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

Preparing method for magnetic materials and application thereof

A magnetic material and magnetic separation technology, applied in the field of preparation of new magnetic catalytic materials, can solve the problems of unreusable catalyst, low catalytic activity, complex by-products, etc., and achieve easy treatment conditions, high catalytic rate, and simple preparation process. Effect

Active Publication Date: 2017-01-11
KUNMING UNIV OF SCI & TECH
View PDF1 Cites 4 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The traditional theoretical production method of isoamyl acetate is: under the action of a catalyst, acetic acid and isoamyl ester undergo an esterification reaction. The traditional catalyst is concentrated sulfuric acid. However, it has been proved by experiments that using concentrated sulfuric acid as a catalyst can easily cause carbonization. phenomenon, the by-products are extremely complex, difficult to separate, and concentrated sulfuric acid is severely corrosive to equipment, and metal oxides are used as catalysts, the catalytic activity is low, and the temperature required for the reaction is high; using FeCl 3 , ZnCl 2 As a catalyst, there are disadvantages that the catalyst cannot be reused and the production cost is high. Since the above-mentioned catalysts all have obvious defects, it is necessary to find a more suitable catalyst, using magnetic materials as catalysts, which can be recovered and regenerated magnetically. , used in the synthesis of isoamyl acetate and achieved good results

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

[0021] The preparation method of the magnetic material described in this embodiment specifically includes the following steps:

[0022] (1) Add 0.006mol of FeCl 3 .6H 2 O, 0.049mol of NaOAc (sodium acetate) and 0.005mol of Na 3 Cit (sodium citrate) was dissolved in 58mL of ethylene glycol, then stirred for 1h, added to the reaction kettle and heated to 200°C for 10h, cooled and separated by magnetic separation and repeatedly washed with deionized water to obtain Fe 3 o 4 nanoparticles;

[0023] (2) Fe obtained in step (1) 3 o 4 Nanoparticles were dispersed in the ethanol solution mixed with 50mL ethanol and 1mL water at a ratio of 0.8g / 51mL, ultrasonically treated for 30min, and then 1.7mL ammonia solution with a mass percentage concentration of 25% was added, and 1mL orthosilicon was added during continuous stirring. Ethyl acetate (TEOS) was continuously stirred at 50°C for 4h, separated by a magnet, washed three times with ethanol and deionized water, and then vacuum-d...

Embodiment 2

[0030] The preparation method of the magnetic material described in this embodiment specifically includes the following steps:

[0031] (1) Add 0.0061mol of FeCl 3 .6H 2 O, 0.050mol of NaOAc (sodium acetate) and 0.0053mol of Na 3 Cit (sodium citrate) was dissolved in 59mL of ethylene glycol, then stirred for 1.3h, added to the reaction kettle and heated to 190°C for 10h, after cooling, separated by magnetic separation and repeatedly washed with deionized water to obtain Fe 3 o 4 nanoparticles;

[0032] (2) Fe obtained in step (1) 3 o 4 Nanoparticles were dispersed in the mixed ethanol solution of 57mL ethanol and 3mL water at a ratio of 0.8g / 60mL, ultrasonically treated for 40min, and then 1.8mL ammonia solution with a concentration of 25% by mass was added, and 1.1mL was added during continuous stirring. Orthoethyl silicate (TEOS), continuously stirred at 55°C for 5h, separated by a magnet, washed three times with ethanol and deionized water, and then vacuum-dried at 55°C...

Embodiment 3

[0039] The preparation method of the magnetic material described in this embodiment specifically includes the following steps:

[0040] (1) Add 0.0062mol of FeCl 3 .6H 2 O, 0.051mol of NaOAc (sodium acetate) and 0.0056mol of Na 3 Cit (sodium citrate) was dissolved in 60mL of ethylene glycol, then stirred for 1.6h, added to the reaction kettle and heated to 196°C for 11h, separated by magnetic separation after cooling and repeatedly washed with deionized water to obtain Fe 3 o 4 nanoparticles;

[0041] (2) Fe obtained in step (1) 3 o 4 Nanoparticles were dispersed in a mixed ethanol solution of 65mL ethanol and 5mL water at a ratio of 0.85g / 70mL, ultrasonically treated for 50min, then 1.9mL ammonia solution with a concentration of 25% by mass was added, and 1.1mL was added during continuous stirring. Orthoethyl silicate (TEOS), continuously stirred at 55°C for 5h, separated by a magnet, washed three times with ethanol and deionized water, and then vacuum-dried at 58°C for...

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
specific surface areaaaaaaaaaaa
specific surface areaaaaaaaaaaa
Login to View More

Abstract

The invention discloses a preparing method for magnetic materials and application thereof, and belongs to the field of material preparing and catalyzing. According to the method, ferroferric oxide Nano particles are prepared through a solvothermal method, wherein ferroferric oxide is used as the core part, and spherical Silicon dioxide Nano particles with the characteristic of monodispersity are used to cover the surface of the ferroferric oxide. Through the principle of coupled reaction, chlorosulfonic acid is adopted as a modification reagent to carry out modification on the core part which is covered with the silicon dioxide. The chlorosulfonic acid carries out modification on the core structure so that the modified core structure can be connected to Sulfonyl and then used for selectively adsorbing Fe 3+. After all the processes, the target product is finally obtained. The prepared magnetic materials can be used as the catalyst for synthesis of isoamyl acetate, and has the advantages of high catalytic activity, good reusability, and non-corrosion to apparatus. Besides, the magnetic materials can be easy to recycle and reuse as the catalyst.

Description

technical field [0001] The invention discloses that the invention relates to a preparation method and application of a novel magnetic catalytic material, and belongs to the field of material preparation and catalysis. Background technique [0002] With the rapid development of science and technology, magnetic nanoparticles have gradually entered people's field of vision, and various magnetic materials have been prepared. Compared with other magnetic materials, magnetic ferroferric oxide is the most widely used because of its excellent magnetic properties. Energy and large specific surface area make it easier to modify. Magnetic ferroferric oxide nanoparticles can be synthesized by many methods, but ferroferric oxide obtained by solvothermal synthesis has a larger specific surface area and better dispersion. However, magnetic Fe3O4 is easily acidified under acidic conditions and easily oxidized in air. These disadvantages greatly reduce its practicability to prevent the oxida...

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): B01J27/02C07C67/08C07C69/14
CPCC07C67/08B01J27/02B01J35/33B01J35/613C07C69/14
Inventor 汤立红包双友李凯宁平张冬冬孙鑫郭惠斌朱婷婷金旭张秀英
Owner KUNMING UNIV OF SCI & 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