CN107857290A - A kind of nano zine oxide - Google Patents
A kind of nano zine oxide Download PDFInfo
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- CN107857290A CN107857290A CN201711025032.7A CN201711025032A CN107857290A CN 107857290 A CN107857290 A CN 107857290A CN 201711025032 A CN201711025032 A CN 201711025032A CN 107857290 A CN107857290 A CN 107857290A
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Abstract
The present invention provides a kind of nano zine oxide, and its preparation method is specially to weigh zinc sulfate to be put into beaker, adds deionized water, beaker is placed on magnetic stirring apparatus, stir at room temperature to being completely dissolved, then ammonium carbonate is added into above-mentioned solution, centrifuge to obtain white depositions Zn5(CO3)2(OH)6；Above-mentioned sediment is poured into three-necked flask, magnetic agitation, vacuumize, mixed liquor is to 120 DEG C in electric jacket heating there-necked flask, absolute ethyl alcohol 50mL is added into obtained mixture, through centrifuging to obtain sediment, washed again with absolute ethyl alcohol 60mL, centrifugation, dry, obtain nano zine oxide raw material, the nano zine oxide can improve existing Particle Size of Nanometer ZnO it is big, than surface minor issue, so as to improve its specific surface area and chemism, and then improve it and be widely used in the industries such as rubber, medicine, chemical industry, light industry.
Description
The present patent application is application number CN201610531007.5, the applying date 2016 year 07 month 07 day, and denomination of invention is " a kind of
The divisional application of nano zine oxide preparation method ".
Technical field
The present invention relates to a kind of nano zine oxide and preparation method thereof, belong to technical field of inorganic material.
Background technology
Nano zine oxide is a kind of multi-functional new inorganic material, and its granular size is about at 1~100 nanometer.Due to
The granular of crystal grain, its Electronic Structure and crystal structure change, and generate the surface effect that macro object does not have
Should, bulk effect, quantum size effect and the features such as macroscopical tunnel-effect and the high grade of transparency, polymolecularity.Discovered in recent years
It shows many specific functions in catalysis, optics, magnetics, mechanics etc., makes it in ceramics, chemical industry, electronics, optics, life
There is important application value in many fields such as thing, medicine, have particularity and purposes that common zinc oxide can not compare.Nanometer
Zinc oxide can be used for ultraviolet light masking material, antiseptic, fluorescent material, catalysis material etc. in fields such as weaving, coating.Due to
The a series of superiority of nano zine oxide and very tempting application prospect, therefore research and development nano zine oxide turns into many science and technology
Personnel's focus of attention.
At present, the method for preparing nano zinc oxide material has many kinds, such as vapour deposition process, colloidal sol-gel method, precipitation
Method, combustion method, water（Solvent）Hot method, template etc..Obtained zinc oxide nano rod material diameter is thicker, specific surface area compared with
Small, size heterogeneity, dispersiveness is also not good enough, have impact on the application performance of nano zine oxide nanometer.
Compared with above-mentioned synthetic method, then it is more easy to obtain that pattern is homogeneous, dispersiveness high is received using oil phase thermolysis process
Rice material, the method technique of oil phase thermal decomposition is simple, and reaction time is short, and yield is high, is adapted to scale ZnO nano material.
The content of the invention
This method can solve the problems, such as that the big particle diameter of nano zine oxide, bad dispersibility, draw ratio are small, compare table so as to improve it
Area and chemism, and then improve it and be widely used in the industries such as rubber, medicine, chemical industry, light industry.
1, which weighs zinc sulfate 0.14g, is put into 500mL beakers, adds 40g deionized waters, beaker is placed in into magnetic stirring apparatus
On, stir at room temperature to being completely dissolved, then 0.12g ammonium carbonates are added into above-mentioned solution, stirring is to reacting complete at room temperature,
Centrifuge to obtain white depositions Zn5(CO3)2(OH)6；Above-mentioned sediment is poured into 250mL three-necked flasks, takes 5g Adipoyl Chlorides, ethene
Ethyl triethoxy silicane alkane 2g, butyl acrylate 3g and 2- phosphonobutane -1,2,4- tricarboxylic acids sodium salts 0.2g add there-necked flask, magnetic force
Stirring, is vacuumized, and mixed liquor is to 120 DEG C in electric jacket heating there-necked flask, and is incubated 60min；Protected in magnetic agitation and nitrogen
Under, the rapid mixed solution that heats is incubated 60min to 300 DEG C, then naturally cools to room temperature, adds into obtained mixture
Enter absolute ethyl alcohol 50mL, through centrifuging to obtain sediment, washed again with absolute ethyl alcohol 60mL, centrifuged, dry, obtain nano zine oxide
Raw material.
2, which weigh zinc sulfate 0.24g, is put into beaker, adds 60g deionized waters, beaker is placed on magnetic stirring apparatus,
Stirring at room temperature to being completely dissolved, then 0.20g potassium carbonate is added into above-mentioned solution, magnetic agitation is to reacting complete at room temperature,
Centrifuge to obtain white depositions Zn5(CO3)2(OH)6；Above-mentioned sediment is poured into three-necked flask, takes 2g oxalyl chlorides, the second of vinyl three
TMOS 2g, ethyl acrylate 8g and hydroxy ethylene diphosphonic acid 0.3g add there-necked flask, magnetic agitation, vacuumize, and utilize
Mixed liquor is to 160 DEG C in electric jacket heating there-necked flask, and is incubated 30min；Under magnetic agitation and nitrogen protection, rapid heating is mixed
Solution is closed to 280 DEG C, and is incubated 90min, room temperature is then naturally cooled to, absolute ethyl alcohol is added into obtained mixture, is passed through
Sediment is centrifuged to obtain, is washed again with absolute ethyl alcohol, is centrifuged, dries, obtains nano zine oxide.
3, which weigh zinc sulfate 0.34g, is put into beaker, adds 60g deionized waters, beaker is placed on magnetic stirring apparatus,
Stirring at room temperature to being completely dissolved, then 0.20g potassium carbonate is added into above-mentioned solution, magnetic agitation is to reacting complete at room temperature,
Centrifuge to obtain white depositions Zn5(CO3)2(OH)6；Above-mentioned sediment is poured into three-necked flask, measures 2g chlorobenzoyl chlorides, vinyl
Triethoxysilane 2g, hydroxy-ethyl acrylate 8g add there-necked flask, magnetic agitation, vacuumize, and there-necked flask is heated using electric jacket
Interior mixed liquor is incubated 30min to 160 DEG C；Under magnetic agitation and nitrogen protection, mixed solution is heated rapidly to 280 DEG C, and
90min is incubated, room temperature is then naturally cooled to, absolute ethyl alcohol is added into obtained mixture, through centrifuging to obtain sediment, again
Washed, centrifuged with absolute ethyl alcohol, dried, obtain nano zine oxide.
4, which weigh zinc sulfate 0.42g, is put into beaker, adds 70g deionized waters, beaker is placed on magnetic stirring apparatus, room
The lower stirring of temperature is to being completely dissolved, then 0.20g potassium carbonate is added into above-mentioned solution, and magnetic agitation is to reacting complete at room temperature, from
Gains in depth of comprehension white depositions Zn5(CO3)2(OH)6；Above-mentioned sediment is poured into three-necked flask, takes 2g stearic acid chlorides, the second of vinyl three
TMOS 2g, hydroxyethyl methacrylate 8g add there-necked flask, magnetic agitation, vacuumize, and there-necked flask is heated using electric jacket
Interior mixed liquor is incubated 30min to 160 DEG C；Under magnetic agitation and nitrogen protection, mixed solution is heated rapidly to 280 DEG C, and
90min is incubated, room temperature is then naturally cooled to, absolute ethyl alcohol is added into obtained mixture, through centrifuging to obtain sediment, again
Washed, centrifuged with absolute ethyl alcohol, dried, obtain nano zine oxide.
5, which weigh zinc sulfate 0.26g, is put into beaker, adds 80g deionized waters, beaker is placed on magnetic stirring apparatus,
Stirring at room temperature to being completely dissolved, then 0.20g potassium carbonate is added into above-mentioned solution, magnetic agitation is to reacting complete at room temperature,
Centrifuge to obtain white depositions Zn5(CO3)2(OH)6；Above-mentioned sediment is poured into three-necked flask, measures 2g heptadecanes acyl chlorides, ethene
Ethyl triethoxy silicane alkane 2g and itaconic acid 8g adds there-necked flask, magnetic agitation, vacuumizes, and is heated in there-necked flask and mixed using electric jacket
Liquid is closed to 160 DEG C, and is incubated 30min；Under magnetic agitation and nitrogen protection, the rapid mixed solution that heats is incubated to 280 DEG C
90min, room temperature is then naturally cooled to, absolute ethyl alcohol 60g is added into obtained mixture, through centrifuging to obtain sediment, again
Washed, centrifuged with absolute ethyl alcohol, dried, obtain nano zine oxide.
Advantage of the invention is that
（1）Butyl acrylate, ethyl acrylate, hydroxy-ethyl acrylate, hydroxyethyl methacrylate and itaconic acid, are adsorbed in ZnO
Nanocrystalline nucleating surface, be advantageous to limit its nucleation size and the direction of growth；
（2）The stabilizer of Adipoyl Chloride, oxalyl chloride, chlorobenzoyl chloride, stearic acid chloride, heptadecane acyl chlorides as zinc oxide, while
Butyl acrylate, ethyl acrylate, hydroxy-ethyl acrylate, hydroxyethyl methacrylate and itaconic acid are disperseed；
（3）The compatibility of the materials such as VTES increase butyl acrylate, Adipoyl Chloride and zinc oxide；
（4）Zinc-oxide nano particle diameter 10-18nm prepared by the present invention, specific surface area is big, good dispersion, and chemism is high；
（5）Present invention process is easy, and reaction time is short, and yield is high, is adapted to large-scale production.
（6）2- phosphonobutane -1,2,4- tricarboxylic acids sodium salt, hydroxy ethylene diphosphonic acid add butyl acrylate, propylene
Acetoacetic ester, hydroxy-ethyl acrylate, hydroxyethyl methacrylate and itaconic acid, Adipoyl Chloride, oxalyl chloride, chlorobenzoyl chloride, stearoylketene
Chlorine, heptadecane acyl chlorides are to the dispersion effect of zinc oxide.
Embodiment
Example 1
Weigh zinc sulfate 0.14g to be put into 500mL beakers, add 40g deionized waters, beaker is placed on magnetic stirring apparatus, room
The lower stirring of temperature is to being completely dissolved, then 0.12g ammonium carbonates are added into above-mentioned solution, and stirring at room temperature centrifuges to reacting complete
White depositions Zn5(CO3)2(OH)6；Above-mentioned sediment is poured into 250mL three-necked flasks, takes 5g Adipoyl Chlorides, the second of vinyl three
TMOS 2g, butyl acrylate 3g and 2- phosphonobutane -1,2,4- tricarboxylic acids sodium salts 0.2g addition there-necked flasks, magnetic agitation,
Vacuumize, mixed liquor is to 120 DEG C in electric jacket heating there-necked flask, and is incubated 60min；It is fast under magnetic agitation and nitrogen protection
Speed heating mixed solution is incubated 60min to 300 DEG C, then naturally cools to room temperature, is added into obtained mixture anhydrous
Ethanol 50mL, through centrifuging to obtain sediment, washed, centrifuged with absolute ethyl alcohol 60mL again, dried, obtain nano zine oxide.
Example 2
Weigh zinc sulfate 0.24g to be put into beaker, add 60g deionized waters, beaker is placed on magnetic stirring apparatus, at room temperature
Stirring is to being completely dissolved, then 0.20g potassium carbonate is added into above-mentioned solution, and magnetic agitation centrifuges to reacting complete at room temperature
White depositions Zn5(CO3)2(OH)6；Above-mentioned sediment is poured into three-necked flask, takes 2g oxalyl chlorides, vinyl triethoxyl silicon
Alkane 2g, ethyl acrylate 8g and hydroxy ethylene diphosphonic acid 0.3g add there-necked flask, magnetic agitation, vacuumize, utilize electric jacket
Mixed liquor is to 160 DEG C in heating there-necked flask, and is incubated 30min；Under magnetic agitation and nitrogen protection, mixed solution is heated rapidly
To 280 DEG C, and be incubated 90min, then naturally cool to room temperature, into obtained mixture add absolute ethyl alcohol 80mL, through from
Gains in depth of comprehension sediment, washed, centrifuged with absolute ethyl alcohol 50ml again, dried, obtain nano zine oxide.
Example 3
Weigh zinc sulfate 0.34g to be put into beaker, add 60g deionized waters, beaker is placed on magnetic stirring apparatus, at room temperature
Stirring is to being completely dissolved, then 0.20g potassium carbonate is added into above-mentioned solution, and magnetic agitation centrifuges to reacting complete at room temperature
White depositions Zn5(CO3)2(OH)6；Above-mentioned sediment is poured into three-necked flask, measures 2g chlorobenzoyl chlorides, the ethoxy of vinyl three
Base silane 2g, hydroxy-ethyl acrylate 8g add there-necked flask, magnetic agitation, vacuumize, and are heated in there-necked flask and mixed using electric jacket
Liquid is incubated 30min to 160 DEG C；Under magnetic agitation and nitrogen protection, the rapid mixed solution that heats is incubated to 280 DEG C
90min, room temperature is then naturally cooled to, absolute ethyl alcohol 60ml is added into obtained mixture, through centrifuging to obtain sediment, again
Washed, centrifuged with absolute ethyl alcohol 70ml, dried, obtain nano zine oxide.
Example 4
Weigh zinc sulfate 0.42g to be put into beaker, add 70g deionized waters, beaker is placed on magnetic stirring apparatus, at room temperature
Stirring is to being completely dissolved, then 0.20g potassium carbonate is added into above-mentioned solution, and magnetic agitation centrifuges to reacting complete at room temperature
White depositions；Above-mentioned sediment is poured into three-necked flask, takes 2g stearic acid chlorides, VTES 2g, methyl-prop
Olefin(e) acid hydroxyl ethyl ester 8g adds there-necked flask, magnetic agitation, vacuumizes, using mixed liquor in electric jacket heating there-necked flask to 160 DEG C, and
It is incubated 30min；Under magnetic agitation and nitrogen protection, the rapid mixed solution that heats is incubated 90min to 280 DEG C, then natural
Room temperature is cooled to, absolute ethyl alcohol 50ml is added into obtained mixture, through centrifuging to obtain sediment, is washed again with absolute ethyl alcohol
50ml, centrifuge, dry, obtain nano zine oxide.
Example 5
Weigh zinc sulfate 0.26g to be put into beaker, add 80g deionized waters, beaker is placed on magnetic stirring apparatus, at room temperature
Stirring is to being completely dissolved, then 0.20g potassium carbonate is added into above-mentioned solution, and magnetic agitation centrifuges to reacting complete at room temperature
White depositions；Above-mentioned sediment is poured into three-necked flask, measures 2g heptadecanes acyl chlorides, VTES 2g and clothing
Health acid 8g adds there-necked flask, magnetic agitation, vacuumizes, and using mixed liquor in electric jacket heating there-necked flask to 160 DEG C, and is incubated
30min；Under magnetic agitation and nitrogen protection, the rapid mixed solution that heats is incubated 90min to 280 DEG C, then natural cooling
To room temperature, absolute ethyl alcohol 50ml is added into obtained mixture, through centrifuging to obtain sediment, is washed again with absolute ethyl alcohol
50ml, centrifuge, dry, obtain nano zine oxide.
Gained nano zine oxide is detected, found
The technical indicator of the nano zine oxide of table 1
The average grain diameter of the nano zine oxide prepared by the present invention is smaller than the Particle Size of Nanometer ZnO in market as can be found from Table 1,
It is bigger than surface, and its density is higher than the nano zine oxide in market.
Claims (8)
1. a kind of nano zine oxide, it is characterised in that the preparation method of the nano zine oxide is specially：
Weigh zinc sulfate to be put into beaker, add deionized water, beaker is placed on magnetic stirring apparatus, stirred at room temperature to complete
Dissolving, then ammonium carbonate is added into above-mentioned solution, stirring at room temperature centrifuges to obtain white depositions Zn to reacting complete5(CO3)2
(OH)6；Above-mentioned sediment is poured into three-necked flask, takes Adipoyl Chloride, VTES, butyl acrylate and 2- phosphines
Sour butane -1,2,4- tricarboxylic acids sodium salt add there-necked flask, magnetic agitation, vacuumize, electric jacket heating there-necked flask in mixed liquor extremely
120 DEG C, and it is incubated 60min；Under magnetic agitation and nitrogen protection, the rapid mixed solution that heats is incubated 60min to 300 DEG C,
Then room temperature is naturally cooled to, absolute ethyl alcohol 50mL is added into obtained mixture, through centrifuging to obtain sediment, again with anhydrous
Ethanol 60mL is washed, and is centrifuged, and is dried, is obtained nano zine oxide raw material.
2. nano zine oxide as claimed in claim 1, it is characterised in that：The Adipoyl Chloride can use oxalyl chloride, benzoyl
Chlorine, stearic acid chloride, heptadecane acyl chlorides are replaced.
3. nano zine oxide as claimed in claim 1 or 2, it is characterised in that：The butyl acrylate can use acrylic acid second
Ester, hydroxy-ethyl acrylate, hydroxyethyl methacrylate, itaconic acid are replaced.
4. nano zine oxide as claimed in claim 1 or 2, it is characterised in that：The ammonium carbonate can use potassium carbonate to replace.
5. nano zine oxide as claimed in claim 1 or 2, it is characterised in that：2- phosphonobutanes -1,2,4- tricarboxylic acids the sodium salts
Hydroxy ethylene diphosphonic acid can be used to replace.
6. nano zine oxide as claimed in claim 1 or 2, it is characterised in that：The average grain diameter of the nano zine oxide be 10nm,
15nm, 16nm, 18nm or 20nm.
7. nano zine oxide as claimed in claim 6, it is characterised in that：The specific surface area of the nano zine oxide is 76 m2/g 、
86 m2/g、87m2/g、89m2/g、98m2/g。
8. nano zine oxide as claimed in claim 6, it is characterised in that：The real density of the nano zine oxide is 7.6g/cm3、
8.6g/cm3、8.9g/cm3、9.8 g/cm3。
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| CN112194170A (en) * | 2020-11-19 | 2021-01-08 | 安徽锦华氧化锌有限公司 | Preparation method of modified nano zinc oxide |
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| CN111420652B (en) * | 2020-04-22 | 2023-07-18 | 安徽锦华氧化锌有限公司 | Application of active zinc oxide in promotion of azo dye wastewater degradation |
| CN112110475B (en) * | 2020-09-24 | 2022-06-21 | 安徽省含山县锦华氧化锌厂 | Production process for preparing zinc oxide by using paste precursor |
| CN113716600A (en) * | 2021-09-24 | 2021-11-30 | 石家庄志亿锌业有限公司 | Preparation method of nano zinc oxide |
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| CN1323948C (en) * | 2005-02-02 | 2007-07-04 | 苏州大学 | Preparation method of nanometer zinc oxide |
| CN100554162C (en) * | 2007-09-16 | 2009-10-28 | 中国日用化学工业研究院 | A kind of method for preparing high dispersity nano zinc oxide |
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