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  • Antagonists  (2)
  • Chemical Engineering  (2)
  • Physics  (2)
  • buffalo  (2)
  • 1
    ISSN: 1432-0789
    Keywords: Macrophomina phaseolina ; Antagonists ; Germination ; Agglutination ; Pseudomonas fluorescence ; Trichoderma harzianum
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Geosciences , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract The colonization of Macrophomina phaseolina sclerotia by microbial parasites was evaluated in unsterilized field soil at different levels of soil moisture (0,-5, and-10 kPa) and temperature (20, 30, and 40°C). The maximum colonization of sclerotia was recorded in soil held at-5 or-10 kPa at 30–40°C. Trichoderma harzianum isolate 25–92 and Pseudomonas fluorescens isolate 4–92 were recorded as potential sclerotial parasites, and they significantly (P=0.05) reduced the germination of sclerotia by 60–63%. Cells of P. fluorescens and buffer-washed conidia of T. harzianum were completely agglutinated at 28°C with crude agglutinin of M. phaseolina. The ability of different antagonists to parasitize the sclerotia were correlated with the agglutination ability of the antagonists.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-0789
    Keywords: Key wordsMacrophomina phaseolina ; Antagonists ; Germination ; Agglutination ; Pseudomonas fluorescence ; Trichoderma harzianum
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Geosciences , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract The colonization of Macrophomina phaseolina sclerotia by microbial parasites was evaluated in unsterilized field soil at different levels of soil moisture (0, –5, and –10 kPa) and temperature (20, 30, and 40°C). The maximum colonization of sclerotia was recorded in soil held at –5 or –10 kPa at 30–40°C. Trichoderma harzianum isolate 25–92 and Pseudomonas fluorescens isolate 4-92 were recorded as potential sclerotial parasites, and they significantly (P=0.05) reduced the germination of sclerotia by 60–63%. Cells of P. fluorescens and buffer-washed conidia of T. harzianum were completely agglutinated at 28°C with crude agglutinin of M. phaseolina. The ability of different antagonists to parasitize the sclerotia were correlated with the agglutination ability of the antagonists.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1573-7446
    Keywords: buffalo ; disposition ; dose ; kanamycin ; pharmacokinetics ; serum ; urine
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The disposition kinetics and appropriate dosage regimen for kanamycin were investigated in buffalo calves following a single intravenous dose of 10 mg/kg body weight. The distribution and elimination half-lives were 0.12±0.01 h and 1.94±0.11 h, respectively. The apparent volume of distribution and total body clearance were 0.2±0.01 L/kg and 92.9±3.69 ml/kg/h, respectively. About 74% of the administered dose was excreted in urine in 24 h. A suitable dosage regimen for the intravenous administration of kanamycin was also calculated.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 34 (1994), S. 528-531 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    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: Terpolymerization was investigated by dilatometry for zincacrylate (ZnA2), acrylonitrile (AN), and styrene (St), radically initiated by a As2S3-styrene complex (I) in dimethyl sulphoxide (DMSO), at 90 ± 0.1°C for 1 h under inert atmosphere. The system follows non-ideal kinetics, due to primary radical termination as well as a degradative chain transfer reaction. The kinetic expression for the system is Rpα(I)0.27 (St)0.31 (AN) 0.22[ZnA2]0.12. The value for the activation energy and kp2/kt are 55 kJ mol-1 and 1.87 × 10-7 1 mol-1 s-1 respectively. The terpolymer has been characterized by IR and NMR spectroscopy. The thermal stability and solubility of the terpolymer have also been studied.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1573-7446
    Keywords: buffalo ; cephalexin ; pharmacokinetics ; treatment
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 31 (1991), S. 567-570 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    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: Radical polymerization of methacrylic acid (MAA) and acrylonitrile (AN) in the presence of p-nitrobenzyl triphenyl phosphonium ylide (p-NBTPy) in dimethyl sulphoxide at 65 ± 0.1°C under inert atmosphere was investigated by dilatometry. The ylide failed to initiate the polymerization, but significantly accelerated the rate of polymerization. An interesting feature is that the average polymer molecular weight (M̄v) is a direct function of [p-NBTPy]. The radical polymerization of MAA follows ideal kinetics since calculated monomer and initiator (AIBN) exponents are unity and 0.5, respectively. However, the AN system follows non-ideal kinetics due primarily to radical termination and transfer reactions. The energy of activation, in the presence of p-NBTPy, is low. The accelerating effect of p-NBTPy has been attributed to decreased termination because the ylide did not affect the rate of decomposition of AIBN, as well as form a complex with monomer(s).
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 22 (1984), S. 1875-1882 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The ylide 4-picolinium, p-chloro phenacylide-initiated thermal polymerization of ethyl methacrylate (EMA) was studied. 4-Picolinium p-chloro phenacylide induces the thermal polymerization of ethyl methacrylate at 65°C. The rate of polymerization (Rp) rose as the initiator concentration increased from 2 × 10-3 to 4 × 10-3 M and the initiating exponent was computed as 1.9. The Rp decreased as the concentration of ylide increased from 6 × 10-2 to 1M. The greater initiator concentration also affected the molecular weight inversely. The polymerization was carried out at different temperatures and the overall activation energy was computed as 4.08 Kcal/mol. Polymerization was inhibited in the presence of hydroquinone as a radical scavenger. Kinetic studies and other data show that the overall polymerization takes place in a radical mechanism. The various kinetic parameters, such as the rate and average degree of polymerization, molecular weight, and energy of activation of the present system, were evaluated.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 23 (1985), S. 2405-2411 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The thermal polymerization of methyl methacrylate [MMA] was carried out using ylide (4-picolinium 4-chloro phenacyl methylide) as an initiator. The rate of polymerization (Rp) increases with increasing monomer and initiator concentrations; The exponent value has been computed to be 1 ± 0.02 and 0.5, respectively. The reaction was carried out at four different temperatures and the overall activation energy has been computed to be 16.01 kcal/mol. The polymerization was inhibited in the presence of hydroquinone as a radical scavanger. Kinetic studies indicates that the overall polymerization takes place by a radical mechanism.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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