Influence of competing reactions on the extent of the β-to-α massive transformation in Ag-Cd, Ag-Zn, and Cu-Zn alloys

J. D. Ayers; T. B. Massalski

doi:10.1007/bf02680605

Influence of competing reactions on the extent of the β-to-α massive transformation in Ag-Cd, Ag-Zn, and Cu-Zn alloys

Metallurgical and Materials Transactions B ◽

10.1007/bf02680605 ◽

1972 ◽

Vol 3 (1) ◽

pp. 261-271 ◽

Cited By ~ 31

Author(s):

J. D. Ayers ◽

T. B. Massalski

Keyword(s):

Massive Transformation ◽

Zn Alloys ◽

Competing Reactions

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Observations concerning the β→αm massive transformation in Cu-Zn alloys

Metallurgical Transactions A ◽

10.1007/bf02643450 ◽

1970 ◽

Vol 1 (8) ◽

pp. 2315-2322 ◽

Cited By ~ 56

Author(s):

E. B. Hawbolt ◽

T. B. Massalski

Keyword(s):

Massive Transformation ◽

Zn Alloys

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The Massive Transformation in Cu-Zn Alloys

The Selected Works of John W. Cahn ◽

10.1002/9781118788295.ch23 ◽

2013 ◽

pp. 231-235

Author(s):

David A. Karlyn ◽

John W. Cahn ◽

Morris Cohen

Keyword(s):

Massive Transformation ◽

Zn Alloys

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Effects of Cr and Zn on the interfacial microstructures of borides in Fe–Cr–B cast steels during hot-dipping in Al–Zn alloys

International Journal of Materials Research (formerly Zeitschrift fuer Metallkunde) ◽

10.3139/146.111742 ◽

2019 ◽

Author(s):

Xianman Zhang ◽

Weiping Chen ◽

Hongfeng Luo ◽

Shuang Li ◽

Teng Zhou

Keyword(s):

Cast Steels ◽

Zn Alloys

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Ab Initio Molecular Dynamics Simulation of the Amorphous Structure of Ca-Mg-Cu and Ca-Mg-Zn Alloys (Preprint)

10.21236/ada566094 ◽

2012 ◽

Author(s):

O. N. Senkov ◽

Y. Q. Cheng

Keyword(s):

Molecular Dynamics ◽

Molecular Dynamics Simulation ◽

Ab Initio ◽

Amorphous Structure ◽

Dynamics Simulation ◽

Ab Initio Molecular Dynamics ◽

Zn Alloys

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Thermodynamic, Kinetic, and Physical Properties of Ag-Al-Cu-Ni-Si-Zn Alloys

10.2172/1440721 ◽

2018 ◽

Author(s):

Patrice E. A. Turchi

Keyword(s):

Physical Properties ◽

Zn Alloys

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Participation of 19-substituents in electrophilic additions. influence of 3β-substitution on hypobromous acid addition to 5,6-unsaturated steroids

Collection of Czechoslovak Chemical Communications ◽

10.1135/cccc19803023 ◽

1980 ◽

Vol 45 (11) ◽

pp. 3023-3029 ◽

Cited By ~ 4

Author(s):

Pavel Kočovský ◽

Václav Černý

Keyword(s):

Acid Addition ◽

Hypobromous Acid ◽

Electrophilic Additions ◽

Competing Reactions

Reactions of 19-hydroxy-, methoxy- and acetoxy-5-cholestenes Ia, IIa, IIIa were studied and compared with those previously obtained with analogous 3β-acetoxy-19-substituted 5-cholestenes Ib, IIb, IIIc. A marked difference was found in 19-acetoxy derivatives where the 3-unsubstituted compound IIIa yields exclusively the bromohydrin XVIa as a product of 6(O)π,n participation while the 3β-acetoxy derivative IIIb gives, apart from the analogous bromohydrin XVIb, also products of competing reactions: The epoxide XIIb and the bromohydrin XIIIb.

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