18 research outputs found

    Biological sulphate reduction with primary sewage sludge in an upflow anaerobic sludge bed reactor – Part 6: Development of a kinetic model for BSR

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    A 2-phase (aqueous-gas) kinetic model for biological sulphate reduction (BSR) using primary sewage sludge (PSS) as carbon source is presented. The methanogenic anaerobic digestion (AD) model of Sötemann et al. (2005) is extended by adding the biological, chemical and physical processes associated with BSR, i.e. propionic acid degrading sulphate-reducing bacteria (SRB), acetoclastic SRB and hydrogenotrophic SRB, the aqueous weak acid/base chemistry processes of the sulphate and sulphide systems and an aqueous-gas sulphide exchange process. The model is validated with experimental data from 2 upflow anaerobic sludge bed (UASB) reactors fed various PSS COD/SO42- ratios under constant flow and load conditions at 35°C and 20°C. The kinetic model results, including the reactor pH (within 0.1 pH unit) compare well with the experimental results and with those calculated from a steady-state BSR model. The kinetic model confirms that: (1) at ambient temperature (20°C), the hydrolysis rate is significantly reduced compared with that at 35°C, which requires a longer sludge age (larger bed volume) in the UASB reactor; (2) the hydrolysis rate of the PSS biodegradable particulate organics (BPO) is the same under methanogenic and sulphidogenic conditions; (3) the PSS BPO are carbon deficient for BSR in that more electrons are donated than carbon supplied for the required alkalinity increase, with the result that the sulphide system supplies the alkalinity deficit; and (4) due to (3) there is zero CO2 gas generation and in effect the sulphide system establishes the reactor pH. This observation allows the carbon content of the utilised organics to be determined from the H2CO3* alkalinity increase in the reactor, which can be simply measured by titration methods. Keywords: biological sulphate reduction, primary sewage sludge, upflow anaerobic sludge bed reactor, dynamic model, kinetics, stoichiometry, mixed weak acid/base chemistr

    Biological sulphate reduction with primary sewage sludge in an upflow anaerobic sludge bed reactor – Part 5: Steady-state model

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    This paper describes the development of a steady-state anaerobic digestion model for biological sulphate reduction using primary sewage sludge (PSS) as substrate. The model comprises: a chemical oxygen demand (COD) based hydrolysis kinetics part in which the PSS biodegradable COD and sulphate removals are calculated for given hydraulic and sludge retention times; a C, H, O, N, P, S, COD and charge mass balance stoichiometry part in which the alkalinity generated (from both the HCO3- and HS-) is determined from the COD and sulphate removals; and an inorganic carbon (CO2) and sulphide mixed weak acid/base chemistry part in which the digester pH is calculated from the HCO3- and HS- species formed. From the stoichiometry, it was found that the PSS is carbon limited in that it does not generate sufficient HCO3- alkalinity for the sulphate reduction, i.e., its COD/C ratio is too high which accounts for the observed zero gas (CO2) generation. The H2S/HS- system provides the alkalinity shortfall and establishes the system pH. Once developed and calibrated, the model results were compared with experimental data from 2 laboratory-scale upflow anaerobic sludge bed reactors (operated at 35oC and 20°C respectively) fed PSS and sulphate. The predicted COD and sulphate removals, alkalinity and digester pH correspond very well to the measured data. The model assists in identifying design and operation parameters sensitive to the system and provides a basis for developing an integrated biological, chemical and physical process dynamic model. Keywords: biological sulphate reduction, primary sewage sludge, upflow anaerobic sludge bed reactor, steady state model, kinetics, stoichiometry, mixed weak acid/base chemistr

    Application of the activated sludge model to aerated lagoons

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    The different kinds of aerated lagoons, which exclude anaerobic pre-treatment ponds, are described and the design approach for aerated lagoons is explained. This hinges around ensuring that the 1st lagoon is suspension mixed and the second and any additional are facultative. Selection of the retention time for the 1st lagoon is important to ensure complete utilization of the influent biodegradable organics. Minimum retention times to achieve this at 14°C and 22°C were determined with the general activated sludge kinetic simulation model for (i) readily biodegradable soluble organics (BSO) only, (ii) slowly biodegradable particulate organics (BPO) only, (iii) real municipal wastewater (20% BSO and 80% BPO) and (iv) real municipal wastewater with 5% OHO active VSS mass seed. The minimum hydraulic retention times for these four cases are: at 14°C 1.3, 3.0, 2.0 and 1.5 d, respectively, and at 22°C 0.3, 2.0, 1.2 and 1.0 d, respectively. From a comparison of the simulation results with the steady-state model calculations, washout of OHOs takes place at about 75% of these retention times. Approximate equations to estimate the power requirements for aeration by mechanical surface aerators and mixing are given. These equations are combined with those of the steady-state activated sludge lagoon model for calculating the oxygen requirements and the aeration power density (W/m3) in each lagoon. With these equations, it is shown that influent COD concentration needs to be between an upper and lower limit band to ensure that the 1st lagoon is suspension mixed and the second lagoon is facultative. This COD concentration band decreases as the influent flow increases. The important conclusion arising from this is that if the aerated lagoon system is applied for small rural communities, where land for these large systems is likely to be available, then additional mixing energy above that for aeration will need to be provided to ensure that the 1st lagoon is suspension mixed – this additional aeration cost makes it unlikely that aerated lagoons will be applied for municipal wastewater treatment. Matching mixing and aeration power requirements for industrial organic wastewaters is easier because these usually are significantly stronger than municipal wastewaters
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