US20220314207A9

US20220314207A9 - Catalytic compositions for the oxidation of substrates

Info

Publication number: US20220314207A9
Application number: US17/217,782
Authority: US
Inventors: Yuriy Román-Leshkov; Randall J. Meyer; Pedro M. SERNA MERINO; Mark Sullivan; Kimberly Dinh
Original assignee: Massachusetts Institute of Technology; ExxonMobil Research and Engineering Co
Current assignee: Massachusetts Institute of Technology; ExxonMobil Technology and Engineering Co
Priority date: 2020-03-31
Filing date: 2021-03-30
Publication date: 2022-10-06
Also published as: US20210346875A1

Abstract

Catalytic compositions and sequential catalytic methods are generally described. in some embodiments, a composition comprises a first catalyst comprising a Cu-modified zeolite, and a second catalyst capable of a coupling reaction between (a) an intermediate resulting from a reaction of a reactant at the first catalyst, and (b) a co-reagent, wherein a rate of diffusion of the co-reagent within one or more cages and/or pores of the first catalyst is lower than a rate of diffusion of the intermediate within the one or more cages and/or pores of the first catalyst.

Description

RELATED APPLICATIONS

This application claims priority to U.S. Provisional Patent Application Ser. No. 63/002,415, filed Mar. 31, 2020, entitled “Direct Aromatic Alkylation Using Methane Over Copper-Zeolite Systems,” and U.S. Provisional Patent Application Ser. No. 63/029,751, filed May 26, 2020, entitled “Catalytic Compositions for the Oxidation of Substrates,” both of which are incorporated herein by reference in their entireties for all purposes.

TECHNICAL FIELD

Catalytic compositions and sequential catalytic methods are generally described.

BACKGROUND

The selective oxidation of methane (CH₄) to useful products is a significant challenge in catalysis due to a selectivity-conversion limit stemming from the relative ease of continued oxidation of partially oxidized CH₄-derived products. This selectivity-conversion limit, combined with the global abundance of natural gas reserves, makes selective CH₄oxidation at mild conditions and small scales an attractive alternative to current large-scale two-step industrial processes. The selective activation of CH₄can be obtained at mild conditions, but CH₄conversion is limited (e.g., to ˜0.01%). Selectivity is expected to decrease quickly with increasing CH₄conversion. Therefore, improved compositions and methods related to the oxidation of alkanes (e.g., CH₄) are necessary.

SUMMARY

Catalytic compositions and methods are provided, some of which relate to the oxidation of an alkane. The subject matter of the present invention involves, in some cases, interrelated products, alternative solutions to a particular problem, and/or plurality of different uses of one or more systems and/or articles.
According to certain embodiments, a composition is described, the composition comprising a first catalyst comprising a Cu-modified zeolite, and a second catalyst capable of a coupling reaction between (a) an intermediate resulting from a reaction of a reactant at the first catalyst, and (b) a co-reagent, wherein a rate of diffusion of the co-reagent within the cages and/or pores of the first catalyst is lower than a rate of diffusion of the intermediate within the cages and/or pores of the first catalyst.
In certain embodiments, a composition is described, the composition comprising a first catalyst comprising a Cu-modified zeolite, and a second catalyst capable of a coupling reaction, wherein the coupling reaction is alkylation and/or etherification.
According to some embodiments, a method is described, the method comprising exposing a reactant to a first catalyst comprising a Cu-modified zeolite, thereby oxidizing the reactant to provide an intermediate, and exposing the intermediate and a co-reagent to a second catalyst, thereby reacting the co-reagent with the intermediate to provide a product.
In some embodiments, a composition is described, the composition comprising a first catalyst comprising a Cu-modified zeolite, and a second catalyst capable of a coupling reaction between (a) an intermediate resulting from a reaction of a reactant at the first catalyst, and (b) a co-reagent, wherein a rate of diffusion of the co-reagent relative to the first catalyst is lower than a rate of diffusion of the intermediate relative to the first catalyst.
According to certain embodiments, a composition is described, the composition comprising a first catalyst comprising a Cu-modified zeolite, and a second catalyst capable of a coupling reaction between (a) an intermediate resulting from a reaction of a reactant at the first catalyst, and (b) a co-reagent, wherein a rate of diffusion of the co-reagent relative to the first catalyst is lower than a rate of diffusion of the co-reagent relative to the second catalyst.
Other advantages and novel features of the present invention will become apparent from the following detailed description of various non-limiting embodiments of the invention when considered in conjunction with the accompanying figures. In cases where the present specification and a document incorporated by reference include conflicting and/or inconsistent disclosure, the present specification shall control.

BRIEF DESCRIPTION OF THE DRAWINGS

Non-limiting embodiments of the present invention will be described by way of example with reference to the accompanying figures, which are schematic and are not intended to be drawn to scale unless otherwise indicated. In the figures, each identical or nearly identical component illustrated is typically represented by a single numeral. For purposes of clarity, not every component is labeled in every figure, nor is every component of each embodiment of the invention shown where illustration is not necessary to allow those of ordinary skill in the art to understand the invention.

In the figures:

FIG. 1 shows, according to certain embodiments, a schematic diagram of a catalytic composition for oxidizing a reactant;

FIG. 2 shows, according to certain embodiments, a flow diagram of a method of oxidizing a reactant to provide an intermediate and coupling the intermediate with a co-reagent;

FIG. 3A shows, according to some embodiments, a comparison of the total rates of product formation across temperature;

FIG. 3B shows, according to some embodiments, a comparison of the total rates of product formation across pressure;

FIG. 4A shows, according to some embodiments, a comparison of the total rates of conversion and product formation under partial methane oxidation flows;

FIG. 4B shows, according to some embodiments, a comparison of the total rates of conversion and product formation under benzene oxidation flows;

FIG. 5A shows, according to some embodiments, product selectivity versus conversion;

FIG. 5B shows, according to some embodiments, product formation rates versus P_CH4,

FIG. 5C shows, according to some embodiments, product formation rates versus P_O2;

FIG. 5D shows, according to some embodiments, product formation rates versus P_benzene;

FIG. 6 shows, according to some embodiments, a schematic of a hypothesized reaction pathway in the methane partial oxidation.; aromatic alkylation mixed system;

FIG. 7A shows, according to some. embodiments, a comparison of the total rates of product formation across temperature;

FIG. 7B shows, according to some embodiments, a comparison of the total rate of product formation across and pressure;

FIG. 8A shows, according to some embodiments, a comparison of rates of CH₄-to-CH₃OH over Cu-CHA-1 to tandem oxidation and alkylation over Cu-CHA-1/H-MFI-2 across temperature;

FIG. 8B shows, according to sorrre embodiments, a comparison of rates of CH₄-to-CH₃OH over Cu-CHA-1 to tandem oxidation and alkylation over Cu-CHA-1/H-MFI-2across pressure;

FIG. 8C shows, according to some embodiments, the selectivity for partially oxidized products versus conversion;

FIG. 8D shows, according to some embodiments, the observed CH₄conversion, selectivity, and product yield for tandem oxidation and alkylation over Cu-CHA/H-MFI;

FIG. 9A shows, according to sonic embodiments, a comparison of rates of product formation of Cu-CHA-1/H-MFI-2 and Cu-CHA-2/H-MFI-3;

FIG. 9B shows, according to some embodiments, a comparison of rates of product formation rates across multiple conditions over Cu-CHA-2/H-MFI-3;

FIG. 10.A shows, according to some embodiments, a scanning electron microscopy image of Cu-CHA-1;

FIG. 10B shows, according to some embodiments, a scanning electron microscopy image of H-MFI-1;

FIG. 11A shows, according to some embodiments, a powder X-ray diffraction pattern of Cu-CHA-1 and Cu-CHA-2;

FIG. 11B shows, according to sonic embodiments, a powder X-ray diffraction pattern of H-MFI-1 and H-MFI-2;

FIG. 12A shows, according to some embodiments, a table of parameters used for verification of absence of heat and mass transfer gradients;

FIG. 12B shows, according to some embodiments, a plot of CH₄conversion versus contact time for Cu-CHA-1 and H-MFI-2;

FIG. 13 shows, according to some embodiments, rates of product formation over Cu-CHA/H-MFI versus time-on-stream

FIG. 14A shows, according to some embodiments,qes of CO₂formation in the absence of catalyst across pressure;

FIG. 14B shows, according to some embodiments, rates of CO₂formation inthe absence of catalyst across temperature;

FIG. 15 shows, according to some embodiments, a comparison of tandem oxidation and alkylation rates from the addition of individual beds of Cu-CHA and H-MFI to an intimately mixed bed of Cu-CHA/H-MFI;

FIG. 16 shows, according to some embodiments, product formation rate dependence on P_O2for benzene oxidation in the absence of CH₄;

FIG. 17A shows, according to some embodiments, CO and ¹³CO and CO₂and ¹³CO₂signals under tandem oxidation and alkylation conditions and upon the introduction of ¹³C₆benzene at 543 K;

FIG. 17B shows, according to some embodiments, CO and ¹³CO and CO₂and ¹³CO₂signals under tandem oxidation and alkylation conditions and upon the introduction of ¹³C₆benzene at 603 K;

FIG. 18A shows, according to some embodiments, benzene and ¹³C₆H₆signals under tandem oxidation and alkylation conditions and upon the introduction of ¹³C₆benzene at 543 K

FIG. 18B shows, according to some embodiments, benzene and ¹³C₆H₆signals under tandem oxidation and alkylation conditions and upon the introduction of ¹³C₆benzene at 603 K.

DETAILED DESCRIPTION

Catalytic compositions and methods are generally described. In one aspect, a catalytic composition comprises a first catalyst and a second catalyst. The first catalyst may be capable of catalytically oxidizing a reactant to provide an intermediate, while the second catalyst may be capable of a coupling reaction between the intermediate and a co-reagent in a manner in which relative exposure of the co-reagent to the first and second catalysts is controlled. The coupling reaction may, in some embodiments, be an alkylation or an etherification reaction between the intermediate and the co-reagent. For example, in certain embodiments, the first catalyst catalytically oxidizes an alkane (e.g., methane) to an intermediate (e.g., methanol), and the second catalyst couples the reaction between the intermediate and a co-reagent (e.g., benzene) to provide a product (e.g., toluene).
Methane monooxygenases (MMOs) are selective for methane (CH₄) activation as a result of a gating mechanism that limits contact of methanol (CH3OH) with the metal (e.g., Cu) active site(s) in order to avoid over-oxidation of methanol to, for example, carbon dioxide (CO₂). The gating mechanism employed by MMOs has not been reproduced using conventional synthetic catalysts due to their relatively rigid nature. Furthermore, conventional synthetic methane oxidation systems operate stoichiometrically as opposed to catalytically. Described herein, however, are compositions and methods for chemical scavenging upon the activation of a reactant as a means of mimicking the gating system in MMOs.
In some embodiments, for example, the second catalyst, such as a solid acid catalyst, chemically scavenges the intermediate, such as methanol, which is a product of the catalytic reaction of the reactant at the first catalyst. The second catalyst may be configured to catalytically couple the chemically scavenged intermediate with a co-reagent, such as benzene, thereby providing a product, such as toluene. The rate of diffusion of the co-reagent relative to the first catalyst (e.g., within one or more cages and/or pores of the first catalyst) is lower than the rate of diffusion of the intermediate relative to the first catalyst (e.g., within the one or more cages and: or pores of the first catalyst). A composition comprising the first and second catalysts in such a configuration functions to exclude the co-reagent from entering the cages and/or pores of the first catalyst, thereby mitigating over-oxidation events at one or more active sties of the first catalyst and facilitating the coupling reaction between the scavenged intermediate and the co-reagent by the second catalyst.
While specific examples of catalysts, reactants, intermediates, etc. are used immediately above, those of ordinary skill in the art will recognize the applicability of the invention to many substrates, intermediates, reactants, co-reagents, etc. as will be described more fully further below.
In some embodiments, the tandem catalyst composition functions due to the following factors: (i) the second catalyst does not inhibit oxidation of the reactant (e.g., CH₄) by the first catalyst; (ii) the second catalyst and the product (e.g., toluene) are more resistant than the intermediate (e.g., CH₃OH) to undesirable over-oxidation (e.g., to CO₂); (iii) the rate of the reaction (e.g., the alkylation reaction) between the intermediate (e.g., CH₃OH) and the co-reagent (e.g., benzene) is not rate-limiting; and (iv) the distance that the intermediate (e.g., CH₃OH) diffuses (e.g., from the first catalyst to the second catalyst) is minimized to limit opportunities for undesirable over-oxidation of the intermediate (e.g., CH₃OH) by the first catalyst.
A non-limiting schematic diagram representing a catalytic composition for oxidizing a reactant is shown in FIG. 1. As shown in FIG. 1, composition 100 comprises first catalyst 102 and second catalyst 104. In some embodiments, first catalyst 102 is exposed to stream 106 comprising a reactant. As a result of exposing first catalyst 102 to stream 106 comprising the reactant, the reactant is catalytically oxidized to an intermediate. Second catalyst 104, in some embodiments, is exposed to the intermediate and stream 108 comprising a co-reagent. As a result of exposing second catalyst 104 to the intermediate and stream 108 comprising the co-reagent, the intermediate and the co-reagent are coupled to form stream 110 comprising a product.

Exposing Reactant to First Catalyst

In certain embodiments, methods of oxidizing a reactant are described. FIG. 2 shows, according to certain embodiments, a flow diagram of a method of oxidizing a reactant to provide an intermediate and coupling the intermediate with a co-reagent. As shown in FIG. 2, method 200 comprises step 202 wherein a reactant (e.g., methane) is exposed to a first catalyst (e.g., a Cu-modified catalyst). The reactant may be exposed to the first catalyst in the gaseous state, in some embodiments. According to certain embodiments, and as shown in step 204, the reactant is oxidized as a result of exposing the reactant to the first catalyst, thereby providing an intermediate (e.g., methanol). in certain embodiments, the intermediate is produced (e.g., from oxidation of the reactant by the first catalyst) in a continuous and/or catalytic process.
As used herein, the phrase “catalytic process” is given its ordinary meaning in the art and generally refers to a continuous process wherein, on average, more than one molecule of product is produced per a single active site of the catalyst. A catalytic process does not include the regeneration of the catalyst through a separate regeneration process. The phrase “stoichiometric process” is given its ordinary meaning in the art. as used herein and generally refers to a process in which only one molecule of product is produced per a single active site, wherein the active site is inactive following formation of the molecule of product. Thus, in contrast to a catalytic process, in order to produce more than one molecule of product per a single active site during a stoichiometric process, the active site must be regenerated through a separate regeneration process. In some embodiments, in which the precise number of active sites has not been fully determined, but has been limited to a particular class, such as moles of a particular metal (for example, copper), the total number of moles of that metal serve as a ceiling to the number of possible active sites. According to such embodiments, a process is catalytic where the moles of product generated exceed the moles of that metal (e.g., copper), without requiring a separate regeneration process.
The production of an intermediate (e.g., methanol) from a reactant (e.g., methane) is further described in U.S. Pat. No. 10,099,979, entitled “Catalytic Methods for the Production of an Alcohol from an Alkane”, which is incorporated herein by reference in its entirety for all purposes.

Reactant

As noted above, based on the disclosure herein relating to the provision of catalysts with general properties related to advantageous reactions involving reactants, intermediates, and co-reagents, those of ordinary skill in the art based on this disclosure will readily be able to select suitable catalysts and reagents from a wide range of species, and will be able to identify, without undue experimentation, which catalysts and reagents can be used in connection with the invention.
The reactant may be any of a variety of suitable substrates. According to certain embodiments, the reactant comprises an alkane represented by the for C_nH_2n+2. In some embodiments, for example, the reactant comprises methane, ethane, propane, or butane. Mixtures of reactant are also possible (e.g., the reactant comprises methane and ethane, for example). According to some embodiments, the reactant may be optionally substituted. For example, in certain embodiments, the reactant may be represented by the general formula R¹CH₃, wherein R¹is hydrogen, an unsubstituted alkyl group, or an optionally substituted alkyl group.
As used herein, the term “alkyl” is given its ordinary meaning in the art and refers to the radical of saturated aliphatic groups, including straight-chain alkyl groups, branched-chain alkyl groups, cycloalkyl (alicyclic) groups, alkyl substituted cycloalkyl groups, and cycloalkyl substituted alkyl groups. In some cases, the alkyl group may be a lower alkyl group, i.e., an alkyl group having 1 to 10 carbon atoms (e.g., methyl, ethyl, propyl, butyl, pentyl, hexyl, hepta), octyl, nonyl, or decyl). In some embodiments, a straight chain or branched chain alkyl may have 30 or fewer carbon atoms in its backbone, and, in some cases, 20 or fewer. In some embodiments, a straight chain or branched chain alkyl may have 12 or fewer carbon atoms in its backbone (e.g., C1-C12 for straight chain, C3-C12 for branched chain), 6 or fewer, or 4 or fewer. Thus, as used herein, the term “alkyl” includes straight, branched and cyclic alkyl groups.

First Catalyst

The first catalyst may be selected from any of a variety of suitable catalysts. In some embodiments, the first catalyst comprises a zeolite. As used herein, the term “zeolite” generally refers to a crystalline porous material having a framework of oxides comprising silicon and, optionally, aluminum and/or one or more additional elements (e.g., boron, gallium, and/or phosphorous). According to some embodiments, the zeolite comprises a silicate framework, an aluminosilicate framework, a silicoaluminophosphate framework, a borosilicate framework, a gallosilicate framework, or a zincosilicate framework. In certain embodiments, the zeolite comprises a framework comprising a trivalent metal.
Examples of zeolites that may be used as a framework of the first catalyst include, but are not limited to, AEI, AFX, mazzite (MAZ), mordenite (MOR), ferrierite, (FER), beta (BEA), chabazite (CHA), and mobil composition of matter (MCM). Other commercially or non-commercially available zeolites may also be implemented. In some embodiments, mixtures of zeolites may be implemented as the first catalyst.
According to some embodiments, a framework of the first catalyst may be charged (e.g., negatively charged). For example, in certain embodiments, the framework of the zeolite creates a charge imbalance that is compensated by counter cations. The framework of the first catalyst (e.g., zeolite) is generally anionic, and the counter cations that balance the charge of the anionic framework may be associated with the framework (e.g., on the surface of the first catalyst, within one or more pores of the framework). In some embodiments, the zeolite may be modified such that at least a portion of the counter cations associated with the framework are exchanged (e.g., with other counter cations), as desired for a particular application. In some embodiments, for example, the zeolite may be modified by at least partially exchanging one or more counter cations with a transition metal, thereby providing a modified zeolite. According to some embodiments, for example, the zeolite may be modified with Cu and/or Fe. Any of the above listed zeolite frameworks may be modified with a transition metal (e.g., Cu). The transition metal, in some embodiments, may be present within one or more cages and/or pores of the first catalyst. in certain non-Limiting embodiments, for example, the first catalyst comprises Cu-modified SSL-13.
The first catalyst may comprise any of a variety of suitable amounts of the transition metal used to modify the first catalyst. In certain embodiments, for example, the first catalyst comprises the transition metal used to modify the first catalyst in an amount greater than 0.1 wt. %, greater than 0.5 wt. %, greater than 1 wt. %, greater than 1.5 wt. %, greater than 2 wt. %, greater than 2.5 wt. %, greater than 3 wt. %, greater than 3.5 wt. %, greater than 4 wt. %, or greater than 4.5 wt. % based on the total weight of the first catalyst. In some embodiments, the first catalyst comprises the transition metal used to modify the first catalyst in an amount less than or equal to 5 wt. %, less than or equal to 4.5 wt. %, less than or equal to 4 wt. %, less than or equal to 3.5 wt. %, less than or equal to 3 wt. %, less than or equal to 2,5 wt. %, less than or equal to 2 wt. %, less than or equal to 1.5 wt. %, less than or equal to 1 wt. %, or less than or equal to 0.5 wt. % .% based on the total weight of the first catalyst. The amount of transition metal used to modify the first catalyst may be determined by elemental analysis techniques, such as inductively coupled plasma atomic emission spectroscopy (ICP-AES) and/or inductively coupled plasma mass spectrometry (ICP-MS).
According to certain embodiments, it may be beneficial to remove and/or exchange one or more metal sites on the surface of the first catalyst in order to inhibit over-oxidation events from occurring at the surface of the first catalyst. In some embodiments, for example, the surface of the first catalyst may be modified to reduce surface acidity and/or remove one or more metals in order to mitigate the reactant (e.g., CH₄) and/or the co-reagent (e.g., benzene) from over-oxidizing as the reactant and/or the co-reagent are exposed to one more compositions described herein. In some embodiments, for example, the surface of the first catalyst may be modified by dealumination of surface aluminum. Dealumination, in some embodiments, may be. achieved by dealuminating the first catalyst with an organic-structure-directing agent used during the synthesis of the first catalyst, which may be associated with the first catalyst after synthesis. In certain embodiments, the surface of the first catalyst may be modified by silylation.
According to certain embodiments, the first catalyst comprises a zeolite (e.g., a Cu-modified zeolite) comprising one or more cages and/or pores. As explained in further detail below, it may be advantageous, in some embodiments, to employ a zeo ate as the first catalyst with one or more cages and/or pores that are large enough to allow the reactant (e.g., methane) to diffuse into the one or more cages and/or pores of the zeolite, but small enough to exclude the co-reagent from diffusing into the one or more cages and/or pores of the zeolite. As a result, the co-reagent does not inhibit the selective oxidation of the reactant by the first catalyst. Furthermore, the co-reagent is not subject to over-oxidation by one or more active sites of the first catalyst since the co-regent is too large to diffuse into one or more the cages and/or pores of the first catalyst. In some embodiments, for example, the first catalyst is a zeolite comprising 8-member ring pores.
In certain embodiments, wherein the first catalyst is a zeolite, the zeolite may have any of a variety of suitable cage and/or pore sizes. In some embodiments, for example, the zeolite (e.g., Cu-modified zeolite) comprises cage and/or pores with an average characteristic dimension, such as an average diameter of the pore and/or cage.
In certain embodiments, the average characteristic dimension (e.g., average diameter) of the cages and/or pores of the zeolite is less than or equal to 5 angstroms, less than or equal to 4.5 angstroms, less than or equal to 4 angstroms, less than or equal to 3.5 angstroms, less than or equal to 3 angstroms, or less than or equal to 2.5 angstroms. In certain embodiments, the zeolite (e.g., Cu-modified zeolite) comprises cages and/or pores with an average characteristic dimension (e.g., average diameter) of greater than or equal to 2 angstroms, greater than or equal to 2.5 angstroms, greater than or equal to 3 angstroms, greater than or equal to 3.5 angstroms, greater than or equal to 4 angstroms, or greater than or equal to 4.5 angstroms. Combinations of the above recited ranges are. also possible (e.g., the zeolite comprises cages and/or pores with an average characteristic dimension of less than or equal to 5 angstroms and greater than or equal to 2 angstroms, the zeolite comprises cages and/or pores with an average characteristic dimension of less than or equal to 3.5 angstroms and less than or equal to 4.5 angstroms). Other ranges are also possible. Methods of determining the average diameter of the zeolite cages and/or pores include powder X-ray diffraction and scanning electron microscopy (SEM).

Oxidizing Agent and Solvent.

According to certain embodiments, the reactant is exposed to the first catalyst in the presence of an oxidizing agent and a solvent. In some embodiments, one of or both the oxidizing agent and the solvent may be in the gaseous state when exposed to the first catalyst. In certain embodiments, one or both of the oxidizing agent and the solvent may be exposed to the first catalyst concurrently with the reactant. Referring to FIG. 1, for example, stream 106 comprising the reactant may also comprise the oxidizing agent and/or the solvent. In some such embodiments, first catalyst 102 may be exposed to the reactant, the oxidizing agent, and the solvent via stream 106.
As used herein, the term “oxidizing agent” is given its ordinary meaning in the art and generally refers to a chemical species that has the ability to oxidize or increase the oxidation state of another chemical species. In the processes described herein, the oxidizing agent generally serves as an oxidizing source for the reaction of oxidizing the reactant (e.g., alkane) to the intermediate. Without wishing to be bound by theory, for example, the oxidizing agent may form a reactive species at the active site of the first catalyst (e.g., a copper-oxo site), thereby resulting in a catalytically active species that may oxidize the reactant to the intermediate. In some embodiments, prior to the exposing the reactant to the first catalyst, the first catalyst may be activated by exposing the catalyst to the oxidizing agent. According to some non-limiting embodiments, the oxidizing agent comprises dioxygen (O₂). Other non-limiting examples of an oxidizing agent include ozone (O₃), nitric oxide, nitrous oxide, and hydrogen peroxide. Alternative or additional oxidizing agents or a combination of oxidizing agents may be used, in some embodiments.
It may be advantageous, in certain embodiments, to utilize the solvent in order to diffuse the intermediate from the first catalyst to the second catalyst, resulting in chemical scavenging of the intermediate by the second catalyst, as explained herein in greater detail. In some non-limiting embodiments, the solvent comprises water (H₂O). In certain embodiments, the solvent comprises an alcohol, such as ethanol. Alternative or additional solvents or a combination of solvents may be used, in some embodiments.
Without wishing to be bound by theory, the oxidation of the reactant to the intermediate may occur at one or more active sites within the first catalyst, In some embodiments, for example, the oxidation of the reactant to the intermediate may occur at one or more active sites (e.g., active metal sites) within the first catalyst (e.g., Cu-modified zeolite). The one or more active sites within the first catalyst may be tolerant to both the oxidizing agent (e.g., O₂) and the solvent (e.g., H₂O), in sonic embodiments, resulting in the continuous operation of the active sites for performing the oxidation of the reactant without having to be separately reactivated and/or regenerated, therefore producing more moles of the intermediate than the total number of moles of the active site present in the first catalyst. As compared to conventional methods, the continuous catalytic operation of the first catalyst as described herein is in contrast with a stoichiometric process for oxidizing reactants (e.g., alkanes), which results in one or less than one molecule of oxidized product per active site, thereby requiring reactivation and/or regeneration of the active sites.

Intermediate

In some embodiments, the intermediate comprises an activated and/or oxidized reactant. For example, in certain embodiments, wherein the reactant is an alkane, the intermediate comprises an oxidized alkane. In some embodiments, the intermediate is a saturated alcohol. For example, in some embodiments, the intermediate may be represented by the general formula C_nH_2n+1OH. The intermediate may, in some embodiments, be thermodynamically stable. According to certain embodiments, the intermediate comprises methanol, ethanol, propanol, or butanol, any of which may be optionally substituted. in certain embodiments, mixtures of intermediates are also possible (e.g., the intermediate comprises methanol and ethanol, for example).
The intermediate may be formed with a high intermediate selectivity. As used herein, the term “intermediate selectivity” is defined as:
$S_{i} = \frac{C_{i} F_{i}}{\sum_{i = 1}^{N} C_{i} F_{i}}$
where S_iis the selectivity of intermediate i on a C-atom basis, C_iis the number of carbon atoms incorporated from the reactant into intermediate i, F_iis the molar flow rate of intermediate i, and ΣC_iF_iis the total molar flow rate of carbon of all products produced by the oxidizing reaction. Without wishing to be bound by theory, other products produced by the oxidizing reaction may include carbon monoxide (CO) and/or carbon dioxide (CO₂).
In some embodiments, the intermediate is formed with an intermediate selectivity greater than or equal to 70%, greater than or equal to 75%, greater than or equal to 80%, greater than or equal to 85%, greater than or equal to 90%, or greater than or equal to 95%. In certain embodiments, the intermediate is formed with an intermediate selectivity less than or equal to 99%, less than or equal to 95%, less than or equal to 90%, less than or equal to 85%, less than or equal to 80%, or less than or equal to 75%. Combinations of the above recited ranges are also possible (e.g., the intermediate is formed with an intermediate selectivity greater than or equal to 70% and less than or equal to 99%, the intermediate is formed with an intermediate selectivity greater than or equal to 80% and less than or equal to 85%). Other ranges are also possible.

Exposing Intermediate and Co-reagent to Second Catalyst

Referring to FIG. 2, according to some embodiments, method 200 comprises step 206 wherein the intermediate (e.g., methanol) and a co-reagent (e.g., benzene) are exposed to a second catalyst (e.g., a proton-form zeolite). In some embodiments, one or both of the intermediate and the co-reagent may be in the gaseous state when exposed to the second catalyst. In certain embodiments, and as shown in step 208, the intermediate reacts with the co-reagent as a result of exposing the intermediate and the co-reagent to the second catalyst, thereby providing a product (e.g., toluene). In certain embodiments, the product is produced (e.g., from a coupling reaction between the intermediate and the co-reagent) in a continuous and/or catalytic process.

Co-Reagent

The co-reagent may be any of a variety of suitable substrates. In some embodiments, the co-reagent comprises an aromatic, an alcohol, a cyclic compound, and: or an alkene, any of which may be optionally substituted. In some embodiments, non-limiting embodiments of co-reagents include, but are not limited to, benzene, naphthalene, anthracene, toluene, ethylbenzene, phenol, aniline, acetophenone, benzaldehyde, benzoic acid, benzonibile, xylene, mesitylene, durene, styrene, biphenyl, benzyl alcohol, cyclohexene, cyciohexanol, cyclohexanone, hexene, and butene isobutylene). Mixtures of co-reagents are also possible (e.g., the co-reagent comprises benzene and toluene, for example).
In certain embodiments, it may be beneficial to employ a co-reagent that has a lower rate of diffusion relative to the first catalyst than a rate of diffusion of the intermediate relative to the first catalyst. Utilizing a co-reagent that has a lower rate of diffusion relative to the first catalyst than a rate of diffusion of the intermediate relative to the first catalyst may advantageously inhibit the over-oxidation of the co-reagent at one or more active sites of the first catalyst, therefore facilitating the coupling reaction between the intermediate and the co-reagent at the second catalyst, which is explained in greater detail below. As used herein, “rate of diffusion” is given its ordinary meaning in the art and refers to the change in the concentration of a diffusing species over time. According to some embodiments, for example, the rate of diffusion of a species relative to the first catalyst may, for example, encompass the rate of diffusion of a species to a surface of the catalyst, the rate of diffusion of a species to one or more active sites of the. first catalyst, and/or the rate of diffusion of a species within one or more cages and/or pores of the first catalyst. In some embodiments, for example, the rate of diffusion of the co-reagent relative to the first catalyst is no more than 60%, no more than 50%, no more than 40%, no more than 30%, no more than 20%, no more than 10%, no more than 5%, or no more than 1% the rate diffusion of the intermediate relative to the first catalyst.
In some embodiments, the co-reagent has a lower rate of diffusion within the cages and/or pores of the first catalyst than a rate of diffusion of the intermediate within the cages and/or pores of the first catalyst. In some embodiments, for example, the rate of diffusion of the co-reagent within the cages and/or pores of the first catalyst is no more than 60%, no more than 50%, no more than 40%, no more than 30%, no more than 20%, no more than 10%, no more than 5%, or no more than 1% the rate diffusion of the intermediate within the cages and/or pores of the first catalyst.
In certain embodiments, the co-reagent has a lower rate of diffusion relative to the first catalyst than a rate of the diffusion of the co-reagent relative to the second catalyst. Advantageously, utilizing a co-reagent that has a lower rate of diffusion relative to the first catalyst than a rate of diffusion of the co-reagent relative to the second catalyst may promote the co-reagent to diffuse to one or more active sites of the second catalyst, therefore facilitating the coupling reaction between the co-reagent and the intermediate provided by the oxidation of the reactant at the first catalyst.
According to certain embodiments, and as mentioned above, the co-reagent may be chosen by one of ordinary skill in the art such that diffusion of the co-reagent into the. cages and/or pores of the first catalyst (e.g., the Cu-modified zeolite) is inhibited or prevented. For example, in some embodiments, a size of the co-reagent may be too large to diffuse into the cages and/or pores of the first catalyst (e.g., the Cu-modified zeolite). In certain embodiments, the co-reagent has an average characteristic dimension that is larger than the average characteristic dimension (e.g., average diameter) of the cages and/or pores of the first catalyst. In some embodiments, the average characteristic dimension of the co-reagent may be a kinetic diameter, an average length of the molecule, an average diameter of the molecule, and/or the like.
Although conventions for measuring the size of the co-reagent and ability of the co-reagent to access the first catalyst, for example, via passage through pores and/or cage openings (or inhibition thereof) is discussed, specific conventions for measurement are less important than the concept presented in this disclosure that inhibition or prevention of access to the first catalyst by the co-reagent is desired, in some embodiments. With the benefit of that concept, those of ordinary skill in the art will readily be able to measure co-reagents and design catalyst structures accordingly.
Control of inhibition of access to the first catalyst by the co-reagent is described herein via selection of a pore or cage structure of the catalyst. In another set of embodiments, an auxiliary filter or the like can be positioned between the source of the co-reagent and the first catalyst. For example, the first catalyst might not be porous or have a caged structure, but can be at least partially covered by a filter with, for example, the requisite porosity. In another set of embodiments, the first catalyst is porous, but an auxiliary filter is also provided. Based upon the conceptual discussion herein, those of ordinary skill in the art can readily select appropriate filters, for example, molecular sieves, metal-organic frameworks, other filters of appropriate porosity, etc. In this arrangement, all that is needed is that the filter and/or the cage structure or porosity of the catalyst, alone or together, inhibits or prevents contact of the first catalyst by the co-reagent as desired.
In some embodiments, the average characteristic dimension (e.g., kinetic diameter) of the co-reagent is greater than or equal to 4.5 angstroms, greater than or equal to 5 angstroms, greater than or equal to 5.5 angstroms, greater than or equal to 6 angstroms, or greater than or equal to 6.5 angstroms. In some embodiments, the average characteristic dimension (e.g., kinetic dimeter) of the co-reagent is less than or equal to 7 angstroms, less than or equal to 6.5 angstroms, less than or equal to 6 angstroms, less than or equal to 5.5 angstroms, or less than or equal to 5 angstroms. Combinations of the above recited ranges are also possible (e.g., the average characteristic dimension of the co-reagent is greater than or equal to 4.5 angstroms and less than or equal to 7 angstroms, the average characteristic dimension of the co-reagent is less than or equal to 6 angstroms and greater than or equal to 5.5 angstroms). Other ranges are also possible.

Second Catalyst

The second catalyst may be selected from any of a variety of suitable catalysts. According to certain embodiments, the second catalyst is capable of a coupling reaction. The coupling reaction, in certain embodiments, is a reaction between the intermediate resulting from the reaction of the reactant at the first catalyst, and the co-reagent. In some embodiments, for example, the second catalyst is capable of coupling the co-reagent and the intermediate. Sonic non-limiting examples of coupling reactions include, for example, alkylation and/or etherification.
In some embodiments, the second catalyst is a solid acid catalyst. For example, in certain embodiments, the solid acid catalyst may comprise one or more Bronsted acid sites and display Bronsted acid characteristics. Without wishing to be bound by theory, in some embodiments, the coupling reaction occurs at the one more Bronsted acid sites within the second (e.g., solid acid) catalyst. In certain embodiments, the Bronsted acid sites comprise a plurality of catalytically active acidic hydroxyls, for example. The second catalyst may comprise, in some embodiments, a zeolite, a metal oxide, a metal-organic-framework (MOF), a heteropoly acid, a polyoxometallate, sulfated zirconia, hypophosphorous acid, aluminophosphate (AIPO), silicoaluminophosphate (SAPO), and/or combinations thereof.
The metal oxide may comprise, in some embodiments, alumina, silica, molybdenum oxide, tungsten oxide and/or the like. In some aspects, the metal oxide may be treated and/or untreated. In certain embodiments, the metal oxide may be associated with a support, such as an aluminosilicate support.
In certain embodiments, the second catalyst comprises a zeolite (e.g., a proton-form zeolite). According to some embodiments, the zeolite comprises a silicate framework, an aluminosilicate framework, a silicoaluminophosphate framework, a borosilicate framework, a gallosilicate framework, or a zincosilicate framework. According to certain embodiments, the zeolite comprises framework comprising a trivalent metal.
Examples of zeolites that may be used as a framework of the second catalyst include, but are not limited to, ZSM-5, ZSM-22, SSZ-33, and/or beta (BEA). According to certain non-limiting embodiments, for example, the second catalyst comprises ZSM-5. Other commercially or non-commercially available zeolites may also be implemented.
According to certain embodiments, one or more metal sites on the surface of the second catalyst may be exchanged and/or removed to inhibit over-oxidation events from occurring at the surface of the second catalyst. In some embodiments, for example, the surface of the second catalyst may be modified to reduce surface acidity and/or remove one or more metals in order to mitigate the reactant (e.g., CH₄) and/or the co-reagent (e.g., benzene) from over-oxidizing as the reactant and/or the co-reagent are exposed to one more compositions described herein. In some embodiments, for example, the. surface of the second catalyst be modified by dealumination of surface aluminum. Dealutnination, in some embodiments, may be achieved by dealuminating the second catalyst. In certain embodiments, the surface of the second catalyst may he modified by silylation.

Product

In certain embodiments, the product comprises a reaction product (e.g., coupled reaction product) between any of the aforementioned intermediates and any of the aforementioned co-reagents. In certain embodiments, for example, the product comprises an alkylated product resulting from the coupling reaction between the intermediate (e.g., methanol) and the co-reagent (e.g., benzene). in some embodiments, for example, the product comprises toluene, xylene (e.g., ortho-, meta-, and/or para-xylene), or anisole. As would be understood by a person of ordinary skill in the art, other products are possible depending on the choice of intermediate and co-reagent, as explained in further detail above. Mixtures of products are also possible, in some embodiments (e.g., the product comprises toluene and xylene).
The product may be formed with a high product selectivity. As used herein, the term “product selectivity” is defined as:
$S_{i} = \frac{C_{i} F_{i}}{\sum_{i = 1}^{N} C_{i} F_{i}}$
where S_iis the selectivity of product i on a C-atom basis, C_iis the number of carbon atoms incorporated from the reactant into product i, F_iis the molar flow rate of product i, and ΣC_iF_iis the total molar flow rate of carbon of all products. Without wishing to be bound by theory, other products produced may include carbon monoxide (CO) and/or carbon dioxide (CO₂).
In some embodiments, the product is formed with a product selectivity greater than or equal to 70%, greater than or equal to 75%, greater than or equal to 80%, greater than or equal to 85%, greater than or equal to 90%, or greater than or equal to 95%. In certain embodiments, the product is formed with a product selectivity less than or equal to 99%, less than or equal to 95%, less than or equal to 90%, less than or equal to 85%, less than or equal to 80%, or less than or equal to 75%. Combinations of the above recited ranges are also possible (e.g., the product is formed with a product selectivity greater than or equal to 70% and less than or equal to 99%, the product is formed with a.
product selectivity greater than or equal to 80% and less than or equal to 85%). Other ranges are also possible.
The product may be formed with a high reactant conversion percentage. As used herein, the term “conversion percentage” is defined as:
$X_{R} = \frac{\sum_{i = 1}^{N} C_{i} F_{i}}{F_{R}}$
where X_Ris the conversion of reactant, F_iis the molar flow rate of product i, C_iis the number of carbon atoms incorporated from the reactant into product i, ΣC_iF_iis the total molar flow rate of carbon of all products, and F_Ris the initial molar flow rate of reactant.
In certain embodiments, the product is formed with a reactant conversion percentage greater than or equal to 0.1%, greater than or equal to 0.2%, greater than or equal to 0.3%, greater than or equal to 0,4%, greater than or equal to 0.5%, greater than or equal to 0.6%, greater than or equal to 0.7%, greater than or equal to 0.8%, greater than or equal to 0.9%, or greater than or equal to 1%. In some embodiments, the product is formed with a reactant conversion percentage less than or equal to 1.5%, less than or equal to 1%, less than or equal to 0.9%, less than or equal to 0.8%, less than or equal to 0.7%, less than or equal to 0.6%, less than or equal to 0.5%, less than or equal to 0.4%, less than or equal to 0.3%, or less than or equal to 0.2%. Combinations of the above recited ranges are also possible (e.g., the product is formed with a reactant conversion percentage greater than or equal to 0.1% and less than or equal to 1.5%). Other ranges are also possible.

Reaction Conditions

The ratio (e.g., molar ratio) of the first catalyst and the second catalyst may be any of a variety of suitable ratios. In certain embodiments, for example, the ratio (e.g., weight ratio) of the first catalyst to the second catalyst is greater than or equal to 0.1:1, greater than or equal to 0.2:1, greater than or equal to 0.3:1, greater than or equal to 0.4:1, greater than or equal to 0.5:1, greater than or equal to 1:1, greater than or equal to 2:1, greater than or equal to 3:1, greater than or equal to 4:1, or greater than or equal to 5:1. In some embodiments, the ratio (e.g., weight ratio) of the first catalyst to the second catalyst is less than or equal to 5:1, less than or equal to 4:1, less than or equal to 3:1, less than or equal to 2:1, less than or equal to 1:1, less than or equal to 0.5:1, less than or equal to 0.4:1, less than or equal to 0.3:1, less than or equal to 0.2:1, or less than or equal to 0.1:1. Combinations of the above recited ranges are also possible (e.g., the weight ratio of the first catalyst to the second catalyst is greater than or equal to 0.1:1 and less than or equal to 5:1). Other ranges are also possible.
In certain non-limiting embodiments, it may be advantageous to employ a greater amount of the second catalyst in order to minimize the intermediate diffusion pathway from the first catalyst to the second catalyst. In some embodiments, minimizing the diffusion pathway decreases the number of over-oxidation events of the intermediate caused by the first catalyst. In sonic such embodiments, the ratio (e.g., weight ratio) of the first catalyst to the second catalyst may be greater than 0.1:1 and less than 1:1.
In some embodiments, the first catalyst and the second catalyst are a mixture. According to certain embodiments, for example, the first catalyst and the second catalyst may be mixed by vortexing the first catalyst and the second catalyst as powders. The mixed powders of the first catalyst and the second catalyst may be pelletized (e.g., after mixing), in some embodiments.
In certain embodiments, the mixture of the first catalyst and the second catalyst (e.g., pelletized mixture) may be placed in an apparatus suitable for carrying out the catalytic reactions. In some embodiments, for example, the first catalyst and the second catalyst may be placed in a reactor (e.g., a catalyst reactor bed). Referring to FIG. 1, for example, first catalyst 102 and second catalyst 104 may be placed in rector 112, in some embodiments. According to certain embodiments, both the first catalyst and the second catalyst are concurrently exposed to the reactant and the co-reagent (e.g., in the gaseous state). For example, referring to FIG. 1, composition 100 may comprise a mixture of first catalyst 102 and second catalyst 104, and said mixture is concurrently exposed to stream 106 comprising a reactant and stream 108 comprising a co-reagent. In some embodiments, stream 106 and/or stream 108 may be introduced to reactor 112 from a single inlet or from multiple inlets, Stream 106 and/or stream 108 may, in some efribodiments, be introduced to the reactor continuously, for example, when the reactor is operating in a continuous mode, and a continuous reaction is taking place. According to some embodiments, the reactor may be sealed to an external atmosphere, in which no new matter enters or exits the reactor during operation in a hatch mode.
The step of exposing the reactant to the first catalyst and: or the step of exposing the intermediate and the co-reagent to the second catalyst may occur at any of a variety of temperatures. In some embodiments, one or both of the exposing steps are performed at a temperature greater than or equal to 100° C., greater than or equal to 150° C., greater than or equal to 200° C., greater than or equal to 250° C., greater than or equal to 300° C., greater than or equal to 350° C., greater than or equal to 400° C., or greater than or equal to 450° C. In certain embodiments, one or both of the exposing steps are performed at a temperature less than or equal to 500° C., less than or equal to 450° C., less than or equal to 400° C., less than or equal to 350° C., less than or equal to 300° C., less than or equal to 250° C., less than or equal to 200° C., or less than or equal to 150° C. Combinations of the above recited ranges are also possible (e.g., one or both of the exposing steps are performed at a temperature greater than or equal to 100° C. and less than or equal to 500 ° C., one or both of the exposing steps are performed at a temperature greater than or equal to 200° C., and less than or equal to 400 ° C.). Other ranges are also possible.
The step of exposing the reactant to the first catalyst and/or the step of exposing the intermediate and the co-reagent to the second catalyst may occur at any of a variety of pressures. In some embodiments, one or both of the exposing steps are performed at a pressure greater than or equal to 1 bar, greater than or equal to 5 bar, greater than or equal to 10 bar, greater than or equal to 15 bar, greater than or equal to 20 bar, greater than or equal to 25 bar, greater than or equal to 30 bar, or areater than or equal to 35 bar. In certain embodiments, one or both of the exposing steps are performed at a pressure less than or equal to 40 bar, less than or equal to 35 bar, less than or equal to 30 bar, less than or equal to 25 bar, less than or equal to 20 bar, less than or equal to 15 bar, less than or equal to 10 bar, or less than or equal to 5 bar. Combinations of the above recited ranges are also possible (e.g., one or both of the exposing steps are performed at a pressure greater than or equal to 1 bar and less than or equal to 40 bar, one or both of the exposing steps are performed at a pressure greater than or equal to 5 bar and less than or equal to 15 bar).
The following example is intended to illustrate certain embodiments of the present invention, but does not exemplify the full scope of the invention.

EXAMPLE 1

The following examples describes the oxidation of a reactant by a first catalyst to provide an intermediate, and the coupling reaction of the intermediate with a co-reagent facilitated with a second catalyst.
Cu-SSZ-13 catalysts (denoted Cu-CHA) were synthesized to contain no Na and an abundance of Al to facilitate active site formation, and Cu content was chosen so that Cu/cage<0.3 to avoid the formation of undesirable Cu oxides. H-ZSM-5 (denoted H-MFI) was synthesized to contain no Fe and an abundance of Al, and thereby protons, to enable benzene alkylation. The compositions of some non-limiting catalysts are summarized in Table 1. SEM images Cu-CHA-1 and H-MFI -1 are shown in FIGS. 10A and 10B, respectively. X-ray diffraction patterns of Cu-CHA-1/Cu-CHA-2 and H-MFI-1/H-MFI-2 are shown in FIGS. 11A and 11B, respectively.

TABLE 1

Composition of Cu-CHA and H-MFI catalysts.

		Cu
	Composition	Content

Catalyst	Si/Al	Cu/Al	(wt %)

Cu-CHA-1	11	0.13	1.1
Cu-CHA-2	13	0.13	0.9
H-MFI-1	19	—	—
H-MFI-2	16	—	—
H-MFI-3	15	—	—

To minimize the number of downstream over oxidation events from CH₄to CH₃OH to CO₂, the diffusion path of CH₃OH was minimized by combining Cu-CHA and H-MFI with a larger amount of H-MFI than Cu-CHA (e.g., 1:3 Cu-CHA:H-MFI by weight, denoted Cu-CHA/H-MFI). Cu-CHA and H-MFI were intimately mixed by vortexing the fine powders together prior to pelletizing.
FIGS. 3A-3B demonstrate that both Cu-CHA and H-MFI were significant for toluene formation across all temperatures and pressure studied. For FIGS. 3A-3B, catalyst composition and the alkylation feed mixture was 0.2625 g H-MFI-1, 0.0875 g Cu-CHA-1, and (0.0875 g Cu-CHA-1+0.2625 g H-MIF-2), 26.1 sccm, x_CH4=0.18, xC₆H₆=0.008, xO₂=0.001, P_H2O=3.1 kPa, bal He, where x indicates mole fraction. When pressurizing, water partial pressure remained unchanged because it was introduced by a saturator, while other reactants increased proportionally. The reaction schematic shown above FIGS. 3A and 3B demonstrates potential sources of product formation based where C's are indicative of source of C (CH₄or benzene) for observed products.
Reaction rates were measured in the absence of heat and mass transfer limitations (see FIGS. 12A-12B). For FIG. 12B, the catalyst composition and feed mixture was (0.0875 g Cu-CHA−1+0.2625 g H-MFI-2), 543 K, 1 bar, 26.1−209 sccm, P_CH4=18 kPa, P_O2=0.09 kPa, P_H2O=3.1 kPa, P_C6H6=0.80 kPa, bal He. Stable and repeatable product formation rates were observed for at least 12 hours on stream (see FIG. 13).
FIG. 13 demonstrates that stable rates were observed for at least 12 hours. For FIG. 13. the catalyst composition and feed mixture was (0.0875 g Cu-CHA-1+0.2625 g H-MFI-2), 543 K, 26.1 sccm, xCH₄=0.008, xC₆H₆=0.008, xO₂=0.001, P_H2O=3.1 kPa, bal He. Catalysts were calcined at 823 K under dry air for 8 hours prior to testing. Rates of product formation were presented as the absolute rates observed to enable direct comparison of these three catalysts. The catalyst loading of the individual H-MFI and Cu-CHA catalysts beds were the same as in the intimately mixed catalyst bed. Toluene was not observed in the absence of catalyst under the same feed and reactor conditions (see FIGS. 14A and 14B). For FIGS. 14A-14B, the feed mixture was 26.1 sccm, xCH₄=0.18, xC₆H₆=0.008, xO₂=0.001, P_H2O=3.1 kPa, bal He where x indicates mole fraction. When pressurizing, water partial pressure remained unchanged because water is introduced by a saturator, all other reactants increased proportionally. In the absence of either Cu-CHA or H-MFI, low rates of toluene formation were observed over H-MFI for P>1 bar and over Cu-CHA for T≥633 K or P>1 bar (see FIGS. 3A-3B). These rates of formation of toluene were much lower than those observed over Cu-CHA/H-MFI. It was hypothesized that the observed toluene formation over Cu-CHA was a result of surface protons catalyzing aromatic alkylation since benzene cannot access the pores of Cu-CHA.
Upon closer inspection of FIGS. 3A-3B, the total rate of product formation was consistently higher over Cu-CHA/H-MFI than over either H-MFI or Cu-CHA or the addition of the rates of production formation over each of H-MFI and Cu-CHA (see FIG. 15). For FIG. 15, the catalyst composition and feed mixture was 0.2625 g H-MFI-1, 0.0875 g Cu-CHA-1, and (0.0875 g Cu-CHA-1+0.2625 g H-MFI-2), 26.1 sccm, xCH₄=0.18, xC₆H₆=0.008, xO₂=0.001, P_H2O=3.1 kPa, bal He. FIG. 15 demonstrates that across all temperatures, there is a greater rate of product formation for Cu-CHA/H-MFI than from the addition of the rates of product formation over individual Cu-CHA and H-MFI beds. It was hypothesized that the oxidation of benzene to CO and CO₂contributed to these observed rates, in addition to the already expected over oxidation of CH₄to CO₂. Thus, while the rate of toluene formation over Cu-CHA/H-MFI was similar to the total rate of product formation over Cu-CHA, a direct comparison could not be made due to differing amounts of CO and CO₂stemming from benzene over these catalysts. To study complete CH₄and benzene oxidation reactions in greater detail, the rates of product formation were observed over the same catalyst beds in the absence of benzene and CH₄, respectively.
FIG. 4A demonstrates that, in the absence of benzene (feeding CH₄/H₂O/₂), the activation of the C—H bond of CH₄originates primarily over Cu-CHA. Across all temperatures, the total rate of C-H activation was similar between Cu-CHA and Cu-CHA/H-MFI. Further, the rate of C—H activation over MFI was negligible over 543-663 K, in comparison to the rates of C—H activation versus Cu-CHA. The absence of significant CH₃OH formation between Cu-CHA and Cu-CHA/H-MFI was attributed to the added catalyst through which CH₃OH travelled, increasing the probability of over oxidation events occurring homogeneously or over H-MFI.
FIG. 4B demonstrates how benzene oxidation contributes to the rates of CO and CO₂formation in the absence of CH₄(feeding C₆H₆/H₂O/O₂). Across all three catalyst beds, CO and CO2 were the primary products observed. Because these rates of product formation were on similar scales to those observed when co-feeding CH₄/H₂O/O₂(see FIG. 4A), the contribution of benzene oxidation to CO and CO₂product formation rates under tandem oxidation and alkylation conditions was considered. It was unknown to what extent Cu-CHA and H-MFI each contributed to the observed rates of product formation over Cu-CHA/H-MFI because the sum of the rates over the individual catalyst beds of H-MFI and Cu-CHA was not equal to the rates over Cu-CHA/H-MFI. The catalyst composition and feed mixture in FIGS. 4A-4B was 0.2625 g H-MFI-1, 0.0875 g Cu-CHA-1, and (0.0875 g Cu-CHA-1 0.2625 g P=1 bar, 26.1 sccm, P_CH4=18 kPa, P_O2=0.09 kPa, PH₂O=3.1 kPa,=0.80 kPa, bal. He. The reaction schematics shown above FIGS. 4A-4B demonstrate potential sources of product formation based where C's are indicative of source of C (CH₄or benzene) for observed products.
Given the significance of benzene oxidation, an isotope switching experiment with ¹³C₆H₆under tandem oxidation and alkylation conditions (co-feed of CH₄/O₂/H₂O/C₆H₆) over Cu-CHA/H-MFI revealed benzene oxidation was the primary source of CO and accounted for more CO₂as temperature increased. At 543 K and 1 bar, benzene accounted for 85% of CO and 19% of CO₂observed. At 603 K and 1 bar, benzene accounted for 85% of CO and 42% of CO_2.These results were used to remove the contribution of benzene oxidation to CO and CO₂formation rates over Cu-CHA/H-MFI and enable direct comparison of the rates of product formation from CH₄-to-CH₃OH over Cu-CHA to the rates of product formation from tandem oxidation and alkylation over Cu-CHA/H-MFI. Kinetic data in combination with these results was used to estimate the contribution of benzene oxidation at conditions not specifically tested.
To gain further insight into the origins of product formation and the role of each reactant during tandem partial oxidation and alkylation, kinetic experiments at 543 K were completed by varying the total flow and partial pressures of CH₄, O₂, and benzene fed to Cu-CHA/H-MFI (see FIGS. 5A-5D). The catalyst composition and feed mixture in FIGS. 5A-5D was (0.0875 g Cu-CHA-1+0.2625 g H-MFI-2), T=543 K, P=1 bar, 26.1 sccm, 3.2 kPa H₂O, 0.09 kPa O₂, 18 kPa CH₄, 0.80 kPa benzene, bal He, except as noted. Analysis of a plot of selectivity versus conversion demonstrated product formation proceeded by a combination of sequential and parallel reaction pathways (FIG. 5A). The parallel reaction pathway was plausibly attributed to two sources: (1) parallel formation of CO₂from benzene and (2) parallel formation of CO₂and toluene from CH₃OH. The presence of a sequential pathway is consistent with CH₄activation first proceeding to CH₃OH and then to toluene and CO_2.Based on this reaction pathway, at low conversion, increasing selectivity to CO₂with decreasing CH₄conversion is explained by the persistence of oxidation of benzene to CO₂while the rates of CO₂and toluene formation from CH₃OH have decreased as a result of the reduced accumulation of methanol.
CH₄and O₂partial pressure analyses over Cu-CHA/H-MFI revealed C—H scission of CH₄was Fate-determining and the relatively fast interception of CH₃OH with benzene prior to over oxidation to CO₂(FIGS. 5B and 5C, respectively). A near first order dependence of the rate of toluene formation on P_CH4implied C—H scission of CH₄as the rate-determining step. A0.4 order dependence for the rate of CO₂formation on P_O2was consistent with the relatively fast interception of CH₃OH by benzene as compared to over oxidation to CO₂because this order dependence was less than the observed first order dependence of the rate of CO₂formation on P_O2under methanol synthesis conditions over Cu-CHA. Finally, a zero-order dependence of the rates of product formation on P_benzene(see FIG. 5D) demonstrated benzene alkylation was not rate-limiting nor inhibiting reaction pathways that were necessary to allow for the formation of CH₃OH. These observations are summarized by the proposed reaction pathway in FIG. 6, where initial CH₄activation forms CH₃OH that can either alkylate benzene to form toluene or be over oxidized to form CO₂. CO₂is also formed via benzene oxidation in a parallel pathway. Deleterious CO₂formation from methanol oxidation is minimized by intermediate scavenging to form alkylated aromatics, thus decreasing CO₂yields, and direct benzene oxidation pathways can be mitigated by modification of catalyst morphology and gas phase compositions. CO formation is hypothesized to form by the same reaction pathways as CO₂.
Next, placing separate beds of Cu-CHA and H-MFI in series separated by quartz wool demonstrated that intimate mixing of Cu-CHA and H-MFI obtained the optimum selectivity (see FIGS. 7A-7B). Tn FIGS. 7A-7B, “Cu-CHA+H-MFI” corresponds to the addition of rates of individual beds of Cu-CHA and H-MFI where these catalysts were tested separately, “Large gap” corresponds to a 3 cm quartz wool plug between beds, and “Small gap” corresponds to a 1 cm quartz wool plug. (0.0875 g Cu-CHA-1 and 0.2625 g H-MFI-2), 26.1 sccm, xCH₄=0:18, xC₆H₆=0.008, xO₂=0.001, P_H2O=3.1 kPa, bal He, where x indicates mole fraction. When pressurizing, water partial pressure remained unchanged because it was introduced by a saturator, while other reactants increased proportionally. The reaction schematics above FIGS. 7A and 7B demonstrate potential sources of product formation based where C's are indicative of source of C (CH₄or benzene) for observed products.
The rates of production formation over separate beds in series were compared to intimately mixed Cu-CHA and H-MFI and to the simple addition of product formation rates from individual. Across a range of temperature and pressures, two things stood out. as the two catalyst beds were brought into closer contact: (1) the rate of toluene formation increased and (2) the rates of CO₂and CO formation decreased. Consequently, intimately mixed Cu-CHA and H-MFI yielded the highest toluene selectivity of all catalyst configurations under identical conditions. These observations were rationalized by the increased distance CH3OH must be transported to be brought into contact with H-MFI with the separated beds, thereby increasing the number of homogeneous over oxidation events of CH₃OH and reducing the amount of CH₃OH available for benzene alkylation.
Based upon the intimate mixing of Cu-CHA and H-MFI and knowledge of the origins of each product, CH₄-to-CH₃OH conversion over Cu-CHA was compared to CR₄-to-CH₃OH-to-toluene conversion over Cu-CHA/H-MFI (see FIGS. 8A-8C) to demonstrate the efficacy of methanol scavenging. The results of the isotope labeling experiment plus kinetic experiments were used to remove the contribution of benzene, to CO2 and CO formation rates in the tandem partial oxidation and alkylation system. First, FIGS. 8A and 8B demonstrate there was good agreement between the total rates of product formation over Cu-CHA and Cu-CHA/H-MFI, consistent with CH₄activation occurring primarily over Cu-CHA as previously discussed, and enabling facile observation of the improvement in desirable product selectivity under tandem partial oxidation and alkylation conditions. In FIGS. 8A-8B, the numbers above each bar are the carbon-weighted selectivities for partial oxidation products. The slight differences in the total rate of C—H activation may have been a result of slight variations in Cu content between catalyst beds. The improvement in partial oxidation selectivity was highlighted at 663 K and 1 bar where there was 84% selectivity for toluene over Cu-CHA/H-MFI, in contrast to 2% selectivity for CH₃OH over Cu-CHA. The high selectivity for toluene at increasing conversion was indicative of the relatively fast scavenging of CH₃OH by toluene versus thermodynamically favorable deleterious over oxidation events with free gaseous CH₃OH.
Increasing pressure for catalytic CH₄-to-CH₃OH conversion resulted in a small decrease in selectivity for CH3OH (see FIG. 8B), which was in contrast to stoichiometric processes where selectivity is often minimally affected. However, increasing pressure under tandem oxidation and alkylation conditions over Cu-CHA/H-MFI improved selectivity from 70% to 89%. This improved selectivity was explained by analysis of the total dependence on reactant partial pressures for each product (e.g., with r_product˜P_CH4 ^aP_O2 ^b, the total order dependence is a+b). Because toluene had a total dependence of 0.94 versus 0.54 for CO₂, increasing the pressure increased the rate of toluene formation 75% more than the rate of CO₂formation. In contrast, the rate of methanol formation had a total order dependence of 1.03 versus 1.14 for the rate of CO₂formation under CH₄-to-CH₃OH conditions over Cu-SSZ-13, consequently slightly favoring CO₂formation at elevated pressures. Thus, under tandem partial oxidation and alkylation conditions, pressure provided another variable for optimizing process conditions for selective CH₄oxidation that would otherwise be unavailable.
Based on these favorable results, plotting partial oxidation selectivity versus conversion demonstrated that the selectivity-conversion limit of CH₄was circumvented by scavenging methanol (see FIG. 8C). In FIG. 8C, the “open circles” were previously reported, “solid circles” were from the compositions reported herein and generated by varying temperature and pressure as in FIG. 8A and FIG. 8B over 0.0875 g Cu-CHA-1. “Solid stars” were generated by altering temperature, pressure, total flow rate, catalyst loading and P_O2over (0.0875 g Cu-CHA-1+0.2625 g H-MFI-1), (0.0875 g Cu-CHA-1+0.2625 g H-MFI-2), and (0.366 g Cu-CHA-2+1097 g H-MFI-3). “Open stars” increased P_O2by 3 x and 5 x. Baseline flow conditions: 26.1 sccm, xCH₄=0.18, xC₆H₆=0.008, xO₂=0.001, P_H2O=3.1 kPa, bal He, where x indicates mole fraction. When pressurizing, water partial pressure remained unchanged because it was introduced by a saturator, while other reactants increased proportionally.
Data points presented were generated by altering contact time, temperature, pressure, and catalyst loading, as shown in FIG. 8D. Rates of product formation with increased catalyst loading are presented in FIGS. 9A-9B. P_O2was increased by 3x and 5x for the points at 0.3% and 0.6% CH₄conversion, respectively Immediately apparent was above 0.01% CH₄conversion, selectivity for toluene was at least 80% while selectivity for CH₄-to-CH₃OH over Cu-CHA dropped to <60%. It was hypothesized that the low selectivity for toluene observed below 0.01% CH₄conversion was a result of the low rates of CH₃OH formation at these conditions where the competition between over oxidation of CH₃OH to CO₂versus its diffusion to Brønsted acid sites in H-MFI became important. Implementation of a tandem partial oxidation and alkylation system enabled these results to surpass previously reported results for selectivity versus CH₄conversion at mild conditions, while only requiring readily available O₂and H₂O for CH₄activation.
These results warranted comparison to the best performing stoichiometric processes for CH₄-to-CH₃OH conversion over Cu-exchanged zeolites and to other heterogeneous CH₄-to-CH₃OH systems. Conventional systems have reported the optimization of an isothermal stoichiometric process over a Cu-FAU zeolite (Si/Al=2.6, Cu/Al=0.41, Cu wt. %=9.32) where the catalyst was first activated for 1 hour under O₂and then exposed to CH₄for 1 hour. Following, methanol was &sorbed for 1 hour at 633 K with water vapor. Taking this process as a 3 hour cycle time, the optimized methanol yield was 2 μmol ci_CH3OHmin⁻¹g_cat ⁻¹(˜1400μmol_CH3OH ⁻¹min⁻¹, 93% selectivity). In comparison, the results reported herein are a greater yield for tandem oxidation and alkylation of 2.7 μmol _{Toluene+Xylene}min⁻¹g_Cu-CHA ⁻¹at 603 K and 11 bar (74% selectivity for toluene and xylene combined). Additionally, the Cu loading was an order of magnitude lower than that used for the optimized stoichiometric process, giving a rate of formation of 19,000 μmol_CH3OHmol_Cu ⁻¹min⁻¹that far exceeded the 1400 μmol_CH3OHmol_Cu ⁻¹min⁻¹reported for the optimized stoichiometric process.
This conversion and yield for tandem oxidation and alkylation was also comparable to the best performing heterogeneous catalysts for CH₄-to-CH₃OH conversion. Greater than 75% CH₃OH selectivity has been reported for heterogeneous catalysts at <2% CH₄conversion. However, with the exception of Cu-exchanged zeolites, the remaining heterogeneous catalysts required expensive oxidants such as H₂O₂or N₂O or extreme conditions (e.g., P>140 bar), but the system reported herein simply required O₂, H₂O, and benzene as additional reactants and H-MFI as an additional catalyst at relatively mild conditions in comparison to these processes.
As demonstrated herein, the viability of product protection for CH₄activation was achieved by first activating CH₄over Cu-exchanged zeolites to produce CH₃OH and then capturing CH₃OH by aromatic alkylation over a proton-form zeolite. Control reactions and isotopically labeled benzene experiments demonstrated that benzene oxidation occurred in parallel to methane activation and contributed to the observed CO and CO₂formation rates. Upon accounting for benzene oxidation, the rates of CH₄activation were comparable between Cu-CHA and Cu-CHA/H-MFI across all conditions, but selectivity for desirable products was markedly improved by chemically scavenging methanol. High selectivity towards desirable products was maintained, even above 0.1% CH₄conversion where selectivity for CH₄-to-CH₃OH processes deteriorate. A toluene and xylene, yield of 2.7 μmol_{Toluene+Xylene}min⁻¹gCu-CHA⁻¹at 603 K and 11 bar was determined, which was greater than an optimized stoichiometric CH₄-to-CH₃OH system. Product protection is therefore an area of research to enable CH₄activation, especially in the area of process optimization and catalyst design. Of particular interest are designing catalysts to reduce benzene oxidation and further limit CH₃OH diffusion pathways. The successful product protection process described herein meets several factors: the catalysts are designed to minimize the gaseous lifetime of CH₃OH; scavenging reaction reactants and products are resistant to complete oxidation and do not interfere with partial methane oxidation to methanol; complete CH₄oxidation does not occur over the catalyst designed to scavenge methanol; and the rate of the scavenging reaction is greater than the rate of methanol formation so that the scavenging reaction is not rate-limiting. This example provides a pathway towards achieving industrially relevant product selectivities at desirable CH₄conversions.

EXAMPLE 2

The following example describe the synthesis and characterization of the first catalyst and the second catalyst.
Cu-SSZ-13 was synthesized in a one-pot method via the use of tetraethylenepentamine (TEPA). Copper sulfate pentahydrate (98% trace metals basis, Sigma-Aldrich) was first dissolved in water followed by the addition of TEPA (technical grade, Sigma-Aldrich) and stirred for 1 hour before the addition of N,N,N-trimethyl-1-adamantanamine hydroxide solution (TMAdaOH, 25 wt. % in H₂O, Sachem). Following, aluminum hydroxide (Al(OH)₃, 80.3 wt. %, SPI Pharma 0250) was dissolved in the solution before fumed silica (Sigma-Aldrich, 99.8%) was added. The final composition of the mixture was 1 SiO₂: 0.07 Al(OH)₃:0.4 TMAdaOH: 44 H₂O: 0.01 CuSO₄: 0.011 TEPA. The solution was stirred at room temperature for 2 hours, transferred to four 23-mL Teflon-lined stainless steel autoclaves (No. 4749, Parr Instruments) and subjected to hydrothermal treatment at 433 K for 5 days in an oven under autogenous pressure and rotation (60 rpm). After hydrothermal treatment, the product was separated from the mother liquor by centrifugation, washed several times with distilled H₂O until pH <9 and dried overnight at 393 K. The zeolite was calcined under dry air (Dry Size 300, Airgas) with the following temperature profile: heat 1 K min⁻¹to 423 K and hold for 1 hour at 423 K, heat 1 K min⁻¹to 623 K and hold for 1 hour at 623 K, and lastly heat 1 K min⁻¹to 853 K and hold for 10 hours.
H-MFI was synthesized according to the following procedure: To 41.343 g water, 6.663 g tetrapropylammonium hydroxide (TPAOH, 40 wt% in water, SACHEM) was added and stirred for 15 minutes. Following, 0.135 g aluminum hydroxide (SPI Pharma 250) was added followed by 2.25 g sodium hydroxide solution in water (NaOH, Sigma-Aldrich, 23.0 wt. % in water). The mixture was stirred for at least 10 minutes. Then, 2.604 a fumed silica (Cab-o-Sil M5) was slowly added and shaken vigorously. The final gel composition was 1 SiO₂: 0.04 Al(OH)₃:0.3 TPAOH: 0.3 NaOH. The gel was allowed to homogenize and age with stirring for 16 hours before being transferred to 23-mL mL Teflon-lined stainless steel autoclaves (No. 4749, Parr instruments) and subjected to hydrothermal treatment under static conditions at 453 K for 2 days in an oven under autogenous pressure. After hydrothermal treatment, the product was separated from the mother liquor by centrifugation, washed several times with distilled H₂O until pH<9 and dried overnight at 393 K. The zeolite was calcined under dry air (Dry Air Size 300, Airgas) with the following temperature profile: heat 1 K min⁻¹to 423 K and hold for 1 hour at 423 K, heat 1 K. min⁻¹to 623 K and hold for 1 hour at 623 K, and lastly heat 1 K min⁻¹to 853 K and hold for 10 hours.
Following calcination, to remove Na, 1 g of zeolite was stirred in 60 mL of a 1.0 M solution of ammonium nitrate (≥99%, Sigma-Aldrich) for 16 hours at room temperature. The suspension was filtered at room temperature, rinsed with 300 mL of deionized. H₂O, and the recovered zeolite was immediately subjected to the same ion exchange twice more under the same conditions. Following, the zeolite was dried overnight at 393 K in stagnant air and calcined following the same profile described above.
The first catalyst and the second catalyst were characterized using elemental analysis. Copper, sodium, and aluminum contents were determined using inductively coupled plasma atomic emission spectroscopy (ICP-AES, Agilent 5100) or inductively coupled plasma mass spectrometry (ICP-MS, Agilent 7900). 5-10 mg of zeolite were placed in a polyethylene microfuge tube (1.5 mL) and digested in 20 microliters of hydrofluoric acid (48 wt. %, trace metals basis, Sigma-Aldrich) for 2 hours. The hydrofluoric acid solution was diluted to a total mass of 10.0 g using 2 wt. % aqueous nitric acid (HNO₃) (veritas purity, GFS Chemicals). When using ICP-MS, 1 mL of these solutions were diluted once more to 10 mL solution total. A six-point calibration curve was built using ICP standard solutions of 1,000 ppm Cu in 2 wt. % HNO₃1,000 ppm Al in 2 wt. % HNO₃and 1,000 ppm Na in 2 wt. % HNO_3.All standard solutions were purchased from Sigma-Aldrich (TraceCERT).
The molar ratios of Si/Al_totand Cu/Al_totin the catalysts were calculated as follows: The unit cell of a zeolite, is given by:
H_x ⁺Na_y ⁺Cu_z ²⁺(AlO₂)_n ^−(SiO ₂)_m(H₂O) _k
where subscripts refer to the molar ratios of each component within the unit cell of a zeolite. Local charge balance was assumed to occur within the zeolite, requiring x=n−2−y.
From the unit cell given above, the mass balance of the unit cell is given by the following equation on a per gram zeolite basis:
$\begin{matrix} 1 = a \frac{{g SiO}_{2}}{g zeolite} + b \frac{{g [{AlO}_{2}]}^{-}}{g zeolite} + c \frac{{g Cu}^{2 +}}{g zeolite} + d \frac{g {Na}^{+}}{g zeolite} + e \frac{g H^{+}}{g zeolite} + f \frac{g H_{2} O}{g zeolite} \end{matrix}$
where each coefficient represents the weight percent of each species. The weight percent of Al, Cu and Na were directly calculated using ICP-AES, allowing b, c, and d to be determined. Converting the weight percentages of Al, Cu and Na to mole percentages per grain zeolite, e was then calculated using the local charge balance of cations on the zeolite framework. The weight percentage of H₂O (f) was assumed to be equal to the weight percentage of H₂O in the zeolite framework unit cell (2-7 wt %). The mass balance was then solved for the weight percentage of SiO₂(a).
Si/Al_totwas calculated by
$\frac{Si}{{Al}_{tot}} = \frac{a}{b} \frac{m_{{AlO}_{2}}}{m_{{SiO}_{2}}} \times \frac{1 mol Si}{1 mol {SiO}_{2}} \times \frac{1 mol {AlO}_{2}}{1 mol Al}$
where m_iis the molar mass of element i.
Cu/Al_totwas calculated by
$\frac{Cu}{{Al}_{tot}} = \frac{c}{b} \frac{m_{{AlO}_{2}}}{m_{Cu}} \times \frac{1 mol {AlO}_{2}}{1 mol Al}$
The crystal structures of zeolite catalysts were determined from powder x-ray diffraction patterns collected using a Bruker D8 diffractometer using Cu-Kα, radiation (λ=1.5418 Å, 40 kV, 40 mA). Data were recorded in the range of 3-40 20 with an angular step size of 0.02° and a rate of 4° min⁻¹.
Scanning electron microscopy was performed on a Zeiss Merlin High-resolution SEM. Samples were crushed into a fine powder and loaded on to carbon black tape. Micrographs were collected at 3.0 kV, 100 pA, and 6.7 mm WD with the HE-SE2 detector in High Resolution column mode.

EXAMPLE 3

The following example describes the experimental apparatus used for the partial oxidation of a reactant and the coupling reaction of the intermediate resulting from the partial oxidation with a co-reagent.
Reactions were conducted in a continuous, tubular flow reactor (304 stainless steel tube, O.D. 0.25 in, I.D. 0.18). The reactor tube was mounted inside a single-zone furnace (850W/115V, Applied Test Systems Series 3210). Temperature was controlled using a thermocouple (Omega, model TJ36-CASS-116U) mounted slightly downstream of the catalyst, bed connected to a temperature controller (Digi-Sense model 68900-10). The mixture of a copper-exchanged zeolite and a proton-form zeolite were mixed in a ratio of 1:3 by weight, ground with a mortar and pestle, and then vortexed to ensure a homogeneous catalyst mixture. 0.35 g of this zeolite mixture (pelletized and sieved into 250-420 micrometer particles) were packed between quartz wool plugs and rested on the thermocouple in the middle of the furnace heating zone. Control reactions were performed with the same absolute loadings of the individual catalysts and catalyst beds were pelletized to the same size distribution. Void volume above and below the catalyst bed was filled with borosilicate glass beads to reduce homogeneous combustion. Blank reactors were loaded in the same manner in the absence of catalyst. For testing with increased catalyst loading a 304 stainless steel, O.D. 0.5 in, I.D. 0.40 in. reactor was used.
The flow of gases, including He (ultra-high purity, Airgas), 1% O₂in He (ultra-high purity, Airgas), and CH₄(research grade, Airgas) were controlled with independent mass flow controllers (Brooks instruments LLC). H₂O (typically 3.2 kPa, the saturation vapor pressure at 298 K) was introduced into the gas stream via a stainless steel saturator and benzene was introduced using a syringe pump (Harvard Apparatus) with a heated liquid injection port. System pressure was controlled with a back pressure regulator
(Equilibar U3L Series) between the reactor and the gas chromatograph. Stainless steel gas transfer lines were heated with resistive heating tape from the point of liquid injection until the gas chromatographic analysis unit. Typical reaction pretreatment involved calcining the catalyst at 823 K for 8 hours under 50 mL min⁻¹dry air.
CH₃OH, dimethyl ether (DME), CO, CO_2,benzene, toluene, and xylene partial pressures evolved during catalytic tandem oxidation and alkylation reactions were quantified using a gas chromatograph (Agilent Technologies, 7890B). The gas chromatograph was equipped with a mechanizer, flame ionization detector, and thermal conductivity detector. Three columns were used for product separation: two HP-PLOT Q PT (30 m×0.53 mm×40 μm, Agilent #19095P-QO4PT) and HP PLOT Molsieve (30 m×0.53 mm×50 μm, Agilent #19095P-MS0E).
Reported values for selectivity and rates of product formation were averaged over three data points upon reaching steady-state.
Calibration curves for CO₂, CH₃OH, CO, and DME were constructed by flowing known mixtures of 1% CO₂/He, 0.5% CH₃OH/He, 90 ppm CO/N₂or 10% DME/He and He, respectively, to a gas chromatograph. Calibration curves for benzene and toluene were constructed by injecting known liquid flow rates into a flowing gas stream of known flow rate. A response factor for xylene was inferred from that of toluene by carbon weighting.
The large partial pressure of CH₄in the gas stream during catalytic CH₄oxidation reactions prevented the accurate quantification of CH₄consumption. As such, CH₄conversion was assumed to be equal to the total molar flow rate of carbon of all observed.
products divided by the initial molar flow rate of CH₄:
$X_{C H 4} = \frac{\sum_{i = 1}^{N} C_{i} F_{i}}{F_{CH 4, 0}}$
where X_CH4is the conversion of CH_4,F_iis the molar flow rate of product i, C_iis the number of carbon atoms incorporated from CH₄into product i, ΣC_iF_iis the total molar flow rate of carbon of all products, and F_CH4.0is the initial molar flow rate of CH₄.
Product selectivity for catalytic CH₄oxidation and tandem oxidation and alkylation was defined as:
$S_{i} = \frac{C_{i} F_{i}}{\sum_{i = 1}^{N} C_{i} F_{i}}$
where S_iis the selectivity of product i on a C-atom basis, C_iis the number of carbon atoms incorporated from CH₄into product i, F_iis the molar flow rate of product i, and ΣC_iF_iis the total molar flow rate of carbon of all products.
Product yield for catalytic CH₄oxidation and tandem oxidation and alkylation was defined as:
$Y_{i} = \frac{C_{i} F_{i}}{N_{C u} or g_{cat}}$
where Y_iis the selectivity of product i on a C-atom basis, N_Cuis the numberof moles of Cu within the zeolite determined by ICP, and g_catis the catalyst loading.

EXAMPLE 4

The following example describes a ¹³C₆H₆isotope switching experiment.
To quantify the contribution of benzene oxidation to the observed rates of CO and CO₂formation, a ¹³C₆H₆(Sigma Aldrich, 423637, 99 atom %) isotope switching experiment was completed. Prior to the experiment, the catalyst bed was calcined under 50 sccm dry air at 823 K for 8 hours before cooling to 543 K. At 543 K and 1 bar, reactant flows were introduced with unlabeled benzene until steady-state was attained.
Steady state was tracked by gas chromatography and an online mass spectrometer (Hiden Analytical HPR-20/QIC). CO (mlz=28), ^—CO (m/z=29), CO₂(m/z=44), ¹³CO₂(m/z =45), benzene (m/z=78), and ¹³C₆benzene (m/z=84) were tracked by mass spectrometry. Upon reaching steady-state, the benzene feed was switched to ¹³C₆H₆until a steady-state was reached. The feed was then switched back to unlabeled benzene. The catalyst bed was then heated to 603 K and the same experiment was repeated. The rates of CO and CO₂formation were unchanged with the change in benzene isotope. The change in the mass spectrum signal of each species was assumed to respond linearly to the gas phase concentration of each species. The natural abundance of ¹³CO and ¹³CO₂were accounted for in accounting for the contribution of benzene oxidation to the rates of CO and CO₂ formation as follows:
Prior to isotope switch:
$x = \frac{^{12} CO signal}{^{13} CO Signal}$ $Rate of^{13} CO formation pre - switch = \frac{Total Rate of CO Formation}{1 + x}$
Following isotope switch:
$y = \frac{^{12} CO signal}{^{13} CO Signal}$ $Rate of^{13} CO formation post - switch = \frac{Total Rate of CO Formation}{1 + y}$ $Rate of CO formation from benzene = Rate of^{13} CO formation post - switch - Rate of^{13} CO formation pre - switch$ $Fractional Contribution of Benzene = \frac{Rate of CO formation from benzene}{Rate of^{12} CO formation pre - switch}$
Table 2 summarizes the contributions of benzene oxidation to the rates of CO and CO₂formation and FIGS. 17A-18B present the MS signals.

TABLE 2

Percent contributions of CH₄and C₆H₆to observed rates of formation
of CO and CO₂at 543 and 603 K under tandem oxidation and alkylation
reactions. (0.366 g Cu-CHA-2 + 1.097 g H-MFI-3), flow conditions: 78.3
sccm, P_CH4= 17.8 kPa, P_C6H6= 0.80 kPa, P_O2= 0.09 kPa,
P_H2O= 3.1 kPa, bal He, atmospheric pressure.

Temperature (K)	Source	CO	CO	₂

543	CH ₄	15%	81%
	C₆H₆	85%	19%
603	CH ₄	15%	58%
	C₆H₆	85%	42%

EXAMPLE 5

The following example describes an estimation of benzene oxidation across conditions.
Based on the observed rates of CO and CO₂formation stemming from benzene at 543 and 603 K, 1 bar, estimates of the contribution of benzene oxidation to CO and CO₂formation rates were obtained by using kinetic dependences and estimates of apparent activation energies, Estimates of apparent activation energies for CO and CO₂formation from benzene were obtained from FIG. 4B. The apparent activation energy for CO was 45 kJ/mol and for CO₂was 79 kJ/mol. It was demonstrated that the rate of CO₂, formation was independent of P_benzeneand the dependence of CO₂formation from benzene on P_O2is 0.4 order, as shown in FIG. 16. These dependences were assumed to hold for CO. These dependences along with the apparent activation energies allows for estimation of benzene oxidation rates across temperature and pressure. For FIG. 16, the catalyst composition and feed mixture was (0.2625 g Cu-CHA-1+0.7875 g H-MFI-1), 74.5 sccm, 543 K. P_O2=0.1 kPa, Pbenzene=0.80 kPa, P_H2O=3.1 kPa, bal He.
While several embodiments of the present invention have been described and illustrated herein, those of ordinary skill in the art will readily envision a variety of other means and/or structures for performing the functions and/or obtaining the results and/or one or more of the advantages described herein, and each of such variations and/or modifications is deemed to be within the scope of the present invention. More generally, those skilled in the art will readily appreciate that all parameters, dimensions, materials, and configurations described herein are meant to be exemplary and that the actual parameters, dimensions, materials, and/or configurations will depend upon the specific application or applications for which the teachings of the present invention is/are used. Those skilled in the art will recognize, or be able to ascertain using no more than routine experimentation, many equivalents to the specific embodiments of the invention described herein. It is, therefore, to be understood that the foregoing embodiments are presented by way of example only and that, within the scope of the appended claims and equivalents thereto, the invention may be practiced otherwise than as specifically described and claimed. The present invention is directed to each individual feature, system, article, material, and/or method described herein, In addition, any combination of two or more such features, systems, articles, materials, arid/or methods, if such features, systems, articles, materials, and/or methods are not mutually inconsistent, is included within the scope of the present invention.
The indefinite articles “a” and “an,” as used herein in the specification and in the claims, unless clearly indicated to the contrary, should be understood to mean “at least one.”
The phrase “and/or,” as used herein in the specification and in the claims, should be understood to mean “either or both” of the elements so conjoined, i.e., elements that are conjunctively present in some cases and disjunctively present in other cases. Other elements may optionally be present other than the elements specifically identified by the “and/or” clause, whether related or unrelated to those elements specifically identified unless clearly indicated to the contrary. Thus, as a non-limiting example, a reference to “A and/or B,” when used in conjunction with open-ended language such as “comprising” can refer, in one embodiment, to A without B (optionally including elements other than B); in another embodiment, to B without A (optionally including elements other than A); in yet another embodiment, to both A and B (optionally including other elements); etc.
As used herein in the specification and in the claims, “or” should be understood to have the same meaning as “and/or” as defined above. For example, when separating items in a list, “or” or “and/or” shall be interpreted as being inclusive, i.e., the inclusion of at least one, but also including more than one, of a number or list of elements, and, optionally, additional unlisted items. Only terms clearly indicated to the contrary, such as “only one of” or “exactly one of,” or, when used in the claims, “consisting of,” will refer to the inclusion of exactly one element of a number or list of elements. In general, the term “or” as used herein shall only be interpreted as indicating exclusive alternatives (i.e. “one or the other but not both”) when preceded by terms of exclusivity, such as “either,” “one of,” “only one of,” or “exactly one of.” “Consisting essentially of,” when used in the claims, shall have its ordinary meaning as used in the field of patent law. As used herein in the specification and in the claims, the phrase “at least one,” in reference to a list of one or more elements, should be understood to mean at least one element selected from any one or more of the elements in the list of elements, but not necessarily including at least one of each and every element specifically listed within the list of elements and not excluding any combinations of elements in the list of elements. This definition also allows that elements may optionally be present other than the elements specifically identified within the list of elements to which the phrase “at least one” refers, whether related or unrelated to those elements specifically identified, Thus, as a non-limiting example, “at least one of A and B” (or, equivalently, “at least one of A or B,” or, equivalently “at least one of A and/or B”) can refer, in one embodiment, to at least one, optionally including more than one, A, with no B present (and optionally including elements other than B); in another embodiment, to at least one, optionally including more than one, B, with no A present (and optionally including elements other than A); in yet another embodiment, to at least one, optionally including more than one, A, and at least one, optionally including more than one, B (and optionally including other elements); etc.
In the claims, as well as in the specification above, all transitional phrases such as “comprising,” “including,” “carrying,” “haying,” “containing,” “involving,” “holding,” and the like are to be understood to be open-ended, i.e., to mean including but not limited to. Only the transitional phrases “consisting of” and “consisting essentially of” shall be closed or semi-closed transitional phrases, respectively, as set forth in the United States Patent Office Manual of Patent Examining Procedures, Section 2111.03.

Claims

1. A composition, comprising:

a first catalyst comprising a Cu-modified zeolite; and

a second catalyst capable of a coupling reaction between (a) an intermediate resulting from a reaction of a reactant at the first catalyst, and (b) a co-reagent, wherein a rate of diffusion of the co-reagent within one or more cages and/or pores of the first catalyst is lower than a rate of diffusion of the intermediate within the one or more cages and/or pores of the first catalyst.

2. The composition of claim 1, wherein the rate of diffusion of the co-reagent within the one or more cages and/or pores of the first catalyst is no more than 60%, 50%, 40%, or 30% the rate diffusion of the intermediate within the one or more cages and/or pores of the first catalyst.

3. The composition of claim 1, wherein the rate of diffusion of the co-reagent within the one more cages and/or pores of the first catalyst is no more than 20% the rate diffusion of the intermediate within the one or more cages and/or pores of the first catalyst.

4. The composition of claim 1, wherein the rate of diffusion of the co-reagent within the one or more cages and/or pores of the first catalyst is no more than 10% or 5% the rate diffusion of the intermediate within the one or more cages and/or pores of the first catalyst.

5. The composition of claim 1, wherein the rate of diffusion of the co-reagent within the one or more cages and/or pores of the first catalyst is no more than 1% the rate diffusion of the intermediate within the one or more cages and/or pores of the first catalyst.

6. A composition, comprising:

a first catalyst comprising a Cu-modified zeolite; and

a second catalyst capable of a coupling reaction, wherein the coupling reaction is alkylation and/or etherification.

7. The composition of claim 1, wherein the first catalyst comprises Cu-modified SSZ-13, AEI, AFX, MAZ, and/or mixtures thereof.

8. The composition of claim 1, wherein the first catalyst comprises Cu-modified SSZ-13.

9. The composition of claim 1, wherein the second catalyst comprises a solid acid catalyst.

10. The composition of claim 1, wherein the second catalyst comprises a zeolite, a metal oxide, a metal-organic-framework (MOF), a polyoxometallate, sulfated zirconia, and/or mixtures thereof.

11. The composition of claim 10, wherein the metal oxide comprises alumina and/or silica.

12. The composition of claim 10, wherein the metal oxide comprises molybdenum oxide and/or tungsten oxide.

13. The composition of claim 12, wherein the metal oxide is supported by aluminosilicate.

14. The composition of claim 1, wherein the second catalyst comprises ZSM-5, ZSM-22, NU-87, SSZ-33, beta, and/or mixtures thereof.

15. The composition of claim 14, wherein the second catalyst comprises ZSM-5.

16. A method, comprising:

exposing a reactant to a first catalyst comprising a Cu-modified zeolite, thereby oxidizing the reactant to provide an intermediate; and

exposing the intermediate and a co-reagent to a second catalyst, thereby reacting the co-reagent with the intermediate to provide a product.

17. The method of claim 16, wherein the reactant comprises methane, ethane, propane, butane, and/or mixtures thereof.

18. The method of claim 16, wherein the first catalyst comprises Cu-modified SSZ-13, AEI, AFX, MAZ, and/or mixtures thereof.

19. (canceled)

20. The method of claim 16, wherein the intermediate comprises methanol, ethanol, propanol, butanol, and/or mixtures thereof.

21. The method of claim 16, wherein the co-reagent comprises an aromatic, an alcohol, an alkene, and/or mixtures thereof.

22.-40. (canceled)

41. A composition, comprising:

a first catalyst comprising a Cu-modified zeolite; and

a second catalyst capable of a coupling reaction between (a) an intermediate resulting from a reaction of a reactant at the first catalyst, and (b) a co-reagent, wherein a rate of diffusion of the co-reagent relative to the first catalyst is lower than a rate of diffusion of the intermediate relative to the first catalyst.

42. (canceled)