If other species (Different Gas Components) of gas present in the sample do not absorb any of the light wavelengths absorbed by the one gas we’re interested in measuring, the selectivity of a Luft detector will be total: the gas-filled detector will only respond to the presence of the gas we are interested in. Usually, though, process applications are not this simple. In most applications, the interfering gases have absorption spectra overlapping portions of the interest-gas spectrum. This means changes in interference gas concentration will be sensed by the detector (though not as strongly as changes in the concentration of the gas of interest) because part of the light spectrum absorbed by the interfering gas(es) will have a heating effect on the pure gas inside the detector. An example of overlapping absorption spectra is found with the combination of carbon dioxide and acetylene gases:
As you can see, there is some common absorption between these two gas species toward the right-hand side of the scale, around 700 cm−1 (approximately 14000 nm wavelength). An NDIR analyzer equipped with a Luft detector filled with 100% of carbon dioxide gas will respond strongly to concentrations of carbon dioxide gas in the sample chamber, and weakly to concentrations of acetylene gas in the sample chamber. Since acetylene does absorb some of the infrared light wavelengths absorbed by carbon dioxide, acetylene gas has the potential to affect the Luft detector and make the analyzer “think” it is measuring slightly more carbon dioxide gas than it actually is.
One more addition to our NDIR instrument helps eliminate this problem: we add two more gas cells in the path of the light beams, each one filled with 100% concentrations of the interfering gas. For this particular example, we would fill each filter cell with a 100% concentration of acetylene gas, and the Luft detector cell with a 100% concentration of carbon dioxide gas:
These filter cells purge the light of those wavelengths normally absorbed by the interfering gas (acetylene) inside the sample cell. As a result, the presence of that interfering gas in the sample cell will have negligible effect on the light exiting the sample cell, because those wavelengths have already been severely attenuated by the filter cells. If the filter cells happened to be 100% effective in filtering all wavelengths specific to the interfering gas, there would be absolutely none of the interfering gas’s specific wavelengths of light left to be absorbed inside the sample cell, and therefore the interfering gas would have absolutely no effect on the detector’s response. In other words, by filtering out all the light wavelengths absorbed by the interfering gas inside the filter cells, the presence of that same gas in the sample cell will have no effect on the detector, and therefore it can no longer interfere with the measurement of our gas of interest.
So long as our gas of interest exhibits absorption wavelengths not shared by the interfering gas (i.e. wavelengths of light unique to the gas of interest alone), these wavelengths will still be able to pass through the filter cells and into the sample cell where they will change intensity as the gas of interest varies in concentration. Thus, the detector now only responds to the gas of interest (carbon dioxide), and not to the interfering gas (acetylene).
As effective as this filtering technique is, it has the limitation of only working for one interfering gas at a time. If multiple interfering gases exist in the sample stream, we must use multiple filter cells to block those light wavelengths.
A photograph showing a dual-beam NDIR analyzer appears here:
What looks like a single gold-colored gas cell is actually two cells (a divider separating the tube lengthwise into two chambers), one for the sample gas and the other for reference. Blackcolored hoses pass sample gas through the bottom half of the tube, while the top half is filled with nitrogen gas (the tube connections capped and sealed with black-colored plastic). The light source and chopper assembly appears on the left-hand side of the tube, while the detector resides on the right-hand side.
In this particular instrument (a Rosemount Analytical model X-STREAM X2), the chopper wheel is driven by a stepper motor:
The head of the infrared light source appears just to the right of the chopper wheel motor.
The detector used in the X-STREAM NDIR analyzer is a modern variant of the Luft detector, with a micro-flow sensing element detecting pulses of gas flow between two chambers. In this particular analyzer the detector chambers are filled with carbon monoxide (CO) gas, to sensitize it to that species:
This instrument’s maximum detection range happens to be 0 to 1000 ppm of carbon monoxide, with the ability to turn down to a range of 0 to 400 ppm.
Also Read : Absorption Type Optical Analyzer
- Luft detector Principle
- Infrared Non Dispersive CO2 Analyzer Working Principle
- Gas Filter Correlation (GFC) Spectroscopy
- Single-beam Non-dispersive Analyzer
- Non-Dispersive Analyzers
- NDIR Gas Analyser Working Principle
- H & B Gas Analyzer Principle and Calibration Procedure
- TOC Analyzer Working Principle
- Carbon Monoxide Questions & Answers
- Pulsed Fluorescence SO2, H2S, CS Analyzer Working Principle