scholarly journals KINETIKA FOTODEGRADASI KLOROFIL, TOKOFEROL, DAN KAROTENOID DALAM MINYAK SAWIT MERAH (Photodegradation Kinetics of Chlorophyll, Tocopherol, and Carotenoid in Red Palm Oil)

2016 ◽  
Vol 36 (02) ◽  
pp. 117 ◽  
Author(s):  
Dewi Fortuna Ayu ◽  
Nuri Andarwulan ◽  
Purwiyatno Hariyadi ◽  
Eko Hari Purnomo
Keyword(s):  
Light Intensity ◽  
Rate Constant ◽  
Palm Oil ◽  
Prolonged Storage ◽  
K Value ◽  
Red Palm Oil ◽  
First Order ◽  
First Order Kinetics ◽  
Light Intensities ◽  
Kinetics Of

The objective of this research was to assess the photodegradation kinetics of chlorophyll, tocopherol, and carotenoid in red palm oil (RPO) during storage under flourescent light intensities of 5000, 10000, and 15000 lux. Photodegradation was followed by measuring the changes of chlorophyll, tocopherol, and carotene contents in RPO filled in transparent bottles stored in incubator box (31.60±0.69 oC) with controlled light intensity. As reference, pure RPO was filled in dark and transparent bottles then was stored at roomy temperature (31.46±1.04 °C) and lighting (476.25-484.89lux). The result showed that photodegradation of chlorophyll followed first order kinetics with two distinct photodegradation periods. First, rapid photodegradation period during the first 6 hours of storage with k values of 3.81x10-2, 4.45x10-2, 5.64x10-2 day-1, followed by a slower photodegradation period at prolonged storage more than 6 hours, with k values of 1.41x10-2, 3.01x10-2, 4.59x10-2 day-1 under light intensities of 5000, 10000, and 15000 lux, respectively. Photodegradation of tocopherol and carotene also followed first order kinetics. Photodegradation of tocopherol had the highest rate constant (k value of 9.10x10-2, 12.02x10-2, 17.33x10-2 day-1), meanwhile carotene had the lowest rate constant (k value of 0.80x10-2, 1.40x10-2, 1.98x10-2 day-1) under light intensities of 5000, 10000, and 15000 lux, respectively. The light intensity coefficient (zi) as dependence indicator of k on the changes of light intensity were measured. The zi values ofchlorophyll, tocopherol, and carotene were 20000, 33333, and 25000 lux, respectively; indicated that the degradation rate of chlorophyll was the most sensitive to the changes of light intensity. Keywords: Red palm oil, photo-oxidation, chlorophyll, tocopherol, carotene ABSTRAKPenelitian ini bertujuan untuk mengkaji laju fotodegradasi klorofil, tokoferol, dan karoten dalam minyak sawit merah (MSM) selama penyimpanan dalam kondisi terpapar cahaya fluoresen pada intensitas 5000, 10000, dan 15000 lux. Fotodegradasi dikaji dengan mengukur perubahan kadar klorofil, tokoferol, dan karoten MSM pada botol transparan yang disimpan dalam kotak inkubator (31,60±0,69 oC) dengan intensitas cahaya dipertahankan konstan. Sebagai pembanding, MSM murni dalam botol gelap dan transparan disimpan pada suhu (31,46±1,04 °C) dan pencahayaan normal laboratorium (476,25-484,89 lux). Hasil penelitian menunjukkan bahwa klorofil mengalami fotodegradasi mengikuti model reaksi ordo pertama dalam dua periode; yaitu periode fotodegradasi cepat selama penyimpanan 6 jam pertama dengan nilai konstanta laju (k) 3,81x10-2, 4,45x10-2, 5,64x10-2 hari-1, diikuti periode fotodegradasi lambat pada penyimpanan yang lebih lama dengan nilai k 1,41x10-2, 3,01x10-2, 4,59x10-2 hari-1 masing-masing pada intensitas cahaya 5000, 10000, dan 15000 lux. Fotodegradasi tokoferol dan karoten juga mengikuti model reaksi ordo pertama. Fotodegradasi tokoferol berlangsung dengan laju paling tinggi (nilai k 9,10x10-2, 12,02x10-2, 17,33x10-2 hari-1), sedangkan fotodegradasi karoten berlangsung dengan laju paling rendah (nilai k 0,80x10-2, 1,40x10-2, 1, 98x10-2 hari-1) masing-masing pada perlakuan intensitas cahaya 5000, 10000, dan 15000 lux. Konstanta intensitas cahaya (zi) sebagai indikator ketergantungan nilai k terhadap perubahan intensitas cahaya untuk klorofil, tokoferol, karoten berturut-turut adalah 20000, 33333, dan 25000 lux. Hal ini mengindikasikan bahwa laju degradasi klorofil paling sensitif terhadap perubahan intensitas cahaya. Kata kunci: Minyak sawit merah, foto-oksidasi, klorofil, tokoferol, karoten

Kinetics of the Ce3+/BrO2-Reaction in Sulfuric Acid Medium

1985 ◽  
Vol 40 (4) ◽  
pp. 368-372 ◽  
Author(s):  
H. D. Försterling ◽  
H. J. Lamberz ◽  
H. Schreiber
Keyword(s):  
Sulfuric Acid ◽  
Acid Solution ◽  
Acid Medium ◽  
Rate Constant ◽  
Constant Concentration ◽  
First Order ◽  
Sulfuric Acid Medium ◽  
First Order Kinetics ◽  
Belousov Zhabotinsky Reaction ◽  
Kinetics Of

The reaction of Ce3+ with BrO2 in sulfuric acid solution (which is the starting step in the inorganic reaction subset of the Belousov-Zhabotinsky-reaction) is followed spectroscopically in a reaction mixture containing BrO2 at constant concentration. From first order kinetics (Br02 in excess) the rate constant for this reaction is evaluated.

scholarly journals Belousov-Zhabotínsky oscillatory reaction. Kinetics of malonic acid decomposition

2000 ◽  
Vol 65 (10) ◽  
pp. 709-713 ◽  
Author(s):  
Slavica Blagojevic ◽  
Natasa Pejic ◽  
Slobodan Anic ◽  
Ljiljana Kolar-Anic
Keyword(s):  
Sulfuric Acid ◽  
Reaction Kinetics ◽  
Rate Constant ◽  
Malonic Acid ◽  
Oscillatory Reaction ◽  
Acid Decomposition ◽  
First Order ◽  
First Order Kinetics ◽  
Pseudo First Order ◽  
Kinetics Of

The kinetics of the Belousov-Zhabotinsky (BZ) oscillatory reaction was analyzed. With this aim, the tune evolution of a reactionmixture composedof malonic acid, bromate, sulfuric acid and cerium(III) was studied at 298 K. Pseudo-first order kinetics with respect to malonic acid as the species undergoing decomposition with a corresponding rate constant, k = 7.5x10-3 min-1, was found.

Kinetic of oxidation of methyl orange by vanadium(V) under conditions VO2+ and decavanadates coexist: Catalysis by Triton X-100 micellar medium

2019 ◽  
Author(s):  
Chem Int
Keyword(s):  
Methyl Orange ◽  
Solution Ph ◽  
Vanadium Concentration ◽  
Limiting Behavior ◽  
First Order ◽  
First Order Kinetics ◽  
Ph Range ◽  
Kinetic Pattern ◽  
Triton X ◽  
Kinetics Of

The kinetics of oxidation of methyl orange by vanadium(V) {V(V)} has been investigated in the pH range 2.3-3.79. In this pH range V(V) exists both in the form of decavanadates and VO2+. The kinetic results are distinctly different from the results obtained for the same reaction in highly acidic solution (pH < 1) where V(V) exists only in the form of VO2+. The reaction obeys first order kinetics with respect to methyl orange but the rate has very little dependence on total vanadium concentration. The reaction is accelerated by H+ ion but the dependence of rate on [H+] is less than that corresponding to first order dependence. The equilibrium between decavanadates and VO2+ explains the different kinetic pattern observed in this pH range. The reaction is markedly accelerated by Triton X-100 micelles. The rate-[surfactant] profile shows a limiting behavior indicative of a unimolecular pathway in the micellar pseudophase.

scholarly journals Comparative Study of Chemical Stability of Two H1Antihistaminic Drugs, Terfenadine and ItsIn VivoMetabolite Fexofenadine, Using LC-UV Methods

2019 ◽  
Vol 2019 ◽  
pp. 1-10
Author(s):  
Anna Gumieniczek ◽  
Anna Berecka-Rycerz ◽  
Rafał Pietraś ◽  
Izabela Kozak ◽  
Karolina Lejwoda ◽  
...  
Keyword(s):  
Comparative Study ◽  
Chemical Stability ◽  
First Order ◽  
First Order Kinetics ◽  
Kinetics Of Degradation ◽  
Effects Of Temperature ◽  
High Doses ◽  
Antihistaminic Drugs ◽  
Kinetics Of

A comparative study of chemical stability of terfenadine (TER) and itsin vivometabolite fexofenadine (FEX) was performed. Both TER and FEX were subjected to high temperature at different pH and UV/VIS light at different pH and then quantitatively analyzed using new validated LC-UV methods. These methods were used to monitor the degradation processes and to determine the kinetics of degradation for both the compounds. As far as the effects of temperature and pH were concerned, FEX occurred more sensitive to degradation than TER. As far as the effects of UV/VIS light and pH were concerned, the both drugs were similarly sensitive to high doses of light. Using all stress conditions, the processes of degradation of TER and FEX followed the first-order kinetics. The results obtained for these two antihistaminic drugs could be helpful in developing their new derivatives with higher activity and stability at the same time.

Preparation, Solubility, Infrared Spectra and Radiolysis of Tetramethylammonium Hydrogenselenate Monohydrate and Lithium Tetramethylammonium Selenate Tetrahydrate

2006 ◽  
Vol 71 (3) ◽  
pp. 411-422 ◽  
Author(s):  
David Havlíček ◽  
Libor Turek ◽  
Jiří Plocek ◽  
Zdeněk Mička
Keyword(s):  
Chemical Analysis ◽  
Rate Constant ◽  
Infrared Spectra ◽  
Molecular Spectroscopy ◽  
Anhydrous Salt ◽  
First Order ◽  
First Order Kinetics ◽  
New Compounds

Solubility in the (Me4N)2SeO4-H2SeO4-H2O and (Me4N)2SeO4-Li2SeO4-H2O systems were studied. The new compounds, tetramethylammonium hydrogenselenate monohydrate ((Me4N)HSeO4·H2O) and lithium tetramethylammonium selenate tetrahydrate (Li(Me4N)SeO4·4H2O), have been found in these systems. Both substances were characterised by chemical analysis and IR molecular spectroscopy. Both of the title substances decompose under the influence of X-radiation and, thus, their structures cannot be determined. The radiolysis of both substances was studied in greater detail. Tetramethylammonium hydrogenselenate monohydrate is dehydrated by X-radiation to form the anhydrous salt. The reaction is controlled by first-order kinetics with a rate constant of 1.30(3) × 10-3 s-1.

Spectrochemical Behavior of Carcinogenic Polycyclic Aromatic Hydrocarbons in Biological Systems. Part II: A Theoretical Rate Model for BaP Metabolism in Living Cells

1996 ◽  
Vol 50 (11) ◽  
pp. 1352-1359 ◽  
Author(s):  
Ping Chiang ◽  
Kuang-Pang Li ◽  
Tong-Ming Hseu
Keyword(s):  
Rate Constant ◽  
Living Cells ◽  
Rate Model ◽  
Number Density ◽  
Order Process ◽  
Irreversible Reaction ◽  
First Order ◽  
Metabolism Rate ◽  
Polycyclic Aromatic ◽  
Kinetics Of

An idealized model for the kinetics of benzo[ a]pyrene (BaP) metabolism is established. As observed from experimental results, the BaP transfer from microcrystals to the cell membrane is definitely a first-order process. The rate constant of this process is signified as k1. We describe the surface–midplane exchange as reversible and use rate constants k2 and k3 to describe the inward and outward diffusions, respectively. The metabolism is identified as an irreversible reaction with a rate constant k4. If k2 and k3 are assumed to be fast and not rate determining, the effect of the metabolism rate, k4, on the number density of BaP in the midplane of the microsomal membrane, m3, can be estimated. If the metabolism rate is faster than or comparable to the distribution rates, k2 and k3, the BaP concentration in the membrane midplane, m3, will quickly be dissipated. But if k4 is extremely small, m3 will reach a plateau. Under conditions when k2 and k3 also play significant roles in determining the overall rate, more complicated patterns of m3 are expected.

scholarly journals Kinetics of thiamin cleavage by sulphite

1969 ◽  
Vol 113 (4) ◽  
pp. 611-615 ◽  
Author(s):  
J. Leichter ◽  
M. A. Joslyn
Keyword(s):  
Aqueous Solutions ◽  
Rate Constant ◽  
Sulphur Dioxide ◽  
First Order ◽  
Ph Values ◽  
Rate Of Reaction ◽  
Kinetics Of

Results are presented on the rate of thiamin cleavage by sulphite in aqueous solutions as affected by temperature (20–70°), pH(2·5–7·0), and variation of the concentration of either thiamin (1–20μm) or sulphite (10–5000μm as sulphur dioxide). Plots of the logarithm of percentage of residual thiamin against time were found to be linear and cleavage thus was first-order with respect to thiamin. At pH5 the rate was also found to be proportional to the sulphite concentration. In the pH region 2·5–7·0 at 25° the rate constant was 50m−1hr.−1 at pH5·5–6·0, and decreased at higher or lower pH values. The rate of reaction increased between 20° and 70°, indicating a heat of activation of 13·6kcal./mole.

Oxidation of Nickel(II) and Manganese(II) by Peroxodisulfate in Aqueous Solution in the Presence of Molybdate. Crystal Structure of the (NH4)6[NiMo9O32].6H2O Product

1992 ◽  
Vol 45 (12) ◽  
pp. 1943 ◽  
Author(s):  
SJ Dunne ◽  
RC Burns ◽  
GA Lawrance
Keyword(s):  
Rate Constant ◽  
Linear Dependence ◽  
Ph Dependence ◽  
Order Rate Constant ◽  
X Ray Diffraction ◽  
X Ray ◽  
First Order ◽  
Oxidant Concentration ◽  
Ph Range ◽  
Kinetics Of

Oxidation of Ni2+,aq, by S2O82- to nickel(IV) in the presence of molybdate ion, as in the analogous manganese system, involves the formation of the soluble heteropolymolybdate anion [MMogO32]2- (M = Ni, Mn ). The nickel(IV) product crystallized as (NH4)6 [NiMogO32].6H2O from the reaction mixture in the rhombohedra1 space group R3, a 15.922(1), c 12.406(1) � ; the structure was determined by X-ray diffraction methods, and refined to a residual of 0.025 for 1741 independent 'observed' reflections. The kinetics of the oxidation were examined at 80 C over the pH range 3.0-5.2; a linear dependence on [S2O82-] and a non-linear dependence on l/[H+] were observed. The influence of variation of the Ni/Mo ratio between 1:10 and 1:25 on the observed rate constant was very small at pH 4.5, a result supporting the view that the precursor exists as the known [NiMo6O24H6]4- or a close analogue in solution. The pH dependence of the observed rate constant at a fixed oxidant concentration (0.025 mol dm-3) fits dequately to the expression kobs = kH [H+]/(Ka+[H+]) where kH = 0.0013 dm3 mol-1 s-1 and Ka = 4-0x10-5. The first-order dependence on peroxodisulfate subsequently yields a second-order rate constant of 0.042 dm3 mol-1 s-1. Under analogous conditions, oxidation of manganese(II) occurs eightfold more slowly than oxidation of nickel(II), whereas oxidation of manganese(II) by peroxomonosulfuric acid is 16-fold faster than oxidation by peroxodisulfate under similar conditions.

scholarly journals EFFECT OF DIATOMEAOUS EARTH TREATMENT USING HYDROGEN CHLORIDE AND SULFURIC ACID ON KINETICS OF CADMIUM(II) ADSORPTION

2010 ◽  
Vol 2 (2) ◽  
pp. 107-112
Author(s):  
Nuryono Nuryono ◽  
Narsito Narsito
Keyword(s):  
Aqueous Solution ◽  
Sulfuric Acid ◽  
Hydrogen Chloride ◽  
Rate Constant ◽  
Diatomaceous Earth ◽  
Adsorption Rate ◽  
Physical Interaction ◽  
First Order ◽  
Adsorption Rate Constant ◽  
Kinetics Of

In this research, treatment of diatomaceous earth, Sangiran, Central Java using hydrogen chloride (HCl) and sulfuric acid (H2SO4) on kinetics of Cd(II) adsorption in aqueous solution has been carried out. The work was conducted by mixing an amount of grounded diatomaceous earth (200 mesh in size) with HCl or H2SO4 solution in various concentrations for two hours at temperature range of 100 - 150oC. The mixture was then filtered and washed with water until the filtrate pH is approximately 7 and then the residue was dried for four hours at a temperature of 70oC. The product was used as an adsorbent to adsorb Cd(II) in aqueous solution with various concentrations. The Cd(II) adsorbed was determined by analyzing the rest of Cd(II) in the solution using atomic absorption spectrophotometry. The effect of treatment was evaluated from kinetic parameter of adsorption rate constant calculated based on the simple kinetic model. Results showed  that before equilibrium condition reached, adsorpstion of Cd(II) occurred through two steps, i.e. a step tends to follow a reaction of irreversible first order  (step I) followed by reaction of reversible first order (step II). Treatment with acids, either hydrogen chloride or sulfuric acid, decreased adsorption rate constant for the step I from 15.2/min to a range of 6.4 - 9.4/min.  However, increasing concentration of acid (in a range of concentration investigated) did not give significant and constant change of adsorption rate constant. For step II process,  adsorption involved physical interaction with the sufficient low adsorption energy (in a range of 311.3 - 1001 J/mol).     Keywords: adsorption, cdmium, diatomaceous earth, kinetics.

Modified ferron assay for speciation characterization of hydrolyzed Al(III): a precise k value based judgment

2009 ◽  
Vol 59 (4) ◽  
pp. 823-832 ◽  
Author(s):  
Ye Changqing ◽  
Wang Dongsheng ◽  
Wu Xiaohong ◽  
Qu Jiuhui ◽  
John Gregory
Keyword(s):  
Kinetic Constant ◽  
Nonlinear Least Squares ◽  
Precise Determination ◽  
K Value ◽  
First Order ◽  
First Order Kinetics ◽  
Parallel Reactions

The speciation of Al-OH complexes in terms of Ala, Alb and Alc could be achieved by traditional ferron assay and Alb is generally considered as Al13, however, the inherent correlation between them remains an enigma. This paper presents a modified ferron assay to get precise determination of Al13 using nonlinear least squares analysis, and to clarify the correlation between Alb and Al13. Two parallel reactions conforming to pseudo-first-order kinetics can simulate the complicate reactions between polynuclear complexes and ferron successfully. Four types of experimental kinetic constant (k value) of Al-OH complexes can be observed by this method when investigating three typical aluminium solutions. Comparing with the results of 27Al NMR, the species with moderate kinetics around 0.001 s−1 can be confirmed to resemble to Al13 polycation. The other types of kinetics are also well-regulated in partially neutralized aluminium solutions with various OH/Al ratios (b values) in the range 0 ∼ 2.5. It would provide potential means to trace the in-situ formation of Al13 in dilute solutions such as coagulation with Al-based coagulants

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