The synthesis of gold nanoparticles by a citrate-radiolytical method
- 1. Division of Materials Chemistry, Ruđer Bošković Institute, Bijenička 54, HR-10002 Zagreb (Croatia)
- 2. Division of Materials Physics, Ruđer Bošković Institute, Bijenička 54, HR-10002 Zagreb (Croatia)
Description
The classical citrate method is based on the reduction of an Au(III) precursor with sodium citrate in an aqueous solution near the boiling point. In this work gold nanoparticles (GNPs) were synthesised via a citrate method using reduction by gamma-irradiation at room temperature. The Au(III)–citrate aqueous precursor solution was gamma-irradiated to doses of up to 30 kGy. The dose rate of gamma-irradiation was ∼8 kGy h−1. The GNP size was controlled by the adsorbed dose as well as by different saturated gases (air or nitrogen) present in precursor solutions. The results showed that gamma-irradiation produced smaller GNPs in the presence of precursor solutions saturated with nitrogen compared with the ones saturated with air. By increasing both the gold(III) and citrate concentrations in precursor solutions, stable and highly concentrated colloidal gold/citrate suspensions were synthesised using classical and citrate-radiolytical reduction methods. Gamma-irradiation thus produced well-dispersed and highly concentrated GNPs in an aqueous citrate solution in the presence of dissolved oxygen and without adding any reducing or stabilising agents. Radiolytically intensified citrate oxidation and decarboxylation to acetone and other products by dissolved oxygen was advantageous for Au(III) reduction and subsequent formation of gold nanoparticles. Since the completely same precursor solutions were used both in the classical and citrate-radiolytical reduction methods, a real comparison of GNP sizes between these two methods was given. - Highlights: • Gold nanoparticles were synthesised by classical and citrate-radiolytical methods. • The size of gold nanoparticles was controlled by different saturated gases. • Radiolytically intensified citrate oxidation is advantageous for Au(III) reduction. • A comparison of particle sizes between classical and radiolytical methods was made
Availability note (English)
Available from http://dx.doi.org/10.1016/j.radphyschem.2014.07.006Additional details
Identifiers
- DOI
- 10.1016/j.radphyschem.2014.07.006;
- PII
- S0969-806X(14)00294-1;
Publishing Information
- Journal Title
- Radiation Physics and Chemistry (1993)
- Journal Volume
- 106
- Journal Page Range
- p. 77-82
- ISSN
- 0969-806X
- CODEN
- RPCHDM
INIS
- Country of Publication
- United Kingdom
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 46124386
- Subject category
- S38: RADIATION CHEMISTRY, RADIOCHEMISTRY AND NUCLEAR CHEMISTRY;
- Descriptors DEI
- ACETONE; AQUEOUS SOLUTIONS; CITRATES; COMPARATIVE EVALUATIONS; CONCENTRATION RATIO; DECARBOXYLATION; DISSOLVED GASES; DOSE RATES; GAMMA RADIATION; GOLD; IRRADIATION; NANOPARTICLES; OXIDATION; PARTICLE SIZE; RADIATION DOSES; SODIUM COMPOUNDS; SUSPENSIONS; SYNTHESIS; TEMPERATURE RANGE 0273-0400 K
- Descriptors DEC
- ALKALI METAL COMPOUNDS; CARBOXYLIC ACID SALTS; CHEMICAL REACTIONS; DIMENSIONLESS NUMBERS; DISPERSIONS; DOSES; ELECTROMAGNETIC RADIATION; ELEMENTS; EVALUATION; FLUIDS; GASES; HOMOGENEOUS MIXTURES; IONIZING RADIATIONS; KETONES; METALS; MIXTURES; ORGANIC COMPOUNDS; PARTICLES; RADIATIONS; SIZE; SOLUTES; SOLUTIONS; TEMPERATURE RANGE; TRANSITION ELEMENTS
Optional Information
- Copyright
- Copyright (c) 2014 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.