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<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">Front. Energy Res.</journal-id>
<journal-title>Frontiers in Energy Research</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Front. Energy Res.</abbrev-journal-title>
<issn pub-type="epub">2296-598X</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="publisher-id">667419</article-id>
<article-id pub-id-type="doi">10.3389/fenrg.2021.667419</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Energy Research</subject>
<subj-group>
<subject>Original Research</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>Coupled Modeling and Simulation of Phase Transformation in Zircaloy-4 Fuel Cladding Under Loss-of-Coolant Accident Conditions</article-title>
<alt-title alt-title-type="left-running-head">Lu et&#x20;al.</alt-title>
<alt-title alt-title-type="right-running-head">Phase Transformation in Zircaloy-4 Cladding</alt-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Lu</surname>
<given-names>Wenjun</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/1232358/overview"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Qian</surname>
<given-names>Libo</given-names>
</name>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/1074150/overview"/>
</contrib>
<contrib contrib-type="author" corresp="yes">
<name>
<surname>Zhou</surname>
<given-names>Wenzhong</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="aff" rid="aff3">
<sup>3</sup>
</xref>
<xref ref-type="corresp" rid="c001">&#x2a;</xref>
<uri xlink:href="https://loop.frontiersin.org/people/1066467/overview"/>
</contrib>
</contrib-group>
<aff id="aff1">
<label>
<sup>1</sup>
</label>Sino-French Institute of Nuclear Engineering and Technology, Sun Yat-Sen University, <addr-line>Zhuhai</addr-line>, <country>China</country>
</aff>
<aff id="aff2">
<label>
<sup>2</sup>
</label>Nuclear Power Institute of China, <addr-line>Chengdu</addr-line>, <country>China</country>
</aff>
<aff id="aff3">
<label>
<sup>3</sup>
</label>Department of Mechanical Engineering, City University of Hong Kong, <addr-line>Hong Kong</addr-line>, <country>China</country>
</aff>
<author-notes>
<fn fn-type="edited-by">
<p>
<bold>Edited by:</bold> <ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/759754/overview">Mingjun Wang</ext-link>, Xi&#x2019;an Jiaotong University, China</p>
</fn>
<fn fn-type="edited-by">
<p>
<bold>Reviewed by:</bold> <ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/1074785/overview">Juliana P. Duarte</ext-link>, Virginia Tech, United&#x20;States</p>
<p>
<ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/554619/overview">Luteng Zhang</ext-link>, Chongqing University, China</p>
</fn>
<corresp id="c001">&#x2a;Correspondence: Wenzhong Zhou, <email>zhouwzh3@mail.sysu.edu.cn</email>
</corresp>
<fn fn-type="other">
<p>This article was submitted to Nuclear Energy, a section of the journal Frontiers in Energy Research</p>
</fn>
</author-notes>
<pub-date pub-type="epub">
<day>09</day>
<month>06</month>
<year>2021</year>
</pub-date>
<pub-date pub-type="collection">
<year>2021</year>
</pub-date>
<volume>9</volume>
<elocation-id>667419</elocation-id>
<history>
<date date-type="received">
<day>13</day>
<month>02</month>
<year>2021</year>
</date>
<date date-type="accepted">
<day>26</day>
<month>05</month>
<year>2021</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#xa9; 2021 Lu, Qian and Zhou.</copyright-statement>
<copyright-year>2021</copyright-year>
<copyright-holder>Lu, Qian and Zhou</copyright-holder>
<license xlink:href="http://creativecommons.org/licenses/by/4.0/">
<p>This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these&#x20;terms.</p>
</license>
</permissions>
<abstract>
<p>Under loss-of-coolant conditions, the temperature on fuel cladding will increase rapidly (up to 1000&#x2013;1500&#xa0;K), which will not only cause a dramatic oxidation reaction of Zircaloy-4 and an increase in hydrogen concentration but also cause an allotropic phase transformation of Zircaloy-4 from hexagonal (&#x3b1;-pahse) to cubic (&#x3b2;-phase) crystal structure. As we all know, thermophysical properties have a close relationship with the microstructure of the material. Moreover, because of an important influence of the phase transformation on the creep resistance and the ductility of the fuel rod, studying the crystallographic phase transformation kinetics is pivotal for evaluating properties for fuel rod completeness. We coupled the phase transformation model together with the existing physical models for reactor fuel, gap, cladding, and coolant, based on the finite element analysis and simulation software COMSOL Multiphysics. The critical parameter for this transformation is the evolution of the volume fraction of the favored phase described by a function of time and temperature. Hence, we choose two different volume fractions (0 and 10%) of BeO for UO<sub>2</sub>-BeO enhanced thermal conductivity nuclear fuel and zircaloy cladding as objects of this study. In order to simulate loss-of-coolant accident conditions, five relevant parameters are studied, including the gap size between fuel and cladding, the temperature at the extremities of the fuel element, the coefficient of heat transfer, the linear power rate, and the coolant temperature, to see their influence on the behavior of phase transformation under non-isothermal conditions. The results show that the addition of 10vol%BeO in the UO<sub>2</sub> fuel decreased the phase transformation effect a lot, and no significant phase transformation was observed in Zircaloy-4 cladding with UO<sub>2</sub>-BeO enhanced thermal conductivity nuclear fuel during existing loss-of-coolant accident conditions.</p>
</abstract>
<kwd-group>
<kwd>phase transformation</kwd>
<kwd>zircaloy-4</kwd>
<kwd>LOCA</kwd>
<kwd>accident tolerant fuel (ATF)</kwd>
<kwd>fully coupled</kwd>
</kwd-group>
<contract-sponsor id="cn001">Nuclear Power Institute of China<named-content content-type="fundref-id">10.13039/100012842</named-content>
</contract-sponsor>
<contract-sponsor id="cn002">Fundamental Research Funds for the Central Universities<named-content content-type="fundref-id">10.13039/501100012226</named-content>
</contract-sponsor>
<contract-sponsor id="cn003">International Science and Technology Cooperation Programme<named-content content-type="fundref-id">10.13039/501100012326</named-content>
</contract-sponsor>
<contract-sponsor id="cn004">Major Projects of Guangdong Education Department for Foundation Research and Applied Research<named-content content-type="fundref-id">10.13039/501100012576</named-content>
</contract-sponsor>
</article-meta>
</front>
<body>
<sec id="s1">
<title>Introduction</title>
<p>With the increasing energy demand, human beings have never stopped exploring new energy sources. Among them, nuclear energy is one of the most popular and promising future energy sources. Although nuclear energy is considered a clean and efficient energy source, it deals with a serious hazard - nuclear radiation. Many studies have shown that complex lesions can easily occur in cellular DNA (<xref ref-type="bibr" rid="B29">Sutherland et&#x20;al., 2000</xref>; <xref ref-type="bibr" rid="B30">Sutherland et&#x20;al., 2001</xref>; <xref ref-type="bibr" rid="B33">Yang et&#x20;al., 2004</xref>), which means that nuclear radiation can cause massive damage to the human body, causing people to suffer from cancer and even&#x20;death.</p>
<p>Nearly 70&#xb0;years have passed, nuclear energy has been developed from the 1950s to the present. In these years, nuclear energy&#x2019;s development process is not smooth sailing, which means that there have been accidents in nuclear energy development history. Some major nuclear power cases have attracted the whole world&#x2019;s attention on nuclear safety, such as the Chernobyl nuclear leak accident in 1986, rated as INES 7 and considered the worst nuclear power accident in history. More recently, the Fukushima Daiichi Nuclear Power Plant accident in 2011, which is also rated as INES 7, brought widespread attention. These accidents caused substantial economic losses and caused many people to be exposed to varying degrees of radiation pollution, affecting health and even losing their lives. What is more, huge adverse effects have been caused on nuclear energy development worldwide. Thus, safety issues occupy a vital position in the development of nuclear energy.</p>
<p>With respect that an entire reactor of a nuclear power station is incredibly complex, there are many ways to ensure nuclear power plants&#x2019; safety. One of the critical aspects is how to avert the leakage of radioactive energy as much as possible in a loss-of-coolant accident (LOCA). In LOCA, the pivotal step to controlling nuclear leakage is to maintain the nuclear fuel rod&#x2019;s integrity and the fuel cladding when they are inserted into cold water under the emergency cooling system. If the fuel cladding is not firm and tenacious enough, the nuclear fuel rod may crack easily, causing the radioactive material to break through the cladding and leak, resulting in severe consequences. Subsequently, accident tolerant fuel and cladding materials under LOCA conditions are studied by many researchers (<xref ref-type="bibr" rid="B31">Isobe and Suda, 1999</xref>; <xref ref-type="bibr" rid="B7">Forgeron et&#x20;al., 2000a</xref>; <xref ref-type="bibr" rid="B19">Manng&#xe5;rd et&#x20;al., 2011</xref>; <xref ref-type="bibr" rid="B18">Manng&#xe5;rd and Massih, 2011</xref>; <xref ref-type="bibr" rid="B26">Sawarn et&#x20;al., 2014</xref>; <xref ref-type="bibr" rid="B25">Park et&#x20;al., 2016</xref>; <xref ref-type="bibr" rid="B28">Suman et&#x20;al., 2016</xref>; <xref ref-type="bibr" rid="B9">Gamble et&#x20;al., 2017</xref>; <xref ref-type="bibr" rid="B32">Tang et&#x20;al., 2017</xref>; <xref ref-type="bibr" rid="B13">Jailin et&#x20;al., 2020</xref>), especially after the event at Fukushima Daiichi Nuclear Power Plant.</p>
<p>Accident Tolerant Fuel, or ATF for short, is a new generation of the fuel system to improve the fuel element&#x2019;s ability to fight against severe accidents. Compared to the previous fuel system, this updated fuel system can resist grave accident conditions for a longer time and, in the meanwhile, maintain the same or have even better performance under normal operating conditions. The unique material characteristics of accident tolerant fuel can slow down the velocity of deterioration in severe cases, which would help people reclaim more valuable time to take emergency measures so that the radiation leakage risk of fuel is significantly reduced. To sum up, the critical point of accident tolerant fuel is the endurance capacity in a loss-of-coolant accident. For the moment, there are two effective methods to enhance this capacity, one is to find new material (such as SiC, FeCrAl) to replace the fuel cladding that we are using now, and the other is to enhance the properties of the existing fuel system (such as coating cladding, modifying fuel). For the former, the database of new cladding material on the physical properties and phenomena is scarce. There are still many properties and phenomena of existing cladding that are not well understood at present. Further research on the existing cladding material is beneficial to analyzing accident tolerant fuel and cladding as the object for comparison and validation (to keep its strong points and overcome the shortcomings). Our work has used UO<sub>2</sub>-BeO enhanced thermal conductivity nuclear fuel and zircaloy cladding as an accident tolerant fuel system, which means we have chosen the latter method to research the physical properties of cladding.</p>
<p>In today&#x2019;s nuclear energy industry, zirconium alloys (especially Zircaloy-4) are still widely used as structural materials for reactors due to their superior properties. The small thermal neutron capture cross-section of zirconium allows it to ensure sufficient thermal neutrons to sustain the reactor&#x2019;s normal operation. Also, zirconium alloy has the advantages of strong corrosion resistance (<xref ref-type="bibr" rid="B31">Isobe and Suda, 1999</xref>) and excellent mechanical properties, making the research of zirconium alloys internationally occupy an increasingly important position.</p>
<p>Under extreme conditions, such as in a loss-of-coolant accident, the fuel cladding will undergo a rapid temperature increase (up to 1000&#x2013;1500&#xa0;K) (<xref ref-type="bibr" rid="B11">Hales et&#x20;al., 2016</xref>), which will not only cause a dramatic oxidation reaction of Zircaloy-4 and an increase in hydrogen concentration but also cause an allotropic phase transformation of Zircaloy-4 from hexagonal (&#x3b1;-pahse) to cubic (&#x3b2;-phase) crystal structure (<xref ref-type="bibr" rid="B24">Northwood and Lim, 1979</xref>). Thermophysical properties are closely related to the microstructure of the materials themselves. In other words, under LOCA conditions, the behavior of fuel rod cladding depends mainly on the metallurgical evolution at high temperatures. Researchers have also pointed out an important influence of the phase transformation on the creep resistance and ductility, two essential characteristics for fuel rod integrity (<xref ref-type="bibr" rid="B7">Forgeron et&#x20;al., 2000a</xref>). Therefore, studying the crystallographic phase transformation kinetics is pivotal for evaluating the mechanical properties essential for fuel rod completeness (deformation and burst) to improve its performance during LOCA conditions.</p>
<p>The essential parameter for the transformation kinetics is the evolution of the new phase&#x2019;s volume fraction as a function of time and temperature. This paper has selected the method for calculating the volume fraction of the advantageous phase in Zircaloy-4 as a function of time and temperature during phase transformation under non-isothermal conditions (<xref ref-type="bibr" rid="B11">Hales et&#x20;al., 2016</xref>).</p>
<p>This study has implemented the physical model of phase transformation coupled with the existing physical models for reactor fuel, gap, cladding, and coolant, based on the finite element analysis and simulation software COMSOL Multiphysics. COMSOL Multiphysics originated from the Toolbox of MATLAB, is a finite element analysis and simulation software that is good at coupling multiple physical fields described by the PDEs. Besides, some physical models of the UO<sub>2</sub>-BeO-Zircaloy fuel-cladding system have already been implemented (<xref ref-type="bibr" rid="B17">Liu et&#x20;al., 2015</xref>) into the COMSOL Multiphysics finite-element platform.</p>
</sec>
<sec id="s2">
<title>Implementation of Models</title>
<sec id="s2-1">
<title>Model Geometry</title>
<p>The model used in this work adopted a 2D axisymmetric plane with UO<sub>2</sub>-BeO fuel rod and Zircaloy-4 cladding (see <xref ref-type="fig" rid="F1">Figure&#x20;1A</xref>). For the reason of the periodic boundary condition in the axial direction, a single pellet is chosen to represent all the pellets with a mapped mesh (<italic>see</italic> <xref ref-type="fig" rid="F1">Figure&#x20;1B</xref>) (<xref ref-type="bibr" rid="B17">Liu et&#x20;al., 2015</xref>).</p>
<fig id="F1" position="float">
<label>FIGURE 1</label>
<caption>
<p>
<bold>(A)</bold> Geometry of 2D-axisymmetric, <bold>(B)</bold> pellet geometry with mapped&#x20;mesh.</p>
</caption>
<graphic xlink:href="fenrg-09-667419-g001.tif"/>
</fig>
</sec>
<sec id="s2-2">
<title>Phase Transformation</title>
<sec id="s2-2-1">
<title>Transition Model</title>
<p>We choose a variable y as the volume fraction of the new transformed phase (&#x3b2;-phase) as a function of time t and temperature T. The value of y is in the range of 0&#x2013;1. Following the research of Leblond and Devaux (<xref ref-type="bibr" rid="B16">Leblond and Devaux, 1984</xref>), we considered that the value of y and the steady-state or equilibrium value <inline-formula id="inf1">
<mml:math id="m1">
<mml:mrow>
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<mml:mo>)</mml:mo>
</mml:mrow>
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</mml:math>
</inline-formula> has not much difference at a given temperature <italic>T</italic>. In this case, we write<disp-formula id="e1">
<mml:math id="m2">
<mml:mrow>
<mml:mtable>
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<mml:mo>)</mml:mo>
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<mml:mo>&#x2212;</mml:mo>
<mml:mi>y</mml:mi>
</mml:mrow>
<mml:mrow>
<mml:msub>
<mml:mi>&#x3c4;</mml:mi>
<mml:mi>c</mml:mi>
</mml:msub>
<mml:mrow>
<mml:mo>(</mml:mo>
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</mml:mrow>
</mml:mtd>
</mml:mtr>
</mml:mtable>
</mml:mrow>
</mml:math>
<label>(1)</label>
</disp-formula>where <inline-formula id="inf2">
<mml:math id="m3">
<mml:mrow>
<mml:msub>
<mml:mi>&#x3c4;</mml:mi>
<mml:mi>c</mml:mi>
</mml:msub>
</mml:mrow>
</mml:math>
</inline-formula> is the characteristic time of phase transition. We can see that <xref ref-type="disp-formula" rid="e1">Eq. (1)</xref> has two external functions <inline-formula id="inf3">
<mml:math id="m4">
<mml:mrow>
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<mml:mi>s</mml:mi>
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</inline-formula> and <inline-formula id="inf4">
<mml:math id="m5">
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<mml:msub>
<mml:mi>&#x3c4;</mml:mi>
<mml:mi>c</mml:mi>
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</inline-formula>, depending on temperature, with <inline-formula id="inf5">
<mml:math id="m6">
<mml:mrow>
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<mml:mi>y</mml:mi>
<mml:mi>s</mml:mi>
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<mml:mo>)</mml:mo>
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</inline-formula> being the volume fraction of phase newly formed at the temperature T after an infinitely long time and <inline-formula id="inf6">
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</inline-formula>. Both of these functions are temperature-dependent quantities and can be derived from the experimental data. Under non-isothermal conditions, the temperature <italic>T</italic> may change as a function of time, and therefore <xref ref-type="disp-formula" rid="e1">Eq. (1)</xref> needs to be solved numerically. By putting the rate parameter <inline-formula id="inf7">
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<label>(2)</label>
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</p>
<p>To calculate volume fraction y as a function of time and temperature, we need to specify the two function <inline-formula id="inf8">
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</inline-formula>, which appear in <xref ref-type="disp-formula" rid="e2">Eq. (2)</xref> Firstly, let us consider the former function <inline-formula id="inf10">
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</mml:mrow>
</mml:mrow>
</mml:math>
</inline-formula>. The steady-state volume fraction experimental data under phase transformation show that <inline-formula id="inf11">
<mml:math id="m13">
<mml:mrow>
<mml:msub>
<mml:mi>y</mml:mi>
<mml:mi>s</mml:mi>
</mml:msub>
<mml:mrow>
<mml:mo>(</mml:mo>
<mml:mi>T</mml:mi>
<mml:mo>)</mml:mo>
</mml:mrow>
</mml:mrow>
</mml:math>
</inline-formula> has an S-shaped or sigmoid form (<xref ref-type="bibr" rid="B22">Massih, 2009</xref>). Thus, the equilibrium volume fraction of &#x3b2;-phase is represented by a sigmoid function of temperature.<disp-formula id="e3">
<mml:math id="m14">
<mml:mrow>
<mml:mtable>
<mml:mtr>
<mml:mtd>
<mml:mrow>
<mml:msub>
<mml:mi>y</mml:mi>
<mml:mi>s</mml:mi>
</mml:msub>
<mml:mrow>
<mml:mo>(</mml:mo>
<mml:mi>T</mml:mi>
<mml:mo>)</mml:mo>
</mml:mrow>
<mml:mo>&#x3d;</mml:mo>
<mml:mfrac>
<mml:mn>1</mml:mn>
<mml:mn>2</mml:mn>
</mml:mfrac>
<mml:mrow>
<mml:mo>[</mml:mo>
<mml:mrow>
<mml:mn>1</mml:mn>
<mml:mo>&#x2b;</mml:mo>
<mml:mi>tanh</mml:mi>
<mml:mrow>
<mml:mo>(</mml:mo>
<mml:mrow>
<mml:mfrac>
<mml:mrow>
<mml:mi>T</mml:mi>
<mml:mo>&#x2212;</mml:mo>
<mml:msub>
<mml:mi>T</mml:mi>
<mml:mrow>
<mml:mi>c</mml:mi>
<mml:mi>e</mml:mi>
<mml:mi>n</mml:mi>
<mml:mi>t</mml:mi>
</mml:mrow>
</mml:msub>
</mml:mrow>
<mml:mrow>
<mml:msub>
<mml:mi>T</mml:mi>
<mml:mrow>
<mml:mi>s</mml:mi>
<mml:mi>p</mml:mi>
<mml:mi>a</mml:mi>
<mml:mi>n</mml:mi>
</mml:mrow>
</mml:msub>
</mml:mrow>
</mml:mfrac>
</mml:mrow>
<mml:mo>)</mml:mo>
</mml:mrow>
</mml:mrow>
<mml:mo>]</mml:mo>
</mml:mrow>
</mml:mrow>
</mml:mtd>
</mml:mtr>
</mml:mtable>
</mml:mrow>
</mml:math>
<label>(3)</label>
</disp-formula>where <inline-formula id="inf12">
<mml:math id="m15">
<mml:mrow>
<mml:msub>
<mml:mi>T</mml:mi>
<mml:mrow>
<mml:mi>c</mml:mi>
<mml:mi>e</mml:mi>
<mml:mi>n</mml:mi>
<mml:mi>t</mml:mi>
</mml:mrow>
</mml:msub>
</mml:mrow>
</mml:math>
</inline-formula> and <inline-formula id="inf13">
<mml:math id="m16">
<mml:mrow>
<mml:msub>
<mml:mi>T</mml:mi>
<mml:mrow>
<mml:mi>s</mml:mi>
<mml:mi>p</mml:mi>
<mml:mi>a</mml:mi>
<mml:mi>n</mml:mi>
</mml:mrow>
</mml:msub>
</mml:mrow>
</mml:math>
</inline-formula> are material-specific coefficients connected to the center and span of the mixed-phase region, respectively. These two parameters are determined by<disp-formula id="e4">
<mml:math id="m17">
<mml:mrow>
<mml:mtable>
<mml:mtr>
<mml:mtd>
<mml:mrow>
<mml:msub>
<mml:mi>T</mml:mi>
<mml:mrow>
<mml:mi>c</mml:mi>
<mml:mi>e</mml:mi>
<mml:mi>n</mml:mi>
<mml:mi>t</mml:mi>
</mml:mrow>
</mml:msub>
<mml:mo>&#x3d;</mml:mo>
<mml:mfrac>
<mml:mrow>
<mml:msub>
<mml:mi>T</mml:mi>
<mml:mi>&#x3b1;</mml:mi>
</mml:msub>
<mml:mo>&#x2b;</mml:mo>
<mml:msub>
<mml:mi>T</mml:mi>
<mml:mi>&#x3b2;</mml:mi>
</mml:msub>
</mml:mrow>
<mml:mn>2</mml:mn>
</mml:mfrac>
<mml:mo>;</mml:mo>
<mml:mo>&#xa0;</mml:mo>
<mml:msub>
<mml:mi>T</mml:mi>
<mml:mrow>
<mml:mi>s</mml:mi>
<mml:mi>p</mml:mi>
<mml:mi>a</mml:mi>
<mml:mi>n</mml:mi>
</mml:mrow>
</mml:msub>
<mml:mo>&#x3d;</mml:mo>
<mml:mfrac>
<mml:mrow>
<mml:msub>
<mml:mi>T</mml:mi>
<mml:mi>&#x3b2;</mml:mi>
</mml:msub>
<mml:mo>&#x2212;</mml:mo>
<mml:msub>
<mml:mi>T</mml:mi>
<mml:mrow>
<mml:mi>c</mml:mi>
<mml:mi>e</mml:mi>
<mml:mi>n</mml:mi>
<mml:mi>t</mml:mi>
</mml:mrow>
</mml:msub>
</mml:mrow>
<mml:mrow>
<mml:mn>2.3</mml:mn>
</mml:mrow>
</mml:mfrac>
</mml:mrow>
</mml:mtd>
</mml:mtr>
</mml:mtable>
</mml:mrow>
</mml:math>
<label>(4)</label>
</disp-formula>where <inline-formula id="inf14">
<mml:math id="m18">
<mml:mrow>
<mml:msub>
<mml:mi>T</mml:mi>
<mml:mi>&#x3b1;</mml:mi>
</mml:msub>
</mml:mrow>
</mml:math>
</inline-formula> and <inline-formula id="inf15">
<mml:math id="m19">
<mml:mrow>
<mml:msub>
<mml:mi>T</mml:mi>
<mml:mi>&#x3b2;</mml:mi>
</mml:msub>
</mml:mrow>
</mml:math>
</inline-formula> are measured phase boundary temperatures corresponding to 99% &#x3b1;-phase and 99% &#x3b2;-phase fractions, respectively. For Zircaloy-4, we used <inline-formula id="inf16">
<mml:math id="m20">
<mml:mrow>
<mml:msub>
<mml:mi>T</mml:mi>
<mml:mrow>
<mml:mi>c</mml:mi>
<mml:mi>e</mml:mi>
<mml:mi>n</mml:mi>
<mml:mi>t</mml:mi>
</mml:mrow>
</mml:msub>
<mml:mo>&#x3d;</mml:mo>
<mml:mn>1159</mml:mn>
<mml:mo>&#x2212;</mml:mo>
<mml:mn>0.096</mml:mn>
<mml:mi>w</mml:mi>
<mml:mrow>
<mml:mo>(</mml:mo>
<mml:mi>K</mml:mi>
<mml:mo>)</mml:mo>
</mml:mrow>
</mml:mrow>
</mml:math>
</inline-formula> and <inline-formula id="inf17">
<mml:math id="m21">
<mml:mrow>
<mml:msub>
<mml:mi>T</mml:mi>
<mml:mrow>
<mml:mi>s</mml:mi>
<mml:mi>p</mml:mi>
<mml:mi>a</mml:mi>
<mml:mi>n</mml:mi>
</mml:mrow>
</mml:msub>
<mml:mo>&#x3d;</mml:mo>
<mml:mn>44</mml:mn>
<mml:mo>&#x2b;</mml:mo>
<mml:mn>0.026</mml:mn>
<mml:mi>w</mml:mi>
<mml:mrow>
<mml:mo>(</mml:mo>
<mml:mi>K</mml:mi>
<mml:mo>)</mml:mo>
</mml:mrow>
</mml:mrow>
</mml:math>
</inline-formula> (<xref ref-type="bibr" rid="B22">Massih, 2009</xref>), where <inline-formula id="inf18">
<mml:math id="m22">
<mml:mi>w</mml:mi>
</mml:math>
</inline-formula> is the hydrogen concentration in the range of 0&#x2013;1,000 weight parts per million hydrogen (wppm). We have chosen 500wppm for the value of <inline-formula id="inf19">
<mml:math id="m23">
<mml:mi>w</mml:mi>
</mml:math>
</inline-formula> because of the imperfection of the hydride formation&#x20;model.</p>
<p>In addition to the steady-state volume fraction <inline-formula id="inf20">
<mml:math id="m24">
<mml:mrow>
<mml:msub>
<mml:mi>y</mml:mi>
<mml:mi>s</mml:mi>
</mml:msub>
<mml:mrow>
<mml:mo>(</mml:mo>
<mml:mi>T</mml:mi>
<mml:mo>)</mml:mo>
</mml:mrow>
</mml:mrow>
</mml:math>
</inline-formula>, we also need to express the rate parameter <inline-formula id="inf21">
<mml:math id="m25">
<mml:mrow>
<mml:mi>k</mml:mi>
<mml:mrow>
<mml:mo>(</mml:mo>
<mml:mi>T</mml:mi>
<mml:mo>)</mml:mo>
</mml:mrow>
</mml:mrow>
</mml:math>
</inline-formula>, which is the inverse of <inline-formula id="inf22">
<mml:math id="m26">
<mml:mrow>
<mml:msub>
<mml:mi>&#x3c4;</mml:mi>
<mml:mi>c</mml:mi>
</mml:msub>
<mml:mrow>
<mml:mo>(</mml:mo>
<mml:mi>T</mml:mi>
<mml:mo>)</mml:mo>
</mml:mrow>
</mml:mrow>
</mml:math>
</inline-formula>, in detail.<disp-formula id="e5">
<mml:math id="m27">
<mml:mrow>
<mml:mtable>
<mml:mtr>
<mml:mtd>
<mml:mrow>
<mml:mi>k</mml:mi>
<mml:mo>&#x3d;</mml:mo>
<mml:msub>
<mml:mi>k</mml:mi>
<mml:mn>0</mml:mn>
</mml:msub>
<mml:mi>e</mml:mi>
<mml:mi>x</mml:mi>
<mml:mi>p</mml:mi>
<mml:mrow>
<mml:mo>[</mml:mo>
<mml:mrow>
<mml:mo>&#x2212;</mml:mo>
<mml:mfrac>
<mml:mi>E</mml:mi>
<mml:mrow>
<mml:msub>
<mml:mi>k</mml:mi>
<mml:mi>b</mml:mi>
</mml:msub>
<mml:mi>T</mml:mi>
<mml:mrow>
<mml:mo>(</mml:mo>
<mml:mi>t</mml:mi>
<mml:mo>)</mml:mo>
</mml:mrow>
</mml:mrow>
</mml:mfrac>
</mml:mrow>
<mml:mo>]</mml:mo>
</mml:mrow>
<mml:mo>&#x2b;</mml:mo>
<mml:msub>
<mml:mi>k</mml:mi>
<mml:mi>m</mml:mi>
</mml:msub>
</mml:mrow>
</mml:mtd>
</mml:mtr>
</mml:mtable>
</mml:mrow>
</mml:math>
<label>(5)</label>
</disp-formula>
</p>
<p>From <xref ref-type="disp-formula" rid="e5">Eq. 5</xref> , we can see that the rate parameter <inline-formula id="inf23">
<mml:math id="m28">
<mml:mrow>
<mml:mo>&#xa0;</mml:mo>
<mml:mi>k</mml:mi>
<mml:mrow>
<mml:mo>(</mml:mo>
<mml:mi>T</mml:mi>
<mml:mo>)</mml:mo>
</mml:mrow>
</mml:mrow>
</mml:math>
</inline-formula> is highly dependent on temperature. Here, <inline-formula id="inf24">
<mml:math id="m29">
<mml:mrow>
<mml:msub>
<mml:mi>k</mml:mi>
<mml:mn>0</mml:mn>
</mml:msub>
</mml:mrow>
</mml:math>
</inline-formula> and <inline-formula id="inf25">
<mml:math id="m30">
<mml:mrow>
<mml:msub>
<mml:mi>k</mml:mi>
<mml:mi>b</mml:mi>
</mml:msub>
</mml:mrow>
</mml:math>
</inline-formula> are used to represent respectively the kinetic prefactor and the Boltzmann constant. E is used to show the total effective activation energy, and <inline-formula id="inf26">
<mml:math id="m31">
<mml:mrow>
<mml:msub>
<mml:mi>k</mml:mi>
<mml:mi>m</mml:mi>
</mml:msub>
</mml:mrow>
</mml:math>
</inline-formula> is just a constant changing with the direction of the phase transition. In this model, E is the effective activation energy, which associates the activation energy of nucleus formation and development. The justifiability of this associated effect has been discussed by Mittemeijer and his colleagues in (<xref ref-type="bibr" rid="B23">Mittemeijer, 1992</xref>; <xref ref-type="bibr" rid="B14">Kempen et&#x20;al., 2002</xref>). For Zircaloy-4, we use <inline-formula id="inf27">
<mml:math id="m32">
<mml:mrow>
<mml:msub>
<mml:mi>k</mml:mi>
<mml:mn>0</mml:mn>
</mml:msub>
<mml:mo>&#x3d;</mml:mo>
<mml:mn>60457</mml:mn>
<mml:mo>&#x2b;</mml:mo>
<mml:mn>18129</mml:mn>
<mml:mrow>
<mml:mo>&#x7c;</mml:mo>
<mml:mi>Q</mml:mi>
<mml:mo>&#x7c;</mml:mo>
</mml:mrow>
<mml:mrow>
<mml:mo>(</mml:mo>
<mml:mrow>
<mml:msup>
<mml:mi>S</mml:mi>
<mml:mrow>
<mml:mo>&#x2212;</mml:mo>
<mml:mn>1</mml:mn>
</mml:mrow>
</mml:msup>
</mml:mrow>
<mml:mo>)</mml:mo>
</mml:mrow>
</mml:mrow>
</mml:math>
</inline-formula> and <inline-formula id="inf28">
<mml:math id="m33">
<mml:mrow>
<mml:mi>E</mml:mi>
<mml:mo>/</mml:mo>
<mml:msub>
<mml:mi>k</mml:mi>
<mml:mi>b</mml:mi>
</mml:msub>
<mml:mo>&#xa0;</mml:mo>
<mml:mo>&#x3d;</mml:mo>
<mml:mn>16650</mml:mn>
<mml:mrow>
<mml:mo>(</mml:mo>
<mml:mi>K</mml:mi>
<mml:mo>)</mml:mo>
</mml:mrow>
</mml:mrow>
</mml:math>
</inline-formula> (<xref ref-type="bibr" rid="B22">Massih, 2009</xref>; <xref ref-type="bibr" rid="B19">Manng&#xe5;rd et&#x20;al., 2011</xref>), where <inline-formula id="inf29">
<mml:math id="m34">
<mml:mrow>
<mml:mi>Q</mml:mi>
<mml:mo>&#x3d;</mml:mo>
<mml:mi>d</mml:mi>
<mml:mi>T</mml:mi>
<mml:mo>/</mml:mo>
<mml:mi>d</mml:mi>
<mml:mi>t</mml:mi>
<mml:mrow>
<mml:mo>(</mml:mo>
<mml:mrow>
<mml:mi>K</mml:mi>
<mml:msup>
<mml:mi>s</mml:mi>
<mml:mrow>
<mml:mo>&#x2212;</mml:mo>
<mml:mn>1</mml:mn>
</mml:mrow>
</mml:msup>
</mml:mrow>
<mml:mo>)</mml:mo>
</mml:mrow>
</mml:mrow>
</mml:math>
</inline-formula> is used to represent the heat rate with <inline-formula id="inf30">
<mml:math id="m35">
<mml:mrow>
<mml:mrow>
<mml:mo>&#x7c;</mml:mo>
<mml:mi>Q</mml:mi>
<mml:mo>&#x7c;</mml:mo>
</mml:mrow>
<mml:mo>&#x2208;</mml:mo>
<mml:mrow>
<mml:mo>[</mml:mo>
<mml:mrow>
<mml:mn>0.1</mml:mn>
<mml:mo>,</mml:mo>
<mml:mn>100</mml:mn>
</mml:mrow>
<mml:mo>]</mml:mo>
</mml:mrow>
<mml:mo>&#xa0;</mml:mo>
<mml:mi>K</mml:mi>
<mml:msup>
<mml:mi>s</mml:mi>
<mml:mrow>
<mml:mo>&#x2212;</mml:mo>
<mml:mn>1</mml:mn>
</mml:mrow>
</mml:msup>
</mml:mrow>
</mml:math>
</inline-formula> (<xref ref-type="bibr" rid="B21">Massih and Jernkvist, 2009</xref>). The phase transformation <inline-formula id="inf31">
<mml:math id="m36">
<mml:mrow>
<mml:mi mathvariant="normal">&#x3b1;</mml:mi>
<mml:mo>&#x2192;</mml:mo>
<mml:mi mathvariant="normal">&#x3b2;</mml:mi>
</mml:mrow>
</mml:math>
</inline-formula> is entirely diffusion-controlled, while the transformation of the opposite direction is partly martensitic. This difference is revealed by the constant <inline-formula id="inf32">
<mml:math id="m37">
<mml:mrow>
<mml:msub>
<mml:mi>k</mml:mi>
<mml:mi>m</mml:mi>
</mml:msub>
</mml:mrow>
</mml:math>
</inline-formula> at the end of <xref ref-type="disp-formula" rid="e5">Eq. (5)</xref>, which is given in the form (<xref ref-type="bibr" rid="B19">Manng&#xe5;rd et&#x20;al., 2011</xref>)<disp-formula id="e6">
<mml:math id="m38">
<mml:mrow>
<mml:mtable>
<mml:mtr>
<mml:mtd>
<mml:mrow>
<mml:mrow>
<mml:mo>{</mml:mo>
<mml:mrow>
<mml:mtable>
<mml:mtr>
<mml:mtd>
<mml:mrow>
<mml:msub>
<mml:mi>k</mml:mi>
<mml:mi>m</mml:mi>
</mml:msub>
<mml:mo>&#x3d;</mml:mo>
<mml:mn>0</mml:mn>
<mml:mo>&#xa0;</mml:mo>
<mml:mo>&#xa0;</mml:mo>
<mml:mo>&#xa0;</mml:mo>
<mml:mo>&#xa0;</mml:mo>
<mml:mo>&#xa0;</mml:mo>
<mml:mo>&#xa0;</mml:mo>
<mml:mo>&#xa0;</mml:mo>
<mml:mo>&#xa0;</mml:mo>
<mml:mo>&#xa0;</mml:mo>
<mml:mi>&#x3b1;</mml:mi>
<mml:mo>&#x2192;</mml:mo>
<mml:mi>&#x3b2;</mml:mi>
</mml:mrow>
</mml:mtd>
</mml:mtr>
<mml:mtr>
<mml:mtd>
<mml:mrow>
<mml:msub>
<mml:mi>k</mml:mi>
<mml:mi>m</mml:mi>
</mml:msub>
<mml:mo>&#x3d;</mml:mo>
<mml:mn>0.2</mml:mn>
<mml:mo>&#xa0;</mml:mo>
<mml:mo>&#xa0;</mml:mo>
<mml:mo>&#xa0;</mml:mo>
<mml:mo>&#xa0;</mml:mo>
<mml:mo>&#xa0;</mml:mo>
<mml:mo>&#xa0;</mml:mo>
<mml:mi>&#x3b2;</mml:mi>
<mml:mo>&#x2192;</mml:mo>
<mml:mi>&#x3b1;</mml:mi>
</mml:mrow>
</mml:mtd>
</mml:mtr>
</mml:mtable>
</mml:mrow>
</mml:mrow>
</mml:mrow>
</mml:mtd>
</mml:mtr>
</mml:mtable>
</mml:mrow>
</mml:math>
<label>(6)</label>
</disp-formula>
</p>
</sec>
<sec id="s2-2-2">
<title>Threshold Temperature Models</title>
<p>For the material-dependent temperatures for the beginning of phase transformation, the experimental data on Zircaloy-4 show that this quantity depends on the heating or cooling rate <inline-formula id="inf33">
<mml:math id="m39">
<mml:mi>Q</mml:mi>
</mml:math>
</inline-formula> (<xref ref-type="bibr" rid="B8">Forgeron et&#x20;al., 2000b</xref>). In this model, we have used the relation below to calculate the starting temperature in Kelvin for <inline-formula id="inf34">
<mml:math id="m40">
<mml:mrow>
<mml:mi mathvariant="normal">&#x3b1;</mml:mi>
<mml:mo>&#x2192;</mml:mo>
<mml:mi mathvariant="normal">&#x3b1;</mml:mi>
<mml:mo>&#x2b;</mml:mo>
<mml:mi mathvariant="normal">&#x3b2;</mml:mi>
</mml:mrow>
</mml:math>
</inline-formula> transition based on the experimental data in (<xref ref-type="bibr" rid="B8">Forgeron et&#x20;al., 2000b</xref>; <xref ref-type="bibr" rid="B1">Brachet et&#x20;al., 2002</xref>).<disp-formula id="e7">
<mml:math id="m41">
<mml:mrow>
<mml:mtable>
<mml:mtr>
<mml:mtd>
<mml:mrow>
<mml:msub>
<mml:mi>T</mml:mi>
<mml:mrow>
<mml:mi mathvariant="bold">&#x3b1;</mml:mi>
<mml:mo>&#x2192;</mml:mo>
<mml:mi mathvariant="bold">&#x3b1;</mml:mi>
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<mml:mtable>
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<mml:mo>&#xa0;</mml:mo>
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<label>(7)</label>
</disp-formula>where <inline-formula id="inf35">
<mml:math id="m42">
<mml:mi>Q</mml:mi>
</mml:math>
</inline-formula> is the heating rate in Kelvin per second and the hydrogen concentration <inline-formula id="inf36">
<mml:math id="m43">
<mml:mi>w</mml:mi>
</mml:math>
</inline-formula> is in the range <inline-formula id="inf37">
<mml:math id="m44">
<mml:mrow>
<mml:mn>0</mml:mn>
<mml:mo>&#x2264;</mml:mo>
<mml:mi>w</mml:mi>
<mml:mo>&#x2264;</mml:mo>
<mml:mn>1000</mml:mn>
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</mml:math>
</inline-formula> wppm. Also, we have another relationship for the opposite direction of phase transformation basing on the experimental data of Zircaloy-4 reported in (<xref ref-type="bibr" rid="B8">Forgeron et&#x20;al., 2000b</xref>; <xref ref-type="bibr" rid="B1">Brachet et&#x20;al., 2002</xref>), i.e.,&#x20;from <inline-formula id="inf38">
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<mml:mrow>
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</inline-formula>.<disp-formula id="e8">
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<mml:mrow>
<mml:mtable>
<mml:mtr>
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<mml:mtext>&#x3b2;</mml:mtext>
<mml:mo>&#x2192;</mml:mo>
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<mml:mo>&#x3d;</mml:mo>
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<mml:mo>&#xa0;</mml:mo>
<mml:mo>&#xa0;</mml:mo>
<mml:mo>&#x2212;</mml:mo>
<mml:mn>0.1</mml:mn>
<mml:mo>&#x3c;</mml:mo>
<mml:mi>Q</mml:mi>
<mml:mo>&#x2264;</mml:mo>
<mml:mn>0</mml:mn>
<mml:mo>&#xa0;</mml:mo>
<mml:mi>K</mml:mi>
<mml:msup>
<mml:mi>s</mml:mi>
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<mml:mo>&#x2212;</mml:mo>
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<mml:mtd>
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<mml:msup>
<mml:mrow>
<mml:mrow>
<mml:mo>&#x7c;</mml:mo>
<mml:mi>Q</mml:mi>
<mml:mo>&#x7c;</mml:mo>
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</mml:mrow>
<mml:mrow>
<mml:mn>0.477</mml:mn>
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<mml:mo>&#xa0;</mml:mo>
<mml:mo>&#xa0;</mml:mo>
<mml:mo>&#xa0;</mml:mo>
<mml:mo>&#xa0;</mml:mo>
<mml:mo>&#xa0;</mml:mo>
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<mml:mn>100</mml:mn>
<mml:mo>&#x2264;</mml:mo>
<mml:mi>Q</mml:mi>
<mml:mo>&#x2264;</mml:mo>
<mml:mo>&#x2212;</mml:mo>
<mml:mn>0.1</mml:mn>
<mml:mo>&#xa0;</mml:mo>
<mml:mi>K</mml:mi>
<mml:msup>
<mml:mi>s</mml:mi>
<mml:mrow>
<mml:mo>&#x2212;</mml:mo>
<mml:mn>1</mml:mn>
</mml:mrow>
</mml:msup>
</mml:mrow>
</mml:mtd>
</mml:mtr>
</mml:mtable>
</mml:mrow>
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</mml:mrow>
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</mml:mtr>
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<label>(8)</label>
</disp-formula>
</p>
<p>A temperature (time) lag of the start temperature of phase transition from <inline-formula id="inf39">
<mml:math id="m47">
<mml:mi mathvariant="normal">&#x3b2;</mml:mi>
</mml:math>
</inline-formula> to <inline-formula id="inf40">
<mml:math id="m48">
<mml:mrow>
<mml:mi mathvariant="normal">&#x3b1;</mml:mi>
<mml:mo>&#x2b;</mml:mo>
<mml:mi mathvariant="normal">&#x3b2;</mml:mi>
</mml:mrow>
</mml:math>
</inline-formula> is observed in the cooling process. <xref ref-type="disp-formula" rid="e8">Eq. (8)</xref> is not symmetric with the equation on heating, i.e.,&#x20;<xref ref-type="disp-formula" rid="e7">Eq.&#x20;(7)</xref>.</p>
<p>All these material-dependent quantities above allow us to calculate the &#x3b2;-phase volume fraction as a function of time by numerical integration of <xref ref-type="disp-formula" rid="e2">Eq. (2)</xref>. Using the above-mentioned phase transformation models, the Zircaloy-4 cladding phase formation and redistribution can be investigated.</p>
</sec>
</sec>
</sec>
<sec id="s3">
<title>Modeling Results</title>
<p>The behavior of fuel and cladding are presented for a 2D axisymmetric LWR fuel rodlet in COMSOL Multiphysics. The 2D axisymmetric model simulates a simplified fuel pellet with a typical finite element mesh shown in <xref ref-type="fig" rid="F1">Figure&#x20;1B</xref>. The model contains an individual fuel pellet and Zircaloy-4 cladding. It is important to note a minimal but non-negligible gap between pellet and cladding considering the actual situation. A width of 80&#xb0;&#x3bc;m is considered to be the nominal gap size in this&#x20;model.</p>
<p>This section has used two different fuel systems, i.e.,&#x20;UO<sub>2</sub>-10% BeO and UO<sub>2</sub>, following the parameters setting in (<xref ref-type="bibr" rid="B17">Liu et&#x20;al., 2015</xref>). The UO2-BeO fuel properties are shown in <xref ref-type="sec" rid="s9">Supplementary Appendix S1</xref>. The typical RWR operating conditions used are shown in <xref ref-type="table" rid="T1">Table&#x20;1</xref>&#x20;above.</p>
<table-wrap id="T1" position="float">
<label>TABLE 1</label>
<caption>
<p>Input parameters for the axisymmetric problem under typical PWR operating conditions (<xref ref-type="bibr" rid="B17">Liu et&#x20;al., 2015</xref>).</p>
</caption>
<table>
<tbody valign="top">
<tr>
<td align="left">Linear average power (W/cm)</td>
<td align="center">200</td>
</tr>
<tr>
<td align="left">Fast neutron flux (n/m<sup>2</sup> s)</td>
<td align="center">9.5 &#xd7; 10<sup>17</sup>
</td>
</tr>
<tr>
<td align="left">Coolant pressure (MPa)</td>
<td align="center">15.5</td>
</tr>
<tr>
<td align="left">Coolant temperature (K)</td>
<td align="center">530</td>
</tr>
<tr>
<td align="left">Coolant convection coefficient (W/m<sup>2</sup> K)</td>
<td align="center">7,500</td>
</tr>
<tr>
<td align="left">Rod fill gas</td>
<td align="center">Helium</td>
</tr>
<tr>
<td align="left">Fill gas initial pressure (MPa)</td>
<td align="center">2.0</td>
</tr>
<tr>
<td align="left">Initial fuel density</td>
<td align="center">95% theoretical</td>
</tr>
</tbody>
</table>
</table-wrap>
<p>After implementing the phase transformation model for Zircaloy-4 cladding, we first calculated the volume fraction of &#x3b2;-phase under the normal operating condition to test this model, and we obtain <xref ref-type="fig" rid="F2">Figure&#x20;2</xref> as a result for the UO<sub>2</sub> fuel and Zircaloy-4 cladding.</p>
<fig id="F2" position="float">
<label>FIGURE 2</label>
<caption>
<p>Volume fraction of &#x3b2;-phase changing with temperature for UO<sub>2</sub> and Zircaloy-4 under normal operating conditions.</p>
</caption>
<graphic xlink:href="fenrg-09-667419-g002.tif"/>
</fig>
<p>
<xref ref-type="fig" rid="F2">Figure&#x20;2</xref> shows that the value of volume fraction of &#x3b2;-phase attains a very small magnitude. The green line with circles represents the volume fraction of &#x3b2;-phase of cladding outer-surface, while the blue line with asterisks represents the cladding inner-surface. Although the value of the inner surface of cladding is almost twice that of the outer surface, it is barely more than <inline-formula id="inf41">
<mml:math id="m49">
<mml:mrow>
<mml:mn>1.1</mml:mn>
<mml:mo>&#xd7;</mml:mo>
<mml:msup>
<mml:mrow>
<mml:mn>10</mml:mn>
</mml:mrow>
<mml:mrow>
<mml:mo>&#x2212;</mml:mo>
<mml:mn>7</mml:mn>
</mml:mrow>
</mml:msup>
</mml:mrow>
</mml:math>
</inline-formula> when it reaches its highest point, which means the effect of phase transformation in the Zircaloy-4 cladding is so small that it can be ignored under normal operating condition. The result calculated by this model is consistent with the figure shown in (<xref ref-type="bibr" rid="B11">Hales et&#x20;al., 2016</xref>). Then we estimated the effect of phase transformation under postulated loss-of-coolant accident conditions.</p>
<p>During a LOCA condition, on account of the decrease in heat-transfer capacity under loss-of-coolant accident conditions, the heat or energy generated in the fuel cannot be passed outside, which causes the changes in the boundary conditions between fuel elements. Hence it has a high possibility that the temperature at the extremities of the fuel element will rise higher than before. The boundary conditions will change between fuel elements and change between fuel, cladding, and coolant because heat transfer capability decreases. For example, the heat transfer coefficient between cladding and coolant will decrease in the transition boiling interval. If we consider the swelling effect of fission gas, the fuel diameter will grow a little, which will make the size of the gap between fuel and cladding smaller. The linear power rate will also rise from 20000&#xa0;W/m (set for normal condition) to 25,000&#xa0;W/m, even 30,000&#xa0;W/m when it is in serious condition. According to NRC (U.S. Nuclear Regulatory Commission) in (<xref ref-type="bibr" rid="B4">The U.S. Nuclear Regulatory Commission, 2011</xref>), a peak linear power density of around 60,000&#xa0;W/m is considered the safe limit for core in operation. Hence, we can also try to raise the linear power rate to 60,000&#xa0;W/m to observe its effect on phase transformation. The water saturation pressure at 530&#xa0;K is between 3.3469 and 4.6923&#xa0;MPa, according to Engineering Toolbox&#x2019;s data in (<xref ref-type="bibr" rid="B5">Engineering ToolBox (2004)</xref>. However, from <xref ref-type="fig" rid="F2">Figure&#x20;2</xref>, we can see the value of coolant pressure is up to 15.5&#xa0;MPa while the coolant temperature is only 530&#xa0;K. Per the data for water saturation pressure, the corresponding temperature of 15.5&#xa0;MPa is between 613 and 633&#xa0;K. In the following simulation, we have taken 613&#xa0;K as the coolant temperature into account during the calculations.</p>
<p>To simulate a relatively severe loss-of-coolant accident, we had reduced the physical size of the gap between fuel and cladding, raising the linear power generation rate, the coolant temperature, and the temperature at the extremities of the fuel element. For the sake of decreasing the heat transfer coefficient of cladding to coolant, we have multiplied the coefficient with a number less than one. All these conditions are taken into account simultaneously, and the results obtained are shown&#x20;below.</p>
<p>To make the results more clear, they are divided into four groups. The first group is the volume fraction of &#x3b2;-phase varying with the linear power rate, with 1500&#xa0;K - the temperature at the extremities of the fuel element, 8e&#x2212;7&#xa0;m - the gap size, and 0,6 - the coefficient multiplied with the heat transfer coefficient between cladding and coolant.</p>
<p>
<xref ref-type="fig" rid="F3">Figures 3A,C</xref> showed that the volume fraction on cladding inner-surface was increased almost by an order of magnitude from <inline-formula id="inf42">
<mml:math id="m50">
<mml:mrow>
<mml:mn>4.3</mml:mn>
<mml:mo>&#xd7;</mml:mo>
<mml:msup>
<mml:mrow>
<mml:mn>10</mml:mn>
</mml:mrow>
<mml:mrow>
<mml:mo>&#x2212;</mml:mo>
<mml:mn>5</mml:mn>
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</mml:mrow>
</mml:math>
</inline-formula> to <inline-formula id="inf43">
<mml:math id="m51">
<mml:mrow>
<mml:mn>2.6</mml:mn>
<mml:mo>&#xd7;</mml:mo>
<mml:msup>
<mml:mrow>
<mml:mn>10</mml:mn>
</mml:mrow>
<mml:mrow>
<mml:mo>&#x2212;</mml:mo>
<mml:mn>4</mml:mn>
</mml:mrow>
</mml:msup>
</mml:mrow>
</mml:math>
</inline-formula> when the linear power rate varied from 20,000&#x20;W/m to 25,000&#xa0;W/m. However, when the power rate is increased by an additional 5,000&#xa0;W/m to 30,000&#xa0;W/m in <xref ref-type="fig" rid="F3">Figure&#x20;3E</xref>, the volume fraction on the cladding inner-surface has reached 0.05, which is much bigger than before. Compared with UO<sub>2</sub>, the results for UO<sub>2</sub>-10vol%BeO in the left, i.e.,&#x20;<xref ref-type="fig" rid="F3">Figures 3B,D,F</xref>, are all smaller. The increment of linear power rate up to 30,000&#xa0;W/m for UO<sub>2</sub>-10vol%BeO did not have the same influence as that for UO<sub>2</sub> on the volume fraction of &#x3b2;-phase, which just attained around <inline-formula id="inf44">
<mml:math id="m52">
<mml:mrow>
<mml:mn>4.0</mml:mn>
<mml:mo>&#xd7;</mml:mo>
<mml:msup>
<mml:mrow>
<mml:mn>10</mml:mn>
</mml:mrow>
<mml:mrow>
<mml:mo>&#x2212;</mml:mo>
<mml:mn>4</mml:mn>
</mml:mrow>
</mml:msup>
</mml:mrow>
</mml:math>
</inline-formula> on the cladding inner-surface, the same magnitude for UO<sub>2</sub> with the linear power rate, which equals to 25,000&#xa0;W/m.</p>
<fig id="F3" position="float">
<label>FIGURE 3</label>
<caption>
<p>Volume fractions of &#x3b2;-phase on cladding inner surface and outer surface, changing with linear power rate, <bold>(A)</bold> 20,000&#xa0;W/m for UO<sub>2</sub> and Zircaloy-4, <bold>(B)</bold> 20,000&#xa0;W/m for UO<sub>2</sub>-10vol%BeO and Zircaloy-4, <bold>(C)</bold> 25,000&#xa0;W/m for UO<sub>2</sub> and Zircaloy-4, <bold>(D)</bold> 25,000&#xa0;W/m for UO<sub>2</sub>-10vol%BeO and Zircaloy-4, <bold>(E)</bold> 30,000&#xa0;W/m for UO<sub>2</sub> and Zircaloy-4, <bold>(F)</bold> 30,000&#xa0;W/m for UO<sub>2</sub>-10vol%BeO and Zircaloy-4.</p>
</caption>
<graphic xlink:href="fenrg-09-667419-g003.tif"/>
</fig>
<p>The second group is about the effect of the temperature at the extremities of fuel element on the volume fraction of &#x3b2;-phase, with 30,000&#xa0;W/m - the linear power rate, 8e&#x2212;7&#xa0;m- the gap size, and 0,6-the coefficient multiplied with the heat transfer coefficient between cladding and coolant.</p>
<p>
<xref ref-type="fig" rid="F4">Figure&#x20;4</xref> showed that there was not much difference in these results when the temperature at the extremities of the fuel element changed. From 700&#xa0;K to 1100&#xa0;K, the volume fractions on cladding inner-surface and outer-surface had all increased a little for both UO<sub>2</sub> and UO<sub>2</sub>-10vol%BeO, where the increments are nearly <inline-formula id="inf45">
<mml:math id="m53">
<mml:mrow>
<mml:mn>8</mml:mn>
<mml:mo>&#xd7;</mml:mo>
<mml:msup>
<mml:mrow>
<mml:mn>10</mml:mn>
</mml:mrow>
<mml:mrow>
<mml:mo>&#x2212;</mml:mo>
<mml:mn>3</mml:mn>
</mml:mrow>
</mml:msup>
</mml:mrow>
</mml:math>
</inline-formula> for UO<sub>2</sub> and <inline-formula id="inf46">
<mml:math id="m54">
<mml:mrow>
<mml:mn>2</mml:mn>
<mml:mo>&#xd7;</mml:mo>
<mml:msup>
<mml:mrow>
<mml:mn>10</mml:mn>
</mml:mrow>
<mml:mrow>
<mml:mo>&#x2212;</mml:mo>
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</inline-formula> for UO<sub>2</sub>-10vol%BeO on cladding inner surface. From 1100&#xa0;K to 1500&#xa0;K, the increment is noticeable for UO<sub>2</sub>-10vol%BeO compared with that from 700 to 1100&#xa0;K in <xref ref-type="fig" rid="F4">Figures 4B,D</xref>. We could see the volume fraction has increased around <inline-formula id="inf47">
<mml:math id="m55">
<mml:mrow>
<mml:mn>6</mml:mn>
<mml:mo>&#xd7;</mml:mo>
<mml:msup>
<mml:mrow>
<mml:mn>10</mml:mn>
</mml:mrow>
<mml:mrow>
<mml:mo>&#x2212;</mml:mo>
<mml:mn>5</mml:mn>
</mml:mrow>
</mml:msup>
</mml:mrow>
</mml:math>
</inline-formula> on the inner-surface for <xref ref-type="fig" rid="F4">Figures&#x20;4D,F</xref>.</p>
<fig id="F4" position="float">
<label>FIGURE 4</label>
<caption>
<p>Volume fractions of &#x3b2;-phase on cladding inner-surface and outer-surface, changing with the temperature at the extremities of the fuel element, <bold>(A)</bold> 700&#xa0;K for UO<sub>2</sub> and Zircaloy-4, <bold>(B)</bold> 700&#xa0;K for UO<sub>2</sub>-10vol%BeO and Zircaloy-4, <bold>(C)</bold> 1100&#xa0;K for UO<sub>2</sub> and Zircaloy-4, <bold>(D)</bold> 1100K for UO<sub>2</sub>-10vol%BeO and Zircaloy-4, <bold>(E)</bold> 1500&#xa0;K for UO<sub>2</sub> and Zircaloy-4, <bold>(F)</bold> 1500&#xa0;K for UO<sub>2</sub>-10vol%BeO and Zircaloy-4.</p>
</caption>
<graphic xlink:href="fenrg-09-667419-g004.tif"/>
</fig>
<p>The third group describes the variations of volume fraction of &#x3b2;-phase when the gap size changes. The other values are 0,6-the coefficient multiplied with the heat transfer coefficient between cladding and 30,000&#xa0;W/m - the linear power rate, 1500&#xa0;K-the temperature at the extremities of the fuel element.</p>
<p>In this group of calculations, we have selected three different magnitudes of gap size to observe the variations in the volume fraction of &#x3b2;-phase on cladding inner-surface and outer surface. We note that 8e&#x2212;5&#xa0;m in <xref ref-type="fig" rid="F5">Figures 5A,B</xref> is the initial gap size. From <xref ref-type="fig" rid="F5">Figures 5A,C</xref>, E, the gap size has increased tenfold and a 100 times, the volume fraction on cladding inner-surface has increased from 0.02 to 0.036 and from 0.02 to 0.052, respectively, while we nearly see no difference between <xref ref-type="fig" rid="F5">Figures 5B,D</xref>. In <xref ref-type="fig" rid="F5">Figures 5D,F</xref>, when the gap size had increased a hundred times, the volume fraction of &#x3b2;-phase on cladding inner-surface for UO<sub>2</sub>-10vol%BeO had increased a lot from <inline-formula id="inf48">
<mml:math id="m56">
<mml:mrow>
<mml:mn>2.8</mml:mn>
<mml:mo>&#xd7;</mml:mo>
<mml:msup>
<mml:mrow>
<mml:mn>10</mml:mn>
</mml:mrow>
<mml:mrow>
<mml:mo>&#x2212;</mml:mo>
<mml:mn>14</mml:mn>
</mml:mrow>
</mml:msup>
</mml:mrow>
</mml:math>
</inline-formula> to <inline-formula id="inf49">
<mml:math id="m57">
<mml:mrow>
<mml:mn>3.9</mml:mn>
<mml:mo>&#xd7;</mml:mo>
<mml:msup>
<mml:mrow>
<mml:mn>10</mml:mn>
</mml:mrow>
<mml:mrow>
<mml:mo>&#x2212;</mml:mo>
<mml:mn>4</mml:mn>
</mml:mrow>
</mml:msup>
</mml:mrow>
</mml:math>
</inline-formula>, which is much more apparent than the variation in <xref ref-type="fig" rid="F5">Figures 5B,D</xref>. Moreover, for UO<sub>2</sub>-10vol%BeO, the gap of volume fractions between two cladding surfaces has increased significantly from <xref ref-type="fig" rid="F5">Figures 5D&#x2013;F</xref>.</p>
<fig id="F5" position="float">
<label>FIGURE 5</label>
<caption>
<p>Volume fractions of &#x3b2;-phase on cladding inner-surface and outer-surface, changing with the gap size between the fuel and cladding, <bold>(A)</bold> 8e&#x2212;5&#xa0;m for UO<sub>2</sub> and Zircaloy-4, <bold>(B)</bold> 8e&#x2212;5&#xa0;m for UO<sub>2</sub>-10vol%BeO and Zircaloy-4, <bold>(C)</bold> 8e&#x2212;6&#xa0;m for UO<sub>2</sub> and Zircaloy-4, <bold>(D)</bold> 8e&#x2212;6&#xa0;m for UO<sub>2</sub>-10vol%BeO and Zircaloy-4, <bold>(E)</bold> 8e&#x2212;7&#xa0;m for UO<sub>2</sub> and Zircaloy-4, <bold>(F)</bold> 8e&#x2212;7&#xa0;m for UO<sub>2</sub>-10vol%BeO and Zircaloy-4.</p>
</caption>
<graphic xlink:href="fenrg-09-667419-g005.tif"/>
</fig>
<p>The last group is to observe the influence of the coefficient multiplied with the heat transfer coefficient between cladding and coolant on the volume fraction of &#x3b2;-phase, with 30,000&#xa0;W/m - the linear power rate, 1500&#xa0;K - the temperature at the extremities of the fuel element, and 8e&#x2212;7&#xa0;m- the gap&#x20;size.</p>
<p>In <xref ref-type="fig" rid="F6">Figures 6A,C,E</xref>, we can see the volume fractions of &#x3b2;-phase on both the cladding inner-surface and outer-surface for UO<sub>2</sub> increased rapidly when the heat transfer coefficient decreased. More specifically, when the coefficient decreased from 1 to 0.8, the volume fraction of &#x3b2;-phase for UO<sub>2</sub> on cladding inner-surface increased from <inline-formula id="inf50">
<mml:math id="m58">
<mml:mrow>
<mml:mn>3.5</mml:mn>
<mml:mo>&#xd7;</mml:mo>
<mml:msup>
<mml:mrow>
<mml:mn>10</mml:mn>
</mml:mrow>
<mml:mrow>
<mml:mo>&#x2212;</mml:mo>
<mml:mn>4</mml:mn>
</mml:mrow>
</mml:msup>
</mml:mrow>
</mml:math>
</inline-formula> to <inline-formula id="inf51">
<mml:math id="m59">
<mml:mrow>
<mml:mn>1.5</mml:mn>
<mml:mo>&#xd7;</mml:mo>
<mml:msup>
<mml:mrow>
<mml:mn>10</mml:mn>
</mml:mrow>
<mml:mrow>
<mml:mo>&#x2212;</mml:mo>
<mml:mn>3</mml:mn>
</mml:mrow>
</mml:msup>
</mml:mrow>
</mml:math>
</inline-formula>. When the coefficient decreased 0.2 again, i.e.,&#x20;from 0.8 to 0.6, the volume fraction of &#x3b2;-phase for UO<sub>2</sub> on cladding inner-surface increased from <inline-formula id="inf52">
<mml:math id="m60">
<mml:mrow>
<mml:mn>1.5</mml:mn>
<mml:mo>&#xd7;</mml:mo>
<mml:msup>
<mml:mrow>
<mml:mn>10</mml:mn>
</mml:mrow>
<mml:mrow>
<mml:mo>&#x2212;</mml:mo>
<mml:mn>3</mml:mn>
</mml:mrow>
</mml:msup>
</mml:mrow>
</mml:math>
</inline-formula> to <inline-formula id="inf53">
<mml:math id="m61">
<mml:mrow>
<mml:mn>5.2</mml:mn>
<mml:mo>&#xd7;</mml:mo>
<mml:msup>
<mml:mrow>
<mml:mn>10</mml:mn>
</mml:mrow>
<mml:mrow>
<mml:mo>&#x2212;</mml:mo>
<mml:mn>2</mml:mn>
</mml:mrow>
</mml:msup>
</mml:mrow>
</mml:math>
</inline-formula>. For <xref ref-type="fig" rid="F6">Figures 6B, D, F</xref>, the volume fractions had increased the same way as UO<sub>2</sub>. From <xref ref-type="fig" rid="F7">Figures 7D&#x2013;F</xref>, the volume fraction of &#x3b2;-phase on cladding inner-surface had increased from <inline-formula id="inf54">
<mml:math id="m62">
<mml:mrow>
<mml:mn>1.8</mml:mn>
<mml:mo>&#xd7;</mml:mo>
<mml:msup>
<mml:mrow>
<mml:mn>10</mml:mn>
</mml:mrow>
<mml:mrow>
<mml:mo>&#x2212;</mml:mo>
<mml:mn>7</mml:mn>
</mml:mrow>
</mml:msup>
</mml:mrow>
</mml:math>
</inline-formula> to <inline-formula id="inf55">
<mml:math id="m63">
<mml:mrow>
<mml:mn>2.1</mml:mn>
<mml:mo>&#xd7;</mml:mo>
<mml:msup>
<mml:mrow>
<mml:mn>10</mml:mn>
</mml:mrow>
<mml:mrow>
<mml:mo>&#x2212;</mml:mo>
<mml:mn>6</mml:mn>
</mml:mrow>
</mml:msup>
</mml:mrow>
</mml:math>
</inline-formula> when the coefficient decreased from 1.0 to 0.8. In <xref ref-type="fig" rid="F6">Figures 6B,D</xref>, the volume fraction of &#x3b2;-phase for UO<sub>2</sub>-10vol%BeO on cladding inner-surface had increased from <inline-formula id="inf56">
<mml:math id="m64">
<mml:mrow>
<mml:mn>2.1</mml:mn>
<mml:mo>&#xd7;</mml:mo>
<mml:msup>
<mml:mrow>
<mml:mn>10</mml:mn>
</mml:mrow>
<mml:mrow>
<mml:mo>&#x2212;</mml:mo>
<mml:mn>6</mml:mn>
</mml:mrow>
</mml:msup>
</mml:mrow>
</mml:math>
</inline-formula> to <inline-formula id="inf57">
<mml:math id="m65">
<mml:mrow>
<mml:mn>3.9</mml:mn>
<mml:mo>&#xd7;</mml:mo>
<mml:msup>
<mml:mrow>
<mml:mn>10</mml:mn>
</mml:mrow>
<mml:mrow>
<mml:mo>&#x2212;</mml:mo>
<mml:mn>4</mml:mn>
</mml:mrow>
</mml:msup>
</mml:mrow>
</mml:math>
</inline-formula> when the coefficient decreased from 0.8 to 0.6. Compared with UO<sub>2</sub>, the volume fractions for UO<sub>2</sub>-10vol%BeO are much lower, and they are off by three orders of magnitude.</p>
<fig id="F6" position="float">
<label>FIGURE 6</label>
<caption>
<p>Volume fractions of &#x3b2;-phase on cladding inner surface and outer-surface, changing with the heat transfer coefficient multiplied by a number smaller than 1, <bold>(A)</bold> 0.6 for UO<sub>2</sub> and Zircaloy-4, <bold>(B)</bold> 0.6 for UO<sub>2</sub>-10vol%BeO and Zircaloy-4, <bold>(C)</bold> 0.8 for UO<sub>2</sub> and Zircaloy-4, <bold>(D)</bold> 0.8 for UO<sub>2</sub>-10vol%BeO and Zircaloy-4, <bold>(E)</bold> 1.0 for UO<sub>2</sub> and Zircaloy-4, <bold>(F)</bold> 1.0 for UO<sub>2</sub>-10vol%BeO and Zircaloy-4.</p>
</caption>
<graphic xlink:href="fenrg-09-667419-g006.tif"/>
</fig>
<fig id="F7" position="float">
<label>FIGURE 7</label>
<caption>
<p>Volume fraction of &#x3b2;-phase on cladding inner and outer surface with power linear rate 60,000&#xa0;W/m, gap size 1e&#x2013;7&#xa0;m, temperature at the extremities of fuel element 1500&#xa0;K and the number multiplying the heat transfer coefficient 0.4, <bold>(A)</bold> for UO<sub>2</sub> and Zircaloy-4, <bold>(B)</bold> for UO<sub>2</sub>-10vol%BeO and Zircaloy-4.</p>
</caption>
<graphic xlink:href="fenrg-09-667419-g007.tif"/>
</fig>
<p>From all the figures above (i.e.,&#x20;<xref ref-type="fig" rid="F3">Figures 3</xref>&#x2013;<xref ref-type="fig" rid="F6">6</xref>), we found that the highest volume fractions of &#x3b2;-phase are only <inline-formula id="inf58">
<mml:math id="m66">
<mml:mrow>
<mml:mn>0.052</mml:mn>
</mml:mrow>
</mml:math>
</inline-formula> for UO<sub>2</sub> and <inline-formula id="inf59">
<mml:math id="m67">
<mml:mrow>
<mml:mn>3.9</mml:mn>
<mml:mo>&#xd7;</mml:mo>
<mml:msup>
<mml:mrow>
<mml:mn>10</mml:mn>
</mml:mrow>
<mml:mrow>
<mml:mo>&#x2212;</mml:mo>
<mml:mn>4</mml:mn>
</mml:mrow>
</mml:msup>
</mml:mrow>
</mml:math>
</inline-formula> for UO<sub>2</sub>-10vol%BeO, which are still not high enough to reach the significant phase transformation interval. To simulate a severe condition, we reset the four parameters mentioned above: the linear power rate, the temperature at the extremities of the fuel element, the gap size, and the heat transfer coefficient to simulate&#x20;again.</p>
<p>This time we set the linear power rate to 60,000&#xa0;W/m according to Westinghouse Technology Systems Manual by NRC (<xref ref-type="bibr" rid="B4">The U.S. Nuclear Regulatory Commission, 2011</xref>). We decreased the gap size from 8e&#x2013;7 to 1e&#x2013;7&#xa0;m because we have seen a relatively significant influence of gap size on the volume fraction of the new phase (&#x3b2;-phase). We can also decrease the coefficient of heat transfer by multiplying a number smaller (this time, we choose 0.4) for the same reason. Nevertheless, we could keep the temperature at the extremities of fuel element 1500&#xa0;K because it seems that this temperature has little influence on the volume fraction of the &#x3b2;-phase. The results are shown&#x20;below.</p>
<p>As we can see, the volume fraction of the &#x3b2;-phase on cladding inner-surface for UO<sub>2</sub> in <xref ref-type="fig" rid="F7">Figure&#x20;7A</xref> has reached nearly 0.4, which means the inner surface of cladding had reached the significant phase transformation interval.</p>
<p>The result for UO<sub>2</sub>-10vol%BeO in <xref ref-type="fig" rid="F7">Figure&#x20;7B</xref>, comparing with the results before (i.e.,&#x20;<xref ref-type="fig" rid="F3">Figures 3</xref>&#x2013;<xref ref-type="fig" rid="F6">6</xref>), showed a significant increase in the volume fraction of &#x3b2;-phase, reaching nearly 0.01. However, the volume fraction is still minimal, which showed that the phase transformation did not significantly occur on both the inner and outer surfaces of cladding for UO<sub>2</sub>-10vol%BeO.</p>
<p>To see more clearly the variation of the &#x3b2;-phase volume fraction with axial direction on cladding inner-surface, in <xref ref-type="fig" rid="F8">Figures 8A,B</xref>, we found that the &#x3b2;-phase volume fraction decreases with the cladding radius increase.</p>
<fig id="F8" position="float">
<label>FIGURE 8</label>
<caption>
<p>Volume fraction of &#x3b2;-phase from cladding inner surface to outer-surface with the same parameter setting in <xref ref-type="fig" rid="F7">Figure&#x20;7</xref> for <bold>(A)</bold> UO<sub>2</sub> and Zircaloy-4, <bold>(B)</bold> UO<sub>2</sub>-10vol%BeO and Zircaloy-4.</p>
</caption>
<graphic xlink:href="fenrg-09-667419-g008.tif"/>
</fig>
</sec>
<sec id="s4">
<title>Analysis and Discussion</title>
<p>As seen in the results above, we found that all parameters have an evident influence on the volume fraction of the favored phase except the temperature at the extremities of the fuel element, which has little impact. In the results of <xref ref-type="fig" rid="F3">Figures 3</xref>&#x2013;<xref ref-type="fig" rid="F6">6</xref>, the highest volume fractions of &#x3b2;-phase are 0.052 for UO<sub>2</sub> and <inline-formula id="inf60">
<mml:math id="m68">
<mml:mrow>
<mml:mn>3.9</mml:mn>
<mml:mo>&#xd7;</mml:mo>
<mml:msup>
<mml:mrow>
<mml:mn>10</mml:mn>
</mml:mrow>
<mml:mrow>
<mml:mo>&#x2212;</mml:mo>
<mml:mn>4</mml:mn>
</mml:mrow>
</mml:msup>
</mml:mrow>
</mml:math>
</inline-formula> for UO<sub>2</sub>-10vol%BeO, respectively. These two values have a significant difference of two orders of magnitude, which showed the BeO addition&#x27;s significant influence on the fuel-cladding system. For the last case in <xref ref-type="fig" rid="F7">Figure&#x20;7</xref>, the volume fractions of &#x3b2;-phase on cladding inner-surface are around 0.39 for UO<sub>2</sub> and 0.0094 for UO<sub>2</sub>-10vol%BeO, where there is still a significant difference between&#x20;them.</p>
<p>According to the results in (<xref ref-type="bibr" rid="B17">Liu et&#x20;al., 2015</xref>), the addition of BeO decreased fuel temperature by increasing the fuel thermal conductivity. However, we found that the temperature distribution in the cladding (not the fuel) for both UO<sub>2</sub> and UO<sub>2</sub>-10vol%BeO is very close to our results. Although the temperature is close, the volume fraction has a significant difference. According to Massih in (<xref ref-type="bibr" rid="B22">Massih, 2009</xref>), the heating rate Q affects the position of the transformed volume fraction. More specifically, when the absolute value of Q increases, the graph of volume fraction of &#x3b2;-phase will move to a higher temperature position. Thus from our results presented in <xref ref-type="fig" rid="F3">Figures 3</xref>&#x2013;<xref ref-type="fig" rid="F7">7</xref>, we can deduce that the heating rate Q for UO<sub>2</sub>-10vol%BeO is higher than that for UO<sub>2</sub> because the volume fraction for UO<sub>2</sub>-10vol%BeO is lower than that for UO<sub>2</sub> under the similar temperature. We may also deduce that the addition of BeO affects the temperature variation, which is the heating rate&#x20;Q.</p>
</sec>
<sec id="s5">
<title>Conclusion and Prospects</title>
<p>In summary, this model simulates the phase transformation by presenting the volume fraction of the favored phase <inline-formula id="inf61">
<mml:math id="m69">
<mml:mrow>
<mml:mrow>
<mml:mo>(</mml:mo>
<mml:mrow>
<mml:mi mathvariant="normal">&#x3b2;-phase</mml:mi>
</mml:mrow>
<mml:mo>)</mml:mo>
</mml:mrow>
</mml:mrow>
</mml:math>
</inline-formula> on the cladding inner and outer surfaces. In the case of <xref ref-type="fig" rid="F7">Figure&#x20;7</xref>, which has the most severe LOCA conditions in all the groups of calculations, the addition of 10vol%BeO in the UO<sub>2</sub> fuel decreased the phase transformation effect a lot, which shows that the addition of BeO may increase the rate parameter for temperature under heating. All the results for UO<sub>2</sub>-10vol%BeO showed that no significant phase transformation was observed in the Zircaloy-4 cladding with UO<sub>2</sub>-BeO enhanced thermal conductivity nuclear fuel during the existing loss-of-coolant accident conditions.</p>
<p>For further study on phase transformation behavior in Zircaloy-4 cladding with the UO<sub>2</sub>-BeO enhanced thermal conductivity nuclear fuel, adjusting parameters to simulate a more realistic loss-of-coolant accident would be the right choice. In this model, we have used a constant to represent the variation of hydrogen concentration. To analog a more realistic phase transformation, implanting the model of hydrogen pickup and ydride formation would be beneficial. The influence of excess oxygen due to oxidation is another important factor affecting phase transformation behavior in Zircaloy-4 cladding and needs to be modeled in the future&#x20;work.</p>
<table-wrap id="T2" position="float">
<label>TABLE 2</label>
<caption>
<p>Constants for <xref ref-type="sec" rid="s9">Supplementary Equation (S14)</xref>.</p>
</caption>
<table>
<thead valign="top">
<tr>
<th align="left">BeO</th>
<th align="left"/>
<th align="center">A</th>
<th align="center">B</th>
<th align="center">E</th>
<th align="center">F</th>
</tr>
<tr>
<th align="left">
<italic>wt%</italic>
</th>
<th align="center">
<italic>vol%</italic>
</th>
<th align="center">
<italic>mK/W</italic>
</th>
<th align="center">
<italic>m/W</italic>
</th>
<th align="center">
<italic>mK/W</italic>
</th>
<th align="center">
<italic>K</italic>
</th>
</tr>
</thead>
<tbody valign="top">
<tr>
<td align="left">0</td>
<td align="char" char=".">0</td>
<td align="char" char=".">0.0452</td>
<td align="center">2.46e&#x2212;4</td>
<td align="center">3.5e9</td>
<td align="center">16,361</td>
</tr>
<tr>
<td align="left">0.6</td>
<td align="char" char=".">2.14558</td>
<td align="char" char=".">0.01752</td>
<td align="center">1.92e&#x2212;4</td>
<td align="center">3.5e9</td>
<td align="center">16,361</td>
</tr>
<tr>
<td align="left">1.2</td>
<td align="char" char=".">4.22546</td>
<td align="char" char=".">0.007068</td>
<td align="center">1.95e&#x2212;4</td>
<td align="center">3.5e9</td>
<td align="center">16,361</td>
</tr>
<tr>
<td align="left">2.97</td>
<td align="char" char=".">10</td>
<td align="char" char=".">0.00775</td>
<td align="center">1.96353e&#x2212;4</td>
<td align="center">3.5e9</td>
<td align="center">16.361</td>
</tr>
<tr>
<td align="left">13.6</td>
<td align="char" char=".">36.3777</td>
<td align="char" char=".">&#x2212;0.01378</td>
<td align="center">8.21e&#x2212;5</td>
<td align="center">3.5e9</td>
<td align="center">16,631</td>
</tr>
</tbody>
</table>
</table-wrap>
</sec>
</body>
<back>
<sec id="s6">
<title>Data Availability Statement</title>
<p>The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.</p>
</sec>
<sec id="s7">
<title>Author Contributions</title>
<p>The work is mainly done by WL. LQ contributed to the accomplishment of this work, and WZ is the advisor of&#x20;WL.</p>
</sec>
<sec sec-type="COI-statement" id="s8">
<title>Conflict of Interest</title>
<p>The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.</p>
</sec>
<ack>
<p>The financial support from Nuclear Power Technology Innovation Center of China (No. 45000-41020012), the Fundamental Research Funds for the Central Universities of China (No. 45000-18841210), the International Sci &#x26; Tech Cooperation Program of Guangdong Province (No. 2019A050510022), and Guangdong Major Project of Basic and Applied Basic Research (No. 2019B030302011) is highly appreciated.</p>
</ack>
<sec id="s9">
<title>Supplementary Material</title>
<p>The Supplementary Material for this article can be found online at: <ext-link ext-link-type="uri" xlink:href="https://www.frontiersin.org/articles/10.3389/fenrg.2021.667419/full#supplementary-material">https://www.frontiersin.org/articles/10.3389/fenrg.2021.667419/full&#x23;supplementary-material</ext-link>
</p>
<supplementary-material xlink:href="DataSheet1.docx" id="SM1" mimetype="application/docx" xmlns:xlink="http://www.w3.org/1999/xlink"/>
</sec>
<ref-list>
<title>References</title>
<ref id="B1">
<citation citation-type="book">
<person-group person-group-type="author">
<name>
<surname>Brachet</surname>
<given-names>J.&#x20;C.</given-names>
</name>
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