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WO2001064761A2 - Procede de production de polypropylene a partir d'olefines c3 produites selectivement dans un processus de craquage catalytique fluide a partir d'une alimentation en naphta/vapeur - Google Patents

Procede de production de polypropylene a partir d'olefines c3 produites selectivement dans un processus de craquage catalytique fluide a partir d'une alimentation en naphta/vapeur Download PDF

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Publication number
WO2001064761A2
WO2001064761A2 PCT/US2001/006685 US0106685W WO0164761A2 WO 2001064761 A2 WO2001064761 A2 WO 2001064761A2 US 0106685 W US0106685 W US 0106685W WO 0164761 A2 WO0164761 A2 WO 0164761A2
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WO
WIPO (PCT)
Prior art keywords
naphtha
products
propylene
olefins
feed
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/US2001/006685
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English (en)
Other versions
WO2001064761A3 (fr
Inventor
Shun C. Fung
Tan-Jen Chen
Marcel J. Janssen
William A. Wachter
B. Erik Henry
John E. Asplin
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
ExxonMobil Chemical Patents Inc
Original Assignee
ExxonMobil Chemical Patents Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from US09/517,554 external-priority patent/US6388152B1/en
Priority claimed from US09/517,497 external-priority patent/US6258990B1/en
Priority claimed from US09/517,551 external-priority patent/US6258257B1/en
Priority claimed from US09/517,503 external-priority patent/US6339180B1/en
Priority to JP2001564253A priority Critical patent/JP2004516335A/ja
Priority to AU2001239990A priority patent/AU2001239990A1/en
Priority to EP01914623A priority patent/EP1261649A2/fr
Application filed by ExxonMobil Chemical Patents Inc filed Critical ExxonMobil Chemical Patents Inc
Priority to MXPA02008554A priority patent/MXPA02008554A/es
Priority to CA002400382A priority patent/CA2400382A1/fr
Publication of WO2001064761A2 publication Critical patent/WO2001064761A2/fr
Publication of WO2001064761A3 publication Critical patent/WO2001064761A3/fr
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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Classifications

    • 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
    • C10G57/00—Treatment of hydrocarbon oils, in the absence of hydrogen, by at least one cracking process or refining process and at least one other conversion process
    • C10G57/02—Treatment of hydrocarbon oils, in the absence of hydrogen, by at least one cracking process or refining process and at least one other conversion process with polymerisation
    • 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
    • C10G51/00—Treatment of hydrocarbon oils, in the absence of hydrogen, by two or more cracking processes only
    • C10G51/02—Treatment of hydrocarbon oils, in the absence of hydrogen, by two or more cracking processes only plural serial stages only
    • C10G51/026—Treatment of hydrocarbon oils, in the absence of hydrogen, by two or more cracking processes only plural serial stages only only catalytic cracking steps
    • 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

Definitions

  • the present invention relates to a process for producing polypropylene from C 3 olefins selectively produced from a catalytically cracked or thermally cracked naphtha stream.
  • a problem inherent in producing olefin products using FCC units is that the process depends on a specific catalyst balance to maximize production of light olefins while also achieving high conversion of the 650° F + (340° C +) feed components.
  • olefin selectivity is generally low because of undesirable side reactions, such as cracking, isomerization, aromatization and hydrogen transfer reactions. Light saturated gases produced from undesirable side reactions result in increased costs to recover the desirable light olefins. Therefore, it is desirable to maximize olefin production in a process that allows a high degree of control over the selectivity to C 2 - C 4 olefins.
  • One embodiment of the present invention is a process for producing polypropylene comprising the steps of (a) feeding steam and a naphtha feed containing less than about 40 wt.% paraffins and between about 15 and about 70 wt.% olefins into a reaction zone; (b) contacting the naphtha feed with a catalyst comprising a crystalline zeolite having an average pore diameter less than about 0.7 nm at conditions including a temperature from about 500° to 650° C, a hydrocarbon partial pressure of 10 to 40 psia, a hydrocarbon residence time of 1 to 10 seconds, and a catalyst to feed weight ratio of about 4 to about 10, wherein no more than about 20 wt.% of paraffins are converted to olefins, wherein polypropylene comprises at least about 90 mol.% of the total C 3 products; and, (c) separating the propylene from the C 3 products and polymerizing the propylene to form polypropylene.
  • the crystalline zeolite is selected from the ZSM series.
  • the catalyst is a ZSM-5 type catalyst.
  • the feedstock contains about 5 to 35 wt.% paraffins, and from about 20 to 70 wt.% olefins.
  • reaction zone is operated at a temperature from about 525° C to about 600° C.
  • Feeds that are suitable for producing the relatively high C 2 , C 3 , and C 4 olefin yields are streams boiling in the naphtha range and containing less than about 40 wt.%, preferably from about 5 wt.% to about 35 wt.%, more preferably from about 10 wt.% to about 30 wt.%, and most preferably from about 10 to 25 wt.%) paraffins, and from about 15 wt.%, preferably from about 20 wt.% to about 70 wt.% olefins.
  • the feed may also contain naphthenes and aromatics.
  • Naphtha boiling range streams are typically those having a boiling range from about 65° F to about 430° F (18-225° C), preferably from about 65° F to about 300° F (18- 150° C).
  • the naphtha feed may be a thermally-cracked or a catalytically-cracked naphtha derived from any appropriate source.
  • the naphtha streams may derive from the fluid catalytic cracking (FCC) of gas oils and resids or from delayed- or fluid-coking of resids.
  • the naphtha streams used in the present invention derive from the fluid catalytic cracking of gas oils and resids because these naphthas are typically rich in olefins and/or diolefins and relatively lean in paraffins.
  • the process of the present invention is performed in a process unit comprising a reaction zone, a stripping zone, a catalyst regeneration zone, and a fractionation zone.
  • the naphtha feed is fed into the reaction zone as a mixture of naphtha and steam, where it contacts a source of hot, regenerated catalyst.
  • the hot catalyst vaporizes and cracks the feed at a temperature from about 500° C to 650° C, preferably from about 525° C to 600° C.
  • the cracking reaction deposits coke on the catalyst, thereby deactivating the catalyst.
  • the cracked products are separated from the coked catalyst and sent to a fractionator.
  • the coked catalyst is passed through the stripping zone where volatiles are stripped from the catalyst particles with a stripping medium such as steam.
  • the stripping can be performed under low severity conditions to retain a greater fraction of adsorbed hydrocarbons for heat balance.
  • the stripped catalyst is then passed to the regeneration zone where it is regenerated by burning at least a portion of the coke on the catalyst in the presence of an oxygen containing gas, preferably air. Decoking restores catalyst activity and simultaneously heats the catalyst to between 650° C and 750° C.
  • the hot regenerated catalyst is then recycled to the reaction zone to react with fresh naphtha feed. Flue gas formed by burning coke in the regenerator may be treated for removal of parti culates and for conversion of carbon monoxide.
  • the cracked products from the reaction zone are sent to a fractionation zone where various products are recovered, particularly a C 3 fraction, a C 4 fraction rich in olefins, and a C 5 fraction rich in olefins.
  • the amount of steam co-fed with the naphtha feed will typically be in the range of about 10 to 250 mol.%, preferably from about 25 to 150 mol.% steam to naphtha.
  • the reaction zone is operated at process conditions that will maximize C 2 to C olefin (particularly propylene) selectivity with relatively high conversion of C 5 + olefins.
  • Catalysts suitable for use in the practice of the present invention are those comprising a crystalline zeolite having an average pore diameter less than about 0.7 nanometers (nm), said crystalline zeolite comprising from about 10 wt.%» to about 50 wt.% of the total fluidized catalyst composition.
  • the crystalline zeolite be selected from the family of medium-pore-size ( ⁇ 0.7 nm) crystalline aluminosilicates, otherwise referred to as zeolites.
  • zeolites are the medium-pore zeolites with a silica to alumina molar ratio of less than about 75: 1, preferably less than about 50: 1, and more preferably less than about 40:1, although some embodiments may have silica to alumina ratios greater than 40: 1.
  • the pore diameter also referred to as effective pore diameter, is measured using standard adsorption techniques and hydrocarbonaceous compounds of known minimum kinetic diameters. See Breck, Zeolite Molecular Sieves, 1974 and Anderson et al., J. Catalysis 58, 114 (1979), both of which are incorporated herein by reference.
  • Medium-pore-size zeolites that can be used in the practice of the present invention are described in "Atlas of Zeolite Structure Types," eds. W. H. Meier and D. H. Olson, Butterworth-Heineman, Third Edition, 1992, which is hereby incorporated by reference.
  • the medium-pore-size zeolites generally have a pore size from about 5A, to about 7A and include for example, MFI, MFS, MEL, MTW, EUO, MTT, HEU, FER, and TON structure type zeolites (IUPAC Commission of Zeolite Nomenclature).
  • Non-limiting examples of such medium- pore-size zeolites include ZSM-5, ZSM-12, ZSM-22, ZSM-23, ZSM-34, ZSM- 35, ZSM-38, ZSM-48, ZSM-50, silicalite, and silicalite 2.
  • ZSM-5 which is described in U.S. Patent Nos. 3,702,886 and 3,770,614.
  • ZSM- 11 is described in U.S. Patent No. 3,709,979; ZSM-12 in U.S. Patent No. 3,832,449; ZSM-21 and ZSM-38 in U.S. Patent No. 3,948,758; ZSM-23 in U.S. Patent No. 4,076,842; and ZSM-35 in U.S. Patent No.
  • Suitable medium- pore-size zeolites include the silicoaluminophosphates (SAPO), such as SAPO-4 and SAPO-11 which is described in U.S. Patent No. 4,440,871 ; chromosilicates; gallium silicates; iron silicates; aluminum phosphates (ALPO), such as ALPO- 11 described in U.S. Patent No. 4,310,440; titanium aluminosilicates (TASO), such as TASO-45 described in EP-A No. 229,295; boron silicates, described in U.S. Patent No. 4,254,297; titanium aluminophosphates (TAPO), such as TAPO- 11 described in U.S. Patent No. 4,500,651; and iron aluminosilicates.
  • SAPO silicoaluminophosphates
  • SAPO-4 and SAPO-11 which is described in U.S. Patent No. 4,440,871
  • chromosilicates such as ALPO
  • the medium-pore-size zeolites can include "crystalline admixtures" that are thought to be the result of faults occurring within the crystal or crystalline area during the synthesis of the zeolites.
  • Examples of crystalline admixtures of ZSM-5 and ZSM-11 are disclosed in U.S. Patent No. 4,229,424 which is incorporated herein by reference.
  • the crystalline admixtures are themselves medium-pore-size zeolites and are not to be confused with physical admixtures of zeolites in which distinct crystals of crystallites of different zeolites are physically present in the same catalyst composite or hydrothermal reaction mixtures.
  • the catalysts of the present invention are held together with an inorganic oxide matrix material component.
  • the inorganic oxide matrix component binds the catalyst components together so that the catalyst product is hard enough to survive interparticle and reactor wall collisions.
  • the inorganic oxide matrix can be made from an inorganic oxide sol or gel that is dried to "bind" the catalyst components together.
  • the inorganic oxide matrix is not catalytically active and will comprise oxides of silicon and aluminum. It is also preferred that separate alumina phases be incorporated into the inorganic oxide matrix.
  • Species of aluminum oxyhydroxides- ⁇ -alumina, boehmite, diaspore, and transitional aluminas such as ⁇ -alumina, ⁇ -alumina, ⁇ -alumina, ⁇ -alumina, ⁇ -alumina, K- alumina, and p-alumina can be employed.
  • the alumina species is an aluminum trihydroxide such as gibbsite, bayerite, nordstrandite, or doyelite.
  • the matrix material may also contain phosphorous or aluminum phosphate.
  • Preferred process conditions include temperatures from about 500° C to about 650° C, preferably from about 500° C to 600° C; hydrocarbon partial pressures from about 10 to 40 psia (70-280 kPa), preferably from about 20 to 35 psia (140-245 kPa); and a catalyst to naphtha (wt/wt) ratio from about 3 to 12, preferably from about 4 to 10, where catalyst weight is total weight of the catalyst composite.
  • the naphtha residence time in the reaction zone is less than about 10 seconds, for example from about 1 to 10 seconds.
  • the reaction conditions will be such that at least about 60 wt.% of the C 5 + olefins in the naphtha stream are converted to C - products and less than about 25 wt.%, preferably less than about 20 wt.% of the paraffins are converted to C 4 - products, and that propylene comprises at least about 90 mol.%, preferably greater than about 95 mol.% of the total C 3 reaction products with the weight ratio of propylene/total C 2 - products greater than about 3.5.
  • ethylene comprises at least about 90 mol.% of the C 2 products, with the weight ratio of propylene:ethylene being greater than about 4, and that the "full range" C 5 + product is enhanced in both motor and research octanes relative to the naphtha feed. It is within the scope of this invention to pre-coke the catalysts before introducing the feed to further improve the selectivity to propylene. It is also within the scope of this invention to feed an effective amount of single ring aromatics to the reaction zone to improve the selectivity of propylene versus ethylene.
  • the aromatics may be from an external source such as a reforming process unit or they may consist of heavy naphtha recycle product from the instant process.
  • Example 1 shows that increasing Cat/Oil ratio improves propylene yield, but sacrifices propylene purity.
  • Comparison of Examples 3 and 4 and 5 and 6 shows reducing oil partial pressure greatly improves propylene purity without compromising propylene yield.
  • Comparison of Examples 7 and 8 and 9 and 10 shows increasing temperature improves both propylene yield and purity.
  • Comparison of Examples 11 and 12 shows decreasing cat residence time improves propylene yield and purity.
  • Example 13 shows an example where both high propylene yield and purity are obtained at a reactor temperature and cat/oil ratio that can be achieved using a conventional FCC reactor/regenerator design for the second stage.
  • the cracking of olefins and paraffins contained in naphtha streams can produce significant amounts of ethylene and propylene.
  • the selectivity to ethylene or propylene and selectivity of propylene to propane varies as a function of catalyst and process operating conditions. It has been found that propylene yield can be increased by co-feeding steam along with cat naphtha to the reactor.
  • the catalyst may be ZSM-5 or other small or medium-pore zeolites.
  • Table 2 illustrates the increase in propylene yield when 5 wt.% steam is co-fed with a cat naphtha containing 38.8 wt% olefins. Although propylene yield increased, the propylene purity is diminished. Thus, other operating conditions may need to be adjusted to maintain the targeted propylene selectivity.
  • Light olefins resulting from the preferred process may be used as feeds for processes such as oligomerization, polymerization, co-polymerization, ter- polymerization, and related processes (hereinafter "polymerization") to form macromolecules.
  • Such light olefins may be polymerized both alone and in combination with other species, in accordance with polymerization methods known in the art. In some cases it may be desirable to separate, concentrate, purify, upgrade, or otherwise process the light olefins prior to polymerization.
  • Propylene and ethylene are preferred polymerization feeds. Polypropylene and polyethylene are preferred polymerization products made therefrom.

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  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Polymerisation Methods In General (AREA)
  • Polymerization Catalysts (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
  • Catalysts (AREA)

Abstract

L'invention concerne un procédé de production de polymères à partir d'oléfines C2-C4 produites sélectivement à partir d'un flux de naphta craqué par voie catalytique ou thermique. Un mélange de flux de naphta et d'un flux de vapeur est acheminé dans une zone de réaction dans laquelle il est mis au contact avec un catalyseur contenant environ 10 à 50 % en poids d'une zéolite cristalline ayant un diamètre de pore moyen inférieur à environ 0,7 nanomètre, dans des conditions de réaction comprenant des températures allant d'environ 500 °C à 650 °C, et une pression partielle d'hydrocarbures allant d'environ 10 à 40 psia.
PCT/US2001/006685 2000-03-02 2001-03-01 Procede de production de polypropylene a partir d'olefines c3 produites selectivement dans un processus de craquage catalytique fluide a partir d'une alimentation en naphta/vapeur Ceased WO2001064761A2 (fr)

Priority Applications (5)

Application Number Priority Date Filing Date Title
CA002400382A CA2400382A1 (fr) 2000-03-02 2001-03-01 Procede de production de polypropylene a partir d'olefines c3 produites selectivement dans un processus de craquage catalytique fluide a partir d'une alimentation en naphta/vapeur
MXPA02008554A MXPA02008554A (es) 2000-03-02 2001-03-01 Proceso para producir polipropileno a partir de olefinas c3 producidas de manera selectiva en un proceso de desintegracion catalitica fluida a partir de una alimentacion de nafta/vapor de agua.
JP2001564253A JP2004516335A (ja) 2000-03-02 2001-03-01 流動接触分解プロセスにおけるナフサ／スチーム供給物から選択的に製造されるｃ３オレフィンからポリプロピレンを製造する方法
EP01914623A EP1261649A2 (fr) 2000-03-02 2001-03-01 Procede de production de polypropylene a partir d'olefines c 3? produites selectivement dans un processus de craquage catalytique fluide a partir d'une alimentation en naphta/vapeur
AU2001239990A AU2001239990A1 (en) 2000-03-02 2001-03-01 Process for producing polypropylene from C3 olefins selectively produced in a fluid catalytic cracking process from a naphtha/steam feed

Applications Claiming Priority (8)

Application Number Priority Date Filing Date Title
US09/517,554 2000-03-02
US09/517,554 US6388152B1 (en) 1998-05-05 2000-03-02 Process for producing polypropylene from C3 olefins selectively produced in a fluid catalytic cracking process
US09/517,503 2000-03-02
US09/517,503 US6339180B1 (en) 1998-05-05 2000-03-02 Process for producing polypropylene from C3 olefins selectively produced in a fluid catalytic cracking process
US09/517,551 US6258257B1 (en) 1998-05-05 2000-03-02 Process for producing polypropylene from C3 olefins selectively produced by a two stage fluid catalytic cracking process
US09/517,497 2000-03-02
US09/517,497 US6258990B1 (en) 1998-05-05 2000-03-02 Process for producing polypropylene from C3 olefins selectively produced in a fluid catalytic cracking process from a naphtha/steam feed
US09/517,551 2000-03-02

Publications (2)

Publication Number Publication Date
WO2001064761A2 true WO2001064761A2 (fr) 2001-09-07
WO2001064761A3 WO2001064761A3 (fr) 2002-01-03

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Family Applications (4)

Application Number Title Priority Date Filing Date
PCT/US2001/006685 Ceased WO2001064761A2 (fr) 2000-03-02 2001-03-01 Procede de production de polypropylene a partir d'olefines c3 produites selectivement dans un processus de craquage catalytique fluide a partir d'une alimentation en naphta/vapeur
PCT/US2001/006686 Ceased WO2001064762A2 (fr) 2000-03-02 2001-03-01 Procede de production de polypropylene a partir d'olefines c3 produites selectivement par un procede de craquage catalytique fluide a deux niveaux
PCT/US2001/006684 Ceased WO2001064760A2 (fr) 2000-03-02 2001-03-01 Procede de production de polypropylene a partir d'olefines c3 produites selectivement dans un processus de craquage catalytique fluide
PCT/US2001/006687 Ceased WO2001064763A2 (fr) 2000-03-02 2001-03-01 Procede de production de polypropylene a partir d'olefines c3 produites selectivement dans un procede de craquage catalytique fluide

Family Applications After (3)

Application Number Title Priority Date Filing Date
PCT/US2001/006686 Ceased WO2001064762A2 (fr) 2000-03-02 2001-03-01 Procede de production de polypropylene a partir d'olefines c3 produites selectivement par un procede de craquage catalytique fluide a deux niveaux
PCT/US2001/006684 Ceased WO2001064760A2 (fr) 2000-03-02 2001-03-01 Procede de production de polypropylene a partir d'olefines c3 produites selectivement dans un processus de craquage catalytique fluide
PCT/US2001/006687 Ceased WO2001064763A2 (fr) 2000-03-02 2001-03-01 Procede de production de polypropylene a partir d'olefines c3 produites selectivement dans un procede de craquage catalytique fluide

Country Status (7)

Country Link
EP (3) EP1261648A2 (fr)
JP (3) JP2003525323A (fr)
CN (3) CN1406252A (fr)
AU (4) AU2001243379A1 (fr)
CA (3) CA2400382A1 (fr)
MX (3) MXPA02008554A (fr)
WO (4) WO2001064761A2 (fr)

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WO2012088852A1 (fr) 2010-12-28 2012-07-05 中国科学院大连化学物理研究所 Procédé pour le craquage catalytique d'un naphta couplé à du méthanol utilisant un catalyseur à tamis moléculaire zsm-5 modifié

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US7270739B2 (en) 2003-02-28 2007-09-18 Exxonmobil Research And Engineering Company Fractionating and further cracking a C6 fraction from a naphtha feed for propylene generation
EP2147083A1 (fr) 2007-04-13 2010-01-27 Shell Internationale Research Maatschappij B.V. Systèmes et procédés de fabrication d'un produit distillé intermédiaire et d'oléfines inférieures à partir d'une charge d'hydrocarbure
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CN101747129B (zh) * 2008-11-28 2013-09-04 中国石油化工股份有限公司 一种催化转化生产低碳烯烃的方法
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CN105582997B (zh) * 2014-10-21 2018-05-18 中国石油化工股份有限公司 石脑油催化裂解产丙烯的催化剂及其制备方法和石脑油催化裂解产丙烯的方法
CN113046114B (zh) 2015-12-22 2024-04-16 沙特基础工业全球技术公司 由石脑油生产乙烯和丙烯的方法
US12064752B2 (en) * 2019-03-18 2024-08-20 ExxonMobil Technology and Engineering Company Mesoporous catalyst compounds and uses thereof
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KR20220117899A (ko) * 2019-12-23 2022-08-24 셰브런 유.에스.에이.인크. 정제 fcc 장치를 통한 플라스틱 폐기물의 폴리프로필렌으로의 순환 경제
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US6093867A (en) * 1998-05-05 2000-07-25 Exxon Research And Engineering Company Process for selectively producing C3 olefins in a fluid catalytic cracking process
US6118035A (en) * 1998-05-05 2000-09-12 Exxon Research And Engineering Co. Process for selectively producing light olefins in a fluid catalytic cracking process from a naphtha/steam feed
US6106697A (en) * 1998-05-05 2000-08-22 Exxon Research And Engineering Company Two stage fluid catalytic cracking process for selectively producing b. C.su2 to C4 olefins

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2012088852A1 (fr) 2010-12-28 2012-07-05 中国科学院大连化学物理研究所 Procédé pour le craquage catalytique d'un naphta couplé à du méthanol utilisant un catalyseur à tamis moléculaire zsm-5 modifié
US9284235B2 (en) 2010-12-28 2016-03-15 Dalian Institute Of Chemical Physics, Chinese Academy Of Sciences Process for methanol coupled catalytic cracking reaction of naphtha using a modified ZSM-5 molecular sieve catalyst

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JP2004516334A (ja) 2004-06-03
EP1261649A2 (fr) 2002-12-04
AU2001243379A1 (en) 2001-09-12
EP1261648A2 (fr) 2002-12-04
CA2400382A1 (fr) 2001-09-07
MXPA02008554A (es) 2003-04-22
WO2001064763A3 (fr) 2002-01-31
MXPA02008553A (es) 2003-03-12
CA2400524A1 (fr) 2001-09-07
WO2001064761A3 (fr) 2002-01-03
WO2001064762A3 (fr) 2002-01-24
WO2001064760A2 (fr) 2001-09-07
WO2001064760A3 (fr) 2002-01-03
CN1406252A (zh) 2003-03-26
CA2400598A1 (fr) 2001-09-07
CN1406253A (zh) 2003-03-26
AU2001241916A1 (en) 2001-09-12
EP1259555A2 (fr) 2002-11-27
AU2001239991A1 (en) 2001-09-12
JP2003525323A (ja) 2003-08-26
WO2001064763A2 (fr) 2001-09-07
MXPA02008552A (es) 2003-03-12
CN1406254A (zh) 2003-03-26
AU2001239990A1 (en) 2001-09-12
JP2004516335A (ja) 2004-06-03

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