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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...
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...
Polymers02:34

Polymers

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,...
Polymer Classification: Crystallinity01:21

Polymer Classification: Crystallinity

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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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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Structural Evolution during geopolymerization from an early age to consolidated material.

Prune Steins1, Arnaud Poulesquen, Olivier Diat

  • 1CEA, DEN, DTCD/SPDE/LP2C-Marcoule, F-30207 Bagnols sur Cèze, France.

Langmuir : the ACS Journal of Surfaces and Colloids
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Summary
This summary is machine-generated.

The polymerization of geopolymers is a stepwise process influenced by alkali activator size. Smaller cations like Na+ lead to distinct steps, while larger cations smooth the reaction, impacting gelation and water behavior.

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Area of Science:

  • Materials Science
  • Polymer Chemistry
  • Inorganic Synthesis

Background:

  • Geopolymers are inorganic polymers synthesized via alkaline activation of aluminosilicate sources.
  • Understanding geopolymerization mechanisms is crucial for developing advanced materials.
  • The role of alkali activators and water in geopolymer formation requires detailed investigation.

Purpose of the Study:

  • To investigate the time-resolved polymerization of geopolymers using multiple techniques.
  • To elucidate the influence of alkali activator cation size (Na+, K+, Cs+) on geopolymerization kinetics and structure.
  • To characterize the role of water molecules during the geopolymerization process.

Main Methods:

  • Time-resolved rheology to monitor viscoelastic moduli (G", G").
  • Small-angle X-ray scattering (SAXS) for nanoscale structural analysis.
  • Electron paramagnetic resonance (EPR) with spin probes to study water behavior.

Main Results:

  • Geopolymer curing proceeds in distinct steps, particularly with NaOH, linked to dissolution/polycondensation.
  • The size of alkali cations influences curing steps and gelation time, with smaller cations showing more pronounced effects.
  • SAXS reveals geopolymer growth via aggregation of sub-cation-sized oligomers.
  • EPR studies show water molecules are involved in early reactions and released upon gel formation, with hydration shell strength affecting signal visibility.

Conclusions:

  • Alkali cation size significantly impacts geopolymerization kinetics, structure, and water dynamics.
  • The observed stepwise curing and oligomer aggregation provide insights into geopolymer formation mechanisms.
  • Water plays a dynamic role throughout geopolymerization, influencing reaction pathways and final material properties.