Simultaneous stripping

Rittstieg, K., Robra, K.H., and Somitsch, W., Aerobic treatment of a concentrated urea wastewater with simultaneous stripping of ammonia, Appl. Microbiol. Biotechnol., 56, 820-825, 2001. 

The stripping performances of Bi film on glassy carbon or carbon fiber substrates were examined very carefully by Wang et al. [17]. In addition to these materials, GECE (combined with bismuth film), a very easy to prepare and low-cost electrode, can also be used successfully for simultaneous stripping analysis of cadmium and lead. Zinc was also tried to be detected simultaneously with lead and cadmium but it was not possible to obtain undistorted and linearly increased peaks. The poor response to zinc can be probably attributed to the preferable accumulation of Bi on GECE rather than of Zn which is a result of the competition of these two metals for the GECE surface sites as also observed in other works [18]. 

Figure 13.1 represents schematically different types of HLM contactors. A liquid membrane solution flows (or circulates) between two membranes, which separate the LM phase (E) from the feed (F) and receiving (R) phases. A solute (or solutes) diffuses to the F/E interface and is extracted from feed phase by a carrier as a result of the thermodynamic conditions at the F/E interface. The solute-carrier complex diffuses to the E/R interface and is simultaneously stripped by the receiving phase due to the different thermodynamic conditions at the E/R interface. The membranes may be hydrophobic, immersed by LM, or hydrophilic (or ion exchange), immersed by feed and strip aqueous phases. 

In a normal newly constructed refining plant, the wedge type stripping machine (fixed type) can be utilized more effectively than the movable type. However, in an old facility like the Kamioka plant, the general layout is not suited for systemized mechanization and the wedge type (fixed type) stripping machine is not well utilized. Therefore, the Kamioka plant developed a movable multi-sheet simultaneous stripping machine in 1981 and used it imtil 1993. The outline of this machine is described below. 

Anodic-stripping voltaimnetry (ASV) is used for the analysis of cations in solution, particularly to detemiine trace heavy metals. It involves pre-concentrating the metals at the electrode surface by reducmg the dissolved metal species in the sample to the zero oxidation state, where they tend to fomi amalgams with Hg. Subsequently, the potential is swept anodically resulting in the dissolution of tire metal species back into solution at their respective fomial potential values. The detemiination step often utilizes a square-wave scan (SWASV), since it increases the rapidity of tlie analysis, avoiding interference from oxygen in solution, and improves the sensitivity. This teclmique has been shown to enable the simultaneous detemiination of four to six trace metals at concentrations down to fractional parts per billion and has found widespread use in seawater analysis. 

Figure 2 illustrates the three-step MIBK process employed by Hibernia Scholven (83). This process is designed to permit the intermediate recovery of refined diacetone alcohol and mesityl oxide. In the first step acetone and dilute sodium hydroxide are fed continuously to a reactor at low temperature and with a reactor residence time of approximately one hour. The product is then stabilized with phosphoric acid and stripped of unreacted acetone to yield a cmde diacetone alcohol stream. More phosphoric acid is then added, and the diacetone alcohol dehydrated to mesityl oxide in a distillation column. Mesityl oxide is recovered overhead in this column and fed to a further distillation column where residual acetone is removed and recycled to yield a tails stream containing 98—99% mesityl oxide. The mesityl oxide is then hydrogenated to MIBK in a reactive distillation conducted at atmospheric pressure and 110°C. Simultaneous hydrogenation and rectification are achieved in a column fitted with a palladium catalyst bed, and yields of mesityl oxide to MIBK exceeding 96% are obtained. 

Uranium Purification. Subsequent uranium cycles provide additional separation from residual plutonium and fission products, particularly zirconium— niobium and mthenium (30). This is accompHshed by repeating the extraction/stripping cycle. Decontamination factors greater than 10 at losses of less than 0.1 wt % are routinely attainable. However, mthenium can exist in several valence states simultaneously and can form several nitrosyl—nitrate complexes, some for which are extracted readily by TBP. Under certain conditions, the nitrates of zirconium and niobium form soluble compounds or hydrous coUoids that compHcate the Hquid—Hquid extraction. SiUca-gel adsorption or one of the similar Hquid—soHd techniques may also be used to further purify the product streams. 

The reactor effluent is rapidly quenched with aqueous mother Hquor in specially designed equipment operating at pressures essentially equal to the reactor pressure. This operation yields an off-gas consisting of ammonia and carbon dioxide vapor and a crystalline melamine slurry saturated with ammonia and carbon dioxide. The slurry is concentrated in a cyclone mill. The mother Hquor overflow is returned to the quenching system. The concentrated slurry is redissolved in the mother Hquor of the crystallization system, and the dissolved ammonia is stripped simultaneously. 

Suspension Polymerization. This method (10) might be considered as a number of bulk polymerizations carried out simultaneously in the monomer droplets with water acting as a heat-transfer medium. A monomer-soluble initiator, eg, a peroxide or azo compound, and a protective coUoid like poly(vinyl alcohol) or bentonite, are requited. After completion of the polymerization, the excess of monomer(s) is steam stripped, and the beads of polymer are collected and washed on a centrifiige or filter and dried on a vibrating screen or by means of an expeUer—extmder. 

A novel sensitive and seleetive adsorptive stripping proeedure for simultaneous determination of eopper, bismuth and lead is presented. The method is based on the adsorptive aeeumulation of thymolphetalexone (TPN) eomplexes of these elements onto a hanging mereury drop eleetrode, followed by reduetion of adsorbed speeies by voltammetrie sean using differential pulse modulation. The optimum analytieal eonditions were found to be TPN eoneentration of 4.0 p.M, pH of 9.0, and aeeumulation potential at -800 mV vs. Ag/AgCl with an aeeumulation time of 80 seeonds. The peak eurrents ai e proportional to the eoneentration of eopper, bismuth and lead over the 0.4-300, 1-200 and 1-100 ng mL ranges with deteetion limits of 0.4, 0.8 and 0.7 ng mL respeetively. The proeedure was applied to the simultaneous determination of eopper, bismuth and lead in real and synthetie samples with satisfaetory results. 

Net-tension failures can be avoided or delayed by increased joint flexibility to spread the load transfer over several lines of bolts. Composite materials are generally more brittle than conventional metals, so loads are not easily redistributed around a stress concentration such as a bolt hole. Simultaneously, shear-lag effects caused by discontinuous fibers lead to difficult design problems around bolt holes. A possible solution is to put a relatively ductile composite material such as S-glass-epoxy in a strip of several times the bolt diameter in line with the bolt rows. This approach is called the softening-strip concept, and was addressed in Section 6.4. 

Mesospheric sodium atoms excited at the 3Ps/2 level scatter light in every direction. The backscattered beam observed at an auxiliary telescope B meters away from the main one looks like a plume strip with an angular length (p B 8h / where 8h stands for the thickness of the sodium layer. The tilt of the wavefront at the auxiliary telescope and vibrations equally affects the plume and the NGS. Thus departures of the plume from the average NGS location is due to the only tilt on the upward laser beam. Therefore measuring this departure allows us to know the actual location of the LGS, and to derive the tdt. Because of Earth rotation and of perspective effects, the auxiliary telescope has to track the diurnal rotation, and simultaneously to move on the ground to keep aligned the NGS and the LGS plume. Two mobile auxiliary telescopes are necessary for the two components of the tilt. 

Since different metals strip from mercury electrodes at characteristic peak potentials, several metal ions can be determined simultaneously. Metal ions which have been determined by ASV at a mercury electrode are BP, Cd, Cu, Ga, Ge, In, NP, Pb, Sb, Sn, Tl, and Zn. Solid electrodes such as graphite enable Hg, Au, Ag, and PP to be determined by ASV. In this case, the metal is preconcentrated on the surface of the electrode as a metallic film, which is then stripped off by the positive potential scan. 

The intriguing observation that voltammetric CO stripping disappears at a certain Ru coverage, but the spectra from Ru-CO and Pt-CO patches are still measured at high Ru coverage, will now be considered. It can be seen that three conditions must be met simultaneously to obtain avoltammetric split of the type in Fig. 12.18 ... 

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