A categorical characterization of varieties

A simple, direct proof of the following characterization of varieties of (finitary) algebras is presented: a cocomplete category is equivalent to a variety iff it has an algebraic generator, i.e., a regular generator which is exactly projective and finitely generated. This improves somewhat a recent restatement, due to Pedicchio and Wood, of the classical characterization theorem of Lawvere. A bijective correspondence between algebraic theories and algebraic generators is established.     

On essential extensions of reduced rings and domains

A ring is said to be a left essential extension of a reduced ring (domain) if it contains a left ideal which is a reduced ring (domain) and intersects nontrivially every nonzero twosided ideal of the ring. We prove that every ring which is a left essential extension of a reduced ring is a subdirect sum of rings which are essential extensions of domains, but the converse implication does not hold. We give some applications of this result and discuss several related questions.Received: 6 January 2003     

Chemical Mechanisms of Liquid–Liquid and Solid-Phase Extraction of Metal Chelates

Conditions of the liquid–liquid and solid-phase extraction of metal chelates are compared. The analogy and differences in the behavior of chelates and the effect of stability and partition constants on the completeness of the extraction of metals are discussed.     

Covering group and graph of discretized volumes

We consider a discretized volume V consisting of finite, congruent and attached copies of a tile t. We find a group L _V the orbit of which, when applied to t, is just V. We show the connection between the structural matrixQ in the formal solution of a boundary value problem formulated for volume V and the so called auxiliary matrix of the graph Γ _v associated with V. We show boundary value problems to be isomorphic if the graphs associated with the volumes are isomorphic, or, if the covering groups are Sunada pairs.     

Local chain‐configuration dependence of the mechanisms of the chemical reaction of poly(vinyl chloride). IX. Novel results on stereoselectivity of chlorination reaction

A poly(vinyl chloride) (PVC) sample was chlorinated in solution in the presence of 2,2′‐azobisisobutyronitrile and by the fluid‐bed method. The aim was to evaluate the scope of the stereoselectivity of the chlorination reaction. The quantitative microstructural analysis of the residual PVC with a degree of chlorination was followed by ¹³C NMR spectroscopy. From the evolution of the content of isotactic (mm), heterotactic (mr), and syndiotactic (rr) triads and of mmmm, mmmr, and rmmr isotactic pentads in the unchlorinated parts of the polymer, it was unambiguously inferred that the chlorination reaction proceeds by a stereoselective mechanism in that the mr heterotactic triads are the most reactive structures followed by the isotactic triad at mmmr and rmmr pentads. This conclusion was confirmed on the basis of the Fourier transform infrared results. The results provide valuable information regarding the effect of tacticity and related local conformations in the chemical reactions of PVC. © 2003 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 41: 508–519, 2003     

Thermodynamic Limit and Proof of Condensation for Trapped Bosons

We study condensation of trapped bosons in the limit when the number of particles tends to infinity. For the noninteracting gas we prove that there is no phase transition in any dimension, but in any dimension, at any temperature the system is 100% condensated into the one-particle ground state. In the case of an interacting gas we show that for a family of suitably scaled pair interactions, the Gross–Pitaevskii scaling included, a less-than-100% condensation into a single-particle eigenstate, which may depend on the interaction strength, persists at all temperatures.     

On the Bol Loops

In the present paper, the Bol loops and related groups are studied. We suggest a universal way to construct a Bol loop and find criteria for simplicity and finiteness of such loops.     

The calculation of neutron self-shielding factors of a group of isolated resonances

The resonance neutron self-shielding factor, G _res, is required in neutron metrology and activation data analysis. In a previous paper, the authors have shown that a dimensionless variable can be introduced which converts the dependence of G _res on the physical and nuclear properties of the material samples into an universal curve, valid for the isolated resonances of any nuclide. This work presents a methodology based on the universal curve, which enables to calculate G _res for a group of isolated resonances by weighting its individual contributions. A good agreement was reached with results calculated by the MCNP code and with experimental values for Mo foils and wires. This revised version was published online in July 2006 with corrections to the Cover Date.