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Types of Step-Growth Polymers: Polyesters01:20

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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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Bioplastics derived from microbial processes present a sustainable alternative to conventional petroleum-based plastics. Among these, polyhydroxyalkanoates (PHAs), particularly polyhydroxybutyrates (PHBs), have emerged as prominent candidates due to their biodegradability and biocompatibility. These polymers are synthesized by a variety of bacteria, such as Cupriavidus necator and Pseudomonas putida, which naturally accumulate PHAs as intracellular carbon and energy reserves, especially under...
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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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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.
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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...
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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.
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Preparation of Biopolymer Aerogels Using Green Solvents
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Carbon dioxide as a polymer feedstock.

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Summary
This summary is machine-generated.

This review highlights 45 years of progress in using carbon dioxide (CO2) for polymer synthesis. Advanced catalysts enable efficient copolymerization of CO2 with epoxides and butadiene, creating valuable polycarbonates and other polymers.

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Area of Science:

  • Polymer Chemistry
  • Green Chemistry and Sustainability
  • Materials Science

Background:

  • The utilization of carbon dioxide (CO2) as a monomer in polymerization systems has been explored for over four decades.
  • Initial research focused on the copolymerization of CO2 with epoxides to produce polycarbonates, utilizing organozinc catalysts.
  • Catalyst development evolved to include zinc phenoxides and various metal-centered compounds, notably metal porphyrins.

Purpose of the Study:

  • To review the advancements in CO2 utilization for polymer synthesis over the past 45 years.
  • To discuss the evolution of catalysts and polymerization techniques for CO2-based polymers.
  • To highlight recent progress in copolymerizing CO2 with different monomers, such as butadiene.

Main Methods:

  • Review of seminal and subsequent research papers on CO2 polymerization.
  • Analysis of catalyst development, including organozinc compounds, zinc phenoxides, and metal porphyrins (Al, Co, Cr, Cu, Mn, lanthanides).
  • Examination of stereoregular polymer synthesis and recent methods involving lactone intermediates for CO2-butadiene copolymerization.

Main Results:

  • Successful synthesis of high molecular weight polycarbonates from CO2 and epoxides.
  • Development of diverse metal-centered catalysts, enhancing polymerization efficiency and control.
  • Emergence of advanced techniques like CO2-butadiene copolymerization via lactone intermediates using palladium catalysts.

Conclusions:

  • CO2 utilization in polymerization offers a sustainable pathway for waste valorization.
  • Significant progress has been made in catalyst design and polymerization strategies for CO2-based materials.
  • The synthesis of polycarbonates and other polymers from CO2 presents a promising route towards environmentally friendly chemical processes.