TY - JOUR
T1 - Improved oxygen-buffering techniques for C-O-H fluid-saturated experiments at high pressure
AU - Taylor, W. R.
AU - Foley, S. F.
PY - 1989
Y1 - 1989
N2 - A new oxygen-buffering technique has been developed for
experiments in high-pressure, solid media apparatus where saturation with a
reduced C-O-H fluid is required. The buffer (abbreviated “WCWO”) consists of a
mixture of WC, WO2 and graphite. Stearic acid (C18H36O2)
is mixed with the buffer components to provide the C-O-H fluid source. The
silicate sample is enclosed and separated from the buffer by an inner graphite
capsule thereby eliminating iron loss problems. Analysis of quenched fluids by
capsule piercing/mass spectrometry demonstrates that WCWO controls oxygen
fugacity (ƒO2) at ∼1 log unit above the iron-wustite
(IW) buffer with a reproducibility better than 0.2 logƒO2 units.
Fluid compositions buffered by WCWO can be maintained in sealed noble metal
capsules for run times exceeding 50 hours. Fluids are CH4-H2O
dominated with a wider compositional range (CH4/(CH4 +
H2O) ∼0.8 to 0.1 depending on temperature) than is accessible
with the more reduced iron-wustite-graphite (IWG) buffer. In liquidus
experiments on olivine lamproite, we found the IWG buffer, in contrast to WCWO,
to be unreliable in controlling fluid compositions. IWG did, however, perform
satisfactorily in the absence of a silicate sample. We show that the IWG
technique can be modified so that fluids of H2O ≫
CH4 > CO2 character can be reliably
reproduced (termed the “CWI” technique). The WCWO buffer has been employed in
melting studies on the system peridotite-C-O-H (Taylor and Green, 1988b)
and should have wide application in experiments above 1000°C where control of
ƒO2 and water activity (aH2O) is required.
The CWI technique is based on fluid monitoring and may be used in experiments
where high water activity but low ƒO2 (∼IW+1.5 log
units) is desired.
AB - A new oxygen-buffering technique has been developed for
experiments in high-pressure, solid media apparatus where saturation with a
reduced C-O-H fluid is required. The buffer (abbreviated “WCWO”) consists of a
mixture of WC, WO2 and graphite. Stearic acid (C18H36O2)
is mixed with the buffer components to provide the C-O-H fluid source. The
silicate sample is enclosed and separated from the buffer by an inner graphite
capsule thereby eliminating iron loss problems. Analysis of quenched fluids by
capsule piercing/mass spectrometry demonstrates that WCWO controls oxygen
fugacity (ƒO2) at ∼1 log unit above the iron-wustite
(IW) buffer with a reproducibility better than 0.2 logƒO2 units.
Fluid compositions buffered by WCWO can be maintained in sealed noble metal
capsules for run times exceeding 50 hours. Fluids are CH4-H2O
dominated with a wider compositional range (CH4/(CH4 +
H2O) ∼0.8 to 0.1 depending on temperature) than is accessible
with the more reduced iron-wustite-graphite (IWG) buffer. In liquidus
experiments on olivine lamproite, we found the IWG buffer, in contrast to WCWO,
to be unreliable in controlling fluid compositions. IWG did, however, perform
satisfactorily in the absence of a silicate sample. We show that the IWG
technique can be modified so that fluids of H2O ≫
CH4 > CO2 character can be reliably
reproduced (termed the “CWI” technique). The WCWO buffer has been employed in
melting studies on the system peridotite-C-O-H (Taylor and Green, 1988b)
and should have wide application in experiments above 1000°C where control of
ƒO2 and water activity (aH2O) is required.
The CWI technique is based on fluid monitoring and may be used in experiments
where high water activity but low ƒO2 (∼IW+1.5 log
units) is desired.
UR - http://www.scopus.com/inward/record.url?scp=0024525395&partnerID=8YFLogxK
U2 - 10.1029/JB094iB04p04146
DO - 10.1029/JB094iB04p04146
M3 - Article
AN - SCOPUS:0024525395
VL - 94
SP - 4146
EP - 4158
JO - Journal of Geophysical Research
JF - Journal of Geophysical Research
SN - 0148-0227
IS - B4
ER -