The acoustic signature of bubbles fragmenting in sheared flow

Measurements of the sound of bubbles fragmenting in fluid shear are presented and analyzed. The frequency, amplitude, and decay rate of the acoustic emissions from 1.8-mm-radius bubbles fragmenting between opposed fluid jets have been determined. A broad band of frequencies (1.8 to 30 kHz) is observed with peak pressure amplitudes in the range of 0.03 to 2 Pa. While the peak pressure amplitudes show no significant scaling with frequency, the frequency dependence of the decay rates is consistent with the sum of thermal and acoustic radiation losses.     

In Situ Quenching Methods Toward exo-Olefin-Terminated Polyisobutylene

exo-Olefin-terminated polyisobutylene was obtained directly from living isobutylene polymerizations by addition of a quenching compound to the living chain ends. Three broad classes of compounds were evaluated including hindered bases such as hindered pyridines and piperidines, N-hydro-2,5-disubstitutedpyrroles, and sulfides, ethers, and silylethers. The proposed mechanism of quenching unique to each class was discussed, with supporting kinetic, spectroscopic, and structure-based evidence presented. Hindered bases were proposed to operate by E2 elimination reaction of free base at the carbenium ion. N-Hydro-2,5-disubstitutedpyrroles were proposed to form the η⁵-2,5-disubstitutedpyrrolyltrichloro-titanium(IV) coordination complex, which serves as the true quencher. Sulfides, ethers, and silylethers were proposed to operate by first converting the PIB chain ends quantitatively to the onium adduct, which is then decomposed to form exo-olefin PIB. Sulfides and ethers were the best performing quenchers of all the types studied, particularly bulky ones such di-tert-butylsulfide and diisopropyl ether.     

Apparent anomalous fading of thermoluminescence associated with competition with radiationless transitions

Anomalous fading of thermoluminescence (TL) is the effect of a fading which is significantly faster than what is warranted by the trapping parameters which are evaluated from the features of the TL peak in question. A previous work suggested that in certain cases, apparent anomalous fading may be a normal fading in disguise. The idea was that, at least in some cases, radiationless transitions into competing recombination centers may yield a very narrow peak which, while using either the curve fit technique or the different peak shape method will result in very high values of effective activation energy E and frequency factor s which, in turn, will yield an apparent life-time orders of magnitude higher than the real one. The question has been raised whether this anomaly is observable only when the peak shape methods are utilized and in particular, can the same effect occur when the broadly used initial-rise method is applied. It is demonstrated in this work that under similar circumstances of competition, very high effective values of E and s are evaluated which result in very high life-times when the activation energy is evaluated by the initial-rise method. Thus, the explanation of apparent anomalous fading as being a normal decay in disguise, is extended to cases in which the initial-rise method is utilized for the parameter evaluation.     

On base radical and semisimple classes defined by class operators

By using class operators, we define base radical and semisimple classes, within a broad abstract setting due to Puczylowski. The new notions agree with the usual Kurosh–Amitsur ones for associative rings and groups but differ for not necessarily associative rings, in general lying strictly between the Kurosh–Amitsur and torsion theory notions. A study of the class operators for their own sake is initiated, and a connection with modal logic is made.     

A biosynthetically-inspired synthesis of the tetrahydrofuran core of obtusallenes II and IV

[reaction: see text] Sharpless asymmetric dihydroxylation was regioselective for the trans olefin in an E vs Z vs terminal triene substrate. To test a biosynthetic hypothesis, the resulting diol underwent diastereoselective bromoetherification to provide the des-chloro core of marine natural products obtusallenes II and IV. Alternatively, anionic chloride ring-opening of a Z-beta,gamma-unsaturated epoxide gave separable regioisomeric halohydrins. Bromoetherification gave the fully elaborated core of obtusallenes II and IV with all of the relative stereochemistry correctly set.     

Extending the time range of luminescence dating using red TL (RTL) from volcanic quartz

The potential of red thermoluminescence (RTL) emission from quartz, as a dosimeter for baked sediments and volcanic deposits, has received some attention over the past decade. While there have been some important observations relating to signal stability, saturation characteristics and emission wavebands, there has not been a systematic analysis of RTL properties of older (i.e., >1 Ma), quartz-bearing known age volcanic deposits. We have undertaken such an analysis using independently-dated silicic volcanic deposits from New Zealand, ranging in age from 300 ka through to 1.6 Ma. We observed a complex RTL emission in most volcanic quartzes, which consists of a number of discrete high temperature (i.e, >220°C) TL peaks. Isothermal analysis indicates a stable dating trap (E=2.03 eV; S=4.20×10¹⁵) which is stable at ambient (c. 20°C) temperatures for >10⁹ a. We confirm the slow onset of saturation with dose, and the limited extent of sensitivity changes due to dosing and TL readout. As such, there is much potential for exploiting the dosimeter in dating studies and we present the results from a modified single aliquot regenerative (SAR) procedures which indicate that there is a good agreement between RTL dating and other methods over time scales 10⁵–10⁶ a. This paper presents a summary of the most important related results of our findings and outlines the configuration of photomultiplier and filter combinations which maximizes RTL detection for temperatures up to 500°C.     

Synthesis of anti and syn hydroxy-iso-evoninic acids

The first synthesis of hydroxy-iso-evoninic acid (2), a pyridyl diacid found as a macrodilactone bridging ligand in bioactive Celastraceae sesquiterpenoid-based natural products, has been achieved in 9 steps and an overall yield of 26%. The synthesis utilizes a benzilic ester rearrangement (BER) and a late stage benzylic oxidation to give access to all four stereoisomers whose absolute stereochemistry was assigned following chromatographic separation and anomalous dispersion X-ray crystallography.     

Density,conductance, transference numbers,and diffusion measurements in concentrated solutions of nickel chloride at 25°C

The Hittorf technique for measuring transference numbers has been modified to produce precise data in concentrated aqueous electrolyte solutions. Density, molar conductance, transference number, tracer-diffusion, and mutual diffusion data are reported for aqueous NiCl₂ solutions up to 4M concentration at 25°C.Visiting Fellow at the Australian National University on leave from the School of Chemical Sciences, Universiti Sains Malaysia, Penang, Malaysia.     

Sets with B-action and linear algebra

Let B be a Boolean ring. Any unital B-module M has a B-action given by for all . We show that any set with B-action may be represented as a subset with B-action of a unital B-module. We extend this to algebras with B-action and apply it to if-then-else algebras over Boolean algebras by viewing them as semilattices with B-action. Received May 23, 1996; accepted in final form February 4, 1998.