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n octanol/кариес

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СтатииКлинични изследванияПатенти
7 резултата

Influence of n-octanol and α-terpineol on thin film stability and bubble attachment to hydrophobic surface.

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We have investigated the influence of concentration of surfactants typically used as flotation frothers (α-terpineol and n-octanol) and roughness of the solid surface on phenomena occurring during rising bubble collisions with a model hydrophobic Teflon surface. The time of three-phase contact (TPC)

Spin exchange in solutions of TEMPOL in n-octanol and 1-methyl-3-octylimidazolium hexafluorophosphate in the temperature range from 300 to 500 K.

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Comprehensive examinations of the motional properties (rotational correlation time τ(R)) and the spin exchange ω(SS) of the spin probe TEMPOL have been carried out using ESR spectroscopy in two different solvents. For the first time, the dynamic parameters τ(R) and ω(SS) have been determined

In vitro inhibition potential of mono-n-octyl phthalate on Mycobacterium tuberculosis H37Ra: Possibility of binding to mycobacterial PknB-An in silico approach.

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Fatty acids of specific chain lengths have been shown to inhibit the growth of Mycobacterium tuberculosis. In the present study, specific synthetic aromatic derivatives of n-octyl esters were investigated for their property to inhibit the growth of M. tuberculosis H37Ra. Agar well diffusion assay

Ballpoint connector-protected salt-oil-salt liquid phase microextraction for concentration and enrichment of trace anthraquinone compounds in rhubarb.

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This study proposed a new ballpoint connector-protected salt-oil-salt liquid phase microextraction for extraction and enrichment of trace rhein and chrysophanol in rhubarb prior to determination of the analytes by high performance liquid chromatography. In this study, a handy ballpoint connector

A Non-catalytic Deep Desulphurization Process using Hydrodynamic Cavitation.

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A novel approach is developed for desulphurization of fuels or organics without use of catalyst. In this process, organic and aqueous phases are mixed in a predefined manner under ambient conditions and passed through a cavitating device. Vapor cavities formed in the cavitating device are then

Simple physics-based analytical formulas for the potentials of mean force for the interaction of amino acid side chains in water. IV. Pairs of different hydrophobic side chains.

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The potentials of mean force of 21 heterodimers of the molecules modeling hydrophobic amino acid side chains: ethane (for alanine), propane (for proline), isobutane (for valine), isopentane (for leucine and isoleucine), ethylbenzene (for phenylalanine), methyl propyl sulfide (for methionine), and

Iodine emission in the presence of humic substances at the water's surface.

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Humic substances that preferentially adsorb at the air/water interfaces of water or aerosols consist of both fulvic and humic acid. To investigate the chemical reactivity for the heterogeneous reaction of gaseous ozone, O(3)(g), with aqueous iodide, I(-)(aq), in the presence of standard fulvic acid,
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