Surface Modification of Inorganic Nanoparticles by Organic Functional Groups

Author(s):  
Seiichi Takami
NANO ◽  
2009 ◽  
Vol 04 (06) ◽  
pp. 367-370 ◽  
Author(s):  
A. DULDA ◽  
D. S. JO ◽  
M. TAKAKI ◽  
D. H. YOON

Surface modification of luminescent nanomaterials has attracted considerable technological interest. With decreasing particle size, the passivation of surface defects is of vital importance. This paper reports the effect of an alkali (KOH) solution treatment and organic functional groups on the luminescence efficiency and particle dispersibility. Fourier transform infrared spectroscopy provided clear evidence of surface modification with organic functional groups from the C=O , C–H , and C–O stretching modes at 1740, 1365, and 1218 cm-1. The KOH-treated sample showed a 40% increase in luminescence intensity, whereas 87% increase in luminescence intensity was obtained from the dispersion-agent-containing sample. To the best of our knowledge, this is the highest efficiency improvement for sub-micrometer-sized BAM: Eu2+ phosphors reported thus far.


RSC Advances ◽  
2014 ◽  
Vol 4 (52) ◽  
pp. 27201-27206 ◽  
Author(s):  
Masaki Kitahara ◽  
Kazuyuki Kuroda

We demonstrate a sophisticated and unique method of Au deposition exclusively inside mesoporous silica, in clear contrast to conventional methods requiring surface modification with organic functional groups interacting with Au.


2012 ◽  
Vol 538-541 ◽  
pp. 350-353 ◽  
Author(s):  
Shou Wu Yu ◽  
Shu Juan Xiao ◽  
Xiao Ming Sang ◽  
Gui Xiang Hou

The surface of commercial TiO2 nanoparticles was modified by titanate coupling agent, JSC(isopropyl tricarboxytate titanate), FTIR spectrum confirmed that organic functional groups were successfully grafted onto the surface of TiO2 nanoparticles. The SEM micrographs indicated that the aggregation of modified TiO2 was reduced and most of the particles were approximately 20 nm.


Complexity ◽  
2006 ◽  
Vol 11 (3) ◽  
pp. 9-10 ◽  
Author(s):  
Harold J. Morowitz ◽  
Vijayasarathy Srinivasan ◽  
Eric Smith

1969 ◽  
Vol 57 (4) ◽  
pp. 821-825 ◽  
Author(s):  
Walter L. Nazimowitz ◽  
T. S. Ma

2014 ◽  
Vol 70 (2) ◽  
Author(s):  
Sutthisa Konruang ◽  
Thawat Chittrakarn ◽  
Suksawat Sirijarukul

The effects of ultraviolet (UV) irradiation for surface modification of hydrophobic asymmetric polysulfone membranes have been investigated. The asymmetric polysulfone (PSF) membranes were prepared by phase inversion method using 19%-25% of PSF in two solvents, viz. dimethylacetamide (DMF) and Acetone (Ac) collectively. The surface of asymmetric polysulfone membranes were modified by UV ray with 254 and 312 nm wavelength. Chemical and physical properties of the untreated and the treated membranes were characterized. Scanning electron microscope (SEM) was used to determine asymmetric structure of polysulfone membranes. Contact angle device was used to analyzed the effected of UV ray treatment on hydrophilicity of membranes surface. Polar functional groups introduced by UV irradiation were examined using FTIR. The water flux was measured under a pressure of 500 kPa to 2,500 kPa with a feed temperature of 25°C. It was shown that asymmetric polysulfone membranes were produced and the UV ray treatment significantly alters the hydrophilicity of membranes surface indicated by the reduction of water contact angle with increasing treatment time. The FTIR analysis showed the formations of polar functional groups such as hydroxyl and carbonyl groups. Consequently, the surface of asymmetric polysulfone membranes was changed from hydrophobic to hydrophilic by UV irradiation leading to the enhancement of the water flux.


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