Title of Invention

"SYSTEM AND METHOD FOR EXTRACTING HEADSPACE VAPOR"

Abstract A system and ra&thod for extracting headspace vapor is generally disclosed comprising pressurizing a vessel containing headspace vapor with a carder gas and subsequently venting the sample mixture through an adsorbent trap and out a venl A flow controller is employed to gradually regulate the flow therethrough as the pressure drops as a rcaull of the gradual depletion af headspace vapor in ihc vessel and, in certain embodiments, the flow controller maintains a constant flow ralc, Dae to the time saved. in some embodiments, multiple pressurization-venting cycles. are implemented to maximize tiue amount of vapor extracted from the Vial. Due to the constant flow rate, in certain embodiments, the pressure decey ii monitered and compared to reference values in order to determine whether the sample vessel has a jeak or other defect.
Full Text The Invention
The present invention relates to a system and method for extracting
headspace vapor from a vessel. More specifically, the invention relates to a
system and method for maximizing the amount of vapor extracted by maintaining
5a constant flow as the pressure inside the vessel decreases.
Background Of The Invention
Chromatography is essentially a physical method of separation in which
constituents of a test sample in a carrier gas or liquid are adsorbed or absorbed
and then desorbed by a stationary phase material in a column. A pulse of the
sample is introduced into a steady flow of carrier gas, which carries the sample
lOinto a chromatographic column. The inside of the column is lined with a liquid,
and interactions between this liquid and the various elements of the sample—
which differ based upon differences among distribution coefficients of the
elements—cause the sample to be separated into the respective elements. At
the end of the column, the individual components are more or less separated in
15time. Detection of the gas provides a time-scaled pattern, typically called a
chromatogram, that, by calibration or comparison with known samples, indicates
the constituents of the test sample. An example of the process by which this
occurs is described in U.S. Pat. No. 5,545,252 to Hinshaw.
Often, the sample is first obtained using a sampling device, which
20subsequently transfers the sample to the chromatograph. One means of
obtaining a sample and introducing it into a chromatographic column is known as
"headspace sampling." In conventional headspace sampling, sample material is
sealed in a vial and subjected to constant temperature conditions for a specified
time. Analyte concentrations in the vial gas phase should reach equilibrium with
25the liquid and/or solid phases during this thermostatting time. The vial is
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subsequently pressurized with carrier gas to a level greater than the "natural"
internal pressure resulting from thermostatting and equilibration. Then the
pressurized vial is connected to the chromatographic column in such a way as to
allow for the transfer of a portion of the vial gas phase into the column for a short
period of time. An example of such a sampling device is disclosed in U.S.
Patent No. 4,484,483 to Riegger et. al. An example of a chromatographic
system employing such a sampling device is disclosed in U.S. Patent No.
5,711,786 to Hinshaw, which describes using a chromatographic injector
between the vial and the chromatographic column.
10 Typically, it is desired to pre-concentrate the analytes in the sample, and
occasionally, remove moisture therefrom, prior to introducing the sample into the
chromatographic column. Accordingly, as disclosed in U.S. Patent Nos.
5,792,423 and 6,395,560 to Markelov, these systems will typically include some
kind of "trap" for this purpose, which retains the analytes as they are carried
15through the trap, and which are later released from the trap, usually by heating,
and swept into the chromatographic column.
Though various types of traps have been suggested, one particularly
advantageous way to perform this pre-concentration (and possible moisture
removal) prior to introducing the sample into a chromatographic column is
20through the use of an adsorbent trap. These traps, which adsorb the analytes
and then subsequently desorbed those analytes, do not suffer from the same
slow flow rates as on-line traps (such as cryogenic traps) that result from the
impedance of the column. When using an adsorbent trap, a carrier gas can be
used to first pressurize the vial and then, after pressurization, to carry the sample
25vapor through the trap, which will adsorb the analytes to be measured, and then
vent out of the system, which is the simplest way to extract vapor from a vessel.
Accordingly, numerous arrangements employing an adsorbent trap have been
employed for the purpose of pre-concentrating the analytes of a sample
extracted by a sampling device such as a headspace sampler. Examples of
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such arrangements are disclosed in U.S. Patent No. 5,932,482 to Markelov and
U.S. Patent No. 6,652,625 to Tipler.
However, these systems typically suffer from several disadvantages. One
problem is that the process is slow. This is due to the fact that the pressure in
5the vial is proportional to the amount of sample in the vial. Therefore, as the
sample vapor elutes from the vial, the pressure drops. Accordingly, the rate of
flow decreases, resulting in undesirable vent times. Indeed, trials have shown
that a 22ml_ vial pressurized to 40 psig with helium can take longer than five
minutes to effect a full extraction, even with high initial flow rates.
10 Another problem with current systems is that, in order to maximize
performance with respect to resolution, sensitivity and inertness, it is generally
desired to use capillary columns for chromatography. However, with capillary
columns, the carrier gas flow rates will be low, so direct injection of large
quantities of vapor is not possible. For example, an injection volume of about
15100 uL is typical. A typical headspace sample vial, however, usually has a
capacity of about 22 ml_, with a maximum sample volume about half that.
Therefore, only about 1% of the total headspace vapor is actually injected into
the column. Accordingly, system sensitivity can be increased nearly 100x over
current headspace sampling systems by increasing the percentage of the
20available headspace vapor that is actually injected into the column. This is
particularly useful for applications requiring very low detection limits, such as
environmental and other trace-level analysis of Volatile Organic Compounds
(VOCs) in a variety of sample matrices.
Yet another problem with current systems is that a headspace sampler is
25typically used to test a number of large number vials in sequence, and
occasionally, a vial may have a leak or for some other reason may not contain
the proper amount of sample, leading to erroneous analytical data. Accordingly,
it is advantageous to review the pressure decay profiles for these vials—i.e. in
the decay in pressure as a function of time. However, as previously mentioned,
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the pressure in the vial is proportional to the amount of sample present, and
thus, a plot of pressure decay as a function of time results in exponential, rather
than linear, profiles, making a determination of whether the rate of decay is
appropriate difficult.
5 What is desired, therefore, is a system and method for extracting
headspace vapor that reduces the time required to vent fluid through a trap.
What is further desired is a system and method for extracting headspace vapor
that increases the amount of sample vapor that is actually injected into a
chromatographic column. What is also desired is a system and method for
lOextracting headspace vapor that increases the ability to check for leaks in the
sample vials and verify that the proper amount of sample is present therein.
Summary Of The Invention
Accordingly, an object of the present invention is to provide a system and
method for extracting headspace vapor that prevents the rate of flow through a
trap from decreasing as the sample elutes from a headspace vial.
15 It is a further object of the present invention to provide a system and
method for extracting headspace vapor that effectively extracts residual sample
vapor remaining in the vial after an initial extraction.
It is yet another object of the present invention to provide a system and
method for extracting headspace vapor that produces linear pressure decay
20profiles to facilitate checking for leaks in headspace vials and the presence of
proper sample amounts.
To overcome the deficiencies of the prior art and to achieve at least some
of the objects and advantages listed, the invention comprises a method of
extracting headspace vapor, including providing a vessel holding headspace
25vapor containing analytes to be measured, inserting a receptacle into the vessel,
pressurizing the vessel by communicating carrier gas from a carrier gas inlet
through the receptacle and into the vessel, venting the headspace vapor and
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15
carrier gas in the vessel through an adsorbent, which adsorbs analytes in the
headspace vapor, and out a vent, and controlling the flow of the carrier gas
carrying the headspace vapor as it is vented such that the rate of flow is
increased as the rate of flow decreases due to the depletion of headspace vapor
5in the vessel.
In some of these embodiments, the invention comprises a method for
extracting headspace vapor including repeating the steps of pressurizing and
venting a predetermined number of times.
In certain embodiments, the invention comprises a method for extracting
lOheadspace vapor including monitoring the pressure in the vessel as headspace
vapor is vented from the system.
In another embodiment, the invention comprises a system for extracting
headspace vapor, including a vessel for holding headspace vapor containing
analytes to be measured, a receptacle adapted to be inserted and withdrawn
15from the vessel, the receptacle having a vessel port, a carrier gas inlet for
supplying carrier gas to pressurize the vessel and to carry the headspace vapor,
an adsorbent housing in fluid communication with the carrier gas inlet, the
adsorbent housing having an adsorbent disposed therein for adsorbing the
analytes in the carrier gas carrying the headspace vapor, a vent in fluid
20communication with the adsorbent housing for venting the carrier gas carrying
the headspace vapor, wherein, when the vessel port of the receptacle is in fluid
communication with the vessel and the carrier gas inlet is open, carrier gas flows
into and pressurizes the vessel, wherein, when the vessel port of the receptacle
is in fluid communication with the vessel and the carrier gas inlet is closed, the
25headspace vapor and carrier gas flow into the adsorbent housing and are vented
through the vent, and a flow controller in fluid communication with the adsorbent
housing and the vent for increasing the rate of flow of the carrier gas carrying the
headspace vapor as the rate of flow decreases due to depletion of the
headspace vapor in the vessel.
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20
In some of these embodiments, the invention comprises a system for
extracting headspace vapor including processor for receiving data and
generating a signal causing the steps of pressurizing and venting to be
performed multiple times.
5 In certain embodiments, the invention comprises a system for extracting
headspace vapor including a gauge for monitoring the pressure in the vessel as
headspace vapor is vented from the system.
Brief Description Of The Drawings
Figure 1 is a schematic view of a system for extracting headspace vapor
in accordance with invention in standby mode.
10 Figure 2 is a schematic view of the system for extracting headspace vapor
of Figure 1 during the vial pressurization stage.
Figure 3 is a schematic view of the system for extracting headspace vapor
of Figure 1 during the venting (trap load) stage.
Figure 4 is a schematic view of the system for extracting headspace vapor
15of Figure 1 during the needle withdrawal stage.
Figure 5 is a schematic view of the system for extracting headspace vapor
of Figure 1 during the trap purge stage.
Figure 6 is a schematic view of the system for extracting headspace vapor
of Figure 1 during the trap desorption stage.
20 Figure 7 is a plot of the pressure inside a headspace vial over time.
Detailed Description Of The Drawings
The basic components of one embodiment of a system for extracting
headspace vapor 10 in accordance with the invention are illustrated in Figure 1.
As used in the description, the terms "top," "bottom," "above," "below," "over,"
"under," "on top," "underneath," "up," "down," "upper," "lower," "front," "rear,"
25"forward" and "back" refer to the objects referenced when in the orientation
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illustrated in the drawings, which orientation is not necessary for achieving the
objects of the invention.
As illustrated in Figure 1, which shows the system 10 in standby mode, a
sampling device, such as a headspace sampler, holds a plurality of vessels (i.e.,
headspace vials) 20 that contain the sample to be extracted and analyzed.
Typically, the headspace sampler includes a sampling needle 22 disposed in a
sampling head 24, and the needle 22 is adapted to be inserted and withdrawn
from the vessels 20. The sampling head 24 has a sample chamber 26, and the
sampling needle 22 has a vessel port 28 through which fluid is communicated
lObetween the needle 22 and the interior of the vials 20 and a sample chamber
port 30 through which fluid is communicated between the needle 22 the sample
chamber 26.
An adsorbent housing 32 having an adsorbent 34 disposed therein
(commonly referred to as an adsorbent trap), a flow controller 72, a fixed
15restrictor 74, and a vent 36 are in fluid communication with the sample chamber
26. Accordingly, when headspace vapor is extracted from a vial 20 and mixes
with a carrier gas, this sample mixture can flow through the adsorbent 34, which
will adsorb the analytes to be measured, and out the vent 36 to the atmosphere.
In certain advantageous embodiments, the adsorbent 34 is hydrophobic, thereby
20allowing moisture to be easily purged from the system by carrier gas, as further
explained below. The adsorbent 34 may include any material suitable for this
purpose, such as, for example, graphitized carbon black, a polymeric adsorbent,
or a carbon molecular sieve.
The adsorbent housing 32 is in fluid communication with a gas
25chromatograph, the basic components of which are a chromatographic column
36 and a detector (not shown). Accordingly, analytes that have been adsorbed
by the adsorbent 34 can be desorbed into the column 36. For this reason, in
certain advantageous embodiments, the adsorbent housing 32 is temperature
controllable, and thus, the adsorbent 34 can be heated to desorb the analytes
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retained by the adsorbent 34 before a carrier gas sweeps them out of the
housing 32 and into the column 36.
A plurality of gas inlets are provided to supply and control fluid flowing
throughout the system 10. For example, the system includes a first carrier gas
5inlet 42 for generally providing carrier gas needed by the system. For instance,
the inlet 42 may provide carrier gas to different parts of the system 10 at different
stages of operation, such as, for example, by providing the sampling head 24
with fluid to pressurize the vessel 20, or, as another example, by providing carrier
gas to the adsorbent housing 32 to carry a sample containing analytes thereto or
lOto sweep away moisture contained therein. The system 10 also has a second
gas inlet 44 for providing gas that may be used by various parts of the system at
various stages, but primarily for isolating the chromatographic column 36 from
the rest of the system in order to prevent contaminated fluid from entering the
column 36 until it is specifically desired to desorb the analytes thereinto. The
15system also includes a third inlet 46, primarily for providing carrier gas to the
adsorbent housing 32 in order to sweep analytes into the column 36 as the
analytes are desorbed from the adsorbent 34. Valves 52, 54, 56 are provided to
open and close inlets 42, 44, 46, respectively.
Operation of the above described assembly is illustrated stepwise Figures
202-7. A pressurization step is illustrated in Figure 2. As shown therein, the
sampling needle 22 descends into the vial 20, bringing the vessel port 28 into
fluid communication with the interior of the vial 20. The inlets 42, 44, 46 are all
opened, sending fluid into the sample chamber 26, through the chamber port 30,
down through the needle 22, and into the vial 20 (indicated by arrows A). In this
25way, the vial is pressurized.
A venting (or trap load) step is illustrated in Figure 3. As shown therein,
the inlet valve 52 is closed, terminating the supply of fluid from the inlet 42.
Likewise, the valve 56 terminates the supply of fluid from inlet 46. As a result,
fluid containing the analytes to be measured elutes from the vial 20 through the
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vessel port 28, through the needle 22, out the chamber port 30, through the
adsorbent housing 32, where the adsorbent 34 adsorbs the analytes, and out
through the vent 36. (indicated by arrows B). The inlet valve 54 remains open,
allowing fluid to continue to enter through the inlet 44 and isolate the column 36
5(indicated by arrows C).
Because the pressure in the vial 20 is proportional to the amount of
sample in the vial 20, the pressure drops as the headspace vapor elutes from
the vial 20, which normally causes the rate of flow to gradually decrease during
the venting process. To counter this result, the flow controller 72, in response to
lOthe gradual decrease in pressure, gradually increases the flow therethrough,
effectively increasing the rate of flow as the depletion of the headspace vapor in
the vial 20 decreases the rate of flow. In certain advantageous embodiments,
the flow controller 72 is configured to increase flow in an amount directly
proportional to the decrease in pressure, thereby maintaining a constant flow
15rate. In this way, the process of extracting headspace vapor from the vial 20
does not immediately begin gradually slowing down as the venting stage
proceeds, thereby resulting in quicker extraction times.
In some embodiments, the flow controller 72 comprises a forward
pressure regulator. However, in other embodiments, the flow controller may
20comprises any device suitable for controlling flow therethrough, such as, for
example, a mass flow controller or an electronic flow controller.
The aforementioned steps of pressurizing the sample vial 20 and venting
the headspace therein through the adsorbent housing 32 and out the vent 36,
however, does not extract all of the headspace from the vial 20. Instead, a
25certain percentage of the original headspace vapor remains in the vial 20 at
atmospheric pressure. This residual vapor remaining in the vial 20 after the
initial pressurization and venting is represented by the following equation:
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where R is the residual vapor (percentage of original headspace vapor)
remaining in the vial, P,o is the absolute pressure (normally, atmospheric) after
venting through the adsorbent housing 32 has occurred, and Phi\s the absolute
5pressure (elevated) before venting through the adsorbent housing 32 has
occurred.
While increasing the value of Phi or reducing the value of P/o would
increase the amount of vapor extracted, a more practical way of reducing the
value of R (i.e., increasing the amount of vapor extracted) is by performing
multiple pressurization/venting cycles. Because the amount of time expended to
perform a pressurization-venting cycle is significantly decreased due to the use
of the flow controller 72 to maintain a constant flow rate, it is possible to perform
multiple cycles in succession. When multiple cycles are performed, the residual
vapor is represented by the equation:

where n is the number of cycles. As is readily seen, the lower the pressure, the
more pressurization-venting cycles are required in order to reduce the value of R
(i.e., increase the amount of vapor extracted) to a particular desired value.
Typically a processor 70 automatically controls the amount of
20pressurization-venting cycles that are performed. Accordingly, an operator of the
system 10 can determine how many cycles are desired by deciding upon an
appropriate balance between the amount of vapor to be extracted and the
amount of time to be expended performing additional cycles, and the operator
can then input this value to the processor 70. Alternately, the operator can
25determine what percentage of residual vapor (R) is acceptable and input this
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value to the processor 70, which can then calculate amount of pressurization-
venting cycles required according to the following equation:
The number of pressurization-venting cycles input by the operator, or
5calculated by the processor 70, are then performed successively before the
system 10 proceeds to perform the remaining steps discussed below. Figure 8
illustrates a representation of the pressure inside the vial over time when multiple
pressurization-venting cycles are employed.
Returning again to Figure 3, in certain advantageous embodiments, the
10system 10 includes a gauge for determining the pressure in the headspace vial
20. Though this may be any device capable of measuring the pressure in the
vial 20 and communicating this information to either the system or an operator of
the system, in certain embodiments, this gauge is a pressure transducer 62 in
fluid communication with the vial 20. Accordingly, as the carrier gas carrying the
15headspace vapor flows past the transducer 62, the operator may be promptly
alerted upon detection of an undesirable condition in the vial 20 by, for example,
an LED, an audible alarm, or a log report or profile on a visual display screen.
Because the rate of flow remains constant due to the use of the flow
controller 72, various undesirable conditions can be easily detected by
20monitoring the pressure with the transducer 62, such as a leak in the vial, an
incorrect starting pressure, an defective vial resulting in abnormal vial capacity,
or the presence of too much or too little sample in the vial. As noted above, the
drop in pressure is proportional to the amount of sample flowing out of the vial
20. Because vent time is normally proportional to both the sample volume in the
25vessel and the pressure, a plot of the pressure decay overtime generally results
in an exponential profile, making measurement and comparison of the pressure
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decays somewhat difficult. However, because the flow controller 72 maintains a
constant flow rate, a plot of the pressure decay over time results in a linear
profile. Therefore, measurement of the pressure decay is very useful in
determining whether the vial has a leak or other undesired condition.
5 The system is first calibrated by obtaining a properly measured and
sealed reference vial and running it on the headspace sampler. A number of
readings of the pressure are taken at various points in time and stored in system
memory for later comparison. Later, as each actual sample vial is tested, the
same number of readings are taken and are subsequently compared to the
10corresponding values stored for the reference vial, and will check for any
significant deviation. For example, the system may take twenty one readings for
each of the reference vial and the sample vials, and then look for a deviation in
the values of the sample vials of more than ten percent in three successive
points from the reference vial. Values that are too high, for example, may
indicate that too much sample may be present in the vial, while values that are
too low may indicate that too little sample is in the vial or that the vial has a leak.
If a deviation is found, the sample may be flagged in a system log or the operator
may be otherwise alerted to the defective vial.
The transducer 62 may be located anywhere suitable for measuring the
20pressure prior to the influence of a flow controller. For example, as disclosed in
Figure 3, a transducer 64 may be positioned in the flow path immediately
preceding the flow controller 72. However, in certain advantageous
embodiments, a position proximate to the sampling head 24 is used, such as the
position of pressure transducer 62 located at the needle purge 66, in order to
25avoid possible external factors from effecting an accurate measurement of the
pressure, such as, for example, a slight pressure drop across the adsorbent 34.
Next, in embodiments where a significant amount of moisture is present in
the sample being analyzed, a dry purge step may be desired. As shown in
Figure 4, the needle 22 is first withdrawn from the vial 20, bringing the vessel
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port 28 above the seal 60. Next, as illustrated in Figure 5, the inlet valve 52 is
opened again, thereby allowing fluid to once again enter the system via the inlet
42. The fluid flows down into the adsorbent housing 32, sweeping any moisture
therein out through the vent 36 (indicated by arrows D). Once again, the inlet
5valve 54 remains open, allowing fluid to continue to enter through the inlet 44
and isolate the column 36 (indicated by arrows E).
A desorption step is illustrated in Figure 6. As shown therein, the valves
52, 54 are closed, terminating the supply of fluid from inlets 42, 44. The valve 56
is opened, allowing fluid to flow in through inlet 46. The adsorbent housing 32 is
10heated to desorb the analytes retained by the adsorbent 34. Carrier gas enters
through the inlet 46 and flows into the adsorbent housing 32, sweeping the
desorbed analytes into the chromatographic column 36 (indicated by arrows F).
It should be understood that the foregoing is illustrative and not limiting,
and that obvious modifications may be made by those skilled in the art without
15departing from the spirit of the invention. Accordingly, reference should be made
primarily to the accompanying claims, rather than the foregoing specification, to
determine the scope of the invention.
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What is claimed is:
1. A method of extracting headspace vapor, the method comprising the
steps of:
providing a vessel holding headspace vapor containing analytes to be
5measured;
inserting a receptacle into the vessel;
pressurizing the vessel by communicating carrier gas from a carrier gas
inlet through the receptacle and into the vessel;
venting the headspace vapor and carrier gas in the vessel through an
10adsorbent, which adsorbs analytes in the headspace vapor, and out a vent; and
controlling the flow of the carrier gas carrying the headspace vapor as it is
vented such that the rate of flow is increased as the rate of flow decreases due
to the depletion of headspace vapor in the vessel.
2. A method as claimed in claim 1, wherein the step of venting the
15headspace vapor and carrier gas comprises closing the carrier gas inlet.
3. A method as claimed in claim 1, further comprising the step of desorbing
the analytes adsorbed by the adsorbent.
4. A method as claimed in claim 2, further comprising the step of purging the
adsorbent of moisture by venting additional carrier gas through the adsorbent
20and out the vent prior to the step of desorbing the analytes.
5. A method as claimed in claim 1, wherein the step of controlling the flow
comprises increasing the flow through a flow controller in response to a decrease
in pressure.
6. A method as claimed in claim 1, wherein the step of controlling the flow
25comprises maintaining a constant flow rate by increasing the rate of flow in an
amount equal to the decrease in the rate of flow resulting from depletion of
headspace vapor in the vessel.
7. A method as claimed in claim 1, further comprising repeating the steps of
pressurizing and venting a predetermined number of times.
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8. A method as claimed in claim 7, wherein the steps of pressurizing and
venting comprise a pressurization-venting cycle, the method further comprising
the step of:
determining the total number of pressurization-venting cycles to be
5performed; and
wherein the predetermined number of times the steps of pressurizing and
venting are repeated is one less than the determined total number of
pressurization-venting cycles to be performed.
9. A method as claimed in claim 8, wherein the step of determining the total
10number of pressurization-venting cycles to be performed comprises the steps of:
determining a percentage of the original headspace vapor to remain in the
vessel as residual vapor; and
calculating the number of pressurization-venting cycles required to extract
enough of the original headspace vapor from the vessel such that the
I5percentage of original headspace vapor remaining in the vessel after performing
the calculated number of pressurization-venting cycles does not exceed the
determined percentage.
10. A method as claimed in claim 9, wherein the number of pressurization-
venting cycles required is calculated according to the equation:

11. A method as claimed in claim 1, further comprising the step of monitoring
the pressure in the vessel as the carrier gas carrying the headspace vapor is
vented through the adsorbent and the vent to determine the rate of pressure
decay in the monitored vessel.
2512. A method as claimed in claim 11, further comprising the steps of:
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measuring the rate of pressure decay in a reference vessel to determine
the rate of pressure decay therein;
comparing the rate of pressure decay in the monitored vessel to the rate
of pressure decay in the reference vessel to determine if the monitored vessel is
5defective.
13. A system for extracting headspace vapor, comprising:
a vessel for holding headspace vapor containing analytes to be
measured;
a receptacle adapted to be inserted and withdrawn from said vessel, said
10receptacle having a vessel port;
a carrier gas inlet for supplying carrier gas to pressurize said vessel and to
carry the headspace vapor;
an adsorbent housing in fluid communication with said carrier gas inlet,
said adsorbent housing having an adsorbent disposed therein for adsorbing the
15analytes in the carrier gas carrying the headspace vapor;
a vent in fluid communication with said adsorbent housing for venting the
carrier gas carrying the headspace vapor;
wherein, when the vessel port of said receptacle is in fluid communication
with said vessel and said carrier gas inlet is open, carrier gas flows into and
20pressurizes said vessel;
wherein, when the vessel port of said receptacle is in fluid communication
with said vessel and said carrier gas inlet is closed, the headspace vapor and
carrier gas flow into said adsorbent housing and are vented through said vent;
and
25 a flow controller in fluid communication with said adsorbent housing and
said vent for increasing the rate of flow of the carrier gas carrying the headspace
vapor as the rate of flow decreases due to depletion of the headspace vapor in
said vessel.
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14. A system as claimed in claim 13, wherein said flow controller is configured
to increase the flow therethrough in response to a decrease in pressure.
15. A system as claimed in claim 13, wherein said flow controller is configured
to maintain a constant flow rate by increasing the rate of flow in an amount equal
5to the decrease in the rate of flow resulting from depletion of headspace vapor in
the vessel.
16. A system as claimed in claim 13, wherein said flow controller comprises a
forward pressure regulator.
17. A system as claimed in claim 13, wherein said flow controller comprises a
10mass flow controller.
18. A system as claimed in claim 13, wherein said flow controller comprises
an electronic flow controller.
19. A system as claimed in claim 13, further comprising a processor, wherein:
the pressurization of said vessel and the venting of the headspace vapor
15and carrier gas through said vent comprise a pressurization-venting cycle;
said processor is configured to receive data reflecting a number of
pressurization-venting cycles; and
said processor is configured to generate a signal causing the number of
pressurization-venting cycles to be performed.
2020. A system as claimed in claim 13, further comprising a processor, wherein:
the pressurization of said vessel and the venting of the headspace vapor
and carrier gas through said vent comprise a pressurization-venting cycle;
said processor is configured to receive data reflecting a maximum
percentage of the original headspace vapor in the vessel to remain as residual
25vapor;
said processor is configured to calculate a number of pressurization-
venting cycles required to extract enough headspace vapor from said vessel so
as not to exceed the maximum percentage; and
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said processor is configured to generate a signal causing the calculated
number of pressurization-venting cycles to be performed.
21. A system as claimed in claim 20, wherein said processor is configured to
calculate the number of pressurization-venting cycles according to the equation:

22. A system as claimed in claim 13, further comprising a gauge for
monitoring the pressure in said vessel as headspace vapor flows out of said
vessel.
23. A system as claimed in claim 22, wherein said gauge comprises a
10pressure transducer.
23. A method as claimed in claim 22, further comprising a memory for storing
the rate of pressure decay in a reference vessel for later comparison with the
rate of pressure decay in the monitored vessel to determine if the monitored
vessel is defective.
1524. A system as claimed in claim 13, wherein said adsorbent comprises
carbon black.
25. A system as claimed in claim 13, wherein said adsorbent comprises a
polymeric adsorbent.
26. A system as claimed in claim 13, wherein said adsorbent comprises a
20carbon molecular sieve.
Express Mail No. EL 574 206 822 US


A system and ra&thod for extracting
headspace vapor is generally disclosed comprising
pressurizing a vessel containing headspace vapor
with a carder gas and subsequently venting the
sample mixture through an adsorbent trap and out
a venl A flow controller is employed to gradually
regulate the flow therethrough as the pressure drops
as a rcaull of the gradual depletion af headspace
vapor in ihc vessel and, in certain embodiments, the
flow controller maintains a constant flow ralc, Dae
to the time saved. in some embodiments, multiple
pressurization-venting cycles. are implemented
to maximize tiue amount of vapor extracted from
the Vial. Due to the constant flow rate, in certain
embodiments, the pressure decey ii monitered and
compared to reference values in order to determine
whether the sample vessel has a jeak or other defect.

Documents:


Patent Number 218685
Indian Patent Application Number 02016/KOLNP/2005
PG Journal Number 15/2008
Publication Date 11-Apr-2008
Grant Date 09-Apr-2008
Date of Filing 14-Oct-2005
Name of Patentee PERKINELMER LAS, INC.
Applicant Address 549 ALBANY STREET, BOSTON, MA 02118 U.S.A.
Inventors:
# Inventor's Name Inventor's Address
1 TIPLER, ANDREW S3 BROOK SIDE DRIVE, TRUMBULL, CT 06611 U.S.A.
2 MAZZA, CHRISTOPHER 10 GRIFFIN ROAD, TERRYVILLE, CT 06786 U.S.A.
PCT International Classification Number G01N 1/22, 30/08
PCT International Application Number PCT/US2004/011487
PCT International Filing date 2004-04-14
PCT Conventions:
# PCT Application Number Date of Convention Priority Country
1 60/481, 558 2003-10-24 U.S.A.
2 60/462, 731 2003-04-14 U.S.A.