Microwave Fundamentals

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Presentation transcript:

Microwave Fundamentals

All of this is due to the molecular rotations created with microwaves Why Microwaves? Fast heating and curing This is the most commonly known use for heating with microwaves The least known and most powerful is the ability to lower cure temperatures Polymer curing can be performed at much lower temperatures This reduces thermal stress for adhesion and molding Internal chemical stresses are reduced in the adhesives and composites Extent of cure reactions are fully complete at these lower temperatures Evaporation of moisture and solvents efficiently at low temperatures Removal of water/solvents from resins or slurries is volumetric Fast, uniform evaporation occurs from the whole bulk Inherently selective heating allows uniquely focused processing All of this is due to the molecular rotations created with microwaves

Dipole Rotation and Heat Microwave fields excite electron distributions in molecules which cannot follow the rapid reverses in the e-field. This causes a fall in the dielectric constant (e’) and a rise in the dielectric loss factor (e”) shown in the graph below. Rapid dipole reorientation causes rotational motion and frictional heating between neighboring molecules.

Inherently Different Heating Method Heat enters from the outside-in or top-to-bottom of sample. All the molecules are heated in the whole sample instantly.

Microwaves Create Molecular Rotation Water (H2O) Methane (CH4) Dipole Moment = 1.86 D Dipole Moment = 0 D Polarizability = 1.45 Å Polarizability = 2.6 Å Even molecular groups without dipoles will rotate!

Microwave Reaction Kinetics The collision theory modified Arrhenius equation for reaction rate depends on both the collision frequency (Z) and the steric factor (r): k = Z r e (-Ea/RT) Increased molecular motion increases collision frequency (Z) Rapid re-orientation at reactive sites increases productive collisions (r) The increased reaction kinetics can be seen as either (or both) of: increased collision kinetics (Z and r) increased localized heating (energy of activation Ea) The dipoles are rotated more actively at reaction sites than in the rest of the molecule, so the bulk temperature is much lower

Selective Heating Glass & Ceramics transparent Polymer resins Silicon (doped) Metals transparent absorptive absorptive reflective + absorptive + transparent

Metal Thickness Determines Effect Metals only absorb at their skin depth thicker - reflective thinner - transparent

Practical Considerations Power dissipation: Pav = w e0 e“eff E2rms V More power is required for larger sample volumes but; Heating rate: (T – T0)/t = w e0 e“eff E2rms V/MCp °C (T – T0)/t = w e0 e“eff E2rms V/rbCp °C Heating efficiency increases with larger sample volumes. Pav = average power dissipated W = angular frequency e“eff = dielectric loss factor E2rms = electric field V = sample volume M = sample mass rb = sample density Cp = heat capacity

Heating with Molecular Rotations Molecular rotation is very efficient even in viscous materials Small water and solvent molecules evolve from resins and slurries all at once Reactions of monomers form polymers throughout the entire bulk Uniform heating is created rather than from the surface to the interior Glass formation (vitrification) does not occur even at low temperatures Highly stressed agglomerates with interfacial cracks do not form Low temperature decomposition does not occur Voids evolve quickly and uniformly without vacuum Highly efficient chemical reactions proceed at low temperatures Microwaves penetrate uniformly through large volumes (m3) Microwaves do not heat glass, ceramics, or metals* Selective heating can be used for custom processing sequences Variable Frequency Microwaves are uniform and do not cause metal arcing * except at skin depth