The distribution of rare earth elements between monzogranitic melt and theaqueous volatile phase in experimental investigations at 800 degrees C and200 MPa
Mj. Reed et al., The distribution of rare earth elements between monzogranitic melt and theaqueous volatile phase in experimental investigations at 800 degrees C and200 MPa, CONTR MIN P, 140(2), 2000, pp. 251-262
The partitioning of the rare earth elements between a peraluminous monzogra
nitic melt and a chloride-bearing, sulfur- and carbon dioxide-free, aqueous
volatile phase was examined experimentally as a function of chloride and m
ajor element concentrations at 800 degreesC and 200 MPa. The light rare ear
th elements (e.g. La, Ce) partition into the aqueous volatile phase to a gr
eater extent than the heavy rare earth elements (e.g. Yb, Lu). Distribution
of the rare earth elements and the major elements H, Na, K, Ca, and Al bet
ween the melt phase (mp) and aqueous volatile phase tag) is a function of t
he chlorine concentration in the system, and our data are consistent with t
he rare earth and major elements occurring as chloride complexes in the aqu
eous Volatile phase. Apparent equilibrium constants for experiments, at 800
degreesC and 200 MPa, K-REE1Na('aq/mp), expressed as the ratio as the rati
o of the concentration of a given rare earth element in the aqueous volatil
e phase to the concentration of the same element in the melt phase, divided
by the cubed ratio of sodium in the aqueous volatile phase to the concentr
ation of sodium in the melt phase, decrease systematically with increasing
atomic number from K-La,Na('aq/mp) = 0.41(+/-0.03) to K-Lu,Na('aq/mp) = 0.1
1(+/-0.01), except for Eu. These experimentally derived apparent equilibriu
m constants for the rare earth elements can be used in a numerical simulati
on of magmatic volatile exsolution. The simulation gave results consistent
with the elemental distribution in the potassic alteration zone of a deep p
orphyry copper deposit, but higher concentrations of heavy rare earth eleme
nts are released into the magmatic aqueous solution than are captured in th
e secondary mineralization.