In Defense of the Bankruptcy Code\u27s Radical Integration of the Preference Rules Affecting Commercial Financing

The passage of the Bankruptcy Reform Act of 1978 significantly changed the statutory foundation of American preference law. Section 547 mixes new, carefully measured concepts with familiar definitional language from old section 60. The new conceptual structure of section 547 is a departure from the abstract framework of its predecessor. Under section 60, worthy transfers were protected by qualifications imaginatively grafted by the judges onto the specific elements of the preference definition. Among the most ingenious, and perhaps most significant, of these qualifications were those designed to protect pre-petition transfers incident to various types of financing arrangements. In contrast, section 547 of the Bankruptcy Code (Code) is a new and radical integration of definition and exception. The exceptions are separately listed in the statute and are not codifications of old case law qualifications. The new statutory test clearly displaces the old approach to worthy transfers. The use of section 60 language in the 547(b) definition of a preference, however, makes the vitality of old case law qualifications of this language an open question. The role of this case law in the new integration is a general concern that runs throughout the following discussion. Another general concern is the mechanics of the new integration when transfers normally incident to commercial financing are involved. What is the proper relationship between definition and exception in the new integration? How do the separate exceptions which may affect commercial financing relate to one another? Although the language of each exception suggests an isolated application, in a typical commercial financing arrangement several exceptions may be brought into play. This Article systematically examines the many specific problems within these broad topic areas in an effort to provide helpful solutions

Using NLP technology in CALL

This paper outlines the research and guiding research principles of the (I)CALL group at Dublin City University, Ireland. Our research activities include the development of (I)CALL systems targeted at a variety of user groups including advanced Romance language learners, intermediate to advanced German learners, primary and secondary school students as well as students with L1 learning disabilities requiring a variety of system types which cater to individual user needs and abilities. Suitable CL/NLP technology is incorporated where appropriate for the learner

Formation and structural chemistry of the unusual cyanide-bridged dinuclear species [Ru-2(NN)(2)(CN)(7)](3-)(NN=2,2 '-bipyridine or 1,10-phenanthroline)

Crystallisation of simple cyanoruthenate complex anions [Ru(NN)(CN)(4)](2) (NN = 2,2'-bipyridine or 1,10-phenanthroline) in the presence of Lewis-acidic cations such as Ln(III) or guanidinium cations results, in addition to the expected [Ru(NN)(CN)(4)](2) salts, in the formation of small amounts of salts of the dinuclear species [Ru-2(NN)(2)(CN)(7)](3). These cyanide-bridged anions have arisen from the combination of two monomer units [Ru(NN)(CN)(4)](2) following the loss of one cyanide, presumably as HCN. The crystal structures of [Nd(H2O)(5.5)][Ru-2(bipy)(2)(CN)(7)] center dot 11H(2)O and [Pr(H2O)(6)][Ru-2(phen)(2)(CN)(7)] center dot 9H(2)O show that the cyanoruthenate anions form Ru-CN-Ln bridges to the Ln(III) cations, resulting in infinite coordination polymers consisting of fused Ru(2)Ln(2)(mu-CN)(4) squares and Ru(4)Ln(2)(mu-CN)(6) hexagons, which alternate to form a one-dimensional chain. In [CH6N3](3)[Ru-2(bipy)(2)(CN)(7)] center dot 2H(2)O in contrast the discrete complex anions are involved in an extensive network of hydrogen-bonding involving terminal cyanide ligands, water molecules, and guanidinium cations. In the [Ru-2(NN)(2)(CN)(7)](3) anions themselves the two NN ligands are approximately eclipsed, lying on the same side of the central Ru-CN-Ru axis, such that their peripheries are in close contact. Consequently, when NN = 4,4'-Bu-t(2)-2,2'-bipyridine the steric bulk of the t-butyl groups prevents the formation of the dinuclear anions, and the only product is the simple salt of the monomer, [CH6N3](2)[Ru((t)Bu(2)bipy)(CN)(4)] center dot 2H(2)O. We demonstrated by electrospray mass spectrometry that the dinuclear by-product [Ru-2(phen)(2)(CN)(7)](3) could be formed in significant amounts during the synthesis of monomeric [Ru(phen)(CN)(4)](2) if the reaction time was too long or the medium too acidic. In the solid state the luminescence properties of [Ru-2(bipy)(2)(CN)(7)](3) (as its guanidinium salt) are comparable to those of monomeric [Ru(bipy)(CN)(4)](2), with a (MLCT)-M-3 emission at 581 nm

Integral Neutron Multiplicity Measurements from Cosmic Ray Interactions in Lead

Sixty element 3He neutron multiplicity detector systems were designed, constructed and tested for use in cosmic ray experiments with a 30-cm cube lead target. A series of measurements were performed for the cosmic ray configuration at ground level (3 meters water equivalent, mwe), in the St. Petersburg metro tunnel (185 mwe), and in the Pyhäsalmi mine in Finland (583 and 1185 mwe). Anomalous coincidence events with charged cosmic ray particles at sea level produced events with 100-120 neutrons due possibly to the total disintegration of the Pb nucleus. These events were also detected at 185 mwe, but the particles causing such disintegration are currently unidentified. We present examples of preliminary data from the various measurements and discuss future plans for underground experiments including possible searches for Weakly Interacting Massive Particles (WIMP, dark matter)