COMPOSITE ZSM-5 MOLECULAR SIEVE, PREPARATION METHOD THEREFOR, CATALYST AND USE THEREOF
20230132229 · 2023-04-27
Assignee
- China Energy Investment Corporation Limited (Beijing, CN)
- National Institute of Clean-and-Low-Carbon Energy (Beijing, CN)
Inventors
Cpc classification
C07C2529/40
CHEMISTRY; METALLURGY
B01J37/0236
PERFORMING OPERATIONS; TRANSPORTING
Y02P20/52
GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
B01J37/009
PERFORMING OPERATIONS; TRANSPORTING
B01J37/0018
PERFORMING OPERATIONS; TRANSPORTING
International classification
B01J29/40
PERFORMING OPERATIONS; TRANSPORTING
B01J37/00
PERFORMING OPERATIONS; TRANSPORTING
B01J37/02
PERFORMING OPERATIONS; TRANSPORTING
B01J37/03
PERFORMING OPERATIONS; TRANSPORTING
Abstract
The present invention relates to the field of alkylation catalysts, and disclosed are a composite ZSM-5 molecular sieve, a preparation method therefor, a catalyst and an application thereof. A single crystal of the composite ZSM-5 molecular sieve comprises a main crystal and a twin crystal; the main crystal and the twin crystal are both ZSM-5 crystals; a crystal plane [010] of the main crystal is covered by a crystal plane [100] of the twin crystal; and the ratio of the number of sinusoidal pore openings to the number of straight pore openings on the outer surface of the single crystal of the composite ZSM-5 molecular sieve is (0.7-10:1), and the molar ratio Y1 of an Si element to an Al element within 10 nm of the surface is (300-2000):1. The single crystal of the composite ZSM-5 molecular sieve of the present invention has a large ratio of the number of sinusoidal pore openings to the number of straight pore openings, and is aluminum-poor on the surface and aluminum-rich on the inside. When applied to the toluene methanol alkylation reaction to prepare p-xylene, the selectivity of p-xylene may be greatly improved.
Claims
1-18. (canceled)
19. A composite ZSM-5 molecular sieve whose a single crystal comprises a main crystal and a twin crystal; wherein the main crystal and the twin crystal are both ZSM-5 crystals; a crystal plane [010] of the main crystal is covered by a crystal plane [100] of the twin crystal; the ratio of the number of sinusoidal pore openings to the number of straight pore openings on the external surface of the single crystal of the composite ZSM-5 molecular sieve is (0.7-10:1); the molar ratio Y.sub.1 of Si element to Al element within 10 nm of the surface of the composite ZSM-5 molecular sieve is (300-2,000):1.
20. The composite ZSM-5 molecular sieve of claim 19, wherein the ratio of the number of sinusoidal pore openings to the number of straight pore openings on the external surface of the single crystal of the composite ZSM-5 molecular sieve is (0.9-3.2):1.
21. The composite ZSM-5 molecular sieve of claim 19, wherein the molar ratio Y.sub.1 of Si element to Al element within 10 nm of the surface of the composite ZSM-5 molecular sieve is (500-1,200): 1.
22. The composite ZSM-5 molecular sieve of claim 19, wherein the molar ratio Y.sub.2 of Si element to Al element of the composite ZSM-5 molecular sieve as a whole is (20-600):1.
23. The composite ZSM-5 molecular sieve of claim 19, wherein a single crystal of the composite ZSM-5 molecular sieve has a length of 10-50 μm, a height of 1-20 μm and a width of 1-20 μm; and a single crystal of the composite ZSM-5 molecular sieve has a specific surface area of 200-600 m.sup.2/g.
24. A method for preparing a composite ZSM-5 molecular sieve comprising: (1) mixing a silicon source and an aluminum source in the presence of water, a first templating agent and a second templating agent, adjusting the pH to be within a range of 11-13.5, and then performing crystallization; (2) subjecting the crystallized product to a solid-liquid separation, and calcining the obtained solid phase to prepare the composite ZSM-5 molecular sieve; wherein the first templating agent is at least one selected from the group consisting of tetraethylammonium hydroxide, tetrapropylammonium hydroxide, tetrapropylammonium bromide and tetrabutylammonium hydroxide, the second templating agent is at least one selected from the group consisting of ethylenediamine, n-butylamine, hexamethylenediamine, ethylamine, ethanol and ethanolamine; and the used amount of the first templating agent to the second templating agent in a molar ratio is 1:(1-30).
25. The method of claim 24, wherein a molar ratio of the used amount of the first templating agent to the second templating agent is 1:(3-20).
26. The method of claim 24, wherein the pH in step (1) is adjusted to 11.2-13.
27. The method of claim 24, wherein a molar ratio of the used amount of the silicon source, the aluminum source, the first templating agent, the second templating agent and water is 100:(0.08-2.5):(0.5-6):(0.5-60):(100-4,000); wherein the silicon source is calculated in terms of SiO.sub.2, the aluminum source is calculated in terms of Al.sub.2O.sub.3.
28. The method of claim 24, wherein the crystallization conditions in step (1) comprise a temperature of 120-250° C. and a time of 12-72 h; the calcination conditions in step (2) comprise a temperature of 500-700° C., and a time of 1-24 h.
29. The method of claim 24, wherein the solid phase obtained from the solid-liquid separation is subjected to drying prior to calcining.
30. The composite ZSM-5 molecular sieve produced with the preparation method of claim 24.
31. A catalyst comprising the composite ZSM-5 molecular sieve of claim 19.
32. A method of using the composite ZSM-5 molecular sieve of claim 19 in the alkylation reaction of toluene methanol to prepare p-xylene.
33. The composite ZSM-5 molecular sieve of claim 22, wherein the molar ratio Y.sub.2 of Si element to Al element of the composite ZSM-5 molecular sieve as a whole is (50-300):1.
34. The method of claim 27, wherein a molar ratio of the used amount of the silicon source, the aluminum source, the first templating agent, the second templating agent and water is 100:(0.4-2):(1-6):(3-30):(500-4,000).
35. The method of claim 28, wherein the crystallization conditions in step (1) comprise a temperature of 150-180° C. and a time of 24-60 h; the calcination conditions in step (2) comprise a temperature of 500-700° C., and a time of 4-12 h.
36. The method of claim 29, wherein the drying conditions comprise a temperature of 90-200° C. and a time of 2-12 h.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0018]
[0019]
[0020]
[0021]
[0022]
[0023]
[0024]
DETAILED DESCRIPTION
[0025] The terminals and any value of the ranges disclosed herein are not limited to the precise ranges or values, such ranges or values shall be comprehended as comprising the values adjacent to the ranges or values. As for numerical ranges, the endpoint values of the various ranges, the endpoint values and the individual point value of the various ranges, and the individual point values may be combined with one another to produce one or more new numerical ranges, which should be deemed have been specifically disclosed herein.
[0026] In a first aspect, the present disclosure provides a composite ZSM-5 molecular sieve, as shown in
[0027] According to parameters published by the International Zeolite Association (IZA), there is a straight pore opening for each area of 20.090 angstrom×13.142 angstrom on a crystal plane [010] of the ZSM-5 molecular sieve, and there is a sinusoidal pore opening for each area of 19.7380 angstrom×13.1420 angstrom. The dimensions of each crystal plane of each molecular sieve crystal are obtained by the SEM spectrogram, and the ratio of the number of sinusoidal pore openings to the number of straight pore openings on the external surface of the single crystal of the composite ZSM-5 molecular sieve according to the present disclosure is obtained by calculating an area of the crystal plane. Preferably, the ratio of the number of sinusoidal pore openings to the number of straight pore openings on the external surface of the single crystal of the composite ZSM-5 molecular sieve is (0.9-3.2):1.
[0028] According to the present disclosure, it is preferred that a single crystal of the composite ZSM-5 molecular sieve has a length of 10-50 μm, a height of 1-20 μm and a width of 1-20 μm; and a single crystal of the composite ZSM-5 molecular sieve has a specific surface area of 200-600 m.sup.2/g. As shown in
[0029] In the present disclosure, the content of Si element and Al element within 10 nm of the surface of the composite ZSM-5 molecular sieve is scanned by using the X-ray Photoelectron Spectroscopy (XPS) technique, and the molar ratio Y.sub.1 is obtained by calculating. Y.sub.1 is preferably (300-1,500):1, more preferably (500-1,200):1. In the present disclosure, within 10 nm of the surface of the composite ZSM-5 molecular sieve refers to the portion having a thickness within 10 nm from the surface of the composite ZSM-5 molecular sieve.
[0030] According to the present disclosure, the molar ratio (hereinafter referred to Y.sub.2) of Si element to Al element of the composite ZSM-5 molecular sieve as a whole is preferably (20-600):1, more preferably (50-300):1. After exposing the inside of the molecular sieve by crushing the particles of the composite ZSM-5 molecular sieve, the contents of Si element and Al element of the composite ZSM-5 molecular sieve as a whole are calculated by using the XPS technique, the molar ratio Y.sub.2 is obtained by calculating.
[0031] The composite ZSM-5 molecular sieve provided by the present disclosure is aluminum-poor on the surface and aluminum-rich on the inside; when the composite ZSM-5 molecular sieve is used for preparing p-xylene, the generated p-xylene will not be isomerized on the surface of the composite ZSM-5 molecular sieve, such that the p-xylene selectivity can be improved.
[0032] In a second aspect, the present disclosure provides a method for preparing a composite ZSM-5 molecular sieve comprising:
[0033] (1) mixing a silicon source and an aluminum source in the presence of water, a first templating agent and a second templating agent, adjusting the pH to be within a range of 11-13.5, and then performing crystallization;
[0034] (2) subjecting the crystallized product to a solid-liquid separation, and calcining the obtained solid phase to prepare the composite ZSM-5 molecular sieve;
[0035] wherein the first templating agent is at least one selected from the group consisting of tetraethylammonium hydroxide, tetrapropylammonium hydroxide, tetrapropylammonium bromide and tetrabutylammonium hydroxide, the second templating agent is at least one selected from the group consisting of ethylenediamine, n-butylamine, hexamethylenediamine, ethylamine, ethanol and ethanolamine; and the used amount of the first templating agent to the second templating agent in a molar ratio is 1:(1-30).
[0036] The inventors of the present disclosure have discovered in researches that by selecting the specific kinds of the first templating agent and the second templating agent, and controlling a ratio of the used amount of the first templating agent to the second templating agent within a certain range, the composite ZSM-5 molecular sieve crystals comprising a main crystal and a twin crystal can be obtained, and a crystal plane [010] of the main crystal is covered by a crystal plane [100] of the twin crystal, such that the ratio of the number of sinusoidal pore openings to the number of straight pore openings on the external surface of the single crystal of the composite ZSM-5 molecular sieve is high, and the molar ratio of Si element to Al element within 10 nm of the surface of the composite ZSM-5 molecular sieve is large. A molar ratio of the used amount of the first templating agent to the second templating agent is preferably 1:(3-20), more preferably 1:(5-15).
[0037] Preferably, the pH in step (1) is adjusted to 11.2-13. The inventors of the present disclosure have discovered in researches that by controlling pH to be within the above range, the obtained composite ZSM-5 molecular sieve can further improve the p-xylene selectivity when it is used in a reaction for producing para-xylene.
[0038] In the present disclosure, the pH may be adjusted by means of the existing technical means, such as adjusting the pH by adding an alkaline substance, the alkaline substance is preferably sodium hydroxide and/or potassium hydroxide.
[0039] In the present disclosure, the silicon source may be at least one selected from the group consisting of an organic silicone grease, a silica sol and a solid silica gel. The organic silicone grease is preferably ethyl orthosilicate and/or methyl orthosilicate. The aluminum source may be at least one selected from the group consisting of sodium metaaluminate, sodium aluminate, aluminum nitrate, aluminum sulfate and aluminum isopropoxide.
[0040] Preferably, a molar ratio of the used amount of the silicon source, the aluminum source, the first templating agent, the second templating agent and water is 100:(0.08-2.5):(0.5-6):(0.5-60):(100-4,000); wherein the silicon source is calculated in terms of SiO.sub.2, the aluminum source is calculated in terms of Al.sub.2O.sub.3. Further preferably, the silicon source, the aluminum source, the first templating agent, the second templating agent and water are used in a molar ratio of 100:(0.4-2):(1-6):(3-30):(500-4,000). In the present disclosure, the used amount of water refers to the amount of water in the overall system, when the silicon source, the aluminum source, the first templating agent or the second templating agent are added in the form of an aqueous solution, the used amount of water comprises the solvent water in the aqueous solution.
[0041] The conditions for carrying out the crystallization in step (1) are not particularly defined in the present disclosure, in order to produce a favorable crystallization effect. The crystallization conditions in step (1) preferably comprise a temperature of 120-250° C. and a time of 12-72 h, more preferably a temperature of 150-180° C. and a time of 24-60 h.
[0042] The conditions for carrying out the calcination in step (2) are not particularly defined in the present disclosure, in order to produce a favorable calcination effect. The calcination conditions preferably comprise a temperature of 500-700° C., and a time of 1-24 h, more preferably 4-12 h.
[0043] According to a preferred embodiment of the present disclosure, the solid phase obtained from the solid-liquid separation is subjected to drying prior to calcining.
[0044] Preferably, the drying conditions preferably comprise a temperature of 90-200° C. and a time of 2-12 h.
[0045] In a third aspect, the present disclosure provides a composite ZSM-5 molecular sieve produced with the preparation method of the present disclosure.
[0046] Wherein a single crystal of the composite ZSM-5 molecular sieve comprises a main crystal and a twin crystal; wherein the main crystal and the twin crystal are both ZSM-5 crystals; a crystal plane [010] of the main crystal is covered by a crystal plane [100] of the twin crystal; the ratio of the number of sinusoidal pore openings to the number of straight pore openings on the external surface of the single crystal of the composite ZSM-5 molecular sieve is (0.7-10:1); the molar ratio Y.sub.1 of Si element to Al element within 10 nm of the surface of the composite ZSM-5 molecular sieve is (300-2,000):1.
[0047] Preferably, the ratio of the number of sinusoidal pore openings to the number of straight pore openings on the external surface of the single crystal of the composite ZSM-5 molecular sieve is (0.9-3.2):1.
[0048] Preferably, the molar ratio Y.sub.1 of Si element to Al element within 10 nm of the surface of the composite ZSM-5 molecular sieve is (500-1,200): 1.
[0049] Preferably, the molar ratio Y.sub.2 of Si element to Al element of the composite ZSM-5 molecular sieve as a whole is (20-600):1, preferably (50-300): 1.
[0050] In a fourth aspect, the present disclosure provides a catalyst comprising the composite ZSM-5 molecular sieve of the present disclosure. According to the present disclosure, the catalyst comprises the composite ZSM-5 molecular sieve as an active component. Besides the composite ZSM-5 molecular sieve, the catalyst may further comprise the conventional catalyst ingredients such as a modifying agent, a pore-enlarging agent and a binder, and may have a conventional structure and shape of the catalysts in the art, such that the catalysts are applicable to the different types of reactors. The content of said composite ZSM-5 molecular sieve may be 40-90 wt % of the total amount of the catalyst.
[0051] In a fifth aspect, the present disclosure provides a use of the composite ZSM-5 molecular sieve of the present disclosure or the catalyst of the present disclosure in the alkylation reaction of toluene methanol to prepare p-xylene.
[0052] According to the present disclosure, the catalyst and the composite ZSM-5 molecular sieve have substantially equivalent catalytic effect to the alkylation reaction of toluene methanol for preparing p-xylene.
[0053] When compared with the conventionally modified ZSM-5 molecular sieves, the composite ZSM-5 molecular sieve provided by the present disclosure has the following advantages:
[0054] (1) The composite ZSM-5 molecular sieve of the present disclosure utilizes the sinusoidal pore channels having a large diffusion resistance to the xylene molecules to accomplish the shape-selective function of said molecular sieve to a large extent, prevents the straight pore channels having poor shape-selective effect from participating the shape-selective and catalytic process, such that the selectivity of said molecular sieve in regard to p-xylene can be greatly improved.
[0055] (2) In contrast to the modified ZSM-5 molecular sieve, the composite ZSM-5 molecular sieve of the present disclosure is synthesized and prepared directly by a one-step process, there is not a process of modifying the molecular sieve, thus the number of acid centers is not affected by the modification process, and the original activity of the molecular sieve is retained by 100%. In addition, there is not the circumstance with respect to running off of the modifying agent and degraded shape-selective property of the molecular sieve during the reaction process.
[0056] (3) The molecular sieve obtained by the present disclosure is aluminum-poor on the external surface, when the molecular sieve is used for the catalytic production of p-xylene, the generated p-xylene is not isomerized on a surface of the composite ZSM-5 molecular sieve, such that its p-xylene selectivity can be further improved.
[0057] The present disclosure will be described below in detail with reference to examples. In the following examples, the SEM spectrograms were measured by the spherical-aberration correction scanning electron microscopy (ac-SEM) (Nova NanoSEM 450, commercially available from FEI).
[0058] According to parameters published by the International Zeolite Association (IZA), there was a straight pore opening for each area of 20.090 angstrom×13.142 angstrom on a crystal plane [010] of the ZSM-5 molecular sieve, and there was a sinusoidal pore opening for each area of 19.7380 angstrom×13.1420 angstrom. The dimensions of each crystal plane of each molecular sieve crystal were obtained by the SEM spectrogram, and the ratio of the number of sinusoidal pore openings to the number of straight pore openings on the external surface of the single crystal of the composite ZSM-5 molecular sieve according to the present disclosure was obtained by calculating an area of the crystal plane.
[0059] The Elemental analysis of the composite ZSM-5 molecular sieve was performed by using the X-ray photoelectron spectroscopy (ESCALAB 250Xi, commercially available from Thermo-Fisher).
[0060] 1) The molar ratio Y.sub.1 was obtained by scanning the elements within 10 nm of the surface of the composite ZSM-5 molecular sieve by using the X-ray Photoelectron Spectroscopy (XPS) technique;
[0061] 2) After exposing the inside of the molecular sieve by crushing the particles of the composite ZSM-5 molecular sieve, the molar ratio Y.sub.2 was obtained by using the X-ray Photoelectron Spectroscopy (XPS) technique.
[0062] The length, height and width of a single crystal of the composite ZSM-5 molecular sieve were obtained by the spherical-aberration correction scanning electron microscopy (ac-SEM); the specific surface area was measured by N.sub.2 physical adsorption after pretreatment of the test sample at 350° C., and the specific surface area was calculated by using the Brunauer, Emmett and Teller (BET) model.
Example 1
[0063] (1) 60 g of silica sol solution (30 wt %) was mixed with sodium metaaluminate, tetrapropylammonium bromide, n-butylamine and water, wherein the used amounts of said raw materials satisfied SiO.sub.2:Al.sub.2O.sub.3:tetrapropylammonium bromide:n-butylamine:water=100:0.67:4.5:35.3:3,333 (molar ratio), sodium hydroxide was added to adjust the pH to 12, then stirred uniformly for 30 minutes, the mixture was poured into a rotary self-pressurization crystallization kettle to carry out crystallization at 180° C. for 48 h;
[0064] (2) the crystallized sample of step (1) was filtered and washed with deionized water to neutral, then placed in an oven for drying at 120° C. for 2 h; the dried solid was placed in a muffle furnace, the temperature was raised from room temperature (25° C.) to 550° C. at a temperature rise rate of 1° C./min under a flowing air atmosphere, the dried solid was then roasted at a constant temperature of 550° C. for 5 h, and subsequently cooled naturally to room temperature to prepare the composite ZSM-5 molecular sieve M1. The composite ZSM-5 molecular sieve had a length of 50 μm, a height of 20 μm, a width of 20 μm, and a specific surface area of 420 m.sup.2/g.
[0065] As characterized by the SEM spectrogram (as shown in
[0066] The composite ZSM-5 molecular sieve was subjected to the elemental analysis, the results were shown in
Example 2
[0067] (1) 18 g of solid silica gel powder (with a silica content more than 99 wt %) was mixed with aluminum sulfate, aqueous solution of tetrapropylammonium hydroxide (25 wt %), hexamethylenediamine and water, wherein the used amounts of said raw materials satisfied SiO.sub.2:Al.sub.2O.sub.3:tetrapropylammonium hydroxide:hexamethylenediamine:water=100:0.67:3:30:3,000 (molar ratio), potassium hydroxide was added to adjust the pH to 12.5, then stirred uniformly for 30 minutes, the mixture was poured into a rotary self-pressurization crystallization kettle to carry out crystallization at 180° C. for 48 h;
[0068] (2) the crystallized sample of step (1) was filtered and washed with deionized water to neutral, then placed in an oven for drying at 150° C. for 2 h; the dried solid was placed in a muffle furnace, the temperature was raised from room temperature (25° C.) to 550° C. at a temperature rise rate of 2° C./min under a flowing air atmosphere, the dried solid was then roasted at a constant temperature of 550° C. for 12 h, and subsequently cooled naturally to room temperature to prepare the composite ZSM-5 molecular sieve M2. The composite ZSM-5 molecular sieve had a length of 40 μm, a height of 15 μm, a width of 14 μm, and a specific surface area of 340 m.sup.2/g.
[0069] The ratio of the number of sinusoidal pore openings to the number of straight pore openings on the external surface of the composite ZSM-5 molecular sieve, and the values of Y.sub.1 and Y.sub.2 of the composite ZSM-5 molecular sieve were shown in Table 1.
Example 3
[0070] (1) 62.4 g of ethyl orthosilicate was mixed with aluminum sulfate, aqueous solution of tetrapropylammonium hydroxide (25 wt %), ethylenediamine and water, wherein the used amounts of said raw materials satisfied SiO.sub.2:Al.sub.2O.sub.3:tetrapropylammonium hydroxide:ethylenediamine:water=100:0.8:4:36:2,000 (molar ratio), potassium hydroxide was added to adjust the pH to 13, then stirred uniformly for 30 min, the mixture was poured into a rotary self-pressurization crystallization kettle to carry out crystallization at 150° C. for 60 h;
[0071] (2) the crystallized sample of step (1) was filtered and washed with deionized water to neutral, then placed in an oven for drying at 150° C. for 2 h; the dried solid was placed in a muffle furnace, the temperature was raised from room temperature (25° C.) to 550° C. at a temperature rise rate of 5° C./min under a flowing air atmosphere, the dried solid was then roasted at a constant temperature of 550° C. for 12 h, and subsequently cooled naturally to room temperature to prepare the composite ZSM-5 molecular sieve M3. The composite ZSM-5 molecular sieve had a length of 33 μm, a height of 12 μm, a width of 15 μm, and a specific surface area of 300 m.sup.2/g.
[0072] The ratio of the number of sinusoidal pore openings to the number of straight pore openings on the external surface of the composite ZSM-5 molecular sieve, and the values of Y.sub.1 and Y.sub.2 of the composite ZSM-5 molecular sieve were shown in Table 1.
Example 4
[0073] (1) 18 g of solid silica gel powder (with a silica content more than 99 wt %) was mixed with sodium metaaluminate, tetrapropylammonium bromide, ethanolamine and water, wherein the used amounts of said raw materials satisfied SiO.sub.2:Al.sub.2O.sub.3:tetrapropylammonium bromide:ethanolamine:water=100:0.7:5:60:1,000 (molar ratio), sodium hydroxide was added to adjust the pH to 12.5, then stirred uniformly for 30 minutes, the mixture was poured into a rotary self-pressurization crystallization kettle to carry out crystallization at 170° C. for 24 h;
[0074] (2) the crystallized sample of step (1) was filtered and washed with deionized water to neutral, then placed in an oven for drying at 120° C. for 2 h; the dried solid was placed in a muffle furnace, the temperature was raised from room temperature (25° C.) to 550° C. at a temperature rise rate of 5° C./min under a flowing air atmosphere, the dried solid was then roasted at a constant temperature of 550° C. for 5 h, and subsequently cooled naturally to room temperature to prepare the composite ZSM-5 molecular sieve M4. The composite ZSM-5 molecular sieve had a length of 16 μm, a height of 5 μm, a width of 8 μm, and a specific surface area of 314 m.sup.2/g.
[0075] The ratio of the number of sinusoidal pore openings to the number of straight pore openings on the external surface of the composite ZSM-5 molecular sieve, and the values of Y.sub.1 and Y.sub.2 of the composite ZSM-5 molecular sieve were shown in Table 1.
Example 5
[0076] (1) 60 g of a silica sol solution (30 wt %) was mixed with sodium metaaluminate, aqueous solution of tetraethylammonium hydroxide (25 wt %), ethylamine and water, wherein the used amounts of said raw materials satisfied SiO.sub.2:Al.sub.2O.sub.3:tetraethylammonium hydroxide:ethylamine:water=100:0.8:3:45:4,000 (molar ratio), sodium hydroxide was added to adjust the pH to 11.6, then stirred uniformly for 30 minutes, the mixture was poured into a rotary self-pressurization crystallization kettle to carry out crystallization at 170° C. for 24 h;
[0077] (2) the crystallized sample of step (1) was filtered and washed with deionized water to neutral, then placed in an oven for drying at 120° C. for 2 h; the dried solid was placed in a muffle furnace, the temperature was raised from room temperature (25° C.) to 550° C. at a temperature rise rate of 5° C./min under a flowing air atmosphere, the dried solid was then roasted at a constant temperature of 550° C. for 5 h, and subsequently cooled naturally to room temperature to prepare the composite ZSM-5 molecular sieve M5. The composite ZSM-5 molecular sieve had a length of 27 μm, a height of 14 μm, a width of 10 μm, and a specific surface area of 354 m.sup.2/g.
[0078] The ratio of the number of sinusoidal pore openings to the number of straight pore openings on the external surface of the composite ZSM-5 molecular sieve, and the values of Y.sub.1 and Y.sub.2 of the composite ZSM-5 molecular sieve were shown in Table 1.
Example 6
[0079] (1) 18 g of solid silica gel powder (with a silica content more than 99 wt %) was mixed with sodium metaaluminate, aqueous solution of tetrabutylammonium hydroxide (25 wt %), ethylamine and water, wherein the used amounts of said raw materials satisfied SiO.sub.2:Al.sub.2O.sub.3:tetrabutylammonium hydroxide:ethanol:water=100:0.6:2:40:3,000 (molar ratio), sodium hydroxide was added to adjust the pH to 13, then stirred uniformly for 30 minutes, the mixture was poured into a rotary self-pressurization crystallization kettle to carry out crystallization at 170° C. for 24 h;
[0080] (2) the crystallized sample of step (1) was filtered and washed with deionized water to neutral, then placed in an oven for drying at 120° C. for 2 h; the dried solid was placed in a muffle furnace, the temperature was raised from room temperature (25° C.) to 550° C. at a temperature rise rate of 5° C./min under a flowing air atmosphere, the dried solid was then roasted at a constant temperature of 550° C. for 5 h, and subsequently cooled naturally to room temperature to prepare the composite ZSM-5 molecular sieve M6. The composite ZSM-5 molecular sieve had a length of 10 μm, a height of 4 μm, a width of 4 μm, and a specific surface area of 370 m.sup.2/g.
[0081] The ratio of the number of sinusoidal pore openings to the number of straight pore openings on the external surface of the composite ZSM-5 molecular sieve, and the values of Y.sub.1 and Y.sub.2 of the composite ZSM-5 molecular sieve were shown in Table 1.
Example 7
[0082] The molecular sieve was prepared according to the method of Example 1, except that the used amounts of said raw materials satisfied SiO.sub.2:Al.sub.2O.sub.3:tetrapropylammonium bromide:n-butylamine:water=100:0.67:2:60:3,333 (molar ratio), so as to prepare a composite ZSM-5 molecular sieve M7. The composite ZSM-5 molecular sieve had a length of 30 μm, a height of 13 μm, a width of 13 μm, and a specific surface area of 300 m.sup.2/g.
[0083] The ratio of the number of sinusoidal pore openings to the number of straight pore openings on the external surface of the composite ZSM-5 molecular sieve, and the values of Y.sub.1 and Y.sub.2 of the composite ZSM-5 molecular sieve were shown in Table 1.
Example 8
[0084] The molecular sieve was prepared according to the method of Example 1, except that the used amounts of said raw materials satisfied SiO.sub.2:Al.sub.2O.sub.3:tetrapropylammonium bromide:n-butylamine:water=100:0.67:2:6:3,333 (molar ratio), so as to prepare a composite ZSM-5 molecular sieve M8. The composite ZSM-5 molecular sieve had a length of 10 μm, a height of 2 μm, a width of 3 μm, and a specific surface area of 410 m.sup.2/g.
[0085] The ratio of the number of sinusoidal pore openings to the number of straight pore openings on the external surface of the composite ZSM-5 molecular sieve, and the values of Y.sub.1 and Y.sub.2 of the composite ZSM-5 molecular sieve were shown in Table 1.
Example 9
[0086] The molecular sieve was prepared according to the method of Example 2, except that the pH was adjusted to 11 to prepare a composite ZSM-5 molecular sieve M9. The composite ZSM-5 molecular sieve had a length of 40 μm, a height of 20 μm, a width of 15 μm, and a specific surface area of 320 m.sup.2/g.
[0087] The ratio of the number of sinusoidal pore openings to the number of straight pore openings on the external surface of the composite ZSM-5 molecular sieve, and the values of Y.sub.1 and Y.sub.2 of the composite ZSM-5 molecular sieve were shown in Table 1.
Example 10
[0088] The molecular sieve was prepared according to the method of Example 1, except that the used amounts of said raw materials satisfied SiO.sub.2:Al.sub.2O.sub.3:tetrapropylammonium bromide:n-butylamine:water=100:0.67:4.5:35.3:300 (molar ratio), so as to prepare a composite ZSM-5 molecular sieve M10. The composite ZSM-5 molecular sieve had a length of 15 μm, a height of 4 μm, a width of 4 μm, and a specific surface area of 440 m.sup.2/g.
[0089] The ratio of the number of sinusoidal pore openings to the number of straight pore openings on the external surface of the composite ZSM-5 molecular sieve, and the values of Y.sub.1 and Y.sub.2 of the composite ZSM-5 molecular sieve were shown in Table 1.
Comparative Example 1
[0090] The molecular sieve was prepared according to the method of Example 1, except that the used amounts of said raw materials satisfied SiO.sub.2:Al.sub.2O.sub.3:tetrapropylammonium bromide:n-butylamine:water=100:0.67:1.5:60:3,333 (molar ratio), so as to prepare a composite ZSM-5 molecular sieve D1.
[0091] The SEM spectrogram of the composite ZSM-5 molecular sieve D1 was shown in
Comparative Example 2
[0092] The molecular sieve was prepared according to the method of Example 1, except that the used amounts of said raw materials satisfied SiO.sub.2:Al.sub.2O.sub.3:tetrapropylammonium bromide:n-butylamine:water=100:0.67:6:2:3,333 (molar ratio), so as to prepare a composite ZSM-5 molecular sieve D2.
[0093] The SEM spectrogram of the composite ZSM-5 molecular sieve D2 was shown in
Comparative Example 3
[0094] The molecular sieve was prepared according to the method of Example 1, except that n-butylamine was replaced with an equivalent molar weight of tetrabutylammonium hydroxide to prepare the ZSM-5 molecular sieve D3.
[0095] The ratio of the number of sinusoidal pore openings to the number of straight pore openings on the external surface of the ZSM-5 molecular sieve, and the values of Y.sub.1 and Y.sub.2 of the composite ZSM-5 molecular sieve were shown in Table 1.
Comparative Example 4
[0096] The molecular sieve was prepared according to the method of Example 1, except that tetrapropylammonium bromide was replaced with an equivalent molar weight of ethanol amine to prepare the ZSM-5 molecular sieve D4.
[0097] The ratio of the number of sinusoidal pore openings to the number of straight pore openings on the external surface of the ZSM-5 molecular sieve, and the values of Y.sub.1 and Y.sub.2 of the composite ZSM-5 molecular sieve were shown in Table 1.
Comparative Example 5
[0098] The molecular sieve was prepared according to the method of Example 1, except that n-butylamine was replaced with an equivalent molar weight of triethylamine to prepare the ZSM-5 molecular sieve D5.
[0099] The ratio of the number of sinusoidal pore openings to the number of straight pore openings on the external surface of the ZSM-5 molecular sieve, and the values of Y.sub.1 and Y.sub.2 of the composite ZSM-5 molecular sieve were shown in Table 1.
Comparative Example 6
[0100] The molecular sieve was prepared according to the method of Example 1, except that n-butylamine was replaced with an equivalent molar weight of triethanolamine to prepare the ZSM-5 molecular sieve D6.
[0101] The ratio of the number of sinusoidal pore openings to the number of straight pore openings on the external surface of the ZSM-5 molecular sieve, and the values of Y.sub.1 and Y.sub.2 of the composite ZSM-5 molecular sieve were shown in Table 1.
Comparative Example 7
[0102] The molecular sieve was prepared according to the method of Example 2, except that the pH was adjusted to 13.8 to prepare the ZSM-5 molecular sieve D7.
[0103] The ratio of the number of sinusoidal pore openings to the number of straight pore openings on the external surface of the ZSM-5 molecular sieve, and the values of Y.sub.1 and Y.sub.2 of the composite ZSM-5 molecular sieve were shown in Table 1.
Example 11
[0104] The composite ZSM-5 molecular sieves M1-M10 and ZSM-5 molecular sieves D1-D7 prepared in the above Examples and Comparative Examples were used in the alkylation reaction of toluene methanol under the following reaction conditions: a reaction temperature of 470° C., a reaction pressure of atmospheric pressure, the reaction was carried out under a hydrogen atmosphere, a molar ratio of toluene to methanol in the liquid feedstock was 6:1, the feedstock was fed by a peristaltic pump, the feeding rate was 0.03 mL/min, and the used amount of said molecular sieve catalyst was 0.2 g.
[0105] The toluene conversion and p-xylene selectivity were calculated after the reaction was completed, the results were shown in Table 1.
Toluene conversion=(molar amount of toluene feed−molar amount of toluene discharge)/molar amount of toluene feed×100%;
P-xylene selectivity=molar amount of p-xylene discharge/(molar amount of p-xylene discharge+molar amount of m-xylene discharge+molar amount of o-xylene discharge)×100%.
TABLE-US-00001 TABLE 1 The ratio of the number P- of sinusoidal pore Toluene xylene openings to the number conver- selectiv- of straight pore openings Y.sub.1 Y.sub.2 sion % ity % Example 1 2.9 1000 150 10.4 99.4 Example 2 2.6 980 150 10.5 98.6 Example 3 1.7 930 140 11.0 97.3 Example 4 1.4 930 130 10.3 97.1 Example 5 1.3 870 125 7.8 95.1 Example 6 1.2 710 120 8.3 90.3 Example 7 1.5 610 140 9.2 82.2 Example 8 1.0 530 154 8.0 84.4 Example 9 1.8 500 136 10.1 87.5 Example 10 0.9 630 135 9.1 81.4 Comparative 0.8 150 147 11.1 79.5 Example 1 Comparative 0.6 130 134 11.4 73.6 Example 2 Comparative 0.8 125 125 12.7 78.2 Example 3 Comparative 0.7 148 150 12.9 60.3 Example 4 Comparative 0.4 120 145 15 34.0 Example 5 Comparative 0.4 130 150 16 24 Example 6 Comparative 0.4 138 150 16 24 Example 7
[0106] As can be seen from the above Examples, Comparative Examples and results show in Table 1, a single crystal of the composite ZSM-5 molecular sieve comprises a main crystal and a twin crystal; wherein the main crystal and the twin crystal are both ZSM-5 crystals; a crystal plane [010] of the main crystal is covered by a crystal plane [100] of the twin crystal, such that the ratio of the number of sinusoidal pore openings to the number of straight pore openings on the external surface of the single crystal of the composite ZSM-5 molecular sieve is high, such as large than 0.8; in addition, as shown in data of the molar ratio Y.sub.1 of Si element to Al element within 10 nm of the surface of the composite ZSM-5 molecular sieve and the molar ratio Y.sub.2 of Si element to Al element of the composite ZSM-5 molecular sieve as a whole, the composite ZSM-5 molecular sieve of the present disclosure is aluminum-poor on the surface and aluminum-rich on the inside; as compared with the result data of the Comparative Examples 1-7, the composite ZSM-5 molecular sieve of the present disclosure is applied in the alkylation reaction of toluene methanol to prepare p-xylene, it can effectively improve the p-xylene selectivity in the alkylation reaction of toluene methanol to prepare p-xylene.
[0107] The above content describes in detail the preferred embodiments of the present disclosure, but the present disclosure is not limited thereto. A variety of simple modifications can be made in regard to the technical solutions of the present disclosure within the scope of the technical concept of the present disclosure, including a combination of individual technical features in any other suitable manner, such simple modifications and combinations thereof shall also be regarded as the content disclosed by the present disclosure, each of them falls into the protection scope of the present disclosure.