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Related Concept Videos

Characteristics and Nomenclature of Copolymers01:24

Characteristics and Nomenclature of Copolymers

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...
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...
Cationic Chain-Growth Polymerization: Mechanism00:57

Cationic Chain-Growth Polymerization: Mechanism

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,...
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,...
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...
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...

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Synthesis of Monodisperse Cylindrical Nanoparticles via Crystallization-driven Self-assembly of Biodegradable Block Copolymers
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Fddd structure in AB-type diblock copolymers.

Kohtaro Yamada1, Makiko Nonomura, Takao Ohta

  • 1Yukawa Institute for Theoretical Physics, Kyoto University, Kyoto 606-8502, Japan.

Journal of Physics. Condensed Matter : an Institute of Physics Journal
|June 22, 2011
PubMed
Summary
This summary is machine-generated.

Researchers discovered a new equilibrium phase, the Fddd structure, in AB-type diblock copolymers. This interconnected, uniaxial phase expands the known equilibrium structures beyond lamellar, hexagonal, gyroid, and body-centered cubic phases.

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Area of Science:

  • Polymer Science
  • Materials Science
  • Soft Matter Physics

Background:

  • AB-type diblock copolymers exhibit well-established equilibrium structures like lamellar, hexagonal cylinder, gyroid, and body-centered cubic phases.
  • These structures arise from the self-assembly of polymer chains driven by unfavorable interactions between the blocks.

Purpose of the Study:

  • To identify and confirm the existence of novel equilibrium phases in AB-type diblock copolymers.
  • To characterize the structural and topological properties of newly discovered phases.

Main Methods:

  • Utilized a mode-expansion technique incorporating a significant number of modes to analyze phase behavior.
  • Performed direct three-dimensional simulations of the time-evolution equation to verify equilibrium structures.

Main Results:

  • Identified a previously unrecognized equilibrium phase, designated as the Fddd structure.
  • The Fddd structure is characterized as an interconnected but uniaxial network.
  • Confirmed the existence of the Fddd phase through two independent computational methods.

Conclusions:

  • The Fddd structure represents a fifth equilibrium phase in AB-type diblock copolymers.
  • This discovery expands the understanding of self-assembly phenomena in block copolymers.
  • The findings provide new insights into the complex phase diagrams of soft materials.