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通过混合表面活性剂介导的方法合成高比表面积羟基磷灰石纳米颗粒。

Synthesis of high surface area hydroxyapatite nanoparticles by mixed surfactant-mediated approach.

作者信息

Uota Masafumi, Arakawa Hiroshi, Kitamura Nana, Yoshimura Takumi, Tanaka Junzo, Kijima Tsuyoshi

机构信息

CREST, Japan Science and Technology Cooperation, 4-1-8 Honcho, Kawaguchi, Saitama 332-0012, Japan.

出版信息

Langmuir. 2005 May 10;21(10):4724-8. doi: 10.1021/la050029m.

Abstract

A new surfactant-mediated approach was developed to synthesize hydroxyapatite (HAp) nanoparticles with high surface areas by calcination of their precursors encapsulated with calcium stearate using mixed surfactant-containing reaction mixtures. Acidic aqueous solution of calcium phosphate was mixed with both or either nonaoxyethylene dodecyl ether (C12EO9) and polyoxyethylene(20) sorbitan monostearate (Tween 60) and then was treated with aqueous ammonium at 25 degrees C. The C12EO9-based single surfactant system yielded an aggregate of platy HAp nanoparticles 20-40 nm in size, whereas the Tween 60-based single and mixed systems led to lath-shaped HAp nanoparticles 2-8 nm wide and encapsulated with calcium stearate. On calcination at 500 degrees C, the stearate-encapsulated HAp nanoparticles in the latter two systems were deorganized into high surface area HAp nanoparticles. Particularly, the HAp nanoparticles in the mixed system exhibited a specific surface area as high as 364 m2 g(-1) that is roughly 3 times larger than 160 m2 g(-1) for those in the single system. The significantly high surface area for the former is attributed to much less adhesion of decapsulated HAp nanoparticles, which originated from the particle-separating effect of the C12EO9 molecules adsorbed on the outer surface of the stearate-encapsulated HAp nanoparticles to inhibit their agglomeration or interfacial coordination. The present results demonstrate that the mixed use of two different surfactants as a source of encapsulating and templating agent and a particle-separating agent is specifically effective for the synthesis of high surface area HAp nanoparticles.

摘要

开发了一种新的表面活性剂介导的方法,通过煅烧用硬脂酸钙包裹的前驱体来合成具有高表面积的羟基磷灰石(HAp)纳米颗粒,使用含混合表面活性剂的反应混合物。将酸性磷酸钙水溶液与九氧乙烯十二烷基醚(C12EO9)和聚氧乙烯(20)山梨醇单硬脂酸酯(吐温60)中的一种或两种混合,然后在25℃下用氨水进行处理。基于C12EO9的单一表面活性剂体系产生了尺寸为20-40nm的片状HAp纳米颗粒聚集体,而基于吐温60的单一和混合体系则产生了宽度为2-8nm且被硬脂酸钙包裹的板条状HAp纳米颗粒。在500℃煅烧时,后两种体系中被硬脂酸酯包裹的HAp纳米颗粒会解聚成高表面积的HAp纳米颗粒。特别地,混合体系中的HAp纳米颗粒表现出高达364 m2 g(-1)的比表面积,约为单一体系中HAp纳米颗粒比表面积160 m2 g(-1)的3倍。前者显著高的比表面积归因于解包封的HAp纳米颗粒的粘附力小得多,这源于吸附在硬脂酸酯包裹的HAp纳米颗粒外表面的C12EO9分子的颗粒分离作用,从而抑制了它们的团聚或界面配位。目前的结果表明,将两种不同的表面活性剂混合用作包封和模板剂以及颗粒分离剂,对于合成高表面积的HAp纳米颗粒特别有效。

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