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1. High‑precision measurements of half‐lives for 69Ge, 73Se, 83Sr, 85mSr, and 63Zn radionuclides relevant to the astrophysical p‑process via photoactivation at the Madison Accelerator Laboratory

   https://doi.org/https://link.springer.com/article/10.1007/s10967-020-07589-5  

   Hain, T. A ; Pendleton, S. J. ; Silano, S. A. ; Banu, A. ( December 2020 , Journal of radioanalytical and nuclear chemistry an international journal dealing with all aspects and applications of nuclear chemistry)

   null (Ed.)

   The ground state half-lives of 69Ge, 73Se, 83Sr, 63Zn, and the half-life of the 1/2− isomer in 85Sr have been measured with high precision using the photoactivation technique at an unconventional bremsstrahlung facility that features a repurposed medical electron linear accelerator. The γ-ray activity was counted over about 6 half-lives with a high-purity germanium detector, enclosed into an ultra low-background lead shield. The measured half-lives are: T1/2(69Ge) = 38.82 ± 0.07 (stat) ± 0.06 (sys)h; T1/2(73Se) = 7.18 ± 0.02 (stat) ± 0.004 (sys) h; T1/2(83Sr) = 31.87 ± 1.16 (stat) ± 0.42 (sys) h; T1/2(85mSr) = 68.24 ± 0.84(stat) ± 0.11 (sys) min; T1/2(63Zn) = 38.71 ± 0.25 (stat) ± 0.10 (sys) min. These high-precision half-life measurements will contribute to a more accurate determination of corresponding ground-state photoneutron reaction rates, which are part of a broader effort of constraining statistical nuclear models needed to calculate stellar nuclear reaction rates relevant for the astrophysical p-process nucleosynthesis. 

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2. Measuring the β-decay Properties of Neutron-rich Exotic Pm, Sm, Eu, and Gd Isotopes to Constrain the Nucleosynthesis Yields in the Rare-earth Region

   https://doi.org/10.3847/1538-4357/ac80fc  

   Kiss, G. G. ; Vitéz-Sveiczer, A. ; Saito, Y. ; Tarifeño-Saldivia, A. ; Pallas, M. ; Tain, J. L. ; Dillmann, I. ; Agramunt, J. ; Algora, A. ; Domingo-Pardo, C. ; et al ( September 2022 , The Astrophysical Journal)

   Theβ-delayed neutron-emission probabilities of 28 exotic neutron-rich isotopes of Pm, Sm, Eu, and Gd were measured for the first time at RIKEN Nishina Center using the Advanced Implantation Detector Array (AIDA) and the BRIKEN neutron detector array. The existingβ-decay half-life (T_1/2) database was significantly increased toward more neutron-rich isotopes, and uncertainties for previously measured values were decreased. The new data not only constrain the theoretical predictions of half-lives andβ-delayed neutron-emission probabilities, but also allow for probing the mechanisms of formation of the high-mass wing of the rare-earth peak located atA≈ 160 in ther-process abundance distribution through astrophysical reaction network calculations. An uncertainty quantification of the calculated abundance patterns with the new data shows a reduction of the uncertainty in the rare-earth peak region. The newly introduced variance-based sensitivity analysis method offers valuable insight into the influence of important nuclear physics inputs on the calculated abundance patterns. The analysis has identified the half-lives of¹⁶⁸Sm and of several gadolinium isotopes as some of the key variables among the current experimental data to understand the remaining abundance uncertainty atA= 167–172.

    

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3. 3D1D hydro-nucleosynthesis simulations – I. Advective–reactive post-processing method and its application to H ingestion into He-shell flash convection in rapidly accreting white dwarfs

   https://doi.org/10.1093/mnras/stab500  

   Stephens, David ; Herwig, Falk ; Woodward, Paul ; Denissenkov, Pavel ; Andrassy, Robert ; Mao, Huaqing ( April 2021 , Monthly Notices of the Royal Astronomical Society)

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   ABSTRACT We present two mixing models for post-processing of 3D hydrodynamic simulations applied to convective–reactive i-process nucleosynthesis in a rapidly accreting white dwarf (RAWD) with [Fe/H] = −2.6, in which H is ingested into a convective He shell. A 1D advective two-stream model adopts physically motivated radial and horizontal mixing coefficients constrained by 3D hydrodynamic simulations. A simpler approach uses diffusion coefficients calculated from the same simulations. All 3D simulations include the energy feedback of the 12C(p, γ)13N reaction from the H entrainment. Global oscillations of shell H ingestion in two of the RAWD simulations cause bursts of entrainment of H and non-radial hydrodynamic feedback. With the same nuclear network as in the 3D simulations, the 1D advective two-stream model reproduces the rate and location of the H burning within the He shell closely matching the 3D simulation predictions, as well as qualitatively displaying the asymmetry of the XH profiles between the upstream and downstream. With a full i-process network the advective mixing model captures the difference in the n-capture nucleosynthesis in the upstream and downstream. For example, 89Kr and 90Kr with half-lives of $3.18\,\,\mathrm{\mathrm{min}}$ and $32.3\,\,\mathrm{\mathrm{s}}$ differ by a factor 2–10 in the two streams. In this particular application the diffusion approach provides globally the same abundance distribution as the advective two-stream mixing model. The resulting i-process yields are in excellent agreement with observations of the exemplary CEMP-r/s star CS31062-050. 

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4. Cross-conjugation controls the stabilities and photophysical properties of heteroazoarene photoswitches

   https://doi.org/10.1039/d1ob02026a  

   Adrion, Daniel M. ; Lopez, Steven A. ( January 2022 , Organic & Biomolecular Chemistry)

   Azoarene photoswitches are versatile molecules that interconvert from their E-isomer to their Z-isomer with light. Azobenzene is a prototypical photoswitch but its derivatives can be poorly suited for in vivo applications such as photopharmacology due to undesired photochemical reactions promoted by ultraviolet light and the relatively short half-life (t1/2) of the Z-isomer (2 days). Experimental and computational studies suggest that these properties (λmax of the E isomer and t1/2 of the Z-isomer) are inversely related. We identified isomeric azobisthiophenes and azobisfurans from a high-throughput screening study of 1540 azoarenes as photoswitch candidates with improved λmax and t1/2 values relative to azobenzene. We used density functional theory to predict the activation free energies and vertical excitation energies of the E- and Z-isomers of 2,2- and 3,3-substituted azobisthiophenes and azobisfurans. The half-lives depend on whether the heterocycles are π-conjugated or cross-conjugated with the diazo π-bond. The 2,2-substituted azoarenes both have t1/2 values on the scale of 1 hour, while the 3,3-analogues have computed half-lives of 40 and 230 years (thiophene and furan, respectively). The 2,2-substituted heteroazoarenes have significantly higher λmax absorptions than their 3,3-substituted analogues: 76 nm for azofuran and 77 nm for azothiophene. 

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5. Carbon–titanium dioxide (C/TiO 2 ) nanofiber composites for chemical oxidation of emerging organic contaminants in reactive filtration applications

   https://doi.org/10.1039/D0EN00975J  

   Greenstein, Katherine E. ; Nagorzanski, Matthew R. ; Kelsay, Bailey ; Verdugo, Edgard M. ; Myung, Nosang V. ; Parkin, Gene F. ; Cwiertny, David M. ( March 2021 , Environmental Science: Nano)

   null (Ed.)

   The recalcitrance of some emerging organic contaminants through conventional water treatment systems may necessitate advanced technologies that use highly reactive, non-specific hydroxyl radicals. Here, polyacrylonitrile (PAN) nanofibers with embedded titanium dioxide (TiO 2 ) nanoparticles were synthesized via electrospinning and subsequently carbonized to produce mechanically stable carbon/TiO 2 (C/TiO 2 ) nanofiber composite filters. Nanofiber composites were optimized for reactivity in flow through treatment systems by varying their mass loading of TiO 2 , adding phthalic acid (PTA) as a dispersing agent for nanoparticles in electrospinning sol gels, comparing different types of commercially available TiO 2 nanoparticles (Aeroxide® P25 and 5 nm anatase nanoparticles) and through functionalization with gold (Au/TiO 2 ) as a co-catalyst. High bulk and surface TiO 2 concentrations correspond with enhanced nanofiber reactivity, while PTA as a dispersant makes it possible to fabricate materials at very high P25 loadings (∼80% wt%). The optimal composite formulation (50 wt% P25 with 2.5 wt% PTA) combining high reactivity and material stability was then tested across a range of variables relevant to filtration applications including filter thickness (300–1800 μm), permeate flux (from 540–2700 L m −2 h), incident light energy (UV-254 and simulated sunlight), flow configuration (dead-end and cross-flow filtration), presence of potentially interfering co-solutes (dissolved organic matter and carbonate alkalinity), and across a suite of eight organic micropollutants (atrazine, benzotriazole, caffeine, carbamazepine, DEET, metoprolol, naproxen, and sulfamethoxazole). During cross-flow recirculation under UV-irradiation, 300 μm thick filters (30 mg total mass) produced micropollutant half-lives ∼45 min, with 40–90% removal (from an initial 0.5 μM concentration) in a single pass through the filter. The initial reaction rate coefficients of micropollutant transformation did not clearly correlate with reported second order rate coefficients for reaction with hydroxyl radical ( k OH ), implying that processes other than reaction with photogenerated hydroxyl radical ( e.g. , surface sorption) may control the overall rate of transformation. The materials developed herein represent a promising next-generation filtration technology that integrates photocatalytic activity in a robust platform for nanomaterial-enabled water treatment. 

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