GB900374A - Combined steam cracker and butene dehydrogenation light ends - Google Patents

Combined steam cracker and butene dehydrogenation light ends

Info

Publication number
GB900374A
GB900374A GB36728/60A GB3672860A GB900374A GB 900374 A GB900374 A GB 900374A GB 36728/60 A GB36728/60 A GB 36728/60A GB 3672860 A GB3672860 A GB 3672860A GB 900374 A GB900374 A GB 900374A
Authority
GB
United Kingdom
Prior art keywords
tower
overhead
steam
light ends
line
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
GB36728/60A
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 Technology and Engineering Co
Original Assignee
Exxon Research and Engineering Co
Esso Research and Engineering 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 Exxon Research and Engineering Co, Esso Research and Engineering Co filed Critical Exxon Research and Engineering Co
Publication of GB900374A publication Critical patent/GB900374A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C7/00Purification; Separation; Use of additives
    • C07C7/005Processes comprising at least two steps in series

Abstract

<FORM:0900374/IV (b)/1> Hydrocarbons are separately recovered from the light ends from a steam cracker operated to produce olefins and diolefins and a butene dehydrogenation unit employing two or more reactors, one or more of which is in stream while one is being regenerated, by combining the two streams, compressing to above 150 p.s.i.g. and passing to an absorption/fractionation system to recover the separate components. A naphtha or gas oil, e.g. boiling in the range 350-700 DEG F. is supplied with steam to furnace 2 operated at 1300-1500 DEG F., 0-50 p.s.i.g. with residence times of 0.05-1 second. The effluent is quenched to 400-600 DEG F. with heavy oil supplied through line 4 and passed to distillation tower 6 where tar, quench oil, and gas oil are separated from light ends recovered overhead. These are cooled to 75-125 DEG F. and C6- materials passed to compressor 14 and heavier materials removed through line 15. A butane/butene feed containing 70-95% mol butenes is heated in furnace 18 and contacted with catalyst in one of reactors 22 and 29, the other being on regeneration. Using calcium nickel phosphate as catalyst the feed is mixed with steam and passed at 1,000-1,400 DEG F. into the reactor with a butene gas rate of 75-200 v/v/hr. and a steam rate of 1,400-4,000 v/v/hr. and a pressure of 15-30 p.s.i.a. Using chromia alumina the temperature may be 1,000-1,200 DEG F. at 1-15 p.s.i.a. with a WHSV of 0.5-1.5 wt./hr./wt. On switching reactors from on stream to regeneration the effluent rate fluctuates, the fluctuation being diminished by combining with the steam cracker light ends before passing to the compressor 14. Steam if present is condensed out in separator 33. The combined stream cooled to 75-125 DEG F. and in separator 39 C3- are taken overhead through line 40 while heavier materials pass with material in line 15 to naphtha splitter 42 where C6+ materials are removed as bottoms while the overhead is caustic treated to remove sulphur compounds and CO2 and passed to absorber de-ethaniser 47.C3- compounds in line 40 are treated with diethanolamine for removal of H2S and CO2 in tower 48 and with a caustic wash in tower 53 before passing to absorber de-ethaniser 47. Here the vapours are treated with a C5 lean oil obtaining a C2- stream overhead. This is washed with sponge oil in tower 59 to remove traces of C5 lean oil. C2-product is recovered in line 60. The C3+ material from the bottom of tower 47 is fractionated in tower 62 to obtain C5 products as bottoms, part being used as the C5 lean oil in tower 47. The overhead is split in tower 69 into C3 overhead and C4 bottoms which latter passes to butadiene extraction. Generally in the combined light ends the C4/C3 ratio will be 0.7-2:1 and the butene dehydrogenation effluent will be 5-50% by volume of the steam cracker light ends. The debutaniser 62 can be operated at less than 140 p.s.i.g., i.e. lower than a conventional steam cracker debutaniser.
GB36728/60A 1959-11-02 1960-10-26 Combined steam cracker and butene dehydrogenation light ends Expired GB900374A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US850250A US3154482A (en) 1959-11-02 1959-11-02 Combined steam cracker and butene dehydrogenation light ends

Publications (1)

Publication Number Publication Date
GB900374A true GB900374A (en) 1962-07-04

Family

ID=25307644

Family Applications (1)

Application Number Title Priority Date Filing Date
GB36728/60A Expired GB900374A (en) 1959-11-02 1960-10-26 Combined steam cracker and butene dehydrogenation light ends

Country Status (3)

Country Link
US (1) US3154482A (en)
DE (1) DE1418782A1 (en)
GB (1) GB900374A (en)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3390075A (en) * 1966-05-02 1968-06-25 Phillips Petroleum Co Process for recovering hydrocarbon gases from streams thereof containing h2s
US3425931A (en) * 1966-12-05 1969-02-04 Universal Oil Prod Co Hydrocarbon recovery method
US3477946A (en) * 1967-12-28 1969-11-11 Universal Oil Prod Co Absorption process
US5444176A (en) * 1992-10-28 1995-08-22 Exxon Chemical Patents Inc. Process for recovering olefins from cat-cracked gas without accumulating undesirable oxides of nitrogen
US7749372B2 (en) * 2005-07-08 2010-07-06 Exxonmobil Chemical Patents Inc. Method for processing hydrocarbon pyrolysis effluent

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2181302A (en) * 1937-04-29 1939-11-28 Polymerization Process Corp Conversion of hydrocarbons
US2382473A (en) * 1941-03-13 1945-08-14 Phillips Petroleum Co Production of butadiene
US2391555A (en) * 1941-06-16 1945-12-25 Shell Dev Production of dienes
US2429980A (en) * 1942-11-27 1947-11-04 Lion Oil Co Process of conducting chemical reactions
US2458082A (en) * 1946-08-06 1949-01-04 Phillips Petroleum Co Production of diolefins
US2745889A (en) * 1953-06-22 1956-05-15 Exxon Research Engineering Co Separation of c2, c3 and c4 alkenes from highly cracked distillates
US2831041A (en) * 1954-09-30 1958-04-15 California Research Corp Dehydrogenation process
US2750435A (en) * 1954-12-17 1956-06-12 Phillips Petroleum Co Process for separation of c4 hydrocarbons and solvent therefor
US2945804A (en) * 1957-03-11 1960-07-19 Exxon Research Engineering Co Hydroformate feed improved by adsorption of normal paraffins
US2943041A (en) * 1958-06-09 1960-06-28 Exxon Research Engineering Co Processing of steam-cracked naphtha light end products
US2972646A (en) * 1958-07-29 1961-02-21 Exxon Research Engineering Co Separation of butadiene

Also Published As

Publication number Publication date
DE1418782A1 (en) 1968-10-24
US3154482A (en) 1964-10-27

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