WO1996013331A1 - Catalyseur de conversion d'hydrocarbure et procede de conversion catalytique avec ce catalyseur - Google Patents
Catalyseur de conversion d'hydrocarbure et procede de conversion catalytique avec ce catalyseur Download PDFInfo
- Publication number
- WO1996013331A1 WO1996013331A1 PCT/JP1995/002040 JP9502040W WO9613331A1 WO 1996013331 A1 WO1996013331 A1 WO 1996013331A1 JP 9502040 W JP9502040 W JP 9502040W WO 9613331 A1 WO9613331 A1 WO 9613331A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- catalyst
- zeolite
- zsm
- hydrocarbon conversion
- type
- Prior art date
Links
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J29/00—Catalysts comprising molecular sieves
- B01J29/04—Catalysts comprising molecular sieves having base-exchange properties, e.g. crystalline zeolites
- B01J29/06—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof
- B01J29/40—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of the pentasil type, e.g. types ZSM-5, ZSM-8 or ZSM-11, as exemplified by patent documents US3702886, GB1334243 and US3709979, respectively
- B01J29/42—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of the pentasil type, e.g. types ZSM-5, ZSM-8 or ZSM-11, as exemplified by patent documents US3702886, GB1334243 and US3709979, respectively containing iron group metals, noble metals or copper
- B01J29/46—Iron group metals or copper
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J29/00—Catalysts comprising molecular sieves
- B01J29/04—Catalysts comprising molecular sieves having base-exchange properties, e.g. crystalline zeolites
- B01J29/06—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof
- B01J29/40—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of the pentasil type, e.g. types ZSM-5, ZSM-8 or ZSM-11, as exemplified by patent documents US3702886, GB1334243 and US3709979, respectively
- B01J29/42—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of the pentasil type, e.g. types ZSM-5, ZSM-8 or ZSM-11, as exemplified by patent documents US3702886, GB1334243 and US3709979, respectively containing iron group metals, noble metals or copper
- B01J29/44—Noble metals
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J29/00—Catalysts comprising molecular sieves
- B01J29/04—Catalysts comprising molecular sieves having base-exchange properties, e.g. crystalline zeolites
- B01J29/06—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof
- B01J29/064—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof containing iron group metals, noble metals or copper
- B01J29/068—Noble metals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C4/00—Preparation of hydrocarbons from hydrocarbons containing a larger number of carbon atoms
- C07C4/02—Preparation of hydrocarbons from hydrocarbons containing a larger number of carbon atoms by cracking a single hydrocarbon or a mixture of individually defined hydrocarbons or a normally gaseous hydrocarbon fraction
- C07C4/06—Catalytic processes
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C5/00—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms
- C07C5/32—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by dehydrogenation with formation of free hydrogen
- C07C5/373—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by dehydrogenation with formation of free hydrogen with simultaneous isomerisation
- C07C5/393—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by dehydrogenation with formation of free hydrogen with simultaneous isomerisation with cyclisation to an aromatic six-membered ring, e.g. dehydrogenation of n-hexane to benzene
- C07C5/41—Catalytic processes
- C07C5/415—Catalytic processes with metals
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G11/00—Catalytic cracking, in the absence of hydrogen, of hydrocarbon oils
- C10G11/02—Catalytic cracking, in the absence of hydrogen, of hydrocarbon oils characterised by the catalyst used
- C10G11/04—Oxides
- C10G11/05—Crystalline alumino-silicates, e.g. molecular sieves
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G11/00—Catalytic cracking, in the absence of hydrogen, of hydrocarbon oils
- C10G11/14—Catalytic cracking, in the absence of hydrogen, of hydrocarbon oils with preheated moving solid catalysts
- C10G11/18—Catalytic cracking, in the absence of hydrogen, of hydrocarbon oils with preheated moving solid catalysts according to the "fluidised-bed" technique
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2529/00—Catalysts comprising molecular sieves
- C07C2529/04—Catalysts comprising molecular sieves having base-exchange properties, e.g. crystalline zeolites, pillared clays
- C07C2529/06—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof
- C07C2529/40—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of the pentasil type, e.g. types ZSM-5, ZSM-8 or ZSM-11
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G2400/00—Products obtained by processes covered by groups C10G9/00 - C10G69/14
- C10G2400/20—C2-C4 olefins
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G2400/00—Products obtained by processes covered by groups C10G9/00 - C10G69/14
- C10G2400/30—Aromatics
Definitions
- the present invention relates to a catalytic conversion catalyst for hydrocarbons and a catalytic conversion method. More specifically, catalysts for catalytically cracking hydrocarbon feedstocks and the use of these catalysts make it possible to use petrochemical feedstocks of low-grade olefins whose main components are ethylene, benzene, toluene, The present invention relates to a method for efficiently and stably producing a monocyclic aromatic hydrocarbon containing xylene as a main component.
- PCTZJP 95/0109 is used to produce aromatic hydrocarbons from light hydrocarbons using a specific zeolite-based catalyst in a catalyst bed having a specific temperature distribution. A method has been proposed.
- the present invention makes it possible to obtain a low-level olefin containing ethylene as a main component and a monocyclic aromatic hydrocarbon in a well-balanced and high yield, and furthermore, there is little deterioration due to high-temperature steam.
- a highly stable hydrocarbon conversion catalyst and a production method using the above catalyst.
- the present inventors have solved the above problems, and have developed one or more hydrocarbons. Efficient use of lower olefins and monocyclic aromatic hydrocarbons from raw materials containing nitrogen, and higher yield of lower olefins containing ethylene as the main component than monocyclic aromatic hydrocarbons We intensively studied how to obtain a high rate. As a result, the use of mesoporous zeolite catalysts containing lb group metals and containing substantially no protons surprisingly reduces the efficiency of lower olefins and monocyclic aromatic hydrocarbons. It has been found that a lower olefin having ethylene as a main component can be obtained more stably and in a higher yield than a monocyclic aromatic.
- the present invention is a S i 0 2 / A 1 2 0 3 molar ratio of 2 0 or more, one or have a metal belonging to two or more periodic table I b group, substantially flop port DOO
- An object of the present invention is to provide a hydrocarbon conversion catalyst comprising a mesoporous zeolite containing no carbon dioxide.
- the intermediate pore diameter zeolite in the present invention is a medium pore diameter of a small pore diameter zeolite represented by A-type zeolite, a large pore diameter zeolite represented by mordenite, X-type, and Y-type zeolite. And has an effective pore diameter in the range of about 5 A to about 6.5 A.
- Typical examples are ZSM-5, ZSM-8, ZSM-11, ZSM-12, ZSM-21, ZSM-23, ZSM-35, ZSM-38, etc. Strong and preferred are ZSM-5 zeolites, such as ZSM-5, ZSM-11, ZSM-8, and ZSM-38, with ZSM-5 being particularly preferred.
- the Si 0./A 1: ⁇ molar ratio of the zeolite of the present invention is determined by the catalyst Therefore, 20 or more is required for stability.
- the upper limit of S i 0 2 / A 1 2 0 3 molar ratio is not particularly limited, in general, S i ⁇ 2 / A 1 2 0 3 molar ratio of 2 0-5 0 0 about And preferably about 28 to 300 are used.
- the catalyst of the present invention requires that the mesoporous zeolite be substantially free of protons.
- the phrase "substantially free of protons” as used herein means that the amount of protons (acid amount) determined by liquid phase ion exchange-filtration method is 0.02 millimol or less per gram of the zeolite. , More preferably less than 0.01 millimol.
- the amount of protons (acid amount) determined by liquid phase ion exchange-filtration method is 0.02 millimol or less per gram of the zeolite. , More preferably less than 0.01 millimol.
- For the method for measuring the amount of acid by the liquid phase ion exchange filtration method see Intraze 0 lite Chemistry, "ACSS ymp. Ser. J, 2 18, P 36 9-38 2 (1 983, U.S.A.), Nikka Kagaku, [3], P. 5 2 1 — 5 2 7 (1 989).
- the liquid-phase ion-exchange-filtration method used in the present invention refers to a method in which 1.5 g of zeolite calcined at a temperature of 400 to 600 ° C. in air is converted to 3.4 mol Z liter. The mixture was subjected to ion exchange in 25 ml of an aqueous NaCl solution for 10 minutes under ice-cooling.After filtration, the zeolite was further washed with 50 ml of pure water, and the entire filtrate was recovered. A method in which neutralization titration is performed with a 0.1 N Na ⁇ H aqueous solution and the amount of zeolite proton is determined from the neutralization point.
- polyvalent metal cation type zeolites such as ammonium ion type and rare earth metal ion type generate protons by heat treatment. Therefore, when measuring the amount of protons, it is necessary to perform the measurement using the sample that has been subjected to the above-mentioned baking treatment.
- One preferred embodiment of the substantially proton-free zeolite of the present invention is an alkali metal ion and a Z or alkaline earth metal ion type zeolite. It is preferably of the alkali metal ion type, with Na and Z or K ion type intermediate pore size zeolites being particularly preferred. or Intermediate pore S zeolites containing both Na, Na and / or K ions and alkaline earth metal ions can also be suitably used.
- the method of converting the intermediate pore diameter zeolite into an alkaline metal ion and / or an alkaline earth metal ion type may be carried out by a known ion exchange method. It is important to perform sufficient ion exchange with alkali metal ions and / or alkaline earth metal ions until the zeolite is substantially free of acidic sites.
- Another preferred embodiment of the zeolite substantially free of protons of the present invention is heat treatment, preferably zeolite heat-treated in the presence of steam, or repetition of reaction-regeneration.
- This is a zeolite that has been pre-processed.
- the heat treatment is preferably carried out at a temperature of 500 ° C. or higher, more preferably at 500 ° C. (up to 900 ° C.)
- the water vapor treatment is preferably performed at a temperature of 500 ° C. It can be carried out at a temperature of 500 ° C. or higher, more preferably 500 ° C. to 900 ° C., and a water vapor partial pressure of 0.01 atm or more. Alternatively, it may be carried out before introducing two or more kinds of metals belonging to Group lb of the periodic table, but preferably after the introduction.
- metals belonging to Group Ib of the Periodic Table it is necessary to introduce one or more metals selected from metals belonging to Group Ib of the Periodic Table into the zeolite.
- metals belonging to the lb group of the periodic table copper and silver are preferred, and silver is particularly preferred.
- a method for introducing one or more metals belonging to the lb group of the periodic table there can be mentioned usual methods such as an ion exchange method, an impregnation method and a kneading method.
- the exchange method is particularly preferred.
- the introduced Group Ib metal may be present in the form of an oxide, but at least a part thereof is present as a cation in zeolite.
- Examples of the metal salt used include silver nitrate, silver acetate, silver sulfate, copper chloride, and sulfuric acid. Copper oxide, copper nitrate, gold chloride, and the like.
- the content of Group Ib metal relative to zeolite is preferably 0.110% by weight, more preferably 0.25% by weight. If the content of the lb group metal is less than 0.1% by weight, the activity is not sufficient, and if the content exceeds 10% by weight, the performance is not further improved.
- zeolite is converted to alkali metal ions and / or alkali metal ions. It may be an earth metal ion type. However, in any case, it is important to prepare zeolite after preparation so that it does not substantially have an acidic site.
- the zeolites can be used after firing if necessary.
- the firing temperature is usually 500 000 ° C.
- the porosity of refractory inorganic oxides such as aluminum, silica, silica, alumina, zirconia, titania, silicate, clay, etc.
- Substances can also be compounded as matrices or binders and molded.
- the raw material containing one or more hydrocarbons may be selected from the group consisting of noremal fin, isolafine, ore fin, and C 4 to C 25.
- Approximately 25 cycloparaffins, cycloparaffins having a side chain alkyl group, etc. are contained as a main component, for example, gases such as ethane, propane, butane, butene, etc.
- Light naphtha mainly composed of pentane, pentene, hexane, heptane, octane alone and mixtures thereof, heavy naphtha, straight run naphtha, kerosene gas oil fraction mainly containing C, C 1;, ⁇ C.
- Propane, butane, butene, pentane, pentene, and mixtures thereof, and the naphtha fraction are preferred.
- the above catalyst is used in a catalytic cracking reaction, that is, by bringing the above-mentioned hydrocarbon raw material into contact with the hydrocarbon conversion catalyst of the present invention at a high temperature, a lower olefin and a monocyclic aromatic compound are obtained. Can produce aromatic hydrocarbons.
- the conditions of the catalytic cracking reaction of the present invention differ depending on the hydrocarbon feedstock.
- the contact time between the hydrocarbon feed and the catalyst must be set in consideration of the thermal decomposition properties of the hydrocarbon feed and the reaction temperature so that the effect of ripening is not excessive, but is usually 1 second. The following are appropriate:
- the catalytic cracking reaction of the present invention may be of any type, such as a fixed bed type, a moving bed type, a fluidized bed type, or a pneumatic conveying type.
- a Quick Cntact (QC) type reaction mode can be suitably used.
- QC Quick Cntact
- the regeneration of the catalyst in the catalytic cracking reaction is usually carried out by burning off the coke on the catalyst at a temperature of 400 to 900 ° C in air or an inert gas containing oxygen. can do.
- a temperature of 400 to 900 ° C in air or an inert gas containing oxygen can do.
- the power required to supply a heat of reaction and a regeneration temperature higher than the reaction temperature is required.
- the catalyst of the present invention has high hydrothermal stability. Even in such high-temperature regeneration, catalyst deterioration is small and stable.
- the catalyst of the present invention is used for a catalytic cyclization reaction by adding a hydrogenated Z-dehydrogenation metal component to the above catalyst.
- zeolite's dehydrocyclization ability is improved, and It can be used as a suitable catalyst for producing a monocyclic aromatic hydrocarbon.
- Metals and their compounds belonging to groups Hb, ⁇ b and ⁇ b of the periodic table are preferably zinc, gallium, indium, nickel, palladium, platinum and their oxides, and composite oxides. More preferably, it is a composite oxide of zinc and zinc such as zinc oxide and zinc aluminate. It is preferable that the amount of the metal belonging to Group Db, IEb, or the cyclic of the periodic table and the compound thereof with respect to zeolite is 0.1 to 20% by weight in terms of the metal.
- the conditions of the catalytic cyclization reaction of the present invention are as follows: a hydrocarbon feedstock, in particular, a force that varies depending on the ratio of olefin and paraffin in the feedstock, at a temperature of 300 to 65 ° C., hydrocarbon partial pressure of atmospheric pressure to 3 0 atm, 0.. 1 to 5 0 hr one a weight hourly space velocity (WHSV) Dearuko and is rather preferred, Shi further favored the 4 0 0 to 6 0 0 ° C Temperature.
- WHSV weight hourly space velocity
- any of fixed-bed, moving-bed and fluidized-bed reactors can be applied, and the reaction mode is not particularly limited, but preferred is a simple structure.
- the regeneration of the catalyst in the catalytic cyclization reaction is usually carried out by burning off the catalyst on the catalyst at a temperature of 400 to 700 ° C in air or an inert gas containing oxygen. It can be implemented by
- the mixture was calcined at 550 in air to prepare Catalyst 1.
- the acid content of this catalyst determined by liquid phase ion exchange-filtrate titration was 0.004 mmol Zg.
- the composition was represented by the molar ratio of the oxide on an anhydrous basis and had the following composition.
- Example 1 A naphtha conversion reaction was carried out under the same conditions as in Example 1 except that the Na + type ZSM-5 obtained in Example 1 was used as a catalyst (comparative catalyst 1). The acid content of this catalyst was 0.006 mmol Zg. Conclusion The results are shown in Table 1.
- the composition was represented by the molar ratio of oxide on an anhydrous basis and had the following composition.
- Table 1 shows the results of the naphtha conversion reaction performed using Comparative Catalyst 2 under the same conditions as in Example 1.
- Example 1 As in Example 1, except that zeolite was replaced with a porcelain lashing ring (outer diameter 3 mm0, length 3 mm), the naphtha pyrolysis was performed at 680 ° C. It was carried out. The results are shown in Table 1.
- a Na + -type ZSM-5 zeolite catalyst containing copper was prepared in the same manner as in Example 1, except that a 0.1 N copper chloride aqueous solution was used instead of the 0.02 N silver nitrate aqueous solution.
- the acid content of this catalyst was 0.006 mmol.
- the composition was represented by the molar ratio of oxide on an anhydrous basis and had the following composition.
- Table 1 shows that Na'-type ZSM-5 zeolite shows almost no naphtha-decomposing activity. However, when silver or copper is introduced into the zeolite, the decomposition activity is dramatically improved, and the yield is further improved. structure differs significantly from a g H T-type ZSM 5 obtained by introducing silver or copper ZSM 5 acid form, remarkable selectivity of lower Orefu fin consisting mainly of E Ji Le emissions Power to improve c
- a Na-type ZSM-5 zeolite catalyst containing silver (catalyst 2) was prepared in the same manner as in Example 1 except that the concentration of the aqueous silver nitrate solution was changed to 0.1 N. In addition, the acid amount of this catalyst was 0.004 mmo1 / g. As a result of the chemical analysis, the composition was represented by the following molar ratio of oxides on an anhydrous basis.
- a naphtha conversion reaction was carried out in the same manner as in Example 3 except that the reaction temperature was changed to 680 ° C. Table 2 shows the results.
- a silver-containing ZSM-5 zeolite catalyst (Catalyst 3) was prepared in the same manner as in Example 1 except that sodium chloride was changed to potassium chloride and the concentration of the aqueous silver nitrate solution was changed to 0.1 N. ) was prepared. The acid amount of this catalyst was 0.02 mm0] / g. As a result of the chemical analysis, the composition was represented by the molar ratio of the oxide on an anhydrous basis and had the following composition.
- Example 1 was repeated except that the reaction temperature was changed to 660 ° C using catalyst 3. A naphtha conversion reaction was performed under the same conditions. The results are shown in Table 2.
- Example 6
- the naphtha conversion reaction was carried out under the same conditions as in Example 5, except that the catalyst charge was changed from 2 g to 3 g, and the reaction temperature was set at 680 ° C. Table 2 shows the results.
- the naphtha was thermally decomposed under the same conditions as in Comparative Example 3 except that the reaction temperature was set at 790 ° C. The results are shown in Table 2.
- Example 8 The quartz reaction tube used in Example 1 was charged with 2 g of the catalyst 4 and heated to a predetermined temperature under atmospheric pressure while flowing nitrogen at 100 cc Z min. After the flow of nitrogen was stopped in order to carry out the reaction under undiluted conditions, naphtha of the same raw material used in Example 2 was supplied to the reaction tube at 46.8 cc / hr. The reaction product was analyzed 6 minutes after the start of the naphtha supply. Table 3 shows the reaction results.
- Example 8 The quartz reaction tube used in Example 1 was charged with 2 g of the catalyst 4 and heated to a predetermined temperature under atmospheric pressure while flowing nitrogen at 100 cc Z min. After the flow of nitrogen was stopped in order to carry out the reaction under undiluted conditions, naphtha of the same raw material used in Example 2 was supplied to the reaction tube at 46.8 cc / hr. The reaction product was analyzed 6 minutes after the start of the naphtha supply. Table 3 shows the reaction results.
- Example 8
- the naphtha conversion reaction was carried out under the same conditions as in Example 7 except that the H + type ZSM-5 used in Comparative Example 2 was used as a catalyst and the amount of catalyst was 1 g. Table 3 shows the results.
- the Na + -type ZSM-5 zeolite used in Example 8 was ion-exchanged with a 1N aqueous nitric acid solution (10 g-zeolite) at room temperature for 3 hours to obtain an H + -type ZSM-5 zeolite. did. Subsequently, ion exchange was performed at room temperature for 3 hours in a 0.03 N silver nitrate aqueous solution (10 ml / g—zeolite) to prepare Comparative Catalyst 3. The acid content of this catalyst was 0.42 mm 01 / g. As a result of chemical analysis, the composition was represented by the following molar ratio of oxides on an anhydrous basis.
- Table 3 shows the results of the conversion reaction performed under the same conditions as in Example 1 except that the catalyst loading was changed to 1 g using Comparative Catalyst 3.
- a magnesium nitrate aqueous solution (10 mf / g — zeolite)
- ion exchange at 90 ° C for 2 hours wash with filtered water, dry at 110 ° C, and dry with Mg 2 + Na + type ZSM 5 was prepared.
- the Mg 2 + Na + type ZSM-5 was subjected to an ion exchange treatment at room temperature for 3 hours using a 0.1 N aqueous solution of silver nitrate (10 ml £ Z g -zeolite). After washing with water and drying, the mixture was calcined at 550 ° C.
- the composition was represented by the molar ratio of the oxide on an anhydrous basis and had the following composition.
- Silver-containing Ca 2 + Na + -type ZSM-5 zeolite was prepared in the same manner as in Example 9 except that magnesium nitrate was changed to calcium nitrate.
- the acid content of this catalyst was 0.3 mm 0 1 Z g.
- the composition was represented by the following molar ratio of oxides on an anhydrous basis.
- Table 4 shows the results of the naphtha conversion reaction performed under the same conditions as in Example 9 using this catalyst.
- a silver-containing Ba 2 + Na + -type ZSM-5 zeolite was prepared in the same manner as in Example 9, except that magnesium nitrate was changed to barium acetate.
- the acid amount of this catalyst was 0.002 mmol / g.
- the composition was expressed as the molar ratio of oxides on an anhydrous basis and It had a 1 G composition.
- Table 4 shows the results of the naphtha conversion reaction performed under the same conditions as in Example 9 using this catalyst.
- silver-containing Ba 2 + Na + -type ZSM-5 zeolite was prepared.
- the acid content of this catalyst was 0.002 mmol Zg.
- the composition was represented by the molar ratio of the oxide on an anhydrous basis and had the following composition.
- Table 4 shows the results of the naphtha conversion reaction performed under the same conditions as in Example 1 using this catalyst.
- Table 5 shows the results of the naphtha conversion reaction performed under the same conditions as in Example 1 using this catalyst.
- Example 14 A catalyst containing 1.3% by weight of silver was prepared in the same manner as in Example 13 except that the concentration of the aqueous silver nitrate solution was changed to 0.1 N. The steaming treatment was performed under the same conditions as in Example 13, and the acid amount of the treated catalyst was 0.013 mm.
- Table 5 shows the results of a naphtha conversion reaction performed under the same conditions as in Example 1 using this catalyst.
- Example 13 The zeolite used in Example 13 was used as a catalyst without performing the steaming treatment, and a naphtha conversion reaction was carried out under the same conditions as in Example 1. Table 5 shows the results.
- the acid content of this catalyst was 0.118 mmo 1 Zg.
- the conversion of naphtha was carried out under the same conditions as in Example 1, except that the zeolite used in Example 14 was not subjected to the steaming treatment and was used as a catalyst.
- Table 5 shows the results.
- the acid amount of this catalyst was 0.055 mmolZ: ,,.
- Example 15 The experiment was performed in the same manner as in Example 15 except that the H-type ZSM-5 zeolite used in Comparative Example 2 was used as a catalyst, the filling amount was 4 g, and the steaming time was 40 minutes. Was done. Table 6 shows the results.
- the activity of the acid-type zeolite used in Comparative Example 8 was significantly reduced in a short time when exposed to high-temperature steam, whereas the activity of the catalyst of the present invention was extremely reduced. Small and stable.
- the catalyst of the present invention has a much higher deterioration resistance than a catalyst containing an acid-type zeolite containing silver (Comparative Catalyst 2).
- a silver-containing Na—type ZSM-5 zeolite catalyst (catalyst 7) was prepared in the same manner as in Example 7, except that the concentration of the aqueous silver nitrate solution was changed to 0.1 N.
- the acid content of this catalyst was 0.002 mmo1 / g.
- the composition was represented by the following molar ratio of oxides on an anhydrous basis.
- the naphtha conversion reaction was performed for 6 minutes under the same conditions as in Example 1. I went there. Next, after the reaction gas remaining in the reaction tube was replaced with nitrogen at 100 cc Z min for 2 minutes, 100 cc / in of air was passed through for 10 minutes, and accumulated on the catalyst by the naphtha conversion reaction. The coke was burned off. Further, in order to replace air and gas generated by coke combustion, nitrogen was passed at 100 cc / min for 2 minutes. The cycle from the naphtha conversion reaction to the second nitrogen flow was defined as one cycle, and this was repeated for 264 cycles. Table 7 shows the results of the first and second cycles.
- a naphtha conversion reaction was carried out under the same conditions as in Example II except that 2.5 g of this catalyst was charged to the reactor and the sampling time was set to 4.5 minutes.
- Table 8 shows the results.
- the amount of acid per 1 g of zeolite of this catalyst was 0.050 mmo1 / g.
- the composition was represented by the molar ratio of the oxide on an anhydrous basis and had the following composition.
- the amount of acid in the zeolite of the catalyst was 0.005 mmol Zg.
- this catalyst was impregnated with a 3N aqueous solution of zinc nitrate (0.5 ml / g-zeolite) and calcined to obtain a zinc-containing ZSM-5 zeolite forming catalyst (catalyst 8).
- the composition was represented by the molar ratio of oxides on a water-free basis and had the following composition.
- the raw material hydrocarbons (0.1% by weight of propane, 0.2% by weight of propylene, 7.7% by weight of butanes, 32.0% by weight of butenes, 45.7% by weight of pentanes %, Pentenes 14.3% by weight) was supplied to the reaction tube at 280 g ZH r to carry out a hydrocarbon conversion reaction.
- Table 9 shows the reaction results 4 hours and 40 hours after the start of raw material supply.
- the method of the present invention can maintain high selectivity for a long time.
- the catalyst of the present invention shows high activity, and the catalyst deterioration due to high-temperature steam is suppressed to a small extent.
- the present invention it is possible to obtain a lower-order olefin containing ethylene as a main component and a monocyclic aromatic hydrocarbon in good balance and high yield, and at a high temperature.
- a stable hydrocarbon conversion catalyst with little deterioration due to steam is provided. Therefore, the present invention can be widely used in the petrochemical industry and petroleum refining, and is particularly effective for producing lower olefins such as ethylene and propylene, aromatic compounds, and high octane gasoline.
- Zeolite AgNa-type Na-type AgH-type Pyrolysis CuNa-type Acid amount (mmol / g) 0.004 0.006 0.055 0.006
- Hydrocarbon raw material Naphtha Naphtha Naphtha Naphtha Naphtha Naphtha Reaction temperature (.C) 6 8 0 6 8 0 6 8 0 6 8 0 6 8 0 Yield (% by weight)
- Example 3 Example 4 Example 5 Example 6 Comparative Example 4 Zeolato AgNa-type AgNa-type AgK-type AgK-type Pyrolytic acid amount (mmol / g) 0.004 0.004 0.002 0.002
- Example 18 Comparative Example 1 2 Amount of acid (mmol / g; 0.005 0.24 Reaction time (hr.)) 4 40 4 4 1 Reaction temperature (.C) 5 1 7 5 1 7 5 1 7 5 1 7 Reaction pressure (kg / cm 2 G) 5.0 5.0 5.0 5.0 5.0 5.0 WHS V (hr- ') 2.8 1 2.8 1 2.8 1 2.8 1 2.8 1 Yield (weight )
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Crystallography & Structural Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Materials Engineering (AREA)
- Catalysts (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Description
Claims
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP95933621A EP0788838B1 (en) | 1994-10-28 | 1995-10-05 | Method of catalytic hydrocarbon conversion with a silver zeolite catalyst |
DE69534721T DE69534721T2 (de) | 1994-10-28 | 1995-10-05 | Methode zur katalytischen umwandlung von kohlenwasserstoffen mittels eines silber-zeolith-katalysators |
RU97108555A RU2133639C1 (ru) | 1994-10-28 | 1995-10-05 | Катализатор для преобразования углеводородов и способ получения низших олефинов и моноциклических ароматических углеводородов |
US08/809,830 US5968342A (en) | 1994-10-28 | 1995-10-05 | Zeolite catalyst and method of converting hydrocarbons using the same |
KR1019970702809A KR100233194B1 (ko) | 1994-10-28 | 1995-10-05 | 탄화수소 전화 촉매 및 그것을 사용하는 접촉 전화 방법 |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6/264996 | 1994-10-28 | ||
JP26499694A JP3664502B2 (ja) | 1994-10-28 | 1994-10-28 | 低級オレフィン及び単環芳香族炭化水素の製造法 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1996013331A1 true WO1996013331A1 (fr) | 1996-05-09 |
Family
ID=17411125
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP1995/002040 WO1996013331A1 (fr) | 1994-10-28 | 1995-10-05 | Catalyseur de conversion d'hydrocarbure et procede de conversion catalytique avec ce catalyseur |
Country Status (10)
Country | Link |
---|---|
US (1) | US5968342A (ja) |
EP (2) | EP0788838B1 (ja) |
JP (1) | JP3664502B2 (ja) |
KR (1) | KR100233194B1 (ja) |
CN (1) | CN1070733C (ja) |
DE (2) | DE69535660T2 (ja) |
MY (1) | MY121186A (ja) |
RU (1) | RU2133639C1 (ja) |
WO (1) | WO1996013331A1 (ja) |
ZA (1) | ZA958907B (ja) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2007032448A1 (ja) | 2005-09-16 | 2007-03-22 | Asahi Kasei Chemicals Corporation | エチレン及びプロピレンの製造方法 |
WO2007032447A1 (ja) * | 2005-09-16 | 2007-03-22 | Asahi Kasei Chemicals Corporation | エチレン及びプロピレンを製造する方法 |
JP2007106739A (ja) * | 2005-09-16 | 2007-04-26 | Asahi Kasei Chemicals Corp | エチレン及びプロピレンを製造する方法 |
WO2007080957A1 (ja) | 2006-01-16 | 2007-07-19 | Asahi Kasei Chemicals Corporation | プロピレン及び芳香族炭化水素の製造方法並びにその製造装置 |
WO2007088745A1 (ja) * | 2006-01-31 | 2007-08-09 | Asahi Kasei Chemicals Corporation | 芳香族炭化水素化合物製造用触媒 |
US9079168B2 (en) | 2007-09-06 | 2015-07-14 | Asahi Kasei Chemicals Corporation | Process for producing propylene |
US9192922B2 (en) | 2007-09-18 | 2015-11-24 | Asahi Kasei Chemicals Corporation | Propylene production process |
Families Citing this family (38)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE19981583B3 (de) * | 1998-08-25 | 2014-06-05 | Asahi Kasei Kabushiki Kaisha | Verfahren zur Herstellung von Ethylen und Propylen |
DE60109704D1 (de) * | 2000-10-25 | 2005-05-04 | Mitsubishi Chem Corp | Verfahren zur Oxidation von Olefinen unter Verwendung eines Silber und Alkalimetall(e) enthaltenden Katalysator |
RU2203735C1 (ru) * | 2001-11-20 | 2003-05-10 | Общество с ограниченной ответственностью "Руно золотое" | Способ получения цеолитсодержащего катализатора |
US7347930B2 (en) * | 2003-10-16 | 2008-03-25 | China Petroleum & Chemical Corporation | Process for cracking hydrocarbon oils |
CZ298836B6 (cs) * | 2004-04-15 | 2008-02-20 | Výzkumný ústav anorganické chemie, a. s. | Zeolitový katalyzátor struktury ZSM-5 pro selektivní krakování alkenu a zpusob jeho výroby |
KR20050102766A (ko) * | 2004-04-22 | 2005-10-27 | 주식회사 엘지화학 | 탄화수소 분해촉매 및 그 제조방법 |
GB0414442D0 (en) * | 2004-06-28 | 2004-07-28 | Borealis As | Zeolite catalysts |
CN101006035B (zh) * | 2004-07-16 | 2012-08-08 | 旭化成化学株式会社 | 制造乙烯和丙烯的方法 |
US7615143B2 (en) * | 2004-07-30 | 2009-11-10 | Exxonmobil Chemical Patents Inc. | Hydrothermally stable catalyst and its use in catalytic cracking |
KR100638444B1 (ko) * | 2004-10-18 | 2006-10-24 | 주식회사 엘지화학 | 화학액상 증착법을 이용한 탄화수소 분해촉매 및 그제조방법 |
CA2633900A1 (en) * | 2005-12-01 | 2007-06-07 | Basf Catalysts Llc | Hydrothermally stable ag-zeolite traps for for small olefin hydrocarbon molecules |
EP2024308A1 (en) * | 2006-05-19 | 2009-02-18 | Shell Internationale Research Maatschappij B.V. | Process for the preparation of propylene from a hydrocarbon feed |
US8049054B2 (en) | 2006-05-19 | 2011-11-01 | Shell Oil Company | Process for the preparation of C5 and/or C6 olefin |
EP2024303B1 (en) | 2006-05-19 | 2012-01-18 | Shell Internationale Research Maatschappij B.V. | Process for the preparation of an olefin |
CN101448765A (zh) | 2006-05-19 | 2009-06-03 | 国际壳牌研究有限公司 | 环烯烃的烷基化方法 |
CN101448768B (zh) | 2006-05-19 | 2013-05-22 | 国际壳牌研究有限公司 | 丙烯的制备方法 |
BRPI0819631A2 (pt) | 2007-11-19 | 2015-05-05 | Shell Int Research | Processo para a preparação de um produto olefínico |
US20100331590A1 (en) * | 2009-06-25 | 2010-12-30 | Debarshi Majumder | Production of light olefins and aromatics |
CN102050462B (zh) * | 2009-10-30 | 2012-10-17 | 中国石油天然气股份有限公司 | 一种提高水热稳定性的双组元改性分子筛及制备方法 |
US20110230333A1 (en) * | 2010-03-16 | 2011-09-22 | Uop Llc | Olefin Cracking Catalyst and Manufacturing Process |
RU2449978C1 (ru) * | 2010-12-17 | 2012-05-10 | Ирина Игоревна Иванова | Способ ароматизации неароматических углеводородов |
KR101298871B1 (ko) * | 2011-02-24 | 2013-08-21 | 롯데케미칼 주식회사 | 에틸렌 및 프로필렌 제조방법 |
CN103813856B (zh) * | 2011-07-21 | 2016-08-10 | 瑞来斯实业有限公司 | 流化床催化裂化(fcc)催化剂添加剂及其制备方法 |
US9745519B2 (en) | 2012-08-22 | 2017-08-29 | Kellogg Brown & Root Llc | FCC process using a modified catalyst |
RU2508164C1 (ru) * | 2012-12-25 | 2014-02-27 | ФЕДЕРАЛЬНОЕ ГОСУДАРСТВЕННОЕ БЮДЖЕТНОЕ УЧРЕЖДЕНИЕ НАУКИ ИНСТИТУТ ОРГАНИЧЕСКОЙ ХИМИИ им. Н.Д. ЗЕЛИНСКОГО РОССИЙСКОЙ АКАДЕМИИ НАУК (ИОХ РАН) | Способ приготовления катализатора для получения бензола из метана, катализатор, приготовленный по этому способу, и способ получения бензола из метана с использованием полученного катализатора |
EP2991762B1 (en) | 2013-04-29 | 2022-11-16 | Saudi Basic Industries Corporation | Catalytic methods for converting naphtha into olefins |
EP3337776B1 (en) * | 2015-08-21 | 2019-06-05 | SABIC Global Technologies B.V. | Process for producing btx from a c5-c12 hydrocarbon mixture |
CZ306416B6 (cs) * | 2015-09-03 | 2017-01-11 | Unipetrol Výzkumně Vzdělávací Centrum, A. S. | Způsob výroby dutých kulových částic zeolitu ZSM-5 |
CN109071378B (zh) * | 2016-04-11 | 2022-08-05 | 旭化成株式会社 | 低级烯烃的制造方法 |
WO2018173269A1 (ja) * | 2017-03-24 | 2018-09-27 | 日揮株式会社 | ゼオライト含有触媒および低級オレフィンの製造方法 |
JP7348716B2 (ja) * | 2017-05-31 | 2023-09-21 | 古河電気工業株式会社 | ナフサから生成されるオレフィン製造用触媒構造体、該触媒構造体を備えるオレフィン製造装置及びオレフィン製造用触媒構造体の製造方法 |
JP7348717B2 (ja) * | 2017-05-31 | 2023-09-21 | 古河電気工業株式会社 | ブテンから生成されるオレフィン製造用触媒構造体、該触媒構造体を有するオレフィン製造装置及びオレフィン製造用触媒構造体の製造方法 |
KR102079063B1 (ko) * | 2018-06-20 | 2020-04-13 | 한국화학연구원 | 경질올레핀 제조용 촉매, 이의 제조방법, 및 이를 이용하여 경질올레핀을 제조하는 방법 |
JP7110792B2 (ja) * | 2018-07-26 | 2022-08-02 | 東ソー株式会社 | 銀イオン交換ゼオライトの製造方法 |
JP7443684B2 (ja) | 2019-07-10 | 2024-03-06 | 東ソー株式会社 | 新規ゼオライト及びそれを含む芳香族炭化水素製造用触媒 |
US11648540B2 (en) * | 2021-01-25 | 2023-05-16 | China Energy Investment Corporation Limited | Modified catalyst, method for preparing the same, and method for producing aromatic hydrocarbons by aromatization of olefins |
CN113333014A (zh) * | 2021-06-02 | 2021-09-03 | 辽宁师范大学 | 用于乙苯乙醇/乙烯烷基化制二乙苯的固体催化剂及制备方法 |
CN114988978B (zh) * | 2022-06-20 | 2024-04-30 | 常州大学 | 一种利用非均相催化剂催化3-芳基丙醇一步合成1-丙烯基芳烃的新方法 |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61157353A (ja) * | 1984-12-28 | 1986-07-17 | モービル オイル コーポレーシヨン | 水熱的に安定なゼオライト触媒の製造方法 |
JPH0417165B2 (ja) * | 1984-06-22 | 1992-03-25 | Keishitsu Ryubun Shinyoto Kaihatsu Gijutsu Kenkyu Kumiai | |
JPH05139724A (ja) * | 1991-11-21 | 1993-06-08 | Idemitsu Kosan Co Ltd | 金属含有結晶質アルミノシリケートの製造方法 |
Family Cites Families (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3702886A (en) * | 1969-10-10 | 1972-11-14 | Mobil Oil Corp | Crystalline zeolite zsm-5 and method of preparing the same |
US3775501A (en) * | 1972-06-05 | 1973-11-27 | Mobil Oil Corp | Preparation of aromatics over zeolite catalysts |
US3890218A (en) * | 1974-03-29 | 1975-06-17 | Mobil Oil Corp | Upgrading aliphatic naphthas to higher octane gasoline |
GB1522793A (en) * | 1974-07-31 | 1978-08-31 | Black D S C | Metal complex dyestuffs and pigments |
US4276438A (en) * | 1980-05-27 | 1981-06-30 | Mobil Oil Corporation | Shape selective reactions with group IB modified zeolite catalysts |
US4347394A (en) * | 1980-12-10 | 1982-08-31 | Chevron Research Company | Benzene synthesis |
US4458097A (en) * | 1982-04-30 | 1984-07-03 | Union Carbide Corporation | Conversion of certain hydrocarbons using divalent-copper-containing ZSM-5 type catalyst |
NZ205859A (en) * | 1982-10-15 | 1986-04-11 | Mobil Oil Corp | Organic conversion using zeolite catalyst |
US4608355A (en) * | 1983-08-10 | 1986-08-26 | Mobil Oil Corporation | Hydrocarbon conversion catalyst |
CN1012880B (zh) * | 1984-11-05 | 1991-06-19 | 环球油品公司 | 用于烃转化的催化复合物 |
JP2801686B2 (ja) * | 1989-10-16 | 1998-09-21 | 旭化成工業株式会社 | 炭化水素の接触転化法 |
AU649586B2 (en) * | 1990-03-09 | 1994-05-26 | Tosoh Corporation | Catalyst and method for catalytically decomposing nitrogen oxides |
US5103066A (en) * | 1990-12-10 | 1992-04-07 | Mobil Oil Corp. | Dehydrogenation of alcohols over non-acidic metal-zeolite catalysts |
JP2973524B2 (ja) * | 1990-12-18 | 1999-11-08 | 東ソー株式会社 | 排ガス浄化触媒 |
US5316661A (en) * | 1992-07-08 | 1994-05-31 | Mobil Oil Corporation | Processes for converting feedstock organic compounds |
US5312995A (en) * | 1993-04-23 | 1994-05-17 | Arco Chemical Technology, L.P. | Process for isomerizing epoxides to aldehydes |
US5292976A (en) * | 1993-04-27 | 1994-03-08 | Mobil Oil Corporation | Process for the selective conversion of naphtha to aromatics and olefins |
US5592085A (en) * | 1994-10-19 | 1997-01-07 | Mayo Foundation For Medical Education And Research | MR imaging of synchronous spin motion and strain waves |
-
1994
- 1994-10-28 JP JP26499694A patent/JP3664502B2/ja not_active Expired - Lifetime
-
1995
- 1995-10-05 RU RU97108555A patent/RU2133639C1/ru active
- 1995-10-05 CN CN95195893A patent/CN1070733C/zh not_active Expired - Lifetime
- 1995-10-05 KR KR1019970702809A patent/KR100233194B1/ko not_active IP Right Cessation
- 1995-10-05 WO PCT/JP1995/002040 patent/WO1996013331A1/ja active IP Right Grant
- 1995-10-05 EP EP95933621A patent/EP0788838B1/en not_active Expired - Lifetime
- 1995-10-05 DE DE69535660T patent/DE69535660T2/de not_active Expired - Lifetime
- 1995-10-05 EP EP05021950A patent/EP1642641B1/en not_active Expired - Lifetime
- 1995-10-05 US US08/809,830 patent/US5968342A/en not_active Expired - Lifetime
- 1995-10-05 DE DE69534721T patent/DE69534721T2/de not_active Expired - Lifetime
- 1995-10-18 MY MYPI95003124A patent/MY121186A/en unknown
- 1995-10-20 ZA ZA958907A patent/ZA958907B/xx unknown
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0417165B2 (ja) * | 1984-06-22 | 1992-03-25 | Keishitsu Ryubun Shinyoto Kaihatsu Gijutsu Kenkyu Kumiai | |
JPS61157353A (ja) * | 1984-12-28 | 1986-07-17 | モービル オイル コーポレーシヨン | 水熱的に安定なゼオライト触媒の製造方法 |
JPH05139724A (ja) * | 1991-11-21 | 1993-06-08 | Idemitsu Kosan Co Ltd | 金属含有結晶質アルミノシリケートの製造方法 |
Non-Patent Citations (1)
Title |
---|
See also references of EP0788838A4 * |
Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5014138B2 (ja) * | 2005-09-16 | 2012-08-29 | 旭化成ケミカルズ株式会社 | エチレン及びプロピレンを製造する方法 |
WO2007032447A1 (ja) * | 2005-09-16 | 2007-03-22 | Asahi Kasei Chemicals Corporation | エチレン及びプロピレンを製造する方法 |
JP2007106739A (ja) * | 2005-09-16 | 2007-04-26 | Asahi Kasei Chemicals Corp | エチレン及びプロピレンを製造する方法 |
US7884257B2 (en) | 2005-09-16 | 2011-02-08 | Asahi Kasei Chemicals Corporation | Method for producing ethylene and propylene |
US7893311B2 (en) | 2005-09-16 | 2011-02-22 | Asahi Kasei Chemicals Corporation | Method for producing ethylene and propylene |
WO2007032448A1 (ja) | 2005-09-16 | 2007-03-22 | Asahi Kasei Chemicals Corporation | エチレン及びプロピレンの製造方法 |
WO2007080957A1 (ja) | 2006-01-16 | 2007-07-19 | Asahi Kasei Chemicals Corporation | プロピレン及び芳香族炭化水素の製造方法並びにその製造装置 |
US8034987B2 (en) | 2006-01-16 | 2011-10-11 | Asahi Kasei Chemicals Corporation | Process for producing propylene and aromatic hydrocarbons, and producing apparatus therefor |
WO2007088745A1 (ja) * | 2006-01-31 | 2007-08-09 | Asahi Kasei Chemicals Corporation | 芳香族炭化水素化合物製造用触媒 |
KR100969263B1 (ko) * | 2006-01-31 | 2010-07-09 | 아사히 가세이 케미칼즈 가부시키가이샤 | 방향족 탄화수소 화합물 제조용 촉매 |
JP5179882B2 (ja) * | 2006-01-31 | 2013-04-10 | 旭化成ケミカルズ株式会社 | 芳香族炭化水素化合物製造用触媒 |
US9079168B2 (en) | 2007-09-06 | 2015-07-14 | Asahi Kasei Chemicals Corporation | Process for producing propylene |
US9192922B2 (en) | 2007-09-18 | 2015-11-24 | Asahi Kasei Chemicals Corporation | Propylene production process |
Also Published As
Publication number | Publication date |
---|---|
DE69534721D1 (de) | 2006-02-02 |
CN1070733C (zh) | 2001-09-12 |
MY121186A (en) | 2006-01-28 |
KR970706898A (ko) | 1997-12-01 |
EP0788838B1 (en) | 2005-12-28 |
ZA958907B (en) | 1996-05-14 |
EP1642641B1 (en) | 2007-12-05 |
EP0788838A1 (en) | 1997-08-13 |
CN1162274A (zh) | 1997-10-15 |
DE69535660D1 (de) | 2008-01-17 |
DE69535660T2 (de) | 2008-11-13 |
JPH08127546A (ja) | 1996-05-21 |
EP1642641A1 (en) | 2006-04-05 |
EP0788838A4 (en) | 1999-08-11 |
KR100233194B1 (ko) | 1999-12-01 |
DE69534721T2 (de) | 2006-09-07 |
JP3664502B2 (ja) | 2005-06-29 |
RU2133639C1 (ru) | 1999-07-27 |
US5968342A (en) | 1999-10-19 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
WO1996013331A1 (fr) | Catalyseur de conversion d'hydrocarbure et procede de conversion catalytique avec ce catalyseur | |
EP0772492B1 (en) | Para-xylene selective reforming/aromatization | |
EP0027157B1 (en) | Process for selective dealkylation of alkyl-substituted aromatic hydrocarbons | |
US5866741A (en) | Transalkylation/hydrodealkylation of a C9 + aromatic compounds with a zeolite | |
US7026263B2 (en) | Hybrid catalysts for the deep catalytic cracking of petroleum naphthas and other hydrocarbon feedstocks | |
JPH0816074B2 (ja) | キシレン異性化法 | |
US5804059A (en) | Process of preparing a C6 to C8 hydrocarbon with a steamed, acid-leached, molybdenum containing mordenite catalyst | |
US5013423A (en) | Reforming and dehydrocyclization | |
US7510644B2 (en) | Zeolites and molecular sieves and the use thereof | |
CA2285410C (en) | Process for the conversion of hydrocarbons to olefins and aromatics | |
US5883033A (en) | Hydrocarbon conversion catalyst composition and processes therefor and therewith | |
US5929295A (en) | Hydrodealkylation and transalkylation of C9 + aromatic compounds | |
JP3741455B2 (ja) | 炭化水素転化触媒並びにこれを用いる低級オレフィン及び単環芳香族炭化水素の製造方法 | |
CA2021487C (en) | Process for the obtainment of a light paraffin isomerization catalyst | |
JP3966429B2 (ja) | 芳香族炭化水素製造用触媒 | |
JP3068347B2 (ja) | 高オクタン価ガソリン基材の製造方法 | |
US6013849A (en) | Toluene disproportionation process using a zeolite/tungsten carbide catalyst | |
US5264648A (en) | Process for the obtainment of a light paraffin isomerization catalyst | |
JPH0417165B2 (ja) | ||
JPH0729948B2 (ja) | 芳香族炭化水素の製造法 | |
JP3472184B2 (ja) | ベンゼンの他の芳香族炭化水素への変換方法 | |
CA2473751C (en) | Hybrid catalysts for the deep catalytic cracking of petroleum naphthas and other hydrocarbon feedstocks | |
JPH0541611B2 (ja) | ||
MXPA99009962A (en) | Process for the conversion of hydrocarbons to olefins and aromatics |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
WWE | Wipo information: entry into national phase |
Ref document number: 95195893.3 Country of ref document: CN |
|
AK | Designated states |
Kind code of ref document: A1 Designated state(s): CN KR RU SG US |
|
AL | Designated countries for regional patents |
Kind code of ref document: A1 Designated state(s): AT BE CH DE DK ES FR GB GR IE IT LU MC NL PT SE |
|
DFPE | Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101) | ||
121 | Ep: the epo has been informed by wipo that ep was designated in this application | ||
WWE | Wipo information: entry into national phase |
Ref document number: 08809830 Country of ref document: US |
|
WWE | Wipo information: entry into national phase |
Ref document number: 1995933621 Country of ref document: EP |
|
WWE | Wipo information: entry into national phase |
Ref document number: 1019970702809 Country of ref document: KR |
|
WWP | Wipo information: published in national office |
Ref document number: 1995933621 Country of ref document: EP |
|
WWP | Wipo information: published in national office |
Ref document number: 1019970702809 Country of ref document: KR |
|
WWG | Wipo information: grant in national office |
Ref document number: 1019970702809 Country of ref document: KR |
|
WWG | Wipo information: grant in national office |
Ref document number: 1995933621 Country of ref document: EP |