The Analysis of volatile compounds by purge and trap with whole column cryotrapping (WCC) on a fused silica capillary column

The purge and trap (P&T) method of analysis has been interfaced with fused silica capillary column gas chromatography. This interfacing has been accomplished without splitting the P&T trap desorption carrier gas. Thus, 100% of the purged compounds are transferred to the column. The analytes are cryofocussed on the column using whole column cryotrapping (WCC) at ?80°C. The resulting P&T/WCC procedure is extremely well-suited to the analysis of trace purgeable aqueous organic compounds. Samples and standards containing a variety of aromatic standard compounds were analyzed. The standards included benzene, toluene, ethylbenzene, xylenes, C₃-C₄-benzenes, and naphthalene, as well as three P&T internal standard compounds. Chromatographic peak widths were uniformly less than 6 s at the base and excellent precision was obtained in the relative retention time data for all compounds. The chromatogram of a groundwater sample contaminated with aromatic gasoline compounds is also presented. Since P&T/WCC works well with fused silica capillary columns, the full sensitivity and chromatographic efficiency of capillary gas chromatography is made available to P&T analyses.     

Effects of trapping temperature and film thickness in purge and trap with whole column cryotrapping on fused silica columns

The effects of trapping temperature and column film thickness were investigated with respect to their ability to promote effective cryofocusing on fused silica capillary columns. The study was a further development of the purge and trap with whole column cryotrapping (P&T/WCC) method. The rates at which compounds could be thermally desorbed from a P&T unit and transferred to a column (with zero split) were first examined. A near quantitative transfer of the desorbable analytes was obtained with a 4 min, 180°C, 20 mL/min desorption. The compounds tested included naphthalene. Columns with film thicknesses from 0.12 to 3.0 μm were then investigated in P&T/WCC analyses with WCC temperatures ranging from ?80 to 0°C. The trapping took place from a transfer line gas stream initially at 175°C. The volatilities of the compounds examined varied from that of 1,1-dichloroethene to 1,1,2,2-tetrachloroethane. A higher film thickness was found to ease the WCC temperature requirements. Within each column type, the warmest WCC temperatures which allowed good cryotrapping with no significant increases in peak width were: 0.25 μm, ?70°C; 1.0 μm, ?50°C; 3.0 μm, ?20°C. In addition to being quantitative, the trapping provided good chromatography.     

Deactivation of fused silica capillary columns with phenylhydrosiloxanes

In this work, an investigation of new organosilicon hydride reagents with phenyl functional groups for deactivation and surface modification of fused silica capillary columns is described. Different reagents were tested for their ability to deactivate the fused silica surface, and actual critical surface tension measurements were made using the capillary rise method. The deactivation procedure required lower optimum temperatures than conventional methods. Deactivated capillaries and coated capillary columns were prepared and tested for reproducibility, efficiency, and surface inertness towards basic and acidic compounds at the low nanogram level.     

Hydrothermal treatment of fused silica capillary columns

The activity of fused silica capillary tubing has been shown to vary considerably, which severely influences the reproducibility of column deactivation and inertness. Methods for producing a reproducible, high activity surface with maximum hydroxylation by various hydrothermal treatments were evaluated. Columns pretreated with 20% nitric acid at 200°C for 10 hours, deactivated with D₄, coated with OV-73, and crosslinked with azo-tert-butane were found to possess excellent inertness for sensitive analytes such as alcohols, amines, and alkaloid drugs.     

Deactivation of fused silica capillary columns with cyanopropylhydrosiloxanes

A method is described for surface deactivation and modification of fused silica capillary columns with a cyanopropyl-containing reagent. The deactivation procedure involved a dehydrocondensation reaction between a bis(cyanopropyl)methylhydropolysiloxane reagent and surface silanol groups at an optimum temperature of only 250°C. Actual critical surface tension measurements were made using the capillary rise method. Excellent deactivation for acidic and basic compounds at the low ng level, and wettability for nonpolar and polar polysiloxane stationary phases were obtained. A procedure was developed to remove acidic impurities that are present in polar stationary phases.     

Analysis of toxic anthraquinones and related compounds with a fused silica capillary column

In this study, application of a fused silica capillary column for analysis of toxic anthraquinones and related compounds found in plants was investigated.     

Fused silica capillary micro-packed columns in gas chromatography

Summary Flexibility, strength and adsorption inertness of fused-silica capillaries permits their extensive application for the preparation of micro-packed columns in gas chromatography. Decreasing the column diameter (from 0.5 to 0.15 mm) and the diameter of the sorbent particles (from 100 to 5 μm) results in a marked reduction of the height equivalent to a theoretical plate (HETP), as well as in diminishing the dependence of the HETP on the carrier gas flow rate. The chromatographic characteristics of fused-silica capillary micro-packed columns and open-tubular columns are compared. The fused-silica capillary micro-packed column can be used to advantage for performing rapid and trace analyses and have been shown to be adapted for application in gas-solid chromatography. Separation of organic and inorganic compounds on fused-silica capillary micro-packed columns is illustrated by practical examples. Presented at the 15th International Symposium on Chromatography, Nürnberg, October 1984     

A study of some deactivation methods for fused silica capillary columns by CP-MAS NMR and capillary gas chromatography

The effect of deactivating a fused silica surface by silylation with 1,1,3,3-tetraphenyl-1,3-dimethylilazane (TPDMDS), triphenylsilylamine (TPSA), and octamethylcyclotetrasiloxane (D4) and by polydimethylsiloxane degradation (PSD) is studied. Rehydrated, dried, and deactivated Cab-O-Sil M5 samples are used as model materials for ²⁹Si CP-MAS NMR analysis. At about 350 °C, TPDMDS yelds mainly diphenylmethylsiloxysilane, dimethyldisiloxysilane, and triphenylsiloxysilane groups. TPSA yields phenyltrisiloxysilane, diphenyldisiloxysilane, and triphenylsiloxysilane groups. At 400°C, the products formed initially are eventually replaced by methyltrisiloxysilane or phenyltrisiloxysilane groups, while a substantial number of silanol groups still remains. The possible consequences for wettability are discussed. D4 reacts with Cab-O-Sil even at 200°C, but a large number of silanol groups remains. This number decreases gradually at higher temperatures and becomes negligible above 400°C. The formation of methyltrisiloxysilane groups, which starts at 425°C, is predominant at 490°C.     

Analysis of mutagenic amino acid pyrolyzates with a fused silica capillary column

In this study, application of a fused silica capillary column for analysis of major mutagenic heterocyclic compounds found in cooked foods was investigated.     

On the stability of micro-LC columns (packed fused silica capillary columns)

The life expectancy and resistance to flow, pressure shocks, solvent gradients, and bending of packed fused silica capillary columns (Micro-LC) are discussed.     

Novel fused silica capillary columns: Surface modification through controlled doping of the preform-tube

A method has been developed for fabricating fused silica capillary columns which have specific surface properties but still retain the excellent strength, flexibility, and resilience of pure fused silica. By using the Modified Chemical Vapor Deposition process (MCVD), typically used for the production of optical fiber lightguides, inorganic dopants such as Al, Nd, Ge, and P can be introduced into the preform-tube by MCVD. Doped columns have a wide range of specific surface properties, and columns with undoped fused silica prepared by MCVD are more chemically inert and less acidic than columns prepared by conventional methods. This paper describes the method for fabricating capillaries and the initial studies to characterize them.