How quickly does benzene decompose?
According to one experiment, benzene has a half-life of 17 days due to photodegradation which could contribute to benzene’s removal in situations of cold water, poor nutrients, or other conditions less conductive to microbial degradation.
Does benzene evaporate fast?
Benzene evaporates into the air very quickly. Its vapor is heavier than air and may sink into low-lying areas. Benzene dissolves only slightly in water and will float on top of water.
How much benzene is in a cigarette ppm?
Benzene emissions from cigarette smoking range from 430 to 590 μg per cigarette (28). An increase in benzene concentration of at least 30–70% is expected (3,18,20,29,30) when ETS is present indoors, with increases in some cases of 300% (31) to levels of 16 μg/m3 (18).
What is the half life of benzene?
Degradation in the atmosphere occurs primarily by indirect phototransformation. With high stability and minimal reactivity, the half-life of benzene in the atmosphere can range from 3 to 10 days (tropospheric half-life is 7–22 days), enabling it to be transported locally and regionally.
What is the short-term exposure limit for benzene?
NIOSH: The recommended airborne exposure limit (REL) is 0.1 ppm averaged over a 10-hour workshift and 1 ppm, not to be exceeded during any 15-minute work period. ACGIH: The threshold limit value (TLV) is 0.5 ppm averaged over an 8-hour workshift and 2.5 ppm as a STEL (short-term exposure limit).
At what temperature does benzene evaporate?
It has a relatively low boiling point (80.1 oC) and a high vapour pressure (9.95 kPa at 20 oC), causing it to evaporate rapidly at room temperature. It is slightly soluble in water (1.8 g/litre at 25 oC) and miscible with most organic solvents.
Why benzene is volatile?
Benzene belongs to a class of chemicals called volatile organic compounds, so called because they evaporate in the air. Benzene is made from coal and petroleum sources and is present in gasoline.
What makes benzene carcinogenic?
Benzene has been shown to cause chromosome changes in bone marrow cells in the lab. (The bone marrow is where new blood cells are made.) Such changes are commonly found in human leukemia cells.
At what ppm can you smell benzene?
1.5 to 4.7 ppm
Benzene has a sweet, aromatic, gasoline-like odor. Most individuals can begin to smell benzene in air at 1.5 to 4.7 ppm. The odor threshold generally provides adequate warning for acutely hazardous exposure concentrations but is inadequate for more chronic exposures.
How many ppm is benzene harmful?
Basis for revised IDLH: The revised IDLH for benzene is 500 ppm based on acute inhalation toxicity data in humans [Gerarde 1960].
What is the range of petrol in benzene?
US Environmental Protection Agency (EPA) limits the Benzene percentage in gasoline to an average of 0.62% by volume (maximum 1.3%). The Fuels Quality Directive (EU, 2003a) limits the Benzene content in petrol to < 1%.
At what temperature does benzene become a gas?
Chemical, physical and thermal properties of benzene, also called benzol. Phase diagram included.
Property | Value | Value |
---|---|---|
Heat (enthalpy) of sublimation, at 42°F/5.85°C | 45 | 576 |
Heat (enthalpy) of evaporation | 33.8 | 433 |
Specific heat capacity, Cp (gas) | 82.4 | 1.05 |
Specific heat capacity, Cp (liquid) | 133 | 1.70 |
Why does methylbenzene react faster?
Methylbenzene is more reactive than benzene because of the tendency of the methyl group to “push” electrons towards the ring. The effect of this greater reactivity is that methylbenzene will react with fuming sulfuric acid at 0°C, and with concentrated sulfuric acid if they are heated under reflux for about 5 minutes.
What happens when benzene is burned in oxygen?
Liquid benzene burns in oxygen according to 2C6H6(l)+15O2(g)→12CO2(g)+6H2O(l).
Which is more volatile benzene or toluene?
At atmospheric pressure, the bubble temperature for benzene [Teb(1) = 353 K] is lower than that of toluene [Teb(2) = 384 K]. Therefore, it can be said that benzene is more volatile than toluene.
Which process is most easily done on benzene?
Hence, benzene undergo electrophilic substitution reactions easily and nucleophilic substitutions with difficulty.