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  • 1
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Phytochemistry 27 (1988), S. 653-655 
    ISSN: 0031-9422
    Keywords: 3',4'-dihydrostephasubine ; Menispermaceae ; Stephania hernandifolia ; bisbenzylisoquinoline alkaloid ; epistephanine. ; stephasubine
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Phytochemistry 26 (1987), S. 2391-2395 
    ISSN: 0031-9422
    Keywords: Menispermaceae ; Stephania suberosa ; delavaine ; nordelavaine ; promorphinane hasubanane alkaloid ; stephanubine. ; stephaphylline
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0031-9422
    Keywords: Menispermaceae ; Stephania venosa ; aporphine alkaloid ; kamaline.
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 4
    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 reactivity ratios, thermal behavior, and the bacteriocidal properties of the resins prepared from substituted acetophenones, i.e., m-aminoacetophenone, o-hydroxyacetophenone, and m-hydroxyacetophenone, have been investigated. The results obtained from the bacteriocidal studies are found to be quite interesting. Some of the resins synthesized are potent bacteriocides. The simple Kelen - Tüdös linear graphical method was used to determine the order of reactivity of substituted acetophenones when they are copolymerized with halogen-substituted anilines, i.e., o-chloroaniline, m-chloroaniline, and p-chloroaniline. The resins are found to be thermally stable and the energy of activation have been evaluated from TG curve by applying the Freeman - Anderson and Broido methods.
    Additional Material: 6 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Chemistry and Physics 199 (1998), S. 311-317 
    ISSN: 1022-1352
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The effect of an organized anionic surfactant, i.e. sodium dodecyl sulfate (SDS), on the acrylamide (AM) polymerization initiated with the redox system Ce(IV)-cyclohexanone (CH) in aqueous nitric acid was kinetically studied over a temperature range of 25-45°C. With increasing concentration of SDS, above its critical micelle concentration (CMC) the rate of polymerization, Rp(obs), as well as the rate of Ce(IV) consumption, -RCe(obs), were found to increase, while in the presence of cetyltrimethylammonium bromide (CTAB) these rates decreased considerably. Rp(obs) is proportional to [Ce(IV)]0.5, [CH]0.5 and [AM]1.5. -RCe(obs) also increases with increasing concentration of Ce(IV), cyclohexanone and acrylamide. The overall activation energy for the process, in the presence and absence of 15 × 10-3 M of SDS, was calculated to be 15.1 and 21.4 kcal/mol, respectively. The viscosity average molecular weight of polyacrylamide was found to increase with increasing SDS concentration. A suitable mechanistic scheme for the polymerization process is proposed.
    Additional Material: 6 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 52 (1994), S. 1557-1568 
    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 influence of N-acetylglycine on the kinetics of graft copolymerization of acrylonitrile (AN) and methyl methacrylate (MMA) onto chemically modified jute fibers was studied in the temperature range 40-60°C. The optimum conditions for grafting have been determined by studying the effects of concentrations of monomers, Ce(IV), and N-acetylglycine on the rate of grafting. Besides the effect of time, temperature, and concentration of the acid, the amount of jute fibers and some organic solvents and inorganic salts on the rate of grafting has been investigated. On the basis of experimental findings, a kinetic scheme has been proposed. Infrared spectra of chemically modified jute and grafted jute have been investigated. More than 185% graft yield could be achieved with the present system. Grafting has improved the thermal stability of jute fibers. © 1994 John Wiley & Sons, Inc.
    Additional Material: 7 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 62 (1996), S. 19-25 
    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 polymerization of acrylonitrile (AN) using the Ce(IV)-citric acid (CA) redox system as an initiator in aqueous nitric acid solution, in the presence of an anionic surfactant, sodium dodecyl sulfate (SDS), has been kinetically studied at a temperature range of 25-45°C. The rate of polymerization (Rp) and disappearance of Ce(IV) (-Rce) increase with increasing concentration of SDS, above its critical micelle concentration (cmc), when the surfactant molecules are organized. Rp was found to be proportional to [AN]1.5 and [CA]0.5. With other organic substrates, Rp follows the increasing order of sorbitol ≥ mannitol 〉 glycerol 〉 CA. But it was found to decrease considerably in the presence of cationic surfactant (CTAB), and nonionic surfactant (Triton-X-100) had no effect on the rate. -Rce varies linearly with [Ce(IV)] and [CA]. Both Rp and -Rce increase with increasing temperature. The overall activation energy was found to be 18.31 and 13.72 kcal/mol in the absence and presence of 0.015M SDS, respectively. The chain length of the polyacrylonitrile has also increased with increasing SDS concentration. © 1996 John Wiley & Sons, Inc.
    Additional Material: 5 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 52 (1994), S. 1549-1556 
    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 micellar effect on the kinetics of ceric ion-initiated polymerization of acrylonitrile (AN) in the presence of N-acetylglycine has been studied in the temperature range 30-50°C. The neutral emulsifier (Triton X-100) has no effect on the Rp, whereas both anionic (NaLS) and cationic (NCTAB) emulsifiers accelerate the rate of polymerization appreciably. Comparison of the effect of different organic substrates on the rate of polymerization has been made. Various effects such as the concentration of metal ion, surfactant, monomer, sulfuric acid, organic solvents, and inorganic salts on Rp have also been investigated. The most remarkable feature of the investigation involves the enhancement of Rp in the presence of micelles. A suitable mechanism for the derivation of the rate expression for the above system is proposed along with the calculation of activation energy and prediction of optimum conditions. © 1994 John Wiley & Sons, Inc.
    Additional Material: 6 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 32 (1986), S. 5071-5083 
    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: A number of resins were prepared by condensing m-aminoacetophenone with substituted aromatic compounds and formaldehyde in the presence of acids and bases as catalyst. The resins were characterized by infrared spectra. The solubility parameters were calculated from Small's group contribution which agreed well with the experimental value. The bacteriocidal properties of the resins have been studied.
    Additional Material: 4 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 144 (1986), S. 23-37 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Neue Harze wurden aus o-Hydroxyacetophenon durch Reaktion mit substituierten aromatischen Verbindungen und Formaldehyd in Anwesenheit verschiedener Säuren und Basen als Katalysatoren nach zwei Verfahren hergestellt. Die Polymeren wurden mit Hilfe der IR-Spektroskopie charakterisiert. Die thermischen, chemischen und Lösungseigenschaften der Harze, die nach der Methode von Small berechnet wurden, stimmen gut mit den experimentell ermittelten Werten überein. Die Harze sind ziemlich thermostabil, und die Aktivierungsenergie wurde aus der Thermogravimetriekurve nach Freeman-Anderson und Broido bestimmt.
    Notes: New resins have been synthesized from o-hydroxyacetophenone by reaction with substituted aromatic compounds and formaldehyde in the presence of various acids and bases as catalyst following two different techniques. The polymer samples are characterized by IR spectra. The solution, thermal, and chemical properties of the resins are investigated. The solubility parameters of the resins calculated according to the investigations of Small agree well with the experimental values. The resins are found to be fairly thermostable and the energy of activation is evaluated from TG curve by applying (i) Freeman-Anderson method and (ii) Broido method.
    Additional Material: 6 Ill.
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