阅读说明：本技术 一种应用于低碳烷烃芳构化的纳米BaKL沸石合成方法 (Synthesis method of nano BaKL zeolite applied to aromatization of low-carbon alkane ) 是由 张文赟 于 2021-09-01 设计创作，主要内容包括：一种应用于低碳烷烃芳构化的纳米BaKL沸石合成方法,其属于沸石制备技术领域。该方法将钡源、碱源、铝源、硅源和水按摩尔比混合制得溶胶,在固态或动态晶化下,得到纳米尺度的BaKL沸石。本发明可在低硅铝比投料、不加模板剂和结构导向剂的条件下,合成出具有纳米尺度、高结晶度和多级孔结构的BaKL沸石。将本发明所提供的BaKL沸石用于低碳烷烃芳构化反应中,可以明显提高芳烃收率特别是C8芳烃收率。与传统方法相比,该方法制备工艺简单,原料利用率高,成本低,具有广阔的应用前景。(A synthesis method of nanometer BaKL zeolite applied to aromatization of low-carbon alkane belongs to the technical field of zeolite preparation. The method mixes barium source, alkali source, aluminum source, silicon source and water according to the molar ratio to prepare sol, and obtains the nano-scale BaKL zeolite under the condition of solid state or dynamic crystallization. The invention can synthesize the BaKL zeolite with nano-scale, high crystallinity and hierarchical pore structure under the conditions of feeding with low silicon-aluminum ratio and without adding a template agent and a structure directing agent. When the BaKL zeolite provided by the invention is used in the aromatization reaction of low-carbon alkane, the yield of aromatic hydrocarbon, particularly the yield of C8 aromatic hydrocarbon, can be obviously improved. Compared with the traditional method, the method has the advantages of simple preparation process, high utilization rate of raw materials, low cost and wide application prospect.)

1. A nanometer BaKL zeolite applied to aromatization of low-carbon alkane is characterized in that: the BaKL zeolite has an LTL structure, and the mole ratio of a barium source, a potassium source, an aluminum source and a silicon source in the zeolite is BaO: K₂O:Al₂O₃:SiO₂ =0.0005~8 : 0.1~9 : 1 : 1~20。

2. The synthesis method of nanometer BaKL zeolite applied to aromatization of lower alkanes according to claim 1 is characterized in that: comprises the following steps of (a) carrying out,

(1) barium source, potassium source, aluminum source, silicon source and water are mixed according to BaO: K₂O:Al₂O3:SiO₂:H₂Mixing O = 0.0005-8: 0.1-9: 1: 1-20: 50-500 molar ratio to prepare sol;

(2) stirring and aging the sol prepared in the step (1);

(3) and (3) placing the sol prepared in the step (2) in a closed container, and crystallizing at 100-260 ℃ for 12 h-10 d to obtain the nano BaKL zeolite.

3. The synthesis method of nanometer BaKL zeolite applied to aromatization of lower alkanes according to claim 2, which is characterized in that: the molar ratio of the barium source, the potassium source, the aluminum source, the silicon source and the water is BaO to K₂O:Al₂O₃:SiO₂:H₂O=0.001~1 : 0.5~5 : 1 : 3~16 : 70~400。

4. The synthesis method of nanometer BaKL zeolite applied to aromatization of lower alkanes according to claim 2, which is characterized in that: the volume of the closed container is 30 mL-1 m³。

5. The synthesis method of nanometer BaKL zeolite applied to aromatization of lower alkanes according to claim 2, which is characterized in that: the crystallization process is dynamic crystallization or static crystallization.

6. The synthesis method of nanometer BaKL zeolite applied to aromatization of lower alkanes according to claim 2, which is characterized in that: the crystallization temperature in the crystallization process is 110-185 ℃, and the crystallization time is 6-36 h.

7. The synthesis method of nanometer BaKL zeolite applied to aromatization of lower alkanes according to claim 2, which is characterized in that: the aging temperature is room temperature, and the aging time is 4-24 h.

8. The synthesis method of nanometer BaKL zeolite applied to aromatization of lower alkanes according to claim 2, which is characterized in that: the barium source is one or more than two of barium nitrate, barium chloride, barium hydroxide and barium acetate; the potassium source is one or more of potassium hydroxide, potassium chloride and potassium oxide; the aluminum source is one or more than two of pseudo-boehmite, activated alumina, aluminum hydroxide, aluminum isopropoxide, hydrated alumina, potassium aluminate, aluminum trichloride, aluminum sulfate and aluminum nitrate; the silicon source is one or more than two of silica sol, ethyl orthosilicate, white carbon black and water glass.

9. Use of nano-BaKL zeolite prepared according to the process of claims 2 to 8, characterised in that: the nanometer BaKL zeolite is used as a catalyst carrier, and a metal BaKL zeolite catalyst is prepared after metal is loaded, wherein the metal is one or more than two of Pt, Ru, Pd and Sn; the loading amount of the metal is 0.05-4.0% of the mass of the carrier.

10. Use of a metallic BaKL zeolite catalyst according to claim 9, characterised in that: the metal BaKL zeolite catalyst is used for aromatization reaction of low-carbon alkane, and the number of carbon atoms in the low-carbon alkane is 6-8;

the reaction conditions of the aromatization are as follows: the mass space velocity of the alkane is 0.8-4 h^-1The molar ratio of hydrogen to alkane is 0.2-6.0: 1, the reaction pressure is 0.1-3 MPa, and the reaction temperature is 250-550 ℃.

Technical Field

The invention relates to a synthesis method of nano-scale BaKL zeolite applied to aromatization of low-carbon alkane.

Background

Aromatic hydrocarbon occupies a pivotal position in chemical industry, is an important bulk chemical and basic chemical raw material, is widely used for manufacturing various important production and living materials, is also an important blending component of high-quality gasoline, and is related to the national civilization. China is the largest world consuming country of benzene and paraxylene, and the demand is still rising day by day with the development of socioeconomic. In 2018, the external dependence of the aromatic hydrocarbon in China is as high as 20-60%. The development of the related industrial application technology of the aromatization of the low-carbon alkane has important significance for reducing the external dependence of the aromatic hydrocarbon in China.

The Pt/KL catalyst is a base-catalyzed aromatization catalyst with excellent aromatization performance, and has the advantages of high liquid yield and high aromatic yield compared with acid-catalyzed aromatization. However, the low selectivity of the catalyst to aromatics and the short single-pass life are the main defects, and the industrial application of the catalyst is limited. In order to improve the stability of the catalyst, a series of modifications have been made to the L zeolite.

The Pt/KL catalyst is a base-catalyzed aromatization catalyst with excellent aromatization performance, and has the advantages of high liquid yield and high aromatic yield compared with acid-catalyzed aromatization. But the catalyst has the main disadvantages of low aromatic selectivity and low single pass life. The above problems can be effectively solved by loading the second metal or pore-expanding the KL zeolite. For this reason, a series of improvements have been made in the synthesis of zeolite L.

For example, the results disclosed in chinese patent application No. CN 201310137862 show that the structure and properties of the prepared FeKL heteroatom zeolite are changed by introducing the heteroatom Fe, and the catalyst loaded with Pt has relatively good n-hexane aromatization performance.

Chinese patent application publication No. CN101746774A discloses a method for synthesizing L zeolite containing Sn heteroatom, and the catalyst prepared by using the zeolite to load Pt not only has higher benzene selectivity but also better stability when used in n-hexane aromatization reaction.

However, the above method still has the problem of carbon deposition and the like, which adversely affects the arylation.

Ba element is the most popular second metal in current research, because the strong electron-donating ability of Ba element enriches Pt electrons, and improves the aromatization performance of the catalyst while inhibiting hydrogenolysis so as to increase the selectivity of aromatic hydrocarbon; and the pore expansion of KL zeolite can promote Pt²⁺Enters the main pore canal of the zeolite, and can improve the carbon capacity of the catalyst, thereby improving the one-way service life of the catalyst.

For example, US4434311 and US4435283 both disclose a preparation method of a Pt/KL aromatization catalyst, which comprises the steps of co-exchanging Ba salt with a Pt precursor solution, and then drying and roasting to obtain a catalyst, wherein the catalyst can improve the selectivity of aromatic hydrocarbon, but the improvement range is limited; meanwhile, Ba competes with Pt for exchange, which may cause a problem of reduction of Pt exchange degree, thereby affecting catalyst activity.

In the process of synthesizing KL zeolite, how to improve the yield of KL zeolite is always a concern, and researchers have done a lot of work.

Chinese patent publication No. CN85103013B discloses that the Si/Al ratio in the feed of the synthesis system is increased, and the feed ratio (molar ratio) is 6.6K₂O:Al₂O₃:28SiO₂:440H₂And O, crystallizing the KL zeolite for 60-72 hours at 100 ℃ in a pressure kettle. The main problems of the method are that the ratio of the fed silicon to the aluminum is higher, the utilization rate of silicon is low and the synthesis cost is high.

Disclosure of Invention

The invention aims to overcome the defects of the prior art, improve the yield of KL zeolite and reduce the synthesis cost; the diffusion path of molecules is shortened, so that the aromatic selectivity of the catalyst is improved, and the one-way service life of the catalyst is prolonged; successfully performs pilot test on the synthesis process, leads the synthesis process to be closer to industrialization, and provides a method for synthesizing nano BaKL zeolite

The scheme for solving the technical problems is as follows:

a nanometer BaKL zeolite used for aromatization of low-carbon alkane has an LTL structure confirmed by the International Zeolite Association, and the synthesis method is characterized in that: mixing a barium source, a potassium source, an aluminum source, a silicon source and water to prepare sol, aging and crystallizing to obtain the nano BaKL zeolite, comprising the following steps,

(1) barium source, potassium source, aluminum source, silicon source and water are mixed according to BaO: K₂O:Al₂O₃:SiO₂:H₂O =0.0005 to 8: 0.1 to 9: 1: 1 to 20: 50 to 500 by mol ratio to prepare a sol,

(2) stirring and aging the sol prepared in the step (1),

(3) and (3) placing the sol prepared in the step (2) in a closed container, and crystallizing at 100-260 ℃ for 12 h-10 d to obtain the nano BaKL zeolite.

The molar ratio of the barium source, the potassium source, the aluminum source, the silicon source and the water is preferably BaO to K₂O:Al₂O₃:SiO₂:H₂O = 0.001-1: 0.5-5: 1: 3-16: 70-400. The silicon-aluminum ratio of the fed materials is low, the crystallization of the product is good, and the yield can reach 91 percent at most.

The volume of the closed container is 30 mL-1 m³From pilot to pilot.

The crystallization process of the invention is dynamic crystallization or static crystallization. Generally, industrially produced zeolites are dynamically crystallized. The dynamic crystallization of the invention simulates the industrial production condition and is between 10L and 1m³And (4) successfully crystallizing in a closed kettle to obtain the LTL zeolite containing Ba.

The crystallization temperature in the crystallization process is 110-185 ℃, and the crystallization time is 6-36 h.

The aging temperature is room temperature, and the time is 4-24 hours.

The barium source is one or more than two of barium nitrate, barium chloride, barium hydroxide and barium acetate; the potassium source is one or more of potassium hydroxide, potassium chloride and potassium oxide; the aluminum source is one or more than two of pseudo-boehmite, activated alumina, aluminum hydroxide, aluminum isopropoxide, hydrated alumina, potassium aluminate, aluminum trichloride, aluminum sulfate and aluminum nitrate; the silicon source is one or more than two of silica sol, ethyl orthosilicate, white carbon black and water glass.

The nanometer BaKL zeolite is used as a carrier to prepare the catalyst for aromatization of the low-carbon alkane.

The catalyst specifically comprises metal loaded on the carrier, wherein the metal is one or more of Pt, Ru, Pd and Sn, and the loading amount of the metal is 0.05-4.0%.

The aromatization of the normal alkane can be carried out in a fixed bed reactor, and the number of carbon atoms in the normal alkane is 6, 7 or 8.

The reaction conditions of the aromatization may specifically be: the mass space velocity of the n-alkane is 0.8-4 h^-1The molar ratio of the hydrogen to the n-alkane is 0.2-6.0: 1, the reaction pressure is 0.1-3 MPa, and the reaction temperature is 250-550 ℃.

In conclusion, the synthesis method of the nanometer BaKL zeolite applied to aromatization of the low-carbon alkane has the following advantages:

ba element is the most popular second metal in current research, because the strong electron-donating ability of Ba element enriches Pt electrons, and improves the aromatization performance of the catalyst while inhibiting hydrogenolysis so as to increase the selectivity of aromatic hydrocarbon; and the pore expansion of KL zeolite can promote Pt²⁺Enters the main pore canal of the zeolite, and can improve the carbon capacity of the catalyst, thereby improving the one-way service life of the catalyst. Under the conditions of low silicon-aluminum ratio feeding and no addition of a template agent and a structure directing agent, the BaKL zeolite with the nano-scale, high crystallinity and a hierarchical pore structure is synthesized. When the BaKL zeolite provided by the invention is used in the aromatization reaction of low-carbon alkane, the yield of aromatic hydrocarbon, particularly the yield of C8 aromatic hydrocarbon, can be obviously improved. Compared with the traditional method, the method has the advantages of simple preparation process, high raw material utilization rate, high yield up to 91 percent, low cost and wide application prospect.

Drawings

FIG. 1 is an XRD spectrum of a sample of example 1 of the present invention.

FIG. 2 is a graph showing the distribution of the wells of the sample in example 1 of the present invention.

FIG. 3 is an SEM photograph of a sample in example 1 of the present invention.

Detailed Description

The following examples further illustrate the invention but are not intended to limit the invention thereto.

TABLE 1 Synthesis conditions of examples 1 to 5 of the present invention

Examples

K2O:SiO2:Al2O3:BaO:H2O

Ba source

Time of crystallization

Crystallization temperature

Mode of crystallization

Scale of

1

2.0 : 7.1 : 1.0 : 0.008 : 190

Barium nitrate

18 h

170 °C

Dynamic state

200 mL

2

0.5 : 8.5 : 1.0 : 0.001 : 70

Barium chloride

6 h

185 °C

Static state

30 mL

3

5.0 : 16 : 1.0 : 1.0 : 400

Barium acetate

24 h

110°C

Dynamic state

2 L

4

3.0 : 3.0 : 1.0 : 0.01 : 250

Barium hydroxide

36 h

175°C

Dynamic state

10 L

5

2.5 : 8.0 : 1.0 : 0.03 : 210

Barium nitrate

22 h

175°C

Dynamic state

1 m3

Example 1

12.25 g KOH was weighed in a 500 mL beaker, 10 g pure water was added, and after stirring well, 7.06 g Al (OH) was added₃And heating to 95 ℃ and stirring to clarify the solution. After the solution was cooled, 117.12 g of pure water was added, 0.097g of barium nitrate was added, and stirring was continued. 49.48 g of silica sol was weighed into another 500 mL beaker, and the clear Al (OH) was added via a separatory funnel₃The solution was added dropwise to the silica sol and stirring was continued for 8 h. StopStirring, and placing the gel in a 200 mL crystallization kettle. And (4) placing the crystallization kettle into an oven, and dynamically crystallizing at 170 ℃ for 18 h. After crystallization is finished, the crystallization kettle is taken out, and then the sample is centrifugally washed by pure water until the pH value is 7 or 8. The sample was transferred to a crucible and placed in a 120 ℃ oven for drying for 12 h, with a yield of 91%.

Grinding the molecular sieve into powder, and analyzing by XRD spectrogram, the molecular sieve is BaKL and contains mesopores as shown in figures 1 and 2. The resulting molecular sieve was cylindrical, as shown in FIG. 3.

The catalyst was prepared by using the above-mentioned BaKL zeolite supported metal Pt (0.5 wt%), and the aromatization performance thereof was evaluated in a fixed bed reactor using n-octane as a raw material. The mass space velocity (WHSV) is 1h^-1The hydrogen-hydrocarbon ratio was 6 (molar ratio), the reaction pressure was 1MPa, and the reaction temperature was 500 ℃. Wherein the liquid phase product is analyzed off line after being condensed, and the gas phase product is analyzed on line.

The catalyst prepared by the carrier shows excellent catalytic performance in the aromatization reaction of n-octane, and under the condition of 96 percent of conversion rate, the aromatic hydrocarbon yield reaches 60 percent, the C8 aromatic hydrocarbon yield reaches 26 percent, the toluene yield reaches 17 percent, the benzene yield reaches 14 percent, and the liquid yield reaches 82 percent. From the data, the catalyst prepared by the nanometer BaKL zeolite sieve has higher aromatic hydrocarbon yield and liquid yield in the aromatization reaction of n-octane,

example 2

1.53 g KOH was weighed in a 100 mL beaker, 2g pure water was added, and after stirring well, 3.53 g Al (OH) was added₃And heating to 95 ℃ and stirring to clarify the solution. After the solution was cooled, 9 g of pure water was added, 0.0061g of barium chloride was added, and stirring was continued. 30 g of silica sol was weighed into another 100 mL beaker, and the clear Al (OH) was added via a separatory funnel₃The solution was added dropwise to the silica sol and stirring was continued for 24 h. Stopping stirring, and filling the gel into a 30 mL crystallization kettle. And (4) putting the crystallization kettle into an oven, and statically crystallizing at 185 ℃ for 6 h. After crystallization is finished, the crystallization kettle is taken out, and then the sample is centrifugally washed by pure water until the pH value is 7 or 8. The sample was transferred to a crucible and placed in a 120 ℃ oven for drying for 12 h, with a yield of 67%. The molecular sieve is BaKL by XRD spectrogram analysis.

Example 3

130.13 g of KOH were weighed in a 2000 mL beaker, 100 g of pure water was added, and after stirring well, 30 g of Al (OH) was added₃And heating to 95 ℃ and stirring to clarify the solution. After the solution was cooled, 1030 g of pure water was added, 51.52g of barium acetate was added, and stirring was continued. 473.79 g of silica sol was weighed into a 2000 mL beaker, and the clear Al (OH) was added via a separatory funnel₃The solution was added dropwise to the silica sol and stirring was continued for 4 h. Stopping stirring, and filling the gel into a 2L crystallization kettle. And (3) putting the crystallization kettle into an oven, and dynamically crystallizing for 24 hours at the temperature of 110 ℃. After crystallization is finished, the crystallization kettle is taken out, and then the sample is centrifugally washed by pure water until the pH value is 7 or 8. The sample was transferred to a crucible and placed in a 120 ℃ oven for drying for 12 h, with a yield of 59%. The molecular sieve is BaKL by XRD spectrogram analysis.

Example 4

781 g KOH was weighed in a 10L bucket, 800 g pure water was added, and after stirring well, 300 g Al (OH) was added₃And heating to 95 ℃ and stirring to clarify the solution. After the solution was cooled, 7454.3 g of pure water was added, 5.152g of barium hydroxide was added, and stirring was continued. 473.79 g of silica sol was weighed into another 10L bucket, and then clarified Al (OH)₃The solution was added dropwise to the silica sol and stirring was continued for 10 h. Stopping stirring, and filling the gel into a 10L crystallization kettle. And (4) putting the crystallization kettle into an oven, and dynamically crystallizing at 175 ℃ for 36 h. After crystallization is finished, the crystallization kettle is taken out, and then the sample is centrifugally washed by pure water until the pH value is 7 or 8. The sample is transferred to a crucible and put into a 120 ℃ oven for drying for 12 h, and the yield is 85%. The molecular sieve is BaKL by XRD spectrogram analysis.

Example 5

672.35kg KOH was weighed, 152kg pure water was added, and 310kg Al (OH) was added after stirring well₃And heating to 95 ℃ and stirring to clarify the solution. After the solution was cooled, 6000.33kg of pure water was added, 15.97kg of barium nitrate was added, and stirring was continued. 2447.91 kg of silica sol were weighed out and the clear Al (OH)₃The solution was added dropwise to the silica sol and stirring was continued for 17 h. Stopping stirring, and filling the gel at 1m³In a crystallization kettle. And (4) putting the crystallization kettle into an oven, and dynamically crystallizing for 22 h at 175 ℃. After crystallization is finished, the crystallization kettle is taken out, and then the sample is centrifugally washed by pure water until the pH value is 7 or 8. Will be provided withThe sample was transferred to a crucible and placed in a 120 ℃ oven for drying for 12 h, with a yield of 73%. The molecular sieve is BaKL by XRD spectrogram analysis.