SYNERGY BETWEEN THE COMOS PHASE AND SUPPORTED OR UNSUPPORTED COBALT SULFIDE - EXISTENCE OF A REMOTE-CONTROL EFFECT

Citation
M. Karroua et al., SYNERGY BETWEEN THE COMOS PHASE AND SUPPORTED OR UNSUPPORTED COBALT SULFIDE - EXISTENCE OF A REMOTE-CONTROL EFFECT, Bulletin of the Chemical Society of Japan, 68(1), 1995, pp. 107-119
Citations number
74
Categorie Soggetti
Chemistry
ISSN journal
00092673
Volume
68
Issue
1
Year of publication
1995
Pages
107 - 119
Database
ISI
SICI code
0009-2673(1995)68:1<107:SBTCPA>2.0.ZU;2-U
Abstract
Unsupported Co9S8, MoS2, and CoMoS sulfides (prepared by the HSP metho d) as well as supported MoS2/Al2O3 and CoSx/C (prepared by impregnatio n) were used to prepare a series of binary mechanical mixtures of vari ous compositions. A variety of physicochemical techniques (temperature programmed decomposition and sulfidation, both followed by subsequent TPO, XRD, TPR, microelectrophoresis, XPS and AEM) were used to study the samples, verify the formation of the ''CoMoS phase'' in the mixed CoMo sulfide and investigate the existence of interactions between the sulfides forming the mechanical mixtures. The catalytic activity of t he supported and unsupported HSP sulfides as well as that of the mecha nical mixtures was tested in the hydrodesulfurization of thiophene (HD S) and the hydrogenation of cyclohexene (HYD) at 513 K and 3 MPa. The mechanical mixtures exhibit a synergy in HDS and HYD. This shows that cobalt sulfide (supported or unsupported HSP) can promote the activity not only of molybdenum sulfide, but also of the unsupported HSP ''CoM oS phase''. In addition, XRD and AEM (performed before and after catal ytic tests) were used to study the evolution of the unsupported ''CoMo S phase'' during the catalytic reaction, ft was found that this phase is unstable; cobalt segregates from the CoMoS association to form Co9S 8, even after a relatively short period in the reactor. These results provide more evidence that the remote control mechanism plays a major role in the synergetic behavior of the CoMo hydrotreating catalysts.