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Ammonia synthesis production

At the same time, running in long periods, i.e. improvement of operating rate is also the efficient way of energy-saving of plant. The actual energy consumption in ammonia synthesis production can be calculated as following equation ... [Pg.790]

A more elaborate variation gives a generell amino acid synthesis. If the reaction between an aldehyde and cyanide is done in the presence of ammonia, the product is an a-amino-nitrile ... [Pg.44]

Urea is produced from liquid NH and gaseous CO2 at high, pressure and temperature both reactants are obtained from an ammonia-synthesis plant. The latter is a by-product stream, vented from the CO2 removal section of the ammonia-synthesis plant. The two feed components are deUvered to the high pressure urea reactor, usually at a mol ratio >2.5 1. Depending on the feed mol ratio, more or less carbamate is converted to urea and water per pass through the reactor. [Pg.299]

Ammonia from coal gasification has been used for fertilizer production at Sasol since the beginning of operations in 1955. In 1964 a dedicated coal-based ammonia synthesis plant was brought on stream. This plant has now been deactivated, and is being replaced with a new faciUty with three times the production capacity. Nitric acid is produced by oxidation and is converted with additional ammonia into ammonium nitrate fertilizers. The products are marketed either as a Hquid or in a soHd form known as Limestone Ammonium Nitrate. Also, two types of explosives are produced from ammonium nitrate. The first is a mixture of fuel oil and porous ammonium nitrate granules. The second type is produced by emulsifying small droplets of ammonium nitrate solution in oil. [Pg.168]

Resources for Nitrogen Fertilizers. The production of more than 95% of all nitrogen fertilizer begins with the synthesis of ammonia, thus it is the raw materials for ammonia synthesis that are of prime interest. Required feed to the synthesis process (synthesis gas) consists of an approximately 3 1 mixture (by volume) of hydrogen and nitrogen. [Pg.243]

The Texaco process was first utilized for the production of ammonia synthesis gas from natural gas and oxygen. It was later (1957) appHed to the partial oxidation of heavy fuel oils. This appHcation has had the widest use because it has made possible the production of ammonia and methanol synthesis gases, as well as pure hydrogen, at locations where the lighter hydrocarbons have been unavailable or expensive such as in Maine, Puerto Rico, Brazil, Norway, and Japan. [Pg.422]

High temperature steam reforming of natural gas accounts for 97% of the hydrogen used for ammonia synthesis in the United States. Hydrogen requirement for ammonia synthesis is about 336 m /t of ammonia produced for a typical 1000 t/d ammonia plant. The near-term demand for ammonia remains stagnant. Methanol production requires 560 m of hydrogen for each ton produced, based on a 2500-t/d methanol plant. Methanol demand is expected to increase in response to an increased use of the fuel—oxygenate methyl /-butyl ether (MTBE). [Pg.432]

Feedstock Purification Manufacture of Synthesis Gases Hydrogen, Ammonia, Methanol, product bulletin. United Catalysts, Inc., Louisville, Ky. [Pg.462]

Based on these developments, the foreseeable future sources of ammonia synthesis gas are expected to be mainly from steam reforming of natural gas, supplemented by associated gas from oil production, and hydrogen rich off-gases (especially from methanol plants). [Pg.345]

Shift Conversion. Carbon oxides deactivate the ammonia synthesis catalyst and must be removed prior to the synthesis loop. The exothermic water-gas shift reaction (eq. 23) provides a convenient mechanism to maximize hydrogen production while converting CO to the more easily removable CO2. A two-stage adiabatic reactor sequence is normally employed to maximize this conversion. The bulk of the CO is shifted to CO2 in a high... [Pg.348]

The performance of many metal-ion catalysts can be enhanced by doping with cesium compounds. This is a result both of the low ionization potential of cesium and its abiUty to stabilize high oxidation states of transition-metal oxo anions (50). Catalyst doping is one of the principal commercial uses of cesium. Cesium is a more powerflil oxidant than potassium, which it can replace. The amount of replacement is often a matter of economic benefit. Cesium-doped catalysts are used for the production of styrene monomer from ethyl benzene at metal oxide contacts or from toluene and methanol as Cs-exchanged zeofltes ethylene oxide ammonoxidation, acrolein (methacrolein) acryflc acid (methacrylic acid) methyl methacrylate monomer methanol phthahc anhydride anthraquinone various olefins chlorinations in low pressure ammonia synthesis and in the conversion of SO2 to SO in sulfuric acid production. [Pg.378]

By-product power does not give enough power to match the demand for many processes such as ammonia synthesis, and designs have historically incorporated condensing turbines for incremental power with heat rejection to cooling water. A more effective response is use of the gas turbine combined cycle shown by Figures 5c and 6c. [Pg.224]

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]

The production of ammonia is of historical interest because it represents the first important application of thermodynamics to an industrial process. Considering the synthesis reaction of ammonia from its elements, the calculated reaction heat (AH) and free energy change (AG) at room temperature are approximately -46 and -16.5 KJ/mol, respectively. Although the calculated equilibrium constant = 3.6 X 108 at room temperature is substantially high, no reaction occurs under these conditions, and the rate is practically zero. The ammonia synthesis reaction could be represented as follows ... [Pg.144]

C15-0007. State the relative rates for the consumption of starting materials and the formation of products for the ammonia synthesis. [Pg.1059]

Ammonia synthesis is the second largest chemical process, after the production of sulfuric acid (see also Chapter 1). It accounts for about 1 % of the total human-related energy consumption. Roughly 80 % of the ammonia produced is used for fertilizers (either as liquid ammonia or as more easily handled salts such as ammonium nitrate, ammonium phosphate, etc.) and, as such, ammonia synthesis is indispensable for our society. Other applications of ammonia are nitrogen-containing... [Pg.328]

Kinetics of Ammonia Synthesis on Re Crystal Surfaces. The kinetics of the ammonia synthesis reaction on Re were studied on the Re(ll50) surface which is composed of atoms having seven-fold coordination. The rate of production at 70 K and 20 atm. ... [Pg.157]


See other pages where Ammonia synthesis production is mentioned: [Pg.209]    [Pg.258]    [Pg.277]    [Pg.164]    [Pg.216]    [Pg.216]    [Pg.11]    [Pg.11]    [Pg.423]    [Pg.437]    [Pg.83]    [Pg.339]    [Pg.342]    [Pg.342]    [Pg.344]    [Pg.350]    [Pg.508]    [Pg.481]    [Pg.484]    [Pg.1120]    [Pg.258]    [Pg.38]    [Pg.112]    [Pg.112]    [Pg.285]    [Pg.23]    [Pg.264]    [Pg.293]    [Pg.326]    [Pg.338]    [Pg.155]    [Pg.149]   
See also in sourсe #XX -- [ Pg.426 , Pg.427 , Pg.428 , Pg.429 ]




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