TY - JOUR
T1 - Influence of size, morphology, surface structure, and aggregation state on reductive dissolution of hematite nanoparticles with ascorbic acid
AU - Echigo, Takuya
AU - Aruguete, Deborah M.
AU - Murayama, Mitsuhiro
AU - Hochella, Michael F.
N1 - Funding Information:
T.E. acknowledges supports from the Japan Society for the Promotion of Science, Research Fellowships for Young Scientists (PD20-1531), Japan Excellent Young Researcher Overseas Visit Program , Grant-in-Aid for Research Activity Start-up (# 23840049 ) and Fukada Geological Institute (2011#7). Grants from the U.S. Department of Energy (DE-FG02-06ER15786) and the Institute for Critical Technology and Applied Science at Virginia Tech provided financial support for this study, as well as a grant from the National Science Foundation (NSF) and the Environmental Protection Agency (EPA) under NSF Cooperative Agreement EF-0830093, entitled Center for the Environmental Implications of Nanotechnology (CEINT). D.M.A. acknowledges support from NSF grant DEB-0610373 (Postdoctoral Fellowship) during part of this work. This manuscript was completed during her current service at NSF. Any opinions, findings, and conclusions or recommendations expressed in this material are those of the authors and do not necessarily reflect the views of the National Science Foundation. Important assistance from Dr. Madeline Schreiber (anaerobic chamber work), Dr. Niven Monsegue (TEM at the Nanoscale Characterization and Fabrication Laboratory), Dr. Ted Oyama and Phuong Bui (BET surface area analysis), and Carol Johnson (DLS measurements) are gratefully acknowledged. We thank Prof. Donald Rimstidt, Dr. Bojeong Kim, Dr. Dongbo Wang, Dr. Rebecca French, Dr. Harish Veeramani, and James Dale for helpful discussions. The authors are indebted to the Associate Editor, Dr. Chris Kim, and three anonymous reviewers for valuable comments for improving the paper.
PY - 2012/8/1
Y1 - 2012/8/1
N2 - Nanoscale iron (oxyhydr)oxide minerals are omnipresent in natural environments and past studies have found that their size, morphology, surface structure, and aggregation state influence chemical reactivity. In this study, we have investigated the influence of these factors on the reductive dissolution of hematite with ascorbic acid using two types of nanoparticles with average diameters of 6.8±0.8nm and 30.5±3.5nm, referred to as Hem-7 and Hem-30, respectively, in this paper. Hematite nanoparticles were synthesized by forced hydrolysis of ferric nitrate and characterized with powder XRD, TEM, and BET surface area measurements. Reductive dissolution experiments were conducted at 23.0±0.5°C and pH 3.35±0.03 in the absence of light under nitrogen. Aqueous [Fe(II)] was measured by the ferrozine assay. High-resolution TEM (HRTEM) revealed that the Hem-7 crystals are pseudo-hexagonal plates and the Hem-30 crystals are rhombohedral. Initial and steady state dissolution rates were determined from batch experiments and compared after surface area (SA) normalization: the initial rates of Hem-7 and Hem-30 are 9.11±2.24 and 4.48±1.62 (10 -7molm -2h -1), and the steady state rates are 1.94±0.53 and 1.29±0.36 (10 -7molm -2h -1), respectively. These results suggest that both initial and steady state rates of Hem-7 dissolution are faster than the steady state rate of Hem-30, although the differences between the steady state rates of Hem-7 and Hem-30 are within one standard deviation. HRTEM observation of individual crystals and aggregates of Hem-7 reveal that this hematite is defect-free and no preferential etching occurred. Additional TEM measurements indicate that previous to dissolution, Hem-7 is present as both dispersed particles and as aggregates. Dispersed particles dissolve initially before aggregates, which influences the dissolution rate. The Hem-30 hematite has nanoscale surface steps and internal defects, and its dissolution initiates from the steps, defects, or sharp edges of the crystals. In addition, HAADF-STEM (high angle annular dark field - scanning transmission electron microscope) tomography was employed to observe the three-dimensional structures of individual particles and aggregates. This three-dimensional tomography reveals that aggregates of nanoparticles dissolve heterogeneously and holes form on the surface of crystals. This study directly shows the importance of size, surface roughness, defects, crystal morphology and aggregation states on dissolution rates of nanoparticles.
AB - Nanoscale iron (oxyhydr)oxide minerals are omnipresent in natural environments and past studies have found that their size, morphology, surface structure, and aggregation state influence chemical reactivity. In this study, we have investigated the influence of these factors on the reductive dissolution of hematite with ascorbic acid using two types of nanoparticles with average diameters of 6.8±0.8nm and 30.5±3.5nm, referred to as Hem-7 and Hem-30, respectively, in this paper. Hematite nanoparticles were synthesized by forced hydrolysis of ferric nitrate and characterized with powder XRD, TEM, and BET surface area measurements. Reductive dissolution experiments were conducted at 23.0±0.5°C and pH 3.35±0.03 in the absence of light under nitrogen. Aqueous [Fe(II)] was measured by the ferrozine assay. High-resolution TEM (HRTEM) revealed that the Hem-7 crystals are pseudo-hexagonal plates and the Hem-30 crystals are rhombohedral. Initial and steady state dissolution rates were determined from batch experiments and compared after surface area (SA) normalization: the initial rates of Hem-7 and Hem-30 are 9.11±2.24 and 4.48±1.62 (10 -7molm -2h -1), and the steady state rates are 1.94±0.53 and 1.29±0.36 (10 -7molm -2h -1), respectively. These results suggest that both initial and steady state rates of Hem-7 dissolution are faster than the steady state rate of Hem-30, although the differences between the steady state rates of Hem-7 and Hem-30 are within one standard deviation. HRTEM observation of individual crystals and aggregates of Hem-7 reveal that this hematite is defect-free and no preferential etching occurred. Additional TEM measurements indicate that previous to dissolution, Hem-7 is present as both dispersed particles and as aggregates. Dispersed particles dissolve initially before aggregates, which influences the dissolution rate. The Hem-30 hematite has nanoscale surface steps and internal defects, and its dissolution initiates from the steps, defects, or sharp edges of the crystals. In addition, HAADF-STEM (high angle annular dark field - scanning transmission electron microscope) tomography was employed to observe the three-dimensional structures of individual particles and aggregates. This three-dimensional tomography reveals that aggregates of nanoparticles dissolve heterogeneously and holes form on the surface of crystals. This study directly shows the importance of size, surface roughness, defects, crystal morphology and aggregation states on dissolution rates of nanoparticles.
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U2 - 10.1016/j.gca.2012.05.008
DO - 10.1016/j.gca.2012.05.008
M3 - Article
AN - SCOPUS:84862687276
SN - 0016-7037
VL - 90
SP - 149
EP - 162
JO - Geochimica et Cosmochimica Acta
JF - Geochimica et Cosmochimica Acta
ER -