<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">OJOGas</journal-id><journal-title-group><journal-title>Open Journal of Yangtze Oil and Gas</journal-title></journal-title-group><issn pub-type="epub">2473-1889</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/ojogas.2023.81001</article-id><article-id pub-id-type="publisher-id">OJOGas-122363</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Engineering</subject></subj-group></article-categories><title-group><article-title>
 
 
  Modeling and Study Influence of the Temperature Parameter on Corrosion Factors in the Atmospheric Distillation Column of Crude Oil
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Ndiassé</surname><given-names>Fall</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Dialo</surname><given-names>Diop</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Sossé</surname><given-names>Ndiaye</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Kharouna</surname><given-names>Talla</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Haroun</surname><given-names>Ali Adannou</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Astou</surname><given-names>Sarr</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Aboubaker</surname><given-names>Chèdikh Beye</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>Groupe de Laboratoire de Physique des Solides et Sciences des Matériaux, Faculté des Sciences et Techniques, Université Cheikh Anta Diop de Dakar, Dakar, Sénégal</addr-line></aff><aff id="aff2"><addr-line>Département Génie Chimique, Institut National Supérieur de Pétrole de Mao, Mao, Tchad</addr-line></aff><pub-date pub-type="epub"><day>11</day><month>01</month><year>2023</year></pub-date><volume>08</volume><issue>01</issue><fpage>1</fpage><lpage>10</lpage><history><date date-type="received"><day>12,</day>	<month>December</month>	<year>2022</year></date><date date-type="rev-recd"><day>9,</day>	<month>January</month>	<year>2023</year>	</date><date date-type="accepted"><day>12,</day>	<month>January</month>	<year>2023</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  Atmospheric distillation is the first step in separating crude oil into by-products. It uses the different boiling temperatures of the components of crude oil to separate them. But crude oil contains a large quantity of acids and corrosive gases, including sulfur compounds, naphthenic acids, carbon dioxide, oxygen, etc. However, the temperature has an important influence on the aggressiveness of the corrosion factors in the atmospheric distillation column. This paper aims to investigate the role of temperature on corrosive products in the atmospheric distillation column. The results of the developed model show that the temperature increases the corrosion rate in the atmospheric distillation column but above a certain temperature value (about 600 K), it decreases. This illustrates the dual role played by temperature in the study of corrosion within the atmospheric distillation column.
 
</p></abstract><kwd-group><kwd>Atmospheric Distillation</kwd><kwd> Corrosion</kwd><kwd> Crude Oil</kwd><kwd> Materials</kwd><kwd> Temperature</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Our research covers three areas, namely: petrochemistry, materials science and thermodynamics, which are inseparable in the petroleum industry. Prospecting, depositing, refining and transporting products derived from crude oil require in-depth knowledge of the links between these three areas. Since the first researches and results on corrosion in mining, refining especially in the distillation and processing of crude oil, temperature has always been a determining factor. However, its behavior is complex; some believe that corrosion increases directly with temperature, others tend to minimize its effects on corrosion. At the beginning of researches on the link between temperature and corrosion, many specialists showed that corrosion increases with temperature. An old rule of thumb is that increasing the temperature to 283 K doubles the corrosion rate [<xref ref-type="bibr" rid="scirp.122363-ref1">1</xref>]. This approximation gives an idea of ​​the influence that temperature can have on corrosion, although this rule can be misleading in certain situations. On the other hand, over time, some specialists have demonstrated the inhibition of the proliferation of corrosion beyond a certain temperature value for the corrosion of naphthenic acid, the corrosion by carbon dioxide and the corrosion of sulfur compounds [<xref ref-type="bibr" rid="scirp.122363-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.122363-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.122363-ref4">4</xref>].</p><p>Firstly, it is necessary to differentiate between the temperature of the wall and the temperature of the medium. It is the latter that is considered in this article and that we will use in the rest of our discussion. In furnaces and in the event of a significant difference between these two values, the one that prevails is the temperature of the walls if the temperature in the medium does not modify its composition [<xref ref-type="bibr" rid="scirp.122363-ref2">2</xref>].</p><p>At room temperature, naphthalene acids are not corrosive. However, it becomes more aggressive at temperatures where refining takes place [<xref ref-type="bibr" rid="scirp.122363-ref5">5</xref>]. Naphthalene acid becomes corrosive to carbon steel at temperature ranging from 473 to 493 K, respectively and reaches its peak activity at 583 K. The corrosivity of Naphthalene is minimal above 673 K due to its decomposition at high temperatures [<xref ref-type="bibr" rid="scirp.122363-ref5">5</xref>].</p><p>Temperature strongly affects the nature and morphology of corrosion deposits that form on the surface of low alloy steels. For temperatures above 343 K, the low solubility of FeCO<sub>3</sub> and the high saturation in the latter promote the formation of a protective iron carbonate deposit [<xref ref-type="bibr" rid="scirp.122363-ref3">3</xref>]. Below 343 K, the temperature activates the process of electronic dissolution of steel [<xref ref-type="bibr" rid="scirp.122363-ref6">6</xref>].</p><p>Sulfur corrosion intensifies with increasing temperature from 503 K and is maximal at temperatures (698 - 723 K) [<xref ref-type="bibr" rid="scirp.122363-ref7">7</xref>]. Beyond these temperatures, the corrosion of sulfur compounds decreases with increasing temperature up to 813 K. At temperatures above 698 K, the greatest amount of corrosive sulfur has reacted with the metal surface or decomposed and there is a formation of a dense coke deposit, which prevents corrosion from proliferating [<xref ref-type="bibr" rid="scirp.122363-ref4">4</xref>].</p><p>Temperature and pressure affect the nature of the phases (liquid, solid and gaseous) which in turn can cause significant corrosion damage [<xref ref-type="bibr" rid="scirp.122363-ref8">8</xref>]. The increase in temperature accelerates the electrochemical reactions of corrosion and the transfer of aggressive substances on the surface of metals. A rise in temperature causes a drop in the pH of the water. This results in a proliferation of corrosion. In another sense, the solubility of aggressive gases (H<sub>2</sub>S, O<sub>2</sub>, CO<sub>2</sub>) decreases with increasing temperature. Therefore, temperature has a complicated effect on corrosion. Above a certain temperature, corrosion increases considerably and then decreases due to the reduction in the solubility of corrosion-causing gases in aqueous solutions. Generally, it is between 333 - 353 K depending on the chemical composition of the liquid phase [<xref ref-type="bibr" rid="scirp.122363-ref9">9</xref>]. In addition, temperature increases the rate of sedimentation and the formation of a protective FeCO<sub>3</sub> layer [<xref ref-type="bibr" rid="scirp.122363-ref4">4</xref>].</p><p>It is therefore necessary to provide a scientific answer to this problem.</p><p>This paper aims to carry out a study on this problem in order to give the behavior of the corrosion factors with regard to temperature and to define by a mathematical modeling of the evolution of the mass loss according to the temperature within the atmospheric distillation column.</p><p>The rest of this article is subdivided into three parts. The first part is the materials and methods used, then the presentation and discussion of the results, and in the last part we have resumed this work and given the perspectives for developing, and eventually apply these results in industry.</p></sec><sec id="s2"><title>2. Materials and Methods</title><sec id="s2_1"><title>2.1. Materials</title><p>To illustrate the effect of temperature on corrosion factors through programming softwares, the time (X) and temperature (Y) parameters are varied in order to observe the behavior of the representative curves of the mass loss (P<sub>1</sub>(X,Y) for the linear Equation (6) and P<sub>2</sub>(X,Y) for the second order polynomial Equation (7)).</p><p>Firstly we study the behavior of these two equations for times Y from 0 to 10 h and temperatures X from 600 to 1000 K in accordance with the operating temperatures of the atmospheric distillation column.</p><p>Secondly, the time parameter Y is varied from 0 to 1000 h and temperature stays from 600 tom 1000 K.</p></sec><sec id="s2_2"><title>2.2. Methods</title><p>The rate of corrosion can be related to temperature, based on the Arrhenius equation [<xref ref-type="bibr" rid="scirp.122363-ref10">10</xref>]:</p><p>R = A exp ( − E a R T ) (1)</p><p>R is the speed constant of corrosion reaction; A is the Arrhenius constant; R is the noble gases constant (J/K&#183;mol); T is temperature (K) and Ea is the activation energy of the reaction (KJ/mol).</p><p>Furthermore, the experimental results show that the corrosion rate increased with time to the power n, R is proportional to [<xref ref-type="bibr" rid="scirp.122363-ref10">10</xref>]:</p><p>t n exp ( − 1 T ) (2)</p><p>Therefore, a new exponential model is proposed to correlate corrosion rate data as a function of temperature T and time t [<xref ref-type="bibr" rid="scirp.122363-ref10">10</xref>]:</p><p>R = a 7 C a 8 exp ( − a 9 T ) (3)</p><p>a<sub>7</sub>, a<sub>8</sub>, a<sub>9</sub> and C are constants.</p><p>Mathematical and statistical analyzes provide a powerful approach for the dependence of corrosion rate on temperature and time [<xref ref-type="bibr" rid="scirp.122363-ref11">11</xref>]. Statistical and mathematical relationships can be used to prevent the evolution of corrosion in the atmospheric distillation column under conditions different from the experimental conditions.</p><p>Mathematical regression can be used, as it is the predominant method for illustrating computer data [<xref ref-type="bibr" rid="scirp.122363-ref12">12</xref>].</p><p>Several mathematical equations can be suggested for the mathematical illustration of the mass loss of low carbon steels as a function of temperature and time [<xref ref-type="bibr" rid="scirp.122363-ref13">13</xref>] [<xref ref-type="bibr" rid="scirp.122363-ref14">14</xref>]. The linear Equation (4) and the second-order polynomial Equation (5) are examples [<xref ref-type="bibr" rid="scirp.122363-ref12">12</xref>]:</p><p>P a 1 ( T , t ) = a 0 + a 1 T + a 2 t (4)</p><p>P a 2 ( T , t ) = a 0 + a 1 T + a 2 t + a 3 T t + a 4 T 2 + a 5 t 2 (5)</p><p>P a 1 and P a 2 represent the mass loss in (g/m<sup>2</sup>) and t is the time in (hour h) and from a<sub>0</sub> to a<sub>5</sub> which are constants.</p><p>Equations (3) and (4) can be developed and the regression method is used for this purpose to evaluate the coefficients up to these equations. STATISTICA 7 software is used to estimate these coefficients. This software is based on the nonlinear estimates of the Levenberg-Marquardt least squares method. The maximum number of iterations is 1000, the confidence level is 95% and the critical convergence is 10<sup>6</sup>.</p><p>These equations can be rewritten as follows [<xref ref-type="bibr" rid="scirp.122363-ref12">12</xref>]:</p><p>P 1 ( T , t ) = − 0.162 + 6.5 &#215; 10 − 4 T + 3 &#215; 10 − 3 t (6)</p><p>P 2 ( T , t ) = 0.545 − 1.9 &#215; 10 − 2 T + 2.26 &#215; 10 − 3 t + 2.04 &#215; 10 − 6 T t       + 2.3 &#215; 10 − 6 T 2 − 7.5 &#215; 10 − 6 t 2 (7)</p><p>The numerical values ​​of the coefficients (a<sub>0</sub>-a<sub>5</sub>) are given in Equations (6) and (7).</p><p>Equation (6) represents the mass loss with a computational correlation of R<sup>2</sup> = 0.9834. However, Equation (7) is slightly more rigorous with a correlation of 0.9904 [<xref ref-type="bibr" rid="scirp.122363-ref12">12</xref>]. In general, the correlation coefficient greater than 0.3 signifies a weak relationship between parameters and uncertain validity. Between 0.5 and 0.7, it indicates a significant relationship between the parameters and practical importance. On the other hand, a correlation of 0.9 signifies a significant relationship between the parameters [<xref ref-type="bibr" rid="scirp.122363-ref13">13</xref>] [<xref ref-type="bibr" rid="scirp.122363-ref14">14</xref>].</p><p>Equations (6) and (7) represent the mass loss in the atmospheric distillation column with an acceptable validity criterion, and a good dependence of the parameters: time, temperature and mass loss.</p><p>To show the influence of temperature on the proliferation of corrosion we use the linear Equation (6):</p><p>&#183; For time between 0 - 10 hours and temperature 600 - 1000 K (<xref ref-type="fig" rid="fig1">Figure 1</xref>(a)).</p><p>&#183; For a time between 0 to 1000 hours (6 months) and a temperature of 600 to 1000 K (<xref ref-type="fig" rid="fig1">Figure 1</xref>(b)).</p><p>To show the influence of temperature on corrosion inhibition we use the second order polynomial Equation (7):</p><p>&#183; For time between 0 - 10 h and temperature 600 - 1000 K (<xref ref-type="fig" rid="fig2">Figure 2</xref>(a)).</p><p>&#183; For a time between 0 to 1000 h and a temperature between 600 to 1000 K (<xref ref-type="fig" rid="fig2">Figure 2</xref>(b)).</p><p>The mass loss is given by the expression [<xref ref-type="bibr" rid="scirp.122363-ref15">15</xref>]:</p><p>P = M i − M f S (8)</p><p>where P is the mass loss in (g/cm<sup>2</sup>) M<sub>i</sub> is the initial mass and M<sub>f</sub> the final mass of the metal sample studied in (g) and S is the surface in (m<sup>2</sup>).</p></sec></sec><sec id="s3"><title>3. Results and Discussions</title><sec id="s3_1"><title>3.1. Results</title><sec id="s3_1_1"><title>3.1.1. The Linear Equation (6)</title><p>The linear Equation (6) in <xref ref-type="fig" rid="fig1">Figure 1</xref> shows at <xref ref-type="fig" rid="fig1">Figure 1</xref>(a) and <xref ref-type="fig" rid="fig1">Figure 1</xref>(b) that despite these changes in the parameters, the mass loss increases considerably with temperature and time in the atmospheric distillation column. This constitutes the primary role of temperature on corrosion. These results relate the behavior of corrosion factors with temperature. Corrosion is accelerated if the temperature of the medium grows until a certain value.</p></sec><sec id="s3_1_2"><title>3.1.2. The Second Order Polynomial Equation (7)</title><p>The second order polynomial Equation (7) in <xref ref-type="fig" rid="fig2">Figure 2</xref> shows at <xref ref-type="fig" rid="fig2">Figure 2</xref>(a) and <xref ref-type="fig" rid="fig2">Figure 2</xref>(b) for different mass loss scales that the mass loss decreases with time and temperature.</p><p>The difference in mass loss scales is explained by the important difference in mass loss if time is varied from 10 to 1000 h. This influence of temperature in the corrosion factors in the atmospheric distillation column constitutes the secondary role of temperature on corrosion. These results show that above 673 K the corrosion is inhibited in the atmospheric distillation column.</p></sec></sec><sec id="s3_2"><title>3.2. Discussion</title><sec id="s3_2_1"><title>3.2.1. Influence of Temperature on the Proliferation of Corrosion</title><p>In fact, corrosion is caused in the atmospheric distillation column by certain substances present in the crude oil such as naphthenic acids, carbon dioxide and mainly by sulfur compounds. The corrosivity of these substances increases with temperature as shown in <xref ref-type="fig" rid="fig1">Figure 1</xref> and confirmed by the investigations of some authors in corrosion factors through the atmospheric distillation column. However, the corrosion of naphthenic acids causes significant damage to refinery installations when the temperature is between 493 - 673 K and temperatures lower than these favor low corrosion rates [<xref ref-type="bibr" rid="scirp.122363-ref2">2</xref>].</p><p>The corrosion caused by carbon dioxide increases until it reaches a peak at about 343 K [<xref ref-type="bibr" rid="scirp.122363-ref3">3</xref>]. As for sulfur corrosion, it intensifies with increasing temperature from 503 K and reaches a peak at temperatures (698 - 723 K) [<xref ref-type="bibr" rid="scirp.122363-ref4">4</xref>]. The temperature affects the nature of the phases (solid, liquid, gas) which can cause significant corrosion damage. Indeed, a rise in temperature accelerates the electrochemical reactions of corrosion and the transfer of aggressive substances on the surface of metals. This increase also causes a drop in the pH of the water, hence the increase in corrosion [<xref ref-type="bibr" rid="scirp.122363-ref8">8</xref>].</p></sec><sec id="s3_2_2"><title>3.2.2. Influence of Temperature on Corrosion Inhibition</title><p>The corrosivity of the corrosion factors decreases with temperature above (600 K) as shown in <xref ref-type="fig" rid="fig2">Figure 2</xref> and investigated by some authors in the corrosion factors through the atmospheric distillation column. The corrosivity of Naphthalene is minimal above 673 K due to its decomposition at high temperatures [<xref ref-type="bibr" rid="scirp.122363-ref5">5</xref>].</p><p>Laboratory tests have shown that corrosion increases with an increase in temperature before decreasing considerably beyond a certain temperature value. Iron carbonate FeCO<sub>3</sub> acts as a protective layer in the case of corrosion by carbon dioxide, which reduces corrosion at high temperature [<xref ref-type="bibr" rid="scirp.122363-ref3">3</xref>]. Temperature strongly affects the nature and morphology of corrosion deposits that form on the surface of low alloy steels. Temperatures above 343 K cause the low solubility of the iron carbonate FeCO<sub>3</sub>, hence the saturation of the medium with this substance, which constitutes a protective layer on the iron [<xref ref-type="bibr" rid="scirp.122363-ref3">3</xref>]. Beyond (698 - 723 K) the corrosion of sulfur compounds decreases with increasing temperature up to 813 K [<xref ref-type="bibr" rid="scirp.122363-ref4">4</xref>]. For temperatures above 698 K, most of the corrosive sulfur has already reacted with the surface or decomposed and there is formation of a dense coke deposit, which prevents the proliferation of corrosion [<xref ref-type="bibr" rid="scirp.122363-ref4">4</xref>].</p><p>The solubility of aggressive gases (H<sub>2</sub>S, O<sub>2</sub>, CO<sub>2</sub>) decreases with increasing temperature. Therefore, temperature has a complicated effect on corrosion. Above a certain temperature, corrosion increases considerably and then decreases due to the reduction in the solubility of corrosion-causing gases in aqueous solutions. Generally, it is between 333 - 353 K depending on the chemical composition of the liquid phase [<xref ref-type="bibr" rid="scirp.122363-ref9">9</xref>]. In addition, temperature increases the rate of sedimentation and the formation of a protective FeCO<sub>3</sub> layer [<xref ref-type="bibr" rid="scirp.122363-ref4">4</xref>].</p><p>Negative mass losses are due to deposits such as iron carbonate FeCO<sub>3</sub> and cokes, which form on the surface of metals thus increasing their mass [<xref ref-type="bibr" rid="scirp.122363-ref15">15</xref>].</p><p>To remedy this, scientists soak the steel in air after testing, then they put it in a chemical solution thermostated with ultrasound which eliminates the corrosion products formed on the surface by the molten salts and reveals the healthy metal [<xref ref-type="bibr" rid="scirp.122363-ref15">15</xref>].</p><p>This study of the influence of the temperature parameter on the corrosion factors in the atmospheric distillation column enabled us to establish <xref ref-type="table" rid="table1">Table 1</xref>. This table is a temperature scale of vulnerability of materials and inhibition of corrosion by certain factors at within the atmospheric distillation column of crude oil.</p></sec></sec><sec id="s3_3"><title>3.3. Activity Zone of Corrosion Factors in the Atmospheric Distillation Column</title><p><xref ref-type="fig" rid="fig3">Figure 3</xref> shows the distribution of the activity of the corrosion factors as a function of the temperature of the medium. The bright colors show the maximum activity of the corrosion factors in the distillation column, the lighter the color</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Temperature scale of vulnerability and inhibition of corrosion by certain corrosion factors in the atmospheric distillation column</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Type of corrosion</th><th align="center" valign="middle" >Vulnerability temperatures</th><th align="center" valign="middle" >Corrosion inhibitor temperatures</th></tr></thead><tr><td align="center" valign="middle" >Naphtaline corrosion</td><td align="center" valign="middle" >493 - 673 K</td><td align="center" valign="middle" >&gt;673 K</td></tr><tr><td align="center" valign="middle" >Sulfur compounds corrosion</td><td align="center" valign="middle" >503 - 698 K</td><td align="center" valign="middle" >&gt;425 K</td></tr><tr><td align="center" valign="middle" >Dioxide carbon corrosion</td><td align="center" valign="middle" >&lt;343 K</td><td align="center" valign="middle" >&gt;343 K</td></tr></tbody></table></table-wrap><p>becomes, the more the vulnerability decreases. The red color represents corrosion by sulfur compounds; blue represents corrosion by carbon dioxide, orange corrosion by naphthenic acids distributed in the various petroleum cuts of the atmospheric distillation column.</p><p>In addition, the time parameter in the evolution of the mass loss would make it possible to evaluate the lifetime of the materials thus undergoing corrosion in the atmospheric distillation system.</p></sec></sec><sec id="s4"><title>4. Conclusion</title><p>The overall objective of this study was to define a temperature scale for understanding the corrosion mechanisms in the corrosion control process in the atmospheric distillation column. This work has shown that for the main corrosion factor compounds in the atmospheric distillation column there is a temperature scale of vulnerability and a temperature beyond which, corrosion is inhibited. Therefore, corrosion does not increase exponentially with temperature. The time parameter, which is also linked to the mass loss, could help to predict the lifespan of materials. In perspective in the fight against corrosion in the atmospheric distillation system, these results would permit to redefine certain methods of fighting and inhibiting corrosion based on the temperature parameter in order to reduce the significant cost of corrosion in the refining industry. In addition, it would be interesting to conduct a study in the different units of the atmospheric distillation system in order to choose the appropriate metal according to the operating temperature and the content of the crude products in corrosion factors.</p></sec><sec id="s5"><title>Acknowledgements</title><p>N. F. thanks Dahibou fall SOW mathematical and numerical engineer at the Mathematical Department at Cheikh Anta DIOP university of DAKAR-SENEGAL.</p></sec><sec id="s6"><title>Conflicts of Interest</title><p>The authors declare no conflicts of interest regarding the publication of this paper.</p></sec><sec id="s7"><title>Cite this paper</title><p>Fall, N., Diop, D., Ndiaye, S., Talla, K., Adannou, H.A., Sarr, A. and Beye, A.C. (2023) Modeling and Study Influence of the Temperature Parameter on Corrosion Factors in the Atmospheric Distillation Column of Crude Oil. Open Journal of Yangtze Gas and Oil, 8, 1-10. https://doi.org/10.4236/ojogas.2023.81001</p></sec></body><back><ref-list><title>References</title><ref id="scirp.122363-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Bradford, S. (1993) Corrosion Control. Van Nostrand Reinhold, New York.</mixed-citation></ref><ref id="scirp.122363-ref2"><label>2</label><mixed-citation publication-type="other" xlink:type="simple">Thierry, M. (2000) Corrosion of Carbon Steel in Crude Oils Containing Naphtenic Acids: Determination of Methods for Evaluation of Instaneous Corrosion Rate. Ph.D. Dissertation, National Institute of Applied Sciences of Lyon (Doctoral School of Materials of Lyon), Lyon.</mixed-citation></ref><ref id="scirp.122363-ref3"><label>3</label><mixed-citation publication-type="other" xlink:type="simple">Dewaard, C., Lotz, U. and Milliams, D.E. (1991) Predictives Model for CO2 Corrosion Ingineering in Wel Natural Gas Pipelines. Corrosion, 47, 976-985. https://doi.org/10.5006/1.3585212</mixed-citation></ref><ref id="scirp.122363-ref4"><label>4</label><mixed-citation publication-type="book" xlink:type="simple">Groysman, A. (2017) Corrosion Problems and Solutions in Oil Refining and Petrochemical Industry. In: Gheorghe, A.V., Ed., Topic in Safety, Risk, and Quality, Old Dominion University, Norfolk, 38-42. https://doi.org/10.1007/978-3-319-45256-2</mixed-citation></ref><ref id="scirp.122363-ref5"><label>5</label><mixed-citation publication-type="other" xlink:type="simple">Al-Moubaraki, A.H. and Obot, I.B. (2021) Corrosion Challenges in Petroleum Refinery Operations: Sources, Mechanisms, Mitigation, and Future Outlook. Journal of Saudi Chemical Society, 25, Article ID: 101370. https://doi.org/10.1016/j.jscs.2021.101370</mixed-citation></ref><ref id="scirp.122363-ref6"><label>6</label><mixed-citation publication-type="other" xlink:type="simple">Ropital, Fr. (2009) Corrosion and Degradation of Metallic Materials: Understanding Phenomena and Applications in the Petroleum Industry and Processes. TECHNIP Edition, Paris, 3-14.</mixed-citation></ref><ref id="scirp.122363-ref7"><label>7</label><mixed-citation publication-type="other" xlink:type="simple">API RP 939-C (2008) Guidelines for Avoiding Sulfidation (Sulfidic) Corrosion Failures in Oil Refineries. American Petroleum Institute, Washington DC.</mixed-citation></ref><ref id="scirp.122363-ref8"><label>8</label><mixed-citation publication-type="other" xlink:type="simple">Lyons, E., Plisga, G.T. and Lorentz, M. (2015) Standard Handbook of Petroleum and Natural Gas. Third Edition, Gulf Professional Publishing, Oxford, 1822 p.</mixed-citation></ref><ref id="scirp.122363-ref9"><label>9</label><mixed-citation publication-type="other" xlink:type="simple">Nesic, S. (2007) Key Issues Related to Modelling of Internal Corrosion of Oil and Gas Pipelines—A Review. Corrosion Science, 49, 4308-4338. https://doi.org/10.1016/j.corsci.2007.06.006</mixed-citation></ref><ref id="scirp.122363-ref10"><label>10</label><mixed-citation publication-type="other" xlink:type="simple">Fadhil, A.A., et al. (2019) Ceramics Coating Materials for Corrosion Control of Crude Oil Distillation Column: Experimental and Theoretical Studies. Corrosion Science, 162, Article ID: 108220. https://doi.org/10.1016/j.corsci.2019.108220</mixed-citation></ref><ref id="scirp.122363-ref11"><label>11</label><mixed-citation publication-type="other" xlink:type="simple">Khadom, A.A., Yaro, A.S., Altaie, A.S. and Musa, A.Y. (2009) The Effect of Temperature and Acid Concentration on Corrosion of Low Carbon Steel in Hydrochloric Acid Media. American Journal of Applied Sciences, 6, 1403-1409. https://doi.org/10.3844/ajassp.2009.1403.1409</mixed-citation></ref><ref id="scirp.122363-ref12"><label>12</label><mixed-citation publication-type="other" xlink:type="simple">Fadhil, A.A., Ismael, M.H., Farhan, S.N., Khadom, A.A., Liu, H. and Fu, Ch. (2018) Corrosion of Crude Oil Distillation Column: Kinetics and Mathematical View. Springer, Berlin, 1-8. https://doi.org/10.1007/s40735-019-0272-2</mixed-citation></ref><ref id="scirp.122363-ref13"><label>13</label><mixed-citation publication-type="other" xlink:type="simple">Yaro, A.S., Al-Jendeel, H. and Khadom, A.A. (2011) Cathodic Protection System of Copper-Zinc-Saline Water in Presence of Bacteria. Desalination, 270, 193-198. https://doi.org/10.1016/j.desal.2010.11.045</mixed-citation></ref><ref id="scirp.122363-ref14"><label>14</label><mixed-citation publication-type="other" xlink:type="simple">Mahmood, A.K. and Khadom, A.A. (2016) Erosion-Corrosion of Low-Carbon Steel in the Absence and Presence of Slurry in Saline Water: Kinetic and Mathematical Views. Journal of Failure Analysis and Prevention, 16, 1071-1081. https://doi.org/10.1007/s11668-016-0180-4</mixed-citation></ref><ref id="scirp.122363-ref15"><label>15</label><mixed-citation publication-type="other" xlink:type="simple">Emmanuel, S. (2015) Corrosion Behavior of Commercial Metal Materials and Models under Typical Conditions UVEOM. Ph.D. Dissertation, Lorraine University, Lorraine.</mixed-citation></ref></ref-list></back></article>