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And sonicated

Composition and Methods of Manufacture. Vaccine is produced from the Oka attenuated strain. Vacciae is produced in human diploid cells such as MRC-5. After growth in the cell substrate, the cells themselves are harvested into the growth medium and sonicated to release the cell-associated vims. Sucrose and buffering salts are generally in the medium to help stabiLize the vims. The vacciae is presented in a free2e-dried vial to be reconstituted with sterile distilled water before injection (27). [Pg.358]

Step 2, Reuse the rotor tip speed and sonic velocity from Example 4-1 as the conditions used in their development that have not changed. [Pg.106]

These nested nanotubes may be harvested from the core by grinding and sonication nevertheless, substantial fractions of other types of carbon remain, all of which are capable of producing strong Raman bands... [Pg.137]

We need the porosity. R is given by R in the lower sand. We also need R. Ultrasonic Caliper and Sonic Log while Drilling... [Pg.993]

Glassy carbon electrodes polished with alumina and sonicated under clean conditions show activation for the ferrl-/ ferro-cyanlde couple and the oxidation of ascorbic acid. Heterogeneous rate constants for the ferrl-/ ferro-cyanlde couple are dependent on the quality of the water used to prepare the electrolyte solutions. For the highest purity solutions, the rate constants approach those measured on platinum. The linear scan voltammetrlc peak potential for ascorbic acid shifts 390 mV when electrodes are activated. [Pg.582]

Van Emon et al. ° developed an immunoassay for paraquat and applied this assay to beef tissue and milk samples. Milk was diluted with a Tween 20-sodium phosphate buffer (pH 7.4), fortified with paraquat, and analyzed directly. Fortified paraquat was detected in milk at less than 1 pgkg , a concentration which is considerably below the tolerance level of 10 pg kg Ground beef was extracted with 6 N HCl and sonication. Radiolabeled paraquat was extracted from ground beef with recoveries of 60-70% under these conditions. The correlation coefficient of ELISA and LSC results for the ground beef sample was excellent, with = 0.99, although the slope was 0.86, indicating a significant but reproducible difference between the assays. [Pg.698]

Extraction of neonicotinoid residues from soil is much more difficult than their extraction from plant or water samples. Soil residues could exist as bound residue . Various extraction methods such as organic solvent extraction, supercritical fluid extraction (SEE), Soxhlet extraction and sonication have been used. Some extraction methods are described in the following. [Pg.1139]

Weigh 30 g (dry soil base) of soil into a 300-mL round-bottom flask, add 90 mL of acetonitrile and 30 mL of water, shake the mixture for 10 min and sonicate it for 30 min. Filter the mixture through a Alter paper on a Buchner funnel by suction and collect the filtrate in a 500-mL round-bottom flask. Wash the beaker and the residue with 60 mL of acetone and filter the washings. Combine and concentrate the filtrates to 20 mL at 50 °C or lower under reduced pressure. [Pg.1193]

The extraction rate of mepanipyrim with refluxing was higher than that with shaking (30 min) and sonication (Ultrasonic, 600 W, 28 kHz, 30 min). For the solvent system, acetone and acetonitrile showed almost similar extraction efficiencies. Methanol was found to be a less effective extraction solvent. Mepanipyrim was unstable in the acidic solution and alkaline solution under reflux conditions at 80 °C. The extraction rate of mepanipyrim under these conditions decreased to about 50% and 20%, respectively. Therefore, neutral solution was used as the extraction solvent in this method. [Pg.1227]

Measure 50 mL of the filtrate into a 250-mL boiling flask and evaporate the filtrate aliquot to dryness under vacuum using a water-bath at 60 °C. Remove the boiling flask from the evaporator, add 25 mL of hexane to the flask, and sonicate the contents in a water-bath for 1 min. [Pg.1285]

Transfer the sample to the column and drain the solvent to the top of the sodium sulfate layer. Rinse the round-bottom flask three times with 3-mL portions of hexane, adding these rinses sequentially to the column and draining the solvent to the top of the sodium sulfate layer before the next addition. Pass 90 mL of hexane through the column, followed by 50 mL of hexane-diethyl ether (15 1, v/v). Add each portion of eluting solvent to the round-bottom flask and sonicate the flask before adding the solution to the column. Discard the accumulated eluate. Place a 250-mL round-bottom flask under the column and elute the pyriproxyfen residues with 50 mL of hexane-diethyl ether (15 1, v/v), followed by 20 mL of hexane-acetone (7 3, v/v). As before, add each portion of eluting solvent to the round-bottom flask and sonicate the flask before adding the solution to the column. Rotary evaporate the combined eluate under reduced pressure in a <40 °C water-bath to 40-50 mL. Transfer the sample to a 100-mL round-bottom flask with three 5-mL acetone rinses, and continue rotary evaporation to take the sample just to dryness. Reconstitute the sample in 1.0 mL of toluene with sonication for analysis (Section 6.2). [Pg.1345]

A detailed description of sources used in atmospheric pressure ionization by electrospray or chemical ionization has been compiled.2 Atmospheric pressure has been used in a wide array of applications with electron impact, chemical ionization, pressure spray ionization (ionization when the electrode is below the threshold for corona discharge), electrospray ionization, and sonic spray ionization.3 Interferences potentially include overlap of ions of about the same mass-charge ratio, mobile-phase components, formation of adducts such as alkali metal ions, and suppression of ionization by substances more easily ionized than the analyte.4 A number of applications of mass spectroscopy are given in subsequent chapters. However, this section will serve as a brief synopsis, focusing on key techniques. [Pg.59]

Extraction techniques for polymeric matrices can be divided into traditional and new . The traditional techniques include Soxhlet extraction, boiling under reflux, shaking extraction and sonication. All these methods are at atmospheric pressure. When the sample is added to a solvent, which is boiled under reflux (i.e. at the highest possible temperature without applying an external pressure) extractions tend to be much faster than Soxhlet extractions. Examples are the Soxtec ,... [Pg.59]

Brandt [200] has extracted tri(nonylphenyl) phosphite (TNPP) from a styrene-butadiene polymer using iso-octane. Brown [211] has reported US extraction of acrylic acid monomer from polyacrylates. Ultrasonication was also shown to be a fast and efficient extraction method for organophosphate ester flame retardants and plasticisers [212]. Greenpeace [213] has recently reported the concentration of phthalate esters in 72 toys (mostly made in China) using shaking and sonication extraction methods. Extraction and analytical procedures were carefully quality controlled. QC procedures and acceptance criteria were based on USEPA method 606 for the analysis of phthalates in water samples [214]. Extraction efficiency was tested by spiking blank matrix and by standard addition to phthalate-containing samples. For removal of fatty acids from the surface of EVA pellets a lmin ultrasonic bath treatment in isopropanol is sufficient [215]. It has been noticed that the experimental ultrasonic extraction conditions are often ill defined and do not allow independent verification. [Pg.80]

It is not uncommon that extraction techniques are unfairly compared. Appropriate interlaboratory studies are few. Soxhlet and sonication extraction (EPA methods 3540 and 3550, respectively) were compared in an interlaboratory study (129 participants) for PCBs in soil. Results from laboratories using Soxhlet extraction were significantly more accurate than those obtained using sonication, especially at higher concentrations, but with equal precision [196]. This is rationalised by the observation that the Soxhlet procedure presents the sample with fresh solvent so that the extraction solvent is never saturated, unlike the sonication procedure. Sonication is very sensitive to the solvent polarity, nonpolar solvents producing considerably less accurate results than polar solvents. It is not as sensitive to clean-up procedures as... [Pg.134]

The efficiencies of electrostatic precipitators, bag filters, and scrubbers are given in Figure 16-3. The costs for installing and operating these devices are given in reference 20. This source also describes some exotic methods, such as the use of thermophoretic or diffusiophorctic forces and sonic agglomeration, that have not yet been commercialized. [Pg.433]

Relationship Among Critical Discharge Rate, Pressure Propagation Rate, and Sonic Velocity... [Pg.9]

Hsu, Y. Y., 1972, Review of Critical Flow Rate, Propagation of Pressure Pulse, and Sonic Velocity in Two-Phase Media, NASA TN D-6814, NASA Lewis Res. Ctr, Cleveland, OH. (3)... [Pg.538]

Sadeghi, K. M. Sadeghi, M.-A. Kuo, J. F. Jang, L. K. Yen, T. F. Self-Propogated Surfactants Formed During Separation of Bitumen From Tar Sands Using an Alkaline Solution and Sonication, Presented at ACS, 1987 Pacific Conference on Chemistry and Spectroscopy, October 28-30, 1987. [Pg.407]

Air (particulate lead) Collection of particulate matter onto filter extraction with HN03/ HCI, heat, and sonication ICP/AES No data No data EPA 1988a... [Pg.452]

Chivate MM, Pandit AB (1993) Effect of hydrodynamic and sonic cavitation on aqueous polymeric solutions. Ind Chem Engr 35 52-57... [Pg.103]

Some of the reports are as follows. Mizukoshi et al. [31] reported ultrasound assisted reduction processes of Pt(IV) ions in the presence of anionic, cationic and non-ionic surfactant. They found that radicals formed from the reaction of the surfactants with primary radicals sonolysis of water and direct thermal decomposition of surfactants during collapsing of cavities contribute to reduction of metal ions. Fujimoto et al. [32] reported metal and alloy nanoparticles of Au, Pd and ft, and Mn02 prepared by reduction method in presence of surfactant and sonication environment. They found that surfactant shows stabilization of metal particles and has impact on narrow particle size distribution during sonication process. Abbas et al. [33] carried out the effects of different operational parameters in sodium chloride sonocrystallisation, namely temperature, ultrasonic power and concentration sodium. They found that the sonocrystallization is effective method for preparation of small NaCl crystals for pharmaceutical aerosol preparation. The crystal growth then occurs in supersaturated solution. Mersmann et al. (2001) [21] and Guo et al. [34] reported that the relative supersaturation in reactive crystallization is decisive for the crystal size and depends on the following factors. [Pg.176]

Arefian NA, Shokuhfar A, Vaezi MR, Kandjani AE, Tabriz MF (2008) Sonochemical synthesis of SnO/ZnO nano-Composite the effects of temperature and sonication power. In Ochsner A, Murch GE (eds) Defect and diffusion forum, vol 273-276, Diffusion in solids and liquids III., pp 34-39... [Pg.209]

In the study of effects of ultrasound on the aqueous reactions of nickel, we found some interesting results, for example, the colloidal formation of Ni-DMG complex and degassing of NH3 during different experiments. When 25 ml of 0.001 M NiSC>4 solution was complexed with 5 ml of 1% dimethyl glyoxime (DMG) in faintly alkaline ammonia medium and sonicated for 30 minutes and compared with another set of 25 ml of complexed solution which was stirred mechanically, a colloidal solution of Ni-DMG complex was formed in sonicated condition. Particles of Ni-DMG complex did not settle even after keeping 3 1 h because of their smaller size, in sonicated solution, whereas in the unsonicated condition large particles of Ni-DMG complex settled down immediately. [Pg.240]

In yet another experiment, three set of 25 ml of 100 ppm NiS04 solutions were complexed with 0.1 ml of 1% l-Nitroso-2-Naphthol and sonicated for 10, 20 and 30 min and compared with a control sample which was stirred mechanically. Turbidity of these solutions was measured. From the Table 9.9, it is clear that the turbidity of the solution increased as the time of sonication increased. [Pg.240]


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