scholarly journals Effect of storage temperature on the decay of catechins and procyanidins in dark chocolate

2017 ◽  
Vol 35 (No. 4) ◽  
pp. 360-366 ◽  
Author(s):  
Pavlović Aleksandra N ◽  
Mrmošanin Jelena M ◽  
Krstić Jovana N ◽  
Mitić Snežana S ◽  
Tošić Snežana B ◽  
...  
Keyword(s):  
Activation Energy ◽  
Reaction Kinetics ◽  
Storage Stability ◽  
Arrhenius Equation ◽  
Storage Temperature ◽  
Order Reaction ◽  
Dark Chocolate ◽  
Total Flavonoids ◽  
Temperature Dependent ◽  
First Order

The storage stability of catechins, procyanidins, and total flavonoids in dark chocolate was investigated. The obtained results showed that the degradation of flavonoids followed first-order reaction kinetics. Temperature-dependent degradation was modelled on the Arrhenius equation. The activation energy for the degradation of dark chocolate flavonoids during storage was 61.2 kJ/mol. During storage, flavonoids degraded more rapidly at 35°C (k = 7.8 × 10<sup>–3</sup>/day) than at 22°C (k = 5.4 × 10<sup>–3</sup>/day) and 4°C (k = 2.2 × 10<sup>–3</sup>/day).

Generation and Dissociation of Iron-Boron Pairs in Silicon

1989 ◽  
Vol 163 ◽  
Author(s):  
Masashi Suezawa ◽  
Koji Sumino
Keyword(s):  
Activation Energy ◽  
Electron Paramagnetic Resonance ◽  
Reaction Kinetics ◽  
Order Reaction ◽  
Migration Energy ◽  
Paramagnetic Resonance ◽  
First Order ◽  
Pair Generation ◽  
Electron Paramagnetic ◽  
Fe Impurity

AbstractThe generation and dissociation processes of Fe-B pairs in Si crystal are investigated by means of the measurements of electron paramagnetic resonance of Si crystals of various B concentrations doped with Fe. Fe-B pairs are generated due to annealing of the crystals at temperatures around 300 K obeying to the first order reaction kinetics. The activation energy for pair generation is determined to be about 0.65 eV which is almost equal to the migration energy of Fe impurity in a Si crystal. Fe-B pairs are found to be dissociated at tempeatures higher than 150°C leading to the precipitation of Fe.

scholarly journals Pyrolysis Reaction Kinetics of Styrofoam Plastic Waste

2021 ◽  
Vol 9 (1) ◽  
pp. 57-62
Author(s):  
Feybi A. G. Kauwo ◽  
I Dewa K. Anom ◽  
John Z. Lombok
Keyword(s):  
Activation Energy ◽  
Reaction Kinetics ◽  
Arrhenius Equation ◽  
Plastic Waste ◽  
Energy Value ◽  
Pyrolysis Reaction ◽  
First Order ◽  
Liquid Smoke ◽  
Reaction Constant ◽  
Kinetics Of

Pyrolysis at the temperature range of 170 °C-237 °C against polystyrene (Styrofoam) type plastic waste is carried out without a catalyst and added a catalyst. The purpose of this research was to study the reaction kinetics of Styrofoam pyrolysis to liquid smoke products. Pyrolysis using a series of tools made of glass to observe the processes that occur in the reactor. The results showed that Styrofoam pyrolysis for liquid smoke products without catalyst and added catalyst took place in the first-order reaction. The kinetics of the pyrolysis reaction without a catalyst to observe the formation of liquid smoke products obtained by the equation of the reaction constant following the Arrhenius equation k = Ae2111.4 / T, with an activation energy value (Ea) of 17.554 x 103 kJ/mol and pyrolysis using a catalyst obtained k = Ae10330/T, with an activation energy value (Ea) of 85.883x103 kJ/mol. Using catalysts during pyrolysis will reduce the temperature so that the reaction will be slow.

scholarly journals GASIFICATION STUDY OF SARAWAK COALS

2017 ◽  
Vol 25 (1) ◽  
pp. 67-72
Author(s):  
Nor Fadzilah Othman ◽  
Mohd Hariffin Bosrooh
Keyword(s):  
Activation Energy ◽  
Kinetic Parameters ◽  
Arrhenius Equation ◽  
Preliminary Investigation ◽  
Reaction Model ◽  
Order Reaction ◽  
Low Rank ◽  
Heating Rates ◽  
First Order ◽  
Air Atmosphere

Thermogravimetry (TG) has been applied in a preliminary investigation, to the gasification of two low rank Sarawak coals. The coal samples, about 10 mg were investigated within the temperature range 30–900°C at different heating rate of 10, 20 and 30°C min-1, under a synthetic air atmosphere for the gasification study. The kinetic parameters were determined using Arrhenius type reaction model assuming a first-order reaction. The reactivity, RT values are fitted with Arrhenius equation at r2 = 0.83 - 0.98 for MP coal, while the RT values for MB coal are fitted with the Arrhenius equation at r2 = 0.99. The activation energy, EA for MP coal are in the range of 3.7 -4.7 kJ mol-1 and for MB coal are 7.6 - 25.6 kJ mol-1 at 3 different heating rates.  

Photocolouration of 2,4,4,6-Tetraaryl-4H-pyrans and Their Heteroanalogues: Importance of Hypervalent Photoisomers

1995 ◽  
Vol 60 (10) ◽  
pp. 1621-1633 ◽  
Author(s):  
Stanislav Böhm ◽  
Mojmír Adamec ◽  
Stanislav Nešpůrek ◽  
Josef Kuthan
Keyword(s):  
Reaction Kinetics ◽  
Absorption Spectra ◽  
Electronic Absorption ◽  
Electronic Absorption Spectra ◽  
Theoretical Data ◽  
Order Reaction ◽  
Bleaching Process ◽  
First Order ◽  
Photodegradation Products ◽  
Hypervalent Molecules

Molecular geometries of 2,4,4,6-tetraphenyl-4H-pyran (Ia), 4,4-(biphenyl-2,2e-diyl)-2,6-diphenyl-4H-pyran (Ib) and their heterocyclic isomers II-V were optimized by the PM3 method and used for the calculation of electronic absorption spectra by the CNDO/S-CI procedure. Comparison of the theoretical data with experimental UV-VIS absorption spectra made possible to select hypervalent molecules IIIa, IIIb, IVa and IVb being responsible for the photocolouration of 4H-pyrans Ia, Ib, while compounds Va, Vb, VI and VII come into account as possible photodegradation products. The bleaching process of the UV illuminated compound Ia is analyzed in terms of dispersive first-order reaction kinetics.

scholarly journals N.M.R. studies of ligand exchange on acetylacetonatotrimethylplatinum(IV)

1975 ◽  
Vol 28 (4) ◽  
pp. 759 ◽  
Author(s):  
NS Ham ◽  
JR Hall ◽  
GA Swile
Keyword(s):  
Activation Energy ◽  
Quantitative Analysis ◽  
Ligand Exchange ◽  
Variable Temperature ◽  
Order Reaction ◽  
First Order Reaction ◽  
First Order ◽  
Cdcl3 Solution ◽  
Made In

A quantitative analysis of the variable-temperature 1H N.M.R. spectra of acetylacetonatotrimethyl-platinum(IV) has been made. In CDCl3 solution the exchange of acetylacetonate ligands is a first-order reaction and proceeds predominantly by dissociation of the dimer into two separated five-coordinate activated complexes. The activation energy is 61.5 � 0.8 kJ mol-1.

scholarly journals Degradation Kinetics of Anthocyanins in Shalgam Beverage

2019 ◽  
Vol 7 (2) ◽  
pp. 282
Author(s):  
Adnan Bozdoğan ◽  
Kurban Yaşar
Keyword(s):  
Activation Energy ◽  
Reaction Kinetics ◽  
Half Life ◽  
Degradation Kinetics ◽  
Production Method ◽  
Order Reaction ◽  
Different Temperatures ◽  
Traditional Production ◽  
Effects Of Temperature ◽  
Kinetics Of

This research was performed to elucidate the effects of temperature on the degradation kinetics of anthocyanins in shalgam beverage. Shalgam beverage was produced according to traditional production method. Then, it was kept at three different temperatures (65°C, 75°C, and 85°C) for 12 hours, and the relevant quantities of anthocyanins were determined thereafter. The research revealed that degradation of the anthocyanins was well described with a 1st-order reaction kinetics model and the R2 values varied in the range of 0.9059-0.9715. Activation energy of the reaction was determined to be 48537 Joule/mole. The half-lives of anthocyanins at 65°C and 75° C, and 85°C were found to be 138.63, 136.72, and 51.57, respectively. Compared the half-life periods at different temperatures, anthocyanins were found to be more resistant at 65°C and 75°C than at 85°C.

Pre-Reduction of Chromite by Thermogravimetric (TG) Analysis

2013 ◽  
Vol 760 ◽  
pp. 23-32
Author(s):  
D.M.A. Khan
Keyword(s):  
Reaction Kinetics ◽  
Order Reaction ◽  
First Order Reaction ◽  
Reduction Mechanism ◽  
Muffle Furnace ◽  
Tg Analysis ◽  
First Order ◽  
Single Pellet ◽  
Reduction Smelting

Thermogravimetric experiments on prereduction of single pellet and multiple pellets were conducted in Muffle furnace at 1500oC. Reduction smelting of Chromite in Fe-C melt in TG setup indicates CR is reduced faster than CG and CB. The reduction mechanism takes the path of first order reaction kinetics. Only 50% Cr metallization could be obtained at 1550oC from the reduction smelting experiments.

On the Chemical Reactivity of the Phytochrome Chromophore in the Pr and Pfr Form

1985 ◽  
Vol 40 (3-4) ◽  
pp. 215-218 ◽  
Author(s):  
Fritz Thümmler ◽  
Peter Eilfeld ◽  
Wolfhart Rüdiger ◽  
Doo-Khil Moon ◽  
Pill-Soon Song
Keyword(s):  
Reaction Kinetics ◽  
Rate Constants ◽  
Chemical Reactivity ◽  
Order Reaction ◽  
First Order Reaction ◽  
Limiting Factor ◽  
Pseudo First Order Reaction ◽  
First Order ◽  
Pseudo First Order ◽  
The Difference

The reactivity of the phytochrome chromophore and related tetrapyrroles towards ozone and tetranitromethane was investigated. Both oxidizing reagents cause bleaching of the main absorp­tion band of the pigment. The rate constants for this bleaching were determined under conditions of pseudo first order reaction kinetics. The rate constants for the reaction with ozone are similar for native phytochrome and for freely accessible tetrapyrroles (biliverdin, small chromopeptides from phytochrome) indicating that accessibility is not the limiting factor for the reaction with ozone. Under a variety of conditions, the Pfr chromophore reacts by about 10% faster than the Pr chromophore. This may reflect the true difference in reactivity. The rate constants for the reaction with tetranitromethane are much larger for biliverdin, bilirubin and small chromopeptides from phytochrome than for native phytochrome. The limiting factor for this reaction in native phytochrome therefore is the accessibility of the chromophore by the reagent. Previous conclusions on the difference in exposure of the tetrapyrrole chromophore in Pr and Pfr are confirmed.

Interactions of hypochlorite ion and humic acid: photolytic and photocatalytic pathways

2001 ◽  
Vol 44 (5) ◽  
pp. 205-210 ◽  
Author(s):  
D. Gonenç ◽  
M. Bekbolet
Keyword(s):  
Humic Acid ◽  
Reaction Kinetics ◽  
Removal Efficiency ◽  
Photocatalytic Oxidation ◽  
Removal Rate ◽  
Order Reaction ◽  
First Order Reaction ◽  
Acid Oxidation ◽  
First Order ◽  
Toc Removal

Photolytic and photocatalytic interactions of hypochlorite ion and humic acid are investigated under various conditions. Humic acid oxidation by aqueous chlorine under dark conditions are expressed in terms of first order reaction kinetics. Upon irradiation (300 nm &lt; λ &lt; 400 nm), photolysis of aqueous chlorine affect the removal efficiency of humic acid via oxidation. TiO2 sensitised photocatalytic oxidation conditions reveal an increase in the TOC removal rate of humic acid in the presence of aqueous chlorine. Under the specified conditions, increasing the photocatalyst loading up to 1.0 mg/mL markedly increase the TOC removal rate.

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