Thanks Alna, for your answer! Yes, I'm sorry for the mistake, I just didn't notice it, it's actually :h=-T(dv/dT) at constant p.
Here's my answer for this question:
H=U+pv(H is the enthalpy)
H=Q+W+pv(U=Q+W)
dH=dQ+dW+d(pv)
knowing that dQ=CvdT+hdp
dH=CvdT+hdp−pdv+pdv+vdp
dH=CvdT+hdp+vdp
dH=CvdT+(h+v)dp
H is a state function, that means it's a total differential:
(∂Cv∂p)T=(∂(h+v)∂T)p
(∂Cv∂p)T=(∂h∂T)p+(∂v∂T)p(1)
On the other hand we have:
dQ=CvdT+hdp∗(1T)
dS=CvTdT+hTdp
S is a state function, that means it's a total differential:
(∂(Cv/T)∂p)T=(∂(h/T)∂T)p
1T(∂Cv∂p)T=T(∂h∂T)p−hT²T²
(∂Cv∂p)T=(∂h∂T)p−hT(2)
(1)=(2)
(∂h∂T)p+(∂v∂T)p=(∂h∂T)p−hT
(∂v∂T)p=−hT
h=−T(∂v∂T)p
.