<?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">JMP</journal-id><journal-title-group><journal-title>Journal of Modern Physics</journal-title></journal-title-group><issn pub-type="epub">2153-1196</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/jmp.2018.913149</article-id><article-id pub-id-type="publisher-id">JMP-88767</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Physics&amp;Mathematics</subject></subj-group></article-categories><title-group><article-title>
 
 
  Empirical Relation of the Fine-Structure Constant with the Transference Number Concept
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Tomofumi</surname><given-names>Miyashita</given-names></name><xref ref-type="aff" rid="aff1"><sub>1</sub></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib></contrib-group><aff id="aff1"><label>1</label><addr-line>Miyashita Clinic, Huruno-cho, Kawachinagano, Osaka, Japan</addr-line></aff><pub-date pub-type="epub"><day>01</day><month>11</month><year>2018</year></pub-date><volume>09</volume><issue>13</issue><fpage>2346</fpage><lpage>2353</lpage><history><date date-type="received"><day>22,</day>	<month>October</month>	<year>2018</year></date><date date-type="rev-recd"><day>24,</day>	<month>November</month>	<year>2018</year>	</date><date date-type="accepted"><day>27,</day>	<month>November</month>	<year>2018</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>
 
 
  The fine-structure constant of 1/137 is puzzling and has never been fully explained. When the interaction coefficient is 1/137, the transference number should be 136/137. With the transference number concept, we noticed that we must examine the constant of 1/136 instead of 1/137 to discover an empirical relationship in which the fine-structure constant is related to the mass ratio of electrons and quarks. Then, the physical meaning of this empirical relationship is discussed.
 
</p></abstract><kwd-group><kwd>Wagner’s Equation</kwd><kwd> Fluctuation and Dissipation Theory</kwd><kwd> Boltzmann Distribution</kwd><kwd> Maxwell’s Demon</kwd><kwd> Additional Thermodynamic Law</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Previously, we tried to explain quantum physics using classical thermodynamics [<xref ref-type="bibr" rid="scirp.88767-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.88767-ref2">2</xref>] . However, these discussions were lacking evidential support, prompting us to search for this evidence.</p><p>Solid-oxide fuel cells (SOFCs) directly convert the chemical energy of fuel gases, such as hydrogen and methane, into electrical energy. SOFCs use a solid-oxide film as the electrolyte, and oxygen ions serve as the main charge carriers. Typically, yttria-stabilized zirconia (YSZ) is used as the electrolyte material in these cells. The open-circuit voltage (OCV) of the YSZ electrolyte is equal to the Nernst voltage (V<sub>th</sub>) of 1.15 V at 1073 K. However, using samaria-doped ceria (SDC) electrolytes, the OCV is approximately 0.8 V. The low OCV was calculated using Wagner’s equation, which is based on the chemical equilibrium theory. Wagner’s equation [<xref ref-type="bibr" rid="scirp.88767-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.88767-ref4">4</xref>] is</p><p>J O 2 = − R T 16 F 2 L ∫ ln p O 2 a n o d e ln p O 2 c a t h o d e σ e l σ i o n σ e l + σ i o n d ln p O 2 (1)</p><p>where J O 2 and pO<sub>2</sub> are the O<sub>2</sub> flux and the O<sub>2</sub> partial pressure, respectively; p O 2 c a t h o d e and p O 2 a n o d e are the O<sub>2</sub> partial pressures at the cathode and anode, respectively; R, T, and F are the gas constant, the absolute temperature, and Faraday’s constant, respectively; L is the thickness of the membrane or film; and σ<sub>el</sub> and σ<sub>ion</sub> are the conductivities of the electrons and oxygen vacancies, respectively.</p><p>From Equations (1), Equations (2) and (3) can be deduced [<xref ref-type="bibr" rid="scirp.88767-ref5">5</xref>] :</p><p>O C V = V t h − R i I i (2)</p><p>where R<sub>i</sub> and I<sub>i</sub> are the ionic resistances of the electrolyte and the ionic current, respectively.</p><p>O C V = R T 4 F ∫ ln p O 2 a n o d e ln p O 2 c a t h o d e t i o n d ln p O 2 (3)</p><p>Parameter t<sub>ion</sub> is expressed as</p><p>t i o n = σ i o n σ e l + σ i o n (4)</p><p>However, s<sub>el</sub> is a function of the O<sub>2</sub> partial pressure [<xref ref-type="bibr" rid="scirp.88767-ref6">6</xref>] :</p><p>σ e l = σ i o n ( p O 2 p O 2 ∗ ) − 1 4 (5)</p><p>where p O 2 ∗ corresponds to the oxygen partial pressure at which t<sub>ion</sub> = 1/2. When t<sub>ion</sub> is constant in the electrolytes,</p><p>O C V = t i o n &#215; V t h (6)</p><p>The low OCV was thought to be due to the low value of the ionic transference number (t<sub>ion</sub>). However, experimentally, I<sub>i</sub> in Equation (2) is negligible [<xref ref-type="bibr" rid="scirp.88767-ref6">6</xref>] [<xref ref-type="bibr" rid="scirp.88767-ref7">7</xref>] [<xref ref-type="bibr" rid="scirp.88767-ref8">8</xref>] [<xref ref-type="bibr" rid="scirp.88767-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.88767-ref10">10</xref>] . Considering the direction of the electrical field, there are serious problems in Wagner’s equation [<xref ref-type="bibr" rid="scirp.88767-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.88767-ref10">10</xref>] . Therefore, the voltage loss should be explained by other reasons.</p><p>Over the past two decades, the understanding of nonequilibrium thermodynamics has been enhanced by fluctuation and dissipation theorems such as the Jarzynski and Crooks relations [<xref ref-type="bibr" rid="scirp.88767-ref11">11</xref>] [<xref ref-type="bibr" rid="scirp.88767-ref12">12</xref>] . The autonomous Maxwell’s demon concept was proposed by Jarzynski [<xref ref-type="bibr" rid="scirp.88767-ref13">13</xref>] , and we independently discovered the equation for this concept [<xref ref-type="bibr" rid="scirp.88767-ref14">14</xref>] . In our equation, t<sub>ion</sub> remains important. In addition, we determined the empirical relationship and discussed the physical meaning of this empirical relationship.</p></sec><sec id="s2"><title>2. Equation for Autonomous Maxwell’s Demons</title><sec id="s2_1"><title>2.1. Main Problems in Wagner’s Equation</title><p>According to Michael Faraday, the direction of the electrical field is from the anode to the cathode. In the 1950s, Wagner studied mixed conductors with positively and negatively charged ions. However, Wagner’s equation was used for doped ceria electrolytes in which there are two negative carriers (oxygen ions and electrons). The ionic current (I<sub>i</sub>) and electron drift current (I<sub>e_drift</sub>) flow from the cathode to the anode. Only the electron diffusion current (I<sub>e_diffusion</sub>) can flow from the anode to the cathode. A schematic drawing of the directions of I<sub>i</sub>, I<sub>e_drift</sub> and I<sub>e_diffusion</sub> is presented in <xref ref-type="fig" rid="fig1">Figure 1</xref>. According to Weppner [<xref ref-type="bibr" rid="scirp.88767-ref15">15</xref>] , there should be a delay for I<sub>e_diffusion</sub>:</p><p>τ = L 2 D ˜ (7)</p><p>where τ, L, and D ˜ are the equilibrium time, sample length, and chemical diffusion coefficient, respectively. According to Wang [<xref ref-type="bibr" rid="scirp.88767-ref16">16</xref>] , D ˜ is 3.2 &#215; 10<sup>−6</sup> cm<sup>2</sup>/s at 1073 K. Therefore, using 1-mm-thick SDC electrolytes, τ should be 52 min at 1073 K. However, such a delay has been never observed during the transient process, so the existence of I<sub>e_diffusion</sub> can be disproved [<xref ref-type="bibr" rid="scirp.88767-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.88767-ref10">10</xref>] .</p></sec><sec id="s2_2"><title>2.2. Autonomous Maxwell’s Demons Explanation</title><p>We discovered the following empirical equation using SDC electrolytes [<xref ref-type="bibr" rid="scirp.88767-ref14">14</xref>] :</p><p>O C V = V t h − E a 2 e (8)</p><p>where e is elemental charge. E<sub>a</sub> is the ionic activation energy, which is 0.7 eV for SDC electrolytes. Therefore, the OCV in Equation (1) is 0.80 V (=1.15 V − 0.7 eV/2e). This equation is explained in Figures 2-4. The Boltzmann distribution of oxygen ions in the electrolyte at 1073 K is displayed in <xref ref-type="fig" rid="fig2">Figure 2</xref>. The ions with energies exceeding E<sub>a</sub> become carriers (hopping ions). <xref ref-type="fig" rid="fig3">Figure 3</xref> presents an incorrect carrier distribution. The Boltzmann distribution cannot be separated using passive filters because of the phenomenon known as “Maxwell’s demon”, and an accurate distribution is provided in <xref ref-type="fig" rid="fig4">Figure 4</xref>. The loss of Gibbs energy is illustrated in <xref ref-type="fig" rid="fig3">Figure 3</xref>. Equation (8) is correct, when t<sub>ion</sub> is zero. When t<sub>ion</sub> is not zero, the equation for autonomous Maxwell’s demon [<xref ref-type="bibr" rid="scirp.88767-ref14">14</xref>] [<xref ref-type="bibr" rid="scirp.88767-ref17">17</xref>] is</p><p>O C V = V t h − ( 1 − t i o n ) &#215; E a 2 e (9)</p></sec></sec><sec id="s3"><title>3. Empirical Relations of the Fine-Structure Constant with the Transference Number Concept</title><p>The fine-structure constant (α) is</p><p>α = e 2 4 π ε 0 ℏ c (10)</p><p>where π, ħ, c and ε<sub>0</sub> are the mathematical constant pi, the reduced Planck constant, the speed of light in a vacuum and the electric constant or permittivity of free space, respectively.</p><p>R K = h e 2 (11)</p><p>Here, R<sub>K</sub> is the von Klitzing constant.</p><p>Z 0 = 1 ε 0 c (12)</p><p>Here, Z<sub>0</sub> is the characteristic impedance. Therefore,</p><p>α = Z 0 2 R k (13)</p><p>When the interaction coefficient is 1/137, the transference number should be 136/137. The parameter t<sub>ion</sub> is expressed as</p><p>t i o n = σ i o n σ e l + σ i o n = R e l R e l + R i o n (14)</p><p>where R<sub>e</sub> and R<sub>ion</sub> are the resistance values for electrons and ions, respectively. Here, σ<sub>ion</sub> can be defined even when the ions are blocked to move. In Equation (13), we assumed that the main carriers are electrons that must move with two unknown carriers belonged to the environment. Then, the transference number unknown carriers is</p><p>t u n k n o w n = R e l 2 R e l 2 + R u n k n o w n = R e l 2 ( R e l 2 + R u n k n o w n ) (15)</p><p>where R<sub>unknown</sub> is the resistance of unknown particles belonged to the environment. Equation (15) is similar to Equation (13), and α<sup>-</sup><sup>1</sup> is 137.035. Therefore,</p><p>R e l 2 R u n k n o n = 136.035 (16)</p><p>Next, we consider the mobility (μ):</p><p>σ = n e μ (17)</p><p>where n is the number of carriers.</p><p>2 n e l = n u n k n o w n (18)</p><p>Here, n<sub>el</sub> and n<sub>unknown</sub> are the number of electrons and the number of unknown particles, respectively.</p><p>μ = e m * τ (19)</p><p>Here, m<sup>*</sup> is the carrier effective mass, and τ is the average scattering time. When τ is constant,</p><p>m u n k n o w n m e l = 136.035 (20)</p><p>where m<sub>el</sub> and m<sub>unknown</sub> are the mass of electrons and the mass of unknown particles, respectively, and m<sub>el</sub> is 0.511 MeV. Therefore, we must search for the mass with an energy value of 69.50 MeV (=0.511 &#215; 136). The rest mass of a negatively charged pion has an energy of 139.57 MeV. Then, consider the following equation:</p><p>m π − = 2 m q u a r k + m e l (21)</p><p>where m<sub>p</sub><sub>-</sub> and m<sub>quark</sub> are the mass of the negatively charged pion and the mass of quarks, respectively. From Equation (21), m<sub>quark</sub> is 69.53 MeV, which is similar to 69.50 MeV. Therefore, our empirical equation is</p><p>m q u a r k m e l = 1 α − 1 (22)</p></sec><sec id="s4"><title>4. Discussion</title><p>We proposed a model in which there should be one free electron and two quarks belonged to the environment. Electrons receive the 1/137 energy of photons in the presence of an electrical field. Two quarks receive the 136/137 energy of photons. However, movement of the two quarks with the usual energy is blocked for unknown reasons. Thus, the 136/137 energy of photons should diffuse to the environment, meaning that the transference number of the space for electrons is 136/137, instead of 1, in the presence of an electrical field. We proposed that the quantity of 257,934 ohms (from the calculation of 258,123 − (377/2)) should be measured.</p><p>When two quarks can move with higher energy, the interaction coefficient of quarks should be 136/137 and the transference number of quarks should be 1/137. This is the explanation for the strong interaction. The diffusion response time of the mixed electronic and quark conductors depend exponentially on the distance. So, Yukawa potential can be explained.</p></sec><sec id="s5"><title>5. Conclusion</title><p>Using the transference number concept, we proposed an empirical relationship in which the fine-structure constant is related to the mass ratio of electrons and quarks. This empirical equation is determined to be correct with a 99.96% (69.50/69.53) accuracy. Furthermore, we proposed that the quantity of 257,934 ohms should be measured.</p></sec><sec id="s6"><title>Conflicts of Interest</title><p>The author declares no conflicts of interest regarding the publication of this paper.</p></sec><sec id="s7"><title>Cite this paper</title><p>Miyashita, T. (2018) Empirical Relation of the Fine-Structure Constant with the Transference Number Concept. Journal of Modern Physics, 9, 2346-2353. https://doi.org/10.4236/jmp.2018.913149</p></sec></body><back><ref-list><title>References</title><ref id="scirp.88767-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Miyashita, T. (2011) Quantum Physics Can Be Understood in Terms of Classical Thermodynamics. Journal of Modern Physics, 2, 26-29. https://doi.org/10.4236/jmp.2011.21005</mixed-citation></ref><ref id="scirp.88767-ref2"><label>2</label><mixed-citation publication-type="other" xlink:type="simple">Miyashita, T. (2017) Bell’s Non-Locality Theorem Can Be Understood in Terms of Classical Thermodynamics. Journal of Modern Physics, 8, 87-98. https://doi.org/10.4236/jmp.2017.81008</mixed-citation></ref><ref id="scirp.88767-ref3"><label>3</label><mixed-citation publication-type="other" xlink:type="simple">Wagner, C. (1975) Equations for Transport in Solid Oxides and Sulfides of Transition Metals. Progress in Solid State Chemistry, 10, 3-16. https://doi.org/10.1016/0079-6786(75)90002-3</mixed-citation></ref><ref id="scirp.88767-ref4"><label>4</label><mixed-citation publication-type="book" xlink:type="simple">Bouwmeester, H.J.M. and Burggraaf, A.J. (1997) Dense Ceramic Membranes for Oxygen Separator. In: Gellings, P.J. and Bouwmeester, H.J.M., Eds., The CRC Handbook of Solid State Electrochemistry, CRC Press, New York, 481-553.</mixed-citation></ref><ref id="scirp.88767-ref5"><label>5</label><mixed-citation publication-type="other" xlink:type="simple">Miyashita, T. (2017) Equilibration Process in Response to a Change in Anode Gas Using Thick Sm-Doped Ceria Electrolytes in Solid-Oxide Fuel Cells. Journal of Electrochemical Society, 164, E3190-E3199 E. https://doi.org/10.1149/2.0251711jes</mixed-citation></ref><ref id="scirp.88767-ref6"><label>6</label><mixed-citation publication-type="book" xlink:type="simple">Kudo, T. (1997) Survey of Types of Solid Electrolytes. In: Gellings, P.J. and Bouwmeester, H.J.M., Eds., The CRC Handbook of Solid State Electrochemistry, CRC Press, New York, 195-221. https://doi.org/10.1201/9781420049305.ch6</mixed-citation></ref><ref id="scirp.88767-ref7"><label>7</label><mixed-citation publication-type="other" xlink:type="simple">Miyashita, T. (2006) Necessity of Verification of Leakage Currents Using Sm Doped Ceria Electrolytes in SOFCs. Journal of Materials Science, 41, 3183-3184. https://doi.org/10.1007/s10853-006-6371-8</mixed-citation></ref><ref id="scirp.88767-ref8"><label>8</label><mixed-citation publication-type="other" xlink:type="simple">Miyashita, T. (2011) Unchanged OCV Requires Concepts Considering Electrode Degradation Using Sm-Doped Ceria Electrolytes in SOFCs. Electrochemical and Solid-State Letters, 14, 1-4. https://doi.org/10.1149/1.3581208</mixed-citation></ref><ref id="scirp.88767-ref9"><label>9</label><mixed-citation publication-type="other" xlink:type="simple">Miyashita, T. (2014) A Current-Independent Constant Anode Voltage Loss Using Sm-Doped Ceria Electrolytes in SOFCs. ECS Transactions, 59, 53-61. https://doi.org/10.1149/05901.0053ecst</mixed-citation></ref><ref id="scirp.88767-ref10"><label>10</label><mixed-citation publication-type="other" xlink:type="simple">Miyashita, T. (2017) Current-Voltage Relationship Considering the Direction of the Electrical Field in Mixed Ionic-Electronic Solid Conductors. ECS Transactions, 80, 1057-1072. https://doi.org/10.1149/08010.1057ecst</mixed-citation></ref><ref id="scirp.88767-ref11"><label>11</label><mixed-citation publication-type="other" xlink:type="simple">Jarzynski, C. (1997) Nonequilibrium Equality for Free Energy Differences. Physical Review Letters, 78, 2690-2693. https://doi.org/10.1103/PhysRevLett.78.2690  arXiv: cond-mat/9610209</mixed-citation></ref><ref id="scirp.88767-ref12"><label>12</label><mixed-citation publication-type="other" xlink:type="simple">Crooks, G.E. (1999) Entropy Production Fluctuation Theorem and the Nonequilibrium Work Relation for Free Energy Differences. Physical Review E, 60, 2721-2726. https://doi.org/10.1103/PhysRevE.60.2721  arXiv:cond-mat/9901352</mixed-citation></ref><ref id="scirp.88767-ref13"><label>13</label><mixed-citation publication-type="other" xlink:type="simple">Jarzynski, C. (2012) Work and Information Processing in a Solvable Model of Maxwell’s Demon. Proceedings of National Academy of Sciences of the United States of America, 109, 11641-11645. https://doi.org/10.1073/pnas.1204263109</mixed-citation></ref><ref id="scirp.88767-ref14"><label>14</label><mixed-citation publication-type="other" xlink:type="simple">Miyashita, T. (2005) Empirical Equation about Open Circuit Voltage in SOFC. Journal of Materials Science, 40, 6027. https://doi.org/10.1007/s10853-005-4560-5</mixed-citation></ref><ref id="scirp.88767-ref15"><label>15</label><mixed-citation publication-type="other" xlink:type="simple">Thangadurai, V. and Weppner, W. (2004) Ce0.8Sm0.2O1.9: Characterization of Electronic Charge Carriers and Application in Limiting Current Oxygen Sensors. Electrochimica Acta, 49, 1577-1585. https://doi.org/10.1016/j.electacta.2003.11.019</mixed-citation></ref><ref id="scirp.88767-ref16"><label>16</label><mixed-citation publication-type="other" xlink:type="simple">Wang, S., Kobayashi, T., Dokiya, M. and Hashimoto, T. (2000) Electrical and Ionic Conductivity of Gd-Doped Ceria. Journal of Electrochemical Society, 147, 3606-3609. https://doi.org/10.1149/1.1393946</mixed-citation></ref><ref id="scirp.88767-ref17"><label>17</label><mixed-citation publication-type="other" xlink:type="simple">Miyashita, T. (2019) Open-Circuit Voltage Anomalies in Yttria-Stabilised Zirconia and Samaria Doped Ceria Bilayered Electrolytes. (To Be Published)</mixed-citation></ref></ref-list></back></article>