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547-68-2 Usage

General Description

Zinc oxalate is a white, odorless, crystalline powder composed of zinc and oxalate ions. It is commonly used in the production of zinc salts, catalysts, and as a precursor for the synthesis of other zinc compounds. Zinc oxalate is insoluble in water but soluble in acids, and it is typically prepared by reacting zinc chloride or zinc nitrate with oxalic acid. It is used in industries such as pharmaceuticals, textiles, and ceramics as a source of zinc for various applications including pigments, catalysts, and corrosion inhibitors. However, it is important to handle zinc oxalate with care as it is considered to be toxic and a potential irritant to the respiratory system if inhaled.

Check Digit Verification of cas no

The CAS Registry Mumber 547-68-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,4 and 7 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 547-68:
(5*5)+(4*4)+(3*7)+(2*6)+(1*8)=82
82 % 10 = 2
So 547-68-2 is a valid CAS Registry Number.
InChI:InChI=1/C2H2O4.Zn/c3-1(4)2(5)6;/h(H,3,4)(H,5,6);

547-68-2 Well-known Company Product Price

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  • Aldrich

  • (544957)  Zincoxalatehydrate  ≥99.99% trace metals basis

  • 547-68-2

  • 544957-5G

  • 755.82CNY

  • Detail

547-68-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name Zinc oxalate, ZnC2O4

1.2 Other means of identification

Product number -
Other names ZINC OXALATE,99.

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:547-68-2 SDS

547-68-2Synthetic route

ZnCl2(bis(4-nitrophenyl)acenaphthenequinonediimine)

ZnCl2(bis(4-nitrophenyl)acenaphthenequinonediimine)

potassium oxalate
583-52-8

potassium oxalate

A

bis(4-nitrophenyl)acenaphthenequinonediimine
444798-17-8

bis(4-nitrophenyl)acenaphthenequinonediimine

B

zinc(II) oxalate
547-68-2

zinc(II) oxalate

Conditions
ConditionsYield
In dichloromethane; water Zn complex was suspended in CH2Cl2 and soln. potassium oxalate in water was added, shaked for 5 min;A 85%
B n/a
[ZnCl2(bis(3,5-dichlorophenyl)acenaphthenequinonediimine)]
845834-87-9

[ZnCl2(bis(3,5-dichlorophenyl)acenaphthenequinonediimine)]

potassium oxalate
583-52-8

potassium oxalate

A

bis(3,5-dichlorophenyl)acenaphthenequinonediimine
357981-03-4

bis(3,5-dichlorophenyl)acenaphthenequinonediimine

B

zinc(II) oxalate
547-68-2

zinc(II) oxalate

Conditions
ConditionsYield
In dichloromethane; water Zn complex was suspended in CH2Cl2 and soln. potassium oxalate in water was added, shaked for 5 min;A 85%
B n/a
ZnCl2(bis(3-trifluoromethylphenyl)acenaphthenequinonediimine)

ZnCl2(bis(3-trifluoromethylphenyl)acenaphthenequinonediimine)

potassium oxalate
583-52-8

potassium oxalate

A

bis(3-trifluoromethylphenyl)acenaphthenequinonediimine
444798-19-0

bis(3-trifluoromethylphenyl)acenaphthenequinonediimine

B

zinc(II) oxalate
547-68-2

zinc(II) oxalate

Conditions
ConditionsYield
In dichloromethane; water Zn complex was suspended in CH2Cl2 and soln. potassium oxalate in water was added, shaked for 5 min;A 85%
B n/a
ZnCl2(bis(4-trifluoromethylphenyl)acenaphthenequinonediimine)

ZnCl2(bis(4-trifluoromethylphenyl)acenaphthenequinonediimine)

potassium oxalate
583-52-8

potassium oxalate

A

bis(4-trifluoromethylphenyl)acenaphthenequinonediimine
226071-20-1

bis(4-trifluoromethylphenyl)acenaphthenequinonediimine

B

zinc(II) oxalate
547-68-2

zinc(II) oxalate

Conditions
ConditionsYield
In dichloromethane; water Zn complex was suspended in CH2Cl2 and soln. potassium oxalate in water was added, shaked for 5 min;A 73%
B n/a
ZnCl2(bis(4-cyanophenyl)acenaphthenequinonediimine)

ZnCl2(bis(4-cyanophenyl)acenaphthenequinonediimine)

potassium oxalate
583-52-8

potassium oxalate

A

bis(4-cyanophenyl)acenaphthenequinonediimine*H2O

bis(4-cyanophenyl)acenaphthenequinonediimine*H2O

B

zinc(II) oxalate
547-68-2

zinc(II) oxalate

Conditions
ConditionsYield
In dichloromethane; water Zn complex was suspended in CH2Cl2 and soln. potassium oxalate in water was added, shaked for 5 min;A 70%
B n/a
ZnCl2(bis(3,5-dinitrophenyl)acenaphthenequinonediimine)

ZnCl2(bis(3,5-dinitrophenyl)acenaphthenequinonediimine)

potassium oxalate
583-52-8

potassium oxalate

A

bis(3,5-dinitrophenyl)acenaphthenequinonediimine*2H2O

bis(3,5-dinitrophenyl)acenaphthenequinonediimine*2H2O

B

zinc(II) oxalate
547-68-2

zinc(II) oxalate

Conditions
ConditionsYield
In dichloromethane; water Zn complex was suspended in CH2Cl2 and soln. potassium oxalate in water was added, shaked for 5 min;A 70%
B n/a
[ZnCl2(bis(3,5-bis(trifluoromethyl)phenyl)acenaphthenequinonediimine)]
798567-18-7

[ZnCl2(bis(3,5-bis(trifluoromethyl)phenyl)acenaphthenequinonediimine)]

potassium oxalate
583-52-8

potassium oxalate

A

N,N'-bis(bis(3,5-trifluoromethyl)phenyl)acenaphthenequinonediimine
226071-21-2

N,N'-bis(bis(3,5-trifluoromethyl)phenyl)acenaphthenequinonediimine

B

zinc(II) oxalate
547-68-2

zinc(II) oxalate

Conditions
ConditionsYield
In dichloromethane; water Zn complex was suspended in CH2Cl2 and soln. potassium oxalate in water was added, shaked for 5 min;A 65%
B n/a
[Zn(II)(2,4'-bipyridine)(oxalato)]

[Zn(II)(2,4'-bipyridine)(oxalato)]

A

zinc(II) oxalate
547-68-2

zinc(II) oxalate

B

zinc(II) oxide

zinc(II) oxide

Conditions
ConditionsYield
In solid heating in air at 270-340°C; elem. anal.;A n/a
B 6%
[Zn(II)(2,2'-bipyridine)(oxalato)]
278175-81-8

[Zn(II)(2,2'-bipyridine)(oxalato)]

A

zinc(II) oxalate
547-68-2

zinc(II) oxalate

B

zinc(II) oxide

zinc(II) oxide

Conditions
ConditionsYield
In solid heating in air at 310-410°C; elem. anal.;A 2%
B n/a
oxalic acid
144-62-7

oxalic acid

zinc(II) oxalate
547-68-2

zinc(II) oxalate

Conditions
ConditionsYield
With acetone; zinc(II) chloride
ZnC2O4+2 H2O

ZnC2O4+2 H2O

zinc(II) oxalate
547-68-2

zinc(II) oxalate

Conditions
ConditionsYield
at 240℃;
at 115℃; under 10 Torr;
oxalic acid
144-62-7

oxalic acid

zinc(II) carbonate
743369-26-8

zinc(II) carbonate

zinc(II) oxalate
547-68-2

zinc(II) oxalate

Conditions
ConditionsYield
In water zinc carbonate added with stirring to soln. of oxalic acid at 60 °C, stirred for 2 h; ppt. filtered, washed with water, dried at 100 °C; elem. anal.;
oxalic acid dihydrate
6153-56-6

oxalic acid dihydrate

zinc(II) acetate dihydrate
5970-45-6

zinc(II) acetate dihydrate

zinc(II) oxalate
547-68-2

zinc(II) oxalate

Conditions
ConditionsYield
With nonyl phenyl ether In neat (no solvent) stoich. amt. of reactants mixed with ether in mortar; ground for severalmin and kept in thermostate oven at 50-60 °C for 6 h; washed several times with distilled water and acetone; dried in oven at 70-80 °C for 12 h;
In water at 5℃; for 2h;
zinc oxalate * 2 methanol

zinc oxalate * 2 methanol

zinc(II) oxalate
547-68-2

zinc(II) oxalate

Conditions
ConditionsYield
byproducts: CH3OH; at 60°C;;
2 zinc oxalate * potassium oxalate * potassium thiocyanate * 6 water

2 zinc oxalate * potassium oxalate * potassium thiocyanate * 6 water

zinc(II) oxalate
547-68-2

zinc(II) oxalate

Conditions
ConditionsYield
In water on pouring over with H2O, pptg. of Zn oxalate;;
In water on pouring over with H2O, pptg. of Zn oxalate;;
zinc(II) formate
557-41-5

zinc(II) formate

zinc(II) oxalate
547-68-2

zinc(II) oxalate

Conditions
ConditionsYield
sodium amide at temp. below melting point of amid, violent react.;;
sodium amide on heating at 200°C;;
sodium amide at temp. below melting point of amid, violent react.;;
sodium amide on heating at 200°C;;
zinc oxalate * 2 potassium formate

zinc oxalate * 2 potassium formate

zinc(II) oxalate
547-68-2

zinc(II) oxalate

Conditions
ConditionsYield
In water on shaking with H2O, dissolving and pptg. of Zn oxalate;;
In water on shaking with H2O, dissolving and pptg. of Zn oxalate;;
zinc oxalate dihydrate
16788-40-2, 85655-72-7

zinc oxalate dihydrate

zinc(II) oxalate
547-68-2

zinc(II) oxalate

Conditions
ConditionsYield
In neat (no solvent) byproducts: H2O; heating (quasi-isothermal conditions, 428 K); TGA;
In neat (no solvent) Kinetics; byproducts: H2O; investigation of kinetics and mechanism of the dehydration;
Kinetics; thermal decompn. under N2 between 105 and 135°C;
In neat (no solvent, solid phase) byproducts: H2O; dehydrated in a N2 stream in a tube furnace;
In neat (no solvent, solid phase) thermal decompn. of ZnC2O4*2H2O (air); depending on stoichiometry of educt two different crystalforms obtained;
sodium oxalate
62-76-0

sodium oxalate

zinc(II) sulfate
7733-02-0

zinc(II) sulfate

zinc(II) oxalate
547-68-2

zinc(II) oxalate

Conditions
ConditionsYield
In not given
zinc(II) nitrate
10196-18-6

zinc(II) nitrate

oxalic acid
144-62-7

oxalic acid

sodium di-2-ethylhexyl sulfosuccinate
34098-39-0

sodium di-2-ethylhexyl sulfosuccinate

zinc(II) oxalate
547-68-2

zinc(II) oxalate

Conditions
ConditionsYield
In diethyl ether; ethanol byproducts: NaNO3; pptn. on mixing Zn-salt soln. (dry EtOH) with Na-salt soln. (dry ether),NaNO3 ppt. filtration off, filtrate washing (dry benzene), dissoln. in isooctane, dry EtOH addn., powder oxalic acid addn., mixt. stirring for 1 h; ppt. sepn. (centrifugation), washing (MeOH/CHCl3 1:1, acetone/MeOH 1:1),drying;
zinc(II) nitrate
10196-18-6

zinc(II) nitrate

calcium(II) oxalate
781577-54-6

calcium(II) oxalate

zinc(II) oxalate
547-68-2

zinc(II) oxalate

Conditions
ConditionsYield
In not given concd. Zn(NO3)2 soln.;;
In not given concd. Zn(NO3)2 soln.;;
calcium(II) oxalate
781577-54-6

calcium(II) oxalate

zinc(II) chloride
7646-85-7

zinc(II) chloride

zinc(II) oxalate
547-68-2

zinc(II) oxalate

Conditions
ConditionsYield
In not given concd. ZnCl2 soln.;;
In not given concd. ZnCl2 soln.;;
zinc(II) sulfate hydrate

zinc(II) sulfate hydrate

oxalic acid
144-62-7

oxalic acid

zinc(II) oxalate
547-68-2

zinc(II) oxalate

Conditions
ConditionsYield
In water addn. of soln. of M(II)SO4 to soln. of oxalic acid;
zinc(II) chloride dihydrate

zinc(II) chloride dihydrate

oxalic acid
144-62-7

oxalic acid

zinc(II) oxalate
547-68-2

zinc(II) oxalate

Conditions
ConditionsYield
In water hot oxalic acid soln. was added to aq. soln. of Zn salt;
oxalic acid
144-62-7

oxalic acid

zinc(II) chloride
7646-85-7

zinc(II) chloride

zinc(II) oxalate
547-68-2

zinc(II) oxalate

Conditions
ConditionsYield
In acetone on addn. (drop by drop) of ZnCl2 in acetone to soln. of oxalic acid/acetone with complete exclusion of water;;
In water for 2h;
ammonium oxalate

ammonium oxalate

zinc(II) chloride
7646-85-7

zinc(II) chloride

zinc(II) oxalate
547-68-2

zinc(II) oxalate

Conditions
ConditionsYield
In water compd. is still containing 0.79% H2O after drying at 240°C;;
zinc(II) nitrate hexahydrate

zinc(II) nitrate hexahydrate

oxalic acid dihydrate
6153-56-6

oxalic acid dihydrate

zinc(II) oxalate
547-68-2

zinc(II) oxalate

Conditions
ConditionsYield
In water water removed under vac. at 353 K;
Stage #1: zinc(II) nitrate hexahydrate With HoVO4 for 0.5h;
Stage #2: oxalic acid dihydrate In water for 4h;
With tetraethylammonium hydroxide; sodium hydroxide In water pH=10;
{CH3NH3}2Zn(oxalate)2 * (monomethylamine)

{CH3NH3}2Zn(oxalate)2 * (monomethylamine)

zinc(II) oxalate
547-68-2

zinc(II) oxalate

Conditions
ConditionsYield
In neat (no solvent) byproducts: monomethylamine, CO, CO2; thermal decompn. (225-374°C, air, heating rate 5°C/min):; differential thermal anal., thermogravimetry;;
ammonium oxalate

ammonium oxalate

zinc(II) carbonate
743369-26-8

zinc(II) carbonate

A

Zn(2+)*4NH4(1+)*3C2O4(2-)*3H2O=Zn(NH4)4(C2O4)3*3H2O

Zn(2+)*4NH4(1+)*3C2O4(2-)*3H2O=Zn(NH4)4(C2O4)3*3H2O

B

zinc(II) oxalate
547-68-2

zinc(II) oxalate

Conditions
ConditionsYield
In not given saturating a soln. of (NH4)2C2O4 with ZnCO3 at digestion for a longer period of time; evaporation;; first pptn. of ZnC2O4; pptn.;;
zinc(II) oxalate
547-68-2

zinc(II) oxalate

sodium carbonate
497-19-8

sodium carbonate

zinc(II) carbonate
743369-26-8

zinc(II) carbonate

Conditions
ConditionsYield
In not given on react. of soln. of zinc oxalate with 3n Na2CO3;;99%
In water99%
In not given on react. of soln. of zinc oxalate with 3n Na2CO3;;99%
In water99%
zinc(II) oxalate
547-68-2

zinc(II) oxalate

2-(2-Aminoethylamino)ethanol
111-41-1

2-(2-Aminoethylamino)ethanol

(oxalato bis-(hydroxyethyl)ethylenediamine) zinc(II)
79949-88-5

(oxalato bis-(hydroxyethyl)ethylenediamine) zinc(II)

Conditions
ConditionsYield
two-fold excess of the N-(2-hydroxyethyl)ethylendiamine was added to the Zn oxalate, triturated and allowed to stand for 1 h; ppt. was filtered off, washed with ethanol and then with ether and dried in a vac. desiccator; chem. anal.;90%
ferric oxalate
15843-42-2

ferric oxalate

zinc(II) oxalate
547-68-2

zinc(II) oxalate

zinc ferrite

zinc ferrite

Conditions
ConditionsYield
In water at 135℃; for 24h; Time; Autoclave;84%
piperazine
110-85-0

piperazine

zinc(II) oxalate
547-68-2

zinc(II) oxalate

sodium hydrogensulfite

sodium hydrogensulfite

[1,4-diazabicyclo[2.2.2]octane]0.5[Zn2(sulfite)2(oxalate)0.5(H2O)2]

[1,4-diazabicyclo[2.2.2]octane]0.5[Zn2(sulfite)2(oxalate)0.5(H2O)2]

Conditions
ConditionsYield
In water at 115℃; for 120h; pH=6;72%
zinc(II) oxalate
547-68-2

zinc(II) oxalate

ZnO

ZnO

Conditions
ConditionsYield
at 405℃;
at 405℃;
zinc(II) oxalate
547-68-2

zinc(II) oxalate

zinc(II) oxide

zinc(II) oxide

Conditions
ConditionsYield
In neat (no solvent) decompn. temp. should be at least 400°C;;
air; heating (418 K, 0.5 h), heating (5 K/min, to 653 K), calcination (673 K, 4 h);
decompn.;;
strontium(II) carbonate
1633-05-2

strontium(II) carbonate

nickel(II) oxalate
547-67-1

nickel(II) oxalate

lanthanum oxalate

lanthanum oxalate

zinc(II) oxalate
547-68-2

zinc(II) oxalate

La1.9Sr0.1Ni0.9Zn0.1O(4+x)

La1.9Sr0.1Ni0.9Zn0.1O(4+x)

Conditions
ConditionsYield
In neat (no solvent) heating at 1470K for 48h in air wih one intermediate grinding, annealed at 1420K for 24h in air;
zinc(II) oxalate
547-68-2

zinc(II) oxalate

ethylenediamine
107-15-3

ethylenediamine

zinc oxalate * 3 ethylene diamine

zinc oxalate * 3 ethylene diamine

lanthanum(III) oxide

lanthanum(III) oxide

zinc(II) oxalate
547-68-2

zinc(II) oxalate

barium carbonate

barium carbonate

La2BaZnO5

La2BaZnO5

Conditions
ConditionsYield
In neat (no solvent) pressing (ratio of educts 1:1:1), heating (1100°C, >20 days, powder diffraction monitoring), melting (CO2-laser, 30 min), slow cooling to 600°C;
potassium hypophosphite
7782-87-8

potassium hypophosphite

water
7732-18-5

water

zinc(II) oxalate
547-68-2

zinc(II) oxalate

2 zinc oxalate * 3 potassium hypophosphite * 2 water

2 zinc oxalate * 3 potassium hypophosphite * 2 water

Conditions
ConditionsYield
In water on satg. of aq. K hypophosphite with ZnC2O4 and heating at boiling point;;
In water on satg. of aq. K hypophosphite with ZnC2O4 and heating at boiling point;;
water
7732-18-5

water

potassium oxalate
583-52-8

potassium oxalate

zinc(II) oxalate
547-68-2

zinc(II) oxalate

2K(1+)*Zn(2+)*2C2O4(2-)*6H2O=K2Zn(C2O4)2*6H2O

2K(1+)*Zn(2+)*2C2O4(2-)*6H2O=K2Zn(C2O4)2*6H2O

Conditions
ConditionsYield
In not given on heating of soln., satd. with K oxalate at 25°C, up to boiling, addn. of Zn oxalate in small excess, filtration , cooling down at 40°C; storing of mother liquor on air at 20 - 25°C for 3 - 4 days;;
potassium nitrite
7758-09-0

potassium nitrite

water
7732-18-5

water

zinc(II) oxalate
547-68-2

zinc(II) oxalate

2 zinc oxalate * potassium oxalate * potassium nitrite * 6 water

2 zinc oxalate * potassium oxalate * potassium nitrite * 6 water

Conditions
ConditionsYield
In acetic acid on addn. of Zn oxalate to hot soln. of KNO2, neutralized with acetic acid;;
In acetic acid aq. acetic acid; on addn. of Zn oxalate to hot soln. of KNO2, neutralized with acetic acid;;
water
7732-18-5

water

zinc(II) oxalate
547-68-2

zinc(II) oxalate

ethylamine
75-04-7

ethylamine

zinc oxalate * ethylamine * water

zinc oxalate * ethylamine * water

Conditions
ConditionsYield
In water on satg. of aq. ethylamine with anhyd. ZnC2O4 and concg. to dryness or on addn. of 96% alc. (ninefold excess) to Zn oxalate ethylamine mixture and filtration of ppt.;;
nickel(II) oxalate
547-67-1

nickel(II) oxalate

zinc(II) oxalate
547-68-2

zinc(II) oxalate

ferric nitrate
7782-61-8

ferric nitrate

zinc nickel ferrite

zinc nickel ferrite

Conditions
ConditionsYield
With citric acid In water 3 M citric soln mixed with each metal solns.; heated at 40°C for .apprx.30 min; viscous gel obtained after slow evapn.; heated at .apprx.200°C; ignited; calcined at 1000°C; detd.by XRD;
With citric acid In water stoich.; citric acid soln. added to metal soln., heated at 40°C for approx. 30 min with continuous stirring, slowly evapd. until highly viscous gel was formed, heated at .apprx. 200°C (ignition), residue calcined at 1000°C for 2 h;

547-68-2Relevant articles and documents

Non-isothermal studies for the decomposition course of CdC 2O4-ZnC2O4 mixture in air

Gabal

, p. 55 - 62 (2004)

The thermal decomposition of cadmium-zinc oxalate (1:1mol ratios) mixture in air was investigated by non-isothermal thermogravimetric analysis. Intermediates and the final products were characterized by X-ray diffraction and scanning electron microscopy techniques. TG showed that the mixture dehydrated in two steps and decomposed exothermically to CdO-ZnO mixture at 390°C in a further two steps. The observed increase in the intensity of the X-ray diffraction lines by raising the calcination temperature from 400 to 800°C is attributed to the grain growth of CdO-ZnO mixture as revealed from SEM experiments. The kinetics of the oxalate decomposition steps was performed using the various reaction interface models and differential techniques of computational analysis of non-isothermal data. The activation parameters, calculated using the integral composite method, showed that the reactions were best described by the random nucleation model characteristic of solid state nucleation growth mechanism. The results of activation parameters for the different decomposition steps are compared and discussed.

Synthesis, crystal structure, and properties of two zinc(II) complexes with 2-propyl-4,5-imidazoledicarboxylic acid

Luo, Zhirong,Zhuang, Jichang,Wu, Qiaolan,Yin, Xianhong,Zheng, Xiaoxia,Wei, Huan

, p. 455 - 462 (2012)

A tetradentate 2-propyl-4,5-imidazoledicarboxylic acid [H3pimdc] reacts with zinc sulfate in the ethanol aqueous solution and zinc acetate in the N,N-dimethylformamide (DMF) aqueous solution to give two complexes [Zn(H 2pimdc)2(H2O)2]·4H 2O and [Zn(H2pimdc)2(H2O) 2]·2DMF. The complexes were characterized by X-ray single crystal analysis, thermal analysis, and IR spectrum. Because of the different coordination of water, complex 1 forms a fishing net-like latticed topology geometry via hydrogen bonds and π-π stacking interaction, but complex 2 forms a layer-like topology geometry via hydrogen bonds and π-π stacking interaction. Copyright Taylor & Francis Group, LLC.

Solar photocatalytic and self-cleaning performances of HoVO4 doped ZnO

Thirumalai, Kuppulingam,Shanthi, Manohar,Swaminathan, Meenakshisundaram

, p. 178 - 187 (2018)

In this article we report preparation of 5 wt% HoVO4 doped ZnO via template-free hydrothermal process and investigated its photocatalytic activity against azo dyes Rhodamine-B (Rh-B), Trypan Blue (TB) and Acid Black 1 (AB 1) in solar light irradiation. Th

Synthesis of ZnO nanoparticles for varistor application using Zn-substituted aerosol OT microemulsion

Singhal,Chhabra,Kang,Shah

, p. 239 - 247 (1997)

This paper describes a new method for the synthesis of zinc oxide nanoparticles using ethanol-in-oil microemulsions with Zn-DEHSS (diethylhexyl sulfosuccinate) as surfactant. The zinc oxide nanoparticles find application in varistors and other functional devices. These particles have been characterized by X-ray diffraction, TEM, and BET surface area. Microemulsion droplets were characterized by quasi elastic light scattering (QELS). Varistors formed from doped zinc oxide nanoparticles finds application as low voltage surge devices with low leakage current and high coefficient of nonlinearity (α). In this paper, we have shown that the critical voltage of the varistor is related to the grain size which is related to size of ZnO particles. The smaller ZnO particles lead to larger grain size, thereby lowering the critical voltage.

Huettig,Klappholz

, p. 225,228 (1932)

Giovanoli,Wiedemann

, p. 1134,1135,1138,1139,1148 (1968)

Defect-enhanced photocatalytic activity of ZnO micro/nanostructures

Wang, Yu,Yan, Mei,Chen, Qinguo,Peng, Yin

, p. 1557 - 1563 (2013)

ZnO micro/nanocrystals with controlled oxygen defects are successfully prepared through annealing precursors obtained via a simple solvothermal method. The size and surface defects of the as-synthesized ZnO micro/nanocrystals increase with the solvent volume ratio of water/ethanol increasing; the BET surface areas of the corresponding samples decrease during these processes; photoluminescence reveals that the type and concentration of surface defects (oxygen vacancy and interstitial oxygen) are quite different for the samples prepared via different solvent volume ratio of water/ethanol. In addition, it is found that the photocatalytic activity of the synthesized ZnO nanocrystals is mainly dependent on the concentration of surface defects. The sample with more surface defects exhibits higher photocatalytic activity toward the degradation of methylene blue (MB). The possible photocatalytic mechanism is discussed in detail. Copyright

Photocatalytic oxidation of methane over CuO-decorated ZnO nanocatalysts

Li, Zhonghua,Pan, Xiaoyang,Yi, Zhiguo

, p. 469 - 475 (2019/01/09)

Catalytic oxidation of methane under mild conditions remains a challenge in the industrial catalytic processes. Herein, we report a highly efficient CuO/ZnO nanocomposite photocatalyst for methane oxidation under ambient conditions. It was found that both the CH4 photooxidative activity and stability over ZnO are considerably improved by loading a tiny amount of CuO, though CuO itself exhibits no activity on methane oxidation. On the basis of the experimental results in conjunction with in situ electron paramagnetic resonance (EPR) and Fourier transform infrared spectroscopy (FTIR) studies, the photocatalytic reaction process of CH4 over CuO/ZnO composite microstructures is comprehensively discussed.

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