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Chromatography chromatogram resolution

The general elution problem in chromatography. Improving the resolution of the overlapping bands in chromatogram (a) results in a longer analysis time for chromatogram (b). [Pg.558]

Figure 6.5 shows a chromatogram of Epikote 1004 using the KE-600 series and SYSTEM-24H (a newly developed GPC system used with the KF-600 series for full utilization of the efficiency of the downsized columns). Compared with conventional-sized columns such as the KF-800 series, the time of analysis is shortened to one-half and the chromatographie resolution is improved. [Pg.181]

Figure 10.3 Gas cliromatograms of a cold-pressed lemon oil obtained (a) with an SE-52 column in the stand-by position and (b) with the same column showing the five heart-cuts (c) shows the GC-GC chiral chromatogram of the ti ansfeired components. The asterisks in (b) indicate electric spikes coming from the valve switcliing. The conditions were as follows SE-52 pre-column, 30 m, 0.32 mm i.d., 0.40 - 0.45 p.m film tliickness cairier gas He, 90 KPa (stand-by position) and 170 KPa (cut position) oven temperature, 45 °C (6 min)-240 °C at 2 °C/min diethyl-tert-butyl-/3-cyclodextrin column, 25 m X 0.25 mm i.d., 0.25 p.m film thickness cairier gas He, 110 KPa (stand-by position) and 5 KPa (cut position) oven temperature, 45 °C (6 min), rising to 90 °C (10 min) at 2 °C/min, and then to 230 °C at 2 °C/min. Reprinted from Journal of High Resolution Chromatography, 22, L. Mondello et al, Multidimensional capillary GC-GC for the analysis of real complex samples. Part IV. Enantiomeric distribution of monoterpene hydrocarbons and monoterpene alcohols of lemon oils , pp. 350-356, 1999, with permission from Wiley-VCH. Figure 10.3 Gas cliromatograms of a cold-pressed lemon oil obtained (a) with an SE-52 column in the stand-by position and (b) with the same column showing the five heart-cuts (c) shows the GC-GC chiral chromatogram of the ti ansfeired components. The asterisks in (b) indicate electric spikes coming from the valve switcliing. The conditions were as follows SE-52 pre-column, 30 m, 0.32 mm i.d., 0.40 - 0.45 p.m film tliickness cairier gas He, 90 KPa (stand-by position) and 170 KPa (cut position) oven temperature, 45 °C (6 min)-240 °C at 2 °C/min diethyl-tert-butyl-/3-cyclodextrin column, 25 m X 0.25 mm i.d., 0.25 p.m film thickness cairier gas He, 110 KPa (stand-by position) and 5 KPa (cut position) oven temperature, 45 °C (6 min), rising to 90 °C (10 min) at 2 °C/min, and then to 230 °C at 2 °C/min. Reprinted from Journal of High Resolution Chromatography, 22, L. Mondello et al, Multidimensional capillary GC-GC for the analysis of real complex samples. Part IV. Enantiomeric distribution of monoterpene hydrocarbons and monoterpene alcohols of lemon oils , pp. 350-356, 1999, with permission from Wiley-VCH.
Figure 12.1 Analysis of Tinuvin 1577 in 30% virgin olive oil (in hexane), showing (a) the gas cliromatogram comparing the pure oil with a sample at the Tinuvin 1577 detection limit concentration, and (b) the coixesponding liquid chromatogram. Reprinted from Journal of High Resolution Chromatography, 20, A. L. Baner and A. Guggenberger, Analysis of Tinuvin 1577 polymer additive in edible oils using on-line coupled HPLC-GC , pp. 669-673, 1997, with pennission from Wiley-VCH. Figure 12.1 Analysis of Tinuvin 1577 in 30% virgin olive oil (in hexane), showing (a) the gas cliromatogram comparing the pure oil with a sample at the Tinuvin 1577 detection limit concentration, and (b) the coixesponding liquid chromatogram. Reprinted from Journal of High Resolution Chromatography, 20, A. L. Baner and A. Guggenberger, Analysis of Tinuvin 1577 polymer additive in edible oils using on-line coupled HPLC-GC , pp. 669-673, 1997, with pennission from Wiley-VCH.
Figure 15.12 GC-GC chromatogram of a natural cw-3-hexen-l-ol fraction. Peak identification is as follows 1, ethyl-2-methylbutyrate 2, traw-2-hexenal 3, 1-hexanol 4, cw-3-hexen-l-ol 5, tro 5-2-hexen-l-ol. Adapted from Journal of High Resolution Chromatography, 15, S. Nitz et al.. Multidimensional gas chromatography-isotope ratio mass specti ometry, (MDGC-IRMS). Part A system desaiption and technical requuements , pp. 387-391, 1992, with permission from Wiley-VCH. Figure 15.12 GC-GC chromatogram of a natural cw-3-hexen-l-ol fraction. Peak identification is as follows 1, ethyl-2-methylbutyrate 2, traw-2-hexenal 3, 1-hexanol 4, cw-3-hexen-l-ol 5, tro 5-2-hexen-l-ol. Adapted from Journal of High Resolution Chromatography, 15, S. Nitz et al.. Multidimensional gas chromatography-isotope ratio mass specti ometry, (MDGC-IRMS). Part A system desaiption and technical requuements , pp. 387-391, 1992, with permission from Wiley-VCH.
Figure 7.27 Constructed Gram-Schmidt chromatogram of a temperature-programmed packed-capillary LC separation of 4.8 ig Irgafos P-EPQ dissolved in DMF temperature programme 50°C for 8min, 4°Cmin-1 up to 140°C. Legend 1, mono-P-EPQ 2, Irgafos 168 3, 4,3 -P-EPQ 4, oxidised 4,4 -P-EPQ 5, 4,4 -P-EPQ. After Bruheim et al. [511]. From I. Bruheim et al., Journal of High Resolution Chromatography, 23, 525-530 (2000). Wiley-VCH, 2000. Reproduced by permission of Wiley-VCH. Figure 7.27 Constructed Gram-Schmidt chromatogram of a temperature-programmed packed-capillary LC separation of 4.8 ig Irgafos P-EPQ dissolved in DMF temperature programme 50°C for 8min, 4°Cmin-1 up to 140°C. Legend 1, mono-P-EPQ 2, Irgafos 168 3, 4,3 -P-EPQ 4, oxidised 4,4 -P-EPQ 5, 4,4 -P-EPQ. After Bruheim et al. [511]. From I. Bruheim et al., Journal of High Resolution Chromatography, 23, 525-530 (2000). Wiley-VCH, 2000. Reproduced by permission of Wiley-VCH.
The cycloalkylcarbamates do not absorb UV light above 220 nm and therefore can be used as the CSPs for thin-layer chromatography (TLC).191 The TLC chromatogram was readily detected by UV radiation at 254 nm and showed the resolution of racemates into each enantiomer. The TLC results can be compared with those obtained by HPLC with the same CSP. The a values in HPLC are slightly larger than those in TLC, although a good correlation is observed between these a values. The cycloalkylcarbamates can be very useful CSPs for TLC as well as for HPLC resolution. [Pg.181]

The modern analytical laboratory employing instrumental chromatography uses a computer data collection system and associated software to acquire the data and display the chromatogram on the monitor. Parameters important for qualitative and quantitative analysis, including retention times and peak areas, are also measured and displayed. The software can also analyze the data to determine resolution, capacity factor, theoretical plates, and selectivity. [Pg.325]

Figure 19.7. Cyclic batch elution chromatography obtaining high product purity and high throughput by using incomplete resolution (overlapping bands) and recycling the mixed fraction (mf) to the feedstock (a) Control of band separation and cut points determines fractional impurities t mij mr and Ami /mr2-<4l)> (b) Chromatogram for separation of pure ds- and trans- 1,3-pentadiene. Components 1, isoprene 2, trans- 1,3-pentadiene 3, cis-l,3-pentadiene 4, cyclo-pentadiene. Component 1 is eluted at almost the same time as component 4 of the... Figure 19.7. Cyclic batch elution chromatography obtaining high product purity and high throughput by using incomplete resolution (overlapping bands) and recycling the mixed fraction (mf) to the feedstock (a) Control of band separation and cut points determines fractional impurities t mij mr and Ami /mr2-<4l)> (b) Chromatogram for separation of pure ds- and trans- 1,3-pentadiene. Components 1, isoprene 2, trans- 1,3-pentadiene 3, cis-l,3-pentadiene 4, cyclo-pentadiene. Component 1 is eluted at almost the same time as component 4 of the...
Gel permeation chromatography Is the method of choice for analysis of thermoplastic resin systems. Corrected for imperfect resolution, chromatogram interpretation yields accurate molecular descriptions, including theoretical, kinetic distributions (, ) The current research is designed to extend the utility of this analytical tool to the analysis of thermoset resins. [Pg.321]


See other pages where Chromatography chromatogram resolution is mentioned: [Pg.170]    [Pg.147]    [Pg.22]    [Pg.668]    [Pg.829]    [Pg.596]    [Pg.19]    [Pg.232]    [Pg.241]    [Pg.23]    [Pg.34]    [Pg.275]    [Pg.147]    [Pg.28]    [Pg.149]    [Pg.290]    [Pg.401]    [Pg.752]    [Pg.974]    [Pg.1011]    [Pg.261]    [Pg.491]    [Pg.551]    [Pg.158]    [Pg.166]    [Pg.418]    [Pg.109]    [Pg.247]    [Pg.53]    [Pg.106]    [Pg.95]    [Pg.32]    [Pg.583]    [Pg.115]    [Pg.69]    [Pg.218]    [Pg.25]   
See also in sourсe #XX -- [ Pg.157 ]




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Chromatography resolution

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