<?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">JMMCE</journal-id><journal-title-group><journal-title>Journal of Minerals and Materials Characterization and Engineering</journal-title></journal-title-group><issn pub-type="epub">2327-4077</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/jmmce.2016.41004</article-id><article-id pub-id-type="publisher-id">JMMCE-62818</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Chemistry&amp;Materials Science</subject><subject> Engineering</subject></subj-group></article-categories><title-group><article-title>
 
 
  Investigation of &lt;i&gt;Aloe lateritia&lt;/i&gt; Gel as Corrosion Inhibitor for Mild Steel in 2 M HNO&lt;sub&gt;3&lt;/sub&gt; and 1 M H&lt;sub&gt;2&lt;/sub&gt;SO&lt;sub&gt;4&lt;/sub&gt; Media
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>ucas</surname><given-names>Paul</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>Revocatus</surname><given-names>L. Machunda</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib></contrib-group><aff id="aff2"><addr-line>Department of Water and Environmental Science and Engineering, Nelson Mandela African Institution of
Science and Technology, Arusha, Tanzania</addr-line></aff><aff id="aff1"><addr-line>Department of Materials and Energy Science &amp;amp; Engineering, Nelson Mandela African Institution of Science
and Technology, Arusha, Tanzania</addr-line></aff><author-notes><corresp id="cor1">* E-mail:<email>paull@nm-aist.ac.tz(UP)</email>;</corresp></author-notes><pub-date pub-type="epub"><day>13</day><month>01</month><year>2016</year></pub-date><volume>04</volume><issue>01</issue><fpage>33</fpage><lpage>39</lpage><history><date date-type="received"><day>5</day>	<month>December</month>	<year>2015</year></date><date date-type="rev-recd"><day>accepted</day>	<month>15</month>	<year>January</year>	</date><date date-type="accepted"><day>18</day>	<month>January</month>	<year>2016</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>
 
 
  Corrsion inhibition of Aloe lateritia gel for Mild steel in 2 M HNO
  <sub>3</sub> and 1 M H
  <sub>2</sub>SO
  <sub>4</sub> solutions was investigated by potentiodynamic polarization, Scanning electron microscopy (SEM) and Foutier transform infrared (FT-IR). Inhibition efficiency increased with the increase of the concentration of the gel. The optimal concentration of the gel gives maximum inhibition efficiency of 77.4% and 70.3% in 1 M H
  <sub>2</sub>SO
  <sub>4</sub> and 2 M HNO
  <sub>3</sub> respectively. Polarization plots shows that, the gel works as a mixed type inhibitor altering both cathodic and anodic reaction. SEM proves the uniform and pitting corrosion at the surface of Mild steel in 1 M H
  <sub>2</sub>SO
  <sub>4</sub> and 2 M HNO
  <sub>3</sub> respectively. Using FT-IR potential function groups from pure gel and some stretch shift was observed from corrosion product and some stretch shift from corrosion products was observed.
 
</p></abstract><kwd-group><kwd>Corrosion Inhibitor</kwd><kwd> Mild Steel</kwd><kwd> Potentiodynamic Polarization</kwd><kwd> Sulfuric Acid</kwd><kwd> Nitric Acid</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Mild steel is popular in the construction of different structures like pipelines, thermal chemical reactor and cooling system, since it is excellent in performance, highly recyclable, high life span, strength as well as more ductile [<xref ref-type="bibr" rid="scirp.62818-ref1">1</xref>] .</p><p>Corrosion is the catastrophic deterioration of material’s properties due to electrochemical reaction caused by potential differences between the oxidant (corrosive medium) and reductant (metals). The external energy absorbed by the metal during their extraction is the driving forces to return to their stable oxidation state (ores) by corrosion, since always exist in the temporary unstable state.</p><p>Mild steel suffers from corrosion when exposed acidic medium. For this study 2 M HNO<sub>3</sub> and 1 M H<sub>2</sub>SO<sub>4</sub> is going to be used as the corrosion medium. Nitric acid participates during corrosion by cathodic reactions:</p><disp-formula id="scirp.62818-formula375"><label>(1)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/4-2710393x7.png"  xlink:type="simple"/></disp-formula><disp-formula id="scirp.62818-formula376"><label>(2)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/4-2710393x8.png"  xlink:type="simple"/></disp-formula><disp-formula id="scirp.62818-formula377"><label>(3)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/4-2710393x9.png"  xlink:type="simple"/></disp-formula><disp-formula id="scirp.62818-formula378"><label>(4)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/4-2710393x10.png"  xlink:type="simple"/></disp-formula><disp-formula id="scirp.62818-formula379"><label>(5)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/4-2710393x11.png"  xlink:type="simple"/></disp-formula><p>Interaction between nitrous acid (HNO<sub>2</sub>) from Equation (4) and nitric acid (HNO<sub>3</sub>) produces nitrogen dioxide (NO<sub>2</sub>).</p><disp-formula id="scirp.62818-formula380"><label>(6)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/4-2710393x12.png"  xlink:type="simple"/></disp-formula><p>Finally the cathodic reaction becomes autocatalytic, where NO<sub>2</sub> combine with ammonium (NH<sub>3</sub>) to produce ammonium salt (NH<sub>4</sub>NO<sub>2</sub>) and (NH<sub>4</sub>NO<sub>3</sub>) which finally decomposes to give nitrogen gas (N<sub>2</sub> (g)) and nitrogen oxides. These products are accompanied by brown gas evolution.</p><disp-formula id="scirp.62818-formula381"><label>(7)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/4-2710393x13.png"  xlink:type="simple"/></disp-formula><disp-formula id="scirp.62818-formula382"><label>(8)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/4-2710393x14.png"  xlink:type="simple"/></disp-formula><p>As reported by [<xref ref-type="bibr" rid="scirp.62818-ref2">2</xref>] .</p><p>Sulphuric acid is the most used chemicals in almost every industry like in petroleum production, fertilizer manufacture, paint production, metal pickling and extraction of non-metals [<xref ref-type="bibr" rid="scirp.62818-ref3">3</xref>] .</p><p>Major challenge with acid like H<sub>2</sub>SO<sub>4</sub> and HNO<sub>3</sub> they accelerate corrosion in several equipments, so there is a need to be inhibited. There are several methods has been used to control and prevent corrosion. However, use of corrosion inhibitor is more effective, especially in corrosion enhanced by acid. Inhibitor performs well due to ability to create a barrier for interaction between the materials and the medium. This is due to presence of electrons rich functional groups and atom like Oxygen (O), Sulpher (S), Nitrogen (N) and the multiple bonds in their conjugate system [<xref ref-type="bibr" rid="scirp.62818-ref4">4</xref>] .</p><p>Synthetic corrosion inhibitors used for several years have been reported to be unfriendly to the environment; therefore, searching for green ones is inevitable. Compounds from plants recently have been recognized to be the best eco-friendly inhibitors [<xref ref-type="bibr" rid="scirp.62818-ref5">5</xref>] - [<xref ref-type="bibr" rid="scirp.62818-ref8">8</xref>] .</p><p>This study intends to investigate the insight about corrosion of Mild steel in 1 M H<sub>2</sub>SO<sub>4</sub> and 2 M HNO<sub>3</sub> in presence of Aloe lateritia gel. The use of Aloe lateritia gels as corrosion inhibitor has been hardly reported. The inhibitory effect of these naturally occurring plant gels on corrosion of Mild steel in 1M H<sub>2</sub>SO<sub>4</sub> and 2 M HNO<sub>3</sub> was investigated by potentiodynamic polarization. Additionally, surface analysis was obtained from SEM. FT-IR was used to identify functional groups from the gels and that of corrosion products from metals which were inhibited.</p><p>Potentiodynamic polarization was used to control the electrochemical reaction of corrosion by monitoring Anodic and Cathodic reactions:</p><disp-formula id="scirp.62818-formula383"><label>(9)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/4-2710393x15.png"  xlink:type="simple"/></disp-formula><disp-formula id="scirp.62818-formula384"><label>(10)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/4-2710393x16.png"  xlink:type="simple"/></disp-formula><p>This is useful to determine the corrosion rate, passivation especially the region where metal is active and noble. It helps to determine pitting tendency of metal during corrosion reaction. The overall reaction produces the anodic current, for uninhibited system produces more current as compared to inhibited; due to high dissolution of metal. The expression below in Equation (11) uses the current to determine the inhibition efficiency when inhibitor is used [<xref ref-type="bibr" rid="scirp.62818-ref9">9</xref>] .</p><disp-formula id="scirp.62818-formula385"><label>(11)</label><graphic position="anchor" xlink:href="http://html.scirp.org/file/4-2710393x17.png"  xlink:type="simple"/></disp-formula><p>where %IE is inhibition efficiency, <inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/4-2710393x18.png" xlink:type="simple"/></inline-formula>and i<sub>corr</sub> are corrosion current densities of unhibited and inhibited solutions respectively.</p><p>To determine extend of corrosion, SEM was used to monitor the level of deterioration of the metal surface. Inhibited metal expected to have a smooth surface comparatively with uninhibited; this is due to fact that inhibitor prevents interaction of the metal and the surrounding medium [<xref ref-type="bibr" rid="scirp.62818-ref10">10</xref>] . FT-IR was used to determine function groups of the inhibitor before and after being applied therefore, obtained corrosion product has comparable functional groups to that of inhibitor; this is along with that reported by [<xref ref-type="bibr" rid="scirp.62818-ref11">11</xref>] .</p></sec><sec id="s2"><title>2. Materials and Methods</title><sec id="s2_1"><title>2.1. Sample Preparation</title><p>2 M HNO<sub>3</sub> and 1 M H<sub>2</sub>SO<sub>4</sub> was prepared by diluting 69% HNO<sub>3</sub> and 98% H<sub>2</sub>SO<sub>4 </sub>with distilled water as corrosive medium. Plant inhibitor Aloe lateritia gel was obtained from the western part of Kahama district at Wendere village, Tanzania. The gel was obtained by cutting the leaves and squeezing, then filtering through the mesh of cloth to get pure gel. About 1 kg of fresh leaves was used to obtain 2 Litters of gel. It was kept cool in a refrigerator prior to testing this is, in similar to what reported by [<xref ref-type="bibr" rid="scirp.62818-ref12">12</xref>] . Concentration of inhibitors: (0%, 3.2%, 6.3%, 9.1%, 11.8%, 14.3% v/v) was used at room temperature.</p><p>Mild steel with following composition was used: C―0.15, Mn―1.26, V―0.017, Si―0.035, S―0.008, Cr―0.036, Ni―0.03, Al―0.083, Cu―0.038 and the remainder is Fe. The metal was cut into 2 cmx1 cm as working electrode for electrochemical measurements. The surface of metal was pre-cleaned using silicon carbide paper; it was made to silver mirror by cleaning using diamond paste. Finally, by using acetone and distilled water in an utrasonicator bath was washed and rinsed then stored for use.</p></sec><sec id="s2_2"><title>2.2. Potentiodynamic Polarization</title><p>The experiment was performed in a conversational cell with three electrodes connected to a potentiostat (PGSTAT 302N). Mild steel was used as working electrode in 2 M HNO<sub>3</sub> and 1 M H<sub>2</sub>SO<sub>4</sub> corrosive medium. Platinum wire, saturated calomel electrode was used as a counter and reference electrodes respectively. The plots used to obtain the tafel curve were done by changing the potential from −250 to +250 mV at scan rate of 1mV∙s<sup>−1</sup> against open circuit potential.</p></sec><sec id="s2_3"><title>2.3. SEM for Surface Morphology Analysis</title><p>The surface of Mild steel exposed to uninhibited 2 M HNO<sub>3</sub> and 1 M H<sub>2</sub>SO<sub>4</sub> and to that containing optimal concentration of inhibitor, was examined by Field Scanning Electron Microscope (FE-SEM, Hilachi, S-4700). Before exposing to SEM the metal was cleaned thoroughly to remove the oxide layer and after 24 hours prior-o to measurement was washed using running distilled water and dried. Corrosion products were obtained by removing the oxide surface of the metal using the utrasonicator, and then were submitted for measurement.</p></sec><sec id="s2_4"><title>2.4. FTIR for Functional Group Identification</title><p>The inhibitor gels and the corrosion products were subjected to Varian 660-IR for the determination of appropriate functional groups available. Few drops of Aloe lateritia gel and the corrosion products obtained after 24 hours of metal corrosion in optimal inhibitor were subjected to FTIR measurements.</p></sec></sec><sec id="s3"><title>3. Results and Discussion</title><sec id="s3_1"><title>3.1. Potentiodynamic Polarization</title><p>It was used to obtain polarization curves for the Mild steel in 2 M HNO<sub>3</sub> and 1 M H<sub>2</sub>SO<sub>4</sub> with and without the addition of Aloe lateritia gel.</p><p>The plots from <xref ref-type="fig" rid="fig1">Figure 1</xref> and <xref ref-type="fig" rid="fig2">Figure 2</xref> reveal that Tafel plot was obeyed by anodic and cathodic reactions. The linear part of the Tafel plots were extrapolated, at the point of intersection is where corrosion potential (E<sub>corr</sub>)</p><fig id="fig1"  position="float"><label><xref ref-type="fig" rid="fig1">Figure 1</xref></label><caption><title> Polarization curves of mild steel in 2 M HNO<sub>3</sub> in presence with different concentration of Aloe lateritia gel</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/4-2710393x19.png"/></fig><fig id="fig2"  position="float"><label><xref ref-type="fig" rid="fig2">Figure 2</xref></label><caption><title> Polarization curves of mild steel in 1 M H<sub>2</sub>SO<sub>4</sub> with different concentration of Aloe lateritia gels</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/4-2710393x20.png"/></fig><p>and corrosion current density (i<sub>corr</sub>) were obtained.</p><p>Related parameters like Cathodic Tafel slope (b<sub>c</sub>), anodic Tafel slope (b<sub>a</sub>), corrosion current density (i<sub>corr</sub>) and corrosion potential (E<sub>corr</sub>) were calculated and results are tablated in <xref ref-type="table" rid="table1">Table 1</xref>.</p><p>An increase in the concentration of inhibitor resulted in the following:</p><p>There is equal shift for the potential toward more negative and positive relating to cathodic and anodic respectively; this indicates that reaction mechanism was the same. From <xref ref-type="table" rid="table1">Table 1</xref> it is observed that there is a decrease of corrosion current density (i<sub>corr</sub>) contrary to inhibitor concentration. This is attributed by the ability of inhibitor to prevent interaction between metal and the corrosive medium which leads to corrosion. Although, the corrosion current density (i<sub>corr</sub>) decrease as inhibitor’s concentration increases; no remarkable shift of corrosion potential (E<sub>corr</sub>) was observed. This is to say a mixed type inhibition for both anodic and cathodic reactions took place, the observation is associated with that reported by [<xref ref-type="bibr" rid="scirp.62818-ref13">13</xref>] .</p><p>Inhibition efficiency (%IE) was obtained by Equation (11) when the concentration of inhibitor increased %IE increases too. From <xref ref-type="table" rid="table1">Table 1</xref> at 14.3% v/v of inhibitor %IE reached maximum 77.4% for 1M H<sub>2</sub>SO<sub>4</sub> while for 2M HNO<sub>3</sub>%IE increased with concentration of inhibitor up to 11.8%v/v which attained 70.3%, then started to decrease as concentration increased. So the inhibitor performs better with H<sub>2</sub>SO<sub>4</sub> than HNO<sub>3</sub>.</p></sec><sec id="s3_2"><title>3.2. Surface Morphology</title><p>Mild steel was exposed to 1M H<sub>2</sub>SO<sub>4</sub> and 2M HNO<sub>3</sub> medium in the absence and presence of optimal amount</p><p>Aloe lateritia gel for 24 hours at room temperature. Their morphology was determined by SEM, the results from <xref ref-type="fig" rid="fig3">Figure 3</xref>(a) and <xref ref-type="fig" rid="fig3">Figure 3</xref>(c) verifies that the steel more corroded as the surface was more rough in blank medium. However, <xref ref-type="fig" rid="fig3">Figure 3</xref>(b) and <xref ref-type="fig" rid="fig3">Figure 3</xref>(d) is for the steel which was exposed in a corrosive medium with optimal concentrations of inhibitor.</p><p>The presence of inhibitor reduced the extent of corrosion, the surface become smoother compared to the uninhibited. This reveals the performance of inhibitor by protective layer formation; which separates the interaction between the metal and corrosive medium similar behavior observed by [<xref ref-type="bibr" rid="scirp.62818-ref14">14</xref>] . From <xref ref-type="fig" rid="fig3">Figure 3</xref>(a) and <xref ref-type="fig" rid="fig3">Figure 3</xref>(c) the metal exposed to blank 1 M H<sub>2</sub>SO<sub>4</sub> and 2 M HNO<sub>3</sub> displayed uniform and pitting corrosion respectively.</p></sec><sec id="s3_3"><title>3.3. FT-IR Analysis</title><p>For determination of the functional groups few drops of Aloe lateritia gel and that of corrosion products was used. The results were displayed for FT-IR spectrum as shown in <xref ref-type="fig" rid="fig4">Figure 4</xref>.</p><p>Aloe lateritia gel and that of corrosion product was exposed to IR spectrum and the results are shown in <xref ref-type="fig" rid="fig4">Figure 4</xref>(a) and <xref ref-type="fig" rid="fig4">Figure 4</xref>(b). The stretch for O-H which was around 3339.60 cm<sup>−1</sup> was shifted to 3360.29 cm<sup>−1</sup>, from 1635.49 cm<sup>−1</sup> to 1641.08 cm<sup>−1</sup> for C=C when the pure inhibitor gel and corrosion product respectively. The presence of stretch at 551.87 cm<sup>−1</sup> indicates presence of g-Fe<sub>2</sub>O<sub>3</sub> this verifies the interaction between the inhibitor and the metal surface was also observed as shown in <xref ref-type="table" rid="table2">Table 2</xref> [<xref ref-type="bibr" rid="scirp.62818-ref15">15</xref>] .</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Potentiodynamic polarization parameters for Mild steel in 2 M HNO<sub>3</sub> and 1 M H<sub>2</sub>SO<sub>4</sub></title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Acid medium</th><th align="center" valign="middle" >Extract concentration (%v/v)</th><th align="center" valign="middle" >E<sub>corr</sub> (Mv/SCE)</th><th align="center" valign="middle" >I<sub>corr</sub> (&#181;A∙cm<sup>−2</sup>)</th><th align="center" valign="middle" >b<sub>c</sub> (mV∙dec<sup>−1</sup>)</th><th align="center" valign="middle" >b<sub>a</sub> (mV∙dec<sup>−1</sup>)</th><th align="center" valign="middle" >%IE</th></tr></thead><tr><td align="center" valign="middle"  rowspan="6"  >H<sub>2</sub>SO<sub>4</sub></td><td align="center" valign="middle" >2 M H<sub>2</sub>SO<sub>4</sub></td><td align="center" valign="middle" >−0.1368</td><td align="center" valign="middle" >3.25 &#215; 10<sup>−06</sup></td><td align="center" valign="middle" >−1.3363</td><td align="center" valign="middle" >0.1252</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >3.2</td><td align="center" valign="middle" >−0.1170</td><td align="center" valign="middle" >1.84 &#215; 10<sup>−06</sup></td><td align="center" valign="middle" >−1.1848</td><td align="center" valign="middle" >0.1106</td><td align="center" valign="middle" >43.3</td></tr><tr><td align="center" valign="middle" >6.3</td><td align="center" valign="middle" >−0.1183</td><td align="center" valign="middle" >9.74 &#215; 10<sup>−07</sup></td><td align="center" valign="middle" >0.2715</td><td align="center" valign="middle" >0.0855</td><td align="center" valign="middle" >70.1</td></tr><tr><td align="center" valign="middle" >9.1</td><td align="center" valign="middle" >−0.1161</td><td align="center" valign="middle" >8.64 &#215; 10<sup>−07</sup></td><td align="center" valign="middle" >0.2811</td><td align="center" valign="middle" >0.0881</td><td align="center" valign="middle" >73.4</td></tr><tr><td align="center" valign="middle" >11.8</td><td align="center" valign="middle" >−0.1158</td><td align="center" valign="middle" >9.00 &#215; 10<sup>−07</sup></td><td align="center" valign="middle" >0.2359</td><td align="center" valign="middle" >0.0809</td><td align="center" valign="middle" >72.3</td></tr><tr><td align="center" valign="middle" >14.3</td><td align="center" valign="middle" >−0.1161</td><td align="center" valign="middle" >7.35 &#215; 10<sup>−07</sup></td><td align="center" valign="middle" >0.0679</td><td align="center" valign="middle" >0.2340</td><td align="center" valign="middle" >77.4</td></tr><tr><td align="center" valign="middle"  rowspan="6"  >HNO<sub>3</sub></td><td align="center" valign="middle" >1 M HNO<sub>3</sub></td><td align="center" valign="middle" >0.0745</td><td align="center" valign="middle" >2.38 &#215; 10<sup>−06</sup></td><td align="center" valign="middle" >0.3903</td><td align="center" valign="middle" >0.22058</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >3.2</td><td align="center" valign="middle" >0.0831</td><td align="center" valign="middle" >8.38 &#215; 10<sup>−07</sup></td><td align="center" valign="middle" >0.1948</td><td align="center" valign="middle" >0.21413</td><td align="center" valign="middle" >64.8</td></tr><tr><td align="center" valign="middle" >6.3</td><td align="center" valign="middle" >0.0746</td><td align="center" valign="middle" >7.69 &#215; 10<sup>−07</sup></td><td align="center" valign="middle" >0.1965</td><td align="center" valign="middle" >0.20044</td><td align="center" valign="middle" >67.7</td></tr><tr><td align="center" valign="middle" >9.1</td><td align="center" valign="middle" >0.1124</td><td align="center" valign="middle" >7.30 &#215; 10<sup>−07</sup></td><td align="center" valign="middle" >0.1508</td><td align="center" valign="middle" >0.17174</td><td align="center" valign="middle" >69.4</td></tr><tr><td align="center" valign="middle" >11.8</td><td align="center" valign="middle" >0.1156</td><td align="center" valign="middle" >7.09 &#215; 10<sup>−07</sup></td><td align="center" valign="middle" >0.1201</td><td align="center" valign="middle" >0.11627</td><td align="center" valign="middle" >70.3</td></tr><tr><td align="center" valign="middle" >14.3</td><td align="center" valign="middle" >0.1393</td><td align="center" valign="middle" >7.27 &#215; 10<sup>−07</sup></td><td align="center" valign="middle" >0.1353</td><td align="center" valign="middle" >0.16888</td><td align="center" valign="middle" >69.5</td></tr></tbody></table></table-wrap><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> Different frequencies of IR spectrum of corrosion product and pure Aloe lateritia gel</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  colspan="2"  >Pure extracts</th><th align="center" valign="middle"  colspan="2"  >Corrosion products</th></tr></thead><tr><td align="center" valign="middle" >Frequencies (cm<sup>−1</sup>)</td><td align="center" valign="middle" >Assignment</td><td align="center" valign="middle" >Frequencies (cm<sup>−1</sup>)</td><td align="center" valign="middle" >Assignment</td></tr><tr><td align="center" valign="middle" >3339.60</td><td align="center" valign="middle" >O-H</td><td align="center" valign="middle" >3360.29</td><td align="center" valign="middle" >O-H</td></tr><tr><td align="center" valign="middle" >1635.49</td><td align="center" valign="middle" >C=C</td><td align="center" valign="middle" >1641.08</td><td align="center" valign="middle" >C=C</td></tr><tr><td align="center" valign="middle" >2110.25</td><td align="center" valign="middle" >C&#186;C</td><td align="center" valign="middle" >1339.45</td><td align="center" valign="middle" >C-H rock</td></tr><tr><td align="center" valign="middle" >1275.68</td><td align="center" valign="middle" >C-O-C</td><td align="center" valign="middle" >551.87</td><td align="center" valign="middle" >g-Fe<sub>2</sub>O<sub>3</sub></td></tr></tbody></table></table-wrap><fig id="fig3"  position="float"><label><xref ref-type="fig" rid="fig3">Figure 3</xref></label><caption><title> SEM micrographs of mild steel surface exposed in (a) 1 M H<sub>2</sub>SO<sub>4</sub> solution (b) 1 M H<sub>2</sub>SO<sub>4</sub> with 14.3 (%v/v) Aloe lateritia gel; (c) 2 M HNO<sub>3</sub> solution and (d) 2 M HNO<sub>3</sub> with 11.8 (%v/v) Aloe lateritia gel at room temperature for 24 hours</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/4-2710393x21.png"/></fig><fig-group id="fig4"><label><xref ref-type="fig" rid="fig4">Figure 4</xref></label><caption><title> FT-IR spectrum for the (a) pure Aloe lateritia gel and (b) corrsion products respectively.</title></caption><fig id ="fig4_1"><label>(b)</label><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/4-2710393x22.png"/></fig><fig id ="fig4_2"><label></label><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/4-2710393x23.png"/></fig></fig-group></sec></sec><sec id="s4"><title>4. Conclusion</title><p>The inhibitor gel was observed to perform well on both H<sub>2</sub>SO<sub>4</sub> and HNO<sub>3</sub> medium. Inhibition efficiencies were observed to rise with a concentration of inhibitor. Maximum efficiencies of 77.4% at 14.3% v/v for 1 M H<sub>2</sub>SO<sub>4</sub> and 70.3% at 11.8% v/v for 2 M HNO<sub>3</sub> were noticed. Mixed type of inhibition was revealed since no remarkable shift of E<sub>corr</sub>. SEM images revealed effective performance of inhibitor since inhibited metal appeared to be smoother than uninhibited. FT-IR information’s proved the interaction between inhibitor and metal surfaces. Additionally the functional groups stretch shift and decrease of I<sub>corr</sub> proves the film formation and lowering metal dissolution.</p></sec><sec id="s5"><title>Acknowledgements</title><p>This work was supported by British Gas (BG) scholarship for my studies at Nelson Mandela African Institution of Science and Technology (NM-AIST). I appreciate Dr. Kiseok Jung for proofreading this work.</p></sec><sec id="s6"><title>Cite this paper</title><p>LucasPaul,Revocatus L.Machunda, (2016) Investigation of Aloe lateritia Gel as Corrosion Inhibitor for Mild Steel in 2 M HNO<sub>3</sub> and 1 M H<sub>2</sub>SO<sub>4</sub> Media. Journal of Minerals and Materials Characterization and Engineering,04,33-39. doi: 10.4236/jmmce.2016.41004</p></sec><sec id="s7"><title>NOTES</title></sec></body><back><ref-list><title>References</title><ref id="scirp.62818-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Hmimou, J., Rochdi, A., Touir, R., Ebn Touhami, M., Rifi, E., El Hallaouti, A., Anouar, A and Chebab, D. (2012) Study of Corrosion Inhibition of Mild Steel in Acidic Medium by 2-Propargyl-5-p-Chlorophenyl&lt;br /&gt;tetrazole: Part I. Journal of Materials and Environmental Science, 3, 543-550.</mixed-citation></ref><ref id="scirp.62818-ref2"><label>2</label><mixed-citation publication-type="other" xlink:type="simple">Wiersma, B.J. (2002) Corrosion Testing of Carbon Steel in Acid Cleaning. Google Search [Online].   
&lt;br /&gt;https://www.google.co.tz/?gws_rd=ssl#q=corrosion+Testing+of+carbon+steel+in+acid+cleaning</mixed-citation></ref><ref id="scirp.62818-ref3"><label>3</label><mixed-citation publication-type="other" xlink:type="simple">Shankar Rao, V. and Singhal, L.K. (2008) Corrosion Behavior and Passive Film Chemistry of 216 L Stainless Steel in Sulphuric Acid. Journal of Materials Science, 44, 2327-2333. &lt;br /&gt;http://dx.doi.org/10.1007/s10853-008-2976-4</mixed-citation></ref><ref id="scirp.62818-ref4"><label>4</label><mixed-citation publication-type="other" xlink:type="simple">Umoren, S.A., Gasem, Z.M. and Obot, I.B. (2013) Natural Products for Material Protection: Inhibition of Mild Steel Corrosion by Date Palm Seed Extracts in Acidic Media. Industrial &amp; Engineering Chemistry Research, 52, 14855- 14865. http://dx.doi.org/10.1021/ie401737u</mixed-citation></ref><ref id="scirp.62818-ref5"><label>5</label><mixed-citation publication-type="other" xlink:type="simple">Bouyanzer, A., Hammouti, B. and Majidi, L. (2006) Pennyroyal Oil from Mentha pulegium as Corrosion Inhibitor for Steel in 1 M HCl. Materials Letters, 60, 2840-2843. &lt;br /&gt;http://dx.doi.org/10.1016/j.matlet.2006.01.103</mixed-citation></ref><ref id="scirp.62818-ref6"><label>6</label><mixed-citation publication-type="other" xlink:type="simple">Rahim, A.A., Rocca, E., Steinmetz, J. and Jain Kassim, M. (2008) Inhibitive Action of Mangrove Tannins and Phosphoric Acid on Pre-Rusted Steel via Electrochemical Methods. Corrosion Science, 50, 1546-1550.  
http://dx.doi.org/10.1016/j.corsci.2008.02.013</mixed-citation></ref><ref id="scirp.62818-ref7"><label>7</label><mixed-citation publication-type="other" xlink:type="simple">Chauhan, L.R. and Gunasekaran, G. (2007) Corrosion Inhibition of Mild Steel by Plant Extract in Dilute HCl Medium. Corrosion Science, 49, 1143-1161. http://dx.doi.org/10.1016/j.corsci.2006.08.012</mixed-citation></ref><ref id="scirp.62818-ref8"><label>8</label><mixed-citation publication-type="other" xlink:type="simple">Abdel-Gaber, M., Abd-El-Nabey, B.A., Sidahmed, I.M., El-Zayady, A.M. and Saadawy, M. (2006) Inhibitive Action of Some Plant Extracts on the Corrosion of Steel in Acidic Media. Corrosion Science, 48, 2765-2779.  
http://dx.doi.org/10.1016/j.corsci.2005.09.017</mixed-citation></ref><ref id="scirp.62818-ref9"><label>9</label><mixed-citation publication-type="other" xlink:type="simple">Principles, E. and Polarization, P. (1980) Application Note CORR-1 Basics of Corrosion Measurements. Princeton Applied Research.</mixed-citation></ref><ref id="scirp.62818-ref10"><label>10</label><mixed-citation publication-type="journal" xlink:type="simple"><name name-style="western"><surname>Zohdy</surname><given-names> K.M. </given-names></name>,<etal>et al</etal>. (<year>2015</year>)<article-title>Surface Protection of Carbon Steel in Acidic Solution Using Ethylenediam&lt;br /&gt;inetetraacetic Disodium Salt</article-title><source> International Journal of Electrochemical Science</source><volume> 10</volume>,<fpage> 414</fpage>-<lpage>431</lpage>.<pub-id pub-id-type="doi"></pub-id></mixed-citation></ref><ref id="scirp.62818-ref11"><label>11</label><mixed-citation publication-type="other" xlink:type="simple">Mohamed, W.A., Rateb, N.M. andShakour, A.A. (2004) Performance of Copper Corrosion Inhibitors in a Museum Environment—A Comparative Study Using FTIR Spectroscopy. Metal 04: Proceedings of the International Conference on Metals Conservation, Canberra, 4-8 October 2004, 369-378.</mixed-citation></ref><ref id="scirp.62818-ref12"><label>12</label><mixed-citation publication-type="other" xlink:type="simple">Hart, K. and James, A.O. (2014) Sabinet—The Inhibitive Effect of Aloe Vera Barbadensis Gel on Copper in Hydrochloric Acid Medium. Journal of Emerging Trends in Engineering and Applied Sciences, 5, 24-29.</mixed-citation></ref><ref id="scirp.62818-ref13"><label>13</label><mixed-citation publication-type="other" xlink:type="simple">Fouda, A.S., Attia, A.A. and Negm, A.A. (2014) Some Thiophene Derivatives as Corrosion Inhibitors for Carbon Steel in Hydrochloric Acid. Journal of Metallurgy, 2014, Article ID: 472040. &lt;br /&gt;http://dx.doi.org/10.1155/2014/472040</mixed-citation></ref><ref id="scirp.62818-ref14"><label>14</label><mixed-citation publication-type="other" xlink:type="simple">Kadhum, A.A.H., Mohamad, A.B., Hammed, L.A., Al-Amiery, A.A., San, N.H. and Musa, A.Y. (2014) Inhibition of Mild Steel Corrosion in Hydrochloric Acid Solution by New Coumarin. Materials, 7, 4335-4348.  
http://dx.doi.org/10.3390/ma7064335</mixed-citation></ref><ref id="scirp.62818-ref15"><label>15</label><mixed-citation publication-type="other" xlink:type="simple">Leelavathi, S. and Rajalakshmi, R. (2013) Dodonaea viscosa (L.) Leaves Extract as Acid Corrosion Inhibitor for Mild Steel—A Green Approach. Journal of Materials and Environmental Science, 4, 625-638.</mixed-citation></ref></ref-list></back></article>