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This study details the enhancement of CO2 selectivity in ring opening metathesis polymerization (ROMP) polymers that contain nitrile moieties and micro-pore generating ladder side chains. A material, CN-ROMP homopolymer, with nitriles in the ladder side chains was originally targeted and synthesized, however its low molecular weight and backbone rigidity precluded film formation. As a result, an alternative method was pursued wherein copolymers were synthesized using norbornene (N) and nitrile norbornene (NN). Herein, we report an investigation of the structure–property relationships of backbone functionalization and grafting density on the CO2 transport properties in these ROMP polymers. Nitrile-containing copolymers showed an increase in CO2/CH4 sorption selectivity and a concomitant increase in CO2/CH4 permselectivity when compared to the unfunctionalized (nitrile free) analogs. The stability in CO2 rich environments is enhanced as grafting density of the rigid, pore-generating side chains increases and an apparent tunability of CO2 plasticization pressure was observed as a function of norbornene content. Lower loadings of norbornene resulted in higher plasticization pressure points. Gas permeability in the ROMP copolymers was found to correlate most strongly with the concentration of ladder macromonomers in the polymer chain.
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Exploring the influence of rigid carbocycles on terpenoid copolymer properties
Abstract Synthesizing soft polymers with uncommon architectural elements is critical for enhancing our understanding of fundamental structure–property relationships in macromolecules. Terpenoid materials are interesting candidates for addressing this grand challenge, as their constituent monomers can exhibit a diverse array of structural and functional groups. Moreover, these biologically‐derived materials can potentially expand the sphere of knowledge surrounding trends in related petrochemically‐derived polymers. For example, vinyl‐addition copolymers of norbornene and acyclic olefins can exhibit predictable properties (e.g., linear changes inTgas a function of composition). Due to synthetic limitations, however, it is not well understood if other rigid carbocycles engender similar behavior in a range of copolymers. As numerous terpene scaffolds display rigid motifs (such as pinane systems), terpenoid polymers are uniquely positioned to address this deficiency. Here, we report the synthesis and characterization of terpenoid copolymers (both statistical and block) with systematically tailored compositions of pinene‐based comonomers. We found that the pinane core (which is a constitutional isomer of norbornene) appears to promote ideal behavior with regard to bulk thermal properties of statistical copolymers, which mirrors the behavior of norbornene‐based systems. We also found that block copolymers exhibited thermomechanical properties that were highly tunable (and apparently correlated to carbocycle composition).
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- Award ID(s):
- 2206955
- PAR ID:
- 10413058
- Publisher / Repository:
- Wiley Blackwell (John Wiley & Sons)
- Date Published:
- Journal Name:
- Journal of Polymer Science
- Volume:
- 61
- Issue:
- 17
- ISSN:
- 2642-4150
- Page Range / eLocation ID:
- p. 1995-2001
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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