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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim [u.a.] : Wiley-Blackwell
    Materials and Corrosion/Werkstoffe und Korrosion 35 (1984), S. 401-406 
    ISSN: 0947-5117
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Description / Table of Contents: Hydrolysis of o-dichlorobenzene-water-mixtures In neutral to acid conditions and its importance when selecting materials of constructionWater-saturated o-dichlorobenzene and o-dichlorobenzene-watermixtures were investigated for hydrolysis under neutral and acid conditions and the exclusion of light. Some measurements were also taken in presence of iron oxides and also metallic iron.Chloride ion generation grows with increasing temperatures and - at 175 °C - also with time. The greatest chloride ion generation was observed when water saturated o-dichlorobenzene reacted in the presence of iron oxides.In the presence of sulfuric acid the maximum chloride ion generation was detected at 175 °C and a sulfuric acid concentration of 3 · 10-3 mol/l.The hydrolysis products were monochlorobenzene and o-chlorophenol.The chloride ion generation from o-dichlorobenzene in neutral and slightly acid media is important when selecting materials of construction for chemical equipment.
    Notes: Die Hydrolyse von wassergesättigtem o-Dichlorbenzol und von o-Dichlorbenzol-Wasser-Gemischen wurde unter Lichtausschluß im neutralen und im sauren Bereich untersucht. Die Messungen wurden teils in Gegenwart von Rost bzw. metallischem Eisen durchgeführt.Die Chlorid-Abspaltung steigt mit zunehmender Temperatur und - bei 175 °C - auch mit zunehmender Beanspruchungsdauer an. Die höchste Chlorid-Abspaltung wurde bei wassergesättigtem o-Dichlorbenzol in Gegenwart von Rost gefunden.In Anwesenheit von Schwefelsäure tritt bei 175 °C ein Maximum der Chlorid-Abspaltung bei einer Schwefelsäure-Konzentration von 3 · 10-3 mol/l auf.Als Hydrolyseprodukte waren lediglich Monochlorbenzol und o-Chlorphenol nachweisbar.Die Chlorid-Abspaltung aus o-Dichlorbenzol im neutralen und schwach sauren Bereich ist bei der werkstofflichen Auslegung entsprechender Bauteile zu beachten.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Materialwissenschaft und Werkstofftechnik 13 (1982), S. 274-285 
    ISSN: 0933-5137
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Description / Table of Contents: The Formation of Surface Films and the Corrosion Resistance of the Silicon Containing Austenitic Steel X 2 CrNiSi 18 15 in Nitric AcidsThe oxide layers consist of two parts: the lower one is mainly Croxide, the upper one is SiO2. ESCA and AAS measurements were made in order to study the formation of the surface layer on the austenitic steel X2 CrNiSi 18 15 in nitric acids. A film, which is chromium oxide, is formed first. On top of this film a second film consisting of SiO2 grows. The elements nickel and manganese are not found in the formation of the oxide films. Immediately below the oxide layer the steel is enrichened with chromium and depleted of iron.In order to find the in some cases very small corrosion rates (5 · 10-5 mm · a-1) in a reproducible manner, the amounts of iron, chromium and nickel which had been dissolved were measured by means of the AAS method as a function of time.For stationary samples apparent activation energies of 65.2 kJ/Mol (azeotropic nitric acid) and 37.5 kJ/Mol (highly concentrated nitric acid), respectively, were found. These data confirm the assumption that the corrosion rate is determined by reactions at the phase boundaries.No appreciable influence of the flow velocity on the corrosion rate was detected.
    Notes: Mit Hilfe von ESCA- und AAS-Messungen wurde die Ausbildung der Deckschicht auf dem austenitischen Stahl X 2 CrNiSi 18 15 in Salpetersäuren untersucht. Es entsteht eine chromoxidreiche Deckschicht, über der sich eine SiO2-Schicht befindet. Nickel und Mangan sind am Aufbau der Oxidschichten nicht beteiligt. Unter der Oxidschicht wurde eine Chromanreicherung bzw. Eisenverarmung im Stahl nachgewiesen.Um die teilweise sehr geringen (bis 5 · 10-5 mm · a-1) Abtragungsraten reproduzierbar erfassen zu können, wurde in Lösung gegangenes Eisen, Chrom und Nickel in Abhängigkeit von der Beanspruchungsdauer mittels AAS bestimmt.Für ruhende Werkstoffproben ergaben sich scheinbare Aktivierungsenergien von 65,2 kJ/Mol (azeotrope Salpetersäure) bzw. 37,5 kJ/Mol (hochkonzentrierte Salpetersäure); diese Werte bestätigen die Annahme einer geschwindigkeitsbestimmenden Phasengrenzreaktion. Ein nennenswerter Einfluß der Fließgeschwindigkeit auf die Korrosion war nicht nachweisbar.
    Additional Material: 20 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 7 (1980), S. 457-463 
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Isotope dilution calibration curves for the quantitative analysis of organic compounds are determined at one point in time. Future analyses of unknowns are then referred to that single calibration. However, between the time that the calibration was performed and the time that the unknowns are analyzed, numerous changes in mass spectrometric operating conditions have often occurred. These include changes in resolution, mass discrimination, fragmentation patterns due to temperature changes, and electrometer offset. These changes will alter the mass spectrometric response and may reduce the accuracy and precision of the analysis. In order to investigate the effect of the above variations, a mathematical model has been developed which permits the influence of the operating conditions to be quantitated. The mass spectrometric response - i.e. isotope ratio - was very sensitive to changes in operating conditions. Changes in the isotope ratios of mixtures that were comprised predominantly of either the natural abundance compound or the labeled compound varied by up to 50%. However, the use of data reduction procedures that include a correction term for the isotope ratio of either or both of the natural abundance or labeled compound reduced the errors to 5% or less.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 9 (1982), S. 390-394 
    ISSN: 0306-042X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Geographic variations in the carbon isotope composition of the human diet and human hair were investigated. The carbon isotopic composition of common foodstufls purchased in Chicago, USA, Tokyo, Japan and Munich, FRG, were determined by combustion and differential isotope ratio mass spectrometry. The dietary protein carbon for the United States (-18.1‰) was calculated to be enriched in 13C relative to the Japanese (-21.2‰) and the German (-23.6‰) diets. To a large degree, the differences reflected the consumption of corn-fed animal products in the United States and Japan, as well as seafood in Japan. The carbon isotopic composition of hair (-16.4, -18.0 and -20.4%) for the three respective populations correlated with the calculated values of the dietary protein, but were 2-3% enriched in 13C. Changes in the isotopic composition of beard hair were shown to record the changes in dietary composition in travelers visiting the respective regions.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 11 (1984), S. 557-561 
    ISSN: 0306-042X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Natural differences in 13C/12C ratios of various metabolic fuels can produce systematic changes in the 13C/12C ratio of breath CO2, and therefore introduce errors into 13CO2 breath tests. To gain insight into the potential problem, we compared 13C/12C ratios of plasma macronutrients to those of breath CO2 under conditions that should alter the percentages of carbohydrate and lipid being oxidized. In rats, 48 h of starvation decreased the 13C/12C ratio of breath CO2 by 3.5‰. At this time the 13C/12C ratio of breath CO2 was very similar to that of plasma lipids. In humans, 30 min of heavy exercise increased the breath 13CO2/12CO2 ratio by 1.3‰. These changes in breath 13C/12C ratios could be predicted from 13C/12C ratios of plasma macronutrients and the percentage of carbon dioxide derived from each macronutrient, but only when compared within the same populations. For example, the 13C/12C ratios of plasma macronutrients of residents of Chicago, Illinois (USA) and Tokyo (Japan) differed by 1-3‰. An empirical correction of 13CO2 breath test data is recommended when breath tests are run under conditions that will change metabolic fuel utilization.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 9 (1982), S. 310-314 
    ISSN: 0306-042X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In order to determine the role of lactic acid as a metabolic substrate during exercise, the extent of its oxidation was studied using (13C)lactate under three different metabolic conditions in two subjects. During rest, easy exercise (work below the lactate inflection point), and hard exercise (work above the lactate inflection point), 100 mg of Na+-D,L(+)-2,3-(13C)lactate was injected via an indwelling catheter inserted in an antecubital vein. Blood as well as expired gas samples were collected up to 2 h post-injection. Subjects worked at average intensities of 53% and 74% VO2max during easy and hard exercise, respectively. During rest and easy exercise, blood lactate concentrations remained stable at 1-2 mM. During hard exercise, blood lactate increased to 3-4 times those observed at rest. Excretion of 13CO2 peaked much sooner and enrichment of 13C in CO2 was greater during both exercise intensities than during rest. Cumulative recovery of injected 13C as 13CO2 averaged 13.2 and 86.2% through 120 min during rest and easy exercise. Through 45 min of hard exercise, recovery of tracer as CO2 was the same as during a similar time point of easy exercise, 51.8%. The results support the contention that oxidation is the major fate of lactate during exercise.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: No Abstract.Das vollständige Manuskript dieser Zuschrift erscheint in: Angew. Chem. Suppl. 1982, 1992-2003
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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