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Capillary column preparation

Fig. 23. Scanning electron micrograph of monolithic capillary column prepared according to [134]... Fig. 23. Scanning electron micrograph of monolithic capillary column prepared according to [134]...
Even if MIP and BET are widely accepted regarding the characterization of HPLC stationary phases, they are only applicable to the samples in the dry state. In order to investigate the impact of polymerization time on the porous properties of wet monolithic columns, ISEC measurements of 200 jm I.D. poly(p-methylstyrene-co-l,2-bis(vinylphenyl)ethane) (MS/BVPE) capillary columns (prepared using a total polymerization time ranging from 45 min to 24 h) have been additionally evaluated (see Table 1.2 for a summary of determined e values). On a stepwise decrease in the time down to 45 min, the total porosity (St) is systematically increasing to about 30% in total (62.8% for 24 h and 97.2% for 45 min). This is caused by a simultaneous increase in the fraction of interparticulate porosity (e. ) as well as the fraction of pores (Cp). The ISEC measurements are in agreement with those of the MIP as well as BET analyses, as an increase in should be reflected in an increase in 8p and as the relative increase in the total porosity (caused by decreasing the polymerization time... [Pg.21]

Figure 8.2 Schematic representation of open tubular capillary column preparation. (Adapted from Ref. 10 with permission.)... Figure 8.2 Schematic representation of open tubular capillary column preparation. (Adapted from Ref. 10 with permission.)...
Another successful example is the separation of a series of steroids listed in Fig. 6.11 using a monolithic capillary column prepared by redox initiated polymerization of a solution of acrylamide 4, methylene bisacrylamide 5, vinylsulfonic acid 12, and dodecyl acrylate 18 in N-methylformamide/TRIS-boric acid buffer (pH 8.2) to which polyethylene glycol) (MW 10,000) was added (overall composition 5% T, 60% C, 10% vinylsulfonic acid, 15% lauryl acrylate, 3% polyethylene glycol)). The capillary tube was first vinylized and its part beyond the detection window was coated with linear polyacrylamide to avoid band broadening. Since laser induced fluorescence was used to decrease the detection limit of the method to about 100 attomoles for neutral steroids, all of the analytes were first tagged with dansylhydrazine. Fig. 6.12 shows an... [Pg.215]

Fig. 6.21. Electrochromatographic separation of benzene derivatives on monolithic capillary column prepared by UV initiated polymerization. Conditions capillary column, 100 pm i.d. x 25 cm active length stationary phase poly(butyl methacrylate-co-ethylene dimethaciylate) with 0.3 wt. % 2-acrylamido-2-methyl-l-propanesulfonic acid pore size, 296 nm mobile phase, 75 25 vol./vol mixture of acetonitrile and 5 mmol/L phosphate buffer pH 7 UV detection at 215 nm 25 kV pressure in vials, 0.2 MPa injection, 5 kV for 3 s. Peaks thiourea (1), benzyl alcohol (2), benzaldehyde (3), benzene (4), toluene (5), ethylbenzene (6), propylbenzene (7), butylbenzene (8), and amylbenzene (9). Fig. 6.21. Electrochromatographic separation of benzene derivatives on monolithic capillary column prepared by UV initiated polymerization. Conditions capillary column, 100 pm i.d. x 25 cm active length stationary phase poly(butyl methacrylate-co-ethylene dimethaciylate) with 0.3 wt. % 2-acrylamido-2-methyl-l-propanesulfonic acid pore size, 296 nm mobile phase, 75 25 vol./vol mixture of acetonitrile and 5 mmol/L phosphate buffer pH 7 UV detection at 215 nm 25 kV pressure in vials, 0.2 MPa injection, 5 kV for 3 s. Peaks thiourea (1), benzyl alcohol (2), benzaldehyde (3), benzene (4), toluene (5), ethylbenzene (6), propylbenzene (7), butylbenzene (8), and amylbenzene (9).
Tests of the reproducibility of retention times, retention factors, separation selec-tivities, and column efficiencies for our methacrylate monolithic capillary columns are summarized in Table 6.2. This table shows averaged data obtained for 9 different analytes injected 14 times repeatedly every other day over a period of 6 days, as well as for 7 different capillary columns prepared from the same polymerization mixture. As expected, both injection-to-injection and day-to-day reproducibilities measured for the same column are very good. Slightly larger RSD values were observed for col-umn-to-column reproducibility. While the selectivity effectively did not change, larger differences were found for the efficiencies of the columns. [Pg.231]

Ji Z, Majors RE, and Guthrie EJ (1999) Porous layer open-tubular capillary columns preparations, applications and future directions. Journal of Chromatography A 842 115-142. [Pg.1833]

A classification of the available methods for adsorption capillary column preparation is presented in Fig. 6-1 [1]. [Pg.183]

The method of adsorption capillary column preparation by means of in situ synthesis of sorbents is only applicable to a limited number of adsorbents, but it does allow two problems to be solved simultaneously 1) sorbent formation 2) binding of a sorbent to the inside surface of capillary. [Pg.240]

IVCOT—wall coated open tubular, a type of capillary column prepared by coating or bonding the inside wall of the capillary with a thin film of stationary phase. [Pg.962]

Time, Cost, and Equipment Analysis time can vary from several minutes for samples containing only a few constituents to more than an hour for more complex samples. Preliminary sample preparation may substantially increase the analysis time. Instrumentation for gas chromatography ranges in price from inexpensive (a few thousand dollars) to expensive (more than 50,000). The more expensive models are equipped for capillary columns and include a variety of injection options and more sophisticated detectors, such as a mass spectrometer. Packed columns typically cost 50- 200, and the cost of a capillary column is typically 200- 1000. [Pg.578]

Gas chromatography (gc) is inferior to hplc in separating abiUty. With gc, it is better to use capillary columns and the appHcation is then limited to analysis (67). Resolution by thin layer chromatography or dc is similar to Ic, and chiral stationary phases developed for Ic can be used. However, tic has not been studied as extensively as Ic and gc. Chiral plates for analysis and preparation of micro quantities have been developed (68). [Pg.279]

Typical operating conditions by GC and HPLC are listed in Tables 2 and 3, respectively. Anilides are separated using a weakly polar liquid-phase capillary column, such as SPB-1 or HP-5, which is prepared based on 5% diphenyl-95% dimethylpolysilox-ane for GC. For HPLC, ODS columns are used. [Pg.332]

Slurry packing techniques are required for the preparation of efficient columns with rigid particles of less than 20 micrometers in diameter. The same general packing apparatus. Figure 4.8, can be used to pack columns by the balanced-density slurry, liquid slurry, or the viscous slurry techniques. Down-fill slurry packing is the method of choice for small bore columns and packed capillary columns. [Pg.180]

Before discussing column preparation procedures a few comments on nomenclature are in order. Open tubular columns are also widely known as capillary columns. The characteristic feature of these columns is their openness, which provides an unrestricted gas path through the column. Thus open tubular colximn rather than capillary column is a more apt description. However, both descriptions appear frequently in the literature and can be emsidered interchangeable. The type of columns discussed so far are also known as wall-coated open tubular columns (WCOT). Here the liquid phase is deposited directly onto the column wall without the inclusion of any additive that might be considered as... [Pg.590]


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