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Modification of the crystallization kinetics of a mixed bath of alkanes in the presence of coil-crystalline block copolymer ficelles

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Modification of the crystallization kinetics of a mixed bath of alkanes in the presence of coil-crystalline block copolymer ficelles. / Buzza, D. M.A.; McLeish, T. C.B.

In: Journal de Physique I, Vol. 7, No. 10, 01.12.1997, p. 1379-1392.

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Harvard

Buzza, DMA & McLeish, TCB 1997, 'Modification of the crystallization kinetics of a mixed bath of alkanes in the presence of coil-crystalline block copolymer ficelles', Journal de Physique I, vol. 7, no. 10, pp. 1379-1392.

APA

Buzza, D. M. A., & McLeish, T. C. B. (1997). Modification of the crystallization kinetics of a mixed bath of alkanes in the presence of coil-crystalline block copolymer ficelles. Journal de Physique I, 7(10), 1379-1392.

Vancouver

Buzza DMA, McLeish TCB. Modification of the crystallization kinetics of a mixed bath of alkanes in the presence of coil-crystalline block copolymer ficelles. Journal de Physique I. 1997 Dec 1;7(10):1379-1392.

Author

Buzza, D. M.A. ; McLeish, T. C.B. / Modification of the crystallization kinetics of a mixed bath of alkanes in the presence of coil-crystalline block copolymer ficelles. In: Journal de Physique I. 1997 ; Vol. 7, No. 10. pp. 1379-1392.

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@article{db516920d68c4bee977b5d67048693be,
title = "Modification of the crystallization kinetics of a mixed bath of alkanes in the presence of coil-crystalline block copolymer ficelles",
abstract = "Recent Neutron Scattering experiments by Richter et al. [1] show that the presence of coil-crystalline block copolymer (PE-PEP) micelles in a mixed alkane bath suppresses the crystallization out of solution of the long alkane component at low temperatures. Motivated by these experiments, we study theoretically the thermodynamics and kinetics of lamellar coil-crystalline block copolymer micelles in a bimodal solvent to better understand the factors determining the anti-precipitation action of coil-crystalline block copolymers. We assume an Alexander-de Gennes brush model for the strongly stretched corona chains and explicitly account for the polydispersity of the solvent chains. For the thermodynamic distribution of solvent chains in the corona, we find a predominance of short solvent chains to long solvent chains in the corona phase compared to the solvent bath, both with and without nematic interactions in the corona phase. We also calculate the rate of crystallization of the long solvent chains onto the micellar crystal core and find that the rate is sensitive to both brush and core parameters. In particular, we predict that to maximize the rate, both E{0\d/kTN& and Xn need to be made as small as possible, where Efoid is the folding energy of the crystal core chains, NA the number of statistical segments of the solvated corona chains and Xn parameterises the strength of nematic interactions in the micellar corona. This leads to the surprising result that for fixed E(0\d, the rate of crystallization is increased when we increase the molecular weight of the corona blocks. L",
author = "Buzza, {D. M.A.} and McLeish, {T. C.B.}",
year = "1997",
month = "12",
day = "1",
language = "English",
volume = "7",
pages = "1379--1392",
journal = "JOURNAL DE PHYSIQUE II",
issn = "1155-4312",
publisher = "Les Editions de Physique",
number = "10",

}

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TY - JOUR

T1 - Modification of the crystallization kinetics of a mixed bath of alkanes in the presence of coil-crystalline block copolymer ficelles

AU - Buzza, D. M.A.

AU - McLeish, T. C.B.

PY - 1997/12/1

Y1 - 1997/12/1

N2 - Recent Neutron Scattering experiments by Richter et al. [1] show that the presence of coil-crystalline block copolymer (PE-PEP) micelles in a mixed alkane bath suppresses the crystallization out of solution of the long alkane component at low temperatures. Motivated by these experiments, we study theoretically the thermodynamics and kinetics of lamellar coil-crystalline block copolymer micelles in a bimodal solvent to better understand the factors determining the anti-precipitation action of coil-crystalline block copolymers. We assume an Alexander-de Gennes brush model for the strongly stretched corona chains and explicitly account for the polydispersity of the solvent chains. For the thermodynamic distribution of solvent chains in the corona, we find a predominance of short solvent chains to long solvent chains in the corona phase compared to the solvent bath, both with and without nematic interactions in the corona phase. We also calculate the rate of crystallization of the long solvent chains onto the micellar crystal core and find that the rate is sensitive to both brush and core parameters. In particular, we predict that to maximize the rate, both E{0\d/kTN& and Xn need to be made as small as possible, where Efoid is the folding energy of the crystal core chains, NA the number of statistical segments of the solvated corona chains and Xn parameterises the strength of nematic interactions in the micellar corona. This leads to the surprising result that for fixed E(0\d, the rate of crystallization is increased when we increase the molecular weight of the corona blocks. L

AB - Recent Neutron Scattering experiments by Richter et al. [1] show that the presence of coil-crystalline block copolymer (PE-PEP) micelles in a mixed alkane bath suppresses the crystallization out of solution of the long alkane component at low temperatures. Motivated by these experiments, we study theoretically the thermodynamics and kinetics of lamellar coil-crystalline block copolymer micelles in a bimodal solvent to better understand the factors determining the anti-precipitation action of coil-crystalline block copolymers. We assume an Alexander-de Gennes brush model for the strongly stretched corona chains and explicitly account for the polydispersity of the solvent chains. For the thermodynamic distribution of solvent chains in the corona, we find a predominance of short solvent chains to long solvent chains in the corona phase compared to the solvent bath, both with and without nematic interactions in the corona phase. We also calculate the rate of crystallization of the long solvent chains onto the micellar crystal core and find that the rate is sensitive to both brush and core parameters. In particular, we predict that to maximize the rate, both E{0\d/kTN& and Xn need to be made as small as possible, where Efoid is the folding energy of the crystal core chains, NA the number of statistical segments of the solvated corona chains and Xn parameterises the strength of nematic interactions in the micellar corona. This leads to the surprising result that for fixed E(0\d, the rate of crystallization is increased when we increase the molecular weight of the corona blocks. L

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M3 - Article

VL - 7

SP - 1379

EP - 1392

JO - JOURNAL DE PHYSIQUE II

JF - JOURNAL DE PHYSIQUE II

SN - 1155-4312

IS - 10

ER -