The product of the biological sulphate reduction is sulphide. High concentrations of molecular H 2 S (g) can be inhibitory for microbial activity, especially at a reactor pH of 6 to 7. This paper focuses on the effect of high sulphide concentrations on the sulphate reduction rates. The results of three investigations operating a continuous reactor, a column reactor and batchtest reactors have shown that increased sulphide concentrations have resulted in improved biological sulphate reduction. In all instances the reactor pH was kept at 7.5 to 8.5. It was shown that when the sulphide concentration was 700 mg/ℓ in a continuously operated reactor, the sulphate reduction rate was 12 gSO 4 /ℓ•d. When operating batch-test reactors the results showed that when the sulphide concentration increased, to 1 400 mg/ℓ, the volumetric and specific sulphate reduction rates correspondingly increased to 4.9 gSO 4 /ℓ•d and 1.5 gSO 4 /gVSS, respectively. Thirdly, operating a tall column reactor using H 2 and CO 2 as the energy source, showed that when the initial sulphide concentration of the feed water was 0, 100 and 268 mg/ℓ, the average biological sulphate removals were 650, 1 275 and 1 475 mg/ℓ, respectively. These obtained results indicated that the addition of sulphide to the feed water to the reactor had a positive effect on sulphate removal. Improved sulphate removal results in increased alkalinity production and in an increased reactor pH, which in turn is favourable for a decrease in the redox potential, when a dominant redox couple, like sulphate: sulphide, is present in a reactor.
The use of chemical coagulants and flocculants to supplement chemically enhanced primary treatment (CEPT) processes is increasing in popularity as it has been demonstrated to improve carbon redirection and suspended solids and phosphorus removal. Dosing 15 mg ferric chloride/L of wastewater and poly aluminum chloride (PACl; 0.5 mg/L) to the influent of a primary clarifier successfully achieved improved carbon redirection and suspended solids removal at a full‐scale WWTP. In this study, the impacts of PACl on the downstream liquid and solid train processes of the same WWTP were investigated. Compared to FeCl3 addition, a combined PACl and FeCl3 addition to the primary influent reduced the TSS and TP concentrations of the secondary clarifier effluent by 20% and 33%, respectively. Effluent BOD5 and ammonia‐nitrogen concentrations of the downstream activated sludge process were not affected by the addition of a combined FeCl3 and PACl in the primary clarifier. PACl addition affects the bioavailability of carbon and hence reduced the methane production efficiency of the primary sludge by 20%–30%. However, the significant amount of carbon concentrated in the CEPT sludge would enhance the amount of energy recovered through incineration. Practitioner points The chemically enhanced primary treatment process is an attractive method for carbon redirection and energy recovery. The combined FeCl3 and PACl addition in the primary clarifier improves the full scale activated sludge process effluent quality. PACl has a negative effect on methane production.
There has been increased interest towards maximizing wastewater energy recovery by enhancing the carbon captured through the primary treatment process such as chemically enhanced primary treatment (CEPT). This research was conducted to optimize the CEPT performance in terms of redirection of carbon and nutrients in both bench- and full-scale operations. In order to improve the CEPT process, the performance of ferric chloride and seven types of polymers were evaluated through jar testing. The optimal coagulant (15 mg/L ferric chloride) and flocculant (0.5 mg/L poly aluminum chloride (PACl)) combination achieved total COD, soluble COD, total suspended solids (TSS), and total phosphorus (TP) removal efficiencies of 76, 58, 89, and 84, respectively, in a full-scale primary clarifier operation. In doing so the organic matter and phosphorus were concentrated in CEPT sludge, making them available for recovery. Furthermore, the relationship between influent characteristics and removal rates under varying operating conditions was investigated. It was found that soluble COD removal appeared to be season-dependent, and TSS removals were independent of influent TSS concentrations in all scenarios. The removal of tCOD, sCOD, and TP had a positive relationship with their corresponding concentrations when the polymer Alcomer® 120L was used, whereas no correlation between removal and concentration was observed with PACl.
The potential for integrated fixed film activated sludge (IFAS) processes to achieve enhanced transformation of pharmaceuticals relative to conventional activated sludge (CAS) processes was assessed. Previous studies have focused on direct comparisons of parallel reactors with and without fixed film carriers and little information is available on the impacts of how varying operating parameters impact the differences in observed pharmaceutical compound (PC) transformation capabilities between CAS reactors and those equipped with both an activated sludge (AS) and fixed film carriers. The testing was carried out using bench scale sequencing batch reactors fed with authentic municipal wastewater and operated at selected combinations of temperature and solids retention time (SRT). PC transformation efficiencies were assessed in a 2 factorial design that employed the IFAS and CAS processes, operated in parallel under identical process conditions. Nitrification rate testing that was conducted to obtain insight into the biomass activity demonstrated that IFAS consistently had improved nitrification kinetics despite lower mixed liquor volatile suspended solids levels thereby demonstrating the contribution of the biofilm to nitrification. Increased transformation of atenolol (ATEN; ranging from 10-60%) and trimethoprim (TRIM; ranging from 30-50%) in the IFAS equipped reactors relative to their respective activated sludge (AS) controls was observed under all experimental conditions. Negligible transformation of carbamazepine was observed in both reactors under all conditions investigated. More than 99% of acetaminophen was transformed in both configurations under all conditions. There was no correspondence between nitrification activity and TRIM removal in the control AS while conditions that stimulated nitrification in the control AS also resulted in enhanced removal of ATEN. The results of this study indicate that the integration of biofilms in AS processes enhances transformation of some PCs.
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