Lecture

Ideal Polymer Chain: Size and Conformation

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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 theoretical treatment of the size and conformation of an ideal polymer chain, exploring concepts such as chain rigidity, polymer conformation, energy landscape, contour length, and polymer flexibility. It delves into the relationship between chain flexibility, bond angles, and bond rotation, as well as the characteristic ratio in chain rigidity. The presentation progresses to discuss the end-to-end distance, radius of gyration, and the freely rotating chain model. Additionally, it examines the deviations from ideal-chain behavior in real polymer chains, the representation of real chains by equivalent freely-jointed chains, and the Kuhn segment length as a measure of chain stiffness.

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Instructors (2)

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 (29)

Conformational isomerism

In chemistry, conformational isomerism is a form of stereoisomerism in which the isomers can be interconverted just by rotations about formally single bonds (refer to figure on single bond rotation). While any two arrangements of atoms in a molecule that differ by rotation about single bonds can be referred to as different conformations, conformations that correspond to local minima on the potential energy surface are specifically called conformational isomers or conformers.

Ideal chain

In polymer chemistry, an ideal chain (or freely-jointed chain) is the simplest model to describe polymers, such as nucleic acids and proteins. It assumes that the monomers in a polymer are located at the steps of a hypothetical random walker that does not remember its previous steps. By neglecting interactions among monomers, this model assumes that two (or more) monomers can occupy the same location. Although it is simple, its generality gives insight about the physics of polymers.

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.

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.

Polymerization

In polymer chemistry, polymerization (American English), or polymerisation (British English), is a process of reacting monomer molecules together in a chemical reaction to form polymer chains or three-dimensional networks. There are many forms of polymerization and different systems exist to categorize them. In chemical compounds, polymerization can occur via a variety of reaction mechanisms that vary in complexity due to the functional groups present in the reactants and their inherent steric effects.

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