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Related Concept Videos

Fast Reactions01:27

Fast Reactions

Fast reactions occurring in times shorter than the time needed to mix reactants pose a unique challenge for investigation. In a liquid-phase continuous-flow system, reactants A and B are swiftly pushed into the mixing chamber, where mixing occurs within 1 ms. The reaction mixture then flows through an observation tube, and one measures light absorption to determine species concentrations at various points of the tube. This method is most appropriate when relatively large volumes of reactants...
Free-Radical Chain Reaction and Polymerization of Alkenes02:35

Free-Radical Chain Reaction and Polymerization of Alkenes

The conversion of alkenes to macromolecules called polymers is a reaction of high commercial importance. The structure of the polymer is defined by a repeating unit, while the terminal groups are considered insignificant. The average degree of polymerization represents the number of repeating units in the polymer molecule and is denoted by the subscript n.
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...
Olefin Metathesis Polymerization: Overview01:13

Olefin Metathesis Polymerization: Overview

Recently, the development of olefin metathesis polymerization advanced the field of polymer synthesis. Simply put, the reorganization of substituents on their double bonds between two olefins in the presence of a catalyst is known as the olefin metathesis reaction. The use of metathesis reaction for polymer synthesis is called olefin metathesis polymerization.
Ruthenium-based Grubbs catalyst is the most commonly used catalyst for olefin metathesis polymerization. Grubbs catalyst consists of a...
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,...
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...

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Ethylene Polymerizations Using Parallel Pressure Reactors and a Kinetic Analysis of Chain Transfer Polymerization
07:28

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Published on: November 27, 2015

Continuous flow enzyme-catalyzed polymerization in a microreactor.

Santanu Kundu1, Atul S Bhangale, William E Wallace

  • 1Polymers Division, National Institute of Standards and Technology, Gaithersburg, Maryland 20899, United States.

Journal of the American Chemical Society
|March 29, 2011
PubMed
Summary
This summary is machine-generated.

Enzyme-catalyzed polymerization using microreactors offers a greener, continuous process. This novel approach achieves faster reactions and higher molecular mass polycaprolactone compared to traditional batch methods.

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Area of Science:

  • Biocatalysis and Polymer Chemistry
  • Chemical Engineering and Process Intensification

Background:

  • Enzymes immobilized on solid supports enable sustainable chemical transformations.
  • Microreactors offer advantages for controlling heterogeneous reactions.

Purpose of the Study:

  • To investigate enzyme-catalyzed ring-opening polymerization of ε-caprolactone using a novel microreactor design.
  • To compare the performance of microreactors with batch reactors for this polymerization process.

Main Methods:

  • Utilized a novel microreactor for continuous flow, enzyme-catalyzed ring-opening polymerization of ε-caprolactone.
  • Employed solid-supported enzymes in organic media at elevated temperatures.
  • Compared polymerization kinetics and product properties with conventional batch reactors.

Main Results:

  • Achieved faster polymerization rates in the microreactor system.
  • Produced polycaprolactone with higher molecular mass compared to batch processes.
  • Demonstrated the feasibility of continuous flow for solid-supported enzyme-catalyzed polymerization.

Conclusions:

  • Microreactor technology enables efficient and sustainable enzyme-catalyzed polymerization.
  • This platform can be adapted for high-throughput screening and precision measurements in biocatalysis.
  • Represents the first continuous flow demonstration of solid-supported enzyme-catalyzed polymerization.