Use of detection techniques for contaminant and corrosion control in industrial processes
Industrial fluids may be monitored at the site of each industrial fluid by introducing a sample of the industrial fluid into a device employing a detection technique for detecting at least one composition within the sample. The detection technique may be or include surface enhanced Raman scattering (SERS), mass spectrometry (MS), nuclear magnetic resonance (NMR), ultraviolet light (UV) spectroscopy, UV spectrophotometry, indirect UV spectroscopy, contactless conductivity, laser induced fluorescence, and combinations thereof. In one non-limiting embodiment, a separation technique may be applied to the sample prior to the introduction of the sample into the device for detecting the composition.
1. A method for monitoring at least one industrial fluid comprising:
a. introducing a sample of the at least one industrial fluid into a device employing a detection technique selected from the group consisting of surface enhanced Raman scattering (SERS), indirect UV spectroscopy, contactless conductivity, and combinations thereof; wherein the industrial fluid is selected from the group consisting of a refinery fluid, a production fluid, cooling water, process water, drilling fluids, completion fluids, production fluids, crude oil, feed streams to desalting units, outflow from desalting units, refinery heat transfer fluids, gas scrubber fluids, refinery unit feed streams, refinery intermediate streams, finished product streams, and combinations thereof; and
b. detecting at least one composition within the sample of the at least one industrial fluid, wherein the at least one composition is monoethanolamine (MEA) in the presence of other compounds; and
wherein the method occurs in an amount of time less than about 24 hours.
2. The method of claim 1 , further comprising conditioning the sample prior to introducing the sample of the at least one industrial fluid into the device, wherein the conditioning is a method selected from the group consisting of filtration, pH adjustment, chemical labeling, a separation technique, solid-phase extraction, adding a background electrolyte (BGE) to the sample, adding a complexing agent to the sample, adding peroxide to the sample, adding a chelant to the sample, applying chelating resins to the sample, and combinations thereof.
3. The method of claim 2 , wherein the conditioning is a separation technique selected from the group consisting of ion chromatography (IC), high performance liquid chromatography (HPLC), capillary electrochromatography (CEC); electrokinetic chromatography (EKC), affinity capillary electrophoresis (ACE), non-aqueous capillary electrophoresis (NACE), capillary electrophoresis (CE), capillary zone electrophoresis (CZE), gradient elution moving boundary electrophoresis (GEMBE), capillary isotachophoresis (CITP), capillary isoelectric focusing (CIEF), and combinations thereof.
4. The method of claim 1 , wherein the at least one composition within the at least one industrial fluid is quantified in an amount greater than about 10 ppb.
5. The method of claim 1 further comprising altering or controlling at least one element of a process after detecting the at least one composition.
6. The method of claim 1 , wherein the amount of the sample introduced into the device ranges from about 1 μL to about 250 μL.
7. The method of claim 1 , wherein the detecting the at least one composition occurs in an amount of time ranging from about 30 seconds to about 5 hours.
8. A method for monitoring at least one industrial fluid comprising:
a. performing a separation technique on a sample of the at least one industrial fluid to form a separated sample; wherein the separation technique is selected from the group consisting of ion chromatography (IC), high performance liquid chromatography (HPLC), capillary electrochromatography (CEC), electrokinetic chromatography (EKC), affinity capillary electrophoresis (ACE), non-aqueous capillary electrophoresis (NACE), capillary electrophoresis (CE), capillary zone electrophoresis (CZE), gradient elution moving boundary electrophoresis (GEMBE), capillary isotachophoresis (CITP), capillary isoelectric focusing (CIEF), and combinations thereof;
b. introducing the separated sample into a device employing a detection technique selected from the group consisting of surface enhanced Raman scattering (SERS), nuclear magnetic resonance (NMR), indirect UV spectroscopy, contactless conductivity, and combinations thereof; and wherein the industrial fluid is selected from the group consisting of a refinery fluid, a production fluid, cooling water, process water, drilling fluids, completion fluids, production fluids, crude oil, feed streams to desalting units, outflow from desalting units, refinery heat transfer fluids, gas scrubber fluids, refinery unit feed streams, refinery intermediate streams, finished product streams, and combinations thereof;
c. detecting at least one composition within the sample, wherein the at least one composition is monoethanolamine (MEA) in the presence of other compounds; and
wherein the method occurs in an amount of time less than about 24 hours.
9. The method of claim 8 , wherein the sample is conditioned prior to a step selected from the group consisting of performing the separation technique, introducing the sample into the device, and prior to both.
10. The method of claim 9 , wherein the sample is conditioned by a method selected from the group consisting of filtration, pH adjustment, chemical labeling, solid-phase extraction, adding background electrolyte (BGE) to the sample, adding a complexing agent to the sample, adding peroxide to the sample, adding a chelant to the sample, applying chelating resins to the sample, and combinations thereof.
11. The method of claim 8 , wherein the at least one composition within the at least one industrial fluid is quantified in an amount greater than about 10 ppb.
12. The method of claim 8 , wherein the amount of the sample introduced into the device ranges from about 1 μL to about 250 μL.
13. The method of claim 8 further comprising altering or controlling at least one element of a process after detecting the at least one composition.
14. The method of claim 8 , wherein the industrial fluid is selected from the group consisting of an aqueous fluid, a non-aqueous fluid, and combinations thereof.
15. The method of claim 8 , wherein the detecting the at least one composition occurs in an amount of time ranging from about 30 seconds to about 5 hours.
16. A method for monitoring at least one industrial fluid comprising:
a. conditioning a sample of the at least one industrial fluid by capillary electrophoresis (CE) prior to:
b. introducing the sample into a device employing the detection technique of surface enhanced Raman scattering (SERS) or nuclear magnetic resonance (NMR); wherein the industrial fluid is selected from the group consisting of a refinery fluid, a production fluid, cooling water, process water, drilling fluids, completion fluids, production fluids, crude oil, feed streams to desalting units, outflow from desalting units, refinery heat transfer fluids, gas scrubber fluids, refinery unit feed streams, refinery intermediate streams, finished product streams, and combinations thereof; and
c. detecting at least one composition within the sample of the at least one industrial fluid, wherein the at least one composition is monoethanolamine (MEA) in the presence of other compounds; and
wherein the method occurs in an amount of time less than about 24 hours.