Silicate Melting and Volatile Loss During Differentiation in Planetesimals

Planetesimals ◽  
2017 ◽  
pp. 115-135 ◽  
Author(s):  
Roger R. Fu ◽  
Edward D. Young ◽  
Richard C. Greenwood ◽  
Linda T. Elkins-Tanton
Keyword(s):  
2013 ◽  
Vol 779-780 ◽  
pp. 12-16
Author(s):  
Ping Yang ◽  
Yong Cheng

Established the analytical method by using ultrasonic vibration - suspension of solid sampling graphite furnace atomic absorption spectrometry (GF-AAS) to test trace mercury in the titanium dioxide, by choosing a suitable concentration of agar solution as dispersing agent, and taking the ultrasonic oscillation technique to prepare uniform and stable titanium dioxide suspended solid solution, and finally using the solid injection sampling GF-AAS method to test trace elements of mercury.. Through the application of solid injection technique, the problem that the titanium dioxide is extremely difficult to digest and mercury volatile loss are solved and the matrix effect of the high titanium is eliminated by standard addition method as well. The paper has tested the conditions of preparation of solid suspension such as agar dispersing agent concentration, dosage, and ultrasonic vibration parameters. and titanium dioxide solid suspensions obtained by the method have the characters of uniformity, stability, mobility features, and preserve a long time. Graphite furnace testing procedures are also optimized: drying temperature 85 °C, time 30 s, by lowering the drying temperature and measures to extend the time to solve the contradiction of water evaporation and mercury volatilization; cancel the ashing step directly into the atomization stage in order to avoid mercury loss after drying. Finally, set atomic temperature 1 000 °C, for 5 s and close the purged argon flow of the internal graphite tube to ensure mercury exists as different forms such as free, particle adsorption or parcels can be effective tested. The detection limit is from 0.000 to 005% and recovery rate is from 93% to 109%, RSD <3.1%. The results of the test is correspond with that of Microwave Digestion and Inductively Coupled Plasma Mass Spectrometry method. The methods can meet the requirement of testing toxic trace elements mercury in high-grade titanium dioxide which used in medical, food, ceramics and other field.


2018 ◽  
Vol 115 (43) ◽  
pp. 10920-10925 ◽  
Author(s):  
Paolo A. Sossi ◽  
Frédéric Moynier ◽  
Kirsten van Zuilen

Terrestrial and lunar rocks share chemical and isotopic similarities in refractory elements, suggestive of a common precursor. By contrast, the marked depletion of volatile elements in lunar rocks together with their enrichment in heavy isotopes compared with Earth’s mantle suggests that the Moon underwent evaporative loss of volatiles. However, whether equilibrium prevailed during evaporation and, if so, at what conditions (temperature, pressure, and oxygen fugacity) remain unconstrained. Chromium may shed light on this question, as it has several thermodynamically stable, oxidized gas species that can distinguish between kinetic and equilibrium regimes. Here, we present high-precision Cr isotope measurements in terrestrial and lunar rocks that reveal an enrichment in the lighter isotopes of Cr in the Moon compared with Earth’s mantle by 100 ± 40 ppm per atomic mass unit. This observation is consistent with Cr partitioning into an oxygen-rich vapor phase in equilibrium with the proto-Moon, thereby stabilizing the CrO2 species that is isotopically heavy compared with CrO in a lunar melt. Temperatures of 1,600–1,800 K and oxygen fugacities near the fayalite–magnetite–quartz buffer are required to explain the elemental and isotopic difference of Cr between Earth’s mantle and the Moon. These temperatures are far lower than modeled in the aftermath of a giant impact, implying that volatile loss did not occur contemporaneously with impact but following cooling and accretion of the Moon.


Author(s):  
Corbin L. Kling ◽  
Paul K. Byrne ◽  
Rachel M. Atkins ◽  
Karl W. Wegmann

2019 ◽  
Vol 528 ◽  
pp. 119279 ◽  
Author(s):  
John B. Creech ◽  
Frédéric Moynier ◽  
Christian Koeberl

Minerals ◽  
2020 ◽  
Vol 10 (11) ◽  
pp. 995 ◽  
Author(s):  
Hans G.M. Eggenkamp ◽  
Michael A.W. Marks ◽  
Petya Atanasova ◽  
Thomas Wenzel ◽  
Gregor Markl

We determined the halogen (F, Cl, Br, and I) and sulfur (S) concentrations in Cl-rich rock-forming minerals from five peralkaline complexes. We investigated sodalite (N = 42), eudialyte-group minerals (N = 84), and tugtupite (N = 8) from representative rock samples derived from Ilímaussaq (South Greenland), Norra Kärr (Sweden), Tamazeght (Morocco), Lovozero, and Khibina (Russian Federation). Taken together, sodalite and eudialyte-group minerals dominate the Cl and Br budget of the investigated rocks. For F, however, several other phases (e.g., amphibole, fluorite, villiaumite, and minerals of the rinkite group and the apatite supergroup) are additional sinks, and parts of the S may be scavenged in generally rare sulfides. The investigated minerals contain Cl at the wt.% level, F and S concentrations are in the hundreds to thousands of µg/g-range, Br is less common (0.2–200 µg/g) and I is rare (mostly well below 1 µg/g). Normalized to Cl, sodalite prefers Br relative to eudialyte-group minerals, while F is always enriched in the latter. Our data show that both F and S may represent important components in eudialyte-group minerals, sometimes at similar levels as Cl, which normally dominates. Sulfur reveals redox-dependent behavior: Under reduced crystallization conditions, S is more compatible in eudialyte-group minerals (EGM) than in sodalite, which flips to the opposite under water-rich and presumably more oxidized conditions. We investigate the applicability of F/Cl, Br/Cl, and S/Cl ratios in these minerals in peralkaline systems to better understand the interplay of magmatic differentiation, fluid loss and hydrothermal overprint. Similar to apatite in metaluminous systems, fractionation of sodalite, and eudialyte-group minerals in peralkaline magmas leads to decreasing Br/Cl ratios. The data presented in this study bear implications for the mineral chemistry and compositional variation of sodalite and especially EGM in general. Volatile components in EGM that are not normally considered, such as F and S, can reach concentrations of thousands of µg/g. Especially in the case of F, with its low atomic weight, the results obtained in this study indicate that it is very significant for formulae calculations, neutral charge-balance, and similar aspects at such concentration levels. This study demonstrates that halogen contents and ratios are sensitive monitors for a variety of processes in magmatic-hydrothermal systems, including magmatic fractionation, volatile loss, and fluid–rock interaction.


2014 ◽  
Vol 111 (48) ◽  
pp. 17029-17032 ◽  
Author(s):  
Emily A. Pringle ◽  
Frédéric Moynier ◽  
Paul S. Savage ◽  
James Badro ◽  
Jean-Alix Barrat

1986 ◽  
Vol 80 (3-4) ◽  
pp. 201-207 ◽  
Author(s):  
James A. Tyburczy ◽  
Benjamin Frisch ◽  
Thomas J. Ahrens

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