Results from Super-Kamiokande and K2K

Results from Super-Kamiokande-I’s entire 1496 live days of solar neutrino data are presented, including the absolute flux, energy spectrum, zenith angle (day/night) and seasonal variation. The possibility of MSW and vacuum oscillations is discussed in light of these results. Results from the first 1289 days of Super-K-I’s atmospheric neutrino analysis are also presented, including the evidence for ν_μ →ν _τ oscillations, against ν_μ → ν_sterile oscillations, and the current limits on proton decay. Finally, results based on 56 × 10¹⁹ protons on target are given for the K2K long-baseline neutrino oscillation experiment.     

Thermal degradation and flame retardance in copolymers of methyl methacrylate with diethyl(methacryloyloxymethyl)phosphonate

Methyl methacrylate (MMA) has been free radically copolymerized, both in bulk and in solution, with diethyl(methacryloyloxymethyl)phosphonate (DEMMP), to give polymers which are significantly flame retarded when compared with PMMA, as indicated by the results of limiting oxygen index (LOI) measurements, UL 94 tests, and the results of cone calorimetric experiments. The physical and mechanical properties of the copolymers are similar to those of PMMA, except that the bulk copolymers are slightly crosslinked, and are better than those of PMMA flame retarded to a similar extent by some phosphate and phosphonate additives. Examination of the some of the gaseous products of pyrolysis and combustion, and of chars produced on burning, show that flame retardation occurs in the copolymers by both a condensed-phase and a vapour-phase mechanism. The condensed-phase mechanism is shown to involve generation of phosphorus acid species followed by reaction of these with MMA units giving rise to methacrylic acid units. The methacrylic acid units subsequently form anhydride links, which probably impede depolymerization of the remaining MMA sequences, resulting in evolution of less MMA (the major fuel when MMA-based polymers burn). By undergoing decarboxylation, leading to interchain cyclisation and, eventually, to aromaticisation, the anhydride units are probably also the principal precursors to char.     

Classification and discrete cocompact subgroups of some 7-dimensional connected nilpotent groups

Summary For real connected nilpotent groups, 7 is the lowest dimension where there are infinitely many non-isomorphic groups, and also where some groups (indeed, uncountably many) have no discrete cocompact subgroups. In [21] one infinite family <InlineEquation ID=IE"1"><EquationSource Format="TEX"><![CDATA[<InlineEquation ID=IE"2"><EquationSource Format="TEX"><![CDATA[<InlineEquation ID=IE"3"><EquationSource Format="TEX"><![CDATA[<InlineEquation ID=IE"4"><EquationSource Format="TEX"><![CDATA[<InlineEquation ID=IE"5"><EquationSource Format="TEX"><![CDATA[<InlineEquation ID=IE"6"><EquationSource Format="TEX"><![CDATA[<InlineEquation ID=IE"7"><EquationSource Format="TEX"><![CDATA[<InlineEquation ID=IE"8"><EquationSource Format="TEX"><![CDATA[$]]></EquationSource></InlineEquation>]]></EquationSource></InlineEquation>]]></EquationSource></InlineEquation>]]></EquationSource></InlineEquation>]]></EquationSource></InlineEquation>]]></EquationSource></InlineEquation>]]></EquationSource></InlineEquation>]]></EquationSource></InlineEquation>\mathcal{G}$ of 7-dimensional groups was identified and classified. Discrete cocompact subgroups H were identified for some groups in $\mathcal{G}$ in [10], along with simple quotients of $C^{*}(\mathrm{H})$ and relevant flows $(\mathrm{H}_3,\mathbf{T}^3)$. In this paper, such H and attributes are determined for more groups in $\mathcal{G}$; in particular, the members of $\mathcal{G}$ that admit discrete cocompact subgroups are identified precisely. In achieving some of these results, we consider other known ways of classifying the groups in $\mathcal{G}$, and also the classification of the analogous family of complex groups.     

Non-invasive measurement of void fraction and liquid temperature in microchannel flow boiling

Past thermometry research for two-phase microfluidic systems made much progress regarding wall temperature distributions, yet the direct measurement of fluid temperature has received little attention. This paper uses a non-invasive two-dye/two-color fluorescent technique to capture fluid temperature along with local liquid fraction in a two-phase microflow generated by injecting air into a heated microchannel. The fluorescent emission of Rhodamine 110 and Rhodamine B, measured with photodiodes, is used to obtain local liquid temperature (±3°C) and void fraction (±2% full-scale) over a temperature range from 45 to 100°C. Arrays of these sensors can significantly expand the set of measurable flow parameters to include bubble/slug frequency, size, velocity, and growth rates in addition to mapping the local liquid temperature and void fraction.     

C*-Algebras Characterized by Ergodic Actions of the n-Torus

Using basic harmonic analysis on the n-torus, it is shown thatthe non-commutative n-tori are the only primitive C*-algebras(up to isomorphism) on which the n-torus Tⁿ acts freely andergodically. An explicit construction recovers the generatingunitaries in a natural way from the action. 2000 MathematicsSubject Classification 46L55.     

Cyclopropyl alkynes as mechanistic probes to distinguish between vinyl radical and ionic intermediates

[reaction: see text] The reactions of (trans-2-phenylcyclopropyl)ethyne, 1a, (trans,trans-2-methoxy-3-phenylcyclopropyl)ethyne, 1b, and (trans,trans-2-methoxy-1-methyl-3-phenylcyclopropyl)ethyne, 1c, with either aqueous sulfuric acid or tris(trimethylsilyl)silane (or tributyltin hydride) and AIBN have been investigated. Protonation and addition of the silyl (or stannyl) radical occurred at the terminal position of the alkyne giving an alpha-cyclopropyl-substituted vinyl cation or radical, respectively. Under both reaction conditions, 1a yielded products derived from ring opening toward the phenyl substituent. Alkynes 1b and 1c, however, gave different products depending on whether radical or cationic conditions were used. When radical conditions were employed, products derived from regioselective ring opening toward the phenyl substituent were obtained. In contrast, when cationic conditions were employed, products derived from selective ring opening toward the methoxy substituent were isolated. The corresponding alpha-cyclopropyl-substituted vinyllithium derivatives were also synthesized and were found to be stable toward rearrangement. An estimate of the rate constants for ring opening of the alpha-cyclopropylvinyl cations was also made: values of 10(10)-10(12) s(-1) were found for the vinyl cations derived from protonation of the terminal carbon of alkynes 1a-c. Based on these results, cyclopropyl alkynes 1a-c can be classified as hypersensitive mechanistic probes for the detection of vinyl radical or cationic intermediates generated adjacent to the cyclopropyl ring and, in the case of 1b and 1c, the distinction between a radical or cationic intermediate is possible.     

On the Structure of Minimal Left Ideals in the Largest Compactification of a Locally Compact Group

This paper is centred around a single question: can a minimalleft ideal L in G^LUC, the largest semi-group compactificationof a locally compact group G, be itself algebraically a group?Our answer is no (unless G is compact). In deriving this conclusion,we obtain for nearly all groups the stronger result that nomaximal subgroup in L can be closed. A feature of our work isthat completely different techniques are required for the connectedand totally disconnected cases. For the former, we can relyon the extensive structure theory of connected, non-compact,locally compact groups to derive the solution from the commutativecase, using some reduction lemmas. The latter directly involvestopological dynamics; we construct a compact space and an actionof G on it which has pathological properties. We obtain otherresults as tools towards our main goal or as consequences ofour methods. Thus we find an extension to earlier work on therelationship between minimal left ideals in G^LUC and H^LUC whenH is a closed subgroup of G with G/H compact. We show that thedistal compactification of G is finite if and only if the almostperiodic compactification of G is finite. Finally, we use ourmethods to show that there is no finite subset of G^LUC invariantunder the right action of G when G is an almost connected groupor an IN-group.     

Analysis on discrete cocompact subgroups of the generic filiform Lie groups

Summary Let F_n, n≧ 1, denote the sequence of generic filiform (connected, simply connected) Lie groups. Here we study, for each F_n, the infinite dimensional simple quotients of the group C*-algebra of (the most obvious) one of its discrete cocompact subgroups D_n. For D_n, the most attractive concrete faithful representations are given in terms of Anzai flows, in analogy with the representations of the discrete Heisenberg group H₃ ⊆G₃ on L²(T) that result from the irrational rotation flows on T; the representations of D_n generate infinite-dimensional simple quotients A_n,θ of the group C*-algebra C*(D_n). For n>1, there are other infinite-dimensional simple quotients of C*(D_n) arising from non-faithful representations of D_n. Flows for these are determined, and they are also characterized and represented as matrix algebras over simple affine Furstenberg transformation group C*-algebras of the lower dimensional tori.