WO2017216616A1 - A fluid catalytic cracking process for obtaining cracked run naphtha from vacuum gas oil - Google Patents

A fluid catalytic cracking process for obtaining cracked run naphtha from vacuum gas oil Download PDF

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WO2017216616A1
WO2017216616A1 PCT/IB2016/053652 IB2016053652W WO2017216616A1 WO 2017216616 A1 WO2017216616 A1 WO 2017216616A1 IB 2016053652 W IB2016053652 W IB 2016053652W WO 2017216616 A1 WO2017216616 A1 WO 2017216616A1
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Prior art keywords
rare earth
earth metal
additive
catalyst composition
gas oil
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PCT/IB2016/053652
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French (fr)
Inventor
Raman Ravishankar
Sunil Mehla
Peddy Venkat CHALAPATHI RAO
Venkateswarlu Choudary Nettem
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Hindustan Petroleum Corporation Limited
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Publication of WO2017216616A1 publication Critical patent/WO2017216616A1/en

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C7/00—Purification; Separation; Use of additives
    • C07C7/10—Purification; Separation; Use of additives by extraction, i.e. purification or separation of liquid hydrocarbons with the aid of liquids
    • 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
    • B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
    • B01J37/28—Phosphorising
    • 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
    • B01J29/65—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of the ferrierite type, e.g. types ZSM-21, ZSM-35 or ZSM-38, as exemplified by patent documents US4046859, US4016245 and US4046859, respectively
    • B01J29/655—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of the ferrierite type, e.g. types ZSM-21, ZSM-35 or ZSM-38, as exemplified by patent documents US4046859, US4016245 and US4046859, respectively containing rare earth elements, titanium, zirconium, hafnium, zinc, cadmium, mercury, gallium, indium, thallium, tin or lead
    • 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
    • B01J29/80—Mixtures of different zeolites
    • 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
    • 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
    • B01J2229/18—After treatment, characterised by the effect to be obtained to introduce other elements into or onto the molecular sieve itself
    • B01J2229/186—After treatment, characterised by the effect to be obtained to introduce other elements into or onto the molecular sieve itself not in framework positions

Definitions

  • the present disclosure relates to a fluid catalytic cracking process for obtaining cracked run naphtha from vacuum gas oil.
  • Vacuum distillation of crude oil results in a variety of petroleum products with a wide range of molecular weights.
  • the heavier hydrocarbon fractions, usually, the left-overs from vacuum distillation process are converted and refined into more valuable lower molecular weight hydrocarbons with the help of a fluid catalytic cracking (FCC) unit.
  • FCC fluid catalytic cracking
  • the ever-increasing demand for gasoline has seen a surge in such refining units.
  • Vacuum Gas Oil (VGO) particularly comprising higher molecular weight or heavy hydrocarbons, is subjected to a fluid catalytic cracking (FCC) process, in an FCC unit, thereby producing or obtaining cracked run naphtha (CRN), fuel oil and offgas as the end- products.
  • FCC fluid catalytic cracking
  • the cracked run naphtha contains around 45-55% liquid olefins.
  • these liquid olefins come in contact with dissolved oxygen, they form hydro-peroxides as immediate products, which undergo further reactions to form insoluble oxidized species.
  • These oxidized species include peroxides, aldehydes, acids, ketones, and components having a molecular weight in the range of 200-600 g/mol (are commonly referred to as gum).
  • This insoluble gum formation in the interior of the process units results in fouling.
  • rigorous exclusion of oxygen or the addition of anti-oxidants are enough to eliminate fouling, in some industrial situations oxygen ingress cannot be easily prevented. If the liquid olefin content in the CRN is brought down, the gum formation and hence, fouling can be controlled.
  • An object of the present disclosure is to provide an FCC process to produce cracked run naphtha with low olefin content.
  • the present disclosure envisages a fluid catalytic cracking process for obtaining cracked run naphtha from vacuum gas oil.
  • Vacuum gas oil is subjected to the fluid catalytic cracking (FCC) process in the presence of a catalyst composition, which comprises an FCC catalyst (ECAT) and an additive, to obtain a resultant product containing cracked run naphtha with liquid olefinic content less than 40 wt%.
  • FCC fluid catalytic cracking
  • the additive comprises a zeolite and a rare earth metal promoter.
  • the zeolite can be one of ferrierite and/or ZSM-35.
  • the rare earth metal promoter can be one of lanthanum (La), zinc (Zn), and gallium (Ga).
  • the disclosure relates to a fluid catalytic cracking (FCC) process for obtaining cracked run naphtha with low olefin content.
  • FCC fluid catalytic cracking
  • the disclosure relates to a process that makes use of a catalyst composition comprising an FCC catalyst (ECAT) and an additive.
  • the additive comprises a zeolite and a rare earth metal promoter.
  • the FCC catalyst can be present in an amount in the range of 80 wt% to 93 wt% of the catalyst composition.
  • the additive can be present in an amount in the range of 7 wt% to 15 wt% of the catalyst composition.
  • the zeolite can be one of ferrierite and/or ZSM-35.
  • the rare earth metal promoter can be one of lanthanum (La), zinc (Zn), and gallium (Ga).
  • the precursor for the rare earth metal promoter can be a salt of the rare earth metal.
  • the precursor of the rare earth metal promoter is a nitrate salt of the rare earth metal promoter.
  • the catalyst composition can be prepared in the steps described herein below.
  • the zeolite having Si/Al molar ratio of 20 is loaded with one of the rare earth metal promoters.
  • a nitrate salt of one of the rare earth metal promoter is used as the precursor.
  • a pre-determined amount of the nitrate salt is dissolved in a pre-determined amount of water to obtain a metallic salt solution.
  • a pre-determined amount of the zeolite is added to the metallic salt solution to obtain a slurry.
  • the slurry is agitated at a temperature in the range of 70°C to 80°C and for a time period in the range of 2 hours to 3 hours, to allow the rare earth metal promoter to impregnate into the zeolite to obtain a rare earth metal promoter impregnated zeolite slurry.
  • the rare earth metal promoter impregnated zeolite slurry is further evaporated in a rotary evaporator maintained at a temperature in the range of 70°C to 80°C under vacuum to obtain a dried mass which is calcined at a temperature in the range of 500°C to 600°C for a time period in the range of 3 hours to 6 hours to obtain a calcined mass.
  • the calcined mass is grounded into fine powder, pressed into wafers and sieved to obtain particles having particle sizes ranging from 650 ⁇ to 800 ⁇ (rare earth metal promoter impregnated ferrierite). These particles are mixed with ECAT to obtain the catalyst composition.
  • the catalyst composition comprises at least one phosphorus containing compound, which can be present in an amount in the range of 1 wt% to 4 wt% of the additive.
  • the phosphorus containing compound can be at least one selected from the group consisting of phosphoric acid, phosphates, phosphorous acid, phosphites, pyrophosphoric acid, pyrophosphate, polymeric phosphoric acid, polyphosphates, metaphosphoric acid, and metaphosphate.
  • a FCC unit which is a fixed bed down-flow reactor, is maintained at a pressure in the range of 1 atm to 2 atm and at a temperature in the range of 400°C to 700°C.
  • a feedstock vacuum gas oil
  • V.D.U vacuum distillation unit
  • WHSV weight hourly space velocity
  • An inert gas, particularly nitrogen, is selected as a carrier gas.
  • the feedstock is contacted with the catalyst composition, to obtain a resultant product containing cracked run naphtha having a liquid olefinic content less than 40 wt%.
  • the catalyst composition of the present disclosure facilitates in reducing the concentration of olefin in the cracked run naphtha prepared while processing the feedstock, particularly vacuum gas oil, in the FCC unit.
  • Example-1 A comparative example for FCC of VGO with 100% conventional catalyst - FCC equilibrated catalyst (ECAT) The FCC reaction was carried out using VGO as the feedstock. The reaction was carried out in a fixed bed down-flow reactor unit with a high pressure liquid gas separator. The reaction parameters are listed in Table 1.
  • the catalyst used was 100% FCC catalyst (ECAT).
  • Example- 1 The resultant products obtained in Example- 1 and their percentage composition are listed in Table-3.
  • Ferrierite with Si/Al molar ratio of 20 was loaded with individual rare earth metal promoters, viz., La, Zn, and Ga, as listed in Table-2.
  • the nitrate salts of the metals were used as the precursor. 1.186 g of metal salts were dissolved in 30 ml of water and made into their respective solutions. 10 g of ferrierite was added to this metallic salt solution to obtain a slurry. The slurry was agitated at 75 °C for 3 hours to allow the rare earth metal promoters to impregnate into ferrierite to obtain a rare earth metal promoter impregnated ferrierite slurry.
  • the rare earth metal promoter impregnated ferrierite slurry was evaporated in a rotary evaporator maintained at 75 °C under vacuum to obtain a dried mass which was calcined at 550°C for 5 hours to result in a calcined mass.
  • the calcined mass was ground into fine powder, pressed into wafers and sieved to obtain particles having particle sizes ranging from 650 ⁇ to 800 ⁇ (rare earth metal promoter impregnated ferrierite). These particles were mixed with ECAT to obtain a catalyst composition, which was used in the FCC process carried out in a manner similar to Example- 1.
  • the resultant products obtained in Examples 3- 6 and their percentage composition are listed in Table-3.
  • Table-3 The composition of the individual components of CRN from Examples 1-4.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Materials Engineering (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Analytical Chemistry (AREA)
  • Water Supply & Treatment (AREA)
  • Catalysts (AREA)

Abstract

The present disclosure relates to a fluid catalytic cracking process for obtaining cracked run naphtha from vacuum gas oil. The process is carried out in the presence of a catalyst composition comprising an FCC catalyst (ECAT) and an additive, to obtain cracked run naphtha with liquid olefinic content less than 40 wt%. The additive comprises a zeolite and a rare earth metal promoter. The zeolite is one of ferrierite and/or ZSM-35, and the rare earth metal promoter is one of lanthanum (La), zinc (Zn), and gallium (Ga).

Description

A FLUID CATALYTIC CRACKING PROCESS FOR OBTAINING CRACKED RUN NAPHTHA FROM VACUUM GAS OIL
FIELD
The present disclosure relates to a fluid catalytic cracking process for obtaining cracked run naphtha from vacuum gas oil.
BACKGROUND Vacuum distillation of crude oil results in a variety of petroleum products with a wide range of molecular weights. The heavier hydrocarbon fractions, usually, the left-overs from vacuum distillation process are converted and refined into more valuable lower molecular weight hydrocarbons with the help of a fluid catalytic cracking (FCC) unit. The ever-increasing demand for gasoline has seen a surge in such refining units. Vacuum Gas Oil (VGO), particularly comprising higher molecular weight or heavy hydrocarbons, is subjected to a fluid catalytic cracking (FCC) process, in an FCC unit, thereby producing or obtaining cracked run naphtha (CRN), fuel oil and offgas as the end- products. Typically, the cracked run naphtha (CRN) contains around 45-55% liquid olefins. When these liquid olefins come in contact with dissolved oxygen, they form hydro-peroxides as immediate products, which undergo further reactions to form insoluble oxidized species. These oxidized species include peroxides, aldehydes, acids, ketones, and components having a molecular weight in the range of 200-600 g/mol (are commonly referred to as gum). This insoluble gum formation in the interior of the process units results in fouling. Although, rigorous exclusion of oxygen or the addition of anti-oxidants are enough to eliminate fouling, in some industrial situations oxygen ingress cannot be easily prevented. If the liquid olefin content in the CRN is brought down, the gum formation and hence, fouling can be controlled.
Thus, a need to reduce the liquid olefin content in CRN arises. To meet this need, a separate hydrotreating unit for hydrogenation of olefins may be used. However such units increase the overall cost. Therefore, there is a need for an FCC process for the production of cracked run naphtha that overcomes the above-mentioned drawback. OBJECTS
Some of the objects of the present disclosure, which at least one embodiment herein satisfies, are as follows.
It is an object of the present disclosure to ameliorate one or more problems of the prior art or to at least provide a useful alternative.
An object of the present disclosure is to provide an FCC process to produce cracked run naphtha with low olefin content.
Other objects and advantages of the present disclosure will be more apparent from the following description, which is not intended to limit the scope of the present disclosure. SUMMARY
The present disclosure envisages a fluid catalytic cracking process for obtaining cracked run naphtha from vacuum gas oil.
Vacuum gas oil is subjected to the fluid catalytic cracking (FCC) process in the presence of a catalyst composition, which comprises an FCC catalyst (ECAT) and an additive, to obtain a resultant product containing cracked run naphtha with liquid olefinic content less than 40 wt%.
The additive comprises a zeolite and a rare earth metal promoter. The zeolite can be one of ferrierite and/or ZSM-35.
The rare earth metal promoter can be one of lanthanum (La), zinc (Zn), and gallium (Ga).
DETAILED DESCRIPTION
The disclosure relates to a fluid catalytic cracking (FCC) process for obtaining cracked run naphtha with low olefin content. In particular, the disclosure relates to a process that makes use of a catalyst composition comprising an FCC catalyst (ECAT) and an additive. The additive comprises a zeolite and a rare earth metal promoter. The FCC catalyst can be present in an amount in the range of 80 wt% to 93 wt% of the catalyst composition.
The additive can be present in an amount in the range of 7 wt% to 15 wt% of the catalyst composition. The zeolite can be one of ferrierite and/or ZSM-35.
The rare earth metal promoter can be one of lanthanum (La), zinc (Zn), and gallium (Ga).
The precursor for the rare earth metal promoter can be a salt of the rare earth metal.
In one embodiment of the present disclosure, the precursor of the rare earth metal promoter is a nitrate salt of the rare earth metal promoter. The catalyst composition can be prepared in the steps described herein below.
The zeolite having Si/Al molar ratio of 20 is loaded with one of the rare earth metal promoters. A nitrate salt of one of the rare earth metal promoter is used as the precursor. A pre-determined amount of the nitrate salt is dissolved in a pre-determined amount of water to obtain a metallic salt solution. A pre-determined amount of the zeolite is added to the metallic salt solution to obtain a slurry. The slurry is agitated at a temperature in the range of 70°C to 80°C and for a time period in the range of 2 hours to 3 hours, to allow the rare earth metal promoter to impregnate into the zeolite to obtain a rare earth metal promoter impregnated zeolite slurry. The rare earth metal promoter impregnated zeolite slurry is further evaporated in a rotary evaporator maintained at a temperature in the range of 70°C to 80°C under vacuum to obtain a dried mass which is calcined at a temperature in the range of 500°C to 600°C for a time period in the range of 3 hours to 6 hours to obtain a calcined mass. The calcined mass is grounded into fine powder, pressed into wafers and sieved to obtain particles having particle sizes ranging from 650 μπι to 800 μπι (rare earth metal promoter impregnated ferrierite). These particles are mixed with ECAT to obtain the catalyst composition. Additionally, the catalyst composition comprises at least one phosphorus containing compound, which can be present in an amount in the range of 1 wt% to 4 wt% of the additive.
The phosphorus containing compound can be at least one selected from the group consisting of phosphoric acid, phosphates, phosphorous acid, phosphites, pyrophosphoric acid, pyrophosphate, polymeric phosphoric acid, polyphosphates, metaphosphoric acid, and metaphosphate.
A FCC unit, which is a fixed bed down-flow reactor, is maintained at a pressure in the range of 1 atm to 2 atm and at a temperature in the range of 400°C to 700°C. A feedstock (vacuum gas oil), which is typically a left-over of a vacuum distillation unit (V.D.U), is introduced into the FCC unit at a rate of 12 ml/hr and at a weight hourly space velocity (WHSV) of 6 hr-1 to 10 hr"1. An inert gas, particularly nitrogen, is selected as a carrier gas. The feedstock is contacted with the catalyst composition, to obtain a resultant product containing cracked run naphtha having a liquid olefinic content less than 40 wt%. The catalyst composition of the present disclosure facilitates in reducing the concentration of olefin in the cracked run naphtha prepared while processing the feedstock, particularly vacuum gas oil, in the FCC unit.
The present disclosure is further described in light of the following experiments which are set forth for illustration purpose only and not to be construed for limiting the scope of the disclosure. The following laboratory scale experiments can be scaled up to industrial/commercial scale:
EXAMPLES
Example-1: A comparative example for FCC of VGO with 100% conventional catalyst - FCC equilibrated catalyst (ECAT) The FCC reaction was carried out using VGO as the feedstock. The reaction was carried out in a fixed bed down-flow reactor unit with a high pressure liquid gas separator. The reaction parameters are listed in Table 1.
The catalyst used was 100% FCC catalyst (ECAT).
Table-1: FCC Reaction Parameters
Figure imgf000005_0001
The resultant products obtained in Example- 1 and their percentage composition are listed in Table-3.
Examples 2-4: FCC of VGO with 85 wt% FCC catalyst (ECAT) and 15 wt% additive
Ferrierite with Si/Al molar ratio of 20 was loaded with individual rare earth metal promoters, viz., La, Zn, and Ga, as listed in Table-2. The nitrate salts of the metals were used as the precursor. 1.186 g of metal salts were dissolved in 30 ml of water and made into their respective solutions. 10 g of ferrierite was added to this metallic salt solution to obtain a slurry. The slurry was agitated at 75 °C for 3 hours to allow the rare earth metal promoters to impregnate into ferrierite to obtain a rare earth metal promoter impregnated ferrierite slurry. The rare earth metal promoter impregnated ferrierite slurry was evaporated in a rotary evaporator maintained at 75 °C under vacuum to obtain a dried mass which was calcined at 550°C for 5 hours to result in a calcined mass. The calcined mass was ground into fine powder, pressed into wafers and sieved to obtain particles having particle sizes ranging from 650 μπι to 800 μπι (rare earth metal promoter impregnated ferrierite). These particles were mixed with ECAT to obtain a catalyst composition, which was used in the FCC process carried out in a manner similar to Example- 1. The resultant products obtained in Examples 3- 6 and their percentage composition are listed in Table-3.
Table-2: Catalyst compositions used in Examples 2-4 with their metal loadings
Figure imgf000006_0001
Table-3: The composition of the individual components of CRN from Examples 1-4.
Figure imgf000006_0002
% Olefin 0 21.68 62.42 53.63 50.04
Reduction
From Table-3, it is evident that using the catalyst composition prepared in Examples 2-4, the olefins content in the CRN is reduced as compared to that present in the feed-stock.
TECHNICAL ADVANCES AND ECONOMICAL SIGNIFICANCE
The present disclosure described herein above has several technical advantages including, but not limited to, the realization of a fluid catalytic cracking (FCC) process that:
- provides cracked run naphtha with low olefin content.
The foregoing description of the specific embodiments so fully reveal the general nature of the embodiments herein that others can, by applying current knowledge, readily modify and/or adapt for various applications such specific embodiments without departing from the generic concept, and, therefore, such adaptations and modifications should and are intended to be comprehended within the meaning and range of equivalents of the disclosed embodiments. It is to be understood that the phraseology or terminology employed herein is for the purpose of description and not of limitation. Therefore, while the embodiments herein have been described in terms of preferred embodiments, those skilled in the art will recognize that the embodiments herein can be practiced with modification within the spirit and scope of the embodiments as described herein.
Throughout this specification the word "comprise", or variations such as "comprises" or "comprising", should be understood to imply the inclusion of a stated element, integer or step, or group of elements, integers or steps, but not the exclusion of any other element, integer or step, or group of elements, integers or steps.
The use of the expression "at least" or "at least one" suggests the use of one or more elements or ingredients or quantities, as the use may be in the embodiment of the disclosure to achieve one or more of the desired objects or results.
Any discussion of documents, acts, materials, devices, articles or the like that has been included in this specification is solely for the purpose of providing a context for the disclosure. It is not to be taken as an admission that any or all of these matters form a part of the prior art base or were common general knowledge in the field relevant to the disclosure as it existed anywhere before the priority date of this application. The numerical values mentioned for the various physical parameters, dimensions or quantities are only approximations and it is envisaged that the values higher/lower than the numerical values assigned to the parameters, dimensions or quantities fall within the scope of the disclosure, unless there is a statement in the specification specific to the contrary. While considerable emphasis has been placed herein on the components and component parts of the preferred embodiments, it will be appreciated that many embodiments can be made and that many changes can be made in the preferred embodiments without departing from the principles of the disclosure. These and other changes in the preferred embodiment as well as other embodiments of the disclosure will be apparent to those skilled in the art from the disclosure herein, whereby it is to be distinctly understood that the foregoing descriptive matter is to be interpreted merely as illustrative of the disclosure and not as a limitation.

Claims

CLAIMS:
A fluid catalytic cracking (FCC) process for obtaining cracked run naphtha from vacuum gas oil, said process comprising treating the vacuum gas oil in a reactor maintained at a temperature ranging from 400°C to 750°C and at a pressure ranging from 1 atm to 2 atm, in the presence of a catalyst composition, wherein said catalyst composition comprises an FCC catalyst (ECAT) and an additive, said additive comprising a zeolite and a rare earth metal promoter, said zeolite is one of ferrierite and ZSM-35, and said rare earth metal promoter is one of lanthanum (La), zinc (Zn), and gallium (Ga), to obtain a resultant product containing cracked run naphtha with liquid olefinic content less than 40 wt%.
2. The process as claimed in claim 1, wherein said FCC catalyst in said catalyst composition is in the range of 85 wt% to 93 wt , and said additive in said catalyst composition is in the range of 7 wt% to 15 wt%.
3. The process as claimed in claim 1, wherein said rare earth metal promoter in said additive is in the range of 1 wt% to 10 wt% of said additive.
4. The process as claimed in claim 1, wherein the precursor for said rare earth metal promoter is a nitrate salt of said rare earth metal.
5. The process as claimed in claim 1, wherein the vacuum gas oil is introduced into the reactor at a weight hourly space velocity ranging from 6 hr-1 to 10 hr 1.
6. The process as claimed in claim 1, wherein said catalyst composition comprises at least one phosphorus containing compound, said at least one phosphorus containing compound is selected from the group consisting of phosphoric acid, phosphates, phosphorous acid, phosphites, pyrophosphoric acid, pyrophosphate, polymeric phosphoric acid, polyphosphates, metaphosphoric acid, and metaphosphate.
7. The process as claimed in claim 6, wherein said at least one phosphorus containing compound is present in an amount in the range of 1 wt% to 4 wt% of said additive.
PCT/IB2016/053652 2016-06-15 2016-06-20 A fluid catalytic cracking process for obtaining cracked run naphtha from vacuum gas oil WO2017216616A1 (en)

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Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4927526A (en) * 1984-07-05 1990-05-22 Mobil Oil Corporation Octane improvement of gasoline in catalytic cracking without decreasing total liquid yield
US20040152586A1 (en) * 2003-02-05 2004-08-05 Ou John Di-Yi Combined cracking and selective hydrogen combustion for catalytic cracking
US6797155B1 (en) * 1999-12-21 2004-09-28 Exxonmobil Research & Engineering Co. Catalytic cracking process using a modified mesoporous aluminophosphate material
US20080156696A1 (en) * 2006-12-29 2008-07-03 Niccum Phillip K FCC process for converting C3/C4 feeds to olefins and aromatics
US20120289752A1 (en) * 2011-04-21 2012-11-15 Shell Oil Company Process for converting a solid biomass material

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4927526A (en) * 1984-07-05 1990-05-22 Mobil Oil Corporation Octane improvement of gasoline in catalytic cracking without decreasing total liquid yield
US6797155B1 (en) * 1999-12-21 2004-09-28 Exxonmobil Research & Engineering Co. Catalytic cracking process using a modified mesoporous aluminophosphate material
US20040152586A1 (en) * 2003-02-05 2004-08-05 Ou John Di-Yi Combined cracking and selective hydrogen combustion for catalytic cracking
US20080156696A1 (en) * 2006-12-29 2008-07-03 Niccum Phillip K FCC process for converting C3/C4 feeds to olefins and aromatics
US20120289752A1 (en) * 2011-04-21 2012-11-15 Shell Oil Company Process for converting a solid biomass material

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