SULFAMIC ACID
Chemical Formula: HSO3NH2
CAS Number: 5329-14-6
Molecular Weight: 97.10
Equivalent Weight: 97.10
Density at 25
oC: 2.126 g/cm3
Specific
heat: 1.1467
J/g
Melting
point: 205
oC
Decomposition
Temperature: 209◦C
Vapor
pressure:
20 oC
0.8 Pa
100 oC 0.25 Pa
Sulfamic acid has a unique and
important combination of properties. Sulfamic acid is a white or colorless,
odorless, crystalline (sand like), nonhygroscopic, dry, strong inorganic acid.
At room temperature it is non-volatile. Therefore it is conveniently handled
and packaged in solid form in bags and is easily transported commercially. It
is highly stable and can be stored for years without change in properties.
Sulfamic Acid is monoamide of sulphuric acid.
Alternatively it is also known as
amidosulfonic acid, amidosulfuric acid (IUPAC recommended), aminosulfonic
acid, sulphamic acid.
Pure Sulfamic Acid melts at 205 oC
and starts decomposing at 209 oC. On decomposition Sulfur trioxide,
sulfur dioxide, water, ammonia, and nitrogen are evolved.
Aqueous Sulfamic Acid solutions are
practically stable at room temperature but hydrolyze exothermically to ammonium
hydrogen sulfate at high temeratures :
NH2SO3H+H2O → NH4HSO4
Rate of hydrolysis increases with the increase of
concentration and temperature and at lower pH.
Sulfamic Acid reacts with metals,
alkali and alkaline earth metals and their oxides, hydroxides and carbonates
and forms metal sulfamates. These metal sulfamates are, with but few
exceptions, soluble in water. The sulfamates of lead, magnesium, and sodium are
more soluble in water than the corresponding sulfates, nitrates, chlorides, and
acetates. Therefore it is used in cleaning and descaling operations. Its
corrosiveness towards metals can be controlled by adding corrosion inhibitors.
Metal sulfamate solutions are stable at high temperatures and can be evaporated
to dryness on a steam bath without hydrolysis of the amide group. Acidic metal
oxides react with sulfamic acid less readily or not at all.
Nitrites react rapidly with
sulfamic acid, liberating nitrogen and forming sulfuric acid. This reaction is
utilized for the analytical determination of nitrites or of sulfamic acid even
in the presence of nitrates.
Sulfamic Acid reacts with primary
alcohols, glycols and glycerine upon heating and form corresponding esters.
Sulfamic acid is highly ionized in
aqueous solution, and its pH range approaches that of nitric, sulfuric, and
hydrochloric acids.
At low temperatures chlorine,
bromine, and chlorates oxidize sulfamic acid to sulfuric acid. Potassium
permanganate, chromic acid, and ferric chloride do not oxidize sulfamic acid.
Sulfamic acid reacts with
concentrated nitric acid to form nitrous oxide:
NH2SO2OH
+ HNO3 → H2SO4+
H2O+N2O
This reaction is used as a convenient method
for preparing pure nitrous oxide.
Sulfamic Acid is fairly soluble in
water and nitrogenous
solvents such as liquid ammonia formamide, slightly soluble in methanol, and
insoluble in ethanol, acetone, and ether. Sulfamic acid is insoluble in organic oxygen-containing and
most nonpolar organic solvents, hydrocarbons, chlorinated hydrocarbons, carbon
disulfide, toluene and sulfur dioxide. The solubility of sulfamic acid in water
is decreased markedly by sulfuric acid and sodium sulfate. Sulfamic acid is practically insoluble
in 70-100% sulfuric acid. Its solubility in Fuming Sulfuric Acid (21% SO3) is 2.38 gram in 100
grams of acid.
Solubility of Sulfamic Acid in
water:
Temperature oC
|
Solubility
per 100 gram water
|
Temperature oC
|
Solubility
per 100 gram water
|
0
|
14.68
grams
|
50
|
32.82
grams
|
10
|
18.56
grams
|
60
|
37.10
grams
|
20
|
21.32
grams
|
70
|
41.91
grams
|
30
|
26.09
grams
|
80
|
47.08
grams
|
40
|
29.49
grams
|
Solubility of Sulfamic Acid in
Organic solvents at 25 oC per 100 grams of solvent:
Methanol 4.3 gram
Ethanol 1.7 gram
Acetone 0.4 gram
Ether 0.009 gram
Formamide 20.0 gram
pH of Sulfamic Acid solutions in
water at 25 oC are :
5% 0.63
2.5% 0.86
1% 1.18
0.5% 1.41
Upon brief contact with the skin
sulfamic acid shows no noticeable effect but, as a normal safety precaution, it is recommended that
prolonged exposures be avoided. Similarly, in two hundred human test cases, fabric
treated with ammonium sulfamate produced no skin irritation.
In 1936 a practical process, which
became the basis for commercial preparation was developed. In this production process, urea is first dissolved in excess
cold sulfuric acid. Oleum of suitable sulfur trioxide strength is then added,
and the reaction is allowed to proceed under controlled conditions. During the
reaction carbon dioxide is evolved, and the sulfamic acid formed precipitates
from the solution. The product is isolated by filtration and purified by recrystallization
from water. This process involving urea with sulphur trioxide and sulphuric
acid continues to be the main method for production of sulphamic acid today.