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1.
Atomic-scale friction of a tungsten tip on a graphite surface   总被引:1,自引:0,他引:1  
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2.
We construct two bases of the natural numbers B1 and B2, eachof order two, such that (B1 + B2 (n) <n+c/(log n). For alower estimate, it is proved that if B2 and are two bases, eachof order two, then (B1+B2)(n) > n. Generalisations to sumsof bases of order h > 2 are also given.  相似文献   
3.
Data are presented which show that when a polymer contains an appreciable amount of low molecular weight species below the diffusion limit of the osmometer membrane, the osmotic molecular weight, M?n, is generally higher than the M?n calculated from gel-permeation chromatography (GPC). Experiments were performed on samples of poly(vinyl chloride) (PVC) and high-cis polybutadiene polymers. Osmotic data were obtained in the usual manner, while GPC data were obtained using the universal calibration approach. It was found that when all polymer species below approximately 10,000 molecular weight were excluded from the calculation of M?n by GPC, agreement in M?n was obtained between membrane osmometry and GPC. The data obtained suggest that the choice of M?n as measured by membrane osmometry in the calibration of the GPC should not be done casually, as the measured M?n may not reflect the “true” value of that sample, especially when the polymer sample contains an appreciable amount of low molecular weight material.  相似文献   
4.
The pointwise ergodic theorem is proved for prime powers for functions inL p,p>1. This extends a result of Bourgain where he proved a similar theorem forp>(1+√3)/2. This paper is a part of the author’s Ph.D. thesis supervised by V. Bergelson.  相似文献   
5.
In this Note, we present a new formalism for nonlinear and non-separable multiscale representations. The new formalism we propose brings about similarities between existing nonlinear multiscale representations and also allows us to alleviate the classical hypotheses made to prove the convergence of the multiscale representations.  相似文献   
6.

1,4-Dichlorobenzene is a frequently used lavatory deodorant although it has strong endocrine disrupting and potential carcinogenic effects. A large amount (approximately 15,000 tonnes annually worldwide) of this compound is released into the environment. This paper deals with the determination of 1,4-dichlorobenzene in a variety of environmental matrices. Various extraction and concentration methods such as charcoal absorbtion tubes and headspace sampling were applied. Sensitive and selective ion monitoring GC-MS measurements were used for determination. Significant concentrations of the compound have been identified in lavatory air, waste water, waste water sludge and human breast milk.

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Recent methods developed by Tao [18], Kolountzakis and Matolcsi [7] have led to counterexamples to Fugelde’s Spectral Set Conjecture in both directions. Namely, in Tao produced a spectral set which is not a tile, while Kolountzakis and Matolcsi showed an example of a nonspectral tile. In search of lower dimensional nonspectral tiles we were led to investigate the Universal Spectrum Conjecture (USC) of Lagarias and Wang [14]. In particular, we prove here that the USC and the "tile → spectral" direction of Fuglede’s conjecture are equivalent in any dimensions. Also, we show by an example that the sufficient condition of Lagarias and Szabó [13] for the existence of universal spectra is not necessary. This fact causes considerable difficulties in producing lower dimensional examples of tiles which have no spectra. We overcome these difficulties by invoking some ideas of Révész and Farkas [2], and obtain nonspectral tiles in . Fuglede’s conjecture and the Universal Spectrum Conjecture remains open in 1 and 2 dimensions. The one-dimensional case is closely related to a number theoretical conjecture on tilings by Coven and Meyerowitz [1].  相似文献   
9.
Journal of Nonlinear Science - The isothermal quasistatic (i.e. acceleration neglected) hardening-free plasticity at large strains is considered, based on the standard multiplicative decomposition...  相似文献   
10.
Three novel tricyclic diamines (1,7-diazaisoadamantane, 1,5-diazaisoadamantane and 1,6-diazahomobrendane) were prepared. A flexible synthetic strategy was employed which used flat, aromatic azaindoles as the starting materials. The requisite azaindoles were prepared by a tandem Sonogashira coupling/intramolecular cyclization reaction. Ring saturation, appropriate functionalization and intramolecular alkylation provided the three novel tricyclic diamines cores.  相似文献   
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