Effects of molybdenum concentration and valence state on the structural and magnetic properties of BaFe11.6MoxZn0.4−xO19 hexaferrites
Barium hexaferrites BaFe 11.6 Mo x Zn 0.4− x O 19 ( x = 0.1, 0.2, 0.4) were prepared by precipitation of the precursors using wet chemical mixture method and then sintering the dried powders at 1100 °C. The properties of the prepared samples were investigated using X-ray diffraction (XRD), scanning...
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creator | Dushaq, G. H. Mahmood, S. H. Bsoul, I. Juwhari, H. K. Lahlouh, B. AlDamen, M. A. |
description | Barium hexaferrites BaFe
11.6
Mo
x
Zn
0.4−
x
O
19
(
x
= 0.1, 0.2, 0.4) were prepared by precipitation of the precursors using wet chemical mixture method and then sintering the dried powders at 1100 °C. The properties of the prepared samples were investigated using X-ray diffraction (XRD), scanning electron microscopy (SEM), vibrating sample magnetometer, and Mössbauer spectroscopy. XRD patterns revealed that all prepared samples had BaFe
12
O
19
hexaferrite structure as a majority phase. SEM images demonstated that the samples consisted mainly of hexagonal platelet-like grains with diameters ranging from 100 to 500 nm. Mössbauer spectra revealed that Zn
2+
ions occupy 4
f
1
sites leading to the splitting of the 12
k
component. However Mo
6+
ions occupy 2
b
sites while Mo
4+
prefer 4
f
1
and 12
k
sites. For the sample with
x
= 0.4,Mo
6+
and Mo
4+
ions were found to have preference for 2
b
and 12
k
sites, respectively, and to induce the development of Fe
2+
ions in the hexaferrite, leading to noticeable changes in the magnetic properties of the system. The observed magnetic properties were found to be consistent with the preferential site occupation of metal ions, and the hyperfine fields derived from Mössbauer spectra of these samples. |
doi_str_mv | 10.1007/s40195-013-0075-2 |
format | Article |
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11.6
Mo
x
Zn
0.4−
x
O
19
(
x
= 0.1, 0.2, 0.4) were prepared by precipitation of the precursors using wet chemical mixture method and then sintering the dried powders at 1100 °C. The properties of the prepared samples were investigated using X-ray diffraction (XRD), scanning electron microscopy (SEM), vibrating sample magnetometer, and Mössbauer spectroscopy. XRD patterns revealed that all prepared samples had BaFe
12
O
19
hexaferrite structure as a majority phase. SEM images demonstated that the samples consisted mainly of hexagonal platelet-like grains with diameters ranging from 100 to 500 nm. Mössbauer spectra revealed that Zn
2+
ions occupy 4
f
1
sites leading to the splitting of the 12
k
component. However Mo
6+
ions occupy 2
b
sites while Mo
4+
prefer 4
f
1
and 12
k
sites. For the sample with
x
= 0.4,Mo
6+
and Mo
4+
ions were found to have preference for 2
b
and 12
k
sites, respectively, and to induce the development of Fe
2+
ions in the hexaferrite, leading to noticeable changes in the magnetic properties of the system. The observed magnetic properties were found to be consistent with the preferential site occupation of metal ions, and the hyperfine fields derived from Mössbauer spectra of these samples.</description><identifier>ISSN: 1006-7191</identifier><identifier>EISSN: 2194-1289</identifier><identifier>DOI: 10.1007/s40195-013-0075-2</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Barium hexaferrite ; Characterization and Evaluation of Materials ; Chemistry and Materials Science ; Corrosion and Coatings ; Hyperfine structure ; Magnetic properties ; Materials Science ; Metallic Materials ; Mossbauer spectroscopy ; Nanotechnology ; Organometallic Chemistry ; Scanning electron microscopy ; Sintering (powder metallurgy) ; Spectra ; Spectroscopy/Spectrometry ; Spectrum analysis ; Tribology ; Valence ; X-ray diffraction</subject><ispartof>Acta metallurgica sinica : English letters, 2013-10, Vol.26 (5), p.509-516</ispartof><rights>The Chinese Society for Metals and Springer-Verlag Berlin Heidelberg 2013</rights><rights>The Chinese Society for Metals and Springer-Verlag Berlin Heidelberg 2013.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s40195-013-0075-2$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2932502762?pq-origsite=primo$$EHTML$$P50$$Gproquest$$H</linktohtml><link.rule.ids>315,781,785,21392,27928,27929,33748,41492,42561,43809,51323,64389,64393,72473</link.rule.ids></links><search><creatorcontrib>Dushaq, G. H.</creatorcontrib><creatorcontrib>Mahmood, S. H.</creatorcontrib><creatorcontrib>Bsoul, I.</creatorcontrib><creatorcontrib>Juwhari, H. K.</creatorcontrib><creatorcontrib>Lahlouh, B.</creatorcontrib><creatorcontrib>AlDamen, M. A.</creatorcontrib><title>Effects of molybdenum concentration and valence state on the structural and magnetic properties of BaFe11.6MoxZn0.4−xO19 hexaferrites</title><title>Acta metallurgica sinica : English letters</title><addtitle>ACTA METALL SIN</addtitle><description>Barium hexaferrites BaFe
11.6
Mo
x
Zn
0.4−
x
O
19
(
x
= 0.1, 0.2, 0.4) were prepared by precipitation of the precursors using wet chemical mixture method and then sintering the dried powders at 1100 °C. The properties of the prepared samples were investigated using X-ray diffraction (XRD), scanning electron microscopy (SEM), vibrating sample magnetometer, and Mössbauer spectroscopy. XRD patterns revealed that all prepared samples had BaFe
12
O
19
hexaferrite structure as a majority phase. SEM images demonstated that the samples consisted mainly of hexagonal platelet-like grains with diameters ranging from 100 to 500 nm. Mössbauer spectra revealed that Zn
2+
ions occupy 4
f
1
sites leading to the splitting of the 12
k
component. However Mo
6+
ions occupy 2
b
sites while Mo
4+
prefer 4
f
1
and 12
k
sites. For the sample with
x
= 0.4,Mo
6+
and Mo
4+
ions were found to have preference for 2
b
and 12
k
sites, respectively, and to induce the development of Fe
2+
ions in the hexaferrite, leading to noticeable changes in the magnetic properties of the system. The observed magnetic properties were found to be consistent with the preferential site occupation of metal ions, and the hyperfine fields derived from Mössbauer spectra of these samples.</description><subject>Barium hexaferrite</subject><subject>Characterization and Evaluation of Materials</subject><subject>Chemistry and Materials Science</subject><subject>Corrosion and Coatings</subject><subject>Hyperfine structure</subject><subject>Magnetic properties</subject><subject>Materials Science</subject><subject>Metallic Materials</subject><subject>Mossbauer spectroscopy</subject><subject>Nanotechnology</subject><subject>Organometallic Chemistry</subject><subject>Scanning electron microscopy</subject><subject>Sintering (powder metallurgy)</subject><subject>Spectra</subject><subject>Spectroscopy/Spectrometry</subject><subject>Spectrum analysis</subject><subject>Tribology</subject><subject>Valence</subject><subject>X-ray diffraction</subject><issn>1006-7191</issn><issn>2194-1289</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNpFkE1OwzAQhS0EEqVwAHaWWKd47MTBS6jKj1TEBjZsIscZl6DUKbaDyglgzRE5CW6LxGrmPX16M3qEnAKbAGPlecgZqCJjILIki4zvkREHlWfAL9Q-GSVIZiUoOCRHIbwmxfOiHJHPmbVoYqC9pcu--6gbdMOSmt4ZdNHr2PaOatfQd91h8miIOiJNZnzZCD-YOHjdbZmlXjiMraEr36_Qxxa3uVf6GgEm8r5fPzs2yX--vtcPoOgLrrVF79uI4ZgcWN0FPPmbY_J0PXuc3mbzh5u76eU8W0EhY1Yrbmpdai4liEYqbgveSAMoWY2agdWlwaYGDVZcCCnSoqwwtcE8t1IZMSZnu9z04tuAIVav_eBdOllxJXjBeCl5oviOCivfugX6fwpYtSm82hVepcKrTeEVF7_4JnZs</recordid><startdate>20131001</startdate><enddate>20131001</enddate><creator>Dushaq, G. H.</creator><creator>Mahmood, S. H.</creator><creator>Bsoul, I.</creator><creator>Juwhari, H. K.</creator><creator>Lahlouh, B.</creator><creator>AlDamen, M. A.</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><scope>8FE</scope><scope>8FG</scope><scope>ABJCF</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>HCIFZ</scope><scope>KB.</scope><scope>PDBOC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope></search><sort><creationdate>20131001</creationdate><title>Effects of molybdenum concentration and valence state on the structural and magnetic properties of BaFe11.6MoxZn0.4−xO19 hexaferrites</title><author>Dushaq, G. H. ; Mahmood, S. H. ; Bsoul, I. ; Juwhari, H. K. ; Lahlouh, B. ; AlDamen, M. A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p156t-b92cba7a26613d692f52d6c1e60bea01fa7cedb1a1f383631a19f3cbce44f69c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Barium hexaferrite</topic><topic>Characterization and Evaluation of Materials</topic><topic>Chemistry and Materials Science</topic><topic>Corrosion and Coatings</topic><topic>Hyperfine structure</topic><topic>Magnetic properties</topic><topic>Materials Science</topic><topic>Metallic Materials</topic><topic>Mossbauer spectroscopy</topic><topic>Nanotechnology</topic><topic>Organometallic Chemistry</topic><topic>Scanning electron microscopy</topic><topic>Sintering (powder metallurgy)</topic><topic>Spectra</topic><topic>Spectroscopy/Spectrometry</topic><topic>Spectrum analysis</topic><topic>Tribology</topic><topic>Valence</topic><topic>X-ray diffraction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dushaq, G. H.</creatorcontrib><creatorcontrib>Mahmood, S. H.</creatorcontrib><creatorcontrib>Bsoul, I.</creatorcontrib><creatorcontrib>Juwhari, H. K.</creatorcontrib><creatorcontrib>Lahlouh, B.</creatorcontrib><creatorcontrib>AlDamen, M. A.</creatorcontrib><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>SciTech Premium Collection</collection><collection>Materials Science Database</collection><collection>Materials Science Collection</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><jtitle>Acta metallurgica sinica : English letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dushaq, G. H.</au><au>Mahmood, S. H.</au><au>Bsoul, I.</au><au>Juwhari, H. K.</au><au>Lahlouh, B.</au><au>AlDamen, M. A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of molybdenum concentration and valence state on the structural and magnetic properties of BaFe11.6MoxZn0.4−xO19 hexaferrites</atitle><jtitle>Acta metallurgica sinica : English letters</jtitle><stitle>ACTA METALL SIN</stitle><date>2013-10-01</date><risdate>2013</risdate><volume>26</volume><issue>5</issue><spage>509</spage><epage>516</epage><pages>509-516</pages><issn>1006-7191</issn><eissn>2194-1289</eissn><abstract>Barium hexaferrites BaFe
11.6
Mo
x
Zn
0.4−
x
O
19
(
x
= 0.1, 0.2, 0.4) were prepared by precipitation of the precursors using wet chemical mixture method and then sintering the dried powders at 1100 °C. The properties of the prepared samples were investigated using X-ray diffraction (XRD), scanning electron microscopy (SEM), vibrating sample magnetometer, and Mössbauer spectroscopy. XRD patterns revealed that all prepared samples had BaFe
12
O
19
hexaferrite structure as a majority phase. SEM images demonstated that the samples consisted mainly of hexagonal platelet-like grains with diameters ranging from 100 to 500 nm. Mössbauer spectra revealed that Zn
2+
ions occupy 4
f
1
sites leading to the splitting of the 12
k
component. However Mo
6+
ions occupy 2
b
sites while Mo
4+
prefer 4
f
1
and 12
k
sites. For the sample with
x
= 0.4,Mo
6+
and Mo
4+
ions were found to have preference for 2
b
and 12
k
sites, respectively, and to induce the development of Fe
2+
ions in the hexaferrite, leading to noticeable changes in the magnetic properties of the system. The observed magnetic properties were found to be consistent with the preferential site occupation of metal ions, and the hyperfine fields derived from Mössbauer spectra of these samples.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><doi>10.1007/s40195-013-0075-2</doi><tpages>8</tpages></addata></record> |
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source | SpringerNature Journals; ProQuest Central UK/Ireland; Alma/SFX Local Collection; ProQuest Central |
subjects | Barium hexaferrite Characterization and Evaluation of Materials Chemistry and Materials Science Corrosion and Coatings Hyperfine structure Magnetic properties Materials Science Metallic Materials Mossbauer spectroscopy Nanotechnology Organometallic Chemistry Scanning electron microscopy Sintering (powder metallurgy) Spectra Spectroscopy/Spectrometry Spectrum analysis Tribology Valence X-ray diffraction |
title | Effects of molybdenum concentration and valence state on the structural and magnetic properties of BaFe11.6MoxZn0.4−xO19 hexaferrites |
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