Methods and systems for converting ammonium waste streams into certifiably Organic ammonium salts having a variety of uses in greenhouse gas-reducing activities are herein described. The resulting ammonium salt compositions can be used to enhance crop yield.

Methods and systems for converting ammonium waste streams into certifiably Organic ammonium salts having a variety of uses in greenhouse gas-reducing activities are herein described. The resulting ammonium salt compositions can be used to enhance crop yield.

Provided is a novel production system for a product selected from a nitrogen-containing product and a fermented and cultured product that does not involve (or can minimize) the transport of liquid ammonia. A production system for a product selected from a nitrogen-containing product and a fermented and cultured product can include: an ammonia synthesis apparatus in which an ammonia-containing gas is synthesized by reaction of a source gas containing hydrogen and nitrogen in the presence of a supported metal catalyst containing as a support one or more selected from the group consisting of: i) a conductive mayenite compound; ii) a two-dimensional electride compound or a precursor thereof; and iii) a complex formed of a support base containing at least one metal oxide selected from ZrO.sub.2, TiO.sub.2, CeO.sub.2, and MgO and a metal amide represented by a formula M(NH.sub.2).sub.x (where M represents one or more selected from Li, Na, K, Be, Mg, Ca, Sr, Ba, and Eu; and x represents a valence number of M) supported by the support base; and a production apparatus that produces a product selected from a nitrogen-containing product and a fermented and cultured product using ammonia originating from the ammonia-containing gas obtained by using the ammonia synthesis apparatus.

An economical method for recovering phosphate or phosphate and nitrogen from liquid streams. A liquid containing phosphate is introduced into a culture of autotrophic microorganisms in the presence of natural or artificial light, thereby producing a liquid effluent with elevated pH and reduced alkalinity. The alkalinity is reduced through the consumption of bicarbonate/carbonate by the autotrophic microorganisms. The effluent is then chemically treated with low-cost chemicals to provide Ca.sup.++ or Mg.sup.++ ions necessary to form a phosphate precipitate such as calcium phosphate or magnesium-ammonium-phosphate (MAP). The autotrophic microorganisms can be cultivated in ponds, lagoons, or photobioreactors. The pH of the culture is adjustable within a preferred range of 7.5 to 10.5 by adjusting the photobioreactor operation. The process includes an economical flotation separator for solid, liquid, gas separation and a means of concentrating ammonia nitrogen that may also be removed during the process of phosphate reclamation.

An economical method for recovering phosphate or phosphate and nitrogen from liquid streams. A liquid containing phosphate is introduced into a culture of autotrophic microorganisms in the presence of natural or artificial light, thereby producing a liquid effluent with elevated pH and reduced alkalinity. The alkalinity is reduced through the consumption of bicarbonate/carbonate by the autotrophic microorganisms. The effluent is then chemically treated with low-cost chemicals to provide Ca.sup.++ or Mg.sup.++ ions necessary to form a phosphate precipitate such as calcium phosphate or magnesium-ammonium-phosphate (MAP). The autotrophic microorganisms can be cultivated in ponds, lagoons, or photobioreactors. The pH of the culture is adjustable within a preferred range of 7.5 to 10.5 by adjusting the photobioreactor operation. The process includes an economical flotation separator for solid, liquid, gas separation and a means of concentrating ammonia nitrogen that may also be removed during the process of phosphate reclamation.

Provided is a method for detecting impurities in ammonium hydroxide. The method for detecting impurities in ammonium hydroxide includes preparing a potassium permanganate solution, preparing ammonium hydroxide, and adding the potassium permanganate solution several times to the ammonium hydroxide so as to detect impurities in the ammonium hydroxide. Potassium permanganate contained in the potassium permanganate solution is added for each time in the range of 0.0001 mol to 0.01 mol per 1 g of ammonia contained in the ammonium hydroxide.

Provided is a method for detecting impurities in ammonium hydroxide. The method for detecting impurities in ammonium hydroxide includes preparing a potassium permanganate solution, preparing ammonium hydroxide, and adding the potassium permanganate solution several times to the ammonium hydroxide so as to detect impurities in the ammonium hydroxide. Potassium permanganate contained in the potassium permanganate solution is added for each time in the range of 0.0001 mol to 0.01 mol per 1 g of ammonia contained in the ammonium hydroxide.

An ammonia chemical species desorption process desorbs ammonia chemical species adsorbed onto a Prussian blue derivative more simply at lower cost under milder conditions as compared with using an aqueous solution of a salt or strong acid, and only water. This ammonia chemical species desorption process includes an ammonia chemical desorption step of bringing carbon dioxide and water into contact with a Prussian blue derivative represented by the following general formula (1), thereby desorbing an ammonia chemical species.

A.sub.xM[M′(CN).sub.6].sub.y.zH.sub.2O  (1)

where x is 0 to 3, y is 0.1 to 1.5, z is 0 to 6, A is at least one cation of hydrogen, ammonium, an alkaline metal, and an alkaline earth metal, and M and M′ are each independently at least one cation of at least one of atoms having atomic numbers 3 to 83 except for ammonium, an alkali metal, and an alkaline earth metal.

An ammonia chemical species desorption process desorbs ammonia chemical species adsorbed onto a Prussian blue derivative more simply at lower cost under milder conditions as compared with using an aqueous solution of a salt or strong acid, and only water. This ammonia chemical species desorption process includes an ammonia chemical desorption step of bringing carbon dioxide and water into contact with a Prussian blue derivative represented by the following general formula (1), thereby desorbing an ammonia chemical species.

A.sub.xM[M′(CN).sub.6].sub.y.zH.sub.2O  (1)

where x is 0 to 3, y is 0.1 to 1.5, z is 0 to 6, A is at least one cation of hydrogen, ammonium, an alkaline metal, and an alkaline earth metal, and M and M′ are each independently at least one cation of at least one of atoms having atomic numbers 3 to 83 except for ammonium, an alkali metal, and an alkaline earth metal.

The present disclosure is generally directed to a water processing system. In some embodiments, the water processing system may be configured to generate a potassium salt, such as potassium nitrate, an ammonium salt, such as ammonium nitrate, or both. In some embodiments, the water processing system may be at least partially powered by renewable energy, such as by using a liquid storage system that is at least partially underground. In some embodiments, the water processing system may be configured to reuse certain greenhouse emissions to improve performance of power generation systems associated with the water processing system.