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

Synthesis method of linear alkylbenzene

A technology of straight-chain alkyl benzene and synthesis method, applied in chemical instruments and methods, hydrocarbons, hydrocarbons, etc., can solve the problems of short single-pass life, easy deactivation of catalysts, etc., and achieve good activity stability, olefinic High conversion rate and low energy consumption

Inactive Publication Date: 2006-11-29
ZHEJIANG UNIV OF TECH
View PDF2 Cites 10 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] Although the solid acid alkylation process overcomes the shortcomings of the traditional hydrofluoric acid process, the current solid acid catalyst is prone to deactivation and has a short single-pass life. The solid acid process requires frequent switching operations between alkylation reaction and catalyst regeneration

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

[0030] The synthesis method provided by the present invention is used to synthesize the niobium phosphorus aluminum molecular sieve, which is denoted as C-1.

[0031] According to the molar ratio of raw materials is Al 2 o 3 :P 2 o 5 : Nb 2 o 5 :TPPA:ETHA:OXAA:H 2 O is calculated as 1: 0.660: 0.152: 0.802: 4.705: 0.121: 46.507, weigh 20 grams of monohydrate alumina, and 20 grams of phosphoric acid (H 3 PO 4 , 85Wt%), 7.8 grams of niobic acid, 15.1 grams of tri-n-propylamine (TPPA), 28.5 grams of ethanol (ETHA), 2 grams of oxalic acid (OXAA), and 110 grams of deionized water to prepare a mixed solution, stir well and place in crystal crystallization at 150°C for 3 days in a reaction kettle; then filtered, washed, dried, and calcined at 550°C for 5 hours to obtain anhydrous chemical composition (Nb 0.084 Al 0.552 P 0.364 )O 2 The niobium phosphorus aluminum molecular sieve, the X-ray powder diffraction experiment results are shown in Table 1, and its spectrum characte...

Embodiment 2

[0036] Using the synthesis method provided by the present invention, a magnesium-niobium-phosphorus-aluminum molecular sieve containing magnesium-substituting elements is synthesized, which is denoted as C-2.

[0037] According to the molar ratio of raw materials Al 2 o 3 :P 2 o 5 : Nb 2 o 5 :MgO:TPPA:ETHA:OXAA:H 2 O is 1: 0.541: 0.038: 0.227: 0.758: 2.353: 0.061: 27.482 calculation, weigh 40 grams of monohydrate alumina, and 32.8 grams of phosphoric acid (H 3 PO 4 , 85Wt%), 3.9 gram niobic acid, 12.8 gram magnesium acetate, 28.5 gram tri-n-propylamine (TPPA), 28.5 gram ethanol (ETHA), 2 gram oxalic acid (OXAA), 130 gram deionized water, prepare mixed solution, stir After uniformity, place it in a crystallization reaction kettle and crystallize at 150°C for 3 days; then filter, wash, dry, and roast at 550°C for 5 hours to obtain anhydrous chemical composition (Mg 0.067 Nb 0.022 Al 0.591 P 0.320 )O 2 The magnesium-niobium-phosphorus-aluminum molecular sieve substitu...

Embodiment 3

[0040] The boron-niobium-phosphorus-aluminum molecular sieve containing boron substituting elements is synthesized by adopting the synthesis method provided by the present invention, which is denoted as C-3.

[0041] According to the molar ratio of raw materials Al 2 o 3 :P 2 o 5 : Nb 2 o 5 :B 2 o 3 :TPPA:ETHA:OXAA:H 2 O is 1: 0.432: 0.038: 0.191: 0.756: 2.352: 0.304O: 25.368 calculation, weigh 40 grams of monohydrate alumina, and 26.2 grams of phosphoric acid (H 3 PO 4 , 85Wt%), 3.9 grams of niobic acid, 6.2 grams of boric acid, 28.5 grams of tri-n-propylamine (TPPA), 28.5 grams of ethanol (ETHA), 10 grams of oxalic acid (OXAA), 120 grams of deionized water, prepare a mixed solution, stir well Afterwards, it was placed in a crystallization reactor and crystallized at 150°C for 3 days; then filtered, washed, dried, and roasted at 550°C for 5 hours to obtain anhydrous chemical composition (B 0.115 Nb 0.023 Al 0.602 P 0.260 )O 2 The boron-niobium-phosphorus-aluminu...

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 process for preparing straight-chain alkylbenzene from C2-C20 straight-chain olefine and benzene features the alkylating reaction between benzene and olefine in the ratio of (2-100):1 in supercritical condition (290-450 deg.C and 5-15 MPa) under the action of solid acid catalyst. Said catalyst is the P-Al molecular sieve with AIPO4-5 crystal structure or the P-Al molecular sieve composition containing substitute element.

Description

(1) Technical field [0001] The invention relates to a method for synthesizing straight-chain alkylbenzenes, in particular to a method for synthesizing straight-chain alkylbenzenes using solid acid as a catalyst. (2) Background technology [0002] Linear alkylbenzene is the alkylation product of linear olefins and benzene under the action of a catalyst, and is the sulfonation raw material for the production of linear alkylbenzene sulfonate sodium detergent. The hydrofluoric acid-catalyzed alkylation process is widely used in industry to synthesize linear alkylbenzenes. Because hydrofluoric acid corrodes equipment, pollutes the environment, and is difficult to separate from alkylation products, non-corrosive, non-toxic solid acid catalysts are used instead of hydrofluoric acid catalysts, and linear alkylbenzenes are synthesized by environmentally friendly alkylation processes. become an inevitable development trend. [0003] CN1072353A discloses the use of Y-type molecular s...

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): C07C15/107C07C2/66B01J29/89B01J29/83
CPCY02P20/54
Inventor 任杰金辉黄国文
Owner ZHEJIANG UNIV OF TECH
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