scholarly journals Kinetic studies of metalloporphyrin formation. Part I. Mn(II) with hematoporphyrin

1968 ◽  
Vol 46 (22) ◽  
pp. 3431-3436 ◽  
Author(s):  
Doreen A. Brisbin ◽  
Robert J. Balahura
Keyword(s):  
Acetic Acid ◽  
Glacial Acetic Acid ◽  
Kinetic Studies ◽  
Activation Energies ◽  
Kinetics Of

The kinetics of the formation of Mn(III) hematoporphyrin in glacial acetic acid has been studied spectrophotometrically.On addition of Mn(II) to porphyrin in glacial acetic acid a species which appears to be the monocation immediately is formed and is then converted to Mn(III) hematoporphyrin at a rate suitable for kinetic studies.The rates of reaction were measured at 45, 50, and 55 °C and the activation energies were calculated.

Kinetics of the acid-catalyzed isomerization of phenylbutenes in glacial acetic acid

1972 ◽  
Vol 94 (4) ◽  
pp. 1247-1249 ◽  
Author(s):  
R. S. Schwartz ◽  
H. Yokokawa ◽  
E. W. Graham
Keyword(s):  
Acetic Acid ◽  
Glacial Acetic Acid ◽  
Acid Catalyzed ◽  
Kinetics Of

Kinetics of metalloporphyrin formation in glacial acetic acid

1970 ◽  
Vol 9 (9) ◽  
pp. 2034-2037 ◽  
Author(s):  
D. James Kingham ◽  
Doreen A. Brisbin
Keyword(s):  
Acetic Acid ◽  
Glacial Acetic Acid ◽  
Kinetics Of

scholarly journals Application of the Shrinking-Core Models for Determination of Dissolution Kinetics of Mn and Zn from Spent Zinc–Carbon Battery Powder in Organic Acid Solution

2019 ◽  
Vol 27 (1) ◽  
pp. 99-109 ◽  
Author(s):  
Tevfik Agacayak ◽  
Hasan Ali Taner
Keyword(s):  
Acetic Acid ◽  
Acid Solution ◽  
Acetic Acid Solution ◽  
Dissolution Kinetics ◽  
Kinetic Studies ◽  
Product Layer ◽  
Different Temperatures ◽  
Shrinking Core ◽  
Kinetics Of Dissolution ◽  
Kinetics Of

Abstract In this study, dissolution kinetics of manganese and zinc from spent zinc–carbon batteries in acetic acid solution was investigated. To determine the kinetics of dissolution of manganese and zinc, shrinking core model was applied to dissolution recoveries obtained at different temperatures. As a result of kinetic studies, it was determined that manganese and zinc were dissolved in acetic acid solution by diffusion from product layer and then activation energies (Ea) were calculated.

scholarly journals THE PHOTOINITIATED ADDITION OF MERCAPTANS TO OLEFINS: III. THE KINETICS OF THE ADDITION OF THIOPHENOL TO STYRENE AND TO 1-OCTENE

1957 ◽  
Vol 35 (7) ◽  
pp. 723-733 ◽  
Author(s):  
R. H. Pallen ◽  
C. Sivertz
Keyword(s):  
Free Radical ◽  
Rate Constants ◽  
Chain Transfer ◽  
Kinetic Studies ◽  
Activation Energies ◽  
Reverse Reaction ◽  
Kinetics Of

Kinetic studies were made of the free radical photoinitiated addition of thiophenol to 1-octene and to styrene in the absence of oxygen. In addition to the usual attack, chain transfer, and termination steps, it is found that a reverse reaction accompanies the attack step, [Formula: see text] The rate constants for the thiophenol–styrene reaction were calculated to be [Formula: see text]kt = 2 × 107 liters.moles−1sec.−1. The over-all activation energies for the two reactions were found to be E (1-octene) = 1.2 kcal., E (styrene) = 2.4 kcal.; suggestions are submitted as to why these activation energies are so low. These reactions are compared with n-butyl mercaptan – olefin reactions.

scholarly journals Structural and Gasification Kinetic Studies on Co-pyrolysis Chars of Coal and Biomass

2021 ◽  
Author(s):  
Lang Liu ◽  
Jingsong Zeng ◽  
Qingrui Jiao ◽  
Shan Ren ◽  
Jian Yang ◽  
...  
Keyword(s):  
Thermogravimetric Analysis ◽  
Porous Structure ◽  
Kinetic Studies ◽  
Activation Energies ◽  
Biomass Composition ◽  
Pore Model ◽  
Gasification Reactivity ◽  
Char Gasification ◽  
The Relationship ◽  
Kinetics Of

Abstract In the present study, the CO2 gasification behaviours of the co-pyrolysis chars with coal and biomass as feedstock were investigated using isothermal thermogravimetric analysis (TGA) at 950–1150 °C. The TGA results demonstrated that the char gasification reactivity was improved at higher biomass composition. In addition, the char characteristics results evaluation revealed that biomass promoted the development of a porous structure and inhibited the formation of graphite-like carbon during the co-pyrolysis of coal and biomass. Moreover, an extended random pore model (eRPM) was proposed to define the char gasification kinetics of coal and biomass. It was found that the activation energies of chars decreased with increasing biomass composition. Lastly, the relationship between the gasification reactivity and char characteristics was evaluated.

Synthesis and Caracterization of some New 1H-3-aryl-7-etoxycarbonyl-6-methyl-pyrazolo[5,1-c][1,2,4]triazoles

2008 ◽  
Vol 59 (1) ◽  
pp. 41-44
Author(s):  
Maria-Daniela Sofei ◽  
Maria Ilici ◽  
Valentin Badea ◽  
Carol Csunderlik ◽  
Vasile-Nicolae Bercean
Keyword(s):  
Mass Spectrometry ◽  
Acetic Acid ◽  
Nmr Spectroscopy ◽  
Sodium Acetate ◽  
Glacial Acetic Acid ◽  
Ir And Nmr Spectroscopy

The synthesis of 1H-3-aryl-7-ethoxycarbonyl-6-methyl-pyrazolo[5,1-c][1,2,4]triazoles (2) was carried out by cyclization of 1H-5-arylidenehydrazino-4-ethoxycarbonyl-3-methyl-pyrazoles (1) in the presence of bromine using glacial acetic acid as solvent and sodium acetate as base. The new nine obtained compounds were characterized by IR and NMR spectroscopy and mass spectrometry.

Coordination state of cobalt(II) ions in solution and on a sulphonated organic polymer

1979 ◽  
Vol 44 (8) ◽  
pp. 2330-2337 ◽  
Author(s):  
Jindřiška Maternová ◽  
Anastas A. Andreev ◽  
Dimitrii M. Shopov ◽  
Karel Setínek
Keyword(s):  
Acetic Acid ◽  
Coordination Sphere ◽  
Glacial Acetic Acid ◽  
Organic Polymer ◽  
Octahedral Complex ◽  
Coordination State ◽  
Tetrahedral Symmetry ◽  
Liquid Acid ◽  
Homogeneous Phase ◽  
Bromide Ion

It was found spectroscopically that cobalt(II) acetate dissolved in glacial acetic acid forms the octahedral complex [Co(OAc)2(HOAc)4] which in the presence of bromide ions gives the octahedral [Co(OAc)Br(HOAc)4] and tetrahedral bromo(acetate)cobalt(II) complexes with the higher number of Br- ions. When attached to an organic polymer cobalt(II) ions are bonded in the form of octahedral [Co(H2O)6]2+ cations which form with acetic acid similar complexes as in homogeneous phase and are able to coordinate one bromide ion. Drying the copolymer possessing octahedral hexaaquocobalt(II) cations leads to tetrahedral aquocomplexes which are solvated by gaseous acetic acid and converted into the acetate complexes with the liquid acid. The latter contain the acid in the inner coordination sphere and have tetrahedral symmetry.

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