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. 2000 Oct 17;97(22):11875–11879. doi: 10.1073/pnas.220408697

Table 1.

Thermoelastic properties of diamond and coesite

Parameter Designation Units Diamond Coesite
Bulk modulus Ko = −V(dP/dV)T GPa 442 99.8
Its pressure derivative Ko = (dKo/dP)T 4 6.3
Its temperature derivative (dKo/dT)P GPa/K −0.0188 −0.020§
Shear modulus μd GPa 538
Thermal expansivity α = 1/V(dV/dT)P = a + bT + cT2 + dT3 1/K
Coefficients in equation for α a*106 6.828 5.43
b*106 0.042 0.005
c*1010 −0.309 0
d*1015 8.88
Raman shift vs. pressure dν/dP cm−1/GPa 2.9 (±0.1)‡‡

The ΔV/V term at constant temperature, for both diamond and coesite, can be found from a simple Murnaghan equation of state, P = Ko/Ko[(Vo/V)Ko + 1], where K(P) = Ko + KoP and K(T) = Ko + (dK/dT)dT. The temperature dependence of the diamond bulk modulus is below the error limits and can be effectively neglected. The pressure dependence of thermal expansivity may also be neglected, especially taking into account the very small difference in thermal expansion between coesite and diamond. 

Ref. 51

Refs. 32 and 33

§

Ref. 53

Ref. 54

Ref. 52

‡‡

Ref. 27