Oxidation of Ammonia to Nitrate equation

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donchia
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Oxidation of Ammonia to Nitrate equation

Post by donchia »

Hi guys, can someone please help me with a balanced equation of the oxidation of ammonia to nitrate in water?
Many thanks.
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Post by expert »

There is no such direct method. Ammonia catalytically oxidized by air first to nitric oxide.
NH3 + O2 –> NO + H2O
Nitric oxide simultaneously oxidizes by air to nitric dioxide
NO + O2 –> NO2

Nitric dioxide reacts with water producing nitric acid and nitric oxide:
NO2 + H2O –> HNO3 + NO

Now try to equilibrate each equation. It’s easy.
Remember safety first! Check MSDS and consult with professionals before performing risky experiments.
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Post by AJKOER »

Actually, I just came across a reference in "A dictionary of chemistry and the allied branches of other sciences, Volume 1 By Henry Watts", page 183 (an online Google book) that states NH4OH will react with finely divided Cu (or platinum) in the presence of oxygen or air. One of the byproducts is stated to be "nitride of ammonia". This compound is subsequently given the formula NH4NO2.

Thus, if we can further oxide the NH4NO2 to a nitrate, the mission is accomplished.

However, other than the reference, I have not performed this oxidation myself (although substituting H2O2 for air might be interesting way to speed things up).
Last edited by AJKOER on Fri Apr 15, 2011 11:22 pm, edited 1 time in total.
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Post by expert »

Copper simply oxidizes by air since the oxide is easily soluble in ammonia (blue solution). This refreshes the surface of copper and accelerates further corrosion.
Cu + O2 --> CuO
CuO + 4NH3 (aq) ----> [Cu(NH3)4]2(OH)2

Formation of NH4NO2 in these conditions? I doubt.
Last edited by expert on Sat Apr 16, 2011 10:22 am, edited 1 time in total.
Remember safety first! Check MSDS and consult with professionals before performing risky experiments.
AJKOER
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Post by AJKOER »

I agree, the reference refers to ammonia (aq) which maybe liquid NH3 and not NH4OH.

If it is NH3, then I have just added some catalysts (the platinum catalysts is well know) to your equations. In fact, a platinum catalysts was employed in the first ammonia fueled cars.

A point of confusion (at least for fish owners), is that there are bacteria that can apparently convert NH4+ in a fish tank to nitrate (which kills the fish!).
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Post by expert »

Ammonia (aq) means aqueous ammonia that can be represented as NH4OH. At the same time it’s not ammonia but oxygen that is responsible for corrosion. Ammonia just removes protecting oxide layer and refreshes the surface for further attack. Liquid ammonia is also corrosive to copper
http://www.environmentwriter.org/resour ... mmonia.htm
although I couldn’t find quickly the mechanism. Possibly it’s still air and carbon dioxide that maybe dissolved in liquid ammonia that is a cold or compressed liquid.
Certainly platinum is not something that is related to corrosion. Ammonia driven cars can use liquid ammonia directly as fuel. No platinum required.
http://www.hydrogencarsnow.com/blog2/in ... -vehicles/

In other process platinum may catalyze degradation of ammonia to nitrogen and hydrogen, and hydrogen in turn can be used in hydrogen fuel cells. Degradation of ammonia on platinum is apparently an opposite process to production of ammonia from hydrogen and nitrogen. This is a reversible reaction, so basically it can be used for preservation of hydrogen in a more compact ammonia form:

3 H2 + N2 2 NH3

The downside of liquid ammonia is that it is toxic and suffocating. Also it is a controlled substance, and therefore broad usage may complicate prevention of illegal methamphetamine production.

As for natural production of nitrates from ammonia, yes, this is very common.
http://www.thetropicaltank.co.uk/cycling2.htm
http://en.wikipedia.org/wiki/Nitrogen_cycle
Remember safety first! Check MSDS and consult with professionals before performing risky experiments.
AJKOER
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Post by AJKOER »

Per http://en.wikipedia.org/wiki/Ammonia
"The combustion of ammonia in air is very difficult in the absence of a catalyst (such as platinum gauze), as the temperature of the flame is usually lower than the ignition temperature of the ammonia-air mixture." Thus, my comments on the first ammonia engine is valid.

Also, the combustion of ammonia produces nitrogen and water and not nitrogen oxides unless supported by catalyst.

4 NH3 + 3 O2 → 2 N2 + 6 H2O

Per the same source, "However, nitrogen oxides can be formed as kinetic products in the presence of appropriate catalysts, a reaction of great industrial importance in the production of nitric acid:"

4 NH3 + 5 O2 → 4 NO + 6 H2O
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Post by expert »

You are right about the reactions: ammonia burns nicely without catalysts (green flame) into N2 and H2O. In the presence of platinum it can oxidize into NO.
Again, no need for a catalist to burn ammonia on air.
Remember safety first! Check MSDS and consult with professionals before performing risky experiments.
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Post by AJKOER »

The link below is a 2008 article on the oxidation of NH3 with O2 in the presence of a Bimetallic CuO/CeO2 Nanoparticle Catalyst authored by Chang-Mao Hung, Taiwan, Republic of China:

http://www.aaqr.org/VOL8_No4_December20 ... 47-458.pdf

To quote "The catalytic oxidation of ammonia has been reported to precede as follows the exothermic global reactions:

4NH3 + 3O2 → 2N2 + 6H2O +1266 KJ (1)
2NH3 + 2O2 → N2O + 3H2O +1102 KJ (2)
4NH3 + 5O2 → 4NO + 6H2O +904 KJ (3)

The SCO process that involves ammonia should be selective for nitrogen (reaction 1), and prevent further oxidation of nitrogen (reactions 2 and 3)"

What I find fascinating is how the original reference in Watt's Dictionary of Chemistry, over a century old, has been updated from the oxidation of ammonia in the presence of "finely divided copper" to a bimetallic CuO/CeO2 nanoparticle catalyst.

On the discussion as to whether the ammonia reference in Watt's is NH3 or NH4OH, there are some recent papers citing wet oxidation of ammonia, so the point appears to be mute. For example, the link below brings up a pdf dated April 2010 entitled "CATALYTIC WET AIR OXIDATION OF AQUEOUS SOLUTIONS OF AMMONIA IN A CONTINUOUS-FLOW TRICKLE-BED REACTOR OVER METAL SUPPORTED ON CARBON MATERIALS" by Chang-Mao Hung1,* and Wei-Bang Lin2

The metal referred to is Cu-activated carbon fiber (ACF) catalyst.

http://doc-0o-a0-docsviewer.googleuserc ... ci4fq4tm7j
ajkoer
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Post by expert »

Your link doesn't work. Maybe this?
http://www.ncbi.nlm.nih.gov/pubmed/19147285

I recommend using this site http://tinyurl.com/ to abbreviate your long links
Remember safety first! Check MSDS and consult with professionals before performing risky experiments.
AJKOER
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Post by AJKOER »

OK, I just came across a series of papers in the processing of waste water. It turns out that my earlier idea of replacing the use of oxygen with a stronger oxiderizer was on track. See for example, the paper by Karlis Svanks, "Oxidation of Ammonia in Water by Ferrates(VI) and (IV)"
https://kb.osu.edu/dspace/bitstream/han ... sequence=1 .

My guess is that the general goal in waste managment is the efficient and economical removal of NH3 by oxidation in a normal temperature band and, on occasion, the restoration of nitrates. It terms out that Ferrates are perhaps the strongest oxidizes around yielding mono-atomic oxygen and are capable of oxidizing NH4OH at room temperature. One equation given by Svanks, with excess K2FeO4, for example, directly produces a nitrate:

8 K2FeO4 + 3 NH3 + (n+2)H2O --> 3 KNO3 + 4 Fe2O3.nH2O + 13 KOH

Another reference gives the optimal Ph between 7.5 to 11 and the temperature between 10C to 35C to produce nitrates.

The main issue is how to prepare K2FeO4 as it not commercially available and has a shelf life of about 8 - 9 hours. One cited method is as follow:

2Fe(NO3)3 + 3NaOCl + 10NaOH ->2Na2FeO4 + 5H2O + 3NaCl + 6NaNO3

Unfortunatley, the yield is low around 10-15%. However, replacing Na2(FeO4) with the insoluble Barium Ferrate is said to increase ferrate production. The use of Ferric Nitrate seems to be preferable over Ferric Chloride and Fe(OH)3. The web and above work by Svanks give other possible ferrate preparations with better yields. There is a recent Iranian Chemical Society paper detailing improvements resulting in higher yields to the Ferric Nitrate approach. Link is:
http://www.ics-ir.org/jics/archive/v7/4 ... icle-3.pdf

Interestingly, the use of ferrates to oxide ammonia does not require a high temperature, an elevated pressure or even a catalyst. For laboratory preparations, I wouild speculate that a CuO catalyst may increase the rate of ammonia conversion.
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