Stiffness Tuning and Ductility Enhancement of Semicrystalline Polymers by Incorporating Miscible Noncrystallizable Blocks

High Resolution Image Download MS PowerPoint Slide The mechanical behavior of hydrogenated poly(norbornene- b -substituted norbornene) diblock copolymers was investigated, where the substituted norbornene blocks are intimately mixed within the amorphous layer between hydrogenated polynorbornene (N) crystallites. In particular, hydrogenated poly(norbornene- b -norbornyl norbornene) diblock copolymers were studied; hydrogenated poly(norbornyl norbornene) homopolymers are glassy at room temperature. Enhancement of both yield stress and Young’s modulus was found at an enrichment of just 20 wt % glassy (G) block in the amorphous layer. Surprisingly, these N-G diblocks exhibit improved toughness over N homopolymers, with a nearly 4× decrease in minimum tie molecule fraction for ductility compared to quenched N homopolymers. Enhanced ductility is observed whether the substituted norbornene block is glassy or rubbery, as was demonstrated with a hydrogenated poly(norbornene- b -hexylnorbornene) diblock copolymer (N-R). These materials’ strain-hardening moduli reveal that the amorphous block promotes ductility by reducing disentanglement of tie molecules during drawing.

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Publication Details

Journal
ACS Macro Letters
Published
2026-07-23
DOI
https://doi.org/10.1021/acsmacrolett.6c00295
Primary Topic
Polymer crystallization and properties
Type
article
Field-Weighted Citation Impact
0.00

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article

Stiffness Tuning and Ductility Enhancement of Semicrystalline Polymers by Incorporating Miscible Noncrystallizable Blocks

Richard A. Register, Katherine M. Gunter
ACS Macro Letters
Polymer crystallization and properties
article

Stiffness Tuning and Ductility Enhancement of Semicrystalline Polymers by Incorporating Miscible Noncrystallizable Blocks

Richard A. Register, Katherine M. Gunter
article en

Abstract

High Resolution Image Download MS PowerPoint Slide The mechanical behavior of hydrogenated poly(norbornene- b -substituted norbornene) diblock copolymers was investigated, where the substituted norbornene blocks are intimately mixed within the amorphous layer between hydrogenated polynorbornene (N) crystallites. In particular, hydrogenated poly(norbornene- b -norbornyl norbornene) diblock copolymers were studied; hydrogenated poly(norbornyl norbornene) homopolymers are glassy at room temperature. Enhancement of both yield stress and Young’s modulus was found at an enrichment of just 20 wt % glassy (G) block in the amorphous layer. Surprisingly, these N-G diblocks exhibit improved toughness over N homopolymers, with a nearly 4× decrease in minimum tie molecule fraction for ductility compared to quenched N homopolymers. Enhanced ductility is observed whether the substituted norbornene block is glassy or rubbery, as was demonstrated with a hydrogenated poly(norbornene- b -hexylnorbornene) diblock copolymer (N-R). These materials’ strain-hardening moduli reveal that the amorphous block promotes ductility by reducing disentanglement of tie molecules during drawing.

ACS Macro Letters
Princeton University (US)
National Science Foundation, Division of Materials Research
Openalex Percentile: Top 18%
Polymer crystallization and properties
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