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Bioremediation is an effective strategy for cleaning up organic contaminants, such as polycyclic aromatic hydrocarbons (PAHs) and volatile organic compounds (VOCs). Advanced bioremediation implies that biotic agents are more efficient in degrading the contaminants completely. Bioremediation by microbial degradation is often employed and to make this process efficient, natural and cost-effective materials can serve as supportive matrices. Clay/modified clay minerals are effective adsorbents of PAHs/VOCs, and readily available substrate and habitat for microorganisms in the natural soil and sediment. However, the mechanism underpinning clay-mediated biodegradation of organic compounds is often unclear, and this requires critical investigation. This review describes the role of clay/modified clay minerals in hydrocarbon bioremediation through interaction with microbial agents in specific scenarios. The vision is on a faster, more efficient and cost-effective bioremediation technique using clay-based products. This review also proposes future research directions in the field of clay modulated microbial degradation of hydrocarbons.

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Reference:
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI

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Microchip electrophoresis is a versatile separation technique. Electrochemical detection is suitable to apply to microdevices due to its easy integration to the fabrication process and good sensitivity and selectivity. Here we describe the procedures to prepare Pt band electrodes deposited on glass to couple to polydimethylsiloxane (PDMS) microchips aiming the separation and detection of nitrite using an isolated potentiostat.

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Reference:
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI

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In homogeneous catalysis, the catalyst is in the same phase as the reactant. The number of collisions between reactants and catalyst is at a maximum.In a patent, 1119-97-7, name is MitMAB, introducing its new discovery. Safety of MitMAB

The viscosity B-coefficients of the Jones-Dole equation for several alkyltrimethylammonium bromides in water have been determined over the temperature range 15-45 deg C.The effect of temperature on the solute-solvent interaction is discussed.It was found that the plot of the temperature coefficient of B, dB/dT, vs. the alkyl chain length of the solute shows a break point at ca.C7-C8, attributable to the effective range of the hydrophilic hydration of the solute.The results indicate that the lower derivatives possess structure breaking ability, while the higher derivatives are structure-formers. Keywords: Viscosity of solutions / B-coefficient / Amphiphiles / Alkyltrimethylammonium bromides

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Reference:
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI

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Catalysts function by providing an alternate reaction mechanism that has a lower activation energy than would be found in the absence of the catalyst. In some cases, the catalyzed mechanism may include additional steps.In a article, 448-61-3, molcular formula is C23H17BF4O, introducing its new discovery. Safety of 2,4,6-Triphenylpyrylium tetrafluoroborate

A facile three step process, under mild conditions, for the synthesis of 2,4-diarylfurans with the same or different substituents on the two aryl rings, starting from benzaldehydes and acetophenones, employing Haller-Bauer type cleavage of 2-aroyl-3,5-diarylfurans is described.

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Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI

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We characterized the potent in vitro antimalarial activity and biologic assessment of 13 phospholipid polar head analogs on a comparative basis. There was a positive relationship between the abilities of the drugs to inhibit parasite growth in culture and their abilities to specifically inhibit phosphatidylcholine biosynthesis of Plasmodium falciparum-infected erythrocytes. Maximal activity of G25 was observed for the trophozoite stage of the 48-h erythrocytic cycle (50% inhibitory concentration, 0.75 nM), whereas the schizont and ring stages were 12- and 213-fold less susceptible. The compounds exerted a rapid nonreversible cytotoxic effect, with complete clearance of parasitemia after 5 h of contact with the mature stages. The compounds were highly specific against P. falciparum, with much lower toxicity against three other mammalian cell lines, and the in vitro therapeutic indices ranged from 300 to 2,500,000. Finally, the monoquaternary ammonium E10 and two bis-ammonium salts, G5 and G25, were similarly active against multiresistant strains and fresh isolates of P. falciparum. This impressive selective in vitro toxicity against P. falciparum strongly highlights the clinical potential of these quaternary ammonium salts for malarial chemotherapy.

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Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI

Archives for Chemistry Experiments of 448-61-3

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In homogeneous catalysis, the catalyst is in the same phase as the reactant. The number of collisions between reactants and catalyst is at a maximum.In a patent, 448-61-3, name is 2,4,6-Triphenylpyrylium tetrafluoroborate, introducing its new discovery. Computed Properties of C23H17BF4O

A heterogeneous photocatalyst has been obtained by hosting the 2,4,6-triphenylpyrylium cation inside the supercages of Y-zeolite. Preparation of the new material has been achieved by means of a formal ion exchange in aqueous medium. Nevertheless, the mechanism is more complex, as bulky 2,4,6-triphenylpyrylium cation is unable to diffuse through the channels of Y-zeolite. The following steps are involved: (a) hydrolytic opening of the pyrylium ion to give a linear diketone; (b) diffusion of the diketone through the channels to reach the supercages; and (c) thermal recyclization under dehydrating conditions. Elemental analysis of the new material was consistent with the pyrylium cation located inside the zeolite. No sulfur was found in the loaded zeolite, indicating that hydrogensulfate is no longer the counter-ion of pyrylium. Accordingly, the stoichiometric amount of Na+ was found in the filtered waters recovered after the synthesis. Besides, the IR spectrum of the dry material was coincident with that of 2,4,6-triphenylpyrylium, while the spectrum of a less thoroughly dried sample showed, together with the absorption bands corresponding to pyrylium, other bands assignable to the diketone. Zeolite loading can be controlled in the range of 3-15% of organic carbon. The performance of the new material as a solar photocatalyst for oxidative pollutant degradation was checked using four cinnamic acid derivatives as target compounds. Aqueous solutions (250 mL) of these model pollutants (0.001 M) were irradiated by solar light in the presence of different amounts of solid photocatalyst. Oxidation was efficiently achieved as analysed by HPLC and followed in all cases a pseudo first order kinetics. The most satisfactory results were obtained using 1 g/L of Y-zeolite containing 6% of 2,4,6-triphenylpyrylium cation.

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Reference:
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI

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Electric Literature of 158014-74-5, Catalysts are substances that increase the reaction rate of a chemical reaction without being consumed in the process. 158014-74-5, Name is 4-([2,2′:6′,2”-Terpyridin]-4′-yl)benzoic acid, molecular formula is C22H15N3O2. In a Article,once mentioned of 158014-74-5

Electrocatalytic CO2reduction to CO was achieved with a novel Mn complex, fac-[MnBr(4,4?-bis(phosphonic acid)-2,2?-bipyridine)(CO)3] (MnP), immobilized on a mesoporous TiO2electrode. A benchmark turnover number of 112±17 was attained with these TiO2|MnP electrodes after 2 h electrolysis. Post-catalysis IR spectroscopy demonstrated that the molecular structure of the MnP catalyst was retained. UV/vis spectroscopy confirmed that an active Mn?Mn dimer was formed during catalysis on the TiO2electrode, showing the dynamic formation of a catalytically active dimer on an electrode surface. Finally, we combined the light-protected TiO2|MnP cathode with a CdS-sensitized photoanode to enable solar-light-driven CO2reduction with the light-sensitive MnP catalyst.

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Reference:
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI

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We identified a novel plasmid-borne gene (designated qacJ) encoding resistance to quaternary ammonium compounds (QACs) in three staphylococcal species associated with chronic infections in four horses. qacJ was located on a 2,650-bp plasmid (designated pNVH01), a new member of the pC194 family of rolling-circle replication plasmids. The 107-amino-acid protein, QacJ, showed similarities to known proteins of the small multidrug resistance family: Smr/QacC (72.5%), QacG (82.6%), and QacH (73.4%). The benzalkonium chloride MIC for a qacJ-containing recombinant was higher than those for otherwise isogenic recombinants expressing Smr, QacG, or QacH. Molecular epidemiological analyses by pulsed-field gel electrophoresis suggested both the clonal spread of a qacJ-harboring Staphylococcus aureus strain and the horizontal transfer of pNVH01 within and between different equine staphylococcal species. The presence of pNVH01 of identical nucleotide sequence in different staphylococcal species suggests that recent transfer has occurred. In three of the horses, a skin preparation containing cetyltrimethylammonium bromide had been used extensively for several years; this might explain the selection of staphylococci harboring the novel QAC resistance gene.

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Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI

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The interaction of a cationic dye crystal violet, in aqueous solution with different types of surfactants, such as anionic, cationic, non-ionic, gemini and their mixtures has been investigated spectrophotometrically and fluorimetrically in premicellar and post micellar concentration regions. In the premicellar concentration region of anionic surfactants, the dimer of the dye is formed; in the micellar concentration region, the monomer of the dye predominates. With cationic and nonionic surfactants, crystal violet is solubilised primarily as the monomer. In case of anionic and nonionic mixture, stability of dye-surfactant complex increases with increase in mole fraction of anionic surfactant. Cationic surfactant, cetyltrimethylammonium bromide (CTAB) has no interaction with crystal violet.

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Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI

Can You Really Do Chemisty Experiments About 4′-(4-Bromophenyl)-2,2′:6′,2”-terpyridine

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Catalysts function by providing an alternate reaction mechanism that has a lower activation energy than would be found in the absence of the catalyst. In some cases, the catalyzed mechanism may include additional steps.In a article, 89972-76-9, molcular formula is C21H14BrN3, introducing its new discovery. Application In Synthesis of 4′-(4-Bromophenyl)-2,2′:6′,2”-terpyridine

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Reference:
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI