Surface modification of Sylgard-184 poly(dimethyl siloxane) networks by ultraviolet and ultraviolet/ozone treatment

被引:734
作者
Efimenko, K
Wallace, WE
Genzer, J [1 ]
机构
[1] N Carolina State Univ, Dept Chem Engn, Raleigh, NC 27695 USA
[2] Natl Inst Stand & Technol, Div Polymers, Gaithersburg, MD 20899 USA
基金
美国国家科学基金会;
关键词
poly(dimethyl siloxane) networks; Sylgard-184; ultraviolet/ozone treatment; hydrophilic elastomers;
D O I
10.1006/jcis.2002.8594
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 [物理化学]; 081704 [应用化学];
摘要
We report on the surface modification of Sylgard-184 poly(dimethyl siloxane) (PDMS) networks by ultraviolet (UV) radiation and ultraviolet/ozone (UVO) treatment. The effects of the UV light wavelength and ambient conditions on the surface properties of Sylgard-184 are probed using a battery of experimental probes, including static contact angle measurements, Fourier transform infrared spectroscopy, near-edge X-ray absorption fine structure, and X-ray reflectivity. Our results reveal that when exposed to UV, the PDMS macromolecules in the surface region of Sylgard-184 undergo chain scission, involving both the main chain backbone and the side groups. The radicals formed during this process recombine and form a network whose wetting properties are similar to those of a UV-modified model PDMS. In contrast to the UV radiation, the UVO treatment causes very significant changes in the surface and near-surface structure of Sylgard-184. Specifically, the molecular oxygen and ozone created during the UVO process interact with the UV-modified specimen. As a result of these interactions, the surface of the sample contains a large number of hydrophilic (mainly-OH) groups. In addition, the material density within the first approximate to 5 nm reaches about 50% of that of pure silica. A major conclusion that can be drawn from the results and analysis described in this work is that the presence of the silica fillers in Sylgard-184 does not alter the surface properties of the UVO- and UV-modified Sylgard-184. (C) 2002 Elsevier Science (USA).
引用
收藏
页码:306 / 315
页数:10
相关论文
共 55 条
[1]
ANDERSON DR, 1974, ANAL SILICONES, P247
[2]
Spontaneous formation of ordered structures in thin films of metals supported on an elastomeric polymer [J].
Bowden, N ;
Brittain, S ;
Evans, AG ;
Hutchinson, JW ;
Whitesides, GM .
NATURE, 1998, 393 (6681) :146-149
[3]
The controlled formation of ordered, sinusoidal structures by plasma oxidation of an elastomeric polymer [J].
Bowden, N ;
Huck, WTS ;
Paul, KE ;
Whitesides, GM .
APPLIED PHYSICS LETTERS, 1999, 75 (17) :2557-2559
[4]
SURFACE FREE-ENERGIES OF ALKYLSILOXANE MONOLAYERS SUPPORTED ON ELASTOMERIC POLYDIMETHYLSILOXANES [J].
CHAUDHURY, MK .
JOURNAL OF ADHESION SCIENCE AND TECHNOLOGY, 1993, 7 (06) :669-675
[5]
Rate-dependent fracture at adhesive interface [J].
Chaudhury, MK .
JOURNAL OF PHYSICAL CHEMISTRY B, 1999, 103 (31) :6562-6566
[6]
CHAUDHURY MK, UNPUB
[7]
Spontaneous formation of complex and ordered structures on oxygen-plasma-treated elastomeric polydimethylsiloxane [J].
Chua, DBH ;
Ng, HT ;
Li, SFY .
APPLIED PHYSICS LETTERS, 2000, 76 (06) :721-723
[8]
PHOTODECOMPOSITION OF POLYMETHYLSILOXANE [J].
DELMAN, AD ;
LANDY, M ;
SIMMS, BB .
JOURNAL OF POLYMER SCIENCE PART A-1-POLYMER CHEMISTRY, 1969, 7 (12PA) :3375-&
[9]
Rapid prototyping of microfluidic switches in poly(dimethyl siloxane) and their actuation by electro-osmotic flow [J].
Duffy, DC ;
Schueller, OJA ;
Brittain, ST ;
Whitesides, GM .
JOURNAL OF MICROMECHANICS AND MICROENGINEERING, 1999, 9 (03) :211-217
[10]
EABORN C, 1960, ORGANOSILICON COMPOU