Residue-supernatant

Thermophilic treatment at 50°C left a higher residual supernatant BOD5 than that from similar mean treatment times but lower reaction temperatures (15). However, odour panel assessments of samples from a thermophilic reactor showed a similar relationship between odour and mean treatment time to that provided by equation 9, despite the slightly higher supernatant BOD5, (unpublished). This apparent contradiction is probably due to the logarithmic nature of the relationship and the small number of samples from thermophilic treatment, compared with the number from lower temperature treatment. 

Other words and expressions system, homogeneous, heterogeneous, phase, precipitate, filtrate, residue, supernatant liquid, centrifuge, supercentriiuge, emulsion, separatory funnel, still, condenser, receiver, distillate, gaseous solution, liquid solution, crystalline solution (solid solution), alloy, components. 

Centrifuge the precipitated phage at 4 °C for 15 min at 10,000 x. Decant the supernatant and briefly centrifuge the tube. Remove residual supernatant with a small pipette. 

Decant as much supernatant as possible, brie re-sjm the tubes, ai remove residual supernatant with a pipette. Resuspoid each phage pellet in 1 ml of IE and pool the ph e to give a 10 ml phage stock. 

Keywords Fly ash Hopper ash Lagoon ash Alkali activation Hydrothermal Fusion Grinding Residues Supernatant Characteristics ZeoUtization... 

While the diazotisation is in progress, cautiously add 165 ml. of concentrated sulphuric acid to 150 ml. of water in a 1-litre round-bottomed flask. Heat the mixture just to boiling. Add the supernatant Uquid (diazonium solution) from a separatory funnel supported over the flask at such a rate that the mixture boils very vigorously (about 30 minutes). Then add the residual damp soUd (or suspension) in small portions avoid excessive frothing. When aU the diazonium salt has been introduced, boil for a further 5 minutes and pour the mixture into a 1-Utre beaker... 

Murexide Indicator. Suspend 0.5 g of powdered murexide in water, shake thoroughly, and allow the undissolved solid to settle. Use 5-6 drops of the supernatant liquid for each titration. Decant the old supernatant liquid daily and treat the residue with water to provide a fresh solution of the indicator. 

When the overflow clarity is independent of overflow rate and depends only on detention time, as in the case for high soHds removal from a flocculating suspension, the required time is deterrnined by simple laboratory testing of residual soHd concentrations in the supernatant versus detention time under the conditions of mild shear. This deterrnination is sometimes called the second-order test procedure because the flocculation process foUows a second-order reaction rate. 

Clean sodium (0.19 g), free of paraffin or petroleum residues, is dissolved in deuterium oxide (1.2 ml) and Raney nickel alloy (0.25 g) is added in small portions over 8 min while maintaining the temperature at about 50°. When the addition is complete, the supernatant is poured off and the catalyst is washed by decantation with deuterium oxide (3x2 ml) followed by methanol-OD (2x1 ml). The catalyst should be prepared fresh as needed and the preparation carried out as rapidly as possible. 

A total of 50 ml (0.15 moles) of a 3 ethereal solution of methylmagnesium bromide is added slowly to a vigorously stirred solution of 5.8 g (12.5 mmoles) or 3,3 20,20-bisethylenedioxy-5a,6a-epoxy-5a-pregnane-ll/l,17a,21-triol in 400 ml of tetrahydrofuran. The solution is heated under reflux for 24 hr, cooled and treated with 32 ml of saturated ammonium chloride solution. The supernatant is decanted and the residue is washed with several portions of tetrahydrofuran. The combined supernatants are evaporated and extracted with ethyl acetate, washed with saturated salt solution, dried and concentrated to give 4,55 g (75%) of 3,3 20,20-bisethylenedioxy-6 -methyl-5a-pregnane-5a,ll, 17a,21-tetrol mp 170-172° after crystallisation from acetone-petroleum ether. The analytical sample is crystallized from acetone-petroleum ether mp 175-177° [aJo —11° (CHCI3). 

A mixture consisting of 0.69 g (10.5 mmoles) of zinc-copper couple, 12 ml of dry ether, and a small crystal of iodine, is stirred with a magnetic stirrer and 2.34 g (0.7 ml, 8.75 mmoles) of methylene iodide is added. The mixture is warmed with an infrared lamp to initiate the reaction which is allowed to proceed for 30 min in a water bath at 35°. A solution of 0.97 g (2.5 mmoles) of cholest-4-en-3/ -ol in 7 ml of dry ether is added over a period of 20 min, and the mixture is stirred for an additional hr at 40°. The reaction mixture is cooled with an ice bath and diluted with a saturated solution of magnesium chloride. The supernatant is decanted from the precipitate, and the precipitate is washed twice with ether. The combined ether extracts are washed with saturated sodium chloride solution and dried over anhydrous sodium sulfate. The solvent is removed under reduced pressure and the residue is chromatographed immediately on 50 g of alumina (activity III). Elution with benzene gives 0.62 g (62%) of crystalline 4/5,5/5-methylene-5 -cholestan-3/5-ol. Recrystallization from acetone gives material of mp 94-95° Hd -10°. 

When the entire quantity of the phosphoric acid has thus been added, agitation of the mixture is continued for about a half-hour or more to insure complete conversion. The precipitate is then allowed to settle, the supernatant liquid is drawn off, and the residue is filtered. The precipitate thus separated may, if desired, be washed with acetone and is then dried by evaporation to constant weight. It forms a fine, white, impalpable powder consisting of pure monobasic amphetamine phosphate. 

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