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  • Chemistry  (15)
  • Computer Systems  (10)
  • 1995-1999  (19)
  • 1965-1969  (4)
  • 1925-1929  (2)
  • 1
    Electronic Resource
    Electronic Resource
    Ultrasonic degradation of macromolecules in solution. Study of degradation kinetics by estimation of free-radical scavenger DPPH and solution viscosity measurementsProd. No. 1357 (1966)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 10 (1966), S. 1089-1098 
    Details
    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 kinetics of degradation of butyl rubber in two solvents, cyclohexane and toluene, was studied by two independent techniques: viscosity measurements and free-radical estimation as a function of DPPH consumed. The general shape of the rate curves in the two cases is similar, but not identical. The rate given by estimation of DPPH is faster than that obtained from solution viscosity data. This has been attributed to the inherent limitations of the two methods for the quantitative determination of the number of breaks occurring in the polymer molecules. The rate is also reduced as the viscosity of the solution medium is increased, which may be correlated with the reduction of the cavitation effect responsible for degradation. The degradation rates in two solvent media initially having the same viscosity were unequal. This may be due to different solvent-solute characteristics, which means that the viscosity and cavitation change to different extents in the two cases throughout the course of degradation. The limiting degree of Polymerization (DP)∞ obtained after prolonged irradiation has been found to be dependent on parameters such as intensity of irradiation, solution viscosity, and initial DP of the molecules.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1966.070100801
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  • 2
    Electronic Resource
    Electronic Resource
    Gas treatment in trickle-bed biofilters: Biomass, how much is enough? (1997)
    New York, NY [u.a.] : Wiley-Blackwell
    Biotechnology and Bioengineering 54 (1997), S. 583-594 
    Details
    ISSN: 0006-3592
    Keywords: trickle-bed biofilter ; mathematical model ; volatile organic compound (VOC) ; waste gas treatment ; biofiltration ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: The objective of this article is to define and validate a mathematical model that desribes the physical and biological processes occurring in a trickle-bed air biofilter for waste gas treatment. This model considers a two-phase system, quasi-steady-state processes, uniform bacterial population, and one limiting substrate. The variation of the specific surface area with bacterial growth is included in the model, and its effect on the biofilter performance is analyzed. This analysis leads to the conclusion that excessive accumulation of biomass in the reactor has a negative effect on contaminant removal efficiency. To solve this problem, excess biomass is removed via full media fluidization and backwashing of the biofilter. The backwashing technique is also incorporated in the model as a process variable. Experimental data from the biodegradation of toluene in a pilot system with four packed-bed reactors are used to validate the model. Once the model is calibrated with the estimation of the unknown parameters of the system, it is used to simulate the biofilter performance for different operating conditions. Model predictions are found to be in agreement with experimental data. © 1997 John Wiley & Sons, Inc. Biotechnol Bioeng 54: 583-594, 1997.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    A modeling study of anaerobic biofilm systems: I. Detailed biofilm modeling (1995)
    New York, NY [u.a.] : Wiley-Blackwell
    Biotechnology and Bioengineering 46 (1995), S. 43-53 
    Details
    ISSN: 0006-3592
    Keywords: acetate ; anaerobic biofilms ; mass transfer ; pH ; biofilm modeling ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: A detailed model acetate-utilizing methanogenic biofilms accounting for the diffusion of neutral and ionic species, chemical equilibrium, electroneutrality, gas production within the biofilm, pH-dependent Monod kinetics, and the presence of a concentration boundary layer is presented. The model qualitatively fits the pH profiles that are reported for acetate-utilizing methanogenic aggregates. A sensitivity analysis on the biological parameters showed that the flux of acetate is sensitive to the maximum utilization rate, half-saturation constant, and biofilm density for the bulk conditions investigated. Criteria when traditional biofilm models can be used to predict the flux of acetate into the biofilm are established. If the maximum pH change predicted using a hypothetical system is within ±0.05, the traditional model predicts the flux to within ±5% of the value calculated with the model developed in this study. © 1995 John Wiley & Sons, Inc.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/bit.260460107
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  • 4
    Electronic Resource
    Electronic Resource
    A modeling study of anaerobic biofilm systems: II. Reactor modeling (1995)
    New York, NY [u.a.] : Wiley-Blackwell
    Biotechnology and Bioengineering 46 (1995), S. 54-61 
    Details
    ISSN: 0006-3592
    Keywords: anaerobic biofilm ; CSTR ; reactors, nonide ; pH ; plug-flow reactors ; biofilm modeling ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: A rigorous steady-state model of anaerobic biofilm reactors taking into account acid-base and gas-phase equilibria in the reactor in conjunction with detailed chemical equilibria and mass transfer in acetate-utilizing methanogenic biofilms is presented. The performances of ideal completely stirred tank reactors (CSTRs) and plug-flow reactors, as well as reactors with nonideal hydraulic conditions, are simulated. Decreasing the surface loading rate increases the acetate removal efficiency, while decreasing the influent pH and increasing the buffering capacity improves the removal efficiency only if the bulk pH of the reactor shifts toward more optimal values between 6.8 to 7.0. The reactor can have negative or positive removal efficiencies depending on the start-up conditions. The respiration coefficient plays a critical role in determining the minimum influent pH required for reactor recovery after failure. Having multiple CSTRs-in-series generally increases the overall removal efficiency for the influent conditions investigated. Monitoring of the influent feed quality is critical for plug-flow reactors, becasue failure of the initial sections of the reactor may cause a cascading effect that may lead to a rapid reactor failure. © 1995 John Wiley & Sons, Inc.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/bit.260460108
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  • 5
    Electronic Resource
    Electronic Resource
    Chemiluminescenz bei der Oxydation von Farbstoffen durch Ozon (1928)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 173 (1928), S. 125-136 
    Details
    ISSN: 0863-1786
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 1. Wenn ozonisierter Sauerstoff durch Lösungen von Eosin, Uranin, Safranin, Neutralrot, Rhodamin B, Thioflavin, Cartharamin Rhodamin B. J. N. N., Erythrosin und Aesculin geleitet wird, beobachtet man ein Leuchten.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19281730114
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  • 6
    Electronic Resource
    Electronic Resource
    Chemiluminescenz bei der Oxydation von fluorescierenden und nicht fluorescierenden Stoffen durch Wasserstoffperoxyd und Ozon (1929)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 186 (1929), S. 154-158 
    Details
    ISSN: 0863-1786
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 1. Wenn zahlreiche fluorescierende oder nicht fluorescierende Farbstofflösungen durch Wasserstoffperoxyd in Gegenwart von Ferrosulfat oxydiert werden, tritt ein Glimmen auf, das im dunklen Raume zu erkennen ist.2. Die Wellenlangen der Glimmerscheinung bei der Oxydation einiger fluorescierender Fnrbstoffe durch ozonisierten Sauerstoff sind gemessen worden.3. Kieselsaure mit etwas adsorbiertem Neutralrot zeigt in einer Suspension in Äthylallrohol bei Behandlung mit ozonisiertem Sauerstoff eine Glimmerscheinung.4. Wenn kleine Mengen eines Farbstoffes, der gutes Glimmen zeigt , rnit einem anderen Farbstoff von schwachem Glimmvermogen gemischt werden, so liefert das Gemisch bei Behandlung mit Ozon ein starkeres Glimmen als der schwächer glimmende Farbstoff allein.5. Steigerung der Temperatur führt zur Verstarkung des Glimmens bei der Oxydation von Reduktionsmitteln durch Ozon oder Wasserstoffperoxyd.6. Zunahme der Konzentration der Reduktionsmittel verursacht eine Steigerung der Glimmintensitat bis zu einem Grenewert. Wird die Konzentration weiter gesteigert, so schwacht sich das Glimmen ab und hört schließlich auf.
    Additional Material: 4 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19291860111
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  • 7
    Electronic Resource
    Electronic Resource
    Polymerization of N-vinylearbazole with vanadium compounds. Part I. Polymerization with vanadium pentoxide and metal vanadates (1969)
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 124 (1969), S. 263-273 
    Details
    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: In Gegenwart von Vanadiumpentoxid als heterogenern Katalysator Wurde N-Vinylcarbazol (NVC) in Substanz polymerisiert. Die Polymerisationsgeschwindigkeit hängt vom Verhältnis des Katalysators zum Monomeren ab. Es wurde ein kationischer Reaktionsmechanismus vorgeschlagen, und es wurde versucht, die Rolle der V2O5-Oberfläche bei der Polymerisation aufzuklären. Es wird vermutet, daß die π-Säureeigenschaft des V5⊕-Ions bei der Initiierung der Polymerisation miteinbezogen werden muß.Die Wirkung einer Anzahl von Zusätzen auf die Polymerisationsgeschwindigkeit wurde untersucht; das Ergebnis bekräftigt die Annahme eines kationischen Verlaufs.Es wurde auch die katalytische Wirksamkeit einer Anzahl von Metallvanadaten bei der Polymerisation von NVC untersucht. Es ergab sich eine hinreichend gute Bezichung zwischen der katalytischen Wirksamkeit und dem elektronegativen Charakter des metallischen Bestandteils.
    Notes: Bulk polymerization of N-Vinylcarbazole (NVC) has been carried out using vanadium pentoxide as the contact catalyst. The rate of polymerizatlon has been found to depend upon catalyst to monomer ratio. A cationic mechanism has been suggested and the role of V2O5 surface in the polymerization has been tentatively analyzed. The π-acid characteristies of V5⊕ ion is believed to be involved in initiating the polymerization. The effect of a number of additives on the polymerization rate has been studied, which endorses the cationic mechanism. The catalytic efficiency of a number of metal vanadates for the polymerization of NVC has also been studied. A fairly good correlation between the activity and electronegativity of the metallic moiety has been established.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/macp.1969.021240127
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  • 8
    Electronic Resource
    Electronic Resource
    Interaction of polylysine with phosvitin and nucleic acids (1969)
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 124 (1969), S. 113-117 
    Details
    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 DNS-abhängige RNS-Synthese wird durch basische Proteine, wie Histone oder Polylysin, gehmmt: es wurde gefunden, daß dieser Hemmungseffekt durch Phosvitin, ein phosphoprotein, aufgehoben wird. Turbidimetrische Untersuchungen ergaben, daß Polylysin mit DNS iind RNS in stöchiometrischem Verhältnis reagiert.Es wird angenommen, daß diese Reaktion mit DNS die Ursache des Hemmungseffektes ist. Noch wirksamer als DNS reagiert Phosvitin mit Polylysin. Phosvitin kann in viel geringerer als der stöchiometrischen Menge mit DNS um Polylysin konkurrieren, also DNS freisetzen und als Matrize für die RNS-Synthese verfügbar machen. Phosphoserin ist, im Gegensatz zu Phosvitin, unwirksam bei der Aufhebung des Hemmungseffektes von Polylysin.
    Notes: DNA dependent RNA asynthesis in inhibited by basic proteins like histones or polylysine This inhibitory effect is found to be suppressed by phosvitin, which is a phosphoprotein. Turbidometric studies indicate that polylysine interacts with DNA and RNA stoichiometrically. This interaction with DNA has been thought to be the cause of this inhibitory effect. Phovitin also interacts with polylysine more effectively than DNA. Phosvitin in quantities much less than the stoichionietric amount can compete with DNA for the polylysine and can thus make DNA free and available as template for the RNA synthesis. Phosphoserine, unlike pbosvitin, is ineffective in suppressing the inhibitory effect of polylysine.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/macp.1969.021240112
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  • 9
    Electronic Resource
    Electronic Resource
    Polymer-anchored metal complexes. III. Preparation, structural, thermal stability, dielectric, and conductivity characterization of polycondensates from Cu(II)-1, 10-phenanthroline and trimellitic anhydride/pryromellitic dianhydride (1995)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 56 (1995), S. 501-508 
    Details
    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: Trimellitic anhydride and pyromellitic dianhydride have been polycondensed with Cu(II)-phenanthroline complex as a comonomer in the presence of anhydrous ZnCl2 under selective conditions. Elemental diffuse reflectance and infrared spectroscopic and X-ray diffraction (XRD) analysis data of these polymers have been correlated with the tentative structure Proposed for these polycondensates. Thermal stability and dielectric and conductivity characteristics of these polycondensates have been evaluated to understand the effect of the ligand and the anhydride moieties on these properties. Unlike the polymer-anchored 3d-metal complexes, these polycondensates fail to initiate the cationic polymerization of N-vinylcarbazole. © 1995 John Wiley & Sons, Inc.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1995.070560412
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  • 10
    Electronic Resource
    Electronic Resource
    Ferric chloride-initiated polymerization of pyrrole in presence of N-vinyl carbazole in aqueous suspension (1996)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 60 (1996), S. 143-146 
    Details
    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
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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