Soil Property Effect on Nitrogen Mineralization of Dairy Manure in the Pacific Northwest

Purpose

Growers often use total nitrogen (N) concentration of dairy manure to estimate plant available N for crop production. This estimate often does not take into account the role soil properties may have on N mineralization (Nmin) rates. This study aims to determine how soil properties impact Nmin rates of dairy manure and composted dairy manure by aerobic incubation. The soil properties investigated, including soil texture, percent organic matter, pH, EC, buffer pH, NO3-N, NH4-N, Olsen P, K, Ca, Mg, Na, CEC, S, Zn, Fe, Mn, Cu, B, and CaCO3 equivalent, which are all accessible to producers sending soil samples to a commercial soil laboratory. The goal of this project is to incorporate soil properties into N availability prediction models for dairy manure to improve N use efficiency of field-applied manure.

What Did We Do?

A total of 16 different soil series were sampled throughout Oregon, Washington, and Idaho in major dairy producing counties at a 12-inch depth. These soils represent over 1.6 million acres in the Pacific Northwest (PNW). One solid dairy manure was sampled in Idaho and one composted dairy manure was sampled in Oregon to be applied to the soils during incubation. All the soils were analyzed for a full suite of soil physiochemical properties at a local soil testing laboratory. The manures similarly received a full analysis at the same laboratory.

We conducted a 12-week incubation of manure-amended soils at 77°F (25°C), sampling periodically for nitrate and ammonium to determine the difference in Nmin rates with changes in soil physiochemical properties. Approximately 1.1 lbs (500 g) of soil was added to 1-gallon Ziplock bags and brought to 80% field capacity. The soils were treated with dairy manure, composted manure, or no manure at a rate of approximately 400 lb N/acre (200 mg N/kg soil) with four replicates for each soil and treatment. Each of the 192 samples were randomly assigned a sample number corresponding to their location inside the incubator. The closed and loosely rolled bags were stored in 12 by 9 by 7-inch cardboard boxes, then placed inside an incubator at 77°F for 12 weeks. Soils were sampled at weeks 0, 2, 4, 8, and 12, where part of the sample was used to monitor soil moisture, and the other was frozen for future analysis. Analysis of the frozen samples for nitrate and ammonium content was conducted using a microplate spectrophotometer using vanadium (III) chloride and sodium salicylate methods, respectively.

What Have We Learned?

The analysis of frozen samples has just begun at the time of submission. Initial results will be available on the poster presented.

Future Plans

The next steps of this project are to conclude the nitrate and ammonium analysis of the soil samples and create Nmin curves with this data for each soil and treatment. These curves will be analyzed to determine if the differences in Nmin rates correlate with any of the tested soil physiochemical properties and which properties are most influential. Finally, we will create a model based on correlation data to express the changes in nitrogen mineralization depending on soil physiochemical properties that can be used by producers to adjust their dairy manure application rates depending on their soil test results.

Authors

Presenting author

Ryan A. Auld, Soil Science Graduate Student, Oregon State University

Corresponding author

Amber Moore, Extension Soil Fertility Specialist, Oregon State University, Amber.moore@oregonstate.edu

Additional authors

Jennifer Moore, Research Soil Scientist, Forage Seed and Cereal Research Unit, U.S. Department of Agriculture Agricultural Research Service; Yakun Zhang, Associate Professor, Oregon State University; Christopher Rogers, Research Soil Scientist, Northwest Irrigation and Soils Research, U.S. Department of Agriculture Agricultural Research Service

Additional Information

Build DAIRY

Acknowledgements

I’d like to acknowledge the BUILD Dairy program and the Oregon Dairy Farmers Association for their support of this project, as well as the many producers who have allowed me to sample soils from their farms.

The authors are solely responsible for the content of these proceedings. The technical information does not necessarily reflect the official position of the sponsoring agencies or institutions represented by planning committee members, and inclusion and distribution herein does not constitute an endorsement of views expressed by the same. Printed materials included herein are not refereed publications. Citations should appear as follows. EXAMPLE: Authors. 2025. Title of presentation. Waste to Worth. Boise, ID. April 711, 2025. URL of this page. Accessed on: today’s date.

Advances in Nutrient Recovery Technology: Approaches to Controlling Recovered Product Chemistry

Purpose

Our recent work has focused on developing approaches to nutrient management and recovery, with a particular focus on using electrochemical and membrane technologies to control the chemistry of the recovered nutrient products. We are interested in being able to recover both ammonia and phosphate, and our goal is to create recycled fertilizer products that can allow the agricultural community to control the ratio of nitrogen to phosphorus in the recycled fertilizer products and to control whether those fertilizer products are in liquid form or in solid form. With the electrochemical technology focus, we see benefits that include no required chemical dosing, scalable reactor design, and the ability to couple to renewable energy sources. Our engineering research on nutrient recovery technology is conducted within a team that includes life cycle assessment, economic analysis, agronomic greenhouse and row crop studies, agricultural sector outreach, and the development of a decision-support tool to help farmers understand technology options for water and nutrient management.

What Did We Do?

We have investigated an electrochemical cell design that includes a magnesium metal anode and a stainless-steel cathode. The corrosion of the magnesium anode results in the release of magnesium cations into solution, and these magnesium cations promote the precipitation of struvite, otherwise known as magnesium ammonium phosphate hexahydrate (Figure 1). We have investigated how operating conditions of the electrochemical cell, including voltage, residence time, batch vs flow, and membrane separation of the two electrodes, affect nutrient recovery efficiency and the overall chemistry of the recovered precipitate. Our studies have included control experiments on synthetic wastewater compositions relevant to hog and dairy farm wastewaters, while we have also conducted laboratory-scale studies on natural wastewater samples from both agricultural and municipal sources. To demonstrate initial scale-up of an electrochemical reactor, we have designed a bench-scale reactor (Figure 2) that is capable of producing kilogram-level batches of struvite.

Figure 2. (a) Bench-scale batch reactor demonstration for kg-level struvite precipitation. (b) One engineering challenge is the precipitation of struvite on the electrode surface.

What Have We Learned?

The production of struvite from an electrochemical reactor can be controlled by the applied voltage and residence time of the wastewater in the reactor. Changes in reactor design, including the inclusion of a membrane to separate the anode and cathode and operation in batch vs flow mode, can change the composition of the struvite precipitate and can cause a change in the balance of struvite formed vs hydrogen gas formed from the electrochemical cell. We are also able to produce K-struvite, a potassium-based alternative to conventional struvite, that includes potassium rather than ammonium, and the production of K-struvite allows the recovery of the phosphate in a particulate fertilizer while also allowing the separation and recovery of ammonia in a separate liquid stream. We have learned that one of the primary challenges to the electrochemical reactor operation is fouling of the electrodes by the struvite precipitate (Figure 2), and we have developed a dynamic voltage control approach that enables minimal electrode fouling and therefore increases struvite recovery and decreases energy consumption. Our energy consumption values are similar to that of chemical precipitation processes that have been developed for nutrient recovery.

Future Plans

Future plans include further development and optimization of the dynamic voltage control approach to electrochemical reactor operation, which will allow us to control electrode fouling. We also plan to continue working with natural wastewater samples and further develop flow cell reactor design to understand how to translate our batch reactor studies to a flow reactor environment. Studies on K-struvite will focus on understanding the kinetics of K-struvite precipitation and the competing reactions (e.g., calcium precipitation and struvite precipitation) that might impact K-struvite recovery.

Authors

Lauren F. Greenlee, Associate Professor, Pennsylvania State University

Corresponding author email address

greenlee@psu.edu

Additional authors

Laszlo Kekedy-Nagy, Postdoctoral Fellow, Concordia University

Ruhi Sultana, Graduate Research Assistant, Pennsylvania State University

Amir Akbari, Graduate Research Assistant, Pennsylvania State University

Ivy Wu, Graduate Research Assistant, Colorado School of Mines

Andrew Herring, Professor, Colorado School of Mines

Additional Information

    1. Kekedy-Nagy, Z. Anari, M. Abolhassani, B.G. Pollet, L.F. Greenlee. Electrochemical Nutrient Removal from Natural Wastewater Sources and its Impact on Water Quality. Water Research (2022), 210, 118001, DOI: 10.1016/j.watres.2021.118001.
    2. Kékedy-Nagy, M. Abolhassani, R. Sultana, Z. Anari, K.R. Brye, B.G. Pollet, L. F. Greenlee. The Effect of Anode Degradation on Energy Demand and Production Efficiency of Electrochemically Precipitated Struvite, Journal of Applied Electrochemistry (2021), DOI: 0.1007/s10800-021-01637-y.
    3. Kékedy-Nagy, M. Abolhassani, S.I. Perez Bakovic, J.P. Moore II, B.G. Pollet, L.F. Greenlee. Electroless Production of Fertilizer (Struvite) and Hydrogen from Synthetic Agricultural Wastewaters, Journal of the American Chemical Society (2020), 142(44), 18844-18858. DOI: /10.1021/jacs.0c07916.
    4. Wu, A. Teymouri, R. Park, L.F. Greenlee, and A.M. Herring. Simultaneous Electrochemical Nutrient Recovery and Hydrogen Generation from Model Wastewater Using a Sacrificial Magnesium Anode, Journal of the Electrochemical Society (2019), 166(16), E576-E583. DOI: 10.1149/2.0561916jes.

Acknowledgements

The authors acknowledge funding from the USDA NIFA AFRI Water for Food Production Systems program, grant #2018-68011-28691 and funding from the National Science Foundation, grant #1739473.

 

The authors are solely responsible for the content of these proceedings. The technical information does not necessarily reflect the official position of the sponsoring agencies or institutions represented by planning committee members, and inclusion and distribution herein does not constitute an endorsement of views expressed by the same. Printed materials included herein are not refereed publications. Citations should appear as follows. EXAMPLE: Authors. 2022. Title of presentation. Waste to Worth. Oregon, OH. April 18-22, 2022. URL of this page. Accessed on: today’s date.