Search for: All records

Abstract Struvite (MgNH₄PO₄·6H₂O) has been precipitated from liquid waste streams to recover valuable nutrients, such as phosphorus (P) and nitrogen (N), that can be used as an alternative fertilizer‐P source. Because prior research has focused on greenhouse studies, it is necessary to expand struvite evaluations to the field‐scale to include row‐crop responses. The objective of this field study was to evaluate the effects of two struvite materials (electrochemically precipitated struvite, ECST; and chemically precipitated struvite, CPST) relative to other common fertilizer‐P sources (diammonium phosphate, DAP; triple superphosphate, TSP; rock phosphate, RP; and monoammonium phosphate, MAP) on soybean [Glycine max(L.) Merr.] response and economics in two consecutive growing seasons in a P‐deficient, silt‐loam soil (Aquic Fraglossudalfs) in eastern Arkansas. Averaged across years, soybean aboveground tissue P uptake was largest (P < .05) from ECST (28.4 kg ha⁻¹), which was similar to CPST (26.7 kg ha⁻¹) and TSP (25.9 kg ha⁻¹) and was smallest from RP (21.4 kg ha⁻¹). In 2019, seed yield was largest (P < .05) from ECST (4.1 Mg ha⁻¹), which was similar to DAP, CPST, RP, TSP, and MAP, and was smallest from the unamended control (3.6 Mg ha⁻¹). In 2020, seed yield was numerically greatest from CPST (2.8 Mg ha⁻¹) and was numerically smallest from ECST (2.2 Mg ha⁻¹). Results showed that wastewater‐recovered struvite materials have the potential to be a viable, alternative fertilizer‐P source for soybean production in a P‐deficient, silt‐loam soil, but further work is needed to confirm struvite's cost effectiveness. 

Abstract Cerium has a wide range of current and emerging applications, and the binding of cerium ions to solid substrates is important for cerium recovery, or in advanced material synthesis. In this study, we investigate the affinity of a surface‐bound peptide derived from the EF‐hand loop I of calmodulin for cerium (III) ions and compare the results to a scrambled control. Results obtained via quartz crystal microbalance with dissipation are used to estimate the dissociation constant between the bound EF‐hand loop I peptide and cerium (III) ions (1.3 ± 0.1 μM), which is comparable with other dissociation constants measured for EF‐hand peptides and cerium ions in solution reported this work and in literature (0.95‐5.8 μM). Circular dichroism also suggests that the peptide binds to cerium (III) ions in solution, and undergoes a secondary structural change upon binding. Overall, this study shows that EF‐hand loop peptides are capable of binding cerium (III) ions in solution and when attached to a solid substrate. 

Rare earth elements (REEs) are a vital part of many technologies with particular importance to the renewable energy sector and there is a pressing need for environmentally friendly and sustainable processes to recover and recycle them from waste streams. Functionalized polymer scaffolds are a promising means to recover REEs due to the ability to engineer both transport properties of the porous material and specificity for target ions. In this work, REE adsorbing polymer scaffolds were synthesized by first introducing poly(glycidyl methacrylate) (GMA) brushes onto porous polyvinylidene fluoride (PVDF) surface through activator generated electron transfer atom transfer radical polymerization (AGET ATRP). Azide moieties were then introduced through a ring opening reaction of GMA. Subsequently, REE-binding peptides were conjugated to the polymer surface through copper catalyzed azide alkyne cycloaddition (CuAAC) click chemistry. The presence of GMA, azide, and peptide was confirmed through Fourier transform infrared spectroscopy. Polymer scaffolds functionalized with the REE-binding peptide bound cerium, while polymer scaffolds functionalized with a scrambled control peptide bound significantly less cerium. Importantly, this study shows that the REE binding peptide retains its functionality when bound to a polymer surface. The conjugation strategy employed in this work can be used to introduce peptides onto other polymeric surfaces and tailor surface specificity for a wide variety of ions and small molecules. 

Nutrient recovery in domestic wastewater treatment has increasingly become an important area of study as the supply of non-renewable phosphorus decreases. Recent bench-scale trials indicate that co-generation of struvite and hydrogen using electrochemical methods may offer an alternative to existing recovery options utilized by municipal wastewater treatment facilities. However, implementation has yet to be explored at plant-scale. In the development of novel nutrient recovery processes, both economic and environmental assessments are necessary to guide research and their design. The aim of this study was to conduct a prospective life cycle assessment and cost analysis of a new electrochemical struvite recovery technology that utilizes a sacrificial magnesium anode to precipitate struvite and generate hydrogen gas. This technology was modeled using process simulation software GPS-X and CapdetWorks assuming its integration in a full-scale existing wastewater treatment plant with and without anaerobic digestion. Struvite recoveries of 18–33% were achieved when anaerobic digestion was included, with a break-even price of $6.03/kg struvite and $15.58/kg of hydrogen required to offset increased costs for recovery. Struvite recovery reduced aquatic eutrophication impacts as well as terrestrial acidification impacts. Tradeoffs between benefits from struvite and burdens from electrode manufacturing were found for several impact categories. 

Phosphorus (P) recovery from wastewaters as struvite (MgNH4PO4·6H2O) may be a viable alternative fertilizer-P source for agriculture. The objective of this study was to evaluate the economic and environmental implications of struvite as a fertilizer-P source for flood-irrigated rice (Oryza sativa) relative to other commonly used commercially available fertilizer-P sources. A field study was conducted in 2019 and 2020 to evaluate the effects of wastewater-recovered struvite (chemically precipitated struvite (CPST) and electrochemically precipitated struvite (ECST)) on rice yield response in a P-deficient, silt–loam soil in eastern Arkansas relative to triple superphosphate, monoammonium and diammonium phosphate, and rock phosphate. A life cycle assessment methodology was used to estimate the global warming potentials associated with rice produced with the various fertilizer-P sources. Life cycle inventory data were based on the field trials conducted with and without struvite application for both years. A partial budget analysis showed that, across both years, net revenues for ECST and CPST were 1.4 to 26.8% lower than those associated with the other fertilizer-P sources. The estimated greenhouse gas emissions varied between 0.58 and 0.70 kg CO2 eq kg rice−1 from CPST and between 0.56 and 0.81 kg CO2 eq kg rice−1 from ECST in 2019 and 2020, respectively, which were numerically similar to those for the other fertilizer-P sources in 2019 and 2020. The similar rice responses compared to commercially available fertilizer-P sources suggest that wastewater-recovered struvite materials might be an alternative fertilizer-P-source option for flood-irrigated rice production if struvite can become price-competitive to other fertilizer-P sources. 

The perception of wastewater as a resource rather than a pollutant has not been well emphasized. Phosphorus (P) can be precipitated from wastewaters as the mineral struvite (MgNH4PO4·6H2O), which can be a potential sustainable alternative to the limited, rock phosphate (RP)-dependent, traditional fertilizer-P sources for agricultural production. This field study evaluated the effects of electrochemically precipitated struvite (ECST) and chemically precipitated struvite (CPST) compared to other conventional fertilizer-P materials [monoammonium phosphate (MAP), diammonium phosphate (DAP), triple superphosphate (TSP), and RP] on corn (Zea mays L.) response in two consecutive growing seasons in a P-deficient, silt-loam soil (Aquic Fraglossudalfs) in eastern Arkansas. Averaged across years, corn yield was numerically largest from ECST (12.9 Mg ha–1), which differed (P < 0.05) from all other treatments and was numerically smallest from DAP (10.1 Mg ha–1), which was similar to MAP (10.7 Mg ha–1), CPST (10.3 Mg ha–1), and RP (10.3 Mg ha–1). Corn yield and kernel P uptake from ECST were at least 1.2 times greater (P < 0.05) than from CPST, TSP, DAP, and RP. Yield from ECST was 1.2 times greater (P < 0.05) than from MAP. A partial budget analysis showed that, across both years, fertilizer-P treatment net revenues for ECST were greater than those associated with the other fertilizer-P sources. Results demonstrated that wastewater-recovered struvite materials have the potential to be a sustainable source of P for corn production in P-deficient, silt-loam soil from both a technical and economic perspective.