<?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">MSCE</journal-id><journal-title-group><journal-title>Journal of Materials Science and Chemical Engineering</journal-title></journal-title-group><issn pub-type="epub">2327-6045</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/msce.2016.46005</article-id><article-id pub-id-type="publisher-id">MSCE-67486</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></subj-group></article-categories><title-group><article-title>
 
 
  Kinetics Study on Photocatalytic Degradation of Methyl Orange Catalyzed by Sea Urchin-Like Cu2O
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>R.</surname><given-names>J. Gao</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>T.</surname><given-names>Ding</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>X.</surname><given-names>J. Duan</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>Institutes of Materials Science and Engineering, Ocean University of China, Qingdao, China</addr-line></aff><aff id="aff2"><addr-line>Zaozhuang Vocational College of Science and Technology, Zaozhuang, China</addr-line></aff><pub-date pub-type="epub"><day>26</day><month>05</month><year>2016</year></pub-date><volume>04</volume><issue>06</issue><fpage>35</fpage><lpage>40</lpage><history><date date-type="received"><day>22</day>	<month>April</month>	<year>2016</year></date><date date-type="rev-recd"><day>accepted</day>	<month>15</month>	<year>June</year>	</date><date date-type="accepted"><day>20</day>	<month>June</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>
 
 
   Sea urchin-like cuprous oxide with hollow glass microsphere as core was prepared using sodium sulfite as the reducing agent and sodium acetate-acetic acid as buffer solution in copper sulfate solution. Methyl orange was selected as degradation target for photocatalytic experiments. The photocatalytic activities were investigated by visible spectro- photometer. Photocatalytic kinetics parameters were studied by the Langmuir-Hinshelwood model and Arrhenius formula. It was observed that the sea urchin-like morphology dramatically improved the photocatalytic activity of cuprous oxide. The photo-degradation belongs to the first-order reaction and the maximum degradation rate could reach 94.37%. The activation energy and pre-exponential factor are 41.18 KJ&#183;mol<sup>-1</sup> and 1.07 &#215; 10<sup>6</sup>, respectively. After seven times recycling, the sample still showed high photo-catalytic efficiency and stability. 
 
</p></abstract><kwd-group><kwd>Cuprous Oxide</kwd><kwd> Sea Urchin-Like</kwd><kwd> Photo-Catalyst</kwd><kwd> Reaction Kinetic</kwd><kwd> Methyl Orange</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Dye wastewater with the characteristics of complex composition, high color and emissions, high toxicity and poor biodegradability has serious polluted the environment. The common treatment methods of the dye wastewater are flocculation precipitation [<xref ref-type="bibr" rid="scirp.67486-ref1">1</xref>], electrolysis [<xref ref-type="bibr" rid="scirp.67486-ref2">2</xref>], adsorption [<xref ref-type="bibr" rid="scirp.67486-ref3">3</xref>], and biological vectors [<xref ref-type="bibr" rid="scirp.67486-ref4">4</xref>] in industry. One common disadvantage of these methods is that they can transfer the contamination from one phase to another rather than being destructive. Therefore, the invention of a new treatment method without secondary pollution is deemed necessary. In recent years, it has become a focus topic that catalyst is utilized to photodegrade the organic pollutants in wastewater. Cuprous oxide (Cu<sub>2</sub>O) has a direct band gap of 2.0 eV which can be excited by visible light, and it has high stability in solar cells [<xref ref-type="bibr" rid="scirp.67486-ref5">5</xref>]. In the past decade, Cu<sub>2</sub>O with various morphologies, such as nanosize spheres [<xref ref-type="bibr" rid="scirp.67486-ref6">6</xref>], sea urchin-like [<xref ref-type="bibr" rid="scirp.67486-ref7">7</xref>], porous octahedron [<xref ref-type="bibr" rid="scirp.67486-ref8">8</xref>], nanowires [<xref ref-type="bibr" rid="scirp.67486-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.67486-ref10">10</xref>], bi-pyra- mids [<xref ref-type="bibr" rid="scirp.67486-ref11">11</xref>] star-like and flower-like [<xref ref-type="bibr" rid="scirp.67486-ref12">12</xref>], has been synthesized by different techniques. Furthermore, it has showed an ideal effect on the photocatalytic degradation organic pollutants in water. However, there are rare reports on the photocatalytic kinetics of Cu<sub>2</sub>O in previous studies.</p><p>In this work, the influence of initial methyl orange (MO) concentration on photo-degradation efficiency was studied. Various kinetics parameters including the reaction rate constants, the activation energy, the pre-expo- nential factor and the reaction order were obtained and the stability property of the sea urchin-like Cu<sub>2</sub>O was also studied.</p></sec><sec id="s2"><title>2. Experimental</title><p>Preparation and characterization of the sea urchin-like Cu<sub>2</sub>O in detail has been investigated as in [<xref ref-type="bibr" rid="scirp.67486-ref7">7</xref>] and the SEM image of the sea urchin-like Cu<sub>2</sub>O shows in <xref ref-type="fig" rid="fig1">Figure 1</xref>. The sea urchin-like Cu<sub>2</sub>O of 0.50 g∙L<sup>−1</sup> was added into MO solutions with different initial concentrations according to the corresponding proportion. Then the system was illuminated under a 24 W fluorescent lamp (FSL) after the suspension was stirred in darkness for 40 min to ensure adsorption equilibrium. During the reaction, the beaker filled with the suspension was put into a water-bath to maintain the solution at a constant temperature. The distance between the lamp and the solution surface is 15 cm. The suspension was strongly stirred in order to keep the Cu<sub>2</sub>O well suspended in MO solution. During the course of irradiation, 10 mL of the suspension was drawn once from the mixture solution every 5 min and filtrated the Cu<sub>2</sub>O. The absorbance of MO aqueous solutions was measured by 7230 G visible spectrophotometer at 464 nm.</p></sec><sec id="s3"><title>3. Results and Discussion</title><sec id="s3_1"><title>3.1. Effect of Initial MO Concentration on Photodegradation Efficiency</title><p>As shown in <xref ref-type="fig" rid="fig2">Figure 2</xref> the degradation rate of MO first increases and then decreases with the increase of MO concentration from 20 mg∙L<sup>−1</sup> to 60 mg∙L<sup>−1</sup>. And the degradation rate of MO after 25 min reaches 90.9%, 92.23%, 94.37%, 91.48% and 35.35%, respectively.</p><fig id="fig1"  position="float"><label><xref ref-type="fig" rid="fig1">Figure 1</xref></label><caption><title>SEM image of the sea urchin-like Cu<sub>2</sub>O</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/67486x4.png"/></fig><fig id="fig2"  position="float"><label><xref ref-type="fig" rid="fig2">Figure 2</xref></label><caption><title> Effect of different initial MO concentration to the degradation rate</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/67486x5.png"/></fig><p>Compared with diffrentCu<sub>2</sub>O list in <xref ref-type="table" rid="table1">Table 1</xref>, sea urchin-like Cu<sub>2</sub>O showed much higher photocatalytic activity due to the three reasons. (a) Needle-like whiskers increase the surface area that determined by BET method is 3.3961 m<sup>2</sup>/g. While the BET surface areas of the octahedral morphology and the truncated octahedral morphology are 0.0308 m<sup>2</sup>/g and 0.1819 m<sup>2</sup>/g, respectively [<xref ref-type="bibr" rid="scirp.67486-ref13">13</xref>]. (b) The large area exposure of the Cu<sub>2</sub>O whiskers, in which visible light can occur numerous times of reflection and diffuse reflection, augments the adsorption ability and utilization rate of visible light. (c) The width size of crystal whiskers of the sea urchin-like Cu<sub>2</sub>O is only about 100 nm, so •OH species formed could easily reach the surface of the crystal whiskers to oxidize MO.</p></sec><sec id="s3_2"><title>3.2. Reaction Order of the Degradation of MO</title><p>The degradation of Cu<sub>2</sub>O to MO be supposed to first-order kinetics. So, the previous data (before 20 min) taken from <xref ref-type="fig" rid="fig2">Figure 2</xref> were drawn into plots of −ln(C/C<sub>0</sub>) and irradiation time shown in <xref ref-type="fig" rid="fig3">Figure 3</xref> The results reveal that the photo-degradation conform the pseudo first-order kinetics really.</p></sec><sec id="s3_3"><title>3.3. The Activation Energy (Ea) and Pre-Exponential Factor (A) of the Sea Urchin-Like Cu<sub>2</sub>O</title><p>The temperature can strongly increase the dye degradation, so the activation energy of degredation be studied by the Langmuir-Hinshelwood model [<xref ref-type="bibr" rid="scirp.67486-ref18">18</xref>]. <inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/67486x6.png" xlink:type="simple"/></inline-formula>OH<sup>−</sup> + h<sup>+</sup> → • OH, •OH + MO <inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/67486x7.png" xlink:type="simple"/></inline-formula> prod-</p><p>ucts. The degradation rate of MO be expressed as:<inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/67486x8.png" xlink:type="simple"/></inline-formula>. If irradiation time and the amount of</p><p>Cu<sub>2</sub>O are constant, the concentrations of •OH radicals are also constant, <inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/67486x9.png" xlink:type="simple"/></inline-formula>, then,<inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/67486x10.png" xlink:type="simple"/></inline-formula>. In</p><p>Arrhenius formula:<inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/67486x11.png" xlink:type="simple"/></inline-formula>, where, Ea is activation energy and A is pre-exponential factor. In Arrhenius formula:<inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/67486x12.png" xlink:type="simple"/></inline-formula>, where, Ea is activation energy and A is pre-exponential factor.</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> The degradation rate of MO in the presence of different Cu<sub>2</sub>O</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >MO (mg/L<sup>−1</sup>)</th><th align="center" valign="middle" >Cu<sub>2</sub>O (mg・L<sup>−1</sup>)</th><th align="center" valign="middle" >Time (min)</th><th align="center" valign="middle" >The degradation rate (%)</th><th align="center" valign="middle" >References</th></tr></thead><tr><td align="center" valign="middle" >40</td><td align="center" valign="middle" >2.00</td><td align="center" valign="middle" >70</td><td align="center" valign="middle" >83.49</td><td align="center" valign="middle" >Tang et al. [<xref ref-type="bibr" rid="scirp.67486-ref14">14</xref>]</td></tr><tr><td align="center" valign="middle" >20</td><td align="center" valign="middle" >0.20</td><td align="center" valign="middle" >420</td><td align="center" valign="middle" >65.5</td><td align="center" valign="middle" >Huang et al. [<xref ref-type="bibr" rid="scirp.67486-ref15">15</xref>]</td></tr><tr><td align="center" valign="middle" >10</td><td align="center" valign="middle" >1.00</td><td align="center" valign="middle" >60</td><td align="center" valign="middle" >62.5</td><td align="center" valign="middle" >Zhang et al. [<xref ref-type="bibr" rid="scirp.67486-ref16">16</xref>]</td></tr><tr><td align="center" valign="middle" >20</td><td align="center" valign="middle" >0.20</td><td align="center" valign="middle" >30</td><td align="center" valign="middle" >37</td><td align="center" valign="middle" >Sun et al. [<xref ref-type="bibr" rid="scirp.67486-ref17">17</xref>]</td></tr><tr><td align="center" valign="middle" >40</td><td align="center" valign="middle" >0.50</td><td align="center" valign="middle" >25</td><td align="center" valign="middle" >94.37</td><td align="center" valign="middle" >This work</td></tr></tbody></table></table-wrap><fig id="fig3"  position="float"><label><xref ref-type="fig" rid="fig3">Figure 3</xref></label><caption><title> First-order decay curve at different initial MO concentrations</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/67486x13.png"/></fig><p><xref ref-type="fig" rid="fig4">Figure 4</xref> shows the results of lnk at different temperature, lnk are given as:<inline-formula><inline-graphic xlink:href="http://html.scirp.org/file/67486x14.png" xlink:type="simple"/></inline-formula>.</p><p>Ea and A of the degradation are 41.18 KJ∙mol<sup>−1</sup> and 1.07 &#215; 10<sup>6</sup>, respectively, with the correlation coefficient of 0.997. Though the raction Ea is little higher than other Cu<sub>2</sub>O samples [<xref ref-type="bibr" rid="scirp.67486-ref13">13</xref>]-[<xref ref-type="bibr" rid="scirp.67486-ref15">15</xref>] [<xref ref-type="bibr" rid="scirp.67486-ref19">19</xref>]-[<xref ref-type="bibr" rid="scirp.67486-ref21">21</xref>], the significant increase of A also accelerate the reaction, hence the photo-degradation efficiency of MO is much higher than other Cu<sub>2</sub>O samples [<xref ref-type="bibr" rid="scirp.67486-ref13">13</xref>]-[<xref ref-type="bibr" rid="scirp.67486-ref16">16</xref>].</p></sec><sec id="s3_4"><title>3.4. Photo-Catalytic Efficiency of Seven Times Recycling Use of Catalyst</title><p>Stability of Cu<sub>2</sub>O was investigated by reuse 7 times shows in <xref ref-type="fig" rid="fig5">Figure 5</xref> It indicates that the efficiency change from 95.84% to 76.1%. The X-ray patterns of residual Cu<sub>2</sub>O after the seventh recycled, as shown in <xref ref-type="fig" rid="fig6">Figure 6</xref>(b), is same as before use. So, the sea urchin-like Cu<sub>2</sub>O prepared is much stable in the photo-catalysis process under the acidic conditions.</p></sec></sec><sec id="s4"><title>4. Conclusion</title><p>The sea urchin-like Cu<sub>2</sub>O has highly active to degradation of MO under visible light irradiation. Degradation rate was achieved to 94.37% within 25 min. The photo degradation of MO follows the Langmuir-Hinshelwood model and belonging to the first-order reaction. The activation energy and pre-exponential factor are 41.18 KJ∙mol<sup>−1</sup> and 1.07 &#215; 10<sup>6</sup>, respectively. After seven times recycling, the Cu<sub>2</sub>O still showed higher photo-catalytic</p><fig id="fig4"  position="float"><label><xref ref-type="fig" rid="fig4">Figure 4</xref></label><caption><title> Dependence of the first-order kinetics constant and temperature</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/67486x15.png"/></fig><fig id="fig5"  position="float"><label><xref ref-type="fig" rid="fig5">Figure 5</xref></label><caption><title> The degradation to MO of sea urchin-like Cu<sub>2</sub>O photo-catalyst at different reuse times</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/67486x16.png"/></fig><fig id="fig6"  position="float"><label><xref ref-type="fig" rid="fig6">Figure 6</xref></label><caption><title> XRD patterns of sea urchin like (a) before use (b) after reuse for seven times</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/67486x17.png"/></fig><p>efficiency and stability.</p></sec><sec id="s5"><title>Cite this paper</title><p>R. J. Gao,T. Ding,X. J. Duan, (2016) Kinetics Study on Photocatalytic Degradation of Methyl Orange Catalyzed by Sea Urchin-Like Cu2O. Journal of Materials Science and Chemical Engineering,04,35-40. doi: 10.4236/msce.2016.46005</p></sec></body><back><ref-list><title>References</title><ref id="scirp.67486-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Kim, J.Y., Rodriguez, J.A. and Hanson, J.C. (2003) Reduction of CuO and Cu2O with H2:H Embedding and Kinetic Effectsinthe Formation of Suboxides. The Journal American Chemical Society, 125, 10684-10692.  
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