供应中断下最优分配和应急采购策略的比较

最优分配采购策略和应急采购策略被广泛应用于供应中断风险管理中,基于最优分配采购策略和应急采购策略,研究了由两个制造商与两个零售商组成的两级供应链在供应中断下的订购和生产决策问题,给出了最优订购和最优生产策略.通过数值例子就可靠性如何影响制造商的最优价格和利润进行了比较.结果表明:随着可靠性的增加,两个制造商的最优价格呈递减态势,且制造商A的递减幅度小于制造商B的递减幅度;当可靠性低于0.3时,制造商A的最优价格低于制造商B的最优价格,当可靠性高于0.3时,制造商A的最优价格高于制造商B的最优价格.随着可靠性的增加,制造商A的利润呈递减态势,制造商B的利润呈递增态势;当可靠性低于0.8时,制造商A的利润高于制造商B的利润,当可靠性低高于0.8时,制造商A利润低于制造商B的利润.     

Xe~(53+)离子与Xe原子碰撞过程中的辐射电子俘获和辐射退激发光谱的理论研究

基于多组态Dirac-Fock方法和密度矩阵理论,系统地研究了在197 Me V/u的碰撞能量下,Xe~(53+)离子与Xe原子的辐射电子俘获过程(REC)以及电子被俘获到激发态后辐射退激发产生的特征谱线.计算了炮弹Xe~(53+)离子俘获电子到不同壳层np_(1/2,3/2)(n=2—5)的总截面与相应的REC光子能量和角分布,以及由激发组态1snp_(1/2,3/2)(n=2—5)J_f=1向基态1s~2Jd=0辐射退激发的跃迁能量、跃迁概率和特征光子的角分布和线性极化度.计算结果表明,辐射光子具有显著的角各向异性特征.此外,1snp_(3/2)J_f=1→1s~2J_d=0退激发特征光子也显示出很强的线性极化和角各向异性特征,而1snp_(1/2)J_f=1→1s~2J_d=0退激发特征光子的线性极化度趋于零并且角分布也趋于各向同性.     

The Organosilicon thin Film Deposited Using an Atmospheric Pressure Dual‐Frequency 50 kHz/33 MHz Frequency MicroPlasma Jet

In this paper, an atmospheric pressure dual‐frequency (50 kHz/33 MHz) micro‐plasma jet was used to deposit organosilicon film. The discharge generated in atmospheric environment. Plasma composition was characterized by optical emission spectroscopy. With introduction of tetraethyl orthosilicate, we observed various spectra, for example Si(251.6 nm), OH(308.9 nm), C(247.8 nm), O(777.5 nm). Abundant reactive radical species which are benefit to film deposition were generated in plasma. The deposited film was characterized by scanning electron microscopy, X‐ray photoelectron spectroscopy and Fourier transform infrared spectroscopy. The film is mostly composed of Si and O. The film has Si‐O‐Si backbone with a small number of organic component (‐CHx). (© 2016 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Determination of isoniazid among pharmaceutical samples and the patients’ saliva samples by using potassium ferricyanide as spectroscopic probe reagent

A novel method to determine isoniazid with high sensitivity and good selectivity has been established by using potassium ferricyanide as spectroscopic probe reagent. In the presence of potassium ferricyanide, it has been demonstrated that iron(III) is reduced to iron(II) by isoniazid at pH 4.0. In addition, the in situ formed iron(II) reacts with potassium ferricyanide to give soluble prussian blue. The absorbance of soluble prussian blue is measured at the absorption maximum of 735 nm, and the amount of isoniazid can be calculated based on this absorbance. A good linear relationship of the concentration of isoniazid versus absorbance is observed with a linear range of 0.040-8.00 μg mL⁻¹. The linear regression equation is A = −0.00286 + 0.28588C (μg mL⁻¹) with a correlation coefficient of 0.9992. The detection limit (3σ/k) is 0.037 μg mL⁻¹, and its relative standard deviation (R.S.D.) is 0.35% (n = 11). Moreover, the apparent molar absorption coefficient of indirect determination of isoniazid is 3.92 × 10⁴ L mol⁻¹ cm⁻¹. The parameters with regard to determination are optimized, and the reaction mechanism is discussed. This method has been successfully applied to the determination of isoniazid in pharmaceutical samples and saliva samples of patients.     

Synthesis, characterization and properties of biodegradable polylactic acid-β-cyclodextrin cross-linked copolymer microgels

The novel biodegradable polylactic acid-β-cyclodextrin (PLA-β-CD) cross-linked copolymer microgels were prepared by the radical copolymerization of PLA macromonomer and polymerizable β-CD derivatives. The β-CD derivatives with various numbers of polymerizable vinyl groups were synthesized from 1-allyloxy-2,3-epoxy propane (also called allylglycidyl ether, AGE) and β-CD. The chemical structures of polymerizable monomers were determined by NMR. The thermal properties, size, morphology, in vitro degradation and swelling behavior of the microgels were investigated. The results indicated that the microgels were stable under thermal conditions up to 200 °C. The microgels were spherical in aqueous solution. The hydrophilicity of the microgels increased with increasing β-CD contents, while the swelling ratios and degradation rate decreased. The more vinyl groups on β-CD, the higher cross-linked density, which resulted in a decrease of the swelling ratios and the rate of degradation.     

Microwave induced efficient synthesis of (un)substituted benzaldehyde (5‐aryl‐1,3,4‐thiadiazol‐2‐yl)hydrazones using silica‐supported dichlorophosphate as a recoverable dehydrant

(Un)substituted benzaldehyde (5‐aryl‐1,3,4‐thiadiazol‐2‐yl)hydrazones were efficiently synthesized by reactions of (un)substituted benzaldehyde thiocarbohydrazones with aromatic carboxylic acids by using silica‐supported dichlorophosphate as a recoverable dehydrant under microwave irradiation. The protocol has advantages of short reaction time, high yield, easy work‐up procedure and no environmental pollution.     

Visible light photochemical synthesis of ultrasmall palladium/copper bimetallic particles at room temperature and its catalytic application in degradation of p-NP

Pt-based metals are very effective catalysts widely adopted in many fields. But the high cost prevents its further industrial application. One of the effective ways to solve the problem is to replace platinum with relatively cheap palladium and its alloy with copper. However, producing Pd/Cu bimetallic catalysts efficiently and economically with controllable particle size and uniform distribution is still challenging, especially when trying to reduce the consumption of precious metals. In this paper, ultrasmall palladium/copper (Pd/Cu) bimetallic catalysts with even dispersion were prepared on multi-walled carbon nanotubes (MWCNTs) by adding polyethylene glycol 400 (PEG 400) as a reducing agent and stabilizer under visible light irradiation at room temperature. The catalytic performance was studied in the catalysis of p-nitrophenol (p-NP) reduction. Of all the bimetallic catalysts produced in different conditions, the best one was obtained under the reaction condition of pH = 7 and violet light irradiation (wavelength 380–435 nm). The average particle size of 0.85 nm, and the apparent rate constant in the catalysis is 1.47 min^?1. This research probes the role of visible light as a key kinetic controlling method in the formation of ultrasmall particles (UPs). It proves the effectiveness of using visible light irradiation as an effective and more “green chemistry” approach to get precious metal UPs as catalysts beyond the traditional ultraviolet or laser photochemistry methods.     

Insight into Crystal Structures,Hirshfeld Surfaces and Fluorescent Properties of Multinuclear Co(II) and Ni(II) Salamo-Based Complexes Involving Lone Pair π-Interactions

Russian Journal of General Chemistry - Two multi-nuclear Co(II) and Ni(II) complexes, [{Co3(L)2(EtOH)2(μ-OAc)2}2]·2CH3CH2OH· CH2Cl2·CHCl3·CH3CN (1) and...     

Sorptive extraction of pesticides from food and environmental samples using metal organic framework-based adsorbents

Sorptive pre-concentration of pesticide residues in food and environmental samples is increasingly gaining momentum. This can be attributed to fact that most sorptive extraction techniques are solvent-free as well as the availability of emerging sorbents with relatively high adsorption capacities. Metal organic frameworks (MOFs) are among the emerging sorbents that have captured the interests of many researchers during pesticide analysis. There are many types of MOFs that have been used by researchers to pre-concentrate pesticides in food and environmental samples. Some researchers have successfully used MIL-based MOFs during sorptive extraction of pesticides in complex matrices. This review gives a detailed discussion of their application during pesticide pre-concentration. Other researchers have used the ZIF series of MOFs for the sorptive pre-concentration of pesticides in food and environmental samples. The utilisation of the ZIF series of MOFs during pesticide pre-concentration is well-articulated in this review. The review also devoted to the application of UiO and HKUST series of MOFs during the pre-concentration of pesticides in food and environmental samples. In addition, the challenges associated with the use of MOFs during sorptive pre-concentration of pesticides are also discussed in this review.