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

A kind of n-butene isomerization catalyst and preparation method thereof

A catalyst and isomerization technology, which are applied in the field of n-butene isomerization catalyst and preparation thereof, can solve the problems of complicated operation steps, single carrier pores, poor catalytic effect, etc., and achieve high catalytic activity, simple preparation method, Highly selective effect

Active Publication Date: 2018-04-10
CHINA PETROLEUM & CHEM CORP +1
View PDF5 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The above publications have adopted the negative pressure deposition precipitation method and the HZSM-5 molecular sieve carrier to prepare the supported gold catalyst, but the disadvantages of this method are that the operation steps are cumbersome, the carrier has a single channel, the cost is high, and the catalytic effect is not good.

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
  • A kind of n-butene isomerization catalyst and preparation method thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0032] 1) Preparation of SAPO-11 / SAPO-46 composite molecular sieve

[0033] Weigh 9.52 g (0.07 mol) of pseudo-boehmite, dissolve it in 10 g of deionized water to prepare a pseudo-boehmite aqueous solution, and stir for 0.5 h. 16.14g (0.14mol) of H 3 PO 4 (85% by weight in water) and stirred for another 1 h. Measure 4.78ml (0.035mol) of di-n-propylamine and add it dropwise to the above solution, and stir for 1h. Next, 10.08 g (0.042 mol) of silica sol was weighed and added to the above solution. Add water and stir for 1h to obtain a colloidal mixture, in which the number of moles of Al 2 o 3 :R:P 2 o 5 :SiO2 2 :H 2 O=1:0.5:1:0.6:50, wherein R is di-n-propylamine.

[0034] The colloidal mixture prepared above was aged at 80°C for 4h, then heated to 180°C, and hydrothermally crystallized under autogenous pressure for 22h. The crystallized product was cooled, washed by centrifugation, and then dried at 120°C for 12h. Obtain SAPO-11 / SAPO-46 composite molecular sieve, it...

Embodiment 2

[0041] 1) Preparation of SAPO-11 / SAPO-46 composite molecular sieve

[0042] Weigh 9.52 g (0.07 mol) of pseudo-boehmite, dissolve it in 10 g of deionized water to prepare a pseudo-boehmite aqueous solution, and stir for 0.5 h. 16.14g (0.14mol) of H 3 PO 4 (85% by weight in water) and stirred for another 1 h. Measure 7.64ml (0.056mol) of diisopropylamine and add it dropwise to the above solution, and stir for 1h. Next, 10.08 g (0.042 mol) of silica sol was weighed and added to the above solution. Add water and stir for 1h to obtain a colloidal mixture, in which the number of moles of Al 2 o 3 :R:P 2 o 5 :SiO2 2 :H 2 O=1:0.8:1:0.6:40, wherein R is diisopropylamine.

[0043] The colloidal mixture prepared above was aged at 100°C for 3h, then heated to 180°C, and hydrothermally crystallized under autogenous pressure for 12h. The crystallized product was cooled, washed by centrifugation, and then dried at 110° C. for 12 hours to obtain a SAPO-11 / SAPO-46 composite molecula...

Embodiment 3

[0050] 1) Preparation of SAPO-11 / SAPO-46 composite molecular sieve

[0051] Weigh 9.52 g (0.07 mol) of pseudo-boehmite, dissolve it in 10 g of deionized water to prepare a pseudo-boehmite aqueous solution, and stir for 0.5 h. 16.14g (0.14mol) of H 3 PO 4 (85% by weight aqueous solution), and then stirred for 1 h; weighed 14.3 ml (0.105 mol) of di-n-propylamine and added dropwise to the above solution, and stirred for 1 h. Next, 13.44 g (0.056 mol) of silica sol was weighed and added to the above solution. Add water and stir for 1h to obtain a colloidal mixture, in which the number of moles of Al 2 o 3 :R:P 2 o 5 :SiO2 2 :H 2 O=1:1.5:1:0.8:50, wherein R is di-n-propylamine.

[0052] The colloidal mixture prepared above was aged at 110°C for 4h, then heated to 180°C, and hydrothermally crystallized under autogenous pressure for 8h. The crystallized product was cooled, washed by centrifugation, and then dried at 120° C. for 6 h to obtain a SAPO-11 / SAPO-46 composite mole...

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 provides a n-butene isomerization catalyst, which comprises SAPO-11 / SAPO-46 composite molecular sieve with hierarchical pores as a carrier, and Group IB metals loaded on the carrier as an active component. The present invention also provides a preparation method for the above-mentioned catalyst, which includes preparing SAPO‑11 / SAPO‑46 composite molecular sieves by controlling the ratio of raw materials in the synthesis process, and adopting an appropriate crystallization method and crystallization temperature, and then loading IB group metals, making the catalyst a bifunctional catalyst with metal and acid centers. The preparation method is simple and convenient, has no environmental pollution and is suitable for industrial production. The catalyst provided by the invention has higher catalytic activity and higher isobutene selectivity when used for preparing isobutene through normal butene skeleton isomerization.

Description

technical field [0001] The invention relates to the field of olefin isomerization catalysts, in particular to a n-butene isomerization catalyst and a preparation method thereof. Background technique [0002] Isobutylene is an important organic chemical raw material, mainly used to produce methyl tert-butyl ether (MTBE), tert-butanol, butyl rubber, polyisobutylene, methyl methacrylate, tert-butyl mercaptan and other organic Chemical Products. In recent years, due to the sharp increase in the demand for isobutene, especially for the production of MTBE, an environmentally friendly gasoline additive, the demand for isobutene has grown rapidly around the world, and the isobutene output obtained by the traditional petroleum catalytic cracking process is far from meeting industrial needs. Therefore, Research and development of new technologies for isobutylene production have been carried out extensively at home and abroad. [0003] In the 1970s and 1980s, the n-butene isomerizati...

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): B01J29/85C07C11/09C07C5/25
Inventor 张利霞任行涛齐海英栗同林刘艳惠杨光裴庆君
Owner CHINA PETROLEUM & CHEM CORP