A microcomputer compatible method of resolving rate constants in mixed first- and second-order kinetic rate laws

1979 ◽  
Vol 51 (11) ◽  
pp. 1828-1834 ◽  
Author(s):  
Paul B. Kelter ◽  
James D. Carr
Keyword(s):  
Rate Constants ◽  
Second Order ◽  
Order Kinetic ◽  
Kinetic Rate ◽  
Rate Laws

scholarly journals Kinetic and Thermodynamic Studies of Chromium (VI) Sorption by Pure and Carbonized Fluted Pumpkin waste biomass (Telfairia occidentalis Hook F.)

2012 ◽  
Vol 27 ◽  
pp. 11-18
Author(s):  
Timi Tarawou ◽  
Michael Horsfall
Keyword(s):  
Aqueous Solution ◽  
Rate Constants ◽  
Industrial Effluents ◽  
Second Order ◽  
Order Kinetic ◽  
Waste Biomass ◽  
Fluted Pumpkin ◽  
Chromium Vi ◽  
Telfairia Occidentalis ◽  
Pseudo Second Order

The adsorption of chromium (VI) ions from aqueous solution was studied using pure and carbonized fluted pumpkin waste biomass (FPWB). The kinetic data shows a pseudo-first-order mechanism with rate constants of 1.26 × 10-2 and 1.933 × 10-2 mg g-1 min-1 for the pure and carbonized FPWB, respectively. While the pseudo-second-order mechanism has rate constants of 0.93 × 10-1 and 1.33 × 10-1 mg g-1 min-1 for the pure and carbonized waste biomass respectively. The pseudo-second order kinetic model was found to be more suitable for describing the experimental data based on the correlation coefficient values (R2) of 0.9975 and 0.9994 obtained for pure waste biomass (PWB) and carbonized waste biomass (CWB), respectively. The results obtained from this study show that PWB and CWB have very high removal capacity for chromium (VI) from aqueous solution over a range of reaction conditions. Thus, fluted pumpkin waste biomass (Telfairia occidentalis Hook F) is a potential sorbent for the treatment of industrial effluents containing chromium (VI) contaminant.DOI: http://dx.doi.org/10.3126/jncs.v27i1.6436 J. Nepal Chem. Soc., Vol. 27, 2011 11-18Uploaded date: 16 July, 2012

scholarly journals KINETICS OF OZONE REACTIONS WITH ADENINE AND CYTOSINE IN AQUEOUS SOLUTIONS

2020 ◽  
Vol 63 (10) ◽  
pp. 17-22
Author(s):  
Aigul A. Maksyutova ◽  
Elvina R. Khaynasova ◽  
Yuriy S. Zimin
Keyword(s):  
Aqueous Solutions ◽  
Rate Constants ◽  
Correlation Coefficients ◽  
Activation Parameters ◽  
Second Order ◽  
Order Kinetic ◽  
Temperature Dependences ◽  
Ozone Reactivity ◽  
Kinetics Of ◽  
Ozone Reactions

The ultraviolet spectroscopy method has been applied to study the kinetics of the ozone reactions with nitrogenous bases (NB), namely adenine and cytosine in aqueous solutions. At the first research stage, the range of NB working concentrations has been determined. It was found that linear dependences between optical densities and concentrations of nitrogenous bases aqueous solutions are quite reliable, with correlation coefficients r ≥ 0.998, are satisfied up to [NB] = 2.3 ∙ 10–4 mol/l. According to the Bouguer-Lambert-Beer law, adenine and cytosine extinction coefficients in aqueous solutions were determined and subsequently used to calculate their residual concentrations. At the next stage, the kinetics of nitrogenous bases ozonized oxidation was studied with equal initial concentrations of the starting substances ([NB]0 = [О3]0). The results revealed that the kinetic consumption curves of the starting reagents are fairly well linearized (r ≥ 0.996) in the second-order reaction equation coordinates. As found with the bubbling installation, 1 mol of the absorbed ozone falls on 1 mol of the used NB. Thus, the reactions of ozone with adenine and cytosine explicitly proceed according to the second-order kinetic laws (the first – according to О3 and the first – according to NB). The rate constants were calculated by the integral reaction equations, the values of which indicate a higher ozone reactivity in relation to nitrogen bases. The temperature dependences of the second-order rate constants was studied ranging 285-309 K, and the activation parameters (pre-exponential factors and activation energies) of the ozone reactions with adenine and cytosine in aqueous solutions were determined.

Kinetic Study of the Reactions of Some 5-Nitro-2-(4-nitrophenoxy)-3-X-thiophenes with Aniline and 4-Methoxyaniline in Methanol

1999 ◽  
Vol 64 (11) ◽  
pp. 1877-1892 ◽  
Author(s):  
Vincenzo Frenna ◽  
Gabriella Macaluso ◽  
Giovanni Consiglio ◽  
Susanna Guernelli ◽  
Domenico Spinelli
Keyword(s):  
Kinetic Study ◽  
Rate Constants ◽  
Kinetic Constant ◽  
Second Order ◽  
Base Catalysis ◽  
Monotonic Function ◽  
Order Kinetic ◽  
General Acid

The rate constants of the title reactions have been measured at various amine concentrations. The second-order kinetic constant for the amino substitution increases in a hyperbolic way as a function of the nucleophile concentration. The k3Am/k-1 ratio for each catalysed system is not a monotonic function of the X substituent. This result has been rationalized in the framework of the SB-GA (Specific Base-General Acid) mechanism of base catalysis.

Alternate solutions for two particular third order kinetic rate laws

2010 ◽  
Vol 49 (2) ◽  
pp. 328-334 ◽  
Author(s):  
Brian Wesley Williams
Keyword(s):  
Order Kinetic ◽  
Third Order ◽  
Kinetic Rate ◽  
Rate Laws

Inhibition in Purified Systems and in Human Plasma of Chimaeric Plasminogen Activators Consisting of the NH2-Terminal Region of Tissue-Type Plasminogen Activator and the COOH-Terminal Region of UrokinaseType Plasminogen Activator

1988 ◽  
Vol 60 (02) ◽  
pp. 247-250 ◽  
Author(s):  
H R Lijnen ◽  
L Nelles ◽  
B Van Hoef ◽  
F De Cock ◽  
D Collen
Keyword(s):  
Plasminogen Activator ◽  
Rate Constants ◽  
Plasminogen Activators ◽  
Second Order ◽  
Tissue Type ◽  
Single Chain ◽  
Chain Molecules ◽  
Order Rate ◽  
Type Plasminogen Activator ◽  
Urokinase Type Plasminogen Activator

SummaryRecombinant chimaeric molecules between tissue-type plasminogen activator (t-PA) and single chain urokinase-type plasminogen activator (scu-PA) or two chain urokinase-type plasminogen activator (tcu-PA) have intact enzymatic properties of scu-PA or tcu-PA towards natural and synthetic substrates (Nelles et al., J Biol Chem 1987; 262: 10855-10862). In the present study, we have compared the reactivity with inhibitors of both the single chain and two chain variants of recombinant u-PA and two recombinant chimaeric molecules between t-PA and scu-PA (t-PA/u-PA-s: amino acids 1-263 of t-PA and 144-411 of u-PA; t-PA/u-PA-e: amino acids 1-274 of t-PA and 138-411 of u-PA). Incubation with human plasma in the absence of a fibrin clot for 3 h at 37° C at equipotent concentrations (50% clot lysis in 2 h), resulted in significant fibrinogen breakdown (to about 40% of the normal value) for all two chain molecules, but not for their single chain counterparts. Preincubation of the plasminogen activators with plasma for 3 h at 37° C, resulted in complete inhibition of the fibrinolytic potency of the two chain molecules but did not alter the potency of the single chain molecules. Inhibition of the two chain molecules occurred with a t½ of approximately 45 min. The two chain variants were inhibited by the synthetic urokinase inhibitor Glu-Gly-Arg-CH2CCl with apparent second-order rate constants of 8,000-10,000 M−1s−1, by purified α2-antiplasmin with second-order rate constants of about 300 M−1s−1, and by plasminogen activator inhibitor-1 (PAI-1) with second-order rate constants of approximately 2 × 107 M−1s−1.It is concluded that the reactivity of single chain and two chain forms of t-PA/u-PA chimaers with inhibitors is very similar to that of the single and two chain forms of intact u-PA.

Synthesis and Characterization of Chitosan templated Mesoporous Silica: Efficient use of Mesoporous Silica in the removal of Cu(II) from Aqueous Solutions

2016 ◽  
Vol 4 (2) ◽  
pp. 105-112
Author(s):  
Lalchhing puii ◽  
◽  
Seung-Mok Lee ◽  
Diwakar Tiwari ◽  
◽  
...  
Keyword(s):  
Mesoporous Silica ◽  
Aqueous Solutions ◽  
Background Electrolyte ◽  
Second Order ◽  
Order Kinetic ◽  
Sorption Data ◽  
Column Reactor ◽  
Wide Ph Range ◽  
Freundlich Adsorption Isotherm ◽  
Pseudo Second Order

A mesoporous silica was synthesized by annealing (3-Aminopropyl) triethoxysilane grafted chitosan at 800˚C. The mesoporous silica was characterized by the XRD (X-ray diffraction) analysis. The BET specific surface area and pore size of silica was found to be 178.42 m2/g and 4.13 nm. The mesoporous silica was then employed for the efficient remediation of aqueous solutions contaminated with Cu(II) under batch and column reactor operations. The mesoporous silica showed extremely high per cent removal of Cu(II) at wide pH range i.e., pH ~2.0 to 7.0. Relatively a fast uptake of Cu(II) was occurred and high percentage removal was obtained at initial concentrations studied from 1.0 to 15.0 mg/L. The equilibrium state sorption data were utilized for the Langmuir and Freundlich adsorption isotherm studies. Moreover, the effect of an increase in background electrolyte concentrations from 0.0001 to 0.1 mol/L NaNO3 was assessed for the uptake of Cu(II) by mesoporous silica. The equilibrium sorption was achieved within 240 min of contact and the kinetic data is best fitted to the pseudo-second-order and fractal like pseudo-second-order kinetic models. In addition, the mesoporous silica was used for dynamic studies under column reactor operations. The breakthrough curve was then used for the non-linear fitting of the Thomas equation and the loading capacity of the column for Cu(II) was estimated.

Determination of rate constants of redox reactions of second order from current-less potential-time curves by a simplified graphical-numerical method

1983 ◽  
Vol 48 (5) ◽  
pp. 1358-1367 ◽  
Author(s):  
Antonín Tockstein ◽  
František Skopal
Keyword(s):  
Numerical Method ◽  
Explicit Form ◽  
Rate Constant ◽  
Optimization Algorithm ◽  
Rate Constants ◽  
Redox Reactions ◽  
Second Order ◽  
Wide Region ◽  
Recurrent Formula

A method for constructing curves is proposed that are linear in a wide region and from whose slopes it is possible to determine the rate constant, if a parameter, θ, is calculated numerically from a rapidly converging recurrent formula or from its explicit form. The values of rate constants and parameter θ thus simply found are compared with those found by an optimization algorithm on a computer; the deviations do not exceed ±10%.

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