scholarly journals Nanostructured Silver Coating as a Stationary Phase for Capillary Gas Chromatography

Molecules ◽  
2019 ◽  
Vol 24 (24) ◽  
pp. 4491
Author(s):  
Qiong Jiang ◽  
Peng Xu ◽  
Juanjuan Feng ◽  
Min Sun

A capillary column coated with nanostructured silver coating was fabricated for gas chromatography. The nanostructured silver coating, about 80–120 nm in thickness, was prepared as the stationary phase via silver mirror reaction, and was characterized by SEM and EDS. The column was evaluated using different types of model analytes, including n-alkanes, n-alcohols, benzenes, and Grob mixture. A baseline separation of ten n-alkanes on the silver column (15 m × 0.20 mm i.d.) was achieved within 3.5 min through the main hydrophobic mechanism. A mixture of six n-alcohols, or another mixture containing three butanol isomers and two octanol isomers, was separated well on the column. The column separated some benzenes containing benzene, toluene, ethylbenzene, p-xylene, o-xylene, styrene, benzaldehyde, and benzyl alcohol. A Grob mixture containing seven analytes was also separated successfully. Based on a multiple retention mechanism such as hydrophobic, dipole-dipole, and dipole-induced dipole interactions, the silver column achieved a good separation of twelve different types of compounds within 2.5 min. The column presented satisfactory separation repeatability with relative standard deviation of retention time between 0.073% and 0.591%. The results indicate that the silver column is promising for gas chromatographic separation.

RSC Advances ◽  
2015 ◽  
Vol 5 (93) ◽  
pp. 76007-76013 ◽  
Author(s):  
Yingzhen Wang ◽  
Meiling Qi ◽  
Ruonong Fu

The binary stationary phase of CB7 in an ionic liquid shows high selectivity and resolving ability for diverse analytes via multiple molecular interactions and unique retention mechanism.


1985 ◽  
Vol 63 (11) ◽  
pp. 2824-2828 ◽  
Author(s):  
T. Jayalakshmi ◽  
Kalluru S. Reddy

Excess volumes for the binary liquid mixtures of methylisobutylketone with benzene, toluene, chlorobenzene, bromobenzene, and nitrobenzene have been measured at 303.15 and 313.15 K. Excess volumes were negative for all the systems over the entire range of composition and at both the temperatures. The behaviour of VE as a function of composition and temperature was studied. Viscosity data have also been determined for the five systems at 303.15 K. The excess viscosity, Δ ln η, has been calculated and its behaviour as a function of composition was investigated. The results of VE and Δ ln η have been discussed in terms of dipole – induced dipole and dipole–dipole interactions between the components. VE and Δ ln η were analysed in the light of Prigogine–Patterson–Flory equation of state theory and Bloomfield and Dewan's viscosity relations.


2007 ◽  
Vol 90 (6) ◽  
pp. 1670-1676 ◽  
Author(s):  
Jose Fenoll ◽  
Pilar Hellin ◽  
Josefa Lopez ◽  
Alberto Gonzalez ◽  
Pilar Flores

Abstract A sensitive, rapid, and simple multiresidue method for the simultaneous determination of 19 pesticides in different varieties of lettuce (Lactuca sativum) was developed. Lettuce samples were extracted by homogenization with acetone and partitioned into ethyl acetatecyclohexane. Subsequent sample cleanup was not needed. Final determination was made by capillary gas chromatography (GC) with electron-capture detection (ECD). Confirmation analysis of pesticides was performed by GC coupled with mass spectrometry in the selected ion monitoring mode. The average recovery by the GCECD method obtained for these compounds varied from 66.4 to 119.2 with relative standard deviations <7.7. The GCECD method has good linearity, and the detection limit for the pesticides studied varied from 0.1 to 3.8 g/kg. The proposed method was used to determine pesticide levels in different types of lettuce grown in soils from experimental fields.


2014 ◽  
Vol 32 (10) ◽  
pp. 1117
Author(s):  
Gang CHEN ◽  
Xiaojie ZHAO ◽  
Jun XING ◽  
Yuhua YAO ◽  
Jingjing ZHENG

1973 ◽  
Vol 19 (1) ◽  
pp. 109-112 ◽  
Author(s):  
Mohammed Tajuddin ◽  
Stanley G Elfbaum

Abstract The N,O-dipivalyl methyl esters of triiodothyronine and thyroxine were prepared and gas chromatographed. "Dexsil 300 GC," a heat-stable polycarboranesiloxane, was used as the stationary phase. Separations were good and prompt. As little as 250 pg of triiodothyronine was detectable. Dexsil 300 GC was used satisfactorily in measuring serum triiodothyronine


1965 ◽  
Vol 48 (4) ◽  
pp. 694-699
Author(s):  
David M Takahashi

Abstract Antioxidants (BHA and BHT) in different types of breakfast cereals were studied by argon ionization gas chromatography. Samples containing antioxidants were packed into the column, and antioxidants were eluted with redistilled petroleum ether. EIuates were concentrated under N2 and injected into a Barber-Colman Model 10 gas chromatograph. Recoveries ranged from about 92 to 110%. Results obtained by steam distillation-colorimetry methods were erratic. Colorimetric procedures were not free from interferences and could lead to highly erroneous results at the lower ppm levels. The gas chromatographic method is faster, simpler, and more accurate. Collaborative studies on corn and rice ready-to-eat breakfast cereals are recommended.


2006 ◽  
Vol 61 (5-6) ◽  
pp. 341-346 ◽  
Author(s):  
Jae-Woo Park ◽  
A. M. Abd El-Aty ◽  
Myoung-Heon Lee ◽  
Sung-Ok Song ◽  
Jae-Han Shim

A multiresidue method for the simultaneous determination of 22 organochlorine (OCs) and organophosphorus (Ops) pesticides (including isomers and metabolites), representing a wide range of physicochemical properties, was developed in fatty matrices extracted from meat. Pesticides were extracted from samples with acetonitrile/n-hexane (v :v, 1:1). The analytical screening was performed by gas chromatography coupled with electron-capture detection (ECD). The identification of compounds was based on their retention time and on comparison of the primary and secondary ions. The optimized method was validated by determining accuracy (recovery percentages), precision (repeatability and reproducibility), and sensitivity (detection and quantitation limits) from analyses of samples fortified at 38 to 300 ng/g levels. Correlation coefficients for the 22 extracted pesticide standard curves (linear regression analysis, n = 3) ranged from 0.998 to 1.000. Recovery studies from 2 g samples fortified at 3 levels demonstrated that the GC-ECD method provides 64.4-96.0% recovery for all pesticides except 2,4′-DDE (44.6-50.4%), 4,4′-DDE (51.1-57.5%) and 2,4′-DDT (50.0-51.2%). Both repeatability and reproducibility relative standard deviation values were < 20% for all residues. Detection limits ranged from 0.31 to 1.27 ng/g and quantification limits were between 1.04 and 4.25 ng/g. The proposed analytical method may be used as a simple procedure in routine determinations of OCs and Ops in meat. It can also be applied to the determination of pesticide multi-residues in other animal products such as butter and milk.


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