In situ neutron diffraction study of the reduction of New Zealand ironsands in dilute hydrogen mixtures

被引:10
作者
Longbottom, Raymond James [1 ]
Ingham, Bridget [2 ]
Reid, Mark Henry [3 ]
Studer, Andrew J. [3 ]
Bumby, Christopher W. [4 ]
Monaghan, Brian Joseph [1 ]
机构
[1] Univ Wollongong, Fac Engn & Informat Sci, Pyromet Res Grp, Wollongong, NSW 2522, Australia
[2] Callaghan Innovat, Lower Hutt, New Zealand
[3] Australian Nucl Sci & Technol Org, Australian Ctr Neutron Scattering, Sydney, NSW, Australia
[4] Victoria Univ Wellington, Robinson Res Inst, Lower Hutt, New Zealand
来源
MINERAL PROCESSING AND EXTRACTIVE METALLURGY-TRANSACTIONS OF THE INSTITUTIONS OF MINING AND METALLURGY | 2019年 / 128卷 / 03期
关键词
New Zealand ironsand; titanomagnetite; reduction; hydrogen; direct reduced iron; iron ore; neutron diffraction; in situ measurement; TITANIA-FERROUS ORE; EQUATION-OF-STATE; CURIE-TEMPERATURE; X-RAY; IRON; MAGNETITE; SYSTEM; FE3O4;
D O I
10.1080/03719553.2017.1412877
中图分类号
TD [矿业工程];
学科分类号
0819 ;
摘要
The reduction of New Zealand titanomagnetite ironsand in a dilute hydrogen-nitrogen gas mixture was studied in situ using neutron diffraction. Neutron diffraction allowed in situ observation of large samples during reduction at high temperatures. Australian hematite ore, studied as a comparison, reduced much more quickly than the pre-oxidised ironsand, which in turn reduced more quickly than raw ironsand. The ironsand was predominantly titanomagnetite with small amounts of titanohematite. The rate of wustite formation increased and metallic iron was formed only after the reduction of titanohematite. Experimental results confirmed the expected reduction pathway for initial reduction of titanomagnetite ore was described well by a three-interface shrinking core model. The rate controlling step in the reduction reactions studied was the mass transport of water vapour in the bulk gas. At higher temperatures, slow removal of water vapour meant that the pH(2)O increased, thus preventing reduction of wustite to metallic iron.
引用
收藏
页码:183 / 192
页数:10
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