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PARTICLE SIZE
MASTERSIZER 3000
AERO SERIES
DRY DISPERSION UNITS
MAN0481
MRK1956-01
Head office:
Mastersizer, Malvern and the 'hills' logo are registered trademarks in the UK and/or other countries,
and are owned by Malvern Instruments Ltd.
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Maintenance
Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-1
Warnings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-2
Maintenance schedule . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-3
Maintenance procedures . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-4
Consumable kits. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-17
Appendix
Specification . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-1
Chemical compatibility . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-2
Regulatory Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-2
Introduction
and hardware
Introduction
This manual details the important features of the Mastersizer 3000 Aero series dry
sampling dispersion units.
The Aero S dispersion unit is designed for use with the Mastersizer 3000. It
cannot be used with the Mastersizer 3000E.
The Aero M dispersion unit is designed for use with the Mastersizer 3000E
only. It cannot be used with the Mastersizer 3000.
Warning!
The dispersion units or the samples to be measured may be hazardous if
misused. Users must read the Health and Safety information in the
Mastersizer 3000 Basic Guide before operating the system.
This manual focuses on specific issues of the Aero series dry dispersion units that
are not covered by the above manuals. Within the following chapters the manual
will detail:
Maintenance
This chapter covers all the user maintenance procedures for the dispersion units.
This includes a maintenance schedule and associated maintenance procedures for
inspecting and cleaning each dispersion unit and its respective components. Spe-
cific procedures for inspecting and cleaning the flowcell windows are described.
Appendices
This chapter details the useful specifications of each dispersion unit and identifies
the chemical compatibility of the dispersion unit components that may come into
contact with the sample. Additionally it provides the important regulatory informa-
tion to which the dispersion units are compliant.
4 5 2 3 1
ill 8867
Note
For clarity the Aero images in this manual are shown with the (right-
angled) high energy disperser fitted. When the (straight) standard disperser
is fitted the Aero unit will be positioned facing to the right along the bench.
1 2
ill 8868
The air supply and vacuum extraction system is then connected and the sample tray
vibrated.
With the sample feed tray vibrating the sample exits the hopper and travels down
the tray until it eventually falls into the main feed mechanism - the venturi dis-
perser.
The rate at which the sample is fed into the venturi disperser is governed by the
amplitude of vibration on the feed tray, (controlled from the software) and also by
the gap set between the feed tray and hopper (Aero S) or tray gate (Aero M) on the
sample tray.
As the sample falls through into the funnel of the venturi disperser, it is accelerated
by compressed air within the centre of the venturi disperser where agglomerates are
dispersed. The sample is then directed through the dry cell fitted to the Master-
sizer optical unit, where it is measured and then collected by the vacuum extracting
system at the rear of the dry cell.
9 9 6 7 8
ill 8869
Warning!
Do not run the dispersion unit without the air filter fitted, otherwise
acceptable sound emissions will be surpassed.
The fitting on the lid allows clean filtered air to be drawn into the sample area.
Using the dispersion unit without the filter will affect the measurement perfor-
mance and create excessive noise levels.
Sampling area
The sampling area is where the sample is added into the dispersion unit prior to
being measured. There are five primary parts to the sample area; these are described
below in the order the sample would progress through the sampling area.
D
A
ill 8783
The Aero M is the same but uses a different flow control / tray arrangement.
There is no sample hopper on the Aero M.
Note
If a tray is used that requires a hopper, then the hopper must be fitted, or
the unit will not work and will stay in standby mode until the hopper is
inserted.
The hopper attached to the sample tray is used as a method of controlling the flow
rate of the sample into the tray and subsequently also into the venturi disperser.
This is done by rotating the top of the hopper, therefore varying the aperture gap
between them. The hopper has markings positioned around the hopper to indicate
the setting of the aperture gap.
To attach the hopper to the sample tray:
1. Slide the hopper lock lever towards the front of the unit.
2. Insert the hopper assembly into the location holes on the sample tray - it can
only be inserted one way.
3. Secure the hopper by sliding the lever fully back.
ill 8780
Removal is the reverse of the procedure.
Mesh baskets and ball bearing (Aero S only)
Prior to the measurement, sample can be placed into one of the supplied mesh
baskets (1mm or 2mm), which in turn is pushed onto the top of the sample
hopper.
The mesh baskets, and the added ball bearing, help smooth the flow of sample
as they effectively store the sample within the assembly for a short period.
Additionally the ball bearing helps break up any loose agglomerates within the
sample before it falls into the hopper.
It is not necessary for the mesh basket or ball bearing to be used; the sample can
be placed directly into the sample hopper if desired. This will depend upon the
characteristics of the sample to be measured.
Sample tray (Aero S)
The sample tray receives the sample to be measured from the hopper assembly; the
sample feeds down the sample tray as it is vibrated. The tray is channelled so that
the sample is deposited into the centre of the funnel of the Venturi disperser.
The rate at which the sample is fed into the venturi disperser is governed by the
amplitude of vibration of the sample tray, this is controlled from the software.
Three sample trays are available:
Standard tray The standard sample hopper and tray pair provided with
(General purpose) the Aero dispersion units is the General purpose hopper/
tray pair. This is most suitable for free-flowing materials
and materials having broad size distributions (between 1 to
3500 microns where larger samples need to be measured
to obtain statistical significance.
Micro tray The micro tray is designed for samples where either very
little material is available for sampling, or the material is
prohibitive expensive for repeated measurements.
No hopper is included with the micro tray; the sample is
placed directly onto the tray
Macro tray The macro tray is designed to hold more sample than the
micro tray insert, but much less than the standard tray. It is
intended for use for larger samples where the small size of
the micro tray may prove a problem in terms of reliable
measurements, but where it is critical that as little sample
as possible is used. The macro tray is a good compromise
between the standard and micro options.
No hopper is included with the macro tray; the sample is
placed directly onto the tray
A tray gate assembly at the end of the sample tray additionally controls the flow.
This is done by altering the height of the gate above the sample tray.
To adjust, loosen the knurled thumb screws on either side of the gate, move
the gate up or down to the desired position, then secure the thumbscrews.
ill 8894
ill 8781
Removal is the reverse of the procedure.
Note
If the sample hopper/tray is not attached and locked onto the vibration
plate correctly, then the unit will not work and will stay in standby mode
until the hopper is inserted.
The ceramic option dispersers are designed for abrasive materials such as cement.
They can be identified by a couple of matching rings on the venturi body and
receiver tube, as shown below.
The stainless steel variant has no rings present.
ill 8827
Connection of the sampling tubes to the air cell is simply push on and twist to
secure the connection lock.
Over time different venturi dispersers may be developed that can be used for sam-
pling different grades and sizes of sample and other applications. Encoding in the
venturi disperser will automatically identify the dispersers when they are attached
to the dispersion unit, with the disperser type being reported in the sample meas-
urement and records.
Warning!
Take care when removing the venturi not to trap fingers between the tray
holder (vibration plate) and the venturi.
Note
The Aero S disperser will only fit on the Aero S.
The Aero M disperser will only fit on the Aero M.
For more information of cleaning the venturi disperser refer to the Maintenance
chapter.
ill 8782
Status indicator
A status indicator illuminates to indicate the operating condition when the disper-
sion unit is powered up:
Blue - full intensity
The dispersion unit is functioning correctly and the cell has been loaded into
the optical bench. (i.e. the dispersion unit is “active”).
Blue - pulsing
The dispersion unit is functioning correctly but its cell has not been loaded
into the optical bench. (i.e. the dispersion unit is at “standby”)
If communication has failed with the optical unit the status indicator will also
be on standby, but the optical unit indicator will be off.
Air in connector
The compressed air line is connected here. The compressed air is used to disperse
the sample. The input range is from 5.5 to 8 bar g, but should nominally be set to 6
bar g.
Refer to the Mastersizer 3000 User Manual and Basic Guide for the site
requirement details of the compressed air supply.
The outlet from the compressor must be fitted with a push-fit adapter capable of
taking a 6mm o/d polyurethane pneumatic tube.
Warning!
The air pressure regulator fitted to the Aero has a maximum input pressure
limit of 10 Bar. If there is a possibility that the air supply could exceed this,
then a protection device ensuring this limit is not exceeded must be fitted.
Caution!
The air line supply must be dry, free from oil and filtered to less than
0.01mm. Failure to meet this specification will permanently damage the
dispersion unit and invalidate the warranty.
CAN connection
The CAN connection provides both the communications and power to operate the
dispersion unit.
The CAN cable is connected from the CAN connection to one of the CAN con-
nections on the side of the optical unit.
Auxiliary connector
The Auxiliary connector (AUX) is used to connect to the Ancillary switching unit,
described below, and any additional accessories that can be used with the dispersion
unit.
Feet
The feet are used to level the dispersion unit horizontally so that an accurate feed of
the sample is delivered into the venturi disperser. The sample should feed centrally
along the sample tray and not move to the side.
To level the dispersion unit
The sample tray must be level in both horizontal axes. Rotate the two feet at the
back of the unit to level the unit on the bench as required.
1. Remove the sample hopper from the sample tray.
2. In one axis, place a spirit level on to the sample tray and adjust the feet until
level.
3. Place the spirit level in the other axis, and again adjust the feet until level.
4. Repeat both adjustments until sample tray is level in both axes.
Lifting holds
Recesses on either side of the dispersion unit body can be used for lifting and trans-
porting the unit.
Additional components
Ancillary switching unit
The Ancillary switching unit is an external control accessory that is used to switch
on the vacuum unit required for the sample extraction during each measurement.
Power into the switching unit
Connect mains supply to this port. Input supply: 100-240V / 50-60Hz.
Power to the vacuum unit
Connect the vacuum unit to this port.
Reset button.
The unit uses an internal resettable fuse, press this button if the unit requires reset-
ting.
1 3 4 2
ill 8656
Control.
Connects to the dispersion unit AUX connection. Communication to the switch-
ing unit is done via the dispersion unit. The software will request the dispersion
unit to switch on the vacuum unit when required.
Note
The on/off switch of the vacuum unit must be set to On to allow the ancil-
lary switching unit to work.
Note
An adaptor cable is required to connect an IEC 60320 C13 power cable (as
used by the Nilfisk GM80 vacuum cleaner) to the higher-rated IEC 60320
C20 connector on the ancillary switching unit. Contact Malvern Instru-
ments for more information.
Each Aero dispersion unit will be connected to a matching Aero series dry cell.
The dispersion unit continually delivers the sample from the dispersion unit to the
Aero dry cell and through the analyser beam of the optical unit so that a measure-
ment can be performed.
The cell windows in the dry cell are critical parts of the measurement optical path
of the system and should be kept clean and free from scratches at all times. Refer to
the Maintenance chapter for details on cleaning/maintaining the cell.
1
6
2
7
3
ill 8779
Cell shroud
The cell shroud prevents stray light entering the measurement area that may affect
a measurement. More importantly, the cell shroud stops human access to laser
radiation. The cell shroud on the dry cell also reduces noise emissions
The cell shroud incorporates an arm that will open a mechanical shutter when
inserted into the optical unit. With the shutter open laser light is allowed into the
sample area. When the cell is withdrawn the shutter will move back into position to
prevent the emission of any laser light.
The system should never be used if the cell shroud or shutter arm is damaged.
Warning!
Never attempt to lift the optical unit by the locking handle of the cell. Read
the Health and Safety section in the Mastersizer 3000 Basic Guide for
details of correct moving techniques.
When the cell is inserted into the sample area of the optical unit, a locking motor
will pull the cell down and lock it into a defined measurement position. This
ensures that the cell is always optimally located before any measurements are per-
formed.
To remove the cell, press the button on the cell handle. This will release the lock-
ing motor and raise the cell slightly ready to be withdrawn from the optical unit.
Sample inlet
The sampling tube from the dispersion unit is connected to this inlet.
Connecting the sampling tube.
To connect the sampling tube:
1. On the sampling tube, line up the catches on the collar to the pins on the dry
cell connection.
2. Holding the collar, push the sampling tube onto the connection, then rotate
the collar to lock the tube on.
Removal is the reverse of the procedure.
Vacuum port
This connects up to the vacuum connection on the rear of the optical unit. A vac-
uum unit must be used to prevent samples being discharged into the laboratory.
ill 8778
Inspect the seal at the rear of the dry cell before each use. If the seal is damaged the
operation of the dry cell and measurement will be reduced.
To connect the vacuum hose, an extraction elbow needs to be fitted to the back of
the unit; this will replace the blanking plate normally used when any Hydro wet
cell is fitted. The elbow can be positioned in any position suitable for the vacuum
unit connection.
Note
The on/off switch of the vacuum unit must be set to On to allow the
Ancillary switching unit to work.
The air intake filters must be fitted at all times; though providing the vacuum unit
and hose are attached, the blanking plate does not require fitting when measure-
ments with the Hydro dispersions units and wet cell are performed.
If the vacuum unit and hose are not available the blanking plate must be fitted.
Note
The vacuum hose, used to connect to the vacuum port, requires an inter-
nal diameter (i.d.) of 38mm
AERO
10
3
2
1
8
ill 8659
The Mastersizer 3000 User Manual details specific connections to the optical
unit.
Depending on the vacuum cleaner attached, an additional power cable may
be required. Refer to the Mastersizer 3000 Basic Guide.
Making a measurement
Making a measurement using the Aero dispersion units is fully documented in the
Mastersizer 3000 User Manual. Refer to that manual for details.
The dispersion units can be controlled in several ways;
Manually or automatically by running an SOP. The system automatically
detects which dispersion unit and cell is connected. If more than one disper-
sion unit is connected, the system detects all dispersion units connected, but
only the dispersion unit that has its cell installed on the optical bench will be
“active”.
Alternatively the dispersion unit can be controlled by a separate manual acces-
sory control window. This enables simple control of the dispersion unit, allow-
ing individual selection and operation of the unit’s functionality.
These are described in the following pages.
Note
The software will automatically recognise which disperser is in use (stand-
ard or high energy) and the material type used to make the venturi (stain-
less steel or ceramic).
2. Select an SOP template from the list in the New SOP window or click the
From existing SOP... button to locate an SOP in the file system that fulfils
(or is close to) your required criteria.
3. The SOP Editor window is now displayed. This will be configured to apply to
the dispersion unit selected.
4. Complete the SOP Editor as described in the Mastersizer 3000 user manual.
Section Description
Air pressure Use this slider bar to set the air pressure at which the sample
is circulated (from 0-4 bar, in 0.1 bar increments). Lower air
pressures tend to be better for fragile particles, higher air
pressures for agglomerates or metallic particle samples
Feed rate Use the slider bar to set the rate at which the sample is fed
into the system - effectively this controls the vibration speed
of the feed tray. The correct feed rate is one at which the
sample is vibrated evenly along the feed tray and gives the
required obscuration - this rate is best established as part of
a method development process.
Configuration Use the pull down menus to select both the Venturi and Tray
types to be used in the measurement.
Input the hopper gap that has been manually set for the
sample measurement.
The Cleaning options allow you to specify a clean sequence for the dispersion
unit. This ensures that all traces of the sample just measured are removed so that no
contamination of the next sample occurs. Cleaning following a measurement is
essential to ensure that background noise, consisting of particles agglomerating
within the system and forming accumulations, is minimized.
Section/option Description
Clean Sequence Each Clean type specifies a set number of cycles (nothing
further is changed in the cleaning method). Select a Clean
type of either Quick, Normal, Extensive or Custom. If Cus-
tom is selected the user must also manually specify the
number of Clean cycles.
If measuring the same sample type in succession a Quick
clean may be sufficient.
If making the last measurement of the session, it is prudent
to perform an Extensive clean to ensure that the system is as
free as possible from contamination in readiness for the next
measurement session.
Air pressure Use the slider bar to set the air pressure at which any
remaining sample is removed (from 0-4 bar, in 0.1 bar incre-
ments).
Feed rate Use the slider bar to set the rate at which the remaining sam-
ple is removed - effectively this controls the vibration speed
of the feed tray.
Tip
The same controls are also available from the Active accessory control
feature (choose Tools-Accessories from the control ribbon).
The accessory controls panel for the Aero S is shown as follows (in this example the
Air pressure/Feed rate have been set):
Section/option Description
Disperser / Tray Displays the configuration of the dispersion unit.
(Aero S only) I.e. Standard venturi disperser and General purpose trays
are fitted
Standby / Air Standby - By default the Aero is in standby mode when the
flow / Feed but- accessory is connected and powered up, but not active. In
tons this mode the front LED is pulsating.
Flow - Activate the air flow.
Feed - Starts the vibrating feed tray. Selecting this option
also automatically turns on the Air Flow.
Air pressure Use this slider bar to set the air pressure at which the sample
is circulated (from 0-4 bar, in 0.1 bar increments). Lower air
pressures tend to be better for fine or fragile particles, higher
air pressures for agglomerates or metallic particle samples.
Feed rate Use the slider bar to set the rate at which the sample is fed
into the system - effectively this controls the vibration speed
of the feed tray. The correct feed rate is one at which the
sample is vibrated evenly along the feed tray and gives the
required obscuration - this rate is best established as part of
a method development process.
Clean Select the cleaning sequence required: Quick (1 cleaning
(Aero S only) cycle), Normal (3 cycles), Extensive (5 cycles). The disper-
sion unit will perform a clean sequence, for the selected
duration, that will remove any remaining sample from tray
and the disperser.
Section/option Description
Clean Select the cleaning sequence required: Quick (1 cleaning
(continued) cycle), Normal (3 cycles), Extensive (5 cycles). The disper-
(Aero S only) sion unit will perform a clean sequence, for the selected
duration, that will remove any remaining sample from tray
and the disperser.
A Custom vacuum sequence can be configured. Clean
duration, air pressure and feed rate set as appropriate for the
sample and application.
ton .
Note: In the Active accessory control window (Tools-
Accessories) pressing Clean will start the cleaning
sequence
To help cleaning the unit - when the unit is in standby and
with the air supply turned off - the Vacuum can be manually
turned on independently of the air and feed. The
lid can then be opened and any remaining sample brushed
into the vacuum for extraction from the system.
Abort Stops all operations and close all valves. The accessory is
returned to the Standby status.
Maintenance
Introduction
This chapter covers all the user maintenance procedures for the dispersion unit. Do
not attempt any maintenance procedure not specified here. This chapter covers:
Maintenance schedule
This section suggests a maintenance schedule for inspecting and cleaning the dis-
persion unit and its respective components.
Maintenance procedures
This section describes how to perform various maintenance procedures and actions
identified in the schedule to help ensure the dispersion unit is kept working opti-
mally. Maintenance procedures described are:
Cell window inspection and cleaning procedures
This section includes topics on:
How to inspect the cell windows, in case of poor background results.
Cell windows removal and inspection.
How to inspect the quality and cleanliness of the windows.
Appropriate cleaning techniques.
Dispersion unit cleaning
This section describes how to clean the various components of the dispersion unit
that have been identified in the maintenance schedule. This section includes topics
on:
Cleaning of covers.
Sample tray cleaning.
Cleaning after a measurement.
Checking and replacing of sample tubing, vacuum cleaner bags and air vac-
uum.
Warnings
General
Warning!
The dispersion unit contains no internal serviceable parts. Never attempt
to remove the covers of the optical bench or dispersion unit. Removal of
the covers invalidates the warranty and may expose the user to dangerous
laser radiation.
Warning!
Failure to follow these guidelines could result in the emission of laser radi-
ation or exposure to hazardous voltages. Laser radiation can be harmful to
the body and can cause permanent eye damage.
Aero dispersion units do not contain a laser but are connected to the optical
bench that does.
Warning!
Before carrying out any maintenance operation, read and observe the safety
warnings listed in the Mastersizer 3000 Basic Guide.
Warning!
Before cleaning, always disconnect the unit from the power supply and
computer and disconnect all electrical cables.
Maintenance schedule
Follow the maintenance schedule below to keep the dispersion unit working well.
This list is only a guide; the exact frequency at which to perform tasks depends on
many factors, including:
The samples being measured.
The environmental conditions.
The number of measurements made (frequency of use).
The procedures indicated below are described in the following pages of this chap-
ter.
Procedure Period/situation
Inspect cell windows The cell windows should be checked for general
for dirt and scratches cleanliness every day, or if during a background
measurement either of these is seen:
One of the first few detectors displays a value
above 100 light energy units.
Background signal over 20 light energy units
recorded by one of the detectors above detector
20.
Either of these situations would indicate a poor
background; this will effect the quality of any meas-
urements.
Clean the unit Check/clean sampling area (sample tray and hopper
assembly, venturi disperser) at least daily
Check/clean air intake filters monthly
Check/clean vacuum cleaner bag weekly
Check/clean compressed air supply filters monthly
Clean the covers Once a month.
Replace the venturi At least quarterly dependent upon sample type used.
disperser tubing
Perform a Quality Audit At least once a week or as internal quality procedures
Standard measurement specify.
Maintenance procedures
Inspection of cell windows - Poor background
The cell windows should be inspected for cleanliness every day and after each
measurement session. Problems which indicate the need for cleaning or mainte-
nance are the following. These expand on the situations in the first row of the
maintenance schedule table.
ill 8830
If your system displays high detector channels, refer to the Cleaning the cell
windows section as described later in this chapter and remove and clean the
cell windows.
Note
The cell window faces must not be touched directly during the removal
and replacement procedure. Lens tissues should be placed over the win-
dow faces where necessary.
ill 8784
Caution!
Do not wipe the windows with an ordinary dry cloth as this will cause
scratches. Always use the procedure below to clean the surfaces.
Note
The cell windows are part of the optical system and removing them for
cleaning will change their position. Remember to add an Align stage to the
next measurement sequence or click the Align button.
ill 8661
Repeat the procedure for removing the remaining cell window and seal from the
other side of the cell.
Caution!
The outer faces of the cell window are optically coated; treat them with the
same care as a camera lens.
ill 8662
Without touching the window faces (use a lens tissue to hold), remove a cell
window from its protective paper wrapping.
Hold by the ground edges of window. Ensure that the face with the larger diameter
must be facing down (outwards) when inserted into the dry cell cover plate.
Once inserted, move the window so it is central in the plate.
ill 8663
Take a dry cell seal and carefully place it on the gap around the outside of the cell
window and cover plate.
ill 8664
Using a clean lens tissue carefully push the seal into the gap. Continue until the
seal is securely inserted. The seal must be of equal height all way round the win-
dow, with no bulges in the seal.
ill 8665
General guidelines
Laser light scattering systems rely on the cleanliness of the optical components (e.g.
cell windows). Dust on the optics causes light scattering; the system will respond to
particles on the optics in a similar way to particles presented in the flow cell. The
signal from dirty optics will contribute to the background signal, so it is good prac-
tice to keep the optical components as clean as possible.
When optical components have been used for a long period, even in the cleanest
laboratories, assume that they have traces of fine grit on them as well as the obvious
dust. Fingerprints usually contain grease and grit so need careful cleaning.
Caution!
If any silicone oils are deposited on the glass surface they adhere so
strongly that it is impossible to clean them off, ruining the component.
Cleaning steps
Depending upon the quality and cleanliness of the windows, use the appropriate
cleaning technique as described. Read through the below steps to determine the
correct techniques required; these are described in order of severity and contami-
nation.
It is recommended to inspect the cell window in reflected light from a fluorescent
tube or other light source.
Gritty surface particles / Smeared surface - with grit
If the surface has fingerprints on it or has not been cleaned for a long time, assume
there is grit present. First wash the surface then wipe it as described; refer to the
Washing cell windows and Wiping cell windows sections below.
Dusty surface:
If the surface is just dusty use a clean air aerosol duster or soft brush; refer to the
“Clean air” aerosol dusters and Brushing optical surfaces sections below. If
marks are present afterwards wipe the surface as described in Wiping cell win-
dows.
Smeared surface - no grit
If the surface is smeared and you are sure there is no grit on it, wipe the surface as
described below in Wiping cell windows.
Caution!
The outer faces of the windows have an anti-reflective coating and are
more prone to scratching than the inner surfaces. Be careful not to touch
the faces of the windows or put them down on dirty surfaces.
boil away leaving a drying mark on the surface. This effect can be limited by keep-
ing the aerosol perfectly upright, and testing the aerosol first by squirting it in a safe
direction to ensure that the nozzle is clean.
Once the dust is removed, wipe the cell windows as described in Wiping cell win-
dows below to produce the final clean surface.
3. Use each tissue for one pass only. This is the only way to ensure a clean
undamaged surface. If a wipe has done its job it will be loaded with grease from
the surface. Wiping the surface again will just deposit the grease back on the
surface. Worse, if the wipe has lifted off some remaining grit this could scratch
the clean surface.
4. Marks from the o-rings usually form an oily line around the outer part of the
optical surface. With surfaces contaminated in this way, wiping from the centre
outwards prevents the oily mark from being spread from an unimportant area
across the window centre. If there are smears associated with starting the pass
in the centre of the surface, once the o-ring marks have been completely
removed give the surface a single wipe from side to side.
5. Re-inspect the window; if it’s still marked, repeat the procedure with a new
clean tissue.
Note
If marks remain, use a liquid cleaner such as Ethanol or Propan-2-ol. This
can be soaked on a cotton wool bud and wiped across the window gently.
After one pass over the window discard the bud to avoid scratching. Re-
inspect the window and repeat until clean.
Caution!
The surfaces of the system may be permanently damaged if samples or dis-
persants are spilt on them. If a spillage occurs, disconnect the system from
the power supply before carefully cleaning it up.
Warning!
If the dispersion unit has been used to measure hazardous materials (see
the notes in the Health and Safety information), the vacuum used must
have an efficient filter that stops particles being ejected into the atmos-
phere.
Warning!
Refer to the Material Safety Data Sheets supplied with the material
before beginning any cleaning routine.
We recommend cleaning the dispersion unit periodically using the vacuum nozzle
a soft brush.
Disconnect the dispersion unit from the CAN connection before proceeding with
any cleaning.
2 1
ill 8810
Note
Ensure the venturi disperser is fully dry inside and out before reusing. It is
recommended to flush the dispenser with ethanol or isopropanol after first
cleaning with water.
Every 20 measurements:
Inspect and, if necessary, clean the cone area under and around the mesh.
Inspect the contents of the mesh basket to see if large sample agglomerates are
gathering. If so, remove the ball bearing (if used) and clean the mesh basket.
Brush the tray/hopper and surrounding area clear of sample, taking care not to
introduce dust onto any optical components.
Sampling tube
The bore of the sample tube will eventually become coated with a layer of powder.
This can be removed by running a cleaning sample such as glass beads through the
feeder on a regular basis. Once this fails to clean the tubing, replace it.
Note
It is recommended that any vacuum unit used with the dispersion unit is
equipped with HEPA filters, or can have HEPA filters fitted.
Consumable kits
Consumable kits and additional spares for maintaining the Aero series dry sampling
dispersion units are available from your Malvern representative. Please contact
them for full details and requirements.
The consumable kit include the following components:
Aero consumable kit
Appendix
Specification
The following table details the specification of the Aero dispersion unit and Aero
series dry cell. Full specifications of the optical unit and the Mastersizer as a com-
plete system can be found in the Mastersizer 3000 User Manual and Basic
Guide.
All specifications correct at time of publication, but may be subject to alteration.
Size range
-- Aero S 0.1 to 3500 μm*
-- Aero M 0.1 to 1000 μm*†
* Sample dependent.
† When used with the Mastersizer 3000E
Chemical compatibility
Components of the Dispersion unit that may come into contact with the sample
are manufactured from materials that are considered to give the widest protection
from chemical attack. However, it is important to check that any sample or titrant
used is chemically compatible with the materials mentioned. The table below indi-
cates the components that may come into contact with either sample or dispersant.
Warning!
It is advisable that the chemical compatibility is checked against the materi-
als identified below before inserting a sample. It is also recommended that
a test is performed on the material with the sample before more permanent
usage is undertaken.
Any cleaning and maintenance procedures necessary are described in the Mainte-
nance chapter of this manual.
Component Materials
Sample tray assembly Stainless steel 316
Venturi disperser
- Stainless steel Stainless steel 303/410 hardened
- Ceramic Stainless steel 303/410 hardened/High purity alumina
Mesh basket Stainless steel 316
Ball bearings Stainless steel 316
Sample pipes to cell Carbon impregnated polyurethane
Cell Borosilicate Glass / Stainless steel 316
Vacuum extraction elbow Carbon filled acetal
Note
For chemical compatibility of the Mastersizer 3000 optical unit, refer to
the Mastersizer 3000 basic guide.
Regulatory Information
Regulatory information for all Mastersizer 3000 instruments and dispersion units,
can be found in the Mastersizer 3000 basic guide.
www.malvern.com
PARTICLE SIZE
MASTERSIZER 3000
AERO SERIES
DRY DISPERSION UNITS
MAN0481
MRK1956-01