A kind of supported heteropolyacid catalyst and preparation method thereof

A heteropolyacid and catalyst technology, applied in the field of supported heteropolyacid catalyst and its preparation, can solve the problems of high equipment requirements, poor low-temperature activity, low initial temperature, etc., and achieve high low-temperature reaction activity and specific surface area The effect of increasing the concentration of reactants

Active Publication Date: 2022-07-12
CHINA PETROLEUM & CHEM CORP +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] At present, the catalyst used for methanol dehydration is generally Al 2 o 3 Or molecular sieves, wherein commonly used molecular sieves include aluminum phosphate, HZSM-5, HY, SAPO, etc., and they all have their own advantages and disadvantages: although alumina has high stability, the reaction temperature is high, and the requirements for reaction equipment are very high, resulting in The cost is high; molecular sieve catalysts have strong acidity and low initial temperature, but they also have the disadvantages of many by-products, easy carbon deposition, and easy deactivation
When the above-mentioned catalyst is used to process pure methanol raw materials under normal pressure, its selectivity is relatively high, but its low-temperature activity is not good, and further improvement is needed.

Method used

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  • A kind of supported heteropolyacid catalyst and preparation method thereof
  • A kind of supported heteropolyacid catalyst and preparation method thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0041] (1) Catalyst preparation

[0042] Weigh 600g of ammonium phosphate and dissolve it in 2000mL of deionized water to obtain solution A; grind 1000g of petroleum coke to powder, then add it to solution A, leave it for 1.5h, and then filter, the obtained solid sample is placed in an oven at 110°C Dry for 5h. The above-mentioned dried solid samples were pretreated with water vapor at 200 °C for 3 h (the volumetric space velocity of the water vapor gas was 1200 h). -1 ), then the temperature was raised to 400 °C, continued to be pretreated for 3 h, and then cooled to 60 °C under nitrogen protection to obtain pretreated petroleum coke.

[0043] 1000g of the above-obtained pretreated petroleum coke, 38.5g of lanthanum nitrate and 2000g of potassium hydroxide were mixed uniformly, placed in a microwave oven with a microwave frequency of 2450MHz, evacuated, and heated to 500 under the condition that the microwave power was 0.3kw. ℃, kept constant for 40min, then passed nitrogen...

Embodiment 2

[0049] (1) Catalyst preparation

[0050] Weigh 500 g of diammonium hydrogen phosphate, dissolve it in 2000 mL of deionized water to obtain solution A; grind 1000 g of petroleum coke to powder, then add it to solution A, leave it for 1.5 hours, and then filter, and the obtained solid sample is placed in an oven at 110 Dry at ℃ for 5h. The dried solid samples were pretreated with water vapor for 3h at 200°C (the volumetric space velocity of water vapor was 1000h). -1 ), then the temperature was raised to 400 °C, continued to be pretreated for 3 h, and then cooled to 60 °C under nitrogen protection to obtain pretreated petroleum coke.

[0051] 1000g of the above-obtained pretreated petroleum coke, 62.2g of lanthanum nitrate and 3000g of potassium hydroxide were mixed uniformly, placed in a microwave oven with a microwave frequency of 2450MHz, evacuated, and heated to 600 under the condition that the microwave power was 0.3kw. ℃, kept constant for 20min, then passed nitrogen to ...

Embodiment 3

[0057] (1) Catalyst preparation

[0058] Weigh 400 g of ammonium dihydrogen phosphate and dissolve it in 2000 mL of deionized water to obtain solution A; grind 1000 g of petroleum coke to powder, then add it to solution A, leave it for 1.5 hours, and then filter, and the obtained solid sample is placed in an oven at 110 Dry at ℃ for 5h. The dried solid samples were pretreated with water vapor for 3h at 200°C (the volumetric space velocity of water vapor was 800h). -1 ), then the temperature was raised to 400 °C, continued to be pretreated for 3 h, and then cooled to 60 °C under nitrogen protection to obtain pretreated petroleum coke.

[0059] 1000g of the above-obtained pretreated petroleum coke, 89.9g of lanthanum nitrate and 4000g of potassium hydroxide were mixed uniformly, placed in a microwave oven with a microwave frequency of 2450MHz, evacuated, and heated to 400 under the condition that the microwave power was 0.3kw. ℃, kept constant for 60min, then passed nitrogen t...

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Abstract

The invention discloses a supported heteropolyacid catalyst and a preparation method thereof. The catalyst comprises an active component, an auxiliary agent and a carrier; the active component is a heteropolyacid, and the auxiliary agent is selected from one of rare earth elements Or several, the carrier is petroleum coke-based activated carbon. The preparation method is as follows: mixing petroleum coke, a metal soluble salt containing an auxiliary agent and an activator, mixing uniformly and then activating, and then performing washing and drying treatments; finally, introducing a heteropolyacid, and then drying and roasting to obtain a supported heteropolyacid catalyst. The catalyst prepared by the method of the invention has high low-temperature activity, selectivity and anti-coking performance.

Description

technical field [0001] The invention belongs to the field of chemical industry, and relates to a catalytic material and a preparation method thereof, in particular to a supported heteropolyacid catalyst and a preparation method thereof. Background technique [0002] Dimethy Ether (abbreviated DME) is a colorless, non-toxic gas at normal temperature and pressure, which can be compressed into a liquid. DME is an important organic chemical raw material and chemical intermediate, which can be used in aerosols, refrigerants, alkylating agents, pharmaceuticals, cosmetics, fuels and other industries. [0003] Dimethyl ether was first obtained by rectifying the by-product of high-pressure methanol production, and soon developed into two processes: methanol dehydration and synthesis gas direct synthesis. The liquid phase method of methanol dehydration to produce dimethyl ether, the reaction is carried out in the liquid phase, the main disadvantage is that the equipment is seriously ...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): B01J27/188B01J31/26B01J31/16B01J35/10C07C41/09C07C43/04
CPCB01J27/188B01J23/30B01J35/1023B01J35/1028B01J35/1042B01J35/1047C07C41/09B01J2523/00C07C43/043B01J2523/3712B01J2523/41B01J2523/69Y02P20/52
Inventor 金浩刘璐朱慧红杨光孙素华杨涛
Owner CHINA PETROLEUM & CHEM CORP
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