nanoencapsulation by interfacial polymerisation · 2 agfa-gevaertgroup • founded in 1867, ipo in...
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Nanoencapsulation by Interfacial Polymerisation
Lionel PettonInnovations in Encapsulation 2017
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Agfa-Gevaert Group
• Founded in 1867, IPO in 1999 (Brussels)• Headquartered in Antwerp, Belgium• Sales of EUR 2.537 billion in 2016• 10,360 employees (FTEs) worldwide• Wholly owned sales organizations in more
than 40 countries• 25 R&D and production sites around the globe• Global market leader in each of its divisions
€ 2.5 billion
Graphics
50%
HealthCare
43%
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Encapsulation at Agfa-Gevaert
• An old history to build upon: First patents filed in 1962
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Encapsulation Methods
Rao, J. P.; Geckeler, K. E., Progress in Polymer Science 2011, 36 (7), 887-913.
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Patent Landscape
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PatBase Search (1/12/17): *encapsulation and (interfac* w1 polymeri?ation)
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International Patent Classification (IPC): Application Fields
Pharmaceuticals
Organic fine chemistry
Biotechnology
Basic materials chemistry
Chemical engineering
Analysis of biological materials
Textile and paper machines
Optics
Macromolecular chemistry, polymersAudio-visual technology
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Encapsulation: Interfacial Polymerisation• Advantages:
• Good encapsulation degree• Can obtain a shell from a polymer not soluble in common
solvents• Crosslinked capsules possible• Core-shell morphology
• Disadvantages:• Reactive chemistry
• Residual monomer• Not always compatible with ingredients to be encapsulated
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Encapsulation: Interfacial Polymerisation
InterfacialPolymerisation
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Encapsulation: Interfacial Polymerisation
• Process:
1. Oil phase: • Active product• Monomer (e.g. isocyanate)• Solvent (e.g. ethyl acetate)
2. Emulsification:• Oil in water (O/W)• Dispersing agent(s)
3. Solvent evaporation
4. Interfacial polymerisation
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Nanoencapsulation
• Often in literature Microcapsule = Nanocapsule• 1 µm < Microcapsules < 100 µm• 1 nm < Nanocapsules < 1 µm (EU definition: nano < 100 nm)
• Why nanoencapsulation?• System constraints• Optical properties
• How?• Intensive emulsification process• High dispersing agent concentration
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Laser Marking
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Laser Marking: Concept
Capsule containing a leucodye (furan dye):
Developer: Acid (e.g. zinc 3,5-bis(a-methylbenzyl) salicylate).Infrared Absorber: e.g. carbon black or cyanine dye
Substrate Substrate
1064 nm
DEVELOPER
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Laser Marking: Capsules
Capsule shell formed by interfacial polymerisation:
isocyanate + amine → polyurea shell (linear or cross-linked)
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Laser Marking: Capsules
InterfacialPolymerisation
Organic phase:
- Leuco dye(s)- Isocyanate(s)
(e.g. TakenateD120N)
- Additives (e.g. UV absorber)
- Solvent (e.g. EtOAc)
Water phase:
- Water- Polyvinyl Alcohol
Water phase:
- Amine (e.g. pentamine)
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Laser Marking: Capsules
Leuco dye
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Inkjet Inks
Medium
Binder
Pigment
Additives
Ink
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Inkjet Inks
• Print head nozzle → 20 – 50 µm diameter• Low viscosity → 1 – 15 mPa.s at jetting temperature• Colloidal stability and rheology critical
Print head nozzle Ink Jetting
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Inkjet Inks: Self-Dispersing Capsules
• Core: Blocked isocyanate
• Improved ink adhesion after thermal treatment (100 °C –160 °C):
• Capsule breaks-up• Reactive isocyanate generated in-situ
thermal activation
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Inkjet Inks: Self-Dispersing Capsules
• Shell• Self-dispersing: reactive surfactant copolymerised with isocyanate
• High colloidal stability:
M+
M +
M+
M+
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Encapsulation by Interfacial Polymerisation
A versatile tool
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Thanks
• Fabienne Goethals• Johan Loccufier• Amandine Ligot
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