Reaction of methyl formate with VC(100) and TiC(100) surfaces

被引:11
作者
Frantz, P
Kim, HI
Didziulis, SV [1 ]
Li, S
Chen, ZY
Perry, SS
机构
[1] Aerosp Corp, Micro Nano Technol Dept, Space Mat lab, El Segundo, CA 90245 USA
[2] Univ Houston, Dept Chem, Houston, TX 77204 USA
关键词
vanadium carbide; titanium carbide; methyl formate; electron spectroscopies;
D O I
10.1016/j.susc.2005.09.010
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 chemistry of the (100) surface of the tribologically important materials vanadium carbide (VC) and titanium carbide (TiC) with methyl formate (CH3OCHO) has been studied with X-ray photoelectron spectroscopy (XPS), high resolution electron energy loss spectroscopy (HREELS), and temperature programmed desorption (TPD). The molecule reacts with each surface at temperatures below 150 K, although the extent of reaction is greater on the TiC surface. XPS and HREELS results indicate that the first step in this chemistry is the cleavage of the CH3O-CHO bond, generating surface methoxy groups (CH3O-) and either carbon monoxide on VC or a formyl (CHO) group on TiC. The methoxy group reacts further on both surfaces via pathways expected based on previous methanol adsorption studies, primarily decomposing through a formyl intermediate on VC to generate formaldehyde and evolving methanol on TiC. The formyl group formed directly from methyl formate on TiC enables the production and evolution of formaldehyde, and also appears to break down further to the elements. These results indicate a propensity for these carbides to react with esters, leading potentially to the beneficial formation of friction lowering surface films or the deleterious degradation of ester-based lubricants. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:144 / 162
页数:19
相关论文
共 26 条
[1]  
ACHWANER AL, 1997, J PHYS CHEM B, V101, P11112
[2]  
[Anonymous], 1983, INTRO PHOTOELECTRON
[3]  
AYRE CR, 1994, SURF SCI, V317, P65
[4]   WEAR-RESISTANT HARD TITANIUM CARBIDE COATINGS FOR SPACE APPLICATIONS [J].
BOVING, HJ ;
HINTERMANN, HE .
TRIBOLOGY INTERNATIONAL, 1990, 23 (02) :129-133
[5]   DIRECT VIBRATIONAL DETECTION OF SURFACE-REACTION CHANNELS LEADING TO CO DISSOCIATION AND TO ITS INHIBITION ON MO(110) [J].
CHEN, JG ;
COLAIANNI, ML ;
WEINBERG, WH ;
YATES, JT .
CHEMICAL PHYSICS LETTERS, 1991, 177 (02) :113-117
[6]   Small cluster models of the surface electronic structure and bonding properties of titanium carbide, vanadium carbide, and titanium nitride [J].
Didziulis, SV ;
Butcher, KD ;
Perry, SS .
INORGANIC CHEMISTRY, 2003, 42 (24) :7766-7781
[7]   PHOTOELECTRON SPECTROSCOPIC STUDIES OF THE ELECTRONIC-STRUCTURE AND BONDING IN TIC AND TIN [J].
DIDZIULIS, SV ;
LINCE, JR ;
STEWART, TB ;
EKLUND, EA .
INORGANIC CHEMISTRY, 1994, 33 (09) :1979-1991
[8]   Coordination chemistry of transition metal carbide surfaces: Detailed spectroscopic and theoretical investigations of CO adsorption on TiC and VC (100) surfaces [J].
Didziulis, SV ;
Frantz, P ;
Fernandez-Torres, LC ;
Guenard, RL ;
El-bjeirami, O ;
Perry, SS .
JOURNAL OF PHYSICAL CHEMISTRY B, 2001, 105 (22) :5196-5209
[9]   Substrate-dependent reactivity of water on metal carbide surfaces [J].
Didziulis, SV ;
Frantz, P ;
Perry, SS ;
El-bjeirami, O ;
Imaduddin, S ;
Merrill, PB .
JOURNAL OF PHYSICAL CHEMISTRY B, 1999, 103 (50) :11129-11140
[10]   STRUCTURE SENSITIVITY IN THE REACTION OF METHANOL ON ZRO2 [J].
DILARA, PA ;
VOHS, JM .
SURFACE SCIENCE, 1994, 321 (1-2) :8-18