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  • 1
    ISSN: 1520-510X
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1520-510X
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Industrial & engineering chemistry research 31 (1992), S. 29-37 
    ISSN: 1520-5045
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Polymer bulletin 6 (1982), S. 471-476 
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary The production of oligomers — to a degree of polymerization 5 — during acid hydrolization of polymer dextrans was estimated quantitatively by a combined aqueous SEC and adsorption separation. It was found that the molar concentrations of the oligomers were higher for those with lower DP. This experimental result is in agreement with a degradation model, in which the molecular weight decreases with the power of 2/3 versus time, which has been proposed earlier.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1572-901X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary 2-Acetylpyridine N(4)-dihexyl- and N(4)-dicyclohexylthiosemicarbazone, HAc4DHex and HAc4DCHex, respectively, and FeIII, CoII, CoIII, NiII, CuII and ZnII complexes have been prepared and characterized by molar conductivities, magnetic susceptibilities and spectroscopic techniques. For many of the complexes, loss of the N(2)H hydrogen occurs, and the ligands coordinate to the metal centres as NNS monoanionic, tridentate ligands, e.g., [M(NNS)X] (M = CoII, NiII, CuII, NNS = Ac4DHex or Ac4DCHex and X = Cl or Br), [Fe(NNS)2]ClO4, [Co(NNS)2]BF4, [Cu(NNS)NO3] and [Zn(NNS)OAc]. ZnII ion is also chelated by neutral ligands in [Zn(HNNS)X2] (X = Cl, Br). In addition, [Ni(Ac4DHex)-(HAc4DHex)]X (X = BF4, ClO4) and [Ni(HAc4DCHex)2]-(BF4)2 are reported where the neutral thiosemicarbazone is coordinated via the pyridyl nitrogen, azomethine nitrogen and thione sulfur. Crystal structure determinations of HAc4DCHex and [Cu(Ac4DHex)Br] show the former to contain the bifurcated hydrogen bonded form and the latter to be planar with no significant interaction between neighbouring centres.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Chemical Engineering & Technology - CET 13 (1990), S. 241-251 
    ISSN: 0930-7516
    Keywords: Chemistry ; Industrial Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Pyrolysis of 2,3-dimethyl butane (DMB) was carried out in a quartz flow reactor in the temperature range from 740 to 1032 K at normal pressure. The input concentration of DMB was 3.3 × 10-3 mol/1 using argon as diluent. Reaction time ranged between 3.1 and 3.9 s. The following products were analyzed by two-column gas chromatography: hydrogen, methane, ethene, propane, propene, butenes, butadiene, 2-methyl-2-butene, isoprene, benzene and toluene. Compared to thermal decomposition of n-hexane under similar experimental conditions, the main difference concerned the formation of ethylene, ethane and branched alkanes. A reaction model, based on elementary reactions, was developed to predict the experimental results and to verify our data basis of elementary reactions under different conditions. The model gives a quantitative description of the complex chemistry of the process. In addition, an algorithm is presented for model reduction.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 176 (1975), S. 745-757 
    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: The degradation reaction of dextran by the action of ultrasound was investigated within the molecular weight range from 30 000 to 90 000 in different solvents. The degradation products were characterized by their molecular weight distributions obtained by chromatography on porous glass. From the results of the experiments it could be shown that degradation follows a first order reaction, that the rate constant of degradation is proportional to the molecular weight, and that the molecules break preferentially into two parts of approximately equal size. The nature of the solvent has a considerable effect on the rate constants, which could be shown to be proportional to the enthalpy of vaporization of the solvent. The effect of polymer conformation on the degradation constants was studied and it was found that the degradation constants increase with expansion of the polymer coils.The experimental results confirm the general assumption, that the cavities, which are caused by ultrasound, are responsible for the degradation reaction. It is not possible, however, to conclude from the experimental results known so far, whether the inhomogenous flow fields or the shock waves, which arise from the collapse of cavitation bubbles, are responsible for the rupture of the molecule. The experimental result, that expanded polymer coils are more easily degraded. favours the mechanism which implies shock waves. Furthermore, a model in which both effects are acting together, in the way that the inhomogeneous flow fields at first stretch the polymer coil, whereas the shock wave, which immediately follows, breaks the molecule, is suggested to explain the rupture of the molecules.
    Notes: Die Abbaureaktion von Dextran durch Ultraschall wurde im Molekulargewichtsbereich von 30 000 bis 90 000 in verschiedenen Lösungsmitteln untersucht. Die Abbauprodukte wurden durch ihre Molekulargewichtsverteilungen, die mit Hilfe von Chromatographie an porösem Glas bestimmt wurden, charakterisiert. Aus den Ergebnissen der Untersuchungen konnte abgeleitet werden, daß die Abbaureaktion nach erster Ordnung verläuft, die Abbaukonstante proportional dem Molekulargewicht ist, und die Moleküle bevorzugt in zwei nahezu gleichgroße Bruchstücke zerfallen. Die Art des Lösungsmittels hat dabei einen erheblichen Einfluß auf die Abbaukonstanten; es wurde gefunden, daß diese der molaren Verdampfungsenthalpie des Lösungsmittels direkt proportional sind. Der Einfluß der Konformation des Polymeren auf die Abbaukonstanten wurde studiert, wobei sich ergab, daß mit einer Aufweitung der Polymerknäuel die Abbaukonstanten größer wurden.Die Ergebnisse bestätigen die allgemeine Auffassung, daß die Kavitäten, die bei der Ultrabeschallung entstehen, für die Abbaureaktion verantwortlich sind. Eine eindeutige Entscheidung, ob die inhomogenen Strömungsfelder oder die Stoßwellen, die bei der Implosion der Kavitäten entstehen, für den Molekülbruch letztlich maßgebend sind, kann mit den bisher vorliegenden Ergebnissen nicht getroffen werden. Der Befund, daß aufgeweitete Knäuel leichter abgebaut werden, spricht für den Stoßwellenmechanismus. Andererseits wird ein Modell für die Abbaureaktion angegeben, in dem beide Effekte insoweit zusammenwirken, daß die inhomogenen Strömungsfelder das Polymerknäuel zunächst strecken und die nachfolgende Stoßwelle den Molekülbruch bewirkt.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 183 (1982), S. 1207-1218 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The thermal degradation of polydisperse polystyrene samples with mol. wts. (M̄n) between 60000 and 22000 has been investigated at different temperatures under oxygen free conditions. Product analysis has been carried out by GPC. The experimental degradation could be simulated by a model consisting of scission and depolymerization. The dynamical behaviour of this model is expressed in a matrix from. The ratio of scission and depolymerization is constant for all polymers and different temperatures during degradation. Therefore, a master curve could be evaluated, which gives a general relation between the decrease of mol. wt. and the mass of volatiles. Finally a radical chain mechanism has been proposed in a lumped form which is consistent with the kinetic model and the experimental results.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 188 (1987), S. 561-582 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The thermal behavior of polydisperse poly(p-methylstyrene) (PPMS) samples with M̄w's of 99200 and 356000 g/mol was investigated under oxygen-free conditions at temperatures between 220 and 345°C. The reaction products were analysed by gel permeation chromatography (GPC), gas chromatography (GC) and swelling measurements. In the initial stage of the reaction crosslinking occurs; at higher temperatures the gel decomposes to polymers with a low degree of polymerization and to volatile products with molecular weights in the range up to trimers. A radical chain mechanism is proposed for degradation which explains the experimental results. On this basis a model is evaluated for gel formation, which is discussed in detail. The results of the present investigation are compared with the thermal degradation of polystyrene (PS) which is chemically similar but does not crosslink.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 185 (1984), S. 991-1001 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Thermal degradation of polystyrene (PS) was carried out in the absence of oxygen between 292 and 336°C. The formed volatile products were analysed qualitatively and quantitatively by means of gas charomatography. It was found that the composition of the volatile fraction is a function of conversion and independent of temperature for most of the products. A radical chain mechanism is proposed to explain these experimental results.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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