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  • 2000-2004  (1)
  • 1985-1989  (2)
  • electrochemical and fluorescent probes  (2)
  • Aphelenchus avenae  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 264 (1986), S. 896-902 
    ISSN: 1435-1536
    Keywords: Microemulsions ; viscosity ; electrical conductivity ; electrochemical and fluorescent probes
    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 Microemulsion systems involving brine and dodecane, and stabilized by sodium dodecylsulfate and both pentanol and heptanol have been investigated. Results of various experiments including conductivity and viscosity measurements, electrochemical diffusion coefficients and fluorescent probe studies have been gathered and compared in order to gain additional understanding of the microemulsion structure. The diffusion coefficients of hydrophilic hydroquinone and hydrophobic ferrocene obtained from the Levich equation at the rotating disc electrode, vary as the self-diffusion coefficients of water and dodecane, respectively; the results are consistent with those obtained by other workers from tracer or NMR self-diffusion studies. The fluorescence analysis of the polarity sensed by pyrene and the microviscosity felt by dipyrenylpropane suggests that the progressive addition of pentanol and dodecane to SDS micelles leads to solubilizate the probes more in the droplet interior where they experience a more hydrophobic environment. The systematic study of the two microemulsion systems provides insight into the microscopic properties of the oil domains in which the fluorescent probes are assumed to be located. In the system stabilized by n-heptanol as cosurfactant, the microviscosity sensed by P(CH2)3P is shown to be much lower than the bulk viscosity of the microemulsion. All the results evidence the well-known structural transitions: water continuous, bicontinuous and oil continuous in the single monophasic area of the brine/ SDS/n-pentanol/dodecane system; premicellar aggregates and water swollen micelles in the W/O area of the brine/SDS/n-heptanol/dodecane system.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1435-1536
    Keywords: Microemulsions ; viscosity ; conductivity ; electrochemical and fluorescent probes
    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 The properties of pseudo-ternary systems involving brine, sodium dodecylsulfate (SDS), pentanol and dodecane or hexane have been investigated. When the hydrocarbon is dodecane, the microemulsion system includes in addition to the main monophasic area a small lens inserted in an oil-rich zone. With hexane, the microemulsion domain splits into two parts, one of which consists of a narrow scythe-blade shaped area which spreads from the water top up to compositions very rich in hydrocarbon. The properties of these uncommon microemulsions were compared with those of microemulsions belonging to the main monophasic area in order to gain additional understanding of their structure. Results of experiments including electrical conductivity and viscosity measurements, electrochemical and fluorescent probe studies lead to the following conclusions: Microemulsions of the small lens of the brine/SDS/pentanol/dodecane system exhibit properties which are reminiscent of structures with at once water and oil countinuous phases. Microemulsions of the lenticular area of the brine/SDS/pentanol/ hexane system seem to undergo the same structural transitions as microemulsions of systems which present a single monophasic area: water-continuous, bicontinuous and oilcontinuous structures.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Plant and soil 218 (2000), S. 91-101 
    ISSN: 1573-5036
    Keywords: alfalfa ; Aphelenchoides composticola ; Aphelenchus avenae ; barley ; fungi ; host ; nematodes ; N-mineralization ; organic substrates
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract Isolates of Alternaria alternata, Botrytis cinerea, Fusarium oxysporum, Penicillium sp., Rhizoctonia solani, Stemphylium sp., Thielaviopsis basicola, and Verticillium dahliae were cultured on potato–dextrose agar (PDA), barley-sand and alfalfa-sand substrates in petri-dish or in column microcosms. N-mineralization by fungi and fungal-feeding nematodes in combination or fungi alone was assessed. Numbers of Aphelenchus avenae or Aphelenchoides composticola supported by the fungi were measured every 7 days. Times for full colonization of the substrates by fungi ranged from 5 to 15 days. Rhizoctonia solani and B. cinerea on PDA supported the largest A. avenae and A. composticola populations, respectively. Penicillium sp. was a nonhost for A. composticola and A. avenae. Rhizoctonia solani, B. cinerea, V. dahliae, and F. oxysporum supported significantly more nematodes than the other four fungal species. The ranked order of fungi based on the amount of N mineralized in columns free of nematodes was A. alternata (with a rate of 0.052 μg N/g-sand per day), Stemphylium sp., V. dahliae, T. basicola, B. cinerea, F. oxysporum, R. solani, and Penicillium sp. (with a rate of 0.0045 μg N/g-sand perday). The presence of A. avenae resulted in significant increases in mineral N, compared to nematode-free columns colonized by F. oxysporum, R. solani, and T. basicola alone. The presence of A. composticola resulted in significant increases in mineral N, compared to nematode-free columns colonized by A. alternata, B. cinerea, F. oxysporum, and R. solani alone. There was more mineral N incolumns in the presence of A. composticola than A. avenae in most cases.
    Type of Medium: Electronic Resource
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