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Complexity in Polymer Phase Transitions ---from Materials Science to Life Sciences Wenbing Hu ( 胡文兵 ) School of Chem. and Chem. Eng. Nanjing University CHINA 2008-05-20, Beijing
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What are polymers? Chain-like macromolecules containing 1000 atoms or more. ---1953 Nobel Laureate H. Stäudinger http://www.chemistryexplained.com/St-Te/Staudinger-Hermann.html
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Age of polymer materials Plastics (include foam plastics, thin films) Rubbers (tires, shoes, seals) Fibers (clothes, textures) Coatings (oil painting) Adhesives Water-absorbing and filtering resins Artificial organs ……
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Two basic phase transitions in polymer materials Liquid-liquid phase separation Polymer crystallization
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Liquid-liquid phase separation High-impact polystyrene (rubber-plastic blend) Soft & tough+Hard & crisp Hard & tough AFM picture by Jiang Liu
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Polymer crystallization Semi-crystalline contexture (solid+elastic) Hard & tough Hu, et al. Macromolecules 2003
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Semi-crystalline Plastics Fibers CellulosesStarchesChitosan
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Polymers belong to complex fluid Complexity: 32 definitions (Wikipedia) “Integration larger than addition.”
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Polymers belong to complex fluid Complexity: integration larger than addition. “ 1+1>2”
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Complexity in polymer phase transitions L-L phase separation + Crystallization Their interplay
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Phase diagrams of polymer solutions Interplay Competition and even more! L-L L-S L-S crystallization
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Molecular driving forces Mixing interactions B Drive New energy parameter! Classic Flory-Huggins parameter Flory J. Chem. Phys. 1942. Huggins Ann. N.Y. Acad. Sci. 1942. Polymer concentration T L-L L-S ?
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Why do we need new parameter? Phase diagrams in a single component
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In a single component Gas Liquid Solid Condensation Crystallization In polymer solutions Dilute Concentrated Crystalline Liquid-Liquid demixing Crystallization Molecular packing Packing energy: first stage L-L demixing second stage L-S crystallization
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Molecular driving forces Mixing interactions B Drive New energy parameter! Classic Flory-Huggins parameter Flory J. Chem. Phys. 1942. Huggins Ann. N.Y. Acad. Sci. 1942. Polymer concentration T L-L L-S Hu J. Chem. Phys. 2000. Parallel-packing interactions E p
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Partition function for polymer solutions Coordination number q,volume n,solvent takes n 1 sites,n 2 polymer chains, each taking r sites. Hu J. Chem. Phys. 113, 3901(2000); Hu et al. 118, 10343( 2003).
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Verify mean-field theory with simulations 32-mers at T(E p /E c, B/E c ) Theoretical predictions Simulation verifications Hu, W.-B.; Mathot, V.B.F; Frenkel, D. J. Chem. Phys. 118, 10343( 2003). L-L L-S
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The first story--- Crystal nucleation enhanced by L-L demixing.
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Crystallization influenced by L-L demixing L-S coexistence L-L binodal 1st 3rd 2nd Control the crystal morphology! Hu, W.-B.; Frenkel, D. Macromolecules 37, 4336(2004)
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Onset temperatures of crystal nucleation on cooling 128-mers in solutions C1 : B/E c =0.076,E p /E c =1 C2 : B/E c =0.03,E p /E c =1.072 C3 : B/E c =-0.1,E p /E c =1.275 Lines: crystal nucleation Dashes: L-L binodal Dots: L-L spinodal Zha, L.-Y.; Hu, W.-B. J. Phys. Chem. B 111, 11373-11378(2007). Crystal nucleation triggered by spinodal decomposition !
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Modulate morphology at low temperatures Triggered by prior SD No prior SD Zha, L.-Y.; Hu, W.-B. J. Phys. Chem. B 111, 11373-11378(2007).
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Crystal nucleation enhanced at the interfaces of incompatible polymers Ma, Y.; Zha, L.-Y.; Hu, W.-B.; Reiter G.; Han, C. C. Phys. Rev. E in press. 16-mers 50:50 blends, E P /E C =1, variable B/E C, kT/E C =4.0.
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Theoretical interpretation Ma, Y.; Zha, L.-Y.; Hu, W.-B.; Reiter G.; Han, C. C. Phys. Rev. E in press. L-S phase diagrams for variable B/E c L-S
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Something different in polymer solutions 128-mers , 50% , E p /E c =1,variable B/E c, kT/E c =4.5 Manuscript under preparation.
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Crystal nucleation enhanced at surfaces only with very poor solvent L-S phase diagrams for variable B/E c Manuscript under preparation.
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The second story--- L-L demixing enhanced by crystallizability.
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L-L demixing among isotactic, atactic and syndiotactic polypropylenes Mixing free energy of polymer blends: ~0 for r 1,r 2 >>1 ~0 for similar chemistry Component-selective crystallizability drives L-L demixing! Hu, W.-B.; Mathot, V.B.F. J. Chem. Phys. 119, 10953(2003). >0
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L-L demixing enhanced by fluctuations towards crystalline order Mean-field treatment Fluctuations? Ma, Y.; Hu, W.-B.; Wang, H. Phys. Rev. E 76, 031801(2007). 32-mers in 32 3 lattice E p /E c =1, variable B/E c Data points: simulations Lines: L-L binodals Dashes: L-S coexistence L-L L-S
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The third story--- Single-chain folding accelerated by collapse transition.
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Classification of polymer solutions Critical overlapping concentration C* Dilute solutions C C*
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Phase diagrams in single-chain systems Single 512-mer with variable B/E p Collapse transition T col Crystallization T cry Hu, W.-B.; Frenkel, D. J. Phys. Chem. B 110, 3734-7(2006)
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Free energy calculation at equilibrium T Height of free-energy barrier
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Crystal nucleation enhanced by prior collapse transition Hu, W.-B.; Frenkel, D. J. Phys. Chem. B 110, 3734-7(2006)
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Protein folding Levinthal paradox: It is formidable for protein folding to experience all possible conformation. The folding must have a fast path. Beta folding is a crystal nucleation process!
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1.Framework model via nucleation 2.Hydrophobic molten globule as intermediate 1+2=Nucleation-condensation model
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Fast path of protein folding
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Physics origin of life Life is a non-equilibrium phenomenon evolved in nature for dissipating energy more efficiently.
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Physics origin of life Life emerges at the edge of phase transitions with their interplay. The interplay provides adaptability and efficiency to bio-functions, for instance, the fast path of protein folding. Chain-like macromolecules are favorable for performing interplay.
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Summary Complexity in polymer phase transitions is represented by their interplay : 1 、 L-L demixing enhances crystal nucleation and thus modulates crystal morphology ; 2 、 Sometimes crystallizability enhances L-L demixing ; Fast path of protein folding may be based on this kind of interplay.
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Thanks for your attentions ! Discussions are welcome!
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