Maximizing the grain growth rate during the disorder-to-order transition in block copolymer melts

The factors controlling grain growth during the disorder‐to‐order transition in a polystyrene‐block‐polyisoprene copolymer melt were studied with time‐resolved depolarized light scattering. The ordered phase consisted of hexagonally packed polyisoprene cylinders, and the order–disorder‐transition te...

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Veröffentlicht in:Journal of polymer science. Part B, Polymer physics Polymer physics, 2001-10, Vol.39 (19), p.2231-2242
Hauptverfasser: Kim, W. G., Garetz, B. A., Newstein, M. C., Balsara, N. P.
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container_issue 19
container_start_page 2231
container_title Journal of polymer science. Part B, Polymer physics
container_volume 39
creator Kim, W. G.
Garetz, B. A.
Newstein, M. C.
Balsara, N. P.
description The factors controlling grain growth during the disorder‐to‐order transition in a polystyrene‐block‐polyisoprene copolymer melt were studied with time‐resolved depolarized light scattering. The ordered phase consisted of hexagonally packed polyisoprene cylinders, and the order–disorder‐transition temperature of the block copolymer (TODT) was 132 ± 1 °C. Our objective was to identify the temperature at which the grain growth rate was maximized (Tmax) and compare it with theoretical predictions. We conducted seeded grain growth experiments, which comprised two steps. In the first step, which lasted for 43 min, the sample was cooled from the disordered state to 124 °C. This resulted in the formation of a small number of ordered grains or seeds. This was followed by a second step in which the sample was heated to temperatures between 124 and 132 °C and the seeds grew with time. Our objective was to study grain growth at different temperatures starting from the same initial condition. The value of Tmax obtained experimentally was 128 °C. The theoretically predicted value of Tmax, based entirely on the rheological properties of the disordered sample and TODT, was also 128 °C. © 2001 John Wiley & Sons, Inc. J Polym Sci Part B: Polym Phys 39: 2231–2242, 2001
doi_str_mv 10.1002/polb.1197
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G. ; Garetz, B. A. ; Newstein, M. C. ; Balsara, N. P.</creator><creatorcontrib>Kim, W. G. ; Garetz, B. A. ; Newstein, M. C. ; Balsara, N. P.</creatorcontrib><description>The factors controlling grain growth during the disorder‐to‐order transition in a polystyrene‐block‐polyisoprene copolymer melt were studied with time‐resolved depolarized light scattering. The ordered phase consisted of hexagonally packed polyisoprene cylinders, and the order–disorder‐transition temperature of the block copolymer (TODT) was 132 ± 1 °C. Our objective was to identify the temperature at which the grain growth rate was maximized (Tmax) and compare it with theoretical predictions. We conducted seeded grain growth experiments, which comprised two steps. In the first step, which lasted for 43 min, the sample was cooled from the disordered state to 124 °C. This resulted in the formation of a small number of ordered grains or seeds. 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In the first step, which lasted for 43 min, the sample was cooled from the disordered state to 124 °C. This resulted in the formation of a small number of ordered grains or seeds. This was followed by a second step in which the sample was heated to temperatures between 124 and 132 °C and the seeds grew with time. Our objective was to study grain growth at different temperatures starting from the same initial condition. The value of Tmax obtained experimentally was 128 °C. The theoretically predicted value of Tmax, based entirely on the rheological properties of the disordered sample and TODT, was also 128 °C. © 2001 John Wiley &amp; Sons, Inc. J Polym Sci Part B: Polym Phys 39: 2231–2242, 2001</description><subject>Applied sciences</subject><subject>block copolymers</subject><subject>Exact sciences and technology</subject><subject>grain growth</subject><subject>light scattering</subject><subject>ordering kinetics</subject><subject>Organic polymers</subject><subject>Physicochemistry of polymers</subject><subject>Properties and characterization</subject><subject>Thermal and thermodynamic properties</subject><issn>0887-6266</issn><issn>1099-0488</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><recordid>eNp1kL1OwzAUhS0EEqUw8AYZWBjS2nESxyOtoCAVysCPxGI5jt2aJnFlG7Xl6XFJgYnl-krnfEfXB4BzBAcIwmS4MnU5QIiSA9BDkNIYpkVxCHqwKEicJ3l-DE6ce4cwaBntAX7PN7rRn7qdR34ho7nlug3TrP0istzLqPqwP2KlnbGVtLE38fcSectbp702bRSwsjZiGQkTjtg2QW1k7d0pOFK8dvJs__bB88310_g2ns4md-OraSxwTkksCkFwRqs0UbRMEiwgLKtUJYpIDhNcSJULxBUsECkzTKuKUoWoKEVKCMayxH1w2eUKa5yzUrGV1Q23W4Yg23XDdt2wXTfBe9F5V9wJXqvwC6HdH4AgohQF27CzrXUtt__nscfZdLQPjjtCOy83vwS3S5YTTDL2-jBh-ejhDb-MUpbhL6bZhGk</recordid><startdate>20011001</startdate><enddate>20011001</enddate><creator>Kim, W. 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source Wiley Online Library Journals Frontfile Complete
subjects Applied sciences
block copolymers
Exact sciences and technology
grain growth
light scattering
ordering kinetics
Organic polymers
Physicochemistry of polymers
Properties and characterization
Thermal and thermodynamic properties
title Maximizing the grain growth rate during the disorder-to-order transition in block copolymer melts
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