Surface treatment of calcite with fatty acids: Structure and properties of the organic monolayer

被引:153
作者
Osman, MA [1 ]
Suter, UW [1 ]
机构
[1] ETH Ctr, Dept Mat, Inst Polymer, CH-8092 Zurich, Switzerland
关键词
D O I
10.1021/cm021222u
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
Thermogravimetric analysis was used to investigate the surface cleanliness of calcite fillers and to determine the optimal amount of fatty acid needed to coat the particles with an organic monolayer. The use of excess surfactant led to the formation of a bilayer as well as to the presence of free acid molecules. Both species could be detected by TGA. Optimal coating of calcite with stearic acid gave a monolayer of calcium stearate bicarbonate in which one acid molecule is attached to every Ca2+ present on the surface. The alkyl chains in the monolayer are vertically oriented to the surface and are restricted in their motion. C-13 NMR and IR spectroscopy revealed that the chain conformation shows a high trans population, which leads to an ordered solidlike phase. Monolayers of saturated fatty acids with long alkyl chains (greater than or equal toC(10)) showed similar behavior, while the lower homologues ( greater than or equal toC(10)) gave monolayers with dynamically disordered phases. The immobilization of oleic acid molecules by tethering them to the calcite surface rendered them liable to thermal polymerization at relatively low temperatures. In other words, calcite can be coated with a monolayer of oleic acid molecules, which is polymerized later to give a polymeric monolayer.
引用
收藏
页码:4408 / 4415
页数:8
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共 43 条
[1]   The influence of surface energetics of calcium carbonate minerals on mineral-polymer interaction in polyolefin composites [J].
Ahsan, T ;
Taylor, DA .
JOURNAL OF ADHESION, 1998, 67 (1-4) :69-79
[2]   Structure and chain dynamics of alkanethiol-capped gold colloids [J].
Badia, A ;
Gao, W ;
Singh, S ;
Demers, L ;
Cuccia, L ;
Reven, L .
LANGMUIR, 1996, 12 (05) :1262-1269
[3]   Self-assembled monolayers on gold nanoparticles [J].
Badia, A ;
Singh, S ;
Demers, L ;
Cuccia, L ;
Brown, GR ;
Lennox, RB .
CHEMISTRY-A EUROPEAN JOURNAL, 1996, 2 (03) :359-363
[4]   A RAMAN AND INFRARED SPECTROSCOPIC STUDY OF COMPOUNDS CHARACTERIZED BY STRONG HYDROGEN-BONDS [J].
BERTOLUZZA, A ;
MONTI, P ;
MORELLI, MA ;
BATTAGLIA, MA .
JOURNAL OF MOLECULAR STRUCTURE, 1981, 73 (APR) :19-29
[5]   ACCURATE SUBMICRON PARTICLE-SIZE MEASUREMENT OF ALUMINA AND QUARTZ POWDERS USING A CUVETTE PHOTOCENTRIFUGE [J].
BOWEN, P ;
HERARD, C ;
HUMPHRYBAKER, R ;
SATO, E .
POWDER TECHNOLOGY, 1994, 81 (03) :235-240
[6]   INFRARED SPECTROSCOPIC IDENTIFICATION OF SPECIES ARISING FROM REACTIVE ADSORPTION OF CARBON OXIDES ON METAL-OXIDE SURFACES [J].
BUSCA, G ;
LORENZELLI, V .
MATERIALS CHEMISTRY, 1982, 7 (01) :89-126
[7]   Surface coverage and its determination: Role of acid-base interactions in the surface treatment of mineral fillers [J].
Fekete, E ;
Pukanszky, B .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1997, 194 (02) :269-275
[8]   SURFACE MODIFICATION AND CHARACTERIZATION OF PARTICULATE MINERAL FILLERS [J].
FEKETE, E ;
PUKANSZKY, B ;
TOTH, A ;
BERTOTI, I .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1990, 135 (01) :200-208
[9]   Structure and growth of stearate monolayers on calcite: First results of an in situ X-ray reflectivity study [J].
Fenter, P ;
Sturchio, NC .
GEOCHIMICA ET COSMOCHIMICA ACTA, 1999, 63 (19-20) :3145-3152
[10]   Characterization of coated particulate fillers [J].
Gilbert, M ;
Sutherland, I ;
Guest, A .
JOURNAL OF MATERIALS SCIENCE, 2000, 35 (02) :391-397