Bubble Apparatus

For gas-liquid combinations with relatively small uptake coefficients ( 10 4-10-7), longer interaction times between the gas and liquid are needed than can be obtained with the falling-droplet apparatus. These are provided in a bubble apparatus, a typical example of which is shown in Fig. 5.24. The gas of interest as a mixture with an inert carrier gas is introduced as a stream of bubbles into the liquid of interest. The interaction time is varied by moving the gas injector relative to the surface. The composition of the gas exiting the top of the liquid is measured as a function of the interaction time (typically 0.1-1 s), e.g., by mass spectrometry. The interaction time is limited by the depth in the liquid at which the bubbles are injected and their buoyancy. Longer interaction times and better control over them have been achieved using a modified apparatus in which the bubbles are generated and transported horizontally (Swartz et a.l., 1997). 

FIGURE 5.24 Schematic of bubble apparatus (adapted from Shorter et at., 1995). 

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The contact angles at the quartz- (or glass) water-air interface were measured using a modified captive-bubble apparatus (1). 

Hold the tube horizontally and quickly seal this end in a micro-burner. Attach the tube (with the open end upwards) to a thermometer in the melting-point apparatus (Fig. i(c), p. 3) so that the trapped bubble of air in the capillary tube is below the surface of the bath-liquid. Now heat the bath, and take as the b.p. of the liquid that temperature at which the upper level of the bubble reaches the level of the surface of the batn liquid. 

Fig. 32). Using a fine pipette insert about i cm. length of the liquid into the bottom of the tube. Now place in the tube A a fine inverted melting-point tube B of about i mm. diameter, sealed at the upper end. Fasten the capillary tube to the ther- Fio. 32. mometer by means of a rubber band and place in a melting-point apparatus. Heat slowly until a stream of bubbles rises from the bottom... 

The fiimace E is now switched on, and takes about 20 minutes before the combustion tube packing has reached the required temperature. After 15 minutes, carbon dioxide is again passed for 5 minutes, and the apparatus tested as before for the appearance of micro-bubbles. If these are not at first obtained, the sweeping-out process must be continued until they do appear. Now that the combustion-tube packing is heated up to the required temperature and the apparatus filled with carbon dioxide, all air being swept out, the combustion may be started. 

In order to carry out a distillation, the apparatus is completely assembled, the water pump turned on to its maximum capacity, and the screw clip on the capillary tube in the Claisen flask adjusted so that a gentle stream of air bubbles through the liquid (see Section 11,19 for details of the preparation of the capillary tube). The barometric pressure is read, and if the resulting vacuum deter mined from the reading on the mano meter is satisfactory (as estimated from the temperature of the tap water), the flask may be heated in an air (Fig. II,... 

Carbonate ionophore I [ETH 6010] (heptyl 4-trifluoroacetylbenzoate) [129476-47-7] M 316.3, b 170°/0.02 Torr, d 0.909. Purified by flash chromatography (2g of reagent with 30g of Silica Gel 60) and eluted with EtOAc/hexane (1 19). The fractions that absorbed at 260nm were pooled, evapd and dried at room temp (10.3 Torr). The oily residue was distd in a bubbled-tube apparatus (170°/0.02 Torr). Its IR (CHCI3) had peaks at 1720, 1280, 940cm and its sol in tetrahydrofuran is 50mg/0.5mL. It is a lipophilic neutral ionophore selective for carbonate as well as being an optical humidity sensor. [Anal Chim Acta 233 41 1990.]... 

Methyl trichlorosilane [75-79-6] M 149.5, b 13,7 /101mm, 64.3 /710.8mm, 65.5 /745mm, 66.1 /atm, d 1.263, n 1.4110. If very pure distil before use. Purity checked by Si nmr, 6 in MeCN is 13.14 with respect to Me4Si. Possible contaminants are other silanes which can be removed by fractional distillation through a Stedman column of >72 theoretical plates with total reflux and 0.35% take-off (see p. 441). The apparatus is under N2 at a rate of 12 bubbles/min fed into the line using an Hg manometer to control the pressure. Sensitive to H2O. [J Am Chem Soc 73 4252 7957 J Org Chem 48 3667 7955.]... 

The term still is applied only to the vessel in which liquids are boiled during distillation, but the term is sometimes applied to the entire apparatus, including the fractionating column, the condenser, and the receiver in which the distillate is collected. If a water and alcohol distillate is returned from the condenser and made to drip down through a long column onto a series of plates, and if the vapor, as it rises to the condenser, is made to bubble through this liquid at each plate, the vapor and liquid will interact so that some of the water in the vapor condenses and some of the alcohol in the liquid vaporizes. The interaction at each plate is equivalent to a redistillation. This process is referred to by several names in the industry namely rectification, fractionation, or fractional distillation. 

It must now be tested to see that it is air-tight. For this purpose, close the open end of the potash apparatus with a tight stopper and turn on the full pressure from either gasholder. After the first few bubbles of air have passed through the bulbs of the potash apparatus no further movement of bubbles should appear in any art of the apparatus. If it withstands this test, the combustion may proceed. Release the pressure by closing the tap of the gas-holder, screwing i p the... 

Whilst the water is boiling steadily and not too violently, the substance is weighed. Chloroform, b.p. 61, or pure and dry ether, bp. 34-5° (see Prep. 3, p 59), may be used for the experiment, as their boiling-points he well below that of water. Before introducing the bottle and liquid, the apparatus must be tested to ascertain if the temperatur e is constant. As a rule hour s boiling suffices. Push in the rubber cork and note if within the next minute or two any bubbles csc.rije. If... 

Blase,/, bubble, bleb blister, vesicle cavity (Metal.) blowhole bladder bladder-shaped vessel, as the body of a retort or still still. Blaae-. blowing, blast, -apparat, m. still blast apparatus, -balg, m. bellows, -lampe, /. blast lamp. 

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