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Thinning solvent

With the ever increasing awareness of the need of environment protection, the emission of solvent vapors and organic fumes into the atmosphere should be prevented by treating the exhaust through a proper scmbber. The solvent used for cleaning the reactor is usually consumed as part of the thinning solvent. Aqueous effluent should be properly treated before discharge. [Pg.41]

Ergometrine crystallises, with solvent, from benzene in needles or from methyl ethyl ketone in prisms both forms have m.p. 162-3° (dec.). From ethyl acetate it crystallises at — 4° in thin, solvent-free plates, m.p. 160-1° (dec.), and at atmospheric temperature on concentration in vacuo in diamond-shaped plates, B.0-5EtAc, m.p. 130-2° (dec.), from which the combined solvent is not removed at 100° in vacuo. By crystallisation from acetone, Grant and Smith obtained a second form in long needles, m.p. 212° (dec.), which appears to be the more stable, since the form, m.p. 162-3°, tends to pass into it on keeping. Ergometrine has [o]d — 44° (CHCI3) - - 42-2° or + 62-6° (c = 1-7, EtOH) or... [Pg.524]

Mechanical Properties. The mechanical properties of thin, solvent-cast polymer films were measured on an Instron Tensile Tester according to ASTM standard D882-83. In all cases, tensile values were calculated from the average of at least four measurements obtained from four separate specimens per polymer sample. [Pg.157]

Solvent mixtures that contain heat-sensitive compounds, are viscous, or have high boihng points can be separated using wiped-film evaporators (WFE) [57, 58]. A WFE operates by receiving a liquid feed into a column that contains several wiper blades. The walls of the WFE are heated at a constant temperature in order to vaporize the solvent film. As the solvent vapors migrate to the center of the WFE, they come into contact with a coohng unit that condenses the vapors, allowing them to flow down the condenser to the outlet receiver. The thin solvent film and reduced system pressure (in the case of vacuum operation) allows the solvents to be separated slowly at lower temperatures [57-59]. [Pg.78]

Figure 4. ESCA Cls spectra for a thin, solvent-deposited film of PEEK on copper metal at temperatures from 30°C to 350°C. Figure 4. ESCA Cls spectra for a thin, solvent-deposited film of PEEK on copper metal at temperatures from 30°C to 350°C.
Figure 5. The X-ray induced Auger L3W spectra for a thin, solvent-... Figure 5. The X-ray induced Auger L3W spectra for a thin, solvent-...
Fig. 5. Tapping Mode pictures of a thin solvent-cast copolymer film with 20 (left) and 30 (right) wt% of a siloxane macromonomer. Clearly seen is the transition fi om a segregated domain stmeture to an interpenetrating sponge morphology. Fig. 5. Tapping Mode pictures of a thin solvent-cast copolymer film with 20 (left) and 30 (right) wt% of a siloxane macromonomer. Clearly seen is the transition fi om a segregated domain stmeture to an interpenetrating sponge morphology.
In analogy to the relation between SPE and SPME discussed below, a refinement of LEE is achieved by the LLLME method. Analytes in a stirred matrix solution (the donor) are extracted into a thin solvent film filling the pores in the walls of a hollow fiber and diffuse into a collecting solution (the acceptor) filling the inner void of the hollow fiber. The enrichment factor depends not only on the volume ratio between the donor and the acceptor, but also on the operational conditions. The main advantages of the method are simplicity of operation, low cost, the scarce use of organic solvents and avoidance of evaporation operations120. [Pg.662]

Fig. 1 Optical spectra of alkali metal solutions in ethylenediamine (8), corrected for sodide absorption (bottom) and from thin solvent-free fihns (top). The solution spectrum labeled e is that of lithium. Note also the shoulder due to ejoiv in Cs. Rb. and K solutions. Fig. 1 Optical spectra of alkali metal solutions in ethylenediamine (8), corrected for sodide absorption (bottom) and from thin solvent-free fihns (top). The solution spectrum labeled e is that of lithium. Note also the shoulder due to ejoiv in Cs. Rb. and K solutions.
Degradation time constant for thin, solvent cast films under simulated physiological conditions (37°C, pH 7.4 PBS). [Pg.263]

Naphtha A petroleum distillate used mostly by professionals (as opposed to do-it-yourself painters) for cleanup and to thin solvent-based eoatings. A volatile organic compound (see VOC). [Pg.24]

Cubic BN powders (usually < 0.5 mm in size) are produced when hBN powders mixed with solvent powders are subjected to pressure > 5 GPa and temperatures > 1500°C for several minutes. Commercial cBN powders are mass produced in this way. For diamond synthesis by the high-pressure film method, described in Sec. IV.A.1, a thin solvent film always exists between the graphite source material and the diamond crystal produced. The formation mechanism of cBN powders is believed to be the same as that for the synthesis of diamond by the high-pressure film method, although a solvent film between the hBN source material and the cBN crystal produced has not been observed as clearly as it has been for diamond (223). [Pg.532]


See other pages where Thinning solvent is mentioned: [Pg.71]    [Pg.96]    [Pg.39]    [Pg.222]    [Pg.24]    [Pg.217]    [Pg.4]    [Pg.1033]    [Pg.2380]    [Pg.1033]    [Pg.99]    [Pg.269]    [Pg.106]    [Pg.1430]    [Pg.274]    [Pg.635]    [Pg.503]    [Pg.111]    [Pg.337]    [Pg.232]    [Pg.727]    [Pg.176]   
See also in sourсe #XX -- [ Pg.232 ]




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