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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. [1]
The instrument gathers data about the ignition time, mass loss, combustion products, heat release rate, and other parameters associated with the sample's burning properties. The measurement of the heat release rate is based on Huggett's principle [2] that the gross heat of combustion of any organic material is directly related to the amount of oxygen required for combustion. Its name comes from the conical shape of a radiant heater incorporated into the instrument that can produce a nearly uniform heat flux over the surface of the sample under study. [3]
In the 1960s, researchers at the National Institute of Standards and Technology (NIST) determined that the heat release from a fire directly related to the growth rate of a fire and was thus a major factor in the fire's risk to life and property. However, prior devices used to measure heat release typically estimated the heat release of a fire by measuring the increase in temperature of ambient air flowing past the combusting material and these measurements of heat release were often inaccurate, so a more reliable device was desired. [4]
Through the 1960s and 1970s, research efforts developed a more accurate method for estimating heat release. In 1977, William Parker published research that demonstrated that heat release during combustion was roughly constant per unit of oxygen consumed for a variety of fuels. By measuring the oxygen consumed during combustion, one could estimate heat release of a fire; this method is now termed oxygen consumption calorimetry. [5] This finding was a rediscovery of a method first identified in 1917 by W. M. Thornston, whose research similarly found that during combustion of organic liquids and gases, a consistent amount of heat was released per unit mass of oxygen consumed. [6] Clayton Huggett later provided a rigorous proof of concept in his 1980 paper to suggest oxygen consumption calorimetry was a significantly more accurate method for estimating heat release than prior methods. [2]
Following the development of oxygen consumption calorimetry, in 1982, Vytenis Babrauskas and colleagues at the Center for Fire Research built the first cone calorimeter. [7] The cone calorimeter was quickly realized as an important instrument for modern fire safety tests, being formally recognized in 1988 by an R&D 100 Award. [8] The cone calorimeter is used today for both regulatory and research purposes. [3]
The cone calorimeter is used in several standard models to evaluate different aspects of flammable materials. As a reduced-scale apparatus, the size of the instrument typically limits the size of samples to less than 100 mm2. [1] Compared to previous devices used in calorimetry, the cone calorimeter produces more reliable data, but must be scaled up to reflect actual fire safety considerations. [4]
The instrument is used by encasing a small sample in aluminium foil, wool, and a retainer frame that is ignited below an exhaust hood. A conical heater is placed in between in order for materials to combust. The cone-shaped Inconel heating element provides a controllable radiant flux onto the sample, turning electricity into heat not unlike an electric toaster or oven. The flammability of a sample can be characterized as a function of heat flux onto a sample. The conical heater is open in its center, allowing products of combustion to flow upwards into an exhaust duct. Soot can be collected in the bottom of the frame for gravimetric analysis.
Ventilation is also a very important part of the device, as well as the electrical power to run the conical heater. A small water supply is necessary to cool and regulate the heat in the system of the device. Since temperature and pressure are being evaluated, two different measurement tools are needed in the exhaust tube. Gas samples, smoke measurements, and soot collections are also acquired using this device.
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. The study of combustion is known as combustion science.
In chemistry and thermodynamics, calorimetry is the science or act of measuring changes in state variables of a body for the purpose of deriving the heat transfer associated with changes of its state due, for example, to chemical reactions, physical changes, or phase transitions under specified constraints. Calorimetry is performed with a calorimeter. Scottish physician and scientist Joseph Black, who was the first to recognize the distinction between heat and temperature, is said to be the founder of the science of calorimetry.
The National Institute of Standards and Technology (NIST) is an agency of the United States Department of Commerce whose mission is to promote American innovation and industrial competitiveness. NIST's activities are organized into physical science laboratory programs that include nanoscale science and technology, engineering, information technology, neutron research, material measurement, and physical measurement. From 1901 to 1988, the agency was named the National Bureau of Standards.
Thermochemistry is the study of the heat energy which is associated with chemical reactions and/or phase changes such as melting and boiling. A reaction may release or absorb energy, and a phase change may do the same. Thermochemistry focuses on the energy exchange between a system and its surroundings in the form of heat. Thermochemistry is useful in predicting reactant and product quantities throughout the course of a given reaction. In combination with entropy determinations, it is also used to predict whether a reaction is spontaneous or non-spontaneous, favorable or unfavorable.
A calorimeter is a device used for calorimetry, or the process of measuring the heat of chemical reactions or physical changes as well as heat capacity. Differential scanning calorimeters, isothermal micro calorimeters, titration calorimeters and accelerated rate calorimeters are among the most common types. A simple calorimeter just consists of a thermometer attached to a metal container full of water suspended above a combustion chamber. It is one of the measurement devices used in the study of thermodynamics, chemistry, and biochemistry.
Differential scanning calorimetry (DSC) is a thermoanalytical technique in which the difference in the amount of heat required to increase the temperature of a sample and reference is measured as a function of temperature. Both the sample and reference are maintained at nearly the same temperature throughout the experiment. Generally, the temperature program for a DSC analysis is designed such that the sample holder temperature increases linearly as a function of time. The reference sample should have a well-defined heat capacity over the range of temperatures to be scanned. Additionally, the reference sample must be stable, of high purity, and must not experience much change across the temperature scan. Typically, reference standards have been metals such as indium, tin, bismuth, and lead, but other standards such as polyethylene and fatty acids have been proposed to study polymers and organic compounds, respectively.
The flash point of a material is the "lowest liquid temperature at which, under certain standardized conditions, a liquid gives off vapours in a quantity such as to be capable of forming an ignitable vapour/air mixture".
In thermochemistry, an exothermic reaction is a "reaction for which the overall standard enthalpy change ΔH⚬ is negative." Exothermic reactions usually release heat. The term is often confused with exergonic reaction, which IUPAC defines as "... a reaction for which the overall standard Gibbs energy change ΔG⚬ is negative." A strongly exothermic reaction will usually also be exergonic because ΔH⚬ makes a major contribution to ΔG⚬. Most of the spectacular chemical reactions that are demonstrated in classrooms are exothermic and exergonic. The opposite is an endothermic reaction, which usually takes up heat and is driven by an entropy increase in the system.
A diamond anvil cell (DAC) is a high-pressure device used in geology, engineering, and materials science experiments. It permits the compression of a small (sub-millimeter-sized) piece of material to extreme pressures, typically up to around 100–200 gigapascals, although it is possible to achieve pressures up to 770 gigapascals.
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.
The wattmeter is an instrument for measuring the electric active power in watts of any given circuit. Electromagnetic wattmeters are used for measurement of utility frequency and audio frequency power; other types are required for radio frequency measurements.
A space heater is a device used to heat a single, small- to medium-sized area. This type of heater can be contrasted with central heating, which distributes heat to multiple areas.
A reaction calorimeter is a calorimeter that measures the amount of energy released or absorbed by a chemical reaction. It does this by measuring the heat change of water stored in a vessel.
A fire test is a means of determining whether fire protection products meet minimum performance criteria as set out in a building code or other applicable legislation. Successful tests in laboratories holding national accreditation for testing and certification result in the issuance of a certification listing.
Spontaneous combustion or spontaneous ignition is a type of combustion which occurs by self-heating, followed by thermal runaway and finally, autoignition. It is distinct from pyrophoricity, in which a compound needs no self-heat to ignite. The correct storage of spontaneously combustible materials is extremely important considering improper storage is the main cause of spontaneous combustion. Materials such as coal, cotton, hay, and oils should be stored at proper temperatures and moisture levels to prevent spontaneous combustion.
Fire-safe polymers are polymers that are resistant to degradation at high temperatures. There is need for fire-resistant polymers in the construction of small, enclosed spaces such as skyscrapers, boats, and airplane cabins. In these tight spaces, ability to escape in the event of a fire is compromised, increasing fire risk. In fact, some studies report that about 20% of victims of airplane crashes are killed not by the crash itself but by ensuing fires. Fire-safe polymers also find application as adhesives in aerospace materials, insulation for electronics, and in military materials such as canvas tenting.
Isothermal microcalorimetry (IMC) is a laboratory method for real-time monitoring and dynamic analysis of chemical, physical and biological processes. Over a period of hours or days, IMC determines the onset, rate, extent and energetics of such processes for specimens in small ampoules at a constant set temperature.
Indirect calorimetry calculates heat that living organisms produce by measuring either their production of carbon dioxide and nitrogen waste, or from their consumption of oxygen. Indirect calorimetry estimates the type and rate of substrate utilization and energy metabolism in vivo starting from gas exchange measurements. This technique provides unique information, is noninvasive, and can be advantageously combined with other experimental methods to investigate numerous aspects of nutrient assimilation, thermogenesis, the energetics of physical exercise, and the pathogenesis of metabolic diseases.
Isotopic reference materials are compounds with well-defined isotopic compositions and are the ultimate sources of accuracy in mass spectrometric measurements of isotope ratios. Isotopic references are used because mass spectrometers are highly fractionating. As a result, the isotopic ratio that the instrument measures can be very different from that in the sample's measurement. Moreover, the degree of instrument fractionation changes during measurement, often on a timescale shorter than the measurement's duration, and can depend on the characteristics of the sample itself. By measuring a material of known isotopic composition, fractionation within the mass spectrometer can be removed during post-measurement data processing. Without isotope references, measurements by mass spectrometry would be much less accurate and could not be used in comparisons across different analytical facilities. Due to their critical role in measuring isotope ratios, and in part, due to historical legacy, isotopic reference materials define the scales on which isotope ratios are reported in the peer-reviewed scientific literature.