Cost optimization of cross-laminated timber panels in one-way bending

European Journal of Wood and Wood Products - For the purposes of structural design, cross-laminated timber (CLT) panels are typically chosen from tables detailing standardized layups. While this is...     

Covalently-Bonded “Onion Type” Double Fullerenic Carbon Cages

Abstract

Three “onion type” double carbon cages (consisting of an inner sp³-hybridized C₆₀ buckminsterfullerene skeleton and an outer larger carbon cage with icosahedral symmetry, with covalent bonds between the carbon atoms of the 5-membered rings) are described and their strain energies are discussed: (i) when the outer cage is a C₁₂₀ cage derived from buckminsterfullerene by replacing each bond between two six-membered rings by an acetylenic group, the strain is smallest.; (ii) when the same derivation concerns each bond between 5- and 6-membered rings leading to a C₁₈₀ outer cage, the strain is largest.; (iii) when the outer cage is C₁₈₀ with benzenoid rings, the strain is intermediate.     

Dependence of conductivity of an illuminated nonideal heterojunction on external bias

The possibility of using a model of the tunnel-hopping charge transport to calculate the conductivity in the barrier region of the illuminated nonideal heterojunction is shown. The current-voltage characteristics of the heterojunction was calculated taking into account the prevalence of the tunnel-hopping transport mechanism in the barrier region and the change in the potential barrier shape upon exposure to light. It is shown that the current-voltage characteristics of such a heterojunction calculated at various illumination intensities are in good agreement with those observed experimentally.     

Phonological universals constrain the processing of nonspeech stimuli.

Domain-specific systems are hypothetically specialized with respect to the outputs they compute and the inputs they allow (Fodor, 1983). Here, we examine whether these 2 conditions for specialization are dissociable. An initial experiment suggests that English speakers could extend a putatively universal phonological restriction to inputs identified as nonspeech. A subsequent comparison of English and Russian participants indicates that the processing of nonspeech inputs is modulated by linguistic experience. Striking, qualitative differences between English and Russian participants suggest that they rely on linguistic principles, both universal and language-particular, rather than generic auditory processing strategies. Thus, the computation of idiosyncratic linguistic outputs is apparently not restricted to speech inputs. This conclusion presents various challenges to both domain-specific and domain-general accounts of cognition. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Real-time cardiac MRI using DSPs

A real-time cardiac magnetic resonance imaging (MRI) system has been implemented using digital signal processing (DSP) technology. The system enables real-time acquisition, processing, and display of ungated cardiac movies at moderate video rates of 20 images/s. A custom graphical user interface (GUI) provides interactive control of data acquisition parameters and image display functions. Images can be compressed into moving-picture experts group (MPEG) movies, but are displayed on the console without compression during the scan. Compared to existing real-time MRI systems, implementation with DSP's allows rapid parallel computations, fast data transfers, and greater system flexibility, including the ability to scale to multiple channels, at the expense of somewhat higher component cost.     

PARTITIONING OF π-ELECTRONS IN RINGS OF POLYCYCLIC conjugated HYDROCARBONS. PART 1: CATACONDENSED BENZENOIDS

Recently a novel view on Kekulé valence structures (or resonance structures) was reported in which their standard geometrical representation was replaced by a numerical representation obtained by assigning π-electrons associated with CC double bonds to individual benzenoid rings. In the present article, we examine in more detail the partitioning of π-electrons to benzenoid rings for cata-condensed benzenoid hydrocarbons. For special families of cata-condensed benzenoids, we offer formulas which allow one to obtain the average π-electron ring content for individual benzenoid rings of polycyclic conjugated hydrocarbons. We also show that the average π-electron ring content for individual benzenoid rings can be calculated from Pauling bond orders without a need to examine all Kekulé resonance structures of a molecule.