OHAUS Labtex Ingeniously Practical User Guide
- June 9, 2024
- Ohaus
Table of Contents
- Introduction to Moisture Content and Overview of Measuring Techniques
- Installation and Initial Setup
- Moisture Determination Using an MB Series Moisture Analyzer
- Getting Started: Sample Consideration and Method Development
- Cleaning and Maintenance
- Appendix A Sample Methods
- Troubleshooting
- References
- Read User Manual Online (PDF format)
- Download This Manual (PDF format)
Labtex Ingeniously Practical
User Guide A Guide to
Moisture Content Analysis
Labtex Ingeniously Practical
Introduction to Moisture Content and Overview of Measuring Techniques
Definition of Moisture Content
Water is essential to life; it plays a critical role in the physical and
chemical functions of our bodies, the food we eat, and the materials that
surround us In many industries it is important–if not critical–to measure the
water content of substances in order to assess quality, adjust manufacturing
processes, and ensure that products meet regulations and guidelines The amount
of available water dictates the shelf life and stability of many systems; for
example, the presence of water in food greatly impacts its susceptibility to
chemical, enzymatic, and microbial activity
Water content is also important for the processing and handling of:
- Cosmetics
- Pharmaceuticals
- Food
- Personal care products
- Pulp and paper products
- Specialty chemicals
Measuring the amount of water contained in certain materials can be very
difficult due to the complexity of the water molecule and its strong
intermolecular bonding capabilities In most cases, measurement of water is
better defined as the measurement of moisture content, defined as the mass of
water per unit mass of dry material.
The MB Series of moisture analyzers (or moisture balances) from OHAUS measure
moisture thermogravimetrically Thermogravimetric moisture analysis defines
moisture as the loss of mass observed when the sample is heated and is based,
in theory, on the vaporization of water during the drying process; this
measurement does not distinguish weight loss of water from loss of volatile
components or sample decomposition For this reason, moisture content as
measured by thermogravimetric techniques includes all substances which
vaporize when heating a sample and are measured as weight loss during the
heating process. Therefore, we use the term “moisture content” rather than
“water content” when using a thermogravimetric device.
What Is Thermogravimetric Moisture Analysis?
Moisture content influences the weight, density, viscosity, refractive index,
and electrical conductivity of a material Methods for testing moisture content
tend to exploit one or more of these physical or chemical properties Direct
measurements address the presence of water itself, either through its removal
or through chemical interaction The use of a thermogravimetric moisture
analyzer is a way to directly measure the moisture content of a sample by
using the loss on drying (LOD) technique LOD measures the weight of a sample
before and after a drying procedure and uses the weight delta to determine the
percentage of moisture as the weight removed by the drying process in
comparison to the initial weight of the sample.
Typically this process is done in a drying oven with a balance to determine
the initial and final weight of the sample and using a simple mathematical
calculation to determine the moisture content ([initial weight end
weight]/initial weight) This process typically takes several hours to complete
and is vulnerable to user error A moisture analyzer works on the same
principle, but is an automated system that employs a microprocessor-controlled
heating element and an analyzer all in one device; by using such a device, the
moisture content of a sample can be measured in minutes rather than hours
Halogen vs. Metal Heating
Thermogravimetric moisture analyzers efficiently dry a sample by transferring
energy by both radiation (the transmission of energy in the form of waves or
particles through a medium–in this case, the sample) and convection (heat
transfer by mass motion) In comparison, a conventional drying oven uses mostly
convection to dry a sample Both metal and halogen heating elements radiate
energy in the infrared spectrum (Both methods are employed in the OHAUS MB
Series ).
Infrared (IR) radiation is part of the electromagnetic spectrum, falling
between microwave energy and visible light Infrared waves include thermal
radiation and have the wavelength frequency range from 0 75 micrometers (long
wavelength limit of visible red light) to 1 5 micrometers (borders on
microwaves) Infrared energy is not visible to the human eye The red light
often associated with infrared heating is actually reflected red light from
the visible spectrum.
Some moisture analyzers utilize a metal heating element, which is simply a
low-resistance piece of metal which converts electricity into heat Such
heaters are ideal for an environment (such as food processing) where the
presence of glass components are prohibited due to regulatory or safety
concerns Metal heaters are not ideal as they have a very large thermal mass
and take significantly longer to heat up than halogen heaters, and are thereby
harder to control and do not provide optimum repeatability in a moisture
analyzer Halogen radiators have a tungsten heating element contained in a
compact glass tube filled with halogen gas to preserve the tungsten element
The halogen radiator emits infrared radiation in the short wavelength range of
0 751 5 micrometers The compact nature of the halogen radiator improves the
heating/cooling response time, shortening the time for the heating unit to
reach full heating power and ultimately shortening time requirements to
complete sample drying; it also allows finer control during the heating
process.
Fast heating to minimize testing time.
Infrared halogen heating technology begins drying each sample in seconds and
performs up to 40% faster than traditional infrared methods, for higher
throughput and a more efficient work day.
Installation and Initial Setup
It is imperative that the moisture analyzer unit is correctly installed in
order to ensure high repeatability and the best possible results Because
environmental changes can adversely affect the result of a moisture
measurement, the moisture analyzer should typically be placed in a location
where environmental factors (temperature, humidity, vibration, etc ) are as
stable as possible It is not only important to ensure that the temperature is
stable during a measurement, but also that the moisture analyzer is located in
an environment similar to that when the device was calibrated. If the
operating conditions change, the device must be recalibrated using a
temperature adjustment kit to obtain the best possible results. Refer to your
operating manual for instructions on how to perform a temperature adjustment
on your MB Series moisture analyzer.
In the next section, we’ll explore the factors that should be considered when
placing your moisture analyzer.
Selecting a Location
Physical Location
As with any balance, a moisture analyzer should be placed on a solid table or
workbench that is free of vibration The surface should be stable enough that
no vibrations are registered as a change in weight when it is pushed on, or
when walking around the area Please note that the unit contains a fan that
circulates ambient air through a chamber within the device to help ensure a
constant temperature at the weighing cell when heating To ensure that this fan
functions properly, the moisture analyzer should be placed in an open area and
not directly against a wall.
For extremely sensitive samples or for cases where sensitivity in reading is
critical, consider placing the analyzer in an environmental chamber where
temperature and humidity are tightly controlled.
Temperature
Changing temperatures and cold-start conditions (the starting state of the
moisture analyzer after it has not been used for a period of time) may
adversely affect your results Ideally, an operating temperature of 20°C should
be maintained Once the device is installed, the temperature should remain
constant and the device should not be placed in close proximity to other
objects (including windows) that emit heat The operating temperature should
never exceed the limits specified in the operating manual or data sheet
Humidity
It is also important to avoid rapid changes in humidity, which can affect the
weighing cell and cause it to drift, potentially leading to an inaccurate
measurement result The relative humidity should be approximately 50% and the
ambient relative humidity should never exceed the limits specified in the
operating manual or data sheet Once the device is installed, the ambient
relative humidity should remain constant
Air Currents
As with any balance, the moisture analyzer should be placed in a location free
of air currents This includes drafts caused by open windows or HVAC systems
Initial Setup
Turning On
Once the moisture analyzer has been set up for use, it is best practice to
keep the device plugged in While the display may be turned off to conserve
power, the weighing cell should be powered constantly to ensure that it is
always ready for measurement When the analyzer has been plugged in for the
first time, allow it to warm up for 3 hours before initial use
Leveling
It is important to level the moisture analyzer to ensure best weighing
accuracy To level the analyzer, rotate the leveling feet until the level
bubble is in the correct position Consult your device’s operating manual for
additional information about how to properly level your moisture analyzer
Adjusting
The OHAUS MB Series of moisture analyzers arrive adjusted and ready to use in
optimum environments It is recommended to re-adjust the analyzer by performing
a weight and temperature adjustment before it is first used and if any changes
are made to the ambient conditions (including moving it to a new location) in
order to compensate for changes that may affect how much energy is delivered
to the sample surface It is also recommended to periodically adjust the
moisture based on use to compensate for any buildup of substances on interior
surfaces (see the cleaning and maintenance section of this document for
additional details)
Moisture Determination Using an MB Series Moisture Analyzer
Please note: Although this section refers specifically to the OHAUS MB120
moisture analyzer (and some features may not be available on other models),
the principles described here can be applied to any thermogravimetric moisture
analyzer.
The MB Series of moisture analyzers from OHAUS are based on halogen radiator
technology (with the exception of the MB23, which utilizes a metal heating
element) These instruments can be used to measure the moisture content of a
wide array of materials.
What Is a Method?
A method is a set of parameters that defines how a sample is dried A method
consists of a drying program, temperature(s), a shut-off criterion, and other
parameters that define how the results are displayed (e g , units of measure)
The user can determine the best method to dry a sample to produce the required
result
Accuracy vs. Precision
Accuracy is how close a measured value is to an actual or true value Precision
is how close measured values are to each other, commonly measured by the
standard deviation of a set of values It is important to note that the goal of
a moisture analyzer is to be precise–so that multiple samples measured under
the same conditions produce a set of results with very little variance The
user must select a method and prepare the sample in a way to ensure
accuracy.
In order to illustrate this concept, consider the example of baking cookies If
the dough is prepared in the same way and applied in homogeneous and
consistent chunks on a baking pan, it is possible that the oven may undercook
(if the temperature is too low or baking time is too short) or burn (if the
temperature is too high or baking time is too long) the dough However, if the
dough is prepared consistently and baked using the optimum temperature and
time, the cookies should come out exactly the same each time Likewise, if the
user of a thermogravimetric instrument provides the correct inputs, the
results should be of very low variance
Method Parameters
Drying Temperature
The MB Series of moisture analyzers (depending on model) provides a wide range
of drying temperatures While temperatures from 40°C230°C can be achieved in a
drying application, most samples are measured in the range of 100°C140°C
Drying Profiles
Moisture content (MC) is greatly influenced by the drying temperature used to
drive off the moisture Excessive heating may result in a high percentage MC
reading due to sample decomposition or changes in chemical structure Besides
giving artificially high readings, results are very difficult to reproduce in
tests when the drying profile is too harsh Conversely, lower heating levels
may preserve sample integrity but prolong the drying process, making the test
unrealistic for process use
The MB Series of moisture analyzers offers a series of drying programs that
allows users to customize the sample drying profile By customizing the drying
program, moisture measurements can be optimized to enhance drying conditions
and shorten runtime while minimizing sample decomposition or change in
chemical structure, ultimately improving testing accuracy and reproducibility
The four basic temperature profiles–standard, fast, step, and ramp–can be
customized by specifying a target temperature(s)
Standard
The standard drying profile is the most common and is sufficient for most
samples In this drying profile the target temperature is reached and sustained
until the end of the measurement.
Figure 1. Standard drying profile
Fast
The fast drying profile is suitable for samples with higher moisture content,
as it relies on available moisture to prevent charring of the sample In this
drying profile, the target temperature is exceeded by 40% for the first 3
minutes, then reverts to the target temperature which is sustained until the
end of the measurement.
Figure 2. Fast drying profile
Step
The step drying profile allows for multiple temperatures to be sustained for
defined periods of time, allowing for tighter control of the drying
temperature This profile can be useful for samples in which a lower
temperature is first used to dry and measure surface moisture and a higher
temperature to release and measure bound moisture Alternatively, a higher
temperature may be used first to burn off volatile solvents, then a lower
temperature(s) can be used to measure water content
Figure 3. Step drying profile
Ramp
The gentle ramp drying profile allows the user to ramp up the temperature
slowly over a period of time This can be useful to dry a substance with a high
sugar content, where a slow temperature ramp will increasingly allow bound
water to be evaporated before a caramelized layer is formed, trapping bound
water underneath.
Figure 4.
Ramp drying profile
Shut-Off Criteria
A shut-off criterion defines when the moisture analyzer stops heating and
considers a measurement complete This can be done either manually or via
several built-in options to ensure accurate, reproducible results When and how
the instrument terminates a heating profile can be programmed according to
runtime or according to steady-state weight conditions The available switch-
off criteria for the MB Series are defined as:
-
Manual The user defines end of run and shuts off instrument manually
-
Timed Instrument shuts off automatically at a preset time during analysis (e g , 10 minutes)
-
Auto The instrument automatically shuts off based on weight loss per unit time For the built-in automatic shutoff criteria, the end of a measurement is reached when the overall change in weight observed is less than 1 milligram per period of time The available preprogrammed choices are:
A30 = < 1 mg weight loss in 30 seconds (quick-drying samples/fast measurements)
A60 = < 1 mg weight loss in 60 seconds (most sample types)
A90 = < 1 mg weight loss in 90 seconds (slow-drying samples) -
AFREE Auto-free switch-off; allows the user to define shut-off criteria according to weight loss per unit time
Sample Preparation
Sample collection and sample preparation have a great influence on moisture
readings and reproducibility Sample collection may mean obtaining samples from
the processing line at given time intervals or on a batch-to-batch basis for
any given day.
To ensure reproducible results, it is important that the test sample be a
representative, homogenous mix of the material being analyzed In many systems,
it is common for moisture content to vary throughout the material For example,
the surface and edges may contain less moisture than interior portions In
order to obtain a representative sample, the material should be homogeneously
mixed, and portions of this mix used for later testing (See Appendix, Case
Study #1 ).
The amount of sample chosen can impact the moisture reading; it is crucial
that an appropriate amount be used to obtain a meaningful reading Typically, a
sample size of 510 grams is recommended; the minimum allowed weight is 0 5
grams Small sample sizes should only be used when material is difficult to
obtain or expensive.
It is important that the sample be evenly distributed on the sample pan and
that the physical state of the material allows the absorption of IR and
dissipation of moisture Although some samples can be directly added to the
sample pan, at times the sample requires some alteration to its physical state
(e g , pulverizing or grinding) in order to enhance the drying process It is
important that the sample does not gain or lose moisture during this process
With a little care and planning, change in moisture content during sample
preparation can easily be avoided.
It is best to test the sample immediately after preparation Storing the sample
in a hermetically sealed container will also help prevent moisture migration
before and between analyses.
Sample Quantity and Distribution
Sample size is dictated by distribution needs in the sampling pan and moisture
content of the sample Depending on the moisture content, optimization of
drying conditions and reproducibility may be influenced by the amount of
sample being evaluated.
Distribution of the sample in the holding pan will also affect moisture
reading and reproducibility The sample should ideally be distributed in a
thin, even layer across the surface of the pan The sample may burn where it is
spread too thin, and may retain moisture where it is piled too thick–and both
will affect the accuracy and reproducibility of the final moisture
reading. Figure
5. Examples of good and bad sample distribution in drying pan
Use of Glass Fiber Pads
Glass fiber pads are useful media for applying liquid samples, providing an
inert, porous support Dispersing the liquid into the fiber pad decreases
sample surface tension and increases overall surface area, shortening analysis
time For very sensitive measurements or research purposes, the pads can be
retained in a desiccator to avoid affecting the moisture reading (This is not
essential for routine analysis )
Glass pads can also be used for material that is sensitive to heat or has
skin-forming properties during the drying process Using the pad as a top layer
or sandwiching the material between two pads protects the sample from IR
radiation The sample can be dried by conventional heat rather than directly
from IR radiation
Getting Started: Sample Consideration and Method Development
The OHAUS MB Series of moisture analyzers can be used to analyze a wide
variety of materials The MB Series provides a wide range of options (e g ,
temperature, drying programs, shut-off criteria) you can use to build the best
method to analyze a given substance However, creating an optimal method can be
challenging; therefore, we recommend taking sufficient time to experiment with
method development.
When designing and optimizing the testing protocol, it is important to
understand your material Consider the following three factors before getting
started:
Approximation of moisture content
- Based on information in the literature
- Calculated from starting ingredients
- Estimated by comparison to related materials
Sensitivity to heat
- Presence of volatile constituents besides water
- Presence of flammable constituents
- Combustion properties of sample
Physical state of sample
- Surface properties, enhanced IR absorption
- Even sample distribution to heat
- Enhanced thermal conductivity
- Ability to dissipate heat and moisture from surface
The most common way to develop a method for a particular substance is to
obtain a reference value, then build a method to reproduce the target value
with the shortest possible drying time To obtain a reference value, use the
conventional LOD procedure and an analyzer and drying oven Alternatively, you
may use a desiccator, Karl Fisher titrator, or other methods.
Once you have obtained a reference value, you can begin to develop an
appropriate method on a moisture analyzer We recommend preparing a sample and
drying it using a best-guess temperature, then analyzing the resulting drying
curve.
For example:
- Standard drying @ 120°C
- Shut-off criterion A60
Understanding the drying curve generated during sample drying will help to define appropriate test conditions for your sample Asymptotic drying curves are indicative of samples which reach a constant moisture value during the drying process Optimizing the temperature profile and shut-off criterion is generally simple, resulting in repeatable data.
Figure 6. Representation of asymptotic curve, steady-state weig ht
In the example shown here (Figure 7), the sample has reached a steady state
and achieved the automatic shut-off criterion If the final value achieved is
lower than the expected value, this indicates that the temperature is not high
enough to release all the bound moisture; increase the temperature and repeat
the measurement until an optimal temperature is achieved Conversely, if the
resulting value is too high, this could indicate that the sample has changed
composition (burned); decrease the temperature and repeat the measurement It
is important to visually inspect the sample to determine if burning or
charring has taken place.
In other cases, samples may never reach a constant weight throughout the
drying process, resulting in a drying profile similar to that illustrated in
Figure 8 This type of curve is indicative of a sample undergoing thermal
decomposition or continual vaporization of volatile components Optimization in
this case may require lowering the temperature profile used for drying Timed
switch-off and consistent initial sample weight also help improve
repeatability.
Figure 7. Representation of drying curve which does not reach constant
weight
In some cases, it may be necessary to determine the moisture content only
using the moisture analyzer (i e , no reference value is given or can be
measured) In these cases, method development should be done as defined above,
with the goal of achieving the fastest drying time and most repeatable results
Several measurements should be made to identify and validate a sound method
Please note that the result may not indicate the actual moisture content, but
instead serve an analog or proxy to the moisture value (i e , while the final
value is not the full and true moisture content, deviations in the actual
moisture content of a sample can be detected)
GLP/ISO Compliance of Your Moisture Analyzer
To maintain competitiveness, quality control is critical for most
companies–and a moisture analyzer is an important part of your quality control
system The OHAUS MB120 is designed to be either easily integrated into a
general quality system such as GLP/GMP, or implemented into your organization
as a standard such as ISO9000 GLP requirements and ISO standards require
traceable documentation of all adjustments/calibration procedures and tests
that are performed on a measuring instrument The weighing component of any
OHAUS moisture analyzer can be adjusted following the written procedure in the
manual and using a certified weight.
The heating or temperature measurement component of the analyzer can also be
adjusted using a procedure unique for moisture analyzers The heating element
can be adjusted following the procedure outlined in the instruction manual
This procedure can be done using a calibrated thermometer to ensure that the
moisture content is determined under identical conditions regardless of the
location.
These adjustments can be documented utilizing the product software and an
attached printer.
-MOISTURE DETERMINATION-
Halogen Moisture Analyzer
Type MB120
SNR(Drying Unit)
B550824411
SNR(Terminal)
SW(Drying Unit) ……………………….1.20
SW(Terminal) ……………………………1.01.01
Method Name …………………………….COOKIES
Drying Prog……………………………. Standard
Drying Temp …………………………….160 °C
Switch Off Free……………………..(1mg/20s)
Start Weight …………………………….1.917 g
00:00 min ……………………………………..0.00 %MC
00:30 min ………………………………….12.05 %MC
01:00 min…………………………. 27.07 %MC
01:30 min ………………………..39.49 %MC
02:00 min ………………………………51.80 %MC
02:30 min ……………………………..63.33 %MC
03:00 min…………………………………. 71.94 %MC
03:30 min……………………………….. 77.31 %MC
04:00 min …………………………….80.18 %MC
04:30 min ……………………………81.06 %MC
04:35 min …………………………..81.06 %MC
Total Time ………………………………4:37 min
End Result ……………………………..81.06 %MC
Sample ID: ……………………
Signature: ……………………
Feb 23 2016 09:35
———- END ———
Figure 8. A printout example after test completion
Cleaning and Maintenance
Keeping your moisture analyzer clean and calibrated will help to ensure that the unit operates optimally and results are consistent as possible It is important to check that all surfaces of the heating chamber are free of dust and debris from previous measurements Keep the area around the sample pan clean by removing the wind ring and emptying it when needed A mild cleaning agent is recommended to wipe down all surfaces The MB90 and MB120 analyzers allow the protective glass ring below the heating element to be removed for easy cleaning (no tools needed), so that a consistent amount of energy is transferred uniformly to the sample
Appendix A Sample Methods
Applications Table Sample Methods
The table below was compiled using the MB45 moisture analyzer. A
representative mix of samples from across the industry were evaluated for
percentage of moisture content. Sample preparation, heating programs, switch-
off criteria, and the resulting moisture content (as percentage of MC) are
defined. This table may serve as a starting reference while defining working
programs for your sample. We recommend that you optimize the program for your
specific needs.
Sample | Target Weight | Prep. Method | Heating Profile |
---|
Dry Food Ingredients
Flour| 3 gms| as is, well mixed| fast, 130ºC
Corn meal| 3 gms| as is, well mixed| fast, 130ºC
Cocoa powder| 3 gms| as is, well mixed| standard, 160ºC
Pancake mix| 3 gms| as is, well mixed| standard, 160ºC
Cake mix| 3 gms| as is, well mixed| standard, 140ºC
Powdered milk| 3 gms| as is, well mixed| fast, 80ºC
Instant coffee| 3 gms| as is, well mixed| standard, 95ºC
Sugar Syrups
Honey| 1 gm| sandwich in pads| step, 130ºC 5 min , 110ºC 3 min
Molasses| 1 gm| sandwich in pads| step, 130ºC 5 min , 110ºC 3 min
Corn syrup| 1 gm| sandwich in pads| step, 140ºC 3 min , 110ºC 6 min
Finished Baked/Fried Foods
Cake| 3 gms| uniform mix of crumb| step, 140ºC 3 min , 110ºC 4 min
Cracker| 3 gms| grind uniform crumb| fast, 80ºC
Sugar cookie| 5 gms| grind uniform crumb| fast, 95ºC
Potato chip| 3 gms| small pieces| standard, 95ºC
Roasted peanuts| 3 gms| grind, 15 sec| standard, 95ºC
Misc. Foods
Carrot| 3 gms| shredded| step, 180ºC 3min, 120ºC 3 min
Dehydrated vegetables| 2 gms| as is| rapid, 80ºC
Dried herbs| 1 gm| as is| standard, 110ºC
Snack pudding| 2 gms| sandwich between pads| step, 180ºC 3min, 120ºC 3 min
Creamy salad dressing| 3 gms| spread on glass pad| step, 180ºC 3min, 120ºC 3
min
Low-fat salad dressing| 2 gms| sandwich between pads| rapid, 130ºC
Animal Feed/Grains
Dry dog food| 5 gms| grind, 30 sec| fast, 80ºC
Pelleted pet food| 5 gms| grind, 30 sec| fast, 110ºC
Cracked corn| 5 gms| grind, 30 sec| fast, 110ºC
Rye seed| 5 gms| grind, 45 sec| fast, 110ºC
Personal Care
Liquid hand soap| 1 gm| spread thin on pad| step 180ºC 3 min , 120ºC 1 min
Bar soap| 2 gms| shaved thin into dish| standard, 110ºC
Toothpaste| 1 gm| spread thin on pad| fast, 130ºC
Skin cream| 1 gm| spread thin on pad| step, 180ºC 3 min , 120ºC 8 min
Stick deodorant| 2 gms| shaved thin into dish| standard, 110ºC
Powdered detergent| 3 gms| as is| fast, 110ºC
Misc.
Latex paint| 1 gm| sandwich between pads| fast, 170ºC
Wood glue| 1 gm| spread thin on pad| standard, 135ºC
Mortar mix| 3 gms| as is| fast, 200ºC
Potting soil mix| 3 gms| as is| fast, 200ºC
Shut-off Criteria| Time| % MC| p-value (%)
---|---|---|---
A/60| 4 min| 13 4| 0 11
A/60| 4 min| 12 5| 0 15
timed| 5 min| 7 4| 0 12
timed| 5 min| 12 4| 0 07
manual| 4 min| 5 2| 0 09
manual| 4 min| 3 7| 0 2
A/30| 5 min| 14 5| 0 06
timed| 8 min| 16 1| 0 07
timed| 8 min| 21 7| 0 48
A/30| 9 min| 21 7| 0 1
A/30| 7 min| 33 6| 0 2
A/60| 4 min| 3 7| 0 04
timed| 4 min| 5 3| 0 03
A/30| 2 min| 0 78| 0 08
timed| 5 min| 1 3| 0 04
A/30| 18 min| 89 4| 0 08
A/30| 3 min| 2 4| 0 01
A/30| 2 min| 9 8| 0 04
A/30| 15 min| 71| 0 1
manual| 4 min| 34 9| 0 95
A/30| 10 min| 72 6| 0 14
timed| 4 min| 5 8| 0 08
timed| 4 min| 11 3| 0 13
timed| 4 min| 10 2| 0 04
timed| 4 min| 10 6| 0 21
A/30| 4 min| 82| 0 09
A/30| 7 min| 9 74| 0 21
A/30| 3 min| 34 7| 0 03
A/30| 11 min| 87 7| 0 35
A/30| 9 min| 36 7| 0 4
A/30| 3 min| 6 2| 0 22
A/30| 5 min| 58 3| 0 26
A/30| 7 min| 52 9| 0 42
A/30| 1 min| 1 73| 0 04
manual| 5 min| 68 9| 0 66
Troubleshooting
The table below provides possible solutions for issues that may arise while using the MB45.
Problem | Possible Solutions |
---|---|
Sample burning during analysis | • Lower temperature |
• Try step or ramp program to control temperature
• Shorten runtime/exposure to heat
• Protect sample by covering with glass fiber pad
Analysis time takes too long| • Increase drying temperature
• Use rapid or step program
• Decrease sample size
• Increase surface area by using glass fiber pad
Results are not accurate| • Increase sample weight (low % MC)
• Decrease sample weight (high % MC)
• Try automatic shut-off criterion
• Review drying profile for constant weight
• Ensure homogeneous sampling
Results are not reproducible| • Ensure sample preparation is consistent and
does not influence sample
• Try automatic shut-off criterion
• Assess drying profile, sample burning or not drying sufficiently
Sample loses weight during weighing| • Allow time for instrument to cool
between measurements
• Add sample to drying pan outside of the drying unit
Sample does not reach constant weight during drying| • Use timed shut-off
criterion
• Lower drying temperature
Sample melts during heating| • Use glass fiber pad
Sample has low moisture content| • Increase sample size
Sample contains flammable material| • Follow safety directions in instruction
manual
Additional Tips for Using a Moisture Analyzer
OHAUS MB Series moisture analyzers are excellent tools for routine analysis in
the process environment The instruments are rugged, simple to operate, and
provide rapid, reliable data The devices may also be used in the research
laboratory as an investigative tool for basic scientific studies Certain
precautions should be taken to ensure that measurements made with the devices
are reproducible and as accurate as possible The following are some
suggestions for controlling operating variables for moisture analyzers:
- Allow adequate cooling between sample runs. If the machine is still very hot from the previous run, it may affect the initial weight reading of the sample and cause inaccuracy in final percentage MC
- Keep starting weight for test material consistent. Since the final reading (weight) is a factor of the drying process, consistent starting weight will minimize differences due to physical parameters of sample introduction and drying profile.
- When possible, try to control the laboratory environment. For extremely sensitive samples or for cases where sensitivity in reading is critical, consider working in an environmental chamber where temperature and humidity are tightly controlled. In general, it is best to set up the instrument in an area free of windows to minimize exposure to temperature extremes, drafts, and other environmental conditions
Case Study # 1: Sample Homogeneity
The following case study illustrates the need for sample homogeneity Here, a
sample of yellow cake was evaluated for % moisture Portions of the cake were
indiscriminately broken off the cake, then further broken apart into small
crumbs and distributed on the weighing pan The samples were dried using a step
profile (140°C 3 min , 110°C until dry) Completion of run was determined by
automatic switch-off (A30)
Results from the first three analyses:
% Moisture content = 35 03, 36 05, 32 95
Mean value = 34 68 Standard deviation = 1 58
The test results showed considerable scatter, with a very high standard
deviation. Evaluation of the drying curve and end product after drying showed
sufficient drying without sample decomposition. This suggested that the
temperature profile was appropriate for the cake and that the problem may be
due to inconsistency within the sample itself. A new sample was prepared by
taking a representative cross section of the cake, breaking it into a fine
crumb, and mixing well . A second set of analyses was conducted on the more
homogenous blend of the cake sample. The following are results from the second
set of analyses using a homogeneous cake sample:
% Moisture content = 33 60, 33 83, 33 42
Mean value = 33 62
Standard deviation = 0 2
The data obtained from these samples are shown to be more repeatable with
standard deviation within the working range of the instrument.
References
Hamburg, Morris Basic Statistics 3rd edition Harcourt Brace Jovanovich Inc ,
1985
“Electronic Spectrum” NASA Observatorium-Reference Module, 1999
“Elementary Concepts of Statistics” Electronic Textbook Statsoft, 1999
Fennema, Owen “Water and Ice” Food Chemistry 2nd Marcel Dekker, Inc , 1985
“Methods of Moisture Content Determination ” Mettler Toledo, 1998
OHAUS Europe GmbH
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education channels as well as a host of specialty markets, including the food
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Tel: 0041 22 567 53 19
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References
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