Probabilistic evaluation of interconnectable capacity for wind power generation

We propose a novel framework for probabilistic evaluation of interconnectable capacity for wind power generation. This is based on mathematical modeling of load frequency control systems, which captures their nonlinear (saturation and rate limiting) dynamical characteristics, and stochastic uncertainty of wind power output deviation. The method called stochastic linearization is used to analyze resulting power quality. The effectiveness of the proposed method is examined by numerical simulation.     

Tetrachloroferrate (III) Salts of BDH-TTP [2,5-Bis(1,3-dithiolan-2-ylidene)-1,3,4,6-tetrathiapentalene] and BDA-TTP [2,5-Bis(1,3-dithian-2-ylidene)-1,3,4,6-tetrathiapentalene]: Crystal Structures and Physical Properties

Three FeCl₄ salts based on non-tetrathiafulvalene (TTF) donors, 2,5-bis(1,3-dithiolan-2-ylidene)-1,3,4,6-tetrathiapentalene (BDH-TTP) and 2,5-bis(1,3-dithian-2-ylidene)-1,3,4,6-tetrathiapentalene (BDA-TTP), have been prepared and characterized as κ-(BDH-TTP)₂FeCl₄, β-(BDA-TTP)₂FeCl₄, and (BDA-TTP)₃FeCl₄ · PhCl. The κ-(BDH-TTP)₂FeCl₄ salt, with a room-temperature conductivity (σ_rt) of 39 S cm⁻¹, is metallic down to 1.5 K, and its magnetic susceptibility obeys the Curie-Weiss law with a Curie constant (C) of 4.25 emu K mol⁻¹ and a Weiss constant (θ) of 0.041 K. β-(BDA-TTP)₂FeCl₄ exhibits metallic behavior (σ_rt=9.4 S cm⁻¹) with a sharp metal-to-insulator (MI) transition (T_MI=113 K) and antiferromagnetic ordering with the Néel temperature of near 8.5 K, whereas the solvated (BDA-TTP)₃FeCl₄ · PhCl salt is a semiconductor with a thermal activation energy of 0.11 eV (σ_rt=2.0× 10⁻² S cm⁻¹) and exhibits Curie-Weiss behavior (C=4.42 emu K mol⁻¹, θ=−0.35 K).     

Direct monitoring of DNA cleavages catalyzed by an ATP-dependent deoxyribonuclease on a 27 MHz quartz-crystal microbalance

Kinetic studies of enzymatic DNA cleavage reactions (the enzyme binding, hydrolysis along DNA strands, and then release of the enzyme from the completely hydrolyzed ssDNA) were carried out on a 27 MHz quartz-crystal microbalance.     

Temperature dependence of the dynamic interstitial interactions in potassium bromide

Formation of the H and H_A centers in Na⁺-doped KBr within the time constant of the thermal annihilation of the H center is measured between 80 and 200K and it is shown that the volume of the interaction of the radiation-induced replacement sequence of an interstitial halogen with a Na⁺ impurity increases with an activation energy of (0.025 ± 0.005) eV as the temperature rises.     

Colloid chemical studies of polystyrene latices polymerized without any surface-active agents

Summary The influence of secondary minimum for the stability of spherical colloid has been studied using a series of soap-free polystyrene latices from 350 m to 1400 m in diameter.The critical flocculation concentration (c. f. c.) and the zeta-potential at the c. f. c. for each latex were determined with several salts of different ionic valencies. The values of c. f. c. varied with the particle size, reaching a maximum value at 750 m and then decreasing gradually with the diameter.Another phenomenon detected in the experiment was the complete reversibility of coagulation which was observed only in the cases of large size latices, i. e., the coagulates of large size particles were fully redispersed in the solution by stirring. The time-dependence of their sedimentation curves was reproducible.These experimental results could not be explained by the simple theoretical consideration for stability of suspension. The satisfactory explanation is given only using the term of secondary minimum of interaction potential, i. e., the origin of coagulation was shifted from the ordinary primary minimum to the shallow secondary minimum at about 750 m of the particle diameter.

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Zusammenfassung Der Einfluß des Sekundär-Minimum auf die Stabilität von Kolloiden wurde an seifenfreien Polystyrol-Latex-Suspensionen mit einem Durchmesser von 350 m bis 1400 m untersucht. Die kritische Flockungskonzentration (c. f. c.) und das Zeta-Potential bei c. f. c. wurde mit verschiedenen Salzen bestimmt.Der Wert von c. f. c. ändert sich mit der Teilchengröße.Ein weiterer wichtiger experimenteller Befund ist die vollständige Reversibilität der Flockung bei größeren Latices.Derartige Versuchsergebnisse können durch das Sekundär-Minimum befriedigend erklärt werden.

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With 7 figures in 10 details and 2 tables     

Intramolecular participation in alkoxycarbenium ion pools

[reaction: see text] Alkoxycarbenium ions having no substituents on the cationic carbon have been accumulated as "cation pools" by the introduction of an ether group in an appropriate position. Intramolecular participation of the ether oxygen is suggested to be responsible for stabilization of the alkoxycarbenium ions.     

High-fidelity teleportation beyond the no-cloning limit and entanglement swapping for continuous variables

We experimentally demonstrate continuous-variable quantum teleportation beyond the no-cloning limit. We teleport a coherent state and achieve the fidelity of 0.70 +/- 0.02 that surpasses the no-cloning limit of 2/3. Surpassing the limit is necessary to transfer the nonclassicality of an input quantum state. By using our high-fidelity teleporter, we demonstrate entanglement swapping, namely, teleportation of quantum entanglement, as an example of transfer of nonclassicality.     

Novel efficient routes to heparin monosaccharides and disaccharides achieved via regio- and stereoselective glycosidation

A new methodology for the synthesis of heparin building blocks has been developed. We describe novel efficient routes to both L-iduronic acid and D-glucuronic acid acceptors. Glycosylation with thioglycosides donors gave corresponding disaccharides in a regio- and stereoselective fashion. An improved approach to synthesizing azido-glucose thioglycoside donor to render azido-sugar from mannose via nucleophilic substitution is described. [reaction: see text]     

Frequency dependence of acoustic properties of aqueous glucose solutions in the VHF/UHF range

The bioultrasonic spectroscopy system was employed for measurements of velocity and attenuation coefficient of glucose solutions in the VHF/UHF range. The relation between the slope of the square of velocity and the relaxation parameters, and the relation between the frequency exponent on attenuation coefficient and the relaxation parameters are investigated. In order to carry out numerical calculations, a model for a single relaxation process is employed, wherein the attenuation coefficient is expressed as (A/( 1 + (f/falpha)2) + B)f2 where falpha is the attenuation relaxation frequency, and A and B are constants. The numerical calculations show that the slope of the square of the velocity is determined uniquely by the velocity relaxation frequency fv and v(infinity)2 - v(0)2 where v0 is the zero-frequency velocity and v(infinity) is the infinite-frequency velocity, and that the frequency exponent on the attenuation coefficient is determined uniquely by falpha and A/B. For experimental considerations, the velocities and the attenuation coefficients of 5, 15, and 25% concentration aqueous solutions of glucose were measured in the frequency range 20 to 700 MHz. The data for the 5 and 15% aqueous solutions can be explained using the single relaxation model. However, the data for the 25% aqueous solution suggest the existence of multirelaxation processes.