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Novel Method for Rapid
Determination of Thermoformability
Dr. Amit Dharia
Transmit Technology Group, LLC, TX
Dr. Don Hylton
McConnell Co. Inc., GA
Outline
® Properties –Thermoforming Process
relationship
® Current test methods
® Description of new test apparatus
/operation/ data acquisition
® Application and data interpretation
® Future plans
® Conclusion
Thermoforming Process
® Extruding sheet stock
® Heating sheet above Tg
® Stretching heated sheet in rubbery state
® Forming stretched sheet
® Cooling
® Trimming
® Finishing –painting, printing
Structure - Properties -
Thermoformability
® Rate of change of strength with the
change in strain rate at forming
temperature
® % Crystallinity – Breadth of rubbery
Plateau
® Molecular weight, Molecular weight
distribution, molecular architecture
(branching, crosslinking) – MFR, Melt
Elasticity
Other parameters
® Density - % filler, type of fillers, degassing
® Geometry – Thickness, area, multi-layered
structures, adhesion between layers
® Residual stresses between and within in
extruded layer sheet stock
® Thermal diffusivity (Cp, K. Rho)
® Extrusion quality ( gels, unmelts,
thickness variation, grain patterns)
® Color (IR absorption)
Current tests
® Low shear melt viscosity (MFR, RMS)
® Hot tensile test (2 in gauge length, 0.2 to 20
ipm, or 0.002 to 0.33 1/s vs. 10/1s for TF
process)
® Melt Tension (Draw Force –Melt strength,
Break Velocity –Draw down)
® Sag Test (sag distance, sag time)
® Hot Creep Test
® DMA (Relaxation time)
Major disadvantages of current
methods
® Most tests are conducted in melt or near melt
phase – TF at Tg + 30-40 F
® Specimen do not reflect actual test geometry
(shape, size, thickness clamping mode)
® Do not account for orientation, thermal stresses,
thickness variations
® Isothermal environment, does not account for
transient nature during heating/ cooling steps
® Effects of secondary process parameters can not
be evaluated
® Results cannot be directly used.
What we want to know?
® Will this material thermoform?
® Will this new material process the same?
® Will this lot process the same as the last one?
® Why this lot does not process the same?
® How much time is needed to heat the sheet?
® How fast material will heat?
® What is the right forming temperature range?
® Will melt adhesion between layers survive
heating and stretching step?
® Will material discolor, fed or degrade during
heating?
What processors want to
know?
® What is the maximum draw down ratio?
® How fast part can be made?
® What is the MD and TD shrinkage?
® Will material tear?
® How much regrind can I use?
® Will grains retain shape and depth?
® Does extruded sheet have gels or
unmelts?
What Industry Needs?
® A standard test method which reflects all unit
steps – heating, 3D stretching, forming, and
cooling
® A test equipment which can be precisely
controlled, is rapid, easy to use, provides
repeatable and quantitative information, using the
lease amount of material.
® Easy to use “Thermoformability Index” standard
for comparing, contrasting effects of selected
process/ material variables
TECHNOFORM TM
Patent PendingTTG
TECHNOFORM
Typical Data input
® Mode of operation – Plug, vacuum, vacuum +plug
® The heating element distance from the sheet
surface
® The heating element temperature
® The sheet temperature
® Heat Soak time at given temperature
® Plug velocity (2 to 400 mm/second)
® Plug Delay Time
® Plug Temperature
® Cooling time
Typical user Input Screen
Sag Distance
Thinning
Strain
hardening
Forming Depth mm
Thermoformability Index=
slope
Typical Data Output
® Heating rate (Delta C/ time)
® Sag distance
® Forming force (Stress) vs. forming
distance (strain)
® Forming Force vs. time
® Yield force
® Forming force vs. actual temperature
® Shrinkage
Heating rates for various plastic materials
(Heater at 600 C, 3” from upper, 2” from lower)
30
80
130
180
230
0 20 40 60 80
t (seconds)
T(c)
PP
HDPE
HIPS
PVC
ABS
Acetal
PMMA
Nylon
Effect of Crystallinity
0
5
10
15
20
25
30
50 70 90 110 130
Forming distance, mm
Force(N)HDPE PP HIPS PETG ABS PMMA PVC
Effect of Forming Temperature
0
2
4
6
8
10
12
14
125 145 165 185
Temperature (C)
Force(N)
ABS
PP
HDPE
HIPS
PETG
PMMA
ACETAL
Force100 = f (T, V, material)
® F(ABS) =9.2348 -0.0547 T (R2 =99%)
® F(PMMA)=7.1587 -0.0341 T(R2=98%)
® F(PETG)=10.096 -0.0601 T (R2=92%)
® F(HIPS)=9.6782 - 0.0503T(R2=93%)
® F(HDPE)=5.2771 -0.0266 T (R2=86%)
Comparison of Acetal, Nylon, TPO
0
1
2
3
4
5
6
0 50 100 150
Time (seconds)
Formingdistance(mm)
Delrin (206)
PA (241 C)
TPO (161 C)
Effect of forming Speed on HDPE @ 150 C
Effect of Forming Speed on HDPE
0
2
4
6
8
10
0 50 100 150
Distance (mm)
Fromingforce(N)
20 mm/sec
30 mm.sec
50 mm/sec
Comparison of filled vs. HMS-TPO
0
10
20
30
40
50
0 20 40 60 80 100
Distance (mm)
Force(N)
40HMSTPO 20HMSTPO
40 FTPO 20FTPO
Effect of adding HMSPP in PP
0
1
2
3
4
5
6
7
40 60 80 100 120 140
Form ing Dist ance, mm
FormingForce,Lbf
10%H MSPP 20%HMS PP 30% HMSPP
0
1
2
3
4
5
6
7
40 60 80 100 120 140
Form ing Dist ance, mm
FormingForce,Lbf
10%H MSPP 20%HMS PP 30% HMSPP
0
1
2
3
4
5
6
7
40 60 80 100 120 140
Forming Distance, mm
FormingForce,Lbf 10%HMSPP 20%HMSPP 30%HMSPP
Formability of HMSPP/PP Blends
0
2
4
6
8
10
12
10 20 30
%HMSPP
thickness(High/Low)
Effect of % Regrind on formability TPO
20% regrind / Five Successive Extrusions
0
1
2
3
4
5
6
40 60 80 100 120
Forming Distance, mm
FormingForce,Lbf
1st
2nd
3rd
4th
5th
Comparison of Test Methods
Relaxation Time (s) Vs. Force @ 75 mm depth
R2
= 0.9968
0
2
4
6
8
10
12
0 2 4 6 8
Relaxation Time (sec)
FormignFroce(75mm)
PP, 165 C
HDPE,140C
HIPS,160 C
Future Plans
® Develop a standard “Thermoformability
Index” similar to Melt Flow Index; which
can be used by industry as specification
to describe thermoformability of material.
® Refine force-vs. displacement data into
stress vs. strain data for each plug
geometry
® Develop an integrated predictive modeling
system like “Moldflow”.
Conclusions
® A novel and simple test equipment is
developed which closely reflects all four
unit steps of the typical thermoforming
process and generates quantitative and
repeatable information.
® The test data can be used in raw form to
compare or contrast various materials and
process parameters input or can be
further modeled as a design or predictive
tool.

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Novel method

  • 1. Novel Method for Rapid Determination of Thermoformability Dr. Amit Dharia Transmit Technology Group, LLC, TX Dr. Don Hylton McConnell Co. Inc., GA
  • 2. Outline ® Properties –Thermoforming Process relationship ® Current test methods ® Description of new test apparatus /operation/ data acquisition ® Application and data interpretation ® Future plans ® Conclusion
  • 3. Thermoforming Process ® Extruding sheet stock ® Heating sheet above Tg ® Stretching heated sheet in rubbery state ® Forming stretched sheet ® Cooling ® Trimming ® Finishing –painting, printing
  • 4. Structure - Properties - Thermoformability ® Rate of change of strength with the change in strain rate at forming temperature ® % Crystallinity – Breadth of rubbery Plateau ® Molecular weight, Molecular weight distribution, molecular architecture (branching, crosslinking) – MFR, Melt Elasticity
  • 5. Other parameters ® Density - % filler, type of fillers, degassing ® Geometry – Thickness, area, multi-layered structures, adhesion between layers ® Residual stresses between and within in extruded layer sheet stock ® Thermal diffusivity (Cp, K. Rho) ® Extrusion quality ( gels, unmelts, thickness variation, grain patterns) ® Color (IR absorption)
  • 6. Current tests ® Low shear melt viscosity (MFR, RMS) ® Hot tensile test (2 in gauge length, 0.2 to 20 ipm, or 0.002 to 0.33 1/s vs. 10/1s for TF process) ® Melt Tension (Draw Force –Melt strength, Break Velocity –Draw down) ® Sag Test (sag distance, sag time) ® Hot Creep Test ® DMA (Relaxation time)
  • 7. Major disadvantages of current methods ® Most tests are conducted in melt or near melt phase – TF at Tg + 30-40 F ® Specimen do not reflect actual test geometry (shape, size, thickness clamping mode) ® Do not account for orientation, thermal stresses, thickness variations ® Isothermal environment, does not account for transient nature during heating/ cooling steps ® Effects of secondary process parameters can not be evaluated ® Results cannot be directly used.
  • 8. What we want to know? ® Will this material thermoform? ® Will this new material process the same? ® Will this lot process the same as the last one? ® Why this lot does not process the same? ® How much time is needed to heat the sheet? ® How fast material will heat? ® What is the right forming temperature range? ® Will melt adhesion between layers survive heating and stretching step? ® Will material discolor, fed or degrade during heating?
  • 9. What processors want to know? ® What is the maximum draw down ratio? ® How fast part can be made? ® What is the MD and TD shrinkage? ® Will material tear? ® How much regrind can I use? ® Will grains retain shape and depth? ® Does extruded sheet have gels or unmelts?
  • 10. What Industry Needs? ® A standard test method which reflects all unit steps – heating, 3D stretching, forming, and cooling ® A test equipment which can be precisely controlled, is rapid, easy to use, provides repeatable and quantitative information, using the lease amount of material. ® Easy to use “Thermoformability Index” standard for comparing, contrasting effects of selected process/ material variables
  • 12. Typical Data input ® Mode of operation – Plug, vacuum, vacuum +plug ® The heating element distance from the sheet surface ® The heating element temperature ® The sheet temperature ® Heat Soak time at given temperature ® Plug velocity (2 to 400 mm/second) ® Plug Delay Time ® Plug Temperature ® Cooling time
  • 13. Typical user Input Screen Sag Distance Thinning Strain hardening Forming Depth mm Thermoformability Index= slope
  • 14. Typical Data Output ® Heating rate (Delta C/ time) ® Sag distance ® Forming force (Stress) vs. forming distance (strain) ® Forming Force vs. time ® Yield force ® Forming force vs. actual temperature ® Shrinkage
  • 15. Heating rates for various plastic materials (Heater at 600 C, 3” from upper, 2” from lower) 30 80 130 180 230 0 20 40 60 80 t (seconds) T(c) PP HDPE HIPS PVC ABS Acetal PMMA Nylon
  • 16. Effect of Crystallinity 0 5 10 15 20 25 30 50 70 90 110 130 Forming distance, mm Force(N)HDPE PP HIPS PETG ABS PMMA PVC
  • 17. Effect of Forming Temperature 0 2 4 6 8 10 12 14 125 145 165 185 Temperature (C) Force(N) ABS PP HDPE HIPS PETG PMMA ACETAL
  • 18. Force100 = f (T, V, material) ® F(ABS) =9.2348 -0.0547 T (R2 =99%) ® F(PMMA)=7.1587 -0.0341 T(R2=98%) ® F(PETG)=10.096 -0.0601 T (R2=92%) ® F(HIPS)=9.6782 - 0.0503T(R2=93%) ® F(HDPE)=5.2771 -0.0266 T (R2=86%)
  • 19. Comparison of Acetal, Nylon, TPO 0 1 2 3 4 5 6 0 50 100 150 Time (seconds) Formingdistance(mm) Delrin (206) PA (241 C) TPO (161 C)
  • 20. Effect of forming Speed on HDPE @ 150 C Effect of Forming Speed on HDPE 0 2 4 6 8 10 0 50 100 150 Distance (mm) Fromingforce(N) 20 mm/sec 30 mm.sec 50 mm/sec
  • 21. Comparison of filled vs. HMS-TPO 0 10 20 30 40 50 0 20 40 60 80 100 Distance (mm) Force(N) 40HMSTPO 20HMSTPO 40 FTPO 20FTPO
  • 22. Effect of adding HMSPP in PP 0 1 2 3 4 5 6 7 40 60 80 100 120 140 Form ing Dist ance, mm FormingForce,Lbf 10%H MSPP 20%HMS PP 30% HMSPP 0 1 2 3 4 5 6 7 40 60 80 100 120 140 Form ing Dist ance, mm FormingForce,Lbf 10%H MSPP 20%HMS PP 30% HMSPP 0 1 2 3 4 5 6 7 40 60 80 100 120 140 Forming Distance, mm FormingForce,Lbf 10%HMSPP 20%HMSPP 30%HMSPP
  • 23. Formability of HMSPP/PP Blends 0 2 4 6 8 10 12 10 20 30 %HMSPP thickness(High/Low)
  • 24. Effect of % Regrind on formability TPO 20% regrind / Five Successive Extrusions 0 1 2 3 4 5 6 40 60 80 100 120 Forming Distance, mm FormingForce,Lbf 1st 2nd 3rd 4th 5th
  • 25. Comparison of Test Methods Relaxation Time (s) Vs. Force @ 75 mm depth R2 = 0.9968 0 2 4 6 8 10 12 0 2 4 6 8 Relaxation Time (sec) FormignFroce(75mm) PP, 165 C HDPE,140C HIPS,160 C
  • 26. Future Plans ® Develop a standard “Thermoformability Index” similar to Melt Flow Index; which can be used by industry as specification to describe thermoformability of material. ® Refine force-vs. displacement data into stress vs. strain data for each plug geometry ® Develop an integrated predictive modeling system like “Moldflow”.
  • 27. Conclusions ® A novel and simple test equipment is developed which closely reflects all four unit steps of the typical thermoforming process and generates quantitative and repeatable information. ® The test data can be used in raw form to compare or contrast various materials and process parameters input or can be further modeled as a design or predictive tool.