NMR spectral study of two crystalline modifications of lithium metaborate,LiBO2

⁷Li and¹¹B NMR spectral parameters were obtained for the two structural modifications of lithium metaborate. We first studied the high-temperature -form of LiBO₂, _iso(¹¹ B) 0, e²qQ/h(¹¹B)=42.5±2.0 kHz, e²qQ/h(⁷Li)=155±5 kHz. The following values were obtained for monoclinic -LiBO₂ with tricoordination of the boron atom: _iso(¹¹ B) = 16±2, e²qQ/h(⁷Li)=32±10 kHz. The electric field gradient on the⁷Li and¹¹B nuclei in the different crystal positions was discussed.Institute of Silicate Chemistry, Academy of Sciences of the USSR. Translated from Zhurnal Strukturnoi Khimii, Vol. 30, No. 5, pp. 70–73, September–October, 1989.     

27Al and 23Na double-rotation NMR of sodalites.

The 27Al NMR spectra of calcium tungstate aluminate sodalite (CAW), Ca8[Al12O24](WO4)2, and the 23Na NMR spectra of sodium aluminosilicate sodalites of general composition Na9[Si6Al6O24]A2 with A = B(OH)4- (SBS), SCN- (SRS) and A2 = SO4(2-) (SSS), MoO4(2-) (SMS) have been measured using magic-angle spinning (MAS) and double-rotation (DOR) techniques. Rotor synchronized pulse excitation is applied in the DOR experiments. Dramatic line narrowing is observed in the DOR spectra of all samples. The 27Al DOR NMR spectra of CAW measured at 9.4 and 11.7 T and spinning rates of 800-1150 Hz of the outer and 5 kHz of the inner rotor show seven sharp central lines accompanied by a manifold of spinning sidebands. These lines correspond to the seven crystallographically inequivalent Al sites of the CAW framework derived from X-ray structure analysis. From the difference of the line positions in the 9.4 and 11.7 T spectra the quadrupole coupling constant, QCC, quadrupole induced shift, sigma qs, and isotropic chemical shift, delta cs, of each Al site have been calculated. QCC values in the range of 5 to 9 MHz are obtained which reflect the strong tetragonal distortion of the AlO4 tetrahedra in CAW. delta cs shows only small changes in the range between 74.4 and 77.2 ppm. A tentative assignment of all lines to the distinct Al sites is derived from the correlation between QCC and a "shear strain parameter" describing quantitatively the distortion of the AlO4 tetrahedra.(ABSTRACT TRUNCATED AT 250 WORDS)     

Effects of substrate and transfer on CVD-grown graphene over sapphire-induced Cu films

We differentiated the effects of Cu films deposited on single crystalline a-,r-,and c-plane sapphire substrates upon graphene films synthesized with atmospheric pressure chemical vapor deposition(CVD).The data illustrate that the realization of high-crystalline Cu film is dependent not only on the crystallinity of underlying substrate,but also on the symmetric match of crystallographic geometry between metal film and substrate.We also systematically investigated the effects of PMMA removal on the Raman ID/IG and IG/I2D values of transferred graphene.The results reveal that different PMMA removal methods do not alter the ID/IG values;instead,the residue of PMMA increases the IG/I2D values and the thermal decomposition of PMMA leads to higher IG/I2D values than the removal of PMMA with acetone.The effects of PMMA removal on variations of the Raman spectra are also discussed.     

Surface energy properties of lignin particles studied by inverse gas chromatography and interfacial adhesion in polyester composites with electromagnetic transparency

We introduce a simple spray drying method for the scaleup production of spherical organic (lignin) particles with sizes between 0.85 and 1.57 µm. We assess the surface energy of the lignin particles by inverse gas chromatography to reveal their role in composites synthesized with unsaturated polyester. Such nanocomposites are shown to be transparent to electromagnetic irradiation (millimeter wave bands). The permittivity and tanδ of the composite material reached values 3.01 and 0.01 at 28 GHz with 10% lignin content. Vinyl groups were introduced on the surface of the particles to achieve enhanced interfacial adhesion, and resulted in a reduced relative permittivity (2.75). Together with wave interactions, the mechanical and thermal properties of the composites are put in perspective, opening new opportunities in the development of bio-based devices for 5G high-speed communication.

     

Adsorptive Cathodic Stripping Voltammetry for Quantification of Alprazolam

A simple and highly sensitive electrochemical sensor was developed for adsorptive cathodic stripping voltammetry of alprazolam. Based on an electrochemically pretreated glassy carbon electrode, the sensor demonstrated good adsorption and electrochemical reduction of alprazolam. The morphology of the glassy carbon electrode and the electrochemically pretreated glassy carbon electrode were characterized by scanning electron microscopy/energy dispersive X-ray spectroscopy, Fourier transform infrared spectroscopy, cyclic voltammetry, and electrochemical impedance spectroscopy. The electrochemical behaviors of alprazolam were determined by cyclic voltammetry, and the analytical measurements were studied by adsorptive cathodic stripping voltammetry. Optimized operational conditions included the concentration and deposition time of sulfuric acid in the electrochemical pretreatment, preconcentration potential, and preconcentration time. Under optimal conditions, the developed alprazolam sensor displayed a quantification limit of 0.1 mg L⁻¹, a detection limit of 0.03 mg L⁻¹, a sensitivity of 67 µA mg⁻¹ L cm⁻² and two linear ranges: 0.1 to 4 and 4 to 20 mg L⁻¹. Sensor selectivity was excellent, and repeatability (%RSD < 4.24%) and recovery (82.0 ± 0.2 to 109.0 ± 0.3%) were good. The results of determining alprazolam in beverages with the developed system were in good agreement with results from the gas chromatography–mass spectrometric method.     

Comparison of the (17)O NMR spectra of zeolites LTA and LSX

¹⁷O NMR studies of various cation-exchanged LTA and LSX zeolites have shown similarities between the two systems. LSX samples containing divalent cations contain resonances with similar chemical shifts to those previously assigned to ‘bare’ framework oxygen atoms in Ca-LTA and Sr-LTA. The assignments are consistent with the trends seen in the spectra of monovalent cation-containing LSX and LTA zeolites, which show an increase in the average chemical shift with increasing cationic radius. The spectrum of Li-LSX, like Na-LSX, can be assigned based on the T–O–T bond angles. Gas sorption studies on Li-LSX are used to help identify the framework oxygen atoms that form the β-cages and demonstrate the sensitivity of the ¹⁷O shifts to gas loading.     

High-field high-speed MAS resolution enhancement in 1H NMR spectroscopy of solids

Resolution in ¹H NMR spectra of solids can be significantly enhanced with fast magic-angle spinning and high magnetic fields. A variable field and spinning speed study up to 25 T and 40 kHz shows that the homogeneous line broadening is inversely proportional to the product of magnetic field strength and spinning speed. The combination of high field and fast speed yields a ¹H linewidth approaching the intrinsic limit determined by anisotropy of magnetic susceptibility. An analysis of the anisotropic magnetic susceptibility line broadening is presented.     

Ramped-speed cross polarization MAS NMR

The inverse cubic dependency of the acceleration of a rotor on its diameter allows for mechanical dynamics comparable to spin dynamics in coupled spin systems. Rotor acceleration up to 300 kHz/s was measured. This feature can be used to simplify existing experiments and explore entirely new ones in the study of spin topologies and material properties.     

Two-dimensional triple-quantum Na MAS NMR spectroscopy of sodium cations in dehydrated zeolites

Two-dimensional triple-quantum (2D-3Q) ²³Na MAS NMR spectroscopy has been applied for the investigation of sodium cations in dehydrated zeolites NaY, NaEMT, NaZSM-5 and NaMOR. The experiments have shown that the new 2D-3Q technique allows the determination of the isotropic chemical shifts and quadrupolar couplings of sodium cations with SOQE (second-order quadrupolar effect) parameters of up to ca. 4 MHz. In the present work, SOQE parameters of 1.0–1.2 MHz were found for sodium cations located at positions SI in the hexagonal prisms of dehydrated zeolites NaY and NaEMT. The sodium cations located in the 10-ring and 12-ring channels of dehydrated zeolites NaZSM-5 and NaMOR, respectively, are characterized by a SOQE parameter of 2.0 MHz while a value of 3.1 MHz was determined for sodium cations in the sidepockets of the channels in dehydrated NaMOR.     

Simultaneous adiabatic spin-locking cross polarization in solid-state NMR of paramagnetic complexes

Continuous-wave irradiations cross polarization and its variations had not been a popular choice for sensitivity enhancement in paramagnetic solids due to the large spectral broadening and the effect of fast relaxation on both the source and target spins. Furthermore, with the application of very-fast sample spinning, which is the prerequisite for high-resolution purposes, polarization transfer over a large bandwidth is further degraded. In this work, we report a wideband sensitivity enhancement in paramagnetic solid with our recently developed technique, simultaneous adiabatic spin-locking cross polarization, SADIS CP. Experiments were demonstrated with Cu(II)(d,l-alanine)₂ · H₂O under high-static field of 14.1 T and very-fast sample spinning of 31 kHz.