RU98119957A - METHOD FOR PRODUCING SYNTHESIS GAS FROM REACTIVE GAS MIXTURE, METHOD FOR PRODUCING SECOND SYNTHESIS GAS, METHOD FOR PRODUCING CHEMICAL PRODUCT USING SYNTHESIS GAS AND USING USING GAS-USED - Google Patents
METHOD FOR PRODUCING SYNTHESIS GAS FROM REACTIVE GAS MIXTURE, METHOD FOR PRODUCING SECOND SYNTHESIS GAS, METHOD FOR PRODUCING CHEMICAL PRODUCT USING SYNTHESIS GAS AND USING USING GAS-USEDInfo
- Publication number
- RU98119957A RU98119957A RU98119957/12A RU98119957A RU98119957A RU 98119957 A RU98119957 A RU 98119957A RU 98119957/12 A RU98119957/12 A RU 98119957/12A RU 98119957 A RU98119957 A RU 98119957A RU 98119957 A RU98119957 A RU 98119957A
- Authority
- RU
- Russia
- Prior art keywords
- synthesis gas
- range
- gas
- temperature
- catalyst
- Prior art date
Links
- 230000015572 biosynthetic process Effects 0.000 title claims 27
- 238000003786 synthesis reaction Methods 0.000 title claims 27
- 239000000203 mixture Substances 0.000 title claims 13
- 238000004519 manufacturing process Methods 0.000 title claims 6
- 239000000126 substance Substances 0.000 title claims 6
- 239000007789 gas Substances 0.000 claims 34
- 238000000034 method Methods 0.000 claims 28
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims 22
- 239000011949 solid catalyst Substances 0.000 claims 11
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 claims 10
- 239000003054 catalyst Substances 0.000 claims 8
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 7
- 239000001301 oxygen Substances 0.000 claims 7
- 229910052760 oxygen Inorganic materials 0.000 claims 7
- 229910052799 carbon Inorganic materials 0.000 claims 6
- 230000003647 oxidation Effects 0.000 claims 6
- 238000007254 oxidation reaction Methods 0.000 claims 6
- 229910002092 carbon dioxide Inorganic materials 0.000 claims 5
- 239000001569 carbon dioxide Substances 0.000 claims 5
- 150000001450 anions Chemical class 0.000 claims 4
- 238000006243 chemical reaction Methods 0.000 claims 4
- 239000004927 clay Substances 0.000 claims 4
- 238000010304 firing Methods 0.000 claims 4
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 claims 3
- 239000011230 binding agent Substances 0.000 claims 3
- 229910002091 carbon monoxide Inorganic materials 0.000 claims 3
- 230000006835 compression Effects 0.000 claims 3
- 238000007906 compression Methods 0.000 claims 3
- 239000001257 hydrogen Substances 0.000 claims 3
- 229910052739 hydrogen Inorganic materials 0.000 claims 3
- 239000000654 additive Substances 0.000 claims 2
- 230000000996 additive effect Effects 0.000 claims 2
- 150000001339 alkali metal compounds Chemical class 0.000 claims 2
- 229910001579 aluminosilicate mineral Inorganic materials 0.000 claims 2
- 150000001875 compounds Chemical class 0.000 claims 2
- 150000002431 hydrogen Chemical class 0.000 claims 2
- 229910052500 inorganic mineral Inorganic materials 0.000 claims 2
- 239000011707 mineral Substances 0.000 claims 2
- 229920001296 polysiloxane Polymers 0.000 claims 2
- 229910021647 smectite Inorganic materials 0.000 claims 2
- 230000000087 stabilizing effect Effects 0.000 claims 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims 1
- 150000001341 alkaline earth metal compounds Chemical class 0.000 claims 1
- 150000001342 alkaline earth metals Chemical class 0.000 claims 1
- 229910000278 bentonite Inorganic materials 0.000 claims 1
- 239000000440 bentonite Substances 0.000 claims 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical group O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 claims 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 claims 1
- 229910052615 phyllosilicate Inorganic materials 0.000 claims 1
- 229910052761 rare earth metal Inorganic materials 0.000 claims 1
- 150000002909 rare earth metal compounds Chemical class 0.000 claims 1
- 150000002910 rare earth metals Chemical class 0.000 claims 1
- 239000012495 reaction gas Substances 0.000 claims 1
- 239000011541 reaction mixture Substances 0.000 claims 1
Claims (21)
Mex 2++Mey 3++(OH)2x+3y+2z(A2-)z·nH2O,
где Me2+ является по существу полностью Ni2+, Me3+ является по существу полностью Al3+ или по существу Al3+ и Cr3+, A2 является или единственным двухвалентным анионом или двумя одновалентными анионами, x/y находится между 1,5/1 и 4/1, z/(x+y) находится в диапазоне 0,05-0,2, и n/(x+y) находится в диапазоне 0,25-1,0,
с необожженной алюмино-силикатной минеральной глиной и, в то же самое время и/или впоследствии, но до обжига, по меньшей мере, с одной стабилизирующей добавкой для сокращения потерь силикон-содержащих разновидностей, содержащих соединение щелочноземельного и/или редкоземельного металла, и, необязательно, соединение щелочного металла, а затем обжиг полученной смеси и восстановление вещества катализатора для активации катализатора.1. A method of producing synthesis gas from a reaction gas mixture containing methane, oxygen and, optionally, steam and / or carbon dioxide, comprising partial oxidation of methane by bringing the reacting gas mixture at a temperature in the range of 100 - 950 ° C and at a pressure of up to 150 bar in contact with the first solid catalyst that initiates the reaction, and carrying out the reaction essentially under adiabatic conditions to produce synthesis gas, the catalyst being prepared by a method comprising uniformly mixing a Feitknecht compound having a common ph formula
Me x 2+ + Me y 3+ + (OH) 2x + 3y + 2z (A 2-) z · nH 2 O,
where Me 2+ is essentially completely Ni 2+ , Me 3+ is essentially completely Al 3+ or essentially Al 3+ and Cr 3+ , A 2 is either the only divalent anion or two monovalent anions, x / y is between 1.5 / 1 and 4/1, z / (x + y) is in the range of 0.05-0.2, and n / (x + y) is in the range of 0.25-1.0,
with unbaked aluminosilicate mineral clay and, at the same time and / or subsequently, but before firing, with at least one stabilizing additive to reduce the loss of silicone-containing varieties containing a compound of an alkaline earth and / or rare earth metal, and, optionally, an alkali metal compound, and then firing the resulting mixture and reducing the catalyst substance to activate the catalyst.
Mex 2+Mey 3+(OH)2x+3y+2z(A2-)z·nH2O,
где Me2+ является по существу полностью Ni2+, Me3+ является по существу полностью Al3+ или по существу Al3+ и Cr3+, A2- является единственным дивалентным анионом или двумя моновалентными анионами, x/y находится между 1,5/1 и 4/1, z/(x+y) находится в диапазоне 0,05-0,2 и n/(x+y) находится в диапазоне 0,25 - 1,0
с необожженной алюмино-силикатной минеральной глиной и в то же самое время и/или впоследствии, но до обжига, по меньшей мере с одной стабилизирующей добавкой для сокращения потери силиконсодержащих разновидностей, содержащих соединение щелочноземельного и/или редкоземельного металла и необязательно соединение щелочного металла и затем обжиг полученной смеси и восстановление вещества катализатора для активации катализатора, и затем в) производство второго синтез-газа использованием в качестве подаваемого газа первого синтез-газа, который содержит монооксид углерода, диоксид углерода, водород, пар и непрореагировавший метан и не подвергнут стадии сжатия после его получения, содержит добавление кислорода к первому синтез-газу и вызывает частичное окисление еще не прореагировавшего метана, пропуская реагирующую смесь первого синтез-газа и кислорода при температуре в пределах 600 - 900° С и при давлении в пределах 25 - 100 бар через твердый катализатор и проведение дальнейшего частичного окисления при по существу адиабатных условиях для получения второго синтез-газа при относительно высокой температуре и давления; при этом полученный второй синтез-газ не подвергают сжатию после его производства и перед реакцией получения химического продукта.20. A method of producing a chemical product using a second synthesis gas obtained by a) producing a first synthesis gas from a reacting gas mixture containing methane, oxygen and optionally steam and / or carbon dioxide, with a temperature of the obtained first synthesis gas within 700 - 100 ° C and a pressure in the range of 25 - 100 bar and includes the partial oxidation of methane by conducting a reacting gas mixture at a temperature in the range of 100 - 950 ° C and at a pressure of up to 150 bar in contact with the first solid catalyst that initiates the reaction, and conducting react ii substantially under adiabatic conditions to produce a first synthesis gas, wherein the catalyst is prepared by a method comprising mixing a uniform Feitknecht-compound having the general formula
Me x 2+ Me y 3+ (OH ) 2x + 3y + 2z (A 2-) z · nH 2 O,
where Me 2+ is essentially completely Ni 2+ , Me 3+ is essentially completely Al 3+ or essentially Al 3+ and Cr 3+ , A 2- is the only divalent anion or two monovalent anions, x / y is between 1.5 / 1 and 4/1, z / (x + y) is in the range of 0.05-0.2 and n / (x + y) is in the range of 0.25 - 1.0
with unbaked aluminosilicate mineral clay and at the same time and / or subsequently, but before firing, with at least one stabilizing additive to reduce the loss of silicone-containing species containing an alkaline earth and / or rare earth metal compound and optionally an alkali metal compound and then firing the resulting mixture and reducing the catalyst substance to activate the catalyst, and then c) producing a second synthesis gas using the first synthesis gas as a feed gas, The second one contains carbon monoxide, carbon dioxide, hydrogen, steam and unreacted methane and is not subjected to a compression stage after its production, contains the addition of oxygen to the first synthesis gas and causes partial oxidation of the unreacted methane, passing the reaction mixture of the first synthesis gas and oxygen at at temperatures between 600 and 900 ° C and at pressures between 25 and 100 bar through a solid catalyst and further partial oxidation under essentially adiabatic conditions to produce a second synthesis gas with respect to high temperature and pressure; however, the obtained second synthesis gas is not subjected to compression after its production and before the reaction to obtain a chemical product.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB9607231.9 | 1996-04-04 | ||
| GB9607231A GB2311790A (en) | 1996-04-04 | 1996-04-04 | Production of synthesis gas from hydrocarbonaceous feedstock |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| RU98119957A true RU98119957A (en) | 2000-09-20 |
| RU2161120C2 RU2161120C2 (en) | 2000-12-27 |
Family
ID=10791690
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| RU98119957/12A RU2161120C2 (en) | 1996-04-04 | 1997-04-01 | Method of production of gas-synthesis from reaction gaseous mixture, method of production of second gas-synthesis, method of synthesis of chemical substance using gas-synthesis and second gas-synthesis |
Country Status (11)
| Country | Link |
|---|---|
| EP (1) | EP0891295A1 (en) |
| JP (1) | JP2000508286A (en) |
| AR (1) | AR006538A1 (en) |
| AU (1) | AU713494B2 (en) |
| CA (1) | CA2250893A1 (en) |
| GB (1) | GB2311790A (en) |
| ID (1) | ID17322A (en) |
| RU (1) | RU2161120C2 (en) |
| TN (1) | TNSN97062A1 (en) |
| WO (1) | WO1997037930A1 (en) |
| ZA (1) | ZA972890B (en) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5939353A (en) * | 1992-12-21 | 1999-08-17 | Bp Amoco Corporation | Method for preparing and using nickel catalysts |
| AU777809B2 (en) * | 2000-03-02 | 2004-11-04 | Boc Group, Inc., The | Catalytic monolith made of ceria and titania |
| NO316440B1 (en) † | 2000-05-18 | 2004-01-26 | Statoil Asa | Hydrotalcite-based material with improved strength, use and process thereof, and catalyst comprising this material |
| EP1188713A3 (en) * | 2000-09-18 | 2003-06-25 | Haldor Topsoe A/S | Production of hydrogen and carbon monoxide containing synthesis gas by partial oxidation |
| DE10055818A1 (en) * | 2000-11-10 | 2002-05-23 | Ammonia Casale Sa | Catalytic production of ammonia, especially for direct conversion into urea, using nitrogen-hydrogen starting gas mixture obtained from natural gas by autothermal reforming and catalytic conversion |
| FR2820416B1 (en) * | 2001-02-07 | 2003-12-05 | Cie D Etudes Des Technologies | PROCESS AND DEVICE FOR THE PRODUCTION OF HYDROGEN BY PARTIAL OXIDATION OF HYDROCARBON FUELS |
| GB0127517D0 (en) * | 2001-11-16 | 2002-01-09 | Statoil Asa | Catalysts |
| US6818198B2 (en) * | 2002-09-23 | 2004-11-16 | Kellogg Brown & Root, Inc. | Hydrogen enrichment scheme for autothermal reforming |
| US7427388B2 (en) | 2004-03-19 | 2008-09-23 | Air Products And Chemicals, Inc. | Process for improving prereforming and reforming of natural gas containing higher hydrocarbons along with methane |
| US7510793B2 (en) | 2004-08-05 | 2009-03-31 | Rolls-Royce Fuel Cell Systems (Us) Inc. | Post-reformer treatment of reformate gas |
| JP4838526B2 (en) * | 2005-03-31 | 2011-12-14 | 大阪瓦斯株式会社 | Syngas production method and apparatus |
| JP4781704B2 (en) * | 2005-03-31 | 2011-09-28 | 大阪瓦斯株式会社 | Method and apparatus for producing hydrogen-containing gas |
| RU2318722C2 (en) * | 2006-04-10 | 2008-03-10 | Федеральное государственное учреждение Российский научный центр "Курчатовский институт" | Plasma converter used for transformation of the gaseous and liquid hydrocarbon raw and the fuels into the synthesis gas on the basis of the microwave discharge |
| JP4886416B2 (en) * | 2006-08-04 | 2012-02-29 | 株式会社東芝 | Carbon monoxide reduction device, carbon monoxide reduction method, hydrogen production device, and fuel cell power generation system |
| JP5009109B2 (en) * | 2007-09-13 | 2012-08-22 | 関西電力株式会社 | Hydrocarbon partial oxidation catalyst and method and apparatus for producing hydrogen-containing gas using the same |
| JP5324265B2 (en) * | 2009-03-11 | 2013-10-23 | 関西電力株式会社 | Hydrocarbon partial oxidation catalyst and method and apparatus for producing hydrogen-containing gas using the same |
| JP7417920B2 (en) * | 2019-09-19 | 2024-01-19 | 国立大学法人北海道大学 | Light hydrocarbon partial oxidation catalyst and method for producing carbon monoxide and hydrogen using the catalyst |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4337170A (en) * | 1980-01-23 | 1982-06-29 | Union Carbide Corporation | Catalytic steam reforming of hydrocarbons |
| EP0303438A3 (en) * | 1987-08-14 | 1989-12-27 | DAVY McKEE CORPORATION | Production of synthesis gas from hydrocarbonaceous feedstock |
| JP2818171B2 (en) * | 1988-09-09 | 1998-10-30 | 東洋シーシーアイ株式会社 | Catalyst for steam reforming reaction of hydrocarbon and method for producing the same |
| GB2222963B (en) * | 1988-09-23 | 1992-01-02 | British Gas Plc | Catalysts |
| US5399537A (en) * | 1992-12-21 | 1995-03-21 | Amoco Corporation | Method for preparing synthesis gas using nickel catalysts |
| IT1256227B (en) * | 1992-12-23 | 1995-11-29 | Snam Progetti | CATALYTIC PROCEDURE FOR THE PRODUCTION OF SYNTHESIS GAS |
-
1996
- 1996-04-04 GB GB9607231A patent/GB2311790A/en not_active Withdrawn
-
1997
- 1997-04-01 JP JP9535945A patent/JP2000508286A/en active Pending
- 1997-04-01 WO PCT/GB1997/000900 patent/WO1997037930A1/en not_active Ceased
- 1997-04-01 CA CA002250893A patent/CA2250893A1/en not_active Abandoned
- 1997-04-01 AU AU22991/97A patent/AU713494B2/en not_active Ceased
- 1997-04-01 EP EP97915555A patent/EP0891295A1/en not_active Ceased
- 1997-04-01 RU RU98119957/12A patent/RU2161120C2/en not_active IP Right Cessation
- 1997-04-02 TN TNTNSN97062A patent/TNSN97062A1/en unknown
- 1997-04-04 ID IDP971139A patent/ID17322A/en unknown
- 1997-04-04 ZA ZA9702890A patent/ZA972890B/en unknown
- 1997-04-04 AR ARP970101358A patent/AR006538A1/en active IP Right Grant
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