The surface chemistry resulting from low-pressure plasma treatment of polystyrene: The effect of residual vessel bound oxygen

被引:52
作者
Dhayal, Marshal
Alexander, Morgan R.
Bradley, James W.
机构
[1] UMIST, Dept Phys, Manchester M60 1QD, Lancs, England
[2] UMIST, Ctr Corros & Protect, Manchester M60 1QD, Lancs, England
关键词
plasma; low-pressure; polymer; surface treatment; modification; XPS; base-pressure; residual water; vacuum;
D O I
10.1016/j.apsusc.2005.10.005
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 surface chemistry of plasma treated polystyrene samples has been studied in a specially designed low-pressure argon discharge system incorporating in situ XPS analysis. By using an electrostatic grid biasing technique, the plasma source can also be used in a mode preventing ion interactions with the sample. The system, which utilizes a vacuum transfer chamber between plasma and XPS analysis has allowed us to differentiate between the level of oxygen incorporated at the polystyrene surface from residual gas during treatment and that from the exposure of the treated sample to the laboratory atmosphere. Using typical base pressures of about 5 x 10(-3) Pa(4 x 10(-5) Torr) the XPS results show that significant oxygen surface incorporation resulted from oxygen containing species in the plasma itself (i.e. water vapour with 2 x 10(-3) Pa partial pressure). The surface concentration of O was measured at 7.6 at.%. Subsequent atmospheric exposure of the treated samples resulted in only a small increase (of 0.6 at.%) in oxygen incorporation in the form of acid anhydride functionalities. XPS measurements of PS samples exposed to plasmas with no ion-surface component (i.e. exposure from VUV, UV and excited neutral species only) showed no appreciable change in oxygen incorporation compared to those with low-energy ion bombardment from the plasma (< 20 eV). Given the energetics of the remaining bombarding species, it indicates that VUV radiation may be chiefly responsible for the production of free radical sites in this discharge regime. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:7957 / 7963
页数:7
相关论文
共 14 条
[1]   An in situ comparison between VUV photon and ion energy fluxes to polymer surfaces immersed in an RF plasma [J].
Barton, D ;
Bradley, JW ;
Gibson, KJ ;
Steele, DA ;
Short, RD .
JOURNAL OF PHYSICAL CHEMISTRY B, 2000, 104 (30) :7150-7153
[2]  
Beamson G., 1992, ADV MATER, DOI DOI 10.1002/ADMA.19930051035
[3]   ESCA APPLIED TO POLYMERS .15. RF GLOW-DISCHARGE MODIFICATION OF POLYMERS, STUDIED BY MEANS OF ESCA IN TERMS OF A DIRECT AND RADIATIVE ENERGY-TRANSFER MODEL [J].
CLARK, DT ;
DILKS, A .
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 1977, 15 (10) :2321-2345
[4]   Investigating the plasma surface modification of polystyrene at low ion power densities [J].
Dhayal, M ;
Parry, KL ;
Short, RA ;
Bradley, JW .
JOURNAL OF PHYSICAL CHEMISTRY B, 2004, 108 (37) :14000-14004
[5]   Using heated probes in plasma polymerising discharges [J].
Dhayal, M ;
Bradley, JW .
SURFACE & COATINGS TECHNOLOGY, 2004, 184 (01) :116-122
[6]   Using an afterglow plasma to modify frequency (RF) polystyrene surfaces in pulsed radio argon discharges [J].
Dhayal, M ;
Forder, D ;
Parry, KL ;
Short, RD ;
Bradley, JW .
SURFACE & COATINGS TECHNOLOGY, 2003, 174 :872-876
[7]   Electron temperature control in low-pressure plasmas using a two-mesh-separation technique [J].
Dhayal, M ;
Forder, D ;
Short, RD ;
Bradley, JW .
VACUUM, 2003, 70 (01) :67-71
[8]   Tailored plasmas for applications in the surface treatment of materials [J].
Dhayal, M ;
Forder, D ;
Parry, K ;
Short, RD ;
Barton, D ;
Bradley, JW .
SURFACE & COATINGS TECHNOLOGY, 2003, 162 (2-3) :294-300
[9]   XPS STUDIES OF IN-SITU PLASMA-MODIFIED POLYMER SURFACES [J].
GERENSER, LJ .
JOURNAL OF ADHESION SCIENCE AND TECHNOLOGY, 1993, 7 (10) :1019-1040
[10]   INTERACTION OF LOW-ENERGY IONS (LESS-THAN-10 EV) WITH POLYMETHYLMETHACRYLATE DURING PLASMA TREATMENT [J].
GRONING, P ;
KUTTEL, OM ;
COLLAUDCOEN, M ;
DIETLER, G ;
SCHLAPBACH, L .
APPLIED SURFACE SCIENCE, 1995, 89 (01) :83-91