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Polymers: Molecular Weight Distribution01:10

Polymers: Molecular Weight Distribution

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For any given polymer, the weight average molecular weight (Mw) is higher than, if not equal to, the number average molecular weight (Mn). The only situation in which the weight average molecular weight and the number average molecular weight are equal is when a polymer consists only of chains with equal molecular weight. However, this never happens in a synthetic polymer, since it is difficult to control the polymerization process up to a molecular level with accuracy to a hundred percent.
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Molecular Weight of Step-Growth Polymers01:08

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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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Olefin Metathesis Polymerization: Ring-Opening Metathesis Polymerization (ROMP)01:16

Olefin Metathesis Polymerization: Ring-Opening Metathesis Polymerization (ROMP)

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Ring-opening metathesis polymerization or ROMP involves strained cycloalkenes as starting materials. The mechanism of ROMP proceeds by reacting cycloalkene with Grubbs catalyst to give metallacyclobutane intermediate which undergoes a ring-opening reaction to form new carbene. The new carbene reacts with another molecule of cycloalkene. Repetition of these steps leads to the formation of an unsaturated open-chain polymer product. All these steps are reversible, however, relieving the ring...
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Polymers: Defining Molecular Weight01:01

Polymers: Defining Molecular Weight

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Unlike small molecules with definite molecular weights, polymers are a mixture of individual polymer chains of varying lengths, each with a unique molecular weight.  So, the molecular weight of a polymer is expressed as an average value based on the average size of the polymer chains. The two most common forms of averages used for polymers are the number average molecular weight and weight average molecular weight.
The number average molecular weight (Mn) is the summation of the number...
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Polymer Classification: Architecture01:14

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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...
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Characteristics and Nomenclature of Copolymers01:24

Characteristics and Nomenclature of Copolymers

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Copolymers are the products obtained from the polymerization of multiple monomer species. So, in a polymer chain itself, there can be multiple repeating units that come from different monomers. The process of synthesizing a polymer from different monomer species is called copolymerization. When two monomers are involved, the polymer is known as a bipolymer. Polymers with three and four monomers are termed terpolymers and quaterpolymers, respectively. Figure 1 depicts the copolymerization of...
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Size distribution of ring polymers.

Shlomi Medalion1,2, Erez Aghion1,2, Hagai Meirovitch1

  • 1Department of Physics, Bar-Ilan University, Ramat-Gan, 52900, Israel.

Scientific Reports
|June 16, 2016
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Summary
This summary is machine-generated.

We solved the average distance distribution for ring polymers. This reveals universal behaviors across dimensions, linking polymer physics to Bessel process distributions.

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Area of Science:

  • Polymer Physics
  • Statistical Mechanics
  • Stochastic Processes

Background:

  • Understanding the spatial distribution of polymer chains is crucial in polymer physics.
  • Previous studies have explored monomer distances in linear and branched polymers, but ring polymers present unique topological challenges.
  • The connection between polymer conformations and random walk distributions is a well-established concept.

Purpose of the Study:

  • To derive an exact solution for the distribution of sample-averaged monomer-to-monomer distances in ring polymers.
  • To explore the relationship between these distributions and known stochastic processes like Bessel bridges and excursions.
  • To investigate the dimensional dependence and universality of these polymer properties.

Main Methods:

  • Analytical solution derivation for non-interacting and local-interaction ring polymer models.
  • Mapping polymer distance distributions to area distributions of reflected Bessel bridges and Bessel excursions.
  • Numerical analysis for self-avoiding polymers in various dimensions.

Main Results:

  • Identical distributions for non-interacting and local-interaction models in dimensions d ≥ 2, with finite size effects at d=2.
  • A d ↔ 4-d symmetry was discovered, showing the Airy distribution for 1D Brownian excursions also describes 3D ring polymers.
  • Scaled averaged distance fluctuations for self-avoiding polymers in d=2, 3 are nearly identical and approximated by the 5D non-interacting model.

Conclusions:

  • The study provides an exact solution for ring polymer distances, revealing universal scaling laws.
  • The findings establish a direct link between polymer physics and the mathematical framework of Bessel processes.
  • The discovered dimensional symmetry offers new insights into polymer behavior across different spatial dimensions.