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DOE OSTI2025

$Ξ$ 𝑐 → $Ξ$ form factors from lattice QCD with domain-wall quarks: A new piece in the puzzle of $Ξ^0_𝑐$ decay rates

We present a lattice quantum chromodynamics (QCD) determination of the vector and axial-vector form factors that describe the charm-baryon semileptonic decays Ξ 𝑐 → Ξ⁢ℓ + ⁢𝜈 ℓ . The calculation uses a domain-wall action for the up, down, and strange quarks, and an anisotropic clover action for the charm quark. We use four ensembles of gauge-field configurations generated by the RBC and UKQCD collaborations, with lattice spacings between 0.111 and 0.073 fm and pion masses ranging from 420 to 230 MeV. We present Standard Model predictions for the decay rates and branching fractions of Ξ$^0_𝑐$ → Ξ$^−_𝑐$⁢ℓ + ⁢𝜈 ℓ and Ξ$^+_𝑐$ → Ξ$^0_𝑐$⁢ℓ + ⁢𝜈 ℓ for ℓ =𝑒, 𝜇. In particular, we obtain Γ⁡(Ξ$^0_𝑐$ → Ξ − ⁢𝑒 + ⁢𝜈 𝑒 )/|𝑉 𝑐⁢𝑠 | 2 = 0.2515⁢(73) ps −1 and ℬ⁡(Ξ$^0_𝑐$ → Ξ − ⁢𝑒 +⁢ 𝜈 𝑒 ) = 3.58⁢(12)%. These values are higher than those predicted by a previous lattice calculation and substantially higher than the experimentally measured values, but consistent with expectations from approximate 𝑆⁢𝑈⁡(3) flavor symmetry.

72 PHYSICS OF ELEMENTARY PARTICLES AND FIELDS↗

DOE OSTI2024

An electrochemical generator for the continual supply of 213 Bi from 225 Ac for use in targeted alpha therapy applications

Bismuth-213 is a radionuclide of interest for targeted alpha therapy and is supplied via a radiochemical generator system through the decay of 225 Ac. Radionuclide generators employ longer lived “parent” radionuclides to routinely supply shorter-lived “daughter” radionuclides. The traditional 225 Ac/ 213 Bi radiochemical generator relies on an organic cation exchange resin where 225 Ac binds to the resin and 213 Bi is routinely eluted. These resins degrade when they absorb large doses of ionizing radiation (>1 × 10 6 Gy/mg), which has been observed when the loading activity of 225 Ac exceeds 2.59*10 9 Bq (70 mCi). Herein we report the development of an electrochemical generator for the supply of 213Bi that has the potential to overcome this limitation. Bismuth-213 spontaneously electrodeposits onto nickel foils in 0.1 M hydrochloric acid at 70 °C. Using this method, we were able to plate an average of 73 ± 4 % of the 213 Bi in solution and obtain a final 213 Bi recovery of 65 ± 8 % in 0.1 M citrate pH 4.5 via reverse electrolysis using titanium as the cathode. The recovered 213Bi had an average radiochemical purity of >99.8 % and was successfully used to radiolabel DOTATATE with an average radiochemical yield of 85.1 % (not optimized).

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗