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- W2051570567 abstract "We describe simulations of a polymer melt sample containing 640 chains, each chain being composed of 100 methylene groups. Using these large scale simulations radii of gyration have been calculated with a statistical error of ∼2%. At this level of precision it is shown that even for this modest chain length configurational equilibrium is not achieved in less than 4 ns at 500 K. Values of the square radii of gyration, square end-to-end distances and proportion of conformers at equilibrium show good agreement with predictions of the Flory model of alkane chains in which all long range interactions along the chains are ignored. These simulations were performed using a Fujitsu AP1000 massively parallel processing machine with 1024 processors in conjunction with a recently described domain decomposition molecular dynamics algorithm [D. Brown, J. H. R. Clarke, M. Okuda, and T. Yamazaki, Comput. Phys. Commun. 83, 1 (1994)] capable of handling systems containing rigid bond constraints and threea are made with previous accurate data obtained for smaller samples containing just 10 n=100-site chains using the alternative cloning method of parallel processing [D. Brown, J. H. R. Clarke, M. Okuda, and T. Yamazaki, J. Chem. Phys. 100, 1684 (1994)]." @default.
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- W2051570567 date "1996-02-01" @default.
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- W2051570567 title "A large scale molecular dynamics study of chain configurations in the <i>n</i>=100 alkane melt" @default.
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- W2051570567 doi "https://doi.org/10.1063/1.470964" @default.
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