Polymer crystal nucleation with confinement-enhanced orientation dominating the formation of nanohybrid shish-kebabs with multiple shish

RSC Advances ◽  
2016 ◽  
Vol 6 (56) ◽  
pp. 50451-50459 ◽  
Author(s):  
Yijing Nie ◽  
Tongfan Hao ◽  
Ya Wei ◽  
Zhiping Zhou

An unexpected NHSK structure with multiple shish is observed. The aligned fillers act as multiple shish and the polymer crystal lamellae form kebabs.

Polymers ◽  
2020 ◽  
Vol 12 (2) ◽  
pp. 447 ◽  
Author(s):  
Kyle Wm. Hall ◽  
Timothy W. Sirk ◽  
Simona Percec ◽  
Michael L. Klein ◽  
Wataru Shinoda

This study demonstrates that monodisperse entangled polymer melts crystallize via the formation of nanoscale nascent polymer crystals (i.e., nuclei) that exhibit substantial variability in terms of their constituent crystalline polymer chain segments (stems). More specifically, large-scale coarse-grain molecular simulations are used to quantify the evolution of stem length distributions and their properties during the formation of polymer nuclei in supercooled prototypical polyethylene melts. Stems can adopt a range of lengths within an individual nucleus (e.g., ∼1–10 nm) while two nuclei of comparable size can have markedly different stem distributions. As such, the attainment of chemically monodisperse polymer specimens is not sufficient to achieve physical uniformity and consistency. Furthermore, stem length distributions and their evolution indicate that polymer crystal nucleation (i.e., the initial emergence of a nascent crystal) is phenomenologically distinct from crystal growth. These results highlight that the tailoring of polymeric materials requires strategies for controlling polymer crystal nucleation and growth at the nanoscale.


2018 ◽  
Author(s):  
Kyle Hall ◽  
Simona Percec ◽  
Michael Klein

<p>This study reveals two important features of polymer crystal formation at high-driving forces in entangled polymer melts based on molecular dynamics simulations of polyethylene, a prototypical polymer. First, in contrast to existing literature on small-molecule crystallization, it is demonstrated that the heat released during polymer crystallization does not appreciably influence molecular-level structural details of early-stage, crystalline clusters (i.e., polymer crystal nuclei). Second, it is revealed that early-stage polymer crystallization (i.e., crystal nucleation) can occur without substantial chain-level relaxation and conformational changes, which is consistent with previous experimental work and yet in contrast to many previous computational studies. Given the conditions used to process polyethylene, the separation of timescales associated with crystallization and chain-level processes is anticipated to be of substantial importance to processing strategies. This study thus provides insights that highlight new research directions for understanding polymer crystallization under industrially-relevant conditions while also providing guidance as to how this work can be undertaken.</p>


2020 ◽  
Vol 124 (23) ◽  
pp. 4793-4804
Author(s):  
Kyle Wm. Hall ◽  
Simona Percec ◽  
Wataru Shinoda ◽  
Michael L. Klein

2006 ◽  
Vol 97 (24) ◽  
Author(s):  
Michael V. Massa ◽  
Jessica L. Carvalho ◽  
Kari Dalnoki-Veress

2021 ◽  
Vol 54 (4) ◽  
pp. 1599-1610
Author(s):  
Kyle Wm. Hall ◽  
Simona Percec ◽  
Wataru Shinoda ◽  
Michael L. Klein

Author(s):  
E. L. Thomas ◽  
S. L. Sass

In polyethylene single crystals pairs of black and white lines spaced 700-3,000Å apart, parallel to the [100] and [010] directions, have been identified as microsector boundaries. A microsector is formed when the plane of chain folding changes over a small distance within a polymer crystal. In order for the different types of folds to accommodate at the boundary between the 2 fold domains, a staggering along the chain direction and a rotation of the chains in the plane of the boundary occurs. The black-white contrast from a microsector boundary can be explained in terms of these chain rotations. We demonstrate that microsectors can terminate within the crystal and interpret the observed terminal strain contrast in terms of a screw dislocation dipole model.


RSC Advances ◽  
2021 ◽  
Vol 11 (26) ◽  
pp. 15710-15721
Author(s):  
Paavai Era ◽  
RO. MU. Jauhar ◽  
V. Viswanathan ◽  
M. Madhangi ◽  
G. Vinitha ◽  
...  

This paper discusses the structural orientations and the physico-chemical properties of a single crystal of 2-amino-4,6-dimethoxypyrimidinium hydrogen (2R,3R)-tartrate 2-amino-4,6-dimethoxypyrimidine (2ADT).


2011 ◽  
Vol 60 (3) ◽  
pp. 895-936
Author(s):  
Pierre Cardaliaguet ◽  
Olivier Ley ◽  
Aurelien Monteillet

1985 ◽  
Vol 26 (9) ◽  
pp. 1102-1111 ◽  
Author(s):  
A Kibe ◽  
M A Dudley ◽  
Z Halpern ◽  
M P Lynn ◽  
A C Breuer ◽  
...  

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