The structure and transformation of the nanomineral schwertmannite: a synthetic analog representative of field samples

Abstract The phase transformation of schwertmannite, an iron oxyhydroxide sulfate nanomineral synthesized at room temperature and at 75 °C using H2O2 to drive the precipitation of schwertmannite from ferrous sulfate (Regenspurg et al. in Geochim Cosmochim Acta 68:1185–1197, 2004), was studied using high-resolution transmission electron microscopy. The results of this study suggest that schwertmannite synthesized using this method should not be described as a single phase with a repeating unit cell, but as a polyphasic nanomineral with crystalline areas spanning less than a few nanometers in diameter, within a characteristic ‘pin-cushion’-like amorphous matrix. The difference in synthesis temperature affected the density of the needles on the schwertmannite surface. The needles on the higher-temperature schwertmannite displayed a dendritic morphology, whereas the needles on the room-temperature schwertmannite were more closely packed. Visible lattice fringes in the schwertmannite samples are consistent with the powder X-ray diffraction (XRD) pattern taken on the bulk schwertmannite and also matched d-spacings for goethite, indicating a close structural relationship between schwertmannite and goethite. The incomplete transformation from schwertmannite to goethite over 24 h at 75 °C was tracked using XRD and TEM. TEM images suggest that the sample collected after 24 h consists of aggregates of goethite nanocrystals. Comparing the synthetic schwertmannite in this study to a study on schwertmannite produced at 85 °C, which used ferric sulfate, reveals that synthesis conditions can result in significant differences in needle crystal structure. The bulk powder XRD patterns for the schwertmannite produced using these two samples were indistinguishable from one another. Future studies using synthetic schwertmannite should account for these differences when determining schwertmannite’s structure, reactivity, and capacity to take up elements like arsenic. The schwertmannite synthesized by the Regenspurg et al. method produces a mineral that is consistent with the structure and morphology of natural schwertmannite observed in our previous study using XRD and TEM, making this an ideal synthetic method for laboratory-based mineralogical and geochemical studies that intend to be environmentally relevant.

[1]  Udo Schwertmann,et al.  A poorly crystallized oxyhydroxysulfate of iron formed by bacterial oxidation of Fe(II) in acid mine waters , 1990 .

[2]  U. Schwertmann,et al.  Iron Oxides in the Laboratory: Preparation and Characterization , 1991 .

[3]  E. Murad,et al.  Schwertmannite, a new iron oxyhydroxysulphate from Pyhäsalmi, Finland, and other localities , 1994, Mineralogical Magazine.

[4]  J. Banfield,et al.  Chemical weathering of silicates in nature; a microscopic perspective with theoretical considerations , 1995 .

[5]  S. Brantley,et al.  Chemical weathering rates of silicate minerals , 1995 .

[6]  Jerry M. Bigham,et al.  SCHWERTMANNITE AND THE CHEMICAL MODELING OF IRON IN ACID SULFATE WATERS , 1996 .

[7]  Jerry M. Bigham,et al.  Influence of pH on mineral speciation in a bioreactor simulating acid mine drainage , 1996 .

[8]  R. Barham Schwertmannite: A unique mineral, contains a replaceable ligand, transforms to jarosites, hematites, and/or basic iron sulfate , 1997 .

[9]  J. E. Dutrizac,et al.  The behaviour of zinc, cadmium, thallium, tin and selenium during ferrihydrite precipitation from sulphate media , 1998 .

[10]  J. M. Cowley,et al.  Structure of synthetic 2-line ferrihydrite by electron nanodiffraction , 2000 .

[11]  D. Nordstrom,et al.  Iron and Aluminum Hydroxysulfates from Acid Sulfate Waters , 2000 .

[12]  J. Banfield,et al.  Aggregation-based crystal growth and microstructure development in natural iron oxyhydroxide biomineralization products. , 2000, Science.

[13]  U. Schwertmann,et al.  Iron Oxides in the Laboratary , 2000 .

[14]  G. Plumlee Sulfate minerals- Crystallography, geochemistry and environmental significance , 2001 .

[15]  G. Waychunas Structure, Aggregation and Characterization of Nanoparticles , 2001 .

[16]  U. Schwertmann,et al.  Scavenging of As from acid mine drainage by schwertmannite and ferrihydrite: a comparison with synthetic analogues. , 2002, Environmental science & technology.

[17]  J. O. Claassen,et al.  Iron precipitation from zinc-rich solutions: defining the Zincor Process , 2002 .

[18]  U. Schwertmann,et al.  Iron Oxides , 2003, SSSA Book Series.

[19]  A. Brand,et al.  Formation and stability of schwertmannite in acidic mining lakes , 2004 .

[20]  Michael D. Abràmoff,et al.  Image processing with ImageJ , 2004 .

[21]  J. M. Cowley,et al.  Evidence on the structure of synthetic schwertmannite , 2004 .

[22]  A. Navrotsky Energetic clues to pathways to biomineralization: precursors, clusters, and nanoparticles. , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[23]  R. L. Penn,et al.  Reduction of crystalline iron(III) oxyhydroxides using hydroquinone: Influence of phase and particle size , 2005, Geochemical transactions.

[24]  R. Parnell,et al.  Trace metal retention through the schwertmannite to goethite transformation as observed in a field setting, Alta Mine, MT , 2005 .

[25]  A. S. Madden,et al.  A test of geochemical reactivity as a function of mineral size: Manganese oxidation promoted by hematite nanoparticles , 2005 .

[26]  P. Persson,et al.  Schwertmannite precipitated from acid mine drainage: phase transformation, sulphate release and surface properties , 2005 .

[27]  U. Schwertmann,et al.  The pH-dependent transformation of schwertmannite to goethite at 25°C , 2005, Clay Minerals.

[28]  Pratim Biswas,et al.  Nanoparticles and the Environment , 2005 .

[29]  E. Santofimia,et al.  Acid mine drainage in the Iberian Pyrite Belt (Odiel river watershed, Huelva, SW Spain): Geochemistry, mineralogy and environmental implications , 2005 .

[30]  J. Majzlan,et al.  Speciation of iron and sulfate in acid waters: aqueous clusters to mineral precipitates. , 2005, Environmental science & technology.

[31]  S. Peiffer,et al.  Arsenate and chromate incorporation in schwertmannite , 2005 .

[32]  R. L. Penn,et al.  Two-step growth of goethite from ferrihydrite. , 2006, Langmuir : the ACS journal of surfaces and colloids.

[33]  C. Ayora,et al.  The behavior of trace elements during schwertmannite precipitation and subsequent transformation into goethite and jarosite , 2006 .

[34]  Michael F. Hochella,et al.  Insights for size-dependent reactivity of hematite nanomineral surfaces through Cu2+ sorption , 2006 .

[35]  R. L. Penn,et al.  Controlled growth of alpha-FeOOH nanorods by exploiting-oriented aggregation , 2006 .

[36]  L. Lövgren,et al.  Precipitation of secondary Fe(III) minerals from acid mine drainage , 2006 .

[37]  C. Blodau,et al.  Controls on schwertmannite transformation rates and products , 2007 .

[38]  R. Bush,et al.  Catalytic action of aqueous Fe(II) and S(II) on the transformation of schwertmannite to goethite , 2007 .

[39]  M. Schoonen,et al.  The Structure of Ferrihydrite, a Nanocrystalline Material , 2007, Science.

[40]  D. Mitchell,et al.  Reductive transformation of iron and sulfur in schwertmannite-rich accumulations associated with acidified coastal lowlands , 2007 .

[41]  Michael F. Hochella,et al.  The non-oxidative dissolution of galena nanocrystals: Insights into mineral dissolution rates as a function of grain size, shape, and aggregation state , 2008 .

[42]  D. Mitchell,et al.  Schwertmannite transformation to goethite via the Fe(II) pathway: reaction rates and implications for iron-sulfide formation , 2008 .

[43]  D. Sparks,et al.  Nanominerals, Mineral Nanoparticles, and Earth Systems , 2008, Science.

[44]  L. Benning,et al.  The kinetics and mechanisms of schwertmannite transformation to goethite and hematite under alkaline conditions , 2008 .

[45]  Mitsuhiro Murayama,et al.  Influence of size and aggregation on the reactivity of an environmentally and industrially relevant nanomaterial (PbS). , 2009, Environmental science & technology.

[46]  F. Jones,et al.  An electron microscopy study of the crystal growth of schwertmannite needles through oriented aggregation of goethite nanocrystals , 2009 .

[47]  C. Ayora,et al.  Natural attenuation of arsenic in the Tinto Santa Rosa acid stream (Iberian Pyritic Belt, SW Spain): The role of iron precipitates , 2010 .

[48]  R. Bush,et al.  Arsenic effects and behavior in association with the Fe(II)-catalyzed transformation of schwertmannite. , 2010, Environmental science & technology.

[49]  C. Ayora,et al.  The structure of schwertmannite, a nanocrystalline iron oxyhydroxysulfate , 2010 .

[50]  M. Murayama,et al.  Influence of size, morphology, surface structure, and aggregation state on reductive dissolution of hematite nanoparticles with ascorbic acid , 2012 .

[51]  J. Rimstidt,et al.  The enigmatic iron oxyhydroxysulfate nanomineral schwertmannite: Morphology, structure, and composition , 2012 .

[52]  E. Burton,et al.  Impact of silica on the reductive transformation of schwertmannite and the mobilization of arsenic , 2012 .

[53]  C H Wu,et al.  A software tool for automatic analysis of selected area diffraction patterns within Digital Micrograph™. , 2012, Ultramicroscopy.

[54]  Jillian F Banfield,et al.  Direction-Specific Interactions Control Crystal Growth by Oriented Attachment , 2012, Science.

[55]  G. Brown,et al.  Structure and reactivity of As(III)- and As(V)-rich schwertmannites and amorphous ferric arsenate sulfate from the Carnoulès acid mine drainage, France: Comparison with biotic and abiotic model compounds and implications for As remediation , 2013 .