A method for preparation and cleaning of uniformly sized arsenopyrite particles
© Parthasarathy et al.; licensee Springer. 2014
Received: 14 May 2014
Accepted: 2 October 2014
Published: 11 October 2014
The oxidative dissolution of sulfide minerals, such as arsenopyrite (FeAsS), is of critical importance in many geochemical systems. A comprehensive understanding of their dissolution rates entails careful preparation of the mineral surface. Measurements of dissolution rates of arsenic from arsenopyrite are dependent on the size and degree of oxidation of its particles, among other factors. In this work, a method was developed for preparation and cleaning of arsenopyrite particles with size range of 15-250 μm. Four different cleaning methods were evaluated for effectiveness based on the removal of oxidized species of iron (Fe), arsenic (As) and sulfur (S) from the surface. The percentage oxidation of the surface was determined using X-ray photoelectron spectroscopy (XPS), and surface stoichiometry was measured using scanning electron microscopy - energy dispersive X-ray spectroscopy (SEM-EDS).
Results indicate that sonicating the arsenopyrite particles and then cleaning them with 12N HCl followed by 50% ethanol, and drying in nitrogen was the most effective method. This method was successful in greatly reducing the oxide species of Fe while completely removing oxides of As and S from the arsenopyrite surface.
Although sonication and acid cleaning have been widely used for mineral preparation, the method described in this study can significantly reduce grain size heterogeneity as well as surface oxidation, which enables greater control in surface and dissolution experiments.
Arsenopyrite (FeAsS (s)) is the most common arsenic (As) bearing pure phase mineral in the earth's crust. It is present in a variety of deposits such as hydrothermal, and magmatic systems and is an important reservoir of arsenic in the subsurface. Due to its common association with gold, it is often discarded as solid waste after gold extraction. The oxidation of arsenopyrite can release As into the environment which has potential environmental and health impacts .
A number of studies - have been conducted that investigate the kinetics of arsenopyrite dissolution with oxidants such as dissolved oxygen and iron, but there is significant variation in reported rates. One of the possible sources of this variation is the lack of a consistent mineral preparation procedure. Differences in mineral preparation can significantly affect grain size distribution as well as affect the extent of oxidation on the surface prior to conducting dissolution studies.
Previous research  indicates that grain sizes can exert significant control over oxidation and dissolution rates. McKibben et al.  determined that 150-250 μm was the most convenient grain size for arsenopyrite dissolution. Arsenopyrite is typically prepared by homogenous grinding of the sample in a mortar and pestle, and then dry sieved to obtain required size fractions. Fine particles have high specific surface areas and their presence in these fractions can cause exaggerated dissolution rates , as well as affect reproducibility of dissolution experiments. Typically, sonication of crushed mineral in ethanol or acetone has been used to remove fines from the surface of sulfide minerals ,,.
Dissolution studies can be further complicated by the presence of oxidized species on the mineral surface, which can lead to erroneous initial rates . Since the dissolution of arsenopyrite is oxidative in nature, oxidized species on the surface could drive subsequent dissolution of arsenopyrite. Acid cleaning has been used extensively in the literature as a method of cleaning sulfide minerals such as pyrite and arsenopyrite, but relies on indirect methods such as initial sulfate release to determine the extent of surface oxidation. Moses et al.  reported the use of a combination of boiling 6N HCl and acetone for surface cleaning of pyrite. The extent of oxidation was determined by monitoring the immediate release of SO42- into solution. In the case of arsenopyrite, McKibben at al.  reported the use of 1.8 N HNO3 for cleaning, while other groups , did not report methods for surface oxide removal. Oxidized iron and arsenic were observed to be removed from the surface of arsenopyrite when it was immersed in an air-saturated acetic acid solution . However, studies on the relative rates of elemental oxidation of arsenopyrite upon exposure to air have shown that As and Fe oxidize at rates faster than S ,, suggesting that measurement of immediate release of sulfate into solution might not accurately reflect the extent of surface oxidation. As a result, there exists a need for direct evaluation of acid cleaning as a viable method for surface oxide removal on arsenopyrite prior to dissolution experiments. Typically, X-ray photoelectron spectroscopy (XPS) has been used to study surface oxidation on many minerals, but studies on arsenopyrite have been limited to vacuum fractured pristine surfaces and surfaces exposed to oxidants.
The objective of this study was to develop a reproducible and effective procedure to generate arsenopyrite particles of a uniform size fraction, free of surface oxides. The specific objectives were to (i) obtain arsenopyrite particles of the size fraction 150-250 μm by removing fines adhering to the surface, and (ii) clean the surface of crushed particles to remove oxide species of Fe, As and S, without altering the stoichiometry of the mineral. The effectiveness of HCl and acetic acid for cleaning the surface of arsenopyrite was evaluated, based on their reported use for this purpose in the literature. The resulting method developed for cleaning the arsenopyrite surface was verified through XPS, particle size distribution analysis, and scanning electron microscopy - energy dispersive X-ray spectroscopy (SEM-EDS).
Results and discussion
Particle size analysis
The effect of drying method on surface oxidation of arsenopyrite
% Oxidation on the surface
In air, 105°C
In air, 25°C
The reported percentages of oxidation were calculated based solely on the fraction of each element that is bound to oxygen. While the extents of oxidation measured from the Fe 2p3/2 and As 3d spectra for a given sample agreed within experimental error, the degree of sulfur oxidized to sulfate measured from the S 2p spectra for the same sample was much less. This has been commonly attributed to the formation of a metal-deficient sulfide species in other studies of the oxidation of pyrite and arsenopyrite surfaces ,,. Further, sulfur on the arsenopyrite surface, oxidizes at a rate much lower than iron and arsenic ,, thereby resulting in a lower extent of sulfur oxidation on the surface.
The results in Table 1 clearly indicate that the drying procedure at room temperature is preferable to drying at 105°C as it limits the extent of surface oxidation. Thus, this procedure was implemented for drying the samples prior to applying various treatments to remove surface oxidation.
Removal of surface oxide species
The results indicate that treatment with the strong acid HCl was more effective in removing surface oxidation than treatment with the weak acid, acetic acid. A higher concentration of HCl was more effective in removing the last traces of surface oxidation over the given treatment time. Within the acetic acid treatments, increasing the treatment time resulted in increased removal of oxidized surface species, but even a treatment time of 20 minutes was insufficient for complete removal of oxidized species.
Only 12N HCl removed all oxidized species of sulfur and arsenic over the given treatment time. However, all four methods failed to remove oxidized iron completely, with 12N HCl being the most effective. For the case of 12N HCl, fitting of the Fe 2p3/2 spectra still indicated some residual surface oxidation. The presence of oxidized iron species has also been observed on vacuum fractured surfaces of arsenopyrite by Nesbitt et al. , who reported that ~17% of the Fe on the surface could be attributed to Fe (III)-(As-S) species. Moreover, the overall higher surface sensitivity of the XPS measurement to the Fe 2p level compared to As 3d and S 2p and/or some small amount of preferential reoxidation of Fe during the sample's exposure to air during its transfer to the XPS instrument could have also resulted in the detection of oxidized iron species, even after cleaning the surface. Comparing the S 2p spectra before and after the HCl treatment, one can see that while all the sulfur oxidized to sulfate has been completely removed by the treatment, the relative percent of metal-deficient polysulfide increased from 5% to 17% of the non oxygen-bound sulfur species. Although metal deficient polysulfide species have been reported in vacuum fractured arsenopyrite , oxidation of samples during procurement and grinding could have resulted in the formation of polysulfides on the surface ,,.
While the 12N HCl cleaning method can be used for other sulfide minerals, using 12N HCl might not be appropriate for acid volatile sulfides (AVS) such as galena (PbS), which dissolve in concentrated HCl .
Further, SEM images of arsenopyrite particles before (Figure 4C) and after treatment with 12N HCl (Figure 4D) did not reveal any significant morphological changes on the surface suggesting minimal change in the specific surface area of the mineral particles due to acid treatment. A comparison between the images depicts an absence of pitting or etching from acid treatment.
Mineral preparation and reagents
Arsenopyrite from Hunan province in China was obtained from Wards Science Inc. (Rochester, NY) in 10 g batches. Each batch was ground to powder using a porcelain mortar and pestle. The mortar and pestle were soaked with 10% HNO3 (w/v) overnight prior to being used for the first time. The powdered arsenopyrite was then dry sieved using 250 μm and 150 μm nylon sieves, which were also soaked in 10% HNO3 (w/v) overnight. The fraction of particles between 150-250 μm was collected and transferred into a plastic tube. From every 10 g batch of mineral, 5 g in the 150-250 μm fraction was obtained in this manner.
ACS reagent grade acids (HCl, acetic acid) were used in all cleaning experiments. All aqueous solutions were prepared using ultra-pure water (18.2 MOhm.cm, Barnstead Nanopure purifying system). Laboratory grade nitrogen (99.9% purity) was used in all experiments for mineral drying.
Removal of fine particles adhered to the surface: particles significantly smaller than the sieved range can be electrostatically bound to the surface of larger particles. Such fines could result in exaggerated measurement of dissolution rates and hence need to be removed.
To remove fines, the particles were sonicated with 50% (v/v) ethanol for 3 minutes using a Branson 5200 sonicator (Branson Inc., Connecticut, USA). Upon sonication, the ethanol phase turned black in color indicating suspended fine particles, and was subsequently decanted. This process was repeated three times and the particles were transferred to a petri dish and dried. Since drying the particles could affect the extent of surface oxidation, two different methods of drying were evaluated: a) drying the particles in air at 105°C for 15 minutes and b) drying the particles in air for 1 hour at room temperature (25°C). The dried arsenopyrite particles were then subjected to XPS analysis and a method for drying was chosen based on the extent of surface oxidation. Limiting the extent of initial surface oxidation enables easier removal of oxidized layers from the surface.
Removal of oxide layers - limited surface oxidation can occur during crushing, sieving, and drying of arsenopyrite. This can impact initial dissolution rate determination, as the rate of oxide phase dissolution can be significantly different from that of arsenopyrite. Further, arsenopyrite dissolution being oxidative in nature could be affected by dissolved oxidized species.
Removal of oxides to the largest possible extent aids in accurate initial rate measurements. Oxides on the surface were removed by washing the arsenopyrite particles with acid.
Methods for cleaning surface oxides on arsenopyrite particles
1N HCl (5 mins)
DIa water (3 mins)
50% (v/v) ethanol (1 min)
12N HCl (5 mins)
DI water (3 mins)
50% (v/v) ethanol (1 min)
50% (v/v) acetic acid (10 mins)
DI water (3 mins)
50% (v/v) ethanol (1 min)
50% (v/v) acetic acid (20 mins)
DI water (3 mins)
50% (v/v) ethanol (1 min)
After cleaning the particles, samples intended for XPS analysis were placed in glass vials, flushed with N2, crimped, and transported in vacuum containers capable of maintaining vacuum of 14.7" Hg for over 24h, (Desi-Vac 700 mL containers, Cole palmer, USA). All samples were analyzed the same day that the cleaning method was applied.
Summary of arsenopyrite preparation method
Arsenopyrite was crushed in a mortar and pestle. Dry sieved to obtain 150-250 μm size fraction.
Sonicated in 50% ethanol and supernatant decanted (thrice).
Dried under N2 at room temperature for 1 hour.
Rinsed with 12N HCl for 5 minutes, followed by water (3 minutes) and 50% ethanol (1 minute)
Dried under N2 for 1 hour.
Particle size distribution
The effectiveness of sonication in removing fines was analyzed by measuring the average diameter of the particles by laser diffraction at Particle Tech Labs (Illinois, USA). Ten grams of sonicated and dried arsenopyrite were shipped in a 15 mL centrifuge tube (Corning USA) for analysis. The particle diameter distribution was calculated on a % volume basis.
XPS measurements were carried out using a PHI 5600ci instrument. The XPS instrument employed monochromatic Al Kα X-rays and the pass energy of the analyzer was 23.5 eV. The arsenopyrite powders were attached to the sample holder using double-sided adhesive, electrically-conductive tape. Percentages of elemental oxidation were calculated from the relative areas of component peaks after the overall peak envelope for a given XPS peak was fitted with the component peaks due to oxidized and unoxidized forms of the element. Elemental concentrations were calculated using sensitivity factors provided by the instrument manufacturer. XPS peak fitting analyses were accomplished using CasaXPS data processing software. Binding energies were referenced to the C 1s peak for adventitious carbon at 284.6 eV.
SEM was used for visual confirmation of arsenopyrite particle size and to evaluate surface composition of the particles. Once a suitable method for cleaning was chosen based on XPS data, arsenopyrite was prepared fresh, stored under vacuum, as previously described, and subjected to analysis within 2 hours of cleaning. The SEM was performed using a Philips XL30 FEG scanning microscope equipped with an SE Everhart Thornley detector and an Oxford INCA EDS with full quantitative composition analysis. The operating conditions were, accelerating voltage 10 kV, spot size 3, and a working distance of 10 mm. The SEM-EDS had a detection limit of 1% by weight.
We thank Drs. J. Alexandra Hakala and Christina Lopano of National Energy Technology Laboratory for their useful comments.
This project was funded in part by the John and Claire Bertucci Fellowship in Engineering, and by the Department of Energy, National Energy Technology Laboratory (NETL), an agency of the United States Government, through a support contract (DE-FE0004000) with URS Energy & Construction, Inc as part of the NETL's Regional University Alliance (RUA). Neither the United States Government nor any agency thereof, nor any of their employees, nor URS Energy & Construction, Inc., nor any of their employees, makes any warranty, expressed or implied, or assumes any legal liability or responsibility for the accuracy, completeness, or usefulness of any information, apparatus, product, or process disclosed, or represents that its use would not infringe privately owned rights. Reference herein to any specific commercial product, process, or service by trade name, trademark, manufacturer, or otherwise, does not necessarily constitute or imply its endorsement, recommendation, or favoring by the United States Government or any agency thereof. The views and opinions of authors expressed herein do not necessarily state or reflect those of the United States Government or any agency thereof.
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