Pes Smoke Patch
Skyy Mansour
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This map is a collaborative effort between the U.S. Environmental Protection Agency (EPA), led by Ron Evans, and the U.S. Forest Service (USFS) led Interagency Wildland Fire Air Quality Response Program, led by Pete Lahm, USFS. Development work led by Sim Larkin, USFS, and Stuart Illson, University of Washington, in collaboration with the EPA AirNow Team. Correction equation work was led by Karoline Barkjohn, EPA. Additional thanks to Jonathan Callahan, Desert Research Institute, Marlin Martnez, University of Washington, and many others. This site relies on data provided from a number of sources, including AirNow, the Western Regional Climate Center, AirSis, and PurpleAir for monitoring and sensor data, and the NOAA Hazard Mapping System and National Interagency Fire Center for fire and smoke plume information. Feedback and questions can be directed to firesm...@epa.gov.
Monitor permanent: and temporary: icons and sensors icons on the Fire and Smoke Map show particle pollution in the color codes of the U.S. Air Quality Index (AQI). Click on an icon to see the NowCast AQI level at that location, and to see actions to consider taking.
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Smoke is a suspension[3] of airborne particulates and gases[4] 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.
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.[6] Sulfur content yields sulfur dioxide, or in case of incomplete combustion, hydrogen sulfide.[7] Carbon and hydrogen are almost completely oxidized to carbon dioxide and water.[8] Fires burning with lack of oxygen produce a significantly wider palette of compounds, many of them toxic.[8] Partial oxidation of carbon produces carbon monoxide, while nitrogen-containing materials can yield hydrogen cyanide, ammonia, and nitrogen oxides.[9] Hydrogen gas can be produced instead of water.[9] 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.[9][10] 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.[10] 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.[10] 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).[11]
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.[12] 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.[1] Heterocyclic compounds may be also present.[13] Heavier hydrocarbons may condense as tar; smoke with significant tar content is yellow to brown.[14] Combustion of solid fuels can result in the emission of many hundreds to thousands of lower volatility organic compounds in the aerosol phase.[15] 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.[16]
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]
Most of the smoke material is primarily in coarse particles. Those undergo rapid dry precipitation, and the smoke damage in more distant areas outside of the room where the fire occurs is therefore primarily mediated by the smaller particles.[20]
Burning of hydrogen-rich fuel produces water vapor; this results in smoke containing droplets of water. In absence of other color sources (nitrogen oxides, particulates...), such smoke is white and cloud-like.
Smoke emissions may contain characteristic trace elements. Vanadium is present in emissions from oil fired power plants and refineries; oil plants also emit some nickel. Coal combustion produces emissions containing aluminium, arsenic, chromium, cobalt, copper, iron, mercury, selenium, and uranium.
Traces of vanadium in high-temperature combustion products form droplets of molten vanadates. These attack the passivation layers on metals and cause high temperature corrosion, which is a concern especially for internal combustion engines. Molten sulfate and lead particulates also have such effect.
Some components of smoke are characteristic of the combustion source. Guaiacol and its derivatives are products of pyrolysis of lignin and are characteristic of wood smoke; other markers are syringol and derivates, and other methoxy phenols. Retene, a product of pyrolysis of conifer trees, is an indicator of forest fires. Levoglucosan is a pyrolysis product of cellulose. Hardwood vs softwood smokes differ in the ratio of guaiacols/syringols. Markers for vehicle exhaust include polycyclic aromatic hydrocarbons, hopanes, steranes, and specific nitroarenes (e.g. 1-nitropyrene). The ratio of hopanes and steranes to elemental carbon can be used to distinguish between emissions of gasoline and diesel engines.[21]
Many compounds can be associated with particulates; whether by being adsorbed on their surfaces, or by being dissolved in liquid droplets. Hydrogen chloride is well absorbed in the soot particles.[20]
Deposited hot particles of radioactive fallout and bioaccumulated radioisotopes can be reintroduced into the atmosphere by wildfires and forest fires; this is a concern in e.g. the Zone of alienation containing contaminants from the Chernobyl disaster.
Polymers are a significant source of smoke. Aromatic side groups, e.g. in polystyrene, enhance generation of smoke. Aromatic groups integrated in the polymer backbone produce less smoke, likely due to significant charring. Aliphatic polymers tend to generate the least smoke, and are non-self-extinguishing. However presence of additives can significantly increase smoke formation. Phosphorus-based and halogen-based flame retardants decrease production of smoke. Higher degree of cross-linking between the polymer chains has such effect too.[22]
The naked eye detects particle sizes greater than 7 μm (micrometres).[23] Visible particles emitted from a fire are referred to as smoke. Invisible particles are generally referred to as gas or fumes. This is best illustrated when toasting bread in a toaster. As the bread heats up, the products of combustion increase in size. The fumes initially produced are invisible but become visible if the toast is burnt.
An ionization chamber type smoke detector is technically a product of combustion detector, not a smoke detector. Ionization chamber type smoke detectors detect particles of combustion that are invisible to the naked eye. This explains why they may frequently false alarm from the fumes emitted from the red-hot heating elements of a toaster, before the presence of visible smoke, yet they may fail to activate in the early, low-heat smoldering stage of a fire.
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