BACKGROUND OF THE INVENTION

[0002 j A variety of industrial processes are known for conversion of low boiling carbon-containing compounds to higher value products. One such process converts methanol to gasoline (MTG) using ZSM-5 zeolite catalysts. In the MTG process, methanol is first dehydrated to dimethyl ether. The methanol and/or dimethyl ether are then converted in a series of reactions that results in formation of a hydrocarbon mixture that comprises aromatic, paraffinie, and olefinic compounds. This mixture may be separated into a liquefied petroleum gas (LPG) fraction and a high-quality gasoline fraction comprising aromatics, paraffins, and olefins. The typical MTG hydrocarbon product consists of about 10-20% olefins and about 40-50% paraffins and 40-50% aromatics, e.g., xylenes, benzene, toluene, etc.

[Θ003] U.S. Patent Nos. 6,423,879 and 6,504,072 disclose processes for the selective production of para-xylene which comprises reacting toluene with methanol in the presence of a catalyst comprising a porous crystalline material having a Diffusion Parameter for 2,2 dimethyl butane of about 0.1-15 sec ^{" 1} when measured at a temperature of 120°C and a 2,2 dimethylbutane pressure of 60 torr (8 kPa). The porous crystalline material is preferably a medium-pore zeolite, particularly ZSM-5, which has been severely steamed at a temperature of > 950°C and which has been combined with about 0.05 to about 20 wt% of at least one oxide modifier, preferably an oxide of phosphorus, to control reduction of the micropore volume of the material during the steaming step. The porous crystalline material is normally combined with a binder or matrix material, preferably silica or a kaolin clay.

[Θ004] U.S. Patent No. 7,304,194 discloses a process for the hydrothermal treatment of a phosphorus-modified ZSM-5 catalyst. In the process, ZSM-5 having a silica/alumina mole ratio of > about 250 and a phosphorus content of from > about 0.08 g P/g zeolite to about 0.15 g P/g zeolite is calcined at a temperature of > 300°C and then contacted with steam at a temperature of from about 150°C to about 250°C. The steamed, phosphorus modified zeolite is said to exhibit improved para-selectivity and methanol selectivity when used as a catalyst in toluene methylation reactions. The steamed, phosphorus modified zeolite may be used as a catalyst in unbound form or in combination with a binder material, such as alumina, clay, and silica.

[Θ005] In addition, U.S. Patent No. 7,285,511 discloses a process of modifying a zeolite catalyst to increase its para-xylene selectivity in toluene methylation reactions, wherein the method comprises forming a slurry consisting essentially of a binder-free ZSM-5-type zeolite having a S1O ₂ /AI2O3 mole ratio of from about 250 to about 1000 and an aqueous solution of a phosphorus-containing compound; and removing water from the slurry to provide a non-steamed, phosphorus treated ZSM-5 zeolite having a phosphorus content of from 0.04 g P/g zeolite or more and a pore volume of from 0.2 mVg or less. The resultant phosphorus treated ZSM-5 can be used as a toluene methylation catalyst either in unbound form or may be composited with a binder, such as alumina, clay, or silica.

[0006] Phosphorus modification is a kno wn method of improving the performance of zeolite catalysts for a variety of chemical processes including, for example, the conversion of methanol to hydrocarbons and the methylation of toluene to produce xylenes. For example, U.S. Patent Nos. 4,590,321 and 4,665,251 disclose a process for producing aromatic hydrocarbons by contacting one or more non-aromatic compounds, such as propane, propylene, or methanol, with a catalyst containing a zeolite, such as ZSM-5, together with a binder or matrix material resistant to the temperature and other conditions employed in the process. The zeolite is modified with phosphorus oxide by impregnating the zeolite with a source of phosphate ions, such as an aqueous solution of an ammonium phosphate, followed by calcination. The phosphorus oxide modification is said to render the zeolite more active and/or benzene selective in the aromatization reaction.

[Θ007] Nevertheless, there is still a need for catalyst compositions having improved selectivity and/or resistance to deactivation and/or persistence in the selectivity of aromatic selectivity.

SUMMARY OF THE INVENTION

[0008] It has been found that one or more of the above needs may be provided by zeolite-containing catalyst compositions enhanced by the presence of a Group 10-12 and a Group 15 element. Such catalysts typically have a high selectivity for desirable aromatic molecules while providing improved catalyst lifetime.

[ΘΘ09] Thus, in one aspect, embodiments of the invention provide a catalyst composition comprising: a zeolite having a molar ratio of silicon to aluminum of about 10.0 to about 300.0; a Group 10-12 element and combinations thereof; a Group 15 element and combinations thereof; and optional ly, a binder, wherein the catalyst composition has a molar ratio of Group 15 element to Group 10-12 element of about 0.01 to about 10.0.

[ΘΘ10] In another aspect, embodiments of the invention provide a catalyst composition comprising an alurmnosiiicate zeolite, zinc, phosphorus, and optionally a binder; the zeolite having a molar ratio of silicon to aluminum of about 10.0 to about 300.0, the catalyst composition comprising 0 to about 80.0 wt% binder, based on a total weight of the catalyst composition and having a micropore surface area of > about 100 m7g, a molar ratio of zinc to aluminum of about 0.1 to about 1 ,3, a molar ratio of phosphorus to zinc of 0.01 to 10.0 and at least one of: (a) a mesoporous surface area of about 20.0 to about 500.0 m ² /g; and (b) a diffusivity for 2,2-dimethylbutane of 1.25 x 10 ^{_ '} to 3.00 x 1 Q ^~2 sec ^"1 , when measured at a temperature of about 120°C and a

2,2-dimethylbutane pressure of about 60 torr (about 8 kPa).

[Θ011] In still another aspect, embodiments of the invention provide a method for organic compound conversion, comprising exposing a first mixture comprising > 10.0 wt% of at l east one oxygenate, based on the weight of the first mixture, to a catalyst composition comprising: an alummosilicate zeolite, zinc, phosphorus, and optionally a binder; the zeolite having a molar ratio of silicon to aluminum of about 10.0 to about 300.0, 0 to about 80.0 wt% binder, based on a total weight of the catalyst composition and having a micropore surface area of > about 100 m ² /g, a molar ratio of zinc to aluminum of about 0.1 to about 1.3, a molar ratio of phosphorus to zinc of 0.01 to 10.0 and at least one of: (a) a mesoporous surface area of about 20 to about 500 m'/g, and (b) a diffusivity for 2,2-dimethylbutane of 1.25 x I0 ^"2 to 3.00 ^χ 10 ^"2 sec ^"1 , when measured at a temperature of about 120°C and a 2,2-dimethylbutane pressure of about 60 torr (about 8 kPa); said exposing being conducted under conditions effective to covert at least a portion of the first mixture into a hydrocarbon containing stream comprising one or more aromatic hydrocarbons, the method being characterized by a deactivation ratio, DR, of < 15 wt% after processing 200.0 to 400 g of oxygenate per gram of the catalyst composition, wherein DR is defined as:

where A _m jiiai is defined as the initial selectivity to aromatics (on a weight % of hydrocarbon product basis) at the beginning of oxygenate processing, and A200-400 is defined as the selectivity to aromatics (on the same basis) after processing 200 to 400 grams of oxygenate per gram of catalyst composition.

[0012 J In sti ll another aspect, embodiments of the invention provide a method for organic compound conversion, comprising providing a first mixture, the first mixture comprising > 10.0 wt% oxygenate based on the wei ght of the first mixture; exposing at a temperature > 300°C and at a pressure > 1 bara a catalyst composition to the first mixture to convert at least a portion of the oxygenate to hydrocarbons, the

hydrocarbons comprising > 50.0 wt% of aromatics, based on the weight of the hydrocarbons, wherein the catalyst composition comprises a zeolite having a molar ratio of silicon to aluminum of 10.0 to 300.0; a Group 12 element selected from the group consisting of Zn, Cd, and combinations thereof; a Group 15 element selected from the group consisting of phosphorus, arsenic, antimony, bismuth, and combinations thereof; and optionally a binder, wherein the catalyst composition has a molar ratio of Group 15 element to Group 12 element of about 0.01 to about 10.0.

BRIEF DESCRIPTION OF THE DRAWINGS

[0Θ13| Figure 1 illustrates the aromatic selectivity of catalyst compositions according to particular embodiments of the invention.

[0014] Figure 2 illustrates the yield of aromatics as a function of methanol processed for catalyst compositions according to particular embodiments of the invention.

[Θ015] Figure 3 illustrates the relative reduction in aromatics yield after steam treatment for catalyst compositions according to particular embodiments of the invention. DETAILED DESCRIPTION

[0016] For the purposes of this invention and the claims thereto, the numbering scheme for the Periodic Table Groups is used as described in Chemical and

Engineering News, 63(5), pg. 27 (1985),

[ΘΘ17] In various aspects, a zeolite catalyst composition is provided, along with methods for use of the catalyst for the conversion of oxygenate feeds to aromatics, olefins, and paraffins with high aromatics yield and/or reduced catalyst deactivation. While some catalyst compositions include a binder, in some cases, the catalyst composition may be referred to as being "self-bound" or "unbound." The terms "unbound" and "self-bound" are intended to be synonymous and mean that such a catalyst composition is free of any inorganic oxide binders, such as alumina or silica, frequently combined with zeolite catalysts to enhance their physical properties.

[0018J The zeolite employed in the present catalyst composition generally comprises at least one medium pore aluminosilicate zeolite or silica alummophosphate (SAPO) having a Constraint index of 1 -12. The Constraint Index may be < about 12.0, < about 1 1.0, < about 10.0, < about 9.0, < about 8.0, < about 7.0, < about 6.0, < about 5.0, < about 4.0, < about 3.0, or < about 2.0. Additionally or alternatively, the Constraint Index may be about > about 1 1.0, > about 10.0, > about 9.0, > about 8.0, > about 7.0, > about 6.0, > about 5.0, > about 4.0, > about 3.0, > about 2.0, or > about 1.0. In any embodiment, the Constraint Index may be 1.0 to about 10.0, 1.0 to about 8.0, 1 to about 6.0, 1 to about 5.0, 1 to about 3.0, 2.0 to about 1 1.0, 3.0 to 10.0, 4.0 to 9.0, or 6.0 to 9.0, etc. Constraint Index is determined as described in U.S. Patent No. 4,016,218, incorporated herein by reference for details of the method.

[0019] Some useful catalysts compositions can include a zeolite having a structure wherein there is at least one 10-member ring channel and no channel of rings having more than 10 members. Some such molecular sieves may be referred to as having a framework type or topology of EUO, PER, IMF, LAU, MEL, MRI, MFS, MTT, MWW, NES, PON, SFG, STF, STI, TUN, or PUN. Particularly useful zeolites can have a BEA, MFI or MEL framework.

[0020] Non-limiting examples of SAPOs useful herein can include one or a combination of SAPO-5, SAPQ-8, SAPO- 1 1, SAPO-16, SAPO-17, SAPO- 18, SAPO-20, SAPO-31 , SAPO-34, SAPO-35, SAPO-36, SAPO-37, SAPO-40, SAPO-41, SAPO-42, SAPO-44, SAPO-47, and SAPO-56.

[0021] Particular other zeolites useful in embodiments of the invention can include ZSM-5, ZSM-1 1 ; ZSM-12; ZSM-22; ZSM-23; ZSM-34, ZSM-35; ZSM-48; ZSM-57; and ZSM-58. Other useful zeolites may include MCM-22, PSH-3, SSZ-25, MCM-36, MCM-49 or MCM-56, with MCM-22, In any embodiment the zeolite may be ZSM-5 or ZSM-1 1. ZSM-5 is described in detail in U.S. Patent Nos. 3,702,886 and RE 29,948. ZSM-11 is described in detail in U.S. Patent No. 3,709,979. ZSM-5 can be particularly useful.

[0022] Generally, a zeolite having the desired activity can have a silicon to alummum molar ratio of about 10.0 to about 300.0. in any embodiment, the molar ratio of silicon to alummum may be < about 300.0, < about 200.0, < about 150.0, < about 125,0, < about 100.0, < about 80,0, < about 60.0, < about 50,0, < about 40.0, < about 30.0, < about 25.0, < about 20.0, < about < 15.0 or about < 10.0. Additionally or alternatively, the molar ratio of silicon to aluminum may be > about 10.0, > about 15,0, > about 20.0, > about 25.0, > about 30.0, > about 40.0, > about 50.0, > about 60.0, > about 80.0, > about 100.0, > about 125.0, > about 150.0, or > about 200.0; e.g., 20.0 to about 200.0, about 30.0 to about 100.0, about 40.0 to about 80.0, about 50.0 to about 50.0, about 15.0 to about 100.0, or about 20.0 to about 40.0.

[0023] Typically, reducing the molar ratio of silicon to aluminum in a zeolite can result in a zeolite with a higher acidity, and therefore in higher activity for cracking of hydrocarbon or hydrocarbonaceons feeds, such as petroleum feeds. However, with respect to conversion of oxygenates to aromatics, such increased cracking activity may not be beneficial, and instead may result in increased formation of residual carbon or coke during the conversion reaction. Such residual carbon can deposit on the zeolite catalyst, leading to deactivation of the catalyst over time. Having a molar ratio of silicon to aluminum of > about 40.0, such as > about 50.0 or > about 60.0, can reduce and/or minimize the amount of additional residual carbon formed due to the acidic or cracking activity of the catalyst.

[0024] It is noted that the molar ratio described herein is a ratio of silicon to aluminum. If a corresponding ratio of silica to alumina is described, the corresponding ratio of silica (Si0 ₂ ) to alumina (AI ₂ O ₃ ) would be twice as large, due to the presence of two aluminum atoms in each alumina stoichiometric unit. Thus, a molar ratio of silicon to aluminum of 10.0 corresponds to a silica to alumina ratio of 20.0.

[ΘΘ25] When used in the present catalyst compositions, the zeolite can be present at least partly in the hydrogen (acid) form. Depending on the conditions used to synthesize the zeolite, this may correspond to converting the zeolite from, for example, the sodium form. This can readily be achieved, for example, by ion exchange to convert the zeolite to the ammonium form followed by calcination in air or an inert atmosphere at a temperature of about 400°C to about 700°C to convert the ammonium form to the active hydrogen form.

[0026] Zeolite catalyst compositions can include and/or be enhanced by a transition metal. Catalyst compositions herein include a Group 10-12 element or combinations thereof, of the Periodic Table. Exemplary Group 10 elements include, nickel, palladium, and/or platinum, particularly nickel. Exemplary Group 1 1 elements include copper, silver, and/or gold, particularly copper. Exemplary Group 12 elements include e.g., zinc and/or cadmium. In particular embodiments, nickel, copper and/or zinc, particularly zinc, may be used. The Group 10-12 element can be incorporated into the zeolite by any convenient method, such as by impregnation or by ion exchange. After impregnation or ion exchange, the Group 10-12 element-enhanced catalyst can be treated in an oxidizing environment (air) or an inert atmosphere at a temperature of about 400°C to about 700°C.

[0027] The amount of Group 10-12 element can be related to the molar amount of aluminum present in the zeolite. Preferably, the molar ratio of the Group 10-12 element to aluminum in the zeolite can be about 0.1 to about 1 ,3. For example, the molar ratio of the Group 10-12 element to aluminum in the zeolite can be about > 0.1, e.g., > about 0.2, > about 0.3, or > about 0.4. Additionally or alternately, the molar ratio of the Group 10-12 element to aluminum in the zeolite can be about < 1.3, such as about < 1.2, < about 1 ,0, or < about 0.8. In any embodiment, the ratio of the Group 10- 12 element to aluminum is about 0.2 to about 1.2, about 0.3 to about 1 .0, or about 0.4 to about 0.8. Still further additionally or alternately, the amount of Group 10-12 element can be expressed as a weight percentage of the self-bound or unbound zeolite, such as having > about 0.1 wt%, > about 0.25 wt%, > about 0.5 wt%, > about 0.75 wt%, or > about 1.0 wt% of Group 10-12 element. Additionally or alternatively, the amount of Group 10-12 element can be present in an amount of < about 20 wt%, such as < about 10 wt%, < about 5 wt%, < about 2.0 wt%, < about 1.5 wt%, < about 1.2 wt%, < about 1.1 wt%, or < about 1.0 wt%. In any embodiment, the amount of Group 10-12 element may be about 0.25 to about 10.0 wt%, about 0.5 to about 5,0 wt%, about 0.75 to about 2.0 wt%, or about 1.0 to about 1.5 wt%, based on the total weight of the catalyst composition excluding the weight of any binder if present.

[0028] Typically, the catalyst compositions herein also include a Group 15 element, e.g., phosphorus, arsenic, antimony, bismuth, and combinations thereof in addition to the transition metal. In any embodiment, the Group 15 element may be phosphorus.

[0029] The Group 15 element can be incorporated into the catalyst composition in any of the same manners described for incorporation of the Group 10-12 element. Any source of convenient source of the Group 1 element may be used, e.g., phosphoric acid (H ₃ PO ₄ ) or ammonium dihydrogen phosphate (NH ₄ H ₂ P0 ₄ ). Typical ly, the catalyst composition has a molar ratio of Group 15 to Group 10-12 element of about 0.1 to about 10.0. In any embodiment, the molar ratio of Group 15 to Group 10-12 element may be < about 10.0, < about 9.0, < about 8.0, < about 7.0, < about 6.0, < about 5.0, < about 4.0, < about 3.0, < about 2.5, < about 1.0, < about 0.5, < about 0.4, < about 0.3, < about 0.2, or < about 0.1. Additionally or alternatively, the molar ratio of Group 15 to Group 10-12 element may be > about 0.1, > about 0.2, > about 0.3, > about 0.4, > about 0.5, > about 1.5, > about 2.0, > about 3.0, > about 4.0, > about 5.0, > about 6.0, > about 7.0, > about 8.0, > about 9.0, or > about 10.0. Ranges of the molar ratio of Group 15 to Group 10-12 element expressly disclosed include combinations of any of the above-enumerated upper and lower limits, e.g., about 0.2 to about 9.0, about 0.4 to about 8.0, about 0,6 to about 6.0, about 0.8 to about 4.0, about 1.0 to about 3.0, about 1.5 to about 2.5, etc. Additionally or alternatively, the amount of Group 15 element can be present in an amount of about < 5.0 wt%, such as < about 2.5 wt%, < about 1 .0 wt%, < about 0.75 wt%, < about 0.50 wt%, < about 0.25 wt%, or < about 0.1 wt%. In any embodiment, the amount of Group 15 element may be about 0.1 to about 5.0.0 wt%, about 0.25 to about 2.0 wt%, about 0.5 to about 1.0 wt%, or about 1.0 wt%, based on the total weight of the catalyst composition excluding the weight of any binder if present. Where the zeolite is a SAPO and the Group 15 element includes phosphorus, the molar amounts and weight percentages of the phosphorus recited in this paragraph shall exclude the amount of phosphorus attributed to the SAPO zeolite.

[Θ030] Additionally or alternatively, the catalyst compositions may also include at least one Group 2 and/or a Group 3 element. As used herein the term "Group 3" is intended to include elements in the Lanthanide series of the Periodic Table. In any embodiment, one or more Group 2 elements (e.g., Be, Mg, Ca, Sr, Ba, and/or Ra) may be used. In other embodiments, one or more Group 3 elements (e.g., Sc and/or Y), a Lanthanide (e.g., La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Trn, Yb, and/or Lu). While an Actinide may be used, such elements are not believed to offer any particular advantage. When present, the total weight of the at least one Group 2 and/or Group 3 elements is from about 0.1 to about 20.0 wt%, based on the total weight of the catalyst composition excluding the weight of any binder if present. In any embodiment, the amount of the at least one Group 2 and/or a Group 3 element may be about 0.25 to about 10.0 wt%, about 0.5 to about 5.0 wt%, about 0.75 to about 2.0 wt%, or about 1.0 to about 1.5 wt%. The presence of Group 2 and/or Group 3 element is believed to reduce coke formation.

[0031] The catalyst composition can employ the zeolite in its original crystalline form or after formulation into catalyst particles, such as by extrusion. A process for producing zeolite extrudates in the absence of a binder is disclosed in, for example, U.S. Patent No. 4,582,815, the entire contents of which are incorporated herein by reference. Preferably, the Group 15 element, the Group 10-12 element, and/or the at least one Group 2 and/or Group 3 element can be incorporated after formulation of the zeolite (such as by extrusion) to form self-bound catalyst particles. Optionally, a self- bound catalyst can be steamed after extnision.

[0032] Thus, embodiments of the catalyst compositions described herein can further be characterized by at least one, at l east two, or al l of the following properties: (a) a mesoporosity (i.e., mesoporous surface area or surface area external to the zeolite) of > about 20.0 m7g, e.g., > about 30.0 m7g, > about 40.0 m ^* Vg, > about 50.0 m/ ^' /g, > about 60.0 m g, > about 70.0 m g, > about 80.0 m7g, > about 90.0 m7g, > about 100.0 m ² /g, or > about 200.0 m7g. Additionally or alternatively, the mesoporous surface area may be < about 500.0 m7g, e.g., < about 400.0 m7 ^' g, < about 300.0 m7 ^' g, < about 200.0 m ² /g, or < about 100.0 m7g. Exemplar}' such ranges for the mesoporous surface are include about 20.0 to 500.0 m /g, about 20.0 to about 400.0 m ² /g, about 20.0 to about 300.0 m ² /g, about 20.0 to about 200.0 m ² /g, about 20.0 to about 100.0 m ² /g, about 20.0 to about 90.0 m7g, about 20.0 to about 80.0 ni ² /g, about 20.0 to about 70.0 m ² /g, about 20.0 to about 60,0 m7g, about 20.0 to about 50.0 ra ² /g, about 30.0 to about 200.0 m ² /g, about 30.0 to about 100.0 m ² /g, about 40.0 to about 100.0 m7g, about 50.0 to about 100.0 ra ² /g, about 60,0 to about 100.0 m7g, about 70.0 to about 100.0 m7g, etc.; (b) a microporous surface area of about 100.0 m ^' /g, e.g., > about 200.0 m ² /g, > about 300.0 m ² /g, > about 340.0 m ² /g, > about 350.0 m ² /g, > about 360.0 m ² /g, or > about 370.0 m7g. Additionally or alternatively, the microporous surface

2 2 2 area may be < about 1000.0 m /g, e.g., < about 750.0 m /g, < about 600.0 m /g, or < about 500.0 mVg. Exemplary such ranges include about 100.0 to about 1000.0 m g, about 200.0 to about 1000.0 m ² /g, about 300 to about 1000.0 m ² /g, about 340.0 to about 1000.0 m'/g, about 350,0 to about 1000.0 m /g, about 360.0 to about 1000.0 m ² /g, about 370.0 to about 1000.0 ni7g, about 100.0 to about 750.0 m ² /g, about 200.0 to about 750.0 m ² /g, about 300.0 to about 750.0 m ^' Vg, about 340.0 to about 750.0 m ² /g, about 350.0 to about 750.0 m ² /g, about 360.0 to about 750.0 m ² /g, about 370.0 to about 750.0 m ² /g, about 360.0 to about 600.0 m /g, or about 350 to about 500,0 m ² /g, etc.; and/or (c) a diffusivity for 2,2-dimethylbutane of > about 1.0 x 10 ^"" sec ^" , e.g., > about 1.10 x 10 ^""2 sec ^"1 , > about 1.15 x 10 ^"2 sec ^"1 , > about 1.20 x 10 ^"2 sec ^{" 1} , > about 1.25 x 10 ^""2 sec ^"1 , or > about 1.50 x 10 ^"2 sec ^" ' Additionally or alternatively, the diffusivity for 2,2- dimethylbutane may be < about 3.00 x 10 ^" ' sec ^"1 , < about 2.75 x 10 ^" " sec ^{" 1} , < about 2.50

-2 - 1 -2 - 1 _? x 10 ^{" '} sec ^" or < about 2.00 x 10 ^{" '} sec ^" . Exemplary such ranges include about 1.0 x 10 ^" ' ^' sec ^"1 to about 3.00 x 10 ^"2 sec ^{" 1} , about 1.25 10 ^"2 to about 3.00 x 10 ^"2 sec ^{" 1} , about 1.50 x

-2 -J

10 ^{" '} to about 2.00 ^x 10 ^"''" sec ^" , etc., when measured at a temperature of about 120°C and a 2,2-dimethylbutane pressure of about 60 torr (about 8 kPa).

[0033] Of these properties, meso porosity and diffusivity for 2,2-dimethylbutane are determined by a number of factors for a gi ven zeolite, including the crystal size of the zeolite. Microporous surface area is determined by the pore size of the zeolite and the availability of the zeolite pores at the surfaces of the catalyst particles. Producing a zeolite catalyst with the desired low (minimum) mesoporosity, microporous surface area, and 2,2-dimethylbutane diffusivity would be well within the expertise of one of ordinary skill in zeolite chemistiy. It is noted that mesopore surface area and micropore surface area can be characterized, for example, using adsorptkm-desorption isotherm techniques within the expertise of one of skill in the art, such as the BET (Brunauer Emmet Teller) method.

[0034J It is noted that the micropore surface area can be characterized for zeolite crystals or a catalyst formed from the zeolite crystals. In various aspects, the micropore surface area of a self-bound catalyst or a catalyst formulated with a separate binder can be > about 100.0 m ² /g, e.g., > about 200.0 m ² /g, > about 300.0 m ² /g, > about 340.0 m7g, > about 350.0 m7g, > about 360.0 m7g, or > about 370.0 m7g. Additionally or alternatively, the microporous surface area may be < about 1000.0 m ^" Vg, e.g., < about 750.0 m7g, < about 600.0 m ² /g, or < about 500.0 m ² /g. Exemplary such ranges include about 100.0 to about 1000.0 m /g, about 200.0 to about 1000.0 m ² /g, about 300 to about 1000.0 m ² /g, about 340.0 to about 1000.0 m ² /g, about 350.0 to about 1000.0 m ² /g, about 360.0 to about 1000,0 m ² /g, about 370.0 to about 1000.0 m ² /g, about 100.0 to about 750.0 m ² /g, about 200.0 to about 750.0 m ² /g, about 300.0 to about 750.0 m ² /g, about 340.0 to about 750.0 m ^' Vg, about 350.0 to about 750.0 m ² /g, about 360.0 to about 750.0 m /g, about 370.0 to about 750.0 m ² /g, about 360.0 to about 600.0 m ² /g, or about 350 to abou t 500.0 m ² /g, etc. Typically, a formul ation of zeoli te crystals into catalyst particles (either self-bound or with a separate binder) can result in some loss of micropore surface area relative to the micropore surface area of the zeolite crystals. Thus, in order to provide a catalyst having the desired micropore surface area, the zeolite crystals can also have a micropore surface area of > about 100.0 m7g, e.g., > about 200.0 m7g, > about 300.0 m7g, > about 340.0 m7g, > about 350.0 m7g, > about 360.0 m7g, or > about 370.0 m7g. Additionally or alternatively, the microporous surface area may be < about 1000.0 m ^' Vg, e.g., < about 750.0 m ^' Vg, < about 600.0 m ^' Vg, or < about 500.0 m7g. Exemplary such ranges include about 100.0 to about 1000.0 mVg, about 200.0 to about 1000.0 mVg, about 300 to about 1000.0 rnVg, about 340.0 to about 1000.0 mVg, about 350.0 to about 1000.0 m ² /g, about 360.0 to about 1000.0 mVg, about 370.0 to about 1000.0 mVg, about 100.0 to about 750.0 mVg, about 200.0 to about 750.0 mVg, about 300.0 to about 750.0 mVg, about 340.0 to about 750.0 mVg, about 350.0 to about 750.0 m ² /g, about 360.0 to about 750.0 mVg, about 370.0 to about 750.0 m g, about 360.0 to about 600.0 m 7g, or about 350 to about 500.0 m7g, etc. As a practical matter, the micropore surface area of a zeolite crystal and/or a corresponding self-bound or bound catalyst as described herein can be < about 1000 m7g, and typically < about 750 m ^" Vg. Additionally or alternately, the micropore surface area of a catalyst (self-bound or with a separate binder) can be < about 105% of the micropore surface area of the zeolite crystals in the catalyst, and typically < about 100% of the micropore surface area of the zeolite crystals in the catalyst, such as from about 80% to about 100% of the micropore surface area of the zeolite crystals in the catalyst. For example, the micropore surface area of a catalyst can be > about 80%> of the micropore surface area of the zeolite crystals in the catalyst, such as > about 85%, > about 90%, > about 95%, > about 97%, or > about 98%, and/or < about 100%), < about 99%. < about 98%, < about 97%, or < about 95%.

[00351 Additionally or alternatively, the diffusivity for 2,2-dimethylbutane of a catalyst composition (self-bound or with a separate binder) can be < about 105.0% of the diffusivity for 2,2-dimethylbutane of the zeolite crystals in the catalyst, and typically < about 100.0%> or of the diffusivity for 2,2-dimethylbutane of the zeolite crystals in the catalyst, such as from about 80.0% to about 100.0% of the diffusivity for 2,2-dimethylbutane of the zeolite crystals in the catalyst. For example, the diffusivity for 2,2-dimethylbutane of a catalyst can be > about 80.0% of the diffusivity for 2,2- dimethylbutane of the zeolite crystals in the catalyst, such as > about 85.0%, > about 90.0%, > about 95.0%, > about 97.0%, or > about 98.0%, and/or < about 100.0%, < about 99.0%», < about 98.0%, < about 97.0%, or < about 95.0%.

[0036] Additionally or alternatively, the catalyst composition comprises particles having a size > about 0.01 μηι, > about 0.05 μιη, > about 0.08 μηι, > about 0.10 μιη, > about 0.20 μιη, or > about 0.50 μηι. Likewise, the catalyst composition may comprise particles wherein the upper limit is < about 0.6 μιτί, < about 0.5 μηι, < about 0.4 μχη, < about 0.3 μηι, < about 0.2 μπι, < about 0.1 μηι, or < about 0.05 μηι. In any

embodiment, the catalyst may comprise particles having a size of about 0.01 μιη to about 0.6 μΐΊΐ, 0.02 to 0.50 μιτι, 0.03 to 0.40 μπι etc. As used herein the term "size" means either the diameter of approximately spherical particles or, where a particle has another shape, the average of the longest dimension and the dimension orthogonal thereto. Particle dimensions and size can be determined by any suitable means, typically microscopically, using a representative number of particles. "Size" may refer to self-bound particles or particles including a binder, or those formed by extrusion of other method.

[Θ037] Additionally or alternatively, catalyst compositions herein may be described by a particle size distribution, D _x , < about 1.0 μηι, < about 0.5 μηι, < about 0.40 \im, < about 0.20 μηι, < about 0.10 μηι, < about 0.05 μηι, or < about 0.01 μηι, where x is 50.0, 90.0, or 95.0. The particle size distribution, , may also be > about 1.0 μηι, > about 0.8 μηι, > about 0.5 μπι, > about 0.20 um, > about 0. 10 μπι, > about 0.05 um, > about 0.01 am . In any embodiment, the particle size distribution, D _x , may be 0.01 to 0.60 μηι, 0.02 to 0.50 um, 0.03 to 0.40 um, 0.01 to 0.05 μηι, 0.10 to 0.60 um, 0.2 to 0.5 μηι, or 0.3 to 0.4 μνα. The particle size distribution, D _x , means that at least x number percent of the particles have a size, as defined above, in the recited range. For example, a catalyst composition described as having a D9 .0 of 0.10 to 0.60 means that at least 90.0 number percent of the particles have a size between 0.10 and 0.60 μ/m. In any embodiment, the particle size may be relatively narrow, i.e., D90.0 or D9 ₅ .0 may be preferred, i.e., a D90.0 or D95.0 of < about 1 μτη, < about 0.5 μχη, or < about 0,4 μιη, 0,01 to 0.60 μιη, 0.02 to 0.50 μιη, 0.03 to 0.40 μιη, 0.01 to 0.05 μιη, 0.10 to 0.60 μιη, 0.2 to 0.5 μηι, or 0.30 to 0.40 μιη,

[ΘΘ38] In some aspects, the catalyst composition can have an alpha value of at least about 10.0, such as at least about 20.0 or at least about 50.0. Additionally or alternatively, the catalyst composition can have an alpha value of < about 1000.0, < about 800.0, < about 700.0, or < about 600.0; e.g., about 10.0 to about 1000.0, about 10.0 to about 800.0, or about 50.0 to 700.0. The alpha value of a catalyst composition is a measure of the acid activity of a zeolite catalyst as compared with a standard silica- alumina catalyst. The alpha test is described in U.S. Patent No. 3,354,078; in the Journal of Catalysis at vol. 4, p. 527 (1965), vol. 6, p. 278 (1966), and vol. 61 , p. 395 (1980), each incorporated herein by reference as to that description. The experimental conditions of the test used herein include a constant temperature of about 538°C and a variable flow ^r rate as described in detail in the journal of Catalysis at vol. 61 , p. 395. The higher alpha values correspond with a more active cracking catalyst.

[0039] As an alternative to forming self-bound catalysts, zeolite crystals can be combined with a binder to form bound catalyst compositions containing a relatively small amount of binder. Suitable binders for zeolite-based catalysts can include various inorganic oxides, such as silica, alumina, zircoma, titania, silica-alumina, cerium oxide, magnesium oxide, or combinations thereof. Generally, a binder can be present in an amount of 0 to about 80.0 wt%. < about 65.0 wt%, < about 40.0 wt%. < about 35.0 wt%, < about 25.0 wt%, or < 20.0 wt%, based on the total weight of the catalyst composition. Additionally or alternatively, the binder may in any embodiment be present in an amount of 0 wt%, > about 1.0 wt%, > about 5.0 wt%, > about 10.0 wt%, or > about 15.0 wt%, e.g., 0 to about 80.0 wt%, about 5.0 to about 40.0 wt%, about 10.0 to about 35.0, about 10.0 to about 25.0, or about 15.0 to about 20.0 wt%. In any embodiment, only a relatively small amount of binder may be present, e.g., an upper limit of about 5.0 wt%, about 2.5 wt%, or about 1.0 wt% and a lower limit of about 0.1 wt%, about 0.5wt% , about 1.0 wt%, such as 0.1 to 5.0 wt%, 0.5 to 2.5 wt%, 0.5 to 1.0 wt ^' %, or 0.1 to 1.0 wt.%. Combining the zeolite and the binder can generally be achieved, for example, by mulling an aqueous mixture of the zeolite and binder and then extruding the mixture into catalyst pellets. A process for producing zeolite extrudates using a silica binder is disclosed in, for example, U.S. Patent No. 4,582,815. Optionally, a bound catalyst can be steamed after extrusion.

[0040] In some aspects, a binder can be used that is substantially free of alumina, such as a binder that is essentially free of alumina. In this description, a binder that is substantially free of alumina is defined as a binder than contains < about 10.0 wt% alumina, such as < about 7.0 wt%, < about 5.0 wt%, or < about 3.0 wt%. A binder that is essentially free of alumina is defined as a binder that contains < about 1.0 wt%, such as about < 0.5 wt%, or < about 0.1 wt%. Additionally or alternately, a binder can be used that contains no intentionally added alumina and/or that contains no alumina within conventional detection limits for determining the composition of the binder and/or the reagents for forming the binder. Although alumina is commonly used as a binder for zeolite catalysts, due in part to ease of formulation of alumina-bound catalysts, in some aspects the presence of alumina in the binder can reduce and/or inhibit the activity of a catalyst composition for converting methanol to aromatics. For example, for a catalyst where the Group 10-12 and/or Group 15 is incorporated into the catalyst after formulation of the bound catalyst (such as by extrusion), the Group 10-12 and/or Group 15 element may have an affinity for exposed alumina surfaces relative to exposed zeolite surfaces, leading to increased initial deposition and/or migration of such elements to regions of the bound catalyst with an alumina surface in favor of regions with a zeolite surface. Additionally or alternately, alumina-bound catalysts can tend to have low micropore surface area, meaning that the amount of available zeolite surface available for receiving a Group 10-12 element and/or Group 15 element may be undesirably low.

[0041 j An example of a suitable binder for forming bound catalysts with a desirable micropore surface area is a silica binder. Optionally but preferably, a suitable binder can be a binder with a surface area of < about 200.0 m7g, e.g., < about 175.0 m ² /g, or < about 150.0 m7g. Without being bound by any particular theory, it is believed that catalysts formed using high surface area binders (such as high surface area alumina binders) can have an increased tendency for deposited added element(s) to migrate to the binder, rather than remaining associated with the zeolite. Unless otherwise specifi ed, the surface area of the binder is defined herein as the combined micropore surface area and mesopore surface area of the binder.

Feedstocks and Products

[0042] In various aspects, catalyst compositions described herein can be used for conversion of oxygen-containing organic compounds (i .e., "oxygenates") in

hydrocarbon feed mixtures to aromatic and/or olefin and paraffin products. In such aspects, catalyst compositions described herein can resist deactivation while maintaining relatively high yield of aromatics. Thus, embodiments of the catalyst compositions described herein can convert, at least a portion of a first mixture comprising an oxygenate to aromatic products.

[Θ043] Likewise, embodiments of the invention provides a method for organic compound conversion, comprising: providing a first mixture comprising > 10.0 wt% oxygenate; and exposing at least a portion of the first mixture to a catalyst composition described herein under conditions effective to convert at least a portion of the oxygenate to a hydrocarbons, the hydrocarbons comprising > 50.0 wt% of aromatics, based on the weight of the hydrocarbons.

[0044] As used herein the phrase "at least a portion of means >0 to 100.0 wt% of the process stream or composition to which the phrase refers. Thus, the phrase "at least a portion of may mean < about 1.0 wt%, < about 2.0 wt%, < about 5.0 wt%, < about 10.0 wt%, < about 20.0 wt%, < about 25.0 wt%, < about 30.0 wt%, < about 40.0 wt%, < about 50.0 wt%, < about 60.0 wt%, < about 70.0 wt%, < about 75.0 wt%, < about 80.0 wt%, < about 90.0 wt%, < about 95.0 wt%, < about 98.0 wt%, < about 99.0 wt%, or 100.0 wt%. Additionally or alternatively, the phrase "at least a portion of can mean

> about 1.0 wt%, > about 2.0 wt%, > about 5.0 wt%, > about 10.0 wt%, > about 20.0 wt%, > about 25.0 wt%, > about 30.0 wt%, > about 40.0 wt%, > about 50.0 wt%, > about 60.0 wt%, > about 70.0 wt%, > about 75.0 wt%, > about 80.0 wt%, > about 90.0 wt%, > about 95.0 wt%, > about 98.0 wt%, > about 99.0 wt%. Ranges expressly disclosed include combinations of any of the above-enumerated values, e.g., about 10.0 to 100.0 wt%, about 10.0 to about 98.0 wt%, about 2.0 to about 10.0 wt%, about 40.0 to about 60.0 vvt%, etc.

[0045] As used herein the term "first mixture" means a hydrocarbon-containing composition including one or more oxygenates. Typically, the first mixture comprises

> 10.0 wt% of at least one oxygenate, based on the weight of the first mixture. In any embodiment, the amount of oxygenate(s) in the first mixture may be < about 10.0 wt%,

< about 12,5 wt%, < about 15.0 wt%, < about 20.0 wt%, < about 25.0 wt%, < about 30.0 wt%, < about 35.0 wt%, < about 40.0 wt%, < about 45.0 wt%, < about 50.0 wt%,

< about 55.0 wt%, < about 60.0 wt%, < about 65.0 wt%, < about 70.0 wt%, < about 75.0 wt%, < about 80.0 wt%, < about 85.0 wt%, < about 90.0 wt%, < about 95.0 wt%,

< about 99.0 wt%, < about 99.5 wt%, or 100.0 wt%. Additionally or alternatively, the amount of oxygenate in the first mixture may be > about 10.0 wt%, > about 12.5 wt%,

> about 15.0 wt%, > about 20.0 wt%, > about 25.0 wt%, > about 30.0 wt%, > about 35.0 wt%, > about 40.0 wt%, > about 45.0 wt%, > about 50.0 wt%, > about 55.0 wt%,

> about 60.0 wt%, > about 65.0 wt%, > about 70.0 wt%, 75.0 wt%, > about 80.0 wt%,

> about 85.0 wt%, > about 90.0 wt%, > about 95.0 wt%, > about 99.0 wt%, > about 99.5 wt%, or 100.0 wt%. Ranges expressly disclosed include combinations of any of the above-enumerated upper and lower limits, e.g., 10.0 to 100.0 wt%, 12.5 to 99.5 wt%, 20.0 to 90.0, 50.0 to 99.0 wt%, etc.

[0046] As used herein the tenn "oxygenate" refers to oxygen-containing compounds having 1 to about 50 carbon atoms, 1 to about 20 carbon atoms, 1 to about 10 carbon atoms, or 1 to about 4 carbon atoms. Exemplary oxygenates can include alcohols, ethers, carbonyl compounds, e.g., aldehydes, ketones and carboxylic acids, and mixtures thereof. Particular oxygenates can include one or a combination of methanol, ethanol, dimethyl ether, diethyl ether, methylethyl ether, di-isopropyl ether, dimethyl carbonate, dimethyl ketone, formaldehyde, and acetic acid.

[Θ047] In any embodiment, the oxygenate comprises one or more alcohols, preferably alcohols having 1 to about 20 carbon atoms, 1 to about 10 carbon atoms, or I to about 4 carbon atoms. The alcohols useful as first mixtures may linear or branched, substituted or unsubstituted aliphatic alcohols and their unsaturated counterparts. Non- limiting examples of such alcohols include methanol, ethanol, propanols (e.g., n- propanol, isopropanol), butanols (e.g., n-butanol, sec-butanol, tert-butyl alcohol), pentanois, hexanols, etc and mixtures thereof. In any embodiment described herein, the first mixture may comprise or be one or more of methanol, and/or ethanol, particularly methanol. In any embodiment, the first mixture may be methanol and dimethyl ether.

[0048] The oxygenate, particularly where the oxygenate comprises an alcohol (e.g., methanol), may optionally be subjected to dehydration, e.g., catalytic dehydration over e.g., γ-a!umina. Typically, such catalytic dehydration decreases the amount of water in the oxygenate by converting a portion of the water and alcohol to an ether, e.g., dimethyl ether (DME) in the first mixture. Further optionally, at least a portion of any methanol and/or water remaining in the first mixture after catalytic dehydration may be separated from the first mixture.

[0049] In any embodiment, one or more other compounds may be present in first mixture. Some common or useful such compounds have 1 to about 50 carbon atoms, 1 to about 20 carbon atoms, 1 to about 10 carbon atoms, or 1 to about 4 carbon atoms. Typically, although not necessarily, such compounds can include one or more heteroatoms other than oxygen Some such compounds can include amines, halides, mercaptans, sulfides, or the like, or a combination thereof. Particular such compounds can include alky] -mercaptans (e.g., methyl mercaptan and ethyl mercaptan), alkyl- sulfides (e.g., methyl sulfide), alkyl-ammes (e.g., methyl amine), alkyl-halides (e.g., methyl chloride and ethyl chloride), or a combination thereof. In any embodiment, the amount of such other compounds in the first mixture may be < about 2.0 wt%, < about 5.0 wt%, < about 10.0 wt%, < about 15.0 wt%, < about 20.0 wt%, < about 25.0 wt%, < about 30.0 wt%, < about 35.0 wt%, < about 40.0 wt%, < about 45.0 wt%, < about 50.0 wt%, < about 60.0 wt%, < about 75.0 wt%, < about 90.0 wt%, or < about 95.0 wt%. Additionally or alternatively, the amount of such other compounds in the first mixture may be > about 2.0 wt%, > about 5.0 w†%, > about 10.0 wt%, > about 15.0 w†%, > about 20.0 wt%, > about 25.0 wt%, > about 30.0 wt%, > about 35.0 wt%, > about 40.0 wt%, > about 45.0 wt%, > about 50.0 wt%, > about 60.0 wt%, > about 75.0 wt%, or > about 90.0 wt%. Ranges expressly disclosed include combinations of any of the above- enumerated upper and lower limits, e.g., 1.0 to 10.0 wt%, 2.0 to 5.0 wt%, 10.0 to 95.0 wt%, wt%, 15.0 to 90.0 wt%, 20.0 to 75.0 wt%, 25.0 to 60 wt%, 30.0 to 50 wt%, 35.0 to 45 wt%, about 40.0 wt%, etc. The oxygenate feed can be derived from any convenient source. For example, the oxygenate feed can be formed by reforming of hydrocarbons in a natural gas feed to form synthesis gas (¾, CO, CO?), and then using the synthesis gas to form alcohols.

[0050] In various aspects, the yield of aromatics relative to the total hydrocarbon product can be at least about 53.0 w†%, such as > about 55.0 wt%, > about 57.0 wt%, or > about 59,0 wt%. In some aspects, the total C5+ (liquid) product yield can be greater than the yield of aromatics by < about 10.0 wt%, such as greater than the yield of aromatics by < about 8.0 wt% or by < about 6.0 wt%. For example, in an aspect where the yield of aromatics relative to the total hydrocarbon product is about 60.0 wt%, the yield of total liquid product can be about 65.0 wt%. In some aspects, the combined yield of aromatics and olefins in the total hydrocarbon product can be > about 70.0 wt%, such as > about 75.0 wt% or > about 80.0 wt%. It is noted that olefins in the hydrocarbon product can include (gaseous) C ₂ -C ₄ olefins, and therefore the amount of aromatics plus olefins in the total hydrocarbon product may not necessarily directly relate to the C ₅₊ (liquid) yield in the total hydrocarbon product.

[ΘΘ51] In some aspects, converting oxygenates to aromatics and/or olefins in the presence of a catalyst composition as described herein can be beneficial for producing a mixture of aromatics with a desirable composition. For example, in some aspects, converting oxygenates to aromatics as described herein can result in production of aromatics with an increased percentage of Co and C ₁₀ aromatics relative to the total aromatics produced. In additional or alternate aspects, production of C ₆ and C ₇ aromatics can be enhanced.

[0052] In some aspects, converting an oxygenate feed to aromatics in the presence of a catalyst composition as described herein can reduce and/or minimize the amount of coke formation, that occurs during conversion. [0053] Suitable and/or effective conditions for exposing the first mixture to a catalyst composition can include temperatures > 300.0°C, e.g., > about 375.0°C, such as > about 400.0°C, > about 450.0°C, > 460.0°C. Additionally or alternately, the temperature can be < about 550.0°C, < about 525.0°C, or < about 500.0°C. Effective pressures include those wherein the total pressure is > 1.0 bara, e.g., from 1.0 to about 35 bara. Any suitable oxygenate space velocity may be used. Oxygenate space velocities between about 0.1 h ^"3 to about 20 h ^~ \ based on weight of oxygenate relative to weight of cataiyst, are typical. In any embodiment, the methods herein can include exposing at least a portion of the first mixture to the catalyst composition at a temperature > 300°C and a pressure of 1.0 to about 35 bara, at an oxygenate space velocity of about 0.1 h ^~l to about 20 h ^~ \

[0054] It is noted that the oxygenate feed and/or conversion reaction environment can include water in various proportions. Conversion of oxygenates to aromatics and olefins can result in production of water as a product, so the relative amounts of oxygenate (such as methanol or dimethyl ether) and water can vary within the reaction environment. Based on the temperatures present during methanol conversion, the water in the reaction environment can result in "steaming" of a catalyst. Thus, a catalyst used for conversion of oxygenates to aromatics can advantageously be a catalyst that can substantially retain activity when steamed. Water may additionally or alternately be present in a feed prior to contacting the zeolite catalyst. For example, in commercial processing of methanol to form gasoline, in order to control heat release within a reactor, an initial catalyst stage may be used to convert a portion of the methanol in a feed to dimethyl ether and water prior to contacting a zeolite catalyst for forming gasoline.

[0055] Additionally or alternatively, catalysts and methods described herein can be characterized by a deactivation ratio, DR, after processing an amount of oxygenate per gram of the catalyst composition, wherein DR is defined as:

where A; _lut j _a | is defined as the initial selectivity to aromatics (on a weight % of hydrocarbon product basis) at the beginning of oxygenate processing, and A _y is defined as the selectivity to aromatics (on the same basis) after processing "y" grams of oxygenate per gram of catalyst composition. The deactivation ratio, DR, may be < about 25.0%, < about 20.0%, < about 15.0%, < about 12.5%, < about 10.0%, < about 7.5%, < about 5.0%, or < about 2.5%. Additionally or alternatively, the deactivation ratio, DR, may be > about 12.5%, > about 10.0%), > about 7.5%, > about 5.0%, > about 2.5%, or > about 1.0%. Ranges of the deactivation ratio, DR, expressly disclosed include combinations of any of the abov e-enumerated upper and lower limits, e.g., about 1.0%) to about 15.0%, about 2.5 to about 12.5%, about 5.0 to about 10.0%, etc. The deactivation ratio, DR, may be determined after any value of A _y between 200.0 and 400.0, such as 200.0, 250.0, 300.0, 350.0, or 400.0. Combinations of DR and A _y having these upper and lower limits are expressly disclosed, e.g. DR may be 1.0% to about 15.0%, about 2.5 to about 12.5%, about 5.0 to about 10.0%, etc at a A _y of 200.0, 250.0, 300.0, 350.0, or 400.0, such as DR may be < about 25.0%, < about 20.0% , < about 1 .0%, or < about 10.0% when y = 400.0, DR may be < about 20%, < about 15.0%) , < about 10.0%, or < about 5.0% when y = 300.0DR may be < about 20%, < about 15.0% , < about 10.0%, or < about 5.0% when y = 200.0. Alternatively, DR may be in the range of about 5.0 to about 25.0%, about 5.0 to about 20.0%, about 5.0 to about 15.0, or about 10.0 to about 25.0% when y is 200.0, 300.0, or 400.0.

[0056] Additionally or alternatively, embodiments of the invention may be characterized by a resilience of aromatic production after steam treatment at about 540°C for 24 hours. Resilience refers to the relative amount of aromatics produced by a catalyst composition comprising both a Group 10-12 element and a Group 15 element compared to that produced by a fresh, unsteamed zeolite catalyst composition comprising neither a Group 10-12 nor a Group 15 element. The relative amount of aromatics produced may be < about 0,55, < about 0.50, < about 0,45, < about 0.40, < about 0,30, < about 0.25, or < about 0.20. Additionally or alternatively, the relative amount of aromatics produced may be < about 0.55, < about 0,50, < about 0.45, < about 0.40, < about 0.30, < about 0.25, or < about 0.20. Ranges of the relative amount of aromatics having these upper and lower limits are expressly disclosed, e.g., about 0.20 to about 0.55, about 0.25 to about 0.50, about 0.30 to about 0.45, about 0.25 to about 0.35, etc. Additional embodiments

[0057] Embodiment 1 : A catalyst composition comprising: a zeolite having a molar ratio of silicon to aluminum of about 10.0 to about 300.0; a Group 10-12 element and combinations thereof; a Group 15 element and combinations thereof; and optionally, a binder, wherein the catalyst composition has a molar ratio of Group 15 element to Group 10-12 element of about 0.01 to about 10.0.

[0058] Embodiment 2: A catalyst composition comprising a silicoaluminate zeolite, zinc, phosphorus, and optionally a binder; the zeolite having a molar ratio of silicon to aiumimim of about 10.0 to about 300.0, the catalyst composition comprising 0 to about 80.0 wt% binder, based on a total weight of the catalyst composition and having a microporo s surface area of > about 100.0 m 7g, a molar ratio of zinc to aluminum of about 0.1 to about 1.3, a molar ratio of phosphorus to zinc of 0.01 to 10.0 and at least one of: a) a mesoporous surface area of > about 20.0 m ^' V ^' g, about 20.0 to 500. m /g, 20.0 to 200.0 or about 30.0 to 100.0 m ² /g; and b) a diffusivity for 2,2-dimethylbutane of > about 1 10 ^"2 sec ^"1 , 1 .25 ^χ 10 ^"2 to 3.00 10 ^"' sec ^"1 , or 1.50 >· 10 ^"2 to 2.00 ^χ 10 ^"2 sec ^"1 , when measured at a temperature of about 120°C and a 2,2-dimethylbutane pressure of about 60 torr (about 8 kPa).

[0059] Embodiment 3: The catalyst according to any of Embodiments 1-2, wherein the catalyst composition has a molar ratio of Group 15 element (e.g., phosphorus) to Group 12 element (e.g., zinc) of about 0.2 to about 9.0, about 0.4 to about 8.0, about 0.6 to about 6.0, about 0.8 to about 4.0, about 1.0 to about 3.0, or about 1.5 to about 2.5.

[0060] Embodiment 4. The catalyst according to any of Embodiments 1-3, having a Group 12 element (e.g., zinc) to aluminum molar ratio of 0.1 to 1.3, about 0.2 to about 1.2, about 0.3 to about 1 .0,or about 0.4 to about 0.8.

[Θ061] Embodiment 5: The catalyst according to any of Embodiments 1-4, wherein the Group 10-12 element is selected from the group consisting of Zn, Cd, and combinations thereof (is zinc).

[0062] Embodiment 6. The catalyst according to any of Embodiments 1-5, wherein the zeolite has a molar ratio of silicon to aluminum of about 20.0 to about 200.0, about 30.0 to about 100.0, about 40.0 to about 80.0, about 15.0 to about 100.0 or 20.0 to about 40.0. [0063] Embodiment 7: The catalyst according to any of Embodiments 1 ~6, wherein the Group 10-12 element (e.g., zinc) is present in an amount of about 0.1 to about 20.0 wt%, about 0.25 to about 10.0 wt%, about 0.5 to about 5.0 wt%, about 0.75 to about 2.0 wt%, or about 1.0 to about 1 .5 wt%, based on the total weight of the catalyst composition excluding the weight of any binder if present.

[0064] Embodiment 8: The catalyst according to any of Embodiments 1 -7, wherein the catalyst composition further comprises at least one Group 2 and/or a Group 3 element, preferably wherein the total weight of the at least one Group 2 and/or Group 3 elements is from about 0.1 to about 20.0 wt%, about 0.25 to about 10.0 wt%, about 0.5 to about 5.0 wt%, about 0.75 to about 2.0 wt%, or about 1.0 to about 1.5 wt%, based on the total weight of th e catalyst composition excluding the weight of any binder i f present.

[0065J Embodiment 9: The catalyst according to any of Embodiments 1-8, wherein the catalyst composition comprises < about 80.0 wt%, about 1.0 to about 80.0 wt%, about 5.0 to about 40 wt%, 10.0 to about 35.0 wt%, 10.0 to about 25.0, or about 15.0 to about 20.0 wt%, of the binder, based on a total weight of the catalyst composition.

[0066] Embodiment 10: The catalyst according to any of Embodiments 1-9, wherein the catalyst composition has a microporous surface area > 100.0 m /g, > 200.0 m ² /g, > 300.0 m ² /g, > about 340.0 m ² /g, about 340.0 to 1000.0 m ² /g, about 350.0 to about 750.0 mVg, about 360.0 to about 600.0 m7g, or about 350.0 to about 500.0 m7g.

[0067] Embodiment 1 1 : The catalyst according to any of Embodiments 1-10, wherein the catalyst composition has at least one of the following: (a) a mesoporous surface area of > about 20 m ² /g, about 20 to 500 m /g, about 20.0 to 200 m7g, or about 30 to 100 m7g; and (b) a diffusivity for 2,2-dimethylbutane of > about 1 x 10 ^~2 sec ^"1 , 1.25 10 ^"2 to 3.00 10 ^"2 sec ^"1 , or 1.50 10 ^"2 to 2.00 ^χ 10 ^"2 sec ^"1 , when measured at a temperature of about 120°C and a 2,2-dimethylbutane pressure of about 60 torr (about 8 kPa).

[0068] Embodiment 12: The catalyst according to any of Embodiments 1-11, wherein the catalyst composition has an alpha value of > about 10.0, about 10.0 to about 1000.0, about 10.0 to about 800.0, or about 50.0 to about 700.0.

[0069] Embodiment 13: The catalyst according to any of Embodiments 1-12, wherein the catalyst composition comprises a binder having a surface area of < about 500.0 m ² /g, about 400.0 m ² /g, <about 200.0 m ² /g, about 50.0 to about 200.0 rn u. about 75.0 to about 175.0 m7g, or about 100.0 to about 150.0 m7g.

[Θ070] Embodiment 14: The catalyst according to any of Embodiments 1-13, wherein the cataly st composi tion compri ses a binder, and wherein one or more of the following is satisfied: the binder is at least one of substantially free of alumina (i.e., contains about < 10.0 wt% alumina, < about 7.0 wt%, < about 5.0 wt%, or < about 3.0 wt% alumina) and essentially free of alumina (i.e., contains about < 1.0 wt%, such as about < 0.5 wt%, or < about 0.1 wt% alumina); and the binder comprises silica, fitania, zirconia, cerium oxide, magnesium oxide, or a combination thereof (e.g., is silica).

[0071] Embodiment 15: The catalyst according to any of Embodiments 1-14, wherein the catalyst composition comprises from 0 to about 70.0 wt%, particularly, about 5.0 wt% to about 40.0 wt%, binder, based on the total weight of the catalyst composition, and additionally or alternatively has a mesoporosity of about 20 to 500 m ² /g.

[0072] Embodiment 16: The catalyst according to any of Embodiments 1-15, wherein the catalyst composition has a diffusivity for 2,2-dimethylbutane of 1.25 10 ^"* to 3.00 Hi ^'" .sec \ or 1 .50 10 ^""2 to 2.00 Hi \ec \

[Θ073] Embodiment 17: The catalyst according to any of Embodiments 1-16, wherein the zeolite satisfies one or more of the following: the zeolite has a constraint index of about 1 to about 12; the zeolite comprises a zeolite having an MFI framework, a zeolite having an MEL framework, a zeolite having a BEA framework, or a combination thereof; the zeolite comprises or is ZSM-5; the zeolite comprises or is ZSM-i l .

[0074] Embodiment 18: The catalyst according to any of Embodiments 1 -17, wherein the catalyst composition has both a) a mesoporous surface area of > about 20.0 m7g, about 20.0 to 500 m7g, about 20.0 to about 200.0 nr/g, or about 30 to 100 m7g; and b) a diffusivity for 2,2-dimethylbutane of > about 1 x 10 ^"2 sec ^"1 , 1.25 x 10 ^"2 to 3.00 x lO ^{" '} sec ^"1 , or 1.50 ^x 10 ^~2 to 2.00 ^x 10 ^" ' sec ^"1 , when measured at a temperature of about 120°C and a 2,2-dimethylbutane pressure of about 60 torr (about 8 kPa).

[Θ075] Embodiment 19: The catalyst according to any of Embodiments 1-18, wherein the catalyst composition comprises particles having a size of about 0.01 am to about 0.6 μτη and/or a DQ ₀ particle size distribution of < about 1 μπΐ, < about 0.5 μτη, or < about 0.4 μη .

[Θ076] Embodiment 20: A method for organic compound conversion, comprising: providing a first mixture, the first mixture comprising > 10.0 wt% oxygenate based on the weight of the first mixture; exposing at a temperature > 300°C at a pressure > 1 bara a catalyst composition of any of Embodiments 1-19 to the first mixture to convert at least a portion of the oxygenate to a hydrocarbons, the hydrocarbons comprising > 50.0 wt% of arom.ati.es, based on the weight of the h ydrocarbons.

[0077] Embodiment 21 : A method for organic compound conversion, comprising exposing the catalyst composition of any of Embodiments 1-19 to a first mixture comprising > 10.0 wt% of at least one oxygenate, based on the weight of the first mixture; said exposing being conducted under conditions effective to covert at least a portion of the first mixture into a hydrocarbon containing stream comprising one or more aromatic hydrocarbons.

[0078] Embodiment 22: A method for organic compound conversion, comprising exposing the catalyst composition of any of Embodiments 1-19 to a first mixture comprising > 10.0 wt% of at least one oxygenate, based on the weight of the first mixture; said exposing being conducted under conditions effective to covert at least a portion of the first mixture into a hydrocarbon containing stream comprising one or more aromatic hydrocarbons wherein the hydrocarbon stream comprises > 50.0 wt% aromatic hydrocarbons.

[0079] Embodiment 23: A method for organic compound conversion, comprising exposing the catalyst composition of any of Embodiments 1-19 to a first mixture comprising > 10.0 wt% of at least one oxygenate, based on the wei ght of the first mixture; said exposing being conducted under conditions effective to covert at least a portion of the first mixture into a hydrocarbon containing stream comprising one or more aromatic hydrocarbons, the method is characterized by a deactivation ratio , DR, of < 15 wt% after processing 200.0 to 400 g of oxygenate per gram of the catalyst composition, wherein DR is defined as: where Α _ί „ _¾α1 is defined as the initial selectivity to aromatics (on a weight % of hydrocarbon product basis) at the beginning of oxygenate processing, and A?oo-40o is defined as the selectivity to aromatics (on the same basis) after processing 200 to 400 grams of oxygenate per gram of catalyst composition.

Experimental

[0080] The following examples show data from testing and analysis of a variety of ZSM-5-based self-bound catalyst compositions for performing a methanol to aromatics reaction. After forming ZSM-5 with a desired micropore surface area, the catalysts are formed into self-bound catalyst particles using a procedure similar to the following. It is noted that the absolute values in grams provided below should be considered as representative of using an appropri ate ratio of the various components.

[0081] ZSM-5 crystal (about 1,400 grams on a solids basis) was added to a mixer and dry mulled. Then, approximately 190 grams of deionized water w ^r as added during mulling. After about 10 minutes, about 28 grams of about 50 wt% caustic solution mixed with about 450 grams of deionized water were added to the mixture and mul led for an additional 5 minutes. The mixture was then extruded as formed catalyst pellets. The extrudates were dried overnight at about 250°F (about ! 21°C) and then calcined in nitrogen for about 3 hours at about 1000°F (about 538°C). The extrudates were then contacted with a I N solution of ammonium nitrate, twice. The exchanged extrudates were dried overnight at about 250°F (about 121°C) and then calcined in air for about 3 hours at about 1000°F (about 538°C).

[Θ082] In the following examples, some of the ZSM-5-based catalyst compositions included a Group 12 element, such as Zn or Cd, and a Group 15 element, particularly phosphorus. To form the catalysts compositions described below, a self-bound catalyst as described above was impregnated via incipient wetness with a solution containing the desired Group 12 and Group 15 elements for impregnation. The impregnated crystal was then dried overnight at about 250°F (about 121°C) and then calcined in air for about 3 hours at about 1000°F (about 538°C).

[0083] In the discussion below, references to the micropore surface area of a catalyst composition correspond to the micropore surface area of the self-bound catalyst. The procedure for self-binding may cause some reduction in micropore surface area of the catalyst composition rel ative to the micropore surface area of the corresponding zeolite crystals prior to self-binding.

Example 1 - Catalyst Composition versus Aromatics Yield

[0084J The aromatics yield during methanol conversion of five exemplary ZSM-5 based catalyst compositions (an H-ZSM-5 catalyst, a 1 wt% Zn/H- ZSM-5 catalyst, and three Zn/P/H-ZSM-5 catalysts with various P/Zn ratios (1 wt% Zn in all cases) are shown in Table 1. The aromatic content (wt% of hydrocarbon product) during methanol conversion at about 500°C, an inlet feed pressure of about 15 psig (about 1 10 kPag), about 20 WHSV(g-CH ₃ OH g-catalyst ^"1 h ^! ;·. and 100% Cf hO! l conversion is also shown graphically in Figure 1. The inlet feed was a mixture of methanol and water, to provide about 13.5 psig (about 95 kPag) of CH ₃ OH and about 1.5 psig (about 1 1 kPag) of H ₂ 0. Unless otherwise indicated, the methanol conversion reactions were performed in a tubular stainless steel reactor. Note that in Table 1 (as well as tables in the other Examples), the ZSM-5 is described in terms of a ratio of Si to Al ₂ . The corresponding molar ratio of silicon to aluminum is half of the value of the Si to AI ₂ ratio,

[0085] For the catalysts in Table 1 , all of the catalysts corresponded to self-bound catalysts. As shown in Table 1, the relative increase in aromatic yields afforded by Zn addition to H-ZSM-5 was maintained when P was added to the Zn/H-ZSM-5 catalyst. However, aromatic yields appeared to decrease above a phosphorus loading of about 1 wt ^' %.

Table 1 -Aromatics Yield as a Function of Catalyst Composition

Catalyst Aromatics (wt%) in

Zn Content P Content

Composition Zeolite Si/A! ₂ hydrocarbon

(wt%) (wt%)

product la H-ZSM-5 -60 0 0 -30 lb H-ZSM-5 -60 1.0 0 -58 lc H-ZSM-5 -60 1.0 0.3 -58

Id H-ZSM-5 -60 1.0 0.6 -57 le H-ZSM-5 -60 1.0 0.9 -55 Example 2 - Aromatics Yield versus Amount of Methanol Processed

[0086] In this example, the aromatics yiel d versus the amount of methanol processed for three exemplary ZSM-5 -based catalyst compositions (an H-ZSM-5 catalyst, a 1 wt% Zn/e- ZSM-5 catalyst, and a l .wt% Zn/1.4 wt% P/H-ZSM-5 catalyst) was determined under substantially the same reaction conditions as in Example 1. Results are tabulated in Table 2, As shown in Figure 2, the P-containing Zn/H-ZSM-5 catalyst appeared to maintain the highest (45-50%) yield of aromatics with increasing methanol processed (time on stream), whereas the aromatic yields for the H-ZSM-5 and Zn I H-ZSM-5 catalysts appeared to decrease considerably.

Table 2 - Aromatics Yield versus Amount of Methanol Processed

Example 3 -- Effect of Steaming on Aromatic Selectivity

[ΘΘ87] In this example, the catalyst compositions lb, lc, and le of Example 1 were steam treated at about 540°C for 24 hours to simulate an aged catalyst that had undergone severe steam deactivation. Results are reported in Table 3 and illustrated graphically in Figure 3. These results showed the relative percent reduction in aromatic yields during methanol conversion for the steamed catalyst compositions compared to the fresh, unsteamed Zn/H-ZSM-5 catalyst (i.e., catalyst composition la). The relative reduction in aromatic yield for catalyst compositions lc (0.3 wt% P) and le (0.9 wt% P) after steaming appeared to be less than that of the fresh, unsteamed catalyst composition la, suggesting that the long term stability of Zn/H-ZSM-5 for aromatic production from methanol may be improved by the addition of phosphorus to the catalyst composition. Table 3 - Relative Aroma tics Yield After Sieam Treatment

[0088] All documents described herein are incorporated by reference herein for purposes of all jurisdictions where such practice is allowed, including any priority documents and/or testing procedures to the extent they are not inconsistent with this text, provided however that any priority document not named in the initially filed application or filing documents is NOT incorporated by reference herein. As is apparent from the foregoing general description and the specific embodiments, while forms of the invention have been illustrated and described, various modifications can be made without departing from the spirit and scope of the invention. Accordingly, it is not intended that the invention be limited thereby. Likewise, the term "comprising" is considered synonymous with the term "including" for purposes of Australian law. Likewise whenever a composition, an element or a group of elements is preceded with the transitional phrase "comprising," it is understood that we also contemplate the same composition or group of elements with transitional phrases "consisting essentially of," "consisting of," "selected from the group of consisting of," or "is" preceding the recitation of the composition, element, or elements and vice versa.