Abstract
Poly (ethylene glycol) (PEG) holding molecular weights around 7000 Da exhibits a double-lamella phenomenon on the surface replicas of bulk once-folding crystallization, whose mechanism is still unclear. Concerning to its specific hydrogen-bonding interactions at chain-ends, we performed dynamic Monte Carlo simulations to investigate the effects of specific chain-end interactions on once-folding crystallization of 16-mers. The results showed that the chain-end hydrogen-bonding interactions bring little effects to both kinetics of primary nucleation and lateral growth of chain-folded lamellar crystals but make a more significant terrace at the lateral growth front with a step of metastable once-folding towards the next step of stable chain-extending, raising the double-lamella phenomenon of their surface replicas. We found that the chain-end hydrogen-bonding interactions are rich at the surfaces of once-folded lamellar crystals, which thus enhance their metastability and retard their thickening into the chain-extended crystals. In addition, intra- and inter-molecular secondary nucleation at corresponding chain-folded and extended growth fronts show different growth rate dependences on the specific interaction strengths. Our results revealed the role of specific chain-end interactions in PEG crystallization.
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