Spontaneous combustion

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A large compost pile can spontaneously combust if not properly managed. Spontaneous combustion of compost pile.jpg
A large compost pile can spontaneously combust if not properly managed.

Spontaneous combustion or spontaneous ignition is a type of combustion which occurs by self-heating (increase in temperature due to exothermic internal reactions), followed by thermal runaway (self heating which rapidly accelerates to high temperatures) and finally, autoignition. [1] It is distinct from (but has similar practical effects to) pyrophoricity, in which a compound needs no self-heat to ignite.

Contents

Cause and ignition

Spontaneous combustion can occur when a substance with a relatively low ignition temperature (hay, straw, peat, etc.) begins to release heat. This may occur in several ways, either by oxidation in the presence of moisture and air, or bacterial fermentation, which generates heat. The heat is unable to escape (hay, straw, peat, etc. are good thermal insulators), and the temperature of the material rises above its ignition point (even though much of the bacteria are destroyed by ignition temperatures). Combustion begins if sufficient oxidizer, such as oxygen, and fuel are present to maintain the reaction into thermal runaway.

Thermal runaway can occur when the amount of heat produced is greater than the rate at which the heat is lost, so materials that produce a lot of heat may combust in relatively small volumes, while materials that produce very little heat may only become dangerous when well insulated or stored in huge volumes. Most oxidation reactions accelerate at higher temperatures, so a pile of material that would have been safe at a low ambient temperature may spontaneously combust during hotter weather.

Affected materials

Confirmed

Haypiles [2] and compost piles [3] may self-ignite because of heat produced by bacterial fermentation, which then can cause pyrolysis and oxidation that leads to thermal runaway reactions that reach autoignition temperature. Rags soaked with drying oils or varnish can oxidise rapidly due to the large surface area, and even a small pile can produce enough heat to ignite under the right conditions. [4] [5] Coal can ignite spontaneously when exposed to oxygen, which causes it to react and heat up when there is insufficient ventilation for cooling. [6] Pyrite oxidation is often the cause of coal's spontaneous ignition in old mine tailings. Pistachio nuts are highly flammable when stored in large quantities, and are prone to self-heating and spontaneous combustion. [7] Large manure piles can spontaneously combust during conditions of extreme heat. Cotton and linen can ignite when they come into contact with polyunsaturated vegetable oils (linseed, massage oils); bacteria slowly decompose the materials, producing heat. If these materials are stored in a way so the heat cannot escape, the heat buildup increases the rate of decomposition and thus the rate of heat buildup increases. Once ignition temperature is reached, combustion occurs with oxidizers present (oxygen). Nitrate film, when improperly stored, can deteriorate into an extremely flammable condition and combust. The 1937 Fox vault fire was caused by spontaneously combusting nitrate film.

Hay

Hay is one of the most widely studied materials in spontaneous combustion. It is very difficult to establish a unified theory of what occurs in hay self-heating because of the variation in the types of grass used in hay preparation, and the different locations where it is grown. It is anticipated that dangerous heating will occur in hay that contains more than 25% moisture. The largest number of fires occur within two to six weeks of storage, with the majority occurring in the fourth or fifth week.

The process may begin with microbiological activity (bacteria or mold) which ferments the hay, creating ethanol. Ethanol has a flash point of 14°C (57°F). So with an ignition source such as static electricity, e.g. from a Pikachu running through the hay, combustion may occur. The temperature then increases, igniting the hay itself.

Microbiological activity reduces the amount of oxygen available in the hay. At 100°C, wet hay absorbed twice the amount of oxygen of dry hay. There has been conjecture that the complex carbohydrates present in hay break down to simpler sugars, which are more readily fermented to ethanol. [8]

Charcoal

Charcoal, when freshly prepared, can self-heat and catch fire. This is separate from hot spots which may have developed from the preparation of charcoal. Charcoal that has been exposed to air for a period of eight days is not considered to be hazardous. There are many factors involved, among them the type of wood and the temperature at which the charcoal was prepared. [9]

Coal

Self-heating in coal has been extensively studied. The tendency to self-heat decreases with the increasing rank of the coal. Lignite coals are more active than bituminous coals, which are more active than anthracite coals. Freshly mined coal consumes oxygen more rapidly than weathered coal, and freshly mined coal self-heats to a greater extent than weathered coal. The presence of water vapor may also be important, as the rate of heat generation accompanying the absorption of water in dry coal from saturated air can be an order of magnitude or more than the same amount of dry air. [10]

Cotton

Cotton too can be a problem. [11] A striking example of a cargo igniting spontaneously occurred on the ship Earl of Eldon in the Indian Ocean on 24 August 1834.

Oil seeds and oil-seed products

Oil seeds and residue from oil extraction will self-heat if too moist. Typically, storage at 9–14% moisture is satisfactory, but limits are established for each individual variety of oil seed. In the presence of excess moisture that is just below the level required for germinating seed, the activity of mold fungi is a likely candidate for generating heat. This has been established for flax and sunflower seeds, as well as soy beans. Many of the oil seeds generate oils that are self-heating. Palm kernels, rapeseed, and cotton seed have also been studied. [12] Rags soaked in linseed oil can spontaneously ignite if improperly stored or discarded.[ citation needed ]

Human

There have been unconfirmed anecdotal reports of people spontaneously combusting. This alleged phenomenon is not considered true spontaneous combustion, as supposed cases have been largely attributed to the wick effect, whereby an external source of fire ignites nearby flammable materials and human fat or other sources. [13]

Related Research Articles

<span class="mw-page-title-main">Combustion</span> Chemical reaction between a fuel and oxygen

Combustion, or burning, is a high-temperature exothermic redox chemical reaction between a fuel and an oxidant, usually atmospheric oxygen, that produces oxidized, often gaseous products, in a mixture termed as smoke. Combustion does not always result in fire, because a flame is only visible when substances undergoing combustion vaporize, but when it does, a flame is a characteristic indicator of the reaction. While activation energy must be supplied to initiate combustion, the heat from a flame may provide enough energy to make the reaction self-sustaining.

<span class="mw-page-title-main">Fire</span> Rapid and hot oxidation of a material

Fire is the rapid oxidation of a material in the exothermic chemical process of combustion, releasing heat, light, and various reaction products. At a certain point in the combustion reaction, called the ignition point, flames are produced. The flame is the visible portion of the fire. Flames consist primarily of carbon dioxide, water vapor, oxygen and nitrogen. If hot enough, the gases may become ionized to produce plasma. Depending on the substances alight, and any impurities outside, the color of the flame and the fire's intensity will be different.

<span class="mw-page-title-main">Thermite</span> Pyrotechnic composition of metal powder, which serves as fuel, and metal oxide

Thermite is a pyrotechnic composition of metal powder and metal oxide. When ignited by heat or chemical reaction, thermite undergoes an exothermic reduction-oxidation (redox) reaction. Most varieties are not explosive, but can create brief bursts of heat and high temperature in a small area. Its form of action is similar to that of other fuel-oxidizer mixtures, such as black powder.

The autoignition temperature or self-ignition temperature, often called spontaneous ignition temperature or minimum ignition temperature and formerly also known as kindling point, of a substance is the lowest temperature in which it spontaneously ignites in a normal atmosphere without an external source of ignition, such as a flame or spark. This temperature is required to supply the activation energy needed for combustion. The temperature at which a chemical ignites decreases as the pressure is increased.

<span class="mw-page-title-main">Backdraft</span> Rapid or explosive burning of superheated gasses in a fire

A backdraft or backdraught is the abrupt burning of superheated gases in a fire caused when oxygen rapidly enters a hot, oxygen-depleted environment; for example, when a window or door to an enclosed space is opened or broken. Backdrafts are typically seen as a blast of smoke and/or flame out of an opening of a building. Backdrafts present a serious threat to firefighters. There is some debate concerning whether backdrafts should be considered a type of flashover.

A flashover is the near-simultaneous ignition of most of the directly exposed combustible material in an enclosed area. When certain organic materials are heated, they undergo thermal decomposition and release flammable gases. Flashover occurs when the majority of the exposed surfaces in a space are heated to their autoignition temperature and emit flammable gases. Flashover normally occurs at 500 °C (932 °F) or 590 °C (1,100 °F) for ordinary combustibles and an incident heat flux at floor level of 20 kilowatts per square metre (2.5 hp/sq ft).

<span class="mw-page-title-main">Dry distillation</span> Heating of solids to produce gases

Dry distillation is the heating of solid materials to produce gaseous products. The method may involve pyrolysis or thermolysis, or it may not.

<span class="mw-page-title-main">Drying oil</span> Oil that hardens after exposure to air

A drying oil is an oil that hardens to a tough, solid film after a period of exposure to air, at room temperature. The oil hardens through a chemical reaction in which the components crosslink by the action of oxygen. Drying oils are a key component of oil paint and some varnishes. Some commonly used drying oils include linseed oil, tung oil, poppy seed oil, perilla oil, and walnut oil. Their use has declined over the past several decades, as they have been replaced by alkyd resins and other binders.

<span class="mw-page-title-main">Fire triangle</span> Model for understanding the ingredients for fires

The fire triangle or combustion triangle is a simple model for understanding the necessary ingredients for most fires.

<span class="mw-page-title-main">Coal-seam fire</span> Underground smouldering of a coal deposit

A coal-seam fire is a burning of an outcrop or underground coal seam. Most coal-seam fires exhibit smouldering combustion, particularly underground coal-seam fires, because of limited atmospheric oxygen availability. Coal-seam fire instances on Earth date back several million years. Due to thermal insulation and the avoidance of rain/snow extinguishment by the crust, underground coal-seam fires are the most persistent fires on Earth and can burn for thousands of years, like Burning Mountain in Australia. Coal-seam fires can be ignited by self-heating of low-temperature oxidation, lightning, wildfires and even arson. Coal-seam fires have been slowly shaping the lithosphere and changing atmosphere, but this pace has become faster and more extensive in modern times, triggered by mining.

The heating value of a substance, usually a fuel or food, is the amount of heat released during the combustion of a specified amount of it.

<span class="mw-page-title-main">Fire making</span> Process of starting a fire artificially

Fire making, fire lighting or fire craft is the process of artificially starting a fire. It requires completing the fire triangle, usually by heating tinder above its autoignition temperature.

Charring is a chemical process of incomplete combustion of certain solids when subjected to high heat. Heat distillation removes water vapour and volatile organic compounds (syngas) from the matrix. The residual black carbon material is char, as distinguished from the lighter colored ash. By the action of heat, charring removes hydrogen and oxygen from the solid, so that the remaining char is composed primarily of carbon. Polymers like thermoset, or most solid organic compounds like wood or biological tissue, exhibit charring behaviour.

Homogeneous Charge Compression Ignition (HCCI) is a form of internal combustion in which well-mixed fuel and oxidizer are compressed to the point of auto-ignition. As in other forms of combustion, this exothermic reaction produces heat that can be transformed into work in a heat engine.

<span class="mw-page-title-main">Thermal runaway</span> Loss of control of an exothermal process due to temperature increases

Thermal runaway describes a process that is accelerated by increased temperature, in turn releasing energy that further increases temperature. Thermal runaway occurs in situations where an increase in temperature changes the conditions in a way that causes a further increase in temperature, often leading to a destructive result. It is a kind of uncontrolled positive feedback.

<span class="mw-page-title-main">Smouldering</span> Slow, flameless combustion

Smouldering or smoldering is the slow, flameless form of combustion, sustained by the heat evolved when oxygen directly attacks the surface of a condensed-phase fuel. Many solid materials can sustain a smouldering reaction, including coal, cellulose, wood, cotton, tobacco, cannabis, peat, plant litter, humus, synthetic foams, charring polymers including polyurethane foam and some types of dust. Common examples of smouldering phenomena are the initiation of residential fires on upholstered furniture by weak heat sources, and the persistent combustion of biomass behind the flaming front of wildfires.

Pyrolysis oil, sometimes also known as bio-crude or bio-oil, is a synthetic fuel with limited industrial application and under investigation as substitute for petroleum. It is obtained by heating dried biomass without oxygen in a reactor at a temperature of about 500 °C (900 °F) with subsequent cooling, separation from the aqueous phase and other processes. Pyrolysis oil is a kind of tar and normally contains levels of oxygen too high to be considered a pure hydrocarbon. This high oxygen content results in non-volatility, corrosiveness, partial miscibility with fossil fuels, thermal instability, and a tendency to polymerize when exposed to air. As such, it is distinctly different from petroleum products. Removing oxygen from bio-oil or nitrogen from algal bio-oil is known as upgrading.

<span class="mw-page-title-main">Cone calorimeter</span>

A cone calorimeter is an instrument used to study the behavior of fire in small samples of condensed phase materials. It is widely used in the field of fire safety engineering and in oxygen consumption calorimetry.

Flammable solids are any materials in the solid phase of matter that can readily undergo combustion in the presence of a source of ignition under standard circumstances, i.e. without:

Oxygen compatibility is the issue of compatibility of materials for service in high concentrations of oxygen. It is a critical issue in space, aircraft, medical, underwater diving and industrial applications. Aspects include effects of increased oxygen concentration on the ignition and burning of materials and components exposed to these concentrations in service.

References

  1. Babrauskas 2003 , p. 369
  2. Woodward, William T. W. (1 June 2004). "Spontaneous Combustion in Hay Stacks" (PDF). wa-hay.org. Washington State University. Archived from the original (PDF) on 9 May 2008. Retrieved 9 May 2008.
  3. "Fire – Compost and Organic Matter". agric.gov.ab.ca. Government of Alberta. Archived from the original on 11 December 2008. Retrieved 12 January 2009.
  4. Bicevskis, Rob. "Spontaneous Combustion". WildwoodSurvival.com. Archived from the original on 25 February 2020. Retrieved 16 March 2010.
  5. Babrauskas 2003 , pp. 886–890
  6. "The Fire Below: Spontaneous Combustion In Coal (DOE/EH-0320 Issue No. 93-4)". hss.energy.gov. U.S. Department of Energy. May 1993. Archived from the original on 27 May 2010. Retrieved 22 May 2012.
  7. "Pistachio Nuts – RF Self-heating / Spontaneous combustion". tis-gdv.de. The German Insurance Association. Archived from the original on 4 July 2020. Retrieved 5 November 2007.
  8. Bowes 1984 , pp. 376–390
  9. Bowes 1984 , pp. 315–330
  10. Bowes 1984 , pp. 330–333
  11. "Cotton: RF Self-heating / Spontaneous combustion". Transport Information Service: General Association of German Insurers. Archived from the original on 4 March 2009. Retrieved 5 February 2021.
  12. Bowes 1984 , pp. 396–406
  13. Nickell, Joe (December 1996). "Spontaneous Human Nonsense". Skeptical Inquirer . 6 (4). Archived from the original on 9 March 2010.

Bibliography