Synthesis and characterization of new bimetallic transition metal oxynitrides: $ M_{I} $-$ M_{II} $-O-N ($ M_{I} $, $ M_{II} $=V, Mo, W and Nb)
Abstract A new class of materials, $ M_{I} $-$ M_{II} $-O-N (where $ M_{I} $, $ M_{II} $ = V, Mo, W, and Nb), has been synthesized by nitriding bimetallic oxide precursors with ammonia gas via a temperature programmed reaction. The oxide precursors are prepared by conventional solid state reaction b...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Yu, C. C. [verfasserIn] |
|---|
| Format: |
Artikel |
|---|---|
| Sprache: |
Englisch |
| Erschienen: |
1995 |
|---|
| Schlagwörter: |
|---|
| Anmerkung: |
© Chapman & Hall 1995 |
|---|
| Übergeordnetes Werk: |
Enthalten in: Journal of materials science - Kluwer Academic Publishers-Plenum Publishers, 1966, 30(1995), 16 vom: Aug., Seite 4037-4042 |
|---|---|
| Übergeordnetes Werk: |
volume:30 ; year:1995 ; number:16 ; month:08 ; pages:4037-4042 |
| Links: |
|---|
| DOI / URN: |
10.1007/BF00360706 |
|---|
| Katalog-ID: |
OLC2046220358 |
|---|
| LEADER | 01000caa a22002652 4500 | ||
|---|---|---|---|
| 001 | OLC2046220358 | ||
| 003 | DE-627 | ||
| 005 | 20230503122544.0 | ||
| 007 | tu | ||
| 008 | 200820s1995 xx ||||| 00| ||eng c | ||
| 024 | 7 | |a 10.1007/BF00360706 |2 doi | |
| 035 | |a (DE-627)OLC2046220358 | ||
| 035 | |a (DE-He213)BF00360706-p | ||
| 040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
| 041 | |a eng | ||
| 082 | 0 | 4 | |a 670 |q VZ |
| 100 | 1 | |a Yu, C. C. |e verfasserin |4 aut | |
| 245 | 1 | 0 | |a Synthesis and characterization of new bimetallic transition metal oxynitrides: $ M_{I} $-$ M_{II} $-O-N ($ M_{I} $, $ M_{II} $=V, Mo, W and Nb) |
| 264 | 1 | |c 1995 | |
| 336 | |a Text |b txt |2 rdacontent | ||
| 337 | |a ohne Hilfsmittel zu benutzen |b n |2 rdamedia | ||
| 338 | |a Band |b nc |2 rdacarrier | ||
| 500 | |a © Chapman & Hall 1995 | ||
| 520 | |a Abstract A new class of materials, $ M_{I} $-$ M_{II} $-O-N (where $ M_{I} $, $ M_{II} $ = V, Mo, W, and Nb), has been synthesized by nitriding bimetallic oxide precursors with ammonia gas via a temperature programmed reaction. The oxide precursors are prepared by conventional solid state reaction between two appropriate monometallic oxides. The synthesis of the oxynitrides involves passing $ NH_{3} $ gas over the oxide precursors at a flow rate of 6.80×$ 10^{2} $ $ μmols^{−1} $ (1000 $ cm^{3} $ $ min^{−1} $), and raising the temperature at a rate of 8.3×$ 10^{−2} $ $ Ks^{−1} $ (5K $ min^{−1} $) to a final temperature which is held constant for a short period of time. The oxynitrides thus obtained are pyrophoric and need to be passivated before exposing them to air. All these new bimetallic oxynitrides have a face centered cubic (f.c.c.) metal arrangement and high values of surface area. Their surface activity is assessed from their ability to chemisorb CO. | ||
| 650 | 4 | |a Polymer | |
| 650 | 4 | |a Solid State | |
| 650 | 4 | |a Surface Activity | |
| 650 | 4 | |a Material Processing | |
| 650 | 4 | |a Solid State Reaction | |
| 700 | 1 | |a Oyama, S. T. |4 aut | |
| 773 | 0 | 8 | |i Enthalten in |t Journal of materials science |d Kluwer Academic Publishers-Plenum Publishers, 1966 |g 30(1995), 16 vom: Aug., Seite 4037-4042 |w (DE-627)129546372 |w (DE-600)218324-9 |w (DE-576)014996774 |x 0022-2461 |7 nnns |
| 773 | 1 | 8 | |g volume:30 |g year:1995 |g number:16 |g month:08 |g pages:4037-4042 |
| 856 | 4 | 1 | |u https://doi.org/10.1007/BF00360706 |z lizenzpflichtig |3 Volltext |
| 912 | |a GBV_USEFLAG_A | ||
| 912 | |a SYSFLAG_A | ||
| 912 | |a GBV_OLC | ||
| 912 | |a SSG-OLC-TEC | ||
| 912 | |a GBV_ILN_11 | ||
| 912 | |a GBV_ILN_20 | ||
| 912 | |a GBV_ILN_23 | ||
| 912 | |a GBV_ILN_24 | ||
| 912 | |a GBV_ILN_30 | ||
| 912 | |a GBV_ILN_32 | ||
| 912 | |a GBV_ILN_40 | ||
| 912 | |a GBV_ILN_62 | ||
| 912 | |a GBV_ILN_65 | ||
| 912 | |a GBV_ILN_70 | ||
| 912 | |a GBV_ILN_2004 | ||
| 912 | |a GBV_ILN_2006 | ||
| 912 | |a GBV_ILN_2015 | ||
| 912 | |a GBV_ILN_2020 | ||
| 912 | |a GBV_ILN_2021 | ||
| 912 | |a GBV_ILN_4082 | ||
| 912 | |a GBV_ILN_4305 | ||
| 912 | |a GBV_ILN_4306 | ||
| 912 | |a GBV_ILN_4316 | ||
| 912 | |a GBV_ILN_4319 | ||
| 912 | |a GBV_ILN_4323 | ||
| 912 | |a GBV_ILN_4700 | ||
| 951 | |a AR | ||
| 952 | |d 30 |j 1995 |e 16 |c 08 |h 4037-4042 | ||
| author_variant |
c c y cc ccy s t o st sto |
|---|---|
| matchkey_str |
article:00222461:1995----::yteiadhrceiainfebmtlitastomtlxntie |
| hierarchy_sort_str |
1995 |
| publishDate |
1995 |
| allfields |
10.1007/BF00360706 doi (DE-627)OLC2046220358 (DE-He213)BF00360706-p DE-627 ger DE-627 rakwb eng 670 VZ Yu, C. C. verfasserin aut Synthesis and characterization of new bimetallic transition metal oxynitrides: $ M_{I} $-$ M_{II} $-O-N ($ M_{I} $, $ M_{II} $=V, Mo, W and Nb) 1995 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © Chapman & Hall 1995 Abstract A new class of materials, $ M_{I} $-$ M_{II} $-O-N (where $ M_{I} $, $ M_{II} $ = V, Mo, W, and Nb), has been synthesized by nitriding bimetallic oxide precursors with ammonia gas via a temperature programmed reaction. The oxide precursors are prepared by conventional solid state reaction between two appropriate monometallic oxides. The synthesis of the oxynitrides involves passing $ NH_{3} $ gas over the oxide precursors at a flow rate of 6.80×$ 10^{2} $ $ μmols^{−1} $ (1000 $ cm^{3} $ $ min^{−1} $), and raising the temperature at a rate of 8.3×$ 10^{−2} $ $ Ks^{−1} $ (5K $ min^{−1} $) to a final temperature which is held constant for a short period of time. The oxynitrides thus obtained are pyrophoric and need to be passivated before exposing them to air. All these new bimetallic oxynitrides have a face centered cubic (f.c.c.) metal arrangement and high values of surface area. Their surface activity is assessed from their ability to chemisorb CO. Polymer Solid State Surface Activity Material Processing Solid State Reaction Oyama, S. T. aut Enthalten in Journal of materials science Kluwer Academic Publishers-Plenum Publishers, 1966 30(1995), 16 vom: Aug., Seite 4037-4042 (DE-627)129546372 (DE-600)218324-9 (DE-576)014996774 0022-2461 nnns volume:30 year:1995 number:16 month:08 pages:4037-4042 https://doi.org/10.1007/BF00360706 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC GBV_ILN_11 GBV_ILN_20 GBV_ILN_23 GBV_ILN_24 GBV_ILN_30 GBV_ILN_32 GBV_ILN_40 GBV_ILN_62 GBV_ILN_65 GBV_ILN_70 GBV_ILN_2004 GBV_ILN_2006 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_4082 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4316 GBV_ILN_4319 GBV_ILN_4323 GBV_ILN_4700 AR 30 1995 16 08 4037-4042 |
| spelling |
10.1007/BF00360706 doi (DE-627)OLC2046220358 (DE-He213)BF00360706-p DE-627 ger DE-627 rakwb eng 670 VZ Yu, C. C. verfasserin aut Synthesis and characterization of new bimetallic transition metal oxynitrides: $ M_{I} $-$ M_{II} $-O-N ($ M_{I} $, $ M_{II} $=V, Mo, W and Nb) 1995 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © Chapman & Hall 1995 Abstract A new class of materials, $ M_{I} $-$ M_{II} $-O-N (where $ M_{I} $, $ M_{II} $ = V, Mo, W, and Nb), has been synthesized by nitriding bimetallic oxide precursors with ammonia gas via a temperature programmed reaction. The oxide precursors are prepared by conventional solid state reaction between two appropriate monometallic oxides. The synthesis of the oxynitrides involves passing $ NH_{3} $ gas over the oxide precursors at a flow rate of 6.80×$ 10^{2} $ $ μmols^{−1} $ (1000 $ cm^{3} $ $ min^{−1} $), and raising the temperature at a rate of 8.3×$ 10^{−2} $ $ Ks^{−1} $ (5K $ min^{−1} $) to a final temperature which is held constant for a short period of time. The oxynitrides thus obtained are pyrophoric and need to be passivated before exposing them to air. All these new bimetallic oxynitrides have a face centered cubic (f.c.c.) metal arrangement and high values of surface area. Their surface activity is assessed from their ability to chemisorb CO. Polymer Solid State Surface Activity Material Processing Solid State Reaction Oyama, S. T. aut Enthalten in Journal of materials science Kluwer Academic Publishers-Plenum Publishers, 1966 30(1995), 16 vom: Aug., Seite 4037-4042 (DE-627)129546372 (DE-600)218324-9 (DE-576)014996774 0022-2461 nnns volume:30 year:1995 number:16 month:08 pages:4037-4042 https://doi.org/10.1007/BF00360706 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC GBV_ILN_11 GBV_ILN_20 GBV_ILN_23 GBV_ILN_24 GBV_ILN_30 GBV_ILN_32 GBV_ILN_40 GBV_ILN_62 GBV_ILN_65 GBV_ILN_70 GBV_ILN_2004 GBV_ILN_2006 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_4082 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4316 GBV_ILN_4319 GBV_ILN_4323 GBV_ILN_4700 AR 30 1995 16 08 4037-4042 |
| allfields_unstemmed |
10.1007/BF00360706 doi (DE-627)OLC2046220358 (DE-He213)BF00360706-p DE-627 ger DE-627 rakwb eng 670 VZ Yu, C. C. verfasserin aut Synthesis and characterization of new bimetallic transition metal oxynitrides: $ M_{I} $-$ M_{II} $-O-N ($ M_{I} $, $ M_{II} $=V, Mo, W and Nb) 1995 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © Chapman & Hall 1995 Abstract A new class of materials, $ M_{I} $-$ M_{II} $-O-N (where $ M_{I} $, $ M_{II} $ = V, Mo, W, and Nb), has been synthesized by nitriding bimetallic oxide precursors with ammonia gas via a temperature programmed reaction. The oxide precursors are prepared by conventional solid state reaction between two appropriate monometallic oxides. The synthesis of the oxynitrides involves passing $ NH_{3} $ gas over the oxide precursors at a flow rate of 6.80×$ 10^{2} $ $ μmols^{−1} $ (1000 $ cm^{3} $ $ min^{−1} $), and raising the temperature at a rate of 8.3×$ 10^{−2} $ $ Ks^{−1} $ (5K $ min^{−1} $) to a final temperature which is held constant for a short period of time. The oxynitrides thus obtained are pyrophoric and need to be passivated before exposing them to air. All these new bimetallic oxynitrides have a face centered cubic (f.c.c.) metal arrangement and high values of surface area. Their surface activity is assessed from their ability to chemisorb CO. Polymer Solid State Surface Activity Material Processing Solid State Reaction Oyama, S. T. aut Enthalten in Journal of materials science Kluwer Academic Publishers-Plenum Publishers, 1966 30(1995), 16 vom: Aug., Seite 4037-4042 (DE-627)129546372 (DE-600)218324-9 (DE-576)014996774 0022-2461 nnns volume:30 year:1995 number:16 month:08 pages:4037-4042 https://doi.org/10.1007/BF00360706 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC GBV_ILN_11 GBV_ILN_20 GBV_ILN_23 GBV_ILN_24 GBV_ILN_30 GBV_ILN_32 GBV_ILN_40 GBV_ILN_62 GBV_ILN_65 GBV_ILN_70 GBV_ILN_2004 GBV_ILN_2006 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_4082 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4316 GBV_ILN_4319 GBV_ILN_4323 GBV_ILN_4700 AR 30 1995 16 08 4037-4042 |
| allfieldsGer |
10.1007/BF00360706 doi (DE-627)OLC2046220358 (DE-He213)BF00360706-p DE-627 ger DE-627 rakwb eng 670 VZ Yu, C. C. verfasserin aut Synthesis and characterization of new bimetallic transition metal oxynitrides: $ M_{I} $-$ M_{II} $-O-N ($ M_{I} $, $ M_{II} $=V, Mo, W and Nb) 1995 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © Chapman & Hall 1995 Abstract A new class of materials, $ M_{I} $-$ M_{II} $-O-N (where $ M_{I} $, $ M_{II} $ = V, Mo, W, and Nb), has been synthesized by nitriding bimetallic oxide precursors with ammonia gas via a temperature programmed reaction. The oxide precursors are prepared by conventional solid state reaction between two appropriate monometallic oxides. The synthesis of the oxynitrides involves passing $ NH_{3} $ gas over the oxide precursors at a flow rate of 6.80×$ 10^{2} $ $ μmols^{−1} $ (1000 $ cm^{3} $ $ min^{−1} $), and raising the temperature at a rate of 8.3×$ 10^{−2} $ $ Ks^{−1} $ (5K $ min^{−1} $) to a final temperature which is held constant for a short period of time. The oxynitrides thus obtained are pyrophoric and need to be passivated before exposing them to air. All these new bimetallic oxynitrides have a face centered cubic (f.c.c.) metal arrangement and high values of surface area. Their surface activity is assessed from their ability to chemisorb CO. Polymer Solid State Surface Activity Material Processing Solid State Reaction Oyama, S. T. aut Enthalten in Journal of materials science Kluwer Academic Publishers-Plenum Publishers, 1966 30(1995), 16 vom: Aug., Seite 4037-4042 (DE-627)129546372 (DE-600)218324-9 (DE-576)014996774 0022-2461 nnns volume:30 year:1995 number:16 month:08 pages:4037-4042 https://doi.org/10.1007/BF00360706 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC GBV_ILN_11 GBV_ILN_20 GBV_ILN_23 GBV_ILN_24 GBV_ILN_30 GBV_ILN_32 GBV_ILN_40 GBV_ILN_62 GBV_ILN_65 GBV_ILN_70 GBV_ILN_2004 GBV_ILN_2006 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_4082 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4316 GBV_ILN_4319 GBV_ILN_4323 GBV_ILN_4700 AR 30 1995 16 08 4037-4042 |
| allfieldsSound |
10.1007/BF00360706 doi (DE-627)OLC2046220358 (DE-He213)BF00360706-p DE-627 ger DE-627 rakwb eng 670 VZ Yu, C. C. verfasserin aut Synthesis and characterization of new bimetallic transition metal oxynitrides: $ M_{I} $-$ M_{II} $-O-N ($ M_{I} $, $ M_{II} $=V, Mo, W and Nb) 1995 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © Chapman & Hall 1995 Abstract A new class of materials, $ M_{I} $-$ M_{II} $-O-N (where $ M_{I} $, $ M_{II} $ = V, Mo, W, and Nb), has been synthesized by nitriding bimetallic oxide precursors with ammonia gas via a temperature programmed reaction. The oxide precursors are prepared by conventional solid state reaction between two appropriate monometallic oxides. The synthesis of the oxynitrides involves passing $ NH_{3} $ gas over the oxide precursors at a flow rate of 6.80×$ 10^{2} $ $ μmols^{−1} $ (1000 $ cm^{3} $ $ min^{−1} $), and raising the temperature at a rate of 8.3×$ 10^{−2} $ $ Ks^{−1} $ (5K $ min^{−1} $) to a final temperature which is held constant for a short period of time. The oxynitrides thus obtained are pyrophoric and need to be passivated before exposing them to air. All these new bimetallic oxynitrides have a face centered cubic (f.c.c.) metal arrangement and high values of surface area. Their surface activity is assessed from their ability to chemisorb CO. Polymer Solid State Surface Activity Material Processing Solid State Reaction Oyama, S. T. aut Enthalten in Journal of materials science Kluwer Academic Publishers-Plenum Publishers, 1966 30(1995), 16 vom: Aug., Seite 4037-4042 (DE-627)129546372 (DE-600)218324-9 (DE-576)014996774 0022-2461 nnns volume:30 year:1995 number:16 month:08 pages:4037-4042 https://doi.org/10.1007/BF00360706 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC GBV_ILN_11 GBV_ILN_20 GBV_ILN_23 GBV_ILN_24 GBV_ILN_30 GBV_ILN_32 GBV_ILN_40 GBV_ILN_62 GBV_ILN_65 GBV_ILN_70 GBV_ILN_2004 GBV_ILN_2006 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_4082 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4316 GBV_ILN_4319 GBV_ILN_4323 GBV_ILN_4700 AR 30 1995 16 08 4037-4042 |
| language |
English |
| source |
Enthalten in Journal of materials science 30(1995), 16 vom: Aug., Seite 4037-4042 volume:30 year:1995 number:16 month:08 pages:4037-4042 |
| sourceStr |
Enthalten in Journal of materials science 30(1995), 16 vom: Aug., Seite 4037-4042 volume:30 year:1995 number:16 month:08 pages:4037-4042 |
| format_phy_str_mv |
Article |
| institution |
findex.gbv.de |
| topic_facet |
Polymer Solid State Surface Activity Material Processing Solid State Reaction |
| dewey-raw |
670 |
| isfreeaccess_bool |
false |
| container_title |
Journal of materials science |
| authorswithroles_txt_mv |
Yu, C. C. @@aut@@ Oyama, S. T. @@aut@@ |
| publishDateDaySort_date |
1995-08-01T00:00:00Z |
| hierarchy_top_id |
129546372 |
| dewey-sort |
3670 |
| id |
OLC2046220358 |
| language_de |
englisch |
| fullrecord |
<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">OLC2046220358</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20230503122544.0</controlfield><controlfield tag="007">tu</controlfield><controlfield tag="008">200820s1995 xx ||||| 00| ||eng c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1007/BF00360706</subfield><subfield code="2">doi</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)OLC2046220358</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-He213)BF00360706-p</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rakwb</subfield></datafield><datafield tag="041" ind1=" " ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="082" ind1="0" ind2="4"><subfield code="a">670</subfield><subfield code="q">VZ</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Yu, C. C.</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Synthesis and characterization of new bimetallic transition metal oxynitrides: $ M_{I} $-$ M_{II} $-O-N ($ M_{I} $, $ M_{II} $=V, Mo, W and Nb)</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">1995</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">Text</subfield><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">ohne Hilfsmittel zu benutzen</subfield><subfield code="b">n</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">Band</subfield><subfield code="b">nc</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="500" ind1=" " ind2=" "><subfield code="a">© Chapman & Hall 1995</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Abstract A new class of materials, $ M_{I} $-$ M_{II} $-O-N (where $ M_{I} $, $ M_{II} $ = V, Mo, W, and Nb), has been synthesized by nitriding bimetallic oxide precursors with ammonia gas via a temperature programmed reaction. The oxide precursors are prepared by conventional solid state reaction between two appropriate monometallic oxides. The synthesis of the oxynitrides involves passing $ NH_{3} $ gas over the oxide precursors at a flow rate of 6.80×$ 10^{2} $ $ μmols^{−1} $ (1000 $ cm^{3} $ $ min^{−1} $), and raising the temperature at a rate of 8.3×$ 10^{−2} $ $ Ks^{−1} $ (5K $ min^{−1} $) to a final temperature which is held constant for a short period of time. The oxynitrides thus obtained are pyrophoric and need to be passivated before exposing them to air. All these new bimetallic oxynitrides have a face centered cubic (f.c.c.) metal arrangement and high values of surface area. Their surface activity is assessed from their ability to chemisorb CO.</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Polymer</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Solid State</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Surface Activity</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Material Processing</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Solid State Reaction</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Oyama, S. T.</subfield><subfield code="4">aut</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">Enthalten in</subfield><subfield code="t">Journal of materials science</subfield><subfield code="d">Kluwer Academic Publishers-Plenum Publishers, 1966</subfield><subfield code="g">30(1995), 16 vom: Aug., Seite 4037-4042</subfield><subfield code="w">(DE-627)129546372</subfield><subfield code="w">(DE-600)218324-9</subfield><subfield code="w">(DE-576)014996774</subfield><subfield code="x">0022-2461</subfield><subfield code="7">nnns</subfield></datafield><datafield tag="773" ind1="1" ind2="8"><subfield code="g">volume:30</subfield><subfield code="g">year:1995</subfield><subfield code="g">number:16</subfield><subfield code="g">month:08</subfield><subfield code="g">pages:4037-4042</subfield></datafield><datafield tag="856" ind1="4" ind2="1"><subfield code="u">https://doi.org/10.1007/BF00360706</subfield><subfield code="z">lizenzpflichtig</subfield><subfield code="3">Volltext</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_USEFLAG_A</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SYSFLAG_A</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_OLC</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SSG-OLC-TEC</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_11</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_20</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_23</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_24</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_30</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_32</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_40</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_62</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_65</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_70</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2004</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2006</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2015</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2020</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2021</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4082</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4305</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4306</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4316</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4319</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4323</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4700</subfield></datafield><datafield tag="951" ind1=" " ind2=" "><subfield code="a">AR</subfield></datafield><datafield tag="952" ind1=" " ind2=" "><subfield code="d">30</subfield><subfield code="j">1995</subfield><subfield code="e">16</subfield><subfield code="c">08</subfield><subfield code="h">4037-4042</subfield></datafield></record></collection>
|
| author |
Yu, C. C. |
| spellingShingle |
Yu, C. C. ddc 670 misc Polymer misc Solid State misc Surface Activity misc Material Processing misc Solid State Reaction Synthesis and characterization of new bimetallic transition metal oxynitrides: $ M_{I} $-$ M_{II} $-O-N ($ M_{I} $, $ M_{II} $=V, Mo, W and Nb) |
| authorStr |
Yu, C. C. |
| ppnlink_with_tag_str_mv |
@@773@@(DE-627)129546372 |
| format |
Article |
| dewey-ones |
670 - Manufacturing |
| delete_txt_mv |
keep |
| author_role |
aut aut |
| collection |
OLC |
| remote_str |
false |
| illustrated |
Not Illustrated |
| issn |
0022-2461 |
| topic_title |
670 VZ Synthesis and characterization of new bimetallic transition metal oxynitrides: $ M_{I} $-$ M_{II} $-O-N ($ M_{I} $, $ M_{II} $=V, Mo, W and Nb) Polymer Solid State Surface Activity Material Processing Solid State Reaction |
| topic |
ddc 670 misc Polymer misc Solid State misc Surface Activity misc Material Processing misc Solid State Reaction |
| topic_unstemmed |
ddc 670 misc Polymer misc Solid State misc Surface Activity misc Material Processing misc Solid State Reaction |
| topic_browse |
ddc 670 misc Polymer misc Solid State misc Surface Activity misc Material Processing misc Solid State Reaction |
| format_facet |
Aufsätze Gedruckte Aufsätze |
| format_main_str_mv |
Text Zeitschrift/Artikel |
| carriertype_str_mv |
nc |
| hierarchy_parent_title |
Journal of materials science |
| hierarchy_parent_id |
129546372 |
| dewey-tens |
670 - Manufacturing |
| hierarchy_top_title |
Journal of materials science |
| isfreeaccess_txt |
false |
| familylinks_str_mv |
(DE-627)129546372 (DE-600)218324-9 (DE-576)014996774 |
| title |
Synthesis and characterization of new bimetallic transition metal oxynitrides: $ M_{I} $-$ M_{II} $-O-N ($ M_{I} $, $ M_{II} $=V, Mo, W and Nb) |
| ctrlnum |
(DE-627)OLC2046220358 (DE-He213)BF00360706-p |
| title_full |
Synthesis and characterization of new bimetallic transition metal oxynitrides: $ M_{I} $-$ M_{II} $-O-N ($ M_{I} $, $ M_{II} $=V, Mo, W and Nb) |
| author_sort |
Yu, C. C. |
| journal |
Journal of materials science |
| journalStr |
Journal of materials science |
| lang_code |
eng |
| isOA_bool |
false |
| dewey-hundreds |
600 - Technology |
| recordtype |
marc |
| publishDateSort |
1995 |
| contenttype_str_mv |
txt |
| container_start_page |
4037 |
| author_browse |
Yu, C. C. Oyama, S. T. |
| container_volume |
30 |
| class |
670 VZ |
| format_se |
Aufsätze |
| author-letter |
Yu, C. C. |
| doi_str_mv |
10.1007/BF00360706 |
| dewey-full |
670 |
| title_sort |
synthesis and characterization of new bimetallic transition metal oxynitrides: $ m_{i} $-$ m_{ii} $-o-n ($ m_{i} $, $ m_{ii} $=v, mo, w and nb) |
| title_auth |
Synthesis and characterization of new bimetallic transition metal oxynitrides: $ M_{I} $-$ M_{II} $-O-N ($ M_{I} $, $ M_{II} $=V, Mo, W and Nb) |
| abstract |
Abstract A new class of materials, $ M_{I} $-$ M_{II} $-O-N (where $ M_{I} $, $ M_{II} $ = V, Mo, W, and Nb), has been synthesized by nitriding bimetallic oxide precursors with ammonia gas via a temperature programmed reaction. The oxide precursors are prepared by conventional solid state reaction between two appropriate monometallic oxides. The synthesis of the oxynitrides involves passing $ NH_{3} $ gas over the oxide precursors at a flow rate of 6.80×$ 10^{2} $ $ μmols^{−1} $ (1000 $ cm^{3} $ $ min^{−1} $), and raising the temperature at a rate of 8.3×$ 10^{−2} $ $ Ks^{−1} $ (5K $ min^{−1} $) to a final temperature which is held constant for a short period of time. The oxynitrides thus obtained are pyrophoric and need to be passivated before exposing them to air. All these new bimetallic oxynitrides have a face centered cubic (f.c.c.) metal arrangement and high values of surface area. Their surface activity is assessed from their ability to chemisorb CO. © Chapman & Hall 1995 |
| abstractGer |
Abstract A new class of materials, $ M_{I} $-$ M_{II} $-O-N (where $ M_{I} $, $ M_{II} $ = V, Mo, W, and Nb), has been synthesized by nitriding bimetallic oxide precursors with ammonia gas via a temperature programmed reaction. The oxide precursors are prepared by conventional solid state reaction between two appropriate monometallic oxides. The synthesis of the oxynitrides involves passing $ NH_{3} $ gas over the oxide precursors at a flow rate of 6.80×$ 10^{2} $ $ μmols^{−1} $ (1000 $ cm^{3} $ $ min^{−1} $), and raising the temperature at a rate of 8.3×$ 10^{−2} $ $ Ks^{−1} $ (5K $ min^{−1} $) to a final temperature which is held constant for a short period of time. The oxynitrides thus obtained are pyrophoric and need to be passivated before exposing them to air. All these new bimetallic oxynitrides have a face centered cubic (f.c.c.) metal arrangement and high values of surface area. Their surface activity is assessed from their ability to chemisorb CO. © Chapman & Hall 1995 |
| abstract_unstemmed |
Abstract A new class of materials, $ M_{I} $-$ M_{II} $-O-N (where $ M_{I} $, $ M_{II} $ = V, Mo, W, and Nb), has been synthesized by nitriding bimetallic oxide precursors with ammonia gas via a temperature programmed reaction. The oxide precursors are prepared by conventional solid state reaction between two appropriate monometallic oxides. The synthesis of the oxynitrides involves passing $ NH_{3} $ gas over the oxide precursors at a flow rate of 6.80×$ 10^{2} $ $ μmols^{−1} $ (1000 $ cm^{3} $ $ min^{−1} $), and raising the temperature at a rate of 8.3×$ 10^{−2} $ $ Ks^{−1} $ (5K $ min^{−1} $) to a final temperature which is held constant for a short period of time. The oxynitrides thus obtained are pyrophoric and need to be passivated before exposing them to air. All these new bimetallic oxynitrides have a face centered cubic (f.c.c.) metal arrangement and high values of surface area. Their surface activity is assessed from their ability to chemisorb CO. © Chapman & Hall 1995 |
| collection_details |
GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC GBV_ILN_11 GBV_ILN_20 GBV_ILN_23 GBV_ILN_24 GBV_ILN_30 GBV_ILN_32 GBV_ILN_40 GBV_ILN_62 GBV_ILN_65 GBV_ILN_70 GBV_ILN_2004 GBV_ILN_2006 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_4082 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4316 GBV_ILN_4319 GBV_ILN_4323 GBV_ILN_4700 |
| container_issue |
16 |
| title_short |
Synthesis and characterization of new bimetallic transition metal oxynitrides: $ M_{I} $-$ M_{II} $-O-N ($ M_{I} $, $ M_{II} $=V, Mo, W and Nb) |
| url |
https://doi.org/10.1007/BF00360706 |
| remote_bool |
false |
| author2 |
Oyama, S. T. |
| author2Str |
Oyama, S. T. |
| ppnlink |
129546372 |
| mediatype_str_mv |
n |
| isOA_txt |
false |
| hochschulschrift_bool |
false |
| doi_str |
10.1007/BF00360706 |
| up_date |
2024-07-04T04:32:24.125Z |
| _version_ |
1803621545144221696 |
| fullrecord_marcxml |
<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">OLC2046220358</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20230503122544.0</controlfield><controlfield tag="007">tu</controlfield><controlfield tag="008">200820s1995 xx ||||| 00| ||eng c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1007/BF00360706</subfield><subfield code="2">doi</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)OLC2046220358</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-He213)BF00360706-p</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rakwb</subfield></datafield><datafield tag="041" ind1=" " ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="082" ind1="0" ind2="4"><subfield code="a">670</subfield><subfield code="q">VZ</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Yu, C. C.</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Synthesis and characterization of new bimetallic transition metal oxynitrides: $ M_{I} $-$ M_{II} $-O-N ($ M_{I} $, $ M_{II} $=V, Mo, W and Nb)</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">1995</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">Text</subfield><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">ohne Hilfsmittel zu benutzen</subfield><subfield code="b">n</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">Band</subfield><subfield code="b">nc</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="500" ind1=" " ind2=" "><subfield code="a">© Chapman & Hall 1995</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Abstract A new class of materials, $ M_{I} $-$ M_{II} $-O-N (where $ M_{I} $, $ M_{II} $ = V, Mo, W, and Nb), has been synthesized by nitriding bimetallic oxide precursors with ammonia gas via a temperature programmed reaction. The oxide precursors are prepared by conventional solid state reaction between two appropriate monometallic oxides. The synthesis of the oxynitrides involves passing $ NH_{3} $ gas over the oxide precursors at a flow rate of 6.80×$ 10^{2} $ $ μmols^{−1} $ (1000 $ cm^{3} $ $ min^{−1} $), and raising the temperature at a rate of 8.3×$ 10^{−2} $ $ Ks^{−1} $ (5K $ min^{−1} $) to a final temperature which is held constant for a short period of time. The oxynitrides thus obtained are pyrophoric and need to be passivated before exposing them to air. All these new bimetallic oxynitrides have a face centered cubic (f.c.c.) metal arrangement and high values of surface area. Their surface activity is assessed from their ability to chemisorb CO.</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Polymer</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Solid State</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Surface Activity</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Material Processing</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Solid State Reaction</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Oyama, S. T.</subfield><subfield code="4">aut</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">Enthalten in</subfield><subfield code="t">Journal of materials science</subfield><subfield code="d">Kluwer Academic Publishers-Plenum Publishers, 1966</subfield><subfield code="g">30(1995), 16 vom: Aug., Seite 4037-4042</subfield><subfield code="w">(DE-627)129546372</subfield><subfield code="w">(DE-600)218324-9</subfield><subfield code="w">(DE-576)014996774</subfield><subfield code="x">0022-2461</subfield><subfield code="7">nnns</subfield></datafield><datafield tag="773" ind1="1" ind2="8"><subfield code="g">volume:30</subfield><subfield code="g">year:1995</subfield><subfield code="g">number:16</subfield><subfield code="g">month:08</subfield><subfield code="g">pages:4037-4042</subfield></datafield><datafield tag="856" ind1="4" ind2="1"><subfield code="u">https://doi.org/10.1007/BF00360706</subfield><subfield code="z">lizenzpflichtig</subfield><subfield code="3">Volltext</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_USEFLAG_A</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SYSFLAG_A</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_OLC</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SSG-OLC-TEC</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_11</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_20</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_23</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_24</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_30</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_32</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_40</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_62</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_65</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_70</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2004</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2006</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2015</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2020</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2021</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4082</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4305</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4306</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4316</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4319</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4323</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4700</subfield></datafield><datafield tag="951" ind1=" " ind2=" "><subfield code="a">AR</subfield></datafield><datafield tag="952" ind1=" " ind2=" "><subfield code="d">30</subfield><subfield code="j">1995</subfield><subfield code="e">16</subfield><subfield code="c">08</subfield><subfield code="h">4037-4042</subfield></datafield></record></collection>
|
| score |
7.399081 |