Phosphorus Sequestration in Biosolids, Nuisance Struvite Control via PAD and Chemical Addition to TH-AD Digestate

Purpose: Struvite (MgNH4PO4*6H2O) and other precipitates have long posed persistent maintenance and operational challenges at wastewater treatment plants. These precipitates can be enhanced at plants that utilize biological phosphorus removal and can precipitate within anaerobic digesters and on final dewatering equipment which causes damage and decreases efficiency. Struvite can be sequestered as nutrient rich biosolids if properly controlled to remain in the cake. In a digested solids storage tank (DSST) that is in between anaerobic digestion and final dewatering, precipitation can be controlled by manipulating variables such as mixing, aeration of digestate to achieve a shorter solids retention time (SRT) version of post aerobic digestion (PAD) and by chemical addition. Optimizing this via batch and pilot testing can control nuisance struvite formation, increase phosphorus in the cake and achieve additional volatile solids reduction (VSR). This research will review findings from batch and pilot scale tests and discuss the nature of these precipitates. Objectives include determining the mechanism that provides optimal phosphorus removal, ammonia removal, and analyzing the precipitated solids of interest. The presentation will discuss results across batch, pilot, and full-scales and the lessons learned of each. Motivation and Background: The Atlantic Treatment Plant (ATP) in Virginia Beach, VA, operated by the Hampton Roads Sanitation District's (HRSD) is a high-rate facility with an A/O process configuration. In solids handling, a Cambi Thermal Hydrolysis Process (THP) is utilized prior to anaerobic digestion. ATP is actively engaged in efforts to control formation of scaling precipitates and nuisance struvite for optimal operational efficiency. Precipitate formation is determined predominantly by the solids solubility product (Ksp) and the saturation in solution and can be controlled by pH [1]. Manipulation of pH via CO2 stripping from aeration has successfully been shown to control solubility reactions [2, 3]. Increasing the saturation index via chemical addition can also control precipitation reactions and improve cake dryness with an SRT of a few hours [4]. Likewise, PAD has been shown to achieve ammonia removal and additional VSR at a 5-6 day SRT [5]. Based on these findings, a pilot scale set up (Figure 1) will run at an SRT of 3 days to provide benefits from PAD, but with a longer reaction time that may be more beneficial for phosphorus sequestration. Various mixing, aeration rates, and chemical addition will be manipulated to determine the optimal operation conditions on phosphorus sequestration in the class A biosolids. Pilot Design and Operation: The pilot set up at ATP consists of four tanks. Each tank has a volume of about 63 gallons. Simulating the DSST, the tanks are operated as daily batch fed continuously stirred tank reactors maintained by pump recirculation with a 3-day SRT. The tanks are aerated with fine bubble diffuser membranes which can be operated at constant or intermittent air flow rates, or via Dissolved Oxygen (DO) or pH set points. Preliminary operation has included mixing and aerating the four tanks at a constant airflow rate of 5 LPM, while recording online measurements of DO, pH (Figure 2), and temperature, which has been maintained between 22 and 38 degrees C. At this operation, about 50% OP removal and 10% COD degradation across the pilot has been measured with minimal NH3 removal. Future plans include operating at higher aeration rates, DO control setpoints, the potential establishment of partial nitrification/nitritation, and the addition of Ca(OH)2 or Mg(OH)2 at various dosages. Preliminary mixing operations conducted under suboxic conditions without the use of chemical addition results in a sustained OP removal by about half across the pilot. This suggests value in this continued effort. Batch Testing: The following test was conducted on a Phipps and Bird Jar Tester at a continuous mixing speed of 300 rpm. Five jars of digestate consisting of a control with no chemical addition, two jars dosed with a carbide lime slurry at Ca2+ + Mg2+/P ratios of 0.5:1 and 1:1, and two jars dosed with thioguard, at the same Ca2+ + Mg2+/P ratios. Chemical dose was injected as a spike at time zero of the test. Analytical measurement of OP-P and pH were determined daily via spectrophotometry (HACH TNTplus UHR mg-PO4-P/L and pH meter) (Figure 3). The pH of the digestate sample was about 7.4 and increased up to a maximum of 8.7 within 24 hours likely due to CO2 stripping from the mixing intensity. OP removal in the control condition was measured as 68%. The addition of chemical helped to increase OP removal as high as 95%. The digestate pH increasing towards alkaline within the first test day showed the greatest impact on OP removal rate. The higher Ca2+ + Mg2+/P molar ratio tested of 1:1 for both the chemicals had higher OP removal rates than those dosed at lower ratios of 0.5:1. Thioguard compared to the carbide lime slurry overall had a slightly more significant effect on OP removal. The pH decrease measured after 24 hours may be due to struvite's production of hydrogen ions in the formation reaction, however, future plans of repeat experiments and X-Ray Diffraction for precipitate analysis will further determine this.