Solutions solvents evaporation

The data plotted in Figure 3.6 were obtained by the fractionation of a polydisperse polymer sample. Polydisperse polymers can be fractionated by a number of techniques. The most widely used technique is chromatography. Other methods include addition of a nonsolvent to a polymer solution, cooling a polymer solution, solvent evaporation, extraction, diffusion, and centrifugation. The molecular weight of the fractions may be determined using any of the classic techniques given in Table 3.3. 

Fig. 6. Elimination coefficient versus temperature of casting solution at 0.06 MPa (1) 0.12 MPa (2) and 0.18 MPa (3) for membranes cast from 15 wt. % PS solution. Solvent evaporation time Os (A) 15s(B)...

Another highly suitable crystallization technique is adiabatic crystallization where the driving force for crystallization is the of super-saturation in the concentrated lactic acid solution brought about by heat neither being removed nor supplied. This involves lowering the temperature of the concentrated solution (solvent evaporates) and increasing the concentration of LA (two effects (a) solvent evaporates and (b) the temperature of the concentrated LA solution drops, as a result of which the solubility decreases and super-saturation may be resulted). 

Fig. 11.19 In a common implementation of the vapor diffusion method of biopolymer crystallization, a single drop of biopolymer solution hangs above a reservoir solution that is very concentrated in a nonvolatile solute. Solvent evaporates from the more dilute drop until the vapor pressure of water in the closed container reaches a constant equilibrium value.

Application of Solutions, Solvent Evaporates during Bonding. 

A drop of a dilute solution (1%) of an amphiphile in a solvent is typically placed on tlie water surface. The solvent evaporates, leaving behind a monolayer of molecules, which can be described as a two-dimensional gas, due to tlie large separation between tlie molecules (figure C2.4.3). The movable barrier pushes tlie molecules at tlie surface closer together, while pressure and area per molecule are recorded. The pressure-area isotlienn yields infonnation about tlie stability of monolayers at tlie water surface, a possible reorientation of tlie molecules in tlie two-dimensional system, phase transitions and changes in tlie confonnation. Wliile being pushed togetlier, tlie layer at... 

X)ml), The reaction mixture was stirred for 24 h. Nearly all of the solvent was removed in vacuo and the residue dissolved in CH2CI2. The solution was washed with 5% NHj, 1N HCl and brine. The organic layer was dried (NajSOJ and the solvent evaporated in vacuo. The residue was purified by chromatography using CHClj-hexane to give the product (28.0 g, 86%) along with a little 3-[2-nitro-2-(indol-3-ylmethyl)ethyl]indole (2.8 g. 5%). 

Samples of analyte are dissolved in a suitable solvent and placed on the IR card. After the solvent evaporates, the sample s spectrum is obtained. Because the thickness of the PE or PTEE film is not uniform, the primary use for IR cards has been for qualitative analysis. Zhao and Malinowski showed how a quantitative analysis for polystyrene could be performed by adding an internal standard of KSCN to the sample. Polystyrene was monitored at 1494 cm- and KSCN at 2064 cm-. Standard solutions were prepared by placing weighed portions of polystyrene in a 10-mL volumetric flask and diluting to volume with a solution of 10 g/L KSCN in... 

The passage of drops of solvent (S) containing a solute (M) through the evacuation chamber, the exit nozzle, skimmers 1 and 2, and into the ion chamber. Molecules of solvent evaporate throughout this passage, causing the drops to get smaller until only solute molecules remain. 

The particle beam — after linear passage from the evacuation chamber nozzle, through the first and second skimmers, and into the end of the ion source — finally passes through a heated grid immediately before ionization. The heated grid has the effect of breaking up most of the residual small clusters, so residual solvent evaporates and a beam of solute molecules enters the ionization chamber. 

An aerosol produced instrumentally has similar properties, except that the aerosol is usually produced from solutions and not from pure liquids. For solutions of analytes, the droplets consist of solute and solvent, from which the latter can evaporate to give smaller droplets of increasingly concentrated solution (Figure 19.1). If the solvent evaporates entirely from a droplet, the desolvated dry solute appears as small solid particles, often simply called particulate matter. 

Aerosols can be produced as a spray of droplets by various means. A good example of a nebulizer is the common household hair spray, which produces fine droplets of a solution of hair lacquer by using a gas to blow the lacquer solution through a fine nozzle so that it emerges as a spray of small droplets. In use, the droplets strike the hair and settle, and the solvent evaporates to leave behind the nonvolatile lacquer. For mass spectrometry, a spray of a solution of analyte can be produced similarly or by a wide variety of other methods, many of which are discussed here. Chapters 8 ( Electrospray Ionization ) and 11 ( Thermospray and Plasmaspray Interfaces ) also contain details of droplet evaporation and formation of ions that are relevant to the discussion in this chapter. Aerosols are also produced by laser ablation for more information on this topic, see Chapters 17 and 18. 

A flow of liquid, for example from high-performance liquid chromatography (HPLC), is treated in such a way that most of the solvent evaporates to leave solute molecules that pass into an ionization region (ion source). 

Figure 1.1 is a rather remarkable photograph which shows individual polystyrene molecules as spherical blobs having average diameters of about 20 nm. The picture is an electron micrograph in which a 10" % solution of polystyrene was deposited on a suitable substrate, the solvent evaporated, and the contrast enhanced by shadow casting. There is a brief discussion of both electron microscopy and shadowing in Sec. 4.7. Several points should be noted in connection with Fig. 1.1 ...

Genera.1 Ca.se, The simple adiabatic model just discussed often represents an oversimplification, since the real situation implies a multitude of heat effects (/) The heat of solution tends to increase the temperature and thus to reduce the solubihty. 2) In the case of a volatile solvent, partial solvent evaporation absorbs some of the heat. (This effect is particularly important when using water, the cheapest solvent.) (J) Heat is transferred from the hquid to the gas phase and vice versa. (4) Heat is transferred from both phase streams to the shell of the column and from the shell to the outside or to cooling cods. 

Solution Properties. Typically, if a polymer is soluble ia a solvent, it is soluble ia all proportions. As solvent evaporates from the solution, no phase separation or precipitation occurs. The solution viscosity iacreases continually until a coherent film is formed. The film is held together by molecular entanglements and secondary bonding forces. The solubiUty of the acrylate polymers is affected by the nature of the side group. Polymers that contain short side chaias are relatively polar and are soluble ia polar solvents such as ketones, esters, or ether alcohols. As the side chaia iacreases ia length the polymers are less polar and dissolve ia relatively nonpolar solvents, such as aromatic or aUphatic hydrocarbons. 

Solution Polymers. Acryflc solution polymers are usually characterized by their composition, solids content, viscosity, molecular weight, glass-transition temperature, and solvent. The compositions of acryflc polymers are most readily determined by physicochemical methods such as spectroscopy, pyrolytic gas—liquid chromatography, and refractive index measurements (97,158). The solids content of acryflc polymers is determined by dilution followed by solvent evaporation to constant weight. Viscosities are most conveniently determined with a Brookfield viscometer, molecular weight by intrinsic viscosity (158), and glass-transition temperature by calorimetry. 

The heated polymer solution emerges as filaments from the spinneret into a column of warm air. Instantaneous loss of solvent from the surface of the filament causes a soHd skin to form over the stiU-Hquid interior. As the filament is heated by the warm air, more solvent evaporates. More than 80% of the solvent can be removed during a brief residence time of less than 1 s in the hot air column. The air column or cabinet height is 2—8 m, depending on the extent of drying required and the extmsion speed. The air flow may be concurrent or countercurrent to the direction of fiber movement. The fiber properties are contingent on the solvent-removal rate, and precise air flow and temperature control are necessary. 

Sir Joseph Swan, as a result of his quest for carbon fiber for lamp filaments (2), learned how to denitrate nitrocellulose using ammonium sulfide. In 1885 he exhibited the first textiles made from this new artificial sHk, but with carbon fiber being his main theme he failed to foUow up on the textile possibihties. Meanwhile Count Hilaire de Chardoimet (3) was researching the nitrocellulose route and had perfected his first fibers and textiles in time for the Paris Exhibition in 1889. There he got the necessary financial backing for the first Chardoimet silk factory in Besancon in 1890. His process involved treating mulberry leaves with nitric and sulfuric acids to form cellulose nitrate which could be dissolved in ether and alcohol. This collodion solution could be extmded through holes in a spinneret into warm air where solvent evaporation led to the formation of soHd cellulose nitrate filaments. 

Phase Inversion (Solution Precipitation). Phase inversion, also known as solution precipitation or polymer precipitation, is the most important asymmetric membrane preparation method. In this process, a clear polymer solution is precipitated into two phases a soHd polymer-rich phase that forms the matrix of the membrane, and a Hquid polymer-poor phase that forms the membrane pores. If precipitation is rapid, the pore-forming Hquid droplets tend to be small and the membranes formed are markedly asymmetric. If precipitation is slow, the pore-forming Hquid droplets tend to agglomerate while the casting solution is stiU fluid, so that the final pores are relatively large and the membrane stmcture is more symmetrical. Polymer precipitation from a solution can be achieved in several ways, such as cooling, solvent evaporation, precipitation by immersion in water, or imbibition of... 

Fig. 10. Schematic of casting machine used to make microporous membranes by watervapor imbibition. A casting solution is deposited as a thin film on a moving stainless steel belt. The film passes through a series of humid and dry chambers, where the solvent evaporates from the solution, and water vapor is absorbed from the air. This precipitates the polymer, forming a microporous membrane that is taken up on a collection roU (25).

Fig. 13. Phase diagram showing the composition pathway traveled by a casting solution during the preparation of porous membranes by solvent evaporation. A, initial casting solution B, point of precipitation and C, point of soHdification. See text.

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