Hydrogen Sulfide

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Hydrogen sulfide

Hydrogen sulfide is a chemical compound


with the formula H2S. It is a colorless
chalcogen-hydride gas, and is poisonous,
corrosive, and flammable, with trace
amounts in ambient atmosphere having a
characteristic foul odor of rotten eggs.[11]
The underground mine gas term for foul-
smelling hydrogen sulfide-rich gas
mixtures is stinkdamp. Swedish chemist
Carl Wilhelm Scheele is credited with
having discovered the chemical
composition of purified hydrogen sulfide in
1777.[12]

Hydrogen sulfide is toxic to humans and


most other animals by inhibiting cellular
respiration in a manner similar to hydrogen
cyanide. When it is inhaled or its salts are
ingested in high amounts, damage to
organs occurs rapidly with symptoms
ranging from breathing difficulties to
convulsions and death.[13][14] Despite this,
the human body produces small amounts
of this sulfide and its mineral salts, and
uses it as a signalling molecule.[15]
Hydrogen sulfide is
Hydrogen sulfide
often produced
from the microbial
breakdown of
organic matter in
the absence of
Sulfur,
oxygen, such as in
S
swamps and
sewers; this process
Hydrogen,
is commonly known
H
as anaerobic
digestion, which is Names
done by sulfate-
Systematic IUPAC
reducing name
microorganisms. It Hydrogen
sulfide[1]
also occurs in
volcanic gases, Other names
natural gas Dihydrogen
deposits, and monosulfide

sometimes in well- Sour gas


Dihydrogen
drawn water.
sulfide
Properties Sewer gas
Egg gas
Hydrogen sulfide is
Sulfane
slightly denser than Sulfurated
air. A mixture of H2S hydrogen
and air can be Sulfureted
explosive. In hydrogen
general, hydrogen Sulfuretted

sulfide acts as a hydrogen


Sulfur hydride
reducing agent,
although in the
presence of a base, Hydrosulfuric
it can act as an acid acid

by donating a proton Hydrothionic


− acid
and forming SH .
Thiohydroxic
Hydrogen sulfide acid
Sulfhydric acid
burns in oxygen with
a blue flame to form Identifiers

sulfur dioxide (SO2) CAS 7783-06-


Number
and water: 4 (http
s://com
monche
mistry.ca
s.org/det
ail?cas_r
n=7783-0
6-4)
3D Interactive
model
image (htt
(JSmol)
ps://chem
apps.stola
f.edu/jmo
l/jmol.ph
p?model=
S)

3DMet B01206
(http://w
ww.3dm
et.dna.af
frc.go.jp/
cgi/show
_data.ph
p?acc=B
01206)
Beilstein 3535004
Reference

ChEBI CHEBI:16136
(https://ww
w.ebi.ac.uk/c
hebi/searchI
d.do?chebiId
=16136)

ChEMBL ChEMBL120
0739 (http
s://www.eb
ac.uk/chem
ldb/index.p
p/compoun
d/inspect/C
EMBL12007
39)
ChemSpi 391 (http
der s://www.
chemspi
der.com/
Chemical
-Structur
e.391.ht
ml)

ECHA 100.029.07
InfoCard (https://ech
a.europa.e
u/substanc
-informatio
n/-/substan
ceinfo/100.
029.070)
EC 231-977-
Number 3

Gmelin 303
Reference

KEGG C00283
(https://
www.keg
g.jp/entr
y/C0028
3)

MeSH Hydrogen+s
ulfide (http
s://www.nlm.
nih.gov/cgi/
mesh/2014/
MB_cgi?mod
e=&term=Hy
drogen+sulfi
de)

PubChem 402 (http


CID
s://pubch
em.ncbi.
nlm.nih.g
ov/comp
ound/40
2)

RTECS MX1225000
number

UNII YY9FVM7NS
N (https://pr
ecision.fda.g
ov/uniisearc
h/srs/unii/Y
Y9FVM7NS
N)

UN 1053
number

CompTox DTXSID402
Dashboard
149 (https:/
(EPA)
comptox.ep
a.gov/dash
oard/chem
al/details/D
XSID40241
9)

InChI
InChI=1S/H2S/h1
H2
Key: RWSOTUBLDI
XVET-UHFFFA
OYSA-N
InChI=1/H2S/h1H
2
Key: RWSOTUBLDI
XVET-UHFFFA
OYAJ

SMILES
S

Properties

Chemical H2S
formula

Molar 34.08 g·mol−


mass 1

Appeara Colorless
nce gas

Odor Foul,
pungent,
like that
of rotten
eggs

Density 1.539
g.L−1
(0°C)[2]

Melting −85.5[3] °C
point (−121.9 °F;
187.7 K)

Boiling −59.55[3] °C
point (−75.19 °F;
213.60 K)

Solubility 3.980 g
in water
dm−3 (at
20 °C) [4]

Vapor 1740 kPa


pressure (at 21 °C)
Acidity 7.0[5][6]
(pKa)

Conjuga Sulfonium
te acid

Conjugat Bisulfide
e base

Magnetic −25.5·10−6
susceptibility 3
cm /mol
(χ)

Refractive 1.000644
index (nD)
(0 °C)[2]

Structure

Point C2v
group

Molecular Bent
shape
Dipole 0.97 D
moment

Thermochemistry

Heat 1.003 J
capacity
K−1 g−1
(C )
Std 206 J
molar
mol−1
entropy
(S⦵298) K−1[7]

Std −21 kJ
enthalpy
mol−1[7]
of
formation
(ΔfH⦵298)
Hazards

Occupational safety
and health
(OHS/OSH):

Main Flammable
hazards
and highly
toxic

GHS labelling:

Pictograms

Signal Danger
word

Hazard H220,
statements
H330,
H400

Precautionary
P210, P26
statements
P271, P27
P284,
P304+P34
P310, P32
P377, P38
P391, P40
P403+P23
P405, P50

NFPA 4
4
0

704
(fire dia
mond)

Flash −82.4 °C
point (−116.3 °F;
190.8 K)[10]

Autoignition232 °C
temperature
(450 °F;
505 K)
Explosive 4.3–46%
limits

Lethal dose or
concentration (LD,
LC):

LC50 (median
713
concentration)
ppm
(rat, 1
hr)
673
ppm
(mouse,
1 hr)
634
ppm
(mouse,
1 hr)
444
ppm
(rat, 4
hr)[9]

LCLo 600
(lowest ppm
published)
(human,
30 min)
800
ppm
(human,
5 min)[9]

NIOSH (US health


exposure limits):

PEL C 20
(Permissible)
ppm; 50
ppm [10-
minute
maximum
peak][8]

REL C 10 ppm
(Recommended)
(15 mg/m
[10-
minute][8]

IDLH 100
(Immediate [8]
ppm
danger)

Related compounds

Related Water
hydrogen
Hydrogen
chalcogenides
selenide
Hydrogen
telluride
Hydrogen
polonide
Hydrogen
disulfide
Sulfanyl

Related Phosphine
compounds

Except where
otherwise noted,
data are given for
materials in their
standard state (at
25 °C [77 °F],
100 kPa).
verify (https://en.w
ikipedia.org/w/inde
x.php?title=Special:
ComparePages&rev
1=477313464&page
2=Hydrogen+sulfid
e) (what is ?)
Infobox references

2 H2S + 3 O2 → 2 SO2 + 2 H2O

If an excess of oxygen is present, sulfur


trioxide (SO3) is formed, which quickly
hydrates to sulfuric acid:

H2S + 2 O2 → H2SO4

At high temperatures or in the presence of


catalysts, sulfur dioxide reacts with
hydrogen sulfide to form elemental sulfur
and water. This reaction is exploited in the
Claus process, an important industrial
method to dispose of hydrogen sulfide.
Hydrogen sulfide is slightly soluble in
water and acts as a weak acid (pKa = 6.9
in 0.01–0.1 mol/litre solutions at 18 °C),

giving the hydrosulfide ion HS (also

written SH ). Hydrogen sulfide and its
solutions are colorless. When exposed to
air, it slowly oxidizes to form elemental
sulfur, which is not soluble in water. The
sulfide anion S2− is not formed in aqueous
solution.[16]

Hydrogen sulfide reacts with metal ions to


form metal sulfides, which are insoluble,
often dark colored solids. Lead(II) acetate
paper is used to detect hydrogen sulfide
because it readily converts to lead(II)
sulfide, which is black. Treating metal
sulfides with strong acid or electrolysis
often liberates hydrogen sulfide. Hydrogen
sulfide is also responsible for tarnishing
on various metals including copper and
silver; the chemical responsible for black
toning found on silver coins is silver
sulfide (Ag2S), which is produced when the
silver on the surface of the coin reacts
with atmospheric hydrogen sulfide.[17]

At pressures above 90 GPa (gigapascal),


hydrogen sulfide becomes a metallic
conductor of electricity. When cooled
below a critical temperature this high-
pressure phase exhibits superconductivity.
The critical temperature increases with
pressure, ranging from 23 K at 100 GPa to
150 K at 200 GPa.[18] If hydrogen sulfide is
pressurized at higher temperatures, then
cooled, the critical temperature reaches
203 K (−70 °C), the highest accepted
superconducting critical temperature as of
2015. By substituting a small part of sulfur
with phosphorus and using even higher
pressures, it has been predicted that it
may be possible to raise the critical
temperature to above 0 °C (273 K) and
achieve room-temperature
superconductivity.[19]
Hydrogen sulfide decomposes without a
presence of a catalyst under atmospheric
pressure around 1200 °C into hydrogen
and sulfur.[20]

The gas has a characteristic egg-like


odour.

Production
Hydrogen sulfide is most commonly
obtained by its separation from sour gas,
which is natural gas with a high content of
H2S. It can also be produced by treating
hydrogen with molten elemental sulfur at
about 450 °C. Hydrocarbons can serve as
a source of hydrogen in this process.[21]
Sulfate-reducing (resp. sulfur-reducing)
bacteria generate usable energy under
low-oxygen conditions by using sulfates
(resp. elemental sulfur) to oxidize organic
compounds or hydrogen; this produces
hydrogen sulfide as a waste product.

A standard lab preparation is to treat


ferrous sulfide with a strong acid in a Kipp
generator:

FeS + 2 HCl → FeCl2 + H2S

For use in qualitative inorganic analysis,


thioacetamide is used to generate H2S:

CH3C(S)NH2 + H2O → CH3C(O)NH2 + H2S


Many metal and nonmetal sulfides, e.g.
aluminium sulfide, phosphorus
pentasulfide, silicon disulfide liberate
hydrogen sulfide upon exposure to
water:[22]

6 H2O + Al2S3 → 3 H2S + 2 Al(OH)3

This gas is also produced by heating sulfur


with solid organic compounds and by
reducing sulfurated organic compounds
with hydrogen.

Water heaters can aid the conversion of


sulfate in water to hydrogen sulfide gas.
This is due to providing a warm
environment sustainable for sulfur
bacteria and maintaining the reaction
which interacts between sulfate in the
water and the water heater anode, which is
usually made from magnesium metal.[23]

Biosynthesis in the body

Hydrogen sulfide can be generated in cells


via enzymatic or non-enzymatic pathways.
H2S in the body acts as a gaseous
signaling molecule which is known to
inhibit Complex IV of the mitochondrial
electron transport chain which effectively
reduces ATP generation and biochemical
activity within cells.[24] Three enzymes are
known to synthesize H2S: cystathionine γ-
lyase (CSE), cystathionine β-synthetase
(CBS) and 3-mercaptopyruvate
sulfurtransferase (3-MST).[25] These
enzymes have been identified in a breadth
of biological cells and tissues, and their
activity has been observed to be induced
by a number of disease states.[26] It is
becoming increasingly clear that H2S is an
important mediator of a wide range of cell
functions in health and in diseases.[25]
CBS and CSE are the main proponents of
H2S biogenesis, which follows the trans-
sulfuration pathway.[27] These enzymes
are characterized by the transfer of a
sulfur atom from methionine to serine to
form a cysteine molecule.[27] 3-MST also
contributes to hydrogen sulfide production
by way of the cysteine catabolic
pathway.[26][27] Dietary amino acids, such
as methionine and cysteine serve as the
primary substrates for the transulfuration
pathways and in the production of
hydrogen sulfide. Hydrogen sulfide can
also be synthesized by non-enzymatic
pathway, which is derived from proteins
such as ferredoxins and Rieske
proteins.[26] There has been continuing
interest in exploiting such knowledge of
hydrogen sulfide's role in signaling through
development of mechanistically related
therapeutic agents.[28][29]
Hydrogen sulfide has been shown to be
involved in physiological processes such
as vasodilation in animals, as well as in
increasing seed germination and stress
responses in plants.[24] Hydrogen sulfide
signaling is also innately intertwined with
physiological processes that are known to
be moderated by reactive oxygen species
(ROS) and reactive nitrogen species
(RNS).[24] H2S has been shown to interact
with NO resulting in several different
cellular effects, as well as the formation of
a new signal called nitrosothiol.[24]
Hydrogen sulfide is also known to increase
the levels of glutathione which acts to
reduce or disrupt ROS levels in cells.[24]
The field of H2S biology has advanced
from environmental toxicology to
investigate the roles of endogenously
produced H2S in physiological conditions
and in various pathophysiological
states.[30] According to a current
classification, pathophysiological states
with H2S overproduction (such as cancer
and Down syndrome) and
pathophysiological states with H2S deficit
(e.g. vascular disease) can be
identified.[31] Although the understanding
of H2S biology has significantly advanced
over the last decade,[32][33][34] many
questions remain, for instance related to
the quantification of endogenous H2S
levels.[26]

Uses

Production of sulfur, thioorganic


compounds, and alkali metal sulfides

The main use of hydrogen sulfide is as a


precursor to elemental sulfur. Several
organosulfur compounds are produced
using hydrogen sulfide. These include
methanethiol, ethanethiol, and thioglycolic
acid.[21]

Upon combining with alkali metal bases,


hydrogen sulfide converts to alkali
hydrosulfides such as sodium hydrosulfide
and sodium sulfide:

H2S + NaOH → NaSH + H2O


NaSH + NaOH → Na2S + H2O

These compounds are used in the paper



making industry. Specifically, salts of SH
break bonds between lignin and cellulose
components of pulp in the Kraft
process.[21]

Reversibly sodium sulfide in the presence


of acids turns into hydrosulfides and
hydrogen sulfide; this supplies
hydrosulfides in organic solutions and is
utilized in the production of thiophenol.[35]
Analytical chemistry

For well over a century hydrogen sulfide


was important in analytical chemistry in
the qualitative inorganic analysis of metal
ions. In these analyses, heavy metal (and
nonmetal) ions (e.g., Pb(II), Cu(II), Hg(II),
As(III)) are precipitated from solution upon
exposure to H2S). The components of the
resulting precipitate redissolve with some
selectivity, and are thus identified.

Precursor to metal sulfides

As indicated above, many metal ions react


with hydrogen sulfide to give the
corresponding metal sulfides. This
conversion is widely exploited. For
example, gases or waters contaminated by
hydrogen sulfide can be cleaned with
metals, by forming metal sulfides. In the
purification of metal ores by flotation,
mineral powders are often treated with
hydrogen sulfide to enhance the
separation. Metal parts are sometimes
passivated with hydrogen sulfide.
Catalysts used in hydrodesulfurization are
routinely activated with hydrogen sulfide,
and the behavior of metallic catalysts used
in other parts of a refinery is also modified
using hydrogen sulfide.
Miscellaneous applications

Hydrogen sulfide is used to separate


deuterium oxide, or heavy water, from
normal water via the Girdler sulfide
process.

Scientists from the University of Exeter


discovered that cell exposure to small
amounts of hydrogen sulfide gas can
prevent mitochondrial damage. When the
cell is stressed with disease, enzymes are
drawn into the cell to produce small
amounts of hydrogen sulfide. This study
could have further implications on
preventing strokes, heart disease and
arthritis.[36]

Depending on the level of toning present,


coins that have been subject to toning by
hydrogen sulfide and other sulfur-
containing compounds may add to the
numismatic value of a coin based on the
toning's aesthetics. Coins can also be
intentionally treated with hydrogen sulfide
to induce toning, though artificial toning
can be distinguished from natural toning,
and is generally criticised among
collectors.[37]
A suspended animation-like state has
been induced in rodents with the use of
hydrogen sulfide, resulting in hypothermia
with a concomitant reduction in metabolic
rate. Oxygen demand was also reduced,
thereby protecting against hypoxia. In
addition, hydrogen sulfide has been shown
to reduce inflammation in various
situations.[38]

Occurrence

Deposit of sulfur on a rock, caused by


volcanic gas
Volcanoes and some hot springs (as well
as cold springs) emit some H2S, where it
probably arises via the hydrolysis of
sulfide minerals, i.e.
MS + H2O → MO + H2S. Hydrogen sulfide
can be present naturally in well water,
often as a result of the action of sulfate-
reducing bacteria.[39] Hydrogen sulfide is
produced by the human body in small
quantities through bacterial breakdown of
proteins containing sulfur in the intestinal
tract, therefore it contributes to the
characteristic odor of flatulence. It is also
produced in the mouth (halitosis).[40]
A portion of global H2S emissions are due
to human activity. By far the largest
industrial source of H2S is petroleum
refineries: The hydrodesulfurization
process liberates sulfur from petroleum by
the action of hydrogen. The resulting H2S
is converted to elemental sulfur by partial
combustion via the Claus process, which
is a major source of elemental sulfur.
Other anthropogenic sources of hydrogen
sulfide include coke ovens, paper mills
(using the Kraft process), tanneries and
sewerage. H2S arises from virtually
anywhere where elemental sulfur comes in
contact with organic material, especially at
high temperatures. Depending on
environmental conditions, it is responsible
for deterioration of material through the
action of some sulfur oxidizing
microorganisms. It is called biogenic
sulfide corrosion.

In 2011 it was reported that increased


concentrations of H2S were observed in
the Bakken formation crude, possibly due
to oil field practices, and presented
challenges such as "health and
environmental risks, corrosion of wellbore,
added expense with regard to materials
handling and pipeline equipment, and
additional refinement requirements".[41]
Besides living near gas and oil drilling
operations, ordinary citizens can be
exposed to hydrogen sulfide by being near
waste water treatment facilities, landfills
and farms with manure storage. Exposure
occurs through breathing contaminated air
or drinking contaminated water.[42]

In municipal waste landfill sites, the burial


of organic material rapidly leads to the
production of anaerobic digestion within
the waste mass and, with the humid
atmosphere and relatively high
temperature that accompanies
biodegradation, biogas is produced as
soon as the air within the waste mass has
been reduced. If there is a source of
sulfate bearing material, such as
plasterboard or natural gypsum (calcium
sulfate dihydrate), under anaerobic
conditions sulfate reducing bacteria
converts this to hydrogen sulfide. These
bacteria cannot survive in air but the
moist, warm, anaerobic conditions of
buried waste that contains a high source
of carbon – in inert landfills, paper and
glue used in the fabrication of products
such as plasterboard can provide a rich
source of carbon[43] – is an excellent
environment for the formation of hydrogen
sulfide.
In industrial anaerobic digestion
processes, such as waste water treatment
or the digestion of organic waste from
agriculture, hydrogen sulfide can be
formed from the reduction of sulfate and
the degradation of amino acids and
proteins within organic compounds.[44]
Sulfates are relatively non-inhibitory to
methane forming bacteria but can be
reduced to H2S by sulfate reducing
bacteria, of which there are several
genera.[45]
Removal from water

A number of processes have been


designed to remove hydrogen sulfide from
drinking water.[46]

Continuous chlorination
For levels up to 75 mg/L chlorine is used
in the purification process as an
oxidizing chemical to react with
hydrogen sulfide. This reaction yields
insoluble solid sulfur. Usually the
chlorine used is in the form of sodium
hypochlorite.[47]

Aeration
For concentrations of hydrogen sulfide
less than 2 mg/L aeration is an ideal
treatment process. Oxygen is added to
water and a reaction between oxygen
and hydrogen sulfide react to produce
odorless sulfate.[48]

Nitrate addition
Calcium nitrate can be used to prevent
hydrogen sulfide formation in
wastewater streams.

Removal from fuel gases

Hydrogen sulfide is commonly found in


raw natural gas and biogas. It is typically
removed by amine gas treating
technologies. In such processes, the
hydrogen sulfide is first converted to an
ammonium salt, whereas the natural gas
is unaffected.

+ −
RNH2 + H2S ⇌ [RNH3] + SH

The bisulfide anion is subsequently


regenerated by heating of the amine
sulfide solution. Hydrogen sulfide
generated in this process is typically
converted to elemental sulfur using the
Claus Process.
Process flow diagram of a typical amine treating process used in
petroleum refineries, natural gas processing plants and other
industrial facilities

Safety
Hydrogen sulfide is a highly toxic and
flammable gas (flammable range: 4.3–
46%). Being heavier than air, it tends to
accumulate at the bottom of poorly
ventilated spaces. Although very pungent
at first (it smells like rotten eggs[49]), it
quickly deadens the sense of smell,
creating temporary anosmia,[50] so victims
may be unaware of its presence until it is
too late. Safe handling procedures are
provided by its safety data sheet (SDS).[51]

Toxicity

Hydrogen sulfide is a broad-spectrum


poison, meaning that it can poison several
different systems in the body, although the
nervous system is most affected. The
toxicity of H2S is comparable with that of
carbon monoxide.[52] It binds with iron in
the mitochondrial cytochrome enzymes,
thus preventing cellular respiration. Its
toxic properties were described in detail in
1843 by Justus von Liebig.[53]

Low-level exposure

Since hydrogen sulfide occurs naturally in


the body, the environment, and the gut,
enzymes exist to metabolize it. At some
threshold level, believed to average around
300–350 ppm, the oxidative enzymes
become overwhelmed. Many personal
safety gas detectors, such as those used
by utility, sewage and petrochemical
workers, are set to alarm at as low as 5 to
10 ppm and to go into high alarm at 15
ppm. Metabolism causes oxidation to
sulfate, which is harmless.[54] Hence, low
levels of hydrogen sulfide may be tolerated
indefinitely.

Exposure to lower concentrations can


result in eye irritation, a sore throat and
cough, nausea, shortness of breath, and
fluid in the lungs (pulmonary edema).[52]
These effects are believed to be due to
hydrogen sulfide combining with alkali
present in moist surface tissues to form
sodium sulfide, a caustic.[55] These
symptoms usually subside in a few weeks.

Long-term, low-level exposure may result


in fatigue, loss of appetite, headaches,
irritability, poor memory, and dizziness.
Chronic exposure to low level H2S (around
2 ppm) has been implicated in increased
miscarriage and reproductive health
issues among Russian and Finnish wood
pulp workers,[56] but the reports have not
(as of 1995) been replicated.

High-level exposure

Short-term, high-level exposure can induce


immediate collapse, with loss of breathing
and a high probability of death. If death
does not occur, high exposure to hydrogen
sulfide can lead to cortical pseudolaminar
necrosis, degeneration of the basal
ganglia and cerebral edema.[52] Although
respiratory paralysis may be immediate, it
can also be delayed up to 72 hours.[57]
Diagnostic of extreme poisoning by H2S is
the discolouration of copper coins in the
pockets of the victim.

Inhalation of H2S resulted in about 7


workplace deaths per year in the U.S.
(2011–2017 data), second only to carbon
monoxide (17 deaths per year) for
workplace chemical inhalation deaths.[58]

Exposure thresholds

Exposure limits stipulated by the United


States government:[59]
10 ppm REL-Ceiling (NIOSH):
recommended permissible
exposure ceiling (the recommended
level that must not be exceeded,
except once for 10 min. in an 8-hour
shift, if no other measurable
exposure occurs)
20 ppm PEL-Ceiling (OSHA):
permissible exposure ceiling (the
level that must not be exceeded,
except once for 10 min. in an 8-hour
shift, if no other measurable
exposure occurs)
50 ppm PEL-Peak (OSHA): peak
permissible exposure (the level that
must never be exceeded)
100 ppm IDLH (NIOSH):
immediately dangerous to life and
health (the level that interferes with
the ability to escape)
0.00047 ppm or 0.47 ppb is the odor
threshold, the point at which 50% of a
human panel can detect the presence of
an odor without being able to identify
it.[60]
10–20 ppm is the borderline
concentration for eye irritation.
50–100 ppm leads to eye damage.
At 100–150 ppm the olfactory nerve is
paralyzed after a few inhalations, and
the sense of smell disappears, often
together with awareness of
danger.[61][62]
320–530 ppm leads to pulmonary
edema with the possibility of death.[52]
530–1000 ppm causes strong
stimulation of the central nervous
system and rapid breathing, leading to
loss of breathing.
800 ppm is the lethal concentration for
50% of humans for 5 minutes' exposure
(LC50).
Concentrations over 1000 ppm cause
immediate collapse with loss of
breathing, even after inhalation of a
single breath.

Treatment

Treatment involves immediate inhalation


of amyl nitrite, injections of sodium nitrite,
or administration of 4-
dimethylaminophenol in combination with
inhalation of pure oxygen, administration
of bronchodilators to overcome eventual
bronchospasm, and in some cases
hyperbaric oxygen therapy (HBOT).[52]
HBOT has clinical and anecdotal
support.[63][64][65]
Incidents

Hydrogen sulfide was used by the British


Army as a chemical weapon during World
War I. It was not considered to be an ideal
war gas, partially due to its flammability
and because the distinctive smell could be
detected from even a small leak, alerting
the enemy to the presence of the gas. It
was nevertheless used on two occasions
in 1916 when other gases were in short
supply.[66]

On September 2, 2005, a leak in the


propeller room of a Royal Caribbean Cruise
Liner docked in Los Angeles resulted in the
deaths of 3 crewmen due to a sewage line
leak. As a result, all such compartments
are now required to have a ventilation
system.[67][68]

A dump of toxic waste containing


hydrogen sulfide is believed to have
caused 17 deaths and thousands of
illnesses in Abidjan, on the West African
coast, in the 2006 Côte d'Ivoire toxic waste
dump.

In September 2008, three workers were


killed and two suffered serious injury,
including long term brain damage, at a
mushroom growing company in Langley,
British Columbia. A valve to a pipe that
carried chicken manure, straw and gypsum
to the compost fuel for the mushroom
growing operation became clogged, and
as workers unclogged the valve in a
confined space without proper ventilation
the hydrogen sulfide that had built up due
to anaerobic decomposition of the
material was released, poisoning the
workers in the surrounding area.[69]
Investigator said there could have been
more fatalities if the pipe had been fully
cleared and/or if the wind had changed
directions.[70]
In 2014, levels of hydrogen sulfide as high
as 83 ppm were detected at a recently
built mall in Thailand called Siam Square
One at the Siam Square area. Shop tenants
at the mall reported health complications
such as sinus inflammation, breathing
difficulties and eye irritation. After
investigation it was determined that the
large amount of gas originated from
imperfect treatment and disposal of waste
water in the building.[71]

In 2014, hydrogen sulfide gas killed


workers at the Promenade shopping
center in North Scottsdale, Arizona, USA
[72] after climbing into 15ft deep chamber
without wearing personal protective gear.
"Arriving crews recorded high levels of
hydrogen cyanide and hydrogen sulfide
coming out of the sewer."

In November 2014, a substantial amount


of hydrogen sulfide gas shrouded the
central, eastern and southeastern parts of
Moscow. Residents living in the area were
urged to stay indoors by the emergencies
ministry. Although the exact source of the
gas was not known, blame had been
placed on a Moscow oil refinery.[73]

In June 2016, a mother and her daughter


were found deceased in their still-running
2006 Porsche Cayenne SUV against a
guardrail on Florida's Turnpike, initially
thought to be victims of carbon monoxide
poisoning.[74][75] Their deaths remained
unexplained as the medical examiner
waited for results of toxicology tests on
the victims,[76] until urine tests revealed
that hydrogen sulfide was the cause of
death. A report from the Orange-Osceola
Medical Examiner's Office indicated that
toxic fumes came from the Porsche's
starter battery, located under the front
passenger seat.[77][78]

In January 2017, three utility workers in


Key Largo, Florida, died one by one within
seconds of descending into a narrow
space beneath a manhole cover to check a
section of paved street.[79] In an attempt to
save the men, a firefighter who entered the
hole without his air tank (because he could
not fit through the hole with it) collapsed
within seconds and had to be rescued by a
colleague.[80] The firefighter was airlifted
to Jackson Memorial Hospital and later
recovered.[81][82] A Monroe County Sheriff
officer initially determined that the space
contained hydrogen sulfide and methane
gas produced by decomposing
vegetation.[83]
On May 24, 2018, two workers were killed,
another seriously injured, and 14 others
hospitalized by hydrogen sulfide inhalation
at a Norske Skog paper mill in Albury, New
South Wales.[84][85] An investigation by
SafeWork NSW found that the gas was
released from a tank used to hold process
water. The workers were exposed at the
end of a 3-day maintenance period.
Hydrogen sulfide had built up in an
upstream tank, which had been left
stagnant and untreated with biocide
during the maintenance period. These
conditions allowed sulfate-reducing
bacteria to grow in the upstream tank, as
the water contained small quantities of
wood pulp and fiber. The high rate of
pumping from this tank into the tank
involved in the incident caused hydrogen
sulfide gas to escape from various
openings around its top when pumping
was resumed at the end of the
maintenance period. The area above it
was sufficiently enclosed for the gas to
pool there, despite not being identified as
a confined space by Norske Skog. One of
the workers who was killed was exposed
while investigating an apparent fluid leak
in the tank, while the other who was killed
and the worker who was badly injured
were attempting to rescue the first after he
collapsed on top of it. In a resulting
criminal case, Norske Skog was accused
of failing to ensure the health and safety of
its workforce at the plant to a reasonably
practicable extent. It pleaded guilty, and
was fined AU$1,012,500 and ordered to
fund the production of an anonymized
educational video about the
incident.[86][87][84][88]

In October 2019, an Odessa, Texas


employee of Aghorn Operating Inc. and his
wife were killed due to a water pump
failure. Produced water with a high
concentration of hydrogen sulfide was
released by the pump. The worker died
while responding to an automated phone
call he had received alerting him to a
mechanical failure in the pump, while his
wife died after driving to the facility to
check on him.[89] A CSB investigation cited
lax safety practices at the facility, such as
an informal lockout-tagout procedure and
a nonfunctioning hydrogen sulfide alert
system.[90]

Suicides

The gas, produced by mixing certain


household ingredients, was used in a
suicide wave in 2008 in Japan.[91] The
wave prompted staff at Tokyo's suicide
prevention center to set up a special
hotline during "Golden Week", as they
received an increase in calls from people
wanting to kill themselves during the
annual May holiday.[92]

As of 2010, this phenomenon has


occurred in a number of US cities,
prompting warnings to those arriving at
the site of the suicide.[93][94][95][96][97] These
first responders, such as emergency
services workers or family members are at
risk of death or injury from inhaling the
gas, or by fire.[98][99] Local governments
have also initiated campaigns to prevent
such suicides.
In 2020, H2S ingestion was used as a
suicide method by Japanese pro wrestler
Hana Kimura.[100]

Hydrogen sulfide in the


natural environment

Microbial: The sulfur cycle

Sludge from a pond; the black color is


due to metal sulfides

Hydrogen sulfide is a central participant in


the sulfur cycle, the biogeochemical cycle
of sulfur on Earth.[101]
In the absence of oxygen, sulfur-reducing
and sulfate-reducing bacteria derive
energy from oxidizing hydrogen or organic
molecules by reducing elemental sulfur or
sulfate to hydrogen sulfide. Other bacteria
liberate hydrogen sulfide from sulfur-
containing amino acids; this gives rise to
the odor of rotten eggs and contributes to
the odor of flatulence.

As organic matter decays under low-


oxygen (or hypoxic) conditions (such as in
swamps, eutrophic lakes or dead zones of
oceans), sulfate-reducing bacteria will use
the sulfates present in the water to oxidize
the organic matter, producing hydrogen
sulfide as waste. Some of the hydrogen
sulfide will react with metal ions in the
water to produce metal sulfides, which are
not water-soluble. These metal sulfides,
such as ferrous sulfide FeS, are often
black or brown, leading to the dark color of
sludge.

Several groups of bacteria can use


hydrogen sulfide as fuel, oxidizing it to
elemental sulfur or to sulfate by using
dissolved oxygen, metal oxides (e.g., iron
oxyhydroxides and manganese oxides), or
nitrate as electron acceptors.[102]
The purple sulfur bacteria and the green
sulfur bacteria use hydrogen sulfide as an
electron donor in photosynthesis, thereby
producing elemental sulfur. This mode of
photosynthesis is older than the mode of
cyanobacteria, algae, and plants, which
uses water as electron donor and liberates
oxygen.

The biochemistry of hydrogen sulfide is a


key part of the chemistry of the iron-sulfur
world. In this model of the origin of life on
Earth, geologically produced hydrogen
sulfide is postulated as an electron donor
driving the reduction of carbon dioxide.[103]
Animals

Hydrogen sulfide is lethal to most animals,


but a few highly specialized species
(extremophiles) do thrive in habitats that
are rich in this compound.[104]

In the deep sea, hydrothermal vents and


cold seeps with high levels of hydrogen
sulfide are home to a number of extremely
specialized lifeforms, ranging from
bacteria to fish.[105] Because of the
absence of sunlight at these depths, these
ecosystems rely on chemosynthesis rather
than photosynthesis.[106]
Freshwater springs rich in hydrogen
sulfide are mainly home to invertebrates,
but also include a small number of fish:
Cyprinodon bobmilleri (a pupfish from
Mexico), Limia sulphurophila (a poeciliid
from the Dominican Republic), Gambusia
eurystoma (a poeciliid from Mexico), and a
few Poecilia (poeciliids from
Mexico).[104][107] Invertebrates and
microorganisms in some cave systems,
such as Movile Cave, are adapted to high
levels of hydrogen sulfide.[108]
Interstellar and planetary occurrence

Hydrogen sulfide has often been detected


in the interstellar medium.[109] It also
occurs in the clouds of planets in our solar
system.[110][111]

Mass extinctions

A hydrogen sulfide bloom (green)


stretching for about 150km along the
coast of Namibia. As oxygen-poor
water reaches the coast, bacteria in
the organic-matter rich sediment
produce hydrogen sulfide, which is
toxic to fish.
Hydrogen sulfide has been implicated in
several mass extinctions that have
occurred in the Earth's past. In particular, a
buildup of hydrogen sulfide in the
atmosphere may have caused, or at least
contributed to, the Permian-Triassic
extinction event 252 million years
ago.[112][113][114]

Organic residues from these extinction


boundaries indicate that the oceans were
anoxic (oxygen-depleted) and had species
of shallow plankton that metabolized H2S.
The formation of H2S may have been
initiated by massive volcanic eruptions,
which emitted carbon dioxide and
methane into the atmosphere, which
warmed the oceans, lowering their
capacity to absorb oxygen that would
otherwise oxidize H2S. The increased
levels of hydrogen sulfide could have killed
oxygen-generating plants as well as
depleted the ozone layer, causing further
stress. Small H2S blooms have been
detected in modern times in the Dead Sea
and in the Atlantic ocean off the coast of
Namibia.[112]

See also
Hydrogen chalcogenide – any binary
compound of hydrogen with chalcogens,
including hydrogen polychalcogenides
Hydrogen sulfide chemosynthesis
Sewer gas – complex mixture of toxic
and nontoxic gases produced and
collected in sewage systems by the
decomposition of sewage
Targeted temperature management,
also known as induced hypothermia –
Medical procedure
Marsh gas

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Additional resources
Committee on Medical and Biological
Effects of Environmental Pollutants
(1979). Hydrogen Sulfide. Baltimore:
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External links
International Chemical Wikimedia
Commons
Safety Card 0165 (htt
has media
p://www.inchem.org/d related to
Hydrogen
ocuments/icsc/icsc/ei
sulfide.
cs0165.htm)
Concise International Chemical
Assessment Document 53 (http://www.i
nchem.org/documents/cicads/cicads/c
icad53.htm)
National Pollutant Inventory - Hydrogen
sulfide fact sheet (https://web.archive.or
g/web/20060309114102/http://www.np
i.gov.au/database/substance-info/profil
es/49.html)
NIOSH Pocket Guide to Chemical
Hazards (https://www.cdc.gov/niosh/np
g/npgd0337.html)
NACE (National Association of
Corrosion Epal) (https://www.nace.or
g/)
Retrieved from
"https://en.wikipedia.org/w/index.php?
title=Hydrogen_sulfide&oldid=1188705552"

This page was last edited on 7 December 2023, at


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