10. General Procedure for Kinematic Viscosity
10.1 Adjust and maintain the viscometer bath at the required test temperature within the limits given in 6.3.1 taking account of the conditions given in Annex A2 and of the corrections supplied on the certificates of calibration for the thermometers.
10.1.1 Thermometers shall be held in an upright position under the same conditions of immersion as when calibrated.
10.1.2 In order to obtain the most reliable temperature measurement, it is recommended that two thermometers with valid calibration certificates be used (see 6.4).
10.1.3 They should be viewed with a lens assembly giving approximately five times magnification and be arranged to eliminate parallax errors.

10.2 Select a clean, dry, calibrated viscometer having a range covering the estimated kinematic viscosity (that is, a wide capillary for a very viscous liquid and a narrower capillary for a more fluid liquid). The flow time for manual viscometers shall not be less than 200s or the longer time noted in Specifications D446. Flow times of less than 200s are permitted for automated viscometers, provided they meet the requirements of 6.1.2.
10.2.1 The specific details of operation vary for the different types of viscometers listed in Table A1.1. The operating instructions for the different types of viscometers are given in Specifications D446.
10.2.2 When the test temperature is below the dew point, fill the viscometer in the normal manner as required in 11.1. To ensure that moisture does not condense or freeze on the walls of the capillary, draw the test portion into the working capillary and timing bulb, place rubber stoppers into the tubes to hold the test portion in place, and insert the viscometer into the bath. After insertion, allow the viscometer to reach bath temperature, and the remove the stoppers. When performing manual viscosity determinations, do not use those viscometers which cannot be removed from the constant temperature bath for charging the sample portion.
10.2.2.1 The use of loosely packed drying tubes affixed to the open ends of the viscometer is permitted, but not required. If used, the drying tubes shall fit the design of the viscometer and not restrict the flow of the sample by pressures created in the instrument.
10.2.3 Viscometers used for silicone fluids, fluorocarbons, and other liquids which are difficult to remove by the use of a cleaning agent, shall be reserved for the exclusive use of those fluids except during their calibration. Subject such viscometers to calibration checks at frequent intervals. The solvent washings from these viscometers shall not be used for the cleaning of other viscometers.