Copolymers are polymers that are synthesized with more than one kind of repeat unit (or monomer). It exhibits a gradual change in monomer composition from predominantly one species to predominantly the other[1], unlike with block copolymers, which have an abrupt change in composition[2], and random copolymers, which have no continuous change in composition (see Figure 1).[3] [4] In the gradient copolymer, as a result of the gradual compositional change along the length of the polymer chain less intrachain and interchain repulsion are observed.[5]
The development of controlled radical polymerization as a synthetic methodology in the 1990’s allowed for increased study of the concepts and properties of gradient copolymers because the synthesis of this group of novel polymers was now straightforward.
Due to the similar properties of gradient copolymers to that of block copolymers, they have been considered as a cost effective alternative in applications for other preexisting copolymers.[2]
Polymer Composition
edit
In the gradient copolymer, there is a continuous change in monomer composition along the polymer chain (see Figure 2). This change in composition can be depicted in a mathematical expression.The local composition gradient fraction is described by molar fraction of monomer 1 in the copolymer and degree of polymerization and its relationship is as follows[2]:
The above equation supposes all of the local monomer composition is continuous. To make up for this assumption, another equation of ensemble average is used:[2]
The refers ensemble average of the local chain composition, refers degree of polymerization, refers number of polymer chains in the sample and refers composition of polymer chain i at position .
This second equation identifies the average composition over all present polymer chains at a given position, .[2]
Synthesis
editPrior to the development of controlled radical polymerization (CRP), gradient copolymers (as distinguished from statistical copolymers) were not synthetically possible. While a "gradient" can be achieved through compositional drift due to a difference in reactivity of the two monomers, this drift will not encompass the entire possible compositional range. All of the common CRP methods[6] including atom transfer radical polymerization and Reversible addition−fragmentation chain transfer polymerization as well as other living polymerization techniques including anionic addition polymerization and ring-opening polymerization have been used to synthesize gradient copolymers.[2]
The gradient can be formed through either a spontaneous or a forced gradient. Spontaneous gradient polymerization is due to a difference in reactivity of the monomers. The resulting change in composition throughout the polymerization creates an inconsistent gradient along the polymer. Forced gradient polymerization involves varying the comonomer composition of the feed being throughout the reaction time. Because the rate of addition of the second monomer influences the polymerization and therefore properties of the formed polymer, continuous information about the polymer composition is vital. The online compositional information is often gathered through automatic continuous online monitoring of polymerization reactions, a process which provides in situ information allowing for constant composition adjustment to achieve the desired gradient composition.
Properties of Gradient Copolymers
editThe wide range of composition possible in a gradient polymer due to the variety of monomers incorporated and the change of the composition results in a large variety of properties. In general, the glass transition temperature (Tg) is broad in comparison with the homopolymers. Micelles of the gradient copolymer can form when the gradient copolymer concentration is too high in a block copolymer solution. As the micelles form, the micelle diameter actually shrinks creating a "reel in" effect. The general structure of these copolymers in solution is not yet well established.
The composition can be determined by gel permeation chromatography(GPC) and nuclear magnetic resonance (NMR). Generally the composition has a narrow polydispersity index (PDI) and the molecular weight increases with time as the polymer forms.
Applications of Gradient Copolymers
edit- Compatibilizing Phase-Separated Polymer Blends
For the compatiabilization of immiscible blends, the gradient copolymer can be used by improving mechanical and optical properties of immiscible polymers and decreasing its dispersed phase to droplet size.[7] The compatibilization has been tested by reduction in interfacial tension and steric hindrance against coalescence. This application is not available for block and graft copolymer because of its very low critical micelle concentration (cmc). However, the gradient copolymer, which has higher cmc and exhibits a broader interfacial coverage, can be applied to effective blend compatibilizers.[8]
A small amount of gradient copolymer (i.e.styrene/4-hydroxystyrene) is added to a polymer blend (i.e. polystyrene/polycaprolactone) during melt processing. The resulting interfacial copolymer helps to stabilize the dispersed phase due to the hydrogen-bonding effects of hydroxylstyrene with the polycaprolactone ester group.
- Impact Modifiers and Sound or Vibration Dampers
The gradient copolymer have very broad glass transition temperature (Tg) in comparison with other copolymers, at least four times bigger than that of a random copolymer. This broad glass transition is one of the important features for vibration and acoustic damping applications.[5] Since, in this temperature region, energy dissipation has a maximized value.[2] The glass transition breadth can be adjusted by selection of monomers with different degrees of reactivity in their controlled radical polymerization (CRP). The strongly segregated styrene/4-hydroxystyrene (S/HS) gradient copolymer is used to study damping properties due to its unusual broad glass transition breadth.[5]
- Potential applications
There are many possible applications for gradient copolymer like pressure sensitive adhesives, wetting agent, coating, or dispersion. However, these applications are not proved about its practical performance and stability as gradient copolymers.[2]
Resources
edithttp://torkelson.northwestern.edu/Research/GCP/gcp.html
http://www.cmu.edu/maty/materials/index.html
References
edit- ^ Kryszewski, M (1998). "Gradient Polymers and Copolymers". Polymers for Advanced Technologies. 9 (4). John Wiley & Sons, Ltd.: 224–259. doi:10.1002/(SICI)1099-1581(199804)9:4<244::AID-PAT748>3.0.CO;2-J. ISSN 1042-7147.
- ^ a b c d e f g h Beginn, Uwe (2008). "Gradient Copolymer". Colloid Polym Sci. 286 (13). Springer: 1465–1474. doi:10.1007/s00396-008-1922-y. Cite error: The named reference "A" was defined multiple times with different content (see the help page).
- ^ Matyjaszewski, Krzyszytof (2000). "Gradient Copolymers by Atom Transfer Radical Copolymerization". J. Phys. Org. Chem. 13. John Wiley & Sons, Ltd.: 775–786. doi:10.1002/1099-1395 (inactive 2023-08-02).
{{cite journal}}: Unknown parameter|coauthors=ignored (|author=suggested) (help)CS1 maint: DOI inactive as of August 2023 (link) - ^ Cowie, J.M.G. (2008). Polymers: Chemistry and Physics of Modern Materials (Third ed.). CRC Press. pp. 147–148. ISSN 8493-9813.
{{cite book}}: Check|issn=value (help); Unknown parameter|coauthors=ignored (|author=suggested) (help) - ^ a b c Mok, Michelle (2008). "Gradient Copolymers with Broad Glass Transition Temperature Regions: Design of Purely Interphase Compositions for Damping Applications". Journal of Polymer Science. 46. Wiley Periodicals, Inc.: 48–58. doi:10.1002/polb (inactive 2023-08-02).
{{cite journal}}: Unknown parameter|coauthors=ignored (|author=suggested) (help)CS1 maint: DOI inactive as of August 2023 (link) Cite error: The named reference "E" was defined multiple times with different content (see the help page). - ^ Davis, Kelly A.; Matyjaszewski, Krzysztof (2002). "Statistical, Gradient, Block, and Graft Copolymers by Controlled/Living Radical Polymerizations". Advanced in Polymer Science. Advances in Polymer Science. 159. Springer: 1–13. doi:10.1007/3-540-45806-9_1. ISBN 978-3-540-43244-9.
- ^ Ramic, Anthony J.; Stehlin, Julia C.; Hudson, Steven D.; Jamieson, Alexander M.; Manas-Zloczower, Ica (2000). "Influence of Block Copolymer on Droplet Brekup and Coalescence in Model Immiscible Polymer Blends". Macromolecules. 33 (2). American Chemical Society: 371–374. doi:10.1021/ma990420c.
- ^ Kim, Jungki; Gray, Maisha K.; Zhou, Hongying; Nguyen, Sonbinh T.; Torkelson, John M. (Feb, 22, 2005). "Polymer Blend Compatibilization by Gradient Copolymer Addition during Melt Processing: Stabilization nof Dispersed Phase to Static Coarsening". Macromolecules. 38 (4). American Chemical Society: 1037–1040. doi:10.1021/ma047549t.
{{cite journal}}: Check date values in:|date=(help)