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  <front>
    <journal-meta>
      <journal-id journal-id-type="publisher-id">79</journal-id>
      <journal-id journal-id-type="index">urn:lsid:arphahub.com:pub:D015427E-53F6-553C-9279-2E51CD684756</journal-id>
      <journal-title-group>
        <journal-title xml:lang="en">Nuclear Energy and Technology</journal-title>
        <abbrev-journal-title xml:lang="en">NUCET</abbrev-journal-title>
      </journal-title-group>
      <issn pub-type="epub">2452-3038</issn>
      <publisher>
        <publisher-name>National Research Nuclear University MEPhI (Moscow Engineering Physics Institute)</publisher-name>
      </publisher>
    </journal-meta>
    <article-meta>
      <article-id pub-id-type="doi">10.3897/nucet.10.129596</article-id>
      <article-id pub-id-type="publisher-id">129596</article-id>
      <article-categories>
        <subj-group subj-group-type="heading">
          <subject>Research Article</subject>
        </subj-group>
        <subj-group subj-group-type="scientific_subject">
          <subject>Nuclear physics</subject>
          <subject> Fusion and Radiation application</subject>
        </subj-group>
      </article-categories>
      <title-group>
        <article-title>﻿Interaction of iron melt with tungsten and WFe composite structure evolution</article-title>
      </title-group>
      <contrib-group content-type="authors">
        <contrib contrib-type="author" corresp="yes">
          <name name-style="western">
            <surname>Popov</surname>
            <given-names>Nikita</given-names>
          </name>
          <email xlink:type="simple">nspopov@mephi.ru</email>
          <uri content-type="orcid">https://orcid.org/0000-0003-2551-588X</uri>
          <xref ref-type="aff" rid="A1">1</xref>
        </contrib>
        <contrib contrib-type="author" corresp="no">
          <name name-style="western">
            <surname>Suchkov</surname>
            <given-names>Alexey</given-names>
          </name>
          <xref ref-type="aff" rid="A1">1</xref>
        </contrib>
        <contrib contrib-type="author" corresp="no">
          <name name-style="western">
            <surname>Zharkov</surname>
            <given-names>Mikhail</given-names>
          </name>
          <xref ref-type="aff" rid="A1">1</xref>
          <xref ref-type="aff" rid="A2">2</xref>
        </contrib>
        <contrib contrib-type="author" corresp="no">
          <name name-style="western">
            <surname>Kirillova</surname>
            <given-names>Veronika</given-names>
          </name>
          <xref ref-type="aff" rid="A1">1</xref>
        </contrib>
        <contrib contrib-type="author" corresp="no">
          <name name-style="western">
            <surname>Bazhenov</surname>
            <given-names>Alexander</given-names>
          </name>
          <xref ref-type="aff" rid="A1">1</xref>
        </contrib>
        <contrib contrib-type="author" corresp="no">
          <name name-style="western">
            <surname>Fedotov</surname>
            <given-names>Ivan</given-names>
          </name>
          <xref ref-type="aff" rid="A1">1</xref>
        </contrib>
        <contrib contrib-type="author" corresp="no">
          <name name-style="western">
            <surname>Bajenova</surname>
            <given-names>Irina</given-names>
          </name>
          <uri content-type="orcid">https://orcid.org/0000-0003-0758-3141</uri>
          <xref ref-type="aff" rid="A3">3</xref>
        </contrib>
        <contrib contrib-type="author" corresp="no">
          <name name-style="western">
            <surname>Khvan</surname>
            <given-names>Alexandra</given-names>
          </name>
          <xref ref-type="aff" rid="A3">3</xref>
        </contrib>
        <contrib contrib-type="author" corresp="no">
          <name name-style="western">
            <surname>Kozlov</surname>
            <given-names>Ilya</given-names>
          </name>
          <xref ref-type="aff" rid="A1">1</xref>
          <xref ref-type="aff" rid="A4">4</xref>
        </contrib>
        <contrib contrib-type="author" corresp="no">
          <name name-style="western">
            <surname>Vertkov</surname>
            <given-names>Alexey</given-names>
          </name>
          <xref ref-type="aff" rid="A2">2</xref>
        </contrib>
        <contrib contrib-type="author" corresp="no">
          <name name-style="western">
            <surname>Sevryukov</surname>
            <given-names>Oleg</given-names>
          </name>
          <xref ref-type="aff" rid="A1">1</xref>
        </contrib>
      </contrib-group>
      <aff id="A1">
        <label>1</label>
        <addr-line content-type="verbatim">National Research Nuclear University MEPhI (Moscow Engineering Physics Institute), Kashirskoye Shosse, 31, 115409 Moscow, Russia</addr-line>
        <institution>National Research Nuclear University MEPhI</institution>
        <addr-line content-type="city">Moscow</addr-line>
        <country>Russia</country>
      </aff>
      <aff id="A2">
        <label>2</label>
        <addr-line content-type="verbatim">Joint-Stock Company “N.A. Dollezhall Research and Development Institute of Power Engineering”, (JSC “NIKIET”), Malaya Krasnoselskaya 2/8, 107140, Moscow, Russia</addr-line>
        <institution>Joint-Stock Company “N.A. Dollezhall Research and Development Institute of Power Engineering”</institution>
        <addr-line content-type="city">Moscow</addr-line>
        <country>Russia</country>
      </aff>
      <aff id="A3">
        <label>3</label>
        <addr-line content-type="verbatim">Faculty of Chemistry, Lomonosov Moscow State University, 1-3 Leninskiye Gory, 119991, Moscow, Russia</addr-line>
        <institution>Lomonosov Moscow State University</institution>
        <addr-line content-type="city">Moscow</addr-line>
        <country>Russia</country>
      </aff>
      <aff id="A4">
        <label>4</label>
        <addr-line content-type="verbatim">National Research Center “Kurchatov Institute”, Moscow 123182, Russia</addr-line>
        <institution>National Research Center “Kurchatov Institute”</institution>
        <addr-line content-type="city">Moscow</addr-line>
        <country>Russia</country>
      </aff>
      <author-notes>
        <fn fn-type="corresp">
          <p>Corresponding author: Nikita Popov (<ext-link xlink:href="mailto:NSPopov@mephi.ru" ext-link-type="uri" xlink:type="simple">NSPopov@mephi.ru</ext-link>)</p>
        </fn>
        <fn fn-type="edited-by">
          <p>Academic editor: Tan Xiaoyue</p>
        </fn>
      </author-notes>
      <pub-date pub-type="collection">
        <year>2024</year>
      </pub-date>
      <pub-date pub-type="epub">
        <day>27</day>
        <month>08</month>
        <year>2024</year>
      </pub-date>
      <volume>10</volume>
      <issue>3</issue>
      <fpage>189</fpage>
      <lpage>198</lpage>
      <uri content-type="arpha" xlink:href="http://openbiodiv.net/1689EAF6-10D8-584F-90E4-A927FB418E5C">1689EAF6-10D8-584F-90E4-A927FB418E5C</uri>
      <history>
        <date date-type="received">
          <day>12</day>
          <month>06</month>
          <year>2024</year>
        </date>
        <date date-type="accepted">
          <day>07</day>
          <month>08</month>
          <year>2024</year>
        </date>
      </history>
      <permissions>
        <copyright-statement>Nikita Popov, Alexey Suchkov, Mikhail Zharkov, Veronika Kirillova, Alexander Bazhenov, Ivan Fedotov, Irina Bajenova, Alexandra Khvan, Ilya Kozlov, Alexey Vertkov, Oleg Sevryukov</copyright-statement>
        <license license-type="creative-commons-attribution" xlink:href="http://creativecommons.org/licenses/by/4.0/" xlink:type="simple">
          <license-p>This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.</license-p>
        </license>
      </permissions>
      <abstract>
        <label>﻿Abstract</label>
        <p>Development of new plasma facing components (<abbrev xlink:title="plasma facing components" id="ABBRID0EQG">PFC</abbrev>) draw attention of numerous scientific groups in fusion energy field. Tungsten as a main <abbrev xlink:title="plasma facing components" id="ABBRID0EUG">PFC</abbrev> material main have poor machinability, thus various designs were proposed to overcome this problem. However, such technologies as functional graded layers, sintering and additive technologies are limited in production size and have low cost-efficiency. This research considers the alternative approach of steel melt injection or melt infiltration of tungsten mesh. The results obtained establish the mechanism of phase evolution during interaction of solid W with liquid steel and iron. Energy dispersive spectroscopy, X-ray diffraction and Thermocalc calculations used to analyze the phase composition of tungsten wetted with various steels and pure iron. Results show that interaction rate significantly depends on melt temperature and overheating above its liquidus. Then the overheating exceeds 150 °C erosion of tungsten occur.</p>
      </abstract>
      <kwd-group>
        <label>Keywords</label>
        <kwd>iron, steel, tungsten, composite, melting, wetting angle, high temperature interaction, intermetallic compounds, armor block, heat transfer</kwd>
      </kwd-group>
      <funding-group>
        <award-group>
          <funding-source>
            <named-content content-type="funder_name">Russian Science Foundation</named-content>
            <named-content content-type="funder_identifier">501100006769</named-content>
            <named-content content-type="funder_doi">http://doi.org/10.13039/501100006769</named-content>
          </funding-source>
        </award-group>
      </funding-group>
    </article-meta>
  </front>
  <body>
    <sec sec-type="﻿Introduction" id="SECID0E3G">
      <title>﻿Introduction</title>
      <p>Modern fusion facilities face the problem of erosion and sputtering of plasma facing components (<abbrev xlink:title="plasma facing components" id="ABBRID0ECH">PFC</abbrev>) material under thermal loads, which cause plasma contamination. Tungsten is proposed as a divertor material for International Thermonuclear Reactor (<abbrev xlink:title="International Thermonuclear Reactor" id="ABBRID0EGH">ITER</abbrev>) due to its high melting temperature, which allows it to withstand thermal loads up to 20 MW/m<sup>2</sup> (<xref ref-type="bibr" rid="B15">Hirai et al. 2005</xref>; <xref ref-type="bibr" rid="B31">Schoofs and Gorley 2019</xref>; <xref ref-type="bibr" rid="B10">Gago et al. 2020</xref>). Moreover, beryllium as the <abbrev xlink:title="International Thermonuclear Reactor" id="ABBRID0EYH">ITER</abbrev> first wall material will be replaced by tungsten due to its high sputtering rate (<xref ref-type="bibr" rid="B13">Guseva et al. 1999</xref>). However, some problems with tungsten armored blocks need to be resolved before their industrial application in the next generation fusion reactors.</p>
      <p>High thermal conductivity of tungsten (<xref ref-type="bibr" rid="B33">Tolias 2017</xref>) provides high efficiency of heat transfer from the plasma-facing surface to the coolant. However, poor machinability of tungsten increases production costs. Joining tungsten blocks to the basic structure of a fusion facility by high-temperature brazing requires high precision during the joining process. Experience in brazing technology shows that the gaps between materials should be about few dozens of microns (<xref ref-type="bibr" rid="B2">Bachurina et al. 2021a</xref>, <xref ref-type="bibr" rid="B3">2021b</xref>; <xref ref-type="bibr" rid="B27">Penyaz et al. 2021</xref>). These production difficulties lead to a more complex design of a fusion facility. Alternative way to join W is hot isostatic pressing also require precision to provide acceptable performance (<xref ref-type="bibr" rid="B30">Saito et al. 2002</xref>).</p>
      <p>On the other hand, Reduced Activation Ferritic-Martensitic (<abbrev xlink:title="Reduced Activation Ferritic-Martensitic" id="ABBRID0EZAAC">RAFM</abbrev>) steel and austenitic steel 316LN are commonly used as a base structural material for the <abbrev xlink:title="International Thermonuclear Reactor" id="ABBRID0E4AAC">ITER</abbrev>-like facilities. Steel can be easily cut, welded, and brazed. A combination of high thermal conductivity and machinability could be achieved in a composite material. In terms of technological simplicity, the WFe composite should consist of tungsten fiber, which transfers the heat, and an iron-based matrix, which allows the underlying structure to be cut and welded.</p>
      <p>Another important point is that capillary porous systems (<abbrev xlink:title="capillary porous systems" id="ABBRID0EDBAC">CPS</abbrev>), commonly made from various tungsten or molybdenum meshes, require a base material (<xref ref-type="bibr" rid="B22">Lyublinski et al. 2016</xref>). The Fig. <xref ref-type="fig" rid="F1">1</xref> shows a schematic representation of WFe composite in tokamak construction with <abbrev xlink:title="capillary porous systems" id="ABBRID0EPBAC">CPS</abbrev> and without. The WFe composite design implies that the plasma-facing surface of <abbrev xlink:title="plasma facing components" id="ABBRID0ETBAC">PFC</abbrev> made of tungsten or <abbrev xlink:title="capillary porous systems" id="ABBRID0EXBAC">CPS</abbrev> will absorb heat load and transfer it to underlying WFe composite, which in turn transfer it to coolant. The liquid lithium technique show high performance in numerous experiments (<xref ref-type="bibr" rid="B41">Zuo et al. 2011</xref>; <xref ref-type="bibr" rid="B39">Yang et al. 2017</xref>; <xref ref-type="bibr" rid="B1">Andruczyk et al. 2020</xref>). As <abbrev xlink:title="capillary porous systems" id="ABBRID0EHCAC">CPS</abbrev> is based on tungsten mesh, the WFe composite is a suitable base structure for it.</p>
      <fig id="F1" position="float" orientation="portrait">
        <object-id content-type="doi">10.3897/nucet.10.129596.figure1</object-id>
        <object-id content-type="arpha">040BE348-D830-5CC4-ADE0-329EDA99052E</object-id>
        <label>Figure 1.</label>
        <caption>
          <p>Schematic representation of WFe composite in <abbrev xlink:title="plasma facing components" id="ABBRID0ETCAC">PFC</abbrev>.</p>
        </caption>
        <graphic xlink:href="nucet-10-e129596-g001.jpg" position="float" orientation="portrait" xlink:type="simple" id="oo_1121824.jpg">
          <uri content-type="original_file">https://binary.pensoft.net/fig/1121824</uri>
        </graphic>
      </fig>
      <p>The WFe composite is designed to provide better performance than conventional copper and bronze elements, which unable to withstand high heat loads and radiation damage (<xref ref-type="bibr" rid="B9">Fabritsiev et al. 1996</xref>). The composite structure is compatible with liquid metal coolants with high thermal conductivity such as Li (<xref ref-type="bibr" rid="B25">Meng et al. 2018</xref>). To sum up, WFe could provide the thermal conductivity at the level of bronze and higher strength, while compatibility with liquid metal coolants allow absorbing higher heat fluxes.</p>
      <p>The combination of W and steel in one material is a poorly developed topic primarily due to great difference between their CTE (α (W) = 4.4 × 10<sup>-6</sup> K<sup>-1</sup> and α (<abbrev xlink:title="Reduced Activation Ferritic-Martensitic" id="ABBRID0EMDAC">RAFM</abbrev>) = 12.7 × 10<sup>-6</sup> K<sup>-1</sup> (<xref ref-type="bibr" rid="B26">Paúl et al. 2006</xref>) and brittle intermetallic compounds (<abbrev xlink:title="intermetallic compounds" id="ABBRID0EYDAC">IMC</abbrev>) formation. In order to overcome this problem, materials with functional graded layers produced by plasma or magnetron sputtering have been proposed in works (<xref ref-type="bibr" rid="B36">Weber et al. 2013</xref>; <xref ref-type="bibr" rid="B32">Tan et al. 2019</xref>; <xref ref-type="bibr" rid="B11">Ganesh et al. 2023</xref>). This technique provides high adhesion between layers, yet low tolerance to cyclic loads cause failure after just a few cycles (<xref ref-type="bibr" rid="B28">Qu et al. 2019</xref>). In addition sintered layers of different materials are prone to interact due to diffusion with intermetallic Fe<sub>7</sub>W<sub>6</sub> formation (<xref ref-type="bibr" rid="B14">Heuer et al. 2020</xref>).</p>
      <p>Tungsten and steel powders joined by spark plasma sintering into a bulk material promise high thermal properties with minimal interaction between materials. Some positive results have been obtained in this field (<xref ref-type="bibr" rid="B5">Chen et al. 2018</xref>; <xref ref-type="bibr" rid="B18">Koller et al. 2018</xref>). However, Fe<sub>2</sub>W type IMCs have been detected in the interaction layer between powder particles, which reduces thermal conductivity and mechanical properties. In general, sintering and functional graded layer approaches have low cost-efficiency and are limited in product size.</p>
      <p>Additive technologies have a low production speed, but the current technology level allows us to control the structure of the material with high precision. Laser metal deposition of Fe and W powders was used to fabricate a WFe composite in the work (<xref ref-type="bibr" rid="B4">Chen et al. 2021</xref>). Microstructure investigation shows that numerous tungsten particles surrounded by an Fe<sub>7</sub>W<sub>6</sub> layer are embedded in an iron matrix enriched with tungsten. Fe<sub>2</sub>W intermetallic compounds nucleate in the steel matrix only upon multiple heating. Hence, it can be concluded that a short-term manufacturing process allows us to avoid the formation of an intermetallic phase.</p>
      <p>The tungsten fiber mesh forms a capillary structure that can be easily filled with liquid steel. Infiltration with a liquid phase leads to a high interaction rate between materials. Alloys with low melting point and high oxidation resistance can be cast via different methods. Recently, the high-pressure die casting method has been significantly improved by the total vacuum process high-pressure die casting (<abbrev xlink:title="total vacuum process high-pressure die casting" id="ABBRID0EOFAC">EVP HPDC</abbrev>) (<xref ref-type="bibr" rid="B12">Gao et al. 2021</xref>). This technology makes it possible to obtain oxygen-sensitive amorphous Zr-based alloys with high glass-forming ability. The main difficulty for steel casting using <abbrev xlink:title="total vacuum process high-pressure die casting" id="ABBRID0EWFAC">EVP HPDC</abbrev> is the shot sleeve and die material, which will suffer from overheated steel melt. The main advantage of this technology is a high cooling rate almost high as in magnetic-pulse welding (<xref ref-type="bibr" rid="B20">Lazurenko et al. 2024</xref>).</p>
      <p>The capillary forces could simplify the casting technique. Melt infiltration widely used to produce composites with ceramic or metal reinforcement (<xref ref-type="bibr" rid="B34">Toy and Scott 1990</xref>; <xref ref-type="bibr" rid="B6">Dandliker et al. 1998</xref>; <xref ref-type="bibr" rid="B7">De Jongh and Eggenhuisen 2013</xref>). When the melt interacts with the tungsten mesh, the liquid metal will be drawn in by capillary forces, forming a bulk solid structure reinforced with tungsten. The technology described above is similar to melt infiltration. Such technology have been already tested on W-Cu material for mock-ups of the limiter (<xref ref-type="bibr" rid="B8">De Luca et al. 2023</xref>).</p>
      <p>The capillary force depends on the wetting characteristics of the liquid steel and the tungsten. The study of interaction between the liquid and solid materials and the following phase formation at high temperatures is important for the development of melt infiltration technology. The wetting behavior of steel melt on metal materials is poorly investigated. Few works consider the ceramic substrates wetted by steel and iron (<xref ref-type="bibr" rid="B37">Xuan et al. 2015</xref>; <xref ref-type="bibr" rid="B38">Yan et al. 2018</xref>; <xref ref-type="bibr" rid="B21">Long et al. 2024</xref>).</p>
      <p>An attempt to manufacture the steel matrix strengthened with tungsten wire was made in (<xref ref-type="bibr" rid="B19">Kumar 2013</xref>). Casting at 1550 °C cause significant erosion and tungsten dissolution in steel melt. Due to the nature of casting various zones of composite have different structure with relatively thin and thick intermetallic layer. Thus, the critical temperature of melt when an interaction become intensive should be defined to achieve the desirable structure.</p>
      <p>In this work, we made an attempt to investigate the features of the interaction at high temperatures of pure iron, several grades of steel, and a pure tungsten substrate. The data obtained is crucial for the melt infiltration technology, with regard to the WFe composite production.</p>
    </sec>
    <sec sec-type="materials|methods" id="SECID0EFHAC">
      <title>﻿Materials and methods</title>
      <p>The investigation consists of two stages: wetting measurement and high-temperature interaction. The list of materials and their chemical composition according to manufacturer certificate given in Table <xref ref-type="table" rid="T1">1</xref>. In all the experiments, pure <abbrev xlink:title="International Thermonuclear Reactor" id="ABBRID0EPHAC">ITER</abbrev>-grade tungsten was used as the base solid material. A simplified setup was used to represent the interaction between solid W and liquid steel during melt infiltration. The schematic experimental setups of stages 1 and 2 are shown in Fig. <xref ref-type="fig" rid="F2">2</xref>.</p>
      <table-wrap id="T1" position="float" orientation="portrait">
        <label>Table 1.</label>
        <caption>
          <p>Materials chemical composition</p>
        </caption>
        <table id="TID0EH6AG" rules="all">
          <tbody>
            <tr>
              <th rowspan="2" colspan="1">Material</th>
              <th rowspan="1" colspan="8">Content, wt.%</th>
            </tr>
            <tr>
              <th rowspan="1" colspan="1">Fe</th>
              <th rowspan="1" colspan="1">Cr</th>
              <th rowspan="1" colspan="1">С</th>
              <th rowspan="1" colspan="1">Ni</th>
              <th rowspan="1" colspan="1">Ti</th>
              <th rowspan="1" colspan="1">Mo</th>
              <th rowspan="1" colspan="1">W</th>
              <th rowspan="1" colspan="1">Other</th>
            </tr>
            <tr>
              <td rowspan="1" colspan="1">Fe</td>
              <td rowspan="1" colspan="1">&gt;99.96</td>
              <td rowspan="1" colspan="1">–</td>
              <td rowspan="1" colspan="1">&lt;0.035</td>
              <td rowspan="1" colspan="1">–</td>
              <td rowspan="1" colspan="1">–</td>
              <td rowspan="1" colspan="1">–</td>
              <td rowspan="1" colspan="1">–</td>
              <td rowspan="1" colspan="1">–</td>
            </tr>
            <tr>
              <td rowspan="1" colspan="1">AISI 420</td>
              <td rowspan="1" colspan="1">Bal.</td>
              <td rowspan="1" colspan="1">12–14</td>
              <td rowspan="1" colspan="1">0.16–0.25</td>
              <td rowspan="1" colspan="1">&lt;0.6</td>
              <td rowspan="1" colspan="1">–</td>
              <td rowspan="1" colspan="1">–</td>
              <td rowspan="1" colspan="1">–</td>
              <td rowspan="1" colspan="1">&lt;0.6Mn</td>
            </tr>
            <tr>
              <td rowspan="1" colspan="1">EK-181</td>
              <td rowspan="1" colspan="1">Bal.</td>
              <td rowspan="1" colspan="1">10–12</td>
              <td rowspan="1" colspan="1">0.12–0.18</td>
              <td rowspan="1" colspan="1">–</td>
              <td rowspan="1" colspan="1">0.05</td>
              <td rowspan="1" colspan="1">0.01</td>
              <td rowspan="1" colspan="1">2</td>
              <td rowspan="1" colspan="1">0.006B; 0.2–0.4V; 0.05–0.2Ta</td>
            </tr>
            <tr>
              <td rowspan="1" colspan="1">AISI 316L</td>
              <td rowspan="1" colspan="1">Bal.</td>
              <td rowspan="1" colspan="1">16–18</td>
              <td rowspan="1" colspan="1">0.02</td>
              <td rowspan="1" colspan="1">10–14</td>
              <td rowspan="1" colspan="1">0.05</td>
              <td rowspan="1" colspan="1">2–3</td>
              <td rowspan="1" colspan="1">–</td>
              <td rowspan="1" colspan="1">–</td>
            </tr>
            <tr>
              <td rowspan="1" colspan="1">W</td>
              <td rowspan="1" colspan="1">–</td>
              <td rowspan="1" colspan="1">–</td>
              <td rowspan="1" colspan="1">–</td>
              <td rowspan="1" colspan="1">–</td>
              <td rowspan="1" colspan="1">–</td>
              <td rowspan="1" colspan="1">–</td>
              <td rowspan="1" colspan="1">&gt;99.99</td>
              <td rowspan="1" colspan="1">0.01(Fe+P+O<sub>2</sub>)</td>
            </tr>
          </tbody>
        </table>
      </table-wrap>
      <fig id="F2" position="float" orientation="portrait">
        <object-id content-type="doi">10.3897/nucet.10.129596.figure2</object-id>
        <object-id content-type="arpha">813BD00F-53D8-52BB-98F5-205BA6D8A1C1</object-id>
        <label>Figure 2.</label>
        <caption>
          <p>Schematic setup of wetting and interaction experiments.</p>
        </caption>
        <graphic xlink:href="nucet-10-e129596-g002.jpg" position="float" orientation="portrait" xlink:type="simple" id="oo_1121825.jpg">
          <uri content-type="original_file">https://binary.pensoft.net/fig/1121825</uri>
        </graphic>
      </fig>
      <p>This study investigated the interaction of pure Fe, AISI 420, EK-181, and 316L steels with a pure tungsten substrate. The convenient sessile drop method was used in first stage of experiments. The steel and iron with a volume of approximately 64 mm<sup>3</sup> were placed on 20×20×2 mm tungsten plates. The tungsten substrates were ground with sandpaper (120–2500) and polished with diamond paste (3 and 1 µm) prior to the experiments. Both steel and tungsten were cleaned in alcohol in an ultrasonic bath to remove surface pollution that could affect the liquid-solid interaction.</p>
      <p>The specimens were heated to the exposure temperature (T<sub>EX</sub>) in a vacuum resistance furnace with a heating rate of about 18 °C/min. The heating modes and material properties are listed in Table <xref ref-type="table" rid="T2">2</xref>. The exposure time was set at 1 and 10 minutes, and the vacuum level was maintained lower than 5×10<sup>-5</sup> Torr. Cooling with a furnace follows after exposure. The cooling rate from T<sub>EX</sub> to 1300 was approximately 100 °C/min, it decrease exponentially with a time. The wetting angle was studied after cooling to the room temperature in a furnace. The heating modes were designed to simulate the interaction of molten steel with tungsten fibers in the composite. As steel AISI 316L has the lowest melting point, it was also melted at 1500 °C. In this case exposure was excluded to simulate short-term interaction conditions. The temperature measurement error was about ±10 °C.</p>
      <table-wrap id="T2" position="float" orientation="portrait">
        <label>Table 2.</label>
        <caption>
          <p>Heating modes and material properties</p>
        </caption>
        <table id="TID0EHIBG" rules="all">
          <tbody>
            <tr>
              <th rowspan="1" colspan="1">Material</th>
              <th rowspan="1" colspan="1">Solidus (T<sub>S</sub>), °C</th>
              <th rowspan="1" colspan="1">Liquidus (T<sub>L</sub>), °C</th>
              <th rowspan="1" colspan="1">Exposure temperature (T<sub>EX</sub>), °C</th>
            </tr>
            <tr>
              <td rowspan="1" colspan="1">Fe</td>
              <td rowspan="1" colspan="2">1539</td>
              <td rowspan="1" colspan="1">1550, 1600</td>
            </tr>
            <tr>
              <td rowspan="1" colspan="1">AISI 420</td>
              <td rowspan="1" colspan="1">1450</td>
              <td rowspan="1" colspan="1">1510</td>
              <td rowspan="1" colspan="1">1550, 1600</td>
            </tr>
            <tr>
              <td rowspan="1" colspan="1">EK-181</td>
              <td rowspan="1" colspan="1">1503</td>
              <td rowspan="1" colspan="1">1513</td>
              <td rowspan="1" colspan="1">1550, 1600</td>
            </tr>
            <tr>
              <td rowspan="1" colspan="1">AISI316L</td>
              <td rowspan="1" colspan="1">1375</td>
              <td rowspan="1" colspan="1">1400</td>
              <td rowspan="1" colspan="1">1500, 1550, 1600</td>
            </tr>
          </tbody>
        </table>
      </table-wrap>
      <p>The second stage was dedicated to the study of microstructure and phase formation during high-temperature interaction. Steel, iron, and tungsten were cut into 5×5×3 mm pieces, and the heating conditions were the same as in stage 1. Specimens of molten steel on tungsten were prepared according to the conventional method for studying microstructures. The specimens were named as follows: “WSteel/exposure temperature/exposure time”, for example: W316/1500/1. The microstructure was examined via Scanning Electron Microscopy (<abbrev xlink:title="Scanning Electron Microscopy" id="ABBRID0EEBAE">SEM</abbrev>) using the JEOL JSM–6610LV. Qualitative elemental analysis was performed using Energy Dispersive Spectrometry (<abbrev xlink:title="Energy Dispersive Spectrometry" id="ABBRID0EIBAE">EDS</abbrev>) on the Oxford Instruments INCA x-act.</p>
      <p>The phase composition was analyzed using X-ray diffraction (<abbrev xlink:title="X-ray diffraction" id="ABBRID0EOBAE">XRD</abbrev>) on a Brucker D8 Discover. Detecting small components of the structure was challenging due to technical limitations. To increase the accuracy of phase identification the local transient synchrotron <abbrev xlink:title="X-ray diffraction" id="ABBRID0ESBAE">XRD</abbrev> with a wavelength of 0.75 Å was used. Thermodynamic calculations were performed using Thermo-Calc software with the TCFE10 database. The phase composition at room temperature was calculated based on the local chemical analysis of specimens melted at 1550 °C.</p>
    </sec>
    <sec sec-type="﻿Results and discussion" id="SECID0EWBAE">
      <title>﻿Results and discussion</title>
      <sec sec-type="﻿Wetting of tungsten substrate by steels and iron" id="SECID0E1BAE">
        <title>﻿Wetting of tungsten substrate by steels and iron</title>
        <p>To measure the wetting characteristics, the specimens were heated to the T<sub>EX</sub> above their melting point. Exposure for 1 and 10 minutes ensured complete melting of the steel and iron. After cooling, each tungsten plate was completely wetted by the steel and iron, as the liquid metal wet the front and back sides of the tungsten plate. Consequently, there was no way to measure the contact angle, as it equaled zero. The results of the wetting experiments are illustrated in the photo in Fig. <xref ref-type="fig" rid="F4">3</xref>.</p>
        <fig id="F4" position="float" orientation="portrait">
          <object-id content-type="doi">10.3897/nucet.10.129596.figure3</object-id>
          <object-id content-type="arpha">2A60A7BD-BEB0-5926-B1DC-76D9CD4889DA</object-id>
          <label>Figure 3.</label>
          <caption>
            <p>Tungsten plate before wetting and after wetting by iron at 1550 °C.</p>
          </caption>
          <graphic xlink:href="nucet-10-e129596-g004.jpg" position="float" orientation="portrait" xlink:type="simple" id="oo_1121826.jpg">
            <uri content-type="original_file">https://binary.pensoft.net/fig/1121826</uri>
          </graphic>
        </fig>
        <fig id="F3" position="float" orientation="portrait">
          <object-id content-type="doi">10.3897/nucet.10.129596.figure4</object-id>
          <object-id content-type="arpha">8825D3C6-7BC0-52EF-94B2-939202271B08</object-id>
          <label>Figure 4.</label>
          <caption>
            <p>Calculated Fe-W phase diagram (<xref ref-type="bibr" rid="B16">Jacob et al. 2015</xref>).</p>
          </caption>
          <graphic xlink:href="nucet-10-e129596-g003.jpg" position="float" orientation="portrait" xlink:type="simple" id="oo_1121827.jpg">
            <uri content-type="original_file">https://binary.pensoft.net/fig/1121827</uri>
          </graphic>
        </fig>
        <p>Long exposure times at T<sub>EX</sub> significantly higher than T<sub>L</sub>, followed by cooling and crystallization, may affect the results. At a temperature of 1500 °C, steel 316L was overheated by 100 °C above the liquidus temperature. The total time in liquid state is the sum of heating time (4 min for heating from T<sub>L</sub> to 1500), exposure time (1 min) and cooling time (~1 min), which gives us 7 min.</p>
        <p>The iron has a fixed melting point while steels melt in a certain temperature interval. The exposure temperature of 1550 °C is 11 °C higher than the melting point of pure iron. In this case, the total time in the liquid state was 2 minutes. The differences in chemical composition, melting points, and exposure times between the two considered cases do not affect the wetting process. It can be concluded that Fe-based materials wet tungsten well at a temperature range of steel and iron melting point. This characteristic is advantageous for utilizing capillary forces to form a composite structure.</p>
      </sec>
      <sec sec-type="﻿Features of interaction between tungsten and steel melt" id="SECID0EMDAE">
        <title>﻿Features of interaction between tungsten and steel melt</title>
        <sec sec-type="﻿Interaction between W and Fe" id="SECID0EQDAE">
          <title>﻿<italic>Interaction between W and Fe</italic></title>
          <p>The phase composition and structure of the joint significantly impact the final properties of the composite material. The formation of brittle phases during high-temperature interaction is critical for the mechanical properties of the composite. Iron forms two IMCs with tungsten: µ (Fe<sub>7</sub>W<sub>6</sub>) and Laves λ (Fe<sub>2</sub>W). These phases are expected to form when liquid steel fills the capillaries in the tungsten mesh. A binary Fe-W phase diagram is presented in Fig. <xref ref-type="fig" rid="F3">4</xref>.</p>
          <p>To characterize the relationship between the steel chemical composition and the tungsten-steel joint structure, iron and various steels were melted on a tungsten substrate according to the modes from the wetting experiment. The interaction between iron and tungsten represents the simplest case, thus we will begin the discussion with it. Furthermore, the simple Fe-W composition allows for the determination of the phase composition via the binary phase diagram.</p>
          <p>Microstructure images of <abbrev xlink:title="Scanning Electron Microscopy" id="ABBRID0EFEAE">SEM</abbrev> of iron melted on tungsten at 1550 °C are shown in Fig. <xref ref-type="fig" rid="F5">5</xref>. Due to the high number of microstructure images, only a few of them are showed in this paper. An interlayer with the typical for as-cast metal dendrite structure covers the tungsten surface. Within iron-based matrix <abbrev xlink:title="intermetallic compounds" id="ABBRID0ENEAE">IMC</abbrev> form dendrite structure with various shapes and sizes. As the temperature increases, the dendrite structure in matrix and <abbrev xlink:title="intermetallic compounds" id="ABBRID0EREAE">IMC</abbrev> interlayer becomes thicker. Cracks are distinctly visible at the interface between the tungsten and the interlayer, with some cracks propagating from the outer surface to the interlayer.</p>
          <fig id="F5" position="float" orientation="portrait">
            <object-id content-type="doi">10.3897/nucet.10.129596.figure5</object-id>
            <object-id content-type="arpha">90330667-199F-5C04-BDEE-D8F72F03CD00</object-id>
            <label>Figure 5.</label>
            <caption>
              <p>Microstructure of WFe/1550/10.</p>
            </caption>
            <graphic xlink:href="nucet-10-e129596-g005.jpg" position="float" orientation="portrait" xlink:type="simple" id="oo_1121828.jpg">
              <uri content-type="original_file">https://binary.pensoft.net/fig/1121828</uri>
            </graphic>
          </fig>
          <p>The chemical composition of the interlayer measured with <abbrev xlink:title="Energy Dispersive Spectrometry" id="ABBRID0EDFAE">EDS</abbrev> analysis was studied on the WFe/1550/10 specimen. Point 1 with a composition of 57.3Fe-42.7W at.% is expected to be µ-phase. It should be noted that the µ-phase deviate from stoichiometric composition at the room temperature, which is typical for casted metals The chemical composition of µ-phase corresponds to the equilibrium composition at 800 °C. Point 2 with a composition of 93.9Fe-6.1W at.% corresponds to the iron matrix around µ-phase The chemical compositions of points 1 and 2 are marked on the Fe-W phase diagram in Fig. <xref ref-type="fig" rid="F3">4</xref>. Light grey phases in the iron matrix have a composition close to the Point 1.</p>
          <p>The <abbrev xlink:title="Energy Dispersive Spectrometry" id="ABBRID0ENFAE">EDS</abbrev> map of specimens obtained after the long-term exposure at 1600 °C is shown in Fig. <xref ref-type="fig" rid="F6">6</xref>. It is apparent that Fe does not significantly diffuse into the base W, while tungsten actively dissolves in iron. The high W content at different distances from the joint indicates that diffusion primarily occurs in the liquid state.</p>
          <fig id="F6" position="float" orientation="portrait">
            <object-id content-type="doi">10.3897/nucet.10.129596.figure6</object-id>
            <object-id content-type="arpha">88A852F5-EB1C-5D59-8F43-4A64A1B55F7B</object-id>
            <label>Figure 6.</label>
            <caption>
              <p>Microstructure and <abbrev xlink:title="Energy Dispersive Spectrometry" id="ABBRID0E4FAE">EDS</abbrev> map of WFe/1600/10 specimen.</p>
            </caption>
            <graphic xlink:href="nucet-10-e129596-g006.jpg" position="float" orientation="portrait" xlink:type="simple" id="oo_1121829.jpg">
              <uri content-type="original_file">https://binary.pensoft.net/fig/1121829</uri>
            </graphic>
          </fig>
          <p>Due to the extremely low solubility of W in Fe at the room temperature, the equilibrium state consists of α-Fe and the µ-phase. <abbrev xlink:title="Scanning Electron Microscopy" id="ABBRID0EIGAE">SEM</abbrev> analysis did not reveal the λ phase, which is stable in the temperature range of 150–1100 °C. This phase is expected to form during decomposition of µ and α-Fe due to diffusion in solid state. All phases observed near the joint area exhibit a similar composition close to the µ-phase. The chemical composition of the iron matrix becomes enriched with tungsten content with increasing exposure temperature, indicating that overheated liquid iron actively dissolves tungsten. The matrix of specimens melted at 1550 °C contains 4.3 at.% of W, whereas at 1600 °C it contains 6.3 at.%.</p>
          <p>The absence of the Laves λ-phase and the non-equilibrium composition of phases could indicate that cooling suppresses the phase evolution in the steel matrix. When solidification under equilibrium conditions occurs, the matrix should undergo a series of phase transformations: L→α-Fe+µ→α-Fe+λ→α-Fe+µ. At the room temperature, the α-Fe+µ composition is stable.</p>
        </sec>
        <sec sec-type="﻿Interaction between AISI 420, EK-181 and W" id="SECID0ENGAE">
          <title>﻿<italic>Interaction between AISI 420, EK-181 and W</italic></title>
          <p>The <abbrev xlink:title="Reduced Activation Ferritic-Martensitic" id="ABBRID0EVGAE">RAFM</abbrev> steel EK-181 does not significantly differ from AISI 420 in chemical composition. The influence of micro-alloying on wetting and interaction is considered negligible. Therefore, main features will be discussed based on the AISI 420 case.</p>
          <p>The investigation aims to determine the influence of the steel alloying elements on the structure of the interlayer. AISI 420, characterized by high chromium and carbon content, was melted on a tungsten substrate at 1550 and 1600 °C. The microstructure image of the W420/1600/10 specimen and <abbrev xlink:title="Energy Dispersive Spectrometry" id="ABBRID0E2GAE">EDS</abbrev> maps are presented in Fig. <xref ref-type="fig" rid="F7">7</xref>, revealing a similar dendrite structure. An <abbrev xlink:title="intermetallic compounds" id="ABBRID0EDHAE">IMC</abbrev> layer covers the entire surface of tungsten. Notably, no cracks or pores were observed in the W420 joints, in contrast to the WFe case. The modified µ-phase at point 1 with composition of 4Cr-53.3Fe-42.7W at.% contains chromium. Point 2 in the steel matrix with composition of 5.8Cr-89.5Fe-4.7W at.% contains a lower tungsten content than in the case of WFe melted in the same way.</p>
          <fig id="F7" position="float" orientation="portrait">
            <object-id content-type="doi">10.3897/nucet.10.129596.figure7</object-id>
            <object-id content-type="arpha">EFA0E153-AADA-5842-B799-EAB2BFC5DE70</object-id>
            <label>Figure 7.</label>
            <caption>
              <p>Microstructure of W420/1600/10 specimen.</p>
            </caption>
            <graphic xlink:href="nucet-10-e129596-g007.jpg" position="float" orientation="portrait" xlink:type="simple" id="oo_1121830.jpg">
              <uri content-type="original_file">https://binary.pensoft.net/fig/1121830</uri>
            </graphic>
          </fig>
          <p>Chromium actively diffuses into the tungsten substrate. Chromium has high solubility in tungsten especially at high temperatures. This is verified by comparing the Cr content in the matrix between melting at 1550 and 1600 °C. Chromium content is 7.8 at.% in the specimens melted at 1550 while melting at 1600 results in the decrease of chromium content down to 5.8 at.%.</p>
          <p>The carbon content of 420 steel is the highest among the studied steels. However, detecting carbon with high accuracy is challenging due to its low mass and surface pollution. We assume that carbon affects phase formation primarily due to its high affinity for tungsten. The affinity of W to C is reported to be higher than that of Cr (<xref ref-type="bibr" rid="B17">Jansson and Lewin 2013</xref>). While <abbrev xlink:title="X-ray diffraction" id="ABBRID0E1HAE">XRD</abbrev> is a common method for determining phase composition, it can be challenging to detect microscopic precipitates using this technique. The peaks observed correspond to α-Fe solid solution, Fe<sub>7</sub>W<sub>6</sub>, Fe<sub>2</sub>W, and Fe oxides detected in the <abbrev xlink:title="X-ray diffraction" id="ABBRID0EEIAE">XRD</abbrev> spectra measured across the entire specimen, including the interlayer and steel matrix zone. Consequently, the phase composition of each individual zone in the joint remains unclear.</p>
          <p>To estimate the probable phase composition, thermodynamic calculations were carried out using Thermo-Calc software. Phase composition of tungsten-steel joint zone studied via synchrotron <abbrev xlink:title="X-ray diffraction" id="ABBRID0EKIAE">XRD</abbrev> technique. Due to high specimens number only one spectra presented in Fig. <xref ref-type="fig" rid="F8">8</xref>. The results of phase composition calculation of two points presented in Table <xref ref-type="table" rid="T3">3</xref>. Point 1 (Fe-41.5W-5.3Cr-1C at.%) and 2 (Fe-4.5W-7.8C-1C at.%) corresponds to chemical composition of <abbrev xlink:title="intermetallic compounds" id="ABBRID0EWIAE">IMC</abbrev> layer and steel matrix respectively. Initial AISI 420 steel contain approximately 1 at.% of carbon. Therefore, all chemical compositions in Thermocalc thermodynamic calculations are alloyed with 1 at.% carbon to evaluate the effect of carbon.</p>
          <table-wrap id="T3" position="float" orientation="portrait">
            <label>Table 3.</label>
            <caption>
              <p>Phase composition modeling of W420 joint alloyed with carbon</p>
            </caption>
            <table id="TID0EFPBG" rules="all">
              <tbody>
                <tr>
                  <th rowspan="1" colspan="1">Phase name</th>
                  <th rowspan="1" colspan="1">Chemical composition, at.%</th>
                  <th rowspan="1" colspan="1">Equilibrium composition</th>
                  <th rowspan="1" colspan="1">Experimental data from <abbrev xlink:title="X-ray diffraction" id="ABBRID0EUJAE">XRD</abbrev></th>
                </tr>
                <tr>
                  <td rowspan="1" colspan="1"><abbrev xlink:title="intermetallic compounds" id="ABBRID0E3JAE">IMC</abbrev> layer</td>
                  <td rowspan="1" colspan="1">Fe-41.5W-5.3Cr-1C</td>
                  <td rowspan="1" colspan="1">µ-phase, λ-phase, M<sub>6</sub>C</td>
                  <td rowspan="1" colspan="1">α-Fe, µ-phase, λ-phase (traces)</td>
                </tr>
                <tr>
                  <td rowspan="1" colspan="1">Steel matrix</td>
                  <td rowspan="1" colspan="1">Fe-4.5W-7.8C-1C</td>
                  <td rowspan="1" colspan="1">α-Fe, λ-phase, M<sub>23</sub>C<sub>6</sub></td>
                  <td rowspan="1" colspan="1"/>
                </tr>
              </tbody>
            </table>
          </table-wrap>
          <fig id="F8" position="float" orientation="portrait">
            <object-id content-type="doi">10.3897/nucet.10.129596.figure8</object-id>
            <object-id content-type="arpha">DD444C92-B0E9-5187-AFB4-C342F2BFF28A</object-id>
            <label>Figure 8.</label>
            <caption>
              <p>Example of <abbrev xlink:title="X-ray diffraction" id="ABBRID0EFLAE">XRD</abbrev> spectra of WFe/1550/10 specimen.</p>
            </caption>
            <graphic xlink:href="nucet-10-e129596-g008.jpg" position="float" orientation="portrait" xlink:type="simple" id="oo_1121831.jpg">
              <uri content-type="original_file">https://binary.pensoft.net/fig/1121831</uri>
            </graphic>
          </fig>
          <p>The calculations show that M<sub>6</sub>C carbide forms due to the high W-C affinity and remains stable in a broad temperature range. In the high-temperature range, the phase composition primarily consists of the µ-phase. Within the matrix composition, carbon form M<sub>6</sub>C and M<sub>23</sub>C<sub>6</sub> type carbide phases. The primary component of the matrix is the α-Fe solid solution. Tungsten and chromium are both strong carbide formers, the absence of Cr and W carbides in the structure indicates that the dissolved carbon or carbides in the matrix are too small to detect. Calculated compositions suggest that the Laves λ-phase is thermodynamically stable at lower temperatures.</p>
          <p>Comparison of the <abbrev xlink:title="X-ray diffraction" id="ABBRID0E1LAE">XRD</abbrev> results and calculations leads to the conclusion that the W420 joint consists of µ-phase, α-Fe matrix, and Laves λ-phase. The absence of carbides in the <abbrev xlink:title="X-ray diffraction" id="ABBRID0E5LAE">XRD</abbrev> analysis is attributed to their small size and technical constraints. Traces of the Laves phase indicate that its content and size are insufficient for reliable analysis. In comparison with data obtained by casting steel at 1550 °C in (<xref ref-type="bibr" rid="B19">Kumar 2013</xref>) we can conclude that Laves λ-phase does not play significant role in intermetallic layer structure. Due to lower W content in λ-phase they most likely to form in steel matrix away from W wire.</p>
        </sec>
        <sec sec-type="﻿Interaction between W and AISI 316L" id="SECID0EGMAE">
          <title>﻿<italic>Interaction between W and AISI 316L</italic></title>
          <p>The second steel type contains Ni and Cr, while the carbon content is low. Steel 316L also has a low melting point, allowing us to utilize an additional mode without exposure at 1500 °C (immediate cooling after rapid heating). However, no difference in microstructure was observed between specimens with and without 1-minute exposure. The microstructure of steel 316L melted on tungsten at 1500 and 1600 °C for 0 and 10 minutes, respectively, is shown in Fig. <xref ref-type="fig" rid="F9">9</xref>.</p>
          <fig id="F9" position="float" orientation="portrait">
            <object-id content-type="doi">10.3897/nucet.10.129596.figure9</object-id>
            <object-id content-type="arpha">9A05DD09-C779-53E6-AA38-B4BF244A0DAA</object-id>
            <label>Figure 9.</label>
            <caption>
              <p>Microstructure of W316/1500/0 and W316/1600/1 specimens.</p>
            </caption>
            <graphic xlink:href="nucet-10-e129596-g009.jpg" position="float" orientation="portrait" xlink:type="simple" id="oo_1121832.jpg">
              <uri content-type="original_file">https://binary.pensoft.net/fig/1121832</uri>
            </graphic>
          </fig>
          <p>High-temperature exposure with overheating by 150 °C (W316/1550 specimen) above the melting point results in significant erosion of tungsten grains by the liquid metal. A W cluster exceeding 50 µm in size was detected in the steel matrix. Further away from the joint zone, a fine grid structure was observed. Conversely, overheating by approximately 100 °C above the melting temperatures only leads to the growth of the dendritic structure.</p>
          <p>The thickness of the intermediate joint layer at 1500 °C is about 5 µm. Point 1 (marked in Fig. <xref ref-type="fig" rid="F9">9a</xref>) has composition of 12.3Cr-45.3Fe-3.9Ni-38.5W at.%, which is presumed to be a modified µ-phase. Nickel was not detected deep in the bulk tungsten, while chromium actively diffuses at all studied temperatures. Point 2 corresponds to a steel matrix with composition of 16.3Cr-68.2Fe-11.2Ni-4.3W at.%. Matrix has a high tungsten content; the content of other elements remains at the same level.</p>
          <p>The maps of chemical elements distribution shown in Fig. <xref ref-type="fig" rid="F10">10</xref> illustrate the erosion process in the case of the W316/1600/10 sample, where liquid steel actively dissolves the tungsten grain boundaries. Point 1 in Fig. <xref ref-type="fig" rid="F9">9b</xref> has a composition of 3.5Cr-48.9Fe-5.1Ni-42.5W at.%. It is evident that the Cr content is significantly lower in the µ-phase, while Ni content has increased compared to the W316/1500/0. The steel matrix at point 2 has a low Cr content of about 4.5 at.%. A fine grid of Cr-based phases is observed in both the <abbrev xlink:title="Energy Dispersive Spectrometry" id="ABBRID0EPNAE">EDS</abbrev> maps and the <abbrev xlink:title="Scanning Electron Microscopy" id="ABBRID0ETNAE">SEM</abbrev> image.</p>
          <fig id="F10" position="float" orientation="portrait">
            <object-id content-type="doi">10.3897/nucet.10.129596.figure10</object-id>
            <object-id content-type="arpha">4406317C-91F4-5D63-B5F2-E33DEABE60AC</object-id>
            <label>Figure 10.</label>
            <caption>
              <p><abbrev xlink:title="Energy Dispersive Spectrometry" id="ABBRID0E6NAE">EDS</abbrev> map of W316/1600/10 specimen.</p>
            </caption>
            <graphic xlink:href="nucet-10-e129596-g010.jpg" position="float" orientation="portrait" xlink:type="simple" id="oo_1121833.jpg">
              <uri content-type="original_file">https://binary.pensoft.net/fig/1121833</uri>
            </graphic>
          </fig>
          <p>The phase composition of W316 specimens studied in the same way as W420. For thermodynamic calculations two compositions were used: Fe-41W-7Cr-4Ni at.% (<abbrev xlink:title="intermetallic compounds" id="ABBRID0EKOAE">IMC</abbrev> layer) and Fe-5W-9Cr-13Ni at.% (steel matrix). Calculations presented in Table <xref ref-type="table" rid="T4">4</xref> show that the equilibrium composition for steel matrix is a mixture of γ-Fe and α-Fe solid solutions with λ-phase, while <abbrev xlink:title="intermetallic compounds" id="ABBRID0ESOAE">IMC</abbrev> layer has composition of µ-phase, λ-phase with some γ-Fe additions. The <abbrev xlink:title="X-ray diffraction" id="ABBRID0EWOAE">XRD</abbrev> results shows clear peaks of γ-Fe and µ-phase, while α-Fe and λ-phase remain undetected.</p>
          <table-wrap id="T4" position="float" orientation="portrait">
            <label>Table 4.</label>
            <caption>
              <p>Phase composition modeling of W316 joint alloyed with carbon</p>
            </caption>
            <table id="TID0EKTBG" rules="all">
              <tbody>
                <tr>
                  <th rowspan="1" colspan="1">Phase name</th>
                  <th rowspan="1" colspan="1">Chemical composition, at.%</th>
                  <th rowspan="1" colspan="1">Equilibrium composition</th>
                  <th rowspan="1" colspan="1">Experimental data from <abbrev xlink:title="X-ray diffraction" id="ABBRID0EUPAE">XRD</abbrev></th>
                </tr>
                <tr>
                  <td rowspan="1" colspan="1"><abbrev xlink:title="intermetallic compounds" id="ABBRID0E3PAE">IMC</abbrev> layer</td>
                  <td rowspan="1" colspan="1">Fe-41W-7Cr-4Ni</td>
                  <td rowspan="1" colspan="1">µ-phase, λ-phase, γ-Fe</td>
                  <td rowspan="1" colspan="1">γ-Fe, µ-phase</td>
                </tr>
                <tr>
                  <td rowspan="1" colspan="1">Steel matrix</td>
                  <td rowspan="1" colspan="1">Fe-5W-9Cr-13Ni</td>
                  <td rowspan="1" colspan="1">α-Fe, γ-Fe, λ-phase</td>
                  <td rowspan="1" colspan="1"/>
                </tr>
              </tbody>
            </table>
          </table-wrap>
        </sec>
        <sec sec-type="﻿Phase evolution" id="SECID0EWQAE">
          <title>﻿<italic>Phase evolution</italic></title>
          <p>The microstructure evolution stages are presented in a schematic representation in Fig. <xref ref-type="fig" rid="F11">11</xref>. Two types of interaction with the melt have been established: diffusion and erosion. Both steels AISI 420, EK-181 and iron exhibit similar behaviors when interacting with tungsten, resulting in the formation of a dendritic structure with varying thickness in the interaction zone. A layer of µ-phase <abbrev xlink:title="intermetallic compounds" id="ABBRID0ECRAE">IMC</abbrev> composed of Fe, W, and Cr covers the surface of tungsten.</p>
          <fig id="F11" position="float" orientation="portrait">
            <object-id content-type="doi">10.3897/nucet.10.129596.figure11</object-id>
            <object-id content-type="arpha">401A4E53-29A8-5517-A50A-913553F1E864</object-id>
            <label>Figure 11.</label>
            <caption>
              <p>Schematic illustration of liquid melt interaction with W.</p>
            </caption>
            <graphic xlink:href="nucet-10-e129596-g011.jpg" position="float" orientation="portrait" xlink:type="simple" id="oo_1121834.jpg">
              <uri content-type="original_file">https://binary.pensoft.net/fig/1121834</uri>
            </graphic>
          </fig>
          <p><abbrev xlink:title="intermetallic compounds" id="ABBRID0EURAE">IMC</abbrev> layer is formed during interaction of the melt with solid tungsten due to relatively slow diffusion process on the solid/liquid boundary The liquid near the boundary becomes enriched with W, which raises the melting point, leading to nucleation of a µ-phase on the surface of tungsten. The W-Fe diagram shown in Fig. <xref ref-type="fig" rid="F12">12</xref> can be used to define the composition of liquid and solid structure. In this stage liquid near W form diffusion layer with composition close to C<sub>L</sub> point in Fig. <xref ref-type="fig" rid="F12">12</xref>. When W content increase due to diffusion, the solid µ-phase nucleate. <abbrev xlink:title="intermetallic compounds" id="ABBRID0ECSAE">IMC</abbrev> start to grow in form of dendrites forming solidification front. The chemical composition of µ-phase corresponds to C<sub>s</sub> point in diagram. Diffusion layer quickly propagates due to high diffusion rate in liquid state. Described process undergo until cooling starts.</p>
          <fig id="F12" position="float" orientation="portrait">
            <object-id content-type="doi">10.3897/nucet.10.129596.figure12</object-id>
            <object-id content-type="arpha">05E4DA56-F5D7-5304-83F5-69C396AD7BB9</object-id>
            <label>Figure 12.</label>
            <caption>
              <p>Fe corner of W-Fe diagram.</p>
            </caption>
            <graphic xlink:href="nucet-10-e129596-g012.jpg" position="float" orientation="portrait" xlink:type="simple" id="oo_1121835.jpg">
              <uri content-type="original_file">https://binary.pensoft.net/fig/1121835</uri>
            </graphic>
          </fig>
          <p>Cooling cause fast temperature drop. Thus, C<sub>L</sub> point shifts to C’<sub>S</sub> which means that liquid crystallize in form of α-Fe enriched with W. After that follows decomposition with µ-phase grow in α-Fe. The composition of α-Fe change according solvus from point C’<sub>S</sub> to C”<sub>S</sub>. The <abbrev xlink:title="Energy Dispersive Spectrometry" id="ABBRID0E5SAE">EDS</abbrev> data evidence that ~5 at.% of W remains in steel, which means that diffusion after 1100 °C is weak. The composition of µ-phase remains close to C<sub>s</sub> due to the fact that it is stable composition for wide range of temperatures.</p>
          <p>When overheating exceeds 150 degrees (W316 specimens melted at 1500 and 1600 °C) selective dissolution of grain boundaries occur. This feature illustrated in Fig. <xref ref-type="fig" rid="F13">13</xref>. The liquid melt separates single grain, absorbs it and dissolves it. This process, previously observed in studies of corrosion of refractory alloys (<xref ref-type="bibr" rid="B23">Lyutyi et al. 1991</xref>), is associated with the grain boundaries energy and impurities in them.</p>
          <fig id="F13" position="float" orientation="portrait">
            <object-id content-type="doi">10.3897/nucet.10.129596.figure13</object-id>
            <object-id content-type="arpha">2A512519-7BC6-59C0-95CE-813AD77E845A</object-id>
            <label>Figure 13.</label>
            <caption>
              <p>Tungsten grain boundary erosion by liquid AISI 316L melt.</p>
            </caption>
            <graphic xlink:href="nucet-10-e129596-g013.jpg" position="float" orientation="portrait" xlink:type="simple" id="oo_1121836.jpg">
              <uri content-type="original_file">https://binary.pensoft.net/fig/1121836</uri>
            </graphic>
          </fig>
          <p>Cooling down at a relatively high rate follows the exposure. When cooling under furnace conditions, the temperature drops from 1550–1600 to 1300 °C at an approximate rate of 100 °C/min. As a result, solidification occurs immediately after the exposure ends. The liquid steel, enriched with tungsten, solidifies as an α-Fe solid solution of non-equilibrium composition.</p>
          <p>After solidification, diffusion rate significantly drops, resulting in minimal changes in the distribution of chemical elements. The stage of solid phase decomposition is characterized by a low cooling rate, which decreases exponentially over time. Consequently, phase decomposition occurs partially. During decomposition, a secondary µ-phase nucleates in the steel matrix. According to <abbrev xlink:title="X-ray diffraction" id="ABBRID0E4TAE">XRD</abbrev> λ-phase precipitates only in the W420 joint.</p>
        </sec>
        <sec sec-type="﻿Results application and future work" id="SECID0EBUAE">
          <title>﻿<italic>Results application and future work</italic></title>
          <p>The results obtained demonstrate that iron and steel perfectly wet the tungsten surface. The capillary forces are strong enough to wet not only the polished face but also the back side of the tungsten plate. In this experiment, tungsten and steel were heated to the same temperature. Under these isothermal conditions, wetting occurs simultaneously. However, in real liquid metal injection technology, the tungsten mesh might have a lower temperature than the liquid steel, which would prevent undesirable interaction and lead to obtaining an optimal structure.</p>
          <p>To achieve this, several issues need to be considered. The first is the interaction of melted steel with tungsten at a lower temperature. This can be addressed by injecting melted steel onto a tungsten substrate, heated separately to a different temperature. Sessile drop method allow to measure wetting angle of steel melt at various substrates heated to lower temperature (<xref ref-type="bibr" rid="B21">Long et al. 2024</xref>).</p>
          <p>The second issue to consider is the use of barrier layers, which might completely prevent the interaction. A layer such as tungsten carbide (WC, W<sub>2</sub>C, α-WC<sub>1-x</sub>) appears to meet wetting, CTE and thermal conductivity requirements (<xref ref-type="bibr" rid="B29">Reeber and Wang 1999</xref>; <xref ref-type="bibr" rid="B40">Zhou et al. 2003</xref>; <xref ref-type="bibr" rid="B35">Tripathy et al. 2022</xref>). Thermodynamic calculations show that M<sub>6</sub>C carbide is formed at high carbon content and is thermodynamically stable until the steel is melted. If the carbide layer is thin enough, the effect on thermal conductivity is negligible. Oxide and nitride ceramics are strictly prohibited due to their interaction with Li under tokamak conditions. Corrosion resistance in liquid metal environment comes from the expected conditions of tokamak with reactor technologies (<xref ref-type="bibr" rid="B24">Mazul et al. 2021</xref>).</p>
          <p>The actual structure of tungsten mesh infiltrated with steel melt depend on the mesh size, thickness and temperature of W wire, temperature of steel melt. During infiltration the steel melt temperature will inevitably decrease to solidus. Intermetallic layer on W wire could block capillaries between wires if the rate of <abbrev xlink:title="intermetallic compounds" id="ABBRID0EIVAE">IMC</abbrev> grow is higher than the rate of colling.</p>
        </sec>
      </sec>
    </sec>
    <sec sec-type="﻿Conclusion" id="SECID0EMVAE">
      <title>﻿Conclusion</title>
      <p>The investigation focuses on the wetting characteristics and joint structure of tungsten with iron, EK-181, AISI 420, and 316L steels under isothermal conditions. High-temperature wetting at 1500–1600 °C reveals that all the studied materials perfectly wet the W substrate. The interaction between the melt and solid tungsten leads to the formation of a dendritic structure with a µ-phase at the solid/liquid boundary. The melt solidifies in the form of a solid solution enriched with tungsten, resulting in decomposition with the nucleation of µ and λ-phases in the iron and AISI 420 steel matrices. For the 316L steel, γ-Fe, µ-phase and α-Fe are formed.</p>
      <p>The interaction rate primarily depends on overheating of melt. The 150 °C of overheating appears to be critical point, when erosion type of interaction overcomes the diffusion type. The results show that undesired interaction might be completely suppressed by diffusion barrier layers.</p>
    </sec>
    <sec sec-type="﻿Funding" id="SECID0ESVAE">
      <title>﻿Funding</title>
      <p>This work has been supported by the grants the Russian Science Foundation, RSF 24-2300111</p>
      <p>Sample characterization using the Synchrotron was done with the support of the Ministry of Science and Higher Education of the Russian Federation (Agreement No. 075-15-2021-1352).</p>
    </sec>
  </body>
  <back>
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