FEEDS 147 water as otherwise various substances, soluble in water or alcohol (salts, sugars and amids) would be extracted. Certain other fat solvents have been used, such as benzol, gasoline and carbon tetrachloride, but none has been found to be quite as satisfactory as dry ether. One form of assembled extraction apparatus is shown in Fig. 41. Any number of separate pieces may be assembled upon one heater. In Fig. 41 the third extractor is shown in section. Ether (or other volatile solvent) is placed in the weighed cup a where it boils and the condensed vapor from, the condenser d falls to the sample in the porous cup 6. As the solvent fills the siphon cup c to the level of the siphon bend, the cup automatically empties into a, below. This process repeats itself indefinitely. Determination, of Crude Fat.—Wash commercial ether by shaking in a separatory funnel with two or three successive portions of water and drawing off and discarding the latter. Add solid sodium or potassium hydroxide and let stand until most of the water has been abstracted from the ether. Decant into a dry bottle, add small pieces of cleaned metallic sodium or sodium wire, freshly extruded from a sodium press, and let stand until there is no further evolution of hydrogen. Keep the ether, thus dehy- drated, over metallic sodium in lightly stoppered bottles. The sample is thoroughly dried at 100° in an alundurn cup or fat-free paper capsule (or the sample used for the moisture determination is taken), then placed in an extracting tube and sufficient ether, as above prepared, is added to the weighed cup a of Fig. 41 (previously cleaned, dried and weighed) to enable continuous extraction to proceed automatically. The alundum cup is a porous vessel, cylindrical in shape, and convenient to use because it is easily cleaned by burning, so that it may be used repeatedly. It is suitable to use also in fiber filtration, as it permits weighing and burning of the fiber without removal to another vessel The porous alundum cup, grade R. A. 98, permits rapid filtering and washing. Extract the sample for sixteen hours, saving the residue for the fiber determination (page 148), then remove the cup a and allow the ether to evaporate, or place the cup in a special apparatus for distilling and recovering the ether. Dry at 100° for 30 minutes, cool in a desiccator and weigh. Repeat the drying for 30-minute periods until the weight is constant. From the difference between the weights before and after extraction, calculate the per cent of crude fat. Crude Fiber.—The so-called "crude fiber" is a mixture of substances which make up the framework of a plant. It is composed of cellulose, part of the hemi cellulose and lignin of the