technology 99: 4495–4502.
Ginige, M.P.; Bowyer, J.C.; Foley, L.; Keller, J.; Yuan, Z. 2009. A comparative study of methanol as a supplementary carbon source for enhancing denitrification in primary and secondary anoxic zones. Biodegradation 20: 221–234.
Grady Jr., C.P.L.; Daigger, G.T.; Lim, H.C. 1999. Biological wastewater treatment. 2ed. Marcel Dekker, New York, NY, USA.
Itokawa, H.; Hanaki, K.; Matsuo, T. 2001. Nitrous oxide production in high-loading biological nitrogen removal process under low COD/N ratio condition. Water Research 20: 657–664.
Markevich, H.A.; Pell, A.N.; Mbugua, D.M.; Cherney, D.J.R.; Van Es, H.M.; Lehmann, M.; Robertson, J.B. 2010. Effects of storage methods on chemical composition of manure and manure decomposition in soil in small-scale Kenyan systems. Agriculture, Ecosystems & Environmental 139: 134–141.
O’Connor, G.A.; Elliot, H.A.; Bastian, R.K. 2008. Degraded water reuse: an overview. Journal of Environmental Quality 37 (supplement): S-157–S-169.
Pedersen, L.; Pedersen, P.B.; Nielsen, J.L.; Nielsen, P.H. 2009. Peracetic acid degradation and effects on nitrification in recirculating aquaculture systems. Aquaculture 296: 246–254.
Perdomo, C.C.; Oliveira, P.A.V.; Kunz, A. 2003. Suggested methodology to estimate volume and pollutant load in a swine production farm. Embrapa Suínos e Aves, Concórdia, SC, Brazil. 6p. (Comunicado Técnico, 332) (in Portuguese).
Potter, T.G.; Tseng, C.; Koopman, B. 1998. Nitrogen removal in a partial nitrification/complete denitrification process. Water Environmental Research 70: 334–341.
Ravishankara, A.R.; Daniel, J.S.; Portmann, R.W. 2009. Nitrous oxide (N2 O): the dominant ozone-depleting substance emitted in 21st century. Science 326: 123–125.
Vanotti, M.B.; Millner, P.D.; Hunt, P.G.; Ellison, A.Q. 2005. Removal of pathogen and indicator microorganisms from liquid swine manure in multi-step biological and chemical treatment. Bioresource Technology 96: 209–214.
Vanotti, M.; Szogi, A.; Bernal, M.P.; Martinez, J. 2009. Livestock waste treatment systems of the future: A challenge to environmental quality, food safety, and sustainability. Bioresource Technology 100: 5371–5373.
Vanotti, M.; Szogi, A. 2008. Water quality improvements of wastewater from confined animal feeding operations after advanced treatment. Journal of Environmental Quality 37: S86–S96.
Wiesmann, U. 1994. Biological nitrogen removal from wastewater. Advances in Biochemical Engineering/Biotechnology. Springer, Berlin, Germany.
Zanotelli, C.T.; Medri, W.; Belli Filho, P.; Perdomo, C.C.; Mulinari, M.R.; Costa, R.H.R. 2002. Performance of a baffled facultative pond treating piggery wastes. Water Science and Technology 45: 49–53.
Zhu, G.; Yongzhen, P.; Baikun, L.; Guo, J.; Yang, Q.; Wang, S. 2008. Biological removal of nitrogen from wastewater. Reviews of Environmental Contamination and Toxicology 192: 159–195.