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ME 20000THERMODYNAMICS 1 SPRING 2020 SECTIONS 1.1–3.15
Riley BartaPerry Teaching Fellow
1
DO YOU KNOW YOUR UNITS?
2
VITAL TO OBTAINING ALL POINTS, CAN HELP CHECK EQUATION USE
Pressure
• 1 bar = 0.1 MPa = 100 kPa = 105 Pa
Temperature:
• T(K) = T(℃) + 273.15
• ΔT K = ΔT(℃)
Force:
• 1 N = 1 kg × 1 m/s2
Energy:
• 1 J = 1 N × m = 1 Pa × 1 m3
Power:
• 1 W = 1 J/s, 1 kW = 103 W
BASIC CONCEPTS
3
What are the types of systems?
What is a property?
What are the types of properties?
What is state?
What is state principle?
ENERGY INTERACTIONS
4
ENERGY INTERACTIONS
(CONT’D)Closed system energy balance (i.e. for piston-cylinder, rigid tanks, etc.)
𝑊 includes boundary work plus any other work interactions (electrical
work, shaft work, spring work, etc.)
Δ𝐸 = Δ𝑈 + Δ𝐾𝐸 + Δ𝑃𝐸 = 𝑄 −𝑊
Sign Conventions:
W > 0 (positive) work done by the system (work output)
W < 0 (negative) work done on the system (work input)
Q > 0 (positive) heat transfer into system (heat input)
Q < 0 (negative) heat transfer out of system (heat output)
PROPERTY DETERMINATION
5
ENERGY INTERACTIONS
(CONT’D)
Look for two independent intensive properties to fix the state of the pure
substance
1.) Start in either saturated temperature or saturated pressure table to
determine the phase
2.) Determine the phase as saturated liquid (SL), saturated liquid-vapor
mixture (SLVM), saturated vapor (SV), compressed liquid (CL), or
superheated vapor (SHV)
3.) Based on Step 2, use appropriate set of tables to fix the state of the
pure substance
Which previously independent, intensive properties become dependent
on/in the dome?
PROPERTY DETERMINATION
6
ENERGY INTERACTIONS
(CONT’D)
Known properties: 𝑇, 𝑣 , or 𝑇, 𝑢 , or 𝑇, ℎ OR 𝑃, 𝑣 , or 𝑃, 𝑢 , or 𝑃, ℎ
IF: 𝑣 > 𝑣𝑔, or 𝑢 > 𝑢𝑔, or ℎ > ℎ𝑔 at the given 𝑇 or 𝑃, then the state is SHV.
We must use an appropriate superheated vapor table.
IF: 𝑣𝑓 < 𝑣 < 𝑣𝑔, or 𝑢𝑓 < 𝑢 < 𝑢𝑔, or ℎ𝑓 < ℎ < ℎ𝑔 at the given 𝑇 or 𝑃, then the
state is SLVM. We must compute quality 𝑥 , and use quality to compute
other properties.
IF: 𝑣 < 𝑣𝑓, or 𝑢 < 𝑢𝑓, or ℎ < ℎ𝑓 at the given 𝑇 or 𝑃, then the state is CL. We
must use an appropriate compressed liquid table, if we can find one.
CL approximation:
𝑥 =𝑣 − 𝑣𝑓
𝑣𝑔 − 𝑣𝑓=
𝑢 − 𝑢𝑓
𝑢𝑔 − 𝑢𝑓=
ℎ − ℎ𝑓
ℎ𝑔 − ℎ𝑓≡
𝑚𝑔
𝑚𝑓 +𝑚𝑔
PHASE CHANGE – T-𝒗 DIAGRAM
7
ENERGY INTERACTIONS
(CONT’D)
Critical
point
𝑣
𝑇 𝑃1
𝑃2 > 𝑃1
𝑇𝑐
𝑃𝑐Sat. Vapor line
Sat. Liquid line
CL
states
SHV
statesSLVM
states
𝑃0 < 𝑃1
Sat. vapor at 𝑃0
Sat. liquid at 𝑃0
Line of constant
pressure
PHASE CHANGE – P-𝒗 DIAGRAM
8
ENERGY INTERACTIONS
(CONT’D)
𝑣
𝑃𝑐𝑇𝑐
Sat. Vapor line
Sat. Liquid line
CL
state
s
SHV
statesSLVM
states𝑃
Critical
point
𝑇1𝑇2 > 𝑇1
𝑇0 < 𝑇1
Line of constant
temp
SPECIFIC HEATS
9
Heat (energy) required to rise the temperature of a unit mass of a
substance by one degree.
Two types of specific heats:
• Specific heat at constant volume 𝑐𝑣
• Specific heat at constant pressure 𝑐𝑝
Specific heat at constant volume (𝒄𝒗)
Specific heat at constant pressure (𝒄𝒑)
𝑐𝑣 =𝜕𝑢
𝜕𝑇𝑣
𝑐𝑝 =𝜕ℎ
𝜕𝑇𝑝
INCOMPRESSIBLE SUBSTANCES
10
Substances where volume changes associated with pressure changes
are negligible.
Can be a valid assumption for liquids and solids, but not gases
𝑐𝑝 = 𝑐𝑣 = 𝑐
If we assume constant specific heats:
𝑢2 − 𝑢1 = 𝑐 𝑇2 − 𝑇1
ℎ2 − ℎ1 = 𝑐 𝑇2 − 𝑇1 + 𝑣 𝑃2 − 𝑃1
IDEAL GAS ASSUMPTION
11
When can we model a substance as an ideal gas?
What is the difference between ideal gas and superheated vapor phase?
What is the ideal gas equation of state?
What single, intensive property can we use to determine other properties
with an ideal gas?
IDEAL GAS ASSUMPTION
12
𝑅: specific gas constant 𝑅 =ത𝑅
𝑀, 𝑀 = molecular weight (kg/mol)
𝑃𝑣 = 𝑅𝑇
USE ABOLUSTE PRESSURE
AND TEMPERATURE – Pascals
(Pa) and Kelvin (K)
• ത𝑅 is the universal gas contant, ത𝑅 = 8.314kJ
kmol−K
𝑃𝑉 = 𝑚𝑅𝑇
𝑐𝑝 = 𝑐𝑣 + 𝑅 𝑐𝑣 =𝑅
𝑘 − 1 𝑐𝑝 =𝑘𝑅
𝑘 − 1
• Specific heat ratio, 𝑘 = 𝑐𝑝/𝑐𝑣 Always greater than 1!
• 𝑐𝑝 and 𝑐𝑣 can be expressed in terms of 𝑘 and 𝑅 for ideal
gases
IDEAL GAS ASSUMPTION
13
IDEAL GAS MODEL (CONT’D)• Use tabulated data: most accurate, ideal gas tables
• Use constant specific heats: note that 𝑐𝑣 ≠ 𝑐𝑝 for ideal gases
Δ𝑢 = 𝑢2(𝑇2) − 𝑢1(𝑇1)
Δℎ = ℎ2(𝑇2) − ℎ1(𝑇1)
values at 𝑻𝟏 and 𝑻𝟐 from ideal
gas tables
Δ𝑢 ≈ 𝑐𝑣(𝑇2 − 𝑇1)
Δℎ ≈ 𝑐𝑝(𝑇2 − 𝑇1)
Only when 𝒄𝒗 and 𝒄𝒑 are
constant or almost constant
for the temperature range
Computing changes in 𝑢 and ℎ for ideal gases
COMMON ELEMENTS
14
FROM ALL SPECIAL PROBLEMS AND SOLVED EXAMPLES THUS FAR
Assumptions:
1. Closed system
2. Quasi-equilibrium process
3. Frictionless piston
4. ∆KE ≈ ∆PE ≈ 0
5. …
Basic equations:
1.
2. → special case: cycles
3.
4.
5. …
W pdV E KE PE U Q W
,V m U mu
,f g f f g fx u u x u u
BOUNDARY WORK
15
MATCH CORRECT TERMS
Process Path Work equation
Isobaric
Isochoric
Product of pressure and
volume remains constant
Polytropic
W p V
0W
2 2 1 1
1
p V p VW
n
21 1
1
lnV
W p VV
𝑃 = 𝐶𝑜𝑛𝑠𝑡𝑎𝑛𝑡
𝑉 = 𝐶𝑜𝑛𝑠𝑡𝑎𝑛𝑡
𝑃𝑉𝑛 = 𝐶𝑜𝑛𝑠𝑡𝑎𝑛𝑡
𝑃𝑉 = 𝐶𝑜𝑛𝑠𝑡𝑎𝑛𝑡
WORK
16
• Remember to include all kinds of work done in the energy balance:
•
• Shaft does work on system, system does boundary work
100 kPaatmp
boundary shaftW W W
2
1
V
boundary
V
W pdV
2
1
shaftW d
EXAMPLE 1
17
DRAW P-V DIAGRAM 100 kPaatmp 100 kPaatmp
1 120 kPap 2 ?p
2
4000 N
0.2 m
weightpiston
A
p
V
atmp
1 2p p
mg
A
1V2V
1 2p p
Q
EXAMPLE 2
18
DRAW P-V DIAGRAM 100 kPaatmp
3 200 kPap
2
4000 N
0.2 m
weightpiston
A
Which additional
assumption is
needed here?
Hint: related to
gas mass
atmp
mg
A3p
R
p
V
1 ?p
2 3V V1V
1 2p p
3p
Q
EXAMPLE 3
19
DRAW P-V DIAGRAM 100 kPaatmp
2 160 kPap 2
4000 N
0.2 m
weightpiston
A
1 80 kPap
Which additional
assumption is
needed here?
Hint: related to
gas mass
2 0k x x
A
mg
A2p
atmp
p
V1V 2V
1p
2p
Q
EXAMPLE 4
20
DRAW P-V DIAGRAM 100 kPaatmp
1 100 kPap 2 ?p
rigid tank
p
V
1p
1 2V V
2p
Would pressure
measured at the
top face and
bottom face of
the tank be the
same?
Q
PROBLEM 1A
21
• 100 kg of water at 10 bar and 179.9 ℃ fills up a rigid tank. What is
the volume of the tank?
a) 0.1127 m3
b) 194.4 m3
c) Insufficient information
PROBLEM 1B
22
• For a simple, compressible substance, pressure and temperature are
known. How many additional properties are required to fix the state
of the substance?
a) 0
b) 1
c) 2
d) Insufficient information
PROBLEM 1C
23
• Which of the following most closely approaches the ideal gas
condition for a substance?
a) P >>> PCritical ; T >>> Tcritical
b) P >>> PCritical ; T <<< Tcritical
c) P <<< PCritical ; T >>> Tcritical
d) P <<< PCritical ; T >>> TCritical
PROBLEM 1D
24
• Which assumptions are required to apply W = PΔV? For a process?
Circle all that apply.
a) Ideal Gas
b) Incompressible
c) Constant Pressure
d) Quasi-Equilibrium
e) Neglect Changes in PE and KE
PROBLEM 1E
25
• Enthalpy of water at a high pressure and treated as a superheated
vapor depends only on temperature: (T/F)
• Enthalpy of water vapor at low pressure and treated as and ideal gas
depends only on temperature: (T/F)
• For a given temperature, enthalpy of a compressed liquid treated as
an incompressible is higher than enthalpy of the saturated liquid:
(T/F)
• For an incompressible substance, cp is always higher than cv: (T/F)
• For any substance and phase, cp – cv = R: (T/F)
PROBLEM 1F
26
• For any general substance undergoing a constant temperature
process in a constant mass system, is PV = Constant always true?
Justify using property diagram and/or equation.
PROBLEM 2
27
• Water with an absolute pressure of 10 bar and a quality of 0.25
(State 1) is expanded in a closed piston-cylinder device along a path
𝑃𝑣 = Constant until the absolute pressure drops to 1 bar (State 2).
– Find the quality at State 2 [%]
– Calculate the specific work during the process [kJ/kg]
– Determine the heat transfer per unit mass of water during the
process [kJ/kg]
– Show the process on a P-v diagram relative to the vapor dome
and isotherms for the two states. Label states, axes, and direction
of the process
PROBLEM 2
28
• Given
• Find
• Assumptions
• Basic Equations
PROBLEM 2
29
• Solution:
PROBLEM 2
30
PROBLEM 2
31
PROBLEM 3
32
• Two rigid tanks are connected by a pipe and a valve. The left tank with a volume of 0.5 m3 initially contains air at an absolute pressure of 2 bar and an absolute temperature of 400 K. The right tank has an initial volume of 0.25 m3 and initially contains air at an absolute pressure of 3 bar and an absolute temperature of 350 K. The valve in the pipe connecting the two tanks is opened and the air is allowed to mix until the final temperature and pressure are the same in each tank. Heat transfer of 90 kJ occurs from the air to the surroundings during the process. Mair = 28.97 kg/kmol, don’t interpolate
• Given:
• Find:
– T2 [K]
– P2 [bar]
PROBLEM 3
33
• Assumptions:
• Basic Equations:
• Solution:
PROBLEM 3
34
PROBLEM 3
35
PROBLEM 3
36
PROBLEM 3
37
38
39
40
VL = 0.5 m3
PL = 2 bar
TL = 400 K
VR = 0.25 m3
PR = 3 bar
TR = 350 K