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University of South FloridaScholar Commons
Graduate Theses and Dissertations Graduate School
2006
Gold mining in a tropical rainforest: Mercurysorption to soils in the mining region of Arakaka-Mathew's Ridge, GuyanaJoniqua A'ja HowardUniversity of South Florida
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Scholar Commons CitationHoward, Joniqua A'ja, "Gold mining in a tropical rainforest: Mercury sorption to soils in the mining region of Arakaka-Mathew'sRidge, Guyana" (2006). Graduate Theses and Dissertations.http://scholarcommons.usf.edu/etd/2564
Gold Mining in a Tropical Rainforest:
Mercury Sorption to Soils in the Mining Region of Arakaka-Matthew's Ridge, Guyana
by
Joniqua A'ja Howard
A thesis submitted in partial fulfillment of the requirements for the degree of
Master of Science in Environmental Engineering Department of Civil and Environmental Engineering
College of Engineering University of South Florida
Major Professor: Maya Trotz, Ph.D. Daniel Yeh, Ph.D.
Nooren Poor, Ph.D.
Date of Approval: September 16, 2006
Keywords: iron oxide, batch equilibrium sorption, cold vapor analysis, THg,TLM
© Copyright 2006, Joniqua A'ja Howard
DEDICATION
This is for my ancestors, grandparents, and the many storms I encountered.
Sankofa!
ACKNOWLEDGEMENTS
“It is God who arms me with strength and makes my way perfect. He makes my feet like
the feet of a deer; he enables me to stand on the heights,…broaden the path beneath me,
so that my ankles do not turn…pursue my enemies and overtake them;.. and crush them
so that they could not rise... “–Psalms 18-32-36-
Also, I must extend my deepest gratitude and appreciation for my major professor, Dr.
Maya Trotz, and my committee members (Dr. Poor and Dr. Yeh) for helping me
formulate my thesis and challenging me throughout this period. Special thanks to my
family, close spiritual cheerleaders (Erlande Omisca and Quenton Bonds), my Bridge to
Doctorate Family, Mr. Benard Batson, and my lab buddies (Melody Nocon, Mike
“Austin” Roe, and Douglas Oti) for all their support during this challenging time. Most
importantly I must thank the National Science Foundation’s Bridge to Doctorate and GK-
12 STARS programs for the financial support.
“Remember this: Whoever sows sparingly will also reap sparingly, and whoever sows
generously will also reap generously.”– 2 Cor. 9:6, NIV. –
i
TABLE OF CONTENTS
LIST OF TABLES............................................................................................................. iii
LIST OF FIGURES .............................................................................................................v
ABSTRACT...................................................................................................................... vii
CHAPTER 1: INTRODUCTION........................................................................................1
1.1 Motivation and Research Objectives ...............................................................1
1.2 Scope of Work and Approach...........................................................................2
CHAPTER 2: BACKGROUND..........................................................................................3
2.1 Introduction.......................................................................................................3
2.2 Mercury and its Health Effects ..........................................................................3
2.3 Mercury and its Uses .........................................................................................5
2.4 Impacts of Artisinal Gold Mining in South America.........................................6
2.5 Mercury Fate in the Aquatic Environment ........................................................8
2.5.1 Mercury Sorption.................................................................................9
2.6 Guyana .............................................................................................................13
CHAPTER 3: MATERIALS AND METHODS ...............................................................17
3.1 Introduction.....................................................................................................17
3.2 Materials ..........................................................................................................17
3.2.1 Glassware .........................................................................................17
3.2.2 Reagents ...........................................................................................17
3.2.3 Kemiron/Sediments ..........................................................................18
ii
3.3 Analytical Procedures ......................................................................................19
3.3.1 Cold Vapor Atomic Adsorption .......................................................19
3.3.2 Scanning Electron Microscopy/Electron Dispersive Spectroscopy....................................................................................21
3.4 Batch Equilibrium Sorption Experiments.......................................................21
CHAPTER 4: RESULTS AND DISCUSSION................................................................26
4.1 Introduction.....................................................................................................26
4.2 Total Mercury Analysis ..................................................................................26
4.3 BET SEM/EDS and XRD...............................................................................28
4.4 Batch Equilibrium Sorption .............................................................................34
CHAPTER 5: SUMMARY, CONCLUSION, AND RECOMMENDATIONS FOR FUTURE WORK..............................................................................42
5.1 Introduction......................................................................................................42
5.2 Summary of Results and Conclusions .............................................................42
5.3 Recommendations for Future Work................................................................44
REFERENCES ..................................................................................................................46
APPENDICES ...................................................................................................................54
Appendix A: Abridged Experimental Results .......................................................55
iii
LIST OF TABLES
Table 2.1: Current regulatory limits and guidelines for mercury set by the US Environmental Protection Agency and the World Health Organization ...........4
Table 2.2: Mercury concentrations in sediment and water samples from different parts of the world. ..............................................................................................7
Table 2.3: Historical background total mercury concentrations..........................................8
Table 2.4: Content of various elements in soils.................................................................10
Table 3.1: Optimal working conditions for Hg determination in sediments using CVAAS............................................................................................................20
Table 3.2: Conditions used for batch adsorption studies (1000 ppb Hg = 0.5E-5M) ...............................................................................22
Table 3.3: Formation constants for Hg2+ species, Log K’s for ionic strength ...................23
Table 4.1: Total mercury concentrations in Matthew’s Ridge/Arakaka area ....................27
Table 4.2: Summary of batch equilibrium sorption studies...............................................36
Table A.1: 100 ppb Hg (Hg(NO3)2) sorption on 0.1 g Pakera Creek sediment (1.1) ..................................................................................................55
Table A.2: 100 ppb Hg (Hg(NO3)2) sorption on 0.1 g Pakera Creek sediment (1.2) ..................................................................................................56
Table A.3: 100 ppb Hg (Hg(NO3)2) sorption on 0.1 g Philip’s Mine tailings (2.1) .....................................................................................................57
iv
Table A.4: 100 ppb Hg (Hg(NO3)2) sorption on 0.1 g Philip’s Mine tailings (2.2) .....................................................................................................58
Table A.5: 100 ppb Hg (Hg(NO3)2) sorption on 0.1 g Kemiron (3.1)...............................59
Table A.6: 100 ppb Hg (Hg(NO3)2) sorption on 0.1 g Kemiron (3.2)...............................60
Table A.7: 100 ppb Hg (Hg(NO3)2) sorption on 0.1 g Kemiron (3.3)...............................60
Table A.8: 1,000 ppb Hg (Hg(NO3)2) sorption on 0.1 g Kemiron (4.1)............................61
Table A.9: 1,000 ppb Hg (HgCl2) sorption on 0.1 g Pakera Creek (5.1)...........................62
Table A.10: 1,000 ppb Hg (HgCl2) sorption on 0.1 g Philip’s Mine (5.2) ........................62
Table A.11: 1,000 ppb Hg (HgCl2) sorption on 0.1 g Kemiron (5.3)................................63
Table A.12: EDS quantification (Arakaka Creek).............................................................64
Table A.13: EDS quantification (Kemiron).......................................................................64
Table A.14: EDS quantification (Philip’s Mine) ...............................................................64
Table A.15: EDS quantification (Pakera Creek)................................................................65
Table A.16: EDS quantification (Pakera Creek (2)) ..........................................................65
v
LIST OF FIGURES
Figure 2.1: (A) Historical trend in nominal and real gold price = 100*(nominal average annual gold price/ average annual US CPI (all items urban consumers, 1982-1984=100). 2006 averaged from January to May). (B) Estimated global mercury use in the world in 2000 for a total of 3,386 metric tons ..............................................................................................6
Figure 2.2: Some of the transformations involved in the cycling of mercury ....................9
Figure 2.3: Depiction of the solid-water interface and sorption interpretation.................11
Figure 2.4: Map of northern portion of Guyana and test site (Arakaka) plus sites where previous studies have been published .................................................14
Figure 3.1: Speciation of 1E-5 M Hg2+.............................................................................24
Figure 3.2: Speciation of 5E-4 M Hg2+.............................................................................24
Figure 3.3: Speciation of 5E-4 M Hg2+ with 0.001M Cl- .................................................25
Figure 4.1: SEM images of Kemiron for particles up to 38 μm in diameter ....................30
Figure 4.2: SEM image of Pakera Creek particles up to 38 μm in diameter ....................30
Figure 4.3: SEM image of Philip’s Mine for particles up to 38 μm in diameter...............30
Figure 4.4: EDS spectra and chemical quantification table for Philip’s Mine tailings..............................................................................................................31
vi
Figure 4.5: EDS spectra and chemical quantification for Pakera Creek............................31
Figure 4.6: EDS spectra and chemical quantification for Kemiron...................................32
Figure 4.7: XRD spectra for Philip’s Mine tailings...........................................................33
Figure 4.8: XRD spectra for Kemiron ..............................................................................33
Figure 4.9: Sediment samples (Kemiron, Pakera Creek, and Philip’s Mine) ....................34
Figure 4.10: Typical standards curve for THg analysis using CVAAS ............................35
Figure 4.11: Hg sorption to 0.5 g/L Kemiron ....................................................................37
Figure 4.12: Hg sorption to 0.5 g/L Pakera Creek sediment .............................................37
Figure 4.13: Hg sorption to 0.5 g/L Philip’s Mine tailings................................................38
Figure 4.14: Hg sorption to 0.5 g/L of soil for 1,000 ppb Hg (from HgCl2) .....................39
Figure 4.15: Hg sorption to 0.5 g/L of soil for 1,000 ppb Hg (from HgCl2 and Hg(NO3)2) .........................................................................39
vii
GOLD MINING IN A TROPICAL RAINFOREST:
MERCURY SORPTION TO SOILS IN THE MINING REGION OF ARAKAKA-
MATTHEW'S RIDGE, GUYANA
Joniqua Aja Howard
ABSTRACT
Gold mining by artisinal (small-medium scale) miners causes an immense amount of
damage to the environment (i.e. soil erosion, mobilization of heavy metals, etc.).1, 2 One
of the most popular gold mining techniques employed by artisinal miners in Guyana is
mercury amalgamation. During the amalgamation process approximately 300 metric
tons/yr 11, 12 of mercury is used. Mercury once in the environment can be transported
through the air, soil, and water column. It is estimated that 90-99% of total mercury
(THg) is associated with the sediment. An understanding of the geochemical conditions
that affect the fate of mercury in soils, which can act as potential sinks or sources for
mercury, can provide solutions for reduced environmental impacts of mercury
contamination.
Local Guyanese agencies have become concerned with the quality of the water, soil,
biota, and human impact in remote locations in the interior of Guyana. Therefore, soil
samples were collected from two local mines in Guyana’s Arakaka-Mathew’s Ridge area.
Two soil samples (Pakera Creek and Philip’s Mine) and a commercially available iron-
oxide sorbent, Kemiron, underwent CVAAS, BET surface area analysis, electron
dispersion spectroscopy, and x-ray diffractometry. THg concentrations for recovered soil
samples were approximately 300 ng/kg. In addition, samples were subjected to batch
equilibrium sorption studies as a function of pH and mercury species/concentration added
viii
as Hg(NO3)2 and HgCl2. All samples showed significant amounts of sorption between
pH 3-9 for 100-1,000 ppb Hg added as Hg(NO3)2. When HgCl2.was added to the batch
reactor containing Kemiron, an iron-oxide surface, the adsorption behavior of Hg2+
decreased. Philip’s Mine solids, characterized as silicon dioxide by BET, had the lowest
surface area (4 m2/g) and sorption when added as Hg(NO3)2 and HgCl2. On the other
hand, Kemiron and Pakera Creek displayed similar sorption behaviors with high sorption
across all pH ranges. This may be due to similar chemistry and larger surface areas.
Surface loadings were 200 mg/kg and 2,000 mg/kg for experiments with 100 ppb Hg and
1,000 ppb Hg, respectively. Further analysis is required to identify the binding
mechanisms between mercury and samples as well as the role of organic matter content
on samples.
CHAPTER 1: INTRODUCTION
1.1 Motivation and Research Objectives
Mercury pollution due to gold mining has been widely studied in the Amazon River
Basin1, which includes Brazil, Venezuela and the Guianas. Most of the mercury
pollution studies have been conducted in Brazil with a very limited amount of research
coming out of the much smaller Guyana (British Guyana). In Guyana there has been an
increase in mercury loading in the environment and a significant expansion in the number
of permits held by artisinal (small- and medium-scale placer deposit mines) that utilize
mercury for gold extraction 2. Not surprisingly, local agencies like the Guyana
Environmental Protection Agency and the World Wildlife Federation Guianas 3 have
become progressively concerned with the quality of the water, soil, biota, and human
impact in these particular mining areas that are remotely located in the interior of
Guyana. An opportunity arose in May 2005 to accompany a team of investigators into
two mining districts in Guyana (Arakaka and Mathew’s Ridge) under a WWF sponsored
project. From that visit, the Trotz research laboratory at USF obtained soil samples from
the area and pursued further studies on those samples. The WWF study also included
hair, water and fish samples, however, these results remain unavailable as the local
agency, the Institute of Applied Science and Technology, has not completed the research
as of June 2006.
The main objective of this research was to determine the sorptive capabilities of the
Guyanese soils located close to small-medium scale-mining operations in the Arakaka
and Mathew’s Ridge region.
1
These soils can act as potential sinks or sources for mercury and an understanding of
geochemical conditions that affect the fate of mercury can inform solutions for reduced
environmental impacts of mercury contamination in mining activities.
1.2 Scope of Work and Approach
A general overview of the work conducted in this research includes the evaluation of soil
samples collected from Guyana’s Mathew’s Ridge and Arakaka mining districts by BET
surface area analysis, electron dispersion spectroscopy, and X-ray diffractometry for soil
characterization. In addition to soil digestion for total mercury content, batch equilibrium
studies were conducted to understand inorganic mercury sorption on the soils from
Guyana and a commercially available iron oxide sorbent, Kemiron. Mercury
quantification was done using cold-vapor atomic absorption spectroscopy (CVAAS).
These batch equilibrium sorption studies were evaluated as a function of pH and mercury
concentration and mercury species (HgCl2 or Hg(NO3)2). Sorption studies assessed the
ability of sediment to uptake mercury concentrations of 100, 200, and 1,000 μg/L.
This thesis is arranged according to the following format:
• Chapter 2, Background. The background describes the mining environment in
Guyana and discusses mercury chemistry and research.
• Chapter 3, Materials and Methods. This section provides information on the
materials used and experimental and analytical methods used for the work done in
this thesis.
• Chapter 4, Results and Discussion. This section presents and discusses the results
of the experimental data.
• Chapter 5, Conclusion. The last section summarizes the research findings and
makes recommendations for future research.
2
CHAPTER 2: BACKGROUND
2.1 Introduction
This chapter provides an overview of mercury pollution and how it relates to small scale
gold mining operations in Guyana. Also reviewed are mercury transformations in aquatic
systems, health impacts, and the laws/regulations governing the usage of mercury.
2.2 Mercury and its Health Effects
Located on the periodic table as element number 80, mercury is a transition metal which
exists at room temperature as “liquid silver”, known in Latin as hydragyrum. It is both a
natural (e.g. volcanoes) and anthropogenic (e.g. mined ore) contaminant that causes
deleterious human health effects including impaired mental function, neurological
disorders and kidney damage. It is a transition metal commonly found in three oxidation
states (Hg(0), Hg(I), and Hg(II)) and is unique because its elemental state can vaporize at
room temperature. Mercury can transform into methylmercury, the most toxic form
known. Bioaccumulation and biomagnification of methyl mercury occurs to a relatively
high extent in aquatic systems 4-6, making fish consumption the leading route of human
exposure. As a result, United States Environmental Protection Agency (USEPA)
recommended surface and drinking water limits are 12 ng/L and 2000 ng/L total
inorganic mercury, respectively. Table 2.1 lists some guidelines/regulatory limits
currently in effect for mercury.
3
Unlike xenobiotics, mercury is found naturally in the environment and does not degrade
over time, but rather bioaccumulates and biomagnifies. Mercury bioaccumulation
usually occurs in the fatty tissues of fish and is largely magnified in large predatory
species such as salmon, shark, and king mackerel. According to the 2001 USEPA Fish
Advisory warning, about 90% -100% of adult fish contain methylmercury, which
accumulates in the fish muscle bound to proteins. In Minamata, Japan over 3,000 people
suffered from physical deformities, emotional disorders, and oftentimes death due to the
Chisso (“Nitrogen”) Corporation’s release of mercury into the Minamata Bay. The
Chisso Corporation, a chemical manufacturing plant, released approximately 27 tons of
mercury-laced waste into Minamata Bay from 1932 to 1968 where the local diet included
the daily consumption of fish from the bay. As a result of excessive consumption of
mercury-laced fish, residents began to develop signs of methylmercury poisoning, which
became known as “Minamata Disease”.
Table 2.1: Current regulatory limits and guidelines for mercury set by the US Environmental Protection Agency and the World Health Organization.
USEPA WHO Drinking Water MCL (μg/L – inorganic Hg) [4] 2 67 Recommended Surface Water (ng/L) 12 Permissible Hair (μg/g) 11.1 10-208 Urine (μg/g) below 10Fish (μg/g) dry weight (fish-type dependent) 0.5* 2.57
*Same for USFDA
According to the EPA and WHO, consumption of fish containing methyl-mercury should
be limited to an intake of less than 1 ng/g and based on three factors: (1) fish size and
type, (2) regular dietary intake, and (3) location. The agencies recommend that pregnant
woman and children reduce their intake of mercury-laced fish due to mercury’s ability to
be a neurotoxin.
4
2.3 Mercury and its Uses
Various physical, chemical and biological processes influence mercury speciation and
transfer between soil, water, and air and atmospheric deposition has been identified as the
main route of aquatic mercury contamination in non-mining areas of temperate and cold
regions where the bulk of scientific research has been conducted to date. Difficulties still
remain in understanding global inputs to localized systems due to lack of data and
understanding of complex processes governing mercury transformation and emission 9, 10.
In 1995, estimated global anthropogenic contributions to atmospheric mercury emissions
were 2,200 metric tons/yr with power plants being the largest contributor 11 and artisinal
gold mining next with a reported 300 metric tons/yr 11, 12. In terms of use, artisinal gold
and silver mining use nearly 20% of the 3,386 metric tons of mercury produced per year;
batteries and chlor-alkali processes account for 32% and 24% 13 (Figure 2.1). There is
great variation on these estimates because of difficulties with accounting and lack of
enforcement and regulations in some countries. Figure 2.1 depicts the historical trend on
the price of gold and distribution for various processes.
Artisinal gold mining, also referred to as small- to medium- scale mining, describes
mines that use extremely simple (mercury used as an amalgam with no proper processes
regulating releases to the environment) methods for gold recovery from various sizes of
land throughout the world. Mercury has been used for centuries to recover gold and
recent mining activities depend even more heavily on it since most gold is now found in
the very fine fractions of ore. The popularity of mercury use in artisinal mining derives
from its affordability, availability, simplicity of use and lack of regulations governing use
and disposal14. These mines employ an estimated 11.5 to 13.2 million people either
directly or indirectly, in 55 different countries15. These numbers and the use of mercury
will likely increase as gold prices continue to rise and other alternatives for livelihood
and cleaner, affordable processes are not developed. China and Indonesia account for the
bulk of mercury emissions from gold mining whilst approximately 10-30 tons per year
come from countries like Brazil and Venezuela16. The tropical rainforests in the Amazon
5
represent one of the world’s most biodiverse environments that is currently under threat
from artisinal gold mining, deforestation and industrialization.
Figure 2.1: (A) Historical trend in nominal (www.goldprices.com/Goldhistory.htm accessed 7/15/06) and real gold price = 100*(nominal average annual gold price/ average annual US CPI (all items urban consumers, 1982-1984=100). 2006 averaged from January to May) 17. (B) Estimated global mercury use in the world in 2000 for a total of 3,386 metric tons 13.
2.4 Impacts of Artisinal Gold Mining in South America
The typical process used in artisinal mines begins with hydraulic crushing of ore. The ore
is then passed over a sluice box containing a mat to trap gold particles, which are then
recovered by mercury in an amalgam. The amalgam is heated to vaporize the mercury to
recover gold. Though retorts exist for capturing mercury, they are not widely used by
miners. The bulk of studies to date have been conducted in Brazil where mercury
releases from deforestation and industrialization compound the difficulties in estimating
individual sources. Only recently has more research been done in French Guiana,
Suriname and Guyana, which have significantly less inputs from deforestation. Tables
2.2 and 2.3 show some of the sediment, soil and water concentrations found in the
literature.
6
High levels of mercury in indigenous populations of the Amazon basin in Brazil and
Guyana have been reported 18 and linked to the consumption of fish, their primary protein 19. With the exception of disaster areas, hair mercury concentrations of vulnerable groups
(women of reproductive age) in the Amazon are amongst the highest in the world 18.
Table 2.2: Mercury concentrations in sediment and water samples from different parts of the world.
Sediment Unfiltered Water Location Hg 20, 21 (ng/g)
Methyl Hg (ng/g)
Hg (ng/L)
Methyl Hg(ng/L)
Artisinal Au mines, Guyana*22 Artisinal Au mines, Suriname 23 mine wastes streams below mines uncontaminated baselines Amazon basin 24-26 streams affected by mining upstream from mining Antartica streams and lakes Slovenia Hg mine 27 streams affected by mining upstream from mining28 Worldwide background rivers and lakes
5-1200
5.5-200 110-150 14-48
24-406 67-93
1-219 -
-
<0.02-0.83 1.2-1.4
0.03-0.08
0.07-1.9 -
<1 – 0.49 -
-
11-930 -
6.4-10
2.9-33 2.2-2.6 0.27-1.9
18-322
<3 0.1-3.5
-
0.05-3.8 -
0.08-0.28
0.2-0.6 -
0.019-0.33
18-60 0.6 -
*samples collected for this study in May 2005.
Other indigenous populations of the region, e.g. the Maroons in Suriname, also showed
high levels of mercury in urine, which was correlated with proximity to mining activity29.
Studies in Brazil, Suriname, and French Guiana show that piscivorous fish have the
highest mercury concentrations 30-33 and that concentrations increase as a function of
rivers potentially affected by gold mining or industrial sites 31, 33 31. In Suriname,
researchers found that increased turbidity due to mining activities resulted in a layer of
finer particles (< 100 μm) on river sediments which may contribute to negative effects on
local fish populations 34. The turbidity in rivers close to artisinal gold mines in Guyana
and Suriname was also linked to higher mercury concentrations 22, 34. In Guyana, higher
mercury concentrations were found downstream from mining, but researchers could not
tell whether mercury contamination was caused by current amalgamation use or whether
7
it is actually mobilized from the ore itself 2, 22. Whilst these studies provide vital
information on the extent of contamination and the form of contamination based on
spectroscopic or sequential leach analysis, they provide limited information on the
lability, reactivity, and bioavailability of the mercury found.
Table 2.3: Historical background total mercury concentrations.2 Hg Concentrations within various media in mining locations within the humid tropics of
South America Location/media Hg range Reference
Channel sediments (ng/kg) Global background 70 (mean) Turekian, 1971 Poconé area, Brazil 23-198 Von Tümpling et al., 1995 Madiera River, Brazil 50-280 Pfeiffer et al., 1991 Madiera River, Brazil 30-350 Malm et al., 1990 Mazaruni River (Bartica), Guyana 77 (mean) Miller and Lechler, 2003 Essequibo River (Bartica), Guyana 42 (mean) Miller and Lechler, 2003
Soils (ng/kg) (*Ferralitic flood plain soils*) Background 20-50 Pierce et al., 1970 French Guiana 122-318 Rouletand Lucotte, 1995 Madiera River, Brazil 27-54 Malm et al., 1990 Madiera River, Brazil 30-180 Pfeiffer et al., 1991 Madiera River, Brazil 232-406 Lechler et al., 2000 Mazaruni River Basin (Bartica), Guyana 5-83 Miller and Lechler, 2003 Essequibo River Basin (Bartica), Guyana 44-228 Miller and Lechler, 2003
Water (ng L-1) Global Background 1-3 Gustin et al., 1994 Poconé area, Brazil <0.040b Lacerda et al.,1990 Madeira River, Brazil <40-9970b Malm et al., 1990 Madiera River, Brazil 20.0-510 Pfeiffer et al., 1991
b - prior to the use of ultra-clean laboratory procedures
2.5 Mercury Fate in the Aquatic Environment
Various chemical (e.g. sorption, precipitation, photoinduced volatilization) and biological
(methylation or demethylation) processes influence the speciation of mercury in aquatic
systems and extensive research has been done using both model and real conditions to
understand them and the few examples given next just barely capture the complexities.
Some of these processes are depicted in Figure 2.2 and are discussed further in the next
few paragraphs. Gaseous mercury compounds in the atmosphere deposit into the
8
hydrosphere by precipitation or wet deposition (rain, snow, sleet, hail, or mist),
particulate deposition and vapor adsorption (dry deposition), resulting in increased levels
of mercury. Once in the water compartment, mercury undergoes biogeochemical and
photo-oxidation transformation. Mercury is distributed between chemical species
including inorganic divalent mercury (II) and organic mercury (methyl-mercury –
CH3Hg). The dominant species include HgCl2, HgCl42-, Hg2+, Hg, and Hg species sorbed
onto mineral oxides, and organomercury species35. Mercury also forms solid HgS(s)
which is usually, but not always, found under reducing environments (either in sediment
or in biofilms in water column).
Wate
Hg0 (g) Algae
Bacteria CH3HgHg(IIBacteria
Hg(II)- particle
MeHg- particle
Hg- colloi
MeHg-colloi
Air Hg0 (g) Hg(II)
Sunlight
Sediment CH3Hg+Hg(II)Bacteria
HgS
Phyto- plankton
Fish
Zoo- plankton
Figure 2.2: Some of the transformations involved in the cycling of mercury36.
2.5.1 Mercury Sorption
According to Lindsey37 surface sediments in aquifers, lakes, and rivers contain metals in
particular iron and aluminum as well as silica which represent the most abundant mineral
oxides (Table 2.4). Mineral oxides play an important role in the speciation of mercury.
Mineral oxides (e.g. iron and aluminum oxides like goethite and gibbsite respectively)
form amphoteric surface groups when in contact with water. By definition, amphoteric
groups can have positive, negative or neutral charges along the surface/water interface
9
and can accept or lose protons depending on the pH of the solution. The behavior of the
surface/water interface has been modeled using various surface complexation models.
These empirical models include the Constant Capacitance (CC), Diffuse Double Layer
(DD), CD-Music (CD-M), and triple layer (TLM) models. Figure 2.3 uses the triple layer
model to represent a mineral oxide surface showing the different types of surfaces
charges. In this model, the o-plane, that closest to the mineral oxide surface, contains the
amphoteric surface functional groups (XO-, XOH+, XOH), where X is the main ion to
which the surface functional group is associated (e.g. Fe, Al, Si).
Table 2.4: Content of various elements in soils 37.
Metal Selected Average for soils (ng/g) Common Range for Soils (ng/g) Al 71,000 10,000-300,000 Fe 38,000 7,000-550,000 Mn 600 20-3,000 Cu 30 2-100 Cr 100 1-1000 Cd 0.06 0.01-0.70 Zn 50 10-300 As 5 1.0-50 Ni 40 5-500 Ag 0.05 0.01-5 Pb 10 2-200 Hg 0.03 0.01-0.3
10
Figure 2.3: Depiction of the solid-water interface and sorption interpretation.
Therefore, under acidic conditions (or below the pKa of the mineral oxide) the overall
number of positively charged surface sites would increase while under more alkaline
conditions (above the pKa of the mineral oxide) the positive sites would diminish and
vice versa would occur for negatively charged surface sites. Sorbing ions can lose their
spheres of hydration and form a strong covalent bond with the surface in the o-plane (e.g.
SOHg) or they can retain their spheres of hydration and form electrostatic bonds with the
surface in the β-plane (e.g. SO-…..Hg2+). Ions in the diffuse layer and further away from
the surface do not form any electrostatic or covalent bonds with the surface.
Mercury (II) sorption to clays 38, 39 and mineral oxides of iron 40-44, aluminum 40, 42, 45,
and silicon, some of the most common sediment constituents,45-47 typically increases as a
function of pH until it reaches a maxima then decreases in the higher pH regions. Methyl
mercury sorption to goethite and kaolin, on the other hand was found to be much lower
than inorganic Hg(II) sorption 39. The presence of ligands (e.g. chloride, sulfate,
phosphate), other heavy metals (e.g. Ni(II), Pb(II)), and/or organic matter can influence
mercury sorption to mineral oxide surfaces through various processes including
11
competition for surface sites, changes in the surface charge, formation of ternary surfaces
and formation of more stable aqueous complexes 42, 44-48.
In most sediments and natural waters, natural organic matter (NOM) can be found. NOM
consists of carbon-based polyligands with various functional groups including carboxylic
and thiols. Natural organic matter is known to form extremely strong complexes with
mercury 49-51, thereby affecting desorption kinetics from mineral oxides and even
bioavailability 52, 53. Mineral oxide surfaces have been functionalized with synthetic
organic acid to increase the removal of mercury from aqueous solutions 54. These effects
vary, however, depending on the biogeochemical conditions, the form of mercury, the
site and the type of natural organic matter (NOM). For example, fulvic acid, the
hydrophilic fraction of NOM, increased mercury sorption on goethite 41, but decreased
sorption of both Hg(II) and methyl mercury from kaolin 39. NOM has different
functional groups (e.g. carboxylic, phenolic, thiol) that play important roles in
complexing mercury thereby causing a distribution of binding affinities 55, 56.
Methylation and demethylation of mercury can occur via abiotic and microbial pathways 55. Researchers found that dissolved organic matter (DOM) influenced the abiotic, photo-
induced methylation rates of mercury 57. Recent studies on mercury volatilization (to
Hg(0)) found that the presence of NOM decreased volatilization in aqueous solutions, but
that mercury volatilization in real lake samples was significant in sunlight 58.
Nanoparticles like iron oxides may play a major role in the transport of heavy metals in
natural systems 59. Indeed, mercury concentrations downstream of Surinamese and
Guyanese artisinal gold mines were positively correlated with turbidity and the finer
fractions of suspended solids 22, 23. In fact, the majority of the mercury in the Guyanese
samples, including depth profiles from unmined ore, was associated with organic matter 22. This is not surprising given the high forest cover of this area. Based on the literature
review one would expect that the combination of high organic matter and suspended
tailings to have a significant effect on the processes governing mercury speciation and
transport close to artisinal mines.
12
2.6 Guyana
Guyana (located on the north east coast of South America and bordered by Brazil,
Suriname and Venezuela) more closely resembles the English-speaking islands of the
Caribbean with respect to history, language, and culture than its South American
neighbors. It is 214,970 km2 with a population of 765,283 the majority of whom reside
in the coastal area and in poverty 60, 61. Many of Guyana’s indigenous peoples
(Amerindians) reside in the interior regions of the country and are dependent upon the
natural environment for survival and economic resources. The main activities include
manicole palm harvesting, logging, subsistence farming and activities associated with
gold mining. Gold mining has been carried out in Guyana for over 100 years 60-63. The
artisinal gold miners as well as gaimperos or pork knockers, illegal miners, use simple
extraction techniques to quickly recover gold from placer (alluvial, colluvial, or elluvial)
deposits such as land dredging, simple panning techniques, or amalgamation. In the
Barima/Waini area of Region 1, where natives of the Arawak, Carib, and Warau Tribes
reside, gold mining is carried out using the mercury amalgamation process 61.
In Guyana, artisinal gold miners make up approximately 95% of all the miners while the
remaining 5% are from large scale operations. In the large-scale mining sector, miners
use sophisticated equipment and cyanide (HCN) to extract gold from ore. In particular
large scale companies such as OMAI Gold LTD. located in Region 8 utilizes cyanide.
This method of extraction in mining is preferred due to its higher yield of gold recovery
than by the mercury amalgamation. However, due to the economical factors, limited
technology, and easy availability, small-scale miners use elemental mercury.
13
Figure 2.4: Map of northern portion of Guyana and test site (Arakaka) plus sites where
previous studies2,22 have been published.
Figure 2.4 provides a map with the location of the site (Arakaka) plus two rivers for
which the work of the Mazaruni22 and Potero22 have been published. Previous sampling
for mercury in the Wai Wai district, at the most Southernly part of Guyana (not shown on
Figure 2.4) revealed that the Amerindians there had the highest mercury hair
concentrations of a range of Guyanese; fish concentrations were at WHO levels and they
consumed five meals of fish per day 64. The WWF conducted studies at the two gold
mining sites in Guyana, Isseneru, located off of the Mazaruni River (1997, and 2000 65),
Mathew’s Ridge (2005, data not processed as yet) and Arakaka (2005). Isseneru is an
Amerindian village where over 90% of residents surveyed had greater than 14 μg/g hair
concentrations 65 (recommended USEPA permissible limit is 11 μg/g). Singh65, 66
reported that in a total of 168 fish samples collected from Guyana’s Kurupung and
Isseneru areas the average concentration of mercury was 0.315 and 0.928 ng/g THg
which exceeds the United States Food and Drug Administration guidelines limits of 0.5
ng/g (Table 2.1). In addition, Singh66 correlated that elevated levels were due to average
local dietary fish consumptions being 3-4 times per week as well as an association with
14
mercury emanating from the natural environment. Apart from the extensive sediment
sampling that was done along the Mazaruni and Potaro Rivers (indicated on Figure 2.4),
further studies on human levels of contamination and fate of mercury and source of
mercury are obviously needed in Guyana.
Region 1, commonly known as the Northwest district, contains the towns of Arakaka and
Mathew’s Ridge. Arakaka and Mathew’s Ridge cover a land area of approximately
0.0084 km2. This zone is geologically underlain by Precambrian rocks and a 0.001 km2
section of a greenstone belt, an area underlain by metamorphosed volcanic and
sedimentary rocks that contain chlorites, which borders the Iroma and Waini Rivers.
Within Arakaka and Mathew’s Ridge there are or were several industries that include
manganese mining, diamond drilling, and gold mining 63. However, the dominant
commerce today is gold mining. Arakaka is the location of small- to- medium scale gold
mining, and many miners and their families reside in the nearby town of Mathew’s
Ridge. Residents within this area are dependent on the natural water ways for the
collection of fish, the principle source of protein. Drinking water sources include rain
catchments, upstream springs, and river water. A survey done by the WWF-IAST team
in 2005 identified the main sources of drinking water for Arakaka as the Barima River
and rain water.
Mercury amalgamation is the process by which gold is extracted from ore via the usage
of liquid mercury. With a legal mining workforce of roughly 11,000, Guyana’s small
scale mines use the following conventional gold mining process: (1) tree removal by
logging, (2) land dredging or the use of hydraulic pressure to extract alluvial deposits,
sediment that have been settled by water, (3) collection of ore placed on a sluice box for
manual or mechanical gravitational agitation to settle gold deposits, (4) addition of Hg to
the final concentrate (settled gold/ore deposits) that has been shaken off of sluice mats ( It
has been estimated that for every 1 kg of concentrate there is 14 grams of mercury
required to form an amalgamate 67 or oftentimes approximately 30 grams of mercury is
rubbed off on the final concentrate retained on the sluice mats, 63 which is considered an
15
illegal mining practice); (5) followed by a simple panning technique that washes excess
sediment particles from ore to the final recovery process or roasting technique.
Controversy does exist over whether mercury contamination in the Amazon is due to
burning of forests (the ferraltic soils have high background mercury concentrations),
mobilization of ore during mining, input of mercury from amalgamation processes or
atmospheric deposition (with a non- localized mercury source). Atmospheric deposition
has been identified as the main source of contamination, especially to remote areas of the
world 68. In an attempt to model mercury concentrations in the Florida Everglades
researchers found that atmospheric deposition played a major role and noticed that
mercury concentrations increased as a function of the amount of precipitation 9. Few
studies have attempted to measure atmospheric deposition rates in the Amazonian region 69 and mercury concentrations downstream from mining have always been lower than
upstream concentrations suggesting that atmospheric deposition is not as significant as
mining in these areas 21. The literature suggests that higher mercury concentrations are
found downstream from artisinal mines and are directly linked with fines fractions 22, 34.
16
CHAPTER 3: MATERIALS AND METHODS
3.1 Introduction
This chapter describes the materials and methods used in this thesis. It provides a detailed
description of the experimental and analytical procedures used.
3.2 Materials
3.2.1 Glassware
All glassware was washed with a 10% Liquinox detergent and rinsed with MilliQ water
prior to soaking in 1 N NaOH. After one hour glassware was rinsed with MilliQ water
and soaked in 10% HNO3 for an additional hour. The glassware was then rinsed multiple
times with MilliQ water again and allowed to air dry before usage.
Polycarbonate reactor vessels and 10 mL polycarbonate centrifuge tubes were cleaned
separately in a similar fashion as glassware except a q-tip was used to scrub the
containers free of remaining particulate matter and acid and base concentrations were an
order of magnitude lower. All rinse exercises were conducted three times before
proceeding.
3.2.2 Reagents
Mercury stock solutions were prepared in 100 mL glass volumetric flasks by dissolving
Fisher Brand mercuric chloride (M168-100) or mercuric nitrate in a 5% nitric acid
solution. Concentrations of the Hg stock solutions were measured against a calibration
curve prepared using cold vapor atomic absorption of mercury standards. Mercury
17
calibration standards of 5, 10, 20, 30, 50, 70, and 100 ppb (μg/L) were made using a
10,000 ppm (mg/L) mercury stock solution in 5% nitric acid from CentriPrep that was
diluted with 5% hydrochloric acid.
All solutions (slurries and standards) had background electrolyte concentrations of 0.1 N
NaNO3 (Fisher Brand Certified ACS sodium nitrate crystals (S343-500)).
The pH of slurry was varied using 0.1 N NaOH and 0.1 N HNO3. Both acid and base
were standardized using standard methods. MilliQ water was used for all experiments
and analysis.
Acid and reductant solutions for cold vapor atomic absorption analysis were 5% HCl and
10% w/v stannous chloride (LabChem Inc LC25180-1), respectively. A bulk volume of
5% hydrochloric acid solutions were made with 32% w/v HCl (Fisher) and diluted with
MilliQ water. Bulk solutions were stored in 1 L Nalgene high density polyethelyne
bottles.
3.2.3 Kemiron/Sediments
As described by Lindsey37 soils in the environment are principally composed of
aluminum, iron, or manganese oxides. Kemiron, a commercially available iron hydroxide
material was used as a model iron oxide. Kemiron was obtained from Kemiron
Company, U.S.A. It is highly porous with pore sizes ranging from 0.003 μm to 328 μm
and a particle diameters of less than or equal to 600 μm. This commercially available
iron hydroxide material is commonly used as an absorbent in water and waste water
treatment plants. Its principal benefit is to remove turbidity, reduce BOD/TOC/DBP,
precipitate phosphates, condition sludge, reduce bacteria, remove heavy metals, as well
as provide odor and corrosion control.
18
Sediment samples were collected from the Arakaka/Mathew’s Ridge region of Guyana in
May 2005 by the Institute of Applied Science and Technology (IAST) under a project
funded by the Guyana WWF office. These samples were collected in HDPE containers
and included the top 10 cm of sediment from the bottom of the water body tested. They
were stored on ice until airlifted to the IAST laboratory. Once there they were air dried
on filter paper, ground in a mortar and placed in doubly-bagged plastic storage bags.
They were then shipped to the laboratory at USF where they were stored in a freezer until
further use. The Philips Mine Tailings sample was collected by researchers at USF
during the same time period from the tailings pond right under a sluice box at a mine in
Arakaka. The sample was was taken from the surface and placed directly into a sealed
plastic storage bag.
Kemiron and selected sediment samples were ground using a mortar and pestle and
sieved using ASTM-E11, a stainless steel sieve of mesh size 400 (< 38 μm). The sieved
fraction less than 38 μm was stored in doubly sealed plastic storage bags in a sealed
HDPE container. Size fractions of < 38 μm were selected for batch adsorption studies to
decrease equilibration times. A five-point Braunauer, Emmett, and Teller (BET) surface
area analysis was done on Kemiron and selected soil samples using a Coulter SA2300
Surface Area Analyzer. The Kemiron and soils were dried at 80 oC for 18 hours and
outgassed with helium at 80oC for 3 hours. XRD testing was based on particle size
fractions of < 38μm while utilizing the back loading technique.
3.3 Analytical Procedures
3.3.1 Cold Vapor Atomic Adsorption
The Varian 240FS-AAS coupled with a Varian VGA77 attachment were used for the
mercury cold vapor analysis technique also known as cold vapor atomic absorption
spectroscopy (CVAAS). CVAAS analysis was used to determine total mercury
concentrations, THg, in sediment samples.
19
Mercury speciation was not conducted in this study. Before samples were analyzed using
the manual CVAAS technique, all samples were acidified to 0.5% HCl.
Due to the analytical sensitivity when testing for trace levels of mercury extreme care
was exercised. Therefore the capillaries for the acid, reductant, and sample lines of the
continuous vapor flow VGA77 were adjusted to an uptake rate of 1 mL/min, 1 mL/min,
and 8 mL/min, respectively, and a mercury flow-through cell was attached to the Mark V
burner head of the Varian 240FS. Optimal working conditions for the Varian 240FS-
AAS equipped with a VGA77 are outlined in Table 3.1.
Table 3.1: Optimal working conditions for Hg determination in sediments using CVAAS.
Parameters (Varian 240FS) Wavelength (nm) 253.7 Slit Width (nm) 0.5 Lamp Current 4 Integration time (s) 3
Vapor Generator (VGA 77) Acid uptake tube (mL/min) 1 Reductant uptake tube (mL/min) 1 Sample uptake tube (mL/min) 8 Argon* or Nitrogen Gas 99.99% pure Perimissible pressure range*** 43-57 psi
Reagents Usage
5% Hydrochloric Acid, (from concentrated) Acid Line, Reagent Water*, Preservation*
20% (w/v) Stannous Chloride Reductant Line 5% Nitric Acid, concentrated** Reagent water, preservation Notes: * - used in this study ** - suggested (Varian, 1985) *** - recommended pressure is 50 psi
20
The calibration standards for the CVAAS technique were prepared from a 1,000 mg/L
(10-6 μg/L) stock solution manufactured by CentriPrep. Calibration standards of 5, 10, 20,
30, 50, 70, and 100 μg/L were prepared fresh daily. The detection limit for Hg using the
VGA77 and 240FS was 2 μg/L (ppb).
3.3.2 Scanning Electron Microscopy/Electron Dispersive Spectroscopy
The Hitachi SEM Model 4105S was used to observe surface characteristics of sediment
samples. Working conditions for the SEM were between 20 to 17 KeV to reduce the
amount of particle charging at the surface while under a high pressure vacuum of 90
torrs. Sample size fractions of < 38 μm for Philip’s Mine Tailings and Kemiron were
used. To prepare samples for analysis by SEM a small strip of carbon tape was adhered
to the surface of the metal mounting plate. Next, soil samples were distributed evenly on
to the surface of the carbon tape using a pair of metal tweezers then inverted/lightly
tapped to ensure that there were no lose particles. Following procedures outlined in the
SEM/EDS protocol distributed by the Material Science Research Center at the University
of South Florida samples were carefully loaded into the SEM for analysis.
3.4 Batch Equilibrium Sorption Experiments
The batch equilibrium experiment was setup by acid washing a 250-mL Nalgene
polycarbonate reaction vessel with a screw cap and drilled holes for easy insertion of
electrodes and sample ports. Background electrolyte solution of 0.1 N sodium nitrate
(Fisher Brand Certified A.C.S. crystals, Cat. # S343-500) and approximately 0.1 g of soil
were mixed to form a slurry in the polycarbonate vessel. Then the initial pH of the
slurry was analyzed, then the vessel was covered with parafilm and the slurry was
allowed to equilibrate overnight at room temperature, 25˚C. A Teflon magnetic stir bar
was used to continuously stir the slurry overnight. After equilibration, 8 mL of the slurry
were pipetted into a 10-mL Nalgene test tube with screw cap. This sample represented
the initial background mercury concentration (Cblank) and the value was subtracted from
all other concentrations found after mercury addition. The stock mercury solution was
21
then added to give a total added concentration, Cintial. The pH was adjusted to varying pH
values of 3-10 8-mL samples collected at. pH adjustments with 0.1 N NaOH and 0.1 N
HNO3. Once all samples were collected they were placed on an end-over-end shaker for
24 hours to equilibrate. After the 24-hour batch reaction on the end over end Lab Quake
Shaker, samples were analyzed for pH using an Orion Ross 8103BNU pH electrode and
the Orion Duo 940A pH meter. Samples were then filtered using a 0.1 μm disposable
syringe filter, acidified to 0.5% hydrochloric, acid and analyzed for Hg by CVAAS. This
represented the amount of mercury remaining in solution, Csolution.
The amount of mercury removed during the experiment was calculated from:
% removed = [Cintial – Cblank – Csolution]/Cintial
All waste materials were discarded in a double-sealed plastic storage bag following
disposal instructions established by the University of South Florida’s Environmental
Health and Safety department. Equilibrium batch sorption experiments were done on
three solid samples (Kemiron, Pakera Creek, and Philips Mine) at varying mercury
concentrations of 100, 200, and 1,000 ppb (µg/L). The following batch adsorption
studies were conducted on solid samples:
Table 3.2: Conditions used for batch adsorption studies (1000 ppb Hg = 0.5E-5M).
Sample [THg] (made from Hg(NO3)2)
[THg] (made from
HgCl2
Background Electrolyte
Particle size (μm)
Kemiron 100, 1000 ppb 1000 ppb 0.1N NaNO3 < 38 Philips Tailings 100 ppb, 200 ppb,
1000 ppb 1000 ppb 0.1N NaNO3 < 38
Pakera Creek 100 ppb, 1000 ppb 1000 ppb 0.1N NaNO3 --
Experiments were also conducted using solutions of Hg(NO3)2 and HgCl2 at 0.1 N
NaNO3 in the absence of any solids.
22
This was used to provide information on the amount of mercury that could be sorbed to
the surface of the container and filter or photovolatilized during the experiment. These
control experiments resulted in less than 5% removal of mercury. Most experiments
were duplicated.
Table 3.3 provides formation constants that were used to determine Hg speciation under
experimental conditions used in this thesis assuming that mercury was added as Hg2+
either as a Hg(NO3)2 or HgCl2. The two possible Hg(II) precipitates are Hg(OH)2(s) and
HgCl2(s). Figures 3.1 and 3.2 show Hg(II) speciation if a total of 1E-5 M and 5E-4 M Hg
was added to solution and Hg(OH)2(s) was allowed to precipitate. At 1E-5 M, all of the
Hg2+ remains in solution and the dominant species between pH 4 and 10 is the uncharged
Hg(OH)2. At 5E-4 M, the main species across pH 4 and 10 remains the same, however,
the concentration is high enough for Hg(OH)2(s) precipitation. Hg spiked experiments in
this thesis were all below 1E-5 M HgT therefore no precipitation was expected. Figure 3.3
shows Hg2+ speciation for a 1E-5 M total Hg concentration in the presence of chloride
where the dominant species are uncharged HgCl2 and HgOHCl up to around pH 8. These
species dominate even more as chloride concentrations increase. Again, at the
concentration of 1E-5 M, which was above experimental concentrations, no precipitates
formed.
Table 3.3: Formation constants for Hg2+species, Log K’s for ionic strength = 0.
Equilibrium Reaction Log K HgP
2+P + OHPP
-PP = Hg(OH)P
+PP 10.6
HgP
2+P + 2OHPP
-P = Hg(OH)B2BB B 21.8
HgP
2+P + 3OHPP
-P = Hg(OH)B3PBB
-P 20.9
HgP
2+P + ClP
- P
P = HgClP
+PP P 7.2
HgP
2+P + 2ClP
-P = HgClB2BP P
P B B 14.0 HgP
2+P + 3ClP
-P = HgClP
3-PP P
P P 15.1 HgP
2+ P+ 4ClP
-P
P = HgClBPB4PB
2-P 15.4
HgP
2+P + ClP
-P + OHPP
PP
- P= HgOHCl 18.1
HgP
2+P + 2OHPP
-P = Hg(OH)B2(s)BB B 25.4
HgP
2+P + 2ClP
- P
P = HgClBB2(s)BB 14.21 P
23
pC-pH Diagram for 1E-5 M HgT, Hg(OH)2(s) allowed to precipitate
0
5
10
15
20
25
30
0 2 4 6 8 10 12 14
pH
pC
Hg2+HgOH+Hg(OH)2Hg(OH)3
Hg2+
Hg(OH)+
Hg(OH)2
Hg(OH)3-
Figure 3.1: Speciation of 1E5 M Hg2+.
pc-pH Diagram for 5E-4 M Hg2+. Hg(OH)2(s) allowed to precipitate
0
5
10
15
20
25
30
0 2 4 6 8 10 12 14
pH
pC
Hg2+HgOH+Hg(OH)2Hg(OH)3-
Hg2+
Hg(OH)+
Hg(OH)2
Hg(OH)3-
Figure 3.2: Speciation of 5E-4 M Hg2+.
24
pC-pH Diagram for 1E-5 M Hg2+ and 1E-3 M Cl-. Hg(OH)2(s) and HgCl2(s)
allowed to precipitate.
0
5
10
15
20
25
30
35
0 2 4 6 8 10 12 14
pHpC Hg2+
HgCl+HgCl2HgCl3HgCl4Hg(OH)+Hg(OH)2Hg(OH)3-HgOHCl
HgCl2 Hg(OH)2HgOHCl
Figure 3.3: Speciation of 1E-5M Hg2+ with 0.001M Cl-.
25
CHAPTER 4: RESULTS AND DISCUSSION
4.1 Introduction
Presented in this chapter are the experimental results for sediments from Guyana’s
Arakaka/Mathew’s Ridge mining region and model mineral oxide: total mercury
concentrations by cold vapor atomic absorption analysis (CVAAS), surface area analysis,
scanning electron microscopy (SEM), and electron dispersive spectroscopy (EDS/XRD).
Results from equilibrium sorption experiments are also presented.
4.2 Total Mercury Analysis
Total mercury sediment loadings were determined for all samples collected by Guyana’s
Institute of Applied Science during May 2005 for the Guyana WWF office. For total
mercury concentrations, samples were sent to a Tampa-based environmental wet
chemistry laboratory, Advanced Environmental Labs (AEL). AEL digestion methods
were based on Standard Methods 6971 for manual cold-vapor atomic adsorption analysis
and the results are summarized in Table 4.1.
Samples collected from the Arakaka area (Arakaka Creek #12, Arakaka Creek #3, and
Arakaka Creek #8) exhibited total mercury concentrations close to global and local
background concentrations of 70 ng/kg 70 and 42-77 ng/kg 2 respectively. Mercury
levels in the remaining samples were within a range of 98-300 ng/kg which are similar to
levels reported in the Brazilian Amazon mining areas (180-406 ng/kg ) 71, 72.
26
Elevated mercury levels in tropical rainforests are enhanced by temporal variations 73;
organic content 35, 74; proportion of iron containing minerals 35, rainfall 35, 75, soil
microbial activity 35, 76, and the extent of pollution. Mine waste sediment, Philip’s Mine,
contained the highest total mercury concentrations when compared to other samples
collected from the area (excluding Water Source for MWJ), which was consistent with
mine tailings or waste results obtained from Gray et al.77
Table 4.1: Total mercury concentrations in Mathew's Ridge/Arakaka area.
THg in Region 2 of Guyana
Sample ID THg
(ng/g)
Coordinates78 (DMS)
Elevation78 (ft)
Arakaka Creek #9 (Up Falls Top) 98 N07° 35.167 W060° 01.183 29 Arakaka Creek #12 (Bamboo Creek) 41 N07° 34.799 W060° 00.13
13
Arakaka Creek #13 73 N07° 34.762 W060° 01.170 91 Arakaka Creek #8 (Down Manicora) 61 N07° 34.784 W060° 00.186 145 Pakera Creek #5 200 Arakaka Creek #1 (Near River) 130 N07° 35.431 W059° 58.714 63 Pakera Creek Reservoir #14 290 N07° 29.508 W060° 08.044 21 Control Arakaka Creek #10 (Ravine Off Red Hill)
110 N07° 35.574 W059° 59.378 62 Sediment Arakaka #4 180 N07° 34.761 W060° 01.183 29 Water Source For MWJ (#1) 1200 -- -- -- Philips Tailings #1 300 -- -- -- Minab #7 200 N07° 29.956 W060° 09.238 63 Soldier Pool #6 190 N07° 29.359 W060° 11.120 54
Three of the samples with the highest concentrations were further analyzed to describe
the possible fate/transport of mercury in the aquatic environment. Limited quantities of
sediment, “Water source for MWJ”, prevented adsorption studies with this sample even
though its mercury loadings were highest amongst the sampled sediments/soils.
27
4.3 BET SEM/EDS and XRD
BET, SEM imaging coupled with EDS/EDX spectra for individual samples of Kemiron,
Pakera Creek #14, and Philips Tailings #1 were collected to determine particle
morphology, surface area, and chemical information. BET surface areas were 40 m2/g,
25.8 m2/g and 4 m2/g for Kemiron, Pakera Creek #14, and Philip’s Tailings #1,
respectively. The low surface area of the ground Philip’s Mine tailings was expected
since the material resembled an iron oxide -coated sand and sand usually has a very low
surface area. Figures 4.1-4.3 show the SEM images of these three samples. The
Kemiron surface appears porous with small (~2 μm) particle deposits on the surface. The
Pakera Creek and Kemiron samples both showed surfaces consisting of particle
agglomerations that were flaky in nature. EDS/EDX and the corresponding SEM images
in Figure 4.4 – 4.6 suggest that carbon weight percentages are 45.76%, 40.38%, and 8.24
for Philips Mine, Pakera Creek, and Kemiron solids, respectively. High carbon contents
for Philip’s Mine and Pakera Creek solids may be indicative of high organic matter
content, which was expected given that the sampling location was in a tropical rainforest.
This high organic matter content may contribute to the flaky aggregate appearance seen
in the Philip’s Mine and Pakera Creek samples. The presence of organic matter may
influence the adsorption of trace metals. Paktunc et al. 22 found high concentrations of
organic matter in the sediments of the Potaro River in Guyana, even in unmined ore next
to a mining pit. Kemiron, a commercially available iron oxide showed low C content,
which was expected. It should be noted that a carbon based tape was actually used to
secure the sample on the holder for SEM and this may contribute to some background
carbon concentrations being recorded for the Kemiron sample.
In addition, the weight percentage of mercury in the Kemiron sample was 1.76% where
as Pakera Creek and Philip’s Mine samples were 0.61% and 0.77%, respectively. This
increased weight percent determined in the Kemiron sample may be due to contamination
during the sample loading and prepping process for the SEM/EDS analysis. The sample
results for Pakera Creek (Figure 4.5) and Philip’s Mine (Figure 4.4) also show high iron
and aluminum concentrations, suggesting the presence of iron and aluminum oxides.
28
Physical characteristics and MRD PW 3060/20 XRD spectras when compared against the
online database suggest that the mineralogy of soil samples collected from Philips Mine
were predominately quartz with an iron oxide coating (Figure 4.7). On the other hand,
the Kemiron samples were composed of predominately iron hydroxide (Figure 4.8).
29
Figure 4.1: SEM image of Kemiron for particles up to to 38 μm in diameter.
Figure 4.2: SEM image of Pakera Creek for particles up to to 38 μm in diameter.
Figure 4.3: SEM image of Philip’s Mine for particles up to to 38 μm in diameter.
30
Philip s T ailings
E lem W t % A t%
C K 45 .76 56.35
O K 40 .53 37.47
A l K 4 .32 2 .37
Si K 5 .91 3 .11
S 0.01 0
B a 0 .42 0 .05
Fe K 2 .28 0.6
H g L 0 .77 0 .06
Philip s T ailings
E lem W t % A t%
C K 45 .76 56.35
O K 40 .53 37.47
A l K 4 .32 2 .37
Si K 5 .91 3 .11
S 0.01 0
B a 0 .42 0 .05
Fe K 2 .28 0.6
H g L 0 .77 0 .06
Figure 4.4: EDS spectra and chemical quantification table for Philip’s Mine tailings.
Figure 4.5: EDS spectra and chemical quantification for Pakera Creek.
31
Figure 4.6: EDS spectra and chemical quantification for Kemiron.
32
Figure 4.7: XRD spectra for Philip’s Mine tailings.
Figure 4.8: XRD spectra for Kemiron.
33
4.4 Batch Equilibrium Sorption
Figure 4.9: Sediment samples (Kemiron, Pakera Creek, and Philips Mine).
The transport and fate of mercury in the aqueous compartment is directly influenced by
sorption to particle surfaces 79. Many batch equilibrium sorption experiments have been
conducted for the sorption of mercury (II) to various mineral oxide surfaces 46, 48. Batch
equilibrium sorption studies performed in this study are summarized in Table 4.2. Based
on the speciation plots in Chapter 3, no solid precipitates should form at the
concentrations used in the batch equilibrium sorption experiments. This was confirmed
by testing the aqueous mercury concentration as a function of pH when no solid was
present. Hence, the experiments using solid samples should reflect only adsorption
mechanisms.
34
Aqueous, 1000ppb Hg Standards Curve
y = 0.0049x - 0.0054R2 = 0.9986
0
0.1
0.2
0.3
0.4
0.5
0.6
0 20 40 60 80 100
Concentration
abso
rban
ce
Figure 4.10: Typical standards curve for THg analysis using CVAAS. New standards and standards curves were generated each time the instrument was run.
A typical standard curve for total mercury concentrations remaining in solution is shown
in Figure 4.10. The calibration was linear between 5 ppb and 100 ppb with less than 2%
RSD for all readings. Figures 4.11 to 4.13 plot mercury sorption as a function of pH onto
the three solid samples when mercury was added as Hg(NO3)2. For Kemiron and Pakera
solids, mercury sorption remained high across the pH region 3-9. Cationic sorption
generally shows increased sorption with pH and though this may be true for these solid
samples, the surface loading may still be too low to see that trend. For the case of
Kemiron when mercury concentrations were increased to 1,000 ppb, close to 100% was
still sorbed. This high concentration would actually mean a surface loading of 2000
mg/kg (µg/g), which shows significant potential for Kemiron as a sorbent in remediation.
Mercury sorption on Philip’s Mine tailings had the lowest of the three solids and could be
reflective of the lower surface area (an order of magnitude lower than Kemiron).
35
The Hg surface loadings on the Philip’s Mine tailings varied from 120 to 190 mg/kg
(µg/g) which was significantly higher than the results obtained from the field. The high
capacity of these solids to sorb mercury indicates their potential as sinks for mercury in
the environment.
Table 4.2: Summary of batch equilibrium sorption studies.
Solid
Solid
Concentration
(g/L)
Hg THg
(ppb)
THg
(M) Electrolyte
Ionic
Strength
Amount
sorbed/
amount of
sediment
at pH ≈ 7*
None -- HgCl2 1000
5E-6 NaNO3 0.1 --
None -- Hg(NO3)2 1000
5E-6 NaNO3 0.1 --
Kemiron 0.5 HgCl2 1000
5E-6 NaNO3 0.1 6530.61
Kemiron 0.5 Hg(NO3)2 1000
5E-6 NaNO3 0.1 9843.58
Kemiron 0.5 Hg(NO3)2 100
5E-7 NaNO3 0.1 990.39
Pakera
Creek 0.5 HgCl2 1000
5E-6 NaNO3 0.1 9671.18
Pakera
Creek 0.5 Hg(NO3)2 100
5E-7 NaNO3 0.1 922.97
Philip’s
Mine 0.5 HgCl2 1000
5E-6 NaNO3 0.1 8242.31
Philip’s
Mine 0.5 Hg(NO3)2 100
5E-7 NaNO3 0.1 995.66
*Calculations are based on data results for ≈pH 7 located in Appendix A.
36
Figure 4.11: Hg sorption to 0.5 g/L Kemiron.
Figure 4.12: Hg sorption to 0.5 g/L Pakera Creek sediment.
37
Figure 4.13: Hg sorption to 0.5 g/L Philip’s Mine tailings.
Since speciation of mercury changes in the presence of chloride ions, batch sorption
equilibrium using sodium nitrate as a background electrolyte and mercuric chloride as the
stock mercury concentration are outlined in Table 4.2.
Samples prepared by the addition of mercuric chloride are shown in Figure 4.14. In the
Kemiron samples depicted in Figure 4.15, sorption of mercury added as mercuric
chloride is lower when compared to Kemiron samples prepared from mercuric nitrate.
38
Figure 4.14: Hg sorption of 0.5 g/L of soil for 1,000 ppb Hg (from HgCl2).
Hg sorption to 0.1g/200mL Kemiron For 1000ppb Hg, 0.1N NaNO3
0%
20%
40%
60%
80%
100%
2 3 4 5 6 7 8 9 10 11
pH
% s
orbe
d
Hg added as HgCl2 Hg added as Hg(NO3)2
Figure 4.15: Hg Sorption of 0.5 g/L of soil for 1,000 ppb Hg (from HgCl2 and Hg(NO3)2).
39
Sorption characteristics for natural soil samples collected from Guyana which were
prepared to a total mercury concentration of 1,000 ppb using HgCl2 stock solution
indicate that in alkaline conditions (pH 8-10) sorption at the surface-mineral interface is
relatively higher when compared to highly acidic conditions (pH 3-5) (Figure 4.14).
However, when above pH 5 a distinct difference in sorption is observed for the
commercially available iron-oxide soil prepared with HgCl2 when compared to natural
samples. It appears that sorption begins to decrease above pH 5 in the Kemiron samples.
The behavior of mercury (II) at the solid/water interface by batch experiments has been
studied widely 42, 46. Kim et al. 42 examined the effects of chloride and sulfate, common
complexing ligands, to mineral sorbents of goethite (alpha-FeOOH), gamma-alumina
(gamma-Al2O3), and bayerite (beta-Al(OH)3) by extended x-ray adsorption fine structure
(EXAFS) spectroscopy. By measuring the uptake of Hg (II) at pH 6 with an initial
mercury concentration of 0.5 mM, Kim et al. 42 illustrated that the presence of chloride
with concentrations of 10-5 to 10-2 M resulted in the reduction of mercury (II) sorption.
Bonnissel-Gissinger et al. 46 modeled the sorption of Hg (II) onto amorphous silica
(Aerosil 200) and α-FeOOH, goethite (Bayferrox 910), using various 68 pH conditions.
The results by Bonnissel-Gissinger et al. 46 for the mineral sorbent, goethite, were
consistent with data results from Kim et al 42 which suggests that the presence of chloride
limited the sorption of mercury to oxide surfaces due to the formation of stable metal–
ligand aqueous complexes that do not absorb. However, Bonnissel-Gissinger et al.46
further suggested that the structures of the oxides (Aerosil 200) and iron-oxides did not
influence the sorptive capabilities of the samples. Wang et al.68 examined the influence
of chloride/mercury molar ratio and pH on the adsorption of mercury by poorly
crystalline oxides of Al, Fe, Mn, and Si. They reported that as the molar ratio of Cl/Hg
increased, sorption decreased due to the formation of aqueous Hg-Cl complexes.
The results from Figure 4.14 combined with the spectroscopic results presented in
Figures 4.4 and 4.5, revealed a high organic content in the natural samples of Philip’s
Mine tailings and Pakera Creek sediment: 45.76% and 40.38% by weight, respectively..
The organic portion of the natural samples likely provided stronger complexing sites
40
when compared to Kemiron (8.24% by weight). According to the investigation of
mercury distribution in waters of the coastal lagoons of Rio de Janeiro, Brazil, Lacerda
and Goncalves80 found that most dissolved mercury was strongly bonded to refractory
organic colloids. The Kemiron has the largest surface area of the three solids tested
which from a strictly sorption perspective would be expected to have the highest sorption
capacity. The type of mineral oxide or the presence of other complexing ligands in the
system resulted in the aqueous chloride complexes out-competing the Kemiron for
mercury more than the real sediment samples. This was especially true above pH 5. The
Philip’s Mine samples, which had a very low surface area also showed a strong binding
capacity for mercury. These tailings also show significant amounts of carbon and it is
reasonable to assume that that carbon is in the form of natural organic matter since no
carbonate minerals were identified by XRD. For the experiment with mercuric chloride,
the natural organic matter appeared to play a major role in competing with aqueous
mercury chloride complexes in the real sediment samples.
Hence, in this tropical rainforest region, natural organic matter (NOM) may have play a
significant role in mercury distributions. Further studies are needed to understand the
effect NOM has on mercury speciation/transformation reactions like abiotic photolysis.
A 24-hour equilibration time was used for all experiments. Kinetic tests were not
performed to validate this choice of equilibration period. Based on previous literature it
is possible that longer equilibration times were needed for batch reactor experiments.
41
CHAPTER 5: SUMMARY, CONCLUSION, & RECOMMENDATIONS FOR FUTURE
WORK
5.1 Introduction
The bioavailability, speciation, fate and transport of mercury in the environment can be
influenced by several natural and anthropogenic activities like soil degassing, volcanic
eruptions, mining, and industrial waste discharge. This section provides a summary of the
experimental results, conclusions, and recommendations for future work.
5.2 Summary of Results and Conclusions
The main objectives for studies on the samples collected from Guyana’s Mathews
Ridge/Arakaka area were to provide the following:
• Determine total mercury concentrations within the soil compartment
o Total mercury concentrations of the collected soil/sediment samples were
within the range of background mercury loadings reported in the
Amazonian mining districts (180-406 ng/kg 2, 22). One sample, MWJ,
reported mercury loadings of 1200 ng/kg. The samples were ground and
mixed prior to analysis and hence the results represent average loadings.
• Physical/Chemical characterization of soil samples
o Philip’s Mine tailings and Pakera Creek sediment as well as a
commercially available iron oxide, Kemiron, were subjected to BET
surface area, XRD, SEM/EDS analysis. The Philips Tailings had the
lowest surface area (4 m2/g) whilst Kemiron had the highest (40 m2/g).
SEM/EDS showed that the Philip’s Mine and Pakera Creek samples had
42
high carbon content likely due to the presence of natural organic matter;
however results may be inaccurate due to possible cross contamination of
sampling due to loading procedures. XRD identified goethite as the main
iron oxide phase present in Kemiron and SEM/EDS suggested that surface
impurities may include mercury. The ground (less than 38 μm) Kemiron
sample showed a porous surface with crystalline particle deposits.
• Determine the potential for mercury sorption by soil samples based on batch
reactor studies
o Simultaneous acidification of ground and surface waters can lead to an
increase in the mobility of mercury bound to soils and sediments 48.
Similarly, soils and sediments can act as potential sinks for mercury in the
environment. Batch adsorption studies of mercury on the Philip’s Mine
tailings, Pakera Creek sediments and Kemiron showed significant sorption
between pH 3 and 9 for conditions of 1 g/L solid and 100-1000 ppb Hg
added as Hg(NO3)2. The Philip’s Mine tailings sample showed the lowest
sorption and this was expected based on its low surface area compared
with Kemiron or the Pakera Creek sample. The Pakera Creek and
Kemiron samples showed similar behavior with high sorption across all
pH ranges and surface loadings around 200 mg/kg for the 100 ppb Hg
experiments and 2000 mg/kg for experiments with 1000 ppb Hg.
o Adsorption behavior of Hg2+ onto commercially available Kemiron, an
iron-oxide surface, exhibited decreased sorption patterns when mercuric
chloride was added to the system compared to the addition of mercuric
nitrate.
43
5.3 Recommendations for Future Work
• Further identification of binding mechanisms between mercury and sediment
samples is needed. This will include both sequential leaching techniques and
further spectroscopic analysis and modeling.
• Study of the role of organic matter in mercury mobility. This will include
quantification of organic matter content of soil/sediment samples as well as
mercury partitioning to these phases.
• Kinetic tests should be conducted to predict the possible fate and transport of
mercury (II) in soils.
• Future sampling in Guyana should be accomplished, especially in areas with
higher mercury concentrations, and better correlations made with aqueous
environmental parameters (pH, turbidity, alkalinity, TDS). Partnerships with the
local community and non-governmental organizations should be sought to not
only ensure continued access to the sampling sites and collected data, but also for
the sustained development of solutions to the potential pollution problems.
• The use of Kemiron as a sorbent for mercury under various geochemical
conditions including the presence of organic matter and other competing ions
should be further explored. This could lead to its further use as a remediation
procedure.
This research project examined the sorptive capabilities of sample Guyanese soils located
close to small-to-medium scale mining operations in the Arakaka and Mathew’s Ridge
region. These soils can act as potential sinks or sources for mercury and an
understanding of geochemical conditions that affect the fate of mercury can inform
solutions for reduced environmental impacts of mercury contamination. The motivation
for the work lies in understanding and reducing the environmental impact of mercury
used in the mining sector. This region is populated by scattered communities with
limited access to health care, analytical labs or centralized or coordinated drinking water
treatment and distribution systems. As local organizations like the Guyana WWF attempt
to assess the extent of mercury contamination and human exposure, a sustained
44
relationship with studied communities is definitely needed. More importantly,
multidisciplinary teams of researchers should be encouraged to further this work and
provide opportunities that not only further scientific research, but provides both
immediate and long term solutions to the local community. In a politically fragile
environment like Guyana, ways to form partnerships with local communities and non
governmental organizations are encouraged.
45
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75. Lacerda, L. D.; Paraquetti, H. H. M.; Rezende, C. E.; Silva, L. F. F.; Silva, E. V.; Marins, R. V.; Ribeiro, M. G., Mercury Concentrations in Bulk Atmospheric Deposition over the Coast of Rio De Janeiro, Southeast, Brazil. Journal Of The Brazilian Chemical Society 2002, 13, (2), 165-169.
76. Guimaraes, J. R. D.; Meili, M.; Malm, O.; Brito, E. M. D., Hg Methylation in Sediments and Floating Meadows of a Tropical Lake in the Pantanal Floodplain, Brazil. Science Of The Total Environment 1998, 213, (1-3), 165-175.
77. Gray, J. E.; Hines, M. E.; Higueras, P. L.; Adatto, I.; Lasorsa, B., Mercury Speciation and Microbial Transformations in Mine Wastes, Stream Sediments, and Surface Waters at the Almaden Mining District, Spain. Environ. Sci. Technolo. 2004, 4285-4292.
78. Bera, S. Wwf Iast Mercury Impact Assessment Project-Region 1: Arakaka, Mathew's Ridge and Port Kaituma; IAST: Georgetown, Guyana, June 10, 2005, 2005; pp 1-5.
79. Kim, C. S.; Rytuba, J. J.; Brown, G. E., Geological and Anthropogenic Factors Influencing Mercury Speciation in Mine Wastes: An Exafs Spectroscopy Study. Applied Geochemistry 2004, 19, (3), 379-393.
80. Lacerda, G. O. G. L. D., Mercury Distribution and Speciation in Waters of the Coastal Lagoons of Rio De Janerio, Se Brazil. Marine Chemistry 2001, (76), 47-58.
53
APPENDICES
54
Appendix A: Abridged Experimental Data Results
Tabular report of the equilibrium sorption experiments discussed in Chapter 4. Data
results have been grouped according to sample name then by the mercury stock solution
(i.e. HgCl2 or Hg(NO3)2).
Table A.1: 100 ppb Hg (Hg(NO3)2) sorption on 0.1 g Pakera Creek sediment (1.1).
Experiment 1.1:
100 ppb Hg (Hg(NO3)2) Sorption on 0.1 g Pakera Creek
Sediment
Background electrolyte: 0.1 N sodium nitrate
pH
THg (ppb) % Hg Sorbed
3.68 5.11 95%
3.97 4.90 95%
5.26 2.11 98%
5.41 4.45 96%
5.63 3.13 97%
5.69 1.57 98%
5.84 0.63 99%
5.86 2.95 97%
6.01 4.72 95%
6.90 7.70 92%
7.31 4.11 96%
55
Appendix A: (Continued)
Table A.2: 100 ppb Hg (Hg(NO3)2) sorption on 0.1 g Pakera Creek sediment (1.2).
Experiment 1.2:
100 ppb Hg Sorption on 0.1 g Pakera Creek Sediment
Background electrolyte: 0.1 N sodium nitrate
pH
THg (ppb) % Hg Sorbed
3.10 5.47 90%
5.27 5.04 90%
6.02 5.51 89%
6.49 5.04 90%
6.70 6.66 88%
6.75 5.64 89%
6.91 5.57 89%
7.16 10.51 84%
7.40 1.06 84%
7.80 5.43 90%
9.34 5.28 90%
56
Appendix A: (Continued)
Table A.3: 100 ppb Hg (Hg(NO3)2) sorption on 0.1 g Philip’s Mine tailings (2.1).
Experiment 2.1:
100 ppb Hg (Hg(NO3)2) Sorption on 0.1 g Philip’s
Mine tailings
Background electrolyte: 0.1 N sodium nitrate
pH THg (ppb) % Hg Sorbed
3.10 7.83 92%
3.39 5.47 95%
3.54 6.33 94%
4.10 31.07 69%
4.52 34.95 65%
4.85 32.95 67%
5.51 9.47 91%
5.63 92.76 7%
5.79 12.90 87%
5.87 7.60 92%
7.38 4.97 95%
57
Appendix A: (Continued)
Table A.4: 100 ppb Hg (Hg(NO3)2) sorption on 0.1 g Philip’s Mine tailings (2.2).
Experiment 2.2:
100 ppb Hg (Hg(NO3)2) Sorption on 0.1 g Philip’s
Mine tailings
Background electrolyte: 0.1 N sodium nitrate
pH THg (ppb) % Hg Sorbed
3.57 0.72 89%
3.96 18.06 71%
6.34 7.55 76%
6.47 5.87 83%
7.30 0.75 71%
9.56 0.43 88%
58
Appendix A: (Continued)
Table A.5: 100 ppb Hg (Hg(NO3)2) sorption on 0.1 g Kemiron (3.1).
Experiment 3.1:
100 ppb Hg (Hg(NO3)2) Sorption on 0.1 g Kemiron
Background electrolyte: 0.1 N sodium nitrate
pH THg (ppb) % Hg Sorbed
4.37 0.18 100%
4.71 0.10 100%
5.08 0.06 100%
5.39 0.10 100%
5.98 0.35 100%
6.58 0.35 100%
7.29 0.27 100%
7.44 0.30 100%
8.21 0.13 100%
59
Appendix A: (Continued)
Table A.6: 100 ppb Hg (Hg(NO3)2) sorption on 0.1 g Kemiron (3.2).
Experiment 3.2:
100 ppb Hg (Hg(NO3)2) Sorption on 0.1 g Kemiron
Background electrolyte: 0.1 N sodium nitrate
pH THg (ppb) % Hg Sorbed
4.24 0.09 96%
5.49 0.11 96%
6.24 0.41 96%
6.93 0.19 96%
7.74 0.41 96%
9.03 0.39 96%
Table A.7: 100 ppb Hg (Hg(NO3)2) sorption on 0.1 g Kemiron (3.3).
Experiment 3.3:
100 ppb Hg (Hg(NO3)2) Sorption on 0.1 g Kemiron
Background electrolyte: 0.1 N sodium nitrate
pH THg (ppb) % Hg Sorbed
4.07 0.13 96%
5.07 1.76 96%
6.26 0.27 96%
7.38 0.40 96%
8.03 1.67 95%
60
Appendix A: (Continued)
Chapter 4.4: Equilibrium sorption experiments. Kemiron; Hg Spike from mercuric
nitrate with varied total mercury concentrations of 200 and 1,000 ppb.
Table A.8: 1,000 ppb Hg (Hg(NO3)2) sorption on 0.1 g Kemiron (4.1).
Experiment 4.1:
1000 ppb Hg (Hg(NO3)2)Sorption on 0.1 g Kemiron
Background electrolyte: 0.1 N sodium nitrate
pH THg (ppb) % Hg Sorbed
3.07 8.85 99%
3.66 10.26 99%
3.92 10.64 99%
4.53 11.68 99%
4.97 13.66 99%
5.99 14.70 99%
6.45 15.64 98%
7.95 16.77 98%
9.62 17.91 98%
9.92 18.38 98%
61
Appendix A: (Continued)
Chapter 4.4: Equilibrium sorption experiments for all samples (Pakera Creek, Philips
Tailings, and Kemiron); Hg spike from mercuric chloride with varied total mercury
concentrations of 1,000ppb.
Table A.9: 1,000 ppb Hg (HgCl2) sorption on 0.1 g Pakera Creek (5.1).
Experiment 5.1:
1,000 ppb Hg Sorption on 0.1 g Pakera Creek Background electrolyte: 0.1 N sodium nitrate
pH THg (ppb) % Hg Sorbed
2.86 430.32 57% 3.4 390.38 61%
4.84 294.61 71% 6.85 32.88 97% 8.74 37.21 96% 5.57 80.96 92% 4.43 307.59 69%
Table A.10: 1,000 ppb Hg (HgCl2) sorption on 0.1 g Philip’s Mine (5.2).
Experiment 5.2:
1,000 ppb Hg Sorption on 0.1 g Philip’s Mine tailings Background electrolyte: 0.1 N sodium nitrate
pH THg (ppb) % Hg Sorbed
2.68 256.92 74% 4.6 241.06 76%
6.23 175.77 82% 5.36 233.27 77% 8.67 55.10 94% 8.88 55.38 94% 9.04 44.52 96%
62
Appendix A: (Continued)
Chapter 4.4: Equilibrium sorption experiments for all samples (Pakera Creek, Philips
Tailings, and Kemiron); Hg spike from mercuric chloride with varied total mercury
concentrations of 1,000 ppb.
Table A.11: 1,000 ppb Hg (HgCl2) sorption on 0.1 g Kemiron (5.3).
Experiment 5.3:
1000 ppb Hg Sorption on 0.1 g Kemiron Background electrolyte: 0.1 N sodium nitrate
pH THg (ppb) % Hg Sorbed
2.84 356.36 64% 3.28 383.67 62% 4.44 380.88 62% 4.94 367.42 63% 5.46 302.80 70% 6.35 346.94 65% 8.51 462.04 54%
63
Appendix A: (Continued)
Chapter 4.3: EDS Quantification Results
All electron dispersion graphic signals and quantification results were taken at 25kV with
a tilt of 30 and take-off of 36.31 at total counts of 100.0 seconds.
Table A.12: EDS quantification Table A.13: EDS quantification (Arakaka Creek) (Kemiron)
Arakaka Creek Kemiron <38μm
Elem Wt % At% K-Ratio Elem Wt % At% K-Ratio
C K 23.41 33.41 0.0398 C 8.24 16.29 0.0208
O K 44.23 47.39 0.1115 O 41.64 61.72 0.1699
F K 1.02 0.92 0.0015 Mg 3.44 3.36 0.0095
Al K 1.46 0.93 0.0092 Ca 0.44 0.26 0.0042
Si K 27.65 16.88 0.2069 Fe 42.12 17.9 0.3893
Fe K 1.29 0.4 0.0113 Hg 1.76 0.21 0.0127
HgL 0.95 0.08 0.0066 Pb 2.39 0.27 0.0169
Table A.14: EDS quantification (Philip’s Mine)
Philips Tailings
Elem Wt % At% K-Ratio
C K 44.79 55.87 1.0192
O K 39.14 36.66 1.0038
Al K 4.34 2.41 0.9382
Si K 7.6 4.05 0.9662
K K 0.15 0.06 0.912
Ca K 0.02 0.01 0.9357
Ti K 0.34 0.11 0.8588
Fe K 2.88 0.77 0.8585
Hg L 0.74 0.05 0.6569
64
Appendix A: (Continued)
Chapter 4.3: EDS Quantification Results
All electron dispersion graphic signals and quantification results were taken at 25kV with
a tilt of 30 and take-off of 36.31 at total counts of 100.0 seconds.
Table A.15: EDS quantification Table A.16: EDS quantification (Pakera Creek) (Pakera Creek (2))
Pakera Creek Pakera Creek
Elem Wt % At% K-Ratio Elem Wt % At% K-Ratio
C 22.2 32.48 0.0438 C 40.38 53.03 0.1123
O 45.93 50.44 0.1256 O 38 37.47 0.0843
Al 7.68 5.00 0.044 Fe 8.42 2.38 0.224
Si 15.25 9.54 0.0964 Al 4.58 2.68 0.0263
S 0.06 0.03 0.0004 Si 7.51 4.22 0.05
Cl 0.11 0.05 0.0008 K 0.22 0.09 0.002
K 0.53 0.24 0.0045 Ti 0.22 0.07 0.002
Ba 0.94 0.12 0.0079 Mn 0.05 0.02 0.0005
Mn 1.07 0.34 0.0093 Hg 0.61 0.05 0.0042
Fe 5.31 1.67 0.0468
Hg 0.93 0.08 0.0065
65
Recommended