2
and Micro Injection Molding Compression Induced Solidification The concept developed at the Institute of Polymer Technology (LKT) is based on simultaneous solidification of the hot melt in the whole cavity solely by pressure. Thereafter, the compressed and solidified melt is cooled down (Fig. 1). The separation of the parallel processes of cooling and solidification during polymer processing is made possible by the pressure- dependent glass transition temperature range of polymers, which shifts to higher temperatures with higher pressure. At the time of solidification, i.e. when the glass transition is exceeded due to the pressure level, the component is subjected only to the significantly lower coefficient of expansion of the solid state. This single-phase cooling minimizes effects due to locally different shrinkage coefficients. The technique leads to better dimensional accuracy and homogeneous inner component properties (Fig. 2 and Fig. 3). Process Strategy At the beginning of the process, the mold cavity with dynamic temperature control is set to a temperature higher than the glass transition temperature of the polymer and is filled with melt. Subsequently the melt cools down to mold temperature in the cavity. A pressure is then applied to the melt, which is so high that the mass is solidified by falling below the vitrification line (glass transition). The dynamic mold temperature control is then used to cool down the solidified component to demolding temperature while remaining a constant cavity volume or constant pressure. The compression causes an adiabatic temperature increase, which makes it necessary to adjust the pressure in order to achieve solidification, i.e. to exceed the freezing line. Optical lenses often exhibit large varying component thicknesses, which is why they cannot be produced with conventional polymer processing techniques. In the standard processing methods for polymers, sink marks and internal inhomogeneities such as residual stresses and density variations occur due to the simultaneous presence of the solid and the molten state during cooling (Fig. 1) and their varying coefficients of expansion. Compression induced solidification (CIS) provides the possibility to reduce or even avoid these undesirable component defects. Compression Induced Solidification Solidification by pressure Motivation Fig. 3: Photoelastic image with circular polarized light, component thickness: 18 mm a) Reduced internal stresses of a component produced via CIS b) Compared to an injection molded component Fig. 2: Dimensional deviation of the component from the mold b) Solidification of the melt via pressure and subsequent cooling during CIS Fig. 1: a) Different phases of the polymer (liquid and solid) during standard injection molding Liquid T [°C] Compression temperature: 190 °C Material: Polycarbonate Dimensional deviation from the mold [mm] Compression pressure [bar] 0.00 -0.05 -0.10 -0.15 400 600 800 1000 1200 1400 Reference sample: injection molding T [°C] 170 110 50 Solid a b Liquid Solid Solid Liquid Solid Solid a b 10 mm 10 mm Barcode zu Ansprech- partner und Infomaterialien

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Page 1: Compression Induced Solidification and Micro Injection Molding

and Micro Injection MoldingCompression Induced Solidification

The concept developed at the Institute of Polymer Technology

(LKT) is based on simultaneous solidification of the hot melt in

the whole cavity solely by pressure. Thereafter, the

compressed and solidified melt is cooled down (Fig. 1). The

separation of the parallel processes of cooling and solidification

during polymer processing is made possible by the pressure-

dependent glass transition temperature range of polymers,

which shifts to higher temperatures with higher pressure. At the

time of solidification, i.e. when the glass transition is exceeded

due to the pressure level, the component is subjected only to the

significantly lower coefficient of expansion of the solid state.

This single-phase cooling minimizes effects due to locally

different shrinkage coefficients. The technique leads to better

dimensional accuracy and homogeneous inner component

properties (Fig. 2 and Fig. 3).

Process StrategyAt the beginning of the process, the mold cavity with dynamic

temperature control is set to a temperature higher than the glass

transition temperature of the polymer and is filled with melt.

Subsequently the melt cools down to mold temperature in the

cavity. A pressure is then applied to the melt, which is so high

that the mass is solidified by falling below the vitrification line

(glass transition). The dynamic mold temperature control is then

used to cool down the solidified component to demolding

temperature while remaining a constant cavity volume or

constant pressure. The compression causes an adiabatic

temperature increase, which makes it necessary to adjust the

pressure in order to achieve solidification, i.e. to exceed the

freezing line.

Optical lenses often exhibit large varying component

thicknesses, which is why they cannot be produced with

conventional polymer processing techniques. In the standard

processing methods for polymers, sink marks and internal

inhomogeneities such as residual stresses and density

variations occur due to the simultaneous presence of the solid

and the molten state during cooling (Fig. 1) and their varying

coefficients of expansion. Compression induced solidification

(CIS) provides the possibility to reduce or even avoid these

undesirable component defects.

Compression Induced Solidification

Solidification by pressure

Motivation

Fig. 3: Photoelastic image with circular polarized light,

component thickness: 18 mm

a) Reduced internal stresses of a component

produced via CISb) Compared to an injection molded component

Fig. 2: Dimensional deviation of the component from the mold

b) Solidification of the melt via pressure and

subsequent cooling during CIS

Fig. 1: a) Different phases of the polymer (liquid and solid)

during standard injection molding

Liquid

T [°C]170 140 110 80 50 20

Compression temperature: 190 °CMaterial: Polycarbonate

Dim

ensi

onal d

evi

atio

n f

rom

the m

old

[m

m]

Compression pressure [bar]

0.00

-0.05

-0.10

-0.15400 600 800 1000 1200 1400

Reference sample: injection molding

T [°C]

170 110 50

Solida b

Liquid Solid

Solid

Liquid Solid

Solid

a b

10 mm 10 mm

Barcode zuAnsprech-partner und Infomaterialien

Page 2: Compression Induced Solidification and Micro Injection Molding

Motivation

Potentials of Dynamic TemperingBased on gears made of Polyoxymethylene (POM), Fig. 4

shows the influence of the mold temperature on the formation of

the morphology and the required cycle time. For technically

challenging components, a cavity temperature of 100 °C is

common. A resulting skin layer can only be avoided by

increasing the temperature to 140 °C. Therefore, the required

longer cooling phase doubles the cycle time for the tested gear-

wheel. Using a dynamic temperature control, injection can take

place at a high mold temperature at the level of the

crystallization temperature of ~ 150 °C (POM). Mold and part are

simultaneously cooled down at high cooling rates leading to a

possible eject after a total cycle time of less than 20 s.

Components with Locally Different PropertiesIn addition to influencing the crystalline structure of the entire

component, current research at LKT deals with the development

of a new mold system which allows for local heating using seg-

mented heating ceramics. Therefore, different mold tempera-

tures within one cavity can be realized to manufacture compo-

nents with locally different properties. Results for studying the

morphological characteristics (Fig. 5) correlate well with the

resulting mechanical properties (Fig. 6). Injection molded

Polyamid 6 microplates show that it is possible to generate com-

ponents with locally varying properties (which can be attributed

to the different sizes of the crystalline structures) by choosing

different temperature cavity areas. Besides achieving an

increase in the degree of crystallization, an increase in the ten-

sile modulus by the order of 30 % can be reached.

Micro Injection Molding

In the field of micro and thin-wall technology, injection molding

has become the method of choice for producing components at

a very high technical level. Nevertheless, the potential of most

common semi-crystalline thermoplastics is usually not fully

utilized. The main reason for that is the used cooling strategy.

With increasing ratios of surface to volume at the transition from

large to small and thin geometries, an increased heat loss

through the mold wall occurs. The associated differences in

thermal history lead to a change in internal structure associated

with changes in component properties. Hence, a thorough

process control is vital in injection molding. An increase in mold

temperature can improve the crystallization for semi-crystalline

polymers, which might lead to a higher stiffness and strength

while reducing the elongation at break. Since the main areas of

application for polymer micro parts are medical technology,

movable components of optical systems, micro gears in micro

fluidics, biotechnology and electronics or micro electro-

mechanical systems, the tribological behaviour of such

components is also of particular interest. Thus, the improved

crystallinity as a result of the increased mold temperature can

lead to a decrease in wear and an increase in the allowable

number of load cycles for gears, while the friction behavior

remains unchanged.

- Thermoplastic micro injection molding

- Viscosity measurements with high pressure capillary

rheometry

- Structural analysis of semicrystalline microparts

- Stress optical images of amorphous components

Research Objects and Service for Industry

Fig. 6: Tensile modulus and tensile strength of an injection

molded component manufactured at different mold

temperatures

- Process related cooling rates with Fast Scanning

Calorimetry (FSC)

Fig. 5: Morphology of an injection molded component

manufactured at different mold temperatures

Fig. 4: Influence of the mold temperature on the resulting

morphology and cycle time of an injection molded gear

wheel

| https://www.lkt.tf.fau.eu/

| Institute of Polymer Technology | Am Weichselgarten 9 | 91058 Erlangen-Tennenlohe, Germany| Phone: +49 9131 85-29700 | Fax: +49 9131 85-29709 | Mail: [email protected]

0

20

40

60

80

100

135

Tensile modulus

Tensile strength

Tensi

le m

odulu

s E

[N

/mm

2 ]t

2Te

nsi

le s

trength

R[N

/mm

]m

Mold temperature T [°C]m

1000

1500

2000

2500

3000

3500

4000

500

0190

200 µm 200 µm 100 µm200 µm

Homogenousmorphology

Cycle < 20 s

Homogenousmorphology

Cycle > 50 s

Inhomogenousmorpholoy

Cycle ≈ 27 s

100 °C

Mold temperature 140 °C

Variothermal (150/70 °C)

50 µm

Mold temperature Tm

[°C]

135 190

50 µm

300 µm 300 µm 300 µm