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Related Concept Videos

Step-Growth Polymerization: Overview01:03

Step-Growth Polymerization: Overview

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...
Molecular Weight of Step-Growth Polymers01:08

Molecular Weight of Step-Growth Polymers

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...
Types of Step-Growth Polymers: Polyesters01:20

Types of Step-Growth Polymers: Polyesters

The introduction of polyesters has brought major development to the textile industry. The wrinkle-free behavior of polyester blends has eliminated the need for starching and ironing clothes.
Polyesters are commonly prepared from terephthalic acid and ethylene glycol; the crude product is known as poly(ethylene terephthalate) or PET. However, polyesters are synthesized industrially by transesterification of dimethyl terephthalate with ethylene glycol at 150 °C. The two reactants and the polymer...
Polymer Classification: Architecture01:14

Polymer Classification: Architecture

Polymers are classified as linear or branched on the basis of their chain architecture. The polymer chains in linear polymers have a long chain-like structure with minimal to no branching at all. Even if a polymer features large substituent groups on the monomer, which appear as branches to the skeleton, it is not considered a branched polymer. A branched polymer contains secondary polymer chains that arise from the main polymer chain. The branching occurs when the polymer growth shifts from...
Anionic Chain-Growth Polymerization: Overview01:20

Anionic Chain-Growth Polymerization: Overview

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,...
Anionic Chain-Growth Polymerization: Mechanism01:04

Anionic Chain-Growth Polymerization: Mechanism

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 acceptor.

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Related Experiment Video

Updated: May 9, 2026

Preparation and Friction Force Microscopy Measurements of Immiscible, Opposing Polymer Brushes
13:57

Preparation and Friction Force Microscopy Measurements of Immiscible, Opposing Polymer Brushes

Published on: December 24, 2014

Size-dependent transitions in grafted polymer brushes.

Marian Manciu1, Courtney Bosse, Eli Ruckenstein

  • 1Physics Department, University of Texas at El Paso, El Paso, Texas 79968, USA. mmanciu@utep.edu

The Journal of Physical Chemistry. B
|July 25, 2013
PubMed
Summary
This summary is machine-generated.

Infinite polymer chains with segment-surface interactions either collapse or stretch. Finite chains exhibit transitions between collapsed "trains" and stretched "tails" based on interaction strength and chain length.

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Particles without a Box: Brush-first Synthesis of Photodegradable PEG Star Polymers under Ambient Conditions
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Particles without a Box: Brush-first Synthesis of Photodegradable PEG Star Polymers under Ambient Conditions

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Last Updated: May 9, 2026

Preparation and Friction Force Microscopy Measurements of Immiscible, Opposing Polymer Brushes
13:57

Preparation and Friction Force Microscopy Measurements of Immiscible, Opposing Polymer Brushes

Published on: December 24, 2014

Density Gradient Multilayered Polymerization (DGMP): A Novel Technique for Creating Multi-compartment, Customizable Scaffolds for Tissue Engineering
12:54

Density Gradient Multilayered Polymerization (DGMP): A Novel Technique for Creating Multi-compartment, Customizable Scaffolds for Tissue Engineering

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Particles without a Box: Brush-first Synthesis of Photodegradable PEG Star Polymers under Ambient Conditions
06:56

Particles without a Box: Brush-first Synthesis of Photodegradable PEG Star Polymers under Ambient Conditions

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Area of Science:

  • Polymer Physics
  • Surface Science
  • Statistical Mechanics

Background:

  • Grafted polymer brushes are crucial in various applications, from coatings to biomaterials.
  • Understanding their conformational behavior under different interactions is key to controlling their properties.

Purpose of the Study:

  • To theoretically investigate the conformational states of grafted polymer brushes.
  • To determine the conditions leading to collapsed or stretched configurations.

Main Methods:

  • Calculation of the partition function for a grafted polymer brush.
  • Derivation of a system of equations for the most likely configuration.
  • Analysis of solutions for both infinite and finite polymer chains.

Main Results:

  • Infinite chains with non-vanishing segment-surface interactions do not have a stable intermediate configuration.
  • Finite chains exhibit a transition from loops to trains (collapse) with attractive interactions.
  • Finite chains show a transition from loops to tails (stretching) with repulsive interactions.

Conclusions:

  • The behavior of grafted polymer brushes is highly dependent on segment-surface interactions.
  • Transitions to collapsed or stretched states are influenced by chain length, segment-segment interactions, segment-solvent interactions, and grafting density.