Porosity or Permeability
Porosity or Permeability
Porosity or Permeability
porosity or permeability
It is the property of sand which permits the steam and other gases to pass through the sand
mould.
depends upon
grain size, grain shape, moisture and clay components of the moulding sand.
Transverse test
The shatter index
• shatter test is used as an indicator of sand toughness
• The ability to deform rather than fracture under shock loading.
• The standard compression test cylinder is ejected from its mould and allowed
to fall from a fixed height of 1.83m on to a flat steel anvil.
• Fragments retained on a concentric 13.2mm aperture BS410 sieve are weighed,
together with the residual core from the anvil,
• the shatter index is this weight expressed as a percentage of the total weight of
the specimen
• A low value is an indication of poor lift, or friability in pattern withdrawal and
subsequent handling, whilst too high a value is associated with unsatisfactory
moulding qualities resulting from excessive clay or water content.
• Values of 50–85 represent the mouldable range.
Surface hardness
• The hardness of a compacted sand surface can be determined using portable
spring loaded indentation testers
• For the measurement of green hardness, a spherical or conical indenter is used
depending on the expected hardness level
• the depth of penetration from the flat reference surface of the instrument
corresponds to an empirical scale of hardness in the overall range 0–100.
• The hardness can be measured on actual mould surfaces to check the degrees
of uniformity and the ramming efficiency.
Deformation
• The deformation behaviour of moulding sands has received less consideration
than the properties reflected in the above tests.
• Deformation can be determined during the green compression test by
measurement of the decrease in length of the cylindrical specimen to the point
of failure, whilst more comprehensive data can be derived from full stress–
strain curves,
Permeability
• Permeability is determined by measuring the rate of flow of air through a
compacted specimen under standard conditions.
• The test for green permeability is carried out on the A.F.S. standard
cylindrical specimen, retained in its ramming tube
• The permeability meter, incorporates a graduated bell of 2 litres capacity
containing a volume of air over water.
• A tube from the air enclosure communicates directly with the specimen
tube, placed over an ‘O’-ring seal, so that the air can escape through the
specimen as the bell descend.
• The time for exhaustion of 2 litres of air is determined.
• The permeability number P is defined as the volume of air in cm3/min
passing through a specimen of length 1 cm and cross-sectional area 1 cm2,
under a pressure difference of 1 cm water gauge:
P = Vh/atp
where V = volume of air, cm3
h = height of specimen, cm
a = c.s.a. of specimen, cm2
t = time, min
p = pressure difference, cm water.
Using the standard apparatus and technique,
the permeability may be derived directly from the formula
P = 3007.2/t
where the time t is expressed in seconds.
• A standard orifice, of small cross section in comparison with the porosity of
the specimen, is placed between the pressure chamber and the specimen.
• The pressure between orifice and specimen now lies at a value
intermediate between the chamber pressure and atmospheric pressure,
depending on the permeability of the specimen.
• The value is derived directly from this pressure, measured by calibrated
water manometer.
• A similar principle is embodied in the portable quick reading instrument
• The required air pressure is in this case generated by a high speed electric
fan and the pressure drop is indicated on a sensitive gauge calibrated
directly to read the permeability number.
• Either type of permeability meter can be used in conjunction with a flexible
tube and contact pad to provide a direct indication of the level of
permeability at any flat mould surface.
• Permeability determinations on dried or hardened sands require a modified
specimen holder enabling the cylindrical walls of the test piece to be sealed
against the bore surface of an enlarged tube, using molten wax or an
inflatable rubber sleeve
Bench life
• Compression tests are made on specimens rammed at successive intervals of five
minutes from mixing.
• The bench life is defined as the time to reach the value of 10 kN/m2, beyond which the
strength of subsequently compacted material will be prejudiced by interruption of the
bonding process already under way in the loose sand.
• Other relevant time intervals can be applied, depending on the sensitivity of the
mixture under test.
Strip time
• Numbers of compression test specimens are moulded in multi-gang boxes immediately
after mixing.
• Tested at intervals to detect the time at which the strength reaches350 kN/m2.
• A full strength–time plot of the type shown, can be developed from this form of test to
characterize the setting behaviour in full, including the maximum potential strength of
the material.
Scratch hardness
• A four point spring loaded penetrator is contained within a concentric
reference surface which is pressed against the hardened sand surface.
• The penetrator is manually rotated though a fixed number of revolutions,
normally two, and the depth of penetration is shown on a dial gauge as an
indication of relative surface density and scratch resistance.
Impact penetration
• A sharp spring actuated probe graduated in 1 cm divisions, is repeatedly
triggered by manual pressure against the sand surface,
• And the number of blows required to reach a given depth represents the
relative resistance of the sand body to penetration.
• The test can be carried out on production moulds or on sample 10 cm
cubes, molded and tested whilst in the corebox.
• A valuable feature of this test is its ability to explore the rate and depth of
hardening and to detect any lack of through cure
• plots of numbers of impacts against penetration depth enable the degree of
uniformity to be investigated.
Gas evolution
• The rate and volume of gas evolved from a dried sample of hardened sand
can be determined using a sealed, temperature controlled, silica tube
furnace with provision for a nitrogen atmosphere.
• The weighed sample is propelled into the hot zone of the inert gas-filled
tube, normally at a temperature of 850°C, and the pressure rise is
continuously recorded until a maximum is attained.
• The pressure readings can be converted to volumes, using a calibration
chart derived from the known total evolution from a standard substance.
• Both rate and total volume are significant in relation to potential gas defects
in castings.
Impact penetration tester with internal spring
loaded hammer
Hot distortion
• The hot distortion test is carried out on a flat strip sand specimen which is fixed
at one end and loaded in cantilever mode at the other
• The underside is heated and the deflection at the loaded end continuously
measured.
• Upward movement due to initial expansion of the lower layers of the strip is
followed by sagging with the progressive thermal softening and eventual
breakdown and collapse of the material.
• Strain–time curves provide a guide to the behaviour of different binders and
curing conditions.
• Typical curves representative of hot box, cold set and silicate bonded sands,
including the influence of iron oxide additives, were produced in a
comprehensive study by Morgan and Fasham
Schematic arrangement of hot distortion test
High temperature properties
• High temperature tests are particularly relevant to the study of mould and core
materials, since they simulate in some degree conditions met in the casting
process.
• more suited to longer term laboratory assessments than to routine testing
• Gas evolution and hot distortion tests - given their particular value in relation to
the chemically hardened sands.
• hot strength test include the determination of compressive strength to failure at
specified temperatures, -prior soaking periods for the specimen to reach the test
temperature
• measurements of total deformation can also be obtained from the same test
• To assess the retained strength, a property relevant to knockout behaviour, the
specimen is put though the thermal cycle, but cooled to room temperature before
testing to failure
• Collapsibility can be assessed through determination of the time to failure under
constant load
• more suitable than isothermal hot strength tests for organically bonded sands, in
which the bond can be completely decomposed during the soaking period.
• Free expansion in the absence of loading can also be measured using a dilato meter
• this type of measurement can be relevant to certain types of sand defect incastings
High temperature and retained strengths of sodium silicate bonded sand
Moisture testing
• Moisture content is readily determined by loss in weight on drying at 110°C.
• Various rapid aids are employed, including balances directly calibrated to
read the moisture content of a standard sample after drying;
• samples can be dried by the passage of hot air through a filter cloth tray.
• For shop control the Speedy moisture tester can be employed.
• This makes use of the reaction
CaC2 + 2H2O = Ca(OH)2 + C2H2
• The sample is placed in the cap of a metal flask fitted with a pressure gauge
and an excess of the carbide reagent placed in the flask body.
• The flask is closed, clamped and shaken and the acetylene pressure
provides a direct reading of moisture content on the gauge.
• Electrode probe devices have been used to determine the moisture content
of loosely heap sand, but are not employed for the accurate assessment of
samples.
• an electrical method employing measurements of microwave absorption in
compacted samples is employed with success to control moisture in
mechanized system sands
Active clay
• The live bentonite clay present in a sample of reconditioned sand
can be determined by the methylene blue test,
• discriminate between active clay and other particles of similar size
which are included in the normal clay grade determination.
• Methylene blue dye, when added to an acidified slurry of clay and
water, is adsorbed by the clay to a point at which the appearance
of excess dye can be observed by spotting drops of the liquid on to
a filter paper.
• weighed sand sample is agitated and heated in the selected initial
solution, using stirring or ultrasonic means.
• The standard methylene blue solution is then progressively added
from a burette until the spot tests reveal the end point, which is
represented by a halo around the spot.
• The volume of the standard solution required can be directly
related to the active clay content using an appropriate calibration
curve.
pH and acid demand
• The pH value of a solution, a reciprocal function of the hydrogen ion
concentration, is the standard representation of the degree of acidity or
alkalinity on a scale from 1 to 14.
• Values from 1–7 represent acid
• 8–14 alkaline condition
• The pH value can influence the behaviour of clay binders
• readily measured using a meter depending on electrochemical potentials.
• In chemically bonded sands employing acid catalysts, account needs to be
taken of the presence of alkalis already present in the base sand before the
addition of the binder.
• Since pH measurements are only influenced by substances in solution, the
purpose of the acid demand test is to assess the full effect of insoluble alkalis
as well.
• The test involves the introduction of a standard volume of hydrochloric acid of
known concentration to a sample of the sand suspended in water.
• The acid reacts with the whole of the alkali content, leaving an excess of HCl.
• This can be quantified by titration with a standard solution of sodium
hydroxide, so enabling the true acid demand value of the original sample to be
determined by difference.
Loss on ignition
• Loss on ignition is employed to determine the presence of organic
and other gas forming materials present in the sand mixture or its
individual constituents, including new and reclaimed sands.
• A weighed sample of pre dried material is fired in a silica crucible
held in a muffle furnace at 925°C for 2 hours.
• The percentage loss in weight is determined and arises from the
volatilization, oxidation and decomposition of substances forming
gaseous products.
• These include additions or residues of carbonaceous additives
such as coal dust, chemical binders, cereals, and carbonates in sea
sands.
• Although the test does not discriminate between such sources, it
does in practice provide a check on the consistency of binder
contents and the condition of new and reclaimed sands.
• Actual volatiles can if necessary be separately determined by
similar tests conducted in inert atmospheres.