High Temperature Phase Stability in Li0.12Na0.88NbO3: A Combined powder X-Ray and Neutron Diffraction Study

Lithium doped sodium niobate is an ecofriendly piezoelectric material that exhibits a variety of structural phase transitions with composition and temperature. We have investigated the phase stabilities of an important composition Li0.12Na0.88NbO3 (LNN12) using a combination of powder x-ray and neutron diffraction techniques in the temperature range 300 - 1100 K. Detailed Rietveld analyses of thermo-diffractograms show a variety of structural phase transitions ranging from non-polar antiferrodistortive to ferroelectric in nature. In the temperature range of 525 K to 675 K, unambiguous experimental evidence is shown for phase coexistence of orthorhombic paraelectric O1 phase (space group Cmcm) and orthorhombic ferroelectric O2 phase (space group Pmc21). The bp primitive lattice parameter of the ferroelectric orthorhombic phase (O2 phase) decreases, while the ap and cp primitive lattice parameters show normal increase with increase in temperature. Above 675 K, in the O1 phase, all lattice parameters come close to each other and increase continuously with increase of temperature, and around 925 K, ap parameter approaches bp parameter and thus the sample undergoes an orthorhombic to tetragonal phase transition. Further as temperature increases, the cp lattice parameter decreases, and finally approaches to ap parameter, and the sample transform into the cubic phase. The continuous change in the lattice parameters reveals that the successive phase transformations from orthorhombic O1 to high temperature tetragonal phase and finally to the cubic phase are not of a strong first order type in nature. We argue that application of chemical pressure as a result of Li substitution in NaNbO3 matrix, favours the freezing of zone centre phonons over the zone boundary phonons that are known to freeze in pure NaNbO3 as function of temperature.Comment: 15 pages, 5 Figures. arXiv admin note: text overlap with arXiv:1011.441

Preparation and in vitro evaluation of primaquine-conjugated gum arabic microspheres

Gum arabic, a branched polysaccharide, was oxidized using periodate to generate reactive aldehyde groups on the biopolymer. Primaquine, an 8-aminoquinoline, was covalently coupled onto oxidized gum arabic via an imine bond and simultaneously fabricated into microspheres of less than 2 μm in size by heat denaturation in a reverse emulsion of 1:1 light paraffin oil and toluene stabilized by sorbitan sesquioleate as the surfactant. The covalent binding of primaquine to the polysaccharide using the clinically used water-soluble form of the drug primaquine phosphate was achieved in the presence of borate buffer of pH 11. Up to 35% of the drug could be bound to the polymer backbone depending on the concentration of the drug employed initially and the degree of oxidation of the polysaccharide. Interestingly, both the aliphatic and the hindered aromatic amino groups of primaquine were found to react with the aldehyde functions through Schiff base formation leading to cross-linking of the polysaccharide with the drug itself. In vitro release of the drug from microspheres into phosphate buffered saline (PBS, pH 7.4, 0.1 M) at 37 °C showed that the release of primaquine from the matrix was slow, although gradually increased with time. The maximum released was below 50% of the drug payload even after 10 days. Release into simulated gastric and intestinal fluids was faster compared to the release in PBS due to rapid hydrolysis of the Schiff's linkage in the gastric fluid. A possible reason for the poor hydrolytic susceptibility of the Schiff's linkage is suggested based on the unequal reactivity of the amino groups on primaquine and its relevance in possible therapeutic application of this polymer-drug conjugate discussed

Performance measures for upper gastrointestinal endoscopy:A European Society of Gastrointestinal Endoscopy (ESGE) Quality Improvement Initiative

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Persistent Pneumothorax: Alveolar pleural fistula due to a hole in a bulla

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A case report of long-latency evoked diaphragm potentials after exposure to acute intermittent hypoxia in post-West Nile virus meningoencephalitis

We present a case report of a 42-year-old female with post-West Nile virus meningoencephalitis who exhibited unique, long-latency diaphragm potentials evoked by transcranial and cervical magnetic stimulation after exposure to acute intermittent hypoxia (AIH). The subject was recruited for a study investigating AIH effects on respiratory motor function in healthy individuals. She had contracted West Nile virus infection 5 years before assessment that resulted in hospitalization and persistent allodynia but was not reported to the research team. During the study, transcranial (TMS) and cervical (CMS) magnetic stimulation were performed before and 30-60 min after a single presentation of AIH [15, 1-min hypoxic episodes (∼9% inspired O2), with 1-min normoxic intervals]. Diaphragm EMG was recorded using chest wall surface electrodes. At baseline, evoked diaphragm potentials were within normal ranges for both TMS (onset latency = 17.0 ± 1.1 ms; peak-to-peak amplitude = 220 ± 27 µV) and CMS (onset latency = 7.8 ± 0.6 ms; peak-to-peak amplitude = 336 ± 8 µV). However, long-latency TMS- and CMS-evoked potentials were observed 30-60 min post-AIH that were not present at baseline nor in healthy subjects. The onset of long-latency potentials ranged from 50 to 808 ms. While AIH is a potentially useful therapeutic strategy to enhance motor function after neurological disease or injury, it may elicit distinct effects in individuals with a history of neuroinfectious disease. Possible explanations for these unusual responses are discussed

Are lead-free relaxor ferroelectric materials the most promising candidates for energy storage capacitors?

Dielectric capacitors offer high-power density and ultrafast discharging times as compared to electrochemical capacitors and batteries, making them potential candidates for pulsed power technologies (PPT). However, low energy density in different dielectric materials such as linear dielectrics (LDs), ferroelectrics (FEs), and anti-ferroelectric (AFEs) owing to their low polarization, large hysteresis loss and low breakdown strength, respectively, limits their real time applications. Thus, achieving a material with high dielectric constant, large dielectric breakdown strength and slim hysteresis is imperative to obtain superior energy performance. In this context, relaxor ferroelectrics (RFEs) emerged as the most promising solution for energy storage capacitors. This review starts with a brief introduction of different energy storage devices and current advances of dielectric capacitors in PPT. The latest developments on lead-free RFEs including bismuth alkali titanate based, barium titanate based, alkaline niobite based perovskites both in ceramics and thin films are comprehensively discussed. Further, we highlight the different strategies used to enhance their energy storage performance to meet the requirements of the energy storage world. We also provide future guidelines in this field and therefore, this article opens a window for the current advancement in the energy storage properties of RFEs in a systematic way.This study has been partially supported by (i) DST-SERB, Govt. of India through Grant ECR/2017/000068 (KCS), (ii) UGC through grant nos. F.4-5(59-FRP)/ 2014(BSR) and (iii) Portuguese Foundation for Science and Technology (FCT) in the framework of the Strategic Funding UIDB/FIS/04650/2020 (JPBS). The author A. R. Jayakrishnan acknowledges the Central University of Tamil Nadu, India for his Ph. D fellowship. The authors acknowledge the CERIC-ERIC Consortium for access to experimental facilities and financial support under proposal 20192055