WO2000018853A1 - Process for manufacturing olefins using a pentasil zeolite based catalyst - Google Patents
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- WO2000018853A1 WO2000018853A1 PCT/US1999/022460 US9922460W WO0018853A1 WO 2000018853 A1 WO2000018853 A1 WO 2000018853A1 US 9922460 W US9922460 W US 9922460W WO 0018853 A1 WO0018853 A1 WO 0018853A1
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- 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
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- 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
- B01J29/061—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof containing metallic elements added to the zeolite
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- 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
- B01J29/405—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 rare earth elements, titanium, zirconium, hafnium, zinc, cadmium, mercury, gallium, indium, thallium, tin or lead
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- 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
- B01J29/82—Phosphates
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- 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
- B01J2229/00—Aspects of molecular sieve catalysts not covered by B01J29/00
- B01J2229/10—After treatment, characterised by the effect to be obtained
- B01J2229/26—After treatment, characterised by the effect to be obtained to stabilize the total catalyst structure
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- 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
- B01J2229/00—Aspects of molecular sieve catalysts not covered by B01J29/00
- B01J2229/30—After treatment, characterised by the means used
- B01J2229/42—Addition of matrix or binder particles
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- 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
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- 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
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P30/00—Technologies relating to oil refining and petrochemical industry
- Y02P30/40—Ethylene production
Definitions
- the invention is a naphtha cracking catalyst and an improved catalytic naphtha cracking process for producing olefins from paraffins, particularly paraffins which are present in a hydrocarbon mixture commonly known as naphtha.
- the process provides relatively higher propylene yields and significantly lower methane yields over the commercially important range of about 60 to about 90 percent naphtha conversion, while providing about the same or lower yields of aromatics and light paraffins over the range, as compared to well known prior art catalytic and thermal processes. Additionally, the process resists deactivation of the catalyst by coking.
- the invention is a process for producing a relatively light olefin.
- Naphtha is the preferred feedstock for this process.
- a hydrocarbon feedstock which includes hydrocarbons having about three to about twenty carbon atoms, preferably paraffinic and isoparaffinic hydrocarbons having about four to about eleven carbon atoms per molecule, is passed into a reactor containing a pentasil zeolite catalyst.
- the zeolite-containing catalyst typically includes about 0.1 to about 10 weight percent phosphorus and about 0.1 to about 10 weight percent of a promoter metal selected from the group consisting of gallium, germanium, tin and mixtures thereof.
- At least a portion of the hydrocarbon is converted to produce an olefin having about two to about three carbon atoms per molecule.
- the hydrocarbon may be passed into the reactor together with a heat-conducting diluent such as steam, nitrogen, alkanes such as methane and ethane, and mixtures thereof which are substantially inert under the process conditions used.
- the invention is a process for producing an olefin, which process comprises contacting a naphtha which includes a paraffin having about four to about eleven carbon atoms per molecule with a catalyst in a reactor at a temperature of about 400 to about 650 degrees C. and a pressure of about one to about three atmospheres.
- the catalyst is a pentasil zeolite catalyst having a silicon to aluminum atomic ratio of about 10 to about 400 and on which is typically placed about 0.1 to about 10 weight percent phosphorus and about 0.1 to about 10 weight percent of a promoting metal selected from the group consisting of germanium, gallium, tin, and mixtures thereof.
- At least a portion of the naphtha is cracked in the reactor to produce olefins having about two to about three carbon atoms per molecule.
- the naphtha may be passed into the reactor together with a diluent in the molar ratio in the range of about 9 to about 0.1.
- the naphtha may be passed into the reactor together with additional propane in a molar ratio in the range of about 6 to about 1.
- a portion of the reactor product may be recycled to the reactor.
- the invention is a catalyst useful for producing light olefins from a hydrocarbon mixture, such as a naphtha, which includes one or more paraffins.
- the catalyst comprises a pentasil zeolite comprising silicon and aluminum in a silicon to aluminum atomic ratio of about 10 to about 400, about 0.1 to about 10 weight percent phosphorus, and about 0.1 to about 10 weight percent of a promoter metal selected from the group consisting of germanium, gallium, tin, and mixtures thereof.
- the pentasil zeolite is ZSM-5.
- Fig. 1 is a graph showing ethylene yield as a function of naphtha conversion catalyzed by phosphorus on HZSM-5 zeolite of silicon to aluminum atomic ratio equal to 30, and by phosphorus on HZSM-5 zeolite of silicon to aluminum atomic ratio equal to 30 with gallium, respectively;
- Fig. 2 is a graph showing propylene yield as a function of naphtha conversion catalyzed by phosphorus on HZSM-5 zeolite of silicon to aluminum atomic ratio equal to 30, and by phosphorus on HZSM-5 zeolite of silicon to aluminum atomic ratio equal to 30 with gallium, respectively;
- Fig. 3 is a graph showing aromatics yield as a function of naphtha conversion catalyzed by phosphorus on HZSM-5 zeolite of silicon to aluminum atomic ratio equal to 30, and by phosphorus on HZSM-5 zeolite of silicon to aluminum atomic ratio equal to 30 with gallium, respectively;
- Fig. 4 is a graph showing the weight ratio of C, through C 3 paraffins produced to C 2 through C 3 olefins produced as a function of naphtha conversion catalyzed by phosphorus on HZSM-5 zeolite of silicon to aluminum atomic ratio equal to 30, and by phosphorus on HZSM-5 zeolite of silicon to aluminum atomic ratio equal to 30 with gallium, respectively;
- Fig. 5 is a graph showing ethylene yield as a function of naphtha conversion catalyzed by phosphorus on HZSM-5 zeolite of silicon to aluminum atomic ratio equal to 60, and by phosphorus on HZSM-5 zeolite of silicon to aluminum atomic ratio equal to 60 with gallium, germanium or tin, respectively;
- Fig. 6 is a graph showing propylene yield as a function of naphtha conversion catalyzed by phosphorus on HZSM-5 zeolite of silicon to aluminum atomic ratio equal to 60, and by phosphorus on HZSM-5 zeolite of silicon to aluminum atomic ratio equal to 60 with gallium, germanium or tin, respectively;
- Fig. 7 is a graph showing aromatics yield as a function of naphtha conversion catalyzed by phosphorus on HZSM-5 zeolite of silicon to aluminum atomic ratio equal to 60, and by phosphorus on HZSM-5 zeolite of silicon to aluminum atomic ratio equal to 60 with gallium, germanium or tin, respectively; and Fig.
- FIG. 8 is a graph showing the weight ratio of C, through C 3 paraffins produced to C 2 through C 3 olefins produced as a function of naphtha conversion catalyzed by phosphorus on HZSM-5 zeolite of silicon to aluminum atomic ratio equal to 60, and by phosphorus on HZSM-5 zeolite of silicon to aluminum atomic ratio equal to 60 with gallium, germanium or tin, respectively.
- the present invention is a process in which a hydrocarbon feedstock comprising paraffins, aromatics, naphthenes, or mixtures thereof, is at least partially catalytically cracked to produce valuable lower olefins such as, for example, ethylene, propylene and butylene.
- the process includes contacting the hydrocarbon feedstock at effective reaction conditions with a pentasil zeolite catalyst which includes phosphorus and a promoter metal selected from the group consisting of gallium, germanium, tin and mixtures thereof.
- naphthas comprise the most suitable feedstock materials.
- Naphtha means a volatile hydrocarbon mixture which is liquid at room temperature and pressure.
- Preferred naphthas comprise one or more paraffins, each of the paraffins having about three to about twenty carbon atoms per molecule, more preferably about four to about eleven carbon atoms per molecule, and exhibit an atmospheric volumetric average boiling point in the range of about negative 22 to about 466 degrees C , more preferably about negative 1 to about 204 degrees C.
- paraffin means a saturated hydrocarbon of the empirical chemical formula C n H 2n+2 wherein n is an integer greater than zero.
- Paraffins include normal paraffins, which are unbranched, and isoparaffins, which contain at least one branched carbon chain per molecule.
- Especially preferred naphthas comprise proportions of various hydrocarbons present in the following ranges, expressed in weight percent of the total naphtha weight: Normal Paraffins Isoparaffins Naphthenes Olefins Aromatics
- contacting of the hydrocarbon feedstock and the pentasil zeolite catalyst is carried out at conditions which favor the formation of lower olefins.
- the hydrocarbon feedstock and the pentasil zeolite catalyst which is described in more detail below, are contacted in a reactor.
- reactor means an apparatus such as, for example, a vessel, a tube, a riser or a coil, which encloses a volume which is maintained at reaction conditions effective to promote a desired chemical reaction.
- the invention may be practiced utilizing any of various types of reactors, some of which are known in the art as, for example, a fixed bed down flow reactor with feed preheating, a radial flow reactor, a fluidized bed reactor, or a transport riser reactor.
- the process of the instant invention is highly endothermic.
- fluidized bed solid catalyst conversion procedures are used in which the feed hydrocarbon material is contacted in vapor form with fluidized catalyst particles comprising pentasil zeolite catalyst.
- this aspect of the invention can be successfully practiced using fixed bed procedures.
- a fixed bed of catalyst is employed, the use of reactors in series with interstage heating is advantageous.
- Moving catalyst bed technology such the catalyst regenerating technology employed commercially for the reforming of naphtha fractions, may be advantageously employed with the instant invention.
- a preferred reactor system is a moving bed radial flow multi-stage reactor with interstage heating, as described in U.S. Patent No.s 3,652,231; 4,094,814; 4,110,081 ; and 4,403,909, which are hereby incorporated by reference in their entirety, and specifically for their teachings regarding moving catalyst bed technology and regeneration systems.
- This reactor system normally employs a spherical catalyst having a diameter of about 0.03 to about 0.13 of an inch (about 0.76 to about 3.3 millimeter).
- effective reaction conditions means conditions which favor the formation of lower olefins.
- Conditions which favor the formation of lower olefins and, therefore, should be maintained in the reactor include a temperature of about 400 to about 650 degrees C, preferably about 480 to about 635 degrees C, more preferably about 540 to about 620 degrees C , and most preferably about 540 to about 600 degrees C.
- the total pressure in the reactor of this preferred aspect of the invention typically about 1 to about 2 atmospheres absolute, more preferably about 1 to about 1.5 atmospheres absolute, most preferably about 1 to about 1.15 atmospheres absolute.
- the partial pressure attributable to all hydrocarbons present in the reactor at effective reaction conditions is about 0.1 to about 0.9 atmospheres absolute.
- the hydrocarbon feedstock may be admixed with a diluent useful for heat transfer composed of nitrogen, steam or a relatively refractory hydrocarbon such as, for example, methane or ethane.
- the partial pressure of the diluent at effective reaction conditions may be from about 0.9 to about 0.1 atmospheres absolute.
- the hydrocarbon feedstock may be admixed with a co-feed composed substantially of propane.
- the hydrocarbon feedstock and the co-feed are passed into the reactor together, and the molar ratio of propane passed into the reactor to the hydrocarbon passed into the reactor is preferably about 6 to about 1. Some portion of reactor products may be recycled back to the reactor.
- space time in the reactor is about 1 to about 180 grams of catalyst per mole of hydrocarbon feedstock per hour, more preferably about 50 to about 100 grams of catalyst per mole of hydrocarbon feedstock per hour.
- space time means the mass of catalyst in grams present in the reactor for each mole per hour of hydrocarbon feedstock which enters the reactor.
- the invention is a catalyst.
- the active catalyst component is a phosphorus-containing pentasil zeolite such as, for example, ZSM-5 zeolite or ZSM-11 zeolite.
- zeolite means a crystalline molecular sieve, which has an open porous structure and an ion exchange capacity.
- a zeolite may contain elements in addition to silicon and aluminum in their framework structures.
- a zeolite may be a silicate having a framework structure into which a relatively small quantity of another element has been substituted, such as aluminum in ZSM-5 aluminosilicalite or boron in HAMS-l-B borosilicate.
- Silicalite is described in U.S Patent No. 4,061,724, which is hereby incorporated by reference in its entirety, and especially for its teachings regarding silicalite.
- HAMS-l-B is described in U.S Patent No. 4,269,813, which is hereby incorporated by reference in its entirety, and especially for its teachings regarding HAMS-IB.
- Pentasil means a family of zeolites having similar framework structures with ZSM-5 and ZSM-11 as its two end members.
- the framework structures are formed by linking chains of 5-membered ring secondary building units. Further information regarding pentasil zeolites may be found at pages 12-14 of Shape Selective Catalysis in Industrial Applications by N.Y. Chen et al., copyright 1989, published by Marcel Dekker, Inc. of New York.
- the pentasil zeolite useful in this invention also includes a promoter metal selected from the group consisting of gallium, germanium, tin, and mixtures thereof.
- the zeolite is a phosphorus-containing ZSM-5 having a surface silicon to aluminum atomic ratio in the range of about 10 to about 400, preferably about 30 to about 180, and more preferably about 30 to about 60.
- the silicon to aluminum atomic ratio of the zeolite is conveniently controlled by regulating the amounts of components which are used to formulate the zeolite in accordance with known procedures.
- phosphorus may be added to the formed pentasil zeolite by impregnating the zeolite with a phosphorus compound in accordance with the procedures described, for example, in U.S. Patent No. 3,972,832 and U.S. Patent No. 5,171,921 (which patents are incorporated herein by reference in their entirety, and especially for their teachings regarding pentasil zeolite).
- the phosphorus compound can be added to a multicomponent mixture from which the pentasil catalyst is formed.
- the phosphorus compound is added in an amount sufficient to provide a final pentasil zeolite composition having preferably about 0.1 to about 10 weight percent phosphorus, more preferably about 0.5 to about 2 weight percent phosphorus, most preferably about 0.75 to about 1.5 weight percent phosphorus, and usually about 1 weight percent phosphorus, based on the total weight of the pentasil zeolite.
- the promoter metal may be incorporated into the phosphorus-containing pentasil zeolite (hereinafter referred to as "P-pentasil zeolite") by any suitable manner known in the art which results in a relatively uniform dispersion of the second metal such as, for example, by ion exchange, cogelation, or impregnation.
- the promoter is added in an amount sufficient to provide a final P-pentasil zeolite having preferably about 0.1 to about 10 weight percent of the promoter metal, more preferably about 0.5 to about 5 weight percent of the promoter metal, most preferably about 0.75 to about 2 weight percent of the promoter metal, and ideally about 1 weight percent of the promoter metal based on the total weight of the pentasil zeolite.
- the phosphorus-containing pentasil zeolite described in this invention is preferably combined with or incorporated into known inert binders or matrices such as alumina, silica and silica alumina and may be formed into pellets, spheres or other discrete forms suitable for use in a hydrocarbon conversion reactor.
- a pentasil zeolite product may be formed into discrete forms by extruding from a die and chopping. Typical extrudates may be about 1 to about 10 millimeters in diameter, often about 2 to about 6 millimeters in diameter, and about 4 to about 20 millimeters in length as suitable for the reactor system utilized.
- a zeolite binder product may be formed into a sphere by rolling or by dropping in a liquid filled tower. Typical spheres are about 0.03 to about 0.5 inches (about 0.75 to about 12 millimeters) in diameter.
- a pentasil zeolite is modified by incorporation of phosphorus and a promoter metal species.
- phosphorus is incorporated by adding a suitable phosphorus containing compound to the zeolite-containing material in a liquid medium, followed by drying and calcining.
- the promoter metal may be incorporated by methods including impregnation and ion exchange, either to the zeolite alone or to the zeolite incorporated into the binder.
- one or more of the promoter metals may be added to the binder or to the zeolite- binder product.
- the binder or matrix generally comprises about 5 to about 90 weight percent of the catalyst composition, preferably about 20 to about weight percent, and more preferably about 30 to about 50 weight percent.
- the phosphorus- containing pentasil zeolite need not be treated with steam after incorporation of phosphorus.
- naphtha conversion means a mole- weighted average of the individual conversions of fifteen non-aromatic key components which are present in the naphtha but are not created under reaction conditions.
- the use of the key components in calculating naphtha conversion tends to minimise ambiguities which might otherwise arise when individual components are simultaneously created and destroyed in the same reactor. More information regarding the determination of naphtha conversion may be found in a technical paper entitled “Scaling Up of Naphtha Cracking Coils" by P.S. Van Damme, G.F. Froment, and W.S. Balthasar which appears in Industrial Engineering Chemistry Process Design and Development, 1981, vol. 20, at page 366, which is incorporated by reference herein.
- Example 1 Conversion of Naphtha over 1 weight percent P on HZSM-5 zeolite of Silicon to Aluminum Atomic Ratio 30
- Naphtha Feed Composition (weight percent) hydrogen 0.00 2, 2-dimethylbutane 2.83 methane 0.00 2, 3-dimethylbutane 3.50 ethylene (C2H4) 0.00 cyclohexane 0.52 ethane 0.00 2, 2-dimethylpentane 1.38 propylene (C3H6) 0.00 2, 4-dimethylpentane 1.65 propane 0.00 3, 3-dimethylpentane 1.53 butylene (C4H8) 0.05 2, 3-dimethylpentane 2.74 i-butane 0.08 2-methylhexane 11.87 n-butane 0.12 3-methylhexane 12.07 pentane 0.10 3-ethylpentane 1.74 cyclopentane 1.36 n-heptane 0.65 i-pentane 2.51 methylcyclohexane 0.46 n-pentane 1.28 benzene 0.96 hexene 0.70 toluene 0.19 n-hexane 4.
- the 1 weight percent P on HZSM-5 zeolite was obtained from NH 4 -ZSM- 5 zeolite by means of an incipient wetness impregnation technique with orthophosphoric acid. More specifically, NH 4 -ZSM-5 zeolite was intimately contacted with a solution including distilled water and orthophosphoric acid of chemical formula H 3 PO 4 , and then dried. The resulting 1 weight percent P on HZSM-5 zeolite had a surface silicon to aluminum atomic ratio of 30.
- the 1 weight percent P on HZSM-5 zeolite of silicon to aluminum atomic ratio equal to 30 so obtained was utilised as a catalyst in the conversion of naphtha in a reactor at 540 °C and 1.05 bar absolute.
- the partial pressure of the naphtha at the inlet of the reactor was set at 0.25 bar absolute by diluting the feed naphtha with nitrogen.
- the fraction of feed naphtha converted was controlled by varying space time in the reactor.
- Ethylene yields observed with 1 weight percent P on HZSM-5 zeolite of silicon to aluminum atomic ratio equal to 30, represented by dark-colored square- shaped symbols, are depicted as a function of naphtha conversion in Fig. 1.
- Propylene yields observed with 1 weight percent P on HZSM-5, represented by dark-colored square-shaped symbols, are depicted as a function of naphtha conversion in Fig. 2.
- Aromatic yields observed with 1 weight percent P on HZSM-5, represented by dark-colored square-shaped symbols, are depicted as a function of naphtha conversion in Fig. 3.
- Fig. 4 indicates that the above described advantages regarding ethylene, propylene and aromatics yields are accompanied by a relative decrease in the production of commercially less valuable light paraffins.
- Fig. 4 indicates that the weight ratio of C, through C 3 paraffins produced to C 2 through C 3 olefins produced was 72 percent for the catalyst containing gallium at 89.5 percent naphtha conversion, as compared to 92 percent at 91.8 percent conversion for the previously known catalyst without gallium.
- Ga-P on HZSM-5 zeolite catalysts were prepared from NH 4 -ZSM-5 zeolite with silicon to aluminum atomic ratios in the range of 30 to 180.
- the Ga-P on HZSM-5 zeolite catalysts so prepared included gallium in the range of 0.33 to 2 weight percent and phosphorus in the range of 0.33 to 2 weight percent, based on the total weight of the catalyst.
- the Ga-P on HZSM-5 zeolite catalysts were placed in a reactor at 540 degrees C. in which naphtha was converted to olefins, aromatics and paraffins.
- Feed rate through the reactor was varied. Operating periods of approximately equal feed conversion by weight at space times of 175.6, 87.9, 43.9, and 22.0 grams of catalyst per mol per hour of feed rate, respectively, are reported in descending order from top to bottom in Table 3, below. During such operating periods, naphtha conversion was in the range of 83.3 to 89.6 weight percent. Ethylene yield, propylene yield, butylene yield, aromatic yield and methane yield expressed in weight percent based on the total weight of the feed during such operating periods are reported below in Table 3.
- the data in Table 3 indicates that increasing the weight ratio of phosphorus to gallium increases yields of ethylene, propylene and butylenes. 5
- the data in Table 3 also indicates that increasing this weight ratio inhibits aromatic and methane production. Therefore, it is preferred that the weight ratio of phosphorus to gallium is in the range of about 1 : 1 to about 5:1 , more preferably about 2: 1 to about 3:1.
- Example 7 Conversion of Naphtha over 1 weight percent P on HZSM-5 l o zeolite of Silicon to Aluminum Atomic Ratio 60
- Example 20 and the naphtha conversion process utilised in this Example are substantially the same as described above in Example 1.
- Example 8 Conversion of naphtha over 1 weight percent Ga-1 weight percent P on HZSM-5 zeolite of Silicon to Aluminum Atomic Ratio 60
- a catalyst consisting of 1 weight percent Ga-1 weight percent P on HZSM-5 zeolite of silicon to aluminum atomic ratio equal to 60 was subsequently prepared by impregnating gallium onto a 1 weight percent P on HZSM-5 zeolite of silicon to aluminum atomic ratio equal to 60, which had been prepared by the method described above in Example 7.
- This catalyst was used to convert naphtha having the composition shown above in Table 2 at substantially the same conditions described above in Example 1. Again, naphtha conversion was controlled by varying space time in the reactor.
- Example 9 Conversion of naphtha over 1 weight percent Sn-1 weight percent P on HZSM-5 zeolite of Silicon to Aluminum Atomic Ratio 60
- the 1 weight percent Sn-1 weight percent P on HZSM-5 zeolite was utilised as a catalyst to promote the conversion of naphtha having the composition set forth above in Table 2, in a reactor maintained at substantially the conditions described above in Example 1.
- the weight ratio of C, through C 3 paraffins produced to C 2 through C 3 olefins produced over the catalyst represented by light-colored triangle-shaped symbols, is depicted as a function of naphtha conversion in Fig. 8.
- Example 4 An incipient wetness impregnation procedure, similar to the procedure described above in Example 4, was performed in which germanium was impregnated on 1 weight percent P on HZSM-5 having a silicon to aluminum atomic ratio of 60, calcined and reduced to produce 0.75 weight percent Ge-1 weight percent P on HZSM-5 zeolite of silicon to aluminum atomic ratio 60.
- the 0.75 weight percent Ge-1 weight percent P on HZSM-5 zeolite was utilised as a catalyst to promote the conversion of naphtha having the composition set forth above in Table 2, in a reactor maintained at substantially the conditions described above in Example 1.
- the Ga-P on HZSM-5 zeolite, the Sn-P on HZSM-5 zeolite and the 0.75 Ge-P on HZSM-5 zeolite are all effective catalysts for ethylene and propylene manufacturing by naphtha conversion. Moreover, the Sn-P on HZSM-5 zeolite is especially appropriate when low selectivities toward light paraffins are desired. When aromatics are not a primarily desired product, as in propylene manufacturing, the Ga-P on HZSM-5 zeolite is recommended because the zeolite suppresses aromatization while providing a relatively high yield of ethylene and propylene.
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Priority Applications (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AU62712/99A AU6271299A (en) | 1998-09-28 | 1999-09-28 | Process for manufacturing olefins using a pentasil zeolite based catalyst |
DE69918451T DE69918451T2 (en) | 1998-09-28 | 1999-09-28 | METHOD FOR THE PRODUCTION OF OLEFINES USING A PENTASIL ZEOLITE-CONTAINING CATALYST |
JP2000572303A JP2002525380A (en) | 1998-09-28 | 1999-09-28 | Olefin production using pentazyl zeolite based catalysts |
CA002345308A CA2345308A1 (en) | 1998-09-28 | 1999-09-28 | Process for manufacturing olefins using a pentasil zeolite based catalyst |
AT99949945T ATE270318T1 (en) | 1998-09-28 | 1999-09-28 | METHOD FOR PRODUCING OLEFINS USING A CATALYST CONTAINING PENTASIL ZEOLITE |
EP99949945A EP1117750B1 (en) | 1998-09-28 | 1999-09-28 | Process for manufacturing olefins using a pentasil zeolite based catalyst |
NO20011561A NO20011561D0 (en) | 1998-09-28 | 2001-03-27 | Process for the preparation of olefins using a pentasyl zeolite-based catalyst |
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US16184598A | 1998-09-28 | 1998-09-28 | |
US09/161,845 | 1998-09-28 | ||
US40558299A | 1999-09-27 | 1999-09-27 | |
US09/405,582 | 1999-09-27 |
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WO2000018853A1 true WO2000018853A1 (en) | 2000-04-06 |
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PCT/US1999/022460 WO2000018853A1 (en) | 1998-09-28 | 1999-09-28 | Process for manufacturing olefins using a pentasil zeolite based catalyst |
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US (1) | US6548725B2 (en) |
EP (1) | EP1117750B1 (en) |
JP (1) | JP2002525380A (en) |
CN (1) | CN1195714C (en) |
AT (1) | ATE270318T1 (en) |
AU (1) | AU6271299A (en) |
CA (1) | CA2345308A1 (en) |
DE (1) | DE69918451T2 (en) |
ES (1) | ES2224702T3 (en) |
ID (1) | ID29487A (en) |
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WO (1) | WO2000018853A1 (en) |
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- 1999-09-28 AU AU62712/99A patent/AU6271299A/en not_active Abandoned
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Cited By (16)
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GB2399090B (en) * | 2003-01-31 | 2005-06-08 | Chevron Usa Inc | High purity olefinic naphthas for the production of ethylene and propylene |
GB2408747B (en) * | 2003-01-31 | 2006-01-18 | Chevron Usa Inc | High purity olefinic naphthas for the production of ethylene and propylene |
US7150821B2 (en) | 2003-01-31 | 2006-12-19 | Chevron U.S.A. Inc. | High purity olefinic naphthas for the production of ethylene and propylene |
US7431821B2 (en) | 2003-01-31 | 2008-10-07 | Chevron U.S.A. Inc. | High purity olefinic naphthas for the production of ethylene and propylene |
GB2408747A (en) * | 2003-01-31 | 2005-06-08 | Chevron Usa Inc | Process for production of lower olefins |
US9809507B2 (en) | 2009-06-30 | 2017-11-07 | Jx Nippon Oil & Energy Corporation | Catalyst for producing monocyclic aromatic hydrocarbons, and method for producing monocyclic aromatic hydrocarbons |
US9815750B2 (en) | 2009-07-29 | 2017-11-14 | Jx Nippon Oil & Energy Corporation | Catalyst for producing monocyclic aromatic hydrocarbons, and method for producing monocyclic aromatic hydrocarbons |
US9433912B2 (en) | 2010-03-31 | 2016-09-06 | Indian Oil Corporation Limited | Process for simultaneous cracking of lighter and heavier hydrocarbon feed and system for the same |
WO2011121613A2 (en) | 2010-03-31 | 2011-10-06 | Indian Oil Corporation Ltd | A process for simultaneous cracking of lighter and heavier hydrocarbon feed and system for the same |
US9382484B2 (en) | 2010-12-28 | 2016-07-05 | Jx Nippon Oil & Energy Corporation | Production method of monocyclic aromatic hydrocarbons |
US9815047B2 (en) | 2010-12-28 | 2017-11-14 | Jx Nippon Oil & Energy Corporation | Catalyst for producing monocyclic aromatic hydrocarbon and production method of monocyclic aromatic hydrocarbon |
US8772192B2 (en) | 2012-06-29 | 2014-07-08 | Saudi Basic Industries Corporation | Germanium silicalite catalyst and method of preparation and use |
KR101600430B1 (en) | 2015-01-08 | 2016-03-07 | 한국화학연구원 | A direct method for preparing monocyclic aromatics and longer-chain olefin by using CO2-rich syngas |
US10208256B2 (en) | 2015-01-08 | 2019-02-19 | Korea Research Institute Of Chemical Technology | Method for preparing monocyclic aromatic compounds and long-chain olefin compounds from carbon dioxide-rich synthesis gas |
KR20190136422A (en) | 2018-05-30 | 2019-12-10 | 한국화학연구원 | Fischer―Tropsch Catalysts for Preparing Long Chain Olefin and Method for Preparing Long Chain Olefin Using the Same |
KR20210111580A (en) | 2020-03-03 | 2021-09-13 | 한국화학연구원 | Catalysts for Preparing Linear Alpha Olefin by Using CO2―Rich Syngas and Method for Preparing Linear Alpha Olefin Using the Same |
Also Published As
Publication number | Publication date |
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DE69918451T2 (en) | 2005-07-28 |
NO20011561L (en) | 2001-03-27 |
US6548725B2 (en) | 2003-04-15 |
DE69918451D1 (en) | 2004-08-05 |
ID29487A (en) | 2001-08-30 |
AU6271299A (en) | 2000-04-17 |
JP2002525380A (en) | 2002-08-13 |
NO20011561D0 (en) | 2001-03-27 |
ATE270318T1 (en) | 2004-07-15 |
EP1117750A1 (en) | 2001-07-25 |
US20010056217A1 (en) | 2001-12-27 |
CA2345308A1 (en) | 2000-04-06 |
ES2224702T3 (en) | 2005-03-01 |
CN1320148A (en) | 2001-10-31 |
CN1195714C (en) | 2005-04-06 |
EP1117750B1 (en) | 2004-06-30 |
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