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graph theory
Second part: multiport field and
junction structures, and
thermodynamics
Multiport fields
We will look at multiport generalizations of C, I and R elements.
C-fields
f2
e1
f1
e2
en
fn
qn
= f1
= f2
..
.
= fn
State variables q1 , q2 , . . . , qn
q1
q2
e1
e2
en
= 1 (q1 , . . . , qn )
= 2 (q1 , . . . , qn )
..
.
= n (q1 , . . . , qn )
Energy is computed as
H(t) = H(t0 ) +
Z tX
n
ek ( )fk ( ) d
t0 k=1
e(
q ) d
q
i, j = 1, . . . , n
e = d
Linear case:
compliance form
q = Ce
stiness form
e = kq
all dierential
all integral
all-integral is possible
2 0 2
e 2 f2
all-dierential is not
k = 0 1 1 det k = 0
e1
e3
2 1 3
C
f1
f3
furthermore . . .
1
2
q1
e1
0 1
q2 = 0 1 1 e2
q3
e3
1 1 0
e 2 f2
e1
f1
e3
f3
is possible
C3
P1
C1
C2
P2
C : C1
C : C3
C : C2
C3
P1
C1
C2
P2
P1
5
6
e1 = e6 = e3
f6 = f 5 = f7
e4 = e7 = e2
f3 = f1 + f6
e5 = e6 e7
f4 = f7 + f2
q3 = f3
e3 =
1
C1 q3
q5 = C3 e5
f5 = q5
q4 = f4
e4 =
q5 = C3
q4
q3
+
C1
C2
f1 = i 1
1
C2 q4
q5 = C3 e5 = C3 (e6 e7 ) = C3 (e3 + e4 ) = C3
f2 = i 2
q4
q3
+
C1
C2
P2
q4
q3
q3 = f3 = f1 + f6 = i1 + f5 = i1 + q5 = i1 C3
+
C1
C2
q4
q3
q4 = f4 = f2 + f7 = i2 + f5 = i2 + q5 = i2 C3
+
C1
C2
C3
C3
1 + C1
i1
q3
C2
=
C3
C3
q4
i2
1
+
C1
C2
q3
q4
1
C1 C 2 + C 2 C3 + C 1 C 3
C 1 C2 + C1 C 3
C2 C3
C1 C3
C1 C 2 + C2 C3
i1
i2
e1
e2
1
C 1 C2 + C2 C 3 + C 1 C3
C2 + C3
C3
C3
C1 + C3
q1
q2
e1
e2
1
C 1 C2 + C2 C 3 + C 1 C3
C2 + C3
C3
C3
C1 + C3
q1
q2
k
This is a 2-port C-field in stiness form.
e1
f1
e2
f2
They are just a convenient
parametrization of the R3 surface
q5 = C3 Cq31 + Cq42
The dependent state variable has been hidden away from the port interface.
I-fields
f2
e1
f1
e2
en
fn
State variables p1 , p2 , . . . , pn
p1
p2
pn
= e1
= e2
..
.
= en
f1
f2
fn
= 1 (p1 , . . . , pn )
= 2 (p1 , . . . , pn )
..
.
= n (p1 , . . . , pn )
Energy:
H(p) = H(p0 ) +
f (
p) d
p
j
i
=
,
pj
pi
i, j = 1, . . . , n
independence of
V2
V1
CM
F2
F1
V1
V2
1
m
1
m
L
4J2
L
4J
1
m
1
m
L
4J2
L
4J
p1
p2
IC-fields
fI
e1
f1
eI e1 f
1
IC
eC
p1
pI
q1
fC
qC
=
..
.
=
=
..
.
=
e1
f1
eI
f1
fI
e1
fC
eC
=
..
.
=
=
..
.
=
1 (p1 , . . . , pI , q1 , . . . , qC )
I (p1 , . . . , pI , q1 , . . . , qC )
1 (p1 , . . . , pI , q1 , . . . , qC )
I (p1 , . . . , pI , q1 , . . . , qC )
i, j = 1, . . . , I
j
i
=
,
qj
pi
j
i
=
,
qj
qi
i, j = 1, . . . , C
i = 1, . . . , I, j = 1, . . . , C
P1
GY
..
m
= f1
p5
= e6
1
e6
m
P2
C:C
q2
I :L
e1
f6
1
1
q
p
C
mC
1
1
1
q+
+ 2
p
=
mC
L m C
1
m p5
Maxwell condition
R-fields
f2
e1
f1
Onsager forms
e2
en
fn
resistance form
e = (f )
conductance form
f = 1 (e)
P1
e1
f1
R : R3
GY : m
e2
f2
e1
e2
R : R5
P2
R : R4
R3 + R4
m + R4
m + R4
R4 + R5
f1
f2
Junction structures
Assemblages of 0, 1, TF and GY elements which switch energy around.
Limiting cases of R-fields (without sources)which do not dissipate.
Unless modulated TF or GY elements are present, eort/flow
constitutive relations in a junction structure are always linear.
With an all-input power sign convention, the matrix
relating inputs to outputs must be antisymmetric.
Causality patterns are more restricted, though.
Junction structures without gyrators cannot accept
conductance or resistance causality on all ports.
P1
m : TF
GY
0
f1
e2 = m
f3
m
r
:r
P2
P3
m
r
m
e1
0
m f2
m
0
e3
P3
P4
:m
TF
P2
TF
..
m2
e1
e2
1
m1
1
m2
e3
e4
M
..
TF
f3
f4
1 m1
1 m2
f1
f2
Thermodynamics from
the bond graph point of view
Pure substance with no motion, constant mass and
no electromagnetic or surface-tension forces:
internal energy
per unit mass
u = u(s, v)
entropy
per unit mass
Gibbs equation:
volume
per unit mass
du = T ds p dv
absolute temperature
pressure
u
T =
s
du = T ds p dv
u
p =
v
T = T (s, v)
p = p(s, v)
(p)
T
=
v
s
constitutive
equations
entalphy h
Gibbs equation
h = u + pv
dh = du + p dv + v dp = T ds + v dp
h = h(s, p)
constitutive equations
T
v
=
=
T (s, p)
v(s, p)
mixed causality
T
v
Maxwell condition
h
s
h
p
=
=
T
s
v
T
=
p
s
f = u Ts
df = du T ds s dT = s dT p dv
f = f (T, v)
constitutive equations
s = s(T, v)
p = p(T, v)
mixed causality
p =
Maxwell condition
f
T
f
v
T
s
s
p
=
T
v
d = du + p dv + v dp T ds s dT
= s dT + v dp
= (T, p)
Gibbs equation
constitutive equations
s =
v =
s(T, p)
v(T, p)
All-dierential causality
s =
v
Maxwell condition
(s)
v
=
T
p
T
s
s
p
v
T
s=
s dt
h = h(s, p)
2h
2h
s
v =
p +
2
p
sp
h
s
h
p
u
T
cp = cv + R
cv =
u
T
cv constant
h = u + RT
u = cv (T T0 )
h is also function
of T alone
h
cp =
T
reference
temperature
h = cp (T T0 ) + RT0
cp constant
due to cp = cv + R
dv
dv
du
dT
du = T ds p dv
+p
+R
ds =
= cv
T
T
T
v
cR
v
T
v
s
v
c
s = cv log
+ R log
T = T0 e v
T0
v0
v0
integration of
the 1-form
dh = T ds + v dp
ds =
dp
dp
dh
dT
v
v
= cp
T
T
T
T
v
1
v cp
dv
dv
dp
(p dv + v dp) dp = cp
= cp
+
1 dp = cp
+ cv
RT
T
v
T R
v
p
v
p
s = cp log
+ cv log
v0
p0
integration of
the 1-form
p = p0 e
s
cv
T = T0 e
s
cv
v
v0
ccp
v
v0
cR
p = p0 e
s
cv
v
v0
ccp
R, cv
Chemical engineering:
transport phenomena
quantities of substances vary with time
Requires an extension of the basic
thermodynamic bond graph framework
fuel cells