OA20839A - Catalyst structure and method of upgrading hydrocarbons in the presence of the catalyst structure - Google Patents

Abstract

A catalyst structure includes a porous support structure, where the support stucture includes an aliuninosilicate materia. Any two or more metals are loaded in the porous support structure, the two or more metals selected from the group consisting of Ga. Ag, Mo, Zn. Co and Ce, where each metal loaded in the porous support structure is present in an amount from about 0.1 wt% to about 20 wt%. In example embodiments, the catalyst structure includes three or more of the metals loaded in the porous support structure. The catalyst structure is used in a hydrocarbon upgrading process that is conducted in the presence of methane, nitrogen or hydrogen

Description

CATALYST STRUCTURE AND METHOD OF UPGRADING HYDROCARBONS IN THE PRESENCE OF THE CATALYST STRUCTURE

CROSS-REFERENCE TO RELATED APPLICATION

This application daims priority from U.S. Provisional Patent Application Serial No. 62/807,795, filed February 20, 2019, the disclosure of which is incorporated herein by reference in îts entirety.

FIELD

The présent invention is directed toward the formulation of a heterogeneous catalyst and a process of utilizing the catalyst in the upgrading of hydrocarbons in a mixed gas environment for improving the quality of such hydrocarbons while also producing aromatic hydrocarbons.

BACKGROUND

Demand for hydrogen will increase in the upcoming years as a resuit of stricter environmental législation relating to the processîng of hydrocarbons, including petroleum, naturel gas, coal, bitumen, refined products, and bio-oils. Not only législation but more extensive Processing of residues and higher diesel demand compared with petrol will also increase hydrogen's demand.

There are varions hydrotreating processes associated with upgrading and refining of hydrocarbons, including: upgrading and hydrocracking (long-chain hydrocarbons are cracked to shorter chains); hydrodesulphurization (sulphur compounds are hydrogenated to hydrogen sulphide H₂S); hydroisomerisation (normal paraffins are converted into îso-paraffins to improve the product propertîes, e.g. RON); and dearomatisation (aromatics are hydrogenated to cyclo paraffins or alkanes).

Hydrogen volumes that are consumed increasingly exceed those produced in a platformer and hâve to be supplemented by other sources, ail of which produce significant amounts of CO₂. Some examples of processes for hydrogen on-site supply include steam reforming of methane or other hydrocarbons, recovery from refinery off-gases, recovery from syngas, and gasification of oil refining residues.

Significant effort has been applied to provîding a suitable and energy efficient process for upgrading hydrocarbons by conversion of saturated components în the hydrocarbons to more valuable Chemicals. For example, the upgrading of a heavy oil in volves the breaking or cracking of large hydrocarbon molécules withîn the heavy oil into smaller molécules under certain conditions. In particular, bitumen derived feedstock heavy oil can be upgraded by cracking the larger hydrocarbon molécules into smaller, more désirable compounds such as benzenes, toluènes and xylcnes (BTX) components. During the cracking/reaction process, undesired feedstock molécules (e.g., aspiraitene contents) are converted to more volatile and other désirable molécules in addition to BTX components, such as octane and other gasoline or petroleum products as well as siinpler (e.g., mono) aromatic compounds. Certain atoms, such as sulfur and nitrogen, can also be removed to improve the quality of the final oil product.

A conventional approach to upgrade hydrocarbons is a thermal cracking process, which produces the desired components along with an undesirable amount of coke and COj. Thermal cracking is typically foliowed with hydrotreating of the cracked components using hydrogen gas, typically obtained by an energy intensive process of steam reforming of natural gas (thus increasing the cost of the hydrotreating process). Another conventional process for upgrading heavy oil is by treating with H2 gas in the presence of a heterogenous catalyst to achieve catalytic hydrocracking of the heavier hydrocarbons. Hydrotreating catalysts typically include high surface area supports such as AI2O3 typically doped with nickel, molybdenum, and noble group metals such as platinum (Pt) and rhénium (Re). Such hydrotreating steps are costly and inefficient due to the high température (e.g., about 800 °C or greater) and high pressure (e.g., about - 100 - 200 atm) operating conditions required to achieve satisfactory levels of upgrading (e.g., viscosity réduction and hydrogen incorporation).

In vîew of the foregoing, it would be advantageous to provide a process that is more energy efficient, environmentally efficient, reduces GHG (greenhouse gas) émissions, and less expensive for processing hydrocarbons to produce a desired final product.

BRIEF SUMMARY

In accordance with embodiments described herein, a catalyst structure comprises a porous support structure comprising an alummum oxide material (e.g,, AbOj), an aluminosilicate material, or a zirconium oxide material (e.g.. ZrO₂), and any two or more metals loaded in the porous support structure, the two or more metals selecled from the group consisting ol’Ga, Ag, Mo, Zn, Co and Ce. Each métal is loaded in the porous support structure is présent in an amount from about 0.1 wt% to about 20 wt%.

In other embodiments, a process of fonning the catalyst structure is provided. Further, a method of upgrading hydrocarbons in the presence of the catalyst structure is described herein.

The above and still further features and advantages of the présent invention will become apparent upon considération of the following detail ed description of spécifie embodiments thereof.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 depicts a réaction System for upgrading heavy oïl utilizing a catalyst structure and in a methane, N₂ or H₂ environment in accordance with example embodiments described herein.

Like référencé numerals hâve been used to identify like éléments throughout this disclosure.

DETAILED DESCRIPTION

In the following detailed description, while aspects of the disclosure are disclosed, altemate embodiments of the présent disclosure and their équivalents may be devised without parting from the spirît or scope of the présent disclosure. It should be noted that any discussion herein regarding “one embodiment”, “an embodiment”, “an exemplary embodiment”, and the like indicate that the embodiment described may include a particular feature, structure, or characteristic, and that such particular feature, structure, or characteristic may not necessarily be included in every embodiment. In addition, référencés to the foregoing do not necessarily comprise a référencé to the saine embodiment. Finally, irrespective of whether it is explicitly described, one of ordînary skill in the art would readily appreciate that each of the particular features, structures, or characteristics of the given embodiments may be uîilized in connection or combination with those of any other embodiment discussed herein.

Varions operations may be described as multiple discrète actions or operations in tum, in a manner that is most helpiùl in understanding the claimed subject matter. However, the order of description shoukl not be construed as to impi y that these operations are necessarily order dépendent. In parlicular, these operations may not be performed in the order of présentation. Operations described may be performed in a different order than the described embodiment. Varions additional operations may be performed and/or described operations may be omitted in additional embodiments.

For the purposes of the présent disclosure, the phrase “A and/or B” means (A), (B), or (A and B). For the purposes of the présent disclosure, the phrase “A, B, and/or C” means (A), (B), (C), (A and B), (A and C), (B and C), or (A, B and C).

The tenus “comprising,” “including,” “having,” and the like, as used with respect to embodiments of the présent disclosure, are synonymous.

In accordance with example embodiments, catalyst structures are described herein for use in combination with processes for upgrading a first hydrocarbon product utilizing methane and one or more of such catalyst structures to achieve a hîgher quality product including smaller, more désirable molécules (e.g., BTX components) as well as other desired physical properties for the final or second, upgraded hydrocarbon product (e.g., a desired viscosity, a desired total acid number or density, etc.).

The use of methane, rather than hydrogen alone, in the hydrocarbon upgrading process obviâtes the need for a hydrotreating step at high pressures and températures. Instead, the hydrocarbon can be converted to aromatic or paraffinic products via a multi-step mechanism consisting of cracking, oligomérization, cyclization and hydrogen transfer steps. However, the design of the catalyst so as to activate methane and the hydrocarbon substrate and selectively form desired products is very important to the efficacy of hydrocarbon, upgrading. The catalyst structures described herein facilitate the upgrading of hydrocarbons in the presence of methane and at much lower températures and pressures than those typically required when utilizing a hydrotreating process. For example, methane can be converted at lower températures (e.g., in the range of 300-600 °C) and at lower pressures (e.g., about 1-200 atm, such as about 1-50 atm) when combined with hydrocarbon molécules in the presence of a catalyst structure as described herein.

Types of hydrocarbons for upgrading

As used herein, the term “hydrocarbon” or “hydrocarbon product” refers to any type of hydrocarbon material in a solid, semi-solid (e.g., slurry or gel like State) and/or liquid that can be processed as described herein to from a final, upgraded product having one or more désirable properties and/or characleristics for a particular use or purpose. In other words, a first hydrocarbon product (e.g., a raw or intermediate processed hydrdocarbon product) is subjected to an upgrading process as described herein to obtain a second (final) hydrocarbon product having one or more enhanced properties and/or characteristics.

Types of hydrocarbon products that can be subjected to upgrading include, wîthout limitation the following:

- Crude oil, which can be categorized as follows:

— light crude oil (or light oil) - crude oil having an API gravîty of 31.1° API or hîgher. The light crude oils generally hâve a dynamîc viscosity less than 2 x 10³ cP (mPa*s).

Types of light crude oils can be further categorized into very light oils including, wîthout limitation, jet fuel, diesel fuel, gasoline, kerosene, petroleum ether, petroleum spirit, and petroleum naphtha.

- medium crude oil (or medium oil) - crude oil having an API gravîty ranging between 22,3° API and 31.1° API. Medium crude oils typically hâve a higher viscosity in relation to light crade oils, the dynamîc viscosity is often within the range of 2 x 10' 2 x 10⁴ cP (mPa-s).

— heavy crude oil (or heavy oil) - crade oil having an API gravîty ranging between 10° API and 22.2° API, Heavy crade oils typically hâve a higher viscosity in relation to medium crade oils. In particular, a heavy crude oil can hâve a dynamîc viscosity of at least about 1 x 10⁵ cP (mPa s). Heavy crade oil also includes extra heavy oil or bitumen. For example, bitumen (which can be obtained, e.g., in Alberta, Canada) often has an average density of 1.0077 g/cm³, an API gravîty of S.9° API, and a dynamîc viscosity of 2 x 10⁴- 2 χ 10⁶ cP (mPa-s) at atmospheric conditions. Other types of heavy oil include bunker fuel and residual oil or resid (i.e., fuel oil remaining after removal of certain distillâtes, such as gasoline, from petroleum).

— Synthetic fuel oils, including, wîthout limitation:

-- synthetic oils created using a Fischer-Tropsch (F-T) process.

- bio oils (or pyrolysis oils) created from biomass (e.g-, wood, algae, etc.) and utilizing a pyrolysis process.

In addition, hydrocarbon products can also be categorized based upon further properties, such as whether or not the hydrocarbon product has been sweetened. For example, a hydrocarbon product (e.g., heavy. medium or light oil) can be sweetened (containing su 1 fur in an amount less than 0.42% by volume) or unsweetened or sour (containing sulfur in an amount greater than 0,50%).

The upgrading process of the hydrocarbon products results in a change in one or more properties in the hydrocarbon products. The change (from fïrst hydrocarbon product to upgraded, second hydrocarbon product) to one or more properties in the hydcrocarbon product include, without limitation, change (decrease) in density, change (decrease) in viscosity, change (decrease) in sulfur content, change (decrease) in TAN (total acid number), change (decrease) in an amount (e.g., weight percentage) of olefins, change (decrease) in an amount (e.g., weight percentage) of nitrogen, change (decrease) in pour point, change (increase) in an amount (e.g·, weight percentage) of one or more aromatic hydrocarbons, change (increase) in the hydrogen to carbon ratio (H/C ratio), and change (increase) in cetane number.

Catalvst structures

In accordance with the présent invention, a catalyst structure is provided that comprises an acîdîc mono or multi-metallic (e.g., bimetallic), highly porous structure for converting or upgrading hydrocarbons in a methane environment. It is noted that the catalyst structures described herein can also be used to upgrade heavy oil in a H₂ or N₂ environment, although utilizing a methane gas environment is preferred. In further embodiments, a feed including methane combined with N₂ and/or H₂ can be provided for the hydrocarbon upgrading process. The upgraded oil product has a lower viscosity in relation to the heavy oil, a lower density in relation to the heavy oil, a decrease in total acid number (TAN) in relation to the heavy oil, and an increase in content of lighter hydrocarbons such as aromatics and paraffïns in relation to the heavy oil.

The catalyst structure can be synthesized by impregnating or doping a suitable support material with two or more metals (e.g., utilizing process such as wet imprégnation or ion exchange to adsorb métal ions to the porous surfaces of the support material), A suitably porous support material can be an aluminum oxide material (e.g., AI2O3), an ahiminosilicate (zeolite) material, or a zirconium oxide material (e.g., ZrO₂). Some non-limiting examples of a suitable zeolite material for use as a support material for the catalyst structure include a ZSM-5 type zeolite (e.g., HZSM-5 zeolite, NaZSM-5 zeolite, etc.), A-type zeolite, 1,-type zeolite, HY type zeolite and a zeolite structure commercially available from Rive Technology (Monmouth Junction, New Jersey). An ammonium type zeolite can also be utilized by conversion to a hydrogen type zeolite (e.g., by calcination in static air at a température of about 400-600 °C for a period of about 4-6 hours). When utilizîng a zeolite material as the support material, a SiO₂ to AEO3 ratio of the zeolite support material can be in the range of 1-280 (i.e., a ratio of SiO₂ to Ai₂Oj that is 1 : I to 280 : 1), such as a range of 5-28, or a range of 23-280. The zeolite material can further hâve a BET surface area in the range from 350 m7g and 950 m /g. The support materials can optionally be modified with phosphores prior to being synthesized into a suitable catalyst structure.

Suitable metals that can be used to dope the porous support material include any one or more (and preferably any two or more) of gallium (Ga), silver (Ag), zinc (Zn), molybdenum (Mo), cobalt (Co) and cérium (Ce). Each métal dopant or the combination of métal dopants can be provided within the catalyst structure (e.g., in métal or métal oxide form) in an amount ranging from 0.1-20 wt%. For certain metals, such as Ag and Ga, the preferred métal loading is from 0.2 - 2 wt%. For other metals, such as Co, the preferred métal loading is 0.3 - 3 wt%. Spécifie examples are provided herein of different métal loadings for catalyst structures. It is noted that the term weight percentage (wt%) of a métal within a catalyst structure, as described herein, refers to the mass of a particular métal element divided by the mass of the catalyst support (i.e., the mass of the porous catalyst support material prior to métal loading) and then multiplied by 100 (to obtain a percentage value).

The porous support material can be doped with a suitable amount of one or more metals in the following manner. One or more métal salts can be dissolved in deionized water to form an aqueous solution of one or more métal precursors at suitable concentration(s) within solution. Métal precursor salts that can be used to form the catalyst structure include, wîthout limitation, chlorides, nitrates and sulfates. The one or more métal precursors in solution are then loaded into the porous support material to achieve a desired amount of metals within the catalyst structure (e.g., from 0.1 20 wt%). Any suitable loading process can be perfonned to load metals within the porous support material. Some non-limiting examples of métal loading processes include: IWI (incipient wetness imprégnation, where an active métal precursor is first dissolved in an aqueous or organic solution, the metal-containing solution is then added to a catalyst support containing the same pore volume as the added solution volume, where capillary action draws the solution into the pores); WI (wet imprégnation, where more liquid than the IW1 volume is added to the support, and the solvent is then removed by évaporation); 1E (ion-exchange, where métal cations are exchanged into the support from solution); and FI (Framework incorporation, where mêlais are added to the support materials during the synthesis step of the support),

Depending upon the particular loading process, the résultant meta! loaded catalyst structure can be dried at a température between about 80 °C to about 120 ’C for a period of time between about 2 hours to about 24 hours. The dried catalyst structure can then be subjected to calcination under air, N? or another gas or réduction under H? at a température ranging from about 300 - 700 °C and at a suitable ramped or stepped increased heating rate (e,g., heating rate increases the température at about 5-20 °C/min), where such calcination températures, times and heating rates can be modified depending upon the type or types of metals doped into the catalyst structure as well as reaction conditions associated with use ofthe catalyst structure.

The résultant métal doped catalyst structure is suitable for use in hydrocarbon upgrading under a methane (or H? or N2) environment in processes as described herein. The catalyst structure can be processed into a granular form having a granule size as desired for a particular operation. Some examples of granular sizes include a diameter (or cross-sectional dimension) range that is 1 5 mm, and a lengthwise or longitudinal dimension range that is 5 - 10 mm. The catalyst structure can also be formed into any other suitable configuration.

For example, the catalyst structure can also be converted into pellets, e.g., by combining the powder into pellets using a suitable binder material. For example, the catalyst structure in powder form can be mixed with colloïdal silica, methyl cellulose and a solution of an acid such as acetic acid or citric acid, where the mixture can then be extruded to form pellets. The weight ratios between catalyst powder and colloïdal silica, between catalyst powder and methyl cellulose, and between catalyst powder and acetic acid or citric acid solution can range from 1:0.5-2, 1:0.05-0.2 and 1:0.1-0.5, respectively. The mass concentration of acetic acid or citric acid solution can be about 10-50 wt. %. Some non-lîmiting examples of colloïdal silica used to form the pellets include LUDOX® AM-30 and LUDOX® HS-40. In formïng the pellets, the components can be added into 8 the catalysl powder in the foilowing order: methyl cellulose, acetic or citrîc acid solution and colloïdal silica. In a first step, the pellet is prepared by well mixing (e.g., using a suitable mixer) of the catalyst powder and methyl cellulose The acetic or citric acid solution is prepared and then combined with the catalyst mixture and the contents well mixed, followed next by the addition of colloïdal silica and then further mixing. Next, the combined mixture is extruded using a suitable extrader at about room température (e.g., about 20-25 °C). To control the shape and size of catalyst pellets, the extrader is equipped with a suitable fonning die. In example embodiments, a catalysl pellet can hâve a cylindrical shape that is about 0.5-3 mm in length and/or diameter. After extrusion, the catalyst pellet can be dried at about 80-100 °C for about 8-12 hours, followed by calcination at 550 °C for about 12 hours (e.g., utilizing a heating rate that încreases température in an amount ranging from about about 5-20 °C/min).

The catalyst structure in a powder form can be utilized, e.g., in a batch reactor System, while the catalyst structure in a pelleted form can be utilized in a continuous flow System. Catalyst structures as described herein can further be used for heavy od upgradîng in a number of different types of reactor Systems including, without limitation, batch reactor Systems, continuous tubular reactors (CTR), continuous stirred-tank reactors (CSTR), semi batch reactors, varying catalytic reactors such as fixed bed, trickle-bed, movîng bed, rotating bed, fluidîzed bed, slurry reactors, a non-thermal plasma reactor, and any combinations thereof.

In addition, the catalyst structure can be regenerated, either before or after a period of time of its use in upgrading hydrocarbons, to enhanced the performance of the catalyst structure. The régénération process comprises rinsing the catalyst with toluene, drying in air to remove toluene (e.g., drying at 100-200°C, e.g., about 150 °C, for at least 1 hour, e.g., about 3 hours or greater) and calcination (heating in air) at a température of at least about 500 °C (e.g., about 600 °C or greater) for a sufficient period of time, e.g., at least about 3 hours (e.g., about 5 hours or greater). The régénération process can also be repeated any number of times and depending upon a particular application. For a catalyst structure that has been used to upgrade hydrocarbons, the régénération process (e.g,. single régénération, twice régénération, etc.) can be used to regenerate or refresh the catalyst structure such that its performance in upgrading hydrocarbons is enhanced in relation to the performance of the catalyst structure prior to the régénération process. In particular, the performance of the catalytic reaction for the catalyst structure can improve when subjected to a régénération process and after the catalyst structure has been used in long-term industrial applications. While not bound by any particular theory, it would appear that the active catalytîc sites in the catalysts are further activated during the régénération process. In particular, the métal oxides may be converted to sulfides during the reaction and bcllcr disperse in the catalyst structure. In the régénération process, métal migration may take place to achieve a better dispersion, resulting in improved catalytic performance. The improved catalytic performance upon régénération of the catalysts described herein rend ers these catalysts highly suitable for commercial applications in the upgrading of oil (or other hydrocarbon) feedstocks in a methane (or H? or N?) environment. Further, the régénération process can be repeated a plurality of times (e.g., regenerated twice, regenerated three times, etc.) for a particular application to enhance the catalytic performance of the catalyst structure.

Some examples of forming catalyst structures in accordance with the présent invention are now described in the following examples.

EXAMPLE 1

A 1 wt.%Ag-l wt.%Ga/HZSM-5(23:l) catalyst structure was prepared in the following manner. An ammonium type ZSM-5 (NH4-ZSM-5, SiC^AhOj moiar ratio of 23:1) support structure in powder form and commercially available from Zeolyst USA was calcined in statîc air at 600 °C for 3 hours. The following métal salts were disseIved in deionized water to form a métal precursor solution: 0.13g AgNOj and 0.30g Ga(NO₃)₃-9H₂O (where the mass of water used to préparé the solution is about the same as the mass of the support structure), The HZSM-5 support was impregnated with the métal precursor to achieve a suitable métal weîght loading. The obtaîned wet powder was first dried in an oven at 92 °C overnight, followed by calcination at 550 °C in static air.

The catalyst powder was then converted to a pellet form as follows. The catalyst power was mixed with methyl cellulose, colloïdal silica and the citric acid solution according to the following procedures: ïwt.%Ag-lwt.%Ga/HZSM-5 (23:1) catalyst was first mixed with methyl cellulose in a mass ratio of catalyst: methyl cellulose of 1:0.1; next, a citric acid solution is added in a mass ratio of catalyst: citric acid solution = 1:0.3, where the mass concentration of citric acid solution was 20 wt. %; next, colloïdal silica (LUDOX® AM-30) was also added as the binder in a mass ratio of 1:1. After ail components were added and suîtably mixed, the extrusion was conducted with an extruder 10 at room température. After extrusion, the wet catalyst pellets were dried at 80 °C overnight (e.g., about 8-12 hours), followed by calcination at 550 °C for 12 hours.

The 1 wt.%Ag-l wt.%Ga/HZSM-5(23:1) catalyst structure pellets were regenerated twice before being tested in a hydrocarbon upgrading process. Each régénération process is carried out by rinsing the catalyst with toluene. drying in air to remove toluene at 150 °C for 3 hours and calcination (heating in air) at 600 °C for 5 hours.

A heavy oil feedstock sample with a viscosity of 1.12 ^x 10⁵ mPa^s at 15.6 °C was used as the feedstock for the test. The catalyst pellets were loaded in a continuous flow reactor. The reaction was carried out continuously over a period of about 1 week and under 10.0 MPa in methane and at 410 °C, where the flow rate of feedstock was set so that the weight hour space velocity (WHSV) was 1 h'¹. During the process, use of the catalyst structure resulted in a réduction in viscosity of the processed oil sample to 325 mPas, where a 106.3 wt.% mass liquid yield was achieved after reaction. The liquid yield was determîned as foliows:

Weight of collected liquid product Liquid yield = . -----------—--------— X 100%

Weight of consumed heavy crude

The coke formation rate is calculated by following équation:

The weight of coke.on catalyst „ , _J. (The decreased weight after calcination) _d nnn?

Coke formation rate = —---™— ------„ ——_:---------_:— x 100%

The weight of catalyst after calcination x Réaction time

Asphaltene content in the feedstock was reduced from 13.21 wt.% to 5.23wt.%, resulting in greatly increased light end products (as set forth in Table 1 below). Good stability of the oil product was also witnessed after the reaction, where the Peptization value or P-value of the product oil was 2.42 (indicatîng that the product oil îs stable enough for pipeline transportation as well as the downstream refmery).

EXAMPLE 2

A lwt.%Ag-iwt.%Ga-5wt.%Mo-10wt.%Ce/HZSM-5(23:l) catalyst was prepared in the following manner. A NH4-ZSM-5 (SiCbiAkOj molar ratio of 23:1) support structure in powder form and obtained from Zeolyst USA was calcined in static air at 600 °C for 3 hours. The following métal salts were dissolved in deionized water to form a métal precursor solution: Ce^ChhtolHhO, 11 (ΝΗ₄)6Μο₇Ο₂4·4Η₂Ο, Ga(NO₂)3'9H₂O and AgNOj. The HZSM-5 support was impregnated with the métal precursor solution to achieve a suitable métal weight loading. The obtained wet powder was first dried in an oven at 92 °C ovemight, followed b y calcination at 550 °C in static air.

The catalyst powder was then converted to a pellet fonn as follows. The catalyst power was 5 mixed with methyl cellulose, colloïdal silica and the citric acid solution according to the following procedures: the lwt.%Ag-lwt.?^/ôGa-5wt.%Mo-10wt.%Ce/HZSM-5(23:l) catalyst was first mixed with methyl cellulose in a mass ratio of catalyst: methyl cellulose of 1:0.15; next, a citric acid solution is added in a mass ratio of catalyst: citric acid solution = 1:0.2, where the mass concentration of citric acid solution was 30 wt. %; next, colloïdal silica (LUDOX® HS-40) was also 10 added as the binder in a mass ratio of 1:1. After ail components were added and suitably mixed, the extrusion was conducted with an extrader at room température. After extrusion, the wet catalyst pellets were dried at 95 °C ovemight (e.g., about 8-12 hours), followed by calcination at 550 °C for 12 hours.

The iwt.%Ag-lwt.%Ga-5wt.%Mo-10wt.%Ce/HZSM-5(23:l) catalyst structure pellets were 15 regenerated twice before being tested in a hydrocarbon upgrading process. Each régénération process was carried ont by rinsîng the catalyst with toluene, drying in air to remove toluene at 150 °C for 3 hours and calcination (heating in air) at 600 °C for 5 hours.

A heavy oil (bitumen) sample with a viscosity of 641 mPa-s at 15.6 °C was used as the feedstock to test the catalyst structure. The reaction was carried out under 5.0 MP a and 400 ^ÛC in a 20 methane environment. The weight hour space velocity was 1 h¹. The product oil had a reduced viscosity of 340 cP, and 95.2 wt.% mass liquid yield was achieved. A significant amount of the resin and asphaltene contents in the feedstock were converted to light ends and aromatics in the product oil (see Table 1 below). The total acid number or TAN value was also reduced from 1.40 mg KOH/g in the bitumen feedstock to 0.31 mg KOH/g in the product oil. Good stability was also witnessed 25 after the reaction,

SARA tests (measuring amounts of saturâtes, asphaltenes, resins, and aromatics in the oil product) were conducted for the oil products obtained in Examples 1 and 2 and utilizing the catalyst structures prepared in those tests. The test results are provided in Table 1 :

Table 1 : SARA Test Results for Product Oil of Examples 1 and 2

	Example 1	Example 2
SARA	Feedstock	Oil Product	Feedstock	Oil Product
Components	(wt%)	(wt%)	(wt%)	(wt%)
Light End	2.93	20.57	6.1	16.3
Saturâtes	22.32	20.28	18.6	19.6
Aromatics	39.89	33.03	30.2	38.4
Res ins	19.50	19.74	28.2	19.0
Asphaltenes	13.21	5.23	16.9	6.7

Other catalyst structures with different combinations of métal dopants and/or different catalyst supports can also be formed in accordance with the présent invention, where the method of forming such catalyst structures can be the same or similar to that described herein. Example 3 5 provides a further example of a catalyst structure.

EXAMPLE 3

A catalyst structure with the formula of l%Ag-l%Ga-2%Co-6%Mo-I0%Ce/HZSM-5(23:l) was prepared in the following manner. A NH₄-ZSM-5 (SiO₂:Al₂O₃ molar ratio of 23:1) support structure in powder fonn and obtained from Zeolyst USA was calcined în static air at 600 °C for 3 hours. The following métal salts were dissolved in deionized water to form a métal precursor solution: Ce(NO₃)₃'6H₂O_f (ΝΗ₄)6Μο₇Ο₂4·4Η₂Ο, Co(NO₃)₂-6H₂O, Ga(NO₃)₃-9H₂O and AgNO₃. The mass of water used to préparé each precursor solution equals to the mass of the ZSM-5 support. The HZSM-5 support was impregnated with the métal precursor solution to achieve a suitable métal weight loading. The obtained wet powder was first drîcd in an oven at 92 °C ovemight, followed by calcination at 550 °C in static air.

A sériés of experiments were performed to evaluate the réaction performance of different catalysts formed according to methods as described herein, where the catalysts were utilîzed in a process to upgrade different feedstocks of heavy oil (or other hydrocarbon product) under different conditions. Table 2 provides a list of varions catalysts formed in accordance with the methods described herein, inciuding a listing of operating température and pressure conditions in a reactor that included the catalyst, and the final (oil product) viscosity and liquid yield of a lieavy oil subjected to upgrading în the presence of methane and the particular catalyst in the reactor.

Table 2: Performance of Catalyst Structures

Catalyst Number	Catalyst	Temp (“C)	Pressure (MPa)	Viscosity of Oil Product (mPas)	Liquid yield (%)
1	lwt.%Ag-lwt.%Ga/HZSM-5(23:l)	400	6	6374	92.4
2	lwt.%Ag-lwt.%Ga/HZSM-5(23:l)	400	10	9232	104.1
3	lwt.%Ag-lwt.%Ga/HZSM-5(23:l)	420	8	37	89.4
4	lwt.%Ag-lwt.%Ga/HZSM-5(23:1), regenerated	400	5	473	106.1
5	lwt.%Ag-lwt.%Ga/HZSM-5(23:l), regenerated twice	400	5	286	108.6
6	lwt.%Ag-lwt.%Ga-5wt.%Mo- 10wt.%Ce/HZSM-5(23:1)	400	5	985	92.6
7	lwt.%Ag-lwt.%Ga-5wt.%Mo10wt.%Ce/HZSM-5(23:1), regenerated	400	5	205	108.8
8	lwt.%Ag-lwt.%Ga/HZSM-5(23:l), regenerated twice	410	10	179	102.9
9	lwt.%Ag-lwt.%Ga/HZSM-5(23:l), regenerated twice	420	10	42	99.9
10	1 wt.%Ag-1 wt.%Ga-2wt.%Co- 6wt.%Mo-10wt.%Ce/HZSM-5(23:l)	400	3	177	97
11	1 wt.%Ag-l wt.%Ga-5wl.%Mo10wt.%Ce/HZSM-5(23:l)	400	3	274	98
12	1 wt.%Ag-l wt.%Ga-5wt.%Mo10wt.%Ce/HZSM-5(23:l), sulfide	400	3	164	98
13	1 wt.%Ag-1 wt.%Ga-2wt.%Co6wt.%Mo-10wt.%Ce /HZSM5(23:1)	400	3	174	98
14	lwt.%Ag-lwt.%Ga-2wt.Co6wt.%Mo-10wt.%Ce /HZSM5(23:1)	400	3	488	99
15	1 wt.%Ag-1 wt.%Ga-2wt. %Co- 6wt.%Mo-10wt.%Ce/HZSM- 5(23:1), sulfide	400	3	143	98
16	1 wt.%Ag-l wt.%Ga/Zeolite A (1:1)	400	3	103	97.2
17	lwt.%Ag-lwt.%Ga/ZSM-5(280:l)	400	3	67	94.7

18	1 wt.%Ag-1 wt.%Ga-5wt.%Mo- 10wt.%Ce/HZSM-5(23:I)	500	0.1	3	48.8
19	1 wt.%Ag-1 wt.%Ga-5wt.%Mo- 10wt.%Ce/HZSM-5(23:l)	300	10	118	95.8
20	1 wt.%Ag-1 wt.%Ga-5wt.%Mo10wt.%Ce/HZSM-5(23:l)	400	3	1198	98.9
21	1 wt%Ag-1 wt.%Ga-5wt.%Mo10wt.%Ce/HZSM-5(23:l)	400	3	959	95.2
22	1 wt.%Ag-1 wt.%Ga-5wt.%Mo10wt.%Ce/HZSM-5(23:l)	400	3	3927	96.2
23	1 wt.%Ag-1 wt.%Ga-5wt.%Mo10wt.%Ce/HZSM-5(23:1)	400	3	694	99.9
24	1 wt%Ag-1 wt.%Ga-5wt.%Mo10wt.%Ce/HZSM-5(23:1)	400	3	25.6	100.2
25	1 wt.%Ag-1 wt.%Ga-5wt.%Mo10wt.%Ce/HZSM-5(23:1)	400	3	98	99.0
26	lwt.%Ag-lwt.%Ga-5wt.%Mo10wt.%Ce/HZSM-5(23:1 )	400	3	10	90.1
27	Iwt.%Ag-lwt.%Ga-5wt.%Mo- 10wt.%Ce/HZSM-5(23:l)	420	5	119	103.0
28	1 wt.%Ag-1 wt.%Ga-5wt.%Mo10wt.%Ce/HZSM-5(23:l)	420	10	42	100.0

The reactions for the catalysts in Table 2 variée! as follows. For Catalysts 1-9, the experimental reactions were performed in a continuons flow reactor having a liquid hour space velocity (LHSV) of I h'¹ and the gas phase was CH4. The reaction processes were similar to the 5 processes described herein in Exampies 4 and 5. For Catalysts 1-3, the heavy oil sample had a viscosity of 1.12 x 10⁵ mPa s at 15.6 °C; for Catalysts 4-7, the heavy oil sample had a viscosity of 641 mPa-s at 15.6 °C; for Catalysts 8 and 9, a heavy oil sample had a viscosity of 1911 mPa^s at 15.6 °C. The LHSV was 1 h’¹ and the gas phase was CH4 for the reactions associated with Catalysts 1-9.

For Catalysts 10-15, the experimental réactions were performed in a 300 mL batch reactor, and the mass ratio between the heavy oil feedstock and the catalyst was 100:1. In a typical reaction, 60 grams of heavy oil feedstock with certain amount of catalyst (e.g., 1 wt.%) was loaded into a Parr batch reactor of 300 mL capacity. The cylinder was pressurized with H₂, CH4, CjHg or their mixtures after the air inside the reactor was purged out. The autoclave was then quickly heated up 15 to 400 ^UC (i.e. reaction température) and kept at the reaction température for 20-60 minutes while stirring. When the upgrading was to be terminated, the autoclave body was plunged into a cold water bath and the température could be lowered below 300 °C in less than 2 minutes. After being cooled to room température, the gas was removed from the reactor before the liquid products were collected and analyzed.

The heavy oïl feedstock for Catalyst 10 had a viscosity of 1.10 x 10’mPa-s at 15.6 °C. The heavy oil feedstock for Catalysts 11-15 had a viscosity of 2249 mPa-s at 15.6 °C. For Catalysts ΙΟΙ 3, the reactor was charged with 1.5 bar CjHjj and then filled with 30 bar CH4and heated to 400 °C, where it was then hekl for 40 min with continuous stirring. For Catalysts 14 and 15, the reactor was filled with 30 bar H₂ and heated to 400 ^UC, where it was then held for 40 min with continuous 10 stirring.

From the experimental tests performed with the catalysts as described herein, it can be seen that the performance of certain catalysts at variable life stages are different. In particular, the regenerated catalysts listed in Table 2 (Catalysts 4, 5, 7, 8 and 9) were determined to perfonn better than those from the original catalysts in terms of reduced product viscosity and increased liquid 15 yield. As previously noted herein, this phenomenon shows that the performance of the catalytic reaction would improve after a régénération process in long-term industrial applications.

Thus, the heterogeneous catalyst structures formed in accordance with the methods described herein facîlitate upgrading of a hydrocarbon product (e.g., a heavy oil such as bîtumen) in a methane (or N₂ or H₂) environment, yielding a product oil with a reduced viscosity as well as lighter 20 hydrocarbons (as determined, e.g., by SARA analysis). The activated methane species participate in hydrocarbon upgrading to improve the quality and incorporate into the product molécules. A good catalytic performance in the heavy oil upgrading is also obtained under N₂ or H₂ environment. The employment of a heterogenous catalyst structure facilitâtes this upgrading process under milder and therefore more economical reaction conditions (e.g., lower températures and pressures).

Furthermore, control over product seiectivity is achieved through catalyst design, further increasing the commercial value of cracked distillâtes. Support materials with variable structure, morphoiogy, acidity and porosity provide tunable catalytic performance of the catalysts when loaded with métal promoters to further increase catalyst effectiveness.

Systems and methods for upgrading hydrocarbons utilizing the catalyst structures

The conversion of oil feedstocks and selectivity toward fonning smaller hydrocarbon products such as aromatics and paraffins can be fine-tuned using catalyst structures as described herein and under methane, N₂ or H₂ environments. Different reactor Systems and modified operating conditions (e.g., températures and pressures) as well as implémentation of the catalyst structures within the reactor Systems can also be implemented to achieve a varied level of upgrading of a first hydrocarbon product to form a second, upgraded hydrocarbon product (e.g., a lighter hydrocarbon product).

Methane is particularly useful for upgrading of heavy oil in the presence of catalysts described herein. Whîle typically regarded as chemically inert due to its stable structure, methane activation has been a challenge in naturel gas utilization. However, it has been determined that methane conversion can be significantly enhanced in the presence of higher hydrocarbon reactants (such as those in hydrocarbons, including paraffins, olefins and aromatics) and at lower températures,

After reaction of a first hydrocarbon product in a reaction System such as depicted in FIG. 1, and using methane and one or more catalyst structures as described herein, the qualîty of the hydrocarbons is upgraded such that the upgraded second hydrocarbon product emerging from the reaction system is improved based upon a change (from first hydrocarbon product to upgraded, second hydrocarbon product) in one or more properties including, without limitation, change (decrease) in density, change (decrease) in viscosity, change (decrease) in sulfur content, change (decrease) in TAN (total acid number), change (decrease) in an amount (e.g., weight percentage) of olefins, change (decrease) in an amount (e.g., weight percentage) of nitrogen, change (decrease) in pour point, change (increase) in an amount (e.g., weight percentage) of one or more aromatic hydrocarbons, change (increase) in the hydrogen to carbon ratio (H/C ratio), and change (increase) in cetane number. While methane is shown in FIG. 1 as the input gas that is combined with the heavy oil feedstock, in other embodiments the input gas could be any one of combination of methane, nitrogen and/or hydrogen.

For example, when upgrading a crude oil (e.g., a heavy oil) using a process with a catalyst structure as described herein, a change in properties between first and second (upgraded) hydrocarbon products is achîeved in terms of a decrease in viscosity, a decrease in density, a decrease in total acid number (TAN), a decrease in large or heavier hydrocarbons (e.g., decrease in asphaltenes), a decrease in content or concentration of heterogeneous atoms (e.g., S and N) and an increase in content or concentration of paraffins and light aromatics including BTX. After a reaction, the viscosity can be reduced to 100-500 cP from above 1 χ 10⁵ cP, while the density can be reduced by 0.2-0.5 g/mL. The percentage of light hydrocarbons with a boiling point below 220 °C in the second hydrocarbon product can be increased by 5-30%.

An example reaction System for upgrading a hydrocarbon product utilizing methods as described herein is schematically depîcted in FIG. 1. Refemng to FIG. 1, a hydrocarbon feedstock line 10 (e.g., bitumen or other heavy oil) is directed along with a llow line 20 of methane (or, alternatively, or Nj) to an inlet of a reactor 30 that is opérâted at a suitable température and pressure range. For example, operating températures during the upgrading process and within the reactor can be controlled so as to range from about 200-500 °C, such as from about 300-500 °C, or from about 300-450 °C. Operating pressures within the reactor can range from about 1-200 atm, or from about 1-50 atm.

A variety of different heavy oil feedstocks can also be upgraded utilizing catalyst structures and methods as described herein, where the feedstocks can hâve viscosîties of 1 x 10⁵ mPas or greater at 15.6 °C. Varions types of reaction Systems can also be utilized, such as high pressure and high température batch reactor Systems, continuons stirred-tank reactors (CSTRs), continuous tubular reactors (CTRs), semi batch reactors, non-thermal plasma reactors, and varying catalytîc reactors (e.g., fixed bed, trickle-bed, moving bed, rotating bed, fluidized bed, as well as slurry reactors). Reactant hydrocarbon feedstock to catalyst mass ratios can be between 200:1 to 1:10 in a batch reactor System, and the heavy oil feedstock can hâve a liquid hourly space velocity (LHSV) and/or a weight hourly space velocity (WHSV) of about 0.1-100 h¹, e.g., about 0.1-10 h'¹, in a flow reactor System. The gas flow (e.g., methane, H2, or N2) in a flow reactor System can also be se so as to hâve a gas hourly space velocity (GHSV) in the range of about 0.1-100 h'¹, e.g., about 0.1-10 h'¹.

In the example embodiment of FIG. 1, the reaction system includes a fixed catalyst bed reactor 30. The system further includes a separator 40, an oil pump (not shown) to deliver the heavy raw oil from a crude oil tank to the reactor 30, a product tank (not shown) for storing the upgraded oil product, and a cooling system 50 to cool the products emerging from the reactor. The raw oil can be preheated to 80 °C in the crade oil tank. The preheated crade oil feedstock line 10 is mixed with the high pressure methane provided from line 20 (methane at room température and 10 MPa) before entering into the reactor 30. With the presence of the catalyst structure within the iîxed bed reactor 30, methane will be further activated and react with the crude oil within the reactor. The choice of a particular catalyst structure can also improve the selectivity of lighl hydrocarbon products formed within the reactor. The partially upgraded oil can flow oui from the bottom of the reactor 30. then enter imo the séparation unit 40. In the séparation unit 40, gas-liquid séparation can occur. The cooling system 50 can comprise a water cooling heat exchanger al room température and atmospheric pressure (or any other suitable fluid heat exchanger) that cools the upgraded oil (e.g., to achieve a hîgher liquid yield). After the séparation process, the emerging liquid oil product exits via a lower outlet 60 in the separator 40 and is collected in the product tank, while the gas emerges from a separate outlet 70 of the separator 40 and is subject to post processing. The hydrocarbons including methane can optionally be recycled back to the reactor 30 after the removal of sulfur containîng compounds.

The upgrading process as described herein further minimize the génération of CO₃ in the process. In particular, upgrading processes utilizing the catalyst structures as described herein in which a first hydrocarbon product is provided as a feedstock to yield a second hydrocarbon product (having one or more different properties from the first hydrocarbon product as described herein) can resuit in the génération or production of CO₂ that is less than 5% by weight of the second hydrocarbon product, in some scénarios less than 4% by weîght of the second hydrocarbon product, or less than 3% by weight of the second hydrocarbon product, or less than 2% by weîght of the second hydrocarbon product, or even less than 1% by weight of the second hydrocarbon product (e.g., substantîally no CO? is formed in the process).

Some examples of upgrading a heavy crude oil (also referred to as a raw oil) using a catalyst structure as described herein and the System of FIG. 1 are now described.

EXAMPLE 4

A lwt.%Ag-lwt%Ga/zeolite A(l:l) catalyst was prepared in the following manner. A zeolite A (SiCfoALOj molar ratio of 1:1) support structure in powder form was obtained from Zeolyst USA. The zeolite was extruded into pellet form with the following recipe: catalyst: colloïdal silica: methyl cellulose: acetic acid solution=l:0.5:0.2:0.1. After ail components were added and suitably mixed, the extrusion was conducted with an extrader at room température. After extrusion, the wet catalyst pellets were dried at 95 °C ovemight (e.g., about 8-12 hours), followed by calcination at 300 °C for 12 hours.

The foilowîng métal salts were dissolved in deionized water to form a métal precursor solution: Ga(NOriy9H2O and AgNOj. The shaped zeolite A support in pellet form was impregnated with the métal precursor solution to achieve a suitable métal weight loading. The obtained wet powder was first dried in an oven at 80 °C ovemight, followed by calcination at 300 °C in static air with a ramp rate of 5 °C/min.

A heavy oil sample with a viscosîty of 2488 mPa'S at 15.6 °C was used as the feedstock to test the catalyst performance in a batch reactor. The reaction was camed out under 3.0 MPa and 400 °C in a methane environment. The weight ratio of oil to catalyst was 100:1. The product oil had a reduced viscosity of 103 niPa s, and 97.2 wt.% mass liquid yield was achieved. A notable réduction of density from 0.96455 g/cm³ to 0.95526 g/cm³ was observed, indicating that a significant amount of heavy fraction was converted to light fraction during the upgrading process.

EXAMPLE 5

A 1 wt%Ag-l wt.%Ga/ZSM-5(280:1) catalyst was prepared in the foilowîng manner. A NH4ZSM-5 (SiChiALCh molar ratio of 280:1) support structure in powder form obtained from Zeolyst USA was calcined in static aîr at 600 °C for 3 hours. The zeolite was extruded into pellet form with the foilowîng recipe: catalyst: colloïdal silica: colloïdal silica: methyl cellulose: citric acid solution = 1:2:0.2:0.1. After ail components were added and suitably mixed, the extiusion was conducted with an extrader at room température. After extrusion, the wet catalyst pellets were dried at 95 °C ovemight (e.g., about 8-12 hours), followed by calcination at 700 °C for 12 hours.

The foilowîng métal salts were dissolved in deionized water to form a métal precursor solution: GafNCDvOHiO and AgNOj. The shaped zeolite A support in pellet form was impregnated with the métal precursor solution to achieve a suitable métal weight loading. The obtained wet powder was first dried in an oven at 120 °C ovemight, followed by calcination at 700 °C in static air with a ramp rate of 20 °C/min.

A heavy oil sample with a viscosity of 2488 mPa-s at 15.6 °C was used as the feedstock to test the catalyst performance in a batch reactor. The reaction was camed out under 3.0 MPa and 400 °C in a methane environment. The weight ratio of oil to catalyst was 100:1. The product oil had a 20 reduced viscosity of 67 mPa s, and 94.7 wt.% mass liquid yield was achieved. A significant réduction of density from 0.96455 g/cm³ to 0.94130 g/cm³ was observed, indicating that a significant amount ofheavy fraction was converted to light fraction during the upgrading process.

EXAMPLE 6

A lwt.%Ag-lwt.%Ga-5wt.%Mo-10wt.%Ce/HZSM-5(23:l) catalyst was prepared in the following manner. A NH₄-ZSM-5 (SiO^rALOj molar ratio of 23:1 ) support structure in powder form and obtained from Zeolyst USA was calcined in static air at 600 C for 3 hours. The following métal salts were dîssolved in deionized water to form a métal precursor solution: CetNOjjs^ôHiO, (ΝΗ₄)₆Μθ7θ24·4Η2θ, Ga(NO3)3'9H₂O and AgNOs. The HZSM-5 support was impregnated with the 10 métal precursor solution to achîeve a suitable métal weight loading. The obtained wet powder was first dried in an oven at 92 °C ovemight, followed by calcination at 550 °C in static air.

A heavy oil sample with a viscosity of 2488 mPa-s at 15.6 °C was used as the feedstock to test the catalyst performance in a batch reactor. The reaction was carried out under 1 atm and 500 °C în a methane environment. The weight ratio of oil to catalyst was 200:1. The product oil had a 15 reduced viscosity of 3 mPa-s, and 48.8 wt.% mass liquid yield was achieved, indicating that the content of light fraction was increased dramatically during the upgrading process.

EXAMPLE 7

A lwt.%Ag-lwt.%Ga-5wt.%Mo-10wt.%Ce/HZSM-5(23:l) catalyst was prepared in the same manner as described in Example 6.

A heavy oil sample with a viscosity of 2488 mPas at 15.6 °C was used as the feedstock to test the catalyst performance in a batch reactor. The reaction was carried out under 100 atm and 300 °C in a methane environment. The weight ratio of oil to catalyst was 1:10. The product oil had a reduced viscosity of 118 mPa-s, and 95.8 wt.% mass liquid yield was achieved, indicating that the content of light fraction was increased dramatically during the upgrading process.

EXAMPLE 8

A 1 wt.%Ag-lwt.%Ga-5wt.%Mo- 10wt.%Ce/HZSM-5(23:1) catalyst was prepared in the same manner as described in Example 6.

A heavy oil sample with a viscosity of 2488 mPas al 15.6 °C was used as the ieedstock to test the catalyst performance in a fixed bed reactor. The reaction was carried out under 30 atm and 400 “C in a methane environment. The LHSV was set to be 100 h’L The product oil had a reduced viscosity of 1 198 mPa-s, and 98.9 wt.% mass liquid yield was achieved, indicating that the content of light fraction was increased to a certain degree during the upgrading process.

EXAMPLE 9

A lwt.%Ag-lwt.%Ga-5wt.%Mo~10wt.%Ce/HZSM-5(23:l) catalyst was prepared in the same manner as described in Exemple 6.

A high sulfur content diesel sample with a sulfur content of 2306 ppm was used as the feedstock to test the catalyst performance in a fixed bed reactor. The reaction was carried out under 30 atm and 400 °C in a methane environment. The LE1SV was set to be 2 h'¹. The product oil had a reduced sulfur content of 959 ppm, and 95.2 wt.% mass liquid yield was achieved. The 60% decrease of sulfur content indicated that most of the sulfur species in the original diesel sample was removed after the upgrading process.

EXAMPLE 10

A lwt.%Ag-lwt.%Ga-5wt.%Mo-10wt.%Ce/HZSM-5(23:l) catalyst was prepared in the same manner as described in Example 6.

A vacuum residue sample with a viscosity of 660,000 mPa s at 30 °C (> Ι,Οθθ,Οθθ at 15.6 °C) was used as the feedstock to test the catalyst performance in a batch reactor. The reaction was carried out under 30 atm and 400 °C in a methane environment. The weight ratio of oil to catalyst was 100:1. After the reaction, 96.2 wt.% mass liquid yield was achieved. It is worth noting that the viscosity was reduced dramatically to 3,927 mPa s, indicating the upgrading process is highly effective for viscosity réduction of heavy oil samples. The lightening effect of this process was also confirmed by the decrease of density from 0.9742 g/cm³ (vacuum resuide) to 0.9533 g/cm^J (product).

EXAMPLE 11

A lwt.%Ag-lwt.%Ga-5wt.%Mo-10wt.%Ce/HZSM-5(23:l) catalyst was prepared in the same manner as described in Example 6.

A marine diesel oil sample with a sulfur content of S27 ppm was used as die feedstock to test the catalyst performance in a batch reactor. The réaction was carried out under 30 alm and 400 C in a methane environment. The weight ratio of oîl to catalyst was 100:1. The product oil had a reduced sulfur content of 694 ppm, and 99.9 wt.% mass liquid yield was achieved. It is suggested that the sulfur content was reduced to a certain degree during the upgrading process. The effect was also coniîrmed b y the decrease of density from 0.8535 g/cm³ (marine diesel oil) to 0.8519 g/cm^J (product).

EXAMPLE 12

A 1 wt.%Ag-l wt.%Ga-5wt.%Mo-10wt.%Ce/HZSM-5(23:1) catalyst was prepared in the same manner as described in Exampie 6.

A diluted bitumen sample with a viscosity of 39.1 mPa s at 15.6 °C was used as the feedstock to test the catalyst performance in a batch reactor. The reaction was carried out under 30 atm and 400 °C in a methane environment. The weight ratio of oil to catalyst was 100:1. The product oil had a reduced viscosity of 25.6 mPa s, and 100.2 wt.% mass liquid yield was achieved. Besides, the density of oil sample also got reduced from 0.8590 to 0.8536 g/cm³. It can be seen that the heavy fractions in diluted heavy oil sample can also be effect successfully converted to light fractions during the upgrading process.

EX AMPLE 13

A lwt.%Ag-Iwt.%Ga-5wt.%Mo-10wt.%Ce/HZSM-5(23:l) catalyst was prepared in the same manner as described in Example 6.

A bunker fuel sample with a viscosity of 18,900 mPa s at 15.6 °C and a sulfur content of 14,597 ppm was used as the feedstock to test the catalyst performance in a batch reactor. The reaction was carried out under 30 atm and 400 °C in a methane environment. The weight ratio of oil to catalyst was 100:1. The product oil had a reduced viscosity of 98 mPa'S, and 99.0 wt.% mass liquid yield was achieved. Besides, the sulfur content in product was dramatically reduced to 3,638 ppm. Besides, the density of oil sample was reduced from 0.97745 to 0.95802 g/cm³. It is confirmed that the aforementioned catalytic upgrading process is capable of signîfîcantly reducing the sulfur content as well as converting heavy fractions into light fractions simultaneously, which is highly favorable for the utilization of bunker fuel resources.

EXAMPLE 14

A lwt.%Ag-lwt.%Ga-5wt.%Mo-10wt.%Ce/HZSM-5(23:l) catalyst was prepared in the same manner as described in Example 6.

A jet fuel sample was used as the feedstock to test the catalyst perforai a nce in a tîxed bcd reactor. Lhe reaction was canied ont under 30 atm and 400 °C in a methane environment, The LHSV was set to be 2 h'¹. The distribution of different types of species in feed and product oil is listed in Table 3, It is apparent thaï the aromatic content increased dramatically after the reaction, especially marked by the notable increase of BTEX content from 2,74 wt% to 26.83 wt%. It is highly promising since the generated products are greatly economically valuable.

Table 3: Distribution of different types of species in feed and product sample for Ex ample 14

	Paraffin	Naphthene	Olefin	Aromatic	Benzene	Toluene	Ethylbenzene	Xylene
Feed	53.19	14.92	1.05	30.84	0	0	0	2.74
Product	21.11	15.82	1.61	61.45	2.35	9.13	2.73	12.62

EXAMPLE 15

A raw oil is preheated to 70 °C in the crude oil tank. The preheated crude oil flow is mixed with the high pressure methane before entering into the reactor of the reaction System. The fixed bed reactor is loaded with lwt.%Ag-lwt.%Ga/HZSM-5 (23:1) catalyst structure (e.g., a catalyst structure formed in the same or similar process as described in Example I), The reactor is charged to about 50 atm CH4 and heated to about 420 °C. The liquid flow of crude oil has a liquid hourly space velocity (LHSV) of about I h'¹ and gas flow has gas hourly space velocity (GHSV) of about 12 h¹. The heavy oil reacts with methane in the presence of the catalyst structure in the reactor. After the reaction is complété (with a résidence time of 3—15 minutes), the partially upgraded oil flows out from the bottom of the reactor, and then enters the séparation unit. In the séparation unit, gas-liquid séparation occurs. The water cooling System is control led to decrease the température of the séparation unît to about room température. After séparation, the liquid flows to the product tank and collected, while die separated gas flows to the post processing System. Aller upgrading under methane and utilizing the catalyst structure, the viscosity of heavy oil is reduced from 6,774 mPa s to 119 mPas, and a mass liquid yield of 103% is achieved.

EXAMPLE 16

A raw oil is preheated to 70 °C in the cru de oil tank. The prehealcd crude oil flow is mixed with the high pressure CH₄ before entering into the reactor ofthe reaction System. The fixed bed reactor is loaded wilh 1 wt.%Ag-lwt.%Ga/HZSM-5 (23:1) catalyst structure (e.g., a catalyst structure formed in the same or similar process as described in Example 1). The reactor is charged to about 100 atm CH₄ and heated to about 420 °C. The liquid flow of crude oîl has a liquid hourly space velocity (LHSV) of about 0.5 h’¹ and gas flow has gas hourly space velocity (GHSV) of about 20 h’¹. The heavy oil reacts with methane in the reactor. After the réaction is complété (with a résidence time of 3 - 15 minutes), the partially upgraded oil flows out from the bottom of the reactor, and then enters the séparation unit. In the séparation unit, gas-liquid séparation occurs. The water cooling System is controlled to decrease the température of the séparation unît to about room température. After séparation, the liquid flows to the product tank and collected, while the separated gas flows to the post processing System. After upgrading under methane and utilizing the catalyst structure, the viscosity of heavy oil is reduced from about 1,911 mPa s to about 42 mPa s. In addition, a mass liquid yield of 100% is achieved.

Further examples of the performance of catalyst structures for upgrading hydrocarbons in a reaction System as depicted in FIG. 1 are depicted in Table 4. The catalysts used for each process described in Table 4 are all lwt.%Ag-lwt.%Ga/HZSM-5(23:l) (formed utilizing a process as described in Example 1). All catalysts were in the pellet form and ail reactions were performed in a continuous fixed bed reactor (similar to the test performed in Example 1). The catalyst used in the entry 14 was a regenerated one with the following régénération process: rinsing the catalyst structure with toluene;drying the rinsed catalyst structure in air to remove toluene from the catalyst structure; and heating the dried catalyst structure in air at a température of at least about 500 °C for a time period of at least about 3 hours.The upgrading processes were performed in the presence of methane, nitrogen or hydrogen, where the operating conditions in the reactor are further described for each example, as well as the initial and final viscosities of the oil that is upgraded and the liquid yield. As can be seen in the data provided in Table 4, the upgraded oil product in each example has 25 a reduced or lower viscosity in relation to the starting or raw oil for each process performed in methane, nitrogen or hydrogen, and the liquid yield is also very high for each ex amp le.

Table 4 - Further cxamples ofheavy oil upgrading process

Entry	T emperature /°C	Pressure /MPa	Gas	Viscosity of Raw Oil /mPa-s	Viscosity of Product oil / mPas	Liquid yield/%
l	410	10	ch4	1,911	179	103
2	420	5	ch4	345	46	101
3	400	3	ch4	111,917	370	99
4	400	5	ch4	111,917	349	98
5	400	8	ch4	111,917	247	97
6	400	10	ch4	111,917	245	101
7	410	10	ch4	111,917	225	106
8	420	5	ch4	111,917	205	109
9	420	10	ch4	111,917	151	97
10	380	5	ch4	111,917	589	102
11	400	5	n2	111,917	1,009	104
12	420	5	n2	111,917	S87	98
13	400	5	h2	111,917	223	99
14	400	3	ch4	111,917	530	98

The upgrading processes as described herein therefore facilitate the formation of a second (upgraded) hydrocarbon product from a first hydrocarbon product. Some non-limiting examples of types of upgraded hydrocarbon products that can be formed utilizing an upgrading process with a catalyst structure as described herein include:

— A method of upgrading a heavy oil that comprises receiving a feedstock of heavy oil in a reactor and reacting the heavy oil in the reactor in the présence of a gas and a catalyst structure as described herein to produce an oil product, where the gas comprises methane, hydrogen or nitrogen and one or more of the following change in properties between the heavy oil and the oî! product is achieved: a viscosity of the oil product is less than a viscosity of the heavy oil, a density of the product oil product is less than a density of the heavy oil, a sulfur content of the oil product is less than a sulfur content of the heavy oil, a TAN of the oil product is less than a TAN of the heavy oil, an aromatic content of the oil product is greater than an aromatic content of the heavy oil, an asphaltene content of the oil product is less than an asphaltene content of the heavy oil, a H/C ratio of the oil product is greater than a H/C ratio of the heavy oit, and/or a nitrogen content of the oil product is less than a nitrogen content of the heavy oil.

— A method of upgrading a light oil that comprises receiving a feedstock of light oil in a reactor and reacting the light oil in the reactor in the presence of a gas and a catalyst structure as described herein to produce an oil product, where the gas comprises methane, hydrogen or nitrogen and one or more of the following change in properties between the light oil and the oil product is achieved: a sulfur content of the oil product is less than a sulfur content of the light oil, a nitrogen content of the oil product is less than a nitrogen content of the light oil, an aromatic content of the oil product is greater than an aromatic content of the light oil, and/or a pour point of the oil product is less than a pore point of the light oil (which facilitâtes pipelining of light oils that are solid at room température).

— A method of upgrading a resid that comprises receiving a feedstock of resid in a reactor and reacting the resid in the reactor in the presence of a gas and a catalyst structure as described herein to produce a resid product, where the gas comprises methane, hydrogen or nitrogen and one or more of the following change in properties between the resid and the resid product is achieved: an aromatics content of the résidé product is greater than an aromatics content of the resid, a viscosity of the résidé product is less than a viscosity of the resid, a density of the résidé product is less than a density of the resid, a TAN of the resid product is less than a TAN of the resid, a H/C ratio of the resid product is greater than a H/C ratio of the resid, and/or a nitrogen content of the resid product is less than a nitrogen content of the resid, — A method of upgrading a gasoline that comprises receiving a feedstock of gasoline in a reactor and reacting the gasoline in the reactor in the presence of a gas and a catalyst structure as described herein to produce a gasoline product, where the gas comprises methane, hydrogen or nitrogen and at least the following change in properties between the gasoline and the gasoline product is achieved: an aromatics content of the gasoline product is greater than an aromatics content of the gasoline, and/or an octane number of the gasoline product is greater than an octane number of the gasoline.

— A method of upgrading a diesel fuel that comprises receiving a feedstock of diesel fuel in a reactor and reacting the diesel fuel in the reactor in the presence of a gas and a catalyst structure as described herein to produce a diesel fuel product, where the gas comprises methane, hydrogen or nitrogen and one or more of the following change in properties between the diesel fuel and the diesel fuel product is achieved: a sulfur content of the diesel fuel product is less than a sulfur content of the diesel fuel, and/or a cetane number of the diesel fuel product is greater than a cetane number of the diesel fuel.

— A method of upgrading a jet fuel that comprises receiving a feedstock of jet fuel in a reactor and reacting the jet fuel in the reactor in the presence of a gas and a catalyst structure as described herein to produce a jet fuel product, where the gas comprises methane, hydrogen or nitrogen and one or more of the following change in properties between the jet fuel and the jet fuel product is achieved: an aromatics content of the jet fuel product is greater than an aromatics content of the jet fuel (this feature is typîcally désirable to ensure proper seals in jet engines), and/or a sulfur content of the jet fuel product is less than a sulfur content of the jet fuel.

— A method of upgrading a bunker fuel that comprises receiving a feedstock of bunker fuel in a reactor and reacting the bunker fuel in the reactor in the presence of a gas and a catalyst structure as described herein to produce a bunker fuel product, where the gas comprises methane, hydrogen or nitrogen and at least the following change in properties between the bunker fuel and the bunker fuel product is achieved: a sulfur content of the bunker fuel product is less than the sulfur content of the bunker fuel.

— A method of upgrading a bio oil that comprises receiving a feedstock of bio oil in a reactor and reacting the bio oil in the reactor in the presence of a gas and a catalyst structure as described herein to produce a bio oil product, where the gas comprises methane, hydrogen or nitrogen and at least the following change in properties between the bio oil and the bio oil product is achieved: an oxygen content of the bio oil product is less than an oxygen content of the bio oïl, and a H/C ratio of the bio oil product is greaterthan a H/C ratio of the bio oil.

— A method of upgrading an FT (Fischer-Tropsch) wax and oil that comprises receiving a feedstock of the FT wax and oîl in a reactor and reacting the FT wax and oil in the reactor in the presence of a gas and a catalyst structure as described herein to produce a FT wax and oil product, where the gas comprises methane, hydrogen or nitrogen and at least one of the following change in properties between the FT wax and oil and the FT wax and oîl product is achieved: a viscosity of the FT wax and oil product is less than a viscosity of the FT wax and oil, a sulfur content of the FT wax and oil product is less than the sulfur content of the FT wax and oil, an olefin content of the FT wax and oil product is less than an olefin content of the FT wax and oil, and/or a pour point of the FT wax and oil product is less than a pore point of the FT wax and oil.

- A method of upgrading a feedstock that comprises receiving a feedstock of oil in a reactor and reacting the oîl in the reactor in the presence of a gas and a catalyst structure as described herein to produce an oil product, where the gas comprises methane, hydrogen or nitrogen and one or more of the following change in properties between the oil and the oil product is achieved: a viscosity of the oil product is less than a viscosity of the heavy oil, a density of the product oil product is less than a density of the heavy oîl, a sulfur content of the oil product is less than a sulfur content of the heavy oil, a TAN of the oil product is less than a TAN of the heavy oil, an aromatic content of the oil product is greater than an aromatic content of the oil, with the purpose of producing an extender oil or softening oil , which is added to rubber compounds in the production process for tires and other rubber goods to achieve an acceptable process ability.

Whîle the invention has been described in detail and with reference to spécifie embodiments thereof, it will be apparent to one skilled in the art that various changes and modifications can be made therein without departing from the spirit and scope thereof.

Thus, it is intended that the présent invention covers the modifications and variations of this invention provided they corne within the scope of the appended ciaims and their équivalents.

Claims (22)

1. A catalyst structure comprising:

a porous support structure comprising an aluminosilicate material, and a plurality of metals loaded in the porous support structure, the plurality of mêlais including at least three metals selected from the group consîsting of:

Ga, Ag, Zn, Co and Ce, or

Ga, Ag, Mo, Zn and Co;

wherein each métal loaded in the porous support structure is présent in an amount from about 0.1 wt% to about 20 wt%.

2. The catalyst structure of claim 1, wherein the porous support structure comprises an aluminosilicate material with a ratio of Silicon oxide to ahiminum oxide from 1:1 to 280:1.

3. The catalyst structure of claim 1, wherein the metals loaded within the porous support structure include Ga, Ag, Mo, Co and Ce.

4. The catalyst structure of claim 1, wherein the porous support structure comprises an aluminosilicate material having the following metals loaded in the porous support structure at the foliowîng weight percentages:

Ag: 1 wt%;

Ga: 1 wt%;

Co: 2 wt%;

Mo: 6 wt%; and

Ce: 10 wt%.

5. The catalyst structure of claim 1, wherein the porous support structure comprises an aluminosilicate material having the following metals loaded in the porous support structure at the following weight percentages:

Ag: 1 wt%;

Ga: 1 wt%;

Mo: 5 wt%; and

Ce: 10 wt%.

6. A method of forming the catalyst structure of claim 1, the method comprising:

dissol ving three or more métal salts in water to form a métal precursor solution, the two or more métal salts including the three or more metals;

loading the métal precursor solution into the porous support structure;

drying the support structure loaded with métal precursor for a period of at least 2 hours at a température from about 80 °C to about 120 °C; and calcining the dried support structure loaded with métal precursor at a température ranging from about 300 °C to about 700 °C and at a heating rate that increases in an amount ranging from about 5 “C/min to about 20 °C/min.

7. The method of claim 6, further comprising regenerating the catalyst structure by performing the following steps:

rinsing the catalyst structure with toluene;

drying the rinsed catalyst structure in air to remove toluene from the catalyst structure; and heating the dried catalyst structure in air at a température of at least about 500 ^ÛC for a time period of at least about 3 hours.

8. The method of claim 7, further comprising repeating the regenerating ofthe catalyst structure a pîurality of times.

9. The method of claim 8, wherein the porous support structure comprises a pîurality of granules such that the catalyst structure is formed as a powder.

10. The method of claim 9, further comprising, after calcination, forming a pellet from the catalyst structure by:

combining the catalyst structure in powder form with a binder material in an acidic solution to form a mixture;

extruding the mixture through a forming die to form an extruded element; and drying and caldning the extruded element to form thepellet,

11. The method of claim 10. wherein the binder material comprises colloïdal silica and methyl cellulose, the acidic solution comprises acetic acid or citric acid.

12. The method of claim 1 1, wherein the combining further comprises:

combining the catalyst structure in powder form with methyl cellulose and the acid solution to form a first mixture; and combining colloïdal silica with the first mixture to form a second mixture to be extruded through the forming die.

13. The method of claim 11, wherein the mixture comprises the following:

a weight ratio of catalyst powder to colloïdal silica that ranges from 1:0.5 to 1:2;

a weight ratio of catalyst powder to methyl cellulose that ranges from 1:0.05 to 1:0.2; and a weight ratio of catalyst powder to acid solution that ranges from 1:0.1 to 1:0.5.

14. A method of upgrading a first hydrocarbon product to form a second hydrocarbon product, the method comprising:

receiving a feedstock of the first hydrocarbon product in a reactor; and reacting the first hydrocarbon product in the reactor in the presence of a gas and the catalyst structure of claim 1 to produce the second hydrocarbon product, wherein the gas comprises methane, hydrogen or nitrogen, and one or more properties of the second hydrocarbon product is changed in relation to the first hydrocarbon product.

15. The method of claim 14, wherein the reactor comprises one or a combination of the following: a batch reactor System, a continuons tubular reactor (CTR), a continuons stirred-tank reactor (CSTR), a semi batch reactor, and a non-thermal plasma reactor.

16. The method of claim 15, wherein the catalyst structure is provided within the reactor in the form of a fïxed bed, a trickle-bed, a moving bed, a rotatîng bed, a fluidized bed, or as a slurry.

17. The method of claim 14, wherein a reaction température within the reactor is within a range of about 300 °C to about 500 °C.

18. The method of claim 17, wherein a pressure within the reactor is between about 1 atm and about 200 atm.

19. The method of claim 14, wherein the reactor comprises a batch reactor, and a mass ratio of heavy oil feedstock to catalyst structure is from about 200:1 to about 1:10.

20. The method of claim 14, wherein the reactor comprises a continuons flow reactor, and a liquid hourly space velocîty (LHSV) of the heavy oil feedstock is in a range from about 0.1 h'¹ to about L00 h'¹.

21. The method of claim 14, wherein the one or more properties of the second hydrocarbon product that is changed in relation to the first hydrocarbon product is selected from the group consisting of viscosity, density, suifur content, amount of olefins, amount of one or more aromatic hydrocarbons, amount of one or more paraffins, total acid number (TAN), hydrogen to carbon ratio, and cetane number.

22. The method of claim 14, further comprising, after the reacting of the first hydrocarbon product in the reactor in the presence of the gas and the catalyst structure to produce the second hydrocarbon product, regenerating the catalyst structure by perfonning the following steps:

rinsing the catalyst structure with toluene;

drying the rinsed catalyst structure in air to remove toluene from the catalyst structure; and heatîng the dried catalyst structure in air at a température of at least about 500 °C for a time period of at least about 3 hours.