Abstract: The present invention relates to a method for contemporaneously recovering ammonia and carbon dioxide from an aqueous solution thereof, possibly comprising their condensates, in a synthesis process of urea, characterized in that it comprises a hydrophobic microporous membrane distillation phase of an aqueous solution comprising ammonia, carbon dioxide and their saline compounds or condensates, said distillation being carried out at a temperature ranging from 50 to 250° C. and a pressure ranging from 50 KPa to 20 MPa absolute, with the formation of a residual aqueous solution, possibly comprising urea, and a gaseous permeate stream, comprising ammonia, carbon dioxide and water. The present invention also relates to an apparatus for effecting the above method and a production process of urea which comprises the above method.

Abstract: The present invention provides an amide compound having antibacterial activity, and a bacterial infection control agent for agricultural and horticultural use that contains the amide compound. The novel amide compound of the present invention is represented by General Formula (1): wherein R is a —CH(R1)(R2) or a —CO(R2) group, R1 is a hydrogen atom or a hydroxyl group, and R2 is a C1-12 alkyl group.

Abstract: A method for co-producing electric power and urea from carbonaceous fuels such as coal, by pyrolizing the coal with oxygen to produce a raw rich gas and a hot char which is gasified with air to produce a raw lean gas. Subsequent to the cleaning of the two gases, the cleaned rich gas is made up of CO and 2H2, and the clean lean gas is made up of N2+CO. The CO in the rich gas is separated from the 2H2 and is added to the lean gas to enrich it with CO to become a lean fuel gas which fuels a gas turbine and is part of a combined cycle system which efficiently generates electric power while exhausting an off-gas (flue gas) made up of N2+CO2. The 2H2 separated from the CO, and the N2+CO2 of the exhausted flue gas are together synthesized to produce urea —CO(NH2)2.

Abstract: Method for carbamate condensation of a carbon dioxide/ammonia gaseous phase in a liquid phase in a condensation unit of the so-called submerged type comprising a heat exchange tube bundle having a predetermined number of tubes intended for carbamate condensation, wherein the gaseous phase and the liquid phase are fed contemporaneously and independently to each of the tubes intended for condensation.

Abstract: Process for increasing the capacity of a urea plant comprising a compression section, a high-pressure synthesis section, a urea recovery section, in which a urea melt is formed, and optionally a granulation section, the capacity of the urea plant being increased by the additional installation of a melamine plant and the urea melt from the urea recovery section of the urea plant being fed wholly or partly to the melamine plant and the residual gases from the melamine plant being returned wholly or partly to the high-pressure synthesis section and/or the urea recovery section of the urea plant.

Abstract: Process for the combined preparation of urea and ammonia reactant by steps of providing ammonia synthesis gas containing carbon dioxide and conversion of the synthesis gas to the ammonia reactant, reacting the ammonia reactant with the carbon dioxide in the synthesis gas to ammonium carbamate and to urea product, which process comprises further steps of prior to the conversion of the synthesis gas to the ammonia reactant, (i) washing the synthesis gas with an aqueous solution of the ammonia reactant and forming a solution being rich in ammonium carbamate; (ii) removing excess of ammonia reactant from the washed synthesis gas by washing with water and withdrawing an aqueous solution of ammonia reactant; (iii) purifying the water washed synthesis gas by removing remaining amounts of water and ammonia; and (iv) passing the purified synthesis gas to the conversion of the gas to ammonia reactant.

Abstract: A plant for manufacturing urea from carbonaceous materials, oxygen from an air separation unit and water, preferably steam, is made up of a syngas generator unit, an air separation unit, Fischer-Tropsch unit, a CO2 removal unit, a hydrogen removal unit, a methanator unit, an ammonia converter unit and a urea synthesizer unit. Each of Fischer-Tropsch liquids, ammonia, hydrogen and urea can be recoverable under proper economic conditions. Electrical power is recoverable by the addition of at least one of a steam turbine and a gas turbine which is/are coupled to an electrical generator.

Abstract: The present invention is an integrated process for converting light hydrocarbon gas to heavier hydrocarbon liquids. In each embodiment, a Fischer-Tropsch (FT) process comprising a thermal reformer and a reactor containing an FT catalyst is combined with one or more additional processes to achieve operational synergies. In a first embodiment, an FT process is integrated with a cryogenic liquefied natural gas (LNG) process wherein tail gas from the FT reaction is used to drive a refrigeration compressor in the LNG process. The tail gas, optionally supplemented with natural gas, may be fed directly to a gas turbine or may be combusted in steam boiler, which in turn provides steam to a steam turbine. The natural gas may be processed prior to its being fed to the LNG process and the FT process in order to remove any impurities and/or condensate. The process may be further integrated with a fertilizer production process comprising an ammonia synthesis process and a urea synthesis process.

Abstract: Process for the preparation of urea, in which the gas stream which is released during the synthesis of melamine and is composed essentially of ammonia and carbon dioxide is used to synthesize urea, in which process the gas stream which originates from a high-pressure melamine process and is composed essentially of ammonia and carbon dioxide is condensed at a pressure virtually equal to the pressure in the melamine reactor, in which process substantially anhydrous ammonium carbamate is formed, after which said ammonium carbamate is fed to a high-pressure section of a urea stripping plant.

Abstract: In a process of producing urea in which ammonia and carbon dioxide are reacted in a first reaction space (E-1, R-1) the unreacted carbamate present in the reaction mixture is subjected to a thermal decomposition treatment, so as to obtain ammonia and carbon dioxide which are sent to a second reaction space (R-2) in which they react with a solution of recycled carbamate coming from an urea recovery section (3). Advantageously, the regulation of the temperature and of the ammonia/carbon dioxide molar ratio in the second reaction space (R-2) is carried out by respectively regulating the temperature of the recycled carbamate solution and the temperature of the thermal decomposition treatment of the residual carbamate leaving the first reaction space (E-1, R-1).

Abstract: A process for the production of urea comprising the steps of reacting carbon dioxide and ammonia to form ammonium carbamate and subsequent decomposition of ammonium carbamate to form a reaction mixture comprising urea and water, wherein the reaction mixture is contacted with one side of a semi-permeable membrane, and a drying fluid capable of removing water and possibly other reaction products(s) from the reaction mixture is contacted with the other side of the semi-permeable membrane.

Abstract: Process for the catalytic synthesis of nitrogen-containing organic compounds, comprising the reaction of carbon monoxide with at least one amino compound in a reaction mixture containing a catalyst based on selenium and a substituted pyridine. The process is particularly suitable for the synthesis of ureas and of their polymers.

Abstract: In a urea synthesis process, the reaction product from the reaction vessel is flowed in series through high pressure, medium pressure and low pressure decomposing and stripping devices to decompose ammonium carbamate to NH.sub.3 gas, CO.sub.2 gas and water vapor, and to remove those gases and unreacted starting materials from the aqueous urea solution. CO.sub.2 gas is used as the stripping gas in the decomposing and stripping devices.

Abstract: Disclosed are after-treatment processes and apparatus for synthesis plants, particularly urea and ammonium nitrate plants, but applicable also to various other plants in which the synthesis reaction does not go to substantial completion. In such plants product is fed to an evaporator for concentration and then to a solidification stage. The vaporous overhead stream from the evaporator contains entrained synthesis product, one or more unreacted starting materials, and solvent (usually H.sub.2 O). It is condensed, and the condensate is brought into mass and heat exchange relationship with the vaporous overhead stream from the evaporator substantially without material transfer of solvent to the condensate stream. The condensate stream is thereby enriched in synthesis product, heat is added to it, and unreacted starting material is desorbed from it. The product-enriched condensate is delivered to the solidification stage for processing there.

Abstract: A process for the preparation of urea and its derivatives by reacting CO, NO, and a hydrogen source over a supported noble metal catalyst at atmospheric pressure is described. Preferably, stoichiometric amounts of reactory gases are used. Reaction temperatures are in the range of 75.degree. C. to 225.degree. C.