Supercharge Your Innovation With Domain-Expert AI Agents!

Method for synthesizing 1,4-butanediol

A technology of butanediol and diacetoxybutene, applied in chemical instruments and methods, preparation of organic compounds, preparation of oxygenated compounds, etc., can solve the problems of low yield and selectivity of 4-butanediol

Active Publication Date: 2019-10-11
CHINA PETROLEUM & CHEM CORP +1
View PDF3 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0006] The technical problem to be solved by the present invention is the problem of low yield and selectivity of 1,4-butanediol, and a new method for synthesizing 1,4-butanediol is provided, which has 1,4-butanediol Features of high alcohol yield 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
  • Method for synthesizing 1,4-butanediol
  • Method for synthesizing 1,4-butanediol
  • Method for synthesizing 1,4-butanediol

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0043] Preparation of hydrogenation catalyst:

[0044] ① Ammonium chloroplatinite ((NH 4 ) 2 PtCl 4 ) is dissolved in the hydrochloric acid aqueous solution that concentration is 8wt%, obtains impregnation solution 200ml, and 1L diameter 3mm, length 2cm, pore volume are 0.80cm 3 / g, the specific surface area is 1200cm 2 The coal-based cylindrical activated carbon carrier of / g is impregnated in the above-mentioned impregnating liquid, obtains catalyst precursor I;

[0045] ② Standing and aging for 24 hours to obtain catalyst precursor II;

[0046] ③ with a concentration of 8% (in N 2 h 4 ·H 2 The 500ml hydrazine hydrate of (2 weight ratio) reduces catalyst precursor II for 3h, obtains catalyst precursor III;

[0047] ④ washed with water to no chloride ion, dried at 50°C for 4 hours to obtain catalyst precursor IV;

[0048] ⑤ impregnating 180 ml of an aqueous solution of rubidium acetate (RbOAc) containing 2.10 g of Rb on the catalyst precursor IV, and drying at 110° C...

Embodiment 2

[0054] Preparation of hydrogenation catalyst:

[0055] ① Ammonium chloroplatinite ((NH 4 ) 2 PtCl 4 ) is dissolved in the hydrochloric acid aqueous solution that concentration is 8wt%, obtains impregnation solution 200ml, and 1L diameter 3mm, length 2cm, pore volume are 0.80cm 3 / g, the specific surface area is 1200cm 2 The coal-based cylindrical activated carbon carrier of / g is impregnated in the above-mentioned impregnating liquid, obtains catalyst precursor I;

[0056] ② Standing and aging for 24 hours to obtain catalyst precursor II;

[0057] ③ with a concentration of 8% (in N 2 h 4 ·H 2 The 500ml hydrazine hydrate of (2 weight ratio) reduces catalyst precursor II for 3h, obtains catalyst precursor III;

[0058] ④ washed with water to no chloride ion, dried at 50°C for 4 hours to obtain catalyst precursor IV;

[0059] ⑤ Zinc citrate containing 2.10g Zn (Zn 3 (C 6 h 5 o 7 ) 2 2H 2 O) 180ml of aqueous solution was impregnated on the catalyst precursor IV, and...

Embodiment 3

[0089] Preparation of hydrogenation catalyst:

[0090] ① Ammonium chloroplatinite ((NH 4 ) 2 PtCl 4 ) is dissolved in the hydrochloric acid aqueous solution that concentration is 8wt%, obtains impregnation solution 200ml, and 1L diameter 3mm, length 2cm, pore volume are 0.80cm 3 / g, the specific surface area is 1200cm 2 The coal-based cylindrical activated carbon carrier of / g is impregnated in the above-mentioned impregnating liquid, obtains catalyst precursor I;

[0091] ② Standing and aging for 24 hours to obtain catalyst precursor II;

[0092] ③ with a concentration of 8% (in N 2 h 4 ·H 2 The 500ml hydrazine hydrate of (2 weight ratio) reduces catalyst precursor II for 3h, obtains catalyst precursor III;

[0093] ④ washed with water to no chloride ion, dried at 50°C for 4 hours to obtain catalyst precursor IV;

[0094] ⑤The cadmium acetate containing 2.10g Cd (Cd(OA C ) 2 2H 2 O) Dissolved in an aqueous solution of 10 wt% acetic acid to obtain 180 ml of impregn...

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

PropertyMeasurementUnit
specific surface areaaaaaaaaaaa
Login to View More

Abstract

The invention relates to a method for synthesizing 1,4-butanediol and mainly aims to solve the problem that, in the prior art, 1,4-butanediol is poor in yield and selectivity after 1,4-diacetoxybutaneis hydrolyzed because 1,4-diacetoxy butylene is poor in yield and selectivity after hydrogenation. The method for synthesizing 1,4-butanediol comprises the following steps: by taking butadiene, butadiene and oxygen as raw materials, performing an acetylation reaction in the presence of an acetylation catalyst so as to obtain 1,4-diacetoxy butylene; in the presence of a hydrogenation catalyst, enabling hydrogen to react with 1,4-diacetoxy butylene so as to obtain 1,4-diacetoxybutane; hydrolyzing 1,4-diacetoxybutane, thereby obtaining 1,4-butanediol, wherein the hydrogenation catalyst comprisesactivated carbon as a carrier and active components including a Pt element and a promoter element; the promoter element comprises at least one metal element of IA group metals and at least one metalelement of IIB group metals.

Description

technical field [0001] The present invention relates to a method for synthesizing 1,4-butanediol. Background technique [0002] 1,4-Butanediol (1,4-BDO) is an important organic and fine chemical raw material, which is widely used in the fields of medicine, chemical industry, textile, papermaking, automobile and daily chemical industry. It can derive a series of high value-added fine chemical products. For example, tetrahydrofuran (THF), polybutylene terephthalate (PBT), γ-butyrolactone (GBL) and polyurethane resin (PU Resin) can be produced from 1,4-BDO, especially as the production of PBT engineering The basic raw material of plastic and PBT fiber has received extensive attention from research institutions. [0003] There are many process routes for the preparation of 1,4-butanediol. From the raw materials used, there are acetylene, ethylene, propylene, butadiene and maleic anhydride and other raw material routes. The same raw materials also have different synthesis proce...

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): C07C31/20C07C27/02B01J23/58B01J23/60B01J35/10
CPCC07C29/095C07C67/055C07C67/283B01J23/58B01J23/60B01J35/618B01J35/635C07C31/207C07C69/16
Inventor 查晓钟杨运信
Owner CHINA PETROLEUM & CHEM CORP
Features
  • R&D
  • Intellectual Property
  • Life Sciences
  • Materials
  • Tech Scout
Why Patsnap Eureka
  • Unparalleled Data Quality
  • Higher Quality Content
  • 60% Fewer Hallucinations
Social media
Patsnap Eureka Blog
Learn More