Constraining the position of the knee in the galactic cosmic ray spectrum with ultra-high-energy diffuse γ\gamma-rays

The diffuse $\gamma$-ray emission was measured up to $957$ TeV by the Tibet-AS$\gamma$ experiment recently. Assuming that it is produced by the hadronic interaction between cosmic ray nuclei and the interstellar medium, it requires that the cosmic ray nuclei should be accelerated well beyond PeV energies. Measurements of the cosmic ray spectra for different species show diverse results at present. The Tibet experiments showed that the spectrum of proton plus helium has an early knee below PeV. If this is correct, the diffuse $\gamma$-ray emission would suggest an additional component of Galactic cosmic rays above PeV energies. This second component may originate from a source population of so-called PeVatrons revealed by recent ultra-high energy $\gamma$-ray observations, and could contribute to the cosmic ray fluxes up to the energy of the second knee. On the other hand, the KASCADE measurement showed that the knee of protons is higher than PeV. In this case, the diffuse $\gamma$-rays observed by Tibet-AS$\gamma$ can be well accounted for by only one cosmic ray component. These two scenarious (ie. the Tibet and KASCADE knees) could be distinguished by the spectral structures of diffuse $\gamma$-rays and cosmic ray nuclei. Future measurements of spectra of individual nuclei by HERD and LHAASO experiments and diffuse $\gamma$-rays by LHAASO can jointly constrain these two scenarios.Comment: 9 pages,4 figures. accepted by Ap

Identify the topological superconducting order in a multi-band quantum wire

How to distinguish the zero-bias peak (ZBP) caused by the Majorana fermions from that by the other effects remains a challenge in detecting the topological order of a quantum wire. In this paper we propose to distinguish the topological superconducting phase from the topologically trivial phase by making a Josephson junction of the quantum wire attached to a side lead and then measuring the tunneling conductance through it as the phase difference across the junction $\phi$ varies. Even if the ZBPs exist in both phases, we can identify the topological superconducting phase by a conductance peak at $\phi=\pi$ and a nearby butterfly pattern.Comment: 5 pages, 4 figure

Zelena sinteza i primjena zeolita ZSM-5

A ZSM-5 molecular sieve composite with a wide pore prepared by the solid phase in-situ synthesis method and fluid catalytic cracking, and an FCC catalyst additive prepared by the same ZSM-5 molecular sieve for increasing the amount of light olefin yield were investigated. The samples were characterized by XRD, N2 adsorption/desorption, SEM, and NH3-TPD, respectively. The results showed that the structure of the ZSM-5 molecular sieve composite prepared by solid phase in-situ synthesis method was pure MFI-type zeolite material. The crystallinity of ZSM-5 molecular sieve was 59.8 wt%. The synthesized ZSM-5 molecular sieve had more acid content and a wide-pore structure. The average pore size was 5.9 nm, and BET specific surface area and micropore specific surface area of sample were 213 m2 g–1 and 124 m2 g–1, respectively. The evaluated results indicated that the FCC catalyst additive had good selectivity for LPG, propylene, and butene, increasing propylene and butene yields by 2.28 wt% and 2.15 wt%, respectively, as well as had better heavy oil cracking capability and coke selectivity. This work is licensed under a Creative Commons Attribution 4.0 International License.Istražen je kompozit molekularnog sita ZSM-5 sa širokim porama pripremljen sintezom na krutoj fazi in-situ i katalitičkim krekiranjem u vrtložnom sloju (FCC) te aditiv katalizatora FCC pripremljen istim molekularnim sitom ZSM-5 u svrhu povećanja količine prinosa lakog olefina. Uzorci su karakterizirani rendgenskom difrakcijom na prahu (XRD), adsorpcijom/desorpcijom N2, skenirajućim elektronskim mikroskopom (SEM) te temperaturno programiranom desorpcijom amonijaka (NH3-TPD). Rezultati su pokazali da je struktura smjese molekularnog sita ZSM-5 pripremljena metodom sinteze in-situ u čvrstoj fazi čisti zeolitni materijal skupine MFI. Kristaliničnost molekularnog sita ZSM-5 iznosila je 59,8 %. Sintetizirano molekularno sito ZSM-5 imalo je više kiseline i strukturu sa širokim porama. Prosječna veličina pora bila je 5,9 nm, a specifična površina (BET) i specifična površina mikropora uzoraka iznosile su 213 m2 g–1, odnosno 124 m2 g–1. Evaluirani rezultati ukazali su na to da aditiv katalizatora FCC pokazuje dobru selektivnost za ukapljeni naftni plin (UNP), propilen i buten, povećavajući prinos propilena i butena za 2,28 %, odnosno 2,15 %, kao i da ima bolju sposobnost krekiranja teškog ulja i selektivnost koksa. Ovo djelo je dano na korištenje pod licencom Creative Commons Imenovanje 4.0 međunarodna

Identification of Fur in Pasteurella multocida and the Potential of Its Mutant as an Attenuated Live Vaccine

Pasteurella multocida is a pathogenic microorganism that causes a variety of serious diseases in humans and animals worldwide. The global regulator gene, fur, plays an important role in pathogenesis and regulates the virulence of many bacteria. Here, we identified a fur gene in P. multocida by complementing a Salmonella Choleraesuis Δfur mutant, and characterized a fur mutant strain of P. multocida. The P. multocida Δfur mutant strain exhibited no significant differences in growth and outer membrane protein (OMP) profiles when the complemented strain was compared to the parent. Ducks were used as the model organism to determine the virulence and protection efficacy induced by Δfur mutant strain. Animal experiments showed that colonization by the mutant was decreased by oral infection of live Δfur mutant strain. The LD50 of the ducks infected with the Δfur mutant was 146-fold higher than that of the ducks infected with the wild-type strain when administered through the oral route. Evaluation of the immunogenicity and protective efficacy of the Δfur mutant of P. multocida revealed strong serum IgY and bile IgA immune responses following oral inoculation with the Δfur strain. Ducks that were orally inoculated with the Δfur mutant strain demonstrated 62% protection efficacy against severe lethal challenge with the wild-type P. multocida. This study provides new insights into P. multocida virulence and the potential use of an attenuated vaccine against P. multocida

3-Nitro-2-phenyl­chroman

In the title compound, C15H13NO3, the dihedral angle between the two aromatic rings is 79.25 (16)°

Experimental and theoretical analysis of microstructural evolution and deformation behaviors of CuW composites during equal channel angular pressing

CuW composites were synthesized using an equal channel angular pressing (ECAP) technique. Microstructural evolution during sintering process was investigated using both optical microscopy and transmission electron microscopy (TEM), and their deformation mechanisms were studied using finite element analysis (FEA). Results showed severe plastic deformation of the CuW composites and effective refinement of W grains after the ECAP process. TEM observation revealed that the ECAP process resulted in lamellar bands with high densities dislocations inside the composites. Effects of extrusion temperature and extrusion angles on stress-strain relationship and sizes of deformation zones after the ECAP process were investigated both theoretically and experimentally. When the extrusion angle was 90°, a maximum equivalent stress of ~1001 MPa was obtained when the extrusion test was done at room temperature of 22 °C, and this value was lower than compression strength of the CuW composites (1105.43 MPa). The maximum equivalent strains were varied between 0.5 and 0.7. However, when the extrusion temperature was increased to 550 °C and further to 900 °C, the maximum equivalent stresses were decreased sharply, with readings of 311 MPa and 68 MPa, respectively. When the extrusion angle was increased to 135°, the maximum equivalent stresses were found to be 716.9 MPa, 208 MPa, and 32 MPa for the samples extruded at temperatures of 22 °C, 550 °C and 900 °C, respectively. Simultaneously, the maximum equivalent strains were decreased to 0.2–0.4. Furthermore, results showed that the maximum equivalent stress was located on the sample's external surface and the stress values were gradually decreased from the surface to the center of samples, and the magnitudes of plastic deformation zones at the surface were much larger than those at the central part of the sintered samples. FEA simulation results were in good agreements with experimentally measured ones

Adsorpcija Cu2+, Zn2+ i Ni2+ iona na adsorbens pripremljen iz potrošenog FCC katalizatora i kremenih diatomita

An adsorbent prepared from fluid catalytic cracking (FCC) spent catalyst fines and diatomite, and its adsorption of Cu2+, Zn2+, and Ni2+ ions were investigated. The adsorbent was characterized by XRD, SEM, and N2 adsorption-desorption techniques. The results showed that the specific surface area and pore volume of adsorbent increased with the increase in FCC spent catalyst fines. The influence factors on the adsorption of the adsorbents were studied. The suitable adsorption conditions were: pH value of 5.0, ratio of solid to liquid of 1 : 600 (g:ml), adsorption time of 4 h, room temperature. The adsorption of metal ions varied with the type of metal cations. The adsorption isotherms suggested that the sequence of the adsorption efficiency was Cu2+ > Zn2+ > Ni2+. The amount of Cu2+, Zn2+, and Ni2+ metal ion adsorbed onto the adsorbent was 49.17 mg g–1, 46.83 mg g–1, and 35.72 mg g–1, respectively. The adsorption data of Cu2+, Zn2+, and Ni2+ ions fitted well with the Freundlich adsorption isotherm model. This work is licensed under a Creative Commons Attribution 4.0 International License.Ispitivan je adsorbens pripremljen iz katalizatora za katalitičko krekiranje u vrtložnom sloju (FCC) i diatomita, te njegova adsorpcija iona Cu2+, Zn2+ i Ni2+. Adsorbens je karakteriziran XRD, SEM i N2 adsorpcijsko-desorpcijskim tehnikama. Rezultati su pokazali da se specifična površina i volumen pora adsorbensa povećavaju s povećanjem količine potrošenog katalizatora FCC. Proučavani su čimbenici utjecaja na adsorpciju adsorbensa. Prikladni uvjeti adsorpcije bili su: pH vrijednost 5,0, omjer čvrste tvari i kapljevine 1 : 600 (g:ml), vrijeme adsorpcije 4 h i sobna temperatura. Adsorpcija metalnih iona varira s tipom metalnih kationa. Adsorpcijske izoterme pokazale su da je slijed učinkovitosti adsorpcije Cu2+ > Zn2+ > Ni2+. Količina metalnih iona Cu2+, Zn2+ i Ni2+ adsorbiranih na adsorbensu iznosila je 49,17 mg g–1, 46,83 mg g–1, odnosno 35,72 mg g–1. Podatci o adsorpciji iona Cu2+, Zn2+ i Ni2+ slijede model Freundlichove adsorpcijske izoterme. Ovo djelo je dano na korištenje pod licencom Creative Commons Imenovanje 4.0 međunarodna