Chapter 20. Heat and the First Law of Thermodynamics

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Presentation transcript:

Chapter 20. Heat and the First Law of Thermodynamics

Thermodynamics – Historical Background Thermodynamics and mechanics were considered to be separate branches Until about 1850 Experiments by James Joule and others showed a connection between them A connection was found between the transfer of energy by heat in thermal processes and the transfer of energy by work in mechanical processes The concept of energy was generalized to include internal energy The Law of Conservation of Energy emerged as a universal law of nature

20.1 Internal Energy Internal energy is all the energy of a system that is associated with its microscopic components These components are its atoms and molecules The system is viewed from a reference frame at rest with respect to the center of mass of the system

Internal Energy and Other Energies The kinetic energy due to its motion through space is not included Internal energy does include kinetic energies due to: Random translational motion Rotational motion Vibrational motion Internal energy also includes potential energy between molecules

Heat Heat is defined as the transfer of energy across the boundary of a system due to a temperature difference between the system and its surroundings The term heat will also be used to represent the amount of energy transferred by this method

Changing Internal Energy Both heat and work can change the internal energy of a system The internal energy can be changed even when no energy is transferred by heat, but just by work Example, compressing gas with a piston Energy is transferred by work

Units of Heat Historically, the calorie was the unit used for heat One calorie is the amount of energy transfer necessary to raise the temperature of 1 g of water from 14.5oC to 15.5oC The “Calorie” used for food is actually 1 kilocalorie!! In the US Customary system, the unit is a BTU (British Thermal Unit) One BTU is the amount of energy transfer necessary to raise the temperature of 1 lb of water from 63oF to 64oF The SI units for heat will be: Joules

Mechanical Equivalent of Heat Joule established the equivalence between mechanical energy and internal energy His experimental setup is shown at right The loss in potential energy associated with the blocks equals the work done by the paddle wheel on the water

Mechanical Equivalent of Heat, cont Joule found that it took approximately 4.18 J of mechanical energy to raise the water 1oC Later, more precise, measurements determined the amount of mechanical energy needed to raise the temperature of water from 14.5oC to 15.5oC 1 cal = 4.186 J (20.1) This is known as the mechanical equivalent of heat!!!

20.2 Specific Heat and Calorimetry The heat capacity, C, of a particular sample is defined as the amount of energy (Q) needed to raise the temperature of that sample by 1oC If energy Q produces a change of temperature of DT, then Q = C DT (20.2)  C = Q/DT (20.2a)

Specific Heat Specific heat, c, is the heat capacity per unit mass If energy Q transfers to a sample of a substance of mass m and the temperature changes by DT, then the specific heat is: c = C/m  (20.3)

Specific Heat, cont The specific heat is essentially a measure of how insensitive a substance is to the addition of energy The greater the substance’s specific heat, the more energy that must be added to cause a particular temperature change The equation is often written in terms of Q : Q = mc DT (20.4)

Some Specific Heat Values

Sign Conventions If the temperature increases: Q and DT are POSITIVE Energy transfers INTO the system!!! If the temperature decreases: Q and DT are NEGATIVE Energy transfers OUT of the system!!!

Specific Heat Varies With Temperature Technically, the specific heat varies with temperature The corrected equation is However, if the temperature intervals are not too large, the variation can be ignored and c can be treated as a constant There is only about a 1% variation between 0o and 100oC

Specific Heat of Water Water has the highest specific heat of common materials This is responsible for many weather phenomena Moderate temperatures near large bodies of water Global wind systems Land and sea breezes

Example 20.1 A very Hot Frying Pan Accidentally an empty iron frying pan gets very hot on the stove (~300oC). What happen when you dunk it into a few inches of cool water in the bottom of the sink? Assume: Mwater ≈ Mpan Water warms up (~10oC to 20oC) Water does not come close to boiling. Since: Mwater ≈ Mpan & cwater ~ 10ciron  from heat Q leaving the pan enters the water, and the iron’s pan DT will be 10 times greater than DT of the water. If you let a few drops of water fall onto the hot pan, that very small mass of water will sizzle and boil away since: Mpan ~ 100Mwater

Calorimetry One technique for measuring specific heat involves heating a material, adding it to a sample of water, and recording the final temperature This technique is known as calorimetry A calorimeter is a device in which this energy transfer takes place The system of the sample and the water is isolated Conservation of energy requires that the amount of energy that leaves the sample equals the amount of energy that enters the water

Calorimetry, final Conservation of Energy gives a mathematical expression of this: Qcold= –Qhot (20.5) The negative sign in the equation is critical for consistency with the established sign convention Since each Q = mc DT, csample can be found by: Technically, the mass of the container should be included, but if mw >>mcontainer it can be neglected

Example 20.2 Cooling a Hot Ingot A 0.400kg ingot of metal is heated to 200oC and then dropped into a beaker of water initially at 20oC. The equilibrium temperature is 22.4oC, find specific heat, c of the metal.

20.3 Latent Heat A phase change is when a substance changes from one form to another Two common phase changes are Solid to liquid (melting) Liquid to gas (boiling) During a phase change, THERE IS NO CHANGE in temperature of the substance!!! Different substances react differently to the energy added or removed during a phase change Due to their different molecular arrangements The amount of energy also depends on the mass of the sample

Latent Heat, cont If an amount of energy Q is required to change the phase of a sample of mass m, L = Q /m The quantity L is called the latent heat of the material Latent means “hidden” The value of L depends on the substance as well as the actual phase change The energy required to change the phase is Q = ± mL (20.6)

Latent Heat, final The latent heat of fusion is used when the phase change is from solid to liquid The latent heat of vaporization is used when the phase change is from liquid to gas The positive sign is used when the energy is transferred into the system This will result in melting or boiling The negative sign is used when energy is transferred out of the system This will result in freezing or condensation

Sample Latent Heat Values

Graph of Ice to Steam

Warming Ice, Graph Part A Start with one gram of ice at –30.0ºC During phase A, the temperature of the ice changes from –30.0ºC to 0ºC Use Q = mi ci DT In this case, 62.7 J of energy are added

Melting Ice, Graph Part B Once at 0ºC, the phase change (melting) starts The temperature stays the same although energy is still being added Use Q = mi Lf The energy required is 333 J On the graph, the values move from 62.7 J to 396 J

Warming Water, Graph Part C Between 0ºC and 100ºC, the material is liquid and no phase changes take place Energy added increases the temperature Use Q = mwcw DT 419 J are added The total is now 815 J

Boiling Water, Graph Part D At 100ºC, a phase change occurs (boiling) Temperature does not change Use Q = mw Lv This requires 2260 J The total is now 3070 J

Heating Steam After all the water is converted to steam, the steam will heat up No phase change occurs The added energy goes to increasing the temperature Use Q = mscs DT In this case, 40.2 J are needed The temperature is going to 120o C The total is now 3110 J

Molecular View of Phase Changes Phase changes can be described in terms of the rearrangement of molecules (or atoms in an elemental substance) Liquid to Gas phase change Molecules in a liquid are close together The forces between them are stronger than those in a gas Work must be done to separate the molecules The latent heat of vaporization is the energy per unit mass needed to accomplish this separation

Molecular View of Phase Changes, cont Solid to Liquid phase change The addition of energy will cause the amplitude of the vibration of the molecules about their equilibrium position to increase At the melting point, the amplitude is great enough to break apart bonds between the molecules The molecules can move to new positions The molecules in the liquid are bound together less strongly than those of the solid The latent heat of fusion is the energy per unit mass required to go from the solid-type to the liquid-type bonds

Molecular View of Phase Changes, final The latent heat of vaporization is greater than the latent heat of fusion In the liquid-to-gas phase change, the liquid-type bonds are broken The gas molecules are essentially not bonded to each other It takes more energy to completely break the bonds than to change the type of bonds

Calorimetry Problem-Solving Strategy Units of measure must be consistent For example, if your value of c is in J/kg.oC, then your mass must be in kg, the temperatures in oC and energies in J Transfers of energy are given by Q =mc DT only when no phase change occurs If there is a phase change, use Q = mL Be sure to select the correct sign for all energy transfers Remember to use Qcold = –Qhot The DT is always Tf - Ti

Example 20.3 Cooling the Steam What mass of steam initially at 130oC is needed to warm 200-g of water in a 100-g glass container from 20oC to 50.0oC Steam loses energy in 3 stages: 1st stage: Steam  100oC , DT = –30oC 2nd stage: Steam  water 3rd stage: Water  50oC , DT = –50oC

Example 20.3 Cooling the Steam, final Adding the energy transfer in the 3 stages: Water and Glass increasing temperature: DT = 30oC Final: Qcold = –Qhot

Material for the Final Exam Examples to Read!!! Example 20.1 (page 607) Example 20.3 (page 610) Homework to be solved in Class!!! Questions: 2, 12 Problems: 4, 15