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  • Analytical Chemistry and Spectroscopy  (23)
  • Barium  (11)
  • Wiley-Blackwell  (34)
  • 1990-1994  (32)
  • 1970-1974  (2)
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Year
  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 13 (1990), S. 759-763 
    ISSN: 0935-6304
    Keywords: Thermal degradation ; N-methylcarbamate pesticides ; PTV injection ; On-column injection ; Splitless injection ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: An experiment has been designed to study the thermal degradation of thermolabile compounds caused by various injection techniques. The four carbamate pesticides aminocarb, bendiocarb, carbaryl, and dioxacarb decompose thermally into methylisocyanate and the corresponding phenol. The carbamets and the phenols arising from them were separated on a 25 m SE-54 fused silica column; all compounds exhibited sharp peak shape indicating that the degradation observed took place completely within the injector.When cold on-column injection was employed no thermal degradation was observed whereas with hot splitless injection at 220°C decomposition of the carbamates was almost complete.PTV injection was found to produce intermediate results. When packed with glass wool and operated with glass wool and operated with starting temperatures lower than the boiling point of the solvent, decomposition was found to be almost complete. Applying isothermal conditions at 140°C (30°C above the boiling point of toluene) aminocarb and bendiocarb underwent only slight decomposition while carbaryl and dioxacarb were about half degraded. Results from PTV injection with an empty insert resembled those obtained using cold on-column injection and in this mode the application of temperatures up to 200°C resulted in no visible degradation. This can be explained by the short residence time of the sample in the injector.
    Additional Material: 4 Ill.
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  • 2
    ISSN: 0935-6304
    Keywords: Capillary gas chromatography ; Split injection ; Bacterial FAME analysis ; 3-OH FAME ; Aldehyde formation ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 13 (1990), S. 697-701 
    ISSN: 0935-6304
    Keywords: Capillary GC ; Injection techniques ; Deterioration by biological matrix ; Thermolabile compounds ; Pesticide analysis ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: An experiment was designed to study the long-term stability of analyses of pesticide residues in a complex food matrix using three different injection techniques. A spinach sample was spiked with five sulfur-containing pesticides of varying volatility and thermolability: azinphos-ethyl, dimethoate, methiocarb, ethiofencarb, and tri-allate. Tri-allate was selected as internal standard because of its thermal stability and its good chromatographic properties. Flame photometric detection resulted in chromatograms not subject to interference by peaks of compounds of the matrix. Starting with a clean and freshly, silanized injector an additional deactivation was found to occur on the first injection of a food sample resulting in an increased peak area for all pesticides in relation to tri-allate. Highest long-term stability was found with PTV injection. Best results for thermolabile carbamates were obtained using on-column injection. However, they were prone to faster deterioration.
    Additional Material: 2 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 14 (1991), S. 174-177 
    ISSN: 0935-6304
    Keywords: Open tubular liquid chromatography ; Ion chromatography ; Potentiometric microelectrode ; Silanes as stationary phases in LC ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Fused silica columns of 4.6 μm i.d. were coated with 3-sulfopropylsilane as a cation exchanger and 3-(2-aminoethyl-amino)-propylsilane as an anion exchanger. Fast separations of cations (〈 25 seconds) and of anions (〈 35 seconds) were obtained, using a potentiometric microelectrode as a detector. In proceeding towards smaller i.d.s, a mixture of alkali metal cations could be separated successfully in an uncoated fused silica capillary of 2.3 μm i.d. as a result of retention by the surface silanol groups at pH 9.4.
    Additional Material: 5 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 19 (1990), S. 390-392 
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
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  • 6
    ISSN: 0951-4198
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: Two congeners Q4 and Q5 inferred in earlier analyses to be cyclic succinimide-type dehydration product; of recombinant hirudin (variant 1) were structurally fully characterized. After isotopic labeling by ring-opening with H218O, the suspected anhydro-positions Asp53 and Asp33 were confirmed by tandem mass spectrometry (MS/MS) sequencing of relevant smaller peplides directly in the enzymatic hydrolysates (V8 protease) using electrospray MS/MS. The chosen strategy proved highly efficient and sensitive.
    Additional Material: 6 Ill.
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  • 7
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Mass spectrometric analysis of the recombinant hybrid plasminogen activator K2tu-PA at the native glycoprotein and corresponding protein level (high mass) is described. For gross structural characterization of the major glycotypes present, a combination of enzymatic degradation and matrix-assisted laser desorption mass spectrometric analysis of the products proved convenient. In this way, mono- and di-N-glycosylated one- and two-chain molecules, unresolved in the spectra of native material, were identified, with the one-chain type monoglycosylated at Asn247 representing the major component. Actual detection of resolved original glycoforms, or unresolved groups thereof when composed of isobaric species, and their assignments regarding antennicity and degree of sialylation were possible by electrospray mass spectrometry for the major monoglycosylated one-chain species. Desialation also allowed detection of the diglycosylated one-chain species as a minor constituent. The electrospray mass spectrometric results were correlated with structural and quantitative data available from a parallel high-performance liquid chromatographic and 1H nuclear magnetic resonance study performed at the glycan (low mass) level on liberated individual carbohydrate components. The results of the two studies showed full consistency in all respects amenable to evaluation, i.e. excellent agreement for the assignments of antennicity and degree of sialylation of the major glycan components, and good agreement for the determination of proportions in which these were present in the major monoglycosylated glycoprotein. This provided a sound basis for direct glycoform profiling by electrospray mass spectrometry. Typical applications to batch quality control and to structural characterization of nonstandard material are shown.
    Additional Material: 6 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 13 (1990), S. 34-39 
    ISSN: 0935-6304
    Keywords: Capillary gas chromatography ; Cold trapping ; Sampling in stainless steel canisters ; Calibration ; Halocarbons in remote areas ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 5 ml air samples from 1.6 l stainless steel canisters were cryogenically preconcentrated before gas chromatographic separation on a thick-film capillary using a home-made cryotrap. Quantification in the 10-500 ppt range was carried out with an electron capture detector. Problems during the cryotrap step were caused by carrier gas contamination, water and CO2 content of the sample, and a non-optimal heat desorption rate. Their elimination is described in detail. Compound losses by wall adsorption on stainless steel surfaces were observed when dry gases were used for standard generation. A static multipoint calibration technique using humidified He was developed allowing a precise standard generation down to 100 ppt. The concentration changes in the stainless steel canisters could be neglected over a storage period of at least 1 month as long as a sufficient degree of humidity was present. The overall reproducibility of the quantification and calibration technique is in the order of 1-2% for concentrations between 100-400 ppt when daily recalibrations are carried out.
    Additional Material: 4 Ill.
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  • 9
    ISSN: 0935-6304
    Keywords: Capillary GC ; Mycobacterium ; Single colony ; Trimethylsulfonium hydroxide (TMSH) ; Fatty acid methyl esters (FAMEs) ; Mycolic acid cleavage products (MACPs) ; Secondary alcohols ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Trimethylsulfonium hydroxide (TMSH) reproducibly converts fatty acids bound in, e.g., biomolecules such as phospholipids and/or glycerides, into the corresponding fatty acid methyl esters (FAMEs). The transesterification can be performed at room temperature in a fast single step reaction. Surprisingly, secondary alcohols and mycolic acid cleavage products (MACPs) are also released from mycobacteria under these conditions.The complex reaction mixtures containing FAMEs, MACPs, and secondary alcohols can easily be separated by high resolution temperature-programmed capillary GC. Different species of mycobacteria give rise to characteristic chromatographic patterns and the amount of lipids from a single colony of mycobacteria is sufficient for reliable identification of the bacteria. The profiles of the chromatograms match well those obtained from other sample preparation techniques.The TMSH method of identification of mycobacteria from the patterns of the gas chromatograms is faster and more sensitive than conventional methods, which also involve transesterification. The identification of mycobacterial species by microbiological culture techniques is difficult to perform and requires several weeks.
    Additional Material: 5 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 29 (1994), S. 713-719 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Various derivatives of a set of three isomeric (linear and branched) pentasaccharides (LNF-1, LNF-2 and LNF-3) were prepared and investigated by high-performance tandem mass spectrometry in order to compare their collision-induced dissociation (CID) behaviour. The fast atom bombardment tandem mass spectra of [M + H]+ ions of peracetylated derivatives mainly display fragments containing the non-reducing terminus (B-type ions) and allow a straightforward assignment of sugar sequence and branching together with the identification of some interglycosidic linkages. Permethylated derivatives, which better accommodate the mass range of tandem mass spectrometers in the case of larger oligosaccharides, yield similar results, i.e. predominance of B ions, but the necessary information has to be retrieved from incomplete Bi and Yi ion series. By contrast, CID of permethyl or peracetyl derivatives carrying a preformed charge due to prior reductive amination of the oligosaccharides with trimethyl(p-aminophenyl)ammonium chloride yields exclusively fragment ions comprising the reducing end. In this case, the four distinct series of fragments observed involve charge-remote fragmentation processes. As a consequence, the spectral patterns are not significantly affected by the nature of the sugar O-substituents additionally introduced (i.e. methyl or acetyl).
    Additional Material: 4 Ill.
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