Patent classifications
C01C1/0488
USE OF RENEWABLE ENERGY IN OLEFIN SYNTHESIS
An olefin synthesis plant comprising: a feed pretreatment section configured to pretreat a feed stream; a pyrolysis section comprising one or more pyrolysis reactors configured to crack hydrocarbons in the feed stream in the presence of a diluent to produce a cracked gas stream; a primary fractionation and compression section configured to provide heat recovery from and quenching of the cracked gas stream; remove a component from the cracked gas stream; and compress the cracked gas stream, thus providing a compressed cracked gas stream; and/or a product separation section configured to separate a product olefin stream from the compressed cracked gas stream, wherein the olefin synthesis plant is configured such that, relative to a conventional olefin synthesis plant, more of the energy and/or the net energy required by the olefin synthesis plant and/or one or more sections thereof, is provided by a non-carbon based and/or renewable energy source and/or electricity.
USE OF INTERMITTENT ENERGY IN THE PRODUCTION OF CHEMICALS
A chemical synthesis plant comprising: one or more reactors configured for producing, from one or more reactants, a process stream comprising at least one chemical product; a feed preparation system configured to prepare one or more feed streams comprising one or more of the one or more reactants for introduction into the reactor; and/or a product purification system configured to separate the at least one chemical product from reaction byproducts, unreacted reactants, or a combination thereof within the process stream, wherein the chemical synthesis plant is configured such that a majority (e.g., greater than 50, 60, 70, 80, 90, or 100%) of the net energy needed for heating, cooling, compressing, or a combination thereof utilized via the one or more reactors, the feed preparation system, the product purification system, or a combination thereof is provided from an intermittent energy source (IES).
USE OF RENEWABLE ENERGY IN AMMONIA SYNTHESIS
An ammonia synthesis plant comprising: a feed pretreating section operable to pretreat a feed stream; a syngas generation section operable to reform the feed stream to produce a reformer product stream; a shift conversion section operable to subject the reformer product stream to the water gas shift reaction, to produce a shifted gas stream comprising more hydrogen than the reformer gas stream; a purification section operable to remove at least one component from the shifted gas stream, and provide an ammonia synthesis feed stream; and/or an ammonia synthesis section operable to produce ammonia from the ammonia synthesis feed stream, wherein the ammonia synthesis plant is configured such that, relative to a conventional ammonia synthesis plant, more of the energy required by the ammonia synthesis plant or one or more sections thereof is provided by a non-carbon based energy source, a renewable energy source, and/or electricity.
Steam network assembly for a plant comprising an ammonia-producing unit and a urea-producing unit
A steam network assembly for a plant including an ammonia-producing unit and a urea-producing unit, including a high-pressure steam line, two medium-pressure steam lines and first and second turbines supplied with high-pressure steam by the high-pressure steam line; wherein the first turbine is a condensing-type turbine with extraction into one of the two medium-pressure steam lines, and is configured to deliver power to a syngas compressor in the ammonia-producing unit of the plant, and the second turbine is a counter-pressure type turbine with extraction connected to the two medium-pressure steam lines and is configured to deliver power to a CO.sub.2 compressor in the urea-producing unit of the plant. A method to distribute high-pressure steam in a steam network assembly for a plant including an ammonia-producing unit and a urea-producing unit and a method to revamp the steam network assembly for a plant including an ammonia-producing unit and a urea-producing unit.
Process for nitric acid production
Integrated process for the synthesis of ammonia and nitric acid, comprising a synthesis of nitric acid including the following steps: a) subjecting a stream of ammonia (10) to catalytic oxidation, obtaining a gaseous stream containing nitrogen oxides (13); b) subjecting said gaseous stream to a process of absorption of nitrogen oxides, providing nitric acid (16) and a tail gas (17) containing nitrogen and residual nitrogen oxides; c) subjecting at least a portion of said first tail gas (17) to a process of removal of nitrogen oxides, providing a nitrogen oxides-depleted tail gas (18), and comprising a synthesis of ammonia by catalytic conversion of a make-up gas (126, 226) comprising hydrogen and nitrogen in an ammonia synthesis loop, wherein at least a portion (18b, 18d, 21) of said second tail gas is used as nitrogen source for obtaining said make-up gas (126, 226).
Co-production of methanol and ammonia
Process for the co-production of methanol and ammonia from a hydrocarbon feed without venting to the atmosphere carbon dioxide captured from the methanol or ammonia synthesis gas and without using expensive air separation units and water gas shift.
Production of carbon dioxide and ammonia from residual gases in the steel and metal industries
The present invention relates to a process for the production of carbon dioxide and ammonia for the production of urea or ammonium carbamate from residual gases in the steel and metal industries, in particular basic oxygen furnace (BOF) gas and/or blast furnace (BF) gas. The process according to the invention comprises: (a) subjecting a mixture comprising (i) basic oxygen furnace gas and/or blast furnace gas and (ii) steam to a separation-enhanced water gas shift reaction to obtain a first product gas comprising H.sub.2 and N.sub.2 and a second product gas comprising CO.sub.2; (b) subjecting the first product gas originating from step (a) to NH.sub.3 synthesis to obtain a product gas comprising NH.sub.3; and (c) optionally subjecting at least part of the CO.sub.2 originating from step (a) and at least part of the NH.sub.3 originating from step (b) to the synthesis of urea or ammonium carbamate.
Co-production of methanol, ammonia and urea
Process for the co-production of methanol and ammonia together with urea production from a hydrocarbon feed without venting to the atmosphere carbon dioxide captured from the methanol or ammonia synthesis gas and without using expensive air separation units and water gas shift. Carbon dioxide removal from flue gas from reforming section to convert partially or fully all ammonia into urea. Synergi of having methanol, ammonia and urea production to produce coating material for the urea production.
METHOD FOR AVOIDING VOC AND HAP EMISSIONS FROM SYNTHESIS GAS-PROCESSING SYSTEMS
Systems and methods for the synthesis of ammonia includes a reformer; a carbon monoxide converter; a carbon dioxide scrubber unit with recovery; a methanation unit; and an ammonia synthesis unit; wherein the carbon dioxide scrubber unit with recovery is connected to at least one fired auxiliary steam boiler.
Ammonia process using advanced shift process
A process for producing an ammonia synthesis gas, said process comprising the steps of: —Reforming a hydrocarbon feed in a reforming step thereby obtaining a synthesis gas comprising CH.sub.4, CO, CO.sub.2, H.sub.2 and H.sub.2O, —Shifting the synthesis gas in one in or more shift steps in series, —Optionally wash the synthesis gas leaving the shift section with water, —Sending the process condensate originating from cooling and washing the synthesis gas leaving the shift section to a process condensate stripper wherein the dissolved shift byproducts and dissolved gases are stripped out of the process condensate using steam resulting in a steam stream containing more than 99% of the dissolved methanol in process condensate. —Adding all or part of said steam stream from the process condensate stripper to the synthesis gas downstream the reforming step, prior to the last shift step, wherein —The steam/carbon ratio in the reforming step and the shift step is less than 2.6.