Unlock instant, AI-driven research and patent intelligence for your innovation.

A kind of catalyst for synthesizing isobutanol from synthesis gas, preparation method and application

A catalyst and synthesis gas technology, applied in the direction of catalyst activation/preparation, organic compound preparation, physical/chemical process catalyst, etc., can solve the problems of low carbon utilization rate, harsh reaction conditions, high selectivity, etc., to achieve increased utilization rate, Avoid waste, compose simple effects

Active Publication Date: 2019-04-02
SHANXI INST OF COAL CHEM CHINESE ACAD OF SCI
View PDF7 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0008] The above studies show that the synthesis of isobutanol from syngas has harsh reaction conditions, complex composition of alcohol products, low selectivity of total alcohol, CO 2 High selectivity, low carbon utilization, and low content of isobutanol in the product

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

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0026] Weigh 20.1g Zn(NO 3 ) 2 ·6H 2 O, 50.5g Cr(NO 3 ) 3 9H 2 After O was mixed with 200ml deionized water, it was heated to 35°C and mechanically stirred for 2h to prepare mixed solution A. Mix 45.2g of citric acid, 8.5g of silicotungstic acid and 200ml of deionized water, heat to 35°C, and mechanically stir for 2 hours to prepare mixed solution B. A peristaltic pump was used to adjust the dropping rate to 30ml / min, and the above-mentioned B solution was added dropwise to the above-mentioned A solution to obtain a sol-like solution. Seal the sol-like solution and age it at room temperature for 24 hours, then mechanically stir it at 70°C for 2 hours to evaporate the solvent for further gelation, and finally place it in an oven for 5 hours at 60°C, then heat it up to 100°C for 5 hours, then dry it in a muffle furnace at 200°C for 5 hours Afterwards, the temperature was raised to 400° C. and dried for 5 h to obtain powdery solid C.

[0027] Weigh 1.4g KNO 3 Make a solut...

Embodiment 2

[0030] Weigh 31.2g Zn(CH 3 COO) 2 2H 2 O, 29.6g Cr(CH 3 COO) 3 Prepare mixed solution A with 400ml deionized water, heat to 50°C, and mechanically stir for 4h. Take 48.1g of citric acid, 9.2g of silicotungstic acid and 400ml of deionized water to prepare a mixed solution B, heat it to 50°C, and stir it mechanically for 4h. A peristaltic pump was used to adjust the dropping rate to 25ml / min, and the above solution B was added dropwise to the above solution A to obtain a sol-like solution. After aging the above solution at room temperature for 30 hours, mechanically stir at 70°C for 2 hours to evaporate the solvent to further form a gel, and finally place it in an oven for 10 hours at 70°C, then raise the temperature to 110°C for 10 hours, and then dry it in a muffle furnace at 200°C for 5 hours. The temperature was raised to 400° C. and dried for 5 h to obtain powdery solid C.

[0031] Weigh 0.8g K 2 CO 3 Dissolve it in an appropriate amount of deionized water to make a...

Embodiment 3

[0034] Weigh 22.1g Zn(NO 3 ) 2 ·6H 2 O, 54.4g Cr(NO 3 ) 3 9H 2 O and 200ml of absolute ethanol were prepared as a mixed solution A, heated to 45°C, and mechanically stirred for 2h. Take 31.6g of oxalic acid, 7.4g of silicotungstic acid and 200ml of absolute ethanol to prepare a mixed solution B, heat it to 45°C, and stir it mechanically for 2h. A peristaltic pump was used to adjust the dropping rate to 20ml / min, and the above solution B was added dropwise to the above solution A to obtain a sol-like solution. After aging the above solution at room temperature for 48 hours, mechanically stir at 70°C for 2 hours to evaporate the solvent to form a gel, and finally place it in an oven for 5 hours at 60°C, then heat it up to 100°C for 5 hours, and then dry it in a muffle furnace at 200°C for 5 hours. The temperature was raised to 400° C. and dried for 5 h to obtain powdery solid C.

[0035] Weigh 0.7g KNO 3 Make a solution with an appropriate amount of deionized water, add ...

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

No PUM Login to View More

Abstract

The invention discloses a catalyst for synthesizing isobutyl alcohol from synthesis gas. The catalyst consists of the following components in percentage by weight: 10.0-45.0% of zinc oxide, 30.0-65.0% of chromium oxide, 5.0-20.0% of tungsten oxide, 0.1-0.4% of silicon dioxide and 1.0-5.0% of potassium oxide. The catalyst has the advantages of being low in CO2 selectivity, high in total alcohol and isobutyl alcohol selectivity and mild in reaction condition.

Description

technical field [0001] The invention relates to a catalyst for synthesizing isobutanol and a preparation method thereof, in particular to a catalyst for synthesizing isobutanol from synthesis gas, a preparation method and an application thereof. Background technique [0002] my country's energy structure is rich in coal, poor in oil, and low in gas. The energy structure dominated by coal will not change for a long time to come. So far, the utilization rate of coal is low, pollutant emissions are serious, limited carbon resources are wasted, and serious environmental pollution is caused. Therefore, it is imperative to develop green and efficient ways of coal utilization. [0003] Isobutanol is a basic organic chemical raw material, which can be used to manufacture isobutyl acetate (paint solvent), antioxidant 2,6-di-tert-butyl p-cresol, artificial musk, fruit essential oil, isobutyl isobutyrate (food flavor), isobutyl lactate, isobutyl butyrate, isobutyronitrile (fine chemic...

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): B01J23/30B01J37/03C07C29/153C07C31/12
CPCB01J23/002B01J23/30B01J37/036B01J2523/00C07C29/153B01J2523/13B01J2523/27B01J2523/41B01J2523/67B01J2523/69C07C31/12
Inventor 谭猗生贺久长高晓峰王军峰解红娟高俊文张涛武应全潘俊轩李小丽
Owner SHANXI INST OF COAL CHEM CHINESE ACAD OF SCI