TY - JOUR
T1 - U-Pt-Sm-Ba-O chemical pinning centers in Ag-doped Sm123 textured in reduced oxygen
AU - Sawh, Ravi Persad
AU - Weinstein, Roy
AU - Parks, Drew
AU - Chikumoto, Noriko
AU - Murakami, Masato
N1 - Funding Information:
Manuscript received August 5, 2002. This work was supported in part by the U.S. Army Research Office, the Welch Foundation, and the State of Texas via the Texas Center for Superconductivity and Advanced Materials (TCSAM). The New Energy and Industrial Technology Development Organization (NEDO) of Japan also supports this work as a Collaborative Research and Development of Fundamental Technologies for Superconductivity Applications.
PY - 2003/6
Y1 - 2003/6
N2 - In the U/n process enriched uranium is admixed to HTS powders, textured and then irradiated with thermal neutrons. Neutrons must penetrate several centimeters for such processing to be successful in textured materials. Bulk Sm123 cannot be U/n processed because thermal neutrons penetrate <1 mm. However, textured Sm123 can still benefit from chemical pinning centers that are formed during U/n processing. Thin or thick films of Sm123 can still be successfully U/n processed. In the present work, powders containing Ag2O + 20 mol% Sm211 + Sm123 + Pt are doped with depleted U, and textured in a 1% oxygen atmosphere. Microstructure studies indicate the presence of small deposits of (U0.5Pt0.5)SmBa2O6, which are double perovskites. Important characteristics of the U-Pt-Sm-Ba-O particles are: (a) average size is 500 nm, (b) distribution is fairly uniform within the Sm123, (c) the number of deposits is proportional to the mass of admixed U (i.e., size is constant for increasing doping levels) (d) U does not substitute into the background Sm123, (e) Ag does not interact with either U or Pt, and (f) there is less coarsening of the U-rich particles when the dwell time of the maximum temperature in the temperature versus time profile is <2 hours. The U-Pt-Sm-Ba-O deposits are strikingly similar to the U-Pt-Y-Ba-O deposits found earlier in U-doped Y123. Tungsten or molybdenum can be used as nonradioactive substitutes for uranium to produce similar double perovskites deposits.
AB - In the U/n process enriched uranium is admixed to HTS powders, textured and then irradiated with thermal neutrons. Neutrons must penetrate several centimeters for such processing to be successful in textured materials. Bulk Sm123 cannot be U/n processed because thermal neutrons penetrate <1 mm. However, textured Sm123 can still benefit from chemical pinning centers that are formed during U/n processing. Thin or thick films of Sm123 can still be successfully U/n processed. In the present work, powders containing Ag2O + 20 mol% Sm211 + Sm123 + Pt are doped with depleted U, and textured in a 1% oxygen atmosphere. Microstructure studies indicate the presence of small deposits of (U0.5Pt0.5)SmBa2O6, which are double perovskites. Important characteristics of the U-Pt-Sm-Ba-O particles are: (a) average size is 500 nm, (b) distribution is fairly uniform within the Sm123, (c) the number of deposits is proportional to the mass of admixed U (i.e., size is constant for increasing doping levels) (d) U does not substitute into the background Sm123, (e) Ag does not interact with either U or Pt, and (f) there is less coarsening of the U-rich particles when the dwell time of the maximum temperature in the temperature versus time profile is <2 hours. The U-Pt-Sm-Ba-O deposits are strikingly similar to the U-Pt-Y-Ba-O deposits found earlier in U-doped Y123. Tungsten or molybdenum can be used as nonradioactive substitutes for uranium to produce similar double perovskites deposits.
KW - Critical current density
KW - High-temperature superconductors
KW - Melt-textured Sm123
KW - Pinning centers
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U2 - 10.1109/TASC.2003.812127
DO - 10.1109/TASC.2003.812127
M3 - Conference article
AN - SCOPUS:0042466446
SN - 1051-8223
VL - 13
SP - 3151
EP - 3154
JO - IEEE Transactions on Applied Superconductivity
JF - IEEE Transactions on Applied Superconductivity
IS - 2 III
T2 - 2002 Applied Superconductivity Conference
Y2 - 4 August 2002 through 9 August 2002
ER -