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1.
We develop a scenario in which feeble intermediate range forces emerge as an effect resulting from the compactification (à la Kaluza-Klein) of multidimensional theories. These feeble forces compete with gravity and in general permit different bodies to fall to earth with different accelerations. We show that these feeble forces are mediated by vectors (V) and/or scalars (S), whose dimensionless coupling constants are typically of order gv gs 10–10 Under certain plausible assumptions the ranges of these feeble forces are expected to be of order 1 m to 1 km. It is conjectured that the general strategy will prove applicable to realistic multidimensional theories such as the 10-dimensional superstring theories. We speculate that deviations from the standard gravitational force-similar to the ones reported recently as a fifth force-may be interpreted as evidence for higher dimensions.This essay received the second award from the Gravity Research Foundation for the year 1986.Supported by the U.S. Department of Energy under grant # DE-FG03-84ER-40168.  相似文献   
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Low permittivity ceramic substrates with a sandwich structure consisting of a porous, fiber-reinforced SiO2 core and two thin polymer plates were fabricated by sol-gel processing, and polymer infiltration. The rheological behavior of an aqueous colloidal SiO2 sol, containing short SiO2 fibers was studied as a function of particle loading, fiber loading and gelation time. Short SiO2 fibers were introduced to limit drying shrinkage and thus minimize substrate cracking during drying. After the psuedoplastic sol was tape cast and sintered at 1150°C for 2 h, a polyimide solution was infiltrated into the porous SiO2 core. Permittivities ranging from 1.81 to 3.08 could be obtained by using 32–42% SiO2, 5–50% polyimide and 63 to 8% porosity. The substrate strength was increased from 1.93 MPa to 3.83 MPa after polyimide infiltration.  相似文献   
3.
Monodispersed poly(4-bromostyrenes) (PBs) and their block copolymers with styrene, isoprene, and 3-methylbutene were prepared and characterized by GPC and NMR. Polystyryl and α-methylstyryl carbanions act as effective initiators of the anionic polymerization of Bs in THF. The undersirable side reactions, due to thermally or photochemically induced decomposition of the bromostyryl carbanions, PBs?, may be eliminated by conducting the reaction at ?78°C and in the dark. Under such conditions, the rate constant of propagation, kp (?78°), is 1.5 × 103 M?1 s?1. Radical anions, \documentclass{article}\pagestyle{empty}\begin{document}$ {\rm Bs}^{\mathop - \limits_ \cdot} $\end{document}, formed as result of electron transfer from sodium naphthalenide to Bs, may eject spontaneously bromine ions. This step and reactions involving the respective phenyl radicals compete at ?78°C with the addition steps leading to polymer formation. Electron affinity of Bs seems to be much higher than that of styrene or isoprene, and PBs? carbanions do not add to the latter monomers. Addition of Bs to polyisoprenyl carbanions leads to formation of the BsIBs block copolymers. BsIBs, prepared in THF, may be converted by preferential hydrogenation of the 1–2 adducts into block copolymers of Bs with poly(2-methylbutene) and isoprenyl segments. The effectiveness of Bs as a flame retarding constituent of polymeric systems seems to be much more pronounced when it is incorporated in a “block” than in a random fashion. A considerably larger fraction of PBs is required to achieve the same LOI value when the respective homopolymers are blended. Spatial distribution of the easily charred microdomains in the block copolymers is believed to be responsible for this phenomenon.  相似文献   
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In this paper we report the results of an experimental study of the vacuum ultraviolet absorption spectra of molecular impurity states of methyl iodide in Ar (density range ? = 0–1.4 g cm?3) and in Kr (? = 0–2.3 g cm?3), of carbon disulphide in Ar (? = 0–1.4 g cm?3) and of formaldehyde in Ar (? = 0–1.25 g cm?3). The experimental results provide new information regarding medium perturbations of intravalenc transitions, of the lowest extravalence transitions and of transitions to mixed valence—Rydberg configurations, which serve as a diagnostic tool to distinguish between different types of electronic excitations. All the lowest extravalence molecular excitations exhibit appreciable blue spectral shifts at moderate and at high fluid densities, intravalence transitions are practically insensitive to medium effects, while excitations to mixed valence—Rydberg configurations are characterized by a moderate blue spectral shift. New information has been obtained concerning the energetics of molecular ionization processes in a dense fluid. The high n = 2–5 Rydberg states of CH3l exhibit a large red shift at moderate (? = 0–0.5 cm?3) Ar densities. The ionization potential Eg and the effective Rydberg constant G for CH3I in Ar was found to decrease from G = 13.6 eV and Eg = 9.55 eV at ? = 0 and Eg = 9.08 eV and constant G for CH3l in Ar was found to decrease from G = 13.6 eV and Eg = 9.55eV at ? = 0 and Eg = 9.08 eV and G ≈ 7.15 eV at ? = 0.5 g cm?3. Experimental evidence was obtained for the identification of n = 2 molecular Wannier impurity states of CH3I and of CH2O in liquid Ar. These spectroscopic data result in Eg ≈ 8.6 eV for CH3I in liquid Ar and Eg ≈ 10.2 eV for CH2O in liquid Ar.  相似文献   
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Superstrings have been proposed as a quantum-theoretical framework for unifying all the fundamental forces, including gravity. We consider the question of whether there might be more general supersymmetric possibilities, based on higher extended objects such as membranes, jellies, etc. We argue that all the possible extended objects in all possible spacetime dimensions are quantummechanically inconsistent except for the 10-dimensional superstring and the 11-dimensional supermembrane. These are also the only two such theories that contain massless gravitons and, thus, that can describe gravity at low energies. It is remarkable that the range of possibilities can be narrowed down to this extent. Whether these can be further narrowed down to just one consistent theory remains open to further research.This essay received the first award from the Gravity Research Foundation for the year 1988.-Ed.  相似文献   
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The intensive use of nano-sized titanium dioxide (TiO2) particles in many different applications necessitates studies on their risk assessment as there are still open questions on their safe handling and utilization. For reliable risk assessment, the interaction of TiO2 nanoparticles (NP) with biological systems ideally needs to be investigated using physico-chemically uniform and well-characterized NP. In this article, we describe the reproducible production of TiO2 NP aerosols using spark ignition technology. Because currently no data are available on inhaled NP in the 10?C50 nm diameter range, the emphasis was to generate NP as small as 20 nm for inhalation studies in rodents. For anticipated in vivo dosimetry analyses, TiO2 NP were radiolabeled with 48V by proton irradiation of the titanium electrodes of the spark generator. The dissolution rate of the 48V label was about 1% within the first day. The highly concentrated, polydisperse TiO2 NP aerosol (3?C6 × 106 cm?3) proved to be constant over several hours in terms of its count median mobility diameter, its geometric standard deviation, and number concentration. Extensive characterization of NP chemical composition, physical structure, morphology, and specific surface area was performed. The originally generated amorphous TiO2 NP were converted into crystalline anatase TiO2 NP by thermal annealing at 950 °C. Both crystalline and amorphous 20-nm TiO2 NP were chain agglomerated/aggregated, consisting of primary particles in the range of 5 nm. Disintegration of the deposited TiO2 NP in lung tissue was not detectable within 24 h.  相似文献   
10.
A generalization of the static shakedown theorems for elastic plastic hardening solids with isotropic [Mech. Res. Commun. 29 (2002) 159] and anisotropic [Acta Mechanica, 2004] damage accounting for the possibility of material softening is proposed.  相似文献   
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