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Iron catalysts ammonia synthesis

Either H2 or CO and their mixtures can be used as reductant for F-T synthesis iron catalysts, while only H2 can be used as reductant for ammonia synthesis iron catalysts. It is the reason that the active phase for the former is iron carbide and the latter is metal iron after reduction. [Pg.387]

The concentration effect of poisons. There exists a range of concentration of poison that can make the catalyst inactive. This range varies with different catalysts, the chemical reactions involved and the reaction conditions. For instance, a 0.63% of sulfur adsorbed on an industrial ammonia synthesis iron catalyst will completely deactivate the catalyst. A typical cmve of the activity associated with the concentration of poison on an iron catalyst is shown in Fig. 8.24. Even if the concentration of poisons is very low, the activity of catalyst decreases linearly with the increase of the content of poisons. [Pg.693]

Relevant to the synthesis of ammonia over iron catalysts is the observation of Ertl et al. (54) that potassium preadsorbed by an iron catalyst ((7 = 0.1) increased the rate of synthesis at 430 K by a factor of about 300. This effect the authors attributed to an enhancement of the heat of adsorption of molecular nitrogen due to transfer of electronic charge from potassium to the surface of the iron catalyst. This would be entirely in keeping with the precursor model proposed for nitrogen chemisorption (55). [Pg.74]

It is known that the conditions of the reduction are important to the behavior of ammonia type iron catalysts during the synthesis of hydro-... [Pg.315]

In the case of the ammonia synthesis, iron nitrides instead of carbides were identified. in spent catalysts (Fe4N, Fe3N, and Fe2N). [Pg.316]

Potassium alum anhydrous Sodium alum catalyst, ammonia synthesis Iron Osmium... [Pg.4939]

Bare S R, Strongin D R and Somoqai G A 1986 Ammonia synthesis over iron single crystal catalysts—the effects of alumina and potassium J. Phys. Chem. 90 4726... [Pg.955]

In 1974 a 1000 t/d ammonia plant went into operation near Johaimesburg, South Africa. The lignitic (subbituminous) coal used there contains about 14% ash, 36% volatile matter, and 1% sulfur. The plant has six Koppers-Totzek low pressure, high temperature gasifiers. Refrigerated methanol (—38° C, 3.0 MPa (30 atm)) is used to remove H2S. A 58% CO mixture reacts with steam over an iron catalyst to produce H2. The carbon dioxide is removed with methanol (at —58° C and 5.2 MPa (51 atm)). Ammonia synthesis is carried out at ca 22 MPa (220 atm) (53) (see Ammonia). [Pg.160]

Reforming is completed in a secondary reformer, where air is added both to elevate the temperature by partial combustion of the gas stream and to produce the 3 1 H2 N2 ratio downstream of the shift converter as is required for ammonia synthesis. The water gas shift converter then produces more H2 from carbon monoxide and water. A low temperature shift process using a zinc—chromium—copper oxide catalyst has replaced the earlier iron oxide-catalyzed high temperature system. The majority of the CO2 is then removed. [Pg.83]

Recent commercialization efforts have focused on improved activity synthesis catalysts, which allow ammonia synthesis to be conducted at significantly lower pressures and temperatures. Catalyst manufacturers have focused on enhancing the activity of the iron-based catalyst through the use of promoters (23). [Pg.340]

The industrial catalysts for ammonia synthesis consist of far more than the catalyticaHy active iron (74). There are textural promoters, alumina and calcium oxide, that minimise sintering of the iron and a chemical promoter, potassium (about 1 wt % of the catalyst), and possibly present as K2O the potassium is beheved to be present on the iron surface and to donate electrons to the iron, increasing its activity for the dissociative adsorption of N2. The primary iron particles are about 30 nm in size, and the surface area is about 15 m /g. These catalysts last for years. [Pg.177]

Ammonia Synthesis. Ammonia (qv) has been manufactured by the hydrogenolysis of the N-N bond in nitrogen over an iron-based catalyst since the beginning of the twentieth century (46) ... [Pg.197]

Ammonia production from natural gas includes the following processes desulfurization of the feedstock primary and secondary reforming carbon monoxide shift conversion and removal of carbon dioxide, which can be used for urea manufacture methanation and ammonia synthesis. Catalysts used in the process may include cobalt, molybdenum, nickel, iron oxide/chromium oxide, copper oxide/zinc oxide, and iron. [Pg.64]

For the synthesis of ammonia, Nj -i- 3H2 —> 2NH3, over an iron catalyst, develop the rate expression for the following mechanism... [Pg.213]

The compressed synthesis gas is dried, mixed with a recycle stream, and introduced into the synthesis reactor after the recycle compressor. The gas mixture is chilled and liquid ammonia is removed from the secondary separator. The vapor is heated and passed into the ammonia converter. The feed is preheated inside the converter prior to entering the catalyst bed. The reaction occurs at 450-600°C over an iron oxide catalyst. The ammonia synthesis reaction between nitrogen, N2, and hydrogen, Hj, is... [Pg.1127]

Remaining trace quantities of CO (which would poison the iron catalyst during ammonia synthesis) are converted back to CH4 by passing the damp gas from the scmbbers over a Ni methanation catalyst at 325° CO -t- 3H2, CRt -t- H2O. This reaction is the reverse of that occurring in the primary steam reformer. The synthesis gas now emerging has the approximate composition H2 74.3%, N2 24.7%, CH4 0.8%, Ar 0.3%, CO 1 -2ppm. It is compressed in three stages from 25 atm to 200 atm and then passed over a promoted iron catalyst at 380-450°C ... [Pg.421]

The effect of alkali additives on N2 chemisorption has important implications for ammonia synthesis on iron, where alkali promoters (in the form of K or K20) are used in order to increase the activity of the iron catalyst. [Pg.50]

C.G. Yiokari, G.E. Pitselis, D.G. Polydoros, A.D. Katsaounis, and C.G. Vayenas, High pressure electrochemical promotion of ammonia synthesis over an industrial iron catalyst, /. Phys. Chem. 104, 10600-10602 (2000). [Pg.187]

The reactant is adsorbed on the catalyst s surface. As a reactant molecule attaches to the surface of the catalyst, its bonds are weakened and the reaction can proceed more quickly because the bonds are more easily broken (Fig. 13.36). One important step in the reaction mechanism of the Haber process for the synthesis of ammonia is the adsorption of N2 molecules on the iron catalyst and the weakening of the strong N=N triple bond. [Pg.687]

Mossbauer spectroscopy is a specialist characterization tool in catalysis. Nevertheless, it has yielded essential information on a number of important catalysts, such as the iron catalyst for ammonia and Fischer-Tropsch synthesis, as well as the CoMoS hydrotreating catalyst. Mossbauer spectroscopy provides the oxidation state, the internal magnetic field, and the lattice symmetry of a limited number of elements such as iron, cobalt, tin, iridium, ruthenium, antimony, platinum and gold, and can be applied in situ. [Pg.147]

Figure 7.22. NH3 concentration as a function of reactor length in the synthesis of ammonia with a potassium-promoted iron catalyst. The exit concentration is 19 % and corresponds to... Figure 7.22. NH3 concentration as a function of reactor length in the synthesis of ammonia with a potassium-promoted iron catalyst. The exit concentration is 19 % and corresponds to...
Oxygen-containing molecules cannot be tolerated in the ammonia synthesis, primarily because they form iron oxide that blocks the active surface. First the CO2 is removed, through a scrubber, by reaction with a strong base. The remaining CO (and CO2) is then removed by the methanation reaction, converting the CO into methane and water. Finally the water is removed by, for example, molecular sieves. Methane does not present problems because it interacts weakly with the catalyst surface. The gas mixture (Tab. 8.6) is compressed to the roughly 200 bar needed for ammonia synthesis and admitted to the reactor. [Pg.330]

Silvery, shiny, and hard. Unique metal, gives off an odor as it forms volatile 0s04 on the surface (oxidation states 81). Osmium is the densest element (22.6 g cm3 record ). Was replaced in filaments (Osram) by the cheaper tungsten. Used in platinum alloys and as a catalyst. Haber s first catalyst in ammonia synthesis was osmium, which fortunately could be replaced by doped iron. The addition of as little as 1 to 2 % of this expensive metal increases the strength of steel (e.g. fountain-pen tips, early gramophone needles, syringe needles). [Pg.73]

As catalysis proceeds at the surface, a catalyst should preferably consist of small particles with a high fraction of surface atoms. This is often achieved by dispersing particles on porous supports such as silica, alumina, titania or carbon (see Fig. 1.2). Unsupported catalysts are also in use. The iron catalysts for ammonia synthesis and CO hydrogenation (the Fischer-Tropsch synthesis) or the mixed metal oxide catalysts for production of acrylonitrile from propylene and ammonia form examples. [Pg.17]


See other pages where Iron catalysts ammonia synthesis is mentioned: [Pg.3034]    [Pg.3033]    [Pg.215]    [Pg.259]    [Pg.3034]    [Pg.3033]    [Pg.215]    [Pg.259]    [Pg.84]    [Pg.164]    [Pg.216]    [Pg.437]    [Pg.84]    [Pg.339]    [Pg.525]    [Pg.173]    [Pg.137]    [Pg.34]    [Pg.198]    [Pg.328]    [Pg.338]    [Pg.103]    [Pg.201]    [Pg.86]    [Pg.137]    [Pg.214]   
See also in sourсe #XX -- [ Pg.168 ]




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