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Supramolecular Arrest and Activation
for the Network formation of Acid
Catalyzed Epoxy Polymerization
Matthew J. Spencer, James V. Crivello, Chang Y. Ryu
Department of Chemistry and Chemical Biology, Rensselaer Polytechnic Institute
Motivation
• Epoxy network formation triggered by
– Hardening Agent
– Acid generation with UV
• Develop a one component system that cures
quickly at low temperatures yet has RT stability
– Supramolecular chemistry
Matthew J. Spencer, James V. Crivello, Chang Y. Ryu
System
• Super Acid Generation by Onium Salts
– Photo-initiation
– Redox-initiation
• Polymerizations monitored by
– Optical Pyrometry
– Rheology
Matthew J. Spencer, James V. Crivello, Chang Y. Ryu
Ar2I+
MtXn
-
h
Ar2I+
MtXn
-
* ArI+
MtXn
-
+ Ar
Ar+
MtXn
-
+ ArI
. .
HMtXn
k1
10
30
50
70
90
110
130
150
170
190
0 20 40 60 80 100 120 140 160
Temperature(oC)
Irradiation Time (s)
O
O
OO
1M%
O
O
O
O
O O
O
O
O
O
O
O
OO
O
2620 mJ/cm2
Matthew J. Spencer, James V. Crivello, Chang Y. Ryu
3,4-epoxycyclohexylmethyl
3’,4’-epoxycyclohexane
carboxylate
Ring Opening Polymerizations
• Highly exothermic due to ring strain
Matthew J. Spencer, James V. Crivello, Chang Y. Ryu
10
30
50
70
90
110
130
150
170
190
0 20 40 60 80 100
Time (s)
Temperature(o
C)
O
O
O
O
O
2700 mJ/cm2
I+
O n-C11H23
SbF6
-
Supramolecular Arrest though Monomer Design
• Alkyl glycidal ethers have long induction periods
• Increasing coordination by the monomer
O
O
+
O
O
O
O
H
Matthew J. Spencer, James V. Crivello, Chang Y. Ryu
Neopentlyglycoldicly
cidyl ether Trimethylolpropane
triglycidyl ether
Methyl
glycidyl
ether
Dynamic Shear Rheology
Matthew J. Spencer, James V. Crivello, Chang Y. Ryu
G* = G’ + iG’’
δ = atan(G’’/G’)
Dynamic and Steady Shear Experiments
Dynamic
Steady
Model Compound
Dipropylene Glycol Dyglicidal Ether
Matthew J. Spencer, James V. Crivello, Chang Y. Ryu
Modifying Reaction Kinetics with Crown Ethers
18-crown-6
1050 mJ/cm2
Matthew J. Spencer, James V. Crivello, Chang Y. Ryu
10
30
50
70
90
110
130
150
170
190
0 20 40 60 80 100 120 140 160
Temperature(oC)
Irradiation Time (s)
O
O
OO
1M%
O
O
O
O
O O
O
O
O
O
O
O
OO
O
2620 mJ/cm2
Modifying Reaction Kinetics with Crown Ethers
Matthew J. Spencer, James V. Crivello, Chang Y. Ryu
Matthew J. Spencer, James V. Crivello, Chang Y. Ryu
Dynamic Shear Experiments with 15-Crown-5 at 40C
Moles IOC-11 / moles Monomer ~ 0.002
The Supramolecular Complex
• 2,6-di-t-butylpyridine is a ‘proton trap’, but will not neutralize larger
species like an tertiary oxonium ion
• Crown ethers serve as a
‘molecular ruler’ for acid species
Matthew J. Spencer, James V. Crivello, Chang Y. Ryu
Polyether ring Pore Size (A)
12-crown-4 1.2-1.5
15-crown-5 1.7-2.2
18-crown-6 2.6-3.2
Summary & Future Work
• Development of one component epoxy system
– Long working life and low temperature cure
• Control of cationic ring opening polymerizations
– Monomer Design
– Modifying reaction kinetics with crown ethers
– Crown ether size effect is observed
• Epoxy Blends
• NMR Complex Determination
Matthew J. Spencer, James V. Crivello, Chang Y. Ryu

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APS Dallas

  • 1. Supramolecular Arrest and Activation for the Network formation of Acid Catalyzed Epoxy Polymerization Matthew J. Spencer, James V. Crivello, Chang Y. Ryu Department of Chemistry and Chemical Biology, Rensselaer Polytechnic Institute
  • 2. Motivation • Epoxy network formation triggered by – Hardening Agent – Acid generation with UV • Develop a one component system that cures quickly at low temperatures yet has RT stability – Supramolecular chemistry Matthew J. Spencer, James V. Crivello, Chang Y. Ryu
  • 3. System • Super Acid Generation by Onium Salts – Photo-initiation – Redox-initiation • Polymerizations monitored by – Optical Pyrometry – Rheology Matthew J. Spencer, James V. Crivello, Chang Y. Ryu Ar2I+ MtXn - h Ar2I+ MtXn - * ArI+ MtXn - + Ar Ar+ MtXn - + ArI . . HMtXn k1
  • 4. 10 30 50 70 90 110 130 150 170 190 0 20 40 60 80 100 120 140 160 Temperature(oC) Irradiation Time (s) O O OO 1M% O O O O O O O O O O O O OO O 2620 mJ/cm2 Matthew J. Spencer, James V. Crivello, Chang Y. Ryu 3,4-epoxycyclohexylmethyl 3’,4’-epoxycyclohexane carboxylate
  • 5. Ring Opening Polymerizations • Highly exothermic due to ring strain Matthew J. Spencer, James V. Crivello, Chang Y. Ryu 10 30 50 70 90 110 130 150 170 190 0 20 40 60 80 100 Time (s) Temperature(o C) O O O O O 2700 mJ/cm2 I+ O n-C11H23 SbF6 -
  • 6. Supramolecular Arrest though Monomer Design • Alkyl glycidal ethers have long induction periods • Increasing coordination by the monomer O O + O O O O H Matthew J. Spencer, James V. Crivello, Chang Y. Ryu Neopentlyglycoldicly cidyl ether Trimethylolpropane triglycidyl ether Methyl glycidyl ether
  • 7. Dynamic Shear Rheology Matthew J. Spencer, James V. Crivello, Chang Y. Ryu G* = G’ + iG’’ δ = atan(G’’/G’)
  • 8. Dynamic and Steady Shear Experiments Dynamic Steady Model Compound Dipropylene Glycol Dyglicidal Ether Matthew J. Spencer, James V. Crivello, Chang Y. Ryu
  • 9. Modifying Reaction Kinetics with Crown Ethers 18-crown-6 1050 mJ/cm2 Matthew J. Spencer, James V. Crivello, Chang Y. Ryu
  • 10. 10 30 50 70 90 110 130 150 170 190 0 20 40 60 80 100 120 140 160 Temperature(oC) Irradiation Time (s) O O OO 1M% O O O O O O O O O O O O OO O 2620 mJ/cm2 Modifying Reaction Kinetics with Crown Ethers Matthew J. Spencer, James V. Crivello, Chang Y. Ryu
  • 11. Matthew J. Spencer, James V. Crivello, Chang Y. Ryu Dynamic Shear Experiments with 15-Crown-5 at 40C Moles IOC-11 / moles Monomer ~ 0.002
  • 12. The Supramolecular Complex • 2,6-di-t-butylpyridine is a ‘proton trap’, but will not neutralize larger species like an tertiary oxonium ion • Crown ethers serve as a ‘molecular ruler’ for acid species Matthew J. Spencer, James V. Crivello, Chang Y. Ryu Polyether ring Pore Size (A) 12-crown-4 1.2-1.5 15-crown-5 1.7-2.2 18-crown-6 2.6-3.2
  • 13. Summary & Future Work • Development of one component epoxy system – Long working life and low temperature cure • Control of cationic ring opening polymerizations – Monomer Design – Modifying reaction kinetics with crown ethers – Crown ether size effect is observed • Epoxy Blends • NMR Complex Determination Matthew J. Spencer, James V. Crivello, Chang Y. Ryu

Editor's Notes

  1. Structural AdhesivesPolyfuctionalepoxide and polyamine hardening agentProblems with homogeneity, reaction begins upon mixing
  2. Photo polymerization is simple but limited in its applications. Thickness of sample limited by penetration depth of light.Optical Pyrometry uses inferred camera to monitor temperature of reaction.Rheometer can measure viscosity and elasticity and use these to establish the onset of crosslinking
  3. Increased reactivity with 18 crown, complete suppression with 12 crown
  4. OP is well suited for highly exothermic reactions like ring opening polymerizations.Temperature is show to be related to % converstion for initial portion of graph
  5. Descrbe dynamic shearComplex dynamic modulusG’ the elastic modulusG” the viscous modulous
  6. Just under 2 hours at 25C and under 3 minutes at 60CSteady shear provides method for in-situ mixing.Agreement of steady and dynamic indication of acid dispersion
  7. Increased reactivity with 18 crown, complete suppression with 12 crown
  8. Crown is 10-20M% of monomer