Synthesis and hydrogen production kinetics of temperature-responsive aluminum-poly(N-isopropylacrylamide) core-shell nanoparticles

被引:1
作者
Zeng, Wenhui [1 ]
Jelliss, Paul A. [1 ]
Buckner, Steven W. [1 ]
机构
[1] St Louis Univ, Dept Chem, St Louis, MO 63103 USA
关键词
Aluminum nanoparticles; Thermoresponsive polymer; Non-Arrhenius hydrolysis; DELAFOSSITE CUALO2 NANOPARTICLES; ALUMINUM NANOPARTICLES; GOLD NANOPARTICLES; POLY(N-ISOPROPYLACRYLAMIDE) GELS; POLY(METHYL METHACRYLATE); N-ISOPROPYLACRYLAMIDE; TRANSITION; COPOLYMERS; STABILITY; CHEMISTRY;
D O I
10.1016/j.matchemphys.2018.08.081
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
We report here on the synthesis of air-stable aluminum nanoparticles (Al NPs) capped with a temperature-responsive polymer, poly(N-isopropylacrylamide) (PNIPAM). These core-chell particles display temperature-dependent hydrogen production kinetics upon hydrolysis. Kinetic studies show that the bimolecular rate constant below the critical solution temperature (CST) is 2.85 x 10(-4) L mol(-1) s(-1) (at 20 degrees C), which is nearly twice that of the rate constant (1.6 x 10(-4) L mol(-1) s(-1)) above the CST (at 40 degrees C). This non-Arrhenius behavior is proposed to originate from collapse of the capping layer above the CST which creates a less permeable capping layer. The core-shell nanoparticles were characterized with powder X-ray diffraction (PXRD), Fourier transform infrared spectroscopy with total attenuated reflection (FTIR-ATR), and differential scanning calorimetry coupled with thermogravimetric analysis (DSC/TGA). Transmission electron microscopy (TEM) confirms the Al NPs are core-shell structures and the composite particle size distribution ranges from 22 nm to 40 nm.
引用
收藏
页码:233 / 239
页数:7
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