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Related Concept Videos

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.
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Unlike ionic or small covalent molecules, polymers do not form crystalline solids due to the diffusion limitations of their long-chain structures. However, polymers contain microscopic crystalline domains separated by amorphous domains.
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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.
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Cationic Chain-Growth Polymerization: Mechanism00:57

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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 generated carbocation,...
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Some solids can transition directly into the gaseous state, bypassing the liquid state, via a process known as sublimation. At room temperature and standard pressure, a piece of dry ice (solid CO2) sublimes, appearing to gradually disappear without ever forming any liquid. Snow and ice sublimate at temperatures below the melting point of water, a slow process that may be accelerated by winds and the reduced atmospheric pressures at high altitudes. When solid iodine is warmed, the solid sublimes...
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The word polymer is derived from the Greek words “poly” which means “many” and “mer” which means “parts”. Polymers are long chains of molecules composed of repeating units of smaller molecules, known as monomers. They either occur naturally, such as DNA and proteins, or can be constructed synthetically, like plastics. They have varied structural characteristics, such as linear chains, branched chains, or complex networks, that contribute to the properties that they exhibit. Additionally,...

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Depolymerizable Olefinic Polymers Based on Fused-Ring Cyclooctene Monomers
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Polymer desorption under pulling: a dichotomic phase transition.

S Bhattacharya1, V G Rostiashvili, A Milchev

  • 1Max Planck Institute for Polymer Research, 10 Ackermannweg, 55128 Mainz, Germany.

Physical Review. E, Statistical, Nonlinear, and Soft Matter Physics
|April 28, 2009
PubMed
Summary
This summary is machine-generated.

This study reveals that pulling a polymer chain off an adhesive surface causes a first-order detachment transition, unlike the second-order transition without pulling. The critical adsorption exponent depends on loop interactions.

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Area of Science:

  • Polymer Physics
  • Surface Science
  • Statistical Mechanics

Background:

  • Understanding polymer behavior on surfaces is crucial for materials science and nanotechnology.
  • Adsorbed polymers exhibit complex structural properties and phase transitions.

Purpose of the Study:

  • To investigate the structural properties and phase behavior of a self-avoiding polymer chain on an adhesive substrate under pulling force.
  • To derive analytical expressions for structural units (loops, trains, tails) and determine the order of the detachment transition.

Main Methods:

  • Grand canonical ensemble approach for theoretical modeling.
  • Derivation of analytical expressions for probability distributions.
  • Extensive Monte Carlo simulations for verification.

Main Results:

  • Analytical expressions for loops, trains, and tails derived in terms of adhesive potential and pulling force.
  • Chain detachment transition under pulling is first-order, not second-order.
  • Critical adsorption exponent (φ) ranges from 0.34 to 0.59, dependent on loop interactions.

Conclusions:

  • The pulling force fundamentally alters the polymer adsorption-desorption transition dynamics.
  • Theoretical predictions align with simulation results, validating the model.
  • The study provides new insights into polymer-surface interactions under external forces.