Abstract
With recent findings of substantial amounts of B in rock-forming minerals, it has become evident a need exists for microprobe techniques allowing quantitative B determinations in minerals. A microprobe method based on the nuclear reaction 11B(p,α)2α has the potential to become a powerful tool for analyses of minerals with B contents spanning a wide concentration range. In this paper, we present nuclear microprobe analyses of B in a set of silicate minerals containing stoichiometric concentrations of B in the range 1.9-8.8 wt%. Our results strongly indicate that nuclear reaction analyses of silicates utilizing the 11B(p,α)2α nuclear reaction are virtually matrix-insensitive, and saturation effects are negligible within the studied range of B concentrations. This finding suggests that it is adequate to use a single B standard for calibration purposes for analyses covering wide ranges of B concentrations in silicates. In addition, we demonstrate how B-concentration maps of high contrast and resolution may be produced by scanning the proton beam over the samples.
© 2015 by Walter de Gruyter Berlin/Boston
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Articles in the same Issue
- Structural systematics of hydrous ringwoodite and water in earth’s interior
- Compressibility of phase Egg AlSiO3OH: Equation of state and role of water at high pressure
- Synchrotron infrared spectroscopy of OH-chondrodite and OH-clinohumite at high pressure
- Structural deformation mechanisms of zeolites under pressure
- Variation of hydrogen bonded O···O distances in goethite at high pressure
- Pressure-controlled polytypism in hydrous layered materials
- OH– in synthetic and natural coesite
- Pressure-induced phase transformation of kalicinite (KHCO3) at 2.8 GPa and local structural changes around hydrogen atoms
- Potential docking sites and positions of hydrogen in high-pressure silicates
- Contrasting bonding behavior of two hydroxyl-bearing metamorphic minerals under pressure: Clinozoisite and topaz
- Experimental investigation of crystallization kinetics in a haplogranite system
- Assessment of cation substitutions along the gallium and fluorine analogue of the tremolite-glaucophane join
- Experimental hydrothermal alteration of partially metamict zircon
- On the origin of size-dependent and size-independent crystal growth: Influence of advection and diffusion
- Ordering in spinels—A Monte Carlo study
- Single-crystal in situ high-temperature structural investigation of the I1̅ –I2/c phase transition in Ca0.2Sr0.8Al2Si2O8 feldspar
- New clinopyroxene-liquid thermobarometers for mafic, evolved, and volatile-bearing lava compositions, with applications to lavas from Tibet and the Snake River Plain, Idaho
- Fe and Ni impurities in synthetic diamond
- Phase transformations and reaction kinetics during the temperature-induced oxidation of natural olivine
- Thermal infrared spectroscopy and modeling of experimentally shocked plagioclase feldspars
- Oxygen isotopic composition of nano-scale uraninite at the Oklo-Okélobondo natural fission reactors, Gabon
- Clinopyroxenite from the Sulu ultrahigh-pressure terrane, eastern China: Origin and evolution of garnet exsolution in clinopyroxene
- Letters. An assessment of nuclear microprobe analyses of B in silicate minerals
- Incommensurate phase in the kosmochlor-diopside join: A new polymorph of clinopyroxene
- Elastic properties of hydrous ringwoodite
- Thermochemistry of guest-free melanophlogite
- A simple model for the pressure preservation index of inclusions in diamond