ALBERT

All Library Books, journals and Electronic Records Telegrafenberg

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
  • Chemistry  (11)
  • Polymer and Materials Science  (7)
  • 1H-13C COSY NMR  (1)
  • Chloroplast
  • 1985-1989  (9)
  • 1970-1974  (5)
Collection
Publisher
Years
Year
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Planta 169 (1986), S. 278-288 
    ISSN: 1432-2048
    Keywords: Chloroplast ; Lemna (protein degradation) ; Mitochondrion ; Peroxisome ; Protein deg-radation (size/charge)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Evidence is presented that the organelles of Lemna minor do not degrade as functional units. The proteins of Lemna show wide differences in their rates of degradation and ribulose bisphosphate carboxylase (EC 4.1.1.39) has a particularly slow rate of degradation. Contrary to some earlier evidence, we found no correlation between the rate of soluble-protein degradation and either charge or size of proteins. We could find no correlation between protein degradation and subunit size in any of the organelles of Lemna.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 31 (1986), S. 1655-1662 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Phosphorous, as sodium dihydrogen phosphate, and nitrogen, in the form of a urea-for-maldehyde condensate, were applied to cotton fabric. The flame-retarding character of each treated fabric was assessed by determining the respective limiting oxygen index. Analysis of the results showed that at the lowest levels of applied phosphorous (P = 2%), the presence of nitrogen produced less than an additive combined flame-retarding effect. At higher phosphorous levels, this deviation from additivity increased until at P 〉 6%, the presence of nitrogen antagonized the flame-retarding effect of the phosphorous. These observations are discussed within the current ideas of nitrogen-phosphorous interaction in flame-retardant systems, for cotton-containing fabrics.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 32 (1986), S. 5691-5691 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 169 (1973), S. 177-189 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die elektroinitiierte Polymerisation von N-Vinylcarbazol (VCZ) wurde in Aceton bei 25°C mit Zinkbromid als Katalysator unter Verwendung von Platinelektroden eingehend untersucht. Die Polymerisationsgeschwindigkeit erwies sich als direkt abhängig von der Stromstärke, der Zinkbromid-Konzentration und dem anfänglichen Wassergehalt des Solvens.Die Molekulargewichte der entstandenen Polymeren (1000-6000) sind unabhängig von der Stromstärke, der Zinkbromid-Konzentration und dem Umsetzungsgrad des Monomeren zum Polymeren, werden jedoch beeinflußt durch Wasser, die Monomerkonzentration und das Elektrodenmaterial. Die chemische Zusammensetzung der Polymeren ändert sich nicht mit der Stromstärke, der Zinkbromid-Konzentration, dem Umsetzungsgrad und dem Elektrodenmaterial. Sie ändert sich jedoch ein wenig mit dem Wassergehalt des Acetons.
    Notes: The electroinitiated polymerization of N-vinylcarbazole (VCZ) in acetone solvent at 25°C with zinc bromide, as catalyst, and platinum electrodes was investigated in detail. The polymerization rate was found to be directly dependent on current strength, zinc bromide concentration and the initial water content of the solvent.The molecular weights of the formed polymers (1000-6000) are independent of current strength, zinc bromide concentration and degree of conversion of monomer to polymer, but are affected by water, monomer concentration, and by the type of electrodes used. The chemical composition of the polymer is invariant with current strength, zinc bromide concentration, degree of conversion, and electrode material but does vary slightly with the water content of acetone.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 5
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A gas chromatographic/mass spectormetric assay has been developed for the simultaneous measurement of 2-amino-3,8-dimethylimidazo[4,5-ƒ]quinoxaline (MeIQx) and 2-amino-3,4,8-trimethylimidazo[4,5-ƒ]quinoxaline (DiMeIQx) in fried beef. The method employs capillary column gas chromatography, electron capture negative ion chemical ionization mass spectrometry and a stable isotope labelled analogue of MeIQx as common internal standard. Two patties of lean minced beef which had been cooked separately were analysed and found to contain both compounds (patty 1:2.4 ng MeIQx g-1 meat, 1.2 ng DiMeIQx g-1 meat; patty 2: 1.3 ng MeIQx g-1 meat, 0.5 ng DiMeIQx g-1 meat). Neither compound was present in the meat prior to cooking.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 6
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A gas chromatographic mass spectrometric assay for (N-dicyclopropylmethyl)amino-2-oxazoline in plasma with a detection limit of 0.1 ng ml-1 was required. Various fluoroaryl derivatives of this compound (code name S3341) were synthesized and their positive ion chemical ionization and electron capture negative ion chemical ionization mass spectra recorded. While fluorobenzyl derivatives of S3341 could be made by heating with the requisite benzyl bromide and diisopropylethylamine in acetonitrile, initial efforts to synthesize corresponding fluorobenzoyl derivatives using a benzoyl chloride in dry ethyl acetate at 60 °C were unsuccessful. Mass spectral data indicated that only a fragment of the oxazoline ring was retained in the reaction product and that an N-(2-chloroethyl)benzamide was formed. However, when diisopropylethylamine was included in the reaction mixture, a benzoyl derivative of the complete molecule was obtained. The mechanisms of these reactions are discussed. The negative ion mass spectrum of the 3,5-bistrifluoromethylbenzoyl derivative of S3341 has a base peak at m/z 420 (the molecular ion) and, when this ion is specifically monitored, an amount of derivative equivalent to 1 pg of S3341 can be detected. This allowed the development of an assay for S3341 in plasma with a precision of 9% (SD) at 0.2 ng ml-1 and a lower limit for quantitative determination of 0.1 ng ml-1.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 16 (1972), S. 2449-2459 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The light-induced degradation of aqueous hydroxypropylmethylcellulose (HPMC; D.S. 1.9) solutions has been investigated under a variety of conditions. The HPMC was sensitized to short-wavelength radiation (〈500 nm) by the addition of sodium nitrite, the degradation being accompanied by increased acidity and the generation of oxides of nitrogen. Addition of eosin dye increased the sensitivity to visible light (〉500 nm), and the effect was considerably more pronounced when strong electron donors were added. Analysis of the shear-viscosity relationship of the solutions, during the degradation, indicated that both chain disentanglement and chain scission occurred but that the primary process was the depolymerization of the cellulose chain. It is proposed that both the dye- and nitrite-induced depolymerizations are a consequence of peroxide attack on the β-glucosidic ether link. The results indicate that, in the case of sodium nitrite addition, the peroxide was generated by the aqueous photolytic decomposition of the nitrite ion. The peroxide formation in the eosin - TEA system was a consequence of leuco-dye production, under the influence of the light, followed by the reduction of traces of dissolved oxygen by this activated dye.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Fire and Materials 9 (1985), S. 57-64 
    ISSN: 0308-0501
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Architecture, Civil Engineering, Surveying , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: The use of differential thermal analysis has enabled spontaneous ignition behaviour of cotton cellulose to be investigate. The temperature. Ti, at which the onset of spontaneous ignition occurs is recorded as a function of the oxygen concentration of the flowing oxygen-nitrogen atmosphere to which the cellulose sample is exposed in the DTA furnace, when heated at a defined heating rate. The dependence of Ti, on heating rate has enabled the activation energy, Ep, of the rate-determining flammable pyrolysis product reaction to the determined using both a previously derived simple kinetic model and the technique of Ozawa. Ep, increases from a lower limiting value of 112 kJ mol-1 at zero oxygen concentration to an asymptote value of 169 kJ mol-1 at oxygen volume concentrations above 30%. This effect is described in terms of oxygen catalysis of competing pyrolysis routes. At a given heating rate, increased oxygen concentration reduces Ti. A plot of 1/Ti versus In [O2] gives two liner regions which intersect at an oxygen concentration of about 20%, suggesting that two combustion mechanisms exist, one above and the other below this value. Below this concentration, which is similar to the conventional limiting oxygen for cellulose, significant char remains, suggesting that ignition of gaseous products only occurs. If the difference in slopes is sttributed to the variations in Ep with oxygen concentration, then a value for the activation energy of gaseous product oxidation, Eox = 215 kJ mol-1 is derived.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 9
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 2 (1970), S. 225-226 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 10
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 26 (1988), S. 523-525 
    ISSN: 0749-1581
    Keywords: 1H NMR secondary references ; 13C NMR secondary references ; Temperature dependence ; D2O solutions ; (CD3)2SO solutions ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Chemical shifts of secondary references for D2O and (CD3)2SO solutions were measured as a function of temperature. The 1H and 13C chemical shifts of dioxane, sodium 4,4-dimethyl-4-silapentanesulphonate, HOD, tetramethylammonium chloride and sodium 3-(trimethylsilyl)propionate-d4 in D2O solution were measured relative to external TMS and the chemical shifts of (CD3)2SO and H2O were measured in (CD3)2SO solution relative to internal TMS. For accurate comparison of chemical shifts it is necessary to take into account the sample temperature and, therefore, the temperature dependences of 1H and 13C chemical shifts of a number of secondary references have been determined accurately and fitted to a parabola or straight line, as appropriate.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...