Guided Wave Application Note: A Word (or Two) About Online NIR Water Measurements in Liquid Samples (White Paper)
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Process Analytical Systems
Application Note:
A Word (or Two) About Online NIR Water Measurements in
Liquid Samples
Introduction
Water is perhaps the most common measurement made in the
near-infrared (NIR). This is due to its strong effect on product
properties and chemical reactivity of the starting materials. From
an analytical perspective, water is easy to analyze due to its relatively strong signal compared to the hydrocarbon background.
Moreover, because water is commonly analyzed with a single
wavelength, photometers are the instrument of choice. The
purpose of this application note is to show you how we arrive at
recommending a system, that is, a photometer with the proper
wavelengths and a fiber optic probe with an appropriate sample
path length.
Factors to Consider
(1) background hydrocarbon spectral characteristics, (2) concentration range of water and desired analytical precision, (3) potential interference from hydroxyl, (4) sample temperature variations,
and (5) sample clarity. These considerations affect the choice
(and price) of the appropriate photometer and probe system.
Analytical Goals
(1) provide maximum sensitivity, (2) select wavelength(s) to keep
the absorbance below 1.2 Absorbance Units (AU), (3) minimize
interferences due to background hydrocarbon variations and sample temperature changes, and (4) use an optical path of >1 mm
in the fiber optic probe for ease of cleaning and minimal entrapment of bubbles and particles.
Rule-of-Thumb
The 1900 nm region is generally used for <1% water. In a
ClearView® db photometer, a precision near ±20 ppm can be
achieved. The 1400 nm region is used for >1% water and a precision of near ±100 ppm is attainable.
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For process analyzers, long-term (monthly) photometric drift is
the most meaningful measure of “precision”. In ClearVIew db
this is typically <500μAU.
OH vs. H2O
The 1400 nm region contains the 1st overtone of the O-H stretch
in water and hydroxyl, as shown above for water and ethylene
glycol. Mixtures of water and alcohols, therefore, have overlapping features due to water and hydroxyl in this region. Water
additionally has a unique peak near 1900 nm due to a combination of its O-H stretch and its H-O-H bending. The large peak
near 2100 nm is a combination of O-H and C-H in the glycol.
Notice that this pure glycol lacks an appreciable peak near 1900
nm where molecular water absorbs. With equivalent optical
paths, you can see how much stronger water is compared to the
C-H features.
Precision
The water peak at 1900 nm is about five times as large as its
peak at 1430 nm. For example, 1 mAU in the 1900 nm region
for n-propanol corresponds to about 20 ppm water for a 1 cm
optical path, and about 90 ppm near 1430 nm. For water in
methyl-isobutyl ketone (MIBK) or tetrahydrofuran (THF) these
values are about 12 and 85 ppm/mAU, respectively. By doubling
the optical path to 2 cm, if possible, the precision is also doubled. Take a conservative 3s drift of 1.5 mAU for a ClearView db,
and we arrive at ±20 ppm at 1900 nm and ±125 ppm at 1430
nm with a 1 cm probe.
Application Note:
A Word (or Two) About Online NIR Water Measurements in
Liquid Samples
Spectral Background and Path Length
The absorbance from an organic liquid near 1900 nm is highly
variable. CCl4 has no appreciable absorbance in this region.
Optical paths from 10 to 20 cm can be used to achieve <1
ppm precision. In contrast, many alcohols have significant
absorbance. For example, ethylene glycol at 1900 nm has
about 1.4 AU for a 1 cm optical path. Therefore, we could use
a 5 mm optical path in a fiber optic probe to provide a 0.7 AU
“baseline” absorbance in ethylene glycol. At 5 mm, the precision for water in ethylene glycol is about 24 ppm/mAU, so 1%
water would add about 0.4 AU to the 0.7 AU resulting in an
absorbance near 1.1 AU. You can see that adding >1% water
to ethylene glycol, even in a 5 mm probe, would lead to an absorbance larger than our 1.2 AU desired limit. Thus, 2% water
in ethylene glycol is measured with a shorter path, such as 2 or
3 mm, with some sacrifice in precision to achieve the greater
concentration range.
spectrum between the water and “reference” wavelengths.
Since we are already quantifying mAU changes at the water
peak, it does not take much of a “tilt” to significantly impair a
water calibration. The greater the wavelength difference, the
more the effect, such as at 1900 nm. We can always choose a
“reference” wavelength on either side of the 1900 nm water to
minimize this effect, but it is still important to install particle filters and sample temperature control. We use the voltage from
the detector at the “reference” wavelength to indicate sample
clarity. It can be sent to your DCS as a 4-20 mA analog output
and monitored continuously.
Conclusions
By considering the issues raised above, we can provide you
with a cost-effective solution to obtain the desired sensitivity for
water over the concentration range of interest in most organic
liquids.
Temperature Effects
Figure 2
The top of the water peak near 1430 nm is shown in Figure 2.
These spectra represent water at different temperatures from
30 to 60 ºC. They intersect at 1430 nm. There is an analogous
intersection on the 1900 nm peak shown on the previous page.
This means that different temperatures have different calibration
curves. In some of our studies of percent water in acids in the
1400 nm region, a 1 ºC change can lead to a 0.1% (1000 ppm)
change in the calculated water concentration. There are several
methods to minimize sample temperature effects. The piping in
a side stream can be heat traced or the wavelength at the spectral intersection point can be used for the calibration. Perhaps
the most common solution is to measure the sample temperature with an RTD sensor or thermocouple near the probe and
send the signal back to a the ClearView® db photometer. The
software is equipped to correct water calibrations for sample
temperature variations.
ClearView db Configurations
Sample Clarity
A photometer computes the absorbance between the water
wavelength and a “reference” wavelength (= -log Water/Reference) and converts that into water concentration. The “reference” wavelength is typically chosen in a “valley” which has
little absorbance change, such as 1300 nm. The presence of
light scattering entities entrained in the sample stream, such as
bubbles, particles or immiscible phases, can “tilt” the entire
Process Analytical Systems
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