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  • 42.55.Px  (1)
  • Ion-pair chromatography  (1)
  • Ion-pair reagent  (1)
  • 1
    ISSN: 1432-0649
    Keywords: 42.55.Px ; 42.65.-k
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract We describe the generation of femtosecond high power optical pulses using hybrid passive-active mode-locking techniques. Angle stripe geometry GaAs/AlGaAs semiconductor laser amplifiers are employed in an external cavity including prisms and a stagger-tuned quantum-well saturable absorber. An identical amplifier also serves as an optical power amplifier in a stretched pulse amplification and recompression sequence. After amplification and pulse compression this laser system produces 200 fs, 160 W peak power pulses. We discuss and extend our theory, and supporting phenomenological models, of picosecond and subpicosecond optical pulse amplification in semiconductor laser amplifiers which has been successful in calculating measured spectra and time-resolved dynamics in our amplifiers. We have refined the theory to include a phenomenological model of spectral hole-burning for finite intraband thermalization time. Our calculations are consistent with an intra-band time of approximately 60 fs. This theory of large signal subpicosecond pulse amplification will be an essential tool for understanding the mode-locking dynamics of semiconductor lasers and for analysis of high speed multiple wave-length optical signal processing and transmission devices and systems based on semiconductor laser amplifiers.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Chromatographia 35 (1993), S. 390-394 
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Electrostatic model ; Ion-pair reagent ; Organic modifier ; Prediction of k′ values
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The capacity factors of phenylamine and naphthylamine sulphonic acids in reversed-phase, ion-pair liquid chromatography (RP-IPC) were measured. The combined effects of organic modifier (Cb) and ion-pair reagent concentration (Cp) on retention follow an equation based on the electrostatic model: $$\ln k' = a + b lnC_p + cC_b $$ the experimental value of b correlates well with the value of 0.5 z (z=charge on analyte ion) predicted for mono and divalent ions. The measured value of b is, however, lower than that predicted for trivalent ions, which may be due to the effective number of charges being less than the apparent number. The absolute values of a and c are much larger than those in RP-HPLC in the absence of an ion-pair reagent, quantitative correlation of a and c with retention values in RP-HPLC and solute charges has been observed and a good linear relationship between a and c has been obtained, strongly supporting the validity of the electrostatic retention model. A critical value, R, at which the negative effect of methanol on retention is equal to the positive effect of the ion-pair reagent (TBAI) has been proposed. The critical values obtained are related to the behaviour of the solute, the ion-pair reagent and the stationary and mobile phases, and lies between −0.04 and −0.065 in most cases, which means that the increase by exp times (=2.718×) the ion-pair concentration the original is equivalent to a decrease of 0.04–0.065 in volume fraction of methanol
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1612-1112
    Keywords: Ion-pair chromatography ; Solute charges ; Solute hydrophobicity ; Quantitative correlation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The Logarithm of capacity factor in RP-HPLC and solute charges have been selected as descriptors of solute hydrophobicity and electrostatic interaction respectively. It has been observed that the logarithm of capacity factors (ln k ip ′ ) for a solute with one, two and three negative charges in RP-IPC can be well correlated with the logarithms of capacity factors (ln kR p ′ ) in RP-HPLC and solute charges (ne). Both the solute hydrophobicity and solute charges with opposite sign to those of the ion-pair reagent made a positive contribution to retention in RP-IPC. The logarithm of capacity factor linearly decreases with organic modifier concentration (Cb) and the logarithm of the inorganic salt concentration (lnCs). The intercept (ln k ip ′ , A) and slope (cip,B) values of a linear relationship between ln kR p ′ vs. Cb and ln k ip ′ vs. ln C5 also can be well correlated with ln kR p ′ and ne. The solute hydrophobicity and solute charges also made a positive contribution to the parameters ln k ip w and A, but a negative contribution to parameter cip. The parameter B, however is mainly determined by the solute charges.
    Type of Medium: Electronic Resource
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