ASTM D5349-95(2001)
(Test Method)Standard Test Method for Determination of the Moisture and Volatile Content of Sulfonated and Sulfated Oils by Hot-Plate Method
Standard Test Method for Determination of the Moisture and Volatile Content of Sulfonated and Sulfated Oils by Hot-Plate Method
SCOPE
1.1 This test method covers the determination of the percentage of water and other compounds volatile at about 100°C existing in a sample of sulfonated or sulfated oil, or both, by rapid evaporation. This test method is applicable only to sulfonated and sulfated oils that do not contain the following: mineral acids, free sulfonic acids or free sulfuric acid esters, ammonia, acetic acid or similar volatile acids, alkali hydroxides, carbonates, acetates or similar salts that may react with oleic acid at elevated temperatures liberating volatile acids, or glycerin, diethylene glycol, xylene, or other compounds of similar volatility. This test method was derived from Test Methods D500, Sections 10 through 14.
1.2 The values stated in SI units are to be regarded as the standard.
1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use.
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Designation:D5349–95 (Reapproved 2001)
Standard Test Method for
Determination of the Moisture and Volatile Content of
Sulfonated and Sulfated Oils by Hot-Plate Method
This standard is issued under the fixed designation D 5349; the number immediately following the designation indicates the year of
original adoption or, in the case of revision, the year of last revision. A number in parentheses indicates the year of last reapproval. A
superscript epsilon (e) indicates an editorial change since the last revision or reapproval.
1. Scope 4.1.1 Weighing Flasks, any suitable glass-stoppered weigh-
ing flask of 10 to 15-mL capacity.
1.1 This test method covers the determination of the per-
4.1.2 Beaker, Griffin low-form glass beaker with an ap-
centage of water and other compounds volatile at about 100°C
proximate capacity of 150 mL and a diameter of about 5 cm.
existing in a sample of sulfonated or sulfated oil, or both, by
4.1.3 Heat Source—The source of heat may be either an
rapid evaporation. This test method is applicable only to
electrichotplatewithorwithoutasbestospaperorboardcover,
sulfonated and sulfated oils that do not contain the following:
or an open flame under a suitable asbestos board and a wire
mineral acids, free sulfonic acids or free sulfuric acid esters,
gauze (to spread the heat).
ammonia, acetic acid or similar volatile acids, alkali hydrox-
4.1.4 Thermometer, graduated from 90 to 150°C, about 3 in.
ides, carbonates, acetates or similar salts that may react with
in length, and substantially constructed.
oleic acid at elevated temperatures liberating volatile acids, or
glycerin, diethylene glycol, xylene, or other compounds of
5. Reagents
similar volatility. This test method was derived from Test
5.1 DesiccatingAgent—Any suitable desiccating agent may
Methods D 500, Sections 10 through 14.
be used.
1.2 The values stated in SI units are to be regarded as the
standard.
NOTE 1—Recent investigations seem to indicate that calcium chloride
1.3 This standard does not purport to address all of the is unreliable as a laboratory desiccating agent.
safety concerns, if any, associated with its use. It is the
5.2 Oleic Acid.
responsibility of the user of this standard to establish appro-
priate safety and health practices and determine the applica- 6. Procedure
bility of regulatory limitations prior to use.
6.1 Weigh approximately5gof oleic acid into the beaker
and insert the thermometer. Heat the oleic acid gradually, while
2. Referenced Documents
stirring with the thermometer, until the temperature reaches
2.1 ASTM Standards:
130°C. Place the beaker in an oven at 105 to 100°C for 15 min,
D 500 Test Methods of Chemical Analysis of Sulfonated
cool in a desiccator, and weigh. Repeat the heating over the hot
and Sulfated Oils
plate and in the oven until two successive weighings differ by
less than 1.5 mg.
3. Significance and Use
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