scholarly journals Glycopolymer Grafted Silica Gel as Chromatographic Packing Materials

2018 ◽  
Vol 20 (1) ◽  
pp. 10 ◽  
Author(s):  
Gaoqi Ma ◽  
Xitao Luo ◽  
Xitong Sun ◽  
Weiyan Wang ◽  
Qinghui Shou ◽  
...  

The modification of the surface of silica gel to prepare hydrophilic chromatographic fillers has recently become a research interest. Most researchers have grafted natural sugar-containing polymers onto chromatographic surfaces. The disadvantage of this approach is that the packing structure is singular and the application scope is limited. In this paper, we explore the innovative technique of grafting a sugar-containing polymer, 2-gluconamidoethyl methacrylamide (GAEMA), onto the surface of silica gel by atom transfer radical polymerization (ATRP). The SiO2-g-GAEMA with ATRP reaction time was characterized by Fourier infrared analysis, Thermogravimetric analysis (TGA), and elemental analysis. As the reaction time lengthened, the amount of GAEMA grafted on the surface of the silica gel gradually increased. The GAEMA is rich in amide bonds and hydroxyl groups and is a typical hydrophilic chromatography filler. Finally, SiO2-g-GAEMA (reaction time = 24 h) was chosen as the stationary phase of the chromatographic packing and evaluated with four polar compounds (uracil, cytosine, guanosine, and cytidine). Compared with unmodified silica gel, modified silica gel produces sharper peaks and better separation efficiency. This novel packing material may have a potential for application with highly isomerized sugar mixtures.

2007 ◽  
Vol 2007 (9) ◽  
pp. 538-540
Author(s):  
Robert D. Guthrie

Silica gel with a variety of surface areas is found to react directly (no SOCl2 treatment required) with butyllithium to give a product with butyl groups attached. The extent of butyl group incorporation depends on available silica surface. With dehydrated 230–400 mesh silica gel, 7.4 mmoles of BuLi per g in pentane added in hexane gave silica with 2.5 mmoles of butyl groups per g provided that the silica gel was washed three times with cold water. It was found that water washing removes some unbutylated silicate increasing the apparent butyl group incorporation. The butyl-modified silica gel showed no chromatographic retention of 3-aminoquinoline in 50:50 hexane: dichloromethane or of thymol in hexane in contrast to unmodified silica gel which is known to strongly retain polar compounds, particularly basic ones. This contrast is demonstrated.


1986 ◽  
Vol 40 (7) ◽  
pp. 1038-1042 ◽  
Author(s):  
R. S. Field ◽  
D. E. Leyden ◽  
R. S. Shreedhara Murthy

A series of standards was prepared by mixing the fluorescein or bromocresol green adsorbed on silica gel modified with N,N-diethylaminopro-pyltriethoxysilane with varying amounts of unmodified silica. Photoacoustic magnitude and phase values were obtained at their respective absorption maxima, 470 and 600 nm. Calibration graphs were prepared by combining the magnitude and phase into the response function. Two-component samples were prepared by mixing the different ratios of the standard samples. The concentration of the dyes in the two-component samples was determined by referring to the respective calibration graphs and solving a pair of simultaneous equations. The relative error in the determination ranged from −5.6% to 5.1% for fluorescein and −16.8% to 38% for bromocresol green when compared to their concentration determined by spectrophotometry.


2000 ◽  
Vol 116 (1) ◽  
pp. 56-61
Author(s):  
Tatsuo YAMAGUCHI ◽  
Toshiaki NAKAI ◽  
Kunihiko TAKEDA

2015 ◽  
Vol 1095 ◽  
pp. 341-344 ◽  
Author(s):  
Can Hui Xu ◽  
Guang Liang Zhang ◽  
Xin Zhou ◽  
Xi Lin Xiao ◽  
Chang Ming Nie ◽  
...  

The characterization of phosphoproteins requires highly specific methods for the separation and enrichment of phosphopeptides. Here we report a novel metal ion-immobilized solid phase material for the separation and enrichment of phosphopeptides. The material is uranyl-salophen-silica gel (USSG) particles in which salophen is a tetradentate ligand of uranyl ion. In USSG salophen is connected on the surface of silica gel and uranyl is bound on the surface through its coordination with salophen. Phosphopeptides can be selectively retained by USSG because uranyl-salophen can bind phosphate moiety with strong affinity and high selectivity. The new material USSG has been successfully used for the separation of phosphopeptides from peptide mixtures with the separation efficiency of 97.0% to 97.4%.


2016 ◽  
Vol 71 (6) ◽  
pp. 1019-1030 ◽  
Author(s):  
Alexander Carreño ◽  
Eduardo Schott ◽  
Ximena Zarate ◽  
Juan Manuel Manriquez ◽  
Juan C. Vega ◽  
...  

2012 ◽  
Vol 2012 ◽  
pp. 1-9 ◽  
Author(s):  
M. Ghaedi ◽  
M. Rezakhani ◽  
S. Khodadoust ◽  
K. Niknam ◽  
M. Soylak

In this research at first palladium nanoparticle attached to a new chemically bonded silica gel has been synthesized and has been characterized with different techniques such as X-ray diffraction (XRD), fourier transform infrared (FT-IR), transmission electron microscopy (TEM), and scanning electron microscopy (SEM). Then, this new sorbent (chemically modified silica gel with N-propylmorpholine (PNP-SBNPM)) was efficiently used for preconcentration of some metal ions in various food samples. The influence of effective variables including mass of sorbent, flow rate, pH of sample solutions and condition of eluent such as volume, type and concentration on the recoveries of understudy metal ions were investigated. Following the optimization of variables, the interfering effects of some foreign ions on the preconcentration and determination of the investigated metal ions described. At optimum values of variables, all investigated metal ions were efficiently recovered with efficiency more than 95%, relative standard deviation (RSD) between 2.4 and 2.8, and detection limit in the range of 1.4–2.7 ng mL−1. The present method is simple and rapidly applicable for the determination of the understudied metal ions (ng mL−1) in different natural food samples.


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