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D S Mavinic

Publications and source records attributed to D S Mavinic.

8 recordsLinked to original sources

Production and basic morphology of struvite crystals from a pilot-scale crystallization process.

A pilot-scale, struvite crystallization process was operated using anaerobic digester supernatants from two, full-scale, treatment plants as influent. It was found that the produced struvite crystals were easily separated from the process and were composed of very pure struvite (91.2 % to 94.1 % purity), with small amounts of calcium and carbonate, and traces of iron and aluminum. Most of the harvested struvite crystals, which were an aggregation of numerous fine crystals, were round, hard and larger than 1.5 mm in mean diameter. The crystal retention time in the reactor and the magnesium dosage in the supernatant appeared to have a significant effect on the crystal size, hardness and morphology.

Crystallization↗

Exploring the determination of struvite solubility product from analytical results.

The solubility of magnesium ammonium phosphate hexahydrate (struvite) was determined in different water and wastewater solutions, by using the analytical results of the solubility tests conducted in the Environmental Engineering Lab at the University of British Columbia. The various factors affecting the struvite solubility such as pH, ionic strength and the temperature of the solutions were also studied in this project. The struvite solubility product values were found to vary significantly from one solution to another and over the range of the experimental conditions as well. For instance, the solubility product (Ksp) determined at 20 degrees C for anaerobic digester supernatant from the Penticton, B.C. Advanced Wastewater Treatment Plant, was found to vary from 8.46 x 10(-15) (pKsp =14.07) to 1.3 x 10(-13) (pKsp =12.89), over a pH range 6.45 to 8.97; while in the case of distilled water, with the same struvite crystals and at the identical temperature, it was found to vary from 5.21 x 10(-15) (pKsp=14.28) to 2.12 x 10(-13) (pKsp =12.67) over a pH range of 7.01 to 9.62. These results explore the possible reasons for widely varying struvite solubility reported in the literature. A possible correlation was also developed to correlate struvite solubility product with varying temperature. Furthermore, an attempt was made to establish a correlation between conductivity and calculated ionic strength of the solutions. A significant gap, between the values predicted by the correlation developed in this study and those predicted by the existing correlation, was also observed.

Bacteria, Anaerobic↗

Missing aerobic-phase nitrogen: The potential for heterotrophic reduction of autotrophically generated nitrous oxide in a sequencing batch reactor wastewater treatment system.

Several biochemical pathways can induce nitrogen loss from aerated, aerobic wastewater treatment bioreactors. These pathways include "traditional" simultaneous nitrification-denitrification (SND) (i.e. autotrophic nitrification - heterotrophic denitrification), autotrophic denitrification, and anaerobic ammonia oxidation. An oxygen limitation, often expressed in terms of low dissolved oxygen (DO) concentration, is a common element of these pathways. The presented research investigated the effect of mixed liquor DO concentration and biomass slowly degradable carbon (SDC) utilization rate on the heterotrophic nitrous oxide (N2O) reduction rate, for biomass cultured in an anoxic/aerobic wastewater treatment bioreactor. Biomass oxygen and SDC availability-limitation, expressed in terms of DO concentration and SDC ultilization rate, respectively, were found to significantly impact the observed heterotrophic N2O reduction rate. The findings support the hypothesis that nitrogen lost from the mixed liquor of an aerobic bioreactor could result from simultaneous autotrophic N2O generation (i.e. autotrophic denitrification) and heterotrophic N2O reduction. The results also support the idea that autotrophic N2O generation could be occurring in a bioreactor, although N2O may not be measurable in the reactor off-gas. Therefore, this autotrophic N2O generation - heterotrophic N2O reduction mechanism provides an alternative explanation to nitrogen loss, when compared to "conventional" SND, where heterotrophic organisms are assumed to reduce autotrophically generated nitrite and nitrate to dinitrogen (N2). In addition, nitrogen loss speculatively attributed to N2 formation via anaerobic ammonia oxidation in oxygen-limited environments, again because of the absence of measurable N2O, may in fact be due to the autotrophic N2O generation - heterotrophic N2O reduction mechanism.

Aerobiosis↗

Process control and design considerations for methanol-induced denitrification in a sequencing batch reactor.

The primary goal of this research was to determine the effect of methanol-induced denitrification on volatile suspended solids production, settleability, and oxidation-reduction potential in a full-scale sequencing batch reactor. Batch tests were also conducted to determine the influence of mixing and acclimatization on the denitrification of wastewater with methanol. The observed sludge production in the full-scale sequencing batch reactor with methanol addition was 0.21 kg volatile suspended solids l(-1) methanol, versus the calculated stoichiometric sludge production of 0.17 kg volatile suspended solids l(-1) methanol. The settleability in the full-scale sequencing batch reactor, measured by the sludge volume index, increases linearly with increasing denitrification rate. The total change in the oxidation-reduction potential magnitude during a sequencing batch reactor cycle increased linearly with increasing denitrification rate. A minimum of 55% increase in the denitrification rate was observed in a batch reactor with methanol addition and a sludge acclimatized to methanol addition, compared to a batch reactor with methanol addition and a non-acclimatized sludge. The non-acclimatized batch reactor had a negligible denitrification rate without methanol addition. However, significant denitrification rates were observed in the acclimatized batch reactors without methanol addition, potentially caused by microbial storage or an increased population of denitrifiers that scavenge any available carbon. A completely mixed batch reactor, with sludge acclimatized to methanol addition during the anoxic cycle, had an increase in the denitrification rate ranging from 660%, without methanol addition, to 200%, with a methanol dosage of 12.7 mg l(-1), compared to the unmixed batch reactor with an acclimatized sludge. Therefore, mixing appears to be critical to the denitrification process, to realize the best kinetic performance.

Bioreactors↗

Pollution reduction at wastewater treatment facilities through thermophilic sludge digestion.

Wastewater treatment facilities produce large amounts of sludge, which is a pollutant to the environment if not properly managed. Among the three most common methods (landfills, land application, incineration) of sludge disposal, thermophilic digestion to produce Class-A biosolids for land application is recognized as the most cost-effective, environmentally sustainable option. Full-scale experience revealed that thermophilically digested biosolids consumed a higher dosage of chemicals for conditioning and dewatering than conventionally (mesophilically) digested biosolids. This paper presents findings of a recent study to investigate how major operational parameters affect dewatering properties of thermophilically digested biosolids, and to search for the inter-relationship between digestion, characteristics of digested biosolids, and dewatering properties of thermophilic biosolids. Experimental work was carried out using bench-scale aerobic digesters. This study found that feed sludge composition has a significant effect on dewaterability. A higher content of secondary sludge resulted in poorer dewaterability in undigested and digested sludge. Dewatering properties are sensitive to a temperature effect. Such an effect is physical-chemical in nature. Excessive high shear results in significant deterioration in dewaterability. Thermophilic digestion resulted in a substantial increase in ammonia and phosphate concentrations, but these two factors seem to not have much impact on dewaterability. Instead, cellular biopolymers have a significant role in affecting dewatering properties of thermophilically digested biosolids.

Biopolymers↗

Impact of hydrogen peroxide oxygen transfer tests on the performance of the biological nutrient removal process.

Knowledge of in-process oxygen transfer is essential to the optimum design and operation of aeration systems in activated sludge processes. In this study, non-steady state H2O2 oxygen transfer tests were performed in a laboratory scale, University of Cape Town configuration biological nutrient removal process (BNR) to measure the in-process oxygen transfer rates. Given the small quantity (about 1 ml @30% concentration) of H2O2 used in the aerobic reactor with a mixed liquor volume of 161 (total system working volume of 33.65 l), no effect on the process performance itself was expected. However, the process performance data obtained indicated results to the contrary. Use of H2O2 in measuring process oxygen transfer rates may not be suitable for BNR processes, as all the major process performance indicators (carbon, nitrogen and phosphorus removal by the system and carbon uptake and phosphorus release in the anaerobic zone) were negatively affected. Evidence in thiswork leads to the conclusion that external addition of H2O2 leads to excessive production of the hydroxyl radical. Since microorganisms do not have enzyme systems capable of acting upon this additional reactive radical, it resulted in loss of process performance. It is also possible that H2O2 could have upset the normal aerobic respiration process by introducing oxidative stress conditions on the catalase, peroxidase and superoxide dismutase enzymes that deal with other oxygen radicals generated as part of the overall process of reducing oxygen to water. Any test that interferes with the system in which the test is being performed is suspect. Therefore, in light of these results, the H2O2 method to test in-process oxygen transfer should be re-evaluated.

Bacteria, Aerobic↗

The effect of decreased ambient temperature on the biological nitrification and denitrification of a high ammonia landfill leachate.

This research investigated the nitrogen removal capabilities of a pre- and post-denitrification process, when treating sanitary landfill leachate containing an ammonia concentration of over 2200 mg N/L, at operating temperatures down to 10 degrees C. The treatment system employed is generally known as a 4-Stage Bardenpho process. Two parallel systems were operated throughout the study; each system had an aerobic solids retention time of 20 days and an external recycle ratio (return activated sludge) of about 3:1. During the entire experimental period, one system used an internal recycle ratio of about 4:1, while the other system used one of 3:1. Methanol was used as supplementary carbon source for denitrification. When operating temperature was decreased from 20 to 17 degrees C, an approximate 15% decrease in denitrification was immediately experienced within both systems, with no noticeable affect on nitrification. This was an unexpected result. Subsequently, the temperature was further decreased to 14 degrees C, and finally to 10 degrees C. With the temperature at 14 degrees C, aerobic wasting was also stopped and methanol loading was progressively decreased to match actual denitrification requirements. At 10 degrees C, both systems suffered major nitrification and denitrification inhibition. Changes in operating parameters, such as a decrease in influent ammonia and methanol loading, as well as an increase in ambient temperatures, from 10 to 15 degrees C, did not significantly improve overall system performance, within a reasonable time frame. Both denitrification and nitrification problems were mainly attributed to decreased ambient temperature, although other possible factors were noted; at project completion, about 50% of the incoming ammonia was being removed across the system.

Aerobiosis↗

A pre- and post-denitrification system treating a very high ammonia landfill leachate: effects of pH change on process performance.

The prime objective of this research was to investigate the nitrogen removal capabilities of a pre- and post-denitrification process, when treating landfill leachate containing an ammonia concentration of over 2,200 mg N l(-1). The treatment system, also known as a 4-Stage Bardenpho process, was operated with an external recycle ratio of 3:1 and an internal recycle ratio of 4:1. The first anoxic reactor actual hydraulic retention time was 1.5 hours, while the first aerobic retention time was 3 hours. The very high ammonia concentration was simulated by pumping ammonium chloride into the first anoxic reactor of the system. Methanol was used as the organic carbon source for denitrification. At an influent ammonia concentration of about 2,200 mg N l(-1), the anoxic pH levels stabilized at about 8.6 within the first reactor, and at about 9.8 within the second reactor. These high anoxic pH levels were partially responsible for decreased denitrification and, hence, residual NO concentrations in the effluent. By decreasing the pH in the anoxic basins, the overall performance of the system immediately improved; the effluent NOx concentration decreased rapidly over a period of about six days, from an average 80 mg N l(-1) to about 60 mg N l(-1), with some samples as low as 40 mg N l(-1). Subsequently, increased leachate toxicity resulted in an unexpected system failure; although the treatment system eventually recovered and stabilized, denitrification in each anoxic reactor remained at only about 55%, with final effluent NOx concentrations of over 100 mg N l(-1). Despite this reduced level of performance, the decrease in anoxic pH resulted in enhanced nitrification performance, complete ammonia removal in the first aerobic reactor, and a more stable, overall performance in the 4-Stage Bardenpho process.

Ammonia↗