The scheduling of deliveries in a production-distribution system with multiple buyers

In a real production and distribution business environment with one supplier and multiple heterogeneous buyers, the differences in buyers’ ordering cycles have influence on production arrangements. Consequently, the average inventory level (AIL) at the supplier’s end is affected by both the production policy and the ordering policy, typically by the scheduling of deliveries. Consequently, the average inventory holding cost is most deeply affected. In this paper, it is proposed that the scheduling of deliveries be formulated as a decision problem to determine the time point at which deliveries are made to buyers in order to minimize the supplier’s average inventory. A formulation of the average inventory level (AIL) in a production cycle at the supplier’s end using a lot-for-lot policy is developed. Under the lot-for-lot policy, the scheduling of deliveries (SP) is formulated as a nonlinear programming model used to determine the first delivery point for each buyer with an objective to minimize the sum of the product of the individual demand quantity and the first delivery time for each buyer. Thus, the SP model determines not only the sequence of the first deliveries to individual buyers, but also the time when the deliveries are made. An iterative heuristic procedure (IHP) is developed to solve the SP model assuming a given sequence of buyers. Six sequence rules are considered and evaluated via simulation.     

Enhanced targeted energy transfer for adaptive vibration suppression of pipes conveying fluid

Nonlinear Dynamics - In this paper, a nonlinear energy sink and a negative stiffness element are integrated for achieving enhanced, passive, and adaptive vibration suppression for a pipe conveying...     

Bioinspired polymer functionalized with a diiron carbonyl model complex and its assembly onto the surface of a gold electrode via “click” chemistry

A complex pendant with two ethynyl groups, [Fe₂(μ‐SCH₂CCH)₂(CO)₆] ( 2 ), as a model of the diiron subunit of [FeFe]‐hydrogenase was polymerized and the {Fe₂(CO)₆} core was successfully incorporated into the polymer matrix. The polymer was characterized by a variety of spectroscopic techniques, TGA, FTIR, SEM, TEM, and NMR. The resultant polymer was immobilized via “click” chemistry using its terminal C?CH bond onto the surface of a gold electrode, which was premodified with azidothiol by self‐assembled monolayer (SAM). The assembled electrode showed electrochemical responses. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 2410–2417, 2010     

Poly(N‐vinylcarbazole) chemically modified graphene oxide

A new soluble donor‐acceptor type poly(N‐vinylcarbazole)‐covalently functionalized graphene oxide (GO‐PVK) has been synthesized by reaction of DDAT (S‐1‐dodecyl‐S′‐(α,α′‐dimethyl‐α″‐aceticacid)trithiocarbonate)‐PVK with GO‐toluene‐2,4‐diisocynate. The incorporation of sufficient amount of PVK chains makes the modified GO nanosheets readily dispersible in organic solvents. The resulting material exhibits an enhanced solubility of 10 mg/mL in organic solvents. Covalent grafting of PVK onto the edge and surface of GO nanosheets did not change the carbazole absorption in the ultraviolet region, but substantially reduced the absorption intensity of GO in the visible region. The intensity of the emission band of GO‐PVK at 437 nm was a little bit quenched when compared with that of DDAT‐PVK, suggesting intramolecular quenching from PVK to GO. Such intramolecular quenching process may involve energy or electron transfer between the excited singlet states of the PVK moiety and the GO moiety. The HOMO/LUMO values and the energy bandgap of GO‐PVK experimentally estimated by the onset of the redox potentials are ?5.60, ?3.58, and 2.02 eV, respectively. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 2642–2649, 2010     

A study on stress intensity factors and singular stress fields of three-dimensional interface crack

By using the finite-part integral concepts and limit technique, the hypersingular integrodifferential equations of three-dimensional (3D) planar interface crack were obtained; then the dominant-part analysis of 2D hypersingular integral was further used to investigate the stress fields near the crack front theoretically, and the accurate formulae were obtained for the singular stress fields and the complex stress intensity factors. After that, a numerical method is proposed to solve the hypersingular integrodifferential equations of 3D planar interface crack, and the problem of elliptical planar crack is then considered to show the application of the method. The numerical results obtained are satisfactory. Project supported by the Foundation of Solid Mechanics Open Research Laboratory of State Education Commission at Tongji University and the National Natural Science Foundation.     

β—环糊精／环氧氯丙烷交联聚合物毛细管气相色谱固定相的制备？…

参考文献合成了一种非水溶性β－环糊精／环氧氯丙烷交联聚合物，采用不同的方法将其涂渍到弹性石英毛细管柱上，考察了毛细管柱的基本性能，对某些芳香位置异构体和对映体进行了色谱分离。     

Synthesis,structure and biological activity of diorganotin derivatives with pyridyl functionalized bis(pyrazol‐1‐yl)methanes

Three pyridyl functionalized bis(pyrazol‐1‐yl)methanes, namely 2‐[(4‐pyridyl)methoxyphenyl] bis(pyrazol‐1‐yl)methane (L¹), 2‐[(4‐pyridyl)methoxyphenyl]bis(3,5‐dimethylpyrazol‐1‐yl)methane (L²) and 2‐[(3‐pyridyl)methoxyphenyl]bis(pyrazol‐1‐yl)methane (L³) have been synthesized by the reactions of (2‐hydroxyphenyl)bis(pyrazol‐1‐yl)methanes with chloromethylpyridine. Treatment of these three ligands with R₂SnCl₂ (R = Et, n‐Bu or Ph) yields a series of symmetric 2:1 adducts of (L)₂SnR₂Cl₂ (L = L¹, L² or L³), which have been confirmed by elemental analysis and NMR spectroscopy. The crystal structures of (L²)₂Sn(n‐Bu)₂Cl₂·0.5C₆H₁₄ and (L³)₂SnEt₂Cl₂ determined by X‐ray crystallography show that the functionalized bis(pyrazol‐1‐yl)methane acts as a monodentate ligand through the pyridyl nitrogen atom, and the pyrazolyl nitrogen atoms do not coordinate to the tin atom. The cytotoxic activity of these complexes for Hela cells in vitro was tested. Copyright © 2010 John Wiley & Sons, Ltd.     

Theoretical investigation into optical and electronic properties of oligothiophene derivatives with phenyl ring as core or end-capped group in linear and V-shape

A series of thiophene-based oligomers has been designed to explore their optical, electronic, and charge transport properties for charge transport materials. These oligomers consist of oligothiophene, oligo(thienylenevinylene), and m- or p-phenyl as the core in two shapes (linear shape and V-shape). Phenyl ring as the end-capped group is also investigated in the linear shape. The DFT-PBE0/6-31G(d,p) and the TD-PBE0/6-31+G(d,p) calculated results reported herein show that the V-shape oligomers have larger HOMO-LUMO gaps because of meta-substitutions on phenyl cores, corresponding to blue shifts of absorption spectra. The linear oligomers with phenyl ring as end-capped group display red shifts of absorption spectra. The V-shape oligomers provide small reorganization energies. Our recommended polymer possessing 1,2,4-phenyl core and longer OTV side fragments is a good candidate for the design of charge transport and/or solar cell materials.     

Synthesis of a water-soluble cationic chiral diamine ligand bearing a diguanidinium and application in asymmetric transfer hydrogenation

A novel water-soluble cationic N-monosulfonated chiral diamine ligand diguanidinium 1c was easily prepared from (R,R)-DPEN and its rhodium complex and was successfully applied in the asymmetric transfer hydrogenation of prochiral ketones and imines in water by using sodium formate and formic acid as co-hydrogen donors. Various substrates were reduced with high yields and good to excellent enantioselectivities (up to >99% ee).