As reported in our previous study [

As reported in our previous study [32], mesoporous silicananoparticles
(MSN) were rapidly synthesized via hydrolysis and co-condensation
of TEOS and C18TMS in an ethanol-water-ammonia system. The
detailed procedures were as follows: C18TMS and TEOS were first dissolved
in 50 mL EtOH and sonicated for 10 min, then the mixture was
added into the solutions containing ethanol, deionized water and ammonia.
Here, different C18TMS/TEOS molar ratios (0.32, 0.53, 0.74) and
EtOH/H2O volume ratios (3.6, 5.6, 7.5) were used to tune the pore size
ofMSN. After the mixturewas stirred for 2 h at 25 °C, the solid products
were collected by filtration, washed with deionized water for several
times, and dried at room temperature in air. Finally, the resulted silica/
surfactant composite powder was calcined at 550 °C for 6 h to obtain
MSN.
The scanning electron microscopy (SEM) images were obtained
using a Hitachi S-4800 microscope operated at an acceleration voltage

ผลลัพธ์ (อังกฤษ) 2:

As reported in our previous Study [32], mesoporous Silicananoparticles
(MSN) were rapidly synthesized via hydrolysis and co-Condensation
of TEOS and C18TMS in an ethanol-ammonia-Water System. The
detailed procedures were as follows: First C18TMS and TEOS were Dissolved
in 50 mL EtOH and sonicated for 10 min, then the mixture was
added Into the Solutions containing ethanol, deionized Water and ammonia.
Here, different C18TMS / TEOS Molar ratios (0.32, 00:53, 0.74) and
EtOH / H2O volume ratios (3.6, 5.6, 7.5) were used to Tune the Pore Size
OfMSN. After the Mixturewas stirred at 25 ° C for 2 H, the Solid Products
were Collected by Filtration, washed with deionized Water for several
times, and at Room Temperature in Air Dried. Finally, the resulted Silica /
surfactant composite was calcined at 550 ° C for Powder 6 H to obtain
MSN.
Scanning Electron microscopy the (SEM) images were obtained
using a Hitachi S-4800 Microscope operated at an acceleration Voltage.