17 research outputs found

    An automated composite table algorithm considering zero liquid discharge possibility in water regeneration–recycle network

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    In this study, a novel Automated Composite Table Algorithm (ACTA) is developed for targeting the water regeneration–recycle network of single contaminant problem. The ACTA is based on Pinch Analysis, but is automated by taking into consideration the possibility of zero liquid discharge (ZLD) for the water network. In the existing literature, the targeting procedure for ZLD network is based on the graphical tool of Limiting Composite Curve (LCC). However, identification of key parameters (i.e. freshwater, wastewater, regenerated water flowrates, along with pre-regeneration concentrations) is very tedious for highly integrated water network system. The magnification around the turning point of LCC is required to identify the correct pinch points and targeting procedure is done iteratively until the reliable network targets can be determined. These limitations are now overcome by the ACTA, which is an improved version of Composite Table Algorithm that is capable of identifying key parameters algebraically for a given post-regeneration concentration. The newly developed ACTA is capable of handling a wide range of problems including ZLD and non-ZLD network, for both fixed load and fixed flowrate problems

    Synthesis of triazolylmethyl-linked nucleoside analogs via combination of azidofuranoses with propargylated nucleobases and study on their cytotoxicity

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    KARAYILDIRIM, Tamer/0000-0001-7451-0810; HALAY, Erkan/0000-0002-0084-7709WOS: 000429350900009Copper(I)-catalyzed azide-alkyne 1,3-dipolar cycloaddition reactions (CuAAC) between azidofuranoses and propargyl-nucleobases were carried out in the presence of CuSO4 center dot 5H(2)O and sodium ascorbate as catalytic system to provide the corresponding 1,4-disubstituted-1,2,3-triazole-bridged nucleoside analogs in good yields. Twelve new sugar-based triazolylmethyl-linked nucleoside analogs were synthesized and screened for their cytotoxic activity against MDA-MB-231, Hep3B, PC-3, SH-SY5Y, and HCT-116 cancer cell lines and control cell line (L929). Most of the compounds were moderately effective against all the cancer cell lines assayed. Particularly, among the tested compounds, 1,2,3-triazole-linked 5-fluorouracil-mannofuranose hybrid was found to be the most potent cytotoxic agent against HCT-116, Hep3B, SH-SY5Y cells with IC50 values of 35.6, 71.1, and 75.6 mu M, respectively. None of the triazolylmethyl-linked nucleoside analogs exhibited cytotoxic effect against the control cells L929.TUBITAK-Research Council of Turkey [114Z757]; TUBITAK-BIDEBTurkiye Bilimsel ve Teknolojik Arastirma Kurumu (TUBITAK) [2211A]This work was supported by TUBITAK-Research Council of Turkey with the project number 114Z757. Author E. Halay also offers his profound thanks to TUBITAK-BIDEB 2211A for their bursary support
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