scholarly journals Influence of impurities of the transitional metals Fe, Ni, and Co on the hydrolysis kinetics of BH− 4 ions in alkaline solutions

2021 ◽  
Vol 21 (3) ◽  
pp. 164-170
Author(s):  
Irina M. Gamayunova ◽  
Keyword(s):  
Activation Energy ◽  
Catalytic Effect ◽  
Arrhenius Equation ◽  
Alkaline Solutions ◽  
Hydrolysis Kinetics ◽  
Transitional Metals ◽  
Hydrolytic Process ◽  
Kinetics Of ◽  
Hydrolysis Of ◽  
Influence Of Impurities

The influence of small amounts of the Fe, Co, and Ni impurities on the spontaneous hydrolytic process of borohydride was studied within a temperature range of 60–100°C. The object under study was a simulated solution containing 9.53 M of OH− ions and 0.14 M of BH− 4 ions, used as a fuel for borohydride fuel cells. The rate constant k of borohydride hydrolysis for a small amount of impurities at different temperature was estimated. The lowest non-accelerating concentrations of the impurities were established (∼10 ppm for iron; ∼1 ppm for cobalt). The strongest accelerating effect on the hydrolysis of BH− 4 ions was rendered by nickel impurities: self-hydrolysis was accelerated by 1.2 times for 1 ppm Ni. The ambiguous trend of the kinetic curves does not allow to accurately estimate the activation energy; however, the increased temperature enhances the catalytic effect of hydrolysis acceleration according to Arrhenius’ equation.

Hydrolysis Kinetics of Cornstalk in Formic Acid Solution

2012 ◽  
Vol 535-537 ◽  
pp. 2438-2441
Author(s):  
Jun Ping Zhuang ◽  
Xue Ping Li
Keyword(s):  
Activation Energy ◽  
Acid Solution ◽  
Formic Acid ◽  
Wood Fiber ◽  
Hydrolysis Kinetics ◽  
Practical Applications ◽  
And Performance ◽  
Promising Source ◽  
Kinetics Of ◽  
Hydrolysis Of

Cornstalk, among the agricultural residues and other non-wood fiber, is a more promising source of lignocellulosic materials for bioethanol production. Pretreatment is an essential step in the enzymatic hydrolysis of biomass and subsequent production of bioethanol. Kinetic models can have practical applications for the optimization of the process and performance analysis, or economic estimations, so investigate the cornstalk hydrolysis kinetics is necessary. In this paper, effects of temperature and time on cornstalk hydrolysis in saturated formic acid with 4% hydrochloric acid solution reaction kinetics have been investigated. The results showed that the hydrolysis velocities of cornstalk were 0.021 h−1 at 60 °C, 0.0302 h−1 at 65 °C and 0.060 h−1 at 70 °C, the degradation velocities of glucose were 0.061 h−1 at 60 °C, 0.0845 h−1 at 65 °C, and 0.24 h−1 at 70 °C, the activation energy of cornstalk hydrolysis was 99.60 kJ/mol, and the activation energy of glucose degradation was130.94 kJ/mol.

scholarly journals Kinetic Analysis of the Hydrolysis of Pentose-1-Phosphates Through Apparent Nucleoside Phosphorolysis Equilibrium Shifts

2020 ◽  
Author(s):  
Felix Kaspar ◽  
Peter Neubauer ◽  
Anke Kurreck
Keyword(s):  
Kinetic Analysis ◽  
Hydrolysis Kinetics ◽  
Equilibrium Thermodynamics ◽  
Apparent Increase ◽  
Equilibrium Conversion ◽  
Sugar Phosphates ◽  
Kinetics Of ◽  
Hydrolysis Of

<div>Ask what an equilibrium can do for you:</div><div>Hydrolysis of pentose-1-phosphates leads to an apparent increase of the equilibrium conversion in nucleoside phosphorolysis reactions. This information can be leveraged via equilibrium thermodynamics to determine the hydrolysis kinetics of in situ generated sugar phosphates, which are known to be elusive and difficult to quantify.<br></div>

scholarly journals Phenylcarbamic acid derivatives with integrated n-phenylpiperazine moiety in the structure – kinetics of alkaline hydrolysis study / Deriváty kyseliny fenylkarbámovej s integrovanou n-fenylpiperazínovou zložkou v štruktúre – štúdium kinetiky alkalickej hydrolýzy

2015 ◽  
Vol 62 (2) ◽  
pp. 38-42
Author(s):  
Stankovičová M. ◽  
Miháliková V. ◽  
Mezovský Ľ. ◽  
Lašáková A. ◽  
Medlenová V. ◽  
...  
Keyword(s):  
Alkaline Hydrolysis ◽  
Phenyl Ring ◽  
Arrhenius Equation ◽  
Sodium Hydroxide Solution ◽  
Antimycobacterial Activity ◽  
First Order ◽  
Rate Of Hydrolysis ◽  
Pseudo First Order ◽  
Kinetics Of ◽  
Hydrolysis Of

AbstractIn present work, we have studied kinetics of alkaline hydrolysis of 14 compounds, which are phenylcarbamic acid derivatives with integrated N-phenylpiperazine moiety in the structure. The compounds possessed moderate antiarrhythmic and antimycobacterial activity. Their hydrolysis was carried out in an aqueous medium ethanol sodium hydroxide solution. The course of the hydrolysis was observed spectrophotometrically in visible as well as in ultraviolet regions. The pseudo-first order rate constants were calculated at several temperatures. The values of the activation energy EAwere determined by the Arrhenius equation. The rate of hydrolysis of the compounds under the study increase with the increase in temperature and it has been differentiated according to the substitution of N-phenylpiperazine as well as to the alkoxy substitution on phenyl ring.

Kinetics of Cyanate Decomposition in Alkaline Solutions of High Ionic Strength:  The Catalytic Effect of Bicarbonate

2004 ◽  
Vol 43 (16) ◽  
pp. 4815-4821 ◽  
Author(s):  
Nikolai DeMartini ◽  
Dmitry Yu. Murzin ◽  
Mikael Forssén ◽  
Mikko Hupa
Keyword(s):  
Ionic Strength ◽  
Catalytic Effect ◽  
High Ionic Strength ◽  
Alkaline Solutions ◽  
Kinetics Of

THE NON-ENZYMATIC HYDROLYSIS OF ADENOSINE DIPHOSPHATE

1957 ◽  
Vol 35 (12) ◽  
pp. 1496-1503 ◽  
Author(s):  
K. A. Holbrook ◽  
Ludovic Ouellet
Keyword(s):  
Activation Energy ◽  
Aqueous Solution ◽  
Enzymatic Hydrolysis ◽  
Inorganic Phosphate ◽  
Adenosine Diphosphate ◽  
Hydrogen Ions ◽  
Kcal Mole ◽  
First Order ◽  
Kinetics Of ◽  
Hydrolysis Of

The kinetics of the non-enzymatic hydrolysis of adenosine diphosphate in aqueous solution have been studied at pH 3.5 to 10.5 and temperatures from 80° to 95 °C. The reaction has been followed by measuring colorimetrically the inorganic phosphate liberated according to the over-all reaction[Formula: see text]The reaction has been found to be first order with respect to ADP concentration and to be catalyzed by hydrogen ions. From rate studies at pH 8.0 an activation energy of 24.2 kcal./mole was derived. A mechanism is proposed to account for the observed facts and the mechanism for the hydrolysis of adenosine triphosphate is also discussed.

Research on Kinetics of Hydrolysis Preparation of Micro-Molecular Dextran

2013 ◽  
Vol 748 ◽  
pp. 295-298
Author(s):  
Shu Qiong Liao ◽  
Xiao Yu Peng ◽  
Xue Wang Zhang ◽  
Ke Lin Huang ◽  
Ben Wang ◽  
...  
Keyword(s):  
Activation Energy ◽  
Molecular Weight ◽  
Kinetics Equation ◽  
Temperature Range ◽  
Kinetics Of Hydrolysis ◽  
Kinetics Of ◽  
Hydrolysis Of

Micro-molecular dextran was prepared in sub-critical water and sub-critical Water/CO2by hydrolysis of dextran20. The obtained products were mainly characterized by GPC. The kinetics of hydrolysis of dextran20 has been studied in the temperature range of 423.15K-463.15K. It was found that the level of dextran20 hydrolysis in sub-critical water and sub-critical water/CO2was first level kinetics equation. The activation energy was also calculated. The results demonstrated that the molecular weight of micro-molecular dextran could be controlled.

Kinetics of aquation and base hydrolysis of the macrocyclic complex trans-Bromo(N-meso-5,12-dimethyl-1,4,8,11-tetraazacyclotetradeca-4,11-diene)nitro-cobalt(III) perchlorate

1976 ◽  
Vol 29 (10) ◽  
pp. 2319 ◽  
Author(s):  
GA Lawrance ◽  
RW Hay
Keyword(s):  
Activation Parameters ◽  
Macrocyclic Complex ◽  
Base Hydrolysis ◽  
Hydrolysis Kinetics ◽  
Rate Expression ◽  
Entropy Of Activation ◽  
Ph Range ◽  
Kinetics Of ◽  
Hydrolysis Of

The macrocyclic complex trans-[Co(dtcd)(NO2)Br] [ClO4] (dtcd = 5,12-dimethyl-l,4,8,1l-tetraaza-cyclotetradeca-4,ll-diene) has been prepared and its hydrolysis kinetics investigated. At 25�C and 0.1 M HN03 the aquation occurs with kaq = 6.2 x 10-3 s-1 to give the trans-Co(dtcd)(NO2)- (OH2)]2+ cation. The activation parameters at 298 K are ΔH? = 75.0 kJ mol-1 and ΔS? = -35.6 J K-1 mol-1. Hydrolysis of the bromide in the pH range 7.5-8.8 follows the rate expression kobs = kaq + kOH[OH-]. At 25�C (I = 0.1 M, NaClO4) kOH = 1.21 x 103 1. mol-1 s-1 with the activation parameters for base hydrolysis being ΔH? = 74.2 kJ mol-1 and ΔS? = +63.2 J K-1 mol-1 at 298 K. Aquation and base hydrolysis of the bromo complex at 25�C occur at rates 14 and 5 times faster respectively than those previously reported for the analogous trans-[Co(dtcd)(NO2)Cl]+ complex, the acceleration being due to a more favourable entropy of activation in each case.

THE NON-ENZYMATIC HYDROLYSIS OF p-NITROPHENYL PHOSPHATE

1958 ◽  
Vol 36 (4) ◽  
pp. 686-690 ◽  
Author(s):  
K. A. Holbrook ◽  
Ludovic Ouellet
Keyword(s):  
Activation Energy ◽  
Enzymatic Hydrolysis ◽  
Ionic Species ◽  
Kcal Mole ◽  
First Order ◽  
Colorimetric Measurement ◽  
Nitrophenyl Phosphate ◽  
Ph Range ◽  
Kinetics Of ◽  
Hydrolysis Of

The kinetics of the non-enzymatic hydrolysis of p-nitrophenyl phosphate have been studied in aqueous solution in the pH range 2.6 to 9.0 and at temperatures from 68.0°to 82.0 °C. The reaction has been followed by colorimetric measurement of the nitrophenol produced by the reaction[Formula: see text]The reaction is first order with respect to p-nitrophenyl phosphate and has an activation energy of 26.0 kcal./mole at pH 2.6. An explanation has been proposed in terms of the different rates of hydrolysis of the various ionic species of the ester present in solution.

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