copyright©2000 by houghton mifflin company. all rights reserved. 1 energy the capacity to do work...
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Copyright©2000 by Houghton Mifflin Company. All rights reserved.
1
EnergyEnergy
The capacity to do work or to produce heat.
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Law of Conservation of Energy
Law of Conservation of Energy
Energy can be converted from one form to another but can neither be created nor destroyed.
(Euniverse is constant)
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The Two Types of EnergyThe Two Types of Energy
Potential: due to position or composition - can be converted to work
Kinetic: due to motion of the object
KE = 1/2 mv2
(m = mass, v = velocity)
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4
Temperature v. HeatTemperature v. Heat
See fig 6.1, p. 242. Note changes in KE/PE Why does B not get as high as A?• Frictional heating: hill gets hotter
Temperature reflects random motions of particles, therefore related to kinetic energy of the system.
Heat involves a transfer of energy between 2 objects due to a temperature difference
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5
Work
• In fig 6.1, B gains PE because work was done on B by A.
• Work: f x d.• So, energy can be transferred two ways:
through work and through heat.• For ball A, PE lost as work or heat depends
on pathway.
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6
State FunctionState Function
Depends only on the present state of the system - not how it arrived there.
It is independent of pathway.
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A note about state functions
• Would you agree that the distance between Chicago and L.A. is fixed?
• This “fixed distance” is analogous to a State Function.
• But the pathway, how we get to L.A. from Chicago, is not fixed.
• Energy is a state function
• Work and Heat are not state functions
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System and SurroundingsSystem and Surroundings
System: That on which we focus attention
Surroundings: Everything else in the universe
Universe = System + Surroundings
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System/Surroundings
• Example:
• CH4 + O2 --> CO2 + 2H2O + heat
• System: the reaction inside your furnace
• Surroundings: everything else (furnace,
house, everything else
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10
Exo and EndothermicExo and Endothermic
Heat exchange accompanies chemical reactions.
Exothermic: Heat flows out of the system (to the surroundings).
Endothermic: Heat flows into the system (from the surroundings).
Where does the the heat come from?
Fig 6.2/6.3 pg 244
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11
Figure 6.2The Combustion of Methane
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Figure 6.3: The Energy Diagram for the Reaction of Nitrogen and Oxygen to Form Nitric Oxide
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First LawFirst Law
First Law of Thermodynamics:
The energy of the universe is constant.
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First LawFirst Law
E = q + w
E = change in system’s internal energy
q = heat
w = work
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Signs
• We always take they systems p.o.v.
• q= + for endothermic ( energy flows
into the system
q = - for exo, (energy flows out system)
w = - (system does work on surr)
w = + (surr do work on the system)
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16
Figure 6.4The Volume of a Cylinder
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PV WorkPV Work
(look at fig 6.4 page 246)
work = force distance, force x h
since P = force / area, (force = P x area)
work = (pressure x area) x h
w = PV expanding gas: work is neg, work done on surr compressed gas: work is pos (V is neg), work done on sys
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18
EnthalpyEnthalpyEnthalpy = H = E + PV
E = H PVH = E + PV
At constant pressure,
E = qP PV or
qP = E + PV,
where qP = H at constant pressure
H = energy flow as heat (at constant pressure)
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19
Change in Enthalpy
• Flow of heat is change in ethalpyH = Hproducts Hreactants
H = neg exothermicH = pos endothermic
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20
Calorimetry
• Science of measuring heat.
• Calorimeter -->• Heat capacity: energy
required to change the temperature of a substance.
• C = heat absorbed (Joules) Increase in temp
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Figure 6.6A Bomb Calorimeter
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Heat CapacityHeat Capacity
C = heat absorbed
increase in temperature =
JC
or JK°
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Heat Exchange Terms Heat Exchange Terms
specific heat capacityheat capacity per gram = J/°C g or J/K g
ex. Water: 4.18 J/ °C g
molar heat capacityheat capacity per mole = J/°C mol or J/K mol
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24
Hess’s LawHess’s Law
Reactants Products
The change in enthalpy is the same whether the reaction takes place in one step or a series of steps.
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Figure 6.7The Principle of Hess’s Law
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Calculations via Hess’s LawCalculations via Hess’s Law
1. If a reaction is reversed, H is also reversed.
N2(g) + O2(g) 2NO(g) H = 180 kJ
2NO(g) N2(g) + O2(g) H = 180 kJ
2. If the coefficients of a reaction are multiplied by an integer, H is multiplied by that same integer.
6NO(g) 3N2(g) + 3O2(g) H = 540 kJ
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Standard StatesStandard States
Compound For a gas, pressure is exactly 1 atmosphere. For a solution, concentration is exactly 1 molar. Pure substance (liquid or solid), it is the pure liquid or
solid.
Element The form [N2(g), K(s)] in which it exists at 1 atm and
25°C.
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28
Change in EnthalpyChange in Enthalpy
Can be calculated from enthalpies of formation of reactants and products.
Hrxn° = npHf(products) nrHf(reactants)
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29
Figure 6.10A Pathway for the Combustion of
Ammonia
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Figure 6.11Energy Sources Used in the
United States
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Petroleum/nat. gas
• From marine organisms 500 my ago• Petroleum: liquid mix of hydrocarbons• Natural Gas: methane, ethane, butane, propane.• Petroleum separated by separated by boiling point.
Table 6.3/6.4• Kerosene the original: replacewhale oil/animal
fats in oil lamps
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Fractional Distillation
QuickTime™ and a decompressor
are needed to see this picture.
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33
Coal
• From plants, dead, buried with heat/pressure. ( 300 my ago)
• Cellulose (CH2O empirical) from plants
slowly becomes more pure in C.
• 300 my ago nothing evolved yet to eat
cellulose.
• Use expected to increase - problems
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34
Figure 6.12The Earth’s Atmosphere
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Figure 6.13Atmospheric CO2 Concentration
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What other energy sources do we have?
• Coal gasification:syngas
AK could benefit
• Hydrogen.
• Oil shale
• Nuclear
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37
Figure 6.14Coal Gasification
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38
Hydrogen
• H2 + .5O2 --> H2O ∆H˚= -286 kJ
• Much greater than methane
• Problems:
production, storage, transport
Production: a. CH4 + H2O --> 3 H2 + CO
∆H˚ = 206 kJ
( b. Decomp water ∆H˚= 286 kJ