EP0842242A4 - Procede d'hydrodesulfuration - Google Patents

Procede d'hydrodesulfuration

Info

Publication number
EP0842242A4
EP0842242A4 EP96923485A EP96923485A EP0842242A4 EP 0842242 A4 EP0842242 A4 EP 0842242A4 EP 96923485 A EP96923485 A EP 96923485A EP 96923485 A EP96923485 A EP 96923485A EP 0842242 A4 EP0842242 A4 EP 0842242A4
Authority
EP
European Patent Office
Prior art keywords
range
column reactor
εaid
petroleum
distillation column
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.)
Granted
Application number
EP96923485A
Other languages
German (de)
English (en)
Other versions
EP0842242A1 (fr
EP0842242B1 (fr
Inventor
Dennis Hearn
Hugh M Putman
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.)
Chemical Research and Licensing Co
Original Assignee
Chemical Research and Licensing 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 Chemical Research and Licensing Co filed Critical Chemical Research and Licensing Co
Publication of EP0842242A1 publication Critical patent/EP0842242A1/fr
Publication of EP0842242A4 publication Critical patent/EP0842242A4/fr
Application granted granted Critical
Publication of EP0842242B1 publication Critical patent/EP0842242B1/fr
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

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
    • C10G45/00—Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds
    • C10G45/02—Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds to eliminate hetero atoms without changing the skeleton of the hydrocarbon involved and without cracking into lower boiling hydrocarbons; Hydrofinishing

Definitions

  • the present invention relates to the hydrodesulfurization of petroleum streams in a distillation column reactor. More particularly the invention relates to a process wherein a petroleum fraction is fed to a distillation column reactor containing a hydrodesulfurization catalyst in the form of a catalytic distillation structure where the organic sulfur compounds contained in the petroleum fraction are reacted with hydrogen to form H2S which can be stripped from the overhead product.
  • Petroleum distillate streams contain a variety of organic chemical components. Generally the streams are defined by their boiling ranges which determine the compositions. The processing of the streams also affects the composition.
  • products from either catalytic cracking or thermal cracking processes contain high concentrations of olefinic materials as well as saturated (alkanes) materials and polyunsaturated materials (diolefins) . Additionally, these components may be any of the various isomers of the compounds.
  • Organic sulfur compounds present in these petroleum fractions are denoted as, "sulfur".
  • the amount of sulfur is generally dependent upon the crude source. For instance the Saudi Arabian crudes are generally high in sulfur as are certain domestic crudes. Kuwaiti, Cambodian and Louisiana crudes are generally low in sulfur.
  • the type of sulfur compounds will also depend on the boiling range of a given stream. Generally the lower boiling fractions contain mercaptans while the heavier boiling fractions contain thiophenic and heterocyclic sulfur compounds.
  • the organic sulfur compounds are almost always considered to be contaminants. They hinder in downstream processing and at the very least make obnoxious SO2 gas when burned. For these reasons it is very desirable to remove these compounds. The degree of removal is dependent upon the use of the fraction. For instance, feed streams to catalytic reforming require extremely low sulfur con ⁇ centrations (less than 1 wppm) .
  • Current EPA regulations call for combustible motor fuels such as gasoline, kerosene or diesel to have no more than about 500 wppm sulfur. It is expected that in the future the sulfur specification will be lowered to about 50 wppm, especially for gasoline.
  • HDS hydrodesulfurization
  • the product is fractionated or simply flashed to release the hydrogen sulfide and collect the now sweetened fraction.
  • Patent 4,443,559, 5,057,468, 5262,012 5,266,546 and 5,348,710 disclose a variety of catalyst structures for this use and are incorporated by reference herein.
  • a distillation column reactor has been utilized wherein a solid particulate catalyst has been placed within a distillation column so as to act as a distillation structure.
  • the distillation column reactor has been found to be particularly useful in equilibrium limited reactions because the reaction products have been removed from the reaction zone almost immediately. Additionally the distillation column reactor has been found to be useful to prevent unwanted side reactions.
  • the present invention uses catalytic distillation in hydrodesulfurization at low total pressures below about 300 psig, preferably below about 290 and more preferably in the range of 0 to 200 psig, low hydrogen partial pressure in the range of 0.1 to 70 psi and temperatures in the range of 400 to 800 °F.
  • the invention may be said to comprise: feeding (1) a petroleum stream containing sulfur compounds and (2) hydrogen to a distillation column reactor; concurrently in said distillation column reactor
  • the mechanism that produces the effectiveness of the present process is the condensation of a portion of the vapors in the reaction system, which occludes sufficient hydrogen in the condensed liquid to obtain the requisite intimate contact between the hydrogen and the sulfur compounds in the presence of the catalyst to result in their hydrogenation.
  • the result of the operation of the process in the catalytic distillation mode is that lower hydrogen partial pressures (and thus lower total pressures) may be used.
  • any distillation there is a temperature gradient within the distillation column reactor.
  • the temperature at the lower end of the column contains higher boiling material and thus is at a higher temperature than the upper end of the column.
  • the lower boiling fraction which contains more easily removable sulfur compounds, is subjected to lower temperatures at the top of the column which provides for greater selectivity, that is, less hydrocracking or saturation of desirable olefinic compounds.
  • the higher boiling portion is subjected to higher temperatures in the lower end of the distillation column reactor to crack open the sulfur containing ring compounds and hydrogenate the sulfur. It is believed that in the present reaction catalytic distillation is a benefit first, because the reaction is occurring concurrently with distillation, the initial reaction products and other stream components are removed from the reaction zone as quickly as possible reducing the likelihood of side reactions.
  • Petroleum fractions which may be treated to remove sulfur by the instant process include the full range of petroleum distillates and include natural gas liquids, naphthas, kerosene, diesel, gas oils (both atmospheric and vacuum) and residuums.
  • the fractions may be straight run material direct from a crude fractionation unit or may be the result of downstream processing, such as fluid catalytic cracking, pyrolysis or delayed coking.
  • the hydrogen rate to the reactor must be sufficient to maintain the reaction, but kept below that which would cause flooding of the column which is understood to be the "effectuating amount of hydrogen " as that term is used herein.
  • the mole ratio of hydrogen to sulfur compound in the feed varies according to the type of compound and the amount of hydrogen expected to be consumed by side reac- tions such as double or triple bond saturation.
  • Hydrogen flow rates are typically calculated as standard cubic feet per barrel of feed (SCFB) and are in the range of 300 to 3000 SCFB.
  • a low total pressure below about 300 psig, for example in the range of 0 to 200 psig is required for the hydrodesulfurization and hydrogen partial pressure of less than 70 psi down to 0.1 psig can be employed, e.g. 0.1 to 70 psig preferably about 0.5 to 10 psig.
  • the preferred hydrogen partial pressure is less than 50 psig. This preferably is a hydrogen partial pressure in the range of about 0.1 to 10 psia and even more preferably no more than 7 psia. Optimal results have been obtained in the range between 0.5 and 50 psig hydrogen partial pressure.
  • typical conditions are overhead temperature in the range of 350 to 550 °F, the bottoms temperature in the range of 500 to 800 °F, and the pressure in the range of 25 to less than 300 psig.
  • typical conditions are overhead temperature in the range of 350 to 650 °F, the bottoms temperature in the range of 500 to 800 ⁇ F, and the pressure in the range of 0 to 200 psig.
  • typical conditions are overhead temperature in the range of 350 to 650 °F, the bottoms temperature in the range 500 to 850 °F, and the pressure in the range 0 to 150 psig.
  • Catalyst which are useful for the hydrodesulfurization reaction include metals Group VIII such as cobalt, nickel, palladium, alone or in combination with other metals such as molybdenum or tungsten on a suitable support which may be alumina, silica-alumina, titania-zirconia or the like. Normally the metals are provided as the oxides of the metals supported on extrudates or spheres and as such are not generally useful as distillation structures.
  • the catalysts contain components from Group V, VIB, VIII metals of the Periodic Table or mixtures thereof.
  • the use of the distillation system reduces the deactivation and provides for longer runs than the fixed bed hydrogenation units of the prior art.
  • the Group VIII metal provides increased overall average activity.
  • Catalysts containing a Group VIB metal such as molybdenum and a Group VIII such as cobalt or nickel are preferred.
  • Catalysts suitable for the hyrodesulfurization reaction include cobalt-molybdenum, nickel-molybdenum and nickel-tungsten.
  • the metals are generally present as oxides supported on a neutral base such as alumina, silica-alumina or the like. The metals are reduced to the sulfide either in use or prior to use by exposure to sulfur compound containing streams.
  • Table I The properties of a typical hydrodesulfurization catalyst in Table I below.
  • the catalytic material is a component of a distillation system functioning as both a catalyst and distillation packing, i.e., a packing for a distillation column having both a distillation function and a catalytic function.
  • a preferred catalyst structure for the present hydrogenation reaction comprises flexible, semi-rigid open mesh tubular material, such as stainless steel wire mesh, filled with a particulate catalytic material in one of several embodiments recently developed in conjunction with the present process.
  • the new catalyst structure is a catalytic distillation structure comprising flexible, semi-rigid open mesh tubular material, such as stainless steel wire mesh, filled with a particulate catalytic material said tubular material having two ends and having a length in the range of from about one-half to twice the diameter of ⁇ aid tubular material, a first end being sealed together along a fir ⁇ t axis to form a first seam and a second end being sealed together along a second axis to form a second seam wherein the plane of the first seam along the axis of said tubular material and the plane of the second seam along the axis of said tubular material bisect each other at an angle of about 15 to 90°.
  • a catalytic distillation structure comprising flexible, semi-rigid open mesh tubular material, such as stainless steel wire mesh, filled with a particulate catalytic material said tubular material having two ends and having a length in the range of from about one-half to twice the diameter of ⁇ aid tubular material, a first end
  • US Patent No. 4,242,530 and US Pat. No. 4,443,559 which are incorporated herein, disclo ⁇ e supported catalyst in a plurality of pockets in a cloth belt or wire mesh tubular structures, which is supported in the distillation column reactor by open mesh knitted stainless steel wire by twisting the two together into a helix.
  • U.S. Pat. No. 5,348,710 which is incorporated herein, describes several other suitable structures in the prior art and discloses new structures suitable for this process.
  • Other catalytic distillation structures useful for this purpose are disclosed in U.S. patents 4,731,229 and 5,073,236 which are also incorporated by reference.
  • the particulate catalyst material may be a powder, small irregular chunks or fragments, small beads and the like.
  • the particular form of the catalytic material in the structure is not critical, so long as sufficient surface area is provided to allow a reasonable reaction rate.
  • the sizing of catalyst particles can be best determined for each catalytic material (since the porosity or available internal surface area will vary for different material and of course affect the activity of the catalytic material) .
  • the preferred catalyst structures for the packing are those employing the more open ⁇ tructure of permeable plates or screen wire.
  • Example 1 A full boiling range naphtha was fed to the distillation column reactor containing a the catalyst prepared as noted above. Conditions and results are given in TABLE II below. TABLE II
  • Feed rate lbs/hr 1.00 total sulfur, wppm (mg) 1528 (694)
  • Example 3 A die ⁇ el fraction wa ⁇ fed to the di ⁇ tillation column reactor as described above. Conditions and results are given in TABLE IV below. TABLE IV

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)
  • Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)

Abstract

L'invention concerne un procédé d'hydrodésulfuration de flux de pétrole consistant à mettre en contact le flux de pétrole contenant du soufre avec de l'hydrogène, à une pression partielle inférieure à 70 psig, dans un réacteur de colonne de distillation contenant un catalyseur d'hydrodésulfuration sous forme d'une structure de distillation catalytique.
EP96923485A 1995-07-10 1996-06-27 Procede d'hydrodesulfuration Expired - Lifetime EP0842242B1 (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US50010095A 1995-07-10 1995-07-10
US500100 1995-07-10
PCT/US1996/010971 WO1997003149A1 (fr) 1995-07-10 1996-06-27 Procede d'hydrodesulfuration

Publications (3)

Publication Number Publication Date
EP0842242A1 EP0842242A1 (fr) 1998-05-20
EP0842242A4 true EP0842242A4 (fr) 1999-04-14
EP0842242B1 EP0842242B1 (fr) 2004-04-07

Family

ID=23988030

Family Applications (1)

Application Number Title Priority Date Filing Date
EP96923485A Expired - Lifetime EP0842242B1 (fr) 1995-07-10 1996-06-27 Procede d'hydrodesulfuration

Country Status (11)

Country Link
EP (1) EP0842242B1 (fr)
JP (1) JP3819030B2 (fr)
KR (1) KR100437965B1 (fr)
CN (1) CN1074038C (fr)
AU (1) AU6398496A (fr)
CA (1) CA2226632C (fr)
DE (1) DE69632135T2 (fr)
ES (1) ES2214544T3 (fr)
MX (1) MX9800298A (fr)
RU (1) RU2157399C2 (fr)
WO (1) WO1997003149A1 (fr)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5961815A (en) * 1995-08-28 1999-10-05 Catalytic Distillation Technologies Hydroconversion process
US5894076A (en) * 1997-05-12 1999-04-13 Catalytic Distillation Technologies Process for alkylation of benzene
US6103773A (en) * 1998-01-27 2000-08-15 Exxon Research And Engineering Co Gas conversion using hydrogen produced from syngas for removing sulfur from gas well hydrocarbon liquids
CN1076753C (zh) * 1998-06-25 2001-12-26 中国石油化工集团公司 一种石油馏分临氢/加氢精制工艺
US6413413B1 (en) * 1998-12-31 2002-07-02 Catalytic Distillation Technologies Hydrogenation process
DE19953486C2 (de) * 1999-11-06 2003-08-14 Siemens Ag Verfahren zur Synchronisation einer Signalübertragung in Aufwärtsrichtung in einem Funk-Kommunikationssystem
US6676830B1 (en) * 2001-09-17 2004-01-13 Catalytic Distillation Technologies Process for the desulfurization of a light FCC naphtha
US7153415B2 (en) * 2002-02-13 2006-12-26 Catalytic Distillation Technologies Process for the treatment of light naphtha hydrocarbon streams
GB0226178D0 (en) 2002-11-11 2002-12-18 Johnson Matthey Plc Desulphurisation
FR2997415B1 (fr) * 2012-10-29 2015-10-02 IFP Energies Nouvelles Procede de production d'une essence a basse teneur en soufre

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4194964A (en) * 1978-07-10 1980-03-25 Mobil Oil Corporation Catalytic conversion of hydrocarbons in reactor fractionator
US4232177A (en) * 1979-02-21 1980-11-04 Chemical Research & Licensing Company Catalytic distillation process
US4213847A (en) * 1979-05-16 1980-07-22 Mobil Oil Corporation Catalytic dewaxing of lubes in reactor fractionator
US5173173A (en) * 1990-09-28 1992-12-22 Union Oil Company Of California Trace contaminant removal in distillation units

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
No further relevant documents disclosed *
See also references of WO9703149A1 *

Also Published As

Publication number Publication date
AU6398496A (en) 1997-02-10
CN1189183A (zh) 1998-07-29
DE69632135T2 (de) 2005-03-03
KR100437965B1 (ko) 2004-09-13
CN1074038C (zh) 2001-10-31
CA2226632C (fr) 2007-05-29
ES2214544T3 (es) 2004-09-16
WO1997003149A1 (fr) 1997-01-30
MX9800298A (es) 1998-07-31
CA2226632A1 (fr) 1997-01-30
JP2000505118A (ja) 2000-04-25
DE69632135D1 (de) 2004-05-13
EP0842242A1 (fr) 1998-05-20
RU2157399C2 (ru) 2000-10-10
KR19990028564A (ko) 1999-04-15
JP3819030B2 (ja) 2006-09-06
EP0842242B1 (fr) 2004-04-07

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