Positron lifetime spectroscopy in ordered nanoporous polymers

被引:6
作者
Engbrecht, Jason [1 ]
Green, David [1 ]
Hillmyer, Marc A. [2 ]
Olson, David [2 ]
Todd, Eric M. [2 ]
机构
[1] St Olaf Coll, Dept Phys, Northfield, MN 55057 USA
[2] Univ Minnesota, Dept Chem, Minneapolis, MN 55455 USA
基金
美国国家科学基金会;
关键词
block copolymers; porosity; positron annihilation; positron lifetime spectroscopy; solid-state structure; structure-property relations; GLASS-TRANSITION; BLOCK-COPOLYMERS; ANNIHILATION; POLYSTYRENE; TEMPERATURE; NANOTECHNOLOGY; DEPENDENCE;
D O I
10.1002/polb.23314
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Positron annihilation lifetime spectroscopy (PALS) is a common technique used to characterize the porosity of polymers. Here, we expand its use to the study of ordered nanoporous polymer monoliths. Polystyrene (PS) monoliths with aligned cylindrical pores ranging in diameters from 15 to 35 nm were examined. Such large pores push the boundaries of the PALS technique. To achieve robust measurement, our system used larger detectors than those typically used for monolithic polymer samples. This was done to improve data rates while sacrificing timing resolution. Pore sizes determined using PALS were consistent with measurements made using small angle x-ray scattering. In addition, PALS was able to detect the collapse of the pores when the monolithic sample was heated above the Tg of PS. Because PALS measurements are not sensitive to the nature of the order within the structure nor are they, sensitive to the open or closed nature of the pores this technique could be expanded to a variety of other sample types. (c) 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2013, 51, 1157-1161
引用
收藏
页码:1157 / 1161
页数:5
相关论文
共 28 条
[1]   Block copolymers - Designer soft materials [J].
Bates, FS ;
Fredrickson, GH .
PHYSICS TODAY, 1999, 52 (02) :32-38
[2]   Common features in the formation of Ps, Mu, radiolytic hydrogen and solvated electrons in aqueous solutions [J].
Byakov, VM ;
Stepanov, SV .
JOURNAL OF RADIOANALYTICAL AND NUCLEAR CHEMISTRY-ARTICLES, 1996, 210 (02) :371-405
[3]  
Charlton M., 2001, POSITRON PHYS
[4]   Experimental verification of the blob model and delayed formation of Ps [J].
Dauwe, C ;
Van Waeyenberge, B ;
De Baerdemaeker, J .
ACTA PHYSICA POLONICA A, 2005, 107 (04) :623-628
[5]   Interface and surface effects on the glass transition in thin polystyrene films [J].
DeMaggio, GB ;
Frieze, WE ;
Gidley, DW ;
Zhu, M ;
Hristov, HA ;
Yee, AF .
PHYSICAL REVIEW LETTERS, 1997, 78 (08) :1524-1527
[6]   Determination of pore size in mesoporous thin films from the annihilation lifetime of positronium [J].
Dull, TL ;
Frieze, WE ;
Gidley, DW ;
Sun, JN ;
Yee, AF .
JOURNAL OF PHYSICAL CHEMISTRY B, 2001, 105 (20) :4657-4662
[7]   THE TEMPERATURE-DEPENDENCE OF POSITRON LIFETIMES IN SOLID PIVALIC ACID [J].
ELDRUP, M ;
LIGHTBODY, D ;
SHERWOOD, JN .
CHEMICAL PHYSICS, 1981, 63 (1-2) :51-58
[8]   Effect of free surfaces on the glass transition temperature of thin polymer films [J].
Forrest, JA ;
DalnokiVeress, K ;
Stevens, JR ;
Dutcher, JR .
PHYSICAL REVIEW LETTERS, 1996, 77 (10) :2002-2005
[9]   Dynamics of block copolymers: Theory and experiment [J].
Fredrickson, GH ;
Bates, FS .
ANNUAL REVIEW OF MATERIALS SCIENCE, 1996, 26 :501-550
[10]   Positron annihilation as a method to characterize porous materials [J].
Gidley, David W. ;
Peng, Hua-Gen ;
Vallery, Richard S. .
ANNUAL REVIEW OF MATERIALS RESEARCH, 2006, 36 :49-79