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91.
Let K be a compact convex subset of a separated locally convex space (over R) and let Ap(K) denote the space of all continuous real-valued affine mappings defined on K, endowed with the topology of pointwise convergence on the extreme points of K. In this paper we shall examine some topological properties of Ap(K). For example, we shall consider when Ap(K) is monolithic and when separable compact subsets of Ap(K) are metrizable. 相似文献
92.
Warren Wm. McGovern 《Journal of Pure and Applied Algebra》2008,212(2):340-348
Elementary divisor domains were defined by Kaplansky [I. Kaplansky, Elementary divisors and modules, Trans. Amer. Math. Soc. 66 (1949) 464-491] and generalized to rings with zero-divisors by Gillman and Henriksen [L. Gillman, M. Henriksen, Some remarks about elementary divisor rings, Trans. Amer. Math. Soc. 82 (1956) 362-365]. In [M.D. Larsen, W.J. Lewis, T.S. Shores, Elementary divisor rings and finitely presented modules, Trans. Amer. Math. Soc. 187 (1) (1974) 231-248], it was also proved that if a Hermite ring satisfies (N), then it is an elementary divisor ring. The aim of this article is to generalize this result (as well as others) to a much wider class of rings. Our main result is that Bézout rings whose proper homomorphic images all have stable range 1 (in particular, neat rings) are elementary divisor rings. 相似文献
93.
94.
95.
The reactions of the hydroxyl radical (at low pH) and SO4−. have been employed to oxidize a number of phenyl-substituted alcohols in aqueous solution; ESR spectroscopy has been employed
to study directly the radicals formed by fragmentation of first-formed radical-cations. Examples of deprotonation (to give
benzyl radicals), Cα−Cβ bond scission (e.g. PhCH2CH2OH to PhCH2
.) and longer-range fragmentation (e.g. PhCH2CH2CMe2OH to PhCH2CH2
.) are described and discussed: evidence is obtained for intramolecular nucleophilic attack as a route for overall electron-transfer
from side-chain to aromatic ring. Solvation of the proton and of oxygen-conjugated carbonium ions is thought, at least in
part, to account for differences between fragmentations induced in the gaseous and aqueous phases. 相似文献
96.
Amanda D. French Hannah M. Ashbaugh Gary Steinmetz Melanie Barnes Warren C. Conway David M. Klein 《International journal of environmental analytical chemistry》2017,97(6):499-507
The S.M.A.R.T. (small mass, affordable, rapid, transfer-less) digestion method was developed to determine heavy metal concentrations in small sample masses. The S.M.A.R.T. digestion method is a hot water bath digestion where sample digestion and dilution are performed in the original sample tube. This method is faster than the typical methods used and reduces potential sources of error. Masses as small as 0.01 g have been digested and analysed using this method. The preparation and digestion time is reduced from 10 h to less than 4 h. Acid volumes are reduced from millilitres to microlitres and the only disposable supplies needed are sample tubes and pipette tips. Method accuracy was determined by digesting seven replicates of two standard reference materials using the S.M.A.R.T. method and analysing samples by inductively coupled plasma mass spectrometry. The S.M.A.R.T. digestion method was found to provide excellent recoveries for Al (76 ± 2.7%), Mn (99 ± 11%), Co (92 ± 17%), Ni (93 ± 28%), Cu (109 ± 33%), Zn (97 ± 7.1%), As (108 ± 20%), Sr (90 ± 12%), Mo (84 ± 23%), Ag (91 ± 1.8%), Cd (95 ± 6.2%), Sn (139 ± 52%) and Pb (95 ± 22%). This study has successfully developed an efficient and reproducible digestion method for heavy metal determination in limited biomass samples. 相似文献
97.
Molecular dynamics simulations are used to investigate the effects of deformation on the segmental dynamics in an aging polymer glass. Individual particle trajectories are decomposed into a series of discontinuous hops, from which we obtain the full distribution of relaxation times and displacements under three deformation protocols: step stress (creep), step strain, and constant strain rate deformation. As in experiments, the dynamics can be accelerated by several orders of magnitude during deformation, and the history dependence is entirely erased during yield (mechanical rejuvenation). Aging can be explained as a result of the long tails in the relaxation time distribution of the glass, and similarly, mechanical rejuvenation is understood through the observed narrowing of this distribution during yield. Although the relaxation time distributions under deformation are highly protocol specific, in each case they may be described by a universal acceleration factor that depends only on the strain. 相似文献
98.
Necessary conditions for optimality in control problems with differential-inclusion dynamics have recently been developed
in the non-convex case by Clarke, Vinter, and others. Using appropriate reparametrizations of the time variable, we extend
these results to systems whose dynamics involve a differential inclusion where a vector-valued measure appears. An auxiliary
result central to our proof is an extension of existing free end-time necessary conditions to Clarke’s stratified framework. 相似文献
99.
Branca RT Jenista ER Warren WS 《Journal of magnetic resonance (San Diego, Calif. : 1997)》2011,209(2):347-351
Intermolecular dipolar interactions between proton and carbon spins can be used to indirectly detect carbon spectra with high sensitivity. In this communication, we present a modified sequence that, in addition to the high sensitivity of heteronuclear intermolecular multiple quantum coherence (iMQC) experiments, retains the line narrowing capability characteristic of homonuclear zero-quantum coherences. We demonstrate that this sequence can be used to obtain high resolution (13)C spectra in the presence of magnetic field inhomogeneities, both for thermal and hyperpolarized samples, and discuss applications to water-hyperpolarized carbon imaging. 相似文献
100.
Let m, m′, r, r′, t, t′ be positive integers with r, r′ ? 2. Let \(\mathbb{L}_r \) denote the ring that is universal with an invertible 1×r matrix. Let \(M_m (\mathbb{L}_r^{ \otimes t} )\) denote the ring of m × m matrices over the tensor product of t copies of \(\mathbb{L}_r \) . In a natural way, \(M_m (\mathbb{L}_r^{ \otimes t} )\) is a partially ordered ring with involution. Let \(PU_m (\mathbb{L}_r^{ \otimes t} )\) denote the group of positive unitary elements. We show that \(PU_m (\mathbb{L}_r^{ \otimes t} )\) is isomorphic to the Brin-Higman-Thompson group tV r,m ; the case t=1 was found by Pardo, that is, \(PU_m (\mathbb{L}_r )\) is isomorphic to the Higman-Thompson group V r,m . We survey arguments of Abrams, Ánh, Bleak, Brin, Higman, Lanoue, Pardo and Thompson that prove that t′V r′,m′ ≌ tV r,m if and only if r′ =r, t′ =t and gcd(m′, r′?1) = gcd(m, r?1) (if and only if \(M_{m'} (\mathbb{L}_{r'}^{ \otimes t'} )\) and \(M_m (\mathbb{L}_r^{ \otimes t} )\) are isomorphic as partially ordered rings with involution). 相似文献