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

Hydrogenation catalyst for producing cyclohexylamine from aniline

A technology of hydrogenation catalyst and cyclohexylamine, applied in the direction of catalyst activation/preparation, physical/chemical process catalyst, heterogeneous catalyst chemical elements, etc., can solve the problems of low selectivity and low yield of cyclohexylamine, etc. To achieve the effect of outstanding technical effect

Active Publication Date: 2022-04-05
CHINA PETROLEUM & CHEM CORP +1
View PDF4 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0007] One of the technical problems to be solved by the present invention is the problem of low yield and low selectivity of cyclohexylamine, and a new hydrogenation catalyst for producing cyclohexylamine from aniline is provided, and the method has the advantages of high yield of cyclohexylamine and high selectivity

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
  • Hydrogenation catalyst for producing cyclohexylamine from aniline
  • Hydrogenation catalyst for producing cyclohexylamine from aniline
  • Hydrogenation catalyst for producing cyclohexylamine from aniline

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0051] Modified carrier P / Al 2 o 3 Preparation of:

[0052] (1) Phosphoric acid (H 3 PO 4 ) aqueous solution 180ml impregnated in 1L diameter 6mm, pore volume is 0.92cm 3 / g, the specific surface area is 200cm 2 / g Al 2 o 3 , standing for 24 hours, and drying at 110° C. for 4 hours to obtain the carrier precursor I.

[0053] (2) Calcining the carrier precursor I at 630°C for 5h under a nitrogen gas atmosphere to obtain the modified carrier P / Al 2 o 3 .

[0054] The P content in the carrier was determined to be 1.50 g / L by ICP.

[0055] Preparation of hydrogenation catalyst:

[0056] (i) Cobalt ammonium sulfate containing 2.28g Co ((NH 4 ) 2 Co(SO 4 ) 2 ·6H 2 O) and calcium acetate containing 1.66g Ca (Ca(OAc) 2 ·H 2 O) 200ml of aqueous solution impregnated in P / Al 2 o 3 , to obtain catalyst precursor I;

[0057] (ii) drying at 110° C. for 4 hours to obtain the catalyst.

[0058] The Co content of the catalyst measured by ICP is 2.28g / L, and the Ca content...

Embodiment 2

[0063] Modified carrier P / Al 2 o 3 Preparation of:

[0064] (1) Phosphoric acid (H 3 PO 4 ) aqueous solution 180ml impregnated in 1L diameter 6mm, pore volume is 0.92cm 3 / g, the specific surface area is 200cm 2 / g Al 2 o 3 , standing for 24 hours, and drying at 110° C. for 4 hours to obtain the carrier precursor I.

[0065] (2) Calcining the carrier precursor I at 630°C for 5h under a nitrogen gas atmosphere to obtain the modified carrier P / Al 2 o 3 .

[0066] The P content in the carrier was determined to be 1.50 g / L by ICP.

[0067] Preparation of hydrogenation catalyst:

[0068] (i) Cobalt ammonium sulfate containing 2.28g Co ((NH 4 ) 2 Co(SO 4 ) 2 ·6H 2 O) and ammonium tetrachloroaurate ((NH 4 )AuCl 4 ·3H 2 O) 200ml of aqueous solution impregnated in P / Al 2 o 3 , to obtain catalyst precursor I;

[0069] (ii) drying at 110° C. for 4 hours to obtain the catalyst.

[0070]The Co content of the catalyst was measured by ICP to be 2.28g / L, and the Au cont...

Embodiment 3

[0099] Modified carrier P / Al 2 o 3 Preparation of:

[0100] (1) Ammonium phosphate (NH 4 ) 3 PO 4 ) aqueous solution 180ml impregnated in 1L diameter 6mm, pore volume is 0.92cm 3 / g, the specific surface area is 200cm 2 / g Al 2 o 3 , standing for 24 hours, and drying at 110° C. for 4 hours to obtain the carrier precursor I.

[0101] (2) Calcining the carrier precursor I at 630°C for 5h under a nitrogen gas atmosphere to obtain the modified carrier P / Al 2 o 3 .

[0102] The P content in the carrier was determined by ICP to be 0.80 g / L.

[0103] Preparation of hydrogenation catalyst:

[0104] (i) Cobalt ammonium sulfate containing 2.28g Co ((NH 4 ) 2 Co(SO 4 ) 2 ·6H 2 O) and beryllium acetate (Be(OAc) containing 1.66g Be 2 ·H 2 O) be dissolved in hot water to obtain 200ml of impregnating solution and impregnate in P / Al 2 o 3 , to obtain catalyst precursor I;

[0105] (ii) drying at 110° C. for 4 hours to obtain the catalyst.

[0106] The Co content of the ...

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 relates to a hydrogenation catalyst for producing cyclohexylamine from aniline, which mainly solves the problem of low yield and selectivity of cyclohexylamine synthesized by catalytic hydrogenation of aniline in the prior art. A hydrogenation catalyst for the production of cyclohexylamine from aniline, including a carrier and an active component, the carrier being phosphorus-modified Al 2 o 3 , the active component comprises Co element and promotor element; The technical scheme of said promotor element comprising at least one metal element selected from group IB metals solves this problem better and can be used in the industrial production of cyclohexylamine middle.

Description

technical field [0001] The invention relates to a hydrogenation catalyst for producing cyclohexylamine from aniline. Background technique [0002] Cyclohexylamine, also known as hexahydroaniline and aminocyclohexane, is a colorless and transparent liquid with a strong fishy amine smell and is miscible with water and common organic solvents. It is an important organic chemical raw material and fine chemical intermediate, mainly used in rubber additives, food additives, anti-corrosion, papermaking, plastic processing and textile industries. [0003] Foreign production and application are mainly concentrated in western developed countries and regions. The main manufacturers include American Air Products Corporation, Celanese Corporation, German BASF Corporation, Bayer Corporation and other manufacturers of various sizes. However, in Europe, cyclohexylamine has been in short supply due to the limitation of hydrogen raw materials. The domestic production capacity of cyclohexyla...

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): B01J27/185B01J37/02B01J37/08C07C211/35C07C209/72
CPCC07C209/72B01J27/1853B01J37/0201B01J37/082B01J2523/00C07C211/35B01J2523/23B01J2523/31B01J2523/845B01J2523/19B01J2523/21B01J2523/22B01J2523/25
Inventor 查晓钟杨运信
Owner CHINA PETROLEUM & CHEM CORP