Experimental and Theoretical Evidence for Surface-Induced Carbon and Nitrogen Fractionation during Diamond Crystallization at High Temperatures and High Pressures

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...

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Main Authors: Vadim N. Reutsky, Piotr M. Kowalski, Yury N. Palyanov, EIMF, Michael Wiedenbeck
Format: Article
Language:English
Published: MDPI AG 2017-06-01
Series:Crystals
Subjects:
Online Access:http://www.mdpi.com/2073-4352/7/7/190
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author Vadim N. Reutsky
Piotr M. Kowalski
Yury N. Palyanov
EIMF
Michael Wiedenbeck
author_facet Vadim N. Reutsky
Piotr M. Kowalski
Yury N. Palyanov
EIMF
Michael Wiedenbeck
author_sort Vadim N. Reutsky
collection DOAJ
description 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.
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spelling doaj.art-af79525b22ad4da3ab1f463992541c9a2022-12-22T04:27:26ZengMDPI AGCrystals2073-43522017-06-017719010.3390/cryst7070190cryst7070190Experimental and Theoretical Evidence for Surface-Induced Carbon and Nitrogen Fractionation during Diamond Crystallization at High Temperatures and High PressuresVadim N. Reutsky0Piotr M. Kowalski1Yury N. Palyanov2EIMF3Michael Wiedenbeck4Sobolev Institute of Geology and Mineralogy SB RAS, Novosibirsk 630090, RussiaInstitute of Energy and Climate Research (IEK-6), Forschungszentrum Juelich, 52425 Juelich, GermanySobolev Institute of Geology and Mineralogy SB RAS, Novosibirsk 630090, RussiaEdinburgh Ion Microprobe Facility, Grant Institute of Earth Sciences, School of GeoSciences, University of Edinburgh, Edinburgh EH9 3JW, UKDeutsches GeoForschungZentrum, 14473 Potsdam, GermanyIsotopic 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.http://www.mdpi.com/2073-4352/7/7/190mixed-habit diamond crystallizationcarbon isotopesnitrogen impurityfractionationexperimenthigh pressurehigh temperaturecrystal chemistrysurface structureSIMS
spellingShingle Vadim N. Reutsky
Piotr M. Kowalski
Yury N. Palyanov
EIMF
Michael Wiedenbeck
Experimental and Theoretical Evidence for Surface-Induced Carbon and Nitrogen Fractionation during Diamond Crystallization at High Temperatures and High Pressures
Crystals
mixed-habit diamond crystallization
carbon isotopes
nitrogen impurity
fractionation
experiment
high pressure
high temperature
crystal chemistry
surface structure
SIMS
title Experimental and Theoretical Evidence for Surface-Induced Carbon and Nitrogen Fractionation during Diamond Crystallization at High Temperatures and High Pressures
title_full Experimental and Theoretical Evidence for Surface-Induced Carbon and Nitrogen Fractionation during Diamond Crystallization at High Temperatures and High Pressures
title_fullStr Experimental and Theoretical Evidence for Surface-Induced Carbon and Nitrogen Fractionation during Diamond Crystallization at High Temperatures and High Pressures
title_full_unstemmed Experimental and Theoretical Evidence for Surface-Induced Carbon and Nitrogen Fractionation during Diamond Crystallization at High Temperatures and High Pressures
title_short Experimental and Theoretical Evidence for Surface-Induced Carbon and Nitrogen Fractionation during Diamond Crystallization at High Temperatures and High Pressures
title_sort experimental and theoretical evidence for surface induced carbon and nitrogen fractionation during diamond crystallization at high temperatures and high pressures
topic mixed-habit diamond crystallization
carbon isotopes
nitrogen impurity
fractionation
experiment
high pressure
high temperature
crystal chemistry
surface structure
SIMS
url http://www.mdpi.com/2073-4352/7/7/190
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