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  • 1
    ISSN: 1435-1536
    Keywords: Key words Critical micellization concentration (CMC) ; solubility ; degree of counterion binding ; Krafft point ; α-sulfonatomyristic acid methyl ester
    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  For a sodium salt of α-sulfonatomyristic acid methyl ester (14SFNa), one of the α-SFMe series surfactants, critical micellization concentration (CMC), solubility and degree of counterion binding (β) were determined by means of electrocon-ductivity measurements at different temperatures (at every 5 °C) ranging from 15 to 50 °C. The phase diagram of 14SFNa in pure water was constructed from the CMC- and solubility-temperature data, in which the Krafft temperature (critical solution temperature) was found around 0 °C. The changes in the Gibbs energy, ΔG 0 m, enthalpy, ΔH 0 m, and entropy, ΔS 0 m, upon micelle formation as a function of temperature were evaluated taking βvalues into calculation.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1435-1536
    Keywords: Key words Electroconductivity ; differential conductivity ; degree of counterion binding ; dissociation degree of micelles ; α-sulfonato-myristic acid methyl ester
    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  For a sodium salt of α-sulfonatomyristic acid methyl ester (14SFNa), one of the α-SFMe series surfactants, the differential conductivity (∂κ/∂C) T , P vs. square root of concentration (√C) was employed in order to determine not only CMC but also the limiting molar conductance (Λ0) and the molar conductance of micellar species (ΛM). Based on the data of the degree of counterion binding to micelles (β) determined previously at different temperatures ranging 15–50 °C at every 5 °C, the experimental values of the degree of dissociation (ionization) of a micelle (αEX) were calculated by regarding as αEX=1−β. The ratio ΛM/Λ0 corresponding to the ratio of slopes below and above CMC in the curve of specific conductivity (κ) vs. concentration (C), which has been often assumed to be the degree of ionization of micelles (α), was compared with the present αEX. However, the ratio ΛM/Λ0 (=α) was found to have a correlationship with αEX (=1−β) as αEX≈0.40×(ΛM/Λ0), or strictly, αEX=0.40 (ΛM/Λ0)+0.08, indicating that the simple ratio of the slopes below and above CMC in κ vs. C curve is not true for αEX=1−β. On the other hand, the method proposed by Evans gave a value closer to αEX compared with the simple ratio.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1438-2199
    Keywords: Amino acids ; Cysteine metabolism ; Sulfate formation ; Taurine formation ; Hypotaurine ; Sulfur equilibrium
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary l-Cysteine is mainly metabolized to sulfate and taurine through cysteinesulfinate pathway. Alternatively, sulfate is formed in rat liver mitochondria via 3-mercaptopyruvate pathway. Intraperitoneal administration of 5 mmol ofl-cysteine per kg of body weight resulted in the increase in sulfate and taurine (plus hypotaurine) excretion in the 24-h urine, which corresponded to 45.3 and 29.3%, respectively, ofl-cysteine administered. Subcutaneous injection of (aminooxy)acetate, a potent inhibitor of transaminases, together withl-cysteine halved the sulfate excretion and doubled the taurine excretion. In vitro sulfate formation froml-cysteine and froml-cysteinesulfinate in rat liver mitochondria was inhibited by (aminooxy)-acetate. The sulfate-forming activity of liver mitochondria obtained from rats injected with (aminooxy) acetate was also inhibited. These results indicate that the transamination reaction is crucial in sulfate formation and in the regulation of sulfur metabolism. Sulfur equilibrium in mammals was discussed.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1438-2199
    Keywords: Amino acids ; Cysteic acid analysis ; Taurine analysis ; Gas chromatography
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary We have reported preparations and gas chromatographic analyses of volatile derivatives of sulfuric acid and taurine (Masuoka et al., 1988; 1989). By extending these studies, we have developed a method for the gas chromatographic determination of cysteic acid. Cysteic acid was converted to the N-isobutoxycarbonyl derivative by the reaction with isobutyl chloroformate in the presence of sodium hydroxide. After desalting with a cation-exchange column, the derivative was converted to the silver salt by reacting with silver oxide. The resulting silver salt was quantitatively esterified with methyl iodide in the presence of dimethyl sulfate and silver oxide. Dimethyl N-isobutoxy-carbonylcysteate [methyl 2-(N-isobutoxycarbonylamino)-3-(methoxysulfonyl) propanoate] formed was analyzed by gas chromatography. The calibration curve was linear up to 5.0µmol per ml of cysteic acid and the recovery was more than 95%.
    Type of Medium: Electronic Resource
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