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Smoke AI simulator
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Smoke AI simulator
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Smoke
Smoke is an aerosol (a suspension of airborne particulates and gases) emitted when a material undergoes combustion or pyrolysis, together with the quantity of air that is entrained or otherwise mixed into the mass. It is commonly an unwanted by-product of fires (including stoves, candles, internal combustion engines, oil lamps, and fireplaces), but may also be used for pest control (fumigation), communication (smoke signals), defensive and offensive capabilities in the military (smoke screen), cooking, or smoking (tobacco, cannabis, etc.). It is used in rituals where incense, sage, or resin is burned to produce a smell for spiritual or magical purposes. It can also be a flavoring agent and preservative.
Smoke inhalation is the primary cause of death in victims of indoor fires. The smoke kills by a combination of thermal damage, poisoning and pulmonary irritation caused by carbon monoxide, hydrogen cyanide and other combustion products.
Smoke is an aerosol (or mist) of solid particles and liquid droplets that are close to the ideal range of sizes for Mie scattering of visible light.
The composition of smoke depends on the nature of the burning fuel and the conditions of combustion. Fires with high availability of oxygen burn at a high temperature and with a small amount of smoke produced; the particles are mostly composed of ash, or with large temperature differences, of condensed aerosol of water. High temperature also leads to production of nitrogen oxides. Sulfur content yields sulfur dioxide, or in case of incomplete combustion, hydrogen sulfide. Carbon and hydrogen are almost completely oxidized to carbon dioxide and water. Fires burning with lack of oxygen produce a significantly wider palette of compounds, many of them toxic. Partial oxidation of carbon produces carbon monoxide, while nitrogen-containing materials can yield hydrogen cyanide, ammonia, and nitrogen oxides. Hydrogen gas can be produced instead of water. Contents of halogens such as chlorine (e.g. in polyvinyl chloride or brominated flame retardants) may lead to the production of hydrogen chloride, phosgene, dioxin, and chloromethane, bromomethane and other halocarbons. Hydrogen fluoride can be formed from fluorocarbons, whether fluoropolymers subjected to fire or halocarbon fire suppression agents. Phosphorus and antimony oxides and their reaction products can be formed from some fire retardant additives, increasing smoke toxicity and corrosivity. Pyrolysis of polychlorinated biphenyls (PCB), e.g. from burning older transformer oil, and to lower degree also of other chlorine-containing materials, can produce 2,3,7,8-tetrachlorodibenzodioxin, a potent carcinogen, and other polychlorinated dibenzodioxins. Pyrolysis of fluoropolymers, e.g. teflon, in presence of oxygen yields carbonyl fluoride (which hydrolyzes readily to HF and CO2); other compounds may be formed as well, e.g. carbon tetrafluoride, hexafluoropropylene, and highly toxic perfluoroisobutene (PFIB).
Pyrolysis of burning material, especially incomplete combustion or smoldering without adequate oxygen supply, also results in production of a large amount of hydrocarbons, both aliphatic (methane, ethane, ethylene, acetylene) and aromatic (benzene and its derivates, polycyclic aromatic hydrocarbons; e.g. benzo[a]pyrene, studied as a carcinogen, or retene), terpenes. It also results in the emission of a range of smaller oxygenated volatile organic compounds (methanol, acetic acid, hydroxy acetone, methyl acetate and ethyl formate) which are formed as combustion by products as well as less volatile oxygenated organic species such as phenolics, furans and furanones. Heterocyclic compounds may be also present. Heavier hydrocarbons may condense as tar; smoke with significant tar content is yellow to brown. Combustion of solid fuels can result in the emission of many hundreds to thousands of lower volatility organic compounds in the aerosol phase. Presence of such smoke, soot, and/or brown oily deposits during a fire indicates a possible hazardous situation, as the atmosphere may be saturated with combustible pyrolysis products with concentration above the upper flammability limit, and sudden inrush of air can cause flashover or backdraft.
Presence of sulfur can lead to formation of gases like hydrogen sulfide, carbonyl sulfide, sulfur dioxide, carbon disulfide, and thiols; especially thiols tend to get adsorbed on surfaces and produce a lingering odor even long after the fire. Partial oxidation of the released hydrocarbons yields in a wide palette of other compounds: aldehydes (e.g. formaldehyde, acrolein, and furfural), ketones, alcohols (often aromatic, e.g. phenol, guaiacol, syringol, catechol, and cresols), carboxylic acids (formic acid, acetic acid, etc.).[citation needed]
The visible particulate matter in such smokes is most commonly composed of carbon (soot). Other particulates may be composed of drops of condensed tar, or solid particles of ash. The presence of metals in the fuel yields particles of metal oxides. Particles of inorganic salts may also be formed, e.g. ammonium sulfate, ammonium nitrate, or sodium chloride. Inorganic salts present on the surface of the soot particles may make them hydrophilic. Many organic compounds, typically the aromatic hydrocarbons, may be also adsorbed on the surface of the solid particles. Metal oxides can be present when metal-containing fuels are burned, e.g. solid rocket fuels containing aluminium. Depleted uranium projectiles after impacting the target ignite, producing particles of uranium oxides. Magnetic particles, spherules of magnetite-like ferrous ferric oxide, are present in coal smoke; their increase in deposits after 1860 marks the beginning of the Industrial Revolution. (Magnetic iron oxide nanoparticles can be also produced in the smoke from meteorites burning in the atmosphere.) Magnetic remanence, recorded in the iron oxide particles, indicates the strength of Earth's magnetic field when they were cooled beyond their Curie temperature; this can be used to distinguish magnetic particles of terrestrial and meteoric origin. Fly ash is composed mainly of silica and calcium oxide. Cenospheres are present in smoke from liquid hydrocarbon fuels. Minute metal particles produced by abrasion can be present in engine smokes. Amorphous silica particles are present in smokes from burning silicones; small proportion of silicon nitride particles can be formed in fires with insufficient oxygen. The silica particles have about 10 nm size, clumped to 70–100 nm aggregates and further agglomerated to chains. Radioactive particles may be present due to traces of uranium, thorium, or other radionuclides in the fuel; hot particles can be present in case of fires during nuclear accidents (e.g. Chernobyl disaster) or nuclear war.
Smoke particulates, like other aerosols, are categorized into three modes based on particle size:
Smoke
Smoke is an aerosol (a suspension of airborne particulates and gases) emitted when a material undergoes combustion or pyrolysis, together with the quantity of air that is entrained or otherwise mixed into the mass. It is commonly an unwanted by-product of fires (including stoves, candles, internal combustion engines, oil lamps, and fireplaces), but may also be used for pest control (fumigation), communication (smoke signals), defensive and offensive capabilities in the military (smoke screen), cooking, or smoking (tobacco, cannabis, etc.). It is used in rituals where incense, sage, or resin is burned to produce a smell for spiritual or magical purposes. It can also be a flavoring agent and preservative.
Smoke inhalation is the primary cause of death in victims of indoor fires. The smoke kills by a combination of thermal damage, poisoning and pulmonary irritation caused by carbon monoxide, hydrogen cyanide and other combustion products.
Smoke is an aerosol (or mist) of solid particles and liquid droplets that are close to the ideal range of sizes for Mie scattering of visible light.
The composition of smoke depends on the nature of the burning fuel and the conditions of combustion. Fires with high availability of oxygen burn at a high temperature and with a small amount of smoke produced; the particles are mostly composed of ash, or with large temperature differences, of condensed aerosol of water. High temperature also leads to production of nitrogen oxides. Sulfur content yields sulfur dioxide, or in case of incomplete combustion, hydrogen sulfide. Carbon and hydrogen are almost completely oxidized to carbon dioxide and water. Fires burning with lack of oxygen produce a significantly wider palette of compounds, many of them toxic. Partial oxidation of carbon produces carbon monoxide, while nitrogen-containing materials can yield hydrogen cyanide, ammonia, and nitrogen oxides. Hydrogen gas can be produced instead of water. Contents of halogens such as chlorine (e.g. in polyvinyl chloride or brominated flame retardants) may lead to the production of hydrogen chloride, phosgene, dioxin, and chloromethane, bromomethane and other halocarbons. Hydrogen fluoride can be formed from fluorocarbons, whether fluoropolymers subjected to fire or halocarbon fire suppression agents. Phosphorus and antimony oxides and their reaction products can be formed from some fire retardant additives, increasing smoke toxicity and corrosivity. Pyrolysis of polychlorinated biphenyls (PCB), e.g. from burning older transformer oil, and to lower degree also of other chlorine-containing materials, can produce 2,3,7,8-tetrachlorodibenzodioxin, a potent carcinogen, and other polychlorinated dibenzodioxins. Pyrolysis of fluoropolymers, e.g. teflon, in presence of oxygen yields carbonyl fluoride (which hydrolyzes readily to HF and CO2); other compounds may be formed as well, e.g. carbon tetrafluoride, hexafluoropropylene, and highly toxic perfluoroisobutene (PFIB).
Pyrolysis of burning material, especially incomplete combustion or smoldering without adequate oxygen supply, also results in production of a large amount of hydrocarbons, both aliphatic (methane, ethane, ethylene, acetylene) and aromatic (benzene and its derivates, polycyclic aromatic hydrocarbons; e.g. benzo[a]pyrene, studied as a carcinogen, or retene), terpenes. It also results in the emission of a range of smaller oxygenated volatile organic compounds (methanol, acetic acid, hydroxy acetone, methyl acetate and ethyl formate) which are formed as combustion by products as well as less volatile oxygenated organic species such as phenolics, furans and furanones. Heterocyclic compounds may be also present. Heavier hydrocarbons may condense as tar; smoke with significant tar content is yellow to brown. Combustion of solid fuels can result in the emission of many hundreds to thousands of lower volatility organic compounds in the aerosol phase. Presence of such smoke, soot, and/or brown oily deposits during a fire indicates a possible hazardous situation, as the atmosphere may be saturated with combustible pyrolysis products with concentration above the upper flammability limit, and sudden inrush of air can cause flashover or backdraft.
Presence of sulfur can lead to formation of gases like hydrogen sulfide, carbonyl sulfide, sulfur dioxide, carbon disulfide, and thiols; especially thiols tend to get adsorbed on surfaces and produce a lingering odor even long after the fire. Partial oxidation of the released hydrocarbons yields in a wide palette of other compounds: aldehydes (e.g. formaldehyde, acrolein, and furfural), ketones, alcohols (often aromatic, e.g. phenol, guaiacol, syringol, catechol, and cresols), carboxylic acids (formic acid, acetic acid, etc.).[citation needed]
The visible particulate matter in such smokes is most commonly composed of carbon (soot). Other particulates may be composed of drops of condensed tar, or solid particles of ash. The presence of metals in the fuel yields particles of metal oxides. Particles of inorganic salts may also be formed, e.g. ammonium sulfate, ammonium nitrate, or sodium chloride. Inorganic salts present on the surface of the soot particles may make them hydrophilic. Many organic compounds, typically the aromatic hydrocarbons, may be also adsorbed on the surface of the solid particles. Metal oxides can be present when metal-containing fuels are burned, e.g. solid rocket fuels containing aluminium. Depleted uranium projectiles after impacting the target ignite, producing particles of uranium oxides. Magnetic particles, spherules of magnetite-like ferrous ferric oxide, are present in coal smoke; their increase in deposits after 1860 marks the beginning of the Industrial Revolution. (Magnetic iron oxide nanoparticles can be also produced in the smoke from meteorites burning in the atmosphere.) Magnetic remanence, recorded in the iron oxide particles, indicates the strength of Earth's magnetic field when they were cooled beyond their Curie temperature; this can be used to distinguish magnetic particles of terrestrial and meteoric origin. Fly ash is composed mainly of silica and calcium oxide. Cenospheres are present in smoke from liquid hydrocarbon fuels. Minute metal particles produced by abrasion can be present in engine smokes. Amorphous silica particles are present in smokes from burning silicones; small proportion of silicon nitride particles can be formed in fires with insufficient oxygen. The silica particles have about 10 nm size, clumped to 70–100 nm aggregates and further agglomerated to chains. Radioactive particles may be present due to traces of uranium, thorium, or other radionuclides in the fuel; hot particles can be present in case of fires during nuclear accidents (e.g. Chernobyl disaster) or nuclear war.
Smoke particulates, like other aerosols, are categorized into three modes based on particle size:
