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  • Analytical Chemistry and Spectroscopy  (5)
  • Poly(3-hydroxyalkanoates)  (1)
  • 1
    ISSN: 1572-8900
    Keywords: Poly(3-hydroxyalkanoates) ; cellulose acetate esters ; biodegradation ; activated sludge
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Energy, Environment Protection, Nuclear Power Engineering , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Blends of the bacterially produced polyester poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) with cellulose acetate esters (CAE) further substituted with propionyl or butyryl groups (degree of substitution: 2.60 propionyl and 0.36 acetyl or 2.59 butyryl and 0.36 acetyl, respectively) were exposed for 4 months to activated sludge to determine their biodegradability. Samples of such blends made by solution-mixing and solvent-casting had complex morphologies in which both individual components as well as a miscible blend phase were present. Additionally, the two opposite surfaces of solvent-cast films showed both physical and chemical differences. After 2 months, samples of pure PHBV had degraded by more than 98% (15 mg/cm2 of surface area), whereas a pure CAE sample had degraded less than 1% (〈0.2 mg/cm2). Samples containing 25% CAE lost less than 40% of their initial weights (6 mg/cm2) over the total 4-month period. Samples with 50% CAE lost up to 16% weight (2 mg/cm2), whereas those containing 75% CAE lost only slightly more weight than corresponding sterile control samples (1 mg/cm2). NMR results confirm that weight loss from samples containing 25% CAE resulted only from degradation of PHBV and that the surface of samples became enriched in CAE. Solvent-cast film samples containing equal amounts of PHBV and CAE degraded preferentially on the surface which formed at the polymer-air interface. Scanning electron microscopy and attenuated total reflectance infrared spectroscopy revealed this surface to have a rougher texture and a greater PHBV content.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 18 (1989), S. 851-854 
    ISSN: 0887-6134
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The mass spectrometric behaviour of five structurally different cephalosporins has been studied in detail by means of different ionization/desorption methods (electron impact, fast atom bombardment, desorption chemical ionization, laser-induced vaporization) and metastable ion studies (linked scans and mass-analysed ion kinetic energy spectrometry). The best results were obtained by fast atom bombardment mass spectrometry, leading to both molecular ions and fragment ions diagnostic for structural identification.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Chemical ionization of two 1,4-dihydropyridines, lacidipine and its Z-isomer, and their corresponding pyridines in three different reagent gases and the collision-induced dissociation (CID) of their respective mass-selected protonated molecular ions in the collision energy range 10-200 eV were performed on a multiple quadrupole instrument. The weakness of the Breasted acid NH4+ as a protonating agent is clearly manifested in one of the ammonia positive-ion chemical ionization (CI+) mass spectra which displays the addition ion, [M + NH4]+, as the favoured reaction channel. The stereochemistry of the precursor molecules, the exothermicity of the protonation process and the threshold of certain dissociation channels as a function of the collision energy are among the arguments invoked to explain some of the observed differences between the CI+ mass spectra and the CID data of the different isomers investigated. In an attempt to present a more comprehensive study, some high-performance liquid chromatographic retention times and resolutions are also given.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Rapid Communications in Mass Spectrometry 5 (1991), S. 493-498 
    ISSN: 0951-4198
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: Positive/negative fast-ion bombardment (FIB+/FIB-, negative-ion chemical ionization (CI-) and positive-ion electron ionization (EI+)mass spectrometry are used to investigate a number of 1,4-dihydropyridine derivatives. The FIB+ mass spectra presented, acquired at fixed Cs+ ion-gun voltage as well as at different voltages ranging from 1-16 kV, display a close resemblance to their EI+ mass spectral counterparts. Comparison of the FIB- data with data acquired in ammonia CI- demonstrates that for the type of compound investigated in this work, the latter ionization technique yields a superior molecular anion signal and negligible fragmentation. Some of the FIB+ mass spectra presented display a number of unmistakeable qualitative differences which are tentatively attributed to the isomeric stereo-chemistry of the compounds investigated.
    Additional Material: 6 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 27 (1992), S. 724-729 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Positive fast ion bombardment, positive chemical ionization (CI+) and positive electron impact (EI) ionization mass spectrometry were used to investigate a number of relatively large and structurally related organic molecules. Some of the major dissociation pathways observed in the CH4-CI+ mass spectra are not present under NH3-CI+ conditions, but are obtained in the collision-induced dissociation (CID) spectrum of the 50 eV MH+ molecular ion, formed in the latter reaction. The resemblance between the EI mass spectra and their fast ion bombardment counterparts, the effect of changing the energy of the bombarding Cs+ ion beam over the range 2-16 keV and the different degrees of internal excitation of ions formed in different CI reagent gases are discussed.
    Additional Material: 6 Ill.
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  • 6
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Glucuronic acid conjugates of Lacidipine metabolites were analysed by high-performance liquid chromatog-raphy/mass spectrometry with different ionization techniques, viz. thermospray and chemical ionization with a particle beam interface. Analyses were performed on bile samples collected from dogs after oral administration of 14C-labelled Lacidipine. Phase II metabolites, originating from the conjugation with glucuronic acid of phase I metabolites containing free hydroxy or carboxylic functions, were isolated. Two types of glucuronides, with an ether or an ester bond, were characterized. They showed different mass Spectrometric behaviour owing to a specific interaction with the acetate in the mobile phase.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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