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61.
This paper considers a novel formulation of the multi-period network interdiction problem. In this model, delivery of the maximum flow as well as the act of interdiction happens over several periods, while the budget of resource for interdiction is limit. It is assumed that when an edge is interdicted in a period, the evader considers a rate of risk of detection at consequent periods. Application of the generalized Benders decomposition algorithm considers solving the resulting mixed-integer nonlinear programming problem. Computational experiences denote reasonable consistency with expectations.  相似文献   
62.
A novel N‐doped MoO 3 @SiC hollow nanosphere has been synthesized through two steps. Due to the first step, N‐doped MoO2@C nanosphere was synthesized using the hydrothermal method and in the second step, Si‐C bonds were formed through the low‐temperature magnesiothermic method and MoO 3 @SiC hollow nanosphere was produced. The prepared nanostructures were identified by various techniques such as IR, XRD, XPS, BET/BJH, SEM/EDS, and Raman spectroscopy. Results show that converting of C to SiC increase the surface area from 17 to 241 m2/g with remarkably decrease in pore diameter. Also, molybdenum is present in the form of MoO2 in carbon catalyst while during magnesiothermic process, it transfers to MoO3 form in the SiC catalyst. The synthesized products were employed as catalysts in oxidative desulfurization of model fuel. The results displayed that MoO 3 @SiC hollow nanostructure shows a superior catalytic activity (99.9%, 40 min) compared to C support (56%, 60 min). Furthermore, the recycling of MoO2@C catalyst shows a dramatic decrease even after the first run, while, SiC support exhibit higher stability during the stronger interaction between molybdenum catalyst and SiC support.  相似文献   
63.
Preparation, characterization, and catalytic properties of bimetallic coordination polymer constructed from 2‐aminoterephthalic acid as linker, zinc cations as node, and cis‐dioxo molybdenum units as catalytic active sites are reported via two pathways. Molybdenum centers were placed in N,O positions created by condensation reaction of 2‐aminoterephthalic acid with salicylaldehyde while zinc cations coordinated via carboxylic acid groups of linker to achieve infinite chains of metalo‐ligand. The obtained coordination polymer was fully characterized and its catalytic properties in the epoxidation of olefins with tert‐butyl hydroperoxide (TBHP) described. In comparison with previously reported heterogenized molybdenum catalysts, this new coordination polymer exhibited good conversion as well as high selectivity in the epoxidation of olefins. The catalyst is stable under ambient conditions and could be reused as active catalyst for at least five times.  相似文献   
64.
This work describes the synthesis of novel 1,2,3‐triazole‐4‐linked (2E,6E)‐2‐benzylidene‐6‐(4‐nitrobenzylidene)cyclo‐hexanones starting from cyclohexanone. 1‐(Cyclohex‐1‐en‐1‐yl)piperidine, the enamine from cyclohexanone and piperidine, reacted with 4‐nitrobenzaldehyde to obtain 2‐(4‐nitrobenzylidene)cyclohexanone. Condensation of the latter compound with (prop‐2‐yn‐1‐yloxy)benzaldehyde derivatives under acidic conditions gave (4‐nitrobenzylidene)‐[(prop‐2‐yn‐1‐yloxy)‐benzylidene]cyclohexanones. Finally, ‘click reaction’ of these derivatives and various organic azides led to the title compounds. All compounds were examined by MTT assay for cytotoxic activity in one human breast cancer cell line, MDA‐MB‐231.  相似文献   
65.
66.
The surface of a LDPE was modified by Ar, O2, N2, CO2 gaseous plasma. The changes in surface morphology and surface wettability were investigated using AFM and SEM. The surface chemical changes of LDPE were also characterized by FTIR-ATR. The SEM and AFM results demonstrated variable changes in surface roughness for different types of plasma gas used, the changes being more for the Ar and N2 plasma treatments. Considering the nature of the LDPE film, XRD studies were carried out to determine changes in the percentage crystalinity. The results showed that all low pressure O2, Ar, N2, CO2 gas plasmas improved the wettability of LDPE films. Contact angles decreased significantly depending on the discharge powers and exposure times. Surface morphology was also found to vary with plasma discharge powers, exposure times, and the type of gas being used. Ar and N2 gas plasmas in general produced more superior results.  相似文献   
67.
A wide range of aliphatic or aromatic sulfides are selectively oxidized to the corresponding sulfoxides using ammonium cerium (IV) nitrate (CAN) and a catalytic amount of KBr or NaBr in the presence of wet SiO2 in CH2Cl2 under heterogeneous conditions in moderate to high yields.  相似文献   
68.
Isoquinoline reacts with ethyl bromopyruvate in the presence of dialkyl acetylenedicarboxylates or diaryloylacetylenes to produce dialkyl 1-(2-ethoxy-2-oxoacetyl)pyrrolo[2,1-a]isoquinoline-2,3-dicarboxylates or ethyl 2-[2,3-diaryloylpyrrolo[2,1-a]isoquinoline-1-yl]-2-oxoacetates in good yields.  相似文献   
69.
A very mild and highly efficient synthesis of some novel 1H‐1,2,3‐triazolyl carboacyclic nucleosides via a ‘Click’ Huisgen cycloaddition of N‐propargyl nucleobases and azido alcohols using Cu/aminoclay/reduced graphene oxide nanohybrid (Cu/AC/r‐GO nanohybrid) as nanocatalyst is described. The preparation and characterization of Cu/AC/r‐GO nanohybrid are discussed. This catalyst was characterized by X‐ray diffraction, FT‐IR, TEM, and energy‐dispersive analysis of X‐ray techniques. Cu/AC/r‐GO nanohybrid is a stable and highly efficient heterogeneous nanocatalyst that can be easily prepared, used, and restored from the reaction mixture by simple filtration, and reused for many consecutive trials without significant decrease in activity.  相似文献   
70.
First, the extraction and preconcentration of ultratrace amounts of lead(II) ions was performed using microliter volumes of a task‐specific ionic liquid. The remarkable properties of ionic liquids were added to the advantages of microextraction procedure. The ionic liquid used was trioctylmethylammonium thiosalicylate, which formed a lead thiolate complex due to the chelating effect of the ortho‐positioned carboxylate relative to thiol functionality. So, trioctylmethylammonium thiosalicylate played the roles of both chelating agent and extraction solvent simultaneously. Hence, there is no need to use a ligand. The main parameters affecting the efficiency of the method were investigated and optimized. Under optimized conditions, this approach showed a linear range of 2.0–24.0 ng/mL with a detection limit of 0.0010 ng/mL. The proposed method was applied to the extraction and preconcentration of lead from red lipstick and pine leaves samples prior to electrothermal atomic absorption spectroscopic determination.  相似文献   
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