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Fertilizers with additional macronutrients (S, Ca, Mg) may add more numbers to the N-P-K ratio to indicate the amount. The additional numbers are similarly reported in the oxide mass fraction form. For example, a Polish fertilizer labeled "NPK (Ca,S) 4-12-12 (14-29)" has an equivalent of 14% soluble calcium oxide and 29% total sulfur trioxide. [6]
A fertilizer (American English) or fertiliser (British English) is any material of natural or synthetic origin that is applied to soil or to plant tissues to supply plant nutrients. Fertilizers may be distinct from liming materials or other non-nutrient soil amendments. Many sources of fertilizer exist, both natural and industrially produced. [1]
The largest use of monoammonium phosphate by weight is in agriculture, as an ingredient of fertilizers. It supplies soil with the elements nitrogen and phosphorus in a form usable by plants. Its NPK label is 12-61-0 (12-27-0), meaning that it contains 12% by weight of elemental nitrogen and (nominally) 61% of phosphorus pentoxide P 2 O
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When applied as plant fertilizer, it temporarily increases the soil pH, but over a long term the treated ground becomes more acidic than before, upon nitrification of the ammonium. It is incompatible with alkaline chemicals because its ammonium ion is more likely to convert to ammonia in a high-pH environment.
The nitrophosphate process (also known as the Odda process) is a method for the industrial production of nitrogen fertilizers invented by Erling Johnson in the municipality of Odda, Norway around 1927. The process involves acidifying phosphate rock with dilute nitric acid to produce a mixture of phosphoric acid and calcium nitrate.
Fertilizers (ammonium nitrate, urea, NPK fertilizer) and some detergent powders are commonly manufactured as prills. [3] However prilling of ammonium nitrate and urea has in recent years been replaced by fluid bed granulation as this gives strong and more abrasion -resistant granules.
Monopotassium phosphate can exist in several polymorphs.At room temperature it forms paraelectric crystals with tetragonal symmetry. Upon cooling to −150 °C (−238 °F) it transforms to a ferroelectric phase of orthorhombic symmetry, and the transition temperature shifts up to −50 °C (−58 °F) when hydrogen is replaced by deuterium. [8]