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Residues, concentration

Pharmaceutical Industry. In the pharmaceutical industry, sterility of deionized water systems is maintained by using an ozone residual. The ozone residual concentration is maintained at >0.3 ppm ppm in the water recirculation loop. Prior to product compounding, the ozone residual is removed by contact with uvirradiaton for <1 s. Ozone also is used to oxidize pyrogens from distilled water destined for intravenous solutions. [Pg.502]

Sodium alumiaate is used ia the treatment of iadustrial and municipal water suppHes and the use of sodium alumiaate is approved ia the clarification of drinking water. The FDA approves the use of sodium alumiaate ia steam generation systems where the steam contacts food. One early use of sodium alumiaate was ia lime softening processes, where it iacreases the precipitation of ions contributing to hardness and improves suspended soHds removal from the treated water (17). Sodium alumiaate reacts with siHca to leave very low residual concentrations of siHca ia hot process water softeners. Sodium alumiaate is often used with other chemicals such as alum, ferric salts, clays, and polyelectrolytes, as a coagulant aid (18,19). [Pg.140]

After epoxidation a distillation is performed to remove the propylene, propylene oxide, and a portion of the TBHP and TBA overhead. The bottoms of the distillation contains TBA, TBHP, some impurities such as formic and acetic acid, and the catalyst residue. Concentration of this catalyst residue for recycle or disposal is accompHshed by evaporation of the majority of the TBA and other organics (141,143,144), addition of various compounds to yield a metal precipitate that is filtered from the organics (145—148), or Hquid extraction with water (149). Low (<500 ppm) levels of soluble catalyst can be removed by adsorption on soHd magnesium siUcate (150). The recovered catalyst can be treated for recycle to the epoxidation reaction (151). [Pg.139]

Provisions must be made for allowing residues of the stefilant absorbed by the product to dissipate by using aeration cabinets that have forced-air circulation at elevated temperatures. The amount of remaining absorbed stefilant should be determined before releasing the sterilized articles. If, as in the case of hospital sterilization, such studies are not feasible, the recommendations of the manufacturers of the articles sterilized or of the aeration equipment should be obtained. The permissible residue concentrations are 10—250 ppm, depending on the type of article and on its intended use. [Pg.409]

Water Treatment. Sodium sulfite is an agent in the reduction of chlorine or oxygen in water. Dissolved oxygen in boiler water tends to enhance pitting and other types of corrosion. In boilers operated at below 4.82 MPa (700 psi), a residual concentration of 30 ppm of sodium sulfite is generally effective. Catalytic amounts of cobalt are often added to accelerate the reaction of oxygen with sulfite (321,322) (see Water, industrial water treatment). [Pg.149]

Inorganic heavy metals are usually removed from aqueous waste streams by chemical precipitation in various forms (carbonates, hydroxides, sulfide) at different pH values. The solubiUty curves for various metal hydroxides, when they are present alone, are shown in Figure 7. The presence of other metals and complexing agents (ammonia, citric acid, EDTA, etc) strongly affects these solubiUty curves and requires careful evaluation to determine the residual concentration values after treatment (see Table 9) (38,39). [Pg.228]

Table 9. Typical Residual Concentrations after Chemical Precipitation ... Table 9. Typical Residual Concentrations after Chemical Precipitation ...
In wooden tubs, the maintenance of a sanitizer residual becomes compHcated due to the leaching of tannins and other organic matter from the wood into the water. The sanitizer demand of these substances must be overcome in order to maintain proper residual concentrations. As the tub ages, the leaching of these materials decreases, but bleaching of the wood may occur as the lignin (qv) in the wood reacts with sanitizers. [Pg.303]

Pulp bleaching with chlorine dioxide is most often performed at an acidic pH, so that the final pH of the bleach Hquor is in the range of 2—5. Under these conditions, the residual concentration of chlorite and chlorate ions in the bleach Hquor are minimized and chloride ion is the predominant chlorine species in the spent bleach (77). In addition to direct addition to pulp in bleaching, chlorine dioxide also finds use in wastewater treatment from pulp mill operations as a means to remove effluent color (85). [Pg.484]

The effluent concentration history is the breakthrough curve, also shown in Fig. 16-3. The effluent concentration stays at or near zero or a low residual concentration until the transition reaches the column outlet. The effluent concentration then rises until it becomes unacceptable, this time being called the breakthrough time. The feed step must stop and, for a regenerative system, the regeneration step begins. [Pg.1499]

The escaping bubbles from the top of a bubble-fractionation column can carry off an appreciable quantity of adsorbed material in an aerosol of very fine film drops [various papers, J. Geophys. Res., Oceans Atmos., 77(27), (1972)]. If the residu solute is thus appre-ciablv depleted, Cj in Eq. (22-57) should be replaced with the average residual concentration. [Pg.2022]

In a binaiy separation, the highest purity of integrated permeate occurs at 0 = 0. Purity decreases monotonicaUy until it reaches the feed purity at 0 = 1. In a ternary system, the residue concentration of the gas with the intermediate permeabihty will reach a maximum at some intermediate stage cut. [Pg.2052]

FIG. 23-15 Chemical conversion by the dispersion model, (a) First-order reaction, volume relative to plug flow against residual concentration ratio, (h) Second-order reaction, residual concentration ratio against kC t. [Pg.2090]

As the organic or volatile material is reduced due to the batch distillation, the steam pressure rises during the progress of the operation due to the loss of the volatile material, and the decrease of pim- When the volatile material is stripped down to a low residual concentration, then Ps approaches the total system pressure, n. When the steam saturation pressure and temperature is greater than 7t, no steam condensation will occur during the operation. [Pg.59]

The fluorescence quenching depends on the content of the Phen units (the x values) in APh-x. An aqueous solution of APh-9 contained as many charged groups (SOJ) as about 10 times that of APh-50, when compared at the same molar concentration of the Phen residues. When AMPS homopolymer (PAMPS) was added to a solution of APh-50 so that the SOJ residue concentration was equal to that for APh-9, the kq value for the APh-50 quenching by MV2 + decreased from 2.1 x 1012 to 4.2 x 1011 M-1 s 1, which is close to the kq value for APh-9 (Table 2). From these facts the lower kq values for APh-x with lower x (higher... [Pg.71]

The second reason is of kinetic nature and due to a substantially lower reactivity of the pendant acrylic groups. Some experimental facts may be considered a direct evidence of this possibility. Thus, the absorption in the region of 280 nm in the UV spectrum points to a growth of the residual concentration of acrylamide groups with an increasing fraction of the crosslinker [25]. The same groups can... [Pg.102]

In field trials following multiple aerial applications of endosulfan for tsetse fly control in Africa over a 3-month period, residues of the compound in fish tissues decreased to low concentrations within 3 months after spraying. The fish tissue residues were still detectable after 12 months. Residue concentrations in fish-eating birds and crocodiles were similar to fish tissue residue levels endosulfan did not biomagnify in the food chain (HSDB 1999). [Pg.228]

Reliable analysis of endosulfan residue concentrations in environmental samples usually involves detection of the a- and p-isomers plus endosulfan sulfate (a degradation product of endosulfan). [Pg.250]

Carey AE, Douglas P, Tai H, et al. 1979a. Pesticide residue concentrations in soils of five United States cities, 1971-Urban Soils Monitoring Program. Pestic Monit J 13 17-22. [Pg.279]

The problem asks for the residual concentration of cadmium ions. In other words, what is the Cd ion concentration in the solution after the NaOH is added Before a concentration table can be completed,... [Pg.1314]

Notice that virtually all the mass that dissolved originally (Example ) has been recovered, and the residual concentration of Cd " is veiy small. Both these observations are consistent with a water treatment process. [Pg.1315]

Extraction procedures must be adjusted when separated anthocyanins will be tested in biological studies. We have found that the types of acids used for anthocyanin extraction as well as their residual concentrations in the final extract may affect the results obtained from biological tests. The growth inhibitory effect of anthocyanins on HT29 (human colonic cancer) cells may be overestimated if the residual acid in the extract exerts a toxic effect on the cells. Acetic acid residues in anthocyanin extracts showed less toxicity to HT29 cells than hydrochloric acid when samples were prepared under the same extraction procedure and subjected to the same tests on HT29 cells. In addition, the procedure to remove acids affected the acid residual concentration as well in final anthocyanin extracts, with lyophilization being more successful than rotary evaporation. [Pg.482]

Accurate monitoring of inhibitor residual concentrations is most important in systems in which the volume of water is unknown or is highly variable. Frequent monitoring of the inhibitor concentration in the water exiting the pipeline is the simplest method, and sometimes the only method that can be used, to ensure that the line in fact is being protected. [Pg.86]

The next step requires the determination of the residual concentrations C by subtracting from the observed Cp. The resulting a-phase function is again obtained by means of linear regression on the earlier part of the time course of the logarithmic plasma concentration (Fig. 39.13b) ... [Pg.481]


See other pages where Residues, concentration is mentioned: [Pg.24]    [Pg.291]    [Pg.405]    [Pg.149]    [Pg.228]    [Pg.285]    [Pg.303]    [Pg.348]    [Pg.292]    [Pg.58]    [Pg.241]    [Pg.1441]    [Pg.148]    [Pg.239]    [Pg.48]    [Pg.18]    [Pg.142]    [Pg.217]    [Pg.877]    [Pg.269]    [Pg.1314]    [Pg.1315]    [Pg.199]    [Pg.212]    [Pg.397]    [Pg.35]   
See also in sourсe #XX -- [ Pg.850 ]




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