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(Redirected from Adiabatic cooling) An adiabatic process is any process occurring without gain or loss of heat within a system (i.e. during the process the system is thermodynamically isolated- there is no heat transfer with the surroundings). This is the opposite of a diabatic process, where there is heat transfer. A key concept in thermodynamics, many rapid chemical and physical processes are described or approximated in this way. Such processes are usually followed or preceded by events that do involve heat transfer (i.e. are non-adiabatic). Examples include electron-transfer. Adiabatic processes can occur if the container of the system has thermally-insulated walls or the process happens in an extremely short time, so that there is no opportunity for significant heat exchange.[1] Although the terms adiabatic and isocaloric can often be interchanged, adiabatic processes may be considered a subset of isocaloric processes; the remaining complement subset of isocaloric processes being processes where net heat transfer does not diverge locally such as in an idealized case with mediums of infinite thermal conductivity or non-existent thermal capacity. For example, an adiabatic boundary is a boundary that is impermeable to heat transfer and the system is said to be diabatically (or thermally) insulated; an insulated wall approximates an adiabatic boundary. Another example is the adiabatic flame temperature, which is the temperature that would be achieved by a flame in the absence of heat loss to the surroundings. An adiabatic process may be described by the statement where is the energy transferred by heating (or cooling). Since, by the second law of thermodynamics, for a reversible process (where T is temperature and S is entropy), a reversible adiabatic process is also an isentropic process ( ). However, for an so that an irreversible adiabatic process is not isentropic. In particular, an adiabatic process that is irreversible and extracts no work (e.g. irreversible process, viscous drag) is in an isenthalpic process, in which entropy increases. One opposite extremeallowing heat transfer with the surroundings, causing the temperature to remain constantis known as an isothermal process. Since temperature is thermodynamically conjugate to entropy, the isothermal process is conjugate to the isentropic process, and therefore to a reversible adiabatic process. A transformation of a thermodynamic system can be considered adiabatic when it is quick enough that no significant heat is transferred between the system and the outside. At the opposite extreme, a transformation of a thermodynamic system can be considered isothermal if it is slow enough so that the system's temperature remains constant by heat exchange with the outside. The term "adiabatic" literally means impassable,[2] coming from the Greek roots - ("not"), - ("through"), and ("to pass"); this etymology corresponds here to an absence of heat transfer.
Contents
1 Adiabatic heating and cooling 2 Ideal gas (reversible process) 2.1 Example of adiabatic compression 2.2 Adiabatic free expansion of a gas 2.3 Derivation of continuous formula for adiabatic heating and cooling 2.4 Derivation of discrete formula 3 Graphing adiabats 4 See also 5 References 6 External links
being the specific heat for constant pressure, being the specific heat for constant volume, is the adiabatic index, and is the number of degrees of freedom (3 for monatomic gas, 5 for diatomic gas and collinear molecules e.g. carbon dioxide). For a monatomic ideal gas, , and for a diatomic gas (such as nitrogen and oxygen, the main components of air) .[4] Note that the above formula is only applicable to classical ideal gases and not BoseEinstein or Fermi gases. For reversible adiabatic processes, it is also true that
For a simple substance, during an adiabatic process in which the volume increases, the internal energy of the working substance must decrease
so our adiabatic constant for this experiment is about 1.58 billion. The gas is now compressed to a 100cc volume (we will assume this happens quickly enough that no heat can enter or leave the gas). The new volume is 100 ccs, but the constant for this experiment is still 1.58 billion:
so solving for P:
or about 362 PSI or 24.5 atm. Note that this pressure increase is more than a simple 10:1 compression ratio would indicate; this is because the gas is not only compressed, but the work done to compress the gas has also heated the gas and the hotter gas will have a greater pressure even if the volume had not changed. We can solve for the temperature of the compressed gas in the engine cylinder as well, using the ideal gas law. Our initial conditions are 100,000 pa of pressure, 1000 cc volume, and 300 K of temperature, so our experimental constant is:
We know the compressed gas has V = 100 cc and P = 2.50E6 pascals, so we can solve for temperature by simple algebra:
That's a final temperature of 751 K, or 477 C, or 892 F, well above the ignition point of many fuels. This is why a high compression engine requires fuels specially formulated to not self-ignite (which would cause engine knocking when operated under these conditions of temperature and pressure), or that a supercharger and intercooler to provide a lower temperature at the same pressure would be advantageous. A diesel engine operates under even more extreme conditions, with compression ratios of 20:1 or more being typical, in order to provide a very high gas temperature which ensures immediate ignition of injected fuel.
where dU is the change in the internal energy of the system and W is work done by the system. Any work (W) done must be done at the expense of internal energy U, since no heat Q is being supplied from the surroundings. Pressure-volume work W done by the system is defined as
However, P does not remain constant during an adiabatic process but instead changes along with V. It is desired to know how the values of dP and dV relate to each other as the adiabatic process proceeds. For an ideal gas the internal energy is given by
where
is the number of degrees of freedom divided by two, R is the universal gas constant and n is the number of moles in the system (a constant). , yields
because
Now substitute equations (2) and (4) into equation (1) to obtain
simplify:
to V and from
Therefore,
and
At the same time, the work done by the pressure-volume changes as a result from this process, is equal to
Since we require the process to be adiabatic, the following equation needs to be true
Integrating,
Substituting
Rearranging,
Using the ideal gas law and assuming a constant molar quantity (as often happens in practical cases),
Or,
Simplifying,
Simplifying,
Simplifying,
Graphing adiabats
An adiabat is a curve of constant entropy on the P-V diagram. Properties of adiabats on a P-V diagram are: 1. 2. 3. 4. 5. Every adiabat asymptotically approaches both the V axis and the P axis (just like isotherms). Each adiabat intersects each isotherm exactly once. An adiabat looks similar to an isotherm, except that during an expansion, an adiabat loses more pressure than an isotherm, so it has a steeper inclination (more vertical). If isotherms are concave towards the "north-east" direction (45 ), then adiabats are concave towards the "east north-east" (31 ). If adiabats and isotherms are graphed severally at regular changes of entropy and temperature, respectively (like altitude on a contour map), then as the eye moves towards the axes (towards the south-west), it sees the density of isotherms stay constant, but it sees the density of adiabats grow. The exception is very near absolute zero, where the density of adiabats drops sharply and they become rare (see Nernst's theorem).
The following diagram is a P-V diagram with a superposition of adiabats and isotherms:
The isotherms are the red curves and the adiabats are the black curves. The adiabats are isentropic. Volume is the horizontal axis and pressure is the vertical axis.
See also
Cyclic process First law of thermodynamics Heat burst Isobaric process Isenthalpic process Isentropic process Isochoric process Isothermal process Polytropic process Entropy (classical thermodynamics) Quasistatic equilibrium Total air temperature Adiabatic engine Magnetic refrigeration
References
1. ^ http://buphy.bu.edu/~duffy/semester1/c27_process_adiabatic_sim.html 2. ^ http://dictionary.reference.com/browse/adiabatic 3. ^ Kavanagh, J.L.; Sparks R.S.J. (2009). "Temperature changes in ascending kimberlite magmas" (http://monash.academia.edu/JanineKavanagh/Papers/114092/Temperature_ changes_in_ascending_kimberlite_magma). Earth and Planetary Science Letters (Elsevier) 286 (34): 404413. Bibcode:2009E&PSL.286..404K (http://adsabs.harvard.edu/abs/2009E %26PSL.286..404K). doi:10.1016/j.epsl.2009.07.011 (http://dx.doi.org/10.1016% 2Fj.epsl.2009.07.011). Retrieved 18 February 2012. 4. ^ Adiabatic Processes (http://hyperphysics.phy-astr.gsu.edu/hbase/thermo/adiab.html)
Silbey, Robert J.; et al. (2004). Physical chemistry. Hoboken: Wiley. p. 55. ISBN 978-0-471-21504-2. Broholm, Collin. "Adiabatic free expansion." Physics & Astronomy @ Johns Hopkins University. N.p., 26 Nov. 1997. Web. 14 Apr. *Nave, Carl Rod. "Adiabatic Processes." HyperPhysics. N.p., n.d. Web. 14 Apr. 2011. <http://hyperphysics.phy-astr.gsu.edu/hbase/thermo/adiab.html>. Thorngren, Dr. Jane R.. "Adiabatic Processes." Daphne A Palomar College Web Server. N.p., 21 July 1995. Web. 14 Apr. 2011. <http://daphne.palomar.edu/ jthorngren/adiabatic_processes.htm>.
External links
Article in HyperPhysics Encyclopaedia (http://hyperphysics.phy-astr.gsu.edu/hbase/thermo/adiab.html#c1:) Retrieved from "http://en.wikipedia.org/w/index.php?title=Adiabatic_process&oldid=547353379#Adiabatic_heating_and_cooling" Categories: Thermodynamic processes Atmospheric thermodynamics This page was last modified on 28 March 2013 at 00:07. Text is available under the Creative Commons Attribution-ShareAlike License; additional terms may apply. By using this site, you agree to the Terms of Use and Privacy Policy. Wikipedia is a registered trademark of the Wikimedia Foundation, Inc., a non-profit organization.