Effects Of Cerium On Magnetic Properties Of Sintered R-Fe-B Permanent Magnets
2018 IEEE INTERNATIONAL MAGNETIC CONFERENCE (INTERMAG)(2018)
Abstract
As an element in Lanthanide, Cerium has the highest reserve in global rare earth resources (up to $40 sim 50$ % of total RE). To make the best use of Ce will improve the balance of rare-earth applications. Originating from the mixed valence characteristics of Ce ions in rare-earth transition compounds, its physical and chemical properties usually deviate from the trend of whole RE family. Ce exists in Ce 2 Fe 14 B almost as Ce 4+ ion. The lack of 4f electron leads Ce 4+ to make no contribution to magnetism, especially the magneto-crystalline anisotropy. Small ion radius shrinks the Fe-Fe distances and consequently decreases the exchange interaction of Fe sub-lattice, which makes Ce 2 Fe 14 B have lower Curie temperature $mathrm {T_{C}}$ than other R 2 Fe 14 B compounds. The $mathrm {T_{C}}$ of Ce 2 Fe 14 B is 422 K which is 164 K less than Nd 2 Fe 14 B. J s is 1.17 T, 0.43 T less than Nd 2 Fe 14 B. The anisotropic field $mu _{0} mathrm {H_{a}}$ is 3.6T, only 47% of Nd 2 Fe 14 B. In addition to decreasing the intrinsic magnetic properties in Ce 2 Fe 14 B, Ce also makes heavy damage on the coercivity of sintered Ce-Fe-B magnet. Because the conventional powder metallurgic procedure is in favor of forming CeFe 2 Laves phase instead of Ce-rich phase that magnetically decouple Ce 2 Fe 14 B grains. Even so, Ce 2 Fe 14 B still has comparable J s to that of SmCo 5 and reasonable $mu _{0} mathrm {H_{a}}$ for permanent magnet development. To add La, the RE element with the largest ion radius, is possible to improve the intrinsic magnetic properties of (La x Ce 1-x ) 2 Fe 14 B [1]. The lattice parameters increase linearly with Ce content x which gives $mathrm {a}= 0.8763 +0.0033mathrm {x}($ nm) and $mathrm {c}= 1.2135 +0.0114mathrm {x}($ nm). As a result, $mathrm {T_{C}}$ do increase linearly with $mathrm {T_{C}}= 427.4 +59.0mathrm {x}(mathrm {K})$. Unfortunately the J s at the temperature of 5K do not indicate the same increase with lattice expansion and keeps approximately a constant of 1.51 T. The practical way of preparing Ce-contained permanent magnet is to let Ce replace Nd to its upper limit. Rapidly quenching routine is straight forward to get rid of the necessity of Ce-rich phase. As shown in Fig.1 [2], even though all the permanent magnetic parameters drop linearly with Ce content x, isotropic [(Nd 0.75 Pr 0.25 ) 1-x Ce x ] 11.65 Fe 82.75 B 5.6 powder can still realize reasonable $mathrm {H_{cJ}}$ and $(mathrm{BH)_{max}}$ for certain applications. For example, $mathrm {B_{r}} =8.54$ kG, $mathrm {H_{cJ}} =9.4$ kOe and $(mathrm{BH)_{max}}=14.8$ MGOe when Ce replaces Nd-Pr by 20 at% $(mathrm {x} = 0.2)$. At $mathrm {x}=0.5$, $mathrm {H_{cJ}}$ keeps about 6.8 kOe with $(mathrm{BH)_{max}}$ of 11.6 MGOe. And the B r is 7.82 kG. $mathrm {T_{C}}$ at this composition is reasonably high as 509 K. In preparation of sintered magnets containing Ce, dual-alloy or dual main-phase techniques are usually applied. With Ce-rich/Nd-lean alloy and Nd-rich/Ce-lean alloy as starting materials, sintered (Ce,Nd)-Fe-B magnet is commercialized with high ratio of performance to cost. The key point is to let plenty of Nd-rich phase magnetically decouple (Ce,Nd) 2 Fe 14 B grains. As shown in Table 1 [3], by mixing strip casted Nd-Fe-B and (Ce-Nd)-Fe-B alloy powder with different ratio, the sintered magnet with 45wt% Ce and 55wt% Nd in total rare earth composition gives $mathrm {B_{r}} =12.4$ kG, $mathrm {H_{cJ}}=6.2$ kOe and $(mathrm{BH)_{max}} =33.4$ MGOe. At Ce of 20wt%, the correspondent parameters are 13.7 kG, 12.0 kOe and 45.0 MGOe, which is good enough to many applications. The melting points of R-rich phase decrease with Ce composition. This implies that sintering temperature for high Ce-containing magnet can be lower than low Ce-containing magnet. Another example is to directly use misch-metal (MM) as raw material [4]. The typical composition of MM is La 27.06 wt%, Ce 51.46 wt%, Pr 5.22 wt%, and Nd 16.16 wt%. When MM to total RE ratio is 21.5%, $mathrm {B_{r}}= 12.09$ kG, $mathrm {H_{cJ}}= 10.70$ kOe and $(mathrm{BH)_{max}}= 34.04$ MGOe. For magnet only with MM, $mathrm {H_{cJ}}$ is as low as 0.46 kOe. $(mathrm{BH)_{max}}$ is just 2.40 MGOe. Microstructure observation shows that RFe 2 grains, in which Ce is the main component of R, distribute in triangle junction area formed by neighbor R 2 Fe 14 Bgrains. The lack of inter-granular R-rich phase is responsible for low $mathrm {H_{cJ}}$ in sintered MM-Fe-B magnet.
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Key words
sintered permanent magnets,mixed valence compounds,physical properties,chemical properties,magneto-crystalline anisotropy,exchange interaction,Curie temperature,coercivity,powder metallurgy,lattice parameters,ion radius,lattice expansion,melting points,isotropic powder composition,microstructural behavior,[(Nd0.75Pr0.25)1-xCex]11.65Fe82.75B5.6
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