Absolute Light Scattering Calibration of the Stopped-Flow Spectrophotometer with Application to the Kinetics of Formation of Monodispersed Colloidal Hematite

1987 ◽  
Vol 41 (3) ◽  
pp. 402-407 ◽  
Author(s):  
Wan Peter Hsu ◽  
Ramesh C. Patel ◽  
Egon Matijevic

A calibration method based on absolute intensities of scattered light from colloidal silica was developed to standardize the stopped-flow temperature jump spectrophotometer (SFTJ). The need for such calibration was exemplified by the study of the temperature effect on the Rayleigh ratio changes during the formation of solid iron (hydrous) oxides.

1974 ◽  
Vol 52 (1) ◽  
pp. 8-17 ◽  
Author(s):  
Leong Huat Gan ◽  
Albert Richard Norris

Equilibrium constants for the formation of 1:1 cyanide ion σ-complexes with 1,3,5-trinitrobenzene, 2,4,6-trinitroanisole, and 2,4,6-trinitrotoluene have been determined spectrophotometrically over a range of temperatures. Standard enthalpy (ΔH0) and entropy (ΔS0) changes associated with each reaction have been evaluated. The kinetics of formation of the σ-complexes have been investigated by means of a stopped-flow technique and the activation parameters characterizing the formation of each complex have been determined. Evidence is presented which indicates the cyanide ion – 2,4,6-trinitroanisole σ-complex formed in isopropanol contains the cyanide ion bonded exclusively at the C-3 position.


1972 ◽  
Vol 50 (19) ◽  
pp. 3117-3123 ◽  
Author(s):  
G. Boivin ◽  
M. Zador

The kinetics of the formation and dissociation of Cu(II) complexes of adenosine have been determined in acidic and basic medium. In acidic medium, the complex is formed between the Cu(II) and the adenine base and the kinetic parameters have been obtained in this case using a temperature jump method. In basic medium, only the dissociation of the complexes could be studied by a stopped-flow method, by addition of EDTA or strong acid solutions. In these complexes, Cu(II) is bridged with ribose hydroxyls. Finally, D-ribose has also been studied for comparison in the same conditions. The mechanism of these reactions is discussed.


1966 ◽  
Vol 37 (6) ◽  
pp. 746-750 ◽  
Author(s):  
James E. Erman ◽  
Gordon G. Hammes

1972 ◽  
Vol 50 (23) ◽  
pp. 3861-3865 ◽  
Author(s):  
M. L. Sanduja ◽  
W. MacF. Smith

The kinetics of formation of the monophenanthroline complex of nickel(II) in ethanol has been studied using stopped-flow methods over the temperature range 7 to 35 °C. Tetrabutyl ammonium perchlorale in concentration 0.044 M does not affect the rate appreciably, sodium perchlorate at the same concentration depresses the rate significantly. Most measurements were made in the absence of electrolytes other than nickel perchlorate and a trace of perchloric acid. The second order rate constant is not significantly dependent on the nickel(II) concentration over a four-fold change in value indicating that the concentration of encounter pairs is small relative to the concentration of the free reactants. The rate constant at 25 °C (31 × 103 M−1 s−1)is consistent with a dissociative interchange mechanism and the rate constant for ethanol exchange on nickel. However, the value of ΔH≠ for the overall reaction (15.9 ± 1.0 kcal mol−1) is about 5 kcal mol−1 higher than that reported for ethanol exchange.


1981 ◽  
Vol 117 (1) ◽  
pp. 164-169 ◽  
Author(s):  
A.S. Verkman ◽  
James A. Dix ◽  
A.A. Pandiscio

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