CN106186041A - A kind of method that nano-ZnO is prepared in microwave-assisted pyrolysis - Google Patents

A kind of method that nano-ZnO is prepared in microwave-assisted pyrolysis Download PDF

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Publication number
CN106186041A
CN106186041A CN201610527695.8A CN201610527695A CN106186041A CN 106186041 A CN106186041 A CN 106186041A CN 201610527695 A CN201610527695 A CN 201610527695A CN 106186041 A CN106186041 A CN 106186041A
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CN
China
Prior art keywords
zno
microwave
nano
prepared
completely dissolved
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Pending
Application number
CN201610527695.8A
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Chinese (zh)
Inventor
彭勇刚
纪俊玲
陶永新
汪媛
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Changzhou University
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Changzhou University
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Priority to CN201610527695.8A priority Critical patent/CN106186041A/en
Publication of CN106186041A publication Critical patent/CN106186041A/en
Pending legal-status Critical Current

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    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01GCOMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
    • C01G9/00Compounds of zinc
    • C01G9/02Oxides; Hydroxides
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01PINDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2002/00Crystal-structural characteristics
    • C01P2002/70Crystal-structural characteristics defined by measured X-ray, neutron or electron diffraction data
    • C01P2002/72Crystal-structural characteristics defined by measured X-ray, neutron or electron diffraction data by d-values or two theta-values, e.g. as X-ray diagram
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01PINDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2004/00Particle morphology
    • C01P2004/01Particle morphology depicted by an image
    • C01P2004/04Particle morphology depicted by an image obtained by TEM, STEM, STM or AFM

Abstract

The invention provides a kind of method that nano-ZnO is prepared in microwave-assisted pyrolysis, first 18-amine. is added heat fusing by the method, is subsequently adding zinc nitrate;Nano-ZnO is prepared again by the way of microwave-assisted is pyrolyzed.The method is simple to operate, environmental protection.

Description

A kind of method that nano-ZnO is prepared in microwave-assisted pyrolysis
Technical field
The invention belongs to field of new, be specifically related to a kind of method that nano-ZnO is prepared in microwave-assisted pyrolysis.
Background technology
Nano-ZnO is as a kind of II-VI important race's conductor oxidate, in terms of the photocatalytic degradation of organic pollution Have a wide range of applications.The preparation method of nano-ZnO mainly has: induced with laser CVD, chemical vapor phase oxidation process, chemical precipitation Method, sol-gel process, hydro-thermal method, microemulsion method etc..In these methods, operation is complicated for some, need special equipment;Some Need to use some poisonous and hazardous chemicals.
Summary of the invention
The technical problem to be solved is to provide a kind of method that nano-ZnO is prepared in microwave-assisted pyrolysis, the party Method uses microwave-assisted pyrolysis zinc nitrate, prepares nano-ZnO, simple to operate, environmental protection.
The method that nano-ZnO is prepared in a kind of microwave-assisted pyrolysis that the present invention provides, is carried out as steps described below:
30-100g 18-amine. is heated to 100 DEG C, after it is completely dissolved, adds 0.2-1.0g Zn (NO3)2·6H2O, Being stirred continuously, after solute is completely dissolved, place reaction liquid in microwave reactor, microwave heating, to 180-220 DEG C, is incubated 30-60min, after insulation terminates, collects precipitate, and precipitate uses dehydrated alcohol, distilled water wash 3-5 time respectively, 60-80 DEG C of baking Dry, obtain nano-ZnO.
The invention has the beneficial effects as follows: prepare nano-ZnO by being directly pyrolyzed zinc nitrate in 18-amine. solution, operation Simply, environmental protection.
Accompanying drawing explanation
The XRD figure of Fig. 1 embodiment 1 resulting materials
The TEM figure of Fig. 2 embodiment 1 resulting materials
Detailed description of the invention
Below in conjunction with specific embodiment, the present invention is described in further detail.Should be understood that these embodiments are intended merely to Illustrate the present invention, rather than limit the scope of the present invention by any way.
Embodiment 1
30g 18-amine. is heated to 100 DEG C, after it is completely dissolved, adds 0.2g Zn (NO3)2·6H2O, is stirred continuously, After solute is completely dissolved, place reaction liquid in microwave reactor, microwave heating to 180 DEG C, it is incubated 60min, insulation terminates After, collect precipitate, precipitate uses dehydrated alcohol, distilled water wash 3 times respectively, and 60 DEG C of drying obtain nano-ZnO.
Embodiment 2
100g 18-amine. is heated to 100 DEG C, after it is completely dissolved, adds 1.0g Zn (NO3)2·6H2O, constantly stirs Mix, after solute is completely dissolved, place reaction liquid in microwave reactor, microwave heating to 220 DEG C, it is incubated 30min, insulation knot Shu Hou, collects precipitate, and precipitate uses dehydrated alcohol, distilled water wash 5 times respectively, and 80 DEG C of drying obtain nano-ZnO.
Embodiment 3
60g 18-amine. is heated to 100 DEG C, after it is completely dissolved, adds 0.5g Zn (NO3)2·6H2O, is stirred continuously, After solute is completely dissolved, place reaction liquid in microwave reactor, microwave heating to 200 DEG C, it is incubated 45min, insulation terminates After, collect precipitate, precipitate uses dehydrated alcohol, distilled water wash 4 times respectively, and 70 DEG C of drying obtain nano-ZnO.
Embodiment 4
50g 18-amine. is heated to 100 DEG C, after it is completely dissolved, adds 0.4Zn (NO3)2·6H2O, is stirred continuously, and treats After solute is completely dissolved, place reaction liquid in microwave reactor, microwave heating to 190 DEG C, it is incubated 35min, after insulation terminates, Collecting precipitate, precipitate uses dehydrated alcohol, distilled water wash 5 times respectively, and 75 DEG C of drying obtain nano-ZnO.

Claims (1)

1. the method that nano-ZnO is prepared in a microwave-assisted pyrolysis, it is characterised in that: step is as follows:
30-100g 18-amine. is heated to 100 DEG C, after it is completely dissolved, adds 0.2-1.0g Zn (NO3)2·6H2O, constantly Stirring, after solute is completely dissolved, places reaction liquid in microwave reactor, and microwave heating, to 180-220 DEG C, is incubated 30- 60min, after insulation terminates, collects precipitate, and precipitate uses dehydrated alcohol, distilled water wash 3-5 time respectively, 60-80 DEG C of drying, Obtain nano-ZnO.
CN201610527695.8A 2016-07-06 2016-07-06 A kind of method that nano-ZnO is prepared in microwave-assisted pyrolysis Pending CN106186041A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201610527695.8A CN106186041A (en) 2016-07-06 2016-07-06 A kind of method that nano-ZnO is prepared in microwave-assisted pyrolysis

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201610527695.8A CN106186041A (en) 2016-07-06 2016-07-06 A kind of method that nano-ZnO is prepared in microwave-assisted pyrolysis

Publications (1)

Publication Number Publication Date
CN106186041A true CN106186041A (en) 2016-12-07

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Country Status (1)

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CN (1) CN106186041A (en)

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1657415A (en) * 2005-02-02 2005-08-24 苏州大学 Preparation method of nanometer zinc oxide
CN101274771A (en) * 2007-03-30 2008-10-01 清华大学 Preparation for metallic oxide nanocrystal
CN101717631A (en) * 2009-11-18 2010-06-02 南京邮电大学 Compound of nano zinc oxide and luminous organic matter and preparation method thereof
CN101935875A (en) * 2010-09-14 2011-01-05 浙江大学 Sn-doped ZnO superfine nanowires and synthesis method thereof

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1657415A (en) * 2005-02-02 2005-08-24 苏州大学 Preparation method of nanometer zinc oxide
CN101274771A (en) * 2007-03-30 2008-10-01 清华大学 Preparation for metallic oxide nanocrystal
CN101717631A (en) * 2009-11-18 2010-06-02 南京邮电大学 Compound of nano zinc oxide and luminous organic matter and preparation method thereof
CN101935875A (en) * 2010-09-14 2011-01-05 浙江大学 Sn-doped ZnO superfine nanowires and synthesis method thereof

Non-Patent Citations (4)

* Cited by examiner, † Cited by third party
Title
DING-SHENG WANG ET AL.: "Direct Thermal Decomposition of Metal Nitrates in Octadecylamine to Metal Oxide Nanocrystals", 《CHEM. EUR. J》 *
RIZWAN WAHAB ET AL.: "A non-aqueous synthesis, characterization of zinc oxide nanoparticles and their interaction with DNA", 《SYNTHETIC METALS》 *
叶红勇等: "微波加热制备高分散性纳米氧化锌粉体", 《南阳理工学院学报》 *
李平等: "微波加热制备纳米ZnO 粉体及其表征", 《精细化工》 *

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