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Related Concept Videos

Cationic Chain-Growth Polymerization: Mechanism00:57

Cationic Chain-Growth Polymerization: Mechanism

2.5K
The cationic polymerization mechanism consists of three steps: initiation, propagation, and termination. In the initiation step of the polymerization process, the π bond of a monomer gets protonated by the Lewis acid catalyst, which is formed from boron trifluoride and water. The protonation of the π bond generates a carbocation stabilized by the electron‐donating group. In the propagation step, the π bond of the second monomer acts as a nucleophile and attacks the...
2.5K
Step-Growth Polymerization: Overview01:03

Step-Growth Polymerization: Overview

3.9K
Step-growth or condensation polymerization is a stepwise reaction of bi or multifunctional monomers to form long-chain polymers. As all the monomers are reactive, most of the monomers are consumed at the early stages of the reaction to form small chains of reactive oligomers, which then combine to form long polymer chains in the late stages. Hence, the reaction has to proceed for a long time to achieve high molecular weight polymers.
Many natural and synthetic polymers are produced by...
3.9K
Anionic Chain-Growth Polymerization: Mechanism01:04

Anionic Chain-Growth Polymerization: Mechanism

2.2K
The mechanism for anionic chain-growth polymerization involves initiation, propagation, and termination steps. In the initiation step, a nucleophilic anion, such as butyl lithium, initiates the polymerization process by attacking the π bond of the vinylic monomer. As a result, a carbanion, stabilized by the electron‐withdrawing group, is generated. The resulting carbanion acts as a Michael donor in the propagation step and attacks the second vinylic monomer, which acts as a Michael...
2.2K
Anionic Chain-Growth Polymerization: Overview01:20

Anionic Chain-Growth Polymerization: Overview

2.3K
The polymerization process that involves carbanion as an intermediate is called anionic polymerization. It is also a type of addition or chain-growth polymerization. Anionic polymerization gets initiated by a strong nucleophile such as an organolithium or a Grignard reagent. The most commonly used initiator for anionic polymerization is butyl lithium. Monomers involved in anionic polymerization must possess a vinyl group bonded to one or two electron-withdrawing groups. For instance,...
2.3K
Molecular Weight of Step-Growth Polymers01:08

Molecular Weight of Step-Growth Polymers

2.6K
Step growth polymerization involves bi or multifunctional monomers. Bifunctional monomers react to form linear step growth polymers, whereas multifunctional monomers react to form non-linear or branched polymers.
As the step-growth polymerization involves step-wise condensation of monomers, the molecular weight also builds up eventually. Consequently, high molecular weight polymers are obtained at the late stages of the polymerization, where 99% of monomers have been consumed.
The extent of the...
2.6K

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Fabricating Reactive Surfaces with Brush-like and Crosslinked Films of Azlactone-Functionalized Block Co-Polymers
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Achieving Stable Patterns in Multicomponent Polymer Thin Films Using Marangoni and van der Waals Forces.

Saurabh Shenvi Usgaonkar1, Christopher J Ellison1, Satish Kumar1

  • 1Department of Chemical Engineering and Materials Science, University of Minnesota, Minneapolis, Minnesota 55455, United States.

Langmuir : the ACS Journal of Surfaces and Colloids
|May 28, 2021
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Summary
This summary is machine-generated.

Surface tension gradients deform liquid-air interfaces for polymer film patterning. Blending polymers delays topography decay, offering enhanced control in photochemical patterning applications.

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Area of Science:

  • Surface science
  • Polymer physics
  • Fluid dynamics

Background:

  • Liquid-air interfaces can be patterned using surface-tension gradients.
  • Photochemical patterning of solid polymer films induces these gradients.
  • Topography decay is a limitation due to capillary leveling and diffusion.

Purpose of the Study:

  • Investigate methods to enhance the stability of topographical features in patterned polymer films.
  • Understand the role of polymer blends in delaying topography dissipation.
  • Develop a theoretical model to explain experimental observations.

Main Methods:

  • Developed a lubrication theory model.
  • Derived coupled nonlinear partial differential equations for film height and species concentration.
  • Incorporated nonmonotonic disjoining pressure into the model.

Main Results:

  • Model predictions show qualitative agreement with experimental observations.
  • Nonmonotonic disjoining pressure significantly increases the lifetime of topographical features.
  • Parametric study identified key variables controlling deformation kinetics.

Conclusions:

  • Polymer blends can significantly delay topography decay in patterned films.
  • The developed model provides insights into the mechanisms governing topography stability.
  • Findings offer guidelines for optimizing photochemically induced Marangoni patterning.