Fusion around the barrier for 7Li+12C

Fusion cross-sections for the ⁷Li + ¹²C reaction have been measured at energies above the Coulomb barrier by the direct detection of evaporation residues. The heavy evaporation residues with energies below 3 MeV could not be separated out from the α-particles in the spectrum and hence their contribution was estimated using statistical model calculations. The present work indicates that suppression of fusion cross-sections due to the breakup of ⁷Li may not be significant for ⁷Li + ¹²C reaction at energies around the barrier.     

Explicit portfolio for unit-linked life insurance contracts with surrender option

Introducing a surrender option in unit-linked life insurance contracts leads to a dependence between the surrender time and the financial market. [J. Barbarin, Risk minimizing strategies for life insurance contracts with surrender option, Tech. rep., University of Louvain-La-Neuve, 2007] used a lot of concepts from credit risk to describe the surrender time in order to hedge such types of contracts. The basic assumption made by Barbarin is that the surrender time is not a stopping time with respect to the financial market.The goal of this article is to make the hedging strategies more explicit by introducing concrete processes for the risky asset and by restricting the hazard process to an absolutely continuous process.First, we assume that the risky asset follows a geometric Brownian motion. This extends the theory of [T. Møller, Risk-minimizing hedging strategies for insurance payment processes, Finance and Stochastics 5 (2001) 419–446], in that the random times of payment are not independent of the financial market. Second, the risky asset follows a Lévy process.For both cases, we assume the payment process contains a continuous payment stream until surrender or maturity and a payment at surrender or at maturity, whichever comes first.     

Mechanism of copper underpotential deposition at Pt(<Emphasis Type="Italic">hkl</Emphasis>)-electrodes: Quantum-chemical modelling

Mechanism of copper underpotential deposition at stepped faces of platinum single crystals Pt(hkl) is studied using cyclic voltammetry, scanning probe microscopy, and quantum-chemical modelling. It is shown that the first stage of UPD is one-dimensional decoration of the (100)- or (110)-orientated steps, then copper monolayer forms at (111)-terraces. The final stage is the secondary step decoration. Quantum-chemical modelling, with the using of long-distance potentials of the Cu-Pt and Cu-Cu pair interactions, allows estimating the energy of copper adsorption at different structure elements of the substrate (steps, kinks, terraces) and revealing the succession of the adatom monolayer formation; it also provides additional information for the identifying of the nature of voltametric peaks for different stages of the copper adsorption-desorption.     

Buffer sizing in multi-product multi-reactor batch processes: Impact of allocation and campaign sizing policies

This paper studies the impact of management policies, such as product allocation and campaign sizing, on the required size of the finished goods inventories in a multi-product multi-reactor batch process. Demand, setup and batch processing times for these products are assumed to be stochastic, and the inventory buffer for every product type needs to be such that target customer service levels are met. To perform this analysis, we develop a queueing model that allows us to explicitly estimate service levels as a function of the buffer size, and the allocation/campaign sizing policies. This model can be used to evaluate the service level given an existing buffer configuration, as well as to determine the buffer sizes required across products to meet a pre-specified service level. It also allows us to formulate a number of insights into how product allocation decisions and campaign planning policies affect buffer sizing decisions in symmetric production systems.     

Determination of trace amounts of nickel by atomic-absorption spectrometry after carbonyl generation

A sensitive and reliable method for the atomic-absorption spectrometric determination of micro-amounts of Ni in organic and inorganic samples has been developed, with separation of nickel by carbonyl generation. Foreign anions and cations do not interfere. Only metallic iron hampers the generation of Ni(CO)(4) but this interference can be avoided if the latter is formed in nitric acid medium. In the range 0.02-0.1 mug, Ni can be determined with a precision of about 10%. The detection limit of the proposed method is 10 ng in the aliquot used.