scholarly journals Analisis Termodinamika dan Kinetika Nanopartikel Karbon (C-Dot) dari Buah Durian Sebagai Inhibitor Korosi Tembaga

KOVALEN ◽  
2021 ◽  
Vol 7 (3) ◽  
pp. 169-177
Author(s):  
Faradisa Anindita ◽  
Noviyan Darmawan ◽  
Zainal Alim Mas'ud
Keyword(s):  
Activation Energy ◽  
Corrosion Rate ◽  
Corrosion Inhibitor ◽  
Reaction Rate ◽  
Electrochemical Reactions ◽  
Physical Interaction ◽  
Copper Corrosion ◽  
Corrosion Prevention ◽  
The Stability ◽  
Spontaneous Reaction

Corrosion is a physical interaction between the metal and its environment, which results in changes in the metal's properties due to chemical or electrochemical reactions. The corrosion rate can be reduced by adding a corrosion inhibitor. Uses of nanotechnology for corrosion prevention is one of the first technical because almost made structures rely on the stability of a 1–2 nm thick passive film which provides stability to the underlying material. Herein we report the thermodynamic and kinetic analysis of carbon-dots from Durian as inhibitor copper corrosion. To test the anticorrosive performance and analyze thermodynamic properties in its role as a corrosion inhibitor on copper using potentiodynamic polarization. The thermodynamic-kinetic parameters of corrosion obtained values of H‡ = 60.44 kJmol-1, ΔS‡ = -73.9 kJmol-1, and ΔG‡ = 82.83 kJmol-1, show that the attendance of C-dot as a corrosion inhibitor causes a non-spontaneous reaction rate to be proven by increasing spontaneity (ΔG‡). The value of activation energy samples was higher than the blank, indicates the presence of C-dot effective to reduce the rate of corrosion of the metal.

Water treatment to reduce internal corrosion in the drinking water distribution system in Oslo

2001 ◽  
Vol 1 (3) ◽  
pp. 91-96 ◽  
Author(s):  
L.J. Hem ◽  
E.A. Vik ◽  
A. Bjørnson-Langen
Keyword(s):  
Water Treatment ◽  
Corrosion Rate ◽  
Distribution System ◽  
Water Distribution ◽  
Treatment Plant ◽  
Water Treatment Plant ◽  
Corrosion Monitoring ◽  
Copper Corrosion ◽  
Iron Corrosion ◽  
Internal Corrosion

In 1995 the new Skullerud water treatment plant was put into operation. The new water treatment includes colour removal and corrosion control with an increase of pH, alkalinity and calcium concentration in addition to the old treatment, which included straining and chlorination only. Comparative measurements of internal corrosion were conducted before and after the installation of the new treatment plant. The effect of the new water treatment on the internal corrosion was approximately a 20% reduction in iron corrosion and a 70% reduction in copper corrosion. The heavy metals content in standing water was reduced by approximately 90%. A separate internal corrosion monitoring programme was conducted, studying the effects of other water qualities on the internal corrosion rate. Corrosion coupons were exposed to the different water qualities for nine months. The results showed that the best protection of iron was achieved with water supersaturated with calcium carbonate. Neither a high content of free carbon dioxide or the use of the corrosion inhibitor sodium silicate significantly reduced the iron corrosion rate compared to the present treated water quality. The copper corrosion rate was mainly related to the pH in the water.

The Application of Corrosion and Scale Inhibitor to Circulating Water

2012 ◽  
Vol 610-613 ◽  
pp. 2591-2594
Author(s):  
Jia Guo Ren ◽  
Qian Qian Wu
Keyword(s):  
Water Treatment ◽  
Power Plant ◽  
Corrosion Rate ◽  
Corrosion Inhibitor ◽  
Economic Efficiency ◽  
Concentration Ratio ◽  
Scale Inhibitor ◽  
Circulating Water

According to the requirements of the circulating water treatment, a corrosion and scale inhibitor which compounded several single corrosion inhibitor and scale inhibitor was prepared, resulting in simplifying the process of operation, improving the concentration ratio of circulating water from 2.2 to 2.8, reducing the sewage volume, and decreasing the corrosion rate and cohesion rate. Therefore, the economic efficiency of the power plant gets greatly improved.

Application of Benzotriazole Corrosion Inhibitor in Synthetic-Based Drilling Fluid and its Overall Impact in Improving Drilling Fluid Functionality

2021 ◽  
Author(s):  
Zhao Xionghu ◽  
Saviour Bassey Egwu ◽  
Deng Jingen ◽  
Miao Liujie
Keyword(s):  
Corrosion Rate ◽  
Corrosion Inhibitor ◽  
Coefficient Of Friction ◽  
Hot Rolling ◽  
Drilling Fluid ◽  
Effect Of Temperature ◽  
Fluid Loss ◽  
Fluid Composition ◽  
Fluid System ◽  
Before And After

Abstract The effect of corrosion inhibitor Benzotriazole on synthetic-based mud system was studied. Rheological performance of the benzotriazole enhanced synthetic-based fluid system was studied and compared against the base mud. To study its effect on dynamic wellbore conditions, different drilling fluid compositions were placed in a hot rolling oven for 16 hours at temperatures 150 °C and 170°C and the effect of temperature on mud properties were studied. Tests carried out include rheological test (before and after hot rolling), filtrate pH, lubricity test, and fluid loss test. The corrosion penetration rate was studied using the weight loss method. Based on experiment results, the synthetic-based mud system which comprised of benzotriazole displayed a reduction in coefficient of friction up to 95.93%. At ambient condition, optimal ratio of mineral oil:benzotriazole (M:B) which gives best lubricity performance on synthetic-based mud system is 80:20. This leads to improved corrosion inhibition and lubricity of the synthetic-based fluid by reducing the coefficient of friction up to 90.13%. Increased temperature led to further decrease in coefficient of friction with a % torque reduction of 95.93 displayed by the 80:20 ratio M:B mud composition at 170 °C. Significant alterations of the mud composition rheological and fluid loss parameters before and after exposure to high temperature in hot rolling oven were not observed. pH values were maintained ≥7 at the dynamic conditions highlighting solubility of the formulated fluid composition and absence of contaminants which can pose significant threats to the rates of corrosion in drill pipes. Increasing the concentration of Benzotriazole led to a reduction in corrosion rate. However, as the temperature effect increased, the corrosion rate elevated. Based on results from this investigation, it was concluded that Benzotriazole can be applied as a corrosion inhibitor in a synthetic-based drilling fluid system as an alternative corrosion inhibitor without significant alteration of the base mud properties. Benefits of this will be the optimization of extended reach well drilling operations due to excellent lubricity performance, corrosion rate reduction, compatibility with HPHT wellbore condition and fluid loss control.

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].

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.

scholarly journals Ibuprofen as a corrosion inhibitor for copper in synthetic acid rain solution

2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Zaklina Z. Tasić ◽  
Marija B. Petrović Mihajlović ◽  
Ana T. Simonović ◽  
Milan B. Radovanović ◽  
Milan M. Antonijević
Keyword(s):  
Acid Rain ◽  
Corrosion Inhibitor ◽  
Quantum Chemical ◽  
Corrosion Inhibitors ◽  
Inhibition Efficiency ◽  
Theoretical Calculations ◽  
Pharmaceutical Compounds ◽  
Copper Corrosion ◽  
A Value ◽  
Synthetic Acid

Abstract It is known that if unused drugs are improperly disposed, they can pollute the environment. Furthermore, researchers are still trying to find an environmentally friendly corrosion inhibitor. These factors lead to the possible application of unused pharmaceutical compounds as corrosion inhibitors. The feasibility of an anti-inflammatory, analgesic and antipyretic drug, ibuprofen, was evaluated as a potential copper corrosion inhibitor in synthetic acid rain solution. This investigation was performed by applying electrochemical and weight loss measurements and quantum chemical calculations. The results obtained by these techniques revealed the ability of ibuprofen to protect copper from corrosion. The inhibition efficiency of ibuprofen rises with increase in its concentration and can reach a value of 97.3%. The results of surface analysis of treated coupons by scanning electron microscopy and theoretical calculations are consistent with the experimental results.

Zur Theorie der Elektronenübergangsreaktionen in molekularen Komplexen / Theory of Electron Transfer Reactions in Molecular Complexes

1974 ◽  
Vol 29 (6) ◽  
pp. 880-887 ◽  
Author(s):  
P. P. Schmidt
Keyword(s):  
Activation Energy ◽  
Electron Transfer ◽  
Charge Transfer ◽  
Rate Constant ◽  
Reaction Rate ◽  
Charge Transfer Complex ◽  
Rate Theory ◽  
Transfer Step ◽  
Donor And Acceptor ◽  
Inner Sphere

This paper reports a theory of the inner sphere-type electron transfer reaction. Inner sphere reactions, as opposed to the outer sphere variety, require that the solvate or ligand shells surrounding the electron donor and acceptor species undergo considerable change in the course of the electron transfer. In this paper we assume that the electron transfer step takes place in a molecular complex which exists in equilibrium with the reactants. The electron transfer step occurs as a non-radiative charge transfer-type transition. In this manner we treat the charge transfer kinetics, in particular, the evaluation of the reaction rate constant, in the same manner as is usual for non-radiative problems. The analysis leading to the rate constant expression is based on Yamamoto’s general chemical reaction rate theory. The rate constant expressions obtained are quite general, they hold for any degree of strength of coupling between subsystems comprising the entire system. The activation energy, in the Arrhenius form for the rate constant, shows a dependence on the energy (work) of formation of the intermediate charge transfer complex, on vibrational shift energies associated with the molecular motions of the ligands, and on solvent repolarization energies. The activation energy also shows an important dependence on coupling terms which link the vibrations of the molecular inner shell with the polarization states of the (assumed) dielectric continuum which surrounds the charge transfer participants. The approach we take in developing this theory we believe points the way towards the development of a more complete theory capable of accounting for the dynamics of the molecular reorganization leading to the intermediate charge transfer complex as well as accounting for the electron transfer step itself.

Kinetic Studies on the Synthesis of Hydroxyapatite Nanowires by Solvothermal Methods

2007 ◽  
Vol 60 (2) ◽  
pp. 99 ◽  
Author(s):  
Shiying Zhang ◽  
Chen Lai ◽  
Kun Wei ◽  
Yingjun Wang
Keyword(s):  
Activation Energy ◽  
Reaction Rate ◽  
Kinetic Studies ◽  
Axial Ratio ◽  
Reaction Rate Constant ◽  
Rate Equations ◽  
Solvothermal Reaction ◽  
Growth Order ◽  
Constant Diffusion ◽  
Solvothermal Methods

Hydroxyapatite nanowires with a high axial ratio have been synthesized in reverse micelle solutions that consist of cetyltrimethylammonium bromide (CTAB), n-pentanol, cyclohexane, and the reactant solution by solvothermal methods. This paper focusses on the kinetic studies of the solvothermal reaction and the linear growth of hydroxyapatite nanowires. When the reaction was carried out at low temperatures (65°C), the experimental results showed that the reaction rate was of zero order since the whole reaction was diffusion controlled with constant diffusion coefficients. In the middle to high temperature range (130–200°C), the kinetics were characterized by second order reaction kinetics. Since the controlling factor was activation energy and the apparent activation energy was large, the reaction rate was more sensitive to the temperature. Therefore, the exponent of the reaction rate constant increased by two when the temperature was increased from 130 to 200°C. By calculating the yields of products and the specific surface areas at different times, the linear and overall growth rate equations of the hydroxyapatite nanowires could be obtained. The experimental effective growth order of the crystals was 11. The larger growth order indicated that the crystal could grow more effectively in one direction because of the induction of the surfactant in the experiment system.

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