Preparation method of officinal nano-zinc oxide

A nano-zinc oxide and zinc hydroxide technology, applied in the field of medicine and chemical industry, can solve the problem of high organic solvent residue, and achieve the effects of reducing energy consumption, low reaction temperature and low temperature

Active Publication Date: 2015-08-19
HUNAN ER KANG PHARMA
View PDF4 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

This patented describes methods that use an enzyme called ZnH2O4 (Zinc Hydroxy Acid Oxo lyase) to break down zinc into smaller particles during heat treatment at temperatures between 107°C and 155°C. These tiny particles are then separated from other components before being further processed or packaged together. By doing these steps, it becomes possible to produce pure nanosilver without any impurities like carbons or metalloids.

Problems solved by technology

This patents describes different ways to make tiny metal oxides like zircone dioxygen or tinoxygen. However these techniques are limited because they require expensive equipment such as high pressure vessels and special chemical agents. There has been some research on producing small metallic zinc flakes without complicated processes involving multiple steps.

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
  • Preparation method of officinal nano-zinc oxide

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0024] 10kg of zinc hydroxide was powdered and ground, and 10kg of fatty acid glycerides and 60L of deionized water were added to the autoclave. Stir the reaction at 110°C and 20MPa for 2 hours. After the reaction is over, the obtained solution is ultrasonically washed for 30 minutes and the supernatant liquid is poured off. The obtained filter cake is washed with deionized water and ultrasonically for 30 minutes to remove the supernatant liquid. The obtained solid is ultrasonically washed with ethanol for 30 minutes and then used for nanofiltration Membrane filtration, the filter cake was then ultrasonically washed with deionized water for 30 min and filtered with a nanofiltration membrane. The solid obtained in the above steps was dried at 40° C. for 3 hours under a reduced pressure of 0.08 Mpa to obtain nano zinc oxide.

[0025] The particle size range of the obtained nanometer zinc oxide is 3-60 nanometers, and the product purity is 99.95%.

Embodiment 2

[0027] 15kg of zinc hydroxide was powdered and ground, and 30kg of fatty acid glycerides and 80L of deionized water were added to the autoclave. Stir and react at 130°C and 30MPa for 2 hours. After the reaction is over, the obtained solution is ultrasonically washed for 30 minutes and then the supernatant is poured off. The obtained filter cake is washed with deionized water and ultrasonically for 30 minutes to remove the supernatant. The obtained solid is ultrasonically washed with ethanol for 30 minutes and filtered through a nanofiltration membrane. 1. The filter cake was ultrasonically washed with deionized water for 30 min and filtered through a nanofiltration membrane. The solid obtained in the above steps was dried at 40° C. for 3 hours under a reduced pressure of 0.08 Mpa to obtain nano zinc oxide.

[0028] The particle size range of the obtained nanometer zinc oxide is 3-60 nanometers, and the product purity is 99.92%.

Embodiment 3

[0030] 10kg of zinc hydroxide was powdered and ground, and 25kg of fatty acid glycerides and 50L of deionized water were added to the autoclave. Stir and react at 140°C and 40MPa for 2 hours. After the reaction, the obtained solution is ultrasonically washed for 30 minutes, and then the supernatant is poured out. The obtained filter cake is washed with deionized water and ultrasonically for 30 minutes to remove the supernatant. The obtained solid is ultrasonically washed with ethanol for 30 minutes and filtered with a nanofiltration membrane. 1. The filter cake was ultrasonically washed with deionized water for 30 min and filtered through a nanofiltration membrane. The solid obtained in the above steps was dried at 40° C. for 3 hours under a reduced pressure of 0.08 Mpa to obtain nano zinc oxide.

[0031] The particle size range of the obtained nanometer zinc oxide is 3-60 nanometers, and the product purity is 99.91%.

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
Particle sizeaaaaaaaaaa
Particle sizeaaaaaaaaaa
Particle sizeaaaaaaaaaa
Login to view more

Abstract

The invention provides a preparation method of officinal nano-zinc oxide. Zinc hydroxide, a surfactant and deionized water are added into a high pressure reactor according to a certain proportion; stirring is performed under certain temperature for reaction; after the reaction is ended, obtained solution is subjected to suction filtration, deionized water washing, ethyl alcohol washing and deionized water washing, and is dried under a pressure reduction condition, thus obtaining the officinal nano-zinc oxide.

Description

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

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
Owner HUNAN ER KANG PHARMA
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products