Swelling responses of surface- attached bottlebrush polymer networks

被引:10
作者
Mah, Adeline Huizhen [1 ,2 ]
Mei, Hao [3 ]
Basu, Prithvi [4 ]
Laws, Travis S. [5 ]
Ruchhoeft, Paul [4 ]
Verduzco, Rafael [3 ]
Stein, Gila E. [5 ]
机构
[1] Univ Houston, Mat Sci & Engn Program, Houston, TX 77204 USA
[2] Univ Houston, Dept Chem & Biomol Engn, Houston, TX 77204 USA
[3] Rice Univ, Dept Chem & Biomol Engn, Houston, TX 77006 USA
[4] Univ Houston, Dept Elect & Comp Engn, Houston, TX USA
[5] Univ Tennessee, Dept Chem & Biomol Engn, Knoxville, TN 37996 USA
基金
美国国家科学基金会;
关键词
CYLINDRICAL MOLECULAR BRUSHES; HYDROGELS; LITHOGRAPHY; ELASTOMERS; COPOLYMERS; DEPENDENCE; BEHAVIOR; DENSITY; WEIGHT; FILMS;
D O I
10.1039/c8sm01127c
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The swelling responses of thin polymer networks were examined as a function of primary polymer architecture. Thin films of linear or bottlebrush polystyrene were cast on polystyrene-grafted substrates, and surface-attached networks were prepared with a radiation crosslinking reaction. The dry and equilibrated swollen thicknesses were both determined with spectroscopic ellipsometry. The dry thickness, which reflects the insoluble fraction of the film after crosslinking, depends on the primary polymer size and radiation dose but is largely independent of primary polymer architecture. When networks are synthesized with a high radiation dose, producing a high density of crosslinks, the extent of swelling is similar for all primary polymer architectures and molecular weights. However, when networks are synthesized with a low radiation dose, the extent of swelling is reduced as the primary polymer becomes larger or increasingly branched. These trends are consistent with a simple Flory model for equilibrium swelling that describes the effects of branch junctions and radiation crosslinks on network elasticity.
引用
收藏
页码:6728 / 6736
页数:9
相关论文
共 50 条
[1]   Fluorescence study on the swelling behavior of comb-type grafted poly(N-isopropylacrylamide) hydrogels [J].
Annaka, M ;
Tanaka, C ;
Nakahira, T ;
Sugiyama, M ;
Aoyagi, T ;
Okano, T .
MACROMOLECULES, 2002, 35 (21) :8173-8179
[2]  
Barton A.F. M., 1990, HDB POLYM LIQUID INT
[3]  
Brandrup J., 1999, POLYM HDB, V2
[4]   Soft Poly(dimethylsiloxane) Elastomers from Architecture-Driven Entanglement Free Design [J].
Cai, Li-Heng ;
Kodger, Thomas E. ;
Guerra, Rodrigo E. ;
Pegoraro, Adrian F. ;
Rubinstein, Michael ;
Weitz, David A. .
ADVANCED MATERIALS, 2015, 27 (35) :5132-5140
[5]   Two-Dimensional Photonic Crystal Chemical and Biomolecular Sensors [J].
Cai, Zhongyu ;
Smith, Natasha L. ;
Zhang, Jian-Tao ;
Asher, Sanford A. .
ANALYTICAL CHEMISTRY, 2015, 87 (10) :5013-5025
[6]  
Chen W-L., 2017, 50th Anniversary Perspective: Polymer Brushes: Novel Surfaces for Future Materials, DOI [DOI 10.1021/ACS.MACROMOL.7B00450, 10.1021/acs.macromol.7b00450]
[7]  
Cheremisinoff N.P., 1989, HDB POLYM SCI TECHNO
[8]   NETWORK STRUCTURES OF RADIATION-CROSS-LINKED STAR POLYMER GELS [J].
CIMA, LG ;
LOPINA, ST .
MACROMOLECULES, 1995, 28 (20) :6787-6794
[9]   Analyte-Responsive Hydrogels: Intelligent Materials for Biosensing and Drug Delivery [J].
Culver, Heidi R. ;
Clegg, John R. ;
Peppas, Nicholas A. .
ACCOUNTS OF CHEMICAL RESEARCH, 2017, 50 (02) :170-178
[10]   Molecular Weight Dependence of Zero-Shear Viscosity in Atactic Polypropylene Bottlebrush Polymers [J].
Dalsin, Samuel J. ;
Hillmyer, Marc A. ;
Bates, Frank S. .
ACS MACRO LETTERS, 2014, 3 (05) :423-427