This Letter presents the first experimental evidence of the attractive strong interaction between a proton and a ϕ meson. The result is obtained from two-particle correlations of combined p-ϕ⊕ p[over ¯]-ϕ pairs measured in high-multiplicity pp collisions at sqrt[s]=13 TeV by the ALICE Collaboration. The spin-averaged scattering length and effective range of the p-ϕ interaction are extracted from the fully corrected correlation function employing the Lednický-Lyuboshits approach. In particular, the imaginary part of the scattering length vanishes within uncertainties, indicating that inelastic processes do not play a prominent role for the p-ϕ interaction. These data demonstrate that the interaction is dominated by elastic p-ϕ scattering. Furthermore, an analysis employing phenomenological Gaussian- and Yukawa-type potentials is conducted. Under the assumption of the latter, the N-ϕ coupling constant is found to be g_{N-ϕ}=0.14±0.03(stat)±0.02(syst). This work provides valuable experimental input to accomplish a self-consistent description of the N-ϕ interaction, which is particularly relevant for the more fundamental studies on partial restoration of chiral symmetry in nuclear medium.
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http://dx.doi.org/10.1103/PhysRevLett.127.172301 | DOI Listing |
J Hazard Mater
December 2024
College of Materials Science and Engineering, State Key Laboratory of Bio-Fiber and Eco-textiles, Collaborative Innovation Center for Marine Biobased Fibers and Ecological Textile Technology Institute of Marine Biobased Materials, Qingdao University, Qingdao 266071, China; College of Chemical Engineering and Technology, Yantai Nanshan University, Yantai 265713, China. Electronic address:
Selective autonomous enrichment of micropollutants in the aquatic media has attracted increasing attention because of their low concentration characteristics and diverse coexisting species. Herein, the gradient hydrogels were prepared via free redical polymerization of AA and NH-β-CD under the induction of unilateral UV illumination (P(AA-NH-β-CD)). The gradient hydrogels present autonomous enrichment towards Sb(III) with a higher selectivity both in single and binary solutions.
View Article and Find Full Text PDFInt J Biol Macromol
December 2024
MOE Engineering Research Center of Forestry Biomass Materials and Bioenergy, Beijing Forestry University, Beijing 100083, PR China. Electronic address:
Int J Biol Macromol
October 2024
College of Material Engineering, Fujian Agriculture and Forestry University, Fuzhou, Fujian 350108, PR China. Electronic address:
With the rapid advancement of flexible, portable devices, hydrogel electrolytes have gained considerable attention as potential replacements for conventional liquid electrolytes. A hydrogel electrolyte was synthesised by cross-linking acrylic acid (AA), acrylamide (AM), carboxymethyl cellulose (CMC), and zinc sulphate (ZnSO). The formation of hydrogen bonds and chelate interactions between the P(AA-co-AM) polymer, CMC, and ZnSO created a robust network, enhancing the mechanical properties of the hydrogel electrolytes.
View Article and Find Full Text PDFInt J Biol Macromol
June 2024
College of Environmental Science and Engineering, Beijing Forestry University, Beijing 100083, China. Electronic address:
In order to solve ecological remediation issues for abandoned mines with steep slopes, a kind of hydrogels with high cohesion and water-retaining were designed by inorganic mineral skeleton combining with polymeric organic network cavities. This eco-friendly hydrogel (MFA/HA-g-p(AA-co-AM)) was prepared with acrylic acid (AA)-acrylamide (AM) as network, which was grafted with humic acids (HA) as network binding point reinforcement skeleton and polar functional group donors, KOH-modified fly ash (MFA) as internal supporter. The maximum water absorption capacities were 1960 g/g for distilled water, which followed the pseudo-second-order model.
View Article and Find Full Text PDFACS Appl Mater Interfaces
January 2024
Key Lab of Colloid and Interface Chemistry, Shandong University, Jinan 250100, Shandong, P. R. China.
Supramolecular polymers offer promising potential for enhanced oil recovery (EOR) advancing techniques. Current instrumental analyses face limitations in capturing instantaneous intracomplex motions due to temporal and spatial constraints. The molecular mechanism of supramolecular polymer transport behavior within nanoconfinement is not yet fully understood.
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