US20040149629A1 - Process for the preparation of and composition of a feedstock usable for the preparation of lower olefins - Google Patents
Process for the preparation of and composition of a feedstock usable for the preparation of lower olefins Download PDFInfo
- Publication number
- US20040149629A1 US20040149629A1 US10/358,129 US35812903A US2004149629A1 US 20040149629 A1 US20040149629 A1 US 20040149629A1 US 35812903 A US35812903 A US 35812903A US 2004149629 A1 US2004149629 A1 US 2004149629A1
- Authority
- US
- United States
- Prior art keywords
- fraction
- hydrocarbon feed
- boiling point
- synthetic
- naphtha
- 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.)
- Abandoned
Links
- 238000000034 method Methods 0.000 title claims abstract description 77
- 150000001336 alkenes Chemical class 0.000 title claims abstract description 70
- 238000002360 preparation method Methods 0.000 title claims abstract description 22
- 239000000203 mixture Substances 0.000 title claims abstract description 16
- 229930195733 hydrocarbon Natural products 0.000 claims abstract description 84
- 150000002430 hydrocarbons Chemical class 0.000 claims abstract description 84
- 239000004215 Carbon black (E152) Substances 0.000 claims abstract description 71
- 238000004227 thermal cracking Methods 0.000 claims abstract description 27
- 239000000047 product Substances 0.000 claims description 62
- 238000009835 boiling Methods 0.000 claims description 45
- 238000006243 chemical reaction Methods 0.000 claims description 28
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims description 18
- 238000005336 cracking Methods 0.000 claims description 17
- 230000015572 biosynthetic process Effects 0.000 claims description 11
- 238000003786 synthesis reaction Methods 0.000 claims description 11
- 239000007788 liquid Substances 0.000 claims description 10
- 238000002156 mixing Methods 0.000 claims description 10
- 238000004519 manufacturing process Methods 0.000 claims description 9
- 238000004517 catalytic hydrocracking Methods 0.000 claims description 8
- 239000003345 natural gas Substances 0.000 claims description 4
- 239000007795 chemical reaction product Substances 0.000 claims description 3
- 239000003208 petroleum Substances 0.000 claims description 2
- 239000001993 wax Substances 0.000 description 11
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 8
- 239000000463 material Substances 0.000 description 7
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 7
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 7
- 239000005977 Ethylene Substances 0.000 description 6
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 6
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 5
- 239000003054 catalyst Substances 0.000 description 5
- -1 ethylene, propylene Chemical group 0.000 description 5
- 239000007789 gas Substances 0.000 description 5
- 239000001257 hydrogen Substances 0.000 description 5
- 229910052739 hydrogen Inorganic materials 0.000 description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- 238000004821 distillation Methods 0.000 description 4
- 238000005984 hydrogenation reaction Methods 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 239000010454 slate Substances 0.000 description 4
- 229910017052 cobalt Inorganic materials 0.000 description 3
- 239000010941 cobalt Substances 0.000 description 3
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 3
- 239000012263 liquid product Substances 0.000 description 3
- 150000002739 metals Chemical class 0.000 description 3
- 229910052759 nickel Inorganic materials 0.000 description 3
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 2
- 150000001345 alkine derivatives Chemical class 0.000 description 2
- 229910002091 carbon monoxide Inorganic materials 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 239000010687 lubricating oil Substances 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 229910052707 ruthenium Inorganic materials 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 238000004230 steam cracking Methods 0.000 description 2
- 239000002028 Biomass Substances 0.000 description 1
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
- 239000005864 Sulphur Substances 0.000 description 1
- 229910021536 Zeolite Inorganic materials 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 239000011959 amorphous silica alumina Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000010953 base metal Substances 0.000 description 1
- 230000001588 bifunctional effect Effects 0.000 description 1
- 230000008033 biological extinction Effects 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000003245 coal Substances 0.000 description 1
- 239000000571 coke Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 239000010779 crude oil Substances 0.000 description 1
- 238000006356 dehydrogenation reaction Methods 0.000 description 1
- 150000001993 dienes Chemical class 0.000 description 1
- 239000002283 diesel fuel Substances 0.000 description 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
- 238000005194 fractionation Methods 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 239000000295 fuel oil Substances 0.000 description 1
- ZZUFCTLCJUWOSV-UHFFFAOYSA-N furosemide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC(C(O)=O)=C1NCC1=CC=CO1 ZZUFCTLCJUWOSV-UHFFFAOYSA-N 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 229910000510 noble metal Inorganic materials 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 238000005504 petroleum refining Methods 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000002352 steam pyrolysis Methods 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- 238000010626 work up procedure Methods 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
Images
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
- C10G9/00—Thermal non-catalytic cracking, in the absence of hydrogen, of hydrocarbon oils
-
- 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
- C10G69/00—Treatment of hydrocarbon oils by at least one hydrotreatment process and at least one other conversion process
- C10G69/02—Treatment of hydrocarbon oils by at least one hydrotreatment process and at least one other conversion process plural serial stages only
- C10G69/06—Treatment of hydrocarbon oils by at least one hydrotreatment process and at least one other conversion process plural serial stages only including at least one step of thermal cracking in the absence of hydrogen
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/04—Liquid carbonaceous fuels essentially based on blends of hydrocarbons
-
- 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
- C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
- C10G2300/10—Feedstock materials
- C10G2300/1022—Fischer-Tropsch products
-
- 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
- C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
- C10G2300/20—Characteristics of the feedstock or the products
- C10G2300/30—Physical properties of feedstocks or products
- C10G2300/301—Boiling range
-
- 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 invention relates to a process for the preparation of lower olefins and a composition of a high performance feedstock usable in a process for the preparation of lower olefins from a hydrocarbon containing feed including at least a fraction boiling above the boiling point range of the lower olefins.
- this feedstock can be used advantageously when the lower olefins process objective is propylene.
- the thermal cracking process for production of lower olefins is the most important commercial route for the production of ethylene, propylene and other lower olefins from a hydrocarbon containing feed including at least a fraction above the boiling point range of the lower olefins.
- the thermal cracking of naphtha feedstocks proceeds in two stages.
- the primary reactions that take place in the first stage include the thermal decomposition of the reactants by free-radical chain mechanism into hydrogen, methane, ethylene, propylene, butylenes and higher olefins.
- the second stage involves three types of reactions:
- FT Fischer-Tropsch
- FT reactors FT products
- the FT process is a well known process in which carbon monoxide and hydrogen are reacted over an iron, cobalt, nickel or ruthenium containing catalyst to produce a mixture of straight and branched chain hydrocarbons ranging from methane to waxes and smaller amounts of oxygenates.
- the FT process is used industrially to convert synthesis gas, which might derived from coal, natural gas, biomass or heavy oil streams, into hydrocarbons ranging from methane to species with molecular masses above 1400.
- the main products are linear paraffinic materials
- other species such as branched paraffins, olefins and oxygenated components may form part of the product slate.
- the exact product slate depends on reactor configuration, operating conditions and the catalyst that is employed, as is evident from articles such as Catal.Rev.-Sci. Eng., 23(1&2), 265-278 (1981).
- Preferred reactors for the production of heavier hydrocarbons are slurry bed or tubular fixed bed reactors, while operating conditions are preferably in the range of 160-280° C., in some cases in the 210-260° C. range, and 18-50 bar, in some cases preferably between 20-30 bar.
- the catalyst may comprise active metals such as iron, cobalt, nickel or ruthenium. While each catalyst will give its own unique product slate, in all cases the product slate contains some waxy, highly paraffinic material which needs to be further upgraded into usable products.
- the FT products can be hydroconverted into a range of final products, such as middle distillates, naphtha, solvents, lube oil bases, etc. Such hydroconversion, which usually consists of a range of processes such as hydrocracking, hydrotreatment and distillation, can be termed a FT products work-up process.
- the invention provides a process for the preparation of lower olefins from a synthetic hydrocarbon feed including at least a fraction having a boiling point above the boiling point range of the lower olefins, wherein the hydrocarbon feed includes an unhydrogenated fraction, which process includes the thermal processing of the hydrocarbon feed.
- the thermal processing may be thermal cracking of the synthetic hydrocarbon feed under thermal cracking conditions selected to suit the synthetic hydrocarbon feed composition.
- the thermal cracking conditions are a temperature of from 400° C. to 1200° C., usually from 700° C. to 950° C. and at a pressure of from 0.1 to 20 bar absolute pressure, typically from 1 to 5 bar.
- the residence time in a thermal cracking unit in which the thermal cracking is taking place may be from 50 ms to 1000 ms, or even longer. Typically the residence time may be below 300 ms. The residence time will however depend on the configuration of the thermal cracking unit used.
- the thermal cracking may be carried out in the presence of an inert media.
- This inert media might be steam or nitrogen.
- the synthetic hydrocarbon feed may be the product of a FT reaction.
- the synthetic hydrocarbon feed may be the processed product of the FT reaction.
- the unhydrogenated fraction of the synthetic hydrocarbon feed may be an unhydrogenated fraction of the process products of the FT reaction.
- the synthetic hydrocarbon feed may be prepared by combining at least
- an unhydrogenated fraction of the process products of the FT reaction also referred to as an unhydrogenated FT fraction
- a hydroconverted fraction of the process products of the FT reaction also referred to as a hydroprocessed or hydrocracked FT fraction.
- the unhydrogenated FT fraction may include a fraction of the condensate product of the FT reaction.
- the FT condensate is typically obtained as the liquid hydrocarbon stream from the FT products excluding the FT wax from a FT reactor in which the FT reaction has taken place.
- the hydroprocessed FT fraction may be a hydrocracked FT wax fraction of the FT reaction products.
- the FT wax fraction is typically obtained as the heavy hydrocarbons stream.
- the invention extends to a hydrocarbon feed to a cracking process for the preparation of lower olefins from a synthetic hydrocarbon feed including at least a fraction having a boiling point above the boiling point range of the lower olefins, said hydrocarbon feed including at least a fraction which is unhydrogenated.
- the synthetic hydrocarbon feed may be the product of a FT reaction.
- the synthetic hydrocarbon feed may be the processed product of the FT reaction.
- the synthetic hydrocarbon feed is optimised when the target product of the cracking process is propylene. Moreover, it has also been found that this synthetic hydrocarbon feed can yield significantly lower yields of the undesirable liquid product (C5+fraction) that is co-produced during cracking to lower olefins.
- This synthetic hydrocarbon feed also referred to as olefinic naphtha, also has a low aromatics content, typically below 1% mass, preferably below 0.5% mass. This is believed to be a contributing factor to the superior thermal cracking performance.
- the invention extends to a hydrocarbon feed to a cracking process for the preparation of lower olefins from a synthetic hydrocarbon feed including at least a fraction having a boiling point above the boiling point range of the lower olefins, said hydrocarbon feed comprising at least 15% olefins and at most 1.0% aromatics.
- the hydrocarbon feed may comprise at least about 20% olefins.
- a process for the preparation of a synthetic hydrocarbon feed to a process for producing lower olefins said feed including at least a fraction having a boiling point above the boiling point range of the lower olefins, said process including the steps of:
- step b) fractionating the hydroconverted wax product from step b) to obtain a hydroconverted naphtha fraction separated from the other products from the hydroconversion process;
- step d) blending said olefinic naphtha from step a) with the hydroconverted naphtha from step c) to obtain a synthetic hydrocarbon feed in a desired ratio having a boiling point above the boiling point range of the lower olefins.
- the wax fraction of step b) may have a true boiling point (TBP) in the range of about 70° C. to 700° C., typically in the range 80° C. to 650° C.
- TBP true boiling point
- the FT condensate fraction of step a) may have a true boiling point (TBP) in the range ⁇ 70° C. to 350° C., typically ⁇ 10° C. to 340° C., usually ⁇ 70° C. to 350° C.
- TBP true boiling point
- step c) is blended with the synthetic hydrocarbon fraction of step a) in a volumetric ratio of from 1:4 to 4:1 to form the synthetic hydrocarbon feed of step d).
- this volumetric ratio is 1:2 to 2:1, even more typically between 3:2 and 2:3.
- a process for the preparation of a synthetic hydrocarbon feed for a process for producing lower olefins said feed including at least a fraction having a boiling point above the boiling point range of the lower olefins, said process including the steps of:
- step b) blending said hydroconverted product from step a) with a straight run unhydrogenated condensate fraction in a desired ratio to obtain a blend that includes hydrocarbons boiling over a broad temperature range;
- step c) fractionating the hydrocarbons blend from step b) to obtain a synthetic hydrocarbon feed for the thermal cracking process having a boiling point above the boiling point range of the lower olefins.
- the hydroconverted product of step a) may be blended with the condensate hydrocarbon fraction in step b) in a volumetric ratio of from 1:10 to 10:1 before being fractionated in a single unit to form the synthetic hydrocarbon feed of step c).
- the wax fraction of step a) may have a true boiling point (TBP) in the range of about 70° C. to 700° C., typically in the range 80° C. to 650° C.
- the FT condensate fraction of step b) may have a true boiling point (TBP) in the range ⁇ 70° C. to 350° C., typically ⁇ 10° C. to 340° C., usually ⁇ 70° C. to 350° C.
- TBP true boiling point
- the synthetic hydrocarbon fraction usable as feedstock for thermal cracking may be a C5 to 160° C. boiling range, defined based on the ASTM D86 Distillation standard, synthetic naphtha.
- a semi-synthetic feedstock may be produced which is usable for the production of lower olefins via thermal cracking, said feedstock comprising an olefinic synthetic feedstock obtained from a FT synthesis product of H 2 and CO and a highly paraffinic fraction selected from a petroleum liquid fraction and a natural gas liquid fraction, blended to have at least a 15% mass olefins content and an aromatics content below 1%.
- the highly paraffinic naphtha may be a product obtained from conventional petroleum refining scheme or from the fractionation of the liquid hydrocarbons contained in natural gas.
- the blending ratio required is selected for each specific highly paraffinic naphtha in order to obtain a semi-synthetic naphtha with a similar olefins content as that of the above described fully synthetic naphtha, i.e. in the range of more than 15% or more than 20% by mass together with an aromatics content below 1% mass.
- Table 1 gives a typical composition of the two FT liquid fractions obtainable from a FT reactor.
- TABLE 1 Typical FT product after separation into two fractions (vol. % distilled) Distillation FT Condensate FT Wax Range ( ⁇ 270° C. fraction) (>270° C. fraction) C 5 -160° C. 44 3 160-270° C. 43 4 270-370° C. 13 25 370-500° C. — 40 >500° C. — 28
- Catalysts for the FT wax hydroprocessing are typically of the bifunctional type; i.e. they contain sites active for cracking and for hydrogenation.
- Catalytic metals active for hydrogenation include group VIII noble metals, such as platinum or palladium, or a sulphidcd Group VIII base metals, e.g. nickel, cobalt, which may or may not include a sulphided Group VI metal, e.g. molybdenum.
- the support for the metals can be any refractory oxide, such as silica, alumina, titania, zirconia, vanadia and other Group III, W, VA and VI oxides, alone or in combination with other refractory oxides. Alternatively, the support can partly or totally consist of zeolite. However, for this invention the preferred support is amorphous silica-alumina.
- Process conditions for hydrocracking can be varied over a wide range and are usually laboriously chosen after extensive experimentation to optimise the yield of naphtha.
- Table 2 gives a list of one such set of conditions. TABLE 2 Process conditions for hydrocracking of the FT Wax BROAD PREFERRED CONDITION RANGE RANGE Temperature, ° C. 150-450 340-400 Pressure, bar-g 10-200 30-80 Hydrogen Flow Rate, m 3 n /m 3 feed 100-2000 800-1600 Conversion of >370° C. material, mass % 30-80 50-70
- a basic process for the preparation of synthetic hydrocarbon feed is outlined in FIG. 1.
- a synthesis gas (syngas) stream 11 enters the FT reactor 1 where the synthesis gas is converted to hydrocarbons by the FT reaction.
- a waxy FT fraction is recovered in line 13 and sent to the hydroconversion unit 2 .
- the hydroprocessed product is sent to fractionator unit 3 where at least three products are recovered: hydroprocessed naphtha 17 , hydroprocessed diesel 18 , and unconverted waxy species that might be recycled to unit 2 via line 19 .
- the synthetic hydrocarbon feed of this invention may be produced either by blending streams 12 a and 17 (as shown in FIG. 1) when two fractionators are included in the process scheme or as a single stream 17 (as shown in FIG. 2) when only one fractionator is used.
- the synthetic hydrocarbon feed is a naphtha product which comprises typically a C 5 -160° C. fraction and are useful as petrochemical naphthas.
- the blending ratio for naphtha streams 12 a and 17 obtainable when including two fractionators can range from 1:2 to 2:1, typically the ratio is between 2:3 and 3:2.
- the blending ratio for naphtha 12 and hydro processed wax 15 can range from 1:10 to 10:1.
- a somewhat heavier cut, synthetic diesel is also obtainable by blending streams 12 b (olefinic distillate) and 18 (hydroconverted distillate) when two fractionators are included (FIG. 1) when two distillate fractions are recovered.
- streams 12 b olefinic distillate
- 18 hydroconverted distillate
- an equivalent product can be recovered as stream 18 as shown in FIG. 2. These two products can be used on their own or blended as a single product. All of these distillate cuts are typically recovered as 165-370° C. fractions useful as diesel fuel.
- the heavy unconverted material 19 from fractionator 3 is typically recycled to extinction to hydroconversion unit 2 .
- the residue may be used for production of high viscosity index synthetic lube oil bases.
- the synthetic hydrocarbon feed including an unhydrogenated FT fraction was prepared using the process as described above as was a fully hydroprocessed synthetic hydrocarbon feed for comparative testing.
- the characteristics of these two feeds are set out in Table 3.
- Naphtha 1 is a fully hydroprocessed FT naphtha with a 0.5% residual olefins content.
- Naphtha 2 is an olefinic FT naphtha prepared using a process scheme such as that described in FIG. 2. Its olefins content was 21.9%.
- the Cracking severity was measured by calculating the Propylene/Ethylene (P/E) mass ratio. Note that P/E ratio has an inverse relation to the cracking severity: high P/E ratios correspond to low severities (i.e. lower cracking temperatures) and lower methane co-produced.
- the lower olefins of commercial interest are ethylene, propylene and butadiene.
- the thermal cracking process also results in the production of unsaturated liquid hydrocarbons with five or more carbon atoms (C5). This product is of low commercial interest to thermal cracker operators.
- a semi-synthetic naphtha whose olefin content is similar to that of the olefinic Naphtha 2 can be prepared by blending the FT straight run Naphtha 3 fractionated from the FT condensate with a highly paraffinic conventional petrochemical naphtha.
- the composition of two of 10 these products is presented in Table 5.
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)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (11)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US10/358,129 US20040149629A1 (en) | 2003-01-31 | 2003-01-31 | Process for the preparation of and composition of a feedstock usable for the preparation of lower olefins |
CN200710089556.2A CN101033408A (zh) | 2003-01-31 | 2004-01-30 | 由合成烃原料制备低碳烯烃的热裂化方法 |
ES200550048A ES2279717B1 (es) | 2003-01-31 | 2004-01-30 | Proceso para la preparacion de una carga y composicion de dicha carga utilizable para la preparacion de olefinas inferiores. |
PCT/ZA2004/000012 WO2004067486A2 (en) | 2003-01-31 | 2004-01-30 | Process for the preparation of and composition of a feedstock usable for the preparation of lower olefins |
CN200480005586.5A CN1756828B (zh) | 2003-01-31 | 2004-01-30 | 可用作制备低碳烯烃的原料的组合物及其制备工艺 |
GB0515611A GB2412921B (en) | 2003-01-31 | 2004-01-30 | Process for the preparation of and composition of a feedstock usable for the preparation of lower olefins |
AU2004207852A AU2004207852B2 (en) | 2003-01-31 | 2004-01-30 | Process for the preparation of and composition of a feedstock usable for the preparation of lower olefins |
BR0407158-1A BRPI0407158A (pt) | 2003-01-31 | 2004-01-30 | Processo para a preparação de olefinas inferiores a partir de uma alimentação de hidrocarboneto sintético, alimentação de hidrocarboneto para um processo de craqueamento para a preparação de olefinas inferiores, processo para a preparação de uma alimentação de hidrocarboneto sintético, e, matéria-prima semi-sintética |
JP2006503927A JP4543033B2 (ja) | 2003-01-31 | 2004-01-30 | 低級オレフィンの調製のため使用可能な供給原料の調製方法および組成 |
ZA200505976A ZA200505976B (en) | 2003-01-31 | 2005-07-26 | Process for the preparation of and composition of a feedstock usable for the preparation of lower olefins |
US11/707,366 US20070203386A1 (en) | 2003-01-31 | 2007-02-15 | Process for the preparation of and composition of a feedstock usable for the preparation of lower olefins |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US10/358,129 US20040149629A1 (en) | 2003-01-31 | 2003-01-31 | Process for the preparation of and composition of a feedstock usable for the preparation of lower olefins |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US11/707,366 Division US20070203386A1 (en) | 2003-01-31 | 2007-02-15 | Process for the preparation of and composition of a feedstock usable for the preparation of lower olefins |
Publications (1)
Publication Number | Publication Date |
---|---|
US20040149629A1 true US20040149629A1 (en) | 2004-08-05 |
Family
ID=32771142
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US10/358,129 Abandoned US20040149629A1 (en) | 2003-01-31 | 2003-01-31 | Process for the preparation of and composition of a feedstock usable for the preparation of lower olefins |
US11/707,366 Abandoned US20070203386A1 (en) | 2003-01-31 | 2007-02-15 | Process for the preparation of and composition of a feedstock usable for the preparation of lower olefins |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US11/707,366 Abandoned US20070203386A1 (en) | 2003-01-31 | 2007-02-15 | Process for the preparation of and composition of a feedstock usable for the preparation of lower olefins |
Country Status (8)
Country | Link |
---|---|
US (2) | US20040149629A1 (es) |
JP (1) | JP4543033B2 (es) |
CN (2) | CN1756828B (es) |
BR (1) | BRPI0407158A (es) |
ES (1) | ES2279717B1 (es) |
GB (1) | GB2412921B (es) |
WO (1) | WO2004067486A2 (es) |
ZA (1) | ZA200505976B (es) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU2004200270B2 (en) * | 2003-01-31 | 2009-11-12 | Chevron U.S.A. Inc. | High purity olefinic naphthas for the production of ethylene and propylene |
US7150821B2 (en) | 2003-01-31 | 2006-12-19 | Chevron U.S.A. Inc. | High purity olefinic naphthas for the production of ethylene and propylene |
US7431821B2 (en) | 2003-01-31 | 2008-10-07 | Chevron U.S.A. Inc. | High purity olefinic naphthas for the production of ethylene and propylene |
KR100904297B1 (ko) * | 2007-10-26 | 2009-06-25 | 한국화학연구원 | 연속적인 2단계 촉매 반응을 이용한 합성가스로부터 경질올레핀의 제조방법 |
JP5466230B2 (ja) * | 2008-06-09 | 2014-04-09 | ソルヴェイ・スペシャルティ・ポリマーズ・イタリー・エッセ・ピ・ア | パーフルオロビニルエーテルの製造方法 |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4125566A (en) * | 1976-08-17 | 1978-11-14 | Institut Francais Du Petrole | Process for upgrading effluents from syntheses of the Fischer-Tropsch type |
US4579986A (en) * | 1984-04-18 | 1986-04-01 | Shell Oil Company | Process for the preparation of hydrocarbons |
US5371308A (en) * | 1992-08-25 | 1994-12-06 | Shell Oil Company | Process for the preparation of lower olefins |
Family Cites Families (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5519959B2 (es) * | 1972-12-05 | 1980-05-29 | ||
JPS5439003A (en) * | 1977-08-30 | 1979-03-24 | Nippon Petrochemicals Co Ltd | Thermal decomposition method oh light hydrocarbon |
DE3201457A1 (de) * | 1982-01-19 | 1983-07-28 | Basf Ag, 6700 Ludwigshafen | Verfahren zur herstellung von olefinen |
EP0584879B1 (en) * | 1992-08-25 | 1997-10-29 | Shell Internationale Researchmaatschappij B.V. | Process for the preparation of lower olefins |
US6162956A (en) * | 1998-08-18 | 2000-12-19 | Exxon Research And Engineering Co | Stability Fischer-Tropsch diesel fuel and a process for its production |
US6180842B1 (en) * | 1998-08-21 | 2001-01-30 | Exxon Research And Engineering Company | Stability fischer-tropsch diesel fuel and a process for its production |
ES2322755T3 (es) * | 1999-04-06 | 2009-06-26 | Sasol Technology (Proprietary) Limited | Combustible de nafta sintetico. |
US6497812B1 (en) * | 1999-12-22 | 2002-12-24 | Chevron U.S.A. Inc. | Conversion of C1-C3 alkanes and fischer-tropsch products to normal alpha olefins and other liquid hydrocarbons |
US6833484B2 (en) * | 2001-06-15 | 2004-12-21 | Chevron U.S.A. Inc. | Inhibiting oxidation of a Fischer-Tropsch product using petroleum-derived products |
GB0126643D0 (en) * | 2001-11-06 | 2002-01-02 | Bp Exploration Operating | Composition and process |
US7150821B2 (en) * | 2003-01-31 | 2006-12-19 | Chevron U.S.A. Inc. | High purity olefinic naphthas for the production of ethylene and propylene |
US7431821B2 (en) * | 2003-01-31 | 2008-10-07 | Chevron U.S.A. Inc. | High purity olefinic naphthas for the production of ethylene and propylene |
US6872752B2 (en) * | 2003-01-31 | 2005-03-29 | Chevron U.S.A. Inc. | High purity olefinic naphthas for the production of ethylene and propylene |
-
2003
- 2003-01-31 US US10/358,129 patent/US20040149629A1/en not_active Abandoned
-
2004
- 2004-01-30 BR BR0407158-1A patent/BRPI0407158A/pt not_active IP Right Cessation
- 2004-01-30 JP JP2006503927A patent/JP4543033B2/ja not_active Expired - Fee Related
- 2004-01-30 CN CN200480005586.5A patent/CN1756828B/zh not_active Expired - Fee Related
- 2004-01-30 WO PCT/ZA2004/000012 patent/WO2004067486A2/en active IP Right Grant
- 2004-01-30 ES ES200550048A patent/ES2279717B1/es not_active Expired - Fee Related
- 2004-01-30 CN CN200710089556.2A patent/CN101033408A/zh active Pending
- 2004-01-30 GB GB0515611A patent/GB2412921B/en not_active Expired - Fee Related
-
2005
- 2005-07-26 ZA ZA200505976A patent/ZA200505976B/en unknown
-
2007
- 2007-02-15 US US11/707,366 patent/US20070203386A1/en not_active Abandoned
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4125566A (en) * | 1976-08-17 | 1978-11-14 | Institut Francais Du Petrole | Process for upgrading effluents from syntheses of the Fischer-Tropsch type |
US4579986A (en) * | 1984-04-18 | 1986-04-01 | Shell Oil Company | Process for the preparation of hydrocarbons |
US5371308A (en) * | 1992-08-25 | 1994-12-06 | Shell Oil Company | Process for the preparation of lower olefins |
Also Published As
Publication number | Publication date |
---|---|
CN101033408A (zh) | 2007-09-12 |
ZA200505976B (en) | 2007-10-31 |
CN1756828B (zh) | 2011-03-02 |
JP4543033B2 (ja) | 2010-09-15 |
GB2412921B (en) | 2007-07-11 |
GB2412921A (en) | 2005-10-12 |
US20070203386A1 (en) | 2007-08-30 |
JP2006517254A (ja) | 2006-07-20 |
ES2279717B1 (es) | 2008-08-01 |
GB0515611D0 (en) | 2005-09-07 |
WO2004067486A3 (en) | 2004-12-09 |
BRPI0407158A (pt) | 2006-02-07 |
CN1756828A (zh) | 2006-04-05 |
WO2004067486A2 (en) | 2004-08-12 |
AU2004207852A1 (en) | 2004-08-12 |
ES2279717A1 (es) | 2007-08-16 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP3824490B2 (ja) | 合成中間留出物留分 | |
EP1171551B1 (en) | Process for producing synthetic naphtha fuel | |
US10526553B2 (en) | Method for cracking a hydrocarbon feedstock in a steam cracker unit | |
US20060201850A1 (en) | Biodegradable diesel fuel | |
US7294253B2 (en) | Process for producing middle distillates | |
US20160137933A1 (en) | Method for cracking a hydrocarbon feedstock in a steam cracker unit | |
US6709569B2 (en) | Methods for pre-conditioning fischer-tropsch light products preceding upgrading | |
EA034700B1 (ru) | Способ и установка для конверсии сырой нефти в нефтехимические продукты с повышенным выходом этилена | |
KR20160026918A (ko) | 탄화수소 공급원료로부터 경질 올레핀 및 방향족물질을 생산하는 방법 | |
JPS5857471B2 (ja) | 通常ガス状のオレフインの製法 | |
US20070203386A1 (en) | Process for the preparation of and composition of a feedstock usable for the preparation of lower olefins | |
US20110024328A1 (en) | Distillate production in a hydrocarbon synthesis process. | |
AU2005321241B2 (en) | Process for the preparation of lower olefins from heavy wax | |
US7884138B2 (en) | Process for making Fischer-Tropsch olefinic naphtha and hydrogenated distillates | |
AU2004207852B2 (en) | Process for the preparation of and composition of a feedstock usable for the preparation of lower olefins | |
CN115427539A (zh) | 轻质合成汽油的选择性生产 | |
US7727378B2 (en) | Process to prepare a Fischer-Tropsch product | |
RU2796541C2 (ru) | Способ крекинга в водородной среде для получения среднего дистиллята из легких углеводородных исходных материалов | |
RU2796569C2 (ru) | Способ крекинга в водородной среде для получения среднего дистиллята из легких углеводородных исходных материалов | |
US7744742B2 (en) | Integration of molecular redistribution and hydroisomerization processes for the production of paraffinic base oil | |
CN112166173A (zh) | 由轻质烃原料制备中间馏出物的加氢裂化方法 | |
EA040694B1 (ru) | Способ превращения сырой нефти в нефтехимические продукты |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
AS | Assignment |
Owner name: SASOL TECHNOLOGY (PTY) LTD., SOUTH AFRICA Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:KOHLER, LUIS PABLO DANCUART;REEL/FRAME:014098/0378 Effective date: 20030512 |
|
STCB | Information on status: application discontinuation |
Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION |