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Limiting strips

Product Availability Limited Moderate Limited Limited Wide Moderate Limited, strip shops decreasing Moderate Moderate Long Long... [Pg.245]

Finally, there are some limits regarding LPG fuels butadiene content (0.5 wt. % maximum, ISO 7941), the absence of hydrogen sulfide (ISO 8819) and copper strip corrosion (class 1, ISO 6251) which are not usually problems for the refiner. [Pg.230]

Adsorptive stripping analysis involves pre-concentration of the analyte, or a derivative of it, by adsorption onto the working electrode, followed by voltanmietric iiieasurement of the surface species. Many species with surface-active properties are measurable at Hg electrodes down to nanoniolar levels and below, with detection limits comparable to those for trace metal detemiination with ASV. [Pg.1932]

Precision Precision is generally limited by the uncertainty in measuring the limiting or peak current. Under most experimental conditions, precisions of+1-3% can be reasonably expected. One exception is the analysis of ultratrace analytes in complex matrices by stripping voltammetry, for which precisions as poor as +25% are possible. [Pg.531]

Time, Cost, and Equipment Commercial instrumentation for voltammetry ranges from less than 1000 for simple instruments to as much as 20,000 for more sophisticated instruments. In general, less expensive instrumentation is limited to linear potential scans, and the more expensive instruments allow for more complex potential-excitation signals using potential pulses. Except for stripping voltammetry, which uses long deposition times, voltammetric analyses are relatively rapid. [Pg.531]

Fig. 1. Snamprogretti thermal stripping urea process. BL = battery limits. Fig. 1. Snamprogretti thermal stripping urea process. BL = battery limits.
Aniline Oxidation. Even though this is quite an old process, it still has limited use to produce hydroquinone on a commercial scale. In the first step, aniline is oxidized by manganese dioxide in aqueous sulfuric acid. The resulting benzoquinone, isolated by vapor stripping, is reduced in a second step by either an aqueous acidic suspension of iron metal or by catalytic hydrogenation. [Pg.487]

Extreme caution must be taken to prevent the possibility of fire when using flammable removers. Extra care must be taken when stripping on location to secure the area of ignition sources. When used on lacquer finishes, the dissolved finish and remover combined are extremely flammable. Natural mbber, neoprene, or other gloves suitable for use with the remover formula must be worn. The effect of skin contact with the remover is limited because there is immediate irritation and discomfort. Canister respirators are available for most petroleum and oxygenate remover solvents. Symptoms of long-term overexposure should be compared to symptoms of the major ingredients in the formula. [Pg.552]

Process water streams from vinyl chloride manufacture are typically steam-stripped to remove volatile organics, neutralized, and then treated in an activated sludge system to remove any nonvolatile organics. If fluidized-bed oxychlorination is used, the process wastewater may also contain suspended catalyst fines and dissolved metals. The former can easily be removed by sedimentation, and the latter by precipitation. Depending on the specific catalyst formulation and outfall limitations, tertiary treatment may be needed to reduce dissolved metals to acceptable levels. [Pg.419]

Attack on metals can be a function of fuel components as well as of water and oxygen. Organic acids react with cadmium plating and 2inc coatings. Traces of H2S and free sulfur react with silver used in older piston pumps and with copper used in bearings and brass fittings. Specification limits by copper and silver strip corrosion tests are requited for fuels to forestall these reactions. [Pg.416]

At the end of the 72-h cycle, the cathodes are removed from the cells, washed in hot water, and the brittie deposit, 3—6 mm thick, is stripped by a series of air hammers. The metal is then cmshed by roUs to 50-mm size and again washed in hot water. The metal contains about 0.034% hydrogen and, after drying, is dehydrogenated by heating to at least 400°C in stainless steel cans. Composition limits for electrolytic chromium are shown in Table 4. [Pg.118]


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