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Bowl

Figure 3.5 shows centrifuges in which a cylindrical bowl is rotated to produce the centrifugal force. In Fig. 3.5a, the cylindrical bowl is shown rotating with a feed consisting of a solid-liquid mixture admitted at the center. The feed is immediately thrown outward toward the walls of the container. The particles settle horizontally... [Pg.72]

Figure 3 A centrifuge uses a rotating bowl to produce centrifugal force. Figure 3 A centrifuge uses a rotating bowl to produce centrifugal force.
Bowles R S ef a/1981 Generation of moleoular olusters of oontrolled size Surf. Sc/. 106 117... [Pg.2918]

Wc must add the amount of energy at the bottom of the bowl" in Fig. 10-lb to the siirri fix)rri Exercise 10-5. This energy is one-half a quantum at the wavenumber extrapr)lated rnie-half quantum number below n 0 (see Pn)blerns). [Pg.303]

The best replacement for borosilicate glassware is stainless steel. Stainless steel takes the heat, won t break, and, most importantly, is about as resistant to chemical degradation as the chemist can hope to find. For those items that won t be subjected to direct heat there can be some steel/metal or steel/plastic hybrids. In figure 3 is shown how flasks of any size can be made with two stainless steel mixing bowls welded together. Also shown is the vacuum adaptor and condenser. For the condenser only the inner pipe need be steel. The outside pipe can be copper or something. As for the other components of a distillation set up, well, they are made just as they look. [Pg.19]

Cut the blanched bacon strips in half. Place one jalapeno half against 1 shrimp, wrap with a bacon piece and secure with a toothpick. Place all of the shrimp brochettes into a bowl and marinated at least 30 minutes covered with teriyaki sauce. Broil 5 minutes and serve. Yum ... [Pg.161]

Alternate beef and shrimp on skewers. Mix the peanut oil, soy sauce and lime juice in a bowl to use a basting sauce. On a nice, hot coai or wood grill, cook the k-bobs until medium rare (or to taste) brushing them often with the basting liquid. Put aside and keep warm. [Pg.162]

DMSO - Dimethylsulphoxide is a very common solvent with a freezing point of 20 degrees. When you buy this stuff it will be crystallised in the bottle. To melt, all you need to do is place the bottle in a bowl of hot water for 30 minutes - simple. If you re lucky enough to live somewhere warm it may already be liquid, where I live, no chance. When you open the bottle you will notice that this stuff smells a bit farty, don t worry too much, it doesn t get that bad. 500ml straight into the reaction flask and start the stirrer. [Pg.218]

NOTE In order to make this as painless as possible, please observe the following recommendations 1) Keep the mixing bowl temperature as close to OC or less as possible 2) Keep the Hypochlorite solution as it is being added as close to OC or less as possible 3) After half the Hypochlorite solution has been added, place a plastic bag with 50-1 OOg ice/salt/water mix into the bowl to help keep temperatures low (use this instead of directly adding ice to the reactants, which adds a considerable volume of water making the process less volumetric ally efficient) 4) Purchase an 81b bag of ice ahead of time ... [Pg.262]

This last solution should be prepared slowly as it is quite exothermic. Set all three aside in a freezer. Now prepare the mixing apparatus which will be a stainless steel "mixing bowl" suspended In the ice/salt bath made earlier. We use a stainless steel bowl here so that heat transfer will be maximal, while preventing any corrosive interaction. A glass bowl will not be sufficient for larger scale preparations as it will not conduct heat fast enough to prevent the reactants from going over IOC (at which point the Haloamide will decompose and you ll have to start over). Take the Sodium Hydroxide solution out of the freezer once it is cool, but not cold. [Pg.262]

Preheat a water bath on the stove (or wherever) to about 80C and place the stainless steel mixing bowl in it. Once the temperature of the solution hits about 65C, take the bowl out and set aside while stirring all the while. This is where it rearranges, and the reaction is exothermic enough to sustain it s temperature nicely. If you find the temperature climbing past 80C, immerse the bowl into some cold waiter briefly. After about 15 minutes the temperature will start to fall, at which point you should transfer the whole mess to the distilling flask. Before you continue you need to choose whether you want to make the hydrochloride salt or the aqueous solution of Methylamine, though. [Pg.263]

Figure 6.15 The infrared vibrational spectrum of crotonaldehyde. The parts marked (a), (b) and (c) refer to a 10 per cent (by volume) solution in CCI4, a 1 per cent solution in CCI4, and a thin liquid film, respectively. [Reproduced, with permission, from Bowles, A. J., George, W. O. and Maddams, W. F J. Chem. Soc. (B), 810, 1969]... Figure 6.15 The infrared vibrational spectrum of crotonaldehyde. The parts marked (a), (b) and (c) refer to a 10 per cent (by volume) solution in CCI4, a 1 per cent solution in CCI4, and a thin liquid film, respectively. [Reproduced, with permission, from Bowles, A. J., George, W. O. and Maddams, W. F J. Chem. Soc. (B), 810, 1969]...
Togaviridae Toilet bowls Toilet preparations Toiletries Toiletry products Tokamaks Tokamax Tolazamide... [Pg.1000]

A method for the fractionation of plasma, allowing albumin, y-globulin, and fibrinogen to become available for clinical use, was developed during World War II (see also Fractionation, blood-plasma fractionation). A stainless steel blood cell separation bowl, developed in the early 1950s, was the earhest blood cell separator. A disposable polycarbonate version of the separation device, now known as the Haemonetics Latham bowl for its inventor, was first used to collect platelets from a blood donor in 1971. Another cell separation rotor was developed to faciUtate white cell collections. This donut-shaped rotor has evolved to the advanced separation chamber of the COBE Spectra apheresis machine. [Pg.519]

Haemonetics Bowl Technology. Haemonetics disposable bowl technology has evolved from the original plasma separation chamber. The two principal shapes of bowls are the Latham bowl and the blow-molded bowl (Fig. 4). [Pg.522]

Fig. 4. Haemonetics disposable bowls (a) Latham bowl, and (b) blow-molded bowl. Fig. 4. Haemonetics disposable bowls (a) Latham bowl, and (b) blow-molded bowl.
Fig. 5. Separation in Latham bowl (a) whole blood is pumped down the feed tube and enters bowl at bottom (b) centrifugal force spins denser cellular components outside, leaving plasma or platelet-rich plasma (PRP) in inner band (c) when bowl is full, plasma flows out effluent tube, followed by platelets and then leukocytes, until bowl is almost completely full of ted cells (d) after draw is completed, bowl stops spinning and uncoUected components are... Fig. 5. Separation in Latham bowl (a) whole blood is pumped down the feed tube and enters bowl at bottom (b) centrifugal force spins denser cellular components outside, leaving plasma or platelet-rich plasma (PRP) in inner band (c) when bowl is full, plasma flows out effluent tube, followed by platelets and then leukocytes, until bowl is almost completely full of ted cells (d) after draw is completed, bowl stops spinning and uncoUected components are...
A small (25-kg), portable apheresis system, available in 1993, is designed to meet a wide variety of blood cell separation needs. The role of the apheresis system is to control the behavior, separation, and collection of blood components from the bowl while maintaining maximum donor safety. The system controls the flow rates of blood and components through variable pump speeds. It directs the flow of components out of the bowl, by fully automatic opening and closing of valves based on the output of the system sensors. The system monitors the separation of blood components in the bowl by an optics system that aims at the shoulder of the bowl. A sensor on the effluent line monitors the flow of components out of the bowl. [Pg.523]

The special design of the Latham bowl allows for a specific blood cell separation known as SURGE. This technique makes use of the principle of critical velocity. The Latham bowl is filled until the huffy coat, ie, layer of platelets and white cells, moves in front of the bowl optics. At this point the machine starts to recirculate plasma through the bowl at increasing rates. The smallest particles, ie, platelets, ate the first to leave the bowl. Their high number causes the effluent line to turn foggy. The optical density of the fluid in the effluent line is monitored by the line sensor. A special algorithm then determines when to open and close the appropriate valves, as well as the optimum recirculation rate. [Pg.523]

The unusual resiHence of ionomers combined with ease of processing have resulted in widespread replacement of balata mbber as golf-ball covers. In order to obtain desirable backspin characteristics, low glass-transition ionomer compositions have been developed (10). Transparent coatings on bowling pins promote both longer life and improved playing performance. [Pg.408]


See other pages where Bowl is mentioned: [Pg.73]    [Pg.885]    [Pg.474]    [Pg.2827]    [Pg.481]    [Pg.110]    [Pg.262]    [Pg.263]    [Pg.459]    [Pg.189]    [Pg.282]    [Pg.324]    [Pg.417]    [Pg.198]    [Pg.198]    [Pg.198]    [Pg.49]    [Pg.384]    [Pg.412]    [Pg.413]    [Pg.413]    [Pg.414]    [Pg.522]    [Pg.529]    [Pg.180]    [Pg.182]    [Pg.190]    [Pg.297]    [Pg.310]    [Pg.255]    [Pg.357]   
See also in sourсe #XX -- [ Pg.371 ]




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