Bridging polymer architecture, printability, and properties by digital light processing of block copolycarbonates
Krista G Schoonover1, Chia-Min Hsieh1, Mani Sengoden1
1Department of Chemistry, Texas A&M University 3255 TAMU College Station TX 77843 USA djdarens@chem.tamu.edu emilypentzer@tamu.edu.
Tailoring monomer ratio and polymer architecture in carbon dioxide-based aliphatic polycarbonates (aPCs) is key for digital light processing (DLP) additive manufacturing. This approach optimizes mechanical properties and degradation rates for sustainable materials.
Area of Science:
- Polymer Chemistry
- Materials Science
- Sustainable Manufacturing
Background:
- Carbon dioxide-based aliphatic polycarbonates (aPCs) offer renewable feedstock and degradability.
- Modifying aPCs' mechanical properties remains a challenge for specific applications.
Purpose of the Study:
- To investigate how monomer ratio and polymer architecture affect the printability and properties of aPCs.
- To explore the potential of aPCs in digital light processing (DLP) additive manufacturing.
Main Methods:
- Alternating copolymerization of epoxides with CO2 to produce aPCs.
- Digital Light Processing (DLP) additive manufacturing of aPCs with varying compositions and architectures.
- Thermomechanical property testing and hydrolytic degradation studies.
Main Results:
- Block copolymers (BCPs) showed tunable thermomechanical properties based on hard block content, ranging from elastomeric to brittle.
- Homopolymer blends failed to print, while statistical copolymers exhibited poor mechanical properties and delamination.
- BCP prints with higher hard block content degraded slower; statistical copolymers degraded slower than BCPs.
Conclusions:
- Monomer ratio and polymer architecture are critical for aPC resin printability and bulk properties.
- Polymer design offers significant potential for advancing sustainable materials in additive manufacturing.
- Tailored aPCs can be successfully fabricated into functional objects via DLP.
More Related Videos
11:42Synthesis of Monodisperse Cylindrical Nanoparticles via Crystallization-driven Self-assembly of Biodegradable Block Copolymers
Published on: June 20, 2019
10:09Fabricating Reactive Surfaces with Brush-like and Crosslinked Films of Azlactone-Functionalized Block Co-Polymers
Published on: June 30, 2018
Related Concept Videos
Types of Step-Growth Polymers: Polyesters
Polyesters are commonly prepared from terephthalic acid and ethylene glycol; the crude product is known as poly(ethylene terephthalate) or PET. However, polyesters are synthesized industrially by transesterification of dimethyl terephthalate with ethylene glycol at 150 °C. The two reactants and the...
Characteristics and Nomenclature of Copolymers
Polymer Classification: Architecture
Polymer Classification: Crystallinity
Crystalline domains are the regions where polymer chains are aligned in an orderly manner and held together in proximity by intermolecular forces. For example, chains in the crystalline domains of polyethylene and nylon are bound together by van der Waals...
Anionic Chain-Growth Polymerization: Overview
Cationic Chain-Growth Polymerization: Mechanism
