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Hydrogen, bubbles

Most of the voltage savings in the air cathode electrolyzer results from the change in the cathode reaction and a reduction in the solution ohmic drop as a result of the absence of the hydrogen bubble gas void fraction in the catholyte. The air cathode electrolyzer operates at 2.1 V at 3 kA/m or approximately 1450 d-c kW-h per ton of NaOH. The air cathode technology has been demonstrated in commercial sized equipment at Occidental Chemical s Muscle Shoals, Alabama plant. However, it is not presentiy being practiced because the technology is too expensive to commercialize at power costs of 20 to 30 mils (1 mil = 0.1 /kW). [Pg.500]

Experimental techniques to visualize flows have been extensively used to define fluid flow in pipes and air flow over lift and control surface of airplanes. More recently this technology has been appHed to the coating process and it is now possible to visualize the flow patterns (16,17). The dimensions of the flow field are small, and the flow patterns both along the flow and inside the flow are important. Specialized techniques such as utilizing small hydrogen bubbles, dye injection, and optional sectioning, are required to visualize these flows. [Pg.313]

Thomas and Rice [/. Appl. Mech., 40, 321-325 (1973)] applied the hydrogen-bubble technique for velocity measurements in thin hquid films. DureUi and Norgard [Exp. Mech., 12,169-177 (1972)] compare the flow birefringence and hydrogen-bubble techniques. [Pg.889]

Suspension of fine solid particles m a liquid, such as m the catalytic hydrogenation of a liquid where solid catalyst and hydrogen bubbles are dispersed m the liquid. [Pg.554]

L. W. Alvarez (Berkeley) decisive contributions to elementary particle physics, in particular the discovery of a large number of resonance states, made possible by the hydrogen bubble chamber technique and data analysis. [Pg.1302]

Where R is the gas constant, T the temperature (K), Fthe Faraday constant and H2 is the relative partial pressure (strictly, the fugacity) of hydrogen in solution, which for continued evolution becomes the total external pressure against which hydrogen bubbles must prevail to escape (usually 1 atm). The activity of water a jo is not usually taken into account in elementary treatments, since it is assumed that <7h2 0 = U nd for dilute solutions this causes little error. In some concentrated plating baths Oh2 0 I O nd neither is it in baths which use mixtures of water and miscible organic liquids (e.g. dimethyl formamide). However, by far the most important term is the hydrogen ion activity this may be separated so that equation 12.1 becomes... [Pg.340]

The flow patterns for single phase, Newtonian and non-Newtonian liquids in tanks agitated by various types of impeller have been repotted in the literature.1 3 27 38 39) The experimental techniques which have been employed include the introduction of tracer liquids, neutrally buoyant particles or hydrogen bubbles, and measurement of local velocities by means of Pitot tubes, laser-doppler anemometers, and so on. The salient features of the flow patterns encountered with propellers and disc turbines are shown in Figures 7.9 and 7.10. [Pg.294]

The reaction at Eq. (12) allows the preparation of Na2S4 and K2S5 from the alkali metals, hydrogen sulfide and sulfur in anhydrous ethanol (ROH). First the metal is dissolved in the alcohol with formation of ethanolate (MOR) and hydrogen. Bubbling of H2S into this solution produces the hydrogen sulfide (MHS). To obtain the polysulfide the solution is refluxed with the calculated amount of elemental sulfur. After partial evaporation of the solvent and subsequent cooling the product precipitates. [Pg.131]

Fig. 4.3 SEM micrograph of the rear side of an n-(lOO) Si wafer polished on one side. The presence of inverted truncated square pyramidal stmctures fuUy covering the surface can be observed. This pyramidal texturing was attributed to the combination of anisotropic etching of the sdicon and to hydrogen bubbles evolved during the etching reaction. (Reprinted from [23] Copyright 2009, with permission from Elsevier)... Fig. 4.3 SEM micrograph of the rear side of an n-(lOO) Si wafer polished on one side. The presence of inverted truncated square pyramidal stmctures fuUy covering the surface can be observed. This pyramidal texturing was attributed to the combination of anisotropic etching of the sdicon and to hydrogen bubbles evolved during the etching reaction. (Reprinted from [23] Copyright 2009, with permission from Elsevier)...
Add sodium borohydride (Aldrich) to the peptide solution to obtain a final concentration of 0.1M. Generation of hydrogen bubbles will occur as the borohydride is dissolved. [Pg.100]

Adjust the pH of the reaction to pH 4.0 using dilute HC1. Incubate for 10 minutes to assure the complete destruction of excess borohydride. Hydrogen bubbles again will be evolved from the solution. [Pg.100]

In a fume hood, dissolve 125 mg of sodium cyanoborohydride in 1ml water (makes a 2M solution). Caution Highly toxic compound handle with care. This solution may be allowed to sit for 30 minutes to eliminate most of the hydrogen-bubble evolution that could affect the vesicle suspension. [Pg.894]

So far only aqueous solutions have been considered however, mixtures of HF and ethanol or methanol are quite common, because this addition reduces the surface tension and thereby the sticking probability of hydrogen bubbles. While substantial quantities of ethanol or methanol are needed to reduce the surface tension, cationic or anionic surfactants fulfill the same purpose in concentrations as low as 0.01 M [So3, Chl6]. [Pg.11]

Defects in a SCR, which is present under reverse bias, can be tested in a similar way. Figure 10.6 c shows the same wafer as in Fig. 10.6 e after removal of the oxide and under cathodic polarization in the dark. Hydrogen bubbles caused by the dark current now decorate nickel silicide precipitates that short-circuit the SCR. Nickel precipitates are known to increase the dark current of a p-type Si electrode under reverse bias by orders of magnitude [Wa4]. If the bias is increased the copper silicide precipitates also become visible, as shown in Fig. 10.6 d. This method, like defect etching (Fig. 10.4f), is only sensitive to precipitated metals. Metals that stay in solution, like iron, do not show up in defect mapping and have to be determined by other methods, for example diffusion length mapping. [Pg.217]

If mapping of the defects is dispensable and only the average contamination level is of interest, measurements of the reverse dark current are sufficient to provide this information [Wi2]. This method is also applicable to n-type samples, which is in contrast to decoration of SCR defects by hydrogen bubbles, which is not possible in the anodic regime. [Pg.217]

Fig. 10.6 A p-type Si wafer with a 20 nm thick thermal oxide has been contaminated by scratching the backside with metal wires (Ni, Cu, Fe), according to the pattern shown in (a) and later annealed at 1200°C for 30 s. (e) Under cathodic bias in acetic acid, oxide defects become decorated by hydrogen bubbles. (c, d) After oxide removal junction defects caused by metal precipitates are decorated by hydrogen bubbles, if sufficient catho... Fig. 10.6 A p-type Si wafer with a 20 nm thick thermal oxide has been contaminated by scratching the backside with metal wires (Ni, Cu, Fe), according to the pattern shown in (a) and later annealed at 1200°C for 30 s. (e) Under cathodic bias in acetic acid, oxide defects become decorated by hydrogen bubbles. (c, d) After oxide removal junction defects caused by metal precipitates are decorated by hydrogen bubbles, if sufficient catho...
The hot effluent from the reactor containing acetone, unreacted IPA, and hydrogen is cooled in a condenser and then scrubbed with water to remove the hydrogen. Both IPA and acetone are highly soluble in water, but hydrogen is not. So, by washing the effluent with water, the hydrogen bubbles out the top, and the IPA/acetone comes out the bottom with the water. [Pg.241]

Previous work on the application of the acoustic emission technique to corrosion processes has been carried out by Mansfeld and Stocker (i) who were able to show that the detachment of hydrogen bubbles from a polarised metal surface gave measurable signals. [Pg.115]

In the previous problem the hydrogen bubbles are initially 0.1 cm in diameter, and they contain pure H2 gas at a concentration of 0.05 moles/cm (which does not change as the bubbles rise). Hydrogen is transferred from the bubbles to the liquid with a rate limited by mass transfer (k, = Dyi lR) in the liquid around the bubble with Dq, = 1 x 10 cm /sec. There is no reaction in the bubbles. [Pg.518]

She dropped a magnesium strip and an iron nail into a 6M solution of HCI. The magnesium strip produced more hydrogen bubbles than the iron nail. [Pg.235]

Bhaga (B3) determined the fluid motion in wakes using hydrogen bubble tracers. Closed wakes were shown to contain a toroidal vortex with its core in the horizontal plane where the wake has its widest cross section. The core diameter is about 70% of the maximum wake diameter, similar to a Hill s spherical vortex. When the base of the fluid particle is indented, the toroidal motion extends into the indentation. Liquid within the closed wake moves considerably more slowly relative to the drop or bubble than the terminal velocity Uj, If a skirt forms, the basic toroidal motion in the wake is still present (see Fig. 8.5), but the strength of the vortex is reduced. Momentum considerations require that there be a velocity defect behind closed wakes and this accounts for the tail observed by some workers (S5). Crabtree and Bridgwater (C8) and Bhaga (B3) measured the velocity decay and drift in the far wake region. [Pg.211]

Various improved methods for making STM tips linked with SEM studies have been discussed in the literature, for example, Lemke (1990), Melmed (1991), and references therein. However, since the STM resolution does not have a direct correlation with the look of the tip under SEM, the simple dc dropoff method, as described here, is usually sufficient. From the experience of the author, two simple improvements can be helpful. The first is to install an insulating piece between the cathode and anode across the liquid surface to prevent the hydrogen bubbling on the cathode from perturbing the meniscus near the anode. The second is to save the dropped piece as the tip, which might be better than the upper one. [Pg.284]


See other pages where Hydrogen, bubbles is mentioned: [Pg.309]    [Pg.527]    [Pg.313]    [Pg.889]    [Pg.16]    [Pg.163]    [Pg.337]    [Pg.528]    [Pg.529]    [Pg.315]    [Pg.1615]    [Pg.173]    [Pg.75]    [Pg.234]    [Pg.165]    [Pg.234]    [Pg.13]    [Pg.29]    [Pg.42]    [Pg.204]    [Pg.217]    [Pg.301]    [Pg.244]    [Pg.105]    [Pg.117]    [Pg.518]    [Pg.212]    [Pg.339]   
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