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Review
Mercury in petroleum
S. Mark Wilhelm
a
a,)
, Nicolas Bloom
Mercury Technology Serices, 23014 Lutheran Church Rd., Tomball, TX 77375, USA
b
Frontier Geosciences, Seattle, WA, USA
Received 30 September 1999; accepted 30 September 1999
Abstract
The understanding of the chemistry of geologic mercury has evolved due to technical advances
that allow differentiation of the various chemical forms of mercury in hydrocarbon matrices.
Newly developed techniques can measure the concentration of mercury and mercury compounds
in some hydrocarbon matrices to better than 1 part in 10 10. Accurate determinations of total
mercury and speciation of mercury compounds depend on sophisticated sampling techniques and
rigorous analytical procedures. The mercury species that are present in crude oil and gas
condensates include several that are seldom accounted for in routine analytical methodology.
Although only limited amounts of data are presently available, it appears that the distribution of
mercury compounds in petroleum samples varies widely. The amounts and relative distribution of
mercury compounds in liquid hydrocarbons depend on the sample source and history and include
classes of compounds that have specific negative effects on people, equipment and catalysts.
Crude oil and unprocessed gas condensates contain significant amounts of suspended mercury
compounds, mostly mercuric sulfide. The dominant dissolved species in petroleum are elemental
mercury and ionic halides. Ionic mercury compounds have been found in significant proportions in
liquids but it is not known if they are abundant naturally or if they exist due to post-collection
conversion of other mercury species. Detection and quantification of dialkylmercury in liquid
hydrocarbons have been accomplished analytically but only limited data are available concerning
its prevalence in petroleum and processed fuels. The recent understanding of the toxicology of
dialkylmercury identifies this class of compounds as a potential health hazard to those exposed to
gas condensate and oil, but hard evidence of exact concentrations is needed to support the
hypothesis of possible risk. Mercury removal systems that employ sorbents to capture mercury in
feeds to gas and liquid hydrocarbon processes do not work effectively on all chemical forms of
mercury. Suspended colloidal. forms, such as mercuric sulfide, evade capture by sorbent beds
and organic mercury compounds are captured to varying degrees depending upon sorbent
chemistry. Understanding the reaction of chemisorbents with each of the various species that are
0378-3820r00r$ - see front matter q 2000 Elsevier Science B.V. All rights reserved.
PII: S 0 3 7 8 - 3 8 2 0 9 9 . 0 0 0 6 8 - 5
present in feeds is essential to the design of mercury removal systems. Mercury is universally
detrimental to petroleum processing systems. In gas processing, mercury damages equipment and
fouls cryogenic heat exchangers. In chemical manufacturing and refining, mercury poisons
catalysts and contaminates waste water, thus impacting regulatory compliance. Contamination of
primary gas treatment systems amine and glycol. and accumulation of toxic sludge deposits in
separators generate waste streams that are difficult to dispose of. Maintenance workers in the
petroleum industry can be at risk due to inhalation of mercury vapor and dermal absorption of
organic mercury compounds unless proper precautions are implemented. q 2000 Elsevier Science
B.V. All rights reserved.
Keywords: Mercury; Petroleum; Hydrocarbon
1. Introduction
In the recently submitted US EPA Mercury Report to Congress w1x, combusted
hydrocarbons are identified as major anthropogenic sources of mercury emissions to the
atmosphere in the US. It is estimated that approximately 11 tons 10 Mg. of mercury are
discharged to the atmosphere annually from boilers that burn oil. The 11 tons are
approximately 7% of the US domestic total 158 tons. from all sources. Water
discharges from refineries and petrochemical plants have been identified as sources of
aquatic mercury contamination.
The mercury in combusted fuels originates from petroleum and coal. The concentration of mercury in crude oil and natural gas is highly dependent on geologic location and
varies between approximately 0.01 ppb and 10 ppm wt... Eventually, the mercury in
combusted hydrocarbons contributes to the atmospheric mercury cycle where it distributes, by recently identified mechanisms and pathways, to marine and lacustrine
ecosystems w2x. The causes and consequences of mercury deposition to marine environments have been reviewed in Volume 4 of the Mercury Report to Congress.
The contribution of mercury in petroleum-based fuels to the global mercury cycle is
difficult to estimate because of the lack of data on concentrations of mercury compounds
in common fuels and the lack of mechanistic information on the fate of mercury
compounds in liquid fuel combustion. The mercury compounds in exhaust gas from
burning petroleum fuels are likely to be different than those originating from coal
combustion. In spite of the fact that the total amount of mercury compounds in
petroleum-based fuels is thought to be low, the sheer volume of liquid fuel combustion
requires that the concentrations of mercury compounds in petroleum be accurately
assessed.
In addition to the contribution of geologic mercury to atmospheric pollution, mercury
in oil and gas has a direct negative impact on petroleum processes. The consequences of
mercury in feeds on processing systems include equipment degradation, toxic waste
generation, increased risk to the health and safety of workers and poisoning of catalysts.
Mercury in plant feeds often requires process modifications to avoid the negative
consequences and to comply with product specifications. Speciation of mercury compounds in liquid hydrocarbons is necessary to understand the mechanisms of the
interaction of the various species with equipment, catalysts, mercury removal systems
and personnel.
Recent technical advances have improved our understanding of the chemistry of
mercury in petroleum systems. Analytical methods are now capable of measuring
mercury concentrations at very low levels and to differentiate quantitatively many of the
chemical forms of mercury. The newly acquired understanding assists in identifying
exposure risks, selection of mercury removal systems and waste processing for disposal.
2. Background
Elemental mercury and several mercury compounds occur naturally in geologic
hydrocarbons. At ambient temperature, elemental mercury Hg 0 . is soluble in liquid
aliphatic hydrocarbons to a few 13. ppm see Fig. 1., which is several times greater
than its 0.05-ppm solubility in water. Elemental mercury is highly adsorptive and
adsorbs on metallic surfaces and on solid materials sand. suspended in liquids. Hg 0
reacts with iron oxide corrosion products on pipe and equipment walls. The solubility of
Hg 0 in produced hydrocarbons depends strongly on temperature, hence, when saturated
liquids are cooled, Hg 0 can precipitate in equipment.
Table 1
Boiling points of volatile mercury compounds
Boiling point 8C.
Hg compound
0
Hg
CH 3 . 2 Hg
C 2 H 5 . 2 Hg
C 3 H 7 . 2 Hg
C 4 H 9 . 2 Hg
357
96
170
190
206
Table 2
Solubility of some mercury compounds in hexane
Species
0
Hg
HgCl 2
CH 3 HgCl
CH 3 . 2 Hg
Solubility ppb.
Temperature 8C.
1,200
11,500
)1,000,000
`
27.5
27.5
20.0
separations. Also included in this category are mercury compounds that are not
dissolved but rather adsorbed on inert particles such as formation fines.
The various chemical forms of mercury exhibit significantly different chemical and
physical behavior. Each chemical form requires analytical methodology that is specific
to its particular characteristics. Analytical procedures are formulated to take advantage
of the differences in species adsorptive character, solubility and volatility. Boiling points
of organic compounds Table 1. assist prediction of the distribution of compounds in
distillations of crude oil. The solubilities of some mercury compounds in hexane are
compiled in Table 2 and are useful to predict the distribution of compounds in phase
separations. The solubility of elemental mercury in alkanes as a function of temperature
is shown in Fig. 1 w3x.
3. Analytical methods
Analytical methods for mercury and mercury compounds in hydrocarbon matrices are
differentiated by collection sampling., species conversionrseparation digestion, extraction, filtration, vaporization. and detection methods. The methods used to determine
total mercury in liquid and gaseous hydrocarbons are reasonably well-established and
accurate. The methods to quantitatively speciate mercury compounds in liquid hydrocarbons are more recent and less verified. The speciation methodologies now practiced are
categorized as either operational or species-specific.
3.1. Sampling
Sampling of hydrocarbons containing mercury is difficult to accomplish because of
partitioning of mercury compounds among phases, species interconversion in some
sample containers, loss of non-polar compounds in plastic containers and due to
adsorption of mercury on sample container surfaces. In samples derived from hot
andror pressurized streams, the volatile mercury compounds Hg 0 and HgCH 3 . 2 .
partition between the vapor and liquid phases in sample containers. Analysis of both the
liquid and gas phases and a mass balance is therefore required if the concentration of
mercury in the produced phase is required.
The amounts of Hg 0 and RHgR that partition to water is usually a small percentage
of the total mercury concentration in coexisting phases because of their low solubilities
in water. Ionic mercury compounds, however, if present, will partition to the water
phase but the hydrocarbonrwater partition ratios depend on pH, salinity, temperature
and other factors. Acidic water can encourage formation of a particle rich layer at the
waterroil interface that can be very high in mercury concentration. Sampling and
analysis protocols should be designed to take these factors into account.
The adsorption of mercury on surfaces can result in considerable uncertainty because
the time to equilibrate plumbing is often unknown. Mercury concentrations in metal
containers used for pressurized liquid samples often exhibit lower than actual results due
to adsorption or reaction with corrosion products on container walls. The material of
digestion bombs. Extractive methods BrCl. are preferred for light hydrocarbon liquids
w7x.
Digestates and extracts are treated with stannous chloride or sodium borohydride to
generate Hg 0 and then sparged Ar.. The sparge gas is either sent directly to a detector
or collected on a trap amalgamation. and then thermally evolved into an inert gas
stream for detection. The amalgamation step concentrates the sample and eliminates
interference from hydrocarbons.
The most common forms of detection are cold vapor atomic absorbance w8x CVAA.
and cold vapor atomic fluorescence CVAF.. CVAF is a very sensitive method w6x with
reported absolute detection limits 100 to 700 pg. The low detection limit allows accurate
quantitation of very small samples and dramatically reduces matrix effects common to
other methods by allowing extreme dilution prior to analysis.
Other types of total mercury analysis methods include inductively coupled plasma
ICP. or microwave induced plasma MIP. followed by mass spectrometry MS. w9x or
atomic emission spectrometry AES. w10x detection. The ICPrMIP techniques avoid
digestion of the sample, hence, minimizing some of the potential errors that can occur in
multi-step wet chemical processing of liquid samples. Neutron activation analysis
NAA. methods, which also avoid wet processing of samples, also have been used to
examine crude oils w11x. NAA, ICPrMIP and MSrAES all report detection limits less
than 0.1 ngrg.
3.4. Speciation of mercury compounds
Operationally defined speciation w12,13x of liquid samples involves multiple and
sequential analyses for the various forms and a mass balance exercise.
Total Hg s Hg 0 q RHgRq HgK . q HgCl 2 q RHgCl. q suspended Hg.
1.
Total mercury concentration typically is determined by oxidative extraction. Suspended mercury is quantitatively determined by measuring total mercury of an agitated
sample followed by measuring total mercury of a filtered portion of the agitated sample.
Ionic and monoalkyl forms HgCl 2 q RHgCl. are determined by non-oxidative extraction of filtered samples using dilute acids. Hg 0 is determined by sparging and collecting
the volatile component on a trap. The sum of the concentrations of dialkylmercury and
complexed mercury often is estimated from the discrepancy in the mass balance.
Chromatographic techniques have been applied successfully to hydrocarbon liquids
and are capable to separate the various mercury species. Both gas chromatography GC.
and high-performance liquid chromatography HPLC. techniques have been used successfully.
Schickling and Broekaert w14x used HPLC, matrix destruction dichromate., borohydride reduction and CVAA to examine gas condensates. Detection limits 3 s . of
approximately 10 ng were achieved for RHgR R s phenyl., HgCl 2 and RHgCl.
Important in this work were observations of the reaction of ionic and organic mercury.
Chromatographic separation of standard mixtures of mercuric chloride and diphenylmercury produced only a peak confirmed to be monophenylmercury chloride.
RHgRq HgCl 2
2RHgCl.
2.
Whether reactions of ionic and other organic mercury compounds occur was not
examined and remains uncertain.
Snell et al. w15x used GC, post-column combustion, amalgamation PtrAu. and
MIPAES. MIPAES achieved a detection limits 3 s . between 0.25 and 5 ngrml for
the various species. Separation of organic, inorganic and monomethylmercury species
was accomplished using GC, following derivatization using Grignard reagent butylmagnesium chloride.:
CH 3 HgCl q C 4 H 9 MgCl
HgCl 2 q 2C 4 H 9 MgCl
CH 3 HgC 4 H 9 q MgCl 2
3.
C 4 H 9 HgC 4 H 9 q 2MgCl 2 .
4.
Zettlitzer et al. w16x used HPLC, post-column oxidation UV-PCO. and CVAA to
examine monoalkylmercury and GCMS to examine dialkylmercury in German condensates. The speciation scheme included operational steps for Hg 0 and HgCl 2 . The
detection limit for the GCMS procedure was greater than 1 ppm and thus, did not
allow quantitative determination of dialkylmercury.
Tao et al. w17x used GCICPMS to examine a variety of condensates and naphthas.
The procedures developed by Tao were rigorously verified as to recovery and sensitivity
using spikes, replicates and blanks. Tao optimized injection procedures for the GC and
verified recoveries close to 100% for all of the mercury species examined. Absolute
detection limits were orders of magnitude better than previously reported fg..
C5 q fraction that is a product from a gas separation plant. Naphthas typically originate
from the primary distillation of oil in the range of 508C to 1508C see Fig. 3.. The
distribution of hydrocarbon compounds in both condensates and naphthas are similar
and mostly in the range C4 to C10. Processed condensate and naphthas typically do not
contain suspended mercury compounds.
Published Hg concentrations in condensate, naphthas and crude oil often do not fully
disclose sampling procedures or analytical processing steps filtration, centrifugation,
exposure to air.. For these reasons, some data are suspect in that the total mercury
concentrations reported could include a contribution from suspended forms or the
distribution of compounds could reflect species conversion. Aerobic processing of
samples is suspected to promote oxidation of Hg 0 to ionic forms and thus to alter the
distribution of species.
The total Hg concentration reported in hydrocarbons varies widely. Some condensates and crude oils are close to saturation with Hg 0 at concentrations of 14 ppm as
determined by sparging of fresh, filtered samples. Adding suspended, ionic and organic
forms, total mercury concentrations in crude oil over 5 ppm are known. Gas condensates
in SE Asia have dissolved total Hg concentrations in the 10800 ppb range. Most crude
oils in the US have relatively low mercury concentrations.
Musa et al. w11x reported total mercury in Libyan crude oils to be in the range of 0.1
to 12 ppb. Bloom w13x found total Hg in unfiltered crude oils ranging between sub-ppb
levels to over saturation see Table 3.. The mean for crude oil 1.5 ppm, N s 76. likely
is skewed high due to samples with some suspended mercury. The mean of the lower 38
samples was close to 1 ppb. Data for crude oils are compiled in Table 3 and Fig. 4.
10
Table 3
Total Hg in liquids w13x
Oil type
76
39
37
18
10
8
14
32
10
wHgx ngrg.
Mean
SD
1505
3009
1.20
3964
7113
20.4
1.32
0.67
0.27
3278
4140
1.49
11,665
15,240
19.7
2.81
0.96
0.32
11
were filtered prior to analysis and thus, may have contained some suspended compounds. These concentrations are in the very high end of the range of total Hg
concentration in condensate. Taos data for total mercury in condensates are included in
Fig. 5 and range between 10 and 200 ugrl. Note: data in the figures have been
converted to grg for uniformity..
The presently published data for total Hg in naphthas Fig. 6. are similar to
condensates and range approximately between 5 and 200 ppb. High concentrations have
not been reported in the limited published data. Naphthas originating from distillations
would be expected to have lower concentrations than the raw produced liquids from
which they originate.
Only limited data are available that allow examination of the distribution of concentrations of mercury compounds in hydrocarbon liquids. Of interest are the natural
abundance of mercury compounds, the relative distribution of compounds in liquid
samples, the partitioning of compounds in separations and distillations and transformation of species during processing.
The data of Tao et al. w17x on gas condensates, naphthas and a crude oil, are compiled
in Table 4 and graphically depicted in Fig. 7. The origin process location. of samples
12
analyzed by Tao were not disclosed. Taos data indicate that ionic mercury was the
dominant species in the condensates examined. Hg 0 did not exceed 25% of the total in
any of the condensate samples. The dialkyl species was detected ) 10%. in some
condensates. The monoalkyl species was detected but at very low concentrations. Hg 0
was not seen in naphthas as would be expected assuming a normal distillation profile.
The more volatile Hg 0 would be expected to partition to the lighter gas fraction. RHgR
appeared to be the dominant species in one naphtha sample. Ionic forms of mercury
were seen in all of the samples.
Zettlitzer et al. w16x used two methods to measure concentrations of mercury species.
The method for monoalkylmercury HPLCUVPCOCVAA. provided suitable detection limits. The concentrations of monoalkylmercury in the condensate analyzed by
Zettlitzer were low and generally agree with the data of Tao. GCMS was used to
examine RHgR but the detection limit was high and the methodology suspect. Extracting
condensate with HCl was postulated to remove ionic and organic forms. The concentration of acid-extractable mercury was operationally defined as the difference between the
13
total amount extracted using HCl and the sum of ionic and monoalkylmercury determined independently.
Zettlitzers distributions of compounds, using operationally defined values for extracted mercury, are compiled in Table 5. The unprocessed condensate sample exhibited
a 2-ppm concentration of Hg 0 which is close to the saturation value for elemental
mercury in hydrocarbon liquids. These data do not show the dominance of ionic species
seen in the data of Tao.
Snell et al. w15x analyzed two condensates and found most of the total mercury in
ionic form. The dialkyl form accounted for approximately 10% and the monoalkyl form
less than 1%. Similarly, Schickling and Broekaert w14x analyzed two condensates and
found mostly ionic compounds. Blooms operationally defined speciation Table 6. data
account for the majority of total dissolved mercury as either Hg 0 or KCl extractable
mostly ionic..
In spite of the fact that dialkylmercury has been detected in some samples, the
concentrations found for this class of compounds see Table 4. are very low - 10 ppb.
except for one naphtha Tao. in which it was found at a concentration of approximately
14
Table 4
Analytical results for natural gas condensates, condensate naphthas and crude oil mgrl Hg. w17x
The average values of both injection modes were adopted for DMeHg, MeEtHg and DEtHg; nd not
determined; - below detection limit J. Anal. At. Spectrom., 1998, 13, 1085..
Sample
Mode
Condensate 1
Percent
Condensate 2
Percent
Condensate 3
Percent
Condensate 4
Percent
Condensate 5
Percent
Condensate naphtha 8
Percent
Condensate naphtha 9
Percent
Condensate naphtha 10
Percent
Crude oil 11
Percent
Condensate 6
Percent
Condensate 7
Percent
a
Hg 0
1.5
4.6
0.5
3.3
28.8
16.6
2.66
21.8
0.9
3.2
0.0
0.0
0.03
0.4
0.03
4.8
0.3
3.7
1.7
11.8
30.9
95.4
8.1
54.0
116
67.1
7.4
60.7
26.8
96.8
48.4
100.0
0.68
1.2
0.14
1.8
0.60
95.2
3.8
46.9
9.8
67.8
2.0
13.3
9.3
5.4
0.9
7.4
0.0
0.0
22.4
38.3
3.9
51.5
0.0
2.6
32.1
2.3
16.1
3.2
21.3
14.0
8.1
1.0
8.2
0.0
0.0
28.9
49.4
3.1
40.9
0.0
0.9
6.0
5.1
2.9
0.1
0.8
0.0
0.0
6.1
10.4
0.2
2.6
0.0
1.0
12.3
0.3
2.1
0.2
1.3
0.3
0.2
0.1
0.8
0.0
0.0
0.5
0.9
0.1
1.3
0.0
0.3
3.7
0.2
1.4
0.05
0.3
CVAAS
32.4 30.7
15.0 12.1
173
162
0.0
12.2 12.6
0.0
0.0
0.0
0.0
0.07
0.9
0.0
0.1
1.2
0.1
0.7
27.7 34.0
48.4 nd
58.5 nd
7.58 8.49
0.63 1.50
8.1 nd
14.4 nd
Sum s Hg 0 qHgClqDMeHgqMeEtHgqDEtHgqMeHgClqEtHgCl.
50 ppb. Based on the limited data, it is by no means apparent at this point in time that
dialkylmercury is prevalent in petroleum.
Stability of mercury species in synthetic gas condensate was examined by Snell et al.
w18x who demonstrated conclusively that Hg 0 and HgCl 2 react to form Hg 2 Cl 2 that is
insoluble in hydrocarbons and precipitates.
Hg 0 q HgCl 2
Hg 2 Cl 2
5.
.
HgCHq
3 and Hg CH 3 2 stable in paraffin oil stored in glass. HgCl 2 was not stable in
0
paraffin oil and Hg and HgCl 2 were unstable in natural crude oil. Blooms data
generally support those of Snells.
15
Table 5
Concentrations of mercury compounds in natural gas condensates mgrl Hg. w16x
Sample
Hg 0
HgCl 2
Other
RHgCl
Suma
Total
HgS
250
19.2
2000
39.2
200
11.8
400
30.8
400
7.8
200
11.8
644
49.5
2600
51.0
1250
73.5
6
0.5
100
2.0
50
2.9
1300
100.0
5100
100.0
1700
100.0
3500
2200
5500
400
4300
2600
Storage tank
a
16
Table 6
Operational Hg speciation in petroleum samples w13x
Sample ID
Condensate a1
Condensate a2
Crude oil a1
Crude oil a2
Crude oil a3
Crude oil a4
Crude oil a5
Crude oil a6
Crude oil a7
U
Unfiltered Hg ngrg.
0
Total
Hg
20,700
49,400
1990
4750
4610
4100
15,200
1.51
0.42
3060
U
34,500
408
1120
536
1250
2930
0.09
0.17
HgII.
CH 3 Hg
5210
36,800
821
1470
1680
1770
3110
1.01
0.41
2150
2370
291
433
377
506
489
0.39
0.02
3.74
6.24
0.25
0.26
0.27
0.62
0.45
0.15
0.11
17
18
19
phase mercury removal system to a gas separation process with both gas and liquid
feeds does not eliminate mercury in liquid products.
The amount of mercury in refinery atmospheric emissions depends on the species that
are present in the crude oil. Suspended HgS in crude oil stays with the bottom fractions
in the primary distillation. The HgS in resid and other bottom fractions used to fire
boilers is converted in combustion to volatile forms Hg 0 , HgO. that can be emitted to
the atmosphere.
Table 7
Mercury removal systems for hydrocarbons
Reactant
Substrate
Complexed form
Application
Sulfur
Metal sulfide
Iodide
PdqH 2 ; metal sulfide
Ag
Metal oxidersulfide
Carbon, Al 2 O 3
Carbon, Al 2 O 3
Carbon
Al 2 O 3
Zeolite
Oxide
HgS
HgS
HgI 2
HgS
AgrHg amalgam
HgS
Gas
Gas, liquid
Dry liquid
Liquid
Gas, light liquid
Gas, liquid
20
21
Table 8
Mercury removal systems for water
Method
Waste stream
Sulfide precipitation
Other precipitant
Ion exchange
Iron cementation
Activated carbon
Thiol resins
HgS sludge
Sludge, Hg complex
Resin, Hg 2q solution
Hg metal, iron oxide
CarbonqHg complex
ResinqHg complex
1020
110
15
0.55
0.25
- 0.1
that can achieve lower effluent mercury concentration and thus eliminate effluent
polishing. The precipitating agents form strongly insoluble complexes with mercury and
include mercaptotriazine, thiocarbonate and thiocarbamates.
Specially formulated activated carbons are used to adsorb chemisorb. elemental,
ionic and complexed mercury from water streams that do not contain significant
amounts of hydrocarbons. Activated carbons are specific and selective for mercury but
typically do not have high capacity and are used mostly for waste streams that are
relatively low in mercury content. Waste water streams can also be treated with thiol
resins that achieve very low mercury concentrations in the resin bed effluent and are
used in situations where regulatory requirements are stringent.
22
7. Waste water streams that contain high levels of mercury must be treated to
remove mercury prior to discharge thus adding significant costs to plant operational
expense.
7.1. Health and safety [33]
The major mercury-specific considerations for health and safety of workers in
petroleum processing involve exposure of workers to mercury vapor and dermal
absorption of dialkylmercury. Mercury and its compounds are neurotoxins. Inhalation of
mercury vapor, ingestion of ionic mercury or dermal absorption of mercury compounds
ultimately results in neurological dysfunction. The period of time between exposure and
exhibition of symptoms varies considerably depending upon the type absorbed mercury
species and magnitude of exposure. Chronic exposure to mercury vapor results in
psychological anomalies excitability, memory loss, insomnia, and depression. and
physical symptoms weakness, fatigue, anorexia, weight loss.. Tremors may develop in
more advanced cases. Compromise of renal function is seen in acute, high dose cases.
Analysis of blood and urine are the most common diagnostic tools for the discovery
and quantification of occupational exposure. Reference levels background level for
populations not occupationally exposed. for mercury total. in blood, urine and scalp
hair are compiled in Table 9. Assessment of worker exposure requires testing for
mercury in blood or urine at a frequency that is dictated by the exposure risks. The
concentrations of mercury in blood and urine decrease with time but not in the same
manner.
Hg 0 is readily absorbed into the blood stream via the lungs. Dermal absorption
efficiencies for elemental mercury in vapor are typically low less than 3% of the
absorbed dose. but nonetheless, must be strictly avoided. Closed space atmospheres in
equilibrium with elemental mercury deposits can acquire mercury vapor concentrations
Table 9
Reference values for total mercury concentrations in biological media general population. w1x
Matrix
Concentration
Reference
Whole blood
Fish consumption
No fish meals
Two mealsrweek
Two to four mealsrweek
18 mgrl
WHO 1990.
2.0 mgrl
4.8 mgrl
8.4 mgrl
Urine
45 mgrl
WHO 1990.
Scalp hair
2 mgrg
WHO 1990.
Fish consumption
Oncermonth
Oncer2 weeks
Oncerweek
Oncerday
1.4 mgrg
1.9 mgrg
2.5 mgrg
11.6 mgrg
23
that exceed 20 mgrm3. The most common locations for mercury accumulation are
separators and heat exchangers. Cleaning and inspection of equipment must be planned
carefully if processed hydrocarbons contain mercury total. above a few ppb. Mercury
accumulates and concentrates in vessels and will produce interior vapor concentrations
that can be much higher than the concentration of mercury in the process stream.
Accumulation mechanisms include adsorption on equipment surfaces and dissolution in
sludge.
Dialkylmercury is estimated to be many times more toxic than elemental mercury on
an equivalent weight. dose basis but exact quantification of toxicokinetics awaits
focused studies. The current OSHA standard for dialkylmercury is 0.01 mgrm3 of air
averaged over an 8-h work shift, with a ceiling level of 0.04 mgrm3. The derivation of
these limits is suspect and they should not be relied on. The concentrations of organic
mercury in unprocessed petroleum are generally assumed to be lower than for elemental
and the exposure pathways for organic mercury are more hindered in petroleum
occupations.
Estimation of the potential risk to oil-field workers due to dialkylmercury compounds
in petroleum liquids is uncertain both because of the lack of data on prevalent
concentrations and the lack of data on dermal absorption efficiency. Inhalation of large
amounts of dialkylmercury in petroleum work environments is less likely than for
elemental mercury due to its lower volatility and higher solubility in liquids. This is
offset by the higher toxicity of the dialkyl species and may not be operative in situations
involving hot work or closed space entry in warm vessels.
If dialkylmercury is discovered in substantial concentrations in crude or condensates,
dermal exposure could be a significant health risk because transdermal absorption of
organic mercury is more facile than that of elemental mercury, based on lipid solubility.
Data are lacking on the precise rates and efficiencies in both animals and humans. It is
known that petroleum workers are routinely exposed to liquid hydrocarbons that
reportedly contain significant amounts of dialkylmercury. Chronic health deficiencies
have not been reported suggesting that either the amount of dialkylmercury is over
estimated or the rate of dermal absorption is low or both.. A recent case of exposure
and death. of a laboratory worker suggests the former hypothesis is more likely w34,35x.
The toxicokinetics of RHgR has not been studied sufficiently to have definitive data
on the mechanisms of transport and elimination. It is estimated that dialkylmercury is
readily absorbed dermally and readily crosses tissue barriers. Hence, its interactions with
the body are likely more similar to CH 3 Hgq than to Hg 0 . This would mean that the
contribution of dialkylmercury to the total concentration of mercury in blood would
reflect the dose, equilibria with tissue and demethylation rate. By analogy with CH 3 Hgq,
little dialkylmercury should eliminate via urine. Monitoring total mercury in blood is the
better method for determination of occupational exposure to RHgR. Analysis of urine is
better suited to determine inhaled Hg 0 .
Ingestion of mercury is not a typical occupational hazard for workers, but ingested
mercury is often a major contributing dose factor for those whose diets contain a high
percentage of fish. The mercury compound in fish is monomethylmercury that is
bio-accumulated and bio-concentrated in piscivorous populations w36x. The predatory
marine fish species shark, tuna, swordfish, barracuda. accumulate high concentrations,
24
as do all predatory fresh water species pike, bass.. Mercury in fish that constitute a
major portion of dietary intake can contribute significantly to the total concentrations in
blood but not in urine.. The combination of dietary and occupational mercury can cause
total exposure to exceed the threshold for chronic detriment. High fish diets also can
obfuscate monitoring programs based on blood analysis for worker exposure to the
extent that occupational intake can be overestimated.
Because of the subtleties of mercury poisoning, toxic influences to neural function
can go unnoticed for very long periods of time, if they are detected at all. Chronic, low
level exposures may require years to diagnose unless exposure risks are apparent and
efforts are made to evaluate those potentially affected. Chronic mercury toxicity is
extremely difficult to diagnose from symptoms in their early stages. At the point of
conclusive symptomatic diagnosis, neuralgic impairment is usually at an advanced stage
and remediative therapies are mostly ineffective.
Atmospheres inside vessels and in the proximity of opened vessels and piping are
analyzed for mercury vapor to assist decisions on worker protection. Since the local
concentration of mercury vapor varies considerably depending upon temperature and
convection, rapid and numerous analyses are useful to understand the source and
concentration of mercury vapor in work areas. Atmospheres are typically characterized
using portable vapor analyzers w37,38x. Monitoring concentrations of mercury vapor in
plant equipment is not a routine operation in most processing plants unless there is a
historical recognition of mercury in processed hydrocarbons and prior discovery in
closed space atmospheres. The ability of portable analyzers to detect organic mercury is
uncertain.
7.2. Waste [39]
A wide variety of waste streams that contain mercury are generated in conjunction
with petroleum production and processing. The operational procedures to accumulate,
characterize and dispose of these streams likewise vary widely and depend on numerous
factors and variables. Liquid stream volumes are difficult to reduce by evaporation or
distillation because of the volatility of elemental mercury. Volume reduction by separation of mercury and compounds in solid matrices is likewise difficult to accomplish.
Waste materials that contain mercury, once identified and characterized, are treated to
remove the mercury prior to disposal of residue or debris. Treatment for disposal is not a
common practice for small volume waste streams in petroleum processing operations.
Storage of waste that contains mercury is more common in remote locations where
treatment facilities are logistically difficult to access. The US EPA is presently under
mandate to characterize major waste streams from refineries as to toxic constituents.
Some early reports w40x have examined desalter sludge and found concentrations
averaging approximately 30 ppm average of samples from three major US refineries..
Speciation of mercury compounds in petroleum processing waste has not been reported.
Removal of mercury from complex mixtures is accomplished chemically, thermally,
and sometimes physically. Physical methods vacuuming, filtration, particle separation.
rely on elemental mercurys high density and surface tension to allow segregation.
Separation of liquid mercury from soil or sludge by physical means is often warranted to
25
reduce the amount of mercury present prior to treatment by another method. Mercury
compounds typically cannot be physically separated. Chemical treatments have been
applied to soil remediation and equipment decontamination. Mercury is removed from
liquids by adding chemicals that precipitate of solid mercury compounds HgS. that can
be filtered or physically separated.
Outside the oil and gas industry, most mercury-contaminated sludge is subjected to a
thermal treatment to remove mercury, thus allowing disposal of the residuum. These
processes, referred to as roasting or retorting, vaporize mercury and mercury compounds
and condense Hg 0 . Excess heat is require to convert some compounds HgS. to the
condensable elemental form. In combustion systems, oxygen reacts with mercury
compounds to form mercuric oxide that decomposes to elemental mercury vapor. The
use of such systems to treat waste streams generated in conjunction with petroleum
processing has only recently gained acceptance in the industry.
8. Conclusions
Mercury and mercury compounds are common components of petroleum and the
products derived from it. The chemical and physical characteristics of the various
species account for the distribution of compounds in process streams. Analytical
techniques now exist to accurately determine all of the species known to be prevalent in
petroleum.
Speciation of mercury in hydrocarbon feedstocks and distilled or separated products
is necessary to determine the mechanisms that account for discharges of mercury to the
environment. As has been the case with coal-fired utilities, refineries are likely to be
closely scrutinized by regulatory bodies for mercury emissions, both atmospheric and
solid or liquid waste streams.
At present, the elemental species and ionic mercury compounds appear to be
dominant in crude oil and gas condensate. The natural abundance of organic mercury in
petroleum requires further definition. Ionic mercury in liquid hydrocarbon samples is
more prevalent than would be expected based on its concentration in coexisting phases.
This observation may be due in part to oxidation of Hg 0 in some sampling and analysis
protocols. The current data suggest monoalkylmercury compounds are not present in
produced fluids in substantial concentrations.
Removal systems that employ sorbents to react with mercury in liquid and gas
streams are available, but selection of the most effective system must be predicated on
good analytical data and on an understanding of the sorbent chemistries. Some existing
Hg removal systems for liquids do not remove the dialkyl species. Removal of mercury
from produced water or waste water streams presently consists mostly of removing
suspended hydrocarbons and solids. Chemical treatments to remove mercury from
produced water are not common in the petroleum industry.
The risks to personnel from mercury that deposits in equipment come primarily from
inhalation of vapors and from dermal absorption of dialkylmercury in condensate. The
risks due to organic mercury are uncertain and require further investigation. Health and
safety plans should be based on a quantitative analysis of risk that requires knowledge of
26
the amounts of the various mercury species that may be present. Monitoring for mercury
during maintenance and inspection activities is a key ingredient to risk assessment.
Waste that contains mercury and that originates in conjunction with petroleum
processing is difficult to segregate, store and process for disposal. Systems to treat such
waste are commercially available but seldom employed except for large volume waste
streams. Storage or burial of waste material containing mercury is a poor option that
carries residual liability to generators, but both are common practices in many remote
locations.
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