摘要
This paper reports the chitosan-mediated synthesis of porous hematite nanoparticles with FeCl3 as the precursor via a hydrothermal approach at 160℃.A series of porous chitosan/iron oxide hybrid nanoparticles were obtained via changing the ratio of chitosan to FeCl3,FeCl3 concentration and pH value of the reaction solution,and producing porous iron oxide nanoparticles after calcination.The as-prepared samples were characterized by means of X-ray diffraction,transmission electron microscopy,thermal gravimetric analysis,Fourier transform infrared,and N2 sorption.The particle sizes of these metal oxides were less than 100 nm,and the pore sizes were in the range of 2-16 nm.It was demonstrated that chitosan played a key role in the formation of the porous structures.The resultant α-Fe2O3 nanoparticles were used as the support to immobilize Au or Pd nanoparticles,producing Au/α-Fe2O3 or Pd/α-Fe2O3 nanoparticles.The as-prepared α-Fe2O3 nanocatalyst exhibited high selectivity towards cyclohexanone and cyclohexanol for catalyzing cyclohexane oxidation with O2 at 150℃.
This paper reports the chitosan-mediated synthesis of porous hematite nanoparticles with FeCl3 as the precursor via a hydrothermal approach at 160℃.A series of porous chitosan/iron oxide hybrid nanoparticles were obtained via changing the ratio of chitosan to FeCl3,FeCl3 concentration and pH value of the reaction solution,and producing porous iron oxide nanoparticles after calcination.The as-prepared samples were characterized by means of X-ray diffraction,transmission electron microscopy,thermal gravimetric analysis,Fourier transform infrared,and N2 sorption.The particle sizes of these metal oxides were less than 100 nm,and the pore sizes were in the range of 2-16 nm.It was demonstrated that chitosan played a key role in the formation of the porous structures.The resultant α-Fe2O3 nanoparticles were used as the support to immobilize Au or Pd nanoparticles,producing Au/α-Fe2O3 or Pd/α-Fe2O3 nanoparticles.The as-prepared α-Fe2O3 nanocatalyst exhibited high selectivity towards cyclohexanone and cyclohexanol for catalyzing cyclohexane oxidation with O2 at 150℃.
基金
supported by the Ministry of Science and Technology of China (2009CB930802)
the Chinese Academy of Sciences (KJCX2.YW.H16)
