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Organic solvents methylethylketone

Plummer invented a process for the biodesulfurization of hydrocarbons [157], in which organic sulfur compounds contained in liquid hydrocarbons are converted to elemental sulfur. The reaction is carried out in the presence of a biocatalyst and hydrogen, by dissolving completely the liquid hydrocarbons in an organic solvent, such as a nucleophilic and/or electrophilic solvent(s). The nucleophilic solvent should have a pKa greater than 2, and the electrophilic solvent more negative than -2. Recommended nucleophilic solvents include -butylamine, diethylamine, butanediamine, ethylenimine, toluene, pyridine, aniline, and acetophenone. The electrophilic solvents could be methylethylketone, pyrrole, or benzaldehyde. [Pg.356]

P.Y.173, an isoindolinone pigment, affords somewhat dull, greenish yellow shades. It shows average fastness to organic solvents, especially to alcohols (ethanol), esters (ethyl acetate), and ketones (including methylethylketone and cyclohexanone). Its solvent resistance equals step 3 on the 5 step scale. P.Y.173 is almost completely to completely fast to mineral spirits and xylene. [Pg.415]

P.Y.182, which has been available for some years, provides somewhat reddish shades of yellow and is tinctorially strong. It is sensitive to a variety of organic solvents, especially to ketones such as methylethylketone and cyclohexanone, as well as to aromatic solvents such as toluene or xylene. In this respect, the pigment equals step 2 on the 5-step scale (Sec. 1.6.2.1). P.Y.182 is targeted for the paint and the plastics industry. [Pg.572]

Epoxynovolak resin and BPA/DC-BMI prepolymer, tert.butyl peroxide and Zn acetate [106, 107] or 2-phenylimidazole and other catalysts [108] were filled with wollastonite. Carbon-fiber reinforced composites were obtained using a binder, which consisted of BPA/DC, BMI, an epoxynovolak, 2-ethyl-4-methylimidazole and an organic solvent [109]. A BPA/DC-BMI prepolymer in methylethylketone was mixed with middle-molecular-weight epoxide resin (Epikote 1001), 2-ethyl-4-methyl-imidazole, Zn acetate and triethylenediamine thermal shock resistant GRP was thus obtained [110]. [Pg.54]

Figure 1 gives a typical infrared spectrum of lake humic acid. The interpretation of infrared spectra of humic substances is discussed in depth by -MacCarthy and Rice in Chapter 21. The similarity of infrared spectra of humic acids from different lakes suggests a similarity of the aspects of chemical structure that are related to their infrared absorptions. However, infrared spectroscopy is not sensitive enough to uncover minor structural differences among humic acids. In fact, humic acids were separated by organic solvents (chloroform, methylethylketone, methanol, dimethylformamide) into various fractions (Ishiwatari, 1969b, 1973). Infrared spectra of two of these fractions, the chloroform-soluble fraction and the methylethylketone-... [Pg.155]

Several organic solvents were investigated, including dichloromethane, chloroform, ethyl acetate, acetone, methylethylketone, tetrahydrofuran, acetonitrile, and mixtures thereof, but only water-insoluble solvents were suited for dissolving polymer and phospholipid in high concentrations and forming spherical particles in good yield. [Pg.7]

Sparingly soluble in water, soluble in organic solvents such as ethanol, acetone, methylethylketone, benzene, toluene, xylene Stable in a pH range of 3-11 decomposition at 230-240°C... [Pg.50]


See other pages where Organic solvents methylethylketone is mentioned: [Pg.195]    [Pg.208]    [Pg.304]    [Pg.353]    [Pg.393]    [Pg.397]    [Pg.196]    [Pg.835]    [Pg.241]    [Pg.207]    [Pg.129]    [Pg.4]    [Pg.12]    [Pg.470]    [Pg.30]    [Pg.154]    [Pg.273]   
See also in sourсe #XX -- [ Pg.4 ]




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METHYLETHYLKETONE

Methylethylketon

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