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Related Concept Videos

Radical Chain-Growth Polymerization: Chain Branching01:17

Radical Chain-Growth Polymerization: Chain Branching

The skeletal structure of polymers synthesized via radical polymerization is always branched. For example, the polymerization of ethylene by radical polymerization results in a low-density grade of polyethylene with a heavily branched skeletal structure. Here, the radical site abstracts hydrogen from the growing chain, and the radical site shifts from the end (a primary carbon center) to anywhere within the growing chain (a secondary carbon center). Consequently, the part of the chain from the...
Ziegler–Natta Chain-Growth Polymerization: Overview01:17

Ziegler–Natta Chain-Growth Polymerization: Overview

Ziegler–Natta polymerization is another form of addition or chain‐growth polymerization used for synthesizing linear polymers over branched polymers. The catalyst used for polymerization is the Ziegler–Natta catalyst, named after Karl Ziegler and Giulio Natta, who developed it in 1953. This catalyst is an organometallic complex of titanium tetrachloride and triethyl aluminum, with the active form of the catalyst being an alkyl titanium compound. Using the Ziegler–Natta catalyst, high molecular...
Generation of Straight or Branched Actin Filaments01:14

Generation of Straight or Branched Actin Filaments

The straight or branched structure formation of actin filaments is controlled by nucleating proteins such as the formins and Arp2/3 complex. Formin-mediated assembly results in straight filaments, whereas Arp2/3 protein complex-mediated assembly results in branched actin filaments.
Arp2/3 Complex
Arp2/3 complex is a seven-subunit complex consisting of two proteins similar to actin- Arp2 and Arp3, and five other subunits that help keep Arp2 and Arp3 inactive. When required, the complex is...
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.
Radical Chain-Growth Polymerization: Overview01:10

Radical Chain-Growth Polymerization: Overview

Chain-growth or addition polymerization is successive addition reactions of monomers with a polymer chain. In radical chain-growth polymerization, the reaction proceeds via a free-radical intermediate. The free radical is formed from radical initiators, which spontaneously generate free radicals by homolytic fission. Organic peroxides (such as dibenzoyl peroxide, as shown in Figure 1) or azo compounds are popular radical initiators. A low concentration ratio of radical initiator to monomer is...
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,...

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Facet-to-facet Linking of Shape-anisotropic Colloidal Cadmium Chalcogenide Nanostructures
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Decorated, tapered, and highly nonlinear granular chain.

Robert Doney1, Surajit Sen

  • 1U.S. Army Research Laboratory, Aberdeen Proving Grounds, Maryland 21005, USA.

Physical Review Letters
|December 13, 2006
PubMed
Summary

Tapered granular chains offer excellent energy absorption, improving with size and tapering. A new solution enhances performance for all chain sizes, showcasing impressive shock mitigation capabilities.

Area of Science:

  • Physics
  • Materials Science
  • Mechanical Engineering

Background:

  • Inertial mismatches in 1D granular chains enhance energy absorption.
  • Performance scales with the number of spheres (N) and tapering (q).
  • Short chains have limited energy absorption capacity.

Purpose of the Study:

  • To present a solution for improving energy absorption in granular chains of any size.
  • To analyze the nonlinear dynamics and shock absorption characteristics.
  • To illustrate mitigation capabilities using normalized kinetic energy diagrams.

Main Methods:

  • Investigated 1D granular chains with inertial mismatches.
  • Developed and analyzed an improved tapered chain design.
  • Utilized normalized kinetic energy diagrams to assess performance.

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Facet-to-facet Linking of Shape-anisotropic Colloidal Cadmium Chalcogenide Nanostructures
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Scalable Nanohelices for Predictive Studies and Enhanced 3D Visualization

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Main Results:

  • The proposed solution significantly enhances energy absorption for all chain sizes.
  • Granular chain dynamics are complex and not accurately modeled by hard-sphere approximations.
  • Shock absorption capacity varies with position along the chain.

Conclusions:

  • The improved tapered granular chains demonstrate superior energy absorption and shock mitigation.
  • These nonlinear, scalable systems offer a promising solution for impact protection.
  • Further research into their complex dynamics is warranted.