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  • Chemistry  (3)
  • modification  (3)
  • flavour  (2)
  • 1
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Phytochemistry 29 (1990), S. 745-747 
    ISSN: 0031-9422
    Keywords: Chlorophyceae ; Ulva pertusa ; fatty acids ; flavour ; long-chain aldehydes ; marine green alga ; protoplasts ; regeneration ; sterility test.
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0031-9422
    Keywords: Ulva pertusa ; Ulvaceae ; aldehydes ; fatty acids. ; flavour ; marine green alga
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 272 (1994), S. 1620-1626 
    ISSN: 1435-1536
    Keywords: Zeolite ; modification ; chloroform ; adsorption
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Adsorption characteristics of chloroform from its aqueous solution on Na−Y and Li−Na−Y modified by SiCl4 were measured and compared with those on Na−ZSM-5 and Na-Mordenite. No adsorption occurred on Na−Y with high hydrophilicity, while the siliceous faujasites became capable of adsorption and its amount increased with increase in the Si/A1 ratio. Adsorption isotherms are of Langmuir type, suggesting that adsorption proceeds by pore filling. The adsorption amounts expressed in volume on Na−Y with high hydrophobicity corresponded to their pore volumes. Adsorption characteristics of chloroform from gaseous phase on Na−Y with different Si/A1 ratio were also measured. The adsorption capability decreased with increasing Si/A1 ratio. Immersional heats of zeolites into water or chloroform were measured in order to evaluate the surface affinity to both solvents. Immersional heats into water were almost constant (about 500 mJ·m−2) for zeolites with their Si/A1 ratio below 10. The heats decreased with an increase in the Si/A1 ratio above 10, then became almost constant (about 120 mJ·m−2) over 30 in their ratio. Heats of immersion of Na−Y series into chloroform were almost constant irrespective of their Si/A1 ratio, but decreased slightly when the ratio exceeded 20. Adsorption characteristics of chloroform could be well related to immersional heats into both solvents.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 272 (1994), S. 830-836 
    ISSN: 1435-1536
    Keywords: Zeolite ; modification ; surfactant ; adsorption
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Hydrophobic faujasite-type zeolites were prepared by the treatment of hydrophilic Na-Y4.6 with silicon tetrachloride (SiCl4) by way of dealumination-silicon exchange reaction. Hydrophilic-hydrophobic characters of these zeolite surfaces were evaluated by measurements of immersional heats into water orn-hexane. Adsorption rates of sodium dodecylsulfate (SDoS) on these zeolites from its aqueous solution and their adsorption characteristics were investigated, and compared with those on ZSM-5 with various Si/Al ratios. The adsorption ability of SDoS into zeolite micropores developed on the zeolite only when it was modified to some extent. The adsorption rates of SDoS were very slow and proved to be affected by molecular diffusion in zeolite pores. They depended on hydrophilic-hydrophobic character of zeolites as well as on pore structures. Adsorption isotherms of SDoS were of Langmuir type, which indicates that the adsorption occurred typically into zeolite pores. Adsorbed amount of SDoS depended on the balance of hydrophilic-hydrophobic character and number of cation site of zeolite surfaces, and had a maximum in case of ZSM-5 zeolites.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 273 (1995), S. 787-792 
    ISSN: 1435-1536
    Keywords: Zeolite ; modification ; surfactant ; adsorption
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Adsorption characteristics of anion-, cation- and nonion-type surfactants and phenol from their aqueous solution on Na-Y zeolites modified by SiCl4 treatment and NA-ZSM-5 zeolites with several Si/Al ratios were measured. Surfactants used were sodium dodecylbenzenesulfonte (DBS), laurylpyridinium chloride (LPC), polyoxyethylenenonylphenylether (POENPE) and phenol. Adsorption of surfactants was enhanced by SiCl4 treatment of Na-Y, which indicates an important role of the hydrophilic-hydrophobic character in the adsorption. Adsorption isotherms were in general of Langmuir type and adsorbed amount depended on the Al/(Si+Al) or Si/Al ratio of zeolite frameworks. In case of DBS adsorption of Na-ZSM-5 series, adsorption occurred only on the outer surface due to steric hindrance. LPC adsorption abilities were observed on even hydrophilic zeolites and were ascribed to ion exchange effect. In case of phenol adsorption on hydrophobic Na-Y, the adsorption isotherm was of Type V according to BDDT classification.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 180 (1979), S. 825-828 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 128 (1969), S. 63-82 
    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: Um die Möglichkeit zur Bildung von Polymerkristallen mit gestreckten Ketten, die sich im Verlauf der Polymerisation bilden, zu ergründen, wurde die kationische Polymerisation von Trioxan in Cyclohexan untersucht. Das Polymere - Polyoxymethylen - wurde in Form neuartiger Einkristalle erhalten. Sowohl aus den morphologischen und physikalischen Untersuchungen der erhaltenen Polymeren als auch aus kinetischen Untersuchungen der Polymerisation ging hervor, daß die langen, nadelartigen Keime, die sich zu Beginn der Polymerisation bilden, unter Zwillingsbildung zu federartigen Plättchen wachsen. Aus den Dichtemessungen ergab sich der Kristallinitätsgrad der entstehenden Polymeren zu 100% Die Molekülketten waren völlig gestreckt und regelmäßig in der Richtung des Kristallwachstums angeordnet. Das Wachstum des Kristalls verläuft in dem Maße, wie die Polymerisation fortschreitet. Es wird daher angenommen, daß der Kristall direkt durch das Kettenwachstum weiterwächst, das seinerseits durch die Addition der monomeren Moleküle an die aktiven Kettenenden eintritt, die zweidimensional auf der wachsenden Oberfläche des Kristalls angeordnet sind. Jedoch stimmt die Kettenlänge des gebildeten Polymeren, die aus der Viskosität der Lösung ermittelt wurde, nicht überein mit den Dimensionen des Kristalls, gemessen in der kristallographischen Kettenrichtung, d. h., die viskosimetrisch ermittelte Kettenlänge war viel kleiner. Die obengenannten Ergebnisse werden durch Kettenübertragungsreaktionen und durch die katalytische Zersetzung der polymeren Kette erklärt.
    Notes: In order to pursue the possibility of the extended chain crystals of polymers formed in the course of polymerization, the cationic polymerization of trioxane in cyclohexane has been studied. The polymer, polyoxymethylene, was obtained in the form of a unique single crystal. From the morphological and physical studies of the resultant polymers as well as the kinetical studies of the polymerization, it has been revealed that long, needle-like nuclei formed in the beginning of the polymerization grew into feather-like platelets with twin habit. The degree of crystallinity of the nascent polymer was essentially 100% in terms of their densities. The molecular chains were fully extended and regularly aligned in the direction of the crystal growth. The growth of the crystal occurred as the polymerization proceeded. Thus it is considered that the crystal grows quite successively to the propagation of the chains through direct addition of the monomer molecules onto the reactive chain ends which are aligned two-dimensionally on the growing surface of the crystal. The molecular length of the nascent polymer estimated from the solution viscosity, however, did not agree with the crystal dimensions measured in the direction of the molecular orientation, the former being rather small. The above results are explained in terms of the chain-transfer reaction and the catalytic decomposition of the polymer chain.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Letters 2 (1964), S. 333-337 
    ISSN: 0449-2986
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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