Product Design For Plastic Technology

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    PST66

    Principles of Product Design

    Teaching Methodology: Lecture

    Course Work : 60%

    Final examination 2-hour paper: 40%

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    PST66

    Principles of Product Design

    References

    Morton-Jones, D.H.and Ellis, J.W., Polymer

    Products , Chapman and Hall.

    Lockett, F.J., Engineering Design Basis for

    Plastics Products, HMSO

    Malloy, Robert A.,Plastics Part Design forInjection Molding: An Introduction,,(1994)

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    PST66

    Principles of Product Design

    Product design consideration; from the concept of design

    to the drawing of selected design in view of the product

    application and functionality.

    Selection of appropriate materials according to design,manufacturing and cost of production.

    Analysis of the preliminary designs for uniformity of

    section thickness, strength and assembly.

    Mechanical behaviour for structural designs; Stress analysis for polymers, dynamic and cyclic loading,

    static loading and stiffness.

    Designing for quality,

    Function, production, economics, rigidity and toughness

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    PST66

    Principles of Product Design

    Mould design :Sprue, runner and gate designs.

    Design for manufacturability

    Mould filling, shrinkage, warpage and tolerances

    Design for assembly

    Screw fittings, press fit, snap fit, metal inserts

    Welding of plastic products

    Hot gas, hot plate, friction, electric resistance, magnetic

    induction, radio frequency (microwave) and ultrasonic

    Decoration in plastics

    Self colouring, marbling effects, painting, metallization, hot

    and mould foiling and printing

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    Concept of Design to the Drawing of Selected Design in

    View of the Product Application and Functionality

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    Selection of Appropriate Materials According to Design,

    Manufacturing and Cost of ProductionMake Molding Simple

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    Selection of Appropriate Materials According to Design,

    Manufacturing and Cost of Productionheat vs density of melt

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    Selection of Appropriate Materials According to Design,

    Manufacturing and Cost of Productionheat vs density of melt

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    Selection of Appropriate Materials According to

    Design, Manufacturing and Cost of ProductionMelt at Rest vs During Flow

    Polymer chains are forced tochange from their random coilstate to an elongated coil

    The degree of elongation/alignment is dependent on thenature of polymer and shearrate

    Shear rateis dependent on the

    channel dimensionDecrease of channel dimensionwill increase the shear rate

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    Shear rate - min max

    Low orientation

    High orientation

    tensi le forc e tensi le forc e

    Selection of Appropriate Materials According to

    Design, Manufacturing and Cost of ProductionMolecular Orientation

    Molecular orientation is caused by shear flow

    The high amount of shear inside the frozen layer, produce

    high orientation

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    Selection of Appropriate Materials According to Design,

    Manufacturing and Cost of Productionorientation vs nisotropy

    Molecular Orientationcaused by

    weak/strong anisotropy depending

    on the direction of orientation

    The difference in anisotropy caused

    Shrinkage to occur.Shrinkage is greater in the flow

    direction (orientation)than in the

    cross direction (transverse)

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    Summary

    Flow Patterns

    Orientation

    Shrinkage

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    Selection of Appropriate Materials According to Design,

    Manufacturing and Cost of ProductionCOMPENST ION FOR SHRINK GE

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    Orientation that are Frozen

    Stressthat weaken product and causes

    failure at lower applied stress levels. This

    caused cracks to propagate in the direction

    of floweasily. This can also leads todimensional instability

    However, when heat is applied, it inducesmolecular relaxation which produces

    warpingor distortions.

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    Frozen orientation (cont)

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    Frozen orientation (cont)

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    Pseudo Plastic Flow behaviour

    Orientation Extension Deformation Destruction

    of Aggregates

    Liquid not sheared

    Liquid sheared

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    (Dynamic)Viscosity h

    Shear stress t

    Shear/deformation gShear rate g

    t = h * g

    y

    A

    F

    A

    [ = Pa]Nm2

    g =dxdy

    [ = ]1s

    m

    s * mg =dvdy

    =dg

    dt

    v,F

    x

    .

    .

    .

    Area A Force F

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    Dynamic viscosity h[Pas]

    t

    = shear stress [Pa]

    g= shear rate [1/s]

    1 Pas = 1000 mPas

    1 mPas = 1 cP (centi Poise)

    Kinematic viscosity n[mm2/s]

    = density [kg/m]

    1 mm/s = 1 cSt (centi Stokes)

    h

    =n

    g

    t=h

    .

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    Newtonian Flow Behaviour

    0 5 10 15 20 25 30 35 40 45 50

    [1/s]

    0

    50

    100

    150

    200

    250

    300

    350

    400

    450

    500

    [Pa]

    1

    10

    100

    [Pas]

    Flow curve

    Viscosity curve

    .

    Constant Proportionality between Shear Stress and Shear RateViscosity remains constant

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    0 50 100 150 200 250 300 350 400 450 5000

    20

    40

    60

    80

    100

    120

    0.1

    1.0

    Flow Curve

    Viscosity Curve

    [1/s].

    [Pas]

    [Pa]

    At constant time, if viscosity decreaseswith shear rate

    SHEAR THINNING

    Non Newtonian Behaviour of Plastics

    Shear Rate Dependent

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    0 50 100 150 200 250 300 350 4000

    500

    1000

    1500

    2000

    2500

    3000

    1

    10

    Non Newtonian Behaviour of Plastics

    Shear Rate Dependent

    Flow Curve

    Viscosity Curve

    .

    [1/s].

    [Pas]

    [Pa]

    At constant time, if viscosity increaseswith shear rate

    SHEAR THICKENING

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    At constant shear rate,if viscosity

    Decreases with time :THIXOTROPYIncreaseswith time : RHEOPEXY

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    Heating and Cooling

    Problems:

    Dimensional Tolerance Internal Stresses

    Dimensional Stability During Service

    Plastics has a high thermal expansion and contraction

    Coefficient of linear expansion,

    = expansion / (original length x temperature rise)

    Coefficient of cubical expansion,

    = 3

    The expansion of the material per degree rise in temperature

    Typically a 1000C rise in temperature produces an increase

    between 0.005 and 0.2 mm/mm depending on the material grade

    and the molding conditions

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    Shrinkage

    Excessive decrease in dimension in a part after processing or cooling

    Typically due to:

    Temperature gradient

    Rate of cooling Pressure during shaping

    Anisotropy due to orientation

    Amount of crystals

    Semi crystalline Vs Amorphous

    PS do not shrink in comparison to PE

    Degree of coolingPET can produce up to 50% crystallinity

    when cooled rapidly

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    Shrinkage (cont)

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    Shrinkage (Rectify)

    Inside Mould

    Adjust the mould temperature. A cold mould solidifies and forms aplastic skin sooner than a hot mould, resulting in a shrinking of plasticbefore full injection pressure is applied. However, a hot mould allowspolymer melt to continue to move and be compressed by injectionpressure before solidifying.

    Typically, a 10%change in mould temperature can result in a 5%change in original shrinkage.

    Inside Barrel

    Adjust the barrel temperature while plastic resides in the barrel

    In general, the higher the plastic temperature, the greater the amount

    of shrinkage.This is because of the increase in activity (expansion ofmolecules) of the individual plastic molecules as the temperaturerises.

    Typically, shrinkage rates can be changed 10 % by changing barreltemperatures 10 %

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    Shrinkage (cont)

    Minimize by:

    Incorporation of fillers

    Thermal expansion of the plastics lowered.

    However, fillers may affect dimensional

    stability and produce anisotropy

    Optimise mould/melt temperature, reduce

    variation in temperature Reduce variation in wall thickness.

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    Warpage

    Moulded part is twisted or bent from the intended shape

    after ejection.Common in thin walled containers and large

    flat moulded parts

    Some possible cause:Differential shrinkage within component

    Remedies, to check:

    Mould temperatures for both halves of the mould

    Injection rate- may be too slow (or too fast). Mould cooling - avoid differential cooling

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    Warpage

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    Warpage

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    Part Shrinkage Versus Mould

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    Part Shrinkage Versus Mould

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    Temperature and Rheology

    On application of heat, molecules vibratesand mobility increased

    Viscosity, for at given polymer melt at different temperaturesaresuperposable by shift at constant stress

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    Temperature and Rheology

    Viscosity is lower at high temperatures

    The elastic modulus of polymers is less sensitive to temperature change

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    Table compares the Relative Fluidity Index value (RFI) at different temperatures for different polymers

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    Due to Non-Newtonian character of the polymer melts, superposition offlow curves at produces temperatures shiftat constant stress.

    The viscosity dependence on temperature decrease at high shear rates

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    Importance of Temperature Monitoring in Rheology

    In polymer processing, high temperature is expensive

    More energy is required to raise the temperature.Time necessary to cool the material to form a stable

    product.May lead to decomposition

    Thus, in practice we usually seek to process in thelowest temperature in which the temperature willincrease with work output

    Hence, if material can be softened by heat input early inthe process, then non-uniform heat generation can beavoided at the later stage in the processing

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    Effects of Pressure Pressure reduces both free volume and molecular mobility so leading to an

    increase in viscosity

    The influence of pressure on viscosity is qualitatively similar but opposite insign to that of temperatures.

    ressure may be considered as the negative of temperature

    The application ofP (differential pressure) increases the viscosity;T is the differential temperature rise viscosity

    ( T / P) where = viscosity

    However instantaneous temperature rise, T resulting from theinstantaneous pressure, P.( T / P) s,

    where s is the entropy which is a measurement of disorder.

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    The correlation suggests that if no direct measure of the influence of pressureon viscosity is available, then the thermodynamic function may be used as aguide.

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    In polymer processing, the combination of high pressure and lowtemperaturewill tend to promote the crystallizationof some materials sothat in some cases, the harder one pushes, the less the material

    will flow.

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    Sinking

    Depressionin a moulded product caused by

    shrinking or collapsing of the resin during cooling.

    Main cause: As the resin changes from a molten state to a

    solid state, it occupies a smaller volume (this iscalled shrinkage). As more and more of themolten resin solidifies a vacuum is formed in thethicker sections and this tends to pull the surfaceof the moulding inwards and forms a depressioncalled a sink mark

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    Sinking

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    Sinking

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    Ways to Reduce Sinking

    Hold-on pressure - too low

    Hold-on pressure time - too short

    Mould temperature - too low.

    Gateincrease in gate number

    Part sectiontoo thick

    Incorporate fillers

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    Thick sections

    When moulding thick sections, the surfacelayer becomes hotter than the interior layers

    Due to poor conductionof the polymersexpansion on the surface is g reater than theinter iorhence developing differentialexpansion

    Requires the removal of heat efficiently, thusmore energy needed for cooling

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    Uniform Wall Thickness

    Constant wall thickness or gradual transition between thickan thin wall section

    Ratio of thick to thin is 3: 1.

    All surfaces perpendicular to the parting lines are tapered to

    assist ejection of the components from the mould

    Any abrupt changes to flow leads to internal stresses anddifferential thermal gradient.

    These stresses can lead to an area of tension and

    compression that will result in warping and fracture. However,the thermal stresses can be reduced by annealing duringmoulding or post moulding.

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    Corners

    Two walls adjoin andinterrupt the smooth flow

    of melt.

    Set up internal stresses,

    especially with fiber

    reinforced materials

    Act as notched which

    encourages failure

    Should be designed with

    the radius rounded

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    Part Thickness and Corners

    Range 0.5 mm to 4 mm(0.02-0.16in), dependent

    on the part design and

    size.

    A molded piece shouldhave uniform thickness

    throughout

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    Corners

    Bosses

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    BossesBosses are used for mounting/fasteningpoint purposes

    or to serve as reinforcement around holes

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    Boss

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    Boss

    To support moulded parts or studs for assembling

    components.Metal inserts should not have sharp

    corners and boss must sink into the inserts on

    cooling because of higher coefficient of plastics

    Can be incorporated via ribsat corners or along theside of the wall

    Ejector pin must be incorporated at the base of

    each boss at the cavity side cavity to facilitate

    extraction. This also allows air to escape, thusavoid burn mark on the surface and incomplete

    filling

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    Boss

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    Weld line

    HEAD ONof 2 flow front

    Multi gating system

    Caused local weakness

    Inconspicuous areas

    PARALLEL FLOW of 2

    flow front

    Flow around pins

    Caused local weakness

    Inconspicuous areas

    Melt line

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    Weld lines

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    Weld lines

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    Designing for Stiffness

    Resist deflection under bending load; deflection (Y)

    is inversely proportional to the stiffness factor(1 / ( E I ))

    Two ways of resisting Y

    select material with high E

    select a suitable cross section geometry & design, I

    Important :

    shear ( torsion) forces and deformation must be

    considered as a cross section may have highresistance to bending but not necessarily totorsional shear

    Reinforcing ribs

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    Reinforcing ribs Effective way to improve the rigidity and strength

    Save material and weight

    Shorten molding cycles and eliminate heavy crosssection

    Disadvantage, may produce warpage and stress

    concentration

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    Analyzing Defects

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    Chart of Defects