Water Vapour
Measurement in Process Gases
The Trials & Tribulations of Moisture Measurement
In our everyday
lives we encounter situations where industrial processes can
pollute and contaminate our drinking water and/or bodies of water
which are sources of food and recreation. However in an ironic
role reversal, in many industrial processes water can be the
contaminant. Removing this water (typically in vapor form) can
be vital to the quality of the process/product, but can also
be very costly.
Water vapor is the third largest component of our atmosphere
(after Nitrogen and Oxygen); and because it is a small polar
molecule it is able to get even into places that otherwise seem
well sealed.
If water vapor
is a contaminant in a process, it must be removed. But since
it is costly to remove it (the lower the desired level the costlier
it gets) it becomes essential to determine accurately and quickly
the water vapor content of a particular process. In addition,
alarms for excessive water vapor content are required to prevent
the decline of product quality. Thus some of us get tasked with
the challenge of making that measurement and must take into account
many considerations. In a short article we can't cover all of
them or even explore the details of the ones we do mention, but
we can become aware of what to research elsewhere. Following
are some important points:
1. Like most
endeavors our expectations must be in line with reality. It is
important to cast off hopes that this measurement is like the
measurement of temperature or pressure. Let me assure you it
is not: in price for the equipment, in speed of response, and
especially in the uncertainty of the measurement. Equipment for
measuring water vapor in gas is much more like a laboratory analyzer
than like a temperature or pressure transmitter. Yet we have
to make the measurement in a real process and deal with field
conditions. Choosing the most appropriate technology for the
particular measurement is not a trivial task and it is further
confused by a marketplace littered with unrealistic claims.
2. The terminology
of water vapor measurement is wide-ranging. The proper terminology
for water vapor is "Humidity", however commonly many
refer to it as "Moisture" (which actually should mean
liquid water). Traditionally "Humidity" references
imply higher contents of water vapor such as found in the atmosphere
(in the many 1000's of ppmv) and some use "Trace Moisture"
to mean very low amount of water vapor (in the ppm or ppb levels).
I will continue to use water vapor in hopes of avoiding confusion.
I have encountered the following references in water vapor measurement
discussions - some of which refer to the technology used or the
units of measure: Moisture Analyzer, Dewpoint Analyzer, Dew Point
Meter, Dew pointer, Hygrometer, Chilled Mirror, Humidity Meter,
Hygrometrics, Phychometrics, These are not necessarily all interchangeable.
3. The units
of measure are commonly determined by the particular industry
and its historical measurements. Some of the units of measure
one may encounter are:
a. Partial water vapor pressure - uB or mB or mmHg or Pascal
etc
b. relative humidity - RH%
c. vapor concentration (density) - lbs of water per million standard
cubic feet (lbs/mmscf), or g/m3
d. Dew point or frost point temperature - °C or °F etc
e. ratio by volume - ppmv or ppbv
f. ratio by mass (more commonly used for solids or liquids) -
ppmw
Understanding
these units of measure is intricate and making accurate conversions
challenging, in addition some conversions require knowing the
pressure while others the temperature of the gas. There are several
formulas for converting units as well as several enhancement
factors for the medium and none of them produce the same results,
even though they are close enough for most practical applications
the differences can be a source of confusion.
4. Some have
preconceived notions of what the water vapor content should be
in their process, or how well the process is sealed. One must
keep an open mind that these notions could be erroneous. Water
molecules will travel against the flow (and pressure gradient)
of gas from the exhaust of a process, water molecules will permeate
to some degree many if not most materials and even some metals,
water molecules will tenaciously cling to almost any surface
for a prolonged time. One can see that these facts in conjunction
with the possible 20,000 ppmv content of water vapor in the atmosphere
could cause your process to have different water vapor content
than you think.
5. Strategically
positioning the measurement equipment can have significant affect
on the process if something goes wrong. Should it be positioned
near the source of the dry gas in order to provide an early warning
of a failure in the supply system; or should it be near the end-use
point as to also detect leaks in the distribution system. To
measure in-situ or extractive? To measure at pressure or atmospheric?
All of these considerations will have an impact on the quality
and long-term reliability of your measurement.
6. There are
many other important considerations but I will mention only one
more: Carefully consider how often to re-calibrate the equipment.
A general rule of thumb is to initially re-calibrate in one year,
ask the calibration lab for as-is-data which can be used to determine
when should you calibrate again. Consider if the process will
have to be interrupted to facilitate calibration. When choosing
a vendor inquire about the calibration turnaround time and traceability.
I will leave
you with an old chemistry class reminder, water vapor is a gas
and it behaves according to Dalton's Law of partial pressures;
it will permeate into sealed environments if the partial water
vapor pressure in the atmosphere is greater than in the sealed
environment - even though the sealed environment is at a total
pressure much greater than atmospheric. For many of us this is
somewhat counter intuitive but we cannot let intuition override
science.
To determine the content of water vapor, you must be determined.
Happy Measuring
This article has been kindly
supplied by :
Author: Bedros
Bedrossian
Phymetrix Inc.
For further information please visit www.Phymetrix.com
Contact: Deborah@Phymetrix.com
28C Industrial blvd
Medford, New York 11763
631-903-2547