A fractional order HIV-TB coinfection model with nonsingular Mittag-Leffler Law

The biological models for the study of human immunodeficiency virus (HIV) and its advanced stage acquired immune deficiency syndrome (AIDS) have been widely studied in last two decades. HIV virus can be transmitted by different means including blood, semen, preseminal fluid, rectal fluid, breast milk, and many more. Therefore, initiating HIV treatment with the TB treatment development has some advantages including less HIV-related losses and an inferior risk of HIV spread also having difficulties including incidence of immune reconstitution inflammatory syndrome (IRIS) because of a large pill encumbrance. It has been analyzed that patients with HIV have more weaker immune system and are susceptible to infections, for example, tuberculosis (TB). Keeping the importance of the HIV models, we are interested to consider an analysis of HIV-TB coinfected model in the Atangana-Baleanu fractional differential form. The model is studied for the existence, uniqueness of solution, Hyers-Ulam (HU) stability and numerical simulations with assumption of specific parameters.     

First observation of the P-wave spin-singlet bottomonium states hb(1P) and hb(2P)

We report the first observations of the spin-singlet bottomonium states h(b)(1P) and h(b)(2P). The states are produced in the reaction e(+)e(-)→h(b)(nP)π(+)π(-) using a 121.4 fb(-1) data sample collected at energies near the Υ(5S) resonance with the Belle detector at the KEKB asymmetric-energy e(+)e(-) collider. We determine M[h(b)(1P)]=(9898.2(-1.0-1.1)(+1.1+1.0)) MeV/c(2) and M[h(b)(2P)]=(10,259.8±0.6(-1.0)(+1.4)) MeV/c(2), which correspond to P-wave hyperfine splittings ΔM(HF)=(+1.7±1.5) and (+0.5(-1.2)(+1.6)) MeV/c(2), respectively. The significances of the h(b)(1P) and h(b)(2P) are 5.5σ and 11.2σ, respectively. We find that the production of the h(b)(1P) and h(b)(2P) is not suppressed relative to the production of the Υ(1S), Υ(2S), and Υ(3S).     

Growth of Fe-doped ZnO nanorods using aerosol-assisted chemical vapour deposition via in situ doping

In situ Fe doping of ZnO nanorods (NRs) was performed using aerosol assisted chemical vapour deposition (AA-CVD) technique. As the aerosol generator is located outside the reactor, AA-CVD provides the flexibility to control doping parameters, such as doping timing, doping duration and a wider choice of dopant precursors. The Fe dopant aerosol was flowed into the reactor during the growth of ZnO NRs to achieve in situ doping. The X-ray diffraction analysis indicates that the Fe dopants were introduced into the ZnO lattice and present mainly in the form of Fe²⁺. This result is supported by the X-ray photoelectron spectroscopy analysis as the doublet separation is 13.6 eV, although there is a shift of Fe_1/2 and Fe_3/2 peaks to a lower binding energy levels. A strong green emission of PL of Fe-doped ZnO NRs shows that the NRs have poor crystal quality attributed to the Fe-induced defects (recombination centres). The poor photocatalytic performance in degrading Rhodamine B solution of Fe-doped ZnO NRs further proves that the Fe-induced defects were recombination centres rather than traps. Lastly, the growth mechanism of in situ Fe doping of ZnO NRs was discussed.     

Comparison of amine-induced cyclization of 6-chloro-1-hexynylphosphonate and isobutyl 7-chlorohept-2-ynoate

The reaction of 6-chloro-1-hexynylphosphonate with primary and secondary amines afforded exclusively 2-aminocyclohexenylphosphonates in 62-85% isolated yields. In contrast, reaction of various amines with isobutyl 7-chlorohept-2-ynoate in acetonitrile at 70 °C gave (E)-sec-butyl 2-(1-alkylpiperidin-2-ylidene)acetates in 65-78% isolated yields. Calculations offer an explanation for the difference in the behavior of the two compounds classes. It is shown that C-C cyclization in the alkyne-phosphonate group occurs via an initial formation of a zwitterionic intermediate, which is stabilized by both an inductive effect of the phosphonate group and a newly formed hydrogen bond. The alkyne-carboxylate group, on the other hand, proceeds via enamine formation as a result of the smaller inductive effect of the carboxylate combined with involvement of an allene-like resonance form. This resonance form both delocalizes the negative charge in the zwitterionic intermediate making it to be less available for attack, and affects the geometry thus preventing formation of the stabilizing hydrogen bond. Hence, the zwitterionic intermediate of the alkyne-carboxylates is less stable leading to formation of an enamine, which is followed by N-C cyclization to give the azaheterocycles.     

Preparation of 5-hydroxy-1-alkenyboronates from 1-alkynylboronates, Cp2ZrCl2/2EtMgBr, and aldehydes

1-Alkynylboronates form five-membered zirconacycles with Cp(2)ZrCl(2)/2-EtMgBr as indicated by deuterium labeling. The zirconacycles add aldehydes to form seven-membered zirconacycles. Hydrolysis of the latter provides 5-hydroxy-1-alkenylboronates in fair to good isolated yields. Both aliphatic and aromatic aldehydes undergo insertion.     

Direct contact versus solvent-shared ion pairs in NiCl2 electrolytes monitored by multiplet effects at Ni(II) L edge X-ray absorption

We investigate the local electronic structure in aqueous NiCl2 electrolytes by Ni L edge X-ray absorption spectroscopy. The experimental findings are interpreted in conjunction with multiplet calculations of the electronic structure and the resulting spectral shape. In contrast to the situation in the solid, the electronic structure in the electrolyte reflects the absence of direct contact Ni-Cl ion pairs. We observe a systematic change of the intensity ratio of singlet- and triplet-related spectral features as a function of electrolyte concentration. These changes can be described theoretically by a change in the weight of transition matrix contributions with different symmetries. We interpret these findings as being due to progressive distortions of the local symmetry induced by solvent-shared ion pairs.     

Polymers-Copolymer as Flow Improvers for Fuel Oils and Their Electrical Conductivity

In order to find efficient cold flow improvers for fuel oil, polymethylmethacrylate (PMMA), polystyrene (PS), and a copolymer [styrene (S)–methylmethacrylate (MMA) were prepared. The structure of these polymers and the copolymer were characterized by infrared spectral analysis and their molecular weights were measured. These polymers-copolymer were used as additives for fuel oils in order to lower their pour point. Accordingly, they were evaluated as flow improvers for fuel oil. The results indicated that PMMA possesses less performance as pour point depressant. While the addition of PS and the copolymer (S–MMA) yield excellent pour point depressants for fuel oil. Upon studying the prepared additives and their properties, it was found that the electrical properties of the copolymer were changed due to the presence of polar ion in MMA effect on the electrical properties. The highest electrical conductivity was found when styrene:MMA molar ratio was 1:1.     

Effects of polyvinylpyrrolidone on structural and optical properties of willemite semiconductor nanoparticles by polymer thermal treatment method

Journal of Thermal Analysis and Calorimetry - Willemite is an inorganic semiconductor material used for optoelectronic applications. The present study purposes a new polymer thermal treatment...