Scission-induced bounds on maximum polymer drag reduction in turbulent flow

被引:55
|
作者
Vanapalli, SA [1 ]
Islam, MT
Solomon, MJ
机构
[1] Univ Michigan, Dept Chem Engn, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Macromol Sci, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Engn Program, Ann Arbor, MI 48109 USA
关键词
D O I
10.1063/1.2042489
中图分类号
O3 [力学];
学科分类号
08 ; 0801 ;
摘要
We report the direct quantification of molar mass degradation in the drag- reducing polymers polyethylene oxide (PEO) and polyacrylamide (PAM) in turbulent pipe flows with an upstream tapered contraction. We find that entrance effects associated with the upstream contraction dominate the polymer degradation. Quantifying degradation according to the scaling relationship gamma(w) proportional to M-ws(-n), the exponent n is determined to be - 2.20 +/- 0.21 and - 2.73 +/- 0.18 for PEO and PAM, respectively. Here M-ws is the steady- state (or limiting) weight- average scission molar mass. A methodology is devised to circumvent polymer degradation due to the upstream contraction and thereby conduct degradation experiments in which only the turbulent flow in the pipe is responsible for chain scission. In this case, the scission- scaling relationship for PEO is gamma(w)proportional to M-w(-3.20 +/- 0.28). Here M-w is the degraded weight- average molar mass after one pass through the 1.63- m length of pipe. Based on these scaling relationships we obtain a new upper limit for polymer drag reduction that is determined by chain scission rather than the maximum drag reduction asymptote. (c) 2005 American Institute of Physics.
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页码:1 / 11
页数:11
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