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

Novel catalytic process for arylamine aromatic hydrocarbon alkylation

A technology for the alkylation of arylamine aromatic hydrocarbons, which is applied in the field of new catalytic technology for alkylation of aromatic amine aromatic hydrocarbons, can solve the problems of poor heat transfer performance, achieve high service life, high activity service life, and improve the effect

Active Publication Date: 2021-01-15
JIANGSU FEIYA CHEM IND
View PDF4 Cites 2 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0008] Aiming at the problems existing in the prior art, the object of the present invention is to provide a novel catalytic process for the alkylation of aromatic amines and aromatic hydrocarbons, which can realize innovative introduction of novel catalysts on the basis of existing production processes, and the novel catalysts include molecular sieve catalysts And heat transfer catalytic fiber rods, molecular sieve catalysts use acidic centers formed by protonic acids and aprotic acids to attach to the surface of molecular sieves to form catalysts with high activity and long service life. They are used in fixed bed reactors. The reaction process and catalysts are fluorine-free and non-toxic Chlorine, and can be reused without backwashing, and the introduction of heat transfer catalytic fiber rods can improve the problem of poor heat transfer performance in fixed bed reactors, not only can achieve rapid heat conduction and uniform distribution, but also can reduce heat To trigger its own expansion and contraction action, thereby causing the flow of the reactant gas in a local area, and improving the effect of the catalytic reaction by extruding the gas in contact with the molecular sieve catalyst, so as to realize the efficient and continuous production of alkylbenzene

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
  • Novel catalytic process for arylamine aromatic hydrocarbon alkylation
  • Novel catalytic process for arylamine aromatic hydrocarbon alkylation
  • Novel catalytic process for arylamine aromatic hydrocarbon alkylation

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0043] see Figure 1-2 , a novel catalytic process for the alkylation of arylamine aromatic hydrocarbons, comprising the following steps:

[0044] S1. Add benzene and long-chain olefins into the dehydration tower in proportion, and enter the dryer for drying after reflux dehydration;

[0045] S2. The raw material after drying treatment is heated to 130° C. in a reaction heating furnace, and fully reacted in the alkylbenzene reactor under the catalysis of a new catalyst to obtain a reaction product;

[0046] S3, the reaction product enters the atmospheric pressure distillation in the debenzene tower to remove the unreacted benzene, and then recycles it;

[0047] S4. The reaction product after benzene removal is sequentially subjected to vacuum distillation in a light removal tower and a weight removal tower to remove light components and heavy components in the reaction product to obtain pure alkylbenzene.

[0048] The molar ratio of benzene and long-chain olefins in step S1 ...

Embodiment 2

[0058] see Figure 1-2 , a novel catalytic process for the alkylation of arylamine aromatic hydrocarbons, comprising the following steps:

[0059] S1. Add benzene and long-chain olefins into the dehydration tower in proportion, and enter the dryer for drying after reflux dehydration;

[0060] S2. The raw material after drying treatment is heated to 150° C. in a reaction heating furnace, and fully reacted in the alkylbenzene reactor under the catalysis of a new catalyst to obtain a reaction product;

[0061] S3, the reaction product enters the atmospheric pressure distillation in the debenzene tower to remove the unreacted benzene, and then recycles it;

[0062] S4. The reaction product after benzene removal is sequentially subjected to vacuum distillation in a light removal tower and a weight removal tower to remove light components and heavy components in the reaction product to obtain pure alkylbenzene.

[0063] The molar ratio of benzene and long-chain olefins in step S1 ...

Embodiment 3

[0069] see Figure 1-2 , a novel catalytic process for the alkylation of arylamine aromatic hydrocarbons, comprising the following steps:

[0070] S1. Add benzene and long-chain olefins into the dehydration tower in proportion, and enter the dryer for drying after reflux dehydration;

[0071] S2. The raw material after drying treatment is heated to 180°C in a reaction heating furnace, and fully reacted in the alkylbenzene reactor under the catalysis of a new catalyst to obtain a reaction product;

[0072] S3, the reaction product enters the atmospheric pressure distillation in the debenzene tower to remove the unreacted benzene, and then recycles it;

[0073] S4. The reaction product after benzene removal is sequentially subjected to vacuum distillation in a light removal tower and a weight removal tower to remove light components and heavy components in the reaction product to obtain pure alkylbenzene.

[0074] The molar ratio of benzene and long-chain olefins in step S1 is...

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 novel catalytic process for arylamine aromatic hydrocarbon alkylation, belongs to the technical field of chemical synthesis, and can realize innovative introduction of a novel catalyst. The novel catalyst comprises a molecular sieve catalyst and a heat transfer catalytic fiber rod, an acidic center formed by protonic acid and aprotic acid is attached to the surface of a molecular sieve to form the catalyst with high activity and long service life, the catalyst is applied to a fixed bed reactor, the reaction process and the catalyst are fluoride-free and chlorine-free,and repeated utilization can be realized without backwashing. The introduced heat transfer catalytic fiber rod can improve the problem of poor heat transfer performance in the fixed bed reactor, notonly can realize rapid conduction and uniform distribution of heat, but also can trigger expansion and contraction actions of the fiber rods by the heat, so that reactant gas flows in a local range, and the reaction efficiency is improved. The catalytic reaction effect is improved through contact of the extruded gas and the molecular sieve catalyst, so that efficient and continuous production of alkylbenzene is realized.

Description

technical field [0001] The invention relates to the technical field of chemical synthesis, in particular to a novel catalytic process for the alkylation of aromatic amines and aromatic hydrocarbons. Background technique [0002] High-carbon (C20-24) alkylbenzenes are obtained from C20-24α-olefins through the alkylation reaction of catalysts and benzene. Higher-carbon alkylbenzene is sulfonated with sulfur trioxide to obtain higher-carbon alkylbenzenesulfonic acid (HLABS), and then undergoes neutralization and carbonation process to obtain higher-carbon alkylbenzenesulfonate calcium (HLABS-Ca). [0003] Calcium high-carbon alkylbenzene sulfonate is a kind of lubricant detergent, mainly used in the production of detergent T106. T106 has good high temperature thermal stability, oil solubility, anti-foaming property and water resistance. High alkali value, strong acid neutralization ability, good detergency and rust resistance. It is mainly used to prepare marine oil, medium ...

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 Applications(China)
IPC IPC(8): C07C2/66C07C7/04C07C15/107B01J29/76B01J37/02
CPCC07C2/66C07C7/04B01J29/76B01J37/0201C07C2529/76B01J35/33C07C15/107Y02P20/52
Inventor 张健雄王忠冬熊畅黄新晟储巍巍
Owner JIANGSU FEIYA CHEM IND
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