CHEMICAL DERIVATIZATION AS A MEAN TO IMPROVE CONTACT-ANGLE GONIOMETRY OF CHEMICALLY HETEROGENOUS SURFACES

被引:8
作者
HOLLANDER, A [1 ]
BEHNISCH, J [1 ]
ZIMMERMANN, H [1 ]
机构
[1] FRAUNHOFER EINRICHTUNG ANGEW POLYMERFORSCH,KANTSTR 55,D-14513 TELTOW,GERMANY
关键词
CONTACT ANGLE GONIOMETRY; CHEMICAL DERIVATIZATION; PLASMA TREATMENT; POLYETHYLENE;
D O I
10.1002/pola.1994.080320408
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Plasma-oxidized polyethylene (0-PE) was derivatized with various chemicals and the advancing and receding contact angles with water, formamide, and tricresylphosphate were measured. The contact angles were used to evaluate the surface free energy (SFE) components in terms of the Lifshitz-van der Waals-acid base (LW-AB) model. The derivatization was directed to couple alkyl chains to carbonyl, hydroxyl, and carboxyl groups generated on the surface of O-PE. Carbonyl groups were treated with hydrazine and then reacted with dodecanoyl chloride. Hydroxyl groups were first reacted with reactive dicarboxylic acid dichlorides or cyanuric chloride, respectively, and then with alkylamines because the direct bonding of long-chain alkyl carboxylic acid chlorides proceeds slowly and is, therefore, completed by surface restructuring. Carboxyl groups were chlorinated and in a second step reacted with alkylamines. The bonding of C-12-alkyl chains can be sensitively detected by the LW part of the SFE. Concerning the receding contact angles, it is pointed out that the carbonyl groups are present on the surface in a higher concentration than hydroxyl and carboxyl groups. The combination of contact angle goniometry (CAG) and chemical derivatization reactions supplies semiquantitative information about functional groups in the uppermost surface layer. In this way, a major shortcoming of CAG can be overcome. (C) 1994 John Wiley & Sons, Inc.
引用
收藏
页码:699 / 709
页数:11
相关论文
共 25 条
[11]   ESCA STUDIES OF CORONA-DISCHARGE-TREATED POLYETHYLENE SURFACES BY USE OF GAS-PHASE DERIVATIZATION [J].
GERENSER, LJ ;
ELMAN, JF ;
MASON, MG ;
POCHAN, JM .
POLYMER, 1985, 26 (08) :1162-1166
[12]  
GIRAFALCO LA, 1957, J PHYS CHEM-US, V61, P904
[13]  
Gutmann V., 1978, DONOR ACCEPTOR APPRO
[14]  
HOLLANDER A, 1993, J APPL POLYM SCI, V649, P1857
[15]   SURFACE FREE-ENERGY COMPONENTS OF LIQUIDS AND LOW-ENERGY SOLIDS AND CONTACT ANGLES [J].
JANCZUK, B ;
BIALOPIOTROWICZ, T .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1989, 127 (01) :189-204
[16]   SURFACE DYNAMICS VS ADHESION IN OXYGEN PLASMA TREATED POLYOLEFINS [J].
MORRA, M ;
OCCHIELLO, E ;
GILA, L ;
GARBASSI, F .
JOURNAL OF ADHESION, 1990, 33 (1-2) :77-88
[17]   ESTIMATION OF SURFACE FREE ENERGY OF POLYMERS [J].
OWENS, DK ;
WENDT, RC .
JOURNAL OF APPLIED POLYMER SCIENCE, 1969, 13 (08) :1741-&
[18]   AN ESCA STUDY OF THE GAS-PHASE DERIVATIZATION OF POLY(ETHYLENE-TEREPHTHALATE) TREATED BY DRY-AIR AND DRY-NITROGEN CORONA DISCHARGE [J].
POCHAN, JM ;
GERENSER, LJ ;
ELMAN, JF .
POLYMER, 1986, 27 (07) :1058-1062
[19]  
SELL PJ, 1966, ANGEWANDTE CHEM, V78, P321
[20]   ESTIMATION OF THE POLAR PARAMETERS OF THE SURFACE-TENSION OF LIQUIDS BY CONTACT-ANGLE MEASUREMENTS ON GELS [J].
VANOSS, CJ ;
JU, L ;
CHAUDHURY, MK ;
GOOD, RJ .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1989, 128 (02) :313-319