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The introduction of polyesters has brought major development to the textile industry. The wrinkle-free behavior of polyester blends has eliminated the need for starching and ironing clothes.
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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.
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Polymerization generates chiral centers along the entire backbone of a polymer chain. Accordingly, the stereochemistry of the substituent group has a significant effect on polymer properties. Polymers formed from monosubstituted alkene monomers feature chiral carbons at every alternate position in the polymer backbone. Relative to the predominant orientation of substituents at the adjacent chiral carbons, the polymer can exist in three different configurations: isotactic, syndiotactic, and...
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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 Homopolymers01:00

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Polymers that are made up of identical monomer units are called homopolymers. Only one repeating unit is involved in the construction of the homopolymer structure. For example, as depicted in Figure 1, polypropylene is a homopolymer constituted of propylene monomers. Here, the only repeating unit in the polymer chain is propylene.
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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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Chemically Recyclable Ester-Linked Polypropylene.

Andrew L Kocen1, Shilin Cui1, Ting-Wei Lin1

  • 1Department of Chemistry and Chemical Biology, Baker Laboratory, Cornell University, Ithaca, New York 14853-1301, United States.

Journal of the American Chemical Society
|July 6, 2022
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Summary
This summary is machine-generated.

This study introduces a new catalyst for propylene and butadiene copolymerization, enabling chemical recycling of polyolefins. The process creates recyclable ester-linked polypropylene with properties similar to conventional polyolefins.

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Area of Science:

  • Polymer Chemistry
  • Materials Science
  • Sustainable Chemistry

Background:

  • Polyolefins are widely used commodity materials with excellent properties but limited recyclability.
  • Current recycling methods for polyolefins are insufficient, leading to significant waste.
  • Developing chemical recycling pathways for polyolefins is crucial for sustainability.

Purpose of the Study:

  • To develop a novel catalyst for isoselective copolymerization of propylene and butadiene.
  • To establish a chemical recycling process for producing ester-linked polypropylene.
  • To demonstrate the recyclability of the newly synthesized ester-linked polypropylene.

Main Methods:

  • Isoselective copolymerization of propylene and butadiene using a new catalyst.
  • Depolymerization of the unsaturated copolymer to a telechelic macromonomer via olefin metathesis.
  • Hydrogenation of the macromonomer and subsequent repolymerization to form ester-linked polypropylene.

Main Results:

  • A new catalyst demonstrated high selectivity for 1,4-insertion of butadiene in propylene copolymerization.
  • The process yielded telechelic macromonomers and ester-linked polypropylene with properties comparable to linear low-density polyethylene.
  • The ester-linked polypropylene could be depolymerized back to the telechelic macromonomer, enabling chemical recycling.

Conclusions:

  • A viable chemical recycling route for polyolefins has been established through a novel catalytic process.
  • The developed method transforms unsaturated polyolefins into recyclable materials with desirable properties.
  • This approach offers a sustainable alternative for managing polyolefin waste.