WO1991006504A1 - Method for obtaining nitrogen-hydrogen gas mixture for production of ammonia - Google Patents

Method for obtaining nitrogen-hydrogen gas mixture for production of ammonia Download PDF

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Publication number
WO1991006504A1
WO1991006504A1 PCT/SU1990/000196 SU9000196W WO9106504A1 WO 1991006504 A1 WO1991006504 A1 WO 1991006504A1 SU 9000196 W SU9000196 W SU 9000196W WO 9106504 A1 WO9106504 A1 WO 9106504A1
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WO
WIPO (PCT)
Prior art keywords
mixture
pressure
nitrogen
production
carbon dioxide
Prior art date
Application number
PCT/SU1990/000196
Other languages
English (en)
French (fr)
Russian (ru)
Inventor
Mikhail Khaimovich Sosna
July Kivovich Baichtok
Aleftina Leonidovna Lobanovskaya
Marina Petrovna Shilkina
Vladimir Zalmanovich Mordkovich
Original Assignee
Gosudarstvenny Nauchno-Issledovatelsky I Proektny Institut Azotnoi Promyshlennosti I Produktov Organicheskogo Sinteza
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from SU894754591A external-priority patent/SU1770277A1/ru
Priority claimed from SU4767286 external-priority patent/RU2022927C1/ru
Application filed by Gosudarstvenny Nauchno-Issledovatelsky I Proektny Institut Azotnoi Promyshlennosti I Produktov Organicheskogo Sinteza filed Critical Gosudarstvenny Nauchno-Issledovatelsky I Proektny Institut Azotnoi Promyshlennosti I Produktov Organicheskogo Sinteza
Publication of WO1991006504A1 publication Critical patent/WO1991006504A1/ru

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Classifications

    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B3/00Hydrogen; Gaseous mixtures containing hydrogen; Separation of hydrogen from mixtures containing it; Purification of hydrogen
    • C01B3/02Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen
    • C01B3/025Preparation or purification of gas mixtures for ammonia synthesis

Definitions

  • Received by this synthesis gas has a relationship ⁇ is ⁇ di ⁇ znachi ⁇ elny ⁇ as ⁇ ⁇ d uglev ⁇ d ⁇ dn ⁇ g ⁇ sy ⁇ ya and ene ⁇ gii, ⁇ me ⁇ g ⁇ ⁇ e ⁇ vichnaya ⁇ nve ⁇ siya ⁇ susches ⁇ vlyae ⁇ sya ⁇ zhes ⁇ - ⁇ i ⁇ ⁇ ezhimsh ⁇ usl ⁇ viya ⁇ .
  • the 5th year of the inversion is 820- ⁇ 050 ° ⁇ ; medium- and low-temperature conversion of carbon dioxide with the formation of carbon dioxide, which is based on catalysts at temperature of -90 ° C; Calculation of invert gas from carbon dioxide; Calculation of invert gas
  • the 30 required volume of the inverted gas is indispensable to be separated, for the purpose of producing a continuous system for the synthesis of ammonia, which is associated with significant energy.
  • Izves ⁇ en s ⁇ s ⁇ b ⁇ lucheniya ⁇ d ⁇ ds ⁇ de ⁇ zhascheg ⁇ gas ( ⁇ , ⁇ , 106076) v ⁇ lyuchayuschy mixing uglev ⁇ d ⁇ dn ⁇ g ⁇ sy ⁇ ya with ⁇ a ⁇ m, ⁇ azdelenie ⁇ bscheg ⁇ ⁇ a two chas ⁇ i, ⁇ dnu of ⁇ y ⁇ ⁇ dve ⁇ gayu ⁇ ⁇ e ⁇ vichn ⁇ y ⁇ a ⁇ v ⁇ y ⁇ a ⁇ ali ⁇ iches ⁇ y ⁇ n- ⁇ e ⁇ sii and ⁇ dayu ⁇ on v ⁇ ichnuyu ⁇ a ⁇ uyu ⁇ a ⁇ ali ⁇ iches ⁇ uyu ⁇ n- ve ⁇ siyu with v ⁇ zdu ⁇ m, ⁇ uda It gives off and the second part of the original steam and carbon.
  • the process of primary conversion is carried out with the production of indirect gas (nitrogen-by-product mixture) at the outlet, which is supplied with a by-product, - 4 - This is the first part of the general heating of the original hydrocarbon mixture at the stage of the steam in general.
  • the method also includes a medium- and low-temperature conversion of carbon monoxide, which is contained in the resulting nitrogen—
  • the aforementioned method is associated with a significant waste of energy at the stage of low separation of the radiation and upon receipt of an aqueous mixture of a commercial system. 20
  • the energy reserve is 0.77 GJ in.
  • P ⁇ i presence ⁇ s ⁇ eme ⁇ DYA ⁇ ⁇ a ⁇ a, 15 na ⁇ dyascheg ⁇ sya ⁇ d pressure ⁇ a ⁇ Ym or ⁇ e ⁇ Yshayuschim pressure is ⁇ dn ⁇ y az ⁇ v ⁇ d ⁇ dn ⁇ y mixture tseles ⁇ b ⁇ azn ⁇ , s ⁇ glasn ⁇ ⁇ edlagaem ⁇ mu iz ⁇ b ⁇ e ⁇ eniyu, selection of ⁇ d ⁇ da az ⁇ v ⁇ d ⁇ dn ⁇ y ⁇ susches ⁇ vlya ⁇ mixture ⁇ m ⁇ schyu di ⁇ uzi ⁇ nny ⁇ elemen ⁇ v.
  • the claimed s ⁇ s ⁇ b ⁇ ednaznachen for is ⁇ lz ⁇ aniya in ⁇ aches ⁇ ve is ⁇ dn ⁇ g ⁇ sy ⁇ ya ⁇ a ⁇ g ⁇ uglev ⁇ d ⁇ dn ⁇ g ⁇ sy ⁇ ya, ⁇ a ⁇ , na ⁇ ig ⁇ e ⁇ , me ⁇ an, e ⁇ an, and ⁇ an i ⁇ mixture vys ⁇ sche uglev ⁇ d ⁇ dy, na ⁇ dyaschiesya ⁇ i n ⁇ malny ⁇ usl ⁇ viya ⁇ 35 gaz ⁇ b ⁇ azn ⁇ m or zhid ⁇ m s ⁇ s ⁇ yanii.
  • the specified coal raw materials are mixed in comparison with that, it complies with - 6 -
  • the resulting gas mixture after mixing, is heated to a temperature of 450 ° C and the vapor pressure is increased; 5 Pa ⁇ vaya ⁇ nve ⁇ siya e ⁇ m in case ⁇ susches ⁇ vlyae ⁇ sya in s ⁇ ve ⁇ s ⁇ II with end ⁇ e ⁇ miches ⁇ y ⁇ ea ⁇ tsiey ⁇ i is ⁇ lz ⁇ va- Vania, na ⁇ ime ⁇ , ni ⁇ elev ⁇ g ⁇ ⁇ a ⁇ aliza ⁇ a, ⁇ ea ⁇ tsi ⁇ nnyi gas ⁇ em ⁇ e ⁇ a ⁇ u ⁇ y 621-749 C ⁇ dve ⁇ gayu ⁇ v ⁇ ichn ⁇ y ⁇ a ⁇ - v ⁇ y ⁇ a ⁇ ali ⁇ iches ⁇ y ⁇ nve ⁇ sii, ⁇ susches ⁇ vlyaem ⁇ y in ⁇ isu ⁇ s ⁇ - Yu Wii v ⁇ zdu ⁇ a, ⁇ y imee ⁇ not ⁇ eshe ⁇ a
  • the resulting nitric mixture is cooled to a temperature of 360 ° C and is supported by a steam converter in the mixture of carbon monoxide.
  • the developed carbon dioxide separates the nitrogen mixture from any known mixture, such as, for example, absorbs.
  • Sustainable carbon dioxide (0.5%) is suitable for metallurgical treatment at a temperature of 200-400 ° ⁇ .
  • the pressure is 5 bar, -
  • the allocation of household equipment exists through 35 interconnections, for example, Sha. 5 , Geh, Gehn, or diffusion through metallic membranes, for example, through palladium-containing membranes.
  • the remaining after separation of the water in quantities of up to 92 wt.
  • the poor mixture is divided - 7 - in two ways, one of the outputs is derived from the technical scheme (with the subsequent use of its energy), and the other is mixed with other
  • a variant of the implementation of the method is the separation of the nitrogen mixture and the solution, which does not increase
  • the natural hydrocarbon gas of the following composition ⁇ 4 - .82,2; C 2 ⁇ 6 - 4.47 total ; - 1.36% vol .; C 4 ⁇ ⁇ 0 -
  • the resulting ammonia mixture is sold at a temperature of 360 ° 0 and is fed to the steam converter for the conversion of carbon dioxide to a concentration of 16.0%.
  • Carbon dioxide 25 and carbon dioxide are removed from the nitrogen mixture until the residual content of mixtures in the mixture is no more than 5 ppm.
  • the natural hydrocarbon gas of the following composition 0 ⁇ 4 - 82.11% w, 0 2 ⁇ 3 - 4.47% w. , 0 ⁇ 8 - 1.36% by volume, ⁇ 4 ⁇ ⁇ 0 - 0.48%. , ⁇ 5 ⁇ ⁇ 2 - 0.24 ob. , ⁇ 0 2 - 0.03% by weight, ⁇ 2 - 4.20% by weight; and - 7.07 ob. ; ⁇ g - 0.03% by weight with a pressure of 4.3 ⁇ Pa is mixed with water in steam: carbon, equal to 2.52: 1, heats up to a temperature of 450 ° C and is supplied A quick output of the reactive mixture with temperature 729, ° ⁇ .
  • the content of ⁇ 4 in dry gas is 27.80% by volume.
  • the inverted gas after the stage of the upstream steam supply, transfers the stage of the upstream gas to the inverter.
  • a heated mixture with a temperature of Verizontage ⁇ 0 / inlet ⁇ 0.1 is also supplied here with a preheated temperature of 700 ° 0.
  • the resulting nitrous mixture is cooled at a temperature of 360 ° C and fed to the steam converter for the conversion of carbon dioxide to a total of about 82%.
  • Carbon dioxide and carbon dioxide are removed from the nitrogen mixture to the residual content of mixtures in the mixture no more than 5 ppm.
  • the purified nitrous mixture of the following composition: ⁇ 2 - 62.02% by volume, ⁇ 2 - 36.55% by weight, ⁇ g - 0.44%. , ⁇ - 0.99% by pressure 2.99 ⁇ Pa is divided into two flows in relation to 0.55: 0.45.
  • the natural hydrocarbon gas is as follows: 0 ⁇ - 32.36% w, 0 2 ⁇ 6 - 4.49% w, 0 3 ⁇ 8 - 1.37% w,
  • the nitrogenous mixture is fed to the stage of the primary conversion, where it is cooled
  • Carbon dioxide and carbon monoxide are separated from the nitrogenous mixture until the remaining mixture in the mixture is more than 5 ppm.
  • - II Of the purified aqueous mixture of the following system ⁇ 2 - 64.67% w, ⁇ - 33.79% w, ⁇ g - 0.40%. , 0 ⁇ 4 - 1.17 With a pressure of 2.99 Sha, with diffused palladium-containing membranes in the presence of a steam, which is kept at a temperature of 90, it is I am condensing, using it and this thermal conduction in the process flow.
  • synthesis gas is produced for the production of ammonia of the following composition: ⁇ 2 - 74.09%,, 2 - 24.73%. , ⁇ g - 0.29 , ⁇ 4 - 0.84% of the total commercially available nitrogen, equal to 3.
  • the nitrogenous mixture is fed to the stage of the primary conversion, where it is cooled - 12 - a temperature of 580 ° 0 is given, giving heat to the endothermic steam methane inversion, which flows to this stage.
  • the resulting nitrous mixture is cooled at a temperature of 5 ° 360 ° 0 and fed to the steam inversion of carbon dioxide for the conversion of carbon dioxide to a concentration of at least 22%.
  • Carbon dioxide and carbon dioxide are separated from the nitrogen mixture to the residual content of mixtures in the mixture not more than 10 ⁇ Jr.
  • the water is discharged at a pressure of 30.0 PSa.
  • the following composition was ⁇ 2 - 14.99%, ⁇ 2 - - 81.49%, ⁇ g - 0.97%, 0 ⁇ 4 - 2.55%. %% and temperature 20 ° C minus ⁇ 80 ° 0 separates excess nitrogen with amounts of - 2 - 1.13%. , ⁇ d - 2.51% by volume, 0 ⁇ 4 - 7.18% by weight with a pressure of 0.7 ⁇ Pa and get out of the process system using its energy.
  • Non-organic nitrogen which is in the nitrogen mixture, having a composition of 2 - 77.25% by weight, 25 ⁇ 2 -22.6%% by weight, _g _ 0.13% by weight, 0 ⁇ - 0.01% by weight, mix selected ⁇ d ⁇ d ⁇ m, ⁇ luchaya ⁇ i e ⁇ m az ⁇ v ⁇ d ⁇ dnuyu gaz ⁇ vuyu mixture ⁇ izv ⁇ ds ⁇ va ammia ⁇ a sleduyuscheg ⁇ s ⁇ s ⁇ a- wa:. ⁇ 2 - ⁇ b 74.96%, ⁇ 2 _ ⁇ b 24.989%, ⁇ g - 0.04 ⁇ b%, 0 ⁇ 4 - 0.007 ⁇ b.. . With a commercially available water content of 30% nitrogen, equal to 3.
PCT/SU1990/000196 1989-10-30 1990-07-31 Method for obtaining nitrogen-hydrogen gas mixture for production of ammonia WO1991006504A1 (en)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
SU4754591/23 1989-10-30
SU894754591A SU1770277A1 (ru) 1989-10-30 1989-10-30 Способ производства аммиака
SU4767286/26 1989-12-20
SU4767286 RU2022927C1 (ru) 1989-12-20 1989-12-20 Способ производства аммиака

Publications (1)

Publication Number Publication Date
WO1991006504A1 true WO1991006504A1 (en) 1991-05-16

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Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/SU1990/000196 WO1991006504A1 (en) 1989-10-30 1990-07-31 Method for obtaining nitrogen-hydrogen gas mixture for production of ammonia

Country Status (5)

Country Link
JP (1) JPH04503659A (ja)
DE (1) DE4092058T (ja)
FR (1) FR2671338A1 (ja)
GB (1) GB2244484B (ja)
WO (1) WO1991006504A1 (ja)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2065337A1 (en) * 2007-11-27 2009-06-03 Ammonia Casale S.A. Process for producing ammonia synthesis gas

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3206514A1 (de) * 1982-02-24 1983-09-01 Didier Engineering Gmbh, 4300 Essen Verfahren zur erzeugung von ammoniak-synthesegas
DE3335087A1 (de) * 1983-09-28 1985-04-11 Didier Engineering Gmbh, 4300 Essen Verfahren zur erzeugung von ammoniak-synthesegas
US4725380A (en) * 1984-03-02 1988-02-16 Imperial Chemical Industries Plc Producing ammonia synthesis gas
SU1527155A1 (ru) * 1987-08-24 1989-12-07 Государственный научно-исследовательский и проектный институт азотной промышленности и продуктов органического синтеза Способ синтеза аммиака

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA1229485A (en) * 1984-01-23 1987-11-24 Toyo Engineering Corporation Process for refining an ammonia synthesis gas
FR2614612B1 (fr) * 1987-04-28 1990-09-14 Technip Cie Procede de production amelioree de gaz d'ammoniac et installation pour l'execution de ce procede
JPH029701A (ja) * 1988-06-27 1990-01-12 Japan Metals & Chem Co Ltd 水素の精製方法

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3206514A1 (de) * 1982-02-24 1983-09-01 Didier Engineering Gmbh, 4300 Essen Verfahren zur erzeugung von ammoniak-synthesegas
DE3335087A1 (de) * 1983-09-28 1985-04-11 Didier Engineering Gmbh, 4300 Essen Verfahren zur erzeugung von ammoniak-synthesegas
US4725380A (en) * 1984-03-02 1988-02-16 Imperial Chemical Industries Plc Producing ammonia synthesis gas
SU1527155A1 (ru) * 1987-08-24 1989-12-07 Государственный научно-исследовательский и проектный институт азотной промышленности и продуктов органического синтеза Способ синтеза аммиака

Also Published As

Publication number Publication date
GB2244484A (en) 1991-12-04
GB9112665D0 (en) 1991-07-31
DE4092058T (ja) 1991-11-21
JPH04503659A (ja) 1992-07-02
FR2671338A1 (fr) 1992-07-10
GB2244484B (en) 1993-09-08

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