竞争型“以旧换再”闭环供应链策略选择及生产决策研究

针对两阶段闭环供应链系统,研究了古诺竞争型闭环供应链中的“以旧换再”策略选择问题。研究发现:(1)企业如何及何时实施“以旧换再”策略取决于自身及竞争企业的再制造水平。再制造水平不仅影响了企业的“以旧换再”数量,同时还会影响产品市场份额及利润。(2)“以旧换再”策略可以提高企业竞争力,增加企业产品市场份额和提高收益;(3)提高 “以旧换再”补贴及再制造产品接受度, 降低“二手市场”价格,均可以降低企业实施“以旧换再”策略和提高企业的“以旧换再”数量。     

Palladium Release in Electrothermal Atomic Absorption Spectrometry

The absorbance signal in electrothermal atomic absorption spectrometry is a result of the processes of atom formation and dissipation and first of all depends on the initial generation of atoms from the surface. The rising part of the absorbance time profiles can be used for characterization of the release of the metals like Pd, Ag, Au etc. The method is applied to investigate the palladium release from a pyrocoated graphite support at different initial masses of the Pd. The kinetic parameters are evaluated and conclusions about the distribution of palladium on the graphite surface are made. The estimated values of apparent activation energies depend on the initial mass of analyte. The advantages and limitations of the present approach are discussed.     

Quinoline-Based “On-Off” Fluorescent Sensor for Acetate: Effect of Link Mode between Binding Sites and Fluorophore on Fluorescence Changes

ABSTRACT

A novel colorimetric and fluorescence anion sensor based on 8-nitroquinolyl-2-aldehyde phenyl-thiosemicarbazone (1) was designed and synthesized according to the approach that the binding sites were covalently linked to the signaling units. In DMSO, sensor 1 exhibited a naked-eye color change from colorless to yellow upon complexation with acetate. The association constant of 1 for acetate ion was determined to be 1.20 × 10³ M^?1 by nonlinear fitting analyses of the titration curves. The strong interactions of compound 1 with acetate ion could be rationalized on basis of not only the guest basicity but also shape complementarity between 1 and acetate. In addition, the fluorescence emission of 1 was effectively quenched upon addition of acetate ions owing to the fact that the photoinduced electron transfer (PET) was enhanced.     

Reaction of N-acylthioureas with electrophilic reagents : Synthesis of 1,3,5-oxadiazinium salts, 1,3,5-thiadiazinium salts, 1,2,4-dithiazolium salts and benzothiazoles

N-Acylthioureas 1 can be easily transformed into 2,4-diamino-6-aryl-1,3,5-oxadiazinium salts 12, 2,4-diamino-6-aryl-1,3,5-thiadiazinium salts 13,3-amino-5-aryl-1,2,4-dithiazolium salts 19 and 2-acylimino-benzothiazolines 22, respectively by reaction with different electrophiles. The structure of the compounds prepared is confirmed by analytical data as well as by chemical transformations.     

Existence of infinitely many stationary solutions of the L2-subcritical and critical NLSE on compact metric graphs

We investigate the existence of stationary solutions for the nonlinear Schrödinger equation on compact metric graphs. In the $L^2$-subcritical setting, we prove the existence of an infinite number of such solutions, for every value of the mass. In the critical regime, the existence of infinitely many solutions is established if the mass is lower than a threshold value, while global minimizers of the NLS energy exist if and only if the mass is lower or equal to the threshold. Moreover, the relation between this threshold and the topology of the graph is characterized. The investigation is based on variational techniques and some new versions of Gagliardo–Nirenberg inequalities.     

“互联网+回收”情境下基于演化博弈的电子废弃物回收合作机理研究

基于“互联网+回收”情境,研究网络回收商和流动回收小贩在电子废弃物回收中的竞合关系,构建演化博弈模型,刻画演化博弈过程,分析相关因素对演化稳定策略走向的影响。研究结果表明,网络回收商和流动回收商小贩选择合作策略的概率与违约惩罚力度、合作后的超额收益正相关,与合作后的共同成本、单独选择合作策略付出的成本以及因搭便车行为增加的收益负相关。由于分别存在最优的超额收益分配率和共同成本分摊率,网络回收商和流动回收小贩选择合作策略的概率最大。     

New Route to Polymeric Nanoparticles by Click Chemistry Using Bifunctional Cross-Linkers

A new route to functional polymeric nanoparticles (PNPs) of different chemical nature in the 3 to 20 nm size range is reported by combining both radical addition fragmentation chain transfer (RAFT) polymerization and “click” chemistry (CC) techniques. RAFT polymerization was employed for the synthesis of well-defined statistical copolymers with pending –Cl groups along the macromolecular chain. After transformation of the –Cl groups to –N₃ groups by treatment with sodium azide, an appropriate bifunctional cross-linker is employed to obtain PNPs under CC conditions promoting intramolecular cycloaddition (cross-linking). Following this new route, polystyrene, poly(alkyl (meth)acrylate), polymethacrylic acid, poly(sodium styrenesulfonate) and poly(N-isopropyl) NPs have been synthesized and in-deep characterized.     

Dealing with external actions in belief causal networks

Graphical models are efficient and simple ways to represent dependencies between variables. We introduce in this paper the so-called belief causal networks where dependencies are uncertain causal links and where the uncertainty is represented by belief masses. Through these networks, we propose to represent the results of passively observing the spontaneous behavior of the system and also evaluate the effects of external actions. Interventions are very useful for representing causal relations, we propose to compute their effects using a generalization of the “do” operator. Even if the belief chain rule is different from the Bayesian chain rule, we show that the joint distributions of the altered structures to graphically describe interventions are equivalent. This paper also addresses new issues that are arisen when handling interventions: we argue that in real world applications, external manipulations may be imprecise and show that they have a natural encoding under the belief function framework.     

Synthesis of a series of ethylene glycol modified water-soluble tetrameric TPE-amphiphiles with pyridinium polar heads: Towards applications as light-up bioprobes in protein and DNA assay,and wash-free imaging of bacteria

Available online Development of water soluble AIE-active “light-up” bioprobes for the detection of biomacromolecules has drawn huge research interests in recent past. In this study, a series of ethylene glycol modified water soluble tetrameric tetraphenylethylene amphiphiles with pyridinium polar heads (TPE-xEG-Py, x = 3, 4, 6 or 1a-c) have been synthesized by varying the ethylene glycol spacer. Their unique structure allows them to form vesicles and other nanoaggregates in aqueous solutions. These amphiphiles were successfully utilized for fluorimetric detection and quantitation of BSA and DNA based on the electrostatic interactions to trigger AIE-emission from the TPE moiety. The electrostatic interaction was also proved very effective in wash-free imaging of both Gram-negative (E. coli) and Gram-positive (S. aureus) bacteria with up to 92 folds increase in fluorescence response within bacterial concentration 0–12 × 10⁸ CFU mL^?1. The strategy is advantageous due to cost-effective and easy synthesis, high water solubility, and fast response.