Synthesis of Gold Nanoparticles Capped-Benzoic Acid Derivative Compounds (<i>o</i>-, <i>m</i>-, and <i>p</i>-Hydroxybenzoic Acid)
The effect of a hydroxyl functional group of the benzoic acid derivative compound, i.e. o-hydroxybenzoic acid, m-hydroxybenzoic acid, and p-hydroxybenzoic acid on the synthesis of AuNPs has been studied. It was revealed that the pH, heating time, the concentration of capping agent and the concentrat...
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doaj-1bc421edc66e40af811d91a8e7c1fedd2020-11-25T02:46:37ZengUniversitas Gadjah MadaIndonesian Journal of Chemistry1411-94202460-15782019-04-0119237638510.22146/ijc.3444022799Synthesis of Gold Nanoparticles Capped-Benzoic Acid Derivative Compounds (<i>o</i>-, <i>m</i>-, and <i>p</i>-Hydroxybenzoic Acid)Agustina Sus Andreani0Eko Sri Kunarti1Sri Juari Santosa2Department of Chemistry, Faculty of Mathematics and Natural Sciences, Universitas Gadjah Mada, Sekip Utara Yogyakarta 55281, IndonesiaDepartment of Chemistry, Faculty of Mathematics and Natural Sciences, Universitas Gadjah Mada, Sekip Utara Yogyakarta 55281, IndonesiaDepartment of Chemistry, Faculty of Mathematics and Natural Sciences, Universitas Gadjah Mada, Sekip Utara Yogyakarta 55281, IndonesiaThe effect of a hydroxyl functional group of the benzoic acid derivative compound, i.e. o-hydroxybenzoic acid, m-hydroxybenzoic acid, and p-hydroxybenzoic acid on the synthesis of AuNPs has been studied. It was revealed that the pH, heating time, the concentration of capping agent and the concentration of Au3+ affected the formation of AuNPs. We discovered that o-hydroxybenzoic acid possessed the highest stability, yet it needed the highest concentration of Au3+ and faster reaction time than p-hydroxybenzoic acid and slower than m-hydroxybenzoic acid. The stability was verified by means of UV-Vis spectrophotometer, XRD, TEM, Particle Size Analyzer (PSA), and Zeta Potential with an aging time of more than 5 months. We concluded that o-hydroxybenzoic acid acquired the most effective redox reaction instead of m-hydroxybenzoic acid and p-hydroxybenzoic acid, resulted in the smaller sized and unaggregated AuNPs. We also confirmed that the hydroxyl group of o-hydroxybenzoic acid, m-hydroxybenzoic acid and p-hydroxybenzoic acid is the functional group responsible for the reduction of Au3+ to Au0.https://jurnal.ugm.ac.id/ijc/article/view/34440AuNPso-hydroxybenzoic acidm-hydroxybenzoic acidp-hydroxybenzoic acid |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Agustina Sus Andreani Eko Sri Kunarti Sri Juari Santosa |
spellingShingle |
Agustina Sus Andreani Eko Sri Kunarti Sri Juari Santosa Synthesis of Gold Nanoparticles Capped-Benzoic Acid Derivative Compounds (<i>o</i>-, <i>m</i>-, and <i>p</i>-Hydroxybenzoic Acid) Indonesian Journal of Chemistry AuNPs o-hydroxybenzoic acid m-hydroxybenzoic acid p-hydroxybenzoic acid |
author_facet |
Agustina Sus Andreani Eko Sri Kunarti Sri Juari Santosa |
author_sort |
Agustina Sus Andreani |
title |
Synthesis of Gold Nanoparticles Capped-Benzoic Acid Derivative Compounds (<i>o</i>-, <i>m</i>-, and <i>p</i>-Hydroxybenzoic Acid) |
title_short |
Synthesis of Gold Nanoparticles Capped-Benzoic Acid Derivative Compounds (<i>o</i>-, <i>m</i>-, and <i>p</i>-Hydroxybenzoic Acid) |
title_full |
Synthesis of Gold Nanoparticles Capped-Benzoic Acid Derivative Compounds (<i>o</i>-, <i>m</i>-, and <i>p</i>-Hydroxybenzoic Acid) |
title_fullStr |
Synthesis of Gold Nanoparticles Capped-Benzoic Acid Derivative Compounds (<i>o</i>-, <i>m</i>-, and <i>p</i>-Hydroxybenzoic Acid) |
title_full_unstemmed |
Synthesis of Gold Nanoparticles Capped-Benzoic Acid Derivative Compounds (<i>o</i>-, <i>m</i>-, and <i>p</i>-Hydroxybenzoic Acid) |
title_sort |
synthesis of gold nanoparticles capped-benzoic acid derivative compounds (<i>o</i>-, <i>m</i>-, and <i>p</i>-hydroxybenzoic acid) |
publisher |
Universitas Gadjah Mada |
series |
Indonesian Journal of Chemistry |
issn |
1411-9420 2460-1578 |
publishDate |
2019-04-01 |
description |
The effect of a hydroxyl functional group of the benzoic acid derivative compound, i.e. o-hydroxybenzoic acid, m-hydroxybenzoic acid, and p-hydroxybenzoic acid on the synthesis of AuNPs has been studied. It was revealed that the pH, heating time, the concentration of capping agent and the concentration of Au3+ affected the formation of AuNPs. We discovered that o-hydroxybenzoic acid possessed the highest stability, yet it needed the highest concentration of Au3+ and faster reaction time than p-hydroxybenzoic acid and slower than m-hydroxybenzoic acid. The stability was verified by means of UV-Vis spectrophotometer, XRD, TEM, Particle Size Analyzer (PSA), and Zeta Potential with an aging time of more than 5 months. We concluded that o-hydroxybenzoic acid acquired the most effective redox reaction instead of m-hydroxybenzoic acid and p-hydroxybenzoic acid, resulted in the smaller sized and unaggregated AuNPs. We also confirmed that the hydroxyl group of o-hydroxybenzoic acid, m-hydroxybenzoic acid and p-hydroxybenzoic acid is the functional group responsible for the reduction of Au3+ to Au0. |
topic |
AuNPs o-hydroxybenzoic acid m-hydroxybenzoic acid p-hydroxybenzoic acid |
url |
https://jurnal.ugm.ac.id/ijc/article/view/34440 |
work_keys_str_mv |
AT agustinasusandreani synthesisofgoldnanoparticlescappedbenzoicacidderivativecompoundsioiimiandipihydroxybenzoicacid AT ekosrikunarti synthesisofgoldnanoparticlescappedbenzoicacidderivativecompoundsioiimiandipihydroxybenzoicacid AT srijuarisantosa synthesisofgoldnanoparticlescappedbenzoicacidderivativecompoundsioiimiandipihydroxybenzoicacid |
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