GB732537A - Improvements in or relating to hydrocarbon conversion - Google Patents

Improvements in or relating to hydrocarbon conversion

Info

Publication number
GB732537A
GB732537A GB27414/51A GB2741451A GB732537A GB 732537 A GB732537 A GB 732537A GB 27414/51 A GB27414/51 A GB 27414/51A GB 2741451 A GB2741451 A GB 2741451A GB 732537 A GB732537 A GB 732537A
Authority
GB
United Kingdom
Prior art keywords
catalyst
line
regeneration
zone
filters
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.)
Expired
Application number
GB27414/51A
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.)
MW Kellogg Co
Original Assignee
MW Kellogg Co
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
Application filed by MW Kellogg Co filed Critical MW Kellogg Co
Publication of GB732537A publication Critical patent/GB732537A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING 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
    • C10G11/00Catalytic cracking, in the absence of hydrogen, of hydrocarbon oils
    • C10G11/14Catalytic cracking, in the absence of hydrogen, of hydrocarbon oils with preheated moving solid catalysts
    • C10G11/18Catalytic cracking, in the absence of hydrogen, of hydrocarbon oils with preheated moving solid catalysts according to the "fluidised-bed" technique
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING 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
    • C10G35/00Reforming naphtha
    • C10G35/04Catalytic reforming
    • C10G35/10Catalytic reforming with moving catalysts
    • C10G35/14Catalytic reforming with moving catalysts according to the "fluidised-bed" technique

Landscapes

  • 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)
  • Catalysts (AREA)
  • Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
  • Exhaust Gas Treatment By Means Of Catalyst (AREA)

Abstract

Hydroforming of naphtha is carried out in the presence of a fluidized bed of MoO3 and SiO2 on alumina gel catalyst at a temperature of about 950 DEG F. and a pressure of about 500 p.s.i.g.; catalyst is circulated through a regeneration zone in which the velocity of regeneration gas is increased from below 5 feet per second to above 10 feet per second in order to carry an entrained stream of catalyst to an upper collection zone (see Group III). Circulation of the catalyst is effected by pressure differences and fluistatic pressure in the transfer lines.ALSO:Catalyst which has been used as a dense fluidized bed in reactor 18 for the conversion of hydrocarbons is transferred in the dense phase via line 32 to combustion zone 30A where, in order to remove deactivating deposits, <PICT:0732537/III/1> it is treated in the dense phase with regeneration gas introduced at 58 and having a superficial velocity of below about 5 feet per sec.; the gas velocity increases to above about 10 feet per sec. in zone 30B, so that the regenerated catalyst is entrained and carried to collection zone 30C, where the gas velocity is reduced and catalyst separates as a dense phase and is returned via line 64 to the reactor. Circulation of the catalyst is effected by pressure differences and fluistatic pressure in the transfer lines. Catalyst is removed from the reactor at various points through lines 34, 36, 38, 40; safety valve 50 is automatically closed when the pressure difference across valves 50, 52 falls, and valve 52 is regulated according to the carbon content of the catalyst in line 32. The flue gas from collection zone 30C passes through porous filters 56 to cooler 84; part is discharged through line 74, and the remainder flows through line 88 to compressor 94, being divided into two streams, one passing through line 108 and heater 110 for blowing back the filters 56, and the other passing through line 106 to mix with regeneration air; auxiliary filter 96 is brought into use if there is a breakdown of the filters 56. Regeneration temperature is controlled (e.g. at 750-1150 DEG F.) by varying the relative proportions of air and recycled flue gas. Catalyst return line 64 includes safety valve 66, operating similarly to valve 50, and valve 68 which is regulated according to the bed level 60 in the collection zone. Controller 70 operates flue gas outlet valve 72 in order to maintain a desired pressure differential between the reactor and regenerator. Time controller 78 regulates the blowing back of filters 56 in sequence. In Fig. 2 (not shown), acceleration of the flue gas takes place in a series of parallel tubes surrounded by a cooler, and part of the regenerated catalyst is recirculated from the collector to the bottom of the regeneration zone. The amount of catalyst recirculated provides an additional control of the regeneration temperature. In Fig. 3 (not shown), the flue gas is not recirculated, heated air being used for blowing back the filters. The process is described with reference to the hydroforming of naphthas (see Group IV (b)), using a catalyst consisting of MoO3 and SiO2 on alumina gel, but is also applicable in hydrodesulphurization, hydrogenation, and hydrocracking.
GB27414/51A 1950-11-30 1951-11-22 Improvements in or relating to hydrocarbon conversion Expired GB732537A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US732512XA 1950-11-30 1950-11-30

Publications (1)

Publication Number Publication Date
GB732537A true GB732537A (en) 1955-06-29

Family

ID=22112643

Family Applications (2)

Application Number Title Priority Date Filing Date
GB27414/51A Expired GB732537A (en) 1950-11-30 1951-11-22 Improvements in or relating to hydrocarbon conversion
GB19346/53A Expired GB732512A (en) 1950-11-30 1951-11-22 Improvements in refining the products of a catalytic hydrocarbon conversion process

Family Applications After (1)

Application Number Title Priority Date Filing Date
GB19346/53A Expired GB732512A (en) 1950-11-30 1951-11-22 Improvements in refining the products of a catalytic hydrocarbon conversion process

Country Status (2)

Country Link
FR (1) FR1048964A (en)
GB (2) GB732537A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105733647B (en) * 2014-12-09 2018-05-01 中科合成油工程股份有限公司 The method that liquefied petroleum gas is recycled from Fischer-Tropsch process exhaust

Also Published As

Publication number Publication date
FR1048964A (en) 1953-12-28
GB732512A (en) 1955-06-22

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