US20100047127A1 - Conditioning slurry samples for quantitative instrumental analysis - Google Patents
Conditioning slurry samples for quantitative instrumental analysis Download PDFInfo
- Publication number
- US20100047127A1 US20100047127A1 US12/588,897 US58889709A US2010047127A1 US 20100047127 A1 US20100047127 A1 US 20100047127A1 US 58889709 A US58889709 A US 58889709A US 2010047127 A1 US2010047127 A1 US 2010047127A1
- Authority
- US
- United States
- Prior art keywords
- slurry
- liquid phase
- filtration
- vacuum
- filtration unit
- 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
- 239000002002 slurry Substances 0.000 title claims abstract description 40
- 238000004458 analytical method Methods 0.000 title abstract description 8
- 230000003750 conditioning effect Effects 0.000 title abstract description 8
- 239000007791 liquid phase Substances 0.000 claims abstract description 15
- 239000000706 filtrate Substances 0.000 claims abstract description 10
- 239000007790 solid phase Substances 0.000 claims abstract description 5
- 239000007788 liquid Substances 0.000 claims abstract description 4
- 238000001914 filtration Methods 0.000 claims description 31
- 239000000523 sample Substances 0.000 claims description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 14
- 238000004891 communication Methods 0.000 claims description 8
- 238000005259 measurement Methods 0.000 claims description 7
- 230000000694 effects Effects 0.000 claims description 2
- 230000004044 response Effects 0.000 claims description 2
- 238000000926 separation method Methods 0.000 claims description 2
- 238000000034 method Methods 0.000 abstract description 10
- 230000008569 process Effects 0.000 abstract description 5
- XTEGARKTQYYJKE-UHFFFAOYSA-M Chlorate Chemical compound [O-]Cl(=O)=O XTEGARKTQYYJKE-UHFFFAOYSA-M 0.000 abstract description 4
- OSVXSBDYLRYLIG-UHFFFAOYSA-N dioxidochlorine(.) Chemical compound O=Cl=O OSVXSBDYLRYLIG-UHFFFAOYSA-N 0.000 description 12
- 239000004155 Chlorine dioxide Substances 0.000 description 6
- 238000001069 Raman spectroscopy Methods 0.000 description 6
- 235000019398 chlorine dioxide Nutrition 0.000 description 6
- BZSXEZOLBIJVQK-UHFFFAOYSA-N 2-methylsulfonylbenzoic acid Chemical compound CS(=O)(=O)C1=CC=CC=C1C(O)=O BZSXEZOLBIJVQK-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 238000007705 chemical test Methods 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 239000012429 reaction media Substances 0.000 description 3
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 238000007605 air drying Methods 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 238000002425 crystallisation Methods 0.000 description 2
- 230000008025 crystallization Effects 0.000 description 2
- 238000004255 ion exchange chromatography Methods 0.000 description 2
- 239000012071 phase Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 239000011260 aqueous acid Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 238000001311 chemical methods and process Methods 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 230000001143 conditioned effect Effects 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 150000004691 decahydrates Chemical class 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000010587 phase diagram Methods 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000004886 process control Methods 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 238000005070 sampling Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000011555 saturated liquid Substances 0.000 description 1
- RSIJVJUOQBWMIM-UHFFFAOYSA-L sodium sulfate decahydrate Chemical compound O.O.O.O.O.O.O.O.O.O.[Na+].[Na+].[O-]S([O-])(=O)=O RSIJVJUOQBWMIM-UHFFFAOYSA-L 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000003828 vacuum filtration Methods 0.000 description 1
- 238000009834 vaporization Methods 0.000 description 1
- 230000008016 vaporization Effects 0.000 description 1
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
- G01N1/28—Preparing specimens for investigation including physical details of (bio-)chemical methods covered elsewhere, e.g. G01N33/50, C12Q
- G01N1/40—Concentrating samples
- G01N1/4077—Concentrating samples by other techniques involving separation of suspended solids
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T436/00—Chemistry: analytical and immunological testing
- Y10T436/25—Chemistry: analytical and immunological testing including sample preparation
- Y10T436/25375—Liberation or purification of sample or separation of material from a sample [e.g., filtering, centrifuging, etc.]
Definitions
- the present invention is concerned with rendering slurry samples suitable for instrumental analysis.
- the present invention provides a method and system for consistently and automatically conditioning and delivering a solids-free liquid (filtrate) sample suitable for instrumental analyses. While the present invention is described in detail with respect to slurries from chlorine dioxide generating plants, it will be clear to a person skilled in the art that the principles described herein are applicable to all types of slurries encountered in industrial processes.
- a method of measuring the concentration of at least one dissolved component in the liquid phase of a slurry which comprises providing an analytical unit comprising an inlet chamber for said slurry in communication with an inlet, a filtration medium for removing the solid phase from the slurry located downstream of the inlet chamber, and a chamber downstream of the filter in communication with an outlet, feeding said slurry to said inlet, then through said filtration medium to separate said solid phase from the liquid phase with the liquid phase passing into the chamber until a predetermined amount of said liquid phase has entered said chamber, and measuring the concentration of the at least one dissolved component in the liquid phase in said chamber.
- an analytical system for measuring the concentration of at least one dissolved component in the liquid phase of a slurry, which comprises a slurry filtration unit comprising a filtration cell comprising an inlet for the slurry to a slurry chamber, a filtration medium for separation of the solid phase from the slurry, and a liquid phase chamber downstream of said filtration medium and having an outlet therefrom, said liquid phase chamber having a liquid level sensor and a concentration measurement probe in operable association therewith, a utility system in operable relationship with said slurry filtrate unit for selectively applying compressed air, water and vacuum to the outlet from said slurry filtration unit, and a control/communication system in operable relationship with said slurry filtration unit and said utility system for controlling the operation of the analytical system in response to a pre-programmed set of commands
- FIG. 1 is a graphical representation of experiments conducted comparing the concentration of sodium chlorate in a chlorine dioxide-generating reaction medium, measured by Raman spectrometer in comparison to chemical tests;
- FIG. 2 contains a schematic illustration of a slurry conditioning system provided in accordance with a preferred embodiment of the invention and comprising a slurry filtration unit (SFU), a utility system (US) and a control/communication system (CCS).
- SFU slurry filtration unit
- US utility system
- CCS control/communication system
- a slurry conditioning system 10 includes a slurry filtration unit (SFU) 11 , a utility system (US) 12 and a control/communication system (CCS) 13 .
- the SFU is a filtration cell (FC) 16 , equipped with a level sensor 17 , a temperature sensor 18 and an instrument probe 19 .
- the FC filtration cell 16 consists of an upper chamber (UC) 22 separated from a lower chamber (LC) 24 by a filtration medium (FM) 26 .
- the filtration medium 26 may be of variable size and material of construction, depending on the nature of the slurry to be processed.
- An upper port (P 1 ) 28 is connected to the utility assembly 12 .
- Other ports are provided for the level sensor 17 , temperature sensor 18 and instrument probe 19 .
- a lower port (P 2 ) 29 connects the lower chamber 24 to the process from which the slurry to be tested is taken.
- This unit 11 may be used to introduce a probe of any kind for instrumental analyses of the filtered sample, such as IC (ion chromatography), Raman spectroscopy, FT-NIR (Fourier Transform-Near Infra Red) or the like.
- IC ion chromatography
- Raman spectroscopy Raman spectroscopy
- FT-NIR Fast Fourier Transform-Near Infra Red
- the utility system 12 comprises several solenoid valves, namely hot water SV 1 38 , compressed air SV 2 40 , vacuum SV 3 42 and vacuum relief SV 4 44 .
- the arrangement of all connections is to at least minimize and preferably eliminate chances to leave residual water in the cell 16 which could later dilute the filtered sample and result in errors. This consideration is particularly important when the sample volume is to be reduced as much as possible.
- vacuum can be used to create a pressure differential and render filtrate free of solids.
- the incoming slurry stream via P 2 29 may be forced through the filtration media FM 26 in its entirety (called dead end filtration).
- the method of this invention generally proceeds in cycles involving a number of steps, namely 1) air blow, 2) water washing, 3) air drying, 4) filtration under vacuum, 5) vacuum relief and 6) measurement.
- the steps 1 to 3 may be repeated more than once should difficulty in filter medium cleaning be encountered.
- the duration of each step as well as the temperature and pressure conditions in each step are determined based on the characteristics of each slurry treated. A representative Example appears below.
- the program in a Programmable Logic Controller (PLC) 46 closes the vacuum valve SV 3 42 , marking the end of filtration. While the filtrate comes to the upper chamber 22 that is at sub-atmospheric pressure, dissolved gas (chlorine dioxide) is disengaged from the liquid phase, forming bubbles, exerting serious interruptions to the analysis. It has been found that the vacuum can be released to a certain degree by opening SV 4 44 for a given time until gas bubbles disappear and the gas phase interference is eliminated.
- PLC Programmable Logic Controller
- water and air temperature are also critical parameters. If no limitation exists, any available temperature in the 10° to 70° C. [see 80° C. below] range may be used. However, for chlorine dioxide generator liquor, it was observed that crystallization can take place in the saturated liquid should the filtrate temperature fall below 40° C. Strictly speaking, the phase diagram has a change at temperature 32° C. below which sodium sulphate decahydrate would precipitate. Due to the reversed relationship of solubility versus temperature when the temperature is above 32° C., the filtrate at its usually initial temperature of 70° C. can remain clear until it cools down to near or below this critical temperature related to the phase change.
- the preferred embodiment employs hot water with a temperature in the range of about 50° to about 80° C.
- a temperature in the range of about 50° to about 80° C.
- the PLC 46 controls the sequence of operations based on the program and signals received.
- the output from PLC 46 are signals to activate/deactivate individual solenoid valves.
- the specific instrument probe starts measurement as the instrument 47 receives a trigger from PLC 46 .
- the signal of the probe is sent to a site computer PC 48 where it is converted to a standard signal that is transmitted to the DCS (Distributed Control System).
- This Example illustrates a conditioning cycle for the filtration system described in reference to FIG. 2 and equipped with a Raman laser probe that transmits spectra to Raman spectrometer as the analytical instrument.
- Hot water temperature 70° C.
- Hot water pressure 15 psig
- Compressed air pressure 20 psig
- Compressed air temperature Room temperature Vacuum (maximum): 25 in.Hg
- Vacuum relief low limit 10 to 15 in.Hg
- the present invention provides a novel system and procedure for consistently and automatically conditioning slurries and obtaining good filtrate sample for instrumental analyses. Modifications are possible within the scope of the invention.
Landscapes
- Physics & Mathematics (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (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)
- Investigating, Analyzing Materials By Fluorescence Or Luminescence (AREA)
- Investigating Or Analyzing Non-Biological Materials By The Use Of Chemical Means (AREA)
Abstract
A method and system to consistently and automatically conditioning and delivering a solid-free liquid (filtrate) sample suitable for instrumental analysis is disclosed. A slurry, preferably a slurry produced by a sub-atmospheric pressure chlorate dioxide generating process, is fed through a filter to remove the solid phase and to provide the liquid phase on the downstream side of the filter, where the concentration of at least one dissolved component is determined.
Description
- The present invention is concerned with rendering slurry samples suitable for instrumental analysis.
- The vast majority of chemical processes to generate chlorine dioxide currently in commercial use in pulp mills take place under sub-atmospheric conditions. In such processes, chlorine dioxide is generated by reducing sodium chlorate using a reducing agent, such as methanol or hydrogen peroxide, in an aqueous acid reaction medium containing sulfuric acid maintained at its boiling point under a sub-atmospheric pressure. The reaction medium in such processes is a slurry with a solids content commonly ranging from about 10 to about 30% w/w. The two major parameters in terms of the concentration control in the reactor, namely chlorate molarity and titratable acidity, are normally maintained within target bands no wider than +/−about 0.2 M and +/−about 0.2 N, respectively. Such control targets are accomplished based on analytical results of chemical tests performed manually by plant operators.
- Being able to continuously monitor liquor composition is desirable beyond the obvious manpower savings. The accuracy and precision of process control that would be achieved by means of on-line measurement would ultimately lead to higher reaction efficiency and lower chemical consumptions. But all known attempts to meet the above analytical requirements without human intervention have not been successful or not in sustainable and reliable services. One of the reasons is the difficulty inherent to the sampling of hot and saturated slurry-type process streams.
- The present invention provides a method and system for consistently and automatically conditioning and delivering a solids-free liquid (filtrate) sample suitable for instrumental analyses. While the present invention is described in detail with respect to slurries from chlorine dioxide generating plants, it will be clear to a person skilled in the art that the principles described herein are applicable to all types of slurries encountered in industrial processes.
- In accordance with one aspect of the present invention, there is provided a method of measuring the concentration of at least one dissolved component in the liquid phase of a slurry, which comprises providing an analytical unit comprising an inlet chamber for said slurry in communication with an inlet, a filtration medium for removing the solid phase from the slurry located downstream of the inlet chamber, and a chamber downstream of the filter in communication with an outlet, feeding said slurry to said inlet, then through said filtration medium to separate said solid phase from the liquid phase with the liquid phase passing into the chamber until a predetermined amount of said liquid phase has entered said chamber, and measuring the concentration of the at least one dissolved component in the liquid phase in said chamber.
- In accordance with another aspect of the present invention, there is provided an analytical system for measuring the concentration of at least one dissolved component in the liquid phase of a slurry, which comprises a slurry filtration unit comprising a filtration cell comprising an inlet for the slurry to a slurry chamber, a filtration medium for separation of the solid phase from the slurry, and a liquid phase chamber downstream of said filtration medium and having an outlet therefrom, said liquid phase chamber having a liquid level sensor and a concentration measurement probe in operable association therewith, a utility system in operable relationship with said slurry filtrate unit for selectively applying compressed air, water and vacuum to the outlet from said slurry filtration unit, and a control/communication system in operable relationship with said slurry filtration unit and said utility system for controlling the operation of the analytical system in response to a pre-programmed set of commands
-
FIG. 1 is a graphical representation of experiments conducted comparing the concentration of sodium chlorate in a chlorine dioxide-generating reaction medium, measured by Raman spectrometer in comparison to chemical tests; and -
FIG. 2 contains a schematic illustration of a slurry conditioning system provided in accordance with a preferred embodiment of the invention and comprising a slurry filtration unit (SFU), a utility system (US) and a control/communication system (CCS). - Referring to
FIG. 2 , aslurry conditioning system 10 includes a slurry filtration unit (SFU) 11, a utility system (US) 12 and a control/communication system (CCS) 13. The SFU is a filtration cell (FC) 16, equipped with a level sensor 17, atemperature sensor 18 and aninstrument probe 19. - The FC filtration cell 16 consists of an upper chamber (UC) 22 separated from a lower chamber (LC) 24 by a filtration medium (FM) 26. The filtration medium 26 may be of variable size and material of construction, depending on the nature of the slurry to be processed. An upper port (P1) 28 is connected to the
utility assembly 12. Other ports are provided for the level sensor 17,temperature sensor 18 andinstrument probe 19. A lower port (P2) 29 connects thelower chamber 24 to the process from which the slurry to be tested is taken. - This
unit 11 may be used to introduce a probe of any kind for instrumental analyses of the filtered sample, such as IC (ion chromatography), Raman spectroscopy, FT-NIR (Fourier Transform-Near Infra Red) or the like. - The
utility system 12 comprises several solenoid valves, namely hot water SV1 38, compressed air SV2 40,vacuum SV3 42 and vacuum relief SV4 44. The arrangement of all connections is to at least minimize and preferably eliminate chances to leave residual water in the cell 16 which could later dilute the filtered sample and result in errors. This consideration is particularly important when the sample volume is to be reduced as much as possible. - In operation, vacuum can be used to create a pressure differential and render filtrate free of solids. The incoming slurry stream via P2 29 may be forced through the filtration media FM 26 in its entirety (called dead end filtration). The method of this invention generally proceeds in cycles involving a number of steps, namely 1) air blow, 2) water washing, 3) air drying, 4) filtration under vacuum, 5) vacuum relief and 6) measurement. The
steps 1 to 3 may be repeated more than once should difficulty in filter medium cleaning be encountered. The duration of each step as well as the temperature and pressure conditions in each step are determined based on the characteristics of each slurry treated. A representative Example appears below. - In the approach of applying a vacuum as driving force for filtration, as the filtrate level rises high enough to reach the level sensor L 17, the program in a Programmable Logic Controller (PLC) 46, closes the
vacuum valve SV3 42, marking the end of filtration. While the filtrate comes to theupper chamber 22 that is at sub-atmospheric pressure, dissolved gas (chlorine dioxide) is disengaged from the liquid phase, forming bubbles, exerting serious interruptions to the analysis. It has been found that the vacuum can be released to a certain degree by opening SV4 44 for a given time until gas bubbles disappear and the gas phase interference is eliminated. - Depending on the particular slurry being conditioned, water and air temperature are also critical parameters. If no limitation exists, any available temperature in the 10° to 70° C. [see 80° C. below] range may be used. However, for chlorine dioxide generator liquor, it was observed that crystallization can take place in the saturated liquid should the filtrate temperature fall below 40° C. Strictly speaking, the phase diagram has a change at temperature 32° C. below which sodium sulphate decahydrate would precipitate. Due to the reversed relationship of solubility versus temperature when the temperature is above 32° C., the filtrate at its usually initial temperature of 70° C. can remain clear until it cools down to near or below this critical temperature related to the phase change.
- From the standpoint of promoting the filtration rate by reducing the slurry viscosity, or preventing the formation of decahydrate fine particulates in the filtered sample, it is essential to maintain the filtration cell temperature well above 40° C.
- It is particularly challenging to accomplish such thermostatic conditions when performing vacuum filtration due to the cooling effect of water vaporization in UC 22.
- For the reasons expressed above, the preferred embodiment employs hot water with a temperature in the range of about 50° to about 80° C. In cases where it is difficult to maintain the cell 16 at the temperature needed to prevent crystallization, it may be necessary to surround the SFU 11 with an enclosure and supply hot air or heating.
- The PLC 46 controls the sequence of operations based on the program and signals received. The output from
PLC 46 are signals to activate/deactivate individual solenoid valves. The specific instrument probe starts measurement as the instrument 47 receives a trigger fromPLC 46. The signal of the probe is sent to a site computer PC 48 where it is converted to a standard signal that is transmitted to the DCS (Distributed Control System). - This Example illustrates a conditioning cycle for the filtration system described in reference to
FIG. 2 and equipped with a Raman laser probe that transmits spectra to Raman spectrometer as the analytical instrument. - The conditioning cycle proceeds in accordance with Table I below:
-
TABLE I Output Typical SV4 duration Input SV1 SV2 SV3 (Vacuum Step Action (sec) Level (water) (air) (vacuum) relief) Trigger 1 Air blow 20 open close open close close inactive 2 Water washing 120 open open close close close inactive 3 Air drying 120 open close open close close inactive 4 Vacuuming/ L controlled close close close open close inactive Filtering 5 Vacuum relief 30 close close close close open inactive 6 Stabilization 30 close close close close close inactive 7 Raman 300 close close close close close active measurement Next cycle starts - Hot water temperature: 70° C.
Hot water pressure: 15 psig
Compressed air pressure: 20 psig
Compressed air temperature: Room temperature
Vacuum (maximum): 25 in.Hg
Vacuum relief low limit: 10 to 15 in.Hg - A comparison was made of instrumental analysis carried out as described above to provide Raman spectrometer measurements with chemical tests on the sodium chlorate concentration in a slurry from a chlorine dioxide generator. The results are presented graphically in
FIG. 1 , from which it can be seen that there is close correlation of the data. - In summary of this disclosure, the present invention provides a novel system and procedure for consistently and automatically conditioning slurries and obtaining good filtrate sample for instrumental analyses. Modifications are possible within the scope of the invention.
Claims (6)
1.-10. (canceled)
11. An analytical system for measuring the concentration of at least one dissolved component in the liquid phase of a slurry, which comprises:
a slurry filtration unit comprising a filtration cell comprising an inlet for the slurry to a slurry chamber, a filtration medium for separation of the solid phase from the slurry, and a liquid phase chamber downstream of said filtration medium and having an outlet therefrom, said liquid phase chamber having a liquid level sensor and a concentration measurement probe in operable association therewith,
a utility system in operable relationship with said slurry filtrate unit for selectively applying compressed air, water and vacuum to the outlet from said slurry filtration unit, and
a control/communication system in operable relationship with said slurry filtration unit and said utility system for controlling the operation of the analytical system in response to a pre-programmed set of commands.
12. The system of claim 11 , wherein said liquid phase chamber additionally has a temperature sensor in operable association therewith.
13. The system of claim 11 wherein said utility system comprises a plurality of solenoid valves separately connected to respective sources of compressed air, water and vacuum to permit the compressed air, water and vacuum to be selectively applied to the outlet from the filtration unit in accordance with a predetermined set of commands to said solenoid valves provided by said control/communication system.
14. The system of claim 12 further including a further solenoid valve operatively connected to the outlet from said slurry filtration unit to permit vacuum relief to said liquid phase chamber.
15. The system of claim 14 wherein said control/communication system possesses a pre-programmed set of commands to effect the operation of the analytic system in accordance with the cycle of operation set forth in Table I.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US12/588,897 US20100047127A1 (en) | 2005-04-14 | 2009-11-02 | Conditioning slurry samples for quantitative instrumental analysis |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US67108505P | 2005-04-14 | 2005-04-14 | |
| US11/402,946 US7651865B2 (en) | 2005-04-14 | 2006-04-13 | Conditioning slurry samples for quantitative instrumental analysis |
| US12/588,897 US20100047127A1 (en) | 2005-04-14 | 2009-11-02 | Conditioning slurry samples for quantitative instrumental analysis |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US11/402,946 Division US7651865B2 (en) | 2005-04-14 | 2006-04-13 | Conditioning slurry samples for quantitative instrumental analysis |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US13/898,417 Continuation US20130260269A1 (en) | 2004-02-10 | 2013-05-20 | Method and apparatus for operating a solid-oxide fuel cell stack with a mixed ionic/electronic conducting electrolyte |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US20100047127A1 true US20100047127A1 (en) | 2010-02-25 |
Family
ID=37101501
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US11/402,946 Active 2027-09-27 US7651865B2 (en) | 2005-04-14 | 2006-04-13 | Conditioning slurry samples for quantitative instrumental analysis |
| US12/588,897 Abandoned US20100047127A1 (en) | 2005-04-14 | 2009-11-02 | Conditioning slurry samples for quantitative instrumental analysis |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US11/402,946 Active 2027-09-27 US7651865B2 (en) | 2005-04-14 | 2006-04-13 | Conditioning slurry samples for quantitative instrumental analysis |
Country Status (2)
| Country | Link |
|---|---|
| US (2) | US7651865B2 (en) |
| CA (1) | CA2543385C (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103630427A (en) * | 2013-11-25 | 2014-03-12 | 北京矿冶研究总院 | Automatic ore pulp filtering and sampling device |
Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3637079A (en) * | 1967-07-12 | 1972-01-25 | Filtrox Maschinenbau Ag | Filter and method of cleaning the filter |
| US5104553A (en) * | 1987-12-23 | 1992-04-14 | Oerlikon-Contraves Ag | Apparatus for filtering a reagent |
| US6134952A (en) * | 1997-09-18 | 2000-10-24 | Alberta Research Council Inc. | Dissolved solid analyzer |
| US20020098090A1 (en) * | 1999-03-22 | 2002-07-25 | David Muhs | Pump system with vacuum source |
| US20020139738A1 (en) * | 2001-01-31 | 2002-10-03 | Kabushiki Kaisha Toshiba | Filtering apparatus, back wash method therefor, filtering device and power plant |
| US20030118503A1 (en) * | 2000-03-17 | 2003-06-26 | Chunmin Pu | Advanced control strategies for chlorine dioxide generating processes |
| US7014779B1 (en) * | 2003-03-19 | 2006-03-21 | Kirchner Edward C | Vacuum separation, transport and collection system for immiscible liquids |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3937831B2 (en) * | 2001-12-18 | 2007-06-27 | 富士ゼロックス株式会社 | Power supply device and image forming apparatus using the same |
-
2006
- 2006-04-13 CA CA2543385A patent/CA2543385C/en active Active
- 2006-04-13 US US11/402,946 patent/US7651865B2/en active Active
-
2009
- 2009-11-02 US US12/588,897 patent/US20100047127A1/en not_active Abandoned
Patent Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3637079A (en) * | 1967-07-12 | 1972-01-25 | Filtrox Maschinenbau Ag | Filter and method of cleaning the filter |
| US5104553A (en) * | 1987-12-23 | 1992-04-14 | Oerlikon-Contraves Ag | Apparatus for filtering a reagent |
| US6134952A (en) * | 1997-09-18 | 2000-10-24 | Alberta Research Council Inc. | Dissolved solid analyzer |
| US20020098090A1 (en) * | 1999-03-22 | 2002-07-25 | David Muhs | Pump system with vacuum source |
| US20030118503A1 (en) * | 2000-03-17 | 2003-06-26 | Chunmin Pu | Advanced control strategies for chlorine dioxide generating processes |
| US20020139738A1 (en) * | 2001-01-31 | 2002-10-03 | Kabushiki Kaisha Toshiba | Filtering apparatus, back wash method therefor, filtering device and power plant |
| US7014779B1 (en) * | 2003-03-19 | 2006-03-21 | Kirchner Edward C | Vacuum separation, transport and collection system for immiscible liquids |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103630427A (en) * | 2013-11-25 | 2014-03-12 | 北京矿冶研究总院 | Automatic ore pulp filtering and sampling device |
Also Published As
| Publication number | Publication date |
|---|---|
| US7651865B2 (en) | 2010-01-26 |
| CA2543385C (en) | 2015-02-03 |
| US20060251560A1 (en) | 2006-11-09 |
| CA2543385A1 (en) | 2006-10-14 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP1278910A1 (en) | Method and apparatus for regulating a peroxide bleaching process | |
| EP0469437B1 (en) | Method of and apparatus for preparing calibration gas | |
| US4731176A (en) | Control system for froth flotation processes | |
| JPS63237757A (en) | Fermentation control of unrefined soy sauce and device therefor | |
| US20100047127A1 (en) | Conditioning slurry samples for quantitative instrumental analysis | |
| US7871194B2 (en) | Dilution apparatus and method | |
| CN207051141U (en) | The multi-functional on-line analysis system of wet desulphurization slurry | |
| CN111366681B (en) | Intelligent online analysis system for oxygen concentration of centrifugal machine | |
| EP2437054A1 (en) | Method for analyzing aqueous ammonium carbamate solution, and method for operating unreacted gas-absorption tank | |
| EP2958668B1 (en) | Multi-purpose machine for preparing, measuring out and controlling process additives and adjuvants in wine production | |
| KR101547167B1 (en) | On-line monitoring system for metal included in gas sample | |
| NO313218B1 (en) | Method and apparatus for sampling in a material mixture | |
| CN219957092U (en) | Alkali liquor absorption sample preparation device, detection sample preparation device and detection system | |
| CN112748190A (en) | Interface system and corresponding method | |
| CN219348615U (en) | Quick detection test device for chloride ions in chemical fertilizer | |
| CN214528145U (en) | On-line analysis equipment for alkalinity of working solution in preparation of hydrogen peroxide by anthraquinone process | |
| RU2208783C1 (en) | Facility to prepare testing gas mixtures | |
| US20240209465A1 (en) | Process for producing thin juice for the production of sugar, process for producing sugar and sugar production plant | |
| CN210269762U (en) | Automatic detection device for gas mercury detector | |
| CN110411974B (en) | Device for detecting hydrocarbon and hydrogen in circulating water | |
| Casas et al. | SFE kinetics of bioactive compounds from Helianthus annuus L. | |
| KR200168089Y1 (en) | A reaction gas analysis ststem for fermentation tube | |
| US5023803A (en) | Process to control the addition of carbonate to electrolytic cell brine systems | |
| CN223006035U (en) | A monitoring device for the synthesis and production of hydrosulfur powder | |
| CN104897606A (en) | Rapid analysis method of methylhydrazine reaction process stream |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| STCB | Information on status: application discontinuation |
Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION |