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Benzene

DESIGNATIONS

CAS No.: 71-43-2
Registry name: Benzene
Chemical name: Benzene
Synonyms,Tradenames: Benzol, bicarburate of hydrogen, carbon oil, coal naphtha, cyclohexatriene, mineral naphtha, motor benzol, phene, phenyl hydride
Chemical name (German): Benzol, Benzen
Chemical name (French): Benzčne
Appearance: colourless, highly volatile liquid with aromatic odour

BASIC CHEMICAL AND PHYSICAL DATA

Empirical formula: C6H6
Rel. molecular mass: 78.12 g
Density: 0.879 g/cm3
Relative gas density: 2.7
Boiling point: 80.1°C
Melting point: 5.5°C
Vapour pressure: 102 hPa
Flash point: -11°C
Ignition temperature: 555°C
Solvolysis/solubility: in water: 1.79 g/l (25°C)

soluble in fats

miscible with acetone, ether, alcohol, chloroform

Conversions factors: 1 ppm = 3.26 mg/m3 at 20°C

1 mg/m3 = 0.31 ppm

ORIGIN AND USE

Usage:
In the chemical industry pure benzene forms the most important basis for aromatic intermediate products as well as for the group of cycloaliphatic compounds. Plastics, synthetic rubber, dyes, paints, varnishes, resins, detergent raw materials and pesticides are all produced on the basis of benzene.

Origin/derivation:
Benzene is found in small quantities and at low concentrations in nature. It is a component part of crude oil (max. 0.4 g/l). Benzene is produced and processed on a large scale as pure benzene. It is normally obtained from crude oil. Standard grade petrol contains between 12 and 16 g/l, premium petrol up to 24 g/l of benzene. Emission sources apart from motor vehicles are coking plants, furnaces, refineries and the chemical industry in addition to the storage and distribution of petrol.

Production figures:
The estimated figures for overall worldwide annual production vary. They are estimated at more than 15 million tons of pure benzene and some 10 million tons in fuels. Production of pure benzene:

D (1983): 1.34 mio t EC (1978/79): 4.4 mio t
F (1983) 1.37 mio t USA (1983) 4.28 mio t
Japan (1983) 1.75 mio t USSR (1977) 1.54 mio t

Emission figures (estimated):
Worldwide 100,000-1,000,000 t/a; USA into atmosphere 110,000-224,000 t/a (of which 40,000-80,000 t/a from fuels); USA into surface/groundwater 3-14 t/a; D 55,000-70,000 t/a (of which 50,000-60,000 t/a from fuels)

Toxicity

Humans: TLC0 0.68 mg/l, inhalation 1)
Mammals:
Rat (male) LD50 3.8-6.5 g/kg, oral
Rat (male) LD50 17.6 g/kg, dermal
Rat (male) LC50 18 mg/l, inhalation (4 h)
Rat (female) LD50 6.2-7.2 g/kg, oral
Rat (female) LD50 19.4 g/kg, dermal
Rat (female) LC50 23 mg/l, inhalation (4 h)
Insects:
Weevil LC50 210 mg/l
Aquatic organisms:
Golden orfe LC0 31 +/- 25 mg/l (96 h) (ringtest, 11 laboratories)
Goldfish LC0 36 mg/l (24 h)
Trout LC50 22 mg/l (96 h)
Herring EC0 <0.8 mg/l (reproduction)
Water flea (Daphnia magna) LC50 200 mg/l (48 h)
Water flea (Daphnia magna) LC50 15 mg/l (96 h)
Blue algae EC0 >1400 mg/l (inhibition of cell reproduction)
Green algae EC0 >1400 mg/l (inhibition of cell reproduction)
Green algae EC50 310-460 mg/l (reduced photosynthesis)
Marine algae EC0 approx. 1400 mg/l (reduced productivity)
Other organisms:
Earthworm LC50 100-1000 µg/cm2 (48 h)

Note: 1) All data as per RIPPEN, 1989

Characteristic effects:
Humans/mammals: The inhalation of benzene vapours may affect the central nervous system depending on the concentration and the duration of exposure. The symptoms of acute poisoning are dizziness, headaches, nausea, drowsiness and disturbance of consciousness with states of agitation and spasms, finally resulting in loss of consciousness and paralysis of the respiratory centre. Liquid benzene irritates the skin and mucous membranes and may be resorbed through the skin.

Chronic exposure causes damage to bone marrow. Benzene is a blood toxin: chromosomal changes in blood corpuscles of workers subjected to exposure and in blood corpuscles and bone cells of rats subjected to exposure have been found.

Proven carcinogenity in humans; carcinogenic tumours in rats and mice;

Plants: High atmospheric concentrations (>50 mg/m3, 30 min.) have a lethal effect. In water used for watering plants, small benzene concentrations stimulate plant growth and root formation. On the other hand, high concentrations close to the saturated solution inhibit growth.

Note: A detailed list of the investigations performed to establish the characteristic effects of benzene can be found in OAK RIDGE NATIONAL LABORATORY, 1987 and BUA, 1988.

ENVIRONMENTAL BEHAVIOUR

Water:
Benzene is highly volatile: evaporation half-life 2.7-5 hours (4.8 h in 1m deep body of water at 25°C).

Air:
Benzene is a moderate source of smog. It readily reacts with OH radicals, whose concentration governs the dwell time in the atmosphere (between several hours and several days). Wash-out effects merely result in short-term extraction from the atmosphere since benzene readily evaporates again from the surface of water or soil.

Soil:
Benzene is highly volatile and thus considerable losses from the topsoil into the atmosphere take place. In deeper soil layers, the substance is relatively mobile. Thus, elution into groundwater may result. Benzene accumulates in sewage sludge.

Degradation, decomposition products, half-life:
Degradation in the atmosphere primarily takes place by indirect phototransformation; no photolysis at wavelengths >290nm. In the troposphere the half-life is between 7 and 22 days with a mean value of 13 days. In the lower troposphere (up to an altitude of approx. 1-2 km), the average values for the half-life of benzene are between 3 and 10 days.

Degradation in surface water, groundwater and in soil is mainly by way of biodegradation (aerobic more readily than anaerobic). Microbial metabolites: 1,2-dihydroxy-1,2-dihydrobenzene, pyrocatechol. Metabolites in mammals: Phenols and related compounds (e.g. hydroquinone, pyrocatechol). 33% aerobic degradation in sewage treatment plants after 12h; aerobic degradation is slight compared to volatilisation. Thermal decomposition takes place at 600°C in the vapour phase; hydrolysis is unlikely under normal conditions.

ENVIRONMENTAL STANDARDS

Medium/acceptor Sector Country/organ.

Status

Value Cat. Remarks Source
Water:   D

G

3 WGK   acc. RIPPEN, 1989
Drinkw A

L

10 µg/l     acc. RIPPEN, 1989
Drinkw SU

G

500 µg/l   Tox. tolerance value acc. RIPPEN, 1989
Drinkw USA

G

13 µg/l (7d)   Nat. Acad. Science acc. RIPPEN, 1989
Drinkw USA

G

0.35 µg/l (7d)   U.S.EPA acc. RIPPEN, 1989
Drinkw USA

G

0.67 µg/l   Chron. exposure acc. RIPPEN, 1989
Drinkw USA

(L)

5 µg/l MCL    
Drinkw WHO

G

10 µg/l   Risk of leukaemia WHO, 1984
Waste water USA

G

125 µg/l   Direct introduction acc. RIPPEN, 1989
Waste water USA

G

75 µg/l (average, 4d) Direct introduction acc. RIPPEN, 1989
Groundw D(HH)

G

1 µg/l   Closer investigation acc. LAU-BW1), 1989
Groundw D(HH)

G

5 µg/l   Rehabilitation investigation acc. LAU-BW1), 1989
Groundw NL

G

0.2 µg/l   Reference acc. TERRA TECH 6/94
Groundw NL

L

30 µg/l   Intervention acc. TERRA TECH 6/94
Groundw USA

L

1 µg/l   Florida acc. ORNL2), 1987
Surface USA

G

3.1 mg/l (1 d, average) Protect. of freshwater acc. RIPPEN, 1989
Surface USA

G

7 mg/l (max.) Protect. of freshwater acc. RIPPEN, 1989
Surface USA

G

0.92 mg/l (1 d, average) Protect. of saltwater acc. RIPPEN, 1989
Surface USA

G

2.1 mg/l (max.) Protect. of saltwater acc. RIPPEN, 1989
Soil:   NL

G

0.05 mg/kg DM   Reference acc. TERRA TECH 6/94
  NL

L

1 mg/kg DM   Intervention acc. TERRA TECH 6/94
Air: Emiss. D

L

5 mg/m3   mass flow > 25 g/h acc. TA Luft, 1986
  D

L

10 mg/m3 MIK Short-time value acc. RIPPEN, 1989
  D

L

3 mg/m3 MIK Long-time value acc. RIPPEN, 1989
  DDR

(L)

0.3 mg/m3 (MIK) Short-time value acc. HORN et al., 1989
  DDR

(L)

0.1 mg/m3 (MIK) Long-time value acc. HORN et al., 1989
  H

(L)

0.8 mg/m3   30 min average3) acc. STERN, 1986
  H

(L)

1 mg/m3   30 min average4) acc. STERN, 1986
  H

(L)

0.3 mg/m3   24 h average4) acc. STERN, 1986
  IL

(L)

4.8 mg/m3   30 min average acc. STERN, 1986
  IL

(L)

1.6 mg/m3   24 h average acc. STERN, 1986
  PL

(L)

0.2 mg/m3   30 min average3) acc. STERN, 1986
  PL

(L)

1 mg/m3   30 min average4) acc. STERN, 1986
  PL

(L)

0.1 mg/m3   24 h average3) acc. STERN, 1986
  PL

(L)

0.3 mg/m3   24 h average4) acc. STERN, 1986
  PL

(L)

0.025 mg/m3   a-average3) acc. STERN, 1986
  PL

(L)

0.043 mg/m3   a-average4) acc. STERN, 1986
  RO

(L)

2.4 mg/m3   30 min average acc. STERN, 1986
  RO

(L)

0.8 mg/m3   24 h average acc. STERN, 1986
  SU

(L)

1 mg/m3   30 min average4) acc. STERN, 1986
  SU

(L)

0.3 mg/m3   24 h average4) acc. STERN, 1986
Workp CS

(L)

16 ppm   from 1969 acc. ACGIH, 1982
Workp D

L

16 mg/m3 TRK5)   DFG, 1989
Workp D

L

5 ml/m3 TRK6)   DFG, 1989
Workp DDR

(L)

5 mg/m3     acc. HORN et al, 1988
Workp S

(L)

10 ppm   from 1975 acc. ACGIH, 1982
Workp SU

(L)

5 mg/m3     acc. RIPPEN, 1989
Workp USA

(L)

10 ppm TWA   acc. AUER TECHNIKUM 1988

Note:

1) Baden-Württemberg Regional Environment Office
2) Oak Ridge National Laboratory
3) Specially protected areas
4) Protected areas
5) Dusts
6) Gases and vapours

Further benzene-specific legislation in the Federal Republic of Germany can be found in:
the Gefahrstoffverordnung (Ordinance on Hazardous Substances), the Bundesimmissionsschutzverordnung (Federal Immission Control Ordinance); the Störfallverordnung (Hazardous Incident Ordinance), the Gefahrgutverordnungen (ordinances governing hazardous materials), the Abfallgesetz-Sonderabfall (Waste Avoidance and Waste Management Act - Special Waste), the Benzinqualitätsangabeverordnung (ordinance on the indication of fuel grade), the Kosmetikverordnung (ordinance on cosmetics), the Verordnung über die Einschränkung und Verbote für bestimmte Stoffe in Spielwaren und Scherzartikeln (ordinance on the restriction and banning of certain substances in toys and joke-shop articles).

Comparison/reference values

Medium/origin Country Value
Water
Rhine (Basle, 1976) CH 0.2 µg/l
Rhine (Cologne, 1976) D 0.3 µg/l
Rhine (Duisburg, 1976) D 0.8 µg/l
Tees River Estuary (1984) GB 0.1-200 µg/l
Groundwater (not contaminated) NL <0.01-0.03 µg/l (n=8)
Groundwater (contaminated) NL 100 µg/l
Groundwater (contaminated) USA 1.0-470 µg/l (n=9 of 13)
Dump seepage water USA 17-540 µg/l (n=6)
Drinking water USA <0.5-15 µg/l (n=945; 11 >=0.5 µg/l)
Rainwater GB 87 µg/l
Soil/sediment:
Sewage sludge USA 0.05-11.3 mg/kg (n=11 of 13)
Tees River Estuary (1986) GB 1.5-3.9 µg/kg (n=4)
Air:
Clean air, Southern hemisphere 1980-1983 <5-80 pptv (average values)
Clean air, Northern hemisphere 1980-1983 100-260 pptv (average values)
Arctic (July 1982)   66 pptv (n=8; average value)
Arctic (spring 1983)   307 pptv (n=10; average value)
Deuselbach ('clean air', 1983) D 0.10-0.12 ppbv (average values)
Various (background impact) Brazil 0.31-0.72 ppbv (n=8)
Various Kenya 0.07-0.85 ppbv (n=13)
Various (desert) Egypt 0.19 ppbv (n=5; average value)
Berlin (1976/77) D 0.6-60 ppbv (n>200; 24 h values)
7 cities (1980/81) USA 1.4-5.8 ppbv (average values)
Leningrad (1977-79) SU 5.4-204 ppbv (n=30; 20-50 min values)
Respiratory air:
At petrol stations (1970-80)   100-10,000 µg/ m3 (n>130; 2-14 h values)
Petrol-tanker drivers   30-100,000 µg/m3
Petrol-tanker drivers   540 µg/m3 (8 h average value)
Tanker crew   2,400-170,000 µg/m3
Tanker crew   4200 µg/m3 (8 h average value)
Foodstuffs:
Various fish (Los Angeles Bay, 1980/81) <1-52 µg/kg FS (n=4)
Eggs   0.5-1.9 mg/kg
Beef   2-19 µg/kg
Rum   0.12 µg/kg

Note: 1) All data as per RIPPEN, 1989

Assessment/comments

In view of the fact that benzene readily ingresses into the atmosphere on account of its physical properties, it can be transported over long distances despite relatively short transformation reactions. The advantages of relatively rapid benzene degradation are offset by numerous toxic degradation products. In addition to workplace exposure, humans are threatened above all by the intake of benzene caused by smoking and traffic emissions. The limit values and guide values vary in the atmospheric sector and particularly in the drinking water sector. The values recommended by the WHO are 15 - 30 times in excess of the proposals made by the U.S. EPA which should be used for orientation at least in those instances where drinking water is primarily used for human consumption.

Further information on benzene is to be found in RIPPEN (1989), OAK RIDGE NATIONAL LABORATORY (1987) and BUA, 1988.


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