Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Pyridyl rhodium catalyst and its preparation method and application

A technology of pyridyl rhodium and catalyst, which is applied in the field of pyridyl rhodium catalyst and its preparation, can solve the problems of price change, lower conversion rate, and increase cost, and achieve the effects of maintaining activity, high conversion rate, and improving stability

Active Publication Date: 2021-10-19
NINGXIA UNIVERSITY
View PDF7 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

But there are also some problems in the rhodium-iodine catalyst in the Monsanto process, the catalyst active center [Rh(CO) 2 I 2 ] – The interaction with HI in the system will form [Rh(CO) 2 I 3 H] – , [Rh(CO) 2 I 3 H] – Then react with HI to form [Rh(CO) 2 I 4 ] – Causes the price change of the active center of the catalyst
Therefore generally need to add the water of mass fraction 14-16% to accelerate [Rh(CO) 2 I 4 ] – To [Rh(CO) 2 I 2 ] – The conversion of the catalyst improves the stability of the catalyst and maintains the activity of the catalyst. However, a high content of water will lead to the occurrence of water-gas shift side reactions in the middle of the reaction system, the conversion rate will decrease, and the cost will be increased in the later product separation process.

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
  • Pyridyl rhodium catalyst and its preparation method and application
  • Pyridyl rhodium catalyst and its preparation method and application
  • Pyridyl rhodium catalyst and its preparation method and application

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0029] The pyridyl rhodium catalyst of this embodiment consists of pyridyl-containing compound 2,2'-bipyridine-3,3'-dicarboxylic acid and Rh 2 (CO) 4 Cl 2 Coordination formation, the structural formula of pyridyl rhodium catalyst is as follows:

[0030]

[0031] The preparation method of above-mentioned pyridyl rhodium catalyst comprises the following steps:

[0032] (1) Weigh Rh 2 (CO) 4 Cl 2 Soluble in CH 3 Solution A is obtained in OH solution, and Rh in solution A 2 (CO) 4 Cl 2 The molar concentration is 0.006mol / L;

[0033] (2) According to the molar ratio Rh 2 (CO) 4 Cl 2 : 2,2'-bipyridine-3,3'-dicarboxylic acid=1:2 Weigh 2,2'-bipyridine-3,3'-dicarboxylic acid, dissolve in CH 3 Obtain solution B in OH, the molar concentration of 2,2'-bipyridine-3,3'-dicarboxylic acid in solution B is 0.006mol / L;

[0034] (3) According to the molar ratio Rh 2 (CO) 4 x 2 : NaBPh 4 =1:2 weigh NaBPh 4 , soluble in CH 3 OH to get solution C, in solution C NaBPh 4 The mol...

example 2

[0046] The pyridyl rhodium catalyst of the present embodiment is composed of pyridyl-containing compound 3-methyl-2-pyridinecarboxylic acid and Rh 2 (CO) 4 Cl 2 Coordination formation, the structural formula of pyridyl rhodium catalyst is as follows:

[0047]

[0048] The preparation method of above-mentioned pyridyl rhodium catalyst comprises the following steps:

[0049] (1) Weigh Rh 2 (CO) 4 Cl 2 Soluble in CH 3 Solution A is obtained in OH solution, and Rh in solution A 2 (CO) 4 Cl 2 The molar concentration is 0.004mol / L;

[0050] (2) According to the molar ratio Rh 2 (CO) 4 Cl 2 : 3-methyl-2-pyridinecarboxylic acid=1:2 Weigh 3-methyl-2-pyridinecarboxylic acid, dissolve in CH 3 Solution B is obtained in OH, and the molar concentration of 3-methyl-2-pyridinecarboxylic acid in solution B is 0.004mol / L;

[0051] (3) According to the molar ratio Rh 2 (CO) 4 Cl 2 : NaBPh 4 =1:2 weigh NaBPh 4 , soluble in CH 3 OH to get solution C, in solution C NaBPh 4 T...

Embodiment 3

[0057] The pyridyl rhodium catalyst of the present embodiment is composed of pyridyl-containing compound methyl picolinate and Rh 2 (CO) 4 I 2 Coordination formation, the structural formula of pyridyl rhodium catalyst is as follows:

[0058]

[0059] The preparation method of above-mentioned pyridyl rhodium catalyst comprises the following steps:

[0060] (1) Weigh Rh 2 (CO) 4 I 2 Soluble in CH 3 Solution A is obtained in OH solution, and Rh in solution A 2 (CO) 4 I 2 The molar concentration is 0.008mol / L;

[0061] (2) According to the molar ratio Rh 2 (CO) 4 I 2 : 2,2'-bipyridine-3,3'-dicarboxylic acid=1:2 Weigh 2,2'-bipyridine-3,3'-dicarboxylic acid, dissolve in CH 3 Obtain solution B in OH, the molar concentration of 2,2'-bipyridine-3,3'-dicarboxylic acid in solution B is 0.008mol / L;

[0062] (3) According to the molar ratio Rh 2 (CO) 4 I 2 : NaBPh 4 =1:2 weigh NaBPh 4 , soluble in CH 3 OH to get solution C, in solution C NaBPh 4 The molar concentrat...

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

A kind of pyridyl rhodium catalyst, described pyridyl rhodium catalyst is made of pyridyl-containing compound and Rh 2 (CO) 4 x 2 Coordination formation, wherein, X is Cl or I. The present invention uses Rh 2 (CO) 4 x 2 With the compound raw material containing pyridyl group, Rh-N and Rh-O coordination bonds are formed between rhodium carbonyl and the compound containing pyridyl group, so that rhodium is coordinated with the compound containing pyridyl group, and a stable pyridine structure is obtained. rhodium-based catalysts. The pyridyl rhodium catalyst maintains the stability of the catalyst by containing pyridine groups, so that the catalyst is not easy to decompose and precipitate to cause deactivation, and the stability of the catalyst is improved by adding ligands on the basis of the rhodium-based catalyst to maintain its activity. In addition, in this reaction, methanol and CO are used as raw materials to synthesize acetic acid. In the reaction, not only the conversion rate of methanol is high, but also only acetic acid is selectively produced, which solves the problems of many by-products and low selectivity of acetic acid in the carbonylation process. The invention also provides the preparation method and application of the pyridyl rhodium catalyst.

Description

Technical field: [0001] The invention relates to the technical field of preparing acetic acid by carbonylation, in particular to a pyridyl rhodium catalyst and a preparation method and application thereof. Background technique: [0002] Acetic acid is an important basic organic chemical product. As an important organic raw material and an excellent organic solvent, it is widely used in industries such as chemical industry, light textile, plastic, medicine, rubber and dyestuff. [0003] At present, as far as the acetic acid production process in the world is concerned, the acetic acid production process of methanol carbonylation has become the global acetic acid production process, and the Monsanto production technology has also become the mainstream process of its acetic acid production. Monsanto production process is based on [Rh(CO) 2 I 2 ] – As the catalytic active center, the reaction conditions are 150-200°C, the pressure is 3-6MPa, and the reaction conditions are re...

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): C07F15/00B01J31/20B01J31/18C07C53/08C07C51/12
CPCB01J31/1815B01J31/20B01J2531/0238B01J2531/822C07C51/12C07F15/008C07C53/08
Inventor 吉文欣楚秀秀张莎莎马玉龙
Owner NINGXIA UNIVERSITY
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products