Development and use of reference materials in India – status and plans

Reference materials development activities in India started during the period 1955–1960 for quality control in the production and use of drugs and pharmaceuticals. While the practice of import and distribution gradually accelerated in some areas, including medical, environment etc., the earliest known development of Certified Reference Materials (CRMs) within the country began with the preparation of metallurgical CRMs somewhere around 1965. A few more area-specific programs involving preparation of CRMs for quality control in the electronic industries, food and food products etc., began in the past decade. A common national program covering these activities was initiated in 1996, through organization of a national workshop on the subject and formation of a National Task Force for the development and use of reference materials in the country. The existing status and the priority needs of reference materials have been compiled by the Task Force, and a program has also been prepared for development of some of the urgently required CRMs within the country.

     

Statistical and Criticality Analysis of the Lower Ionosphere Prior to the 30 October 2020 Samos (Greece) Earthquake (M6.9), Based on VLF Electromagnetic Propagation Data as Recorded by a New VLF/LF Receiver Installed in Athens (Greece)

In this work we present the statistical and criticality analysis of the very low frequency (VLF) sub-ionospheric propagation data recorded by a VLF/LF radio receiver which has recently been established at the University of West Attica in Athens (Greece). We investigate a very recent, strong (M6.9), and shallow earthquake (EQ) that occurred on 30 October 2020, very close to the northern coast of the island of Samos (Greece). We focus on the reception data from two VLF transmitters, located in Turkey and Israel, on the basis that the EQ’s epicenter was located within or very close to the 5th Fresnel zone, respectively, of the corresponding sub-ionospheric propagation path. Firstly, we employed in our study the conventional analyses known as the nighttime fluctuation method (NFM) and the terminator time method (TTM), aiming to reveal any statistical anomalies prior to the EQ’s occurrence. These analyses revealed statistical anomalies in the studied sub-ionospheric propagation paths within ~2 weeks and a few days before the EQ’s occurrence. Secondly, we performed criticality analysis using two well-established complex systems’ time series analysis methods—the natural time (NT) analysis method, and the method of critical fluctuations (MCF). The NT analysis method was applied to the VLF propagation quantities of the NFM, revealing criticality indications over a period of ~2 weeks prior to the Samos EQ, whereas MCF was applied to the raw receiver amplitude data, uncovering the time excerpts of the analyzed time series that present criticality which were closest before the Samos EQ. Interestingly, power-law indications were also found shortly after the EQ’s occurrence. However, it is shown that these do not correspond to criticality related to EQ preparation processes. Finally, it is noted that no other complex space-sourced or geophysical phenomenon that could disturb the lower ionosphere did occur during the studied time period or close after, corroborating the view that our results prior to the Samos EQ are likely related to this mainshock.     

Stability study and time resolution measurement of straw tube detectors

Pramana - This article provides numerical simulations of the time-fractional coupled Korteweg–de Vries and Klein–Gordon equations via the local meshless collocation method (LMCM)...     

The Efficiency of the Metal Catalysts in the Nucleophilic Substitution of Alcohols is Dependent on the Nucleophile and Not on the Electrophile

In this study, we investigate the effect of the electrophiles and the nucleophiles for eight catalysts in the catalytic S_N1 type substitution of alcohols with different degree of activation by sulfur‐, carbon‐, oxygen‐, and nitrogen‐centered nucleophiles. The catalysts do not show any general variance in efficiency or selectivity with respect to the alcohols and follow the trend of alcohol reactivity. However, when it comes to the nucleophile, the eight catalysts show general and specific variances in the efficiency and selectivity to perform the desired substitution. Interestingly, the selectivity of the alcohols to produce the desired substitution products was found to be independent of the electrophilicity of the generated carbocations but highly dependent on the ease of formation of the cation. Catalysts based on iron(III), bismuth(III), and gold(III) show higher conversions for S‐, C‐, and N‐centered nucleophiles, and Bi^III was the most efficient catalyst in all combinations. Catalysts based on rhenium(I) or rhenium(VII), palladium(II), and lanthanum(III) were the most efficient in performing the nucleophilic substitution on the various alcohols with the O‐centered nucleophiles. These catalysts generate the symmetrical ether as a by‐product from the reactions of S‐, C‐, and N‐centered nucleophiles as well, resulting in lower chemoselectivity.     

Dioxygen activation in photooxidation of diphenylmethane by a dioxomolybdenum(VI) complex anchored covalently onto mesoporous titania

A dioxomolybdenum(VI) complex has been covalently anchored onto mesoporous titania by a silicon-assisted transesterification route. The grafting of the complex to the mesoporous structure was confirmed by diffuse reflectance infrared Fourier transform, Raman and UV–Vis spectroscopy and by nitrogen sorption experiments. The ability of the grafted complex to activate molecular oxygen (O₂) has been evaluated in the photooxidation of diphenylmethane to produce benzophenone. The photooxidation of diphenylmethane was monitored continuously by in situ dispersive Raman spectroscopy. A scheme for the activation of molecular oxygen under very mild conditions is proposed. A comparison with the same complex anchored onto commercial titanium P-25 and silica gel revealed both the beneficial effect of the mesoporous structure and the existence of a synergistic effect between MoO/TiO₂/O₂/light entities, which promotes the photooxidation process under green chemistry conditions. Finally, the heterogeneous catalyst is sustainable; it can be recycled and reused without significant loss in activity or selectivity.     

Highly Converged Valence Bands and Ultralow Lattice Thermal Conductivity for High‐Performance SnTe Thermoelectrics

A two‐step optimization strategy is used to improve the thermoelectric performance of SnTe via modulating the electronic structure and phonon transport. The electrical transport of self‐compensated SnTe (that is, Sn_1.03Te) was first optimized by Ag doping, which resulted in an optimized carrier concentration. Subsequently, Mn doping in Sn_1.03?xAg_xTe resulted in highly converged valence bands, which improved the Seebeck coefficient. The energy gap between the light and heavy hole bands, i.e. ΔE_v decreases to 0.10 eV in Sn_0.83Ag_0.03Mn_0.17Te compared to the value of 0.35 eV in pristine SnTe. As a result, a high power factor of ca. 24.8 μW cm^?1 K^?2 at 816 K in Sn_0.83Ag_0.03Mn_0.17Te was attained. The lattice thermal conductivity of Sn_0.83Ag_0.03Mn_0.17Te reached to an ultralow value (ca. 0.3 W m^?1 K^?1) at 865 K, owing to the formation of Ag₇Te₄ nanoprecipitates in SnTe matrix. A high thermoelectric figure of merit (z T≈1.45 at 865 K) was obtained in Sn_0.83Ag_0.03Mn_0.17Te.     

Octanuclear Ni4Ln4 Coordination Aggregates from Schiff Base Anion Supports and Connecting of Two Ni2Ln2 Cubes: Syntheses,Structures, and Magnetic Properties

A family of 3d–4f aggregates have been reported through guiding the dual coordination modes of ligand anion (HL^?) and in situ generated ancillary bridge driven self‐assembly coordination responses toward two different types of metal ions. Reactions of lanthanide(III) nitrate (Ln=Gd, Tb, Dy, Ho and Yb), nickel(II) acetate and phenol‐based ditopic ligand anion of 2‐[{(2‐hydroxypropyl)imino}methyl]‐6‐methoxyphenol (H₂L) in MeCN‐MeOH (3 : 1) mixture and LiOH provided five new octanuclear Ni‐4f coordination aggregates from two Ni₂Ln₂ cubanes. Single‐crystal X‐ray diffraction analysis reveals that all the members of the family are isostructural, with the central core formed from the coupling of two distorted [Ni₂Ln₂O₄] heterometallic cubanes [Ni₂Ln₂(HL)₂(μ₃‐OH)₂(OH)(OAc)₄]⁺ (Ln=Gd ( 1 ), Tb ( 2 ), Dy ( 3 ), Ho ( 4 ) and Yb ( 5 )). Higher coordination demand of 4f ions induced the coupling of the two cubes by (OH)(OAc)₂ bridges. Variable temperature magnetic study reveals weak coupling between the Ni²⁺ and Ln³⁺ ions. For the Tb ( 2 ) and Dy ( 3 ) analogs, the compounds are SMMs without an applied dc field, whereas the Gd ( 1 ) analogue is not an SMM. The observation revealed thus that the anisotropy of the Ln³⁺ ions is central to display the SMM behavior within this structurally intriguing family of compounds.     

Interaction of α-Synuclein with Phospholipids and the Associated Restructuring of Interfacial Lipid Water: An Interface-Selective Vibrational Spectroscopic Study

Interaction of α-Synuclein (αS) with biological lipids is crucial for the onset of its fibrillation at the cell membrane/water interface. Probed herein is the interaction of αS with membrane-mimicking lipid monolayer/water interfaces. The results depict that αS interacts negligibly with zwitterionic lipids, but strongly affects the pristine air/water and charged lipid/water interfaces by perturbing the structure and orientation of the interfacial water. The net negative αS (−9 in bulk water; pH 7.4) reorients the water as hydrogen-up (H-up) at the air/water interface, and electrostatically interacts with positively charged lipids, making the interface nearly net neutral. αS also interacts with negatively charged lipids: the net H-up orientation of the interfacial water decreases at the anionic lipid/water interface, revealing a domain-specific interaction of net negative αS with the negatively charged lipids at the membrane surface.