Correlation between thermal, kinetic, magnetic and electric effects in the crystallization process of amorphous magnetic alloys
By use of differential scanning calorimetry the mechanism of crystallization (devitrification) was investigated for magnetic amorphous alloys of compositions Fe 82B 13Si 5 (A) and Fe 75B 10Si 15 (B) in the temperature range between ambient and 600 °C. It was shown that both alloys crystallize in two...
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description | By use of differential scanning calorimetry the mechanism of crystallization (devitrification) was investigated for magnetic amorphous alloys of compositions Fe
82B
13Si
5 (A) and Fe
75B
10Si
15 (B) in the temperature range between ambient and 600 °C. It was shown that both alloys crystallize in two stages between 480° and 520 °C. The energies of activation of the process,
E
1 = 435.2
kJ/
mol and
E
2 = 909.5
kJ/
mol for alloy A were derived, with corresponding frequency factors Z
1 = 1.1×10
30 min
−1 and Z
2 = 8.1 × 10
60 min
−1, where subscripts 1 and 2 denote the first and second stage of crystallization respectively. With alloy B the corresponding figures are
E
1= 660.2
kJ/
mol,
E
2 = 870.3
kJ/
mol,
Z
1 = 4.9 × 10
45 min
−1 and
Z
2 = 7.6 × 10
58 min
1̄. The temperature dependence of the crystallization rate constants was followed with values at exo maxima of
k
1 = 1.73 min
−1 and
k
2 = 4.17 min
−1 for alloy A and
k
1 = 3.1 min
−1 and
k
2 = 6.6 min
−1 for alloy B. Parallel to the thermal and kinetic investigations, measurements of changes of the relative electric resistance and the relative magnetic permeability were followed. A clear correlation was observed between the changes in crystal structure (X-ray diffractograms) with the changes in electron and magnetic structures, particularly in the temperature range of the principal processes of alloy devitrification. The enthalpies of crystallization are rather close and are −
ΔH =128 J/g for alloy A and 125 J/g for alloy B. |
doi_str_mv | 10.1016/0254-0584(92)90228-Z |
format | Article |
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82B
13Si
5 (A) and Fe
75B
10Si
15 (B) in the temperature range between ambient and 600 °C. It was shown that both alloys crystallize in two stages between 480° and 520 °C. The energies of activation of the process,
E
1 = 435.2
kJ/
mol and
E
2 = 909.5
kJ/
mol for alloy A were derived, with corresponding frequency factors Z
1 = 1.1×10
30 min
−1 and Z
2 = 8.1 × 10
60 min
−1, where subscripts 1 and 2 denote the first and second stage of crystallization respectively. With alloy B the corresponding figures are
E
1= 660.2
kJ/
mol,
E
2 = 870.3
kJ/
mol,
Z
1 = 4.9 × 10
45 min
−1 and
Z
2 = 7.6 × 10
58 min
1&#x0304;. The temperature dependence of the crystallization rate constants was followed with values at exo maxima of
k
1 = 1.73 min
−1 and
k
2 = 4.17 min
−1 for alloy A and
k
1 = 3.1 min
−1 and
k
2 = 6.6 min
−1 for alloy B. Parallel to the thermal and kinetic investigations, measurements of changes of the relative electric resistance and the relative magnetic permeability were followed. A clear correlation was observed between the changes in crystal structure (X-ray diffractograms) with the changes in electron and magnetic structures, particularly in the temperature range of the principal processes of alloy devitrification. The enthalpies of crystallization are rather close and are −
ΔH =128 J/g for alloy A and 125 J/g for alloy B.</description><identifier>ISSN: 0254-0584</identifier><identifier>EISSN: 1879-3312</identifier><identifier>DOI: 10.1016/0254-0584(92)90228-Z</identifier><identifier>CODEN: MCHPDR</identifier><language>eng</language><publisher>LAUSANNE 1: Elsevier B.V</publisher><subject>Applied sciences ; Condensed matter: structure, mechanical and thermal properties ; Equations of state, phase equilibria, and phase transitions ; Exact sciences and technology ; Materials Science ; Materials Science, Multidisciplinary ; Metals. Metallurgy ; Physics ; Science & Technology ; Specific phase transitions ; Technology</subject><ispartof>Materials chemistry and physics, 1992-02, Vol.30 (4), p.221-227</ispartof><rights>1992</rights><rights>1992 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>true</woscitedreferencessubscribed><woscitedreferencescount>2</woscitedreferencescount><woscitedreferencesoriginalsourcerecordid>wosA1992HK29500001</woscitedreferencesoriginalsourcerecordid><citedby>FETCH-LOGICAL-c395t-bb74f5f99db9d42d38b59fe39ad902e533741f4b9da296774003438917cd3ee23</citedby><cites>FETCH-LOGICAL-c395t-bb74f5f99db9d42d38b59fe39ad902e533741f4b9da296774003438917cd3ee23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/0254-0584(92)90228-Z$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>315,781,785,3551,27197,27929,27930,46000</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=5312090$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>SUSIC, MV</creatorcontrib><creatorcontrib>MARICIC, AM</creatorcontrib><creatorcontrib>DIMITRIJEVIC, RZ</creatorcontrib><title>Correlation between thermal, kinetic, magnetic and electric effects in the crystallization process of amorphous magnetic alloys</title><title>Materials chemistry and physics</title><addtitle>MATER CHEM PHYS</addtitle><description>By use of differential scanning calorimetry the mechanism of crystallization (devitrification) was investigated for magnetic amorphous alloys of compositions Fe
82B
13Si
5 (A) and Fe
75B
10Si
15 (B) in the temperature range between ambient and 600 °C. It was shown that both alloys crystallize in two stages between 480° and 520 °C. The energies of activation of the process,
E
1 = 435.2
kJ/
mol and
E
2 = 909.5
kJ/
mol for alloy A were derived, with corresponding frequency factors Z
1 = 1.1×10
30 min
−1 and Z
2 = 8.1 × 10
60 min
−1, where subscripts 1 and 2 denote the first and second stage of crystallization respectively. With alloy B the corresponding figures are
E
1= 660.2
kJ/
mol,
E
2 = 870.3
kJ/
mol,
Z
1 = 4.9 × 10
45 min
−1 and
Z
2 = 7.6 × 10
58 min
1&#x0304;. The temperature dependence of the crystallization rate constants was followed with values at exo maxima of
k
1 = 1.73 min
−1 and
k
2 = 4.17 min
−1 for alloy A and
k
1 = 3.1 min
−1 and
k
2 = 6.6 min
−1 for alloy B. Parallel to the thermal and kinetic investigations, measurements of changes of the relative electric resistance and the relative magnetic permeability were followed. A clear correlation was observed between the changes in crystal structure (X-ray diffractograms) with the changes in electron and magnetic structures, particularly in the temperature range of the principal processes of alloy devitrification. The enthalpies of crystallization are rather close and are −
ΔH =128 J/g for alloy A and 125 J/g for alloy B.</description><subject>Applied sciences</subject><subject>Condensed matter: structure, mechanical and thermal properties</subject><subject>Equations of state, phase equilibria, and phase transitions</subject><subject>Exact sciences and technology</subject><subject>Materials Science</subject><subject>Materials Science, Multidisciplinary</subject><subject>Metals. Metallurgy</subject><subject>Physics</subject><subject>Science & Technology</subject><subject>Specific phase transitions</subject><subject>Technology</subject><issn>0254-0584</issn><issn>1879-3312</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1992</creationdate><recordtype>article</recordtype><sourceid>EZCTM</sourceid><recordid>eNqNkU-LFDEQxYMoOK5-Aw85iChua_5Ody7C0qgrLnjRy15COl1xo-nOmGRcxotf3cz0MHiSzSUV8nuPqlcIPaXkNSV0_YYwKRoiO_FCsZeKMNY11_fQinatajin7D5anZCH6FHO3wmhLaV8hf70MSUIpvg44wHKLcCMyw2kyYRz_MPPULw9x5P5dqiwmUcMAWxJ9QHO1Spjf5Bgm3a5mBD878Vuk6KFnHF02EwxbW7iNv_jFELc5cfogTMhw5PjfYa-vn_3pb9srj5_-NhfXDWWK1maYWiFk06pcVCjYCPvBqkccGXGOi9IzltBnaifhql12wpCuOCdoq0dOQDjZ-j54lub-rmFXPTks4UQzAy1Lc2krDCjdwG7dUe6CooFtCnmnMDpTfKTSTtNid6vRe8z1_vMtWL6sBZ9XWXPjv4mWxNcMrP1-aSVdV1EkYp1C3YLQ3TZepgtnKgLqhS7_MSUJPXQ3pdD4n3czqVKX91dWum3Cw01_V8ekj4qRp_qcvUY_f8H-guudsR4</recordid><startdate>19920201</startdate><enddate>19920201</enddate><creator>SUSIC, MV</creator><creator>MARICIC, AM</creator><creator>DIMITRIJEVIC, RZ</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>BLEPL</scope><scope>DTL</scope><scope>EZCTM</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>7U5</scope><scope>L7M</scope></search><sort><creationdate>19920201</creationdate><title>Correlation between thermal, kinetic, magnetic and electric effects in the crystallization process of amorphous magnetic alloys</title><author>SUSIC, MV ; MARICIC, AM ; DIMITRIJEVIC, RZ</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c395t-bb74f5f99db9d42d38b59fe39ad902e533741f4b9da296774003438917cd3ee23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1992</creationdate><topic>Applied sciences</topic><topic>Condensed matter: structure, mechanical and thermal properties</topic><topic>Equations of state, phase equilibria, and phase transitions</topic><topic>Exact sciences and technology</topic><topic>Materials Science</topic><topic>Materials Science, Multidisciplinary</topic><topic>Metals. Metallurgy</topic><topic>Physics</topic><topic>Science & Technology</topic><topic>Specific phase transitions</topic><topic>Technology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>SUSIC, MV</creatorcontrib><creatorcontrib>MARICIC, AM</creatorcontrib><creatorcontrib>DIMITRIJEVIC, RZ</creatorcontrib><collection>Web of Science Core Collection</collection><collection>Science Citation Index Expanded</collection><collection>Web of Science - Science Citation Index Expanded - 1992</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Materials chemistry and physics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>SUSIC, MV</au><au>MARICIC, AM</au><au>DIMITRIJEVIC, RZ</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Correlation between thermal, kinetic, magnetic and electric effects in the crystallization process of amorphous magnetic alloys</atitle><jtitle>Materials chemistry and physics</jtitle><stitle>MATER CHEM PHYS</stitle><date>1992-02-01</date><risdate>1992</risdate><volume>30</volume><issue>4</issue><spage>221</spage><epage>227</epage><pages>221-227</pages><issn>0254-0584</issn><eissn>1879-3312</eissn><coden>MCHPDR</coden><abstract>By use of differential scanning calorimetry the mechanism of crystallization (devitrification) was investigated for magnetic amorphous alloys of compositions Fe
82B
13Si
5 (A) and Fe
75B
10Si
15 (B) in the temperature range between ambient and 600 °C. It was shown that both alloys crystallize in two stages between 480° and 520 °C. The energies of activation of the process,
E
1 = 435.2
kJ/
mol and
E
2 = 909.5
kJ/
mol for alloy A were derived, with corresponding frequency factors Z
1 = 1.1×10
30 min
−1 and Z
2 = 8.1 × 10
60 min
−1, where subscripts 1 and 2 denote the first and second stage of crystallization respectively. With alloy B the corresponding figures are
E
1= 660.2
kJ/
mol,
E
2 = 870.3
kJ/
mol,
Z
1 = 4.9 × 10
45 min
−1 and
Z
2 = 7.6 × 10
58 min
1&#x0304;. The temperature dependence of the crystallization rate constants was followed with values at exo maxima of
k
1 = 1.73 min
−1 and
k
2 = 4.17 min
−1 for alloy A and
k
1 = 3.1 min
−1 and
k
2 = 6.6 min
−1 for alloy B. Parallel to the thermal and kinetic investigations, measurements of changes of the relative electric resistance and the relative magnetic permeability were followed. A clear correlation was observed between the changes in crystal structure (X-ray diffractograms) with the changes in electron and magnetic structures, particularly in the temperature range of the principal processes of alloy devitrification. The enthalpies of crystallization are rather close and are −
ΔH =128 J/g for alloy A and 125 J/g for alloy B.</abstract><cop>LAUSANNE 1</cop><pub>Elsevier B.V</pub><doi>10.1016/0254-0584(92)90228-Z</doi><tpages>7</tpages></addata></record> |
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source | Web of Science - Science Citation Index Expanded - 1992<img src="https://exlibris-pub.s3.amazonaws.com/fromwos-v2.jpg" />; Access via ScienceDirect (Elsevier) |
subjects | Applied sciences Condensed matter: structure, mechanical and thermal properties Equations of state, phase equilibria, and phase transitions Exact sciences and technology Materials Science Materials Science, Multidisciplinary Metals. Metallurgy Physics Science & Technology Specific phase transitions Technology |
title | Correlation between thermal, kinetic, magnetic and electric effects in the crystallization process of amorphous magnetic alloys |
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