Literature DB >> 26032492

Bioaccessibility of micron-sized powder particles of molybdenum metal, iron metal, molybdenum oxides and ferromolybdenum--Importance of surface oxides.

Alexander Mörsdorf1, Inger Odnevall Wallinder1, Yolanda Hedberg2.   

Abstract

The European chemical framework REACH requires that hazards and risks posed by chemicals, including alloys and metals, that are manufactured, imported or used in different products (substances or articles) are identified and proven safe for humans and the environment. Metals and alloys need hence to be investigated on their extent of released metals (bioaccessibility) in biologically relevant environments. Read-across from available studies may be used for similar materials. This study investigates the release of molybdenum and iron from powder particles of molybdenum metal (Mo), a ferromolybdenum alloy (FeMo), an iron metal powder (Fe), MoO2, and MoO3 in different synthetic body fluids of pH ranging from 1.5 to 7.4 and of different composition. Spectroscopic tools and cyclic voltammetry have been employed to characterize surface oxides, microscopy, light scattering and nitrogen absorption for particle characterization, and atomic absorption spectroscopy to quantify released amounts of metals. The release of molybdenum from the Mo powder generally increased with pH and was influenced by the fluid composition. The mixed iron and molybdenum surface oxide of the FeMo powder acted as a barrier both at acidic and weakly alkaline conditions. These findings underline the importance of the surface oxide characteristics for the bioaccessibility of metal alloys.
Copyright © 2015 The Authors. Published by Elsevier Inc. All rights reserved.

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Keywords:  Alloy; Bioaccessibility; Ferromolybdenum; Molybdenum; Surface oxide

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Year:  2015        PMID: 26032492     DOI: 10.1016/j.yrtph.2015.05.027

Source DB:  PubMed          Journal:  Regul Toxicol Pharmacol        ISSN: 0273-2300            Impact factor:   3.271


  1 in total

1.  Multi-walled carbon nanotube induces nitrative DNA damage in human lung epithelial cells via HMGB1-RAGE interaction and Toll-like receptor 9 activation.

Authors:  Yusuke Hiraku; Feiye Guo; Ning Ma; Tatsuhiko Yamada; Shumin Wang; Shosuke Kawanishi; Mariko Murata
Journal:  Part Fibre Toxicol       Date:  2016-03-29       Impact factor: 9.400

  1 in total

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