Cobalt molybdenum containing

The conversion of CO to CO2 can be conducted in two different ways. In the first, gases leaving the gas scmbber are heated to 260°C and passed over a cobalt—molybdenum catalyst. These catalysts typically contain 3—4% cobalt(II) oxide [1307-96-6] CoO 13—15% molybdenum oxide [1313-27-5] MoO and 76—80% alumina, JSifDy and are offered as 3-mm extmsions, SV about 1000 h . On these catalysts any COS and CS2 are converted to H2S. Operating temperatures are 260—450°C. The gases leaving this shift converter are then scmbbed with a solvent as in the desulfurization step. After the first removal of the acid gases, a second shift step reduces the CO content in the gas to 0.25—0.4%, on a dry gas basis. The catalyst for this step is usually Cu—Zn, which may be protected by a layer of ZnO. 

The first iron—nickel martensitic alloys contained ca 0.01% carbon, 20 or 25% nickel, and 1.5—2.5% aluminum and titanium. Later an 18% nickel steel containing cobalt, molybdenum, and titanium was developed, and still more recentiy a senes of 12% nickel steels containing chromium and molybdenum came on the market. 

Ferroflning A mild hydrotreating process for purifying lubricating oils. The catalyst contained cobalt, molybdenum, and iron (hence the name). Developed by the British Petroleum Company and first operated in Dunkirk, England in 1961. 

These heterogeneous catalysis contain nickel, cobalt, molybdenum, tungsten, platinum, or palladium on acidic aluminum silicate or zeolite supports. As with reforming catalysts, the catalysts here are also believed to be... 

The most important raw materials for the production of non-ferrous metals, such as copper, lead, zinc, nickel, cobalt, molybdenum, antimony and cadmium, are the sulfide minerals. The use of collectors containing various thio-type functional groups has proved to be the most successful in the flotation of these minerals. Some of these compounds are shown in Table 1. 

Molybdenum oxide - alumina systems have been studied in detail (4-8). Several authors have pointed out that a molybdate surface layer is formed, due to an interaction between molybdenum oxide and the alumina support (9-11). Richardson (12) studied the structural form of cobalt in several oxidic cobalt-molybdenum-alumina catalysts. The presence of an active cobalt-molybdate complex was concluded from magnetic susceptibility measurements. Moreover cobalt aluminate and cobalt oxide were found. Only the active cobalt molybdate complex would contribute to the activity and be characterized by octahedrally coordinated cobalt. Lipsch and Schuit (10) studied a commercial oxidic hydrodesulfurization catalyst, containing 12 wt% M0O3 and 4 wt% CoO. They concluded that a cobalt aluminate phase was present and could not find indications for an active cobalt molybdate complex. Recent magnetic susceptibility studies of the same type of catalyst (13) confirmed the conclusion of Lipsch and Schuit. 

In summary, fixed-bed processes have advantages in ease of scaleup and operation. The reactors operate in a downflow mode, with liquid feed trickling downward over the solid catalyst concurrent with the hydrogen gas. The usual catalyst is cobalt/molybdenum (Co/Mo) or nickel/molybdenum (Ni/Mo) on alumina (A1203) and contain 11-14% molybdenum and 2-3% of the promoter nickel or cobalt. The alumina typically has a pore volume of 0.5 ml/g. The catalyst is formed into pellets by extrusion, in shapes such as cylinders (ca. 2 mm diameter), lobed cylinders, or rings. 

The raw minerals mined from natural deposits comprise mixtures of different specific minerals. An early step in mineral processing is to use crushing and grinding to free these various minerals from each other. In addition, these same processes may be used to reduce the mineral particle sizes to make them suitable for a subsequent separation process. Non-ferrous metals such as copper, lead, zinc, nickel, cobalt, molybdenum, mercury, and antimony are typically produced from mineral ores containing these metals as sulfides (and sometimes as oxides, carbonates, or sulfates) [91,619,620], The respective metal sulfides are usually separated from the raw ores by flotation. Flotation processes are also used to concentrate non-metallic minerals used in other industries, such as calcium fluoride, barium sulfate, sodium and potassium chlorides, sulfur, coal, phosphates, alumina, silicates, and clays [91,619,621], Other examples are listed in Table 10.2, including the recovery of ink in paper recycling (which is discussed in Section 12.5.2), the recovery of bitumen from oil sands (which is discussed further in Section 11.3.2), and the removal of particulates and bacteria in water and wastewater treatment (which is discussed further in Section 9.4). 

The catalyst used in the experiments was a commercial cobalt molybdenum supported on y-alumina (Procatalyse HR306). It contains 14 wt% of molybdenum oxide and 3 wt% of cobalt oxide and has a surface area of 210 m2/g. It was sulfided according to a standard laboratory procedure at 400 °C under a mixture of 15 vol.% of H2S in H2. In one experiment, the activity of... 

Authentic and synthetic solvent-refined coal filtrates were processed upflow in hydrogen over three different commercially available catalysts. Residual (>850°F bp) solvent-refined coal versions up to 46 wt % were observed under typical hydrotreating conditions on authentic filtrate over a cobalt-molybdenum (Co-Mo) catalyst. A synthetic filtrate comprised of creosote oil containing 52 wt % Tacoma solvent-refined coals was used for evaluating nickel-molybdenum and nickel-tungsten catalysts. Nickel-molybdenum on alumina catalyst converted more 850°F- - solvent-refined coals, consumed less hydrogen, and produced a better product distribution than nickel-tungsten on silica alumina. Net solvent make was observed from both catalysts on synthetic filtrate whereas a solvent loss was observed when authentic filtrate was hydroprocessed. Products were characterized by a number of analytical methods. 

In the steam-reforming process, any sulfur compounds present in the hydrocarbon feedstock have to be removed because the nickel-containing catalysts are sensitive to poisons. This is either achieved by hydrodesulfurization (see Hydrodesulfurization Hydrodenitrogenation), generally with a combination of cobalt-molybdenum and zinc oxide... 

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