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金纳米粒子催化金属过氧化物复合物氧化水合肼:金纳米粒子表面活性的实验证据。

Gold nano particles catalyzed oxidation of hydrazine by a metallo-superoxide complex: experimental evidences for surface activity of gold nano particles.

机构信息

Department of Chemistry, Jadavpur University, Kolkata 700 032, India.

出版信息

Dalton Trans. 2012 Apr 21;41(15):4641-8. doi: 10.1039/c2dt12191c. Epub 2012 Feb 22.

DOI:10.1039/c2dt12191c
PMID:22354099
Abstract

Gelatin-capped gold nano particles (GNPs) of diameter 23, 28 and 36 nm were prepared and characterized as almost monodispersed, near-spherical solids. In acidic media, these GNPs at their very low concentration level (∼10(-13) M) catalyze the oxidation of hydrazine by the metallo-superoxide, (NH(3))(4)Co(III)(μ-NH(2),μ-O(2))Co(III)(NH(3))(4)(4) (1). In the presence of a large excess of hydrazine over [1], the catalyzed oxidation is first-order in [1], [GNPs] and media alkalinity. The pure first-order dependence implies that the size as well as the nature of the catalyst remained unchanged during the reaction. The catalytic efficacies increased with increased total surface area of the GNPs. Increasing T(Hydrazine) (T(Hydrazine) is the analytical concentration of hydrazine) tends to saturate the first-order rate constant (k(o)) for hydrazine oxidation and a plot of 1/k(o)versus T(Hydrazine) was found to be linear at a particular [GNPs], indicating the GNPs assisted deprotonation of N(2)H(5)(+) to N(2)H(4). The rate constants show a non-linear behavior with temperature studied in the range 288-308 K. At a lower temperature interval, viz. 288-298 K, k(o) increases with increasing temperature whereas at temperature interval, viz. 303-308 K, k(o) decreases with temperature. Such a variation indicates the important process of absorption and desorption of the reactants on and from the surface. A plausible mechanism for the GNPs catalyzed oxidation of hydrazine is suggested.

摘要

直径为 23、28 和 36nm 的明胶包覆金纳米颗粒(GNPs)被制备并被表征为几乎单分散的近球形固体。在酸性介质中,这些 GNPs 在非常低的浓度水平(约 10(-13)M)下,催化金属过氧化物(NH(3))(4)Co(III)(μ-NH(2),μ-O(2))Co(III)(NH(3))(4)(4)(1)氧化联氨。在[1]过量的联氨存在下,催化氧化在[1]、[GNPs]和介质碱度上是一级反应。纯一级依赖关系意味着在反应过程中催化剂的尺寸和性质保持不变。催化效率随 GNPs 的总表面积增加而增加。增加 T(联氨)(T(联氨)是联氨的分析浓度)趋于使联氨氧化的一级速率常数(k(o))饱和,并且在特定[GNPs]下,1/k(o)对 T(联氨)的图是线性的,表明 GNPs 辅助 N(2)H(5)(+)去质子化生成 N(2)H(4)。在 288-308 K 的温度范围内,速率常数表现出与温度的非线性行为。在较低的温度间隔,即 288-298 K,k(o)随温度升高而增加,而在温度间隔,即 303-308 K,k(o)随温度降低而降低。这种变化表明反应物在表面上的吸收和解吸是一个重要的过程。提出了一种 GNPs 催化氧化联氨的可能机制。

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