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A general principle of causal duality for physical systems, lying at the base of representation theorems for both compound and evolving systems, is proved; formally it is encoded in a quantaloidal setting. Other particular examples of quantaloids and quantaloidal morphisms appear naturally within this setting; as in the case of causal duality, they originate from primitive physical reasonings on the lattices of properties of physical systems. Furthermore, an essentially dynamical operational foundation for studying physical systems is outlined; complementary as it is to the existing static operational foundation, it leads to the natural axiomatization of causal duality in operational quantum logic.  相似文献   
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Eight groups of chinchillas (N=74) were exposed to various equivalent energy [100 or 106 dB(A) sound pressure level (SPL)] noise exposure paradigms. Six groups received an interrupted, intermittent, time varying (IITV) Gaussian noise exposure that lasted 8 h/d, 5 d/week for 3 weeks. The exposures modeled an idealized workweek. At each level, three different temporal patterns of Gaussian IITV noise were used. The 100 dB(A) IITV exposure had a dB range of 90-108 dB SPL while the range of the 106 dB(A) IITV exposure was 80-115 dB SPL. Two reference groups were exposed to a uniform 100 or 106 dB(A) SPL noise, 24 h/d for 5 days. Each reference group and the three corresponding IITV groups comprised a set of equivalent energy exposures. Evoked potentials were used to estimate hearing thresholds and surface preparation histology quantified sensory cell populations. All six groups exposed to the IITV noise showed threshold toughening effects of up to 40 dB. All IITV exposures produced hearing and sensory cell loss that was similar to their respective equivalent energy reference group. These results indicate that for Gaussian noise the equal energy hypothesis for noise-induced hearing loss is an acceptable unifying principle.  相似文献   
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A new metal-organic complex [Mn2(PDC)2(bipy)2(H2O)2] (H2PDC = 2,4-pyridine-dicarboxylic acid, bipy = 2,2′-bipyridine) 1 has been hydrothermally synthesized and structurally characterized by elemental analysis, IR spectrum, TG and single-crystal X-ray diffraction. The compound crystallizes in triclinic, space group P ^-1 with a = 7.376(3), b = 9.990(4), c = 11.950(5) A^°, α= 75.217(5), β = 78.052(5), γ = 70.655(5)°, V = 796.0(5)A^°3, C34HE6Mn2N6O10, Mr = 788.49, De = 1.645 g/cm^3,μ(MoKa) = 0.866 mm^-1, F(000) = 235, Z = 1, the final R = 0.0425 and wR = 0.0700 for 1971 observed reflections (I 〉 2σ(I)). In the crystal structure, the manganese atom is six-coordinated by two carboxylate oxygen atoms from two different PDC ligands, one aqua ligand, and three nitrogen atoms from 2,2′-bipy and PDC ligands, giving a distorted octahedral geometry. It exhibits a three-dimensional supramolecular network defined by O-H…O hydrogen-bonding interactions.  相似文献   
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The effects of cationic polyethylenimine (PEI) on the colloidal stability of anionic fines (microcrystalline cellulose or thermomechanical fines), fillers (clay) and their mixtures in deionized and tap water were investigated, using a photometric dispersion analyzer. Measurements confirmed that PEI flocculates all used materials by charge neutralization. As expected, higher additions of PEI lead to electrostatic stabilization of microcellulose and clay suspensions, but it was not possible to stabilize the suspension of fines using high additions of PEI. This is ascribed to the mechanical entanglements of fibrillar fines. In tap water, much more PEI is needed to reach optimum flocculation conditions than in deionized water. Heteroflocculation between PEI-coated clay and fines takes place with a rate which, for high fines concentration and a constant clay concentration, is independent of fines concentration. A theoretical model for the heteroflocculation of fines with PEI-coated clay has been developed, which explains the observed trends. In essence, clay particles can act as bridging agents for fines flocculation.  相似文献   
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Mineral and short-chain carboxylic acid vapours and NO(x) gases were reacted with cyclohexene oxide (1,2-epoxycyclohexane) to quantitatively produce specific, thermally stable cyclohexyl derivatives. Subsequent analysis of these derivatives by gas chromatography with mass spectroscopy and flame ionisation detection afforded a multi analyte method for the assay of these gaseous acidic atmospheric species. Derivatisation was found to be quantitative for the derivatives tested and the method highly sensitive (to 0.3 mg/m3 for a 30 l sample), accurate, precise and free from apparent interferences. The technique has been applied to "acid stack gases" and a number of other acid rich atmospheres and the results obtained show good agreement with the single analyte wet chemical determinations indicating that the approach has considerable potential as a routine analytical method for measuring such atmospheric pollutants. The high specificity of the reaction mechanism and its potential for the analysis of analyte mixtures is illustrated in the assay of nitric acid and its acid anhydride, dinitrogen pentoxide.  相似文献   
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