Multiple recurrence and nilsequences

Aiming at a simultaneous extension of Khintchine(X,X,m,T)(X,\mathcal{X},\mu,T) and a set A ? XA\in\mathcal{X} of positive measure, the set of integers n such that A T^2nA T^knA)(A)^k+1-\mu(A{\cap} T^{n}A{\cap} T^{2n}A{\cap} \ldots{\cap} T^{kn}A)>\mu(A)^{k+1}-\epsilon is syndetic. The size of this set, surprisingly enough, depends on the length (k+1) of the arithmetic progression under consideration. In an ergodic system, for k=2 and k=3, this set is syndetic, while for kòf(x)f(Tⁿx)f(T²ⁿx)? f(T^knx)  dm(x)\int{f(x)f(T^{n}x)f(T^{2n}x){\ldots} f(T^{kn}x) \,d\mu(x)} , where k and n are positive integers and f is a bounded measurable function. We also derive combinatorial consequences of these results, for example showing that for a set of integers E with upper Banach density d^*(E)>0 and for all {n ? \mathbbZ\colon d^*(E?(E+n)?(E+2n)?(E+3n)) > d^*(E)⁴-e}\big\{n\in\mathbb{Z}{\colon} d^*\big(E\cap(E+n)\cap(E+2n)\cap(E+3n)\big) > d^*(E)^4-\epsilon\big\}     

Inverse gas chromatography of lignocellulosic fibers coated with a thermosetting polymer: Use of peak maximum and conder and young methods

The Conder and Young (CY) and the peak maximum (PM) methods were used to estimate the retention time of n-alkane probes on chemithermomechanical pulp (CTMP) wood fibers treated with a low molecular weight grade phenol-formaldehyde resin (PFR). Thermodynamic functions (ΔH_a^o, ΔG_a^o, and ΔS_a^o) and the London dispersive component of the surface energy were derived from these retention times. Treated wood fibers show a high energy surface due to the presence of the thermoset resin on their surface. Values of ΔH_a^o obtained from the CY method were higher than those obtained with the PM method at relatively high temperatures and with relatively low molecular weight alkanes. The results from the two methods were identical at low temperature (293 K) and with the relatively high molecular weight alkane n-undecane.     

Photothermal microanalysis of thermal discontinuities in metallic samples

Modeling the behavior of a protective coating during a thermal shock not only requires the knowledge of its own thermophysical characteristics, but also those of the coating–substrate discontinuity. According to its nature, this discontinuity can be modeled as a zero-thickness interface (thermal contact resistance) or a finite thickness layer (thermal third body). This paper presents an experimental device and two associated thermal transfer models developed in view of the microscale characterization of such discontinuities.     

Convergence of interval-type algorithms for generalized fractional programming

The purpose of this paper is to analyze the convergence of interval-type algorithms for solving the generalized fractional program. They are characterized by an interval [LB _k , UB _k ] including*, and the length of the interval is reduced at each iteration. A closer analysis of the bounds LB _k and UB _k allows to modify slightly the best known interval-type algorithm NEWMODM accordingly to prove its convergence and derive convergence rates similar to those for a Dinkelbach-type algorithm MAXMODM under the same conditions. Numerical results in the linear case indicate that the modifications to get convergence results are not obtained at the expense of the numerical efficiency since the modified version BFII is as efficient as NEWMODM and more efficient than MAXMODM.This research was supported by NSERC (Grant A8312) and FCAR (Grant 0899).     

Synthesis of 3-formyltetronic acid and enamine derivatives

The first reported synthesis of 3-formyltetronic acid and its conversion to enamine derivatives is described. 3-Dimethylaminomethylene-2,4-dioxotetrahydrofuran derivatives were also prepared by treatment of tetronic acids with dimethylformamide diethyl acetal. Nmr spectral studies are included.     

(1-Adamantanethio)pyridines and tetrahydropyridines from the reaction of 1-adamantanethiol with pyridine I-oxide in acetic anhydride

The reaction of pyridine 1-oxide with 1-adamantanethiol in acetic anhydride produced a mixture of 2- and 3-(1-adamantanethio)pyridines, 1-aeetyl-2-(1-adamantanethio)-3-hydroxy-4-acetoxy-1,2,3,4-telrahydropyridine and the corresponding 3-acetoxyderivative. Pure substances were separated by means of column chromatography on alumina. The tetrahydropyridines were identified by means of their proton magnetic and mass spectra. 4-(1-Adamantanethio)pyridine was synthesized from 4-chloropyridinc and 1-adamantanethiol. The three isomeric (1-adamantanethio)-pyridines were, each, cleaved by concentrated hydrochloric acid to give 1-chloroadamantane and the corresponding pyridinethiol.