US20110190555A1 - Method for producing internal olefin, internal olefin mixture, and oil drilling fluid containing internal olefin mixture - Google Patents
Method for producing internal olefin, internal olefin mixture, and oil drilling fluid containing internal olefin mixture Download PDFInfo
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- US20110190555A1 US20110190555A1 US13/086,538 US201113086538A US2011190555A1 US 20110190555 A1 US20110190555 A1 US 20110190555A1 US 201113086538 A US201113086538 A US 201113086538A US 2011190555 A1 US2011190555 A1 US 2011190555A1
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- olefin
- internal olefin
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- carbon atoms
- zeolite catalyst
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- 150000001336 alkenes Chemical class 0.000 title claims abstract description 44
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 title claims abstract description 42
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 20
- 239000000203 mixture Substances 0.000 title claims description 17
- 238000005553 drilling Methods 0.000 title claims description 9
- 239000012530 fluid Substances 0.000 title 1
- 239000004711 α-olefin Substances 0.000 claims abstract description 71
- 239000003054 catalyst Substances 0.000 claims abstract description 40
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 claims abstract description 35
- 239000010457 zeolite Substances 0.000 claims abstract description 35
- 229910021536 Zeolite Inorganic materials 0.000 claims abstract description 34
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 26
- 238000006317 isomerization reaction Methods 0.000 claims abstract description 19
- 238000000034 method Methods 0.000 claims description 10
- 239000002199 base oil Substances 0.000 claims description 9
- 239000007788 liquid Substances 0.000 claims description 8
- 239000003921 oil Substances 0.000 claims description 8
- 239000003208 petroleum Substances 0.000 claims description 8
- 238000006384 oligomerization reaction Methods 0.000 abstract description 8
- 238000006243 chemical reaction Methods 0.000 description 26
- 230000000694 effects Effects 0.000 description 12
- 239000002994 raw material Substances 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 239000007795 chemical reaction product Substances 0.000 description 3
- 238000004821 distillation Methods 0.000 description 3
- 230000001603 reducing effect Effects 0.000 description 3
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 2
- AFFLGGQVNFXPEV-UHFFFAOYSA-N 1-decene Chemical compound CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 2
- CRSBERNSMYQZNG-UHFFFAOYSA-N 1-dodecene Chemical compound CCCCCCCCCCC=C CRSBERNSMYQZNG-UHFFFAOYSA-N 0.000 description 2
- GQEZCXVZFLOKMC-UHFFFAOYSA-N 1-hexadecene Chemical compound CCCCCCCCCCCCCCC=C GQEZCXVZFLOKMC-UHFFFAOYSA-N 0.000 description 2
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 2
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 2
- HFDVRLIODXPAHB-UHFFFAOYSA-N 1-tetradecene Chemical compound CCCCCCCCCCCCC=C HFDVRLIODXPAHB-UHFFFAOYSA-N 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- VAMFXQBUQXONLZ-UHFFFAOYSA-N n-alpha-eicosene Natural products CCCCCCCCCCCCCCCCCCC=C VAMFXQBUQXONLZ-UHFFFAOYSA-N 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- CCCMONHAUSKTEQ-UHFFFAOYSA-N octadec-1-ene Chemical compound CCCCCCCCCCCCCCCCC=C CCCMONHAUSKTEQ-UHFFFAOYSA-N 0.000 description 2
- GNRSAWUEBMWBQH-UHFFFAOYSA-N oxonickel Chemical compound [Ni]=O GNRSAWUEBMWBQH-UHFFFAOYSA-N 0.000 description 2
- GGQQNYXPYWCUHG-RMTFUQJTSA-N (3e,6e)-deca-3,6-diene Chemical compound CCC\C=C\C\C=C\CC GGQQNYXPYWCUHG-RMTFUQJTSA-N 0.000 description 1
- 229940106006 1-eicosene Drugs 0.000 description 1
- FIKTURVKRGQNQD-UHFFFAOYSA-N 1-eicosene Natural products CCCCCCCCCCCCCCCCCC=CC(O)=O FIKTURVKRGQNQD-UHFFFAOYSA-N 0.000 description 1
- 241000251468 Actinopterygii Species 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- JYIBXUUINYLWLR-UHFFFAOYSA-N aluminum;calcium;potassium;silicon;sodium;trihydrate Chemical compound O.O.O.[Na].[Al].[Si].[K].[Ca] JYIBXUUINYLWLR-UHFFFAOYSA-N 0.000 description 1
- UNYSKUBLZGJSLV-UHFFFAOYSA-L calcium;1,3,5,2,4,6$l^{2}-trioxadisilaluminane 2,4-dioxide;dihydroxide;hexahydrate Chemical compound O.O.O.O.O.O.[OH-].[OH-].[Ca+2].O=[Si]1O[Al]O[Si](=O)O1.O=[Si]1O[Al]O[Si](=O)O1 UNYSKUBLZGJSLV-UHFFFAOYSA-L 0.000 description 1
- 238000004523 catalytic cracking Methods 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 229910052676 chabazite Inorganic materials 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229910001603 clinoptilolite Inorganic materials 0.000 description 1
- 239000013065 commercial product Substances 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 229940069096 dodecene Drugs 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 229910052675 erionite Inorganic materials 0.000 description 1
- 239000012013 faujasite Substances 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 239000010687 lubricating oil Substances 0.000 description 1
- 239000002808 molecular sieve Substances 0.000 description 1
- 229910052680 mordenite Inorganic materials 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 238000010926 purge Methods 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 238000004513 sizing Methods 0.000 description 1
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K8/00—Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
- C09K8/02—Well-drilling compositions
- C09K8/32—Non-aqueous well-drilling compositions, e.g. oil-based
- C09K8/34—Organic liquids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C5/00—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms
- C07C5/22—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by isomerisation
- C07C5/23—Rearrangement of carbon-to-carbon unsaturated bonds
- C07C5/25—Migration of carbon-to-carbon double bonds
- C07C5/2506—Catalytic processes
- C07C5/2518—Catalytic processes with crystalline alumino-silicates, e.g. molecular sieves
Definitions
- the present invention relates to a method for producing an internal olefin by isomerizing an ⁇ -olefin having from 16 to 18 carbon atoms, to an internal olefin mixture and to a base oil for petroleum drilling oils containing an internal olefin mixture.
- ⁇ -olefins having 14 carbon atoms are used as a base oil for petroleum drilling oils, when released in the environment, the ⁇ -olefins having 14 carbon atoms exhibit fish toxicity, and therefore, in the case of a submarine oilfield, it is considered to be preferable to use ⁇ -olefins having 16 or more carbon atoms.
- the ⁇ -olefins having 16 or more carbon atoms are inferior in fluidity to the ⁇ -olefins having 14 carbon atoms, it is necessary that they are internally isomerized to improve the fluidity.
- Patent Document 1 U.S. Pat. No. 6,054,629
- Patent Document 2 U.S. Pat. No. 6,281,404
- the present invention has been made and is aimed to provide a method for producing an internal olefin by stably isomerizing an ⁇ -olefin by using an inexpensive zeolite catalyst while preventing an oligomerization reaction.
- the present inventors made extensive and intensive investigations. As a result, it has been found that by circulating a starting ⁇ -olefin into a zeolite catalyst bed before starting an isomerization reaction, the oligomerization reaction activity can be largely reduced and that by the foregoing circulation, an internal olefin with more excellent fluidity can be produced without performing distillation.
- the present invention has been accomplished on the basis of such knowledge.
- the present invention is to provide a method for producing an internal olefin, an internal olefin mixture and a base oil for petroleum drilling oils containing an internal olefin mixture.
- a method for producing an internal olefin comprising a step of isomerizing an ⁇ -olefin having from 16 to 18 carbon atoms by passing through a zeolite catalyst bed, an ⁇ -olefin having from 16 to 18 carbon atoms being circulated through and brought into contact with the zeolite catalyst bed before starting the isomerization reaction.
- a base oil for petroleum drilling oils containing the internal olefin mixture having from 16 to 18 carbon atoms as recited in (7) above.
- the oligomerization reaction activity of the zeolite catalyst bed can be largely reduced, and an internal olefin with good fluidity can be produced stably with good efficiency and advantageously from the industrial viewpoint.
- the starting ⁇ -olefin of the present invention is an ⁇ -olefin having from 16 to 18 carbon atoms.
- a proportion (mass ratio) of an ⁇ -olefin having 16 carbon atoms to an ⁇ -olefin having 18 carbon atoms in the starting ⁇ -olefin is not particularly limited, it is usually from 20/80 to 35/65, and preferably from 25/75 to 32/68.
- This ⁇ -olefin having from 16 to 18 carbon atoms can be obtained by distilling a low polymer which is preferably resulted from lowly polymerizing ethylene by using a Ziegler type catalyst.
- This oligomer is a mixture of 1-butene, 1-hexene, 1-octene, 1-decene, 1-dodecene, 1-tetradecene, 1-hexadecene, 1-octadecene, 1-eicosene, and the like.
- the ⁇ -olefin which is used in the present invention can also be obtained by distilling an ⁇ -olefin obtained from a catalytic cracking apparatus or the like.
- Examples of the zeolite catalyst which is used in the present invention include natural zeolites and synthetic zeolites.
- Examples of the natural zeolite include chabazite, mordenite, erionite, faujasite, and clinoptilolite.
- Examples of the synthetic zeolite include an A type, a B type, an X type, a Y type, an omega type, and an MFI type. Of these, an MFI type is preferable; and ZSM-5 or the like is suitable as the MFI type.
- a proton type zeolite resulting from substitution of a part or the whole of cations is especially preferable; and above all, proton-substituted H-ZSM-5 is preferable.
- the starting ⁇ -olefin having from 16 to 18 carbon atoms is circulated through and brought into contact with the zeolite catalyst bed.
- the amount of the ⁇ -olefin which is used for this circulation is preferably from 1 to 20 times, and more preferably from 3 to 10 times of the zeolite catalyst by volume.
- the amount of the ⁇ -olefin which is used for the circulation is 1 or more times of the zeolite catalyst by volume, an effect for reducing the oligomerization reaction activity of this catalyst is exhibited; and when the amount of the ⁇ -olefin is 20 times or less, it is economically practical.
- an LHSV (liquid hourly space velocity) of the ⁇ -olefin during the foregoing circulation is usually from approximately 0.1 to 10 h -1 , and preferably from 1 to 5 h -1 .
- a temperature of the zeolite catalyst bed at the circulation of the ⁇ -olefin is usually from approximately 70 to 180° C., and preferably from 100 to 160° C. From the standpoint of a good balance between the reducing effect of the oligomer reaction activity of the zeolite catalyst bed and the economy, the circulation time of the ⁇ -olefin is usually from approximately 1 to 100 hours, and preferably from 4 to 48 hours.
- the ⁇ -olefin having from 16 to 18 carbon atoms is isomerized by passing through the zeolite catalyst bed having an ⁇ -olefin circulated therethrough and brought into contact therewith, thereby producing an internal olefin.
- the ⁇ -olefin used for the foregoing circulation can be used as a raw material.
- a temperature of the isomerization reaction is usually from approximately 70 to 180° C., and preferably from 100 to 160° C.
- a reaction mode is not particularly limited and may be any of a fixed bed circulation type or a batch type (including a continuous type stirring tank).
- a pressure is usually from approximately atmospheric pressure to 5 MPa, and preferably from atmospheric pressure to 1 MPa.
- an LHSV (liquid hourly space velocity) of the ⁇ -olefin is usually selected from the range of from approximately 0.1 to 10 h -1 , and preferably from 1 to 4 h -1 .
- the amount of used amount of the zeolite catalyst is usually in the range of from 1 to 60 parts by mass, preferably from 10 to 50 parts by mass, and more preferably from 20 to 40 parts by mass based on 100 parts by mass of the starting ⁇ -olefin.
- a reaction time varies depending upon the reaction temperature and the desired ⁇ -olefin conversion rate and cannot be determined indiscriminately, it is usually from approximately 30 minutes to 20 hours, and preferably from approximately 1 to 10 hours.
- the ⁇ -olefin can be internally isomerized at a conversion rate of 90% or more under a relatively mild condition. Moreover, since it is possible to prevent the deterioration of the catalyst and undesired side-reactions such as skeletal isomerization reaction and oligomerization reaction, the desired internal olefin is selectively obtained.
- the zeolite catalyst which is used in the present invention is generally inexpensive, it is possible to design a sufficiently economical process even on the assumption that the catalyst is exchanged.
- the present invention is to provide an internal olefin mixture obtained by the foregoing method and a base oil for petroleum drilling oils containing this internal olefin mixture.
- a stainless steel-made reaction column having a diameter of 12 mm (length: 1.1 m, inside diameter: 10 mm) was filled with 50 mL of HMFI-90 (a proton type MFI zeolite catalyst, manufactured by Sud-Chemie), and the inside of the reaction column was purged with nitrogen.
- HMFI-90 a proton type MFI zeolite catalyst, manufactured by Sud-Chemie
- a mixture of 70% by mass of an ⁇ -olefin having 16 carbon atoms (C16) and 30% by mass of an ⁇ -olefin having 18 carbon atoms (C18) was fed by an up-flow at 100 mL/h into this reactor.
- the reaction was continued while increasing the reaction temperature as the catalyst activity decreases, such that the conversion rate of the ⁇ -olefin became 93 to 95% or more. After 24 hours, the catalyst activity was stable, and the reaction temperature at that time was 130° C.
- the reaction temperature was 130° C.; and the isomerization conversion rate of a double bond was 94% for the C16 ⁇ -olefin and 93% for the C18 ⁇ -olefin, respectively.
- an oligomer concentration in the formed liquid was 2.1% by mass.
- the kinematic viscosity of the resulting internal olefin was measured at 0° C. by using a Cannon-Fenske viscometer, thereby evaluating the fluidity.
- the foregoing circulation was stopped; subsequent to the foregoing 300 mL ⁇ -olefin mixture, the same ⁇ -olefin mixture was fed by an up-flow at 100 mL/h; and the reaction was continued while increasing the reaction temperature as the catalyst activity decreases such that the conversion rate of the ⁇ -olefin became 93 to 95% or more. After 24 hours, the catalyst activity was stable, and the reaction temperature at that time was 135° C.
- the internal olefin obtained by the producing method of the present invention is good in fluidity and suitable for applications such as a base oil for petroleum drilling oils.
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Crystallography & Structural Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
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- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
A method for producing an internal olefin by stably isomerizing an α-olefin by using an inexpensive zeolite catalyst while preventing an oligomerization reaction is provided. The method for producing an internal olefin comprises a step of isomerizing an α-olefin having from 16 to 18 carbon atoms by passing through a zeolite catalyst bed, wherein the α-olefin having from 16 to 18 carbon atoms is circulated through and brought into contact with the zeolite catalyst bed before starting the isomerization reaction.
Description
- The present invention relates to a method for producing an internal olefin by isomerizing an α-olefin having from 16 to 18 carbon atoms, to an internal olefin mixture and to a base oil for petroleum drilling oils containing an internal olefin mixture.
- Internal olefins have hitherto been used for various applications, concretely a base oil for petroleum drilling oils, a raw material of detergents, a raw material of paper sizing agents, a base oil or raw material of lubricating oils, a raw material of chemical products, and the like. For example, though α-olefins having 14 carbon atoms are used as a base oil for petroleum drilling oils, when released in the environment, the α-olefins having 14 carbon atoms exhibit fish toxicity, and therefore, in the case of a submarine oilfield, it is considered to be preferable to use α-olefins having 16 or more carbon atoms. However, since the α-olefins having 16 or more carbon atoms are inferior in fluidity to the α-olefins having 14 carbon atoms, it is necessary that they are internally isomerized to improve the fluidity.
- In the case of performing an internal isomerization reaction of an α-olefin, it is important to prevent the formation of branched olefins. Similar to the problems in the field of surfactants, this is because the branched olefins are poor in biodegradability so that they remain in the environment over a long period of time. Then, there have been filed some patent applications regarding technologies for preventing a skeletal isomerization reaction so that only an internal isomerization reaction of an α-olefin is selectively performed. Though there is no definite index on how extent the skeletal isomerization should be prevented, for example, it is disclosed that a rate of skeletal isomerization reaction is controlled to less than 5% (see, for example, Patent Document 1).
- In the internal isomerization reaction of an α-olefin using a zeolite catalyst, as a method for preventing the skeletal isomerization reaction, there are disclosed a method for using a pentasil zeolite catalyst containing from 1 to 10% by weight of nickel monoxide as a promoter (see, for example, Patent Document 1); and a method for using an alumina-phosphate-containing molecular sieve with one-dimensional pores having a diameter of from 3.8 to 5.0 angstroms as a catalyst (see, for example, Patent Document 2).
- In the case of performing the internal isomerization reaction of an α-olefin, another important point resides in the matter that an oligomer is not formed in the reaction. When an oligomer increases, it is easily supposed that the fluidity of a formed internal olefin is deteriorated, and it is desired to suppress the formation of an oligomer as much as possible.
- In claim 8 of Patent Document 1, it is described that a residual α-olefin is controlled to less than 5%, and in Example 3 thereof, it is actually proven that in isomerizing an α-olefin having 18 carbon atoms, the amount of formation of an olefin having 36 carbon atoms is controlled at not more than 4%.
- In the light of the above, in order to improve the fluidity of an internal olefin, it is devised to reduce an oligomer at a 1% unit. However, it is still hard to say that the reduction of an oligomer is sufficient, and there may be the case where for the purpose of making the concentration of an oligomer low, the reaction product liquid must be further distilled.
- Accordingly, a method for producing an internal olefin by stably isomerizing an α-olefin while preventing an oligomerization reaction is desired.
- Patent Document 1: U.S. Pat. No. 6,054,629
- Patent Document 2: U.S. Pat. No. 6,281,404
- Under the foregoing circumstances, the present invention has been made and is aimed to provide a method for producing an internal olefin by stably isomerizing an α-olefin by using an inexpensive zeolite catalyst while preventing an oligomerization reaction.
- In order to solve the foregoing problems, the present inventors made extensive and intensive investigations. As a result, it has been found that by circulating a starting α-olefin into a zeolite catalyst bed before starting an isomerization reaction, the oligomerization reaction activity can be largely reduced and that by the foregoing circulation, an internal olefin with more excellent fluidity can be produced without performing distillation. The present invention has been accomplished on the basis of such knowledge.
- That is, the present invention is to provide a method for producing an internal olefin, an internal olefin mixture and a base oil for petroleum drilling oils containing an internal olefin mixture.
- (1) A method for producing an internal olefin, comprising a step of isomerizing an α-olefin having from 16 to 18 carbon atoms by passing through a zeolite catalyst bed, an α-olefin having from 16 to 18 carbon atoms being circulated through and brought into contact with the zeolite catalyst bed before starting the isomerization reaction.
- (2) The method for producing an internal olefin as recited in (1) above, wherein the zeolite catalyst is an MFI type zeolite.
- (3) The method for producing an internal olefin as recited in (1) or (2) above, wherein the total amount of the α-olefin to be circulated is from 1 to 20 times of the zeolite catalyst by volume.
- (4) The method for producing an internal olefin as recited in any one of (1) to (3) above, wherein an LHSV (liquid hourly space velocity) of the α-olefin to be circulated is from 0.1 to 10 h-1.
- (5) The method for producing an internal olefin as recited in any one of (1) to (4) above, wherein a temperature of the catalyst bed at the circulation of the α-olefin is from 70 to 180° C.
- (6) The method for producing an internal olefin as recited in any one of (1) to (5) above, wherein a circulation time of the α-olefin is from 1 to 100 hours.
- (7) An internal olefin mixture having from 16 to 18 carbon atoms obtained by the method recited in any one of (1) to (6) above.
- (8) A base oil for petroleum drilling oils containing the internal olefin mixture having from 16 to 18 carbon atoms as recited in (7) above.
- According to the present invention, the oligomerization reaction activity of the zeolite catalyst bed can be largely reduced, and an internal olefin with good fluidity can be produced stably with good efficiency and advantageously from the industrial viewpoint.
- The starting α-olefin of the present invention is an α-olefin having from 16 to 18 carbon atoms. Though a proportion (mass ratio) of an α-olefin having 16 carbon atoms to an α-olefin having 18 carbon atoms in the starting α-olefin is not particularly limited, it is usually from 20/80 to 35/65, and preferably from 25/75 to 32/68.
- This α-olefin having from 16 to 18 carbon atoms can be obtained by distilling a low polymer which is preferably resulted from lowly polymerizing ethylene by using a Ziegler type catalyst. This oligomer is a mixture of 1-butene, 1-hexene, 1-octene, 1-decene, 1-dodecene, 1-tetradecene, 1-hexadecene, 1-octadecene, 1-eicosene, and the like.
- In addition, the α-olefin which is used in the present invention can also be obtained by distilling an α-olefin obtained from a catalytic cracking apparatus or the like.
- Examples of the zeolite catalyst which is used in the present invention include natural zeolites and synthetic zeolites. Examples of the natural zeolite include chabazite, mordenite, erionite, faujasite, and clinoptilolite. Examples of the synthetic zeolite include an A type, a B type, an X type, a Y type, an omega type, and an MFI type. Of these, an MFI type is preferable; and ZSM-5 or the like is suitable as the MFI type. A proton type zeolite resulting from substitution of a part or the whole of cations is especially preferable; and above all, proton-substituted H-ZSM-5 is preferable.
- In the method for producing an internal olefin of the present invention, before starting the isomerization reaction, the starting α-olefin having from 16 to 18 carbon atoms is circulated through and brought into contact with the zeolite catalyst bed. The amount of the α-olefin which is used for this circulation is preferably from 1 to 20 times, and more preferably from 3 to 10 times of the zeolite catalyst by volume. When the amount of the α-olefin which is used for the circulation is 1 or more times of the zeolite catalyst by volume, an effect for reducing the oligomerization reaction activity of this catalyst is exhibited; and when the amount of the α-olefin is 20 times or less, it is economically practical.
- Considering the reducing effect of the oligomer reaction activity of the zeolite catalyst bed and the like, an LHSV (liquid hourly space velocity) of the α-olefin during the foregoing circulation is usually from approximately 0.1 to 10 h-1, and preferably from 1 to 5 h-1.
- A temperature of the zeolite catalyst bed at the circulation of the α-olefin is usually from approximately 70 to 180° C., and preferably from 100 to 160° C. From the standpoint of a good balance between the reducing effect of the oligomer reaction activity of the zeolite catalyst bed and the economy, the circulation time of the α-olefin is usually from approximately 1 to 100 hours, and preferably from 4 to 48 hours.
- In the present invention, as described previously, the α-olefin having from 16 to 18 carbon atoms is isomerized by passing through the zeolite catalyst bed having an α-olefin circulated therethrough and brought into contact therewith, thereby producing an internal olefin. In that case, the α-olefin used for the foregoing circulation can be used as a raw material. A temperature of the isomerization reaction is usually from approximately 70 to 180° C., and preferably from 100 to 160° C.
- A reaction mode is not particularly limited and may be any of a fixed bed circulation type or a batch type (including a continuous type stirring tank). A pressure is usually from approximately atmospheric pressure to 5 MPa, and preferably from atmospheric pressure to 1 MPa. In the case where the reaction mode is a fixed bed circulation type, considering an α-olefin conversion rate and productivity, an LHSV (liquid hourly space velocity) of the α-olefin is usually selected from the range of from approximately 0.1 to 10 h-1, and preferably from 1 to 4 h-1.
- Also, in the case where the reaction mode is a batch type, the amount of used amount of the zeolite catalyst is usually in the range of from 1 to 60 parts by mass, preferably from 10 to 50 parts by mass, and more preferably from 20 to 40 parts by mass based on 100 parts by mass of the starting α-olefin. In that case, though a reaction time varies depending upon the reaction temperature and the desired α-olefin conversion rate and cannot be determined indiscriminately, it is usually from approximately 30 minutes to 20 hours, and preferably from approximately 1 to 10 hours.
- In the light of the above, by using the zeolite catalyst having the starting α-olefin circulated therethrough and brought into contact therewith before starting the isomerization reaction, the α-olefin can be internally isomerized at a conversion rate of 90% or more under a relatively mild condition. Moreover, since it is possible to prevent the deterioration of the catalyst and undesired side-reactions such as skeletal isomerization reaction and oligomerization reaction, the desired internal olefin is selectively obtained.
- Also, since commercial product can be obtained without performing distillation purification of the reaction product liquid, a distillation column for the removal of the oligomerization reaction product or the like becomes unnecessary, and therefore the method is highly economical. Also, since the zeolite catalyst which is used in the present invention is generally inexpensive, it is possible to design a sufficiently economical process even on the assumption that the catalyst is exchanged.
- Also, the present invention is to provide an internal olefin mixture obtained by the foregoing method and a base oil for petroleum drilling oils containing this internal olefin mixture.
- Next, the present invention is described below in more detail with reference to the Examples. However, it should be construed that the present invention is not limited to these Examples in any way.
- A stainless steel-made reaction column having a diameter of 12 mm (length: 1.1 m, inside diameter: 10 mm) was filled with 50 mL of HMFI-90 (a proton type MFI zeolite catalyst, manufactured by Sud-Chemie), and the inside of the reaction column was purged with nitrogen. A mixture of 70% by mass of an α-olefin having 16 carbon atoms (C16) and 30% by mass of an α-olefin having 18 carbon atoms (C18) was fed by an up-flow at 100 mL/h into this reactor. The reaction was continued while increasing the reaction temperature as the catalyst activity decreases, such that the conversion rate of the α-olefin became 93 to 95% or more. After 24 hours, the catalyst activity was stable, and the reaction temperature at that time was 130° C.
- At a point of time of elapsing 48 hours since starting the feed of the α-olefin, the reaction temperature was 130° C.; and the isomerization conversion rate of a double bond was 94% for the C16 α-olefin and 93% for the C18 α-olefin, respectively. Also, an oligomer concentration in the formed liquid was 2.1% by mass. In addition, the kinematic viscosity of the resulting internal olefin was measured at 0° C. by using a Cannon-Fenske viscometer, thereby evaluating the fluidity. These results are shown in Table 1.
- The same operations up to purging the inside of the reaction column with nitrogen as in Comparative Example 1 were repeated. Thereafter, 300 mL of a mixture of 70% by mass of a C16 α-olefin and 30% by mass of a C18 α-olefin was circulated and contacted by an up-flow at 100 mL/hr for 24 hours in the reactor. During this circulation, the LHSV of the α-olefin was 2 h-1, and the temperature of the zeolite catalyst bed was 150° C.
- Next, the foregoing circulation was stopped; subsequent to the foregoing 300 mL α-olefin mixture, the same α-olefin mixture was fed by an up-flow at 100 mL/h; and the reaction was continued while increasing the reaction temperature as the catalyst activity decreases such that the conversion rate of the α-olefin became 93 to 95% or more. After 24 hours, the catalyst activity was stable, and the reaction temperature at that time was 135° C.
- After stopping the circulation, at a point of time of elapsing 48 hours since starting the feed of the α-olefin, the reaction temperature was 135° C.; and the isomerization conversion rate of a double bond was 95% for the C16 α-olefin and 93% for the C18 α-olefin, respectively. Also, an oligomer concentration in the formed liquid was 1.2% by mass, and the oligomer formation activity was reduced by half as compared with Comparative Example 1. In addition, the fluidity of the obtained internal olefin was evaluated in the same method as described above. These results are shown in Table 1.
-
TABLE 1 Isomerization Oligomer conversion rate (%) concentration C16 α-olefin C18 α-olefin (% by mass) Fluidity Example 1 95 93 1.2 Good Comparative 94 93 2.1 Poor Example 1 (Note) Fluidity: Good: The kinematic viscosity at 0° C. is less than 8.0 mm2/s. Poor: The kinematic viscosity at 0° C. is 8.0 mm2/s or more. - The internal olefin obtained by the producing method of the present invention is good in fluidity and suitable for applications such as a base oil for petroleum drilling oils.
Claims (8)
1. A method for producing an internal olefin, comprising a step of isomerizing an α-olefin having from 16 to 18 carbon atoms by passing through a zeolite catalyst bed, an α-olefin having from 16 to 18 carbon atoms being circulated through and brought into contact with the zeolite catalyst bed before starting the isomerization reaction.
2. The method for producing an internal olefin according to claim 1 , wherein the zeolite catalyst is an MFI type zeolite.
3. The method for producing an internal olefin according to claim 1 , wherein the total amount of the α-olefin to be circulated is from 1 to 20 times of the zeolite catalyst by volume.
4. The method for producing an internal olefin according to claim 1 , wherein an LHSV (liquid hourly space velocity) of the α-olefin to be circulated is from 0.1 to 10 h-1.
5. The method for producing an internal olefin according to claim 1 , wherein the temperature of the catalyst bed at the circulation of the α-olefin is from 70 to 180° C.
6. The method for producing an internal olefin according to claim 1 , wherein the circulation time of the α-olefin is from 1 to 100 hours.
7. An internal olefin mixture having from 16 to 18 carbon atoms obtained by the method according to claim 1 .
8. A base oil for petroleum drilling oils containing the internal olefin mixture having from 16 to 18 carbon atoms according to claim 7 .
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US13/086,538 US20110190555A1 (en) | 2005-01-12 | 2011-04-14 | Method for producing internal olefin, internal olefin mixture, and oil drilling fluid containing internal olefin mixture |
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JP2005004828A JP4764013B2 (en) | 2005-01-12 | 2005-01-12 | Method for producing internal olefin, internal olefin mixture, and petroleum drilling base oil containing internal olefin mixture |
JP2005-004828 | 2005-01-12 | ||
PCT/JP2005/024029 WO2006075526A1 (en) | 2005-01-12 | 2005-12-28 | Method for producing internal olefin, internal olefin mixture, and oil drilling fluid containing internal olefin mixture |
US81372707A | 2007-07-11 | 2007-07-11 | |
US13/086,538 US20110190555A1 (en) | 2005-01-12 | 2011-04-14 | Method for producing internal olefin, internal olefin mixture, and oil drilling fluid containing internal olefin mixture |
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PCT/JP2005/024029 Continuation WO2006075526A1 (en) | 2005-01-12 | 2005-12-28 | Method for producing internal olefin, internal olefin mixture, and oil drilling fluid containing internal olefin mixture |
US81372707A Continuation | 2005-01-12 | 2007-07-11 |
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US13/086,538 Abandoned US20110190555A1 (en) | 2005-01-12 | 2011-04-14 | Method for producing internal olefin, internal olefin mixture, and oil drilling fluid containing internal olefin mixture |
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EP (1) | EP1842840B1 (en) |
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WO2019118228A1 (en) | 2017-12-14 | 2019-06-20 | Exxonmobil Chemical Patents Inc. | Processes for isomerizing alpha olefins |
US11332420B2 (en) | 2017-12-14 | 2022-05-17 | Exxonmobil Chemical Patents Inc. | Processes for isomerizing alpha olefins |
US11261141B2 (en) | 2017-12-14 | 2022-03-01 | Exxonmobil Chemical Patents Inc. | Processes for isomerizing alpha olefins |
WO2023008464A1 (en) * | 2021-07-27 | 2023-02-02 | 花王株式会社 | Method for producing internal olefin, method for producing internal olefin sulfonate, and low-temperature stabilization method |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
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US5087793A (en) * | 1988-09-27 | 1992-02-11 | Naoki Akiyama | Process for preparing inner olefines |
US6054629A (en) * | 1998-07-15 | 2000-04-25 | Chevron Chemical Company Llc | Method of isomerizing alpha-olefins to linear internal olefins with minimal skeletal isomerization using nickel supported on silica/alumina catalysts |
US7718580B2 (en) * | 2004-09-03 | 2010-05-18 | Idemitsu Kosan Co., Ltd. | Internal-olefin composition and base oil comprising the composition for oil drilling |
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JPH10167992A (en) * | 1996-12-06 | 1998-06-23 | Nippon Shokubai Co Ltd | Isomerization of olefin and catalyst used therefor |
US6407302B1 (en) * | 1999-11-04 | 2002-06-18 | Bp Corporation North America Inc. | Isomerization process of a mixture containing vinyl and vinylidene olefins |
JP2004285000A (en) * | 2003-03-24 | 2004-10-14 | Idemitsu Petrochem Co Ltd | Production method for internal olefin |
JP4769422B2 (en) * | 2004-02-27 | 2011-09-07 | 出光興産株式会社 | Method for producing internal olefin |
JP4806176B2 (en) | 2004-09-03 | 2011-11-02 | 出光興産株式会社 | Internal olefin composition and petroleum drilling base oil containing the composition |
-
2005
- 2005-01-12 JP JP2005004828A patent/JP4764013B2/en not_active Expired - Fee Related
- 2005-12-28 US US11/813,727 patent/US7956229B2/en active Active
- 2005-12-28 CA CA2593310A patent/CA2593310C/en active Active
- 2005-12-28 EP EP05844846.5A patent/EP1842840B1/en not_active Not-in-force
- 2005-12-28 WO PCT/JP2005/024029 patent/WO2006075526A1/en active Application Filing
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Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5087793A (en) * | 1988-09-27 | 1992-02-11 | Naoki Akiyama | Process for preparing inner olefines |
US6054629A (en) * | 1998-07-15 | 2000-04-25 | Chevron Chemical Company Llc | Method of isomerizing alpha-olefins to linear internal olefins with minimal skeletal isomerization using nickel supported on silica/alumina catalysts |
US7718580B2 (en) * | 2004-09-03 | 2010-05-18 | Idemitsu Kosan Co., Ltd. | Internal-olefin composition and base oil comprising the composition for oil drilling |
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WO2006075526A1 (en) | 2006-07-20 |
CA2593310A1 (en) | 2006-07-20 |
EP1842840A4 (en) | 2008-10-08 |
US7956229B2 (en) | 2011-06-07 |
JP2006193442A (en) | 2006-07-27 |
CA2593310C (en) | 2013-05-14 |
JP4764013B2 (en) | 2011-08-31 |
EP1842840A1 (en) | 2007-10-10 |
US20080167510A1 (en) | 2008-07-10 |
EP1842840B1 (en) | 2016-05-04 |
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