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91.
Diederik Aerts Bart D’Hooghe Emmanuel Haven 《International Journal of Theoretical Physics》2010,49(12):2971-2990
We prove a theorem which shows that a collection of experimental data of probabilistic weights related to decisions with respect
to situations and their disjunction cannot be modeled within a classical probabilistic weight structure in case the experimental
data contain the effect referred to as the ‘disjunction effect’ in psychology. We identify different experimental situations
in psychology, more specifically in concept theory and in decision theory, and in economics (namely situations where Savage’s
Sure-Thing Principle is violated) where the disjunction effect appears and we point out the common nature of the effect. We
analyze how our theorem constitutes a no-go theorem for classical probabilistic weight structures for common experimental
data when the disjunction effect is affecting the values of these data. We put forward a simple geometric criterion that reveals
the non classicality of the considered probabilistic weights and we illustrate our geometrical criterion by means of experimentally
measured membership weights of items with respect to pairs of concepts and their disjunctions. The violation of the classical
probabilistic weight structure is very analogous to the violation of the well-known Bell inequalities studied in quantum mechanics.
The no-go theorem we prove in the present article with respect to the collection of experimental data we consider has a status
analogous to the well known no-go theorems for hidden variable theories in quantum mechanics with respect to experimental
data obtained in quantum laboratories. Our analysis puts forward a strong argument in favor of the validity of using the quantum
formalism for modeling the considered psychological experimental data as considered in this paper. 相似文献
92.
Prof. Dr. Karen Hemelsoet Qingyun Qian Thierry De Meyer Kristof De Wispelaere Dr. Bart De Sterck Prof. Dr. Bert M. Weckhuysen Prof. Dr. Michel Waroquier Prof. Dr. Veronique Van Speybroeck 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(49):16595-16606
The optical absorption properties of (poly)aromatic hydrocarbons occluded in a nanoporous environment were investigated by theoretical and experimental methods. The carbonaceous species are an essential part of a working catalyst for the methanol‐to‐olefins (MTO) process. In situ UV/Vis microscopy measurements on methanol conversion over the acidic solid catalysts H‐SAPO‐34 and H‐SSZ‐13 revealed the growth of various broad absorption bands around 400, 480, and 580 nm. The cationic nature of the involved species was determined by interaction of ammonia with the methanol‐treated samples. To determine which organic species contribute to the various bands, a systematic series of aromatics was analyzed by means of time‐dependent density functional theory (TDDFT) calculations. Static gas‐phase simulations revealed the influence of structurally different hydrocarbons on the absorption spectra, whereas the influence of the zeolitic framework was examined by using supramolecular models within a quantum mechanics/molecular mechanics framework. To fully understand the origin of the main absorption peaks, a molecular dynamics (MD) study on the organic species trapped in the inorganic host was essential. During such simulation the flexibility is fully taken into account and the effect on the UV/Vis spectra is determined by performing TDDFT calculations on various snapshots of the MD run. This procedure allows an energy absorption scale to be provided and the various absorption bands determined from in situ UV/Vis spectra to be assigned to structurally different species. 相似文献
93.
The covering spectrum is a geometric invariant of a Riemannian manifold, more generally of a metric space, that measures the size of its one-dimensional holes by isolating a portion of the length spectrum. In a previous paper we demonstrated that the covering spectrum is not a spectral invariant of a manifold in dimensions three and higher. In this article we give an example of two isospectral Cayley graphs that admit length space structures with distinct covering spectra. From this we deduce the existence of infinitely many pairs of Sunada-isospectral surfaces with unequal covering spectra. 相似文献
94.
95.
96.
In this work, a novel flow-through solid-phase based chemiluminescence (CL) optical sensor is described for the trace determination of orthophosphate in waters exploiting the multisyringe flow injection analysis (MSFIA) concept with multicommutation. The proposed time-based injection flow system relies upon the in-line derivatisation of the analyte with ammonium molybdate in the presence of vanadate, and the transient immobilisation of the resulting heteropolyacid in a N-vinylpyrrolidone/divinylbenzene copolymer packed spiral shape flow-through cell located in front of the window of a photomultiplier tube. The simultaneous injection of well-defined slugs of luminol in alkaline medium and methanol solution towards the packed reactor is afterwards performed by proper switching of the solenoid valves. Then, the light emission from the luminol oxidation by the oxidant species retained onto the sorbent material is readily detected. At the same time, the generated molybdenum-blue compound is eluted by the minute amount of injected methanol, rendering the system prepared for a new measuring cycle. Therefore, the devised sensor enables the integration of the solid-phase CL reaction with elution and detection of the emitted light without the typical drawbacks of the molybdenum-blue based spectrophotometric procedures regarding the excess of molybdate anion, which causes high background signals due to its self-reduction. The noteworthy features of the developed CL-MSFIA system are the feasibility to accommodate reactions with different pH requirements and the ability to determine trace levels of orthophosphate in high silicate content samples (Si/P ratios up to 500). Under the optimised conditions, a dynamic linear range from 5 to 50 μg P l−1 for a 1.8 ml sample, repeatability better than 3.0% and a quantification limit of 4 μg P l−1 were attained. The flowing stream system handles 11 analysis h−1 and has been successfully applied to the determination of trace levels of orthophosphate in environmental samples such as mineral, ground, tap and pond waters as well as samples from a water-steam cycle of an incineration plant. The t-test comparison of the means for the developed optical sensor and the molybdenum-blue spectrophotometric APHA/AWWA/WPCF reference method revealed that there is no evidence of significant differences between the obtained results at the 95% confidence level. 相似文献
97.
98.
Imre Bucsi Szabolcs Cserényi Károly Felf?ldi Mihály Bartók 《Reaction Kinetics and Catalysis Letters》2006,87(2):281-289
Summary We synthesized C9-O-silyl ethers of cinchonidine and dihydrocinchonidine (1-8), seven of which have not been known before. The structures of the compounds were verified by ESI-ion-trap MS and 1H-NMR. Fragmentation of silyl ethers containing Si-phenyl bonds was studied for the first time. The compounds obtained will
be utilized as chiral catalysts of certain asymmetric syntheses.</o:p> 相似文献
99.
Antonino Mazzaglia Luigi Monsu' Scolaro Raphael Darcy Ruth Donohue Bart Jan Ravoo 《Journal of inclusion phenomena and macrocyclic chemistry》2002,44(1-4):127-132
The entanglement process between porphyrins and some amphiphiliccyclodextrins and the occurrence of different species have been proved by the combination of UV-Visabsorption, fluorescence anisotropy, resonance light scattering and 1H NMR spectroscopy. 相似文献
100.