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Lecture

Glassy State and Polymer Transition Temperatures

In course

MSE-360: Polymer science + TP

Introduction to polymer physics and the link between chemical structure and macroscopic properties, with emphasis on morphology and thermomechanical behaviour, polymer technology and manufacturing techniques, providing a basis for the rational selection of ...

Description

This lecture covers the glassy state in polymers, discussing the frozen ideal chain conformations and the Free Volume model. It also explores the relationship between the chemical structure of polymers and their glass transition temperature. The presentation delves into the amorphous state, polymer conformations, relaxation processes, and the unique energy dissipation mechanisms in polymer glasses. Additionally, it explains the concept of the glass transition temperature, its dependence on cooling rate, and the out-of-equilibrium nature of the glassy state. The lecture further examines factors impacting Tg, such as chain rigidity, plasticization, molecular weight, and cross-linking. It concludes with an overview of glass transition temperatures in linear polymers and the learning outcomes related to polymer interactions and Tg determination.

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Instructors (2)

Daniel Görl

John Christopher Plummer

ÉCOLE POLYTECHNIQUE FÉDÉRALE DE LAUSANNE (EPFL), Lausanne, Switzerland 1989- Collaborateur Scientifique/Chargé de Cours (Lecturer) (1998-) Privat Docent (1998) Laboratoire de Technologie des Composites et Polymères (LTC) (2000-) Laboratoire de Polymères (LP) (1998-2000) UNIVERSITY OF MICHIGAN (UMICH), Ann Arbor, MI, USA 1995-1996 Visiting Scientist, Department of Materials Science and Engineering (DMSE) UNIVERSITY OF CAMBRIDGE, Cambridge, UK 1986-1989 Research Assistant, Physics and Chemistry of Solids Group (PCS), Department of Physics UNIVERSITY OF CAMBRIDGE, Cambridge, UK, Department of Materials 1986 PhD, "Flux Pinning in Type-II Superconductors" UNIVERSITY OF CAMBRIDGE, Cambridge, UK, 1982 BA/MA Honours Degree in Natural Sciences Awards Prix R&R Haenny, 2007, DuPont Research Award, 2003, Commendation, British Polymer Group, Reading 1989 RECENT PUBLICATIONS Ramier J, Da Costa N, Plummer CJG, Leterrier Y, Manson JAE, Eckert R, Gaudiana R, Cohesion and adhesion of nanoporous TiO2 coatings on titanium wires for photovoltaic applications, Thin solid films, 516, 1913 (2008). Ramier J, Plummer CJG, Leterrier Y, Manson JAE, Eckert B, Gaudiana R, Mechanical integrity of dye-sensitized photovoltaic fibers, Renewable energy, 33, 314 (2008).

Houphouet-Boigny C, Plummer CJG, Wakeman MD, Manson JAE, Hybrid glass fiber-reinforced thermoplastic nanocomposites, J. Thermoplast. Comp. Mater., 21, 103 (2008).

Ternat C, Ouali L, Sommer H, Fieber W, Velazco MI, Plummer CJG, Kreutzer G, Klok HA, Manson JAE, Herrmann, Investigation of the Release of Bioactive Volatiles from Amphiphilic Multiarm Star-Block Copolymers by Thermogravimetry and Dynamic Headspace Analysis, Macromolecules 41(19), 7079 (2008). Ruggerone, R., Plummer, C.J.G., Negrete Herrera, N., Bourgeat-Lami, E., Månson, J-EA, Mechanical properties of highly filled latex-based polystyrene/laponite nanocomposites, Solid State Phenomena Vol. 151, 30 (2009). Plummer, CJG, Dalle Vacche, S, Houphouët-Boigny, C, Michaud, V, Månson, JAE, Hybrid Glass Mat Reinforced Polypropylene-Montmorillonite Nanocomposites, Solid State Phenomena Vol. 151, 60 (2009). Ruggerone, R., Plummer, C.J.G., Negrete Herrera, N., Bourgeat-Lami, E., Månson, J-EA, Highly filled polystyrenelaponite nanocomposites prepared by emulsion polymerization, European Polm. J. 45, 621 (2009). Ruggerone, R., Plummer, C.J.G., Negrete Herrera, N., Bourgeat-Lami, E., Månson, J-EA, Fracture mechanisms in polystyrene/laponite nanocomposites prepared by emulsion polymerization, Engineering Fracture Mechanics 76, 2846 (2009) Clausen P., Andreoni W., Curioni A., Hughs E., Plummer C.J.G. Adsorption of low-molecular-weight molecules on the surface of a sodium smectite clay: an ab initio study, Journal of Physical Chemistry C 113, 12293 (2009). Clausen P., Andreoni W., Curioni A., Hughs E., Plummer C.J.G., Water adsorption on a sodium smectite clay surface: an ab initio study, Journal of Physical Chemistry C 113, 15218 (2009). Molberg, M, Leterrier, Y., Plummer, C.J.G., Walder, C., Löwe, C., Opris, D.M., Nüesch, F.A., Bauer, S., Månson, J.-A.E., Frequency dependent dielectric and mechanical behaviour of elastomers for actuator applications, J. Appl. Phys. 106, 054112 (2009) Clausen P., Signorelli M., Schreiber A., Hughes E., Plummer CJG, Fessas D., Schiraldi A., Månson E. J.-A., Equilibrium desorption isotherms of water, ethanol, ethyl acetate and toluene on a sodium smectite clay, Journal of Thermal Analysis and Calorimetry 98, 833 (2009) Micusik, M., Bonnefond, A., Reyes, Y., Bogner, A., Chazeau, L., Plummer, C.J.G., Paulis, M., Leiza, J.R., Morphology of Polymer/Clay Latex Particles Synthesized by Miniemulsion Polymerization: Modeling and Experimental Results Macromol. React. Eng. 2010, 4, 432 (2010). Houphouet-Boigny C., Plummer CJG, Vacche SD, Michaud V, Wakeman MD, Månson E. J.-A., Hybrid Glass Mat-reinforced Polypropylene-Montmorillonite Nanocomposites, J. Comp. Mater. 44, 1975 (2010). Delabarde, C., Plummer C.J.G., Bourban, P.-E., Månson E. J.-A., Solidification behavior of PLLA/nHA nanocomposites, Comp. Sci. & Tech. 70, 1813 (2010). Plummer C.J.G., Ruggerone R., Negrete-Herrera N., Bourgeat-Lami E., Månson J.-A.E., Small Strain Mechanical Properties of Latex-Based Nanocomposite Films, Macromol. Symp. 294, 1 (2010). Dalle Vacche, S., Plummer C.J.G., Houphouet-Boigny C., Månson E. J.-A., Morphology and mechanical properties of isotactic polypropylene glass mat thermoplastic composites modified with organophilic montmorillonite, J Mater Sci 46, 2112 (2011).

Official source

Ontological neighbourhood

Chemistry

Organic chemistry: Polymer chemistry

Related concepts (32)

Polymer

A polymer (ˈpɒlᵻmər; Greek poly-, "many" + -mer, "part") is a substance or material consisting of very large molecules called macromolecules, composed of many repeating subunits. Due to their broad spectrum of properties, both synthetic and natural polymers play essential and ubiquitous roles in everyday life. Polymers range from familiar synthetic plastics such as polystyrene to natural biopolymers such as DNA and proteins that are fundamental to biological structure and function.

Glass transition

The glass–liquid transition, or glass transition, is the gradual and reversible transition in amorphous materials (or in amorphous regions within semicrystalline materials) from a hard and relatively brittle "glassy" state into a viscous or rubbery state as the temperature is increased. An amorphous solid that exhibits a glass transition is called a glass. The reverse transition, achieved by supercooling a viscous liquid into the glass state, is called vitrification.

Glass

Glass is a non-crystalline solid that is often transparent, brittle and chemically inert. It has widespread practical, technological, and decorative use in, for example, window panes, tableware, and optics. Glass is most often formed by rapid cooling (quenching) of the molten form; some glasses such as volcanic glass are naturally occurring. The most familiar, and historically the oldest, types of manufactured glass are "silicate glasses" based on the chemical compound silica (silicon dioxide, or quartz), the primary constituent of sand.

Polymer chemistry

Polymer chemistry is a sub-discipline of chemistry that focuses on the structures of chemicals, chemical synthesis, and chemical and physical properties of polymers and macromolecules. The principles and methods used within polymer chemistry are also applicable through a wide range of other chemistry sub-disciplines like organic chemistry, analytical chemistry, and physical chemistry. Many materials have polymeric structures, from fully inorganic metals and ceramics to DNA and other biological molecules.

Branching (polymer chemistry)

In polymer chemistry, branching is the regular or irregular attachment of side chains to a polymer's backbone chain. It occurs by the replacement of a substituent (e.g. a hydrogen atom) on a monomer subunit by another covalently-bonded chain of that polymer; or, in the case of a graft copolymer, by a chain of another type. Branched polymers have more compact and symmetrical molecular conformations, and exhibit intra-heterogeneous dynamical behavior with respect to the unbranched polymers.

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