US20120247188A1 - Gas Sample Collection and Analysis - Google Patents
Gas Sample Collection and Analysis Download PDFInfo
- Publication number
- US20120247188A1 US20120247188A1 US13/482,983 US201213482983A US2012247188A1 US 20120247188 A1 US20120247188 A1 US 20120247188A1 US 201213482983 A US201213482983 A US 201213482983A US 2012247188 A1 US2012247188 A1 US 2012247188A1
- Authority
- US
- United States
- Prior art keywords
- sample
- gas
- sample gas
- accumulator
- volume
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
Images
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N1/00—Sampling; Preparing specimens for investigation
- G01N1/02—Devices for withdrawing samples
- G01N1/22—Devices for withdrawing samples in the gaseous state
Definitions
- This invention relates to the field of chemical analysis and more specifically to the field of sample gas collection and analysis.
- Chemical analysis often includes analyzing the amount of carbon or other elements such as nitrogen in a sample.
- Conventional practice for detecting carbon or such other elements in samples employs techniques to convert the element of interest to a gas product prior to making the measurement. For instance, through oxidation or combustion, carbon in the sample may be combined with oxygen to produce carbon dioxide.
- the gas of interest is typically transferred to a calibrated analyzer (i.e., total organic carbon analyzer) by which the gas of interest is measured in a single-pass measurement to determine the level of product present in the sample.
- Drawbacks include the inability to store a sample for later analysis. Additional drawbacks with the single-pass measurement include the inability to satisfy a need for multiple analyses of a sample. Further drawbacks to the single-pass measurement include no opportunity to re-test after adjusting system parameters when calibration ranges are exceeded or detection limits are not achieved.
- NDIR nondispersive infrared sensor
- Drawbacks to current analyzer designs include the limitation of the detector range capability.
- direct measurement systems drive operational inefficiencies involving samples with a high concentration of the product of interest and generate gas concentrations above the calibration or saturation points of the detector. Additional inefficiencies include samples with concentrations of the product of interest that are too low to generate gases or with concentrations above the detection limit of the detector.
- a system for capturing a sample gas for analysis includes an accumulator.
- the accumulator has a variable volume. A volume of the sample gas is fed to the accumulator.
- the system also includes an analyzer. An aliquot of the sample gas is withdrawn from the accumulator and fed to the analyzer. The analyzer analyzes a desired component of the sample gas.
- FIG. 1 illustrates a sample analysis process including an accumulator and a sample collection apparatus
- FIG. 2 illustrates an exploded view of an accumulator having a sample side comprising a flexible bag
- FIG. 3 illustrates a sample analysis process including a sample collection apparatus and an accumulator comprising a flexible bag;
- FIG. 4 illustrates an accumulator
- FIG. 5 illustrates a cross sectional side view of an embodiment of an accumulator in which the accumulator is purged by a purge gas
- FIG. 6 illustrates a cross sectional side view of an embodiment of an accumulator in which a sample is being added to the accumulator
- FIG. 7 illustrates a cross sectional side view of an embodiment of an accumulator in which the accumulator is about full of sample gas.
- FIG. 1 illustrates a sample analysis process 5 that includes accumulator 10 and sample gas collection apparatus 15 .
- Accumulator 10 is a sealed device suitable for allowing the transfer of sample gases at constant pressure.
- accumulator 10 has a sealed chamber 30 that includes a chamber separator 35 or a flexible bag 165 .
- accumulator 10 is a flexible bag 165 .
- Accumulator 10 has a variable volume by which a variable volume of sample gas 105 may be contained. It is to be understood that in FIG. 1 accumulator 10 is illustrated in a cross sectional side view.
- accumulator 10 includes chamber 30 , chamber separator 35 , sample side 40 , and. pressure side 45 .
- Chamber separator 35 is a flexible membrane that separates sample side 40 from pressure side 45 and prevents the flow of any gas between sample side 40 and pressure side 45 .
- Chamber. separator 35 is secured to chamber 30 by any suitable means.
- FIG. 2 illustrates an exploded perspective view of an embodiment of accumulator 10 in which accumulator 10 includes flexible bag 165 .
- flexible bag 165 is attached to sample orifice 20 to allow sample gas 105 to flow in and out of flexible bag 165 .
- Chamber separator 35 and flexible bag 165 are flexible membranes that are impermeable by gas.
- chamber separator 35 and flexible bag 165 are flexible and impermeable by gas but are non-elastic.
- elastic deformation of chamber separator 35 or flexible bag 165 may impart varying pressure on sample gas 105 , and in some embodiments a constant pressure is desired in the operation of accumulator 10 .
- the constant pressure is at atmospheric pressure.
- a constant pressure is desired to eliminate the number of pumping, measuring, and regulating devices involved with pressurized systems.
- Chamber separator 35 and flexible bag 165 may be composed of any material that is flexible but non-elastic.
- chamber separator 35 and flexible bag 165 examples include high density polyethylene or MYLAR, which is a registered trademark of E.I. Du Pont de Nemours and Company.
- chamber separator 35 and flexible bag 165 may have a minimum amount of elasticity.
- chamber separator 35 and flexible bag 165 may be composed of any flexible and non gas permeable materials that exhibit elasticity.
- the materials of chamber separator 35 and flexible bag 165 are selected based on the, chemical nature of the gases involved and compatibility therewith.
- chamber 30 is composed of any materials suitable for supporting chamber separator 35 .
- chamber 30 may be composed of acrylonitrile-butadiene-styrene (ABS), polycarbonate, polymethyl methacrylate (PMMA), aluminum, steel, plastic, or any combination thereof.
- FIG. 4 illustrates a perspective view of accumulator 10 showing chamber 30 having a sample orifice 20 and a purge gas orifice 25 .
- Sample orifice 20 may have any size and configuration suitable for allowing sample gas 105 to be introduced and exit accumulator 10 .
- Purge gas orifice 25 may have any size and configuration suitable for allowing purge gas to be introduced and exit accumulator 10 . It is to be understood that FIG.
- chamber 30 is composed of two portions that are secured to each other by securing means 50 .
- Securing means 50 may include any securing means suitable for securing the two portions to each other, such as screws.
- Chamber 30 is not limited to the configuration and design of FIG. 4 but instead may have any other suitable design and configuration for allowing the transfer of sample gas 105 at constant pressure.
- sample gas collection apparatus 15 may include any method and apparatus for collecting a sample gas from a solid, liquid, or gas sample.
- suitable methods for sample gas collection apparatus 15 include combustion, chemical reaction, catalytic reactions, and the like. Combustion may be accomplished by any suitable method such as by a combustion furnace.
- FIGS. 1 and 3 illustrate embodiments in which sample gas collection apparatus 15 is a combustion furnace for combusting a solid sample 85 .
- the combustion furnace is not limited to the combustion furnace configuration illustrated in FIGS. 1 and 3 but instead may include any configuration for collecting a sample gas.
- gas supply 60 provides a gas 65 to sample gas collection apparatus 15 .
- gas supply 60 is a pressurized gas supply.
- Gas 65 is any combustion gas suitable for use in combustion of sample 85 .
- examples of gas 65 include oxygen, air, and the like.
- gas 65 is fed through a valve 70 and flow restrictor 75 through riser tube, which may control the flow of gas 65 to sample gas collection apparatus 15 .
- Flow restrictor 75 is any flow restrictor such as a sintered metal frit that is suitable for restricting the flow of sample gas collection apparatus 15 .
- sample analysis process 5 does not include valve 70 and/or flow restrictor 75 .
- Gas 65 is fed to sample gas collection apparatus . 15 through riser tube 90 to create an oxygen rich environment inside the furnace in which combustion takes place to combust sample 85 , which is disposed on riser tube 90 .
- Sample gas 105 flows out of sample gas collection apparatus 15 and into sample side 40 of accumulator 10 . In some embodiments, sample gas 105 flows through catalyst in the end of the combustion chamber. Sample gas 105 includes the oxygen from gas 65 and the products of combustion.
- sample gas 105 may be passed through water removal apparatus 110 prior to being fed to accumulator 10 .
- Water removal apparatus 110 may be any device suitable for removing water or any other liquid from sample gas 105 .
- water removal apparatus 110 may be a particulate filter, a condensation trap, or the like.
- accumulator 10 includes chamber separator 35 .
- accumulator 10 operates at atmospheric pressure.
- Accumulator 10 has valve 170 that connects pressure side 45 to vent 120 . Vent 120 is a vent to the atmosphere.
- valve 170 is open to vent 120 , which allows any gas in pressure side 45 to escape accumulator 10 and thereby prevents the increasing volume of sample gas 105 in sample side 40 from resulting in an increased pressure in accumulator 10 .
- sample gas 105 may be fed to accumulator 10 at low pressures.
- sample gas 105 may be corrosive and/or particulate bearing.
- accumulator 10 may be operated at higher than atmospheric pressures. For instance, a backpressure regulator may be added between pressure side 45 and vent 120 to provide a constant, above atmospheric pressure.
- Advantages of higher than atmospheric pressures include allowing larger sample volume to be collected with a much smaller container (i.e., accumulator 10 ).
- FIGS. 5-7 illustrate adding volume of sample gas 105 to an embodiment of accumulator 10 as illustrated in FIG. 1 in which accumulator 10 has chamber separator 35 .
- accumulator 10 is substantially full of gas on pressure side 45 with no sample gas 105 on sample side 40 .
- accumulator 10 has about no volume on sample side 40 .
- FIG. 6 illustrates an embodiment in which a volume of sample gas 105 is being added to accumulator 10 with chamber separator 35 preventing sample gas 105 from flowing to pressure side 45 .
- FIG. 7 illustrates an embodiment in which accumulator 10 is about full of a volume of sample gas 105 with, no sample gas 105 flowing out of accumulator 10 through pressure side 45 .
- valve 115 isolates sample side 40 from sample gas collection apparatus 15 (i.e., the combustion furnace).
- Valve 130 is switched to open accumulator 10 to analyzer 150 , and a measured aliquot is pulled from accumulator 10 to analyzer 150 .
- Analyzer 150 may pull multiple aliquots of the same volume or different volumes of sample gas 105 from accumulator 10 .
- sample gas 105 is stored in accumulator 10 until it is desired for analysis.
- Analyzer 150 may include any analyzer suitable for analyzing a gas sample. Analyzer 150 analyzes a desired component of sample gas 105 .
- the analysis may include determining the amount of a component in sample gas 105 .
- the component may be any desired component such as carbon (i.e., total carbon analysis), nitrogen (i.e., total nitrogen analysis), sulfur, and the like.
- analyzer 150 measures the amount of carbon in sample gas 105 .
- sample side 40 may be purged of sample gas 105 .
- Purging of sample side 40 includes switching valve 130 to open sample side 40 to vent 120 .
- valve 170 is switched to pressurize pressure side 45 , which purges sample side 40 of sample gas 105 .
- FIG. 1 illustrates an embodiment in which pressure side 45 is pressurized by the same gas 65 that is fed to sample gas collection apparatus 15 . In alternative embodiments (not illustrated), pressure side 45 is pressurized by a different gas than gas 65 .
- Pressurization of pressure side 45 purges sample side 40 by increasing the pressure and volume on pressure side 45 , which reduces the volume in sample 40 and forces sample gas 105 out of accumulator 10 and to vent 120 .
- valve 170 is switched back to vent 120 , valve 130 is switched away from vent 120 and closed.
- valve 135 is switched to allow gas 65 (or another purge gas) to flow into sample side 40 for a purge of sample side 40 .
- Valve 135 is then closed to the flow of gas 65 , valve 130 is opened to vent 120 , and valve 170 is opened to allow the flow of gas 65 to fill pressure side 45 and purge sample side 40 of gas 65 .
- a timer controls the amount of sample gas 105 and gas 65 fed to sample side 40 and pressure side 45 during sample analysis process 5 .
- accumulator 10 includes flexible bag 165 disposed in chamber 30 , the same operation steps as described for the above operation of the embodiment of accumulator 10 having sample side 40 and chamber separator 35 apply, with it to be understood that flexible bag 165 operationally takes the place of both the sample side 40 and chamber separator 35 .
- valve 130 is opened to vacuum 160 , and vacuum 160 removes any gas in accumulator 10 .
- valve 130 is closed, and sample gas 105 is fed to accumulator 10 .
- valve 115 is switched to isolate sample gas 105 in accumulator 10 from sample gas collection apparatus 15 (i.e., the combustion furnace).
- Valve 130 is switched to open accumulator 10 to analyzer 150 , and a measured aliquot is pulled from accumulator 10 to analyzer 150 .
- Analyzer 150 may pull multiple aliquots of the same volume or different volumes of sample gas 105 from accumulator 10 .
- sample gas 105 is stored in accumulator 10 until it is desired for analysis.
- accumulator 10 may be purged of sample gas 105 .
- Purging of accumulator 10 includes switching valve 130 to open flexible bag 165 to vacuum 160 , which purges accumulator 10 of sample gas 105 .
- accumulator 10 may then be flushed by the same gas 65 or by a different gas.
- valve 130 is closed, and valve 135 allows gas 65 to feed into accumulator 10 .
- valve 135 closes the flow of gas 65 , and valve 130 is opened to vacuum 160 , which purges accumulator 10 of gas 65 .
- a timer controls the amount of sample gas 105 and gas 65 fed to accumulator 10 during sample analysis process 5 .
- sample analysis process 5 may also include valve 100 , which allows a backflow of gas 65 to prevent combustion tube 80 from being contaminated with atmospheric carbon dioxide.
- gas 65 may flow through a flow restrictor 125 before valve 100 .
- FIGS. 1 and 3 include using flow restrictors 75 , 125 to set timed flow rates for a known amount of gas, but that sample analysis process 5 is not limited to use of such flow restrictors 75 , 125 .
- any other desirable method may be used in combination with or instead of flow restrictors 75 , 125 .
- pressure and temperature sensors, heaters, and flow controllers may be used for precise control and data logging purposes.
- sample analysis process 5 does not include sample gas collection apparatus 15 but instead the desired sample gas 105 to be analyzed is provided and fed to accumulator 10 with sample analysis process 5 operating otherwise as described above.
- chamber separator 35 and flexible bag 165 are elastic.
- sample side 40 and flexible bag 165 are not fully filled with sample 105 , which prevents elastic deformation of chamber separator 35 and flexible bag 165 from sample gas 105 and allows a constant pressure in accumulator 10 .
- sample analysis process 5 including accumulator 10 provides the advantage of regulating the amount of sample gas 105 passed to analyzer 150 . Additional advantages include the ability to store sample gas 105 for analysis at a later time. Further advantages provided include adjusting the size of samples (i.e., the aliquots) fed to analyzer 150 as well as allowing repeated samples of the same size to be fed to analyzer 150 . For instance, in some embodiments, small aliquots of sample gas 105 may be desired for analysis for high carbon content, and large aliquots of sample gas 105 may be desired for low carbon content. Consequently, sample analysis process 5 provides a reservoir (i.e., accumulator 10 ) to provide a broad range of sample sizes for a multitude of measurements.
- a reservoir i.e., accumulator 10
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Biomedical Technology (AREA)
- Molecular Biology (AREA)
- Physics & Mathematics (AREA)
- Chemical & Material Sciences (AREA)
- Analytical Chemistry (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- General Physics & Mathematics (AREA)
- Immunology (AREA)
- Pathology (AREA)
- Sampling And Sample Adjustment (AREA)
Abstract
A system and method for capturing a sample gas for analysis is disclosed. In one embodiment, the system includes an accumulator that has a variable volume. A volume of the sample gas is fed to the accumulator. The system also has an analyzer. An aliquot of the sample gas is withdrawn from the accumulator and fed to the analyzer. The analyzer analyzes a desired component of the sample gas.
Description
- This application is a non-provisional application that claims the benefit of U.S. application Ser. No. 60/917,955 filed on May 15, 2007, which is incorporated by reference herein in its entirety.
- Not applicable.
- 1. Field of the Invention
- This invention relates to the field of chemical analysis and more specifically to the field of sample gas collection and analysis.
- 2. Background of the Invention
- Chemical analysis often includes analyzing the amount of carbon or other elements such as nitrogen in a sample. Conventional practice for detecting carbon or such other elements in samples (i.e., solid, sludge or aqueous samples) employs techniques to convert the element of interest to a gas product prior to making the measurement. For instance, through oxidation or combustion, carbon in the sample may be combined with oxygen to produce carbon dioxide. The gas of interest is typically transferred to a calibrated analyzer (i.e., total organic carbon analyzer) by which the gas of interest is measured in a single-pass measurement to determine the level of product present in the sample. Drawbacks include the inability to store a sample for later analysis. Additional drawbacks with the single-pass measurement include the inability to satisfy a need for multiple analyses of a sample. Further drawbacks to the single-pass measurement include no opportunity to re-test after adjusting system parameters when calibration ranges are exceeded or detection limits are not achieved.
- Conventional analyzers use a variety of oxidation techniques including combustion chemical reactions and catalytic reactions to convert target products to the analytical gas for measurement by the analyzer detection system. For instance, an example of a conventional analyzer detector is a nondispersive infrared sensor (NDIR). Drawbacks to current analyzer designs include the limitation of the detector range capability. In addition, direct measurement systems drive operational inefficiencies involving samples with a high concentration of the product of interest and generate gas concentrations above the calibration or saturation points of the detector. Additional inefficiencies include samples with concentrations of the product of interest that are too low to generate gases or with concentrations above the detection limit of the detector.
- Consequently, there is a need for an improved process for measuring the level of a component in a sample. Further needs include an improved process that allows for multiple measurements to be made on the gases generated from a single sample. Needs also include an improved process that provides analyzer designs to operate over a broader dynamic range and be fault tolerant to over and under ranging.
- These and other needs in the art are addressed in one embodiment by a system for capturing a sample gas for analysis. The system includes an accumulator. The accumulator has a variable volume. A volume of the sample gas is fed to the accumulator. The system also includes an analyzer. An aliquot of the sample gas is withdrawn from the accumulator and fed to the analyzer. The analyzer analyzes a desired component of the sample gas.
- These and other needs in the art are addressed in another embodiment by a method for capturing a sample gas for analysis. The method includes feeding the sample gas to an accumulator, wherein the accumulator has a variable volume. The method also includes withdrawing an aliquot of the sample gas from the accumulator. The method further includes feeding the aliquot of the sample gas to an analyzer. In addition, the method includes analyzing a desired component of the sample gas.
- The foregoing has outlined rather broadly the features and technical advantages of the present invention in order that the detailed description of the invention that follows may be better understood. Additional features and advantages of the invention will be described hereinafter that form the subject of the claims of the invention. It should be appreciated by those skilled in the art that the conception and the specific embodiments disclosed may be readily utilized as a basis for modifying or designing other embodiments for carrying out the same purposes of the present invention. It should also be realized by those skilled in the art that such equivalent embodiments do not depart from the spirit and scope of the invention as set forth in the appended claims.
- For a detailed description of the preferred embodiments of the invention, reference will now be made to the accompanying drawings in which:
-
FIG. 1 illustrates a sample analysis process including an accumulator and a sample collection apparatus; -
FIG. 2 illustrates an exploded view of an accumulator having a sample side comprising a flexible bag; -
FIG. 3 illustrates a sample analysis process including a sample collection apparatus and an accumulator comprising a flexible bag; -
FIG. 4 illustrates an accumulator; -
FIG. 5 illustrates a cross sectional side view of an embodiment of an accumulator in which the accumulator is purged by a purge gas; -
FIG. 6 illustrates a cross sectional side view of an embodiment of an accumulator in which a sample is being added to the accumulator; and -
FIG. 7 illustrates a cross sectional side view of an embodiment of an accumulator in which the accumulator is about full of sample gas. -
FIG. 1 illustrates asample analysis process 5 that includesaccumulator 10 and samplegas collection apparatus 15. Accumulator 10 is a sealed device suitable for allowing the transfer of sample gases at constant pressure. In embodiments as illustrated inFIGS. 1 and 2 ,accumulator 10 has a sealedchamber 30 that includes achamber separator 35 or aflexible bag 165. In alternative embodiments as illustrated inFIG. 3 ,accumulator 10 is aflexible bag 165. Accumulator 10 has a variable volume by which a variable volume ofsample gas 105 may be contained. It is to be understood that inFIG. 1 accumulator 10 is illustrated in a cross sectional side view. - In an embodiment as illustrated in
FIG. 1 ,accumulator 10 includeschamber 30,chamber separator 35,sample side 40, and.pressure side 45.Chamber separator 35 is a flexible membrane that separatessample side 40 frompressure side 45 and prevents the flow of any gas betweensample side 40 andpressure side 45. Chamber.separator 35 is secured tochamber 30 by any suitable means. -
FIG. 2 illustrates an exploded perspective view of an embodiment ofaccumulator 10 in whichaccumulator 10 includesflexible bag 165. In such embodiment,flexible bag 165 is attached to sampleorifice 20 to allowsample gas 105 to flow in and out offlexible bag 165. -
Chamber separator 35 andflexible bag 165 are flexible membranes that are impermeable by gas. In embodiments,chamber separator 35 andflexible bag 165 are flexible and impermeable by gas but are non-elastic. Without being limited by theory, elastic deformation ofchamber separator 35 orflexible bag 165 may impart varying pressure onsample gas 105, and in some embodiments a constant pressure is desired in the operation ofaccumulator 10. In an embodiment, the constant pressure is at atmospheric pressure. Further, without being limited by theory, a constant pressure is desired to eliminate the number of pumping, measuring, and regulating devices involved with pressurized systems.Chamber separator 35 andflexible bag 165 may be composed of any material that is flexible but non-elastic. Without limitation, examples of suitable materials forchamber separator 35 andflexible bag 165 include high density polyethylene or MYLAR, which is a registered trademark of E.I. Du Pont de Nemours and Company. In alternative embodiments,chamber separator 35 andflexible bag 165 may have a minimum amount of elasticity. In such alternative embodiments,chamber separator 35 andflexible bag 165 may be composed of any flexible and non gas permeable materials that exhibit elasticity. In some embodiments, the materials ofchamber separator 35 andflexible bag 165 are selected based on the, chemical nature of the gases involved and compatibility therewith. - As shown in
FIGS. 1-3 ,chamber 30 is composed of any materials suitable for supportingchamber separator 35. Without limitation,chamber 30 may be composed of acrylonitrile-butadiene-styrene (ABS), polycarbonate, polymethyl methacrylate (PMMA), aluminum, steel, plastic, or any combination thereof.FIG. 4 illustrates a perspective view ofaccumulator 10 showingchamber 30 having asample orifice 20 and apurge gas orifice 25.Sample orifice 20 may have any size and configuration suitable for allowingsample gas 105 to be introduced andexit accumulator 10.Purge gas orifice 25 may have any size and configuration suitable for allowing purge gas to be introduced andexit accumulator 10. It is to be understood thatFIG. 4 illustrates onesample orifice 20 and onepurge gas orifice 25. However,accumulator 10 is not limited to one oforifices FIG. 4 ,chamber 30 is composed of two portions that are secured to each other by securingmeans 50. Securing means 50 may include any securing means suitable for securing the two portions to each other, such as screws.Chamber 30 is not limited to the configuration and design ofFIG. 4 but instead may have any other suitable design and configuration for allowing the transfer ofsample gas 105 at constant pressure. - As further illustrated in
FIGS. 1 and 3 , samplegas collection apparatus 15 may include any method and apparatus for collecting a sample gas from a solid, liquid, or gas sample. Without limitation, examples of suitable methods for samplegas collection apparatus 15 include combustion, chemical reaction, catalytic reactions, and the like. Combustion may be accomplished by any suitable method such as by a combustion furnace.FIGS. 1 and 3 illustrate embodiments in which samplegas collection apparatus 15 is a combustion furnace for combusting asolid sample 85. The combustion furnace is not limited to the combustion furnace configuration illustrated inFIGS. 1 and 3 but instead may include any configuration for collecting a sample gas. - In an embodiment of the operation of
sample analysis process 5 as illustrated inFIG. 1 in which samplegas collection apparatus 15 is a vertical combustion furnace,combustion tube 80 is lifted into the furnace and combines withriser tube holder 95 to create a combustion chamber sealed against intrusion of atmospheric air or any other outside contaminants.Gas supply 60 provides agas 65 to samplegas collection apparatus 15. In an embodiment,gas supply 60 is a pressurized gas supply.Gas 65 is any combustion gas suitable for use in combustion ofsample 85. Without limitation, examples ofgas 65 include oxygen, air, and the like. In some embodiments,gas 65 is fed through avalve 70 and flowrestrictor 75 through riser tube, which may control the flow ofgas 65 to samplegas collection apparatus 15. Flow restrictor 75 is any flow restrictor such as a sintered metal frit that is suitable for restricting the flow of samplegas collection apparatus 15. In alternative embodiments,sample analysis process 5 does not includevalve 70 and/or flowrestrictor 75.Gas 65 is fed to sample gas collection apparatus .15 throughriser tube 90 to create an oxygen rich environment inside the furnace in which combustion takes place to combustsample 85, which is disposed onriser tube 90.Sample gas 105 flows out of samplegas collection apparatus 15 and intosample side 40 ofaccumulator 10. In some embodiments,sample gas 105 flows through catalyst in the end of the combustion chamber.Sample gas 105 includes the oxygen fromgas 65 and the products of combustion. In some embodiments,sample gas 105 may be passed throughwater removal apparatus 110 prior to being fed toaccumulator 10.Water removal apparatus 110 may be any device suitable for removing water or any other liquid fromsample gas 105. For instance,water removal apparatus 110 may be a particulate filter, a condensation trap, or the like. - In the embodiment illustrated in
FIG. 1 ,accumulator 10 includeschamber separator 35. In embodiments,accumulator 10 operates at atmospheric pressure.Accumulator 10 hasvalve 170 that connectspressure side 45 to vent 120.Vent 120 is a vent to the atmosphere. Whensample gas 105 is fed toaccumulator 10,valve 170 is open to vent 120, which allows any gas inpressure side 45 to escapeaccumulator 10 and thereby prevents the increasing volume ofsample gas 105 insample side 40 from resulting in an increased pressure inaccumulator 10. By allowing the sample volume to increase without an increase of pressure inaccumulator 10,sample gas 105 may be fed toaccumulator 10 at low pressures. Advantages of such atmospheric accumulation include allowing sample capture with a minimum number of pumps, regulators and flow control devices in the sample feed stream (i.e., sample gas 105). Without limitation, such additional components, if used, may lead to interferences (i.e., degradation) of the chemical compositions of sample gases and/or damage to the delicate and precision flow control devices, which may be caused by the nature of the sample gas streams. For instance,sample gas 105 may be corrosive and/or particulate bearing. In alternative embodiments (not illustrated),accumulator 10 may be operated at higher than atmospheric pressures. For instance, a backpressure regulator may be added betweenpressure side 45 and vent 120 to provide a constant, above atmospheric pressure. Advantages of higher than atmospheric pressures (i.e., compression) include allowing larger sample volume to be collected with a much smaller container (i.e., accumulator 10). -
FIGS. 5-7 illustrate adding volume ofsample gas 105 to an embodiment ofaccumulator 10 as illustrated inFIG. 1 in which accumulator 10 haschamber separator 35. In the embodiment ofFIG. 5 ,accumulator 10 is substantially full of gas onpressure side 45 with nosample gas 105 onsample side 40. In such an embodiment,accumulator 10 has about no volume onsample side 40.FIG. 6 illustrates an embodiment in which a volume ofsample gas 105 is being added toaccumulator 10 withchamber separator 35 preventingsample gas 105 from flowing topressure side 45.FIG. 7 illustrates an embodiment in which accumulator 10 is about full of a volume ofsample gas 105 with, nosample gas 105 flowing out ofaccumulator 10 throughpressure side 45. - As further illustrated in
FIG. 1 , when collection of the desired sample volume ofsample gas 105 is complete,valve 115 isolatessample side 40 from sample gas collection apparatus 15 (i.e., the combustion furnace).Valve 130 is switched to openaccumulator 10 toanalyzer 150, and a measured aliquot is pulled fromaccumulator 10 toanalyzer 150.Analyzer 150 may pull multiple aliquots of the same volume or different volumes ofsample gas 105 fromaccumulator 10. In some embodiments,sample gas 105 is stored inaccumulator 10 until it is desired for analysis.Analyzer 150 may include any analyzer suitable for analyzing a gas sample.Analyzer 150 analyzes a desired component ofsample gas 105. For instance, the analysis may include determining the amount of a component insample gas 105. The component may be any desired component such as carbon (i.e., total carbon analysis), nitrogen (i.e., total nitrogen analysis), sulfur, and the like. In an embodiment,analyzer 150 measures the amount of carbon insample gas 105. - As further illustrated in
FIG. 1 , when it is desired that no more ofsample gas 105 fromaccumulator 10 is to be analyzed,sample side 40 may be purged ofsample gas 105. Purging ofsample side 40 includes switchingvalve 130 to opensample side 40 to vent 120. In addition,valve 170 is switched to pressurizepressure side 45, which purgessample side 40 ofsample gas 105.FIG. 1 illustrates an embodiment in whichpressure side 45 is pressurized by thesame gas 65 that is fed to samplegas collection apparatus 15. In alternative embodiments (not illustrated),pressure side 45 is pressurized by a different gas thangas 65. Pressurization ofpressure side 45purges sample side 40 by increasing the pressure and volume onpressure side 45, which reduces the volume insample 40 andforces sample gas 105 out ofaccumulator 10 and to vent 120. After purgingsample side 40 ofsample gas 105,valve 170 is switched back to vent 120,valve 130 is switched away fromvent 120 and closed. In some embodiments,valve 135 is switched to allow gas 65 (or another purge gas) to flow intosample side 40 for a purge ofsample side 40.Valve 135 is then closed to the flow ofgas 65,valve 130 is opened to vent 120, andvalve 170 is opened to allow the flow ofgas 65 to fillpressure side 45 andpurge sample side 40 ofgas 65. In an embodiment, a timer controls the amount ofsample gas 105 andgas 65 fed to sampleside 40 andpressure side 45 duringsample analysis process 5. In an embodiment in which accumulator 10 includesflexible bag 165 disposed inchamber 30, the same operation steps as described for the above operation of the embodiment ofaccumulator 10 havingsample side 40 andchamber separator 35 apply, with it to be understood thatflexible bag 165 operationally takes the place of both thesample side 40 andchamber separator 35. - In an embodiment of the operation of
sample analysis process 5 as illustrated in.FIG. 3 in which accumulator 10 is aflexible bag 165,valve 130 is opened to vacuum 160, andvacuum 160 removes any gas inaccumulator 10. When it is desired forsample gas 105 to be fed toaccumulator 10 from samplegas collection apparatus 15,valve 130 is closed, andsample gas 105 is fed toaccumulator 10. When collection of the desired volume ofsample gas 105 is complete,valve 115 is switched to isolatesample gas 105 inaccumulator 10 from sample gas collection apparatus 15 (i.e., the combustion furnace).Valve 130 is switched to openaccumulator 10 toanalyzer 150, and a measured aliquot is pulled fromaccumulator 10 toanalyzer 150.Analyzer 150 may pull multiple aliquots of the same volume or different volumes ofsample gas 105 fromaccumulator 10. In some embodiments,sample gas 105 is stored inaccumulator 10 until it is desired for analysis. When it is desired that no more of thesample gas 105 inaccumulator 10 is to be analyzed,accumulator 10 may be purged ofsample gas 105. Purging ofaccumulator 10 includes switchingvalve 130 to openflexible bag 165 to vacuum 160, which purgesaccumulator 10 ofsample gas 105. In some embodiments,accumulator 10 may then be flushed by thesame gas 65 or by a different gas. In such embodiments, aftervacuum 160 purges accumulator 10 ofsample gas 105,valve 130 is closed, andvalve 135 allowsgas 65 to feed intoaccumulator 10. After the desired amount ofgas 65 is fed toaccumulator 10,valve 135 closes the flow ofgas 65, andvalve 130 is opened to vacuum 160, which purgesaccumulator 10 ofgas 65. In an embodiment, a timer controls the amount ofsample gas 105 andgas 65 fed toaccumulator 10 duringsample analysis process 5. - In alternative embodiments,
sample analysis process 5 may also includevalve 100, which allows a backflow ofgas 65 to preventcombustion tube 80 from being contaminated with atmospheric carbon dioxide. In some of such alternative embodiments,gas 65 may flow through aflow restrictor 125 beforevalve 100. - It is to be understood that the embodiments of
FIGS. 1 and 3 include usingflow restrictors sample analysis process 5 is not limited to use ofsuch flow restrictors flow restrictors - In alternative embodiments (not illustrated),
sample analysis process 5 does not include samplegas collection apparatus 15 but instead the desiredsample gas 105 to be analyzed is provided and fed toaccumulator 10 withsample analysis process 5 operating otherwise as described above. - In other alternative embodiments,
chamber separator 35 andflexible bag 165 are elastic. In such alternative embodiments,sample side 40 andflexible bag 165 are not fully filled withsample 105, which prevents elastic deformation ofchamber separator 35 andflexible bag 165 fromsample gas 105 and allows a constant pressure inaccumulator 10. - Therefore,
sample analysis process 5 includingaccumulator 10 provides the advantage of regulating the amount ofsample gas 105 passed toanalyzer 150. Additional advantages include the ability to storesample gas 105 for analysis at a later time. Further advantages provided include adjusting the size of samples (i.e., the aliquots) fed to analyzer 150 as well as allowing repeated samples of the same size to be fed toanalyzer 150. For instance, in some embodiments, small aliquots ofsample gas 105 may be desired for analysis for high carbon content, and large aliquots ofsample gas 105 may be desired for low carbon content. Consequently,sample analysis process 5 provides a reservoir (i.e., accumulator 10) to provide a broad range of sample sizes for a multitude of measurements. - Although the present invention and its advantages have been described in detail, it should be understood that various changes, substitutions and alterations may be made herein without departing from the spirit and scope of the invention as defined by the appended claims.
Claims (25)
1. A sample-gas dispensing system, comprising:
a sample gas source, configured to feed a sample gas;
a variable-volume accumulator configured to accumulate an increasing volume of the sample gas;
an analyzer, wherein the variable-volume accumulator is configured to dispense a first aliquot of the sample gas to the analyzer,
wherein the variable-volume accumulator is simultaneously coupled to the sample gas source and the analyzer.
2. The system of claim 1 , wherein the accumulator comprises a chamber, and wherein the chamber comprises a sample side and a pressure side, and further wherein the sample side contains a variable volume of the sample gas.
3. The system of claim 2 , wherein the chamber comprises a chamber separator that separates the sample side from the pressure side and prevents flow of gas between the sample side and the pressure side, and wherein the chamber separator comprises a flexible membrane that is impermeable by gas.
4. The system of claim 2 , wherein the chamber comprises a flexible bag that prevents flow of sample gas to the pressure side, and wherein the flexible bag is impermeable by gas.
5. The system of claim 2 , wherein a valve allows the pressure side to be open to the atmosphere when the sample gas is fed to the sample side.
6. The system of claim 2 , wherein a purge gas fed to the pressure side forces the sample gas out of the sample side, and wherein a valve closes the sample side to the analyzer and opens the sample side to a vent to atmosphere.
7. The system of claim 1 , wherein the accumulator comprises a flexible bag that is impermeable by gas.
8. The system of claim 7 , further comprising a vacuum, wherein the vacuum removes sample gas from the flexible bag.
9. The system of claim 8 , wherein a purge gas is fed to the flexible bag to purge the flexible bag after the vacuum removes the sample gas from the flexible bag.
10. The system of claim 9 , wherein the purge gas is removed from the flexible bag by the vacuum.
11. The system of claim 1 , wherein the sample gas source comprises a combustion furnace.
12. The system of claim 1 , wherein the system is operated at atmospheric pressure.
13. The system of claim 1 , wherein the accumulator comprises a single gas orifice, wherein the single gas orifice is simultaneously coupled with the sample gas source and the analyzer.
14. The system of claim 1 , wherein the accumulator comprises a single gas orifice, wherein the single gas orifice is simultaneously coupled with the variable-volume sample gas source and a purge gas source or a vacuum.
15. The system of claim 1 , wherein the variable-volume accumulator is configured to dispense a second aliquot of sample gas to the analyzer.
16. The system of claim 15 , wherein the second aliquot of sample gas has a different volume than the first aliquot of sample gas.
17. A sample-gas dispensing system, comprising:
a sample gas source;
a sample gas analyzer;
accumulator means for accumulating sample gas in a variable volume and releasing first and second aliquots of sample gas to the sample gas analyzer,
wherein the sample gas source, the accumulator means, and the sample gas analyzer are simultaneously coupled together.
18. The apparatus of claim 17 , wherein the accumulator means comprises a chamber, and wherein the chamber comprises a variable-volume sample side and a pressure side.
19. The apparatus of claim 18 , wherein the chamber comprises a gas-impermeable flexible membrane interposed between the sample side and the pressure side.
20. The apparatus of claim 17 , wherein the accumulator means comprises a flexible bag that is impermeable by gas.
21. The, apparatus of claim 20 , further comprising means for purging the flexible bag of the sample gas by a vacuum.
22. The apparatus of claim 17 , wherein the volume of sample gas in the second aliquot is different from the volume of sample gas in the first aliquot.
23. The system of claim 17 wherein the sample gas source comprises a combustion furnace.
24. A sample-gas dispensing system, comprising:
a combustion furnace configured to emit a sample gas;
a variable-volume flexible bag coupled to the combustion furnace, the variable-volume flexible bag configured to accumulate an increasing volume of the sample gas emitted by the combustion furnace;
an analyzer coupled to the variable-volume flexible bag; and
means for dispensing a first aliquot and a second aliquot of sample gas from the variable-volume flexible bag to the analyzer.
25. The system of claim 24 . wherein the first and second aliquots have different volumes.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US13/482,983 US20120247188A1 (en) | 2007-05-15 | 2012-05-29 | Gas Sample Collection and Analysis |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US91795507P | 2007-05-15 | 2007-05-15 | |
US12/121,589 US8191437B2 (en) | 2007-05-15 | 2008-05-15 | Gas sample collection and analysis |
US13/482,983 US20120247188A1 (en) | 2007-05-15 | 2012-05-29 | Gas Sample Collection and Analysis |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US12/121,589 Continuation US8191437B2 (en) | 2007-05-15 | 2008-05-15 | Gas sample collection and analysis |
Publications (1)
Publication Number | Publication Date |
---|---|
US20120247188A1 true US20120247188A1 (en) | 2012-10-04 |
Family
ID=41419730
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US12/121,589 Active 2029-03-10 US8191437B2 (en) | 2007-05-15 | 2008-05-15 | Gas sample collection and analysis |
US13/482,983 Abandoned US20120247188A1 (en) | 2007-05-15 | 2012-05-29 | Gas Sample Collection and Analysis |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US12/121,589 Active 2029-03-10 US8191437B2 (en) | 2007-05-15 | 2008-05-15 | Gas sample collection and analysis |
Country Status (2)
Country | Link |
---|---|
US (2) | US8191437B2 (en) |
WO (1) | WO2009151864A1 (en) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8191437B2 (en) | 2007-05-15 | 2012-06-05 | O.I. Corporation | Gas sample collection and analysis |
CA2790035A1 (en) * | 2010-02-26 | 2011-09-01 | Gueorgui M. Mihaylov | Container for fluid sampling with flexible metal alloy walls |
KR102365503B1 (en) * | 2019-12-24 | 2022-02-21 | 주식회사 태성환경연구소 | A method and apparatus for capturing odor |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5142143A (en) * | 1990-10-31 | 1992-08-25 | Extrel Corporation | Method and apparatus for preconcentration for analysis purposes of trace constitutes in gases |
US5981912A (en) * | 1996-02-01 | 1999-11-09 | Bodenseewerk Perkin-Elmer Gmbh | Electrothermal atomization means for analytical spectrometry |
US20050262928A1 (en) * | 2001-01-31 | 2005-12-01 | Lennart Bjork | Sampling apparatus |
US20060117841A1 (en) * | 2004-12-07 | 2006-06-08 | Petroleum Habitats, L.L.C. | Novel well logging method for the determination of catalytic activity |
US7225690B1 (en) * | 2002-08-02 | 2007-06-05 | A+ Manufacturing, Llc | Multi-cavity sample cylinder with integrated valving |
US8191437B2 (en) * | 2007-05-15 | 2012-06-05 | O.I. Corporation | Gas sample collection and analysis |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4008393A (en) * | 1970-09-11 | 1977-02-15 | Intertechnique S.A. | System and method of liquid scintillation counting |
GB1423232A (en) * | 1972-03-07 | 1976-02-04 | Matsushita Electric Ind Co Ltd | Apparatus for burning sample materials and collecting the combustion gases |
US4336127A (en) * | 1981-05-26 | 1982-06-22 | Chevron Research Company | Staged burning of retorted carbon-containing solids |
AT393565B (en) * | 1988-08-09 | 1991-11-11 | Avl Verbrennungskraft Messtech | DISPOSABLE MEASURING ELEMENT |
US5303599A (en) * | 1992-07-29 | 1994-04-19 | Welker Engineering Company | Miniaturized sampler |
DE19616760C2 (en) * | 1996-04-26 | 1999-12-23 | Fraunhofer Ges Forschung | Method and device for the continuous determination of gaseous oxidation products |
US6016841A (en) * | 1997-08-27 | 2000-01-25 | Autoliv Asp, Inc. | Accumulator with low permeability flexible diaphragm |
US20020064881A1 (en) * | 2000-11-30 | 2002-05-30 | Devlin William Jackson | Method for automatically storing and reprocessing patient specimen's in an automatic clinical analyzer |
IL148468A (en) * | 2002-03-03 | 2012-12-31 | Exalenz Bioscience Ltd | Breath collection system |
-
2008
- 2008-05-15 US US12/121,589 patent/US8191437B2/en active Active
-
2009
- 2009-05-14 WO PCT/US2009/044040 patent/WO2009151864A1/en active Application Filing
-
2012
- 2012-05-29 US US13/482,983 patent/US20120247188A1/en not_active Abandoned
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5142143A (en) * | 1990-10-31 | 1992-08-25 | Extrel Corporation | Method and apparatus for preconcentration for analysis purposes of trace constitutes in gases |
US5981912A (en) * | 1996-02-01 | 1999-11-09 | Bodenseewerk Perkin-Elmer Gmbh | Electrothermal atomization means for analytical spectrometry |
US20050262928A1 (en) * | 2001-01-31 | 2005-12-01 | Lennart Bjork | Sampling apparatus |
US7213474B2 (en) * | 2001-01-31 | 2007-05-08 | Astrazeneca Ab | Sampling apparatus |
US7225690B1 (en) * | 2002-08-02 | 2007-06-05 | A+ Manufacturing, Llc | Multi-cavity sample cylinder with integrated valving |
US20060117841A1 (en) * | 2004-12-07 | 2006-06-08 | Petroleum Habitats, L.L.C. | Novel well logging method for the determination of catalytic activity |
US8191437B2 (en) * | 2007-05-15 | 2012-06-05 | O.I. Corporation | Gas sample collection and analysis |
Also Published As
Publication number | Publication date |
---|---|
WO2009151864A1 (en) | 2009-12-17 |
US8191437B2 (en) | 2012-06-05 |
US20080307903A1 (en) | 2008-12-18 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US10161920B2 (en) | Analytical system and method for detecting volatile organic compounds in water | |
CN107430044B (en) | System and method for testing gas leakage through gas flow components | |
JP4018737B2 (en) | System and method for extracting headspace vapor | |
EP2876438B1 (en) | Head space sample introduction device and gas chromatograph including same | |
KR101442064B1 (en) | In insulating oil gas analyzer apparatus and method | |
WO2008060165A1 (en) | Improvements in or relating to breath collection methods and apparatus | |
US10408746B2 (en) | System and method for impurity detection in beverage grade gases | |
TWI642936B (en) | Apparatus and method for analyzing breath gas mixture for halitosis detection | |
US20120247188A1 (en) | Gas Sample Collection and Analysis | |
CZ291746B6 (en) | Method of environmental monitoring of low concentration levels of organic compounds in an environmental medium and apparatus for making the same | |
JP4361936B2 (en) | Method for introducing standard gas into a sample vessel | |
EP1148337B1 (en) | Method for analyzing impurities in a gas stream | |
US20050120775A1 (en) | Systems and methods for detecting contaminants | |
JP4472893B2 (en) | Odor measurement method | |
EP2167953B1 (en) | Gas sample collection and analysis | |
JP4527110B2 (en) | Analyzer having variable volume type ballast chamber and analysis method | |
US20190086376A1 (en) | Analysis device and method | |
US8557023B2 (en) | Device for preparing a gas flow for introduction thereof into a mass spectrometer | |
US9182325B2 (en) | Method and apparatus for changing relative concentrations of gases present within a gaseous sample for mass spectrometry | |
JP7029252B2 (en) | Hydrogen gas analysis kit, hydrogen gas analysis method and hydrogen gas quality control method | |
RU2408863C1 (en) | Sample container for taking samples of human expired air on molecular markers | |
Sanchez et al. | Performance characteristics of a new prototype for a portable GC using ambient air as carrier gas for on‐site analysis | |
US8875559B2 (en) | System and method for measuring the concentration of impurities mixed with hydrogen gas | |
US20230364610A1 (en) | Membrane inlet for chemical analysis with sample degassing | |
US6368559B1 (en) | Device for analyzing organic compounds particularly in aqueous and gaseous samples |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
STCB | Information on status: application discontinuation |
Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION |