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  • 11
    Electronic Resource
    Electronic Resource
    Trace enrichment of polar pollutants from water and the influence of humic substances (1993)
    Springer
    Chromatographia 37 (1993), S. 13-19 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Polar pollutants in water ; On-line trace enrichment ; Humic substances
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A practical liquid chromatographic early-warning system for polar pollutants in water ought to have detection limits at a level below a microgram per litre. Using ultraviolet absorbance detection this normally necessitates trace enrichment of the samples. In this study ten different sorbents have been tested with respect to their enrichment capacity. The hydrophobic polymeric PLRP-S material, in combination with a C-18 modified analytical column, proved to be the best choice. The influence of humic substances, present in surface water, was also studied. Lowering of the sample pH, resulted in a significant increase in the interferences due to the humic substances.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02272181
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  • 12
    Electronic Resource
    Electronic Resource
    Use of membrane extraction disks for on-line trace enrichment of organic compounds from aqueous samples (1990)
    Springer
    Chromatographia 29 (1990), S. 415-418 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Trace enrichment ; Membrane extraction disks ; Triazine herbicides ; 2,3,4-Trichlorophenol
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Membrane extraction disks have been recently introduced for the solid-phase extraction of organic compounds from aqueous samples. The material consists of alkyl-modified silica particles enmeshed in an inert PTEE matrix. Aqueous samples containing polar pesticides and herbicides, are preconcentrated on-line from acidic solutions on membrane extraction disks containing immobilized octadecyl-modified silica and analyzed with an isocratic liquid chromatographic system using PLRP-S as the stationary phase and aqueous acetonitrile mixtures (pH 3) as the eluent. Data on the lifetime and the dimensions of the preconcentration disks, and the efficiency and the repeatability of the procedure are reported. For 10 ml samples, the detection limits of the analytes atrazine, simazine and 2,3,4-trichlorophenol in tap water are 0.1–1 ppb.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02261387
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  • 13
    Electronic Resource
    Electronic Resource
    Immunoaffinity precolumn for selective sample pretreatment in column liquid chromatography: Immunoselective desorption (1991)
    Springer
    Chromatographia 31 (1991), S. 469-477 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Immunoaffinity precolomn ; Oestrogens ; Bioanalysis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary An automated liquid chromatographic system is described using immunoaffinity precolumns for sample pretreatment. The system consists of a column-switching unit allowing preconcentration from a large volume of sample (e.g. 15 ml of urine) onto an immunoaffinity precolumn (containing polyclonal antibodies immobilized on Sepharose). After sorption, the analytes are desorbed by a mixture of two cross-reacting solutes, followed by reconcentration on a C-18-bonded silica precolumn, and then separation on a C-18-bonded silica analytical column. Using oestrogen steroids as model compounds and UV absorbance detection, the minimum detectable concentration is ca. 200 ng/l with a repeatability of 6–8%. The total analysis time is 45 min which allows the unattended analysis of 30 samples per day. The features of the sample pretreatment method, especially of the immunoselective desorption, are evaluated and the general applicability of the system is discussed.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02262391
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  • 14
    Electronic Resource
    Electronic Resource
    Determination of polar pollutants in water using an on-line liquid chromatographic preconcentration system (1991)
    Springer
    Chromatographia 32 (1991), S. 445-452 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; On-line preconcentration ; Polar pollutants ; Water (tap and surface)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary An isocratic column liquid chromatographic system with UV absorbance detection at 230 nm has been developed for the rapid trace-level determination of a large number of polar pollutants in water. The systems contains two precolumns, in series, which are packed with a styrenedivinylbenzene (PLRP-S) polymer. The second precolumn is also loaded with sodium dodecylsulphate before use. Each precolumn is combined with a PLRP-S analytical column, and aqueous acetonitrile mixtures (pH 3) are used for the separation of neutral as well as acidic and basic pollutants. With 10-ml water samples the detection limits for all analytes, in tap water, are in the low to sub μg/l range. Relevant analytical data are reported and the advantage of using a dodecylsulphate-loaded precolumn over a cation-exchange precolumn is discussed.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02327976
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  • 15
    Electronic Resource
    Electronic Resource
    Optimization of enantiomeric separations with chiral bonded phases (1986)
    Springer
    Chromatographia 21 (1986), S. 205-213 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Chiral phases ; Optimization of separation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The preparation and properties of chiral bonded phases with amino acid groups are described. These phases were used in non-polar eluents and in aqueous systems in the presence of Cu2+ ions in the ligand-exchange mode. The optimization of chiral resolution is demonstrated for both cases. With non-polar eluents similarity between bonded groups and solutes is required. The elution could be accelerated by non-protonic moderators. Ligand-exchange separation is influenced by the copper content of the eluent and the stationary phase, the organic moderator concentration, the pH and ionic strength of the buffer and by the temperature. Structural requirements of both the bonded groups and of the solutes for chiral separation are discussed.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02311888
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  • 16
    Electronic Resource
    Electronic Resource
    On-line post-column extraction in column liquid chromatography with electron-capture detection (1986)
    Springer
    Chromatographia 22 (1986), S. 235-240 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Reversed-phase system ; On-line post-column extraction ; Electron-capture detection
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A post-column extraction module has been used for the on-line coupling of conventional-size (4.6mm i.d.) reversed-phase liquid chromatography (PPLC) and electron-capture detection (ECD). Hexane and toluene were used as extraction solvents, while methanol turned out to be preferable to dioxane and acetonitrile as modifier in the aqueous eluent. In this system the ECD behaves as a concentration-sensitive detector. The band broadening in the evaporation interface, which connects the extraction module with the ECD, dominates the total post-column band broadening; it can be reduced to 3–4 sec by directing at least 0.25–0.30 ml/min (i.e. 25–30%) of the extraction solvent to the ECD. Optimal signal-to-noise ratios were observed if 30–60% of the extraction solvent is directed to the ECD. The noise levels are 5–10 times higher than in systems using a direct coupling of normal-phase LC or narrow-bore reversed-phase liquid chromatography to the ECD. Separations of phenylurea herbicides and chlorophenols demonstrate the applicability of the RPLC-extraction module-ECD system.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02268765
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  • 17
    Electronic Resource
    Electronic Resource
    An expert system for the optimization of columns, operating conditions and instrumentation for high-pressure liquid chromatography (1988)
    Springer
    Chromatographia 26 (1988), S. 37-44 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Expert systems ; Optimization of operating parameters
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Given the mobile and the stationary phase and values for the physical parameters such as temperature and pH, a separation can be optimized by varying the so-calledchromatographic parameters. These include the column dimensions, particle size, operating conditions (e.g. flow rate, attenuation) and instrumentation (e.g. detector cell, time constant). Optimization of the chromatographic parameters implies finding the best possible set of values, which we define as yielding (i) sufficient separation and (ii) sufficient sensitivity in (iii) the shortest possible time. Finding the best possible conditions (the global optimum) is very difficult for chromatographers in practice. An expert system is described that allows chromatographic optimization to be performed for isocratic separations. An initial chromatogram is required to consult the system. In return, the system provides a complete set of chromatographic parameters, which represents the global optimum within the limits set by the required resolution and signal-to-noise ratio specified by the user. The tolerated flow and pressure ranges, the volume of the available detector cells and the time constant of the detection system are constraints during the optimization. A separate module of the system concerns the sample preparation for pharmaceutical formulations in solid dosages and aqueous solutions. Prototype expert systems have been successfully implemented in the expert-system shell Knowledge Craft on a MicroVAX workstation.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02268122
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  • 18
    Electronic Resource
    Electronic Resource
    On-line procedures for the phase-transfer-catalyzed dansylation of phenolic steroids — Application to biological samples (1988)
    Springer
    Chromatographia 26 (1988), S. 267-273 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Phase-transfer catalysis ; On-line derivatization ; Phenolic steroids
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Commercially available equipment from two manufacturers served to set up an automated system for the precolumn phase-transfer-catalyzed dansylation of phenolic steroids, using ethynyl estradiol (EE) and estradiol (E) as model compounds. Using different mixing techniques, the on-line determination of EE and E in 200μl untreated urine samples was achieved at a rate of 3–8 analyses per hour. Detection limits were calculated to be 3–5 ng/ml. Calibration curves in urine were linear over two orders of magnitude with r=0.999 (n=5) for EE and r=0.999 (n=6) for E. The repeatability of the determination of EE in urine (1μg/ml) was 3.9% (RSD; n=20) and of E (1.5μl/ml) 3.8% (RDS; n=10). The use of plasma instead of urine in the on-line procedures was not possible due to rapid formation of emulsions, but E and EE were determined in 100μl plasma samples using a mild off-line mixing procedure in 10min. Detection limits were calculated to be ca 10ng/ml. A reaction detector, based on a solvent-segmented system, was developed for the on-line post-column dansylation of phenols and was coupled with a reversed-phase LC system. The highly selective system showed excellent linearity over at least two orders of magnitude with r=0.9999 (n=6) for both phenol and 2,5-dimethylphenol. The reproducibility was good with RSD values of around 2%. Detection limits for loop injections from standard solutions were calculated to be between 4 and 11ng.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02268165
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  • 19
    Electronic Resource
    Electronic Resource
    Measurement of elastin hydrolysis by reverse-phase HPLC with on-line post-colum derivatization (1989)
    Springer
    Chromatographia 27 (1989), S. 225-227 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Reverse-phase chromatography ; Elastin Hydrolysis measurement ; On-line post-column derivatization
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Excessive breakdown of elastin, a structural protein, may be related to aortic disease and emphysema. Since L-valyl-L-proline occurs in high concentrations in elastin, a rapid and sensitive method using HPLC with post-column on-line derivatization was used to measure the dipeptide from swine aortic tissue, and the amount of elastin present was determined. Elastin was extracted by alkaline hydrolysis. After neutralization and filtration, the sample was injected onto a ODS-2 gel column, and the dipeptide was eluted by a linear gradient of 0 to 10% of 1-propanol in 50 mM heptafluorobutyrate, pH 3, at a flow rate of 1 ml/min. The eluent was reacted with fluorescamine at pH 8.6, and fluorescence was detected at an excitation wavelength of 395 nm and a 455 nm cutoff emission filter.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02260451
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  • 20
    Electronic Resource
    Electronic Resource
    Liquid chromatography — Particle beam mass spectrometry for identification of unknown pollutants in water (1993)
    Springer
    Chromatographia 37 (1993), S. 159-167 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Particle beam interface-mass spectrometry ; Water analysis and identification of unknown ; pollutants ; Phenylurea herbicides
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Trace enrichment on a precolumn packed with copolymer material, coupled on-line with reversed-phase, column liquid chromatography-particle beammass spectrometry (RPLC-PB-MS) has been used for both target and non-target analysis of water samples. RPLC is carried out on a C-18-bonded silica column using a linear acetonitrile-0.1 M ammonium acetate gradient. Using optimised PB-MS conditions and 100–250 ml water samples, the detection limits for several phenylureas are in the 0.03–0.05 μg l−1 range using the full-scan mode; repeatability is good and the LC-PB-MS system is robust. Several surface and drinking water samples have been analysed and low levels of various environmental contaminants have been identified using electron impact mass spectra. Applying chemical ionisation with methane as reagent gas in both the positive and negative mode in conjunction with PB-MS provides relevant confirmatory information.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02275854
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