(2)viscosity measurement -2015

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    VISCOSITYMEASUREMENT OF

    GLASS

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    1 Pa-s = 10 P

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    1 Pa-s = 10 P

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    EXPERIMENTAL ISSUES

    1. elevated temperatures

    the materials used in the construction of the apparatus must becapable of withstanding the required temperatures withoutundue deformation under the mechanical or thermal stressesinvolved, and without being corroded signicantly by the

    atmosphere or by the melt.

    our choice!platinum-rhodium alloys, or else pure ceramics such asrecrystalli"ed alumina.

    2. glass melts is highly sensitive to temperature

    # provide a furnace chamber with the minimum possibletemperaturevariation throughout the volume occupied by the sample# $onstancy to within 1%$ should be the aim.

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    3. the measurement of temperature

    a. thermocouples so placed as to give the best estimate of the

    samples average temperature.

    b. Thermocouple wires should enter the furnace cavity long a route

    designed to minimize differential thermal gradients and electrical noise

    pickup

    c. the wires should be sufficiently long to allow proper connection to the

    measuring device.

    d. thermocouples suffer aging in service to some extent, it isnecessary to calibrate them at intervals against a subsidiary standard

    thermocouple reserved for that purpose.

    4. Sample preparation and handling

    i. avoid clearly visible inhomogeneities or contamination

    ii. Excessive heating can cause change of composition due to

    volatilization or reaction with the surrounding atmosphere

    iii. &rinding a sample to powder while e'posed to the usuallaboratory atmosphere could encourage water absorption with

    consequent composition change, and is best avoided.

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    ROTATO!A" #S$O%&T&RS

    range 10 to 10(poise

    either the crucible or

    the plunger is rotated

    and the relationshipbetween the measured

    torque and the

    rotational speed gives a

    measure of the viscous

    drag exerted by the

    liquid.

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    '(&R &"O!)ATO! #S$O%&T&RS

    range 10)to 101*

    measuring the rate of extension of a glass fiber suspended vertically in asuitable furnace

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    %iber extension determines the dynamic viscosity of the glass by measuring the

    elongation of the sample under uniaxial stress, implicitly assuming that the flow

    behavior is &ewtonian.

    . %ibers are drawn with diameters between '.( and '.)mm to yield test

    samples between *' and ''mm in length

    +. Each end of the sample is fused to a bead about +mm in diameter to

    allow the sample to be suspended in the furnace and coupled to a loading

    device.

    . "ny surface layer resulting from the drawing process is removed by

    etching, and samples with visible imperfections scratches, inclusions, non$

    constant diameter must be discarded

    -. The sample is mounted as indicated linked by a wire or ceramic coupling

    to a thin vitreous silica rod which extends outside the furnace to accept the

    weights used for loading

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    The method is absolute in that the viscosity is calculated directly from

    knowledge of the sample geometry, the loading and the measured extension

    rate. #rovided that the dead weight of the fiber and the effects of surface

    tension of the glass may be neglected

    the rate of extension of the loaded fiber

    where is the dynamic viscosity, m is the mass of the system that loads the fiber,

    g is the acceleration due to gravity, lis the length of the fiber at the start of a

    measurement, l+is the length of the fiber at the end of the measurement, /dt0 is

    the time interval over which the measurement is taken, and " is the surface areaof the fiber specimen 1excluding the balls at the ends2.

    dl = l1+

    l

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    urface tension / opposes the applied stress barrier againstincreasingthe surface area of the glass when the ber elongates. o, the

    downwardforce is a balance between gravitational load and surface tension! = 234g - 5/r

    annealing point! elongation rate = .('10-6 l7d8 strain point ! rate = 0.0*16 ' rate at the annealing point

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    Fiber temperature is monitored by several thermocouples distributed

    along the length of that portion of the furnace chamber occupied by

    the sample

    3easurements may be made with the furnace temperature rising steadily or at

    constant temperature

    To limit the danger of the fibers necking and producing anomalous results, the

    total extension of one particular sample should not exceed '4 over the series

    of readings

    5ittleton softening point, which is a variation on the fiber extension method. 6ere,

    a glass fiber of specified dimensions is sub7ected to a defined constantly rising

    temperature environment and allowed to extend under its own weight. The

    measurement depends on establishing the temperature at which

    the fiber tip moves downward at a rate of mm8minute

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    (&!*!) (&A% #S$O%&T&RS

    range 109to 101(poise

    specimen in the shape of a rod or beam supported near its ends and

    loaded midway between the supports.

    beams are about mm in diameter and the distance between the

    supports is about -'mm.

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    :hen a load is applied the initial response of the sample is a rapidelastic de;ection, followed by a slower de;ection as ;ow occurs.Provided the sample is behaving in a

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    diameter of the beam is not less than about '4 of the span between the lower

    supports and when the total mid$point deflection has not exceeded about *4 of

    that span.