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Experimental and theoretical evidence for surface-induced carbon and nitrogen fractionation during diamond crystallization at high temperatures and high pressures. / Reutsky, Vadim N.; Kowalski, Piotr M.; Palyanov, Yury N. et al.

In: Crystals, Vol. 7, No. 7, 190, 01.07.2017.

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@article{0964d3951dd2414c8b5420940420e542,
title = "Experimental and theoretical evidence for surface-induced carbon and nitrogen fractionation during diamond crystallization at high temperatures and high pressures",
abstract = "Isotopic and trace element variations within single diamond crystals are widely known from both natural stones and synthetic crystals. A number of processes can produce variations in carbon isotope composition and nitrogen abundance in the course of diamond crystallization. Here, we present evidence of carbon and nitrogen fractionation related to the growing surfaces of a diamond. We document that difference in the carbon isotope composition between cubic and octahedral growth sectors is solvent-dependent and varies from 0.7‰ in a carbonate system to 0.4‰ in a metal-carbon system. Ab initio calculations suggest up to 4‰ instantaneous 13C depletion of cubic faces in comparison to octahedral faces when grown simultaneously. Cubic growth sectors always have lower nitrogen abundance in comparison to octahedral sectors within synthetic diamond crystals in both carbonate and metal-carbon systems. The stability of any particular growth faces of a diamond crystal depends upon the degree of carbon association in the solution. Octahedron is the dominant form in a high-associated solution while the cube is the dominant form in a low-associated solution. Fine-scale data from natural crystals potentially can provide information on the form of carbon, which was present in the growth media.",
keywords = "Carbon isotopes, Crystal chemistry, Experiment, Fractionation, High pressure, High temperature, Mixed-habit diamond crystallization, Nitrogen impurity, SIMS, Surface structure, HABIT, nitrogen impurity, UDACHNAYA-EAST KIMBERLITE, DEEP MANTLE, HIGH P, experiment, CRYSTAL-GROWTH, SYNTHETIC DIAMOND, mixed-habit diamond crystallization, fractionation, crystal chemistry, IMPURITY, surface structure, high pressure, high temperature, NATURAL DIAMOND, GROWTH-SECTOR DEPENDENCE, carbon isotopes, ISOTOPE FRACTIONATION",
author = "Reutsky, {Vadim N.} and Kowalski, {Piotr M.} and Palyanov, {Yury N.} and Michael Wiedenbeck",
year = "2017",
month = jul,
day = "1",
doi = "10.3390/cryst7070190",
language = "English",
volume = "7",
journal = "Crystals",
issn = "2073-4352",
publisher = "Multidisciplinary Digital Publishing Institute (MDPI)",
number = "7",

}

RIS

TY - JOUR

T1 - Experimental and theoretical evidence for surface-induced carbon and nitrogen fractionation during diamond crystallization at high temperatures and high pressures

AU - Reutsky, Vadim N.

AU - Kowalski, Piotr M.

AU - Palyanov, Yury N.

AU - Wiedenbeck, Michael

PY - 2017/7/1

Y1 - 2017/7/1

N2 - Isotopic and trace element variations within single diamond crystals are widely known from both natural stones and synthetic crystals. A number of processes can produce variations in carbon isotope composition and nitrogen abundance in the course of diamond crystallization. Here, we present evidence of carbon and nitrogen fractionation related to the growing surfaces of a diamond. We document that difference in the carbon isotope composition between cubic and octahedral growth sectors is solvent-dependent and varies from 0.7‰ in a carbonate system to 0.4‰ in a metal-carbon system. Ab initio calculations suggest up to 4‰ instantaneous 13C depletion of cubic faces in comparison to octahedral faces when grown simultaneously. Cubic growth sectors always have lower nitrogen abundance in comparison to octahedral sectors within synthetic diamond crystals in both carbonate and metal-carbon systems. The stability of any particular growth faces of a diamond crystal depends upon the degree of carbon association in the solution. Octahedron is the dominant form in a high-associated solution while the cube is the dominant form in a low-associated solution. Fine-scale data from natural crystals potentially can provide information on the form of carbon, which was present in the growth media.

AB - Isotopic and trace element variations within single diamond crystals are widely known from both natural stones and synthetic crystals. A number of processes can produce variations in carbon isotope composition and nitrogen abundance in the course of diamond crystallization. Here, we present evidence of carbon and nitrogen fractionation related to the growing surfaces of a diamond. We document that difference in the carbon isotope composition between cubic and octahedral growth sectors is solvent-dependent and varies from 0.7‰ in a carbonate system to 0.4‰ in a metal-carbon system. Ab initio calculations suggest up to 4‰ instantaneous 13C depletion of cubic faces in comparison to octahedral faces when grown simultaneously. Cubic growth sectors always have lower nitrogen abundance in comparison to octahedral sectors within synthetic diamond crystals in both carbonate and metal-carbon systems. The stability of any particular growth faces of a diamond crystal depends upon the degree of carbon association in the solution. Octahedron is the dominant form in a high-associated solution while the cube is the dominant form in a low-associated solution. Fine-scale data from natural crystals potentially can provide information on the form of carbon, which was present in the growth media.

KW - Carbon isotopes

KW - Crystal chemistry

KW - Experiment

KW - Fractionation

KW - High pressure

KW - High temperature

KW - Mixed-habit diamond crystallization

KW - Nitrogen impurity

KW - SIMS

KW - Surface structure

KW - HABIT

KW - nitrogen impurity

KW - UDACHNAYA-EAST KIMBERLITE

KW - DEEP MANTLE

KW - HIGH P

KW - experiment

KW - CRYSTAL-GROWTH

KW - SYNTHETIC DIAMOND

KW - mixed-habit diamond crystallization

KW - fractionation

KW - crystal chemistry

KW - IMPURITY

KW - surface structure

KW - high pressure

KW - high temperature

KW - NATURAL DIAMOND

KW - GROWTH-SECTOR DEPENDENCE

KW - carbon isotopes

KW - ISOTOPE FRACTIONATION

UR - http://www.scopus.com/inward/record.url?scp=85021660564&partnerID=8YFLogxK

U2 - 10.3390/cryst7070190

DO - 10.3390/cryst7070190

M3 - Article

AN - SCOPUS:85021660564

VL - 7

JO - Crystals

JF - Crystals

SN - 2073-4352

IS - 7

M1 - 190

ER -

ID: 10096327