CA2286118A1 - Aromatics alkylation - Google Patents
Aromatics alkylation Download PDFInfo
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- CA2286118A1 CA2286118A1 CA002286118A CA2286118A CA2286118A1 CA 2286118 A1 CA2286118 A1 CA 2286118A1 CA 002286118 A CA002286118 A CA 002286118A CA 2286118 A CA2286118 A CA 2286118A CA 2286118 A1 CA2286118 A1 CA 2286118A1
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- catalyst
- alkylating agent
- crystalline material
- aromatic compound
- ray diffraction
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2/00—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms
- C07C2/54—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition of unsaturated hydrocarbons to saturated hydrocarbons or to hydrocarbons containing a six-membered aromatic ring with no unsaturation outside the aromatic ring
- C07C2/64—Addition to a carbon atom of a six-membered aromatic ring
- C07C2/66—Catalytic processes
- C07C2/68—Catalytic processes with halides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2/00—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms
- C07C2/76—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by condensation of hydrocarbons with partial elimination of hydrogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2529/00—Catalysts comprising molecular sieves
- C07C2529/04—Catalysts comprising molecular sieves having base-exchange properties, e.g. crystalline zeolites, pillared clays
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2603/00—Systems containing at least three condensed rings
- C07C2603/02—Ortho- or ortho- and peri-condensed systems
- C07C2603/04—Ortho- or ortho- and peri-condensed systems containing three rings
- C07C2603/22—Ortho- or ortho- and peri-condensed systems containing three rings containing only six-membered rings
- C07C2603/24—Anthracenes; Hydrogenated anthracenes
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2603/00—Systems containing at least three condensed rings
- C07C2603/02—Ortho- or ortho- and peri-condensed systems
- C07C2603/52—Ortho- or ortho- and peri-condensed systems containing five condensed rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2603/00—Systems containing at least three condensed rings
- C07C2603/02—Ortho- or ortho- and peri-condensed systems
- C07C2603/54—Ortho- or ortho- and peri-condensed systems containing more than five condensed rings
Abstract
Alkyl aromatic compounds are prepared by alkylating an alkylatable aromatic compound with a paraffin alkylating agent under alkylation reaction conditions in the presence of catalyst comprising synthetic porous crystalline material characterized by an X-ray diffraction pattern including interplanar d-spacings at 12.36 ~ 0.4, 11.03 ~ 0.2, 8.83 ~ 0.14, 6.18 ~ 0.12, 6.00 ~ 0.10, 4.06 ~
0.07, 3.91 ~ 0.07, and 3.42 ~ 0.06 Angstroms.
0.07, 3.91 ~ 0.07, and 3.42 ~ 0.06 Angstroms.
Description
This invention relates to a process for preparing alkyl aromatic compounds by alkylating an aromatic compound with a paraffin alkylating agent employing an alkylation catalyst comprising synthetic porous crystalline material from a particular class of materials characterized by an X-ray powder diffraction pattern including interplanar d-spacings at 12.36 ~ 0.4, 11.03 ~ 0.2, 8.83 ~ 0.14, 6.18 ~
0.12, 6.00 ~ 0.10, 4.06 ~ 0.07, 3.91 ~ 0.07, and 3.42 ~
0.06 Angstroms.
U.S. Patent Nos. 4,962,256; 4,992,606; 4,954,663;
5,001,295: and 5,043,501, each incorporated herein by reference in its entirety, teach alkylation of aromatic compounds with various alkylating agents over catalyst comprising a particular crystalline material, such as PSH-3 or MCM-22. U.S. Patent No. 4,962,256 describes preparing long chain alkylaromatic compounds by alkylating an aromatic compound with a long chain alkylating agent. U.S.
Patent No. 4,992,606 describes preparing short chain alkylaromatics by alkylating an aromatic compound with a short chain alkylating agent. U.S. Patent No. 4,954,663 teaches alkylation of phenols, and U.S. Patent No.
5,001,295 teaches alkylation of naphthalene. U.S. Patent No. 5,043,501 describes preparation of 2,6-dimethylnaphthalene. The alkylating agents taught for use in these patents are olefins such as ethylene, propylene, the butenes, and the pentenes; alcohols (inclusive of monoalcohols, dialcohols, trialcohols, etc.) such as methanol, ethanol, the propanols, the butanols, and the '30 pentanols; aldehydes such as formaldehyde, acetaldehyde, propionaldehyde, butyraldehyde, and n-valeraldehyde; and alkyl halides such as methyl chloride, ethyl chloride, the propyl chlorides, the butyl chlorides, and the pentyl chlorides, and so forth.
0.12, 6.00 ~ 0.10, 4.06 ~ 0.07, 3.91 ~ 0.07, and 3.42 ~
0.06 Angstroms.
U.S. Patent Nos. 4,962,256; 4,992,606; 4,954,663;
5,001,295: and 5,043,501, each incorporated herein by reference in its entirety, teach alkylation of aromatic compounds with various alkylating agents over catalyst comprising a particular crystalline material, such as PSH-3 or MCM-22. U.S. Patent No. 4,962,256 describes preparing long chain alkylaromatic compounds by alkylating an aromatic compound with a long chain alkylating agent. U.S.
Patent No. 4,992,606 describes preparing short chain alkylaromatics by alkylating an aromatic compound with a short chain alkylating agent. U.S. Patent No. 4,954,663 teaches alkylation of phenols, and U.S. Patent No.
5,001,295 teaches alkylation of naphthalene. U.S. Patent No. 5,043,501 describes preparation of 2,6-dimethylnaphthalene. The alkylating agents taught for use in these patents are olefins such as ethylene, propylene, the butenes, and the pentenes; alcohols (inclusive of monoalcohols, dialcohols, trialcohols, etc.) such as methanol, ethanol, the propanols, the butanols, and the '30 pentanols; aldehydes such as formaldehyde, acetaldehyde, propionaldehyde, butyraldehyde, and n-valeraldehyde; and alkyl halides such as methyl chloride, ethyl chloride, the propyl chlorides, the butyl chlorides, and the pentyl chlorides, and so forth.
It is an object of this invention to provide a process for the alkylation of an aromatic compound with a paraffin alkylating agent to produce alkyl aromatic product employing an alkylation catalyst comprising a particular, porous crystalline material characterized by an X-ray diffraction pattern including interplanar d-spacings at 12.36 ~ 0.4, 11.03 ~ 0.2, 8.83 ~ 0.14, 6.18 ~ 0.12, 6.00 ~
0.10, 4.06 ~ 0.07, 3.91 ~ 0.07, and 3.42 ~ 0.06 Angstroms.
By way of realizing the foregoing and other objects of the invention, a process for preparing alkyl aromatic compounds is provided which comprises contacting at least one alkylatable aromatic compound with at least one paraffin alkylating agent under alkylation reaction conditions and in the presence of an alkylation catalyst to provide an alkylated aromatic product possessing at least one alkyl group derived from said paraffin alkylating agent, said catalyst comprising a synthetic porous crystalline material characterized by an X-ray diffraction pattern substantially as set forth hereinafter.
The term "aromatic" in reference to the alkylatable compounds which are useful herein is to be understood in accordance with its art-recognized scope which includes alkyl substituted and unsubstituted mono- and polynuclear compounds. Compounds of an aromatic character which possess a hetero atom are also useful provided they do not act as catalyst poisons under the reaction conditions selected.
Substituted aromatic compounds which can be alkylated herein must possess at least one hydrogen atom directly bonded to the aromatic nucleus. The aromatic rings can be substituted with one or more alkyl, aryl, alkaryl, alkoxy, aryloxy, cycloalkyl, halide, and/or other groups which do not interfere with the alkylation reaction.
Suitable aromatic hydrocarbons include benzene, naphthalene, anthracene, naphthacene, perylene, coronene and phenanthrene.
,.
WO 98!46552 PCT/US97/06291 Generally the alkyl groups which can be present as substituents on the aromatic compound contain from one to about 22 carbon atoms and usually from about one to eight carbon atoms, and most usually from about one to four ,5 carbon atoms.
Suitable alkyl substituted aromatic compounds include toluene, xylene, isopropylbenzene, normal propylbenzene, alpha-methylnaphthalene, ethylbenzene, cumene, mesitylene, durene, p-cymene, butylbenzene, pseudocumene, o-diethylbenzene, m-diethylbenzene, p-diethylbenzene, isoamylbenzene, isohexylbenzene, pentaethylbenzene, pentamethylbenzene; 1,2,3,4- tetraethylbenzene; 1,2,3,5-tetramethylbenzene: 1,2,4-triethylbenzene: 1,2,3-trimethylbenzene, m-butyltoluene; p-butyltoluene; 3,5-diethyltoluene: o-ethyltoluene; p-ethyltoluene; m-propyltoluene: 4-ethyl-m-xylene; dimethylnaphthalenes;
ethylnaphthalene; 2,3-dimethylanthracene; 9-ethylanthracene; 2-methylanthracene; o-methylanthracene;
9,10-dimethylphenanthrene; and 3-methyl-phenanthrene.
Higher molecular weight alkylaromatic hydrocarbons can also be used as starting materials and include aromatic hydrocarbons such as are produced by the alkylation of aromatic hydrocarbons with olefin oligomers. Such products are frequently referred to in the art as alkylate and include hexylbenzene, nonylbenzene, dodecylbenzene, pentadecylbenzene, hexyltoluene, nonyltoluene, dodecyltoluene, pentadecytoluene, etc. Very often alkylate is obtained as a high boiling fraction in which the alkyl group attached to the aromatic nucleus varies in size from about C6 to about C12.
Reformate containing substantial quantities of benzene, toluene and/or xylene constitutes a particularly useful feed for the alkylation process of this invention.
The alkylating agents which are useful in the process of this invention generally include paraffins having from about 1 to about 14 carbon atoms, preferably from about 1 to about 8 carbon atoms. Non-limiting examples of suitable alkylating agents are propane, butanes, pentanes, hexanes, heptanes, octanes and mixtures thereof. Branched alkylating agents, especially isobutane and isopentane, are also useful herein.
In its calcined form, the synthetic porous crystalline material component employed in the catalyst composition used in the process of this invention is characterized by an X-ray diffraction pattern including the following lines:
......_...._.,..,~"."._ .. .. T.. , ." . ..
WO 98/46552 PCT/US97lOb291 TABLE A
Interplanar d-Snacina fA~ Relative Intensity. I,/Io x 12.36 ~ 0.4 M-VS
11.03 0.2 M-S
8.83 0.14 M-VS
0.10, 4.06 ~ 0.07, 3.91 ~ 0.07, and 3.42 ~ 0.06 Angstroms.
By way of realizing the foregoing and other objects of the invention, a process for preparing alkyl aromatic compounds is provided which comprises contacting at least one alkylatable aromatic compound with at least one paraffin alkylating agent under alkylation reaction conditions and in the presence of an alkylation catalyst to provide an alkylated aromatic product possessing at least one alkyl group derived from said paraffin alkylating agent, said catalyst comprising a synthetic porous crystalline material characterized by an X-ray diffraction pattern substantially as set forth hereinafter.
The term "aromatic" in reference to the alkylatable compounds which are useful herein is to be understood in accordance with its art-recognized scope which includes alkyl substituted and unsubstituted mono- and polynuclear compounds. Compounds of an aromatic character which possess a hetero atom are also useful provided they do not act as catalyst poisons under the reaction conditions selected.
Substituted aromatic compounds which can be alkylated herein must possess at least one hydrogen atom directly bonded to the aromatic nucleus. The aromatic rings can be substituted with one or more alkyl, aryl, alkaryl, alkoxy, aryloxy, cycloalkyl, halide, and/or other groups which do not interfere with the alkylation reaction.
Suitable aromatic hydrocarbons include benzene, naphthalene, anthracene, naphthacene, perylene, coronene and phenanthrene.
,.
WO 98!46552 PCT/US97/06291 Generally the alkyl groups which can be present as substituents on the aromatic compound contain from one to about 22 carbon atoms and usually from about one to eight carbon atoms, and most usually from about one to four ,5 carbon atoms.
Suitable alkyl substituted aromatic compounds include toluene, xylene, isopropylbenzene, normal propylbenzene, alpha-methylnaphthalene, ethylbenzene, cumene, mesitylene, durene, p-cymene, butylbenzene, pseudocumene, o-diethylbenzene, m-diethylbenzene, p-diethylbenzene, isoamylbenzene, isohexylbenzene, pentaethylbenzene, pentamethylbenzene; 1,2,3,4- tetraethylbenzene; 1,2,3,5-tetramethylbenzene: 1,2,4-triethylbenzene: 1,2,3-trimethylbenzene, m-butyltoluene; p-butyltoluene; 3,5-diethyltoluene: o-ethyltoluene; p-ethyltoluene; m-propyltoluene: 4-ethyl-m-xylene; dimethylnaphthalenes;
ethylnaphthalene; 2,3-dimethylanthracene; 9-ethylanthracene; 2-methylanthracene; o-methylanthracene;
9,10-dimethylphenanthrene; and 3-methyl-phenanthrene.
Higher molecular weight alkylaromatic hydrocarbons can also be used as starting materials and include aromatic hydrocarbons such as are produced by the alkylation of aromatic hydrocarbons with olefin oligomers. Such products are frequently referred to in the art as alkylate and include hexylbenzene, nonylbenzene, dodecylbenzene, pentadecylbenzene, hexyltoluene, nonyltoluene, dodecyltoluene, pentadecytoluene, etc. Very often alkylate is obtained as a high boiling fraction in which the alkyl group attached to the aromatic nucleus varies in size from about C6 to about C12.
Reformate containing substantial quantities of benzene, toluene and/or xylene constitutes a particularly useful feed for the alkylation process of this invention.
The alkylating agents which are useful in the process of this invention generally include paraffins having from about 1 to about 14 carbon atoms, preferably from about 1 to about 8 carbon atoms. Non-limiting examples of suitable alkylating agents are propane, butanes, pentanes, hexanes, heptanes, octanes and mixtures thereof. Branched alkylating agents, especially isobutane and isopentane, are also useful herein.
In its calcined form, the synthetic porous crystalline material component employed in the catalyst composition used in the process of this invention is characterized by an X-ray diffraction pattern including the following lines:
......_...._.,..,~"."._ .. .. T.. , ." . ..
WO 98/46552 PCT/US97lOb291 TABLE A
Interplanar d-Snacina fA~ Relative Intensity. I,/Io x 12.36 ~ 0.4 M-VS
11.03 0.2 M-S
8.83 0.14 M-VS
6.18 + 0.12 M-VS
6.00 0.10 W-M
4.06 + 0.07 M-S
3.91 0.07 M-VS
3.42 0.06 VS
Alternatively, it may be characterized by an X-ray diffraction pattern in its calcined form including the following lines:
TABLE B
Interplanar d-S~acina ~(A~ Relative Intensit,~y., IfIo x 30.0 + 2.2 W-M
22.1 + 1.3 W
12.36 ~ 0.4 M-VS
11.03 ~ 0.2 M-S
8.83 ~ 0.14 M-VS
6.18 ~ 0.12 M-VS
6.00 + 0.10 W-M
4.06 + 0.07 M-S
' 3.91 + 0.07 M-VS
3.42 + 0.06 VS
More specifically, the calcined form may be characterized by an X-ray diffraction pattern including the following lines:
TABr E C
Interglanar d-Spacing (Al Rel ati ve Inten~ i t~y., I f o x 12.36 0.4 M-VS
11.03 0.2 M-S
8.83 0.14 M-VS
6.86 0.14 W-M
6.18 0.12 M-VS
6.00 0.10 W-M
5.54 0.10 W-M
4.92 0.0g W
4.64 0.08 W
4.41 0.08 W-M
4.25 0.08 W
4.10 0.07 W-S
4.06 0.07 M-S
3.91 0.07 M-VS
3.75 0.06 W-M
3.56 0.06 W-M
3.42 0.06 VS
3.30 0.05 W-M
3.20 0.05 W-M
3.14 0.05 W-M
3.07 0.05 W
2.99 0.05 W
2.82 0.05 W
2.78 0.05 W
2.68 0.05 W
2.59 0.05 W
Most specifically, it may be characterized in its calcined form by an X-ray diffraction pattern including the following lines:
._~ ..._.....~..w.~.,.... r , ~nter~lanar d-S~acing~ (A~ Relative Intensity. I,Io x 30.0 + 2.2 W-M
22.1 + 1.3 W
12.36 + 0.4 M-VS
11.03 0.2 M-S
6.00 0.10 W-M
4.06 + 0.07 M-S
3.91 0.07 M-VS
3.42 0.06 VS
Alternatively, it may be characterized by an X-ray diffraction pattern in its calcined form including the following lines:
TABLE B
Interplanar d-S~acina ~(A~ Relative Intensit,~y., IfIo x 30.0 + 2.2 W-M
22.1 + 1.3 W
12.36 ~ 0.4 M-VS
11.03 ~ 0.2 M-S
8.83 ~ 0.14 M-VS
6.18 ~ 0.12 M-VS
6.00 + 0.10 W-M
4.06 + 0.07 M-S
' 3.91 + 0.07 M-VS
3.42 + 0.06 VS
More specifically, the calcined form may be characterized by an X-ray diffraction pattern including the following lines:
TABr E C
Interglanar d-Spacing (Al Rel ati ve Inten~ i t~y., I f o x 12.36 0.4 M-VS
11.03 0.2 M-S
8.83 0.14 M-VS
6.86 0.14 W-M
6.18 0.12 M-VS
6.00 0.10 W-M
5.54 0.10 W-M
4.92 0.0g W
4.64 0.08 W
4.41 0.08 W-M
4.25 0.08 W
4.10 0.07 W-S
4.06 0.07 M-S
3.91 0.07 M-VS
3.75 0.06 W-M
3.56 0.06 W-M
3.42 0.06 VS
3.30 0.05 W-M
3.20 0.05 W-M
3.14 0.05 W-M
3.07 0.05 W
2.99 0.05 W
2.82 0.05 W
2.78 0.05 W
2.68 0.05 W
2.59 0.05 W
Most specifically, it may be characterized in its calcined form by an X-ray diffraction pattern including the following lines:
._~ ..._.....~..w.~.,.... r , ~nter~lanar d-S~acing~ (A~ Relative Intensity. I,Io x 30.0 + 2.2 W-M
22.1 + 1.3 W
12.36 + 0.4 M-VS
11.03 0.2 M-S
8.83 + 0.14 M-VS
6.86 + 0.14 W-M
6.18 + 0.12 M-VS
6.00 + 0.10 W-M
5.54 + O.IO W-M
4.92 + 0.09 W
4.64 + 0.08 W
4.41 + 0.08 W-M
4.25 + 0.08 W
4.10 + 0.07 W-S
4.06 + 0.07 M-S
3.91 0.07 M-VS
3.75 + 0.06 W-M
3.56 + 0.06 W-M
3.42 + 0.06 VS
3.30 + 0.05 W-M
3.20 + 0.05 W-M
3.14 + 0.05 W-M
3.07 + 0.05 W
2.99 + 0.05 W
2.82 0.05 W
2.78 + 0.05 W
~30 2.68 0.05 W
2.59 0.05 W
These values were determined by standard techniques.
The radiation was the K-alpha doublet of copper and a _g-diffractometer equipped with a scintillation counter and an associated computer was used. The peak heights, I, and the positions as a function of 2 theta, where theta is the Bragg angle, were determined using algorithms on the computer associated with the diffractometer. From these, the relative intensities, 100 I/Io, where Io is the intensity of the strongest line or peak, and d (obs.) the interplanar spacing in Angstrom units (A), corresponding to the recorded lines, were determined. In Tables A-D, the relative intensities are given in terms of the symbols W =
weak, M = medium, S = strong, and VS = very strong. In terms of intensities, these may be generally designated as follows:
W = 0-20 M = zo-4a S = 40-60 VS = 60-100 It should be understood that these X-ray diffraction patterns are characteristic of all species of the synthetic porous crystalline material. The sodium form as well as other cationic forms reveal substantially the same pattern with some minor shifts in interplanar spacing and variation in relative intensity. Other minor variations can occur depending on the ratio of structural components, e.g., silicon to aluminum ratio of the particular sample, as well as its degree of thermal treatment. Examples of such porous crystalline materials include the PSH-3 composition of U.S. Patent 4,439,409, and MCM-22 of U.S. Patent 4,954,325.
The synthetic porous crystalline material herein can also be used in intimate combination with a hydrogenating component such as tungsten, vanadium, molybdenum, rhenium, nickel, cobalt, chromium, manganese, or a noble metal such as platinum or palladium where a hydrogenation-dehydrogenation function is to be performed. Such component can be introduced by way of co-crystallization, exchanged into the material to the extent a Group IIIA
,, _g_ element, e.g., aluminum, is in the structure, impregnated therein or intimately physically admixed therewith. Such component can be impregnated in, or on, the synthetic porous crystalline material such as, for example, by, in the case of platinum, treating the material with a solution containing a platinum metal-containing ion. Thus, suitable platinum compounds for this purpose include chloroplatinic acid, platinum halides and various compounds containing the platinum ammine complex.
The synthetic porous crystalline material for use herein, especially in its metal, hydrogen and ammonium forms, can be beneficially converted to another form by thermal treatment. This thermal treatment is generally performed by heating one of these forms at a temperature of at least about 370°C for at least 1 minute and generally not longer than 20 hours. While subatmospheric pressure can be employed for the thermal treatment, atmospheric pressure is preferred simply for reasons of convenience.
The thermal treatment can be performed at a temperature of up to about 925°C.
Prior to its use in the alkylation process of this invention, the synthetic porous crystalline material should be dehydrated, at least partially. This can be done by heating the crystalline material to a temperature in the range of from about 200°C to about 595°C in an atmosphere such as air, nitrogen, etc., and at atmospheric, subatmospheric or superatmospheric pressures for between about 30 minutes to about 48 hours. Dehydration can also be performed at room temperature merely by placing the crystalline material in a vacuum, but a longer time is required to obtain a sufficient amount of dehydration.
It may be desired to incorporate the synthetic porous crystalline material for use herein with another material ' resistant to the temperatures and other conditions employed in organic conversion processes. Such materials include active and inactive materials and synthetic or naturally occurring zeolites as well as inorganic materials such as clays, silica and/or metal oxides such as alumina. The latter may be either naturally occurring or in the form of gelatinous precipitates or gels including mixtures of silica and metal oxides. Use of a material in conjunction with the synthetic porous crystalline material, i.e., combined therewith or present during synthesis of the crystalline material, which is active, tends to change the conversion and/or selectivity of the catalyst in certain organic conversion processes. Inactive materials suitably serve as diluents to control the amount of conversion in a given process so that products can be obtained economically and orderly without employing other means for controlling the rate of reaction. These materials may be incorporated into naturally occurring clays, e.g., bentonite and kaolin, to improve the crush strength of the catalyst under commercial operating conditions. Said materials, i.e., clays, oxides, etc., function as binders for the catalyst.
It is desirable to provide a catalyst having good crush strength because in commercial use it is desirable to prevent the catalyst from breaking down into powder-like materials. These clay and/or oxide binders have been employed normally only for the purpose of improving the crush strength of the catalyst.
Naturally occurring clays which can be composited with the synthetic porous crystalline material include the montmorillonite and kaolin family, which families include the subbentonites, and the kaolins commonly known as Dixie, McNamee, Georgia and Florida clays or others in which the main mineral constituent is halloysite, kaolinite, dickite, nacrite, or anauxite. Such clays can be used in the raw state as originally mined or initially subjected to calcination, acid treatment or chemical modification.
Binders useful for compositing with the present crystalline material. also include inorganic oxides, notably alumina.
In addition to the foregoing materials, the crystalline material can be composited with a porous matrix material such as silica-alumina, silica-magnesia, silica-zirconia, silica-thoria, silica-beryllia, silica-titania as well as ternary compositions such as silica-alumina-thoria, silica-alumina-zirconia silica-alumina-magnesia and silica-magnesia-zirconia.
The relative proportions of finely divided crystalline material and inorganic oxide matrix vary widely, with the crystal content ranging from about 1 to about 90 percent by weight and more usually, particularly when the composite is prepared in the form of beads, in the range of about 2 to about 80 weight percent of the composite.
The stability of the catalyst for use herein may be increased, by, for example, combining the as-synthesized crystalline material with an alumina binder, converting the alumina-bound material to the hydrogen form, and steaming the alumina-bound material under conditions sufficient to increase the stability of the catalyst. U.S. Patent Nos.
4,663,492; 4,594,146; 4,522,929; and, 4,429,176 describe conditions for the steam stabilization of zeolite catalysts which can be utilized to steam-stabilize the present crystalline material. The steam stabilization conditions include contacting the alumina- bound material with, e.g., 5-1000 steam at a temperature of at least about 300°C
(e. g., 300-650°C) for at least one hour (e. g., 1-200 hours) at a pressure of 101-2,500 kPa. In a more particular embodiment, the alumina-bound crystalline material can be made to undergo steaming with 75-100 steam at 315°-500°C
and atmospheric pressure for 2-25 hours. In accordance with the steam stabilization treatment described in the above-mentioned patents, steaming can take place under conditions sufficient to initially increase the Alpha Value of the catalyst, the significance of which is discussed 1~, and produce a steamed catalyst having a peak Alpha Value. If desired, steaming can be continued to ' subsequently reduce the Alpha Value from the peak Alpha Value to an Alpha Value which is substantially the same as the Alpha Value of the unsteamed catalyst.
The alkylation process of this invention is conducted such that the organic reactants, i.e., the alkylatable aromatic compound and the paraffin alkylating agent, are brought into contact with the catalyst composition in a suitable reaction zone such as, for example, in a flow reactor containing a fixed bed of the catalyst composition, under effective alkylation conditions. Such conditions include a temperature of from about 0°C to about 500°C, a pressure of from about 0.2 to about 250 atmospheres, a feed weight hourly space velocity (WHSV) of from about 0.1 hr-1 to about 500 hr 1 and an alkylatable aromatic compound to alkylating agent mole ratio of from about 0.1:1 to about 50:1. The WHSV is based upon the weight of the catalyst composition employed, i.e., the total weight of active catalyst (and binder if present). Preferred reaction conditions include a temperature within the approximate range of from about 100°C to about 450°C, a pressure of from about 1 to about 25 atmospheres, a WHSV of from about 0.5 to about 100 hr-1 and an alkylatable aromatic compound to alkylating agent mole ratio of from about 0.5:1 to about 5:1. The reactants can be in either the vapor phase or the liquid phase and can be neat, i.e., free from intentional admixture or dilution with other material, ar they can be brought into contact with the zeolite catalyst composition with the aid of carrier gases or diluents such as, for example, hydrogen or nitrogen.
The alkylation process described herein can be carried out as a batch-type, semi-continuous or continuous operation utilizing a fixed or moving bed catalyst system.
A preferred embodiment entails use of a catalyst zone wherein the hydrocarbon charge is passed concurrently or countercurrently through a moving bed of particle-form catalyst. The latter, after use, is conducted to a regeneration zone where coke is burned from the catalyst in an oxygen-containing atmosphere (such as air) at elevated temperature, after which the regenerated catalyst is _.. ... ~ , .
recycled to the conversion zone for further contact with the organic reactants.
As an embodiment of the present invention, benzene levels in gasoline inventory are reduced by contacting the gasoline stream with a C1-CS paraffin stream in, for example, a 1:5 molar ratio over catalyst comprising MCM-22 at, for example, about 315°C, 500 psig, 1 hr-1 WHSV, and 0.5 HZ/paraffin molar ratio. The resultant alkylated product will contain a lower benzene level due to ring alkylation by the paraffin.
Another particularly useful embodiment of the present invention results in improved light cycle oil (LCO) quality. This is accomplished by contacting LCO with a C1-C14 paraffin in, for example, a 1:5 molar ratio over catalyst comprising MCM-22 at, for example, about 315°C, 500 psig, 1 hrl WHSV, and 2:1 H2/paraffin ratio.
Alklyation with C1-C6 paraffins will result in improved distillate cetane values while reaction with the higher molecular weight paraffins can produce a lubricant range material, potentiallly removing the need for further hydrotreating of the hydrocarbon stream.
In order to more fully illustrate the nature of the invention and the manner of practicing same, the following examples are presented.
To prepare a 65% MCM-22/35% alumina-bound catalyst for use herein, a sample of as-synthesized MCM-22 was washed with deionized water and dried at 120°C. A portion of the resultant crystals was combined with A1203 to form a mixture of 65 parts, by weight, MCM-22 and 35 parts alumina.
Sufficient water was added to this mixture to allow the resulting catalyst to be formed into extrudates. The catalyst.was calcined at 482°C in nitrogen followed by 6 hours in air at 538°C. The calcined extrudate was exchanged with 1 N NHqN03 for 2 hours at room temperature.
The exchanged catalyst was washed with deionized water and the ammonium nitrate/water wash procedure repeated twice.
After drying at 120°C, the-catalyst particles were calcined for 3 hours at 538°C in air.
F~X&MEhE 2 The catalyst of Example 1 was sized to 14/24 mesh, and 4 grams (8 cc) was loaded into a fixed-bed reactor. The catalyst was dried by flowing 150 cc/minute of nitrogen for 3 hours at 260°C and 800 psig. Isobutane was then introduced with an Isco pump at 56 grams/hour for 1 hour, and then the flow rate was reduced to 4 grams/hour. 1-Methylnaphthalene was then introduced at a rate of 4 grams/hour with a Milton Roy Mini-pump. Effective WHSV was 2 hr-1 overall. The temperature of the reactor was varied from 367°C to 454°C and the pressure was maintained at 1000 psig. Both the liquid and gas products were evaluated with a Hewlett-Packard gas chromatograph equipped with a DB-1 column. Liquid products were further characterized by gas chromatography/mass spectrometry utilizing a Finnigan TSQ70 2o Triple Quadrupole Mass Spectometer equipped with a Varian Gas Chromatograph with a DB-5 column. The results of the experimental study of this example are shown in Table E.
The results are normalized to back out the isobutane in the products.
These results show that under the experimental conditions of this study we have been able to alkylate methylnaphthalene with isobutane and also with lighter C1-C3 paraffin compounds which probably were formed from isobutane cracking and subsequent naphthalene alkylation.
r , , TABLE E
Temperature, C 367 399 427 454 Pressure, psig 1000 1000 1000 1000 %
t t d ~ ~
' S s, w 0. 00 0. 042 0. 134 0. 529 .
Co~onen ze No~a Cl-Cz C3 0.11 0.144 0.215 0.822 i-C9! 0.066 0.123 0.221 0.446 Other CQ 0.072 0.179 0.350 1.151 0 0.012 0.041 0.383 C8-Clo 0.127 0.455 0.343 0.323 Naphthalene 0.161 0.516 1.164 2.171 2-Methylnaphthalene 1.954 9.699 24.026 37.887 1-Methylnaphthalene 95.507 87.43 70.893 52.058 Cz Naphthalene 0.219 0.567 1.053 1.633 C3 Naphthalene 0.083 0.176 0.200 0.286 C9 Naphthalene 0 0.031 0.198 0.746 butyl-1-Me-Naphthalene 0.145 0.411 0.765 1.156 Unknown C11-Cls 0.557 0.200 0.383 0.391 C16+ 0 0.017 0.014 0.018 1-methyl-Naphthalene Conv. 2.238 11.445 28.181 47.270 Total methyl naphthalene Conv. (1 & 2 based) 0.700 2.056 4.266 9.296 Isobutyl-Me-Naphthalene Selectivity (1 & 2 based) 20.845 20.178 18.094 12.537
6.86 + 0.14 W-M
6.18 + 0.12 M-VS
6.00 + 0.10 W-M
5.54 + O.IO W-M
4.92 + 0.09 W
4.64 + 0.08 W
4.41 + 0.08 W-M
4.25 + 0.08 W
4.10 + 0.07 W-S
4.06 + 0.07 M-S
3.91 0.07 M-VS
3.75 + 0.06 W-M
3.56 + 0.06 W-M
3.42 + 0.06 VS
3.30 + 0.05 W-M
3.20 + 0.05 W-M
3.14 + 0.05 W-M
3.07 + 0.05 W
2.99 + 0.05 W
2.82 0.05 W
2.78 + 0.05 W
~30 2.68 0.05 W
2.59 0.05 W
These values were determined by standard techniques.
The radiation was the K-alpha doublet of copper and a _g-diffractometer equipped with a scintillation counter and an associated computer was used. The peak heights, I, and the positions as a function of 2 theta, where theta is the Bragg angle, were determined using algorithms on the computer associated with the diffractometer. From these, the relative intensities, 100 I/Io, where Io is the intensity of the strongest line or peak, and d (obs.) the interplanar spacing in Angstrom units (A), corresponding to the recorded lines, were determined. In Tables A-D, the relative intensities are given in terms of the symbols W =
weak, M = medium, S = strong, and VS = very strong. In terms of intensities, these may be generally designated as follows:
W = 0-20 M = zo-4a S = 40-60 VS = 60-100 It should be understood that these X-ray diffraction patterns are characteristic of all species of the synthetic porous crystalline material. The sodium form as well as other cationic forms reveal substantially the same pattern with some minor shifts in interplanar spacing and variation in relative intensity. Other minor variations can occur depending on the ratio of structural components, e.g., silicon to aluminum ratio of the particular sample, as well as its degree of thermal treatment. Examples of such porous crystalline materials include the PSH-3 composition of U.S. Patent 4,439,409, and MCM-22 of U.S. Patent 4,954,325.
The synthetic porous crystalline material herein can also be used in intimate combination with a hydrogenating component such as tungsten, vanadium, molybdenum, rhenium, nickel, cobalt, chromium, manganese, or a noble metal such as platinum or palladium where a hydrogenation-dehydrogenation function is to be performed. Such component can be introduced by way of co-crystallization, exchanged into the material to the extent a Group IIIA
,, _g_ element, e.g., aluminum, is in the structure, impregnated therein or intimately physically admixed therewith. Such component can be impregnated in, or on, the synthetic porous crystalline material such as, for example, by, in the case of platinum, treating the material with a solution containing a platinum metal-containing ion. Thus, suitable platinum compounds for this purpose include chloroplatinic acid, platinum halides and various compounds containing the platinum ammine complex.
The synthetic porous crystalline material for use herein, especially in its metal, hydrogen and ammonium forms, can be beneficially converted to another form by thermal treatment. This thermal treatment is generally performed by heating one of these forms at a temperature of at least about 370°C for at least 1 minute and generally not longer than 20 hours. While subatmospheric pressure can be employed for the thermal treatment, atmospheric pressure is preferred simply for reasons of convenience.
The thermal treatment can be performed at a temperature of up to about 925°C.
Prior to its use in the alkylation process of this invention, the synthetic porous crystalline material should be dehydrated, at least partially. This can be done by heating the crystalline material to a temperature in the range of from about 200°C to about 595°C in an atmosphere such as air, nitrogen, etc., and at atmospheric, subatmospheric or superatmospheric pressures for between about 30 minutes to about 48 hours. Dehydration can also be performed at room temperature merely by placing the crystalline material in a vacuum, but a longer time is required to obtain a sufficient amount of dehydration.
It may be desired to incorporate the synthetic porous crystalline material for use herein with another material ' resistant to the temperatures and other conditions employed in organic conversion processes. Such materials include active and inactive materials and synthetic or naturally occurring zeolites as well as inorganic materials such as clays, silica and/or metal oxides such as alumina. The latter may be either naturally occurring or in the form of gelatinous precipitates or gels including mixtures of silica and metal oxides. Use of a material in conjunction with the synthetic porous crystalline material, i.e., combined therewith or present during synthesis of the crystalline material, which is active, tends to change the conversion and/or selectivity of the catalyst in certain organic conversion processes. Inactive materials suitably serve as diluents to control the amount of conversion in a given process so that products can be obtained economically and orderly without employing other means for controlling the rate of reaction. These materials may be incorporated into naturally occurring clays, e.g., bentonite and kaolin, to improve the crush strength of the catalyst under commercial operating conditions. Said materials, i.e., clays, oxides, etc., function as binders for the catalyst.
It is desirable to provide a catalyst having good crush strength because in commercial use it is desirable to prevent the catalyst from breaking down into powder-like materials. These clay and/or oxide binders have been employed normally only for the purpose of improving the crush strength of the catalyst.
Naturally occurring clays which can be composited with the synthetic porous crystalline material include the montmorillonite and kaolin family, which families include the subbentonites, and the kaolins commonly known as Dixie, McNamee, Georgia and Florida clays or others in which the main mineral constituent is halloysite, kaolinite, dickite, nacrite, or anauxite. Such clays can be used in the raw state as originally mined or initially subjected to calcination, acid treatment or chemical modification.
Binders useful for compositing with the present crystalline material. also include inorganic oxides, notably alumina.
In addition to the foregoing materials, the crystalline material can be composited with a porous matrix material such as silica-alumina, silica-magnesia, silica-zirconia, silica-thoria, silica-beryllia, silica-titania as well as ternary compositions such as silica-alumina-thoria, silica-alumina-zirconia silica-alumina-magnesia and silica-magnesia-zirconia.
The relative proportions of finely divided crystalline material and inorganic oxide matrix vary widely, with the crystal content ranging from about 1 to about 90 percent by weight and more usually, particularly when the composite is prepared in the form of beads, in the range of about 2 to about 80 weight percent of the composite.
The stability of the catalyst for use herein may be increased, by, for example, combining the as-synthesized crystalline material with an alumina binder, converting the alumina-bound material to the hydrogen form, and steaming the alumina-bound material under conditions sufficient to increase the stability of the catalyst. U.S. Patent Nos.
4,663,492; 4,594,146; 4,522,929; and, 4,429,176 describe conditions for the steam stabilization of zeolite catalysts which can be utilized to steam-stabilize the present crystalline material. The steam stabilization conditions include contacting the alumina- bound material with, e.g., 5-1000 steam at a temperature of at least about 300°C
(e. g., 300-650°C) for at least one hour (e. g., 1-200 hours) at a pressure of 101-2,500 kPa. In a more particular embodiment, the alumina-bound crystalline material can be made to undergo steaming with 75-100 steam at 315°-500°C
and atmospheric pressure for 2-25 hours. In accordance with the steam stabilization treatment described in the above-mentioned patents, steaming can take place under conditions sufficient to initially increase the Alpha Value of the catalyst, the significance of which is discussed 1~, and produce a steamed catalyst having a peak Alpha Value. If desired, steaming can be continued to ' subsequently reduce the Alpha Value from the peak Alpha Value to an Alpha Value which is substantially the same as the Alpha Value of the unsteamed catalyst.
The alkylation process of this invention is conducted such that the organic reactants, i.e., the alkylatable aromatic compound and the paraffin alkylating agent, are brought into contact with the catalyst composition in a suitable reaction zone such as, for example, in a flow reactor containing a fixed bed of the catalyst composition, under effective alkylation conditions. Such conditions include a temperature of from about 0°C to about 500°C, a pressure of from about 0.2 to about 250 atmospheres, a feed weight hourly space velocity (WHSV) of from about 0.1 hr-1 to about 500 hr 1 and an alkylatable aromatic compound to alkylating agent mole ratio of from about 0.1:1 to about 50:1. The WHSV is based upon the weight of the catalyst composition employed, i.e., the total weight of active catalyst (and binder if present). Preferred reaction conditions include a temperature within the approximate range of from about 100°C to about 450°C, a pressure of from about 1 to about 25 atmospheres, a WHSV of from about 0.5 to about 100 hr-1 and an alkylatable aromatic compound to alkylating agent mole ratio of from about 0.5:1 to about 5:1. The reactants can be in either the vapor phase or the liquid phase and can be neat, i.e., free from intentional admixture or dilution with other material, ar they can be brought into contact with the zeolite catalyst composition with the aid of carrier gases or diluents such as, for example, hydrogen or nitrogen.
The alkylation process described herein can be carried out as a batch-type, semi-continuous or continuous operation utilizing a fixed or moving bed catalyst system.
A preferred embodiment entails use of a catalyst zone wherein the hydrocarbon charge is passed concurrently or countercurrently through a moving bed of particle-form catalyst. The latter, after use, is conducted to a regeneration zone where coke is burned from the catalyst in an oxygen-containing atmosphere (such as air) at elevated temperature, after which the regenerated catalyst is _.. ... ~ , .
recycled to the conversion zone for further contact with the organic reactants.
As an embodiment of the present invention, benzene levels in gasoline inventory are reduced by contacting the gasoline stream with a C1-CS paraffin stream in, for example, a 1:5 molar ratio over catalyst comprising MCM-22 at, for example, about 315°C, 500 psig, 1 hr-1 WHSV, and 0.5 HZ/paraffin molar ratio. The resultant alkylated product will contain a lower benzene level due to ring alkylation by the paraffin.
Another particularly useful embodiment of the present invention results in improved light cycle oil (LCO) quality. This is accomplished by contacting LCO with a C1-C14 paraffin in, for example, a 1:5 molar ratio over catalyst comprising MCM-22 at, for example, about 315°C, 500 psig, 1 hrl WHSV, and 2:1 H2/paraffin ratio.
Alklyation with C1-C6 paraffins will result in improved distillate cetane values while reaction with the higher molecular weight paraffins can produce a lubricant range material, potentiallly removing the need for further hydrotreating of the hydrocarbon stream.
In order to more fully illustrate the nature of the invention and the manner of practicing same, the following examples are presented.
To prepare a 65% MCM-22/35% alumina-bound catalyst for use herein, a sample of as-synthesized MCM-22 was washed with deionized water and dried at 120°C. A portion of the resultant crystals was combined with A1203 to form a mixture of 65 parts, by weight, MCM-22 and 35 parts alumina.
Sufficient water was added to this mixture to allow the resulting catalyst to be formed into extrudates. The catalyst.was calcined at 482°C in nitrogen followed by 6 hours in air at 538°C. The calcined extrudate was exchanged with 1 N NHqN03 for 2 hours at room temperature.
The exchanged catalyst was washed with deionized water and the ammonium nitrate/water wash procedure repeated twice.
After drying at 120°C, the-catalyst particles were calcined for 3 hours at 538°C in air.
F~X&MEhE 2 The catalyst of Example 1 was sized to 14/24 mesh, and 4 grams (8 cc) was loaded into a fixed-bed reactor. The catalyst was dried by flowing 150 cc/minute of nitrogen for 3 hours at 260°C and 800 psig. Isobutane was then introduced with an Isco pump at 56 grams/hour for 1 hour, and then the flow rate was reduced to 4 grams/hour. 1-Methylnaphthalene was then introduced at a rate of 4 grams/hour with a Milton Roy Mini-pump. Effective WHSV was 2 hr-1 overall. The temperature of the reactor was varied from 367°C to 454°C and the pressure was maintained at 1000 psig. Both the liquid and gas products were evaluated with a Hewlett-Packard gas chromatograph equipped with a DB-1 column. Liquid products were further characterized by gas chromatography/mass spectrometry utilizing a Finnigan TSQ70 2o Triple Quadrupole Mass Spectometer equipped with a Varian Gas Chromatograph with a DB-5 column. The results of the experimental study of this example are shown in Table E.
The results are normalized to back out the isobutane in the products.
These results show that under the experimental conditions of this study we have been able to alkylate methylnaphthalene with isobutane and also with lighter C1-C3 paraffin compounds which probably were formed from isobutane cracking and subsequent naphthalene alkylation.
r , , TABLE E
Temperature, C 367 399 427 454 Pressure, psig 1000 1000 1000 1000 %
t t d ~ ~
' S s, w 0. 00 0. 042 0. 134 0. 529 .
Co~onen ze No~a Cl-Cz C3 0.11 0.144 0.215 0.822 i-C9! 0.066 0.123 0.221 0.446 Other CQ 0.072 0.179 0.350 1.151 0 0.012 0.041 0.383 C8-Clo 0.127 0.455 0.343 0.323 Naphthalene 0.161 0.516 1.164 2.171 2-Methylnaphthalene 1.954 9.699 24.026 37.887 1-Methylnaphthalene 95.507 87.43 70.893 52.058 Cz Naphthalene 0.219 0.567 1.053 1.633 C3 Naphthalene 0.083 0.176 0.200 0.286 C9 Naphthalene 0 0.031 0.198 0.746 butyl-1-Me-Naphthalene 0.145 0.411 0.765 1.156 Unknown C11-Cls 0.557 0.200 0.383 0.391 C16+ 0 0.017 0.014 0.018 1-methyl-Naphthalene Conv. 2.238 11.445 28.181 47.270 Total methyl naphthalene Conv. (1 & 2 based) 0.700 2.056 4.266 9.296 Isobutyl-Me-Naphthalene Selectivity (1 & 2 based) 20.845 20.178 18.094 12.537
Claims (10)
1. A process for preparing alkyl aromatic compounds which comprises contacting at least one alkylatable aromatic compound with at least one paraffin alkylating agent having from about 1 to about 14 carbon atoms under alkylation reaction conditions and in the presence of an alkylation catalyst to provide an alkylated aromatic product possessing at least one alkyl group derived from said paraffin alkylating agent, said catalyst comprising synthetic porous crystalline material characterized by an X-ray diffraction pattern including interplanar d-spacing values substantially as set forth in Table A of the specification.
2. The process of claim 1 wherein the synthetic porous crystalline material is characterized by an X-ray diffraction pattern including interplanar d-spacing values substantially as set forth in Table B of the specification.
3. The process of claim 1 wherein the synthetic porous crystalline material is characterized by an X-ray diffraction pattern including interplanar d-spacing values substantially as set forth in Table C of the specification.
4. The process of claim 1 wherein the synthetic porous crystalline material is characterized by an X-ray diffraction pattern including interplanar d-spacing values substantially as set forth in Table D of the specification.
5. The process of claim 1 wherein the paraffin alkylating agent contains from about 1 to about 8 carbon atoms.
6. The process of claim 1 wherein the alkylating agent is selected from the group consisting of propane, butanes, pentanes, hexanes, heptanes, octanes, and mixtures thereof.
7. The process of claim 1 wherein the alkylatable aromatic compound is selected from the group consisting of benzene, xylene, toluene, and 1,2,3,5-tetramethylbenzene.
8. The process of claim 1 wherein the alkylatable aromatic compound is selected from the group consisting of naphthalene, anthracene, naphthacene, perylene, coronene, phenanthrene, and alkylated analogs thereof.
9. The process of claim 1 wherein the alkylation reaction conditions include a temperature of from about 0°C
to about 500°C, a pressure of from about 0.2 to about 250 atmospheres, a WHSV of from about 0.1 to 500 hr-1 and an alkylatable aromatic compound to alkylating agent mole ratio of from about 0.1:1 to 50:1.
to about 500°C, a pressure of from about 0.2 to about 250 atmospheres, a WHSV of from about 0.1 to 500 hr-1 and an alkylatable aromatic compound to alkylating agent mole ratio of from about 0.1:1 to 50:1.
10. The process of claim 1 wherein the alkylation reaction conditions include a temperature of from about 100°C to 450°C, a pressure of from about 1 to about 25 atmospheres, a WHSV of from about 0.5 to about 100 hr-1 and an alkylatable aromatic compound to alkylating agent mole ratio of from about 0.5:1 to about 5:1.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PCT/US1997/006291 WO1998046552A1 (en) | 1997-04-15 | 1997-04-15 | Aromatics alkylation |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2286118A1 true CA2286118A1 (en) | 1998-10-22 |
Family
ID=22260723
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002286118A Abandoned CA2286118A1 (en) | 1997-04-15 | 1997-04-15 | Aromatics alkylation |
Country Status (6)
| Country | Link |
|---|---|
| EP (1) | EP1015403A1 (en) |
| JP (1) | JP2001520648A (en) |
| KR (1) | KR20010006282A (en) |
| AU (1) | AU2670997A (en) |
| CA (1) | CA2286118A1 (en) |
| WO (1) | WO1998046552A1 (en) |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4524230A (en) * | 1984-06-08 | 1985-06-18 | Uop Inc. | Preparation of alkylaromatic compounds |
| US5026943A (en) * | 1988-05-09 | 1991-06-25 | Mobil Oil Corp | Catalytic conversion over catalyst comprising synthetic crystal MCM-35 |
-
1997
- 1997-04-15 JP JP54384398A patent/JP2001520648A/en active Pending
- 1997-04-15 CA CA002286118A patent/CA2286118A1/en not_active Abandoned
- 1997-04-15 KR KR1019997009366A patent/KR20010006282A/en not_active Application Discontinuation
- 1997-04-15 AU AU26709/97A patent/AU2670997A/en not_active Abandoned
- 1997-04-15 EP EP97918653A patent/EP1015403A1/en not_active Withdrawn
- 1997-04-15 WO PCT/US1997/006291 patent/WO1998046552A1/en not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| EP1015403A4 (en) | 2000-07-05 |
| AU2670997A (en) | 1998-11-11 |
| KR20010006282A (en) | 2001-01-26 |
| WO1998046552A1 (en) | 1998-10-22 |
| EP1015403A1 (en) | 2000-07-05 |
| JP2001520648A (en) | 2001-10-30 |
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