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Bottle-point method

Equilibrium isotherms are generally done by the bottle-point method in which each bottle represents an equilibrium data point. Predetermined amounts of ground-up (60 x 100 mesh) adsorbent are added to bottles of raw water such that the final equilibrium arsenic concentration is within a specified range, which is generally between the influent concentration and one-half of the desired effluent concentration of arsenic. The bottles are capped, and then shaken or tumbled for 24-48 hr to achieve adsorption equilibrium. The final arsenic concentration in a filtered sample is determined and the loading on the adsorbent is calculated as the difference between the initial and final arsenic concentration divided by the mass of adsorbent. All points are replicated. Finally, a graph of arsenic loading qe, mg As/g adsorbent, is plotted vs. Ce, the mg As/L water. Isotherms are a rapid way to screen adsorbents on the basis of arsenic capacity under a variety of water-quality conditions. [Pg.229]

Bottled end-point method (applicable to acid-base, precipitation and redox titrations). In this method the reference electrode is replaced by a compensation electrode (figure P.12), the potential of which is exactly equal to that of the indicator electrode in the solution under titration at the end-point (previously determined). Electrodes reversible to one of the ions in the titration are coupled through a galvanometer so that the end-point is indicated by a sudden reversal of... [Pg.205]

Method A. Weigh out accurately about 3.5 g of potassium cyanide from a glass-stoppered weighing bottle, dissolve it in water and make up to 250 mL in a graduated flask. Shake well. Transfer 25.0 mL of this solution by means of a burette and NOT a pipette to a 250 mL conical flask, add 75 mL water, 5-6 mL 6M ammonia solution, and 2 mL 10 per cent potassium iodide solution. Place the flask on a sheet of black paper, and titrate with standard 0.1 M silver nitrate. Add the silver nitrate solution dropwise as soon as the yellow colour of silver iodide shows any signs of persisting. When one drop produces a permanent turbidity, the end-point has been reached. [Pg.358]

The freezing of liquids in vials, bottles or flasks in a liquid bath is the most common freezing method used in laboratories. As the liquid must have a low melting point, alcohol (ethanol, melting point -114 °C) cooled by C02 (boiling point -80 °C at 1 atm) is frequently used. The bath can also be cooled by refrigerated coils. [Pg.127]

Several points need to be considered when applying this pressure method of sample collection. All of the extraction system parts must be explosion proof and the distance from the ceramic cup to the sample bottle must be as short as possible. The sample collection bottle should be at the same level as the ceramic cup. If it is higher, additional vacuum will need to be applied to move the sample water into the sample bottle. Sample storage, once the water is collected, is determined by the analyte of interest. [Pg.231]

A sample of the sieved particles was also devulcanized by the phenyllithium method (4). An oven-dried 200 mL beverage bottle was charged with 1 g of 18-60 mesh particles and 40 mL of dry benzene. The bottle was capped with a 1-hole cap (extracted neoprene liner) and 10 mL of 2 M phenyllithium added. The mixture was shaken for 6.5 h at room temperature, then 1.5 mL of methanol added. Finally, 4 mL of methyl iodide was injected. At thi point the mixture comprised a rubber solution and a suspension of salts. An aliquot of the solution was taken for gpc analysis. [Pg.165]

We point out here that the colloid prepared by these methods is very clean, because the carrier gas used is usually high-purity grade at six-nine, the chamber is once evacuated to depress the extent of contaminating oxygen and moisture, and the liquids themselves are always purified by sublimation process except for the solution trap method. To transfer the colloidal suspension after preparation, a specially designed stock bottle with a Luer-lock syringe is normally used in order to enable the operations under Ar flow to avoid unexpected air contamination. Therefore, we can carry the suspension liquid away from the production chamber without exposure to air, which means that the surface of colloidal metal is very clean if it does not react with suspension liquids. [Pg.523]

Fruit juices and unfilterable drinks. Spht bottle method. Action points ... [Pg.290]


See other pages where Bottle-point method is mentioned: [Pg.41]    [Pg.41]    [Pg.320]    [Pg.41]    [Pg.230]    [Pg.791]    [Pg.305]    [Pg.447]    [Pg.282]    [Pg.454]    [Pg.125]    [Pg.230]    [Pg.791]    [Pg.901]    [Pg.454]    [Pg.350]    [Pg.277]    [Pg.14]    [Pg.92]    [Pg.28]    [Pg.50]    [Pg.134]    [Pg.129]    [Pg.152]    [Pg.62]    [Pg.80]    [Pg.305]    [Pg.306]    [Pg.408]    [Pg.408]    [Pg.230]    [Pg.791]    [Pg.194]    [Pg.363]    [Pg.729]    [Pg.740]    [Pg.126]    [Pg.29]    [Pg.444]    [Pg.7]    [Pg.285]   
See also in sourсe #XX -- [ Pg.41 ]




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