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  • Articles  (3,374)
  • Analytical Chemistry and Spectroscopy  (3,355)
  • 42.75
  • 2000-2004  (120)
  • 1975-1979  (3,254)
  • 1950-1954
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  • Articles  (3,374)
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  • 101
    ISSN: 0935-6304
    Keywords: Clean-up ; aliphatic hydrocarbons ; organochlorine compounds ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: ---No abstract
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  • 102
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 23 (2000), S. 430-436 
    ISSN: 0935-6304
    Keywords: Speciation ; digestion ; capillary electrophoresis ; ferrous ; ferric ; mineral analysis ; complexation ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: ---Capillary electrophoresis is used as a means of cation separation for cationic speciation analysis. Acceptable separation of ferrous and ferric iron was achieved by using a mixed complexing agent run buffer which gave stable species in solution. These iron species, and total iron, were determined simultaneously in certified reference materials with a single digestion step. A variety of digestion techniques were compared, primarily for their non-oxidative capabilities in order to preserve the oxidation state of iron in the mineral samples. The most favorable recoveries resulted from a continuous flow nitrogen purge technique. Total iron levels obtained from the CE method were compared with those determined by two spectroscopic techniques, with similar results obtained using the different instrumental methods.
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  • 103
    ISSN: 0935-6304
    Keywords: Capillary electrophoresis ; UV detection ; organic acids ; background electrolyte optimization ; wine ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: ---A simple technique is described for the routine capillary electrophoretic determination of organic acids in wine samples. Several aromatic and non-aromatic compounds, including phthalic acid, benzoic acid, sorbic acid, boric acid, and phosphate, were evaluated as background electrolytes in order to obtain the highest resolution and detection sensivity. Factors that affect capillary electrophoretic separation such as the concentration and pH of the background electrolyte (BGE), the concentration of the electroosmotic flow modifier (EOF), and methanol addition to the electrolyte were investigated systematically. Tartaric, malic, succinic, acetic, and lactic acids were determined simultaneously in approximately six minutes using an electrolyte containing 3 mM phosphate and 0.5 mM myristyltrimethylammonium bromide (MTAB) as electroosmotic flow modifier at pH 6.5. This method is quantitative, with recoveries in the 90-102% range and linear up to 50 mg L-1. The precision is better than 1% and the procedure shows the appropriate sensibility, with detection limits between 0.015 and 0.054 mg L-1. The proposed method was successfully employed for the determination of organic acids in wine samples by direct sample injection after appropriate dilution and filtration.
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  • 104
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 23 (2000), S. 688-692 
    ISSN: 0935-6304
    Keywords: Solid oxygen scavenger ; carrier gas purity ; manganous oxide ; glass press-fit connections ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: ---No abstract
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  • 105
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 23 (2000), S. 697-698 
    ISSN: 0935-6304
    Keywords: Gentiana rigescens Franch ; gentiopicroside ; swertiamarin ; MEKC ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: No abstract
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  • 106
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 23 (2000), S. 479-484 
    ISSN: 0935-6304
    Keywords: Programmable temperature vaporizing injection (PTV) ; thermal desorption ; gas chromatography ; mass spectrometry ; plasticizers ; polyethylene ; food wrapping film ; explosive powders ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: ---Programmable Temperature Vaporizing Injection (PTV) has been used extensively as a means of injecting large volumes of samples to enhance sensitivity. This paper describes the use of PTV injection in the desorption mode for the analysis of a range of solid samples, and four examples of this application are described in detail. Detection by mass spectrometry was used extensively as a means of identification of the components in the various samples which were characterized.
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  • 107
    ISSN: 0935-6304
    Keywords: High-performance liquid chromatography ; β-methyl amino acids ; enantioseparation ; quinine-derived chiral stationary phase ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A quinine-derived chiral anion-exchange stationary phase was used for the direct high-performance liquid chromatographic separation of the enantiomers of the N-protected unusual β-substituted α-amino acids, β-methylphenylalanine, β-methyltyrosine, β-methyltryptophan, and β-methyl-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid. The readily prepared 2,4-dinitrophenyl and tert-butyloxycarbonyl derivatives were well separated, and in most cases the separation of all four stereoisomers of these β-methyl-α-amino acids could be obtained in one chromatographic run. The elution sequences of the enantiomers of the different derivatives were determined and revealed a dependence on the type of the N-protecting group. In this context, the effects of different protecting groups (acetyl, tert-butyloxycarbonyl, benzoyl, 3,5-dinitrobenzoyl, benzyloxycarbonyl, 3,5-dinitrobenzyloxycarbonyl, 2,4-dinitrophenyl, and 9-fluorenylmethoxycarbonyl) on the chromatographic behavior were investigated.
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  • 108
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 23 (2000), S. 637-643 
    ISSN: 0935-6304
    Keywords: HPLC ; fast separation ; flavan-3-ol ; flavonols ; vegetables ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: ---A fast high-performance liquid chromatography method was used for analysis of prominent flavan-3-ols and flavonols in vegetables. Gradient elution with phosphoric acid-acetonitrile mixtures and phosphoric acid-methanol mixtures allowed fast and complete separation of the studied phenolic compounds within analysis times less than 10 min. The development of two elution gradients using methanol and acetonitrile as modifiers proved to be an excellent approach for the verification of the real polyphenolic composition in vegetables samples because the two optimized methods allowed the separation of the same number of compounds in the same elution order. Diode-array detection was employed for the provisional identification of phenolic compounds that were not available as standards. We preferred methanol as a modifier because it was less toxic and cheaper than acetonitrile. Detection limits ranged between 0.12 and 0.59 μg mL-1. High recoveries of phenolics from fresh vegetables were measured in all studied cases, independent of the phenolic structure, matrix, and vegetable in question. High levels of procyanidins between 150 and 450 mg kg-1 were found in all studied vegetables. Quantification of quercetin and kaempferol glycosides was only possible in marrow and onion, respectively.
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  • 109
    Electronic Resource
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    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 23 (2000), S. 656-658 
    ISSN: 0935-6304
    Keywords: Capillary electrophoresis (CE) ; laser induced fluorescence detection (LIFD) ; fluorescein isothiocyanate (FITC) ; inulin ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: ---No abstract
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  • 110
    ISSN: 0935-6304
    Keywords: Reversed-phase high performance liquid chromatography (RP-HPLC) ; relationships between retention and eluent composition ; linear and quadratic models ; statistical comparison of ; evaluation of HPLC columns ; stationary phases ; lipophilicity/hydrophobicity ; log kw ; log P ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: ---Statistical evaluation of linear and quadratic models of chromatographic retention was performed. The relationships describing retention were derived for a set of 23 carefully selected test analytes chromatographed on 18 HPLC columns using methanol-water or acetonitrile-water solutions as mobile phase. It was ascertained whether the square term in the quadratic model improves the description of chromatographic retention in a statistically significant manner. It was also checked whether the retention data extrapolated to a hypothetical neat water eluent (log kw) obtained with the two models and the two organic modifiers are equivalent or should be considered different. The research proved that both models yield similar results and the extrapolated log kw values do not differ statistically significantly in the case of methanol-containing mobile phases. In the case of acetonitrile-water systems the log kw values obtained with linear and quadratic models are normally statistically different. Correlation analysis for log kw vs. log P parameters was performed for data determined on six columns. The best correlations were achieved employing log kw data derived with the linear model for methanol/water systems.
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  • 111
    ISSN: 0935-6304
    Keywords: High performance size exclusion chromatography ; molecular weight ; lignin derivatives ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: ---No abstract
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  • 112
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 23 (2000), S. 457-473 
    ISSN: 0935-6304
    Keywords: Domestic lignite heating emissions ; isokinetic sampling ; polyaromatic sulfur heterocycles (PASH) ; thiaarenes ; atomic emission detection (AED) ; pulsed flame photometric detection (PFPD) ; high resolution mass spectrometry (HRMS) ; retention indices ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: ---Lignite briquettes with different sulfur contents were burned in a common type of domestic heating system. The levels of polycyclic aromatic sulfur heterocycles (PASH, thiaarenes) and their alkylated and phenylated derivatives in the flue gas were determined. The analytical method described comprises isokinetic sampling, GC/full scan-MS for screening analysis, HPLC/wavelength programmable fluorescence detection (selected PAHs used as internal standards for GC), GC/atomic emission detection or GC/pulsed flame photometric detection (sulfur-selective detection of thiaarenes), GC/high resolution MS (verification and quantification of thiaarenes), and the determination of the gas chromatographic retention indices. In total 57 thiaarene species (individual compounds if possible and groups of isomeric compounds such as alkylated/phenylated species) were identified, their retention indices determined, and quantified as flue gas emission concentrations. Not only thiophene-related thiaarenes but also species with two sulfur atoms in the molecule (e. g. thienothiophene derivatives) were found. The thiaarene emission pattern is discussed, as is the correlation between the thiaarene emissions and the sulfur content of the different briquette types burned.
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  • 113
    Electronic Resource
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    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 23 (2000), S. 489-496 
    ISSN: 0935-6304
    Keywords: Flavor ; odorant ; headspace ; GC ; interaction ; electronic nose ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: ---In order to understand the flavor of foods a multitude of scientific investigations have been carried out and a number of analytical tools for flavor research developed in the last few decades. Initially, scientific investigations focused mainly on the identification of all compounds that could contribute to the flavor. Olfactory GC techniques permitted the division of identified volatiles into odor-active and non-odor-active. Many techniques were developed to enhance the quality and the information content of the flavor results. Since the early 1990s, analytical investigations have dealt with interactions between food matrices and flavor compounds and the human influence on the retardation of odorants. New analytical methods concentrate on the headspace of the sample by using static or dynamic headspace analysis, or deal with measurements of volatile release in the mouth by a novel nose sampler and oral vapor GC. These useful tools clarify the effects of breathing, chewing, and saliva flow on flavor release. Though the human nose performs well at low concentrations of odorants, it is a medium-term aim to replace the use of the human nose by analytical techniques. Future investigations will probably deal with the interactions of odorants and the human receptors and it is mainly these receptors that will play a key role in aroma research. By analysis of the effects of odorants on the receptors the mechanisms of odor perception will be elucidated. This will enable the development of supporting analytical tools like electronic noses that really do function as noses, or “neural networks”.
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  • 114
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    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 23 (2000), S. 519-521 
    ISSN: 0935-6304
    Keywords: Scoparone ; phytoalexin ; citrus ; MEKC ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: ---A new MEKC method has been developed to determine the amount of the phytoalexin, scoparone, in Citrus roots. The separation and analysis was achieved with a running buffer of 100 mM SDS, 25 mM phosphate and 12% (v/v) methanol pH 6.2. Separation was performed at 12 kV with 25°C and UV detection at 200 nm. A near complete recovery of scoparone was obtained with the extraction procedure. The MEKC method was compared with a fluorescence TLC method. The detection limit for scoparone with the MEKC method (2 μg/mL) was better than the TLC method (10 μg/mL).
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  • 115
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    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 23 (2000), S. 215-224 
    ISSN: 0935-6304
    Keywords: Bilinear signal enhancement ; two-dimensional comprehensive gas chromatography ; chemometrics ; GC ; GRAM ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: ---The chemometric method referred to as the generalized rank annihilation method (GRAM) is used to improve the precision, accuracy, and resolution of comprehensive two-dimensional gas chromatography (GC×GC) data. Because GC×GC signals follow a bilinear structure, GC×GC signals can be readily extracted from noise by chemometric techniques such as GRAM. This resulting improvement in signal-to-noise ratio (S/N) and detectability is referred to as bilinear signal enhancement. Here, GRAM uses bilinear signal enhancement on both resolved and unresolved GC×GC peaks that initially have a low S/N in the original GC×GC data. In this work, the chemometric method of GRAM is compared to two traditional peak integration methods for quantifying GC×GC analyte signals. One integration method uses a threshold to determine the signal of a peak of interest. With this integration method only those data points above the limit of detection and within a selected area are integrated to produce the total analyte signal for calibration and quantification. The other integration method evaluated did not employ a threshold, and simply summed all the data points in a selected region to obtain a total analyte signal. Substantial improvements in quantification precision, accuracy, and limit of detection are obtained by using GRAM, as compared to when either peak integration method is applied. In addition, the GRAM results are found to be more accurate than results obtained by peak integration, because GRAM more effectively corrects for the slight baseline offset remaining after the background subtraction of data. In the case of a 2.7-ppm propylbenzene synthetic sample the quantification result with GRAM is 2.6 times more precise and 4.2 times more accurate than the integration method without a threshold, and 18 times more accurate than the integration method with a threshold. The limit of detection for propylbenzene was 0.6 ppm (parts per million by mass) using GRAM, without implementing any sample preconcentration prior to injection. GRAM is also demonstrated as a means to resolve overlapped signals, while enhancing the S/N. Four alkyl benzene signals of low S/N which were not resolved by GC×GC are mathematically resolved and quantified.
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  • 116
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    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 23 (2000), S. 245-252 
    ISSN: 0935-6304
    Keywords: LMCS ; cryogenic modulation ; comprehensive gas chromatography ; GC×GC ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Comprehensive gas chromatography is the realization of true continuous multidimensional (dual column) gas chromatography. The key requirement in the comprehensive GC experiment is that the second dimension analysis is completed in a rapid time-frame compared to the elution of components in the first dimension, and that the two coupled dimensions represent ‘orthogonal’ analyses towards the analytes to be separated. The former normally necessitates pulsing of contiguous segments of each chromatographic band from the first to the second dimensions. The two dimensions should be in fluid communication. The comprehensive GC×GC experiment passes all the column flow from the first column to the second column, leading to no sample loss, but this also requires a suitable method for time- or zone-compression of the band to be pulsed to the second column. The final pulse should be narrow, and should be delivered to the second column quickly. A simple procedure can achieve this using the cryogenic modulator that has been recently described by this group. The system uses a cryogenic trap which can be moved away from the cooled zone of the column faster than 10 ms. A fast-acting pneumatic ram achieves this performance. The cooled column heats up to the prevailing oven temperature within 10-15 ms. Molecules as volatile as C5 alkanes or small aromatics will be fully retained by the trap within the period of modulation used for GC×GC. The technique is simple to implement and requires no special column connections. Using a gas chromatograph which allows control of external events and can acquire from a detector at 50 Hz or faster, and a timing controller for modulation, the comprehensive result can easily and effectively be achieved.
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  • 117
    ISSN: 0935-6304
    Keywords: Retention factors ; styrene divinylbenzene polymer ; porous graphitic carbon ; solid-phase extraction ; water analysis ; polar organic compounds ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: ---LC retention data have been measured using various stationary phases with an emphasis on highly polar to moderately polar neutral organic compounds having octanol-water partition coefficients (Kow) in log units between 0 and 3. The relationships between the retention factor measured in water and the octanol-water partition coefficient are linear but with different slopes for octadecyl (C18) silicas, and two polystyrene divinylbenzene (PS-DVB) phases with low and high surface areas. These relationships confirm that highly cross-linked polymers can provide more than 1000-times higher retention values than C18 silicas for moderately polar analytes but close values for highly polar ones. They also explain why C18 silicas and polymers are equivalent for the separation of very polar analytes. In contrast, due to a different retention mechanism, no relation exists between the retention shown by porous graphitic carbons (PGC) and analyte hydrophobicity, but highly polar analytes are in general much more strongly retained than by any other sorbent. The potential of PGC for both the extraction and the separation of analytes is shown. Due to the difference in separation mechanism, PGC is the analytical phase that should be used for confirmation of the identity of analytes instead of a cyanopropylsilica column as recommended in some environmental procedures. Applications are presented for the trace-determination of triazines and polar degradation products in ground and surface water with detection limits below the 0.1 μg/L level.
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  • 118
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    Journal of High Resolution Chromatography 23 (2000), S. 449-454 
    ISSN: 0935-6304
    Keywords: Denuders ; isolation and enrichment ; analysis ; volatile organic compounds ; partition coefficients Kfs ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: ---The possibility of using a piece of gas chromatographic capillary column as a tubular denuder for isolation and enrichment of organic pollutants present in air was studied. The partition coefficients (Kfs) of typical organic pollutants (benzene, chlorobenzene, toluene) between the gaseous phase and the denuder sorption layer were determined and effects of analyte concentration in the gaseous phase and gas flow rate on partitioning were studied. The partition coefficients were found to be constant in the studied range of concentration and gaseous mixture flow rate. A piece of a capillary column coated with polydimethylosiloxane can be used as a tubular denuder.
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  • 119
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    Journal of High Resolution Chromatography 23 (2000), S. 539-546 
    ISSN: 0935-6304
    Keywords: Headspace sampling ; Headspace Sorptive Extraction (HSSE) ; SPME ; aromatic plants ; medicinal plants ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: ---A new sampling technique, Headspace Sorptive Extraction (HSSE), is here applied for the first time to the headspace sampling of medicinal and aromatic plants. The analyte partition coefficient between HSSE-PDMS stir bar and sample headspace (K1), the concentration factor (CF), the reproducibility, and the minimum recoverable amount were determined by analyzing standard solution of high volatility C5-C7 compounds with different polarities and structures (cyclohexane, propyl acetate, hexanal, 1-hexen-3-ol, isoamyl acetate, and 2-heptanol). Four aromatic and medicinal plants, viz. rosemary (Rosmarinus officinalis L.), sage (Salvia officinalis L.), thyme (Thymus vulgaris L.), and valerian (Valeriana officinalis L.) were analyzed by HSSE-GC with PDMS stir bars, and their concentration capacity was compared with those of S-HS and HS-SPME with different fibers. HSSE showed very high concentration capability with both standard and real sample components.
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  • 120
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    Journal of High Resolution Chromatography 23 (2000), S. 547-553 
    ISSN: 0935-6304
    Keywords: Capillary GC ; static and dynamic headspace sampling ; sorptive and adsorptive extraction ; plant volatiles ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: ---Static and dynamic headspace sampling have been applied for the enrichment of volatiles emitted by living plants. For solid phase microextraction (SPME) the sorptive fibers polydimethylsiloxane (PDMS) and polyacrylate (PA) have been compared and, in accordance with the like-like principle, polar compounds exhibit more affinity for the PA fiber while apolar solutes favor the PDMS fiber. For dynamic sampling, tubes packed with PDMS particles show greater inertness than Tenax; some Tenax decomposition products, e.g. benzaldehyde and acetophenone, interfere with the analyses. With PDMS particles operated in the breakthrough mode, the obtained profiles are similar to those obtained by SPME on the PA fiber. Recoveries relative to a packed PDMS bed are 85% for Tenax, 2.4% for SPME-PDMS, and 6.2% for SPME-PA.
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  • 121
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    Journal of High Resolution Chromatography 2 (1979), S. 74-74 
    ISSN: 0935-6304
    Keywords: Liquid chromatography, HPLC ; Fluocortolon ; Corticoids ; LiChrosorb Si 60/dichlormethan, methanol, water preferable to reversed phase systems ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 122
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    Journal of High Resolution Chromatography 2 (1979), S. 268-269 
    ISSN: 0935-6304
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 123
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    Journal of High Resolution Chromatography 2 (1979) 
    ISSN: 0935-6304
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 124
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    Journal of High Resolution Chromatography 2 (1979), S. 281-281 
    ISSN: 0935-6304
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 125
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    Journal of High Resolution Chromatography 2 (1979), S. 288-292 
    ISSN: 0935-6304
    Keywords: Gas chromatography ; Capillary, glass ; Stationary phases, polar, gum type ; For temperatures up to 300°C ; For most of the common classes of organic compounds ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Most of the common classes of organic compounds chromatograph normally on Superoxes. There is no tailing or adverse effect from excessively different activity different activity coefficients. Superoxes are therefore universal phases for gas chromatography. This is also expressed by a wide useful temperature range from ∼50° to ∼300°. High MW Superox-4 has a MAOT about 20° higher than the lower MW Superox-0.1. Several applications illustrating the versatility of Superox phases in (GC)2 are presented.
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  • 126
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    Journal of High Resolution Chromatography 2 (1979), S. 429-435 
    ISSN: 0935-6304
    Keywords: Gas chromatography ; Capillary, glass ; Surface roughening by diatomaceous support (5 micron particles deposition) ; Organic glue (polar polymethacrylate acetate) used as intermediate material ; Reproducibility and durability of capillaries discussed ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A technique for adhesion of fine particles (ca. 5 μ) of the 405 white diatomaceous support on the inner wall of glass tube with organic glue [poly (diethylaminoethyl methacrylate) acetate] is described. The coated tube was drawn to capillary column by using a machine designed according to Desty's. The capillary column was then coated with stationary phase (such as squaiane, QF-1, Dexsil 300, PEG 20 M, OV-1, SE 30 and etc.) by the conventional dynamic or static method. This preparation method has proved easy to duplicate and is simple. The coating efficiency (UTE %) is within 60-90. The theoretical plate number per meter of an SE 30 column is about 4000, and per meter of a PEG 20 M column is about 2500. The columns thus prepared have been successfully used to analyze petroleum hydrocarbons, essential oils, petrochemicals, pheromone, steroid metabolites and others.
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  • 127
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    Journal of High Resolution Chromatography 2 (1979), S. 585-585 
    ISSN: 0935-6304
    Keywords: High-performance thin-layer chromatography, HPTLC ; Sugar determination by fluorescence ; Detection limit ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 128
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    Journal of High Resolution Chromatography 2 (1979), S. 592-594 
    ISSN: 0935-6304
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
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    Journal of High Resolution Chromatography 2 (1979), S. 591-591 
    ISSN: 0935-6304
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
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    Journal of High Resolution Chromatography 2 (1979), S. 630-631 
    ISSN: 0935-6304
    Keywords: HPTLC ; Liquid scintillation counting ; Specific radioactivity ; Phospholipids ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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    Journal of High Resolution Chromatography 2 (1979), S. 635-636 
    ISSN: 0935-6304
    Keywords: Gas chromatography ; Cyclandelate quantitation ; In plasma. No sylilation needed ; Analysis within 16 min, range 5-50 ng/mikroliter ; Correlation coeff. 0.996 (N=6) ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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    Journal of High Resolution Chromatography 2 (1979), S. 151-153 
    ISSN: 0935-6304
    Keywords: Liquid Chromatography, HPLC ; Stationary phase carrier silicagel analysis and cleaning treatment ; 0.3% metal traces may interfere ; Elution by boiling 1-12 N HCl does not attack C18 bonding in reverse phase material, extracts metals sufficiently ; Effective phase quality test by hop-α-acid chromatogram ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Trace elements in different silica gels are determined by neutron activation analysis. The presence of 20 elements in the ppm range and of 15 elements in the ppb range is established in all silica gels; even in spherical material probably obtained via an organosilicium starting material. Removal of these elements by acid treatment before and after derivatization to a reversed-phase is studied. This is only partially effective. The resulting HPLC phases are, however, much better in cases where trace elements are detrimental. Even octadecyl derivatized silicagel can withstand boiling in 12 N hydrochloric acid without loosing significant amounts of bonded organic material.
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    Journal of High Resolution Chromatography 2 (1979), S. 156-159 
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    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
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    Journal of High Resolution Chromatography 2 (1979), S. 155-155 
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    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
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    Journal of High Resolution Chromatography 2 (1979) 
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    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
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  • 136
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    Journal of High Resolution Chromatography 2 (1979), S. 172-176 
    ISSN: 0935-6304
    Keywords: Chromatography, LC and GC ; Capillary ; Theory ; Ultimate resolution ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The expression for the resolution function, R, in terms of operating parameters for open tubular columns has been extended to include inlet contributions to the peak variance. Subsequent optimization has revealed the existence of optima in the column radius, the stationary phase thickness and the diffusion coefficient ratio in the stationary and mobile phases-in addition to the well-known optimum in the flow velocity. This implies that R at optimum becomes R=f(K)L0.6Vi-0.2, i.e. a function only of the column length, L, the inlet volume, Vi, and the concentration distribution coefficient, K. For given K, L and Vi all other parameters such as retention time and pressure drop can thus be directly computed. The information is finally consolidated in the form of contour diagrams. The text itself is cast in the form of a science fantasy.
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    Journal of High Resolution Chromatography 2 (1979), S. 177-183 
    ISSN: 0935-6304
    Keywords: Gas chromatography ; Capillary ; Injection by tailored capsule-insertion technique ; Critical comparison with split-injection technique ; Competitive with best-known systems ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A capsule-insertion system tailored to the needs of capillary gas chromatography is described. It provides the basis for a truly quantitative and improved qualitative approach to open tubular capillary GLC. The advantages of the system lie in its simplicity of handling and in the possibility of using relatively low injection temperatures, thus reducing the risks to thermally unstable samples.The observed high efficiencies characterizing this capillary GLC capsule technique allow full advantage to be taken of the operating capacity of the superior capillary columns to give a performance competitive with the best known split-injection systems.
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    Journal of High Resolution Chromatography 2 (1979), S. 211-215 
    ISSN: 0935-6304
    Keywords: Liquid chromatography, HPLC ; Reverse phase separation of 9 antibiotics ; Down to 5 min analysis time, less than 4% repeat variation ; Precise analytical conditions given ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Chromatographic methods are presented for the determination of chloramphenicol, erythromycin, tyrothricin, nystatin, penicillin, streptomycin, sulphanilamides and nitrofurans, in some pharmaceutical formulations. The methods have been applied in routine analysis and are in general capable of distinguishing the main antibiotic from decomposition products and likely congeners.
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    Journal of High Resolution Chromatography 2 (1979), S. 254-254 
    ISSN: 0935-6304
    Keywords: Gas chromatography ; Hydrodesulphurization products elution ; Room temperature two-column operation ; Chemistry ; Analytical Chemistry and Spectroscopy
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    Journal of High Resolution Chromatography 2 (1979), S. 255-256 
    ISSN: 0935-6304
    Keywords: Liquid Chromatography, HPLC ; Peptide analysis ; Angiotensin I and II, peptide hormones, resolution of impurities ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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    Journal of High Resolution Chromatography 2 (1979), S. 263-266 
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    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
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    Journal of High Resolution Chromatography 2 (1979), S. 268-268 
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    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
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    Journal of High Resolution Chromatography 2 (1979), S. 282-282 
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    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
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    Journal of High Resolution Chromatography 2 (1979), S. 283-287 
    ISSN: 0935-6304
    Keywords: Gas chromatography ; Capillary, glass ; Sampling technique ; Semi-automation of head space sampling ; Application to water pollution, coffee aroma, light hydrocarbons in crude oil ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Head space GC using a special electropneumatic sampling system works well in combination with glass capillaries. Because a homogenous gas mixture is already present most problems inherent with inlet splitters are thus avoided. In cases where the high vapor pressure of the sample can cause problems with the pressure controlled sampling system, the use of narrow bore glass capillaries provides the necessary inlet pressure. The use of this powerful and convenient analytical tool for water pollution analysis, flavour analysis and the analysis of volatiles in crude oil samples is shown by examples.
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    Journal of High Resolution Chromatography 2 (1979), S. 319-323 
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    Keywords: Gas chromatography ; Capillary, glass ; Mobile phase flow programming ; Comparison with temperature programming ; Short capillaries offer considerable shorter analysis time when flow programmed ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The technique of programming the carrier gas flow rate in gas chromatography, especially in connection with the use of capillary columns shorter than 10 m can significantly accelerate GC analyses. Equations for calculation of the parameters of the exponential flow function and retention data are described. The effects of flow programming in a short capillary column are shown in a few chromatograms. Different programming rates are tested and compared with temperature programming.
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    Journal of High Resolution Chromatography 2 (1979), S. 297-302 
    ISSN: 0935-6304
    Keywords: Gas chromatography ; Capillary, glass ; Surface roughening ; Amorphous silica ; Deactivation ; Column performance ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A new method for the preparation of wall-coated glass capillary columns after surface roughening by means of amorphous silica is described. After the glass capillary has been leached, a small quantity of amorphous silica is deposited evenly on the inner surface. This is done by passing a plug of dilute water glass through the capillary, followed by a flow of gaseous hydrochloric acid. The roughened surface is stabilized, deactivated and finally coated.This paper furnishes details of the technique and information about the performance of a number of columns prepared by the method.
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    Journal of High Resolution Chromatography 2 (1979), S. 324-328 
    ISSN: 0935-6304
    Keywords: Gas chromatography ; Capillary, glass ; Theory in contrast to traditional approaches ; Very practical formulas for peak width, maximum load, concentration in mobile phase ; Optimizing procedure for trace analysis ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In contrast to traditional theoretical approaches by calculation of (nonexistent) theoretical plates, a unified theory of gas chromatography as given by a definition of the resolution analogue to methods in signal processing or spectroscopy using the well-known Kovacz indices as fundamental scale. A derivation of the thusly defined resolution from basic physical principles yields very practical formulae for peak width, maximum load, substance flow in peak maximum, concentration of substance in the carrier gas and other interesting parameters in dependence of capillary diameter, capillary length, film thickness, carrier gas speed, viscosities etc. Diagrams show favourite conditions for detectors responding on absolute substance flow (e.g. FID) or on concentrations.
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    Journal of High Resolution Chromatography 2 (1979), S. 392-392 
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    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
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    Journal of High Resolution Chromatography 2 (1979), S. 400-404 
    ISSN: 0935-6304
    Keywords: Gas chromatography ; Capillary, glass ; Low temperature plasma etching ; Polymer film on the inner surface from organosilicone monomer ; Flexibility of this new method discussed ; Discharge chamber described ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A novel method is described for the preparation of stable glass capillary columns (glass open tubular columns), including the etching and formation of a polymer film on the inner glass capillary surfaces. The approach used here is based on low-temperature plasma etching and polymerization. Under the influence of a field of radio frequency discharge, low pressure gases of fluoric compounds, introduced into the glass capillary tube, generate excited fluorine radicals which etch the inner surface. The plasma of organosilicone monomer in the glass capillary yields a uniform polymerized film on the inner surface. The resultant material functions as a good stationary phase for glass capillary gas chromatography (GC2). The inner surfaces treated with such a plasma, can be studied by means of a scanning electron microscope (SEM). The flexibility of this method permits the use of various stationary phases and surface modification.
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    Journal of High Resolution Chromatography 2 (1979), S. 416-422 
    ISSN: 0935-6304
    Keywords: Gas chromatography ; Capillary, glass ; SECAT-technique=stepless fine tuning of capillary selectivity by serial column temperature optimization ; Exponential influence of temperature on selectivity over a wide range found ; SECAT-technique ready for automation of column adjustment on sample composition polarity ; Instrumental and methodological details for primitive self made solution given ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: GC, including capillary GC, is rather inflexible, if a certain column length and stationary phase has been fixed for a given analytical problem. If the sample composition changes, one often has to change the column length and/or stationary phase, at least when something like optimum analytical conditions are needed. Temperature changes (or heating rates) can change the selectivity of a given column only within very limited ranges, due to the exponential effect of temperature on retention time. By serial coupling two chemically different capillaries, each run at another temperature, even the slightest changes of these two temperature values have a dramatic effect on the selectivity of the system for polar substances. We call this technique the SECAT mode of GC. Results are reported as retention index shifts, dependent on SECAT temperature data. This technique can in future easily be automated, thus enabling the analyst, for polar sample analysis, to adjust a given chroma-tographic system to his specific sample composition without touching the instrument.
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    Journal of High Resolution Chromatography 2 (1979), S. 393-394 
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    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
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    Journal of High Resolution Chromatography 2 (1979), S. 389-391 
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    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
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    Journal of High Resolution Chromatography 2 (1979), S. 487-496 
    ISSN: 0935-6304
    Keywords: Gas chromatography ; Capillary, glass ; Comparison of FID, ECD, FPD for detection limit. linearity, peak shape etc. ; Practical results for pesticide residue and coal hydrogenation products given ; Concentration dependent detectors in capillary GC interesting, when optimized ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A comparison of the characteristics and Performance of the flame ionization, electron capture, and flame photometric detectors with capillary columns is described. Factors which may affect the limits of detection, linearity, chromatographic peak shape, and other detector performance characteristics are discussed and compared with the results of a model derived for the behavior of concentration and mass flow-rate dependent chromatographic detectors used with capillary GC systems. Examples are given of highly complex and labile mixtures such as pesticide residues and products from coal hydrogenation.
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    Journal of High Resolution Chromatography 2 (1979), S. 500-506 
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    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
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    Journal of High Resolution Chromatography 2 (1979), S. 581-582 
    ISSN: 0935-6304
    Keywords: Gas chromatography ; Retention indices and substituent constants ; Phenols ; Polar stationary phases ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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    Journal of High Resolution Chromatography 2 (1979), S. 586-586 
    ISSN: 0935-6304
    Keywords: Thin-layer chromatography, TLC ; Direct application of amniotic fluid without extraction ; Lecithin/Sphingomyelin ratio measured, precision approxi-mately 5% ; Procedure faster, simpler, requires less amniotic fluid ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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    Journal of High Resolution Chromatography 2 (1979), S. 621-622 
    ISSN: 0935-6304
    Keywords: Uroporphyrin isomer separation ; HPLC uroporphyrin free acid ; Uroporphyrin isomers in urine ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A synthetic mixture of uroporphyrin isomers I, II, III and IV as free acids in the synthetic ratio of 1:1:4:2 was resolved by reverse-phase HPLC using a C0:PEL (ODS) 37-50 micron precolumn and a Micro Bondapak C18 analytical column eluted with acetonitrile (4%) in phosphate buffer (pH 6.95). Clinically important I and III isomers of uroporphyrin were readily resolved directly from acidified urine as porphyrin free acids.
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    Journal of High Resolution Chromatography 2 (1979), S. 617-620 
    ISSN: 0935-6304
    Keywords: High-performance liquid chromatography ; Ion pairing ; Reversed-phase ; Catecholamines, epinephrine ; Mammalian uterus ; Boronate affinity gel column chromatography ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Catecholamine standards have been separated by ion pairing reversed-phase high-performance liquid chromatography (HPLC). A trace substance was separable from four standards when low concentrations of methanol were used in the elution buffer. This method has allowed separation of an unknown uterine catecholamine, partially purified on a boronate affinity gel column, from the standards: norepinephrine, epinephrine, normetanephrine and metanephrine.
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    Journal of High Resolution Chromatography 2 (1979), S. 632-632 
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    Keywords: Sample preparation ; Modification of standard purging device ; Simpler sample introduction and vessel clean up ; Minimization of loss of volatiles in ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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    Journal of High Resolution Chromatography 2 (1979), S. 633-634 
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    Keywords: Liquid chromatography ; Ion exchange ; Diaminostilbenedisulfonic acids ; Chemistry ; Analytical Chemistry and Spectroscopy
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    Topics: Chemistry and Pharmacology
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    Journal of High Resolution Chromatography 2 (1979), S. 647-653 
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    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
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    Topics: Chemistry and Pharmacology
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    Journal of High Resolution Chromatography 2 (1979), S. 669-670 
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    Keywords: High performance thin-layer chromatography ; Unsaturated fatty acids ; p-Hydroxybenzaldehyde ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A rapid method for the detection and quantltatlve determlnation of unsaturated fatty acids by TLC is presented. After separation on HPTLC-RP18-plates, reaction wlth p-hydroxybenzaldehyde is carried out by a dipping procedure. Nanogram amounts of unsaturated fatty acids can be determined with good reproducibility.
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  • 163
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    Keywords: Gas chromatography ; Capillary, glass ; Surface deactivation, persllylation ; Discussion of variable parameters ; Suggested practical procedure ; Chemistry ; Analytical Chemistry and Spectroscopy
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    Journal of High Resolution Chromatography 2 (1979), S. 628-628 
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    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
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    Journal of High Resolution Chromatography 2 (1979), S. 629-630 
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    Keywords: Gas chromatography ; Capillary glass ; Nitrogen-specific detection ; TMSN ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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    Journal of High Resolution Chromatography 2 (1979), S. 637-640 
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    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
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    Topics: Chemistry and Pharmacology
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    Journal of High Resolution Chromatography 2 (1979), S. 642-644 
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    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
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    Journal of High Resolution Chromatography 2 (1979), S. 605-608 
    ISSN: 0935-6304
    Keywords: Addition of variances and second moments in chromato-graphy, GC, LC ; Additivity of homogeneous column contributions ; Additivity of extra-column contributions ; Estimation of time constant from peak shape ; Discontinuous plate number ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The time constant, τ, is determined from the tail of an authentic HPLC peak through a plot of In U versus time, t, according to the relation \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm In\, U} = {\rm In }\mathop {\rm U}\nolimits_{\rm o} - \frac{1}{\tau }{\rm \,t} $$\end{document} expected at low recorder deflexions, U. The value obtained, τ = 2.43 s, is one order of magnitude larger than an ordinary recorder time constant, which is quite normal for LC detectors. It agrees with the value, τ = 2.44 s, needed theoretically to distort a Gaussian-shaped peak so as to obtain the experiment-ally found second moment, σ2 = 11.13 s,2 and the experimental difference between first moment t and peak retention time tmax, t - tmax = 0.78 s. The determination is therefore regarded as a demonstration of the variance addition rule \documentclass{article}\pagestyle{empty}\begin{document}$$ \sigma ^2 = \sigma \frac{{\rm 2}}{{\rm G}} + \tau ^2 $$\end{document} where σG2 is the second moment of the non-distorted peak. The column contribution version \documentclass{article}\pagestyle{empty}\begin{document}$$ (\sigma ')^2 = \sigma \frac{2}{{\rm o}}_{{\rm (k)}} + \sigma \frac{{\rm 2}}{{\rm s}} $$\end{document} is also considered. This equation was appliied earlier to an estimation of extra-column contributions to band broadening with the aid of the “abt” concept. An explicitly k-(capacity ratio)-dependent expression for the mass exchange contribution, σG2 is derived from Golay's equation for capillary columns, but the validity of the Golay equation is under discussion.
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    Journal of High Resolution Chromatography 2 (1979), S. 743-745 
    ISSN: 0935-6304
    Keywords: Liquid chromatography, HPLC ; Molecular exclusion technique ; Protein separation ; Peptides up to 50,000 daltons separated ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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    Journal of High Resolution Chromatography 2 (1979), S. 752-754 
    ISSN: 0935-6304
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
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  • 171
    ISSN: 0935-6304
    Keywords: Gas Chromatography ; Thermodynamic properties measured, interaction energy vapour polymers ; Precise Vgº-data measured ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The interaction energies (X1) between the polymers polypropylene, poly(vinylidene chloride), sulphonyldiphenyl formaldehyde resin and poly(vinyl pyrrolidone) and the solvents toluene, ethylbenzene, isopropylbenzene, ortho, meta, and para-xylene are determined by gas chromatography. As shown in earlier publications, this technique for the determination of X1, can be extended to similar systems of theoretical as well as of practical importance, although the selection of the present systems was primarly made on the fact that these systems are of industrial interest and have not so far been investigated by gas-liquid chromatography. The studies were carried out at two temperatures and the results obtained show a decrease of X1 with an increase of temperature.
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  • 172
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    Journal of High Resolution Chromatography 2 (1979), S. 31-35 
    ISSN: 0935-6304
    Keywords: Gas chromatography ; Capillary, glass ; Surface deactivation, silylation ; Inertia stable to 350° ; Free acids and bases, simultaneous injection ; On-column injection ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A deactivation procedure is described based on a published method using hexamethyldisilazane in the gas phase. In addition to unusually high inertia and thermostability, the method produces truly neutral columns which allow simultaneous analysis of moderately strong free acids and bases. The silylated columns show their full potential only with on-column injection. Preliminary experimental directions are given; more elaborate directions will become available after extended optimization work.
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  • 173
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    Journal of High Resolution Chromatography 2 (1979), S. 36-38 
    ISSN: 0935-6304
    Keywords: Thin-Layer Chromatography, TLC, HPTLC ; Error analysis for quantitation chromatographic and sampling error often largest ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The paper describes the measurement and calculation of the primary statistical errors in the evaluation of TLC or HPTLC using in situ reflectance measurements. The primary errors are the errors of the sample volume spotted onto the plate, errors caused by the chromatographic process itself, the positioning error of the plate with respect to the centre of the light beam and the error in the light measurement. By scanning the same spot, the same track or the same plate under different conditions, the various errors can be determined.
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  • 174
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    Journal of High Resolution Chromatography 2 (1979), S. 529-530 
    ISSN: 0935-6304
    Keywords: Gas chromatography ; Requirements with respect to pressure controllers ; Design of pressure controllers ; All-metal controllers ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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    Journal of High Resolution Chromatography 2 (1979) 
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    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
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  • 176
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    Journal of High Resolution Chromatography 2 (1979), S. 95-100 
    ISSN: 0935-6304
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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    Journal of High Resolution Chromatography 2 (1979), S. 91-92 
    ISSN: 0935-6304
    Keywords: Data evaluation, peak width measurements in GC, LC, TLC ; Peaks are in principle non symmetric, non Gaussian shaped ; Standard deviation and variance cannot be measured directly as usual ; Systematic error easily larger than 50% ; Calculation of correct standard deviation/variance presented ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 178
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    Journal of High Resolution Chromatography 2 (1979), S. 93-94 
    ISSN: 0935-6304
    Keywords: Chromatography Theory peak shape, mathematical basis of real standard deviation and variances are much larger than “measured” ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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    Journal of High Resolution Chromatography 2 (1979), S. 101-101 
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    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
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    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
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    Journal of High Resolution Chromatography 2 (1979), S. 102-102 
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    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
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    Journal of High Resolution Chromatography 2 (1979), S. 108-108 
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    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
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  • 183
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    Journal of High Resolution Chromatography 2 (1979), S. 118-122 
    ISSN: 0935-6304
    Keywords: Liquid Chromatography, HPLC ; Cannabis extract, 11 constituents separated ; Quantitation by electrochemical detector ; Δ9 Tetrahydrocannabinol down to 2-20 ng ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A simple, isocratic high performance liquid chromatography system (HPLC) with electrochemical detection (EC) was used to study Cannabis constituents. Several Cannabis extracts and reference standards were examined. A total of eleven constituents were separated, and three major cannabinoids; Δ8, Δ9 tetrahydrocannabinol (THC) and cannabidiol (CBD) were identified. A linear relationship was established for the quantitation of the halucinogenic constituent Δ9 THC. Minor contaminants in Δ9 THC reference standard, which were not detected by gas chromatography (GC) were detected for the first time. The detection limits of Δ9 THC and related cannabinoids were in the low nanogram range (2-20 ng).
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  • 184
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    Journal of High Resolution Chromatography 2 (1979), S. 109-117 
    ISSN: 0935-6304
    Keywords: Gas Chromatography, capillary, glass ; Capillary versus packed column ; Small sample width at inlet important ; Optimized sampling by on-column injection ; Hydrogen as ideal carrier gas ; Efficient and stringent testing of columns needed ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Capillary gc is now rapidly expanding. Naturally, initiation is most often attempted on the basis of the experience acquired with packed columns. However, such an extrapolation is successful only if a number of essential peculiarities of capillary gc are considered. Based on practical examples this paper discusses six essential details: 1) design and maintenance of the gas flow paths, 2) the greatly increased importance of sampling technique, which should not be confined just to stream splitting, 3) the problems in quantitative analysis arising from small sample size, 4) specific sources of trouble related to small amounts of liquid phase, 5) specific arguments for the choice of the carrier gas, clearly pointing to hydrogen as the ideal carrier and, 6) the different way to approach column production. Figures for all selected examples are given.
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    Journal of High Resolution Chromatography 2 (1979), S. 123-132 
    ISSN: 0935-6304
    Keywords: Gas Chromatography, preparative capillary ; Injection, automatic ; Separation is two dimensional ; Trapping of total effluent ; Splitter pneumatically controlled, variable ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The present paper describes an automated system for preparative gas chromatography with glass capillary columns, controlled by a microprocessor. The effluent from the capillary column is divided by a pneumatically controlled splitter and any desired split ratio between traps and detector can be obtained. Moreover, a second pneumatic control allows instantaneous change-over to a different split ratio, thus minimizing loss of material during collection.The effluent containing the compounds of interest is passed through a multiple manifold and collected in coiled glass capillary traps. To ensure maximum trapping efficiency even for very small amounts of material, the inner walls of the capillary traps are wetted with a suitable solvent, which gives a quantitative recovery of micro- and nanogram amounts of material.After repetitive sampling, sufficient amounts of material can be obtained for NMR spectroscopy and possibilities exist to enrich trace components with the aid of a double column system. Two examples of such applications are given, employing mixtures of both synthetic and natural origin.
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    Journal of High Resolution Chromatography 2 (1979), S. 703-711 
    ISSN: 0935-6304
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 187
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    Journal of High Resolution Chromatography 2 (1979), S. 720-722 
    ISSN: 0935-6304
    Keywords: Chromatography, theory ; Peak width as a function of retention time and capacity ratio “abt” concept ; Real plate height and theoretical plate height Extra-column contributions to band broadening and “abt” concept ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Kaiser's “abt” concept rests on the experimental establishment of a linear relation between band width at half height, b0.5, and capacity ratio, k, according to \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm b}_{{\rm 0}{\rm .5}} = {\rm b}_{\rm o} + {\rm ak} $$\end{document} His column specification quantity, hreal, is dependent on the square of the slope a, obtained from a linear regression analysis based on this relation. It is shown in the present paper that an improvement of the experimental conditions leading to a lower extra-column contribution to band broadening, bex2, introduces a tendency towards a negative curvature in the plot at low k values. The mean slope increases, and an uncritical linear regression would yield an hreal-value which is higher than before and which would be in the opposite direction to the requirements of a reliable column specification. Generally the linear regression analysis has to be moved to higher k regions in cases of curvature, especially as it is also shown that hreal is an estimation of the traditional HETP value, H∞, that would be obtained when k approaches infinity. This theoretically expected relation \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm h}_{{\rm real}} = {\rm H}_\infty $$\end{document} is a strong motivation for the use of hreal as a column specification, since the b0.5-value associated with H∞ is expected to be practically independent of bex2.
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    Journal of High Resolution Chromatography 2 (1979), S. 147-148 
    ISSN: 0935-6304
    Keywords: Chromatography GC, LC ; Extra-column contribution ; Band broadening ; Plate concepts, real plate number; theoretical plate number; discontinuous plate number ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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    Journal of High Resolution Chromatography 2 (1979), S. 141-144 
    ISSN: 0935-6304
    Keywords: Liquid Chromatography, HPLC ; Anthelmintic drug analysis, rapid quantitation by internal standard technique ; Mebendazole, ciclobendazole ; Drug Assay ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A procedure for determining the anthelmintic drug mebendazole in plasma of patients is described. Mebendazole together with the internal standard ciclobendazole is extracted with chloroform at pH 11. The extract is analyzed isocratically on a LiChrosorb SI 60 column with a mobile phase consisting of acetonitrile/water-saturated chloroform/ammonia (75/92.5/0.1) at 307 nm. Reproducibility with a coefficient of variation of 3 to 10% is attainable for the concentration range of 20 to 200 ng mebendazole/ml plasma. Mebendazole plasma concentrations in patients with echinococcosis on chronic therapy with mebendazole ranged from 6 to 117 ng/ml.
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    Journal of High Resolution Chromatography 2 (1979), S. 154-154 
    ISSN: 0935-6304
    Keywords: Liquid Chromatography, HPLC, ion-exchange ; Specific detection of alkaloids ; Post-column derivatization - fluorimetric ion-pair technique ; Fluorimetric determination of tropane alkaloids in pharmaceuticals ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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    Journal of High Resolution Chromatography 2 (1979), S. 149-150 
    ISSN: 0935-6304
    Keywords: Liquid Chromatography, HPLC ; Ion pair reverse phase gradient technique starting at low pH ; Viral associated glycosoaminoglycans, G2 and G4 separated ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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    Journal of High Resolution Chromatography 2 (1979), S. 186-186 
    ISSN: 0935-6304
    Keywords: Gas chromatography ; Carrier gas ; Flow control by flattened tube restriction ; Fine tuning by adjustable twisting ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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    Journal of High Resolution Chromatography 2 (1979), S. 184-184 
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    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
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    Journal of High Resolution Chromatography 2 (1979), S. 187-188 
    ISSN: 0935-6304
    Keywords: Gas chromatography ; Capillary, glass ; Whiskers, OV-17 ; Steroid profiling ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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    Journal of High Resolution Chromatography 2 (1979), S. 164-171 
    ISSN: 0935-6304
    Keywords: Liquid chromatography, gradient technique ; Mobile phase composition programming by hardware construction ; Effluent composition curve analysis ; Numerical method for calculation and theory discussed ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The theory of gradient elution under hydrostatic equilibrium is developed for the case where only one reservoir and one mixing chamber are used and where both solvents have equal densities. Given the shapes of the two vessels, effluent concentration curve equations are deduced for different mixing chamber-reservoir combinations. On the other hand, given the equation for the effluent concentration curve, the reservoir cross-sectional area, as a function of height, can be deduced when the mixing chamber has a constant cross-section. The varying cross-section of the reservoir is accomplished by inserting thin discs of different areas on top of one another inside a regular vessel of constant cross-section.Except for complicated gradients, a given gradient can be accomplished using a reservoir with a cross-sectional area which varies linearly with height. In the case of complex gradients, a reservoir having two or more linear segments becomes necessary. A numerical method is given for the calculation of the continuously varying reservoir cross-section for the exact duplication of a given gradient.
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    Journal of High Resolution Chromatography 2 (1979), S. 189-190 
    ISSN: 0935-6304
    Keywords: Gas Chromatography ; Capillary, glass ; Tin-selective FPD ; Triphenyltin hydroxide ; TPTH ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A new method for the determination of triphenyltin hydroxide using capillary column gas chromatography with a tin-selective flame photometric detector has been developed. Triphenyltin hydroxide and its potential metabolites are converted to methyl derivatives and separated on glass capillary columns coated with OV-101. Derivatization of triphenyltin hydroxide, triphenyltin chloride, diphenyltin dichloride, phenyltin trichloride, and bis-triphenyltin oxide is nearly quantitative with a minimum of redistribution products. The selectivity of the flame photometric detector is cearly demonstrated by the comparison of chromatographic profiles obtained from using both the flame photometric and flame ionization detectors.The use of this chromatographic system in the analysis of triphenyltin hydroxide in a fortified water sample demonstrates the potential use of this system in organotin residue chemistry.
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    Journal of High Resolution Chromatography 2 (1979), S. 191-192 
    ISSN: 0935-6304
    Keywords: Chromatography, theory ; Extra-column Contribution ; Band broadening “abt” concept ; Taylor equation ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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    Journal of High Resolution Chromatography 2 (1979), S. 229-235 
    ISSN: 0935-6304
    Keywords: Thin-layer chromatography, TLC ; Separation of Zn, Cu, Al, Ga, In as oxinates ; Styragel 60A and Merckogel OR-PVA 2000 layers used ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Gel chromatographic behavior of 8-hydroxyquinoline (oxine, abbreviated HOx) complexes of zinc, copper, aluminum, gallium and indium has been investigated on thin layers of Styragel 60A and Merckogel OR-PVA 2000 mostly in chloroform and p-dioxan media. Except for the stable Cu(Ox)2, the other oxinates exhibit either hydration or decomposition in gel-solvent-solute systems, which leads to strong retention or tailing on gel layers. An excess of 8-hydroxyquinoline present in solvents allows the oxinates to be stabilized, so that well-defined compact spots come out and migrate. For the Zn(Ox)2 the formation of a self-adduct is strongly suggested on the basis of gel chromatographic behavior. Elution with the solvent containing pyridine also yields evidence of the adduct formation of zinc oxinate-nitrogen base.
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    Journal of High Resolution Chromatography 2 (1979), S. 243-245 
    ISSN: 0935-6304
    Keywords: Gas Chromatography, instrumentation ; Detectors with dual ionization cells, ECD, FID ; Applications in packed and capillary GC ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In order to avoid splitting at the column outlet for simultaneous multidetection, a new line of detector heads with the ionization cells coupled in series has been developed.The electron capture plus flame ionization detector (EC+FI-D) has been evaluated from the point of view of the sensitivity, the linear dynamic range and separation efficiency in a capillary column GC system. The performances of each section are the same as when a single ionization detector head is used.
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    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
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    Topics: Chemistry and Pharmacology
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