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All sourcesNASA NTRSDOE OSTI
DOE OSTI2024

Measurements of Born cross sections for e + e − → Λ c + Λ ¯ c ( 2595 ) − + c . c . and e + e − → Λ c + Λ ¯ c ( 2625 ) − + c . c . at s = 4918.0 and 4950.9 MeV

Using e + e − collision data collected with the BESIII detector operating at the BEPCII collider, the Born cross sections of e + e − → Λ c + Λ ¯ c ( 2595 ) − + c . c . and e + e − → Λ c + Λ ¯ c ( 2625 ) − + c . c . are measured for the first time at center-of-mass energies of s = 4918.0 and 4950.9 MeV. Nonzero cross sections are observed very close to the production threshold. The measured Born cross sections of e + e − → Λ c + Λ ¯ c ( 2625 ) − + c . c . are about 2–3 times greater than those of e + e − → Λ c + Λ ¯ c ( 2595 ) − + c . c . , providing the similar behavior as semileptonic decays of Λ b 0 , but different behavior from that in the hadronic decays of Λ b 0 . The Born cross sections are 15.6 ± 3.1 ± 0.9 pb and 29.4 ± 3.7 ± 2.7 pb for e + e − → Λ c + Λ ¯ c ( 2595 ) − + c . c . , and are 43.4 ± 4.0 ± 4.1 pb and 76.8 ± 6.5 ± 4.2 pb for e + e − → Λ c + Λ ¯ c ( 2625 ) − + c . c . at s = 4918.0 and 4950.9 MeV, respectively. Based on the polar angle distributions of the Λ ¯ c ( 2625 ) − and Λ c ( 2625 ) + , the form-factor ratios | G E | 2 + 3 | G M | 2 / | G C | are determined for e + e − → Λ c + Λ ¯ c ( 2625 ) − + c . c . for the first time, which are 5.95 ± 4.07 ± 0.15 and 0.94 ± 0.32 ± 0.02 at s = 4918.0 and 4950.9 MeV, respectively. All of these first uncertainties are statistical and second systematic. Published by the American Physical Society 2024

Astronomy & Astrophysics↗
DOE OSTI2023

Measurements of branching fractions of Λ$^{+}_{c}$ → Σ + ⁢η and Λ$^{+}_{c}$ → Σ + ⁢η' and asymmetry parameters of Λ$^{+}_{c}$ → Σ + ⁢π 0 , Λ$^{+}_{c}$ → Σ + ⁢η, and Λ$^{+}_{c}$ → Σ + ⁢η'

We report a study of Λ c + → Σ + π 0 , Λ c + → Σ + η , and Λ c + → Σ + η ' using the data sample corresponding to an integrated luminosity of 980 fb - 1 collected with the Belle detector at the KEKB asymmetric-energy e + e - collider. The branching fractions relative to Λ c + → Σ + π 0 are measured as B Λ c + → Σ + η / B Λ c + → Σ + π 0 = 0.25 ± 0.03 ± 0.01 and B Λ c + → Σ + η ' / B Λ c + → Σ + π 0 = 0.33 ± 0.06 ± 0.02 . Using B Λ c + → Σ + π 0 = ( 1.25 ± 0.10 ) % , we obtain B Λ c + → Σ + η = ( 3.14 ± 0.35 ± 0.17 ± 0.25 ) × 10 - 3 and B Λ c + → Σ + η ' = ( 4.16 ± 0.75 ± 0.25 ± 0.33 ) × 10 - 3 . Here the uncertainties are statistical, systematic, and from B Λ c + → Σ + π 0 , respectively. The ratio of the branching fraction of Λ c + → Σ + η ' with respect to that of Λ c + → Σ + η is measured to be B Λ c + → Σ + η ' / B Λ c + → Σ + η = 1.34 ± 0.28 ± 0.08 . We update the asymmetry parameter of Λ c + → Σ + π 0 , α Σ + π 0 = - 0.48 ± 0.02 ± 0.02 , with a considerably improved precision. The asymmetry parameters of Λ c + → Σ + η and Λ c + → Σ + η ' are measured to be α Σ + η = - 0.99 ± 0.03 ± 0.05 and α Σ + η ' = - 0.46 ± 0.06 ± 0.03 for the first time.

72 PHYSICS OF ELEMENTARY PARTICLES AND FIELDS↗
DOE OSTI2024

Search for charmed baryons in the Λ c + η system and measurement of the branching fractions of Λ c ( 2880 ) + and Λ c ( 2940 ) + decaying to Λ c + η and p D 0 relative to Σ c ( 2455 ) π

We search for excited charmed baryons in the Λ c + η system using a data sample corresponding to an integrated luminosity of 980 fb − 1 . The data were collected by the Belle detector at the KEKB e + e − asymmetric-energy collider. No significant signals are found in the Λ c + η mass spectrum, including the known Λ c ( 2880 ) + and Λ c ( 2940 ) + . Clear Λ c ( 2880 ) + and Λ c ( 2940 ) + signals are observed in the p D 0 mass spectrum. We set upper limits at 90% credibility level on ratios of branching fractions of Λ c ( 2880 ) + and Λ c ( 2940 ) + decaying to Λ c + η relative to Σ c ( 2455 ) π of < 0.13 for the Λ c ( 2880 ) + and < 1.11 for the Λ c ( 2940 ) + . We measure ratios of branching fractions of Λ c ( 2880 ) + and Λ c ( 2940 ) + decaying to p D 0 relative to Σ c ( 2455 ) π of 0.75 ± 0.03 ( stat ) ± 0.07 ( syst ) for the Λ c ( 2880 ) + and 3.59 ± 0.21 ( stat ) ± 0.56 ( syst ) for the Λ c ( 2940 ) + . Published by the American Physical Society 2024

Astronomy & Astrophysics↗
DOE OSTI2023

Measurement of the mass and width of the Λ c ⁢(2625) + charmed baryon and the branching ratios of Λ c ⁢(2625) + → Σ$^{0}_{c}$π + and Λ c ⁢(2625) + → Σ$^{++}_{c}$π -

Using the entire data sample of 980 fb -1 collected at or near the Y⁡(4⁢S) resonance with the Belle detector operating at the KEKB asymmetric-energy e + ⁢e - collider, we report the measurement of the mass, width, and the branching ratios of the Λ c (2625) + charmed baryon. The mass difference between Λ c ⁢(2625) + and Λ$^{+}_{c}$ is measured to be M⁡(Λ c ⁢(2625) + )-M⁡(Λ$^{+}_{c}$)=341.518±0.006±0.049 MeV/c 2 . The upper limit on the width is measured to be Γ⁡(Λ c ⁢(2625) + )<0.52 MeV/c 2 at 90% confidence level. Based on a full Dalitz plot fit, branching ratios with respect to the mode Λ c⁢ (2625) + →Λ$^{+}_{c}$π + ⁢π - are measured to be $\frac{\mathscr{B}⁡(Λ_c(2625)^+ → Σ^{0}_{c}π^+)} {\mathscr{B}⁡(Λ_c(2625)^+ → ^{+}_{c}⁢π^+⁢π^-)}$ = (5.19±0.23±0.40)% and $\frac{\mathscr{B}(Λ_c (2625)^+ → Σ{_c^+}^+ π^-)}{\mathscr{B}(Λ_c (2625)^+ → Λ{_c^+} π^+π^-)}$ = (5.13±0.26±0.32)%, where the first and second uncertainties are statistical and systematic, respectively. These measurements can be used to further constrain the parameters of the underlying theoretical models.

72 PHYSICS OF ELEMENTARY PARTICLES AND FIELDS↗
DOE OSTI2024

Study of h c → 3 ( π + π − ) π 0 , h c → 2 ( π + π − ) ω , h c → 2 ( π + π − ) π 0 η , h c → 2 ( π + π − ) η , and h c → p p ¯

Based on ( 2712.4 ± 14.1 ) × 10 6 ψ ( 3686 ) events collected with the BESIII detector, we study the decays h c → 3 ( π + π − ) π 0 , h c → 2 ( π + π − ) ω , h c → 2 ( π + π − ) π 0 η , h c → 2 ( π + π − ) η , and h c → p p ¯ via ψ ( 3686 ) → π 0 h c . The decay channel h c → 3 ( π + π − ) π 0 is observed for the first time, and its branching fraction is determined to be ( 9.28 ± 1.14 ± 0.77 ) × 10 − 3 , where the first uncertainty is statistical and the second is systematic. In addition, first evidence is found for the modes h c → 2 ( π + π − ) π 0 η and h c → 2 ( π + π − ) ω with significances of 4.8 σ and 4.7 σ , and their branching fractions are determined to be ( 7.55 ± 1.51 ± 0.77 ) × 10 − 3 and ( 4.00 ± 0.86 ± 0.35 ) × 10 − 3 , respectively. No significant signals of h c → 2 ( π + π − ) η and h c → p p ¯ are observed, and the upper limits of the branching fractions of these decays are determined to be < 6.19 × 10 − 4 and < 4.40 × 10 − 5 at the 90% confidence level, respectively. Published by the American Physical Society 2024

Astronomy & Astrophysics↗
DOE OSTI2022

Concurrent Precipitation of Nb(C,N) and Metastable M 23 C 6 in Alloy 347H at 700°C and 750°C: Computer Simulations and Comparison to Experiment

Here, we present our results for the concurrent precipitation of metastable M 23 C 6 , Nb(C,N) secondary precipitates, and the Nb(C,N) primary crystals in 347H austenitic stainless steel. For precipitation modeling, we have accounted for the elastic contribution to interfacial energy, and for the Fe-spin-polarization for NbC/Fe and M 23 C 6 /Fe interfacial energy values: for NbC/Fe ~ 0.63 J/m 2 . For M 23 C 6 precipitates, an error function was used to describe the interfacial energy growth with particle size. In precipitation simulations, the average size of the primary Nb(C,N) particles remained ~ 1 μm at 700°C and ~ 0.3 μm at 750°C. The M 23 C 6 precipitates at 750°C dissolved after 120 h (our simulations) compared to 300 h (experiments). The Nb(C,N)/Fe interfacial energy was not affected by the nitrogen additions. With these modifications, reasonable agreement with the available experimental data was obtained, which allows using them in the development of the 2nd-phase particle-informed creep theory.

36 MATERIALS SCIENCE↗
DOE OSTI2022

Modification of conventional peak shapes to accurately represent spectral asymmetry: High-Resolution X-ray photoelectron spectra of [C 4 C 1 Pyrr][NTf 2 ] and [C 8 C 1 Im][NTf 2 ] ionic liquids

X-ray photoelectron spectroscopy (XPS) is one of the most widely used techniques for surface characterization. Analysis of XPS data is challenging and requires the analyst to fit the data with synthetic line shapes to reach physically meaningful interpretations. Experimental spectral envelopes, however, are complex and display asymmetric features that are often ignored or attributed to additional chemical components. The high-resolution XPS spectra of [C 4 C 1 Pyrr][NTf 2 ] and [C 8 C 1 Im][NTf 2 ] all exhibit a degree of asymmetry which is systematically observed at the higher binding energy side of photoemission envelopes. Here, we present the development of a refined fitting procedure for XPS spectra of these ionic liquid-based systems which include (a) Shirley background offset necessary to account for the insulator-like region and (b) spectral asymmetry in C 1s and N 1s regions. Further, Shirley and trapezoid components are applied to compensate for inelastic scattering taking place during electron transitions as high as 7.8 eV above the start of the fitting region in C 1s high-resolution spectrum. To demonstrate the fitness of this model, we present an analysis of a 2:1 mixture of [C 4 C 1 Pyrr][NTf 2 ]: [C 8 C 1 Im][NTf 2 ].

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2023

Is the polarization of the C$=$C bond imperative for bifunctional outer-sphere C$=$C hydrogenation?

Understanding controlling factors is important for the development of bifunctional outer-sphere C$=$C hydrogenations. In this study, a dominant view is that the polarization of C$=$C bonds is imperative for these reactions. However, the present comparative DFT study suggests that the polarization of C$=$C bonds is not the controlling factor. Instead, the “push–pull” type π-conjugative effect can decrease activation barriers and contribute to outer-sphere bifunctional C$=$C bond hydrogenations. What is more, this study shows the feasibility of the asymmetric bifunctional outer-sphere C$=$C hydrogenation.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2022

Low temperature catalytic conversion of CH 4 , CO 2 , and C 2 H 4 to value-added C 3 oxygenates and olefins via C 1 -C 2 coupling on Pd-Au/CeO 2

The catalytic conversion of CH 4 and CO 2 in the presence of more reactive co-reactants C 2 H 4 and O 2 on Pd-Au/CeO 2 is achieved at 200 °C and elevated pressures. Propene and acetone were produced from the catalyzed reaction of CH 4 +C 2 H 4 +O 2 ; addition of CO 2 to the reactant stream produced methyl acetate (MAc) but it significantly reduced the C-selectivities of propene and acetone. DRIFTS experiments confirmed the formation of methoxy species from CH 4 +CO 2 at 200 °C, which is an intermediate in the formation of MAc. Here, control experiments with blanks, and with CeO 2 did not show any propene, acetone, or MAc products. The complete oxidation of C 2 H 4 was avoided; the catalyst is stable, and reactant conversions and product yields were sustained for the observed 1200 min time-on-stream, indicating that there is little or no carbon deposition and sintering. This direct coupling of CH 4 and C 2 H 4 intermediates to higher carbon-number products at 200 °C is significant.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2024

First measurements of the absolute branching fraction of Λ c ( 2625 ) + → Λ c + π + π − and upper limit on Λ c ( 2595 ) + → Λ c + π + π −

The absolute branching fraction of the decay Λ c ( 2625 ) + → Λ c + π + π − is measured for the first time to be ( 50.2 ± 5.7 stat ± 3.5 syst ) % with 368.48 pb − 1 of e + e − collision data collected by the BESIII detector at the center-of-mass energies of s = 4.918 and 4.950 GeV. Although the central value of the result is lower than the theoretical prediction of 67%, obtained from isospin symmetry, they are consistent taking the uncertainties into account. This is the first absolute branching fraction measurement for Λ c ( 2625 ) + since it was found. This measurement is necessary to obtain the coupling constants for the transitions between s -wave and p -wave charmed baryons in heavy hadron chiral perturbation theory. In addition, we search for the decay Λ c ( 2595 ) + → Λ c + π + π − . No significant signal is observed, and the upper limit on its branching fraction is determined to be 85.0% at the 90% confidence level. Published by the American Physical Society 2024

Astronomy & Astrophysics↗
DOE OSTI2024

Observation of χ c J → p p ¯ K S 0 K − π + + c . c .

By analyzing ( 27.12 ± 0.14 ) × 10 8 ψ ( 3686 ) events collected with the BESIII detector operating at the BEPCII collider, the decays χ c J → p p ¯ K S 0 K − π + + c . c . ( J = 0 , 1 , 2 ) are observed for the first time with statistical significances greater than 10 σ . The branching fractions of these decays are determined to be B ( χ c 0 → p p ¯ K S 0 K − π + + c . c . ) = ( 2.61 ± 0.27 ± 0.32 ) × 10 − 5 , B ( χ c 1 → p p ¯ K S 0 K − π + + c . c . ) = ( 4.16 ± 0.24 ± 0.46 ) × 10 − 5 , and B ( χ c 2 → p p ¯ K S 0 K − π + + c . c . ) = ( 5.63 ± 0.28 ± 0.46 ) × 10 − 5 , respectively. The processes χ c 1 , 2 → p ¯ Λ ( 1520 ) K S 0 π + + c . c . are also observed, with statistical significances of 5.7 σ and 7.0 σ , respectively. Evidence for χ c 0 → p ¯ Λ ( 1520 ) K S 0 π + + c . c . is found with statistical significances of 3.3 σ . The corresponding branching fractions are determined to be B ( χ c 0 → p ¯ Λ ( 1520 ) K S 0 π + + c . c . ) = ( 1.6 1 − 0.64 + 0.68 ± 0.23 ) × 10 − 5 , B ( χ c 1 → p ¯ Λ ( 1520 ) K S 0 π + + c . c . ) = ( 4.06 − 0.76 + 0.80 ± 0.52 ) × 10 − 5 , and B ( χ c 2 → p ¯ Λ ( 1520 ) K S 0 π + + c . c . ) = ( 4.0 9 − 0.84 + 0.87 ± 0.42 ) × 10 − 5 . Here, the first uncertainties are statistical and the second ones are systematic. Published by the American Physical Society 2024

Ablikim, M.↗
DOE OSTI2022

A crossed molecular beams and computational study on the unusual reactivity of banana bonds of cyclopropane (c-C 3 H 6 ; X 1 A$^{'}_{1}$ ) through insertion by ground state carbon atoms (C( 3 P j ))

The mechanism and chemical dynamics of the reaction of ground electronic state atomic carbon C( 3 P j ) with cyclopropane c-C 3 H 6 (X 1 A$^{'}_{1}$) have been explored by combining crossed molecular beams experiments with electronic structure calculations of the pertinent triplet C 4 H 6 potential energy surface and statistical computations of product branching ratios under single-collision conditions. The experimental findings suggest that the reaction proceeds via indirect scattering dynamics through triplet C 4 H 6 reaction intermediate(s) leading to C 4 H 5 product(s) plus atomic hydrogen via a tight exit transition state, with the overall reaction exoergicity evaluated as 231 ± 52 kJ mol –1 . The calculations indicate that C( 3 P j ) can easily insert into one of the three equivalent C–C ‘banana’ bonds of cyclopropane overcoming a low barrier of only 2 kJ mol –1 following the formation of a van der Waals reactant complex stabilized by 15 kJ mol –1 . The carbon atom insertion into one of the six C–H bonds is also feasible via a slightly higher barrier of 5 kJ mol –1 . Here, these results highlight an unusual reactivity of cyclopropane's banana C–C bonds, which behave more like unsaturated C–C bonds with a π-character than saturated σ C–C bonds, which are known to be generally unreactive toward the ground electronic state atomic carbon such as in ethane (C 2 H 6 ). The statistical theory predicts the overall product branching ratios at the experimental collision energy as 50% for 1-butyn-4-yl, 33% for 1,3-butadien-2-yl, i-C 4 H 5 , and 11% for 1,3-butadien-1-yl, n-C 4 H 5 , with i-C 4 H 5 (230 kJ mol –1 below the reactants) favored by the C–C insertion providing the best match with the experimentally observed reaction exoergicity. The C( 3 P j ) + c-C 3 H 6 reaction is predicted to be a source of C 4 H 5 radicals under the conditions where its low entrance barriers can be overcome, such as in planetary atmospheres or in circumstellar envelopes but not in cold molecular clouds. Both i- and n-C 4 H 5 can further react with acetylene eventually producing the first aromatic ring and hence, the reaction of the atomic carbon with c-C 3 H 6 can be considered as an initial step toward the formation of benzene.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2025

Measurements of the branching fractions of ${\Xi }_{c}^{+}\to {\Sigma }^{+}{K}_{S}^{0}$, ${\Xi }_{c}^{+}\to {\Xi }^{0}{\pi }^{+}$, and ${\Xi }_{c}^{+}\to {\Xi }^{0}{K}+$ at Belle and Belle II

Using 983.0 fb −1 and 427.9 fb −1 data samples collected with the Belle and Belle II detectors at the KEKB and SuperKEKB asymmetric energy e + e − colliders, respectively, we present studies of the Cabibbo-favored ${\Xi }_{c}^{+}$ decays ${\Xi }_{c}^{+}\to {\Sigma }^{+}{K}_{S}^{0}$ and ${\Xi }_{c}^{+}\to {\Xi }^{0}{\pi }^{+}$, and the singly Cabibbo-suppressed decay ${\Xi }_{c}^{+}\to {\Xi }^{0}{K}^{+}$. The ratios of branching fractions of ${\Xi }_{c}^{+}\to {\Sigma }^{+}{K}_{S}^{0}$ and ${\Xi }_{c}^{+}\to {\Xi }^{0}{K}^{+}$ relative to that of ${\Xi }_{c}^{+}\to {\Xi }^{-}{\pi }^{+}{\pi }^{+}$ are measured for the first time, while the ratio $\mathcal{B}({\Xi }_{c}^{+}\to {\Xi }^{0}{\pi }^{+})/\mathcal{B}({\Xi }_{c}^{+}\to {\Xi }^{-}{\pi }^{+}{\pi }^{+})$ is also determined and improved by an order of magnitude in precision. The measured branching fraction ratios are $\begin{array}{c}\frac{\mathcal{B}\left({\Xi }_{c}^{+}\to {\Sigma }^{+}{K}_{S}^{0}\right)}{\mathcal{B}\left({\Xi }_{c}^{+}\to {\Xi }^{-}{\pi }^{+}{\pi }^{+}\right)}=0.067\pm 0.007\pm 0.003,\\ \frac{\mathcal{B}\left({\Xi }_{c}^{+}\to {\Xi }^{0}{\pi }^{+}\right)}{\mathcal{B}\left({\Xi }_{c}^{+}\to {\Xi }^{-}{\pi }^{+}{\pi }^{+}\right)}=0.251\pm 0.005\pm 0.010,\\ \frac{\mathcal{B}\left({\Xi }_{c}^{+}\to {\Xi }^{0}{K}^{+}\right)}{\mathcal{B}\left({\Xi }_{c}^{+}\to {\Xi }^{-}{\pi }^{+}{\pi }^{+}\right)}=0.017\pm 0.003\pm 0.001.\end{array}$ Additionally, the ratio $\mathcal{B}({\Xi }_{c}^{+}\to {\Xi }^{0}{K}^{+})/\mathcal{B}({\Xi }_{c}^{+}\to {\Xi }^{0}{\pi }^{+})$ is measured to be 0.068 ± 0.010 ± 0.004. Here, the first and second uncertainties are statistical and systematic, respectively. Multiplying the ratios by the branching fraction of the normalization mode, $\mathcal{B}({\Xi }_{c}^{+}\to {\Xi }^{-}{\pi }^{+}{\pi }^{+})=(2.9\pm 1.3)%$, we obtain the following absolute branching fractions $\begin{array}{c}\mathcal{B}({\Xi }_{c}^{+}\to {\Sigma }^{+}{K}_{S}^{0})=(0.194\pm 0.021\pm 0.009\pm 0.087)\text{%},\\ \mathcal{B}({\Xi }_{c}^{+}\to {\Xi }^{0}{\pi }^{+})=(0.728\pm 0.014\pm 0.027\pm 0.326)\text{%},\\ \mathcal{B}({\Xi }_{c}^{+}\to {\Xi }^{0}{K}^{+})=(0.049\pm 0.007\pm 0.003\pm 0.022)\text{%},\end{array}$ where the third uncertainties are from $\mathcal{B}({\Xi }_{c}^{+}\to {\Xi }^{-}{\pi }^{+}{\pi }^{+})$.

72 PHYSICS OF ELEMENTARY PARTICLES AND FIELDS↗
DOE OSTI2022

Asymmetrical C–C Coupling for Electroreduction of CO on Bimetallic Cu–Pd Catalysts

Electroreduction of carbon monoxide (CO) possesses great potential for achieving the renewable synthesis of hydrocarbon chemicals from CO 2 . We report here selective reduction of CO to acetate using Cu–Pd bimetallic electrocatalysts. High activity and selectivity are demonstrated for CO-to-acetate conversion with >200 mA/cm 2 in geometric current density and >65% in Faradaic efficiency (FE). An asymmetrical C–C coupling mechanism is proposed to explain the composition-dependent catalytic performance and high selectivity toward acetate. This mechanism is supported by the computationally predicted shift of the *CO adsorption from the top-site configuration on Cu (or Cu-rich) surfaces to the bridge sites of Cu–Pd bimetallic surfaces, which is also associated with the reduction of the CO hydrogenation barrier. Further kinetic analysis of the reaction order with respect to CO and Tafel slope supports a reaction pathway with *CO–*CHO recombination following a CO hydrogenation step, which could account for the electroreduction of CO to acetate on the Cu–Pd bimetallic catalysts. Furthermore, our work highlights how heteroatomic alloy surfaces can be tailored to enable distinct reaction pathways and achieve advanced catalytic performance beyond monometallic catalysts.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2023

Simultaneous removal of C 2 H 2 and C 2 H 6 for C 2 H 4 purification by robust MOFs featuring a high density of heteroatoms

Simultaneous removal of C 2 H 6 and C 2 H 2 from C 2 H 4 streams is of great importance in the petrochemical industry but remains a challenging task. To address this challenge, we have selected three isoreticular MOFs with high stability, low cost, and desirable scale-up ability, namely, MOF-303, MIL-160, and CAU-23 and assessed their potential in simultaneous removal of acetylene and ethane for ethylene purification. Each MOF exhibits desirable C 2 H 2 and C 2 H 6 uptake capacity (>5.5 mmol g –1 and >4 mmol g –1 , respectively), as well as good C 2 H 2 /C 2 H 4 selectivity (>2) and C 2 H 6 /C 2 H 4 selectivity (>1.5). Notably, MOF-303 takes up 4.96 mmol g –1 C 2 H 6 at 298 K and 1 bar, the highest value among the three MOFs, with C 2 H 6 /C 2 H 4 selectivity in the range of 1.55–2.47. MIL-160 possesses a very high C 2 H 2 uptake (9.1 mmol g –1 ) and C 2 H 2 /C 2 H 4 selectivity, 10.6 (1 : 1, v/v), at 298 K, much higher than those of all other MOFs tested to date for simultaneous removal of C 2 H 6 and C 2 H 2 from C 2 H 4 . The results from breakthrough experiments confirm that all three MOFs demonstrate excellent performance for C 2 H 4 purification in a ternary mixture of C 2 H 6 /C 2 H 4 /C 2 H 2 (1 : 1 : 1, v/v/v). Here, for MOF-303, MIL-160, and CAU-23, polymer-grade C 2 H 4 up to 0.164, 0.21, and 0.181 mmol g –1 can be obtained from the equimolar ternary mixture in a single separation step from the breakthrough experiment. Additionally, DFT calculations have been performed to further investigate the mechanism of adsorption/separation for C 2 H 6 , C 2 H 4 , and C 2 H 2 .

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2024

Search for η c ( 2 S ) → π + π − η c and η c ( 2 S ) → π + π − K S 0 K ± π ∓ decays

Based on ( 27.12 ± 0.14 ) × 10 8 ψ ( 2 S ) events collected by the BESIII detector, we search for the decay η c ( 2 S ) → π + π − η c via ψ ( 2 S ) → γ η c ( 2 S ) . No significant signal is observed, and the upper limit on the product branching fraction B ( ψ ( 2 S ) → γ η c ( 2 S ) ) × B ( η c ( 2 S ) → π + π − η c ) is determined to be 2.21 × 10 − 5 at the 90% confidence level. In addition, the η c ( 2 S ) → π + π − K S 0 K ± π ∓ decay is studied via ψ ( 2 S ) → γ η c ( 2 S ) and is observed with a statistical significance of 10 σ for the first time. The branching fraction of η c ( 2 S ) → π + π − K S 0 K ± π ∓ is determined to be ( 1.33 ± 0.11 ± 0.40 ± 0.95 ) × 10 − 2 , where the first uncertainty is statistical, the second is systematic, and the third uncertainty is due to the quoted B ( ψ ( 2 S ) → γ η c ( 2 S ) ) . Published by the American Physical Society 2024

Astronomy & Astrophysics↗