Escherichia coli inactivation kinetics in anaerobic digestion of dairy manure under moderate, mesophilic and thermophilic temperatures
Pramod K Pandey
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Michelle L Soupir
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Agricultural and Biosystems Engineering Department, Iowa State University
, Ames, 50011,
USA
Batch anaerobic digestion experiments using dairy manure as feedstocks were performed at moderate (25C), mesophilic (37C), and thermophilic (52.5C) temperatures to understand E. coli, an indicator organism for pathogens, inactivation in dairy manure. Incubation periods at 25, 37, and 52.5C, were 61, 41, and 28 days respectively. Results were used to develop models for predicting E. coli inactivation and survival in anaerobic digestion. For modeling we used the decay of E. coli at each temperature to calculate the first-order inactivation rate coefficients, and these rates were used to formulate the time - temperature - E. coli survival relationships. We found the inactivation rate coefficient at 52.5C was 17 and 15 times larger than the inactivation rate coefficients at 25 and 37C, respectively. Decimal reduction times (D10; time to achieve one log removal) at 25, 37, and 52.5C, were 9 -10, 7 - 8 days, and < 1 day, respectively. The Arrhenius correlation between inactivation rate coefficients and temperatures over the range 25 -52.5C was developed to understand the impacts of temperature on E. coli inactivation rate. Using this correlation, the time - temperature - E. coli survival relationships were derived. Besides E. coli inactivation, impacts of temperature on biogas production, methane content, pH change, ORP, and solid reduction were also studied. At higher temperatures, biogas production and methane content was greater than that at low temperatures. While at thermophilic temperature pH was increased, at mesophilic and moderate temperatures pH were reduced over the incubation period. These results can be used to understand pathogen inactivation during anaerobic digestion of dairy manure, and impacts of temperatures on performance of anaerobic digesters treating dairy manure.
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Introduction
In the United States, combined livestock production of
cattle, swine, and sheep generates 49% of the total farm
income, which is nearly 241 billion dollars (US Census
Bureau 2010,). The practice of applying livestock
manure to recycle waste to enhance crop yield is more than
4,000 years old, and this practice continues to reduce
farm fertilization costs in the developing as well as the
developed world (WHO 2010,; USEPA 2010,). However,
land application of manure can damage environmental
ecosystems (USEPA, 2010,) and create a risk to human
health if not applied properly. Runoff from fields where
manure has been applied can be a source of pathogen
contamination in ambient water bodies including
streams lakes and reservoirs and groundwater systems
(Brennan et al. 2010,; Gerba and Smith 2005,; Mawdsley
et al.1995,; Pell 1997,; Tyrrel and Quinton 2003,; Unc
and Goss 2004,), particularly if a rainfall event occurs
soon after application (Soupir et al. 2006).
Manure can contain numerous pathogenic organisms
that are associated with human diseases including
salmonella, E. coli O157:H7, Yesinia, campylobacter,
guardia, and cryptosporidium (Klein et al. 2010,; Ltourneau
et al. 2010,; Mass et al. 2010,; Ziemer et al. 2010,).
Treating manure before land application can greatly
reduce the number of viable pathogens, and various
methods such as drying (Amin-Nayyeri et al. 2010,),
composting (Maeda et al. 2010,), heat treatment
(Shepherd Jr et al. 2010,), radiation treatment (Farag and
Mohamed 1999,; Sinton et al. 2007,), aerobic digestion
(Bortone 2009,; Dumas et al. 2010,; Shen et al. 2010,),
and anaerobic digestion (Aitken et al. 2005,; Aitken et
al. 2007,; Lang and Smith 2008,; Popat et al. 2010,; Sung
and Santha 2003,; Wagner et al. 2009) are typically used.
Of these, anaerobic digestion is crucial as it produces
biogas, a source of energy, in addition to reducing
pathogens.
The use of anaerobic digesters for biogas production
and manure treatment is well established and has been
implemented all over the world. A tremendous amount
of research has been conducted on the anaerobic
digestion process to enhance biogas production (Climent et
al. 2007,; He et al. 2008,; Kim et al. 2010,; Pandey et al.
2010,; Yilmaz and Demirer 2008,; Zaher et al. 2008,),
increase nutrient recovery (Banu et al. 2009,; Carrere et
al. 2010,; Jin et al. 2009,; Novak et al. 2010,;
Prapaspongsa et al. 2010,; Wang et al. 2010,), and reduce solids
content (Forster-Carneiro et al. 2010,; Gilroyed et al.
2010,; Gong et al. 2010,; Riau et al. 2010,; Rubio-Loza
and Noyola 2010).
Batch reactors are a useful tool to improve
understanding of the outcomes of anaerobic digestion
processes. Masse et al. (2010) evaluated efficiency of
commercial-scale psychrophilic anaerobic digestion in
sequencing batch reactors, operated at 7 or 14 days
hydraulic retention time and 24C. The authors found
that the concentrations of fecal coliforms, E. coli,
Salmonella, Campylobacter spp., and Y. enterocolitica were
reduced to undetectable levels in pig manure. Ct et al.
(2006) found nearly complete reduction of total
coliforms and E. coli by anaerobic digestion at 20C for 20
days while Baert et al. (2010) observed a 4 log decrease
of Murine Norovirus-1 at 37 and 52C after 13 and 7
days, respectively. Several studies have focused on
pathogen inactivation in sludge anaerobic digestion at
thermophilic temperatures to achieve Class A (complete
pathogen inactivation) and Class B (incomplete
pathogens removal) classification (Aitken et al. 2005,; Popat et
al. 2010,; Puchajda et al. 2006,; Smith et al. 2005,;
Wagner et al. 2009,). For example, Shin et al. (2010),
used the batch process to show decreases in bacteria
16S rRNA gene concentrations and organic removal
efficiency in anaerobic digestion of secondary sludge, while
Aitken et al. (2005) measured the inactivation of vaccine
- strain poliovirus and eggs from helminth Ascaris suum
at temperatures from 49 to 55C in biosolids. Popat et
al. (2010) used the batch process to estimate the
inactivation kinetics of Ascaris suum and poliovirus type 1
(PVS -1) at temperatures ranging from 51 to 56C.
Despite previous studies to determine pathogen decay
under anaerobic conditions, no information exists on
the performance of anaerobic digestion in reducing
pathogen concentrations in dairy manure.
Aitken et al. (2005), and Popat et al. (2010) provided
important information about pathogen inactivation
kinetics in anaerobic digestion. However, both of these
studies are focused on anaerobic digestion of sludge
obtained from municipal waste treatment facilities, and
inactivation kinetics were determined at temperatures
ranging from 49 to 56C (thermophilic). Both studies
emphasized the need for improving EPAs time -
temperature relationships. Our objective is to determine the
E. coli inactivation kinetics in dairy manure at moderate
(25C), mesophilic (37C) and thermophilic (52.5C)
temperatures, and use the inactivation kinetics at these
temperatures to derive the time - temp (...truncated)