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1.
An optimization approach for planning daily drayage operations 总被引:1,自引:0,他引:1
Yetkin Ileri Mokhtar Bazaraa Ted Gifford George Nemhauser Joel Sokol Erick Wikum 《Central European Journal of Operations Research》2006,14(2):141-156
Daily drayage operations involve moving loaded or empty equipment between customer locations and rail ramps. Our goal is to
minimize the cost of daily drayage operations in a region on a given day. Drayage orders are generally pickup and delivery
requests with time windows. The repositioning of empty equipment may also be required in order to facilitate loaded movements.
The drayage orders are satisfied by a heterogeneous fleet of drivers. Driver routes must satisfy various operational constraints.
We present an optimization methodology for finding cost-effective schedules for regional daily drayage operations. The core
of the formulation is a set partitioning model whose columns represent routes. Routes are added to the formulation by column
generation. We present numerical results for real-world data which demonstrate that our methodology produces low cost solutions
in a reasonably short time. 相似文献
2.
Mert Mehmet Selçuk Mert Hatice Hande Sert Merve 《Journal of Thermal Analysis and Calorimetry》2019,136(4):1551-1561
Journal of Thermal Analysis and Calorimetry - Thermal energy storage systems provide efficiency in order to have better utilization of energy sources while protecting the environment. Thermal... 相似文献
3.
We report the first preparation of furo- and thieno-fused 1,3-diazepine-4,6-dione derivatives starting from ethyl 2-(2-methoxy-2-oxoethyl)-3-furancarboxylate and -thiophencarboxylate. The ester functionalities connected to the hetero-ring were converted regiospecifically into the desired amides. The ester groups attached to the methylene unit were converted into isocyanates via Curtius rearrangement. The ring-closure reaction was performed in the presence of lithium bis(trimethylsilyl)amide at room temperature to give furo- and thieno-fused diazepinone derivatives. 相似文献
4.
Merve lkhan 《Mathematical Methods in the Applied Sciences》2019,42(16):5143-5153
Norm of an operator T:X→Y is the best possible value of U satisfying the inequality and lower bound for T is the value of L satisfying the inequality where ‖.‖X and ‖.‖Y are the norms on the spaces X and Y, respectively. The main goal of this paper is to compute norms and lower bounds for some matrix operators from the weighted sequence space ?p(w) into a new space called as Fibonacci weighted difference sequence space. For this purpose, we firstly introduce the Fibonacci difference matrix and the space consisting of sequences whose ‐transforms are in . 相似文献
5.
Mixed matrix materials, containing poly(dimethylsiloxane), phosphine oxide-based polyimide, and zeolite Y were prepared by means of blending hybridisation. The thermal stability of the materials and the hydrophobic properties were enhanced. The decrease in the glass transition temperature of the materials with the increase in poly(dimethylsiloxane) content supported the polymer-chain flexibility. The pristine polyimide and the zeolite-filled polyimide exhibited the highest transparency. Fourier transform infrared (FTIR) spectroscopy confirmed that the increase in the amount of the lowest molecular mass poly(dimethylsiloxane) ingredient indicated strong alkyl and Si-O-Si stretching modes, whilst the alkyl and Si-O-Si stretching intensity decreased in the presence of the highest amount of and the highest molecular mass poly(dimethylsiloxane). The hydrophobic poly(dimethylsiloxane) moiety created an inverse relationship between the porosity of the materials (surface roughness) and the hydrophilicity. The nanocrystallite domain, identified by X-ray diffraction analysis (XRD) and possessing an exotherm crystallisation peak, occurred in the lowest amount of poly(dimethylsiloxane) with the highest molecular mass-based hybrid material. The nanocrystallite enhanced the storage modulus as determined by the dynamic mechanical analyser (DMA). The nanocrystalline formation resulted in a slight increase in the alkyl stretching and the Si-O-Si stretching of the lowest amount of and the highest molecular mass poly(dimethylsiloxane)-containing material over those of the lowest molecular mass poly(dimethylsiloxane) in the same amounts of material involved. 相似文献
6.
7.
We report herein the synthesis of a novel class of compounds, ethyl 4-oxo-4H-furo[3,2-c]pyran-6-yl carbonate, (7E)-7-[(dimethylamino)methylene]-4H-furo[3,2-c]pyran-4,6(7H)-dione, 5-oxo-N-phenyl-2,5-dihydro-4H-furo[3,2-b]pyrrole-4-carboxamide, and 5-oxo-N-phenyl-5,6-dihydro-4H-thieno[3,2-b]pyrrole-4-carboxamide starting from the corresponding acid derivatives. Intramolecular cyclization in the presence of thionyl chloride formed the target fused ring systems. Additional transformation was seen in the cyclization of furan-fused heterocycle. A mechanism was proposed based on experimental and computational findings. 相似文献
8.
Merve Sendur Abidin Balan Derya Baran Levent Toppare 《Journal of polymer science. Part A, Polymer chemistry》2011,49(18):4065-4070
Tuning the bandgap of electrochromic polymers is one of the important research topics in electrochromism. To understand clearly the effect of donor unit in donor–acceptor–donor‐type polymers, 2,3‐bis(4‐tert‐butylphenyl)‐5,8‐di(thiophen‐2‐yl)quinoxaline and 2,3‐bis(4‐tert‐butylphenyl)‐5‐(2,3‐dihydrothieno[3,4‐b][1,4]dioxin‐ 5‐yl)‐8‐(thiophen‐2‐yl)quinoxaline were synthesized and polymerized potentiodynamically. Their electrochemical and spectroelectrochemical studies were performed, and the results were compared with those of poly(2,3‐bis(4‐tert‐butylphenyl)‐5,8‐bis(2,3‐dihydrothieno[3,4‐b][1,4]dioxin‐5‐yl)quinoxaline) (Gunbas et al., Adv Mater 2008, 20, 691–695). A blue shift in the polymer π–π* transitions revealed that the bandgap of such polymers with the same acceptor unit is related to the electron density of donor units. © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011 相似文献
9.
Samed Atak Merve İçli‐Özkut Ahmet M. Önal Atilla Cihaner 《Journal of polymer science. Part A, Polymer chemistry》2011,49(20):4398-4405
Optical and electrochemical properties of regiosymmetric and soluble alkylenedioxyselenophene‐based electrochromic polymers, namely poly(3,3‐dibutyl‐3,4‐dihydro‐2H‐selenopheno[3,4‐b][1,4]dioxephine) (PProDOS‐C4), poly(3,3‐dihexyl‐3,4‐dihydro‐2H‐selenopheno[3,4‐b][1,4]dioxephine) (PProDOS‐C6), and poly(3,3‐didecyl‐3,4‐dihydro‐2H‐selenopheno[3,4‐b][1,4]dioxephine) (PProDOS‐C10), are highlighted. It is noted that these unique polymers have low bandgaps (1.57–1.65 eV), and they are exceptionally stable under ambient atmospheric conditions. Polymer films retained 82–97% of their electroactivity after 5000 cycles. The percent transmittance of PProDOS‐Cn (n = 4, 6, 10) films found to be between 55 and 59%. Furthermore, these novel soluble PProDOS‐Cn polymers showed electrochromic behavior: a color change form pure blue to highly transparent state in a low switching time (1.0 s) during oxidation with high coloration efficiencies (328–864 cm2 C?1) when compared to their thiophene analogues. © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011 相似文献
10.
T. Gamze Ulusoy Ghobadi Amir Ghobadi Merve Demirtas Muhammed Buyuktemiz Kubra N. Ozvural Elif Akhuseyin Yildiz Prof. Emre Erdem Prof. H. Gul Yaglioglu Prof. Engin Durgun Prof. Yavuz Dede Prof. Ekmel Ozbay Prof. Ferdi Karadas 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(35):8966-8976
The replacement of traditional ruthenium-based photosensitizers with low-cost and abundant iron analogs is a key step for the advancement of scalable and sustainable dye-sensitized water splitting cells. In this proof-of-concept study, a pyridinium ligand coordinated pentacyanoferrate(II) chromophore is used to construct a cyanide-based CoFe extended bulk framework, in which the iron photosensitizer units are connected to cobalt water oxidation catalytic sites through cyanide linkers. The iron-sensitized photoanode exhibits exceptional stability for at least 5 h at pH 7 and features its photosensitizing ability with an incident photon-to-current conversion capacity up to 500 nm with nanosecond scale excited state lifetime. Ultrafast transient absorption and computational studies reveal that iron and cobalt sites mutually support each other for charge separation via short bridging cyanide groups and for injection to the semiconductor in our proof-of-concept photoelectrochemical device. The reorganization of the excited states due to the mixing of electronic states of metal-based orbitals subsequently tailor the electron transfer cascade during the photoelectrochemical process. This breakthrough in chromophore-catalyst assemblies will spark interest in dye-sensitization with robust bulk systems for photoconversion applications. 相似文献