Effect of Radio-Frequency and Low-Frequency Bias Voltage on the Formation of Amorphous Carbon Films Deposited by Plasma Enhanced Chemical Vapor Deposition

The effect of radio-frequency （RF） or low-frequency （LF） bias voltage on the for- mation of amorphous hydrogenated carbon （a-C：H） films was studied on silicon substrates with a low methane （CH4） concentration （2-10 vol.%） in CH4＋Ar mixtures. The bias substrate was applied either by RF （13.56 MHz） or by LF （150 kHz） power supply. The highest hardness values （~18-22 GPa） with lower hydrogen content in the fihns （~20 at.%） deposited at 10 vol.% CH4, was achieved by using the RF bias, However, the films deposited using the LF bias, under similar RF plasma generation power and CH4 concentration （50 W and 10 vol.%, respectively）, displayed lower hardness （~6-12 GPa） with high hydrogen content （~40 at.%）. The structures analyzed by Fourier Transform Infrared （FTIR） and Raman scattering measurements provide an indication of trans-polyacetylene structure formation. However, its excessive formation in the films deposited by the LF bias method is consistent with its higher bonded hydrogen concentration and low level of hardness, as compared to the film prepared by the RF bias method. It was found that the effect of RF bias on the film structure and properties is stronger than the effect of the low-frequency （LF） bias under identical radio-frequency （RF） powered electrode and identical PECVD （plasma enhanced chemical vapor deposition） system configuration.     

The combined influence of Mg and Ca on microstructural evolution of alumina

The solubility limits of Ca and Mg co-doped in alumina at 1600°C were determined by equilibrating alumina saturated with Ca and Mg. This resulted in the formation of MgAl₂O₄ (Mg spinel), CaO·6Al₂O₃ (CA6), Ca₂Mg₂Al₂₈O₄₆ (CAM-II), and alumina grains saturated with Mg and Ca. Under these conditions, the amount of Ca and Mg in the alumina grains represents the solubility limits. The solubility limits were measured using a fully standardized wavelength dispersive spectrometer mounted on a scanning electron microscope. In the co-doped state, the solubility limit of Ca in alumina was 32 ± 13 ppm, and the solubility limit of Mg in alumina was 210 ± 43 ppm. The presence of Ca results in an increase of the solubility limit of Mg in alumina from 132 to 210 ppm, suggesting that the increased Mg in solution results in more Mg excess at the alumina grain boundaries, thus contributing to a decreased grain-boundary mobility by solute-drag.     

1H‐decoupling and Isotopic Labeling for the Measurement of the Longitudinal Relaxation Time of Hyperpolarized 13C‐Methylenes in Choline Analogs

The T₁ of a hyperpolarized site in solution is a key parameter that determines the time‐window in which its NMR signals are observable. For ¹³C sites adjacent to protons, ¹H‐decoupling has been shown to increase the hyperpolarized signal resolution and SNR. Additionally, polarization transfer to protons has shown utility in increasing the sensitivity of detection. However, ¹H‐decoupling could lead to a change in the decay rate of a hyperpolarized ¹³C site. Here we tested this possible effect in a case where the protons are directly bound to an sp³ hyperpolarized ¹³C site (using [1,2‐¹³C₂]choline) and ¹H‐decoupling was applied continuously throughout the hyperpolarized decay measurement. We found that ¹H‐decoupling did not lead to any significant changes in the ¹³C polarization decay time but did result in the expected collapse of J‐coupling and produced sharper signals. This result suggested that ¹H‐decoupling did not affect the decay rate of hyperpolarized sp^{3 13}C sites. The deuterium‐substitution approach (using [1,1,2,2‐D₄,1‐¹³C]choline) showed a dramatic prolongation of T₁. Upper bounds on the T₁ of all investigated sites were calculated.     

Magnetic Assembly of a Multifunctional Guidance Conduit for Peripheral Nerve Repair

Nerve growth conduits are designed to support and promote axon regeneration following nerve injuries. Multifunctionalized conduits with combined physical and chemical cues, are a promising avenue aimed at overcoming current therapeutic barriers. However, the efficacious assembly of conduits that promote neuronal growth remains a challenge. Here, a biomimetic regenerative gel is developed, that integrates physical and chemical cues in a biocompatible “one pot reaction” strategy. The collagen gel is enriched with magnetic nanoparticles coated with nerve growth factor (NGF). Then, through a remote magnetic actuation, highly aligned fibrillar gel structure embedded with anisotropically distributed coated nanoparticles, combining multiple regenerating strategies, is obtained. The effects of the multifunctional gels are examined in vitro, and in vivo in a 10-mm rat sciatic nerve injury model. The magneto-based therapeutic conduits demonstrate oriented and directed axonal growth, and improve nerve regeneration in vivo. The study of multifunctional guidance scaffolds that can be implemented efficiently and remotely provides the foundation to a novel therapeutic approach to overcome current medical obstacles for nerve injuries.     

Working beyond the static limits of laser stability by use of adaptive and polarization-conjugation optics

Strong thermo-optical aberrations in flash-lamp-pumped Nd:Cr:GSGG rods were corrected to yield TEM(00) output at twice the efficiency of Nd:YAG. A hemispherical resonator operating at the limit of stability was employed. As much as 3 W of average power in a Gaussian beam (M(2) approximately 1) was generated. Unique features were zero warm-up time and the ability to vary the repetition rate without varying energy, near- and far-field profiles, or polarization purity. Thermal focusing and astigmatism were corrected with a microprocessor-controlled adaptive-optics backmirror composed of discrete elements (variable-radius mirror). A reentrant resonator coupled polarizer losses back into the laser rod and corrected depolarization.     

A survey on low-power wide area networks for IoT applications

Telecommunication Systems - We are on the entry of the exponential advancement of the internet-of-things (IoT) due to the quick development of internet-connected smart-objects. As the number of...     

Potent inhibitors of the human UDP-glucuronosyltransferase 2B7 derived from the sesquiterpenoid alcohol longifolol

The tricyclic sesquiterpenol (+)-longifolol served as a lead structure for the design of inhibitors of the human UDP-glucuronosyltransferase (UGT) 2B7. Twenty-four homochiral and epimeric longifolol derivatives were synthesized and screened for their ability to inhibit the enzyme. The absolute configuration at the stereogenic center C1' was determined by X-ray crystallography and 2D NMR spectroscopy (gHSQC, gNOESY). The phenyl-substituted secondary alcohol 16 b (beta-phenyllongifolol) displayed the highest affinity toward UGT2B7, and its inhibitory dissociation constant was 0.91 nM. The mode of inhibition was rapidly reversible and competitive. The inhibitor was not glucuronidated by UGT2B7 or other hepatic UGTs, presumably as a result of the high steric demand exerted by the phenyl group. Inhibition assays employing 14 other UGT isoforms suggested that inhibitor 16 b was highly selective for UGT2B7.     

Stereochemical and steric control of the UDP-glucuronosyltransferase-catalyzed conjugation reaction: a rational approach for the design of inhibitors for the human UGT2B7

A set of 76 derivatives of the epimeric tricyclic sesquiterpenols longifolol and isolongifolol was subjected to inhibition and glucuronidation assays employing the human UDP-glucuronosyltransferase (UGT) 2B7. Detailed structure-activity relationships (SARs) with respect to functionality, stereochemical properties, and steric features were derived. To gain further insight into the SARs of UGT2B7 ligands herein, we have developed a 3D-quantitative structure-activity relationship (3D-QSAR) using Comparative Molecular Similarity Analysis (CoMSIA). The formation of the enzyme-inhibitor complex was predominantly controlled by spatially directed hydrophobic interactions. The glucuronidation rate was significantly influenced by the steric demand of substituents in proximity of the nucleophilic hydroxy group. The glucuronidation of the compounds was prevented by the introduction of bulky substituents such as isopropyl, tert-butyl, and phenyl groups. The epimeric longifolol derivatives of series D were the best inhibitors displaying IC(50) values as low as 4.6 nM. This study shows that high-potency substrates can be turned into potent inhibitors by addressing functional, stereochemical, and steric properties.     

Experimental validation of an optimization formulation of the human grasping quality sense

An experimental procedure that evaluates the quality of a grasp is developed. In this procedure human subjects grasp a rigid object that is subjected to an external load. Three formulations that capture the sense of grasping quality through the energy level stored in the gripper, maximum value of the applied finger forces, and through the distribution of the grasping forces are considered. The applied finger forces are measured and the quality values of the grasp based on these three different formulations are computed. These grasping quality values are compared with numerical human assessments, that are obtained via a psychophysical magnitude estimation method. We derive an augmented weighted functional that combines these three formulations, and show that it exhibits a high correlation with human quality assessment. Our results demonstrate that the most dominant mechanism that characterizes the quality of a rigid body grasp is the uniformity level of the contact forces. © 1997 John Wiley & Sons, Inc.     

Development of organosilicone–polyurethanes as stone preservation and consolidation materials

Two organosilicone-modified polyurethanes are investigated as potential materials for the conservation and consolidation of natural stones. The materials are low molecular weight oligomers at the application stage and react with the humidity of the air to give polymers, forming continuous microlayers. The two differ in the length of the organosilicone chain, resulting in pronounced differences in their physical state: one forms a brittle glassy material (T_g ≈ 70°C). and the other, a soft rubbery material (T_g ≈ −100°C). The rate of the polymerization of the prepolymers was investigated at different conditions, showing a strong dependence on the presence of a catalyst and air humidity. Both these favorable conditions exist probably in the natural stone pores, enhancing the formation of the protective hydrophobic internal microlayer. © 1996 John Wiley & Sons, Inc.