Patent Application
20240391855
The present invention belongs to the field of petrochemical industry, and specifically relates to a method for producing benzene, toluene and p-xylene by coupling conversion of naphtha and CO2, in particular to a method for producing benzene, toluene and p-xylene by coupling conversion of naphtha and CO2 under catalysis of a modified zeolite molecular sieve catalyst.
With the development of industry, the amount of carbon dioxide (CO2) in atmosphere is constantly increasing, leading to a more and more serious greenhouse effect. In response to the international concept of “carbon neutrality”, recycling of CO2 has become the research focus of scientific research personnel.
In addition, benzene, toluene and xylene (hereinafter referred to as BTPX) are basic chemicals, which have large market consumption and need to be imported in large quantities in China. At present, a technical route of producing BTPX mainly involves catalytic reforming of naphtha. However, the technical route still cannot meet demands in China.
Although researchers have found that hydrogenation of carbon dioxide under the action of hydrogen can be used for producing BTPX, this route is used for producing liquid hydrocarbons or BTPX by hydrogenation of carbon dioxide, technical indicators are difficult to achieve, and sources of hydrogen have become a key problem limiting industrial application.
In order to solve the above technical problems, the inventor of the present application has creatively found that coupling of naphtha as a raw material and CO2 as a raw material to produce benzene, toluene and p-xylene is a new technical route of producing aromatic benzene, toluene and p-xylene by means of CO2, which provides a new way for production of benzene, toluene and p-xylene and large-scale utilization of CO2.
On the one hand, the present application provides a method for preparing a modified molecular sieve catalyst used for catalyzing coupling conversion of naphtha and CO2 to produce benzene, toluene and p-xylene, where the method includes subjecting a molecular sieve to metal modification by using a high temperature hydrothermal method, including the following steps:
Optionally, the solid-liquid ratio of the zeolite molecular sieve to be metal-modified to the soluble metal salt aqueous solution is 1/10 to 1/1, and the mass concentration of a metal salt in the soluble metal salt aqueous solution is in a range from 10% to 30%; the impregnating time is in a range from 2 hours to 10 hours; the step of drying is carried out in an air atmosphere at temperature in a range from 100° C. to 150° C.; and the step of calcination is carried out in an air atmosphere at temperature in a range from 500° C. to 700° C.
Optionally, in step (1), the soluble metal salt aqueous solution is heated to any value or a range value determined by any two values of the following temperatures: 60° C., 70° C., 80° C., 90° C. and 100° C.
Optionally, in step (2), the impregnating time is any value or a range value determined by any two values of the following times: 2 hours, 4 hours, 6 hours, 8 hours and 10 hours.
Optionally, a metal used for the metal modification is at least one selected from a group of La, Zn, Ga, Fe, Mo and Cr metals.
Optionally, the metal modification includes modification with a duplex metal of Zn and Ga.
Optionally, the modified zeolite molecular sieve catalyst consists of a modified HZSM-5 zeolite molecular sieve.
Optionally, the modified zeolite molecular sieve catalyst includes a modified HZSM-5 zeolite molecular sieve and a binder.
Optionally, the method further includes subjecting the molecular sieve to silanization modification after the metal modification.
Optionally, the silanization modification is carried out by using an in situ chemical vapor deposition method, which includes the following steps:
Optionally, in step (6), the temperature of the reactor is raised to a range from 400° C. to 550° C., and the air is introduced for calcination.
Specifically, the silanization modification is carried out by using an in situ chemical vapor deposition method, which includes the following steps:
Optionally, the silanization modification is carried out by using an in situ vapor atomic layer deposition method, which includes the following steps:
Specifically, the silanization modification is carried out by using an in situ vapor atomic layer deposition method, which includes the following steps:
Optionally, “in situ” in the “in situ chemical vapor deposition method” and the “in situ vapor atomic layer deposition method” refers to catalysis of a coupling conversion reaction of naphtha and CO2 in the same reactor without the step of removing the modified molecular sieve after the silanization modification of the molecular sieve in the reactor. The in situ vapor silanization method reduces the steps of transportation, loading and washing of a catalyst, and greatly reduces the cost.
Optionally, the silanization reagent used for the silanization modification is selected from at least one of compounds with the following chemical formula:
where R1, R2, R3 and R4 are independently selected from C1-10 alkyl and C1-10 alkoxyl.
Optionally, according to the silanization reagent used for the silanization modification, at least one of the R1, the R2, the R3 and the R4 is selected from C1-10 alkoxyl.
Optionally, the silanization reagent is selected from at least one of tetraethyl silicate and tetramethyl silicate.
On the other hand, the present application provides a method for producing benzene, toluene and p-xylene by coupling conversion of naphtha and CO2, where the method includes: (a) preparing a modified molecular sieve catalyst by the above method; and (b) enabling a raw material containing naphtha and CO2 to contact with the modified molecular sieve catalyst in a reactor for a reaction to produce benzene, toluene and p-xylene.
Optionally, the modified zeolite molecular sieve is a zeolite molecular sieve obtained by metal modification and silanization modification.
Optionally, the modified zeolite molecular sieve is a zeolite molecular sieve obtained by carrying out metal modification first and then carrying out silanization modification.
Optionally, the modified zeolite molecular sieve is a zeolite molecular sieve obtained only by silanization modification.
Optionally, the zeolite molecular sieve catalyst consists of a modified zeolite molecular sieve.
Optionally, the modified zeolite molecular sieve is a zeolite molecular sieve obtained by sequentially carrying out metal modification, silanization modification and in situ water vapor modification.
Specifically, the water vapor modification is carried out in the following steps: introducing water vapor into a reactor where a molecular sieve obtained by in situ silanization modification is placed, and raising the temperature to a range from 700° C. to 900° C. in a nitrogen atmosphere for treatment for predetermined time.
Optionally, the raw material consists of naphtha and CO2.
Optionally, the naphtha is at least one selected from a group of hydrocracked naphtha, catalytic cracked naphtha, raffinate oil, topped oil and direct coal liquefied naphtha.
Optionally, the carbon number distribution of hydrocarbons in the naphtha is in a range of C4-C12.
Optionally, the reactor is one of a fixed bed reactor, a fluidized bed reactor or a moving bed reactor.
Optionally, conditions for the reaction of the naphtha and the CO2 are as follows: the reaction temperature is in a range from 450° C. to 650° C., the reaction pressure is in a range from 0.1 MPa to 3 MPa, the weight hourly space velocity of the naphtha is in a range from 0.1 h−1 to 5 h−1, and the weight hourly space velocity of the CO2 is in a range from 0.1 h−1 to 5 h−1.
Optionally, the reaction temperature is selected from any value of 450° C., 500° C., 550° C. and 650° C., or a range value determined by any two of the values.
Optionally, the reaction pressure is selected from any value of 0.1 MPa, 1 MPa and 3 MPa, or a range value determined by two of the values.
Optionally, the weight hourly space velocity of the naphtha is selected from any value of 0.1 h−1, 1 h−1 and 5 h−1, or a range value determined by any two of the values.
Optionally, the weight hourly space velocity of the CO2 is selected from any value of 0.1 h−1, 0.3 h−1 and 5 h−1, or a range value determined by any two of the values.
Optionally, the reaction time is in a range from 30 minutes to 120 minutes.
Optionally, the mass ratio of the CO2 to the naphtha is 0.8:0.27 to 0.8:1;
Optionally, the zeolite molecular sieve catalyst further includes a binder.
In the present application, a method for preparing a zeolite molecular sieve catalyst used in a fluidized bed includes: uniformly mixing a metal-modified zeolite molecular sieve with a binder in water, carrying out beating, milling and defoaming to obtain slurry, and subjecting the obtained slurry to conventional spray drying, molding and calcination to obtain the zeolite molecular sieve used in the fluidized bed; where the binder includes an amorphous binder containing aluminum or silicon, preferably pseudo-boehmite or silica sol.
Specifically, the method for producing BTPX by coupling conversion of naphtha and CO2 includes:
The “hydrocracked naphtha” of the present application refers to heavy naphtha produced by a hydrocracking reaction of heavy oil.
The “catalytic cracked naphtha” of the present application refers to naphtha produced by catalytic cracking of vacuum gas oil and atmospheric residue.
The “raffinate oil” of the present application refers to distillate remaining after aromatic hydrocarbon extraction of a catalytic reforming product rich in aromatic hydrocarbons.
The “topped oil” of the present application refers to a light fraction with a boiling point of lower than 60° C. obtained by distillation of straight-run gasoline.
The “direct coal liquefied naphtha” of the present application refers to naphtha produced by a direct coal liquefaction device.
In the present application, the coupling conversion of naphtha and CO2 to produce aromatic hydrocarbons refers to a reaction of the CO2 as a raw material and the naphtha to produce aromatic hydrocarbons.
On another hand, the present application provides a method for silanization modification of a molecular sieve catalyst, where the method includes the following steps:
Specifically, the silanization modification is carried out by using an in situ vapor atomic layer deposition method, which includes the following steps:
On another hand, the present application provides a method for modifying a molecular sieve catalyst, where the method includes the following steps:
Optionally, the solid-liquid ratio of the modified zeolite molecular sieve to the soluble metal salt aqueous solution is 1/10 to 1/1 (mass ratio), and the mass concentration of a metal salt in the soluble metal salt aqueous solution is in a range from 10% to 30%; the impregnating time is 2-10 hours; the step of drying is carried out in an air atmosphere at 100-150° C.; and the step of calcination is carried out in an air atmosphere at temperature in a range from 500° C. to 700° C.
Optionally, in step (1), the soluble metal salt aqueous solution is heated to any value or a range value determined by any two values of the following temperatures: 60° C., 70° C., 80° C., 90° C. and 100° C.
Optionally, in step (2), the impregnating time is any value or a range value determined by any two values of the following times: 2 hours, 4 hours, 6 hours, 8 hours and 10 hours.
Optionally, the zeolite molecular sieve is an HZSM-5 hydrogen type molecular sieve.
Optionally, a metal in the metal-modified zeolite molecular sieve is at least one selected from a group of La, Zn, Ga, Fe, Mo and Cr metals.
Optionally, the silanization reagent used for the silanization modification is selected from at least one of compounds with the following chemical formula:
where R1, R2, R3 and R4 are independently selected from C1-10 alkyl and C1-10 alkoxyl.
Optionally, at least one of the R1, the R2, the R3 and the R4 is selected from C1-10 alkoxyl.
Optionally, the silanization reagent is selected from at least one of tetraethyl silicate and tetramethyl silicate.
The present application has the following beneficial effects.
(1) The present application provides a new technical route for large-scale production of benzene, toluene and p-xylene (BTPX) by means of CO2, and the method overcomes the defects of limited hydrogen resources and high costs of existing technologies.
(2) In the present application, with a modified HZSM-5 molecular sieve as an active component of a catalyst, the selectivity of BTPX in hydrocarbon products is as high as 75.08%, and the selectivity of p-xylene in xylene is 92% or above.
(3) In the present application, compared with the use of an HZSM-5 molecular sieve obtained only by metal modification as an active component of a catalyst, the use of an HZSM-5 molecular sieve obtained by metal modification and silanization modification as an active component of a catalyst can achieve higher selectivity of BTPX and higher selectivity of p-xylene in xylene.
(4) In the present application, compared with the use of an in situ chemical vapor deposition method for silanization, the use of an in situ vapor atomic layer deposition method for silanization modification has the advantages that the modified HZSM-5 molecular sieve as an active component can achieve higher selectivity of BTPX and higher selectivity of p-xylene in xylene.
The present application is described in detail below in conjunction with examples, but the present application is not limited to the examples.
Endpoints and any values of ranges disclosed in the present application are not limited to the exact ranges or values, and these ranges or values should be understood as including approximate ranges or values. For numeric ranges, endpoint values and individual point values of each range may be combined with each other to obtain one or more new numeric ranges, and these numeric ranges should be considered to be specifically disclosed herein.
The present application is described in detail below in conjunction with examples, but the present application is not limited to the examples.
Unless otherwise specified, raw materials used in the examples of the present application are purchased by commercial ways or prepared by known methods. An HZSM-5 zeolite molecular sieve used in the examples was purchased from Nankai Catalyst Factory.
Unless otherwise specified, analytical methods used in the examples are implemented with conventional setup of instruments or equipment and are conventional analytical methods.
In the examples of the present application, the type of naphtha is direct coal liquefied naphtha, which includes specific components as shown in the following table.
In the examples of the present application, the inner diameter of a fixed bed reactor is 1.5 cm; and the inner diameter of a fixed fluidized bed reactor is 3 cm.
In the examples of the present application, only hydrocarbon products are listed, and other products obtained by a reaction of naphtha and CO2 are not listed.
100 g of an HZSM-5 zeolite molecular sieve (Nankai Catalyst Factory, Si/Al=15) was placed in a 10 wt % zinc nitrate aqueous solution, where the mass ratio (namely solid-liquid ratio) of the HZSM-5 zeolite molecular sieve to the zinc nitrate aqueous solution was 1/10. The molecular sieve was impregnated at 80° C. for 6 hours, drained, dried in an air atmosphere at 120° C. for 4 hours, and then calcined in an air atmosphere at 550° C. for 4 hours to obtain a [Zn]HZSM-5 molecular sieve sample. Then, the sample was subjected to pressing molding, crushed and sieved to obtain molded molecular sieve particles with a particle size of 40-60 mesh, recorded as FX-[Zn]HZSM-5.
100 g of an HZSM-5 zeolite molecular sieve (Nankai Catalyst Factory, Si/Al=15) was placed in a 10 wt % gallium nitrate aqueous solution, where the mass ratio (namely solid-liquid ratio) of the HZSM-5 zeolite molecular sieve to the gallium nitrate aqueous solution was 1/10. The molecular sieve was impregnated at 80° C. for 6 hours, drained, dried in an air atmosphere at 120° C. for 4 hours, and then calcined in an air atmosphere at 550° C. for 4 hours to obtain a [Ga]HZSM-5 molecular sieve sample. Then, the sample was subjected to pressing molding, crushed and sieved to obtain molded molecular sieve particles with a particle size of 40-60 mesh, recorded as FX-[Ga]HZSM-5.
100 g of an HZSM-5 zeolite molecular sieve (Nankai Catalyst Factory, Si/Al=15) was placed in a 10 wt % lanthanum nitrate aqueous solution, where the mass ratio (namely solid-liquid ratio) of the HZSM-5 zeolite molecular sieve to the lanthanum nitrate aqueous solution was 1/10. The molecular sieve was impregnated at 90° C. for 4 hours, drained, dried in an air atmosphere at 120° C. for 4 hours, and then calcined in an air atmosphere at 550° C. for 4 hours to obtain a [La]HZSM-5 molecular sieve sample. Then, the sample was subjected to pressing molding, crushed and sieved to obtain molded molecular sieve particles with a particle size of 40-60 mesh, recorded as FX-[La]HZSM-5.
100 g of an HZSM-5 zeolite molecular sieve (Nankai Catalyst Factory, Si/Al=15) was placed in a 10 wt % ferric nitrate aqueous solution, where the mass ratio (namely solid-liquid ratio) of the HZSM-5 zeolite molecular sieve to the ferric nitrate aqueous solution was 1/10. The molecular sieve was impregnated at 70° C. for 8 hours, drained, dried in an air atmosphere at 120° C. for 4 hours, and then calcined in an air atmosphere at 550° C. for 4 hours to obtain a [Fe]HZSM-5 molecular sieve sample. Then, the sample was subjected to pressing molding, crushed and sieved to obtain molded molecular sieve particles with a particle size of 40-60 mesh, recorded as FX-[Fe]HZSM-5.
100 g of an HZSM-5 zeolite molecular sieve (Nankai Catalyst Factory, Si/Al=15) was placed in a 10 wt % chromium nitrate aqueous solution, where the mass ratio (namely solid-liquid ratio) of the HZSM-5 zeolite molecular sieve to the chromium nitrate aqueous solution was 1/10. The molecular sieve was impregnated at 70° C. for 8 hours, drained, dried in an air atmosphere at 120° C. for 4 hours, and then calcined in an air atmosphere at 550° C. for 4 hours to obtain a [Cr]HZSM-5 molecular sieve sample. Then, the sample was subjected to pressing molding, crushed and sieved to obtain molded molecular sieve particles with a particle size of 40-60 mesh, recorded as FX-[Cr]HZSM-5.
100 g of the [Zn]HZSM-5 molecular sieve sample prepared in Example 1 was mixed with an amorphous binder containing aluminum or silicon for spray drying and molding. Specific steps are as follows.
The [Zn]HZSM-5 molecular sieve sample, pseudo-boehmite, silica sol, xanthan gum (biological gum) and water were uniformly mixed, followed by beating, milling and defoaming to obtain slurry. The slurry includes the following parts by weight of components:
The obtained slurry was subjected to spray drying and molding to obtain a microsphere particle sample with the particle size distribution of 20-100 m. Then, the microsphere particle sample was calcined in a Muffle furnace at 550° C. for 3 hours to obtain a [Zn]HZSM-5 molded molecular sieve with an abrasion index of 1.2, recorded as FL-[Zn]HZSM-5.
100 g of an HZSM-5 zeolite molecular sieve (Nankai Catalyst Factory, Si/Al=15) was placed in a 10 wt % mixed aqueous solution of zinc nitrate and gallium nitrate, where the mass ratio of the zinc nitrate to the gallium nitrate was 1/1, and the mass ratio (namely solid-liquid ratio) of the HZSM-5 zeolite molecular sieve to the mixed aqueous solution of the zinc nitrate and the gallium nitrate was 1/10. The molecular sieve was impregnated at 80° C. for 6 hours, drained, dried in an air atmosphere at 120° C. for 4 hours, and then calcined in an air atmosphere at 550° C. for 4 hours to obtain a [Zn,Ga]HZSM-5 molecular sieve sample. Then, the sample was subjected to pressing molding, crushed and sieved to obtain molded molecular sieve particles with a particle size of 40-60 mesh, recorded as FX-[Zn,Ga]HZSM-5.
100 g of an HZSM-5 zeolite molecular sieve (Nankai Catalyst Factory, Si/Al=15) was placed in a 10 wt % zinc nitrate aqueous solution, where the mass ratio (namely solid-liquid ratio) of the HZSM-5 zeolite molecular sieve to the zinc nitrate aqueous solution was the same as that in Example 1. The molecular sieve was impregnated at room temperature (20° C.) for 6 hours, drained, dried in an air atmosphere at 120° C. for 4 hours, and then calcined in an air atmosphere at 550° C. for 4 hours to obtain a [Zn]HZSM-5 molecular sieve sample. Then, the sample was subjected to pressing molding, crushed and sieved to obtain molded molecular sieve particles with a particle size of 40-60 mesh, recorded as FX-[Zn]HZSM-5-R.
100 g of an HZSM-5 zeolite molecular sieve (Nankai Catalyst Factory, Si/Al=15) was placed in a 10 wt % zinc nitrate aqueous solution, where the mass ratio (namely solid-liquid ratio) of the HZSM-5 zeolite molecular sieve to the zinc nitrate aqueous solution was 1/1. The molecular sieve was impregnated at 80° C. for 6 hours, drained, dried in an air atmosphere at 120° C. for 4 hours, and then calcined in an air atmosphere at 550° C. for 4 hours to obtain a [Zn]HZSM-5 molecular sieve sample. Then, the sample was subjected to pressing molding, crushed and sieved to obtain molded molecular sieve particles with a particle size of 40-60 mesh, recorded as FX-[Zn]HZSM-5-A.
A catalyst used for coupling conversion of naphtha and CO2 to produce benzene, toluene and p-xylene was prepared on-line in a micro-fixed bed reactor. Conditions for on-line preparation of the catalyst are as follows. 5 g of the FX-[Zn]HZSM-5 catalyst prepared in Example 1 was loaded into a fixed bed reactor, treated with nitrogen at 50 ml/min at 550° C. for 1 hour, and then cooled to 300° C. in a nitrogen atmosphere. In the nitrogen atmosphere (controlled by a mass flow meter, 100 mL/min), tetraethyl silicate was pumped into the reactor at a weight hourly space velocity of 0.2 h−1 at normal pressure. After feeding for 60 minutes, the feeding was stopped, where the introduced amount of the tetraethyl silicate was 0.2 g/g the catalyst. A resulting mixture was purged with nitrogen, heated to 550° C., and then calcined in an air atmosphere for 4 hours to obtain a fixed bed catalyst used for coupling conversion of naphtha and CO2 to produce benzene, toluene and p-xylene, named as FXNCC-1.
Then, the temperature was adjusted to a reaction temperature of 550° C. in a nitrogen atmosphere. A raw material naphtha was fed by a micro-feed pump, and the flow of CO2 was controlled by a mass flow meter. The mass ratio of the raw material CO2 to the naphtha was 0.8:1, the weight hourly space velocity of the CO2 was 0.8 h−1, the weight hourly space velocity of the naphtha was 1.0 h−1, and the reaction pressure was 0.1 MPa. Reaction products were analyzed by on-line Agilent7890 gas chromatography, and sampling was carried out for analysis when a reaction was carried out for 30 minutes. Reaction results are shown in Table 1.
The reaction performance of a catalyst used for coupling conversion of naphtha and CO2 was evaluated in a micro-fixed bed reactor. Evaluation conditions are as follows. 5 g of the FX-[Zn]HZSM-5 prepared in Example 1 was loaded into a fixed bed reactor, and treated with nitrogen at 50 ml/min at 550° C. for 1 hour.
Then, the temperature was adjusted to a reaction temperature of 550° C. in a nitrogen atmosphere. A raw material naphtha was fed by a micro-feed pump, and the flow of CO2 was controlled by a mass flow meter. The mass ratio of the raw material CO2 to the naphtha was 0.8:1, the weight hourly space velocity of the CO2 was 0.8 h−1, the weight hourly space velocity of the naphtha was 1.0 h−1, and the reaction pressure was 0.1 MPa. Reaction products were analyzed by on-line Agilent7890 gas chromatography, and sampling was carried out for analysis when a reaction was carried out for 30 minutes. Reaction results are shown in Table 1-1.
As can be seen by comparing Example 10 and Example 10-1, compared with the use of the HZSM-5 molecular sieve obtained only by metal modification as an active component of the catalyst, the use of the HZSM-5 molecular sieve obtained by metal modification and silanization modification as an active component of the catalyst can achieve higher selectivity of BTPX and higher selectivity of p-xylene in xylene.
A catalyst used for coupling conversion of naphtha and CO2 to produce benzene, toluene and p-xylene was prepared on-line in a micro-fixed bed reactor. Conditions for on-line preparation of the catalyst are as follows. 5 g of the FX-[Ga]HZSM-5 catalyst prepared in Example 2 was loaded into a fixed bed reactor, treated with nitrogen at 50 ml/min at 550° C. for 1 hour, and then cooled to 300° C. in a nitrogen atmosphere. In the nitrogen atmosphere (controlled by a mass flow meter, 100 mL/min), tetraethyl silicate was pumped into the reactor at a weight hourly space velocity of 0.2 h−1 at normal pressure. After feeding for 60 minutes, the feeding was stopped, where the introduced amount of the tetraethyl silicate was the same as that in Example 10. A resulting mixture was purged with nitrogen, heated to 550° C., and then calcined in an air atmosphere for 4 hours to obtain a fixed bed catalyst used for coupling conversion of naphtha and CO2 to produce benzene, toluene and p-xylene, named as FXNCC-2.
Then, the temperature was adjusted to a reaction temperature of 550° C. in a nitrogen atmosphere. A raw material naphtha was fed by a micro-feed pump, and the flow of CO2 was controlled by a mass flow meter. The mass ratio of the raw material CO2 to the naphtha was 0.8:1, the weight hourly space velocity of the CO2 was 0.8 h−1, the weight hourly space velocity of the naphtha was 1.0 h−1, and the reaction pressure was 0.1 MPa. Reaction products were analyzed by on-line Agilent7890 gas chromatography, and sampling was carried out for analysis when a reaction was carried out for 30 minutes. Reaction results are shown in Table 2.
A catalyst used for coupling conversion of naphtha and CO2 to produce benzene, toluene and p-xylene was prepared on-line in a micro-fixed bed reactor. Conditions for on-line preparation of the catalyst are as follows. 5 g of the FX-[La]HZSM-5 catalyst prepared in Example 3 was loaded into a fixed bed reactor, treated with nitrogen at 50 ml/min at 550° C. for 1 hour, and then cooled to 300° C. in a nitrogen atmosphere. In the nitrogen atmosphere (controlled by a mass flow meter, 100 mL/min), tetraethyl silicate was pumped into the reactor at a weight hourly space velocity of 0.2 h−1 at normal pressure. After feeding for 60 minutes, the feeding was stopped, where the introduced amount of the tetraethyl silicate was the same as that in Example 10. A resulting mixture was purged with nitrogen, heated to 550° C., and then calcined in an air atmosphere for 4 hours to obtain a fixed bed catalyst used for coupling conversion of naphtha and CO2 to produce benzene, toluene and p-xylene, named as FXNCC-3.
Then, the temperature was adjusted to a reaction temperature of 550° C. in a nitrogen atmosphere. A raw material naphtha was fed by a micro-feed pump, and the flow of CO2 was controlled by a mass flow meter. The mass ratio of the raw material CO2 to the naphtha was 0.8:1, the weight hourly space velocity of the CO2 was 0.8 h−1, the weight hourly space velocity of the naphtha was 1.0 h−1, and the reaction pressure was 0.1 MPa. Reaction products were analyzed by on-line Agilent7890 gas chromatography, and sampling was carried out for analysis when a reaction was carried out for 30 minutes. Reaction results are shown in Table 3.
A catalyst used for coupling conversion of naphtha and CO2 to produce benzene, toluene and p-xylene was prepared on-line in a micro-fixed bed reactor. Conditions for on-line preparation of the catalyst are as follows. 5 g of the FX-[Fe]HZSM-5 catalyst prepared in Example 4 was loaded into a fixed bed reactor, treated with nitrogen at 50 ml/min at 550° C. for 1 hour, and then cooled to 300° C. in a nitrogen atmosphere. In the nitrogen atmosphere (controlled by a mass flow meter, 100 mL/min), tetraethyl silicate was pumped into the reactor at a weight hourly space velocity of 0.2 h−1 at normal pressure. After feeding for 60 minutes, the feeding was stopped, where the introduced amount of the tetraethyl silicate was the same as that in Example 10. A resulting mixture was purged with nitrogen, heated to 550° C., and then calcined in an air atmosphere for 4 hours to obtain a fixed bed catalyst used for coupling conversion of naphtha and CO2 to produce benzene, toluene and p-xylene, named as FXNCC-4.
Then, the temperature was adjusted to a reaction temperature of 550° C. in a nitrogen atmosphere. A raw material naphtha was fed by a micro-feed pump, and the flow of CO2 was controlled by a mass flow meter. The mass ratio of the raw material CO2 to the naphtha was 0.8:1, the weight hourly space velocity of the CO2 was 0.8 h−1, the weight hourly space velocity of the naphtha was 1.0 h−1, and the reaction pressure was 0.1 MPa. Reaction products were analyzed by on-line Agilent7890 gas chromatography, and sampling was carried out for analysis when a reaction was carried out for 30 minutes. Reaction results are shown in Table 4.
A catalyst used for coupling conversion of naphtha and CO2 to produce benzene, toluene and p-xylene was prepared on-line in a micro-fixed bed reactor. Conditions for on-line preparation of the catalyst are as follows. 5 g of the FX-[Cr]HZSM-5 catalyst prepared in Example 5 was loaded into a fixed bed reactor, treated with nitrogen at 50 ml/min at 550° C. for 1 hour, and then cooled to 300° C. in a nitrogen atmosphere. In the nitrogen atmosphere (controlled by a mass flow meter, 100 mL/min), tetraethyl silicate was pumped into the reactor at a weight hourly space velocity of 0.2 h−1 at normal pressure. After feeding for 60 minutes, the feeding was stopped, where the introduced amount of the tetraethyl silicate was the same as that in Example 10. A resulting mixture was purged with nitrogen, heated to 550° C., and then calcined in an air atmosphere for 4 hours to obtain a fixed bed catalyst used for coupling conversion of naphtha and CO2 to produce benzene, toluene and p-xylene, named as FXNCC-5.
Then, the temperature was adjusted to a reaction temperature of 550° C. in a nitrogen atmosphere. A raw material naphtha was fed by a micro-feed pump, and the flow of CO2 was controlled by a mass flow meter. The mass ratio of the raw material CO2 to the naphtha was 0.8:1, the weight hourly space velocity of the CO2 was 0.8 h−1, the weight hourly space velocity of the naphtha was 1.0 h−1, and the reaction pressure was 0.1 MPa. Reaction products were analyzed by on-line Agilent7890 gas chromatography, and sampling was carried out for analysis when a reaction was carried out for 30 minutes. Reaction results are shown in Table 5.
A catalyst used for coupling conversion of naphtha and CO2 to produce benzene, toluene and p-xylene was prepared on-line in a micro-fixed fluidized bed reactor. Conditions for on-line preparation of the catalyst are as follows. 10 g of the FX-[Zn]HZSM-5 catalyst prepared in Example 6 was loaded into a fixed fluidized bed reactor, treated with nitrogen at 50 ml/min at 550° C. for 1 hour, and then cooled to 300° C. in a nitrogen atmosphere. In the nitrogen atmosphere (controlled by a mass flow meter, 200 mL/min), tetraethyl silicate was pumped into the reactor at a weight hourly space velocity of 0.2 h−1 at normal pressure. After feeding for 75 minutes, the feeding was stopped, where the introduced amount of the tetraethyl silicate was 1.25 times of that in Example 9. A resulting mixture was purged with nitrogen, heated to 550° C., and then calcined in an air atmosphere for 4 hours to obtain a fixed bed catalyst used for coupling conversion of naphtha and CO2 to produce benzene, toluene and p-xylene, named as FLNCC-1. The purpose of using 10 g of the FL-[Zn]HZSM-5 molecular sieve molded sample in this example was only to meet requirements of the micro-fixed fluidized bed reactor, the amount (10 g) enables the catalyst to stay in a fluidized state, and the amount of 5 g cannot enable the catalyst to stay in a fluidized state. In a case of using the micro-fixed fluidized bed reactor, the feeding time was 75 min for silanization modification, which was only used to carry out silanization modification to the same degree as that in Example 9.
Then, the temperature was adjusted to a reaction temperature of 550° C. in a nitrogen atmosphere. A raw material naphtha was fed by a micro-feed pump, and the flow of CO2 was controlled by a mass flow meter. The mass ratio of the raw material CO2 to the naphtha was 0.8:1, the weight hourly space velocity of the CO2 was 0.8 h−1, the weight hourly space velocity of the naphtha was 1.0 h−1, and the reaction pressure was 0.1 MPa. Reaction products were analyzed by on-line Agilent7890 gas chromatography, and sampling was carried out for analysis when a reaction was carried out for 30 minutes. Reaction results are shown in Table 6.
A catalyst used for coupling conversion of naphtha and CO2 to produce benzene, toluene and p-xylene was prepared on-line in a micro-fixed bed reactor. Conditions for on-line preparation of the catalyst are as follows. 5 g of the FX-[Zn]HZSM-5 catalyst prepared in Example 1 was loaded into a fixed bed reactor, treated with nitrogen at 50 ml/min at 550° C. for 1 hour, and then cooled to 300° C. in a nitrogen atmosphere. Then, a vapor atomic layer deposition method was used to carry out modification with a silanization reagent, specifically including the following steps: (1) introducing nitrogen (controlled by a mass flow meter, 200 mL/min) into a saturated flask filled with tetraethyl silicate (temperature 15° C.), then introducing the same into a reactor, namely introducing the nitrogen carrying the tetraethyl silicate into the reactor, and after feeding for 5 minutes, stopping the feeding; (2) carrying out purging with nitrogen, and raising the temperature to 550° C., followed by calcination in an air atmosphere for 1 hour; and (3) repeating steps (1) and (2) for 3 times to obtain a fixed bed catalyst used for coupling conversion of naphtha and CO2 to produce benzene, toluene and p-xylene, named as FXNCC-6, where the amount of the tetraethyl silicate introduced for 4 times was equivalent to the amount introduced for one time in Example 10.
Then, the temperature was adjusted to a reaction temperature of 550° C. in a nitrogen atmosphere. A raw material naphtha was fed by a micro-feed pump, and the flow of CO2 was controlled by a mass flow meter. The mass ratio of the raw material CO2 to the naphtha was 0.8:1, the weight hourly space velocity of the naphtha was 1.0 h−1, and the reaction pressure was 0.1 MPa. Reaction products were analyzed by on-line Agilent7890 gas chromatography, and sampling was carried out for analysis when a reaction was carried out for 30 minutes. Reaction results are shown in Table 7.
A catalyst used for coupling conversion of naphtha and CO2 to produce benzene, toluene and p-xylene was prepared on-line in a micro-fixed bed reactor. Conditions for on-line preparation of the catalyst are as follows. 5 g of the FX-[Zn,Ga]HZSM-5 catalyst prepared in Example 7 was loaded into a fixed bed reactor, treated with nitrogen at 50 ml/min at 550° C. for 1 hour, and then cooled to 300° C. in a nitrogen atmosphere. In the nitrogen atmosphere (controlled by a mass flow meter, 100 mL/min), tetraethyl silicate was pumped into the reactor at a weight hourly space velocity of 0.2 h−1 at normal pressure. After feeding for 60 minutes, the feeding was stopped, where the introduced amount of the tetraethyl silicate was the same as that in Example 10. A resulting mixture was purged with nitrogen, heated to 550° C., and then calcined in an air atmosphere for 4 hours to obtain a fixed bed catalyst used for coupling conversion of naphtha and CO2 to produce benzene, toluene and p-xylene, named as FXNCC-7.
Then, the temperature was adjusted to a reaction temperature of 550° C. in a nitrogen atmosphere. A raw material naphtha was fed by a micro-feed pump, and the flow of CO2 was controlled by a mass flow meter. The mass ratio of the raw material CO2 to the naphtha was 0.8:1, the weight hourly space velocity of the CO2 was 0.8 h−1, the weight hourly space velocity of the naphtha was 1.0 h−1, and the reaction pressure was 0.1 MPa. Reaction products were analyzed by on-line Agilent7890 gas chromatography, and sampling was carried out for analysis when a reaction was carried out for 30 minutes. Reaction results are shown in Table 8.
A catalyst used for coupling conversion of naphtha and CO2 to produce benzene, toluene and p-xylene was prepared on-line in a micro-fixed bed reactor. Conditions for on-line preparation of the catalyst are as follows. 5 g of the FX-[Zn]HZSM-5-R catalyst prepared in Example 8 was loaded into a fixed bed reactor, treated with nitrogen at 50 ml/min at 550° C. for 1 hour, and then cooled to 300° C. in a nitrogen atmosphere. In the nitrogen atmosphere (controlled by a mass flow meter, 100 mL/min), tetraethyl silicate was pumped into the reactor at a weight hourly space velocity of 0.2 h−1 at normal pressure. After feeding for 60 minutes, the feeding was stopped, where the introduced amount of the tetraethyl silicate was the same as that in Example 10. A resulting mixture was purged with nitrogen, heated to 550° C., and then calcined in an air atmosphere for 4 hours to obtain a fixed bed catalyst used for coupling conversion of naphtha and CO2 to produce benzene, toluene and p-xylene, named as FXNCC-8.
Then, the temperature was adjusted to a reaction temperature of 550° C. in a nitrogen atmosphere. A raw material naphtha was fed by a micro-feed pump, and the flow of CO2 was controlled by a mass flow meter. The mass ratio of the raw material CO2 to the naphtha was 0.8:1, the weight hourly space velocity of the CO2 was 0.8 h−1, the weight hourly space velocity of the naphtha was 1.0 h−1, and the reaction pressure was 0.1 MPa. Reaction products were analyzed by on-line Agilent7890 gas chromatography, and sampling was carried out for analysis when a reaction was carried out for 30 minutes. Reaction results are shown in Table 9.
Compared with the selectivity of BTPX in Example 10, the HZSM-5 molecular sieve obtained by metal modification using a high temperature hydrothermal method can achieve higher selectivity of BTPX than that obtained by metal modification using a room temperature impregnation method.
A catalyst used for coupling conversion of naphtha and CO2 to produce benzene, toluene and p-xylene was prepared on-line in a micro-fixed bed reactor. Conditions for on-line preparation of the catalyst are as follows. 5 g of a 40- to 60-mesh HZSM-5 molecular sieve catalyst was loaded into a fixed bed reactor, treated with nitrogen at 50 ml/min at 550° C. for 1 hour, and then cooled to 300° C. in a nitrogen atmosphere. In the nitrogen atmosphere (controlled by a mass flow meter, 100 mL/min), tetraethyl silicate was pumped into the reactor at a weight hourly space velocity of 0.2 h−1 at normal pressure. After feeding for 60 minutes, the feeding was stopped, where the introduced amount of the tetraethyl silicate was the same as that in Example 10. A resulting mixture was purged with nitrogen, heated to 550° C., and then calcined in an air atmosphere for 4 hours to obtain a fixed bed catalyst used for coupling conversion of naphtha and CO2 to produce benzene, toluene and p-xylene, named as FXNCC-9.
Then, the temperature was adjusted to a reaction temperature of 550° C. in a nitrogen atmosphere. A raw material naphtha was fed by a micro-feed pump, and the flow of CO2 was controlled by a mass flow meter. The mass ratio of the raw material CO2 to the naphtha was 0.8:1, the weight hourly space velocity of the CO2 was 0.8 h−1, the weight hourly space velocity of the naphtha was 1.0 h−1, and the reaction pressure was 0.1 MPa. Reaction products were analyzed by on-line Agilent7890 gas chromatography, and sampling was carried out for analysis when a reaction was carried out for 30 minutes. Reaction results are shown in Table 9-1.
5 g of the FXNCC-9 catalyst prepared in Example 19 was placed in a 10 wt % lanthanum nitrate aqueous solution, where the solid-liquid ratio of the HZSM-5 zeolite molecular sieve used in the FXNCC-9 catalyst to the lanthanum nitrate aqueous solution was the same as that in Example 3. The catalyst was impregnated at 90° C. for 4 hours, drained, dried in an air atmosphere at 120° C. for 4 hours, and then calcined in an air atmosphere at 550° C. for 4 hours to obtain a catalyst sample, recorded as FXNCC-10.
The reaction performance of the catalyst used for coupling conversion of naphtha and CO2 was evaluated in a micro-fixed bed reactor. Evaluation conditions are as follows. 5 g of the FXNCC-10 catalyst molded sample (40-60 mesh) was loaded into a fixed bed reactor, and the temperature was raised to a reaction temperature of 550° C. in a nitrogen atmosphere. A raw material naphtha was fed by a micro-feed pump, and the flow of CO2 was controlled by a mass flow meter. The mass ratio of the raw material CO2 to the naphtha was 0.8:1, the weight hourly space velocity of the CO2 was 0.8 h−1, the weight hourly space velocity of the naphtha was 1.0 h−1, and the reaction pressure was 0.1 MPa. Reaction products were analyzed by on-line Agilent7890 gas chromatography, and sampling was carried out for analysis when a reaction was carried out for 30 minutes. Reaction results are shown in Table 10.
By comparing with Example 12, the catalyst in this example achieves lower selectivity of BTPX and lower selectivity of p-xylene in xylene. The results indicate that when La is used for metal modification, a molecular sieve obtained by carrying out metal modification first and then carrying out silanization modification can achieve higher selectivity of BTPX and higher selectivity of p-xylene in xylene compared with a molecular sieve obtained by carrying out silanization modification first and then carrying out metal modification.
A catalyst used for conversion of naphtha to produce benzene, toluene and p-xylene was prepared on-line in a micro-fixed bed reactor. Conditions for on-line preparation of the catalyst are as follows. 5 g of the FX-[Zn]HZSM-5 catalyst prepared in Example 1 was loaded into a fixed bed reactor, treated with nitrogen at 50 ml/min at 550° C. for 1 hour, and then cooled to 300° C. in a nitrogen atmosphere. In the nitrogen atmosphere (controlled by a mass flow meter, 100 mL/min), tetraethyl silicate was pumped into the reactor at a weight hourly space velocity of 0.2 h−1 at normal pressure. After feeding for 60 minutes, the feeding was stopped, where the introduced amount of the tetraethyl silicate was the same as that in Example 10. A resulting mixture was purged with nitrogen, heated to 550° C., and then calcined in an air atmosphere for 4 hours to obtain a fixed bed catalyst used for conversion of naphtha to produce benzene, toluene and p-xylene, named as FXNCC-1.
Then, the temperature was adjusted to a reaction temperature of 550° C. in a nitrogen atmosphere. A raw material naphtha was fed by a micro-feed pump, and the flow of N2 was controlled by a mass flow meter. The mass ratio of the raw material N2 to the naphtha was 0.51:1 (namely, an equivalent molar amount of N2 was used in this example to replace the CO2 in Example 10), the weight hourly space velocity of the naphtha was 1.0 h−1, the weight hourly space velocity of the N2 was 0.51 h−1, and the reaction pressure was 0.1 MPa. Reaction products were analyzed by on-line Agilent7890 gas chromatography, and sampling was carried out for analysis when a reaction was carried out for 30 minutes. Reaction results are shown in Table 11.
The N2 is used as a diluent in Example 21, and the CO2 is used as a raw material for reacting with the naphtha in Example 10, which can be seen by comparing the selectivity of aromatic hydrocarbons and the selectivity of BTPX in Examples 10 and 21. Specifically, the selectivity of aromatic hydrocarbons and the selectivity of BTPX in Example 10 are obviously higher than the selectivity of aromatic hydrocarbons in Example 21.
A catalyst used for coupling conversion of naphtha and CO2 to produce benzene, toluene and p-xylene was prepared on-line in a micro-fixed bed reactor. Conditions for on-line preparation of the catalyst are as follows. 5 g of the FX-[Zn]HZSM-5 catalyst prepared in Example 1 was loaded into a fixed bed reactor, treated with nitrogen at 50 ml/min at 550° C. for 1 hour, and then cooled to 300° C. in a nitrogen atmosphere. In the nitrogen atmosphere (controlled by a mass flow meter, 100 mL/min), tetraethyl silicate was pumped into the reactor at a weight hourly space velocity of 0.2 h−1 at normal pressure. After feeding for 60 minutes, the feeding was stopped, where the introduced amount of the tetraethyl silicate was the same as that in Example 10. A resulting mixture was purged with nitrogen, heated to 550° C., and then calcined in an air atmosphere for 4 hours. Then, the mixture was heated to 900° C. in the nitrogen atmosphere, and treated for 1 hour in a 100% water vapor atmosphere (WHSV of water was 2 h−1) to obtain a fixed bed catalyst used for coupling conversion of naphtha and CO2 to produce benzene, toluene and p-xylene, named as FXNCC-11.
Then, the temperature was adjusted to a reaction temperature of 550° C. in a nitrogen atmosphere. A raw material naphtha was fed by a micro-feed pump, and the flow of CO2 was controlled by a mass flow meter. The mass ratio of the raw material CO2 to the naphtha was 0.8:1, the weight hourly space velocity of the naphtha was 1.0 h−1, and the reaction pressure was 0.1 MPa. Reaction products were analyzed by on-line Agilent7890 gas chromatography, and sampling was carried out for analysis when a reaction was carried out for 30 minutes. Reaction results are shown in Table 12.
A catalyst used for coupling conversion of naphtha and CO2 to produce benzene, toluene and p-xylene was prepared on-line in a micro-fixed bed reactor. Conditions for on-line preparation of the catalyst are as follows. 5 g of the FX-[Zn]HZSM-5-R catalyst prepared in Example 8 was loaded into a fixed bed reactor, treated with nitrogen at 50 ml/min at 550° C. for 1 hour, and then cooled to 300° C. in a nitrogen atmosphere. In the nitrogen atmosphere (controlled by a mass flow meter, 100 mL/min), tetraethyl silicate was pumped into the reactor at a weight hourly space velocity of 0.2 h−1 at normal pressure. After feeding for 60 minutes, the feeding was stopped, where the introduced amount of the tetraethyl silicate was the same as that in Example 10. A resulting mixture was purged with nitrogen, heated to 550° C., and then calcined in an air atmosphere for 4 hours. Then, the mixture was heated to 900° C. in a nitrogen atmosphere, and treated for 1 hour in a 100% water vapor atmosphere (WHSV of water was 2 h−1) to obtain a fixed bed catalyst used for coupling conversion of naphtha and CO2 to produce benzene, toluene and p-xylene, named as FXNCC-12.
Then, the temperature was adjusted to a reaction temperature of 550° C. in a nitrogen atmosphere. A raw material naphtha was fed by a micro-feed pump, and the flow of CO2 was controlled by a mass flow meter. The mass ratio of the raw material CO2 to the naphtha was 0.8:1, the weight hourly space velocity of the naphtha was 1.0 h−1, and the reaction pressure was 0.1 MPa. Reaction products were analyzed by on-line Agilent7890 gas chromatography, and sampling was carried out for analysis when a reaction was carried out for 30 minutes. Reaction results are shown in Table 13.
By comparing Examples 22 and 23, it can be seen that the catalyst obtained after hydrothermal treatment in Example 22 has obviously higher selectivity of aromatic hydrocarbons and higher selectivity of BTPX than the catalyst obtained after hydrothermal treatment in Example 23. Therefore, the hydrothermal stability of the metal-modified HZSM-5 prepared by a high temperature hydrothermal method is obviously better than that of the metal-modified HZSM-5 prepared by a room temperature impregnation method.
A catalyst FXNCC-1 was prepared by the method in Example 10.
Then, the temperature was adjusted to a reaction temperature of 550° C. in a nitrogen atmosphere. A raw material naphtha was fed by a micro-feed pump, and the flow of CO2 was controlled by a mass flow meter. The mass ratio of the raw material CO2 to the naphtha was 1:1, the weight hourly space velocity of the CO2 was 5 h−1, the weight hourly space velocity of the naphtha was 5 h−1, and the reaction pressure was 1 MPa. Reaction products were analyzed by on-line Agilent7890 gas chromatography, and sampling was carried out for analysis when a reaction was carried out for 30 minutes. Reaction results are shown in Table 14.
A catalyst FXNCC-1 was prepared by the method in Example 10.
Then, the temperature was adjusted to a reaction temperature of 550° C. in a nitrogen atmosphere. A raw material naphtha was fed by a micro-feed pump, and the flow of CO2 was controlled by a mass flow meter. The mass ratio of the raw material CO2 to the naphtha was 1:1, the weight hourly space velocity of the CO2 was 0.1 h−1, the weight hourly space velocity of the naphtha was 0.1 h−1, and the reaction pressure was 0.1 MPa. Reaction products were analyzed by on-line Agilent7890 gas chromatography, and sampling was carried out for analysis when a reaction was carried out for 30 minutes. Reaction results are shown in Table 15.
100 g of an HZSM-5 zeolite molecular sieve (Nankai Catalyst Factory, Si/Al=15) was placed in a 30 wt % zinc nitrate aqueous solution, where the mass ratio (namely solid-liquid ratio) of the HZSM-5 zeolite molecular sieve to the zinc nitrate aqueous solution was 1/10. The molecular sieve was impregnated at 80° C. for 4 hours, drained, dried in an air atmosphere at 120° C. for 4 hours, and then calcined in an air atmosphere at 550° C. for 4 hours to obtain a [Zn]HZSM-5 molecular sieve sample. Then, the sample was subjected to pressing molding, crushed and sieved to obtain molded molecular sieve particles with a particle size of 40-60 mesh, recorded as FX-[Zn]HZSM-5-B.
A catalyst used for coupling conversion of naphtha and CO2 to produce benzene, toluene and p-xylene was prepared on-line in a micro-fixed bed reactor. Conditions for on-line preparation of the catalyst are as follows. 5 g of the FX-[Zn]HZSM-5-B catalyst prepared in Example 26 was loaded into a fixed bed reactor, treated with nitrogen at 50 ml/min at 550° C. for 1 hour, and then cooled to 300° C. in a nitrogen atmosphere. In the nitrogen atmosphere (controlled by a mass flow meter, 100 mL/min), tetraethyl silicate was pumped into the reactor at a weight hourly space velocity of 0.2 h−1 at normal pressure. After feeding for 60 minutes, the feeding was stopped, where the introduced amount of the tetraethyl silicate was 0.2 g/g the catalyst. A resulting mixture was purged with nitrogen, heated to 550° C., and then calcined in an air atmosphere for 4 hours to obtain a fixed bed catalyst used for coupling conversion of naphtha and CO2 to produce benzene, toluene and p-xylene, named as FXNCC-13.
Then, the temperature was adjusted to a reaction temperature of 550° C. in a nitrogen atmosphere. A raw material naphtha was fed by a micro-feed pump, and the flow of CO2 was controlled by a mass flow meter. The mass ratio of the raw material CO2 to the naphtha was 0.8:1, the weight hourly space velocity of the CO2 was 0.8 h−1, the weight hourly space velocity of the naphtha was 1.0 h−1, and the reaction pressure was 0.1 MPa. Reaction products were analyzed by on-line Agilent7890 gas chromatography, and sampling was carried out for analysis when a reaction was carried out for 30 minutes. Reaction results are shown in Table 16.
A catalyst FXNCC-1 was prepared by the method in Example 10.
Then, the temperature was adjusted to a reaction temperature of 550° C. in a nitrogen atmosphere. A raw material naphtha was fed by a micro-feed pump, and the flow of CO2 was controlled by a mass flow meter. The mass ratio of the raw material CO2 to the naphtha was 0.8:0.27, the weight hourly space velocity of the CO2 was 0.8 h−1, the weight hourly space velocity of the naphtha was 0.27 h−1, and the reaction pressure was 0.1 MPa. Reaction products were analyzed by on-line Agilent7890 gas chromatography, and sampling was carried out for analysis when a reaction was carried out for 30 minutes. Reaction results are shown in Table 17.
A catalyst used for coupling conversion of naphtha and CO2 to produce benzene, toluene and p-xylene was prepared on-line in a micro-fixed bed reactor. Conditions for on-line preparation of the catalyst are as follows. 5 g of the FX-[Zn]HZSM-5 catalyst prepared in Example 1 was loaded into a fixed bed reactor, treated with nitrogen at 50 ml/min at 550° C. for 1 hour, and then cooled to 300° C. in a nitrogen atmosphere. Then, a vapor atomic layer deposition method was used to carry out modification with a silanization reagent, specifically including the following steps: (1) introducing nitrogen (controlled by a mass flow meter, 200 mL/min) into a saturated flask filled with tetraethyl silicate (temperature 10° C.), then introducing the same into a reactor, namely introducing the nitrogen carrying the tetraethyl silicate into the reactor, and after feeding for 5 minutes, stopping the feeding; (2) carrying out purging with nitrogen, and raising the temperature to 550° C., followed by calcination in an air atmosphere for 1 hour; and (3) repeating steps (1) and (2) for 5 times to obtain a fixed bed catalyst used for coupling conversion of naphtha and CO2 to produce benzene, toluene and p-xylene, named as FXNCC-14, where the amount of the tetraethyl silicate introduced for 6 times was equivalent to the amount introduced for one time in Example 10.
Then, the temperature was adjusted to a reaction temperature of 550° C. in a nitrogen atmosphere. A raw material naphtha was fed by a micro-feed pump, and the flow of CO2 was controlled by a mass flow meter. The mass ratio of the raw material CO2 to the naphtha was 0.8:1, the weight hourly space velocity of the naphtha was 1.0 h−1, and the reaction pressure was 0.1 MPa. Reaction products were analyzed by on-line Agilent7890 gas chromatography, and sampling was carried out for analysis when a reaction was carried out for 30 minutes. Reaction results are shown in Table 18.
In addition to the naphtha used in the above examples, any naphtha selected from hydrocracked naphtha, catalytic cracked naphtha, raffinate oil and topped oil or any mixture thereof may also be used in the present application.
The above descriptions are only several examples of the present application, and are not intended to limit the present application in any way. Although the present application is disclosed above through preferred examples, the examples are not intended to limit the present application. For any skilled person familiar with the art, various changes or modifications made by using the technical contents disclosed above without departing from the scope of technical schemes of the present application are considered as equivalent examples, which fall within the scope of the technical schemes.
| Number | Date | Country | Kind |
|---|---|---|---|
| 202111124097.3 | Sep 2021 | CN | national |
This application is the national phase entry of International Application No. PCT/CN2021/133888, filed on Nov. 29, 2021, which is based upon and claims priority to Chinese Patent Application No. 202111124097.3, filed on Sep. 24, 2021, the entire contents of which are incorporated herein by reference.
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/CN2021/133888 | 11/29/2021 | WO |
