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enthalpy and condensation
An alternative description is to view the enthalpy of condensation as the heat which must be released to the surroundings to compensate for the drop in entropy when a gas condenses to a liquid.
The large value of the enthalpy of condensation of water vapour is the reason that steam is a far more effective heating medium than boiling water, and is more hazardous.

enthalpy and heat
Assuming thermal equilibrium between the anode surface and the transpiring argon, the gas enthalpy rise through the anode was calculated according to the relation Af whereby the specific heat of argon was taken as Af.
Using the Debye model, the specific heat and entropy of a pure crystal are proportional to T < sup > 3 </ sup >, while the enthalpy and chemical potential are proportional to T < sup > 4 </ sup >.
( The heat change at constant pressure is called the enthalpy change ; in this case the enthalpy of formation ).
In chemistry, the letter H as symbol of enthalpy sometimes is said to be a Greek eta, but since enthalpy comes from ἐνθάλπος, which begins in a smooth breathing and epsilon, it is more likely a Latin H for ' heat '.
This means that the change in enthalpy under such conditions is the heat absorbed ( or released ) by a chemical reaction.
The word enthalpy is based on the Greek word enthalpos ( ἔνθαλπος ), which means to put heat into.
In order to discuss the relation between the enthalpy increase and heat supply we return to the first law for closed systems: dU
From this relation we see that the increase in enthalpy of a system is equal to the added heat
For systems at constant pressure, the change in enthalpy is the heat received by the system.
If ΔH is positive, the reaction is endothermic, that is heat is absorbed by the system due to the products of the reaction having a greater enthalpy than the reactants.
On the other hand if ΔH is negative, the reaction is exothermic, that is the overall decrease in enthalpy is achieved by the generation of heat.
Fig. 1 During Steady-state ( chemical engineering ) | steady, continuous operation, an energy balance applied to an open system equates shaft work performed by the system to heat added plus net enthalpy added
Helium-3 has a negative enthalpy of fusion at temperatures below 0. 3 K. Helium-4 also has a very slightly negative enthalpy of fusion below 0. 8 K. This means that, at appropriate constant pressures, heat must be removed from these substances in order to melt them.
The heat energy, or enthalpy, associated with a solid to liquid transition is the enthalpy of fusion and that associated with a solid to gas transition is the enthalpy of sublimation.
The subject commonly includes calculations of such quantities as heat capacity, heat of combustion, heat of formation, enthalpy, entropy, free energy, and calories.
The enthalpy of vaporization, ( symbol ), also known as the heat of vaporization or heat of evaporation, is the energy required to transform a given quantity of a substance from a liquid into a gas at a given pressure ( often atmospheric pressure ).
Values are usually quoted in J / mol or kJ / mol ( molar enthalpy of vaporization ), although kJ / kg or J / g ( specific heat of vaporization ), and older units like kcal / mol, cal / g and Btu / lb are sometimes still used, among others.

enthalpy and is
This calculation results in an enthalpy rise which is somewhat high because it assumes a mass flow equally distributed over the plug cross section whereas in reality the mass velocity is expected to be smaller in the regions of higher temperatures.
Since the relation between changes in Gibbs free energy ( G ), the enthalpy ( H ) and the entropy is
Above, h is enthalpy, k is the thermal conductivity of the fluid, T is temperature, and is the viscous dissipation function.
Enthalpy of dissolution in hydrochloric acid at standard conditions is − 600 kJ / mol < sup >− 1 </ sup >, from which the standard enthalpy change of formation ( Δ < sub > f </ sub > H °) of aqueous Bk < sup > 3 +</ sup > ions is obtained as − 601 kJ / mol < sup >− 1 </ sup >.
In thermochemistry, an element is defined to have an enthalpy of formation of zero in its standard state.
A particularly important objective, called computational thermochemistry, is to calculate thermochemical quantities such as the enthalpy of formation to chemical accuracy.
The associated free energy of the reaction is composed of two different thermodynamic quantities, enthalpy and entropy:
The unit of measurement for enthalpy in the International System of Units ( SI ) is the joule, but other historical, conventional units are still in use, such as the British thermal unit and the calorie.
The enthalpy is the preferred expression of system energy changes in many chemical, biological, and physical measurements, because it simplifies certain descriptions of energy transfer.
This is because a change in enthalpy takes account of energy transferred to the environment through the expansion of the system under study.
Thus, change in enthalpy, ΔH, is a more useful quantity than its absolute value.
The word enthalpy is often incorrectly attributed to Benoit Paul Émile Clapeyron and Rudolf Clausius through the 1850 publication of their Clausius-Clapeyron relation.

enthalpy and by
This transition occurs without change in volume, but the enthalpy increases by 3. 66 kJ / mol.
Instead, the word " enthalpy " first appears in the scientific literature in a 1909 publication by J. P. Dalton.
In thermodynamics, one can calculate enthalpy by determining the requirements for creating a system from " nothingness "; the mechanical work required, pV, differs based upon the constancy of conditions present at the creation of the thermodynamic system.
This process is calculated within enthalpy calculations as U + pV, to label the amount of energy or work required to " set aside space for " and " create " the system ; describing the work done by both the reaction or formation of systems, and the surroundings.
In a similar manner, for an endothermic reaction, the system's change in enthalpy is equal to the energy absorbed in the reaction, including the energy lost by the system and gained from compression from its surroundings.
On the other hand, the molecules in liquid water are held together by relatively strong hydrogen bonds, and its enthalpy of vaporization, 40. 65 kJ / mol, is more than five times the energy required to heat the same quantity of water from 0 ° C to 100 ° C ( c < sub > p </ sub > = 75. 3 J K < sup >− 1 </ sup > mol < sup >− 1 </ sup >).
Dividing the energy change by how many moles of A were present gives its enthalpy change of reaction.
This means that the change in enthalpy minus the change in entropy ( multiplied by the absolute temperature ) is a negative value, or that the Gibbs free energy of the system decreases.

enthalpy and definition
The definition of enthalpy, H, permits us to use this thermodynamic potential to account for both internal energy and pV work in fluids for open systems:
by definition the enthalpy change has a negative value:
Another definition, used by Gas Processors Suppliers Association ( GPSA ) and originally used by API ( data collected for API research project 44 ), is the enthalpy of all combustion products minus the enthalpy of the fuel at the reference temperature ( API research project 44 used 25 ° C.
Using the definition of specific enthalpy, and the fact that the temperature and pressure are constant, we have

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