Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

High Resolution Chromatography

P. Miller (Ed.), High Resolution Chromatography A Practical Approach, Oxford University Press, Oxford, 1999. ISBN 0199636486. [Pg.46]

Figure 2.6 Gas cluotnatograni of a 10 ml test sample containing C I4 C26 alkanes in -hexane (about 1 ppb each) the earner gas (H2) inlet pressure was 2.5 bar for a 22 m X 0.32 mm id separation column coupled with a 2 m X 0.32 mm id uncoated precolumn (no vapour exit). Reprinted from Journal of High Resolution Chromatography, 9, K. Grob et al., Concunent solvent evaporation for on-line coupled HPLC-HRGC , pp. 95-101, 1986, with peimission from Wiley-VCH. Figure 2.6 Gas cluotnatograni of a 10 ml test sample containing C I4 C26 alkanes in -hexane (about 1 ppb each) the earner gas (H2) inlet pressure was 2.5 bar for a 22 m X 0.32 mm id separation column coupled with a 2 m X 0.32 mm id uncoated precolumn (no vapour exit). Reprinted from Journal of High Resolution Chromatography, 9, K. Grob et al., Concunent solvent evaporation for on-line coupled HPLC-HRGC , pp. 95-101, 1986, with peimission from Wiley-VCH.
Figure 2.7 Gas clnomatogram obtained for 500 jl1 of diluted gasoline in -pentane inti O-duced by concunent eluent evaporation, using w-heptane as the co-solvent. Reprinted from Journal of High Resolution Chromatography, 11, K. Grob and E. Muller, Co-solvent effects for preventing broadening or loss of early eluted peaks when using concunent eluent evaporation in capillary GC. Part 2 w-heptane in w-pentane as an example , pp. 560-565, 1988, with permission from Wiley-VCH. Figure 2.7 Gas clnomatogram obtained for 500 jl1 of diluted gasoline in -pentane inti O-duced by concunent eluent evaporation, using w-heptane as the co-solvent. Reprinted from Journal of High Resolution Chromatography, 11, K. Grob and E. Muller, Co-solvent effects for preventing broadening or loss of early eluted peaks when using concunent eluent evaporation in capillary GC. Part 2 w-heptane in w-pentane as an example , pp. 560-565, 1988, with permission from Wiley-VCH.
Figure 2.19 Schematic representation of an on-line liquid-liquid extraction-GC/AED system. Reprinted from Journal of High Resolution Chromatography, 18, E. C. Goosens et al, Continuous liquid-liquid extraction combined on-line with capillary gas chromatography- atomic emission detection for environmental analysis , pp. 38-44, 1995, with permission from Wiley-VCH. Figure 2.19 Schematic representation of an on-line liquid-liquid extraction-GC/AED system. Reprinted from Journal of High Resolution Chromatography, 18, E. C. Goosens et al, Continuous liquid-liquid extraction combined on-line with capillary gas chromatography- atomic emission detection for environmental analysis , pp. 38-44, 1995, with permission from Wiley-VCH.
Figure 2.20 Schematic representation of the set-up used for on-line exti action-GC VI and V2, valves PI and P2, syringe pumps L, sample loop CC flow, countercunent flow CT, cold ti ap. Reprinted from Journal of High Resolution Chromatography, 16, H. G. J. Mol et ai, Use of open-tubular tapping columns for on-line exti action-capillary gas cluomatography of aqueous samples , pp. 413-418, 1993, with permission from Wiley-VCH. Figure 2.20 Schematic representation of the set-up used for on-line exti action-GC VI and V2, valves PI and P2, syringe pumps L, sample loop CC flow, countercunent flow CT, cold ti ap. Reprinted from Journal of High Resolution Chromatography, 16, H. G. J. Mol et ai, Use of open-tubular tapping columns for on-line exti action-capillary gas cluomatography of aqueous samples , pp. 413-418, 1993, with permission from Wiley-VCH.
Figure 10.1 Analysis of racemic 2,5-dimethyl-4-hydroxy-3[2H]-furanone (1) obtained from a strawbeny tea, flavoured with the synthetic racemate of 1 (natural component), using an MDGC procedure (a) dichloromethane extract of the flavoured strawbeny tea, analysed on a Carbowax 20M pre-column (60 m, 0.32 mm i.d., 0.25 p.m film thickness earner gas H2, 1.95 bar 170 °C isothermal) (b) chirospecific analysis of (1) from the sti awbeny tea exti act, ti ansfened foi stereoanalysis by using a pemiethylated /3-cyclodextrin column (47 m X 0.23 mm i.d. canier gas H2, 1.70 bar 110 °C isothemial). Reprinted from Journal of High Resolution Chromatography, 13, A. Mosandl et al., Stereoisomeric flavor compounds. XLIV enantioselective analysis of some important flavor molecules , pp. 660-662, 1990, with permission from Wiley-VCH. Figure 10.1 Analysis of racemic 2,5-dimethyl-4-hydroxy-3[2H]-furanone (1) obtained from a strawbeny tea, flavoured with the synthetic racemate of 1 (natural component), using an MDGC procedure (a) dichloromethane extract of the flavoured strawbeny tea, analysed on a Carbowax 20M pre-column (60 m, 0.32 mm i.d., 0.25 p.m film thickness earner gas H2, 1.95 bar 170 °C isothermal) (b) chirospecific analysis of (1) from the sti awbeny tea exti act, ti ansfened foi stereoanalysis by using a pemiethylated /3-cyclodextrin column (47 m X 0.23 mm i.d. canier gas H2, 1.70 bar 110 °C isothemial). Reprinted from Journal of High Resolution Chromatography, 13, A. Mosandl et al., Stereoisomeric flavor compounds. XLIV enantioselective analysis of some important flavor molecules , pp. 660-662, 1990, with permission from Wiley-VCH.
Figure 10.2 MDGC-MS differentiation between the enantiomers of theaspiranes in an aglycone fraction from puiple passion fruit DB5 pre-column (25 m X 0.25 mm i.d., 0.25 p.m film thickness canier gas He, 0.66 ml/min oven temperature, 60-300 °C at 10 °C/min with a final hold of 25 min) permethylated /3-cyclodextrin column (25 m X 0.25 mm i.d., 0.25 p.m film thickness canier gas He, 1.96 ml/min 80 °C isothermal for 20 min and then programmed to 220 °C at 2 °C/min). Reprinted from Journal of High Resolution Chromatography, 16, G. Full et al., MDGC- MS a powerful tool for enantioselective flavor analysis , pp. 642-644, 1993, with permission from Wiley-VCH. Figure 10.2 MDGC-MS differentiation between the enantiomers of theaspiranes in an aglycone fraction from puiple passion fruit DB5 pre-column (25 m X 0.25 mm i.d., 0.25 p.m film thickness canier gas He, 0.66 ml/min oven temperature, 60-300 °C at 10 °C/min with a final hold of 25 min) permethylated /3-cyclodextrin column (25 m X 0.25 mm i.d., 0.25 p.m film thickness canier gas He, 1.96 ml/min 80 °C isothermal for 20 min and then programmed to 220 °C at 2 °C/min). Reprinted from Journal of High Resolution Chromatography, 16, G. Full et al., MDGC- MS a powerful tool for enantioselective flavor analysis , pp. 642-644, 1993, with permission from Wiley-VCH.
Figure 10.4 Schematic representation of the multidimensional GC-IRMS system developed by Nitz et al. (27) PRl and PR2, pressure regulators SV1-SV4, solenoid valves NV— and NV-I-, needle valves FID1-FID3, flame-ionization detectors. Reprinted from Journal of High Resolution Chromatography, 15, S. Nitz et al, Multidimensional gas cliro-matography-isotope ratio mass specti ometiy, (MDGC-IRMS). Pait A system description and teclinical requirements , pp. 387-391, 1992, with permission from Wiley-VCFI. Figure 10.4 Schematic representation of the multidimensional GC-IRMS system developed by Nitz et al. (27) PRl and PR2, pressure regulators SV1-SV4, solenoid valves NV— and NV-I-, needle valves FID1-FID3, flame-ionization detectors. Reprinted from Journal of High Resolution Chromatography, 15, S. Nitz et al, Multidimensional gas cliro-matography-isotope ratio mass specti ometiy, (MDGC-IRMS). Pait A system description and teclinical requirements , pp. 387-391, 1992, with permission from Wiley-VCFI.
Reprinted from Journal of High Resolution Chromatography, 15, S. Nitz et ah, Multidimensional gas chi omatography-isotype ratio mass spectrometry (MDGC-IRMS). Part A system description and technical requirements, pp. 387-391, 1992, with peraiission from Wiley-VCH. [Pg.228]

Figure 10.13 GC clrromatogram obtained after on-line LC-GC(ECD) of a human milk sample analysed for PCBs (attenuation X 64). Peak identification is as follows (1) PCB 28 (2) PCB 118 (3) PCB 153 (4) PCB 138 (5) PCB 180 (6) PCB 170 (7) PCB 207. Reprinted from Journal of High Resolution Chromatography, 20, G. R. van der Hoff et al, Determination of organochlorine compounds in fatty matiices application of normal-phase LC clean-up coupled on-line to GC/ECD , pp. 222-226, 1997, with permission from Wiley-VCH. Figure 10.13 GC clrromatogram obtained after on-line LC-GC(ECD) of a human milk sample analysed for PCBs (attenuation X 64). Peak identification is as follows (1) PCB 28 (2) PCB 118 (3) PCB 153 (4) PCB 138 (5) PCB 180 (6) PCB 170 (7) PCB 207. Reprinted from Journal of High Resolution Chromatography, 20, G. R. van der Hoff et al, Determination of organochlorine compounds in fatty matiices application of normal-phase LC clean-up coupled on-line to GC/ECD , pp. 222-226, 1997, 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 12.20 SFC-GC analysis of a sample of aviation fuel (a) SFC separation into two peaks (b and c) coixesponding GC ttaces of the respective peaks (flame-ionization detection used throughout). Reprinted from Journal of High Resolution Chromatography, 10, J. M. Levy et ah, On-line multidimensional supercritical fluid chromatography/capillary gas chromatography , pp. 337-341, 1987, with permission from Wiley-VCH. Figure 12.20 SFC-GC analysis of a sample of aviation fuel (a) SFC separation into two peaks (b and c) coixesponding GC ttaces of the respective peaks (flame-ionization detection used throughout). Reprinted from Journal of High Resolution Chromatography, 10, J. M. Levy et ah, On-line multidimensional supercritical fluid chromatography/capillary gas chromatography , pp. 337-341, 1987, with permission from Wiley-VCH.
Figure 13.1 Monitor (FID) (a) and analytical (ECD) (b) channel responses for PCB congeners in Aroclor 1254, showing selection of the six heart-cut events Frr-st columns, HT8 second columns, BPX5. Reprinted from Journal of High Resolution Chromatography, 19, R. M. Kinghorn et al., Multidimensional capillar-y gas chr omatography of polychlorinated biphenyl marker compounds , pp. 622-626, 1996, with per-mission from Wiley-VCH. Figure 13.1 Monitor (FID) (a) and analytical (ECD) (b) channel responses for PCB congeners in Aroclor 1254, showing selection of the six heart-cut events Frr-st columns, HT8 second columns, BPX5. Reprinted from Journal of High Resolution Chromatography, 19, R. M. Kinghorn et al., Multidimensional capillar-y gas chr omatography of polychlorinated biphenyl marker compounds , pp. 622-626, 1996, with per-mission from Wiley-VCH.
Figure 15.1 Separation of pesticides from butter by using LC-GC-ECD. Peak identification is as follows 1, HCB 2, lindane 5, aldrin 7, o,p -DDE 10, endrin 11, o,p -DDT 13, p,p -DDT peaks 3, 4, 6, 8, 9, 12, 14, 15 and 16 were not identified. Adapted from Journal of High Resolution Chromatography, 13, R. Barcarolo, Coupled EC-GC a new method for the on-line analysis of organchlorine pesticide residues in fat , pp. 465-469, 1990, with permission from Wiley-VCH. Figure 15.1 Separation of pesticides from butter by using LC-GC-ECD. Peak identification is as follows 1, HCB 2, lindane 5, aldrin 7, o,p -DDE 10, endrin 11, o,p -DDT 13, p,p -DDT peaks 3, 4, 6, 8, 9, 12, 14, 15 and 16 were not identified. Adapted from Journal of High Resolution Chromatography, 13, R. Barcarolo, Coupled EC-GC a new method for the on-line analysis of organchlorine pesticide residues in fat , pp. 465-469, 1990, with permission from Wiley-VCH.
Figure 15.11 (a) Total ion clnomatogram of a Grob test mixture obtained on an Rtx-1701 column, and (b) re-injection of the entire clnomatogram on to an Rtx-5 column. Peak identification is as follows a, 2,3-butanediol b, decane c, undecane d, 1-octanol e, nonanal f, 2,6-dimethylphenol g, 2-ethylhexanoic acid h, 2,6-dimethylaniline i, decanoic acid methyl ester ], dicyclohexylamine k, undecanoic acid, methyl ester 1, dodecanoic acid, methyl ester. Adapted from Journal of High Resolution Chromatography, 21, M. J. Tomlinson and C. L. Wilkins, Evaluation of a semi-automated multidimensional gas chromatography-infrared-mass specti ometry system for initant analysis , pp. 347-354, 1998, with permission from Wiley-VCH. [Pg.424]

Figure 15.14 Separation of explosives exnacted from water by using SPE-SFE-GC at several SEE trapping temperatures, peak identification is as follows NG, nitroglycerin 2,6-DNT, 2,6-dinitrotoluene 2,4-DNT, 2,4-dinitrotoluene TNT, triniti otoluene IS, 1,3-tiichloroben-zene. Adapted Journal of High Resolution Chromatography, 16, G. C. Slack et al., Coupled solid phase extraction supercritical fluid extraction-on-line gas cliromatography of explosives from water , pp. 473-478, 1993, with permission from Wiley-VCH. Figure 15.14 Separation of explosives exnacted from water by using SPE-SFE-GC at several SEE trapping temperatures, peak identification is as follows NG, nitroglycerin 2,6-DNT, 2,6-dinitrotoluene 2,4-DNT, 2,4-dinitrotoluene TNT, triniti otoluene IS, 1,3-tiichloroben-zene. Adapted Journal of High Resolution Chromatography, 16, G. C. Slack et al., Coupled solid phase extraction supercritical fluid extraction-on-line gas cliromatography of explosives from water , pp. 473-478, 1993, with permission from Wiley-VCH.
The samples of PM-2 and PM-3 probably consist of at least 3 kinds of isomers with the same molecular formula according to high-resolution chromatography. [Pg.286]

Noroozian E, Maris FA, Nielen MWF, et al. 1987. Liquid chromatographic trace enrichment with on-line capillary gas chromatography for the determination of organic pollutants in aqueous samples. Journal of High Resolution Chromatography and Chromatography Communications 10 17-24. [Pg.308]

Cleanup, fractionation and concentration prior to high-resolution chromatography... [Pg.440]

Figure 7.18 Schematic diagram of an SFE-cSFC-HRMS/FID system. After Biicherl et al. [431]. From T. Biicherl et al., Journal of High Resolution Chromatography, 17, 765-769 (1994). Wiley-VCH, 1994. Reproduced by permission of Wiley-VCH... Figure 7.18 Schematic diagram of an SFE-cSFC-HRMS/FID system. After Biicherl et al. [431]. From T. Biicherl et al., Journal of High Resolution Chromatography, 17, 765-769 (1994). Wiley-VCH, 1994. 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. 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.
Hanai, T., Tran, C., Hubert, J. (1981) An approach to the prediction of retention times in liquid chromatography../. High Resolution Chromatography Chromatography Communication (J. HRC CC) 4, 454—460. [Pg.906]

High-resolution chromatography normally yields a protein that is 98-99 per cent pure. The next phase of downstream processing entails formulation into final product format. This generally involves ... [Pg.159]

See other pages where High Resolution Chromatography is mentioned: [Pg.43]    [Pg.548]    [Pg.502]    [Pg.23]    [Pg.32]    [Pg.34]    [Pg.39]    [Pg.59]    [Pg.227]    [Pg.239]    [Pg.275]    [Pg.410]    [Pg.156]    [Pg.394]    [Pg.651]    [Pg.407]    [Pg.310]    [Pg.84]   
See also in sourсe #XX -- [ Pg.232 ]



SEARCH



Chromatography resolution

© 2024 chempedia.info