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Removal of pharmaceuticals in source-separated urine is an important step toward gaining acceptance of urine-derived fertilizers among important stakeholders such as consumers, farmers, and regulatory agencies. Advanced oxidation processes (AOPs) have been studied for the removal of pharmaceuticals in various complex matrices, including treated wastewaters. A complexity associated with AOP methods that rely primarily on hydroxyl radicals as the oxidizing agents is that they readily lose effectiveness in the presence of scavengers. Here, we investigated the potential for capturing the synergistic effects of producing multiple oxidative chemical species simultaneously in a plasma reactor to oxidize six pharmaceuticals (acetaminophen, atenolol, 17α-ethynyl estradiol, ibuprofen, naproxen, and sulfamethoxazole) in source-separated urine being processed into a fertilizer. The results show that the plasma reactor produced hydroxyl radicals as the primary oxidizing agent and the effects of other oxidizing species were minimal. Plasma experienced scavenging in both fresh and hydrolyzed urine; furthermore, it oxidized pharmaceuticals at similar rates across both matrices. Additionally, the negative impacts of electrical discharge formation stemming from increased solution conductivity appeared to plateau. The energy required per order of magnitude of pharmaceutical transformed was up to 2 orders of magnitude higher for plasma than for a traditional UV/H 2 O 2 reactor and depended upon the matrix. Despite scavenging and energy concerns, plasma can oxidize pharmaceuticals in fresh and hydrolyzed urine and is worthy of further development for on-site or building-scale applications where the value of convenience, simplicity, and performance offsets energy efficiency concerns. 

Ensuring long-term access to nutrients needed for food production is a growing global challenge. Human urine diversion and recycling is a viable and energy-efficient means of recovering nitrogen, phosphorus, and potassium from wastewater. Before implementation, however, it is critical to understand how communicating differently about human urine-derived fertilizer may influence its public acceptance. This study tests how different strategies of communication (video compared to texts), as well as different amounts of information, impact public acceptance. We also explored how specific characteristics, such as age and education level, may impact the usefulness of the different strategies of communication. The results indicate that short and long videos are the most useful risk communication strategies, and age fully moderates this relationship. This research may serve as a jumping off point for future studies focused on how risk communication strategies may affect consumer acceptance of other emerging food technologies. 

Pharmaceuticals and personal care products (PPCPs) can enter agricultural fields through wastewater irrigation, biosolid amendments, or urine fertilization. Numerous studies have assessed the risk of PPCP contamination, however there are no standardized methodologies for sample treatment, making the interpretation of results challenging. Various time periods between sampling and analysis have been reported (shipping, storage, etc. ), but literature is lacking in the evaluation of PPCP degradation amidst this process. This study assessed the stability of 20 pharmaceuticals (200 μg L −1 ) in soil and crops stored at −40 °C for 7, 30, and 310 days. After 310 days, caffeine, meprobamate, trimethoprim, primidone, carbamazepine, anhydro-erythromycin and dilantin were found to be stable (≥75% recovery) in all matrices. On the other hand, acetaminophen, amitriptyline, bupropion, lamotrigine, sulfamethoxazole, naproxen, ibuprofen, and paroxetine were unstable after 30 days in at least one of the matrices investigated. Due to variations in analyte stability, fortification with isotopically-labelled surrogates at the point of sample collection was evaluated in comparison to fortification after shipment and storage, immediately prior to extraction. Chromatographic peak areas of stable analytes were found to be reproducible (±15%) in field-fortified samples, indicating that no additional error occurred during sample handling under field conditions despite having a less controlled environment. Unstable analytes revealed notable differences in peak areas between fortification times, suggesting that fortification immediately after sample collection is crucial to account for analyte losses during shipping and storage, resulting in accurate quantification of PPCPs. 

ABSTRACT Human polyomaviruses are emerging pathogens that infect a large percentage of the human population and are excreted in urine. Consequently, urine that is collected for fertilizer production often has high concentrations of polyomavirus genes. We studied the fate of infectious double-stranded DNA (dsDNA) BK human polyomavirus (BKPyV) in hydrolyzed source-separated urine with infectivity assays and quantitative PCR (qPCR). Although BKPyV genomes persisted in the hydrolyzed urine for long periods of time ( T 90 [time required for 90% reduction in infectivity or gene copies] of >3 weeks), the viruses were rapidly inactivated ( T 90 of 1.1 to 11 h) in most of the tested urine samples. Interestingly, the infectivity of dsDNA bacteriophage surrogate T3 ( T 90 of 24 to 46 days) was much more persistent than that of BKPyV, highlighting a major shortcoming of using bacteriophages as human virus surrogates. Pasteurization and filtration experiments suggest that BKPyV virus inactivation was due to microorganism activity in the source-separated urine, and SDS-PAGE Western blots showed that BKPyV protein capsid disassembly is concurrent with inactivation. Our results imply that stored urine does not pose a substantial risk of BKPyV transmission, that qPCR and infectivity of the dsDNA surrogate do not accurately depict BKPyV fate, and that microbial inactivation is driven by structural elements of the BKPyV capsid. IMPORTANCE We demonstrate that a common urinary tract virus has a high susceptibility to the conditions in hydrolyzed urine and consequently would not be a substantial exposure route to humans using urine-derived fertilizers. The results have significant implications for understanding virus fate. First, by demonstrating that the dsDNA (double-stranded DNA) genome of the polyomavirus lasts for weeks despite infectivity lasting for hours to days, our work highlights the shortcomings of using qPCR to estimate risks from unculturable viruses. Second, commonly used dsDNA surrogate viruses survived for weeks under the same conditions that BK polyomavirus survived for only hours, highlighting issues with using virus surrogates to predict how human viruses will behave in the environment. Finally, our mechanistic inactivation analysis provides strong evidence that microbial activity drives rapid virus inactivation, likely through capsid disassembly. Overall, our work underlines how subtle structural differences between viruses can greatly impact their environmental fate.