Design techniques for voltage-to-time converters with nonlinearity emphasis

This paper provides an in-depth treatment of voltage-to-time converters (VTCs) for time-based signal processing with a nonlinearity emphasis. The need for VTCs in deployment of time-based techniques for high-speed or high-resolution analog-to-digital converters is investigated. It is followed with the classification of VTCs. A detailed treatment of the principle, topology, operation, and design consideration of variable-slope (VS) and constant-slope (CS) VTCs is provided. The nonlinearity of VS-VTCs and that of CS-VTCs are analyzed in detail analytically. It is shown that VS-VTCs is inherently nonlinear while CS-VTCs is intrinsically linear. Factors contributing to the nonlinearity of these VTCs are investigated. VS-VTCs and CS-VTCs studied are designed in TSMC 130 nm 1.2 V CMOS and analyzed using Spectre from Cadence Design Systems with BSIM3.3 device models. A good agreement between simulation and analytical results is obtained. The average gain of the VS-VTC is 4.4 times that of the CS-VTC. The 2nd and 3rd harmonics of the CS-VTC are significantly smaller as compared with those of the VS-VTC at the price of more power consumption.

     

Cryptanalysis of Two Signature Schemes for IoT and Mobile Health Systems

Wireless Personal Communications - Recently, Lee et al. (Sensors 20(14): 3983, 2020) proposed a certificateless aggregate arbitrated signature scheme CLAAS for IoT environments. Addobea et...     

Friendly spectrum jamming against MIMO eavesdropping

Wireless Networks - Friendly spectrum jamming is a flexible scheme to establish secure communications among heterogeneous wireless devices without the need of encryption. Previous works have...     

拟薄水铝石/陶瓷胶态加工浆料的流变性能

用拟薄水铝石纳米胶粒分散微米二硼化钛形成固含量为60Wt%的稳定陶瓷浆料,实验考察了拟薄水铝石固含量、二硼化钛固含量、温度对浆料流变性、稳定性的影响,对纳米γ-AlOOH胶粒分散微米TiB2的机制进行了讨论.大小约20nm的γ-AlOOH颗粒相互网联,成为外加微米陶瓷颗粒的骨架.浆料粘度随二硼化钛固含量的增加而增大,温度升高有利于胶体中薄水铝胶团与二硼化钛颗粒的相互作用并促进分散.     

Multinuclear NMR study of lanthanide(III) complexes of 1,2-PDTA in aqueous solution

The complexation of lanthanide(III) cations with 1,2-propanediaminetetraacetate (1,2-PDTA) in aqueous solution has been investigated by ¹⁰Na, ³⁵Cl, ²H and ¹¹O NMR shift measurements. It has been shown that the contact shifts are dominant for ¹⁷O, ¹⁶Cl and ²H (only for the heavier lanthanide series) and the pseudocontact shifts are dominant for ²⁵Na. It is suggested that the 1,2-PDTA ligand is bound pentadentately via the two nitrogens and the three carboxylates for the lighter lanthanide complexes, hexdentately via the two nitrogens and the four carboxylates for the heavier ones. The numbers of the water coordinated were determined. The small amount of chloride anion in inner coordination sphere was observed.     

Novel Phenomenon of Oxygen-to-oxygen Silyl Migration in Directed Aldol Reaction

The phenomenon of migration of the silyl groups from α-oxygen to β-oxygen in sodium aldol reaction was observed for the first time in this paper.     

Strategies for locating disulfide bonds in a monoclonal antibody via mass spectrometry

The location of the disulfide bonds in a recombinant monoclonal antibody was confirmed by matrix-assisted laser desorption/ionization-time-of-flight (MALDI-TOF) and electrospray ionization (ESI) mass spectrometry (MS). A non-reduced Endoproteinase Lys-C (Endo Lys-C) digest of the antibody was analyzed directly by MALDI-TOFMS. The sample was then reduced on-plate by depositing dithiothreitol (DTT) on the sample spot and re-analyzed by MALDI-TOFMS. The disulfide bonds were assigned based on the disappearance of certain mass ions in the non-reduced digest and the appearance of product ions in the reduced digest. A rapid LC/ESI-MS protocol was also developed to determine the location of the disulfide bonds. The peptides generated from the Endo Lys-C digest of the antibody were partially separated on a high performance liquid chromatography (HPLC) column by utilizing a steep gradient and analyzed by ESI-MS. The masses of the partially resolved peptides were determined by deconvoluting the mass spectra.     

The Tolman length: is it positive or negative?

By means of a large-scale molecular dynamics simulation, we show that the Tolman length, although positive, is much smaller in magnitude than previously reported. We found that the range of interparticle interaction can significantly affect the magnitude of the Tolman length. When the range of interaction is longer than five molecular diameters, the Tolman length is on the order of a few hundredths of the molecular diameter, rather than a few tenths known previously.