A kind of vanadyl phosphate catalyst, its preparation method and application

A technology of vanadyl phosphate catalyst and vanadium source, which is applied in the direction of catalyst activation/preparation, chemical instruments and methods, physical/chemical process catalysts, etc. It can solve problems such as low conversion rate, loss cost of additive elements, and complicated preparation process. achieve good crystallinity

Active Publication Date: 2021-01-26
INST OF PROCESS ENG CHINESE ACAD OF SCI
View PDF6 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The method of the present invention uses a cheap, non-toxic deep eutectic solvent to assist in the synthesis of the vanadyl phosphate catalyst, can prepare the vanadyl phosphate catalyst in an environmentally friendly manner, and can overcome the traditional reliance on noble metals to improve its performance, secondary pollution, high cost, and difficult preparation process Complicated and other disadvantages
When the catalyst is used to catalyze the reaction of n-butane selective oxidation to maleic anhydride, it improves the low yield of n-butane selective oxidation of maleic anhydride, catalyst selectivity, low conversion rate, loss of additive elements and cost in the prior art. advanced questions

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • A kind of vanadyl phosphate catalyst, its preparation method and application
  • A kind of vanadyl phosphate catalyst, its preparation method and application
  • A kind of vanadyl phosphate catalyst, its preparation method and application

Examples

Experimental program
Comparison scheme
Effect test

preparation example Construction

[0066] The embodiment of the present invention provides a kind of preparation method of vanadyl phosphate catalyst, it comprises the following steps:

[0067] S01: Put the vanadium source in a container, add a mixture of deep eutectic solvent: isobutanol: benzyl alcohol (volume ratio) = (0.15~0.25): (3~5): 1, and heat up to 100 ° C ~ 180 ℃ for 2 hours to 8 hours, then cooled to 30 ℃ to 80 ℃, then added phosphorus source, heated to 100 ℃ to 200 ℃ to continue the reaction for 10h to 24h, and the product was filtered, washed and dried to obtain the vanadyl phosphate precursor. The molar ratio of the phosphorus in the phosphorus source and the vanadium in the vanadium source is (0.8~1.5): 1, and the concentration of the described vanadium pentoxide in isobutanol and benzyl alcohol mixed solution is 0.02g / mL~0.12g / mL mL, the mass ratio of the vanadium source to the deep eutectic solvent is (50~10):1

[0068] S02: Calcining the vanadyl phosphate precursor at a temperature of 350° C...

Embodiment 1

[0077] (1) Weigh 15g V 2 o 5 Place in a 250mL three-necked flask, add a mixture of 1.5g polyethylene glycol-thiourea deep eutectic solvent, 80mL isobutanol and 20mL benzyl alcohol, stir and mix evenly, reflux at 135°C for 3 hours and then cool to 60°C ℃.

[0078] (2) Slowly add 11.29mL of 85% H 3 PO 4 , and continued to reflux for 16 hours at a temperature of 135° C. Filter and wash with absolute ethanol to obtain a blue precipitate, and dry it in air at 120° C. for 24 hours to obtain a vanadyl phosphate catalyst precursor powder.

[0079] (3) The obtained vanadyl phosphate catalyst precursor powder was pressed into tablets under a pressure of 15 MPa, crushed, and 20-40 mesh catalyst particles were sieved.

[0080] (4) Afterwards, the catalyst particles were activated in situ from room temperature to 430°C at a rate of 2°C / min for 12 hours in an atmosphere of n-butane / oxygen / nitrogen reaction gas with a volume ratio of 1.5:17:81.5 to obtain phosphoric acid vanadyl cataly...

Embodiment 2

[0084] (1) Weigh 15g V 2 o 5 Place in a 250mL three-neck flask, add a mixture of 1.5g polyethylene glycol-urea deep eutectic solvent, 80mL isobutanol and 20mL benzyl alcohol, stir and mix evenly, reflux at 135°C for 3 hours and then cool down to 60°C .

[0085] (2) Slowly add 11.29mL of 85% H 3 PO 4 , and continued to reflux for 16 hours at a temperature of 135° C. Filter and wash with absolute ethanol to obtain a blue precipitate, and dry it in air at 120° C. for 24 hours to obtain a vanadyl phosphate catalyst precursor powder.

[0086] (3) The obtained vanadyl phosphate catalyst precursor powder was pressed into tablets under a pressure of 15 MPa, crushed, and 20-40 mesh catalyst particles were sieved.

[0087] (4) Afterwards, the catalyst particles were activated in situ from room temperature to 430° C. at a rate of 2° C. / min under a reaction gas atmosphere for 12 hours to obtain a vanadyl phosphate catalyst.

[0088] Detection:

[0089] Take by weighing vanadyl phos...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

PUM

PropertyMeasurementUnit
specific surface areaaaaaaaaaaa
specific surface areaaaaaaaaaaa
Login to view more

Abstract

The invention relates to a vanadyl phosphate catalyst, its preparation method and application. The method comprises: 1) mixing and reacting a vanadium source, a deep eutectic solvent and an alcohol; 2) mixing the obtained product with a phosphorus source, raising the temperature to a temperature higher than the melting point of the deep eutectic solvent, continuing the reaction to obtain a precursor, and roasting , to obtain the vanadyl phosphate catalyst; the deep eutectic solvent is any one or at least two of urea-polyethylene glycol, urea-metal chloride, urea-choline chloride, or thiourea-polyethylene glycol A combination of species; the alcohol is benzyl alcohol, or C 3 ~C 8 A mixture of monohydric alcohols and benzyl alcohol. The method overcomes the shortcomings of the vanadyl phosphate catalyst relying on noble metals to improve its performance, causing secondary pollution, high cost, and complicated preparation process. When the vanadyl phosphate catalyst is used to catalyze the selective oxidation of n-butane to maleic anhydride, it overcomes the problems of low yield and poor selectivity, and overcomes the shortcomings of high cost and large pollution in traditional catalyst improvement methods.

Description

technical field [0001] The invention belongs to the field of chemical catalysis, and relates to a vanadyl phosphate catalyst, a preparation method and application thereof, in particular to a vanadyl phosphate catalyst, a preparation method enhanced by a deep eutectic solvent and an application thereof. Background technique [0002] The vanadyl phosphate catalyst is a composite metal oxide catalyst composed of V, P, and O. Due to its special structure, it can selectively oxidize butane to generate maleic anhydride. It is also the only catalyst that can catalyze this reaction. The crystal phase composition of the catalyst is very complex, and there are many crystal phases with different properties and compositions. It is reported in the literature that VOPO 4 2H 2 O, α Ⅰ -VOPO 4 、α Ⅱ -VOPO 4 , β-VOPO 4 , γ-VOPO 4 、VOHPO 4 0.5H 2 O. (VO) 2 P 2 o 7 Wait. Different crystal phases will affect the acid strength and microscopic morphology of the VPO catalyst, which in t...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Application Information

Patent Timeline
no application Login to view more
Patent Type & Authority Patents(China)
IPC IPC(8): B01J27/198B01J37/03B01J37/08C07D307/60
CPCB01J27/198B01J37/0018B01J37/031B01J37/08C07D307/60
Inventor 张锁江刘瑞霞张瑞锐贺滨代飞陈雪景李自航
Owner INST OF PROCESS ENG CHINESE ACAD OF SCI
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products