►Infrared
trace element detection
system |
►Trace Element Biology |
►Trace
Element Analysis of Food and
Diet |
►Trace-element
analysis defenition |
►Trace
Element Analysis of
Organic-Rich Samples |
►Trace
Element Analysis in
Biological Specimens |
►Trace
elements in human body
fluids and tissues |
►The
human body is composed of
what trace elements? |
|
|
|
Infrared trace element
detection system |
An infrared trace
element detection system
including an optical cell
into which the sample fluid
to be examined is introduced
and removed. Also introduced
into the optical cell is a
sample beam of infrared
radiation in a first
wavelength band which is
significantly absorbed by
the trace element and a
second wavelength band which
is not significantly
absorbed by the trace
element for passage through
the optical cell through the
sample fluid. The output
intensities of the sample
beam of radiation are
selectively detected in the
first and second wavelength
bands. The intensities of a
reference beam of the
radiation are similarly
detected in the first and
second wavelength bands. The
sensed output intensity of
the sample beam in one of
the first and second
wavelength bands is
normalized with respect to
the other and similarly, the
intensity of the reference
beam of radiation in one of
the first and second
wavelength bands is
normalized with respect to
the other. The normalized
sample beam intensity and
normalized reference beam
intensity are then compared
to provide a signal from
which the amount of trace
element in the sample fluid
can be determined. 1. An
infrared trace element
detection system comprising:
an optical cell;
means for introducing to and
removing from said optical
cell a sample fluid to be
examined;
means for introducing to
said optical cell a sample
beam of infrared radiation
including a first wavelength
band which is significantly
absorbed by the trace
element and a second
wavelength band which is not
significantly absorbed by
the trace element for
passage through said optical
cell a number of times
through the sample fluid;
a detector for selectively
detecting in said first and
second wavelength bands the
output intensities of said
sample beam of radiation
from said optical cell and
the intensities of a
reference beam of said
radiation;
means, responsive to said
means for selectively
detecting, for normalizing
the sensed output intensity
of the sample beam in one of
said first and second
wavelength bands with
respect to the other; means,
responsive to said means for
selectively detecting, for
normalizing the sensed
intensity of the reference
beam of radiation in one of
said first and second
wavelength bands with
respect to the other;
means for comparing the
normalized output intensity
and the normalized reference
intensity; and
means, responsive to said
means for comparing, for
determining the amount of
trace element in the sample
fluid.
2. The system of claim 1 in
which said means for
selectively detecting
includes means for
selectively transmitting in
said first and second
wavelength bands said sample
beam and said reference
beam.
3. The system of claim 2 in
which said means for
selectively transmitting
includes chopper means
having first filter means
for transmitting light in
said first wavelength band
and second filter means for
transmitting light in said
second wavelength band and
means for driving said
chopper means to pass said
first and second filter
means selectively through
said sample and reference
beams of infrared radiation.
4. The system of claim 3 in
which said first and second
filter means of said chopper
means are driven through the
output beam from said
optical cell.
5. The system of claim 3
further including sensor
means for sensing the
location of said chopper
means.
6. The system of claim 1 in
which said means for
normalizing the sensed
sample beam output intensity
in one of said first and
second wavelength bands with
respect to the other
includes means for dividing
one of the sensed sample
beam intensities by the
other.
7. The system of claim 1 in
which said means for
normalizing the sensed
reference beam intensity in
one of said first and second
wavelength bands with
respect to the other
includes means for dividing
one of the detected
reference beam intensities
by the other.
8. The system of claim 1 in
which said means for
comparing the normalized
sample beam intensities and
the normalized reference
intensities includes means
for dividing one of the
normalized intensities by
the other.
9. The system of claim 1 in
which said means for
determining includes means
for retrieving a stored
predetermined concentration
value of the trace element
corresponding to the
comparison parameter of the
normalized sample and
normalized reference beam
intensities.
10. The system of claim 1 in
which said means for
introducing said sample
includes a plurality of
substantially confronting
orifices arranged on
opposite sides of said
optical cell.
11. The system of claim 1 in
which said optical cell is
contained within an elongate
housing having forward and
rearward ends and includes
forward and rearward
reflector means located
proximate said forward and
rearward ends, respectively,
of said housing.
12. The system of claim 11
in which said housing
includes sealing means for
withstanding high sample
pressures.
13. The system of claim 12
in which said sealing means
are capable of withstanding
pressure of up to 850 psi.
14. The system of claim 11
in which said forward
reflector means includes a
single mirror.
15. The system of claim 11
in which said rearward
reflector means includes a
pair of mirrors with
spaced-apart centers of
curvature.
16. The system of claim 11
in which at least one of
said reflector means is
concave.
17. The system of claim 11
in which said infrared
radiation in said first and
second wavelength bands is
introduced to and exits from
said optical cell proximate
the forward end of said
housing.
18. The system of claim 1
further including means
responsive to said means for
determining for indicating
the amount of trace element
present in the sample fluid.
19. The system of claim 1
further including alarm
means for indicating when
the amount of trace element
in the sample exceeds a
predetermined level.
20. The system of claim 1 in
which said optical cell
includes a multiple
reflection optical cell.
21. An infrared trace
element detector for an
optical cell containing a
sample fluid to be examined
comprising:
means for introducing to the
optical cell a sample beam
of infrared radiation
including a first wavelength
band which is significantly
absorbed by the trace
element and a second
wavelength band which is not
significantly absorbed by
the trace element for
passage through said optical
cell through the sample
fluid;
a detector means for
selectively detecting in
said first and second
wavelength bands the output
intensities of said sample
beam of radiation from said
optical cell and the
intensities of a reference
beam of said radiation;
means, responsive to said
means for selectively
detecting, for normalizing
the sensed output intensity
of the sample beam in one of
said first and second
wavelength bands with
respect to the other;
means, responsive to said
means for detecting, for
normalizing the sensed
intensity of the reference
beam in one of said first
and second wavelength bands
with respect to the other;
means for comparing the
normalized sample beam
intensity and the normalized
reference beam intensities;
and
means, responsive to said
means for comparing, for
determining the amount of
trace element in the sample
fluid.
22. A fluid sample
transmission system for an
optical detection system
comprising:
an optical cell for
receiving a sample beam of
radiation; and
a plurality of substantially
confronting orifices
arranged in opposite sides
of said optical cell for
introducing sample fluid to
said cell.
23. An infrared trace
element detection system
comprising:
an optical cell;
means for introducing to and
removing from said optical
cell a sample fluid to be
examined including a
plurality of substantially
confronting orifices
arranged in opposite sides
of said optical cell;
means for introducing to
said optical cell a sample
beam of infrared radiation
including a first wavelength
band which is significantly
absorbed by the trace
element and a second
wavelength band which is not
significantly absorbed by
the trace element for
passage through said optical
cell through the sample
fluid;
a detector for selectively
detecting in said first and
second wavelength bands the
output intensities of said
sample beam of radiation
from said optical cell and
the intensities of a
reference beam of said
infrared radiation;
means responsive to said
detector for normalizing the
sensed output intensity of
the sample beam in one of
said first and second
wavelength bands with
respect to the other;
means responsive to said
detector for normalizing the
sensed intensity of the
reference beam in one of
said first and second
wavelength bands with
respect to the other; means
for comparing the normalized
sample beam intensity and
the normalized reference
beam intensity; and
means responsive to said
means for comparing for
determining the amount of
trace element in the sample
fluid.
Description:FIELD OF
INVENTION
This invention relates to an
infrared trace element
detection system, and in
particular to a system which
compares the intensity in
two different spectral bands
of a sample beam, reflected
a number of times through
the sample, and a reference
beam.
BACKGROUND OF INVENTION
Conventional measurement of
trace elements in gas
samples has presented a
number of difficulties. For
example, to detect the
amount of water present in a
sample of the helium coolant
from a nuclear reactor,
typically the helium sample
is passed over a mirror
which is cooled so that any
water present in the gas
condenses. Light is passed
through the sample and
directed at the mirror; as
the water condenses a change
in reflection indicates the
amount of water present in
the gas. However, the
response time required to
sense the water,
particularly at very low
concentrations, is
relatively long.
Additionally, the system is
complex and requires
considerable maintenance.
Refrigeration is required,
the mirror periodically
becomes pitted and water
must be removed from the
mirror between tests making
for low response time and
repetition rate.
Infrared detectors may be
employed to monitor humidity
and other trace elements. In
such systems radiation
including a first wavelength
band which is significantly
absorbed by the trace
element and a second
wavelength band which is not
significantly absorbed, is
passed through a gas sample.
The output intensities of
the respective bands are
compared to provide a
measure of the concentration
of the trace element in the
sample. Problems arise,
however, as the filters or
other means for providing
the individual wavelength
bands of radiation age or
become contaminated. This
tends to cause variations in
the measured values of the
compared intensities that
are not due to changes in
concentration. To avoid
erroneous concentration
measurements frequent
calibration is therefore
required.
Further disadvantages are
exhibited by optical cells
which hold the sample gas
for testing. For example, to
accurately and continuously
monitor the sample gas a
smooth uninterrupted gas
flow is desired in the area
of the introduced beam of
radiation. However, present
techniques for introducing
the sample gas into the
optical cell tend to
generate considerable
turbulence and undesirable
recirculation within the
cell which inhibit a smooth
uninterrupted flow and
permit dirt and other
contaminants to collect on
the mirrors of the optical
cell. This interferes with
proper circulation of the
sample gas and causes
inaccurate concentration
measurements.
SUMMARY OF INVENTION
It is therefore an object of
this invention to provide an
improved infrared trace
element detection system.
It is a further object of
this invention to provide an
infrared trace element
detection system which
yields extremely accurate
measurements and which
exhibits an improved
response time, particularly
when monitoring relatively
low-concentration samples.
It is a further object of
this invention to provide an
infrared trace element
detection system which
avoids detector drift and
measurement errors caused by
such drift without requiring
frequent calibration.
It is a further object of
this invention to provide an
infrared trace element
detection system which has a
long life and low service
requirements.
It is a further object of
this invention to provide an
infrared trace element
detection system which
employs rugged optics
suitable for use in high
pressure/high temperature
environments such as nuclear
reactors.
It is a further object of
this invention to provide an
infrared trace element
detection system having a
smooth uninterrupted flow of
sample fluid in the area of
the infrared beam to provide
timely, rapid, continuous
monitoring of the sample
fluid and reduce contaminant
buildup on the mirrors of
the optical cell.
This invention results from
a realization that the
infrared detection of trace
elements in a fluid sample
may be accomplished with
much less detector drift and
resultant measurement error
by normalizing the output
intensity of the radiation
in a first wavelength band
which is substantially
absorbed by the trace
element and a second
wavelength band which is not
substantially absorbed by
the trace element;
normalizing the absorbed and
nonabsorbed intensities of a
second reference beam of the
infrared radiation; and then
comparing two normalized
intensities. In this manner
any error which is
introduced by either the
absorbing or nonabsorbing
filter is introduced into
both the sample and
reference beams and
therefore corrected when the
normalized intensities of
the respective beams are
compared.
This invention results from
the additional realization
that accuracy and
performance of an infrared
trace element detection
system may be enhanced even
further by introducing
sample fluid into the system
through a construction of
confronting orifices which
rapidly replenishes the
fluid in the beam path
within the cell and reduces
the collection of stagnant
gas in the vicinity of the
beam path.
This invention features an
infrared trace element
detection system which
includes an optical cell and
means for introducing to and
removing from said optical
cell a sample fluid to be
examined. There are means
for introducing to the
optical cell a sample beam
of infrared radiation in a
first wavelength band which
is significantly absorbed by
the trace element and a
second wavelength band which
is not significantly
absorbed by the trace
element for passage through
the optical cell through the
sample fluid. There are
means for selectively
detecting in the first and
second wavelength bands the
output intensities of the
sample beam of radiation
from the optical cell and
the intensities of a
reference beam of the
radiation. There are means,
responsive to the means for
selectively detecting, for
normalizing the sensed
output intensity of the
sample beam in one of the
first and second wavelength
bands with respect to the
other. Means, responsive to
the means for selectively
detecting, are also provided
for normalizing the sensed
intensity of the reference
beam in one of the first and
second wavelength bands with
respect to the other. There
are means for comparing the
normalized output intensity
and the normalized reference
intensity and means,
responsive to the means for
comparing, for determining
the amount of trace element
in the sample fluid.
In a preferred embodiment
the means for selectively
detecting includes a single
detector. The means for
selectively detecting may
include chopper means for
selectively transmitting in
the first and second
wavelength bands the sample
beam and reference beam.
Such means may include
chopper means having first
and second filter means and
means for driving the
chopper means to pass the
first and second filter
means selectively through
the sample and reference
beams of infrared radiation.
Preferably, the first and
second filter means of the
chopper device are driven
through the output beam from
the optical cell. Sensor
means may be provided for
sensing the location of the
chopper device.
The means for normalizing
the sensed sample beam
output intensity may include
means for dividing one of
the sensed sample beam
intensities by the other.
The means for normalizing
the detected reference beam
intensity may include means
for dividing one of the
detected reference beam
intensities by the other.
The means for comparing the
normalized sample beam
intensity and the normalized
reference beam intensity may
include means for dividing
one of the normalized
intensities by the other.
The means for determining
may include means for
retrieving a stored
predetermined concentration
of the trace element
corresponding to the
comparison parameter of the
normalized output and
normalized reference
intensities.
Means may be provided for
indicating the amount of
trace element detected in
the sample fluid and alarm
means may be activated when
the amount of trace element
exceeds a predetermined
level.
The means for introducing
the sample preferably
includes a plurality of
substantially confronting
orifices arranged on
opposite sides of the
optical cell. The optical
cell may be contained within
an elongate housing having
forward and rearward ends.
The housing may include
sealing means for
withstanding high gas sample
pressures of, for example,
up to 850 psi. The optical
cell may include forward and
rearward reflector means
located proximate the
forward and rearward ends,
respectively, of the
housing. The forward
reflector means may include
a single mirror and the
rearward reflector means may
include a pair of mirrors
having spaced-apart centers
of curvature. Typically, at
least one of the reflector
means is concave. The
infrared radiation in the
first and second wavelength
bands is preferably
introduced through and exits
from the optical cell
proximate the forward end of
the housing. The optical
cell may include a multiple
reflection optical cell.
DISCLOSURE OF PREFERRED
EMBODIMENT
Other objects, features and
advantages will occur from
the following description of
a preferred embodiment and
the accompanying drawings,
in which:
FIG. 1 is a simplified
axonometric view of the
optical elements of the
infrared trace element
detection system of this
invention;
FIG. 2 is a simplified
schematic view of certain of
the optical elements of the
detection system and the
paths taken by the reference
and sample beams;
FIG. 3 is a top view of the
trace element detection
system housing;
FIG. 4 is a graph
illustrating the detected
output and reference
intensities versus the
position of the chopper
device;
FIG. 5 is a schematic view
of signal processor for
normalizing and comparing
the sensed detector
intensities and for
determining the trace
element concentration and a
circuit for sensing the
location of the chopper
device;
FIG. 6 is a graph
illustrating curves
representing the measured
concentration of water
versus the ratio of the
normalized detector
intensities at various
pressures;
FIG. 7 is a flow chart for
resolving the proportion of
trace element in the sample
gas;
FIG. 8 is a schematic
diagram of a preferred
alternative signal processor
which digitally processes
the detected intensity
signals to determine the
proportion of trace element
in the gas sample;
FIG. 9 is a side
cross-sectional view of the
optical cell and housing of
FIG. 3;
FIG. 10 is a cross-sectional
view of the orifices for
introducing sample fluid to
the optical cell taken along
line 10--10 of FIG. 11; and
FIG. 11 is a cross-sectional
view taken along line 11--11
of FIG. 10.
An infrared trace element
detection system according
to this invention may be
accomplished using an
optical cell. A preferred
cell is a muliple reflection
optical cell such as a White
cell. Alternatively an
optical cell which provides
only a single reflecion or
no reflections at all may be
employed. A sample fluid,
such as the helium coolant
from a nuclear reactor, is
introduced to and removed
from the optical cell so
that the sample may be
monitored for the presence
of water or other trace
elements.
The multiple reflection
optical cell receives a
sample beam of infrared
radiation including a first
wavelength band which is
significantly absorbed by
the trace element and a
second wavelength band which
is not significantly
absorbed by the trace
element. The sample beam is
reflected by the multiple
reflection optical cell a
number of times through the
sample fluid. A preferred
infrared source includes a
resistively heated coil of
wire, such as the Kanthal
wire wound source
manufactured by Infrared
Industries, Inc., which
provides a spectrally smooth
broadband of radiation.
The output intensity of the
sample beam of radiation
from the multiple reflection
optical unit as well as the
intensity of a reference
beam of the infrared
radiation are selectively
detected in the first and
second wavelength bands. The
selective detecting
typically is accomplished
with a chopper or other
means for selectively
transmitting in the first
and second wavelength bands
the sample beam and the
reference beam. Although a
separate chopper may be
employed for each beam, it
is preferred that a single
chopper device having first
and second filters be used
for both beams. The chopper
is driven to pass the first
and second filters
selectively through the
sample and reference beams
of radiation. For example,
the chopper device may
include a rotatably driven
aluminum disk with narrow
band filters located 180°
apart. In monitoring a
helium sample for the
presence of water vapor a
desirable infrared absorbing
first band includes the
wavelength 2.51-2.63 μm and
the nonabsorbing second
wavelength band may include
the wavelengths 2.4-2.5 μm.
Preferably, the first and
second filters of the
chopper device are driven
through the output beam from
the multiple reflection
optical unit. Alternatively
the sample beam may be
chopped into alternating
absorbing and nonabsorbing
bands prior to introduction
to the optical unit. It is
preferred that a single
detector be provided for
both the sample and
reference beams. However,
each of those beams may
employ a separate detector.
Typically a lead sulfide
detector or other suitable
photodetector is employed.
The intensity of the sample
beam in, typically, the
first band is divided by,
subtracted from or otherwise
normalized with respect to
the intensity in the second
band. Similarly the sensed
intensity of the reference
beam in preferably the first
wavelength band is divided
by, subtracted from or
otherwise normalized with
respect to its sensed
intensity in the second
band. The normalized sample
beam intensity and
normalized reference beam
intensity are then compared
by division, subtraction or
otherwise and a signal
representative of this
comparison parameter is used
to determine the amount of
trace element in the sample
fluid. The amount of trace
element may be calculated
from the compared value. A
sensor may be provided for
sensing the location of the
chopper so that the detected
intensities may be processed
in the proper sequence.
Alternatively, the
comparison parameter may be
used to retrieve from a
memory a corresponding value
of the trace element.
The temperature and/or
pressure of the sample fluid
may also be sensed and used
by a retrieval circuit or
calculation circuit for
determining the amount of
the trace element in the
sample at the sensed
temperature and/or pressure.
The determined amount may be
indicated on, for example, a
dial or readout, and if the
trace element exceeds a
predetermined amount an
audio or visual alarm may be
activated.
By dividing or otherwise
comparing the normalized
intensity of a sample beam
with the normalized
intensity of a reference
beam the present invention
overcomes the problem of
instrument drift. If, for
example, the filter which
transmits the nonabsorbed
wavelength band collects
dirt or otherwise becomes
contaminated at a rate
different than the filter
which transmits the absorbed
wavelength band, the
resulting changes in the
normalized intensity in the
first and second wavelength
bands are exhibited by both
the sample beam and the
reference beam. Therefore,
the compared value remains
constant and the system
remains calibrated.
This invention also features
a fluid sample transmission
system for introducing fluid
sample into an optical cell
such as the multiple
reflection optical cell
previously described. The
sample is introduced through
a plurality of substantially
confronting orifices
arranged on opposite sides
of the optical cell. By
"substantially confronting"
it is meant that the
opposing orifices may be
either aligned or staggered
relative to each other.
Typically, the White cell or
other optical cell used in
this invention is contained
within an elongate housing
having forward and rearward
ends. The multiple
reflection optical unit
includes forward and
rearward reflector means
located proximate the
forward and rearward ends
respectively of the housing.
Typically, the forward
reflector means includes a
single mirror and the
rearward reflector means
includes a pair of mirrors
having spaced apart centers
of curvature. At least one
of the reflectors may be
concave. The sample beam of
infrared radiation is
preferably introduced to and
exits from the multiple
reflector optical cell
proximate the forward end of
the housing. The device may
be arranged to permit one or
many passes of the sample
beam through the optical
cell. Limiting the number of
passes lessens degradation
of the signal and simplifies
reflector and detector
alignment.
The substantially
confronting orifices are
arranged in the opposite
sides of the optical unit so
that fluid is introduced to
the optical cell to create a
smooth and uninterrupted
flow in the area of the
sample beam. This enables
the sample fluid to be
continuously circulated and
monitored. Eddies which trap
pockets of gas within the
cell are reduced and
contaminant buildup on the
mirrors of the optical cell
is lessened.
There is shown in FIG. 1 the
optical elements of an
infrared trace element
detection system according
to this invention. The
sample fluid being monitored
is introduced, as described
more fully below, to a
multiple reflection optical
cell 12 which includes a
forward mirror 14 and an
opposing pair of
spaced-apart concave
rearward mirrors 16, 18
which face the front mirror.
Although the embodiments
discussed herein employ a
multiple reflection cell, an
optical cell employing only
a single reflection or a
single pass with no
reflections may instead be
used in the practice of the
invention.
An infrared detection unit
20 features a source 22 of
infrared radiation 24
including a first wavelength
band which is significantly
absorbed by the trace
element being monitored in
the sample fluid and a
second wavelength band which
is not significantly
absorbed by the trace
element. Radiation 24 is
transmitted through lens 26
to a beam splitter 28 which
splits the radiation into a
sample beam 30 and a
reference beam 32. Sample
beam 30 is reflected from
mirror 34 and introduced
through window 36 to optical
cell 12. Therein, beam 30
passes over shoulder38 of
mirror 14 and is reflected
approximately 20 times
between mirror 14 and
rearward mirrors 16 and 18
respectively. Beam 30
finally exits cell 12 over
shoulder 40 of mirror 14 and
through window 42, and is
projected from the cell as
output beam 30a.
A chopper wheel 44,
rotatable about axis 45,
selectively transmits both
output beam 30a and
reference beam 32 in the
first absorbing and second
nonabsorbing wavelength
bands. Chopper 44 includes a
first filter 46 which
transmits only radiation in
the first band and a second
filter 48, diametrically
opposed to filter 46, which
transmits only radiation in
the second band. Chopper
wheel 44 is rotated in the
direction of arrow 50 so
that filters 46 and 48 are
alternately passed through
both sample output beam 30a
and reference beam 32. For
example, first filter 46 is
shown passing through output
beam 30a. This causes
radiation in the first
absorbing wavelength band to
be transmitted through the
filter and through a lens 52
disposed behind the chopper
wheel. Radiation 30b in the
first wavelength band is
then transmitted through
beam splitter 54 and sensed
by detector 56. As this
occurs, chopper wheel 44
blocks transmission of
reference beam 32 and, as a
result, the intensity of
that beam is not measured.
The chopper wheel continues
rotating and after
one-quarter turn first
filter 46 is at the position
indicated in phantom. The
first wavelength band of the
reference beam is then
transmitted through filter
46. The transmitted portion
32b of the reference beam is
reflected from mirror 58 and
directed through lens 60 to
beam splitter 54 where it is
reflected and measured by
detector 56. At the same
time, transmission of the
sample output beam 30a is
blocked by chopper 44 and as
a result only the intensity
of the reference beam in the
first wavelength band is
measured.
An additional one-quarter
turn places filter 48 in the
path of sample output beam
30a. Accordingly, the second
nonabsorbing wavelength band
of the sample beam is
transmitted through the
chopper and sensed by
detector 56. Filter 48 is
then rotated through the
path of reference beam 32 so
that the intensity of the
reference beam in the second
wavelength band may be
similarly detected.
With each revolution of
chopper 44 detector 56
successively senses the
intensities of the sample
output beam 30a and
reference beam 32 in the
first wavelength band and
the intensities of the
sample and reference beams
in the second wavelength
band. Between each quarter
turn the sample and
reference beams are both
blocked by the chopper and
no infrared intensity is
detected.
The arrangement of the paths
which the reference beam 32
and sample beam 30 travel
are shown in somewhat more
detail in plan view in FIG.
2. After leaving source 22
broadband radiation 24
passes through lens 26 and
is split by beam splitter 28
into sample beam 30 and
reference beam 32. Mirror 34
has a reflective surface 64
and is a part of a
ball-and-socket mirror
assembly 66. Assembly 66
includes a base 68 having a
socket 69 which receives the
circularly contoured bearing
surfaces 70 of mirror 34. By
adjusting screws 71 and 72
the angle of reflective
surface 64 of mirror 34 may
be set. In this manner the
direction of sample beam 30
is adjusted to achieve the
desired number of
reflections within optical
cell 12.
Sample beam 30 enters
optical cell 12 through
window 36 and passes over
the respective shoulders 38
and 40 of mirror 14 as it
enters and exits the optical
cell. After exiting through
window 42 of cell 12 sample
output beam 30a encounters
the rotating chopper wheel,
not shown, and as the
filters, e.g., filter 46,
are alternately driven
through the sample output
beam, radiation is
alternately transmitted in
the selected first
wavelength band and the
second wavelength band. The
transmitted wavelength band
30b passes through lens 52
which causes the beam to
converge. This converging
beam portion 30b is
transmitted through beam
splitter 54 and its
intensity is sensed by
detector 56.
Reference beam 32 is
reflected from surface 76 of
beam splitter 28 and the
transmitted wavelength
portion 32b is directed
toward steering mirror 58.
As with mirror 34, mirror 58
is included in a
ball-and-socket mirror
assembly 66 which enables
the angle of reflective
surface 64 of mirror 58 and
therefore the direction of
reflected reference beam
portion 32b to be adjusted
by adjusting screws 71 and
72. Reference beam portion
32b is reflected from the
surface 64 of mirror 58
through lens 60. The beam is
then reflected from front
surface 78 of beam splitter
54 onto detector 56 which
measures the intensity of
the reference beam portion
32b transmitted by the
chopper.
A housing 80 for the
infrared trace element
detection system is shown in
FIG. 3. The entire structure
is mounted on a yoke 82 and
includes a detector housing
84, an optical cell housing
86 and an infrared source
housing 88. Detector housing
84 includes a flange 90 at
one end to which a cover 92
is connected by bolts 94. A
second flange 100 at the
other end of housing 84 is
similarly connected by bolts
98 to a flange 96 which also
supports the optical
components of FIGS. 1 and 2.
Ports 93 and 95 are provided
into housing 84 to conduct
wiring from the detector to
an external signal
processor.
Optical cell housing 86
includes, at one end, a
flange 102 which is attached
to flange 96 by bolts 104.
Typically, a high-pressure
seal, not shown, such as a
copper Varian gasket, is
disposed between flange 102
and flange 96 to prevent
leakage of sample fluid from
the multiple reflection
optical unit. The opposite
end of housing 86 includes a
flange 106 and end cover 108
which also may include a
high pressure seal,
effective for withstanding
gas pressures of up to 850
psi, interposed between
them. Flange 106 and cover
108 are secured together by
bolts 110. Sample fluid is
introduced, as described
more fully below, through
inlet 152.
Infrared source housing 88
includes a flange 112 and
cover 114 which are
connected by bolts 116. A
port 118 conducts wiring
connected to the infrared
radiation source.
The intensity measured by
the detector during the
course of a single
representative rotation of
the chopper wheel is shown
in FIG. 4. For example, with
first filter 46 at 0° (i.e.,
passing through sample
output beam 30a as shown in
FIG. 1) the intensity A of
the sample output beam from
the multiple reflection
optical cell 12 in the first
(absorbing) wavelength band
is measured. The chopper
then rotates 90° so that
filter 46 is in the position
shown in phantom in FIG. 1.
The absorbing wavelength
band of the reference beam
32 is thereby transmitted
through filter 46 and its
intensity B, FIG. 4, is
measured.
At the 180° position the
second filter 48 is passed
through sample output beam
30a, the second
(nonabsorbing) wavelength
band of this beam is
transmitted through the
filter and its intensity C,
FIG. 4, is sensed by the
detector. A further rotation
of 90° of the chopper wheel
(i.e., at the 270° position)
places the second filter 48
in the path of reference
beam 32. As a result, the
nonabsorbing wavelength band
of the reference beam is
transmitted and its
intensity D is measured by
the detector.
As indicated in FIG. 4, in
the intervals between
filters 46 and 48 the
chopper wheel completely
blocks the passage of the
sample and reference beams.
No infrared radiation is
transmitted and the measured
intensity is zero.
A signal processor 120 for
processing the detected
intensity signals A, B, C,
and D is shown in FIG. 5.
The respective signals are
provided from detector 56 to
a switching circuit 121. A
sensor 122 detects
appropriate indicia 125
disposed around the
circumference of wheel 44,
and provides a signal to
circuit 121 which identifies
the signal received from
detector 56 as either signal
A, B, C or D. The switching
circuit feeds signals A and
C, representing the
intensities of the sample
output beam in the absorbing
and nonabsorbing wavelength
bands respectively, to
divider circuit 123 where
they are divided to provide
normalized signal A/C.
Similarly, signals B and D,
representing the intensities
of the reference beam in the
absorbing and nonabsorbing
wavelength bands,
respectively, are provided
by switching circuit 121 to
a divider circuit 124 where
they are divided to yield
the normalized signal B/D.
Signals A/C and B/D are
divided in divider circuit
126 to yield signal R (e.g.,
(A×D)/(B×C)). Signal R is
provided along with signals
indicative of the
temperature T and the
pressure P of the fluid
sample to a table retrieval
circuit 128 where the
proportion of water or other
trace element being measured
in the sample is retrieved
from calibration curves,
described more fully in
connection with FIG. 6,
which are stored in the
memory of the circuit.
Alternatively, the
proportion of trace element
in the fluid sample may be
determined by entering
signal R into a calculation
circuit 130 where a
conventional algorithm is
employed to calculate the
proportion as described in
connection with FIG. 7. The
determined concentration of
trace element is indicated
on a readout 132 and if the
proportion reaches an
undesirably high level, an
alarm 134 is activated.
A sensor is not required if
the filters are arranged on
the chopper at an interval
other than 180°. For
example, if they are
separated by 135°, signals
A, B, C, and D are provided
at 0°, 90°, 135° and 225°,
respectively. This uneven
spacing serves to identify
the respective signals and
eliminates the need for a
sensor.
A calibration curve, FIG. 6,
may be used by table
retrieval circuit 128 for
determining stored water
proportion values for a
sample of high-pressure
helium. Values along the x
axis represent the divider
circuit output signal R
provided to the retrieval
circuit 128. Values along
the y axis indicate the
concentration of water in
the helium sample in parts
per million. Curve 142
indicates the calibrated
concentration values at a
pressure of 200 psi; curve
144 indicates such values at
400 psi; and curve 146
indicates the concentrations
at 800 psi. These values are
obtained in a helium sample
which is maintained at a
constant temperature of 110°
F. Similarly shaped curves
with different
concentrations are obtained
at different temperatures.
Each of these calibrated
curves is compiled by
employing a helium sample
having known concentrations
of water and predetermined
temperatures and pressures
and measuring the values R
for such samples.
Preferably logic may be
employed in circuit 130 to
calculate the proportion of
trace element is shown in
FIG. 7. Table 191 is
provided with known
combinations of values of
temperature T, pressure P,
ratio R and X, where X, a
function of T, P and R,
equals the log of the
concentrations C. Table 191
thus expresses the
functional dependence of X
on T, P and R. Known
temperatures, pressures and
R values T 1 , T 2 , P 1 , P
2 and R 1 , R 2 which bound
the detected values T', P'
and R', respectively, are
retrieved from Table 191,
step 192. These values are
used to perform known three
dimensional linear
interpolation, steps 193,
194 and 195 to calculate the
value of X which is
associated with T', P' and
R'. Concentration is
calculated, step 196, by
re-exponentiating X and
multiplying e x by C o where
C o is a typically constant
predetermined scaling
factor.
In an alternative preferred
embodiment the intensity
signals may be alternatively
processed digitally as shown
in FIG. 8. Detector 56a is
connected to a 100-volt bias
supply 210 through a
resistor 212. Because the
noise and sensitivity of
detector 56a is strongly
temperature dependent the
detector includes a
thermistor which provides a
temperature signal t over
line 214 and through
amplifier 216 to
microcontroller 218. A
thermocouple 220 measures
the temperature of the
incoming high pressure gas
entering optical cell 12,
FIGS. 3, 9. Its signal T
proceeds over line 222
through thermocouple signal
conditioner 223 and
amplifier 224 to
microcontroller 218. A
strain gauge 228 detects the
pressure of the incoming gas
sample and provides a signal
P representative of that
pressure over line 230 and
through amplifier 232 to the
microcontroller.
The absorption signals A, B,
C and D provided by detector
56a are amplified and
buffered by a preamp 236 and
then directed through an
amplifier 238, a sample and
hold circuit 240 and an A/D
converter 242. The signals
are then transmitted through
digital data buffers 243,
244 to the input of
microcontroller 218. As a
result each signal A-D is
converted to a respective
fourteen bit digital signal
AD, BD, CD, DD.
The microcontroller is
programmed in a conventional
manner to process the
signals so that signal AD is
normalized with respect to
signal CD, signal BD is
normalized with respect to
signal DD and the normalized
intensity signals are
compared to provide a signal
R, not shown. The steps of
such a program may include,
for example, the division
steps performed by the
divider circuits described
in FIG. 5. The signal R
derived in this manner is
then employed in either a
table retrieval circuit or a
calculation circuit in
microcontroller 218, which
operate analogously to the
description in FIGS. 6 and 7
to provide the detected
proportion of trace element
to display 132a. Alarm 134a
sounds when the
concentration exceeds a
predetermined level.
In order to prevent the heat
generated by motor 260 and
the ambient environment from
disrupting the concentration
determination the detector
includes and is cooled by a
solid state heat pump, not
shown. Microcontroller 218
reads detector temperature t
and feeds back a control
signal C through buffer 245,
low pass filter 246 and
power operational amplifier
248 which operates the heat
pump when the detector
temperature t is too high.
Detector 56a and its
associated optics are
enclosed in a pressure
vessel, housing 84, FIG. 3,
which is sealed to prevent
introduction of high
pressure sample gas into the
surrounding air through a
leak or break in the windows
36 and 42. A second pressure
sensor 250 monitors pressure
in detector housing 84 and
provides a signal p through
buffer 252 to
microcontroller 218. When
that pressure exceeds a
predetermined level an
alarm, not shown, may be
sounded.
Again, the sample and
reference beams of infrared
radiation are chopped into
their respective wavelength
bands by a chopper wheel 44.
The wheel is driven by a
stepper motor 260 which is
controlled by the
microcontroller through a
drive circuit 262. Sensor
122a senses indicia 125a on
the wheel and provides a
signal to microcontroller
218 over line 264 which
indicates to the
microcontroller which signal
AD-DD it is receiving.
Sample fluid is introduced
to and removed from optical
cell 12 as shown in FIGS.
9-11. Optical cell 12, FIG.
9, includes a chamber 150
which extends generally from
the forward end to the
rearward end of housing
portion 86. Forward mirror
14 and rearward mirrors 16
and 18 (only mirror 18 is
shown) are mounted at
opposite ends of chamber
150.
A fluid inlet 152 extends
through cover 108 of housing
portion 86 and communicates
via nipple 154 with an
elongate channel 156 that
extends generally from the
rearward end to the forward
end of housing 86. An
annular channel 158 is
interconnected with elongate
channel 156 and surrounds
the forward end of optical
chamber 150. A plurality of
substantially confronting
orifices 160 are connected
to annular channel 158 and
are arranged in opposite
sides of optical chamber
150. An annular seal 161 is
disposed peripherally about
channel 158.
Sample fluid is introduced
via inlet 152 and travels
through channel 156 toward
the forward end of the
optical cell. The sample
fluid is conducted through
annular channel 158 and
orifices 160 into the
interior of optical chamber
150. Leakage from channel
158 is prevented by seal
161. The sample fluid
travels through the chamber
toward the rearward end of
the cell, past mirrors 16
and 18 and exits the optical
cell through outlet 164
which extends through cover
108 of housing 86.
Alternatively, the inlet may
be provided proximate the
top and the outlet proximate
the bottom of the housing.
The opposing rows of
orifices 160, FIG. 10, which
are provided in both the
upper and lower surfaces of
chamber 150 immediately in
front of the face of mirror
14 may be offset by, for
example, 1/32 inch. This
arrangement creates a smooth
uninterrupted fluid flow
165, FIG. 11, in the area in
which the sample beam is
introduced into the optical
cell. Introducing the sample
fluid through the
substantially confronting
orifices 160 tends to
disrupt and minimize the
formation of eddies 170.
This reduces the amount of
stagnant sample fluid
lingering in the vicinity of
mirror 14. As a result, as
the sample beam is
introduced into the optical
chamber, for example, past
shoulder 40 of lens 14, and
similarly as it is reflected
back from the rearward
mirrors toward the face of
mirror 14, the beam
encounters generally fresh
sample fluid. This enhances
the rapidity of the
measurement of a change in
trace element concentration.
Additionally, since it is
designed to reduce
recirculation and stagnation
of the introduced sample
fluid, less dirt and dust
collects on the surface of
mirror 14.
In operation, sample fluid
is introduced with reduced
recirculation into optical
cell 12 as shown in FIG. 11.
Infrared radiation 24, FIGS.
1 and 2, is split into
reference sample beam 30 and
the sample beam is
introduced into the optical
cell where it undergoes
multiple reflections. The
sample output beam 30a and
reference beam 32 are then
chopped by chopper 44 so
that at 90° intervals the
intensities of the sample
and reference beams in the
first and second wavelength
bands, respectively, are
measured by detector 56.
Those intensities A, B, C
and D are fed to signal
processor 120, FIG. 6,
wherein the absorbed
intensity of the sample beam
is normalized relative to
the nonabsorbed intensity by
divider circuit 122. The
absorbed intensity of the
reference beam is similarly
normalized with respect to
the nonabsorbed intensity of
the reference beam in
divider circuit 124 and
those respective ratios are
compared in divider circuit
126 to yield a ratio signal
R which compensates for
filter contamination and
detector errors. Signal R is
then employed in a table
retrieval circuit or
calculation circuit to
determine the amount of
trace element in the sample
fluid. That amount is
indicated by readout 132 and
if excessive amounts are
indicated an alarm 134 is
activated. |
Article Source: |
http://www.freepatentsonline.com/4785184.html |
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|
Trace Element Analysis
of Organic-Rich Samples
|
Organic-rich materials
have a variety of uses as
fuels, for example coal,
petroleum coke and biomass,
together with a range of
waste materials used as
alternative fuels; and as
fertilizers, for example
compost and sewerage sludge.
Accurate trace element
analysis of these materials
is becoming increasingly
important as governments
tighten regulations to
minimize and control
contamination and
environmental pollution and
promote the use of renewable
sources of energy. Some
industries are expected to
replace up to 20% of their
traditional fuels by biomass
by 2010. This means that
large quantities of samples
will need to be analyzed for
process control and to meet
governmental regulations on
biomass types and
compositions. However, one
of the main problems faced
when analyzing such a
diverse range of
organic-rich materials is
the availability of suitable
reference materials.
Features of XRF Trace
Element Hardware and
Software
The Axios is a fully
integrated
wavelength-dispersive XRF
analyzer, consisting of a
spectrometer, X-Y sample
handler and software.
Designed to provide
accuracy, precision and sub-ppm
detection limits for many
elements, the Axios, coupled
with the unique Pro-Trace
software and standards,
provides the highest quality
trace element analysis (U to
Sc), and targets a wide
range of materials of
geological and environmental
significance.
Pro-Trace standards in
special storage cups and
case
25 standards, 2 monitors
High purity constituents
Robust pressed powders in
aluminium rings
Dished storage cups prevent
contamination of standards |
Article Source: |
http://www.azom.com/details.asp?ArticleID=4771 |
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|
Trace Element Biology |
Impressive strides are
being made in the
understanding of trace
element metabolism and
function. This is
underscored by the many
contributions in these
proceedings. However, not so
impressive are: i) the
precise recognition of mild
trace element deficiencies
and how to establish their
functional consequences,
possibly confounded by
concurrent trace element
inadequacies, are difficult
to assess, ii) approaches to
the quantitative
determination of
requirements for trace
elements remain
unsatisfactory and archaic,
in so many ways, iii) our
understanding of the extent
of the biological basis for
the variation in
requirements among
apparently similar
individuals is poor, and iv)
much needs to be learned
about the quantitative
extent to which genetic,
epigenetic and dietary
factors interact to
determine the nutritional
phenotype. Some ideas are
presented as to how we might
embrace, in the context of a
reconstructive approach, the
exciting new knowledge and
related techniques emerging
during the postgenome era
and develop new paradigms
for assessing trace element
needs and status, and for
establishing effective
nutrient intake under
different conditions of
complex genotype-environment
interactions. Metabolites
are functional cellular
entities and I also urge a
vigorous application of
metabolomics and of
metabolic profiling that is
closely linked with
genomics, proteomics, trace
element kinetics and system
analysis, as components of
the new integrative
paradigm. We need to
understand the system and
its strategy, not only the
molecular details of its
component parts and its
individual controls. An
interdisciplinary research
and teaching enterprise will
be necessary to best achieve
this aim. All of this is
related to our common goal
to promote, through expanded
biological knowledge and its
effective application, the
enhanced role of trace
elements for human
well-being.
Trace element deficiencies.
The first entry in Table 1
begins with a recognition of
the difficulties still faced
in identifying mild trace
element deficiencies and
their functional
consequences, perhaps
further confounded by other
specific but concurrent
inadequacies. It is
relevant, in this context,
to mention two recent
observations: i) restoration
of an adequate zinc status
with zinc supplementation
lowers measures of iron
status in the presence of
low iron reserves (22) and
ii) treatment of iron
deficiency in goitrous
children improves the
efficacy of iodized oil in
reducing goiter (23). Again,
the message is that
trace-element interactions
are most important to
recognize and that they too
determine the phenotype.
Furthermore, although
mild-moderate zinc
deficiency is associated
with symptoms such as poor
appetite, impaired taste and
smell, and poor growth, they
are nonspecific and as Black
and Miguel (24) state "...it
is challenging to identify
zinc deficiency with
certainty." This could
equally be said of most, if
not all, of the other trace
elements. Indeed, some major
questions remain difficult
to answer in this context,
including: i) What is (or
becomes) zinc or any other
trace element deficiency?
ii) What does zinc or other
trace metal balance mean
functionally? iii) How does
the macromolecular state of
cells and organs relate to
the metabolic flux of the
trace element? iv) What are
the time lines involved?
Obviously a zinc, copper or
molybdenum deficiency
doesn't necessarily occur
within a day of inadequate
intake or of increased
losses. These are
deceptively complex issues
that require an answer if
diets are to be optimized
with respect to trace
element content and balance.
Additionally, in terms of
deficiencies we need to ask,
for example, which of the
multiple functions of zinc
(e.g., 25) and/or mechanisms
that account for the
essentiality of zinc in the
animal organism are more or
less vulnerable to a change
in the availability of this
element. i) Is there an
initial and well-defined
acceleration of one or more
apoptotic pathways (a group
of genetically encoded cell
death programs) (26, 27) in
cells, such as precursor
lymphocytes that can be
obtained relatively easily
for evaluation? ii) Is the
formation and /or activity
of one or many of the
zinc-finger proteins (28) or
of the 700+ genes (29) that
encode these transcription
factors affected early on in
the development of the
depletion of zinc pools; or
iii) is DNA repair and
replication (30) more
immediately and profoundly
altered and could this
effect be detected and
localized at the single cell
level by new and modified
comet assays (31)?
As already mentioned, the
challenges here are even
more interesting, as well as
complex, when the
interaction among trace
elements and other nutrients
is duly considered. To
further emphasize: a) the
activity of the DNA binding
domain of the retinoic acid
receptor (containing two
zinc fingers) is diminished
in a pro-oxidant environment
with release of zinc from
the zinc-finger motif (32).
Specifically, does the zinc
deficient phenotype differ
under varying degrees of
antioxidant nutrient status?
b) There is a zinc "sensing"
receptor involved in
intracellular calcium
mobilization and signaling
(33, 34), and c)
mobilization of calcium
induces nitric oxide, which
releases zinc from
metallothionein (35). Hence,
an early biochemical defect
in zinc deficiency might be
a defect in Ca channels, as
the work of O'Dell and
colleagues seems to suggest
(36). The important point,
once again, is that there is
a great deal of cross talk
among and interactions
between trace elements,
other minerals and
nutrients. These have major
ramifications for the way by
which we might widen and
improve approaches for
assessment of trace element
nutritional status and
needs, especially in humans.
Requirements for trace
elements. The foregoing
leads us now briefly to the
second entry on the list in
Table 1, namely the
determination of the
requirements for trace
elements by humans at
different stages of life and
under various physiological,
dietary and environmental
conditions. I think it would
be agreed that, to date, the
approaches used to determine
requirements for trace
elements (37), such as those
indicated in Table 2, are
far from ideal and in some
cases quite unsatisfactory.
Apart from a lack of
information and difficulty
in conducting human studies,
a reason for this problem is
that there has not been a
concerted major research
commitment to establish
requirements for nutrients
in initially healthy humans.
Insufficient resources and a
minimal commitment to
improve upon prior estimates
of requirements contribute
to the current lack of sound
quantitative nutrient
requirement information,
despite its critical
importance for the planning
and evaluation (38) of
diets. As David Baker (39)
said some time ago
"Nutrition scientists often
avoid projects entailing
determination of nutrient
requirements. These studies
are generally considered
routine, easy and lacking in
creativity. Hence, peer
review generally results in
"low marks" for such
endeavors, resulting in
difficulty in obtaining
outside funding." Although
there is considerable truth
to this view, I believe
basic investigators and
those with a more applied
focus in the trace element
arena should coalesce and
integrate some of their
research interests and
efforts in and around the
issue of defining trace
element requirements and
improving assessment of
nutritional status in
quantitative and more
precise predictive terms.
This would lead to
significant and meaningful
advances in trace element
nutrition. Furthermore, it
might also be time for those
of us interested in this
area to step back for a
while and abandon immediate
attempts to refine, for
example, current values for
the mean requirements in
healthy adults for copper
and molybdenum, which are
700 and 34 mg/d,
respectively (37). Rather,
it might now be more
productive to begin
collaborative studies
designed to generate more
complete mechanistically
based information on the
response (pattern of gene
expression, activity of
metabolic pathways,
physiological system
functions, such as those
related to immune and stress
resistance, trace element
kinetics, for example) to
different intake levels of a
specific trace element
within a given
genotype/environmental
context. The lack of good
dose response biological
data characterizes so much
of the knowledge base of
human nutrient requirements.
This might be extremely
difficult to achieve in any
comprehensive way, but I
don't see a major
alternative or otherwise
simple way forward. Such an
effort would, furthermore,
bring into sharper focus and
contact a great deal of
basic biology with the more
applied research findings
and this would measurably
enhance knowledge on
nutritional aspects of trace
elements in man and animals.
With this new knowledge a
better understanding of the
mechanistic basis for and
extent of variation in
requirements among otherwise
apparently similar
individuals would emerge.
The variation in iron
absorption, which accounts
for a major portion of the
difference in iron
requirements among men and
nonmenstruating women, might
have a genetic origin and
perhaps due, at least in
part, to a specific gene
that encodes duodenal
cytochrome B (40), as I have
speculated before (41). The
real point is that a
combination of
genetic/cellular studies
together with whole body
investigations of iron
uptake and dynamics would be
both valuable and exciting
and they would also test the
validity of such an
integrated research
framework. |
Article Source: |
http://jn.nutrition.org/cgi/content/full/133/5/1581S |
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|
Trace Element Analysis
in Biological Specimens |
Edited By
R.F.M. Herber, University of
Amsterdam, Amsterdam, The
Netherlands
M. Stoeppler, Institute of
Applied Physical Chemistry,
Jülich, Germany
The major theme of this book
is analytical approaches to
trace metal and speciation
analysis in biological
specimens. The emphasis is
on the reliable
determination of a number of
toxicologically and
environmentally important
metals. It is essentially a
handbook based on the
practical experience of each
individual author. The scope
ranges from sampling and
sample preparation to the
application of various
modern and well-documented
methods, including quality
assessment and control and
statistical treatment of
data. Practical advice on
avoiding sample
contamination is included.
In the first part, the
reader is offered an
introduction into the basic
principles and methods,
starting with sampling,
sample storage and sample
treatment, with the emphasis
on sample decomposition.
This is followed by a
description of the potential
of atomic absorption
spectrometry, atomic
emission spectrometry,
voltammetry, neutron
activation analysis, isotope
dilution analysis, and the
possibilities for metal
speciation in biological
specimens. Quality control
and all approaches to
achieve reliable data are
treated in chapters about
interlaboratory and
intralaboratory surveys and
reference methods, reference
materials and statistics and
data evaluation.
The chapters of the second
part provide detailed
information on the analysis
of thirteen trace metals in
the most important
biological specimens. The
following metals are treated
in great detail: Aluminium,
arsenic, cadmium, chromium,
copper, lead, selenium,
manganese, nickel, mercury,
thallium, vanadium and zinc.
The book will serve as a
valuable aid for practical
analysis in biomedical
laboratories and for
researchers involved with
trace metal and species
analysis in clinical,
biochemical and
environmental research. |
Article Source: |
http://www.elsevier.com/wps/find/bookdescription.cws_home/524504/description#description |
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|
Trace Element Analysis
of Food and Diet |
Trace element analysis
has a key role to play in
quality control of food and
diet. This timely book
introduces the subject in a
practical way - from
sampling and the techniques
available for trace
analysis, to procedures for
specific elements and data
analysis.
Beginning with a brief
introduction and discussion
of statistical evaluation of
data, the subsequent chapter
looks at trace analysis in
general, with its essentials
and terminology. Another
section introduces sampling
and preparation of
foodstuffs such as wheat,
potato, vegetables and milk.
This is followed by
descriptions of the various
spectrometric techniques
(atomic absorption, atomic
emission, atomic
fluorescence) that are
available. Plasma techniques
for both optical emission
and mass spectrometry are
presented, as are nuclear
activation analysis and
X-ray methods. A comparison
of the various analytical
techniques is provided, and
a separate chapter handles
speciation analysis.
Finally, procedures for
determining essential and
toxic elements such as
arsenic, iron, selenium and
zinc are suggested, using
several recent references.
Detailed explanations and a
simple format will appeal to
laboratory technicians and
graduate students, as well
as more experienced
researchers. Comprehensive
coverage, coupled with
illustrations and a guide to
relevant literature and
manufacturers, will make
Trace Element Analysis of
Food and Diet a valuable
source of information for
anyone working on analysis
of trace elements in food,
diet or other biological or
environmental samples -
particularly food engineers,
agricultural scientists and
government testing agency
employees. |
Article Source: |
http://www.rsc.org/shop/books/2006/9780854045761.asp |
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|
Trace elements in human
body fluids and tissues |
Published figures for
trace element concentrations
in body fluids and tissues
of apparently healthy
subjects are widely
divergent. For a
considerable time, the
apparent disparities were
readily ascribed to
biological sources of
variation such as age, sex,
dietary habits,
physiological conditions,
environmental exposure,
geographical circumstances,
or similar influences.
Growing evidence, however,
suggests that this
interpretation may be
seriously questioned in
numerous instances. First,
values obtained in reference
materials leave no doubt
that some previous studies
must have been subject to
gross analytical
inaccuracies. Second, it has
now been thoroughly
documented that inadequate
sample collection and
manipulation may drastically
distort the intrinsic trace
element content of
biological matrices. This
review scrutinizes data
reported by a number of
investigators. In an effort
to settle the currently
flourishing confusion,
critically selected
reference values are set
forth for trace element
levels in human blood plasma
or serum, packed blood
cells, urine, lung, liver,
kidney, and skeletal muscle
tissue. |
Article Source: |
http://www.ncbi.nlm.nih.gov/pubmed/3891229 |
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|
The human body is
composed of what trace
elements? |
The human body, and
almost all living organisms
are composed primarily or
oxygen (O), carbon (C),
hydrogen, (H), and nitrogen
(N) (listed in order of
decreasing amount).
However, there are many many
other elements present in
our bodies in lower amounts
that are essential for life,
include: sodium (Na),
potassium (K), calcium (Ca),
magnesium (Mg), phosphorus
(P), sulfur (S), chlorine (Cl),
iron (Fe), zinc (Zn), and
many many more trace
elements. The trace elements
are: Li, Be, B, F, Al, Si,
Cl, V, Cr, Mn, Co, Ni, Cu,
As, Se, Br, Rb, Sr, Zr, Mo,
Cd, Sn, I, Cs, Ba, Au, Pb.
Use the WebElements.com link
on the left to see charts of
the periodic table
indicating the abundance of
each element in our body.
There are many ways to view
the data, with interactive
periodic table, charts,
plots, etc. Explore the
different links on the left
side of the linked page.
Make sure to note the
different between the
"logarithmic data" and the
"non-logarithmic data." It
makes a big difference!
That's oxygen, carbon,
hydrogen, Nitrogen, calcium,
phosphorus, potassium,
sulfur, sodium, chlorine,
magnesium, iron, zinc!! |
Article Source: |
http://wiki.answers.com/Q/The_human_body_is_composed_of_what_elements |
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|
Trace-element
analysis defenition |
Trace metal (element)
analysis is utilized in a
wide range of applications,
including medical
diagnostics, medical and
biological research, medical
device implantation clinical
trials, pharmaceutical
analysis, contamination of
food and drinking water,
food/supplement content
analysis and nutritional
evaluation. Trace metals can
be detected in biological
samples; such as blood or
urine, foods and food
supplements,
pharmaceuticals, chemical
compounds, metal alloys,
potable water, along with
several other matrices.
KS employees Inductively
Coupled Plasma Mass
Spectrometry (ICP MS) and
Atomic Absorption (AA)
instrumentation to perform
trace metal analysis on
samples such as those listed
above. Highly sensitive,
quantitative and
semi-quantitative results
can be achieved, to the
parts per billion (ppb)
detection limit.
As a CLIA-certified
laboratory, KSL has
validated assays for
eighteen trace metals in
serum. These trace metals
are; aluminum, antimony,
arsenic, beryllium, cadmium,
chromium, cobalt, copper,
lead, manganese, mercury,
molybdenum, nickel,
selenium, strontium,
thallium, tin and zinc.
Validated assays for are
available on urine, with to
be added in the the near
future.
KS is currently developing
assays for platinum,
titanium and palladium to be
used on a research or
non-human analysis. Most
elements can be detected
using the ICP MS instrument.
For non-human samples, any
trace metal can be detected
in a wide range of specimens
from various matrices.
Element/Metal |
Symbol |
Description |
Aluminum |
Al |
Aluminum
is a metallic
element that has the
atomic number 13,
atomic symbol Al,
and atomic weight
26.98.
|
Antimony |
Sb |
Antimony
is a metallic
element that has the
atomic symbol Sb,
atomic number 51,
and atomic weight
121.75. It is used
as a metal alloy and
as medicinal and
poisonous salts. It
is toxic and an
irritant to the skin
and the mucous
membranes. |
Arsenic |
As |
Arsenic
is a shiny gray
element with atomic
symbol As, atomic
number 33, and
atomic weight 75. It
occurs throughout
the universe, mostly
in the form of
metallic arsenides.
Most forms are
toxic. According to
the Fourth Annual
Report on
Carcinogens (NTP
85-002, 1985),
arsenic and certain
arsenic compounds
have been listed as
known carcinogens |
Beryllium |
Be |
Beryllium
is an element with
the atomic symbol
Be, atomic number 4,
and atomic weight
9.01218. Short
exposure to this
element can lead to
a type of poisoning
known as berylliosis. |
Cadmium |
Cd |
Cadmium
is an element with
atomic symbol Cd,
atomic number 48,
and atomic weight
114. It is a metal
and ingestion will
lead to cadmium
poisioning. |
Chromium |
Cr |
Chromium
is a trace element
that plays a role in
glucose metabolism.
It has the atomic
symbol Cr, atomic
number 24, and
atomic weight 52 |
Cobalt |
Co |
Cobalt
is a trace element
that is a component
of vitamin B12. It
has the atomic
symbol Co, atomic
number 27, and
atomic weight 58.93.
It is used in alloys
and pigments.
Deficiency in
animals leads to
anemia; its excess
in humans can lead
to erythrocytosis. |
Copper |
Cu |
Cooper
is a heavy metal
trace element with
the atomic symbol
Cu, atomic number
29, and atomic
weight 63.55. |
Lead |
Pb |
Lead
is a soft, grayish
metal with poisonous
salts; atomic number
82, atomic weight
207.19, symbol Pb |
Manganese |
Mn |
Manganese
is a trace element
with atomic symbol
Mn, atomic number
25, and atomic
weight 54.94. It is
concentrated in cell
mitochondria, mostly
in the pituitary
gland, liver,
pancreas, kidney,
and bone, influences
the synthesis of
mucopolysaccharides,
stimulates hepatic
synthesis of
cholesterol and
fatty acids, and is
a cofactor in many
enzymes, including
arginase and
alkaline phosphatase
in the liver |
Mercury |
Hg |
Mercury
is a silver metallic
element that exists
as a liquid at room
temperature. It has
the atomic symbol Hg
(from hydrargyrum,
liquid silver),
atomic number 80,
and atomic weight
200.59. Mercury is
used in many
industrial
applications and its
salts have been
employed
therapeutically as
purgatives,
antisyphilitics,
disinfectants, and
astringents. It can
be absorbed through
the skin and mucous
membranes which
leads to MERCURY
POISONING. |
Molybdenum |
Mo |
Molybdenum
is a metallic
element with the
atomic symbol Mo,
atomic number 42,
and atomic weight
95.94. It is an
essential trace
element, being a
component of the
enzymes xanthine
oxidase, aldehyde
oxidase, and nitrate
reductase |
Nickel |
Ni |
Nickel
is a trace element
with the atomic
symbol Ni, atomic
number 28, and
atomic weight 58.69.
It is a cofactor of
the enzyme urease. |
Selenium |
Se |
Selenium
is an element with
the atomic symbol
Se, atomic number
34, and atomic
weight 78.96. It is
an essential
micronutrient for
mammals and other
animals but is toxic
in large amounts.
Selenium protects
intracellular
structures against
oxidative damage. It
is an essential
component of
glutathione
peroxidase. |
Strontium |
Sr |
Strontium
is an element of the
alkaline earth
family of metals. It
has the atomic
symbol Sr, atomic
number 38, and
atomic weight 87.62. |
Thallium |
Tl |
Thallium
is a heavy, soft,
bluish white metal,
atomic number 81,
atomic weight
204.37, symbol Tl |
Tin |
Sn |
Tin
is a trace element
that is required in
bone formation. It
has the atomic
symbol Sn, atomic
number 50, and
atomic weight
118.71. |
Zinc |
Zn |
Zinc
is a metallic
element of atomic
number 30 and atomic
weight 65.38. It is
a necessary trace
element in the diet,
forming an essential
part of many
enzymes, and playing
an important role in
protein synthesis
and in cell
division. Zinc
deficiency is
associated with
anemia, short
stature,
hypogonadism,
impaired wound
healing, and
geophagia. It is
known by the symbol
Zn. |
|
Article Source: |
http://www.kronoslaboratory.com/dotnetnuke/KronosPanels/TraceMetals/tabid/76/Default.aspx |
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