RELATIONSHIP BETWEEN PEAK HEIGHT,PEAK TEMPERATURE AND ACTIVATION ENERGY OF DESORPTION IN TPD SPECTRUM OF FIRST ORDER DESORPTION KINETICS

1987 ◽  
Vol 3 (03) ◽  
pp. 313-320
Author(s):  
Yang Shangrun ◽  
Keyword(s):  
Activation Energy ◽  
Peak Height ◽  
Peak Temperature ◽  
Desorption Kinetics ◽  
First Order ◽  
Activation Energy Of Desorption

scholarly journals DESORPSI β-KAROTEN MINYAK KELAPA SAWIT (CRUDE PALM OIL) DARI KARBON AKTIF MENGGUNAKAN ISOPROPANOL

2017 ◽  
Vol 5 (4) ◽  
pp. 1-7
Author(s):  
Nurul Aini ◽  
Olyvia Putri Wardhani ◽  
Iriany
Keyword(s):  
Activation Energy ◽  
Activated Carbon ◽  
Isopropyl Alcohol ◽  
Desorption Kinetics ◽  
Crude Palm Oil ◽  
Desorption Process ◽  
First Order ◽  
Constant Rate ◽  
Β Carotene ◽  
Main Material

The aim of the research is to study the ability of isopropyl alcohol in the desorption of β-carotene and to obtain kinetic model and desorption isoterm which is suitable in β-carotene desorption. The main material used were isopropyl alcohol and activated carbon containing β-carotene. The variabels used in this research are desorption temperature,  activated carbon concentration  and parameter observed is concentration of β-carotene in isopropyl alcohol. In the desorption process, activated carbon which adsorp β-carotene was soaked in isopropyl alcohol. To review the desorption kinetics, this research was carried out in various temperature such as 40 oC, 50 oC, and 60 oC. In desorption isoterm process is, various mass of activated carbon was used. Desorption process will be analyzed at spesified time. This research used the first order of desorption kinetics model. The desorption constant rate obtained for 40 oC, 50 oC, and 60 oC are 0,013, 0,014, and 0,036 minute-1 with activation energy is 0,226 kkal/mol. The maximum desorption percentage obtain is 41,94 %. The desorption isoterm model which fit with the β-carotene desorption was Langmuir isoterm model with constanta value 1,2077 L/mg and -0,2218.

Comparison of H2 Desorption Kinetics from Si(111)7×7 and Si(100)2×l

1990 ◽  
Vol 204 ◽  
Author(s):  
M. L. Wise ◽  
B. G. Koehler ◽  
P. Gupta ◽  
P. A. Coon ◽  
S. M. George
Keyword(s):  
Activation Energy ◽  
Preexponential Factor ◽  
Desorption Kinetics ◽  
Bond Energies ◽  
First Order ◽  
First Order Kinetics ◽  
Upper Limits ◽  
Desorption Activation Energy ◽  
Temperature Programmed ◽  
Kinetics Of

ABSTRACTThe desorption kinetics of hydrogen from the β1 H2 -TPD state on Si(111)7×7 and Si(100)2×l were studied using laser-induced thermal desorption (LITD) and temperature programmed desorption (TPD) techniques. Isothermal LITD studies of H2 desorption from Si(111)7×7 revealed second-order kinetics with a desorption activation energy of Ed = 62 ±4 kcal/mol and a preexponential factor of Vd = 92 ±10 cm2 /s. In contrast, H2 desorption from Si(100)2×l revealed first-order kinetics with an activation energy of Ed = 58 ±2 kcal/mol and a preexponential factor of Vd = 5.5 ±0.5 × 1015 s−1. The desorption kinetics yield similar upper limits for the Si-H bond energies but different desorption mechanisms on Si(lll)7×7 and Si(100)2×l.

Vulcanization of Elastomers. 23. The Chemical Kinetics of Vulcanization Reactions and The Physical Properties of The Vulcanizates. I

1960 ◽  
Vol 33 (2) ◽  
pp. 335-341
Author(s):  
Walter Scheele ◽  
Karl-Heinz Hillmer
Keyword(s):  
Activation Energy ◽  
Physical Properties ◽  
Chemical Kinetics ◽  
Kcal Mole ◽  
First Order ◽  
Equilibrium Swelling ◽  
Kinetics Of ◽  
Kinetics Of Vulcanization ◽  
Limiting Value ◽  
Good Agreement

Abstract As a complement to earlier investigations, and in order to examine more closely the connection between the chemical kinetics and the changes with vulcanization time of the physical properties in the case of vulcanization reactions, we used thiuram vulcanizations as an example, and concerned ourselves with the dependence of stress values (moduli) at different degrees of elongation and different vulcanization temperatures. We found: 1. Stress values attain a limiting value, dependent on the degree of elongation, but independent of the vulcanization temperature at constant elongation. 2. The rise in stress values with the vulcanization time is characterized by an initial delay, which, however, is practically nonexistent at higher temperatures. 3. The kinetics of the increase in stress values with vulcanization time are both qualitatively and quantitatively in accord with the dependence of the reciprocal equilibrium swelling on the vulcanization time; both processes, after a retardation, go according to the first order law and at the same rate. 4. From the temperature dependence of the rate constants of reciprocal equilibrium swelling, as well as of the increase in stress, an activation energy of 22 kcal/mole can be calculated, in good agreement with the activation energy of dithiocarbamate formation in thiuram vulcanizations.

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.

STUDIES ON HOMOGENEOUS FIRST ORDER GAS REACTIONS: VII. THE DECOMPOSITION OF ETHYLIDENE DIBUTYRATE AND HEPTYLIDENE DIACETATE

1937 ◽  
Vol 15b (6) ◽  
pp. 247-253 ◽  
Author(s):  
C. C. Coffin ◽  
J. R. Dacey ◽  
N. A. D. Parlee
Keyword(s):  
Activation Energy ◽  
Homologous Series ◽  
Reaction Velocity ◽  
Vapor State ◽  
Specific Reaction ◽  
First Order ◽  
Gas Reactions

Ethylidene dibutyrate and heptylidene diacetate decompose in the vapor state at temperatures between 200° and 300 °C. to form an aldehyde and an anhydride. The reactions are homogeneous, unimolecular, and complete. The activation energy is the same as that previously found for other members of this homologous series. Ethylidene dibutyrate decomposes at the same rate as ethylidene diacetate, and thus provides further evidence that the specific reaction velocity is independent of the size of the anhydride radicals. Heptylidene diacetate decomposes at the same rate as butylidene diacetate. This indicates that after the aldehyde radical has attained a certain size (three or four carbon atoms) the addition of –CH2− groups leaves the specific reaction velocity unchanged. The velocity constants are given by the equations[Formula: see text]

STUDIES ON HOMOGENEOUS FIRST ORDER GAS REACTIONS: II. THE DECOMPOSITION OF THE ISOMERIC ESTERS BUTYLIDENE DIACETATE AND ETHYLIDENE DIPROPIONATE

1932 ◽  
Vol 6 (4) ◽  
pp. 417-427 ◽  
Author(s):  
C. C. Coffin
Keyword(s):  
Activation Energy ◽  
Degrees Of Freedom ◽  
Maximum Energy ◽  
Velocity Measurements ◽  
First Order ◽  
Gas Reactions ◽  
Points Of View ◽  
The Stability ◽  
Future Work ◽  
Internal Degrees Of Freedom

The gaseous decompositions of the esters butylidene diacetate and ethylidene dipropionate have been studied from points of view previously outlined in papers on the decomposition of ethylidene diacetate (2, 3). The decomposition velocities have been measured at initial pressures of from 5 to 56 cm. of mercury and at temperatures between 211 and 265 °C. The reactions are homogeneous and of the first order. They agree with the Arrhenius equation and give 100% yields (within experimental error) of an aldehyde and an anhydride. The preparation of the compounds and improvements in the technique of the velocity measurements are described.While the specific velocities of the three reactions at any temperature are somewhat different, their activation energies are the same. It is suggested that in the case of such simple reactions, which are strictly localized within the molecular structure, the activation energy can be identified as the maximum energy that the reactive bonds may possess and still exist; i.e., it may be taken as a measure of the stability of the bonds which are broken in the reaction. The suggestion is also made that for a series of reactions which have the same activation energy, the specific velocities can be taken as a relative measure of the number of internal degrees of freedom that contribute to the energy of activation. On the basis of these assumptions it becomes possible to use reaction-velocity measurements for the investigation of intramolecular energy exchange. The theoretical significance of the data is further discussed and the scope of future work in this connection is indicated.The monomolecular velocity constants (sec−1) of the decomposition of ethylidene diacetate, ethylidene dipropionate and butylidene diacetate are given respectively by the equations [Formula: see text], [Formula: see text], and [Formula: see text].

Methanation on exfoliated and supported MoS2

1989 ◽  
Vol 67 (5) ◽  
pp. 862-866 ◽  
Author(s):  
Guenter A. Scholz ◽  
S. Roy Morrison
Keyword(s):  
Activation Energy ◽  
Carbon Monoxide ◽  
Transition Metal Catalysts ◽  
Surface Species ◽  
Reaction Products ◽  
Third Order ◽  
Ammonium Heptamolybdate ◽  
First Order ◽  
Methanation Reaction ◽  
Improved Performance

The methanation reaction on MoS2 exfoliated to a thickness of a few layers or less and adsorbed onto alumina is found to be very small. However, by calcining and resulfiding the exfoliated MoS2 catalysts, greatly improved performance is achieved that is at least equal to the commercial catalysts based on ammonium heptamolybdate. The creation of molybdenum oxysulflde surface species therefore appears to be a necessary step toward producing significant methanation rates with exfoliated and supported MoS2. The methanation products are almost exclusively CO2 and CH4, their mole ratios near unity, with otherwise only very much smaller amounts of longer chain hydrocarbons. The activation energy for methanation is generally observed to be near 100 kJ/mol, with the overall reaction being first order in the carbon monoxide concentration and third order in the hydrogen concentration. In contrast to the transition-metal catalysts, no water could be detected in the reaction products of the molybdenum based catalyst. Keywords: methanation reaction on MoS2, exfoliated and supported MoS2 as catalyst.

scholarly journals KINETICS OF PALM OIL TRANSESTERIFICATION IN METHANOL WITH POTASSIUM HYDROXIDE AS A CATALYST

2010 ◽  
Vol 8 (2) ◽  
pp. 219-225
Author(s):  
Yoeswono Yoeswono ◽  
Triyono Triyono ◽  
Iqmal Tahir
Keyword(s):  
Activation Energy ◽  
Palm Oil ◽  
Rate Constants ◽  
Potassium Hydroxide ◽  
Catalyst Concentration ◽  
Time Interval ◽  
Pseudo First Order Reaction ◽  
Exponential Factor ◽  
Potassium Methoxide ◽  
First Order

A study on palm oil transesterification to evaluate the effect of some parameters in the reaction on the reaction kinetics has been carried out. Transesterification was started by preparing potassium methoxide from potassium hydroxide and methanol and then mixed it with the palm oil. An aliquot was taken at certain time interval during transesterification and poured into test tube filled with distilled water to stop the reaction immediately. The oil phase that separated from the glycerol phase by centrifugation was analyzed by 1H-NMR spectrometer to determine the percentage of methyl ester conversion. Temperature and catalyst concentration were varied in order to determine the reaction rate constants, activation energies, pre-exponential factors, and effective collisions. The results showed that palm oil transesterification in methanol with 0.5 and 1 % w/w KOH/palm oil catalyst concentration appeared to follow pseudo-first order reaction. The rate constants increase with temperature. After 13 min of reaction, More methyl esters were formed using KOH 1 % than using 0.5 % w/w KOH/palm oil catalyst concentration. The activation energy (Ea) and pre-exponential factor (A) for reaction using 1 % w/w KOH was lower than those using 0.5 % w/w KOH.   Keywords: palm oil, transesterification, catalyst, first order kinetics, activation energy, pre-exponential factor

scholarly journals Improvement of recovered activity and stability of the Aspergillus oryzae β-galactosidase immobilized on duolite A568 by combination of immobilization methods

2017 ◽  
Vol 23 (4) ◽  
pp. 495-506 ◽  
Author(s):  
Larissa Falleiros ◽  
Bruna Cabral ◽  
Janaína Fischer ◽  
Carla Guidini ◽  
Vicelma Cardoso ◽  
...  
Keyword(s):  
Activation Energy ◽  
Aspergillus Oryzae ◽  
Physical Adsorption ◽  
Cross Linking ◽  
Thermal Deactivation ◽  
Order Model ◽  
First Order ◽  
Immobilized Biocatalyst ◽  
The Stability ◽  
Kinetics Of

The immobilization and stabilization of Aspergillus oryzae ?-galactosidase on Duolite??A568 was achieved using a combination of physical adsorption, incubation step in buffer at pH 9.0 and cross-linking with glutaraldehyde and in this sequence promoted a 44% increase in enzymatic activity as compared with the biocatalyst obtained after a two-step immobilization process (adsorption and cross-linking). The stability of the biocatalyst obtained by three-step immobilization process (adsorption, incubation in buffer at pH 9.0 and cross-linking) was higher than that obtained by two-steps (adsorption and cross-linking) and for free enzyme in relation to pH, storage and reusability. The immobilized biocatalyst was characterized with respect to thermal stability in the range 55-65 ?C. The kinetics of thermal deactivation was well described by the first-order model, which resulted in the immobilized biocatalyst activation energy of thermal deactivation of 71.03 kcal/mol and 5.48 h half-life at 55.0 ?C.

APPLICATION OF CVD DIAMOND FILMS FOR UV THERMOLUMINESCENCE DOSIMETER

2002 ◽  
Vol 16 (06n07) ◽  
pp. 1003-1007 ◽  
Author(s):  
J. AHN ◽  
B. GAN ◽  
Q. ZHANG ◽  
S. F. YOON ◽  
V. LIGATCHEV ◽  
...  
Keyword(s):  
Activation Energy ◽  
Glow Curve ◽  
Diamond Films ◽  
Frequency Factor ◽  
Cvd Diamond ◽  
Order Kinetic ◽  
First Order ◽  
Order Kinetic Model ◽  
Ionizing Radiations ◽  
Trap Activation

This study presents the investigation of CVD diamond for the application of an UV TL dosimeter. A 9-μm-thick film used in this study presents a TL glow curve with a well-defined first-order kinetic peak (at about 273 K), which norm ally presents in the glow curve from ionizing radiations, is not observed. By fitting the glow curve to a first-order kinetic model, the trap activation energy E t = 0.95 eV and frequency factor s = 5.6 x 106 s -1 have been resolved.

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