The use of hydrogen peroxide as a precursor to improvised explosives has made its detection a topic of critical importance. Chemiresistor arrays comprised of 50 nm thick films of metallophthalocyanines (MPcs) are redox selective vapor sensors of hydrogen peroxide. Hydrogen peroxide is shown to decrease currents in cobalt phthalocyanine sensors while it increases currents in nickel, copper, and metal-free phthalocyanine sensors; oxidation and reduction of hydrogen peroxide via catalysis at the phthalocyanine surface are consistent with the pattern of sensor responses. This represents the first example of MPc vapor sensors being oxidized and reduced by the same analyte by varying the metal center. Consequently, differential analysis by redox contrast with catalytic amplification using a small array of sensors may be used to uniquely identify peroxide vapors. Metallophthalocyanine chemiresistors represent an improvement over existing peroxide vapor detection technologies in durability and selectivity in a greatly decreased package size. 相似文献
We develop a cohomological method to classify amalgams of groups. We generalize this to simplicial amalgams in any concrete category. We compute the non-commutative 1-cohomology for several examples of amalgams defined over small simplices. 相似文献
The paper introduces a novel procedure to determine the non-linear parameter of the Giesekus model, in relation to the characterization of the non-linear oscillatory shear regime of viscoelastic polymer solutions based on polyacrylamide. Instead of using the shear-thinning viscosity as the representative non-linear effect, the third harmonic in the Fourier spectrum of the shear stress response signal is considered for computing the mobility factor. The fluid is subjected to large amplitude oscillatory shear (LAOS) and its response is recorded. Deviations of this signal from the sinusoidal form are specific to each material and gives both qualitative and quantitative measures of the non-linearity. By fitting the material response with the corresponding numerical solutions of the n-modes Giesekus constitutive relation, one can extract the values of the non-linear αi-parameters that describe the fluid rheology. It is demonstrated that this procedure, which can be successfully applied to semi-concentrated polymer solutions, provides better results than the classical viscosity-fit method. 相似文献
Crucial breakthroughs in the activation of the C(aryl)? O bond of phenol derivatives were achieved almost simultaneously by two research groups (see scheme; Cy=cyclohexyl). Garg et al. coupled a range of aryl pivalates with arylboronic acids to give unsymmetrical biaryls. Shi et al. achieved this through C(aryl)? O activation of aryl carboxylates; the best results for the coupling of aryl boroxines were again obtained with aryl pivalates.
Digital image correlation (DIC) has seen widespread acceptance and usage as a non-contact method for the determination of full-field displacements and strains in experimental mechanics. The advances of imaging hardware in the last decades led to high resolution and speed cameras being more affordable than in the past making large amounts of data image available for typical DIC experimental scenarios. The work presented in this paper is aimed at maximizing both the accuracy and speed of DIC methods when employed with such images. A low-level framework for speckle image partitioning which replaces regularly shaped blocks with image-adaptive cells in the displacement calculation is introduced. The Newton-Raphson DIC method is modified to use the image pixels of the cells and to perform adaptive regularization to increase the spatial consistency of the displacements. Furthermore, a novel robust framework for strain calculation based also on the Newton-Raphson algorithm is introduced. The proposed methods are evaluated in five experimental scenarios, out of which four use numerically deformed images and one uses real experimental data. Results indicate that, as the desired strain density increases, significant computational gains can be obtained while maintaining or improving accuracy and rigid-body rotation sensitivity. 相似文献
The synthesis and characterization of several ipso-functionalized derivatives of the bulky terphenyl group are described. These include the primary alcohol Ar′CH2OH (1), the bromo derivative Ar′CH2Br (2), and the terphenyl formate Ar′CH2OC(O)H (3). The alcohol 1 was obtained by treatment of LiAr′ with formaldehyde, and 1 was readily converted to the bromo derivative 2 using HBr. The reaction of 1 with formic acid afforded 3 in good yield. Attempts to form the Grignard derivative of 1, i.e., Ar′CH2MgBr, resulted in a head-to-tail reaction of the terphenyl benzyl units to yield an unusual coupled product 4. An approach to the avoidance of this coupling involved the synthesis of the terphenyl derivatives and , bearing methyl groups in the para positions of the central aryl ring, which could be prepared in good yield, and converted to their respective lithium salts 7 and 8 without complication . The compounds were characterized by 1H and 13C NMR spectroscopy, IR spectroscopy (1) and X-ray crystallography (2, 4, 5 and 6). 相似文献
New polyesters were prepared from several aromatic phosphonic dichlorides and a diolic monomer bearing a cyclic bulky group containing phosphorus. From kinetic investigation, the rates of polycondensation in melt were calculated and compared with those of the reaction between aromatic diols and phosphonic dichloride. Polyesters were analytically, spectral and thermally characterized and effect of structure on optical properties was investigated. 相似文献
Kinetic, isotopic, and infrared studies on well-defined dispersed Pt clusters are combined here with first-principle theoretical methods on model cluster surfaces to probe the mechanism and structural requirements for CO oxidation catalysis at conditions typical of its industrial practice. CO oxidation turnover rates and the dynamics and thermodynamics of adsorption-desorption processes on cluster surfaces saturated with chemisorbed CO were measured on 1-20 nm Pt clusters under conditions of strict kinetic control. Turnover rates are proportional to O(2) pressure and inversely proportional to CO pressure, consistent with kinetically relevant irreversible O(2) activation steps on vacant sites present within saturated CO monolayers. These conclusions are consistent with the lack of isotopic scrambling in C(16)O-(18)O(2)-(16)O(2) reactions, and with infrared bands for chemisorbed CO that did not change within a CO pressure range that strongly influenced CO oxidation turnover rates. Density functional theory estimates of rate and equilibrium constants show that the kinetically relevant O(2) activation steps involve direct O(2)* (or O(2)) reactions with CO* to form reactive O*-O-C*=O intermediates that decompose to form CO(2) and chemisorbed O*, instead of unassisted activation steps involving molecular adsorption and subsequent dissociation of O(2). These CO-assisted O(2) dissociation pathways avoid the higher barriers imposed by the spin-forbidden transitions required for unassisted O(2) dissociation on surfaces saturated with chemisorbed CO. Measured rate parameters for CO oxidation were independent of Pt cluster size; these parameters depend on the ratio of rate constants for O(2) reactions with CO* and CO adsorption equilibrium constants, which reflect the respective activation barriers and reaction enthalpies for these two steps. Infrared spectra during isotopic displacement and thermal desorption with (12)CO-(13)CO mixtures showed that the binding, dynamics, and thermodynamics of CO chemisorbed at saturation coverages do not depend on Pt cluster size in a range that strongly affects the coordination of Pt atoms exposed at cluster surfaces. These data and their theoretical and mechanistic interpretations indicate that the remarkable structure insensitivity observed for CO oxidation reactions reflects average CO binding properties that are essentially independent of cluster size. Theoretical estimates of rate and equilibrium constants for surface reactions and CO adsorption show that both parameters increase as the coordination of exposed Pt atoms decreases in Pt(201) cluster surfaces; such compensation dampens but does not eliminate coordination and cluster size effects on measured rate constants. The structural features and intrinsic non-uniformity of cluster surfaces weaken when CO forms saturated monolayers on such surfaces, apparently because surfaces and adsorbates restructure to balance CO surface binding and CO-CO interaction energies. 相似文献