SU626111A1 - Method of producing olefinic hydrocarbons - Google Patents
Method of producing olefinic hydrocarbonsInfo
- Publication number
- SU626111A1 SU626111A1 SU762381385A SU2381385A SU626111A1 SU 626111 A1 SU626111 A1 SU 626111A1 SU 762381385 A SU762381385 A SU 762381385A SU 2381385 A SU2381385 A SU 2381385A SU 626111 A1 SU626111 A1 SU 626111A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- weight
- raw materials
- iron
- raw material
- catalyst
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 20
- 229930195733 hydrocarbon Natural products 0.000 title claims description 8
- 150000002430 hydrocarbons Chemical class 0.000 title claims description 8
- 239000002994 raw material Substances 0.000 claims description 24
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 claims description 16
- 239000003054 catalyst Substances 0.000 claims description 16
- 150000001336 alkenes Chemical class 0.000 claims description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 6
- 239000004215 Carbon black (E152) Substances 0.000 claims description 4
- WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 claims description 4
- 229910000423 chromium oxide Inorganic materials 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 150000004945 aromatic hydrocarbons Chemical class 0.000 claims description 2
- 238000000197 pyrolysis Methods 0.000 claims description 2
- 230000009466 transformation Effects 0.000 claims description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims 6
- 239000005977 Ethylene Substances 0.000 claims 6
- 238000006243 chemical reaction Methods 0.000 claims 6
- 238000010790 dilution Methods 0.000 claims 6
- 239000012895 dilution Substances 0.000 claims 6
- 125000003118 aryl group Chemical group 0.000 claims 5
- UPHIPHFJVNKLMR-UHFFFAOYSA-N chromium iron Chemical compound [Cr].[Fe] UPHIPHFJVNKLMR-UHFFFAOYSA-N 0.000 claims 3
- 238000002474 experimental method Methods 0.000 claims 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims 2
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims 2
- QEFDIAQGSDRHQW-UHFFFAOYSA-N [O-2].[Cr+3].[Fe+2] Chemical group [O-2].[Cr+3].[Fe+2] QEFDIAQGSDRHQW-UHFFFAOYSA-N 0.000 claims 1
- NJFMNPFATSYWHB-UHFFFAOYSA-N ac1l9hgr Chemical compound [Fe].[Fe] NJFMNPFATSYWHB-UHFFFAOYSA-N 0.000 claims 1
- UOUJSJZBMCDAEU-UHFFFAOYSA-N chromium(3+);oxygen(2-) Chemical class [O-2].[O-2].[O-2].[Cr+3].[Cr+3] UOUJSJZBMCDAEU-UHFFFAOYSA-N 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 claims 1
- 229910052742 iron Inorganic materials 0.000 claims 1
- 239000000463 material Substances 0.000 claims 1
- DYPHJEMAXTWPFB-UHFFFAOYSA-N [K].[Fe] Chemical compound [K].[Fe] DYPHJEMAXTWPFB-UHFFFAOYSA-N 0.000 description 1
- IOUCSUBTZWXKTA-UHFFFAOYSA-N dipotassium;dioxido(oxo)tin Chemical compound [K+].[K+].[O-][Sn]([O-])=O IOUCSUBTZWXKTA-UHFFFAOYSA-N 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
Landscapes
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Изобретение относитс к нефтехимии, конкретно к области получени олефиновых углеводородов.The invention relates to petrochemistry, specifically to the field of olefinic hydrocarbon production.
Известен способ получени олефиновых углеводородов пиролизом углеводородного сырь в присутствии вод ного пара и катализатора - станната кали 1.A method of producing olefinic hydrocarbons is known by pyrolysis of a hydrocarbon feedstock in the presence of water vapor and a catalyst, potassium stannate 1.
Недостатком известного способа вл етс относительно невысокий выход целевых продуктов ( 60 %).The disadvantage of this method is the relatively low yield of the target products (60%).
Более близким к предложенному по сущности и достигаемому результату вл етс способ получени олефинов с использованием железохромкалиевого катализатора 2.Closer to the essentially proposed and achieved result is a method for producing olefins using an iron-potassium catalyst 2.
Данный способ позвол ет получать олефинов до 70 вес. %.This method allows olefins to be produced up to 70 wt. %
Недостатком известного способа вл етс невозможность получени значительных количеств олефинов без рециркул ции части сырь .The disadvantage of this method is the impossibility of obtaining significant quantities of olefins without recycling a part of the feedstock.
Цель предлагаемого изобретени - повышение выхода олефиновых углеводородов .The purpose of the present invention is to increase the yield of olefinic hydrocarbons.
Поставленна цель достигаетс за счет того, что используют катализатор, содержащий 7,0-20 вес. % окиси хрома и 80- 93 вес. % окиси железа.This goal is achieved due to the use of a catalyst containing 7.0-20 wt. % chromium oxide and 80-93 weight. % iron oxide.
Исследовани , проведенные в услови х опытных установок, позволили исключить недостатки известного способа, сохранив его преимущество.The studies carried out under the conditions of the pilot plants, made it possible to eliminate the disadvantages of this method, while retaining its advantage.
Высокий выход олефинов сохран етс . Катализатор в процессе длительной эксплуатации не требует регенерации и обладает хорошей механической прочностью. Возможно проведение процесса с полнымA high yield of olefins is maintained. The catalyst during long-term operation does not require regeneration and has good mechanical strength. It is possible to conduct the process with complete
превращением сырь .the transformation of raw materials.
Исследовани осуществл ют на укруппенной опытной установке в реакторе соThe studies were carried out on a group pilot plant in a reactor with
стационарным слоем катализатора (5 кг),fixed bed catalyst (5 kg),
наход щегос в изотермических услови хfound in isothermal conditions
(внешний обогрев). В качестве исходного сырь берут газовый бензин с н. к. 38°С и к. к. 160°С, содержащий до 80 вес. % углеводородов СБ. Концентраци ароматических углеводородов не превышает 1 %(external heating). As a feedstock take gas gasoline with n. to. 38 ° C and to. to. 160 ° C, containing up to 80 weight. % hydrocarbon sat. The concentration of aromatic hydrocarbons does not exceed 1%
(0,8 вес. %).(0.8 wt.%).
Claims (4)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SU762381385A SU626111A1 (en) | 1976-07-01 | 1976-07-01 | Method of producing olefinic hydrocarbons |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SU762381385A SU626111A1 (en) | 1976-07-01 | 1976-07-01 | Method of producing olefinic hydrocarbons |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU626111A1 true SU626111A1 (en) | 1978-09-30 |
Family
ID=20668903
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU762381385A SU626111A1 (en) | 1976-07-01 | 1976-07-01 | Method of producing olefinic hydrocarbons |
Country Status (1)
| Country | Link |
|---|---|
| SU (1) | SU626111A1 (en) |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4579997A (en) * | 1985-07-25 | 1986-04-01 | Phillips Petroleum Company | Olefin production over catalytic oxides of Mn and at least one of Nb and a lanthanide |
| US4613722A (en) * | 1985-07-25 | 1986-09-23 | Phillips Petroleum Company | Dehydrogenation of C3 and C4 hydrocarbons over an iron-based catalyst |
| US4620052A (en) * | 1985-07-25 | 1986-10-28 | Phillips Petroleum Company | Dehydrogenation and cracking of C3 and C4 hydrocarbons |
| US4620051A (en) * | 1985-07-25 | 1986-10-28 | Philips Petroleum Company | Dehydrogenation and cracking of C3 and C4 hydrocarbons to less saturated hydrocarbons |
| US4621163A (en) * | 1985-07-25 | 1986-11-04 | Phillips Petroleum Company | Conversion of C3 and C4 hydrocarbons to less saturated hydrocarbons |
| US4621162A (en) * | 1985-07-25 | 1986-11-04 | Phillips Petroleum Company | Method for conversion of C3 and C4 hydrocarbons to olefinic products |
| US4658081A (en) * | 1985-07-25 | 1987-04-14 | Phillips Petroleum Company | Propylene and ethylene selectivity with H2 S |
| RU2142495C1 (en) * | 1999-01-12 | 1999-12-10 | Московская государственная академия тонкой химической технологии им. М.В.Ломоносова | Lower olefins production process |
-
1976
- 1976-07-01 SU SU762381385A patent/SU626111A1/en active
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4579997A (en) * | 1985-07-25 | 1986-04-01 | Phillips Petroleum Company | Olefin production over catalytic oxides of Mn and at least one of Nb and a lanthanide |
| US4613722A (en) * | 1985-07-25 | 1986-09-23 | Phillips Petroleum Company | Dehydrogenation of C3 and C4 hydrocarbons over an iron-based catalyst |
| US4620052A (en) * | 1985-07-25 | 1986-10-28 | Phillips Petroleum Company | Dehydrogenation and cracking of C3 and C4 hydrocarbons |
| US4620051A (en) * | 1985-07-25 | 1986-10-28 | Philips Petroleum Company | Dehydrogenation and cracking of C3 and C4 hydrocarbons to less saturated hydrocarbons |
| US4621163A (en) * | 1985-07-25 | 1986-11-04 | Phillips Petroleum Company | Conversion of C3 and C4 hydrocarbons to less saturated hydrocarbons |
| US4621162A (en) * | 1985-07-25 | 1986-11-04 | Phillips Petroleum Company | Method for conversion of C3 and C4 hydrocarbons to olefinic products |
| US4658081A (en) * | 1985-07-25 | 1987-04-14 | Phillips Petroleum Company | Propylene and ethylene selectivity with H2 S |
| US4829041A (en) * | 1985-07-25 | 1989-05-09 | Phillips Petroleum Company | Composition of matter and method for conversion of C3 and C4 hydrocarbons |
| RU2142495C1 (en) * | 1999-01-12 | 1999-12-10 | Московская государственная академия тонкой химической технологии им. М.В.Ломоносова | Lower olefins production process |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Chang et al. | Process studies on the conversion of methanol to gasoline | |
| CA1156265A (en) | Process for carrying out catalytic conversions | |
| TWI629255B (en) | Process for converting paraffin to olefin and catalyst for use therein | |
| US3781195A (en) | Process for the production of gaseous olefins from petroleum distillate feedstocks | |
| CA1249847A (en) | Method for dehydrogenating hydrocarbons | |
| JPS61167629A (en) | Dehydrogenation isomerization of hydrocarbon | |
| GB878035A (en) | Improvements in or relating to the catalytic isomerization of olefinic hydrocarbons | |
| SU626111A1 (en) | Method of producing olefinic hydrocarbons | |
| Ezinkwo et al. | Overview of the Catalytic Production of Isoprene from different raw materials; Prospects of Isoprene production from bio-ethanol. | |
| US2565395A (en) | Production of hydrogen from hydrocarbon gases | |
| US4052477A (en) | Method for upgrading a fischer-tropsch light oil | |
| BR112021014626A2 (en) | METHOD TO PRODUCE LIQUEFIED PETROLEUM GAS | |
| Inui et al. | Selective conversion of propane into aromatics on platinum ion-exchanged gallium-silicate bifunctional catalysts | |
| US3751514A (en) | Preparation of isobutylene and propylene from isobutane | |
| US2422671A (en) | Process for lowering the molecular weight of nonaromatic hydrocarbons | |
| AU601642B2 (en) | Catalyst composition and method for conversion of c3 and c4 hydrocarbons | |
| JPS6263529A (en) | Selective production of ethylene and propylene | |
| SU850011A3 (en) | Method of preparing olefins | |
| US3321545A (en) | Olefins by hydrogen transfer | |
| US4021500A (en) | Oxidative dehydrogenation system | |
| US3267170A (en) | Process for forming olefins by hydrogen transfer | |
| US4066712A (en) | Reforming process using chromium trioxide-graphite intercalation catalyst | |
| TW201247596A (en) | Variations on prins-like chemistry to produce 2,5-dimethylhexadiene from isobutanol | |
| US4774376A (en) | Production of liquid products from aliphatic hydrocarbons | |
| US2865842A (en) | Cracking of a hydrocarbon oil with a silica-alumina-tungsten phosphate catalyst composite |