Dispersive Component of Surface Energy

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SUMMARY

The discussion centers on the dispersive component of surface energy in plastic polymers treated with a micro atmospheric pressure plasma jet (μ-APPJ) using helium (He) as the carrier gas and varying oxygen (O2) admixtures of 1/2%, 1%, and 2%. The user seeks clarification on the definition of the dispersive component and its apparent stability despite changes in treatment conditions. It is established that the dispersive component relates to van der Waals forces and typically remains constant across different heating and polar component scenarios, indicating a fundamental property of the material's surface.

PREREQUISITES
  • Understanding of surface energy concepts
  • Familiarity with plasma treatment processes, specifically μ-APPJ
  • Knowledge of van der Waals forces
  • Basic principles of polymer chemistry
NEXT STEPS
  • Research the definition and significance of the dispersive component of surface energy
  • Explore the effects of μ-APPJ treatment on various plastic polymers
  • Investigate the relationship between surface energy and plasma treatment parameters
  • Learn about surface energy measurement techniques for polymers
USEFUL FOR

Researchers and students in materials science, polymer chemistry, and surface engineering, particularly those focusing on plasma treatment effects on polymer surfaces.

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Hello, I'm doing an MSc project concerned with the treatment of plastic polymers with an μ-APPJ. I have been getting a tonne of results on different plastics using an APPJ of He carrier gas with an Oxygen admixture of 1/2, 1 & 2%.

However, in my analysis I'm unsure of what the dispersive component of the surface energy is and why it more or less stays the same.

Can someone give me a definition of what it is? I think its to do with van der waals but nothing on the net is giving me a good answer.

Is it supposed to stay the same irrespective of whether the material has been heated up or its polar component increases?

How would I interpret my data on the surface energies for example:

He_o2_SurfaceEnergy_zpsdf773115.png


For convention, -5mins to 0mins is the 5minutes of plasma treatment. I'm not measuring the plastic during this time, hence the constant values and the discontinuity when I first measure it after treatment.
This is one of my preliminary results with Acetate plastic. Treated 1 run with He gas, 2nd run with He + O2. The legend will tell you. The dispersive components stay relatively the same, why?
 
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Can anyone tell me what the definition of Dispersive Component is?
 
Bump, I still don't know what constitutes the Dispersive Component of Surface Energy.
 

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