2011 Progress Report: Platinum-Containing Nanomaterials: Sources, Speciation, and Toxicity in the Environment

EPA Grant Number: R833892
Title: Platinum-Containing Nanomaterials: Sources, Speciation, and Toxicity in the Environment
Investigators: Schauer, James J. , Shafer, Martin M. , Toner, Brandy M.
Institution: University of Wisconsin - Madison , University of Minnesota - Twin Cities
EPA Project Officer: Lasat, Mitch
Project Period: February 1, 2009 through January 31, 2013
Project Period Covered by this Report: February 1, 2011 through January 31,2012
Project Amount: $399,406
RFA: Exploratory Research: Nanotechnology Research Grants Investigating Fate, Transport, Transformation, and Exposure of Engineered Nanomaterials: A Joint Research Solicitation - EPA, NSF, & DOE (2007) RFA Text |  Recipients Lists
Research Category: Nanotechnology , Safer Chemicals


Platinum is the archetypal element where chemical and physical speciation is essential for valid toxicology assessments, yet critical basic information on environmental pools, speciation and reactivity is lacking. Anthropogenic platinum emissions to the environment have dramatically risen over the past 2-3 decades and consumptive use, particularly in nano-catalytic applications, is projected to increase. Nano-particulate species of platinum represent a major fraction of total platinum in most primary emissions. Platinum in most primary emissions was thought to be present in relatively benign metal-elemental species; however, evidence is mounting that a portion of the platinum in major sources may exist in more toxic/bioavailable forms and that the speciation of platinum (particularly nano-sized platinum) can change rapidly after release to the environment. Information on environmental levels of the recognized toxic species of platinum (chloroplatinates) is essentially absent. Our research addresses three major questions:
(a) What are the primary sources and environmental receptors of platinum and nano-platinum?
(b) What are the chemical forms of platinum introduced into the environment from current and potential major sources?
(c) How does the speciation of platinum change within specific environmental reservoirs after release?
Our focus is on aerosol-mediated emissions, transport, and exposure in non-occupational settings. Emissions from vehicles (exhaust catalysts [TWC] are a major source of platinum) are being addressed using roadside aerosol and roadway dust sampling. Engine dynamometer experiments were conducted to evaluate platinum emissions from fuel-borne catalysts (FBC). High-volume air samplers are being used to collect ambient aerosols in several urban environments. Concentrations and chemical speciation of platinum in particulate (PM) and “soluble” phases of these samples are being determined with a suite of analytical tools. Synchrotron XAS (sXAS) is applied to solid phases. “Soluble” species, as defined with physiological relevant fluid extractions, are characterized by SF-ICPMS, HPLC-ICPMS, HPLC-MS/MS, ultra-filtration, and ion chromatography. Several parallel strategies are being used to examine the presence of chloroplatinate species in environmental materials. Platinum species transformations are being evaluated in controlled laboratory experiments with both environmental and model samples.
Through our multidisciplinary approach we expect to substantially advance our understanding of the sources, speciation, transformation, and potential human exposures to nano-platinum materials in the environment. We expect to provide some of the first measurements of the recognized toxic species of platinum in environmental media. Vital information on the concentrations and chemical species of platinum in mobile source emissions and important environmental receptors will be provided. Fundamental data on rates of species transformation will be acquired. The chemical speciation and exposure data will enable enhanced assessments of the toxicological relevance of environmental nano-platinum species.

Progress Summary:

1. sXAS and chemical speciation results indicate the presence of a large component of oxidized species of platinum (particularly Pt(IV)-oxide) in emissions from diesel engines burning platinum-amended fuel.
2. sXAS studies of used automobile three-way-catalysts provide strong support for the presence of oxidized platinum species along with evidence for very low concentrations of chloroplatinates (0.5-10 ng/g).
3. Given low platinum concentrations in real-world samples and our current understanding of EXAFS spectra, it will be difficult to distinguish between chlorine bonded with platinum as a chloroplatinate and chlorine associated in a more ionic form.
Synchrotron X-Ray Absorption Spectroscopy (sXAS) is a powerful approach that provides chemical speciation information directly from solids (e.g., engine PM and catalyst materials). In the XANES region of the XAS spectrum, data on the oxidation state of Pt can be obtained, and in the EXAFS spectral region data on nearest neighbor bonding (e.g., O, Cl, S, Pt) can be acquired. At beamline 10.3.2. at LBL-ALS, we performed focused beam (3 µm) platinum XANES/EXAFS in conjunction with detailed x-ray fluorescence mapping of thin-sections of new and used three-way catalysts as well as on engine PM collected from the face of a diesel particulate filter (DPF) from an engine running with platinum-amended fuel. The fine spatial resolution at ALS 10.3.2 enables one to map areas/particles enriched in platinum, identify elemental co-associations, and subsequently perform XAS on those spots. We also now have, on four separate occasions (48 shifts), the latest in October 2011, performed bulk (1000 µm) and semi-focused (250 µm) sXAS at ANL-APS on beamline 20-BM. The significantly higher x-ray flux at the APS permits higher quality XANES/EXAFS spectra on the low concentration (< 100 ppm), relatively homogeneously distributed platinum species in the PM from diesel amended fuel. At ALS and APS, we have collected high quality EXAFS spectra on a large number of platinum reference materials at both the L2 and L3 edges – our library of reference material spectra now numbers 18. These reference spectra are used to fit spectra obtained from our source and receptor samples. The XAS spectra obtained in our November 2010 and October 2011 shifts at ANL-APS confirm our previous findings that a large fraction of the platinum in PM from diesel engines burning platinum-amended fuel is present in oxidized forms, most likely as a platinum (IV) oxide. During the October 2011 beamtime, we implemented a series of sample preparation and data acquisition improvements that resulted in the cleanest and highest quality spectra to date of PM from engines burning platinum amended fuel. These data were subjected to both Linear Least Squares Fitting and first principles EXAFS shell-by-shell modeling. Modeling of these EXAFS spectra, from both fresh and aged samples, indicate that all are well-fit by oxide models. Except for one sample, addition of chlorine to the models does not improve fit.
4. All primary field sampling activities planned for this study were effectively completed. This included:
a.  Two 3-week long road-side atmospheric aerosol sampling campaigns in the Milwaukee metro area, one in August 2010 and another in March 2011. The contrasting campaigns were designed to evaluate the influence of chloride levels on platinum speciation. In addition to large-mass bulk (TSP) samples (collected on 8x10” Teflon sheets), detailed size-fractionated aerosol also was obtained using Cascade Impactors.
b.  Road dust sampling campaigns in Los Angeles, Atlanta, Denver, and Milwaukee. The road dust samples were sieved to create TSP fractions and also resuspended in a dilution chamber and PM10 and PM2.5 fractions pulled off.
Concentrations of TOTAL platinum in the road dusts were highest in Los Angeles (7 sites, 280-720 ng/g), followed by Atlanta (3 sites, 100-380 ng/g), Denver (3 sites, 170-300 ng/g), and Milwaukee (3, sites 70-90 ng/g). In general, the ratios of platinum-group elements (Pt/Pd; Pt/Rh; Pd/Rh) in the road dusts were similar within and between cities, indicating a similar (vehicular) source.
A relatively small fraction of the total platinum in roadside atmospheric aerosol was present in nano-sized (<0.25 µm) particles (10-20%). Particle-size distributions of roadside aerosol platinum exhibit a mode around 1 µm.
5. The fraction of total platinum in particulate matter from diesel engines burning platinum-amended fuel that was extractable with Water and Gambles Saline ranged from 1-2%. The large majority of this pool of platinum was present as truly dissolved species with anionic character dominating (> 80%). Greater fractions of total platinum were extractable in Macrophage Vacuole Fluid (3-4%) and dilute HCl (5-7%), though the speciation was similar. The Water and Gambles Saline solubility of platinum in roadway dusts was significantly lower (0.2%), though substantially higher solubilities were measured in Macrophage Vacuole and dilute HCl solutions (1-2% of Total). The anionic component of the roadway dust extracts was much smaller (< 50%) than measured in diesel PM. The Water and Gambles Saline solubility of platinum in used TWC was very low (0.01%); higher solubilities were measured in Macrophage Vacuole (0.04%) and especially dilute HCl solutions (0.3% of Total). The anionic component of the used catalyst extracts was the smallest of all materials examined. A substantial nanoparticle component of the TWC extracts was observed. Water and Gambles Saline solubility of platinum in roadside aerosol was the highest of all materials examined (10% of total platinum); even higher solubilities were measured in Macrophage Vacuole (20%); however, the soluble fraction in dilute HCl solutions was similar to that in water. The anionic component of the roadside aerosol extracts was at least 50% of the dissolved extractable platinum. The nanoparticle component of the roadside aerosol extracts was minimal.
A detailed chemical speciation scheme was developed to assess soluble, nano, dissolved, and anionic species of platinum in roadway dusts, roadside soils and PM collected from engines burning Pt-amended fuel.
i. Total metal (Pt, Pd, Rh and 45 other elements) content in the particulates is determined by magnetic-sector ICP-MS after complete dissolution of the particulates (microwave assisted acid digestion in Teflon bombs).
ii. A battery of extraction fluids are used to assess the soluble/mobile fraction of Pt (and other elements) in the particulates: (a) high purity water (MQ) is used as a reference fluid, (b) two physiologically relevant fluids - Gambles and a surrogate macrophage vacuole solution, simulate availability to biological systems, (c) 1 N HCl is the preferred matrix for extraction/preservation of chloroplatinate species, and (d) methanol is applied to selected samples to access binding sites sequestered in the hydrophobic soot matrix. Total extractable Pt (and other metals) in each fluid is determined by magnetic-sector ICP-MS, after filtration at 0.22 micron.
iii. Colloidal/nano and dissolved species are physically separated by ultrafiltration at 10 kDa in all extraction fluids, and then each fraction is subjected to SF-ICP-MS.
iv. Anionic species (e.g., chloroplatinates) are physically separated from neutral and cationic species using DEAE Chromatography (and in certain samples, Strong Anion Chromatography – SAX), and each fraction then is characterized by SF-ICP-MS.
v. Soluble ions (nitrate, chloride, sulfate, ammonium) and soluble organic carbon also are measured.
The kinetics of release of platinum (and other metals) from the particulates were examined by time-coarse extractions in each fluid – time points of 2, 6, 24, and 48 hours. Three solid-solution ratios are employed (200, 500, and 2000 mg/L) to ensure that the partitioning of metals to the solids is well characterized.
6. We have developed a method, using HPLC (IC) - SF-ICPMS for speciating chloroplatinates in extracts of source and receptor particulates. A 5 mM K2EDTA solution, while not quantitative in extracting chloroplatinates from environmental materials, does not artifactually produce chloroplatinates and is effective in stabilizing chloroplatinate speciation.
The HPLC-SF-ICPMS chloroplatinate analysis method that we have developed is based on a method published by Nachtigall, et al. [1] and Nischwitz, et al. [2, 3]. The two chloroplatinate species, tetrachloroplatinate (PtCl42-, “Tetra”) and hexachloroplatinate (PtCl62-, “Hexa”) are separated isocratically using a Dionex AG11 guard column containing an alkanol quaternary ammonium stationary phase and a mobile phase consisting of 0.1 M sodium perchlorate/HCl at pH = 1.9, and detected with a magnetic sector ICPMS. The perchlorate anion acts as a counter-ion to the chloroplatinates for this separation. Because this mobile phase is detrimental to most mass spectrometry interfaces, a switching valve and an automated timing program was developed to minimize the amount of NaClO4 introduced to the ICPMS. Using this program, only regions of the chromatogram containing the void, Tetra, and Hexa species are allowed into the ICPMS. We also now have moved to a totally automated HPLC fraction collection protocol, where the regions of the chromatogram noted above are physically collected offline from the SF-ICPMS and analyzed as discrete samples. This gives us the flexibility to run the collected fractions on the SF-ICPMS under further optimized signal/noise conditions. The limit of detection of the instrumental method is 25 parts-per-trillion (ppt) [2 pg injected] in both standard mixtures and in spiked tunnel dust (CRM 723) extracts. A 5-fold further improvement in effective sensitivity (0.4 pg injected, which allows us to characterize chloroplatinates at our target level of 0.1% of total platinum in solids) is achieved using a turbo-vap volume reduction pre-concentration method. Extensive experimental efforts were directed at validating extraction methods for the chloroplatinates from each of three source materials (diesel engine PM, road dust, and bulk cordierite TWC). Extractants examined included (a) EDTA alone (5 and 20 mM), (b) methanolic EDTA (5 different ratios: 10/90, 25/75, 50/50, 75/25, 90/10), and (c) dilute HCl (0.05, 0.1, and 0.5 M). For road dust and catalyst materials, a 5 mM K2EDTA solution, while not quantitative in extracting chloroplatinates from environmental materials, does not artifactually produce chloroplatinates and is effective in stabilizing chloroplatinate speciation; and we are moving forward with this extractant. A 50% MeOH solution with EDTA is more effective in both extracting and maintaining chloroplatinate speciation from diesel PM than other solvent systems examined.
We currently are applying these extraction and analysis methods to many of the source and environmental receptor materials that we have collected.

Future Activities:

All major field sampling activities planned for this study were effectively completed in Years 1 and 2; therefore, only limited additional sampling, in support of the Environmental Transformation Studies, XAS characterization of catalysts, and chloroplatinate sub-studies will be performed.
Another roadside aerosol sampling campaign is scheduled for October 2012 in Atlanta. Sampling sites will be located near the major roadways where road dust was previously collected. Large masses (10’s of mg) of size-fractionated aerosol will be collected using a Hi-Vol impactor, and subjected to detailed chemical speciation.
The primary thrust of our current experimental program is Environmental Transformation Studies. These experiments are being conducted at the University of Wisconsin-Madison Biotron, where well-defined environmental conditions can be maintained and exposures conducted. We are simulating four transformation scenarios (a) neat sample in contact with air, (b) sample mixed 50+50 with NaCl to evaluate a road-salt exposure scenario, (c) a soil burial scenario where samples are mixed 1+9 with a surrogate soil, and (d) suspension in a simulated roadway runoff/soil leachate. Real-world samples that we have collected, including: (1) engine exhaust particulate matter from Pt-FBC-treated diesel fuel, (2) size-resolved roadside aerosol, and (3) size-resolved particulate matter from urban atmospheres, will be subjected to the exposure scenarios under carefully controlled and step-varied conditions of (i) time, (ii) humidity, and (iii) light. Samples are collected/sacrificed at time points of 2, 6, 12, and 24 weeks, and then are subjected to the comprehensive physical and chemical speciation program previously described.
A parallel thrust in Year 3 will be completing and submitting for peer review the manuscripts that currently are being drafted; including (a) Chemical and Physical Speciation of Platinum in Particulate Emissions from Diesel Engines Burning Platinum-Amended Diesel Fuel, (b) Chemical and Physical Speciation of Platinum in Road Dusts and Road-side Atmospheric Aerosols in Urban Environments of the US, (c) Development and Application of a HPLC-IC-SF-ICPMS Method for Determination of Chloroplatinates in Environmental Materials, and (d) Chemical and Physical Speciation of Platinum in Used Vehicle Exhaust Catalysts. Also planned are manuscripts that address (a) environmental transformations of platinum, (b) synchrotron XAS approaches for detection of chlorine-bearing platinum species in environmental materials, and (c) occurrence of chloroplatinate species in the environment.


  1. Nachtigall D, Artelt S, Wunsch G. J. Chromatogr. A. 775 (1997) 197-210.
  2. Nischwitz V, Michalke B, Kettrup A. J. Chromatogr. A. 1016 (2003) 223.
  3. Nischwitz V, Michalke B, Kettrup A. Anal. Chim. Acta. 521 (2004) 87-93.

Journal Articles:

No journal articles submitted with this report: View all 7 publications for this project

Supplemental Keywords:

platinum, speciation, environment, aerosol, chloroplatinate, transformation, synchrotron XAS, physiological extraction, vehicle emissions, platinum-amended fuel

Progress and Final Reports:

Original Abstract
  • 2009 Progress Report
  • 2010 Progress Report
  • Final Report