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Catalyst cobalt-molybdate COMO

Impregnation of cobalt and molybdenum (without sodium) increases largely the isomerizing activity of the catalyst the /3-pinene is then completely converted. The catalysts prepared with sodium molybdate and sodium hydroxide (Co-Mo-Na and Na-Co-Mo-Na) have lower isomerizing activities while their HDS activities are significantly increased. As in the case of alumina supported catalysts the sulfided CoMo phase protected by a double layer of alkaline ions on the carbon support gives the best results in HDS of /3-pinene. The behaviour of this catalyst was examined in desulfurization of the turpentine oil (40% a-pinene, 25% /3-pinene, 25% A -carene and 10% camphene + dipentene + myrcene, 1500 ppm S). The results are recorded in Table 6. [Pg.207]

Such an effect might be expected when boehmite supported cobalt is being calcined, viz. during the phase transition AIO(OH) - y-Al203. Figure 7 shows spectra of pyridine, adsorbed on the sample CoMo-124 B, which has been prepared in this way. Spectra for MoCo-122, -123 and -124, containing 2, 3 and 4 wt% CoO resp. are shown for comparison. All these catalysts have had a final calcination of 650°C. Comparison of the spectra of CoMo-124 B and MoCo-124 indicates that the intensity of the 1612 cm l band, which is introduced by the interaction of the cobalt ions and the molybdate layer, is lower for CoMo-124 B than for MoCo-124. The spectrum for CoMo-124 B resembles that of CoMo-123, indicating that a part of the cobalt ions does not participate in this interaction. [Pg.160]


See other pages where Catalyst cobalt-molybdate COMO is mentioned: [Pg.719]    [Pg.1047]    [Pg.325]    [Pg.227]    [Pg.202]    [Pg.583]    [Pg.324]   
See also in sourсe #XX -- [ Pg.207 , Pg.210 ]




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